2,38c2,21
< "5310","glycogen-rich clear cell breast carcinoma","umls","C0334319"
< "5310","glycogen-rich clear cell breast carcinoma","umls","C1512224"
< "5310","glycogen-rich clear cell breast carcinoma","mondo","0003390"
< "2012","Nezelof syndrome","icd10cm","D81.4"
< "2012","Nezelof syndrome","icd9cm","279.13"
< "2012","Nezelof syndrome","mesh","C536288"
< "2012","Nezelof syndrome","umls","C0152094"
< "2012","Nezelof syndrome","mondo","0009451"
< "13736","uterine inflammatory disease","icd10cm","N71.9"
< "13736","uterine inflammatory disease","icd9cm","615.9"
< "13736","uterine inflammatory disease","umls","C0269047"
< "13736","uterine inflammatory disease","mondo","0001786"
< "4024","scirrhous adenocarcinoma","mesh","D002293"
< "4024","scirrhous adenocarcinoma","umls","C0007135"
< "4024","scirrhous adenocarcinoma","mondo","0005953"
< "0070070","autosomal dominant non-syndromic intellectual disability 40","mondo","0014699"
< "12385","shigellosis","kegg","05131"
< "12385","shigellosis","icd10cm","A03"
< "12385","shigellosis","icd10cm","A03.0"
< "12385","shigellosis","icd10cm","A03.1"
< "12385","shigellosis","icd10cm","A03.2"
< "12385","shigellosis","icd10cm","A03.9"
< "12385","shigellosis","icd9cm","004"
< "12385","shigellosis","icd9cm","004.0"
< "12385","shigellosis","icd9cm","004.1"
< "12385","shigellosis","icd9cm","004.2"
< "12385","shigellosis","icd9cm","004.9"
< "12385","shigellosis","mesh","D004405"
< "12385","shigellosis","umls","C0013371"
< "12385","shigellosis","umls","C0302358"
< "12385","shigellosis","umls","C0302359"
< "12385","shigellosis","umls","C0302360"
< "12385","shigellosis","mondo","0019345"
< "2917","cryoglobulinemia","icd10cm","D89.1"
< "2917","cryoglobulinemia","mesh","D003449"
< "2917","cryoglobulinemia","umls","C0010403"
< "2917","cryoglobulinemia","mondo","0005576"
---
> "3382","liposarcoma","mesh","D008080"
> "3382","liposarcoma","umls","C0023827"
> "3382","liposarcoma","mondo","0005060"
> "0111390","mucopolysaccharidosis Ih","umls","C0086795"
> "13356","senile ectropion","icd9cm","374.11"
> "13356","senile ectropion","umls","C0155193"
> "13356","senile ectropion","mondo","0001695"
> "11543","corneal abscess","icd10cm","H16.31"
> "11543","corneal abscess","icd9cm","370.55"
> "11543","corneal abscess","umls","C0155091"
> "11543","corneal abscess","mondo","0001307"
> "0070290","primary autosomal recessive microcephaly 6","mondo","0012029"
> "11541","recurrent corneal erosion","icd10cm","H18.83"
> "11541","recurrent corneal erosion","icd9cm","371.42"
> "11541","recurrent corneal erosion","umls","C0155119"
> "11541","recurrent corneal erosion","mondo","0001306"
> "11547","corneal deposit","icd10cm","H18.00"
> "11547","corneal deposit","icd9cm","371.10"
> "11547","corneal deposit","umls","C0162281"
> "11547","corneal deposit","mondo","0001308"
42,101c25,28
< "0070073","autosomal dominant non-syndromic intellectual disability 43","mondo","0014858"
< "4028","angioma serpiginosum","icd10cm","L81.7"
< "4028","angioma serpiginosum","mesh","C536366"
< "4028","angioma serpiginosum","umls","C0263637"
< "4028","angioma serpiginosum","mondo","0019803"
< "4029","gastritis","icd10cm","K29.7"
< "4029","gastritis","mesh","D005756"
< "4029","gastritis","umls","C0017152"
< "4029","gastritis","mondo","0004966"
< "6132","bronchitis","icd10cm","J20"
< "6132","bronchitis","icd10cm","J20.9"
< "6132","bronchitis","icd10cm","J40"
< "6132","bronchitis","icd10cm","J42"
< "6132","bronchitis","icd9cm","466.0"
< "6132","bronchitis","icd9cm","490"
< "6132","bronchitis","icd9cm","491"
< "6132","bronchitis","icd9cm","491.9"
< "6132","bronchitis","mesh","D001991"
< "6132","bronchitis","mesh","D029481"
< "6132","bronchitis","umls","C0006277"
< "6132","bronchitis","umls","C0008677"
< "6132","bronchitis","umls","C0149514"
< "6132","bronchitis","mondo","0003781"
< "0110434","dilated cardiomyopathy 1Z","icd10cm","I42.0"
< "0110434","dilated cardiomyopathy 1Z","mondo","0012745"
< "0070072","autosomal dominant non-syndromic intellectual disability 42","mondo","0014855"
< "11385","expressive language disorder","icd10cm","F80.1"
< "11385","expressive language disorder","icd9cm","315.31"
< "11385","expressive language disorder","umls","C0236826"
< "11385","expressive language disorder","mondo","0001276"
< "0110435","dilated cardiomyopathy 1GG","icd10cm","I42.0"
< "0110435","dilated cardiomyopathy 1GG","mondo","0013339"
< "10892","hypospadias","icd10cm","Q54"
< "10892","hypospadias","icd10cm","Q54.9"
< "10892","hypospadias","mesh","D007021"
< "10892","hypospadias","umls","C0848558"
< "10892","hypospadias","mondo","0005345"
< "0110340","osteogenesis imperfecta type 4","icd10cm","Q78.0"
< "0110340","osteogenesis imperfecta type 4","mondo","0008148"
< "14292","vulvar dystrophy","icd10cm","N90.4"
< "14292","vulvar dystrophy","icd9cm","624.0"
< "14292","vulvar dystrophy","umls","C0013426"
< "14292","vulvar dystrophy","mondo","0001938"
< "0050431","arrhythmogenic right ventricular cardiomyopathy","mesh","D019571"
< "0050431","arrhythmogenic right ventricular cardiomyopathy","umls","C0349788"
< "0050431","arrhythmogenic right ventricular cardiomyopathy","mondo","0016587"
< "3999","Bartholin's gland carcinoma","umls","C0349561"
< "3999","Bartholin's gland carcinoma","mondo","0002829"
< "3998","Bartholin's gland transitional cell carcinoma","umls","C1511053"
< "3998","Bartholin's gland transitional cell carcinoma","mondo","0002828"
< "0110346","osteogenesis imperfecta type 10","icd10cm","Q78.0"
< "0110346","osteogenesis imperfecta type 10","mondo","0013459"
< "7519","endocervical carcinoma","umls","C1299237"
< "7519","endocervical carcinoma","mondo","0004259"
< "0110431","dilated cardiomyopathy 1I","icd10cm","I42.0"
< "0110431","dilated cardiomyopathy 1I","mondo","0011482"
< "4930","nasal cavity adenocarcinoma","umls","C1334920"
< "4930","nasal cavity adenocarcinoma","mondo","0003211"
< "0060911","karyomegalic interstitial nephritis","icd10cm","N11.8"
< "0060911","karyomegalic interstitial nephritis","mondo","0013898"
---
> "5982","kidney fibrosarcoma","umls","C0238208"
> "5982","kidney fibrosarcoma","mondo","0003720"
> "5983","kidney osteogenic sarcoma","umls","C1335747"
> "5983","kidney osteogenic sarcoma","mondo","0003721"
103,118d29
< "4931","nasal cavity carcinoma","umls","C1377785"
< "4931","nasal cavity carcinoma","mondo","0003212"
< "0110433","dilated cardiomyopathy 1E","icd10cm","I42.0"
< "0110433","dilated cardiomyopathy 1E","mondo","0011003"
< "0090116","spondylocarpotarsal synostosis syndrome","icd10cm","Q76.4"
< "0090116","spondylocarpotarsal synostosis syndrome","mondo","0010094"
< "12700","hyperprolactinemia","icd10cm","E22.1"
< "12700","hyperprolactinemia","mesh","D002640"
< "12700","hyperprolactinemia","mesh","D006966"
< "12700","hyperprolactinemia","umls","C0008043"
< "12700","hyperprolactinemia","umls","C0020514"
< "12700","hyperprolactinemia","mondo","0024305"
< "4933","apocrine adenocarcinoma","umls","C0334346"
< "4933","apocrine adenocarcinoma","mondo","0003214"
< "2132","brain sarcoma","umls","C1332607"
< "2132","brain sarcoma","mondo","0002216"
122a34,37
> "0090093","hypogonadotropic hypogonadism 21 with or without anosmia","icd10cm","E23.0"
> "0090093","hypogonadotropic hypogonadism 21 with or without anosmia","mondo","0014107"
> "0090092","hypogonadotropic hypogonadism 3 with or without anosmia","icd10cm","E23.0"
> "0090092","hypogonadotropic hypogonadism 3 with or without anosmia","mondo","0009482"
127,135c42,43
< "10967","spastic hemiplegia","icd9cm","343.1"
< "10967","spastic hemiplegia","umls","C0270805"
< "10967","spastic hemiplegia","mondo","0001168"
< "10965","spastic diplegia","icd10cm","G80.1"
< "10965","spastic diplegia","icd9cm","343.0"
< "10965","spastic diplegia","mesh","D002547"
< "10965","spastic diplegia","umls","C0023882"
< "10965","spastic diplegia","umls","C0154695"
< "10965","spastic diplegia","mondo","0001167"
---
> "0110959","Gaucher's disease type III","icd10cm","E75.2"
> "0110959","Gaucher's disease type III","mondo","0009267"
141,143c49
< "2316","brain ischemia","mesh","D002545"
< "2316","brain ischemia","umls","C0007786"
< "2316","brain ischemia","mondo","0005299"
---
> "0110953","Waardenburg syndrome type 4A","mondo","0010192"
145,148c51
< "2314","malt worker's lung","icd10cm","J67.4"
< "2314","malt worker's lung","icd9cm","495.4"
< "2314","malt worker's lung","umls","C0155888"
< "2314","malt worker's lung","mondo","0002266"
---
> "0110951","Waardenburg syndrome type 2C","mondo","0011697"
154,180c57,63
< "10968","spastic monoplegia","icd9cm","343.3"
< "10968","spastic monoplegia","mesh","D002547"
< "10968","spastic monoplegia","umls","C0154698"
< "10968","spastic monoplegia","mondo","0001169"
< "0110867","congenital stationary night blindness 1C","mondo","0013183"
< "4939","ureter carcinoma","umls","C0600079"
< "4939","ureter carcinoma","mondo","0006481"
< "295","eye carcinoma","umls","C0848866"
< "295","eye carcinoma","mondo","0002466"
< "0110865","congenital stationary night blindness 1B","mondo","0009758"
< "0110932","nemaline myopathy 4","mondo","0012240"
< "1781","thyroid cancer","kegg","05216"
< "1781","thyroid cancer","icd10cm","C73"
< "1781","thyroid cancer","icd9cm","193"
< "1781","thyroid cancer","mesh","D013964"
< "1781","thyroid cancer","umls","C0007115"
< "1781","thyroid cancer","umls","C0040136"
< "1781","thyroid cancer","mondo","0002108"
< "0110864","congenital stationary night blindness 1F","mondo","0014026"
< "0090118","congenital amegakaryocytic thrombocytopenia","mesh","C535982"
< "0090118","congenital amegakaryocytic thrombocytopenia","umls","C1327915"
< "0090118","congenital amegakaryocytic thrombocytopenia","mondo","0011469"
< "6581","breast apocrine carcinoma","umls","C1332316"
< "6581","breast apocrine carcinoma","mondo","0003934"
< "0090119","ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","mesh","C535289"
< "0090119","ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","umls","C1785148"
< "0090119","ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","mondo","0007124"
---
> "0110954","Waardenburg syndrome type 4B","mondo","0013201"
> "2557","chondromalacia","icd10cm","M94.2"
> "2557","chondromalacia","icd10cm","M94.20"
> "2557","chondromalacia","icd9cm","733.92"
> "2557","chondromalacia","mesh","D002357"
> "2557","chondromalacia","umls","C0085700"
> "2557","chondromalacia","mondo","0002342"
183,184c66,67
< "0110831","Usher syndrome type 1D","icd10cm","H35.5"
< "0110831","Usher syndrome type 1D","mondo","0010984"
---
> "271","hemangioma of liver","umls","C0238246"
> "271","hemangioma of liver","mondo","0002404"
191,195c74,80
< "0110713","Oguchi disease-2","mondo","0013259"
< "0060829","Brooks-Wisniewski-Brown syndrome","icd10cm","Q87.8"
< "0060829","Brooks-Wisniewski-Brown syndrome","mondo","0010376"
< "0110837","Usher syndrome type 1K","icd10cm","H35.5"
< "0110837","Usher syndrome type 1K","mondo","0014001"
---
> "275","gastric hemangioma","umls","C1333770"
> "275","gastric hemangioma","mondo","0002414"
> "0110836","Usher syndrome type 1J","icd10cm","H35.5"
> "0110836","Usher syndrome type 1J","mondo","0013935"
> "277","chorioangioma","mesh","D006391"
> "277","chorioangioma","umls","C0677608"
> "277","chorioangioma","mondo","0006375"
198,199c83,84
< "0050740","Qazi Markouizos syndrome","mesh","C536259"
< "0050740","Qazi Markouizos syndrome","mondo","0010816"
---
> "0060826","syndromic X-linked intellectual disability Shashi type","icd10cm","Q87.8"
> "0060826","syndromic X-linked intellectual disability Shashi type","mondo","0010277"
204c89,90
< "0110712","Oguchi disease-1","mondo","0009775"
---
> "0060824","syndromic X-linked intellectual disability Raymond type","icd10cm","Q87.8"
> "0060824","syndromic X-linked intellectual disability Raymond type","mondo","0010427"
209,214c95,97
< "0050747","lymphoplasmacytic lymphoma","icd10cm","C88.0"
< "0050747","lymphoplasmacytic lymphoma","icd9cm","273.3"
< "0050747","lymphoplasmacytic lymphoma","mesh","D008258"
< "0050747","lymphoplasmacytic lymphoma","umls","C0024419"
< "0050747","lymphoplasmacytic lymphoma","umls","C2936755"
< "0050747","lymphoplasmacytic lymphoma","mondo","0000432"
---
> "0060821","syndromic X-linked intellectual disability 14","mesh","C537724"
> "0060821","syndromic X-linked intellectual disability 14","umls","C0796022"
> "0060821","syndromic X-linked intellectual disability 14","mondo","0010398"
217,226c100,109
< "827","ureter tuberculosis","icd9cm","016.2"
< "827","ureter tuberculosis","umls","C0152800"
< "827","ureter tuberculosis","mondo","0004517"
< "5099","middle ear cancer","umls","C0345617"
< "5099","middle ear cancer","mondo","0003275"
< "0111059","Bernard-Soulier syndrome type A2","mondo","0007930"
< "0111058","platelet-type bleeding disorder 12","mondo","0011588"
< "0060881","renal hypomagnesemia 5 with ocular involvement","mesh","C536148"
< "0060881","renal hypomagnesemia 5 with ocular involvement","umls","C2931121"
< "0060881","renal hypomagnesemia 5 with ocular involvement","mondo","0009548"
---
> "12016","frontal lobe neoplasm","icd10cm","C71.1"
> "12016","frontal lobe neoplasm","icd9cm","191.1"
> "12016","frontal lobe neoplasm","umls","C0153635"
> "12016","frontal lobe neoplasm","umls","C1263886"
> "12016","frontal lobe neoplasm","mondo","0001421"
> "12010","anterior ischemic optic neuropathy","icd10cm","H47.01"
> "12010","anterior ischemic optic neuropathy","icd9cm","377.41"
> "12010","anterior ischemic optic neuropathy","mesh","D018917"
> "12010","anterior ischemic optic neuropathy","umls","C0155305"
> "12010","anterior ischemic optic neuropathy","mondo","0006649"
229,247d111
< "0111051","platelet-type bleeding disorder 18","icd10cm","D69.1"
< "0111051","platelet-type bleeding disorder 18","mondo","0014386"
< "0111050","Quebec platelet disorder","mesh","C536260"
< "0111050","Quebec platelet disorder","umls","C1866423"
< "0111050","Quebec platelet disorder","mondo","0011136"
< "0111053","platelet-type bleeding disorder 15","mondo","0014078"
< "0111052","Scott syndrome","mesh","C563120"
< "0111052","Scott syndrome","umls","C0796149"
< "0111052","Scott syndrome","mondo","0009885"
< "0111055","platelet-type bleeding disorder 20","mondo","0014830"
< "0111054","von Willebrand's disease 3","mesh","D056729"
< "0111054","von Willebrand's disease 3","umls","C1264041"
< "0111054","von Willebrand's disease 3","mondo","0010191"
< "0111057","platelet-type bleeding disorder 11","icd10cm","D69.8"
< "0111057","platelet-type bleeding disorder 11","mondo","0013623"
< "0111056","platelet-type bleeding disorder 3","icd10cm","D69.8"
< "0111056","platelet-type bleeding disorder 3","mondo","0008332"
< "2441","frontal sinus squamous cell carcinoma","umls","C1333646"
< "2441","frontal sinus squamous cell carcinoma","mondo","0002301"
251,254c115
< "0050120","hemophagocytic lymphohistiocytosis","icd10cm","D76.1"
< "0050120","hemophagocytic lymphohistiocytosis","mesh","D051359"
< "0050120","hemophagocytic lymphohistiocytosis","umls","C0024291"
< "0050120","hemophagocytic lymphohistiocytosis","mondo","0015540"
---
> "0070298","multiple epiphyseal dysplasia 2","mondo","0010844"
260c121,124
< "0070295","primary autosomal dominant microcephaly 18","mondo","0054593"
---
> "9256","colorectal cancer","kegg","05210"
> "9256","colorectal cancer","mesh","D015179"
> "9256","colorectal cancer","umls","C1527249"
> "9256","colorectal cancer","mondo","0005575"
262c126,134
< "0070296","primary autosomal recessive microcephaly","mondo","0016660"
---
> "9254","mast-cell leukemia","icd10cm","C94.3"
> "9254","mast-cell leukemia","icd10cm","C94.30"
> "9254","mast-cell leukemia","mesh","D007946"
> "9254","mast-cell leukemia","umls","C0023461"
> "9254","mast-cell leukemia","mondo","0020334"
> "9255","frontotemporal dementia","mesh","C563003"
> "9255","frontotemporal dementia","mesh","D057180"
> "9255","frontotemporal dementia","umls","C0520716"
> "9255","frontotemporal dementia","mondo","0017276"
269,272c141,145
< "0070290","primary autosomal recessive microcephaly 6","mondo","0012029"
< "9250","acrocallosal syndrome","mesh","D055673"
< "9250","acrocallosal syndrome","umls","C0796147"
< "9250","acrocallosal syndrome","mondo","0008708"
---
> "9253","gastrointestinal stromal tumor","icd10cm","C49.A"
> "9253","gastrointestinal stromal tumor","mesh","D046152"
> "9253","gastrointestinal stromal tumor","umls","C0238198"
> "9253","gastrointestinal stromal tumor","mondo","0011719"
> "0070293","primary autosomal recessive microcephaly 2 with or without cortical malformations","mondo","0011435"
274,371c147,151
< "0080332","bicuspid aortic valve disease","mondo","0007194"
< "0060285","parietal foramina","mesh","C566826"
< "0060285","parietal foramina","umls","C1868598"
< "0060285","parietal foramina","mondo","0018953"
< "0070059","autosomal dominant non-syndromic intellectual disability 29","mondo","0014482"
< "0070058","Helsmoortel-Van Der Aa Syndrome","mondo","0014379"
< "0070057","autosomal dominant non-syndromic intellectual disability 27","mondo","0014376"
< "0070056","autosomal dominant non-syndromic intellectual disability 26","mondo","0014361"
< "0070055","Xia-Gibbs Syndrome","mondo","0014358"
< "0070054","autosomal dominant non-syndromic intellectual disability 24","mondo","0014357"
< "106","pleural tuberculosis","icd10cm","A15.6"
< "106","pleural tuberculosis","icd9cm","010.1"
< "106","pleural tuberculosis","icd9cm","012.0"
< "106","pleural tuberculosis","icd9cm","012.00"
< "106","pleural tuberculosis","mesh","D014396"
< "106","pleural tuberculosis","umls","C0041326"
< "106","pleural tuberculosis","umls","C0152531"
< "106","pleural tuberculosis","mondo","0005922"
< "0070052","autosomal dominant non-syndromic intellectual disability 22","mondo","0012869"
< "0070051","autosomal dominant non-syndromic intellectual disability 21","mondo","0014213"
< "0070050","autosomal dominant mental retardation 20","mondo","0013266"
< "4813","adult brain stem glioma","umls","C0278873"
< "4813","adult brain stem glioma","mondo","0003153"
< "2047","hepatitis D","mesh","D003699"
< "2047","hepatitis D","umls","C0011226"
< "2047","hepatitis D","mondo","0005789"
< "0110639","congenital muscular dystrophy due to integrin alpha-7 deficiency","icd10cm","G71.2"
< "0110639","congenital muscular dystrophy due to integrin alpha-7 deficiency","mondo","0013177"
< "2043","hepatitis B","mesh","D006509"
< "2043","hepatitis B","umls","C0019163"
< "2043","hepatitis B","mondo","0005344"
< "0110632","megaconial type congenital muscular dystrophy","icd10cm","G71.2"
< "0110632","megaconial type congenital muscular dystrophy","mondo","0011246"
< "0110633","rigid spine muscular dystrophy 1","icd10cm","G71.2"
< "0110633","rigid spine muscular dystrophy 1","icd10cm","G71.8"
< "0110633","rigid spine muscular dystrophy 1","mesh","C535683"
< "0110633","rigid spine muscular dystrophy 1","mondo","0011271"
< "0110630","Wolfram syndrome 2","icd10cm","E13.8"
< "0110630","Wolfram syndrome 2","mondo","0011502"
< "12522","bagassosis","icd10cm","J67.1"
< "12522","bagassosis","icd9cm","495.1"
< "12522","bagassosis","mesh","D011009"
< "12522","bagassosis","umls","C0004681"
< "12522","bagassosis","mondo","0001540"
< "0110636","congenital merosin-deficient muscular dystrophy 1A","mesh","C537384"
< "0110636","congenital merosin-deficient muscular dystrophy 1A","umls","C1263858"
< "0110636","congenital merosin-deficient muscular dystrophy 1A","mondo","0011925"
< "0110637","muscular dystrophy-dystroglycanopathy type B6","icd10cm","G71.2"
< "0110637","muscular dystrophy-dystroglycanopathy type B6","mondo","0012138"
< "0110634","congenital muscular dystrophy 1B","icd10cm","G71.2"
< "0110634","congenital muscular dystrophy 1B","mondo","0011486"
< "0110635","muscular dystrophy-dystroglycanopathy type B5","icd10cm","G71.2"
< "0110635","muscular dystrophy-dystroglycanopathy type B5","mondo","0011688"
< "12129","bulimia nervosa","icd10cm","F50.2"
< "12129","bulimia nervosa","mesh","D002032"
< "12129","bulimia nervosa","mesh","D052018"
< "12129","bulimia nervosa","umls","C0006370"
< "12129","bulimia nervosa","mondo","0005452"
< "11612","polycystic ovary syndrome","icd10cm","E28.2"
< "11612","polycystic ovary syndrome","icd9cm","256.4"
< "11612","polycystic ovary syndrome","mesh","D011085"
< "11612","polycystic ovary syndrome","umls","C0032460"
< "11612","polycystic ovary syndrome","mondo","0008487"
< "9415","allergic asthma","icd10cm","J45"
< "9415","allergic asthma","icd9cm","493.0"
< "9415","allergic asthma","umls","C0155877"
< "9415","allergic asthma","mondo","0004784"
< "11262","ornithosis","icd10cm","A70"
< "11262","ornithosis","icd9cm","073"
< "11262","ornithosis","icd9cm","073.9"
< "11262","ornithosis","mesh","D009956"
< "11262","ornithosis","umls","C0029291"
< "11262","ornithosis","mondo","0005888"
< "0111140","IGSF1 deficiency syndrome","icd10cm","E03.1"
< "0111140","IGSF1 deficiency syndrome","mondo","0010475"
< "8302","mixed endometrial stromal and smooth muscle tumor","umls","C1513364"
< "8302","mixed endometrial stromal and smooth muscle tumor","mondo","0004526"
< "10632","Wolfram syndrome","mesh","D014929"
< "10632","Wolfram syndrome","umls","C0043207"
< "10632","Wolfram syndrome","mondo","0018105"
< "820","myocarditis","kegg","05416"
< "820","myocarditis","icd10cm","I51.4"
< "820","myocarditis","icd9cm","429.0"
< "820","myocarditis","mesh","D009205"
< "820","myocarditis","umls","C0027059"
< "820","myocarditis","mondo","0004496"
< "10149","long bones of lower limb cancer","icd10cm","C40.2"
< "10149","long bones of lower limb cancer","icd9cm","170.7"
< "10149","long bones of lower limb cancer","umls","C0153517"
< "10149","long bones of lower limb cancer","mondo","0000952"
< "14133","Masters-Allen syndrome","icd9cm","620.6"
< "14133","Masters-Allen syndrome","umls","C0152079"
< "14133","Masters-Allen syndrome","mondo","0001887"
< "176","cardiovascular cancer","umls","C0497243"
< "176","cardiovascular cancer","mondo","0002100"
< "4140","biliary dyskinesia","mesh","D001657"
< "4140","biliary dyskinesia","umls","C0005416"
< "4140","biliary dyskinesia","mondo","0005667"
---
> "10892","hypospadias","icd10cm","Q54"
> "10892","hypospadias","icd10cm","Q54.9"
> "10892","hypospadias","mesh","D007021"
> "10892","hypospadias","umls","C0848558"
> "10892","hypospadias","mondo","0005345"
376,379c156,160
< "0110494","autosomal recessive nonsyndromic deafness 36","icd10cm","H90.3"
< "0110494","autosomal recessive nonsyndromic deafness 36","mondo","0012170"
< "0110495","autosomal recessive nonsyndromic deafness 37","icd10cm","H90.3"
< "0110495","autosomal recessive nonsyndromic deafness 37","mondo","0011912"
---
> "0050633","ocular albinism","mesh","D016117"
> "0050633","ocular albinism","mondo","0017304"
> "0050632","oculocutaneous albinism","icd10cm","E70.3"
> "0050632","oculocutaneous albinism","mesh","D016115"
> "0050632","oculocutaneous albinism","mondo","0018910"
383,388c164,166
< "0110493","autosomal recessive nonsyndromic deafness 35","icd10cm","H90.3"
< "0110493","autosomal recessive nonsyndromic deafness 35","mondo","0012060"
< "0110490","autosomal recessive nonsyndromic deafness 31","icd10cm","H90.3"
< "0110490","autosomal recessive nonsyndromic deafness 31","mondo","0011767"
< "0110491","autosomal recessive nonsyndromic deafness 32","icd10cm","H90.3"
< "0110491","autosomal recessive nonsyndromic deafness 32","mondo","0012091"
---
> "0050634","alopecia universalis","mondo","0008757"
> "0050637","Finnish type amyloidosis","mondo","0007097"
> "0050636","familial visceral amyloidosis","mondo","0007099"
391,424c169,181
< "0110906","inflammatory bowel disease 21","mondo","0012875"
< "0110498","autosomal recessive nonsyndromic deafness 4","icd10cm","H90.3"
< "0110498","autosomal recessive nonsyndromic deafness 4","mondo","0010933"
< "0110499","autosomal recessive nonsyndromic deafness 40","icd10cm","H90.3"
< "0110499","autosomal recessive nonsyndromic deafness 40","mondo","0012002"
< "0110126","Bardet-Biedl syndrome 4","icd10cm","Q87.89"
< "0110126","Bardet-Biedl syndrome 4","mondo","0014433"
< "0110127","Bardet-Biedl syndrome 5","icd10cm","Q87.89"
< "0110127","Bardet-Biedl syndrome 5","mondo","0014434"
< "0110124","Bardet-Biedl syndrome 2","icd10cm","Q87.89"
< "0110124","Bardet-Biedl syndrome 2","mondo","0014432"
< "0110125","Bardet-Biedl syndrome 3","icd10cm","Q87.89"
< "0110125","Bardet-Biedl syndrome 3","mondo","0010832"
< "0110122","Axenfeld-Rieger syndrome type 3","icd10cm","Q13.8"
< "0110122","Axenfeld-Rieger syndrome type 3","mondo","0011233"
< "0110123","Bardet-Biedl syndrome 1","icd10cm","Q87.89"
< "0110123","Bardet-Biedl syndrome 1","mondo","0008854"
< "0110120","Axenfeld-Rieger syndrome type 1","icd10cm","Q13.8"
< "0110120","Axenfeld-Rieger syndrome type 1","mondo","0008386"
< "0110121","Axenfeld-Rieger syndrome type 2","icd10cm","Q13.8"
< "0110121","Axenfeld-Rieger syndrome type 2","mondo","0011097"
< "5299","endometrial clear cell adenocarcinoma","umls","C0279765"
< "5299","endometrial clear cell adenocarcinoma","mondo","0006191"
< "0110128","Bardet-Biedl syndrome 6","icd10cm","Q87.89"
< "0110128","Bardet-Biedl syndrome 6","mondo","0011523"
< "0110129","Bardet-Biedl syndrome 7","icd10cm","Q87.89"
< "0110129","Bardet-Biedl syndrome 7","mondo","0014435"
< "12236","primary biliary cirrhosis","icd10cm","K74.3"
< "12236","primary biliary cirrhosis","icd10cm","K74.5"
< "12236","primary biliary cirrhosis","icd9cm","571.6"
< "12236","primary biliary cirrhosis","mesh","D008105"
< "12236","primary biliary cirrhosis","umls","C0008312"
< "12236","primary biliary cirrhosis","umls","C0023892"
< "12236","primary biliary cirrhosis","mondo","0005388"
---
> "1936","atherosclerosis","icd10cm","I25.1"
> "1936","atherosclerosis","icd10cm","I70"
> "1936","atherosclerosis","icd9cm","440"
> "1936","atherosclerosis","mesh","D050197"
> "1936","atherosclerosis","umls","C0004153"
> "1936","atherosclerosis","mondo","0005311"
> "3512","neurofibrosarcoma","mesh","D018319"
> "3512","neurofibrosarcoma","umls","C0206729"
> "3512","neurofibrosarcoma","mondo","0002675"
> "3517","conventional fibrosarcoma","umls","C1333156"
> "3517","conventional fibrosarcoma","mondo","0002677"
> "3516","adult fibrosarcoma","umls","C0278595"
> "3516","adult fibrosarcoma","mondo","0002676"
429a187,188
> "2685","ossifying fibromyxoid tumor","umls","C1266128"
> "2685","ossifying fibromyxoid tumor","mondo","0006330"
432,433c191,192
< "6209","malignant mediastinum hemangiopericytoma","umls","C1334598"
< "6209","malignant mediastinum hemangiopericytoma","mondo","0003809"
---
> "2682","intracystic papillary adenoma","umls","C0334374"
> "2682","intracystic papillary adenoma","mondo","0002388"
437,438c196,199
< "7511","breast intraductal papillomatosis","umls","C1334247"
< "7511","breast intraductal papillomatosis","mondo","0004253"
---
> "14686","Axenfeld-Rieger syndrome","icd10cm","Q13.81"
> "14686","Axenfeld-Rieger syndrome","mesh","C535679"
> "14686","Axenfeld-Rieger syndrome","umls","C0265341"
> "14686","Axenfeld-Rieger syndrome","mondo","0019187"
444,445c205,206
< "6804","colon Kaposi sarcoma","umls","C1333091"
< "6804","colon Kaposi sarcoma","mondo","0003997"
---
> "0110304","autosomal dominant limb-girdle muscular dystrophy type 2","icd10cm","G71.0"
> "0110304","autosomal dominant limb-girdle muscular dystrophy type 2","mondo","0012034"
450,479c211,219
< "5293","extrahepatic bile duct leiomyosarcoma","umls","C1333508"
< "5293","extrahepatic bile duct leiomyosarcoma","mondo","0003377"
< "9744","type 1 diabetes mellitus","kegg","04940"
< "9744","type 1 diabetes mellitus","icd10cm","E10"
< "9744","type 1 diabetes mellitus","mesh","D003922"
< "9744","type 1 diabetes mellitus","umls","C0011854"
< "9744","type 1 diabetes mellitus","mondo","0005147"
< "0050430","multiple endocrine neoplasia type 2A","icd10cm","E31.22"
< "0050430","multiple endocrine neoplasia type 2A","icd9cm","258.02"
< "0050430","multiple endocrine neoplasia type 2A","mesh","D018813"
< "0050430","multiple endocrine neoplasia type 2A","umls","C0025268"
< "0050430","multiple endocrine neoplasia type 2A","mondo","0008234"
< "10567","late yaws","icd10cm","A66.1"
< "10567","late yaws","icd10cm","A66.4"
< "10567","late yaws","icd9cm","102.1"
< "10567","late yaws","icd9cm","102.4"
< "10567","late yaws","umls","C0153234"
< "10567","late yaws","umls","C0276007"
< "10567","late yaws","umls","C1517744"
< "10567","late yaws","mondo","0001066"
< "0050886","Troyer syndrome","icd10cm","G11.4"
< "0050886","Troyer syndrome","mondo","0010156"
< "10568","early yaws","icd10cm","A66.0"
< "10568","early yaws","icd10cm","A66.6"
< "10568","early yaws","icd9cm","102.0"
< "10568","early yaws","icd9cm","102.6"
< "10568","early yaws","umls","C0275990"
< "10568","early yaws","umls","C0275998"
< "10568","early yaws","umls","C0343834"
< "10568","early yaws","mondo","0001067"
---
> "90","degenerative disc disease","umls","C0410606"
> "90","degenerative disc disease","mondo","0011385"
> "93","language disorder","icd10cm","F80.9"
> "93","language disorder","mesh","D007806"
> "93","language disorder","umls","C0023015"
> "93","language disorder","mondo","0004750"
> "92","speech disorder","mesh","D013064"
> "92","speech disorder","umls","C0037822"
> "92","speech disorder","mondo","0004730"
485,688c225,255
< "0070277","primary autosomal recessive microcephaly 15","mondo","0014660"
< "0070276","hereditary nonpolyposis colorectal cancer type 7","mondo","0013725"
< "1993","rectum cancer","icd10cm","C20"
< "1993","rectum cancer","icd9cm","154.1"
< "1993","rectum cancer","mesh","D012004"
< "1993","rectum cancer","umls","C0007113"
< "1993","rectum cancer","umls","C0949022"
< "1993","rectum cancer","mondo","0006519"
< "0070274","hereditary nonpolyposis colorectal cancer type 2","mondo","0012249"
< "1995","rectum sarcoma","umls","C1335688"
< "1995","rectum sarcoma","mondo","0002168"
< "0070272","hereditary nonpolyposis colorectal cancer type 5","mondo","0013710"
< "1625","breast adenoma","umls","C1328385"
< "1625","breast adenoma","mondo","0002058"
< "0070270","hereditary nonpolyposis colorectal cancer type 8","mondo","0013196"
< "1999","chronic eustachian salpingitis","icd10cm","H68.02"
< "1999","chronic eustachian salpingitis","icd10cm","H68.029"
< "1999","chronic eustachian salpingitis","icd9cm","381.52"
< "1999","chronic eustachian salpingitis","umls","C0155430"
< "1999","chronic eustachian salpingitis","mondo","0002170"
< "8850","salivary gland cancer","icd10cm","C08"
< "8850","salivary gland cancer","icd9cm","142.8"
< "8850","salivary gland cancer","umls","C0153362"
< "8850","salivary gland cancer","mondo","0004669"
< "0070279","primary autosomal recessive microcephaly 14","mondo","0014623"
< "0070278","primary autosomal recessive microcephaly 7","mondo","0012989"
< "0110012","advanced sleep phase syndrome 2","mondo","0014088"
< "0110545","autosomal dominant nonsyndromic deafness 13","icd10cm","H90.3"
< "0110545","autosomal dominant nonsyndromic deafness 13","mondo","0011159"
< "0110010","achromatopsia 4","mondo","0013465"
< "0110011","advanced sleep phase syndrome 1","mondo","0011442"
< "0110540","autosomal recessive nonsyndromic deafness 98","icd10cm","H90.3"
< "0110540","autosomal recessive nonsyndromic deafness 98","mondo","0013929"
< "0110541","autosomal dominant nonsyndromic deafness 1","icd10cm","H90.3"
< "0110541","autosomal dominant nonsyndromic deafness 1","mondo","0007424"
< "0110542","autosomal dominant nonsyndromic deafness 10","icd10cm","H90.3"
< "0110542","autosomal dominant nonsyndromic deafness 10","mondo","0011031"
< "0110015","age related macular degeneration 2","mondo","0007932"
< "0110018","age related macular degeneration 6","mondo","0013406"
< "0110019","age related macular degeneration 7","mondo","0012419"
< "0110548","autosomal dominant nonsyndromic deafness 17","icd10cm","H90.3"
< "0110548","autosomal dominant nonsyndromic deafness 17","mondo","0011350"
< "0110549","autosomal dominant nonsyndromic deafness 18","icd10cm","H90.3"
< "0110549","autosomal dominant nonsyndromic deafness 18","mondo","0011625"
< "5677","extragonadal nonseminomatous germ cell tumor","umls","C1334582"
< "5677","extragonadal nonseminomatous germ cell tumor","mondo","0003578"
< "2862","glucosephosphate dehydrogenase deficiency","mesh","D005955"
< "2862","glucosephosphate dehydrogenase deficiency","umls","C2939465"
< "2862","glucosephosphate dehydrogenase deficiency","mondo","0005775"
< "7147","ankylosing spondylitis","icd10cm","M45"
< "7147","ankylosing spondylitis","icd9cm","720.0"
< "7147","ankylosing spondylitis","mesh","D013167"
< "7147","ankylosing spondylitis","umls","C0038013"
< "7147","ankylosing spondylitis","mondo","0005306"
< "3016","breast malignant phyllodes tumor","mesh","D003557"
< "3016","breast malignant phyllodes tumor","umls","C0238031"
< "3016","breast malignant phyllodes tumor","umls","C0346154"
< "3016","breast malignant phyllodes tumor","umls","C0600066"
< "3016","breast malignant phyllodes tumor","mondo","0002489"
< "557","kidney disease","icd10cm","N08"
< "557","kidney disease","icd10cm","N28.9"
< "557","kidney disease","mesh","D007674"
< "557","kidney disease","umls","C0022658"
< "557","kidney disease","mondo","0005240"
< "551","toxic pneumonitis","icd9cm","506.9"
< "551","toxic pneumonitis","umls","C0041881"
< "551","toxic pneumonitis","mondo","0003479"
< "552","pneumonia","mesh","D011014"
< "552","pneumonia","umls","C0032285"
< "552","pneumonia","mondo","0005249"
< "14247","chronic purulent otitis media","icd10cm","H66.3"
< "14247","chronic purulent otitis media","icd9cm","382.3"
< "14247","chronic purulent otitis media","umls","C0271454"
< "14247","chronic purulent otitis media","mondo","0001920"
< "0080163","otulipenia","mondo","0014912"
< "14243","chronic perichondritis of pinna","icd9cm","380.02"
< "14243","chronic perichondritis of pinna","umls","C0155391"
< "14243","chronic perichondritis of pinna","mondo","0001917"
< "14717","centronuclear myopathy","mesh","D020914"
< "14717","centronuclear myopathy","umls","C0175709"
< "14717","centronuclear myopathy","mondo","0018947"
< "5408","Paget's disease of bone","icd10cm","M88"
< "5408","Paget's disease of bone","mesh","D010001"
< "5408","Paget's disease of bone","umls","C0029401"
< "5408","Paget's disease of bone","mondo","0005382"
< "14248","chronic atticoantral disease","icd10cm","H66.2"
< "14248","chronic atticoantral disease","icd10cm","H66.20"
< "14248","chronic atticoantral disease","icd9cm","382.2"
< "14248","chronic atticoantral disease","umls","C0155441"
< "14248","chronic atticoantral disease","mondo","0001921"
< "0060344","acrodermatitis chronica atrophicans","icd9cm","701.8"
< "0060344","acrodermatitis chronica atrophicans","umls","C0029805"
< "0060344","acrodermatitis chronica atrophicans","mondo","0006524"
< "0060341","agnathia-otocephaly complex","icd10cm","Q18.2"
< "0060341","agnathia-otocephaly complex","mesh","C562503"
< "0060341","agnathia-otocephaly complex","mondo","0008740"
< "3342","bone inflammation disease","mesh","D010000"
< "3342","bone inflammation disease","umls","C0029400"
< "3342","bone inflammation disease","mondo","0002614"
< "3343","glycoproteinosis","mesh","D009081"
< "3343","glycoproteinosis","umls","C0026697"
< "3343","glycoproteinosis","mondo","0009738"
< "1192","peripheral nervous system neoplasm","mesh","D010524"
< "1192","peripheral nervous system neoplasm","mesh","D018317"
< "1192","peripheral nervous system neoplasm","umls","C0031118"
< "1192","peripheral nervous system neoplasm","umls","C0206727"
< "1192","peripheral nervous system neoplasm","mondo","0001406"
< "3347","osteosarcoma","mesh","D012516"
< "3347","osteosarcoma","mesh","D018213"
< "3347","osteosarcoma","umls","C0029463"
< "3347","osteosarcoma","umls","C0206639"
< "3347","osteosarcoma","mondo","0009807"
< "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","mesh","C537157"
< "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","umls","C1855840"
< "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","mondo","0009426"
< "0060349","microcephaly with or without chorioretinopathy, lymphedema, or mental retardation","mesh","C537711"
< "0060349","microcephaly with or without chorioretinopathy, lymphedema, or mental retardation","umls","C1835265"
< "0060349","microcephaly with or without chorioretinopathy, lymphedema, or mental retardation","mondo","0007918"
< "0050655","Bamforth-Lazarus syndrome","mondo","0009437"
< "14392","thrombophlebitis migrans","icd10cm","I82.1"
< "14392","thrombophlebitis migrans","icd9cm","453.1"
< "14392","thrombophlebitis migrans","umls","C0152250"
< "14392","thrombophlebitis migrans","mondo","0001954"
< "1754","mitral valve stenosis","mesh","D008946"
< "1754","mitral valve stenosis","umls","C0026269"
< "1754","mitral valve stenosis","mondo","0005852"
< "1752","ocular melanoma","mondo","0006325"
< "4258","Weissenbacher-Zweymuller syndrome","icd10cm","Q87.0"
< "4258","Weissenbacher-Zweymuller syndrome","mesh","D010855"
< "4258","Weissenbacher-Zweymuller syndrome","umls","C0031900"
< "4258","Weissenbacher-Zweymuller syndrome","mondo","0010195"
< "4252","Alexander disease","mesh","D038261"
< "4252","Alexander disease","umls","C0270726"
< "4252","Alexander disease","mondo","0008752"
< "13945","CADASIL","mesh","D046589"
< "13945","CADASIL","umls","C0751587"
< "13945","CADASIL","mondo","0007432"
< "4257","Caffey disease","icd10cm","M89.8"
< "4257","Caffey disease","mesh","D006958"
< "4257","Caffey disease","umls","C0020497"
< "4257","Caffey disease","mondo","0007244"
< "5533","endometrial squamous cell carcinoma","umls","C1333396"
< "5533","endometrial squamous cell carcinoma","mondo","0006198"
< "0060377","orofaciodigital syndrome VII","mesh","C563104"
< "0060377","orofaciodigital syndrome VII","mondo","0012049"
< "5530","thymus squamous cell carcinoma","umls","C1336082"
< "5530","thymus squamous cell carcinoma","mondo","0003493"
< "5537","squamous cell bile duct carcinoma","umls","C0861861"
< "5537","squamous cell bile duct carcinoma","mondo","0003500"
< "0060854","autosomal recessive pseudohypoaldosteronism type 1","mesh","D011546"
< "0060854","autosomal recessive pseudohypoaldosteronism type 1","umls","C0268436"
< "0060854","autosomal recessive pseudohypoaldosteronism type 1","mondo","0009917"
< "5535","gallbladder squamous cell carcinoma","umls","C0279658"
< "5535","gallbladder squamous cell carcinoma","mondo","0006220"
< "5534","renal pelvis squamous cell carcinoma","umls","C0238409"
< "5534","renal pelvis squamous cell carcinoma","mondo","0003497"
< "5539","ureter squamous cell carcinoma","umls","C1336879"
< "5539","ureter squamous cell carcinoma","mondo","0003502"
< "11661","blue color blindness","icd10cm","H53.55"
< "11661","blue color blindness","icd9cm","368.53"
< "11661","blue color blindness","mesh","D003117"
< "11661","blue color blindness","umls","C0155017"
< "11661","blue color blindness","mondo","0008610"
< "0060123","connective tissue benign neoplasm","mesh","D012983"
< "0060123","connective tissue benign neoplasm","umls","C0037579"
< "0060123","connective tissue benign neoplasm","mondo","0000654"
< "1287","cardiovascular system disease","icd9cm","429.2"
< "1287","cardiovascular system disease","mesh","D002318"
< "1287","cardiovascular system disease","umls","C0007222"
< "1287","cardiovascular system disease","mondo","0004995"
< "11168","anogenital venereal wart","icd10cm","A63.0"
< "11168","anogenital venereal wart","icd9cm","078.11"
< "11168","anogenital venereal wart","mesh","D003218"
< "11168","anogenital venereal wart","umls","C0009663"
< "11168","anogenital venereal wart","umls","C0554632"
< "11168","anogenital venereal wart","mondo","0005647"
< "0060127","gamma heavy chain disease","mondo","0015046"
< "1283","enterocele","icd10cm","K46"
< "1283","enterocele","icd10cm","N81.5"
< "1283","enterocele","icd9cm","618.6"
< "1283","enterocele","mesh","D006547"
< "1283","enterocele","umls","C0205792"
< "1283","enterocele","mondo","0001589"
< "0050662","bestrophinopathy","mesh","C567518"
< "0050662","bestrophinopathy","mondo","0012733"
< "8725","vascular dementia","icd10cm","F01"
< "8725","vascular dementia","icd10cm","F01.5"
< "8725","vascular dementia","icd9cm","290.4"
< "8725","vascular dementia","mesh","D015140"
< "8725","vascular dementia","mesh","D015161"
< "8725","vascular dementia","umls","C0011263"
< "8725","vascular dementia","umls","C0011269"
< "8725","vascular dementia","mondo","0004648"
< "1289","neurodegenerative disease","icd10cm","G31.9"
< "1289","neurodegenerative disease","mesh","D019636"
< "1289","neurodegenerative disease","umls","C0524851"
< "1289","neurodegenerative disease","umls","C1285162"
< "1289","neurodegenerative disease","mondo","0005559"
< "0110469","autosomal recessive nonsyndromic deafness 14","icd10cm","H90.3"
< "0110469","autosomal recessive nonsyndromic deafness 14","mondo","0011360"
< "11162","respiratory failure","icd10cm","J96.0"
< "11162","respiratory failure","icd9cm","518.81"
< "11162","respiratory failure","umls","C0264490"
< "11162","respiratory failure","mondo","0021113"
---
> "11665","Patau syndrome","icd10cm","Q91.7"
> "11665","Patau syndrome","icd9cm","758.1"
> "11665","Patau syndrome","mesh","D000073839"
> "11665","Patau syndrome","umls","C0152095"
> "11665","Patau syndrome","mondo","0001333"
> "14681","Silver-Russell syndrome","icd10cm","Q87.1"
> "14681","Silver-Russell syndrome","mesh","D056730"
> "14681","Silver-Russell syndrome","umls","C0175693"
> "14681","Silver-Russell syndrome","mondo","0008394"
> "13050","corpus luteum cyst","icd9cm","620.1"
> "13050","corpus luteum cyst","umls","C0156361"
> "13050","corpus luteum cyst","mondo","0001625"
> "12836","senile entropion","icd9cm","374.01"
> "12836","senile entropion","umls","C0155188"
> "12836","senile entropion","mondo","0001591"
> "13912","acquired color blindness","icd10cm","H53.52"
> "13912","acquired color blindness","icd9cm","368.55"
> "13912","acquired color blindness","mesh","D003117"
> "13912","acquired color blindness","umls","C0155018"
> "13912","acquired color blindness","mondo","0001828"
> "1176","bronchial disease","mesh","D001982"
> "1176","bronchial disease","umls","C0006261"
> "1176","bronchial disease","mondo","0001358"
> "1172","hyperlipoproteinemia type IV","icd10cm","E78.1"
> "1172","hyperlipoproteinemia type IV","icd9cm","272.1"
> "1172","hyperlipoproteinemia type IV","mesh","D006953"
> "1172","hyperlipoproteinemia type IV","umls","C0020480"
> "1172","hyperlipoproteinemia type IV","mondo","0007761"
> "1171","hyperlipoproteinemia type V","mesh","D006954"
> "1171","hyperlipoproteinemia type V","umls","C0020481"
> "1171","hyperlipoproteinemia type V","mondo","0007762"
693,734c260,278
< "0001816","angiosarcoma","mesh","D006394"
< "0001816","angiosarcoma","umls","C0018923"
< "0001816","angiosarcoma","umls","C0854893"
< "0001816","angiosarcoma","mondo","0016982"
< "8761","megakaryocytic leukemia","icd10cm","C94.2"
< "8761","megakaryocytic leukemia","icd10cm","C94.20"
< "8761","megakaryocytic leukemia","icd9cm","207.2"
< "8761","megakaryocytic leukemia","mesh","D007947"
< "8761","megakaryocytic leukemia","umls","C0023462"
< "8761","megakaryocytic leukemia","mondo","0018872"
< "688","embryonal cancer","mesh","D009373"
< "688","embryonal cancer","umls","C0027654"
< "688","embryonal cancer","mondo","0005564"
< "7202","intermediate malignant teratoma","umls","C0334522"
< "7202","intermediate malignant teratoma","mondo","0004140"
< "684","hepatocellular carcinoma","icd10cm","C22.0"
< "684","hepatocellular carcinoma","mondo","0007256"
< "0060370","autosomal recessive early-onset Parkinson's disease 7","mondo","0011658"
< "1574","alcohol use disorder","icd10cm","F10.1"
< "1574","alcohol use disorder","icd9cm","305.0"
< "1574","alcohol use disorder","icd9cm","305.00"
< "1574","alcohol use disorder","mesh","D000437"
< "1574","alcohol use disorder","umls","C0085762"
< "1574","alcohol use disorder","mondo","0002046"
< "0050663","Bethlem myopathy","mondo","0008029"
< "0060652","familial erythrocytosis 1","icd10cm","D75.0"
< "0060652","familial erythrocytosis 1","mondo","0007572"
< "0060653","lethal congenital contracture syndrome 3","mondo","0012656"
< "0060655","autosomal recessive congenital ichthyosis","mesh","D016113"
< "0060655","autosomal recessive congenital ichthyosis","mesh","D017490"
< "0060655","autosomal recessive congenital ichthyosis","umls","C0079154"
< "0060655","autosomal recessive congenital ichthyosis","mondo","0017265"
< "0060656","autosomal recessive congenital ichthyosis 1","icd10cm","Q80.2"
< "0060656","autosomal recessive congenital ichthyosis 1","mondo","0009441"
< "3345","xanthomatosis","mesh","D014973"
< "3345","xanthomatosis","umls","C0043325"
< "3345","xanthomatosis","mondo","0002615"
< "13046","acute sphenoidal sinusitis","icd10cm","J01.3"
< "13046","acute sphenoidal sinusitis","icd10cm","J01.30"
< "13046","acute sphenoidal sinusitis","icd9cm","461.3"
< "13046","acute sphenoidal sinusitis","umls","C0155807"
< "13046","acute sphenoidal sinusitis","mondo","0001624"
---
> "7181","benign dermal neurilemmoma","umls","C1332490"
> "7181","benign dermal neurilemmoma","mondo","0004134"
> "7187","subacute lymphocytic thyroiditis","umls","C1306804"
> "7187","subacute lymphocytic thyroiditis","mondo","0004135"
> "0070034","autosomal dominant non-syndromic intellectual disability 4","mondo","0012947"
> "8549","chronic ulcer of skin","icd10cm","L98.4"
> "8549","chronic ulcer of skin","icd9cm","707"
> "8549","chronic ulcer of skin","umls","C0157738"
> "8549","chronic ulcer of skin","mondo","0004605"
> "3436","viral laryngitis","umls","C0853195"
> "3436","viral laryngitis","mondo","0002646"
> "12835","quadriplegia","icd10cm","G82.5"
> "12835","quadriplegia","icd10cm","G82.50"
> "12835","quadriplegia","icd9cm","344.00"
> "12835","quadriplegia","mesh","D011782"
> "12835","quadriplegia","umls","C0034372"
> "12835","quadriplegia","mondo","0001590"
> "0090090","hypogonadotropic hypogonadism 19 with or without anosmia","icd10cm","E23.0"
> "0090090","hypogonadotropic hypogonadism 19 with or without anosmia","mondo","0014105"
748,749c292,303
< "6293","central nervous system lipoma","umls","C1332885"
< "6293","central nervous system lipoma","mondo","0003844"
---
> "8012","benign pericardial teratoma","umls","C1334638"
> "8012","benign pericardial teratoma","mondo","0004432"
> "8543","Hodgkin's lymphoma, lymphocytic-histiocytic predominance","icd10cm","C81.4"
> "8543","Hodgkin's lymphoma, lymphocytic-histiocytic predominance","icd9cm","201.4"
> "8543","Hodgkin's lymphoma, lymphocytic-histiocytic predominance","mesh","D006689"
> "8543","Hodgkin's lymphoma, lymphocytic-histiocytic predominance","umls","C1266194"
> "8543","Hodgkin's lymphoma, lymphocytic-histiocytic predominance","mondo","0004604"
> "1222","cartilage disease","icd10cm","M91-M94"
> "1222","cartilage disease","icd10cm","M94.9"
> "1222","cartilage disease","mesh","D002357"
> "1222","cartilage disease","umls","C0007302"
> "1222","cartilage disease","mondo","0005569"
755,787c309,331
< "5629","adenosquamous colon carcinoma","umls","C1333082"
< "5629","adenosquamous colon carcinoma","mondo","0003554"
< "0110783","hereditary spastic paraplegia 32","icd10cm","G11.4"
< "0110783","hereditary spastic paraplegia 32","mondo","0012643"
< "5627","adenosquamous gallbladder carcinoma","umls","C1333741"
< "5627","adenosquamous gallbladder carcinoma","mondo","0006217"
< "5626","thymus adenosquamous carcinoma","umls","C1332171"
< "5626","thymus adenosquamous carcinoma","mondo","0003551"
< "5624","adenosquamous bile duct carcinoma","umls","C0861854"
< "5624","adenosquamous bile duct carcinoma","mondo","0003549"
< "4918","renal pelvis adenocarcinoma","umls","C1335748"
< "4918","renal pelvis adenocarcinoma","mondo","0003205"
< "0110780","hereditary spastic paraplegia 29","icd10cm","G11.4"
< "0110780","hereditary spastic paraplegia 29","mondo","0012334"
< "4385","papillary squamous carcinoma","umls","C0334244"
< "4385","papillary squamous carcinoma","mondo","0002979"
< "407","hepatic tuberculosis","mesh","D014386"
< "407","hepatic tuberculosis","umls","C0041313"
< "407","hepatic tuberculosis","mondo","0005787"
< "404","gastrointestinal tuberculosis","mesh","D014385"
< "404","gastrointestinal tuberculosis","umls","C0041312"
< "404","gastrointestinal tuberculosis","mondo","0005768"
< "402","oral tuberculosis","mesh","D014393"
< "402","oral tuberculosis","umls","C0041323"
< "402","oral tuberculosis","mondo","0005887"
< "7693","abdominal aortic aneurysm","mesh","D017544"
< "7693","abdominal aortic aneurysm","umls","C0162871"
< "7693","abdominal aortic aneurysm","mondo","0005350"
< "12217","Lewy body dementia","icd10cm","G31.83"
< "12217","Lewy body dementia","icd9cm","331.82"
< "12217","Lewy body dementia","mesh","D020961"
< "12217","Lewy body dementia","umls","C0752347"
< "12217","Lewy body dementia","mondo","0007488"
---
> "0111245","palmoplantar keratoderma and congenital alopecia 2","mesh","C535336"
> "0111245","palmoplantar keratoderma and congenital alopecia 2","umls","C1859316"
> "0110714","congenital stationary night blindness 1G","mondo","0014614"
> "0111246","amyotrophic lateral sclerosis-parkinsonism/dementia complex 1","umls","C0543859"
> "7459","acantholytic variant squamous cell breast carcinoma","umls","C1519485"
> "7459","acantholytic variant squamous cell breast carcinoma","mondo","0004229"
> "2742","auditory system disease","icd10cm","H93.9"
> "2742","auditory system disease","icd10cm","H93.90"
> "2742","auditory system disease","icd9cm","388.9"
> "2742","auditory system disease","mesh","D004427"
> "2742","auditory system disease","umls","C0013447"
> "2742","auditory system disease","mondo","0002409"
> "2536","chronic inflammatory demyelinating polyneuritis","icd10cm","G61.81"
> "2536","chronic inflammatory demyelinating polyneuritis","icd9cm","357.81"
> "2536","chronic inflammatory demyelinating polyneuritis","mesh","D020277"
> "2536","chronic inflammatory demyelinating polyneuritis","umls","C0393819"
> "2536","chronic inflammatory demyelinating polyneuritis","mondo","0002335"
> "0060019","coronin-1A deficiency","mondo","0014168"
> "2745","narcissistic personality disorder","icd10cm","F60.81"
> "2745","narcissistic personality disorder","icd9cm","301.81"
> "2745","narcissistic personality disorder","mesh","D010554"
> "2745","narcissistic personality disorder","umls","C0027402"
> "2745","narcissistic personality disorder","mondo","0002411"
793,808c337,350
< "12215","oligohydramnios","icd10cm","O41.0"
< "12215","oligohydramnios","icd10cm","O41.00"
< "12215","oligohydramnios","icd9cm","658.0"
< "12215","oligohydramnios","mesh","D016104"
< "12215","oligohydramnios","umls","C0079924"
< "12215","oligohydramnios","mondo","0005881"
< "0110959","Gaucher's disease type III","icd10cm","E75.2"
< "0110959","Gaucher's disease type III","mondo","0009267"
< "0070171","spermatogenic failure 12","mondo","0014172"
< "9463","otitis externa","icd9cm","380.1"
< "9463","otitis externa","icd9cm","380.10"
< "9463","otitis externa","umls","C0021355"
< "9463","otitis externa","mondo","0004795"
< "0110661","congenital myasthenic syndrome 20","mondo","0014939"
< "5997","non-proliferative fibrocystic change of the breast","umls","C1332628"
< "5997","non-proliferative fibrocystic change of the breast","mondo","0003724"
---
> "2747","glycogen storage disease","icd10cm","E74.0"
> "2747","glycogen storage disease","icd10cm","E74.00"
> "2747","glycogen storage disease","icd9cm","271.0"
> "2747","glycogen storage disease","mesh","D006008"
> "2747","glycogen storage disease","umls","C0017919"
> "2747","glycogen storage disease","mondo","0002412"
> "2746","glycogen storage disease V","icd10cm","E74.04"
> "2746","glycogen storage disease V","mesh","D006012"
> "2746","glycogen storage disease V","umls","C0017924"
> "2746","glycogen storage disease V","mondo","0009293"
> "2749","glycogen storage disease I","icd10cm","E74.01"
> "2749","glycogen storage disease I","mesh","D005953"
> "2749","glycogen storage disease I","umls","C0017920"
> "2749","glycogen storage disease I","mondo","0002413"
813a356,359
> "10880","iliac vein thrombophlebitis","icd10cm","I80.21"
> "10880","iliac vein thrombophlebitis","icd9cm","451.81"
> "10880","iliac vein thrombophlebitis","umls","C0155772"
> "10880","iliac vein thrombophlebitis","mondo","0001148"
824,914c370,389
< "10883","herpangina","icd10cm","B08.5"
< "10883","herpangina","icd9cm","074.0"
< "10883","herpangina","mesh","D006557"
< "10883","herpangina","umls","C0019338"
< "10883","herpangina","mondo","0005791"
< "11573","listeriosis","icd10cm","A32"
< "11573","listeriosis","icd10cm","A32.9"
< "11573","listeriosis","icd9cm","027.0"
< "11573","listeriosis","mesh","D008088"
< "11573","listeriosis","umls","C0023860"
< "11573","listeriosis","mondo","0005828"
< "5998","microglandular adenosis","mesh","D005348"
< "5998","microglandular adenosis","umls","C0085750"
< "5998","microglandular adenosis","mondo","0003725"
< "4737","somatoform disorder","icd10cm","F45"
< "4737","somatoform disorder","icd10cm","F45.0"
< "4737","somatoform disorder","icd10cm","F45.9"
< "4737","somatoform disorder","icd9cm","300.8"
< "4737","somatoform disorder","icd9cm","300.81"
< "4737","somatoform disorder","mesh","D013001"
< "4737","somatoform disorder","umls","C0037650"
< "4737","somatoform disorder","umls","C0520482"
< "4737","somatoform disorder","mondo","0003117"
< "0110789","hereditary spastic paraplegia 38","icd10cm","G11.4"
< "0110789","hereditary spastic paraplegia 38","mondo","0012867"
< "11379","gnathomiasis","icd10cm","B83.1"
< "11379","gnathomiasis","icd9cm","128.1"
< "11379","gnathomiasis","mesh","D058429"
< "11379","gnathomiasis","umls","C0018013"
< "11379","gnathomiasis","mondo","0005776"
< "11372","megacolon","icd10cm","K59.3"
< "11372","megacolon","icd10cm","K59.39"
< "11372","megacolon","mesh","D008531"
< "11372","megacolon","umls","C0025160"
< "11372","megacolon","mondo","0001273"
< "0110953","Waardenburg syndrome type 4A","mondo","0010192"
< "5078","ganglioglioma","mesh","D018303"
< "5078","ganglioglioma","umls","C0206716"
< "5078","ganglioglioma","umls","C1332202"
< "5078","ganglioglioma","umls","C1332969"
< "5078","ganglioglioma","mondo","0016733"
< "6212","ovarian endometrial cancer","umls","C1335159"
< "6212","ovarian endometrial cancer","umls","C1518231"
< "6212","ovarian endometrial cancer","mondo","0003812"
< "7527","acute gonococcal endometritis","icd9cm","098.16"
< "7527","acute gonococcal endometritis","umls","C0153196"
< "7527","acute gonococcal endometritis","mondo","0004264"
< "0110666","congenital myasthenic syndrome 3A","mondo","0014583"
< "374","nutrition disease","mesh","D009748"
< "374","nutrition disease","umls","C3714509"
< "374","nutrition disease","mondo","0005137"
< "0060900","autosomal recessive Parkinson's disease 14","mesh","C567844"
< "0060900","autosomal recessive Parkinson's disease 14","mondo","0013060"
< "0060901","Waldenstroem's macroglobulinemia","icd10cm","C88.0"
< "0060901","Waldenstroem's macroglobulinemia","icd9cm","273.3"
< "0060901","Waldenstroem's macroglobulinemia","mesh","D008258"
< "0060901","Waldenstroem's macroglobulinemia","umls","C0024419"
< "0060901","Waldenstroem's macroglobulinemia","mondo","0007926"
< "0060902","Norman-Roberts syndrome","mesh","C537848"
< "0060902","Norman-Roberts syndrome","umls","C0796089"
< "0060902","Norman-Roberts syndrome","mondo","0009760"
< "13608","biliary atresia","icd10cm","Q44.2"
< "13608","biliary atresia","icd9cm","751.61"
< "13608","biliary atresia","mesh","D001656"
< "13608","biliary atresia","umls","C0005411"
< "13608","biliary atresia","mondo","0008867"
< "0110574","autosomal dominant nonsyndromic deafness 4B","icd10cm","H90.3"
< "0110574","autosomal dominant nonsyndromic deafness 4B","mondo","0013823"
< "891","progressive myoclonus epilepsy","mesh","D020191"
< "891","progressive myoclonus epilepsy","umls","C0751778"
< "891","progressive myoclonus epilepsy","mondo","0020074"
< "0050760","X-linked myopathy with excessive autophagy","mondo","0010684"
< "2312","nocardiosis","icd10cm","A43"
< "2312","nocardiosis","icd10cm","A43.9"
< "2312","nocardiosis","mesh","D009617"
< "2312","nocardiosis","umls","C0028242"
< "2312","nocardiosis","mondo","0017776"
< "0090088","hypogonadotropic hypogonadism 24 without anosmia","icd10cm","E23.6"
< "0090088","hypogonadotropic hypogonadism 24 without anosmia","mondo","0009239"
< "6652","diffuse idiopathic skeletal hyperostosis","icd10cm","M48.1"
< "6652","diffuse idiopathic skeletal hyperostosis","icd9cm","721.6"
< "6652","diffuse idiopathic skeletal hyperostosis","mesh","D004057"
< "6652","diffuse idiopathic skeletal hyperostosis","umls","C0020498"
< "6652","diffuse idiopathic skeletal hyperostosis","mondo","0007127"
< "12712","nephronophthisis","icd10cm","Q61.5"
< "12712","nephronophthisis","umls","C0687120"
< "12712","nephronophthisis","mondo","0019005"
< "12716","newborn respiratory distress syndrome","icd10cm","P22.0"
< "12716","newborn respiratory distress syndrome","mesh","D006819"
< "12716","newborn respiratory distress syndrome","umls","C0020192"
< "12716","newborn respiratory distress syndrome","mondo","0009971"
---
> "2748","glycogen storage disease III","icd10cm","E74.03"
> "2748","glycogen storage disease III","mesh","D006010"
> "2748","glycogen storage disease III","umls","C0017922"
> "2748","glycogen storage disease III","mondo","0009291"
> "0110665","congenital myasthenic syndrome 3B","mondo","0014584"
> "0080256","Perrault syndrome 6","mondo","0033047"
> "0080257","autosomal recessive congenital ichthyosis 13","mondo","0033092"
> "0080254","orofaciodigital syndrome XVI","mondo","0033045"
> "0080255","Meier-Gorlin syndrome 8","mondo","0033046"
> "0080252","spastic ataxia 8","mondo","0033043"
> "0080253","Meckel syndrome 13","mondo","0033044"
> "0080250","erythrokeratodermia variabilis et progressiva 4","mondo","0033014"
> "0080251","erythrokeratodermia variabilis et progressiva 5","mondo","0033015"
> "0080258","autosomal recessive congenital ichthyosis 14","mondo","0033091"
> "0080259","autosomal recessive spinocerebellar ataxia 25","mondo","0033115"
> "0110042","Alzheimer's disease 3","mondo","0011913"
> "397","restrictive cardiomyopathy","icd10cm","I42.5"
> "397","restrictive cardiomyopathy","mesh","D002313"
> "397","restrictive cardiomyopathy","umls","C0007196"
> "397","restrictive cardiomyopathy","mondo","0005201"
918,954c393,419
< "0070262","congenital disorder of glycosylation type IIj","mondo","0013281"
< "12718","chronic gonococcal salpingitis","icd9cm","098.37"
< "12718","chronic gonococcal salpingitis","umls","C0153208"
< "12718","chronic gonococcal salpingitis","mondo","0001575"
< "0110954","Waardenburg syndrome type 4B","mondo","0013201"
< "0050664","Bietti crystalline corneoretinal dystrophy","mondo","0008865"
< "10970","spastic quadriplegia","icd9cm","343.2"
< "10970","spastic quadriplegia","mesh","D002547"
< "10970","spastic quadriplegia","umls","C0154697"
< "10970","spastic quadriplegia","mondo","0016215"
< "0110949","Waardenburg syndrome type 3","icd10cm","E70.3"
< "0110949","Waardenburg syndrome type 3","mondo","0007862"
< "896","metal metabolism disorder","mesh","D008664"
< "896","metal metabolism disorder","umls","C0025534"
< "896","metal metabolism disorder","mondo","0004689"
< "6787","childhood vagina botryoid rhabdomyosarcoma","umls","C1332945"
< "6787","childhood vagina botryoid rhabdomyosarcoma","mondo","0003993"
< "6786","childhood botryoid rhabdomyosarcoma","umls","C1332944"
< "6786","childhood botryoid rhabdomyosarcoma","mondo","0003992"
< "0110940","autosomal recessive osteopetrosis 8","mondo","0014040"
< "0110941","autosomal recessive osteopetrosis 3","mondo","0009818"
< "0110942","autosomal recessive osteopetrosis 1","mondo","0009815"
< "0110943","autosomal recessive osteopetrosis 2","mondo","0009816"
< "0110944","autosomal recessive osteopetrosis 4","mondo","0012676"
< "0110945","autosomal recessive osteopetrosis 6","mondo","0012679"
< "0110946","autosomal recessive osteopetrosis 7","icd10cm","Q78.2"
< "0110946","autosomal recessive osteopetrosis 7","mondo","0012859"
< "0110947","Waardenburg syndrome type 2B","mondo","0010841"
< "11289","ventilation pneumonitis","icd10cm","J67.7"
< "11289","ventilation pneumonitis","icd9cm","495.7"
< "11289","ventilation pneumonitis","umls","C0155891"
< "11289","ventilation pneumonitis","mondo","0001255"
< "898","autosomal dominant polycystic kidney disease","icd10cm","Q61.3"
< "898","autosomal dominant polycystic kidney disease","icd9cm","753.12"
< "898","autosomal dominant polycystic kidney disease","mesh","D007690"
< "898","autosomal dominant polycystic kidney disease","umls","C0022680"
< "898","autosomal dominant polycystic kidney disease","mondo","0004691"
---
> "399","tuberculosis","mesh","D014375"
> "399","tuberculosis","umls","C0041295"
> "399","tuberculosis","mondo","0018076"
> "13619","extrahepatic cholestasis","mesh","D001651"
> "13619","extrahepatic cholestasis","umls","C0005398"
> "13619","extrahepatic cholestasis","mondo","0006757"
> "2301","atrophy of prostate","icd9cm","602.2"
> "2301","atrophy of prostate","umls","C0156296"
> "2301","atrophy of prostate","mondo","0002264"
> "4724","brain edema","mesh","D001929"
> "4724","brain edema","umls","C1527311"
> "4724","brain edema","mondo","0006684"
> "2303","stereotypic movement disorder","icd10cm","F98.4"
> "2303","stereotypic movement disorder","icd9cm","307.3"
> "2303","stereotypic movement disorder","mesh","D019956"
> "2303","stereotypic movement disorder","umls","C0038273"
> "2303","stereotypic movement disorder","mondo","0002265"
> "4723","intracranial hypotension","mesh","D019585"
> "4723","intracranial hypotension","umls","C0524812"
> "4723","intracranial hypotension","mondo","0006811"
> "5847","posterior myocardial infarction","umls","C0340319"
> "5847","posterior myocardial infarction","mondo","0003672"
> "5846","septal myocardial infarction","umls","C0746727"
> "5846","septal myocardial infarction","mondo","0003671"
> "5845","anterolateral myocardial infarction","mesh","D056988"
> "5845","anterolateral myocardial infarction","umls","C0262564"
> "5845","anterolateral myocardial infarction","mondo","0006652"
960,965c425,443
< "0050757","deafness-dystonia-optic neuronopathy syndrome","mesh","C535808"
< "0050757","deafness-dystonia-optic neuronopathy syndrome","mondo","0010578"
< "0050752","amyotrophic lateral sclerosis type 8","mondo","0012077"
< "963","episodic ataxia","mesh","C580065"
< "963","episodic ataxia","umls","C1720189"
< "963","episodic ataxia","mondo","0016227"
---
> "5843","posteroinferior myocardial infarction","umls","C3642318"
> "5843","posteroinferior myocardial infarction","mondo","0003670"
> "5842","testis seminoma","mesh","D018239"
> "5842","testis seminoma","umls","C0036631"
> "5842","testis seminoma","mondo","0003669"
> "11283","peripheral scars of retina","icd9cm","363.34"
> "11283","peripheral scars of retina","umls","C0154888"
> "11283","peripheral scars of retina","mondo","0001254"
> "11282","solar retinopathy","icd10cm","H31.02"
> "11282","solar retinopathy","icd9cm","363.31"
> "11282","solar retinopathy","umls","C0152131"
> "11282","solar retinopathy","mondo","0001253"
> "11285","tick paralysis","mesh","D013985"
> "11285","tick paralysis","umls","C0040197"
> "11285","tick paralysis","mondo","0005981"
> "5849","subendocardial myocardial infarction","umls","C3642476"
> "5849","subendocardial myocardial infarction","mondo","0003674"
> "5848","apical myocardial infarction","umls","C3642319"
> "5848","apical myocardial infarction","mondo","0003673"
968a447,448
> "3747","esophagus verrucous carcinoma","umls","C1333470"
> "3747","esophagus verrucous carcinoma","mondo","0002762"
971,973d450
< "299","adenocarcinoma","mesh","D000230"
< "299","adenocarcinoma","umls","C0001418"
< "299","adenocarcinoma","mondo","0004970"
975a453,454
> "3743","cervical verrucous carcinoma","umls","C1516435"
> "3743","cervical verrucous carcinoma","mondo","0002761"
978,985c457,458
< "0050759","myotonic dystrophy type 2","icd10cm","G71.1"
< "0050759","myotonic dystrophy type 2","icd10cm","G71.19"
< "0050759","myotonic dystrophy type 2","icd9cm","359.2"
< "0050759","myotonic dystrophy type 2","mesh","D020967"
< "0050759","myotonic dystrophy type 2","umls","C0221055"
< "0050759","myotonic dystrophy type 2","umls","C0553604"
< "0050759","myotonic dystrophy type 2","umls","C0752355"
< "0050759","myotonic dystrophy type 2","mondo","0011266"
---
> "3741","bladder verrucous squamous cell carcinoma","umls","C1511208"
> "3741","bladder verrucous squamous cell carcinoma","mondo","0002759"
995,1082c468,528
< "11156","anhidrosis","icd10cm","L74.4"
< "11156","anhidrosis","icd9cm","705.0"
< "11156","anhidrosis","mesh","D007007"
< "11156","anhidrosis","umls","C0003028"
< "11156","anhidrosis","mondo","0006527"
< "0060838","isolated microphthalmia 7","icd10cm","Q11.0"
< "0060838","isolated microphthalmia 7","mondo","0013377"
< "0060839","isolated microphthalmia 2","icd10cm","Q11.0"
< "0060839","isolated microphthalmia 2","mondo","0012409"
< "0060834","Griscelli syndrome type 3","mesh","C537303"
< "0060834","Griscelli syndrome type 3","umls","C1836573"
< "0060834","Griscelli syndrome type 3","mondo","0012220"
< "0060835","isolated microphthalmia 6","icd10cm","Q11.0"
< "0060835","isolated microphthalmia 6","mondo","0013293"
< "0060836","isolated microphthalmia 4","icd10cm","Q11.0"
< "0060836","isolated microphthalmia 4","mondo","0013130"
< "0110806","hereditary spastic paraplegia 54","icd10cm","G11.4"
< "0110806","hereditary spastic paraplegia 54","mondo","0014018"
< "0060830","deafness-intellectual disability, Martin-Probst type syndrome","icd10cm","Q87.8"
< "0060830","deafness-intellectual disability, Martin-Probst type syndrome","mondo","0010353"
< "0060831","Griscelli syndrome","icd10cm","E70.3"
< "0060831","Griscelli syndrome","mondo","0018306"
< "0110803","hereditary spastic paraplegia 51","mondo","0013401"
< "0110802","hereditary spastic paraplegia 50","mondo","0013048"
< "0111046","platelet-type bleeding disorder 10","mondo","0012031"
< "0111047","platelet-type bleeding disorder 14","mondo","0013597"
< "0111044","gray platelet syndrome","icd10cm","D69.1"
< "0111044","gray platelet syndrome","mesh","D055652"
< "0111044","gray platelet syndrome","umls","C0272302"
< "0111044","gray platelet syndrome","mondo","0007686"
< "0111045","platelet-type bleeding disorder 9","icd10cm","D69.8"
< "0111045","platelet-type bleeding disorder 9","mondo","0013622"
< "201","connective tissue cancer","mesh","D009372"
< "201","connective tissue cancer","umls","C0027656"
< "201","connective tissue cancer","mondo","0002176"
< "0111043","glycogen storage disease IXc","icd10cm","E74.0"
< "0111043","glycogen storage disease IXc","mondo","0013091"
< "0111040","glycogen storage disease IXd","icd10cm","E74.0"
< "0111040","glycogen storage disease IXd","mondo","0010362"
< "0111041","glycogen storage disease IXb","icd10cm","E74.0"
< "0111041","glycogen storage disease IXb","mondo","0009868"
< "12002","trachea sarcoma","umls","C1336774"
< "12002","trachea sarcoma","mondo","0001418"
< "12003","trachea squamous cell carcinoma","umls","C0345946"
< "12003","trachea squamous cell carcinoma","mondo","0001419"
< "0111048","platelet-type bleeding disorder 19","icd10cm","D69.4"
< "0111048","platelet-type bleeding disorder 19","mondo","0014518"
< "0111049","platelet-type bleeding disorder 17","icd10cm","D69.1"
< "0111049","platelet-type bleeding disorder 17","mesh","D055652"
< "0111049","platelet-type bleeding disorder 17","umls","C0272302"
< "0111049","platelet-type bleeding disorder 17","mondo","0008553"
< "5529","lacrimal gland squamous cell carcinoma","umls","C1334360"
< "5529","lacrimal gland squamous cell carcinoma","mondo","0003492"
< "0040006","carbamazepine allergy","umls","C0570787"
< "9249","Beemer-Langer syndrome","mesh","C537599"
< "9249","Beemer-Langer syndrome","umls","C0432198"
< "9249","Beemer-Langer syndrome","mondo","0010024"
< "0050133","superficial mycosis","icd10cm","B36.9"
< "0050133","superficial mycosis","mesh","D010854"
< "0050133","superficial mycosis","umls","C0031898"
< "0050133","superficial mycosis","umls","C2980104"
< "0050133","superficial mycosis","mondo","0024268"
< "0070288","primary autosomal recessive microcephaly 17","mondo","0014908"
< "0070289","primary autosomal recessive microcephaly 16","mondo","0014730"
< "0040005","ceftriaxone allergy","umls","C0571463"
< "125","vagina leiomyoma","umls","C1336939"
< "125","vagina leiomyoma","mondo","0001536"
< "9538","multiple myeloma","icd10cm","C90.0"
< "9538","multiple myeloma","icd10cm","C90.00"
< "9538","multiple myeloma","icd9cm","203.0"
< "9538","multiple myeloma","mesh","D009101"
< "9538","multiple myeloma","umls","C0026764"
< "9538","multiple myeloma","mondo","0009693"
< "0070282","primary autosomal recessive microcephaly 8","mondo","0013849"
< "0070283","primary autosomal recessive microcephaly 13","mondo","0014473"
< "0070280","primary autosomal recessive microcephaly 5","mondo","0012106"
< "0070281","primary autosomal recessive microcephaly 19","mondo","0054716"
< "0070286","primary autosomal recessive microcephaly 3","mondo","0011488"
< "0070287","primary autosomal recessive microcephaly 11","mondo","0014173"
< "0070284","primary autosomal recessive microcephaly 12","mondo","0014484"
< "0070285","primary autosomal recessive microcephaly 1","mondo","0009617"
< "0090136","complex cortical dysplasia with other brain malformations 6","mondo","0014341"
< "0050463","campomelic dysplasia","mesh","D055036"
< "0050463","campomelic dysplasia","umls","C1861922"
< "0050463","campomelic dysplasia","umls","C1861923"
< "0050463","campomelic dysplasia","mondo","0007251"
< "0070048","autosomal dominant non-syndromic intellectual disability 18","mondo","0014034"
< "0070049","autosomal dominant non-syndromic intellectual disability 19","mondo","0014035"
---
> "4624","Ollier disease","icd10cm","Q78.4"
> "4624","Ollier disease","mesh","D004687"
> "4624","Ollier disease","umls","C0024454"
> "4624","Ollier disease","mondo","0008145"
> "13534","purulent labyrinthitis","icd9cm","386.33"
> "13534","purulent labyrinthitis","umls","C0155506"
> "13534","purulent labyrinthitis","mondo","0001739"
> "4626","hydranencephaly","icd10cm","Q04.3"
> "4626","hydranencephaly","mesh","D006832"
> "4626","hydranencephaly","umls","C0020225"
> "4626","hydranencephaly","mondo","0016344"
> "4627","ideomotor apraxia","mesh","D020240"
> "4627","ideomotor apraxia","umls","C0234523"
> "4627","ideomotor apraxia","mondo","0006800"
> "13538","cornea squamous cell carcinoma","umls","C0346366"
> "13538","cornea squamous cell carcinoma","mondo","0001740"
> "11755","choledocholithiasis","mesh","D042883"
> "11755","choledocholithiasis","umls","C0701818"
> "11755","choledocholithiasis","mondo","0006699"
> "11754","siderosis of eye","icd10cm","H44.32"
> "11754","siderosis of eye","icd9cm","360.23"
> "11754","siderosis of eye","umls","C0271001"
> "11754","siderosis of eye","mondo","0001355"
> "11752","acute endophthalmitis","icd9cm","360.01"
> "11752","acute endophthalmitis","umls","C0154773"
> "11752","acute endophthalmitis","mondo","0017202"
> "0040002","aspirin allergy","umls","C0004058"
> "0040002","aspirin allergy","mondo","0025518"
> "11759","hypochromic anemia","icd10cm","D50"
> "11759","hypochromic anemia","mesh","D000747"
> "11759","hypochromic anemia","umls","C0002884"
> "11759","hypochromic anemia","mondo","0001357"
> "11758","iron deficiency anemia","icd9cm","280.8"
> "11758","iron deficiency anemia","umls","C0029810"
> "11758","iron deficiency anemia","mondo","0001356"
> "14534","malignant cardiac peripheral nerve sheath neoplasm","umls","C1334569"
> "14534","malignant cardiac peripheral nerve sheath neoplasm","mondo","0001990"
> "14535","malignant cardiac germ cell tumor","umls","C1334566"
> "14535","malignant cardiac germ cell tumor","mondo","0001991"
> "5204","fructose-1,6-bisphosphatase deficiency","icd10cm","E74.19"
> "5204","fructose-1,6-bisphosphatase deficiency","mesh","D015319"
> "5204","fructose-1,6-bisphosphatase deficiency","umls","C0016756"
> "5204","fructose-1,6-bisphosphatase deficiency","mondo","0009251"
> "3773","third ventricle chordoid glioma","umls","C1322252"
> "3773","third ventricle chordoid glioma","mondo","0016706"
> "200","giant cell tumor","mesh","D005870"
> "200","giant cell tumor","umls","C0017525"
> "200","giant cell tumor","mondo","0002171"
> "5207","monodermal teratoma","umls","C1302569"
> "5207","monodermal teratoma","mondo","0003331"
> "3772","intraventricular meningioma","mesh","D008579"
> "3772","intraventricular meningioma","umls","C1334271"
> "3772","intraventricular meningioma","mondo","0002772"
> "11991","osteopoikilosis","icd10cm","Q78.8"
> "11991","osteopoikilosis","icd9cm","756.53"
> "11991","osteopoikilosis","mesh","D010023"
> "11991","osteopoikilosis","umls","C0029455"
> "11991","osteopoikilosis","mondo","0001414"
> "3770","pulmonary fibrosis","mesh","D011658"
> "3770","pulmonary fibrosis","umls","C0034069"
> "3770","pulmonary fibrosis","mondo","0002771"
1094,1095c540,543
< "0070044","Coffin-Siris syndrome 2","mondo","0013819"
< "0070045","Coffin-Siris syndrome 3","mondo","0013820"
---
> "3777","granuloma annulare","icd10cm","L92.0"
> "3777","granuloma annulare","mesh","D016460"
> "3777","granuloma annulare","umls","C0085074"
> "3777","granuloma annulare","mondo","0006554"
1105,1108c553,563
< "0070047","Schuurs-Hoeijmakers Syndrome","mondo","0014006"
< "0070040","autosomal dominant non-syndromic intellectual disability 10","mondo","0013657"
< "0070041","autosomal dominant non-syndromic intellectual disability 11","mondo","0013658"
< "0070042","Coffin-Siris syndrome 1","mondo","0013804"
---
> "174","acanthoma","mesh","D049309"
> "174","acanthoma","umls","C0846967"
> "174","acanthoma","mondo","0002093"
> "173","eccrine sweat gland neoplasm","umls","C1333371"
> "173","eccrine sweat gland neoplasm","mondo","0002090"
> "13282","intestinal tuberculosis","icd9cm","014.8"
> "13282","intestinal tuberculosis","umls","C0152724"
> "13282","intestinal tuberculosis","mondo","0001678"
> "171","neuroectodermal tumor","mesh","D017599"
> "171","neuroectodermal tumor","umls","C0206093"
> "171","neuroectodermal tumor","mondo","0005462"
1115,1225c570,590
< "2050","acute maxillary sinusitis","icd10cm","J01.0"
< "2050","acute maxillary sinusitis","icd10cm","J01.00"
< "2050","acute maxillary sinusitis","icd9cm","461.0"
< "2050","acute maxillary sinusitis","umls","C0155804"
< "2050","acute maxillary sinusitis","mondo","0002186"
< "3200","cerebellopontine angle tumor","mondo","0002553"
< "2055","post-traumatic stress disorder","icd10cm","F43.1"
< "2055","post-traumatic stress disorder","icd10cm","F43.10"
< "2055","post-traumatic stress disorder","icd9cm","309.81"
< "2055","post-traumatic stress disorder","mesh","D013313"
< "2055","post-traumatic stress disorder","umls","C0038436"
< "2055","post-traumatic stress disorder","mondo","0005146"
< "4829","adenosquamous lung carcinoma","umls","C0279557"
< "4829","adenosquamous lung carcinoma","mondo","0004973"
< "4534","Hallermann-Streiff syndrome","mesh","D006210"
< "4534","Hallermann-Streiff syndrome","umls","C0018522"
< "4534","Hallermann-Streiff syndrome","mondo","0009318"
< "2058","chronic mucocutaneous candidiasis","mesh","D002178"
< "2058","chronic mucocutaneous candidiasis","umls","C0006845"
< "2058","chronic mucocutaneous candidiasis","mondo","0015279"
< "3692","anal canal adenocarcinoma","umls","C1332259"
< "3692","anal canal adenocarcinoma","mondo","0002735"
< "0111007","X-linked cone-rod dystrophy 3","mondo","0010335"
< "4531","mucoepidermoid carcinoma","mesh","D018277"
< "4531","mucoepidermoid carcinoma","umls","C0206694"
< "4531","mucoepidermoid carcinoma","mondo","0003036"
< "3697","acute transudative otitis media","icd9cm","381.0"
< "3697","acute transudative otitis media","icd9cm","381.00"
< "3697","acute transudative otitis media","umls","C0271432"
< "3697","acute transudative otitis media","mondo","0002738"
< "10629","microphthalmia","icd10cm","Q11.2"
< "10629","microphthalmia","icd9cm","743.1"
< "10629","microphthalmia","icd9cm","743.10"
< "10629","microphthalmia","icd9cm","743.11"
< "10629","microphthalmia","mesh","D008850"
< "10629","microphthalmia","umls","C0026010"
< "10629","microphthalmia","mondo","0021129"
< "12139","dysthymic disorder","icd10cm","F34.1"
< "12139","dysthymic disorder","icd9cm","300.4"
< "12139","dysthymic disorder","mesh","D019263"
< "12139","dysthymic disorder","umls","C0013415"
< "12139","dysthymic disorder","mondo","0001442"
< "9406","hypopituitarism","icd10cm","E23.0"
< "9406","hypopituitarism","mesh","D007018"
< "9406","hypopituitarism","umls","C0020635"
< "9406","hypopituitarism","mondo","0005152"
< "0070023","autosomal dominant dyskeratosis congenita 6","mondo","0014690"
< "12132","granulomatosis with polyangiitis","icd10cm","M31.3"
< "12132","granulomatosis with polyangiitis","icd10cm","M31.30"
< "12132","granulomatosis with polyangiitis","icd9cm","446.4"
< "12132","granulomatosis with polyangiitis","mesh","D014890"
< "12132","granulomatosis with polyangiitis","umls","C3495801"
< "12132","granulomatosis with polyangiitis","mondo","0012105"
< "6367","acral lentiginous melanoma","mondo","0003865"
< "12134","factor VIII deficiency","icd10cm","D66"
< "12134","factor VIII deficiency","icd9cm","286.0"
< "12134","factor VIII deficiency","mesh","D006467"
< "12134","factor VIII deficiency","umls","C0019069"
< "12134","factor VIII deficiency","mondo","0010602"
< "6364","migraine","icd10cm","G43"
< "6364","migraine","icd10cm","G43.9"
< "6364","migraine","icd10cm","G43.909"
< "6364","migraine","icd9cm","346"
< "6364","migraine","icd9cm","346.9"
< "6364","migraine","mesh","D008881"
< "6364","migraine","umls","C0042331"
< "6364","migraine","umls","C0149931"
< "6364","migraine","mondo","0005277"
< "10153","ileum cancer","icd10cm","C17.2"
< "10153","ileum cancer","icd9cm","152.2"
< "10153","ileum cancer","umls","C0153428"
< "10153","ileum cancer","mondo","0000955"
< "10155","intestinal cancer","icd10cm","C26.0"
< "10155","intestinal cancer","icd9cm","159.0"
< "10155","intestinal cancer","mesh","D007414"
< "10155","intestinal cancer","umls","C0346627"
< "10155","intestinal cancer","mondo","0005814"
< "10159","osteonecrosis","icd10cm","M87"
< "10159","osteonecrosis","icd10cm","M87.9"
< "10159","osteonecrosis","icd9cm","732.3"
< "10159","osteonecrosis","icd9cm","733.41"
< "10159","osteonecrosis","icd9cm","733.42"
< "10159","osteonecrosis","icd9cm","733.43"
< "10159","osteonecrosis","icd9cm","733.44"
< "10159","osteonecrosis","mesh","D010020"
< "10159","osteonecrosis","umls","C0003977"
< "10159","osteonecrosis","umls","C0027543"
< "10159","osteonecrosis","umls","C0029445"
< "10159","osteonecrosis","umls","C0158442"
< "10159","osteonecrosis","umls","C0158449"
< "10159","osteonecrosis","umls","C0158450"
< "10159","osteonecrosis","umls","C0158451"
< "10159","osteonecrosis","umls","C0745048"
< "10159","osteonecrosis","mondo","0005380"
< "11976","botulism","icd10cm","A05.1"
< "11976","botulism","mesh","D001906"
< "11976","botulism","umls","C0006057"
< "11976","botulism","mondo","0005498"
< "3526","cerebral infarction","icd10cm","I63"
< "3526","cerebral infarction","icd10cm","I63.9"
< "3526","cerebral infarction","mesh","D002544"
< "3526","cerebral infarction","umls","C0007785"
< "3526","cerebral infarction","mondo","0002679"
< "3522","lateral medullary syndrome","icd10cm","G46.3"
< "3522","lateral medullary syndrome","mesh","D014854"
< "3522","lateral medullary syndrome","umls","C0043019"
< "3522","lateral medullary syndrome","mondo","0006827"
< "0070024","autosomal recessive dyskeratosis congenita 6","mondo","0014600"
< "0050628","advanced sleep phase syndrome","mondo","0015609"
< "0050629","Aicardi-Goutieres syndrome","icd10cm","G31.8"
< "0050629","Aicardi-Goutieres syndrome","mondo","0018866"
---
> "203","exostosis","icd10cm","M27.8"
> "203","exostosis","icd9cm","726.91"
> "203","exostosis","mesh","D005096"
> "203","exostosis","umls","C1442903"
> "203","exostosis","mondo","0002181"
> "3774","chordoid glioma","umls","C1322252"
> "3774","chordoid glioma","mondo","0016706"
> "14165","bilateral hyperactive labyrinth","icd9cm","386.52"
> "14165","bilateral hyperactive labyrinth","umls","C0155516"
> "14165","bilateral hyperactive labyrinth","mondo","0001897"
> "0110445","dilated cardiomyopathy 1KK","icd10cm","I42.0"
> "0110445","dilated cardiomyopathy 1KK","mondo","0014100"
> "0110444","dilated cardiomyopathy 1X","icd10cm","I42.0"
> "0110444","dilated cardiomyopathy 1X","mondo","0012704"
> "10393","secondary hypertrophic osteoarthropathy","icd10cm","M89.4"
> "10393","secondary hypertrophic osteoarthropathy","icd9cm","731.2"
> "10393","secondary hypertrophic osteoarthropathy","mesh","D010005"
> "10393","secondary hypertrophic osteoarthropathy","umls","C0029412"
> "10393","secondary hypertrophic osteoarthropathy","mondo","0006965"
> "0110716","Warburg micro syndrome 1","icd10cm","Q87.0"
> "0110716","Warburg micro syndrome 1","mondo","0010822"
1235,1238c600,602
< "0070255","congenital disorder of glycosylation type IIc","umls","C0398739"
< "0070255","congenital disorder of glycosylation type IIc","mondo","0009953"
< "0050625","biliary tract benign neoplasm","umls","C0345913"
< "0050625","biliary tract benign neoplasm","mondo","0005304"
---
> "10399","seminal vesicle chronic gonorrhea","icd9cm","098.34"
> "10399","seminal vesicle chronic gonorrhea","umls","C0153205"
> "10399","seminal vesicle chronic gonorrhea","mondo","0001025"
1251,1256c615
< "3541","cerebral ventricle cancer","icd10cm","C71.5"
< "3541","cerebral ventricle cancer","icd9cm","191.5"
< "3541","cerebral ventricle cancer","mesh","D002551"
< "3541","cerebral ventricle cancer","umls","C0007798"
< "3541","cerebral ventricle cancer","umls","C0346906"
< "3541","cerebral ventricle cancer","mondo","0002682"
---
> "0110440","dilated cardiomyopathy 1J","mondo","0011541"
1269,1270c628,629
< "0110155","Charcot-Marie-Tooth disease type 2A2","icd10cm","G60.0"
< "0110155","Charcot-Marie-Tooth disease type 2A2","mondo","0012231"
---
> "0110155","Charcot-Marie-Tooth disease type 2A2A","icd10cm","G60.0"
> "0110155","Charcot-Marie-Tooth disease type 2A2A","mondo","0012231"
1273,1276c632,645
< "0110159","Charcot-Marie-Tooth disease type 2B","icd10cm","G60.0"
< "0110159","Charcot-Marie-Tooth disease type 2B","mondo","0010949"
< "0110158","Charcot-Marie-Tooth disease type 2I","icd10cm","G60.0"
< "0110158","Charcot-Marie-Tooth disease type 2I","mondo","0011889"
---
> "7210","psammomatous meningioma","mesh","D008579"
> "7210","psammomatous meningioma","umls","C0334607"
> "7210","psammomatous meningioma","mondo","0004143"
> "7211","fibrous meningioma","mesh","D008579"
> "7211","fibrous meningioma","umls","C0334606"
> "7211","fibrous meningioma","mondo","0004144"
> "7212","meningothelial meningioma","mesh","D008579"
> "7212","meningothelial meningioma","umls","C0334605"
> "7212","meningothelial meningioma","mondo","0004145"
> "7213","transitional meningioma","mesh","D008579"
> "7213","transitional meningioma","umls","C0334611"
> "7213","transitional meningioma","mondo","0004146"
> "7214","noninvasive malignant thymoma","umls","C0278847"
> "7214","noninvasive malignant thymoma","mondo","0004147"
1279,1286c648,650
< "3594","choriocarcinoma","icd10cm","C58"
< "3594","choriocarcinoma","mesh","D002822"
< "3594","choriocarcinoma","umls","C0008497"
< "3594","choriocarcinoma","mondo","0005207"
< "0110794","hereditary spastic paraplegia 42","icd10cm","G11.4"
< "0110794","hereditary spastic paraplegia 42","mondo","0012928"
< "0110797","hereditary spastic paraplegia 45","icd10cm","G11.4"
< "0110797","hereditary spastic paraplegia 45","mondo","0013165"
---
> "6217","gastric diffuse adenocarcinoma","umls","C0279635"
> "6217","gastric diffuse adenocarcinoma","umls","C0334280"
> "6217","gastric diffuse adenocarcinoma","mondo","0005017"
1289,1311c653,659
< "0110791","hereditary spastic paraplegia 3A","icd10cm","G11.4"
< "0110791","hereditary spastic paraplegia 3A","mondo","0008437"
< "0110790","hereditary spastic paraplegia 39","icd10cm","G11.4"
< "0110790","hereditary spastic paraplegia 39","mondo","0012787"
< "0110793","hereditary spastic paraplegia 41","icd10cm","G11.4"
< "0110793","hereditary spastic paraplegia 41","mondo","0013239"
< "0110792","hereditary spastic paraplegia 4","icd10cm","G11.4"
< "0110792","hereditary spastic paraplegia 4","mondo","0008438"
< "3082","interstitial lung disease","icd10cm","J84.9"
< "3082","interstitial lung disease","mesh","D017563"
< "3082","interstitial lung disease","umls","C0206062"
< "3082","interstitial lung disease","mondo","0015925"
< "10718","giardiasis","icd10cm","A07.1"
< "10718","giardiasis","icd9cm","007.1"
< "10718","giardiasis","mesh","D005873"
< "10718","giardiasis","umls","C0017536"
< "10718","giardiasis","mondo","0001103"
< "0110798","hereditary spastic paraplegia 46","icd10cm","G11.4"
< "0110798","hereditary spastic paraplegia 46","mondo","0013737"
< "2691","myoma","icd10cm","D21"
< "2691","myoma","mesh","D009214"
< "2691","myoma","umls","C0027086"
< "2691","myoma","mondo","0003061"
---
> "6212","ovarian endometrial cancer","umls","C1335159"
> "6212","ovarian endometrial cancer","umls","C1518231"
> "6212","ovarian endometrial cancer","mondo","0003812"
> "6211","mixed epithelial tumor of ovary","umls","C0346166"
> "6211","mixed epithelial tumor of ovary","mondo","0003811"
> "6210","bladder diffuse clear cell adenocarcinoma","umls","C1511187"
> "6210","bladder diffuse clear cell adenocarcinoma","mondo","0003810"
1314,1321c662,664
< "0110379","retinitis pigmentosa 43","icd10cm","H35.5"
< "0110379","retinitis pigmentosa 43","mondo","0013437"
< "0110378","retinitis pigmentosa 29","icd10cm","H35.5"
< "0110378","retinitis pigmentosa 29","mondo","0012813"
< "0110836","Usher syndrome type 1J","icd10cm","H35.5"
< "0110836","Usher syndrome type 1J","mondo","0013935"
< "0110373","retinitis pigmentosa 61","icd10cm","H35.5"
< "0110373","retinitis pigmentosa 61","mondo","0013610"
---
> "6811","juvenile pilocytic astrocytoma","mesh","D001254"
> "6811","juvenile pilocytic astrocytoma","umls","C0280783"
> "6811","juvenile pilocytic astrocytoma","mondo","0003999"
1324,1473c667,718
< "0110371","retinitis pigmentosa 56","icd10cm","H35.5"
< "0110371","retinitis pigmentosa 56","mondo","0013314"
< "0110370","retinitis pigmentosa 55","icd10cm","H35.5"
< "0110370","retinitis pigmentosa 55","mondo","0013312"
< "0110377","retinitis pigmentosa 49","icd10cm","H35.5"
< "0110377","retinitis pigmentosa 49","mondo","0013405"
< "0110376","retinitis pigmentosa 41","icd10cm","H35.5"
< "0110376","retinitis pigmentosa 41","mondo","0012796"
< "0110375","retinitis pigmentosa 40","icd10cm","H35.5"
< "0110375","retinitis pigmentosa 40","mondo","0013429"
< "0110374","retinitis pigmentosa 68","icd10cm","H35.5"
< "0110374","retinitis pigmentosa 68","mondo","0014323"
< "0110553","autosomal dominant nonsyndromic deafness 23","icd10cm","H90.3"
< "0110553","autosomal dominant nonsyndromic deafness 23","mondo","0011519"
< "14095","boutonneuse fever","icd10cm","A77.1"
< "14095","boutonneuse fever","icd9cm","082.1"
< "14095","boutonneuse fever","mesh","D001907"
< "14095","boutonneuse fever","umls","C0006060"
< "14095","boutonneuse fever","mondo","0024472"
< "0060826","syndromic X-linked intellectual disability Shashi type","icd10cm","Q87.8"
< "0060826","syndromic X-linked intellectual disability Shashi type","mondo","0010277"
< "100","intestinal infectious disease","icd10cm","A00-A09"
< "100","intestinal infectious disease","icd9cm","001-009.99"
< "100","intestinal infectious disease","umls","C0178238"
< "100","intestinal infectious disease","mondo","0000916"
< "0070264","congenital disorder of glycosylation type IIl","mondo","0013810"
< "0070265","congenital disorder of glycosylation type IIm","mondo","0010478"
< "0070266","congenital disorder of glycosylation type IIn","mondo","0014746"
< "0070267","congenital disorder of glycosylation type IIo","mondo","0014789"
< "0070260","congenital disorder of glycosylation type IIh","umls","C1970021"
< "0070260","congenital disorder of glycosylation type IIh","mondo","0012635"
< "0070261","congenital disorder of glycosylation type IIi","mondo","0013325"
< "1618","breast fibroadenoma","icd10cm","D24"
< "1618","breast fibroadenoma","mesh","D018226"
< "1618","breast fibroadenoma","umls","C0178421"
< "1618","breast fibroadenoma","umls","C0206650"
< "1618","breast fibroadenoma","umls","C0346158"
< "1618","breast fibroadenoma","umls","C1333137"
< "1618","breast fibroadenoma","mondo","0002056"
< "0070263","congenital disorder of glycosylation type IIk","mondo","0013870"
< "1964","fallopian tube cancer","icd10cm","C57.0"
< "1964","fallopian tube cancer","icd9cm","183.2"
< "1964","fallopian tube cancer","mesh","D005185"
< "1964","fallopian tube cancer","umls","C0015558"
< "1964","fallopian tube cancer","umls","C0153579"
< "1964","fallopian tube cancer","mondo","0002158"
< "1614","male breast cancer","mesh","D018567"
< "1614","male breast cancer","umls","C0242788"
< "1614","male breast cancer","mondo","0005628"
< "1967","leiomyosarcoma","mesh","D007890"
< "1967","leiomyosarcoma","umls","C0023269"
< "1967","leiomyosarcoma","mondo","0005058"
< "0070268","congenital disorder of glycosylation type IIp","mondo","0014790"
< "0070269","congenital disorder of glycosylation type IIq","mondo","0054559"
< "1963","fallopian tube carcinoma","mesh","D005185"
< "1963","fallopian tube carcinoma","umls","C0238122"
< "1963","fallopian tube carcinoma","mondo","0006206"
< "0110571","autosomal dominant nonsyndromic deafness 48","icd10cm","H90.3"
< "0110571","autosomal dominant nonsyndromic deafness 48","mondo","0011920"
< "0110570","autosomal dominant nonsyndromic deafness 47","icd10cm","H90.3"
< "0110570","autosomal dominant nonsyndromic deafness 47","mondo","0012090"
< "0110573","autosomal dominant nonsyndromic deafness 4A","icd10cm","H90.3"
< "0110573","autosomal dominant nonsyndromic deafness 4A","mondo","0010915"
< "0110572","autosomal dominant nonsyndromic deafness 49","icd10cm","H90.3"
< "0110572","autosomal dominant nonsyndromic deafness 49","mondo","0012023"
< "0110575","autosomal dominant nonsyndromic deafness 5","icd10cm","H90.3"
< "0110575","autosomal dominant nonsyndromic deafness 5","mondo","0010973"
< "0060821","syndromic X-linked intellectual disability 14","mesh","C537724"
< "0060821","syndromic X-linked intellectual disability 14","umls","C0796022"
< "0060821","syndromic X-linked intellectual disability 14","mondo","0010398"
< "0110577","autosomal dominant nonsyndromic deafness 51","icd10cm","H90.3"
< "0110577","autosomal dominant nonsyndromic deafness 51","mondo","0013305"
< "0110576","autosomal dominant nonsyndromic deafness 50","icd10cm","H90.3"
< "0110576","autosomal dominant nonsyndromic deafness 50","mondo","0013114"
< "0110579","autosomal dominant nonsyndromic deafness 53","icd10cm","H90.3"
< "0110579","autosomal dominant nonsyndromic deafness 53","mondo","0012380"
< "0110578","autosomal dominant nonsyndromic deafness 52","icd10cm","H90.3"
< "0110578","autosomal dominant nonsyndromic deafness 52","mondo","0011893"
< "13268","porphyria","icd10cm","E80.20"
< "13268","porphyria","icd9cm","277.1"
< "13268","porphyria","mesh","D011164"
< "13268","porphyria","umls","C0032708"
< "13268","porphyria","mondo","0019142"
< "0110207","Charcot-Marie-Tooth disease X-linked dominant 6","icd10cm","G60.0"
< "0110207","Charcot-Marie-Tooth disease X-linked dominant 6","mondo","0010479"
< "0110206","Charcot-Marie-Tooth disease dominant intermediate F","icd10cm","G60.0"
< "0110206","Charcot-Marie-Tooth disease dominant intermediate F","mondo","0014074"
< "0110205","Charcot-Marie-Tooth disease dominant intermediate E","icd10cm","G60.0"
< "0110205","Charcot-Marie-Tooth disease dominant intermediate E","mondo","0013758"
< "0110204","Charcot-Marie-Tooth disease recessive intermediate B","icd10cm","G60.0"
< "0110204","Charcot-Marie-Tooth disease recessive intermediate B","mondo","0013338"
< "0110203","Charcot-Marie-Tooth disease recessive intermediate D","icd10cm","G60.0"
< "0110203","Charcot-Marie-Tooth disease recessive intermediate D","mondo","0014467"
< "0110202","Charcot-Marie-Tooth disease dominant intermediate A","icd10cm","G60.0"
< "0110202","Charcot-Marie-Tooth disease dominant intermediate A","mondo","0011675"
< "0110201","Charcot-Marie-Tooth disease recessive intermediate A","mondo","0012014"
< "0110200","Charcot-Marie-Tooth disease dominant intermediate D","icd10cm","G60.0"
< "0110200","Charcot-Marie-Tooth disease dominant intermediate D","mondo","0011909"
< "0110209","Charcot-Marie-Tooth disease X-linked dominant 1","icd10cm","G60.0"
< "0110209","Charcot-Marie-Tooth disease X-linked dominant 1","mondo","0010549"
< "0110208","Charcot-Marie-Tooth disease X-linked recessive 2","icd10cm","G60.0"
< "0110208","Charcot-Marie-Tooth disease X-linked recessive 2","mondo","0010550"
< "3355","fibrosarcoma","mesh","D005354"
< "3355","fibrosarcoma","mesh","D018218"
< "3355","fibrosarcoma","umls","C0016057"
< "3355","fibrosarcoma","umls","C0206643"
< "3355","fibrosarcoma","umls","C1336021"
< "3355","fibrosarcoma","mondo","0005164"
< "3350","mesenchymal cell neoplasm","umls","C1332517"
< "3350","mesenchymal cell neoplasm","umls","C1334699"
< "3350","mesenchymal cell neoplasm","mondo","0002616"
< "14275","atrophic vulva","icd10cm","N90.5"
< "14275","atrophic vulva","icd9cm","624.1"
< "14275","atrophic vulva","umls","C0156393"
< "14275","atrophic vulva","mondo","0001932"
< "5074","malignant ependymoma","umls","C1333407"
< "5074","malignant ependymoma","mondo","0021191"
< "0060333","mitochondrial complex V (ATP synthase) deficiency nuclear type 4","icd10cm","E88.8"
< "0060333","mitochondrial complex V (ATP synthase) deficiency nuclear type 4","mondo","0014091"
< "0060332","mitochondrial complex V (ATP synthase) deficiency nuclear type 3","icd10cm","E88.8"
< "0060332","mitochondrial complex V (ATP synthase) deficiency nuclear type 3","mondo","0013547"
< "0060331","mitochondrial complex V (ATP synthase) deficiency nuclear type 2","icd10cm","G71.3"
< "0060331","mitochondrial complex V (ATP synthase) deficiency nuclear type 2","mondo","0013546"
< "0060330","Rapp-Hodgkin syndrome","mesh","C535289"
< "0060330","Rapp-Hodgkin syndrome","mondo","0007508"
< "0060337","CEDNIK syndrome","mesh","C537943"
< "0060337","CEDNIK syndrome","umls","C1836033"
< "0060337","CEDNIK syndrome","mondo","0012290"
< "0090008","immunodeficiency-centromeric instability-facial anomalies syndrome 1","icd10cm","D84.8"
< "0090008","immunodeficiency-centromeric instability-facial anomalies syndrome 1","mondo","0009454"
< "9849","Meniere's disease","icd10cm","H81.0"
< "9849","Meniere's disease","icd10cm","H81.09"
< "9849","Meniere's disease","icd9cm","386.0"
< "9849","Meniere's disease","icd9cm","386.00"
< "9849","Meniere's disease","mesh","D008575"
< "9849","Meniere's disease","umls","C0025281"
< "9849","Meniere's disease","mondo","0007972"
< "11968","postmenopausal atrophic vaginitis","icd10cm","N95.2"
< "11968","postmenopausal atrophic vaginitis","icd9cm","627.3"
< "11968","postmenopausal atrophic vaginitis","umls","C0156409"
< "11968","postmenopausal atrophic vaginitis","mondo","0001410"
< "0060339","chronic atrial and intestinal dysrhythmia","mondo","0014528"
< "2544","extratemporal epilepsy","umls","C0270849"
< "2544","extratemporal epilepsy","mondo","0002338"
< "5446","eccrine papillary adenoma","umls","C0334350"
< "5446","eccrine papillary adenoma","mondo","0003450"
< "0110223","Brugada syndrome 6","icd10cm","I49.8"
< "0110223","Brugada syndrome 6","mondo","0013145"
< "0090006","renal coloboma syndrome","icd10cm","Q60.4"
< "0090006","renal coloboma syndrome","mondo","0007352"
---
> "6812","childhood pilocytic astrocytoma","umls","C1332995"
> "6812","childhood pilocytic astrocytoma","mondo","0004000"
> "10516","malignant otitis externa","icd10cm","H60.2"
> "10516","malignant otitis externa","icd10cm","H60.20"
> "10516","malignant otitis externa","icd9cm","380.14"
> "10516","malignant otitis externa","umls","C0155395"
> "10516","malignant otitis externa","mondo","0001050"
> "0110448","dilated cardiomyopathy 1HH","icd10cm","I42.0"
> "0110448","dilated cardiomyopathy 1HH","mondo","0013479"
> "0110838","Usher syndrome type 2A","icd10cm","H35.5"
> "0110838","Usher syndrome type 2A","mondo","0010169"
> "9754","ganglion or cyst of synovium/tendon/bursa","icd9cm","727.49"
> "9754","ganglion or cyst of synovium/tendon/bursa","umls","C0158336"
> "9754","ganglion or cyst of synovium/tendon/bursa","mondo","0004874"
> "10579","leukodystrophy","icd9cm","330.0"
> "10579","leukodystrophy","umls","C0023520"
> "10579","leukodystrophy","mondo","0019046"
> "0110839","Usher syndrome type 2C","icd10cm","H35.5"
> "0110839","Usher syndrome type 2C","mondo","0011558"
> "10575","calcium metabolism disease","icd10cm","E83.5"
> "10575","calcium metabolism disease","icd10cm","E83.50"
> "10575","calcium metabolism disease","icd9cm","275.4"
> "10575","calcium metabolism disease","icd9cm","275.40"
> "10575","calcium metabolism disease","mesh","D002128"
> "10575","calcium metabolism disease","umls","C0006705"
> "10575","calcium metabolism disease","mondo","0005557"
> "10573","osteomalacia","icd9cm","268.2"
> "10573","osteomalacia","mesh","D010018"
> "10573","osteomalacia","umls","C0029442"
> "10573","osteomalacia","mondo","0001068"
> "13548","secondary Parkinson disease","icd10cm","G21"
> "13548","secondary Parkinson disease","icd10cm","G21.9"
> "13548","secondary Parkinson disease","icd9cm","332.1"
> "13548","secondary Parkinson disease","mesh","D010302"
> "13548","secondary Parkinson disease","umls","C0030569"
> "13548","secondary Parkinson disease","mondo","0006966"
> "13549","interval angle-closure glaucoma","icd10cm","H40.23"
> "13549","interval angle-closure glaucoma","icd9cm","365.21"
> "13549","interval angle-closure glaucoma","umls","C0154945"
> "13549","interval angle-closure glaucoma","mondo","0001742"
> "8849","sublingual gland cancer","icd10cm","C08.1"
> "8849","sublingual gland cancer","icd9cm","142.2"
> "8849","sublingual gland cancer","umls","C0153361"
> "8849","sublingual gland cancer","mondo","0004667"
> "14400","capillary leak syndrome","mesh","D019559"
> "14400","capillary leak syndrome","umls","C0343084"
> "14400","capillary leak syndrome","mondo","0001956"
> "0111265","Boucher-Neuhauser syndrome","umls","C1859093"
> "7665","non-gestational ovarian choriocarcinoma","umls","C1518355"
> "7665","non-gestational ovarian choriocarcinoma","mondo","0004322"
> "7664","endometrial mixed adenocarcinoma","umls","C1516856"
> "7664","endometrial mixed adenocarcinoma","mondo","0004321"
1479c724,737
< "0111119","nephronophthisis 12","mondo","0013442"
---
> "0040083","Chlamydia pneumonia","icd10cm","J16.0"
> "0040083","Chlamydia pneumonia","icd9cm","483.1"
> "0040083","Chlamydia pneumonia","mondo","0025598"
> "14402","critical illness polyneuropathy","icd10cm","G62.81"
> "14402","critical illness polyneuropathy","icd9cm","357.82"
> "14402","critical illness polyneuropathy","mesh","D011115"
> "14402","critical illness polyneuropathy","umls","C0393851"
> "14402","critical illness polyneuropathy","mondo","0001957"
> "1760","facial nerve neoplasm","umls","C1263899"
> "1760","facial nerve neoplasm","mondo","0002101"
> "1761","Melkersson-Rosenthal syndrome","icd10cm","G51.2"
> "1761","Melkersson-Rosenthal syndrome","mesh","D008556"
> "1761","Melkersson-Rosenthal syndrome","umls","C0025235"
> "1761","Melkersson-Rosenthal syndrome","mondo","0007969"
1484,1521c742,748
< "0040086","Polyomavirus-associated Nephropathy","umls","C1697878"
< "0040086","Polyomavirus-associated Nephropathy","mondo","0022529"
< "6961","Bartholin's gland squamous cell carcinoma","umls","C1511052"
< "6961","Bartholin's gland squamous cell carcinoma","mondo","0004053"
< "0090005","Schwartz-Jampel syndrome 1","icd10cm","G71.1"
< "0090005","Schwartz-Jampel syndrome 1","mondo","0009717"
< "8158","complement component 5 deficiency","mondo","0012295"
< "6969","acute canaliculitis","icd10cm","H04.33"
< "6969","acute canaliculitis","icd9cm","375.31"
< "6969","acute canaliculitis","umls","C0339130"
< "6969","acute canaliculitis","mondo","0004054"
< "5621","histiocytic and dendritic cell cancer","umls","C1334030"
< "5621","histiocytic and dendritic cell cancer","mondo","0006247"
< "11193","syndactyly","icd10cm","Q70"
< "11193","syndactyly","icd10cm","Q70.9"
< "11193","syndactyly","icd9cm","755.1"
< "11193","syndactyly","mesh","D013576"
< "11193","syndactyly","umls","C0039075"
< "11193","syndactyly","mondo","0021002"
< "8622","measles","icd10cm","B05"
< "8622","measles","icd10cm","B05.9"
< "8622","measles","icd9cm","055"
< "8622","measles","mesh","D008457"
< "8622","measles","umls","C0025007"
< "8622","measles","mondo","0004619"
< "5508","brain stem ependymoma","umls","C1332609"
< "5508","brain stem ependymoma","mondo","0003477"
< "5502","lice infestation","icd10cm","B85.2"
< "5502","lice infestation","icd9cm","132.9"
< "5502","lice infestation","mesh","D010373"
< "5502","lice infestation","umls","C0030756"
< "5502","lice infestation","mondo","0003472"
< "5503","spinal cord ependymoma","umls","C0238432"
< "5503","spinal cord ependymoma","mondo","0003473"
< "5501","Pediculus humanus capitis infestation","icd10cm","B85.0"
< "5501","Pediculus humanus capitis infestation","icd9cm","132.0"
< "5501","Pediculus humanus capitis infestation","umls","C0030757"
< "5501","Pediculus humanus capitis infestation","mondo","0003471"
---
> "0040086","Polyomavirus-associated nephropathy","umls","C1697878"
> "0040086","Polyomavirus-associated nephropathy","mondo","0022529"
> "0040085","bacterial sepsis","icd9cm","995.91"
> "0040085","bacterial sepsis","mondo","0005229"
> "0040084","Streptococcus pneumonia","icd10cm","J13"
> "0040084","Streptococcus pneumonia","icd9cm","481"
> "0040084","Streptococcus pneumonia","mondo","0005972"
1526a754,756
> "693","dental enamel hypoplasia","mesh","D003744"
> "693","dental enamel hypoplasia","umls","C0011351"
> "693","dental enamel hypoplasia","mondo","0004038"
1536,1567c766,792
< "0111126","nephronophthisis 19","mondo","0014537"
< "0060485","Mowat-Wilson syndrome","mesh","C536990"
< "0060485","Mowat-Wilson syndrome","umls","C1856113"
< "0060485","Mowat-Wilson syndrome","mondo","0009341"
< "0060484","EAST syndrome","mesh","C557674"
< "0060484","EAST syndrome","umls","C2748572"
< "0060484","EAST syndrome","mondo","0013005"
< "0060486","Perry syndrome","mesh","C566822"
< "0060486","Perry syndrome","mondo","0008201"
< "0060481","Goldberg-Shprintzen syndrome","mesh","C537279"
< "0060481","Goldberg-Shprintzen syndrome","umls","C1836123"
< "0060481","Goldberg-Shprintzen syndrome","mondo","0012280"
< "0060480","left ventricular noncompaction","mondo","0018901"
< "0060483","MEDNIK syndrome","mondo","0012251"
< "11235","adhesive otitis media","icd10cm","H74.1"
< "11235","adhesive otitis media","icd9cm","385.1"
< "11235","adhesive otitis media","icd9cm","385.10"
< "11235","adhesive otitis media","umls","C0155478"
< "11235","adhesive otitis media","mondo","0001234"
< "2846","bruxism","icd10cm","F45.8"
< "2846","bruxism","icd10cm","G47.63"
< "2846","bruxism","icd9cm","327.53"
< "2846","bruxism","mesh","D002012"
< "2846","bruxism","mesh","D020186"
< "2846","bruxism","umls","C0006325"
< "2846","bruxism","umls","C0393774"
< "2846","bruxism","mondo","0002443"
< "2382","kernicterus","icd10cm","P57"
< "2382","kernicterus","icd10cm","P57.9"
< "2382","kernicterus","mesh","D007647"
< "2382","kernicterus","umls","C0022610"
< "2382","kernicterus","mondo","0006819"
---
> "11111","hydronephrosis","icd10cm","N13.30"
> "11111","hydronephrosis","icd9cm","591"
> "11111","hydronephrosis","mesh","D006869"
> "11111","hydronephrosis","umls","C0020295"
> "11111","hydronephrosis","mondo","0005510"
> "698","dentin sensitivity","mesh","D003807"
> "698","dentin sensitivity","umls","C0011432"
> "698","dentin sensitivity","mondo","0004059"
> "699","mitochondrial myopathy","mesh","D017240"
> "699","mitochondrial myopathy","umls","C0162670"
> "699","mitochondrial myopathy","mondo","0009637"
> "8712","neurofibromatosis","icd10cm","Q85.00"
> "8712","neurofibromatosis","icd10cm","Q85.01"
> "8712","neurofibromatosis","icd10cm","Q85.02"
> "8712","neurofibromatosis","icd9cm","237.7"
> "8712","neurofibromatosis","icd9cm","237.70"
> "8712","neurofibromatosis","icd9cm","237.71"
> "8712","neurofibromatosis","icd9cm","237.72"
> "8712","neurofibromatosis","mesh","C537392"
> "8712","neurofibromatosis","mesh","D009456"
> "8712","neurofibromatosis","mesh","D016518"
> "8712","neurofibromatosis","mesh","D017253"
> "8712","neurofibromatosis","umls","C0027831"
> "8712","neurofibromatosis","umls","C0027832"
> "8712","neurofibromatosis","umls","C0162678"
> "8712","neurofibromatosis","umls","C0220695"
> "8712","neurofibromatosis","mondo","0021061"
1575,1598c800,809
< "0060246","MASA syndrome","mesh","C536029"
< "0060246","MASA syndrome","umls","C0795953"
< "0060246","MASA syndrome","mondo","0010559"
< "0060245","Mast syndrome","icd10cm","G11.4"
< "0060245","Mast syndrome","mesh","C565409"
< "0060245","Mast syndrome","mondo","0009568"
< "0060243","stuttering","icd10cm","F80.81"
< "0060243","stuttering","mesh","D013342"
< "0060243","stuttering","umls","C0038131"
< "0060243","stuttering","umls","C0038506"
< "0060243","stuttering","umls","C0454542"
< "0060243","stuttering","umls","C0751527"
< "0060243","stuttering","umls","C0751528"
< "0060243","stuttering","umls","C0751529"
< "0060243","stuttering","umls","C3489627"
< "0060243","stuttering","mondo","0000723"
< "0060242","synpolydactyly","mesh","C538153"
< "0060242","synpolydactyly","umls","C2699746"
< "0060242","synpolydactyly","mondo","0000722"
< "0060241","3-M syndrome","mesh","C535314"
< "0060241","3-M syndrome","mesh","C535725"
< "0060241","3-M syndrome","umls","C1848862"
< "0060241","3-M syndrome","umls","C1851996"
< "0060241","3-M syndrome","mondo","0007477"
---
> "8719","in situ carcinoma","icd10cm","D09.9"
> "8719","in situ carcinoma","icd9cm","230-234.99"
> "8719","in situ carcinoma","icd9cm","234.9"
> "8719","in situ carcinoma","mesh","D002278"
> "8719","in situ carcinoma","umls","C0007099"
> "8719","in situ carcinoma","mondo","0004647"
> "0060467","humeroradial synostosis","icd10cm","Q74.0"
> "0060467","humeroradial synostosis","mesh","C535284"
> "0060467","humeroradial synostosis","umls","C0431800"
> "0060467","humeroradial synostosis","mondo","0007737"
1601a813,815
> "0060465","fibrochondrogenesis","mesh","C562524"
> "0060465","fibrochondrogenesis","umls","C0265282"
> "0060465","fibrochondrogenesis","mondo","0016068"
1610,1614c824,827
< "341","peripheral vascular disease","icd9cm","443.81"
< "341","peripheral vascular disease","mesh","D016491"
< "341","peripheral vascular disease","umls","C0003838"
< "341","peripheral vascular disease","umls","C0031115"
< "341","peripheral vascular disease","mondo","0005294"
---
> "0060461","chromosome Xp11.23-p11.22 duplication syndrome","icd10cm","Q99.8"
> "0060461","chromosome Xp11.23-p11.22 duplication syndrome","mondo","0010428"
> "0060460","chromosome 5p13 duplication syndrome","icd10cm","Q92.3"
> "0060460","chromosome 5p13 duplication syndrome","mondo","0013169"
1619,1661c832,835
< "0110219","Brugada syndrome 2","icd10cm","I49.8"
< "0110219","Brugada syndrome 2","mondo","0012728"
< "9988","tertiary neurosyphilis","icd10cm","A52.3"
< "9988","tertiary neurosyphilis","icd9cm","094"
< "9988","tertiary neurosyphilis","icd9cm","094.9"
< "9988","tertiary neurosyphilis","mesh","D009494"
< "9988","tertiary neurosyphilis","umls","C0027927"
< "9988","tertiary neurosyphilis","mondo","0004944"
< "7880","luteoma","mesh","D018311"
< "7880","luteoma","umls","C1517842"
< "7880","luteoma","mondo","0004387"
< "8023","myxoid liposarcoma of the ovary","umls","C1335170"
< "8023","myxoid liposarcoma of the ovary","mondo","0004436"
< "8533","hypopharynx cancer","icd10cm","C13"
< "8533","hypopharynx cancer","icd10cm","C13.2"
< "8533","hypopharynx cancer","icd10cm","C13.9"
< "8533","hypopharynx cancer","icd9cm","148"
< "8533","hypopharynx cancer","icd9cm","148.3"
< "8533","hypopharynx cancer","icd9cm","148.9"
< "8533","hypopharynx cancer","mesh","D007012"
< "8533","hypopharynx cancer","umls","C0153398"
< "8533","hypopharynx cancer","umls","C0496770"
< "8533","hypopharynx cancer","mondo","0005806"
< "11760","Kohler's disease","icd9cm","732.5"
< "11760","Kohler's disease","umls","C0158444"
< "11760","Kohler's disease","mondo","0016086"
< "8536","herpes zoster","icd10cm","B02"
< "8536","herpes zoster","icd10cm","B02.9"
< "8536","herpes zoster","icd9cm","053"
< "8536","herpes zoster","mesh","D006562"
< "8536","herpes zoster","umls","C0019360"
< "8536","herpes zoster","mondo","0005609"
< "14504","Niemann-Pick disease","icd10cm","E75.24"
< "14504","Niemann-Pick disease","icd10cm","E75.249"
< "14504","Niemann-Pick disease","mesh","D009542"
< "14504","Niemann-Pick disease","umls","C0028064"
< "14504","Niemann-Pick disease","mondo","0001982"
< "7442","monoclonal gammopathy of uncertain significance","mondo","0004225"
< "3321","GM2 gangliosidosis","icd10cm","E75.0"
< "3321","GM2 gangliosidosis","icd10cm","E75.00"
< "3321","GM2 gangliosidosis","mesh","D020143"
< "3321","GM2 gangliosidosis","umls","C0268274"
< "3321","GM2 gangliosidosis","mondo","0017720"
---
> "0060468","Holt-Oram syndrome","icd10cm","Q87.2"
> "0060468","Holt-Oram syndrome","mesh","C535326"
> "0060468","Holt-Oram syndrome","umls","C0265264"
> "0060468","Holt-Oram syndrome","mondo","0007732"
1670,1716c844,857
< "12474","capillariasis","icd10cm","B81.1"
< "12474","capillariasis","icd9cm","127.5"
< "12474","capillariasis","mesh","D017189"
< "12474","capillariasis","umls","C0006897"
< "12474","capillariasis","mondo","0001532"
< "0060799","syndromic X-linked intellectual disability Lubs type","mesh","C537723"
< "0060799","syndromic X-linked intellectual disability Lubs type","umls","C1846058"
< "0060799","syndromic X-linked intellectual disability Lubs type","mondo","0010283"
< "0060798","hypomyelinating leukodystrophy 6","icd10cm","E75.2"
< "0060798","hypomyelinating leukodystrophy 6","mondo","0012905"
< "14179","Bruton-type agammaglobulinemia","mesh","C537409"
< "14179","Bruton-type agammaglobulinemia","umls","C0221026"
< "14179","Bruton-type agammaglobulinemia","mondo","0010421"
< "0060791","hypomyelinating leukodystrophy 9","icd10cm","E75.2"
< "0060791","hypomyelinating leukodystrophy 9","mondo","0014506"
< "0060790","hypomyelinating leukodystrophy 3","icd10cm","E75.2"
< "0060790","hypomyelinating leukodystrophy 3","mondo","0009843"
< "0060061","cutaneous T cell lymphoma","mesh","D016410"
< "0060061","cutaneous T cell lymphoma","mondo","0000607"
< "0060792","hypomyelinating leukodystrophy 11","icd10cm","G11.1"
< "0060792","hypomyelinating leukodystrophy 11","mondo","0014666"
< "1380","endometrial cancer","kegg","05213"
< "1380","endometrial cancer","icd10cm","C54.1"
< "1380","endometrial cancer","mesh","D016889"
< "1380","endometrial cancer","umls","C0007103"
< "1380","endometrial cancer","umls","C0014170"
< "1380","endometrial cancer","mondo","0011962"
< "0060794","hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism","icd10cm","G11.1"
< "0060794","hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism","mondo","0011897"
< "0060797","hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism","icd10cm","G11.1"
< "0060797","hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism","mondo","0013722"
< "0060796","hypomyelinating leukodystrophy 12","mondo","0014732"
< "3827","congenital diaphragmatic hernia","icd10cm","K44"
< "3827","congenital diaphragmatic hernia","icd10cm","K44.9"
< "3827","congenital diaphragmatic hernia","mesh","D006548"
< "3827","congenital diaphragmatic hernia","umls","C0019284"
< "3827","congenital diaphragmatic hernia","mondo","0005711"
< "9155","mucocutaneous leishmaniasis","icd10cm","B55.2"
< "9155","mucocutaneous leishmaniasis","icd9cm","085.5"
< "9155","mucocutaneous leishmaniasis","mesh","D007897"
< "9155","mucocutaneous leishmaniasis","umls","C1328252"
< "9155","mucocutaneous leishmaniasis","mondo","0005859"
< "5713","mediastinum liposarcoma","umls","C1334663"
< "5713","mediastinum liposarcoma","mondo","0003601"
< "3829","pituitary adenoma","mesh","D010911"
< "3829","pituitary adenoma","umls","C0032000"
< "3829","pituitary adenoma","mondo","0006373"
---
> "5614","eye disease","icd10cm","H44"
> "5614","eye disease","icd10cm","H44.9"
> "5614","eye disease","icd9cm","360"
> "5614","eye disease","icd9cm","360.9"
> "5614","eye disease","icd9cm","379.90"
> "5614","eye disease","mesh","D005128"
> "5614","eye disease","umls","C0015397"
> "5614","eye disease","mondo","0005328"
> "5615","spinal canal intradural extramedullary neoplasm","umls","C1334255"
> "5615","spinal canal intradural extramedullary neoplasm","mondo","0003545"
> "12363","intermittent proptosis","icd10cm","H05.25"
> "12363","intermittent proptosis","icd9cm","376.34"
> "12363","intermittent proptosis","umls","C0155270"
> "12363","intermittent proptosis","mondo","0001512"
1721,1723c862,866
< "8443","brachial plexus lesion","icd9cm","353.0"
< "8443","brachial plexus lesion","umls","C0006091"
< "8443","brachial plexus lesion","mondo","0004569"
---
> "11561","hypertensive retinopathy","icd10cm","H35.03"
> "11561","hypertensive retinopathy","icd9cm","362.11"
> "11561","hypertensive retinopathy","mesh","D058437"
> "11561","hypertensive retinopathy","umls","C0152132"
> "11561","hypertensive retinopathy","mondo","0006797"
1729,1786c872,873
< "0070298","multiple epiphyseal dysplasia 2","mondo","0010844"
< "4283","anal margin basal cell carcinoma","icd10cm","C44.510"
< "4283","anal margin basal cell carcinoma","umls","C1332269"
< "4283","anal margin basal cell carcinoma","mondo","0002940"
< "4280","nodular basal cell carcinoma","umls","C1304300"
< "4280","nodular basal cell carcinoma","mondo","0002937"
< "4284","anal margin carcinoma","umls","C0349534"
< "4284","anal margin carcinoma","mondo","0002941"
< "13994","cleidocranial dysplasia","icd10cm","Q74.0"
< "13994","cleidocranial dysplasia","mesh","D002973"
< "13994","cleidocranial dysplasia","umls","C0008928"
< "13994","cleidocranial dysplasia","mondo","0007340"
< "4288","external ear carcinoma","umls","C1333492"
< "4288","external ear carcinoma","mondo","0002944"
< "0060025","immunoglobulin alpha deficiency","mesh","D017098"
< "0060025","immunoglobulin alpha deficiency","umls","C0162538"
< "0060025","immunoglobulin alpha deficiency","mondo","0001341"
< "11360","Phlebotomus fever","icd10cm","A93.1"
< "11360","Phlebotomus fever","icd9cm","066.0"
< "11360","Phlebotomus fever","mesh","D010217"
< "11360","Phlebotomus fever","umls","C0030372"
< "11360","Phlebotomus fever","mondo","0005913"
< "0060067","Pearson syndrome","mondo","0010797"
< "1176","bronchial disease","mesh","D001982"
< "1176","bronchial disease","umls","C0006261"
< "1176","bronchial disease","mondo","0001358"
< "7539","pregnancy adenoma","umls","C1266023"
< "7539","pregnancy adenoma","mondo","0004271"
< "368","cerebrum cancer","icd9cm","191.8"
< "368","cerebrum cancer","umls","C0153642"
< "368","cerebrum cancer","umls","C1263885"
< "368","cerebrum cancer","mondo","0002731"
< "5134","anus leiomyoma","umls","C1332266"
< "5134","anus leiomyoma","mondo","0003292"
< "0060023","CD40 deficiency","mondo","0011735"
< "365","bladder disease","icd10cm","N32.9"
< "365","bladder disease","icd9cm","596.9"
< "365","bladder disease","mesh","D001745"
< "365","bladder disease","umls","C0005686"
< "365","bladder disease","mondo","0006026"
< "7531","anal gland adenocarcinoma","umls","C1266027"
< "7531","anal gland adenocarcinoma","mondo","0004266"
< "363","uterine cancer","icd10cm","C55"
< "363","uterine cancer","icd9cm","179"
< "363","uterine cancer","mesh","D014594"
< "363","uterine cancer","umls","C0042138"
< "363","uterine cancer","umls","C0153567"
< "363","uterine cancer","mondo","0002715"
< "0060022","CD40 ligand deficiency","mondo","0010626"
< "9255","frontotemporal dementia","mesh","C563003"
< "9255","frontotemporal dementia","mesh","D057180"
< "9255","frontotemporal dementia","umls","C0520716"
< "9255","frontotemporal dementia","mondo","0017276"
< "5605","breast medullary carcinoma","umls","C0860580"
< "5605","breast medullary carcinoma","mondo","0005063"
< "0060753","familial temporal lobe epilepsy 4","mondo","0012706"
< "5275","gallbladder leiomyosarcoma","umls","C1333746"
< "5275","gallbladder leiomyosarcoma","mondo","0003364"
---
> "0070295","primary autosomal dominant microcephaly 18","mondo","0054593"
> "0070296","primary autosomal recessive microcephaly","mondo","0016660"
1788,1790c875,878
< "0060752","familial temporal lobe epilepsy 5","mondo","0013741"
< "2766","ethmoid sinus adenocarcinoma","umls","C1333472"
< "2766","ethmoid sinus adenocarcinoma","mondo","0002418"
---
> "9521","Laron syndrome","icd10cm","E34.3"
> "9521","Laron syndrome","mesh","D046150"
> "9521","Laron syndrome","umls","C0271568"
> "9521","Laron syndrome","mondo","0009877"
1793,1805c881
< "381","arthropathy","icd10cm","M00-M02"
< "381","arthropathy","icd10cm","M12.9"
< "381","arthropathy","icd10cm","M19.90"
< "381","arthropathy","icd10cm","M25.9"
< "381","arthropathy","icd9cm","711"
< "381","arthropathy","icd9cm","716.9"
< "381","arthropathy","icd9cm","716.90"
< "381","arthropathy","icd9cm","719.9"
< "381","arthropathy","icd9cm","719.90"
< "381","arthropathy","mesh","D007592"
< "381","arthropathy","umls","C0022408"
< "381","arthropathy","umls","C0157749"
< "381","arthropathy","mondo","0006816"
---
> "0110974","brachydactyly type A1B","mondo","0011757"
1809c885,887
< "0070293","primary autosomal recessive microcephaly 2 with or without cortical malformations","mondo","0011435"
---
> "9250","acrocallosal syndrome","mesh","D055673"
> "9250","acrocallosal syndrome","umls","C0796147"
> "9250","acrocallosal syndrome","mondo","0008708"
1814,1825d891
< "367","olfactory nerve disease","icd10cm","G52.0"
< "367","olfactory nerve disease","icd9cm","352.0"
< "367","olfactory nerve disease","mesh","D020431"
< "367","olfactory nerve disease","umls","C0751937"
< "367","olfactory nerve disease","mondo","0002727"
< "115","cardiac tamponade","icd10cm","I31.4"
< "115","cardiac tamponade","icd9cm","423.3"
< "115","cardiac tamponade","mesh","D002305"
< "115","cardiac tamponade","umls","C0007177"
< "115","cardiac tamponade","mondo","0001297"
< "0070119","Meckel syndrome 5","icd10cm","Q61.9"
< "0070119","Meckel syndrome 5","mondo","0012695"
1828,1831d893
< "12721","multiple epiphyseal dysplasia","icd9cm","756.56"
< "12721","multiple epiphyseal dysplasia","mesh","D010009"
< "12721","multiple epiphyseal dysplasia","umls","C0026760"
< "12721","multiple epiphyseal dysplasia","mondo","0016648"
1838,1842c900,909
< "10983","Alport syndrome","mesh","D009394"
< "10983","Alport syndrome","umls","C0027706"
< "10983","Alport syndrome","mondo","0018965"
< "0060758","immunodeficiency with hyper-IgM type 2","icd10cm","D80.5"
< "0060758","immunodeficiency with hyper-IgM type 2","mondo","0011528"
---
> "10254","strawberry gallbladder","icd10cm","K82.4"
> "10254","strawberry gallbladder","icd9cm","575.6"
> "10254","strawberry gallbladder","umls","C0152456"
> "10254","strawberry gallbladder","mondo","0000987"
> "6774","polyembryoma of the ovary","umls","C1514199"
> "6774","polyembryoma of the ovary","mondo","0003989"
> "6776","breast myoepithelial carcinoma","umls","C1518167"
> "6776","breast myoepithelial carcinoma","mondo","0003990"
> "6777","villoglandular endometrial endometrioid adenocarcinoma","umls","C1336962"
> "6777","villoglandular endometrial endometrioid adenocarcinoma","mondo","0003991"
1850,1879c917,920
< "5870","eosinophilic pneumonia","icd10cm","J82"
< "5870","eosinophilic pneumonia","mesh","D011657"
< "5870","eosinophilic pneumonia","umls","C1527407"
< "5870","eosinophilic pneumonia","mondo","0005749"
< "5875","retroperitoneal cancer","icd10cm","C48"
< "5875","retroperitoneal cancer","icd10cm","C48.0"
< "5875","retroperitoneal cancer","icd9cm","158"
< "5875","retroperitoneal cancer","icd9cm","158.0"
< "5875","retroperitoneal cancer","mesh","D012186"
< "5875","retroperitoneal cancer","umls","C0035358"
< "5875","retroperitoneal cancer","umls","C0153464"
< "5875","retroperitoneal cancer","umls","C0153465"
< "5875","retroperitoneal cancer","mondo","0005941"
< "11294","arteriovenous malformation","icd10cm","I77.0"
< "11294","arteriovenous malformation","umls","C0334533"
< "11294","arteriovenous malformation","mondo","0001256"
< "0050723","PSAT deficiency","mondo","0012596"
< "0050722","PHGDH deficiency","mesh","C566618"
< "0050722","PHGDH deficiency","mondo","0011152"
< "0050720","ornithine translocase deficiency","mondo","0009393"
< "0050726","tyrosinemia type I","mondo","0010161"
< "0050725","tyrosinemia type II","mondo","0010160"
< "0050724","PSPH deficiency","mondo","0013531"
< "3750","urethra squamous cell carcinoma","umls","C1336890"
< "3750","urethra squamous cell carcinoma","mondo","0002764"
< "0050729","neutral lipid storage disease","mondo","0015611"
< "3755","antithrombin III deficiency","icd10cm","D68.59"
< "3755","antithrombin III deficiency","mesh","D020152"
< "3755","antithrombin III deficiency","umls","C0272375"
< "3755","antithrombin III deficiency","mondo","0013144"
---
> "9969","carotenemia","icd10cm","E67.1"
> "9969","carotenemia","icd9cm","278.3"
> "9969","carotenemia","umls","C0154271"
> "9969","carotenemia","mondo","0004935"
1888,1899c929,934
< "1070","primary open angle glaucoma","icd10cm","H40.11"
< "1070","primary open angle glaucoma","icd9cm","365.11"
< "1070","primary open angle glaucoma","mesh","D005902"
< "1070","primary open angle glaucoma","umls","C0339573"
< "1070","primary open angle glaucoma","mondo","0007665"
< "0080139","multiple congenital anomalies-hypotonia-seizures syndrome 2","mondo","0010466"
< "252","alcoholic psychosis","icd9cm","291.9"
< "252","alcoholic psychosis","mesh","D011604"
< "252","alcoholic psychosis","umls","C0033936"
< "252","alcoholic psychosis","mondo","0002330"
< "0110813","hereditary spastic paraplegia 62","icd10cm","G11.4"
< "0110813","hereditary spastic paraplegia 62","mondo","0014302"
---
> "0060801","MEHMO syndrome","mesh","C537451"
> "0060801","MEHMO syndrome","umls","C1846278"
> "0060801","MEHMO syndrome","mondo","0010258"
> "0060800","syndromic X-linked intellectual disability 5","mesh","C535773"
> "0060800","syndromic X-linked intellectual disability 5","umls","C0796254"
> "0060800","syndromic X-linked intellectual disability 5","mondo","0010574"
1906,1955c941,954
< "0110814","hereditary spastic paraplegia 63","icd10cm","G11.4"
< "0110814","hereditary spastic paraplegia 63","mondo","0014305"
< "0060806","syndromic X-linked intellectual disability Hedera type","mondo","0010319"
< "0111033","African iron overload","icd10cm","E83.1"
< "0111033","African iron overload","mondo","0011012"
< "0111032","hemochromatosis type 2B","mondo","0013220"
< "0111031","hemochromatosis type 5","icd10cm","E83.1"
< "0111031","hemochromatosis type 5","mondo","0014225"
< "0111030","hemochromatosis type 3","mesh","C537248"
< "0111030","hemochromatosis type 3","umls","C1858664"
< "0111030","hemochromatosis type 3","mondo","0011417"
< "0111037","glycine N-methyltransferase deficiency","icd10cm","E72.1"
< "0111037","glycine N-methyltransferase deficiency","mondo","0011698"
< "0111036","CADASIL 2","icd10cm","F01.1"
< "0111036","CADASIL 2","mondo","0014768"
< "0111035","CADASIL 1","icd10cm","F01.1"
< "0111035","CADASIL 1","mondo","0000914"
< "0111034","hemochromatosis type 2","icd10cm","E83.1"
< "0111034","hemochromatosis type 2","mesh","C537247"
< "0111034","hemochromatosis type 2","mondo","0019257"
< "11748","round ligament malignant neoplasm","icd10cm","C57.2"
< "11748","round ligament malignant neoplasm","icd9cm","183.5"
< "11748","round ligament malignant neoplasm","umls","C0346867"
< "11748","round ligament malignant neoplasm","mondo","0001352"
< "0070053","autosomal dominant non-syndromic intellectual disability 23","mondo","0014336"
< "0111039","hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase","icd10cm","E72.1"
< "0111039","hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase","mondo","0013404"
< "0111038","hypermethioninemia due to adenosine kinase deficiency","icd10cm","E72.1"
< "0111038","hypermethioninemia due to adenosine kinase deficiency","mondo","0013676"
< "6688","autoimmune lymphoproliferative syndrome","icd10cm","D89.82"
< "6688","autoimmune lymphoproliferative syndrome","icd9cm","279.41"
< "6688","autoimmune lymphoproliferative syndrome","mesh","D056735"
< "6688","autoimmune lymphoproliferative syndrome","umls","C1328840"
< "6688","autoimmune lymphoproliferative syndrome","mondo","0017979"
< "6680","Capgras syndrome","mesh","D002194"
< "6680","Capgras syndrome","umls","C0006895"
< "6680","Capgras syndrome","mondo","0003965"
< "6683","Aarskog syndrome","icd10cm","Q87.1"
< "6683","Aarskog syndrome","mesh","C535331"
< "6683","Aarskog syndrome","umls","C0175701"
< "6683","Aarskog syndrome","mondo","0007030"
< "0110885","inflammatory bowel disease 10","mondo","0012610"
< "906","peroxisomal disease","icd10cm","E71.5"
< "906","peroxisomal disease","icd10cm","E71.50"
< "906","peroxisomal disease","icd9cm","277.86"
< "906","peroxisomal disease","mesh","D018901"
< "906","peroxisomal disease","umls","C0282528"
< "906","peroxisomal disease","mondo","0019053"
< "0110732","neuronal ceroid lipofuscinosis 11","icd10cm","E75.4"
< "0110732","neuronal ceroid lipofuscinosis 11","mondo","0013866"
---
> "0060807","syndromic X-linked intellectual disability Najm type","icd10cm","Q04.3"
> "0060807","syndromic X-linked intellectual disability Najm type","mondo","0010417"
> "255","hemangioma","icd10cm","D18.0"
> "255","hemangioma","icd10cm","D18.00"
> "255","hemangioma","icd9cm","228.0"
> "255","hemangioma","icd9cm","228.00"
> "255","hemangioma","mesh","D006391"
> "255","hemangioma","umls","C0018916"
> "255","hemangioma","mondo","0006500"
> "12030","panuveitis","icd10cm","H44.11"
> "12030","panuveitis","icd9cm","360.12"
> "12030","panuveitis","mesh","D015864"
> "12030","panuveitis","umls","C0030343"
> "12030","panuveitis","mondo","0017255"
1961a961,966
> "9500","leukocyte disease","icd10cm","D72.9"
> "9500","leukocyte disease","icd9cm","288"
> "9500","leukocyte disease","icd9cm","288.9"
> "9500","leukocyte disease","mesh","D007960"
> "9500","leukocyte disease","umls","C0023510"
> "9500","leukocyte disease","mondo","0004805"
1967,1968c972,978
< "0110731","neuronal ceroid lipofuscinosis 3","icd10cm","E75.4"
< "0110731","neuronal ceroid lipofuscinosis 3","mondo","0008767"
---
> "9507","ethmoid sinusitis","icd10cm","J32.2"
> "9507","ethmoid sinusitis","mesh","D015521"
> "9507","ethmoid sinusitis","umls","C0015029"
> "9507","ethmoid sinusitis","mondo","0005756"
> "9504","benign mammary dysplasia","icd9cm","610.8"
> "9504","benign mammary dysplasia","umls","C0156319"
> "9504","benign mammary dysplasia","mondo","0004808"
1975,1985c985,988
< "0070079","schizophrenia 3","mondo","0010897"
< "0070078","schizophrenia 2","mondo","0011307"
< "0110886","inflammatory bowel disease 9","mondo","0012040"
< "7849","dendritic cell sarcoma","umls","C1301364"
< "7849","dendritic cell sarcoma","mondo","0004380"
< "169","neuroendocrine tumor","icd10cm","D3A.8"
< "169","neuroendocrine tumor","icd9cm","209"
< "169","neuroendocrine tumor","icd9cm","209-209.99"
< "169","neuroendocrine tumor","mesh","D018358"
< "169","neuroendocrine tumor","umls","C0206754"
< "169","neuroendocrine tumor","mondo","0019496"
---
> "0050387","nonpapillary renal cell carcinoma","mondo","0007763"
> "0050438","Frasier syndrome","mesh","D052159"
> "0050438","Frasier syndrome","umls","C0950122"
> "0050438","Frasier syndrome","mondo","0007635"
1992,1993d994
< "0080351","CLOVES syndrome","icd10cm","Q87.3"
< "0080351","CLOVES syndrome","mondo","0013038"
1997,2014c998,1023
< "0070074","autosomal dominant non-syndromic intellectual disability 44","mondo","0014892"
< "0070077","schizophrenia 1","mondo","0008414"
< "0110880","holoprosencephaly 4","mondo","0007734"
< "6354","CLL/SLL","umls","C1302547"
< "6354","CLL/SLL","mondo","0003864"
< "3770","pulmonary fibrosis","mesh","D011658"
< "3770","pulmonary fibrosis","umls","C0034069"
< "3770","pulmonary fibrosis","mondo","0002771"
< "0110735","neurodegeneration with brain iron accumulation 2a","icd10cm","G23.0"
< "0110735","neurodegeneration with brain iron accumulation 2a","mondo","0024457"
< "4527","ovarian angiosarcoma","umls","C1335152"
< "4527","ovarian angiosarcoma","mondo","0003035"
< "4830","adenosquamous carcinoma","mesh","D018196"
< "4830","adenosquamous carcinoma","umls","C0206623"
< "4830","adenosquamous carcinoma","mondo","0006074"
< "4525","mediastinum angiosarcoma","umls","C1334649"
< "4525","mediastinum angiosarcoma","mondo","0003034"
< "0110882","inflammatory bowel disease 7","mondo","0011521"
---
> "0050433","fatal familial insomnia","icd10cm","A81.83"
> "0050433","fatal familial insomnia","icd9cm","046.72"
> "0050433","fatal familial insomnia","mesh","D034062"
> "0050433","fatal familial insomnia","umls","C0206042"
> "0050433","fatal familial insomnia","mondo","0010808"
> "0050432","Asperger syndrome","icd10cm","F84.5"
> "0050432","Asperger syndrome","mesh","D020817"
> "0050432","Asperger syndrome","umls","C0236792"
> "0050432","Asperger syndrome","mondo","0005259"
> "0050431","arrhythmogenic right ventricular cardiomyopathy","mesh","D019571"
> "0050431","arrhythmogenic right ventricular cardiomyopathy","umls","C0349788"
> "0050431","arrhythmogenic right ventricular cardiomyopathy","mondo","0016587"
> "0050430","multiple endocrine neoplasia type 2A","icd10cm","E31.22"
> "0050430","multiple endocrine neoplasia type 2A","icd9cm","258.02"
> "0050430","multiple endocrine neoplasia type 2A","mesh","D018813"
> "0050430","multiple endocrine neoplasia type 2A","umls","C0025268"
> "0050430","multiple endocrine neoplasia type 2A","mondo","0008234"
> "3689","brachial plexus neuritis","icd10cm","G54.5"
> "3689","brachial plexus neuritis","mesh","D020968"
> "3689","brachial plexus neuritis","umls","C0221759"
> "3689","brachial plexus neuritis","mondo","0006682"
> "3688","plexopathy","umls","C1335437"
> "3688","plexopathy","mondo","0024432"
> "3683","lung benign neoplasm","mesh","D008175"
> "3683","lung benign neoplasm","umls","C0024121"
> "3683","lung benign neoplasm","mondo","0002732"
2019,2040c1028,1034
< "13450","coccidioidomycosis","icd10cm","B38"
< "13450","coccidioidomycosis","icd10cm","B38.9"
< "13450","coccidioidomycosis","icd9cm","114"
< "13450","coccidioidomycosis","icd9cm","114.9"
< "13450","coccidioidomycosis","mesh","D003047"
< "13450","coccidioidomycosis","umls","C0009186"
< "13450","coccidioidomycosis","mondo","0005706"
< "4520","cervical endometrial stromal sarcoma","umls","C3642326"
< "4520","cervical endometrial stromal sarcoma","mondo","0003030"
< "6196","reactive arthritis","icd10cm","M02.1"
< "6196","reactive arthritis","icd10cm","M02.10"
< "6196","reactive arthritis","icd10cm","M02.3"
< "6196","reactive arthritis","icd10cm","M02.30"
< "6196","reactive arthritis","icd9cm","099.3"
< "6196","reactive arthritis","icd9cm","711.3"
< "6196","reactive arthritis","icd9cm","711.30"
< "6196","reactive arthritis","mesh","D016918"
< "6196","reactive arthritis","umls","C0035012"
< "6196","reactive arthritis","umls","C0152085"
< "6196","reactive arthritis","mondo","0017376"
< "6190","rectum Kaposi's sarcoma","umls","C1335681"
< "6190","rectum Kaposi's sarcoma","mondo","0003796"
---
> "2518","orchitis","icd10cm","N45.2"
> "2518","orchitis","mesh","D009920"
> "2518","orchitis","umls","C0029191"
> "2518","orchitis","mondo","0006882"
> "2519","testicular disease","mesh","D013733"
> "2519","testicular disease","umls","C0039584"
> "2519","testicular disease","mondo","0002329"
2048a1043,1046
> "0111147","angioimmunoblastic T-cell lymphoma","icd10cm","C86.5"
> "0111147","angioimmunoblastic T-cell lymphoma","mesh","D007119"
> "0111147","angioimmunoblastic T-cell lymphoma","umls","C0020981"
> "0111147","angioimmunoblastic T-cell lymphoma","mondo","0004977"
2051,2054c1049,1051
< "7998","hyperthyroidism","icd10cm","E05.9"
< "7998","hyperthyroidism","mesh","D006980"
< "7998","hyperthyroidism","umls","C0020550"
< "7998","hyperthyroidism","mondo","0004425"
---
> "2516","intracranial cavernous angioma","umls","C1334237"
> "2516","intracranial cavernous angioma","mondo","0002327"
> "0111144","preterm premature rupture of the membranes","mondo","0012511"
2058,2062c1055,1059
< "0060880","renal hypomagnesemia 3","icd10cm","E83.4"
< "0060880","renal hypomagnesemia 3","mondo","0009550"
< "3457","invasive lobular carcinoma","mesh","D018275"
< "3457","invasive lobular carcinoma","umls","C0206692"
< "3457","invasive lobular carcinoma","mondo","0005051"
---
> "0111142","oligomeganephronia","icd10cm","Q60.4"
> "0111142","oligomeganephronia","mondo","0016407"
> "2512","nevoid basal cell carcinoma syndrome","mesh","D001478"
> "2512","nevoid basal cell carcinoma syndrome","umls","C0004779"
> "2512","nevoid basal cell carcinoma syndrome","mondo","0007187"
2070,2102c1067,1071
< "1094","attention deficit hyperactivity disorder","mesh","D001289"
< "1094","attention deficit hyperactivity disorder","umls","C0041671"
< "1094","attention deficit hyperactivity disorder","mondo","0005302"
< "0110631","arthrogryposis due to muscular dystrophy","icd10cm","M62.8"
< "0110631","arthrogryposis due to muscular dystrophy","mondo","0009679"
< "2730","epidermolysis bullosa","icd10cm","Q81"
< "2730","epidermolysis bullosa","icd10cm","Q81.9"
< "2730","epidermolysis bullosa","mesh","D004820"
< "2730","epidermolysis bullosa","umls","C0014527"
< "2730","epidermolysis bullosa","mondo","0006541"
< "6000","congestive heart failure","icd10cm","I50"
< "6000","congestive heart failure","icd10cm","I50.9"
< "6000","congestive heart failure","icd9cm","428"
< "6000","congestive heart failure","icd9cm","428.0"
< "6000","congestive heart failure","icd9cm","428.9"
< "6000","congestive heart failure","mesh","D006333"
< "6000","congestive heart failure","umls","C0018801"
< "6000","congestive heart failure","umls","C0018802"
< "6000","congestive heart failure","mondo","0005009"
< "5296","liver leiomyosarcoma","umls","C1333969"
< "5296","liver leiomyosarcoma","mondo","0003378"
< "5297","rectum leiomyosarcoma","umls","C1335683"
< "5297","rectum leiomyosarcoma","mondo","0003379"
< "5292","mediastinum leiomyosarcoma","umls","C1334660"
< "5292","mediastinum leiomyosarcoma","mondo","0003376"
< "2739","Gilbert syndrome","icd10cm","E80.4"
< "2739","Gilbert syndrome","mesh","D005878"
< "2739","Gilbert syndrome","umls","C0017551"
< "2739","Gilbert syndrome","mondo","0007745"
< "0110888","inflammatory bowel disease 18","mondo","0012841"
< "4769","pleuropulmonary blastoma","mesh","C537516"
< "4769","pleuropulmonary blastoma","umls","C1266144"
< "4769","pleuropulmonary blastoma","mondo","0011014"
---
> "3530","chronic wasting disease","mesh","D034081"
> "3530","chronic wasting disease","umls","C1135993"
> "3530","chronic wasting disease","mondo","0002680"
> "0050659","biotin-responsive basal ganglia disease","mesh","C537658"
> "0050659","biotin-responsive basal ganglia disease","mondo","0011841"
2104,2119c1073,1076
< "2048","autoimmune hepatitis","icd10cm","K75.4"
< "2048","autoimmune hepatitis","icd9cm","571.42"
< "2048","autoimmune hepatitis","mesh","D019693"
< "2048","autoimmune hepatitis","umls","C0241910"
< "2048","autoimmune hepatitis","umls","C1332355"
< "2048","autoimmune hepatitis","mondo","0016264"
< "9181","amebiasis","icd10cm","A06"
< "9181","amebiasis","icd10cm","A06.9"
< "9181","amebiasis","icd9cm","006"
< "9181","amebiasis","icd9cm","006.9"
< "9181","amebiasis","mesh","D000562"
< "9181","amebiasis","umls","C0002438"
< "9181","amebiasis","mondo","0005644"
< "11387","epidural abscess","mesh","D020802"
< "11387","epidural abscess","umls","C0270629"
< "11387","epidural abscess","mondo","0005752"
---
> "5058","rhabdoid meningioma","umls","C0259786"
> "5058","rhabdoid meningioma","mondo","0003262"
> "5059","childhood cerebellar neoplasm","umls","C1332959"
> "5059","childhood cerebellar neoplasm","mondo","0003263"
2126a1084,1086
> "5050","Ehrlich tumor carcinoma","mesh","D002286"
> "5050","Ehrlich tumor carcinoma","umls","C0007125"
> "5050","Ehrlich tumor carcinoma","mondo","0006739"
2133,2185c1093,1110
< "905","Zellweger syndrome","icd10cm","E71.510"
< "905","Zellweger syndrome","mesh","D015211"
< "905","Zellweger syndrome","umls","C0043459"
< "905","Zellweger syndrome","mondo","0019609"
< "0110140","Bardet-Biedl syndrome 18","icd10cm","Q87.89"
< "0110140","Bardet-Biedl syndrome 18","mondo","0014446"
< "0110141","Bardet-Biedl syndrome 19","icd10cm","Q87.89"
< "0110141","Bardet-Biedl syndrome 19","mondo","0014447"
< "0110142","Bartter disease type 1","icd10cm","E26.8"
< "0110142","Bartter disease type 1","mondo","0011127"
< "0110143","Bartter disease type 2","icd10cm","E26.8"
< "0110143","Bartter disease type 2","mondo","0009424"
< "0110144","Bartter disease type 3","icd10cm","E26.8"
< "0110144","Bartter disease type 3","mondo","0011822"
< "0110145","Bartter disease type 4a","icd10cm","E26.8"
< "0110145","Bartter disease type 4a","mondo","0011242"
< "0110146","Bartter disease type 4b","icd10cm","E26.8"
< "0110146","Bartter disease type 4b","mondo","0000909"
< "0110147","Bartter disease type 5","icd10cm","E26.8"
< "0110147","Bartter disease type 5","mondo","0010503"
< "0110148","Charcot-Marie-Tooth disease type 1A","icd10cm","G60.0"
< "0110148","Charcot-Marie-Tooth disease type 1A","mondo","0007309"
< "0110149","Charcot-Marie-Tooth disease type 1F","icd10cm","G60.0"
< "0110149","Charcot-Marie-Tooth disease type 1F","mondo","0011902"
< "11482","hemopericardium","icd9cm","423.0"
< "11482","hemopericardium","mesh","D010490"
< "11482","hemopericardium","umls","C0019064"
< "11482","hemopericardium","mondo","0005783"
< "0110782","hereditary spastic paraplegia 31","icd10cm","G11.4"
< "0110782","hereditary spastic paraplegia 31","mondo","0012453"
< "4336","tinea favosa","icd10cm","B35"
< "4336","tinea favosa","mesh","D014007"
< "4336","tinea favosa","umls","C0040254"
< "4336","tinea favosa","mondo","0005983"
< "12211","filarial elephantiasis","icd10cm","B74.0"
< "12211","filarial elephantiasis","mesh","D004605"
< "12211","filarial elephantiasis","umls","C0013884"
< "12211","filarial elephantiasis","mondo","0005761"
< "0110781","hereditary spastic paraplegia 30","icd10cm","G11.4"
< "0110781","hereditary spastic paraplegia 30","mondo","0012476"
< "0110786","hereditary spastic paraplegia 35","icd10cm","G11.4"
< "0110786","hereditary spastic paraplegia 35","mondo","0012866"
< "0110787","hereditary spastic paraplegia 36","icd10cm","G11.4"
< "0110787","hereditary spastic paraplegia 36","mondo","0013132"
< "0110784","hereditary spastic paraplegia 33","mondo","0012448"
< "0110785","hereditary spastic paraplegia 34","icd10cm","G11.4"
< "0110785","hereditary spastic paraplegia 34","mondo","0010418"
< "0060882","renal hypomagnesemia 4","icd10cm","E83.4"
< "0060882","renal hypomagnesemia 4","mondo","0012717"
< "0110788","hereditary spastic paraplegia 37","icd10cm","G11.4"
< "0110788","hereditary spastic paraplegia 37","mondo","0012766"
< "6229","childhood mature teratoma of the ovary","umls","C1332991"
< "6229","childhood mature teratoma of the ovary","mondo","0003818"
---
> "0050654","Baller-Gerold syndrome","mesh","C536788"
> "0050654","Baller-Gerold syndrome","umls","C0265308"
> "0050654","Baller-Gerold syndrome","mondo","0009039"
> "10763","hypertension","icd10cm","I10"
> "10763","hypertension","icd9cm","401-405.99"
> "10763","hypertension","icd9cm","997.91"
> "10763","hypertension","mesh","D006973"
> "10763","hypertension","umls","C0020538"
> "10763","hypertension","mondo","0005044"
> "10762","portal hypertension","icd10cm","K76.6"
> "10762","portal hypertension","icd9cm","572.3"
> "10762","portal hypertension","mesh","D006975"
> "10762","portal hypertension","umls","C0020541"
> "10762","portal hypertension","mondo","0005080"
> "0111362","hawkinsinuria","mesh","C535845"
> "0111362","hawkinsinuria","umls","C2931042"
> "0111367","Beukes hip dysplasia","mesh","C564185"
> "0111367","Beukes hip dysplasia","umls","C1840572"
2190,2193d1114
< "1156","chondrocalcinosis","icd9cm","712.1"
< "1156","chondrocalcinosis","umls","C0033802"
< "1156","chondrocalcinosis","umls","C0157852"
< "1156","chondrocalcinosis","mondo","0001314"
2210,2226c1131,1133
< "14081","toxic labyrinthitis","icd9cm","386.34"
< "14081","toxic labyrinthitis","umls","C0155507"
< "14081","toxic labyrinthitis","mondo","0001874"
< "11389","subdural empyema","mesh","D013354"
< "11389","subdural empyema","umls","C0038539"
< "11389","subdural empyema","mondo","0006984"
< "0060885","renal hypomagnesemia 2","icd10cm","E83.4"
< "0060885","renal hypomagnesemia 2","mondo","0007937"
< "10507","Dressler's syndrome","icd10cm","I24.1"
< "10507","Dressler's syndrome","icd9cm","411.0"
< "10507","Dressler's syndrome","umls","C0152107"
< "10507","Dressler's syndrome","mondo","0001049"
< "0070251","X-linked Emery-Dreifuss muscular dystrophy 6","mondo","0010401"
< "0070250","autosomal dominant Emery-Dreifuss muscular dystrophy 5","mondo","0013072"
< "0070253","congenital disorder of glycosylation type IIa","umls","C2931008"
< "0070253","congenital disorder of glycosylation type IIa","mondo","0008908"
< "0070252","autosomal dominant Emery-Dreifuss muscular dystrophy 7","mondo","0013677"
---
> "13072","acquired hyperkeratosis","icd9cm","701.1"
> "13072","acquired hyperkeratosis","umls","C0022581"
> "13072","acquired hyperkeratosis","mondo","0006522"
2229a1137,6385
> "13078","eumycotic mycetoma","icd10cm","B47"
> "13078","eumycotic mycetoma","icd10cm","B47.9"
> "13078","eumycotic mycetoma","mesh","D008271"
> "13078","eumycotic mycetoma","umls","C0024449"
> "13078","eumycotic mycetoma","mondo","0005757"
> "13891","bird fancier's lung","icd10cm","J67.2"
> "13891","bird fancier's lung","icd9cm","495.2"
> "13891","bird fancier's lung","mesh","D001716"
> "13891","bird fancier's lung","umls","C0005592"
> "13891","bird fancier's lung","mondo","0005668"
> "10184","spindle cell lipoma","umls","C0334474"
> "10184","spindle cell lipoma","mondo","0000962"
> "10187","esophageal lipoma","umls","C1333455"
> "10187","esophageal lipoma","mondo","0000963"
> "10183","endobronchial lipoma","umls","C0852937"
> "10183","endobronchial lipoma","mondo","0000961"
> "10182","diabetic peripheral angiopathy","icd9cm","250.7"
> "10182","diabetic peripheral angiopathy","umls","C0011871"
> "10182","diabetic peripheral angiopathy","mondo","0000960"
> "10188","skin lipoma","icd9cm","214.0"
> "10188","skin lipoma","umls","C0153968"
> "10188","skin lipoma","umls","C0347394"
> "10188","skin lipoma","umls","C1333174"
> "10188","skin lipoma","mondo","0000964"
> "1159","functional gastric disease","icd9cm","536.8"
> "1159","functional gastric disease","umls","C0013396"
> "1159","functional gastric disease","mondo","0001318"
> "1156","chondrocalcinosis","icd9cm","712.1"
> "1156","chondrocalcinosis","mesh","D002805"
> "1156","chondrocalcinosis","umls","C0033802"
> "1156","chondrocalcinosis","umls","C0157852"
> "1156","chondrocalcinosis","mondo","0001314"
> "14744","Partington syndrome","mesh","C562446"
> "14744","Partington syndrome","umls","C0220775"
> "14744","Partington syndrome","mondo","0010654"
> "0060258","reticulate acropigmentation of Kitamura","mesh","C562924"
> "0060258","reticulate acropigmentation of Kitamura","umls","C0406811"
> "0060258","reticulate acropigmentation of Kitamura","mondo","0014234"
> "0060259","renal-hepatic-pancreatic dysplasia","mondo","0017417"
> "0060254","Robinow syndrome","mesh","C562492"
> "0060254","Robinow syndrome","umls","C0265205"
> "0060254","Robinow syndrome","mondo","0019978"
> "0060255","rippling muscle disease 2","icd10cm","G71.0"
> "0060255","rippling muscle disease 2","mesh","C535686"
> "0060255","rippling muscle disease 2","umls","C1853698"
> "0060255","rippling muscle disease 2","mondo","0019947"
> "0060256","Dowling-Degos disease","mesh","C562924"
> "0060256","Dowling-Degos disease","umls","C0406811"
> "0060256","Dowling-Degos disease","umls","C3714534"
> "0060256","Dowling-Degos disease","mondo","0008371"
> "0060257","dyschromatosis symmetrica hereditaria","mesh","C535729"
> "0060257","dyschromatosis symmetrica hereditaria","umls","C0406775"
> "0060257","dyschromatosis symmetrica hereditaria","mondo","0007483"
> "0060250","idiopathic scoliosis","mondo","0000726"
> "0060251","sclerosteosis","mesh","C537525"
> "0060251","sclerosteosis","umls","C0265301"
> "0060251","sclerosteosis","mondo","0017838"
> "0060252","sclerocornea","mesh","C565209"
> "0060252","sclerocornea","umls","C1853235"
> "0060252","sclerocornea","mondo","0019629"
> "0060253","scapuloperoneal myopathy","mesh","C536624"
> "0060253","scapuloperoneal myopathy","mondo","0000727"
> "8036","childhood ovarian embryonal carcinoma","umls","C1332989"
> "8036","childhood ovarian embryonal carcinoma","mondo","0004441"
> "8031","pineal region meningioma","umls","C1335418"
> "8031","pineal region meningioma","mondo","0004440"
> "8030","periocular meningioma","umls","C1335383"
> "8030","periocular meningioma","mondo","0004439"
> "12859","choreatic disease","icd10cm","G25.5"
> "12859","choreatic disease","mondo","0001595"
> "12858","Huntington's disease","kegg","05016"
> "12858","Huntington's disease","icd10cm","G10"
> "12858","Huntington's disease","icd9cm","333.4"
> "12858","Huntington's disease","mesh","D006816"
> "12858","Huntington's disease","umls","C0020179"
> "12858","Huntington's disease","mondo","0007739"
> "0080105","microcephaly and chorioretinopathy 1","mondo","0009624"
> "13566","tibial collateral ligament bursitis","icd9cm","726.62"
> "13566","tibial collateral ligament bursitis","umls","C0158315"
> "13566","tibial collateral ligament bursitis","mondo","0001747"
> "12583","velocardiofacial syndrome","icd10cm","Q93.81"
> "12583","velocardiofacial syndrome","icd9cm","758.32"
> "12583","velocardiofacial syndrome","mesh","D004062"
> "12583","velocardiofacial syndrome","umls","C0220704"
> "12583","velocardiofacial syndrome","mondo","0008644"
> "12581","olecranon bursitis","icd10cm","M70.2"
> "12581","olecranon bursitis","icd9cm","726.33"
> "12581","olecranon bursitis","umls","C0263962"
> "12581","olecranon bursitis","mondo","0001557"
> "12580","Cri-Du-Chat syndrome","icd10cm","Q93.4"
> "12580","Cri-Du-Chat syndrome","icd9cm","758.31"
> "12580","Cri-Du-Chat syndrome","mesh","D003410"
> "12580","Cri-Du-Chat syndrome","umls","C0010314"
> "12580","Cri-Du-Chat syndrome","mondo","0007404"
> "8527","monocytic leukemia","icd10cm","C93"
> "8527","monocytic leukemia","icd9cm","206.8"
> "8527","monocytic leukemia","umls","C0153903"
> "8527","monocytic leukemia","mondo","0004600"
> "12857","Achilles bursitis","icd10cm","M76.6"
> "12857","Achilles bursitis","umls","C0149846"
> "12857","Achilles bursitis","mondo","0001594"
> "0060786","hypomyelinating leukodystrophy","mondo","0019046"
> "0060787","hypomyelinating leukodystrophy 2","icd10cm","E75.2"
> "0060787","hypomyelinating leukodystrophy 2","mondo","0012125"
> "0060784","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","mesh","C536189"
> "0060784","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","umls","C0406704"
> "0060784","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","mondo","0007520"
> "0060785","adult-onset autosomal dominant demyelinating leukodystrophy","umls","C3164344"
> "0060785","adult-onset autosomal dominant demyelinating leukodystrophy","mondo","0008215"
> "0060782","EEC syndrome","mesh","C536189"
> "0060782","EEC syndrome","umls","C0406704"
> "0060782","EEC syndrome","mondo","0010004"
> "0060783","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","mesh","C536189"
> "0060783","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","umls","C0406704"
> "0060783","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","mondo","0011428"
> "0060780","congenital diarrhea 6","icd10cm","P78.3"
> "0060780","congenital diarrhea 6","mondo","0013825"
> "0060781","congenital secretory sodium diarrhea 3","icd10cm","P78.3"
> "0060781","congenital secretory sodium diarrhea 3","mondo","0010036"
> "0060788","hypomyelinating leukodystrophy 10","mondo","0014632"
> "0060789","hypomyelinating leukodystrophy 4","icd10cm","E75.2"
> "0060789","hypomyelinating leukodystrophy 4","mondo","0012824"
> "3607","appendix mucinous cystadenocarcinoma","umls","C1096639"
> "3607","appendix mucinous cystadenocarcinoma","mondo","0002703"
> "0050710","3-Methylcrotonyl-CoA carboxylase deficiency","mondo","0018950"
> "13564","aspergillosis","icd10cm","B44"
> "13564","aspergillosis","icd10cm","B44.9"
> "13564","aspergillosis","icd9cm","117.3"
> "13564","aspergillosis","mesh","D001228"
> "13564","aspergillosis","umls","C0004030"
> "13564","aspergillosis","mondo","0005657"
> "0080108","myoglobinuria","mesh","D009212"
> "0080108","myoglobinuria","mondo","0000866"
> "0110122","Axenfeld-Rieger syndrome type 3","icd10cm","Q13.8"
> "0110122","Axenfeld-Rieger syndrome type 3","mondo","0011233"
> "0080109","infantile myofibromatosis","mondo","0016824"
> "0060870","isolated growth hormone deficiency","icd10cm","E23.0"
> "0060870","isolated growth hormone deficiency","icd9cm","253.3"
> "0060870","isolated growth hormone deficiency","mesh","D004393"
> "0060870","isolated growth hormone deficiency","umls","C0013338"
> "0060870","isolated growth hormone deficiency","mondo","0000050"
> "4297","scimitar syndrome","icd10cm","Q26.2"
> "4297","scimitar syndrome","icd10cm","Q26.8"
> "4297","scimitar syndrome","icd9cm","747.41"
> "4297","scimitar syndrome","mesh","D012587"
> "4297","scimitar syndrome","umls","C0036400"
> "4297","scimitar syndrome","mondo","0007130"
> "0110121","Axenfeld-Rieger syndrome type 2","icd10cm","Q13.8"
> "0110121","Axenfeld-Rieger syndrome type 2","mondo","0011097"
> "4291","fibroepithelial basal cell carcinoma","umls","C0346013"
> "4291","fibroepithelial basal cell carcinoma","mondo","0002948"
> "4290","adamantinoid basal cell epithelioma","umls","C1304295"
> "4290","adamantinoid basal cell epithelioma","mondo","0002947"
> "4293","clear cell basal cell carcinoma","umls","C1516599"
> "4293","clear cell basal cell carcinoma","mondo","0002950"
> "4292","morpheaform basal cell carcinoma","umls","C0555191"
> "4292","morpheaform basal cell carcinoma","mondo","0002949"
> "13565","neuroaspergillosis","mesh","D020953"
> "13565","neuroaspergillosis","umls","C0752342"
> "13565","neuroaspergillosis","mondo","0005873"
> "0080230","autosomal dominant mental retardation 54","mondo","0030920"
> "0080231","autosomal dominant mental retardation 52","mondo","0030918"
> "0080232","autosomal dominant mental retardation 51","mondo","0030917"
> "0080233","autosomal dominant mental retardation 50","mondo","0030916"
> "0080234","autosomal dominant mental retardation 49","mondo","0030914"
> "0080235","autosomal dominant mental retardation 48","mondo","0030913"
> "0080236","autosomal dominant mental retardation 45","mondo","0030910"
> "0080237","autosomal dominant mental retardation 46","mondo","0030911"
> "0080238","autosomal dominant mental retardation 47","mondo","0030912"
> "0080239","autosomal recessive mental retardation 61","mondo","0030915"
> "0110128","Bardet-Biedl syndrome 6","icd10cm","Q87.89"
> "0110128","Bardet-Biedl syndrome 6","mondo","0011523"
> "4749","middle cranial fossa meningioma","umls","C1334757"
> "4749","middle cranial fossa meningioma","mondo","0003121"
> "14749","methylmalonic acidemia","mondo","0002012"
> "4743","mixed testicular germ cell tumor","umls","C1336720"
> "4743","mixed testicular germ cell tumor","mondo","0003120"
> "13676","posterior scleritis","icd10cm","H15.03"
> "13676","posterior scleritis","icd9cm","379.07"
> "13676","posterior scleritis","umls","C0155357"
> "13676","posterior scleritis","mondo","0001774"
> "13677","SAPHO syndrome","mesh","D020083"
> "13677","SAPHO syndrome","umls","C0263859"
> "13677","SAPHO syndrome","mondo","0019266"
> "4744","placenta accreta","icd10cm","O43.21"
> "4744","placenta accreta","mesh","D010921"
> "4744","placenta accreta","umls","C0032044"
> "4744","placenta accreta","mondo","0005916"
> "5867","clear cell chondrosarcoma","umls","C1266167"
> "5867","clear cell chondrosarcoma","mondo","0003684"
> "5866","juxtacortical chondrosarcoma","umls","C0334549"
> "5866","juxtacortical chondrosarcoma","mondo","0003680"
> "5861","myxoid chondrosarcoma","umls","C0334551"
> "5861","myxoid chondrosarcoma","mondo","0003681"
> "5862","localized chondrosarcoma","umls","C0855011"
> "5862","localized chondrosarcoma","mondo","0003682"
> "14748","Sotos syndrome","icd10cm","Q87.3"
> "14748","Sotos syndrome","mesh","D058495"
> "14748","Sotos syndrome","umls","C0175695"
> "14748","Sotos syndrome","mondo","0019349"
> "13560","subserous uterine fibroid","icd10cm","D25.2"
> "13560","subserous uterine fibroid","icd9cm","218.2"
> "13560","subserous uterine fibroid","umls","C0153995"
> "13560","subserous uterine fibroid","mondo","0001745"
> "2181","post-surgical hypoinsulinemia","icd10cm","E89.1"
> "2181","post-surgical hypoinsulinemia","icd9cm","251.3"
> "2181","post-surgical hypoinsulinemia","umls","C0154190"
> "2181","post-surgical hypoinsulinemia","mondo","0002239"
> "0111244","palmoplantar keratoderma and congenital alopecia 1","umls","C1863093"
> "2187","amelogenesis imperfecta","icd10cm","K00.5"
> "2187","amelogenesis imperfecta","mesh","D000567"
> "2187","amelogenesis imperfecta","umls","C0002452"
> "2187","amelogenesis imperfecta","mondo","0019507"
> "4608","common bile duct neoplasm","mesh","D003138"
> "4608","common bile duct neoplasm","umls","C0009442"
> "4608","common bile duct neoplasm","mondo","0006709"
> "4606","bile duct cancer","icd10cm","C24.0"
> "4606","bile duct cancer","icd9cm","156.1"
> "4606","bile duct cancer","mesh","D001650"
> "4606","bile duct cancer","umls","C0005396"
> "4606","bile duct cancer","umls","C0153453"
> "4606","bile duct cancer","mondo","0003059"
> "4607","biliary tract cancer","icd10cm","C24.9"
> "4607","biliary tract cancer","icd9cm","156.9"
> "4607","biliary tract cancer","mesh","D001661"
> "4607","biliary tract cancer","umls","C0005426"
> "4607","biliary tract cancer","umls","C0750952"
> "4607","biliary tract cancer","mondo","0003060"
> "13515","tuberous sclerosis","icd10cm","Q85.1"
> "13515","tuberous sclerosis","icd9cm","759.5"
> "13515","tuberous sclerosis","mesh","D014402"
> "13515","tuberous sclerosis","umls","C0041341"
> "13515","tuberous sclerosis","mondo","0001734"
> "13514","venous tributary occlusion of retina","icd9cm","362.36"
> "13514","venous tributary occlusion of retina","umls","C0154842"
> "13514","venous tributary occlusion of retina","mondo","0001733"
> "4603","epidermolytic hyperkeratosis","icd10cm","Q80.3"
> "4603","epidermolytic hyperkeratosis","mesh","D017488"
> "4603","epidermolytic hyperkeratosis","umls","C0079153"
> "4603","epidermolytic hyperkeratosis","mondo","0007239"
> "12685","mixed receptive-expressive language disorder","icd10cm","F80.2"
> "12685","mixed receptive-expressive language disorder","icd9cm","315.32"
> "12685","mixed receptive-expressive language disorder","umls","C0236827"
> "12685","mixed receptive-expressive language disorder","mondo","0001568"
> "6906","glomangiomatosis","umls","C1333824"
> "6906","glomangiomatosis","mondo","0004035"
> "12239","anal margin squamous cell carcinoma","icd10cm","C44.520"
> "12239","anal margin squamous cell carcinoma","umls","C1412037"
> "12239","anal margin squamous cell carcinoma","mondo","0001470"
> "2231","factor XII deficiency","mesh","D005175"
> "2231","factor XII deficiency","umls","C0015526"
> "2231","factor XII deficiency","mondo","0009315"
> "13918","somatization disorder","icd10cm","F45.0"
> "13918","somatization disorder","icd9cm","300.81"
> "13918","somatization disorder","mesh","D013001"
> "13918","somatization disorder","umls","C0520482"
> "13918","somatization disorder","mondo","0001830"
> "6903","eye lymphoma","umls","C1333519"
> "6903","eye lymphoma","mondo","0004034"
> "150","disease of mental health","icd10cm","F99"
> "150","disease of mental health","icd10cm","F99-F99"
> "150","disease of mental health","mesh","D001523"
> "150","disease of mental health","umls","C0004936"
> "150","disease of mental health","mondo","0002025"
> "2533","splenic infarction","icd10cm","D73.5"
> "2533","splenic infarction","mesh","D013159"
> "2533","splenic infarction","umls","C0037998"
> "2533","splenic infarction","mondo","0006978"
> "154","mixed cell type cancer","mesh","D018198"
> "154","mixed cell type cancer","umls","C0206625"
> "154","mixed cell type cancer","umls","C1368354"
> "154","mixed cell type cancer","mondo","0005853"
> "2235","prothrombin deficiency","mesh","D007020"
> "2235","prothrombin deficiency","umls","C0020640"
> "2235","prothrombin deficiency","mondo","0013361"
> "0111007","X-linked cone-rod dystrophy 3","mondo","0010335"
> "13913","lumbosacral plexus lesion","icd9cm","353.1"
> "13913","lumbosacral plexus lesion","umls","C0154735"
> "13913","lumbosacral plexus lesion","mondo","0001829"
> "2237","hepatitis","icd10cm","K73.9"
> "2237","hepatitis","icd9cm","570"
> "2237","hepatitis","icd9cm","571.4"
> "2237","hepatitis","icd9cm","571.40"
> "2237","hepatitis","icd9cm","571.41"
> "2237","hepatitis","mesh","D006505"
> "2237","hepatitis","mesh","D006521"
> "2237","hepatitis","umls","C0001308"
> "2237","hepatitis","umls","C0019189"
> "2237","hepatitis","umls","C0149519"
> "2237","hepatitis","mondo","0002251"
> "6458","cerebellar liponeurocytoma","umls","C1370507"
> "6458","cerebellar liponeurocytoma","mondo","0006131"
> "0111005","cone-rod dystrophy 2","mondo","0007362"
> "2530","splenic abscess","icd10cm","D73.3"
> "2530","splenic abscess","umls","C0272412"
> "2530","splenic abscess","mondo","0002333"
> "8689","anorexia nervosa","icd10cm","F50.0"
> "8689","anorexia nervosa","icd10cm","F50.00"
> "8689","anorexia nervosa","icd9cm","307.1"
> "8689","anorexia nervosa","mesh","D000856"
> "8689","anorexia nervosa","umls","C0003125"
> "8689","anorexia nervosa","mondo","0005351"
> "0111247","hypertension and brachydactyly syndrome","umls","C1862170"
> "3762","cytochrome-c oxidase deficiency disease","mesh","D030401"
> "3762","cytochrome-c oxidase deficiency disease","umls","C0268237"
> "3762","cytochrome-c oxidase deficiency disease","mondo","0009068"
> "2725","capillary hemangioma","icd10cm","Q82.5"
> "2725","capillary hemangioma","mesh","D018324"
> "2725","capillary hemangioma","umls","C0206733"
> "2725","capillary hemangioma","mondo","0002407"
> "2723","dermatitis","icd10cm","L30.9"
> "2723","dermatitis","mesh","D003872"
> "2723","dermatitis","umls","C0011603"
> "2723","dermatitis","mondo","0002406"
> "2722","acrodermatitis","mesh","D000169"
> "2722","acrodermatitis","umls","C0001197"
> "2722","acrodermatitis","mondo","0006523"
> "2729","dyskeratosis congenita","mesh","D019871"
> "2729","dyskeratosis congenita","umls","C0265965"
> "2729","dyskeratosis congenita","mondo","0015780"
> "7236","pancreatic invasive mucinous cystadenocarcinoma","umls","C1518870"
> "7236","pancreatic invasive mucinous cystadenocarcinoma","mondo","0004158"
> "7237","pancreatic non-invasive mucinous cystadenocarcinoma","umls","C1518874"
> "7237","pancreatic non-invasive mucinous cystadenocarcinoma","mondo","0004159"
> "7234","pancreatic colloid cystadenocarcinoma","umls","C1335308"
> "7234","pancreatic colloid cystadenocarcinoma","mondo","0004156"
> "7235","pancreatic mucinous cystadenoma","umls","C1518872"
> "7235","pancreatic mucinous cystadenoma","mondo","0018523"
> "7232","central nervous system embryonal carcinoma","umls","C1333377"
> "7232","central nervous system embryonal carcinoma","mondo","0018843"
> "7233","adult central nervous system embryonal carcinoma","umls","C1370503"
> "7233","adult central nervous system embryonal carcinoma","mondo","0004155"
> "7230","postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma","umls","C1333037"
> "7230","postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma","mondo","0004152"
> "7231","pediatric CNS embryonal cell carcinoma","umls","C1377605"
> "7231","pediatric CNS embryonal cell carcinoma","mondo","0004153"
> "10376","amblyopia","icd10cm","H53.00"
> "10376","amblyopia","icd9cm","368.00"
> "10376","amblyopia","mesh","D000550"
> "10376","amblyopia","umls","C0002418"
> "10376","amblyopia","mondo","0001020"
> "10377","ametropic amblyopia","icd10cm","H53.02"
> "10377","ametropic amblyopia","icd9cm","368.03"
> "10377","ametropic amblyopia","umls","C0152190"
> "10377","ametropic amblyopia","mondo","0001021"
> "10375","suppression amblyopia","icd10cm","H53.03"
> "10375","suppression amblyopia","icd9cm","368.01"
> "10375","suppression amblyopia","mesh","D000550"
> "10375","suppression amblyopia","umls","C0750903"
> "10375","suppression amblyopia","mondo","0001019"
> "7949","stroma-dominant and stroma-poor composite ganglioneuroblastoma","umls","C1516761"
> "7949","stroma-dominant and stroma-poor composite ganglioneuroblastoma","mondo","0004407"
> "10371","yaws","icd10cm","A66"
> "10371","yaws","icd10cm","A66.9"
> "10371","yaws","icd9cm","102"
> "10371","yaws","icd9cm","102.9"
> "10371","yaws","mesh","D015001"
> "10371","yaws","umls","C0043388"
> "10371","yaws","mondo","0006019"
> "0110715","congenital stationary night blindness autosomal dominant 3","mondo","0012497"
> "0110179","Charcot-Marie-Tooth disease type 2B2","icd10cm","G60.0"
> "0110179","Charcot-Marie-Tooth disease type 2B2","mondo","0011570"
> "0110178","Charcot-Marie-Tooth disease axonal type 2V","mondo","0014665"
> "0110175","Charcot-Marie-Tooth disease axonal type 2O","icd10cm","G60.0"
> "0110175","Charcot-Marie-Tooth disease axonal type 2O","mondo","0013644"
> "0110174","Charcot-Marie-Tooth disease axonal type 2L","icd10cm","G60.0"
> "0110174","Charcot-Marie-Tooth disease axonal type 2L","mondo","0012096"
> "0110177","Charcot-Marie-Tooth disease axonal type 2N","icd10cm","G60.0"
> "0110177","Charcot-Marie-Tooth disease axonal type 2N","mondo","0013212"
> "0110176","Charcot-Marie-Tooth disease axonal type 2X","mondo","0014726"
> "0110171","Charcot-Marie-Tooth disease axonal type 2S","mondo","0014511"
> "9296","cleft lip","icd10cm","Q36"
> "9296","cleft lip","icd10cm","Q36.9"
> "9296","cleft lip","icd9cm","749.1"
> "9296","cleft lip","icd9cm","749.10"
> "9296","cleft lip","icd9cm","749.11"
> "9296","cleft lip","mesh","D002971"
> "9296","cleft lip","umls","C0008924"
> "9296","cleft lip","umls","C0158651"
> "9296","cleft lip","mondo","0004747"
> "0110173","Charcot-Marie-Tooth disease axonal type 2U","icd10cm","G60.0"
> "0110173","Charcot-Marie-Tooth disease axonal type 2U","mondo","0014566"
> "6239","non-invasive bladder papillary urothelial neoplasm","umls","C1266010"
> "6239","non-invasive bladder papillary urothelial neoplasm","umls","C1518358"
> "6239","non-invasive bladder papillary urothelial neoplasm","mondo","0003822"
> "10567","late yaws","icd10cm","A66.1"
> "10567","late yaws","icd10cm","A66.4"
> "10567","late yaws","icd9cm","102.1"
> "10567","late yaws","icd9cm","102.4"
> "10567","late yaws","umls","C0153234"
> "10567","late yaws","umls","C0276007"
> "10567","late yaws","umls","C1517744"
> "10567","late yaws","mondo","0001066"
> "12206","dengue hemorrhagic fever","icd10cm","A91"
> "12206","dengue hemorrhagic fever","mesh","D019595"
> "12206","dengue hemorrhagic fever","umls","C0019100"
> "12206","dengue hemorrhagic fever","mondo","0005358"
> "6231","mature teratoma of the ovary","umls","C1334637"
> "6231","mature teratoma of the ovary","mondo","0003820"
> "6230","childhood teratoma of the ovary","umls","C1332992"
> "6230","childhood teratoma of the ovary","mondo","0003819"
> "6232","ovarian biphasic or triphasic teratoma","umls","C1518691"
> "6232","ovarian biphasic or triphasic teratoma","mondo","0003821"
> "10518","beach ear","icd9cm","380.12"
> "10518","beach ear","umls","C0155393"
> "10518","beach ear","mondo","0001051"
> "10519","chronic fungal otitis externa","icd9cm","380.15"
> "10519","chronic fungal otitis externa","umls","C0155396"
> "10519","chronic fungal otitis externa","mondo","0001052"
> "9779","bowel dysfunction","icd10cm","K59.9"
> "9779","bowel dysfunction","icd9cm","564.9"
> "9779","bowel dysfunction","umls","C0016807"
> "9779","bowel dysfunction","mondo","0004880"
> "9778","irritable bowel syndrome","kegg","05321"
> "9778","irritable bowel syndrome","icd10cm","K58"
> "9778","irritable bowel syndrome","icd10cm","K58.9"
> "9778","irritable bowel syndrome","icd9cm","564.1"
> "9778","irritable bowel syndrome","mesh","D043183"
> "9778","irritable bowel syndrome","umls","C0022104"
> "9778","irritable bowel syndrome","mondo","0005052"
> "9775","diastolic heart failure","icd10cm","I50.30"
> "9775","diastolic heart failure","icd9cm","428.3"
> "9775","diastolic heart failure","icd9cm","428.30"
> "9775","diastolic heart failure","mesh","D054144"
> "9775","diastolic heart failure","umls","C1135196"
> "9775","diastolic heart failure","mondo","0006727"
> "9776","Senile atrophy of choroid","icd9cm","363.41"
> "9776","Senile atrophy of choroid","umls","C0154891"
> "9776","Senile atrophy of choroid","mondo","0004879"
> "9771","transient neonatal thrombocytopenia","icd10cm","P61.0"
> "9771","transient neonatal thrombocytopenia","icd9cm","776.1"
> "9771","transient neonatal thrombocytopenia","umls","C0158991"
> "9771","transient neonatal thrombocytopenia","mondo","0004877"
> "9773","female breast upper-outer quadrant cancer","icd10cm","C50.41"
> "9773","female breast upper-outer quadrant cancer","icd9cm","174.4"
> "9773","female breast upper-outer quadrant cancer","umls","C0153552"
> "9773","female breast upper-outer quadrant cancer","mondo","0004878"
> "8866","actinic keratosis","icd10cm","L57.0"
> "8866","actinic keratosis","icd9cm","702.0"
> "8866","actinic keratosis","mesh","D055623"
> "8866","actinic keratosis","umls","C0022602"
> "8866","actinic keratosis","mondo","0005173"
> "8867","molluscum contagiosum","icd10cm","B08.1"
> "8867","molluscum contagiosum","icd9cm","078.0"
> "8867","molluscum contagiosum","mesh","D008976"
> "8867","molluscum contagiosum","umls","C0026393"
> "8867","molluscum contagiosum","mondo","0005855"
> "8864","acute monocytic leukemia","icd9cm","206.0"
> "8864","acute monocytic leukemia","mesh","D007948"
> "8864","acute monocytic leukemia","umls","C0023465"
> "8864","acute monocytic leukemia","mondo","0007896"
> "0111243","acromicric dysplasia","mesh","C535662"
> "0111243","acromicric dysplasia","umls","C0265287"
> "8861","pulmonary subvalvular stenosis","icd10cm","Q24.3"
> "8861","pulmonary subvalvular stenosis","icd9cm","746.83"
> "8861","pulmonary subvalvular stenosis","mesh","D011662"
> "8861","pulmonary subvalvular stenosis","umls","C0034084"
> "8861","pulmonary subvalvular stenosis","mondo","0006935"
> "0080365","endometrial hyperplasia","mesh","D004714"
> "8869","neuromyelitis optica","icd10cm","G36.0"
> "8869","neuromyelitis optica","icd9cm","341.0"
> "8869","neuromyelitis optica","mesh","D009471"
> "8869","neuromyelitis optica","umls","C0027873"
> "8869","neuromyelitis optica","mondo","0019100"
> "819","mediastinitis","icd10cm","J98.51"
> "819","mediastinitis","icd9cm","519.2"
> "819","mediastinitis","mesh","D008480"
> "819","mediastinitis","umls","C0025064"
> "819","mediastinitis","mondo","0004492"
> "811","lipodystrophy","icd10cm","E88.1"
> "811","lipodystrophy","icd9cm","272.6"
> "811","lipodystrophy","mesh","D008060"
> "811","lipodystrophy","umls","C0023787"
> "811","lipodystrophy","mondo","0006573"
> "813","septic arthritis","icd10cm","M00"
> "813","septic arthritis","icd10cm","M00.9"
> "813","septic arthritis","icd9cm","711.0"
> "813","septic arthritis","icd9cm","711.9"
> "813","septic arthritis","icd9cm","711.90"
> "813","septic arthritis","icd9cm","711.91"
> "813","septic arthritis","icd9cm","711.92"
> "813","septic arthritis","icd9cm","711.93"
> "813","septic arthritis","icd9cm","711.94"
> "813","septic arthritis","icd9cm","711.95"
> "813","septic arthritis","icd9cm","711.96"
> "813","septic arthritis","icd9cm","711.97"
> "813","septic arthritis","mesh","D001170"
> "813","septic arthritis","umls","C0003869"
> "813","septic arthritis","umls","C0157843"
> "813","septic arthritis","umls","C0157844"
> "813","septic arthritis","umls","C0157845"
> "813","septic arthritis","umls","C0157846"
> "813","septic arthritis","umls","C0157847"
> "813","septic arthritis","umls","C0157848"
> "813","septic arthritis","umls","C0157849"
> "813","septic arthritis","mondo","0004471"
> "817","interstitial myocarditis","umls","C0027060"
> "817","interstitial myocarditis","mondo","0004485"
> "7733","signet ring cell intrahepatic cholangiocarcinoma","umls","C1519321"
> "7733","signet ring cell intrahepatic cholangiocarcinoma","mondo","0004346"
> "0060178","familial hemiplegic migraine","icd10cm","G43.8"
> "0060178","familial hemiplegic migraine","icd9cm","346.8"
> "0060178","familial hemiplegic migraine","umls","C0477373"
> "0060178","familial hemiplegic migraine","mondo","0000700"
> "5267","anus leiomyosarcoma","umls","C1332267"
> "5267","anus leiomyosarcoma","mondo","0003358"
> "1701","steroid inherited metabolic disorder","mesh","D043202"
> "1701","steroid inherited metabolic disorder","umls","C1257809"
> "1701","steroid inherited metabolic disorder","mondo","0005523"
> "5265","lung leiomyosarcoma","umls","C1334448"
> "5265","lung leiomyosarcoma","mondo","0003357"
> "5264","epithelioid leiomyosarcoma","mesh","D007890"
> "5264","epithelioid leiomyosarcoma","umls","C0205815"
> "5264","epithelioid leiomyosarcoma","mondo","0003356"
> "5263","ovary leiomyosarcoma","umls","C1335163"
> "5263","ovary leiomyosarcoma","mondo","0003355"
> "5262","heart sarcoma","umls","C0238152"
> "5262","heart sarcoma","mondo","0003354"
> "5261","heart leiomyosarcoma","umls","C1332848"
> "5261","heart leiomyosarcoma","mondo","0003353"
> "5260","colon sarcoma","umls","C1333098"
> "5260","colon sarcoma","mondo","0003352"
> "14181","calcific tendinitis","icd10cm","M75.3"
> "14181","calcific tendinitis","icd9cm","726.11"
> "14181","calcific tendinitis","umls","C0158303"
> "14181","calcific tendinitis","mondo","0001903"
> "14183","alcoholic neuropathy","icd10cm","G62.1"
> "14183","alcoholic neuropathy","icd9cm","357.5"
> "14183","alcoholic neuropathy","mesh","D020269"
> "14183","alcoholic neuropathy","umls","C0085677"
> "14183","alcoholic neuropathy","mondo","0006645"
> "14184","polyneuropathy due to drug","icd10cm","G62.0"
> "14184","polyneuropathy due to drug","icd9cm","357.6"
> "14184","polyneuropathy due to drug","umls","C0154762"
> "14184","polyneuropathy due to drug","mondo","0001904"
> "5268","myxoid leiomyosarcoma","mesh","D007890"
> "5268","myxoid leiomyosarcoma","umls","C0205816"
> "5268","myxoid leiomyosarcoma","mondo","0003359"
> "13402","skin sarcoidosis","icd10cm","D86.3"
> "13402","skin sarcoidosis","umls","C0036203"
> "13402","skin sarcoidosis","mondo","0006611"
> "2093","vulvar melanoma","umls","C0241989"
> "2093","vulvar melanoma","mondo","0002205"
> "2092","transient arthritis","icd10cm","M12.8"
> "2092","transient arthritis","icd9cm","716.4"
> "2092","transient arthritis","icd9cm","716.40"
> "2092","transient arthritis","umls","C0152083"
> "2092","transient arthritis","mondo","0002204"
> "14325","mixed malaria","icd9cm","084.5"
> "14325","mixed malaria","umls","C0153121"
> "14325","mixed malaria","mondo","0001944"
> "0080198","infantile histiocytoid cardiomyopathy","mondo","0010771"
> "11134","prolapse of lacrimal gland","icd10cm","H04.16"
> "11134","prolapse of lacrimal gland","icd9cm","375.16"
> "11134","prolapse of lacrimal gland","umls","C0155231"
> "11134","prolapse of lacrimal gland","mondo","0001203"
> "11133","prostatic cyst","icd10cm","N42.83"
> "11133","prostatic cyst","icd9cm","600.3"
> "11133","prostatic cyst","umls","C1443972"
> "11133","prostatic cyst","mondo","0001202"
> "0110713","Oguchi disease-2","mondo","0013259"
> "14323","Marfan syndrome","icd10cm","Q87.4"
> "14323","Marfan syndrome","icd10cm","Q87.40"
> "14323","Marfan syndrome","icd9cm","759.82"
> "14323","Marfan syndrome","mesh","D008382"
> "14323","Marfan syndrome","umls","C0024796"
> "14323","Marfan syndrome","mondo","0007947"
> "11130","secondary hypertension","icd10cm","I15"
> "11130","secondary hypertension","icd10cm","I15.9"
> "11130","secondary hypertension","icd9cm","405"
> "11130","secondary hypertension","icd9cm","405.9"
> "11130","secondary hypertension","umls","C0155616"
> "11130","secondary hypertension","mondo","0001200"
> "14459","hemangioma of orbit","umls","C1335128"
> "14459","hemangioma of orbit","mondo","0001974"
> "3029","colon mucinous adenocarcinoma","umls","C0279639"
> "3029","colon mucinous adenocarcinoma","mondo","0005007"
> "3025","acinar cell carcinoma","mesh","D018267"
> "3025","acinar cell carcinoma","umls","C0206685"
> "3025","acinar cell carcinoma","mondo","0004965"
> "3024","prostatic acinar adenocarcinoma","umls","C1332139"
> "3024","prostatic acinar adenocarcinoma","mondo","0002493"
> "3021","acute kidney failure","mesh","D058186"
> "3021","acute kidney failure","mondo","0002492"
> "8738","leukoplakia of penis","icd10cm","N48.0"
> "8738","leukoplakia of penis","icd9cm","607.0"
> "8738","leukoplakia of penis","mesh","D052798"
> "8738","leukoplakia of penis","umls","C0022782"
> "8738","leukoplakia of penis","mondo","0006830"
> "8736","smallpox","icd10cm","B03"
> "8736","smallpox","icd9cm","050"
> "8736","smallpox","icd9cm","050.9"
> "8736","smallpox","mesh","D012899"
> "8736","smallpox","umls","C0037354"
> "8736","smallpox","mondo","0004651"
> "0111248","cerebrocostomandibular syndrome","umls","C0265342"
> "8731","carotid body cancer","icd10cm","C75.4"
> "8731","carotid body cancer","icd9cm","194.5"
> "8731","carotid body cancer","umls","C0153656"
> "8731","carotid body cancer","mondo","0004650"
> "0060445","congenital stromal corneal dystrophy","icd10cm","H18.5"
> "0060445","congenital stromal corneal dystrophy","mesh","C566452"
> "0060445","congenital stromal corneal dystrophy","mondo","0012401"
> "0060444","granular corneal dystrophy 2","mesh","C535474"
> "0060444","granular corneal dystrophy 2","umls","C1275685"
> "0060444","granular corneal dystrophy 2","mondo","0011855"
> "0060447","epithelial basement membrane dystrophy","icd10cm","H18.5"
> "0060447","epithelial basement membrane dystrophy","mesh","C535477"
> "0060447","epithelial basement membrane dystrophy","mondo","0007375"
> "0060446","X-linked endothelial corneal dystrophy","icd10cm","H18.5"
> "0060446","X-linked endothelial corneal dystrophy","mesh","C567587"
> "0060446","X-linked endothelial corneal dystrophy","mondo","0010426"
> "4196","femoral neuropathy","icd10cm","G57.2"
> "4196","femoral neuropathy","icd10cm","G57.20"
> "4196","femoral neuropathy","mesh","D020428"
> "4196","femoral neuropathy","umls","C0751931"
> "4196","femoral neuropathy","mondo","0006759"
> "0060448","Fleck corneal dystrophy","mesh","C563256"
> "0060448","Fleck corneal dystrophy","umls","C1562113"
> "0060448","Fleck corneal dystrophy","mondo","0007376"
> "4194","glucose metabolism disease","mesh","D044882"
> "4194","glucose metabolism disease","umls","C1257958"
> "4194","glucose metabolism disease","mondo","0002908"
> "4195","hyperglycemia","icd10cm","R73.9"
> "4195","hyperglycemia","mesh","D006943"
> "4195","hyperglycemia","umls","C0020456"
> "4195","hyperglycemia","mondo","0002909"
> "4193","intracranial thrombosis","icd9cm","434.0"
> "4193","intracranial thrombosis","mesh","D020767"
> "4193","intracranial thrombosis","umls","C0079102"
> "4193","intracranial thrombosis","umls","C0752143"
> "4193","intracranial thrombosis","mondo","0002907"
> "13861","scleroperikeratitis","icd10cm","H15.04"
> "13861","scleroperikeratitis","icd9cm","379.05"
> "13861","scleroperikeratitis","umls","C0155355"
> "13861","scleroperikeratitis","mondo","0001816"
> "5670","comedo carcinoma","umls","C0334370"
> "5670","comedo carcinoma","mondo","0003575"
> "5672","large intestine cancer","icd10cm","C18.9"
> "5672","large intestine cancer","mesh","D015179"
> "5672","large intestine cancer","umls","C0009402"
> "5672","large intestine cancer","umls","C0346629"
> "5672","large intestine cancer","umls","C1319315"
> "5672","large intestine cancer","mondo","0005575"
> "11664","nephrosclerosis","icd10cm","I12"
> "11664","nephrosclerosis","icd10cm","N26.9"
> "11664","nephrosclerosis","icd9cm","587"
> "11664","nephrosclerosis","mesh","D009400"
> "11664","nephrosclerosis","umls","C0027719"
> "11664","nephrosclerosis","mondo","0006044"
> "5675","cribriform carcinoma","mesh","D000230"
> "5675","cribriform carcinoma","umls","C0205643"
> "5675","cribriform carcinoma","mondo","0045059"
> "5677","extragonadal nonseminomatous germ cell tumor","umls","C1334582"
> "5677","extragonadal nonseminomatous germ cell tumor","mondo","0003578"
> "5678","nerve fibre bundle defect","icd9cm","362.85"
> "5678","nerve fibre bundle defect","umls","C0474334"
> "5678","nerve fibre bundle defect","mondo","0003579"
> "5679","retinal disease","icd10cm","H35.9"
> "5679","retinal disease","icd9cm","362.9"
> "5679","retinal disease","mesh","D012164"
> "5679","retinal disease","umls","C0035309"
> "5679","retinal disease","mondo","0005283"
> "11661","blue color blindness","icd10cm","H53.55"
> "11661","blue color blindness","icd9cm","368.53"
> "11661","blue color blindness","mesh","D003117"
> "11661","blue color blindness","umls","C0155017"
> "11661","blue color blindness","mondo","0008610"
> "8193","papillary pattern testicular yolk sac tumor","umls","C1515310"
> "8193","papillary pattern testicular yolk sac tumor","mondo","0004493"
> "12445","conjugate gaze palsy","icd9cm","378.81"
> "12445","conjugate gaze palsy","umls","C0702143"
> "12445","conjugate gaze palsy","mondo","0001527"
> "6432","pulmonary hypertension","icd10cm","I27.20"
> "6432","pulmonary hypertension","mesh","D006976"
> "6432","pulmonary hypertension","umls","C0020542"
> "6432","pulmonary hypertension","mondo","0005149"
> "10691","fat necrosis of breast","icd10cm","N64.1"
> "10691","fat necrosis of breast","icd9cm","611.3"
> "10691","fat necrosis of breast","umls","C0156321"
> "10691","fat necrosis of breast","mondo","0001101"
> "8195","hepatoid pattern testicular yolk sac tumor","umls","C1515306"
> "8195","hepatoid pattern testicular yolk sac tumor","mondo","0004494"
> "12449","aplastic anemia","icd10cm","D61.9"
> "12449","aplastic anemia","icd9cm","284.9"
> "12449","aplastic anemia","mesh","D000741"
> "12449","aplastic anemia","umls","C0002874"
> "12449","aplastic anemia","mondo","0015909"
> "10690","mastitis","mesh","D008413"
> "10690","mastitis","umls","C0024894"
> "10690","mastitis","mondo","0006849"
> "0110999","Joubert syndrome 4","mesh","C536296"
> "0110999","Joubert syndrome 4","mondo","0012308"
> "0110998","Joubert syndrome 3","mesh","C536295"
> "0110998","Joubert syndrome 3","mondo","0012078"
> "0110997","Joubert syndrome 28","mondo","0014928"
> "0110996","Joubert syndrome 27","mondo","0014927"
> "0110995","Joubert syndrome 26","mondo","0014771"
> "0110994","Joubert syndrome 25","mondo","0014770"
> "0110993","Joubert syndrome 24","mondo","0014724"
> "0110992","Joubert syndrome 23","mondo","0014664"
> "0110991","Joubert syndrome 22","mondo","0014297"
> "0110990","Joubert syndrome 21","mondo","0014288"
> "6758","chest wall lymphoma","umls","C0346948"
> "6758","chest wall lymphoma","umls","C1332933"
> "6758","chest wall lymphoma","mondo","0003985"
> "6759","bone lymphoma","umls","C1332582"
> "6759","bone lymphoma","mondo","0017814"
> "6752","internal auditory canal lipoma","umls","C1334226"
> "6752","internal auditory canal lipoma","mondo","0003984"
> "6755","amyloid tumor","umls","C0333572"
> "6755","amyloid tumor","mondo","0024892"
> "9942","lymph node disease","umls","C0272394"
> "9942","lymph node disease","mondo","0004928"
> "9946","steroid-induced glaucoma","icd9cm","365.3"
> "9946","steroid-induced glaucoma","umls","C0339578"
> "9946","steroid-induced glaucoma","mondo","0004930"
> "9945","constant exophthalmos","icd10cm","H05.24"
> "9945","constant exophthalmos","icd9cm","376.31"
> "9945","constant exophthalmos","umls","C0155267"
> "9945","constant exophthalmos","mondo","0004929"
> "9948","residual stage corticosteroid-induced glaucoma","icd9cm","365.32"
> "9948","residual stage corticosteroid-induced glaucoma","umls","C0339580"
> "9948","residual stage corticosteroid-induced glaucoma","mondo","0004931"
> "0060863","patterned macular dystrophy","icd10cm","H35.5"
> "0060863","patterned macular dystrophy","mondo","0020381"
> "0060862","mal de Meleda","icd10cm","Q82.8"
> "0060862","mal de Meleda","mondo","0009552"
> "0060861","microphthalmia with limb anomalies","icd10cm","Q87.2"
> "0060861","microphthalmia with limb anomalies","mondo","0008800"
> "0060867","macrocephaly-autism syndrome","mondo","0011537"
> "0060866","patterned macular dystrophy 1","mondo","0008210"
> "0060865","patterned macular dystrophy 3","mondo","0014920"
> "0060864","patterned macular dystrophy 2","mondo","0012162"
> "0060869","late-onset retinal degeneration","mondo","0011579"
> "0060868","leukoencephalopathy with vanishing white matter","icd10cm","E75.2"
> "0060868","leukoencephalopathy with vanishing white matter","mondo","0011380"
> "12053","cryptococcosis","icd10cm","B45"
> "12053","cryptococcosis","icd10cm","B45.9"
> "12053","cryptococcosis","icd9cm","117.5"
> "12053","cryptococcosis","mesh","D003453"
> "12053","cryptococcosis","umls","C0010414"
> "12053","cryptococcosis","mondo","0005724"
> "12055","sarcoid meningitis","icd10cm","D86.81"
> "12055","sarcoid meningitis","icd9cm","321.4"
> "12055","sarcoid meningitis","umls","C0154648"
> "12055","sarcoid meningitis","mondo","0001424"
> "234","colon adenocarcinoma","umls","C0338106"
> "234","colon adenocarcinoma","mondo","0002271"
> "235","colonic benign neoplasm","mesh","D003110"
> "235","colonic benign neoplasm","umls","C0009375"
> "235","colonic benign neoplasm","mondo","0002278"
> "230","lateral sclerosis","icd10cm","G12.23"
> "230","lateral sclerosis","icd9cm","335.24"
> "230","lateral sclerosis","mesh","D016472"
> "230","lateral sclerosis","umls","C0154682"
> "230","lateral sclerosis","mondo","0018155"
> "231","motor neuron disease","icd10cm","G12.2"
> "231","motor neuron disease","icd10cm","G12.20"
> "231","motor neuron disease","icd9cm","335.2"
> "231","motor neuron disease","mesh","D016472"
> "231","motor neuron disease","umls","C0085084"
> "231","motor neuron disease","mondo","0020128"
> "14687","diastrophic dysplasia","icd10cm","Q77.5"
> "14687","diastrophic dysplasia","mesh","C536170"
> "14687","diastrophic dysplasia","umls","C0220726"
> "14687","diastrophic dysplasia","mondo","0009107"
> "0050419","complement factor I deficiency","mesh","C572568"
> "0050419","complement factor I deficiency","mondo","0012594"
> "10697","chronic endophthalmitis","icd9cm","360.03"
> "10697","chronic endophthalmitis","umls","C0154774"
> "10697","chronic endophthalmitis","mondo","0017203"
> "0111169","subcortical band heterotopia","mesh","D054221"
> "0111169","subcortical band heterotopia","umls","C1848201"
> "0111169","subcortical band heterotopia","mondo","0020491"
> "0111168","sepiapterin reductase deficiency","mesh","C562657"
> "0111168","sepiapterin reductase deficiency","umls","C0268468"
> "0111168","sepiapterin reductase deficiency","mondo","0012994"
> "2538","Landau-Kleffner syndrome","icd10cm","G40.8"
> "2538","Landau-Kleffner syndrome","mesh","D018887"
> "2538","Landau-Kleffner syndrome","umls","C0282512"
> "2538","Landau-Kleffner syndrome","mondo","0009509"
> "0111161","Crouzon syndrome-acanthosis nigricans syndrome","mondo","0012833"
> "0111160","camptodactyly-tall stature-scoliosis-hearing loss syndrome","mesh","C537975"
> "0111160","camptodactyly-tall stature-scoliosis-hearing loss syndrome","umls","C1864852"
> "0111160","camptodactyly-tall stature-scoliosis-hearing loss syndrome","mondo","0012504"
> "0111163","molybdenum cofactor deficiency type B","mesh","C565373"
> "0111163","molybdenum cofactor deficiency type B","umls","C1854989"
> "0111163","molybdenum cofactor deficiency type B","mondo","0009644"
> "2531","hematologic cancer","mesh","D019337"
> "2531","hematologic cancer","umls","C0376544"
> "2531","hematologic cancer","mondo","0002334"
> "0111165","molybdenum cofactor deficiency","icd10cm","E72.1"
> "0111165","molybdenum cofactor deficiency","mondo","0020480"
> "2537","inflammatory and toxic neuropathy","icd9cm","357"
> "2537","inflammatory and toxic neuropathy","icd9cm","357.9"
> "2537","inflammatory and toxic neuropathy","umls","C0154758"
> "2537","inflammatory and toxic neuropathy","mondo","0002336"
> "0111167","Dyggve-Melchior-Clausen disease","mondo","0009130"
> "0111166","molybdenum cofactor deficiency type C","mesh","C565374"
> "0111166","molybdenum cofactor deficiency type C","umls","C1854990"
> "0111166","molybdenum cofactor deficiency type C","mondo","0014212"
> "0050675","Birk-Barel syndrome","mesh","C567357"
> "0050675","Birk-Barel syndrome","mondo","0012856"
> "0050674","congenital bile acid synthesis defect","icd10cm","K76.8"
> "0050674","congenital bile acid synthesis defect","mondo","0018841"
> "0050677","Bjornstad syndrome","mondo","0009872"
> "0050676","Birt-Hogg-Dube syndrome","mesh","D058249"
> "0050676","Birt-Hogg-Dube syndrome","mondo","0007607"
> "0050670","ataxic cerebral palsy","mondo","0000397"
> "0050679","blue cone monochromacy","mondo","0010563"
> "0050678","Blau syndrome","mondo","0008523"
> "5078","ganglioglioma","mesh","D018303"
> "5078","ganglioglioma","umls","C0206716"
> "5078","ganglioglioma","umls","C1332202"
> "5078","ganglioglioma","umls","C1332969"
> "5078","ganglioglioma","mondo","0016733"
> "5076","mixed glioma","mesh","D005910"
> "5076","mixed glioma","umls","C0259783"
> "5076","mixed glioma","mondo","0003268"
> "5077","subependymal giant cell astrocytoma","mesh","D001254"
> "5077","subependymal giant cell astrocytoma","umls","C0205768"
> "5077","subependymal giant cell astrocytoma","mondo","0016693"
> "5074","malignant ependymoma","umls","C1333407"
> "5074","malignant ependymoma","mondo","0021191"
> "5075","myxopapillary ependymoma","mesh","D004806"
> "5075","myxopapillary ependymoma","umls","C0205769"
> "5075","myxopapillary ependymoma","mondo","0016699"
> "0111345","transient bullous dermolysis of the newborn","mesh","C536979"
> "0111345","transient bullous dermolysis of the newborn","umls","C1851573"
> "0111346","epidermolysis bullosa simplex with mottled pigmentation","mesh","C535959"
> "0111346","epidermolysis bullosa simplex with mottled pigmentation","umls","C0432316"
> "0111341","primary failure of tooth eruption","umls","C1852222"
> "0111340","dominant optic atrophy plus syndrome","umls","C3276549"
> "0111343","lateral meningocele syndrome","umls","C1851710"
> "0111342","dermatopathia pigmentosa reticularis","mesh","C535374"
> "0111342","dermatopathia pigmentosa reticularis","umls","C0406778"
> "0111349","hereditary desmoid disease","umls","C1851124"
> "0111348","multiple epiphyseal dysplasia with myopia and deafness","umls","C1851536"
> "0111329","pyridoxamine 5'-phosphate oxidase deficiency","umls","C1864723"
> "9561","nasopharyngeal disease","mesh","D009302"
> "9561","nasopharyngeal disease","umls","C0027438"
> "9561","nasopharyngeal disease","mondo","0004821"
> "9562","primary ciliary dyskinesia","mesh","D002925"
> "9562","primary ciliary dyskinesia","umls","C0008780"
> "9562","primary ciliary dyskinesia","mondo","0016575"
> "9563","bronchiectasis","icd10cm","J47"
> "9563","bronchiectasis","icd10cm","J47.9"
> "9563","bronchiectasis","icd9cm","494"
> "9563","bronchiectasis","mesh","D001987"
> "9563","bronchiectasis","umls","C0006267"
> "9563","bronchiectasis","mondo","0004822"
> "9565","dextrocardia","icd10cm","Q24.0"
> "9565","dextrocardia","mesh","D003914"
> "9565","dextrocardia","umls","C0011813"
> "9565","dextrocardia","mondo","0004823"
> "931","monieziasis","mesh","D008989"
> "931","monieziasis","umls","C0026414"
> "931","monieziasis","mondo","0004755"
> "930","orbital disease","icd10cm","H05"
> "930","orbital disease","icd10cm","H05.9"
> "930","orbital disease","icd9cm","376"
> "930","orbital disease","icd9cm","376.9"
> "930","orbital disease","mesh","D009916"
> "930","orbital disease","umls","C0029182"
> "930","orbital disease","mondo","0004751"
> "936","brain disease","icd10cm","G93.40"
> "936","brain disease","icd10cm","G93.9"
> "936","brain disease","icd9cm","348.3"
> "936","brain disease","icd9cm","348.30"
> "936","brain disease","icd9cm","348.9"
> "936","brain disease","mesh","D001927"
> "936","brain disease","umls","C0006111"
> "936","brain disease","umls","C0085584"
> "936","brain disease","mondo","0005560"
> "934","viral infectious disease","icd10cm","A94"
> "934","viral infectious disease","icd10cm","B34"
> "934","viral infectious disease","icd10cm","B34.9"
> "934","viral infectious disease","icd9cm","060-066.99"
> "934","viral infectious disease","icd9cm","066.9"
> "934","viral infectious disease","mesh","D001102"
> "934","viral infectious disease","mesh","D014777"
> "934","viral infectious disease","umls","C0003723"
> "934","viral infectious disease","umls","C0042769"
> "934","viral infectious disease","mondo","0005108"
> "5381","bile duct adenoma","mesh","D002759"
> "5381","bile duct adenoma","umls","C0008309"
> "5381","bile duct adenoma","mondo","0006108"
> "5382","Bartholin's gland adenoma","umls","C1511048"
> "5382","Bartholin's gland adenoma","mondo","0003419"
> "5384","bile duct cystadenoma","umls","C0334285"
> "5384","bile duct cystadenoma","mondo","0003420"
> "5385","mixed cell adenoma","umls","C0334323"
> "5385","mixed cell adenoma","mondo","0003421"
> "5386","lung adenoma","umls","C0345964"
> "5386","lung adenoma","mondo","0003422"
> "5387","middle ear adenoma","umls","C1334759"
> "5387","middle ear adenoma","mondo","0003423"
> "11836","clubfoot","icd10cm","Q66.0"
> "11836","clubfoot","icd10cm","Q66.89"
> "11836","clubfoot","icd9cm","754.51"
> "11836","clubfoot","mesh","D003025"
> "11836","clubfoot","umls","C0009081"
> "11836","clubfoot","mondo","0007342"
> "5389","oxyphilic adenoma","mesh","D018249"
> "5389","oxyphilic adenoma","umls","C1510502"
> "5389","oxyphilic adenoma","mondo","0003424"
> "11832","visual epilepsy","mesh","D012640"
> "11832","visual epilepsy","umls","C0270824"
> "11832","visual epilepsy","mondo","0001386"
> "11830","myopia","icd10cm","H52.1"
> "11830","myopia","icd9cm","367.1"
> "11830","myopia","mesh","D009216"
> "11830","myopia","umls","C0027092"
> "11830","myopia","mondo","0001384"
> "11831","cortical blindness","icd10cm","H47.61"
> "11831","cortical blindness","icd9cm","377.75"
> "11831","cortical blindness","mesh","D019575"
> "11831","cortical blindness","umls","C0155320"
> "11831","cortical blindness","mondo","0001385"
> "13098","central retinal artery occlusion","icd10cm","H34.1"
> "13098","central retinal artery occlusion","icd9cm","362.31"
> "13098","central retinal artery occlusion","mesh","D015356"
> "13098","central retinal artery occlusion","umls","C0007688"
> "13098","central retinal artery occlusion","mondo","0001633"
> "13099","Moyamoya disease","icd10cm","I67.5"
> "13099","Moyamoya disease","icd9cm","437.5"
> "13099","Moyamoya disease","mesh","D009072"
> "13099","Moyamoya disease","umls","C0026654"
> "13099","Moyamoya disease","mondo","0016820"
> "13096","Sneddon syndrome","mesh","D018860"
> "13096","Sneddon syndrome","umls","C0282492"
> "13096","Sneddon syndrome","mondo","0008436"
> "13097","intracranial arteriosclerosis","mesh","D002537"
> "13097","intracranial arteriosclerosis","umls","C0007771"
> "13097","intracranial arteriosclerosis","mondo","0001632"
> "13094","branch retinal artery occlusion","icd10cm","H34.23"
> "13094","branch retinal artery occlusion","icd9cm","362.32"
> "13094","branch retinal artery occlusion","mesh","D015356"
> "13094","branch retinal artery occlusion","umls","C0006123"
> "13094","branch retinal artery occlusion","mondo","0001630"
> "13095","vertebral artery insufficiency","mesh","D014715"
> "13095","vertebral artery insufficiency","umls","C0042560"
> "13095","vertebral artery insufficiency","mondo","0001631"
> "13580","cholestasis","icd10cm","K83.1"
> "13580","cholestasis","icd9cm","576.2"
> "13580","cholestasis","mesh","D002779"
> "13580","cholestasis","umls","C0008370"
> "13580","cholestasis","mondo","0001751"
> "9384","gonococcal iridocyclitis","icd10cm","A54.32"
> "9384","gonococcal iridocyclitis","icd9cm","098.41"
> "9384","gonococcal iridocyclitis","umls","C0153212"
> "9384","gonococcal iridocyclitis","mondo","0004774"
> "790","ocular hypotension","icd10cm","H44.4"
> "790","ocular hypotension","icd10cm","H44.40"
> "790","ocular hypotension","icd9cm","360.3"
> "790","ocular hypotension","icd9cm","360.30"
> "790","ocular hypotension","mesh","D015814"
> "790","ocular hypotension","umls","C0028841"
> "790","ocular hypotension","mondo","0004390"
> "0110540","autosomal recessive nonsyndromic deafness 98","icd10cm","H90.3"
> "0110540","autosomal recessive nonsyndromic deafness 98","mondo","0013929"
> "0110158","Charcot-Marie-Tooth disease type 2I","icd10cm","G60.0"
> "0110158","Charcot-Marie-Tooth disease type 2I","mondo","0011889"
> "9388","lens-induced iridocyclitis","icd10cm","H20.2"
> "9388","lens-induced iridocyclitis","icd9cm","364.23"
> "9388","lens-induced iridocyclitis","umls","C0339320"
> "9388","lens-induced iridocyclitis","mondo","0004775"
> "9389","infectious anterior uveitis","icd10cm","H20.03"
> "9389","infectious anterior uveitis","icd9cm","364.03"
> "9389","infectious anterior uveitis","umls","C0154911"
> "9389","infectious anterior uveitis","mondo","0017210"
> "799","varicose veins","icd10cm","I83.90"
> "799","varicose veins","mesh","D014648"
> "799","varicose veins","umls","C0042345"
> "799","varicose veins","mondo","0008638"
> "0110342","osteogenesis imperfecta type 13","icd10cm","Q78.0"
> "0110342","osteogenesis imperfecta type 13","mondo","0013924"
> "0110343","osteogenesis imperfecta type 14","icd10cm","Q78.0"
> "0110343","osteogenesis imperfecta type 14","mondo","0014029"
> "0110340","osteogenesis imperfecta type 4","icd10cm","Q78.0"
> "0110340","osteogenesis imperfecta type 4","mondo","0008148"
> "0110341","osteogenesis imperfecta type 2","icd10cm","Q78.0"
> "0110341","osteogenesis imperfecta type 2","mondo","0008147"
> "0110346","osteogenesis imperfecta type 10","icd10cm","Q78.0"
> "0110346","osteogenesis imperfecta type 10","mondo","0013459"
> "0110347","osteogenesis imperfecta type 15","icd10cm","Q78.0"
> "0110347","osteogenesis imperfecta type 15","mondo","0014086"
> "0110344","osteogenesis imperfecta type 5","icd10cm","Q78.0"
> "0110344","osteogenesis imperfecta type 5","mondo","0012591"
> "0110345","osteogenesis imperfecta type 16","icd10cm","Q78.0"
> "0110345","osteogenesis imperfecta type 16","mondo","0014544"
> "0110348","osteogenesis imperfecta type 12","icd10cm","Q78.0"
> "0110348","osteogenesis imperfecta type 12","mondo","0013460"
> "0110349","osteogenesis imperfecta type 9","icd10cm","Q78.0"
> "0110349","osteogenesis imperfecta type 9","mondo","0009805"
> "0110438","dilated cardiomyopathy 1JJ","icd10cm","I42.0"
> "0110438","dilated cardiomyopathy 1JJ","mondo","0014095"
> "0110439","dilated cardiomyopathy 1P","icd10cm","I42.0"
> "0110439","dilated cardiomyopathy 1P","mondo","0012362"
> "1138","spinal meningioma","mesh","D008579"
> "1138","spinal meningioma","umls","C0347515"
> "1138","spinal meningioma","mondo","0001275"
> "0110541","autosomal dominant nonsyndromic deafness 1","icd10cm","H90.3"
> "0110541","autosomal dominant nonsyndromic deafness 1","mondo","0007424"
> "1130","pituitary infarct","umls","C0342405"
> "1130","pituitary infarct","mondo","0001259"
> "1134","gingival recession","icd10cm","K06.0"
> "1134","gingival recession","icd10cm","K06.01"
> "1134","gingival recession","icd10cm","K06.010"
> "1134","gingival recession","icd9cm","523.2"
> "1134","gingival recession","icd9cm","523.20"
> "1134","gingival recession","icd9cm","523.24"
> "1134","gingival recession","mesh","D005889"
> "1134","gingival recession","umls","C0017572"
> "1134","gingival recession","umls","C0266916"
> "1134","gingival recession","mondo","0001268"
> "10790","chronic frontal sinusitis","icd10cm","J32.1"
> "10790","chronic frontal sinusitis","icd9cm","473.1"
> "10790","chronic frontal sinusitis","umls","C0008683"
> "10790","chronic frontal sinusitis","mondo","0001120"
> "13777","epidermodysplasia verruciformis","mesh","D004819"
> "13777","epidermodysplasia verruciformis","umls","C0014522"
> "13777","epidermodysplasia verruciformis","mondo","0009176"
> "0060276","pontocerebellar hypoplasia type 7","icd10cm","Q04.3"
> "0060276","pontocerebellar hypoplasia type 7","mondo","0013993"
> "0060277","pontocerebellar hypoplasia type 8","icd10cm","Q04.3"
> "0060277","pontocerebellar hypoplasia type 8","mondo","0013990"
> "0060274","pontocerebellar hypoplasia type 5","mesh","C537745"
> "0060274","pontocerebellar hypoplasia type 5","umls","C1857762"
> "0060274","pontocerebellar hypoplasia type 5","mondo","0012438"
> "0060275","pontocerebellar hypoplasia type 6","mesh","C548074"
> "0060275","pontocerebellar hypoplasia type 6","umls","C1969084"
> "0060275","pontocerebellar hypoplasia type 6","mondo","0012683"
> "7148","rheumatoid arthritis","kegg","05323"
> "7148","rheumatoid arthritis","icd10cm","M06.9"
> "7148","rheumatoid arthritis","icd9cm","714.0"
> "7148","rheumatoid arthritis","mesh","D001172"
> "7148","rheumatoid arthritis","umls","C0003873"
> "7148","rheumatoid arthritis","mondo","0008383"
> "0060273","pontocerebellar hypoplasia type 4","mesh","C536716"
> "0060273","pontocerebellar hypoplasia type 4","umls","C1856974"
> "0060273","pontocerebellar hypoplasia type 4","mondo","0009166"
> "0060270","pontocerebellar hypoplasia type 2D","icd10cm","Q04.3"
> "0060270","pontocerebellar hypoplasia type 2D","mondo","0013438"
> "0060271","pontocerebellar hypoplasia type 2E","mondo","0014370"
> "7144","laryngeal small cell carcinoma","umls","C1334378"
> "7144","laryngeal small cell carcinoma","mondo","0006265"
> "7146","Langerhans cell sarcoma","icd10cm","C96.4"
> "7146","Langerhans cell sarcoma","mesh","D054752"
> "7146","Langerhans cell sarcoma","umls","C1260327"
> "7146","Langerhans cell sarcoma","mondo","0019480"
> "7147","ankylosing spondylitis","icd10cm","M45"
> "7147","ankylosing spondylitis","icd9cm","720.0"
> "7147","ankylosing spondylitis","mesh","D013167"
> "7147","ankylosing spondylitis","umls","C0038013"
> "7147","ankylosing spondylitis","mondo","0005306"
> "7140","Bartholin's gland small cell carcinoma","umls","C1511051"
> "7140","Bartholin's gland small cell carcinoma","mondo","0004120"
> "7141","prostate small cell carcinoma","umls","C1300585"
> "7141","prostate small cell carcinoma","mondo","0006390"
> "7142","thymus small cell carcinoma","umls","C1335980"
> "7142","thymus small cell carcinoma","mondo","0004122"
> "0060279","pontocerebellar hypoplasia type 10","mondo","0014349"
> "2149","urogenital tuberculosis","icd10cm","A18.1"
> "2149","urogenital tuberculosis","icd10cm","A18.10"
> "2149","urogenital tuberculosis","icd9cm","016"
> "2149","urogenital tuberculosis","icd9cm","016.9"
> "2149","urogenital tuberculosis","mesh","D014401"
> "2149","urogenital tuberculosis","umls","C0041333"
> "2149","urogenital tuberculosis","mondo","0006002"
> "8501","fundus dystrophy","mesh","D058499"
> "8501","fundus dystrophy","umls","C0854723"
> "8501","fundus dystrophy","mondo","0019118"
> "8500","hereditary retinal dystrophy","icd10cm","H35.5"
> "8500","hereditary retinal dystrophy","icd10cm","H35.50"
> "8500","hereditary retinal dystrophy","icd9cm","362.7"
> "8500","hereditary retinal dystrophy","icd9cm","362.70"
> "8500","hereditary retinal dystrophy","umls","C0154860"
> "8500","hereditary retinal dystrophy","mondo","0019118"
> "8503","impetigo herpetiformis","icd10cm","L40.1"
> "8503","impetigo herpetiformis","icd9cm","694.3"
> "8503","impetigo herpetiformis","umls","C1314968"
> "8503","impetigo herpetiformis","mondo","0004591"
> "8050","bladder tubulo-cystic clear cell adenocarcinoma","umls","C1511203"
> "8050","bladder tubulo-cystic clear cell adenocarcinoma","mondo","0004444"
> "8057","olfactory groove meningioma","mesh","D008579"
> "8057","olfactory groove meningioma","umls","C1335107"
> "8057","olfactory groove meningioma","mondo","0004446"
> "8504","impetigo","icd10cm","L01"
> "8504","impetigo","icd10cm","L01.0"
> "8504","impetigo","icd10cm","L01.00"
> "8504","impetigo","icd9cm","684"
> "8504","impetigo","mesh","D007169"
> "8504","impetigo","umls","C0021099"
> "8504","impetigo","mondo","0004592"
> "8507","juvenile dermatitis herpetiformis","icd10cm","L12.2"
> "8507","juvenile dermatitis herpetiformis","icd9cm","694.2"
> "8507","juvenile dermatitis herpetiformis","umls","C0152092"
> "8507","juvenile dermatitis herpetiformis","mondo","0006565"
> "8506","bullous pemphigoid","icd10cm","L12"
> "8506","bullous pemphigoid","icd10cm","L12.0"
> "8506","bullous pemphigoid","icd10cm","L12.9"
> "8506","bullous pemphigoid","icd9cm","694.5"
> "8506","bullous pemphigoid","mesh","D010391"
> "8506","bullous pemphigoid","umls","C0030805"
> "8506","bullous pemphigoid","mondo","0019082"
> "8508","subcorneal pustular dermatosis","icd10cm","L13.1"
> "8508","subcorneal pustular dermatosis","icd9cm","694.1"
> "8508","subcorneal pustular dermatosis","mesh","D012872"
> "8508","subcorneal pustular dermatosis","umls","C0600336"
> "8508","subcorneal pustular dermatosis","mondo","0006614"
> "8058","pituitary stalk meningioma","umls","C1335422"
> "8058","pituitary stalk meningioma","mondo","0004447"
> "13585","alveolar periostitis","icd10cm","M27.3"
> "13585","alveolar periostitis","icd9cm","526.5"
> "13585","alveolar periostitis","mesh","D004368"
> "13585","alveolar periostitis","umls","C0013240"
> "13585","alveolar periostitis","mondo","0001752"
> "2883","prostatic adenoma","mesh","D011470"
> "2883","prostatic adenoma","umls","C0520477"
> "2883","prostatic adenoma","mondo","0002450"
> "2887","prostate leiomyoma","umls","C1335510"
> "2887","prostate leiomyoma","mondo","0002452"
> "222","perichondritis of auricle","icd10cm","H61.0"
> "222","perichondritis of auricle","icd10cm","H61.00"
> "222","perichondritis of auricle","icd10cm","H61.009"
> "222","perichondritis of auricle","icd9cm","380.0"
> "222","perichondritis of auricle","icd9cm","380.00"
> "222","perichondritis of auricle","umls","C0155389"
> "222","perichondritis of auricle","mondo","0002246"
> "0060055","popliteal pterygium syndrome","mesh","C562509"
> "0060055","popliteal pterygium syndrome","umls","C0265259"
> "0060055","popliteal pterygium syndrome","mondo","0017435"
> "7492","central epithelioid sarcoma","umls","C1335563"
> "7492","central epithelioid sarcoma","mondo","0004244"
> "0060058","lymphoma","icd10cm","C85.9"
> "0060058","lymphoma","mesh","D008223"
> "0060058","lymphoma","umls","C0024299"
> "0060058","lymphoma","umls","C0598798"
> "0060058","lymphoma","mondo","0005062"
> "7491","vulvar proximal-type epithelioid sarcoma","umls","C1520093"
> "7491","vulvar proximal-type epithelioid sarcoma","mondo","0004243"
> "7497","brain ependymoma","umls","C0238029"
> "7497","brain ependymoma","mondo","0004245"
> "0080038","pycnodysostosis","mesh","D058631"
> "0080038","pycnodysostosis","mondo","0009940"
> "13389","labia majora carcinoma","umls","C1334356"
> "13389","labia majora carcinoma","mondo","0001702"
> "1921","Klinefelter's syndrome","icd10cm","Q98.0"
> "1921","Klinefelter's syndrome","icd10cm","Q98.4"
> "1921","Klinefelter's syndrome","icd9cm","758.7"
> "1921","Klinefelter's syndrome","mesh","D007713"
> "1921","Klinefelter's syndrome","umls","C0022735"
> "1921","Klinefelter's syndrome","mondo","0006823"
> "3274","proliferative type fibrocystic change of breast","umls","C0334056"
> "3274","proliferative type fibrocystic change of breast","mondo","0002585"
> "1923","sex development disorder","mesh","D012734"
> "1923","sex development disorder","umls","C0036875"
> "1923","sex development disorder","mondo","0002145"
> "0080218","primary spontaneous pneumothorax","mondo","0008259"
> "0080219","dystransthyretinemic hyperthyroxinemia","mondo","0007785"
> "3602","toxic encephalopathy","mesh","D020258"
> "3602","toxic encephalopathy","umls","C0235032"
> "3602","toxic encephalopathy","mondo","0005527"
> "0080212","polycystic kidney disease 4","mondo","0033004"
> "0080213","punctate palmoplantar keratoderma type II","mondo","0008292"
> "0080210","primary mediastinal B-cell lymphoma","icd10cm","C85.2"
> "0080210","primary mediastinal B-cell lymphoma","mondo","0020323"
> "0080211","nodal marginal zone lymphoma","mondo","0019465"
> "0080216","duodenal atresia","mesh","C535720"
> "0080216","duodenal atresia","mondo","0009126"
> "0080041","hypochondroplasia","icd10cm","Q77.4"
> "0080041","hypochondroplasia","mesh","C562937"
> "0080041","hypochondroplasia","umls","C0410529"
> "0080041","hypochondroplasia","mondo","0007793"
> "0080214","punctate palmoplantar keratoderma type 1A","mondo","0007858"
> "0080215","early infantile epileptic encephalopathy 8","mondo","0010375"
> "13589","female infertility of uterine origin","icd10cm","N97.2"
> "13589","female infertility of uterine origin","icd9cm","628.3"
> "13589","female infertility of uterine origin","umls","C0156416"
> "13589","female infertility of uterine origin","mondo","0001753"
> "4762","vasculogenic impotence","mesh","D018783"
> "4762","vasculogenic impotence","umls","C0243000"
> "4762","vasculogenic impotence","mondo","0007013"
> "4765","pulmonary blastoma","mesh","D018202"
> "4765","pulmonary blastoma","umls","C0206629"
> "4765","pulmonary blastoma","mondo","0005933"
> "13655","acquired tear duct stenosis","icd10cm","H04.55"
> "13655","acquired tear duct stenosis","icd9cm","375.56"
> "13655","acquired tear duct stenosis","umls","C0155248"
> "13655","acquired tear duct stenosis","mondo","0001769"
> "4767","classic pulmonary blastoma","umls","C1332556"
> "4767","classic pulmonary blastoma","mondo","0003128"
> "4766","embryoma","umls","C0936282"
> "4766","embryoma","mondo","0003127"
> "4769","pleuropulmonary blastoma","mesh","C537516"
> "4769","pleuropulmonary blastoma","umls","C1266144"
> "4769","pleuropulmonary blastoma","mondo","0011014"
> "4768","epithelial predominant pulmonary blastoma","umls","C1333420"
> "4768","epithelial predominant pulmonary blastoma","mondo","0003129"
> "11249","vitamin K deficiency bleeding","icd10cm","E56.1"
> "11249","vitamin K deficiency bleeding","icd9cm","269.0"
> "11249","vitamin K deficiency bleeding","mesh","D014813"
> "11249","vitamin K deficiency bleeding","umls","C0042880"
> "11249","vitamin K deficiency bleeding","mondo","0001244"
> "3605","ovarian cystadenocarcinoma","umls","C1096638"
> "3605","ovarian cystadenocarcinoma","mondo","0002702"
> "11245","transient neonatal neutropenia","icd10cm","P61.5"
> "11245","transient neonatal neutropenia","icd9cm","776.7"
> "11245","transient neonatal neutropenia","umls","C0158997"
> "11245","transient neonatal neutropenia","mondo","0001241"
> "11244","neonatal anemia","mesh","D000751"
> "11244","neonatal anemia","umls","C0002891"
> "11244","neonatal anemia","mondo","0001240"
> "11247","disseminated intravascular coagulation","icd10cm","D65"
> "11247","disseminated intravascular coagulation","icd9cm","286.6"
> "11247","disseminated intravascular coagulation","mesh","D004211"
> "11247","disseminated intravascular coagulation","umls","C0012739"
> "11247","disseminated intravascular coagulation","mondo","0001243"
> "3604","ovarian mucinous cystadenocarcinoma","umls","C0279665"
> "3604","ovarian mucinous cystadenocarcinoma","mondo","0002701"
> "11241","appendix lymphoma","umls","C1332328"
> "11241","appendix lymphoma","mondo","0001237"
> "11240","appendiceal neoplasm","mesh","D001063"
> "11240","appendiceal neoplasm","umls","C0003614"
> "11240","appendiceal neoplasm","mondo","0001236"
> "11243","anemia of prematurity","icd10cm","P61.2"
> "11243","anemia of prematurity","icd9cm","776.6"
> "11243","anemia of prematurity","umls","C0158996"
> "11243","anemia of prematurity","mondo","0001239"
> "11242","plethora of newborn","icd10cm","P61.1"
> "11242","plethora of newborn","icd9cm","776.4"
> "11242","plethora of newborn","umls","C0272153"
> "11242","plethora of newborn","mondo","0001238"
> "5809","childhood parosteal osteogenic sarcoma","umls","C1332994"
> "5809","childhood parosteal osteogenic sarcoma","mondo","0003654"
> "5806","stork bite","mondo","0003653"
> "5805","subvalvular aortic stenosis","mesh","D001020"
> "5805","subvalvular aortic stenosis","umls","C0340375"
> "5805","subvalvular aortic stenosis","mondo","0006987"
> "5804","discrete subaortic stenosis","mesh","D021922"
> "5804","discrete subaortic stenosis","umls","C0012628"
> "5804","discrete subaortic stenosis","mondo","0006729"
> "0110535","autosomal recessive nonsyndromic deafness 9","icd10cm","H90.3"
> "0110535","autosomal recessive nonsyndromic deafness 9","mondo","0010986"
> "0110534","autosomal recessive nonsyndromic deafness 89","icd10cm","H90.3"
> "0110534","autosomal recessive nonsyndromic deafness 89","mondo","0013489"
> "1572","normal pressure hydrocephalus","icd10cm","G91.2"
> "1572","normal pressure hydrocephalus","mesh","D006850"
> "1572","normal pressure hydrocephalus","umls","C0020258"
> "1572","normal pressure hydrocephalus","mondo","0009366"
> "1571","spastic ectropion","icd9cm","374.13"
> "1571","spastic ectropion","umls","C0155195"
> "1571","spastic ectropion","mondo","0002044"
> "1570","ectropion","icd10cm","H02.1"
> "1570","ectropion","icd10cm","H02.10"
> "1570","ectropion","icd10cm","H02.109"
> "1570","ectropion","icd9cm","374.1"
> "1570","ectropion","icd9cm","374.10"
> "1570","ectropion","mesh","D004483"
> "1570","ectropion","umls","C0013592"
> "1570","ectropion","mondo","0002043"
> "11793","phthisical cornea","icd9cm","371.05"
> "11793","phthisical cornea","umls","C0155102"
> "11793","phthisical cornea","mondo","0001368"
> "1577","limited scleroderma","mesh","D045745"
> "1577","limited scleroderma","umls","C0748540"
> "1577","limited scleroderma","mondo","0006832"
> "11797","chronic laryngitis","icd10cm","J37.0"
> "11797","chronic laryngitis","icd9cm","476.0"
> "11797","chronic laryngitis","umls","C0155836"
> "11797","chronic laryngitis","mondo","0001369"
> "0070220","familial hyperinsulinemic hypoglycemia 5","mondo","0012381"
> "1826","epilepsy","icd10cm","G40.9"
> "1826","epilepsy","icd10cm","G40.909"
> "1826","epilepsy","icd9cm","345.9"
> "1826","epilepsy","mesh","D004827"
> "1826","epilepsy","umls","C0014544"
> "1826","epilepsy","mondo","0005027"
> "1574","alcohol use disorder","icd10cm","F10.1"
> "1574","alcohol use disorder","icd9cm","305.0"
> "1574","alcohol use disorder","icd9cm","305.00"
> "1574","alcohol use disorder","mesh","D000437"
> "1574","alcohol use disorder","umls","C0085762"
> "1574","alcohol use disorder","mondo","0002046"
> "0070223","progressive familial intrahepatic cholestasis 3","mesh","C535935"
> "0070223","progressive familial intrahepatic cholestasis 3","umls","C1865643"
> "0070223","progressive familial intrahepatic cholestasis 3","mondo","0011214"
> "0110539","autosomal recessive nonsyndromic deafness 97","icd10cm","H90.3"
> "0110539","autosomal recessive nonsyndromic deafness 97","mondo","0014739"
> "0070225","progressive familial intrahepatic cholestasis 5","mondo","0014884"
> "11990","ulceroglandular tularemia","icd10cm","A21.0"
> "11990","ulceroglandular tularemia","icd9cm","021.0"
> "11990","ulceroglandular tularemia","umls","C0152941"
> "11990","ulceroglandular tularemia","mondo","0001413"
> "0050083","Keshan disease","mondo","0000241"
> "10354","breast fibrocystic disease","icd10cm","N60"
> "10354","breast fibrocystic disease","icd10cm","N60.1"
> "10354","breast fibrocystic disease","icd9cm","610.1"
> "10354","breast fibrocystic disease","mesh","D005348"
> "10354","breast fibrocystic disease","umls","C0016034"
> "10354","breast fibrocystic disease","mondo","0005219"
> "4889","lymph node tuberculosis","icd10cm","A18.2"
> "4889","lymph node tuberculosis","mesh","D014388"
> "4889","lymph node tuberculosis","mesh","D018601"
> "4889","lymph node tuberculosis","umls","C0041316"
> "4889","lymph node tuberculosis","umls","C0242830"
> "4889","lymph node tuberculosis","mondo","0005831"
> "10350","breast cyst","icd10cm","N60.0"
> "10350","breast cyst","mesh","D047688"
> "10350","breast cyst","umls","C0006144"
> "10350","breast cyst","mondo","0001011"
> "2708","mushroom workers' lung","icd10cm","J67.5"
> "2708","mushroom workers' lung","icd9cm","495.5"
> "2708","mushroom workers' lung","mesh","D005203"
> "2708","mushroom workers' lung","umls","C0155889"
> "2708","mushroom workers' lung","mondo","0005865"
> "10352","breast fibroadenosis","icd10cm","N60.2"
> "10352","breast fibroadenosis","icd9cm","610.2"
> "10352","breast fibroadenosis","umls","C1305875"
> "10352","breast fibroadenosis","mondo","0001012"
> "10353","fibrosclerosis of breast","icd10cm","N60.3"
> "10353","fibrosclerosis of breast","icd9cm","610.3"
> "10353","fibrosclerosis of breast","umls","C0156318"
> "10353","fibrosclerosis of breast","mondo","0006118"
> "4880","kidney clear cell sarcoma","umls","C0334488"
> "4880","kidney clear cell sarcoma","mondo","0005006"
> "2704","malignant giant cell tumor of the tendon sheath","umls","C1266168"
> "2704","malignant giant cell tumor of the tendon sheath","mondo","0002401"
> "2706","synovium cancer","umls","C1334624"
> "2706","synovium cancer","mondo","0002403"
> "2701","nodular tenosynovitis","mesh","D000070779"
> "2701","nodular tenosynovitis","umls","C0221289"
> "2701","nodular tenosynovitis","umls","C0588125"
> "2701","nodular tenosynovitis","mondo","0002399"
> "4885","Colorado tick fever","icd10cm","A93.2"
> "4885","Colorado tick fever","mesh","D003121"
> "4885","Colorado tick fever","umls","C0009400"
> "4885","Colorado tick fever","mondo","0005708"
> "2703","synovitis","mesh","D013585"
> "2703","synovitis","umls","C0039103"
> "2703","synovitis","mondo","0002400"
> "2702","pigmented villonodular synovitis","icd10cm","M12.2"
> "2702","pigmented villonodular synovitis","mesh","D013586"
> "2702","pigmented villonodular synovitis","umls","C0039106"
> "2702","pigmented villonodular synovitis","mondo","0006906"
> "7962","tamoxifen-related endometrial lesion","umls","C1515212"
> "7962","tamoxifen-related endometrial lesion","mondo","0004414"
> "7960","malignant spiradenoma","umls","C1266063"
> "7960","malignant spiradenoma","mondo","0004412"
> "7961","cervical non-keratinizing squamous cell carcinoma","umls","C1518366"
> "7961","cervical non-keratinizing squamous cell carcinoma","mondo","0004413"
> "0070138","autosomal recessive cutis laxa type IIIB","icd10cm","Q82.8"
> "0070138","autosomal recessive cutis laxa type IIIB","mondo","0013755"
> "0070139","autosomal recessive cutis laxa type IC","mesh","C567716"
> "0070139","autosomal recessive cutis laxa type IC","umls","C2750804"
> "0070139","autosomal recessive cutis laxa type IC","mondo","0013170"
> "0070134","autosomal recessive cutis laxa type IIA","icd10cm","Q82.8"
> "0070134","autosomal recessive cutis laxa type IIA","mondo","0018163"
> "0070135","autosomal recessive cutis laxa type IA","icd10cm","Q82.8"
> "0070135","autosomal recessive cutis laxa type IA","mondo","0009052"
> "7968","plasmacytoid variant infiltrating bladder urothelial carcinoma","umls","C1512742"
> "7968","plasmacytoid variant infiltrating bladder urothelial carcinoma","mondo","0004416"
> "9174","rectum carcinoma in situ","icd10cm","D01.2"
> "9174","rectum carcinoma in situ","icd9cm","230.4"
> "9174","rectum carcinoma in situ","umls","C0154062"
> "9174","rectum carcinoma in situ","mondo","0004725"
> "0070130","autosomal dominant cutis laxa 1","icd10cm","Q82.8"
> "0070130","autosomal dominant cutis laxa 1","mondo","0007411"
> "0070131","autosomal dominant cutis laxa 3","icd10cm","Q82.8"
> "0070131","autosomal dominant cutis laxa 3","mondo","0014706"
> "0070132","autosomal recessive cutis laxa type IIIA","icd10cm","Q82.8"
> "0070132","autosomal recessive cutis laxa type IIIA","mondo","0009053"
> "0070133","autosomal recessive cutis laxa type IB","icd10cm","Q82.8"
> "0070133","autosomal recessive cutis laxa type IB","mondo","0013754"
> "6259","type 2 papillary adenoma of the kidney","umls","C1519710"
> "6259","type 2 papillary adenoma of the kidney","mondo","0003831"
> "6258","type 1 papillary adenoma of the kidney","umls","C1519706"
> "6258","type 1 papillary adenoma of the kidney","mondo","0003830"
> "0111592","plasminogen deficiency type I","mesh","C566897"
> "0111592","plasminogen deficiency type I","mesh","C580017"
> "0111592","plasminogen deficiency type I","umls","C0398621"
> "0111592","plasminogen deficiency type I","umls","C1968804"
> "12837","thyroid crisis","mesh","D013958"
> "12837","thyroid crisis","umls","C0040127"
> "12837","thyroid crisis","mondo","0006996"
> "0050657","Bannayan-Riley-Ruvalcaba syndrome","icd10cm","Q87.89"
> "0050657","Bannayan-Riley-Ruvalcaba syndrome","mesh","D006223"
> "0050657","Bannayan-Riley-Ruvalcaba syndrome","mondo","0007924"
> "6257","chromophil adenoma of the kidney","umls","C1518879"
> "6257","chromophil adenoma of the kidney","mondo","0003829"
> "6256","malignant growth hormone secreting neoplasm of pituitary","umls","C1334587"
> "6256","malignant growth hormone secreting neoplasm of pituitary","mondo","0003828"
> "6255","growth hormone secreting pituitary adenoma","mesh","D049912"
> "6255","growth hormone secreting pituitary adenoma","umls","C0346302"
> "6255","growth hormone secreting pituitary adenoma","mondo","0006238"
> "12265","chronic salpingo-oophoritis","icd10cm","N70.1"
> "12265","chronic salpingo-oophoritis","icd10cm","N70.13"
> "12265","chronic salpingo-oophoritis","icd9cm","614.1"
> "12265","chronic salpingo-oophoritis","umls","C0156328"
> "12265","chronic salpingo-oophoritis","mondo","0001474"
> "10533","viral pneumonia","icd10cm","J12.9"
> "10533","viral pneumonia","icd9cm","480"
> "10533","viral pneumonia","icd9cm","480.9"
> "10533","viral pneumonia","mesh","D011024"
> "10533","viral pneumonia","umls","C0032310"
> "10533","viral pneumonia","mondo","0006012"
> "10534","stomach cancer","icd10cm","C16"
> "10534","stomach cancer","icd10cm","C16.2"
> "10534","stomach cancer","icd10cm","C16.5"
> "10534","stomach cancer","icd10cm","C16.6"
> "10534","stomach cancer","icd10cm","C16.9"
> "10534","stomach cancer","icd9cm","151"
> "10534","stomach cancer","icd9cm","151.4"
> "10534","stomach cancer","icd9cm","151.5"
> "10534","stomach cancer","icd9cm","151.6"
> "10534","stomach cancer","icd9cm","151.9"
> "10534","stomach cancer","mesh","D013274"
> "10534","stomach cancer","umls","C0024623"
> "10534","stomach cancer","umls","C0038356"
> "10534","stomach cancer","umls","C0153421"
> "10534","stomach cancer","umls","C0153422"
> "10534","stomach cancer","umls","C0153423"
> "10534","stomach cancer","mondo","0001056"
> "10536","malignant gastric granular cell tumor","umls","C1334585"
> "10536","malignant gastric granular cell tumor","mondo","0001057"
> "10538","gastric fundus cancer","icd10cm","C16.1"
> "10538","gastric fundus cancer","icd9cm","151.3"
> "10538","gastric fundus cancer","umls","C0153420"
> "10538","gastric fundus cancer","mondo","0001058"
> "9719","neovascular inflammatory vitreoretinopathy","mesh","D018630"
> "9719","neovascular inflammatory vitreoretinopathy","umls","C0242852"
> "9719","neovascular inflammatory vitreoretinopathy","mondo","0006928"
> "0110248","cataract 30","icd10cm","Q12.0"
> "0110248","cataract 30","mondo","0007286"
> "2517","intracranial structure hemangioma","icd10cm","D18.02"
> "2517","intracranial structure hemangioma","icd9cm","228.02"
> "2517","intracranial structure hemangioma","umls","C0154050"
> "2517","intracranial structure hemangioma","mondo","0002328"
> "9717","hydrops of gallbladder","icd10cm","K82.1"
> "9717","hydrops of gallbladder","icd9cm","575.3"
> "9717","hydrops of gallbladder","umls","C0152445"
> "9717","hydrops of gallbladder","mondo","0004859"
> "9714","occlusion of gallbladder","icd10cm","K82.0"
> "9714","occlusion of gallbladder","icd9cm","575.2"
> "9714","occlusion of gallbladder","umls","C0156214"
> "9714","occlusion of gallbladder","mondo","0004858"
> "833","auditory system cancer","mesh","D004428"
> "833","auditory system cancer","umls","C0013449"
> "833","auditory system cancer","mondo","0004532"
> "2410","skin granular cell tumor","umls","C0346060"
> "2410","skin granular cell tumor","mondo","0002291"
> "8541","Sezary's disease","icd10cm","C84.1"
> "8541","Sezary's disease","icd10cm","C84.10"
> "8541","Sezary's disease","icd9cm","202.2"
> "8541","Sezary's disease","mesh","D012751"
> "8541","Sezary's disease","umls","C0036920"
> "8541","Sezary's disease","mondo","0017844"
> "8886","chorioretinitis","icd10cm","H30"
> "8886","chorioretinitis","icd10cm","H30.9"
> "8886","chorioretinitis","icd9cm","363.20"
> "8886","chorioretinitis","mesh","D002825"
> "8886","chorioretinitis","umls","C0008513"
> "8886","chorioretinitis","mondo","0004674"
> "3478","iris cancer","mesh","D015811"
> "3478","iris cancer","umls","C0022079"
> "3478","iris cancer","umls","C0346372"
> "3478","iris cancer","mondo","0002658"
> "3479","uveal cancer","mesh","D014604"
> "3479","uveal cancer","umls","C0042162"
> "3479","uveal cancer","umls","C1334629"
> "3479","uveal cancer","mondo","0002659"
> "8883","lower lip cancer","icd10cm","C00.1"
> "8883","lower lip cancer","icd9cm","140.1"
> "8883","lower lip cancer","umls","C0432520"
> "8883","lower lip cancer","mondo","0004673"
> "11289","ventilation pneumonitis","icd10cm","J67.7"
> "11289","ventilation pneumonitis","icd9cm","495.7"
> "11289","ventilation pneumonitis","umls","C0155891"
> "11289","ventilation pneumonitis","mondo","0001255"
> "0111394","mucopolysaccharidosis type IIIB","umls","C0086648"
> "14239","gastrointestinal tularemia","icd9cm","021.1"
> "14239","gastrointestinal tularemia","icd9cm","021.8"
> "14239","gastrointestinal tularemia","umls","C0029835"
> "14239","gastrointestinal tularemia","umls","C0152942"
> "14239","gastrointestinal tularemia","mondo","0001916"
> "1729","retinal vascular occlusion","icd10cm","H34"
> "1729","retinal vascular occlusion","icd10cm","H34.9"
> "1729","retinal vascular occlusion","icd9cm","362.3"
> "1729","retinal vascular occlusion","icd9cm","362.30"
> "1729","retinal vascular occlusion","umls","C0035326"
> "1729","retinal vascular occlusion","mondo","0002089"
> "1726","partial of retinal vein occlusion","icd10cm","H34.82"
> "1726","partial of retinal vein occlusion","umls","C0271080"
> "1726","partial of retinal vein occlusion","mondo","0002088"
> "0040046","nickel allergic contact dermatitis","icd10cm","L23.0"
> "1724","duodenal ulcer","icd10cm","K26"
> "1724","duodenal ulcer","icd9cm","532"
> "1724","duodenal ulcer","mesh","D004381"
> "1724","duodenal ulcer","umls","C0010474"
> "1724","duodenal ulcer","umls","C0013295"
> "1724","duodenal ulcer","mondo","0005412"
> "1725","peritoneum cancer","icd10cm","C48.1"
> "1725","peritoneum cancer","icd9cm","158.8"
> "1725","peritoneum cancer","umls","C0153466"
> "1725","peritoneum cancer","mondo","0002087"
> "5241","hemangioblastoma","mesh","D018325"
> "5241","hemangioblastoma","umls","C0206734"
> "5241","hemangioblastoma","mondo","0016748"
> "5240","retinal hemangioblastoma","umls","C1514915"
> "5240","retinal hemangioblastoma","mondo","0003343"
> "13135","exophthalmic ophthalmoplegia","icd9cm","376.22"
> "13135","exophthalmic ophthalmoplegia","umls","C0152135"
> "13135","exophthalmic ophthalmoplegia","mondo","0001643"
> "13134","hordeolum externum","icd10cm","H00.01"
> "13134","hordeolum externum","icd10cm","H00.03"
> "13134","hordeolum externum","icd9cm","373.11"
> "13134","hordeolum externum","umls","C0019919"
> "13134","hordeolum externum","mondo","0001642"
> "13137","Werdnig-Hoffmann disease","icd10cm","G12.0"
> "13137","Werdnig-Hoffmann disease","icd9cm","335.0"
> "13137","Werdnig-Hoffmann disease","mesh","D014897"
> "13137","Werdnig-Hoffmann disease","umls","C0043116"
> "13137","Werdnig-Hoffmann disease","mondo","0009669"
> "13133","HELLP syndrome","icd10cm","O14.2"
> "13133","HELLP syndrome","mesh","D017359"
> "13133","HELLP syndrome","umls","C0162739"
> "13133","HELLP syndrome","mondo","0008585"
> "13139","crescentic glomerulonephritis","umls","C0403416"
> "13139","crescentic glomerulonephritis","mondo","0001645"
> "13138","acute proliferative glomerulonephritis","icd9cm","580.0"
> "13138","acute proliferative glomerulonephritis","umls","C0341692"
> "13138","acute proliferative glomerulonephritis","mondo","0001644"
> "3004","breast myoepithelial neoplasm","umls","C1511319"
> "3004","breast myoepithelial neoplasm","mondo","0002483"
> "3007","breast ductal carcinoma","mesh","D044584"
> "3007","breast ductal carcinoma","umls","C1176475"
> "3007","breast ductal carcinoma","mondo","0005590"
> "3001","female reproductive endometrioid cancer","umls","C0474809"
> "3001","female reproductive endometrioid cancer","mondo","0002480"
> "3003","nipple neoplasm","umls","C1112166"
> "3003","nipple neoplasm","mondo","0002482"
> "3002","ovary neuroendocrine neoplasm","umls","C1335172"
> "3002","ovary neuroendocrine neoplasm","mondo","0002481"
> "14308","skin epithelioid hemangioma","mesh","D000796"
> "14308","skin epithelioid hemangioma","umls","C0002989"
> "14308","skin epithelioid hemangioma","mondo","0001939"
> "3009","breast neuroendocrine neoplasm","umls","C1332635"
> "3009","breast neuroendocrine neoplasm","mondo","0002485"
> "3008","invasive ductal carcinoma","mesh","D018270"
> "3008","invasive ductal carcinoma","umls","C1134719"
> "3008","invasive ductal carcinoma","umls","C1527349"
> "3008","invasive ductal carcinoma","mondo","0004953"
> "9459","isthmus cancer","icd9cm","182.1"
> "9459","isthmus cancer","umls","C0153575"
> "9459","isthmus cancer","mondo","0004792"
> "1588","thrombocytopenia","icd10cm","D69.6"
> "1588","thrombocytopenia","icd9cm","287.5"
> "1588","thrombocytopenia","mesh","D013921"
> "1588","thrombocytopenia","umls","C0040034"
> "1588","thrombocytopenia","mondo","0002049"
> "5484","fibrous synovial sarcoma","umls","C1333616"
> "5484","fibrous synovial sarcoma","mondo","0003465"
> "1583","laryngeal tuberculosis","icd10cm","A15.5"
> "1583","laryngeal tuberculosis","icd9cm","012.3"
> "1583","laryngeal tuberculosis","mesh","D014387"
> "1583","laryngeal tuberculosis","umls","C0041315"
> "1583","laryngeal tuberculosis","mondo","0005819"
> "1580","diffuse scleroderma","mesh","D045743"
> "1580","diffuse scleroderma","umls","C1258104"
> "1580","diffuse scleroderma","mondo","0005019"
> "7284","Skene gland carcinoma","umls","C1335352"
> "7284","Skene gland carcinoma","umls","C1527427"
> "7284","Skene gland carcinoma","mondo","0004173"
> "1586","rheumatic fever","icd10cm","I00"
> "1586","rheumatic fever","icd10cm","I00-I02"
> "1586","rheumatic fever","icd9cm","390"
> "1586","rheumatic fever","icd9cm","390-392.99"
> "1586","rheumatic fever","mesh","D012213"
> "1586","rheumatic fever","umls","C0035436"
> "1586","rheumatic fever","umls","C0264743"
> "1586","rheumatic fever","mondo","0017767"
> "1587","thrombocytopenia due to platelet alloimmunization","umls","C0272286"
> "1587","thrombocytopenia due to platelet alloimmunization","mondo","0002048"
> "1584","acute chest syndrome","icd9cm","517.3"
> "1584","acute chest syndrome","mesh","D056586"
> "1584","acute chest syndrome","umls","C0742343"
> "1584","acute chest syndrome","mondo","0005632"
> "5482","cystadenofibroma","mesh","D062625"
> "5482","cystadenofibroma","umls","C0334317"
> "5482","cystadenofibroma","mondo","0003464"
> "9455","lipid storage disease","icd10cm","E75.6"
> "9455","lipid storage disease","icd9cm","272.7"
> "9455","lipid storage disease","icd9cm","272.8"
> "9455","lipid storage disease","mesh","D008064"
> "9455","lipid storage disease","umls","C0023794"
> "9455","lipid storage disease","umls","C0029591"
> "9455","lipid storage disease","mondo","0019245"
> "5480","ovarian endometrioid adenofibroma","mondo","0003463"
> "7289","secretory uterine corpus endometrioid adenocarcinoma","umls","C1336907"
> "7289","secretory uterine corpus endometrioid adenocarcinoma","mondo","0004174"
> "0060428","chromosome 2q32-q33 deletion syndrome","icd10cm","Q93.5"
> "0060428","chromosome 2q32-q33 deletion syndrome","mondo","0012864"
> "0060423","chromosome 6q11-q14 deletion syndrome","mondo","0013299"
> "0060422","chromosome 6pter-p24 deletion syndrome","icd10cm","Q93.5"
> "0060422","chromosome 6pter-p24 deletion syndrome","mondo","0012948"
> "0060421","chromosome 5q12 deletion syndrome","mondo","0014298"
> "0060420","chromosome 4q21 deletion syndrome","mondo","0013292"
> "0060427","chromosome Xp21 deletion syndrome","icd10cm","Q99.8"
> "0060427","chromosome Xp21 deletion syndrome","mondo","0010399"
> "0060426","chromosome 19p13.13 deletion syndrome","mondo","0013336"
> "0060425","chromosome 8q21.11 deletion syndrome","icd10cm","Q93.5"
> "0060425","chromosome 8q21.11 deletion syndrome","mondo","0013646"
> "0060424","chromosome 6q24-q25 deletion syndrome","mondo","0013025"
> "9452","fatty liver disease","icd10cm","K70.0"
> "9452","fatty liver disease","icd9cm","571.0"
> "9452","fatty liver disease","mesh","D005234"
> "9452","fatty liver disease","mesh","D005235"
> "9452","fatty liver disease","umls","C0015695"
> "9452","fatty liver disease","umls","C0015696"
> "9452","fatty liver disease","mondo","0004790"
> "5658","lipid-rich carcinoma","umls","C0334318"
> "5658","lipid-rich carcinoma","mondo","0003570"
> "5656","cranial nerve disease","icd10cm","G52.9"
> "5656","cranial nerve disease","icd9cm","352.9"
> "5656","cranial nerve disease","mesh","D003389"
> "5656","cranial nerve disease","umls","C0010266"
> "5656","cranial nerve disease","mondo","0003569"
> "5655","chiasmal syndrome","icd10cm","H47.4"
> "5655","chiasmal syndrome","icd9cm","377.5"
> "5655","chiasmal syndrome","umls","C0155307"
> "5655","chiasmal syndrome","mondo","0003568"
> "0111395","mucopolysaccharidosis type IIIA","umls","C0086647"
> "13341","parasitic conjunctivitis","icd9cm","372.15"
> "13341","parasitic conjunctivitis","umls","C0155148"
> "13341","parasitic conjunctivitis","mondo","0001690"
> "6419","tetralogy of Fallot","icd10cm","Q21.3"
> "6419","tetralogy of Fallot","icd9cm","745.2"
> "6419","tetralogy of Fallot","mesh","D013771"
> "6419","tetralogy of Fallot","umls","C0039685"
> "6419","tetralogy of Fallot","mondo","0008542"
> "12465","secondary hyperparathyroidism of renal origin","icd10cm","N25.81"
> "12465","secondary hyperparathyroidism of renal origin","icd9cm","588.81"
> "12465","secondary hyperparathyroidism of renal origin","umls","C0271847"
> "12465","secondary hyperparathyroidism of renal origin","mondo","0001530"
> "12466","secondary hyperparathyroidism","mesh","D006962"
> "12466","secondary hyperparathyroidism","umls","C0020503"
> "12466","secondary hyperparathyroidism","mondo","0006964"
> "13949","interstitial cystitis","mesh","D018856"
> "13949","interstitial cystitis","umls","C0282488"
> "13949","interstitial cystitis","mondo","0018301"
> "3917","pancreatic serous cystadenoma","umls","C1335316"
> "3917","pancreatic serous cystadenoma","mondo","0002808"
> "3911","progeria","icd10cm","E34.8"
> "3911","progeria","mesh","D011371"
> "3911","progeria","umls","C0033300"
> "3911","progeria","mondo","0008310"
> "3910","lung adenocarcinoma","mesh","C538231"
> "3910","lung adenocarcinoma","umls","C0152013"
> "3910","lung adenocarcinoma","umls","C1335060"
> "3910","lung adenocarcinoma","mondo","0005061"
> "3919","pancreatic serous cystic neoplasm","umls","C1518875"
> "3919","pancreatic serous cystic neoplasm","mondo","0002810"
> "3918","pancreatic cystadenoma","umls","C0341486"
> "3918","pancreatic cystadenoma","mondo","0002809"
> "6733","intrahepatic bile duct cystadenoma","umls","C1334257"
> "6733","intrahepatic bile duct cystadenoma","mondo","0003979"
> "8310","sclerosing adenosis of breast","umls","C1335931"
> "8310","sclerosing adenosis of breast","mondo","0004531"
> "6735","schwannoma of jugular foramen","umls","C1334300"
> "6735","schwannoma of jugular foramen","mondo","0003980"
> "0090128","Carvajal syndrome","mondo","0011581"
> "9923","developmental coordination disorder","icd10cm","F82"
> "9923","developmental coordination disorder","icd9cm","315.4"
> "9923","developmental coordination disorder","mesh","D019957"
> "9923","developmental coordination disorder","umls","C0011757"
> "9923","developmental coordination disorder","mondo","0004922"
> "216","dental caries","icd10cm","K02"
> "216","dental caries","icd10cm","K02.6"
> "216","dental caries","icd10cm","K02.9"
> "216","dental caries","icd9cm","521.0"
> "216","dental caries","icd9cm","521.00"
> "216","dental caries","icd9cm","521.07"
> "216","dental caries","mesh","D003731"
> "216","dental caries","umls","C0011334"
> "216","dental caries","umls","C1456145"
> "216","dental caries","mondo","0005276"
> "217","enamel caries","icd9cm","521.01"
> "217","enamel caries","umls","C0266853"
> "217","enamel caries","mondo","0002233"
> "214","teeth hard tissue disease","icd10cm","K03.8"
> "214","teeth hard tissue disease","icd10cm","K03.89"
> "214","teeth hard tissue disease","icd9cm","521.8"
> "214","teeth hard tissue disease","icd9cm","521.89"
> "214","teeth hard tissue disease","umls","C0029770"
> "214","teeth hard tissue disease","mondo","0002220"
> "0060849","osteoporosis-pseudoglioma syndrome","mesh","C536063"
> "0060849","osteoporosis-pseudoglioma syndrome","umls","C0432252"
> "0060849","osteoporosis-pseudoglioma syndrome","mondo","0009820"
> "0060848","early infantile epileptic encephalopathy 9","mondo","0010246"
> "210","heel spur","icd10cm","M77.3"
> "210","heel spur","icd10cm","M77.30"
> "210","heel spur","icd9cm","726.73"
> "210","heel spur","mesh","D036982"
> "210","heel spur","umls","C0158322"
> "210","heel spur","mondo","0002209"
> "0060844","Norrie disease","mesh","C537849"
> "0060844","Norrie disease","umls","C0266526"
> "0060844","Norrie disease","mondo","0010691"
> "0060847","Leri-Weill dyschondrosteosis","mesh","C537119"
> "0060847","Leri-Weill dyschondrosteosis","umls","C0265309"
> "0060847","Leri-Weill dyschondrosteosis","mondo","0007481"
> "10883","herpangina","icd10cm","B08.5"
> "10883","herpangina","icd9cm","074.0"
> "10883","herpangina","mesh","D006557"
> "10883","herpangina","umls","C0019338"
> "10883","herpangina","mondo","0005791"
> "0060841","isolated microphthalmia 8","icd10cm","Q11.0"
> "0060841","isolated microphthalmia 8","mondo","0014050"
> "0060840","isolated microphthalmia 1","icd10cm","Q11.0"
> "0060840","isolated microphthalmia 1","mondo","0009631"
> "0060843","hereditary neuropathy with liability to pressure palsies","mesh","C536965"
> "0060843","hereditary neuropathy with liability to pressure palsies","umls","C0393814"
> "0060843","hereditary neuropathy with liability to pressure palsies","mondo","0008087"
> "0060842","isolated microphthalmia 3","icd10cm","Q11.0"
> "0060842","isolated microphthalmia 3","mondo","0012604"
> "6088","acute stress disorder","icd9cm","308.3"
> "6088","acute stress disorder","umls","C0029488"
> "6088","acute stress disorder","mondo","0003763"
> "6089","pediatric leptomeningeal melanoma","umls","C1332976"
> "6089","pediatric leptomeningeal melanoma","mondo","0003764"
> "6086","malignant leptomeningeal tumor","umls","C1334596"
> "6086","malignant leptomeningeal tumor","mondo","0003762"
> "6084","pediatric ovarian germ cell tumor","umls","C0796664"
> "6084","pediatric ovarian germ cell tumor","mondo","0003760"
> "6085","meningeal melanoma","umls","C1334386"
> "6085","meningeal melanoma","mondo","0003761"
> "6082","pediatric testicular germ cell tumor","umls","C0796663"
> "6082","pediatric testicular germ cell tumor","mondo","0003758"
> "6083","childhood ovarian endodermal sinus tumor","umls","C1332993"
> "6083","childhood ovarian endodermal sinus tumor","mondo","0003759"
> "12070","Dieulafoy lesion","icd10cm","K31.82"
> "12070","Dieulafoy lesion","icd9cm","537.84"
> "12070","Dieulafoy lesion","umls","C1135229"
> "12070","Dieulafoy lesion","mondo","0001427"
> "11574","streptococcal meningitis","icd10cm","G00.2"
> "11574","streptococcal meningitis","icd9cm","320.2"
> "11574","streptococcal meningitis","umls","C0154639"
> "11574","streptococcal meningitis","mondo","0001316"
> "11573","listeriosis","icd10cm","A32"
> "11573","listeriosis","icd10cm","A32.9"
> "11573","listeriosis","icd9cm","027.0"
> "11573","listeriosis","mesh","D008088"
> "11573","listeriosis","umls","C0023860"
> "11573","listeriosis","mondo","0005828"
> "11572","Listeria meningitis","mesh","D008584"
> "11572","Listeria meningitis","umls","C0025293"
> "11572","Listeria meningitis","mondo","0006836"
> "0111538","paramyotonia congenita of Von Eulenburg","umls","C0221055"
> "0070077","schizophrenia 1","mondo","0008414"
> "0050473","Alstrom syndrome","mesh","D056769"
> "0050473","Alstrom syndrome","umls","C0268425"
> "0050473","Alstrom syndrome","mondo","0008763"
> "0050472","monilethrix","icd10cm","Q84.1"
> "0050472","monilethrix","mesh","D056734"
> "0050472","monilethrix","umls","C0546966"
> "0050472","monilethrix","mondo","0008009"
> "0050471","Carney complex","mesh","D056733"
> "0050471","Carney complex","umls","C0406810"
> "0050471","Carney complex","umls","C1854540"
> "0050471","Carney complex","umls","C2607929"
> "0050471","Carney complex","mondo","0015285"
> "0050470","Donohue syndrome","mesh","D056731"
> "0050470","Donohue syndrome","umls","C0265344"
> "0050470","Donohue syndrome","umls","C0271695"
> "0050470","Donohue syndrome","mondo","0009517"
> "0050477","Liddle syndrome","mesh","D056929"
> "0050477","Liddle syndrome","umls","C0221043"
> "0050477","Liddle syndrome","mondo","0008323"
> "0050476","Barth syndrome","icd10cm","E78.71"
> "0050476","Barth syndrome","mesh","D056889"
> "0050476","Barth syndrome","umls","C0574083"
> "0050476","Barth syndrome","mondo","0010543"
> "0050475","Weill-Marchesani syndrome","mesh","D056846"
> "0050475","Weill-Marchesani syndrome","umls","C0265313"
> "0050475","Weill-Marchesani syndrome","umls","C1869114"
> "0050475","Weill-Marchesani syndrome","umls","C1869115"
> "0050475","Weill-Marchesani syndrome","mondo","0018096"
> "0050474","Netherton syndrome","mesh","D056770"
> "0050474","Netherton syndrome","umls","C0265962"
> "0050474","Netherton syndrome","mondo","0009735"
> "3649","pyruvate decarboxylase deficiency","icd10cm","E74.4"
> "3649","pyruvate decarboxylase deficiency","mesh","D015325"
> "3649","pyruvate decarboxylase deficiency","umls","C0034345"
> "3649","pyruvate decarboxylase deficiency","mondo","0019169"
> "3646","necrosis of pituitary","umls","C0271558"
> "3646","necrosis of pituitary","mondo","0002721"
> "3644","hypothalamic neoplasm","mesh","D007029"
> "3644","hypothalamic neoplasm","umls","C0020659"
> "3644","hypothalamic neoplasm","mondo","0006799"
> "3643","sella turcica neoplasm","umls","C0748616"
> "3643","sella turcica neoplasm","mondo","0002720"
> "3642","empty sella syndrome","mesh","D004652"
> "3642","empty sella syndrome","umls","C0014008"
> "3642","empty sella syndrome","mondo","0006740"
> "3641","conus medullaris neoplasm","umls","C1333153"
> "3641","conus medullaris neoplasm","mondo","0002719"
> "3640","central nervous system teratoma","umls","C1332895"
> "3640","central nervous system teratoma","mondo","0002718"
> "0111103","maturity-onset diabetes of the young type 4","mondo","0011667"
> "0111102","maturity-onset diabetes of the young type 3","mondo","0010894"
> "0111101","maturity-onset diabetes of the young type 5","mondo","0007669"
> "0111100","maturity-onset diabetes of the young type 2","mondo","0007453"
> "0111107","maturity-onset diabetes of the young type 9","mondo","0012818"
> "0111106","maturity-onset diabetes of the young type 7","mondo","0012513"
> "0111105","maturity-onset diabetes of the young type 8","mondo","0012348"
> "0111104","maturity-onset diabetes of the young type 6","mondo","0011668"
> "2559","opiate dependence","icd10cm","F11.2"
> "2559","opiate dependence","icd9cm","304.0"
> "2559","opiate dependence","icd9cm","304.00"
> "2559","opiate dependence","mesh","D009293"
> "2559","opiate dependence","umls","C0524662"
> "2559","opiate dependence","mondo","0005530"
> "0111109","maturity-onset diabetes of the young type 11","mondo","0013242"
> "0111108","maturity-onset diabetes of the young type 10","mondo","0013240"
> "11476","osteoporosis","icd10cm","M81.0"
> "11476","osteoporosis","icd9cm","733.0"
> "11476","osteoporosis","icd9cm","733.00"
> "11476","osteoporosis","mesh","D010024"
> "11476","osteoporosis","umls","C0029456"
> "11476","osteoporosis","mondo","0005298"
> "11472","subglottis cancer","icd10cm","C32.2"
> "11472","subglottis cancer","icd9cm","161.2"
> "11472","subglottis cancer","umls","C0153485"
> "11472","subglottis cancer","mondo","0001293"
> "0060196","amyotrophic lateral sclerosis type 4","icd10cm","G12.2"
> "0060196","amyotrophic lateral sclerosis type 4","mondo","0011223"
> "5015","fibrolamellar carcinoma","mesh","C537258"
> "5015","fibrolamellar carcinoma","umls","C0334287"
> "5015","fibrolamellar carcinoma","mondo","0006210"
> "0050699","Dent disease","mesh","C538212"
> "0050699","Dent disease","mesh","C564487"
> "0050699","Dent disease","mesh","D057973"
> "0050699","Dent disease","umls","C0878681"
> "0050699","Dent disease","umls","C1845167"
> "0050699","Dent disease","umls","C1848336"
> "0050699","Dent disease","mondo","0015612"
> "0050697","chorioamnionitis","mesh","D002821"
> "0050697","chorioamnionitis","mondo","0000409"
> "0050694","Brown-Vialetto-Van Laere syndrome","mesh","C537111"
> "0050694","Brown-Vialetto-Van Laere syndrome","mondo","0000406"
> "0050693","Brooke-Spiegler syndrome","mondo","0011512"
> "0050692","Brody myopathy","mesh","C536607"
> "0050692","Brody myopathy","mondo","0010977"
> "0050691","branchiooculofacial syndrome","mondo","0007235"
> "0050690","brachyolmia","mondo","0015262"
> "4419","benign deep fibrous histiocytoma","umls","C1266125"
> "4419","benign deep fibrous histiocytoma","mondo","0002990"
> "4418","cutaneous fibrous histiocytoma","mesh","D018219"
> "4418","cutaneous fibrous histiocytoma","umls","C0002991"
> "4418","cutaneous fibrous histiocytoma","umls","C0346049"
> "4418","cutaneous fibrous histiocytoma","mondo","0006717"
> "13306","diphtheritic cystitis","icd10cm","A36.85"
> "13306","diphtheritic cystitis","icd9cm","032.84"
> "13306","diphtheritic cystitis","umls","C0152954"
> "13306","diphtheritic cystitis","mondo","0001681"
> "4415","fibrous histiocytoma","mesh","D018219"
> "4415","fibrous histiocytoma","umls","C0206644"
> "4415","fibrous histiocytoma","mondo","0002989"
> "4413","cervix melanoma","umls","C0877611"
> "4413","cervix melanoma","mondo","0002988"
> "4411","hepatitis E","mesh","D016751"
> "4411","hepatitis E","umls","C0085293"
> "4411","hepatitis E","mondo","0005788"
> "918","liver inflammatory pseudotumor","umls","C1333967"
> "918","liver inflammatory pseudotumor","mondo","0004726"
> "914","peliosis hepatis","icd10cm","K76.4"
> "914","peliosis hepatis","mesh","D010382"
> "914","peliosis hepatis","umls","C0030781"
> "914","peliosis hepatis","mondo","0004717"
> "917","liver leiomyoma","umls","C1333968"
> "917","liver leiomyoma","mondo","0004723"
> "916","liver benign neoplasm","umls","C1333419"
> "916","liver benign neoplasm","umls","C1333976"
> "916","liver benign neoplasm","mondo","0004721"
> "910","occipital lobe neoplasm","icd10cm","C71.4"
> "910","occipital lobe neoplasm","icd9cm","191.4"
> "910","occipital lobe neoplasm","umls","C0153638"
> "910","occipital lobe neoplasm","umls","C1263889"
> "910","occipital lobe neoplasm","mondo","0004709"
> "913","atrophic muscular disease","mesh","D020966"
> "913","atrophic muscular disease","umls","C0752352"
> "913","atrophic muscular disease","mondo","0004714"
> "9541","osteosclerotic myeloma","umls","C1510415"
> "9541","osteosclerotic myeloma","mondo","0004815"
> "0070137","autosomal recessive cutis laxa type IIB","icd10cm","Q82.8"
> "0070137","autosomal recessive cutis laxa type IIB","mondo","0013051"
> "11814","urinary bladder anterior wall cancer","icd10cm","C67.3"
> "11814","urinary bladder anterior wall cancer","icd9cm","188.3"
> "11814","urinary bladder anterior wall cancer","umls","C0153611"
> "11814","urinary bladder anterior wall cancer","mondo","0001376"
> "11816","vitreous syneresis","icd10cm","H43.81"
> "11816","vitreous syneresis","icd9cm","379.21"
> "11816","vitreous syneresis","umls","C0155366"
> "11816","vitreous syneresis","mondo","0001377"
> "11817","urachus cancer","icd10cm","C67.7"
> "11817","urachus cancer","icd9cm","188.7"
> "11817","urachus cancer","umls","C0153615"
> "11817","urachus cancer","mondo","0001378"
> "11811","urinary bladder posterior wall cancer","icd10cm","C67.4"
> "11811","urinary bladder posterior wall cancer","icd9cm","188.4"
> "11811","urinary bladder posterior wall cancer","umls","C0153612"
> "11811","urinary bladder posterior wall cancer","mondo","0001373"
> "0110418","retinitis pigmentosa Y-linked","icd10cm","H35.5"
> "0110418","retinitis pigmentosa Y-linked","mondo","0010761"
> "0110419","retinitis pigmentosa with or without situs inversus","icd10cm","H35.5"
> "0110419","retinitis pigmentosa with or without situs inversus","mondo","0014186"
> "0110416","retinitis pigmentosa 24","icd10cm","H35.5"
> "0110416","retinitis pigmentosa 24","mondo","0010259"
> "0110417","retinitis pigmentosa 34","icd10cm","H35.5"
> "0110417","retinitis pigmentosa 34","mondo","0010374"
> "0110414","retinitis pigmentosa 3","icd10cm","H35.5"
> "0110414","retinitis pigmentosa 3","mondo","0010227"
> "0110415","retinitis pigmentosa 2","icd10cm","H35.5"
> "0110415","retinitis pigmentosa 2","mondo","0010723"
> "0110412","retinitis pigmentosa 23","icd10cm","H35.5"
> "0110412","retinitis pigmentosa 23","mondo","0010320"
> "11819","ureter cancer","icd10cm","C66"
> "11819","ureter cancer","icd9cm","189.2"
> "11819","ureter cancer","mesh","D014516"
> "11819","ureter cancer","umls","C0153619"
> "11819","ureter cancer","mondo","0008627"
> "0110410","retinitis pigmentosa 69","icd10cm","H35.5"
> "0110410","retinitis pigmentosa 69","mondo","0014345"
> "0110411","retinitis pigmentosa 60","icd10cm","H35.5"
> "0110411","retinitis pigmentosa 60","mondo","0013516"
> "0110674","congenital myasthenic syndrome 17","mondo","0014578"
> "0110675","congenital myasthenic syndrome 11","mondo","0014588"
> "0060210","amyotrophic lateral sclerosis type 19","mondo","0014223"
> "0060211","amyotrophic lateral sclerosis type 20","mondo","0014181"
> "0060212","amyotrophic lateral sclerosis type 21","mondo","0011632"
> "7169","lung occult large cell carcinoma","umls","C1335095"
> "7169","lung occult large cell carcinoma","mondo","0004128"
> "0060214","FTDALS2","mondo","0014395"
> "0060215","Balo concentric sclerosis","icd10cm","G31.81"
> "0060215","Balo concentric sclerosis","icd10cm","G37.0"
> "0060215","Balo concentric sclerosis","icd9cm","341.1"
> "0060215","Balo concentric sclerosis","mesh","D002549"
> "0060215","Balo concentric sclerosis","umls","C0004712"
> "0060215","Balo concentric sclerosis","umls","C0007795"
> "0060215","Balo concentric sclerosis","umls","C0205710"
> "0060215","Balo concentric sclerosis","mondo","0016430"
> "0060216","Cogan syndrome","icd10cm","H16.32"
> "0060216","Cogan syndrome","mesh","D055952"
> "0060216","Cogan syndrome","umls","C0271270"
> "0060216","Cogan syndrome","mondo","0015453"
> "0060217","Cogan-Reese syndrome","umls","C1168173"
> "0060217","Cogan-Reese syndrome","mondo","0020370"
> "0060218","CREST syndrome","icd10cm","M34.1"
> "0060218","CREST syndrome","mesh","D017675"
> "0060218","CREST syndrome","umls","C0206138"
> "0060218","CREST syndrome","umls","C1527226"
> "0060218","CREST syndrome","mondo","0019563"
> "7160","rectum leiomyoma","umls","C1335682"
> "7160","rectum leiomyoma","mondo","0004125"
> "7166","thyroiditis","icd10cm","E06"
> "7166","thyroiditis","icd10cm","E06.9"
> "7166","thyroiditis","icd9cm","245"
> "7166","thyroiditis","icd9cm","245.9"
> "7166","thyroiditis","mesh","D013966"
> "7166","thyroiditis","umls","C0040147"
> "7166","thyroiditis","mondo","0004126"
> "7165","subacute thyroiditis","icd10cm","E06.1"
> "7165","subacute thyroiditis","icd9cm","245.1"
> "7165","subacute thyroiditis","mesh","D013968"
> "7165","subacute thyroiditis","umls","C0040149"
> "7165","subacute thyroiditis","mondo","0006982"
> "8078","childhood central nervous system germinoma","umls","C1332953"
> "8078","childhood central nervous system germinoma","mondo","0004452"
> "12899","benign lymphoepithelial lesion of salivary gland","icd10cm","K11.8"
> "12899","benign lymphoepithelial lesion of salivary gland","umls","C0266995"
> "12899","benign lymphoepithelial lesion of salivary gland","mondo","0001598"
> "12895","keratoconjunctivitis sicca","mesh","D007638"
> "12895","keratoconjunctivitis sicca","umls","C0022575"
> "12895","keratoconjunctivitis sicca","mondo","0006818"
> "12894","Sjogren's syndrome","icd10cm","M35.0"
> "12894","Sjogren's syndrome","icd10cm","M35.00"
> "12894","Sjogren's syndrome","icd9cm","710.2"
> "12894","Sjogren's syndrome","mesh","D012859"
> "12894","Sjogren's syndrome","umls","C0086981"
> "12894","Sjogren's syndrome","umls","C1527336"
> "12894","Sjogren's syndrome","mondo","0010030"
> "12897","submandibular gland disease","mesh","D013364"
> "12897","submandibular gland disease","umls","C0038557"
> "12897","submandibular gland disease","mondo","0001597"
> "8072","sarcomatous intrahepatic cholangiocarcinoma","umls","C1519184"
> "8072","sarcomatous intrahepatic cholangiocarcinoma","mondo","0004451"
> "0110678","congenital myasthenic syndrome 4A","mondo","0011600"
> "10686","lactocele","icd10cm","N64.89"
> "10686","lactocele","icd9cm","611.5"
> "10686","lactocele","mesh","C535998"
> "10686","lactocele","umls","C0152243"
> "10686","lactocele","mondo","0001099"
> "0110679","congenital myasthenic syndrome 4C","mondo","0012157"
> "1217","fascioloidiasis","mesh","D005213"
> "1217","fascioloidiasis","umls","C0015655"
> "1217","fascioloidiasis","mondo","0005759"
> "12165","retinal lattice degeneration","icd10cm","H35.41"
> "12165","retinal lattice degeneration","icd9cm","362.63"
> "12165","retinal lattice degeneration","umls","C0154856"
> "12165","retinal lattice degeneration","mondo","0001455"
> "1214","tympanosclerosis","icd9cm","385.09"
> "1214","tympanosclerosis","umls","C0155477"
> "1214","tympanosclerosis","mondo","0001443"
> "12164","Blessig's cysts","icd10cm","H35.42"
> "12164","Blessig's cysts","icd9cm","362.62"
> "12164","Blessig's cysts","umls","C0154855"
> "12164","Blessig's cysts","mondo","0001454"
> "0111273","NARP syndrome","umls","C1328349"
> "0050998","nonprogressive cerebellar ataxia with mental retardation","mondo","0013886"
> "0050999","autosomal recessive spinocerebellar ataxia 10","mondo","0013392"
> "12166","cobblestone retinal degeneration","icd10cm","H35.43"
> "12166","cobblestone retinal degeneration","icd9cm","362.61"
> "12166","cobblestone retinal degeneration","umls","C0154854"
> "12166","cobblestone retinal degeneration","mondo","0001456"
> "1115","sarcoma","icd10cm","C49"
> "1115","sarcoma","icd9cm","171"
> "1115","sarcoma","icd9cm","171.9"
> "1115","sarcoma","umls","C0153519"
> "1115","sarcoma","mondo","0005089"
> "1114","esophagus sarcoma","umls","C1333466"
> "1114","esophagus sarcoma","mondo","0001204"
> "1441","autosomal dominant cerebellar ataxia","mesh","D020754"
> "1441","autosomal dominant cerebellar ataxia","umls","C0087012"
> "1441","autosomal dominant cerebellar ataxia","mondo","0020380"
> "1116","pertussis","kegg","05133"
> "1116","pertussis","mesh","D001885"
> "1116","pertussis","umls","C0006015"
> "1116","pertussis","mondo","0005077"
> "0050990","episodic ataxia type 2","mondo","0007163"
> "0050991","episodic ataxia type 3","mondo","0011682"
> "0050992","episodic ataxia type 4","mondo","0011681"
> "0050993","episodic ataxia type 5","mondo","0013464"
> "0050994","episodic ataxia type 6","mondo","0012982"
> "0050995","episodic ataxia type 7","mondo","0012755"
> "0050996","episodic ataxia type 8","mondo","0014476"
> "2007","degeneration of macula and posterior pole","icd10cm","H35.3"
> "2007","degeneration of macula and posterior pole","icd9cm","362.5"
> "2007","degeneration of macula and posterior pole","umls","C0339436"
> "2007","degeneration of macula and posterior pole","mondo","0002175"
> "12163","senile reticular retinal degeneration","icd9cm","362.64"
> "12163","senile reticular retinal degeneration","umls","C0154857"
> "12163","senile reticular retinal degeneration","mondo","0001453"
> "12162","pseudoretinitis pigmentosa","icd10cm","H35.45"
> "12162","pseudoretinitis pigmentosa","icd9cm","362.65"
> "12162","pseudoretinitis pigmentosa","umls","C0154858"
> "12162","pseudoretinitis pigmentosa","mondo","0001452"
> "4584","choroid plexus meningioma","umls","C0431118"
> "4584","choroid plexus meningioma","mondo","0003053"
> "4587","benign meningioma","mesh","D008579"
> "4587","benign meningioma","umls","C0281784"
> "4587","benign meningioma","mondo","0003054"
> "12168","ulnar nerve lesion","icd10cm","G56.2"
> "12168","ulnar nerve lesion","icd10cm","G56.20"
> "12168","ulnar nerve lesion","icd9cm","354.2"
> "12168","ulnar nerve lesion","umls","C1288279"
> "12168","ulnar nerve lesion","mondo","0001458"
> "6789","vulvar childhood botryoid-type embryonal rhabdomyosarcoma","umls","C1332946"
> "6789","vulvar childhood botryoid-type embryonal rhabdomyosarcoma","mondo","0003995"
> "6788","vagina botryoid rhabdomyosarcoma","umls","C1511275"
> "6788","vagina botryoid rhabdomyosarcoma","mondo","0003994"
> "13865","facial neuralgia","mesh","D005156"
> "13865","facial neuralgia","umls","C0015467"
> "13865","facial neuralgia","mondo","0001818"
> "6524","malignant ciliary body melanoma","umls","C0346379"
> "6524","malignant ciliary body melanoma","mondo","0003912"
> "248","trachea leiomyoma","mesh","D014134"
> "248","trachea leiomyoma","umls","C0040582"
> "248","trachea leiomyoma","umls","C1336772"
> "248","trachea leiomyoma","mondo","0002318"
> "13864","trochlear nerve disease","icd10cm","H49.1"
> "13864","trochlear nerve disease","icd9cm","378.53"
> "13864","trochlear nerve disease","mesh","D020432"
> "13864","trochlear nerve disease","umls","C0271375"
> "13864","trochlear nerve disease","umls","C0423092"
> "13864","trochlear nerve disease","umls","C0751939"
> "13864","trochlear nerve disease","mondo","0007002"
> "4788","intracranial primitive neuroectodermal tumor","umls","C1334246"
> "4788","intracranial primitive neuroectodermal tumor","mondo","0003142"
> "4787","cerebellopontine angle primitive neuroectodermal","umls","C1332904"
> "4787","cerebellopontine angle primitive neuroectodermal","mondo","0003141"
> "4784","immune-complex glomerulonephritis","umls","C0744421"
> "4784","immune-complex glomerulonephritis","mondo","0003140"
> "4783","mesangial proliferative glomerulonephritis","umls","C0221238"
> "4783","mesangial proliferative glomerulonephritis","mondo","0003139"
> "4782","subacute glomerulonephritis","umls","C1263744"
> "4782","subacute glomerulonephritis","mondo","0003138"
> "4781","diffuse glomerulonephritis","umls","C0859036"
> "4781","diffuse glomerulonephritis","mondo","0003137"
> "4780","anti-basement membrane glomerulonephritis","umls","C1332309"
> "4780","anti-basement membrane glomerulonephritis","mondo","0003136"
> "5821","methotrexate-associated lymphoproliferation","umls","C1334749"
> "5821","methotrexate-associated lymphoproliferation","mondo","0003657"
> "5820","composite lymphoma","mesh","D058617"
> "5820","composite lymphoma","umls","C0545080"
> "5820","composite lymphoma","mondo","0005710"
> "5823","pediatric lymphoma","umls","C1332979"
> "5823","pediatric lymphoma","mondo","0003659"
> "5822","gray zone lymphoma","umls","C1333878"
> "5822","gray zone lymphoma","mondo","0003658"
> "5825","adult lymphoma","umls","C1332206"
> "5825","adult lymphoma","mondo","0003660"
> "14172","rheumatic congestive heart failure","icd10cm","I09.81"
> "14172","rheumatic congestive heart failure","icd9cm","398.91"
> "14172","rheumatic congestive heart failure","umls","C0155582"
> "14172","rheumatic congestive heart failure","mondo","0001899"
> "5826","breast lymphoma","umls","C0349669"
> "5826","breast lymphoma","mondo","0003661"
> "5829","uterine ligament endometrioid adenocarcinoma","umls","C1519868"
> "5829","uterine ligament endometrioid adenocarcinoma","mondo","0003663"
> "5828","endometrioid ovary carcinoma","umls","C0346163"
> "5828","endometrioid ovary carcinoma","mondo","0006335"
> "11260","rabies","icd10cm","A82"
> "11260","rabies","icd10cm","A82.9"
> "11260","rabies","icd9cm","071"
> "11260","rabies","mesh","D011818"
> "11260","rabies","umls","C0034494"
> "11260","rabies","mondo","0019173"
> "11267","keratomalacia","icd10cm","H18.44"
> "11267","keratomalacia","icd9cm","371.45"
> "11267","keratomalacia","mesh","C536156"
> "11267","keratomalacia","umls","C0152455"
> "11267","keratomalacia","mondo","0001250"
> "11266","Hantavirus hemorrhagic fever with renal syndrome","icd10cm","A98.5"
> "11266","Hantavirus hemorrhagic fever with renal syndrome","icd9cm","078.6"
> "11266","Hantavirus hemorrhagic fever with renal syndrome","mesh","D006480"
> "11266","Hantavirus hemorrhagic fever with renal syndrome","umls","C0019101"
> "11266","Hantavirus hemorrhagic fever with renal syndrome","mondo","0005784"
> "11265","trachoma","icd10cm","A71"
> "11265","trachoma","icd10cm","A71.0"
> "11265","trachoma","icd10cm","A71.1"
> "11265","trachoma","icd10cm","A71.9"
> "11265","trachoma","icd9cm","076"
> "11265","trachoma","icd9cm","076.0"
> "11265","trachoma","icd9cm","076.1"
> "11265","trachoma","icd9cm","076.9"
> "11265","trachoma","mesh","D014141"
> "11265","trachoma","umls","C0040592"
> "11265","trachoma","umls","C0153107"
> "11265","trachoma","umls","C0153108"
> "11265","trachoma","mondo","0001249"
> "14179","X-linked agammaglobulinemia","mesh","C537409"
> "14179","X-linked agammaglobulinemia","umls","C0221026"
> "14179","X-linked agammaglobulinemia","mondo","0010421"
> "13862","acute closed-angle glaucoma","icd10cm","H40.21"
> "13862","acute closed-angle glaucoma","icd9cm","365.22"
> "13862","acute closed-angle glaucoma","umls","C0154946"
> "13862","acute closed-angle glaucoma","mondo","0001817"
> "13781","hypermobility syndrome","icd10cm","M35.7"
> "13781","hypermobility syndrome","icd9cm","728.5"
> "13781","hypermobility syndrome","umls","C0152093"
> "13781","hypermobility syndrome","mondo","0001798"
> "0070324","systemic Epstein-Barr virus-positive T-cell lymphoma of childhood","icd10cm","D47.9"
> "0070324","systemic Epstein-Barr virus-positive T-cell lymphoma of childhood","mesh","D008232"
> "11988","conjunctival concretion","icd10cm","H11.12"
> "11988","conjunctival concretion","icd9cm","372.54"
> "11988","conjunctival concretion","umls","C0155162"
> "11988","conjunctival concretion","mondo","0001412"
> "10457","Legionnaires' disease","icd10cm","A48.1"
> "10457","Legionnaires' disease","icd9cm","482.84"
> "10457","Legionnaires' disease","mesh","D007877"
> "10457","Legionnaires' disease","umls","C0023241"
> "10457","Legionnaires' disease","mondo","0005824"
> "193","reproductive organ cancer","umls","C0178830"
> "193","reproductive organ cancer","mondo","0002149"
> "192","sex cord-gonadal stromal tumor","mesh","D018312"
> "192","sex cord-gonadal stromal tumor","umls","C0206724"
> "192","sex cord-gonadal stromal tumor","mondo","0006055"
> "11983","Prader-Willi syndrome","icd10cm","Q87.1"
> "11983","Prader-Willi syndrome","icd9cm","759.81"
> "11983","Prader-Willi syndrome","mesh","D011218"
> "11983","Prader-Willi syndrome","umls","C0032897"
> "11983","Prader-Willi syndrome","mondo","0008300"
> "3749","urethral verrucous carcinoma","umls","C1519827"
> "3749","urethral verrucous carcinoma","mondo","0002763"
> "9155","mucocutaneous leishmaniasis","icd10cm","B55.2"
> "9155","mucocutaneous leishmaniasis","icd9cm","085.5"
> "9155","mucocutaneous leishmaniasis","mesh","D007897"
> "9155","mucocutaneous leishmaniasis","umls","C1328252"
> "9155","mucocutaneous leishmaniasis","mondo","0005859"
> "0070117","Meckel syndrome 3","icd10cm","Q61.9"
> "0070117","Meckel syndrome 3","mondo","0011821"
> "0070114","Niemann-Pick disease type C2","icd10cm","E75.2"
> "0070114","Niemann-Pick disease type C2","mondo","0011873"
> "0070115","Meckel syndrome 1","icd10cm","Q61.9"
> "0070115","Meckel syndrome 1","mondo","0009571"
> "0070112","Niemann-Pick disease type B","icd10cm","E75.2"
> "0070112","Niemann-Pick disease type B","mondo","0011871"
> "0070113","Niemann-Pick disease type C1","icd10cm","E75.2"
> "0070113","Niemann-Pick disease type C1","mondo","0009757"
> "9153","variola minor","icd9cm","050.1"
> "9153","variola minor","mesh","D012899"
> "9153","variola minor","umls","C0001906"
> "9153","variola minor","mondo","0004720"
> "0070111","Niemann-Pick disease type A","icd10cm","E75.2"
> "0070111","Niemann-Pick disease type A","mondo","0009756"
> "2763","ethmoid sinus squamous cell carcinoma","umls","C1333477"
> "2763","ethmoid sinus squamous cell carcinoma","mondo","0002416"
> "2762","bone carcinoma","umls","C0700110"
> "2762","bone carcinoma","mondo","0002415"
> "421","hair disease","mesh","D006201"
> "421","hair disease","umls","C0018500"
> "421","hair disease","mondo","0002917"
> "9159","gas gangrene","icd10cm","A48.0"
> "9159","gas gangrene","icd9cm","040.0"
> "9159","gas gangrene","mesh","D005738"
> "9159","gas gangrene","umls","C0017105"
> "9159","gas gangrene","mondo","0005767"
> "2766","ethmoid sinus adenocarcinoma","umls","C1333472"
> "2766","ethmoid sinus adenocarcinoma","mondo","0002418"
> "0070118","Meckel syndrome 4","icd10cm","Q61.9"
> "0070118","Meckel syndrome 4","mondo","0012626"
> "0070119","Meckel syndrome 5","icd10cm","Q61.9"
> "0070119","Meckel syndrome 5","mondo","0012695"
> "9483","ulcerative blepharitis","icd10cm","H01.01"
> "9483","ulcerative blepharitis","icd9cm","373.01"
> "9483","ulcerative blepharitis","umls","C0155173"
> "9483","ulcerative blepharitis","mondo","0004799"
> "7903","intracranial chondrosarcoma","umls","C1334238"
> "7903","intracranial chondrosarcoma","mondo","0004392"
> "9487","Meckel's diverticulum","icd10cm","Q43.0"
> "9487","Meckel's diverticulum","icd9cm","751.0"
> "9487","Meckel's diverticulum","mesh","D008467"
> "9487","Meckel's diverticulum","umls","C0025037"
> "9487","Meckel's diverticulum","mondo","0007955"
> "7907","mixed astrocytoma-ependymoma","umls","C0280791"
> "7907","mixed astrocytoma-ependymoma","mondo","0004393"
> "6271","gastric cardia adenocarcinoma","umls","C1333762"
> "6271","gastric cardia adenocarcinoma","mondo","0003835"
> "6270","gastric cardia carcinoma","umls","C1333763"
> "6270","gastric cardia carcinoma","mondo","0003834"
> "6275","TSH producing pituitary tumor","umls","C0346303"
> "6275","TSH producing pituitary tumor","mondo","0003837"
> "6274","malignant thyroid stimulating hormone producing neoplasm of pituitary gland","umls","C1334627"
> "6274","malignant thyroid stimulating hormone producing neoplasm of pituitary gland","mondo","0003836"
> "12246","histoplasmosis meningitis","icd9cm","115.91"
> "12246","histoplasmosis meningitis","umls","C0153277"
> "12246","histoplasmosis meningitis","mondo","0001471"
> "6276","malignant ACTH producing neoplasm of pituitary gland","umls","C1334556"
> "6276","malignant ACTH producing neoplasm of pituitary gland","mondo","0006069"
> "6278","ovarian mucinous malignant adenofibroma","mondo","0003839"
> "0110809","hereditary spastic paraplegia 57","icd10cm","G11.4"
> "0110809","hereditary spastic paraplegia 57","mondo","0014295"
> "240","iris disease","mesh","D007499"
> "240","iris disease","umls","C0022078"
> "240","iris disease","mondo","0002289"
> "0060737","junctional epidermolysis bullosa Herlitz type","icd10cm","Q81.1"
> "0060737","junctional epidermolysis bullosa Herlitz type","mondo","0009182"
> "9733","renal tuberculosis","icd9cm","016.0"
> "9733","renal tuberculosis","icd9cm","016.00"
> "9733","renal tuberculosis","mesh","D014398"
> "9733","renal tuberculosis","umls","C0041328"
> "9733","renal tuberculosis","mondo","0005938"
> "9735","acute allergic mucoid otitis media","icd9cm","381.05"
> "9735","acute allergic mucoid otitis media","umls","C0155419"
> "9735","acute allergic mucoid otitis media","mondo","0004864"
> "9736","blue drum syndrome","icd9cm","381.02"
> "9736","blue drum syndrome","umls","C0395863"
> "9736","blue drum syndrome","mondo","0004865"
> "9739","eustachian tube disease","icd9cm","381.8"
> "9739","eustachian tube disease","icd9cm","381.89"
> "9739","eustachian tube disease","umls","C0155435"
> "9739","eustachian tube disease","mondo","0004866"
> "0110805","hereditary spastic paraplegia 53","icd10cm","G11.4"
> "0110805","hereditary spastic paraplegia 53","mondo","0013962"
> "0110804","hereditary spastic paraplegia 52","mondo","0013552"
> "4084","testicular trophoblastic tumor","umls","C1515301"
> "4084","testicular trophoblastic tumor","mondo","0002871"
> "0110807","hereditary spastic paraplegia 55","icd10cm","G11.4"
> "0110807","hereditary spastic paraplegia 55","mondo","0014020"
> "4085","trophoblastic neoplasm","mesh","D014328"
> "4085","trophoblastic neoplasm","umls","C0041182"
> "4085","trophoblastic neoplasm","mondo","0002872"
> "854","collagen disease","mesh","D003095"
> "854","collagen disease","umls","C0009326"
> "854","collagen disease","mondo","0021103"
> "856","biotinidase deficiency","icd10cm","D81.810"
> "856","biotinidase deficiency","mesh","D028921"
> "856","biotinidase deficiency","umls","C0220754"
> "856","biotinidase deficiency","mondo","0009665"
> "857","multiple carboxylase deficiency","icd10cm","D81.81"
> "857","multiple carboxylase deficiency","icd10cm","D81.819"
> "857","multiple carboxylase deficiency","mesh","D009100"
> "857","multiple carboxylase deficiency","umls","C0026755"
> "857","multiple carboxylase deficiency","mondo","0015454"
> "850","lung disease","icd10cm","J98.4"
> "850","lung disease","mesh","D008171"
> "850","lung disease","umls","C0024115"
> "850","lung disease","mondo","0005275"
> "851","Bartholin's duct cyst","icd10cm","N75.0"
> "851","Bartholin's duct cyst","icd9cm","616.2"
> "851","Bartholin's duct cyst","umls","C0004767"
> "851","Bartholin's duct cyst","mondo","0004593"
> "3454","brain infarction","mesh","D020520"
> "3454","brain infarction","umls","C0751955"
> "3454","brain infarction","mondo","0005394"
> "853","polymyalgia rheumatica","icd10cm","M35.3"
> "853","polymyalgia rheumatica","icd9cm","725"
> "853","polymyalgia rheumatica","mesh","D011111"
> "853","polymyalgia rheumatica","umls","C0032533"
> "853","polymyalgia rheumatica","mondo","0019735"
> "0110801","hereditary spastic paraplegia 49","icd10cm","G11.4"
> "0110801","hereditary spastic paraplegia 49","mondo","0014016"
> "3458","breast adenocarcinoma","umls","C0858252"
> "3458","breast adenocarcinoma","mondo","0004988"
> "3459","breast carcinoma","mesh","D001943"
> "3459","breast carcinoma","umls","C0678222"
> "3459","breast carcinoma","mondo","0004989"
> "859","holocarboxylase synthetase deficiency","icd10cm","D81.818"
> "859","holocarboxylase synthetase deficiency","mesh","D028922"
> "859","holocarboxylase synthetase deficiency","umls","C0268581"
> "859","holocarboxylase synthetase deficiency","mondo","0009666"
> "0110800","hereditary spastic paraplegia 48","icd10cm","G11.4"
> "0110800","hereditary spastic paraplegia 48","mondo","0013342"
> "13169","spermatic cord cancer","icd10cm","C63.1"
> "13169","spermatic cord cancer","icd9cm","187.6"
> "13169","spermatic cord cancer","umls","C0153603"
> "13169","spermatic cord cancer","mondo","0001654"
> "0110803","hereditary spastic paraplegia 51","mondo","0013401"
> "0110802","hereditary spastic paraplegia 50","mondo","0013048"
> "0110067","juvenile amyotrophic lateral sclerosis with dementia","mondo","0008781"
> "0110066","amelogenesis imperfecta type 1G","icd10cm","K00.5"
> "0110066","amelogenesis imperfecta type 1G","mondo","0008771"
> "0110065","amelogenesis imperfecta type 1F","icd10cm","K00.5"
> "0110065","amelogenesis imperfecta type 1F","mondo","0014560"
> "0110064","amelogenesis imperfecta type 1H","icd10cm","K00.5"
> "0110064","amelogenesis imperfecta type 1H","mondo","0014540"
> "0110063","amelogenesis imperfecta hypomaturation type 2A5","icd10cm","K00.5"
> "0110063","amelogenesis imperfecta hypomaturation type 2A5","mondo","0014385"
> "0110062","amelogenesis imperfecta hypomaturation type 2A4","icd10cm","K00.5"
> "0110062","amelogenesis imperfecta hypomaturation type 2A4","mondo","0013906"
> "0110061","amelogenesis imperfecta hypomaturation type 2A3","icd10cm","K00.5"
> "0110061","amelogenesis imperfecta hypomaturation type 2A3","mondo","0013181"
> "0110060","amelogenesis imperfecta hypomaturation type 2A2","icd10cm","K00.5"
> "0110060","amelogenesis imperfecta hypomaturation type 2A2","mondo","0012926"
> "0110069","FTDALS4","mondo","0014641"
> "0110068","FTDALS3","mondo","0014640"
> "14145","malignant anus melanoma","umls","C0349538"
> "14145","malignant anus melanoma","mondo","0006081"
> "14146","ureterolithiasis","icd9cm","592.1"
> "14146","ureterolithiasis","mesh","D053039"
> "14146","ureterolithiasis","umls","C0041952"
> "14146","ureterolithiasis","mondo","0007009"
> "13160","scrotum melanoma","umls","C1331544"
> "13160","scrotum melanoma","mondo","0001652"
> "5223","infertility","mesh","D007246"
> "5223","infertility","umls","C0021359"
> "5223","infertility","mondo","0005047"
> "0040060","ketoprofen photoallergic dermatitis","umls","C0570547"
> "5221","chronic polyneuropathy","umls","C1167650"
> "5221","chronic polyneuropathy","mondo","0003335"
> "11750","Bordetella parapertussis whooping cough","icd10cm","A37.1"
> "11750","Bordetella parapertussis whooping cough","icd9cm","033.1"
> "11750","Bordetella parapertussis whooping cough","umls","C0275742"
> "11750","Bordetella parapertussis whooping cough","mondo","0001353"
> "0040065","quinidine allergy","umls","C0571881"
> "0040067","neomycin sulfate allergic contact dermatitis","umls","C1443961"
> "5224","acute hemorrhagic encephalitis","umls","C1332149"
> "5224","acute hemorrhagic encephalitis","mondo","0003337"
> "13113","cicatricial entropion","icd9cm","374.04"
> "13113","cicatricial entropion","umls","C0155191"
> "13113","cicatricial entropion","mondo","0001637"
> "13112","mechanical entropion","icd9cm","374.02"
> "13112","mechanical entropion","umls","C0155189"
> "13112","mechanical entropion","mondo","0001636"
> "13110","bladder squamous papilloma","umls","C1511199"
> "13110","bladder squamous papilloma","mondo","0001635"
> "13117","paronychia","icd10cm","L03.0"
> "13117","paronychia","mesh","D010304"
> "13117","paronychia","umls","C0030578"
> "13117","paronychia","mondo","0005898"
> "14499","Fabry disease","icd10cm","E75.21"
> "14499","Fabry disease","mesh","D000795"
> "14499","Fabry disease","umls","C0002986"
> "14499","Fabry disease","mondo","0010526"
> "14353","acute thyroiditis","icd10cm","E06.0"
> "14353","acute thyroiditis","icd9cm","245.0"
> "14353","acute thyroiditis","umls","C0001360"
> "14353","acute thyroiditis","mondo","0001949"
> "3069","astrocytoma","mesh","D001254"
> "3069","astrocytoma","umls","C0004114"
> "3069","astrocytoma","umls","C0750935"
> "3069","astrocytoma","mondo","0021636"
> "3068","glioblastoma multiforme","mesh","D005909"
> "3068","glioblastoma multiforme","umls","C0017636"
> "3068","glioblastoma multiforme","umls","C0278878"
> "3068","glioblastoma multiforme","umls","C1514422"
> "3068","glioblastoma multiforme","mondo","0018177"
> "14365","systemic primary carnitine deficiency disease","icd10cm","E71.41"
> "14365","systemic primary carnitine deficiency disease","icd9cm","277.81"
> "14365","systemic primary carnitine deficiency disease","mesh","C536778"
> "14365","systemic primary carnitine deficiency disease","umls","C0342788"
> "14365","systemic primary carnitine deficiency disease","mondo","0008919"
> "14495","dumping syndrome","icd10cm","K91.1"
> "14495","dumping syndrome","mesh","D004377"
> "14495","dumping syndrome","umls","C0013288"
> "14495","dumping syndrome","mondo","0001979"
> "4267","akinetic mutism","mesh","D000405"
> "4267","akinetic mutism","umls","C0001889"
> "4267","akinetic mutism","mondo","0005640"
> "1307","dementia","icd9cm","290.8"
> "1307","dementia","mesh","D003704"
> "1307","dementia","umls","C0154319"
> "1307","dementia","mondo","0001627"
> "12143","neurogenic bladder","icd9cm","596.54"
> "12143","neurogenic bladder","mesh","D001750"
> "12143","neurogenic bladder","umls","C0005697"
> "12143","neurogenic bladder","mondo","0001445"
> "0070289","primary autosomal recessive microcephaly 16","mondo","0014730"
> "495","sclerosing hemangioma","umls","C1509148"
> "495","sclerosing hemangioma","mondo","0006280"
> "496","spindle cell hemangioma","umls","C1304508"
> "496","spindle cell hemangioma","mondo","0016222"
> "492","acquired hemangioma","umls","C0856897"
> "492","acquired hemangioma","mondo","0003206"
> "12402","pyromania","icd10cm","F63.1"
> "12402","pyromania","icd9cm","312.33"
> "12402","pyromania","mesh","D005391"
> "12402","pyromania","umls","C0016142"
> "12402","pyromania","mondo","0001522"
> "12403","tinea pedis","icd10cm","B35.3"
> "12403","tinea pedis","icd9cm","110.4"
> "12403","tinea pedis","mesh","D014008"
> "12403","tinea pedis","umls","C0040259"
> "12403","tinea pedis","mondo","0005984"
> "12400","kleptomania","icd10cm","F63.2"
> "12400","kleptomania","icd9cm","312.32"
> "12400","kleptomania","mesh","D007174"
> "12400","kleptomania","umls","C0022734"
> "12400","kleptomania","mondo","0001520"
> "12401","intermittent explosive disorder","icd10cm","F60.3"
> "12401","intermittent explosive disorder","icd10cm","F63.81"
> "12401","intermittent explosive disorder","icd9cm","301.3"
> "12401","intermittent explosive disorder","icd9cm","312.34"
> "12401","intermittent explosive disorder","mesh","D007174"
> "12401","intermittent explosive disorder","umls","C0021776"
> "12401","intermittent explosive disorder","umls","C0152183"
> "12401","intermittent explosive disorder","mondo","0001521"
> "6477","invasive bladder transitional cell carcinoma","umls","C1334281"
> "6477","invasive bladder transitional cell carcinoma","mondo","0003890"
> "6476","clear cell variant infiltrating bladder urothelial carcinoma","umls","C1512737"
> "6476","clear cell variant infiltrating bladder urothelial carcinoma","mondo","0003889"
> "6474","childhood teratocarcinoma of the testis","umls","C1333008"
> "6474","childhood teratocarcinoma of the testis","mondo","0003888"
> "0060157","diffuse alopecia areata","mesh","C531609"
> "0060157","diffuse alopecia areata","umls","C0406458"
> "0060157","diffuse alopecia areata","umls","C1274706"
> "0060157","diffuse alopecia areata","umls","C1862862"
> "0060157","diffuse alopecia areata","umls","C2936778"
> "0060157","diffuse alopecia areata","umls","C3179487"
> "0060157","diffuse alopecia areata","umls","C3179488"
> "0060157","diffuse alopecia areata","umls","C3179489"
> "0060157","diffuse alopecia areata","mondo","0000687"
> "0060404","chromosome 17q12 deletion syndrome","icd10cm","Q93.5"
> "0060404","chromosome 17q12 deletion syndrome","mondo","0013797"
> "0060155","visual agnosia","mesh","C531604"
> "0060155","visual agnosia","umls","C2930796"
> "0060155","visual agnosia","mondo","0000685"
> "0060406","chromosome 18p deletion syndrome","mesh","C538309"
> "0060406","chromosome 18p deletion syndrome","umls","C0432442"
> "0060406","chromosome 18p deletion syndrome","mondo","0007800"
> "0060401","chromosome 16q22 deletion syndrome","mondo","0013798"
> "0060400","chromosome 16p12.2-p11.2 deletion syndrome","icd10cm","Q93.5"
> "0060400","chromosome 16p12.2-p11.2 deletion syndrome","mondo","0013320"
> "0060403","chromosome 17q11.2 deletion syndrome, 1.4Mb","icd10cm","Q85.0"
> "0060403","chromosome 17q11.2 deletion syndrome, 1.4Mb","mondo","0013357"
> "0060402","chromosome 17p13.1 deletion syndrome","mesh","D054221"
> "0060402","chromosome 17p13.1 deletion syndrome","mondo","0013415"
> "7757","childhood leukemia","umls","C1332977"
> "7757","childhood leukemia","mondo","0004355"
> "7756","neonatal leukemia","umls","C0235813"
> "7756","neonatal leukemia","mondo","0004354"
> "0060409","chromosome 1p32-p31 deletion syndrome","icd10cm","Q93.5"
> "0060409","chromosome 1p32-p31 deletion syndrome","mondo","0013396"
> "7750","adult brain ependymoma","umls","C1332186"
> "7750","adult brain ependymoma","mondo","0004352"
> "0060159","organic acidemia","mondo","0000688"
> "7752","extrahepatic biliary papillomatosis","umls","C1333511"
> "7752","extrahepatic biliary papillomatosis","mondo","0004353"
> "0070281","primary autosomal recessive microcephaly 19","mondo","0054716"
> "3939","lipomatous cancer","umls","C0346117"
> "3939","lipomatous cancer","mondo","0002813"
> "0070286","primary autosomal recessive microcephaly 3","mondo","0011488"
> "3930","otitis interna","umls","C1168225"
> "3930","otitis interna","mondo","0002008"
> "3933","anterior compartment syndrome","icd10cm","M76.81"
> "3933","anterior compartment syndrome","mesh","D000868"
> "3933","anterior compartment syndrome","umls","C0003152"
> "3933","anterior compartment syndrome","mondo","0006648"
> "11603","infant gynecomastia","icd10cm","P83.4"
> "11603","infant gynecomastia","icd9cm","778.7"
> "11603","infant gynecomastia","mesh","D006177"
> "11603","infant gynecomastia","umls","C1449721"
> "11603","infant gynecomastia","mondo","0001323"
> "8331","perineural angioma","umls","C1335382"
> "8331","perineural angioma","mondo","0004533"
> "8336","childhood choriocarcinoma of the ovary","umls","C1332987"
> "8336","childhood choriocarcinoma of the ovary","mondo","0004535"
> "9531","latent syphilis","icd10cm","A53.0"
> "9531","latent syphilis","icd9cm","097.1"
> "9531","latent syphilis","mesh","D013592"
> "9531","latent syphilis","umls","C0039133"
> "9531","latent syphilis","mondo","0005822"
> "8335","microglandular adenosis of breast","umls","C1334753"
> "8335","microglandular adenosis of breast","mondo","0004534"
> "5195","peripheral nervous system ganglioneuroblastoma","umls","C1335387"
> "5195","peripheral nervous system ganglioneuroblastoma","mondo","0003327"
> "8338","villoglandular variant cervical mucinous adenocarcinoma","umls","C4289808"
> "8338","villoglandular variant cervical mucinous adenocarcinoma","mondo","0006141"
> "8339","intestinal variant cervical mucinous adenocarcinoma","umls","C1516422"
> "8339","intestinal variant cervical mucinous adenocarcinoma","mondo","0004537"
> "6712","anterior spinal artery syndrome","mesh","D020759"
> "6712","anterior spinal artery syndrome","umls","C0221069"
> "6712","anterior spinal artery syndrome","mondo","0006650"
> "6713","cerebrovascular disease","icd10cm","I60-I69"
> "6713","cerebrovascular disease","icd10cm","I63.9"
> "6713","cerebrovascular disease","icd10cm","I67.9"
> "6713","cerebrovascular disease","icd9cm","430-438.99"
> "6713","cerebrovascular disease","icd9cm","437.9"
> "6713","cerebrovascular disease","mesh","D002561"
> "6713","cerebrovascular disease","mesh","D020521"
> "6713","cerebrovascular disease","umls","C0007820"
> "6713","cerebrovascular disease","umls","C0038454"
> "6713","cerebrovascular disease","mondo","0011057"
> "9905","follicular mucinosis","icd10cm","L65.2"
> "9905","follicular mucinosis","mesh","D000507"
> "9905","follicular mucinosis","umls","C0002173"
> "9905","follicular mucinosis","mondo","0006551"
> "9903","meibomian cyst","icd10cm","H00.1"
> "9903","meibomian cyst","icd9cm","373.2"
> "9903","meibomian cyst","mesh","D017043"
> "9903","meibomian cyst","umls","C0007933"
> "9903","meibomian cyst","mondo","0005844"
> "9908","internal hordeolum","icd10cm","H00.02"
> "9908","internal hordeolum","icd9cm","373.12"
> "9908","internal hordeolum","umls","C0085690"
> "9908","internal hordeolum","mondo","0004917"
> "9909","hordeolum","icd10cm","H00.01"
> "9909","hordeolum","mesh","D006726"
> "9909","hordeolum","umls","C0019917"
> "9909","hordeolum","mondo","0005800"
> "13963","nuclear senile cataract","icd9cm","366.16"
> "13963","nuclear senile cataract","umls","C0271166"
> "13963","nuclear senile cataract","mondo","0001847"
> "176","cardiovascular cancer","umls","C0497243"
> "176","cardiovascular cancer","mondo","0002100"
> "4044","skeletal muscle neoplasm","umls","C1335971"
> "4044","skeletal muscle neoplasm","mondo","0002848"
> "4045","muscle cancer","icd10cm","C49"
> "4045","muscle cancer","mesh","D009217"
> "4045","muscle cancer","mesh","D019042"
> "4045","muscle cancer","umls","C0027095"
> "4045","muscle cancer","umls","C0684743"
> "4045","muscle cancer","mondo","0005864"
> "13757","excessive tearing","icd10cm","H04.2"
> "13757","excessive tearing","icd10cm","H04.20"
> "13757","excessive tearing","icd9cm","375.2"
> "13757","excessive tearing","icd9cm","375.20"
> "13757","excessive tearing","mesh","D007766"
> "13757","excessive tearing","umls","C0152227"
> "13757","excessive tearing","mondo","0001793"
> "4047","liver rhabdomyosarcoma","umls","C1333975"
> "4047","liver rhabdomyosarcoma","mondo","0002849"
> "4043","skeletal muscle cancer","umls","C1334619"
> "4043","skeletal muscle cancer","mondo","0002847"
> "4048","central nervous system rhabdomyosarcoma","umls","C1332891"
> "4048","central nervous system rhabdomyosarcoma","mondo","0002850"
> "4049","mediastinum rhabdomyosarcoma","umls","C1334677"
> "4049","mediastinum rhabdomyosarcoma","mondo","0002851"
> "172","clear cell acanthoma","mesh","D049309"
> "172","clear cell acanthoma","umls","C0333992"
> "172","clear cell acanthoma","mondo","0002086"
> "3665","diffuse cutaneous mastocytosis","icd10cm","D47.01"
> "3665","diffuse cutaneous mastocytosis","mesh","D034701"
> "3665","diffuse cutaneous mastocytosis","umls","C0024901"
> "3665","diffuse cutaneous mastocytosis","mondo","0019315"
> "3664","mast cell neoplasm","icd10cm","D47.09"
> "3664","mast cell neoplasm","umls","C0334664"
> "3664","mast cell neoplasm","mondo","0002724"
> "0050459","hyperphosphatemia","mesh","D054559"
> "0050459","hyperphosphatemia","umls","C0085681"
> "0050459","hyperphosphatemia","mondo","0000328"
> "0050458","juvenile myelomonocytic leukemia","icd10cm","C93.3"
> "0050458","juvenile myelomonocytic leukemia","icd10cm","C93.30"
> "0050458","juvenile myelomonocytic leukemia","mesh","D054429"
> "0050458","juvenile myelomonocytic leukemia","umls","C0349639"
> "0050458","juvenile myelomonocytic leukemia","mondo","0011908"
> "3663","cutaneous mastocytosis","icd10cm","D47.01"
> "3663","cutaneous mastocytosis","mesh","D034701"
> "3663","cutaneous mastocytosis","umls","C1136033"
> "3663","cutaneous mastocytosis","mondo","0019023"
> "0050328","congenital hypothyroidism","icd10cm","E00.1"
> "0050328","congenital hypothyroidism","icd10cm","E03.1"
> "0050328","congenital hypothyroidism","icd9cm","243"
> "0050328","congenital hypothyroidism","mesh","D003409"
> "0050328","congenital hypothyroidism","umls","C0010308"
> "0050328","congenital hypothyroidism","umls","C0342200"
> "0050328","congenital hypothyroidism","mondo","0018612"
> "0050454","periventricular nodular heterotopia","mesh","D054091"
> "0050454","periventricular nodular heterotopia","umls","C1848213"
> "0050454","periventricular nodular heterotopia","umls","C1868720"
> "0050454","periventricular nodular heterotopia","mondo","0020341"
> "0050457","Sertoli cell-only syndrome","mesh","D054331"
> "0050457","Sertoli cell-only syndrome","umls","C1384583"
> "0050457","Sertoli cell-only syndrome","mondo","0010595"
> "0050456","Buruli ulcer disease","icd10cm","A31.1"
> "0050456","Buruli ulcer disease","mesh","D054312"
> "0050456","Buruli ulcer disease","umls","C0085568"
> "0050456","Buruli ulcer disease","mondo","0000327"
> "3669","intermittent claudication","icd10cm","I73.9"
> "3669","intermittent claudication","mesh","D007383"
> "3669","intermittent claudication","umls","C0021775"
> "3669","intermittent claudication","mondo","0005295"
> "0050450","Gitelman syndrome","mesh","D053579"
> "0050450","Gitelman syndrome","umls","C0268450"
> "0050450","Gitelman syndrome","mondo","0009904"
> "0050453","lissencephaly","icd10cm","Q04.3"
> "0050453","lissencephaly","icd10cm","Q04.8"
> "0050453","lissencephaly","mesh","D054082"
> "0050453","lissencephaly","umls","C0266463"
> "0050453","lissencephaly","umls","C0266483"
> "0050453","lissencephaly","mondo","0018838"
> "0050452","mevalonic aciduria","icd10cm","M04.1"
> "0050452","mevalonic aciduria","mesh","D054078"
> "0050452","mevalonic aciduria","umls","C0342731"
> "0050452","mevalonic aciduria","umls","C0398691"
> "0050452","mevalonic aciduria","umls","C1959626"
> "0050452","mevalonic aciduria","mondo","0012481"
> "0080029","autosomal recessive spinocerebellar ataxia 16","mondo","0014339"
> "0080028","spondyloepimetaphyseal dysplasia, Strudwick type","mondo","0008476"
> "0080021","Schmid metaphyseal chondrodysplasia","mondo","0007983"
> "0080020","Jansen's metaphyseal chondrodysplasia","mondo","0007982"
> "0080026","otospondylomegaepiphyseal dysplasia","mondo","0008975"
> "0111129","focal segmental glomerulosclerosis 2","icd10cm","N04.1"
> "0111129","focal segmental glomerulosclerosis 2","mondo","0011390"
> "0111128","focal segmental glomerulosclerosis 1","icd10cm","N04.1"
> "0111128","focal segmental glomerulosclerosis 1","mondo","0011303"
> "0111125","nephronophthisis 18","mondo","0014374"
> "0111124","nephronophthisis 16","mondo","0014158"
> "0111127","nephronophthisis 20","mondo","0014997"
> "0111126","nephronophthisis 19","mondo","0014537"
> "0111121","nephronophthisis 13","mondo","0013718"
> "0111120","nephronophthisis 9","mondo","0013444"
> "0111123","nephronophthisis 15","mondo","0013917"
> "0111122","nephronophthisis 14","mondo","0013916"
> "11459","pseudotumor cerebri","icd10cm","G93.2"
> "11459","pseudotumor cerebri","icd9cm","348.2"
> "11459","pseudotumor cerebri","mesh","D011559"
> "11459","pseudotumor cerebri","umls","C0033845"
> "11459","pseudotumor cerebri","mondo","0009468"
> "11457","brain compression","icd10cm","G93.5"
> "11457","brain compression","icd9cm","348.4"
> "11457","brain compression","umls","C0009592"
> "11457","brain compression","mondo","0001291"
> "11452","perinatal jaundice due to hepatocellular damage","icd9cm","774.4"
> "11452","perinatal jaundice due to hepatocellular damage","umls","C0158976"
> "11452","perinatal jaundice due to hepatocellular damage","mondo","0006595"
> "3593","epithelioid trophoblastic tumor","umls","C1266159"
> "3593","epithelioid trophoblastic tumor","mondo","0016787"
> "3590","gestational trophoblastic neoplasm","icd10cm","O01"
> "3590","gestational trophoblastic neoplasm","icd10cm","O01.0"
> "3590","gestational trophoblastic neoplasm","icd10cm","O01.9"
> "3590","gestational trophoblastic neoplasm","icd9cm","630"
> "3590","gestational trophoblastic neoplasm","mesh","D006828"
> "3590","gestational trophoblastic neoplasm","mesh","D031901"
> "3590","gestational trophoblastic neoplasm","umls","C0020217"
> "3590","gestational trophoblastic neoplasm","umls","C0278796"
> "3590","gestational trophoblastic neoplasm","umls","C1135868"
> "3590","gestational trophoblastic neoplasm","mondo","0018944"
> "3596","placental site trophoblastic tumor","mesh","D018245"
> "3596","placental site trophoblastic tumor","umls","C0206666"
> "3596","placental site trophoblastic tumor","mondo","0020552"
> "5039","myoblastoma","mesh","D009379"
> "5039","myoblastoma","umls","C0027043"
> "5039","myoblastoma","mondo","0003250"
> "5032","pineal gland cancer","icd10cm","C75.3"
> "5032","pineal gland cancer","icd9cm","194.4"
> "5032","pineal gland cancer","mesh","D010871"
> "5032","pineal gland cancer","umls","C0031941"
> "5032","pineal gland cancer","umls","C0153655"
> "5032","pineal gland cancer","umls","C1412004"
> "5032","pineal gland cancer","mondo","0003249"
> "5030","pineal parenchymal tumor of intermediate differentiation","umls","C1367859"
> "5030","pineal parenchymal tumor of intermediate differentiation","mondo","0006369"
> "5031","adult pineal parenchymal tumor","umls","C0280794"
> "5031","adult pineal parenchymal tumor","mondo","0003248"
> "4435","cavernous sinus meningioma","umls","C1332865"
> "4435","cavernous sinus meningioma","mondo","0002996"
> "4434","small intestine neuroendocrine neoplasm","umls","C1336005"
> "4434","small intestine neuroendocrine neoplasm","mondo","0018510"
> "4437","skull base meningioma","umls","C1335976"
> "4437","skull base meningioma","mondo","0002998"
> "4436","anterior cranial fossa meningioma","umls","C1332301"
> "4436","anterior cranial fossa meningioma","mondo","0002997"
> "10120","eyelid degenerative disease","icd9cm","374.50"
> "10120","eyelid degenerative disease","umls","C0155209"
> "10120","eyelid degenerative disease","mondo","0000941"
> "4430","somatostatinoma","mesh","D013005"
> "4430","somatostatinoma","umls","C0037661"
> "4430","somatostatinoma","mondo","0006976"
> "4433","pancreatic delta cell neoplasm","umls","C1335301"
> "4433","pancreatic delta cell neoplasm","mondo","0002994"
> "4432","pancreatic somatostatinoma","umls","C1368041"
> "4432","pancreatic somatostatinoma","mondo","0002993"
> "4439","central nervous system germ cell tumor","umls","C1332880"
> "4439","central nervous system germ cell tumor","mondo","0003000"
> "4438","central nervous system germinoma","umls","C1333813"
> "4438","central nervous system germinoma","mondo","0002999"
> "0090107","autosomal dominant hypocalcemia 1","mondo","0011013"
> "0090106","Bh4-deficient hyperphenylalaninemia A","mesh","C535325"
> "0090106","Bh4-deficient hyperphenylalaninemia A","umls","C0878676"
> "0090106","Bh4-deficient hyperphenylalaninemia A","mondo","0009863"
> "0090105","autosomal recessive hypercholesterolemia","icd10cm","E78.0"
> "0090105","autosomal recessive hypercholesterolemia","mondo","0011374"
> "974","upper respiratory tract disease","icd9cm","478.1"
> "974","upper respiratory tract disease","icd9cm","478.19"
> "974","upper respiratory tract disease","umls","C0029581"
> "974","upper respiratory tract disease","mondo","0004867"
> "0090103","Huntington's disease-like 1","icd10cm","G10"
> "0090103","Huntington's disease-like 1","mondo","0011299"
> "0090102","autosomal dominant macrothrombocytopenia TUBB1-related","icd10cm","D69.4"
> "0090102","autosomal dominant macrothrombocytopenia TUBB1-related","mondo","0013141"
> "971","tendinitis","icd10cm","M77.9"
> "971","tendinitis","mesh","D052256"
> "971","tendinitis","umls","C0039503"
> "971","tendinitis","mondo","0004857"
> "970","tenosynovitis","mesh","D013717"
> "970","tenosynovitis","umls","C0039520"
> "970","tenosynovitis","mondo","0004855"
> "0111381","IVIC syndrome","umls","C1327918"
> "0111383","autosomal dominant keratitis","mesh","C537022"
> "0111383","autosomal dominant keratitis","umls","C1835698"
> "0111382","ischiocoxopodopatellar syndrome","mesh","C535540"
> "0111382","ischiocoxopodopatellar syndrome","mesh","C536307"
> "0111382","ischiocoxopodopatellar syndrome","umls","C1840061"
> "0111382","ischiocoxopodopatellar syndrome","umls","C1868581"
> "979","angioid streaks of choroid","icd9cm","363.43"
> "979","angioid streaks of choroid","umls","C0002983"
> "979","angioid streaks of choroid","mondo","0004882"
> "0090108","autosomal dominant hypocalcemia 2","mondo","0014146"
> "10127","cerebral artery occlusion","icd9cm","434"
> "10127","cerebral artery occlusion","icd9cm","434.9"
> "10127","cerebral artery occlusion","umls","C0028790"
> "10127","cerebral artery occlusion","mondo","0000944"
> "0110658","congenital myasthenic syndrome 15","mondo","0014542"
> "0110659","congenital myasthenic syndrome 7","mondo","0014468"
> "0110654","long QT syndrome 13","icd10cm","I45.8"
> "0110654","long QT syndrome 13","mondo","0013279"
> "0110655","long QT syndrome 14","icd10cm","I45.8"
> "0110655","long QT syndrome 14","mondo","0014548"
> "0110656","long QT syndrome 15","icd10cm","I45.8"
> "0110656","long QT syndrome 15","mondo","0014550"
> "0110657","congenital myasthenic syndrome 8","mondo","0014052"
> "0110650","long QT syndrome 9","icd10cm","I45.8"
> "0110650","long QT syndrome 9","mondo","0012736"
> "0110651","long QT syndrome 10","icd10cm","I45.8"
> "0110651","long QT syndrome 10","mondo","0012737"
> "0110652","long QT syndrome 11","icd10cm","I45.8"
> "0110652","long QT syndrome 11","mondo","0012738"
> "0110653","long QT syndrome 12","icd10cm","I45.8"
> "0110653","long QT syndrome 12","mondo","0013062"
> "3728","acute allergic sanguinous otitis media","icd9cm","381.06"
> "3728","acute allergic sanguinous otitis media","umls","C0155420"
> "3728","acute allergic sanguinous otitis media","mondo","0002757"
> "10471","patellar tendinitis","icd10cm","M76.5"
> "10471","patellar tendinitis","icd10cm","M76.50"
> "10471","patellar tendinitis","icd9cm","726.64"
> "10471","patellar tendinitis","umls","C0158317"
> "10471","patellar tendinitis","mondo","0001042"
> "0110386","retinitis pigmentosa 42","icd10cm","H35.5"
> "0110386","retinitis pigmentosa 42","mondo","0013052"
> "0110387","retinitis pigmentosa 9","icd10cm","H35.5"
> "0110387","retinitis pigmentosa 9","mondo","0008378"
> "0070309","absence epilepsy","mesh","D004832"
> "0070308","rippling muscle disease 1","mondo","0010868"
> "0110382","retinitis pigmentosa 48","icd10cm","H35.5"
> "0110382","retinitis pigmentosa 48","mondo","0013447"
> "0110383","retinitis pigmentosa 7","icd10cm","H35.5"
> "0110383","retinitis pigmentosa 7","mondo","0011974"
> "0110380","retinitis pigmentosa 62","icd10cm","H35.5"
> "0110380","retinitis pigmentosa 62","mondo","0013611"
> "0110381","retinitis pigmentosa 14","icd10cm","H35.5"
> "0110381","retinitis pigmentosa 14","mondo","0010827"
> "0070303","multiple epiphyseal dysplasia 1","mesh","C535501"
> "0070303","multiple epiphyseal dysplasia 1","umls","C1838280"
> "0070303","multiple epiphyseal dysplasia 1","mondo","0007561"
> "0070302","multiple epiphyseal dysplasia 7","mondo","0054680"
> "0070301","multiple epiphyseal dysplasia 6","mondo","0013591"
> "0070300","multiple epiphyseal dysplasia 4","mesh","C535504"
> "0070300","multiple epiphyseal dysplasia 4","umls","C1847593"
> "0070300","multiple epiphyseal dysplasia 4","mondo","0009189"
> "0070307","craniolenticulosutural dysplasia","mondo","0011911"
> "0070305","multiple epiphyseal dysplasia due to collagen 9 anomaly","mondo","0015627"
> "0070304","multiple epiphyseal dysplasia 3","mondo","0010964"
> "8927","learning disability","icd10cm","F81.9"
> "8927","learning disability","mesh","D007859"
> "8927","learning disability","umls","C0023186"
> "8927","learning disability","umls","C0751265"
> "8927","learning disability","mondo","0004681"
> "0110479","autosomal recessive nonsyndromic deafness 21","icd10cm","H90.3"
> "0110479","autosomal recessive nonsyndromic deafness 21","mondo","0011351"
> "8925","primary thrombocytopenia","icd10cm","D69.4"
> "8925","primary thrombocytopenia","icd10cm","D69.49"
> "8925","primary thrombocytopenia","icd9cm","287.39"
> "8925","primary thrombocytopenia","umls","C0477317"
> "8925","primary thrombocytopenia","mondo","0004680"
> "8924","autoimmune thrombocytopenic purpura","icd10cm","D69.3"
> "8924","autoimmune thrombocytopenic purpura","icd9cm","287.31"
> "8924","autoimmune thrombocytopenic purpura","mesh","D016553"
> "8924","autoimmune thrombocytopenic purpura","umls","C0398650"
> "8924","autoimmune thrombocytopenic purpura","mondo","0008558"
> "8923","skin melanoma","icd10cm","C43"
> "8923","skin melanoma","icd10cm","C43.9"
> "8923","skin melanoma","icd9cm","172"
> "8923","skin melanoma","icd9cm","172.9"
> "8923","skin melanoma","mesh","C562393"
> "8923","skin melanoma","umls","C0151779"
> "8923","skin melanoma","mondo","0005012"
> "11874","abnormal threshold of rods","icd10cm","H53.61"
> "11874","abnormal threshold of rods","icd9cm","368.63"
> "11874","abnormal threshold of rods","umls","C0155019"
> "11874","abnormal threshold of rods","mondo","0001396"
> "8920","leukoplakia of vagina","icd10cm","N89.4"
> "8920","leukoplakia of vagina","icd9cm","623.1"
> "8920","leukoplakia of vagina","umls","C0156385"
> "8920","leukoplakia of vagina","mondo","0004679"
> "0110470","autosomal recessive nonsyndromic deafness 15","icd10cm","H90.3"
> "0110470","autosomal recessive nonsyndromic deafness 15","mondo","0011160"
> "0110471","autosomal recessive nonsyndromic deafness 16","icd10cm","H90.3"
> "0110471","autosomal recessive nonsyndromic deafness 16","mondo","0011364"
> "0110472","autosomal recessive nonsyndromic deafness 17","icd10cm","H90.3"
> "0110472","autosomal recessive nonsyndromic deafness 17","mondo","0011279"
> "0110473","autosomal recessive nonsyndromic deafness 18A","icd10cm","H90.3"
> "0110473","autosomal recessive nonsyndromic deafness 18A","mondo","0011192"
> "0110474","autosomal recessive nonsyndromic deafness 18B","icd10cm","H90.3"
> "0110474","autosomal recessive nonsyndromic deafness 18B","mondo","0013985"
> "0110475","autosomal recessive nonsyndromic deafness 1A","icd10cm","H90.3"
> "0110475","autosomal recessive nonsyndromic deafness 1A","mondo","0009076"
> "8929","atrophic gastritis","icd10cm","K29.4"
> "8929","atrophic gastritis","icd9cm","535.1"
> "8929","atrophic gastritis","mesh","D005757"
> "8929","atrophic gastritis","umls","C0017154"
> "8929","atrophic gastritis","mondo","0006665"
> "0110477","autosomal recessive nonsyndromic deafness 2","icd10cm","H90.3"
> "0110477","autosomal recessive nonsyndromic deafness 2","mondo","0010807"
> "7103","diaphragma sellae meningioma","umls","C1333283"
> "7103","diaphragma sellae meningioma","mondo","0004108"
> "7105","epiglottis neoplasm","umls","C1290353"
> "7105","epiglottis neoplasm","mondo","0004109"
> "5410","pulmonary neuroendocrine tumor","umls","C1334452"
> "5410","pulmonary neuroendocrine tumor","mondo","0005454"
> "5411","lung oat cell carcinoma","umls","C0262584"
> "5411","lung oat cell carcinoma","mondo","0003436"
> "0060238","Van Maldergem syndrome","mesh","C536530"
> "0060238","Van Maldergem syndrome","umls","C1832390"
> "0060238","Van Maldergem syndrome","mondo","0017813"
> "0060239","Van der Woude syndrome","icd10cm","Q38.0"
> "0060239","Van der Woude syndrome","mesh","C536528"
> "0060239","Van der Woude syndrome","mesh","C563529"
> "0060239","Van der Woude syndrome","umls","C0175697"
> "0060239","Van der Woude syndrome","umls","C1834339"
> "0060239","Van der Woude syndrome","mondo","0019508"
> "0060232","branchiootic syndrome","icd10cm","Q87.0"
> "0060232","branchiootic syndrome","mondo","0018878"
> "0060233","cardiofaciocutaneous syndrome","icd10cm","Q87.8"
> "0060233","cardiofaciocutaneous syndrome","mondo","0015280"
> "0060230","basal ganglia calcification","mesh","C536275"
> "0060230","basal ganglia calcification","umls","C0393590"
> "0060230","basal ganglia calcification","mondo","0008947"
> "0060231","Bruck syndrome","icd10cm","M21.8"
> "0060231","Bruck syndrome","mondo","0017195"
> "0060236","xanthinuria","mesh","C562584"
> "0060236","xanthinuria","mesh","C566358"
> "0060236","xanthinuria","umls","C0268118"
> "0060236","xanthinuria","umls","C1863688"
> "0060236","xanthinuria","mondo","0018106"
> "0060237","Warburg micro syndrome","mesh","C536681"
> "0060237","Warburg micro syndrome","umls","C1838625"
> "0060237","Warburg micro syndrome","mondo","0016649"
> "0060234","Carpenter syndrome","mesh","C563187"
> "0060234","Carpenter syndrome","umls","C1275078"
> "0060234","Carpenter syndrome","mondo","0019012"
> "0060235","carnitine palmitoyltransferase II deficiency","mesh","C535589"
> "0060235","carnitine palmitoyltransferase II deficiency","umls","C0342790"
> "0060235","carnitine palmitoyltransferase II deficiency","mondo","0015515"
> "1681","heart septal defect","icd10cm","Q21"
> "1681","heart septal defect","icd10cm","Q21.9"
> "1681","heart septal defect","mesh","D006343"
> "1681","heart septal defect","umls","C0018816"
> "1681","heart septal defect","mondo","0002078"
> "1680","chronic cystitis","icd10cm","N30.2"
> "1680","chronic cystitis","icd9cm","595.2"
> "1680","chronic cystitis","umls","C0156268"
> "1680","chronic cystitis","mondo","0006030"
> "1682","congenital heart disease","icd10cm","Q24.9"
> "1682","congenital heart disease","icd9cm","746.9"
> "1682","congenital heart disease","mesh","D006330"
> "1682","congenital heart disease","umls","C0018798"
> "1682","congenital heart disease","mondo","0005453"
> "1687","neovascular glaucoma","mesh","D015355"
> "1687","neovascular glaucoma","umls","C0017609"
> "1687","neovascular glaucoma","mondo","0019783"
> "1686","glaucoma","icd10cm","H40"
> "1686","glaucoma","icd10cm","H40-H42"
> "1686","glaucoma","icd10cm","H40.9"
> "1686","glaucoma","icd9cm","365"
> "1686","glaucoma","icd9cm","365.9"
> "1686","glaucoma","mesh","D005901"
> "1686","glaucoma","umls","C0017601"
> "1686","glaucoma","mondo","0005041"
> "14756","autosomal dominant type IV Ehlers-Danlos syndrome","mondo","0007524"
> "0110311","hypertrophic cardiomyopathy 21","mondo","0013852"
> "12128","pica disease","icd9cm","307.52"
> "12128","pica disease","mesh","D010842"
> "12128","pica disease","umls","C0031873"
> "12128","pica disease","mondo","0001441"
> "0050628","advanced sleep phase syndrome","mondo","0015609"
> "0050951","hereditary ataxia","mondo","0000557"
> "14753","isovaleric acidemia","icd10cm","E71.110"
> "14753","isovaleric acidemia","mesh","C538167"
> "14753","isovaleric acidemia","umls","C0268575"
> "14753","isovaleric acidemia","mondo","0009475"
> "0060098","osteoblastoma","mesh","D018215"
> "0060098","osteoblastoma","mondo","0018936"
> "14777","benign familial neonatal epilepsy","mesh","D020936"
> "14777","benign familial neonatal epilepsy","umls","C0220669"
> "14777","benign familial neonatal epilepsy","mondo","0002016"
> "14775","brittle cornea syndrome","mesh","C536198"
> "14775","brittle cornea syndrome","umls","C0268342"
> "14775","brittle cornea syndrome","mondo","0009242"
> "14773","cartilage-hair hypoplasia","mesh","C535916"
> "14773","cartilage-hair hypoplasia","umls","C0220748"
> "14773","cartilage-hair hypoplasia","mondo","0009595"
> "14778","blepharophimosis, ptosis, and epicanthus inversus syndrome","mesh","C562419"
> "14778","blepharophimosis, ptosis, and epicanthus inversus syndrome","umls","C0220663"
> "14778","blepharophimosis, ptosis, and epicanthus inversus syndrome","mondo","0007201"
> "1468","labyrinthitis","icd10cm","H83.0"
> "1468","labyrinthitis","icd10cm","H83.09"
> "1468","labyrinthitis","icd9cm","386.3"
> "1468","labyrinthitis","icd9cm","386.30"
> "1468","labyrinthitis","mesh","D007762"
> "1468","labyrinthitis","umls","C0022893"
> "1468","labyrinthitis","mondo","0002008"
> "1467","serous labyrinthitis","icd9cm","386.31"
> "1467","serous labyrinthitis","umls","C0155504"
> "1467","serous labyrinthitis","mondo","0002006"
> "1461","cholesterol embolism","icd10cm","I75"
> "1461","cholesterol embolism","icd9cm","445"
> "1461","cholesterol embolism","mesh","D017700"
> "1461","cholesterol embolism","umls","C0149649"
> "1461","cholesterol embolism","mondo","0005568"
> "4239","alveolar soft part sarcoma","mesh","D018234"
> "4239","alveolar soft part sarcoma","umls","C0206657"
> "4239","alveolar soft part sarcoma","umls","C0279544"
> "4239","alveolar soft part sarcoma","umls","C0279985"
> "4239","alveolar soft part sarcoma","mondo","0011655"
> "13929","lacrimal duct obstruction","mesh","D007767"
> "13929","lacrimal duct obstruction","umls","C0022906"
> "13929","lacrimal duct obstruction","mondo","0001833"
> "4236","carcinosarcoma","mesh","D002296"
> "4236","carcinosarcoma","mesh","D018199"
> "4236","carcinosarcoma","mesh","D018200"
> "4236","carcinosarcoma","umls","C0007140"
> "4236","carcinosarcoma","umls","C0206627"
> "4236","carcinosarcoma","umls","C1334603"
> "4236","carcinosarcoma","mondo","0002928"
> "4235","spindle cell sarcoma","mesh","D012509"
> "4235","spindle cell sarcoma","umls","C0205945"
> "4235","spindle cell sarcoma","mondo","0002927"
> "4233","clear cell sarcoma","mesh","D018227"
> "4233","clear cell sarcoma","umls","C0206651"
> "4233","clear cell sarcoma","umls","C1332198"
> "4233","clear cell sarcoma","mondo","0002926"
> "4232","extraosseous Ewing sarcoma","umls","C1333514"
> "4232","extraosseous Ewing sarcoma","mondo","0018270"
> "4231","histiocytoma","mesh","D051642"
> "4231","histiocytoma","umls","C1509147"
> "4231","histiocytoma","mondo","0005509"
> "4230","smooth muscle cancer","umls","C1334620"
> "4230","smooth muscle cancer","mondo","0002924"
> "5591","eccrine papillary adenocarcinoma","umls","C1367774"
> "5591","eccrine papillary adenocarcinoma","mondo","0003531"
> "5593","gastric papillary adenocarcinoma","umls","C1333785"
> "5593","gastric papillary adenocarcinoma","mondo","0006228"
> "5592","breast papillary carcinoma","umls","C1336027"
> "5592","breast papillary carcinoma","mondo","0003532"
> "5595","papillary thymic adenocarcinoma","umls","C1335327"
> "5595","papillary thymic adenocarcinoma","mondo","0003534"
> "5597","fallopian tube papillary adenocarcinoma","umls","C1333595"
> "5597","fallopian tube papillary adenocarcinoma","mondo","0003535"
> "5598","fallopian tube serous adenocarcinoma","umls","C1517124"
> "5598","fallopian tube serous adenocarcinoma","mondo","0006208"
> "14450","46 XX gonadal dysgenesis","mesh","D023961"
> "14450","46 XX gonadal dysgenesis","umls","C0949595"
> "14450","46 XX gonadal dysgenesis","mondo","0009299"
> "0110159","Charcot-Marie-Tooth disease type 2B","icd10cm","G60.0"
> "0110159","Charcot-Marie-Tooth disease type 2B","mondo","0010949"
> "319","spinal cord disease","icd10cm","G95.9"
> "319","spinal cord disease","icd9cm","336.9"
> "319","spinal cord disease","mesh","D013118"
> "319","spinal cord disease","umls","C0037928"
> "319","spinal cord disease","mondo","0002545"
> "318","progressive muscular atrophy","icd9cm","335.21"
> "318","progressive muscular atrophy","mesh","D009134"
> "318","progressive muscular atrophy","umls","C0917981"
> "318","progressive muscular atrophy","mondo","0018687"
> "13690","acute gonococcal cystitis","icd9cm","098.11"
> "13690","acute gonococcal cystitis","umls","C0153191"
> "13690","acute gonococcal cystitis","mondo","0001777"
> "13691","dermoid cyst of skin","umls","C0349502"
> "13691","dermoid cyst of skin","mondo","0001778"
> "312","tenosynovitis of foot and ankle","icd9cm","727.06"
> "312","tenosynovitis of foot and ankle","umls","C0158331"
> "312","tenosynovitis of foot and ankle","mondo","0002517"
> "310","MERRF syndrome","icd10cm","E88.42"
> "310","MERRF syndrome","mesh","D017243"
> "310","MERRF syndrome","umls","C0162672"
> "310","MERRF syndrome","mondo","0010790"
> "315","synovium neoplasm","umls","C0476203"
> "315","synovium neoplasm","mondo","0002528"
> "314","tenosynovial giant cell tumor","icd9cm","727.02"
> "314","tenosynovial giant cell tumor","mesh","D000070779"
> "314","tenosynovial giant cell tumor","umls","C1318543"
> "314","tenosynovial giant cell tumor","mondo","0002522"
> "11201","parathyroid gland disease","icd10cm","E21.5"
> "11201","parathyroid gland disease","icd9cm","252"
> "11201","parathyroid gland disease","icd9cm","252.9"
> "11201","parathyroid gland disease","mesh","D010279"
> "11201","parathyroid gland disease","umls","C0030517"
> "11201","parathyroid gland disease","mondo","0001223"
> "11200","T cell deficiency","umls","C1274233"
> "11200","T cell deficiency","umls","C1333147"
> "11200","T cell deficiency","mondo","0001222"
> "11203","Angelucci's syndrome","icd10cm","H10.1"
> "11203","Angelucci's syndrome","icd9cm","372.05"
> "11203","Angelucci's syndrome","umls","C0001309"
> "11203","Angelucci's syndrome","mondo","0001224"
> "11202","primary hyperparathyroidism","icd10cm","E21.0"
> "11202","primary hyperparathyroidism","icd9cm","252.01"
> "11202","primary hyperparathyroidism","mesh","D049950"
> "11202","primary hyperparathyroidism","umls","C0221002"
> "11202","primary hyperparathyroidism","umls","C0271846"
> "11202","primary hyperparathyroidism","mondo","0010837"
> "11204","allergic conjunctivitis","mesh","D003233"
> "11204","allergic conjunctivitis","umls","C0009766"
> "11204","allergic conjunctivitis","mondo","0005642"
> "11206","opioid abuse","icd10cm","F11.1"
> "11206","opioid abuse","icd9cm","305.5"
> "11206","opioid abuse","mesh","D009293"
> "11206","opioid abuse","umls","C0029095"
> "11206","opioid abuse","mondo","0001225"
> "0111454","SHORT syndrome","mesh","C537327"
> "0111454","SHORT syndrome","umls","C0878684"
> "12225","Plica syndrome","icd10cm","M67.5"
> "12225","Plica syndrome","icd9cm","727.83"
> "12225","Plica syndrome","umls","C0878705"
> "12225","Plica syndrome","mondo","0001468"
> "12223","specific bursitis often of occupational origin","icd9cm","727.2"
> "12223","specific bursitis often of occupational origin","umls","C0158332"
> "12223","specific bursitis often of occupational origin","mondo","0001467"
> "12679","nephrocalcinosis","mesh","D009397"
> "12679","nephrocalcinosis","umls","C0027709"
> "12679","nephrocalcinosis","mondo","0001567"
> "0111456","Kaufman oculocerebrofacial syndrome","mesh","C537013"
> "0111456","Kaufman oculocerebrofacial syndrome","umls","C1855663"
> "2297","leptospirosis","icd10cm","A27"
> "2297","leptospirosis","icd10cm","A27.0"
> "2297","leptospirosis","icd10cm","A27.9"
> "2297","leptospirosis","icd9cm","100"
> "2297","leptospirosis","icd9cm","100.0"
> "2297","leptospirosis","icd9cm","100.9"
> "2297","leptospirosis","mesh","D007922"
> "2297","leptospirosis","mesh","D014895"
> "2297","leptospirosis","umls","C0023364"
> "2297","leptospirosis","umls","C0043102"
> "2297","leptospirosis","mondo","0005825"
> "6938","pediatric intraocular retinoblastoma","umls","C1321869"
> "6938","pediatric intraocular retinoblastoma","mondo","0004045"
> "6939","childhood brain meningioma","umls","C1332949"
> "6939","childhood brain meningioma","mondo","0004046"
> "10914","amnestic disorder","icd10cm","R41.3"
> "10914","amnestic disorder","icd9cm","294.0"
> "10914","amnestic disorder","mesh","D000647"
> "10914","amnestic disorder","umls","C0002622"
> "10914","amnestic disorder","umls","C0002625"
> "10914","amnestic disorder","mondo","0001152"
> "10915","Wernicke-Korsakoff syndrome","mesh","D020915"
> "10915","Wernicke-Korsakoff syndrome","umls","C0349464"
> "10915","Wernicke-Korsakoff syndrome","mondo","0010198"
> "10913","benign essential hypertension","icd9cm","401.1"
> "10913","benign essential hypertension","umls","C0155583"
> "10913","benign essential hypertension","mondo","0001151"
> "10919","transsexualism","icd9cm","302.50"
> "10919","transsexualism","mesh","D014189"
> "10919","transsexualism","umls","C0040630"
> "10919","transsexualism","mondo","0001153"
> "0070170","spermatogenic failure 19","mondo","0054723"
> "0070171","spermatogenic failure 12","mondo","0014172"
> "0070172","spermatogenic failure 15","mondo","0014847"
> "0070173","spermatogenic failure 7","mondo","0013070"
> "7922","benign mediastinal neurilemmoma","mondo","0004398"
> "0070176","spermatogenic failure 4","mondo","0010052"
> "0070177","spermatogenic failure 22","mondo","0054726"
> "0070178","spermatogenic failure 10","mondo","0013901"
> "0070179","spermatogenic failure 14","mondo","0014366"
> "9138","stomach carcinoma in situ","icd10cm","D00.2"
> "9138","stomach carcinoma in situ","icd9cm","230.2"
> "9138","stomach carcinoma in situ","umls","C0154060"
> "9138","stomach carcinoma in situ","mondo","0004716"
> "10314","endocarditis","icd10cm","I33.9"
> "10314","endocarditis","icd9cm","421.9"
> "10314","endocarditis","mesh","D004696"
> "10314","endocarditis","umls","C0014118"
> "10314","endocarditis","umls","C0375268"
> "10314","endocarditis","mondo","0005025"
> "7928","testis refractory cancer","umls","C1377904"
> "7928","testis refractory cancer","mondo","0004401"
> "6297","viral esophagitis","umls","C0341110"
> "6297","viral esophagitis","mondo","0003846"
> "6294","corpus callosum lipoma","umls","C1333160"
> "6294","corpus callosum lipoma","mondo","0003845"
> "6293","central nervous system lipoma","umls","C1332885"
> "6293","central nervous system lipoma","mondo","0003844"
> "6291","cerebral hemisphere lipoma","umls","C1332907"
> "6291","cerebral hemisphere lipoma","mondo","0003843"
> "7409","vulvar non-keratinizing squamous cell carcinoma","umls","C1520092"
> "7409","vulvar non-keratinizing squamous cell carcinoma","mondo","0004213"
> "0050156","idiopathic pulmonary fibrosis","icd10cm","J84.112"
> "0050156","idiopathic pulmonary fibrosis","icd9cm","516.31"
> "0050156","idiopathic pulmonary fibrosis","mesh","D054990"
> "0050156","idiopathic pulmonary fibrosis","umls","C1800706"
> "0050156","idiopathic pulmonary fibrosis","mondo","0008345"
> "0050157","cryptogenic organizing pneumonia","icd10cm","J84.116"
> "0050157","cryptogenic organizing pneumonia","icd9cm","516.36"
> "0050157","cryptogenic organizing pneumonia","mesh","D018549"
> "0050157","cryptogenic organizing pneumonia","umls","C0242770"
> "0050157","cryptogenic organizing pneumonia","mondo","0015264"
> "0050152","aspiration pneumonia","icd10cm","J69.0"
> "0050152","aspiration pneumonia","mesh","D011015"
> "0050152","aspiration pneumonia","umls","C0032290"
> "0050152","aspiration pneumonia","mondo","0000265"
> "7408","vulvar keratoacanthoma-like carcinoma","umls","C1520086"
> "7408","vulvar keratoacanthoma-like carcinoma","mondo","0004212"
> "0050158","desquamative interstitial pneumonia","icd10cm","J84.115"
> "0050158","desquamative interstitial pneumonia","icd10cm","J84.117"
> "0050158","desquamative interstitial pneumonia","icd9cm","516.34"
> "0050158","desquamative interstitial pneumonia","icd9cm","516.37"
> "0050158","desquamative interstitial pneumonia","mesh","C562470"
> "0050158","desquamative interstitial pneumonia","umls","C0238378"
> "0050158","desquamative interstitial pneumonia","mondo","0009887"
> "876","pyomyositis","icd10cm","M60.0"
> "876","pyomyositis","icd9cm","040.81"
> "876","pyomyositis","mesh","D052880"
> "876","pyomyositis","umls","C0041188"
> "876","pyomyositis","mondo","0019168"
> "3431","cerebritis","umls","C0742115"
> "3431","cerebritis","mondo","0002645"
> "874","bacterial pneumonia","icd10cm","J15.9"
> "874","bacterial pneumonia","icd9cm","482.9"
> "874","bacterial pneumonia","mesh","D018410"
> "874","bacterial pneumonia","umls","C0004626"
> "874","bacterial pneumonia","mondo","0004652"
> "873","anaerobic pneumonia","icd9cm","482.81"
> "873","anaerobic pneumonia","umls","C0375327"
> "873","anaerobic pneumonia","mondo","0004649"
> "870","neuropathy","icd10cm","G62.9"
> "870","neuropathy","umls","C0442874"
> "870","neuropathy","mondo","0005244"
> "3437","laryngitis","mesh","D007827"
> "3437","laryngitis","umls","C0023067"
> "3437","laryngitis","mondo","0002647"
> "2741","bilirubin metabolic disorder","mesh","D006932"
> "2741","bilirubin metabolic disorder","mesh","D006933"
> "2741","bilirubin metabolic disorder","umls","C0020433"
> "2741","bilirubin metabolic disorder","umls","C0020435"
> "2741","bilirubin metabolic disorder","mondo","0002408"
> "4593","pediatric meningioma","umls","C0280656"
> "4593","pediatric meningioma","mondo","0003057"
> "2743","pyeloureteritis cystica","icd10cm","N28.85"
> "2743","pyeloureteritis cystica","icd9cm","590.3"
> "2743","pyeloureteritis cystica","umls","C0156254"
> "2743","pyeloureteritis cystica","mondo","0002410"
> "4591","lymphoplasmacyte-rich meningioma","umls","C0431119"
> "4591","lymphoplasmacyte-rich meningioma","mondo","0003056"
> "2033","communication disorder","icd10cm","F80.9"
> "2033","communication disorder","mesh","D003147"
> "2033","communication disorder","umls","C0009460"
> "2033","communication disorder","mondo","0002182"
> "2744","pyelitis","icd10cm","N12"
> "2744","pyelitis","mesh","D011702"
> "2744","pyelitis","umls","C0034183"
> "2744","pyelitis","mondo","0006938"
> "4594","microcystic meningioma","mesh","D008579"
> "4594","microcystic meningioma","umls","C1384408"
> "4594","microcystic meningioma","mondo","0003058"
> "2030","anxiety disorder","icd10cm","F41.9"
> "2030","anxiety disorder","mesh","D001008"
> "2030","anxiety disorder","umls","C0003469"
> "2030","anxiety disorder","mondo","0005618"
> "4844","benign ependymoma","mesh","D004806"
> "4844","benign ependymoma","umls","C0014474"
> "4844","benign ependymoma","mondo","0003161"
> "4845","pilomyxoid astrocytoma","umls","C1519086"
> "4845","pilomyxoid astrocytoma","mondo","0016692"
> "4846","cauda equina intradural extramedullary astrocytoma","umls","C1334254"
> "4846","cauda equina intradural extramedullary astrocytoma","mondo","0003163"
> "4847","cauda equina neoplasm","umls","C1263892"
> "4847","cauda equina neoplasm","mondo","0003164"
> "4840","sebaceous carcinoma","icd10cm","C44"
> "4840","sebaceous carcinoma","umls","C1382026"
> "4840","sebaceous carcinoma","mondo","0006962"
> "0111249","uveal coloboma-cleft lip and palate-intellectual disability","umls","C0795902"
> "4843","subependymal glioma","mesh","D018315"
> "4843","subependymal glioma","umls","C0206725"
> "4843","subependymal glioma","mondo","0007667"
> "0110041","Alzheimer's disease 8","icd10cm","G30"
> "0110041","Alzheimer's disease 8","mondo","0011777"
> "0110040","Alzheimer's disease 4","mondo","0011743"
> "0110043","Alzheimer's disease 10","icd10cm","G30"
> "0110043","Alzheimer's disease 10","mondo","0012321"
> "0110045","Alzheimer's disease 12","icd10cm","G30"
> "0110045","Alzheimer's disease 12","mondo","0012609"
> "0110044","Alzheimer's disease 11","icd10cm","G30"
> "0110044","Alzheimer's disease 11","mondo","0012344"
> "0110047","Alzheimer's disease 14","icd10cm","G30"
> "0110047","Alzheimer's disease 14","mondo","0012631"
> "0110046","Alzheimer's disease 13","icd10cm","G30"
> "0110046","Alzheimer's disease 13","mondo","0012630"
> "0110049","Alzheimer's disease 17","mondo","0014036"
> "0110048","Alzheimer's disease 15","icd10cm","G30"
> "0110048","Alzheimer's disease 15","mondo","0012632"
> "0040003","benzylpenicillin allergy","umls","C0571411"
> "5200","urinary tract obstruction","icd10cm","N13.9"
> "5200","urinary tract obstruction","icd9cm","599.6"
> "5200","urinary tract obstruction","icd9cm","599.60"
> "5200","urinary tract obstruction","umls","C0178879"
> "5200","urinary tract obstruction","mondo","0003330"
> "0040006","carbamazepine allergy","umls","C0570787"
> "0040005","ceftriaxone allergy","umls","C0571463"
> "0040004","amoxicillin allergy","umls","C0571417"
> "5209","benign struma ovarii","umls","C1511104"
> "5209","benign struma ovarii","mondo","0003333"
> "5208","malignant struma ovarii","umls","C0334525"
> "5208","malignant struma ovarii","mondo","0003332"
> "0040009","lidocaine allergy","umls","C0570646"
> "0040008","isoniazide allergy","icd10cm","Z88.1"
> "11994","atrophy of testis","icd10cm","N50.0"
> "11994","atrophy of testis","icd9cm","608.3"
> "11994","atrophy of testis","umls","C0156312"
> "11994","atrophy of testis","mondo","0001415"
> "11997","spermatocele","icd10cm","N43.4"
> "11997","spermatocele","icd10cm","N43.40"
> "11997","spermatocele","icd10cm","N50.3"
> "11997","spermatocele","icd9cm","608.1"
> "11997","spermatocele","mesh","D013088"
> "11997","spermatocele","umls","C0037859"
> "11997","spermatocele","mondo","0006977"
> "11996","spermatic cord torsion","icd10cm","N44.0"
> "11996","spermatic cord torsion","icd10cm","N44.00"
> "11996","spermatic cord torsion","icd10cm","N44.02"
> "11996","spermatic cord torsion","icd9cm","608.2"
> "11996","spermatic cord torsion","icd9cm","608.20"
> "11996","spermatic cord torsion","mesh","D013086"
> "11996","spermatic cord torsion","umls","C0037856"
> "11996","spermatic cord torsion","mondo","0008541"
> "11695","portal vein thrombosis","icd10cm","I81"
> "11695","portal vein thrombosis","icd9cm","452"
> "11695","portal vein thrombosis","umls","C0155773"
> "11695","portal vein thrombosis","mondo","0001339"
> "12309","urticaria pigmentosa","icd10cm","D47.01"
> "12309","urticaria pigmentosa","mesh","D014582"
> "12309","urticaria pigmentosa","umls","C0042111"
> "12309","urticaria pigmentosa","mondo","0019316"
> "13413","hepatic encephalopathy","icd10cm","K72"
> "13413","hepatic encephalopathy","icd9cm","572.2"
> "13413","hepatic encephalopathy","mesh","D006501"
> "13413","hepatic encephalopathy","umls","C0019151"
> "13413","hepatic encephalopathy","mondo","0001711"
> "13174","dissociated nystagmus","icd10cm","H55.04"
> "13174","dissociated nystagmus","icd9cm","379.55"
> "13174","dissociated nystagmus","mesh","D009759"
> "13174","dissociated nystagmus","umls","C0155380"
> "13174","dissociated nystagmus","mondo","0001655"
> "12308","Dubin-Johnson syndrome","icd10cm","E80.6"
> "12308","Dubin-Johnson syndrome","mesh","D007566"
> "12308","Dubin-Johnson syndrome","umls","C0022350"
> "12308","Dubin-Johnson syndrome","mondo","0009380"
> "11190","pseudomembranous conjunctivitis","icd10cm","H10.22"
> "11190","pseudomembranous conjunctivitis","icd9cm","372.04"
> "11190","pseudomembranous conjunctivitis","umls","C0155144"
> "11190","pseudomembranous conjunctivitis","mondo","0001217"
> "11193","syndactyly","icd10cm","Q70"
> "11193","syndactyly","icd10cm","Q70.9"
> "11193","syndactyly","icd9cm","755.1"
> "11193","syndactyly","mesh","D013576"
> "11193","syndactyly","umls","C0039075"
> "11193","syndactyly","mondo","0021002"
> "11195","acute laryngopharyngitis","icd10cm","J06.0"
> "11195","acute laryngopharyngitis","icd9cm","465.0"
> "11195","acute laryngopharyngitis","umls","C0155817"
> "11195","acute laryngopharyngitis","mondo","0001218"
> "11197","serous conjunctivitis except viral","icd10cm","H10.23"
> "11197","serous conjunctivitis except viral","icd9cm","372.01"
> "11197","serous conjunctivitis except viral","umls","C0155142"
> "11197","serous conjunctivitis except viral","mondo","0001219"
> "11199","hypoparathyroidism","icd10cm","E20"
> "11199","hypoparathyroidism","icd10cm","E20.9"
> "11199","hypoparathyroidism","icd9cm","252.1"
> "11199","hypoparathyroidism","mesh","D007011"
> "11199","hypoparathyroidism","umls","C0020626"
> "11199","hypoparathyroidism","mondo","0001220"
> "11198","DiGeorge syndrome","icd10cm","D82.1"
> "11198","DiGeorge syndrome","icd9cm","279.11"
> "11198","DiGeorge syndrome","mesh","D004062"
> "11198","DiGeorge syndrome","umls","C0012236"
> "11198","DiGeorge syndrome","mondo","0008564"
> "3049","Churg-Strauss syndrome","icd10cm","M30.1"
> "3049","Churg-Strauss syndrome","mesh","D015267"
> "3049","Churg-Strauss syndrome","umls","C0008728"
> "3049","Churg-Strauss syndrome","mondo","0015943"
> "339","accessory nerve disease","icd9cm","352.4"
> "339","accessory nerve disease","mesh","D020436"
> "339","accessory nerve disease","umls","C0152180"
> "339","accessory nerve disease","mondo","0002636"
> "3042","allergic contact dermatitis","icd10cm","L23"
> "3042","allergic contact dermatitis","icd10cm","L23.9"
> "3042","allergic contact dermatitis","mesh","D017449"
> "3042","allergic contact dermatitis","umls","C0162820"
> "3042","allergic contact dermatitis","mondo","0006525"
> "3044","food allergy","mesh","D005512"
> "3044","food allergy","umls","C0016470"
> "3044","food allergy","mondo","0002497"
> "3047","Wissler's syndrome","mesh","D014924"
> "3047","Wissler's syndrome","umls","C0043195"
> "3047","Wissler's syndrome","mondo","0006018"
> "338","cranial nerve neoplasm","mesh","D003390"
> "338","cranial nerve neoplasm","umls","C0010267"
> "338","cranial nerve neoplasm","mondo","0002633"
> "1094","attention deficit hyperactivity disorder","mesh","D001289"
> "1094","attention deficit hyperactivity disorder","umls","C0041671"
> "1094","attention deficit hyperactivity disorder","mondo","0005302"
> "1091","tooth disease","mesh","D014076"
> "1091","tooth disease","umls","C0040435"
> "1091","tooth disease","mondo","0006999"
> "11671","hypotrichosis of eyelid","icd10cm","H02.72"
> "11671","hypotrichosis of eyelid","icd9cm","374.55"
> "11671","hypotrichosis of eyelid","umls","C0155214"
> "11671","hypotrichosis of eyelid","mondo","0001335"
> "1098","fetal erythroblastosis","icd10cm","P55"
> "1098","fetal erythroblastosis","icd10cm","P55.9"
> "1098","fetal erythroblastosis","icd9cm","773"
> "1098","fetal erythroblastosis","icd9cm","773.2"
> "1098","fetal erythroblastosis","mesh","D004899"
> "1098","fetal erythroblastosis","umls","C0014761"
> "1098","fetal erythroblastosis","mondo","0006760"
> "1099","alpha thalassemia","icd10cm","D56.0"
> "1099","alpha thalassemia","icd9cm","282.43"
> "1099","alpha thalassemia","mesh","D017085"
> "1099","alpha thalassemia","umls","C0002312"
> "1099","alpha thalassemia","mondo","0011399"
> "0060395","chromosome 15q24 deletion syndrome","icd10cm","Q93.5"
> "0060395","chromosome 15q24 deletion syndrome","mesh","C579849"
> "0060395","chromosome 15q24 deletion syndrome","mondo","0013256"
> "0060394","chromosome 15q13.3 microdeletion syndrome","icd10cm","Q93.5"
> "0060394","chromosome 15q13.3 microdeletion syndrome","mesh","C567439"
> "0060394","chromosome 15q13.3 microdeletion syndrome","mondo","0012774"
> "0060397","chromosome 15q26-qter deletion syndrome","icd10cm","Q93.5"
> "0060397","chromosome 15q26-qter deletion syndrome","mesh","C567232"
> "0060397","chromosome 15q26-qter deletion syndrome","mondo","0012964"
> "0060396","chromosome 15q25 deletion syndrome","mondo","0013672"
> "0060391","chromosome 13q14 deletion syndrome","icd10cm","Q93.5"
> "0060391","chromosome 13q14 deletion syndrome","mondo","0013481"
> "0060390","distal 10q deletion syndrome","icd10cm","Q93.5"
> "0060390","distal 10q deletion syndrome","mesh","C567182"
> "0060390","distal 10q deletion syndrome","mondo","0012315"
> "0060393","chromosome 15q11.2 deletion syndrome","mesh","C557830"
> "0060393","chromosome 15q11.2 deletion syndrome","umls","C3180937"
> "0060393","chromosome 15q11.2 deletion syndrome","mondo","0014294"
> "0060392","chromosome 14q11-q22 deletion syndrome","mondo","0013272"
> "0060399","chromosome 16p12.1 deletion syndrome, 520kb","mondo","0007631"
> "0060398","chromosome 16p11.2 deletion syndrome, 220kb","icd10cm","Q93.5"
> "0060398","chromosome 16p11.2 deletion syndrome, 220kb","mondo","0013267"
> "1324","lung cancer","icd10cm","C34.1"
> "1324","lung cancer","icd10cm","C34.2"
> "1324","lung cancer","icd10cm","C34.3"
> "1324","lung cancer","icd9cm","162.3"
> "1324","lung cancer","icd9cm","162.4"
> "1324","lung cancer","icd9cm","162.5"
> "1324","lung cancer","icd9cm","162.8"
> "1324","lung cancer","umls","C0024624"
> "1324","lung cancer","umls","C0153491"
> "1324","lung cancer","umls","C0153492"
> "1324","lung cancer","umls","C0153493"
> "1324","lung cancer","mondo","0008903"
> "1325","bronchus cancer","icd10cm","C34"
> "1325","bronchus cancer","icd10cm","C34.9"
> "1325","bronchus cancer","icd9cm","162.9"
> "1325","bronchus cancer","umls","C0348343"
> "1325","bronchus cancer","mondo","0001672"
> "1328","Rift Valley fever","icd10cm","A92.4"
> "1328","Rift Valley fever","mesh","D012295"
> "1328","Rift Valley fever","umls","C0035613"
> "1328","Rift Valley fever","mondo","0017880"
> "6451","central nervous system fibrosarcoma","umls","C1332879"
> "6451","central nervous system fibrosarcoma","mondo","0003882"
> "8683","myeloid sarcoma","icd10cm","C92.3"
> "8683","myeloid sarcoma","icd10cm","C92.30"
> "8683","myeloid sarcoma","icd9cm","205.3"
> "8683","myeloid sarcoma","mesh","D023981"
> "8683","myeloid sarcoma","umls","C0152276"
> "8683","myeloid sarcoma","mondo","0006861"
> "8680","alcoholic gastritis","icd10cm","K29.2"
> "8680","alcoholic gastritis","icd9cm","535.3"
> "8680","alcoholic gastritis","umls","C0156076"
> "8680","alcoholic gastritis","mondo","0004640"
> "8681","paraneoplastic polyneuropathy","icd9cm","357.3"
> "8681","paraneoplastic polyneuropathy","mesh","D020364"
> "8681","paraneoplastic polyneuropathy","umls","C0270932"
> "8681","paraneoplastic polyneuropathy","mondo","0006888"
> "8138","thymus sarcomatoid carcinoma","umls","C1335924"
> "8138","thymus sarcomatoid carcinoma","mondo","0006452"
> "8687","skin carcinoma in situ","icd10cm","D04"
> "8687","skin carcinoma in situ","icd10cm","D04.0"
> "8687","skin carcinoma in situ","icd10cm","D04.2"
> "8687","skin carcinoma in situ","icd10cm","D04.3"
> "8687","skin carcinoma in situ","icd10cm","D04.4"
> "8687","skin carcinoma in situ","icd10cm","D04.6"
> "8687","skin carcinoma in situ","icd10cm","D04.7"
> "8687","skin carcinoma in situ","icd10cm","D04.9"
> "8687","skin carcinoma in situ","icd9cm","232"
> "8687","skin carcinoma in situ","icd9cm","232.0"
> "8687","skin carcinoma in situ","icd9cm","232.2"
> "8687","skin carcinoma in situ","icd9cm","232.3"
> "8687","skin carcinoma in situ","icd9cm","232.4"
> "8687","skin carcinoma in situ","icd9cm","232.5"
> "8687","skin carcinoma in situ","icd9cm","232.6"
> "8687","skin carcinoma in situ","icd9cm","232.7"
> "8687","skin carcinoma in situ","icd9cm","232.9"
> "8687","skin carcinoma in situ","umls","C0154073"
> "8687","skin carcinoma in situ","umls","C0154074"
> "8687","skin carcinoma in situ","umls","C0154077"
> "8687","skin carcinoma in situ","umls","C0154078"
> "8687","skin carcinoma in situ","umls","C0154079"
> "8687","skin carcinoma in situ","umls","C0154080"
> "8687","skin carcinoma in situ","umls","C0154081"
> "8687","skin carcinoma in situ","umls","C0347139"
> "8687","skin carcinoma in situ","mondo","0004641"
> "6901","familiar ovarian carcinoma","umls","C1333992"
> "6901","familiar ovarian carcinoma","mondo","0004033"
> "6459","lipoma of the rectum","umls","C1335684"
> "6459","lipoma of the rectum","mondo","0003884"
> "8135","gallbladder lymphoma","umls","C1333748"
> "8135","gallbladder lymphoma","mondo","0004474"
> "8688","tonsillar pillar cancer","icd10cm","C09.1"
> "8688","tonsillar pillar cancer","icd9cm","146.2"
> "8688","tonsillar pillar cancer","umls","C0153385"
> "8688","tonsillar pillar cancer","mondo","0004642"
> "8137","thymus clear cell carcinoma","umls","C1333069"
> "8137","thymus clear cell carcinoma","mondo","0004475"
> "8130","breast columnar cell mucinous carcinoma","umls","C1511305"
> "8130","breast columnar cell mucinous carcinoma","mondo","0004472"
> "8133","epiglottis cancer","icd10cm","C10.1"
> "8133","epiglottis cancer","icd9cm","146.4"
> "8133","epiglottis cancer","umls","C0496765"
> "8133","epiglottis cancer","umls","C0585946"
> "8133","epiglottis cancer","umls","C1112382"
> "8133","epiglottis cancer","mondo","0004473"
> "0060170","generalized epilepsy with febrile seizures plus","icd10cm","G40.3"
> "0060170","generalized epilepsy with febrile seizures plus","mondo","0018214"
> "0060173","Timothy syndrome","icd10cm","G72.3"
> "0060173","Timothy syndrome","mesh","C536962"
> "0060173","Timothy syndrome","mondo","0010979"
> "0060175","succinic semialdehyde dehydrogenase deficiency","mesh","C535803"
> "0060175","succinic semialdehyde dehydrogenase deficiency","mondo","0010083"
> "0060174","GABA aminotransferase deficiency","mondo","0013166"
> "0060177","homocarnosinosis","mesh","C535328"
> "0060177","homocarnosinosis","mondo","0009351"
> "0060179","Renpenning syndrome","icd10cm","Q87.5"
> "0060179","Renpenning syndrome","mondo","0010653"
> "7732","childhood malignant schwannoma","umls","C0279987"
> "7732","childhood malignant schwannoma","mondo","0004345"
> "7731","childhood malignant hemangiopericytoma","umls","C0279983"
> "7731","childhood malignant hemangiopericytoma","mondo","0004344"
> "7736","retinal telangiectasia","icd9cm","362.15"
> "7736","retinal telangiectasia","umls","C0154835"
> "7736","retinal telangiectasia","mondo","0004348"
> "7735","pancreatic colloid cystadenoma","umls","C1335309"
> "7735","pancreatic colloid cystadenoma","mondo","0018523"
> "3953","adrenal gland cancer","icd10cm","C74"
> "3953","adrenal gland cancer","icd10cm","C74.9"
> "3953","adrenal gland cancer","icd9cm","194.0"
> "3953","adrenal gland cancer","mesh","D000310"
> "3953","adrenal gland cancer","umls","C0001624"
> "3953","adrenal gland cancer","umls","C0750887"
> "3953","adrenal gland cancer","mondo","0002817"
> "3952","adrenal cortex disease","mesh","D000303"
> "3952","adrenal cortex disease","umls","C0001614"
> "3952","adrenal cortex disease","mondo","0002816"
> "3951","acute myocarditis","icd10cm","I40"
> "3951","acute myocarditis","icd10cm","I40.9"
> "3951","acute myocarditis","icd9cm","422"
> "3951","acute myocarditis","icd9cm","422.90"
> "3951","acute myocarditis","umls","C0155686"
> "3951","acute myocarditis","mondo","0002815"
> "3950","adrenal carcinoma","umls","C1370740"
> "3950","adrenal carcinoma","mondo","0002814"
> "8358","pseudoglandular variant testicular seminoma","umls","C1515293"
> "8358","pseudoglandular variant testicular seminoma","mondo","0004541"
> "8352","aortic malignant tumor","umls","C1334560"
> "8352","aortic malignant tumor","mondo","0004539"
> "8353","epithelioid malignant peripheral nerve sheath tumor","umls","C1321427"
> "8353","epithelioid malignant peripheral nerve sheath tumor","mondo","0004540"
> "8354","complement component 3 deficiency","umls","C1332655"
> "8354","complement component 3 deficiency","mondo","0013417"
> "13839","extrapyramidal and movement disease","icd10cm","G20-G26"
> "13839","extrapyramidal and movement disease","icd10cm","G25.9"
> "13839","extrapyramidal and movement disease","icd9cm","333.90"
> "13839","extrapyramidal and movement disease","umls","C0477355"
> "13839","extrapyramidal and movement disease","mondo","0001815"
> "4062","testis sarcoma","umls","C1336727"
> "4062","testis sarcoma","mondo","0002861"
> "4060","breast rhabdomyosarcoma","umls","C1332637"
> "4060","breast rhabdomyosarcoma","mondo","0002859"
> "4061","testis rhabdomyosarcoma","umls","C1336726"
> "4061","testis rhabdomyosarcoma","mondo","0002860"
> "4066","anus rhabdomyosarcoma","umls","C1332276"
> "4066","anus rhabdomyosarcoma","mondo","0002864"
> "4067","anus sarcoma","umls","C1332277"
> "4067","anus sarcoma","mondo","0002865"
> "4064","bile duct sarcoma","umls","C2205442"
> "4064","bile duct sarcoma","mondo","0002862"
> "4065","mixed type rhabdomyosarcoma","umls","C0334481"
> "4065","mixed type rhabdomyosarcoma","mondo","0002863"
> "13778","chancroid","icd10cm","A57"
> "13778","chancroid","icd9cm","099.0"
> "13778","chancroid","mesh","D002602"
> "13778","chancroid","umls","C0007947"
> "13778","chancroid","mondo","0001797"
> "5784","esophageal neuroendocrine tumor","umls","C1333462"
> "5784","esophageal neuroendocrine tumor","mondo","0003649"
> "5781","atrophic flaccid tympanic membrane","icd10cm","H73.81"
> "5781","atrophic flaccid tympanic membrane","icd9cm","384.81"
> "5781","atrophic flaccid tympanic membrane","umls","C0155470"
> "5781","atrophic flaccid tympanic membrane","mondo","0003647"
> "5782","tympanic membrane disease","icd10cm","H73.9"
> "5782","tympanic membrane disease","icd10cm","H73.90"
> "5782","tympanic membrane disease","icd9cm","384.9"
> "5782","tympanic membrane disease","umls","C0041825"
> "5782","tympanic membrane disease","mondo","0003648"
> "5789","mixed hepatoblastoma","umls","C1334784"
> "5789","mixed hepatoblastoma","mondo","0003650"
> "3603","mucinous cystadenocarcinoma","mesh","D018282"
> "3603","mucinous cystadenocarcinoma","umls","C0206699"
> "3603","mucinous cystadenocarcinoma","mondo","0005858"
> "0080047","pseudoachondroplasia","mesh","C535819"
> "0080047","pseudoachondroplasia","mondo","0008322"
> "3606","ovarian mucinous adenocarcinoma","umls","C1335167"
> "3606","ovarian mucinous adenocarcinoma","mondo","0005601"
> "3609","breast mucinous cystadenocarcinoma","umls","C1511318"
> "3609","breast mucinous cystadenocarcinoma","mondo","0002705"
> "3608","appendix adenocarcinoma","umls","C0238003"
> "3608","appendix adenocarcinoma","mondo","0006087"
> "0050304","aniseikonia","mesh","D000839"
> "0050304","aniseikonia","mondo","0000309"
> "11432","endometriosis of ovary","icd10cm","N80.1"
> "11432","endometriosis of ovary","icd9cm","617.1"
> "11432","endometriosis of ovary","umls","C0156344"
> "11432","endometriosis of ovary","mondo","0006337"
> "11430","endometriosis in scar of skin","icd10cm","N80.6"
> "11430","endometriosis in scar of skin","icd9cm","617.6"
> "11430","endometriosis in scar of skin","umls","C0156348"
> "11430","endometriosis in scar of skin","mondo","0001287"
> "11431","endometriosis of rectovaginal septum and vagina","icd10cm","N80.4"
> "11431","endometriosis of rectovaginal septum and vagina","icd9cm","617.4"
> "11431","endometriosis of rectovaginal septum and vagina","umls","C0156346"
> "11431","endometriosis of rectovaginal septum and vagina","mondo","0001288"
> "4451","renal carcinoma","umls","C1378703"
> "4451","renal carcinoma","mondo","0005206"
> "4450","renal cell carcinoma","mesh","D002292"
> "4450","renal cell carcinoma","umls","C0007134"
> "4450","renal cell carcinoma","mondo","0005086"
> "4455","hereditary renal cell carcinoma","mondo","0003008"
> "4454","childhood kidney cell carcinoma","umls","C1333001"
> "4454","childhood kidney cell carcinoma","mondo","0003007"
> "13348","laryngeal cartilage cancer","icd10cm","C32.3"
> "13348","laryngeal cartilage cancer","icd9cm","161.3"
> "13348","laryngeal cartilage cancer","umls","C0153486"
> "13348","laryngeal cartilage cancer","mondo","0001691"
> "959","esophagus squamous cell papilloma","umls","C1333467"
> "959","esophagus squamous cell papilloma","mondo","0004827"
> "0090120","hereditary neutrophilia","mesh","C563010"
> "0090120","hereditary neutrophilia","umls","C0543669"
> "0090120","hereditary neutrophilia","mondo","0008092"
> "0090123","aromatic L-amino acid decarboxylase deficiency","umls","C1291564"
> "0090123","aromatic L-amino acid decarboxylase deficiency","mondo","0012084"
> "0090122","aromatase excess syndrome","icd10cm","E30.1"
> "0090122","aromatase excess syndrome","mondo","0007690"
> "0090125","COL4A1-related familial vascular leukoencephalopathy","mondo","0011865"
> "0090124","neurogenic arthrogryposis multiplex congenita","mesh","C536614"
> "0090124","neurogenic arthrogryposis multiplex congenita","umls","C1859721"
> "0090124","neurogenic arthrogryposis multiplex congenita","mondo","0008823"
> "0090127","camptodactyly-arthropathy-coxa vara-pericarditis syndrome","mesh","C537560"
> "0090127","camptodactyly-arthropathy-coxa vara-pericarditis syndrome","umls","C1859690"
> "0090127","camptodactyly-arthropathy-coxa vara-pericarditis syndrome","mondo","0008828"
> "0090126","branched-chain keto acid dehydrogenase kinase deficiency","icd10cm","E71.1"
> "0090126","branched-chain keto acid dehydrogenase kinase deficiency","mondo","0013970"
> "0090129","carnitine palmitoyltransferase I deficiency","icd10cm","E71.3"
> "0090129","carnitine palmitoyltransferase I deficiency","mondo","0009705"
> "950","dacryoadenitis","icd10cm","H04.0"
> "950","dacryoadenitis","icd10cm","H04.00"
> "950","dacryoadenitis","icd9cm","375.0"
> "950","dacryoadenitis","icd9cm","375.00"
> "950","dacryoadenitis","mesh","D003607"
> "950","dacryoadenitis","umls","C0155223"
> "950","dacryoadenitis","mondo","0004804"
> "952","acute dacryoadenitis","icd10cm","H04.01"
> "952","acute dacryoadenitis","icd9cm","375.01"
> "952","acute dacryoadenitis","umls","C0149505"
> "952","acute dacryoadenitis","mondo","0004812"
> "955","benign neurilemmoma","umls","C0854906"
> "955","benign neurilemmoma","mondo","0004818"
> "956","peripheral nerve schwannoma","umls","C1519001"
> "956","peripheral nerve schwannoma","mondo","0004820"
> "1762","cheilitis","icd10cm","K13.0"
> "1762","cheilitis","mesh","D002613"
> "1762","cheilitis","umls","C0007971"
> "1762","cheilitis","mondo","0002102"
> "0110676","congenital myasthenic syndrome 13","mondo","0013883"
> "0110677","congenital myasthenic syndrome 4B","mondo","0014586"
> "0070099","oculocutaneous albinism type V","mondo","0014127"
> "0070098","oculocutaneous albinism type IV","mondo","0011683"
> "0110672","congenital myasthenic syndrome 21","mondo","0014983"
> "0110673","congenital myasthenic syndrome 19","mondo","0014745"
> "0110670","congenital myasthenic syndrome 9","mondo","0014587"
> "0110671","congenital myasthenic syndrome 6","mondo","0009689"
> "0070093","schizophrenia 18","mondo","0014092"
> "0070092","schizophrenia 16","mondo","0013506"
> "0070091","schizophrenia 15","mondo","0013498"
> "0070090","schizophrenia 14","mondo","0012879"
> "0070097","oculocutaneous albinism type III","mondo","0008747"
> "0070096","oculocutaneous albinism type II","mondo","0008746"
> "0070095","oculocutaneous albinism type IB","mondo","0011749"
> "0070094","oculocutaneous albinism type IA","mondo","0008745"
> "6334","anterior optic tract meningioma","umls","C1332308"
> "6334","anterior optic tract meningioma","mondo","0003858"
> "6335","bilateral meningioma of optic nerve","mesh","C000608854"
> "6335","bilateral meningioma of optic nerve","umls","C1332551"
> "6335","bilateral meningioma of optic nerve","mondo","0003859"
> "12167","secondary vitreoretinal degeneration","icd10cm","H35.46"
> "12167","secondary vitreoretinal degeneration","icd9cm","362.66"
> "12167","secondary vitreoretinal degeneration","umls","C0154859"
> "12167","secondary vitreoretinal degeneration","mondo","0001457"
> "6337","cerebellopontine angle meningioma","umls","C1263882"
> "6337","cerebellopontine angle meningioma","mondo","0003860"
> "12161","peripheral retinal degeneration","icd10cm","H35.4"
> "12161","peripheral retinal degeneration","icd10cm","H35.40"
> "12161","peripheral retinal degeneration","icd9cm","362.6"
> "12161","peripheral retinal degeneration","icd9cm","362.60"
> "12161","peripheral retinal degeneration","umls","C1320640"
> "12161","peripheral retinal degeneration","mondo","0001451"
> "6331","immature teratoma of ovary","umls","C0346182"
> "6331","immature teratoma of ovary","mondo","0018369"
> "6332","adult malignant hemangiopericytoma","umls","C0279547"
> "6332","adult malignant hemangiopericytoma","mondo","0003856"
> "6333","adult intracranial malignant hemangiopericytoma","umls","C1334558"
> "6333","adult intracranial malignant hemangiopericytoma","mondo","0003857"
> "12169","carpal tunnel syndrome","icd10cm","G56.0"
> "12169","carpal tunnel syndrome","icd10cm","G56.00"
> "12169","carpal tunnel syndrome","icd9cm","354.0"
> "12169","carpal tunnel syndrome","mesh","D002349"
> "12169","carpal tunnel syndrome","umls","C0007286"
> "12169","carpal tunnel syndrome","mondo","0007275"
> "6339","vulvar eccrine adenocarcinoma","mondo","0003861"
> "0111507","Lenz-Majewski hyperostotic dwarfism","mesh","C537115"
> "0111507","Lenz-Majewski hyperostotic dwarfism","umls","C0432269"
> "0111506","palmoplantar keratoderma-esophageal carcinoma syndrome","mesh","C536164"
> "0111506","palmoplantar keratoderma-esophageal carcinoma syndrome","umls","C1835664"
> "0111505","palmoplantar keratoderma-deafness syndrome","mesh","C536152"
> "0111505","palmoplantar keratoderma-deafness syndrome","umls","C1835672"
> "0111509","lymphedema-distichiasis syndrome","mesh","C537710"
> "0111509","lymphedema-distichiasis syndrome","umls","C0265345"
> "0111508","Torrance type platyspondylic dysplasia","mesh","C563627"
> "0111508","Torrance type platyspondylic dysplasia","umls","C1835437"
> "9675","pulmonary emphysema","icd10cm","J43.8"
> "9675","pulmonary emphysema","icd9cm","492.8"
> "9675","pulmonary emphysema","mesh","D011656"
> "9675","pulmonary emphysema","umls","C0029607"
> "9675","pulmonary emphysema","mondo","0004849"
> "0070321","miliaria crystallina","icd10cm","L74.1"
> "10456","tonsillitis","icd10cm","J35.01"
> "10456","tonsillitis","icd9cm","474.00"
> "10456","tonsillitis","mesh","D014069"
> "10456","tonsillitis","umls","C0040425"
> "10456","tonsillitis","umls","C0149517"
> "10456","tonsillitis","mondo","0001039"
> "9672","noma","icd10cm","A69.0"
> "9672","noma","icd9cm","528.1"
> "9672","noma","mesh","D009625"
> "9672","noma","umls","C0028271"
> "9672","noma","mondo","0017124"
> "9673","ulcerative stomatitis","icd10cm","K12.1"
> "9673","ulcerative stomatitis","mesh","D005892"
> "9673","ulcerative stomatitis","umls","C0038367"
> "9673","ulcerative stomatitis","mondo","0004848"
> "10459","common cold","icd10cm","J00"
> "10459","common cold","icd9cm","460"
> "10459","common cold","mesh","D003139"
> "10459","common cold","umls","C0009443"
> "10459","common cold","mondo","0005709"
> "10458","legionellosis","mesh","D007876"
> "10458","legionellosis","umls","C0023240"
> "10458","legionellosis","mondo","0005823"
> "0070328","adult hepatocellular carcinoma","umls","C0279607"
> "0110452","dilated cardiomyopathy 1T","icd10cm","I42.0"
> "0110452","dilated cardiomyopathy 1T","mondo","0000911"
> "0110453","dilated cardiomyopathy 1EE","icd10cm","I42.0"
> "0110453","dilated cardiomyopathy 1EE","mondo","0013198"
> "0110450","dilated cardiomyopathy 1II","icd10cm","I42.0"
> "0110450","dilated cardiomyopathy 1II","mondo","0014073"
> "0110451","dilated cardiomyopathy 1O","icd10cm","I42.0"
> "0110451","dilated cardiomyopathy 1O","mondo","0012062"
> "0110456","dilated cardiomyopathy 1R","icd10cm","I42.0"
> "0110456","dilated cardiomyopathy 1R","mondo","0013261"
> "0110457","dilated cardiomyopathy 1Y","icd10cm","I42.0"
> "0110457","dilated cardiomyopathy 1Y","mondo","0012744"
> "0110454","dilated cardiomyopathy 1S","icd10cm","I42.0"
> "0110454","dilated cardiomyopathy 1S","mondo","0013262"
> "0110455","dilated cardiomyopathy 1U","icd10cm","I42.0"
> "0110455","dilated cardiomyopathy 1U","mondo","0013371"
> "0110458","dilated cardiomyopathy 1BB","icd10cm","I42.0"
> "0110458","dilated cardiomyopathy 1BB","mondo","0013030"
> "0110459","dilated cardiomyopathy 1FF","icd10cm","I42.0"
> "0110459","dilated cardiomyopathy 1FF","mondo","0013211"
> "12096","sodoku disease","icd10cm","A25.0"
> "12096","sodoku disease","icd9cm","026.0"
> "12096","sodoku disease","mesh","D011906"
> "12096","sodoku disease","umls","C0152062"
> "12096","sodoku disease","mondo","0020532"
> "0111213","distal spinal muscular atrophy type 4","umls","C1970211"
> "11850","transient refractive change","icd9cm","367.81"
> "11850","transient refractive change","umls","C0155000"
> "11850","transient refractive change","mondo","0001390"
> "11851","indeterminate leprosy","icd10cm","A30.0"
> "11851","indeterminate leprosy","icd9cm","030.2"
> "11851","indeterminate leprosy","umls","C0021192"
> "11851","indeterminate leprosy","mondo","0001391"
> "11853","monocular exotropia","icd10cm","H50.11"
> "11853","monocular exotropia","icd9cm","378.11"
> "11853","monocular exotropia","mesh","D005099"
> "11853","monocular exotropia","umls","C0152206"
> "11853","monocular exotropia","mondo","0001392"
> "4969","Gerstmann syndrome","mesh","D005862"
> "4969","Gerstmann syndrome","umls","C0017494"
> "4969","Gerstmann syndrome","mondo","0005773"
> "7127","radiation cystitis","icd10cm","N30.4"
> "7127","radiation cystitis","icd9cm","595.82"
> "7127","radiation cystitis","umls","C0156270"
> "7127","radiation cystitis","mondo","0004112"
> "1664","pineoblastoma","mesh","D010871"
> "1664","pineoblastoma","umls","C0205898"
> "1664","pineoblastoma","mondo","0016722"
> "1660","malignant pineal area germ cell neoplasm","umls","C0349621"
> "1660","malignant pineal area germ cell neoplasm","umls","C1334612"
> "1660","malignant pineal area germ cell neoplasm","mondo","0002073"
> "591","phobic disorder","icd10cm","F40"
> "591","phobic disorder","icd10cm","F40.9"
> "591","phobic disorder","icd9cm","300.2"
> "591","phobic disorder","icd9cm","300.20"
> "591","phobic disorder","mesh","D010698"
> "591","phobic disorder","umls","C0349231"
> "591","phobic disorder","mondo","0003699"
> "593","agoraphobia","icd10cm","F40.0"
> "593","agoraphobia","icd10cm","F40.00"
> "593","agoraphobia","mesh","D000379"
> "593","agoraphobia","umls","C0001818"
> "593","agoraphobia","mondo","0003709"
> "594","panic disorder","icd10cm","F41.0"
> "594","panic disorder","mesh","D016584"
> "594","panic disorder","umls","C0030319"
> "594","panic disorder","mondo","0005383"
> "599","specific phobia","icd10cm","F40.2"
> "599","specific phobia","mesh","C562465"
> "599","specific phobia","umls","C0236801"
> "599","specific phobia","mondo","0012000"
> "13760","Pthirus pubis infestation","icd10cm","B85.3"
> "13760","Pthirus pubis infestation","icd9cm","132.2"
> "13760","Pthirus pubis infestation","umls","C0030759"
> "13760","Pthirus pubis infestation","mondo","0001794"
> "2828","acalculous cholecystitis","mesh","D042101"
> "2828","acalculous cholecystitis","umls","C0267841"
> "2828","acalculous cholecystitis","mondo","0006633"
> "2825","nose disease","mesh","D009668"
> "2825","nose disease","umls","C0028432"
> "2825","nose disease","mondo","0002436"
> "5414","lung occult small cell carcinoma","umls","C1335099"
> "5414","lung occult small cell carcinoma","mondo","0003437"
> "3385","bacterial vaginosis","mesh","D016585"
> "3385","bacterial vaginosis","umls","C0085166"
> "3385","bacterial vaginosis","mondo","0005316"
> "0050958","spinocerebellar ataxia type 7","mondo","0008120"
> "0050959","spinocerebellar ataxia type 8","mondo","0012116"
> "3381","liposarcoma of bone","umls","C1332581"
> "3381","liposarcoma of bone","mondo","0002634"
> "0050954","spinocerebellar ataxia type 1","mondo","0008119"
> "0050955","spinocerebellar ataxia type 2","mondo","0008458"
> "0050956","spinocerebellar ataxia type 6","mondo","0008457"
> "14757","type III Ehlers-Danlos syndrome","mesh","C536196"
> "14757","type III Ehlers-Danlos syndrome","umls","C0268337"
> "14757","type III Ehlers-Danlos syndrome","mondo","0007523"
> "5418","schizoaffective disorder","icd10cm","F25"
> "5418","schizoaffective disorder","icd10cm","F25.9"
> "5418","schizoaffective disorder","icd9cm","295.7"
> "5418","schizoaffective disorder","mesh","D011618"
> "5418","schizoaffective disorder","umls","C0036337"
> "5418","schizoaffective disorder","mondo","0005487"
> "5419","schizophrenia","icd10cm","F20"
> "5419","schizophrenia","icd10cm","F20.9"
> "5419","schizophrenia","icd9cm","295"
> "5419","schizophrenia","icd9cm","295.9"
> "5419","schizophrenia","icd9cm","295.90"
> "5419","schizophrenia","mesh","D012559"
> "5419","schizophrenia","umls","C0036341"
> "5419","schizophrenia","mondo","0005090"
> "3388","periodontal disease","icd10cm","K05.6"
> "3388","periodontal disease","mesh","D010510"
> "3388","periodontal disease","umls","C0031090"
> "3388","periodontal disease","mondo","0002635"
> "3389","Papillon-Lefevre disease","mesh","D010214"
> "3389","Papillon-Lefevre disease","umls","C0030360"
> "3389","Papillon-Lefevre disease","mondo","0009490"
> "0080390","nephrotic syndrome type 1","mesh","C535761"
> "0080390","nephrotic syndrome type 1","umls","C0403399"
> "1400","lacrimal apparatus disease","icd10cm","H04"
> "1400","lacrimal apparatus disease","icd10cm","H04.9"
> "1400","lacrimal apparatus disease","icd9cm","375"
> "1400","lacrimal apparatus disease","icd9cm","375.9"
> "1400","lacrimal apparatus disease","mesh","D007766"
> "1400","lacrimal apparatus disease","umls","C0022904"
> "1400","lacrimal apparatus disease","mondo","0001854"
> "1407","anterior uveitis","mesh","D014606"
> "1407","anterior uveitis","umls","C0042165"
> "1407","anterior uveitis","mondo","0006651"
> "1406","iritis","mesh","D007500"
> "1406","iritis","umls","C0022081"
> "1406","iritis","mondo","0006814"
> "1405","primary angle-closure glaucoma","icd10cm","H40.2"
> "1405","primary angle-closure glaucoma","icd10cm","H40.20"
> "1405","primary angle-closure glaucoma","icd9cm","365.2"
> "1405","primary angle-closure glaucoma","icd9cm","365.20"
> "1405","primary angle-closure glaucoma","umls","C0017606"
> "1405","primary angle-closure glaucoma","mondo","0001868"
> "1404","residual stage angle-closure glaucoma","icd10cm","H40.24"
> "1404","residual stage angle-closure glaucoma","icd9cm","365.24"
> "1404","residual stage angle-closure glaucoma","umls","C0154948"
> "1404","residual stage angle-closure glaucoma","mondo","0001864"
> "4217","malignant ovarian Brenner tumor","mesh","D001948"
> "4217","malignant ovarian Brenner tumor","umls","C0334495"
> "4217","malignant ovarian Brenner tumor","mondo","0002920"
> "4211","posterior cranial fossa meningioma","umls","C1335448"
> "4211","posterior cranial fossa meningioma","mondo","0002919"
> "4210","clear cell meningioma","mesh","D008579"
> "4210","clear cell meningioma","umls","C0431121"
> "4210","clear cell meningioma","mondo","0002918"
> "13902","white piedra","icd10cm","B36.2"
> "13902","white piedra","icd9cm","111.2"
> "13902","white piedra","mesh","D010854"
> "13902","white piedra","umls","C0031898"
> "13902","white piedra","umls","C0040249"
> "13902","white piedra","mondo","0001827"
> "13909","red-green color blindness","icd10cm","H53.53"
> "13909","red-green color blindness","icd9cm","368.52"
> "13909","red-green color blindness","mesh","D003117"
> "13909","red-green color blindness","umls","C0155016"
> "13909","red-green color blindness","mondo","0010564"
> "10783","methemoglobinemia","icd10cm","D74"
> "10783","methemoglobinemia","icd10cm","D74.9"
> "10783","methemoglobinemia","icd9cm","289.7"
> "10783","methemoglobinemia","mesh","D008708"
> "10783","methemoglobinemia","umls","C0025637"
> "10783","methemoglobinemia","mondo","0001117"
> "5579","gastric gastrinoma","umls","C1333767"
> "5579","gastric gastrinoma","mondo","0003524"
> "10782","mesenteric lymphadenitis","icd10cm","I88.0"
> "10782","mesenteric lymphadenitis","icd9cm","289.2"
> "10782","mesenteric lymphadenitis","mesh","D008640"
> "10782","mesenteric lymphadenitis","umls","C0025469"
> "10782","mesenteric lymphadenitis","mondo","0001116"
> "5577","gastrinoma","mesh","D015408"
> "5577","gastrinoma","umls","C0017150"
> "5577","gastrinoma","mondo","0003523"
> "5576","inhibited male orgasm","icd10cm","F52.32"
> "5576","inhibited male orgasm","umls","C0033949"
> "5576","inhibited male orgasm","mondo","0003522"
> "5574","VIPoma","mesh","D003969"
> "5574","VIPoma","umls","C0011993"
> "5574","VIPoma","mondo","0019960"
> "5572","Beckwith-Wiedemann syndrome","icd10cm","Q87.3"
> "5572","Beckwith-Wiedemann syndrome","mesh","D001506"
> "5572","Beckwith-Wiedemann syndrome","umls","C0004903"
> "5572","Beckwith-Wiedemann syndrome","mondo","0007534"
> "5570","malignant acrospiroma","umls","C1260964"
> "5570","malignant acrospiroma","mondo","0024245"
> "0070216","familial hyperinsulinemic hypoglycemia 3","mondo","0011236"
> "5128","deep leiomyoma","umls","C1333266"
> "5128","deep leiomyoma","mondo","0003289"
> "3969","thyroid gland papillary carcinoma","mesh","C536915"
> "3969","thyroid gland papillary carcinoma","umls","C0238463"
> "3969","thyroid gland papillary carcinoma","mondo","0005075"
> "3264","subacute leukemia","icd9cm","208.2"
> "3264","subacute leukemia","umls","C0153924"
> "3264","subacute leukemia","mondo","0002582"
> "0060614","ulnar-mammary syndrome","mesh","C536937"
> "0060614","ulnar-mammary syndrome","umls","C1866994"
> "0060614","ulnar-mammary syndrome","mondo","0008411"
> "0080050","acromesomelic dysplasia, Maroteaux type","mesh","C535661"
> "0080050","acromesomelic dysplasia, Maroteaux type","mondo","0011275"
> "14472","hantavirus pulmonary syndrome","mesh","D018804"
> "14472","hantavirus pulmonary syndrome","umls","C0243025"
> "14472","hantavirus pulmonary syndrome","mondo","0017879"
> "0060610","megacystis-microcolon-intestinal hypoperistalsis syndrome","mesh","C536138"
> "0060610","megacystis-microcolon-intestinal hypoperistalsis syndrome","umls","C1608393"
> "0060610","megacystis-microcolon-intestinal hypoperistalsis syndrome","mondo","0007960"
> "0060611","abdominal obesity-metabolic syndrome","mondo","0000816"
> "0060612","abdominal obesity-metabolic syndrome 3","mondo","0014352"
> "0060613","X-linked cleft palate with or without ankyloglossia","mondo","0017938"
> "334","histrionic personality disorder","icd10cm","F60.4"
> "334","histrionic personality disorder","icd9cm","301.5"
> "334","histrionic personality disorder","icd9cm","301.50"
> "334","histrionic personality disorder","mesh","D006677"
> "334","histrionic personality disorder","umls","C0019681"
> "334","histrionic personality disorder","mondo","0002613"
> "337","spinal accessory nerve neoplasm","umls","C1263902"
> "337","spinal accessory nerve neoplasm","mondo","0002626"
> "331","central nervous system disease","icd10cm","G96.9"
> "331","central nervous system disease","mesh","D002493"
> "331","central nervous system disease","umls","C0007682"
> "331","central nervous system disease","mondo","0002602"
> "332","amyotrophic lateral sclerosis","kegg","05014"
> "332","amyotrophic lateral sclerosis","icd10cm","G12.21"
> "332","amyotrophic lateral sclerosis","icd9cm","335.20"
> "332","amyotrophic lateral sclerosis","mesh","D000690"
> "332","amyotrophic lateral sclerosis","umls","C0002736"
> "332","amyotrophic lateral sclerosis","mondo","0004976"
> "5124","fallopian tube leiomyoma","umls","C1517115"
> "5124","fallopian tube leiomyoma","mondo","0003285"
> "11227","acute hemorrhagic conjunctivitis","icd9cm","077.4"
> "11227","acute hemorrhagic conjunctivitis","mesh","D003232"
> "11227","acute hemorrhagic conjunctivitis","umls","C0009765"
> "11227","acute hemorrhagic conjunctivitis","mondo","0005634"
> "0080054","achondrogenesis type IA","mondo","0008701"
> "11223","small intestine diverticulitis","icd9cm","562.02"
> "11223","small intestine diverticulitis","umls","C0156164"
> "11223","small intestine diverticulitis","mondo","0001229"
> "0080055","achondrogenesis type IB","mondo","0010966"
> "0080056","achondrogenesis type II","mondo","0008702"
> "10031","compensatory emphysema","icd10cm","J98.3"
> "10031","compensatory emphysema","icd9cm","518.2"
> "10031","compensatory emphysema","umls","C0155918"
> "10031","compensatory emphysema","mondo","0000924"
> "10030","interstitial emphysema","icd10cm","J98.2"
> "10030","interstitial emphysema","icd9cm","518.1"
> "10030","interstitial emphysema","umls","C1370824"
> "10030","interstitial emphysema","mondo","0000923"
> "0080059","autosomal recessive spinocerebellar ataxia 7","mondo","0012235"
> "3635","congenital myasthenic syndrome","mesh","D020294"
> "3635","congenital myasthenic syndrome","umls","C0751882"
> "3635","congenital myasthenic syndrome","mondo","0018940"
> "0110520","autosomal recessive nonsyndromic deafness 7","icd10cm","H90.3"
> "0110520","autosomal recessive nonsyndromic deafness 7","mondo","0010967"
> "0110521","autosomal recessive nonsyndromic deafness 70","icd10cm","H90.3"
> "0110521","autosomal recessive nonsyndromic deafness 70","mondo","0013978"
> "0060246","MASA syndrome","mesh","C536029"
> "0060246","MASA syndrome","umls","C0795953"
> "0060246","MASA syndrome","mondo","0010559"
> "0060245","Mast syndrome","icd10cm","G11.4"
> "0060245","Mast syndrome","mesh","C565409"
> "0060245","Mast syndrome","mondo","0009568"
> "0111211","distal spinal muscular atrophy type 3","umls","C1846823"
> "0110528","autosomal recessive nonsyndromic deafness 83","icd10cm","H90.3"
> "0110528","autosomal recessive nonsyndromic deafness 83","mondo","0013365"
> "0050528","nonphotosensitive trichothiodystrophy","mondo","0021013"
> "12759","choroid cancer","icd10cm","C69.3"
> "12759","choroid cancer","icd9cm","190.6"
> "12759","choroid cancer","mesh","D002830"
> "12759","choroid cancer","umls","C0008523"
> "12759","choroid cancer","umls","C0153630"
> "12759","choroid cancer","mondo","0006700"
> "12756","lacrimal duct cancer","icd9cm","190.7"
> "12756","lacrimal duct cancer","umls","C0153631"
> "12756","lacrimal duct cancer","mondo","0001580"
> "6103","thoracic spinal canal and spinal cord meningioma","umls","C1336738"
> "6103","thoracic spinal canal and spinal cord meningioma","mondo","0003770"
> "6102","herpetic gastritis","umls","C1333996"
> "6102","herpetic gastritis","mondo","0003769"
> "6101","signet ring cell variant cervical mucinous adenocarcinoma","umls","C1516424"
> "6101","signet ring cell variant cervical mucinous adenocarcinoma","mondo","0003768"
> "13239","internal pathological resorption","icd9cm","521.41"
> "13239","internal pathological resorption","umls","C1456167"
> "13239","internal pathological resorption","mondo","0001668"
> "10938","paranoid personality disorder","icd10cm","F60.0"
> "10938","paranoid personality disorder","icd9cm","301.0"
> "10938","paranoid personality disorder","mesh","D010260"
> "10938","paranoid personality disorder","umls","C0030477"
> "10938","paranoid personality disorder","mondo","0001163"
> "10939","antisocial personality disorder","icd10cm","F60.2"
> "10939","antisocial personality disorder","icd9cm","301.7"
> "10939","antisocial personality disorder","mesh","D000987"
> "10939","antisocial personality disorder","umls","C0003431"
> "10939","antisocial personality disorder","mondo","0001164"
> "10934","multiple personality disorder","icd10cm","F44.81"
> "10934","multiple personality disorder","icd9cm","300.14"
> "10934","multiple personality disorder","mesh","D009105"
> "10934","multiple personality disorder","umls","C0026773"
> "10934","multiple personality disorder","mondo","0001159"
> "10935","dissociative disorder","icd10cm","F44.9"
> "10935","dissociative disorder","icd10cm","F48.9"
> "10935","dissociative disorder","icd9cm","300.15"
> "10935","dissociative disorder","icd9cm","300.9"
> "10935","dissociative disorder","mesh","D004213"
> "10935","dissociative disorder","umls","C0012746"
> "10935","dissociative disorder","umls","C0041857"
> "10935","dissociative disorder","mondo","0001160"
> "10936","schizoid personality disorder","icd10cm","F60.1"
> "10936","schizoid personality disorder","icd9cm","301.2"
> "10936","schizoid personality disorder","icd9cm","301.20"
> "10936","schizoid personality disorder","mesh","D012557"
> "10936","schizoid personality disorder","umls","C0036339"
> "10936","schizoid personality disorder","mondo","0001161"
> "10937","impulse control disorder","icd10cm","F63.9"
> "10937","impulse control disorder","icd9cm","312.30"
> "10937","impulse control disorder","mesh","D007174"
> "10937","impulse control disorder","umls","C0021122"
> "10937","impulse control disorder","mondo","0001162"
> "10930","borderline personality disorder","icd10cm","F60.3"
> "10930","borderline personality disorder","icd9cm","301.83"
> "10930","borderline personality disorder","mesh","D001883"
> "10930","borderline personality disorder","umls","C0006012"
> "10930","borderline personality disorder","mondo","0001156"
> "10931","dependent personality disorder","icd10cm","F60.7"
> "10931","dependent personality disorder","icd9cm","301.6"
> "10931","dependent personality disorder","mesh","D003859"
> "10931","dependent personality disorder","umls","C0011548"
> "10931","dependent personality disorder","mondo","0001157"
> "10932","obsessive-compulsive personality disorder","icd10cm","F60.5"
> "10932","obsessive-compulsive personality disorder","icd9cm","301.4"
> "10932","obsessive-compulsive personality disorder","mesh","D003193"
> "10932","obsessive-compulsive personality disorder","umls","C0009595"
> "10932","obsessive-compulsive personality disorder","mondo","0001158"
> "10933","obsessive-compulsive disorder","icd10cm","F42"
> "10933","obsessive-compulsive disorder","icd10cm","F42.8"
> "10933","obsessive-compulsive disorder","icd10cm","F42.9"
> "10933","obsessive-compulsive disorder","icd9cm","300.3"
> "10933","obsessive-compulsive disorder","mesh","D009771"
> "10933","obsessive-compulsive disorder","umls","C0028768"
> "10933","obsessive-compulsive disorder","mondo","0008114"
> "9119","acute myeloid leukemia","kegg","05221"
> "9119","acute myeloid leukemia","icd10cm","C92.0"
> "9119","acute myeloid leukemia","icd10cm","C92.00"
> "9119","acute myeloid leukemia","icd9cm","205.0"
> "9119","acute myeloid leukemia","mesh","D015470"
> "9119","acute myeloid leukemia","umls","C0023467"
> "9119","acute myeloid leukemia","mondo","0018874"
> "0070158","hereditary sensory neuropathy type 1E","icd10cm","G60.8"
> "0070158","hereditary sensory neuropathy type 1E","mondo","0013584"
> "0070159","hereditary sensory neuropathy X-linked","mondo","0010688"
> "0070152","hereditary sensory and autonomic neuropathy type 1A","mondo","0008086"
> "0070153","hereditary sensory and autonomic neuropathy type 8","mondo","0014662"
> "9113","granuloma inguinale","icd10cm","A58"
> "9113","granuloma inguinale","icd9cm","099.2"
> "9113","granuloma inguinale","mesh","D006100"
> "9113","granuloma inguinale","umls","C0018190"
> "9113","granuloma inguinale","mondo","0005777"
> "0070151","hereditary sensory and autonomic neuropathy type 6","icd10cm","G60.8"
> "0070151","hereditary sensory and autonomic neuropathy type 6","mondo","0013839"
> "0070156","hereditary sensory neuropathy type 1D","mondo","0013381"
> "9442","cervical Mullerian papilloma","umls","C1516427"
> "9442","cervical Mullerian papilloma","mondo","0004787"
> "0070154","hereditary sensory neuropathy type 1F","mondo","0014286"
> "0070155","hereditary sensory and autonomic neuropathy type 2A","mondo","0024309"
> "0050792","multiple cutaneous and mucosal venous malformations","mondo","0010842"
> "0050793","short QT syndrome","mondo","0000453"
> "0050790","fibular hypoplasia and complex brachydactyly","kegg","H00467"
> "0050790","fibular hypoplasia and complex brachydactyly","mesh","C537931"
> "0050790","fibular hypoplasia and complex brachydactyly","mondo","0009231"
> "0050791","persistent Mullerian duct syndrome","mesh","C536665"
> "0050791","persistent Mullerian duct syndrome","umls","C1849930"
> "0050791","persistent Mullerian duct syndrome","mondo","0009857"
> "0050796","achalasia microcephaly syndrome","mesh","C536010"
> "0050796","achalasia microcephaly syndrome","umls","C1860212"
> "0050796","achalasia microcephaly syndrome","mondo","0008699"
> "0050797","peroxisomal acyl-CoA oxidase deficiency","mesh","C536662"
> "0050797","peroxisomal acyl-CoA oxidase deficiency","umls","C1849678"
> "0050797","peroxisomal acyl-CoA oxidase deficiency","mondo","0009919"
> "0050794","multiple synostoses syndrome","mondo","0017923"
> "0050795","cone dystrophy","mondo","0000455"
> "0050799","guanidinoacetate methyltransferase deficiency","mesh","C537622"
> "0050799","guanidinoacetate methyltransferase deficiency","mondo","0012999"
> "1933","Rubinstein-Taybi syndrome","icd10cm","Q87.2"
> "1933","Rubinstein-Taybi syndrome","mesh","D012415"
> "1933","Rubinstein-Taybi syndrome","umls","C0035934"
> "1933","Rubinstein-Taybi syndrome","mondo","0019188"
> "0080188","chronic myelomonocytic leukemia","mondo","0020311"
> "0080187","chronic neutrophilic leukemia","mondo","0019451"
> "0080181","PHARC syndrome","mondo","0012984"
> "0111082","Fanconi anemia complementation group L","mondo","0013566"
> "0111083","Fanconi anemia complementation group D2","mondo","0009214"
> "0111080","Fanconi anemia complementation group V","mondo","0014985"
> "0111081","Fanconi anemia complementation group T","mondo","0014638"
> "0111086","Fanconi anemia complementation group G","mondo","0013565"
> "0111087","Fanconi anemia complementation group C","mondo","0009213"
> "0111084","Fanconi anemia complementation group E","mondo","0010953"
> "0111085","Fanconi anemia complementation group U","mondo","0014987"
> "0111088","Fanconi anemia complementation group F","mondo","0011325"
> "0111089","Fanconi anemia complementation group D1","mondo","0011584"
> "14221","abdominal obesity-metabolic syndrome 1","icd10cm","E88.81"
> "14221","abdominal obesity-metabolic syndrome 1","icd9cm","277.7"
> "14221","abdominal obesity-metabolic syndrome 1","mesh","D024821"
> "14221","abdominal obesity-metabolic syndrome 1","umls","C0524620"
> "14221","abdominal obesity-metabolic syndrome 1","mondo","0011565"
> "12753","corneal staphyloma","icd10cm","H18.72"
> "12753","corneal staphyloma","icd9cm","371.73"
> "12753","corneal staphyloma","umls","C0152440"
> "12753","corneal staphyloma","mondo","0001579"
> "3417","glossopharyngeal nerve neoplasm","umls","C1263900"
> "3417","glossopharyngeal nerve neoplasm","mondo","0002638"
> "14223","ochronosis","icd10cm","E70.29"
> "14223","ochronosis","mesh","D009794"
> "14223","ochronosis","umls","C0028817"
> "14223","ochronosis","mondo","0001910"
> "3413","alpha-mannosidosis","mesh","D008363"
> "3413","alpha-mannosidosis","umls","C0024748"
> "3413","alpha-mannosidosis","mondo","0009561"
> "3410","carotid artery thrombosis","mesh","D002341"
> "3410","carotid artery thrombosis","umls","C0007274"
> "3410","carotid artery thrombosis","mondo","0006690"
> "8023","myxoid liposarcoma of the ovary","umls","C1335170"
> "8023","myxoid liposarcoma of the ovary","mondo","0004436"
> "1931","hypothalamic disease","mesh","D007027"
> "1931","hypothalamic disease","umls","C0020655"
> "1931","hypothalamic disease","mondo","0002150"
> "0050175","tick-borne encephalitis","icd10cm","A84.1"
> "0050175","tick-borne encephalitis","icd9cm","063.2"
> "0050175","tick-borne encephalitis","mesh","D004675"
> "0050175","tick-borne encephalitis","umls","C0014054"
> "0050175","tick-borne encephalitis","mondo","0017572"
> "3418","glossopharyngeal nerve disease","icd10cm","G52"
> "3418","glossopharyngeal nerve disease","icd9cm","352"
> "3418","glossopharyngeal nerve disease","umls","C0154730"
> "3418","glossopharyngeal nerve disease","mondo","0002639"
> "3419","optic nerve neoplasm","mesh","D019574"
> "3419","optic nerve neoplasm","umls","C0524802"
> "3419","optic nerve neoplasm","mondo","0002640"
> "14228","oligospermia","icd10cm","N46.1"
> "14228","oligospermia","icd10cm","N46.11"
> "14228","oligospermia","icd9cm","606.1"
> "14228","oligospermia","mesh","D009845"
> "14228","oligospermia","umls","C0028960"
> "14228","oligospermia","mondo","0001913"
> "4868","prostate adenoid cystic carcinoma","umls","C1335502"
> "4868","prostate adenoid cystic carcinoma","mondo","0003177"
> "4869","laryngeal adenoid cystic carcinoma","umls","C1334368"
> "4869","laryngeal adenoid cystic carcinoma","mondo","0006264"
> "10660","mediastinum neuroblastoma","umls","C1334673"
> "10660","mediastinum neuroblastoma","mondo","0001095"
> "10661","mediastinum ganglioneuroblastoma","umls","C1334653"
> "10661","mediastinum ganglioneuroblastoma","mondo","0001096"
> "1930","Laurence-Moon syndrome","mesh","D007849"
> "1930","Laurence-Moon syndrome","umls","C0023138"
> "1930","Laurence-Moon syndrome","mondo","0009514"
> "13481","thanatophoric dysplasia","icd10cm","Q77.1"
> "13481","thanatophoric dysplasia","mesh","D013796"
> "13481","thanatophoric dysplasia","umls","C0039743"
> "13481","thanatophoric dysplasia","mondo","0017042"
> "4863","spinal cord astrocytoma","umls","C0349540"
> "4863","spinal cord astrocytoma","mondo","0003174"
> "4860","brain stem astrocytic neoplasm","umls","C1332608"
> "4860","brain stem astrocytic neoplasm","mondo","0003173"
> "8025","gastric signet ring cell adenocarcinoma","umls","C1335965"
> "8025","gastric signet ring cell adenocarcinoma","mondo","0006409"
> "4866","salivary gland adenoid cystic carcinoma","mesh","D003528"
> "4866","salivary gland adenoid cystic carcinoma","umls","C0010606"
> "4866","salivary gland adenoid cystic carcinoma","mondo","0003175"
> "4867","cervical adenoid cystic carcinoma","umls","C1332911"
> "4867","cervical adenoid cystic carcinoma","mondo","0006133"
> "13487","childhood disintegrative disease","icd10cm","F84.3"
> "13487","childhood disintegrative disease","icd9cm","299.1"
> "13487","childhood disintegrative disease","umls","C0236791"
> "13487","childhood disintegrative disease","mondo","0001726"
> "2012","Nezelof syndrome","icd10cm","D81.4"
> "2012","Nezelof syndrome","icd9cm","279.13"
> "2012","Nezelof syndrome","mesh","C536288"
> "2012","Nezelof syndrome","umls","C0152094"
> "2012","Nezelof syndrome","mondo","0009451"
> "0110029","alpha thalassemia-intellectual disability syndrome type 1","icd10cm","D56.0"
> "0110029","alpha thalassemia-intellectual disability syndrome type 1","mondo","0007716"
> "0110028","age related macular degeneration 5","mondo","0013409"
> "14107","De Quervain disease","icd10cm","M65.4"
> "14107","De Quervain disease","icd9cm","727.04"
> "14107","De Quervain disease","mesh","D053684"
> "14107","De Quervain disease","umls","C0149870"
> "14107","De Quervain disease","mondo","0006721"
> "0110023","age related macular degeneration 11","mondo","0012767"
> "0110022","age related macular degeneration 10","mondo","0012674"
> "0110021","age related macular degeneration 9","mondo","0012659"
> "0110020","age related macular degeneration 8","mondo","0013416"
> "0110027","age related macular degeneration 15","mondo","0014266"
> "0110026","age related macular degeneration 14","mondo","0014207"
> "0110025","age related macular degeneration 13","mondo","0014189"
> "0110024","age related macular degeneration 12","mondo","0013420"
> "0040029","trimethoprim allergy","umls","C0571390"
> "0040028","succinylcholine allergy","umls","C0571140"
> "0040025","cefuroxime allergy","umls","C0571454"
> "0040024","ceftazidime allergy","umls","C0571458"
> "0040027","cyclophosphamide allergy","umls","C0570670"
> "0040026","chlorhexidine allergy","umls","C0571344"
> "0040021","cephalosporin allergy","umls","C0571444"
> "0040020","cefotaxime allergy","umls","C0571457"
> "0040023","cefaclor allergy","umls","C0571453"
> "7444","obsolete diffuse intraductal papillomatosis","umls","C1377912"
> "7444","obsolete diffuse intraductal papillomatosis","mondo","0004226"
> "13159","scrotum squamous cell carcinoma","umls","C0349551"
> "13159","scrotum squamous cell carcinoma","mondo","0001651"
> "10593","idiopathic progressive polyneuropathy","icd9cm","356.4"
> "10593","idiopathic progressive polyneuropathy","umls","C0154756"
> "10593","idiopathic progressive polyneuropathy","mondo","0001073"
> "10590","mild pre-eclampsia","icd9cm","642.40"
> "10590","mild pre-eclampsia","umls","C0156664"
> "10590","mild pre-eclampsia","mondo","0001072"
> "10591","pre-eclampsia","icd10cm","O14"
> "10591","pre-eclampsia","icd10cm","O14.9"
> "10591","pre-eclampsia","icd10cm","O14.90"
> "10591","pre-eclampsia","mesh","D011225"
> "10591","pre-eclampsia","umls","C0032914"
> "10591","pre-eclampsia","mondo","0005081"
> "10595","Charcot-Marie-Tooth disease","icd10cm","G60.0"
> "10595","Charcot-Marie-Tooth disease","icd9cm","356.1"
> "10595","Charcot-Marie-Tooth disease","mesh","D002607"
> "10595","Charcot-Marie-Tooth disease","umls","C0007959"
> "10595","Charcot-Marie-Tooth disease","mondo","0015626"
> "1935","Bardet-Biedl syndrome","icd10cm","Q87.89"
> "1935","Bardet-Biedl syndrome","mesh","D020788"
> "1935","Bardet-Biedl syndrome","umls","C0752166"
> "1935","Bardet-Biedl syndrome","mondo","0015229"
> "10250","louping ill","icd10cm","A84.8"
> "10250","louping ill","icd9cm","063.1"
> "10250","louping ill","mesh","D008146"
> "10250","louping ill","umls","C0024025"
> "10250","louping ill","mondo","0005829"
> "7013","ovarian mucinous cystadenofibroma","umls","C1518725"
> "7013","ovarian mucinous cystadenofibroma","mondo","0004074"
> "9111","cutaneous leishmaniasis","icd10cm","B55.1"
> "9111","cutaneous leishmaniasis","mesh","D016773"
> "9111","cutaneous leishmaniasis","umls","C0023283"
> "9111","cutaneous leishmaniasis","mondo","0005446"
> "9446","cholangitis","icd10cm","K83.0"
> "9446","cholangitis","icd9cm","576.1"
> "9446","cholangitis","mesh","D002761"
> "9446","cholangitis","umls","C0008311"
> "9446","cholangitis","mondo","0004789"
> "9445","cervix squamous papilloma","umls","C1336900"
> "9445","cervix squamous papilloma","mondo","0004788"
> "0070157","hereditary sensory and autonomic neuropathy type 1C","mondo","0013337"
> "0060791","hypomyelinating leukodystrophy 9","icd10cm","E75.2"
> "0060791","hypomyelinating leukodystrophy 9","mondo","0014506"
> "12995","conduct disorder","icd10cm","F91"
> "12995","conduct disorder","icd10cm","F91.9"
> "12995","conduct disorder","icd9cm","312.9"
> "12995","conduct disorder","mesh","D019955"
> "12995","conduct disorder","umls","C0149654"
> "12995","conduct disorder","mondo","0005352"
> "12996","acute dacryocystitis","icd10cm","H04.32"
> "12996","acute dacryocystitis","icd9cm","375.32"
> "12996","acute dacryocystitis","umls","C0155237"
> "12996","acute dacryocystitis","mondo","0001610"
> "0060790","hypomyelinating leukodystrophy 3","icd10cm","E75.2"
> "0060790","hypomyelinating leukodystrophy 3","mondo","0009843"
> "0060793","hypomyelinating leukodystrophy 5","icd10cm","G37.8"
> "0060793","hypomyelinating leukodystrophy 5","mondo","0012514"
> "0060792","hypomyelinating leukodystrophy 11","icd10cm","G11.1"
> "0060792","hypomyelinating leukodystrophy 11","mondo","0014666"
> "0060795","hypomyelinating leukodystrophy 13","mondo","0014813"
> "12286","testicular leukemia","umls","C1336711"
> "12286","testicular leukemia","mondo","0001482"
> "0060066","pyridoxine-responsive sideroblastic anemia","mondo","0008786"
> "12287","Crimean-Congo hemorrhagic fever","icd10cm","A98.0"
> "12287","Crimean-Congo hemorrhagic fever","icd9cm","065.0"
> "12287","Crimean-Congo hemorrhagic fever","mesh","D006479"
> "12287","Crimean-Congo hemorrhagic fever","umls","C0019099"
> "12287","Crimean-Congo hemorrhagic fever","mondo","0020501"
> "0060065","autosomal recessive pyridoxine-refractory sideroblastic anemia 2","mondo","0008785"
> "0060378","orofaciodigital syndrome VIII","mesh","C557820"
> "0060378","orofaciodigital syndrome VIII","umls","C0796101"
> "0060378","orofaciodigital syndrome VIII","mondo","0010336"
> "0060377","orofaciodigital syndrome VII","mesh","C563104"
> "0060377","orofaciodigital syndrome VII","mondo","0012049"
> "0060376","Joubert syndrome with orofaciodigital defect","mesh","C536531"
> "0060376","Joubert syndrome with orofaciodigital defect","umls","C2745997"
> "0060376","Joubert syndrome with orofaciodigital defect","mondo","0010176"
> "0060375","orofaciodigital syndrome V","mesh","C557819"
> "0060375","orofaciodigital syndrome V","umls","C1868118"
> "0060375","orofaciodigital syndrome V","mondo","0008267"
> "0060374","orofaciodigital syndrome IV","mesh","C537133"
> "0060374","orofaciodigital syndrome IV","umls","C0406727"
> "0060374","orofaciodigital syndrome IV","mondo","0009794"
> "0060373","orofaciodigital syndrome III","mesh","C557817"
> "0060373","orofaciodigital syndrome III","umls","C0406726"
> "0060373","orofaciodigital syndrome III","mondo","0009793"
> "0060372","Parkinson's disease 15","mondo","0009830"
> "0060371","Parkinson's disease 8","mondo","0011764"
> "0060370","Parkinson's disease 7","mondo","0011658"
> "12282","femoral vein thrombophlebitis","icd10cm","I80.1"
> "12282","femoral vein thrombophlebitis","icd9cm","451.11"
> "12282","femoral vein thrombophlebitis","umls","C0265066"
> "12282","femoral vein thrombophlebitis","mondo","0001481"
> "450","myotonic disease","icd10cm","G71.1"
> "450","myotonic disease","icd9cm","359.2"
> "450","myotonic disease","mesh","D020967"
> "450","myotonic disease","umls","C0553604"
> "450","myotonic disease","mondo","0016107"
> "452","pleomorphic adenoma","mesh","D008949"
> "452","pleomorphic adenoma","umls","C0026277"
> "452","pleomorphic adenoma","mondo","0008401"
> "1343","urethritis","icd10cm","N34.2"
> "1343","urethritis","icd9cm","597.80"
> "1343","urethritis","mesh","D014526"
> "1343","urethritis","umls","C0041976"
> "1343","urethritis","umls","C0311389"
> "1343","urethritis","mondo","0005297"
> "456","ascariasis","icd10cm","B77"
> "456","ascariasis","icd10cm","B77.9"
> "456","ascariasis","icd9cm","127.0"
> "456","ascariasis","mesh","D001196"
> "456","ascariasis","umls","C0003950"
> "456","ascariasis","mondo","0005654"
> "8118","mature gastric teratoma","umls","C1334635"
> "8118","mature gastric teratoma","mondo","0004467"
> "8119","anal canal Paget's disease","umls","C1332261"
> "8119","anal canal Paget's disease","mondo","0004468"
> "6929","retinal edema","icd10cm","H35.81"
> "6929","retinal edema","icd9cm","362.83"
> "6929","retinal edema","mesh","D010211"
> "6929","retinal edema","umls","C0242420"
> "6929","retinal edema","mondo","0004037"
> "6925","peroneal nerve paralysis","icd10cm","G57.3"
> "6925","peroneal nerve paralysis","mesh","D020427"
> "6925","peroneal nerve paralysis","umls","C0270810"
> "6925","peroneal nerve paralysis","mondo","0006903"
> "8110","periampullary adenocarcinoma","umls","C1335377"
> "8110","periampullary adenocarcinoma","mondo","0004465"
> "8117","neuronitis","umls","C0027881"
> "8117","neuronitis","mondo","0004466"
> "7713","tuberculum sellae meningioma","umls","C1336829"
> "7713","tuberculum sellae meningioma","mondo","0004339"
> "13374","fibrodysplasia ossificans progressiva","icd10cm","M61.1"
> "13374","fibrodysplasia ossificans progressiva","icd10cm","M61.10"
> "13374","fibrodysplasia ossificans progressiva","icd9cm","728.11"
> "13374","fibrodysplasia ossificans progressiva","mesh","D009221"
> "13374","fibrodysplasia ossificans progressiva","umls","C0016037"
> "13374","fibrodysplasia ossificans progressiva","mondo","0007606"
> "7717","colloid carcinoma of the pancreas","umls","C1333081"
> "7717","colloid carcinoma of the pancreas","mondo","0004341"
> "7716","mixed ductal-endocrine carcinoma","umls","C1301048"
> "7716","mixed ductal-endocrine carcinoma","mondo","0004340"
> "13372","alpha 1-antitrypsin deficiency","icd10cm","E88.01"
> "13372","alpha 1-antitrypsin deficiency","icd9cm","273.4"
> "13372","alpha 1-antitrypsin deficiency","mesh","D019896"
> "13372","alpha 1-antitrypsin deficiency","umls","C0221757"
> "13372","alpha 1-antitrypsin deficiency","mondo","0013282"
> "0060119","pharynx cancer","mesh","D010610"
> "0060119","pharynx cancer","umls","C0031347"
> "0060119","pharynx cancer","mondo","0005517"
> "0090139","cortisone reductase deficiency","mesh","C536447"
> "0090139","cortisone reductase deficiency","mondo","0000193"
> "0014667","disease of metabolism","icd10cm","E88.9"
> "0014667","disease of metabolism","icd9cm","277.9"
> "0014667","disease of metabolism","mesh","D008659"
> "0014667","disease of metabolism","umls","C0025517"
> "0014667","disease of metabolism","mondo","0005066"
> "0090136","complex cortical dysplasia with other brain malformations 6","mondo","0014341"
> "4008","fallopian tube transitional cell carcinoma","umls","C1517128"
> "4008","fallopian tube transitional cell carcinoma","mondo","0002833"
> "4000","ovary transitional cell carcinoma","umls","C1335184"
> "4000","ovary transitional cell carcinoma","umls","C1335185"
> "4000","ovary transitional cell carcinoma","umls","C1518237"
> "4000","ovary transitional cell carcinoma","mondo","0006343"
> "4001","ovarian carcinoma","mesh","C538090"
> "4001","ovarian carcinoma","umls","C0677886"
> "4001","ovarian carcinoma","mondo","0005140"
> "4003","Schneiderian carcinoma","umls","C0334270"
> "4003","Schneiderian carcinoma","mondo","0002831"
> "4005","endometrial transitional cell carcinoma","umls","C1516864"
> "4005","endometrial transitional cell carcinoma","mondo","0002832"
> "4006","bladder urothelial carcinoma","umls","C0279680"
> "4006","bladder urothelial carcinoma","mondo","0005611"
> "4007","bladder carcinoma","umls","C0699885"
> "4007","bladder carcinoma","mondo","0004986"
> "3973","thyroid gland medullary carcinoma","mesh","C536914"
> "3973","thyroid gland medullary carcinoma","umls","C0238462"
> "3973","thyroid gland medullary carcinoma","mondo","0015277"
> "3978","extrinsic cardiomyopathy","icd9cm","425.8"
> "3978","extrinsic cardiomyopathy","umls","C0155699"
> "3978","extrinsic cardiomyopathy","mondo","0002824"
> "0080068","Charcot-Marie-Tooth disease type 6","mondo","0019551"
> "0080065","autosomal recessive spinocerebellar ataxia 19","mondo","0014572"
> "3620","central nervous system cancer","icd10cm","C72.9"
> "3620","central nervous system cancer","mesh","D016543"
> "3620","central nervous system cancer","umls","C0085136"
> "3620","central nervous system cancer","umls","C0348374"
> "3620","central nervous system cancer","mondo","0002714"
> "0080067","Charcot-Marie-Tooth disease type 5","mondo","0010877"
> "0080066","autosomal recessive spinocerebellar ataxia 20","mondo","0014601"
> "0080061","autosomal recessive spinocerebellar ataxia 2","mondo","0008943"
> "0080060","autosomal recessive spinocerebellar ataxia 12","mondo","0013687"
> "3627","aortic aneurysm","icd10cm","I71.1"
> "3627","aortic aneurysm","icd10cm","I71.3"
> "3627","aortic aneurysm","icd10cm","I71.5"
> "3627","aortic aneurysm","icd10cm","I71.8"
> "3627","aortic aneurysm","icd10cm","I71.9"
> "3627","aortic aneurysm","icd9cm","441.1"
> "3627","aortic aneurysm","icd9cm","441.3"
> "3627","aortic aneurysm","icd9cm","441.5"
> "3627","aortic aneurysm","icd9cm","441.6"
> "3627","aortic aneurysm","mesh","D001014"
> "3627","aortic aneurysm","mesh","D001019"
> "3627","aortic aneurysm","umls","C0003486"
> "3627","aortic aneurysm","umls","C0265010"
> "3627","aortic aneurysm","umls","C0265012"
> "3627","aortic aneurysm","umls","C0741160"
> "3627","aortic aneurysm","umls","C1305122"
> "3627","aortic aneurysm","mondo","0005160"
> "0080062","autosomal recessive spinocerebellar ataxia 13","mondo","0013905"
> "13996","small intestine lymphoma","umls","C0278805"
> "13996","small intestine lymphoma","mondo","0001852"
> "13999","contact blepharoconjunctivitis","icd10cm","H10.53"
> "13999","contact blepharoconjunctivitis","icd9cm","372.22"
> "13999","contact blepharoconjunctivitis","umls","C0155150"
> "13999","contact blepharoconjunctivitis","mondo","0001853"
> "0060185","Clostridium difficile colitis","icd10cm","A04.7"
> "0060185","Clostridium difficile colitis","mesh","D004761"
> "0060185","Clostridium difficile colitis","umls","C0014358"
> "0060185","Clostridium difficile colitis","umls","C0085819"
> "0060185","Clostridium difficile colitis","umls","C1257843"
> "0060185","Clostridium difficile colitis","umls","C1257844"
> "0060185","Clostridium difficile colitis","umls","C1257845"
> "0060185","Clostridium difficile colitis","mondo","0000705"
> "4479","pseudohypoaldosteronism","mesh","D011546"
> "4479","pseudohypoaldosteronism","umls","C0033805"
> "4479","pseudohypoaldosteronism","mondo","0018638"
> "13369","tinea manuum","icd10cm","B35.2"
> "13369","tinea manuum","icd9cm","110.2"
> "13369","tinea manuum","umls","C0153246"
> "13369","tinea manuum","mondo","0001699"
> "14225","acute frontal sinusitis","icd10cm","J01.1"
> "14225","acute frontal sinusitis","icd10cm","J01.10"
> "14225","acute frontal sinusitis","icd9cm","461.1"
> "14225","acute frontal sinusitis","umls","C0155805"
> "14225","acute frontal sinusitis","mondo","0001912"
> "4471","chromophobe renal cell carcinoma","mesh","D002292"
> "4471","chromophobe renal cell carcinoma","umls","C1266042"
> "4471","chromophobe renal cell carcinoma","mondo","0017885"
> "4473","sarcomatoid renal cell carcinoma","mesh","D002292"
> "4473","sarcomatoid renal cell carcinoma","umls","C1266043"
> "4473","sarcomatoid renal cell carcinoma","mondo","0003012"
> "4472","mucinous tubular and spindle renal cell carcinoma","umls","C1513719"
> "4472","mucinous tubular and spindle renal cell carcinoma","mondo","0003011"
> "13364","obsolete chronobiology disease","mesh","D021081"
> "13364","obsolete chronobiology disease","umls","C0236811"
> "13365","reading disorder","icd9cm","315.09"
> "13365","reading disorder","umls","C0154631"
> "13365","reading disorder","mondo","0001697"
> "13366","Stiff-Person syndrome","icd10cm","G25.82"
> "13366","Stiff-Person syndrome","icd9cm","333.91"
> "13366","Stiff-Person syndrome","mesh","D016750"
> "13366","Stiff-Person syndrome","umls","C0085292"
> "13366","Stiff-Person syndrome","mondo","0008491"
> "0090143","brachyolmia-amelogenesis imperfecta syndrome","icd10cm","Q76.3"
> "0090143","brachyolmia-amelogenesis imperfecta syndrome","mondo","0011018"
> "0090142","cystathioninuria","icd10cm","E72.19"
> "0090142","cystathioninuria","mesh","C535408"
> "0090142","cystathioninuria","umls","C0220993"
> "0090142","cystathioninuria","umls","C0268616"
> "0090142","cystathioninuria","mondo","0009058"
> "0090141","cortisone reductase deficiency 1","mondo","0011503"
> "0090140","cortisone reductase deficiency 2","mondo","0013842"
> "0090145","dopamine beta-hydroxylase deficiency","mesh","C535600"
> "0090145","dopamine beta-hydroxylase deficiency","umls","C0342687"
> "0090145","dopamine beta-hydroxylase deficiency","mondo","0009123"
> "0090144","Donnai-Barrow syndrome","mesh","C536390"
> "0090144","Donnai-Barrow syndrome","umls","C1857277"
> "0090144","Donnai-Barrow syndrome","mondo","0009104"
> "1025","tuberculoid leprosy","icd10cm","A30.1"
> "1025","tuberculoid leprosy","icd9cm","030.1"
> "1025","tuberculoid leprosy","mesh","D015441"
> "1025","tuberculoid leprosy","umls","C0023351"
> "1025","tuberculoid leprosy","mondo","0005126"
> "2460","anterior dislocation of lens","icd10cm","H27.12"
> "2460","anterior dislocation of lens","icd9cm","379.33"
> "2460","anterior dislocation of lens","umls","C0155372"
> "2460","anterior dislocation of lens","mondo","0002310"
> "2462","retinal vascular disease","umls","C0154833"
> "2462","retinal vascular disease","mondo","0002311"
> "1024","leprosy","icd10cm","A30"
> "1024","leprosy","icd10cm","A30.9"
> "1024","leprosy","icd9cm","030"
> "1024","leprosy","icd9cm","030.9"
> "1024","leprosy","mesh","D007918"
> "1024","leprosy","umls","C0023343"
> "1024","leprosy","mondo","0005124"
> "2468","psychotic disorder","icd9cm","298.8"
> "2468","psychotic disorder","umls","C0029516"
> "2468","psychotic disorder","mondo","0005485"
> "0110610","primary ciliary dyskinesia 34","mondo","0014909"
> "0110611","primary ciliary dyskinesia 27","icd10cm","Q34.8"
> "0110611","primary ciliary dyskinesia 27","mondo","0014215"
> "0110612","primary ciliary dyskinesia 10","icd10cm","Q34.8"
> "0110612","primary ciliary dyskinesia 10","mondo","0012918"
> "0110613","primary ciliary dyskinesia 16","icd10cm","Q34.8"
> "0110613","primary ciliary dyskinesia 16","mondo","0013525"
> "0110614","primary ciliary dyskinesia 4","icd10cm","Q34.8"
> "0110614","primary ciliary dyskinesia 4","mondo","0012087"
> "0110615","primary ciliary dyskinesia 25","icd10cm","Q34.8"
> "0110615","primary ciliary dyskinesia 25","mondo","0014203"
> "0110616","primary ciliary dyskinesia 8","icd10cm","Q34.8"
> "0110616","primary ciliary dyskinesia 8","mondo","0012844"
> "0110617","primary ciliary dyskinesia 5","icd10cm","Q34.8"
> "0110617","primary ciliary dyskinesia 5","mondo","0012088"
> "0110618","primary ciliary dyskinesia 13","icd10cm","Q34.8"
> "0110618","primary ciliary dyskinesia 13","mondo","0013174"
> "0110619","primary ciliary dyskinesia 33","icd10cm","Q34.8"
> "0110619","primary ciliary dyskinesia 33","mondo","0014750"
> "1022","pinta disease","icd10cm","A67"
> "1022","pinta disease","icd10cm","A67.0"
> "1022","pinta disease","icd10cm","A67.1"
> "1022","pinta disease","icd10cm","A67.2"
> "1022","pinta disease","icd10cm","A67.3"
> "1022","pinta disease","icd10cm","A67.9"
> "1022","pinta disease","icd9cm","103"
> "1022","pinta disease","icd9cm","103.0"
> "1022","pinta disease","icd9cm","103.1"
> "1022","pinta disease","icd9cm","103.2"
> "1022","pinta disease","icd9cm","103.3"
> "1022","pinta disease","icd9cm","103.9"
> "1022","pinta disease","mesh","D010874"
> "1022","pinta disease","umls","C0031946"
> "1022","pinta disease","umls","C0153241"
> "1022","pinta disease","umls","C0153242"
> "1022","pinta disease","umls","C0153243"
> "1022","pinta disease","umls","C0153244"
> "1022","pinta disease","mondo","0000979"
> "6312","clivus chordoma","umls","C1333071"
> "6312","clivus chordoma","mondo","0003849"
> "6313","clivus chondroid chordoma","umls","C1333072"
> "6313","clivus chondroid chordoma","mondo","0003850"
> "12140","Chagas disease","kegg","05142"
> "12140","Chagas disease","icd9cm","086.2"
> "12140","Chagas disease","mesh","D014355"
> "12140","Chagas disease","umls","C0007932"
> "12140","Chagas disease","mondo","0001444"
> "6316","Bartholin's gland adenocarcinoma","umls","C0238016"
> "6316","Bartholin's gland adenocarcinoma","mondo","0003853"
> "6314","ovarian fetiform teratoma","umls","C1518715"
> "6314","ovarian fetiform teratoma","mondo","0003851"
> "6315","ovarian solid teratoma","umls","C1335181"
> "6315","ovarian solid teratoma","mondo","0003852"
> "12148","alveolar echinococcosis","icd10cm","B67.6"
> "12148","alveolar echinococcosis","icd10cm","B67.7"
> "12148","alveolar echinococcosis","icd9cm","122.7"
> "12148","alveolar echinococcosis","mesh","C536591"
> "12148","alveolar echinococcosis","umls","C0152069"
> "12148","alveolar echinococcosis","mondo","0017282"
> "0111527","spinal muscular atrophy with progressive myoclonic epilepsy","mesh","C537563"
> "0111527","spinal muscular atrophy with progressive myoclonic epilepsy","umls","C1834569"
> "0111526","Mullerian aplasia and hyperandrogenism","mesh","C567186"
> "0111526","Mullerian aplasia and hyperandrogenism","umls","C2675014"
> "0111529","familial multiple nevi flammei","mesh","C535816"
> "0111529","familial multiple nevi flammei","umls","C2931029"
> "1029","familial periodic paralysis","icd10cm","G72.3"
> "1029","familial periodic paralysis","mesh","D010245"
> "1029","familial periodic paralysis","umls","C0030443"
> "1029","familial periodic paralysis","mondo","0000995"
> "10439","Mooren's ulcer","icd10cm","H16.05"
> "10439","Mooren's ulcer","icd9cm","370.07"
> "10439","Mooren's ulcer","umls","C0155072"
> "10439","Mooren's ulcer","mondo","0001032"
> "9650","pathologic nystagmus","icd10cm","H55.0"
> "9650","pathologic nystagmus","icd10cm","H55.00"
> "9650","pathologic nystagmus","icd9cm","379.50"
> "9650","pathologic nystagmus","mesh","D009759"
> "9650","pathologic nystagmus","umls","C0028738"
> "9650","pathologic nystagmus","mondo","0004843"
> "9651","systolic heart failure","icd10cm","I50.20"
> "9651","systolic heart failure","icd9cm","428.2"
> "9651","systolic heart failure","icd9cm","428.20"
> "9651","systolic heart failure","mesh","D054143"
> "9651","systolic heart failure","umls","C1135191"
> "9651","systolic heart failure","mondo","0006993"
> "9655","oral mucosa leukoplakia","icd10cm","K13.2"
> "9655","oral mucosa leukoplakia","icd10cm","K13.21"
> "9655","oral mucosa leukoplakia","icd9cm","528.6"
> "9655","oral mucosa leukoplakia","umls","C1112530"
> "9655","oral mucosa leukoplakia","mondo","0004844"
> "10123","pigmentation disease","icd9cm","709.09"
> "10123","pigmentation disease","umls","C0375489"
> "10123","pigmentation disease","mondo","0019288"
> "9305","splenic tuberculosis","icd10cm","A18.85"
> "9305","splenic tuberculosis","icd9cm","017.7"
> "9305","splenic tuberculosis","mesh","D014400"
> "9305","splenic tuberculosis","umls","C0041331"
> "9305","splenic tuberculosis","mondo","0005967"
> "9306","mechanical strabismus","icd10cm","H50.6"
> "9306","mechanical strabismus","icd10cm","H50.60"
> "9306","mechanical strabismus","icd9cm","378.6"
> "9306","mechanical strabismus","icd9cm","378.60"
> "9306","mechanical strabismus","mesh","D013285"
> "9306","mechanical strabismus","umls","C0152223"
> "9306","mechanical strabismus","mondo","0004753"
> "9307","rectal prolapse","icd10cm","K62.3"
> "9307","rectal prolapse","icd9cm","569.1"
> "9307","rectal prolapse","mesh","D012005"
> "9307","rectal prolapse","umls","C0034888"
> "9307","rectal prolapse","mondo","0004754"
> "9300","neurofibroma of the heart","umls","C1096349"
> "9300","neurofibroma of the heart","mondo","0004752"
> "10126","keratoconus","icd10cm","H18.6"
> "10126","keratoconus","icd10cm","H18.60"
> "10126","keratoconus","icd9cm","371.6"
> "10126","keratoconus","icd9cm","371.60"
> "10126","keratoconus","mesh","D007640"
> "10126","keratoconus","umls","C0022578"
> "10126","keratoconus","mondo","0015486"
> "10125","acute hydrops keratoconus","icd9cm","371.62"
> "10125","acute hydrops keratoconus","umls","C0339286"
> "10125","acute hydrops keratoconus","mondo","0000943"
> "10124","corneal disease","icd10cm","H18.9"
> "10124","corneal disease","icd9cm","371.9"
> "10124","corneal disease","mesh","D003316"
> "10124","corneal disease","umls","C0010034"
> "10124","corneal disease","mondo","0000942"
> "0050587","trichotillomania","mesh","D014256"
> "0050587","trichotillomania","mondo","0013189"
> "0050585","congenital generalized lipodystrophy","mondo","0006536"
> "0050581","brachydactyly","mondo","0021004"
> "0050580","hereditary lymphedema","icd9cm","757.0"
> "0050580","hereditary lymphedema","umls","C1313885"
> "0050580","hereditary lymphedema","mondo","0019313"
> "0050589","inflammatory bowel disease","kegg","05321"
> "0050589","inflammatory bowel disease","mesh","D015212"
> "0050589","inflammatory bowel disease","umls","C0021390"
> "0050589","inflammatory bowel disease","mondo","0005265"
> "0050588","muscular dystrophy-dystroglycanopathy","icd10cm","G71.2"
> "0050588","muscular dystrophy-dystroglycanopathy","mondo","0018276"
> "8969","tonsillar fossa cancer","icd10cm","C09.0"
> "8969","tonsillar fossa cancer","icd9cm","146.1"
> "8969","tonsillar fossa cancer","umls","C0153384"
> "8969","tonsillar fossa cancer","mondo","0004690"
> "0110603","primary ciliary dyskinesia 32","icd10cm","Q34.8"
> "0110603","primary ciliary dyskinesia 32","mondo","0014657"
> "0110602","primary ciliary dyskinesia 11","icd10cm","Q34.8"
> "0110602","primary ciliary dyskinesia 11","mondo","0012978"
> "1647","female breast upper-inner quadrant cancer","icd9cm","174.2"
> "1647","female breast upper-inner quadrant cancer","umls","C0153550"
> "1647","female breast upper-inner quadrant cancer","mondo","0002067"
> "1641","benign breast adenomyoepithelioma","umls","C1332477"
> "1641","benign breast adenomyoepithelioma","mondo","0002065"
> "1642","breast adenomyoepithelioma","umls","C1334564"
> "1642","breast adenomyoepithelioma","umls","C1510795"
> "1642","breast adenomyoepithelioma","mondo","0002066"
> "1649","female breast lower-inner quadrant cancer","icd10cm","C50.31"
> "1649","female breast lower-inner quadrant cancer","icd9cm","174.3"
> "1649","female breast lower-inner quadrant cancer","umls","C0153551"
> "1649","female breast lower-inner quadrant cancer","mondo","0002068"
> "0110609","primary ciliary dyskinesia 23","icd10cm","Q34.8"
> "0110609","primary ciliary dyskinesia 23","mondo","0014193"
> "0110970","brachydactyly type C","mesh","C537093"
> "0110970","brachydactyly type C","umls","C1300268"
> "0110970","brachydactyly type C","umls","C1862103"
> "0110970","brachydactyly type C","mondo","0007221"
> "0110608","primary ciliary dyskinesia 19","icd10cm","Q34.8"
> "0110608","primary ciliary dyskinesia 19","mondo","0013979"
> "573","nerve compression syndrome","mesh","D009408"
> "573","nerve compression syndrome","umls","C0027743"
> "573","nerve compression syndrome","umls","C1510429"
> "573","nerve compression syndrome","mondo","0003615"
> "572","mononeuritis of upper limb and mononeuritis multiplex","icd9cm","354"
> "572","mononeuritis of upper limb and mononeuritis multiplex","umls","C0154741"
> "572","mononeuritis of upper limb and mononeuritis multiplex","mondo","0003607"
> "571","median neuropathy","icd10cm","G56.1"
> "571","median neuropathy","icd10cm","G56.10"
> "571","median neuropathy","icd9cm","354.1"
> "571","median neuropathy","mesh","D020423"
> "571","median neuropathy","umls","C0154742"
> "571","median neuropathy","mondo","0003598"
> "576","proteinuria","icd10cm","R80"
> "576","proteinuria","icd10cm","R80.9"
> "576","proteinuria","icd9cm","791.0"
> "576","proteinuria","mesh","D011507"
> "576","proteinuria","umls","C0033687"
> "576","proteinuria","mondo","0003634"
> "574","peripheral nervous system disease","icd10cm","G64"
> "574","peripheral nervous system disease","icd9cm","350-359.99"
> "574","peripheral nervous system disease","mesh","D010523"
> "574","peripheral nervous system disease","umls","C0031117"
> "574","peripheral nervous system disease","umls","C1335029"
> "574","peripheral nervous system disease","mondo","0003620"
> "0050976","spinocerebellar ataxia type 27","mondo","0012247"
> "0050977","spinocerebellar ataxia type 28","mondo","0012450"
> "0050974","spinocerebellar ataxia type 25","mesh","C537202"
> "0050974","spinocerebellar ataxia type 25","mondo","0012103"
> "0050975","spinocerebellar ataxia type 26","mesh","C537203"
> "0050975","spinocerebellar ataxia type 26","mondo","0012246"
> "0050972","spinocerebellar ataxia type 21","mondo","0011833"
> "0050973","spinocerebellar ataxia type 23","mondo","0012449"
> "0050970","spinocerebellar ataxia type 19/22","mondo","0011819"
> "0050971","spinocerebellar ataxia type 20","mondo","0012098"
> "2800","acute interstitial pneumonia","icd10cm","J84.114"
> "2800","acute interstitial pneumonia","icd9cm","516.33"
> "2800","acute interstitial pneumonia","umls","C1279945"
> "2800","acute interstitial pneumonia","mondo","0019203"
> "2801","nonspecific interstitial pneumonia","umls","C1290344"
> "2801","nonspecific interstitial pneumonia","mondo","0019622"
> "0050978","spinocerebellar ataxia type 29","mondo","0007298"
> "0050979","spinocerebellar ataxia type 30","mondo","0013241"
> "5432","bladder papillary transitional cell neoplasm","umls","C1511197"
> "5432","bladder papillary transitional cell neoplasm","mondo","0003442"
> "5433","urinary tract papillary transitional cell benign neoplasm","umls","C1334282"
> "5433","urinary tract papillary transitional cell benign neoplasm","umls","C1335329"
> "5433","urinary tract papillary transitional cell benign neoplasm","mondo","0003443"
> "3368","Ewing sarcoma of bone","umls","C0585474"
> "3368","Ewing sarcoma of bone","umls","C1333481"
> "3368","Ewing sarcoma of bone","umls","C1334406"
> "3368","Ewing sarcoma of bone","mondo","0002625"
> "5437","intrahepatic bile duct adenoma","umls","C1331535"
> "5437","intrahepatic bile duct adenoma","mondo","0003444"
> "5434","scrapie","mesh","D012608"
> "5434","scrapie","umls","C0036457"
> "5434","scrapie","mondo","0006961"
> "5435","variant Creutzfeldt-Jakob disease","mesh","D016643"
> "5435","variant Creutzfeldt-Jakob disease","umls","C0085209"
> "5435","variant Creutzfeldt-Jakob disease","mondo","0007012"
> "1428","endocrine pancreas disease","icd10cm","E16"
> "1428","endocrine pancreas disease","icd9cm","251"
> "1428","endocrine pancreas disease","umls","C0154189"
> "1428","endocrine pancreas disease","mondo","0001933"
> "5438","extrahepatic bile duct adenoma","umls","C1331534"
> "5438","extrahepatic bile duct adenoma","mondo","0003445"
> "5439","papillary hidradenoma","mesh","D000074009"
> "5439","papillary hidradenoma","umls","C0334348"
> "5439","papillary hidradenoma","mondo","0003446"
> "3360","multifocal osteogenic sarcoma","umls","C1334820"
> "3360","multifocal osteogenic sarcoma","mondo","0002622"
> "3361","pediatric osteosarcoma","umls","C1332986"
> "3361","pediatric osteosarcoma","mondo","0002623"
> "3362","coronary aneurysm","icd10cm","I25.41"
> "3362","coronary aneurysm","icd9cm","414.11"
> "3362","coronary aneurysm","mesh","D003323"
> "3362","coronary aneurysm","umls","C0010051"
> "3362","coronary aneurysm","mondo","0006714"
> "14735","hereditary angioedema","mesh","D054179"
> "14735","hereditary angioedema","umls","C0019243"
> "14735","hereditary angioedema","mondo","0019623"
> "2018","hyperinsulinism","icd10cm","E16.1"
> "2018","hyperinsulinism","mesh","D006946"
> "2018","hyperinsulinism","umls","C0020459"
> "2018","hyperinsulinism","mondo","0002177"
> "0060584","Noonan syndrome 6","icd10cm","Q87.1"
> "0060584","Noonan syndrome 6","mondo","0013186"
> "0060585","Noonan syndrome 7","icd10cm","Q87.1"
> "0060585","Noonan syndrome 7","mondo","0013379"
> "0060586","Noonan syndrome 8","icd10cm","Q87.1"
> "0060586","Noonan syndrome 8","mondo","0014143"
> "4270","encephalitozoonosis","mesh","D016890"
> "4270","encephalitozoonosis","umls","C0085412"
> "4270","encephalitozoonosis","mondo","0005743"
> "0060580","Noonan syndrome 2","icd10cm","Q87.1"
> "0060580","Noonan syndrome 2","mondo","0011531"
> "0060581","Noonan syndrome 3","icd10cm","Q87.1"
> "0060581","Noonan syndrome 3","mondo","0012371"
> "0060582","Noonan syndrome 4","icd10cm","Q87.1"
> "0060582","Noonan syndrome 4","mondo","0012547"
> "0060583","Noonan syndrome 5","icd10cm","Q87.1"
> "0060583","Noonan syndrome 5","mondo","0012690"
> "4279","infundibulocystic basal cell carcinoma","mondo","0011465"
> "4278","scrotum basal cell carcinoma","umls","C1335934"
> "4278","scrotum basal cell carcinoma","mondo","0002936"
> "0060588","Noonan syndrome 10","icd10cm","Q87.1"
> "0060588","Noonan syndrome 10","mondo","0014693"
> "0060589","Yunis-Varon syndrome","mesh","C536719"
> "0060589","Yunis-Varon syndrome","umls","C1857663"
> "0060589","Yunis-Varon syndrome","mondo","0008995"
> "0111266","geroderma osteodysplasticum","mesh","C537799"
> "0111266","geroderma osteodysplasticum","umls","C0432255"
> "5557","testicular germ cell cancer","mesh","C563236"
> "5557","testicular germ cell cancer","umls","C1336708"
> "5557","testicular germ cell cancer","mondo","0010108"
> "5556","testicular malignant germ cell cancer","umls","C0855197"
> "5556","testicular malignant germ cell cancer","mondo","0003510"
> "5551","choriocarcinoma of the testis","umls","C0238449"
> "5551","choriocarcinoma of the testis","mondo","0003508"
> "5550","choriocarcinoma of ovary","umls","C0346181"
> "5550","choriocarcinoma of ovary","mondo","0003507"
> "5553","pineal region choriocarcinoma","umls","C1335414"
> "5553","pineal region choriocarcinoma","mondo","0003509"
> "5559","mediastinal cancer","icd10cm","C38.3"
> "5559","mediastinal cancer","icd9cm","164.9"
> "5559","mediastinal cancer","mesh","D008479"
> "5559","mediastinal cancer","umls","C0025063"
> "5559","mediastinal cancer","umls","C0153504"
> "5559","mediastinal cancer","mondo","0005843"
> "13482","Proteus syndrome","mesh","D016715"
> "13482","Proteus syndrome","umls","C0085261"
> "13482","Proteus syndrome","mondo","0008318"
> "0111263","combined malonic and methylmalonic acidemia","umls","C3280314"
> "0111260","phosphoribosylpyrophosphate synthetase superactivity","umls","C1970827"
> "8580","malignant histiocytosis","icd10cm","C96.A"
> "8580","malignant histiocytosis","icd9cm","202.3"
> "8580","malignant histiocytosis","mesh","D054747"
> "8580","malignant histiocytosis","umls","C0019623"
> "8580","malignant histiocytosis","mondo","0004612"
> "0111261","fumarase deficiency","mesh","C538191"
> "0111261","fumarase deficiency","umls","C0342770"
> "0111261","fumarase deficiency","umls","C2936826"
> "8584","Burkitt lymphoma","icd10cm","C83.7"
> "8584","Burkitt lymphoma","icd10cm","C83.70"
> "8584","Burkitt lymphoma","icd9cm","200.2"
> "8584","Burkitt lymphoma","mesh","D002051"
> "8584","Burkitt lymphoma","umls","C0006413"
> "8584","Burkitt lymphoma","mondo","0007243"
> "0060638","neonatal diabetes mellitus with congenital hypothyroidism","mondo","0012436"
> "0060639","permanent neonatal diabetes mellitus","mondo","0011643"
> "5884","benign intermediate mesothelioma","umls","C1337012"
> "5884","benign intermediate mesothelioma","mondo","0003688"
> "6554","ovarian clear cell malignant adenofibroma","mondo","0003922"
> "6552","gastric small cell carcinoma","umls","C1333788"
> "6552","gastric small cell carcinoma","mondo","0006229"
> "6553","posterior foramen magnum meningioma","umls","C1335449"
> "6553","posterior foramen magnum meningioma","mondo","0003921"
> "6559","ethmoid sinus Schneiderian papilloma","umls","C1333476"
> "6559","ethmoid sinus Schneiderian papilloma","mondo","0003923"
> "14559","anaerobic meningitis","icd9cm","320.81"
> "14559","anaerobic meningitis","umls","C0375197"
> "14559","anaerobic meningitis","mondo","0002000"
> "9667","placental abruption","icd10cm","O20.0"
> "9667","placental abruption","icd9cm","640.0"
> "9667","placental abruption","icd9cm","640.03"
> "9667","placental abruption","mesh","D000033"
> "9667","placental abruption","mesh","D000037"
> "9667","placental abruption","umls","C0000821"
> "9667","placental abruption","mondo","0004846"
> "7505","small intestine benign neoplasm","umls","C0345832"
> "7505","small intestine benign neoplasm","mondo","0004251"
> "7506","small intestinal L-cell glucagon-like peptide producing tumor","umls","C3274143"
> "7506","small intestinal L-cell glucagon-like peptide producing tumor","mondo","0004252"
> "9884","muscular dystrophy","icd10cm","G71.0"
> "9884","muscular dystrophy","icd9cm","359.1"
> "9884","muscular dystrophy","mesh","D009136"
> "9884","muscular dystrophy","umls","C0026850"
> "9884","muscular dystrophy","mondo","0020121"
> "9883","Becker muscular dystrophy","umls","C0699741"
> "9883","Becker muscular dystrophy","mondo","0010311"
> "7501","pediatric infratentorial ependymoma","umls","C0278599"
> "7501","pediatric infratentorial ependymoma","mondo","0004248"
> "7502","pediatric supratentorial ependymoma","umls","C0278650"
> "7502","pediatric supratentorial ependymoma","mondo","0004249"
> "9880","cardiovascular syphilis","icd9cm","093.8"
> "9880","cardiovascular syphilis","icd9cm","093.89"
> "9880","cardiovascular syphilis","umls","C0029751"
> "9880","cardiovascular syphilis","mondo","0004911"
> "9888","alternating esotropia","icd10cm","H50.05"
> "9888","alternating esotropia","icd9cm","378.05"
> "9888","alternating esotropia","umls","C0152205"
> "9888","alternating esotropia","mondo","0004913"
> "14557","primary pulmonary hypertension","icd10cm","I27.0"
> "14557","primary pulmonary hypertension","icd9cm","416.0"
> "14557","primary pulmonary hypertension","umls","C0152171"
> "14557","primary pulmonary hypertension","mondo","0001999"
> "12424","thyrocalcitonin secretion disease","icd9cm","246.0"
> "12424","thyrocalcitonin secretion disease","umls","C0701822"
> "12424","thyrocalcitonin secretion disease","mondo","0001525"
> "6126","anal canal carcinoma","mesh","C563020"
> "6126","anal canal carcinoma","umls","C0563211"
> "6126","anal canal carcinoma","mondo","0007108"
> "14555","Foster-Kennedy syndrome","icd10cm","H47.14"
> "14555","Foster-Kennedy syndrome","icd9cm","377.04"
> "14555","Foster-Kennedy syndrome","mesh","D009901"
> "14555","Foster-Kennedy syndrome","umls","C0152112"
> "14555","Foster-Kennedy syndrome","mondo","0001998"
> "6128","gliomatosis cerebri","mesh","D018302"
> "6128","gliomatosis cerebri","umls","C0334576"
> "6128","gliomatosis cerebri","mondo","0016683"
> "4848","cerebellar astrocytoma","umls","C0740480"
> "4848","cerebellar astrocytoma","mondo","0003165"
> "10440","mycotic corneal ulcer","icd10cm","H16.06"
> "10440","mycotic corneal ulcer","icd9cm","370.05"
> "10440","mycotic corneal ulcer","umls","C0155071"
> "10440","mycotic corneal ulcer","mondo","0001033"
> "10441","marginal corneal ulcer","icd10cm","H16.04"
> "10441","marginal corneal ulcer","icd9cm","370.01"
> "10441","marginal corneal ulcer","umls","C0155067"
> "10441","marginal corneal ulcer","mondo","0001034"
> "10442","hypopyon ulcer","icd10cm","H16.03"
> "10442","hypopyon ulcer","icd9cm","370.04"
> "10442","hypopyon ulcer","umls","C0155070"
> "10442","hypopyon ulcer","mondo","0001035"
> "10952","nephritis","icd10cm","N05"
> "10952","nephritis","icd10cm","N08"
> "10952","nephritis","mesh","D009393"
> "10952","nephritis","umls","C0027697"
> "10952","nephritis","mondo","0001166"
> "0040022","amodiaquine allergy","umls","C0571303"
> "13327","anatomical narrow angle borderline glaucoma","icd9cm","365.02"
> "13327","anatomical narrow angle borderline glaucoma","umls","C0154941"
> "13327","anatomical narrow angle borderline glaucoma","mondo","0001686"
> "10955","strongyloidiasis","icd10cm","B78"
> "10955","strongyloidiasis","icd10cm","B78.9"
> "10955","strongyloidiasis","icd9cm","127.2"
> "10955","strongyloidiasis","mesh","D013322"
> "10955","strongyloidiasis","umls","C0038463"
> "10955","strongyloidiasis","mondo","0005974"
> "0050778","Meckel syndrome","icd9cm","753.1"
> "0050778","Meckel syndrome","icd9cm","753.10"
> "0050778","Meckel syndrome","umls","C0311245"
> "0050778","Meckel syndrome","mondo","0018921"
> "0050779","hydrolethalus syndrome","icd10cm","Q87.8"
> "0050779","hydrolethalus syndrome","mesh","C536079"
> "0050779","hydrolethalus syndrome","mondo","0006037"
> "0050774","rapadilino syndrome","mondo","0009955"
> "0050775","schneckenbecken dysplasia","mesh","C536637"
> "0050775","schneckenbecken dysplasia","mondo","0010013"
> "0050776","non-syndromic X-linked intellectual disability","mondo","0019181"
> "0050777","Joubert syndrome","icd10cm","Q04.3"
> "0050777","Joubert syndrome","mondo","0018772"
> "0050770","polycystic liver disease","mondo","0000447"
> "0050771","pheochromocytoma","mesh","D010673"
> "0050771","pheochromocytoma","mondo","0008233"
> "0050772","spastic ataxia 1","mondo","0007164"
> "0050773","paraganglioma","mesh","D010235"
> "0050773","paraganglioma","umls","C0030421"
> "0050773","paraganglioma","mondo","0000448"
> "13521","tetanus neonatorum","icd10cm","A33"
> "13521","tetanus neonatorum","icd9cm","771.3"
> "13521","tetanus neonatorum","umls","C0343312"
> "13521","tetanus neonatorum","mondo","0001737"
> "0111068","congenital bile acid synthesis defect 4","mesh","C535444"
> "0111068","congenital bile acid synthesis defect 4","umls","C1858328"
> "0111068","congenital bile acid synthesis defect 4","mondo","0008967"
> "0111069","congenital bile acid synthesis defect 2","mesh","C535443"
> "0111069","congenital bile acid synthesis defect 2","umls","C1856127"
> "0111069","congenital bile acid synthesis defect 2","mondo","0009339"
> "0111064","distal spinal muscular atrophy 1","icd10cm","G12.2"
> "0111064","distal spinal muscular atrophy 1","mondo","0011436"
> "2256","osteochondrodysplasia","icd10cm","Q78.9"
> "2256","osteochondrodysplasia","icd9cm","756.4"
> "2256","osteochondrodysplasia","mesh","D010009"
> "2256","osteochondrodysplasia","umls","C0008449"
> "2256","osteochondrodysplasia","umls","C0029422"
> "2256","osteochondrodysplasia","mondo","0005516"
> "0111066","congenital bile acid synthesis defect 5","mondo","0014564"
> "0111067","congenital bile acid synthesis defect 6","mondo","0015015"
> "2253","cervix disease","mesh","D002577"
> "2253","cervix disease","umls","C0007867"
> "2253","cervix disease","mondo","0002256"
> "0111061","familial hypobetalipoproteinemia 2","mondo","0011505"
> "0111062","familial hypobetalipoproteinemia 1","mondo","0014252"
> "0111063","hyperphosphatemic familial tumoral calcinosis","icd10cm","M11.2"
> "0111063","hyperphosphatemic familial tumoral calcinosis","mondo","0008897"
> "0050118","La Crosse encephalitis","icd10cm","A83.5"
> "0050118","La Crosse encephalitis","icd9cm","062.5"
> "0050118","La Crosse encephalitis","mesh","D004670"
> "0050118","La Crosse encephalitis","umls","C0014053"
> "0050118","La Crosse encephalitis","mondo","0019378"
> "0110812","hereditary spastic paraplegia 61","icd10cm","G11.4"
> "0110812","hereditary spastic paraplegia 61","mondo","0014304"
> "0080307","myofibrillar myopathy","mesh","C580316"
> "0080307","myofibrillar myopathy","mondo","0018943"
> "0080301","atypical hemolytic-uremic syndrome","mondo","0016244"
> "0080302","mixed sleep apnea","mesh","D012891"
> "0080302","mixed sleep apnea","umls","C0338495"
> "0080302","mixed sleep apnea","mondo","0024358"
> "0110813","hereditary spastic paraplegia 62","icd10cm","G11.4"
> "0110813","hereditary spastic paraplegia 62","mondo","0014302"
> "0080308","myofibrillar myopathy 8","mondo","0014993"
> "0080309","fatal infantile hypertonic myofibrillar myopathy","mondo","0013472"
> "0050117","disease by infectious agent","icd9cm","079.0"
> "0050117","disease by infectious agent","umls","C0001485"
> "0050117","disease by infectious agent","mondo","0005550"
> "2785","Dandy-Walker syndrome","icd10cm","Q03.1"
> "2785","Dandy-Walker syndrome","mesh","D003616"
> "2785","Dandy-Walker syndrome","umls","C0010964"
> "2785","Dandy-Walker syndrome","mondo","0009072"
> "2784","lung sarcoma","umls","C0598790"
> "2784","lung sarcoma","mondo","0002426"
> "2786","cerebellar disease","mesh","D002526"
> "2786","cerebellar disease","umls","C0007760"
> "2786","cerebellar disease","mondo","0002427"
> "2781","rectosigmoid cancer","umls","C1327709"
> "2781","rectosigmoid cancer","mondo","0002424"
> "2780","rectosigmoid junction neoplasm","umls","C0345873"
> "2780","rectosigmoid junction neoplasm","mondo","0002423"
> "2782","rectosigmoid junction cancer","icd10cm","C19"
> "2782","rectosigmoid junction cancer","icd9cm","154.0"
> "2782","rectosigmoid junction cancer","umls","C0153443"
> "2782","rectosigmoid junction cancer","mondo","0002425"
> "0110816","hereditary spastic paraplegia 7","icd10cm","G11.4"
> "0110816","hereditary spastic paraplegia 7","mondo","0011803"
> "2789","parasitic protozoa infectious disease","icd10cm","B50-B64"
> "2789","parasitic protozoa infectious disease","icd10cm","B64"
> "2789","parasitic protozoa infectious disease","mesh","D011528"
> "2789","parasitic protozoa infectious disease","umls","C0033740"
> "2789","parasitic protozoa infectious disease","mondo","0002428"
> "0110817","hereditary spastic paraplegia 72","icd10cm","G11.4"
> "0110817","hereditary spastic paraplegia 72","mondo","0014282"
> "10603","glucose intolerance","icd10cm","R73.03"
> "10603","glucose intolerance","mesh","D018149"
> "10603","glucose intolerance","umls","C0271650"
> "10603","glucose intolerance","mondo","0001076"
> "9467","nail-patella syndrome","icd10cm","Q87.2"
> "9467","nail-patella syndrome","mesh","D009261"
> "9467","nail-patella syndrome","umls","C0027341"
> "9467","nail-patella syndrome","mondo","0008061"
> "2078","chondroid syringoma of the vulva","umls","C1511091"
> "2078","chondroid syringoma of the vulva","mondo","0002199"
> "9461","exposure keratitis","icd10cm","H16.21"
> "9461","exposure keratitis","icd9cm","370.34"
> "9461","exposure keratitis","umls","C0339295"
> "9461","exposure keratitis","mondo","0004794"
> "9460","uterine corpus cancer","icd10cm","C54"
> "9460","uterine corpus cancer","icd10cm","C54.9"
> "9460","uterine corpus cancer","icd9cm","182"
> "9460","uterine corpus cancer","umls","C0153574"
> "9460","uterine corpus cancer","mondo","0006003"
> "9463","otitis externa","icd9cm","380.1"
> "9463","otitis externa","icd9cm","380.10"
> "9463","otitis externa","umls","C0021355"
> "9463","otitis externa","mondo","0004795"
> "9462","cholesteatoma of external ear","icd10cm","H60.4"
> "9462","cholesteatoma of external ear","icd10cm","H60.40"
> "9462","cholesteatoma of external ear","icd9cm","380.21"
> "9462","cholesteatoma of external ear","umls","C0155398"
> "9462","cholesteatoma of external ear","mondo","0006532"
> "2072","vulvar squamous tumor","umls","C1520097"
> "2072","vulvar squamous tumor","mondo","0002195"
> "2071","vulvar squamous papilloma","umls","C1336982"
> "2071","vulvar squamous papilloma","mondo","0002194"
> "0060806","syndromic X-linked intellectual disability Hedera type","mondo","0010319"
> "0111204","distal hereditary motor neuronopathy type 5A","umls","C1833308"
> "11608","fungal meningitis","mesh","D016921"
> "11608","fungal meningitis","umls","C0085438"
> "11608","fungal meningitis","mondo","0006764"
> "2075","minor vestibular glands adenoma","umls","C1510791"
> "2075","minor vestibular glands adenoma","mondo","0002197"
> "2074","intestinal perforation","icd9cm","569.83"
> "2074","intestinal perforation","mesh","D007416"
> "2074","intestinal perforation","umls","C0021845"
> "2074","intestinal perforation","mondo","0006807"
> "14125","abducens nerve neoplasm","umls","C1263898"
> "14125","abducens nerve neoplasm","mondo","0001884"
> "14121","blue toe syndrome","mesh","D018438"
> "14121","blue toe syndrome","umls","C0242645"
> "14121","blue toe syndrome","mondo","0001883"
> "9790","toxocariasis","icd10cm","B83.0"
> "9790","toxocariasis","mesh","D007816"
> "9790","toxocariasis","mesh","D014120"
> "9790","toxocariasis","umls","C0023049"
> "9790","toxocariasis","mondo","0005988"
> "9794","hereditary choroidal atrophy","icd10cm","H31.2"
> "9794","hereditary choroidal atrophy","icd10cm","H31.20"
> "9794","hereditary choroidal atrophy","icd9cm","363.5"
> "9794","hereditary choroidal atrophy","icd9cm","363.50"
> "9794","hereditary choroidal atrophy","umls","C0154893"
> "9794","hereditary choroidal atrophy","mondo","0004883"
> "9799","eye degenerative disease","icd10cm","H44.30"
> "9799","eye degenerative disease","icd10cm","H44.5"
> "9799","eye degenerative disease","icd9cm","360.2"
> "9799","eye degenerative disease","icd9cm","360.20"
> "9799","eye degenerative disease","icd9cm","360.4"
> "9799","eye degenerative disease","icd9cm","360.40"
> "9799","eye degenerative disease","umls","C0154777"
> "9799","eye degenerative disease","mondo","0004884"
> "14384","parietal lobe neoplasm","icd10cm","C71.3"
> "14384","parietal lobe neoplasm","icd9cm","191.3"
> "14384","parietal lobe neoplasm","umls","C0153637"
> "14384","parietal lobe neoplasm","umls","C1263888"
> "14384","parietal lobe neoplasm","mondo","0001952"
> "0110005","Leber congenital amaurosis 9","icd10cm","H35.5"
> "0110005","Leber congenital amaurosis 9","mondo","0012056"
> "0110004","3-methylglutaconic aciduria type 3","mondo","0009787"
> "0110007","achromatopsia 2","mondo","0009003"
> "0110006","3-methylglutaconic aciduria type 4","mondo","0009611"
> "0110001","3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","mondo","0013875"
> "0110000","3-methylglutaconic aciduria type 5","mondo","0012435"
> "0110003","3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia","mondo","0014561"
> "0110002","3-methylglutaconic aciduria type 1","mondo","0009610"
> "0110009","achromatopsia 7","mondo","0014677"
> "0110008","achromatopsia 3","mondo","0009875"
> "0110559","autosomal dominant nonsyndromic deafness 2B","icd10cm","H90.3"
> "0110559","autosomal dominant nonsyndromic deafness 2B","mondo","0012976"
> "0110558","autosomal dominant nonsyndromic deafness 2A","icd10cm","H90.3"
> "0110558","autosomal dominant nonsyndromic deafness 2A","mondo","0010817"
> "12978","Plasmodium vivax malaria","icd10cm","B51"
> "12978","Plasmodium vivax malaria","icd10cm","B51.9"
> "12978","Plasmodium vivax malaria","icd9cm","084.1"
> "12978","Plasmodium vivax malaria","mesh","D016780"
> "12978","Plasmodium vivax malaria","umls","C0024537"
> "12978","Plasmodium vivax malaria","mondo","0005921"
> "12972","intrapelvic lymph node leukemic reticuloendotheliosis","icd9cm","202.46"
> "12972","intrapelvic lymph node leukemic reticuloendotheliosis","umls","C0153831"
> "12972","intrapelvic lymph node leukemic reticuloendotheliosis","mondo","0001607"
> "12971","hereditary spherocytosis","icd10cm","D58.0"
> "12971","hereditary spherocytosis","icd9cm","282.0"
> "12971","hereditary spherocytosis","mesh","D013103"
> "12971","hereditary spherocytosis","umls","C0037889"
> "12971","hereditary spherocytosis","mondo","0019350"
> "7081","lung mixed small cell and squamous cell carcinoma","umls","C1334788"
> "7081","lung mixed small cell and squamous cell carcinoma","mondo","0004100"
> "7086","multicentric papillary thyroid carcinoma","umls","C1334817"
> "7086","multicentric papillary thyroid carcinoma","mondo","0004101"
> "7089","tall cell variant papillary carcinoma","umls","C1336695"
> "7089","tall cell variant papillary carcinoma","mondo","0004103"
> "7088","columnar cell variant papillary carcinoma","umls","C1333120"
> "7088","columnar cell variant papillary carcinoma","mondo","0004102"
> "0060359","Sakati-Nyhan syndrome","icd10cm","Q87.0"
> "0060359","Sakati-Nyhan syndrome","mesh","C537227"
> "0060359","Sakati-Nyhan syndrome","mondo","0007040"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","icd10cm","E71.313"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","mesh","D054069"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C0268596"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C1856401"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C1856403"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C1856405"
> "0060358","multiple acyl-CoA dehydrogenase deficiency","mondo","0009282"
> "0060351","mitochondrial complex III deficiency nuclear type 2","mondo","0014063"
> "0060350","adenine phosphoribosyltransferase deficiency","mesh","C538228"
> "0060350","adenine phosphoribosyltransferase deficiency","umls","C0268120"
> "0060350","adenine phosphoribosyltransferase deficiency","umls","C3665382"
> "0060350","adenine phosphoribosyltransferase deficiency","mondo","0013869"
> "0060353","acrofacial dysostosis Cincinnati type","mondo","0014651"
> "0060352","Kleefstra syndrome","mesh","C563043"
> "0060352","Kleefstra syndrome","umls","C0795833"
> "0060352","Kleefstra syndrome","mondo","0012455"
> "0060355","amyotrophic lateral sclerosis type 22","mondo","0014531"
> "0060354","Stormorken syndrome","mesh","C566108"
> "0060354","Stormorken syndrome","umls","C1861451"
> "0060354","Stormorken syndrome","mondo","0008497"
> "0060357","chylomicron retention disease","icd10cm","E78.3"
> "0060357","chylomicron retention disease","mesh","C535460"
> "0060357","chylomicron retention disease","umls","C0795956"
> "0060357","chylomicron retention disease","mondo","0009528"
> "0060356","Vici syndrome","mesh","C535566"
> "0060356","Vici syndrome","umls","C1855772"
> "0060356","Vici syndrome","mondo","0009452"
> "8170","fibroepithelial polyp of the anus","mondo","0006549"
> "6494","pediatric myxoid chondrosarcoma","umls","C1332984"
> "6494","pediatric myxoid chondrosarcoma","mondo","0003898"
> "6496","extraskeletal myxoid chondrosarcoma","mesh","C563195"
> "6496","extraskeletal myxoid chondrosarcoma","umls","C1275278"
> "6496","extraskeletal myxoid chondrosarcoma","mondo","0012825"
> "6491","breast capillary hemangioma","umls","C1332619"
> "6491","breast capillary hemangioma","mondo","0003896"
> "6492","breast epithelioid hemangioma","umls","C1332627"
> "6492","breast epithelioid hemangioma","mondo","0003897"
> "8178","endometrial type cervical adenomyoma","umls","C1516406"
> "8178","endometrial type cervical adenomyoma","mondo","0004487"
> "8179","cervical atypical polypoid adenomyoma","umls","C1516409"
> "8179","cervical atypical polypoid adenomyoma","mondo","0004488"
> "6498","seborrheic keratosis","icd10cm","L82"
> "6498","seborrheic keratosis","icd10cm","L82.1"
> "6498","seborrheic keratosis","icd9cm","702.1"
> "6498","seborrheic keratosis","mesh","D017492"
> "6498","seborrheic keratosis","umls","C0022603"
> "6498","seborrheic keratosis","mondo","0008420"
> "6948","malignant gastric teratoma","umls","C1334151"
> "6948","malignant gastric teratoma","mondo","0004048"
> "6943","vulvar inverted follicular keratosis","umls","C1520084"
> "6943","vulvar inverted follicular keratosis","mondo","0006621"
> "6947","sphenoidal sinus neoplasm","umls","C0345676"
> "6947","sphenoidal sinus neoplasm","mondo","0004047"
> "6945","inverted follicular keratosis","umls","C0334019"
> "6945","inverted follicular keratosis","mondo","0006563"
> "6944","vulvar seborrheic keratosis","umls","C1336981"
> "6944","vulvar seborrheic keratosis","mondo","0006622"
> "0060135","apraxia","mondo","0000665"
> "8398","osteoarthritis","icd9cm","715.3"
> "8398","osteoarthritis","mesh","D010003"
> "8398","osteoarthritis","umls","C0157946"
> "8398","osteoarthritis","mondo","0005178"
> "8399","trombiculiasis","mesh","D014323"
> "8399","trombiculiasis","umls","C0041170"
> "8399","trombiculiasis","mondo","0005998"
> "8394","adult type testicular granulosa cell tumor","umls","C1515284"
> "8394","adult type testicular granulosa cell tumor","mondo","0004548"
> "13921","bacterial esophagitis","umls","C0341108"
> "13921","bacterial esophagitis","mondo","0001832"
> "8392","reticular pattern testicular yolk sac tumor","umls","C1515308"
> "8392","reticular pattern testicular yolk sac tumor","mondo","0004547"
> "4398","pustulosis of palm and sole","icd10cm","L40.3"
> "4398","pustulosis of palm and sole","mesh","D011565"
> "4398","pustulosis of palm and sole","umls","C0030246"
> "4398","pustulosis of palm and sole","mondo","0002985"
> "4399","acneiform dermatitis","umls","C0234894"
> "4399","acneiform dermatitis","mondo","0006521"
> "4394","reticulohistiocytic granuloma","mesh","D015616"
> "4394","reticulohistiocytic granuloma","umls","C0035290"
> "4394","reticulohistiocytic granuloma","mondo","0002984"
> "4397","granulomatous dermatitis","umls","C0743086"
> "4397","granulomatous dermatitis","mondo","0006555"
> "472","subglottic angioma","umls","C1336518"
> "472","subglottic angioma","mondo","0003115"
> "3196","cellular schwannoma","umls","C0431124"
> "3196","cellular schwannoma","mondo","0002548"
> "470","verrucous keratotic hemangioma","umls","C0334540"
> "470","verrucous keratotic hemangioma","mondo","0003106"
> "471","skin hemangioma","umls","C0687140"
> "471","skin hemangioma","mondo","0003110"
> "476","breast hemangioma","umls","C0853715"
> "476","breast hemangioma","mondo","0003126"
> "1363","ethmoid sinus cancer","icd10cm","C31.1"
> "1363","ethmoid sinus cancer","icd9cm","160.3"
> "1363","ethmoid sinus cancer","umls","C0153477"
> "1363","ethmoid sinus cancer","mondo","0001763"
> "474","histiocytoid hemangioma","mesh","D006391"
> "474","histiocytoid hemangioma","umls","C0205788"
> "474","histiocytoid hemangioma","mondo","0003119"
> "1361","frontal sinus neoplasm","umls","C0345672"
> "1361","frontal sinus neoplasm","mondo","0001757"
> "479","angiokeratoma","mesh","D000794"
> "479","angiokeratoma","umls","C0002985"
> "479","angiokeratoma","umls","C0346075"
> "479","angiokeratoma","mondo","0003143"
> "3199","C-P angle neurinoma","umls","C1332905"
> "3199","C-P angle neurinoma","mondo","0002551"
> "3198","hypoglossal nerve neoplasm","umls","C1263903"
> "3198","hypoglossal nerve neoplasm","mondo","0002550"
> "0050439","Usher syndrome","mesh","D052245"
> "0050439","Usher syndrome","umls","C0271097"
> "0050439","Usher syndrome","umls","C1568248"
> "0050439","Usher syndrome","umls","C1568249"
> "0050439","Usher syndrome","umls","C2931205"
> "0050439","Usher syndrome","mondo","0019501"
2232,2244c6388,7514
< "0070257","congenital disorder of glycosylation type IIe","umls","C2931010"
< "0070257","congenital disorder of glycosylation type IIe","mondo","0010490"
< "0070256","congenital disorder of glycosylation type IId","umls","C2931009"
< "0070256","congenital disorder of glycosylation type IId","mondo","0011772"
< "0070259","congenital disorder of glycosylation type IIg","umls","C2931011"
< "0070259","congenital disorder of glycosylation type IIg","mondo","0012637"
< "0070258","congenital disorder of glycosylation type IIf","umls","C1970344"
< "0070258","congenital disorder of glycosylation type IIf","mondo","0011342"
< "1975","thymus lipoma","umls","C1336744"
< "1975","thymus lipoma","mondo","0002163"
< "1974","adenosarcoma","mesh","D018195"
< "1974","adenosarcoma","umls","C0001442"
< "1974","adenosarcoma","mondo","0005636"
---
> "13736","uterine inflammatory disease","icd10cm","N71.9"
> "13736","uterine inflammatory disease","icd9cm","615.9"
> "13736","uterine inflammatory disease","umls","C0269047"
> "13736","uterine inflammatory disease","mondo","0001786"
> "4024","scirrhous adenocarcinoma","mesh","D002293"
> "4024","scirrhous adenocarcinoma","umls","C0007135"
> "4024","scirrhous adenocarcinoma","mondo","0005953"
> "4025","obsolete steatitis","mesh","D013231"
> "4025","obsolete steatitis","umls","C0038235"
> "4025","obsolete steatitis","mondo","0006979"
> "4022","ureterocele","mesh","D014518"
> "4022","ureterocele","umls","C0041960"
> "4022","ureterocele","mondo","0008628"
> "4023","linitis plastica","mesh","D008039"
> "4023","linitis plastica","umls","C0023743"
> "4023","linitis plastica","mondo","0002839"
> "13731","malignant secondary hypertension","icd9cm","405.0"
> "13731","malignant secondary hypertension","umls","C0155617"
> "13731","malignant secondary hypertension","mondo","0001785"
> "4028","angioma serpiginosum","icd10cm","L81.7"
> "4028","angioma serpiginosum","mesh","C536366"
> "4028","angioma serpiginosum","umls","C0263637"
> "4028","angioma serpiginosum","mondo","0019803"
> "4029","gastritis","icd10cm","K29.7"
> "4029","gastritis","mesh","D005756"
> "4029","gastritis","umls","C0017152"
> "4029","gastritis","mondo","0004966"
> "11382","corneal neovascularization","icd10cm","H16.4"
> "11382","corneal neovascularization","icd10cm","H16.40"
> "11382","corneal neovascularization","icd9cm","370.6"
> "11382","corneal neovascularization","icd9cm","370.60"
> "11382","corneal neovascularization","mesh","D016510"
> "11382","corneal neovascularization","umls","C0085109"
> "11382","corneal neovascularization","mondo","0006713"
> "11383","cryptorchidism","icd10cm","Q53.9"
> "11383","cryptorchidism","icd9cm","752.51"
> "11383","cryptorchidism","mesh","D003456"
> "11383","cryptorchidism","umls","C0010417"
> "11383","cryptorchidism","mondo","0009047"
> "11385","expressive language disorder","icd10cm","F80.1"
> "11385","expressive language disorder","icd9cm","315.31"
> "11385","expressive language disorder","umls","C0236826"
> "11385","expressive language disorder","mondo","0001276"
> "11387","epidural abscess","mesh","D020802"
> "11387","epidural abscess","umls","C0270629"
> "11387","epidural abscess","mondo","0005752"
> "11389","subdural empyema","mesh","D013354"
> "11389","subdural empyema","umls","C0038539"
> "11389","subdural empyema","mondo","0006984"
> "13295","crater-like holes of optic disc","icd9cm","377.22"
> "13295","crater-like holes of optic disc","umls","C0155298"
> "13295","crater-like holes of optic disc","mondo","0001679"
> "1659","supratentorial cancer","icd10cm","C71.0"
> "1659","supratentorial cancer","mesh","D015173"
> "1659","supratentorial cancer","umls","C0038874"
> "1659","supratentorial cancer","umls","C0751589"
> "1659","supratentorial cancer","mondo","0002071"
> "3999","Bartholin's gland carcinoma","umls","C0349561"
> "3999","Bartholin's gland carcinoma","mondo","0002829"
> "3998","Bartholin's gland transitional cell carcinoma","umls","C1511053"
> "3998","Bartholin's gland transitional cell carcinoma","mondo","0002828"
> "3996","urinary system cancer","icd10cm","C68.9"
> "3996","urinary system cancer","icd9cm","189.9"
> "3996","urinary system cancer","umls","C0348371"
> "3996","urinary system cancer","mondo","0006295"
> "0110204","Charcot-Marie-Tooth disease recessive intermediate B","icd10cm","G60.0"
> "0110204","Charcot-Marie-Tooth disease recessive intermediate B","mondo","0013338"
> "298","lacrimal gland adenocarcinoma","umls","C0346341"
> "298","lacrimal gland adenocarcinoma","mondo","0002475"
> "299","adenocarcinoma","mesh","D000230"
> "299","adenocarcinoma","umls","C0001418"
> "299","adenocarcinoma","mondo","0004970"
> "296","mixed lacrimal gland cancer","umls","C0346342"
> "296","mixed lacrimal gland cancer","mondo","0002469"
> "297","pleomorphic adenoma carcinoma","umls","C0344460"
> "297","pleomorphic adenoma carcinoma","mondo","0006403"
> "294","lacrimal gland cancer","icd9cm","190.2"
> "294","lacrimal gland cancer","umls","C0153627"
> "294","lacrimal gland cancer","umls","C0339124"
> "294","lacrimal gland cancer","mondo","0002464"
> "295","eye carcinoma","umls","C0848866"
> "295","eye carcinoma","mondo","0002466"
> "292","lacrimal system cancer","umls","C1334361"
> "292","lacrimal system cancer","mondo","0002460"
> "293","lacrimal gland carcinoma","umls","C1334358"
> "293","lacrimal gland carcinoma","mondo","0002463"
> "2441","frontal sinus squamous cell carcinoma","umls","C1333646"
> "2441","frontal sinus squamous cell carcinoma","mondo","0002301"
> "2444","hyperpituitarism","mesh","D006964"
> "2444","hyperpituitarism","umls","C0020506"
> "2444","hyperpituitarism","mondo","0006793"
> "12524","plantar nerve lesion","icd10cm","G57.6"
> "12524","plantar nerve lesion","icd10cm","G57.60"
> "12524","plantar nerve lesion","icd9cm","355.6"
> "12524","plantar nerve lesion","umls","C0154752"
> "12524","plantar nerve lesion","mondo","0001541"
> "2449","acromegaly","mesh","D000172"
> "2449","acromegaly","umls","C0001206"
> "2449","acromegaly","mondo","0019933"
> "7867","adult central nervous system germinoma","umls","C1370504"
> "7867","adult central nervous system germinoma","mondo","0004383"
> "0070059","autosomal dominant non-syndromic intellectual disability 29","mondo","0014482"
> "0070058","Helsmoortel-Van Der Aa Syndrome","mondo","0014379"
> "0070057","autosomal dominant non-syndromic intellectual disability 27","mondo","0014376"
> "0070056","autosomal dominant non-syndromic intellectual disability 26","mondo","0014361"
> "0070055","Xia-Gibbs Syndrome","mondo","0014358"
> "0070054","autosomal dominant non-syndromic intellectual disability 24","mondo","0014357"
> "0070053","autosomal dominant non-syndromic intellectual disability 23","mondo","0014336"
> "0070052","autosomal dominant non-syndromic intellectual disability 22","mondo","0012869"
> "0070051","autosomal dominant non-syndromic intellectual disability 21","mondo","0014213"
> "0070050","autosomal dominant mental retardation 20","mondo","0013266"
> "0110638","congenital muscular dystrophy merosin-positive","mondo","0012279"
> "0110639","congenital muscular dystrophy due to integrin alpha-7 deficiency","icd10cm","G71.2"
> "0110639","congenital muscular dystrophy due to integrin alpha-7 deficiency","mondo","0013177"
> "0110632","megaconial type congenital muscular dystrophy","icd10cm","G71.2"
> "0110632","megaconial type congenital muscular dystrophy","mondo","0011246"
> "0110633","rigid spine muscular dystrophy 1","icd10cm","G71.2"
> "0110633","rigid spine muscular dystrophy 1","icd10cm","G71.8"
> "0110633","rigid spine muscular dystrophy 1","mesh","C535683"
> "0110633","rigid spine muscular dystrophy 1","mondo","0011271"
> "0110630","Wolfram syndrome 2","icd10cm","E13.8"
> "0110630","Wolfram syndrome 2","mondo","0011502"
> "0110631","arthrogryposis due to muscular dystrophy","icd10cm","M62.8"
> "0110631","arthrogryposis due to muscular dystrophy","mondo","0009679"
> "0110636","congenital merosin-deficient muscular dystrophy 1A","mesh","C537384"
> "0110636","congenital merosin-deficient muscular dystrophy 1A","umls","C1263858"
> "0110636","congenital merosin-deficient muscular dystrophy 1A","mondo","0011925"
> "0110637","muscular dystrophy-dystroglycanopathy type B6","icd10cm","G71.2"
> "0110637","muscular dystrophy-dystroglycanopathy type B6","mondo","0012138"
> "0110634","congenital muscular dystrophy 1B","icd10cm","G71.2"
> "0110634","congenital muscular dystrophy 1B","mondo","0011486"
> "0110635","muscular dystrophy-dystroglycanopathy type B5","icd10cm","G71.2"
> "0110635","muscular dystrophy-dystroglycanopathy type B5","mondo","0011688"
> "12129","bulimia nervosa","icd10cm","F50.2"
> "12129","bulimia nervosa","mesh","D002032"
> "12129","bulimia nervosa","mesh","D052018"
> "12129","bulimia nervosa","umls","C0006370"
> "12129","bulimia nervosa","mondo","0005452"
> "6379","diffuse meningeal melanocytosis","umls","C1266112"
> "6379","diffuse meningeal melanocytosis","mondo","0003867"
> "6370","hepatic osteogenic sarcoma","umls","C1333974"
> "6370","hepatic osteogenic sarcoma","mondo","0003866"
> "12120","pulmonary alveolar proteinosis","icd10cm","J84.01"
> "12120","pulmonary alveolar proteinosis","icd9cm","516.0"
> "12120","pulmonary alveolar proteinosis","mesh","D011649"
> "12120","pulmonary alveolar proteinosis","umls","C0034050"
> "12120","pulmonary alveolar proteinosis","mondo","0001437"
> "12123","postinflammatory pulmonary fibrosis","icd10cm","J84.10"
> "12123","postinflammatory pulmonary fibrosis","icd9cm","515"
> "12123","postinflammatory pulmonary fibrosis","umls","C0175999"
> "12123","postinflammatory pulmonary fibrosis","mondo","0001438"
> "0111140","IGSF1 deficiency syndrome","icd10cm","E03.1"
> "0111140","IGSF1 deficiency syndrome","mondo","0010475"
> "12125","neurotrophic keratoconjunctivitis","icd10cm","H16.23"
> "12125","neurotrophic keratoconjunctivitis","icd9cm","370.35"
> "12125","neurotrophic keratoconjunctivitis","umls","C0155084"
> "12125","neurotrophic keratoconjunctivitis","mondo","0001440"
> "12124","episcleritis periodica fugax","icd10cm","H15.11"
> "12124","episcleritis periodica fugax","icd9cm","379.01"
> "12124","episcleritis periodica fugax","umls","C0155351"
> "12124","episcleritis periodica fugax","mondo","0001439"
> "6376","hypersplenism","icd10cm","D73.1"
> "6376","hypersplenism","icd9cm","289.4"
> "6376","hypersplenism","mesh","D006971"
> "6376","hypersplenism","umls","C0020532"
> "6376","hypersplenism","mondo","0006795"
> "10140","dry eye syndrome","icd10cm","H04.12"
> "10140","dry eye syndrome","mesh","D015352"
> "10140","dry eye syndrome","umls","C0013238"
> "10140","dry eye syndrome","mondo","0006733"
> "0111549","aplasia of lacrimal and salivary glands","mesh","C562407"
> "0111549","aplasia of lacrimal and salivary glands","umls","C0158667"
> "0111548","ring dermoid of cornea","mesh","C535684"
> "0111548","ring dermoid of cornea","umls","C1867155"
> "10146","thymus lymphoma","umls","C1336745"
> "10146","thymus lymphoma","mondo","0000951"
> "10149","long bones of lower limb cancer","icd10cm","C40.2"
> "10149","long bones of lower limb cancer","icd9cm","170.7"
> "10149","long bones of lower limb cancer","umls","C0153517"
> "10149","long bones of lower limb cancer","mondo","0000952"
> "0111542","familial expansile osteolysis","mesh","C536335"
> "0111542","familial expansile osteolysis","umls","C0432292"
> "0111541","pigmented paravenous chorioretinal atrophy","mesh","C566801"
> "0111541","pigmented paravenous chorioretinal atrophy","umls","C1868310"
> "12997","Phlegmonous dacryocystitis","icd10cm","H04.31"
> "12997","Phlegmonous dacryocystitis","icd9cm","375.33"
> "12997","Phlegmonous dacryocystitis","umls","C0155238"
> "12997","Phlegmonous dacryocystitis","mondo","0001611"
> "0111546","Currarino syndrome","mesh","C536221"
> "0111546","Currarino syndrome","umls","C1531773"
> "0111545","familial male-limited precocious puberty","mesh","C536961"
> "0111545","familial male-limited precocious puberty","umls","C0342549"
> "0111545","familial male-limited precocious puberty","umls","C1504412"
> "0111544","Guttmacher syndrome","mesh","C538278"
> "0111544","Guttmacher syndrome","umls","C1867801"
> "0110496","autosomal recessive nonsyndromic deafness 38","icd10cm","H90.3"
> "0110496","autosomal recessive nonsyndromic deafness 38","mondo","0011991"
> "0110497","autosomal recessive nonsyndromic deafness 39","icd10cm","H90.3"
> "0110497","autosomal recessive nonsyndromic deafness 39","mondo","0012003"
> "0110494","autosomal recessive nonsyndromic deafness 36","icd10cm","H90.3"
> "0110494","autosomal recessive nonsyndromic deafness 36","mondo","0012170"
> "0110495","autosomal recessive nonsyndromic deafness 37","icd10cm","H90.3"
> "0110495","autosomal recessive nonsyndromic deafness 37","mondo","0011912"
> "0110492","autosomal recessive nonsyndromic deafness 33","icd10cm","H90.3"
> "0110492","autosomal recessive nonsyndromic deafness 33","mondo","0011799"
> "0110493","autosomal recessive nonsyndromic deafness 35","icd10cm","H90.3"
> "0110493","autosomal recessive nonsyndromic deafness 35","mondo","0012060"
> "0110490","autosomal recessive nonsyndromic deafness 31","icd10cm","H90.3"
> "0110490","autosomal recessive nonsyndromic deafness 31","mondo","0011767"
> "0110491","autosomal recessive nonsyndromic deafness 32","icd10cm","H90.3"
> "0110491","autosomal recessive nonsyndromic deafness 32","mondo","0012091"
> "9631","Pelger-Huet anomaly","mesh","D010381"
> "9631","Pelger-Huet anomaly","umls","C0030779"
> "9631","Pelger-Huet anomaly","mondo","0008214"
> "0110498","autosomal recessive nonsyndromic deafness 4","icd10cm","H90.3"
> "0110498","autosomal recessive nonsyndromic deafness 4","mondo","0010933"
> "9637","stomatitis","icd10cm","K12.1"
> "9637","stomatitis","mesh","D013280"
> "9637","stomatitis","umls","C0038362"
> "9637","stomatitis","mondo","0004842"
> "8941","seborrheic infantile dermatitis","icd10cm","L21.0"
> "8941","seborrheic infantile dermatitis","icd9cm","690.11"
> "8941","seborrheic infantile dermatitis","mesh","D063807"
> "8941","seborrheic infantile dermatitis","umls","C0221244"
> "8941","seborrheic infantile dermatitis","mondo","0006609"
> "8943","lattice corneal dystrophy","mesh","C537935"
> "8943","lattice corneal dystrophy","mondo","0004686"
> "8947","diabetic retinopathy","icd9cm","362.0"
> "8947","diabetic retinopathy","mesh","D003930"
> "8947","diabetic retinopathy","umls","C0011884"
> "8947","diabetic retinopathy","mondo","0005266"
> "8946","severe nonproliferative diabetic retinopathy","icd9cm","362.06"
> "8946","severe nonproliferative diabetic retinopathy","umls","C0730278"
> "8946","severe nonproliferative diabetic retinopathy","mondo","0004687"
> "1436","corneal ectasia","icd10cm","H18.71"
> "1436","corneal ectasia","icd9cm","371.71"
> "1436","corneal ectasia","umls","C0155135"
> "1436","corneal ectasia","mondo","0001950"
> "3390","palmoplantar keratosis","icd10cm","L85.2"
> "3390","palmoplantar keratosis","mesh","D007645"
> "3390","palmoplantar keratosis","umls","C0022596"
> "3390","palmoplantar keratosis","mondo","0006590"
> "1432","blindness","icd10cm","H54"
> "1432","blindness","icd9cm","369"
> "1432","blindness","mesh","D001766"
> "1432","blindness","umls","C0155020"
> "1432","blindness","mondo","0001941"
> "5182","blastema predominant kidney Wilms' tumor","umls","C0279609"
> "5182","blastema predominant kidney Wilms' tumor","mondo","0003320"
> "3206","plexiform schwannoma","umls","C1370659"
> "3206","plexiform schwannoma","mondo","0002559"
> "3205","melanotic neurilemmoma","umls","C1306247"
> "3205","melanotic neurilemmoma","mondo","0002558"
> "3204","neurilemmomatosis","icd10cm","Q85.03"
> "3204","neurilemmomatosis","icd9cm","237.73"
> "3204","neurilemmomatosis","mesh","C536641"
> "3204","neurilemmomatosis","umls","C1335929"
> "3204","neurilemmomatosis","mondo","0008075"
> "3203","macrocystic neurilemmoma","umls","C4054526"
> "3203","macrocystic neurilemmoma","mondo","0024657"
> "3202","neurilemmoma of the fifth cranial nerve","umls","C0349582"
> "3202","neurilemmoma of the fifth cranial nerve","mondo","0002555"
> "3201","sympathetic neurilemmoma","umls","C1336543"
> "3201","sympathetic neurilemmoma","mondo","0002554"
> "1996","rectum adenocarcinoma","umls","C0149978"
> "1996","rectum adenocarcinoma","mondo","0002169"
> "1999","chronic eustachian salpingitis","icd10cm","H68.02"
> "1999","chronic eustachian salpingitis","icd10cm","H68.029"
> "1999","chronic eustachian salpingitis","icd9cm","381.52"
> "1999","chronic eustachian salpingitis","umls","C0155430"
> "1999","chronic eustachian salpingitis","mondo","0002170"
> "1998","Lutembacher's syndrome","mesh","D008185"
> "1998","Lutembacher's syndrome","umls","C0024164"
> "1998","Lutembacher's syndrome","mondo","0006839"
> "1629","breast myofibroblastoma","umls","C1511320"
> "1629","breast myofibroblastoma","mondo","0002062"
> "5189","epithelial predominant Wilms' tumor","umls","C0279608"
> "5189","epithelial predominant Wilms' tumor","mondo","0003322"
> "3209","junctional epidermolysis bullosa","mesh","D016109"
> "3209","junctional epidermolysis bullosa","umls","C0079301"
> "3209","junctional epidermolysis bullosa","mondo","0017612"
> "14720","type I Ehlers-Danlos syndrome","mesh","C536194"
> "14720","type I Ehlers-Danlos syndrome","umls","C0268335"
> "14720","type I Ehlers-Danlos syndrome","mondo","0019567"
> "3535","Unverricht-Lundborg syndrome","mesh","D020194"
> "3535","Unverricht-Lundborg syndrome","umls","C0751785"
> "3535","Unverricht-Lundborg syndrome","mondo","0009698"
> "14723","beta-ketothiolase deficiency","mesh","C535818"
> "14723","beta-ketothiolase deficiency","umls","C1533628"
> "14723","beta-ketothiolase deficiency","mondo","0008760"
> "3534","Lafora disease","mesh","D020192"
> "3534","Lafora disease","umls","C0751783"
> "3534","Lafora disease","mondo","0009697"
> "2860","hemoglobinopathy","icd10cm","D58.2"
> "2860","hemoglobinopathy","mesh","D006453"
> "2860","hemoglobinopathy","umls","C0019045"
> "2860","hemoglobinopathy","mondo","0019050"
> "2861","congenital nonspherocytic hemolytic anemia","mesh","D000746"
> "2861","congenital nonspherocytic hemolytic anemia","umls","C0002882"
> "2861","congenital nonspherocytic hemolytic anemia","mondo","0006506"
> "2862","glucosephosphate dehydrogenase deficiency","mesh","D005955"
> "2862","glucosephosphate dehydrogenase deficiency","umls","C2939465"
> "2862","glucosephosphate dehydrogenase deficiency","mondo","0005775"
> "559","acute pyelonephritis","icd10cm","N10"
> "559","acute pyelonephritis","icd9cm","590.1"
> "559","acute pyelonephritis","umls","C0520575"
> "559","acute pyelonephritis","mondo","0003529"
> "14725","autosomal dominant microcephaly","mesh","C537323"
> "14725","autosomal dominant microcephaly","umls","C0220693"
> "14725","autosomal dominant microcephaly","mondo","0007988"
> "557","kidney disease","icd10cm","N08"
> "557","kidney disease","icd10cm","N28.9"
> "557","kidney disease","mesh","D007674"
> "557","kidney disease","umls","C0022658"
> "557","kidney disease","mondo","0005240"
> "551","toxic pneumonitis","icd9cm","506.9"
> "551","toxic pneumonitis","umls","C0041881"
> "551","toxic pneumonitis","mondo","0003479"
> "552","pneumonia","mesh","D011014"
> "552","pneumonia","umls","C0032285"
> "552","pneumonia","mondo","0005249"
> "14247","chronic purulent otitis media","icd10cm","H66.3"
> "14247","chronic purulent otitis media","icd9cm","382.3"
> "14247","chronic purulent otitis media","umls","C0271454"
> "14247","chronic purulent otitis media","mondo","0001920"
> "14244","epiphora due to excess lacrimation","icd10cm","H04.21"
> "14244","epiphora due to excess lacrimation","icd9cm","375.21"
> "14244","epiphora due to excess lacrimation","umls","C0155233"
> "14244","epiphora due to excess lacrimation","mondo","0001918"
> "14245","cystoid macular retinal degeneration","icd10cm","H35.35"
> "14245","cystoid macular retinal degeneration","icd9cm","362.53"
> "14245","cystoid macular retinal degeneration","umls","C0154850"
> "14245","cystoid macular retinal degeneration","mondo","0001919"
> "5409","lung small cell carcinoma","kegg","05222"
> "5409","lung small cell carcinoma","mesh","D055752"
> "5409","lung small cell carcinoma","umls","C0149925"
> "5409","lung small cell carcinoma","mondo","0008433"
> "14717","centronuclear myopathy","mesh","D020914"
> "14717","centronuclear myopathy","umls","C0175709"
> "14717","centronuclear myopathy","mondo","0018947"
> "1439","pyuria","mesh","D011776"
> "1439","pyuria","umls","C0034359"
> "1439","pyuria","mondo","0001953"
> "5056","adult cerebellar neoplasm","umls","C1332197"
> "5056","adult cerebellar neoplasm","mondo","0003260"
> "14248","chronic atticoantral disease","icd10cm","H66.2"
> "14248","chronic atticoantral disease","icd10cm","H66.20"
> "14248","chronic atticoantral disease","icd9cm","382.2"
> "14248","chronic atticoantral disease","umls","C0155441"
> "14248","chronic atticoantral disease","mondo","0001921"
> "5057","papillary meningioma of the cerebellum","umls","C1332902"
> "5057","papillary meningioma of the cerebellum","mondo","0003261"
> "3342","bone inflammation disease","mesh","D010000"
> "3342","bone inflammation disease","umls","C0029400"
> "3342","bone inflammation disease","mondo","0002614"
> "3343","glycoproteinosis","mesh","D009081"
> "3343","glycoproteinosis","umls","C0026697"
> "3343","glycoproteinosis","mondo","0009738"
> "1192","peripheral nervous system neoplasm","mesh","D010524"
> "1192","peripheral nervous system neoplasm","mesh","D018317"
> "1192","peripheral nervous system neoplasm","umls","C0031118"
> "1192","peripheral nervous system neoplasm","umls","C0206727"
> "1192","peripheral nervous system neoplasm","mondo","0001406"
> "1195","ischemic neuropathy","umls","C0238309"
> "1195","ischemic neuropathy","mondo","0001408"
> "3347","osteosarcoma","mesh","D012516"
> "3347","osteosarcoma","mesh","D018213"
> "3347","osteosarcoma","umls","C0029463"
> "3347","osteosarcoma","umls","C0206639"
> "3347","osteosarcoma","mondo","0009807"
> "3345","xanthomatosis","mesh","D014973"
> "3345","xanthomatosis","umls","C0043325"
> "3345","xanthomatosis","mondo","0002615"
> "0050655","Bamforth-Lazarus syndrome","mondo","0009437"
> "13948","bladder neck obstruction","icd10cm","N32.0"
> "13948","bladder neck obstruction","icd9cm","596.0"
> "13948","bladder neck obstruction","mesh","D001748"
> "13948","bladder neck obstruction","umls","C0005694"
> "13948","bladder neck obstruction","mondo","0006679"
> "4258","Weissenbacher-Zweymuller syndrome","icd10cm","Q87.0"
> "4258","Weissenbacher-Zweymuller syndrome","mesh","D010855"
> "4258","Weissenbacher-Zweymuller syndrome","umls","C0031900"
> "4258","Weissenbacher-Zweymuller syndrome","mondo","0010195"
> "4251","conjunctival disease","icd10cm","H10-H11"
> "4251","conjunctival disease","icd10cm","H11.9"
> "4251","conjunctival disease","icd9cm","372"
> "4251","conjunctival disease","icd9cm","372.9"
> "4251","conjunctival disease","mesh","D003229"
> "4251","conjunctival disease","umls","C0009759"
> "4250","conjunctivochalasis","icd10cm","H11.82"
> "4250","conjunctivochalasis","icd9cm","372.81"
> "4250","conjunctivochalasis","umls","C0878693"
> "4250","conjunctivochalasis","mondo","0002931"
> "4253","melorheostosis","mesh","D008557"
> "4253","melorheostosis","umls","C0025239"
> "4253","melorheostosis","mondo","0007970"
> "4252","Alexander disease","mesh","D038261"
> "4252","Alexander disease","umls","C0270726"
> "4252","Alexander disease","mondo","0008752"
> "4254","osteosclerosis","icd10cm","Q78.2"
> "4254","osteosclerosis","mesh","D010026"
> "4254","osteosclerosis","umls","C0029464"
> "4254","osteosclerosis","mondo","0002933"
> "4257","Caffey disease","icd10cm","M89.8"
> "4257","Caffey disease","mesh","D006958"
> "4257","Caffey disease","umls","C0020497"
> "4257","Caffey disease","mondo","0007244"
> "5533","endometrial squamous cell carcinoma","umls","C1333396"
> "5533","endometrial squamous cell carcinoma","mondo","0006198"
> "5532","ovarian squamous cell neoplasm","umls","C1518739"
> "5532","ovarian squamous cell neoplasm","mondo","0003495"
> "5531","ovarian squamous cell carcinoma","mondo","0003494"
> "5530","thymus squamous cell carcinoma","umls","C1336082"
> "5530","thymus squamous cell carcinoma","mondo","0003493"
> "5537","squamous cell bile duct carcinoma","umls","C0861861"
> "5537","squamous cell bile duct carcinoma","mondo","0003500"
> "5536","sarcomatoid squamous cell skin carcinoma","umls","C0349656"
> "5536","sarcomatoid squamous cell skin carcinoma","mondo","0003499"
> "5535","gallbladder squamous cell carcinoma","umls","C0279658"
> "5535","gallbladder squamous cell carcinoma","mondo","0006220"
> "5534","renal pelvis squamous cell carcinoma","umls","C0238409"
> "5534","renal pelvis squamous cell carcinoma","mondo","0003497"
> "5539","ureter squamous cell carcinoma","umls","C1336879"
> "5539","ureter squamous cell carcinoma","mondo","0003502"
> "5538","external ear squamous cell carcinoma","umls","C1333494"
> "5538","external ear squamous cell carcinoma","mondo","0003501"
> "0110149","Charcot-Marie-Tooth disease type 1F","icd10cm","G60.0"
> "0110149","Charcot-Marie-Tooth disease type 1F","mondo","0011902"
> "0060597","atypical chronic myeloid leukemia","icd10cm","C92.2"
> "0060597","atypical chronic myeloid leukemia","icd10cm","C92.20"
> "0060597","atypical chronic myeloid leukemia","mesh","D054438"
> "0060597","atypical chronic myeloid leukemia","umls","C1292772"
> "0060597","atypical chronic myeloid leukemia","mondo","0020312"
> "0060650","dicarboxylic aminoaciduria","mesh","C536171"
> "0060650","dicarboxylic aminoaciduria","umls","C1857253"
> "0060650","dicarboxylic aminoaciduria","mondo","0009110"
> "0060651","MYH-9 related disease","icd10cm","D69.4"
> "0060651","MYH-9 related disease","mondo","0015912"
> "0060652","familial erythrocytosis 1","icd10cm","D75.0"
> "0060652","familial erythrocytosis 1","mondo","0007572"
> "0060653","lethal congenital contracture syndrome 3","mondo","0012656"
> "0060654","lethal congenital contracture syndrome 4","mondo","0013965"
> "0060655","autosomal recessive congenital ichthyosis","mesh","D016113"
> "0060655","autosomal recessive congenital ichthyosis","mesh","D017490"
> "0060655","autosomal recessive congenital ichthyosis","umls","C0079154"
> "0060655","autosomal recessive congenital ichthyosis","mondo","0017265"
> "0060656","autosomal recessive congenital ichthyosis 1","icd10cm","Q80.2"
> "0060656","autosomal recessive congenital ichthyosis 1","mondo","0009441"
> "13972","female breast lower-outer quadrant cancer","icd10cm","C50.51"
> "13972","female breast lower-outer quadrant cancer","icd9cm","174.5"
> "13972","female breast lower-outer quadrant cancer","umls","C0153553"
> "13972","female breast lower-outer quadrant cancer","mondo","0001850"
> "4265","angiomyoma","mesh","D018229"
> "4265","angiomyoma","umls","C0206653"
> "4265","angiomyoma","mondo","0006646"
> "6576","childhood optic nerve glioma","mesh","D020339"
> "6576","childhood optic nerve glioma","umls","C0278653"
> "6576","childhood optic nerve glioma","mondo","0003932"
> "0060591","WHIM syndrome","mesh","C536697"
> "0060591","WHIM syndrome","umls","C0472817"
> "0060591","WHIM syndrome","mondo","0008674"
> "6575","childhood optic tract astrocytoma","umls","C1333014"
> "6575","childhood optic tract astrocytoma","mondo","0003931"
> "6579","chest wall bone cancer","umls","C1334572"
> "6579","chest wall bone cancer","mondo","0003933"
> "0111369","hyperalphalipoproteinemia 1","mesh","C564591"
> "0111369","hyperalphalipoproteinemia 1","umls","C0342883"
> "7694","bladder urachal adenocarcinoma","umls","C1511204"
> "7694","bladder urachal adenocarcinoma","mondo","0004331"
> "1340","pure red-cell aplasia","mesh","D012010"
> "1340","pure red-cell aplasia","umls","C0034902"
> "1340","pure red-cell aplasia","mondo","0001705"
> "7696","lung hilum cancer","umls","C0346601"
> "7696","lung hilum cancer","mondo","0004332"
> "7697","pancreatic ACTH hormone producing tumor","umls","C1335300"
> "7697","pancreatic ACTH hormone producing tumor","mondo","0004333"
> "7693","abdominal aortic aneurysm","mesh","D017544"
> "7693","abdominal aortic aneurysm","umls","C0162871"
> "7693","abdominal aortic aneurysm","mondo","0005350"
> "7698","non-functioning pancreatic endocrine tumor","mesh","C536126"
> "7698","non-functioning pancreatic endocrine tumor","umls","C1334977"
> "7698","non-functioning pancreatic endocrine tumor","mondo","0004334"
> "1342","congenital hypoplastic anemia","icd10cm","D61.0"
> "1342","congenital hypoplastic anemia","icd10cm","D61.01"
> "1342","congenital hypoplastic anemia","icd9cm","284.0"
> "1342","congenital hypoplastic anemia","mesh","D029502"
> "1342","congenital hypoplastic anemia","umls","C0702159"
> "1342","congenital hypoplastic anemia","umls","C0949116"
> "1342","congenital hypoplastic anemia","mondo","0001713"
> "12668","abnormal retinal correspondence","icd10cm","H53.31"
> "12668","abnormal retinal correspondence","icd9cm","368.34"
> "12668","abnormal retinal correspondence","umls","C0155010"
> "12668","abnormal retinal correspondence","mondo","0001565"
> "0111494","combined oxidative phosphorylation deficiency 4","umls","C1857682"
> "379","external ear disease","icd10cm","H60-H62"
> "379","external ear disease","icd10cm","H61.9"
> "379","external ear disease","icd9cm","380"
> "379","external ear disease","icd9cm","380.9"
> "379","external ear disease","umls","C0155388"
> "379","external ear disease","mondo","0002776"
> "7520","periductal breast myoepitheliosis","umls","C1518974"
> "7520","periductal breast myoepitheliosis","mondo","0004261"
> "7521","breast myoepitheliosis","umls","C1513799"
> "7521","breast myoepitheliosis","mondo","0004262"
> "7527","acute gonococcal endometritis","icd9cm","098.16"
> "7527","acute gonococcal endometritis","umls","C0153196"
> "7527","acute gonococcal endometritis","mondo","0004264"
> "371","extracranial neuroblastoma","umls","C1333499"
> "371","extracranial neuroblastoma","mondo","0002749"
> "7528","acute endometritis","umls","C0238103"
> "7528","acute endometritis","mondo","0004265"
> "374","nutrition disease","mesh","D009748"
> "374","nutrition disease","umls","C3714509"
> "374","nutrition disease","mondo","0005137"
> "0060900","Parkinson's disease 14","mesh","C567844"
> "0060900","Parkinson's disease 14","mondo","0013060"
> "0060901","Waldenstroem's macroglobulinemia","icd10cm","C88.0"
> "0060901","Waldenstroem's macroglobulinemia","icd9cm","273.3"
> "0060901","Waldenstroem's macroglobulinemia","mesh","D008258"
> "0060901","Waldenstroem's macroglobulinemia","umls","C0024419"
> "0060901","Waldenstroem's macroglobulinemia","mondo","0007926"
> "0060902","Norman-Roberts syndrome","mesh","C537848"
> "0060902","Norman-Roberts syndrome","umls","C0796089"
> "0060902","Norman-Roberts syndrome","mondo","0009760"
> "0060903","thrombosis","mesh","D013927"
> "0060903","thrombosis","mondo","0000831"
> "12663","blastomycosis","icd10cm","B40"
> "12663","blastomycosis","icd10cm","B40.9"
> "12663","blastomycosis","icd9cm","116"
> "12663","blastomycosis","icd9cm","116.0"
> "12663","blastomycosis","mesh","D001759"
> "12663","blastomycosis","umls","C0005716"
> "12663","blastomycosis","mondo","0005672"
> "12712","nephronophthisis","icd10cm","Q61.5"
> "12712","nephronophthisis","umls","C0687120"
> "12712","nephronophthisis","mondo","0019005"
> "12711","black piedra","icd10cm","B36.3"
> "12711","black piedra","icd9cm","111.3"
> "12711","black piedra","mesh","D010854"
> "12711","black piedra","umls","C0031898"
> "12711","black piedra","umls","C0153249"
> "12711","black piedra","mondo","0005669"
> "12716","newborn respiratory distress syndrome","icd10cm","P22.0"
> "12716","newborn respiratory distress syndrome","mesh","D006819"
> "12716","newborn respiratory distress syndrome","umls","C0020192"
> "12716","newborn respiratory distress syndrome","mondo","0009971"
> "12714","Ellis-Van Creveld syndrome","icd10cm","Q77.6"
> "12714","Ellis-Van Creveld syndrome","icd9cm","756.55"
> "12714","Ellis-Van Creveld syndrome","mesh","D004613"
> "12714","Ellis-Van Creveld syndrome","umls","C0013903"
> "12714","Ellis-Van Creveld syndrome","mondo","0009162"
> "12718","chronic gonococcal salpingitis","icd9cm","098.37"
> "12718","chronic gonococcal salpingitis","umls","C0153208"
> "12718","chronic gonococcal salpingitis","mondo","0001575"
> "6148","nasal cavity carcinoma in situ","icd10cm","D02.3"
> "6148","nasal cavity carcinoma in situ","umls","C0347095"
> "6148","nasal cavity carcinoma in situ","mondo","0003784"
> "10970","spastic quadriplegia","icd9cm","343.2"
> "10970","spastic quadriplegia","mesh","D002547"
> "10970","spastic quadriplegia","umls","C0154697"
> "10970","spastic quadriplegia","mondo","0016215"
> "10971","acute salpingo-oophoritis","icd10cm","N70.0"
> "10971","acute salpingo-oophoritis","icd10cm","N70.03"
> "10971","acute salpingo-oophoritis","icd9cm","614.0"
> "10971","acute salpingo-oophoritis","umls","C0156327"
> "10971","acute salpingo-oophoritis","mondo","0001171"
> "10972","salpingo-oophoritis","icd10cm","N70"
> "10972","salpingo-oophoritis","icd10cm","N70.9"
> "10972","salpingo-oophoritis","icd10cm","N70.93"
> "10972","salpingo-oophoritis","icd9cm","614.2"
> "10972","salpingo-oophoritis","umls","C0036133"
> "10972","salpingo-oophoritis","mondo","0001172"
> "10973","acute salpingitis","icd10cm","N70.01"
> "10973","acute salpingitis","umls","C0269038"
> "10973","acute salpingitis","mondo","0001173"
> "10974","oophoritis","icd10cm","N70.92"
> "10974","oophoritis","mesh","D009869"
> "10974","oophoritis","umls","C0029051"
> "10974","oophoritis","mondo","0006877"
> "10976","membranous glomerulonephritis","icd10cm","N03.2"
> "10976","membranous glomerulonephritis","mesh","D015433"
> "10976","membranous glomerulonephritis","umls","C0017665"
> "10976","membranous glomerulonephritis","mondo","0005376"
> "0050757","deafness-dystonia-optic neuronopathy syndrome","mesh","C535808"
> "0050757","deafness-dystonia-optic neuronopathy syndrome","mondo","0010578"
> "0050754","ataxia with oculomotor apraxia type 1","mondo","0008842"
> "0050755","ataxia with oculomotor apraxia type 2","mondo","0018996"
> "0050752","amyotrophic lateral sclerosis type 8","mondo","0012077"
> "0050753","cerebellar ataxia","mesh","D002524"
> "0050753","cerebellar ataxia","mondo","0000437"
> "0050759","myotonic dystrophy type 2","icd10cm","G71.1"
> "0050759","myotonic dystrophy type 2","icd10cm","G71.19"
> "0050759","myotonic dystrophy type 2","icd9cm","359.2"
> "0050759","myotonic dystrophy type 2","mesh","D020967"
> "0050759","myotonic dystrophy type 2","umls","C0221055"
> "0050759","myotonic dystrophy type 2","umls","C0553604"
> "0050759","myotonic dystrophy type 2","umls","C0752355"
> "0050759","myotonic dystrophy type 2","mondo","0011266"
> "0050289","fusariosis","mesh","D060585"
> "0050289","fusariosis","mondo","0016426"
> "0111046","platelet-type bleeding disorder 10","mondo","0012031"
> "0111047","platelet-type bleeding disorder 14","mondo","0013597"
> "2277","gonadal disease","mesh","D006058"
> "2277","gonadal disease","umls","C0018050"
> "2277","gonadal disease","mondo","0002259"
> "0111045","platelet-type bleeding disorder 9","icd10cm","D69.8"
> "0111045","platelet-type bleeding disorder 9","mondo","0013622"
> "0111042","glycogen storage disease IXa","icd10cm","E74.0"
> "0111042","glycogen storage disease IXa","mondo","0010598"
> "0111043","glycogen storage disease IXc","icd10cm","E74.0"
> "0111043","glycogen storage disease IXc","mondo","0013091"
> "0111040","glycogen storage disease IXd","icd10cm","E74.0"
> "0111040","glycogen storage disease IXd","mondo","0010362"
> "0111041","glycogen storage disease IXb","icd10cm","E74.0"
> "0111041","glycogen storage disease IXb","mondo","0009868"
> "0111048","platelet-type bleeding disorder 19","icd10cm","D69.4"
> "0111048","platelet-type bleeding disorder 19","mondo","0014518"
> "0111049","platelet-type bleeding disorder 17","icd10cm","D69.1"
> "0111049","platelet-type bleeding disorder 17","mesh","D055652"
> "0111049","platelet-type bleeding disorder 17","umls","C0272302"
> "0111049","platelet-type bleeding disorder 17","mondo","0008553"
> "11595","scleral staphyloma","icd10cm","H15.84"
> "11595","scleral staphyloma","icd9cm","379.11"
> "11595","scleral staphyloma","umls","C0155359"
> "11595","scleral staphyloma","mondo","0001321"
> "11594","ring staphyloma","icd10cm","H15.85"
> "11594","ring staphyloma","icd9cm","379.15"
> "11594","ring staphyloma","umls","C0155363"
> "11594","ring staphyloma","mondo","0001320"
> "11593","bladder lateral wall cancer","icd10cm","C67.2"
> "11593","bladder lateral wall cancer","icd9cm","188.2"
> "11593","bladder lateral wall cancer","umls","C0496828"
> "11593","bladder lateral wall cancer","mondo","0001319"
> "11599","Frey syndrome","mesh","D013547"
> "11599","Frey syndrome","umls","C0038994"
> "11599","Frey syndrome","mondo","0007753"
> "0050133","superficial mycosis","icd10cm","B36.9"
> "0050133","superficial mycosis","mesh","D010854"
> "0050133","superficial mycosis","umls","C0031898"
> "0050133","superficial mycosis","umls","C2980104"
> "0050133","superficial mycosis","mondo","0024268"
> "0050138","podoconiosis","mesh","D004604"
> "0050138","podoconiosis","mondo","0005425"
> "0080328","Culler-Jones syndrome","mondo","0014369"
> "0080326","familial hypertrophic cardiomyopathy","mondo","0024573"
> "0080327","multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly","mondo","0009359"
> "0080324","tuberous sclerosis 1","mondo","0008612"
> "0080325","tuberous sclerosis 2","mondo","0013199"
> "0080322","polycystic kidney disease","mondo","0020642"
> "2051","maxillary sinusitis","icd10cm","J32.0"
> "2051","maxillary sinusitis","mesh","D015523"
> "2051","maxillary sinusitis","umls","C0024959"
> "2051","maxillary sinusitis","mondo","0005842"
> "2050","acute maxillary sinusitis","icd10cm","J01.0"
> "2050","acute maxillary sinusitis","icd10cm","J01.00"
> "2050","acute maxillary sinusitis","icd9cm","461.0"
> "2050","acute maxillary sinusitis","umls","C0155804"
> "2050","acute maxillary sinusitis","mondo","0002186"
> "2053","reactive cutaneous fibrous lesion","umls","C1335666"
> "2053","reactive cutaneous fibrous lesion","mondo","0006603"
> "2055","post-traumatic stress disorder","icd10cm","F43.1"
> "2055","post-traumatic stress disorder","icd10cm","F43.10"
> "2055","post-traumatic stress disorder","icd9cm","309.81"
> "2055","post-traumatic stress disorder","mesh","D013313"
> "2055","post-traumatic stress disorder","umls","C0038436"
> "2055","post-traumatic stress disorder","mondo","0005146"
> "13448","posterior corneal pigmentation","icd10cm","H18.05"
> "13448","posterior corneal pigmentation","icd9cm","371.13"
> "13448","posterior corneal pigmentation","umls","C0155106"
> "13448","posterior corneal pigmentation","mondo","0001717"
> "4829","adenosquamous lung carcinoma","umls","C0279557"
> "4829","adenosquamous lung carcinoma","mondo","0004973"
> "4534","Hallermann-Streiff syndrome","mesh","D006210"
> "4534","Hallermann-Streiff syndrome","umls","C0018522"
> "4534","Hallermann-Streiff syndrome","mondo","0009318"
> "4535","hypotrichosis","mesh","D007039"
> "4535","hypotrichosis","umls","C0020678"
> "4535","hypotrichosis","mondo","0003037"
> "13447","corneal argyrosis","icd10cm","H18.02"
> "13447","corneal argyrosis","icd9cm","371.16"
> "13447","corneal argyrosis","umls","C0155108"
> "13447","corneal argyrosis","mondo","0001716"
> "13446","basilar artery occlusion","icd10cm","I65.1"
> "13446","basilar artery occlusion","icd9cm","433.0"
> "13446","basilar artery occlusion","umls","C0265098"
> "13446","basilar artery occlusion","mondo","0001715"
> "4531","mucoepidermoid carcinoma","mesh","D018277"
> "4531","mucoepidermoid carcinoma","umls","C0206694"
> "4531","mucoepidermoid carcinoma","mondo","0003036"
> "11623","dental pulp necrosis","icd10cm","K04.1"
> "11623","dental pulp necrosis","icd9cm","522.1"
> "11623","dental pulp necrosis","mesh","D003790"
> "11623","dental pulp necrosis","umls","C0011407"
> "11623","dental pulp necrosis","mondo","0001326"
> "9402","epididymitis","icd10cm","N45.1"
> "9402","epididymitis","mesh","D004823"
> "9402","epididymitis","umls","C0014534"
> "9402","epididymitis","mondo","0004779"
> "9401","epididymo-orchitis","icd10cm","N45"
> "9401","epididymo-orchitis","icd10cm","N45.3"
> "9401","epididymo-orchitis","icd9cm","604"
> "9401","epididymo-orchitis","icd9cm","604.90"
> "9401","epididymo-orchitis","umls","C0149881"
> "9401","epididymo-orchitis","mondo","0004778"
> "7983","breast malignant eccrine spiradenoma","umls","C1334565"
> "7983","breast malignant eccrine spiradenoma","mondo","0004420"
> "7984","sclerosing breast papilloma","umls","C1335932"
> "7984","sclerosing breast papilloma","mondo","0004421"
> "9406","hypopituitarism","icd10cm","E23.0"
> "9406","hypopituitarism","mesh","D007018"
> "9406","hypopituitarism","umls","C0020635"
> "9406","hypopituitarism","mondo","0005152"
> "7986","cerebral falx meningioma","umls","C1333597"
> "7986","cerebral falx meningioma","mondo","0004422"
> "11624","penile neoplasm","mesh","D010412"
> "11624","penile neoplasm","umls","C0030849"
> "11624","penile neoplasm","mondo","0006895"
> "9409","diabetes insipidus","icd10cm","E23.2"
> "9409","diabetes insipidus","icd9cm","253.5"
> "9409","diabetes insipidus","mesh","D003919"
> "9409","diabetes insipidus","umls","C0011848"
> "9409","diabetes insipidus","mondo","0004782"
> "9408","acute myocardial infarction","icd10cm","I21"
> "9408","acute myocardial infarction","icd10cm","I21.9"
> "9408","acute myocardial infarction","icd9cm","410"
> "9408","acute myocardial infarction","icd9cm","410.9"
> "9408","acute myocardial infarction","icd9cm","410.90"
> "9408","acute myocardial infarction","umls","C0155626"
> "9408","acute myocardial infarction","mondo","0004781"
> "10627","primary optic atrophy","icd10cm","H47.21"
> "10627","primary optic atrophy","icd9cm","377.11"
> "10627","primary optic atrophy","umls","C0155291"
> "10627","primary optic atrophy","mondo","0001084"
> "14203","childhood type dermatomyositis","icd10cm","M33.0"
> "14203","childhood type dermatomyositis","mesh","D003882"
> "14203","childhood type dermatomyositis","umls","C0263666"
> "14203","childhood type dermatomyositis","mondo","0008054"
> "11971","synostosis","mesh","D013580"
> "11971","synostosis","umls","C0039093"
> "11971","synostosis","mondo","0001411"
> "11976","botulism","icd10cm","A05.1"
> "11976","botulism","mesh","D001906"
> "11976","botulism","umls","C0006057"
> "11976","botulism","mondo","0005498"
> "11975","coloboma of optic nerve","icd10cm","H47.31"
> "11975","coloboma of optic nerve","icd10cm","H47.319"
> "11975","coloboma of optic nerve","icd10cm","Q14.2"
> "11975","coloboma of optic nerve","icd9cm","377.23"
> "11975","coloboma of optic nerve","mesh","C535970"
> "11975","coloboma of optic nerve","umls","C0155299"
> "11975","coloboma of optic nerve","mondo","0007354"
> "13198","endemic goiter","icd10cm","E01.0"
> "13198","endemic goiter","icd10cm","E01.2"
> "13198","endemic goiter","icd9cm","240.0"
> "13198","endemic goiter","mesh","D006043"
> "13198","endemic goiter","umls","C0018022"
> "13198","endemic goiter","mondo","0006742"
> "13197","nodular goiter","mesh","D006044"
> "13197","nodular goiter","umls","C0018023"
> "13197","nodular goiter","mondo","0006869"
> "13196","lingual goiter","mesh","D047268"
> "13196","lingual goiter","umls","C0271760"
> "13196","lingual goiter","mondo","0006833"
> "13195","nontoxic goiter","icd10cm","E04.0"
> "13195","nontoxic goiter","icd10cm","E04.9"
> "13195","nontoxic goiter","umls","C0221777"
> "13195","nontoxic goiter","mondo","0001658"
> "0110795","hereditary spastic paraplegia 43","icd10cm","G11.4"
> "0110795","hereditary spastic paraplegia 43","mondo","0014024"
> "0110794","hereditary spastic paraplegia 42","icd10cm","G11.4"
> "0110794","hereditary spastic paraplegia 42","mondo","0012928"
> "0110797","hereditary spastic paraplegia 45","icd10cm","G11.4"
> "0110797","hereditary spastic paraplegia 45","mondo","0013165"
> "0110796","hereditary spastic paraplegia 44","icd10cm","G11.4"
> "0110796","hereditary spastic paraplegia 44","mondo","0013179"
> "0110791","hereditary spastic paraplegia 3A","icd10cm","G11.4"
> "0110791","hereditary spastic paraplegia 3A","mondo","0008437"
> "0110790","hereditary spastic paraplegia 39","icd10cm","G11.4"
> "0110790","hereditary spastic paraplegia 39","mondo","0012787"
> "0110793","hereditary spastic paraplegia 41","icd10cm","G11.4"
> "0110793","hereditary spastic paraplegia 41","mondo","0013239"
> "0110792","hereditary spastic paraplegia 4","icd10cm","G11.4"
> "0110792","hereditary spastic paraplegia 4","mondo","0008438"
> "0110799","hereditary spastic paraplegia 47","mondo","0013551"
> "0110798","hereditary spastic paraplegia 46","icd10cm","G11.4"
> "0110798","hereditary spastic paraplegia 46","mondo","0013737"
> "2097","vulval Paget's disease","umls","C1275217"
> "2097","vulval Paget's disease","mondo","0002207"
> "12803","Sly syndrome","icd10cm","E76.29"
> "12803","Sly syndrome","mesh","D016538"
> "12803","Sly syndrome","umls","C0085132"
> "12803","Sly syndrome","mondo","0009662"
> "0070264","congenital disorder of glycosylation type IIl","mondo","0013810"
> "0070265","congenital disorder of glycosylation type IIm","mondo","0010478"
> "0070266","congenital disorder of glycosylation type IIn","mondo","0014746"
> "0070267","congenital disorder of glycosylation type IIo","mondo","0014789"
> "0070260","congenital disorder of glycosylation type IIh","umls","C1970021"
> "0070260","congenital disorder of glycosylation type IIh","mondo","0012635"
> "0070261","congenital disorder of glycosylation type IIi","mondo","0013325"
> "0070262","congenital disorder of glycosylation type IIj","mondo","0013281"
> "0070263","congenital disorder of glycosylation type IIk","mondo","0013870"
> "10087","gastric leiomyoma","umls","C0238440"
> "10087","gastric leiomyoma","mondo","0000938"
> "0070268","congenital disorder of glycosylation type IIp","mondo","0014790"
> "0070269","congenital disorder of glycosylation type IIq","mondo","0054559"
> "0110571","autosomal dominant nonsyndromic deafness 48","icd10cm","H90.3"
> "0110571","autosomal dominant nonsyndromic deafness 48","mondo","0011920"
> "0110570","autosomal dominant nonsyndromic deafness 47","icd10cm","H90.3"
> "0110570","autosomal dominant nonsyndromic deafness 47","mondo","0012090"
> "0110573","autosomal dominant nonsyndromic deafness 4A","icd10cm","H90.3"
> "0110573","autosomal dominant nonsyndromic deafness 4A","mondo","0010915"
> "0110572","autosomal dominant nonsyndromic deafness 49","icd10cm","H90.3"
> "0110572","autosomal dominant nonsyndromic deafness 49","mondo","0012023"
> "0110575","autosomal dominant nonsyndromic deafness 5","icd10cm","H90.3"
> "0110575","autosomal dominant nonsyndromic deafness 5","mondo","0010973"
> "0110574","autosomal dominant nonsyndromic deafness 4B","icd10cm","H90.3"
> "0110574","autosomal dominant nonsyndromic deafness 4B","mondo","0013823"
> "0110577","autosomal dominant nonsyndromic deafness 51","icd10cm","H90.3"
> "0110577","autosomal dominant nonsyndromic deafness 51","mondo","0013305"
> "0110576","autosomal dominant nonsyndromic deafness 50","icd10cm","H90.3"
> "0110576","autosomal dominant nonsyndromic deafness 50","mondo","0013114"
> "0110579","autosomal dominant nonsyndromic deafness 53","icd10cm","H90.3"
> "0110579","autosomal dominant nonsyndromic deafness 53","mondo","0012380"
> "0110578","autosomal dominant nonsyndromic deafness 52","icd10cm","H90.3"
> "0110578","autosomal dominant nonsyndromic deafness 52","mondo","0011893"
> "12958","paralytic lagophthalmos","icd10cm","H02.23"
> "12958","paralytic lagophthalmos","icd9cm","374.21"
> "12958","paralytic lagophthalmos","umls","C0155197"
> "12958","paralytic lagophthalmos","mondo","0001603"
> "12959","lagophthalmos","icd10cm","H02.2"
> "12959","lagophthalmos","icd10cm","H02.20"
> "12959","lagophthalmos","icd9cm","374.2"
> "12959","lagophthalmos","icd9cm","374.20"
> "12959","lagophthalmos","umls","C0152226"
> "12959","lagophthalmos","mondo","0001604"
> "0060333","mitochondrial complex V (ATP synthase) deficiency nuclear type 4","icd10cm","E88.8"
> "0060333","mitochondrial complex V (ATP synthase) deficiency nuclear type 4","mondo","0014091"
> "0060332","mitochondrial complex V (ATP synthase) deficiency nuclear type 3","icd10cm","E88.8"
> "0060332","mitochondrial complex V (ATP synthase) deficiency nuclear type 3","mondo","0013547"
> "0060331","mitochondrial complex V (ATP synthase) deficiency nuclear type 2","icd10cm","G71.3"
> "0060331","mitochondrial complex V (ATP synthase) deficiency nuclear type 2","mondo","0013546"
> "0060330","Rapp-Hodgkin syndrome","mesh","C535289"
> "0060330","Rapp-Hodgkin syndrome","mondo","0007508"
> "0060337","CEDNIK syndrome","mesh","C537943"
> "0060337","CEDNIK syndrome","umls","C1836033"
> "0060337","CEDNIK syndrome","mondo","0012290"
> "0060336","3-methylglutaconic aciduria","icd10cm","E71.111"
> "0060336","3-methylglutaconic aciduria","mesh","C579867"
> "0060336","3-methylglutaconic aciduria","mondo","0017359"
> "0060335","autosomal dominant sideroblastic anemia 4","mondo","0008422"
> "0060334","transient neonatal diabetes mellitus","icd10cm","P70.2"
> "0060334","transient neonatal diabetes mellitus","mondo","0020525"
> "8857","lupus erythematosus","icd10cm","L93"
> "8857","lupus erythematosus","icd10cm","L93.0"
> "8857","lupus erythematosus","icd9cm","695.4"
> "8857","lupus erythematosus","umls","C0409974"
> "8857","lupus erythematosus","mondo","0004670"
> "0060339","chronic atrial and intestinal dysrhythmia","mondo","0014528"
> "7061","precursor B lymphoblastic lymphoma/leukemia","umls","C0862030"
> "7061","precursor B lymphoblastic lymphoma/leukemia","mondo","0004947"
> "11685","inflamed seborrheic keratosis","icd10cm","L82.0"
> "11685","inflamed seborrheic keratosis","icd9cm","702.11"
> "11685","inflamed seborrheic keratosis","umls","C0376117"
> "11685","inflamed seborrheic keratosis","mondo","0001337"
> "11684","melanoacanthoma","umls","C1321683"
> "11684","melanoacanthoma","mondo","0006579"
> "10400","gonococcal seminal vesiculitis","umls","C0578661"
> "10400","gonococcal seminal vesiculitis","mondo","0001027"
> "6961","Bartholin's gland squamous cell carcinoma","umls","C1511052"
> "6961","Bartholin's gland squamous cell carcinoma","mondo","0004053"
> "8628","Hodgkin's lymphoma, lymphocytic depletion","icd10cm","C81.3"
> "8628","Hodgkin's lymphoma, lymphocytic depletion","icd9cm","201.7"
> "8628","Hodgkin's lymphoma, lymphocytic depletion","mesh","D006689"
> "8628","Hodgkin's lymphoma, lymphocytic depletion","umls","C0152267"
> "8628","Hodgkin's lymphoma, lymphocytic depletion","mondo","0004620"
> "8158","complement component 5 deficiency","mondo","0012295"
> "6969","acute canaliculitis","icd10cm","H04.33"
> "6969","acute canaliculitis","icd9cm","375.31"
> "6969","acute canaliculitis","umls","C0339130"
> "6969","acute canaliculitis","mondo","0004054"
> "8153","fibroosseous pseudotumor of digits","umls","C1333612"
> "8153","fibroosseous pseudotumor of digits","mondo","0004482"
> "8150","pancreatic invasive intraductal papillary-mucinous carcinoma","umls","C1518871"
> "8150","pancreatic invasive intraductal papillary-mucinous carcinoma","mondo","0004481"
> "8151","appendiceal L-cell glucagon-like peptide producing tumor","umls","C3274138"
> "8151","appendiceal L-cell glucagon-like peptide producing tumor","mondo","0021101"
> "0060488","Pitt-Hopkins syndrome","mesh","C537403"
> "0060488","Pitt-Hopkins syndrome","umls","C1970431"
> "0060488","Pitt-Hopkins syndrome","mondo","0012589"
> "0060485","Mowat-Wilson syndrome","mesh","C536990"
> "0060485","Mowat-Wilson syndrome","umls","C1856113"
> "0060485","Mowat-Wilson syndrome","mondo","0009341"
> "0060484","EAST syndrome","mesh","C557674"
> "0060484","EAST syndrome","umls","C2748572"
> "0060484","EAST syndrome","mondo","0013005"
> "0060486","Perry syndrome","mesh","C566822"
> "0060486","Perry syndrome","mondo","0008201"
> "0060481","Goldberg-Shprintzen syndrome","mesh","C537279"
> "0060481","Goldberg-Shprintzen syndrome","umls","C1836123"
> "0060481","Goldberg-Shprintzen syndrome","mondo","0012280"
> "0060480","left ventricular noncompaction","mondo","0018901"
> "0060483","MEDNIK syndrome","mondo","0012251"
> "0060482","oculoauricular syndrome","icd10cm","Q87.8"
> "0060482","oculoauricular syndrome","mesh","C567416"
> "0060482","oculoauricular syndrome","mondo","0012802"
> "9988","tertiary neurosyphilis","icd10cm","A52.3"
> "9988","tertiary neurosyphilis","icd9cm","094"
> "9988","tertiary neurosyphilis","icd9cm","094.9"
> "9988","tertiary neurosyphilis","mesh","D009494"
> "9988","tertiary neurosyphilis","umls","C0027927"
> "9988","tertiary neurosyphilis","mondo","0004944"
> "9986","orbit lymphoma","mesh","C537131"
> "9986","orbit lymphoma","umls","C0271333"
> "9986","orbit lymphoma","mondo","0004942"
> "9987","orbit sarcoma","umls","C1335131"
> "9987","orbit sarcoma","mondo","0004943"
> "14504","Niemann-Pick disease","icd10cm","E75.24"
> "14504","Niemann-Pick disease","icd10cm","E75.249"
> "14504","Niemann-Pick disease","mesh","D009542"
> "14504","Niemann-Pick disease","umls","C0028064"
> "14504","Niemann-Pick disease","mondo","0001982"
> "14507","peripheral degeneration of cornea","icd10cm","H18.46"
> "14507","peripheral degeneration of cornea","icd9cm","371.48"
> "14507","peripheral degeneration of cornea","umls","C0155123"
> "14507","peripheral degeneration of cornea","mondo","0001983"
> "14501","Sjogren-Larsson syndrome","mesh","D016111"
> "14501","Sjogren-Larsson syndrome","umls","C0037231"
> "14501","Sjogren-Larsson syndrome","mondo","0010031"
> "14500","fucosidosis","icd10cm","E77.1"
> "14500","fucosidosis","mesh","D005645"
> "14500","fucosidosis","umls","C0016788"
> "14500","fucosidosis","mondo","0009254"
> "14503","neuronal ceroid lipofuscinosis","icd10cm","E75.4"
> "14503","neuronal ceroid lipofuscinosis","mesh","D009472"
> "14503","neuronal ceroid lipofuscinosis","umls","C0027877"
> "14503","neuronal ceroid lipofuscinosis","mondo","0016295"
> "14502","cholesterol ester storage disease","mesh","D015217"
> "14502","cholesterol ester storage disease","umls","C0008384"
> "14502","cholesterol ester storage disease","mondo","0019149"
> "11029","pinguecula","icd10cm","H11.15"
> "11029","pinguecula","icd9cm","372.51"
> "11029","pinguecula","mesh","D059407"
> "11029","pinguecula","umls","C0152255"
> "11029","pinguecula","mondo","0001179"
> "11028","pseudopterygium","icd9cm","372.52"
> "11028","pseudopterygium","umls","C0155161"
> "11028","pseudopterygium","mondo","0001178"
> "417","autoimmune hypersensitivity disease","icd9cm","720"
> "417","autoimmune hypersensitivity disease","umls","C0003089"
> "417","autoimmune hypersensitivity disease","mondo","0007179"
> "1388","Tangier disease","icd10cm","E78.6"
> "1388","Tangier disease","mesh","D013631"
> "1388","Tangier disease","umls","C0039292"
> "1388","Tangier disease","mondo","0008783"
> "1389","polyneuropathy","icd10cm","A69.22"
> "1389","polyneuropathy","icd10cm","G62.9"
> "1389","polyneuropathy","mesh","D011115"
> "1389","polyneuropathy","umls","C0152025"
> "1389","polyneuropathy","mondo","0001824"
> "1386","abetalipoproteinemia","icd10cm","E78.6"
> "1386","abetalipoproteinemia","mesh","D000012"
> "1386","abetalipoproteinemia","umls","C0000744"
> "1386","abetalipoproteinemia","mondo","0008692"
> "1387","hypolipoproteinemia","icd10cm","E78.6"
> "1387","hypolipoproteinemia","icd9cm","272.5"
> "1387","hypolipoproteinemia","mesh","D007009"
> "1387","hypolipoproteinemia","umls","C0020623"
> "1387","hypolipoproteinemia","mondo","0001822"
> "1380","endometrial cancer","kegg","05213"
> "1380","endometrial cancer","icd10cm","C54.1"
> "1380","endometrial cancer","mesh","D016889"
> "1380","endometrial cancer","umls","C0007103"
> "1380","endometrial cancer","umls","C0014170"
> "1380","endometrial cancer","mondo","0011962"
> "419","scleroderma","mesh","D012594"
> "419","scleroderma","umls","C0011644"
> "419","scleroderma","mondo","0019340"
> "1382","miliaria","icd10cm","L74.3"
> "1382","miliaria","mesh","D008883"
> "1382","miliaria","umls","C0026113"
> "1382","miliaria","mondo","0006580"
> "1383","sweat gland disease","icd10cm","L74"
> "1383","sweat gland disease","icd10cm","L74.9"
> "1383","sweat gland disease","icd9cm","705"
> "1383","sweat gland disease","icd9cm","705.9"
> "1383","sweat gland disease","mesh","D013543"
> "1383","sweat gland disease","umls","C0038986"
> "1383","sweat gland disease","mondo","0006615"
> "11367","congenital aphakia","icd10cm","Q12.3"
> "11367","congenital aphakia","icd9cm","743.35"
> "11367","congenital aphakia","umls","C0152422"
> "11367","congenital aphakia","mondo","0012456"
> "11364","lens subluxation","icd10cm","H27.11"
> "11364","lens subluxation","icd9cm","379.32"
> "11364","lens subluxation","mesh","D007906"
> "11364","lens subluxation","umls","C0023316"
> "11364","lens subluxation","mondo","0001271"
> "11360","Phlebotomus fever","icd10cm","A93.1"
> "11360","Phlebotomus fever","icd9cm","066.0"
> "11360","Phlebotomus fever","mesh","D010217"
> "11360","Phlebotomus fever","umls","C0030372"
> "11360","Phlebotomus fever","mondo","0005913"
> "1777","unilateral hyperactive labyrinth","icd9cm","386.51"
> "1777","unilateral hyperactive labyrinth","umls","C0155515"
> "1777","unilateral hyperactive labyrinth","mondo","0002107"
> "1770","toxic megacolon","icd10cm","K59.31"
> "1770","toxic megacolon","mesh","D008532"
> "1770","toxic megacolon","umls","C0025162"
> "1770","toxic megacolon","mondo","0002105"
> "6688","autoimmune lymphoproliferative syndrome","icd10cm","D89.82"
> "6688","autoimmune lymphoproliferative syndrome","icd9cm","279.41"
> "6688","autoimmune lymphoproliferative syndrome","mesh","D056735"
> "6688","autoimmune lymphoproliferative syndrome","umls","C1328840"
> "6688","autoimmune lymphoproliferative syndrome","mondo","0017979"
> "6680","Capgras syndrome","mesh","D002194"
> "6680","Capgras syndrome","umls","C0006895"
> "6680","Capgras syndrome","mondo","0003965"
> "6682","spondylolisthesis","icd10cm","M43.1"
> "6682","spondylolisthesis","icd10cm","M43.10"
> "6682","spondylolisthesis","mesh","D013168"
> "6682","spondylolisthesis","umls","C0038016"
> "6682","spondylolisthesis","mondo","0008475"
> "6683","Aarskog syndrome","icd10cm","Q87.1"
> "6683","Aarskog syndrome","mesh","C535331"
> "6683","Aarskog syndrome","umls","C0175701"
> "6683","Aarskog syndrome","mondo","0007030"
> "6686","Achard syndrome","mesh","C536012"
> "6686","Achard syndrome","umls","C1332135"
> "6686","Achard syndrome","mondo","0007036"
> "6687","Achenbach syndrome","umls","C0473563"
> "6687","Achenbach syndrome","mondo","0006520"
> "0110885","inflammatory bowel disease 10","mondo","0012610"
> "0110884","inflammatory bowel disease 23","mondo","0012887"
> "0110887","inflammatory bowel disease 12","mondo","0012829"
> "2426","gangliocytoma","mesh","D005729"
> "2426","gangliocytoma","mondo","0016730"
> "0070079","schizophrenia 3","mondo","0010897"
> "0070078","schizophrenia 2","mondo","0011307"
> "0110886","inflammatory bowel disease 9","mondo","0012040"
> "7849","dendritic cell sarcoma","umls","C1301364"
> "7849","dendritic cell sarcoma","mondo","0004380"
> "7848","interdigitating dendritic cell sarcoma","icd10cm","C96.4"
> "7848","interdigitating dendritic cell sarcoma","mesh","D054739"
> "7848","interdigitating dendritic cell sarcoma","umls","C1260326"
> "7848","interdigitating dendritic cell sarcoma","mondo","0005813"
> "0070071","autosomal dominant non-syndromic intellectual disability 41","mondo","0014842"
> "0070070","autosomal dominant non-syndromic intellectual disability 40","mondo","0014699"
> "0070073","autosomal dominant non-syndromic intellectual disability 43","mondo","0014858"
> "0070072","autosomal dominant non-syndromic intellectual disability 42","mondo","0014855"
> "7841","pediatric cerebral ependymoblastoma","umls","C1332962"
> "7841","pediatric cerebral ependymoblastoma","mondo","0004378"
> "7840","pancreatic non-functioning delta cell tumor","umls","C1335311"
> "7840","pancreatic non-functioning delta cell tumor","mondo","0004377"
> "7843","female breast carcinoma","umls","C0007104"
> "7843","female breast carcinoma","mondo","0004379"
> "0110880","holoprosencephaly 4","mondo","0007734"
> "6354","CLL/SLL","umls","C1302547"
> "6354","CLL/SLL","mondo","0003864"
> "0110883","inflammatory bowel disease 17","mondo","0012840"
> "0110882","inflammatory bowel disease 7","mondo","0011521"
> "12108","bullous retinoschisis","icd9cm","361.12"
> "12108","bullous retinoschisis","umls","C0344289"
> "12108","bullous retinoschisis","mondo","0001435"
> "9617","orthostatic proteinuria","icd10cm","R80.2"
> "9617","orthostatic proteinuria","icd9cm","593.6"
> "9617","orthostatic proteinuria","umls","C0232867"
> "9617","orthostatic proteinuria","mondo","0004838"
> "9346","Taylor's syndrome","icd9cm","625.5"
> "9346","Taylor's syndrome","umls","C0152078"
> "9346","Taylor's syndrome","mondo","0004762"
> "9348","carotid artery dissection","icd10cm","I77.71"
> "9348","carotid artery dissection","icd9cm","443.21"
> "9348","carotid artery dissection","umls","C0338585"
> "9348","carotid artery dissection","mondo","0004763"
> "1811","reflex sympathetic dystrophy","icd10cm","G90.5"
> "1811","reflex sympathetic dystrophy","icd10cm","M89.0"
> "1811","reflex sympathetic dystrophy","icd9cm","337.2"
> "1811","reflex sympathetic dystrophy","icd9cm","337.20"
> "1811","reflex sympathetic dystrophy","icd9cm","337.21"
> "1811","reflex sympathetic dystrophy","mesh","D012019"
> "1811","reflex sympathetic dystrophy","umls","C0034931"
> "1811","reflex sympathetic dystrophy","mondo","0011441"
> "14080","glucocorticoid-remediable aldosteronism","icd10cm","E26.02"
> "14080","glucocorticoid-remediable aldosteronism","icd9cm","255.11"
> "14080","glucocorticoid-remediable aldosteronism","mesh","C563177"
> "14080","glucocorticoid-remediable aldosteronism","umls","C1260386"
> "14080","glucocorticoid-remediable aldosteronism","mondo","0007080"
> "14081","toxic labyrinthitis","icd9cm","386.34"
> "14081","toxic labyrinthitis","umls","C0155507"
> "14081","toxic labyrinthitis","mondo","0001874"
> "14087","epicondylitis","icd10cm","M77.1"
> "14087","epicondylitis","icd9cm","726.32"
> "14087","epicondylitis","mesh","D013716"
> "14087","epicondylitis","umls","C0014488"
> "14087","epicondylitis","umls","C0039516"
> "14087","epicondylitis","mondo","0001875"
> "14089","root caries","icd9cm","521.08"
> "14089","root caries","mesh","D017213"
> "14089","root caries","umls","C0162644"
> "14089","root caries","mondo","0006957"
> "3229","gastric dilatation","mesh","D013271"
> "3229","gastric dilatation","umls","C0038353"
> "3229","gastric dilatation","mondo","0002569"
> "1979","focal chorioretinitis","icd10cm","H30.0"
> "1979","focal chorioretinitis","icd10cm","H30.00"
> "1979","focal chorioretinitis","icd9cm","363.0"
> "1979","focal chorioretinitis","icd9cm","363.00"
> "1979","focal chorioretinitis","umls","C0154870"
> "1979","focal chorioretinitis","mondo","0002164"
> "3225","tracheal disease","icd10cm","S12.8"
> "3225","tracheal disease","mesh","D014133"
> "3225","tracheal disease","umls","C0040580"
> "3225","tracheal disease","mondo","0002567"
> "3227","tracheal stenosis","mesh","D014135"
> "3227","tracheal stenosis","umls","C0040583"
> "3227","tracheal stenosis","mondo","0002568"
> "1602","lymphadenitis","icd10cm","I88.1"
> "1602","lymphadenitis","icd10cm","I88.9"
> "1602","lymphadenitis","icd10cm","L04"
> "1602","lymphadenitis","icd10cm","L04.9"
> "1602","lymphadenitis","icd9cm","289.1"
> "1602","lymphadenitis","icd9cm","683"
> "1602","lymphadenitis","mesh","D008199"
> "1602","lymphadenitis","umls","C0024205"
> "1602","lymphadenitis","umls","C0154304"
> "1602","lymphadenitis","umls","C0157705"
> "1602","lymphadenitis","mondo","0002052"
2247,2248c7517,7522
< "1970","fallopian tube carcinosarcoma","umls","C1517117"
< "1970","fallopian tube carcinosarcoma","mondo","0006207"
---
> "3223","complex regional pain syndrome","mesh","D020918"
> "3223","complex regional pain syndrome","umls","C0458219"
> "3223","complex regional pain syndrome","mondo","0019369"
> "3222","causalgia","mesh","D002422"
> "3222","causalgia","umls","C0007462"
> "3222","causalgia","mondo","0020572"
2252a7527,7533
> "13711","dental fluorosis","icd10cm","K00.3"
> "13711","dental fluorosis","icd9cm","520.3"
> "13711","dental fluorosis","mesh","D009050"
> "13711","dental fluorosis","umls","C0026618"
> "13711","dental fluorosis","mondo","0006722"
> "0111567","retinal vasculopathy with cerebral leukodystrophy","mesh","C566007"
> "0111567","retinal vasculopathy with cerebral leukodystrophy","umls","C1860518"
2257,2276c7538,7548
< "0110568","autosomal dominant nonsyndromic deafness 43","icd10cm","H90.3"
< "0110568","autosomal dominant nonsyndromic deafness 43","mondo","0012030"
< "0110569","autosomal dominant nonsyndromic deafness 44","icd10cm","H90.3"
< "0110569","autosomal dominant nonsyndromic deafness 44","mondo","0011832"
< "0110566","autosomal dominant nonsyndromic deafness 40","icd10cm","H90.3"
< "0110566","autosomal dominant nonsyndromic deafness 40","mondo","0014603"
< "0110567","autosomal dominant nonsyndromic deafness 41","icd10cm","H90.3"
< "0110567","autosomal dominant nonsyndromic deafness 41","mondo","0011994"
< "0110564","autosomal dominant nonsyndromic deafness 3A","icd10cm","H90.3"
< "0110564","autosomal dominant nonsyndromic deafness 3A","mondo","0011103"
< "0110565","autosomal dominant nonsyndromic deafness 3B","icd10cm","H90.3"
< "0110565","autosomal dominant nonsyndromic deafness 3B","mondo","0012975"
< "0110562","autosomal dominant nonsyndromic deafness 33","icd10cm","H90.3"
< "0110562","autosomal dominant nonsyndromic deafness 33","mondo","0013632"
< "0110563","autosomal dominant nonsyndromic deafness 36","icd10cm","H90.3"
< "0110563","autosomal dominant nonsyndromic deafness 36","mondo","0011708"
< "0110560","autosomal dominant nonsyndromic deafness 30","icd10cm","H90.3"
< "0110560","autosomal dominant nonsyndromic deafness 30","mondo","0011673"
< "0110561","autosomal dominant nonsyndromic deafness 31","icd10cm","H90.3"
< "0110561","autosomal dominant nonsyndromic deafness 31","mondo","0012086"
---
> "13270","erythropoietic protoporphyria","icd10cm","E80.0"
> "13270","erythropoietic protoporphyria","mesh","D046351"
> "13270","erythropoietic protoporphyria","umls","C0162568"
> "13270","erythropoietic protoporphyria","mondo","0001676"
> "13271","cutaneous porphyria","icd10cm","E80.0"
> "13271","cutaneous porphyria","mesh","D017092"
> "13271","cutaneous porphyria","umls","C0162530"
> "13271","cutaneous porphyria","mondo","0009902"
> "0111569","autosomal dominant vitreoretinochoroidopathy","mesh","C536352"
> "0111569","autosomal dominant vitreoretinochoroidopathy","umls","C3888099"
> "0111568","congenital vertical talus","umls","C0240912"
2289,2299c7561,7580
< "0110212","Charcot-Marie-Tooth disease X-linked recessive 4","icd10cm","G60.0"
< "0110212","Charcot-Marie-Tooth disease X-linked recessive 4","mondo","0010689"
< "2616","Wolffian duct adenoma","umls","C0334530"
< "2616","Wolffian duct adenoma","mondo","0002364"
< "12929","endocardial fibroelastosis","icd10cm","I42.4"
< "12929","endocardial fibroelastosis","icd9cm","425.3"
< "12929","endocardial fibroelastosis","mesh","D004695"
< "12929","endocardial fibroelastosis","umls","C0014117"
< "12929","endocardial fibroelastosis","mondo","0009169"
< "0110218","Brugada syndrome 1","icd10cm","I49.8"
< "0110218","Brugada syndrome 1","mondo","0011001"
---
> "2848","melancholia","mesh","D003866"
> "2848","melancholia","umls","C0025193"
> "2848","melancholia","mondo","0002444"
> "0110213","isolated cleft palate","icd10cm","Q35.1"
> "0110213","isolated cleft palate","icd10cm","Q35.3"
> "0110213","isolated cleft palate","icd10cm","Q35.5"
> "0110213","isolated cleft palate","icd10cm","Q35.7"
> "0110213","isolated cleft palate","icd10cm","Q35.9"
> "0110213","isolated cleft palate","mondo","0007336"
> "2846","bruxism","icd10cm","F45.8"
> "2846","bruxism","icd10cm","G47.63"
> "2846","bruxism","icd9cm","327.53"
> "2846","bruxism","mesh","D002012"
> "2846","bruxism","mesh","D020186"
> "2846","bruxism","umls","C0006325"
> "2846","bruxism","umls","C0393774"
> "2846","bruxism","mondo","0002443"
> "2842","Jervell-Lange Nielsen syndrome","mesh","D029593"
> "2842","Jervell-Lange Nielsen syndrome","umls","C0022387"
> "2842","Jervell-Lange Nielsen syndrome","mondo","0002441"
2307,2310c7588,7598
< "12294","atypical depressive disorder","icd10cm","F32.89"
< "12294","atypical depressive disorder","icd9cm","296.82"
< "12294","atypical depressive disorder","umls","C0154437"
< "12294","atypical depressive disorder","mondo","0001485"
---
> "2841","asthma","kegg","05310"
> "2841","asthma","icd10cm","J45"
> "2841","asthma","icd10cm","J45.90"
> "2841","asthma","icd10cm","J45.909"
> "2841","asthma","icd9cm","493"
> "2841","asthma","icd9cm","493.9"
> "2841","asthma","mesh","D001249"
> "2841","asthma","umls","C0004096"
> "2841","asthma","mondo","0004979"
> "5476","cervical adenofibroma","umls","C1516402"
> "5476","cervical adenofibroma","mondo","0003459"
2314,2317c7602,7603
< "3322","GM1 gangliosidosis","icd10cm","E75.19"
< "3322","GM1 gangliosidosis","mesh","D016537"
< "3322","GM1 gangliosidosis","umls","C0085131"
< "3322","GM1 gangliosidosis","mondo","0018149"
---
> "5474","ovarian serous adenofibroma","umls","C1518729"
> "5474","ovarian serous adenofibroma","mondo","0006340"
2327,2332c7613,7628
< "14264","benign neonatal seizures","mesh","D020936"
< "14264","benign neonatal seizures","umls","C0270851"
< "14264","benign neonatal seizures","mondo","0016027"
< "14265","pulmonary valve insufficiency","mesh","D011665"
< "14265","pulmonary valve insufficiency","umls","C0034088"
< "14265","pulmonary valve insufficiency","mondo","0001927"
---
> "3325","hyperglobulinemic purpura","mesh","D011694"
> "3325","hyperglobulinemic purpura","umls","C0034151"
> "3325","hyperglobulinemic purpura","mondo","0006792"
> "3326","purpura","icd10cm","D69.2"
> "3326","purpura","mesh","D011693"
> "3326","purpura","umls","C0034150"
> "3326","purpura","mondo","0002610"
> "3327","partial motor epilepsy","mesh","D020938"
> "3327","partial motor epilepsy","umls","C0016399"
> "3327","partial motor epilepsy","mondo","0006891"
> "3328","temporal lobe epilepsy","mesh","D004833"
> "3328","temporal lobe epilepsy","umls","C0014556"
> "3328","temporal lobe epilepsy","mondo","0005115"
> "3329","benign epilepsy with centrotemporal spikes","mesh","D019305"
> "3329","benign epilepsy with centrotemporal spikes","umls","C0376532"
> "3329","benign epilepsy with centrotemporal spikes","mondo","0007295"
2338,2343c7634,7635
< "14262","oral candidiasis","icd10cm","B37.0"
< "14262","oral candidiasis","icd10cm","B37.9"
< "14262","oral candidiasis","icd9cm","112.0"
< "14262","oral candidiasis","mesh","D002180"
< "14262","oral candidiasis","umls","C0006849"
< "14262","oral candidiasis","mondo","0005886"
---
> "5478","fallopian tube adenofibroma","umls","C1517109"
> "5478","fallopian tube adenofibroma","mondo","0003461"
2346,2431d7637
< "10184","spindle cell lipoma","umls","C0334474"
< "10184","spindle cell lipoma","mondo","0000962"
< "9478","postpartum depression","icd10cm","F53"
< "9478","postpartum depression","mesh","D019052"
< "9478","postpartum depression","umls","C0221074"
< "9478","postpartum depression","mondo","0005929"
< "5271","small intestine leiomyosarcoma","umls","C0920305"
< "5271","small intestine leiomyosarcoma","mondo","0003360"
< "5272","small intestinal sarcoma","umls","C1336007"
< "5272","small intestinal sarcoma","mondo","0003361"
< "0060327","omphalocele","icd10cm","Q79.2"
< "0060327","omphalocele","icd9cm","756.72"
< "0060327","omphalocele","mesh","D006554"
< "0060327","omphalocele","umls","C0795690"
< "0060327","omphalocele","umls","C1306503"
< "0060327","omphalocele","mondo","0019015"
< "0060329","ectopic pregnancy","icd10cm","O00"
< "0060329","ectopic pregnancy","icd10cm","O00.9"
< "0060329","ectopic pregnancy","icd10cm","O00.90"
< "0060329","ectopic pregnancy","icd9cm","633"
< "0060329","ectopic pregnancy","icd9cm","633.9"
< "0060329","ectopic pregnancy","mesh","D011271"
< "0060329","ectopic pregnancy","umls","C0032987"
< "0060329","ectopic pregnancy","mondo","0000755"
< "0111015","Newfoundland cone-rod dystrophy","mondo","0011839"
< "10188","skin lipoma","icd9cm","214.0"
< "10188","skin lipoma","umls","C0153968"
< "10188","skin lipoma","umls","C0347394"
< "10188","skin lipoma","umls","C1333174"
< "10188","skin lipoma","mondo","0000964"
< "4757","testicular sex cord-stromal neoplasm","umls","C1515289"
< "4757","testicular sex cord-stromal neoplasm","mondo","0003125"
< "0040099","livedoid vasculitis","icd10cm","L95.0"
< "0040099","livedoid vasculitis","icd9cm","709.1"
< "0040099","livedoid vasculitis","mondo","0025514"
< "0040093","drug-induced lupus erythematosus","icd10cm","M32.0"
< "0040093","drug-induced lupus erythematosus","umls","C0263591"
< "0040093","drug-induced lupus erythematosus","mondo","0016474"
< "9111","cutaneous leishmaniasis","icd10cm","B55.1"
< "9111","cutaneous leishmaniasis","mesh","D016773"
< "9111","cutaneous leishmaniasis","umls","C0023283"
< "9111","cutaneous leishmaniasis","mondo","0005446"
< "2999","granulosa cell tumor","mesh","D006106"
< "2999","granulosa cell tumor","umls","C0018206"
< "2999","granulosa cell tumor","umls","C0334401"
< "2999","granulosa cell tumor","mondo","0006036"
< "8634","prostate carcinoma in situ","icd10cm","D07.5"
< "8634","prostate carcinoma in situ","icd9cm","233.4"
< "8634","prostate carcinoma in situ","umls","C0154088"
< "8634","prostate carcinoma in situ","mondo","0004623"
< "8632","Kaposi's sarcoma","icd10cm","C46"
< "8632","Kaposi's sarcoma","icd10cm","C46.0"
< "8632","Kaposi's sarcoma","icd10cm","C46.1"
< "8632","Kaposi's sarcoma","icd10cm","C46.2"
< "8632","Kaposi's sarcoma","icd10cm","C46.3"
< "8632","Kaposi's sarcoma","icd10cm","C46.4"
< "8632","Kaposi's sarcoma","icd10cm","C46.5"
< "8632","Kaposi's sarcoma","icd10cm","C46.9"
< "8632","Kaposi's sarcoma","icd9cm","176"
< "8632","Kaposi's sarcoma","icd9cm","176.0"
< "8632","Kaposi's sarcoma","icd9cm","176.1"
< "8632","Kaposi's sarcoma","icd9cm","176.2"
< "8632","Kaposi's sarcoma","icd9cm","176.3"
< "8632","Kaposi's sarcoma","icd9cm","176.4"
< "8632","Kaposi's sarcoma","icd9cm","176.5"
< "8632","Kaposi's sarcoma","icd9cm","176.9"
< "8632","Kaposi's sarcoma","mesh","D012514"
< "8632","Kaposi's sarcoma","umls","C0036220"
< "8632","Kaposi's sarcoma","umls","C0153560"
< "8632","Kaposi's sarcoma","umls","C0153561"
< "8632","Kaposi's sarcoma","umls","C0153562"
< "8632","Kaposi's sarcoma","umls","C0153563"
< "8632","Kaposi's sarcoma","umls","C0153564"
< "8632","Kaposi's sarcoma","umls","C0153565"
< "8632","Kaposi's sarcoma","umls","C0346935"
< "8632","Kaposi's sarcoma","umls","C0346936"
< "8632","Kaposi's sarcoma","umls","C1332265"
< "8632","Kaposi's sarcoma","umls","C1332847"
< "8632","Kaposi's sarcoma","umls","C1333453"
< "8632","Kaposi's sarcoma","umls","C1333744"
< "8632","Kaposi's sarcoma","umls","C1333776"
< "8632","Kaposi's sarcoma","umls","C1334318"
< "8632","Kaposi's sarcoma","umls","C1334457"
< "8632","Kaposi's sarcoma","umls","C1335372"
< "8632","Kaposi's sarcoma","umls","C1335509"
< "8632","Kaposi's sarcoma","mondo","0005055"
2437,2438d7642
< "4938","ureter adenocarcinoma","umls","C1336873"
< "4938","ureter adenocarcinoma","mondo","0003216"
2440a7645,7646
> "5510","pineal dysgerminoma","umls","C1335415"
> "5510","pineal dysgerminoma","mondo","0003480"
2453,2505c7659,7660
< "2998","testicular cancer","icd10cm","C62"
< "2998","testicular cancer","icd10cm","C62.9"
< "2998","testicular cancer","icd10cm","C62.90"
< "2998","testicular cancer","icd9cm","186"
< "2998","testicular cancer","mesh","D013736"
< "2998","testicular cancer","umls","C0039590"
< "2998","testicular cancer","umls","C0153594"
< "2998","testicular cancer","umls","C1333010"
< "2998","testicular cancer","mondo","0005447"
< "0110496","autosomal recessive nonsyndromic deafness 38","icd10cm","H90.3"
< "0110496","autosomal recessive nonsyndromic deafness 38","mondo","0011991"
< "3039","cecum adenocarcinoma","umls","C1332866"
< "3039","cecum adenocarcinoma","mondo","0006028"
< "1557","hypersensitivity reaction type III disease","mesh","D007105"
< "1557","hypersensitivity reaction type III disease","umls","C0020951"
< "1557","hypersensitivity reaction type III disease","mondo","0007004"
< "0110497","autosomal recessive nonsyndromic deafness 39","icd10cm","H90.3"
< "0110497","autosomal recessive nonsyndromic deafness 39","mondo","0012003"
< "11102","bartonellosis","icd10cm","A44"
< "11102","bartonellosis","icd10cm","A44.9"
< "11102","bartonellosis","icd9cm","088.0"
< "11102","bartonellosis","mesh","D001474"
< "11102","bartonellosis","umls","C0004771"
< "11102","bartonellosis","mondo","0005664"
< "11103","rickettsialpox","icd10cm","A79.1"
< "11103","rickettsialpox","icd9cm","083.2"
< "11103","rickettsialpox","mesh","D000073605"
< "11103","rickettsialpox","umls","C0035597"
< "11103","rickettsialpox","mondo","0019360"
< "11100","Q fever","icd10cm","A78"
< "11100","Q fever","icd9cm","083.0"
< "11100","Q fever","mesh","D011778"
< "11100","Q fever","umls","C0034362"
< "11100","Q fever","mondo","0019186"
< "0060491","SPOAN syndrome","icd10cm","G11.4"
< "0060491","SPOAN syndrome","mesh","C563702"
< "0060491","SPOAN syndrome","mondo","0012297"
< "2994","germ cell cancer","mesh","D009373"
< "2994","germ cell cancer","umls","C0205851"
< "2994","germ cell cancer","mondo","0005040"
< "0060888","transient myeloproliferative syndrome","icd10cm","D47.7"
< "0060888","transient myeloproliferative syndrome","mondo","0008040"
< "11104","spotted fever","icd10cm","A77"
< "11104","spotted fever","icd10cm","A77.9"
< "11104","spotted fever","icd9cm","082.0"
< "11104","spotted fever","mesh","D000073605"
< "11104","spotted fever","umls","C0038041"
< "11104","spotted fever","mondo","0001195"
< "11105","fundus albipunctatus","icd10cm","H35.52"
< "11105","fundus albipunctatus","icd9cm","362.74"
< "11105","fundus albipunctatus","mesh","C562733"
< "11105","fundus albipunctatus","umls","C0311338"
< "11105","fundus albipunctatus","mondo","0007639"
---
> "7347","ovarian stromal hyperthecosis","umls","C1518743"
> "7347","ovarian stromal hyperthecosis","mondo","0004194"
2509,2512c7664,7686
< "0060258","reticulate acropigmentation of Kitamura","mesh","C562924"
< "0060258","reticulate acropigmentation of Kitamura","umls","C0406811"
< "0060258","reticulate acropigmentation of Kitamura","mondo","0014234"
< "0060259","renal-hepatic-pancreatic dysplasia","mondo","0017417"
---
> "533","thymus gland disease","icd10cm","E32"
> "533","thymus gland disease","icd10cm","E32.9"
> "533","thymus gland disease","icd9cm","254"
> "533","thymus gland disease","icd9cm","254.9"
> "533","thymus gland disease","umls","C0154199"
> "533","thymus gland disease","mondo","0003393"
> "530","eyelid disease","icd10cm","H02.9"
> "530","eyelid disease","icd9cm","374.9"
> "530","eyelid disease","mesh","D005141"
> "530","eyelid disease","umls","C0015423"
> "530","eyelid disease","mondo","0003382"
> "539","ophthalmoplegia","icd9cm","378.56"
> "539","ophthalmoplegia","mesh","D009886"
> "539","ophthalmoplegia","umls","C0029089"
> "539","ophthalmoplegia","umls","C0155338"
> "539","ophthalmoplegia","mondo","0003425"
> "538","internuclear ophthalmoplegia","icd10cm","H51.2"
> "538","internuclear ophthalmoplegia","icd9cm","378.86"
> "538","internuclear ophthalmoplegia","mesh","D015835"
> "538","internuclear ophthalmoplegia","umls","C0152134"
> "538","internuclear ophthalmoplegia","mondo","0003417"
> "0070204","familial partial lipodystrophy type 3","umls","C1720861"
> "0070204","familial partial lipodystrophy type 3","mondo","0011448"
2517,2603c7691,7704
< "0060254","Robinow syndrome","mesh","C562492"
< "0060254","Robinow syndrome","umls","C0265205"
< "0060254","Robinow syndrome","mondo","0019978"
< "0110492","autosomal recessive nonsyndromic deafness 33","icd10cm","H90.3"
< "0110492","autosomal recessive nonsyndromic deafness 33","mondo","0011799"
< "0060256","Dowling-Degos disease","mesh","C562924"
< "0060256","Dowling-Degos disease","umls","C0406811"
< "0060256","Dowling-Degos disease","umls","C3714534"
< "0060256","Dowling-Degos disease","mondo","0008371"
< "0060257","dyschromatosis symmetrica hereditaria","mesh","C535729"
< "0060257","dyschromatosis symmetrica hereditaria","umls","C0406775"
< "0060257","dyschromatosis symmetrica hereditaria","mondo","0007483"
< "0060490","Schimke immuno-osseous dysplasia","mesh","C536629"
< "0060490","Schimke immuno-osseous dysplasia","umls","C0877024"
< "0060490","Schimke immuno-osseous dysplasia","mondo","0009458"
< "0060252","sclerocornea","mesh","C565209"
< "0060252","sclerocornea","umls","C1853235"
< "0060252","sclerocornea","mondo","0019629"
< "0050634","alopecia universalis","mondo","0008757"
< "9113","granuloma inguinale","icd10cm","A58"
< "9113","granuloma inguinale","icd9cm","099.2"
< "9113","granuloma inguinale","mesh","D006100"
< "9113","granuloma inguinale","umls","C0018190"
< "9113","granuloma inguinale","mondo","0005777"
< "0060475","childhood onset epileptic encephalopathy","mondo","0014150"
< "0060476","Perlman syndrome","icd10cm","Q87.3"
< "0060476","Perlman syndrome","mesh","C536399"
< "0060476","Perlman syndrome","mondo","0009965"
< "11101","trench fever","icd10cm","A79.0"
< "11101","trench fever","icd9cm","083.1"
< "11101","trench fever","mesh","D014205"
< "11101","trench fever","umls","C0040830"
< "11101","trench fever","mondo","0005991"
< "0060470","salt and pepper syndrome","mondo","0018275"
< "0060471","fetal valproate syndrome","mesh","C536525"
< "0060471","fetal valproate syndrome","umls","C0236026"
< "0060471","fetal valproate syndrome","mondo","0012275"
< "0060472","Kindler syndrome","mesh","C536321"
< "0060472","Kindler syndrome","mondo","0008260"
< "0060473","Kabuki syndrome","mesh","C537705"
< "0060473","Kabuki syndrome","umls","C0796004"
< "0060473","Kabuki syndrome","mondo","0016512"
< "3030","mucinous adenocarcinoma","mesh","D002288"
< "3030","mucinous adenocarcinoma","umls","C0007130"
< "3030","mucinous adenocarcinoma","umls","C0334368"
< "3030","mucinous adenocarcinoma","mondo","0004957"
< "0070205","familial partial lipodystrophy type 4","mondo","0013478"
< "0060478","Zika fever","icd10cm","A92.8"
< "0060478","Zika fever","mesh","D000071243"
< "0060478","Zika fever","mondo","0018661"
< "0060479","Shwachman-Diamond syndrome","icd10cm","D61.0"
< "0060479","Shwachman-Diamond syndrome","mesh","C537330"
< "0060479","Shwachman-Diamond syndrome","mondo","0009833"
< "12859","choreatic disease","icd10cm","G25.5"
< "12859","choreatic disease","mondo","0001595"
< "12858","Huntington's disease","kegg","05016"
< "12858","Huntington's disease","icd10cm","G10"
< "12858","Huntington's disease","icd9cm","333.4"
< "12858","Huntington's disease","mesh","D006816"
< "12858","Huntington's disease","umls","C0020179"
< "12858","Huntington's disease","mondo","0007739"
< "0090130","cortical dysplasia-focal epilepsy syndrome","icd10cm","Q04.8"
< "0090130","cortical dysplasia-focal epilepsy syndrome","mondo","0012400"
< "53","pituitary gland disease","icd9cm","253.1"
< "53","pituitary gland disease","umls","C0029493"
< "53","pituitary gland disease","mondo","0003381"
< "5136","lung leiomyoma","umls","C1334447"
< "5136","lung leiomyoma","mondo","0003293"
< "12583","velocardiofacial syndrome","icd10cm","Q93.81"
< "12583","velocardiofacial syndrome","icd9cm","758.32"
< "12583","velocardiofacial syndrome","mesh","D004062"
< "12583","velocardiofacial syndrome","umls","C0220704"
< "12583","velocardiofacial syndrome","mondo","0008644"
< "205","hyperostosis","icd10cm","M89.3"
< "205","hyperostosis","icd10cm","M89.30"
< "205","hyperostosis","mesh","D015576"
< "205","hyperostosis","umls","C0020492"
< "205","hyperostosis","mondo","0002185"
< "9993","hypoglycemia","icd10cm","E16.2"
< "9993","hypoglycemia","icd9cm","251.2"
< "9993","hypoglycemia","mesh","D007003"
< "9993","hypoglycemia","umls","C0020615"
< "9993","hypoglycemia","mondo","0004946"
< "8527","monocytic leukemia","icd10cm","C93"
< "8527","monocytic leukemia","icd9cm","206.8"
< "8527","monocytic leukemia","umls","C0153903"
< "8527","monocytic leukemia","mondo","0004600"
---
> "1909","melanoma","kegg","05218"
> "1909","melanoma","mesh","D008545"
> "1909","melanoma","umls","C0025202"
> "1909","melanoma","mondo","0005105"
> "1906","malignant skin fibrous histiocytoma","umls","C1275254"
> "1906","malignant skin fibrous histiocytoma","mondo","0002141"
> "14464","neuroleptic malignant syndrome","icd10cm","G21.0"
> "14464","neuroleptic malignant syndrome","icd9cm","333.92"
> "14464","neuroleptic malignant syndrome","mesh","D009459"
> "14464","neuroleptic malignant syndrome","umls","C0027849"
> "14464","neuroleptic malignant syndrome","mondo","0019790"
> "1907","malignant fibroxanthoma","mesh","D051677"
> "1907","malignant fibroxanthoma","umls","C0334463"
> "1907","malignant fibroxanthoma","mondo","0002142"
2612,2659c7713,7738
< "0060787","hypomyelinating leukodystrophy 2","icd10cm","E75.2"
< "0060787","hypomyelinating leukodystrophy 2","mondo","0012125"
< "0060784","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","mesh","C536189"
< "0060784","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","umls","C0406704"
< "0060784","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","mondo","0007520"
< "14515","WAGR syndrome","mesh","D017624"
< "14515","WAGR syndrome","umls","C0206115"
< "14515","WAGR syndrome","mondo","0008681"
< "0060782","EEC syndrome","mesh","C536189"
< "0060782","EEC syndrome","umls","C0406704"
< "0060782","EEC syndrome","mondo","0010004"
< "0060783","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","mesh","C536189"
< "0060783","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","umls","C0406704"
< "0060783","ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","mondo","0011428"
< "0060780","congenital diarrhea 6","icd10cm","P78.3"
< "0060780","congenital diarrhea 6","mondo","0013825"
< "0060781","congenital secretory sodium diarrhea 3","icd10cm","P78.3"
< "0060781","congenital secretory sodium diarrhea 3","mondo","0010036"
< "0060877","bullous congenital ichthyosiform erythroderma","mesh","D053560"
< "0060877","bullous congenital ichthyosiform erythroderma","umls","C0432306"
< "0060877","bullous congenital ichthyosiform erythroderma","mondo","0007813"
< "0060788","hypomyelinating leukodystrophy 10","mondo","0014632"
< "0060789","hypomyelinating leukodystrophy 4","icd10cm","E75.2"
< "0060789","hypomyelinating leukodystrophy 4","mondo","0012824"
< "0060878","hypoparathyroidism-deafness-renal disease syndrome","mesh","C537907"
< "0060878","hypoparathyroidism-deafness-renal disease syndrome","umls","C1840333"
< "0060878","hypoparathyroidism-deafness-renal disease syndrome","mondo","0007797"
< "6193","epithelioid sarcoma","umls","C0205944"
< "6193","epithelioid sarcoma","mondo","0017387"
< "1398","parasitic infectious disease","icd10cm","H44.12"
< "1398","parasitic infectious disease","icd9cm","360.13"
< "1398","parasitic infectious disease","umls","C0014238"
< "1398","parasitic infectious disease","mondo","0005135"
< "10021","duodenum cancer","icd10cm","C17.0"
< "10021","duodenum cancer","icd9cm","152.0"
< "10021","duodenum cancer","mesh","D004379"
< "10021","duodenum cancer","umls","C0153426"
< "10021","duodenum cancer","umls","C0541912"
< "10021","duodenum cancer","mondo","0000920"
< "0050246","granulomatous amebic encephalitis","mondo","0000291"
< "1390","hypobetalipoproteinemia","mesh","D006995"
< "1390","hypobetalipoproteinemia","umls","C0020597"
< "1390","hypobetalipoproteinemia","mondo","0017774"
< "8941","seborrheic infantile dermatitis","icd10cm","L21.0"
< "8941","seborrheic infantile dermatitis","icd9cm","690.11"
< "8941","seborrheic infantile dermatitis","mesh","D063807"
< "8941","seborrheic infantile dermatitis","umls","C0221244"
< "8941","seborrheic infantile dermatitis","mondo","0006609"
---
> "6510","lung occult squamous cell carcinoma","umls","C1335100"
> "6510","lung occult squamous cell carcinoma","mondo","0003904"
> "6511","glandular pattern ovarian yolk sac tumor","umls","C1518747"
> "6511","glandular pattern ovarian yolk sac tumor","mondo","0003905"
> "6512","hepatoid pattern ovarian yolk sac tumor","umls","C1518748"
> "6512","hepatoid pattern ovarian yolk sac tumor","mondo","0003906"
> "6514","polyvesicular vitelline pattern ovarian yolk sac tumor","umls","C1518749"
> "6514","polyvesicular vitelline pattern ovarian yolk sac tumor","mondo","0003907"
> "6517","clivus meningioma","umls","C1333073"
> "6517","clivus meningioma","mondo","0003908"
> "10792","chronic maxillary sinusitis","icd10cm","J32.0"
> "10792","chronic maxillary sinusitis","icd9cm","473.0"
> "10792","chronic maxillary sinusitis","umls","C0008698"
> "10792","chronic maxillary sinusitis","mondo","0001122"
> "0080064","autosomal recessive spinocerebellar ataxia 17","mondo","0014503"
> "10793","chronic sphenoidal sinusitis","icd10cm","J32.3"
> "10793","chronic sphenoidal sinusitis","icd9cm","473.3"
> "10793","chronic sphenoidal sinusitis","umls","C0008712"
> "10793","chronic sphenoidal sinusitis","mondo","0001123"
> "3813","central nervous system chondroma","umls","C1333019"
> "3813","central nervous system chondroma","mondo","0002779"
> "3816","glossopharyngeal nerve paralysis","umls","C0919940"
> "3816","glossopharyngeal nerve paralysis","mondo","0002781"
> "3817","cranial nerve palsy","mesh","D003389"
> "3817","cranial nerve palsy","umls","C0151311"
> "3817","cranial nerve palsy","mondo","0002782"
2663,2669c7742,7744
< "8704","genital herpes","icd9cm","054.1"
< "8704","genital herpes","icd9cm","054.10"
< "8704","genital herpes","mesh","D006558"
< "8704","genital herpes","umls","C0019342"
< "8704","genital herpes","mondo","0005770"
< "3450","cutaneous Paget's disease","mesh","D010145"
< "3450","cutaneous Paget's disease","mondo","0002655"
---
> "3819","toxicodendron dermatitis","mesh","D011040"
> "3819","toxicodendron dermatitis","umls","C0032342"
> "3819","toxicodendron dermatitis","mondo","0006616"
2682,2710c7757,7770
< "3451","skin carcinoma","umls","C0699893"
< "3451","skin carcinoma","mondo","0002656"
< "13317","hyperinsulinemic hypoglycemia","icd10cm","E16.9"
< "13317","hyperinsulinemic hypoglycemia","mesh","D046768"
< "13317","hyperinsulinemic hypoglycemia","umls","C0027773"
< "13317","hyperinsulinemic hypoglycemia","mondo","0005803"
< "3606","ovarian mucinous adenocarcinoma","umls","C1335167"
< "3606","ovarian mucinous adenocarcinoma","mondo","0005601"
< "0080181","PHARC syndrome","mondo","0012984"
< "3456","cervix erosion","mesh","D002579"
< "3456","cervix erosion","umls","C0007869"
< "3456","cervix erosion","mondo","0006696"
< "11656","cicatricial pemphigoid","icd10cm","L12.1"
< "11656","cicatricial pemphigoid","icd9cm","694.6"
< "11656","cicatricial pemphigoid","icd9cm","694.61"
< "11656","cicatricial pemphigoid","mesh","D010390"
< "11656","cicatricial pemphigoid","umls","C0030804"
< "11656","cicatricial pemphigoid","umls","C0157721"
< "11656","cicatricial pemphigoid","mondo","0018746"
< "851","Bartholin's duct cyst","icd10cm","N75.0"
< "851","Bartholin's duct cyst","icd9cm","616.2"
< "851","Bartholin's duct cyst","umls","C0004767"
< "851","Bartholin's duct cyst","mondo","0004593"
< "12148","alveolar echinococcosis","icd10cm","B67.6"
< "12148","alveolar echinococcosis","icd10cm","B67.7"
< "12148","alveolar echinococcosis","icd9cm","122.7"
< "12148","alveolar echinococcosis","mesh","C536591"
< "12148","alveolar echinococcosis","umls","C0152069"
< "12148","alveolar echinococcosis","mondo","0017282"
---
> "8454","ariboflavinosis","icd10cm","E53.0"
> "8454","ariboflavinosis","icd9cm","266.0"
> "8454","ariboflavinosis","mesh","D012257"
> "8454","ariboflavinosis","umls","C0035528"
> "8454","ariboflavinosis","mondo","0004573"
> "0080063","autosomal recessive spinocerebellar ataxia 11","mondo","0013645"
> "0060672","Grn-related frontotemporal lobar degeneration with Tdp43 inclusions","icd10cm","G31.0"
> "0060672","Grn-related frontotemporal lobar degeneration with Tdp43 inclusions","mondo","0011842"
> "7549","ceruminoma","umls","C0334352"
> "7549","ceruminoma","mondo","0004276"
> "0060670","cerebral cavernous malformation 2","icd10cm","Q28.3"
> "0060670","cerebral cavernous malformation 2","mondo","0011304"
> "0060671","cerebral cavernous malformation 3","icd10cm","Q28.3"
> "0060671","cerebral cavernous malformation 3","mondo","0011305"
2715,2720c7775,7776
< "162","cancer","icd10cm","C80"
< "162","cancer","icd10cm","C80.1"
< "162","cancer","icd9cm","199"
< "162","cancer","mesh","D009369"
< "162","cancer","umls","C0006826"
< "162","cancer","mondo","0004992"
---
> "0060674","catecholaminergic polymorphic ventricular tachycardia","icd10cm","I47.2"
> "0060674","catecholaminergic polymorphic ventricular tachycardia","mondo","0017990"
2723,2724c7779,7784
< "0060678","catecholaminergic polymorphic ventricular tachycardia 4","icd10cm","I47.2"
< "0060678","catecholaminergic polymorphic ventricular tachycardia 4","mondo","0013966"
---
> "7540","breast apocrine adenoma","umls","C1388299"
> "7540","breast apocrine adenoma","mondo","0004273"
> "7541","mixed epithelial/mesenchymal metaplastic breast carcinoma","umls","C1513365"
> "7541","mixed epithelial/mesenchymal metaplastic breast carcinoma","mondo","0004274"
> "7542","osteosarcoma arising in bone Paget's disease","umls","C1335148"
> "7542","osteosarcoma arising in bone Paget's disease","mondo","0004275"
2727,2754c7787,7788
< "3458","breast adenocarcinoma","umls","C0858252"
< "3458","breast adenocarcinoma","mondo","0004988"
< "0060474","familial erythrocytosis 2","icd10cm","D75.1"
< "0060474","familial erythrocytosis 2","mondo","0009892"
< "0060871","autosomal dominant keratitis-ichthyosis-deafness syndrome","icd10cm","Q80.8"
< "0060871","autosomal dominant keratitis-ichthyosis-deafness syndrome","mondo","0007850"
< "0110086","asphyxiating thoracic dystrophy 2","icd10cm","Q77.2"
< "0110086","asphyxiating thoracic dystrophy 2","mondo","0012644"
< "0060394","chromosome 15q13.3 microdeletion syndrome","icd10cm","Q93.5"
< "0060394","chromosome 15q13.3 microdeletion syndrome","mesh","C567439"
< "0060394","chromosome 15q13.3 microdeletion syndrome","mondo","0012774"
< "0110080","Leber congenital amaurosis 12","icd10cm","H35.5"
< "0110080","Leber congenital amaurosis 12","mondo","0012525"
< "0110962","brachydactyly-preaxial hallux varus syndrome","icd10cm","Q73.8"
< "0110962","brachydactyly-preaxial hallux varus syndrome","mondo","0007214"
< "0110963","Ballard syndrome","icd10cm","Q73.8"
< "0110963","Ballard syndrome","mondo","0007213"
< "0110960","Gaucher's disease perinatal lethal","icd10cm","E75.2"
< "0110960","Gaucher's disease perinatal lethal","mondo","0011945"
< "8036","childhood ovarian embryonal carcinoma","umls","C1332989"
< "8036","childhood ovarian embryonal carcinoma","mondo","0004441"
< "0110966","brachydactyly type A3","mondo","0007217"
< "0110967","brachydactyly type A4","icd10cm","Q73.8"
< "0110967","brachydactyly type A4","mondo","0007218"
< "0110964","brachydactyly type A1","mondo","0007215"
< "0110965","brachydactyly type A2","mesh","C537089"
< "0110965","brachydactyly type A2","umls","C1832702"
< "0110965","brachydactyly type A2","mondo","0007216"
---
> "6161","childhood testicular mixed germ cell tumor","umls","C1333009"
> "6161","childhood testicular mixed germ cell tumor","mondo","0003787"
2757,2765c7791,7806
< "0110968","brachydactyly type A6","mesh","C537092"
< "0110968","brachydactyly type A6","umls","C1862130"
< "0110968","brachydactyly type A6","mondo","0007219"
< "0110969","brachydactyly type B1","mondo","0007220"
< "0060872","isolated growth hormone deficiency type II","icd10cm","E23.0"
< "0060872","isolated growth hormone deficiency type II","mondo","0008250"
< "14749","methylmalonic acidemia","mondo","0002012"
< "0050788","proximal symphalangism","kegg","H00484"
< "0050788","proximal symphalangism","mondo","0008511"
---
> "6163","familial renal papillary carcinoma","umls","C0879257"
> "6163","familial renal papillary carcinoma","mondo","0003789"
> "6162","childhood embryonal testis carcinoma","umls","C1333007"
> "6162","childhood embryonal testis carcinoma","mondo","0003788"
> "12735","hernia of ovary and fallopian tube","icd10cm","N83.4"
> "12735","hernia of ovary and fallopian tube","icd10cm","N83.40"
> "12735","hernia of ovary and fallopian tube","icd9cm","620.4"
> "12735","hernia of ovary and fallopian tube","umls","C0495094"
> "12735","hernia of ovary and fallopian tube","mondo","0001578"
> "6167","prostatic urethral cancer","umls","C1514523"
> "6167","prostatic urethral cancer","mondo","0003791"
> "6166","prostatic urethra urothelial carcinoma","umls","C1514522"
> "6166","prostatic urethra urothelial carcinoma","mondo","0003790"
> "10997","immature cataract","icd10cm","H25.09"
> "10997","immature cataract","umls","C0271163"
> "10997","immature cataract","mondo","0001175"
2769,2776c7810,7813
< "0060392","chromosome 14q11-q22 deletion syndrome","mondo","0013272"
< "0060816","corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome","icd10cm","Q87.8"
< "0060816","corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome","mondo","0010333"
< "0060817","syndromic X-linked intellectual disability 34","mondo","0010501"
< "0060814","Wilson-Turner syndrome","mondo","0010665"
< "0060815","Miles-Carpenter syndrome","mesh","C537472"
< "0060815","Miles-Carpenter syndrome","umls","C1839735"
< "0060815","Miles-Carpenter syndrome","mondo","0010666"
---
> "10991","basal ganglia cerebrovascular disease","mesh","D020144"
> "10991","basal ganglia cerebrovascular disease","umls","C0751739"
> "10991","basal ganglia cerebrovascular disease","mondo","0006505"
> "0050730","coenzyme Q10 deficiency disease","mondo","0018151"
2778,2783d7814
< "0060813","syndromic X-linked intellectual disability Shrimpton type","icd10cm","Q87.8"
< "0060813","syndromic X-linked intellectual disability Shrimpton type","mondo","0010409"
< "0060810","syndromic X-linked intellectual disability type 10","icd10cm","G25.5"
< "0060810","syndromic X-linked intellectual disability type 10","mondo","0010272"
< "0060811","syndromic X-linked intellectual disability Turner type","icd10cm","Q87.8"
< "0060811","syndromic X-linked intellectual disability Turner type","mondo","0010407"
2789,2832c7820,7845
< "0060818","syndromic X-linked intellectual disability Abidi type","mesh","C535556"
< "0060818","syndromic X-linked intellectual disability Abidi type","umls","C1846056"
< "0060818","syndromic X-linked intellectual disability Abidi type","mondo","0010285"
< "0060819","syndromic X-linked intellectual disability Chudley-Schwartz type","mondo","0010462"
< "8252","chronic rhinitis","icd10cm","J31.0"
< "8252","chronic rhinitis","icd9cm","472.0"
< "8252","chronic rhinitis","umls","C0008711"
< "8252","chronic rhinitis","mondo","0004514"
< "0111009","cone-rod dystrophy 1","mondo","0010905"
< "4606","bile duct cancer","icd10cm","C24.0"
< "4606","bile duct cancer","icd9cm","156.1"
< "4606","bile duct cancer","mesh","D001650"
< "4606","bile duct cancer","umls","C0005396"
< "4606","bile duct cancer","umls","C0153453"
< "4606","bile duct cancer","mondo","0003059"
< "4607","biliary tract cancer","icd10cm","C24.9"
< "4607","biliary tract cancer","icd9cm","156.9"
< "4607","biliary tract cancer","mesh","D001661"
< "4607","biliary tract cancer","umls","C0005426"
< "4607","biliary tract cancer","umls","C0750952"
< "4607","biliary tract cancer","mondo","0003060"
< "13515","tuberous sclerosis","icd10cm","Q85.1"
< "13515","tuberous sclerosis","icd9cm","759.5"
< "13515","tuberous sclerosis","mesh","D014402"
< "13515","tuberous sclerosis","umls","C0041341"
< "13515","tuberous sclerosis","mondo","0001734"
< "224","transient cerebral ischemia","icd10cm","G45.9"
< "224","transient cerebral ischemia","mesh","D002546"
< "224","transient cerebral ischemia","umls","C0007787"
< "224","transient cerebral ischemia","mondo","0005264"
< "12028","Conn's syndrome","icd10cm","E26.0"
< "12028","Conn's syndrome","icd10cm","E26.01"
< "12028","Conn's syndrome","icd9cm","255.12"
< "12028","Conn's syndrome","mesh","D006929"
< "12028","Conn's syndrome","umls","C1384514"
< "12028","Conn's syndrome","mondo","0001422"
< "222","perichondritis of auricle","icd10cm","H61.0"
< "222","perichondritis of auricle","icd10cm","H61.00"
< "222","perichondritis of auricle","icd10cm","H61.009"
< "222","perichondritis of auricle","icd9cm","380.0"
< "222","perichondritis of auricle","icd9cm","380.00"
< "222","perichondritis of auricle","umls","C0155389"
< "222","perichondritis of auricle","mondo","0002246"
< "0111020","cone-rod dystrophy 9","mondo","0013002"
---
> "0080128","mitochondrial DNA depletion syndrome 9","mesh","C580473"
> "0080128","mitochondrial DNA depletion syndrome 9","mondo","0009504"
> "0080129","mitochondrial DNA depletion syndrome 11","mondo","0014039"
> "0080124","mitochondrial DNA depletion syndrome 5","mesh","C567624"
> "0080124","mitochondrial DNA depletion syndrome 5","mesh","C580473"
> "0080124","mitochondrial DNA depletion syndrome 5","mondo","0012791"
> "0080125","mitochondrial DNA depletion syndrome 6","mesh","C538344"
> "0080125","mitochondrial DNA depletion syndrome 6","mondo","0009747"
> "0080126","mitochondrial DNA depletion syndrome 7","mesh","C535523"
> "0080126","mitochondrial DNA depletion syndrome 7","mondo","0010060"
> "0080127","mitochondrial DNA depletion syndrome 8a","mesh","C536350"
> "0080127","mitochondrial DNA depletion syndrome 8a","mondo","0012792"
> "0080120","mitochondrial DNA depletion syndrome 2","mesh","C563698"
> "0080120","mitochondrial DNA depletion syndrome 2","mondo","0012301"
> "0080121","mitochondrial DNA depletion syndrome 3","mesh","C580039"
> "0080121","mitochondrial DNA depletion syndrome 3","mondo","0009636"
> "0080122","mitochondrial DNA depletion syndrome 4a","icd10cm","G31.81"
> "0080122","mitochondrial DNA depletion syndrome 4a","mesh","D002549"
> "0080122","mitochondrial DNA depletion syndrome 4a","umls","C0205710"
> "0080122","mitochondrial DNA depletion syndrome 4a","mondo","0008758"
> "0080123","mitochondrial DNA depletion syndrome 4b","mondo","0013350"
> "2213","hemorrhagic disease","icd10cm","D69.9"
> "2213","hemorrhagic disease","icd9cm","287.9"
> "2213","hemorrhagic disease","mesh","D006474"
> "2213","hemorrhagic disease","umls","C0019087"
> "2213","hemorrhagic disease","mondo","0002243"
2839,2841c7852,7862
< "0111025","cone-rod dystrophy 19","mondo","0014372"
< "0111026","cone-rod dystrophy 20","mondo","0014427"
< "0111027","hemochromatosis type 2A","mondo","0011216"
---
> "2216","factor V deficiency","icd10cm","D68.2"
> "2216","factor V deficiency","mesh","D005166"
> "2216","factor V deficiency","umls","C0015499"
> "2216","factor V deficiency","mondo","0009210"
> "2215","factor VII deficiency","icd10cm","D68.2"
> "2215","factor VII deficiency","mesh","D005168"
> "2215","factor VII deficiency","umls","C0015503"
> "2215","factor VII deficiency","mondo","0009211"
> "2214","inherited blood coagulation disease","mesh","D025861"
> "2214","inherited blood coagulation disease","umls","C0852077"
> "2214","inherited blood coagulation disease","mondo","0021181"
2851,2894c7872,7875
< "0110936","nemaline myopathy 5","mondo","0011539"
< "5475","uterine corpus adenofibroma","umls","C1336901"
< "5475","uterine corpus adenofibroma","mondo","0003458"
< "2338","mandibular cancer","icd10cm","C41.1"
< "2338","mandibular cancer","icd9cm","170.1"
< "2338","mandibular cancer","mesh","D008339"
< "2338","mandibular cancer","umls","C0024694"
< "2338","mandibular cancer","umls","C0153511"
< "2338","mandibular cancer","mondo","0005837"
< "2339","Crouzon syndrome","icd10cm","Q75.1"
< "2339","Crouzon syndrome","mesh","D003394"
< "2339","Crouzon syndrome","umls","C0010273"
< "2339","Crouzon syndrome","mondo","0007405"
< "6692","Barre-Lieou syndrome","icd10cm","M53.0"
< "6692","Barre-Lieou syndrome","mesh","D055010"
< "6692","Barre-Lieou syndrome","umls","C0376378"
< "6692","Barre-Lieou syndrome","mondo","0005663"
< "734","urethra cancer","icd10cm","C68.0"
< "734","urethra cancer","icd9cm","189.3"
< "734","urethra cancer","mesh","D014523"
< "734","urethra cancer","umls","C0153620"
< "734","urethra cancer","umls","C0700101"
< "734","urethra cancer","mondo","0004192"
< "0110716","Warburg micro syndrome 1","icd10cm","Q87.0"
< "0110716","Warburg micro syndrome 1","mondo","0010822"
< "0070066","autosomal dominant non-syndromic intellectual disability 36","mondo","0014605"
< "0070067","White-Sutton syndrome","mondo","0014606"
< "0070064","autosomal dominant non-syndromic intellectual disability 34","mondo","0014599"
< "0070065","autosomal dominant non-syndromic intellectual disability 35","mondo","0014602"
< "0070062","autosomal dominant non-syndromic intellectual disability 32","mondo","0014558"
< "0070063","autosomal dominant non-syndromic intellectual disability 33","mondo","0014580"
< "0070060","autosomal dominant non-syndromic intellectual disability 30","mondo","0014486"
< "0070061","autosomal dominant non-syndromic intellectual disability 31","mondo","0014512"
< "2431","glomus tumor","mesh","D005918"
< "2431","glomus tumor","umls","C0017653"
< "2431","glomus tumor","mondo","0018327"
< "0070068","autosomal dominant non-syndromic intellectual disability 38","mondo","0014617"
< "0070069","autosomal dominant non-syndromic intellectual disability 39","mondo","0014678"
< "8986","narcolepsy","icd10cm","G47.41"
< "8986","narcolepsy","icd10cm","G47.419"
< "8986","narcolepsy","icd9cm","347.0"
< "8986","narcolepsy","mesh","D009290"
< "8986","narcolepsy","umls","C0027404"
< "8986","narcolepsy","mondo","0021107"
---
> "2218","blood platelet disease","mesh","D001791"
> "2218","blood platelet disease","umls","C0005818"
> "2218","blood platelet disease","mondo","0000009"
> "0080348","Alzheimer's disease 1","mondo","0007088"
2896,2911c7877,7878
< "0050428","nonepidermolytic palmoplantar keratoderma","mesh","D015776"
< "0050428","nonepidermolytic palmoplantar keratoderma","umls","C0022584"
< "0050428","nonepidermolytic palmoplantar keratoderma","umls","C3489771"
< "0050428","nonepidermolytic palmoplantar keratoderma","mondo","0006588"
< "0050429","Hailey-Hailey disease","icd10cm","Q82.8"
< "0050429","Hailey-Hailey disease","mesh","D016506"
< "0050429","Hailey-Hailey disease","umls","C0085106"
< "0050429","Hailey-Hailey disease","mondo","0008218"
< "0050424","familial adenomatous polyposis","mesh","D011125"
< "0050424","familial adenomatous polyposis","umls","C0032580"
< "0050424","familial adenomatous polyposis","mondo","0021055"
< "0050425","restless legs syndrome","icd10cm","G25.81"
< "0050425","restless legs syndrome","icd9cm","333.94"
< "0050425","restless legs syndrome","mesh","D012148"
< "0050425","restless legs syndrome","umls","C0035258"
< "0050425","restless legs syndrome","mondo","0005391"
---
> "0080342","Simpson-Golabi-Behmel syndrome type 2","mondo","0010265"
> "0080343","autosomal recessive pyridoxine-refractory sideroblastic anemia 3","mondo","0014804"
2913,2926c7880,7884
< "883","parasitic helminthiasis infectious disease","icd10cm","B65-B83"
< "883","parasitic helminthiasis infectious disease","icd10cm","B83.9"
< "883","parasitic helminthiasis infectious disease","icd9cm","120-129.99"
< "883","parasitic helminthiasis infectious disease","icd9cm","128.9"
< "883","parasitic helminthiasis infectious disease","mesh","D006373"
< "883","parasitic helminthiasis infectious disease","umls","C0018889"
< "883","parasitic helminthiasis infectious disease","mondo","0004664"
< "5936","ovarian mixed germ cell neoplasm","umls","C0280135"
< "5936","ovarian mixed germ cell neoplasm","mondo","0003710"
< "12118","pulmonary hemosiderosis","icd10cm","J84.03"
< "12118","pulmonary hemosiderosis","icd9cm","516.1"
< "12118","pulmonary hemosiderosis","mesh","C536281"
< "12118","pulmonary hemosiderosis","umls","C0020807"
< "12118","pulmonary hemosiderosis","mondo","0008346"
---
> "0080345","blepharocheilodontic syndrome 1","mondo","0054740"
> "0080346","blepharocheilodontic syndrome 2","mondo","0040503"
> "0080347","malignant pheochromocytoma","mondo","0006288"
> "4512","conventional angiosarcoma","umls","C1333155"
> "4512","conventional angiosarcoma","mondo","0003025"
2943,2972c7901,7916
< "0111158","SADDAN","mesh","D000130"
< "0111158","SADDAN","umls","C2674173"
< "0111158","SADDAN","mondo","0014658"
< "2508","Takayasu's arteritis","icd10cm","M31.4"
< "2508","Takayasu's arteritis","icd9cm","446.7"
< "2508","Takayasu's arteritis","mesh","D001015"
< "2508","Takayasu's arteritis","mesh","D013625"
< "2508","Takayasu's arteritis","umls","C0003490"
< "2508","Takayasu's arteritis","umls","C0039263"
< "2508","Takayasu's arteritis","mondo","0017991"
< "0111154","postural orthostatic tachycardia syndrome","icd10cm","I95.1"
< "0111154","postural orthostatic tachycardia syndrome","mesh","D054972"
< "0111154","postural orthostatic tachycardia syndrome","mondo","0011479"
< "0111155","autosomal recessive spinocerebellar ataxia 21","mondo","0014744"
< "0111156","spermatogenic failure 9","mondo","0015746"
< "0111157","Castleman disease","icd10cm","D47.Z2"
< "0111157","Castleman disease","mesh","C536362"
< "0111157","Castleman disease","mesh","D005871"
< "0111157","Castleman disease","umls","C0017531"
< "0111157","Castleman disease","umls","C2931179"
< "0111157","Castleman disease","mondo","0015564"
< "0111150","autosomal dominant isolated ectopia lentis 1","mesh","C536184"
< "0111150","autosomal dominant isolated ectopia lentis 1","umls","C1851286"
< "0111150","autosomal dominant isolated ectopia lentis 1","mondo","0007514"
< "0110304","autosomal dominant limb-girdle muscular dystrophy type 2","icd10cm","G71.0"
< "0110304","autosomal dominant limb-girdle muscular dystrophy type 2","mondo","0012034"
< "0111152","multicentric Castleman disease","mesh","C537372"
< "0111152","multicentric Castleman disease","umls","C1334815"
< "0111152","multicentric Castleman disease","mondo","0019754"
< "0111153","congenital mirror movement disorder","mondo","0016558"
---
> "9423","blepharitis","icd10cm","H01.0"
> "9423","blepharitis","icd10cm","H01.00"
> "9423","blepharitis","icd10cm","H01.9"
> "9423","blepharitis","icd9cm","373.0"
> "9423","blepharitis","icd9cm","373.00"
> "9423","blepharitis","icd9cm","373.4"
> "9423","blepharitis","icd9cm","373.9"
> "9423","blepharitis","mesh","D001762"
> "9423","blepharitis","umls","C0005741"
> "9423","blepharitis","umls","C0155181"
> "9423","blepharitis","mondo","0004785"
> "9427","hypertensive encephalopathy","icd10cm","I67.4"
> "9427","hypertensive encephalopathy","icd9cm","437.2"
> "9427","hypertensive encephalopathy","mesh","D020343"
> "9427","hypertensive encephalopathy","umls","C0151620"
> "9427","hypertensive encephalopathy","mondo","0006796"
2975,2993c7919,7924
< "9352","type 2 diabetes mellitus","kegg","04930"
< "9352","type 2 diabetes mellitus","icd10cm","E11"
< "9352","type 2 diabetes mellitus","mesh","D003924"
< "9352","type 2 diabetes mellitus","umls","C0011860"
< "9352","type 2 diabetes mellitus","mondo","0005148"
< "0050546","congenital adrenal insufficiency","mondo","0013400"
< "2723","dermatitis","icd10cm","L30.9"
< "2723","dermatitis","mesh","D003872"
< "2723","dermatitis","umls","C0011603"
< "2723","dermatitis","mondo","0002406"
< "11037","dissociative amnesia","icd10cm","F44.0"
< "11037","dissociative amnesia","icd9cm","300.12"
< "11037","dissociative amnesia","mesh","D000647"
< "11037","dissociative amnesia","umls","C0236795"
< "11037","dissociative amnesia","mondo","0001185"
< "5207","monodermal teratoma","umls","C1302569"
< "5207","monodermal teratoma","mondo","0003331"
< "0110682","congenital myasthenic syndrome 16","mondo","0013620"
< "0110681","congenital myasthenic syndrome 2A","mondo","0014581"
---
> "5288","larynx leiomyosarcoma","umls","C1334371"
> "5288","larynx leiomyosarcoma","mondo","0003374"
> "5280","gastric leiomyosarcoma","umls","C0744295"
> "5280","gastric leiomyosarcoma","mondo","0003367"
> "5283","vagina leiomyosarcoma","umls","C1336940"
> "5283","vagina leiomyosarcoma","mondo","0003369"
2997a7929
> "5284","retroperitoneal leiomyosarcoma","mondo","0003370"
3000,3043c7932
< "0060785","adult-onset autosomal dominant demyelinating leukodystrophy","umls","C3164344"
< "0060785","adult-onset autosomal dominant demyelinating leukodystrophy","mondo","0008215"
< "7233","adult central nervous system embryonal carcinoma","umls","C1370503"
< "7233","adult central nervous system embryonal carcinoma","mondo","0004155"
< "7231","pediatric CNS embryonal cell carcinoma","umls","C1377605"
< "7231","pediatric CNS embryonal cell carcinoma","mondo","0004153"
< "0050640","anauxetic dysplasia 1","mondo","0011773"
< "14512","candidal paronychia","icd10cm","B37.2"
< "14512","candidal paronychia","icd9cm","112.3"
< "14512","candidal paronychia","umls","C0006842"
< "14512","candidal paronychia","mondo","0001984"
< "0050644","arterial calcification of infancy","mesh","C537440"
< "0050644","arterial calcification of infancy","mondo","0018870"
< "0050646","distal arthrogryposis","mondo","0019942"
< "0050647","Arts syndrome","mesh","C535388"
< "0050647","Arts syndrome","umls","C0796028"
< "0050647","Arts syndrome","mondo","0010533"
< "0110179","Charcot-Marie-Tooth disease type 2B2","icd10cm","G60.0"
< "0110179","Charcot-Marie-Tooth disease type 2B2","mondo","0011570"
< "0110178","Charcot-Marie-Tooth disease axonal type 2V","mondo","0014665"
< "0110175","Charcot-Marie-Tooth disease axonal type 2O","icd10cm","G60.0"
< "0110175","Charcot-Marie-Tooth disease axonal type 2O","mondo","0013644"
< "0110174","Charcot-Marie-Tooth disease axonal type 2L","icd10cm","G60.0"
< "0110174","Charcot-Marie-Tooth disease axonal type 2L","mondo","0012096"
< "0110177","Charcot-Marie-Tooth disease axonal type 2N","icd10cm","G60.0"
< "0110177","Charcot-Marie-Tooth disease axonal type 2N","mondo","0013212"
< "0110176","Charcot-Marie-Tooth disease axonal type 2X","mondo","0014726"
< "0110171","Charcot-Marie-Tooth disease axonal type 2S","mondo","0014511"
< "13444","glanders","icd10cm","A24.0"
< "13444","glanders","icd9cm","024"
< "13444","glanders","mesh","D005896"
< "13444","glanders","umls","C0017589"
< "13444","glanders","mondo","0005774"
< "0110173","Charcot-Marie-Tooth disease axonal type 2U","icd10cm","G60.0"
< "0110173","Charcot-Marie-Tooth disease axonal type 2U","mondo","0014566"
< "10773","bubonic plague","icd10cm","A20.0"
< "10773","bubonic plague","icd9cm","020.0"
< "10773","bubonic plague","mesh","D010930"
< "10773","bubonic plague","umls","C0282312"
< "10773","bubonic plague","mondo","0001112"
< "4994","adenomyoma of uterine corpus","umls","C1336903"
< "4994","adenomyoma of uterine corpus","mondo","0003237"
< "4993","atypical polypoid adenomyoma","umls","C1300347"
< "4993","atypical polypoid adenomyoma","mondo","0003236"
---
> "5286","vulvar leiomyosarcoma","mondo","0003372"
3052,3055c7941,7942
< "12206","dengue hemorrhagic fever","icd10cm","A91"
< "12206","dengue hemorrhagic fever","mesh","D019595"
< "12206","dengue hemorrhagic fever","umls","C0019100"
< "12206","dengue hemorrhagic fever","mondo","0005358"
---
> "0110775","hereditary spastic paraplegia 24","icd10cm","G11.4"
> "0110775","hereditary spastic paraplegia 24","mondo","0011862"
3064,3120c7951,7960
< "0110714","congenital stationary night blindness 1G","mondo","0014614"
< "0110197","Charcot-Marie-Tooth disease dominant intermediate B","icd10cm","G60.0"
< "0110197","Charcot-Marie-Tooth disease dominant intermediate B","mondo","0011674"
< "0110196","Charcot-Marie-Tooth disease type 4G","icd10cm","G60.0"
< "0110196","Charcot-Marie-Tooth disease type 4G","mondo","0011534"
< "0110195","Charcot-Marie-Tooth disease type 4E","icd10cm","G60.0"
< "0110195","Charcot-Marie-Tooth disease type 4E","mondo","0011527"
< "0110194","Charcot-Marie-Tooth disease type 4B3","icd10cm","G60.0"
< "0110194","Charcot-Marie-Tooth disease type 4B3","mondo","0014117"
< "0110193","Charcot-Marie-Tooth disease type 4F","icd10cm","G60.0"
< "0110193","Charcot-Marie-Tooth disease type 4F","mondo","0013959"
< "0110192","Charcot-Marie-Tooth disease type 4H","icd10cm","G60.0"
< "0110192","Charcot-Marie-Tooth disease type 4H","mondo","0012250"
< "0110191","Charcot-Marie-Tooth disease type 4B1","icd10cm","G60.0"
< "0110191","Charcot-Marie-Tooth disease type 4B1","mondo","0011066"
< "0110190","Charcot-Marie-Tooth disease type 4B2","icd10cm","G60.0"
< "0110190","Charcot-Marie-Tooth disease type 4B2","mondo","0011475"
< "11824","multicentric reticulohistiocytosis","icd10cm","E78.81"
< "11824","multicentric reticulohistiocytosis","umls","C0311284"
< "11824","multicentric reticulohistiocytosis","mondo","0015347"
< "0002116","pterygium","mesh","D011625"
< "0002116","pterygium","umls","C0033999"
< "0002116","pterygium","mondo","0005085"
< "0110199","Charcot-Marie-Tooth disease dominant intermediate C","icd10cm","G60.0"
< "0110199","Charcot-Marie-Tooth disease dominant intermediate C","mondo","0012012"
< "14670","hypertelorism, microtia, facial clefting syndrome","mesh","C537632"
< "14670","hypertelorism, microtia, facial clefting syndrome","umls","C0220742"
< "14670","hypertelorism, microtia, facial clefting syndrome","mondo","0009404"
< "10518","beach ear","icd9cm","380.12"
< "10518","beach ear","umls","C0155393"
< "10518","beach ear","mondo","0001051"
< "10519","chronic fungal otitis externa","icd9cm","380.15"
< "10519","chronic fungal otitis externa","umls","C0155396"
< "10519","chronic fungal otitis externa","mondo","0001052"
< "11038","depersonalization disorder","icd9cm","300.6"
< "11038","depersonalization disorder","mesh","D003861"
< "11038","depersonalization disorder","umls","C0683416"
< "11038","depersonalization disorder","mondo","0001186"
< "90","degenerative disc disease","umls","C0410606"
< "90","degenerative disc disease","mondo","0011385"
< "3711","bladder adenocarcinoma","umls","C0279682"
< "3711","bladder adenocarcinoma","mondo","0002751"
< "5265","lung leiomyosarcoma","umls","C1334448"
< "5265","lung leiomyosarcoma","mondo","0003357"
< "0050568","spondylocostal dysostosis","mondo","0000359"
< "8864","acute monocytic leukemia","icd9cm","206.0"
< "8864","acute monocytic leukemia","mesh","D007948"
< "8864","acute monocytic leukemia","umls","C0023465"
< "8864","acute monocytic leukemia","mondo","0007896"
< "1949","cholecystitis","icd10cm","K81"
< "1949","cholecystitis","icd10cm","K81.9"
< "1949","cholecystitis","icd9cm","575.10"
< "1949","cholecystitis","mesh","D002764"
< "1949","cholecystitis","umls","C0008325"
< "1949","cholecystitis","mondo","0002155"
< "3498","pancreatic ductal adenocarcinoma","umls","C1335302"
< "3498","pancreatic ductal adenocarcinoma","mondo","0005184"
---
> "0110770","hereditary spastic paraplegia 17","icd10cm","G11.4"
> "0110770","hereditary spastic paraplegia 17","mondo","0010043"
> "14264","benign neonatal seizures","mesh","D020936"
> "14264","benign neonatal seizures","umls","C0270851"
> "14264","benign neonatal seizures","mondo","0016027"
> "7302","endodermal sinus pattern testicular yolk sac tumor","umls","C1515303"
> "7302","endodermal sinus pattern testicular yolk sac tumor","mondo","0004178"
> "14265","pulmonary valve insufficiency","mesh","D011665"
> "14265","pulmonary valve insufficiency","umls","C0034088"
> "14265","pulmonary valve insufficiency","mondo","0001927"
3122c7962,7964
< "0070249","autosomal dominant Emery-Dreifuss muscular dystrophy 4","mondo","0013071"
---
> "7305","astroblastoma","mesh","D018302"
> "7305","astroblastoma","umls","C0334587"
> "7305","astroblastoma","mondo","0016707"
3126,3136c7968,7969
< "13087","Lown-Ganong-Levine syndrome","icd10cm","I45.6"
< "13087","Lown-Ganong-Levine syndrome","icd9cm","426.81"
< "13087","Lown-Ganong-Levine syndrome","mesh","D008151"
< "13087","Lown-Ganong-Levine syndrome","umls","C0024054"
< "13087","Lown-Ganong-Levine syndrome","mondo","0007174"
< "9286","priapism","icd10cm","N48.3"
< "9286","priapism","icd10cm","N48.30"
< "9286","priapism","icd9cm","607.3"
< "9286","priapism","mesh","D011317"
< "9286","priapism","umls","C0033117"
< "9286","priapism","mondo","0004745"
---
> "0070244","primary coenzyme Q10 deficiency 7","mondo","0014562"
> "0070245","primary coenzyme Q10 deficiency 8","mondo","0014754"
3138,3140c7971,7982
< "0070243","primary coenzyme Q10 deficiency 6","mondo","0013836"
< "0070240","primary coenzyme Q10 deficiency 3","mondo","0013838"
< "0070241","primary coenzyme Q10 deficiency 4","mondo","0012784"
---
> "9280","carbamoyl phosphate synthetase I deficiency disease","mesh","D020165"
> "9280","carbamoyl phosphate synthetase I deficiency disease","umls","C0751753"
> "9280","carbamoyl phosphate synthetase I deficiency disease","mondo","0009376"
> "9283","borderline glaucoma","icd10cm","H40.00"
> "9283","borderline glaucoma","icd9cm","365.00"
> "9283","borderline glaucoma","umls","C0549470"
> "9283","borderline glaucoma","mondo","0004744"
> "9282","ocular hypertension","icd10cm","H40.05"
> "9282","ocular hypertension","icd9cm","365.04"
> "9282","ocular hypertension","mesh","D009798"
> "9282","ocular hypertension","umls","C0028840"
> "9282","ocular hypertension","mondo","0006875"
3144a7987,7991
> "11914","gastroparesis","icd10cm","K31.84"
> "11914","gastroparesis","icd9cm","536.3"
> "11914","gastroparesis","mesh","D018589"
> "11914","gastroparesis","umls","C0152020"
> "11914","gastroparesis","mondo","0006769"
3164,3167c8011,8014
< "0110221","Brugada syndrome 4","icd10cm","I49.8"
< "0110221","Brugada syndrome 4","mondo","0012743"
< "0110220","Brugada syndrome 3","icd10cm","I49.8"
< "0110220","Brugada syndrome 3","mondo","0012742"
---
> "12932","endomyocardial fibrosis","icd9cm","425.0"
> "12932","endomyocardial fibrosis","mesh","D004719"
> "12932","endomyocardial fibrosis","umls","C0553980"
> "12932","endomyocardial fibrosis","mondo","0006746"
3173,3226c8020,8048
< "0110222","Brugada syndrome 5","icd10cm","I49.8"
< "0110222","Brugada syndrome 5","mondo","0013015"
< "0110225","Brugada syndrome 8","icd10cm","I49.8"
< "0110225","Brugada syndrome 8","mondo","0013148"
< "0110224","Brugada syndrome 7","icd10cm","I49.8"
< "0110224","Brugada syndrome 7","mondo","0013146"
< "0110227","cataract 32 multiple types","icd10cm","Q12.0"
< "0110227","cataract 32 multiple types","mondo","0007278"
< "0110611","primary ciliary dyskinesia 27","icd10cm","Q34.8"
< "0110611","primary ciliary dyskinesia 27","mondo","0014215"
< "0110229","cataract 6 multiple types","icd10cm","Q12.0"
< "0110229","cataract 6 multiple types","mondo","0007288"
< "0110228","cataract 8 multiple types","icd10cm","Q12.0"
< "0110228","cataract 8 multiple types","mondo","0007280"
< "0070244","primary coenzyme Q10 deficiency 7","mondo","0014562"
< "0070275","hereditary nonpolyposis colorectal cancer type 4","mondo","0013699"
< "9477","pulmonary embolism","icd10cm","I26"
< "9477","pulmonary embolism","icd10cm","I26.99"
< "9477","pulmonary embolism","mesh","D011655"
< "9477","pulmonary embolism","umls","C0034065"
< "9477","pulmonary embolism","mondo","0005279"
< "10206","lipoma of spermatic cord","icd9cm","214.4"
< "10206","lipoma of spermatic cord","umls","C0153972"
< "10206","lipoma of spermatic cord","mondo","0000975"
< "14218","dihydropyrimidine dehydrogenase deficiency","mesh","D054067"
< "14218","dihydropyrimidine dehydrogenase deficiency","umls","C1959620"
< "14218","dihydropyrimidine dehydrogenase deficiency","umls","C3495551"
< "14218","dihydropyrimidine dehydrogenase deficiency","mondo","0010130"
< "10205","axillary lipoma","umls","C0347429"
< "10205","axillary lipoma","mondo","0000974"
< "5465","conjunctival intraepithelial neoplasm","umls","C1333148"
< "5465","conjunctival intraepithelial neoplasm","mondo","0003453"
< "1495","cystic echinococcosis","icd10cm","B67.4"
< "1495","cystic echinococcosis","icd9cm","122.4"
< "1495","cystic echinococcosis","umls","C0152068"
< "1495","cystic echinococcosis","mondo","0018408"
< "1496","echinococcosis","icd10cm","B67"
< "1496","echinococcosis","icd10cm","B67.90"
< "1496","echinococcosis","icd9cm","122"
< "1496","echinococcosis","mesh","D004443"
< "1496","echinococcosis","umls","C0013502"
< "1496","echinococcosis","mondo","0005738"
< "10201","gallbladder lipoma","umls","C1333747"
< "10201","gallbladder lipoma","mondo","0000972"
< "1498","cholera","icd10cm","A00"
< "1498","cholera","icd10cm","A00.0"
< "1498","cholera","icd10cm","A00.9"
< "1498","cholera","icd9cm","001"
< "1498","cholera","icd9cm","001.0"
< "1498","cholera","icd9cm","001.9"
< "1498","cholera","mesh","D002771"
< "1498","cholera","umls","C0008354"
< "1498","cholera","mondo","0015766"
< "0070273","hereditary nonpolyposis colorectal cancer type 6","mondo","0013695"
---
> "12934","Kearns-Sayre syndrome","icd10cm","H49.81"
> "12934","Kearns-Sayre syndrome","mesh","D007625"
> "12934","Kearns-Sayre syndrome","umls","C0022541"
> "12934","Kearns-Sayre syndrome","mondo","0010787"
> "12935","alcoholic cardiomyopathy","icd10cm","I42.6"
> "12935","alcoholic cardiomyopathy","icd9cm","425.5"
> "12935","alcoholic cardiomyopathy","mesh","D002310"
> "12935","alcoholic cardiomyopathy","umls","C0007192"
> "12935","alcoholic cardiomyopathy","mondo","0006643"
> "0111276","sensory ataxic neuropathy, dysarthria, and ophthalmoparesis","mesh","C537583"
> "0111276","sensory ataxic neuropathy, dysarthria, and ophthalmoparesis","umls","C1843851"
> "7045","basaloid lung carcinoma","umls","C1332463"
> "7045","basaloid lung carcinoma","mondo","0004087"
> "10207","paratesticular lipoma","umls","C1335348"
> "10207","paratesticular lipoma","mondo","0000976"
> "7047","penis basaloid carcinoma","umls","C1332462"
> "7047","penis basaloid carcinoma","mondo","0004089"
> "7046","cervical basaloid squamous cell carcinoma","umls","C1511063"
> "7046","cervical basaloid squamous cell carcinoma","mondo","0004088"
> "7041","choroid epithelioid cell melanoma","umls","C1333024"
> "7041","choroid epithelioid cell melanoma","mondo","0004085"
> "7040","uveal epithelioid cell melanoma","umls","C1333422"
> "7040","uveal epithelioid cell melanoma","mondo","0006200"
> "10200","chest wall lipoma","umls","C1332932"
> "10200","chest wall lipoma","mondo","0000971"
> "7042","ciliary body epithelioid cell melanoma","umls","C1333050"
> "7042","ciliary body epithelioid cell melanoma","mondo","0004086"
> "7049","basaloid squamous cell skin carcinoma","umls","C1335973"
> "7049","basaloid squamous cell skin carcinoma","mondo","0004091"
3228,3249c8050,8061
< "1626","breast duct papilloma","umls","C0238034"
< "1626","breast duct papilloma","mondo","0021097"
< "1700","X-linked ichthyosis","icd10cm","Q80.1"
< "1700","X-linked ichthyosis","mesh","D016114"
< "1700","X-linked ichthyosis","umls","C0079588"
< "1700","X-linked ichthyosis","mondo","0010622"
< "14188","frozen shoulder","icd10cm","M75.0"
< "14188","frozen shoulder","icd9cm","726.0"
< "14188","frozen shoulder","mesh","D002062"
< "14188","frozen shoulder","umls","C0311223"
< "14188","frozen shoulder","mondo","0006763"
< "1702","ichthyosis vulgaris","icd10cm","Q80.0"
< "1702","ichthyosis vulgaris","mesh","D016112"
< "1702","ichthyosis vulgaris","umls","C0079584"
< "1702","ichthyosis vulgaris","mondo","0007810"
< "1394","urinary schistosomiasis","icd9cm","120.0"
< "1394","urinary schistosomiasis","mesh","D012553"
< "1394","urinary schistosomiasis","umls","C0276926"
< "1394","urinary schistosomiasis","mondo","0006001"
< "10192","pleomorphic lipoma","mesh","D008067"
< "10192","pleomorphic lipoma","umls","C0205823"
< "10192","pleomorphic lipoma","mondo","0000966"
---
> "10208","chondroid lipoma","umls","C1266131"
> "10208","chondroid lipoma","mondo","0000977"
> "10209","extrahepatic bile duct lipoma","umls","C1333509"
> "10209","extrahepatic bile duct lipoma","mondo","0000978"
> "13368","tinea profunda","umls","C1279621"
> "13368","tinea profunda","mondo","0001698"
> "0060319","cardiac arrest","icd10cm","I46"
> "0060319","cardiac arrest","icd9cm","427.5"
> "0060319","cardiac arrest","mesh","D006323"
> "0060319","cardiac arrest","umls","C0018790"
> "0060319","cardiac arrest","umls","C0600228"
> "0060319","cardiac arrest","mondo","0000745"
3255,3256d8066
< "5260","colon sarcoma","umls","C1333098"
< "5260","colon sarcoma","mondo","0003352"
3261,3262c8071,8081
< "1996","rectum adenocarcinoma","umls","C0149978"
< "1996","rectum adenocarcinoma","mondo","0002169"
---
> "0060317","lung abscess","icd10cm","J85.2"
> "0060317","lung abscess","icd9cm","513.0"
> "0060317","lung abscess","mesh","D008169"
> "0060317","lung abscess","umls","C0024110"
> "0060317","lung abscess","mondo","0000744"
> "0060316","orofaciodigital syndrome I","icd10cm","Q87.0"
> "0060316","orofaciodigital syndrome I","mesh","D009958"
> "0060316","orofaciodigital syndrome I","umls","C0026363"
> "0060316","orofaciodigital syndrome I","umls","C0029294"
> "0060316","orofaciodigital syndrome I","umls","C1510460"
> "0060316","orofaciodigital syndrome I","mondo","0010702"
3274,3305c8093,8107
< "10199","breast lipoma","umls","C0349565"
< "10199","breast lipoma","mondo","0000970"
< "0110427","dilated cardiomyopathy 1V","icd10cm","I42.0"
< "0110427","dilated cardiomyopathy 1V","mondo","0013373"
< "0110426","dilated cardiomyopathy 1D","icd10cm","I42.0"
< "0110426","dilated cardiomyopathy 1D","mondo","0011095"
< "0110425","dilated cardiomyopathy 1A","mondo","0007269"
< "0110424","dilated cardiomyopathy 1CC","icd10cm","I42.0"
< "0110424","dilated cardiomyopathy 1CC","mondo","0013147"
< "0110423","dilated cardiomyopathy 1C","icd10cm","I42.0"
< "0110423","dilated cardiomyopathy 1C","mondo","0011094"
< "0110350","osteogenesis imperfecta type 6","icd10cm","Q78.0"
< "0110350","osteogenesis imperfecta type 6","mondo","0013515"
< "0110353","retinitis pigmentosa 20","icd10cm","H35.5"
< "0110353","retinitis pigmentosa 20","mondo","0013425"
< "0110352","retinitis pigmentosa 59","icd10cm","H35.5"
< "0110352","retinitis pigmentosa 59","mondo","0013468"
< "0110359","retinitis pigmentosa 67","icd10cm","H35.5"
< "0110359","retinitis pigmentosa 67","mondo","0014256"
< "0110358","retinitis pigmentosa 12","icd10cm","H35.5"
< "0110358","retinitis pigmentosa 12","mondo","0010818"
< "0110429","dilated cardiomyopathy 1H","icd10cm","I42.0"
< "0110429","dilated cardiomyopathy 1H","mondo","0011425"
< "0110428","dilated cardiomyopathy 1AA","icd10cm","I42.0"
< "0110428","dilated cardiomyopathy 1AA","mondo","0012808"
< "0050769","N syndrome","mondo","0010686"
< "4079","heart valve disease","mesh","D006349"
< "4079","heart valve disease","mesh","D016127"
< "4079","heart valve disease","umls","C0018824"
< "4079","heart valve disease","umls","C0079485"
< "4079","heart valve disease","mondo","0002869"
< "0111104","maturity-onset diabetes of the young type 6","mondo","0011668"
---
> "0060312","angular cheilitis","icd10cm","K13.0"
> "0060312","angular cheilitis","umls","C0221237"
> "0060312","angular cheilitis","mondo","0000741"
> "6988","peripheral epithelioid sarcoma","umls","C1333306"
> "6988","peripheral epithelioid sarcoma","mondo","0004060"
> "8602","gum cancer","icd10cm","C03"
> "8602","gum cancer","icd10cm","C03.9"
> "8602","gum cancer","icd9cm","143"
> "8602","gum cancer","icd9cm","143.9"
> "8602","gum cancer","umls","C0153364"
> "8602","gum cancer","mondo","0005507"
> "8601","upper gum cancer","icd10cm","C03.0"
> "8601","upper gum cancer","icd9cm","143.0"
> "8601","upper gum cancer","umls","C0153365"
> "8601","upper gum cancer","mondo","0004615"
3309,3333d8110
< "14325","mixed malaria","icd9cm","084.5"
< "14325","mixed malaria","umls","C0153121"
< "14325","mixed malaria","mondo","0001944"
< "14324","Plasmodium malariae malaria","icd10cm","B52"
< "14324","Plasmodium malariae malaria","icd10cm","B52.9"
< "14324","Plasmodium malariae malaria","icd9cm","084.2"
< "14324","Plasmodium malariae malaria","umls","C0024536"
< "14324","Plasmodium malariae malaria","mondo","0001943"
< "14453","farmer's lung","icd10cm","J67.0"
< "14453","farmer's lung","icd9cm","495.0"
< "14453","farmer's lung","mesh","D005203"
< "14453","farmer's lung","umls","C0015634"
< "14453","farmer's lung","mondo","0001971"
< "3209","junctional epidermolysis bullosa","mesh","D016109"
< "3209","junctional epidermolysis bullosa","umls","C0079301"
< "3209","junctional epidermolysis bullosa","mondo","0017612"
< "14323","Marfan syndrome","icd10cm","Q87.4"
< "14323","Marfan syndrome","icd10cm","Q87.40"
< "14323","Marfan syndrome","icd9cm","759.82"
< "14323","Marfan syndrome","mesh","D008382"
< "14323","Marfan syndrome","umls","C0024796"
< "14323","Marfan syndrome","mondo","0007947"
< "14450","46 XX gonadal dysgenesis","mesh","D023961"
< "14450","46 XX gonadal dysgenesis","umls","C0949595"
< "14450","46 XX gonadal dysgenesis","mondo","0009299"
3338,3339c8115,8116
< "0110544","autosomal dominant nonsyndromic deafness 12","icd10cm","H90.3"
< "0110544","autosomal dominant nonsyndromic deafness 12","mondo","0011102"
---
> "0050894","ameloblastoma","mesh","D000564"
> "0050894","ameloblastoma","mondo","0017795"
3344,3350c8121,8136
< "4765","pulmonary blastoma","mesh","D018202"
< "4765","pulmonary blastoma","umls","C0206629"
< "4765","pulmonary blastoma","mondo","0005933"
< "0110013","advanced sleep phase syndrome 3","mondo","0014814"
< "3025","acinar cell carcinoma","mesh","D018267"
< "3025","acinar cell carcinoma","umls","C0206685"
< "3025","acinar cell carcinoma","mondo","0004965"
---
> "14693","Clouston syndrome","mesh","D004476"
> "14693","Clouston syndrome","umls","C0162361"
> "14693","Clouston syndrome","mondo","0007510"
> "14692","Smith-Lemli-Opitz syndrome","icd10cm","E78.72"
> "14692","Smith-Lemli-Opitz syndrome","mesh","D019082"
> "14692","Smith-Lemli-Opitz syndrome","umls","C0175694"
> "14692","Smith-Lemli-Opitz syndrome","mondo","0010035"
> "2983","anuria","mesh","D001002"
> "2983","anuria","umls","C0003460"
> "2983","anuria","mondo","0002476"
> "2982","perinephritis","mesh","D010501"
> "2982","perinephritis","umls","C0031065"
> "2982","perinephritis","mondo","0006900"
> "2981","kidney papillary necrosis","mesh","D007681"
> "2981","kidney papillary necrosis","umls","C0022667"
> "2981","kidney papillary necrosis","mondo","0006821"
3356,3437c8142,8164
< "0110546","autosomal dominant nonsyndromic deafness 15","icd10cm","H90.3"
< "0110546","autosomal dominant nonsyndromic deafness 15","mondo","0011226"
< "3651","pyruvate carboxylase deficiency disease","icd10cm","E74.4"
< "3651","pyruvate carboxylase deficiency disease","mesh","D015324"
< "3651","pyruvate carboxylase deficiency disease","umls","C0034341"
< "3651","pyruvate carboxylase deficiency disease","mondo","0009949"
< "526","human immunodeficiency virus infectious disease","icd10cm","B20"
< "526","human immunodeficiency virus infectious disease","icd10cm","B20-B20"
< "526","human immunodeficiency virus infectious disease","icd9cm","042"
< "526","human immunodeficiency virus infectious disease","icd9cm","042-042.99"
< "526","human immunodeficiency virus infectious disease","mesh","D015658"
< "526","human immunodeficiency virus infectious disease","umls","C0019693"
< "526","human immunodeficiency virus infectious disease","mondo","0005109"
< "0110547","autosomal dominant nonsyndromic deafness 16","icd10cm","H90.3"
< "0110547","autosomal dominant nonsyndromic deafness 16","mondo","0011389"
< "520","aortic disease","mesh","D001018"
< "520","aortic disease","umls","C0003493"
< "520","aortic disease","mondo","0005561"
< "13366","Stiff-Person syndrome","icd10cm","G25.82"
< "13366","Stiff-Person syndrome","icd9cm","333.91"
< "13366","Stiff-Person syndrome","mesh","D016750"
< "13366","Stiff-Person syndrome","umls","C0085292"
< "13366","Stiff-Person syndrome","mondo","0008491"
< "8736","smallpox","icd10cm","B03"
< "8736","smallpox","icd9cm","050"
< "8736","smallpox","icd9cm","050.9"
< "8736","smallpox","mesh","D012899"
< "8736","smallpox","umls","C0037354"
< "8736","smallpox","mondo","0004651"
< "0110016","Leber congenital amaurosis 2","icd10cm","H35.5"
< "0110016","Leber congenital amaurosis 2","mondo","0008765"
< "0060898","early-onset Parkinson's disease 20","mondo","0014233"
< "0060264","pontocerebellar hypoplasia","mesh","C580383"
< "0060264","pontocerebellar hypoplasia","umls","C0266468"
< "0060264","pontocerebellar hypoplasia","mondo","0020135"
< "0110017","age related macular degeneration 4","mondo","0012540"
< "12594","Potter's syndrome","icd10cm","Q60.6"
< "12594","Potter's syndrome","umls","C0178426"
< "12594","Potter's syndrome","mondo","0001558"
< "2832","geotrichosis","icd10cm","B48.3"
< "2832","geotrichosis","mesh","D005847"
< "2832","geotrichosis","umls","C0017455"
< "2832","geotrichosis","mondo","0005772"
< "8515","Cor pulmonale","icd10cm","I27.81"
< "8515","Cor pulmonale","icd10cm","I27.9"
< "8515","Cor pulmonale","mesh","D011660"
< "8515","Cor pulmonale","umls","C0034072"
< "8515","Cor pulmonale","mondo","0004596"
< "0110014","age related macular degeneration 1","mondo","0011285"
< "4196","femoral neuropathy","icd10cm","G57.2"
< "4196","femoral neuropathy","icd10cm","G57.20"
< "4196","femoral neuropathy","mesh","D020428"
< "4196","femoral neuropathy","umls","C0751931"
< "4196","femoral neuropathy","mondo","0006759"
< "0110543","autosomal dominant nonsyndromic deafness 11","icd10cm","H90.3"
< "0110543","autosomal dominant nonsyndromic deafness 11","mondo","0011032"
< "14087","epicondylitis","icd10cm","M77.1"
< "14087","epicondylitis","icd9cm","726.32"
< "14087","epicondylitis","mesh","D013716"
< "14087","epicondylitis","umls","C0014488"
< "14087","epicondylitis","umls","C0039516"
< "14087","epicondylitis","mondo","0001875"
< "5670","comedo carcinoma","umls","C0334370"
< "5670","comedo carcinoma","mondo","0003575"
< "0110463","autosomal recessive nonsyndromic deafness 102","icd10cm","H90.3"
< "0110463","autosomal recessive nonsyndromic deafness 102","mondo","0014428"
< "12849","autistic disorder","icd10cm","F84.0"
< "12849","autistic disorder","icd9cm","299.0"
< "12849","autistic disorder","mesh","D001321"
< "12849","autistic disorder","umls","C0004352"
< "12849","autistic disorder","mondo","0005260"
< "5675","cribriform carcinoma","mesh","D000230"
< "5675","cribriform carcinoma","umls","C0205643"
< "5675","cribriform carcinoma","mondo","0045059"
< "0110462","autosomal recessive nonsyndromic deafness 101","icd10cm","H90.3"
< "0110462","autosomal recessive nonsyndromic deafness 101","mondo","0014363"
< "12842","Guillain-Barre syndrome","icd10cm","G61.0"
< "12842","Guillain-Barre syndrome","mesh","D020275"
< "12842","Guillain-Barre syndrome","umls","C0018378"
< "12842","Guillain-Barre syndrome","mondo","0016218"
< "0110393","retinitis pigmentosa 66","icd10cm","H35.5"
< "0110393","retinitis pigmentosa 66","mondo","0014093"
---
> "2986","IgA glomerulonephritis","mesh","D005922"
> "2986","IgA glomerulonephritis","umls","C0017661"
> "2986","IgA glomerulonephritis","mondo","0005342"
> "1019","osteomyelitis","icd9cm","730.1"
> "1019","osteomyelitis","icd9cm","730.10"
> "1019","osteomyelitis","mesh","D010019"
> "1019","osteomyelitis","umls","C0008707"
> "1019","osteomyelitis","mondo","0005246"
> "14262","oral candidiasis","icd10cm","B37.0"
> "14262","oral candidiasis","icd10cm","B37.9"
> "14262","oral candidiasis","icd9cm","112.0"
> "14262","oral candidiasis","mesh","D002180"
> "14262","oral candidiasis","umls","C0006849"
> "14262","oral candidiasis","mondo","0005886"
> "4359","amelanotic melanoma","mesh","D018328"
> "4359","amelanotic melanoma","umls","C0206735"
> "4359","amelanotic melanoma","mondo","0002971"
> "4352","ciliary body cancer","icd10cm","C69.4"
> "4352","ciliary body cancer","umls","C0339349"
> "4352","ciliary body cancer","umls","C0496833"
> "4352","ciliary body cancer","mondo","0002969"
> "4353","ciliary body disease","umls","C0271100"
> "4353","ciliary body disease","mondo","0002970"
3442,3446c8169,8173
< "0110460","dilated cardiomyopathy 2A","icd10cm","I42.0"
< "0110460","dilated cardiomyopathy 2A","mondo","0012746"
< "0060040","pervasive developmental disorder","icd9cm","299.80"
< "0060040","pervasive developmental disorder","umls","C0154451"
< "0060040","pervasive developmental disorder","mondo","0000594"
---
> "14522","partial arterial retinal occlusion","icd10cm","H34.21"
> "14522","partial arterial retinal occlusion","icd10cm","H34.219"
> "14522","partial arterial retinal occlusion","icd9cm","362.33"
> "14522","partial arterial retinal occlusion","umls","C0154839"
> "14522","partial arterial retinal occlusion","mondo","0001985"
3452,3488c8179,8226
< "0110395","retinitis pigmentosa 72","icd10cm","H35.5"
< "0110395","retinitis pigmentosa 72","mondo","0014653"
< "6501","brain stem angioblastoma","umls","C1332611"
< "6501","brain stem angioblastoma","mondo","0003902"
< "8454","ariboflavinosis","icd10cm","E53.0"
< "8454","ariboflavinosis","icd9cm","266.0"
< "8454","ariboflavinosis","mesh","D012257"
< "8454","ariboflavinosis","umls","C0035528"
< "8454","ariboflavinosis","mondo","0004573"
< "0110465","autosomal recessive nonsyndromic deafness 104","icd10cm","H90.3"
< "0110465","autosomal recessive nonsyndromic deafness 104","mondo","0014675"
< "0110464","autosomal recessive nonsyndromic deafness 103","icd10cm","H90.3"
< "0110464","autosomal recessive nonsyndromic deafness 103","mondo","0014469"
< "13564","aspergillosis","icd10cm","B44"
< "13564","aspergillosis","icd10cm","B44.9"
< "13564","aspergillosis","icd9cm","117.3"
< "13564","aspergillosis","mesh","D001228"
< "13564","aspergillosis","umls","C0004030"
< "13564","aspergillosis","mondo","0005657"
< "0090140","cortisone reductase deficiency 2","mondo","0013842"
< "3803","Crigler-Najjar syndrome","icd10cm","E80.5"
< "3803","Crigler-Najjar syndrome","mesh","D003414"
< "3803","Crigler-Najjar syndrome","umls","C0010324"
< "3803","Crigler-Najjar syndrome","mondo","0009044"
< "743","dermatographia","icd10cm","L50.3"
< "743","dermatographia","icd9cm","708.3"
< "743","dermatographia","umls","C0343065"
< "743","dermatographia","mondo","0007448"
< "8466","retinal degeneration","mesh","D012162"
< "8466","retinal degeneration","umls","C0035304"
< "8466","retinal degeneration","mondo","0004580"
< "4907","small intestine carcinoma","umls","C0238196"
< "4907","small intestine carcinoma","mondo","0005522"
< "4906","small intestine adenocarcinoma","umls","C0278803"
< "4906","small intestine adenocarcinoma","mondo","0003198"
< "0090009","immunodeficiency-centromeric instability-facial anomalies syndrome 2","icd10cm","D84.8"
< "0090009","immunodeficiency-centromeric instability-facial anomalies syndrome 2","mondo","0013553"
---
> "14524","senile degeneration of brain","icd9cm","331.2"
> "14524","senile degeneration of brain","umls","C0154669"
> "14524","senile degeneration of brain","mondo","0001987"
> "14529","external pathological resorption","icd10cm","K03.3"
> "14529","external pathological resorption","icd9cm","521.42"
> "14529","external pathological resorption","umls","C0266878"
> "14529","external pathological resorption","mondo","0001988"
> "438","autoimmune disease of the nervous system","mesh","D020274"
> "438","autoimmune disease of the nervous system","umls","C0751871"
> "438","autoimmune disease of the nervous system","mondo","0002977"
> "439","neuromuscular junction disease","mesh","D020511"
> "439","neuromuscular junction disease","umls","C0751950"
> "439","neuromuscular junction disease","mondo","0020124"
> "436","posterior mediastinum cancer","icd10cm","C38.2"
> "436","posterior mediastinum cancer","icd9cm","164.3"
> "436","posterior mediastinum cancer","umls","C0153502"
> "436","posterior mediastinum cancer","mondo","0002972"
> "437","myasthenia gravis","icd10cm","G70.0"
> "437","myasthenia gravis","icd10cm","G70.00"
> "437","myasthenia gravis","icd9cm","358.0"
> "437","myasthenia gravis","icd9cm","358.00"
> "437","myasthenia gravis","mesh","D009157"
> "437","myasthenia gravis","umls","C0026896"
> "437","myasthenia gravis","umls","C1260409"
> "437","myasthenia gravis","mondo","0009688"
> "431","myofascial pain syndrome","mesh","D009209"
> "431","myofascial pain syndrome","umls","C0027073"
> "431","myofascial pain syndrome","mondo","0006862"
> "14305","tuberculous empyema","mesh","D004654"
> "14305","tuberculous empyema","umls","C0014014"
> "14305","tuberculous empyema","mondo","0005999"
> "11342","arcus senilis","icd10cm","H18.41"
> "11342","arcus senilis","mesh","D001112"
> "11342","arcus senilis","umls","C0003742"
> "11342","arcus senilis","mondo","0007150"
> "11343","scleral disease","icd10cm","H15"
> "11343","scleral disease","icd10cm","H15.9"
> "11343","scleral disease","mesh","D015422"
> "11343","scleral disease","umls","C0036412"
> "11343","scleral disease","mondo","0001269"
> "5709","mixed-type liposarcoma","umls","C0545074"
> "5709","mixed-type liposarcoma","mondo","0013280"
> "5704","sclerosing liposarcoma","umls","C0334469"
> "5704","sclerosing liposarcoma","mondo","0003595"
> "5705","spindle cell liposarcoma","umls","C1275275"
> "5705","spindle cell liposarcoma","mondo","0003596"
> "5700","gastric liposarcoma","umls","C1333778"
> "5700","gastric liposarcoma","mondo","0003592"
3491,3536c8229,8240
< "3503","breast signet ring cell adenocarcinoma","umls","C1335964"
< "3503","breast signet ring cell adenocarcinoma","mondo","0002671"
< "699","mitochondrial myopathy","mesh","D017240"
< "699","mitochondrial myopathy","umls","C0162670"
< "699","mitochondrial myopathy","mondo","0009637"
< "0060689","atrichia with papular lesions","icd10cm","L65.8"
< "0060689","atrichia with papular lesions","mondo","0008847"
< "0060688","arteriovenous malformations of the brain","icd10cm","Q28.2"
< "0060688","arteriovenous malformations of the brain","mesh","D002538"
< "0060688","arteriovenous malformations of the brain","umls","C0007772"
< "0060688","arteriovenous malformations of the brain","mondo","0007154"
< "0060686","autosomal dominant nocturnal frontal lobe epilepsy 5","mondo","0014002"
< "0060685","autosomal dominant nocturnal frontal lobe epilepsy 4","mondo","0012474"
< "0060684","autosomal dominant nocturnal frontal lobe epilepsy 3","mondo","0011545"
< "0060683","autosomal dominant nocturnal frontal lobe epilepsy 2","mondo","0011297"
< "0060682","autosomal dominant nocturnal frontal lobe epilepsy 1","mondo","0010899"
< "0060681","autosomal dominant nocturnal frontal lobe epilepsy","mondo","0020300"
< "0060680","pigment dispersion syndrome","mesh","C563184"
< "0060680","pigment dispersion syndrome","mondo","0010896"
< "0080209","sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay","mondo","0014487"
< "0080208","nonalcoholic fatty liver disease","mondo","0013209"
< "0080205","CAKUT","mondo","0019719"
< "0080207","CAKUT2","mondo","0027676"
< "0080206","CAKUT1","mondo","0012561"
< "0080201","Peters plus syndrome","mondo","0009856"
< "4772","mesoblastic nephroma","mesh","D018201"
< "4772","mesoblastic nephroma","umls","C0206628"
< "4772","mesoblastic nephroma","mondo","0003130"
< "4927","Klatskin's tumor","mesh","D018285"
< "4927","Klatskin's tumor","umls","C0206702"
< "4927","Klatskin's tumor","mondo","0003345"
< "0110999","Joubert syndrome 4","mesh","C536296"
< "0110999","Joubert syndrome 4","mondo","0012308"
< "0110998","Joubert syndrome 3","mesh","C536295"
< "0110998","Joubert syndrome 3","mondo","0012078"
< "0110997","Joubert syndrome 28","mondo","0014928"
< "0110996","Joubert syndrome 27","mondo","0014927"
< "0110995","Joubert syndrome 26","mondo","0014771"
< "0110994","Joubert syndrome 25","mondo","0014770"
< "0110993","Joubert syndrome 24","mondo","0014724"
< "0110992","Joubert syndrome 23","mondo","0014664"
< "0110991","Joubert syndrome 22","mondo","0014297"
< "0110990","Joubert syndrome 21","mondo","0014288"
< "6758","chest wall lymphoma","umls","C0346948"
< "6758","chest wall lymphoma","umls","C1332933"
< "6758","chest wall lymphoma","mondo","0003985"
---
> "5702","pleomorphic liposarcoma","mesh","D008080"
> "5702","pleomorphic liposarcoma","umls","C0205825"
> "5702","pleomorphic liposarcoma","mondo","0020562"
> "5703","mixed liposarcoma","umls","C0334472"
> "5703","mixed liposarcoma","mondo","0003594"
> "0110810","hereditary spastic paraplegia 5A","icd10cm","G11.4"
> "0110810","hereditary spastic paraplegia 5A","mondo","0010047"
> "0110811","hereditary spastic paraplegia 6","icd10cm","G11.4"
> "0110811","hereditary spastic paraplegia 6","mondo","0010878"
> "12451","sulfhemoglobinemia","mesh","D013436"
> "12451","sulfhemoglobinemia","umls","C0038732"
> "12451","sulfhemoglobinemia","mondo","0006988"
3543,3617c8247,8255
< "9765","emphysematous cholecystitis","mesh","D041882"
< "9765","emphysematous cholecystitis","umls","C0521610"
< "9765","emphysematous cholecystitis","mondo","0005742"
< "14711","FG syndrome","mesh","C537923"
< "14711","FG syndrome","umls","C0220769"
< "14711","FG syndrome","mondo","0002010"
< "11701","selective IgA deficiency disease","mesh","D017098"
< "11701","selective IgA deficiency disease","umls","C0162538"
< "11701","selective IgA deficiency disease","mondo","0001341"
< "9267","urea cycle disorder","icd10cm","E72.2"
< "9267","urea cycle disorder","icd10cm","E72.20"
< "9267","urea cycle disorder","icd9cm","270.6"
< "9267","urea cycle disorder","mesh","D056806"
< "9267","urea cycle disorder","umls","C0154246"
< "9267","urea cycle disorder","mondo","0004739"
< "0111071","congenital bile acid synthesis defect 1","mesh","C535442"
< "0111071","congenital bile acid synthesis defect 1","umls","C1843116"
< "0111071","congenital bile acid synthesis defect 1","mondo","0011906"
< "5810","adenosine deaminase deficiency","icd10cm","D81.3"
< "5810","adenosine deaminase deficiency","umls","C0268124"
< "5810","adenosine deaminase deficiency","mondo","0007064"
< "5813","purine nucleoside phosphorylase deficiency","icd10cm","D81.5"
< "5813","purine nucleoside phosphorylase deficiency","mesh","C562587"
< "5813","purine nucleoside phosphorylase deficiency","umls","C0268125"
< "5813","purine nucleoside phosphorylase deficiency","mondo","0013171"
< "5815","cerebral lymphoma","umls","C0240803"
< "5815","cerebral lymphoma","mondo","0003655"
< "0060863","patterned macular dystrophy","icd10cm","H35.5"
< "0060863","patterned macular dystrophy","mondo","0020381"
< "0060862","mal de Meleda","icd10cm","Q82.8"
< "0060862","mal de Meleda","mondo","0009552"
< "0060861","microphthalmia with limb anomalies","icd10cm","Q87.2"
< "0060861","microphthalmia with limb anomalies","mondo","0008800"
< "0050709","early infantile epileptic encephalopathy","mondo","0016021"
< "0060866","patterned macular dystrophy 1","mondo","0008210"
< "0060865","patterned macular dystrophy 3","mondo","0014920"
< "0060864","patterned macular dystrophy 2","mondo","0012162"
< "0060869","late-onset retinal degeneration","mondo","0011579"
< "0060868","leukoencephalopathy with vanishing white matter","icd10cm","E75.2"
< "0060868","leukoencephalopathy with vanishing white matter","mondo","0011380"
< "0050700","cardiomyopathy","icd10cm","I42"
< "0050700","cardiomyopathy","icd10cm","I42.9"
< "0050700","cardiomyopathy","icd10cm","I51.5"
< "0050700","cardiomyopathy","icd9cm","425"
< "0050700","cardiomyopathy","icd9cm","425.9"
< "0050700","cardiomyopathy","mesh","D009202"
< "0050700","cardiomyopathy","umls","C0033141"
< "0050700","cardiomyopathy","umls","C0036529"
< "0050700","cardiomyopathy","umls","C0878544"
< "0050700","cardiomyopathy","mondo","0004994"
< "0080119","mitochondrial DNA depletion syndrome 1","mesh","C536350"
< "0080119","mitochondrial DNA depletion syndrome 1","mondo","0011283"
< "12053","cryptococcosis","icd10cm","B45"
< "12053","cryptococcosis","icd10cm","B45.9"
< "12053","cryptococcosis","icd9cm","117.5"
< "12053","cryptococcosis","mesh","D003453"
< "12053","cryptococcosis","umls","C0010414"
< "12053","cryptococcosis","mondo","0005724"
< "0110817","hereditary spastic paraplegia 72","icd10cm","G11.4"
< "0110817","hereditary spastic paraplegia 72","mondo","0014282"
< "234","colon adenocarcinoma","umls","C0338106"
< "234","colon adenocarcinoma","mondo","0002271"
< "4610","intestinal benign neoplasm","mesh","D007414"
< "4610","intestinal benign neoplasm","umls","C0021841"
< "4610","intestinal benign neoplasm","mondo","0021118"
< "230","lateral sclerosis","icd10cm","G12.23"
< "230","lateral sclerosis","icd9cm","335.24"
< "230","lateral sclerosis","mesh","D016472"
< "230","lateral sclerosis","umls","C0154682"
< "230","lateral sclerosis","mondo","0018155"
< "2945","severe acute respiratory syndrome","icd10cm","J12.81"
< "2945","severe acute respiratory syndrome","icd9cm","079.82"
< "2945","severe acute respiratory syndrome","mesh","D045169"
< "2945","severe acute respiratory syndrome","umls","C1175175"
< "2945","severe acute respiratory syndrome","mondo","0005091"
---
> "14019","Brucella canis brucellosis","icd10cm","A23.3"
> "14019","Brucella canis brucellosis","icd9cm","023.3"
> "14019","Brucella canis brucellosis","umls","C0494040"
> "14019","Brucella canis brucellosis","mondo","0001857"
> "14018","alcoholic liver cirrhosis","icd10cm","K70.3"
> "14018","alcoholic liver cirrhosis","icd9cm","571.2"
> "14018","alcoholic liver cirrhosis","mesh","D008104"
> "14018","alcoholic liver cirrhosis","umls","C0023891"
> "14018","alcoholic liver cirrhosis","mondo","0006644"
3623,3660c8261,8274
< "4731","atrophic rhinitis","mesh","D012222"
< "4731","atrophic rhinitis","umls","C0035459"
< "4731","atrophic rhinitis","mondo","0005659"
< "0111019","cone-rod dystrophy 12","mondo","0012983"
< "0111018","cone-rod dystrophy 11","mondo","0012483"
< "2228","thrombocytosis","mesh","D013922"
< "2228","thrombocytosis","umls","C0836924"
< "2228","thrombocytosis","mondo","0002249"
< "2226","myeloproliferative neoplasm","icd10cm","D47.1"
< "2226","myeloproliferative neoplasm","umls","C1292778"
< "2226","myeloproliferative neoplasm","mondo","0020076"
< "0111014","cone-rod dystrophy 8","mondo","0011564"
< "2224","essential thrombocythemia","icd10cm","D47.3"
< "2224","essential thrombocythemia","icd9cm","238.71"
< "2224","essential thrombocythemia","mesh","D013920"
< "2224","essential thrombocythemia","umls","C0040028"
< "2224","essential thrombocythemia","mondo","0005029"
< "0111016","cone-rod dystrophy 13","mondo","0011987"
< "0111011","cone-rod dystrophy 6","mondo","0011143"
< "0111010","cone-rod dystrophy 5","mondo","0010969"
< "0111013","cone-rod dystrophy 3","mondo","0011395"
< "0111012","cone-rod dystrophy 7","mondo","0011355"
< "5146","appendix leiomyoma","umls","C1332327"
< "5146","appendix leiomyoma","mondo","0003300"
< "0110843","xeroderma pigmentosum group A","icd10cm","Q82.1"
< "0110843","xeroderma pigmentosum group A","mondo","0010210"
< "0110723","neuronal ceroid lipofuscinosis 8","icd10cm","E75.4"
< "0110723","neuronal ceroid lipofuscinosis 8","mondo","0010830"
< "4837","Gorham's disease","mesh","D010015"
< "4837","Gorham's disease","umls","C0029436"
< "4837","Gorham's disease","mondo","0003157"
< "1099","alpha thalassemia","icd10cm","D56.0"
< "1099","alpha thalassemia","icd9cm","282.43"
< "1099","alpha thalassemia","mesh","D017085"
< "1099","alpha thalassemia","umls","C0002312"
< "1099","alpha thalassemia","mondo","0011399"
< "0090123","aromatic L-amino acid decarboxylase deficiency","umls","C1291564"
< "0090123","aromatic L-amino acid decarboxylase deficiency","mondo","0012084"
---
> "12698","gynecomastia","icd10cm","N62"
> "12698","gynecomastia","mesh","D006177"
> "12698","gynecomastia","umls","C0018418"
> "12698","gynecomastia","mondo","0001571"
> "10835","chylocele of tunica vaginalis","icd9cm","608.84"
> "10835","chylocele of tunica vaginalis","umls","C0156315"
> "10835","chylocele of tunica vaginalis","mondo","0001136"
> "10834","voyeurism","icd10cm","F65.3"
> "10834","voyeurism","icd9cm","302.82"
> "10834","voyeurism","mesh","D014843"
> "10834","voyeurism","umls","C0042979"
> "10834","voyeurism","mondo","0001135"
> "0110814","hereditary spastic paraplegia 63","icd10cm","G11.4"
> "0110814","hereditary spastic paraplegia 63","mondo","0014305"
3671,3739c8285,8328
< "5143","large bowel leiomyoma","umls","C1333113"
< "5143","large bowel leiomyoma","mondo","0003299"
< "4505","pediatric angiosarcoma","umls","C0279988"
< "4505","pediatric angiosarcoma","mondo","0003022"
< "4504","central nervous system angiosarcoma","umls","C1332875"
< "4504","central nervous system angiosarcoma","mondo","0003021"
< "13477","balanitis xerotica obliterans","icd9cm","607.81"
< "13477","balanitis xerotica obliterans","mesh","D052798"
< "13477","balanitis xerotica obliterans","umls","C0152460"
< "13477","balanitis xerotica obliterans","mondo","0001725"
< "4501","orofaciodigital syndrome","mesh","D009958"
< "4501","orofaciodigital syndrome","umls","C0029294"
< "4501","orofaciodigital syndrome","mondo","0015375"
< "0110724","neuronal ceroid lipofuscinosis 8 northern epilepsy variant","icd10cm","E75.4"
< "0110724","neuronal ceroid lipofuscinosis 8 northern epilepsy variant","mondo","0012391"
< "12357","viral labyrinthitis","icd9cm","386.35"
< "12357","viral labyrinthitis","umls","C0155508"
< "12357","viral labyrinthitis","mondo","0001507"
< "0110585","autosomal dominant nonsyndromic deafness 64","icd10cm","H90.3"
< "0110585","autosomal dominant nonsyndromic deafness 64","mondo","0013593"
< "120","female reproductive organ cancer","icd10cm","C57"
< "120","female reproductive organ cancer","icd9cm","184"
< "120","female reproductive organ cancer","mesh","D005833"
< "120","female reproductive organ cancer","umls","C0017416"
< "120","female reproductive organ cancer","umls","C0153585"
< "120","female reproductive organ cancer","umls","C0699889"
< "120","female reproductive organ cancer","mondo","0001416"
< "0080316","megalencephalic leukoencephalopathy with subcortical cysts 1","umls","C1858854"
< "0080316","megalencephalic leukoencephalopathy with subcortical cysts 1","mondo","0024555"
< "0080315","megalencephalic leukoencephalopathy with subcortical cysts","mesh","C536141"
< "0080315","megalencephalic leukoencephalopathy with subcortical cysts","mondo","0011391"
< "0111169","subcortical band heterotopia","mesh","D054221"
< "0111169","subcortical band heterotopia","umls","C1848201"
< "0111169","subcortical band heterotopia","mondo","0020491"
< "0111168","sepiapterin reductase deficiency","mesh","C562657"
< "0111168","sepiapterin reductase deficiency","umls","C0268468"
< "0111168","sepiapterin reductase deficiency","mondo","0012994"
< "0110725","neuronal ceroid lipofuscinosis 10","icd10cm","E75.4"
< "0110725","neuronal ceroid lipofuscinosis 10","mondo","0012414"
< "1059","intellectual disability","mesh","D008607"
< "1059","intellectual disability","umls","C0025362"
< "1059","intellectual disability","mondo","0001071"
< "0111161","Crouzon syndrome-acanthosis nigricans syndrome","mondo","0012833"
< "0110584","autosomal dominant nonsyndromic deafness 6","icd10cm","H90.3"
< "0110584","autosomal dominant nonsyndromic deafness 6","mondo","0010963"
< "0111163","molybdenum cofactor deficiency type B","mesh","C565373"
< "0111163","molybdenum cofactor deficiency type B","umls","C1854989"
< "0111163","molybdenum cofactor deficiency type B","mondo","0009644"
< "2531","hematologic cancer","mesh","D019337"
< "2531","hematologic cancer","umls","C0376544"
< "2531","hematologic cancer","mondo","0002334"
< "0111165","molybdenum cofactor deficiency","icd10cm","E72.1"
< "0111165","molybdenum cofactor deficiency","mondo","0020480"
< "0111164","molybdenum cofactor deficiency type A","mesh","C565372"
< "0111164","molybdenum cofactor deficiency type A","umls","C1854988"
< "0111164","molybdenum cofactor deficiency type A","mondo","0009643"
< "0111167","Dyggve-Melchior-Clausen disease","mondo","0009130"
< "0111166","molybdenum cofactor deficiency type C","mesh","C565374"
< "0111166","molybdenum cofactor deficiency type C","umls","C1854990"
< "0111166","molybdenum cofactor deficiency type C","mondo","0014212"
< "0110698","hypotrichosis 1","mondo","0011549"
< "0110699","hypotrichosis 2","mondo","0007805"
< "3341","osteitis fibrosa","mesh","D010002"
< "3341","osteitis fibrosa","umls","C0029405"
< "3341","osteitis fibrosa","mondo","0005890"
< "0050670","ataxic cerebral palsy","mondo","0000397"
< "127","leiomyoma","mesh","D007889"
< "127","leiomyoma","umls","C0023267"
< "127","leiomyoma","mondo","0001572"
---
> "0111020","cone-rod dystrophy 9","mondo","0013002"
> "0110815","hereditary spastic paraplegia 64","icd10cm","G11.4"
> "0110815","hereditary spastic paraplegia 64","mondo","0014303"
> "7820","sphenocavernous meningioma","umls","C1336036"
> "7820","sphenocavernous meningioma","mondo","0004370"
> "7827","adult extraosseous osteosarcoma","umls","C0278985"
> "7827","adult extraosseous osteosarcoma","mondo","0004374"
> "7826","adult papillary meningioma","umls","C0281334"
> "7826","adult papillary meningioma","mondo","0004373"
> "7825","chronic toxic polyneuropathy","umls","C1333048"
> "7825","chronic toxic polyneuropathy","mondo","0004372"
> "7824","spinal multifocal clear cell meningioma","umls","C1336051"
> "7824","spinal multifocal clear cell meningioma","mondo","0004371"
> "0080317","megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation","umls","C3150141"
> "0080317","megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation","umls","C3150142"
> "0080317","megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation","umls","C3151356"
> "0080317","megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation","mondo","0013491"
> "1056","oculocerebrorenal syndrome","icd10cm","E72.03"
> "1056","oculocerebrorenal syndrome","mesh","D009800"
> "1056","oculocerebrorenal syndrome","umls","C0028860"
> "1056","oculocerebrorenal syndrome","mondo","0010645"
> "0080314","cone-rod dystrophy 14","mesh","C566579"
> "0080314","cone-rod dystrophy 14","umls","C1838190"
> "0080314","cone-rod dystrophy 14","umls","C1865869"
> "0080314","cone-rod dystrophy 14","umls","C2677463"
> "0080314","cone-rod dystrophy 14","mondo","0011193"
> "3405","histiocytosis","mesh","D015614"
> "3405","histiocytosis","umls","C0019618"
> "3405","histiocytosis","mondo","0002637"
> "0080311","X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance","mondo","0010337"
> "9368","keratoconjunctivitis","icd10cm","H16.2"
> "9368","keratoconjunctivitis","icd10cm","H16.20"
> "9368","keratoconjunctivitis","icd9cm","370.40"
> "9368","keratoconjunctivitis","mesh","D007637"
> "9368","keratoconjunctivitis","umls","C0022573"
> "9368","keratoconjunctivitis","mondo","0004768"
> "9369","orbital plasma cell granuloma","icd10cm","H05.11"
> "9369","orbital plasma cell granuloma","mesh","D016727"
> "9369","orbital plasma cell granuloma","umls","C0085270"
> "9369","orbital plasma cell granuloma","mondo","0004769"
> "9365","vesiculitis","icd10cm","N49.0"
> "9365","vesiculitis","icd9cm","608.0"
> "9365","vesiculitis","umls","C0042588"
> "9365","vesiculitis","mondo","0004767"
3744,3788c8333,8342
< "0050678","Blau syndrome","mondo","0008523"
< "7071","spinal cord dermoid cyst","umls","C1333278"
< "7071","spinal cord dermoid cyst","mondo","0004096"
< "7221","gallbladder papillary carcinoma","umls","C1333753"
< "7221","gallbladder papillary carcinoma","mondo","0004148"
< "7223","breast giant fibroadenoma","umls","C0346157"
< "7223","breast giant fibroadenoma","mondo","0004150"
< "0110726","neuronal ceroid lipofuscinosis 2","icd10cm","E75.4"
< "0110726","neuronal ceroid lipofuscinosis 2","mondo","0008769"
< "9169","Wiskott-Aldrich syndrome","icd10cm","D82.0"
< "9169","Wiskott-Aldrich syndrome","icd9cm","279.12"
< "9169","Wiskott-Aldrich syndrome","mesh","D014923"
< "9169","Wiskott-Aldrich syndrome","umls","C0043194"
< "9169","Wiskott-Aldrich syndrome","mondo","0010518"
< "0070129","autosomal recessive cutis laxa type IID","icd10cm","Q82.8"
< "0070129","autosomal recessive cutis laxa type IID","mondo","0027451"
< "0070128","congenital nongoitrous hypothyroidism 6","icd10cm","E03.1"
< "0070128","congenital nongoitrous hypothyroidism 6","mondo","0013757"
< "10691","fat necrosis of breast","icd10cm","N64.1"
< "10691","fat necrosis of breast","icd9cm","611.3"
< "10691","fat necrosis of breast","umls","C0156321"
< "10691","fat necrosis of breast","mondo","0001101"
< "0070126","congenital nongoitrous hypothyroidism 1","icd10cm","E03.1"
< "0070126","congenital nongoitrous hypothyroidism 1","mondo","0010142"
< "0070125","congenital nongoitrous hypothyroidism 5","icd10cm","E03.1"
< "0070125","congenital nongoitrous hypothyroidism 5","mondo","0009154"
< "0070124","congenital nongoitrous hypothyroidism 2","icd10cm","E03.1"
< "0070124","congenital nongoitrous hypothyroidism 2","mondo","0024264"
< "0070123","congenital nongoitrous hypothyroidism 4","icd10cm","E03.1"
< "0070123","congenital nongoitrous hypothyroidism 4","mondo","0010139"
< "2671","transitional cell carcinoma","mesh","D002295"
< "2671","transitional cell carcinoma","umls","C0007138"
< "2671","transitional cell carcinoma","umls","C0334265"
< "2671","transitional cell carcinoma","mondo","0006474"
< "0070121","Meckel syndrome 7","mesh","C537756"
< "0070121","Meckel syndrome 7","umls","C2673885"
< "0070121","Meckel syndrome 7","mondo","0009966"
< "0070120","Meckel syndrome 6","icd10cm","Q61.9"
< "0070120","Meckel syndrome 6","mondo","0012848"
< "0110265","cataract 31 multiple types","icd10cm","Q12.0"
< "0110265","cataract 31 multiple types","mondo","0011547"
< "0110168","Charcot-Marie-Tooth disease type 2Y","icd10cm","G60.0"
< "0110168","Charcot-Marie-Tooth disease type 2Y","mondo","0014735"
< "0110169","Charcot-Marie-Tooth disease axonal type 2P","icd10cm","G60.0"
< "0110169","Charcot-Marie-Tooth disease axonal type 2P","mondo","0013753"
---
> "9360","intrinsic asthma","icd10cm","J45"
> "9360","intrinsic asthma","icd9cm","493.1"
> "9360","intrinsic asthma","umls","C0155880"
> "9360","intrinsic asthma","mondo","0004765"
> "8986","narcolepsy","icd10cm","G47.41"
> "8986","narcolepsy","icd10cm","G47.419"
> "8986","narcolepsy","icd9cm","347.0"
> "8986","narcolepsy","mesh","D009290"
> "8986","narcolepsy","umls","C0027404"
> "8986","narcolepsy","mondo","0021107"
3794,3813c8348,8355
< "0110264","cataract 33","icd10cm","Q12.0"
< "0110264","cataract 33","mondo","0012665"
< "0110162","Charcot-Marie-Tooth disease, axonal type 2W","mondo","0014711"
< "10686","lactocele","icd10cm","N64.89"
< "10686","lactocele","icd9cm","611.5"
< "10686","lactocele","mesh","C535998"
< "10686","lactocele","umls","C0152243"
< "10686","lactocele","mondo","0001099"
< "0110160","Charcot-Marie-Tooth disease axonal type 2T","icd10cm","G60.0"
< "0110160","Charcot-Marie-Tooth disease axonal type 2T","mondo","0014866"
< "0110161","Charcot-Marie-Tooth disease type 2R","icd10cm","G60.0"
< "0110161","Charcot-Marie-Tooth disease type 2R","mondo","0014208"
< "0110166","Charcot-Marie-Tooth disease axonal type 2H","icd10cm","G60.0"
< "0110166","Charcot-Marie-Tooth disease axonal type 2H","mondo","0011901"
< "0110167","Charcot-Marie-Tooth disease axonal type 2K","icd10cm","G60.0"
< "0110167","Charcot-Marie-Tooth disease axonal type 2K","mondo","0011916"
< "0110164","Charcot-Marie-Tooth disease type 2D","icd10cm","G60.0"
< "0110164","Charcot-Marie-Tooth disease type 2D","mondo","0011091"
< "0110165","Charcot-Marie-Tooth disease type 2E","icd10cm","G60.0"
< "0110165","Charcot-Marie-Tooth disease type 2E","mondo","0011894"
---
> "1835","mononeuritis multiplex","icd10cm","G58.7"
> "1835","mononeuritis multiplex","icd9cm","354.5"
> "1835","mononeuritis multiplex","mesh","D020422"
> "1835","mononeuritis multiplex","umls","C0151295"
> "1835","mononeuritis multiplex","mondo","0002128"
> "1838","Menkes disease","mesh","D007706"
> "1838","Menkes disease","umls","C0022716"
> "1838","Menkes disease","mondo","0010651"
3818a8361,8363
> "2155","malignant ovarian germ cell neoplasm","mesh","C562841"
> "2155","malignant ovarian germ cell neoplasm","umls","C0346180"
> "2155","malignant ovarian germ cell neoplasm","mondo","0018171"
3821,3830c8366,8369
< "9563","bronchiectasis","icd10cm","J47"
< "9563","bronchiectasis","icd10cm","J47.9"
< "9563","bronchiectasis","icd9cm","494"
< "9563","bronchiectasis","mesh","D001987"
< "9563","bronchiectasis","umls","C0006267"
< "9563","bronchiectasis","mondo","0004822"
< "0110768","hereditary spastic paraplegia 15","icd10cm","G11.4"
< "0110768","hereditary spastic paraplegia 15","mondo","0010044"
< "0110769","hereditary spastic paraplegia 16","icd10cm","G11.4"
< "0110769","hereditary spastic paraplegia 16","mondo","0010287"
---
> "4985","extraosseous Ewings sarcoma-primitive neuroepithelial tumor","umls","C0279980"
> "4985","extraosseous Ewings sarcoma-primitive neuroepithelial tumor","mondo","0021039"
> "2151","malignant ovarian surface epithelial-stromal neoplasm","umls","C1518236"
> "2151","malignant ovarian surface epithelial-stromal neoplasm","mondo","0018364"
3838,3861c8377,8389
< "0110764","hereditary spastic paraplegia 11","icd10cm","G11.4"
< "0110764","hereditary spastic paraplegia 11","mondo","0011445"
< "0110765","hereditary spastic paraplegia 12","icd10cm","G11.4"
< "0110765","hereditary spastic paraplegia 12","mondo","0011489"
< "0110766","hereditary spastic paraplegia 13","icd10cm","G11.4"
< "0110766","hereditary spastic paraplegia 13","mondo","0011532"
< "0110767","hereditary spastic paraplegia 14","icd10cm","G11.4"
< "0110767","hereditary spastic paraplegia 14","mondo","0011522"
< "0110760","type 1 diabetes mellitus 23","icd10cm","E10"
< "0110760","type 1 diabetes mellitus 23","mondo","0012961"
< "0110761","type 1 diabetes mellitus 24","icd10cm","E10"
< "0110761","type 1 diabetes mellitus 24","mondo","0013078"
< "934","viral infectious disease","icd10cm","A94"
< "934","viral infectious disease","icd10cm","B34"
< "934","viral infectious disease","icd10cm","B34.9"
< "934","viral infectious disease","icd9cm","060-066.99"
< "934","viral infectious disease","icd9cm","066.9"
< "934","viral infectious disease","mesh","D001102"
< "934","viral infectious disease","mesh","D014777"
< "934","viral infectious disease","umls","C0003723"
< "934","viral infectious disease","umls","C0042769"
< "934","viral infectious disease","mondo","0005108"
< "0110184","Charcot-Marie-Tooth disease type 4J","icd10cm","G60.0"
< "0110184","Charcot-Marie-Tooth disease type 4J","mondo","0012640"
---
> "4989","pancreatitis","icd10cm","K85.9"
> "4989","pancreatitis","mesh","D010195"
> "4989","pancreatitis","umls","C0030305"
> "4989","pancreatitis","mondo","0004982"
> "4988","alcoholic pancreatitis","mesh","D019512"
> "4988","alcoholic pancreatitis","umls","C0376670"
> "4988","alcoholic pancreatitis","mondo","0003232"
> "2409","rhinosporidiosis","icd10cm","B48.1"
> "2409","rhinosporidiosis","icd9cm","117.0"
> "2409","rhinosporidiosis","mesh","D012227"
> "2409","rhinosporidiosis","umls","C0035469"
> "2409","rhinosporidiosis","mondo","0005946"
> "0080043","achondrogenesis","mondo","0019648"
3864,3865c8392,8393
< "5382","Bartholin's gland adenoma","umls","C1511048"
< "5382","Bartholin's gland adenoma","mondo","0003419"
---
> "0110186","Charcot-Marie-Tooth disease type 4D","icd10cm","G60.0"
> "0110186","Charcot-Marie-Tooth disease type 4D","mondo","0011085"
3874,3882d8401
< "11836","clubfoot","icd10cm","Q66.0"
< "11836","clubfoot","icd10cm","Q66.89"
< "11836","clubfoot","icd9cm","754.51"
< "11836","clubfoot","mesh","D003025"
< "11836","clubfoot","umls","C0009081"
< "11836","clubfoot","mondo","0007342"
< "0060312","angular cheilitis","icd10cm","K13.0"
< "0060312","angular cheilitis","umls","C0221237"
< "0060312","angular cheilitis","mondo","0000741"
3887,3893d8405
< "11830","myopia","icd10cm","H52.1"
< "11830","myopia","icd9cm","367.1"
< "11830","myopia","mesh","D009216"
< "11830","myopia","umls","C0027092"
< "11830","myopia","mondo","0001384"
< "4876","trachea carcinoma","umls","C0848879"
< "4876","trachea carcinoma","mondo","0003184"
3901a8414,8415
> "14066","acute diffuse nephritis","umls","C0341689"
> "14066","acute diffuse nephritis","mondo","0001871"
3908,3934c8422,8438
< "0080082","nonsyndromic congenital nail disorder 4","mesh","C536377"
< "0080082","nonsyndromic congenital nail disorder 4","mondo","0008798"
< "0070239","primary coenzyme Q10 deficiency 2","mondo","0013837"
< "0070238","primary coenzyme Q10 deficiency 1","mondo","0011829"
< "13099","Moyamoya disease","icd10cm","I67.5"
< "13099","Moyamoya disease","icd9cm","437.5"
< "13099","Moyamoya disease","mesh","D009072"
< "13099","Moyamoya disease","umls","C0026654"
< "13099","Moyamoya disease","mondo","0016820"
< "0070233","Loeys-Dietz syndrome 4","mondo","0013897"
< "0070232","benign recurrent intrahepatic cholestasis 2","umls","C2608083"
< "0070232","benign recurrent intrahepatic cholestasis 2","umls","C3489789"
< "0070232","benign recurrent intrahepatic cholestasis 2","mondo","0011559"
< "0070231","benign recurrent intrahepatic cholestasis 1","umls","C1855731"
< "0070231","benign recurrent intrahepatic cholestasis 1","mondo","0009469"
< "0070230","benign recurrent intrahepatic cholestasis","umls","C0149841"
< "0070230","benign recurrent intrahepatic cholestasis","mondo","0019008"
< "0070237","Loeys-Dietz syndrome 3","mondo","0013426"
< "0070236","Loeys-Dietz syndrome 5","mondo","0014262"
< "0070235","Loeys-Dietz syndrome 1","mondo","0012212"
< "0070234","Loeys-Dietz syndrome 2","mondo","0012427"
< "0110508","autosomal recessive nonsyndromic deafness 51","icd10cm","H90.3"
< "0110508","autosomal recessive nonsyndromic deafness 51","mondo","0012370"
< "0110509","autosomal recessive nonsyndromic deafness 53","icd10cm","H90.3"
< "0110509","autosomal recessive nonsyndromic deafness 53","mondo","0012333"
< "0090129","carnitine palmitoyltransferase I deficiency","icd10cm","E71.3"
< "0090129","carnitine palmitoyltransferase I deficiency","mondo","0009705"
---
> "14064","acute poststreptococcal glomerulonephritis","umls","C0403414"
> "14064","acute poststreptococcal glomerulonephritis","mondo","0001870"
> "0080042","autosomal recessive spinocerebellar ataxia 18","mondo","0014530"
> "3241","lipid pneumonia","icd10cm","J69.1"
> "3241","lipid pneumonia","mesh","D011017"
> "3241","lipid pneumonia","umls","C0032298"
> "3241","lipid pneumonia","mondo","0005826"
> "3240","aspiration pneumonitis","icd10cm","J69.0"
> "3240","aspiration pneumonitis","mesh","D011015"
> "3240","aspiration pneumonitis","umls","C0032290"
> "3240","aspiration pneumonitis","mondo","0002572"
> "3247","rhabdomyosarcoma","mesh","D012208"
> "3247","rhabdomyosarcoma","umls","C0035412"
> "3247","rhabdomyosarcoma","mondo","0005212"
> "3246","embryonal rhabdomyosarcoma","mesh","D018233"
> "3246","embryonal rhabdomyosarcoma","umls","C0206656"
> "3246","embryonal rhabdomyosarcoma","mondo","0009993"
3941,3966c8445,8468
< "0060216","Cogan syndrome","icd10cm","H16.32"
< "0060216","Cogan syndrome","mesh","D055952"
< "0060216","Cogan syndrome","umls","C0271270"
< "0060216","Cogan syndrome","mondo","0015453"
< "11905","labium majus cancer","icd10cm","C51.0"
< "11905","labium majus cancer","icd9cm","184.1"
< "11905","labium majus cancer","umls","C0496814"
< "11905","labium majus cancer","mondo","0001403"
< "0110500","autosomal recessive nonsyndromic deafness 42","icd10cm","H90.3"
< "0110500","autosomal recessive nonsyndromic deafness 42","mondo","0012326"
< "0110501","autosomal recessive nonsyndromic deafness 44","icd10cm","H90.3"
< "0110501","autosomal recessive nonsyndromic deafness 44","mondo","0012421"
< "0110502","autosomal recessive nonsyndromic deafness 45","icd10cm","H90.3"
< "0110502","autosomal recessive nonsyndromic deafness 45","mondo","0012903"
< "0110503","autosomal recessive nonsyndromic deafness 46","icd10cm","H90.3"
< "0110503","autosomal recessive nonsyndromic deafness 46","mondo","0012327"
< "0110504","autosomal recessive nonsyndromic deafness 47","icd10cm","H90.3"
< "0110504","autosomal recessive nonsyndromic deafness 47","mondo","0012375"
< "12308","Dubin-Johnson syndrome","icd10cm","E80.6"
< "12308","Dubin-Johnson syndrome","mesh","D007566"
< "12308","Dubin-Johnson syndrome","umls","C0022350"
< "12308","Dubin-Johnson syndrome","mondo","0009380"
< "0110506","autosomal recessive nonsyndromic deafness 49","icd10cm","H90.3"
< "0110506","autosomal recessive nonsyndromic deafness 49","mondo","0012420"
< "0110507","autosomal recessive nonsyndromic deafness 5","icd10cm","H90.3"
< "0110507","autosomal recessive nonsyndromic deafness 5","mondo","0000912"
---
> "0111589","COACH syndrome","mesh","C536430"
> "0111589","COACH syndrome","umls","C1857662"
> "0111588","Greenberg dysplasia","mesh","C535858"
> "0111588","Greenberg dysplasia","umls","C2931048"
> "13254","diverticulitis of colon","mesh","D004239"
> "13254","diverticulitis of colon","umls","C0012814"
> "13254","diverticulitis of colon","mondo","0001674"
> "0111586","Martsolf syndrome","mesh","C536028"
> "0111586","Martsolf syndrome","umls","C0796037"
> "0111585","carnitine-acylcarnitine translocase deficiency","mesh","C562812"
> "0111585","carnitine-acylcarnitine translocase deficiency","umls","C0342791"
> "0111584","dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","mesh","C535580"
> "0111584","dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","mesh","C535703"
> "0111584","dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","umls","C0796031"
> "0111584","dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","umls","C0796083"
> "13250","diarrhea","icd9cm","009.2"
> "13250","diarrhea","mesh","D003967"
> "13250","diarrhea","umls","C0013369"
> "13250","diarrhea","mondo","0001673"
> "13252","mesenteric vascular occlusion","mesh","D008641"
> "13252","mesenteric vascular occlusion","umls","C0025472"
> "13252","mesenteric vascular occlusion","mondo","0006855"
> "0111580","Behr syndrome","mesh","C537669"
> "0111580","Behr syndrome","umls","C0221061"
3972a8475,8476
> "0110237","cataract 42","icd10cm","Q12.0"
> "0110237","cataract 42","mondo","0007283"
3985,3997c8489,8491
< "7031","glottis squamous cell carcinoma","umls","C0280325"
< "7031","glottis squamous cell carcinoma","mondo","0004080"
< "7032","bile duct clear cell adenocarcinoma","umls","C0861855"
< "7032","bile duct clear cell adenocarcinoma","mondo","0004081"
< "7033","anisakiasis","icd10cm","B81.0"
< "7033","anisakiasis","icd9cm","127.1"
< "7033","anisakiasis","mesh","D017129"
< "7033","anisakiasis","umls","C0162576"
< "7033","anisakiasis","mondo","0015200"
< "9011","larynx carcinoma in situ","icd10cm","D02.0"
< "9011","larynx carcinoma in situ","icd9cm","231.0"
< "9011","larynx carcinoma in situ","umls","C0154069"
< "9011","larynx carcinoma in situ","mondo","0004696"
---
> "1483","gingival disease","mesh","D005882"
> "1483","gingival disease","umls","C0017563"
> "1483","gingival disease","mondo","0002021"
4002,4003c8496,8498
< "7037","childhood immature teratoma of ovary","umls","C1332990"
< "7037","childhood immature teratoma of ovary","mondo","0004082"
---
> "3309","neurodermatitis","mesh","D009450"
> "3309","neurodermatitis","umls","C0027822"
> "3309","neurodermatitis","mondo","0006585"
4005a8501,8505
> "5495","monophasic synovial sarcoma","umls","C1334801"
> "5495","monophasic synovial sarcoma","mondo","0005067"
> "3304","germinoma","mesh","D018237"
> "3304","germinoma","umls","C0206660"
> "3304","germinoma","mondo","0002598"
4012,4169c8512,8576
< "1712","aortic valve stenosis","mesh","D001024"
< "1712","aortic valve stenosis","umls","C0003507"
< "1712","aortic valve stenosis","umls","C0152417"
< "1712","aortic valve stenosis","umls","C0155567"
< "1712","aortic valve stenosis","mondo","0004978"
< "0060308","autosomal recessive non-syndromic intellectual disability","mondo","0019502"
< "0060309","syndromic X-linked intellectual disability","mondo","0020119"
< "5254","central nervous system leiomyosarcoma","umls","C1334385"
< "5254","central nervous system leiomyosarcoma","mondo","0003349"
< "2146","ovary sarcoma","umls","C0280746"
< "2146","ovary sarcoma","mondo","0002225"
< "5259","colon leiomyosarcoma","umls","C1333093"
< "5259","colon leiomyosarcoma","mondo","0003351"
< "0060306","Meier-Gorlin syndrome","mesh","C538012"
< "0060306","Meier-Gorlin syndrome","umls","C1868684"
< "0060306","Meier-Gorlin syndrome","mondo","0016817"
< "0060307","autosomal dominant non-syndromic intellectual disability","mondo","0015802"
< "799","varicose veins","icd10cm","I83.90"
< "799","varicose veins","mesh","D014648"
< "799","varicose veins","umls","C0042345"
< "799","varicose veins","mondo","0008638"
< "0060305","megalocornea","mesh","C562829"
< "0060305","megalocornea","umls","C0344530"
< "0060305","megalocornea","mondo","0009576"
< "0110342","osteogenesis imperfecta type 13","icd10cm","Q78.0"
< "0110342","osteogenesis imperfecta type 13","mondo","0013924"
< "0110343","osteogenesis imperfecta type 14","icd10cm","Q78.0"
< "0110343","osteogenesis imperfecta type 14","mondo","0014029"
< "0110436","dilated cardiomyopathy 1L","icd10cm","I42.0"
< "0110436","dilated cardiomyopathy 1L","mondo","0011702"
< "0110341","osteogenesis imperfecta type 2","icd10cm","Q78.0"
< "0110341","osteogenesis imperfecta type 2","mondo","0008147"
< "0110430","dilated cardiomyopathy 1G","icd10cm","I42.0"
< "0110430","dilated cardiomyopathy 1G","mondo","0011400"
< "0110347","osteogenesis imperfecta type 15","icd10cm","Q78.0"
< "0110347","osteogenesis imperfecta type 15","mondo","0014086"
< "0110344","osteogenesis imperfecta type 5","icd10cm","Q78.0"
< "0110344","osteogenesis imperfecta type 5","mondo","0012591"
< "0110345","osteogenesis imperfecta type 16","icd10cm","Q78.0"
< "0110345","osteogenesis imperfecta type 16","mondo","0014544"
< "6316","Bartholin's gland adenocarcinoma","umls","C0238016"
< "6316","Bartholin's gland adenocarcinoma","mondo","0003853"
< "0110348","osteogenesis imperfecta type 12","icd10cm","Q78.0"
< "0110348","osteogenesis imperfecta type 12","mondo","0013460"
< "0110349","osteogenesis imperfecta type 9","icd10cm","Q78.0"
< "0110349","osteogenesis imperfecta type 9","mondo","0009805"
< "0110438","dilated cardiomyopathy 1JJ","icd10cm","I42.0"
< "0110438","dilated cardiomyopathy 1JJ","mondo","0014095"
< "0110439","dilated cardiomyopathy 1P","icd10cm","I42.0"
< "0110439","dilated cardiomyopathy 1P","mondo","0012362"
< "0060828","X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome","mondo","0010473"
< "14336","estrogen excess","icd10cm","E28.0"
< "14336","estrogen excess","icd9cm","256.0"
< "14336","estrogen excess","umls","C0154209"
< "14336","estrogen excess","mondo","0001946"
< "0110751","type 1 diabetes mellitus 12","icd10cm","E10"
< "0110751","type 1 diabetes mellitus 12","mondo","0011068"
< "11123","Henoch-Schoenlein purpura","icd10cm","D69.0"
< "11123","Henoch-Schoenlein purpura","icd9cm","287.0"
< "11123","Henoch-Schoenlein purpura","mesh","D011695"
< "11123","Henoch-Schoenlein purpura","umls","C0034152"
< "11123","Henoch-Schoenlein purpura","mondo","0006785"
< "14330","Parkinson's disease","kegg","05012"
< "14330","Parkinson's disease","icd10cm","G20"
< "14330","Parkinson's disease","icd9cm","332"
< "14330","Parkinson's disease","icd9cm","332.0"
< "14330","Parkinson's disease","mesh","D010300"
< "14330","Parkinson's disease","umls","C0030567"
< "14330","Parkinson's disease","mondo","0005180"
< "14447","gonadal dysgenesis","icd9cm","758.6"
< "14447","gonadal dysgenesis","mesh","D006059"
< "14447","gonadal dysgenesis","umls","C0018051"
< "14447","gonadal dysgenesis","mondo","0001967"
< "14448","46 XY gonadal dysgenesis","mesh","D006061"
< "14448","46 XY gonadal dysgenesis","umls","C0018054"
< "14448","46 XY gonadal dysgenesis","mondo","0010765"
< "7787","breast osteosarcoma","umls","C1335149"
< "7787","breast osteosarcoma","mondo","0004360"
< "0111170","autosomal dominant sensory ataxia 1","mondo","0012166"
< "4067","anus sarcoma","umls","C1332277"
< "4067","anus sarcoma","mondo","0002865"
< "14686","Axenfeld-Rieger syndrome","icd10cm","Q13.81"
< "14686","Axenfeld-Rieger syndrome","mesh","C535679"
< "14686","Axenfeld-Rieger syndrome","umls","C0265341"
< "14686","Axenfeld-Rieger syndrome","mondo","0019187"
< "0050880","Koolen de Vries syndrome","mondo","0012496"
< "0050881","inclusion body myopathy with Paget disease of bone and frontotemporal dementia","mondo","0000507"
< "7148","rheumatoid arthritis","kegg","05323"
< "7148","rheumatoid arthritis","icd10cm","M06.9"
< "7148","rheumatoid arthritis","icd9cm","714.0"
< "7148","rheumatoid arthritis","mesh","D001172"
< "7148","rheumatoid arthritis","umls","C0003873"
< "7148","rheumatoid arthritis","mondo","0008383"
< "13775","plantar wart","icd10cm","B07.0"
< "13775","plantar wart","icd9cm","078.12"
< "13775","plantar wart","umls","C0042548"
< "13775","plantar wart","mondo","0001795"
< "0050884","triosephosphate isomerase deficiency","mondo","0014221"
< "0050885","IMAGe syndrome","mondo","0013873"
< "3012","Li-Fraumeni syndrome","mesh","D016864"
< "3012","Li-Fraumeni syndrome","umls","C0085390"
< "3012","Li-Fraumeni syndrome","mondo","0018875"
< "7371","superficial urinary bladder cancer","umls","C1336527"
< "7371","superficial urinary bladder cancer","mondo","0004200"
< "3010","lobular neoplasia","umls","C0861352"
< "3010","lobular neoplasia","mondo","0002486"
< "4143","orbital cancer","icd10cm","C69.6"
< "4143","orbital cancer","icd9cm","190.1"
< "4143","orbital cancer","mesh","D009918"
< "4143","orbital cancer","umls","C0029185"
< "4143","orbital cancer","umls","C0153626"
< "4143","orbital cancer","mondo","0002889"
< "2717","Bloom syndrome","mesh","D001816"
< "2717","Bloom syndrome","umls","C0005859"
< "2717","Bloom syndrome","mondo","0008876"
< "3017","breast sarcoma","umls","C0349667"
< "3017","breast sarcoma","mondo","0002490"
< "10755","petrositis","icd10cm","H70.2"
< "10755","petrositis","icd10cm","H70.20"
< "10755","petrositis","icd10cm","H70.209"
< "10755","petrositis","icd10cm","H70.21"
< "10755","petrositis","icd10cm","H70.219"
< "10755","petrositis","icd10cm","H70.22"
< "10755","petrositis","icd10cm","H70.229"
< "10755","petrositis","icd9cm","383.2"
< "10755","petrositis","icd9cm","383.20"
< "10755","petrositis","icd9cm","383.21"
< "10755","petrositis","icd9cm","383.22"
< "10755","petrositis","mesh","D059270"
< "10755","petrositis","umls","C0155448"
< "10755","petrositis","umls","C0155449"
< "10755","petrositis","umls","C0155450"
< "10755","petrositis","mondo","0001109"
< "8729","milker's nodule","icd10cm","B08.04"
< "8729","milker's nodule","icd9cm","051.1"
< "8729","milker's nodule","icd9cm","051.9"
< "8729","milker's nodule","mesh","D011213"
< "8729","milker's nodule","umls","C0026143"
< "8729","milker's nodule","mondo","0005850"
< "4743","mixed testicular germ cell tumor","umls","C1336720"
< "4743","mixed testicular germ cell tumor","mondo","0003120"
< "0110757","type 1 diabetes mellitus 20","icd10cm","E10"
< "0110757","type 1 diabetes mellitus 20","mondo","0012919"
< "2231","factor XII deficiency","mesh","D005175"
< "2231","factor XII deficiency","umls","C0015526"
< "2231","factor XII deficiency","mondo","0009315"
< "0060786","hypomyelinating leukodystrophy","mondo","0019046"
< "1003","pelvic inflammatory disease","icd10cm","N70-N77"
< "1003","pelvic inflammatory disease","icd10cm","N73.9"
< "1003","pelvic inflammatory disease","icd9cm","614-616.99"
< "1003","pelvic inflammatory disease","icd9cm","614.9"
< "1003","pelvic inflammatory disease","mesh","D000292"
< "1003","pelvic inflammatory disease","umls","C0242172"
< "1003","pelvic inflammatory disease","mondo","0000922"
< "8503","impetigo herpetiformis","icd10cm","L40.1"
< "8503","impetigo herpetiformis","icd9cm","694.3"
< "8503","impetigo herpetiformis","umls","C1314968"
< "8503","impetigo herpetiformis","mondo","0004591"
---
> "3303","notochordal cancer","umls","C1335069"
> "3303","notochordal cancer","mondo","0002597"
> "5492","biphasic synovial sarcoma","umls","C0334507"
> "5492","biphasic synovial sarcoma","mondo","0003468"
> "3301","gonadoblastoma","mesh","D018238"
> "3301","gonadoblastoma","umls","C0206661"
> "3301","gonadoblastoma","mondo","0010768"
> "10611","protein-losing enteropathy","mesh","D011504"
> "10611","protein-losing enteropathy","umls","C0033680"
> "10611","protein-losing enteropathy","mondo","0009174"
> "1270","hereditary hemorrhagic telangiectasia","icd10cm","I78.0"
> "1270","hereditary hemorrhagic telangiectasia","icd9cm","448.0"
> "1270","hereditary hemorrhagic telangiectasia","mesh","D013683"
> "1270","hereditary hemorrhagic telangiectasia","umls","C0039445"
> "1270","hereditary hemorrhagic telangiectasia","mondo","0019180"
> "13499","jejunal cancer","icd10cm","C17.1"
> "13499","jejunal cancer","icd9cm","152.1"
> "13499","jejunal cancer","mesh","D007580"
> "13499","jejunal cancer","umls","C0153427"
> "13499","jejunal cancer","mondo","0006815"
> "12145","detrusor sphincter dyssynergia","icd9cm","596.55"
> "12145","detrusor sphincter dyssynergia","umls","C0341747"
> "12145","detrusor sphincter dyssynergia","mondo","0001447"
> "12144","low compliance bladder","icd9cm","596.52"
> "12144","low compliance bladder","umls","C0489967"
> "12144","low compliance bladder","mondo","0001446"
> "13492","active cochlear Meniere's disease","icd9cm","386.02"
> "13492","active cochlear Meniere's disease","umls","C0155497"
> "13492","active cochlear Meniere's disease","mondo","0001729"
> "0080046","Stickler syndrome","mondo","0019354"
> "13490","active cochleovestibular Meniere's disease","icd9cm","386.01"
> "13490","active cochleovestibular Meniere's disease","umls","C0155496"
> "13490","active cochleovestibular Meniere's disease","mondo","0001727"
> "0111391","mucopolysaccharidosis IVA","icd10cm","E76.210"
> "0111391","mucopolysaccharidosis IVA","umls","C0086651"
> "13491","active vestibular Meniere's disease","icd9cm","386.03"
> "13491","active vestibular Meniere's disease","umls","C0155498"
> "13491","active vestibular Meniere's disease","mondo","0001728"
> "0111217","autosomal dominant centronuclear myopathy","umls","C1834558"
> "2065","syringoma","mesh","D018252"
> "2065","syringoma","umls","C0206673"
> "2065","syringoma","mondo","0002191"
> "519","aortitis","icd10cm","I77.6"
> "519","aortitis","mesh","D001025"
> "519","aortitis","umls","C0003509"
> "519","aortitis","mondo","0006656"
> "518","scrotum neoplasm","icd10cm","C63.2"
> "518","scrotum neoplasm","icd9cm","187.7"
> "518","scrotum neoplasm","umls","C0153604"
> "518","scrotum neoplasm","umls","C0341790"
> "518","scrotum neoplasm","mondo","0003319"
> "0080045","Kniest dysplasia","mesh","C537207"
> "0080045","Kniest dysplasia","mondo","0007987"
> "512","epididymal neoplasm","umls","C0346239"
> "512","epididymal neoplasm","mondo","0003283"
> "1227","neutropenia","icd10cm","D70"
> "1227","neutropenia","icd10cm","D70.9"
> "1227","neutropenia","icd9cm","288.0"
> "1227","neutropenia","icd9cm","288.00"
> "1227","neutropenia","mesh","D009503"
> "1227","neutropenia","umls","C0027947"
> "1227","neutropenia","mondo","0001475"
> "620","blood protein disease","mesh","D001796"
> "620","blood protein disease","umls","C0005830"
> "620","blood protein disease","mondo","0003804"
4177,4183c8584,8588
< "8506","bullous pemphigoid","icd10cm","L12"
< "8506","bullous pemphigoid","icd10cm","L12.0"
< "8506","bullous pemphigoid","icd10cm","L12.9"
< "8506","bullous pemphigoid","icd9cm","694.5"
< "8506","bullous pemphigoid","mesh","D010391"
< "8506","bullous pemphigoid","umls","C0030805"
< "8506","bullous pemphigoid","mondo","0019082"
---
> "625","transient hypogammaglobulinemia","umls","C0859960"
> "625","transient hypogammaglobulinemia","mondo","0003827"
> "624","transient hypogammaglobulinemia of infancy","icd10cm","D80.7"
> "624","transient hypogammaglobulinemia of infancy","umls","C0272238"
> "624","transient hypogammaglobulinemia of infancy","mondo","0015698"
4197,4203c8602,8608
< "4186","articulation disorder","mesh","D001184"
< "4186","articulation disorder","umls","C0003910"
< "4186","articulation disorder","mondo","0002903"
< "5662","pleomorphic carcinoma","umls","C0334233"
< "5662","pleomorphic carcinoma","mondo","0003573"
< "5660","lymphoepithelioma-like carcinoma","umls","C0334254"
< "5660","lymphoepithelioma-like carcinoma","mondo","0003572"
---
> "6536","plasma cell neoplasm","mesh","D010265"
> "6536","plasma cell neoplasm","umls","C1136084"
> "6536","plasma cell neoplasm","mondo","0004959"
> "0080044","hypochondrogenesis","mesh","C563007"
> "0080044","hypochondrogenesis","mondo","0019669"
> "8292","atypical follicular adenoma","umls","C1266046"
> "8292","atypical follicular adenoma","mondo","0004524"
4209,4246c8614,8635
< "2883","prostatic adenoma","mesh","D011470"
< "2883","prostatic adenoma","umls","C0520477"
< "2883","prostatic adenoma","mondo","0002450"
< "5538","external ear squamous cell carcinoma","umls","C1333494"
< "5538","external ear squamous cell carcinoma","mondo","0003501"
< "2887","prostate leiomyoma","umls","C1335510"
< "2887","prostate leiomyoma","mondo","0002452"
< "0060055","popliteal pterygium syndrome","mesh","C562509"
< "0060055","popliteal pterygium syndrome","umls","C0265259"
< "0060055","popliteal pterygium syndrome","mondo","0017435"
< "0060058","lymphoma","icd10cm","C85.9"
< "0060058","lymphoma","mesh","D008223"
< "0060058","lymphoma","umls","C0024299"
< "0060058","lymphoma","umls","C0598798"
< "0060058","lymphoma","mondo","0005062"
< "2678","adult mesoblastic nephroma","umls","C1272677"
< "2678","adult mesoblastic nephroma","mondo","0002386"
< "7497","brain ependymoma","umls","C0238029"
< "7497","brain ependymoma","mondo","0004245"
< "0110031","hemoglobin H disease","icd10cm","D56.0"
< "0110031","hemoglobin H disease","mondo","0013512"
< "8619","recurrent hypersomnia","icd10cm","G47.13"
< "8619","recurrent hypersomnia","icd9cm","327.13"
< "8619","recurrent hypersomnia","mesh","D006970"
< "8619","recurrent hypersomnia","umls","C0751226"
< "8619","recurrent hypersomnia","mondo","0004617"
< "8618","oral cavity cancer","icd10cm","C04"
< "8618","oral cavity cancer","icd10cm","C04.0"
< "8618","oral cavity cancer","icd10cm","C04.1"
< "8618","oral cavity cancer","icd10cm","C04.9"
< "8618","oral cavity cancer","icd9cm","144"
< "8618","oral cavity cancer","icd9cm","144.0"
< "8618","oral cavity cancer","icd9cm","144.1"
< "8618","oral cavity cancer","icd9cm","144.9"
< "8618","oral cavity cancer","umls","C0153368"
< "8618","oral cavity cancer","umls","C0153369"
< "8618","oral cavity cancer","umls","C0496758"
< "8618","oral cavity cancer","mondo","0005515"
---
> "6530","cortical thymoma","umls","C1266095"
> "6530","cortical thymoma","mondo","0003915"
> "8791","breast carcinoma in situ","icd10cm","D05"
> "8791","breast carcinoma in situ","icd10cm","D05.9"
> "8791","breast carcinoma in situ","icd9cm","233.0"
> "8791","breast carcinoma in situ","mesh","D000071960"
> "8791","breast carcinoma in situ","umls","C0154084"
> "8791","breast carcinoma in situ","mondo","0004658"
> "0111528","Naegeli-Franceschetti-Jadassohn syndrome","mesh","C538331"
> "0111528","Naegeli-Franceschetti-Jadassohn syndrome","umls","C0343111"
> "14118","familial lipoprotein lipase deficiency","icd10cm","E78.3"
> "14118","familial lipoprotein lipase deficiency","icd9cm","272.3"
> "14118","familial lipoprotein lipase deficiency","mesh","D008072"
> "14118","familial lipoprotein lipase deficiency","umls","C0023817"
> "14118","familial lipoprotein lipase deficiency","mondo","0009387"
> "3878","intestinal pseudo-obstruction","mesh","D007418"
> "3878","intestinal pseudo-obstruction","umls","C0021847"
> "3878","intestinal pseudo-obstruction","mondo","0002803"
> "3870","childhood central nervous system primitive neuroectodermal neoplasm","umls","C1332957"
> "3870","childhood central nervous system primitive neuroectodermal neoplasm","mondo","0002798"
> "3873","nodular medulloblastoma","umls","C1334970"
> "3873","nodular medulloblastoma","mondo","0002799"
4253,4269c8642,8647
< "9091","REM sleep behavior disorder","icd10cm","G47.52"
< "9091","REM sleep behavior disorder","icd9cm","327.42"
< "9091","REM sleep behavior disorder","mesh","D020187"
< "9091","REM sleep behavior disorder","umls","C0751772"
< "9091","REM sleep behavior disorder","mondo","0005937"
< "2741","bilirubin metabolic disorder","mesh","D006932"
< "2741","bilirubin metabolic disorder","mesh","D006933"
< "2741","bilirubin metabolic disorder","umls","C0020433"
< "2741","bilirubin metabolic disorder","umls","C0020435"
< "2741","bilirubin metabolic disorder","mondo","0002408"
< "11335","sarcoidosis","icd10cm","D80-D89"
< "11335","sarcoidosis","icd10cm","D86"
< "11335","sarcoidosis","icd10cm","D86.9"
< "11335","sarcoidosis","icd9cm","135"
< "11335","sarcoidosis","mesh","D012507"
< "11335","sarcoidosis","umls","C0036202"
< "11335","sarcoidosis","mondo","0019338"
---
> "3876","colonic pseudo-obstruction","mesh","D003112"
> "3876","colonic pseudo-obstruction","umls","C0009377"
> "3876","colonic pseudo-obstruction","mondo","0002801"
> "3877","functional colonic disease","mesh","D003109"
> "3877","functional colonic disease","umls","C0009374"
> "3877","functional colonic disease","mondo","0002802"
4277,4316c8655,8676
< "11337","Lemierre's syndrome","icd9cm","040.3"
< "11337","Lemierre's syndrome","mesh","D005674"
< "11337","Lemierre's syndrome","umls","C0027537"
< "11337","Lemierre's syndrome","mondo","0015306"
< "13270","erythropoietic protoporphyria","icd10cm","E80.0"
< "13270","erythropoietic protoporphyria","mesh","D046351"
< "13270","erythropoietic protoporphyria","umls","C0162568"
< "13270","erythropoietic protoporphyria","mondo","0001676"
< "11339","pneumocystosis","icd10cm","B59"
< "11339","pneumocystosis","icd9cm","136.3"
< "11339","pneumocystosis","mesh","D011020"
< "11339","pneumocystosis","umls","C1535939"
< "11339","pneumocystosis","mondo","0019121"
< "11338","tetanus","icd10cm","A35"
< "11338","tetanus","icd9cm","037"
< "11338","tetanus","mesh","D013742"
< "11338","tetanus","umls","C0039614"
< "11338","tetanus","mondo","0005526"
< "10200","chest wall lipoma","umls","C1332932"
< "10200","chest wall lipoma","mondo","0000971"
< "15","reproductive system disease","umls","C1335037"
< "15","reproductive system disease","mondo","0005039"
< "5719","adrenal medulla cancer","icd10cm","C74.1"
< "5719","adrenal medulla cancer","umls","C0344456"
< "5719","adrenal medulla cancer","umls","C0596046"
< "5719","adrenal medulla cancer","mondo","0003606"
< "5718","adrenal neuroblastoma","umls","C0559460"
< "5718","adrenal neuroblastoma","mondo","0006076"
< "18","urinary system disease","umls","C1335051"
< "18","urinary system disease","mondo","0002118"
< "6408","ovary papillary carcinoma","umls","C1335178"
< "6408","ovary papillary carcinoma","mondo","0003874"
< "8186","fallopian tube gestational choriocarcinoma","umls","C1333593"
< "8186","fallopian tube gestational choriocarcinoma","mondo","0004489"
< "0110805","hereditary spastic paraplegia 53","icd10cm","G11.4"
< "0110805","hereditary spastic paraplegia 53","mondo","0013962"
< "14059","paraurethral gland cancer","icd10cm","C68.1"
< "14059","paraurethral gland cancer","icd9cm","189.4"
< "14059","paraurethral gland cancer","umls","C0153621"
< "14059","paraurethral gland cancer","mondo","0001869"
---
> "8476","Whipple disease","icd10cm","K90.81"
> "8476","Whipple disease","icd9cm","040.2"
> "8476","Whipple disease","mesh","D008061"
> "8476","Whipple disease","umls","C0023788"
> "8476","Whipple disease","mondo","0005116"
> "8472","localized scleroderma","icd10cm","L94.0"
> "8472","localized scleroderma","icd9cm","701.0"
> "8472","localized scleroderma","mesh","D012594"
> "8472","localized scleroderma","umls","C0036420"
> "8472","localized scleroderma","mondo","0019562"
> "7566","eccrine porocarcinoma","mesh","D057090"
> "7566","eccrine porocarcinoma","umls","C1266065"
> "7566","eccrine porocarcinoma","mondo","0006189"
> "7567","vulvar clear cell hidradenocarcinoma","umls","C1520076"
> "7567","vulvar clear cell hidradenocarcinoma","mondo","0004283"
> "7565","vulvar eccrine porocarcinoma","umls","C1520081"
> "7565","vulvar eccrine porocarcinoma","mondo","0004281"
> "0080049","acromesomelic dysplasia","mondo","0019696"
> "10128","venous insufficiency","icd9cm","459.81"
> "10128","venous insufficiency","mesh","D014689"
> "10128","venous insufficiency","umls","C0042485"
> "10128","venous insufficiency","mondo","0000945"
4321,4322d8680
< "0110844","xeroderma pigmentosum group C","icd10cm","Q82.1"
< "0110844","xeroderma pigmentosum group C","mondo","0010211"
4342,4374c8700,8709
< "3904","bronchus carcinoma","mesh","D002283"
< "3904","bronchus carcinoma","umls","C0007121"
< "3904","bronchus carcinoma","mondo","0002806"
< "0050730","coenzyme Q10 deficiency disease","mondo","0018151"
< "3907","lung squamous cell carcinoma","umls","C0149782"
< "3907","lung squamous cell carcinoma","mondo","0005097"
< "0080210","primary mediastinal B-cell lymphoma","icd10cm","C85.2"
< "0080210","primary mediastinal B-cell lymphoma","mondo","0020323"
< "3908","lung non-small cell carcinoma","kegg","05223"
< "3908","lung non-small cell carcinoma","mesh","D002289"
< "3908","lung non-small cell carcinoma","umls","C0007131"
< "3908","lung non-small cell carcinoma","mondo","0005233"
< "6691","Aagenaes syndrome","mesh","C535330"
< "6691","Aagenaes syndrome","umls","C0268314"
< "6691","Aagenaes syndrome","mondo","0008966"
< "0060556","Kufor-Rakeb syndrome","mesh","C537177"
< "0060556","Kufor-Rakeb syndrome","umls","C1847640"
< "0060556","Kufor-Rakeb syndrome","mondo","0011706"
< "0110988","Joubert syndrome 2","mesh","C536294"
< "0110988","Joubert syndrome 2","mondo","0011963"
< "0110989","Joubert syndrome 20","mondo","0013994"
< "4766","embryoma","umls","C0936282"
< "4766","embryoma","mondo","0003127"
< "0110984","Joubert syndrome 15","mondo","0013763"
< "0110985","Joubert syndrome 16","mondo","0013764"
< "0110986","Joubert syndrome 17","mondo","0013824"
< "0110987","Joubert syndrome 18","mondo","0013896"
< "0110980","Joubert syndrome 1","mondo","0008944"
< "3193","peripheral nerve sheath neoplasm","mesh","D018317"
< "3193","peripheral nerve sheath neoplasm","umls","C0751689"
< "3193","peripheral nerve sheath neoplasm","mondo","0002547"
< "0110982","Joubert syndrome 13","mondo","0013608"
< "0110983","Joubert syndrome 14","mondo","0013745"
---
> "10122","hyperpigmentation of eyelid","icd10cm","H02.71"
> "10122","hyperpigmentation of eyelid","icd9cm","374.52"
> "10122","hyperpigmentation of eyelid","mesh","C562400"
> "10122","hyperpigmentation of eyelid","umls","C0155211"
> "10122","hyperpigmentation of eyelid","mondo","0007769"
> "12720","cerebral atherosclerosis","icd10cm","I67.2"
> "12720","cerebral atherosclerosis","icd9cm","437.0"
> "12720","cerebral atherosclerosis","mesh","D002537"
> "12720","cerebral atherosclerosis","umls","C0007775"
> "12720","cerebral atherosclerosis","mondo","0006694"
4381,4430c8716,8730
< "11249","vitamin K deficiency bleeding","icd10cm","E56.1"
< "11249","vitamin K deficiency bleeding","icd9cm","269.0"
< "11249","vitamin K deficiency bleeding","mesh","D014813"
< "11249","vitamin K deficiency bleeding","umls","C0042880"
< "11249","vitamin K deficiency bleeding","mondo","0001244"
< "13891","bird fancier's lung","icd10cm","J67.2"
< "13891","bird fancier's lung","icd9cm","495.2"
< "13891","bird fancier's lung","mesh","D001716"
< "13891","bird fancier's lung","umls","C0005592"
< "13891","bird fancier's lung","mondo","0005668"
< "0090019","sitosterolemia","mesh","C537345"
< "0090019","sitosterolemia","umls","C0342907"
< "0090019","sitosterolemia","mondo","0008863"
< "0040037","aztreonam allergy","umls","C0571476"
< "7263","selective IgD deficiency disease","umls","C0398695"
< "7263","selective IgD deficiency disease","mondo","0004165"
< "9958","hemometra","icd10cm","N85.7"
< "9958","hemometra","icd9cm","621.4"
< "9958","hemometra","mesh","D006409"
< "9958","hemometra","umls","C0018948"
< "9958","hemometra","mondo","0006782"
< "0110593","autosomal dominant nonsyndromic deafness 9","icd10cm","H90.3"
< "0110593","autosomal dominant nonsyndromic deafness 9","mondo","0011058"
< "9952","acute lymphocytic leukemia","icd10cm","C91.0"
< "9952","acute lymphocytic leukemia","icd10cm","C91.00"
< "9952","acute lymphocytic leukemia","icd9cm","204.0"
< "9952","acute lymphocytic leukemia","umls","C0023449"
< "9952","acute lymphocytic leukemia","mondo","0004967"
< "0060870","isolated growth hormone deficiency","icd10cm","E23.0"
< "0060870","isolated growth hormone deficiency","icd9cm","253.3"
< "0060870","isolated growth hormone deficiency","mesh","D004393"
< "0060870","isolated growth hormone deficiency","umls","C0013338"
< "0060870","isolated growth hormone deficiency","mondo","0000050"
< "0110535","autosomal recessive nonsyndromic deafness 9","icd10cm","H90.3"
< "0110535","autosomal recessive nonsyndromic deafness 9","mondo","0010986"
< "203","exostosis","icd10cm","M27.8"
< "203","exostosis","icd9cm","726.91"
< "203","exostosis","mesh","D005096"
< "203","exostosis","umls","C1442903"
< "203","exostosis","mondo","0002181"
< "0060873","isolated growth hormone deficiency type IA","icd10cm","E23.0"
< "0060873","isolated growth hormone deficiency type IA","mondo","0009876"
< "0060874","isolated growth hormone deficiency type IB","icd10cm","E23.0"
< "0060874","isolated growth hormone deficiency type IB","mondo","0013006"
< "0060875","isolated growth hormone deficiency type III","icd10cm","E23.0"
< "0060875","isolated growth hormone deficiency type III","mondo","0010615"
< "206","hereditary multiple exostoses","icd10cm","Q78.6"
< "206","hereditary multiple exostoses","mesh","D005097"
< "206","hereditary multiple exostoses","umls","C0015306"
< "206","hereditary multiple exostoses","mondo","0005508"
---
> "4163","ganglioneuroblastoma","mesh","D018305"
> "4163","ganglioneuroblastoma","umls","C0206718"
> "4163","ganglioneuroblastoma","mondo","0005035"
> "4160","differentiating neuroblastoma","umls","C1511934"
> "4160","differentiating neuroblastoma","mondo","0002899"
> "10435","purulent acute otitis media","icd9cm","382.02"
> "10435","purulent acute otitis media","umls","C0155439"
> "10435","purulent acute otitis media","mondo","0001031"
> "0080106","microcephaly and chorioretinopathy 2","mondo","0014516"
> "0080107","microcephaly and chorioretinopathy 3","mondo","0014592"
> "0050719","cerebral folate receptor alpha deficiency","mondo","0013110"
> "0080102","congenital fiber-type disproportion","mondo","0000865"
> "0080103","cylindrical spirals myopathy","mondo","0008058"
> "0080100","congenital myopathy","mondo","0019952"
> "0080101","Compton-North congenital myopathy","mondo","0012929"
4433,4436c8733,8734
< "2615","papilloma","mesh","D010212"
< "2615","papilloma","umls","C0030354"
< "2615","papilloma","umls","C0205875"
< "2615","papilloma","mondo","0002363"
---
> "0050246","granulomatous amebic encephalitis","mondo","0000291"
> "0050711","aceruloplasminemia","mondo","0011426"
4441,4446c8739,8743
< "12680","pseudobulbar palsy","icd9cm","335.23"
< "12680","pseudobulbar palsy","mesh","D020828"
< "12680","pseudobulbar palsy","umls","C0033790"
< "12680","pseudobulbar palsy","mondo","0006930"
< "0110608","primary ciliary dyskinesia 19","icd10cm","Q34.8"
< "0110608","primary ciliary dyskinesia 19","mondo","0013979"
---
> "13143","benign secondary hypertension","icd9cm","405.1"
> "13143","benign secondary hypertension","umls","C0155620"
> "13143","benign secondary hypertension","mondo","0001646"
> "2239","granulomatous hepatitis","umls","C0235369"
> "2239","granulomatous hepatitis","mondo","0002252"
4448,4461c8745
< "12683","vestibular neuronitis","icd10cm","A88.1"
< "12683","vestibular neuronitis","icd10cm","H81.2"
< "12683","vestibular neuronitis","icd10cm","H81.20"
< "12683","vestibular neuronitis","icd9cm","078.81"
< "12683","vestibular neuronitis","icd9cm","386.12"
< "12683","vestibular neuronitis","mesh","D020338"
< "12683","vestibular neuronitis","umls","C0751908"
< "12683","vestibular neuronitis","mondo","0006008"
< "0110801","hereditary spastic paraplegia 49","icd10cm","G11.4"
< "0110801","hereditary spastic paraplegia 49","mondo","0014016"
< "13146","esophageal candidiasis","icd10cm","B37.81"
< "13146","esophageal candidiasis","icd9cm","112.84"
< "13146","esophageal candidiasis","umls","C0239295"
< "13146","esophageal candidiasis","mondo","0001648"
---
> "0111009","cone-rod dystrophy 1","mondo","0010905"
4476,4480c8760,8764
< "0111005","cone-rod dystrophy 2","mondo","0007362"
< "13148","acute cystitis","icd10cm","N30.0"
< "13148","acute cystitis","icd9cm","595.0"
< "13148","acute cystitis","umls","C0149523"
< "13148","acute cystitis","mondo","0001650"
---
> "2236","congenital afibrinogenemia","mesh","D000347"
> "2236","congenital afibrinogenemia","umls","C0001733"
> "2236","congenital afibrinogenemia","mondo","0008737"
> "5936","ovarian mixed germ cell neoplasm","umls","C0280135"
> "5936","ovarian mixed germ cell neoplasm","mondo","0003710"
4483,4499c8767,8775
< "10825","essential hypertension","icd10cm","I10"
< "10825","essential hypertension","icd9cm","401"
< "10825","essential hypertension","icd9cm","401.9"
< "10825","essential hypertension","mesh","D000075222"
< "10825","essential hypertension","umls","C0085580"
< "10825","essential hypertension","mondo","0001134"
< "0090128","dilated cardiomyopathy with woolly hair and keratoderma","mondo","0011581"
< "0070000","3-methylglutaconic aciduria type VIII","mondo","0014988"
< "0110800","hereditary spastic paraplegia 48","icd10cm","G11.4"
< "0110800","hereditary spastic paraplegia 48","mondo","0013342"
< "7843","female breast carcinoma","umls","C0007104"
< "7843","female breast carcinoma","mondo","0004379"
< "0070005","Seckel syndrome 9","mondo","0014767"
< "0070006","Seckel syndrome 6","mondo","0013871"
< "0070007","Seckel syndrome 1","mondo","0008869"
< "0070008","Seckel syndrome 10","mondo","0014991"
< "0070009","Seckel syndrome 8","mondo","0014350"
---
> "0080361","trimethylaminuria","mesh","C536561"
> "3498","pancreatic ductal adenocarcinoma","umls","C1335302"
> "3498","pancreatic ductal adenocarcinoma","mondo","0005184"
> "3499","gallbladder signet ring cell adenocarcinoma","umls","C1333758"
> "3499","gallbladder signet ring cell adenocarcinoma","mondo","0002667"
> "3497","pancreatic signet ring cell adenocarcinoma","umls","C1335317"
> "3497","pancreatic signet ring cell adenocarcinoma","mondo","0002666"
> "3494","bile duct signet ring cell carcinoma","umls","C0861859"
> "3494","bile duct signet ring cell carcinoma","mondo","0002664"
4513,4515c8789,8800
< "0070225","progressive familial intrahepatic cholestasis 5","mondo","0014884"
< "2097","vulval Paget's disease","umls","C1275217"
< "2097","vulval Paget's disease","mondo","0002207"
---
> "3491","Turner syndrome","icd10cm","Q96"
> "3491","Turner syndrome","icd10cm","Q96.0"
> "3491","Turner syndrome","icd10cm","Q96.9"
> "3491","Turner syndrome","mesh","D014424"
> "3491","Turner syndrome","umls","C0041408"
> "3491","Turner syndrome","umls","C1527168"
> "3491","Turner syndrome","mondo","0019499"
> "2095","sweat gland cancer","icd10cm","C44"
> "2095","sweat gland cancer","umls","C1321904"
> "2095","sweat gland cancer","mondo","0002206"
> "13403","neurosarcoidosis","umls","C0398676"
> "13403","neurosarcoidosis","mondo","0001706"
4524,4525c8809,8810
< "2093","vulvar melanoma","umls","C0241989"
< "2093","vulvar melanoma","mondo","0002205"
---
> "13407","hypercalcemic sarcoidosis","umls","C1334067"
> "13407","hypercalcemic sarcoidosis","mondo","0001709"
4529a8815,8818
> "13409","perforation of bile duct","icd10cm","K83.2"
> "13409","perforation of bile duct","icd9cm","576.3"
> "13409","perforation of bile duct","umls","C0156218"
> "13409","perforation of bile duct","mondo","0001710"
4532,4535d8820
< "3652","Leigh disease","icd10cm","G31.82"
< "3652","Leigh disease","mesh","D007888"
< "3652","Leigh disease","umls","C0023264"
< "3652","Leigh disease","mondo","0018859"
4576,4577c8861,8864
< "5983","kidney osteogenic sarcoma","umls","C1335747"
< "5983","kidney osteogenic sarcoma","mondo","0003721"
---
> "223","basilar artery insufficiency","icd9cm","435.0"
> "223","basilar artery insufficiency","mesh","D014715"
> "223","basilar artery insufficiency","umls","C0004812"
> "223","basilar artery insufficiency","mondo","0002250"
4583,4697c8870,8877
< "12029","sympathetic ophthalmia","icd10cm","H44.13"
< "12029","sympathetic ophthalmia","icd9cm","360.11"
< "12029","sympathetic ophthalmia","mesh","D009879"
< "12029","sympathetic ophthalmia","umls","C0029077"
< "12029","sympathetic ophthalmia","mondo","0019198"
< "0060255","rippling muscle disease 2","icd10cm","G71.0"
< "0060255","rippling muscle disease 2","mesh","C535686"
< "0060255","rippling muscle disease 2","umls","C1853698"
< "0060255","rippling muscle disease 2","mondo","0019947"
< "0060812","syndromic X-linked intellectual disability Siderius type","mesh","C537333"
< "0060812","syndromic X-linked intellectual disability Siderius type","umls","C1846055"
< "0060812","syndromic X-linked intellectual disability Siderius type","mondo","0010286"
< "0110108","atrial heart septal defect 3","icd10cm","Q21.1"
< "0110108","atrial heart septal defect 3","mondo","0013567"
< "4492","avian influenza","icd10cm","J09.X"
< "4492","avian influenza","mesh","D005585"
< "4492","avian influenza","umls","C0016627"
< "4492","avian influenza","mondo","0018695"
< "10354","breast fibrocystic disease","icd10cm","N60"
< "10354","breast fibrocystic disease","icd10cm","N60.1"
< "10354","breast fibrocystic disease","icd9cm","610.1"
< "10354","breast fibrocystic disease","mesh","D005348"
< "10354","breast fibrocystic disease","umls","C0016034"
< "10354","breast fibrocystic disease","mondo","0005219"
< "4889","lymph node tuberculosis","icd10cm","A18.2"
< "4889","lymph node tuberculosis","mesh","D014388"
< "4889","lymph node tuberculosis","mesh","D018601"
< "4889","lymph node tuberculosis","umls","C0041316"
< "4889","lymph node tuberculosis","umls","C0242830"
< "4889","lymph node tuberculosis","mondo","0005831"
< "0050661","vitelliform macular dystrophy","icd10cm","H35.5"
< "0050661","vitelliform macular dystrophy","mesh","D057826"
< "0050661","vitelliform macular dystrophy","mondo","0000390"
< "10350","breast cyst","icd10cm","N60.0"
< "10350","breast cyst","mesh","D047688"
< "10350","breast cyst","umls","C0006144"
< "10350","breast cyst","mondo","0001011"
< "9786","bulbar polio","icd9cm","045.0"
< "9786","bulbar polio","mesh","D011052"
< "9786","bulbar polio","umls","C0032372"
< "9786","bulbar polio","mondo","0005684"
< "10352","breast fibroadenosis","icd10cm","N60.2"
< "10352","breast fibroadenosis","icd9cm","610.2"
< "10352","breast fibroadenosis","umls","C1305875"
< "10352","breast fibroadenosis","mondo","0001012"
< "10353","fibrosclerosis of breast","icd10cm","N60.3"
< "10353","fibrosclerosis of breast","icd9cm","610.3"
< "10353","fibrosclerosis of breast","umls","C0156318"
< "10353","fibrosclerosis of breast","mondo","0006118"
< "4880","kidney clear cell sarcoma","umls","C0334488"
< "4880","kidney clear cell sarcoma","mondo","0005006"
< "9370","exophthalmos","icd10cm","H05.20"
< "9370","exophthalmos","icd9cm","376.30"
< "9370","exophthalmos","mesh","D005094"
< "9370","exophthalmos","umls","C0015300"
< "9370","exophthalmos","mondo","0004770"
< "13381","pernicious anemia","icd10cm","D51.0"
< "13381","pernicious anemia","icd9cm","281.0"
< "13381","pernicious anemia","mesh","D000752"
< "13381","pernicious anemia","umls","C0002892"
< "13381","pernicious anemia","mondo","0008228"
< "9375","Fuchs' heterochromic uveitis","icd10cm","H20.81"
< "9375","Fuchs' heterochromic uveitis","icd9cm","364.21"
< "9375","Fuchs' heterochromic uveitis","umls","C0016782"
< "9375","Fuchs' heterochromic uveitis","mondo","0004771"
< "4885","Colorado tick fever","icd10cm","A93.2"
< "4885","Colorado tick fever","mesh","D003121"
< "4885","Colorado tick fever","umls","C0009400"
< "4885","Colorado tick fever","mondo","0005708"
< "10688","hypertrophy of breast","icd10cm","N62"
< "10688","hypertrophy of breast","icd9cm","611.1"
< "10688","hypertrophy of breast","umls","C0020565"
< "10688","hypertrophy of breast","mondo","0001100"
< "0070138","autosomal recessive cutis laxa type IIIB","icd10cm","Q82.8"
< "0070138","autosomal recessive cutis laxa type IIIB","mondo","0013755"
< "0070139","autosomal recessive cutis laxa type IC","mesh","C567716"
< "0070139","autosomal recessive cutis laxa type IC","umls","C2750804"
< "0070139","autosomal recessive cutis laxa type IC","mondo","0013170"
< "0070134","autosomal recessive cutis laxa type IIA","icd10cm","Q82.8"
< "0070134","autosomal recessive cutis laxa type IIA","mondo","0018163"
< "0111024","cone-rod dystrophy 18","mondo","0014153"
< "0070136","autosomal dominant cutis laxa 2","icd10cm","Q82.8"
< "0070136","autosomal dominant cutis laxa 2","mondo","0009054"
< "9174","rectum carcinoma in situ","icd10cm","D01.2"
< "9174","rectum carcinoma in situ","icd9cm","230.4"
< "9174","rectum carcinoma in situ","umls","C0154062"
< "9174","rectum carcinoma in situ","mondo","0004725"
< "0070130","autosomal dominant cutis laxa 1","icd10cm","Q82.8"
< "0070130","autosomal dominant cutis laxa 1","mondo","0007411"
< "0070131","autosomal dominant cutis laxa 3","icd10cm","Q82.8"
< "0070131","autosomal dominant cutis laxa 3","mondo","0014706"
< "0070132","autosomal recessive cutis laxa type IIIA","icd10cm","Q82.8"
< "0070132","autosomal recessive cutis laxa type IIIA","mondo","0009053"
< "0070133","autosomal recessive cutis laxa type IB","icd10cm","Q82.8"
< "0070133","autosomal recessive cutis laxa type IB","mondo","0013754"
< "13222","submucous uterine fibroid","icd10cm","D25.0"
< "13222","submucous uterine fibroid","icd9cm","218.0"
< "13222","submucous uterine fibroid","umls","C0153993"
< "13222","submucous uterine fibroid","mondo","0001664"
< "2215","factor VII deficiency","icd10cm","D68.2"
< "2215","factor VII deficiency","mesh","D005168"
< "2215","factor VII deficiency","umls","C0015503"
< "2215","factor VII deficiency","mondo","0009211"
< "1825","childhood absence epilepsy","mesh","D004832"
< "1825","childhood absence epilepsy","umls","C0014553"
< "1825","childhood absence epilepsy","mondo","0010826"
< "1827","idiopathic generalized epilepsy","mesh","D004829"
< "1827","idiopathic generalized epilepsy","umls","C0014548"
< "1827","idiopathic generalized epilepsy","mondo","0005579"
< "1826","epilepsy","icd10cm","G40.9"
< "1826","epilepsy","icd10cm","G40.909"
< "1826","epilepsy","icd9cm","345.9"
< "1826","epilepsy","mesh","D004827"
< "1826","epilepsy","umls","C0014544"
< "1826","epilepsy","mondo","0005027"
---
> "11669","hypertrichosis of eyelid","icd10cm","H02.86"
> "11669","hypertrichosis of eyelid","icd9cm","374.54"
> "11669","hypertrichosis of eyelid","umls","C0155213"
> "11669","hypertrichosis of eyelid","mondo","0001334"
> "11668","hypopigmentation of eyelid","icd10cm","H02.73"
> "11668","hypopigmentation of eyelid","icd9cm","374.53"
> "11668","hypopigmentation of eyelid","umls","C0155212"
> "11668","hypopigmentation of eyelid","mondo","0006561"
4702,4710c8882,8883
< "9577","neonatal candidiasis","icd10cm","P37.5"
< "9577","neonatal candidiasis","icd9cm","771.7"
< "9577","neonatal candidiasis","umls","C0276682"
< "9577","neonatal candidiasis","mondo","0004824"
< "2142","urethra leiomyoma","umls","C1336888"
< "2142","urethra leiomyoma","mondo","0002222"
< "4974","actinobacillosis","mesh","D000187"
< "4974","actinobacillosis","umls","C0001247"
< "4974","actinobacillosis","mondo","0005630"
---
> "0110751","type 1 diabetes mellitus 12","icd10cm","E10"
> "0110751","type 1 diabetes mellitus 12","mondo","0011068"
4719,4729c8892,8895
< "4971","myelofibrosis","icd10cm","D47.4"
< "4971","myelofibrosis","icd10cm","D75.81"
< "4971","myelofibrosis","icd9cm","238.76"
< "4971","myelofibrosis","icd9cm","289.83"
< "4971","myelofibrosis","mesh","D055728"
< "4971","myelofibrosis","umls","C0001815"
< "4971","myelofibrosis","umls","C0026987"
< "4971","myelofibrosis","mondo","0009692"
< "4972","myelodysplastic/myeloproliferative neoplasm","mesh","D054437"
< "4972","myelodysplastic/myeloproliferative neoplasm","umls","C1301355"
< "4972","myelodysplastic/myeloproliferative neoplasm","mondo","0006311"
---
> "0110754","type 1 diabetes mellitus 17","icd10cm","E10"
> "0110754","type 1 diabetes mellitus 17","mondo","0011302"
> "0110757","type 1 diabetes mellitus 20","icd10cm","E10"
> "0110757","type 1 diabetes mellitus 20","mondo","0012919"
4732,4786c8898,8902
< "0060367","autosomal dominant Parkinson's disease 1","mondo","0008200"
< "5390","clear cell adenoma","umls","C0334315"
< "5390","clear cell adenoma","mondo","0003426"
< "10534","stomach cancer","icd10cm","C16"
< "10534","stomach cancer","icd10cm","C16.2"
< "10534","stomach cancer","icd10cm","C16.5"
< "10534","stomach cancer","icd10cm","C16.6"
< "10534","stomach cancer","icd10cm","C16.9"
< "10534","stomach cancer","icd9cm","151"
< "10534","stomach cancer","icd9cm","151.4"
< "10534","stomach cancer","icd9cm","151.5"
< "10534","stomach cancer","icd9cm","151.6"
< "10534","stomach cancer","icd9cm","151.9"
< "10534","stomach cancer","mesh","D013274"
< "10534","stomach cancer","umls","C0024623"
< "10534","stomach cancer","umls","C0038356"
< "10534","stomach cancer","umls","C0153421"
< "10534","stomach cancer","umls","C0153422"
< "10534","stomach cancer","umls","C0153423"
< "10534","stomach cancer","mondo","0001056"
< "5396","prolactin producing pituitary tumor","umls","C0278863"
< "5396","prolactin producing pituitary tumor","umls","C1334614"
< "5396","prolactin producing pituitary tumor","mondo","0003430"
< "10538","gastric fundus cancer","icd10cm","C16.1"
< "10538","gastric fundus cancer","icd9cm","151.3"
< "10538","gastric fundus cancer","umls","C0153420"
< "10538","gastric fundus cancer","mondo","0001058"
< "1920","hyperuricemia","mesh","D033461"
< "1920","hyperuricemia","umls","C0740394"
< "1920","hyperuricemia","mondo","0002144"
< "3277","thymus cancer","icd10cm","C37"
< "3277","thymus cancer","icd9cm","164.0"
< "3277","thymus cancer","mesh","D013953"
< "3277","thymus cancer","umls","C0751552"
< "3277","thymus cancer","mondo","0002586"
< "3274","proliferative type fibrocystic change of breast","umls","C0334056"
< "3274","proliferative type fibrocystic change of breast","mondo","0002585"
< "1925","Coffin-Siris syndrome","mesh","C536436"
< "1925","Coffin-Siris syndrome","umls","C0265338"
< "1925","Coffin-Siris syndrome","mondo","0015452"
< "1926","Gaucher's disease","icd10cm","E75.22"
< "1926","Gaucher's disease","mesh","D005776"
< "1926","Gaucher's disease","umls","C0017205"
< "1926","Gaucher's disease","mondo","0018150"
< "1927","sphingolipidosis","icd10cm","E75.3"
< "1927","sphingolipidosis","mesh","D013106"
< "1927","sphingolipidosis","umls","C0037899"
< "1927","sphingolipidosis","mondo","0019255"
< "1929","supravalvular aortic stenosis","icd10cm","Q25.3"
< "1929","supravalvular aortic stenosis","mesh","D021921"
< "1929","supravalvular aortic stenosis","umls","C0003499"
< "1929","supravalvular aortic stenosis","mondo","0008504"
< "4226","endometrial stromal sarcoma","mesh","D018203"
< "4226","endometrial stromal sarcoma","umls","C0206630"
< "4226","endometrial stromal sarcoma","mondo","0006745"
---
> "13768","opisthorchiasis","icd10cm","B66.0"
> "13768","opisthorchiasis","icd9cm","121.0"
> "13768","opisthorchiasis","mesh","D009889"
> "13768","opisthorchiasis","umls","C0029106"
> "13768","opisthorchiasis","mondo","0005884"
4788,4789c8904
< "0110534","autosomal recessive nonsyndromic deafness 89","icd10cm","H90.3"
< "0110534","autosomal recessive nonsyndromic deafness 89","mondo","0013489"
---
> "0070229","intrahepatic cholestasis of pregnancy 3","mondo","0013995"
4802c8917,8918
< "0070220","familial hyperinsulinemic hypoglycemia 5","mondo","0012381"
---
> "7360","solid pattern testicular yolk sac tumor","umls","C1515312"
> "7360","solid pattern testicular yolk sac tumor","mondo","0004198"
4809,4811c8925
< "0070223","progressive familial intrahepatic cholestasis 3","mesh","C535935"
< "0070223","progressive familial intrahepatic cholestasis 3","umls","C1865643"
< "0070223","progressive familial intrahepatic cholestasis 3","mondo","0011214"
---
> "7363","vulvar keratinizing squamous cell carcinoma","mondo","0004199"
4813,4814c8927,8929
< "0110538","autosomal recessive nonsyndromic deafness 96","icd10cm","H90.3"
< "0110538","autosomal recessive nonsyndromic deafness 96","mondo","0013738"
---
> "7365","Kimura disease","mesh","D000796"
> "7365","Kimura disease","umls","C0033838"
> "7365","Kimura disease","mondo","0018830"
4819,4827c8934,8937
< "3691","anal colloid adenocarcinoma","umls","C1332272"
< "3691","anal colloid adenocarcinoma","mondo","0002734"
< "13223","uterine fibroid","icd10cm","D25"
< "13223","uterine fibroid","icd10cm","D25.9"
< "13223","uterine fibroid","icd9cm","218"
< "13223","uterine fibroid","icd9cm","218.9"
< "13223","uterine fibroid","mesh","D007889"
< "13223","uterine fibroid","umls","C0042133"
< "13223","uterine fibroid","mondo","0007886"
---
> "12311","stromal corneal pigmentation","icd10cm","H18.06"
> "12311","stromal corneal pigmentation","icd9cm","371.12"
> "12311","stromal corneal pigmentation","umls","C0155105"
> "12311","stromal corneal pigmentation","mondo","0006613"
4831,4834c8941,8950
< "13226","oculoglandular tularemia","icd10cm","A21.1"
< "13226","oculoglandular tularemia","icd9cm","021.3"
< "13226","oculoglandular tularemia","umls","C0152944"
< "13226","oculoglandular tularemia","mondo","0001665"
---
> "12318","granular corneal dystrophy","icd10cm","H18.53"
> "12318","granular corneal dystrophy","icd9cm","371.53"
> "12318","granular corneal dystrophy","mesh","D003317"
> "12318","granular corneal dystrophy","umls","C0018179"
> "12318","granular corneal dystrophy","mondo","0001490"
> "12918","thromboangiitis obliterans","icd10cm","I73.1"
> "12918","thromboangiitis obliterans","icd9cm","443.1"
> "12918","thromboangiitis obliterans","mesh","D013919"
> "12918","thromboangiitis obliterans","umls","C0040021"
> "12918","thromboangiitis obliterans","mondo","0008889"
4839,4857d8954
< "0110249","cataract 11 multiple types","icd10cm","Q12.0"
< "0110249","cataract 11 multiple types","mondo","0012527"
< "0110248","cataract 30","icd10cm","Q12.0"
< "0110248","cataract 30","mondo","0007286"
< "0110711","congenital hypotrichosis with juvenile macular dystrophy","mondo","0011107"
< "0110243","cataract 46 juvenile-onset","icd10cm","Q12.0"
< "0110243","cataract 46 juvenile-onset","mondo","0008925"
< "0110242","cataract 13 with adult i phenotype","icd10cm","Q12.0"
< "0110242","cataract 13 with adult i phenotype","mondo","0007289"
< "0110241","cataract 41","icd10cm","Q12.0"
< "0110241","cataract 41","mondo","0007287"
< "0110240","cataract 20 multiple types","icd10cm","Q12.0"
< "0110240","cataract 20 multiple types","mondo","0007284"
< "0110247","cataract 36","mondo","0013484"
< "0110246","cataract 26 multiple types","icd10cm","Q12.0"
< "0110246","cataract 26 multiple types","mondo","0011591"
< "0110245","cataract 38","icd10cm","Q12.0"
< "0110245","cataract 38","mondo","0013859"
< "0110244","cataract 28","mondo","0012175"
4862,4924c8959,8971
< "2352","hemochromatosis","icd10cm","E83.11"
< "2352","hemochromatosis","icd10cm","E83.110"
< "2352","hemochromatosis","icd10cm","E83.119"
< "2352","hemochromatosis","mesh","D006432"
< "2352","hemochromatosis","umls","C0018995"
< "2352","hemochromatosis","mondo","0006507"
< "14239","gastrointestinal tularemia","icd9cm","021.1"
< "14239","gastrointestinal tularemia","icd9cm","021.8"
< "14239","gastrointestinal tularemia","umls","C0029835"
< "14239","gastrointestinal tularemia","umls","C0152942"
< "14239","gastrointestinal tularemia","mondo","0001916"
< "5488","mediastinum synovial sarcoma","umls","C1334681"
< "5488","mediastinum synovial sarcoma","mondo","0003467"
< "3310","atopic dermatitis","icd10cm","L20"
< "3310","atopic dermatitis","icd10cm","L20.81"
< "3310","atopic dermatitis","icd10cm","L20.9"
< "3310","atopic dermatitis","mesh","D003876"
< "3310","atopic dermatitis","umls","C0011615"
< "3310","atopic dermatitis","mondo","0004980"
< "3312","bipolar disorder","icd10cm","F31"
< "3312","bipolar disorder","icd10cm","F31.9"
< "3312","bipolar disorder","icd9cm","296.40"
< "3312","bipolar disorder","icd9cm","296.60"
< "3312","bipolar disorder","icd9cm","296.80"
< "3312","bipolar disorder","mesh","D001714"
< "3312","bipolar disorder","umls","C0005586"
< "3312","bipolar disorder","umls","C0005587"
< "3312","bipolar disorder","umls","C0024713"
< "3312","bipolar disorder","umls","C0236780"
< "3312","bipolar disorder","mondo","0004985"
< "3315","lipoma","icd10cm","D17"
< "3315","lipoma","icd10cm","D17.9"
< "3315","lipoma","icd9cm","214"
< "3315","lipoma","icd9cm","214.9"
< "3315","lipoma","mesh","D008067"
< "3315","lipoma","mesh","D018205"
< "3315","lipoma","umls","C0023798"
< "3315","lipoma","umls","C0206631"
< "3315","lipoma","umls","C0346118"
< "3315","lipoma","mondo","0005106"
< "3314","angiomyolipoma","mesh","D018207"
< "3314","angiomyolipoma","umls","C0206633"
< "3314","angiomyolipoma","mondo","0002603"
< "10223","dermatomyositis","icd10cm","M33"
< "10223","dermatomyositis","icd10cm","M33.9"
< "10223","dermatomyositis","icd10cm","M33.90"
< "10223","dermatomyositis","icd9cm","710.3"
< "10223","dermatomyositis","mesh","D003882"
< "10223","dermatomyositis","umls","C0011633"
< "10223","dermatomyositis","mondo","0016367"
< "9395","croup","icd10cm","J05.0"
< "9395","croup","icd9cm","464.4"
< "9395","croup","mesh","D003440"
< "9395","croup","umls","C0010380"
< "9395","croup","mondo","0005722"
< "0060205","amyotrophic lateral sclerosis type 14","mondo","0013501"
< "9392","tracheitis","icd10cm","J04.1"
< "9392","tracheitis","icd9cm","464.1"
< "9392","tracheitis","mesh","D014136"
< "9392","tracheitis","umls","C0040584"
< "9392","tracheitis","umls","C0149513"
< "9392","tracheitis","mondo","0005990"
< "0040046","nickel allergic contact dermatitis","icd10cm","L23.0"
---
> "7024","mucinous intrahepatic cholangiocarcinoma","umls","C1513718"
> "7024","mucinous intrahepatic cholangiocarcinoma","mondo","0004078"
> "9008","psoriatic arthritis","icd10cm","L40.5"
> "9008","psoriatic arthritis","icd10cm","L40.50"
> "9008","psoriatic arthritis","icd9cm","696.0"
> "9008","psoriatic arthritis","mesh","D015535"
> "9008","psoriatic arthritis","umls","C0003872"
> "9008","psoriatic arthritis","mondo","0011849"
> "0110599","primary ciliary dyskinesia 3","icd10cm","Q34.8"
> "0110599","primary ciliary dyskinesia 3","mondo","0012085"
> "3331","frontal lobe epilepsy","mesh","D017034"
> "3331","frontal lobe epilepsy","umls","C0085541"
> "3331","frontal lobe epilepsy","mondo","0002612"
4927,4968c8974,8975
< "9398","epiglottitis","icd10cm","J05.1"
< "9398","epiglottitis","icd10cm","J05.10"
< "9398","epiglottitis","icd9cm","464.3"
< "9398","epiglottitis","mesh","D004826"
< "9398","epiglottitis","umls","C0014541"
< "9398","epiglottitis","umls","C0155814"
< "9398","epiglottitis","mondo","0005753"
< "0110401","retinitis pigmentosa 74","icd10cm","H35.5"
< "0110401","retinitis pigmentosa 74","mondo","0014692"
< "13134","hordeolum externum","icd10cm","H00.01"
< "13134","hordeolum externum","icd10cm","H00.03"
< "13134","hordeolum externum","icd9cm","373.11"
< "13134","hordeolum externum","umls","C0019919"
< "13134","hordeolum externum","mondo","0001642"
< "0110403","retinitis pigmentosa 13","icd10cm","H35.5"
< "0110403","retinitis pigmentosa 13","mondo","0010806"
< "0110402","retinitis pigmentosa 45","icd10cm","H35.5"
< "0110402","retinitis pigmentosa 45","mondo","0013413"
< "0110405","retinitis pigmentosa 36","icd10cm","H35.5"
< "0110405","retinitis pigmentosa 36","mondo","0012523"
< "0110404","retinitis pigmentosa 17","icd10cm","H35.5"
< "0110404","retinitis pigmentosa 17","mondo","0010945"
< "0110407","retinitis pigmentosa 57","icd10cm","H35.5"
< "0110407","retinitis pigmentosa 57","mondo","0013315"
< "0110406","retinitis pigmentosa 30","icd10cm","H35.5"
< "0110406","retinitis pigmentosa 30","mondo","0011935"
< "0110409","retinitis pigmentosa 46","icd10cm","H35.5"
< "0110409","retinitis pigmentosa 46","mondo","0012943"
< "0110408","retinitis pigmentosa 11","icd10cm","H35.5"
< "0110408","retinitis pigmentosa 11","mondo","0010828"
< "4159","skin cancer","mesh","D012878"
< "4159","skin cancer","umls","C0007114"
< "4159","skin cancer","mondo","0002898"
< "0110598","primary ciliary dyskinesia 14","icd10cm","Q34.8"
< "0110598","primary ciliary dyskinesia 14","mondo","0013434"
< "6579","chest wall bone cancer","umls","C1334572"
< "6579","chest wall bone cancer","mondo","0003933"
< "8997","polycythemia vera","icd10cm","D45"
< "8997","polycythemia vera","icd9cm","238.4"
< "8997","polycythemia vera","mesh","D011087"
< "8997","polycythemia vera","umls","C0032463"
< "8997","polycythemia vera","mondo","0009891"
---
> "0110831","Usher syndrome type 1D","icd10cm","H35.5"
> "0110831","Usher syndrome type 1D","mondo","0010984"
4970a8978,8982
> "0060192","Crohn's colitis","icd10cm","K50.1"
> "0060192","Crohn's colitis","icd9cm","555.1"
> "0060192","Crohn's colitis","mesh","D003424"
> "0060192","Crohn's colitis","umls","C0156147"
> "0060192","Crohn's colitis","mondo","0005532"
4973,4976c8985,8992
< "3001","female reproductive endometrioid cancer","umls","C0474809"
< "3001","female reproductive endometrioid cancer","mondo","0002480"
< "0060196","amyotrophic lateral sclerosis type 4","icd10cm","G12.2"
< "0060196","amyotrophic lateral sclerosis type 4","mondo","0011223"
---
> "0060190","ileocolitis","icd10cm","K52.9"
> "0060190","ileocolitis","mondo","0005534"
> "0060197","amyotrophic lateral sclerosis type 5","mondo","0011196"
> "9834","hyperopia","icd10cm","H52.0"
> "9834","hyperopia","icd9cm","367.0"
> "9834","hyperopia","mesh","D006956"
> "9834","hyperopia","umls","C0020490"
> "9834","hyperopia","mondo","0004891"
4980d8995
< "0050547","familial medullary thyroid carcinoma","mondo","0007958"
4983,4998d8997
< "3009","breast neuroendocrine neoplasm","umls","C1332635"
< "3009","breast neuroendocrine neoplasm","mondo","0002485"
< "3008","invasive ductal carcinoma","mesh","D018270"
< "3008","invasive ductal carcinoma","umls","C1134719"
< "3008","invasive ductal carcinoma","umls","C1527349"
< "3008","invasive ductal carcinoma","mondo","0004953"
< "154","mixed cell type cancer","mesh","D018198"
< "154","mixed cell type cancer","umls","C0206625"
< "154","mixed cell type cancer","umls","C1368354"
< "154","mixed cell type cancer","mondo","0005853"
< "0060203","amyotrophic lateral sclerosis type 12","mondo","0013264"
< "0060202","amyotrophic lateral sclerosis type 11","mondo","0012945"
< "0060201","amyotrophic lateral sclerosis type 10","mondo","0012790"
< "0060200","amyotrophic lateral sclerosis type 9","mondo","0012753"
< "0060207","amyotrophic lateral sclerosis type 16","mondo","0013715"
< "0060206","amyotrophic lateral sclerosis type 15","mondo","0010459"
5001,5038c9000,9010
< "0060209","amyotrophic lateral sclerosis type 18","mondo","0013891"
< "0060208","amyotrophic lateral sclerosis type 17","mondo","0013861"
< "1586","rheumatic fever","icd10cm","I00"
< "1586","rheumatic fever","icd10cm","I00-I02"
< "1586","rheumatic fever","icd9cm","390"
< "1586","rheumatic fever","icd9cm","390-392.99"
< "1586","rheumatic fever","mesh","D012213"
< "1586","rheumatic fever","umls","C0035436"
< "1586","rheumatic fever","umls","C0264743"
< "1586","rheumatic fever","mondo","0017767"
< "7152","prostate stromal sarcoma","umls","C1335521"
< "7152","prostate stromal sarcoma","mondo","0004124"
< "1584","acute chest syndrome","icd9cm","517.3"
< "1584","acute chest syndrome","mesh","D056586"
< "1584","acute chest syndrome","umls","C0742343"
< "1584","acute chest syndrome","mondo","0005632"
< "5482","cystadenofibroma","mesh","D062625"
< "5482","cystadenofibroma","umls","C0334317"
< "5482","cystadenofibroma","mondo","0003464"
< "5634","adenosquamous prostate carcinoma","umls","C1335503"
< "5634","adenosquamous prostate carcinoma","mondo","0003558"
< "9455","lipid storage disease","icd10cm","E75.6"
< "9455","lipid storage disease","icd9cm","272.7"
< "9455","lipid storage disease","icd9cm","272.8"
< "9455","lipid storage disease","mesh","D008064"
< "9455","lipid storage disease","umls","C0023794"
< "9455","lipid storage disease","umls","C0029591"
< "9455","lipid storage disease","mondo","0019245"
< "507","adjustment disorder","icd9cm","309"
< "507","adjustment disorder","icd9cm","309.9"
< "507","adjustment disorder","umls","C0040701"
< "507","adjustment disorder","mondo","0003265"
< "9008","psoriatic arthritis","icd10cm","L40.5"
< "9008","psoriatic arthritis","icd10cm","L40.50"
< "9008","psoriatic arthritis","icd9cm","696.0"
< "9008","psoriatic arthritis","mesh","D015535"
< "9008","psoriatic arthritis","umls","C0003872"
< "9008","psoriatic arthritis","mondo","0011849"
---
> "0050876","Caroli disease","mesh","D016767"
> "0050876","Caroli disease","umls","C0162510"
> "0050876","Caroli disease","mondo","0010913"
> "0050873","follicular lymphoma","mesh","D008224"
> "0050873","follicular lymphoma","mondo","0018906"
> "0050871","fibroma","mesh","D005350"
> "0050871","fibroma","mondo","0005167"
> "1039","prolymphocytic leukemia","mesh","D015463"
> "1039","prolymphocytic leukemia","umls","C0023486"
> "1039","prolymphocytic leukemia","mondo","0001023"
> "1036","chronic leukemia","mondo","0001014"
5047,5072c9019,9021
< "633","myositis","icd10cm","G72.49"
< "633","myositis","icd10cm","M60"
< "633","myositis","icd10cm","M60.9"
< "633","myositis","mesh","D009220"
< "633","myositis","umls","C0027121"
< "633","myositis","mondo","0021167"
< "635","acquired immunodeficiency syndrome","icd10cm","B20"
< "635","acquired immunodeficiency syndrome","mesh","D000163"
< "635","acquired immunodeficiency syndrome","umls","C0001175"
< "635","acquired immunodeficiency syndrome","mondo","0012268"
< "636","central pontine myelinolysis","icd10cm","G37.2"
< "636","central pontine myelinolysis","mesh","D017590"
< "636","central pontine myelinolysis","umls","C0206083"
< "636","central pontine myelinolysis","mondo","0006692"
< "639","acute disseminated encephalomyelitis","mesh","D004673"
< "639","acute disseminated encephalomyelitis","umls","C0014059"
< "639","acute disseminated encephalomyelitis","mondo","0019383"
< "1218","echinostomiasis","icd10cm","B66.8"
< "1218","echinostomiasis","mesh","D004451"
< "1218","echinostomiasis","umls","C0013514"
< "1218","echinostomiasis","mondo","0005739"
< "1219","dicrocoeliasis","icd10cm","B66.2"
< "1219","dicrocoeliasis","mesh","D004011"
< "1219","dicrocoeliasis","umls","C0012102"
< "1219","dicrocoeliasis","mondo","0005729"
< "0080093","myofibrillar myopathy 2","mondo","0012130"
---
> "1035","aggressive NK-cell leukemia","icd10cm","C94.8"
> "1035","aggressive NK-cell leukemia","umls","C1292777"
> "1035","aggressive NK-cell leukemia","mondo","0019470"
5079,5093c9028,9042
< "0070143","autosomal recessive cutis laxa type III","mesh","C535990"
< "0070143","autosomal recessive cutis laxa type III","umls","C0268354"
< "0070143","autosomal recessive cutis laxa type III","mondo","0017569"
< "5656","cranial nerve disease","icd10cm","G52.9"
< "5656","cranial nerve disease","icd9cm","352.9"
< "5656","cranial nerve disease","mesh","D003389"
< "5656","cranial nerve disease","umls","C0010266"
< "5656","cranial nerve disease","mondo","0003569"
< "5655","chiasmal syndrome","icd10cm","H47.4"
< "5655","chiasmal syndrome","icd9cm","377.5"
< "5655","chiasmal syndrome","umls","C0155307"
< "5655","chiasmal syndrome","mondo","0003568"
< "7489","Osgood-Schlatter's disease","mesh","D055034"
< "7489","Osgood-Schlatter's disease","umls","C0029376"
< "7489","Osgood-Schlatter's disease","mondo","0004241"
---
> "4372","intracranial embolism","icd10cm","I66"
> "4372","intracranial embolism","icd9cm","434.1"
> "4372","intracranial embolism","mesh","D020766"
> "4372","intracranial embolism","umls","C0007780"
> "4372","intracranial embolism","umls","C0752140"
> "4372","intracranial embolism","mondo","0006809"
> "4370","stomach diverticulosis","mesh","D045724"
> "4370","stomach diverticulosis","umls","C1148546"
> "4370","stomach diverticulosis","mondo","0002976"
> "4371","Schnitzler syndrome","mesh","D019873"
> "4371","Schnitzler syndrome","umls","C0524988"
> "4371","Schnitzler syndrome","mondo","0018304"
> "4376","milk allergy","mesh","D016269"
> "4376","milk allergy","umls","C0079840"
> "4376","milk allergy","mondo","0005849"
5097,5104c9046,9058
< "13593","eclampsia","icd10cm","O15"
< "13593","eclampsia","icd10cm","O15.9"
< "13593","eclampsia","mesh","D004461"
< "13593","eclampsia","umls","C0013537"
< "13593","eclampsia","mondo","0001754"
< "2891","thyroid adenoma","mesh","D013964"
< "2891","thyroid adenoma","umls","C0151468"
< "2891","thyroid adenoma","mondo","0002454"
---
> "4374","silo filler's disease","mesh","D012832"
> "4374","silo filler's disease","umls","C0037120"
> "4374","silo filler's disease","mondo","0006972"
> "14548","steroid-induced glaucoma - borderline","icd9cm","365.03"
> "14548","steroid-induced glaucoma - borderline","umls","C0339572"
> "14548","steroid-induced glaucoma - borderline","mondo","0001996"
> "11060","placenta praevia","icd10cm","O44"
> "11060","placenta praevia","icd10cm","O44.0"
> "11060","placenta praevia","mesh","D010923"
> "11060","placenta praevia","umls","C0032046"
> "11060","placenta praevia","mondo","0005918"
> "14545","seminal vesicle adenocarcinoma","umls","C1519233"
> "14545","seminal vesicle adenocarcinoma","mondo","0001993"
5109,5122c9063,9081
< "2892","exocervical carcinoma","umls","C1299238"
< "2892","exocervical carcinoma","mondo","0002455"
< "1107","esophageal carcinoma","umls","C0152018"
< "1107","esophageal carcinoma","mondo","0019086"
< "4450","renal cell carcinoma","mesh","D002292"
< "4450","renal cell carcinoma","umls","C0007134"
< "4450","renal cell carcinoma","mondo","0005086"
< "4903","granular cell carcinoma","mesh","D000230"
< "4903","granular cell carcinoma","umls","C0205644"
< "4903","granular cell carcinoma","mondo","0003197"
< "0110672","congenital myasthenic syndrome 21","mondo","0014983"
< "686","liver carcinoma","umls","C0279000"
< "686","liver carcinoma","mondo","0007256"
< "0070071","autosomal dominant non-syndromic intellectual disability 41","mondo","0014842"
---
> "14546","sphenoidal sinus cancer","icd10cm","C31.3"
> "14546","sphenoidal sinus cancer","icd9cm","160.5"
> "14546","sphenoidal sinus cancer","umls","C0153479"
> "14546","sphenoidal sinus cancer","mondo","0001994"
> "8660","postcricoid region cancer","icd10cm","C13.0"
> "8660","postcricoid region cancer","icd9cm","148.0"
> "8660","postcricoid region cancer","umls","C0496769"
> "8660","postcricoid region cancer","mondo","0004635"
> "8661","lip carcinoma in situ","icd10cm","D00.0"
> "8661","lip carcinoma in situ","icd9cm","230.0"
> "8661","lip carcinoma in situ","umls","C0154058"
> "8661","lip carcinoma in situ","mondo","0004636"
> "8663","aryepiglottic fold cancer","icd10cm","C13.1"
> "8663","aryepiglottic fold cancer","icd9cm","148.2"
> "8663","aryepiglottic fold cancer","umls","C0153401"
> "8663","aryepiglottic fold cancer","mondo","0004637"
> "4080","tricuspid valve insufficiency","mesh","D014262"
> "4080","tricuspid valve insufficiency","umls","C0040961"
> "4080","tricuspid valve insufficiency","mondo","0002870"
5131,5134c9090,9093
< "0060731","congenital central hypoventilation syndrome","icd10cm","G47.3"
< "0060731","congenital central hypoventilation syndrome","mondo","0008852"
< "0060730","torsion dystonia 1","icd10cm","G24.1"
< "0060730","torsion dystonia 1","mondo","0007492"
---
> "4086","testicular germ cell tumor non-seminomatous","umls","C1336724"
> "4086","testicular germ cell tumor non-seminomatous","mondo","0006447"
> "4087","testicular pure germ cell tumor","umls","C1514608"
> "4087","testicular pure germ cell tumor","mondo","0002874"
5143,5150c9102,9111
< "8408","Meckel's diverticulitis","umls","C0267497"
< "8408","Meckel's diverticulitis","mondo","0004551"
< "8584","Burkitt lymphoma","icd10cm","C83.7"
< "8584","Burkitt lymphoma","icd10cm","C83.70"
< "8584","Burkitt lymphoma","icd9cm","200.2"
< "8584","Burkitt lymphoma","mesh","D002051"
< "8584","Burkitt lymphoma","umls","C0006413"
< "8584","Burkitt lymphoma","mondo","0007243"
---
> "11320","Kyasanur forest disease","icd10cm","A98.2"
> "11320","Kyasanur forest disease","icd9cm","065.2"
> "11320","Kyasanur forest disease","mesh","D007733"
> "11320","Kyasanur forest disease","umls","C0022810"
> "11320","Kyasanur forest disease","mondo","0017881"
> "11328","schizophreniform disorder","icd10cm","F20.81"
> "11328","schizophreniform disorder","icd9cm","295.4"
> "11328","schizophreniform disorder","mesh","D011618"
> "11328","schizophreniform disorder","umls","C0036358"
> "11328","schizophreniform disorder","mondo","0001265"
5156,5160d9116
< "1455","geographic tongue","icd10cm","K14.1"
< "1455","geographic tongue","icd9cm","529.1"
< "1455","geographic tongue","mesh","D005929"
< "1455","geographic tongue","umls","C0017677"
< "1455","geographic tongue","mondo","0005771"
5165,5173c9121,9129
< "0110400","retinitis pigmentosa 22","icd10cm","H35.5"
< "0110400","retinitis pigmentosa 22","mondo","0011259"
< "7578","breast scirrhous carcinoma","umls","C0346151"
< "7578","breast scirrhous carcinoma","mondo","0004288"
< "9746","hemorrhoid","icd10cm","K64"
< "9746","hemorrhoid","icd9cm","455"
< "9746","hemorrhoid","mesh","D006484"
< "9746","hemorrhoid","umls","C0019112"
< "9746","hemorrhoid","mondo","0004872"
---
> "5723","optic atrophy","icd10cm","H47.2"
> "5723","optic atrophy","icd10cm","H47.20"
> "5723","optic atrophy","icd9cm","377.1"
> "5723","optic atrophy","icd9cm","377.10"
> "5723","optic atrophy","mesh","D009896"
> "5723","optic atrophy","umls","C0029124"
> "5723","optic atrophy","mondo","0003608"
> "5726","uterine ligament papillary cystadenoma","umls","C3642324"
> "5726","uterine ligament papillary cystadenoma","mondo","0003611"
5176,5294c9132,9156
< "1891","optic nerve disease","mesh","D009901"
< "1891","optic nerve disease","umls","C0029132"
< "1891","optic nerve disease","mondo","0002135"
< "3185","spinal cord glioma","umls","C2937245"
< "3185","spinal cord glioma","mondo","0002542"
< "0110670","congenital myasthenic syndrome 9","mondo","0014587"
< "4923","thymus adenocarcinoma","umls","C1336743"
< "4923","thymus adenocarcinoma","mondo","0003209"
< "3910","lung adenocarcinoma","mesh","C538231"
< "3910","lung adenocarcinoma","umls","C0152013"
< "3910","lung adenocarcinoma","umls","C1335060"
< "3910","lung adenocarcinoma","mondo","0005061"
< "0110708","hypotrichosis 11","mondo","0014027"
< "0110709","hypotrichosis 12","mondo","0014384"
< "8310","sclerosing adenosis of breast","umls","C1335931"
< "8310","sclerosing adenosis of breast","mondo","0004531"
< "0110878","holoprosencephaly 5","mondo","0012322"
< "0110838","Usher syndrome type 2A","icd10cm","H35.5"
< "0110838","Usher syndrome type 2A","mondo","0010169"
< "0090124","neurogenic arthrogryposis multiplex congenita","mesh","C536614"
< "0090124","neurogenic arthrogryposis multiplex congenita","umls","C1859721"
< "0090124","neurogenic arthrogryposis multiplex congenita","mondo","0008823"
< "3070","malignant glioma","kegg","05214"
< "3070","malignant glioma","mesh","D005910"
< "3070","malignant glioma","umls","C0017638"
< "3070","malignant glioma","umls","C0555198"
< "3070","malignant glioma","mondo","0015917"
< "4153","spinal chordoma","mondo","0002894"
< "4151","skull base chordoma","umls","C1335975"
< "4151","skull base chordoma","mondo","0002892"
< "4156","primary syphilis","icd9cm","091"
< "4156","primary syphilis","umls","C0153139"
< "4156","primary syphilis","mondo","0002896"
< "4157","secondary syphilis","icd9cm","091.9"
< "4157","secondary syphilis","mesh","C536773"
< "4157","secondary syphilis","umls","C0149985"
< "4157","secondary syphilis","mondo","0002897"
< "11258","cat-scratch disease","icd10cm","A28.1"
< "11258","cat-scratch disease","icd9cm","078.3"
< "11258","cat-scratch disease","mesh","D002372"
< "11258","cat-scratch disease","umls","C0007361"
< "11258","cat-scratch disease","mondo","0005692"
< "5831","fallopian tube endometrioid adenocarcinoma","umls","C1333592"
< "5831","fallopian tube endometrioid adenocarcinoma","umls","C1517113"
< "5831","fallopian tube endometrioid adenocarcinoma","mondo","0003666"
< "11256","typhus","icd10cm","A75"
< "11256","typhus","icd10cm","A75.0"
< "11256","typhus","icd10cm","A75.2"
< "11256","typhus","icd10cm","A75.9"
< "11256","typhus","icd9cm","080"
< "11256","typhus","icd9cm","081.0"
< "11256","typhus","icd9cm","081.9"
< "11256","typhus","mesh","D014437"
< "11256","typhus","mesh","D014438"
< "11256","typhus","umls","C0041471"
< "11256","typhus","umls","C0041472"
< "11256","typhus","umls","C0041473"
< "11256","typhus","mondo","0001246"
< "11254","Brill-Zinsser disease","icd10cm","A75.1"
< "11254","Brill-Zinsser disease","icd9cm","081.1"
< "11254","Brill-Zinsser disease","mesh","D014438"
< "11254","Brill-Zinsser disease","umls","C0006181"
< "11254","Brill-Zinsser disease","mondo","0005680"
< "0090126","branched-chain keto acid dehydrogenase kinase deficiency","icd10cm","E71.1"
< "0090126","branched-chain keto acid dehydrogenase kinase deficiency","mondo","0013970"
< "8869","neuromyelitis optica","icd10cm","G36.0"
< "8869","neuromyelitis optica","icd9cm","341.0"
< "8869","neuromyelitis optica","mesh","D009471"
< "8869","neuromyelitis optica","umls","C0027873"
< "8869","neuromyelitis optica","mondo","0019100"
< "0110874","holoprosencephaly 6","mondo","0011616"
< "0110703","hypotrichosis 6","mondo","0011932"
< "0110839","Usher syndrome type 2C","icd10cm","H35.5"
< "0110839","Usher syndrome type 2C","mondo","0011558"
< "4810","cerebrotendinous xanthomatosis","mesh","D019294"
< "4810","cerebrotendinous xanthomatosis","umls","C0238052"
< "4810","cerebrotendinous xanthomatosis","mondo","0008948"
< "4929","tubular adenocarcinoma","mesh","D000230"
< "4929","tubular adenocarcinoma","umls","C0205645"
< "4929","tubular adenocarcinoma","mondo","0005606"
< "0080173","bladder exstrophy-epispadias-cloacal exstrophy complex","mondo","0017919"
< "0080172","thiopurine S-methyltransferase deficiency","mondo","0012503"
< "0080171","esophageal atresia/tracheoesophageal fistula","mondo","0008586"
< "0110877","holoprosencephaly 11","mondo","0013642"
< "0080177","hepatic veno-occlusive disease","icd10cm","K76.5"
< "0080177","hepatic veno-occlusive disease","mesh","D006504"
< "0080177","hepatic veno-occlusive disease","mondo","0019514"
< "0060848","early infantile epileptic encephalopathy 9","mondo","0010246"
< "4080","tricuspid valve insufficiency","mesh","D014262"
< "4080","tricuspid valve insufficiency","umls","C0040961"
< "4080","tricuspid valve insufficiency","mondo","0002870"
< "0060844","Norrie disease","mesh","C537849"
< "0060844","Norrie disease","umls","C0266526"
< "0060844","Norrie disease","mondo","0010691"
< "0060841","isolated microphthalmia 8","icd10cm","Q11.0"
< "0060841","isolated microphthalmia 8","mondo","0014050"
< "0060840","isolated microphthalmia 1","icd10cm","Q11.0"
< "0060840","isolated microphthalmia 1","mondo","0009631"
< "0060843","hereditary neuropathy with liability to pressure palsies","mesh","C536965"
< "0060843","hereditary neuropathy with liability to pressure palsies","umls","C0393814"
< "0060843","hereditary neuropathy with liability to pressure palsies","mondo","0008087"
< "0110707","hypotrichosis 10","mondo","0013650"
< "0110704","hypotrichosis 7","mondo","0011452"
< "6088","acute stress disorder","icd9cm","308.3"
< "6088","acute stress disorder","umls","C0029488"
< "6088","acute stress disorder","mondo","0003763"
< "6084","pediatric ovarian germ cell tumor","umls","C0796664"
< "6084","pediatric ovarian germ cell tumor","mondo","0003760"
< "0110873","holoprosencephaly 9","mondo","0012563"
< "6083","childhood ovarian endodermal sinus tumor","umls","C1332993"
< "6083","childhood ovarian endodermal sinus tumor","mondo","0003759"
< "0111095","Fanconi anemia complementation group A","mondo","0009215"
< "884","metagonimiasis","icd10cm","B66.8"
< "884","metagonimiasis","icd9cm","121.5"
< "884","metagonimiasis","mesh","D014201"
< "884","metagonimiasis","umls","C0025530"
< "884","metagonimiasis","mondo","0004666"
< "5999","apocrine adenosis of breast","umls","C1332314"
< "5999","apocrine adenosis of breast","mondo","0003726"
---
> "5724","seminal vesicle cystadenoma","umls","C1519234"
> "5724","seminal vesicle cystadenoma","mondo","0003609"
> "5725","rete ovarii cystadenoma","umls","C1514907"
> "5725","rete ovarii cystadenoma","mondo","0003610"
> "0110837","Usher syndrome type 1K","icd10cm","H35.5"
> "0110837","Usher syndrome type 1K","mondo","0014001"
> "11491","acquired night blindness","icd10cm","H53.62"
> "11491","acquired night blindness","icd9cm","368.62"
> "11491","acquired night blindness","umls","C0152202"
> "11491","acquired night blindness","mondo","0001296"
> "8081","myxomatous pattern testicular yolk sac tumor","umls","C1515309"
> "8081","myxomatous pattern testicular yolk sac tumor","mondo","0004453"
> "8082","cellular congenital mesoblastic nephroma","umls","C1516474"
> "8082","cellular congenital mesoblastic nephroma","mondo","0004454"
> "8083","classic congenital mesoblastic nephroma","umls","C1516475"
> "8083","classic congenital mesoblastic nephroma","mondo","0004455"
> "14032","malignant parietal pleura tumor","umls","C0153495"
> "14032","malignant parietal pleura tumor","mondo","0001861"
> "6648","adult pineoblastoma","umls","C0281332"
> "6648","adult pineoblastoma","mondo","0003957"
> "12678","hypercalcemia","icd10cm","E83.52"
> "12678","hypercalcemia","icd9cm","275.42"
> "12678","hypercalcemia","mesh","D006934"
> "12678","hypercalcemia","umls","C0020437"
> "12678","hypercalcemia","mondo","0001566"
5296a9159,9167
> "6643","Baastrup's syndrome","icd10cm","M48.2"
> "6643","Baastrup's syndrome","icd10cm","M48.20"
> "6643","Baastrup's syndrome","icd9cm","721.5"
> "6643","Baastrup's syndrome","umls","C0158248"
> "6643","Baastrup's syndrome","mondo","0003956"
> "10813","nasal cavity lymphoma","umls","C1334921"
> "10813","nasal cavity lymphoma","mondo","0001130"
> "10812","nasal cavity olfactory neuroblastoma","umls","C1334923"
> "10812","nasal cavity olfactory neuroblastoma","mondo","0001129"
5301,5304c9172,9179
< "11725","Cornelia de Lange syndrome","icd10cm","Q87.1"
< "11725","Cornelia de Lange syndrome","mesh","D003635"
< "11725","Cornelia de Lange syndrome","umls","C0270972"
< "11725","Cornelia de Lange syndrome","mondo","0016033"
---
> "10810","tibialis tendinitis","icd9cm","726.72"
> "10810","tibialis tendinitis","umls","C0158321"
> "10810","tibialis tendinitis","mondo","0001127"
> "10817","sexual sadism","icd10cm","F65.52"
> "10817","sexual sadism","icd9cm","302.84"
> "10817","sexual sadism","mesh","D012448"
> "10817","sexual sadism","umls","C0036913"
> "10817","sexual sadism","mondo","0001132"
5307,5333c9182,9187
< "0110505","autosomal recessive nonsyndromic deafness 48","icd10cm","H90.3"
< "0110505","autosomal recessive nonsyndromic deafness 48","mondo","0012273"
< "0111091","Fanconi anemia complementation group I","mondo","0012186"
< "11723","Duchenne muscular dystrophy","mesh","D020388"
< "11723","Duchenne muscular dystrophy","umls","C0013264"
< "11723","Duchenne muscular dystrophy","mondo","0010679"
< "0050471","Carney complex","mesh","D056733"
< "0050471","Carney complex","umls","C0406810"
< "0050471","Carney complex","umls","C1854540"
< "0050471","Carney complex","umls","C2607929"
< "0050471","Carney complex","mondo","0015285"
< "0050470","Donohue syndrome","mesh","D056731"
< "0050470","Donohue syndrome","umls","C0265344"
< "0050470","Donohue syndrome","umls","C0271695"
< "0050470","Donohue syndrome","mondo","0009517"
< "0050477","Liddle syndrome","mesh","D056929"
< "0050477","Liddle syndrome","umls","C0221043"
< "0050477","Liddle syndrome","mondo","0008323"
< "0050476","Barth syndrome","icd10cm","E78.71"
< "0050476","Barth syndrome","mesh","D056889"
< "0050476","Barth syndrome","umls","C0574083"
< "0050476","Barth syndrome","mondo","0010543"
< "0050475","Weill-Marchesani syndrome","mesh","D056846"
< "0050475","Weill-Marchesani syndrome","umls","C0265313"
< "0050475","Weill-Marchesani syndrome","umls","C1869114"
< "0050475","Weill-Marchesani syndrome","umls","C1869115"
< "0050475","Weill-Marchesani syndrome","mondo","0018096"
---
> "0070039","autosomal dominant non-syndromic intellectual disability 9","mondo","0013656"
> "0070038","autosomal dominant non-syndromic intellectual disability 8","mondo","0013655"
> "7807","choroid necrotic melanoma","umls","C1333026"
> "7807","choroid necrotic melanoma","mondo","0004364"
> "7806","adult spinal cord glioblastoma multiforme","umls","C0559185"
> "7806","adult spinal cord glioblastoma multiforme","mondo","0004363"
5335c9189,9190
< "0070034","autosomal dominant non-syndromic intellectual disability 4","mondo","0012947"
---
> "7808","necrotic uveal melanoma","umls","C1334931"
> "7808","necrotic uveal melanoma","mondo","0004365"
5342,5392d9196
< "13413","hepatic encephalopathy","icd10cm","K72"
< "13413","hepatic encephalopathy","icd9cm","572.2"
< "13413","hepatic encephalopathy","mesh","D006501"
< "13413","hepatic encephalopathy","umls","C0019151"
< "13413","hepatic encephalopathy","mondo","0001711"
< "0060296","congenital secretory chloride diarrhea 1","mesh","C536210"
< "0060296","congenital secretory chloride diarrhea 1","umls","C0267662"
< "0060296","congenital secretory chloride diarrhea 1","mondo","0008964"
< "3649","pyruvate decarboxylase deficiency","icd10cm","E74.4"
< "3649","pyruvate decarboxylase deficiency","mesh","D015325"
< "3649","pyruvate decarboxylase deficiency","umls","C0034345"
< "3649","pyruvate decarboxylase deficiency","mondo","0019169"
< "6050","esophageal disease","icd10cm","K22.9"
< "6050","esophageal disease","icd9cm","530"
< "6050","esophageal disease","icd9cm","530.9"
< "6050","esophageal disease","mesh","D004935"
< "6050","esophageal disease","umls","C0014852"
< "6050","esophageal disease","mondo","0003749"
< "3640","central nervous system teratoma","umls","C1332895"
< "3640","central nervous system teratoma","mondo","0002718"
< "0111103","maturity-onset diabetes of the young type 4","mondo","0011667"
< "0090010","immunodeficiency-centromeric instability-facial anomalies syndrome 3","icd10cm","D84.8"
< "0090010","immunodeficiency-centromeric instability-facial anomalies syndrome 3","mondo","0014828"
< "0090013","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive","icd10cm","D81.1"
< "0090013","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive","mondo","0011086"
< "0111100","maturity-onset diabetes of the young type 2","mondo","0007453"
< "0090015","Cenani-Lenz syndactyly syndrome","icd10cm","Q78.4"
< "0090015","Cenani-Lenz syndactyly syndrome","mondo","0008931"
< "0111106","maturity-onset diabetes of the young type 7","mondo","0012513"
< "0090017","epidermolysis bullosa simplex with muscular dystrophy","icd10cm","Q81.0"
< "0090017","epidermolysis bullosa simplex with muscular dystrophy","mondo","0009181"
< "0090016","chromosome 5q deletion syndrome","icd10cm","D46.7"
< "0090016","chromosome 5q deletion syndrome","mondo","0007925"
< "11678","onchocerciasis","icd10cm","B73"
< "11678","onchocerciasis","icd9cm","125.3"
< "11678","onchocerciasis","mesh","D009855"
< "11678","onchocerciasis","umls","C0029001"
< "11678","onchocerciasis","mondo","0017137"
< "2559","opiate dependence","icd10cm","F11.2"
< "2559","opiate dependence","icd9cm","304.0"
< "2559","opiate dependence","icd9cm","304.00"
< "2559","opiate dependence","mesh","D009293"
< "2559","opiate dependence","umls","C0524662"
< "2559","opiate dependence","mondo","0005530"
< "0111109","maturity-onset diabetes of the young type 11","mondo","0013242"
< "0111108","maturity-onset diabetes of the young type 10","mondo","0013240"
< "3007","breast ductal carcinoma","mesh","D044584"
< "3007","breast ductal carcinoma","umls","C1176475"
< "3007","breast ductal carcinoma","mondo","0005590"
< "0111151","Prinzmetal angina","mesh","D000788"
< "0111151","Prinzmetal angina","mondo","0006021"
5400,5453c9204,9205
< "0060197","amyotrophic lateral sclerosis type 5","mondo","0011196"
< "12783","migraine without aura","icd10cm","G43.0"
< "12783","migraine without aura","icd10cm","G43.009"
< "12783","migraine without aura","icd9cm","346.1"
< "12783","migraine without aura","mesh","D020326"
< "12783","migraine without aura","umls","C0338480"
< "12783","migraine without aura","mondo","0011847"
< "0090106","Bh4-deficient hyperphenylalaninemia A","mesh","C535325"
< "0090106","Bh4-deficient hyperphenylalaninemia A","umls","C0878676"
< "0090106","Bh4-deficient hyperphenylalaninemia A","mondo","0009863"
< "4717","extragonadal germ cell cancer","umls","C0262963"
< "4717","extragonadal germ cell cancer","umls","C1334581"
< "4717","extragonadal germ cell cancer","mondo","0003113"
< "10322","berylliosis","icd10cm","J63.2"
< "10322","berylliosis","mesh","D001607"
< "10322","berylliosis","umls","C0005138"
< "10322","berylliosis","mondo","0015274"
< "10325","silicosis","icd10cm","J62"
< "10325","silicosis","icd10cm","J62.8"
< "10325","silicosis","icd9cm","502"
< "10325","silicosis","mesh","D012829"
< "10325","silicosis","umls","C0037116"
< "10325","silicosis","mondo","0005960"
< "14305","tuberculous empyema","mesh","D004654"
< "14305","tuberculous empyema","umls","C0014014"
< "14305","tuberculous empyema","mondo","0005999"
< "0050699","Dent disease","mesh","C538212"
< "0050699","Dent disease","mesh","C564487"
< "0050699","Dent disease","mesh","D057973"
< "0050699","Dent disease","umls","C0878681"
< "0050699","Dent disease","umls","C1845167"
< "0050699","Dent disease","umls","C1848336"
< "0050699","Dent disease","mondo","0015612"
< "10326","Caplan's syndrome","mesh","D002205"
< "10326","Caplan's syndrome","umls","C0006915"
< "10326","Caplan's syndrome","mondo","0005690"
< "4893","middle ear carcinoma","umls","C1334760"
< "4893","middle ear carcinoma","mondo","0003190"
< "4892","middle ear adenocarcinoma","umls","C1334758"
< "4892","middle ear adenocarcinoma","mondo","0003189"
< "2772","irritant dermatitis","icd10cm","L24"
< "2772","irritant dermatitis","icd10cm","L24.9"
< "2772","irritant dermatitis","mesh","D017453"
< "2772","irritant dermatitis","umls","C0162823"
< "2772","irritant dermatitis","mondo","0006564"
< "3002","ovary neuroendocrine neoplasm","umls","C1335172"
< "3002","ovary neuroendocrine neoplasm","mondo","0002481"
< "0050690","brachyolmia","mondo","0015262"
< "2256","osteochondrodysplasia","icd10cm","Q78.9"
< "2256","osteochondrodysplasia","icd9cm","756.4"
< "2256","osteochondrodysplasia","mesh","D010009"
< "2256","osteochondrodysplasia","umls","C0008449"
< "2256","osteochondrodysplasia","umls","C0029422"
< "2256","osteochondrodysplasia","mondo","0005516"
---
> "2392","glandular cystitis","umls","C0268837"
> "2392","glandular cystitis","mondo","0002287"
5455,5496c9207,9245
< "0060896","autosomal recessive early-onset Parkinson's disease 23","icd10cm","G20"
< "0060896","autosomal recessive early-onset Parkinson's disease 23","mondo","0014796"
< "0070100","oculocutaneous albinism type VII","mondo","0014070"
< "0090105","autosomal recessive hypercholesterolemia","icd10cm","E78.0"
< "0090105","autosomal recessive hypercholesterolemia","mondo","0011374"
< "9146","visceral leishmaniasis","icd10cm","B55.0"
< "9146","visceral leishmaniasis","icd9cm","085.0"
< "9146","visceral leishmaniasis","mesh","D007898"
< "9146","visceral leishmaniasis","umls","C0023290"
< "9146","visceral leishmaniasis","mondo","0005445"
< "5165","uterine corpus sarcoma","umls","C0338113"
< "5165","uterine corpus sarcoma","mondo","0005210"
< "0110746","type 1 diabetes mellitus 7","icd10cm","E10"
< "0110746","type 1 diabetes mellitus 7","mondo","0010864"
< "0110747","type 1 diabetes mellitus 8","icd10cm","E10"
< "0110747","type 1 diabetes mellitus 8","mondo","0010950"
< "0110744","type 1 diabetes mellitus 5","icd10cm","E10"
< "0110744","type 1 diabetes mellitus 5","mondo","0010863"
< "0110745","type 1 diabetes mellitus 6","icd10cm","E10"
< "0110745","type 1 diabetes mellitus 6","mondo","0011167"
< "6262","follicular dendritic cell sarcoma","icd10cm","C96.4"
< "6262","follicular dendritic cell sarcoma","mesh","D054740"
< "6262","follicular dendritic cell sarcoma","umls","C1260325"
< "6262","follicular dendritic cell sarcoma","mondo","0005764"
< "0110743","type 1 diabetes mellitus 4","icd10cm","E10"
< "0110743","type 1 diabetes mellitus 4","mondo","0010862"
< "0110740","neurodegeneration with brain iron accumulation 6","icd10cm","G23.0"
< "0110740","neurodegeneration with brain iron accumulation 6","mondo","0014290"
< "0110741","type 1 diabetes mellitus 2","icd10cm","E10"
< "0110741","type 1 diabetes mellitus 2","mondo","0007454"
< "12259","hemophilia B","icd10cm","D67"
< "12259","hemophilia B","icd9cm","286.1"
< "12259","hemophilia B","mesh","D002836"
< "12259","hemophilia B","umls","C0008533"
< "12259","hemophilia B","mondo","0010604"
< "0110749","type 1 diabetes mellitus 10","icd10cm","E10"
< "0110749","type 1 diabetes mellitus 10","mondo","0011168"
< "2640","struma ovarii","mesh","D013330"
< "2640","struma ovarii","umls","C0038478"
< "2640","struma ovarii","mondo","0006980"
< "0110742","type 1 diabetes mellitus 3","icd10cm","E10"
< "0110742","type 1 diabetes mellitus 3","mondo","0010861"
---
> "0050508","variola major","icd9cm","050.0"
> "0050508","variola major","umls","C1812609"
> "0050508","variola major","mondo","0000338"
> "1858","McCune Albright syndrome","icd10cm","Q78.1"
> "1858","McCune Albright syndrome","icd9cm","756.54"
> "1858","McCune Albright syndrome","mesh","D005357"
> "1858","McCune Albright syndrome","mesh","D005359"
> "1858","McCune Albright syndrome","umls","C0016063"
> "1858","McCune Albright syndrome","umls","C0016065"
> "1858","McCune Albright syndrome","mondo","0018919"
> "5693","adult liposarcoma","umls","C0278608"
> "5693","adult liposarcoma","mondo","0003585"
> "1852","intrahepatic cholestasis","mesh","D002780"
> "1852","intrahepatic cholestasis","umls","C0008372"
> "1852","intrahepatic cholestasis","mondo","0019072"
> "3843","diencephalic neoplasm","umls","C1333286"
> "3843","diencephalic neoplasm","umls","C1334576"
> "3843","diencephalic neoplasm","mondo","0002786"
> "1856","cherubism","icd10cm","M27.8"
> "1856","cherubism","mesh","D002636"
> "1856","cherubism","umls","C0008029"
> "1856","cherubism","mondo","0007315"
> "2173","eyelid benign neoplasm","mesh","D005142"
> "2173","eyelid benign neoplasm","umls","C0015424"
> "2173","eyelid benign neoplasm","mondo","0002235"
> "2170","vaginitis","icd9cm","616.1"
> "2170","vaginitis","icd9cm","616.10"
> "2170","vaginitis","mesh","D014627"
> "2170","vaginitis","umls","C0042267"
> "2170","vaginitis","umls","C0042268"
> "2170","vaginitis","mondo","0002234"
> "5691","visual cortex disease","icd10cm","H47.6"
> "5691","visual cortex disease","icd9cm","377.7"
> "5691","visual cortex disease","umls","C0234398"
> "5691","visual cortex disease","mondo","0003584"
> "2176","carbuncle","icd9cm","680.9"
> "2176","carbuncle","mesh","D002270"
> "2176","carbuncle","umls","C0007079"
> "2176","carbuncle","mondo","0002237"
5502,5504c9251,9254
< "4078","tricuspid valve stenosis","mesh","D014264"
< "4078","tricuspid valve stenosis","umls","C0040963"
< "4078","tricuspid valve stenosis","mondo","0005997"
---
> "4968","Nelson syndrome","icd10cm","E24.1"
> "4968","Nelson syndrome","mesh","D009347"
> "4968","Nelson syndrome","umls","C0027577"
> "4968","Nelson syndrome","mondo","0016035"
5518,5522c9268,9270
< "4333","parovarian cyst","icd10cm","Q50.4"
< "4333","parovarian cyst","icd10cm","Q50.5"
< "4333","parovarian cyst","mesh","D010310"
< "4333","parovarian cyst","umls","C0030584"
< "4333","parovarian cyst","mondo","0002965"
---
> "4961","bone marrow disease","mesh","D001855"
> "4961","bone marrow disease","umls","C0005956"
> "4961","bone marrow disease","mondo","0003225"
5527,5536c9275,9291
< "0110680","congenital myasthenic syndrome 2C","mondo","0014582"
< "2600","laryngeal carcinoma","umls","C0595989"
< "2600","laryngeal carcinoma","mondo","0002358"
< "8224","central breast papilloma","umls","C1332896"
< "8224","central breast papilloma","mondo","0004505"
< "2602","chondroma","mesh","D002812"
< "2602","chondroma","umls","C0936248"
< "2602","chondroma","mondo","0002360"
< "0110981","Joubert syndrome 10","mesh","C567582"
< "0110981","Joubert syndrome 10","mondo","0010431"
---
> "14040","autoimmune polyendocrine syndrome","icd10cm","E31.0"
> "14040","autoimmune polyendocrine syndrome","mesh","D016884"
> "14040","autoimmune polyendocrine syndrome","umls","C0085409"
> "14040","autoimmune polyendocrine syndrome","mondo","0017278"
> "3847","papillary craniopharyngioma","mesh","D003397"
> "3847","papillary craniopharyngioma","umls","C0431128"
> "3847","papillary craniopharyngioma","mondo","0002788"
> "14042","bipolar I disorder","icd9cm","296.50"
> "14042","bipolar I disorder","umls","C0236773"
> "14042","bipolar I disorder","mondo","0001866"
> "14043","neonatal myasthenia gravis","icd9cm","775.2"
> "14043","neonatal myasthenia gravis","mesh","D020941"
> "14043","neonatal myasthenia gravis","umls","C0158982"
> "14043","neonatal myasthenia gravis","mondo","0006866"
> "3846","adamantinous craniopharyngioma","mesh","D003397"
> "3846","adamantinous craniopharyngioma","umls","C0431129"
> "3846","adamantinous craniopharyngioma","mondo","0002787"
5539,5542c9294,9303
< "0070215","familial hyperinsulinemic hypoglycemia 4","mondo","0012382"
< "0070214","familial hyperinsulinemic hypoglycemia 7","umls","C1864902"
< "0070214","familial hyperinsulinemic hypoglycemia 7","mondo","0012396"
< "0070217","familial hyperinsulinemic hypoglycemia 6","mondo","0011717"
---
> "3261","hyper IgE recurrent infection syndrome 1","mesh","D007589"
> "3261","hyper IgE recurrent infection syndrome 1","umls","C1968689"
> "3261","hyper IgE recurrent infection syndrome 1","umls","C2936739"
> "3261","hyper IgE recurrent infection syndrome 1","mondo","0007818"
> "3260","spindle cell rhabdomyosarcoma","umls","C1266134"
> "3260","spindle cell rhabdomyosarcoma","mondo","0002581"
> "3263","piebaldism","icd10cm","E70.39"
> "3263","piebaldism","mesh","D016116"
> "3263","piebaldism","umls","C0080024"
> "3263","piebaldism","mondo","0008244"
5546,5562c9307,9318
< "10039","late congenital syphilis","icd10cm","A50.4"
< "10039","late congenital syphilis","icd10cm","A50.40"
< "10039","late congenital syphilis","icd10cm","A50.5"
< "10039","late congenital syphilis","icd10cm","A50.59"
< "10039","late congenital syphilis","icd9cm","090.4"
< "10039","late congenital syphilis","icd9cm","090.40"
< "10039","late congenital syphilis","icd9cm","090.5"
< "10039","late congenital syphilis","mesh","D009494"
< "10039","late congenital syphilis","umls","C0153132"
< "10039","late congenital syphilis","umls","C0153136"
< "10039","late congenital syphilis","mondo","0005821"
< "0070210","hereditary lymphedema IA","mondo","0007919"
< "0070213","hereditary lymphedema II","umls","C0238261"
< "0070213","hereditary lymphedema II","umls","C1704424"
< "0070213","hereditary lymphedema II","umls","C1704425"
< "0070213","hereditary lymphedema II","mondo","0007920"
< "0070212","hereditary lymphedema I","umls","C1704423"
---
> "3265","chronic granulomatous disease","icd10cm","D71"
> "3265","chronic granulomatous disease","mesh","D006105"
> "3265","chronic granulomatous disease","umls","C0018203"
> "3265","chronic granulomatous disease","mondo","0018305"
> "5129","simple partial epilepsy","icd9cm","345.51"
> "5129","simple partial epilepsy","umls","C0154712"
> "5129","simple partial epilepsy","mondo","0003290"
> "3267","mucinous ovarian cystadenoma","umls","C0346172"
> "3267","mucinous ovarian cystadenoma","mondo","0002583"
> "1934","dysostosis","mesh","D004413"
> "1934","dysostosis","umls","C0013393"
> "1934","dysostosis","mondo","0018234"
5571,5572d9326
< "0070219","familial hyperinsulinemic hypoglycemia 1","mondo","0009734"
< "0070218","familial hyperinsulinemic hypoglycemia 2","mondo","0011153"
5575,5615c9329,9336
< "0110522","autosomal recessive nonsyndromic deafness 71","icd10cm","H90.3"
< "0110522","autosomal recessive nonsyndromic deafness 71","mondo","0013010"
< "0110523","autosomal recessive nonsyndromic deafness 74","icd10cm","H90.3"
< "0110523","autosomal recessive nonsyndromic deafness 74","mondo","0013386"
< "845","cyclothymic disorder","icd10cm","F34.0"
< "845","cyclothymic disorder","icd9cm","301.1"
< "845","cyclothymic disorder","icd9cm","301.10"
< "845","cyclothymic disorder","icd9cm","301.13"
< "845","cyclothymic disorder","mesh","D003527"
< "845","cyclothymic disorder","umls","C0010598"
< "845","cyclothymic disorder","mondo","0004572"
< "0110521","autosomal recessive nonsyndromic deafness 70","icd10cm","H90.3"
< "0110521","autosomal recessive nonsyndromic deafness 70","mondo","0013978"
< "0110526","autosomal recessive nonsyndromic deafness 79","icd10cm","H90.3"
< "0110526","autosomal recessive nonsyndromic deafness 79","mondo","0013215"
< "0110527","autosomal recessive nonsyndromic deafness 8","icd10cm","H90.3"
< "0110527","autosomal recessive nonsyndromic deafness 8","mondo","0010987"
< "841","extrinsic allergic alveolitis","icd10cm","J67.9"
< "841","extrinsic allergic alveolitis","icd9cm","495"
< "841","extrinsic allergic alveolitis","icd9cm","495.9"
< "841","extrinsic allergic alveolitis","mesh","D000542"
< "841","extrinsic allergic alveolitis","umls","C0002390"
< "841","extrinsic allergic alveolitis","mondo","0004553"
< "840","cork-handlers' disease","icd10cm","J67.3"
< "840","cork-handlers' disease","icd9cm","495.3"
< "840","cork-handlers' disease","umls","C0152108"
< "840","cork-handlers' disease","mondo","0004549"
< "0110528","autosomal recessive nonsyndromic deafness 83","icd10cm","H90.3"
< "0110528","autosomal recessive nonsyndromic deafness 83","mondo","0013365"
< "0110529","autosomal recessive nonsyndromic deafness 84A","icd10cm","H90.3"
< "0110529","autosomal recessive nonsyndromic deafness 84A","mondo","0013249"
< "0110437","dilated cardiomyopathy 1K","icd10cm","I42.0"
< "0110437","dilated cardiomyopathy 1K","mondo","0011567"
< "849","rheumatoid arthritis interstitial lung disease","icd9cm","714.81"
< "849","rheumatoid arthritis interstitial lung disease","mondo","0004586"
< "848","arthritis","icd10cm","M19.90"
< "848","arthritis","mesh","D001168"
< "848","arthritis","umls","C0003864"
< "848","arthritis","mondo","0005578"
< "4902","appendix carcinoma","umls","C0728951"
< "4902","appendix carcinoma","mondo","0003196"
---
> "9191","diabetic macular edema","icd9cm","362.07"
> "9191","diabetic macular edema","umls","C0730285"
> "9191","diabetic macular edema","mondo","0004728"
> "7945","adult central nervous system mixed germ cell tumor","umls","C1332195"
> "7945","adult central nervous system mixed germ cell tumor","mondo","0004406"
> "1426","ureteral disease","mesh","D014515"
> "1426","ureteral disease","umls","C0041954"
> "1426","ureteral disease","mondo","0001926"
5620,5626c9341,9347
< "12328","marasmus","icd10cm","E41"
< "12328","marasmus","icd9cm","261"
< "12328","marasmus","mesh","D011502"
< "12328","marasmus","umls","C0086588"
< "12328","marasmus","mondo","0006848"
< "5438","extrahepatic bile duct adenoma","umls","C1331534"
< "5438","extrahepatic bile duct adenoma","mondo","0003445"
---
> "9192","dyskinesia of esophagus","icd10cm","K22.4"
> "9192","dyskinesia of esophagus","icd9cm","530.5"
> "9192","dyskinesia of esophagus","mesh","D015154"
> "9192","dyskinesia of esophagus","umls","C0014858"
> "9192","dyskinesia of esophagus","mondo","0004729"
> "7941","Barrett's adenocarcinoma","umls","C1332460"
> "7941","Barrett's adenocarcinoma","mondo","0004405"
5629,5633c9350,9359
< "14221","abdominal obesity-metabolic syndrome 1","icd10cm","E88.81"
< "14221","abdominal obesity-metabolic syndrome 1","icd9cm","277.7"
< "14221","abdominal obesity-metabolic syndrome 1","mesh","D024821"
< "14221","abdominal obesity-metabolic syndrome 1","umls","C0524620"
< "14221","abdominal obesity-metabolic syndrome 1","mondo","0011565"
---
> "0110259","cataract 43","icd10cm","Q12.0"
> "0110259","cataract 43","mondo","0014565"
> "3367","bone leiomyosarcoma","umls","C1332579"
> "3367","bone leiomyosarcoma","mondo","0002624"
> "14224","tracheal calcification","umls","C0264324"
> "14224","tracheal calcification","mondo","0001911"
> "10378","disuse amblyopia","icd10cm","H53.01"
> "10378","disuse amblyopia","icd9cm","368.02"
> "10378","disuse amblyopia","umls","C0152189"
> "10378","disuse amblyopia","mondo","0001022"
5656,5679c9382,9387
< "0050710","3-Methylcrotonyl-CoA carboxylase deficiency","mondo","0018950"
< "0070137","autosomal recessive cutis laxa type IIB","icd10cm","Q82.8"
< "0070137","autosomal recessive cutis laxa type IIB","mondo","0013051"
< "9036","parotid gland cancer","icd10cm","C07"
< "9036","parotid gland cancer","icd9cm","142.0"
< "9036","parotid gland cancer","mesh","D010307"
< "9036","parotid gland cancer","umls","C0747273"
< "9036","parotid gland cancer","mondo","0004700"
< "7016","tendon sheath lipoma","umls","C1336703"
< "7016","tendon sheath lipoma","mondo","0004076"
< "10250","louping ill","icd10cm","A84.8"
< "10250","louping ill","icd9cm","063.1"
< "10250","louping ill","mesh","D008146"
< "10250","louping ill","umls","C0024025"
< "10250","louping ill","mondo","0005829"
< "0110879","holoprosencephaly 8","mondo","0012267"
< "1738","small intestine leiomyoma","umls","C0238197"
< "1738","small intestine leiomyoma","mondo","0002092"
< "1733","cryptosporidiosis","icd10cm","A07.2"
< "1733","cryptosporidiosis","icd9cm","007.4"
< "1733","cryptosporidiosis","mesh","D003457"
< "1733","cryptosporidiosis","umls","C0010418"
< "1733","cryptosporidiosis","mondo","0015474"
< "0040057","benzoic acid allergic contact dermatitis","umls","C0571102"
---
> "0050640","anauxetic dysplasia 1","mondo","0011773"
> "0050641","Rh deficiency syndrome","mondo","0019107"
> "0050644","arterial calcification of infancy","mesh","C537440"
> "0050644","arterial calcification of infancy","mondo","0018870"
> "0050645","arterial tortuosity syndrome","mesh","C565942"
> "0050645","arterial tortuosity syndrome","mondo","0008818"
5682,5757c9390,9395
< "11887","ureter leiomyoma","umls","C1336875"
< "11887","ureter leiomyoma","mondo","0001399"
< "5041","esophageal cancer","icd10cm","C15.3"
< "5041","esophageal cancer","icd10cm","C15.4"
< "5041","esophageal cancer","icd10cm","C15.5"
< "5041","esophageal cancer","icd9cm","150.2"
< "5041","esophageal cancer","icd9cm","150.3"
< "5041","esophageal cancer","icd9cm","150.4"
< "5041","esophageal cancer","icd9cm","150.5"
< "5041","esophageal cancer","icd9cm","150.8"
< "5041","esophageal cancer","mesh","D004938"
< "5041","esophageal cancer","umls","C0014859"
< "5041","esophageal cancer","umls","C0153413"
< "5041","esophageal cancer","umls","C0153414"
< "5041","esophageal cancer","umls","C0153415"
< "5041","esophageal cancer","umls","C0153416"
< "5041","esophageal cancer","umls","C0496775"
< "5041","esophageal cancer","mondo","0007576"
< "11812","bladder sarcoma","umls","C0349666"
< "11812","bladder sarcoma","mondo","0001374"
< "0110416","retinitis pigmentosa 24","icd10cm","H35.5"
< "0110416","retinitis pigmentosa 24","mondo","0010259"
< "0110417","retinitis pigmentosa 34","icd10cm","H35.5"
< "0110417","retinitis pigmentosa 34","mondo","0010374"
< "0110414","retinitis pigmentosa 3","icd10cm","H35.5"
< "0110414","retinitis pigmentosa 3","mondo","0010227"
< "10371","yaws","icd10cm","A66"
< "10371","yaws","icd10cm","A66.9"
< "10371","yaws","icd9cm","102"
< "10371","yaws","icd9cm","102.9"
< "10371","yaws","mesh","D015001"
< "10371","yaws","umls","C0043388"
< "10371","yaws","mondo","0006019"
< "0110412","retinitis pigmentosa 23","icd10cm","H35.5"
< "0110412","retinitis pigmentosa 23","mondo","0010320"
< "11819","ureter cancer","icd10cm","C66"
< "11819","ureter cancer","icd9cm","189.2"
< "11819","ureter cancer","mesh","D014516"
< "11819","ureter cancer","umls","C0153619"
< "11819","ureter cancer","mondo","0008627"
< "0110410","retinitis pigmentosa 69","icd10cm","H35.5"
< "0110410","retinitis pigmentosa 69","mondo","0014345"
< "13129","severe pre-eclampsia","icd9cm","642.50"
< "13129","severe pre-eclampsia","umls","C0156669"
< "13129","severe pre-eclampsia","mondo","0001641"
< "0050999","autosomal recessive spinocerebellar ataxia 10","mondo","0013392"
< "754","bladder tuberculosis","icd10cm","A18.12"
< "754","bladder tuberculosis","icd9cm","016.1"
< "754","bladder tuberculosis","icd9cm","016.10"
< "754","bladder tuberculosis","umls","C0152793"
< "754","bladder tuberculosis","mondo","0004272"
< "0110674","congenital myasthenic syndrome 17","mondo","0014578"
< "57","aortic valve insufficiency","icd10cm","I06.1"
< "57","aortic valve insufficiency","icd9cm","395.1"
< "57","aortic valve insufficiency","icd9cm","396.3"
< "57","aortic valve insufficiency","mesh","D001022"
< "57","aortic valve insufficiency","umls","C0003504"
< "57","aortic valve insufficiency","umls","C0155568"
< "57","aortic valve insufficiency","umls","C0264774"
< "57","aortic valve insufficiency","mondo","0005648"
< "1595","endogenous depression","mesh","D003866"
< "1595","endogenous depression","umls","C0011573"
< "1595","endogenous depression","umls","C0041696"
< "1595","endogenous depression","mondo","0012048"
< "0070098","oculocutaneous albinism type IV","mondo","0011683"
< "3074","giant cell glioblastoma","mesh","D005909"
< "3074","giant cell glioblastoma","umls","C0334588"
< "3074","giant cell glioblastoma","mondo","0016682"
< "0060185","Clostridium difficile colitis","icd10cm","A04.7"
< "0060185","Clostridium difficile colitis","mesh","D004761"
< "0060185","Clostridium difficile colitis","umls","C0014358"
< "0060185","Clostridium difficile colitis","umls","C0085819"
< "0060185","Clostridium difficile colitis","umls","C1257843"
< "0060185","Clostridium difficile colitis","umls","C1257844"
< "0060185","Clostridium difficile colitis","umls","C1257845"
< "0060185","Clostridium difficile colitis","mondo","0000705"
---
> "0050646","distal arthrogryposis","mondo","0019942"
> "0050647","Arts syndrome","mesh","C535388"
> "0050647","Arts syndrome","umls","C0796028"
> "0050647","Arts syndrome","mondo","0010533"
> "6886","ureter small cell carcinoma","umls","C1336878"
> "6886","ureter small cell carcinoma","mondo","0006482"
5760,5812c9398,9411
< "3078","grade III astrocytoma","mesh","D001254"
< "3078","grade III astrocytoma","umls","C0334579"
< "3078","grade III astrocytoma","mondo","0016684"
< "0060189","ileitis","icd10cm","K52.9"
< "0060189","ileitis","mesh","D007079"
< "0060189","ileitis","umls","C0020877"
< "0060189","ileitis","mondo","0000709"
< "0060210","amyotrophic lateral sclerosis type 19","mondo","0014223"
< "0060211","amyotrophic lateral sclerosis type 20","mondo","0014181"
< "0060212","amyotrophic lateral sclerosis type 21","mondo","0011632"
< "0060213","FTDALS1","mondo","0007105"
< "0060214","FTDALS2","mondo","0014395"
< "0060215","Balo concentric sclerosis","icd10cm","G31.81"
< "0060215","Balo concentric sclerosis","icd10cm","G37.0"
< "0060215","Balo concentric sclerosis","icd9cm","341.1"
< "0060215","Balo concentric sclerosis","mesh","D002549"
< "0060215","Balo concentric sclerosis","umls","C0004712"
< "0060215","Balo concentric sclerosis","umls","C0007795"
< "0060215","Balo concentric sclerosis","umls","C0205710"
< "0060215","Balo concentric sclerosis","mondo","0016430"
< "1023","borderline leprosy","icd10cm","A30.3"
< "1023","borderline leprosy","icd9cm","030.3"
< "1023","borderline leprosy","mesh","D015439"
< "1023","borderline leprosy","umls","C0023346"
< "1023","borderline leprosy","mondo","0005125"
< "0050866","oral squamous cell carcinoma","mondo","0004958"
< "5348","adult endodermal sinus tumor","umls","C1332221"
< "5348","adult endodermal sinus tumor","mondo","0003404"
< "936","brain disease","icd10cm","G93.40"
< "936","brain disease","icd10cm","G93.9"
< "936","brain disease","icd9cm","348.3"
< "936","brain disease","icd9cm","348.30"
< "936","brain disease","icd9cm","348.9"
< "936","brain disease","mesh","D001927"
< "936","brain disease","umls","C0006111"
< "936","brain disease","umls","C0085584"
< "936","brain disease","mondo","0005560"
< "3981","pantothenate kinase-associated neurodegeneration","icd10cm","G23.0"
< "3981","pantothenate kinase-associated neurodegeneration","mesh","D006211"
< "3981","pantothenate kinase-associated neurodegeneration","umls","C0018523"
< "3981","pantothenate kinase-associated neurodegeneration","mondo","0009319"
< "0111122","nephronophthisis 14","mondo","0013916"
< "4364","malignant breast melanoma","umls","C0346787"
< "4364","malignant breast melanoma","mondo","0002975"
< "4367","apparent mineralocorticoid excess syndrome","mesh","D043204"
< "4367","apparent mineralocorticoid excess syndrome","umls","C0342488"
< "4367","apparent mineralocorticoid excess syndrome","mondo","0006657"
< "8991","cervix uteri carcinoma in situ","icd10cm","D06"
< "8991","cervix uteri carcinoma in situ","icd10cm","D06.9"
< "8991","cervix uteri carcinoma in situ","icd9cm","233.1"
< "8991","cervix uteri carcinoma in situ","mesh","D018290"
< "8991","cervix uteri carcinoma in situ","umls","C0851140"
< "8991","cervix uteri carcinoma in situ","mondo","0042487"
---
> "6888","ureter transitional cell carcinoma","umls","C0577692"
> "6888","ureter transitional cell carcinoma","mondo","0004030"
> "605","flying phobia","umls","C0344318"
> "605","flying phobia","mondo","0003748"
> "607","paraplegia","icd10cm","G82.2"
> "607","paraplegia","icd10cm","G82.20"
> "607","paraplegia","icd9cm","344.1"
> "607","paraplegia","mesh","D010264"
> "607","paraplegia","umls","C0030486"
> "607","paraplegia","mondo","0003757"
> "606","Brown-Sequard syndrome","icd10cm","G83.81"
> "606","Brown-Sequard syndrome","mesh","D018437"
> "606","Brown-Sequard syndrome","umls","C0242644"
> "606","Brown-Sequard syndrome","mondo","0003754"
5819,5826c9418,9421
< "4362","cervical cancer","icd10cm","C53"
< "4362","cervical cancer","icd10cm","C53.9"
< "4362","cervical cancer","icd9cm","180"
< "4362","cervical cancer","icd9cm","180.9"
< "4362","cervical cancer","mesh","D002583"
< "4362","cervical cancer","umls","C0007847"
< "4362","cervical cancer","umls","C0007873"
< "4362","cervical cancer","mondo","0002974"
---
> "603","AIDS phobia","umls","C0853870"
> "603","AIDS phobia","mondo","0003740"
> "602","cancerophobia","umls","C0233705"
> "602","cancerophobia","mondo","0003736"
5831,5837d9425
< "12894","Sjogren's syndrome","icd10cm","M35.0"
< "12894","Sjogren's syndrome","icd10cm","M35.00"
< "12894","Sjogren's syndrome","icd9cm","710.2"
< "12894","Sjogren's syndrome","mesh","D012859"
< "12894","Sjogren's syndrome","umls","C0086981"
< "12894","Sjogren's syndrome","umls","C1527336"
< "12894","Sjogren's syndrome","mondo","0010030"
5842,5843c9430,9439
< "0060586","Noonan syndrome 8","icd10cm","Q87.1"
< "0060586","Noonan syndrome 8","mondo","0014143"
---
> "1201","trigeminal nerve neoplasm","umls","C1263897"
> "1201","trigeminal nerve neoplasm","mondo","0001420"
> "4271","microsporidiosis","icd10cm","B60.8"
> "4271","microsporidiosis","mesh","D016881"
> "4271","microsporidiosis","umls","C0085407"
> "4271","microsporidiosis","mondo","0005846"
> "1203","drug-induced mental disorder","icd9cm","292.8"
> "1203","drug-induced mental disorder","icd9cm","292.89"
> "1203","drug-induced mental disorder","umls","C0154325"
> "1203","drug-induced mental disorder","mondo","0001423"
5846,5852c9442,9449
< "4270","encephalitozoonosis","mesh","D016890"
< "4270","encephalitozoonosis","umls","C0085412"
< "4270","encephalitozoonosis","mondo","0005743"
< "0110678","congenital myasthenic syndrome 4A","mondo","0011600"
< "6041","choroid spindle cell melanoma","umls","C1333027"
< "6041","choroid spindle cell melanoma","mondo","0003745"
< "0110679","congenital myasthenic syndrome 4C","mondo","0012157"
---
> "0060587","Noonan syndrome 9","icd10cm","Q87.1"
> "0060587","Noonan syndrome 9","mondo","0014691"
> "4277","penis basal cell carcinoma","umls","C1518949"
> "4277","penis basal cell carcinoma","mondo","0002935"
> "8275","intratubular embryonal carcinoma","umls","C1336096"
> "8275","intratubular embryonal carcinoma","mondo","0004520"
> "8274","synovial angioma","umls","C1336546"
> "8274","synovial angioma","mondo","0004519"
5855,5918c9452,9463
< "11079","leech infestation","icd10cm","B88.3"
< "11079","leech infestation","icd9cm","134.2"
< "11079","leech infestation","umls","C0019575"
< "11079","leech infestation","mondo","0001191"
< "4997","Camurati-Engelmann disease","icd10cm","Q78.3"
< "4997","Camurati-Engelmann disease","mesh","C538411"
< "4997","Camurati-Engelmann disease","mesh","D003966"
< "4997","Camurati-Engelmann disease","umls","C0011989"
< "4997","Camurati-Engelmann disease","mondo","0007542"
< "11077","brucellosis","icd10cm","A23"
< "11077","brucellosis","icd10cm","A23.9"
< "11077","brucellosis","icd9cm","023"
< "11077","brucellosis","icd9cm","023.9"
< "11077","brucellosis","mesh","D002006"
< "11077","brucellosis","umls","C0006309"
< "11077","brucellosis","mondo","0005683"
< "3103","thoracic outlet syndrome","icd10cm","G54.0"
< "3103","thoracic outlet syndrome","mesh","D013901"
< "3103","thoracic outlet syndrome","umls","C0039984"
< "3103","thoracic outlet syndrome","mondo","0005979"
< "1561","cognitive disorder","icd10cm","F09"
< "1561","cognitive disorder","mesh","D019965"
< "1561","cognitive disorder","umls","C0029227"
< "1561","cognitive disorder","mondo","0002039"
< "1443","cerebral degeneration","icd9cm","331.9"
< "1443","cerebral degeneration","umls","C0154671"
< "1443","cerebral degeneration","mondo","0022687"
< "1442","Alpers syndrome","icd10cm","G31.81"
< "1442","Alpers syndrome","mesh","D002549"
< "1442","Alpers syndrome","umls","C0205710"
< "1442","Alpers syndrome","mondo","0008758"
< "1441","autosomal dominant cerebellar ataxia","mesh","D020754"
< "1441","autosomal dominant cerebellar ataxia","umls","C0087012"
< "1441","autosomal dominant cerebellar ataxia","mondo","0020380"
< "1440","Machado-Joseph disease","mesh","D017827"
< "1440","Machado-Joseph disease","umls","C0024408"
< "1440","Machado-Joseph disease","mondo","0007182"
< "3707","endometrial mucinous adenocarcinoma","umls","C1519859"
< "3707","endometrial mucinous adenocarcinoma","mondo","0002747"
< "0050997","cerebellar ataxia, mental retardation and dysequlibrium syndrome","mondo","0009133"
< "0110948","Waardenburg syndrome type 1","mesh","D014849"
< "0110948","Waardenburg syndrome type 1","umls","C1847800"
< "0110948","Waardenburg syndrome type 1","mondo","0008670"
< "4090","agnosia","icd10cm","R48.1"
< "4090","agnosia","icd10cm","R48.2"
< "4090","agnosia","mesh","D000377"
< "4090","agnosia","mesh","D001072"
< "4090","agnosia","umls","C0001816"
< "4090","agnosia","umls","C0003635"
< "4090","agnosia","mondo","0005638"
< "0060720","autosomal recessive congenital ichthyosis 11","icd10cm","Q80.8"
< "0060720","autosomal recessive congenital ichthyosis 11","mondo","0011218"
< "4990","essential tremor","icd10cm","G25.0"
< "4990","essential tremor","mesh","D020329"
< "4990","essential tremor","umls","C0270736"
< "4990","essential tremor","mondo","0003233"
< "00600891","juvenile onset Parkinson's disease 19A","icd10cm","G20"
< "9699","ophthalmia neonatorum","icd10cm","P39.1"
< "9699","ophthalmia neonatorum","icd9cm","771.6"
< "9699","ophthalmia neonatorum","umls","C0027611"
< "9699","ophthalmia neonatorum","umls","C0029076"
< "9699","ophthalmia neonatorum","mondo","0004854"
< "0060728","NGLY1-deficiency","icd10cm","E77.8"
< "0060728","NGLY1-deficiency","mondo","0014109"
---
> "13964","Morgagni cataract","icd9cm","366.18"
> "13964","Morgagni cataract","umls","C0152258"
> "13964","Morgagni cataract","mondo","0001848"
> "461","muscle benign neoplasm","mesh","D009379"
> "461","muscle benign neoplasm","mesh","D019042"
> "461","muscle benign neoplasm","umls","C0027664"
> "461","muscle benign neoplasm","umls","C0282606"
> "461","muscle benign neoplasm","mondo","0003061"
> "8419","colloid adenoma","umls","C0334329"
> "8419","colloid adenoma","mondo","0004558"
> "8418","congenital fibrosarcoma","umls","C0334459"
> "8418","congenital fibrosarcoma","mondo","0004557"
5924,5925c9469,9484
< "0110775","hereditary spastic paraplegia 24","icd10cm","G11.4"
< "0110775","hereditary spastic paraplegia 24","mondo","0011862"
---
> "8411","kidney angiomyolipoma","umls","C0241961"
> "8411","kidney angiomyolipoma","mondo","0004555"
> "8410","childhood kidney angiomyolipoma","umls","C1333000"
> "8410","childhood kidney angiomyolipoma","mondo","0004554"
> "0111372","autosomal dominant endosteal hyperostosis","mesh","C536748"
> "0111372","autosomal dominant endosteal hyperostosis","umls","C0432273"
> "8415","carcinoma arising in nasal papillomatosis","umls","C1332840"
> "8415","carcinoma arising in nasal papillomatosis","mondo","0004556"
> "0111373","familial progressive hyperpigmentation with or without hypopigmentation","umls","CN030522"
> "9809","hypersensitivity vasculitis","icd10cm","D69.0"
> "9809","hypersensitivity vasculitis","icd10cm","M31.0"
> "9809","hypersensitivity vasculitis","icd9cm","446.2"
> "9809","hypersensitivity vasculitis","icd9cm","446.20"
> "9809","hypersensitivity vasculitis","mesh","D018366"
> "9809","hypersensitivity vasculitis","umls","C0151436"
> "9809","hypersensitivity vasculitis","mondo","0006794"
5931,5962c9490,9507
< "6460","large intestine lipoma","umls","C1333114"
< "6460","large intestine lipoma","mondo","0003885"
< "6231","mature teratoma of the ovary","umls","C1334637"
< "6231","mature teratoma of the ovary","mondo","0003820"
< "0070099","oculocutaneous albinism type V","mondo","0014127"
< "0110826","Usher syndrome type 1","icd10cm","H35.5"
< "0110826","Usher syndrome type 1","umls","C0339533"
< "0110826","Usher syndrome type 1","mondo","0010168"
< "6230","childhood teratoma of the ovary","umls","C1332992"
< "6230","childhood teratoma of the ovary","mondo","0003819"
< "4998","trichorhinophalangeal syndrome type II","mesh","D015826"
< "4998","trichorhinophalangeal syndrome type II","umls","C0023003"
< "4998","trichorhinophalangeal syndrome type II","mondo","0007874"
< "4724","brain edema","mesh","D001929"
< "4724","brain edema","umls","C1527311"
< "4724","brain edema","mondo","0006684"
< "0110770","hereditary spastic paraplegia 17","icd10cm","G11.4"
< "0110770","hereditary spastic paraplegia 17","mondo","0010043"
< "2303","stereotypic movement disorder","icd10cm","F98.4"
< "2303","stereotypic movement disorder","icd9cm","307.3"
< "2303","stereotypic movement disorder","mesh","D019956"
< "2303","stereotypic movement disorder","umls","C0038273"
< "2303","stereotypic movement disorder","mondo","0002265"
< "7725","epilepsy with generalized tonic-clonic seizures","mesh","D004830"
< "7725","epilepsy with generalized tonic-clonic seizures","umls","C0014549"
< "7725","epilepsy with generalized tonic-clonic seizures","mondo","0005754"
< "248","trachea leiomyoma","mesh","D014134"
< "248","trachea leiomyoma","umls","C0040582"
< "248","trachea leiomyoma","umls","C1336772"
< "248","trachea leiomyoma","mondo","0002318"
< "4049","mediastinum rhabdomyosarcoma","umls","C1334677"
< "4049","mediastinum rhabdomyosarcoma","mondo","0002851"
---
> "7584","subglottis verrucous carcinoma","umls","C0280330"
> "7584","subglottis verrucous carcinoma","mondo","0004290"
> "7585","subglottis squamous cell carcinoma","umls","C0280326"
> "7585","subglottis squamous cell carcinoma","mondo","0004291"
> "7586","supraglottis verrucous carcinoma","umls","C0280331"
> "7586","supraglottis verrucous carcinoma","mondo","0004292"
> "7587","supraglottis squamous cell carcinoma","umls","C0749163"
> "7587","supraglottis squamous cell carcinoma","mondo","0004293"
> "2058","chronic mucocutaneous candidiasis","mesh","D002178"
> "2058","chronic mucocutaneous candidiasis","umls","C0006845"
> "2058","chronic mucocutaneous candidiasis","mondo","0015279"
> "9801","tuberculous peritonitis","icd10cm","A18.31"
> "9801","tuberculous peritonitis","icd9cm","014.0"
> "9801","tuberculous peritonitis","mesh","D014395"
> "9801","tuberculous peritonitis","umls","C0041325"
> "9801","tuberculous peritonitis","mondo","0006000"
> "7583","glottis verrucous carcinoma","umls","C0280329"
> "7583","glottis verrucous carcinoma","mondo","0004289"
5965a9511,15821
> "6483","rete testis adenoma","umls","C1514910"
> "6483","rete testis adenoma","mondo","0003893"
> "4148","gastrointestinal neuroendocrine benign tumor","umls","C1333799"
> "4148","gastrointestinal neuroendocrine benign tumor","mondo","0002891"
> "4147","gastrointestinal adenoma","umls","C0948101"
> "4147","gastrointestinal adenoma","mondo","0006180"
> "4141","intraorbital meningioma","mesh","D008579"
> "4141","intraorbital meningioma","umls","C1334261"
> "4141","intraorbital meningioma","mondo","0002888"
> "4140","biliary dyskinesia","mesh","D001657"
> "4140","biliary dyskinesia","umls","C0005416"
> "4140","biliary dyskinesia","mondo","0005667"
> "4143","orbital cancer","icd10cm","C69.6"
> "4143","orbital cancer","icd9cm","190.1"
> "4143","orbital cancer","mesh","D009918"
> "4143","orbital cancer","umls","C0029185"
> "4143","orbital cancer","umls","C0153626"
> "4143","orbital cancer","mondo","0002889"
> "3856","male reproductive organ cancer","icd10cm","C60-C63"
> "3856","male reproductive organ cancer","icd10cm","C63.9"
> "3856","male reproductive organ cancer","icd9cm","187.9"
> "3856","male reproductive organ cancer","mesh","D005834"
> "3856","male reproductive organ cancer","umls","C0017417"
> "3856","male reproductive organ cancer","umls","C0153606"
> "3856","male reproductive organ cancer","mondo","0005836"
> "3857","large cell medulloblastoma","umls","C1266180"
> "3857","large cell medulloblastoma","mondo","0002791"
> "3855","seminal vesicle tumor","umls","C0341767"
> "3855","seminal vesicle tumor","mondo","0002790"
> "3852","Peutz-Jeghers syndrome","icd10cm","Q85.8"
> "3852","Peutz-Jeghers syndrome","mesh","D010580"
> "3852","Peutz-Jeghers syndrome","umls","C0031269"
> "3852","Peutz-Jeghers syndrome","umls","C0265323"
> "3852","Peutz-Jeghers syndrome","umls","C0456487"
> "3852","Peutz-Jeghers syndrome","mondo","0008280"
> "3850","hemangiopericytic tumor","umls","C0476144"
> "3850","hemangiopericytic tumor","mondo","0002789"
> "992","Omsk hemorrhagic fever","icd10cm","A98.1"
> "992","Omsk hemorrhagic fever","icd9cm","065.1"
> "992","Omsk hemorrhagic fever","mesh","D006481"
> "992","Omsk hemorrhagic fever","umls","C0019103"
> "992","Omsk hemorrhagic fever","mondo","0017882"
> "0080160","Cytomegalovirus retinitis","mesh","D017726"
> "0080160","Cytomegalovirus retinitis","mondo","0000878"
> "0080161","cutaneous candidiasis","mesh","D002179"
> "0080161","cutaneous candidiasis","mondo","0000879"
> "0080162","lupus nephritis","mesh","D008181"
> "0080162","lupus nephritis","mondo","0005556"
> "0080163","otulipenia","mondo","0014912"
> "0080164","myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1","umls","C2827356"
> "0080164","myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1","mondo","0000881"
> "0080165","myeloid and lymphoid neoplasms associated with PDGFRA rearrangement","mondo","0000882"
> "0080166","myeloid neoplasms associated with PDGFRB rearrangement","mondo","0000883"
> "0080167","myeloid and lymphoid neoplasms associated with FGFR1 abnormalities","mondo","0000884"
> "0080169","tricuspid atresia","mesh","D018785"
> "0080169","tricuspid atresia","mondo","0011514"
> "14671","multiple intestinal atresia","mesh","C562441"
> "14671","multiple intestinal atresia","umls","C0220744"
> "14671","multiple intestinal atresia","mondo","0009465"
> "5914","nonencapsulated sclerosing carcinoma","umls","C0334330"
> "5914","nonencapsulated sclerosing carcinoma","mondo","0003701"
> "5916","uterine corpus leiomyomatosis","umls","C1519855"
> "5916","uterine corpus leiomyomatosis","mondo","0003703"
> "5913","brachial plexus neoplasm","umls","C1332602"
> "5913","brachial plexus neoplasm","mondo","0003700"
> "4558","Ludwig's angina","mesh","D008158"
> "4558","Ludwig's angina","umls","C0024081"
> "4558","Ludwig's angina","mondo","0006576"
> "4556","lung large cell carcinoma","umls","C0345958"
> "4556","lung large cell carcinoma","mondo","0003050"
> "4557","oral leukoedema","mesh","D007967"
> "4557","oral leukoedema","umls","C0023523"
> "4557","oral leukoedema","mondo","0006880"
> "4554","type C thymoma","umls","C1322286"
> "4554","type C thymoma","mondo","0006451"
> "4555","ovarian large-cell neuroendocrine carcinoma","umls","C1335174"
> "4555","ovarian large-cell neuroendocrine carcinoma","mondo","0003049"
> "4552","large cell carcinoma","mesh","D018287"
> "4552","large cell carcinoma","umls","C0206704"
> "4552","large cell carcinoma","mondo","0005232"
> "4553","thymus large cell carcinoma","umls","C1334364"
> "4553","thymus large cell carcinoma","mondo","0003047"
> "4550","anal gland neoplasm","mesh","D000694"
> "4550","anal gland neoplasm","umls","C0002757"
> "4550","anal gland neoplasm","mondo","0003045"
> "4551","anus benign neoplasm","mesh","D001005"
> "4551","anus benign neoplasm","umls","C0003463"
> "4551","anus benign neoplasm","mondo","0003046"
> "0090008","immunodeficiency-centromeric instability-facial anomalies syndrome 1","icd10cm","D84.8"
> "0090008","immunodeficiency-centromeric instability-facial anomalies syndrome 1","mondo","0009454"
> "0090009","immunodeficiency-centromeric instability-facial anomalies syndrome 2","icd10cm","D84.8"
> "0090009","immunodeficiency-centromeric instability-facial anomalies syndrome 2","mondo","0013553"
> "0090006","renal coloboma syndrome","icd10cm","Q60.4"
> "0090006","renal coloboma syndrome","mondo","0007352"
> "0090007","immunodeficiency-centromeric instability-facial anomalies syndrome","icd10cm","D84.8"
> "0090007","immunodeficiency-centromeric instability-facial anomalies syndrome","mondo","0000133"
> "0090004","progressive pseudorheumatoid arthropathy of childhood","icd10cm","Q77.7"
> "0090004","progressive pseudorheumatoid arthropathy of childhood","mondo","0008827"
> "0090005","Schwartz-Jampel syndrome 1","icd10cm","G71.1"
> "0090005","Schwartz-Jampel syndrome 1","mondo","0009717"
> "0090002","Tietz syndrome","mondo","0007077"
> "0090003","agenesis of the corpus callosum with peripheral neuropathy","icd10cm","G60.0"
> "0090003","agenesis of the corpus callosum with peripheral neuropathy","mondo","0000902"
> "0090001","Fraser syndrome","icd10cm","Q87.0"
> "0090001","Fraser syndrome","mesh","D058497"
> "0090001","Fraser syndrome","mondo","0009046"
> "0050266","tungiasis","mesh","D058285"
> "0050266","tungiasis","mondo","0019498"
> "0050269","Trichomonas vaginalis trichomoniasis","icd10cm","A59.00"
> "0050269","Trichomonas vaginalis trichomoniasis","mesh","D014247"
> "0050269","Trichomonas vaginalis trichomoniasis","mondo","0005993"
> "14497","Wolman disease","icd10cm","E75.5"
> "14497","Wolman disease","mesh","D015223"
> "14497","Wolman disease","umls","C0043208"
> "14497","Wolman disease","mondo","0019148"
> "0110733","neuronal ceroid lipofuscinosis 9","icd10cm","E75.4"
> "0110733","neuronal ceroid lipofuscinosis 9","mondo","0012188"
> "0110732","neuronal ceroid lipofuscinosis 11","icd10cm","E75.4"
> "0110732","neuronal ceroid lipofuscinosis 11","mondo","0013866"
> "0110731","neuronal ceroid lipofuscinosis 3","icd10cm","E75.4"
> "0110731","neuronal ceroid lipofuscinosis 3","mondo","0008767"
> "0110730","neuronal ceroid lipofuscinosis 4A","icd10cm","E75.4"
> "0110730","neuronal ceroid lipofuscinosis 4A","mondo","0008768"
> "0110737","neurodegeneration with brain iron accumulation 3","mesh","C548080"
> "0110737","neurodegeneration with brain iron accumulation 3","umls","C1853578"
> "0110737","neurodegeneration with brain iron accumulation 3","mondo","0011638"
> "0110736","neurodegeneration with brain iron accumulation 2b","icd10cm","G23.0"
> "0110736","neurodegeneration with brain iron accumulation 2b","mondo","0012444"
> "0110735","neurodegeneration with brain iron accumulation 2a","icd10cm","G23.0"
> "0110735","neurodegeneration with brain iron accumulation 2a","mondo","0024457"
> "0110734","neurodegeneration with brain iron accumulation","mesh","C538421"
> "0110734","neurodegeneration with brain iron accumulation","umls","C2931845"
> "0110734","neurodegeneration with brain iron accumulation","mondo","0018307"
> "0110739","neurodegeneration with brain iron accumulation 5","icd10cm","G23.0"
> "0110739","neurodegeneration with brain iron accumulation 5","mondo","0010476"
> "0110738","neurodegeneration with brain iron accumulation 4","icd10cm","G23.0"
> "0110738","neurodegeneration with brain iron accumulation 4","mondo","0013674"
> "0110889","inflammatory bowel disease 5","mondo","0011661"
> "0110888","inflammatory bowel disease 18","mondo","0012841"
> "12087","deep corneal vascularisation","icd10cm","H16.44"
> "12087","deep corneal vascularisation","icd9cm","370.63"
> "12087","deep corneal vascularisation","umls","C0155095"
> "12087","deep corneal vascularisation","mondo","0001430"
> "12084","transient arthropathy","icd9cm","716.41"
> "12084","transient arthropathy","umls","C0158007"
> "12084","transient arthropathy","mondo","0001429"
> "2616","Wolffian duct adenoma","umls","C0334530"
> "2616","Wolffian duct adenoma","mondo","0002364"
> "2615","papilloma","mesh","D010212"
> "2615","papilloma","umls","C0030354"
> "2615","papilloma","umls","C0205875"
> "2615","papilloma","mondo","0002363"
> "2614","serous surface papilloma","umls","C0334360"
> "2614","serous surface papilloma","mondo","0002362"
> "0070202","familial partial lipodystrophy type 2","umls","C1720860"
> "0070202","familial partial lipodystrophy type 2","mondo","0007906"
> "0070203","familial partial lipodystrophy type 5","mondo","0014098"
> "0070200","Miyoshi muscular dystrophy 2","mondo","0013221"
> "0070201","Miyoshi muscular dystrophy 3","umls","C2750076"
> "0070201","Miyoshi muscular dystrophy 3","mondo","0013222"
> "0070206","familial partial lipodystrophy type 6","mondo","0014431"
> "0070207","familial partial lipodystrophy type 1","umls","C1720859"
> "0070207","familial partial lipodystrophy type 1","mondo","0012072"
> "7340","pediatric ovarian dysgerminoma","umls","C1332988"
> "7340","pediatric ovarian dysgerminoma","mondo","0004193"
> "0070205","familial partial lipodystrophy type 4","mondo","0013478"
> "10794","sphenoid sinusitis","icd10cm","J32.3"
> "10794","sphenoid sinusitis","mesh","D015524"
> "10794","sphenoid sinusitis","umls","C0037886"
> "10794","sphenoid sinusitis","mondo","0005964"
> "10027","tabes dorsalis","icd10cm","A52.11"
> "10027","tabes dorsalis","icd9cm","094.0"
> "10027","tabes dorsalis","mesh","D013606"
> "10027","tabes dorsalis","umls","C0039223"
> "10027","tabes dorsalis","mondo","0005977"
> "0070208","hereditary lymphedema IC","mondo","0013278"
> "0070209","hereditary lymphedema ID","mondo","0014393"
> "10022","ampulla of Vater neoplasm","umls","C0345916"
> "10022","ampulla of Vater neoplasm","mondo","0000921"
> "10791","frontal sinusitis","icd10cm","J32.1"
> "10791","frontal sinusitis","mesh","D015522"
> "10791","frontal sinusitis","umls","C0016735"
> "10791","frontal sinusitis","mondo","0001121"
> "10020","ampulla of Vater cancer","icd10cm","C24.1"
> "10020","ampulla of Vater cancer","icd9cm","156.2"
> "10020","ampulla of Vater cancer","umls","C0153454"
> "10020","ampulla of Vater cancer","mondo","0000919"
> "10021","duodenum cancer","icd10cm","C17.0"
> "10021","duodenum cancer","icd9cm","152.0"
> "10021","duodenum cancer","mesh","D004379"
> "10021","duodenum cancer","umls","C0153426"
> "10021","duodenum cancer","umls","C0541912"
> "10021","duodenum cancer","mondo","0000920"
> "0110089","asphyxiating thoracic dystrophy 5","icd10cm","Q77.2"
> "0110089","asphyxiating thoracic dystrophy 5","mondo","0013717"
> "0110088","asphyxiating thoracic dystrophy 4","icd10cm","Q77.2"
> "0110088","asphyxiating thoracic dystrophy 4","mondo","0013441"
> "0110085","asphyxiating thoracic dystrophy 1","icd10cm","Q77.2"
> "0110085","asphyxiating thoracic dystrophy 1","mondo","0008831"
> "0110084","arrhythmogenic right ventricular dysplasia 13","icd10cm","I42.8"
> "0110084","arrhythmogenic right ventricular dysplasia 13","mondo","0000908"
> "0110087","asphyxiating thoracic dystrophy 3","icd10cm","Q77.2"
> "0110087","asphyxiating thoracic dystrophy 3","mondo","0013127"
> "0110086","asphyxiating thoracic dystrophy 2","icd10cm","Q77.2"
> "0110086","asphyxiating thoracic dystrophy 2","mondo","0012644"
> "0110081","arrhythmogenic right ventricular dysplasia 10","icd10cm","I42.8"
> "0110081","arrhythmogenic right ventricular dysplasia 10","mondo","0012434"
> "0110080","Leber congenital amaurosis 12","icd10cm","H35.5"
> "0110080","Leber congenital amaurosis 12","mondo","0012525"
> "0110083","arrhythmogenic right ventricular dysplasia 12","icd10cm","I42.8"
> "0110083","arrhythmogenic right ventricular dysplasia 12","mondo","0012684"
> "0110082","arrhythmogenic right ventricular dysplasia 11","icd10cm","I42.8"
> "0110082","arrhythmogenic right ventricular dysplasia 11","mondo","0012506"
> "12339","retroperitoneal lymphoma","umls","C1335779"
> "12339","retroperitoneal lymphoma","mondo","0001499"
> "12335","male genital organ vascular disease","icd10cm","N50.1"
> "12335","male genital organ vascular disease","icd9cm","608.83"
> "12335","male genital organ vascular disease","umls","C0042374"
> "12335","male genital organ vascular disease","mondo","0001497"
> "12336","male infertility","icd10cm","N46"
> "12336","male infertility","icd10cm","N46.9"
> "12336","male infertility","icd9cm","606"
> "12336","male infertility","icd9cm","606.9"
> "12336","male infertility","mesh","D007248"
> "12336","male infertility","umls","C0021364"
> "12336","male infertility","mondo","0005372"
> "12337","varicocele","icd10cm","I86.1"
> "12337","varicocele","icd9cm","456.4"
> "12337","varicocele","mesh","D014646"
> "12337","varicocele","umls","C0042341"
> "12337","varicocele","mondo","0001498"
> "12332","hematocele of tunica vaginalis testis","mesh","D006398"
> "12332","hematocele of tunica vaginalis testis","umls","C0018931"
> "12332","hematocele of tunica vaginalis testis","mondo","0001495"
> "12333","male genital organ stricture","icd9cm","608.85"
> "12333","male genital organ stricture","umls","C0156316"
> "12333","male genital organ stricture","mondo","0001496"
> "7008","protoplasmic astrocytoma","mesh","D001254"
> "7008","protoplasmic astrocytoma","umls","C0334580"
> "7008","protoplasmic astrocytoma","mondo","0016687"
> "10242","ehrlichiosis","icd10cm","A77.4"
> "10242","ehrlichiosis","icd10cm","A77.40"
> "10242","ehrlichiosis","icd9cm","082.4"
> "10242","ehrlichiosis","icd9cm","082.40"
> "10242","ehrlichiosis","mesh","D016873"
> "10242","ehrlichiosis","umls","C0085399"
> "10242","ehrlichiosis","mondo","0016003"
> "9024","intestine carcinoma in situ","icd10cm","D01.4"
> "9024","intestine carcinoma in situ","icd9cm","230.7"
> "9024","intestine carcinoma in situ","umls","C0154065"
> "9024","intestine carcinoma in situ","mondo","0004698"
> "10241","thalassemia","icd10cm","D56"
> "10241","thalassemia","icd10cm","D56.9"
> "10241","thalassemia","icd9cm","282.4"
> "10241","thalassemia","icd9cm","282.40"
> "10241","thalassemia","mesh","D013789"
> "10241","thalassemia","umls","C0039730"
> "10241","thalassemia","mondo","0000984"
> "7005","gemistocytic astrocytoma","mesh","D001254"
> "7005","gemistocytic astrocytoma","umls","C0334581"
> "7005","gemistocytic astrocytoma","mondo","0016689"
> "7004","ACTH-secreting pituitary adenoma","mesh","D049913"
> "7004","ACTH-secreting pituitary adenoma","umls","C1306214"
> "7004","ACTH-secreting pituitary adenoma","mondo","0009050"
> "7007","childhood cerebral astrocytoma","mesh","D001254"
> "7007","childhood cerebral astrocytoma","umls","C0338070"
> "7007","childhood cerebral astrocytoma","mondo","0004071"
> "743","dermatographia","icd10cm","L50.3"
> "743","dermatographia","icd9cm","708.3"
> "743","dermatographia","umls","C0343065"
> "743","dermatographia","mondo","0007448"
> "745","epididymis adenomatoid tumor","umls","C1333415"
> "745","epididymis adenomatoid tumor","mondo","0004227"
> "746","adenomatoid tumor","icd10cm","D19.9"
> "746","adenomatoid tumor","mesh","D018254"
> "746","adenomatoid tumor","umls","C0206675"
> "746","adenomatoid tumor","mondo","0004230"
> "11693","acute apical periodontitis","icd10cm","K04.4"
> "11693","acute apical periodontitis","icd9cm","522.4"
> "11693","acute apical periodontitis","umls","C0155934"
> "11693","acute apical periodontitis","mondo","0001338"
> "2945","severe acute respiratory syndrome","icd10cm","J12.81"
> "2945","severe acute respiratory syndrome","icd9cm","079.82"
> "2945","severe acute respiratory syndrome","mesh","D045169"
> "2945","severe acute respiratory syndrome","umls","C1175175"
> "2945","severe acute respiratory syndrome","mondo","0005091"
> "2942","bronchiolitis","mesh","D001988"
> "2942","bronchiolitis","umls","C0006271"
> "2942","bronchiolitis","mondo","0002465"
> "0050858","Marshall-Smith syndrome","mesh","C536026"
> "0050858","Marshall-Smith syndrome","mondo","0011244"
> "5353","colonic disease","mesh","D003108"
> "5353","colonic disease","umls","C0009373"
> "5353","colonic disease","mondo","0003409"
> "5351","ovarian primitive germ cell tumor","umls","C1518727"
> "5351","ovarian primitive germ cell tumor","mondo","0003408"
> "5350","ovarian endodermal sinus tumor","umls","C0346188"
> "5350","ovarian endodermal sinus tumor","mondo","0006344"
> "1059","intellectual disability","mesh","D008607"
> "1059","intellectual disability","umls","C0025362"
> "1059","intellectual disability","mondo","0001071"
> "0050854","Muckle-Wells syndrome","mondo","0008633"
> "0050857","Perrault syndrome","mondo","0017312"
> "4310","smooth muscle tumor","mesh","D018235"
> "4310","smooth muscle tumor","umls","C0206658"
> "4310","smooth muscle tumor","mondo","0006975"
> "4313","epidermolysis bullosa acquisita","icd10cm","L12.3"
> "4313","epidermolysis bullosa acquisita","icd10cm","L12.30"
> "4313","epidermolysis bullosa acquisita","mesh","D016107"
> "4313","epidermolysis bullosa acquisita","umls","C0079293"
> "4313","epidermolysis bullosa acquisita","mondo","0018747"
> "11044","gastroschisis","icd10cm","Q79.3"
> "11044","gastroschisis","icd9cm","756.73"
> "11044","gastroschisis","mesh","D020139"
> "11044","gastroschisis","umls","C0265706"
> "11044","gastroschisis","mondo","0009264"
> "11042","Felty's syndrome","icd10cm","M05.0"
> "11042","Felty's syndrome","icd10cm","M05.00"
> "11042","Felty's syndrome","icd9cm","714.1"
> "11042","Felty's syndrome","mesh","D005258"
> "11042","Felty's syndrome","umls","C0015773"
> "11042","Felty's syndrome","mondo","0007603"
> "11049","meconium aspiration syndrome","icd10cm","P24.0"
> "11049","meconium aspiration syndrome","icd10cm","P24.00"
> "11049","meconium aspiration syndrome","icd10cm","P24.01"
> "11049","meconium aspiration syndrome","mesh","D008471"
> "11049","meconium aspiration syndrome","umls","C0025048"
> "11049","meconium aspiration syndrome","mondo","0006851"
> "2377","multiple sclerosis","icd10cm","G35"
> "2377","multiple sclerosis","icd9cm","340"
> "2377","multiple sclerosis","mesh","D009103"
> "2377","multiple sclerosis","umls","C0026769"
> "2377","multiple sclerosis","mondo","0005301"
> "3119","gastrointestinal system cancer","icd10cm","C26.9"
> "3119","gastrointestinal system cancer","icd9cm","239.0"
> "3119","gastrointestinal system cancer","mesh","D004067"
> "3119","gastrointestinal system cancer","mesh","D005770"
> "3119","gastrointestinal system cancer","umls","C0012243"
> "3119","gastrointestinal system cancer","umls","C0017185"
> "3119","gastrointestinal system cancer","umls","C0685938"
> "3119","gastrointestinal system cancer","mondo","0002516"
> "3118","hepatobiliary disease","umls","C0267792"
> "3118","hepatobiliary disease","mondo","0002515"
> "3117","hepatobiliary benign neoplasm","umls","C0854196"
> "3117","hepatobiliary benign neoplasm","mondo","0002514"
> "3116","kidney benign neoplasm","umls","C1334323"
> "3116","kidney benign neoplasm","mondo","0002513"
> "3114","serous cystadenocarcinoma","mesh","D018284"
> "3114","serous cystadenocarcinoma","umls","C0206701"
> "3114","serous cystadenocarcinoma","mondo","0005278"
> "3113","papillary carcinoma","mesh","D002291"
> "3113","papillary carcinoma","umls","C0007133"
> "3113","papillary carcinoma","mondo","0006509"
> "3112","papillary adenocarcinoma","mesh","D000231"
> "3112","papillary adenocarcinoma","umls","C0001420"
> "3112","papillary adenocarcinoma","umls","C1321863"
> "3112","papillary adenocarcinoma","mondo","0002512"
> "3111","cystadenocarcinoma","mesh","D003536"
> "3111","cystadenocarcinoma","umls","C0010631"
> "3111","cystadenocarcinoma","mondo","0005596"
> "3110","papillary cystadenocarcinoma","mesh","D018283"
> "3110","papillary cystadenocarcinoma","umls","C0206700"
> "3110","papillary cystadenocarcinoma","mondo","0005074"
> "8649","tongue cancer","icd10cm","C01"
> "8649","tongue cancer","icd10cm","C02.0"
> "8649","tongue cancer","icd10cm","C02.1"
> "8649","tongue cancer","icd10cm","C02.2"
> "8649","tongue cancer","icd10cm","C02.4"
> "8649","tongue cancer","icd10cm","C02.9"
> "8649","tongue cancer","icd9cm","141"
> "8649","tongue cancer","icd9cm","141.0"
> "8649","tongue cancer","icd9cm","141.1"
> "8649","tongue cancer","icd9cm","141.2"
> "8649","tongue cancer","icd9cm","141.3"
> "8649","tongue cancer","icd9cm","141.5"
> "8649","tongue cancer","icd9cm","141.6"
> "8649","tongue cancer","icd9cm","141.9"
> "8649","tongue cancer","mesh","D014062"
> "8649","tongue cancer","umls","C0153349"
> "8649","tongue cancer","umls","C0153350"
> "8649","tongue cancer","umls","C0153351"
> "8649","tongue cancer","umls","C0153356"
> "8649","tongue cancer","umls","C0474963"
> "8649","tongue cancer","umls","C0496755"
> "8649","tongue cancer","umls","C0684333"
> "8649","tongue cancer","mondo","0004631"
> "8646","substance-induced psychosis","icd9cm","293.89"
> "8646","substance-induced psychosis","umls","C0154334"
> "8646","substance-induced psychosis","mondo","0004630"
> "8644","gastroduodenitis","icd9cm","535.4"
> "8644","gastroduodenitis","umls","C0029800"
> "8644","gastroduodenitis","mondo","0004628"
> "8645","subacute delirium","icd9cm","293.1"
> "8645","subacute delirium","mesh","D003693"
> "8645","subacute delirium","umls","C0154333"
> "8645","subacute delirium","mondo","0004629"
> "8643","duodenitis","icd10cm","K29.8"
> "8643","duodenitis","icd9cm","535.6"
> "8643","duodenitis","mesh","D004382"
> "8643","duodenitis","umls","C0013298"
> "8643","duodenitis","mondo","0004627"
> "0060711","autosomal recessive congenital ichthyosis 3","icd10cm","Q80.2"
> "0060711","autosomal recessive congenital ichthyosis 3","mondo","0011680"
> "0060710","autosomal recessive congenital ichthyosis 2","icd10cm","Q80.2"
> "0060710","autosomal recessive congenital ichthyosis 2","mondo","0009439"
> "0060713","autosomal recessive congenital ichthyosis 4B","icd10cm","Q80.4"
> "0060713","autosomal recessive congenital ichthyosis 4B","mondo","0009443"
> "0060712","autosomal recessive congenital ichthyosis 4A","icd10cm","Q80.2"
> "0060712","autosomal recessive congenital ichthyosis 4A","mondo","0011026"
> "0060715","autosomal recessive congenital ichthyosis 6","icd10cm","Q80.2"
> "0060715","autosomal recessive congenital ichthyosis 6","mondo","0012847"
> "0060714","autosomal recessive congenital ichthyosis 5","icd10cm","Q80.2"
> "0060714","autosomal recessive congenital ichthyosis 5","mondo","0011485"
> "0060717","autosomal recessive congenital ichthyosis 8","icd10cm","Q80.2"
> "0060717","autosomal recessive congenital ichthyosis 8","mondo","0013495"
> "0060716","autosomal recessive congenital ichthyosis 7","icd10cm","Q80.2"
> "0060716","autosomal recessive congenital ichthyosis 7","mondo","0014009"
> "0060719","autosomal recessive congenital ichthyosis 10","icd10cm","Q80.2"
> "0060719","autosomal recessive congenital ichthyosis 10","mondo","0014011"
> "0060718","autosomal recessive congenital ichthyosis 9","icd10cm","Q80.2"
> "0060718","autosomal recessive congenital ichthyosis 9","mondo","0014010"
> "5740","small intestinal vasoactive intestinal peptide producing tumor","umls","C1336009"
> "5740","small intestinal vasoactive intestinal peptide producing tumor","mondo","0003621"
> "5741","pancreatic vasoactive intestinal peptide producing tumor","umls","C2033037"
> "5741","pancreatic vasoactive intestinal peptide producing tumor","mondo","0003622"
> "5742","pancreatic acinar cell adenocarcinoma","umls","C0279661"
> "5742","pancreatic acinar cell adenocarcinoma","mondo","0006346"
> "5743","acinic cell breast carcinoma","umls","C1515868"
> "5743","acinic cell breast carcinoma","mondo","0003624"
> "5744","ovary serous adenocarcinoma","umls","C1335177"
> "5744","ovary serous adenocarcinoma","umls","C1518234"
> "5744","ovary serous adenocarcinoma","mondo","0005211"
> "5746","ovarian serous cystadenocarcinoma","umls","C0279663"
> "5746","ovarian serous cystadenocarcinoma","mondo","0006046"
> "5747","uterine ligament serous adenocarcinoma","umls","C1519872"
> "5747","uterine ligament serous adenocarcinoma","mondo","0003626"
> "5748","rheumatic pulmonary valve disease","icd10cm","I09.89"
> "5748","rheumatic pulmonary valve disease","icd9cm","397.1"
> "5748","rheumatic pulmonary valve disease","umls","C0155579"
> "5748","rheumatic pulmonary valve disease","mondo","0003627"
> "5749","pulmonary valve disease","icd9cm","424.3"
> "5749","pulmonary valve disease","umls","C0034087"
> "5749","pulmonary valve disease","mondo","0003628"
> "11302","cercarial dermatitis","icd10cm","B65.3"
> "11302","cercarial dermatitis","icd9cm","120.3"
> "11302","cercarial dermatitis","umls","C0546996"
> "11302","cercarial dermatitis","mondo","0001260"
> "12731","pars planitis","icd10cm","H30.2"
> "12731","pars planitis","icd9cm","363.21"
> "12731","pars planitis","mesh","D015868"
> "12731","pars planitis","umls","C0030593"
> "12731","pars planitis","mondo","0011644"
> "1700","X-linked ichthyosis","icd10cm","Q80.1"
> "1700","X-linked ichthyosis","mesh","D016114"
> "1700","X-linked ichthyosis","umls","C0079588"
> "1700","X-linked ichthyosis","mondo","0010622"
> "14188","frozen shoulder","icd10cm","M75.0"
> "14188","frozen shoulder","icd9cm","726.0"
> "14188","frozen shoulder","mesh","D002062"
> "14188","frozen shoulder","umls","C0311223"
> "14188","frozen shoulder","mondo","0006763"
> "1702","ichthyosis vulgaris","icd10cm","Q80.0"
> "1702","ichthyosis vulgaris","mesh","D016112"
> "1702","ichthyosis vulgaris","umls","C0079584"
> "1702","ichthyosis vulgaris","mondo","0007810"
> "1703","Richter's syndrome","icd10cm","C91.1"
> "1703","Richter's syndrome","umls","C0349631"
> "1703","Richter's syndrome","mondo","0002083"
> "10193","classic type lipoma","umls","C1333059"
> "10193","classic type lipoma","mondo","0000967"
> "12531","von Willebrand's disease","icd10cm","D68.0"
> "12531","von Willebrand's disease","icd10cm","D69.8"
> "12531","von Willebrand's disease","icd9cm","286.4"
> "12531","von Willebrand's disease","mesh","D014842"
> "12531","von Willebrand's disease","umls","C0042974"
> "12531","von Willebrand's disease","mondo","0019565"
> "12733","hypercementosis","icd10cm","K03.4"
> "12733","hypercementosis","icd9cm","521.5"
> "12733","hypercementosis","mesh","D006936"
> "12733","hypercementosis","umls","C0020441"
> "12733","hypercementosis","mondo","0006790"
> "1875","impotence","mondo","0005362"
> "14731","Weaver syndrome","mesh","C562443"
> "14731","Weaver syndrome","umls","C0220765"
> "14731","Weaver syndrome","mondo","0010193"
> "0110427","dilated cardiomyopathy 1V","icd10cm","I42.0"
> "0110427","dilated cardiomyopathy 1V","mondo","0013373"
> "0110426","dilated cardiomyopathy 1D","icd10cm","I42.0"
> "0110426","dilated cardiomyopathy 1D","mondo","0011095"
> "12657","vestibulocochlear nerve disease","icd10cm","H93.3"
> "12657","vestibulocochlear nerve disease","icd10cm","H93.3X"
> "12657","vestibulocochlear nerve disease","icd9cm","388.5"
> "12657","vestibulocochlear nerve disease","mesh","D000160"
> "12657","vestibulocochlear nerve disease","umls","C0001163"
> "12657","vestibulocochlear nerve disease","mondo","0001563"
> "0110425","dilated cardiomyopathy 1A","mondo","0007269"
> "0110424","dilated cardiomyopathy 1CC","icd10cm","I42.0"
> "0110424","dilated cardiomyopathy 1CC","mondo","0013147"
> "10871","age related macular degeneration","icd10cm","H35.30"
> "10871","age related macular degeneration","icd9cm","362.50"
> "10871","age related macular degeneration","mesh","D008268"
> "10871","age related macular degeneration","umls","C0242383"
> "10871","age related macular degeneration","mondo","0005150"
> "0110423","dilated cardiomyopathy 1C","icd10cm","I42.0"
> "0110423","dilated cardiomyopathy 1C","mondo","0011094"
> "10873","Kuhnt-Junius degeneration","icd10cm","H35.32"
> "10873","Kuhnt-Junius degeneration","icd9cm","362.52"
> "10873","Kuhnt-Junius degeneration","umls","C0271084"
> "10873","Kuhnt-Junius degeneration","mondo","0005417"
> "0110422","autosomal recessive pericentral pigmentary retinopathy","icd10cm","H35.5"
> "0110422","autosomal recessive pericentral pigmentary retinopathy","mondo","0009987"
> "0110720","neuronal ceroid lipofuscinosis 4B","icd10cm","E75.4"
> "0110720","neuronal ceroid lipofuscinosis 4B","mondo","0008083"
> "0110421","late-adult onset retinitis pigmentosa","icd10cm","H35.5"
> "0110421","late-adult onset retinitis pigmentosa","mondo","0009984"
> "0110721","neuronal ceroid lipofuscinosis 1","icd10cm","E75.4"
> "0110721","neuronal ceroid lipofuscinosis 1","mondo","0009744"
> "0110420","dominant pericentral pigmentary retinopathy","icd10cm","H35.5"
> "0110420","dominant pericentral pigmentary retinopathy","mondo","0008381"
> "0110722","neuronal ceroid lipofuscinosis 7","icd10cm","E75.4"
> "0110722","neuronal ceroid lipofuscinosis 7","mondo","0012588"
> "0110723","neuronal ceroid lipofuscinosis 8","icd10cm","E75.4"
> "0110723","neuronal ceroid lipofuscinosis 8","mondo","0010830"
> "0110724","neuronal ceroid lipofuscinosis 8 northern epilepsy variant","icd10cm","E75.4"
> "0110724","neuronal ceroid lipofuscinosis 8 northern epilepsy variant","mondo","0012391"
> "2135","temporal lobe neoplasm","icd10cm","C71.2"
> "2135","temporal lobe neoplasm","icd9cm","191.2"
> "2135","temporal lobe neoplasm","umls","C0153636"
> "2135","temporal lobe neoplasm","umls","C1263887"
> "2135","temporal lobe neoplasm","mondo","0002218"
> "0110725","neuronal ceroid lipofuscinosis 10","icd10cm","E75.4"
> "0110725","neuronal ceroid lipofuscinosis 10","mondo","0012414"
> "0110726","neuronal ceroid lipofuscinosis 2","icd10cm","E75.4"
> "0110726","neuronal ceroid lipofuscinosis 2","mondo","0008769"
> "0110727","neuronal ceroid lipofuscinosis 13","icd10cm","E75.4"
> "0110727","neuronal ceroid lipofuscinosis 13","mondo","0014147"
> "0110728","neuronal ceroid lipofuscinosis 5","icd10cm","E75.4"
> "0110728","neuronal ceroid lipofuscinosis 5","mondo","0009745"
> "2378","relapsing-remitting multiple sclerosis","mesh","D020529"
> "2378","relapsing-remitting multiple sclerosis","umls","C0751967"
> "2378","relapsing-remitting multiple sclerosis","mondo","0005314"
> "0110729","neuronal ceroid lipofuscinosis 6","icd10cm","E75.4"
> "0110729","neuronal ceroid lipofuscinosis 6","mondo","0011144"
> "2132","brain sarcoma","umls","C1332607"
> "2132","brain sarcoma","mondo","0002216"
> "2373","hereditary elliptocytosis","icd10cm","D58.1"
> "2373","hereditary elliptocytosis","icd9cm","282.1"
> "2373","hereditary elliptocytosis","mesh","D004612"
> "2373","hereditary elliptocytosis","umls","C0013902"
> "2373","hereditary elliptocytosis","mondo","0017319"
> "0050529","adult spinal muscular atrophy","mondo","0010056"
> "1607","hypoglycemic coma","icd10cm","E15"
> "1607","hypoglycemic coma","icd9cm","251.0"
> "1607","hypoglycemic coma","umls","C0020617"
> "1607","hypoglycemic coma","mondo","0002053"
> "0050523","adult T-cell leukemia","icd10cm","C91.5"
> "0050523","adult T-cell leukemia","icd10cm","C91.50"
> "0050523","adult T-cell leukemia","mesh","D015459"
> "0050523","adult T-cell leukemia","umls","C0023493"
> "0050523","adult T-cell leukemia","mondo","0019471"
> "0050524","maturity-onset diabetes of the young","kegg","04950"
> "0050524","maturity-onset diabetes of the young","icd10cm","E11.8"
> "0050524","maturity-onset diabetes of the young","mondo","0018911"
> "0050526","Gamstorp-Wohlfart syndrome","mondo","0007646"
> "4944","gastroesophageal junction adenocarcinoma","umls","C1332166"
> "4944","gastroesophageal junction adenocarcinoma","mondo","0003219"
> "4947","cholangiocarcinoma","icd10cm","C22.1"
> "4947","cholangiocarcinoma","mesh","D018281"
> "4947","cholangiocarcinoma","umls","C0206698"
> "4947","cholangiocarcinoma","umls","C0280725"
> "4947","cholangiocarcinoma","mondo","0019087"
> "4943","adenocarcinoma in situ","mesh","D065311"
> "4943","adenocarcinoma in situ","umls","C0334276"
> "4943","adenocarcinoma in situ","mondo","0003218"
> "4948","gallbladder carcinoma","umls","C0235782"
> "4948","gallbladder carcinoma","mondo","0003220"
> "2112","cystoisosporiasis","icd10cm","A07.3"
> "2112","cystoisosporiasis","mesh","D021865"
> "2112","cystoisosporiasis","umls","C0311386"
> "2112","cystoisosporiasis","mondo","0018769"
> "2113","coccidiosis","mesh","D003048"
> "2113","coccidiosis","umls","C0009187"
> "2113","coccidiosis","mondo","0005707"
> "2115","B cell deficiency","icd9cm","279.03"
> "2115","B cell deficiency","umls","C0154276"
> "2115","B cell deficiency","mondo","0002211"
> "14022","algoneurodystrophy","icd10cm","M89.0"
> "14022","algoneurodystrophy","icd10cm","M89.00"
> "14022","algoneurodystrophy","icd9cm","733.7"
> "14022","algoneurodystrophy","umls","C0205930"
> "14022","algoneurodystrophy","mondo","0001859"
> "14021","Tietze's syndrome","icd10cm","M94.0"
> "14021","Tietze's syndrome","icd9cm","733.6"
> "14021","Tietze's syndrome","mesh","D013991"
> "14021","Tietze's syndrome","umls","C0040213"
> "14021","Tietze's syndrome","mondo","0001858"
> "14026","folic acid deficiency anemia","icd10cm","D52"
> "14026","folic acid deficiency anemia","icd10cm","D52.9"
> "14026","folic acid deficiency anemia","icd9cm","281.2"
> "14026","folic acid deficiency anemia","umls","C0151482"
> "14026","folic acid deficiency anemia","mondo","0001860"
> "1919","Lesch-Nyhan syndrome","icd10cm","E79.1"
> "1919","Lesch-Nyhan syndrome","mesh","D007926"
> "1919","Lesch-Nyhan syndrome","umls","C0023374"
> "1919","Lesch-Nyhan syndrome","mondo","0010298"
> "13709","premature ejaculation","icd10cm","F52.4"
> "13709","premature ejaculation","icd9cm","302.75"
> "13709","premature ejaculation","mesh","D061686"
> "13709","premature ejaculation","umls","C0033038"
> "13709","premature ejaculation","mondo","0001780"
> "1911","endodermal sinus tumor","mesh","D018240"
> "1911","endodermal sinus tumor","umls","C0014145"
> "1911","endodermal sinus tumor","mondo","0005744"
> "1910","vaginal yolk sac tumor","umls","C1336945"
> "1910","vaginal yolk sac tumor","mondo","0002143"
> "5100","middle ear disease","umls","C0271428"
> "5100","middle ear disease","mondo","0003276"
> "5101","auricular cancer","mesh","D004428"
> "5101","auricular cancer","umls","C0751094"
> "5101","auricular cancer","mondo","0003277"
> "3283","invasive malignant thymoma","umls","C0278846"
> "3283","invasive malignant thymoma","mondo","0002592"
> "3282","dendritic cell thymoma","umls","C1328042"
> "3282","dendritic cell thymoma","mondo","0016974"
> "5104","testicular infarct","umls","C0392041"
> "5104","testicular infarct","mondo","0003279"
> "3280","mixed type thymoma","umls","C1266092"
> "3280","mixed type thymoma","mondo","0016975"
> "14457","Brucella abortus brucellosis","icd10cm","A23.1"
> "14457","Brucella abortus brucellosis","icd9cm","023.1"
> "14457","Brucella abortus brucellosis","mesh","D002007"
> "14457","Brucella abortus brucellosis","umls","C0302363"
> "14457","Brucella abortus brucellosis","mondo","0001973"
> "13214","hole retinal cyst","icd10cm","H35.34"
> "13214","hole retinal cyst","icd9cm","362.54"
> "13214","hole retinal cyst","umls","C1261331"
> "13214","hole retinal cyst","mondo","0001663"
> "14324","Plasmodium malariae malaria","icd10cm","B52"
> "14324","Plasmodium malariae malaria","icd10cm","B52.9"
> "14324","Plasmodium malariae malaria","icd9cm","084.2"
> "14324","Plasmodium malariae malaria","umls","C0024536"
> "14324","Plasmodium malariae malaria","mondo","0001943"
> "10499","orbital granuloma","icd10cm","H05.11"
> "10499","orbital granuloma","icd9cm","376.11"
> "10499","orbital granuloma","umls","C0155262"
> "10499","orbital granuloma","mondo","0001048"
> "14453","farmer's lung","icd10cm","J67.0"
> "14453","farmer's lung","icd9cm","495.0"
> "14453","farmer's lung","mesh","D005203"
> "14453","farmer's lung","umls","C0015634"
> "14453","farmer's lung","mondo","0001971"
> "10493","adrenal cortical hypofunction","icd9cm","255.4"
> "10493","adrenal cortical hypofunction","umls","C0405580"
> "10493","adrenal cortical hypofunction","mondo","0000004"
> "14320","generalized anxiety disorder","icd10cm","F41.1"
> "14320","generalized anxiety disorder","icd9cm","300.02"
> "14320","generalized anxiety disorder","umls","C0270549"
> "14320","generalized anxiety disorder","mondo","0001942"
> "883","parasitic helminthiasis infectious disease","icd10cm","B65-B83"
> "883","parasitic helminthiasis infectious disease","icd10cm","B83.9"
> "883","parasitic helminthiasis infectious disease","icd9cm","120-129.99"
> "883","parasitic helminthiasis infectious disease","icd9cm","128.9"
> "883","parasitic helminthiasis infectious disease","mesh","D006373"
> "883","parasitic helminthiasis infectious disease","umls","C0018889"
> "883","parasitic helminthiasis infectious disease","mondo","0004664"
> "882","heterophyiasis","icd10cm","B66.8"
> "882","heterophyiasis","icd9cm","121.6"
> "882","heterophyiasis","umls","C0152071"
> "882","heterophyiasis","mondo","0004662"
> "14451","hyperkalemic periodic paralysis","icd10cm","G72.3"
> "14451","hyperkalemic periodic paralysis","mesh","D020513"
> "14451","hyperkalemic periodic paralysis","umls","C0238357"
> "14451","hyperkalemic periodic paralysis","mondo","0008224"
> "885","fascioliasis","icd10cm","B66.3"
> "885","fascioliasis","icd9cm","121.3"
> "885","fascioliasis","mesh","D005211"
> "885","fascioliasis","umls","C0015652"
> "885","fascioliasis","mondo","0004668"
> "884","metagonimiasis","icd10cm","B66.8"
> "884","metagonimiasis","icd9cm","121.5"
> "884","metagonimiasis","mesh","D014201"
> "884","metagonimiasis","umls","C0025530"
> "884","metagonimiasis","mondo","0004666"
> "14791","Leber congenital amaurosis","mesh","D057130"
> "14791","Leber congenital amaurosis","umls","C0339527"
> "14791","Leber congenital amaurosis","mondo","0018998"
> "888","fasciolopsiasis","icd10cm","B66.5"
> "888","fasciolopsiasis","icd9cm","121.4"
> "888","fasciolopsiasis","mesh","D014201"
> "888","fasciolopsiasis","umls","C0015656"
> "888","fasciolopsiasis","mondo","0004672"
> "14796","Dubowitz syndrome","icd10cm","Q87.1"
> "14796","Dubowitz syndrome","mesh","C535718"
> "14796","Dubowitz syndrome","umls","C0175691"
> "14796","Dubowitz syndrome","mondo","0009124"
> "13628","favism","icd10cm","D55.0"
> "13628","favism","mesh","D005236"
> "13628","favism","umls","C0015702"
> "13628","favism","mondo","0001761"
> "355","mast-cell sarcoma","icd10cm","C96.2"
> "355","mast-cell sarcoma","icd10cm","C96.22"
> "355","mast-cell sarcoma","icd9cm","202.6"
> "355","mast-cell sarcoma","mesh","D012515"
> "355","mast-cell sarcoma","umls","C0036221"
> "355","mast-cell sarcoma","mondo","0019024"
> "14737","craniofrontonasal syndrome","mesh","C536456"
> "14737","craniofrontonasal syndrome","umls","C0220767"
> "14737","craniofrontonasal syndrome","mondo","0010570"
> "1727","retinal vein occlusion","mesh","D012170"
> "1727","retinal vein occlusion","umls","C0035328"
> "1727","retinal vein occlusion","mondo","0006951"
> "7503","extrahepatic bile duct papillary adenoma","umls","C1333510"
> "7503","extrahepatic bile duct papillary adenoma","mondo","0004250"
> "6868","mediastinal malignant lymphoma","umls","C1334665"
> "6868","mediastinal malignant lymphoma","mondo","0004021"
> "6869","parasagittal meningioma","mesh","D008579"
> "6869","parasagittal meningioma","umls","C0751304"
> "6869","parasagittal meningioma","mondo","0004022"
> "6865","oxyphilic endometrial endometrioid adenocarcinoma","umls","C1518768"
> "6865","oxyphilic endometrial endometrioid adenocarcinoma","mondo","0004019"
> "6867","mediastinal gray zone lymphoma","umls","C1334657"
> "6867","mediastinal gray zone lymphoma","mondo","0004020"
> "0110272","cataract 40","icd10cm","Q12.0"
> "0110272","cataract 40","mondo","0010544"
> "0110273","autosomal dominant limb-girdle muscular dystrophy","icd10cm","G71.0"
> "0110273","autosomal dominant limb-girdle muscular dystrophy","mondo","0015151"
> "0110270","cataract 17 multiple types","icd10cm","Q12.0"
> "0110270","cataract 17 multiple types","mondo","0012688"
> "0110271","cataract 23","icd10cm","Q12.0"
> "0110271","cataract 23","mondo","0012489"
> "0110276","autosomal recessive limb-girdle muscular dystrophy type 2B","icd10cm","G71.0"
> "0110276","autosomal recessive limb-girdle muscular dystrophy type 2B","mondo","0009676"
> "0110277","autosomal recessive limb-girdle muscular dystrophy type 2C","icd10cm","G71.0"
> "0110277","autosomal recessive limb-girdle muscular dystrophy type 2C","mondo","0009677"
> "0110274","autosomal recessive limb-girdle muscular dystrophy","icd10cm","G71.0"
> "0110274","autosomal recessive limb-girdle muscular dystrophy","mondo","0015152"
> "0110275","autosomal recessive limb-girdle muscular dystrophy type 2A","icd10cm","G71.0"
> "0110275","autosomal recessive limb-girdle muscular dystrophy type 2A","mondo","0009675"
> "0110278","autosomal recessive limb-girdle muscular dystrophy type 2D","icd10cm","G71.0"
> "0110278","autosomal recessive limb-girdle muscular dystrophy type 2D","mondo","0011968"
> "0110279","autosomal recessive limb-girdle muscular dystrophy type 2E","icd10cm","G71.0"
> "0110279","autosomal recessive limb-girdle muscular dystrophy type 2E","mondo","0011423"
> "8255","vulva fibroepithelial polyp","umls","C1336978"
> "8255","vulva fibroepithelial polyp","mondo","0006620"
> "8251","adult pleomorphic rhabdomyosarcoma","umls","C1332211"
> "8251","adult pleomorphic rhabdomyosarcoma","mondo","0004513"
> "8252","chronic rhinitis","icd10cm","J31.0"
> "8252","chronic rhinitis","icd9cm","472.0"
> "8252","chronic rhinitis","umls","C0008711"
> "8252","chronic rhinitis","mondo","0004514"
> "664","angiokeratoma of Fordyce","umls","C0263639"
> "664","angiokeratoma of Fordyce","mondo","0003954"
> "663","scrotal angioma","umls","C1335936"
> "663","scrotal angioma","mondo","0003951"
> "660","adrenal cortex cancer","icd10cm","C74.0"
> "660","adrenal cortex cancer","mesh","D000306"
> "660","adrenal cortex cancer","umls","C0001618"
> "660","adrenal cortex cancer","umls","C0346402"
> "660","adrenal cortex cancer","mondo","0006639"
> "5102","inner ear cancer","umls","C1512779"
> "5102","inner ear cancer","mondo","0003278"
> "8781","rubella","icd10cm","B06"
> "8781","rubella","icd10cm","B06.9"
> "8781","rubella","icd9cm","056"
> "8781","rubella","mesh","D012409"
> "8781","rubella","umls","C0035920"
> "8781","rubella","mondo","0004656"
> "8787","disseminated chorioretinitis","icd10cm","H30.1"
> "8787","disseminated chorioretinitis","icd10cm","H30.10"
> "8787","disseminated chorioretinitis","icd9cm","363.1"
> "8787","disseminated chorioretinitis","icd9cm","363.10"
> "8787","disseminated chorioretinitis","umls","C0154879"
> "8787","disseminated chorioretinitis","mondo","0004657"
> "0040100","Hirata disease","umls","C0854359"
> "0040100","Hirata disease","mondo","0018465"
> "3284","thymic carcinoma","mesh","D013945"
> "3284","thymic carcinoma","umls","C0205969"
> "3284","thymic carcinoma","mondo","0006451"
> "7614","meninges sarcoma","umls","C0302327"
> "7614","meninges sarcoma","mondo","0004308"
> "7615","sarcomatosis","umls","C0334451"
> "7615","sarcomatosis","mondo","0004309"
> "7610","mixed cell type adenoma of parathyroid","umls","C0279701"
> "7610","mixed cell type adenoma of parathyroid","mondo","0004304"
> "7611","parathyroid oncocytic adenoma","umls","C1335351"
> "7611","parathyroid oncocytic adenoma","mondo","0004305"
> "7612","childhood intracortical osteosarcoma","umls","C1332974"
> "7612","childhood intracortical osteosarcoma","mondo","0004306"
> "7613","sarcomatosis of the meninges","umls","C0334612"
> "7613","sarcomatosis of the meninges","mondo","0004307"
> "8431","physiological polycythemia","umls","C0856817"
> "8431","physiological polycythemia","mondo","0004563"
> "8433","thyroid malformation","umls","C0877367"
> "8433","thyroid malformation","mondo","0004564"
> "8432","polycythemia","icd10cm","D75.1"
> "8432","polycythemia","mesh","D011086"
> "8432","polycythemia","umls","C0032461"
> "8432","polycythemia","mondo","0005571"
> "8437","intestinal obstruction","icd10cm","K56.60"
> "8437","intestinal obstruction","icd10cm","K56.609"
> "8437","intestinal obstruction","icd10cm","K56.69"
> "8437","intestinal obstruction","icd9cm","560.9"
> "8437","intestinal obstruction","mesh","D007415"
> "8437","intestinal obstruction","umls","C0021843"
> "8437","intestinal obstruction","mondo","0004565"
> "8439","postgastrectomy syndrome","icd10cm","K91.1"
> "8439","postgastrectomy syndrome","icd9cm","564.2"
> "8439","postgastrectomy syndrome","mesh","D011178"
> "8439","postgastrectomy syndrome","umls","C0032763"
> "8439","postgastrectomy syndrome","mondo","0004566"
> "8438","afferent loop syndrome","mesh","D000343"
> "8438","afferent loop syndrome","umls","C0001727"
> "8438","afferent loop syndrome","mondo","0006641"
> "9827","radioulnar synostosis","icd10cm","Q74.0"
> "9827","radioulnar synostosis","icd9cm","755.53"
> "9827","radioulnar synostosis","mesh","C562408"
> "9827","radioulnar synostosis","umls","C0158761"
> "9827","radioulnar synostosis","mondo","0017985"
> "9821","choroideremia","icd10cm","H31.21"
> "9821","choroideremia","icd9cm","363.55"
> "9821","choroideremia","mesh","D015794"
> "9821","choroideremia","umls","C0008525"
> "9821","choroideremia","mondo","0010557"
> "9820","central gyrate choroidal dystrophy","icd9cm","363.54"
> "9820","central gyrate choroidal dystrophy","umls","C0154898"
> "9820","central gyrate choroidal dystrophy","mondo","0004889"
> "9822","partial central choroid dystrophy","icd9cm","363.53"
> "9822","partial central choroid dystrophy","umls","C0339427"
> "9822","partial central choroid dystrophy","mondo","0004890"
> "9828","neonatal abstinence syndrome","icd10cm","P96.1"
> "9828","neonatal abstinence syndrome","icd9cm","779.5"
> "9828","neonatal abstinence syndrome","mesh","D009357"
> "9828","neonatal abstinence syndrome","umls","C0027609"
> "9828","neonatal abstinence syndrome","umls","C1332133"
> "9828","neonatal abstinence syndrome","mondo","0005566"
> "0080240","X-linked mental retardation 106","mondo","0030907"
> "12594","Potter's syndrome","icd10cm","Q60.6"
> "12594","Potter's syndrome","umls","C0178426"
> "12594","Potter's syndrome","mondo","0001558"
> "8514","acute pulmonary heart disease","icd9cm","415"
> "8514","acute pulmonary heart disease","umls","C0155671"
> "8514","acute pulmonary heart disease","mondo","0004595"
> "8043","chest wall parachordoma","umls","C1332934"
> "8043","chest wall parachordoma","mondo","0004443"
> "4123","nail disease","icd10cm","L60"
> "4123","nail disease","icd10cm","L60.9"
> "4123","nail disease","icd9cm","703"
> "4123","nail disease","icd9cm","703.9"
> "4123","nail disease","mesh","D009260"
> "4123","nail disease","umls","C0027339"
> "4123","nail disease","mondo","0002884"
> "13868","hypoactive sexual desire disorder","icd10cm","F52.0"
> "13868","hypoactive sexual desire disorder","icd9cm","302.71"
> "13868","hypoactive sexual desire disorder","mesh","D020018"
> "13868","hypoactive sexual desire disorder","umls","C0020594"
> "13868","hypoactive sexual desire disorder","mondo","0001821"
> "13884","sick sinus syndrome","icd10cm","I49.5"
> "13884","sick sinus syndrome","mesh","D012804"
> "13884","sick sinus syndrome","umls","C0037052"
> "13884","sick sinus syndrome","mondo","0001823"
> "0060449","gelatinous drop-like corneal dystrophy","mesh","C535480"
> "0060449","gelatinous drop-like corneal dystrophy","umls","C0339273"
> "0060449","gelatinous drop-like corneal dystrophy","mondo","0008777"
> "5688","Werner syndrome","mesh","D014898"
> "5688","Werner syndrome","umls","C0043119"
> "5688","Werner syndrome","mondo","0010196"
> "13866","multiple cranial nerve palsy","icd10cm","G52.7"
> "13866","multiple cranial nerve palsy","icd9cm","352.6"
> "13866","multiple cranial nerve palsy","umls","C0154733"
> "13866","multiple cranial nerve palsy","mondo","0001819"
> "5684","spondyloepimetaphyseal dysplasia, Sponastrime type","umls","C0920349"
> "5684","spondyloepimetaphyseal dysplasia, Sponastrime type","mondo","0010068"
> "5681","ovarian embryonal carcinoma","umls","C0346183"
> "5681","ovarian embryonal carcinoma","mondo","0003581"
> "5680","embryonal testis carcinoma","umls","C0238448"
> "5680","embryonal testis carcinoma","mondo","0006446"
> "5683","hereditary breast ovarian cancer syndrome","mesh","D061325"
> "5683","hereditary breast ovarian cancer syndrome","umls","C0677776"
> "5683","hereditary breast ovarian cancer syndrome","mondo","0003582"
> "0080148","T-cell childhood lymphoblastic lymphoma","mondo","0000874"
> "0080149","adult acute monocytic leukemia","mondo","0000875"
> "0080142","mosaic variegated aneuploidy syndrome 2","mondo","0013582"
> "0080143","congenital fibrosis of the extraocular muscles","mondo","0007614"
> "0080140","multiple congenital anomalies-hypotonia-seizures syndrome 3","mondo","0014165"
> "0080141","mosaic variegated aneuploidy syndrome 1","mondo","0009759"
> "0080146","B-cell childhood acute lymphoblastic leukemia","mondo","0000872"
> "0080147","lymphoblastic lymphoma","mondo","0000873"
> "0080144","childhood acute lymphocytic leukemia","mondo","0000870"
> "0080145","T-cell childhood acute lymphocytic leukemia","mondo","0000871"
> "13561","optic disk drusen","icd10cm","H47.32"
> "13561","optic disk drusen","icd9cm","377.21"
> "13561","optic disk drusen","mesh","D015594"
> "13561","optic disk drusen","umls","C0029128"
> "13561","optic disk drusen","mondo","0001746"
> "11518","abnormal pupillary function","icd10cm","H57.09"
> "11518","abnormal pupillary function","icd9cm","379.49"
> "11518","abnormal pupillary function","umls","C0155376"
> "11518","abnormal pupillary function","mondo","0001303"
> "11514","fissured tongue","icd10cm","K14.5"
> "11514","fissured tongue","icd9cm","529.5"
> "11514","fissured tongue","mesh","D014063"
> "11514","fissured tongue","umls","C0040412"
> "11514","fissured tongue","mondo","0007655"
> "11516","hypertensive heart disease","icd10cm","I11"
> "11516","hypertensive heart disease","icd10cm","I11.9"
> "11516","hypertensive heart disease","icd9cm","402"
> "11516","hypertensive heart disease","icd9cm","402.9"
> "11516","hypertensive heart disease","umls","C0152105"
> "11516","hypertensive heart disease","mondo","0001302"
> "11512","Budd-Chiari syndrome","icd10cm","I82.0"
> "11512","Budd-Chiari syndrome","mesh","D006502"
> "11512","Budd-Chiari syndrome","umls","C0019154"
> "11512","Budd-Chiari syndrome","mondo","0006786"
> "5973","kidney pelvis papillary carcinoma","umls","C1377909"
> "5973","kidney pelvis papillary carcinoma","mondo","0003716"
> "5977","renal pelvis neoplasm","umls","C0346260"
> "5977","renal pelvis neoplasm","mondo","0003719"
> "5976","occlusion precerebral artery","icd10cm","I65.9"
> "5976","occlusion precerebral artery","icd9cm","433"
> "5976","occlusion precerebral artery","icd9cm","433.9"
> "5976","occlusion precerebral artery","umls","C0155727"
> "5976","occlusion precerebral artery","mondo","0003718"
> "5975","renal pelvis papillary tumor","umls","C0853688"
> "5975","renal pelvis papillary tumor","mondo","0003717"
> "5974","renal pelvis transitional cell carcinoma","umls","C0238410"
> "5974","renal pelvis transitional cell carcinoma","mondo","0005221"
> "14798","Blount's disease","mesh","C536237"
> "14798","Blount's disease","umls","C0220757"
> "14798","Blount's disease","mondo","0017194"
> "13431","bejel","mesh","D014211"
> "13431","bejel","umls","C0004945"
> "13431","bejel","mondo","0001714"
> "0090068","giant axonal neuropathy 1","mesh","D056768"
> "0090068","giant axonal neuropathy 1","mondo","0009749"
> "0090069","giant axonal neuropathy 2","mondo","0012411"
> "0090060","Wolcott-Rallison syndrome","icd10cm","E13"
> "0090060","Wolcott-Rallison syndrome","mesh","C536739"
> "0090060","Wolcott-Rallison syndrome","mondo","0009192"
> "0090061","familial cold autoinflammatory syndrome","icd10cm","L50.2"
> "0090061","familial cold autoinflammatory syndrome","mondo","0018768"
> "0090062","familial cold autoinflammatory syndrome 1","icd10cm","L50.2"
> "0090062","familial cold autoinflammatory syndrome 1","mondo","0007349"
> "0090063","familial cold autoinflammatory syndrome 2","mesh","C567090"
> "0090063","familial cold autoinflammatory syndrome 2","umls","C2673198"
> "0090063","familial cold autoinflammatory syndrome 2","mondo","0012724"
> "0090064","familial cold autoinflammatory syndrome 3","icd10cm","L50.2"
> "0090064","familial cold autoinflammatory syndrome 3","mondo","0013766"
> "0090065","familial cold autoinflammatory syndrome 4","icd10cm","L50.2"
> "0090065","familial cold autoinflammatory syndrome 4","mondo","0014498"
> "0090066","Fanconi-like syndrome","mondo","0009217"
> "0090067","Fuhrmann syndrome","icd10cm","Q74.8"
> "0090067","Fuhrmann syndrome","mesh","C538189"
> "0090067","Fuhrmann syndrome","mondo","0009232"
> "14793","hypohidrotic ectodermal dysplasia","mesh","D053358"
> "14793","hypohidrotic ectodermal dysplasia","umls","C0162359"
> "14793","hypohidrotic ectodermal dysplasia","mondo","0016535"
> "2583","agammaglobulinemia","icd10cm","D80.1"
> "2583","agammaglobulinemia","icd9cm","279.00"
> "2583","agammaglobulinemia","mesh","D000361"
> "2583","agammaglobulinemia","umls","C0001768"
> "2583","agammaglobulinemia","umls","C0086438"
> "2583","agammaglobulinemia","mondo","0015977"
> "2582","acatalasia","mesh","D020642"
> "2582","acatalasia","umls","C0268419"
> "2582","acatalasia","mondo","0013571"
> "2581","chondrodysplasia punctata","icd10cm","Q77.3"
> "2581","chondrodysplasia punctata","mesh","D002806"
> "2581","chondrodysplasia punctata","umls","C0008445"
> "2581","chondrodysplasia punctata","mondo","0019701"
> "2580","rhizomelic chondrodysplasia punctata","icd10cm","E71.540"
> "2580","rhizomelic chondrodysplasia punctata","mesh","D018902"
> "2580","rhizomelic chondrodysplasia punctata","umls","C0282529"
> "2580","rhizomelic chondrodysplasia punctata","mondo","0015776"
> "0110719","Warburg micro syndrome 4","icd10cm","Q87.0"
> "0110719","Warburg micro syndrome 4","mondo","0014296"
> "0110718","Warburg micro syndrome 3","icd10cm","Q87.0"
> "0110718","Warburg micro syndrome 3","mondo","0013638"
> "0060898","Parkinson's disease 20","mondo","0014233"
> "0110868","congenital stationary night blindness 1D","mondo","0013450"
> "0060896","Parkinson's disease 23","icd10cm","G20"
> "0060896","Parkinson's disease 23","mondo","0014796"
> "0060897","Parkinson's disease 17","mondo","0013625"
> "0060894","early-onset Parkinson's disease","mondo","0017279"
> "0060895","Parkinson's disease 4","icd10cm","G20"
> "0060895","Parkinson's disease 4","mondo","0011562"
> "0060892","late onset Parkinson's disease","mondo","0018466"
> "0110710","hypotrichosis 13","mondo","0014390"
> "0060890","ectopic Cushing syndrome","icd10cm","E24.3"
> "0060890","ectopic Cushing syndrome","mondo","0020527"
> "0060891","Parkinson's disease 19A","icd10cm","G20"
> "0060891","Parkinson's disease 19A","mondo","0014231"
> "6059","nasal vestibule papilloma","umls","C0339826"
> "6059","nasal vestibule papilloma","mondo","0003753"
> "6054","frontal sinus Schneiderian papilloma","umls","C1333645"
> "6054","frontal sinus Schneiderian papilloma","mondo","0003752"
> "6050","esophageal disease","icd10cm","K22.9"
> "6050","esophageal disease","icd9cm","530"
> "6050","esophageal disease","icd9cm","530.9"
> "6050","esophageal disease","mesh","D004935"
> "6050","esophageal disease","umls","C0014852"
> "6050","esophageal disease","mondo","0003749"
> "6053","pediatric germ cell cancer","umls","C0279014"
> "6053","pediatric germ cell cancer","mondo","0003751"
> "6052","central nervous system childhood germ cell tumor","umls","C0278754"
> "6052","central nervous system childhood germ cell tumor","mondo","0003750"
> "2639","breast pericanalicular fibroadenoma","umls","C0334497"
> "2639","breast pericanalicular fibroadenoma","mondo","0002371"
> "10003","sensorineural hearing loss","icd10cm","H90.5"
> "10003","sensorineural hearing loss","icd10cm","H91.9"
> "10003","sensorineural hearing loss","icd9cm","389.1"
> "10003","sensorineural hearing loss","icd9cm","389.10"
> "10003","sensorineural hearing loss","icd9cm","389.14"
> "10003","sensorineural hearing loss","mesh","D006313"
> "10003","sensorineural hearing loss","mesh","D006316"
> "10003","sensorineural hearing loss","mesh","D006319"
> "10003","sensorineural hearing loss","umls","C0018776"
> "10003","sensorineural hearing loss","umls","C0018780"
> "10003","sensorineural hearing loss","umls","C0018784"
> "10003","sensorineural hearing loss","mondo","0010576"
> "2634","cystadenoma","mesh","D003537"
> "2634","cystadenoma","umls","C0010633"
> "2634","cystadenoma","mondo","0002369"
> "0111404","Jalili syndrome","umls","C3495589"
> "2636","ovarian Brenner tumor","mesh","D001948"
> "2636","ovarian Brenner tumor","umls","C0006160"
> "2636","ovarian Brenner tumor","mondo","0002370"
> "0111402","mucopolysaccharidosis type IIID","umls","C0086650"
> "0111400","congenital dyserythropoietic anemia type IV","umls","C3150926"
> "2632","papillary serous adenocarcinoma","umls","C0334359"
> "2632","papillary serous adenocarcinoma","umls","C0334361"
> "2632","papillary serous adenocarcinoma","mondo","0002368"
> "9599","proliferative fasciitis","umls","C0432528"
> "9599","proliferative fasciitis","mondo","0004831"
> "9598","fasciitis","icd10cm","M72.9"
> "9598","fasciitis","icd9cm","729.4"
> "9598","fasciitis","mesh","D005208"
> "9598","fasciitis","umls","C0015645"
> "9598","fasciitis","mondo","0004830"
> "9597","Krukenberg carcinoma","mesh","D007725"
> "9597","Krukenberg carcinoma","umls","C0022790"
> "9597","Krukenberg carcinoma","mondo","0004829"
> "9590","lower urinary tract calculus","icd10cm","N21"
> "9590","lower urinary tract calculus","icd10cm","N21.9"
> "9590","lower urinary tract calculus","icd9cm","594"
> "9590","lower urinary tract calculus","icd9cm","594.9"
> "9590","lower urinary tract calculus","umls","C0156264"
> "9590","lower urinary tract calculus","mondo","0004828"
> "9220","central sleep apnea","mesh","D020182"
> "9220","central sleep apnea","umls","C0520680"
> "9220","central sleep apnea","mondo","0004731"
> "12358","patulous eustachian tube","icd10cm","H69.0"
> "12358","patulous eustachian tube","icd10cm","H69.00"
> "12358","patulous eustachian tube","icd9cm","381.7"
> "12358","patulous eustachian tube","umls","C0155434"
> "12358","patulous eustachian tube","mondo","0001508"
> "12359","endocrine exophthalmos","icd9cm","376.2"
> "12359","endocrine exophthalmos","umls","C0155264"
> "12359","endocrine exophthalmos","mondo","0001509"
> "12351","alcoholic hepatitis","icd9cm","571.1"
> "12351","alcoholic hepatitis","umls","C0001306"
> "12351","alcoholic hepatitis","mondo","0001505"
> "12357","viral labyrinthitis","icd9cm","386.35"
> "12357","viral labyrinthitis","umls","C0155508"
> "12357","viral labyrinthitis","mondo","0001507"
> "12355","prostatocystitis","icd10cm","N41.3"
> "12355","prostatocystitis","icd9cm","601.3"
> "12355","prostatocystitis","umls","C0156291"
> "12355","prostatocystitis","mondo","0001506"
> "10261","discharging ear","icd10cm","H92.1"
> "10261","discharging ear","icd10cm","H92.10"
> "10261","discharging ear","icd9cm","388.6"
> "10261","discharging ear","icd9cm","388.60"
> "10261","discharging ear","umls","C0155540"
> "10261","discharging ear","mondo","0000988"
> "10264","mumps","icd10cm","B26"
> "10264","mumps","icd10cm","B26.9"
> "10264","mumps","icd9cm","072"
> "10264","mumps","mesh","D009107"
> "10264","mumps","umls","C0026780"
> "10264","mumps","mondo","0000989"
> "10266","subendocardial infarction acute myocardial infarction","icd9cm","410.7"
> "10266","subendocardial infarction acute myocardial infarction","umls","C0155655"
> "10266","subendocardial infarction acute myocardial infarction","mondo","0000990"
> "2079","eccrine mixed tumor of skin","umls","C0346026"
> "2079","eccrine mixed tumor of skin","mondo","0002200"
> "9043","uterine cervix leukoplakia","icd10cm","N88.0"
> "9043","uterine cervix leukoplakia","icd9cm","622.2"
> "9043","uterine cervix leukoplakia","umls","C0269194"
> "9043","uterine cervix leukoplakia","mondo","0004702"
> "9042","polyp of corpus uteri","icd10cm","N84.0"
> "9042","polyp of corpus uteri","icd9cm","621.0"
> "9042","polyp of corpus uteri","umls","C0156369"
> "9042","polyp of corpus uteri","mondo","0004701"
> "3544","atypical choroid plexus papilloma","umls","C1266176"
> "3544","atypical choroid plexus papilloma","mondo","0002684"
> "3545","childhood choroid plexus cancer","umls","C0280623"
> "3545","childhood choroid plexus cancer","mondo","0002685"
> "3540","choroid plexus cancer","mesh","D016545"
> "3540","choroid plexus cancer","umls","C0085138"
> "3540","choroid plexus cancer","mondo","0002681"
> "3541","cerebral ventricle cancer","icd10cm","C71.5"
> "3541","cerebral ventricle cancer","icd9cm","191.5"
> "3541","cerebral ventricle cancer","mesh","D002551"
> "3541","cerebral ventricle cancer","umls","C0007798"
> "3541","cerebral ventricle cancer","umls","C0346906"
> "3541","cerebral ventricle cancer","mondo","0002682"
> "3542","adult choroid plexus cancer","umls","C0796430"
> "3542","adult choroid plexus cancer","mondo","0002683"
> "2965","bursitis","icd10cm","M71.9"
> "2965","bursitis","mesh","D002062"
> "2965","bursitis","umls","C0006444"
> "2965","bursitis","mondo","0002471"
> "2964","periarthritis","icd10cm","M77.9"
> "2964","periarthritis","mesh","D010489"
> "2964","periarthritis","umls","C0031037"
> "2964","periarthritis","mondo","0006898"
> "768","retinoblastoma","mesh","D012175"
> "768","retinoblastoma","umls","C0035335"
> "768","retinoblastoma","mondo","0008380"
> "769","neuroblastoma","mesh","D009447"
> "769","neuroblastoma","umls","C0027819"
> "769","neuroblastoma","mondo","0005072"
> "2960","photosensitive trichothiodystrophy","mesh","D054463"
> "2960","photosensitive trichothiodystrophy","umls","C1955934"
> "2960","photosensitive trichothiodystrophy","mondo","0002470"
> "2962","Cockayne syndrome","icd10cm","Q87.1"
> "2962","Cockayne syndrome","mesh","D003057"
> "2962","Cockayne syndrome","umls","C0009207"
> "2962","Cockayne syndrome","mondo","0016006"
> "767","muscular atrophy","mesh","D009133"
> "767","muscular atrophy","umls","C0026846"
> "767","muscular atrophy","mondo","0004323"
> "0050833","orotic aciduria","mondo","0009797"
> "0050831","familial encephalopathy with neuroserpin inclusion bodies","mesh","C536841"
> "0050831","familial encephalopathy with neuroserpin inclusion bodies","mondo","0011412"
> "0050830","peripheral artery disease","mesh","D058729"
> "0050830","peripheral artery disease","mondo","0005386"
> "0050836","focal dystonia","mondo","0000477"
> "0050835","generalized dystonia","icd10cm","G24.1"
> "0050835","generalized dystonia","icd10cm","G24.2"
> "0050835","generalized dystonia","icd9cm","333.6"
> "0050835","generalized dystonia","icd9cm","333.8"
> "0050835","generalized dystonia","mesh","D004422"
> "0050835","generalized dystonia","mesh","D020821"
> "0050835","generalized dystonia","umls","C0013423"
> "0050835","generalized dystonia","umls","C0154674"
> "0050835","generalized dystonia","umls","C0154675"
> "0050835","generalized dystonia","umls","C0393598"
> "0050835","generalized dystonia","umls","C0393601"
> "0050835","generalized dystonia","umls","C0752207"
> "0050835","generalized dystonia","mondo","0000476"
> "0050834","CHARGE syndrome","mesh","D058747"
> "0050834","CHARGE syndrome","umls","C0265354"
> "0050834","CHARGE syndrome","umls","C2936502"
> "0050834","CHARGE syndrome","mondo","0008965"
> "5379","hemoglobin E disease","icd10cm","D58.2"
> "5379","hemoglobin E disease","umls","C0238159"
> "5379","hemoglobin E disease","mondo","0016243"
> "5378","hemoglobin D disease","icd10cm","D58.2"
> "5378","hemoglobin D disease","umls","C0272080"
> "5378","hemoglobin D disease","mondo","0019537"
> "1079","setariasis","mesh","D012719"
> "1079","setariasis","umls","C0036850"
> "1079","setariasis","mondo","0005957"
> "5375","hair follicle neoplasm","umls","C0859920"
> "5375","hair follicle neoplasm","mondo","0003413"
> "5374","pilomatrixoma","mesh","D018296"
> "5374","pilomatrixoma","umls","C0206711"
> "5374","pilomatrixoma","mondo","0007564"
> "1074","kidney failure","icd10cm","N19"
> "1074","kidney failure","icd9cm","586"
> "1074","kidney failure","mesh","D051437"
> "1074","kidney failure","umls","C0035078"
> "1074","kidney failure","mondo","0001106"
> "5376","skin pilomatrix carcinoma","umls","C0585475"
> "5376","skin pilomatrix carcinoma","mondo","0003414"
> "5370","breast hemangiopericytoma","umls","C1511313"
> "5370","breast hemangiopericytoma","mondo","0003411"
> "5373","retroperitoneal hemangiopericytoma","umls","C1335777"
> "5373","retroperitoneal hemangiopericytoma","mondo","0003412"
> "13005","intra-abdominal lymph node mast cell malignancy","icd9cm","202.63"
> "13005","intra-abdominal lymph node mast cell malignancy","umls","C0153844"
> "13005","intra-abdominal lymph node mast cell malignancy","mondo","0001614"
> "13001","carotid stenosis","mesh","D016893"
> "13001","carotid stenosis","umls","C0007282"
> "13001","carotid stenosis","mondo","0001612"
> "13003","vertebrobasilar insufficiency","icd10cm","G45.0"
> "13003","vertebrobasilar insufficiency","icd9cm","435.3"
> "13003","vertebrobasilar insufficiency","mesh","D014715"
> "13003","vertebrobasilar insufficiency","umls","C0042568"
> "13003","vertebrobasilar insufficiency","mondo","0001613"
> "13002","subclavian steal syndrome","icd9cm","435.2"
> "13002","subclavian steal syndrome","mesh","D013349"
> "13002","subclavian steal syndrome","umls","C0038531"
> "13002","subclavian steal syndrome","mondo","0006983"
> "4336","tinea favosa","icd10cm","B35"
> "4336","tinea favosa","mesh","D014007"
> "4336","tinea favosa","umls","C0040254"
> "4336","tinea favosa","mondo","0005983"
> "4337","tinea capitis","icd9cm","110.0"
> "4337","tinea capitis","mesh","D014006"
> "4337","tinea capitis","umls","C0011640"
> "4337","tinea capitis","mondo","0002967"
> "4334","splenic manifestation of prolymphocytic leukemia","umls","C1336066"
> "4334","splenic manifestation of prolymphocytic leukemia","mondo","0002966"
> "4333","parovarian cyst","icd10cm","Q50.4"
> "4333","parovarian cyst","icd10cm","Q50.5"
> "4333","parovarian cyst","mesh","D010310"
> "4333","parovarian cyst","umls","C0030584"
> "4333","parovarian cyst","mondo","0002965"
> "4330","non-Langerhans-cell histiocytosis","mesh","D015616"
> "4330","non-Langerhans-cell histiocytosis","umls","C0019624"
> "4330","non-Langerhans-cell histiocytosis","mondo","0015531"
> "4331","burning mouth syndrome","mesh","D002054"
> "4331","burning mouth syndrome","umls","C0006430"
> "4331","burning mouth syndrome","mondo","0006687"
> "3134","facial dermatosis","mesh","D005148"
> "3134","facial dermatosis","umls","C0015456"
> "3134","facial dermatosis","mondo","0006548"
> "3136","scalp dermatosis","mesh","D012536"
> "3136","scalp dermatosis","umls","C0036271"
> "3136","scalp dermatosis","mondo","0006605"
> "3133","acute porphyria","mesh","D017094"
> "3133","acute porphyria","umls","C0162533"
> "3133","acute porphyria","mondo","0002520"
> "3132","porphyria cutanea tarda","icd10cm","E80.1"
> "3132","porphyria cutanea tarda","mesh","D017119"
> "3132","porphyria cutanea tarda","umls","C0162566"
> "3132","porphyria cutanea tarda","mondo","0015104"
> "13774","Addison's disease","icd10cm","E27.1"
> "13774","Addison's disease","mesh","D000224"
> "13774","Addison's disease","umls","C0001403"
> "13774","Addison's disease","mondo","0009410"
> "3138","acanthosis nigricans","icd10cm","L83"
> "3138","acanthosis nigricans","mesh","D000052"
> "3138","acanthosis nigricans","umls","C0000889"
> "3138","acanthosis nigricans","mondo","0007035"
> "13375","temporal arteritis","icd9cm","446.5"
> "13375","temporal arteritis","mesh","D013700"
> "13375","temporal arteritis","umls","C0039483"
> "13375","temporal arteritis","mondo","0008538"
> "0060779","congenital malabsorptive diarrhea 4","icd10cm","P78.3"
> "0060779","congenital malabsorptive diarrhea 4","mondo","0012479"
> "0060778","congenital diarrhea 7 with exudative enteropathy","icd10cm","P78.3"
> "0060778","congenital diarrhea 7 with exudative enteropathy","mondo","0014375"
> "0060773","cleft lip-palate-ectodermal dysplasia syndrome","mondo","0009151"
> "0060772","dextro-looped transposition of the great arteries 3","icd10cm","Q20.3"
> "0060772","dextro-looped transposition of the great arteries 3","mondo","0013463"
> "0060771","dextro-looped transposition of the great arteries 1","icd10cm","Q20.3"
> "0060771","dextro-looped transposition of the great arteries 1","mondo","0012128"
> "0060770","dextro-looped transposition of the great arteries","icd10cm","Q20.3"
> "0060770","dextro-looped transposition of the great arteries","mondo","0019443"
> "0060777","congenital secretory sodium diarrhea 8","icd10cm","P78.3"
> "0060777","congenital secretory sodium diarrhea 8","mondo","0014808"
> "0060776","congenital diarrhea 5 with tufting enteropathy","icd10cm","P78.3"
> "0060776","congenital diarrhea 5 with tufting enteropathy","mondo","0013184"
> "0060775","microvillus inclusion disease","icd10cm","P78.3"
> "0060775","microvillus inclusion disease","mesh","C537470"
> "0060775","microvillus inclusion disease","mondo","0009635"
> "0060774","congenital diarrhea","mondo","0000824"
> "5768","Nager acrofacial dysostosis","umls","C1332140"
> "5768","Nager acrofacial dysostosis","mondo","0007943"
> "5769","verruciform xanthoma of skin","umls","C0346054"
> "5769","verruciform xanthoma of skin","mondo","0003640"
> "5766","pulmonary sclerosing hemangioma","mesh","D047868"
> "5766","pulmonary sclerosing hemangioma","umls","C1334455"
> "5766","pulmonary sclerosing hemangioma","mondo","0006280"
> "5767","hilar lung neoplasm","umls","C1290358"
> "5767","hilar lung neoplasm","mondo","0003639"
> "5764","lung meningioma","umls","C1334450"
> "5764","lung meningioma","umls","C1335488"
> "5764","lung meningioma","mondo","0003638"
> "0111254","glutaric acidemia I","mesh","C536833"
> "5763","lung clear cell-sugar-tumor","umls","C1333065"
> "5763","lung clear cell-sugar-tumor","mondo","0003637"
> "5760","sebaceous breast carcinoma","umls","C1519207"
> "5760","sebaceous breast carcinoma","mondo","0003635"
> "5761","vulvar sebaceous carcinoma","umls","C1520094"
> "5761","vulvar sebaceous carcinoma","mondo","0003636"
> "1627","intraductal papilloma","mesh","D018300"
> "1627","intraductal papilloma","umls","C0206713"
> "1627","intraductal papilloma","mondo","0002060"
> "0111358","Floating-Harbor syndrome","mesh","C537062"
> "0111358","Floating-Harbor syndrome","umls","C0729582"
> "0111065","distal spinal muscular atrophy 2","mesh","C535715"
> "0111065","distal spinal muscular atrophy 2","umls","C1854023"
> "0111065","distal spinal muscular atrophy 2","mondo","0011585"
> "76","stomach disease","mesh","D013272"
> "76","stomach disease","umls","C0038354"
> "76","stomach disease","mondo","0004298"
> "12514","retinal perforation","mesh","D012167"
> "12514","retinal perforation","umls","C0035321"
> "12514","retinal perforation","mondo","0001539"
> "0111060","Ambras type hypertrichosis universalis congenita","icd10cm","Q84.2"
> "0111060","Ambras type hypertrichosis universalis congenita","mesh","C536605"
> "0111060","Ambras type hypertrichosis universalis congenita","mondo","0007787"
> "12510","retinal ischemia","icd10cm","H35.82"
> "12510","retinal ischemia","icd9cm","362.84"
> "12510","retinal ischemia","umls","C0162291"
> "12510","retinal ischemia","mondo","0001538"
> "75","lymphatic system disease","mesh","D008206"
> "75","lymphatic system disease","umls","C0024228"
> "75","lymphatic system disease","mondo","0005833"
> "7427","anthrax disease","icd10cm","A22"
> "7427","anthrax disease","icd10cm","A22.9"
> "7427","anthrax disease","icd9cm","022"
> "7427","anthrax disease","icd9cm","022.9"
> "7427","anthrax disease","mesh","D000881"
> "7427","anthrax disease","umls","C0003175"
> "7427","anthrax disease","mondo","0005119"
> "7426","cutaneous anthrax","icd10cm","A22.0"
> "7426","cutaneous anthrax","icd9cm","022.0"
> "7426","cutaneous anthrax","mesh","C531621"
> "7426","cutaneous anthrax","umls","C0003177"
> "7426","cutaneous anthrax","mondo","0004215"
> "0111359","large congenital melanocytic nevus","umls","C1318558"
> "0111359","large congenital melanocytic nevus","umls","C1842036"
> "2251","hypertrophic elongation of cervix","icd10cm","N88.4"
> "2251","hypertrophic elongation of cervix","icd9cm","622.6"
> "2251","hypertrophic elongation of cervix","umls","C0020561"
> "2251","hypertrophic elongation of cervix","mondo","0002255"
> "7429","childhood brain germinoma","umls","C1332948"
> "7429","childhood brain germinoma","mondo","0004217"
> "7428","pineal region germinoma","umls","C0854912"
> "7428","pineal region germinoma","mondo","0004216"
> "6603","Kummell's disease","icd10cm","M48.3"
> "6603","Kummell's disease","icd9cm","721.7"
> "6603","Kummell's disease","umls","C0152088"
> "6603","Kummell's disease","mondo","0003940"
> "6605","classic variant of chromophobe renal cell carcinoma","umls","C1333062"
> "6605","classic variant of chromophobe renal cell carcinoma","mondo","0003941"
> "6606","eosinophilic variant of chromophobe renal cell carcinoma","umls","C1333405"
> "6606","eosinophilic variant of chromophobe renal cell carcinoma","mondo","0003942"
> "6608","endobronchial leiomyoma","umls","C1333386"
> "6608","endobronchial leiomyoma","mondo","0003944"
> "12638","hypertrophic pyloric stenosis","icd10cm","Q40.0"
> "12638","hypertrophic pyloric stenosis","icd9cm","750.5"
> "12638","hypertrophic pyloric stenosis","mesh","D046248"
> "12638","hypertrophic pyloric stenosis","umls","C0700639"
> "12638","hypertrophic pyloric stenosis","mondo","0001560"
> "6438","malignant choroid melanoma","umls","C0346388"
> "6438","malignant choroid melanoma","mondo","0003878"
> "10854","salivary gland disease","icd9cm","527.8"
> "10854","salivary gland disease","umls","C0029773"
> "10854","salivary gland disease","mondo","0001142"
> "10852","middle ear cholesterol granuloma","icd9cm","385.82"
> "10852","middle ear cholesterol granuloma","umls","C0155492"
> "10852","middle ear cholesterol granuloma","mondo","0001141"
> "0080285","early infantile epileptic encephalopathy 58","mondo","0033367"
> "0080284","early infantile epileptic encephalopathy 57","mondo","0033366"
> "0080287","spinocerebellar ataxia 45","mondo","0033480"
> "0080286","spinocerebellar ataxia 44","mondo","0033479"
> "0080281","schizophrenia 19","mondo","0033312"
> "0080280","gingival fibromatosis 5","mondo","0033493"
> "0080283","early infantile epileptic encephalopathy 55","mondo","0033364"
> "0080282","early infantile epileptic encephalopathy 56","mondo","0033365"
> "12185","otosclerosis","icd10cm","H80.8"
> "12185","otosclerosis","icd10cm","H80.80"
> "12185","otosclerosis","icd9cm","387.8"
> "12185","otosclerosis","mesh","D010040"
> "12185","otosclerosis","umls","C0029696"
> "12185","otosclerosis","mondo","0005349"
> "0080289","orofaciodigital syndrome XVII","mondo","0033375"
> "0080288","spinocerebellar ataxia 46","mondo","0033481"
> "2352","hemochromatosis","icd10cm","E83.11"
> "2352","hemochromatosis","icd10cm","E83.110"
> "2352","hemochromatosis","icd10cm","E83.119"
> "2352","hemochromatosis","mesh","D006432"
> "2352","hemochromatosis","umls","C0018995"
> "2352","hemochromatosis","mondo","0006507"
> "2351","iron metabolism disease","icd10cm","E83.1"
> "2351","iron metabolism disease","icd10cm","E83.10"
> "2351","iron metabolism disease","icd9cm","275.0"
> "2351","iron metabolism disease","mesh","D019189"
> "2351","iron metabolism disease","umls","C0012715"
> "2351","iron metabolism disease","mondo","0002279"
> "0080001","bone disease","icd10cm","M89.9"
> "0080001","bone disease","mesh","D001847"
> "0080001","bone disease","umls","C0005940"
> "0080001","bone disease","mondo","0005381"
> "2354","myelophthisic anemia","icd10cm","D61.82"
> "2354","myelophthisic anemia","mesh","D000750"
> "2354","myelophthisic anemia","umls","C0002890"
> "2354","myelophthisic anemia","mondo","0005868"
> "2355","anemia","icd10cm","D64.9"
> "2355","anemia","icd9cm","285.9"
> "2355","anemia","mesh","D000740"
> "2355","anemia","umls","C0002871"
> "2355","anemia","mondo","0002280"
> "0050542","Charcot-Marie-Tooth disease type X","mondo","0018994"
> "0050541","Charcot-Marie-Tooth disease type 4","mondo","0018995"
> "0050540","Charcot-Marie-Tooth disease type 3","mondo","0007790"
> "0050547","familial medullary thyroid carcinoma","mondo","0007958"
> "0050546","congenital adrenal insufficiency","mondo","0013400"
> "0050545","visceral heterotaxy","mondo","0018677"
> "0050012","chikungunya","mondo","0017941"
> "0050548","hereditary sensory neuropathy","mondo","0015364"
> "1894","noninfectious dermatoses of eyelid","icd10cm","H01.1"
> "1894","noninfectious dermatoses of eyelid","icd9cm","373.3"
> "1894","noninfectious dermatoses of eyelid","umls","C0155176"
> "1894","noninfectious dermatoses of eyelid","mondo","0002137"
> "1896","sigmoid neoplasm","mesh","D012811"
> "1896","sigmoid neoplasm","umls","C0037073"
> "1896","sigmoid neoplasm","mondo","0006971"
> "1897","sigmoid disease","mesh","D012810"
> "1897","sigmoid disease","umls","C0037072"
> "1897","sigmoid disease","mondo","0002139"
> "3733","theileriasis","mesh","D013801"
> "3733","theileriasis","umls","C0039753"
> "3733","theileriasis","mondo","0005978"
> "1891","optic nerve disease","mesh","D009901"
> "1891","optic nerve disease","umls","C0029132"
> "1891","optic nerve disease","mondo","0002135"
> "1893","eczematous dermatitis of eyelid","icd10cm","H01.13"
> "1893","eczematous dermatitis of eyelid","icd9cm","373.31"
> "1893","eczematous dermatitis of eyelid","umls","C0155177"
> "1893","eczematous dermatitis of eyelid","mondo","0002136"
> "4923","thymus adenocarcinoma","umls","C1336743"
> "4923","thymus adenocarcinoma","mondo","0003209"
> "4922","breast secretory carcinoma","mesh","C537535"
> "4922","breast secretory carcinoma","umls","C0334371"
> "4922","breast secretory carcinoma","mondo","0003208"
> "4921","eccrine sweat gland cancer","umls","C1334577"
> "4921","eccrine sweat gland cancer","mondo","0005506"
> "4920","eccrine adenocarcinoma","umls","C1266066"
> "4920","eccrine adenocarcinoma","mondo","0024240"
> "4927","Klatskin's tumor","mesh","D018285"
> "4927","Klatskin's tumor","umls","C0206702"
> "4927","Klatskin's tumor","mondo","0003345"
> "4926","bronchiolo-alveolar adenocarcinoma","mesh","D002282"
> "4926","bronchiolo-alveolar adenocarcinoma","umls","C0007120"
> "4926","bronchiolo-alveolar adenocarcinoma","mondo","0004991"
> "4697","perineurioma","mesh","D018317"
> "4697","perineurioma","umls","C0751691"
> "4697","perineurioma","umls","C1370657"
> "4697","perineurioma","mondo","0019404"
> "4696","intraneural perineurioma","umls","C1370658"
> "4696","intraneural perineurioma","mondo","0015032"
> "4699","epicardium cancer","umls","C0346610"
> "4699","epicardium cancer","umls","C1290403"
> "4699","epicardium cancer","mondo","0003104"
> "4698","nerve root neoplasm","umls","C1334946"
> "4698","nerve root neoplasm","mondo","0003103"
> "4929","tubular adenocarcinoma","mesh","D000230"
> "4929","tubular adenocarcinoma","umls","C0205645"
> "4929","tubular adenocarcinoma","mondo","0005606"
> "4928","intrahepatic cholangiocarcinoma","icd10cm","C22.1"
> "4928","intrahepatic cholangiocarcinoma","mesh","D018281"
> "4928","intrahepatic cholangiocarcinoma","umls","C0345905"
> "4928","intrahepatic cholangiocarcinoma","mondo","0003210"
> "2139","paraurethral gland neoplasm","umls","C0341766"
> "2139","paraurethral gland neoplasm","mondo","0002219"
> "11726","Emery-Dreifuss muscular dystrophy","mesh","D020389"
> "11726","Emery-Dreifuss muscular dystrophy","umls","C0410189"
> "11726","Emery-Dreifuss muscular dystrophy","mondo","0016830"
> "11727","facioscapulohumeral muscular dystrophy","icd10cm","G71.0"
> "11727","facioscapulohumeral muscular dystrophy","mesh","D020391"
> "11727","facioscapulohumeral muscular dystrophy","umls","C0238288"
> "11727","facioscapulohumeral muscular dystrophy","mondo","0001347"
> "11724","limb-girdle muscular dystrophy","icd10cm","G71.0"
> "11724","limb-girdle muscular dystrophy","mesh","D049288"
> "11724","limb-girdle muscular dystrophy","umls","C0686353"
> "11724","limb-girdle muscular dystrophy","mondo","0016971"
> "11725","Cornelia de Lange syndrome","icd10cm","Q87.1"
> "11725","Cornelia de Lange syndrome","mesh","D003635"
> "11725","Cornelia de Lange syndrome","umls","C0270972"
> "11725","Cornelia de Lange syndrome","mondo","0016033"
> "11722","myotonic dystrophy type 1","icd10cm","G71.11"
> "11722","myotonic dystrophy type 1","icd9cm","359.21"
> "11722","myotonic dystrophy type 1","mesh","D009223"
> "11722","myotonic dystrophy type 1","umls","C0027126"
> "11722","myotonic dystrophy type 1","mondo","0008056"
> "11723","Duchenne muscular dystrophy","mesh","D020388"
> "11723","Duchenne muscular dystrophy","umls","C0013264"
> "11723","Duchenne muscular dystrophy","mondo","0010679"
> "11720","distal myopathy","icd10cm","G71.0"
> "11720","distal myopathy","mesh","D049310"
> "11720","distal myopathy","umls","C0751336"
> "11720","distal myopathy","mondo","0018949"
> "11721","glycogen storage disease VII","icd10cm","E74.09"
> "11721","glycogen storage disease VII","mesh","D006014"
> "11721","glycogen storage disease VII","umls","C0017926"
> "11721","glycogen storage disease VII","mondo","0009295"
> "11729","Lyme disease","icd10cm","A69.2"
> "11729","Lyme disease","icd10cm","A69.20"
> "11729","Lyme disease","icd9cm","088.81"
> "11729","Lyme disease","mesh","D008193"
> "11729","Lyme disease","mesh","D020852"
> "11729","Lyme disease","umls","C0024198"
> "11729","Lyme disease","umls","C0752235"
> "11729","Lyme disease","mondo","0019632"
> "5160","arteriosclerosis obliterans","mesh","D001162"
> "5160","arteriosclerosis obliterans","umls","C0003851"
> "5160","arteriosclerosis obliterans","mondo","0006659"
> "5162","arteriolosclerosis","icd10cm","I70"
> "5162","arteriolosclerosis","mesh","D050379"
> "5162","arteriolosclerosis","umls","C0878486"
> "5162","arteriolosclerosis","mondo","0006658"
> "5165","uterine corpus sarcoma","umls","C0338113"
> "5165","uterine corpus sarcoma","mondo","0005210"
> "5166","endometrial stromal tumor","mesh","D036821"
> "5166","endometrial stromal tumor","umls","C0334695"
> "5166","endometrial stromal tumor","mondo","0003311"
> "14000","rubeosis iridis","icd10cm","H21.1"
> "14000","rubeosis iridis","icd9cm","364.42"
> "14000","rubeosis iridis","umls","C0154916"
> "14000","rubeosis iridis","mondo","0001855"
> "5169","ovarian endometrioid stromal sarcoma","umls","C4288544"
> "5169","ovarian endometrioid stromal sarcoma","mondo","0003312"
> "14004","thoracic aortic aneurysm","mesh","D017545"
> "14004","thoracic aortic aneurysm","umls","C0162872"
> "14004","thoracic aortic aneurysm","mondo","0005396"
> "14006","splenic artery aneurysm","icd9cm","442.83"
> "14006","splenic artery aneurysm","umls","C0155747"
> "14006","splenic artery aneurysm","mondo","0001856"
> "9698","gonococcal endophthalmia","icd10cm","A54.39"
> "9698","gonococcal endophthalmia","icd9cm","098.42"
> "9698","gonococcal endophthalmia","umls","C0153213"
> "9698","gonococcal endophthalmia","mondo","0004853"
> "9699","ophthalmia neonatorum","icd10cm","P39.1"
> "9699","ophthalmia neonatorum","icd9cm","771.6"
> "9699","ophthalmia neonatorum","umls","C0027611"
> "9699","ophthalmia neonatorum","umls","C0029076"
> "9699","ophthalmia neonatorum","mondo","0004854"
> "9697","gonococcal keratitis","icd10cm","A54.33"
> "9697","gonococcal keratitis","icd9cm","098.43"
> "9697","gonococcal keratitis","umls","C0153214"
> "9697","gonococcal keratitis","mondo","0004852"
> "9694","toxic myocarditis","icd9cm","422.93"
> "9694","toxic myocarditis","umls","C0155691"
> "9694","toxic myocarditis","mondo","0004851"
> "668","myositis ossificans","mesh","D009221"
> "668","myositis ossificans","umls","C0027122"
> "668","myositis ossificans","mondo","0003964"
> "10600","chronic tic disorder","icd10cm","F95.1"
> "10600","chronic tic disorder","icd9cm","307.22"
> "10600","chronic tic disorder","mesh","D013981"
> "10600","chronic tic disorder","umls","C0008701"
> "10600","chronic tic disorder","mondo","0001074"
> "13649","polyneuropathy in collagen vascular disease","icd9cm","357.1"
> "13649","polyneuropathy in collagen vascular disease","umls","C0154759"
> "13649","polyneuropathy in collagen vascular disease","mondo","0001765"
> "10606","blind loop syndrome","icd10cm","K90.2"
> "10606","blind loop syndrome","icd9cm","579.2"
> "10606","blind loop syndrome","mesh","D001765"
> "10606","blind loop syndrome","umls","C0005750"
> "10606","blind loop syndrome","mondo","0005673"
> "10607","tropical sprue","icd10cm","K90.1"
> "10607","tropical sprue","icd9cm","579.1"
> "10607","tropical sprue","mesh","D013182"
> "10607","tropical sprue","umls","C0038054"
> "10607","tropical sprue","mondo","0001078"
> "1799","islet cell tumor","icd10cm","C25.4"
> "1799","islet cell tumor","icd10cm","D13.7"
> "1799","islet cell tumor","mesh","D007516"
> "1799","islet cell tumor","umls","C0242363"
> "1799","islet cell tumor","umls","C0496784"
> "1799","islet cell tumor","mondo","0005815"
> "1260","parametritis","mesh","D010249"
> "1260","parametritis","umls","C0030455"
> "1260","parametritis","mondo","0006887"
> "10604","lactose intolerance","icd10cm","E73"
> "10604","lactose intolerance","icd10cm","E73.9"
> "10604","lactose intolerance","mesh","D007787"
> "10604","lactose intolerance","umls","C0022951"
> "10604","lactose intolerance","mondo","0009116"
> "1793","pancreatic cancer","kegg","05212"
> "1793","pancreatic cancer","icd10cm","C25.0"
> "1793","pancreatic cancer","icd10cm","C25.1"
> "1793","pancreatic cancer","icd10cm","C25.2"
> "1793","pancreatic cancer","icd9cm","157.0"
> "1793","pancreatic cancer","icd9cm","157.1"
> "1793","pancreatic cancer","icd9cm","157.2"
> "1793","pancreatic cancer","icd9cm","157.8"
> "1793","pancreatic cancer","mesh","D010190"
> "1793","pancreatic cancer","umls","C0030297"
> "1793","pancreatic cancer","umls","C0153458"
> "1793","pancreatic cancer","umls","C0153459"
> "1793","pancreatic cancer","umls","C0153460"
> "1793","pancreatic cancer","umls","C0153463"
> "1793","pancreatic cancer","mondo","0009831"
> "8259","bulbomembranous urethral cancer","umls","C1511339"
> "8259","bulbomembranous urethral cancer","mondo","0004516"
> "1791","peritoneal carcinoma","umls","C1514428"
> "1791","peritoneal carcinoma","mondo","0002113"
> "1790","malignant mesothelioma","mesh","C562839"
> "1790","malignant mesothelioma","umls","C0278752"
> "1790","malignant mesothelioma","umls","C0345967"
> "1790","malignant mesothelioma","umls","C0392400"
> "1790","malignant mesothelioma","umls","C1332338"
> "1790","malignant mesothelioma","mondo","0006292"
> "1796","pancreas sarcoma","umls","C1096346"
> "1796","pancreas sarcoma","mondo","0002117"
> "1795","tumor of exocrine pancreas","umls","C0345920"
> "1795","tumor of exocrine pancreas","umls","C0346648"
> "1795","tumor of exocrine pancreas","mondo","0002116"
> "2073","perinatal intestinal perforation","icd10cm","P78.0"
> "2073","perinatal intestinal perforation","icd9cm","777.6"
> "2073","perinatal intestinal perforation","umls","C0159006"
> "2073","perinatal intestinal perforation","mondo","0002196"
> "6848","adult vagina botryoid rhabdomyosarcoma","umls","C1515893"
> "6848","adult vagina botryoid rhabdomyosarcoma","mondo","0004013"
> "6841","flat ductal epithelial atypia","umls","C1333620"
> "6841","flat ductal epithelial atypia","mondo","0004008"
> "6846","familial melanoma","umls","C1512419"
> "6846","familial melanoma","mondo","0018961"
> "6847","adult botryoid rhabdomyosarcoma","umls","C1332185"
> "6847","adult botryoid rhabdomyosarcoma","mondo","0004012"
> "6844","kidney pelvis sarcomatoid transitional cell carcinoma","umls","C1335752"
> "6844","kidney pelvis sarcomatoid transitional cell carcinoma","mondo","0004009"
> "6845","infiltrating ureter transitional cell carcinoma","umls","C1512750"
> "6845","infiltrating ureter transitional cell carcinoma","mondo","0020658"
> "10609","rickets","icd10cm","E55.0"
> "10609","rickets","icd9cm","268.0"
> "10609","rickets","mesh","D012279"
> "10609","rickets","umls","C0035579"
> "10609","rickets","umls","C0221468"
> "10609","rickets","mondo","0005520"
> "2076","vulvar glandular tumor","umls","C1520082"
> "2076","vulvar glandular tumor","mondo","0002198"
> "0110298","autosomal recessive limb-girdle muscular dystrophy type 2N","icd10cm","G71.0"
> "0110298","autosomal recessive limb-girdle muscular dystrophy type 2N","mondo","0013162"
> "0110299","autosomal recessive limb-girdle muscular dystrophy type 2I","icd10cm","G71.0"
> "0110299","autosomal recessive limb-girdle muscular dystrophy type 2I","mondo","0011787"
> "0110294","autosomal recessive limb-girdle muscular dystrophy type 2T","icd10cm","G71.0"
> "0110294","autosomal recessive limb-girdle muscular dystrophy type 2T","mondo","0014142"
> "0110295","autosomal recessive limb-girdle muscular dystrophy type 2U","icd10cm","G71.0"
> "0110295","autosomal recessive limb-girdle muscular dystrophy type 2U","mondo","0014474"
> "0110296","autosomal recessive limb-girdle muscular dystrophy type 2M","icd10cm","G71.0"
> "0110296","autosomal recessive limb-girdle muscular dystrophy type 2M","mondo","0012699"
> "0110297","autosomal recessive limb-girdle muscular dystrophy type 2K","icd10cm","G71.0"
> "0110297","autosomal recessive limb-girdle muscular dystrophy type 2K","mondo","0012248"
> "0110290","autosomal recessive limb-girdle muscular dystrophy type 2X","mondo","0014782"
> "0110291","Leber congenital amaurosis 10","icd10cm","H35.5"
> "0110291","Leber congenital amaurosis 10","mondo","0012723"
> "0110292","autosomal recessive limb-girdle muscular dystrophy type 2O","icd10cm","G71.0"
> "0110292","autosomal recessive limb-girdle muscular dystrophy type 2O","mondo","0013161"
> "0110293","autosomal recessive limb-girdle muscular dystrophy type 2P","icd10cm","G71.0"
> "0110293","autosomal recessive limb-girdle muscular dystrophy type 2P","mondo","0013440"
> "8233","inflammatory liposarcoma","umls","C1370890"
> "8233","inflammatory liposarcoma","mondo","0004510"
> "8230","intrahepatic biliary papillomatosis","umls","C1334258"
> "8230","intrahepatic biliary papillomatosis","mondo","0004509"
> "6594","bladder colonic type adenocarcinoma","umls","C1511188"
> "6594","bladder colonic type adenocarcinoma","mondo","0003938"
> "6595","gastric tubular adenocarcinoma","umls","C1333791"
> "6595","gastric tubular adenocarcinoma","mondo","0006035"
> "8239","lower clivus meningioma","umls","C1334434"
> "8239","lower clivus meningioma","mondo","0004511"
> "0060540","Hermansky-Pudlak syndrome 2","mondo","0011997"
> "0060541","Hermansky-Pudlak syndrome 3","mondo","0013555"
> "0060542","Hermansky-Pudlak syndrome 4","mondo","0013556"
> "7639","malignant granular cell skin tumor","umls","C1334575"
> "7639","malignant granular cell skin tumor","mondo","0004314"
> "0060544","Hermansky-Pudlak syndrome 6","mondo","0013558"
> "0060545","Hermansky-Pudlak syndrome 7","mondo","0013559"
> "0060546","Hermansky-Pudlak syndrome 8","mondo","0013560"
> "0060547","Hermansky-Pudlak syndrome 9","mondo","0013606"
> "0060548","luminal breast carcinoma","mondo","0004990"
> "0060549","Barber-Say syndrome","mesh","C537908"
> "0060549","Barber-Say syndrome","umls","C1319466"
> "0060549","Barber-Say syndrome","mondo","0008853"
> "7631","adult ependymoblastoma","umls","C0281330"
> "7631","adult ependymoblastoma","mondo","0004310"
> "7634","suprasellar meningioma","umls","C1336535"
> "7634","suprasellar meningioma","mondo","0004312"
> "7635","Gasserian ganglion meningioma","umls","C1333760"
> "7635","Gasserian ganglion meningioma","mondo","0004313"
> "0111537","paroxysmal extreme pain disorder","mesh","C563475"
> "0111537","paroxysmal extreme pain disorder","umls","C1833661"
> "0111532","osteoglophonic dysplasia","mesh","C536050"
> "0111532","osteoglophonic dysplasia","umls","C0432283"
> "0111533","gnathodiaphyseal dysplasia","mesh","C536039"
> "0111533","gnathodiaphyseal dysplasia","umls","C1833736"
> "9843","monofixation syndrome","icd10cm","H50.42"
> "9843","monofixation syndrome","icd9cm","378.34"
> "9843","monofixation syndrome","umls","C0339611"
> "9843","monofixation syndrome","mondo","0004899"
> "9842","total circumpapillary dystrophy of choroid","icd9cm","363.52"
> "9842","total circumpapillary dystrophy of choroid","umls","C0154896"
> "9842","total circumpapillary dystrophy of choroid","mondo","0004898"
> "9841","hypotropia","icd9cm","378.32"
> "9841","hypotropia","umls","C0152208"
> "9841","hypotropia","mondo","0004897"
> "9840","esotropia","icd10cm","H50.0"
> "9840","esotropia","icd10cm","H50.00"
> "9840","esotropia","icd9cm","378.0"
> "9840","esotropia","icd9cm","378.00"
> "9840","esotropia","mesh","D004948"
> "9840","esotropia","umls","C0014877"
> "9840","esotropia","mondo","0004896"
> "9847","peripheral vertigo","icd10cm","H81.3"
> "9847","peripheral vertigo","icd10cm","H81.39"
> "9847","peripheral vertigo","icd10cm","H81.399"
> "9847","peripheral vertigo","icd9cm","386.1"
> "9847","peripheral vertigo","icd9cm","386.19"
> "9847","peripheral vertigo","umls","C0029706"
> "9847","peripheral vertigo","mondo","0004900"
> "9849","Meniere's disease","icd10cm","H81.0"
> "9849","Meniere's disease","icd10cm","H81.09"
> "9849","Meniere's disease","icd9cm","386.0"
> "9849","Meniere's disease","icd9cm","386.00"
> "9849","Meniere's disease","mesh","D008575"
> "9849","Meniere's disease","umls","C0025281"
> "9849","Meniere's disease","mondo","0007972"
> "9848","endolymphatic hydrops","icd10cm","H81.0"
> "9848","endolymphatic hydrops","mesh","D018159"
> "9848","endolymphatic hydrops","umls","C0206586"
> "9848","endolymphatic hydrops","mondo","0006744"
> "1241","luxation of globe","icd10cm","H44.82"
> "1241","luxation of globe","icd9cm","360.81"
> "1241","luxation of globe","umls","C0154806"
> "1241","luxation of globe","mondo","0001523"
> "3093","nervous system cancer","icd9cm","192"
> "3093","nervous system cancer","icd9cm","192.9"
> "3093","nervous system cancer","mesh","D009380"
> "3093","nervous system cancer","umls","C0027665"
> "3093","nervous system cancer","umls","C0153643"
> "3093","nervous system cancer","umls","C1334956"
> "3093","nervous system cancer","mondo","0005872"
> "643","progressive multifocal leukoencephalopathy","icd10cm","A81.2"
> "643","progressive multifocal leukoencephalopathy","icd9cm","046.3"
> "643","progressive multifocal leukoencephalopathy","mesh","D007968"
> "643","progressive multifocal leukoencephalopathy","umls","C0023524"
> "643","progressive multifocal leukoencephalopathy","mondo","0016318"
> "1242","globe disease","icd10cm","H44.39"
> "1242","globe disease","icd9cm","360.29"
> "1242","globe disease","umls","C0154780"
> "1242","globe disease","mondo","0001524"
> "3096","stenosis of lacrimal sac","icd10cm","H04.57"
> "3096","stenosis of lacrimal sac","icd10cm","H04.579"
> "3096","stenosis of lacrimal sac","icd9cm","375.54"
> "3096","stenosis of lacrimal sac","umls","C0155246"
> "3096","stenosis of lacrimal sac","mondo","0002511"
> "1532","pleural disease","mesh","D010995"
> "1532","pleural disease","umls","C0032226"
> "1532","pleural disease","mondo","0002037"
> "1247","blood coagulation disease","icd10cm","D68.9"
> "1247","blood coagulation disease","icd9cm","286"
> "1247","blood coagulation disease","mesh","D001778"
> "1247","blood coagulation disease","umls","C0005779"
> "1247","blood coagulation disease","mondo","0001531"
> "646","viral encephalitis","mesh","D004671"
> "646","viral encephalitis","umls","C0014055"
> "646","viral encephalitis","mondo","0006009"
> "649","prion disease","kegg","05020"
> "649","prion disease","icd10cm","A81.9"
> "649","prion disease","mesh","D017096"
> "649","prion disease","umls","C0162534"
> "649","prion disease","mondo","0005429"
> "648","kuru","icd10cm","A81.81"
> "648","kuru","icd9cm","046.0"
> "648","kuru","mesh","D007729"
> "648","kuru","umls","C0022802"
> "648","kuru","mondo","0006825"
> "3098","small cell sarcoma","mesh","D018228"
> "3098","small cell sarcoma","umls","C0206652"
> "3098","small cell sarcoma","mondo","0006974"
> "4109","tick infestation","mesh","D013984"
> "4109","tick infestation","umls","C0040196"
> "4109","tick infestation","mondo","0005980"
> "9312","chronic ethmoiditis","icd10cm","J32.2"
> "9312","chronic ethmoiditis","icd9cm","473.2"
> "9312","chronic ethmoiditis","umls","C0008681"
> "9312","chronic ethmoiditis","mondo","0004757"
> "3892","insulinoma","mesh","D007340"
> "3892","insulinoma","mesh","D007516"
> "3892","insulinoma","umls","C0021670"
> "3892","insulinoma","umls","C0022134"
> "3892","insulinoma","mondo","0024677"
> "3893","hidrocystoma","mesh","D018251"
> "3893","hidrocystoma","umls","C0206672"
> "3893","hidrocystoma","mondo","0006787"
> "3890","acute intermittent porphyria","mesh","D017118"
> "3890","acute intermittent porphyria","umls","C0162565"
> "3890","acute intermittent porphyria","mondo","0008294"
> "3891","placental insufficiency","mesh","D010927"
> "3891","placental insufficiency","umls","C0032051"
> "3891","placental insufficiency","mondo","0005919"
> "3896","hidradenoma","mesh","D006607"
> "3896","hidradenoma","umls","C0019522"
> "3896","hidradenoma","mondo","0002805"
> "3895","apocrine adenoma","umls","C0334345"
> "3895","apocrine adenoma","mondo","0002804"
> "0110489","autosomal recessive nonsyndromic deafness 30","icd10cm","H90.3"
> "0110489","autosomal recessive nonsyndromic deafness 30","mondo","0011774"
> "14456","Brucella melitensis brucellosis","icd10cm","A23.0"
> "14456","Brucella melitensis brucellosis","icd9cm","023.0"
> "14456","Brucella melitensis brucellosis","umls","C0302362"
> "14456","Brucella melitensis brucellosis","mondo","0001972"
> "8955","sideroblastic anemia","icd10cm","D64.3"
> "8955","sideroblastic anemia","icd9cm","285.0"
> "8955","sideroblastic anemia","mesh","D000756"
> "8955","sideroblastic anemia","umls","C0002896"
> "8955","sideroblastic anemia","mondo","0015194"
> "5957","bladder urachal squamous cell carcinoma","umls","C1511206"
> "5957","bladder urachal squamous cell carcinoma","mondo","0003714"
> "5958","bladder urachal carcinoma","umls","C1511205"
> "5958","bladder urachal carcinoma","mondo","0003715"
> "13417","alexia","icd9cm","315.01"
> "13417","alexia","mesh","D004410"
> "13417","alexia","mesh","D004411"
> "13417","alexia","umls","C0002018"
> "13417","alexia","umls","C0013388"
> "13417","alexia","mondo","0001712"
> "1023","borderline leprosy","icd10cm","A30.3"
> "1023","borderline leprosy","icd9cm","030.3"
> "1023","borderline leprosy","mesh","D015439"
> "1023","borderline leprosy","umls","C0023346"
> "1023","borderline leprosy","mondo","0005125"
> "238","pupil disease","mesh","D011681"
> "238","pupil disease","umls","C0034124"
> "238","pupil disease","mondo","0002285"
> "0090042","torsion dystonia 17","icd10cm","G24.1"
> "0090042","torsion dystonia 17","mondo","0012895"
> "0090043","dystonia 5","icd10cm","G24.1"
> "0090043","dystonia 5","mondo","0007495"
> "0090040","torsion dystonia 7","mondo","0011200"
> "0090041","torsion dystonia 4","icd10cm","G24.1"
> "0090041","torsion dystonia 4","mondo","0007493"
> "0090046","dystonia 21","icd10cm","G24.1"
> "0090046","dystonia 21","mondo","0013813"
> "0090047","paroxysmal nonkinesigenic dyskinesia 2","icd10cm","G24.8"
> "0090047","paroxysmal nonkinesigenic dyskinesia 2","mondo","0012629"
> "0090044","dystonia 9","icd10cm","G24.8"
> "0090044","dystonia 9","mondo","0010983"
> "0090045","childhood onset GLUT1 deficiency syndrome 2","icd10cm","G24.8"
> "0090045","childhood onset GLUT1 deficiency syndrome 2","mondo","0012805"
> "0090048","dystonia 16","icd10cm","G24.1"
> "0090048","dystonia 16","mondo","0012789"
> "0090049","paroxysmal nonkinesigenic dyskinesia 1","icd10cm","G24.8"
> "0090049","paroxysmal nonkinesigenic dyskinesia 1","mondo","0007326"
> "0110904","inflammatory bowel disease 8","mondo","0011699"
> "0110905","inflammatory bowel disease 22","mondo","0012886"
> "0110906","inflammatory bowel disease 21","mondo","0012875"
> "0110907","inflammatory bowel disease 6","mondo","0011700"
> "0110900","inflammatory bowel disease 2","mondo","0011087"
> "0110901","inflammatory bowel disease 26","mondo","0012973"
> "0110902","inflammatory bowel disease 27","mondo","0013012"
> "0110903","inflammatory bowel disease 4","mondo","0011701"
> "0110908","inflammatory bowel disease 24","mondo","0012940"
> "0110909","inflammatory bowel disease 25","mondo","0012941"
> "1455","geographic tongue","icd10cm","K14.1"
> "1455","geographic tongue","icd9cm","529.1"
> "1455","geographic tongue","mesh","D005929"
> "1455","geographic tongue","umls","C0017677"
> "1455","geographic tongue","mondo","0005771"
> "14452","hypokalemic periodic paralysis","icd10cm","G72.3"
> "14452","hypokalemic periodic paralysis","mesh","D020514"
> "14452","hypokalemic periodic paralysis","umls","C0238358"
> "14452","hypokalemic periodic paralysis","mondo","0008223"
> "0110849","xeroderma pigmentosum group G","icd10cm","Q82.1"
> "0110849","xeroderma pigmentosum group G","mondo","0010216"
> "0110848","xeroderma pigmentosum group F","icd10cm","Q82.1"
> "0110848","xeroderma pigmentosum group F","mondo","0010215"
> "0110841","Usher syndrome type 3A","icd10cm","H35.5"
> "0110841","Usher syndrome type 3A","mondo","0010170"
> "0110840","Usher syndrome type 2D","icd10cm","H35.5"
> "0110840","Usher syndrome type 2D","mondo","0012662"
> "0110843","xeroderma pigmentosum group A","icd10cm","Q82.1"
> "0110843","xeroderma pigmentosum group A","mondo","0010210"
> "0110842","Usher syndrome type 3B","icd10cm","H35.5"
> "0110842","Usher syndrome type 3B","mondo","0013788"
> "0110845","xeroderma pigmentosum group D","icd10cm","Q82.1"
> "0110845","xeroderma pigmentosum group D","mondo","0010212"
> "0110844","xeroderma pigmentosum group C","icd10cm","Q82.1"
> "0110844","xeroderma pigmentosum group C","mondo","0010211"
> "0110847","xeroderma pigmentosum variant type","icd10cm","Q82.1"
> "0110847","xeroderma pigmentosum variant type","mondo","0010214"
> "0110846","xeroderma pigmentosum group E","icd10cm","Q82.1"
> "0110846","xeroderma pigmentosum group E","mondo","0010213"
> "6039","uveal melanoma","mesh","C536494"
> "6039","uveal melanoma","umls","C0220633"
> "6039","uveal melanoma","mondo","0006486"
> "6033","heart fibrosarcoma","umls","C1332844"
> "6033","heart fibrosarcoma","mondo","0003742"
> "6032","juvenile type testicular granulosa cell tumor","umls","C0334403"
> "6032","juvenile type testicular granulosa cell tumor","umls","C1515285"
> "6032","juvenile type testicular granulosa cell tumor","mondo","0003741"
> "6037","spindle cell intraocular melanoma","umls","C0279687"
> "6037","spindle cell intraocular melanoma","mondo","0003744"
> "6034","heart malignant hemangiopericytoma","umls","C1334567"
> "6034","heart malignant hemangiopericytoma","mondo","0003743"
> "9207","periodic limb movement disorder","icd10cm","G47.61"
> "9207","periodic limb movement disorder","icd9cm","327.51"
> "9207","periodic limb movement disorder","mesh","D020189"
> "9207","periodic limb movement disorder","umls","C0751774"
> "9207","periodic limb movement disorder","mondo","0005905"
> "9206","Barrett's esophagus","icd10cm","K22.7"
> "9206","Barrett's esophagus","icd10cm","K22.70"
> "9206","Barrett's esophagus","icd9cm","530.85"
> "9206","Barrett's esophagus","mesh","D001471"
> "9206","Barrett's esophagus","umls","C0004763"
> "9206","Barrett's esophagus","mondo","0013662"
> "9201","lichen planus","icd10cm","L43"
> "9201","lichen planus","icd10cm","L43.9"
> "9201","lichen planus","icd9cm","697.0"
> "9201","lichen planus","mesh","D008010"
> "9201","lichen planus","umls","C0023646"
> "9201","lichen planus","mondo","0006572"
> "2653","benign fibrous mesothelioma","mesh","D054363"
> "2653","benign fibrous mesothelioma","umls","C0334511"
> "2653","benign fibrous mesothelioma","mondo","0006674"
> "10069","subglottis neoplasm","umls","C0345746"
> "10069","subglottis neoplasm","mondo","0000933"
> "2656","breast intracanalicular fibroadenoma","umls","C0334496"
> "2656","breast intracanalicular fibroadenoma","mondo","0002377"
> "0110593","autosomal dominant nonsyndromic deafness 9","icd10cm","H90.3"
> "0110593","autosomal dominant nonsyndromic deafness 9","mondo","0011058"
> "0110592","autosomal dominant nonsyndromic deafness 70","icd10cm","H90.3"
> "0110592","autosomal dominant nonsyndromic deafness 70","mondo","0014853"
> "7388","pulmonary vein leiomyosarcoma","umls","C1335575"
> "7388","pulmonary vein leiomyosarcoma","mondo","0004206"
> "7389","pulmonary artery leiomyosarcoma","umls","C1335572"
> "7389","pulmonary artery leiomyosarcoma","mondo","0004207"
> "0110597","primary ciliary dyskinesia 22","icd10cm","Q34.8"
> "0110597","primary ciliary dyskinesia 22","mondo","0014192"
> "0110596","primary ciliary dyskinesia 21","icd10cm","Q34.8"
> "0110596","primary ciliary dyskinesia 21","mondo","0014123"
> "0110595","Stromme syndrome","icd10cm","Q87.8"
> "0110595","Stromme syndrome","mondo","0009477"
> "0110594","primary ciliary dyskinesia 1","icd10cm","Q34.8"
> "0110594","primary ciliary dyskinesia 1","mondo","0009484"
> "7380","squamous cell papilloma of skin","umls","C0345983"
> "7380","squamous cell papilloma of skin","mondo","0004204"
> "7381","lymphohistiocytoid mesothelioma","umls","C1334464"
> "7381","lymphohistiocytoid mesothelioma","mondo","0004205"
> "12375","bronchopneumonia","icd10cm","J18.0"
> "12375","bronchopneumonia","icd9cm","485"
> "12375","bronchopneumonia","mesh","D001996"
> "12375","bronchopneumonia","umls","C0006285"
> "12375","bronchopneumonia","mondo","0005682"
> "12376","juvenile spinal muscular atrophy","icd9cm","335.11"
> "12376","juvenile spinal muscular atrophy","mesh","D014897"
> "12376","juvenile spinal muscular atrophy","umls","C0152109"
> "12376","juvenile spinal muscular atrophy","umls","C0700595"
> "12376","juvenile spinal muscular atrophy","mondo","0009672"
> "12377","spinal muscular atrophy","icd10cm","G12.9"
> "12377","spinal muscular atrophy","icd9cm","335.1"
> "12377","spinal muscular atrophy","icd9cm","335.10"
> "12377","spinal muscular atrophy","mesh","D009134"
> "12377","spinal muscular atrophy","umls","C0026847"
> "12377","spinal muscular atrophy","mondo","0001516"
> "0050486","exanthem","icd10cm","R21"
> "0050486","exanthem","icd9cm","782.1"
> "0050486","exanthem","mesh","D005076"
> "0050486","exanthem","umls","C0015230"
> "0050486","exanthem","mondo","0006547"
> "0050485","sennetsu fever","mondo","0000332"
> "9060","pityriasis versicolor","icd10cm","B36.0"
> "9060","pityriasis versicolor","icd9cm","111.0"
> "9060","pityriasis versicolor","mesh","D014010"
> "9060","pityriasis versicolor","umls","C0040262"
> "9060","pityriasis versicolor","mondo","0005915"
> "9063","Ritter's disease","icd10cm","L00"
> "9063","Ritter's disease","icd9cm","695.81"
> "9063","Ritter's disease","mesh","D013206"
> "9063","Ritter's disease","umls","C0038165"
> "9063","Ritter's disease","mondo","0005948"
> "9065","leishmaniasis","icd10cm","B55"
> "9065","leishmaniasis","icd10cm","B55.9"
> "9065","leishmaniasis","icd9cm","085"
> "9065","leishmaniasis","icd9cm","085.9"
> "9065","leishmaniasis","mesh","D007896"
> "9065","leishmaniasis","umls","C0023281"
> "9065","leishmaniasis","mondo","0011989"
> "10289","prostate malignant phyllodes tumor","mesh","C549759"
> "10289","prostate malignant phyllodes tumor","umls","C1334615"
> "10289","prostate malignant phyllodes tumor","mondo","0000994"
> "10286","prostate carcinoma","kegg","05215"
> "10286","prostate carcinoma","umls","C0600139"
> "10286","prostate carcinoma","mondo","0005159"
> "10287","prostate squamous cell carcinoma","umls","C1302530"
> "10287","prostate squamous cell carcinoma","mondo","0000993"
> "10283","prostate cancer","kegg","05215"
> "10283","prostate cancer","icd10cm","C61"
> "10283","prostate cancer","icd9cm","185"
> "10283","prostate cancer","mesh","D011471"
> "10283","prostate cancer","umls","C0033578"
> "10283","prostate cancer","umls","C0376358"
> "10283","prostate cancer","mondo","0008315"
> "3565","meningioma","icd10cm","D32.9"
> "3565","meningioma","mesh","D008577"
> "3565","meningioma","mesh","D008579"
> "3565","meningioma","umls","C0025284"
> "3565","meningioma","umls","C0025286"
> "3565","meningioma","umls","C0349604"
> "3565","meningioma","umls","C1334698"
> "3565","meningioma","umls","C1336537"
> "3565","meningioma","mondo","0016642"
> "4486","malignant biphasic mesothelioma","umls","C0334515"
> "4486","malignant biphasic mesothelioma","mondo","0006109"
> "4480","achondroplasia","icd10cm","Q77.4"
> "4480","achondroplasia","mesh","D000130"
> "4480","achondroplasia","umls","C0001080"
> "4480","achondroplasia","mondo","0007037"
> "4481","allergic rhinitis","mesh","D065631"
> "4481","allergic rhinitis","umls","C0002103"
> "4481","allergic rhinitis","mondo","0011786"
> "4483","rhinitis","mesh","D012220"
> "4483","rhinitis","umls","C0035455"
> "4483","rhinitis","mondo","0003014"
> "4488","sarcomatoid mesothelioma","umls","C0334513"
> "4488","sarcomatoid mesothelioma","mondo","0006407"
> "4489","malignant epithelial mesothelioma","umls","C0862312"
> "4489","malignant epithelial mesothelioma","mondo","0005599"
> "0110337","osteogenesis imperfecta type 7","icd10cm","Q78.0"
> "0110337","osteogenesis imperfecta type 7","mondo","0012536"
> "0110336","osteogenesis imperfecta type 8","icd10cm","Q78.0"
> "0110336","osteogenesis imperfecta type 8","mondo","0012581"
> "0110335","osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures","icd10cm","Q78.0"
> "0110335","osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures","mondo","0008149"
> "0110334","osteogenesis imperfecta type 1","icd10cm","Q78.0"
> "0110334","osteogenesis imperfecta type 1","mondo","0008146"
> "2907","Goldenhar syndrome","icd10cm","Q87.0"
> "2907","Goldenhar syndrome","mesh","D006053"
> "2907","Goldenhar syndrome","umls","C0265240"
> "2907","Goldenhar syndrome","mondo","0008112"
> "709","splenic manifestation of hairy cell leukemia","icd9cm","202.47"
> "709","splenic manifestation of hairy cell leukemia","umls","C0153832"
> "709","splenic manifestation of hairy cell leukemia","umls","C1336064"
> "709","splenic manifestation of hairy cell leukemia","mondo","0004104"
> "0110331","Leber congenital amaurosis 3","icd10cm","H35.5"
> "0110331","Leber congenital amaurosis 3","mondo","0011415"
> "0110330","Leber congenital amaurosis 13","icd10cm","H35.5"
> "0110330","Leber congenital amaurosis 13","mondo","0012990"
> "705","Leber hereditary optic neuropathy","icd10cm","H47.22"
> "705","Leber hereditary optic neuropathy","mesh","D029242"
> "705","Leber hereditary optic neuropathy","umls","C0917796"
> "705","Leber hereditary optic neuropathy","mondo","0010788"
> "706","mature B-cell neoplasm","umls","C1334633"
> "706","mature B-cell neoplasm","mondo","0004949"
> "707","B-cell lymphoma","mesh","D016393"
> "707","B-cell lymphoma","umls","C0079731"
> "707","B-cell lymphoma","mondo","0004095"
> "700","mitochondrial metabolism disease","icd10cm","E88.4"
> "700","mitochondrial metabolism disease","mesh","D028361"
> "700","mitochondrial metabolism disease","umls","C0751651"
> "700","mitochondrial metabolism disease","mondo","0004069"
> "701","dentin dysplasia","icd10cm","K00.5"
> "701","dentin dysplasia","mesh","D003805"
> "701","dentin dysplasia","umls","C0011430"
> "701","dentin dysplasia","mondo","0015613"
> "0110339","osteogenesis imperfecta type 3","icd10cm","Q78.0"
> "0110339","osteogenesis imperfecta type 3","mondo","0009804"
> "0110338","osteogenesis imperfecta type 17","icd10cm","Q78.0"
> "0110338","osteogenesis imperfecta type 17","mondo","0014672"
> "0050819","Matthew-Wood syndrome","mondo","0011010"
> "0050818","transcobalamin II deficiency","mondo","0010149"
> "11885","ureteral benign neoplasm","mesh","D014516"
> "11885","ureteral benign neoplasm","umls","C0041955"
> "11885","ureteral benign neoplasm","mondo","0001398"
> "0050814","temtamy preaxial brachydactyly syndrome","mondo","0011533"
> "0050817","Stargardt disease","mondo","0019353"
> "0050816","urofacial syndrome","mesh","C536480"
> "0050816","urofacial syndrome","mondo","0000463"
> "0050811","congenital adrenal hyperplasia","icd10cm","E25"
> "0050811","congenital adrenal hyperplasia","icd10cm","E25.9"
> "0050811","congenital adrenal hyperplasia","icd9cm","255.2"
> "0050811","congenital adrenal hyperplasia","umls","C0701163"
> "0050811","congenital adrenal hyperplasia","mondo","0018479"
> "0050810","biotin deficiency","mesh","C531633"
> "0050810","biotin deficiency","mondo","0000461"
> "0050813","spondyloepiphyseal dysplasia with congenital joint dislocations","mondo","0007738"
> "0050812","spondyloepimetaphyseal dysplasia, Pakistani type","mondo","0013019"
> "5313","vulvar alveolar soft part sarcoma","umls","C1520069"
> "5313","vulvar alveolar soft part sarcoma","mondo","0003391"
> "5310","glycogen-rich clear cell breast carcinoma","umls","C0334319"
> "5310","glycogen-rich clear cell breast carcinoma","umls","C1512224"
> "5310","glycogen-rich clear cell breast carcinoma","mondo","0003390"
> "13027","transient global amnesia","icd10cm","G45.4"
> "13027","transient global amnesia","icd9cm","437.7"
> "13027","transient global amnesia","mesh","D020236"
> "13027","transient global amnesia","umls","C0338591"
> "13027","transient global amnesia","mondo","0001617"
> "13026","lobomycosis","icd10cm","B48.0"
> "13026","lobomycosis","icd9cm","116.2"
> "13026","lobomycosis","mesh","D060368"
> "13026","lobomycosis","umls","C0152066"
> "13026","lobomycosis","mondo","0001616"
> "13025","retinopathy of prematurity","icd10cm","H35.1"
> "13025","retinopathy of prematurity","icd10cm","H35.10"
> "13025","retinopathy of prematurity","icd10cm","H35.17"
> "13025","retinopathy of prematurity","icd9cm","362.20"
> "13025","retinopathy of prematurity","icd9cm","362.21"
> "13025","retinopathy of prematurity","mesh","D012178"
> "13025","retinopathy of prematurity","umls","C0035344"
> "13025","retinopathy of prematurity","mondo","0006952"
> "0060289","Ohdo syndrome","mesh","C536232"
> "0060289","Ohdo syndrome","umls","C0796094"
> "0060289","Ohdo syndrome","mondo","0000734"
> "0060288","omodysplasia","mesh","C537746"
> "0060288","omodysplasia","mesh","C567664"
> "0060288","omodysplasia","umls","C1850318"
> "0060288","omodysplasia","umls","C2750355"
> "0060288","omodysplasia","mondo","0017136"
> "0060283","peeling skin syndrome","icd10cm","Q80.8"
> "0060283","peeling skin syndrome","mondo","0019347"
> "0060282","persistent hyperplastic primary vitreous","mesh","D054514"
> "0060282","persistent hyperplastic primary vitreous","umls","C0266568"
> "0060282","persistent hyperplastic primary vitreous","mondo","0019631"
> "0060281","photosensitive epilepsy","icd10cm","G40.8"
> "0060281","photosensitive epilepsy","mondo","0015643"
> "0060280","primary pigmented nodular adrenocortical disease","mesh","C566469"
> "0060280","primary pigmented nodular adrenocortical disease","mesh","C566472"
> "0060280","primary pigmented nodular adrenocortical disease","umls","C1864846"
> "0060280","primary pigmented nodular adrenocortical disease","umls","C1864851"
> "0060280","primary pigmented nodular adrenocortical disease","mondo","0015999"
> "0060287","cornea plana","icd10cm","Q13.4"
> "0060287","cornea plana","mondo","0000733"
> "0060286","combined oxidative phosphorylation deficiency","mondo","0000732"
> "0060285","parietal foramina","mesh","C566826"
> "0060285","parietal foramina","umls","C1868598"
> "0060285","parietal foramina","mondo","0018953"
> "0060284","paroxysmal nocturnal hemoglobinuria","icd10cm","D59.1"
> "0060284","paroxysmal nocturnal hemoglobinuria","icd10cm","D59.5"
> "0060284","paroxysmal nocturnal hemoglobinuria","icd10cm","D59.6"
> "0060284","paroxysmal nocturnal hemoglobinuria","mesh","D006457"
> "0060284","paroxysmal nocturnal hemoglobinuria","umls","C0019050"
> "0060284","paroxysmal nocturnal hemoglobinuria","umls","C0024790"
> "0060284","paroxysmal nocturnal hemoglobinuria","umls","C0086774"
> "0060284","paroxysmal nocturnal hemoglobinuria","mondo","0018641"
> "3153","lipomatosis","icd10cm","E88.2"
> "3153","lipomatosis","mesh","D008068"
> "3153","lipomatosis","umls","C0023801"
> "3153","lipomatosis","mondo","0006574"
> "3151","skin squamous cell carcinoma","umls","C0553723"
> "3151","skin squamous cell carcinoma","mondo","0002529"
> "11088","asphyxia neonatorum","icd10cm","P84"
> "11088","asphyxia neonatorum","icd9cm","768.9"
> "11088","asphyxia neonatorum","mesh","D001238"
> "11088","asphyxia neonatorum","umls","C0004045"
> "11088","asphyxia neonatorum","mondo","0006663"
> "3156","hypomelanosis of Ito","mesh","D010859"
> "3156","hypomelanosis of Ito","umls","C0022283"
> "3156","hypomelanosis of Ito","mondo","0010302"
> "3210","Pelizaeus-Merzbacher disease","mesh","D020371"
> "3210","Pelizaeus-Merzbacher disease","umls","C0205711"
> "3210","Pelizaeus-Merzbacher disease","mondo","0010714"
> "3159","photosensitivity disease","mesh","D010787"
> "3159","photosensitivity disease","umls","C0031762"
> "3159","photosensitivity disease","mondo","0006597"
> "3158","hand dermatosis","mesh","D006229"
> "3158","hand dermatosis","umls","C0018567"
> "3158","hand dermatosis","mondo","0006556"
> "11086","chorioretinal scar","icd10cm","H31.0"
> "11086","chorioretinal scar","icd10cm","H31.00"
> "11086","chorioretinal scar","icd9cm","363.3"
> "11086","chorioretinal scar","icd9cm","363.30"
> "11086","chorioretinal scar","umls","C0008512"
> "11086","chorioretinal scar","mondo","0001193"
> "1637","breast angiomatosis","umls","C1511284"
> "1637","breast angiomatosis","mondo","0002064"
> "13867","focal labyrinthitis","icd9cm","386.32"
> "13867","focal labyrinthitis","umls","C0155505"
> "13867","focal labyrinthitis","mondo","0001820"
> "2485","phosphorus metabolism disease","icd9cm","275.3"
> "2485","phosphorus metabolism disease","mesh","D010760"
> "2485","phosphorus metabolism disease","umls","C0031707"
> "2485","phosphorus metabolism disease","mondo","0002319"
> "13359","Ehlers-Danlos syndrome","icd10cm","Q79.6"
> "13359","Ehlers-Danlos syndrome","icd9cm","756.83"
> "13359","Ehlers-Danlos syndrome","mesh","D004535"
> "13359","Ehlers-Danlos syndrome","umls","C0013720"
> "13359","Ehlers-Danlos syndrome","mondo","0020066"
> "10649","acute inferolateral myocardial infarction","icd9cm","410.20"
> "10649","acute inferolateral myocardial infarction","umls","C0155636"
> "10649","acute inferolateral myocardial infarction","mondo","0001089"
> "10646","schizotypal personality disorder","icd10cm","F21"
> "10646","schizotypal personality disorder","icd9cm","301.22"
> "10646","schizotypal personality disorder","mesh","D012569"
> "10646","schizotypal personality disorder","umls","C0036363"
> "10646","schizotypal personality disorder","mondo","0001087"
> "0110557","autosomal dominant nonsyndromic deafness 28","icd10cm","H90.3"
> "0110557","autosomal dominant nonsyndromic deafness 28","mondo","0012083"
> "0110556","autosomal dominant nonsyndromic deafness 27","icd10cm","H90.3"
> "0110556","autosomal dominant nonsyndromic deafness 27","mondo","0012902"
> "0110555","autosomal dominant nonsyndromic deafness 25","icd10cm","H90.3"
> "0110555","autosomal dominant nonsyndromic deafness 25","mondo","0011568"
> "0110554","autosomal dominant nonsyndromic deafness 24","icd10cm","H90.3"
> "0110554","autosomal dominant nonsyndromic deafness 24","mondo","0011657"
> "0110553","autosomal dominant nonsyndromic deafness 23","icd10cm","H90.3"
> "0110553","autosomal dominant nonsyndromic deafness 23","mondo","0011519"
> "0110552","autosomal dominant nonsyndromic deafness 22","icd10cm","H90.3"
> "0110552","autosomal dominant nonsyndromic deafness 22","mondo","0011660"
> "0110551","autosomal dominant nonsyndromic deafness 21","icd10cm","H90.3"
> "0110551","autosomal dominant nonsyndromic deafness 21","mondo","0011761"
> "0110550","autosomal dominant nonsyndromic deafness 20","icd10cm","H90.3"
> "0110550","autosomal dominant nonsyndromic deafness 20","mondo","0011480"
> "8574","lichen disease","icd10cm","L28.0"
> "8574","lichen disease","icd9cm","697"
> "8574","lichen disease","icd9cm","697.9"
> "8574","lichen disease","umls","C0023643"
> "8574","lichen disease","mondo","0006570"
> "8577","ulcerative colitis","icd10cm","K51"
> "8577","ulcerative colitis","icd10cm","K51.9"
> "8577","ulcerative colitis","icd9cm","556"
> "8577","ulcerative colitis","icd9cm","556.5"
> "8577","ulcerative colitis","icd9cm","556.9"
> "8577","ulcerative colitis","mesh","D003093"
> "8577","ulcerative colitis","umls","C0009324"
> "8577","ulcerative colitis","umls","C0375359"
> "8577","ulcerative colitis","mondo","0005101"
> "8573","lichen nitidus","icd10cm","L44.1"
> "8573","lichen nitidus","icd9cm","697.1"
> "8573","lichen nitidus","mesh","D017513"
> "8573","lichen nitidus","umls","C0162849"
> "8573","lichen nitidus","mondo","0006571"
> "8578","soft palate cancer","icd10cm","C05.1"
> "8578","soft palate cancer","icd9cm","145.3"
> "8578","soft palate cancer","umls","C0153376"
> "8578","soft palate cancer","mondo","0004611"
> "12573","neonatal thyrotoxicosis","icd10cm","P72.1"
> "12573","neonatal thyrotoxicosis","icd9cm","775.3"
> "12573","neonatal thyrotoxicosis","umls","C0158983"
> "12573","neonatal thyrotoxicosis","mondo","0001555"
> "12570","phacolytic glaucoma","icd9cm","365.51"
> "12570","phacolytic glaucoma","umls","C0152137"
> "12570","phacolytic glaucoma","mondo","0001553"
> "12571","phacogenic glaucoma","icd9cm","365.59"
> "12571","phacogenic glaucoma","umls","C0154959"
> "12571","phacogenic glaucoma","mondo","0001554"
> "12577","urethral obstruction","mesh","D014524"
> "12577","urethral obstruction","umls","C0041972"
> "12577","urethral obstruction","mondo","0001556"
> "12574","posterior uveitis","mesh","D015866"
> "12574","posterior uveitis","umls","C0042167"
> "12574","posterior uveitis","mondo","0006918"
> "0060755","familial temporal lobe epilepsy 2","mondo","0011965"
> "0060754","familial temporal lobe epilepsy 8","mondo","0014650"
> "0060757","sclerosteosis 2","icd10cm","M85.2"
> "0060757","sclerosteosis 2","mondo","0013679"
> "0060756","sclerosteosis 1","icd10cm","M85.2"
> "0060756","sclerosteosis 1","mondo","0010016"
> "0060023","immunodeficiency with hyper IgM type 3","mondo","0011735"
> "0060022","CD40 ligand deficiency","mondo","0010626"
> "0060753","familial temporal lobe epilepsy 4","mondo","0012706"
> "0060752","familial temporal lobe epilepsy 5","mondo","0013741"
> "0060759","immunodeficiency with hyper IgM type 5","icd10cm","D80.5"
> "0060759","immunodeficiency with hyper IgM type 5","mondo","0011971"
> "0060758","immunodeficiency with hyper-IgM type 2","icd10cm","D80.5"
> "0060758","immunodeficiency with hyper-IgM type 2","mondo","0011528"
> "7402","L-cell glucagon-like peptide producing tumor","umls","C3274140"
> "7402","L-cell glucagon-like peptide producing tumor","mondo","0004211"
> "2816","malignant oculomotor nerve tumor","umls","C0686417"
> "2816","malignant oculomotor nerve tumor","mondo","0002434"
> "6629","nipple carcinoma","umls","C1334966"
> "6629","nipple carcinoma","mondo","0003950"
> "6627","cervical adenoma malignum","umls","C1516423"
> "6627","cervical adenoma malignum","mondo","0006140"
> "6620","X-linked hyper IgM syndrome","mesh","D053306"
> "6620","X-linked hyper IgM syndrome","umls","C0272236"
> "6620","X-linked hyper IgM syndrome","mondo","0010626"
> "6621","cerebral angioma","umls","C0877388"
> "6621","cerebral angioma","mondo","0003948"
> "0080269","autosomal dominant nonsyndromic deafness 73","mondo","0033260"
> "0080268","autosomal dominant nonsyndromic deafness 72","mondo","0033259"
> "0080267","autosomal dominant nonsyndromic deafness 71","mondo","0033258"
> "0080266","primary ciliary dyskinesia 37","mondo","0033204"
> "0080265","nephrotic syndrome type 14","mondo","0033203"
> "0080264","exudative vitreoretinopathy 7","mondo","0033123"
> "0080263","autosomal recessive nonsyndromic deafness 108","mondo","0033200"
> "0080262","autosomal recessive nonsyndromic deafness 107","mondo","0033199"
> "0080261","autosomal recessive nonsyndromic deafness 106","mondo","0033198"
> "0080260","autosomal recessive spinocerebellar ataxia 26","mondo","0033116"
> "4715","gastric neuroendocrine neoplasm","umls","C1333783"
> "4715","gastric neuroendocrine neoplasm","mondo","0003111"
> "4716","malignant gastric germ cell tumor","umls","C1333769"
> "4716","malignant gastric germ cell tumor","mondo","0003112"
> "4717","extragonadal germ cell cancer","umls","C0262963"
> "4717","extragonadal germ cell cancer","umls","C1334581"
> "4717","extragonadal germ cell cancer","mondo","0003113"
> "13620","patent foramen ovale","icd10cm","Q21.1"
> "13620","patent foramen ovale","mesh","D054092"
> "13620","patent foramen ovale","umls","C0016522"
> "13620","patent foramen ovale","mondo","0020439"
> "13622","campylobacteriosis","mesh","D002169"
> "13622","campylobacteriosis","umls","C0006818"
> "13622","campylobacteriosis","mondo","0005688"
> "2338","mandibular cancer","icd10cm","C41.1"
> "2338","mandibular cancer","icd9cm","170.1"
> "2338","mandibular cancer","mesh","D008339"
> "2338","mandibular cancer","umls","C0024694"
> "2338","mandibular cancer","umls","C0153511"
> "2338","mandibular cancer","mondo","0005837"
> "2339","Crouzon syndrome","icd10cm","Q75.1"
> "2339","Crouzon syndrome","mesh","D003394"
> "2339","Crouzon syndrome","umls","C0010273"
> "2339","Crouzon syndrome","mondo","0007405"
> "13629","dentine erosion","icd9cm","521.32"
> "13629","dentine erosion","umls","C1456162"
> "13629","dentine erosion","mondo","0001762"
> "4719","bone giant cell sarcoma","umls","C0334552"
> "4719","bone giant cell sarcoma","mondo","0006287"
> "0111164","molybdenum cofactor deficiency type A","mesh","C565372"
> "0111164","molybdenum cofactor deficiency type A","umls","C1854988"
> "0111164","molybdenum cofactor deficiency type A","mondo","0009643"
> "14702","branchiootorenal syndrome","mesh","D019280"
> "14702","branchiootorenal syndrome","umls","C0265234"
> "14702","branchiootorenal syndrome","mondo","0007029"
> "0110698","hypotrichosis 1","mondo","0011549"
> "3717","gastric adenocarcinoma","umls","C0278701"
> "3717","gastric adenocarcinoma","mondo","0005036"
> "3716","mucinous stomach adenocarcinoma","umls","C1334809"
> "3716","mucinous stomach adenocarcinoma","mondo","0006309"
> "0050569","Seckel syndrome","icd10cm","Q87.1"
> "0050569","Seckel syndrome","mondo","0019342"
> "0050568","spondylocostal dysostosis","mondo","0000359"
> "3713","ovary adenocarcinoma","umls","C0948216"
> "3713","ovary adenocarcinoma","mondo","0002752"
> "0110699","hypotrichosis 2","mondo","0007805"
> "0050565","autosomal recessive nonsyndromic deafness","icd10cm","H90.3"
> "0050565","autosomal recessive nonsyndromic deafness","mondo","0019588"
> "0050564","autosomal dominant nonsyndromic deafness","icd10cm","H90.3"
> "0050564","autosomal dominant nonsyndromic deafness","mondo","0019587"
> "0050567","orofacial cleft","mondo","0000358"
> "0050566","X-linked nonsyndromic deafness","icd10cm","H90.3"
> "0050566","X-linked nonsyndromic deafness","mondo","0019586"
> "0050561","Lennox-Gastaut syndrome","mondo","0016532"
> "0050560","Walker-Warburg syndrome","mesh","D058494"
> "0050560","Walker-Warburg syndrome","mondo","0019523"
> "0050562","West syndrome","mesh","D013036"
> "0050562","West syndrome","mondo","0018097"
> "4908","anal carcinoma","mesh","D001005"
> "4908","anal carcinoma","umls","C0279637"
> "4908","anal carcinoma","mondo","0003199"
> "4679","breast mucoepidermoid carcinoma","umls","C1334813"
> "4679","breast mucoepidermoid carcinoma","mondo","0003087"
> "4678","thymus mucoepidermoid carcinoma","umls","C1334814"
> "4678","thymus mucoepidermoid carcinoma","mondo","0003086"
> "4901","peritoneal serous adenocarcinoma","umls","C1514429"
> "4901","peritoneal serous adenocarcinoma","mondo","0003195"
> "4676","uremia","icd10cm","N19"
> "4676","uremia","mesh","D014511"
> "4676","uremia","umls","C0041948"
> "4676","uremia","mondo","0007008"
> "4903","granular cell carcinoma","mesh","D000230"
> "4903","granular cell carcinoma","umls","C0205644"
> "4903","granular cell carcinoma","mondo","0003197"
> "4902","appendix carcinoma","umls","C0728951"
> "4902","appendix carcinoma","mondo","0003196"
> "4905","pancreatic carcinoma","mesh","C562463"
> "4905","pancreatic carcinoma","umls","C0235974"
> "4905","pancreatic carcinoma","mondo","0005192"
> "4907","small intestine carcinoma","umls","C0238196"
> "4907","small intestine carcinoma","mondo","0005522"
> "4906","small intestine adenocarcinoma","umls","C0278803"
> "4906","small intestine adenocarcinoma","mondo","0003198"
> "11705","impaired renal function disease","icd9cm","588.8"
> "11705","impaired renal function disease","icd9cm","588.89"
> "11705","impaired renal function disease","umls","C0029791"
> "11705","impaired renal function disease","mondo","0001343"
> "11701","selective IgA deficiency disease","mesh","D017098"
> "11701","selective IgA deficiency disease","umls","C0162538"
> "11701","selective IgA deficiency disease","mondo","0001341"
> "11702","dysgammaglobulinemia","mesh","D004406"
> "11702","dysgammaglobulinemia","umls","C0013374"
> "11702","dysgammaglobulinemia","mondo","0001342"
> "5149","epithelioid neurofibroma","umls","C1275264"
> "5149","epithelioid neurofibroma","mondo","0003302"
> "5146","appendix leiomyoma","umls","C1332327"
> "5146","appendix leiomyoma","mondo","0003300"
> "5147","dartoic leiomyoma","umls","C0346066"
> "5147","dartoic leiomyoma","mondo","0003301"
> "5142","vulvar leiomyoma","umls","C1520087"
> "5142","vulvar leiomyoma","mondo","0003298"
> "5143","large bowel leiomyoma","umls","C1333113"
> "5143","large bowel leiomyoma","mondo","0003299"
> "5140","gallbladder leiomyoma","umls","C1333745"
> "5140","gallbladder leiomyoma","mondo","0003297"
> "120","female reproductive organ cancer","icd10cm","C57"
> "120","female reproductive organ cancer","icd9cm","184"
> "120","female reproductive organ cancer","mesh","D005833"
> "120","female reproductive organ cancer","umls","C0017416"
> "120","female reproductive organ cancer","umls","C0153585"
> "120","female reproductive organ cancer","umls","C0699889"
> "120","female reproductive organ cancer","mondo","0001416"
> "121","vaginal disease","mesh","D014623"
> "121","vaginal disease","umls","C0042251"
> "121","vaginal disease","mondo","0001433"
> "125","vagina leiomyoma","umls","C1336939"
> "125","vagina leiomyoma","mondo","0001536"
> "127","leiomyoma","mesh","D007889"
> "127","leiomyoma","umls","C0023267"
> "127","leiomyoma","mondo","0001572"
> "10699","paragonimiasis","icd10cm","B66.4"
> "10699","paragonimiasis","icd9cm","121.2"
> "10699","paragonimiasis","mesh","D010237"
> "10699","paragonimiasis","umls","C0030424"
> "10699","paragonimiasis","mondo","0005895"
> "3379","metachronous osteosarcoma of the bone","umls","C1334704"
> "3379","metachronous osteosarcoma of the bone","mondo","0002632"
> "10349","solitary cyst of breast","icd10cm","N60.0"
> "10349","solitary cyst of breast","icd10cm","N60.09"
> "10349","solitary cyst of breast","icd9cm","610.0"
> "10349","solitary cyst of breast","umls","C0037619"
> "10349","solitary cyst of breast","mondo","0001009"
> "3377","small cell osteogenic sarcoma","umls","C0279622"
> "3377","small cell osteogenic sarcoma","mondo","0002630"
> "1187","tibial neuropathy","mesh","D020429"
> "1187","tibial neuropathy","umls","C0751932"
> "1187","tibial neuropathy","mondo","0006997"
> "1184","nephrotic syndrome","icd10cm","N04"
> "1184","nephrotic syndrome","icd9cm","581"
> "1184","nephrotic syndrome","mesh","D009404"
> "1184","nephrotic syndrome","umls","C0027726"
> "1184","nephrotic syndrome","mondo","0005377"
> "9169","Wiskott-Aldrich syndrome","icd10cm","D82.0"
> "9169","Wiskott-Aldrich syndrome","icd9cm","279.12"
> "9169","Wiskott-Aldrich syndrome","mesh","D014923"
> "9169","Wiskott-Aldrich syndrome","umls","C0043194"
> "9169","Wiskott-Aldrich syndrome","mondo","0010518"
> "3374","peripheral osteosarcoma","umls","C1332591"
> "3374","peripheral osteosarcoma","mondo","0002628"
> "0070129","autosomal recessive cutis laxa type IID","icd10cm","Q82.8"
> "0070129","autosomal recessive cutis laxa type IID","mondo","0027451"
> "3373","juxtacortical osteosarcoma","mesh","D018217"
> "3373","juxtacortical osteosarcoma","umls","C0206642"
> "3373","juxtacortical osteosarcoma","mondo","0006817"
> "0070127","congenital nongoitrous hypothyroidism 3","icd10cm","E03.1"
> "0070127","congenital nongoitrous hypothyroidism 3","mondo","0012360"
> "0070126","congenital nongoitrous hypothyroidism 1","icd10cm","E03.1"
> "0070126","congenital nongoitrous hypothyroidism 1","mondo","0010142"
> "10341","chronic meningitis","icd10cm","G03.1"
> "10341","chronic meningitis","icd9cm","322.2"
> "10341","chronic meningitis","umls","C0154653"
> "10341","chronic meningitis","mondo","0001007"
> "0070181","spermatogenic failure 23","mondo","0054727"
> "0070180","spermatogenic failure 11","mondo","0014037"
> "0070183","spermatogenic failure 5","umls","C0403812"
> "0070183","spermatogenic failure 5","mondo","0009461"
> "0070182","spermatogenic failure 13","mondo","0014365"
> "0070185","X-linked spermatogenic failure 2","mondo","0010647"
> "0070184","spermatogenic failure 16","mondo","0014961"
> "0070187","Y-linked spermatogenic failure 2","mondo","0010767"
> "0070186","Y-linked spermatogenic failure 1","mondo","0010763"
> "0070189","X-linked spermatogenic failure 1","mondo","0056795"
> "0070188","spermatogenic failure 1","mondo","0009776"
> "0070122","Meckel syndrome 8","icd10cm","Q61.9"
> "0070122","Meckel syndrome 8","mondo","0013482"
> "0110108","atrial heart septal defect 3","icd10cm","Q21.1"
> "0110108","atrial heart septal defect 3","mondo","0013567"
> "7959","duodenal gastrinoma","umls","C1333321"
> "7959","duodenal gastrinoma","mondo","0004411"
> "0110104","atopic dermatitis 8","mondo","0013294"
> "0110105","atopic dermatitis 9","mondo","0013295"
> "0110106","atrial heart septal defect 1","icd10cm","Q21.1"
> "0110106","atrial heart septal defect 1","mondo","0007172"
> "7958","sarcomatoid penile squamous cell carcinoma","umls","C1335923"
> "7958","sarcomatoid penile squamous cell carcinoma","mondo","0004410"
> "0110100","atopic dermatitis 4","mondo","0011598"
> "0110101","atopic dermatitis 5","mondo","0011608"
> "0110102","atopic dermatitis 6","mondo","0011609"
> "0110103","atopic dermatitis 7","mondo","0013107"
> "6823","pancreatoblastoma","mesh","C537162"
> "6823","pancreatoblastoma","umls","C0334489"
> "6823","pancreatoblastoma","mondo","0019035"
> "6827","pancreatic solid pseudopapillary carcinoma","umls","C1336029"
> "6827","pancreatic solid pseudopapillary carcinoma","mondo","0018525"
> "10544","pylorus cancer","icd10cm","C16.4"
> "10544","pylorus cancer","icd9cm","151.1"
> "10544","pylorus cancer","umls","C0153418"
> "10544","pylorus cancer","mondo","0001061"
> "10547","pyloric antrum cancer","icd10cm","C16.3"
> "10547","pyloric antrum cancer","icd9cm","151.2"
> "10547","pyloric antrum cancer","umls","C0153419"
> "10547","pyloric antrum cancer","mondo","0001062"
> "0110169","Charcot-Marie-Tooth disease axonal type 2P","icd10cm","G60.0"
> "0110169","Charcot-Marie-Tooth disease axonal type 2P","mondo","0013753"
> "10541","microinvasive gastric cancer","umls","C0349530"
> "10541","microinvasive gastric cancer","mondo","0001060"
> "10540","gastric lymphoma","mesh","C535648"
> "10540","gastric lymphoma","umls","C0349532"
> "10540","gastric lymphoma","mondo","0001059"
> "10548","cardia cancer","icd10cm","C16.0"
> "10548","cardia cancer","icd9cm","151.0"
> "10548","cardia cancer","umls","C0153417"
> "10548","cardia cancer","mondo","0001063"
> "2229","factor XI deficiency","icd10cm","D68.1"
> "2229","factor XI deficiency","icd9cm","286.2"
> "2229","factor XI deficiency","mesh","D005173"
> "2229","factor XI deficiency","umls","C0015523"
> "2229","factor XI deficiency","mondo","0012897"
> "14283","primary hypertrophic osteoarthropathy","icd10cm","M89.4"
> "14283","primary hypertrophic osteoarthropathy","mesh","D010004"
> "14283","primary hypertrophic osteoarthropathy","umls","C0029411"
> "14283","primary hypertrophic osteoarthropathy","mondo","0016620"
> "14286","neurogenic arthropathy","icd10cm","M14.6"
> "14286","neurogenic arthropathy","icd9cm","713.5"
> "14286","neurogenic arthropathy","mesh","D001177"
> "14286","neurogenic arthropathy","umls","C0003892"
> "14286","neurogenic arthropathy","mondo","0001935"
> "14287","brawny scleritis","icd10cm","H15.02"
> "14287","brawny scleritis","icd9cm","379.06"
> "14287","brawny scleritis","umls","C0155356"
> "14287","brawny scleritis","mondo","0001936"
> "14284","patellofemoral pain syndrome","mesh","D046788"
> "14284","patellofemoral pain syndrome","umls","C0877149"
> "14284","patellofemoral pain syndrome","mondo","0006894"
> "0110163","Charcot-Marie-Tooth disease axonal type 2F","icd10cm","G60.0"
> "0110163","Charcot-Marie-Tooth disease axonal type 2F","mondo","0011687"
> "14289","Ebstein anomaly","icd10cm","Q22.5"
> "14289","Ebstein anomaly","icd9cm","746.2"
> "14289","Ebstein anomaly","mesh","D004437"
> "14289","Ebstein anomaly","umls","C0013481"
> "14289","Ebstein anomaly","mondo","0009144"
> "6495","adult myxoid chondrosarcoma","umls","C1332209"
> "6495","adult myxoid chondrosarcoma","mondo","0003899"
> "8211","fallopian tube cystadenofibroma","umls","C1517111"
> "8211","fallopian tube cystadenofibroma","mondo","0004501"
> "8743","erythema infectiosum","icd10cm","B08.3"
> "8743","erythema infectiosum","icd9cm","057.0"
> "8743","erythema infectiosum","mesh","D016731"
> "8743","erythema infectiosum","umls","C0085273"
> "8743","erythema infectiosum","mondo","0006544"
> "0070282","primary autosomal recessive microcephaly 8","mondo","0013849"
> "8216","parapharyngeal meningioma","umls","C1335345"
> "8216","parapharyngeal meningioma","mondo","0004502"
> "7650","pulmonary type ovarian small cell carcinoma","umls","C1518737"
> "7650","pulmonary type ovarian small cell carcinoma","mondo","0004318"
> "7651","small-cell carcinoma of the ovary of hypercalcemic type","umls","C1518736"
> "7651","small-cell carcinoma of the ovary of hypercalcemic type","mondo","0004319"
> "7656","adult infiltrating astrocytic neoplasm","umls","C0281329"
> "7656","adult infiltrating astrocytic neoplasm","mondo","0004320"
> "0060569","hypertrichotic osteochondrodysplasia Cantu type","mesh","C535572"
> "0060569","hypertrichotic osteochondrodysplasia Cantu type","mondo","0009406"
> "0060562","anomalous left coronary artery from the pulmonary artery","mesh","D063748"
> "0060562","anomalous left coronary artery from the pulmonary artery","mondo","0000811"
> "0060563","Char syndrome","mesh","C566815"
> "0060563","Char syndrome","mondo","0008209"
> "0060560","lethal congenital contracture syndrome 2","mesh","C564369"
> "0060560","lethal congenital contracture syndrome 2","mondo","0011868"
> "8177","endocervical type cervical adenomyoma","umls","C1516405"
> "8177","endocervical type cervical adenomyoma","mondo","0004486"
> "0060566","Holzgreve-Wagner-Rehder Syndrome","mesh","C535327"
> "0060566","Holzgreve-Wagner-Rehder Syndrome","umls","C1856095"
> "0060566","Holzgreve-Wagner-Rehder Syndrome","mondo","0009350"
> "0060567","erythema elevatum diutinum","icd10cm","L95.1"
> "0060567","erythema elevatum diutinum","mesh","C535509"
> "0060567","erythema elevatum diutinum","umls","C0263398"
> "0060567","erythema elevatum diutinum","mondo","0019526"
> "0060565","Ritscher-Schinzel syndrome","mesh","C535313"
> "0060565","Ritscher-Schinzel syndrome","umls","C0796137"
> "0060565","Ritscher-Schinzel syndrome","mondo","0019078"
> "13956","uterine corpus myxoid leiomyoma","umls","C1519860"
> "13956","uterine corpus myxoid leiomyoma","mondo","0001844"
> "13953","uterine corpus dissecting leiomyoma","umls","C1519847"
> "13953","uterine corpus dissecting leiomyoma","mondo","0001842"
> "9869","hereditary fructose intolerance syndrome","icd10cm","E74.12"
> "9869","hereditary fructose intolerance syndrome","icd9cm","271.2"
> "9869","hereditary fructose intolerance syndrome","mesh","D005633"
> "9869","hereditary fructose intolerance syndrome","umls","C0016751"
> "9869","hereditary fructose intolerance syndrome","mondo","0009249"
> "9868","intestinal disaccharidase deficiency","icd9cm","271.3"
> "9868","intestinal disaccharidase deficiency","umls","C0021830"
> "9868","intestinal disaccharidase deficiency","mondo","0004905"
> "9861","miliary tuberculosis","icd10cm","A19"
> "9861","miliary tuberculosis","icd10cm","A19.9"
> "9861","miliary tuberculosis","icd9cm","018"
> "9861","miliary tuberculosis","icd9cm","018.9"
> "9861","miliary tuberculosis","icd9cm","018.90"
> "9861","miliary tuberculosis","mesh","D014391"
> "9861","miliary tuberculosis","umls","C0041321"
> "9861","miliary tuberculosis","mondo","0005848"
> "2225","obsolete megakaryocytic tumor","umls","C1334687"
> "9867","toxic maculopathy","icd10cm","H35.38"
> "9867","toxic maculopathy","icd9cm","362.55"
> "9867","toxic maculopathy","umls","C0271086"
> "9867","toxic maculopathy","mondo","0004904"
> "0110892","inflammatory bowel disease 1","mondo","0009960"
> "14427","abnormality of glucagon secretion","icd9cm","251.4"
> "14427","abnormality of glucagon secretion","umls","C0154191"
> "14427","abnormality of glucagon secretion","mondo","0001962"
> "2300","spondylolysis","icd10cm","M43.0"
> "2300","spondylolysis","icd10cm","M43.00"
> "2300","spondylolysis","mesh","D013169"
> "2300","spondylolysis","umls","C0038018"
> "2300","spondylolysis","mondo","0005541"
> "10744","broad ligament malignant neoplasm","icd10cm","C57.1"
> "10744","broad ligament malignant neoplasm","icd9cm","183.3"
> "10744","broad ligament malignant neoplasm","umls","C0346866"
> "10744","broad ligament malignant neoplasm","mondo","0001108"
> "14422","dipetalonemiasis","icd9cm","125.4"
> "14422","dipetalonemiasis","mesh","D004154"
> "14422","dipetalonemiasis","umls","C0012517"
> "14422","dipetalonemiasis","mondo","0005731"
> "14423","glossopharyngeal neuralgia","icd10cm","G52.1"
> "14423","glossopharyngeal neuralgia","icd9cm","352.1"
> "14423","glossopharyngeal neuralgia","mesh","D020435"
> "14423","glossopharyngeal neuralgia","umls","C0154731"
> "14423","glossopharyngeal neuralgia","mondo","0016372"
> "12275","cutaneous diphtheria","icd10cm","A36.3"
> "12275","cutaneous diphtheria","icd9cm","032.85"
> "12275","cutaneous diphtheria","umls","C0012555"
> "12275","cutaneous diphtheria","mondo","0001479"
> "0110893","inflammatory bowel disease 13","mondo","0012831"
> "10742","cerebral lipidosis","icd9cm","330.1"
> "10742","cerebral lipidosis","umls","C0007788"
> "10742","cerebral lipidosis","mondo","0020143"
> "1519","cecum carcinoma","umls","C0149640"
> "1519","cecum carcinoma","mondo","0006029"
> "1518","cecal disease","mesh","D002429"
> "1518","cecal disease","umls","C0007527"
> "1518","cecal disease","mondo","0002031"
> "1517","cecal benign neoplasm","mesh","D002430"
> "1517","cecal benign neoplasm","umls","C0007528"
> "1517","cecal benign neoplasm","mondo","0005694"
> "1510","personality disorder","icd9cm","301.8"
> "1510","personality disorder","icd9cm","301.89"
> "1510","personality disorder","umls","C0029707"
> "1510","personality disorder","mondo","0002028"
> "1513","chronic cervicitis","umls","C0269062"
> "1513","chronic cervicitis","mondo","0002030"
> "1512","chronic gonorrhea of cervix","icd9cm","098.35"
> "1512","chronic gonorrhea of cervix","umls","C0153206"
> "1512","chronic gonorrhea of cervix","mondo","0002029"
> "14669","acrodysostosis","mesh","C538179"
> "14669","acrodysostosis","umls","C0220659"
> "14669","acrodysostosis","mondo","0019797"
> "13819","lymphogranuloma venereum","icd10cm","A55"
> "13819","lymphogranuloma venereum","icd9cm","099.1"
> "13819","lymphogranuloma venereum","mesh","D008219"
> "13819","lymphogranuloma venereum","umls","C0024286"
> "13819","lymphogranuloma venereum","mondo","0005834"
> "13814","hypoglossal nerve disease","icd10cm","G52.3"
> "13814","hypoglossal nerve disease","icd9cm","352.5"
> "13814","hypoglossal nerve disease","mesh","D020437"
> "13814","hypoglossal nerve disease","umls","C0152181"
> "13814","hypoglossal nerve disease","mondo","0001810"
> "0110890","inflammatory bowel disease 19","mondo","0012845"
> "13812","adhesions of uterus","umls","C0241593"
> "13812","adhesions of uterus","mondo","0001809"
> "13810","familial hypercholesterolemia","icd10cm","E78.00"
> "13810","familial hypercholesterolemia","icd10cm","E78.01"
> "13810","familial hypercholesterolemia","mesh","D006938"
> "13810","familial hypercholesterolemia","umls","C0020445"
> "13810","familial hypercholesterolemia","mondo","0005439"
> "13811","chronic subinvolution of uterus","icd9cm","621.1"
> "13811","chronic subinvolution of uterus","umls","C0156370"
> "13811","chronic subinvolution of uterus","mondo","0001808"
> "11838","penis sarcoma","umls","C0238352"
> "11838","penis sarcoma","mondo","0001387"
> "11839","glans penis cancer","icd10cm","C60.1"
> "11839","glans penis cancer","icd9cm","187.2"
> "11839","glans penis cancer","umls","C0153599"
> "11839","glans penis cancer","mondo","0001388"
> "0110538","autosomal recessive nonsyndromic deafness 96","icd10cm","H90.3"
> "0110538","autosomal recessive nonsyndromic deafness 96","mondo","0013738"
> "0110891","inflammatory bowel disease 3","mondo","0011471"
> "11550","oculomotor nerve paralysis","icd10cm","H49.0"
> "11550","oculomotor nerve paralysis","mesh","D015840"
> "11550","oculomotor nerve paralysis","umls","C0028866"
> "11550","oculomotor nerve paralysis","mondo","0001309"
> "11552","Bowman's membrane folds or rupture","icd10cm","H18.31"
> "11552","Bowman's membrane folds or rupture","icd9cm","371.31"
> "11552","Bowman's membrane folds or rupture","umls","C0155115"
> "11552","Bowman's membrane folds or rupture","mondo","0001310"
> "11555","Fuchs' endothelial dystrophy","icd10cm","H18.51"
> "11555","Fuchs' endothelial dystrophy","mesh","D005642"
> "11555","Fuchs' endothelial dystrophy","umls","C0016781"
> "11555","Fuchs' endothelial dystrophy","mondo","0005321"
> "11554","Chandler syndrome","icd10cm","H18.51"
> "11554","Chandler syndrome","icd9cm","371.57"
> "11554","Chandler syndrome","mesh","D057129"
> "11554","Chandler syndrome","umls","C0544008"
> "11554","Chandler syndrome","mondo","0020369"
> "11557","acute serous otitis media","icd10cm","H65.0"
> "11557","acute serous otitis media","icd10cm","H65.00"
> "11557","acute serous otitis media","icd9cm","381.01"
> "11557","acute serous otitis media","umls","C0155415"
> "11557","acute serous otitis media","mondo","0001312"
> "0110896","inflammatory bowel disease 16","mondo","0012838"
> "11558","acute allergic serous otitis media","icd9cm","381.04"
> "11558","acute allergic serous otitis media","umls","C0155418"
> "11558","acute allergic serous otitis media","mondo","0001313"
> "0070285","primary autosomal recessive microcephaly 1","mondo","0009617"
> "13608","biliary atresia","icd10cm","Q44.2"
> "13608","biliary atresia","icd9cm","751.61"
> "13608","biliary atresia","mesh","D001656"
> "13608","biliary atresia","umls","C0005411"
> "13608","biliary atresia","mondo","0008867"
> "0110897","inflammatory bowel disease 15","mondo","0012837"
> "0111583","carboxypeptidase N deficiency","mesh","C562876"
> "0111583","carboxypeptidase N deficiency","umls","C0398782"
> "0110894","inflammatory bowel disease 11","mondo","0008617"
> "0111200","distal hereditary motor neuronopathy type 1","umls","C1866784"
> "0110928","nemaline myopathy 2","mondo","0009725"
> "0110929","nemaline myopathy 9","mondo","0014326"
> "0110926","nemaline myopathy 1","mondo","0012239"
> "0110927","nemaline myopathy 3","mondo","0008070"
> "0110924","familial hemophagocytic lymphohistiocytosis 4","mondo","0011336"
> "0110925","familial hemophagocytic lymphohistiocytosis 5","mondo","0013135"
> "0110922","familial hemophagocytic lymphohistiocytosis 2","mondo","0011337"
> "0110923","familial hemophagocytic lymphohistiocytosis 3","mondo","0012146"
> "0110920","hereditary spherocytosis type 5","mondo","0012985"
> "0110921","familial hemophagocytic lymphohistiocytosis 1","mondo","0009974"
> "0110895","inflammatory bowel disease 14","mondo","0012832"
> "0111196","X-linked distal spinal muscular atrophy 3","umls","C1845359"
> "263","kidney cancer","icd10cm","C64"
> "263","kidney cancer","icd9cm","189.0"
> "263","kidney cancer","mesh","D007680"
> "263","kidney cancer","umls","C0022665"
> "263","kidney cancer","umls","C0494158"
> "263","kidney cancer","umls","C0740457"
> "263","kidney cancer","mondo","0002367"
> "0110822","hereditary spastic paraplegia 77","icd10cm","G11.4"
> "0110822","hereditary spastic paraplegia 77","mondo","0014882"
> "0110821","hereditary spastic paraplegia 76","mondo","0014827"
> "0110820","hereditary spastic paraplegia 75","icd10cm","G11.4"
> "0110820","hereditary spastic paraplegia 75","mondo","0014729"
> "0110827","Usher syndrome type 2","mesh","D052245"
> "0110827","Usher syndrome type 2","umls","C0339534"
> "0110827","Usher syndrome type 2","umls","C1568249"
> "0110827","Usher syndrome type 2","mondo","0016484"
> "0110826","Usher syndrome type 1","icd10cm","H35.5"
> "0110826","Usher syndrome type 1","umls","C0339533"
> "0110826","Usher syndrome type 1","mondo","0010168"
> "265","spleen angiosarcoma","umls","C0346424"
> "265","spleen angiosarcoma","mondo","0002376"
> "264","hemangiopericytoma","mesh","D006393"
> "264","hemangiopericytoma","umls","C0018922"
> "264","hemangiopericytoma","mondo","0005094"
> "0110829","retinitis pigmentosa-deafness syndrome","mesh","D052245"
> "0110829","retinitis pigmentosa-deafness syndrome","umls","C1568248"
> "0110829","retinitis pigmentosa-deafness syndrome","mondo","0010775"
> "268","liver angiosarcoma","icd10cm","C22.3"
> "268","liver angiosarcoma","umls","C0345907"
> "268","liver angiosarcoma","mondo","0002387"
> "6015","adult central nervous system teratoma","umls","C1370506"
> "6015","adult central nervous system teratoma","mondo","0003731"
> "6017","central nervous system mature teratoma","umls","C1332886"
> "6017","central nervous system mature teratoma","mondo","0003733"
> "6016","adult central nervous system mature teratoma","umls","C1332194"
> "6016","adult central nervous system mature teratoma","mondo","0003732"
> "6019","central nervous system immature teratoma","umls","C1332883"
> "6019","central nervous system immature teratoma","mondo","0003735"
> "6018","adult central nervous system immature teratoma","umls","C1332193"
> "6018","adult central nervous system immature teratoma","mondo","0003734"
> "10605","short bowel syndrome","mesh","D012778"
> "10605","short bowel syndrome","umls","C0036992"
> "10605","short bowel syndrome","mondo","0015183"
> "9263","homocystinuria","icd10cm","E72.11"
> "9263","homocystinuria","mesh","D006712"
> "9263","homocystinuria","umls","C0019880"
> "9263","homocystinuria","mondo","0004737"
> "988","mitral valve prolapse","mesh","D008945"
> "988","mitral valve prolapse","umls","C0026267"
> "988","mitral valve prolapse","mondo","0004910"
> "9267","urea cycle disorder","icd10cm","E72.2"
> "9267","urea cycle disorder","icd10cm","E72.20"
> "9267","urea cycle disorder","icd9cm","270.6"
> "9267","urea cycle disorder","mesh","D056806"
> "9267","urea cycle disorder","umls","C0154246"
> "9267","urea cycle disorder","mondo","0004739"
> "9266","cystinuria","icd10cm","E72.01"
> "9266","cystinuria","mesh","D003555"
> "9266","cystinuria","umls","C0010691"
> "9266","cystinuria","mondo","0009067"
> "9265","histidine metabolism disease","icd10cm","E70.4"
> "9265","histidine metabolism disease","icd10cm","E70.40"
> "9265","histidine metabolism disease","icd9cm","270.5"
> "9265","histidine metabolism disease","umls","C0268512"
> "9265","histidine metabolism disease","mondo","0019228"
> "10040","malignant eyelid melanoma","umls","C0339116"
> "10040","malignant eyelid melanoma","mondo","0000928"
> "10041","dysplastic nevus syndrome","mesh","D004416"
> "10041","dysplastic nevus syndrome","umls","C0205747"
> "10041","dysplastic nevus syndrome","mondo","0007964"
> "9269","maple syrup urine disease","icd10cm","E71.0"
> "9269","maple syrup urine disease","mesh","D008375"
> "9269","maple syrup urine disease","umls","C0024776"
> "9269","maple syrup urine disease","mondo","0009563"
> "981","diffuse secondary choroid atrophy","icd10cm","H31.12"
> "981","diffuse secondary choroid atrophy","icd9cm","363.42"
> "981","diffuse secondary choroid atrophy","umls","C0154892"
> "981","diffuse secondary choroid atrophy","mondo","0004886"
> "986","alopecia areata","icd10cm","L63"
> "986","alopecia areata","icd10cm","L63.9"
> "986","alopecia areata","icd9cm","704.01"
> "986","alopecia areata","mesh","D000506"
> "986","alopecia areata","umls","C0002171"
> "986","alopecia areata","mondo","0005340"
> "987","alopecia","icd10cm","L65.9"
> "987","alopecia","icd9cm","704.0"
> "987","alopecia","icd9cm","704.00"
> "987","alopecia","mesh","D000505"
> "987","alopecia","umls","C0002170"
> "987","alopecia","mondo","0004907"
> "10047","nodular malignant melanoma","umls","C0334424"
> "10047","nodular malignant melanoma","mondo","0000930"
> "0080094","myofibrillar myopathy 3","icd10cm","G71.0"
> "0080094","myofibrillar myopathy 3","mondo","0012215"
> "0080095","myofibrillar myopathy 4","mondo","0012277"
> "0080096","myofibrillar myopathy 5","mondo","0012289"
> "0080097","myofibrillar myopathy 6","mondo","0013061"
> "0080090","reducing body myopathy","mondo","0019948"
> "0080091","spheroid body myopathy","mondo","0008448"
> "0080092","myofibrillar myopathy 1","icd10cm","G71.0"
> "0080092","myofibrillar myopathy 1","mondo","0011076"
> "0080093","myofibrillar myopathy 2","mondo","0012130"
> "12397","entropion","icd9cm","374.00"
> "12397","entropion","mesh","D004774"
> "12397","entropion","umls","C0014390"
> "12397","entropion","mondo","0001519"
> "12395","spastic entropion","icd9cm","374.03"
> "12395","spastic entropion","umls","C0155190"
> "12395","spastic entropion","mondo","0001518"
> "0080098","myofibrillar myopathy 7","mondo","0014922"
> "9088","parapsoriasis","icd10cm","L41"
> "9088","parapsoriasis","icd10cm","L41.9"
> "9088","parapsoriasis","icd9cm","696.2"
> "9088","parapsoriasis","mesh","D010267"
> "9088","parapsoriasis","umls","C0030491"
> "9088","parapsoriasis","mondo","0006592"
> "9087","anal carcinoma in situ","icd9cm","230.6"
> "9087","anal carcinoma in situ","umls","C0154064"
> "9087","anal carcinoma in situ","mondo","0004707"
> "9080","macroglobulinemia","icd10cm","C88.0"
> "9080","macroglobulinemia","icd9cm","273.3"
> "9080","macroglobulinemia","mesh","D008258"
> "9080","macroglobulinemia","umls","C0024419"
> "9080","macroglobulinemia","umls","C2936755"
> "9080","macroglobulinemia","mondo","0005190"
> "0050604","acrocapitofemoral dysplasia","mesh","C564334"
> "0050604","acrocapitofemoral dysplasia","mondo","0011907"
> "0050605","acrodermatitis enteropathica","mondo","0008713"
> "0050606","acrokeratosis verruciformis","mondo","0007048"
> "0050600","ABCD syndrome","mondo","0010895"
> "0050601","ADULT syndrome","mondo","0007072"
> "0050602","triple-A syndrome","mondo","0009279"
> "0050603","acheiropody","mondo","0008700"
> "3508","stricture or kinking of ureter","icd9cm","593.3"
> "3508","stricture or kinking of ureter","umls","C0156261"
> "3508","stricture or kinking of ureter","mondo","0002674"
> "5088","mixed epithelial stromal tumour","umls","C1334602"
> "5088","mixed epithelial stromal tumour","mondo","0003272"
> "5083","iodine hypothyroidism","icd9cm","244.2"
> "5083","iodine hypothyroidism","umls","C0154159"
> "5083","iodine hypothyroidism","mondo","0003271"
> "5082","liver cirrhosis","icd10cm","K74.60"
> "5082","liver cirrhosis","mesh","D008103"
> "5082","liver cirrhosis","umls","C0023890"
> "5082","liver cirrhosis","mondo","0005155"
> "3502","ampulla of Vater adenocarcinoma","umls","C1332243"
> "3502","ampulla of Vater adenocarcinoma","mondo","0002670"
> "3503","breast signet ring cell adenocarcinoma","umls","C1335964"
> "3503","breast signet ring cell adenocarcinoma","mondo","0002671"
> "3504","prostate signet ring cell adenocarcinoma","umls","C1335520"
> "3504","prostate signet ring cell adenocarcinoma","mondo","0002672"
> "3507","dermatofibrosarcoma protuberans","mesh","D018223"
> "3507","dermatofibrosarcoma protuberans","umls","C0206647"
> "3507","dermatofibrosarcoma protuberans","mondo","0011934"
> "2671","transitional cell carcinoma","mesh","D002295"
> "2671","transitional cell carcinoma","umls","C0007138"
> "2671","transitional cell carcinoma","umls","C0334265"
> "2671","transitional cell carcinoma","mondo","0006474"
> "2670","transitional papilloma","umls","C0334266"
> "2670","transitional papilloma","mondo","0005605"
> "0111336","craniofacial-deafness-hand syndrome","mesh","C536453"
> "0111336","craniofacial-deafness-hand syndrome","umls","C1852510"
> "0111337","Jackson-Weiss syndrome","mesh","C537559"
> "0111337","Jackson-Weiss syndrome","umls","C0795998"
> "2679","dysembryoplastic neuroepithelial tumor","umls","C1266177"
> "2679","dysembryoplastic neuroepithelial tumor","mondo","0005505"
> "2678","adult mesoblastic nephroma","umls","C1272677"
> "2678","adult mesoblastic nephroma","mondo","0002386"
> "12475","pes anserinus tendinitis or bursitis","icd9cm","726.61"
> "12475","pes anserinus tendinitis or bursitis","umls","C0158314"
> "12475","pes anserinus tendinitis or bursitis","mondo","0001533"
> "0111339","Vohwinkel syndrome","umls","C0265964"
> "2929","Newcastle disease","mesh","D009521"
> "2929","Newcastle disease","umls","C0027983"
> "2929","Newcastle disease","mondo","0005875"
> "0110310","hypertrophic cardiomyopathy 4","mondo","0007268"
> "0110313","hypertrophic cardiomyopathy 7","mondo","0013369"
> "0110312","hypertrophic cardiomyopathy 6","mondo","0010946"
> "0110315","hypertrophic cardiomyopathy 9","mondo","0013412"
> "0110314","hypertrophic cardiomyopathy 8","mondo","0012111"
> "0110317","hypertrophic cardiomyopathy 11","mondo","0012799"
> "0110316","hypertrophic cardiomyopathy 10","mondo","0012112"
> "2921","glomerulonephritis","icd10cm","N05"
> "2921","glomerulonephritis","icd10cm","N08"
> "2921","glomerulonephritis","mesh","D005921"
> "2921","glomerulonephritis","umls","C0017658"
> "2921","glomerulonephritis","mondo","0002462"
> "2920","membranoproliferative glomerulonephritis","mesh","D015432"
> "2920","membranoproliferative glomerulonephritis","umls","C0017662"
> "2920","membranoproliferative glomerulonephritis","mondo","0002461"
> "2926","Klippel-Trenaunay syndrome","icd10cm","Q87.2"
> "2926","Klippel-Trenaunay syndrome","mesh","D007715"
> "2926","Klippel-Trenaunay syndrome","umls","C0022739"
> "2926","Klippel-Trenaunay syndrome","mondo","0007864"
> "5331","testicular granulosa cell tumor","umls","C1336709"
> "5331","testicular granulosa cell tumor","mondo","0003395"
> "5330","dental pulp disease","mesh","D003788"
> "5330","dental pulp disease","umls","C0011405"
> "5330","dental pulp disease","mondo","0003394"
> "5334","paraphimosis","icd10cm","N47.2"
> "5334","paraphimosis","mesh","D010263"
> "5334","paraphimosis","umls","C0030483"
> "5334","paraphimosis","mondo","0006889"
> "5337","epulis","mesh","D005882"
> "5337","epulis","umls","C0266919"
> "5337","epulis","mondo","0003396"
> "5339","cyclic hematopoiesis","icd10cm","D70.4"
> "5339","cyclic hematopoiesis","icd9cm","288.02"
> "5339","cyclic hematopoiesis","mesh","C536227"
> "5339","cyclic hematopoiesis","umls","C0221023"
> "5339","cyclic hematopoiesis","mondo","0008090"
> "5338","gingival hypertrophy","mesh","D005886"
> "5338","gingival hypertrophy","umls","C0017567"
> "5338","gingival hypertrophy","mondo","0003397"
> "13042","persistent fetal circulation syndrome","icd10cm","P29.3"
> "13042","persistent fetal circulation syndrome","icd10cm","P29.30"
> "13042","persistent fetal circulation syndrome","icd9cm","747.83"
> "13042","persistent fetal circulation syndrome","mesh","D010547"
> "13042","persistent fetal circulation syndrome","umls","C0031190"
> "13042","persistent fetal circulation syndrome","mondo","0009934"
> "13046","acute sphenoidal sinusitis","icd10cm","J01.3"
> "13046","acute sphenoidal sinusitis","icd10cm","J01.30"
> "13046","acute sphenoidal sinusitis","icd9cm","461.3"
> "13046","acute sphenoidal sinusitis","umls","C0155807"
> "13046","acute sphenoidal sinusitis","mondo","0001624"
> "3179","inverted papilloma","mesh","D018308"
> "3179","inverted papilloma","umls","C0206721"
> "3179","inverted papilloma","mondo","0002537"
> "3178","skin papilloma","umls","C0347390"
> "3178","skin papilloma","mondo","0002536"
> "3173","fallopian tube serous papilloma","umls","C1517123"
> "3173","fallopian tube serous papilloma","mondo","0002534"
> "3172","papillary adenoma","mesh","D000236"
> "3172","papillary adenoma","umls","C0205650"
> "3172","papillary adenoma","mondo","0002533"
> "3177","verrucous papilloma","umls","C0334243"
> "3177","verrucous papilloma","mondo","0002535"
> "11258","cat-scratch disease","icd10cm","A28.1"
> "11258","cat-scratch disease","icd9cm","078.3"
> "11258","cat-scratch disease","mesh","D002372"
> "11258","cat-scratch disease","umls","C0007361"
> "11258","cat-scratch disease","mondo","0005692"
> "727","premenstrual tension","icd10cm","N94.3"
> "727","premenstrual tension","icd9cm","625.4"
> "727","premenstrual tension","mesh","D011293"
> "727","premenstrual tension","umls","C0376356"
> "727","premenstrual tension","mondo","0004169"
> "724","female stress incontinence","icd9cm","625.6"
> "724","female stress incontinence","umls","C0038437"
> "724","female stress incontinence","mondo","0004160"
> "720","normocytic anemia","umls","C0085577"
> "720","normocytic anemia","mondo","0004139"
> "728","nodular episcleritis","icd10cm","H15.12"
> "728","nodular episcleritis","icd9cm","379.02"
> "728","nodular episcleritis","umls","C0155352"
> "728","nodular episcleritis","mondo","0004170"
> "1166","palindromic rheumatism","icd10cm","M12.3"
> "1166","palindromic rheumatism","icd10cm","M12.30"
> "1166","palindromic rheumatism","icd9cm","719.3"
> "1166","palindromic rheumatism","icd9cm","719.30"
> "1166","palindromic rheumatism","icd9cm","719.31"
> "1166","palindromic rheumatism","mesh","C538103"
> "1166","palindromic rheumatism","umls","C0085574"
> "1166","palindromic rheumatism","umls","C0158178"
> "1166","palindromic rheumatism","mondo","0001332"
> "1168","familial hyperlipidemia","icd10cm","E78.5"
> "1168","familial hyperlipidemia","mesh","D006949"
> "1168","familial hyperlipidemia","mesh","D006951"
> "1168","familial hyperlipidemia","umls","C0020473"
> "1168","familial hyperlipidemia","umls","C0020476"
> "1168","familial hyperlipidemia","mondo","0001336"
> "3197","schwannoma of twelfth cranial nerve","umls","C1335928"
> "3197","schwannoma of twelfth cranial nerve","mondo","0002549"
> "11678","onchocerciasis","icd10cm","B73"
> "11678","onchocerciasis","icd9cm","125.3"
> "11678","onchocerciasis","mesh","D009855"
> "11678","onchocerciasis","umls","C0029001"
> "11678","onchocerciasis","mondo","0017137"
> "1364","ethmoidal sinus neoplasm","umls","C0345668"
> "1364","ethmoidal sinus neoplasm","mondo","0001764"
> "3193","peripheral nerve sheath neoplasm","mesh","D018317"
> "3193","peripheral nerve sheath neoplasm","umls","C0751689"
> "3193","peripheral nerve sheath neoplasm","mondo","0002547"
> "3192","neurilemmoma","mesh","D009442"
> "3192","neurilemmoma","umls","C0027809"
> "3192","neurilemmoma","mondo","0002546"
> "3191","nemaline myopathy","icd10cm","G71.2"
> "3191","nemaline myopathy","mesh","D017696"
> "3191","nemaline myopathy","umls","C0206157"
> "3191","nemaline myopathy","mondo","0018958"
> "5253","conventional leiomyosarcoma","umls","C1333157"
> "5253","conventional leiomyosarcoma","mondo","0003348"
> "1381","Fox-Fordyce disease","icd10cm","L75.2"
> "1381","Fox-Fordyce disease","icd9cm","705.82"
> "1381","Fox-Fordyce disease","mesh","D005588"
> "1381","Fox-Fordyce disease","umls","C0016632"
> "1381","Fox-Fordyce disease","mondo","0006553"
> "8552","chronic myeloid leukemia","kegg","05220"
> "8552","chronic myeloid leukemia","icd9cm","205.1"
> "8552","chronic myeloid leukemia","mesh","D015464"
> "8552","chronic myeloid leukemia","umls","C0023473"
> "8552","chronic myeloid leukemia","mondo","0011996"
> "8553","pyoderma gangrenosum","icd10cm","L88"
> "8553","pyoderma gangrenosum","icd9cm","686.01"
> "8553","pyoderma gangrenosum","mesh","D017511"
> "8553","pyoderma gangrenosum","umls","C0085652"
> "8553","pyoderma gangrenosum","mondo","0018824"
> "12804","mucopolysaccharidosis IV","icd10cm","E76.210"
> "12804","mucopolysaccharidosis IV","icd10cm","E76.219"
> "12804","mucopolysaccharidosis IV","mesh","D009085"
> "12804","mucopolysaccharidosis IV","umls","C0026707"
> "12804","mucopolysaccharidosis IV","mondo","0018938"
> "14199","posterior dislocation of lens","icd10cm","H27.13"
> "14199","posterior dislocation of lens","icd9cm","379.34"
> "14199","posterior dislocation of lens","umls","C0155373"
> "14199","posterior dislocation of lens","mondo","0001906"
> "8556","vallecula cancer","icd10cm","C10.0"
> "8556","vallecula cancer","icd9cm","146.3"
> "8556","vallecula cancer","umls","C0153386"
> "8556","vallecula cancer","mondo","0004607"
> "8557","oropharynx cancer","icd10cm","C10"
> "8557","oropharynx cancer","icd10cm","C10.2"
> "8557","oropharynx cancer","icd10cm","C10.3"
> "8557","oropharynx cancer","icd10cm","C10.8"
> "8557","oropharynx cancer","icd10cm","C10.9"
> "8557","oropharynx cancer","icd9cm","146"
> "8557","oropharynx cancer","icd9cm","146.5"
> "8557","oropharynx cancer","icd9cm","146.6"
> "8557","oropharynx cancer","icd9cm","146.7"
> "8557","oropharynx cancer","icd9cm","146.9"
> "8557","oropharynx cancer","umls","C0153382"
> "8557","oropharynx cancer","umls","C0153388"
> "8557","oropharynx cancer","umls","C0153389"
> "8557","oropharynx cancer","umls","C0153390"
> "8557","oropharynx cancer","mondo","0004608"
> "12556","acute kidney tubular necrosis","icd10cm","N17.0"
> "12556","acute kidney tubular necrosis","mesh","D007683"
> "12556","acute kidney tubular necrosis","umls","C0022672"
> "12556","acute kidney tubular necrosis","mondo","0006637"
> "12557","Duane retraction syndrome","icd10cm","H50.81"
> "12557","Duane retraction syndrome","icd9cm","378.71"
> "12557","Duane retraction syndrome","mesh","D004370"
> "12557","Duane retraction syndrome","umls","C0013261"
> "12557","Duane retraction syndrome","mondo","0007473"
> "12558","chronic progressive external ophthalmoplegia","icd10cm","H49.4"
> "12558","chronic progressive external ophthalmoplegia","icd9cm","378.72"
> "12558","chronic progressive external ophthalmoplegia","mesh","D017246"
> "12558","chronic progressive external ophthalmoplegia","umls","C0162674"
> "12558","chronic progressive external ophthalmoplegia","mondo","0005181"
> "12559","idiopathic juvenile osteoporosis","icd9cm","733.02"
> "12559","idiopathic juvenile osteoporosis","umls","C0158447"
> "12559","idiopathic juvenile osteoporosis","mondo","0019409"
> "8006","skin meningioma","umls","C1335481"
> "8006","skin meningioma","mondo","0004429"
> "8007","Pancoast tumor","mesh","D010178"
> "8007","Pancoast tumor","umls","C0030271"
> "8007","Pancoast tumor","umls","C0549471"
> "8007","Pancoast tumor","umls","C1335574"
> "8007","Pancoast tumor","mondo","0006883"
> "8000","frontal convexity meningioma","umls","C1333643"
> "8000","frontal convexity meningioma","mondo","0004426"
> "8002","supraglottis neoplasm","umls","C0345726"
> "8002","supraglottis neoplasm","mondo","0004427"
> "8003","alveoli adenoma","umls","C0334303"
> "8003","alveoli adenoma","mondo","0004428"
> "9383","iridocyclitis","icd10cm","H20.01"
> "9383","iridocyclitis","icd9cm","364.01"
> "9383","iridocyclitis","icd9cm","364.2"
> "9383","iridocyclitis","mesh","D015863"
> "9383","iridocyclitis","umls","C0007832"
> "9383","iridocyclitis","umls","C0154909"
> "9383","iridocyclitis","mondo","0004773"
> "1863","skull cancer","mesh","D012888"
> "1863","skull cancer","umls","C0037305"
> "1863","skull cancer","mondo","0002132"
> "0060000","infective endocarditis","mondo","0000565"
> "1862","jaw cancer","mesh","D007573"
> "1862","jaw cancer","umls","C0022364"
> "1862","jaw cancer","mondo","0002131"
> "0060009","MHC class I deficiency","mondo","0011476"
> "0060008","janus kinase-3 deficiency","mondo","0005511"
> "7461","large cell keratinizing variant squamous cell breast carcinoma","umls","C1519486"
> "7461","large cell keratinizing variant squamous cell breast carcinoma","mondo","0004232"
> "7460","spindle cell variant squamous cell breast carcinoma","umls","C1519487"
> "7460","spindle cell variant squamous cell breast carcinoma","mondo","0004231"
> "7465","chronic NK-cell lymphocytosis","umls","C1512709"
> "7465","chronic NK-cell lymphocytosis","mondo","0004234"
> "1866","giant cell reparative granuloma","icd10cm","M27.1"
> "1866","giant cell reparative granuloma","icd9cm","526.3"
> "1866","giant cell reparative granuloma","mesh","D006101"
> "1866","giant cell reparative granuloma","umls","C0162375"
> "1866","giant cell reparative granuloma","mondo","0006770"
> "2917","cryoglobulinemia","icd10cm","D89.1"
> "2917","cryoglobulinemia","mesh","D003449"
> "2917","cryoglobulinemia","umls","C0010403"
> "2917","cryoglobulinemia","mondo","0005576"
> "0110434","dilated cardiomyopathy 1Z","icd10cm","I42.0"
> "0110434","dilated cardiomyopathy 1Z","mondo","0012745"
> "0110435","dilated cardiomyopathy 1GG","icd10cm","I42.0"
> "0110435","dilated cardiomyopathy 1GG","mondo","0013339"
> "0110436","dilated cardiomyopathy 1L","icd10cm","I42.0"
> "0110436","dilated cardiomyopathy 1L","mondo","0011702"
> "0110437","dilated cardiomyopathy 1K","icd10cm","I42.0"
> "0110437","dilated cardiomyopathy 1K","mondo","0011567"
> "3722","solitary osseous plasmacytoma","umls","C0272256"
> "3722","solitary osseous plasmacytoma","mondo","0002755"
> "0110430","dilated cardiomyopathy 1G","icd10cm","I42.0"
> "0110430","dilated cardiomyopathy 1G","mondo","0011400"
> "0110431","dilated cardiomyopathy 1I","icd10cm","I42.0"
> "0110431","dilated cardiomyopathy 1I","mondo","0011482"
> "4686","mucoepidermoid esophageal carcinoma","umls","C1333461"
> "4686","mucoepidermoid esophageal carcinoma","mondo","0003093"
> "0110432","dilated cardiomyopathy 1NN","icd10cm","I42.0"
> "0110432","dilated cardiomyopathy 1NN","mondo","0014396"
> "4687","thyroid gland mucoepidermoid carcinoma","umls","C1513721"
> "4687","thyroid gland mucoepidermoid carcinoma","mondo","0006463"
> "0110433","dilated cardiomyopathy 1E","icd10cm","I42.0"
> "0110433","dilated cardiomyopathy 1E","mondo","0011003"
> "0080249","erythrokeratodermia variabilis et progressiva 3","mondo","0033013"
> "0080248","erythrokeratodermia variabilis et progressiva 2","mondo","0033012"
> "4685","lacrimal gland mucoepidermoid carcinoma","umls","C1334359"
> "4685","lacrimal gland mucoepidermoid carcinoma","mondo","0003092"
> "0080241","syndromic X-linked mental retardation 35","mondo","0030908"
> "4682","extrahepatic bile duct carcinoma","umls","C0238019"
> "4682","extrahepatic bile duct carcinoma","mondo","0003090"
> "0080243","amelogenesis imperfecta type 3B","mondo","0021547"
> "0080242","syndromic X-linked mental retardation Hough type","mondo","0030909"
> "0080245","Galloway-Mowat syndrome 3","mondo","0033007"
> "0080244","Galloway-Mowat syndrome 2","mondo","0033006"
> "0080247","Galloway-Mowat syndrome 5","mondo","0033009"
> "0080246","Galloway-Mowat syndrome 4","mondo","0033008"
> "13603","obstructive jaundice","mesh","D041781"
> "13603","obstructive jaundice","umls","C0022354"
> "13603","obstructive jaundice","mondo","0006874"
> "4730","vasomotor rhinitis","icd10cm","J30.0"
> "4730","vasomotor rhinitis","mesh","D012223"
> "4730","vasomotor rhinitis","umls","C0035460"
> "4730","vasomotor rhinitis","mondo","0006004"
> "4731","atrophic rhinitis","mesh","D012222"
> "4731","atrophic rhinitis","umls","C0035459"
> "4731","atrophic rhinitis","mondo","0005659"
> "4737","somatoform disorder","icd10cm","F45"
> "4737","somatoform disorder","icd10cm","F45.0"
> "4737","somatoform disorder","icd10cm","F45.9"
> "4737","somatoform disorder","icd9cm","300.8"
> "4737","somatoform disorder","icd9cm","300.81"
> "4737","somatoform disorder","mesh","D013001"
> "4737","somatoform disorder","umls","C0037650"
> "4737","somatoform disorder","umls","C0520482"
> "4737","somatoform disorder","mondo","0003117"
> "4734","calciphylaxis","mesh","D002115"
> "4734","calciphylaxis","umls","C0006666"
> "4734","calciphylaxis","mondo","0017215"
> "2316","brain ischemia","mesh","D002545"
> "2316","brain ischemia","umls","C0007786"
> "2316","brain ischemia","mondo","0005299"
> "2314","malt worker's lung","icd10cm","J67.4"
> "2314","malt worker's lung","icd9cm","495.4"
> "2314","malt worker's lung","umls","C0155888"
> "2314","malt worker's lung","mondo","0002266"
> "4739","testicular Brenner tumor","umls","C1515281"
> "4739","testicular Brenner tumor","mondo","0003118"
> "2312","nocardiosis","icd10cm","A43"
> "2312","nocardiosis","icd10cm","A43.9"
> "2312","nocardiosis","mesh","D009617"
> "2312","nocardiosis","umls","C0028242"
> "2312","nocardiosis","mondo","0017776"
> "5854","silent myocardial infarction","umls","C0340324"
> "5854","silent myocardial infarction","mondo","0003678"
> "5855","anteroseptal myocardial infarction","mesh","D056988"
> "5855","anteroseptal myocardial infarction","umls","C0262565"
> "5855","anteroseptal myocardial infarction","mondo","0003679"
> "5850","inferior myocardial infarction","mesh","D056989"
> "5850","inferior myocardial infarction","umls","C0340305"
> "5850","inferior myocardial infarction","mondo","0006803"
> "5851","posterolateral myocardial infarction","umls","C3642463"
> "5851","posterolateral myocardial infarction","mondo","0003675"
> "5852","inferolateral myocardial infarct","umls","C3537017"
> "5852","inferolateral myocardial infarct","mondo","0003676"
> "5853","lateral myocardial infarction","umls","C0340312"
> "5853","lateral myocardial infarction","mondo","0003677"
> "0110717","Warburg micro syndrome 2","icd10cm","Q87.0"
> "0110717","Warburg micro syndrome 2","mondo","0013641"
> "13732","panophthalmitis","icd9cm","360.02"
> "13732","panophthalmitis","mesh","D010202"
> "13732","panophthalmitis","umls","C0030332"
> "13732","panophthalmitis","mondo","0006884"
> "0110711","congenital hypotrichosis with juvenile macular dystrophy","mondo","0011107"
> "0110862","congenital stationary night blindness autosomal dominant 1","mondo","0012498"
> "13544","low tension glaucoma","icd10cm","H40.12"
> "13544","low tension glaucoma","icd9cm","365.12"
> "13544","low tension glaucoma","mesh","D057066"
> "13544","low tension glaucoma","umls","C0152136"
> "13544","low tension glaucoma","mondo","0006837"
> "4656","extraocular retinoblastoma","umls","C0278719"
> "4656","extraocular retinoblastoma","mondo","0003078"
> "4651","unilateral retinoblastoma","umls","C0854915"
> "4651","unilateral retinoblastoma","mondo","0003076"
> "4650","bilateral retinoblastoma","umls","C0854914"
> "4650","bilateral retinoblastoma","mondo","0003075"
> "4653","intraocular retinoblastoma","umls","C0278717"
> "4653","intraocular retinoblastoma","mondo","0003077"
> "13543","hyperparathyroidism","icd10cm","E21.3"
> "13543","hyperparathyroidism","icd9cm","252.0"
> "13543","hyperparathyroidism","icd9cm","252.00"
> "13543","hyperparathyroidism","mesh","D006961"
> "13543","hyperparathyroidism","umls","C0020502"
> "13543","hyperparathyroidism","mondo","0001741"
> "0110712","Oguchi disease-1","mondo","0009775"
> "4659","extracutaneous mastocytoma","icd10cm","D47.09"
> "4659","extracutaneous mastocytoma","mesh","D034801"
> "4659","extracutaneous mastocytoma","umls","C0272202"
> "4659","extracutaneous mastocytoma","mondo","0019025"
> "4658","benign mastocytoma","icd10cm","D47.09"
> "4658","benign mastocytoma","umls","C0024897"
> "4658","benign mastocytoma","mondo","0021048"
> "13739","nutmeg liver","icd10cm","K76.1"
> "13739","nutmeg liver","icd9cm","573.0"
> "13739","nutmeg liver","umls","C0156195"
> "13739","nutmeg liver","mondo","0001788"
> "7880","luteoma","mesh","D018311"
> "7880","luteoma","umls","C1517842"
> "7880","luteoma","mondo","0004387"
> "11760","Kohler's disease","icd9cm","732.5"
> "11760","Kohler's disease","umls","C0158444"
> "11760","Kohler's disease","mondo","0016086"
> "13738","hepatic infarction","icd10cm","K76.3"
> "13738","hepatic infarction","icd9cm","573.4"
> "13738","hepatic infarction","umls","C0151731"
> "13738","hepatic infarction","mondo","0001787"
> "11766","blind hypotensive eye","icd9cm","360.41"
> "11766","blind hypotensive eye","umls","C0154788"
> "11766","blind hypotensive eye","mondo","0001360"
> "100","intestinal infectious disease","icd10cm","A00-A09"
> "100","intestinal infectious disease","icd9cm","001-009.99"
> "100","intestinal infectious disease","umls","C0178238"
> "100","intestinal infectious disease","mondo","0000916"
> "106","pleural tuberculosis","icd10cm","A15.6"
> "106","pleural tuberculosis","icd9cm","010.1"
> "106","pleural tuberculosis","icd9cm","012.0"
> "106","pleural tuberculosis","icd9cm","012.00"
> "106","pleural tuberculosis","mesh","D014396"
> "106","pleural tuberculosis","umls","C0041326"
> "106","pleural tuberculosis","umls","C0152531"
> "106","pleural tuberculosis","mondo","0005922"
> "104","bacterial infectious disease","icd10cm","A49"
> "104","bacterial infectious disease","icd10cm","A49.9"
> "104","bacterial infectious disease","mesh","D001424"
> "104","bacterial infectious disease","umls","C0004623"
> "104","bacterial infectious disease","mondo","0005113"
> "14336","estrogen excess","icd10cm","E28.0"
> "14336","estrogen excess","icd9cm","256.0"
> "14336","estrogen excess","umls","C0154209"
> "14336","estrogen excess","mondo","0001946"
> "14443","cholinergic urticaria","icd10cm","L50.5"
> "14443","cholinergic urticaria","icd9cm","708.5"
> "14443","cholinergic urticaria","umls","C0152230"
> "14443","cholinergic urticaria","mondo","0006534"
> "14444","sclerosing keratitis","icd10cm","H16.33"
> "14444","sclerosing keratitis","icd9cm","370.54"
> "14444","sclerosing keratitis","umls","C0155090"
> "14444","sclerosing keratitis","mondo","0001965"
> "14445","chronic closed-angle glaucoma","icd10cm","H40.22"
> "14445","chronic closed-angle glaucoma","icd9cm","365.23"
> "14445","chronic closed-angle glaucoma","umls","C0154947"
> "14445","chronic closed-angle glaucoma","mondo","0001966"
> "14330","Parkinson's disease","kegg","05012"
> "14330","Parkinson's disease","icd10cm","G20"
> "14330","Parkinson's disease","icd9cm","332"
> "14330","Parkinson's disease","icd9cm","332.0"
> "14330","Parkinson's disease","mesh","D010300"
> "14330","Parkinson's disease","umls","C0030567"
> "14330","Parkinson's disease","mondo","0005180"
> "10383","amyotrophic neuralgia","icd10cm","G54.5"
> "10383","amyotrophic neuralgia","icd9cm","353.5"
> "10383","amyotrophic neuralgia","mesh","D020968"
> "10383","amyotrophic neuralgia","umls","C1510479"
> "10383","amyotrophic neuralgia","mondo","0008076"
> "14449","mixed gonadal dysgenesis","mesh","D006060"
> "14449","mixed gonadal dysgenesis","umls","C0018055"
> "14449","mixed gonadal dysgenesis","mondo","0001969"
> "0110126","Bardet-Biedl syndrome 4","icd10cm","Q87.89"
> "0110126","Bardet-Biedl syndrome 4","mondo","0014433"
> "0110127","Bardet-Biedl syndrome 5","icd10cm","Q87.89"
> "0110127","Bardet-Biedl syndrome 5","mondo","0014434"
> "0110124","Bardet-Biedl syndrome 2","icd10cm","Q87.89"
> "0110124","Bardet-Biedl syndrome 2","mondo","0014432"
> "0110125","Bardet-Biedl syndrome 3","icd10cm","Q87.89"
> "0110125","Bardet-Biedl syndrome 3","mondo","0010832"
> "7269","cribriform variant testicular seminoma","umls","C1515292"
> "7269","cribriform variant testicular seminoma","mondo","0004168"
> "0110123","Bardet-Biedl syndrome 1","icd10cm","Q87.89"
> "0110123","Bardet-Biedl syndrome 1","mondo","0008854"
> "0110120","Axenfeld-Rieger syndrome type 1","icd10cm","Q13.8"
> "0110120","Axenfeld-Rieger syndrome type 1","mondo","0008386"
> "7516","childhood central nervous system mixed germ cell tumor","umls","C1332956"
> "7516","childhood central nervous system mixed germ cell tumor","mondo","0004257"
> "7267","lung clear cell carcinoma","umls","C0345959"
> "7267","lung clear cell carcinoma","mondo","0004167"
> "7266","familiar fallopian tube carcinoma","umls","C1512418"
> "7266","familiar fallopian tube carcinoma","mondo","0004166"
> "7263","selective IgD deficiency disease","umls","C0398695"
> "7263","selective IgD deficiency disease","mondo","0004165"
> "0110129","Bardet-Biedl syndrome 7","icd10cm","Q87.89"
> "0110129","Bardet-Biedl syndrome 7","mondo","0014435"
> "6204","follicular adenoma","mesh","D000236"
> "6204","follicular adenoma","umls","C0205647"
> "6204","follicular adenoma","mondo","0005032"
> "12234","cascade stomach","icd10cm","K31.2"
> "12234","cascade stomach","icd9cm","537.6"
> "12234","cascade stomach","umls","C0267183"
> "12234","cascade stomach","mondo","0001469"
> "12237","bile reflux","mesh","D001655"
> "12237","bile reflux","umls","C0005403"
> "12237","bile reflux","mondo","0006677"
> "12236","primary biliary cirrhosis","icd10cm","K74.3"
> "12236","primary biliary cirrhosis","icd10cm","K74.5"
> "12236","primary biliary cirrhosis","icd9cm","571.6"
> "12236","primary biliary cirrhosis","mesh","D008105"
> "12236","primary biliary cirrhosis","umls","C0008312"
> "12236","primary biliary cirrhosis","umls","C0023892"
> "12236","primary biliary cirrhosis","mondo","0005388"
> "6201","pericardial mesothelioma","icd10cm","C45.2"
> "6201","pericardial mesothelioma","umls","C0346110"
> "6201","pericardial mesothelioma","umls","C0854883"
> "6201","pericardial mesothelioma","umls","C1335381"
> "6201","pericardial mesothelioma","mondo","0003805"
> "6203","thyroid hyalinizing trabecular adenoma","umls","C1336751"
> "6203","thyroid hyalinizing trabecular adenoma","mondo","0003806"
> "6208","mediastinal osteogenic sarcoma","umls","C1334675"
> "6208","mediastinal osteogenic sarcoma","mondo","0003808"
> "6209","malignant mediastinum hemangiopericytoma","umls","C1334598"
> "6209","malignant mediastinum hemangiopericytoma","mondo","0003809"
> "7512","localized intraductal papillomatosis","umls","C1333626"
> "7512","localized intraductal papillomatosis","mondo","0004254"
> "7511","breast intraductal papillomatosis","umls","C1334247"
> "7511","breast intraductal papillomatosis","mondo","0004253"
> "6809","vaginal tubular adenoma","umls","C1519932"
> "6809","vaginal tubular adenoma","mondo","0003998"
> "6804","colon Kaposi sarcoma","umls","C1333091"
> "6804","colon Kaposi sarcoma","mondo","0003997"
> "9744","type 1 diabetes mellitus","kegg","04940"
> "9744","type 1 diabetes mellitus","icd10cm","E10"
> "9744","type 1 diabetes mellitus","mesh","D003922"
> "9744","type 1 diabetes mellitus","umls","C0011854"
> "9744","type 1 diabetes mellitus","mondo","0005147"
> "9745","perianal hematoma","icd10cm","K64.5"
> "9745","perianal hematoma","icd9cm","455.4"
> "9745","perianal hematoma","umls","C0155784"
> "9745","perianal hematoma","mondo","0004871"
> "9746","hemorrhoid","icd10cm","K64"
> "9746","hemorrhoid","icd9cm","455"
> "9746","hemorrhoid","mesh","D006484"
> "9746","hemorrhoid","umls","C0019112"
> "9746","hemorrhoid","mondo","0004872"
> "9740","postcholecystectomy syndrome","icd10cm","K91.5"
> "9740","postcholecystectomy syndrome","icd9cm","576.0"
> "9740","postcholecystectomy syndrome","mesh","D017562"
> "9740","postcholecystectomy syndrome","umls","C0152099"
> "9740","postcholecystectomy syndrome","mondo","0006916"
> "9741","biliary tract disease","icd10cm","K83.9"
> "9741","biliary tract disease","icd9cm","576.9"
> "9741","biliary tract disease","mesh","D001660"
> "9741","biliary tract disease","umls","C0005424"
> "9741","biliary tract disease","mondo","0004868"
> "9742","pelvic varices","icd10cm","I86.2"
> "9742","pelvic varices","icd9cm","456.5"
> "9742","pelvic varices","umls","C0155795"
> "9742","pelvic varices","mondo","0004869"
> "9743","diabetic neuropathy","icd9cm","250.6"
> "9743","diabetic neuropathy","mesh","D003929"
> "9743","diabetic neuropathy","umls","C0011882"
> "9743","diabetic neuropathy","mondo","0006626"
> "0060272","pontocerebellar hypoplasia type 3","mesh","C548072"
> "0060272","pontocerebellar hypoplasia type 3","umls","C1842687"
> "0060272","pontocerebellar hypoplasia type 3","mondo","0011948"
> "10568","early yaws","icd10cm","A66.0"
> "10568","early yaws","icd10cm","A66.6"
> "10568","early yaws","icd9cm","102.0"
> "10568","early yaws","icd9cm","102.6"
> "10568","early yaws","umls","C0275990"
> "10568","early yaws","umls","C0275998"
> "10568","early yaws","umls","C0343834"
> "10568","early yaws","mondo","0001067"
> "9749","internal hemorrhoid","icd9cm","455.6"
> "9749","internal hemorrhoid","umls","C0041844"
> "9749","internal hemorrhoid","mondo","0004873"
> "8838","Hodgkin's lymphoma, nodular sclerosis","icd10cm","C81.1"
> "8838","Hodgkin's lymphoma, nodular sclerosis","icd9cm","201.5"
> "8838","Hodgkin's lymphoma, nodular sclerosis","umls","C0152268"
> "8838","Hodgkin's lymphoma, nodular sclerosis","mondo","0004665"
> "1876","sexual dysfunction","icd10cm","F52.9"
> "1876","sexual dysfunction","icd10cm","R37"
> "1876","sexual dysfunction","umls","C0549622"
> "1876","sexual dysfunction","mondo","0002134"
> "0060278","pontocerebellar hypoplasia type 9","icd10cm","Q04.3"
> "0060278","pontocerebellar hypoplasia type 9","mondo","0014351"
> "7678","sphenoid sinus inverted papilloma","umls","C1336037"
> "7678","sphenoid sinus inverted papilloma","mondo","0004326"
> "7679","sphenoid sinus Schneiderian papilloma","umls","C1336038"
> "7679","sphenoid sinus Schneiderian papilloma","mondo","0004327"
> "7676","testicular thecoma","umls","C1515299"
> "7676","testicular thecoma","mondo","0004325"
> "7675","testicular fibroma","umls","C1515282"
> "7675","testicular fibroma","mondo","0004324"
> "1759","American histoplasmosis","icd10cm","B39.4"
> "1759","American histoplasmosis","icd9cm","115.0"
> "1759","American histoplasmosis","mesh","D006660"
> "1759","American histoplasmosis","umls","C0153261"
> "1759","American histoplasmosis","mondo","0002099"
> "1757","facial hemiatrophy","mesh","D005150"
> "1757","facial hemiatrophy","umls","C0015458"
> "1757","facial hemiatrophy","mondo","0007710"
> "1756","facial nerve disease","icd10cm","G51"
> "1756","facial nerve disease","icd10cm","G51.9"
> "1756","facial nerve disease","icd9cm","351"
> "1756","facial nerve disease","icd9cm","351.9"
> "1756","facial nerve disease","mesh","D005155"
> "1756","facial nerve disease","umls","C0015464"
> "1756","facial nerve disease","mondo","0002098"
> "1754","mitral valve stenosis","mesh","D008946"
> "1754","mitral valve stenosis","umls","C0026269"
> "1754","mitral valve stenosis","mondo","0005852"
> "1752","ocular melanoma","mondo","0006325"
> "1751","malignant conjunctival melanoma","umls","C0346360"
> "1751","malignant conjunctival melanoma","mondo","0002096"
> "1285","rectal disease","mesh","D012002"
> "1285","rectal disease","umls","C0034882"
> "1285","rectal disease","mondo","0001593"
> "1284","prolapse of female genital organ","icd9cm","618.8"
> "1284","prolapse of female genital organ","icd9cm","618.89"
> "1284","prolapse of female genital organ","umls","C0029801"
> "1284","prolapse of female genital organ","mondo","0001592"
> "1287","cardiovascular system disease","icd9cm","429.2"
> "1287","cardiovascular system disease","mesh","D002318"
> "1287","cardiovascular system disease","umls","C0007222"
> "1287","cardiovascular system disease","mondo","0004995"
> "11168","anogenital venereal wart","icd10cm","A63.0"
> "11168","anogenital venereal wart","icd9cm","078.11"
> "11168","anogenital venereal wart","mesh","D003218"
> "11168","anogenital venereal wart","umls","C0009663"
> "11168","anogenital venereal wart","umls","C0554632"
> "11168","anogenital venereal wart","mondo","0005647"
> "1283","enterocele","icd10cm","K46"
> "1283","enterocele","icd10cm","N81.5"
> "1283","enterocele","icd9cm","618.6"
> "1283","enterocele","mesh","D006547"
> "1283","enterocele","umls","C0205792"
> "1283","enterocele","mondo","0001589"
> "11164","band keratopathy","icd10cm","H18.42"
> "11164","band keratopathy","icd9cm","371.43"
> "11164","band keratopathy","mesh","C562399"
> "11164","band keratopathy","umls","C0155120"
> "11164","band keratopathy","mondo","0009016"
> "11165","common wart","icd10cm","B07"
> "11165","common wart","icd10cm","B07.8"
> "11165","common wart","icd9cm","078.1"
> "11165","common wart","umls","C0043037"
> "11165","common wart","mondo","0001209"
> "1289","neurodegenerative disease","icd10cm","G31.9"
> "1289","neurodegenerative disease","mesh","D019636"
> "1289","neurodegenerative disease","umls","C0524851"
> "1289","neurodegenerative disease","umls","C1285162"
> "1289","neurodegenerative disease","mondo","0005559"
> "11161","neonatal respiratory failure","icd10cm","P28.5"
> "11161","neonatal respiratory failure","icd9cm","770.84"
> "11161","neonatal respiratory failure","umls","C0521648"
> "11161","neonatal respiratory failure","mondo","0001207"
> "11162","respiratory failure","icd10cm","J96.0"
> "11162","respiratory failure","icd9cm","518.81"
> "11162","respiratory failure","umls","C0264490"
> "11162","respiratory failure","mondo","0021113"
> "1579","respiratory system disease","icd10cm","J96-J99"
> "1579","respiratory system disease","icd10cm","J98"
> "1579","respiratory system disease","icd9cm","510-519.99"
> "1579","respiratory system disease","icd9cm","519"
> "1579","respiratory system disease","umls","C0029582"
> "1579","respiratory system disease","mondo","0005087"
> "1578","pulmonary systemic sclerosis","icd10cm","M34.81"
> "1578","pulmonary systemic sclerosis","icd9cm","517.2"
> "1578","pulmonary systemic sclerosis","umls","C0339904"
> "1578","pulmonary systemic sclerosis","mondo","0002047"
> "8761","megakaryocytic leukemia","icd10cm","C94.2"
> "8761","megakaryocytic leukemia","icd10cm","C94.20"
> "8761","megakaryocytic leukemia","icd9cm","207.2"
> "8761","megakaryocytic leukemia","mesh","D007947"
> "8761","megakaryocytic leukemia","umls","C0023462"
> "8761","megakaryocytic leukemia","mondo","0018872"
> "688","embryonal cancer","mesh","D009373"
> "688","embryonal cancer","umls","C0027654"
> "688","embryonal cancer","mondo","0005564"
> "1573","communicating hydrocephalus","icd10cm","G91.0"
> "1573","communicating hydrocephalus","icd9cm","331.3"
> "1573","communicating hydrocephalus","mesh","D006849"
> "1573","communicating hydrocephalus","umls","C0009451"
> "1573","communicating hydrocephalus","mondo","0002045"
> "684","hepatocellular carcinoma","icd10cm","C22.0"
> "684","hepatocellular carcinoma","mondo","0007256"
> "687","hepatoblastoma","icd10cm","C22.2"
> "687","hepatoblastoma","mesh","D018197"
> "687","hepatoblastoma","umls","C0206624"
> "687","hepatoblastoma","mondo","0018666"
> "686","liver carcinoma","umls","C0279000"
> "686","liver carcinoma","mondo","0007256"
> "681","progressive bulbar palsy","icd10cm","G12.22"
> "681","progressive bulbar palsy","icd9cm","335.22"
> "681","progressive bulbar palsy","mesh","D010244"
> "681","progressive bulbar palsy","umls","C0030442"
> "681","progressive bulbar palsy","mondo","0008890"
> "680","tauopathy","mesh","D024801"
> "680","tauopathy","umls","C0949664"
> "680","tauopathy","mondo","0005574"
> "683","motor neuritis","mesh","D009443"
> "683","motor neuritis","umls","C0235025"
> "683","motor neuritis","mondo","0004004"
> "682","compartment syndrome","icd10cm","T79.A0"
> "682","compartment syndrome","icd9cm","958.90"
> "682","compartment syndrome","mesh","D003161"
> "682","compartment syndrome","umls","C0009492"
> "682","compartment syndrome","mondo","0004001"
> "13832","patent ductus arteriosus","icd10cm","Q25.0"
> "13832","patent ductus arteriosus","icd9cm","747.0"
> "13832","patent ductus arteriosus","mesh","D004374"
> "13832","patent ductus arteriosus","umls","C0013274"
> "13832","patent ductus arteriosus","mondo","0011827"
> "1240","leukemia","icd10cm","C95"
> "1240","leukemia","icd10cm","C95.9"
> "1240","leukemia","icd10cm","C95.90"
> "1240","leukemia","icd9cm","208"
> "1240","leukemia","icd9cm","208.9"
> "1240","leukemia","mesh","D007938"
> "1240","leukemia","umls","C0023418"
> "1240","leukemia","mondo","0005059"
> "8051","bladder papillary clear cell adenocarcinoma","umls","C1511196"
> "8051","bladder papillary clear cell adenocarcinoma","mondo","0004445"
> "8502","bullous skin disease","icd9cm","694.8"
> "8502","bullous skin disease","umls","C0079957"
> "8502","bullous skin disease","mondo","0019337"
> "8505","dermatitis herpetiformis","icd10cm","L13.0"
> "8505","dermatitis herpetiformis","icd9cm","694.0"
> "8505","dermatitis herpetiformis","mesh","D003874"
> "8505","dermatitis herpetiformis","umls","C0011608"
> "8505","dermatitis herpetiformis","mondo","0015614"
> "5629","adenosquamous colon carcinoma","umls","C1333082"
> "5629","adenosquamous colon carcinoma","mondo","0003554"
> "5628","ampulla of Vater adenosquamous carcinoma","umls","C1332245"
> "5628","ampulla of Vater adenosquamous carcinoma","mondo","0003553"
> "5627","adenosquamous gallbladder carcinoma","umls","C1333741"
> "5627","adenosquamous gallbladder carcinoma","mondo","0006217"
> "5626","thymus adenosquamous carcinoma","umls","C1332171"
> "5626","thymus adenosquamous carcinoma","mondo","0003551"
> "5625","esophageal adenosquamous carcinoma","mondo","0003550"
> "5624","adenosquamous bile duct carcinoma","umls","C0861854"
> "5624","adenosquamous bile duct carcinoma","mondo","0003549"
> "5623","adenosquamous breast carcinoma","umls","C1510796"
> "5623","adenosquamous breast carcinoma","mondo","0003548"
> "5621","histiocytic and dendritic cell cancer","umls","C1334030"
> "5621","histiocytic and dendritic cell cancer","mondo","0006247"
> "8499","night blindness","icd10cm","H53.6"
> "8499","night blindness","icd10cm","H53.60"
> "8499","night blindness","icd9cm","368.6"
> "8499","night blindness","icd9cm","368.60"
> "8499","night blindness","mesh","D009755"
> "8499","night blindness","umls","C0028077"
> "8499","night blindness","mondo","0004588"
> "8498","hereditary night blindness","icd10cm","H53.63"
> "8498","hereditary night blindness","icd9cm","368.61"
> "8498","hereditary night blindness","mesh","C537743"
> "8498","hereditary night blindness","umls","C1306122"
> "8498","hereditary night blindness","mondo","0004587"
> "0060454","subepithelial mucinous corneal dystrophy","icd10cm","H18.5"
> "0060454","subepithelial mucinous corneal dystrophy","mesh","C567547"
> "0060454","subepithelial mucinous corneal dystrophy","mondo","0013026"
> "10966","lipoid nephrosis","icd10cm","N04"
> "10966","lipoid nephrosis","mesh","D009402"
> "10966","lipoid nephrosis","umls","C0027721"
> "10966","lipoid nephrosis","mondo","0006835"
> "4184","pseudohypoparathyroidism","icd10cm","E20.1"
> "4184","pseudohypoparathyroidism","mesh","D011547"
> "4184","pseudohypoparathyroidism","umls","C0033806"
> "4184","pseudohypoparathyroidism","mondo","0019992"
> "5997","non-proliferative fibrocystic change of the breast","umls","C1332628"
> "5997","non-proliferative fibrocystic change of the breast","mondo","0003724"
> "5996","blunt duct adenosis of breast","umls","C1332573"
> "5996","blunt duct adenosis of breast","mondo","0003723"
> "5990","internal auditory canal meningioma","umls","C1334227"
> "5990","internal auditory canal meningioma","mondo","0003722"
> "11577","Cauda equina syndrome","icd10cm","G83.4"
> "11577","Cauda equina syndrome","icd9cm","344.6"
> "11577","Cauda equina syndrome","mesh","D011128"
> "11577","Cauda equina syndrome","umls","C0392548"
> "11577","Cauda equina syndrome","mondo","0005693"
> "4186","articulation disorder","mesh","D001184"
> "4186","articulation disorder","umls","C0003910"
> "4186","articulation disorder","mondo","0002903"
> "5999","apocrine adenosis of breast","umls","C1332314"
> "5999","apocrine adenosis of breast","mondo","0003726"
> "5998","microglandular adenosis","mesh","D005348"
> "5998","microglandular adenosis","umls","C0085750"
> "5998","microglandular adenosis","mondo","0003725"
> "0110867","congenital stationary night blindness 1C","mondo","0013183"
> "10247","pleurisy","icd9cm","511.8"
> "10247","pleurisy","mesh","D010998"
> "10247","pleurisy","umls","C0029799"
> "10247","pleurisy","mondo","0000986"
> "0111455","GRACILE syndrome","mesh","C537934"
> "0111455","GRACILE syndrome","umls","C1864002"
> "0090086","hypogonadotropic hypogonadism 6 with or without anosmia","icd10cm","E23.0"
> "0090086","hypogonadotropic hypogonadism 6 with or without anosmia","mondo","0012988"
> "0090087","hypogonadotropic hypogonadism 14 with or without anosmia","icd10cm","E23.0"
> "0090087","hypogonadotropic hypogonadism 14 with or without anosmia","mondo","0013926"
> "0090084","hypogonadotropic hypogonadism 5 with or without anosmia","icd10cm","E23.0"
> "0090084","hypogonadotropic hypogonadism 5 with or without anosmia","mondo","0012880"
> "0090085","hypogonadotropic hypogonadism 9 with or without anosmia","icd10cm","E23.0"
> "0090085","hypogonadotropic hypogonadism 9 with or without anosmia","mondo","0013911"
> "0090082","hypogonadotropic hypogonadism 20 with or without anosmia","icd10cm","E23.0"
> "0090082","hypogonadotropic hypogonadism 20 with or without anosmia","mondo","0014106"
> "0090083","hypogonadotropic hypogonadism 2 with or without anosmia","icd10cm","E23.0"
> "0090083","hypogonadotropic hypogonadism 2 with or without anosmia","mondo","0007844"
> "0090080","hypogonadotropic hypogonadism 16 with or without anosmia","icd10cm","E23.0"
> "0090080","hypogonadotropic hypogonadism 16 with or without anosmia","mondo","0013961"
> "0090081","hypogonadotropic hypogonadism 22 with or without anosmia","icd10cm","E23.0"
> "0090081","hypogonadotropic hypogonadism 22 with or without anosmia","mondo","0014461"
> "0090088","hypogonadotropic hypogonadism 24 without anosmia","icd10cm","E23.6"
> "0090088","hypogonadotropic hypogonadism 24 without anosmia","mondo","0009239"
> "0090089","hypogonadotropic hypogonadism 10 with or without anosmia","icd10cm","E23.0"
> "0090089","hypogonadotropic hypogonadism 10 with or without anosmia","mondo","0013912"
> "0110948","Waardenburg syndrome type 1","mesh","D014849"
> "0110948","Waardenburg syndrome type 1","umls","C1847800"
> "0110948","Waardenburg syndrome type 1","mondo","0008670"
> "0110949","Waardenburg syndrome type 3","icd10cm","E70.3"
> "0110949","Waardenburg syndrome type 3","mondo","0007862"
> "6787","childhood vagina botryoid rhabdomyosarcoma","umls","C1332945"
> "6787","childhood vagina botryoid rhabdomyosarcoma","mondo","0003993"
> "6786","childhood botryoid rhabdomyosarcoma","umls","C1332944"
> "6786","childhood botryoid rhabdomyosarcoma","mondo","0003992"
> "0110940","autosomal recessive osteopetrosis 8","mondo","0014040"
> "0110941","autosomal recessive osteopetrosis 3","mondo","0009818"
> "0110942","autosomal recessive osteopetrosis 1","mondo","0009815"
> "0110943","autosomal recessive osteopetrosis 2","mondo","0009816"
> "0110944","autosomal recessive osteopetrosis 4","mondo","0012676"
> "0110945","autosomal recessive osteopetrosis 6","mondo","0012679"
> "0110946","autosomal recessive osteopetrosis 7","icd10cm","Q78.2"
> "0110946","autosomal recessive osteopetrosis 7","mondo","0012859"
> "0110947","Waardenburg syndrome type 2B","mondo","0010841"
> "11868","chronic erythremia","icd9cm","207.1"
> "11868","chronic erythremia","umls","C0152272"
> "11868","chronic erythremia","mondo","0001394"
> "0060838","isolated microphthalmia 7","icd10cm","Q11.0"
> "0060838","isolated microphthalmia 7","mondo","0013377"
> "0060839","isolated microphthalmia 2","icd10cm","Q11.0"
> "0060839","isolated microphthalmia 2","mondo","0012409"
> "0060834","Griscelli syndrome type 3","mesh","C537303"
> "0060834","Griscelli syndrome type 3","umls","C1836573"
> "0060834","Griscelli syndrome type 3","mondo","0012220"
> "0060835","isolated microphthalmia 6","icd10cm","Q11.0"
> "0060835","isolated microphthalmia 6","mondo","0013293"
> "0060836","isolated microphthalmia 4","icd10cm","Q11.0"
> "0060836","isolated microphthalmia 4","mondo","0013130"
> "0060837","isolated microphthalmia 5","icd10cm","Q15.8"
> "0060837","isolated microphthalmia 5","mondo","0012605"
> "0060830","deafness-intellectual disability, Martin-Probst type syndrome","icd10cm","Q87.8"
> "0060830","deafness-intellectual disability, Martin-Probst type syndrome","mondo","0010353"
> "0060831","Griscelli syndrome","icd10cm","E70.3"
> "0060831","Griscelli syndrome","mondo","0018306"
> "0060832","Griscelli syndrome type 1","mesh","C537301"
> "0060832","Griscelli syndrome type 1","umls","C1859194"
> "0060832","Griscelli syndrome type 1","mondo","0008962"
> "0060833","Griscelli syndrome type 2","mesh","C537302"
> "0060833","Griscelli syndrome type 2","umls","C1868679"
> "0060833","Griscelli syndrome type 2","mondo","0011872"
> "2885","benign prostate phyllodes tumor","umls","C1332535"
> "2885","benign prostate phyllodes tumor","umls","C1335409"
> "2885","benign prostate phyllodes tumor","mondo","0002451"
> "12002","trachea sarcoma","umls","C1336774"
> "12002","trachea sarcoma","mondo","0001418"
> "12003","trachea squamous cell carcinoma","umls","C0345946"
> "12003","trachea squamous cell carcinoma","mondo","0001419"
> "12001","tracheal lymphoma","umls","C1336773"
> "12001","tracheal lymphoma","mondo","0001417"
> "1248","ocular hyperemia","umls","C0155169"
> "1248","ocular hyperemia","mondo","0001534"
> "9249","Beemer-Langer syndrome","mesh","C537599"
> "9249","Beemer-Langer syndrome","umls","C0432198"
> "9249","Beemer-Langer syndrome","mondo","0010024"
> "9248","Pallister-Hall syndrome","mesh","D054975"
> "9248","Pallister-Hall syndrome","umls","C0265220"
> "9248","Pallister-Hall syndrome","mondo","0007804"
> "0070288","primary autosomal recessive microcephaly 17","mondo","0014908"
> "2889","retrocochlear disease","mesh","D012181"
> "2889","retrocochlear disease","umls","C0035352"
> "2889","retrocochlear disease","mondo","0002453"
> "9538","multiple myeloma","icd10cm","C90.0"
> "9538","multiple myeloma","icd10cm","C90.00"
> "9538","multiple myeloma","icd9cm","203.0"
> "9538","multiple myeloma","mesh","D009101"
> "9538","multiple myeloma","umls","C0026764"
> "9538","multiple myeloma","mondo","0009693"
> "9537","Lassa fever","icd10cm","A96.2"
> "9537","Lassa fever","mesh","D007835"
> "9537","Lassa fever","umls","C0023092"
> "9537","Lassa fever","mondo","0005820"
> "9240","erythromelalgia","icd10cm","I73.81"
> "9240","erythromelalgia","icd9cm","443.82"
> "9240","erythromelalgia","mesh","D004916"
> "9240","erythromelalgia","umls","C0014804"
> "9240","erythromelalgia","mondo","0016028"
> "0070280","primary autosomal recessive microcephaly 5","mondo","0012106"
> "9534","tuberculous pneumothorax","icd10cm","A15.0"
> "9534","tuberculous pneumothorax","icd9cm","011.7"
> "9534","tuberculous pneumothorax","icd9cm","011.70"
> "9534","tuberculous pneumothorax","umls","C0152600"
> "9534","tuberculous pneumothorax","mondo","0004813"
> "9245","Alagille syndrome","icd10cm","Q44.7"
> "9245","Alagille syndrome","mesh","D016738"
> "9245","Alagille syndrome","umls","C0085280"
> "9245","Alagille syndrome","mondo","0007318"
> "0070287","primary autosomal recessive microcephaly 11","mondo","0014173"
> "0070284","primary autosomal recessive microcephaly 12","mondo","0014484"
> "9246","cerebral amyloid angiopathy","mesh","D028243"
> "9246","cerebral amyloid angiopathy","umls","C0268393"
> "9246","cerebral amyloid angiopathy","umls","C1510489"
> "9246","cerebral amyloid angiopathy","umls","C1527338"
> "9246","cerebral amyloid angiopathy","umls","C1956349"
> "9246","cerebral amyloid angiopathy","mondo","0005620"
> "1555","urticaria","icd9cm","708.8"
> "1555","urticaria","mesh","D014581"
> "1555","urticaria","umls","C0029839"
> "1555","urticaria","mondo","0005492"
> "3698","bile duct mucinous adenocarcinoma","umls","C0861856"
> "3698","bile duct mucinous adenocarcinoma","mondo","0002739"
> "3699","uterine ligament mucinous adenocarcinoma","umls","C1519869"
> "3699","uterine ligament mucinous adenocarcinoma","mondo","0002740"
> "3690","brachial plexus neuropathy","icd10cm","G54.0"
> "3690","brachial plexus neuropathy","mesh","D020516"
> "3690","brachial plexus neuropathy","umls","C0700251"
> "3690","brachial plexus neuropathy","mondo","0006683"
> "3691","anal colloid adenocarcinoma","umls","C1332272"
> "3691","anal colloid adenocarcinoma","mondo","0002734"
> "3692","anal canal adenocarcinoma","umls","C1332259"
> "3692","anal canal adenocarcinoma","mondo","0002735"
> "3693","ampulla of Vater mucinous adenocarcinoma","umls","C1332248"
> "3693","ampulla of Vater mucinous adenocarcinoma","mondo","0002736"
> "3696","acute sanguinous otitis media","icd9cm","381.03"
> "3696","acute sanguinous otitis media","umls","C0395865"
> "3696","acute sanguinous otitis media","mondo","0002737"
> "3697","acute transudative otitis media","icd9cm","381.0"
> "3697","acute transudative otitis media","icd9cm","381.00"
> "3697","acute transudative otitis media","umls","C0271432"
> "3697","acute transudative otitis media","mondo","0002738"
> "12750","cyclosporiasis","icd10cm","A07.4"
> "12750","cyclosporiasis","icd9cm","007.5"
> "12750","cyclosporiasis","mesh","D021866"
> "12750","cyclosporiasis","umls","C0343398"
> "12750","cyclosporiasis","mondo","0005725"
> "3526","cerebral infarction","icd10cm","I63"
> "3526","cerebral infarction","icd10cm","I63.9"
> "3526","cerebral infarction","mesh","D002544"
> "3526","cerebral infarction","umls","C0007785"
> "3526","cerebral infarction","mondo","0002679"
> "3527","cerebral arterial disease","mesh","D002539"
> "3527","cerebral arterial disease","umls","C0007774"
> "3527","cerebral arterial disease","mondo","0006693"
> "3525","middle cerebral artery infarction","mesh","D020244"
> "3525","middle cerebral artery infarction","umls","C0740392"
> "3525","middle cerebral artery infarction","mondo","0006857"
> "3522","lateral medullary syndrome","icd10cm","G46.3"
> "3522","lateral medullary syndrome","mesh","D014854"
> "3522","lateral medullary syndrome","umls","C0043019"
> "3522","lateral medullary syndrome","mondo","0006827"
> "3523","brain stem infarction","mesh","D020526"
> "3523","brain stem infarction","umls","C0521542"
> "3523","brain stem infarction","mondo","0006686"
> "3520","pediatric fibrosarcoma","umls","C0279981"
> "3520","pediatric fibrosarcoma","mondo","0002678"
> "0050629","Aicardi-Goutieres syndrome","icd10cm","G31.8"
> "0050629","Aicardi-Goutieres syndrome","mondo","0018866"
> "0050625","biliary tract benign neoplasm","umls","C0345913"
> "0050625","biliary tract benign neoplasm","mondo","0005304"
> "3528","anterior cerebral artery infarction","mesh","D020243"
> "3528","anterior cerebral artery infarction","umls","C0751843"
> "3528","anterior cerebral artery infarction","mondo","0006647"
> "3529","central core myopathy","icd10cm","G71.2"
> "3529","central core myopathy","mesh","D020512"
> "3529","central core myopathy","umls","C0751951"
> "3529","central core myopathy","mondo","0007294"
> "2150","ovarian lymphoma","umls","C1518720"
> "2150","ovarian lymphoma","mondo","0002227"
> "2698","nephrogenic adenofibroma","umls","C1266141"
> "2698","nephrogenic adenofibroma","mondo","0002396"
> "2697","renal adenoma","umls","C0334684"
> "2697","renal adenoma","mondo","0002395"
> "2696","Leydig cell tumor","mesh","D007984"
> "2696","Leydig cell tumor","umls","C0023601"
> "2696","Leydig cell tumor","mondo","0006266"
> "10718","giardiasis","icd10cm","A07.1"
> "10718","giardiasis","icd9cm","007.1"
> "10718","giardiasis","mesh","D005873"
> "10718","giardiasis","umls","C0017536"
> "10718","giardiasis","mondo","0001103"
> "10719","toxic diffuse goiter","icd9cm","242.00"
> "10719","toxic diffuse goiter","umls","C0154138"
> "10719","toxic diffuse goiter","mondo","0001104"
> "2691","myoma","icd10cm","D21"
> "2691","myoma","mesh","D009214"
> "2691","myoma","umls","C0027086"
> "2691","myoma","mondo","0003061"
> "0110379","retinitis pigmentosa 43","icd10cm","H35.5"
> "0110379","retinitis pigmentosa 43","mondo","0013437"
> "0110378","retinitis pigmentosa 29","icd10cm","H35.5"
> "0110378","retinitis pigmentosa 29","mondo","0012813"
> "14654","prostatitis","icd10cm","N41"
> "14654","prostatitis","icd10cm","N41.9"
> "14654","prostatitis","icd9cm","601"
> "14654","prostatitis","icd9cm","601.9"
> "14654","prostatitis","mesh","D011472"
> "14654","prostatitis","umls","C0033581"
> "14654","prostatitis","mondo","0005280"
> "0110373","retinitis pigmentosa 61","icd10cm","H35.5"
> "0110373","retinitis pigmentosa 61","mondo","0013610"
> "0110372","retinitis pigmentosa 4","icd10cm","H35.5"
> "0110372","retinitis pigmentosa 4","mondo","0013395"
> "0110371","retinitis pigmentosa 56","icd10cm","H35.5"
> "0110371","retinitis pigmentosa 56","mondo","0013314"
> "0110370","retinitis pigmentosa 55","icd10cm","H35.5"
> "0110370","retinitis pigmentosa 55","mondo","0013312"
> "0110377","retinitis pigmentosa 49","icd10cm","H35.5"
> "0110377","retinitis pigmentosa 49","mondo","0013405"
> "0110376","retinitis pigmentosa 41","icd10cm","H35.5"
> "0110376","retinitis pigmentosa 41","mondo","0012796"
> "0110375","retinitis pigmentosa 40","icd10cm","H35.5"
> "0110375","retinitis pigmentosa 40","mondo","0013429"
> "0110374","retinitis pigmentosa 68","icd10cm","H35.5"
> "0110374","retinitis pigmentosa 68","mondo","0014323"
> "1362","paranasal sinus sarcoma","umls","C1335342"
> "1362","paranasal sinus sarcoma","mondo","0001758"
> "0050742","nicotine dependence","icd10cm","F17"
> "0050742","nicotine dependence","icd10cm","F17.2"
> "0050742","nicotine dependence","icd10cm","F17.20"
> "0050742","nicotine dependence","mesh","D014029"
> "0050742","nicotine dependence","umls","C0028043"
> "0050742","nicotine dependence","mondo","0008575"
> "0060490","Schimke immuno-osseous dysplasia","mesh","C536629"
> "0060490","Schimke immuno-osseous dysplasia","umls","C0877024"
> "0060490","Schimke immuno-osseous dysplasia","mondo","0009458"
> "13060","traumatic glaucoma","icd9cm","365.65"
> "13060","traumatic glaucoma","umls","C0339594"
> "13060","traumatic glaucoma","mondo","0001626"
> "13068","renal osteodystrophy","icd10cm","N25.0"
> "13068","renal osteodystrophy","icd9cm","588.0"
> "13068","renal osteodystrophy","mesh","D012080"
> "13068","renal osteodystrophy","umls","C0035086"
> "13068","renal osteodystrophy","mondo","0006946"
> "1360","frontal sinus cancer","icd10cm","C31.2"
> "1360","frontal sinus cancer","icd9cm","160.4"
> "1360","frontal sinus cancer","umls","C0153478"
> "1360","frontal sinus cancer","mondo","0001756"
> "1142","alternating exotropia","icd10cm","H50.15"
> "1142","alternating exotropia","icd9cm","378.15"
> "1142","alternating exotropia","mesh","D005099"
> "1142","alternating exotropia","umls","C0152207"
> "1142","alternating exotropia","mondo","0001281"
> "1143","exotropia","icd10cm","H50.1"
> "1143","exotropia","icd10cm","H50.10"
> "1143","exotropia","icd9cm","378.1"
> "1143","exotropia","icd9cm","378.10"
> "1143","exotropia","mesh","D005099"
> "1143","exotropia","umls","C0015310"
> "1143","exotropia","mondo","0001286"
> "1140","spinal canal and spinal cord meningioma","umls","C1334264"
> "1140","spinal canal and spinal cord meningioma","mondo","0001279"
> "1148","polydactyly","icd10cm","Q69"
> "1148","polydactyly","icd10cm","Q69.9"
> "1148","polydactyly","icd9cm","755.0"
> "1148","polydactyly","icd9cm","755.00"
> "1148","polydactyly","mesh","C562429"
> "1148","polydactyly","mesh","D017689"
> "1148","polydactyly","umls","C0152427"
> "1148","polydactyly","umls","C0220697"
> "1148","polydactyly","mondo","0021003"
> "14491","regional ureteric cancer","umls","C0854921"
> "14491","regional ureteric cancer","mondo","0001978"
> "14759","autosomal recessive type IV Ehlers-Danlos syndrome","umls","C0268340"
> "14759","autosomal recessive type IV Ehlers-Danlos syndrome","mondo","0002014"
> "7198","maxillary sinus adenoid cystic carcinoma","umls","C1334643"
> "7198","maxillary sinus adenoid cystic carcinoma","mondo","0006297"
> "0060249","scoliosis","icd10cm","M41"
> "0060249","scoliosis","icd10cm","M41.9"
> "0060249","scoliosis","mesh","D012600"
> "0060249","scoliosis","umls","C0036439"
> "0060249","scoliosis","mondo","0005392"
> "0060248","Simpson-Golabi-Behmel syndrome type 1","mesh","C537340"
> "0060248","Simpson-Golabi-Behmel syndrome type 1","umls","C0796154"
> "0060248","Simpson-Golabi-Behmel syndrome type 1","mondo","0020602"
> "0060247","Smith-McCort dysplasia","mesh","C564589"
> "0060247","Smith-McCort dysplasia","umls","C1846431"
> "0060247","Smith-McCort dysplasia","mondo","0015799"
> "7192","hereditary conventional renal cell carcinoma","umls","C1333985"
> "7192","hereditary conventional renal cell carcinoma","mondo","0018492"
> "7191","ovarian endometrioid cystadenoma","umls","C1518713"
> "7191","ovarian endometrioid cystadenoma","mondo","0004136"
> "0060244","specific language impairment","mondo","0000724"
> "0060243","stuttering","icd10cm","F80.81"
> "0060243","stuttering","mesh","D013342"
> "0060243","stuttering","umls","C0038131"
> "0060243","stuttering","umls","C0038506"
> "0060243","stuttering","umls","C0454542"
> "0060243","stuttering","umls","C0751527"
> "0060243","stuttering","umls","C0751528"
> "0060243","stuttering","umls","C0751529"
> "0060243","stuttering","umls","C3489627"
> "0060243","stuttering","mondo","0000723"
> "0060242","synpolydactyly","mesh","C538153"
> "0060242","synpolydactyly","umls","C2699746"
> "0060242","synpolydactyly","mondo","0000722"
> "0060241","3-M syndrome","mesh","C535314"
> "0060241","3-M syndrome","mesh","C535725"
> "0060241","3-M syndrome","umls","C1848862"
> "0060241","3-M syndrome","umls","C1851996"
> "0060241","3-M syndrome","mondo","0007477"
> "0060240","UV-sensitive syndrome","mesh","C563466"
> "0060240","UV-sensitive syndrome","mondo","0015797"
> "2648","sebaceous adenoma","umls","C1368816"
> "2648","sebaceous adenoma","mondo","0002375"
> "8538","reticulosarcoma","icd9cm","200.0"
> "8538","reticulosarcoma","icd9cm","200.7"
> "8538","reticulosarcoma","mesh","D008228"
> "8538","reticulosarcoma","umls","C0024302"
> "8538","reticulosarcoma","mondo","0009975"
> "8029","sporadic breast cancer","umls","C1336076"
> "8029","sporadic breast cancer","mondo","0004438"
> "8022","liver fibrosarcoma","umls","C1333966"
> "8022","liver fibrosarcoma","mondo","0004435"
> "15","reproductive system disease","umls","C1335037"
> "15","reproductive system disease","mondo","0005039"
> "8020","glomangiomyoma","umls","C0334422"
> "8020","glomangiomyoma","mondo","0024323"
> "8533","hypopharynx cancer","icd10cm","C13"
> "8533","hypopharynx cancer","icd10cm","C13.2"
> "8533","hypopharynx cancer","icd10cm","C13.9"
> "8533","hypopharynx cancer","icd9cm","148"
> "8533","hypopharynx cancer","icd9cm","148.3"
> "8533","hypopharynx cancer","icd9cm","148.9"
> "8533","hypopharynx cancer","mesh","D007012"
> "8533","hypopharynx cancer","umls","C0153398"
> "8533","hypopharynx cancer","umls","C0496770"
> "8533","hypopharynx cancer","mondo","0005806"
> "8534","gastroesophageal reflux disease","icd10cm","K21"
> "8534","gastroesophageal reflux disease","icd10cm","K21.9"
> "8534","gastroesophageal reflux disease","icd9cm","530.81"
> "8534","gastroesophageal reflux disease","mesh","D005764"
> "8534","gastroesophageal reflux disease","umls","C0017168"
> "8534","gastroesophageal reflux disease","mondo","0007186"
> "8536","herpes zoster","icd10cm","B02"
> "8536","herpes zoster","icd10cm","B02.9"
> "8536","herpes zoster","icd9cm","053"
> "8536","herpes zoster","mesh","D006562"
> "8536","herpes zoster","umls","C0019360"
> "8536","herpes zoster","mondo","0005609"
> "6407","ovarian surface papilloma","umls","C1335183"
> "6407","ovarian surface papilloma","mondo","0003873"
> "7441","chronic metabolic polyneuropathy","umls","C1333042"
> "7441","chronic metabolic polyneuropathy","mondo","0004224"
> "7442","monoclonal gammopathy of uncertain significance","mondo","0004225"
> "17","musculoskeletal system disease","mesh","D009140"
> "17","musculoskeletal system disease","umls","C0026857"
> "17","musculoskeletal system disease","mondo","0002081"
> "12474","capillariasis","icd10cm","B81.1"
> "12474","capillariasis","icd9cm","127.5"
> "12474","capillariasis","mesh","D017189"
> "12474","capillariasis","umls","C0006897"
> "12474","capillariasis","mondo","0001532"
> "0060799","syndromic X-linked intellectual disability Lubs type","mesh","C537723"
> "0060799","syndromic X-linked intellectual disability Lubs type","umls","C1846058"
> "0060799","syndromic X-linked intellectual disability Lubs type","mondo","0010283"
> "0060798","hypomyelinating leukodystrophy 6","icd10cm","E75.2"
> "0060798","hypomyelinating leukodystrophy 6","mondo","0012905"
> "0060063","sideroblastic anemia 1","mondo","0010419"
> "0060062","familial juvenile hyperuricemic nephropathy","mondo","0000608"
> "0060061","cutaneous T cell lymphoma","mesh","D016410"
> "0060061","cutaneous T cell lymphoma","mondo","0000607"
> "0060060","non-Hodgkin lymphoma","mesh","D008228"
> "0060060","non-Hodgkin lymphoma","mondo","0018908"
> "0060067","Pearson syndrome","mondo","0010797"
> "0060794","hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism","icd10cm","G11.1"
> "0060794","hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism","mondo","0011897"
> "0060797","hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism","icd10cm","G11.1"
> "0060797","hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism","mondo","0013722"
> "0060796","hypomyelinating leukodystrophy 12","mondo","0014732"
> "14755","argininosuccinic aciduria","mesh","D056807"
> "14755","argininosuccinic aciduria","umls","C0268547"
> "14755","argininosuccinic aciduria","mondo","0008815"
> "4283","anal margin basal cell carcinoma","icd10cm","C44.510"
> "4283","anal margin basal cell carcinoma","umls","C1332269"
> "4283","anal margin basal cell carcinoma","mondo","0002940"
> "4280","nodular basal cell carcinoma","umls","C1304300"
> "4280","nodular basal cell carcinoma","mondo","0002937"
> "4287","external ear basal cell carcinoma","umls","C1333491"
> "4287","external ear basal cell carcinoma","mondo","0002943"
> "4284","anal margin carcinoma","umls","C0349534"
> "4284","anal margin carcinoma","mondo","0002941"
> "13994","cleidocranial dysplasia","icd10cm","Q74.0"
> "13994","cleidocranial dysplasia","mesh","D002973"
> "13994","cleidocranial dysplasia","umls","C0008928"
> "13994","cleidocranial dysplasia","mondo","0007340"
> "4288","external ear carcinoma","umls","C1333492"
> "4288","external ear carcinoma","mondo","0002944"
> "0080223","epidermolytic palmoplantar keratoderma","mondo","0007758"
> "0080222","pseudohypoparathyroidism type IB","mesh","C548075"
> "0080222","pseudohypoparathyroidism type IB","mondo","0011301"
> "0080221","major affective disorder 2","mondo","0010648"
> "0080220","major affective disorder 1","mondo","0007440"
> "0080227","autosomal dominant mental retardation 55","mondo","0030921"
> "0080226","autosomal dominant mental retardation 56","mondo","0030922"
> "0080225","amyotrophic lateral sclerosis type 23","mondo","0027694"
> "0080224","autosomal dominant dystrophic epidermolysis bullosa","mondo","0007549"
> "0080228","autosomal dominant mental retardation 53","mondo","0030919"
> "2764","ethmoid sinus adenoid cystic carcinoma","umls","C1333473"
> "2764","ethmoid sinus adenoid cystic carcinoma","mondo","0006201"
> "381","arthropathy","icd10cm","M00-M02"
> "381","arthropathy","icd10cm","M12.9"
> "381","arthropathy","icd10cm","M19.90"
> "381","arthropathy","icd10cm","M25.9"
> "381","arthropathy","icd9cm","711"
> "381","arthropathy","icd9cm","716.9"
> "381","arthropathy","icd9cm","716.90"
> "381","arthropathy","icd9cm","719.9"
> "381","arthropathy","icd9cm","719.90"
> "381","arthropathy","mesh","D007592"
> "381","arthropathy","umls","C0022408"
> "381","arthropathy","umls","C0157749"
> "381","arthropathy","mondo","0006816"
> "384","Wolff-Parkinson-White syndrome","icd10cm","I45.6"
> "384","Wolff-Parkinson-White syndrome","icd9cm","426.7"
> "384","Wolff-Parkinson-White syndrome","mesh","D014927"
> "384","Wolff-Parkinson-White syndrome","umls","C0043202"
> "384","Wolff-Parkinson-White syndrome","umls","C0392470"
> "384","Wolff-Parkinson-White syndrome","mondo","0008685"
> "4751","striatonigral degeneration","icd10cm","G23.2"
> "4751","striatonigral degeneration","mesh","D020955"
> "4751","striatonigral degeneration","umls","C0270733"
> "4751","striatonigral degeneration","mondo","0003122"
> "4752","multiple system atrophy","mesh","D012791"
> "4752","multiple system atrophy","mesh","D019578"
> "4752","multiple system atrophy","umls","C0037019"
> "4752","multiple system atrophy","umls","C0393571"
> "4752","multiple system atrophy","mondo","0007803"
> "13662","ulcer of anus and rectum","icd10cm","K62.6"
> "13662","ulcer of anus and rectum","icd9cm","569.41"
> "13662","ulcer of anus and rectum","umls","C0400832"
> "13662","ulcer of anus and rectum","mondo","0001772"
> "13664","post-vaccinal encephalitis","icd10cm","G04.02"
> "13664","post-vaccinal encephalitis","mesh","D004673"
> "13664","post-vaccinal encephalitis","umls","C0751101"
> "13664","post-vaccinal encephalitis","mondo","0001773"
> "4756","testicular Leydig cell tumor","umls","C0863027"
> "4756","testicular Leydig cell tumor","mondo","0003124"
> "4757","testicular sex cord-stromal neoplasm","umls","C1515289"
> "4757","testicular sex cord-stromal neoplasm","mondo","0003125"
> "1076","chronic pyelonephritis","icd10cm","N11"
> "1076","chronic pyelonephritis","icd10cm","N11.9"
> "1076","chronic pyelonephritis","icd9cm","590.0"
> "1076","chronic pyelonephritis","umls","C0085697"
> "1076","chronic pyelonephritis","mondo","0001110"
> "5870","eosinophilic pneumonia","icd10cm","J82"
> "5870","eosinophilic pneumonia","mesh","D011657"
> "5870","eosinophilic pneumonia","umls","C1527407"
> "5870","eosinophilic pneumonia","mondo","0005749"
> "11299","vertebral artery occlusion","icd10cm","I65.0"
> "11299","vertebral artery occlusion","icd9cm","433.2"
> "11299","vertebral artery occlusion","umls","C0155724"
> "11299","vertebral artery occlusion","mondo","0001258"
> "5876","apocrine sweat gland neoplasm","umls","C1332318"
> "5876","apocrine sweat gland neoplasm","mondo","0003686"
> "5877","endocardium cancer","umls","C0346612"
> "5877","endocardium cancer","umls","C1290401"
> "5877","endocardium cancer","mondo","0003687"
> "5874","retroperitoneal germ cell neoplasm","umls","C1335776"
> "5874","retroperitoneal germ cell neoplasm","mondo","0003685"
> "5875","retroperitoneal cancer","icd10cm","C48"
> "5875","retroperitoneal cancer","icd10cm","C48.0"
> "5875","retroperitoneal cancer","icd9cm","158"
> "5875","retroperitoneal cancer","icd9cm","158.0"
> "5875","retroperitoneal cancer","mesh","D012186"
> "5875","retroperitoneal cancer","umls","C0035358"
> "5875","retroperitoneal cancer","umls","C0153464"
> "5875","retroperitoneal cancer","umls","C0153465"
> "5875","retroperitoneal cancer","mondo","0005941"
> "11294","arteriovenous malformation","icd10cm","I77.0"
> "11294","arteriovenous malformation","umls","C0334533"
> "11294","arteriovenous malformation","mondo","0001256"
> "11295","retinal microaneurysm","icd9cm","362.14"
> "11295","retinal microaneurysm","mesh","D000071071"
> "11295","retinal microaneurysm","umls","C0154834"
> "11295","retinal microaneurysm","mondo","0001257"
> "3751","plantar verrucous skin carcinoma","umls","C1335424"
> "3751","plantar verrucous skin carcinoma","mondo","0002765"
> "3750","urethra squamous cell carcinoma","umls","C1336890"
> "3750","urethra squamous cell carcinoma","mondo","0002764"
> "3753","Hermansky-Pudlak syndrome","icd10cm","E70.331"
> "3753","Hermansky-Pudlak syndrome","mesh","D022861"
> "3753","Hermansky-Pudlak syndrome","umls","C0079504"
> "3753","Hermansky-Pudlak syndrome","mondo","0019312"
> "3752","larynx verrucous carcinoma","umls","C0280328"
> "3752","larynx verrucous carcinoma","mondo","0002766"
> "3755","antithrombin III deficiency","icd10cm","D68.59"
> "3755","antithrombin III deficiency","mesh","D020152"
> "3755","antithrombin III deficiency","umls","C0272375"
> "3755","antithrombin III deficiency","mondo","0013144"
> "3756","protein C deficiency","icd10cm","D68.59"
> "3756","protein C deficiency","mesh","D020151"
> "3756","protein C deficiency","umls","C0398625"
> "3756","protein C deficiency","mondo","0019145"
> "4633","nasal cavity inverting papilloma","umls","C0280336"
> "4633","nasal cavity inverting papilloma","mondo","0003065"
> "13523","loiasis","icd10cm","B74.3"
> "13523","loiasis","icd9cm","125.2"
> "13523","loiasis","mesh","D008118"
> "13523","loiasis","umls","C0023968"
> "13523","loiasis","mondo","0016566"
> "13520","neonatal infective mastitis","icd10cm","P39.0"
> "13520","neonatal infective mastitis","icd9cm","771.5"
> "13520","neonatal infective mastitis","umls","C0158948"
> "13520","neonatal infective mastitis","mondo","0001736"
> "4630","inverted transitional papilloma","umls","C0334269"
> "4630","inverted transitional papilloma","mondo","0003064"
> "4637","cervical adenitis","umls","C0149642"
> "4637","cervical adenitis","mondo","0003067"
> "4636","submandibular adenitis","umls","C0235591"
> "4636","submandibular adenitis","mondo","0003066"
> "4639","suppurative lymphadenitis","umls","C0392051"
> "4639","suppurative lymphadenitis","mondo","0003069"
> "4638","postauricular lymphadenitis","umls","C0919638"
> "4638","postauricular lymphadenitis","mondo","0003068"
> "11746","parametrium malignant neoplasm","icd10cm","C57.3"
> "11746","parametrium malignant neoplasm","icd9cm","183.4"
> "11746","parametrium malignant neoplasm","umls","C0153581"
> "11746","parametrium malignant neoplasm","mondo","0001350"
> "11747","uterine adnexa cancer","icd10cm","C57.4"
> "11747","uterine adnexa cancer","icd9cm","183"
> "11747","uterine adnexa cancer","icd9cm","183.9"
> "11747","uterine adnexa cancer","umls","C0153577"
> "11747","uterine adnexa cancer","umls","C0153584"
> "11747","uterine adnexa cancer","mondo","0001351"
> "11748","round ligament malignant neoplasm","icd10cm","C57.2"
> "11748","round ligament malignant neoplasm","icd9cm","183.5"
> "11748","round ligament malignant neoplasm","umls","C0346867"
> "11748","round ligament malignant neoplasm","mondo","0001352"
> "7868","maxillary sinus inverted papilloma","umls","C1334645"
> "7868","maxillary sinus inverted papilloma","mondo","0004384"
> "0111272","occipital horn syndrome","mesh","C537860"
> "0111272","occipital horn syndrome","umls","C0268353"
> "0110289","autosomal recessive limb-girdle muscular dystrophy type 2Y","icd10cm","G71.0"
> "0110289","autosomal recessive limb-girdle muscular dystrophy type 2Y","mondo","0014900"
> "2047","hepatitis D","mesh","D003699"
> "2047","hepatitis D","umls","C0011226"
> "2047","hepatitis D","mondo","0005789"
> "0080217","lysosomal and lipase deficiency","mondo","0010204"
> "169","neuroendocrine tumor","icd10cm","D3A.8"
> "169","neuroendocrine tumor","icd9cm","209"
> "169","neuroendocrine tumor","icd9cm","209-209.99"
> "169","neuroendocrine tumor","mesh","D018358"
> "169","neuroendocrine tumor","umls","C0206754"
> "169","neuroendocrine tumor","mondo","0019496"
> "166","melanotic neuroectodermal tumor","mesh","D017600"
> "166","melanotic neuroectodermal tumor","umls","C0206094"
> "166","melanotic neuroectodermal tumor","mondo","0002072"
> "161","keratosis","mesh","D007642"
> "161","keratosis","umls","C0022593"
> "161","keratosis","mondo","0006566"
> "162","cancer","icd10cm","C80"
> "162","cancer","icd10cm","C80.1"
> "162","cancer","icd9cm","199"
> "162","cancer","mesh","D009369"
> "162","cancer","umls","C0006826"
> "162","cancer","mondo","0004992"
> "13651","eversion of lacrimal punctum","icd10cm","H04.52"
> "13651","eversion of lacrimal punctum","icd9cm","375.51"
> "13651","eversion of lacrimal punctum","umls","C0155243"
> "13651","eversion of lacrimal punctum","mondo","0001766"
> "6195","conjunctivitis","icd10cm","H10"
> "6195","conjunctivitis","icd10cm","H10.9"
> "6195","conjunctivitis","icd9cm","372.30"
> "6195","conjunctivitis","mesh","D003231"
> "6195","conjunctivitis","umls","C0009763"
> "6195","conjunctivitis","mondo","0003799"
> "6196","reactive arthritis","icd10cm","M02.1"
> "6196","reactive arthritis","icd10cm","M02.10"
> "6196","reactive arthritis","icd10cm","M02.3"
> "6196","reactive arthritis","icd10cm","M02.30"
> "6196","reactive arthritis","icd9cm","099.3"
> "6196","reactive arthritis","icd9cm","711.3"
> "6196","reactive arthritis","icd9cm","711.30"
> "6196","reactive arthritis","mesh","D016918"
> "6196","reactive arthritis","umls","C0035012"
> "6196","reactive arthritis","umls","C0152085"
> "6196","reactive arthritis","mondo","0017376"
> "6197","conventional malignant hemangiopericytoma","umls","C1333158"
> "6197","conventional malignant hemangiopericytoma","mondo","0003800"
> "6190","rectum Kaposi's sarcoma","umls","C1335681"
> "6190","rectum Kaposi's sarcoma","mondo","0003796"
> "6192","inflammatory MFH","umls","C1334180"
> "6192","inflammatory MFH","mondo","0006480"
> "6193","epithelioid sarcoma","umls","C0205944"
> "6193","epithelioid sarcoma","mondo","0017387"
> "6741","bilateral breast cancer","umls","C0281267"
> "6741","bilateral breast cancer","mondo","0003982"
> "0111274","CODAS syndrome","mesh","C536434"
> "0111274","CODAS syndrome","umls","C1838180"
> "6198","corneal intraepithelial neoplasm","umls","C1333159"
> "6198","corneal intraepithelial neoplasm","mondo","0003801"
> "6199","cornea cancer","icd10cm","C69.1"
> "6199","cornea cancer","icd9cm","190.4"
> "6199","cornea cancer","umls","C0153629"
> "6199","cornea cancer","umls","C0339304"
> "6199","cornea cancer","mondo","0003802"
> "6740","cervix small cell carcinoma","umls","C0279674"
> "6740","cervix small cell carcinoma","mondo","0006142"
> "2734","keratosis follicularis","icd10cm","E50.8"
> "2734","keratosis follicularis","mesh","D007644"
> "2734","keratosis follicularis","umls","C0022595"
> "2734","keratosis follicularis","mondo","0007417"
> "2736","Hajdu-Cheney syndrome","mesh","D030981"
> "2736","Hajdu-Cheney syndrome","mesh","D031845"
> "2736","Hajdu-Cheney syndrome","umls","C0917715"
> "2736","Hajdu-Cheney syndrome","umls","C0917990"
> "2736","Hajdu-Cheney syndrome","mondo","0007057"
> "2730","epidermolysis bullosa","icd10cm","Q81"
> "2730","epidermolysis bullosa","icd10cm","Q81.9"
> "2730","epidermolysis bullosa","mesh","D004820"
> "2730","epidermolysis bullosa","umls","C0014527"
> "2730","epidermolysis bullosa","mondo","0006541"
> "2731","vesiculobullous skin disease","mesh","D012872"
> "2731","vesiculobullous skin disease","umls","C0037275"
> "2731","vesiculobullous skin disease","mondo","0006617"
> "2732","Rothmund-Thomson syndrome","icd10cm","Q82.8"
> "2732","Rothmund-Thomson syndrome","mesh","D011038"
> "2732","Rothmund-Thomson syndrome","umls","C0032339"
> "2732","Rothmund-Thomson syndrome","mondo","0010002"
> "2733","skin atrophy","icd10cm","L90"
> "2733","skin atrophy","icd10cm","L90.9"
> "2733","skin atrophy","umls","C0151514"
> "2733","skin atrophy","mondo","0006610"
> "2738","pseudoxanthoma elasticum","mesh","D011561"
> "2738","pseudoxanthoma elasticum","umls","C0033847"
> "2738","pseudoxanthoma elasticum","mondo","0009925"
> "2739","Gilbert syndrome","icd10cm","E80.4"
> "2739","Gilbert syndrome","mesh","D005878"
> "2739","Gilbert syndrome","umls","C0017551"
> "2739","Gilbert syndrome","mondo","0007745"
> "13658","infective urethral stricture","icd9cm","598.01"
> "13658","infective urethral stricture","umls","C0156282"
> "13658","infective urethral stricture","mondo","0001771"
> "9182","pemphigus","icd10cm","L10"
> "9182","pemphigus","icd10cm","L10.9"
> "9182","pemphigus","icd9cm","694.4"
> "9182","pemphigus","mesh","D010392"
> "9182","pemphigus","umls","C0030807"
> "9182","pemphigus","mondo","0006594"
> "10368","epididymis adenocarcinoma","umls","C1510784"
> "10368","epididymis adenocarcinoma","mondo","0001017"
> "9181","amebiasis","icd10cm","A06"
> "9181","amebiasis","icd10cm","A06.9"
> "9181","amebiasis","icd9cm","006"
> "9181","amebiasis","icd9cm","006.9"
> "9181","amebiasis","mesh","D000562"
> "9181","amebiasis","umls","C0002438"
> "9181","amebiasis","mondo","0005644"
> "678","progressive supranuclear palsy","icd10cm","G23.1"
> "678","progressive supranuclear palsy","mesh","D013494"
> "678","progressive supranuclear palsy","umls","C0038868"
> "678","progressive supranuclear palsy","mondo","0019037"
> "10366","epididymis cancer","icd10cm","C63.0"
> "10366","epididymis cancer","icd9cm","187.5"
> "10366","epididymis cancer","umls","C0153602"
> "10366","epididymis cancer","mondo","0001016"
> "10361","eosinophilic meningitis","icd9cm","322.1"
> "10361","eosinophilic meningitis","umls","C0154652"
> "10361","eosinophilic meningitis","mondo","0001015"
> "9188","vestibule of mouth cancer","icd10cm","C06.1"
> "9188","vestibule of mouth cancer","icd9cm","145.1"
> "9188","vestibule of mouth cancer","umls","C0153374"
> "9188","vestibule of mouth cancer","mondo","0004727"
> "679","basal ganglia disease","mesh","D001480"
> "679","basal ganglia disease","umls","C0004782"
> "679","basal ganglia disease","mondo","0003996"
> "0110140","Bardet-Biedl syndrome 18","icd10cm","Q87.89"
> "0110140","Bardet-Biedl syndrome 18","mondo","0014446"
> "0110141","Bardet-Biedl syndrome 19","icd10cm","Q87.89"
> "0110141","Bardet-Biedl syndrome 19","mondo","0014447"
> "0110142","Bartter disease type 1","icd10cm","E26.8"
> "0110142","Bartter disease type 1","mondo","0011127"
> "0110143","Bartter disease type 2","icd10cm","E26.8"
> "0110143","Bartter disease type 2","mondo","0009424"
> "0110144","Bartter disease type 3","icd10cm","E26.8"
> "0110144","Bartter disease type 3","mondo","0011822"
> "0110145","Bartter disease type 4a","icd10cm","E26.8"
> "0110145","Bartter disease type 4a","mondo","0011242"
> "0110146","Bartter disease type 4b","icd10cm","E26.8"
> "0110146","Bartter disease type 4b","mondo","0000909"
> "0110147","Bartter disease type 5","icd10cm","E26.8"
> "0110147","Bartter disease type 5","mondo","0010503"
> "0110148","Charcot-Marie-Tooth disease type 1A","icd10cm","G60.0"
> "0110148","Charcot-Marie-Tooth disease type 1A","mondo","0007309"
> "7202","intermediate malignant teratoma","umls","C0334522"
> "7202","intermediate malignant teratoma","mondo","0004140"
> "7207","lung combined large cell neuroendocrine carcinoma","umls","C1333122"
> "7207","lung combined large cell neuroendocrine carcinoma","mondo","0004142"
> "7206","melanomatosis","umls","C1334691"
> "7206","melanomatosis","mondo","0004141"
> "12211","filarial elephantiasis","icd10cm","B74.0"
> "12211","filarial elephantiasis","mesh","D004605"
> "12211","filarial elephantiasis","umls","C0013884"
> "12211","filarial elephantiasis","mondo","0005761"
> "12253","testicular lymphoma","umls","C0349644"
> "12253","testicular lymphoma","mondo","0001472"
> "12217","Lewy body dementia","icd10cm","G31.83"
> "12217","Lewy body dementia","icd9cm","331.82"
> "12217","Lewy body dementia","mesh","D020961"
> "12217","Lewy body dementia","umls","C0752347"
> "12217","Lewy body dementia","mondo","0007488"
> "6227","articular cartilage disease","icd9cm","718.0"
> "6227","articular cartilage disease","icd9cm","718.00"
> "6227","articular cartilage disease","umls","C0158073"
> "6227","articular cartilage disease","mondo","0003816"
> "12215","oligohydramnios","icd10cm","O41.0"
> "12215","oligohydramnios","icd10cm","O41.00"
> "12215","oligohydramnios","icd9cm","658.0"
> "12215","oligohydramnios","mesh","D016104"
> "12215","oligohydramnios","umls","C0079924"
> "12215","oligohydramnios","mondo","0005881"
> "6225","Cronkhite-Canada syndrome","umls","C1333764"
> "6225","Cronkhite-Canada syndrome","mondo","0008283"
> "6228","peritoneal serous papillary adenocarcinoma","umls","C1368918"
> "6228","peritoneal serous papillary adenocarcinoma","mondo","0003817"
> "6229","childhood mature teratoma of the ovary","umls","C1332991"
> "6229","childhood mature teratoma of the ovary","mondo","0003818"
> "11613","hyperandrogenism","mesh","D017588"
> "11613","hyperandrogenism","umls","C0206081"
> "11613","hyperandrogenism","mondo","0001324"
> "13976","peptic esophagitis","icd9cm","530.11"
> "13976","peptic esophagitis","mesh","D004942"
> "13976","peptic esophagitis","umls","C0014869"
> "13976","peptic esophagitis","mondo","0006896"
> "9766","xanthogranulomatous cholecystitis","mesh","C536762"
> "9766","xanthogranulomatous cholecystitis","umls","C1337035"
> "9766","xanthogranulomatous cholecystitis","mondo","0004875"
> "9767","myocardial stunning","mesh","D017682"
> "9767","myocardial stunning","umls","C0206146"
> "9767","myocardial stunning","mondo","0004876"
> "9765","emphysematous cholecystitis","mesh","D041882"
> "9765","emphysematous cholecystitis","umls","C0521610"
> "9765","emphysematous cholecystitis","mondo","0005742"
> "9768","heart aneurysm","icd10cm","I25.3"
> "9768","heart aneurysm","mesh","D006322"
> "9768","heart aneurysm","umls","C0018789"
> "9768","heart aneurysm","mondo","0006779"
> "10507","Dressler's syndrome","icd10cm","I24.1"
> "10507","Dressler's syndrome","icd9cm","411.0"
> "10507","Dressler's syndrome","umls","C0152107"
> "10507","Dressler's syndrome","mondo","0001049"
> "809","cocaine abuse","icd10cm","F14.1"
> "809","cocaine abuse","icd9cm","305.6"
> "809","cocaine abuse","icd9cm","305.60"
> "809","cocaine abuse","mesh","D019970"
> "809","cocaine abuse","umls","C0009171"
> "809","cocaine abuse","mondo","0004456"
> "8858","tonsil cancer","icd10cm","C09"
> "8858","tonsil cancer","icd10cm","C09.9"
> "8858","tonsil cancer","icd9cm","146.0"
> "8858","tonsil cancer","mesh","D014067"
> "8858","tonsil cancer","umls","C0751560"
> "8858","tonsil cancer","mondo","0006998"
> "801","hemarthrosis","icd10cm","M25.0"
> "801","hemarthrosis","icd9cm","719.1"
> "801","hemarthrosis","icd9cm","719.10"
> "801","hemarthrosis","mesh","D006395"
> "801","hemarthrosis","umls","C0018924"
> "801","hemarthrosis","mondo","0004431"
> "8850","salivary gland cancer","icd10cm","C08"
> "8850","salivary gland cancer","icd9cm","142.8"
> "8850","salivary gland cancer","umls","C0153362"
> "8850","salivary gland cancer","mondo","0004669"
> "807","carotid artery occlusion","icd9cm","433.10"
> "807","carotid artery occlusion","umls","C0375275"
> "807","carotid artery occlusion","mondo","0004450"
> "11246","DIC in newborn","icd10cm","P60"
> "11246","DIC in newborn","icd9cm","776.2"
> "11246","DIC in newborn","umls","C0158992"
> "11246","DIC in newborn","mondo","0001242"
> "13450","coccidioidomycosis","icd10cm","B38"
> "13450","coccidioidomycosis","icd10cm","B38.9"
> "13450","coccidioidomycosis","icd9cm","114"
> "13450","coccidioidomycosis","icd9cm","114.9"
> "13450","coccidioidomycosis","mesh","D003047"
> "13450","coccidioidomycosis","umls","C0009186"
> "13450","coccidioidomycosis","mondo","0005706"
> "5274","malignant dermis tumor","umls","C0346811"
> "5274","malignant dermis tumor","mondo","0003363"
> "5275","gallbladder leiomyosarcoma","umls","C1333746"
> "5275","gallbladder leiomyosarcoma","mondo","0003364"
> "5276","esophagus leiomyosarcoma","umls","C1333454"
> "5276","esophagus leiomyosarcoma","mondo","0003365"
> "1776","labyrinthine unilateral reactive loss","icd9cm","386.55"
> "1776","labyrinthine unilateral reactive loss","umls","C0155519"
> "1776","labyrinthine unilateral reactive loss","mondo","0002106"
> "5271","small intestine leiomyosarcoma","umls","C0920305"
> "5271","small intestine leiomyosarcoma","mondo","0003360"
> "5272","small intestinal sarcoma","umls","C1336007"
> "5272","small intestinal sarcoma","mondo","0003361"
> "5273","cutaneous leiomyosarcoma","umls","C0346067"
> "5273","cutaneous leiomyosarcoma","mondo","0003362"
> "11949","Creutzfeldt-Jakob disease","icd10cm","A81.0"
> "11949","Creutzfeldt-Jakob disease","icd10cm","A81.00"
> "11949","Creutzfeldt-Jakob disease","icd9cm","046.1"
> "11949","Creutzfeldt-Jakob disease","mesh","D007562"
> "11949","Creutzfeldt-Jakob disease","umls","C0022336"
> "11949","Creutzfeldt-Jakob disease","mondo","0005357"
> "0040098","pemphigus gestationis","icd10cm","O26.4"
> "0040098","pemphigus gestationis","mesh","D006559"
> "0040098","pemphigus gestationis","mondo","0006558"
> "0040099","livedoid vasculitis","icd10cm","L95.0"
> "0040099","livedoid vasculitis","icd9cm","709.1"
> "0040099","livedoid vasculitis","mondo","0025514"
> "0040091","autoimmune pancreatitis","umls","C2609129"
> "0040091","autoimmune pancreatitis","mondo","0015175"
> "0040092","juvenile ankylosing spondylitis","icd10cm","M08.1"
> "0040092","juvenile ankylosing spondylitis","umls","C0409675"
> "0040092","juvenile ankylosing spondylitis","mondo","0020655"
> "0040093","drug-induced lupus erythematosus","icd10cm","M32.0"
> "0040093","drug-induced lupus erythematosus","umls","C0263591"
> "0040093","drug-induced lupus erythematosus","mondo","0016474"
> "0040097","autoimmune vasculitis","umls","C1328843"
> "0040097","autoimmune vasculitis","mondo","0030703"
> "0111540","prolidase deficiency","mesh","D056732"
> "0111540","prolidase deficiency","umls","C0268532"
> "10319","mixed mineral dust pneumoconiosis","umls","C0340184"
> "10319","mixed mineral dust pneumoconiosis","mondo","0001000"
> "3038","submucosal invasive colon adenocarcinoma","umls","C1515024"
> "3038","submucosal invasive colon adenocarcinoma","mondo","0002496"
> "3039","cecum adenocarcinoma","umls","C1332866"
> "3039","cecum adenocarcinoma","mondo","0006028"
> "1557","hypersensitivity reaction type III disease","mesh","D007105"
> "1557","hypersensitivity reaction type III disease","umls","C0020951"
> "1557","hypersensitivity reaction type III disease","mondo","0007004"
> "1556","arthus reaction","icd10cm","T78.41"
> "1556","arthus reaction","icd9cm","995.21"
> "1556","arthus reaction","mesh","D001183"
> "1556","arthus reaction","umls","C0003907"
> "1556","arthus reaction","mondo","0006660"
> "11102","bartonellosis","icd10cm","A44"
> "11102","bartonellosis","icd10cm","A44.9"
> "11102","bartonellosis","icd9cm","088.0"
> "11102","bartonellosis","mesh","D001474"
> "11102","bartonellosis","umls","C0004771"
> "11102","bartonellosis","mondo","0005664"
> "11103","rickettsialpox","icd10cm","A79.1"
> "11103","rickettsialpox","icd9cm","083.2"
> "11103","rickettsialpox","mesh","D000073605"
> "11103","rickettsialpox","umls","C0035597"
> "11103","rickettsialpox","mondo","0019360"
> "11100","Q fever","icd10cm","A78"
> "11100","Q fever","icd9cm","083.0"
> "11100","Q fever","mesh","D011778"
> "11100","Q fever","umls","C0034362"
> "11100","Q fever","mondo","0019186"
> "11101","trench fever","icd10cm","A79.0"
> "11101","trench fever","icd9cm","083.1"
> "11101","trench fever","mesh","D014205"
> "11101","trench fever","umls","C0040830"
> "11101","trench fever","mondo","0005991"
> "3030","mucinous adenocarcinoma","mesh","D002288"
> "3030","mucinous adenocarcinoma","umls","C0007130"
> "3030","mucinous adenocarcinoma","umls","C0334368"
> "3030","mucinous adenocarcinoma","mondo","0004957"
> "11104","spotted fever","icd10cm","A77"
> "11104","spotted fever","icd10cm","A77.9"
> "11104","spotted fever","icd9cm","082.0"
> "11104","spotted fever","mesh","D000073605"
> "11104","spotted fever","umls","C0038041"
> "11104","spotted fever","mondo","0001195"
> "11105","fundus albipunctatus","icd10cm","H35.52"
> "11105","fundus albipunctatus","icd9cm","362.74"
> "11105","fundus albipunctatus","mesh","C562733"
> "11105","fundus albipunctatus","umls","C0311338"
> "11105","fundus albipunctatus","mondo","0007639"
> "8702","cheek mucosa cancer","icd10cm","C06.0"
> "8702","cheek mucosa cancer","icd9cm","145.0"
> "8702","cheek mucosa cancer","umls","C0153373"
> "8702","cheek mucosa cancer","mondo","0004645"
> "8704","genital herpes","icd9cm","054.1"
> "8704","genital herpes","icd9cm","054.10"
> "8704","genital herpes","mesh","D006558"
> "8704","genital herpes","umls","C0019342"
> "8704","genital herpes","mondo","0005770"
> "0060474","familial erythrocytosis 2","icd10cm","D75.1"
> "0060474","familial erythrocytosis 2","mondo","0009892"
> "0060475","childhood onset epileptic encephalopathy","mondo","0014150"
> "0060476","Perlman syndrome","icd10cm","Q87.3"
> "0060476","Perlman syndrome","mesh","C536399"
> "0060476","Perlman syndrome","mondo","0009965"
> "0060470","salt and pepper syndrome","mondo","0018275"
> "0060471","fetal valproate syndrome","mesh","C536525"
> "0060471","fetal valproate syndrome","umls","C0236026"
> "0060471","fetal valproate syndrome","mondo","0012275"
> "0060472","Kindler syndrome","mesh","C536321"
> "0060472","Kindler syndrome","mondo","0008260"
> "0060473","Kabuki syndrome","mesh","C537705"
> "0060473","Kabuki syndrome","umls","C0796004"
> "0060473","Kabuki syndrome","mondo","0016512"
> "0060478","Zika fever","icd10cm","A92.8"
> "0060478","Zika fever","mesh","D000071243"
> "0060478","Zika fever","mondo","0018661"
> "0060479","Shwachman-Diamond syndrome","icd10cm","D61.0"
> "0060479","Shwachman-Diamond syndrome","mesh","C537330"
> "0060479","Shwachman-Diamond syndrome","mondo","0009833"
> "5605","breast medullary carcinoma","umls","C0860580"
> "5605","breast medullary carcinoma","mondo","0005063"
> "5604","adult acute lymphocytic leukemia","umls","C0751606"
> "5604","adult acute lymphocytic leukemia","mondo","0003541"
> "5600","precursor lymphoblastic lymphoma/leukemia","umls","C1335469"
> "5600","precursor lymphoblastic lymphoma/leukemia","mondo","0003538"
> "5603","acute T cell leukemia","icd10cm","C91.5"
> "5603","acute T cell leukemia","icd10cm","C91.50"
> "5603","acute T cell leukemia","mesh","D015459"
> "5603","acute T cell leukemia","umls","C0023493"
> "5603","acute T cell leukemia","mondo","0003540"
> "5602","T-cell adult acute lymphocytic leukemia","umls","C0279592"
> "5602","T-cell adult acute lymphocytic leukemia","mondo","0003539"
> "205","hyperostosis","icd10cm","M89.3"
> "205","hyperostosis","icd10cm","M89.30"
> "205","hyperostosis","mesh","D015576"
> "205","hyperostosis","umls","C0020492"
> "205","hyperostosis","mondo","0002185"
> "5608","dental pulp calcification","icd10cm","K04.2"
> "5608","dental pulp calcification","mesh","D003784"
> "5608","dental pulp calcification","umls","C0011401"
> "5608","dental pulp calcification","mondo","0003542"
> "204","enthesopathy","icd10cm","M77.9"
> "204","enthesopathy","icd9cm","726.9"
> "204","enthesopathy","icd9cm","726.90"
> "204","enthesopathy","mesh","D000070676"
> "204","enthesopathy","umls","C0242490"
> "204","enthesopathy","mondo","0002183"
> "206","hereditary multiple exostoses","icd10cm","Q78.6"
> "206","hereditary multiple exostoses","mesh","D005097"
> "206","hereditary multiple exostoses","umls","C0015306"
> "206","hereditary multiple exostoses","mondo","0005508"
> "0110499","autosomal recessive nonsyndromic deafness 40","icd10cm","H90.3"
> "0110499","autosomal recessive nonsyndromic deafness 40","mondo","0012002"
> "11968","postmenopausal atrophic vaginitis","icd10cm","N95.2"
> "11968","postmenopausal atrophic vaginitis","icd9cm","627.3"
> "11968","postmenopausal atrophic vaginitis","umls","C0156409"
> "11968","postmenopausal atrophic vaginitis","mondo","0001410"
> "13317","hyperinsulinemic hypoglycemia","icd10cm","E16.9"
> "13317","hyperinsulinemic hypoglycemia","mesh","D046768"
> "13317","hyperinsulinemic hypoglycemia","umls","C0027773"
> "13317","hyperinsulinemic hypoglycemia","mondo","0005803"
> "6425","eyelid carcinoma","umls","C0920196"
> "6425","eyelid carcinoma","mondo","0003876"
> "6420","pulmonary valve stenosis","mesh","D011666"
> "6420","pulmonary valve stenosis","umls","C0034089"
> "6420","pulmonary valve stenosis","mondo","0006936"
> "12450","pancytopenia","icd10cm","D61.81"
> "12450","pancytopenia","icd9cm","284.1"
> "12450","pancytopenia","mesh","D010198"
> "12450","pancytopenia","umls","C0030312"
> "12450","pancytopenia","mondo","0001529"
> "6423","childhood central nervous system mature teratoma","umls","C1332955"
> "6423","childhood central nervous system mature teratoma","mondo","0003875"
> "6428","cervical adenoid basal carcinoma","umls","C1516403"
> "6428","cervical adenoid basal carcinoma","mondo","0006132"
> "0110962","brachydactyly-preaxial hallux varus syndrome","icd10cm","Q73.8"
> "0110962","brachydactyly-preaxial hallux varus syndrome","mondo","0007214"
> "0110963","Ballard syndrome","icd10cm","Q73.8"
> "0110963","Ballard syndrome","mondo","0007213"
> "0110960","Gaucher's disease perinatal lethal","icd10cm","E75.2"
> "0110960","Gaucher's disease perinatal lethal","mondo","0011945"
> "0110961","atypical Gaucher's disease due to saposin c deficiency","icd10cm","E75.2"
> "0110961","atypical Gaucher's disease due to saposin c deficiency","mondo","0012517"
> "0110966","brachydactyly type A3","mondo","0007217"
> "0110967","brachydactyly type A4","icd10cm","Q73.8"
> "0110967","brachydactyly type A4","mondo","0007218"
> "0110964","brachydactyly type A1","mondo","0007215"
> "0110965","brachydactyly type A2","mesh","C537089"
> "0110965","brachydactyly type A2","umls","C1832702"
> "0110965","brachydactyly type A2","mondo","0007216"
> "0110968","brachydactyly type A6","mesh","C537092"
> "0110968","brachydactyly type A6","umls","C1862130"
> "0110968","brachydactyly type A6","mondo","0007219"
> "0110969","brachydactyly type B1","mondo","0007220"
> "6762","sternum lymphoma","umls","C1336504"
> "6762","sternum lymphoma","mondo","0003988"
> "6760","lung lymphoma","umls","C0519063"
> "6760","lung lymphoma","mondo","0003987"
> "9977","hallucinogen dependence","icd10cm","F16.2"
> "9977","hallucinogen dependence","icd9cm","304.5"
> "9977","hallucinogen dependence","icd9cm","304.50"
> "9977","hallucinogen dependence","umls","C0018528"
> "9977","hallucinogen dependence","mondo","0004939"
> "9976","heroin dependence","mesh","D006556"
> "9976","heroin dependence","umls","C0019337"
> "9976","heroin dependence","mondo","0005367"
> "9975","cocaine dependence","icd10cm","F14.2"
> "9975","cocaine dependence","icd9cm","304.2"
> "9975","cocaine dependence","icd9cm","304.20"
> "9975","cocaine dependence","mesh","D019970"
> "9975","cocaine dependence","umls","C0600427"
> "9975","cocaine dependence","mondo","0005186"
> "9974","drug dependence","icd9cm","304.6"
> "9974","drug dependence","icd9cm","304.60"
> "9974","drug dependence","umls","C0029792"
> "9974","drug dependence","mondo","0005303"
> "9973","substance dependence","umls","C0439857"
> "9973","substance dependence","mondo","0004938"
> "9972","hypervitaminosis A","icd10cm","E67.0"
> "9972","hypervitaminosis A","icd9cm","278.2"
> "9972","hypervitaminosis A","mesh","D006986"
> "9972","hypervitaminosis A","umls","C0020579"
> "9972","hypervitaminosis A","mondo","0006798"
> "9971","hypervitaminosis D","icd10cm","E67.3"
> "9971","hypervitaminosis D","icd9cm","278.4"
> "9971","hypervitaminosis D","umls","C1442839"
> "9971","hypervitaminosis D","mondo","0004937"
> "9970","obesity","icd10cm","E66.9"
> "9970","obesity","icd9cm","278.00"
> "9970","obesity","mesh","D009765"
> "9970","obesity","umls","C0028754"
> "9970","obesity","mondo","0011122"
> "9978","acute female pelvic peritonitis","icd10cm","N73.3"
> "9978","acute female pelvic peritonitis","icd9cm","614.5"
> "9978","acute female pelvic peritonitis","umls","C0269032"
> "9978","acute female pelvic peritonitis","mondo","0004940"
> "0060816","corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome","icd10cm","Q87.8"
> "0060816","corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome","mondo","0010333"
> "0060817","syndromic X-linked intellectual disability 34","mondo","0010501"
> "0060814","Wilson-Turner syndrome","mondo","0010665"
> "0060815","Miles-Carpenter syndrome","mesh","C537472"
> "0060815","Miles-Carpenter syndrome","umls","C1839735"
> "0060815","Miles-Carpenter syndrome","mondo","0010666"
> "0060812","syndromic X-linked intellectual disability Siderius type","mesh","C537333"
> "0060812","syndromic X-linked intellectual disability Siderius type","umls","C1846055"
> "0060812","syndromic X-linked intellectual disability Siderius type","mondo","0010286"
> "0060813","syndromic X-linked intellectual disability Shrimpton type","icd10cm","Q87.8"
> "0060813","syndromic X-linked intellectual disability Shrimpton type","mondo","0010409"
> "0060810","syndromic X-linked intellectual disability type 10","icd10cm","G25.5"
> "0060810","syndromic X-linked intellectual disability type 10","mondo","0010272"
> "0060811","syndromic X-linked intellectual disability Turner type","icd10cm","Q87.8"
> "0060811","syndromic X-linked intellectual disability Turner type","mondo","0010407"
> "0060818","syndromic X-linked intellectual disability Abidi type","mesh","C535556"
> "0060818","syndromic X-linked intellectual disability Abidi type","umls","C1846056"
> "0060818","syndromic X-linked intellectual disability Abidi type","mondo","0010285"
> "0060819","syndromic X-linked intellectual disability Chudley-Schwartz type","mondo","0010462"
> "229","female reproductive system disease","icd9cm","629.9"
> "229","female reproductive system disease","mesh","D005831"
> "229","female reproductive system disease","umls","C0017411"
> "229","female reproductive system disease","mondo","0002263"
> "227","ankylosis","icd10cm","M24.6"
> "227","ankylosis","icd9cm","718.5"
> "227","ankylosis","icd9cm","718.50"
> "227","ankylosis","mesh","D000844"
> "227","ankylosis","umls","C0003090"
> "227","ankylosis","mondo","0002257"
> "225","syndrome","mesh","D013577"
> "225","syndrome","umls","C0039082"
> "225","syndrome","mondo","0002254"
> "224","transient cerebral ischemia","icd10cm","G45.9"
> "224","transient cerebral ischemia","mesh","D002546"
> "224","transient cerebral ischemia","umls","C0007787"
> "224","transient cerebral ischemia","mondo","0005264"
> "12028","Conn's syndrome","icd10cm","E26.0"
> "12028","Conn's syndrome","icd10cm","E26.01"
> "12028","Conn's syndrome","icd9cm","255.12"
> "12028","Conn's syndrome","mesh","D006929"
> "12028","Conn's syndrome","umls","C1384514"
> "12028","Conn's syndrome","mondo","0001422"
> "12029","sympathetic ophthalmia","icd10cm","H44.13"
> "12029","sympathetic ophthalmia","icd9cm","360.11"
> "12029","sympathetic ophthalmia","mesh","D009879"
> "12029","sympathetic ophthalmia","umls","C0029077"
> "12029","sympathetic ophthalmia","mondo","0019198"
> "221","acute perichondritis of pinna","icd9cm","380.01"
> "221","acute perichondritis of pinna","umls","C0155390"
> "221","acute perichondritis of pinna","mondo","0002240"
> "10223","dermatomyositis","icd10cm","M33"
> "10223","dermatomyositis","icd10cm","M33.9"
> "10223","dermatomyositis","icd10cm","M33.90"
> "10223","dermatomyositis","icd9cm","710.3"
> "10223","dermatomyositis","mesh","D003882"
> "10223","dermatomyositis","umls","C0011633"
> "10223","dermatomyositis","mondo","0016367"
> "0050428","nonepidermolytic palmoplantar keratoderma","mesh","D015776"
> "0050428","nonepidermolytic palmoplantar keratoderma","umls","C0022584"
> "0050428","nonepidermolytic palmoplantar keratoderma","umls","C3489771"
> "0050428","nonepidermolytic palmoplantar keratoderma","mondo","0006588"
> "0050429","Hailey-Hailey disease","icd10cm","Q82.8"
> "0050429","Hailey-Hailey disease","mesh","D016506"
> "0050429","Hailey-Hailey disease","umls","C0085106"
> "0050429","Hailey-Hailey disease","mondo","0008218"
> "0050424","familial adenomatous polyposis","mesh","D011125"
> "0050424","familial adenomatous polyposis","umls","C0032580"
> "0050424","familial adenomatous polyposis","mondo","0021055"
> "0050425","restless legs syndrome","icd10cm","G25.81"
> "0050425","restless legs syndrome","icd9cm","333.94"
> "0050425","restless legs syndrome","mesh","D012148"
> "0050425","restless legs syndrome","umls","C0035258"
> "0050425","restless legs syndrome","mondo","0005391"
> "0050426","Stevens-Johnson syndrome","icd10cm","L51.1"
> "0050426","Stevens-Johnson syndrome","icd10cm","L51.2"
> "0050426","Stevens-Johnson syndrome","icd9cm","695.13"
> "0050426","Stevens-Johnson syndrome","icd9cm","695.15"
> "0050426","Stevens-Johnson syndrome","mesh","D013262"
> "0050426","Stevens-Johnson syndrome","umls","C0014518"
> "0050426","Stevens-Johnson syndrome","umls","C0038325"
> "0050426","Stevens-Johnson syndrome","umls","C1274933"
> "0050426","Stevens-Johnson syndrome","umls","C3658301"
> "0050426","Stevens-Johnson syndrome","umls","C3658302"
> "0050426","Stevens-Johnson syndrome","mondo","0018229"
> "0050427","xeroderma pigmentosum","icd10cm","Q82.1"
> "0050427","xeroderma pigmentosum","mesh","D014983"
> "0050427","xeroderma pigmentosum","umls","C0043346"
> "0050427","xeroderma pigmentosum","mondo","0019600"
> "0111158","SADDAN","mesh","D000130"
> "0111158","SADDAN","umls","C2674173"
> "0111158","SADDAN","mondo","0014658"
> "10329","pneumoconiosis due to talc","icd10cm","J62.0"
> "10329","pneumoconiosis due to talc","umls","C0238377"
> "10329","pneumoconiosis due to talc","mondo","0001003"
> "2508","Takayasu's arteritis","icd10cm","M31.4"
> "2508","Takayasu's arteritis","icd9cm","446.7"
> "2508","Takayasu's arteritis","mesh","D001015"
> "2508","Takayasu's arteritis","mesh","D013625"
> "2508","Takayasu's arteritis","umls","C0003490"
> "2508","Takayasu's arteritis","umls","C0039263"
> "2508","Takayasu's arteritis","mondo","0017991"
> "0111154","postural orthostatic tachycardia syndrome","icd10cm","I95.1"
> "0111154","postural orthostatic tachycardia syndrome","mesh","D054972"
> "0111154","postural orthostatic tachycardia syndrome","mondo","0011479"
> "0111155","autosomal recessive spinocerebellar ataxia 21","mondo","0014744"
> "0111156","spermatogenic failure 9","mondo","0015746"
> "0111157","Castleman disease","icd10cm","D47.Z2"
> "0111157","Castleman disease","mesh","C536362"
> "0111157","Castleman disease","mesh","D005871"
> "0111157","Castleman disease","umls","C0017531"
> "0111157","Castleman disease","umls","C2931179"
> "0111157","Castleman disease","mondo","0015564"
> "0111150","autosomal dominant isolated ectopia lentis 1","mesh","C536184"
> "0111150","autosomal dominant isolated ectopia lentis 1","umls","C1851286"
> "0111150","autosomal dominant isolated ectopia lentis 1","mondo","0007514"
> "0111151","Prinzmetal angina","mesh","D000788"
> "0111151","Prinzmetal angina","mondo","0006021"
> "0111152","multicentric Castleman disease","mesh","C537372"
> "0111152","multicentric Castleman disease","umls","C1334815"
> "0111152","multicentric Castleman disease","mondo","0019754"
> "0111153","congenital mirror movement disorder","mondo","0016558"
> "0110683","congenital myasthenic syndrome 18","mondo","0014590"
> "0110682","congenital myasthenic syndrome 16","mondo","0013620"
> "0110681","congenital myasthenic syndrome 2A","mondo","0014581"
> "0110680","congenital myasthenic syndrome 2C","mondo","0014582"
> "0050648","atelosteogenesis","mondo","0000389"
> "0050649","atransferrinemia","mondo","0008846"
> "5048","posterior pituitary gland neoplasm","umls","C1334957"
> "5048","posterior pituitary gland neoplasm","mondo","0003257"
> "5047","neurohypophysis granular cell tumor","umls","C1333873"
> "5047","neurohypophysis granular cell tumor","mondo","0003256"
> "5046","mediastinal granular cell myoblastoma","umls","C1334656"
> "5046","mediastinal granular cell myoblastoma","mondo","0003255"
> "0050642","hypochromic microcytic anemia","mondo","0000387"
> "5044","cardiac granular cell neoplasm","umls","C1332845"
> "5044","cardiac granular cell neoplasm","mondo","0003254"
> "5043","vulvar granular cell tumor","umls","C1520083"
> "5043","vulvar granular cell tumor","mondo","0003253"
> "5042","malignant granular cell myoblastoma","umls","C0334618"
> "5042","malignant granular cell myoblastoma","mondo","0003252"
> "5041","esophageal cancer","icd10cm","C15.3"
> "5041","esophageal cancer","icd10cm","C15.4"
> "5041","esophageal cancer","icd10cm","C15.5"
> "5041","esophageal cancer","icd9cm","150.2"
> "5041","esophageal cancer","icd9cm","150.3"
> "5041","esophageal cancer","icd9cm","150.4"
> "5041","esophageal cancer","icd9cm","150.5"
> "5041","esophageal cancer","icd9cm","150.8"
> "5041","esophageal cancer","mesh","D004938"
> "5041","esophageal cancer","umls","C0014859"
> "5041","esophageal cancer","umls","C0153413"
> "5041","esophageal cancer","umls","C0153414"
> "5041","esophageal cancer","umls","C0153415"
> "5041","esophageal cancer","umls","C0153416"
> "5041","esophageal cancer","umls","C0496775"
> "5041","esophageal cancer","mondo","0007576"
> "5040","malignant granular cell esophageal tumor","umls","C1333448"
> "5040","malignant granular cell esophageal tumor","mondo","0003251"
> "0111486","combined oxidative phosphorylation deficiency 3","mesh","C566467"
> "0111486","combined oxidative phosphorylation deficiency 3","umls","C1864840"
> "10772","thrombotic thrombocytopenic purpura","icd10cm","M31.1"
> "10772","thrombotic thrombocytopenic purpura","mesh","D011697"
> "10772","thrombotic thrombocytopenic purpura","umls","C0034155"
> "10772","thrombotic thrombocytopenic purpura","mondo","0018896"
> "10773","bubonic plague","icd10cm","A20.0"
> "10773","bubonic plague","icd9cm","020.0"
> "10773","bubonic plague","mesh","D010930"
> "10773","bubonic plague","umls","C0282312"
> "10773","bubonic plague","mondo","0001112"
> "9513","plasma cell leukemia","icd10cm","C90.1"
> "9513","plasma cell leukemia","icd10cm","C90.10"
> "9513","plasma cell leukemia","icd9cm","203.1"
> "9513","plasma cell leukemia","mesh","D007952"
> "9513","plasma cell leukemia","umls","C0023484"
> "9513","plasma cell leukemia","mondo","0018689"
> "9512","simple chronic conjunctivitis","icd10cm","H10.42"
> "9512","simple chronic conjunctivitis","icd9cm","372.11"
> "9512","simple chronic conjunctivitis","umls","C0155146"
> "9512","simple chronic conjunctivitis","mondo","0004811"
> "0111371","isolated hyperchlorhidrosis","umls","C1840437"
> "10778","fiedler's myocarditis","icd10cm","I40.1"
> "10778","fiedler's myocarditis","icd9cm","422.91"
> "10778","fiedler's myocarditis","umls","C0155689"
> "10778","fiedler's myocarditis","mondo","0001113"
> "10779","septic myocarditis","icd10cm","I40.0"
> "10779","septic myocarditis","icd9cm","422.92"
> "10779","septic myocarditis","umls","C0155690"
> "10779","septic myocarditis","mondo","0001114"
> "0111374","selective pituitary thyroid hormone resistance","mesh","C564154"
> "0111374","selective pituitary thyroid hormone resistance","umls","C1840364"
> "0111375","fetal akinesia deformation sequence syndrome","mesh","C536647"
> "0111375","fetal akinesia deformation sequence syndrome","umls","C1276035"
> "11829","degenerative myopia","icd10cm","H44.2"
> "11829","degenerative myopia","icd9cm","360.21"
> "11829","degenerative myopia","mesh","D047728"
> "11829","degenerative myopia","umls","C0154778"
> "11829","degenerative myopia","mondo","0001383"
> "14679","VACTERL association","icd10cm","Q87.2"
> "14679","VACTERL association","mesh","C536534"
> "14679","VACTERL association","umls","C0220708"
> "14679","VACTERL association","mondo","0008642"
> "11824","multicentric reticulohistiocytosis","icd10cm","E78.81"
> "11824","multicentric reticulohistiocytosis","umls","C0311284"
> "11824","multicentric reticulohistiocytosis","mondo","0015347"
> "11821","bladder lymphoma","umls","C1332561"
> "11821","bladder lymphoma","mondo","0001381"
> "11820","bladder dome cancer","icd10cm","C67.1"
> "11820","bladder dome cancer","icd9cm","188.1"
> "11820","bladder dome cancer","umls","C0496827"
> "11820","bladder dome cancer","mondo","0001380"
> "11823","hepatorenal syndrome","icd10cm","K76.7"
> "11823","hepatorenal syndrome","icd9cm","572.4"
> "11823","hepatorenal syndrome","mesh","D006530"
> "11823","hepatorenal syndrome","umls","C0019212"
> "11823","hepatorenal syndrome","mondo","0001382"
> "14670","hypertelorism, microtia, facial clefting syndrome","mesh","C537632"
> "14670","hypertelorism, microtia, facial clefting syndrome","umls","C0220742"
> "14670","hypertelorism, microtia, facial clefting syndrome","mondo","0009404"
> "13089","intracranial arterial disease","mesh","D020765"
> "13089","intracranial arterial disease","umls","C0752138"
> "13089","intracranial arterial disease","mondo","0006808"
> "13088","periventricular leukomalacia","icd10cm","P91.2"
> "13088","periventricular leukomalacia","icd9cm","779.7"
> "13088","periventricular leukomalacia","mesh","D007969"
> "13088","periventricular leukomalacia","umls","C0023529"
> "13088","periventricular leukomalacia","mondo","0015742"
> "13087","Lown-Ganong-Levine syndrome","icd10cm","I45.6"
> "13087","Lown-Ganong-Levine syndrome","icd9cm","426.81"
> "13087","Lown-Ganong-Levine syndrome","mesh","D008151"
> "13087","Lown-Ganong-Levine syndrome","umls","C0024054"
> "13087","Lown-Ganong-Levine syndrome","mondo","0007174"
> "13081","hemangioma of subcutaneous tissue","umls","C0685200"
> "13081","hemangioma of subcutaneous tissue","mondo","0006557"
> "13080","Jaccoud's syndrome","icd10cm","M12.0"
> "13080","Jaccoud's syndrome","icd10cm","M12.00"
> "13080","Jaccoud's syndrome","icd9cm","714.4"
> "13080","Jaccoud's syndrome","umls","C0152084"
> "13080","Jaccoud's syndrome","mondo","0001629"
> "1357","maxillary sinus cancer","icd10cm","C31.0"
> "1357","maxillary sinus cancer","icd9cm","160.2"
> "1357","maxillary sinus cancer","umls","C0153476"
> "1357","maxillary sinus cancer","umls","C0740487"
> "1357","maxillary sinus cancer","mondo","0001748"
> "2425","cutaneous ganglioneuroma","umls","C0346063"
> "2425","cutaneous ganglioneuroma","mondo","0002293"
> "1252","trichuriasis","icd10cm","B79"
> "1252","trichuriasis","icd9cm","127.3"
> "1252","trichuriasis","mesh","D014257"
> "1252","trichuriasis","umls","C0040954"
> "1252","trichuriasis","mondo","0005996"
> "12797","hallucinogen abuse","icd10cm","F16.1"
> "12797","hallucinogen abuse","icd9cm","305.3"
> "12797","hallucinogen abuse","umls","C0018526"
> "12797","hallucinogen abuse","mondo","0001585"
> "1623","breast leiomyoma","umls","C1511317"
> "1623","breast leiomyoma","mondo","0002057"
> "5183","hereditary Wilms' tumor","umls","C0677779"
> "5183","hereditary Wilms' tumor","mondo","0003321"
> "1523","colon lymphoma","umls","C0519037"
> "1523","colon lymphoma","mondo","0002035"
> "1993","rectum cancer","icd10cm","C20"
> "1993","rectum cancer","icd9cm","154.1"
> "1993","rectum cancer","mesh","D012004"
> "1993","rectum cancer","umls","C0007113"
> "1993","rectum cancer","umls","C0949022"
> "1993","rectum cancer","mondo","0006519"
> "1992","rectum malignant melanoma","umls","C0349539"
> "1992","rectum malignant melanoma","mondo","0002167"
> "1995","rectum sarcoma","umls","C1335688"
> "1995","rectum sarcoma","mondo","0002168"
> "1626","breast duct papilloma","umls","C0238034"
> "1626","breast duct papilloma","mondo","0021097"
> "10194","kidney lipoma","umls","C1335744"
> "10194","kidney lipoma","mondo","0000968"
> "10195","pleural lipoma","umls","C1335434"
> "10195","pleural lipoma","mondo","0000969"
> "10192","pleomorphic lipoma","mesh","D008067"
> "10192","pleomorphic lipoma","umls","C0205823"
> "10192","pleomorphic lipoma","mondo","0000966"
> "1625","breast adenoma","umls","C1328385"
> "1625","breast adenoma","mondo","0002058"
> "10190","liver lipoma","umls","C1333970"
> "10190","liver lipoma","mondo","0000965"
> "3200","cerebellopontine angle tumor","mondo","0002553"
> "10199","breast lipoma","umls","C0349565"
> "10199","breast lipoma","mondo","0000970"
> "0110355","retinitis pigmentosa 32","icd10cm","H35.5"
> "0110355","retinitis pigmentosa 32","mondo","0012363"
> "0110354","retinitis pigmentosa 19","icd10cm","H35.5"
> "0110354","retinitis pigmentosa 19","mondo","0011137"
> "0110357","retinitis pigmentosa 35","icd10cm","H35.5"
> "0110357","retinitis pigmentosa 35","mondo","0012463"
> "0110356","retinitis pigmentosa 18","icd10cm","H35.5"
> "0110356","retinitis pigmentosa 18","mondo","0011075"
> "0110351","osteogenesis imperfecta type 11","icd10cm","Q78.0"
> "0110351","osteogenesis imperfecta type 11","mondo","0012592"
> "0110350","osteogenesis imperfecta type 6","icd10cm","Q78.0"
> "0110350","osteogenesis imperfecta type 6","mondo","0013515"
> "0110353","retinitis pigmentosa 20","icd10cm","H35.5"
> "0110353","retinitis pigmentosa 20","mondo","0013425"
> "0110352","retinitis pigmentosa 59","icd10cm","H35.5"
> "0110352","retinitis pigmentosa 59","mondo","0013468"
> "0110359","retinitis pigmentosa 67","icd10cm","H35.5"
> "0110359","retinitis pigmentosa 67","mondo","0014256"
> "0110358","retinitis pigmentosa 12","icd10cm","H35.5"
> "0110358","retinitis pigmentosa 12","mondo","0010818"
> "0110429","dilated cardiomyopathy 1H","icd10cm","I42.0"
> "0110429","dilated cardiomyopathy 1H","mondo","0011425"
> "0110428","dilated cardiomyopathy 1AA","icd10cm","I42.0"
> "0110428","dilated cardiomyopathy 1AA","mondo","0012808"
> "1129","pituitary apoplexy","mesh","D010899"
> "1129","pituitary apoplexy","umls","C0032001"
> "1129","pituitary apoplexy","mondo","0006908"
> "1628","intraductal papillary breast neoplasm","umls","C1334252"
> "1628","intraductal papillary breast neoplasm","mondo","0002061"
> "1123","spondyloarthropathy","mesh","D025242"
> "1123","spondyloarthropathy","umls","C0949691"
> "1123","spondyloarthropathy","mondo","0005095"
> "10152","Meckel's diverticulum cancer","icd9cm","152.3"
> "10152","Meckel's diverticulum cancer","umls","C0153429"
> "10152","Meckel's diverticulum cancer","mondo","0000954"
> "0110544","autosomal dominant nonsyndromic deafness 12","icd10cm","H90.3"
> "0110544","autosomal dominant nonsyndromic deafness 12","mondo","0011102"
> "0110545","autosomal dominant nonsyndromic deafness 13","icd10cm","H90.3"
> "0110545","autosomal dominant nonsyndromic deafness 13","mondo","0011159"
> "0110546","autosomal dominant nonsyndromic deafness 15","icd10cm","H90.3"
> "0110546","autosomal dominant nonsyndromic deafness 15","mondo","0011226"
> "0060269","pontocerebellar hypoplasia type 2C","mesh","C567324"
> "0060269","pontocerebellar hypoplasia type 2C","umls","C2676465"
> "0060269","pontocerebellar hypoplasia type 2C","mondo","0012891"
> "0060268","pontocerebellar hypoplasia type 2B","mesh","C567325"
> "0060268","pontocerebellar hypoplasia type 2B","umls","C2676466"
> "0060268","pontocerebellar hypoplasia type 2B","mondo","0012890"
> "0110547","autosomal dominant nonsyndromic deafness 16","icd10cm","H90.3"
> "0110547","autosomal dominant nonsyndromic deafness 16","mondo","0011389"
> "0060261","congenital ptosis","icd10cm","Q10.0"
> "0060261","congenital ptosis","icd9cm","743.61"
> "0060261","congenital ptosis","umls","C0266573"
> "0060261","congenital ptosis","mondo","0008340"
> "0060260","ptosis","icd10cm","H02.4"
> "0060260","ptosis","icd10cm","H02.40"
> "0060260","ptosis","icd10cm","H02.409"
> "0060260","ptosis","icd9cm","374.3"
> "0060260","ptosis","icd9cm","374.30"
> "0060260","ptosis","mesh","D001763"
> "0060260","ptosis","umls","C0005745"
> "0060260","ptosis","mondo","0000728"
> "0060263","porencephaly","icd10cm","Q04.6"
> "0060263","porencephaly","mesh","D065708"
> "0060263","porencephaly","umls","C0302892"
> "0060263","porencephaly","umls","C1867983"
> "0060263","porencephaly","umls","C3698507"
> "0060263","porencephaly","mondo","0017410"
> "0060262","gallbladder disease","icd10cm","K82.9"
> "0060262","gallbladder disease","icd9cm","575.9"
> "0060262","gallbladder disease","mesh","D005705"
> "0060262","gallbladder disease","umls","C0016977"
> "0060262","gallbladder disease","mondo","0005281"
> "0060265","pontocerebellar hypoplasia type 1A","mondo","0011866"
> "0060264","pontocerebellar hypoplasia","mesh","C580383"
> "0060264","pontocerebellar hypoplasia","umls","C0266468"
> "0060264","pontocerebellar hypoplasia","mondo","0020135"
> "0060267","pontocerebellar hypoplasia type 2A","mesh","C564738"
> "0060267","pontocerebellar hypoplasia type 2A","umls","C1848526"
> "0060267","pontocerebellar hypoplasia type 2A","mondo","0010190"
> "0060266","pontocerebellar hypoplasia type 1B","mondo","0013853"
> "8516","pulmonary embolism and infarction","icd9cm","415.1"
> "8516","pulmonary embolism and infarction","umls","C0034066"
> "8516","pulmonary embolism and infarction","mondo","0004597"
> "8517","acute cor pulmonale","icd10cm","I26.09"
> "8517","acute cor pulmonale","icd9cm","415.0"
> "8517","acute cor pulmonale","umls","C0155672"
> "8517","acute cor pulmonale","mondo","0004598"
> "8042","testis polyembryoma","umls","C1514200"
> "8042","testis polyembryoma","mondo","0004442"
> "8515","Cor pulmonale","icd10cm","I27.81"
> "8515","Cor pulmonale","icd10cm","I27.9"
> "8515","Cor pulmonale","mesh","D011660"
> "8515","Cor pulmonale","umls","C0034072"
> "8515","Cor pulmonale","mondo","0004596"
> "8512","puerperal pulmonary embolism","icd10cm","O88.21"
> "8512","puerperal pulmonary embolism","icd10cm","O88.23"
> "8512","puerperal pulmonary embolism","icd9cm","673"
> "8512","puerperal pulmonary embolism","umls","C0157540"
> "8512","puerperal pulmonary embolism","mondo","0004594"
> "0110542","autosomal dominant nonsyndromic deafness 10","icd10cm","H90.3"
> "0110542","autosomal dominant nonsyndromic deafness 10","mondo","0011031"
> "0110543","autosomal dominant nonsyndromic deafness 11","icd10cm","H90.3"
> "0110543","autosomal dominant nonsyndromic deafness 11","mondo","0011032"
> "8519","barbiturate abuse","icd10cm","F13.11"
> "8519","barbiturate abuse","icd9cm","305.43"
> "8519","barbiturate abuse","umls","C0154529"
> "8519","barbiturate abuse","mondo","0004599"
> "12849","autistic disorder","icd10cm","F84.0"
> "12849","autistic disorder","icd9cm","299.0"
> "12849","autistic disorder","mesh","D001321"
> "12849","autistic disorder","umls","C0004352"
> "12849","autistic disorder","mondo","0005260"
> "12842","Guillain-Barre syndrome","icd10cm","G61.0"
> "12842","Guillain-Barre syndrome","mesh","D020275"
> "12842","Guillain-Barre syndrome","umls","C0018378"
> "12842","Guillain-Barre syndrome","mondo","0016218"
> "12841","ancylostomiasis","icd10cm","B76.0"
> "12841","ancylostomiasis","mesh","D000724"
> "12841","ancylostomiasis","umls","C0002831"
> "12841","ancylostomiasis","mondo","0005645"
> "0060046","aphasia","mesh","D001037"
> "0060046","aphasia","mondo","0000598"
> "0060041","autism spectrum disorder","mesh","D000067877"
> "0060041","autism spectrum disorder","mondo","0005258"
> "0060040","pervasive developmental disorder","icd9cm","299.80"
> "0060040","pervasive developmental disorder","umls","C0154451"
> "0060040","pervasive developmental disorder","mondo","0000594"
> "13575","non-renal secondary hyperparathyroidism","icd9cm","252.02"
> "13575","non-renal secondary hyperparathyroidism","umls","C1456268"
> "13575","non-renal secondary hyperparathyroidism","mondo","0001750"
> "0080209","sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay","mondo","0014487"
> "0080208","non-alcoholic fatty liver disease","mondo","0013209"
> "0080205","CAKUT","mondo","0019719"
> "0080204","renal hypoplasia","mondo","0019637"
> "0080207","CAKUT2","mondo","0027676"
> "0080206","CAKUT1","mondo","0012561"
> "0080201","Peters plus syndrome","mondo","0009856"
> "0080200","bilateral renal aplasia","mondo","0015986"
> "0080202","adenoid cystic carcinoma","mesh","D003528"
> "0080202","adenoid cystic carcinoma","mondo","0004971"
> "4776","rapidly progressive glomerulonephritis","icd10cm","N01"
> "4776","rapidly progressive glomerulonephritis","umls","C0221239"
> "4776","rapidly progressive glomerulonephritis","mondo","0017236"
> "4777","exudative glomerulonephritis","umls","C0546345"
> "4777","exudative glomerulonephritis","mondo","0003133"
> "4772","mesoblastic nephroma","mesh","D018201"
> "4772","mesoblastic nephroma","umls","C0206628"
> "4772","mesoblastic nephroma","mondo","0003130"
> "4773","congenital mesoblastic nephroma","mesh","D018201"
> "4773","congenital mesoblastic nephroma","umls","C1332965"
> "4773","congenital mesoblastic nephroma","mondo","0017043"
> "13641","exfoliation syndrome","icd9cm","365.52"
> "13641","exfoliation syndrome","mesh","D017889"
> "13641","exfoliation syndrome","umls","C0206368"
> "13641","exfoliation syndrome","mondo","0008327"
> "4778","proliferative glomerulonephritis","umls","C0235618"
> "4778","proliferative glomerulonephritis","mondo","0003134"
> "4779","focal embolic glomerulonephritis","umls","C0238143"
> "4779","focal embolic glomerulonephritis","mondo","0003135"
> "14711","FG syndrome","mesh","C537923"
> "14711","FG syndrome","umls","C0220769"
> "14711","FG syndrome","mondo","0002010"
> "5810","adenosine deaminase deficiency","icd10cm","D81.3"
> "5810","adenosine deaminase deficiency","umls","C0268124"
> "5810","adenosine deaminase deficiency","mondo","0007064"
> "5812","MHC class II deficiency","icd10cm","D81.6"
> "5812","MHC class II deficiency","mesh","D016511"
> "5812","MHC class II deficiency","umls","C0242583"
> "5812","MHC class II deficiency","mondo","0008855"
> "5813","purine nucleoside phosphorylase deficiency","icd10cm","D81.5"
> "5813","purine nucleoside phosphorylase deficiency","mesh","C562587"
> "5813","purine nucleoside phosphorylase deficiency","umls","C0268125"
> "5813","purine nucleoside phosphorylase deficiency","mondo","0013171"
> "5815","cerebral lymphoma","umls","C0240803"
> "5815","cerebral lymphoma","mondo","0003655"
> "14243","chronic perichondritis of pinna","icd9cm","380.02"
> "14243","chronic perichondritis of pinna","umls","C0155391"
> "14243","chronic perichondritis of pinna","mondo","0001917"
> "4618","maxillary cancer","mesh","D008441"
> "4618","maxillary cancer","umls","C0024954"
> "4618","maxillary cancer","mondo","0005841"
> "13500","hairy tongue","mesh","D014064"
> "13500","hairy tongue","umls","C0040414"
> "13500","hairy tongue","mondo","0006777"
> "4610","intestinal benign neoplasm","mesh","D007414"
> "4610","intestinal benign neoplasm","umls","C0021841"
> "4610","intestinal benign neoplasm","mondo","0021118"
> "4613","ulnar neuropathy","mesh","D020424"
> "4613","ulnar neuropathy","umls","C0154743"
> "4613","ulnar neuropathy","mondo","0007006"
> "4617","periapical granuloma","mesh","D010484"
> "4617","periapical granuloma","umls","C0031029"
> "4617","periapical granuloma","mondo","0006897"
> "13507","trigonitis","icd10cm","N30.3"
> "13507","trigonitis","icd9cm","595.3"
> "13507","trigonitis","umls","C1261278"
> "13507","trigonitis","mondo","0001732"
> "5063","basosquamous carcinoma","mesh","D002281"
> "5063","basosquamous carcinoma","umls","C0007118"
> "5063","basosquamous carcinoma","mondo","0003264"
> "2705","malignant giant cell tumor","umls","C0334229"
> "2705","malignant giant cell tumor","mondo","0002402"
> "146","papilledema","icd10cm","H46.0"
> "146","papilledema","icd10cm","H47.1"
> "146","papilledema","icd10cm","H47.10"
> "146","papilledema","icd9cm","377.0"
> "146","papilledema","icd9cm","377.00"
> "146","papilledema","icd9cm","377.31"
> "146","papilledema","mesh","D010211"
> "146","papilledema","umls","C0030353"
> "146","papilledema","mondo","0002003"
> "2700","mucinous adenofibroma","umls","C0334499"
> "2700","mucinous adenofibroma","mondo","0002398"
> "10688","hypertrophy of breast","icd10cm","N62"
> "10688","hypertrophy of breast","icd9cm","611.1"
> "10688","hypertrophy of breast","umls","C0020565"
> "10688","hypertrophy of breast","mondo","0001100"
> "7967","lipid-cell variant infiltrating bladder urothelial carcinoma","umls","C1512738"
> "7967","lipid-cell variant infiltrating bladder urothelial carcinoma","mondo","0004415"
> "2712","phimosis","icd10cm","N47.1"
> "2712","phimosis","mesh","D010688"
> "2712","phimosis","umls","C0031538"
> "2712","phimosis","mondo","0006904"
> "2710","sick building syndrome","mesh","D018877"
> "2710","sick building syndrome","umls","C0037050"
> "2710","sick building syndrome","mondo","0005959"
> "3341","osteitis fibrosa","mesh","D010002"
> "3341","osteitis fibrosa","umls","C0029405"
> "3341","osteitis fibrosa","mondo","0005890"
> "2717","Bloom syndrome","mesh","D001816"
> "2717","Bloom syndrome","umls","C0005859"
> "2717","Bloom syndrome","mondo","0008876"
> "2718","hemopneumothorax","icd10cm","J94.2"
> "2718","hemopneumothorax","mesh","D006468"
> "2718","hemopneumothorax","umls","C0019077"
> "2718","hemopneumothorax","mondo","0006783"
> "7221","gallbladder papillary carcinoma","umls","C1333753"
> "7221","gallbladder papillary carcinoma","mondo","0004148"
> "7223","breast giant fibroadenoma","umls","C0346157"
> "7223","breast giant fibroadenoma","mondo","0004150"
> "10348","blepharophimosis","icd10cm","H02.52"
> "10348","blepharophimosis","icd9cm","374.46"
> "10348","blepharophimosis","mesh","D016569"
> "10348","blepharophimosis","umls","C0005744"
> "10348","blepharophimosis","mondo","0001008"
> "7953","nipple duct carcinoma","umls","C1334967"
> "7953","nipple duct carcinoma","mondo","0004409"
> "7224","spinal meninges cancer","icd10cm","C70.1"
> "7224","spinal meninges cancer","icd9cm","192.3"
> "7224","spinal meninges cancer","umls","C0153647"
> "7224","spinal meninges cancer","mondo","0004151"
> "7951","Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma","umls","C1516760"
> "7951","Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma","mondo","0004408"
> "0070128","congenital nongoitrous hypothyroidism 6","icd10cm","E03.1"
> "0070128","congenital nongoitrous hypothyroidism 6","mondo","0013757"
> "9164","achalasia","icd10cm","K22.0"
> "9164","achalasia","icd9cm","530.0"
> "9164","achalasia","mesh","D004931"
> "9164","achalasia","umls","C0014848"
> "9164","achalasia","mondo","0008698"
> "9165","neurotic excoriation","icd10cm","L98.1"
> "9165","neurotic excoriation","icd9cm","698.4"
> "9165","neurotic excoriation","umls","C1274184"
> "9165","neurotic excoriation","mondo","0006586"
> "0070125","congenital nongoitrous hypothyroidism 5","icd10cm","E03.1"
> "0070125","congenital nongoitrous hypothyroidism 5","mondo","0009154"
> "5457","laryngeal neuroendocrine tumor","umls","C1334374"
> "5457","laryngeal neuroendocrine tumor","mondo","0015070"
> "0070123","congenital nongoitrous hypothyroidism 4","icd10cm","E03.1"
> "0070123","congenital nongoitrous hypothyroidism 4","mondo","0010139"
> "0070136","autosomal dominant cutis laxa 2","icd10cm","Q82.8"
> "0070136","autosomal dominant cutis laxa 2","mondo","0009054"
> "0070121","Meckel syndrome 7","mesh","C537756"
> "0070121","Meckel syndrome 7","umls","C2673885"
> "0070121","Meckel syndrome 7","mondo","0009966"
> "0070120","Meckel syndrome 6","icd10cm","Q61.9"
> "0070120","Meckel syndrome 6","mondo","0012848"
> "0110168","Charcot-Marie-Tooth disease type 2Y","icd10cm","G60.0"
> "0110168","Charcot-Marie-Tooth disease type 2Y","mondo","0014735"
> "7969","nested variant infiltrating bladder urothelial carcinoma","umls","C1512741"
> "7969","nested variant infiltrating bladder urothelial carcinoma","mondo","0004417"
> "0110162","Charcot-Marie-Tooth disease, axonal type 2W","mondo","0014711"
> "9173","submandibular gland cancer","icd10cm","C08.0"
> "9173","submandibular gland cancer","icd9cm","142.1"
> "9173","submandibular gland cancer","umls","C0153360"
> "9173","submandibular gland cancer","mondo","0004724"
> "0110160","Charcot-Marie-Tooth disease axonal type 2T","icd10cm","G60.0"
> "0110160","Charcot-Marie-Tooth disease axonal type 2T","mondo","0014866"
> "0110161","Charcot-Marie-Tooth disease type 2R","icd10cm","G60.0"
> "0110161","Charcot-Marie-Tooth disease type 2R","mondo","0014208"
> "0110166","Charcot-Marie-Tooth disease axonal type 2H","icd10cm","G60.0"
> "0110166","Charcot-Marie-Tooth disease axonal type 2H","mondo","0011901"
> "0110167","Charcot-Marie-Tooth disease axonal type 2K","icd10cm","G60.0"
> "0110167","Charcot-Marie-Tooth disease axonal type 2K","mondo","0011916"
> "0110164","Charcot-Marie-Tooth disease type 2D","icd10cm","G60.0"
> "0110164","Charcot-Marie-Tooth disease type 2D","mondo","0011091"
> "0110165","Charcot-Marie-Tooth disease type 2E","icd10cm","G60.0"
> "0110165","Charcot-Marie-Tooth disease type 2E","mondo","0011894"
> "6249","mediastinum seminoma","umls","C1334680"
> "6249","mediastinum seminoma","mondo","0003826"
> "12271","aniridia","icd10cm","Q13.1"
> "12271","aniridia","icd9cm","743.45"
> "12271","aniridia","mesh","D015783"
> "12271","aniridia","umls","C0003076"
> "12271","aniridia","mondo","0019172"
> "12270","coloboma","icd10cm","Q13.0"
> "12270","coloboma","mesh","D003103"
> "12270","coloboma","umls","C0009363"
> "12270","coloboma","mondo","0001476"
> "12273","anisometropia","icd10cm","H52.31"
> "12273","anisometropia","icd9cm","367.31"
> "12273","anisometropia","mesh","D015858"
> "12273","anisometropia","umls","C0003081"
> "12273","anisometropia","mondo","0001478"
> "6244","familial renal oncocytoma","umls","C0879606"
> "6244","familial renal oncocytoma","mondo","0003824"
> "6245","renal oncocytoma","mesh","C537750"
> "6245","renal oncocytoma","umls","C0346255"
> "6245","renal oncocytoma","mondo","0003825"
> "12276","malignant tumor of undescended testis","icd10cm","C62.0"
> "12276","malignant tumor of undescended testis","icd9cm","186.0"
> "12276","malignant tumor of undescended testis","umls","C0153595"
> "12276","malignant tumor of undescended testis","mondo","0001480"
> "10525","double pterygium","icd9cm","372.44"
> "10525","double pterygium","umls","C0155157"
> "10525","double pterygium","mondo","0001054"
> "10520","acute infection of pinna","icd9cm","380.11"
> "10520","acute infection of pinna","umls","C0155392"
> "10520","acute infection of pinna","mondo","0001053"
> "7927","malignant type A thymoma","umls","C0279707"
> "7927","malignant type A thymoma","mondo","0004400"
> "9709","rosacea conjunctivitis","icd9cm","372.31"
> "9709","rosacea conjunctivitis","umls","C0155152"
> "9709","rosacea conjunctivitis","mondo","0004856"
> "9700","bacterial conjunctivitis","icd10cm","H10.0"
> "9700","bacterial conjunctivitis","mesh","D003234"
> "9700","bacterial conjunctivitis","umls","C0009768"
> "9700","bacterial conjunctivitis","mondo","0006668"
> "8872","penis carcinoma in situ","icd10cm","D00-D09"
> "8872","penis carcinoma in situ","icd10cm","D07.4"
> "8872","penis carcinoma in situ","icd9cm","233.5"
> "8872","penis carcinoma in situ","umls","C0154089"
> "8872","penis carcinoma in situ","mondo","0004671"
> "824","periodontitis","icd10cm","K05.3"
> "824","periodontitis","mesh","D010518"
> "824","periodontitis","umls","C0031099"
> "824","periodontitis","mondo","0005076"
> "827","ureter tuberculosis","icd9cm","016.2"
> "827","ureter tuberculosis","umls","C0152800"
> "827","ureter tuberculosis","mondo","0004517"
> "820","myocarditis","kegg","05416"
> "820","myocarditis","icd10cm","I51.4"
> "820","myocarditis","icd9cm","429.0"
> "820","myocarditis","mesh","D009205"
> "820","myocarditis","umls","C0027059"
> "820","myocarditis","mondo","0004496"
> "823","periapical periodontitis","icd10cm","K04.5"
> "823","periapical periodontitis","mesh","D010485"
> "823","periapical periodontitis","umls","C0031030"
> "823","periapical periodontitis","mondo","0004508"
> "12491","Vagus nerve disease","icd10cm","G52.2"
> "12491","Vagus nerve disease","icd9cm","352.3"
> "12491","Vagus nerve disease","mesh","D020421"
> "12491","Vagus nerve disease","umls","C0152179"
> "12491","Vagus nerve disease","mondo","0001535"
> "13316","exocrine pancreatic insufficiency","icd10cm","K86.81"
> "13316","exocrine pancreatic insufficiency","mesh","D010188"
> "13316","exocrine pancreatic insufficiency","umls","C0267963"
> "13316","exocrine pancreatic insufficiency","mondo","0001684"
> "12637","perineocele","icd10cm","N81.81"
> "12637","perineocele","icd9cm","618.05"
> "12637","perineocele","umls","C1456251"
> "12637","perineocele","mondo","0001559"
> "6977","pancreatic cholera","mesh","D003969"
> "6977","pancreatic cholera","umls","C0086768"
> "6977","pancreatic cholera","mondo","0004058"
> "12639","pyloric stenosis","icd10cm","K31.1"
> "12639","pyloric stenosis","mesh","D011707"
> "12639","pyloric stenosis","umls","C0034194"
> "12639","pyloric stenosis","mondo","0001561"
> "1713","benign shuddering attacks","icd10cm","G25.83"
> "1713","benign shuddering attacks","icd9cm","333.93"
> "1713","benign shuddering attacks","umls","C0375200"
> "1713","benign shuddering attacks","mondo","0002085"
> "1712","aortic valve stenosis","mesh","D001024"
> "1712","aortic valve stenosis","umls","C0003507"
> "1712","aortic valve stenosis","umls","C0152417"
> "1712","aortic valve stenosis","umls","C0155567"
> "1712","aortic valve stenosis","mondo","0004978"
> "5251","inflammatory leiomyosarcoma","umls","C1334179"
> "5251","inflammatory leiomyosarcoma","mondo","0003347"
> "5254","central nervous system leiomyosarcoma","umls","C1334385"
> "5254","central nervous system leiomyosarcoma","mondo","0003349"
> "14192","bicipital tenosynovitis","icd9cm","726.12"
> "14192","bicipital tenosynovitis","umls","C0158304"
> "14192","bicipital tenosynovitis","mondo","0001905"
> "5258","granular cell leiomyosarcoma","umls","C1333871"
> "5258","granular cell leiomyosarcoma","mondo","0003350"
> "5259","colon leiomyosarcoma","umls","C1333093"
> "5259","colon leiomyosarcoma","mondo","0003351"
> "13941","benign paroxysmal positional nystagmus","icd9cm","386.11"
> "13941","benign paroxysmal positional nystagmus","mesh","D065635"
> "13941","benign paroxysmal positional nystagmus","umls","C0155502"
> "13941","benign paroxysmal positional nystagmus","mondo","0008656"
> "13942","acute gonococcal salpingitis","icd9cm","098.17"
> "13942","acute gonococcal salpingitis","umls","C0275654"
> "13942","acute gonococcal salpingitis","mondo","0001837"
> "13943","acute gonococcal prostatitis","icd9cm","098.12"
> "13943","acute gonococcal prostatitis","umls","C0153192"
> "13943","acute gonococcal prostatitis","mondo","0001838"
> "11638","presbyopia","icd10cm","H52.4"
> "11638","presbyopia","icd9cm","367.4"
> "11638","presbyopia","mesh","D011305"
> "11638","presbyopia","umls","C0033075"
> "11638","presbyopia","mondo","0001330"
> "13945","CADASIL","mesh","D046589"
> "13945","CADASIL","umls","C0751587"
> "13945","CADASIL","mondo","0007432"
> "11120","psychologic dyspareunia","icd10cm","F52.6"
> "11120","psychologic dyspareunia","icd9cm","302.76"
> "11120","psychologic dyspareunia","umls","C0154466"
> "11120","psychologic dyspareunia","mondo","0001196"
> "11121","pulpitis","icd10cm","K04.0"
> "11121","pulpitis","icd9cm","522.0"
> "11121","pulpitis","mesh","D011671"
> "11121","pulpitis","umls","C0034103"
> "11121","pulpitis","mondo","0006937"
> "11123","Henoch-Schoenlein purpura","icd10cm","D69.0"
> "11123","Henoch-Schoenlein purpura","icd9cm","287.0"
> "11123","Henoch-Schoenlein purpura","mesh","D011695"
> "11123","Henoch-Schoenlein purpura","umls","C0034152"
> "11123","Henoch-Schoenlein purpura","mondo","0006785"
> "14332","postencephalitic Parkinson disease","icd10cm","G21.3"
> "14332","postencephalitic Parkinson disease","mesh","D010301"
> "14332","postencephalitic Parkinson disease","umls","C0030568"
> "14332","postencephalitic Parkinson disease","mondo","0001945"
> "11125","qualitative platelet defect","icd10cm","D69.1"
> "11125","qualitative platelet defect","icd9cm","287.1"
> "11125","qualitative platelet defect","umls","C0235604"
> "11125","qualitative platelet defect","mondo","0001197"
> "11126","acquired thrombocytopenia","icd10cm","D69.5"
> "11126","acquired thrombocytopenia","icd9cm","287.4"
> "11126","acquired thrombocytopenia","umls","C0154301"
> "11126","acquired thrombocytopenia","mondo","0001198"
> "14447","gonadal dysgenesis","icd9cm","758.6"
> "14447","gonadal dysgenesis","mesh","D006059"
> "14447","gonadal dysgenesis","umls","C0018051"
> "14447","gonadal dysgenesis","mondo","0001967"
> "14448","46 XY gonadal dysgenesis","mesh","D006061"
> "14448","46 XY gonadal dysgenesis","umls","C0018054"
> "14448","46 XY gonadal dysgenesis","mondo","0010765"
> "11129","dislocation of ear ossicle","icd9cm","385.23"
> "11129","dislocation of ear ossicle","umls","C0155487"
> "11129","dislocation of ear ossicle","mondo","0001199"
> "3012","Li-Fraumeni syndrome","mesh","D016864"
> "3012","Li-Fraumeni syndrome","umls","C0085390"
> "3012","Li-Fraumeni syndrome","mondo","0018875"
> "3013","intraductal breast neoplasm","umls","C0948967"
> "3013","intraductal breast neoplasm","mondo","0002488"
> "3010","lobular neoplasia","umls","C0861352"
> "3010","lobular neoplasia","mondo","0002486"
> "3011","breast granular cell tumor","umls","C1511312"
> "3011","breast granular cell tumor","mondo","0002487"
> "3016","breast malignant phyllodes tumor","mesh","D003557"
> "3016","breast malignant phyllodes tumor","umls","C0238031"
> "3016","breast malignant phyllodes tumor","umls","C0346154"
> "3016","breast malignant phyllodes tumor","umls","C0600066"
> "3016","breast malignant phyllodes tumor","mondo","0002489"
> "3017","breast sarcoma","umls","C0349667"
> "3017","breast sarcoma","mondo","0002490"
> "8729","milker's nodule","icd10cm","B08.04"
> "8729","milker's nodule","icd9cm","051.1"
> "8729","milker's nodule","icd9cm","051.9"
> "8729","milker's nodule","mesh","D011213"
> "8729","milker's nodule","umls","C0026143"
> "8729","milker's nodule","mondo","0005850"
> "8725","vascular dementia","icd10cm","F01"
> "8725","vascular dementia","icd10cm","F01.5"
> "8725","vascular dementia","icd9cm","290.4"
> "8725","vascular dementia","mesh","D015140"
> "8725","vascular dementia","mesh","D015161"
> "8725","vascular dementia","umls","C0011263"
> "8725","vascular dementia","umls","C0011269"
> "8725","vascular dementia","mondo","0004648"
> "4189","mutism","mesh","D009155"
> "4189","mutism","umls","C0026884"
> "4189","mutism","mondo","0002905"
> "4188","echolalia","mesh","D004454"
> "4188","echolalia","umls","C0013528"
> "4188","echolalia","mondo","0002904"
> "7921","benign mediastinal psammomatous neurilemmoma","umls","C1332513"
> "7921","benign mediastinal psammomatous neurilemmoma","mondo","0004397"
> "0060458","chromosome 2q31.1 duplication syndrome","mondo","0013363"
> "0060459","chromosome 3q29 microduplication syndrome","icd10cm","Q92.3"
> "0060459","chromosome 3q29 microduplication syndrome","mesh","C567626"
> "0060459","chromosome 3q29 microduplication syndrome","mondo","0012761"
> "0060456","Schnyder corneal dystrophy","mesh","C535475"
> "0060456","Schnyder corneal dystrophy","umls","C0271287"
> "0060456","Schnyder corneal dystrophy","mondo","0007374"
> "0060457","posterior polymorphous corneal dystrophy","icd10cm","H18.5"
> "0060457","posterior polymorphous corneal dystrophy","mesh","C562745"
> "0060457","posterior polymorphous corneal dystrophy","mondo","0020364"
> "4183","pseudopseudohypoparathyroidism","mesh","D011556"
> "4183","pseudopseudohypoparathyroidism","umls","C0033835"
> "4183","pseudopseudohypoparathyroidism","mondo","0012912"
> "0060455","Thiel-Behnke corneal dystrophy","mesh","C535942"
> "0060455","Thiel-Behnke corneal dystrophy","umls","C1562894"
> "0060455","Thiel-Behnke corneal dystrophy","mondo","0011185"
> "0060452","posterior amorphous corneal dystrophy","icd10cm","H18.5"
> "0060452","posterior amorphous corneal dystrophy","mesh","C567546"
> "0060452","posterior amorphous corneal dystrophy","mondo","0013027"
> "0060453","Reis-Bucklers corneal dystrophy","mesh","C535476"
> "0060453","Reis-Bucklers corneal dystrophy","umls","C0339278"
> "0060453","Reis-Bucklers corneal dystrophy","mondo","0012043"
> "0060450","Lisch epithelial corneal dystrophy","icd10cm","H18.5"
> "0060450","Lisch epithelial corneal dystrophy","mesh","C567588"
> "0060450","Lisch epithelial corneal dystrophy","mondo","0010425"
> "0060451","Meesmann corneal dystrophy","icd10cm","H18.52"
> "0060451","Meesmann corneal dystrophy","icd9cm","371.51"
> "0060451","Meesmann corneal dystrophy","mesh","D053559"
> "0060451","Meesmann corneal dystrophy","umls","C0339277"
> "0060451","Meesmann corneal dystrophy","mondo","0007379"
> "5662","pleomorphic carcinoma","umls","C0334233"
> "5662","pleomorphic carcinoma","mondo","0003573"
> "5660","lymphoepithelioma-like carcinoma","umls","C0334254"
> "5660","lymphoepithelioma-like carcinoma","mondo","0003572"
> "5667","sweat gland carcinoma","umls","C1412016"
> "5667","sweat gland carcinoma","mondo","0005524"
> "5665","external ear cancer","umls","C0349576"
> "5665","external ear cancer","mondo","0003574"
> "14683","Binder syndrome","mesh","C536036"
> "14683","Binder syndrome","umls","C0220692"
> "14683","Binder syndrome","mondo","0007953"
> "10203","external auditory meatus lipoma","umls","C0347423"
> "10203","external auditory meatus lipoma","mondo","0000973"
> "10330","slate pneumoconiosis","umls","C0340186"
> "10330","slate pneumoconiosis","mondo","0001004"
> "6406","double outlet right ventricle","icd10cm","Q20.1"
> "6406","double outlet right ventricle","icd9cm","745.11"
> "6406","double outlet right ventricle","mesh","D004310"
> "6406","double outlet right ventricle","umls","C0013069"
> "6406","double outlet right ventricle","mondo","0018089"
> "8188","uterine corpus choriocarcinoma","umls","C1336904"
> "8188","uterine corpus choriocarcinoma","mondo","0004491"
> "6404","metanephric adenoma","umls","C1266045"
> "6404","metanephric adenoma","mondo","0006301"
> "6405","ovarian papillary cystadenoma","umls","C1335175"
> "6405","ovarian papillary cystadenoma","mondo","0003872"
> "18","urinary system disease","umls","C1335051"
> "18","urinary system disease","mondo","0002118"
> "6408","ovary papillary carcinoma","umls","C1335178"
> "6408","ovary papillary carcinoma","mondo","0003874"
> "8186","fallopian tube gestational choriocarcinoma","umls","C1333593"
> "8186","fallopian tube gestational choriocarcinoma","mondo","0004489"
> "7764","subglottis carcinoma","umls","C1299239"
> "7764","subglottis carcinoma","mondo","0004358"
> "7765","Coats disease","icd10cm","H35.02"
> "7765","Coats disease","icd10cm","H35.07"
> "7765","Coats disease","icd9cm","362.12"
> "7765","Coats disease","mesh","D058456"
> "7765","Coats disease","umls","C0154832"
> "7765","Coats disease","mondo","0010269"
> "7762","childhood multilocular cystic kidney neoplasm","umls","C1332983"
> "7762","childhood multilocular cystic kidney neoplasm","mondo","0004356"
> "7763","carcinoma of supraglottis","umls","C1299240"
> "7763","carcinoma of supraglottis","mondo","0004357"
> "3904","bronchus carcinoma","mesh","D002283"
> "3904","bronchus carcinoma","umls","C0007121"
> "3904","bronchus carcinoma","mondo","0002806"
> "3905","lung carcinoma","icd10cm","C34.90"
> "3905","lung carcinoma","umls","C0684249"
> "3905","lung carcinoma","mondo","0005138"
> "3906","bronchial neoplasm","mesh","D001984"
> "3906","bronchial neoplasm","umls","C0006264"
> "3906","bronchial neoplasm","mondo","0002807"
> "3907","lung squamous cell carcinoma","umls","C0149782"
> "3907","lung squamous cell carcinoma","mondo","0005097"
> "3901","vulvitis","icd10cm","N76.2"
> "3901","vulvitis","mesh","D014847"
> "3901","vulvitis","umls","C0042996"
> "3901","vulvitis","mondo","0007018"
> "3908","lung non-small cell carcinoma","kegg","05223"
> "3908","lung non-small cell carcinoma","mesh","D002289"
> "3908","lung non-small cell carcinoma","umls","C0007131"
> "3908","lung non-small cell carcinoma","mondo","0005233"
> "0110988","Joubert syndrome 2","mesh","C536294"
> "0110988","Joubert syndrome 2","mondo","0011963"
> "0110989","Joubert syndrome 20","mondo","0013994"
> "6742","synchronous bilateral breast carcinoma","umls","C1515107"
> "6742","synchronous bilateral breast carcinoma","mondo","0003983"
> "0110984","Joubert syndrome 15","mondo","0013763"
> "0110985","Joubert syndrome 16","mondo","0013764"
> "0110986","Joubert syndrome 17","mondo","0013824"
> "0110987","Joubert syndrome 18","mondo","0013896"
> "0110980","Joubert syndrome 1","mondo","0008944"
> "0110981","Joubert syndrome 10","mesh","C567582"
> "0110981","Joubert syndrome 10","mondo","0010431"
> "0110982","Joubert syndrome 13","mondo","0013608"
> "0110983","Joubert syndrome 14","mondo","0013745"
> "9958","hemometra","icd10cm","N85.7"
> "9958","hemometra","icd9cm","621.4"
> "9958","hemometra","mesh","D006409"
> "9958","hemometra","umls","C0018948"
> "9958","hemometra","mondo","0006782"
> "9955","hypoplastic left heart syndrome","icd10cm","Q23.4"
> "9955","hypoplastic left heart syndrome","icd9cm","746.7"
> "9955","hypoplastic left heart syndrome","mesh","D018636"
> "9955","hypoplastic left heart syndrome","umls","C0152101"
> "9955","hypoplastic left heart syndrome","mondo","0004933"
> "9954","null-cell leukemia","umls","C0023483"
> "9954","null-cell leukemia","mondo","0004932"
> "9957","periostitis","mesh","D010522"
> "9957","periostitis","umls","C0031111"
> "9957","periostitis","mondo","0004934"
> "9953","B- and T-cell mixed leukemia","icd10cm","C95.0"
> "9953","B- and T-cell mixed leukemia","mesh","D015456"
> "9953","B- and T-cell mixed leukemia","umls","C0023464"
> "9953","B- and T-cell mixed leukemia","mondo","0006667"
> "9952","acute lymphocytic leukemia","icd10cm","C91.0"
> "9952","acute lymphocytic leukemia","icd10cm","C91.00"
> "9952","acute lymphocytic leukemia","icd9cm","204.0"
> "9952","acute lymphocytic leukemia","umls","C0023449"
> "9952","acute lymphocytic leukemia","mondo","0004967"
> "201","connective tissue cancer","mesh","D009372"
> "201","connective tissue cancer","umls","C0027656"
> "201","connective tissue cancer","mondo","0002176"
> "0060871","autosomal dominant keratitis-ichthyosis-deafness syndrome","icd10cm","Q80.8"
> "0060871","autosomal dominant keratitis-ichthyosis-deafness syndrome","mondo","0007850"
> "0060872","isolated growth hormone deficiency type II","icd10cm","E23.0"
> "0060872","isolated growth hormone deficiency type II","mondo","0008250"
> "0060873","isolated growth hormone deficiency type IA","icd10cm","E23.0"
> "0060873","isolated growth hormone deficiency type IA","mondo","0009876"
> "0060874","isolated growth hormone deficiency type IB","icd10cm","E23.0"
> "0060874","isolated growth hormone deficiency type IB","mondo","0013006"
> "0060875","isolated growth hormone deficiency type III","icd10cm","E23.0"
> "0060875","isolated growth hormone deficiency type III","mondo","0010615"
> "0060877","bullous congenital ichthyosiform erythroderma","mesh","D053560"
> "0060877","bullous congenital ichthyosiform erythroderma","umls","C0432306"
> "0060877","bullous congenital ichthyosiform erythroderma","mondo","0007813"
> "0060878","hypoparathyroidism-deafness-renal disease syndrome","mesh","C537907"
> "0060878","hypoparathyroidism-deafness-renal disease syndrome","umls","C1840333"
> "0060878","hypoparathyroidism-deafness-renal disease syndrome","mondo","0007797"
> "0060879","primary hypomagnesemia","icd10cm","E83.4"
> "0060879","primary hypomagnesemia","mondo","0018100"
> "12043","kernicterus due to isoimmunization","icd10cm","P57.0"
> "12043","kernicterus due to isoimmunization","icd9cm","773.4"
> "12043","kernicterus due to isoimmunization","umls","C0270204"
> "12043","kernicterus due to isoimmunization","mondo","0006567"
> "350","mastocytosis","icd10cm","D47.09"
> "350","mastocytosis","icd10cm","D89.40"
> "350","mastocytosis","icd10cm","Q82.2"
> "350","mastocytosis","mesh","D008415"
> "350","mastocytosis","umls","C0024899"
> "350","mastocytosis","mondo","0007950"
> "8881","rosacea","icd10cm","L71"
> "8881","rosacea","icd10cm","L71.9"
> "8881","rosacea","icd9cm","695.3"
> "8881","rosacea","mesh","D012393"
> "8881","rosacea","umls","C0035854"
> "8881","rosacea","mondo","0006604"
> "3659","sialuria","mesh","D029461"
> "3659","sialuria","umls","C0342853"
> "3659","sialuria","mondo","0010028"
> "3650","lactic acidosis","icd10cm","E87.2"
> "3650","lactic acidosis","mesh","D000140"
> "3650","lactic acidosis","umls","C0001125"
> "3650","lactic acidosis","mondo","0024306"
> "3651","pyruvate carboxylase deficiency disease","icd10cm","E74.4"
> "3651","pyruvate carboxylase deficiency disease","mesh","D015324"
> "3651","pyruvate carboxylase deficiency disease","umls","C0034341"
> "3651","pyruvate carboxylase deficiency disease","mondo","0009949"
> "3652","Leigh disease","icd10cm","G31.82"
> "3652","Leigh disease","mesh","D007888"
> "3652","Leigh disease","umls","C0023264"
> "3652","Leigh disease","mondo","0018859"
> "2527","nephrosis","mesh","D009401"
> "2527","nephrosis","umls","C0027720"
> "2527","nephrosis","mondo","0002331"
> "2526","prostate adenocarcinoma","umls","C0007112"
> "2526","prostate adenocarcinoma","mondo","0005082"
> "0111170","autosomal dominant sensory ataxia 1","mondo","0012166"
> "2529","splenic disease","icd10cm","D73"
> "2529","splenic disease","icd10cm","D73.9"
> "2529","splenic disease","icd9cm","289.50"
> "2529","splenic disease","mesh","D013158"
> "2529","splenic disease","umls","C0037997"
> "2529","splenic disease","mondo","0002332"
> "0090058","torsion dystonia with onset in infancy","icd10cm","G24.1"
> "0090058","torsion dystonia with onset in infancy","mondo","0011249"
> "11465","autonomic nervous system disease","icd9cm","337.1"
> "11465","autonomic nervous system disease","umls","C0154691"
> "11465","autonomic nervous system disease","mondo","0001292"
> "0050662","bestrophinopathy","mesh","C567518"
> "0050662","bestrophinopathy","mondo","0012733"
> "0050663","Bethlem myopathy","mondo","0008029"
> "0050660","Beare-Stevenson cutis gyrata syndrome","mondo","0007412"
> "0050661","vitelliform macular dystrophy","icd10cm","H35.5"
> "0050661","vitelliform macular dystrophy","mesh","D057826"
> "0050661","vitelliform macular dystrophy","mondo","0000390"
> "0050664","Bietti crystalline corneoretinal dystrophy","mondo","0008865"
> "5062","phencyclidine abuse","mesh","D010623"
> "5062","phencyclidine abuse","umls","C0031391"
> "5062","phencyclidine abuse","mondo","0005912"
> "10787","premature menopause","icd10cm","E28.31"
> "10787","premature menopause","icd10cm","E28.319"
> "10787","premature menopause","icd9cm","256.31"
> "10787","premature menopause","mesh","D008594"
> "10787","premature menopause","umls","C0025322"
> "10787","premature menopause","mondo","0001119"
> "0111350","Laurin-Sandrow syndrome","mesh","C535689"
> "0111350","Laurin-Sandrow syndrome","umls","C1851100"
> "4409","folliculitis","mesh","D005499"
> "4409","folliculitis","umls","C0016436"
> "4409","folliculitis","mondo","0006552"
> "4404","occupational dermatitis","mesh","D009783"
> "4404","occupational dermatitis","umls","C0028796"
> "4404","occupational dermatitis","mondo","0006589"
> "4406","spongiotic dermatitis","umls","C0262984"
> "4406","spongiotic dermatitis","mondo","0002987"
> "4407","phototoxic dermatitis","mesh","D017484"
> "4407","phototoxic dermatitis","umls","C0162830"
> "4407","phototoxic dermatitis","mondo","0006598"
> "4400","dermatosis papulosa nigra","icd10cm","L82"
> "4400","dermatosis papulosa nigra","mesh","C562379"
> "4400","dermatosis papulosa nigra","umls","C0011645"
> "4400","dermatosis papulosa nigra","mondo","0007446"
> "13310","diphtheritic peritonitis","icd10cm","A36.89"
> "13310","diphtheritic peritonitis","icd9cm","032.83"
> "13310","diphtheritic peritonitis","umls","C0152953"
> "13310","diphtheritic peritonitis","mondo","0001682"
> "13313","pancreatic mucinous ductal ectasia","umls","C1335310"
> "13313","pancreatic mucinous ductal ectasia","mondo","0001683"
> "929","myopathy of extraocular muscle","icd10cm","H05.82"
> "929","myopathy of extraocular muscle","icd9cm","376.82"
> "929","myopathy of extraocular muscle","umls","C0155286"
> "929","myopathy of extraocular muscle","mondo","0004746"
> "9577","neonatal candidiasis","icd10cm","P37.5"
> "9577","neonatal candidiasis","icd9cm","771.7"
> "9577","neonatal candidiasis","umls","C0276682"
> "9577","neonatal candidiasis","mondo","0004824"
> "9574","choanal atresia","icd10cm","Q30.0"
> "9574","choanal atresia","icd9cm","748.0"
> "9574","choanal atresia","mesh","C562435"
> "9574","choanal atresia","mesh","D002754"
> "9574","choanal atresia","umls","C0008297"
> "9574","choanal atresia","umls","C0220723"
> "9574","choanal atresia","mondo","0012155"
> "10754","otitis media","icd10cm","H66.9"
> "10754","otitis media","icd10cm","H66.90"
> "10754","otitis media","icd9cm","382.9"
> "10754","otitis media","mesh","D010033"
> "10754","otitis media","umls","C0029882"
> "10754","otitis media","mondo","0005441"
> "10755","petrositis","icd10cm","H70.2"
> "10755","petrositis","icd10cm","H70.20"
> "10755","petrositis","icd10cm","H70.209"
> "10755","petrositis","icd10cm","H70.21"
> "10755","petrositis","icd10cm","H70.219"
> "10755","petrositis","icd10cm","H70.22"
> "10755","petrositis","icd10cm","H70.229"
> "10755","petrositis","icd9cm","383.2"
> "10755","petrositis","icd9cm","383.20"
> "10755","petrositis","icd9cm","383.21"
> "10755","petrositis","icd9cm","383.22"
> "10755","petrositis","mesh","D059270"
> "10755","petrositis","umls","C0155448"
> "10755","petrositis","umls","C0155449"
> "10755","petrositis","umls","C0155450"
> "10755","petrositis","mondo","0001109"
> "5393","brain angioma","umls","C0238814"
> "5393","brain angioma","mondo","0003428"
> "5392","acidophil adenoma","mesh","D000239"
> "5392","acidophil adenoma","umls","C0001433"
> "5392","acidophil adenoma","mondo","0006634"
> "5391","bronchus adenoma","umls","C0149845"
> "5391","bronchus adenoma","mondo","0003427"
> "5390","clear cell adenoma","umls","C0334315"
> "5390","clear cell adenoma","mondo","0003426"
> "5396","prolactin producing pituitary tumor","umls","C0278863"
> "5396","prolactin producing pituitary tumor","umls","C1334614"
> "5396","prolactin producing pituitary tumor","mondo","0003430"
> "5395","functioning pituitary adenoma","umls","C0854486"
> "5395","functioning pituitary adenoma","mondo","0003429"
> "5394","prolactinoma","mesh","D015175"
> "5394","prolactinoma","umls","C0033375"
> "5394","prolactinoma","mondo","0010911"
> "11801","protein-energy malnutrition","icd10cm","E46"
> "11801","protein-energy malnutrition","icd9cm","263.9"
> "11801","protein-energy malnutrition","mesh","D011502"
> "11801","protein-energy malnutrition","umls","C0033677"
> "11801","protein-energy malnutrition","mondo","0001371"
> "5398","lipoadenoma","umls","C0334325"
> "5398","lipoadenoma","mondo","0003431"
> "0111433","optic atrophy 3","mesh","C537128"
> "0111433","optic atrophy 3","umls","C1833809"
> "6590","spondylitis","icd10cm","M46"
> "6590","spondylitis","icd9cm","720.8"
> "6590","spondylitis","icd9cm","720.89"
> "6590","spondylitis","mesh","D013166"
> "6590","spondylitis","umls","C0029644"
> "6590","spondylitis","mondo","0003937"
> "784","chronic kidney disease","icd10cm","N18.9"
> "784","chronic kidney disease","icd9cm","585.6"
> "784","chronic kidney disease","mesh","D007676"
> "784","chronic kidney disease","umls","C0022661"
> "784","chronic kidney disease","mondo","0005300"
> "9396","acute laryngitis","icd10cm","J04.0"
> "9396","acute laryngitis","icd9cm","464.0"
> "9396","acute laryngitis","icd9cm","464.01"
> "9396","acute laryngitis","umls","C0001327"
> "9396","acute laryngitis","umls","C0949123"
> "9396","acute laryngitis","mondo","0004777"
> "786","laryngeal disease","icd10cm","J38.7"
> "786","laryngeal disease","icd10cm","S12.8"
> "786","laryngeal disease","icd9cm","478.70"
> "786","laryngeal disease","mesh","D007818"
> "786","laryngeal disease","umls","C0023051"
> "786","laryngeal disease","mondo","0004382"
> "780","placenta disease","icd10cm","O43"
> "780","placenta disease","icd10cm","O43.9"
> "780","placenta disease","icd10cm","O43.90"
> "780","placenta disease","icd9cm","646.9"
> "780","placenta disease","mesh","D010922"
> "780","placenta disease","mesh","D011248"
> "780","placenta disease","umls","C0032045"
> "780","placenta disease","umls","C0032962"
> "780","placenta disease","umls","C0151864"
> "780","placenta disease","umls","C1335423"
> "780","placenta disease","mondo","0005917"
> "9392","tracheitis","icd10cm","J04.1"
> "9392","tracheitis","icd9cm","464.1"
> "9392","tracheitis","mesh","D014136"
> "9392","tracheitis","umls","C0040584"
> "9392","tracheitis","umls","C0149513"
> "9392","tracheitis","mondo","0005990"
> "782","renal infectious disease","icd10cm","N15.9"
> "782","renal infectious disease","icd9cm","590"
> "782","renal infectious disease","icd9cm","590.9"
> "782","renal infectious disease","umls","C0021313"
> "782","renal infectious disease","mondo","0004369"
> "9398","epiglottitis","icd10cm","J05.1"
> "9398","epiglottitis","icd10cm","J05.10"
> "9398","epiglottitis","icd9cm","464.3"
> "9398","epiglottitis","mesh","D004826"
> "9398","epiglottitis","umls","C0014541"
> "9398","epiglottitis","umls","C0155814"
> "9398","epiglottitis","mondo","0005753"
> "0110401","retinitis pigmentosa 74","icd10cm","H35.5"
> "0110401","retinitis pigmentosa 74","mondo","0014692"
> "0110400","retinitis pigmentosa 22","icd10cm","H35.5"
> "0110400","retinitis pigmentosa 22","mondo","0011259"
> "0110403","retinitis pigmentosa 13","icd10cm","H35.5"
> "0110403","retinitis pigmentosa 13","mondo","0010806"
> "0110402","retinitis pigmentosa 45","icd10cm","H35.5"
> "0110402","retinitis pigmentosa 45","mondo","0013413"
> "0110405","retinitis pigmentosa 36","icd10cm","H35.5"
> "0110405","retinitis pigmentosa 36","mondo","0012523"
> "0110404","retinitis pigmentosa 17","icd10cm","H35.5"
> "0110404","retinitis pigmentosa 17","mondo","0010945"
> "0110407","retinitis pigmentosa 57","icd10cm","H35.5"
> "0110407","retinitis pigmentosa 57","mondo","0013315"
> "0110406","retinitis pigmentosa 30","icd10cm","H35.5"
> "0110406","retinitis pigmentosa 30","mondo","0011935"
> "0110409","retinitis pigmentosa 46","icd10cm","H35.5"
> "0110409","retinitis pigmentosa 46","mondo","0012943"
> "0110408","retinitis pigmentosa 11","icd10cm","H35.5"
> "0110408","retinitis pigmentosa 11","mondo","0010828"
> "252","alcoholic psychosis","icd9cm","291.9"
> "252","alcoholic psychosis","mesh","D011604"
> "252","alcoholic psychosis","umls","C0033936"
> "252","alcoholic psychosis","mondo","0002330"
> "0060203","amyotrophic lateral sclerosis type 12","mondo","0013264"
> "0060202","amyotrophic lateral sclerosis type 11","mondo","0012945"
> "0060201","amyotrophic lateral sclerosis type 10","mondo","0012790"
> "0060200","amyotrophic lateral sclerosis type 9","mondo","0012753"
> "0060207","amyotrophic lateral sclerosis type 16","mondo","0013715"
> "0060206","amyotrophic lateral sclerosis type 15","mondo","0010459"
> "0060205","amyotrophic lateral sclerosis type 14","mondo","0013501"
> "0060209","amyotrophic lateral sclerosis type 18","mondo","0013891"
> "0060208","amyotrophic lateral sclerosis type 17","mondo","0013861"
> "7152","prostate stromal sarcoma","umls","C1335521"
> "7152","prostate stromal sarcoma","mondo","0004124"
> "1375","neonatal urinary tract infectious disease","icd10cm","P39.3"
> "1375","neonatal urinary tract infectious disease","icd9cm","771.82"
> "1375","neonatal urinary tract infectious disease","umls","C0235815"
> "1375","neonatal urinary tract infectious disease","mondo","0001791"
> "8068","intraductal breast myoepitheliosis","umls","C1512935"
> "8068","intraductal breast myoepitheliosis","mondo","0004449"
> "9395","croup","icd10cm","J05.0"
> "9395","croup","icd9cm","464.4"
> "9395","croup","mesh","D003440"
> "9395","croup","umls","C0010380"
> "9395","croup","mondo","0005722"
> "8060","frontal sinus inverted papilloma","umls","C1333644"
> "8060","frontal sinus inverted papilloma","mondo","0004448"
> "7480","large cell carcinoma with rhabdoid phenotype","umls","C1265997"
> "7480","large cell carcinoma with rhabdoid phenotype","mondo","0004237"
> "7483","cervical keratinizing squamous cell carcinoma","umls","C1517658"
> "7483","cervical keratinizing squamous cell carcinoma","mondo","0004239"
> "7482","petrous apex meningioma","umls","C1335396"
> "7482","petrous apex meningioma","mondo","0004238"
> "251","alcohol-induced mental disorder","icd9cm","291.8"
> "251","alcohol-induced mental disorder","icd9cm","291.89"
> "251","alcohol-induced mental disorder","umls","C1456283"
> "251","alcohol-induced mental disorder","mondo","0002326"
> "7489","Osgood-Schlatter's disease","mesh","D055034"
> "7489","Osgood-Schlatter's disease","umls","C0029376"
> "7489","Osgood-Schlatter's disease","mondo","0004241"
> "7488","posterior urethra cancer","umls","C0279931"
> "7488","posterior urethra cancer","mondo","0004240"
> "13593","eclampsia","icd10cm","O15"
> "13593","eclampsia","icd10cm","O15.9"
> "13593","eclampsia","mesh","D004461"
> "13593","eclampsia","umls","C0013537"
> "13593","eclampsia","mondo","0001754"
> "2891","thyroid adenoma","mesh","D013964"
> "2891","thyroid adenoma","umls","C0151468"
> "2891","thyroid adenoma","mondo","0002454"
> "2893","cervix carcinoma","umls","C0302592"
> "2893","cervix carcinoma","mondo","0005131"
> "2892","exocervical carcinoma","umls","C1299238"
> "2892","exocervical carcinoma","mondo","0002455"
> "1106","esophagus lymphoma","umls","C1333459"
> "1106","esophagus lymphoma","mondo","0001188"
> "1107","esophageal carcinoma","umls","C0152018"
> "1107","esophageal carcinoma","mondo","0019086"
> "0050989","episodic ataxia type 1","mondo","0008047"
> "1100","ovarian disease","mesh","D010049"
> "1100","ovarian disease","umls","C0029928"
> "1100","ovarian disease","mondo","0005558"
> "1453","atrophic glossitis","icd10cm","K14.4"
> "1453","atrophic glossitis","icd9cm","529.4"
> "1453","atrophic glossitis","umls","C0155964"
> "1453","atrophic glossitis","mondo","0001989"
> "0050983","spinocerebellar ataxia type 36","mondo","0013594"
> "0050982","spinocerebellar ataxia type 35","mondo","0013485"
> "0050981","spinocerebellar ataxia type 34","mondo","0007574"
> "0050980","spinocerebellar ataxia type 31","mondo","0007296"
> "1458","postsurgical hypothyroidism","icd10cm","E89.0"
> "1458","postsurgical hypothyroidism","icd9cm","244.0"
> "1458","postsurgical hypothyroidism","umls","C0154157"
> "1458","postsurgical hypothyroidism","mondo","0002002"
> "1459","hypothyroidism","icd10cm","E03.9"
> "1459","hypothyroidism","icd9cm","244.9"
> "1459","hypothyroidism","mesh","D007037"
> "1459","hypothyroidism","umls","C0020676"
> "1459","hypothyroidism","mondo","0005420"
> "0050985","spinocerebellar ataxia type 38","mondo","0014417"
> "0050984","spinocerebellar ataxia type 37","mondo","0014410"
> "3737","verrucous carcinoma","mesh","D018289"
> "3737","verrucous carcinoma","umls","C0206706"
> "3737","verrucous carcinoma","mondo","0006006"
> "1895","allergic contact dermatitis of eyelid","icd9cm","373.32"
> "1895","allergic contact dermatitis of eyelid","umls","C0155178"
> "1895","allergic contact dermatitis of eyelid","mondo","0002138"
> "254","hemangioma of intra-abdominal structure","icd10cm","D18.03"
> "254","hemangioma of intra-abdominal structure","icd9cm","228.04"
> "254","hemangioma of intra-abdominal structure","umls","C0154052"
> "254","hemangioma of intra-abdominal structure","mondo","0002337"
> "4691","malignant mediastinal neurogenic neoplasm","umls","C1334672"
> "4691","malignant mediastinal neurogenic neoplasm","mondo","0003098"
> "4690","childhood mediastinal neurogenic tumor","umls","C1332981"
> "4690","childhood mediastinal neurogenic tumor","mondo","0003097"
> "4693","nerve plexus neoplasm","umls","C1334945"
> "4693","nerve plexus neoplasm","mondo","0003100"
> "4692","endophthalmitis","mesh","D009877"
> "4692","endophthalmitis","umls","C0014236"
> "4692","endophthalmitis","mondo","0016047"
> "4798","aggressive systemic mastocytosis","icd10cm","C96.21"
> "4798","aggressive systemic mastocytosis","mesh","D034721"
> "4798","aggressive systemic mastocytosis","umls","C1112486"
> "4798","aggressive systemic mastocytosis","mondo","0020333"
> "4794","ependymoblastoma","mesh","D018242"
> "4794","ependymoblastoma","umls","C0700367"
> "4794","ependymoblastoma","mondo","0016715"
> "4795","GM2 gangliosidosis, AB variant","mesh","D049290"
> "4795","GM2 gangliosidosis, AB variant","umls","C0268275"
> "4795","GM2 gangliosidosis, AB variant","mondo","0010099"
> "4796","space motion sickness","mesh","D018489"
> "4796","space motion sickness","umls","C0242700"
> "4796","space motion sickness","mondo","0003147"
> "4797","SM-AHNMD","umls","C1301365"
> "4797","SM-AHNMD","mondo","0003148"
> "4790","medulloepithelioma","mesh","D018242"
> "4790","medulloepithelioma","umls","C0334596"
> "4790","medulloepithelioma","mondo","0003144"
> "4791","supratentorial primitive neuroectodermal tumor","umls","C1336538"
> "4791","supratentorial primitive neuroectodermal tumor","mondo","0003145"
> "2133","central nervous system sarcoma","umls","C1332892"
> "2133","central nervous system sarcoma","mondo","0002217"
> "5834","spermatocytoma","umls","C0334517"
> "5834","spermatocytoma","mondo","0020513"
> "5830","cervical endometrioid adenocarcinoma","umls","C1332913"
> "5830","cervical endometrioid adenocarcinoma","mondo","0003665"
> "5831","fallopian tube endometrioid adenocarcinoma","umls","C1333592"
> "5831","fallopian tube endometrioid adenocarcinoma","umls","C1517113"
> "5831","fallopian tube endometrioid adenocarcinoma","mondo","0003666"
> "11256","typhus","icd10cm","A75"
> "11256","typhus","icd10cm","A75.0"
> "11256","typhus","icd10cm","A75.2"
> "11256","typhus","icd10cm","A75.9"
> "11256","typhus","icd9cm","080"
> "11256","typhus","icd9cm","081.0"
> "11256","typhus","icd9cm","081.9"
> "11256","typhus","mesh","D014437"
> "11256","typhus","mesh","D014438"
> "11256","typhus","umls","C0041471"
> "11256","typhus","umls","C0041472"
> "11256","typhus","umls","C0041473"
> "11256","typhus","mondo","0001246"
> "11257","social phobia","icd10cm","F40.1"
> "11257","social phobia","icd10cm","F40.10"
> "11257","social phobia","icd9cm","300.23"
> "11257","social phobia","mesh","D000072861"
> "11257","social phobia","umls","C0031572"
> "11257","social phobia","mondo","0001247"
> "11254","Brill-Zinsser disease","icd10cm","A75.1"
> "11254","Brill-Zinsser disease","icd9cm","081.1"
> "11254","Brill-Zinsser disease","mesh","D014438"
> "11254","Brill-Zinsser disease","umls","C0006181"
> "11254","Brill-Zinsser disease","mondo","0005680"
> "11252","microcytic anemia","mesh","C562385"
> "11252","microcytic anemia","umls","C0085576"
> "11252","microcytic anemia","mondo","0001245"
> "13722","neuroschistosomiasis","mesh","D020818"
> "13722","neuroschistosomiasis","umls","C0752191"
> "13722","neuroschistosomiasis","mondo","0005874"
> "5838","extragonadal seminoma","umls","C1333502"
> "5838","extragonadal seminoma","mondo","0003668"
> "0110874","holoprosencephaly 6","mondo","0011616"
> "0110875","holoprosencephaly 3","mondo","0007733"
> "13724","scurvy","icd10cm","E54"
> "13724","scurvy","mesh","D012614"
> "13724","scurvy","umls","C0036474"
> "13724","scurvy","mondo","0009412"
> "0110876","holoprosencephaly 7","mondo","0012562"
> "13725","beriberi","icd10cm","E51.1"
> "13725","beriberi","icd9cm","265.0"
> "13725","beriberi","mesh","D001602"
> "13725","beriberi","umls","C0005122"
> "13725","beriberi","mondo","0006676"
> "0110877","holoprosencephaly 11","mondo","0013642"
> "0110870","congenital stationary night blindness 1A","mondo","0010690"
> "0110871","congenital stationary night blindness 2A","mondo","0010241"
> "11786","splenic sequestration","icd9cm","289.52"
> "11786","splenic sequestration","umls","C1260402"
> "11786","splenic sequestration","mondo","0001366"
> "11787","chronic congestive splenomegaly","icd10cm","D73.2"
> "11787","chronic congestive splenomegaly","icd9cm","289.51"
> "11787","chronic congestive splenomegaly","umls","C0398661"
> "11787","chronic congestive splenomegaly","mondo","0001367"
> "0110872","holoprosencephaly 2","mondo","0007999"
> "11782","astigmatism","icd10cm","H52.2"
> "11782","astigmatism","icd10cm","H52.20"
> "11782","astigmatism","icd9cm","367.2"
> "11782","astigmatism","icd9cm","367.20"
> "11782","astigmatism","mesh","D001251"
> "11782","astigmatism","umls","C0004106"
> "11782","astigmatism","mondo","0011284"
> "11783","necrosis of ear ossicle","icd9cm","385.24"
> "11783","necrosis of ear ossicle","umls","C0155488"
> "11783","necrosis of ear ossicle","mondo","0001365"
> "0110873","holoprosencephaly 9","mondo","0012563"
> "4","disease","mesh","D004194"
> "4","disease","umls","C0012634"
> "4","disease","mondo","0000001"
> "12782","cicatricial ectropion","icd9cm","374.14"
> "12782","cicatricial ectropion","umls","C0155196"
> "12782","cicatricial ectropion","mondo","0001582"
> "12785","diabetic polyneuropathy","icd9cm","357.2"
> "12785","diabetic polyneuropathy","mesh","D003929"
> "12785","diabetic polyneuropathy","umls","C0271680"
> "12785","diabetic polyneuropathy","mondo","0001583"
> "10321","baritosis","mesh","C537080"
> "10321","baritosis","umls","C0340177"
> "10321","baritosis","mondo","0001001"
> "10320","asbestosis","icd10cm","J61"
> "10320","asbestosis","icd9cm","501"
> "10320","asbestosis","mesh","D001195"
> "10320","asbestosis","umls","C0003949"
> "10320","asbestosis","mondo","0016466"
> "10323","byssinosis","icd10cm","J66.0"
> "10323","byssinosis","mesh","D002095"
> "10323","byssinosis","umls","C0006542"
> "10323","byssinosis","mondo","0006688"
> "10322","berylliosis","icd10cm","J63.2"
> "10322","berylliosis","mesh","D001607"
> "10322","berylliosis","umls","C0005138"
> "10322","berylliosis","mondo","0015274"
> "10325","silicosis","icd10cm","J62"
> "10325","silicosis","icd10cm","J62.8"
> "10325","silicosis","icd9cm","502"
> "10325","silicosis","mesh","D012829"
> "10325","silicosis","umls","C0037116"
> "10325","silicosis","mondo","0005960"
> "10324","anthracosilicosis","icd10cm","J60"
> "10324","anthracosilicosis","mesh","D000874"
> "10324","anthracosilicosis","umls","C0003164"
> "10324","anthracosilicosis","mondo","0006653"
> "10327","anthracosis","icd10cm","J60"
> "10327","anthracosis","icd9cm","500"
> "10327","anthracosis","mesh","D055008"
> "10327","anthracosis","umls","C0003165"
> "10327","anthracosis","mondo","0006654"
> "10070","larynx leiomyoma","umls","C1334370"
> "10070","larynx leiomyoma","mondo","0000934"
> "2770","obsolete diaper rash","icd10cm","L22"
> "2770","obsolete diaper rash","icd9cm","691.0"
> "2770","obsolete diaper rash","mesh","D003963"
> "2770","obsolete diaper rash","umls","C0011974"
> "4892","middle ear adenocarcinoma","umls","C1334758"
> "4892","middle ear adenocarcinoma","mondo","0003189"
> "2772","irritant dermatitis","icd10cm","L24"
> "2772","irritant dermatitis","icd10cm","L24.9"
> "2772","irritant dermatitis","mesh","D017453"
> "2772","irritant dermatitis","umls","C0162823"
> "2772","irritant dermatitis","mondo","0006564"
> "2773","contact dermatitis","icd10cm","L25"
> "2773","contact dermatitis","icd10cm","L25.9"
> "2773","contact dermatitis","mesh","D003877"
> "2773","contact dermatitis","umls","C0011616"
> "2773","contact dermatitis","mondo","0005480"
> "4897","bile duct carcinoma","mesh","D001650"
> "4897","bile duct carcinoma","umls","C0740277"
> "4897","bile duct carcinoma","mondo","0005496"
> "2775","long bone adamantinoma","mesh","C562741"
> "2775","long bone adamantinoma","umls","C0334556"
> "2775","long bone adamantinoma","mondo","0002422"
> "2776","adamantinoma","mesh","D050398"
> "2776","adamantinoma","umls","C1367554"
> "2776","adamantinoma","mondo","0002422"
> "4894","rete ovarii adenocarcinoma","umls","C3840223"
> "4894","rete ovarii adenocarcinoma","mondo","0003191"
> "9498","pulmonary eosinophilia","icd9cm","518.3"
> "9498","pulmonary eosinophilia","mesh","D011657"
> "9498","pulmonary eosinophilia","umls","C0034068"
> "9498","pulmonary eosinophilia","mondo","0004802"
> "9499","disseminated eosinophilic collagen disease","umls","C0263662"
> "9499","disseminated eosinophilic collagen disease","mondo","0004803"
> "9149","hard palate cancer","icd10cm","C05.0"
> "9149","hard palate cancer","icd9cm","145.2"
> "9149","hard palate cancer","umls","C0153375"
> "9149","hard palate cancer","mondo","0004719"
> "0070100","oculocutaneous albinism type VII","mondo","0014070"
> "9140","xeroderma of eyelid","icd10cm","H01.14"
> "9140","xeroderma of eyelid","icd9cm","373.33"
> "9140","xeroderma of eyelid","umls","C0155179"
> "9140","xeroderma of eyelid","mondo","0004718"
> "7971","microcystic variant infiltrating bladder urothelial carcinoma","umls","C1512740"
> "7971","microcystic variant infiltrating bladder urothelial carcinoma","mondo","0004418"
> "9496","unilateral hypoactive labyrinth","icd9cm","386.53"
> "9496","unilateral hypoactive labyrinth","umls","C0155517"
> "9496","unilateral hypoactive labyrinth","mondo","0004801"
> "7972","lymphoma-like variant infiltrating bladder urothelial carcinoma","umls","C1512739"
> "7972","lymphoma-like variant infiltrating bladder urothelial carcinoma","mondo","0004419"
> "12257","medulloadrenal hyperfunction","icd10cm","E27.5"
> "12257","medulloadrenal hyperfunction","icd9cm","255.6"
> "12257","medulloadrenal hyperfunction","umls","C0154206"
> "12257","medulloadrenal hyperfunction","mondo","0001473"
> "7522","pediatric infratentorial ependymoblastoma","umls","C1332972"
> "7522","pediatric infratentorial ependymoblastoma","mondo","0004263"
> "2034","encephalomalacia","mesh","D004678"
> "2034","encephalomalacia","umls","C0014068"
> "2034","encephalomalacia","mondo","0006741"
> "6262","follicular dendritic cell sarcoma","icd10cm","C96.4"
> "6262","follicular dendritic cell sarcoma","mesh","D054740"
> "6262","follicular dendritic cell sarcoma","umls","C1260325"
> "6262","follicular dendritic cell sarcoma","mondo","0005764"
> "6263","inflammatory breast carcinoma","mesh","D058922"
> "6263","inflammatory breast carcinoma","umls","C0278601"
> "6263","inflammatory breast carcinoma","mondo","0006804"
> "12259","hemophilia B","icd10cm","D67"
> "12259","hemophilia B","icd9cm","286.1"
> "12259","hemophilia B","mesh","D002836"
> "12259","hemophilia B","umls","C0008533"
> "12259","hemophilia B","mondo","0010604"
> "10079","cysticercosis","icd10cm","B69"
> "10079","cysticercosis","icd10cm","B69.9"
> "10079","cysticercosis","icd9cm","123.1"
> "10079","cysticercosis","mesh","D003551"
> "10079","cysticercosis","umls","C0010678"
> "10079","cysticercosis","mondo","0015484"
> "9726","vitreous detachment","icd10cm","H43.81"
> "9726","vitreous detachment","mesh","D020255"
> "9726","vitreous detachment","umls","C0042907"
> "9726","vitreous detachment","mondo","0007017"
> "9724","purulent endophthalmitis","icd10cm","H44.0"
> "9724","purulent endophthalmitis","icd10cm","H44.00"
> "9724","purulent endophthalmitis","icd9cm","360.0"
> "9724","purulent endophthalmitis","icd9cm","360.00"
> "9724","purulent endophthalmitis","umls","C0259800"
> "9724","purulent endophthalmitis","mondo","0004863"
> "9722","ophthalmia nodosa","icd10cm","H16.24"
> "9722","ophthalmia nodosa","icd9cm","360.14"
> "9722","ophthalmia nodosa","umls","C0154775"
> "9722","ophthalmia nodosa","mondo","0004861"
> "9723","vitreous abscess","icd9cm","360.04"
> "9723","vitreous abscess","umls","C0042904"
> "9723","vitreous abscess","mondo","0004862"
> "9720","vitreous disease","icd10cm","H43.3"
> "9720","vitreous disease","icd10cm","H43.39"
> "9720","vitreous disease","icd9cm","379.24"
> "9720","vitreous disease","umls","C0029872"
> "9720","vitreous disease","mondo","0004860"
> "0111474","combined oxidative phosphorylation deficiency 1","umls","C1836797"
> "845","cyclothymic disorder","icd10cm","F34.0"
> "845","cyclothymic disorder","icd9cm","301.1"
> "845","cyclothymic disorder","icd9cm","301.10"
> "845","cyclothymic disorder","icd9cm","301.13"
> "845","cyclothymic disorder","mesh","D003527"
> "845","cyclothymic disorder","umls","C0010598"
> "845","cyclothymic disorder","mondo","0004572"
> "3463","breast disease","icd10cm","N60-N65"
> "3463","breast disease","icd10cm","N64.9"
> "3463","breast disease","icd9cm","610-612.99"
> "3463","breast disease","icd9cm","611.9"
> "3463","breast disease","mesh","D001941"
> "3463","breast disease","umls","C0006145"
> "3463","breast disease","mondo","0002657"
> "841","extrinsic allergic alveolitis","icd10cm","J67.9"
> "841","extrinsic allergic alveolitis","icd9cm","495"
> "841","extrinsic allergic alveolitis","icd9cm","495.9"
> "841","extrinsic allergic alveolitis","mesh","D000542"
> "841","extrinsic allergic alveolitis","umls","C0002390"
> "841","extrinsic allergic alveolitis","mondo","0004553"
> "840","cork-handlers' disease","icd10cm","J67.3"
> "840","cork-handlers' disease","icd9cm","495.3"
> "840","cork-handlers' disease","umls","C0152108"
> "840","cork-handlers' disease","mondo","0004549"
> "8893","psoriasis","icd10cm","L40"
> "8893","psoriasis","icd10cm","L40.9"
> "8893","psoriasis","mesh","D011565"
> "8893","psoriasis","umls","C0033860"
> "8893","psoriasis","mondo","0005083"
> "8892","pityriasis rosea","icd10cm","L42"
> "8892","pityriasis rosea","icd9cm","696.3"
> "8892","pityriasis rosea","mesh","D017515"
> "8892","pityriasis rosea","umls","C0032026"
> "8892","pityriasis rosea","mondo","0006601"
> "849","rheumatoid arthritis interstitial lung disease","icd9cm","714.81"
> "849","rheumatoid arthritis interstitial lung disease","mondo","0004586"
> "848","arthritis","icd10cm","M19.90"
> "848","arthritis","mesh","D001168"
> "848","arthritis","umls","C0003864"
> "848","arthritis","mondo","0005578"
> "13794","anterior scleritis","icd10cm","H15.01"
> "13794","anterior scleritis","icd9cm","379.03"
> "13794","anterior scleritis","umls","C0155353"
> "13794","anterior scleritis","mondo","0001804"
> "5238","benign perivascular tumor","umls","C1332532"
> "5238","benign perivascular tumor","mondo","0003342"
> "1738","small intestine leiomyoma","umls","C0238197"
> "1738","small intestine leiomyoma","mondo","0002092"
> "5230","hepatoerythropoietic porphyria","mesh","D017121"
> "5230","hepatoerythropoietic porphyria","umls","C0162569"
> "5230","hepatoerythropoietic porphyria","mondo","0019799"
> "5232","aortic valve prolapse","mesh","D001023"
> "5232","aortic valve prolapse","umls","C0003505"
> "5232","aortic valve prolapse","mondo","0006655"
> "5233","glomangiosarcoma","umls","C1266111"
> "5233","glomangiosarcoma","mondo","0003340"
> "5236","subungual glomus tumor","umls","C1304510"
> "5236","subungual glomus tumor","mondo","0003341"
> "13127","gonococcal spondylitis","icd9cm","098.53"
> "13127","gonococcal spondylitis","umls","C0153219"
> "13127","gonococcal spondylitis","mondo","0001640"
> "13120","protein-deficiency anemia","icd10cm","D53.0"
> "13120","protein-deficiency anemia","icd9cm","281.4"
> "13120","protein-deficiency anemia","umls","C0154290"
> "13120","protein-deficiency anemia","mondo","0001638"
> "13121","deficiency anemia","icd9cm","281.9"
> "13121","deficiency anemia","umls","C0041782"
> "13121","deficiency anemia","mondo","0001639"
> "11718","antidepressant type abuse","icd9cm","305.8"
> "11718","antidepressant type abuse","umls","C0154540"
> "11718","antidepressant type abuse","mondo","0001345"
> "3070","malignant glioma","kegg","05214"
> "3070","malignant glioma","mesh","D005910"
> "3070","malignant glioma","umls","C0017638"
> "3070","malignant glioma","umls","C0555198"
> "3070","malignant glioma","mondo","0015917"
> "3071","gliosarcoma","mesh","D018316"
> "3071","gliosarcoma","umls","C0206726"
> "3071","gliosarcoma","mondo","0016681"
> "1596","mental depression","icd10cm","F32.9"
> "1596","mental depression","icd10cm","F33.9"
> "1596","mental depression","mesh","D003863"
> "1596","mental depression","umls","C0011570"
> "1596","mental depression","mondo","0002050"
> "3074","giant cell glioblastoma","mesh","D005909"
> "3074","giant cell glioblastoma","umls","C0334588"
> "3074","giant cell glioblastoma","mondo","0016682"
> "14319","pleuropneumonia","mesh","D011001"
> "14319","pleuropneumonia","umls","C0032241"
> "14319","pleuropneumonia","mondo","0001940"
> "3076","adult astrocytic tumour","umls","C1332183"
> "3076","adult astrocytic tumour","mondo","0002503"
> "3078","grade III astrocytoma","mesh","D001254"
> "3078","grade III astrocytoma","umls","C0334579"
> "3078","grade III astrocytoma","mondo","0016684"
> "3079","juvenile astrocytoma","umls","C1321865"
> "3079","juvenile astrocytoma","mondo","0002505"
> "0060438","Cole-Carpenter syndrome","mesh","C535963"
> "0060438","Cole-Carpenter syndrome","umls","C1862178"
> "0060438","Cole-Carpenter syndrome","mondo","0016085"
> "0060439","lysinuric protein intolerance","mesh","C562687"
> "0060439","lysinuric protein intolerance","umls","C0268647"
> "0060439","lysinuric protein intolerance","mondo","0009109"
> "10331","kaolin pneumoconiosis","umls","C0264435"
> "10331","kaolin pneumoconiosis","mondo","0001005"
> "0060430","chromosome 16p11.2 duplication syndrome","icd10cm","Q92.3"
> "0060430","chromosome 16p11.2 duplication syndrome","mondo","0013847"
> "0060431","chromosome 16p13.3 duplication syndrome","icd10cm","Q92.3"
> "0060431","chromosome 16p13.3 duplication syndrome","mondo","0013273"
> "0060432","chromosome 17p13.3 duplication syndrome","icd10cm","Q92.3"
> "0060432","chromosome 17p13.3 duplication syndrome","mondo","0013182"
> "0060433","chromosome 17q12 duplication syndrome","icd10cm","Q92.3"
> "0060433","chromosome 17q12 duplication syndrome","mondo","0013796"
> "0060434","chromosome 17q21.31 duplication syndrome","icd10cm","Q92.3"
> "0060434","chromosome 17q21.31 duplication syndrome","mondo","0013298"
> "0060435","chromosome 1q21.1 duplication syndrome","icd10cm","Q92.3"
> "0060435","chromosome 1q21.1 duplication syndrome","mondo","0012915"
> "0060436","chromosome 22q11.2 microduplication syndrome","icd10cm","Q92.3"
> "0060436","chromosome 22q11.2 microduplication syndrome","mesh","C567224"
> "0060436","chromosome 22q11.2 microduplication syndrome","mondo","0012020"
> "0060437","chromosome 22q13 duplication syndrome","mondo","0014235"
> "5648","choroid plexus carcinoma","mesh","C562943"
> "5648","choroid plexus carcinoma","umls","C0346289"
> "5648","choroid plexus carcinoma","umls","C0431109"
> "5648","choroid plexus carcinoma","mondo","0016718"
> "5641","diffuse pulmonary fibrosis","umls","C0865849"
> "5641","diffuse pulmonary fibrosis","mondo","0003563"
> "5643","urethral villous adenoma","umls","C1519828"
> "5643","urethral villous adenoma","mondo","0003565"
> "5642","localized pulmonary fibrosis","umls","C0340127"
> "5642","localized pulmonary fibrosis","mondo","0003564"
> "5644","tricuspid valve prolapse","mesh","D014263"
> "5644","tricuspid valve prolapse","umls","C0040962"
> "5644","tricuspid valve prolapse","mondo","0007001"
> "0111162","epidermal nevus","mondo","0008093"
> "2401","clitoris cancer","icd10cm","C51.2"
> "2401","clitoris cancer","icd9cm","184.3"
> "2401","clitoris cancer","umls","C0153589"
> "2401","clitoris cancer","umls","C1333070"
> "2401","clitoris cancer","mondo","0002290"
> "486","glomeruloid hemangioma","umls","C1304511"
> "486","glomeruloid hemangioma","mondo","0003172"
> "484","vascular hemostatic disease","mesh","D020141"
> "484","vascular hemostatic disease","umls","C0600502"
> "484","vascular hemostatic disease","mondo","0003159"
> "483","cavernous hemangioma","icd10cm","D18.0"
> "483","cavernous hemangioma","mesh","D006392"
> "483","cavernous hemangioma","umls","C0018920"
> "483","cavernous hemangioma","mondo","0003155"
> "482","hemangioma of peripheral nerve","umls","C1333956"
> "482","hemangioma of peripheral nerve","mondo","0003154"
> "481","obsolete central nervous system hereditary degenerative disease","umls","C0014887"
> "480","movement disease","mesh","D009069"
> "480","movement disease","umls","C0026650"
> "480","movement disease","mondo","0005395"
> "6468","mucinous cystadenofibroma","umls","C1377844"
> "6468","mucinous cystadenofibroma","mondo","0003886"
> "6469","ovarian mucinous adenofibroma","umls","C1518723"
> "6469","ovarian mucinous adenofibroma","mondo","0003887"
> "6460","large intestine lipoma","umls","C1333114"
> "6460","large intestine lipoma","mondo","0003885"
> "7747","pediatric extraocular retinoblastoma","umls","C1321870"
> "7747","pediatric extraocular retinoblastoma","mondo","0004350"
> "3923","diffuse lipomatosis","umls","C1333298"
> "3923","diffuse lipomatosis","mondo","0006539"
> "3926","mediastinal lipomatosis","umls","C1334662"
> "3926","mediastinal lipomatosis","mondo","0006578"
> "3927","pelvic lipomatosis","mesh","C535549"
> "3927","pelvic lipomatosis","umls","C0406608"
> "3927","pelvic lipomatosis","mondo","0006593"
> "3924","main bronchus cancer","icd10cm","C34.0"
> "3924","main bronchus cancer","icd9cm","162.2"
> "3924","main bronchus cancer","umls","C0153490"
> "3924","main bronchus cancer","mondo","0002811"
> "3925","steroid lipomatosis","umls","C1336506"
> "3925","steroid lipomatosis","mondo","0006612"
> "3928","adiposis dolorosa","icd10cm","E88.2"
> "3928","adiposis dolorosa","mesh","D000274"
> "3928","adiposis dolorosa","umls","C0001529"
> "3928","adiposis dolorosa","mondo","0007070"
> "8307","early invasive cervical adenocarcinoma","umls","C1333369"
> "8307","early invasive cervical adenocarcinoma","mondo","0004530"
> "8305","nonossifying fibromyxoid tumor","umls","C1335063"
> "8305","nonossifying fibromyxoid tumor","mondo","0004529"
> "8304","lymph node palisaded myofibroblastoma","umls","C1335295"
> "8304","lymph node palisaded myofibroblastoma","mondo","0004528"
> "6727","colon small cell carcinoma","umls","C1333099"
> "6727","colon small cell carcinoma","mondo","0003978"
5981,6025c15837,15844
< "12900","Mikulicz disease","icd10cm","K11.8"
< "12900","Mikulicz disease","mesh","D008882"
< "12900","Mikulicz disease","umls","C0026103"
< "12900","Mikulicz disease","mondo","0019191"
< "4780","anti-basement membrane glomerulonephritis","umls","C1332309"
< "4780","anti-basement membrane glomerulonephritis","mondo","0003136"
< "5826","breast lymphoma","umls","C0349669"
< "5826","breast lymphoma","mondo","0003661"
< "5828","endometrioid ovary carcinoma","umls","C0346163"
< "5828","endometrioid ovary carcinoma","mondo","0006335"
< "11260","rabies","icd10cm","A82"
< "11260","rabies","icd10cm","A82.9"
< "11260","rabies","icd9cm","071"
< "11260","rabies","mesh","D011818"
< "11260","rabies","umls","C0034494"
< "11260","rabies","mondo","0019173"
< "11266","hemorrhagic fever with renal syndrome","icd10cm","A98.5"
< "11266","hemorrhagic fever with renal syndrome","icd9cm","078.6"
< "11266","hemorrhagic fever with renal syndrome","mesh","D006480"
< "11266","hemorrhagic fever with renal syndrome","umls","C0019101"
< "11266","hemorrhagic fever with renal syndrome","mondo","0005784"
< "11265","trachoma","icd10cm","A71"
< "11265","trachoma","icd10cm","A71.0"
< "11265","trachoma","icd10cm","A71.1"
< "11265","trachoma","icd10cm","A71.9"
< "11265","trachoma","icd9cm","076"
< "11265","trachoma","icd9cm","076.0"
< "11265","trachoma","icd9cm","076.1"
< "11265","trachoma","icd9cm","076.9"
< "11265","trachoma","mesh","D014141"
< "11265","trachoma","umls","C0040592"
< "11265","trachoma","umls","C0153107"
< "11265","trachoma","umls","C0153108"
< "11265","trachoma","mondo","0001249"
< "7488","posterior urethra cancer","umls","C0279931"
< "7488","posterior urethra cancer","mondo","0004240"
< "3856","male reproductive organ cancer","icd10cm","C60-C63"
< "3856","male reproductive organ cancer","icd10cm","C63.9"
< "3856","male reproductive organ cancer","icd9cm","187.9"
< "3856","male reproductive organ cancer","mesh","D005834"
< "3856","male reproductive organ cancer","umls","C0017417"
< "3856","male reproductive organ cancer","umls","C0153606"
< "3856","male reproductive organ cancer","mondo","0005836"
< "3857","large cell medulloblastoma","umls","C1266180"
< "3857","large cell medulloblastoma","mondo","0002791"
---
> "9939","dacryocystocele","icd9cm","375.43"
> "9939","dacryocystocele","umls","C0155241"
> "9939","dacryocystocele","mondo","0004927"
> "9938","dacryocystitis","icd10cm","H04.30"
> "9938","dacryocystitis","icd9cm","375.30"
> "9938","dacryocystitis","mesh","D003607"
> "9938","dacryocystitis","umls","C0010930"
> "9938","dacryocystitis","mondo","0004926"
6029,6030c15848,15859
< "0080160","Cytomegalovirus retinitis","mesh","D017726"
< "0080160","Cytomegalovirus retinitis","mondo","0000878"
---
> "9937","chronic dacryocystitis","icd10cm","H04.41"
> "9937","chronic dacryocystitis","icd9cm","375.42"
> "9937","chronic dacryocystitis","umls","C0149506"
> "9937","chronic dacryocystitis","mondo","0004925"
> "9936","chronic canaliculitis","icd10cm","H04.42"
> "9936","chronic canaliculitis","icd9cm","375.41"
> "9936","chronic canaliculitis","umls","C0155240"
> "9936","chronic canaliculitis","mondo","0004924"
> "9935","chronic inflammation of lacrimal passage","icd10cm","H04.4"
> "9935","chronic inflammation of lacrimal passage","icd9cm","375.4"
> "9935","chronic inflammation of lacrimal passage","umls","C0155239"
> "9935","chronic inflammation of lacrimal passage","mondo","0004923"
6036,6039d15864
< "0080164","myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1","umls","C2827356"
< "0080164","myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1","mondo","0000881"
< "0080165","myeloid and lymphoid neoplasms associated with PDGFRA rearrangement","mondo","0000882"
< "0080166","myeloid neoplasms associated with PDGFRB rearrangement","mondo","0000883"
6045a15871,15874
> "0060850","annular pancreas","icd10cm","Q45.1"
> "0060850","annular pancreas","mesh","C536376"
> "0060850","annular pancreas","umls","C0149955"
> "0060850","annular pancreas","mondo","0008183"
6055,6056c15884,15886
< "3003","nipple neoplasm","umls","C1112166"
< "3003","nipple neoplasm","mondo","0002482"
---
> "0060854","autosomal recessive pseudohypoaldosteronism type 1","mesh","D011546"
> "0060854","autosomal recessive pseudohypoaldosteronism type 1","umls","C0268436"
> "0060854","autosomal recessive pseudohypoaldosteronism type 1","mondo","0009917"
6060,6089c15890,15897
< "5303","cervical clear cell adenocarcinoma","umls","C1332912"
< "5303","cervical clear cell adenocarcinoma","mondo","0006135"
< "0110198","Charcot-Marie-Tooth disease recessive intermediate C","icd10cm","G60.0"
< "0110198","Charcot-Marie-Tooth disease recessive intermediate C","mondo","0014154"
< "0090137","complex cortical dysplasia with other brain malformations 1","icd10cm","Q04.3"
< "0090137","complex cortical dysplasia with other brain malformations 1","mondo","0013541"
< "0070324","systemic Epstein-Barr virus-positive T-cell lymphoma of childhood","icd10cm","D47.9"
< "0070324","systemic Epstein-Barr virus-positive T-cell lymphoma of childhood","mesh","D008232"
< "12662","paracoccidioidomycosis","icd10cm","B41"
< "12662","paracoccidioidomycosis","icd10cm","B41.9"
< "12662","paracoccidioidomycosis","icd9cm","116.1"
< "12662","paracoccidioidomycosis","mesh","D010229"
< "12662","paracoccidioidomycosis","umls","C0030409"
< "12662","paracoccidioidomycosis","mondo","0005894"
< "12663","blastomycosis","icd10cm","B40"
< "12663","blastomycosis","icd10cm","B40.9"
< "12663","blastomycosis","icd9cm","116"
< "12663","blastomycosis","icd9cm","116.0"
< "12663","blastomycosis","mesh","D001759"
< "12663","blastomycosis","umls","C0005716"
< "12663","blastomycosis","mondo","0005672"
< "0060793","hypomyelinating leukodystrophy 5","icd10cm","G37.8"
< "0060793","hypomyelinating leukodystrophy 5","mondo","0012514"
< "9778","irritable bowel syndrome","kegg","05321"
< "9778","irritable bowel syndrome","icd10cm","K58"
< "9778","irritable bowel syndrome","icd10cm","K58.9"
< "9778","irritable bowel syndrome","icd9cm","564.1"
< "9778","irritable bowel syndrome","mesh","D043183"
< "9778","irritable bowel syndrome","umls","C0022104"
< "9778","irritable bowel syndrome","mondo","0005052"
---
> "6098","thalamic neoplasm","umls","C0346902"
> "6098","thalamic neoplasm","umls","C1336733"
> "6098","thalamic neoplasm","mondo","0003766"
> "6090","adult leptomeningeal melanoma","umls","C1332204"
> "6090","adult leptomeningeal melanoma","mondo","0003765"
> "12064","mediastinum neurofibroma","umls","C1334674"
> "12064","mediastinum neurofibroma","mondo","0001426"
> "0111401","congenital dyserythropoietic anemia type II","umls","C1306589"
6099,6100c15907,15915
< "0070028","APP-related cerebral amyloid angiopathy","mondo","0011583"
< "0070029","ITM2B-related cerebral amyloid angiopathy 1","mondo","0008306"
---
> "0050462","Antley-Bixler syndrome","mesh","D054882"
> "0050462","Antley-Bixler syndrome","umls","C1860042"
> "0050462","Antley-Bixler syndrome","umls","C2350233"
> "0050462","Antley-Bixler syndrome","umls","C2936791"
> "0050462","Antley-Bixler syndrome","mondo","0008803"
> "0050463","campomelic dysplasia","mesh","D055036"
> "0050463","campomelic dysplasia","umls","C1861922"
> "0050463","campomelic dysplasia","umls","C1861923"
> "0050463","campomelic dysplasia","mondo","0007251"
6103a15919,15925
> "0050465","Muir-Torre syndrome","mesh","D055653"
> "0050465","Muir-Torre syndrome","umls","C1321489"
> "0050465","Muir-Torre syndrome","mondo","0008018"
> "0050466","Loeys-Dietz syndrome","mesh","D055947"
> "0050466","Loeys-Dietz syndrome","umls","C1836635"
> "0050466","Loeys-Dietz syndrome","umls","C2697932"
> "0050466","Loeys-Dietz syndrome","mondo","0018954"
6108c15930,15933
< "0070022","autosomal recessive dyskeratosis congenita 5","mondo","0014076"
---
> "0050468","yellow nail syndrome","icd10cm","L60.5"
> "0050468","yellow nail syndrome","mesh","D056684"
> "0050468","yellow nail syndrome","umls","C0221348"
> "0050468","yellow nail syndrome","mondo","0007921"
6112,6116d15936
< "0070026","Revesz syndrome","mondo","0009990"
< "0070027","CST3-related cerebral amyloid angiopathy","mondo","0007098"
< "193","reproductive organ cancer","umls","C0178830"
< "193","reproductive organ cancer","mondo","0002149"
< "0070025","X-linked dyskeratosis congenita","mondo","0010584"
6118d15937
< "0040019","D-mannitol allergy","umls","C0571922"
6122,6126c15941,15948
< "2738","pseudoxanthoma elasticum","mesh","D011561"
< "2738","pseudoxanthoma elasticum","umls","C0033847"
< "2738","pseudoxanthoma elasticum","mondo","0009925"
< "4555","ovarian large-cell neuroendocrine carcinoma","umls","C1335174"
< "4555","ovarian large-cell neuroendocrine carcinoma","mondo","0003049"
---
> "0080016","spina bifida","mesh","D016135"
> "0080016","spina bifida","mondo","0008449"
> "3671","pericoronitis","mesh","D010497"
> "3671","pericoronitis","umls","C0031055"
> "3671","pericoronitis","mondo","0006899"
> "3677","pulmonary plasma cell granuloma","mesh","D016726"
> "3677","pulmonary plasma cell granuloma","umls","C0085269"
> "3677","pulmonary plasma cell granuloma","mondo","0006933"
6129,6131c15951,15952
< "3660","wheat allergy","mesh","D021182"
< "3660","wheat allergy","umls","C0949570"
< "3660","wheat allergy","mondo","0007021"
---
> "3675","childhood kidney cancer","umls","C1333003"
> "3675","childhood kidney cancer","mondo","0002730"
6141,6144c15962
< "0090007","immunodeficiency-centromeric instability-facial anomalies syndrome","icd10cm","D84.8"
< "0090007","immunodeficiency-centromeric instability-facial anomalies syndrome","mondo","0000133"
< "0090004","progressive pseudorheumatoid arthropathy of childhood","icd10cm","Q77.7"
< "0090004","progressive pseudorheumatoid arthropathy of childhood","mondo","0008827"
---
> "0111119","nephronophthisis 12","mondo","0013442"
6148,6194c15966,15978
< "0090002","Tietz syndrome","mondo","0007077"
< "0090003","agenesis of the corpus callosum with peripheral neuropathy","icd10cm","G60.0"
< "0090003","agenesis of the corpus callosum with peripheral neuropathy","mondo","0000902"
< "0110432","dilated cardiomyopathy 1NN","icd10cm","I42.0"
< "0110432","dilated cardiomyopathy 1NN","mondo","0014396"
< "0090001","Fraser syndrome","icd10cm","Q87.0"
< "0090001","Fraser syndrome","mesh","D058497"
< "0090001","Fraser syndrome","mondo","0009046"
< "0060795","hypomyelinating leukodystrophy 13","mondo","0014813"
< "2383","neonatal jaundice","icd10cm","P59.9"
< "2383","neonatal jaundice","mesh","D007567"
< "2383","neonatal jaundice","umls","C0022353"
< "2383","neonatal jaundice","mondo","0006584"
< "12799","mucopolysaccharidosis II","icd10cm","E76.1"
< "12799","mucopolysaccharidosis II","mesh","D016532"
< "12799","mucopolysaccharidosis II","umls","C0026705"
< "12799","mucopolysaccharidosis II","mondo","0010674"
< "2384","Wernicke encephalopathy","icd10cm","E51.2"
< "2384","Wernicke encephalopathy","mesh","D014899"
< "2384","Wernicke encephalopathy","umls","C0043121"
< "2384","Wernicke encephalopathy","mondo","0007020"
< "2409","rhinosporidiosis","icd10cm","B48.1"
< "2409","rhinosporidiosis","icd9cm","117.0"
< "2409","rhinosporidiosis","mesh","D012227"
< "2409","rhinosporidiosis","umls","C0035469"
< "2409","rhinosporidiosis","mondo","0005946"
< "2282","hidradenitis","icd9cm","705.83"
< "2282","hidradenitis","mesh","D016575"
< "2282","hidradenitis","umls","C0085160"
< "2282","hidradenitis","mondo","0002260"
< "0050269","Trichomonas vaginalis trichomoniasis","icd10cm","A59.00"
< "0050269","Trichomonas vaginalis trichomoniasis","mesh","D014247"
< "0050269","Trichomonas vaginalis trichomoniasis","mondo","0005993"
< "0070116","Meckel syndrome 2","icd10cm","Q61.9"
< "0070116","Meckel syndrome 2","mondo","0011296"
< "0070117","Meckel syndrome 3","icd10cm","Q61.9"
< "0070117","Meckel syndrome 3","mondo","0011821"
< "0070114","Niemann-Pick disease type C2","icd10cm","E75.2"
< "0070114","Niemann-Pick disease type C2","mondo","0011873"
< "0070115","Meckel syndrome 1","icd10cm","Q61.9"
< "0070115","Meckel syndrome 1","mondo","0009571"
< "0070113","Niemann-Pick disease type C1","icd10cm","E75.2"
< "0070113","Niemann-Pick disease type C1","mondo","0009757"
< "9153","variola minor","icd9cm","050.1"
< "9153","variola minor","mesh","D012899"
< "9153","variola minor","umls","C0001906"
< "9153","variola minor","mondo","0004720"
---
> "1456","glossitis","icd10cm","K14.0"
> "1456","glossitis","icd9cm","529.0"
> "1456","glossitis","mesh","D005928"
> "1456","glossitis","umls","C0017675"
> "1456","glossitis","mondo","0006771"
> "11446","sciatic neuropathy","mesh","D020426"
> "11446","sciatic neuropathy","umls","C0149940"
> "11446","sciatic neuropathy","mondo","0006960"
> "5003","eunuchism","mesh","D005058"
> "5003","eunuchism","umls","C0238117"
> "5003","eunuchism","mondo","0005758"
> "0050689","brachydactyly-syndactyly syndrome","mesh","C565193"
> "0050689","brachydactyly-syndactyly syndrome","mondo","0012544"
6201,6202c15985,15986
< "2763","ethmoid sinus squamous cell carcinoma","umls","C1333477"
< "2763","ethmoid sinus squamous cell carcinoma","mondo","0002416"
---
> "0050684","Bowen-Conradi syndrome","mesh","C537081"
> "0050684","Bowen-Conradi syndrome","mondo","0008879"
6205,6211c15989,15991
< "0110720","neuronal ceroid lipofuscinosis 4B","icd10cm","E75.4"
< "0110720","neuronal ceroid lipofuscinosis 4B","mondo","0008083"
< "9159","gas gangrene","icd10cm","A48.0"
< "9159","gas gangrene","icd9cm","040.0"
< "9159","gas gangrene","mesh","D005738"
< "9159","gas gangrene","umls","C0017105"
< "9159","gas gangrene","mondo","0005767"
---
> "0050686","organ system cancer","mesh","D009371"
> "0050686","organ system cancer","mondo","0004992"
> "0050680","Boomerang dysplasia","mondo","0007208"
6215,6219c15995,15996
< "0070118","Meckel syndrome 4","icd10cm","Q61.9"
< "0070118","Meckel syndrome 4","mondo","0012626"
< "0050450","Gitelman syndrome","mesh","D053579"
< "0050450","Gitelman syndrome","umls","C0268450"
< "0050450","Gitelman syndrome","mondo","0009904"
---
> "0050682","Athabaskan brainstem dysgenesis syndrome","mondo","0011099"
> "0050683","Bothnia retinal dystrophy","mondo","0011838"
6226,6240c16003,16025
< "0110733","neuronal ceroid lipofuscinosis 9","icd10cm","E75.4"
< "0110733","neuronal ceroid lipofuscinosis 9","mondo","0012188"
< "0110884","inflammatory bowel disease 23","mondo","0012887"
< "0110887","inflammatory bowel disease 12","mondo","0012829"
< "0110730","neuronal ceroid lipofuscinosis 4A","icd10cm","E75.4"
< "0110730","neuronal ceroid lipofuscinosis 4A","mondo","0008768"
< "0110737","neurodegeneration with brain iron accumulation 3","mesh","C548080"
< "0110737","neurodegeneration with brain iron accumulation 3","umls","C1853578"
< "0110737","neurodegeneration with brain iron accumulation 3","mondo","0011638"
< "0110736","neurodegeneration with brain iron accumulation 2b","icd10cm","G23.0"
< "0110736","neurodegeneration with brain iron accumulation 2b","mondo","0012444"
< "0110883","inflammatory bowel disease 17","mondo","0012840"
< "0110734","neurodegeneration with brain iron accumulation","mesh","C538421"
< "0110734","neurodegeneration with brain iron accumulation","umls","C2931845"
< "0110734","neurodegeneration with brain iron accumulation","mondo","0018307"
---
> "903","gastrointestinal lymphoma","umls","C0740372"
> "903","gastrointestinal lymphoma","mondo","0004699"
> "900","hepatopulmonary syndrome","icd10cm","K76.81"
> "900","hepatopulmonary syndrome","icd9cm","573.5"
> "900","hepatopulmonary syndrome","mesh","D020065"
> "900","hepatopulmonary syndrome","umls","C0600452"
> "900","hepatopulmonary syndrome","mondo","0004694"
> "901","liver lymphoma","umls","C1112746"
> "901","liver lymphoma","mondo","0004695"
> "906","peroxisomal disease","icd10cm","E71.5"
> "906","peroxisomal disease","icd10cm","E71.50"
> "906","peroxisomal disease","icd9cm","277.86"
> "906","peroxisomal disease","mesh","D018901"
> "906","peroxisomal disease","umls","C0282528"
> "906","peroxisomal disease","mondo","0019053"
> "907","liver fibroma","umls","C1333965"
> "907","liver fibroma","mondo","0004705"
> "905","Zellweger syndrome","icd10cm","E71.510"
> "905","Zellweger syndrome","mesh","D015211"
> "905","Zellweger syndrome","umls","C0043459"
> "905","Zellweger syndrome","mondo","0019609"
> "4422","malignant adenofibroma","umls","C1510778"
> "4422","malignant adenofibroma","mondo","0002991"
6244,6248d16028
< "0110739","neurodegeneration with brain iron accumulation 5","icd10cm","G23.0"
< "0110739","neurodegeneration with brain iron accumulation 5","mondo","0010476"
< "0110738","neurodegeneration with brain iron accumulation 4","icd10cm","G23.0"
< "0110738","neurodegeneration with brain iron accumulation 4","mondo","0013674"
< "0110889","inflammatory bowel disease 5","mondo","0011661"
6253,6370c16033,16050
< "1459","hypothyroidism","icd10cm","E03.9"
< "1459","hypothyroidism","icd9cm","244.9"
< "1459","hypothyroidism","mesh","D007037"
< "1459","hypothyroidism","umls","C0020676"
< "1459","hypothyroidism","mondo","0005420"
< "4959","epidermolysis bullosa dystrophica","icd10cm","Q81.2"
< "4959","epidermolysis bullosa dystrophica","mesh","D016108"
< "4959","epidermolysis bullosa dystrophica","umls","C0079294"
< "4959","epidermolysis bullosa dystrophica","mondo","0006543"
< "4085","trophoblastic neoplasm","mesh","D014328"
< "4085","trophoblastic neoplasm","umls","C0041182"
< "4085","trophoblastic neoplasm","mondo","0002872"
< "3251","prostate embryonal rhabdomyosarcoma","umls","C1335508"
< "3251","prostate embryonal rhabdomyosarcoma","mondo","0002574"
< "4952","postpoliomyelitis syndrome","icd10cm","G14"
< "4952","postpoliomyelitis syndrome","mesh","D016262"
< "4952","postpoliomyelitis syndrome","umls","C0080040"
< "4952","postpoliomyelitis syndrome","mondo","0017416"
< "0110809","hereditary spastic paraplegia 57","icd10cm","G11.4"
< "0110809","hereditary spastic paraplegia 57","mondo","0014295"
< "3252","prostate rhabdomyosarcoma","umls","C1335518"
< "3252","prostate rhabdomyosarcoma","mondo","0006389"
< "0060801","MEHMO syndrome","mesh","C537451"
< "0060801","MEHMO syndrome","umls","C1846278"
< "0060801","MEHMO syndrome","mondo","0010258"
< "0110808","hereditary spastic paraplegia 56","icd10cm","G11.4"
< "0110808","hereditary spastic paraplegia 56","mondo","0014015"
< "0060737","junctional epidermolysis bullosa Herlitz type","icd10cm","Q81.1"
< "0060737","junctional epidermolysis bullosa Herlitz type","mondo","0009182"
< "9733","renal tuberculosis","icd9cm","016.0"
< "9733","renal tuberculosis","icd9cm","016.00"
< "9733","renal tuberculosis","mesh","D014398"
< "9733","renal tuberculosis","umls","C0041328"
< "9733","renal tuberculosis","mondo","0005938"
< "0070245","primary coenzyme Q10 deficiency 8","mondo","0014754"
< "2129","atypical teratoid rhabdoid tumor","umls","C1266184"
< "2129","atypical teratoid rhabdoid tumor","mondo","0020560"
< "14037","aorta atresia","icd9cm","747.22"
< "14037","aorta atresia","umls","C0345010"
< "14037","aorta atresia","mondo","0001863"
< "9736","blue drum syndrome","icd9cm","381.02"
< "9736","blue drum syndrome","umls","C0395863"
< "9736","blue drum syndrome","mondo","0004865"
< "3254","bile duct rhabdomyosarcoma","umls","C2064434"
< "3254","bile duct rhabdomyosarcoma","mondo","0002577"
< "9280","carbamoyl phosphate synthetase I deficiency disease","mesh","D020165"
< "9280","carbamoyl phosphate synthetase I deficiency disease","umls","C0751753"
< "9280","carbamoyl phosphate synthetase I deficiency disease","mondo","0009376"
< "0070202","familial partial lipodystrophy type 2","umls","C1720860"
< "0070202","familial partial lipodystrophy type 2","mondo","0007906"
< "0080021","Schmid metaphyseal chondrodysplasia","mondo","0007983"
< "0070200","Miyoshi muscular dystrophy 2","mondo","0013221"
< "0070201","Miyoshi muscular dystrophy 3","umls","C2750076"
< "0070201","Miyoshi muscular dystrophy 3","mondo","0013222"
< "0070206","familial partial lipodystrophy type 6","mondo","0014431"
< "0070207","familial partial lipodystrophy type 1","umls","C1720859"
< "0070207","familial partial lipodystrophy type 1","mondo","0012072"
< "0070204","familial partial lipodystrophy type 3","umls","C1720861"
< "0070204","familial partial lipodystrophy type 3","mondo","0011448"
< "5138","leiomyomatosis","mesh","D018231"
< "5138","leiomyomatosis","umls","C0206654"
< "5138","leiomyomatosis","mondo","0003295"
< "10794","sphenoid sinusitis","icd10cm","J32.3"
< "10794","sphenoid sinusitis","mesh","D015524"
< "10794","sphenoid sinusitis","umls","C0037886"
< "10794","sphenoid sinusitis","mondo","0005964"
< "10027","tabes dorsalis","icd10cm","A52.11"
< "10027","tabes dorsalis","icd9cm","094.0"
< "10027","tabes dorsalis","mesh","D013606"
< "10027","tabes dorsalis","umls","C0039223"
< "10027","tabes dorsalis","mondo","0005977"
< "0070208","hereditary lymphedema IC","mondo","0013278"
< "0070209","hereditary lymphedema ID","mondo","0014393"
< "0110807","hereditary spastic paraplegia 55","icd10cm","G11.4"
< "0110807","hereditary spastic paraplegia 55","mondo","0014020"
< "10792","chronic maxillary sinusitis","icd10cm","J32.0"
< "10792","chronic maxillary sinusitis","icd9cm","473.0"
< "10792","chronic maxillary sinusitis","umls","C0008698"
< "10792","chronic maxillary sinusitis","mondo","0001122"
< "10793","chronic sphenoidal sinusitis","icd10cm","J32.3"
< "10793","chronic sphenoidal sinusitis","icd9cm","473.3"
< "10793","chronic sphenoidal sinusitis","umls","C0008712"
< "10793","chronic sphenoidal sinusitis","mondo","0001123"
< "854","collagen disease","mesh","D003095"
< "854","collagen disease","umls","C0009326"
< "854","collagen disease","mondo","0021103"
< "856","biotinidase deficiency","icd10cm","D81.810"
< "856","biotinidase deficiency","mesh","D028921"
< "856","biotinidase deficiency","umls","C0220754"
< "856","biotinidase deficiency","mondo","0009665"
< "0060837","isolated microphthalmia 5","icd10cm","Q15.8"
< "0060837","isolated microphthalmia 5","mondo","0012605"
< "0110089","asphyxiating thoracic dystrophy 5","icd10cm","Q77.2"
< "0110089","asphyxiating thoracic dystrophy 5","mondo","0013717"
< "0110088","asphyxiating thoracic dystrophy 4","icd10cm","Q77.2"
< "0110088","asphyxiating thoracic dystrophy 4","mondo","0013441"
< "0110085","asphyxiating thoracic dystrophy 1","icd10cm","Q77.2"
< "0110085","asphyxiating thoracic dystrophy 1","mondo","0008831"
< "0110084","arrhythmogenic right ventricular dysplasia 13","icd10cm","I42.8"
< "0110084","arrhythmogenic right ventricular dysplasia 13","mondo","0000908"
< "0110087","asphyxiating thoracic dystrophy 3","icd10cm","Q77.2"
< "0110087","asphyxiating thoracic dystrophy 3","mondo","0013127"
< "3459","breast carcinoma","mesh","D001943"
< "3459","breast carcinoma","umls","C0678222"
< "3459","breast carcinoma","mondo","0004989"
< "0110081","arrhythmogenic right ventricular dysplasia 10","icd10cm","I42.8"
< "0110081","arrhythmogenic right ventricular dysplasia 10","mondo","0012434"
< "859","holocarboxylase synthetase deficiency","icd10cm","D81.818"
< "859","holocarboxylase synthetase deficiency","mesh","D028922"
< "859","holocarboxylase synthetase deficiency","umls","C0268581"
< "859","holocarboxylase synthetase deficiency","mondo","0009666"
< "0110082","arrhythmogenic right ventricular dysplasia 11","icd10cm","I42.8"
< "0110082","arrhythmogenic right ventricular dysplasia 11","mondo","0012506"
< "6170","ovarian carcinosarcoma","umls","C0392998"
< "6170","ovarian carcinosarcoma","mondo","0003792"
< "0060832","Griscelli syndrome type 1","mesh","C537301"
< "0060832","Griscelli syndrome type 1","umls","C1859194"
< "0060832","Griscelli syndrome type 1","mondo","0008962"
---
> "4424","juvenile xanthogranuloma","mesh","D014972"
> "4424","juvenile xanthogranuloma","umls","C0043324"
> "4424","juvenile xanthogranuloma","mondo","0015534"
> "0050986","spinocerebellar ataxia type 40","mondo","0014475"
> "1108","esophagus melanoma","umls","C1333460"
> "1108","esophagus melanoma","mondo","0001192"
> "9550","indolent myeloma","umls","C1334169"
> "9550","indolent myeloma","mondo","0004819"
> "9553","adrenal gland disease","icd10cm","E27.9"
> "9553","adrenal gland disease","icd9cm","255"
> "9553","adrenal gland disease","icd9cm","255.9"
> "9553","adrenal gland disease","mesh","D000307"
> "9553","adrenal gland disease","umls","C0001621"
> "9553","adrenal gland disease","mondo","0005495"
> "12801","mucopolysaccharidosis III","icd10cm","E76.22"
> "12801","mucopolysaccharidosis III","mesh","D009084"
> "12801","mucopolysaccharidosis III","umls","C0026706"
> "12801","mucopolysaccharidosis III","mondo","0018937"
6381,6382d16060
< "6827","pancreatic solid pseudopapillary carcinoma","umls","C1336029"
< "6827","pancreatic solid pseudopapillary carcinoma","mondo","0018525"
6385,6447c16063,16070
< "0110067","juvenile amyotrophic lateral sclerosis with dementia","mondo","0008781"
< "0110066","amelogenesis imperfecta type 1G","icd10cm","K00.5"
< "0110066","amelogenesis imperfecta type 1G","mondo","0008771"
< "0110065","amelogenesis imperfecta type 1F","icd10cm","K00.5"
< "0110065","amelogenesis imperfecta type 1F","mondo","0014560"
< "0110064","amelogenesis imperfecta type 1H","icd10cm","K00.5"
< "0110064","amelogenesis imperfecta type 1H","mondo","0014540"
< "0110063","amelogenesis imperfecta hypomaturation type 2A5","icd10cm","K00.5"
< "0110063","amelogenesis imperfecta hypomaturation type 2A5","mondo","0014385"
< "0110062","amelogenesis imperfecta hypomaturation type 2A4","icd10cm","K00.5"
< "0110062","amelogenesis imperfecta hypomaturation type 2A4","mondo","0013906"
< "0110061","amelogenesis imperfecta hypomaturation type 2A3","icd10cm","K00.5"
< "0110061","amelogenesis imperfecta hypomaturation type 2A3","mondo","0013181"
< "0110060","amelogenesis imperfecta hypomaturation type 2A2","icd10cm","K00.5"
< "0110060","amelogenesis imperfecta hypomaturation type 2A2","mondo","0012926"
< "14784","olivopontocerebellar atrophy","mesh","D009849"
< "14784","olivopontocerebellar atrophy","umls","C0028968"
< "14784","olivopontocerebellar atrophy","mondo","0002017"
< "192","sex cord-gonadal stromal tumor","mesh","D018312"
< "192","sex cord-gonadal stromal tumor","umls","C0206724"
< "192","sex cord-gonadal stromal tumor","mondo","0006055"
< "0110069","FTDALS4","mondo","0014641"
< "0110068","FTDALS3","mondo","0014640"
< "11851","indeterminate leprosy","icd10cm","A30.0"
< "11851","indeterminate leprosy","icd9cm","030.2"
< "11851","indeterminate leprosy","umls","C0021192"
< "11851","indeterminate leprosy","mondo","0001391"
< "10242","ehrlichiosis","icd10cm","A77.4"
< "10242","ehrlichiosis","icd10cm","A77.40"
< "10242","ehrlichiosis","icd9cm","082.4"
< "10242","ehrlichiosis","icd9cm","082.40"
< "10242","ehrlichiosis","mesh","D016873"
< "10242","ehrlichiosis","umls","C0085399"
< "10242","ehrlichiosis","mondo","0016003"
< "0111042","glycogen storage disease IXa","icd10cm","E74.0"
< "0111042","glycogen storage disease IXa","mondo","0010598"
< "7004","ACTH-secreting pituitary adenoma","mesh","D049913"
< "7004","ACTH-secreting pituitary adenoma","umls","C1306214"
< "7004","ACTH-secreting pituitary adenoma","mondo","0009050"
< "0111128","focal segmental glomerulosclerosis 1","icd10cm","N04.1"
< "0111128","focal segmental glomerulosclerosis 1","mondo","0011303"
< "813","septic arthritis","icd10cm","M00"
< "813","septic arthritis","icd10cm","M00.9"
< "813","septic arthritis","icd9cm","711.0"
< "813","septic arthritis","icd9cm","711.9"
< "813","septic arthritis","icd9cm","711.90"
< "813","septic arthritis","icd9cm","711.91"
< "813","septic arthritis","icd9cm","711.92"
< "813","septic arthritis","icd9cm","711.93"
< "813","septic arthritis","icd9cm","711.94"
< "813","septic arthritis","icd9cm","711.95"
< "813","septic arthritis","icd9cm","711.96"
< "813","septic arthritis","icd9cm","711.97"
< "813","septic arthritis","mesh","D001170"
< "813","septic arthritis","umls","C0003869"
< "813","septic arthritis","umls","C0157843"
< "813","septic arthritis","umls","C0157844"
< "813","septic arthritis","umls","C0157845"
< "813","septic arthritis","umls","C0157846"
< "813","septic arthritis","umls","C0157847"
< "813","septic arthritis","umls","C0157848"
< "813","septic arthritis","umls","C0157849"
< "813","septic arthritis","mondo","0004471"
---
> "11637","accommodative spasm","icd10cm","H52.53"
> "11637","accommodative spasm","icd9cm","367.53"
> "11637","accommodative spasm","umls","C0152196"
> "11637","accommodative spasm","mondo","0001329"
> "0111044","gray platelet syndrome","icd10cm","D69.1"
> "0111044","gray platelet syndrome","mesh","D055652"
> "0111044","gray platelet syndrome","umls","C0272302"
> "0111044","gray platelet syndrome","mondo","0007686"
6452d16074
< "0040060","ketoprofen photoallergic dermatitis","umls","C0570547"
6458,6460d16079
< "0040065","quinidine allergy","umls","C0571881"
< "0040067","neomycin sulfate allergic contact dermatitis","umls","C1443961"
< "0040066","melphalan allergy","umls","C0570673"
6470,6477c16089,16101
< "0110468","autosomal recessive nonsyndromic deafness 13","icd10cm","H90.3"
< "0110468","autosomal recessive nonsyndromic deafness 13","mondo","0011286"
< "13117","paronychia","icd10cm","L03.0"
< "13117","paronychia","mesh","D010304"
< "13117","paronychia","umls","C0030578"
< "13117","paronychia","mondo","0005898"
< "0090072","hypogonadotropic hypogonadism 12 with or without anosmia","icd10cm","E23.0"
< "0090072","hypogonadotropic hypogonadism 12 with or without anosmia","mondo","0013914"
---
> "8937","Waldeyer's ring cancer","icd10cm","C14.2"
> "8937","Waldeyer's ring cancer","icd9cm","149.1"
> "8937","Waldeyer's ring cancer","umls","C0153406"
> "8937","Waldeyer's ring cancer","mondo","0004685"
> "8930","retromolar area cancer","icd10cm","C06.2"
> "8930","retromolar area cancer","icd9cm","145.6"
> "8930","retromolar area cancer","umls","C0153379"
> "8930","retromolar area cancer","mondo","0004682"
> "8931","Evans' syndrome","icd10cm","D69.41"
> "8931","Evans' syndrome","icd9cm","287.32"
> "8931","Evans' syndrome","mesh","C536380"
> "8931","Evans' syndrome","umls","C0272126"
> "8931","Evans' syndrome","mondo","0016030"
6482,6484c16106,16107
< "0110461","X-linked dilated cardiomyopathy","icd10cm","I42.0"
< "0110461","X-linked dilated cardiomyopathy","mesh","C580047"
< "0110461","X-linked dilated cardiomyopathy","mondo","0010542"
---
> "0110393","retinitis pigmentosa 66","icd10cm","H35.5"
> "0110393","retinitis pigmentosa 66","mondo","0014093"
6487,6488c16110,16111
< "0110467","autosomal recessive nonsyndromic deafness 12","icd10cm","H90.3"
< "0110467","autosomal recessive nonsyndromic deafness 12","mondo","0011067"
---
> "0110395","retinitis pigmentosa 72","icd10cm","H35.5"
> "0110395","retinitis pigmentosa 72","mondo","0014653"
6495,6530c16118,16137
< "0090070","hypogonadotropic hypogonadism","icd10cm","E23.0"
< "0090070","hypogonadotropic hypogonadism","mondo","0018555"
< "745","epididymis adenomatoid tumor","umls","C1333415"
< "745","epididymis adenomatoid tumor","mondo","0004227"
< "888","fasciolopsiasis","icd10cm","B66.5"
< "888","fasciolopsiasis","icd9cm","121.4"
< "888","fasciolopsiasis","mesh","D014201"
< "888","fasciolopsiasis","umls","C0015656"
< "888","fasciolopsiasis","mondo","0004672"
< "0070203","familial partial lipodystrophy type 5","mondo","0014098"
< "11180","non-suppurative otitis media","icd10cm","H65"
< "11180","non-suppurative otitis media","icd10cm","H65.9"
< "11180","non-suppurative otitis media","icd10cm","H65.90"
< "11180","non-suppurative otitis media","icd9cm","381.4"
< "11180","non-suppurative otitis media","umls","C0271446"
< "11180","non-suppurative otitis media","mondo","0001212"
< "14499","Fabry disease","icd10cm","E75.21"
< "14499","Fabry disease","mesh","D000795"
< "14499","Fabry disease","umls","C0002986"
< "14499","Fabry disease","mondo","0010526"
< "6898","ovarian seromucinous carcinoma","umls","C0279392"
< "6898","ovarian seromucinous carcinoma","mondo","0004031"
< "3069","astrocytoma","mesh","D001254"
< "3069","astrocytoma","umls","C0004114"
< "3069","astrocytoma","umls","C0750935"
< "3069","astrocytoma","mondo","0021636"
< "3068","glioblastoma multiforme","mesh","D005909"
< "3068","glioblastoma multiforme","umls","C0017636"
< "3068","glioblastoma multiforme","umls","C0278878"
< "3068","glioblastoma multiforme","umls","C1514422"
< "3068","glioblastoma multiforme","mondo","0018177"
< "14365","systemic primary carnitine deficiency disease","icd10cm","E71.41"
< "14365","systemic primary carnitine deficiency disease","icd9cm","277.81"
< "14365","systemic primary carnitine deficiency disease","mesh","C536778"
< "14365","systemic primary carnitine deficiency disease","umls","C0342788"
< "14365","systemic primary carnitine deficiency disease","mondo","0008919"
---
> "0070124","congenital nongoitrous hypothyroidism 2","icd10cm","E03.1"
> "0070124","congenital nongoitrous hypothyroidism 2","mondo","0024264"
> "7175","anal Buschke-Lowenstein tumor","umls","C1332278"
> "7175","anal Buschke-Lowenstein tumor","mondo","0004131"
> "7174","anus basaloid carcinoma","umls","C0280470"
> "7174","anus basaloid carcinoma","mondo","0004130"
> "7177","anal canal squamous cell carcinoma","umls","C1332262"
> "7177","anal canal squamous cell carcinoma","mondo","0004132"
> "1798","pancreatic endocrine carcinoma","icd10cm","C25.4"
> "1798","pancreatic endocrine carcinoma","icd9cm","157.4"
> "1798","pancreatic endocrine carcinoma","mesh","D018273"
> "1798","pancreatic endocrine carcinoma","umls","C1328479"
> "1798","pancreatic endocrine carcinoma","mondo","0005893"
> "7173","cloacogenic carcinoma","mesh","C563020"
> "7173","cloacogenic carcinoma","umls","C0334273"
> "7173","cloacogenic carcinoma","mondo","0004129"
> "7179","mixed eosinophil-basophil adenoma","umls","C0334312"
> "7179","mixed eosinophil-basophil adenoma","mondo","0004133"
> "0060229","Baraitser-Winter syndrome","icd10cm","Q87.0"
> "0060229","Baraitser-Winter syndrome","mondo","0017579"
6533,6538d16139
< "1056","oculocerebrorenal syndrome","icd10cm","E72.03"
< "1056","oculocerebrorenal syndrome","mesh","D009800"
< "1056","oculocerebrorenal syndrome","umls","C0028860"
< "1056","oculocerebrorenal syndrome","mondo","0010645"
< "5350","ovarian endodermal sinus tumor","umls","C0346188"
< "5350","ovarian endodermal sinus tumor","mondo","0006344"
6550a16152,16155
> "0060221","Maffucci syndrome","icd10cm","Q78.4"
> "0060221","Maffucci syndrome","mondo","0013808"
> "0060223","agraphia","icd10cm","R48.8"
> "0060223","agraphia","mondo","0000716"
6553,6555d16157
< "4267","akinetic mutism","mesh","D000405"
< "4267","akinetic mutism","umls","C0001889"
< "4267","akinetic mutism","mondo","0005640"
6558,6590c16160,16161
< "0110267","cataract 44","icd10cm","Q12.0"
< "0110267","cataract 44","mondo","0014673"
< "0110266","cataract 9 multiple types","icd10cm","Q12.0"
< "0110266","cataract 9 multiple types","mondo","0011413"
< "0110261","cataract 35","icd10cm","Q12.0"
< "0110261","cataract 35","mondo","0012260"
< "13810","familial hypercholesterolemia","icd10cm","E78.00"
< "13810","familial hypercholesterolemia","icd10cm","E78.01"
< "13810","familial hypercholesterolemia","mesh","D006938"
< "13810","familial hypercholesterolemia","umls","C0020445"
< "13810","familial hypercholesterolemia","mondo","0005439"
< "0110263","cataract 19 multiple types","icd10cm","Q12.0"
< "0110263","cataract 19 multiple types","mondo","0014111"
< "0110262","cataract 45","icd10cm","Q12.0"
< "0110262","cataract 45","mondo","0014799"
< "4910","urethra adenocarcinoma","umls","C1336885"
< "4910","urethra adenocarcinoma","mondo","0003200"
< "0110269","cataract 3 multiple types","icd10cm","Q12.0"
< "0110269","cataract 3 multiple types","mondo","0011104"
< "0110268","cataract 22 multiple types","icd10cm","Q12.0"
< "0110268","cataract 22 multiple types","mondo","0012336"
< "0070122","Meckel syndrome 8","icd10cm","Q61.9"
< "0070122","Meckel syndrome 8","mondo","0013482"
< "4313","epidermolysis bullosa acquisita","icd10cm","L12.3"
< "4313","epidermolysis bullosa acquisita","icd10cm","L12.30"
< "4313","epidermolysis bullosa acquisita","mesh","D016107"
< "4313","epidermolysis bullosa acquisita","umls","C0079293"
< "4313","epidermolysis bullosa acquisita","mondo","0018747"
< "0050462","Antley-Bixler syndrome","mesh","D054882"
< "0050462","Antley-Bixler syndrome","umls","C1860042"
< "0050462","Antley-Bixler syndrome","umls","C2350233"
< "0050462","Antley-Bixler syndrome","umls","C2936791"
< "0050462","Antley-Bixler syndrome","mondo","0008803"
---
> "1792","pancreas lymphoma","umls","C1335307"
> "1792","pancreas lymphoma","mondo","0002114"
6595,6605d16165
< "612","primary immunodeficiency disease","kegg","05340"
< "612","primary immunodeficiency disease","icd10cm","D84.9"
< "612","primary immunodeficiency disease","icd9cm","279.3"
< "612","primary immunodeficiency disease","mesh","D007153"
< "612","primary immunodeficiency disease","umls","C0021051"
< "612","primary immunodeficiency disease","mondo","0003778"
< "1271","capillary disease","icd10cm","I78"
< "1271","capillary disease","icd10cm","I78.9"
< "1271","capillary disease","icd9cm","448"
< "1271","capillary disease","umls","C0155765"
< "1271","capillary disease","mondo","0001574"
6612,6642d16171
< "614","lymphopenia","icd10cm","D72.810"
< "614","lymphopenia","icd9cm","288.51"
< "614","lymphopenia","mesh","D008231"
< "614","lymphopenia","umls","C0024312"
< "614","lymphopenia","mondo","0003783"
< "615","leukopenia","icd10cm","D72.819"
< "615","leukopenia","icd9cm","288.50"
< "615","leukopenia","mesh","D007970"
< "615","leukopenia","umls","C0023530"
< "615","leukopenia","mondo","0003785"
< "11042","Felty's syndrome","icd10cm","M05.0"
< "11042","Felty's syndrome","icd10cm","M05.00"
< "11042","Felty's syndrome","icd9cm","714.1"
< "11042","Felty's syndrome","mesh","D005258"
< "11042","Felty's syndrome","umls","C0015773"
< "11042","Felty's syndrome","mondo","0007603"
< "3405","histiocytosis","mesh","D015614"
< "3405","histiocytosis","umls","C0019618"
< "3405","histiocytosis","mondo","0002637"
< "8791","breast carcinoma in situ","icd10cm","D05"
< "8791","breast carcinoma in situ","icd10cm","D05.9"
< "8791","breast carcinoma in situ","icd9cm","233.0"
< "8791","breast carcinoma in situ","mesh","D000071960"
< "8791","breast carcinoma in situ","umls","C0154084"
< "8791","breast carcinoma in situ","mondo","0004658"
< "8792","eye carcinoma in situ","icd10cm","D09.2"
< "8792","eye carcinoma in situ","icd9cm","234.0"
< "8792","eye carcinoma in situ","umls","C0154094"
< "8792","eye carcinoma in situ","mondo","0004659"
< "0110136","Bardet-Biedl syndrome 14","icd10cm","Q87.89"
< "0110136","Bardet-Biedl syndrome 14","mondo","0014442"
6644,6645d16172
< "5288","larynx leiomyosarcoma","umls","C1334371"
< "5288","larynx leiomyosarcoma","mondo","0003374"
6650,6657d16176
< "3119","gastrointestinal system cancer","icd10cm","C26.9"
< "3119","gastrointestinal system cancer","icd9cm","239.0"
< "3119","gastrointestinal system cancer","mesh","D004067"
< "3119","gastrointestinal system cancer","mesh","D005770"
< "3119","gastrointestinal system cancer","umls","C0012243"
< "3119","gastrointestinal system cancer","umls","C0017185"
< "3119","gastrointestinal system cancer","umls","C0685938"
< "3119","gastrointestinal system cancer","mondo","0002516"
6660,6677c16179,16181
< "3117","hepatobiliary benign neoplasm","umls","C0854196"
< "3117","hepatobiliary benign neoplasm","mondo","0002514"
< "3114","serous cystadenocarcinoma","mesh","D018284"
< "3114","serous cystadenocarcinoma","umls","C0206701"
< "3114","serous cystadenocarcinoma","mondo","0005278"
< "3113","papillary carcinoma","mesh","D002291"
< "3113","papillary carcinoma","umls","C0007133"
< "3113","papillary carcinoma","mondo","0006509"
< "3112","papillary adenocarcinoma","mesh","D000231"
< "3112","papillary adenocarcinoma","umls","C0001420"
< "3112","papillary adenocarcinoma","umls","C1321863"
< "3112","papillary adenocarcinoma","mondo","0002512"
< "3110","papillary cystadenocarcinoma","mesh","D018283"
< "3110","papillary cystadenocarcinoma","umls","C0206700"
< "3110","papillary cystadenocarcinoma","mondo","0005074"
< "0060538","purpura fulminans","icd10cm","D65"
< "0060538","purpura fulminans","mesh","D055665"
< "0060538","purpura fulminans","mondo","0000809"
---
> "14768","Saethre-Chotzen syndrome","mesh","D000168"
> "14768","Saethre-Chotzen syndrome","umls","C0175699"
> "14768","Saethre-Chotzen syndrome","mondo","0007042"
6698,6731d16201
< "0060535","Warsaw breakage syndrome","mondo","0013252"
< "0060537","mitochondrial complex II deficiency","icd10cm","G71.3"
< "0060537","mitochondrial complex II deficiency","mesh","C565375"
< "0060537","mitochondrial complex II deficiency","mondo","0009641"
< "0060536","mitochondrial complex I deficiency","mesh","C537475"
< "0060536","mitochondrial complex I deficiency","umls","C2936907"
< "0060536","mitochondrial complex I deficiency","mondo","0009640"
< "0060711","autosomal recessive congenital ichthyosis 3","icd10cm","Q80.2"
< "0060711","autosomal recessive congenital ichthyosis 3","mondo","0011680"
< "0060710","autosomal recessive congenital ichthyosis 2","icd10cm","Q80.2"
< "0060710","autosomal recessive congenital ichthyosis 2","mondo","0009439"
< "0060713","autosomal recessive congenital ichthyosis 4B","icd10cm","Q80.4"
< "0060713","autosomal recessive congenital ichthyosis 4B","mondo","0009443"
< "0060712","autosomal recessive congenital ichthyosis 4A","icd10cm","Q80.2"
< "0060712","autosomal recessive congenital ichthyosis 4A","mondo","0011026"
< "0060715","autosomal recessive congenital ichthyosis 6","icd10cm","Q80.2"
< "0060715","autosomal recessive congenital ichthyosis 6","mondo","0012847"
< "0060714","autosomal recessive congenital ichthyosis 5","icd10cm","Q80.2"
< "0060714","autosomal recessive congenital ichthyosis 5","mondo","0011485"
< "0060717","autosomal recessive congenital ichthyosis 8","icd10cm","Q80.2"
< "0060717","autosomal recessive congenital ichthyosis 8","mondo","0013495"
< "0060716","autosomal recessive congenital ichthyosis 7","icd10cm","Q80.2"
< "0060716","autosomal recessive congenital ichthyosis 7","mondo","0014009"
< "0060719","autosomal recessive congenital ichthyosis 10","icd10cm","Q80.2"
< "0060719","autosomal recessive congenital ichthyosis 10","mondo","0014011"
< "0060718","autosomal recessive congenital ichthyosis 9","icd10cm","Q80.2"
< "0060718","autosomal recessive congenital ichthyosis 9","mondo","0014010"
< "8428","breast apocrine carcinoma in situ","umls","C1332315"
< "8428","breast apocrine carcinoma in situ","mondo","0004562"
< "5742","pancreatic acinar cell adenocarcinoma","umls","C0279661"
< "5742","pancreatic acinar cell adenocarcinoma","mondo","0006346"
< "5744","ovary serous adenocarcinoma","umls","C1335177"
< "5744","ovary serous adenocarcinoma","umls","C1518234"
< "5744","ovary serous adenocarcinoma","mondo","0005211"
6737,6748c16207,16213
< "5746","ovarian serous cystadenocarcinoma","umls","C0279663"
< "5746","ovarian serous cystadenocarcinoma","mondo","0006046"
< "5468","biliary papillomatosis","umls","C1266038"
< "5468","biliary papillomatosis","mondo","0003455"
< "2590","familial nephrotic syndrome","icd10cm","N04"
< "2590","familial nephrotic syndrome","mesh","C535761"
< "2590","familial nephrotic syndrome","umls","C3501848"
< "2590","familial nephrotic syndrome","mondo","0002350"
< "11302","cercarial dermatitis","icd10cm","B65.3"
< "11302","cercarial dermatitis","icd9cm","120.3"
< "11302","cercarial dermatitis","umls","C0546996"
< "11302","cercarial dermatitis","mondo","0001260"
---
> "13934","facial paralysis","icd10cm","G51.0"
> "13934","facial paralysis","mesh","D005158"
> "13934","facial paralysis","umls","C0015469"
> "13934","facial paralysis","mondo","0001835"
> "4226","endometrial stromal sarcoma","mesh","D018203"
> "4226","endometrial stromal sarcoma","umls","C0206630"
> "4226","endometrial stromal sarcoma","mondo","0006745"
6751,6753c16216,16221
< "3596","placental site trophoblastic tumor","mesh","D018245"
< "3596","placental site trophoblastic tumor","umls","C0206666"
< "3596","placental site trophoblastic tumor","mondo","0020552"
---
> "4223","pyoderma","icd10cm","L08.0"
> "4223","pyoderma","icd9cm","686.0"
> "4223","pyoderma","icd9cm","686.00"
> "4223","pyoderma","mesh","D011711"
> "4223","pyoderma","umls","C0034212"
> "4223","pyoderma","mondo","0002922"
6758a16227,16233
> "26","pancreas disease","icd10cm","K86.8"
> "26","pancreas disease","icd10cm","K86.89"
> "26","pancreas disease","icd9cm","577.8"
> "26","pancreas disease","umls","C0029771"
> "26","pancreas disease","mondo","0002356"
> "5585","Ferguson-Smith tumor","umls","C0345982"
> "5585","Ferguson-Smith tumor","mondo","0007566"
6763,6787c16238,16244
< "0060743","methylmalonic acidemia cblB type","icd10cm","E71.1"
< "0060743","methylmalonic acidemia cblB type","mondo","0009614"
< "12402","pyromania","icd10cm","F63.1"
< "12402","pyromania","icd9cm","312.33"
< "12402","pyromania","mesh","D005391"
< "12402","pyromania","umls","C0016142"
< "12402","pyromania","mondo","0001522"
< "12403","tinea pedis","icd10cm","B35.3"
< "12403","tinea pedis","icd9cm","110.4"
< "12403","tinea pedis","mesh","D014008"
< "12403","tinea pedis","umls","C0040259"
< "12403","tinea pedis","mondo","0005984"
< "12400","kleptomania","icd10cm","F63.2"
< "12400","kleptomania","icd9cm","312.32"
< "12400","kleptomania","mesh","D007174"
< "12400","kleptomania","umls","C0022734"
< "12400","kleptomania","mondo","0001520"
< "12401","intermittent explosive disorder","icd10cm","F60.3"
< "12401","intermittent explosive disorder","icd10cm","F63.81"
< "12401","intermittent explosive disorder","icd9cm","301.3"
< "12401","intermittent explosive disorder","icd9cm","312.34"
< "12401","intermittent explosive disorder","mesh","D007174"
< "12401","intermittent explosive disorder","umls","C0021776"
< "12401","intermittent explosive disorder","umls","C0152183"
< "12401","intermittent explosive disorder","mondo","0001521"
---
> "5580","pancreatic gastrinoma","umls","C1368066"
> "5580","pancreatic gastrinoma","mondo","0003525"
> "28","endocrine system disease","icd10cm","E34.9"
> "28","endocrine system disease","icd9cm","259.9"
> "28","endocrine system disease","mesh","D004700"
> "28","endocrine system disease","umls","C0014130"
> "28","endocrine system disease","mondo","0005151"
6790,6858c16247,16260
< "3187","brain oligodendroglioma","umls","C0346286"
< "3187","brain oligodendroglioma","mondo","0002544"
< "10209","extrahepatic bile duct lipoma","umls","C1333509"
< "10209","extrahepatic bile duct lipoma","mondo","0000978"
< "0060159","organic acidemia","mondo","0000688"
< "0060776","congenital diarrhea 5 with tufting enteropathy","icd10cm","P78.3"
< "0060776","congenital diarrhea 5 with tufting enteropathy","mondo","0013184"
< "5267","anus leiomyosarcoma","umls","C1332267"
< "5267","anus leiomyosarcoma","mondo","0003358"
< "9245","Alagille syndrome","icd10cm","Q44.7"
< "9245","Alagille syndrome","mesh","D016738"
< "9245","Alagille syndrome","umls","C0085280"
< "9245","Alagille syndrome","mondo","0007318"
< "3930","otitis interna","umls","C1168225"
< "3930","otitis interna","mondo","0002008"
< "10195","pleural lipoma","umls","C1335434"
< "10195","pleural lipoma","mondo","0000969"
< "8336","childhood choriocarcinoma of the ovary","umls","C1332987"
< "8336","childhood choriocarcinoma of the ovary","mondo","0004535"
< "8337","appendicitis","icd10cm","K37"
< "8337","appendicitis","icd9cm","540-543.99"
< "8337","appendicitis","icd9cm","541"
< "8337","appendicitis","mesh","D001064"
< "8337","appendicitis","umls","C0003615"
< "8337","appendicitis","mondo","0005649"
< "0060319","cardiac arrest","icd10cm","I46"
< "0060319","cardiac arrest","icd9cm","427.5"
< "0060319","cardiac arrest","mesh","D006323"
< "0060319","cardiac arrest","umls","C0018790"
< "0060319","cardiac arrest","umls","C0600228"
< "0060319","cardiac arrest","mondo","0000745"
< "9246","cerebral amyloid angiopathy","mesh","D028243"
< "9246","cerebral amyloid angiopathy","umls","C0268393"
< "9246","cerebral amyloid angiopathy","umls","C1510489"
< "9246","cerebral amyloid angiopathy","umls","C1527338"
< "9246","cerebral amyloid angiopathy","umls","C1956349"
< "9246","cerebral amyloid angiopathy","mondo","0005620"
< "6713","cerebrovascular disease","icd10cm","I60-I69"
< "6713","cerebrovascular disease","icd10cm","I63.9"
< "6713","cerebrovascular disease","icd10cm","I67.9"
< "6713","cerebrovascular disease","icd9cm","430-438.99"
< "6713","cerebrovascular disease","icd9cm","437.9"
< "6713","cerebrovascular disease","mesh","D002561"
< "6713","cerebrovascular disease","mesh","D020521"
< "6713","cerebrovascular disease","umls","C0007820"
< "6713","cerebrovascular disease","umls","C0038454"
< "6713","cerebrovascular disease","mondo","0011057"
< "5262","heart sarcoma","umls","C0238152"
< "5262","heart sarcoma","mondo","0003354"
< "12140","Chagas disease","kegg","05142"
< "12140","Chagas disease","icd9cm","086.2"
< "12140","Chagas disease","mesh","D014355"
< "12140","Chagas disease","umls","C0007932"
< "12140","Chagas disease","mondo","0001444"
< "9903","meibomian cyst","icd10cm","H00.1"
< "9903","meibomian cyst","icd9cm","373.2"
< "9903","meibomian cyst","mesh","D017043"
< "9903","meibomian cyst","umls","C0007933"
< "9903","meibomian cyst","mondo","0005844"
< "12531","von Willebrand's disease","icd10cm","D68.0"
< "12531","von Willebrand's disease","icd10cm","D69.8"
< "12531","von Willebrand's disease","icd9cm","286.4"
< "12531","von Willebrand's disease","mesh","D014842"
< "12531","von Willebrand's disease","umls","C0042974"
< "12531","von Willebrand's disease","mondo","0019565"
< "9909","hordeolum","icd10cm","H00.01"
< "9909","hordeolum","mesh","D006726"
< "9909","hordeolum","umls","C0019917"
< "9909","hordeolum","mondo","0005800"
---
> "1068","juvenile glaucoma","mondo","0020367"
> "13689","prostate calculus","icd10cm","N42.0"
> "13689","prostate calculus","icd9cm","602.0"
> "13689","prostate calculus","umls","C0149525"
> "13689","prostate calculus","mondo","0001776"
> "11277","Plummer's disease","icd10cm","E05.2"
> "11277","Plummer's disease","icd9cm","242.3"
> "11277","Plummer's disease","umls","C0342127"
> "11277","Plummer's disease","mondo","0001252"
> "13687","chronic duodenal ileus","icd10cm","K31.5"
> "13687","chronic duodenal ileus","icd9cm","537.2"
> "13687","chronic duodenal ileus","umls","C0156087"
> "13687","chronic duodenal ileus","mondo","0001775"
> "0110660","congenital myasthenic syndrome 12","mondo","0012518"
6863,6866d16264
< "5696","larynx liposarcoma","umls","C1334372"
< "5696","larynx liposarcoma","mondo","0003588"
< "5697","liposarcoma of the ovary","umls","C1335165"
< "5697","liposarcoma of the ovary","mondo","0003589"
6871,6948c16269,16297
< "5699","kidney liposarcoma","umls","C1335745"
< "5699","kidney liposarcoma","mondo","0003591"
< "4465","papillary renal cell carcinoma","mesh","C538614"
< "4465","papillary renal cell carcinoma","mesh","D002292"
< "4465","papillary renal cell carcinoma","umls","C1306837"
< "4465","papillary renal cell carcinoma","umls","C1336078"
< "4465","papillary renal cell carcinoma","mondo","0017884"
< "0110862","congenital stationary night blindness autosomal dominant 1","mondo","0012498"
< "0060316","orofaciodigital syndrome I","icd10cm","Q87.0"
< "0060316","orofaciodigital syndrome I","mesh","D009958"
< "0060316","orofaciodigital syndrome I","umls","C0026363"
< "0060316","orofaciodigital syndrome I","umls","C0029294"
< "0060316","orofaciodigital syndrome I","umls","C1510460"
< "0060316","orofaciodigital syndrome I","mondo","0010702"
< "0080158","herpes simplex virus keratitis","mesh","D007635"
< "0080158","herpes simplex virus keratitis","mesh","D016849"
< "0080158","herpes simplex virus keratitis","mondo","0015288"
< "0110482","autosomal recessive nonsyndromic deafness 24","icd10cm","H90.3"
< "0110482","autosomal recessive nonsyndromic deafness 24","mondo","0012602"
< "0080156","X-linked adrenal hypoplasia congenita","mondo","0010264"
< "5306","bladder clear cell adenocarcinoma","umls","C1332557"
< "5306","bladder clear cell adenocarcinoma","mondo","0003386"
< "0080327","multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly","mondo","0009359"
< "0110851","rhizomelic chondrodysplasia punctata type 1","icd10cm","Q77.3"
< "0110851","rhizomelic chondrodysplasia punctata type 1","mondo","0008972"
< "5268","myxoid leiomyosarcoma","mesh","D007890"
< "5268","myxoid leiomyosarcoma","umls","C0205816"
< "5268","myxoid leiomyosarcoma","mondo","0003359"
< "0070046","Coffin-Siris syndrome 4","mondo","0013821"
< "4045","muscle cancer","icd10cm","C49"
< "4045","muscle cancer","mesh","D009217"
< "4045","muscle cancer","mesh","D019042"
< "4045","muscle cancer","umls","C0027095"
< "4045","muscle cancer","umls","C0684743"
< "4045","muscle cancer","mondo","0005864"
< "4047","liver rhabdomyosarcoma","umls","C1333975"
< "4047","liver rhabdomyosarcoma","mondo","0002849"
< "0110354","retinitis pigmentosa 19","icd10cm","H35.5"
< "0110354","retinitis pigmentosa 19","mondo","0011137"
< "1556","arthus reaction","icd10cm","T78.41"
< "1556","arthus reaction","icd9cm","995.21"
< "1556","arthus reaction","mesh","D001183"
< "1556","arthus reaction","umls","C0003907"
< "1556","arthus reaction","mondo","0006660"
< "0110357","retinitis pigmentosa 35","icd10cm","H35.5"
< "0110357","retinitis pigmentosa 35","mondo","0012463"
< "13282","intestinal tuberculosis","icd9cm","014.8"
< "13282","intestinal tuberculosis","umls","C0152724"
< "13282","intestinal tuberculosis","mondo","0001678"
< "13078","eumycotic mycetoma","icd10cm","B47"
< "13078","eumycotic mycetoma","icd10cm","B47.9"
< "13078","eumycotic mycetoma","mesh","D008271"
< "13078","eumycotic mycetoma","umls","C0024449"
< "13078","eumycotic mycetoma","mondo","0005757"
< "0110356","retinitis pigmentosa 18","icd10cm","H35.5"
< "0110356","retinitis pigmentosa 18","mondo","0011075"
< "10871","age related macular degeneration","icd10cm","H35.30"
< "10871","age related macular degeneration","icd9cm","362.50"
< "10871","age related macular degeneration","mesh","D008268"
< "10871","age related macular degeneration","umls","C0242383"
< "10871","age related macular degeneration","mondo","0005150"
< "0110351","osteogenesis imperfecta type 11","icd10cm","Q78.0"
< "0110351","osteogenesis imperfecta type 11","mondo","0012592"
< "0070043","autosomal dominant non-syndromic intellectual disability 13","mondo","0013805"
< "0080026","otospondylomegaepiphyseal dysplasia","mondo","0008975"
< "3664","mast cell neoplasm","icd10cm","D47.09"
< "3664","mast cell neoplasm","umls","C0334664"
< "3664","mast cell neoplasm","mondo","0002724"
< "594","panic disorder","icd10cm","F41.0"
< "594","panic disorder","mesh","D016584"
< "594","panic disorder","umls","C0030319"
< "594","panic disorder","mondo","0005383"
< "0110421","late-adult onset retinitis pigmentosa","icd10cm","H35.5"
< "0110421","late-adult onset retinitis pigmentosa","mondo","0009984"
< "13368","tinea profunda","umls","C1279621"
< "13368","tinea profunda","mondo","0001698"
< "0110721","neuronal ceroid lipofuscinosis 1","icd10cm","E75.4"
< "0110721","neuronal ceroid lipofuscinosis 1","mondo","0009744"
---
> "1063","interstitial nephritis","icd10cm","N12"
> "1063","interstitial nephritis","mesh","D009395"
> "1063","interstitial nephritis","umls","C0027707"
> "1063","interstitial nephritis","mondo","0001085"
> "1062","Fanconi syndrome","mesh","D005198"
> "1062","Fanconi syndrome","umls","C0015624"
> "1062","Fanconi syndrome","umls","C0341703"
> "1062","Fanconi syndrome","mondo","0001083"
> "13790","acute tympanitis","icd10cm","H73.0"
> "13790","acute tympanitis","icd10cm","H73.00"
> "13790","acute tympanitis","icd10cm","H73.009"
> "13790","acute tympanitis","icd9cm","384.00"
> "13790","acute tympanitis","umls","C0155460"
> "13790","acute tympanitis","mondo","0001802"
> "1067","open-angle glaucoma","icd10cm","H40.1"
> "1067","open-angle glaucoma","icd10cm","H40.10"
> "1067","open-angle glaucoma","icd10cm","H40.13"
> "1067","open-angle glaucoma","icd9cm","365.1"
> "1067","open-angle glaucoma","icd9cm","365.10"
> "1067","open-angle glaucoma","icd9cm","365.13"
> "1067","open-angle glaucoma","mesh","D005902"
> "1067","open-angle glaucoma","umls","C0017612"
> "1067","open-angle glaucoma","mondo","0005338"
> "1066","residual stage of open angle glaucoma","icd10cm","H40.15"
> "1066","residual stage of open angle glaucoma","icd9cm","365.15"
> "1066","residual stage of open angle glaucoma","umls","C0154944"
> "1066","residual stage of open angle glaucoma","mondo","0001094"
> "7479","duodenal somatostatinoma","umls","C1333320"
> "7479","duodenal somatostatinoma","mondo","0004236"
6953,7028c16302,16324
< "0050454","periventricular nodular heterotopia","mesh","D054091"
< "0050454","periventricular nodular heterotopia","umls","C1848213"
< "0050454","periventricular nodular heterotopia","umls","C1868720"
< "0050454","periventricular nodular heterotopia","mondo","0020341"
< "0050457","Sertoli cell-only syndrome","mesh","D054331"
< "0050457","Sertoli cell-only syndrome","umls","C1384583"
< "0050457","Sertoli cell-only syndrome","mondo","0010595"
< "0050456","Buruli ulcer disease","icd10cm","A31.1"
< "0050456","Buruli ulcer disease","mesh","D054312"
< "0050456","Buruli ulcer disease","umls","C0085568"
< "0050456","Buruli ulcer disease","mondo","0000327"
< "0050451","Brugada syndrome","icd10cm","I49.8"
< "0050451","Brugada syndrome","mesh","D053840"
< "0050451","Brugada syndrome","umls","C1142166"
< "0050451","Brugada syndrome","umls","C1721096"
< "0050451","Brugada syndrome","mondo","0015263"
< "0060883","intestinal hypomagnesemia 1","icd10cm","E83.4"
< "0060883","intestinal hypomagnesemia 1","mondo","0011176"
< "0050452","mevalonic aciduria","icd10cm","M04.1"
< "0050452","mevalonic aciduria","mesh","D054078"
< "0050452","mevalonic aciduria","umls","C0342731"
< "0050452","mevalonic aciduria","umls","C0398691"
< "0050452","mevalonic aciduria","umls","C1959626"
< "0050452","mevalonic aciduria","mondo","0012481"
< "0110891","inflammatory bowel disease 3","mondo","0011471"
< "4541","nominal aphasia","mesh","D000849"
< "4541","nominal aphasia","umls","C0003113"
< "4541","nominal aphasia","mondo","0003039"
< "0080020","Jansen's metaphyseal chondrodysplasia","mondo","0007982"
< "4920","eccrine adenocarcinoma","umls","C1266066"
< "4920","eccrine adenocarcinoma","mondo","0024240"
< "0060884","renal hypomagnesemia 6","icd10cm","E83.4"
< "0060884","renal hypomagnesemia 6","mondo","0013480"
< "1664","pineoblastoma","mesh","D010871"
< "1664","pineoblastoma","umls","C0205898"
< "1664","pineoblastoma","mondo","0016722"
< "0111129","focal segmental glomerulosclerosis 2","icd10cm","N04.1"
< "0111129","focal segmental glomerulosclerosis 2","mondo","0011390"
< "0090101","lethal congenital glycogen storage disease of heart","icd10cm","E74.0+"
< "0090101","lethal congenital glycogen storage disease of heart","icd10cm","G73.6*"
< "0090101","lethal congenital glycogen storage disease of heart","mondo","0009867"
< "0111125","nephronophthisis 18","mondo","0014374"
< "0111124","nephronophthisis 16","mondo","0014158"
< "0111127","nephronophthisis 20","mondo","0014997"
< "0060886","osteopathia striata with cranial sclerosis","mesh","C536053"
< "0060886","osteopathia striata with cranial sclerosis","umls","C0432268"
< "0060886","osteopathia striata with cranial sclerosis","mondo","0010310"
< "0111121","nephronophthisis 13","mondo","0013718"
< "0111120","nephronophthisis 9","mondo","0013444"
< "0111123","nephronophthisis 15","mondo","0013917"
< "2571","Langerhans-cell histiocytosis","icd10cm","C96.0"
< "2571","Langerhans-cell histiocytosis","icd10cm","C96.5"
< "2571","Langerhans-cell histiocytosis","icd10cm","C96.6"
< "2571","Langerhans-cell histiocytosis","icd9cm","202.5"
< "2571","Langerhans-cell histiocytosis","mesh","C538636"
< "2571","Langerhans-cell histiocytosis","mesh","D006646"
< "2571","Langerhans-cell histiocytosis","umls","C0019621"
< "2571","Langerhans-cell histiocytosis","umls","C0023381"
< "2571","Langerhans-cell histiocytosis","mondo","0018310"
< "5283","vagina leiomyosarcoma","umls","C1336940"
< "5283","vagina leiomyosarcoma","mondo","0003369"
< "0110728","neuronal ceroid lipofuscinosis 5","icd10cm","E75.4"
< "0110728","neuronal ceroid lipofuscinosis 5","mondo","0009745"
< "2378","relapsing-remitting multiple sclerosis","mesh","D020529"
< "2378","relapsing-remitting multiple sclerosis","umls","C0751967"
< "2378","relapsing-remitting multiple sclerosis","mondo","0005314"
< "0050214","Lambert-Eaton myasthenic syndrome","icd10cm","G70.80"
< "0050214","Lambert-Eaton myasthenic syndrome","icd9cm","358.3"
< "0050214","Lambert-Eaton myasthenic syndrome","mesh","D015624"
< "0050214","Lambert-Eaton myasthenic syndrome","umls","C0022972"
< "0050214","Lambert-Eaton myasthenic syndrome","mondo","0018556"
< "2377","multiple sclerosis","icd10cm","G35"
< "2377","multiple sclerosis","icd9cm","340"
< "2377","multiple sclerosis","mesh","D009103"
< "2377","multiple sclerosis","umls","C0026769"
< "2377","multiple sclerosis","mondo","0005301"
---
> "2282","hidradenitis","icd9cm","705.83"
> "2282","hidradenitis","mesh","D016575"
> "2282","hidradenitis","umls","C0085160"
> "2282","hidradenitis","mondo","0002260"
> "2283","keratopathy","umls","C0235270"
> "2283","keratopathy","mondo","0002261"
> "0111220","centronuclear myopathy 2","umls","C0410204"
> "2286","capillary lymphangioma","umls","C1333176"
> "2286","capillary lymphangioma","mondo","0002262"
> "0111225","centronuclear myopathy X-linked","umls","C0410203"
> "2059","vulvar disease","mesh","D014845"
> "2059","vulvar disease","umls","C0042994"
> "2059","vulvar disease","mondo","0002187"
> "10907","microcephaly","icd10cm","Q02"
> "10907","microcephaly","icd9cm","742.1"
> "10907","microcephaly","mesh","D008831"
> "10907","microcephaly","umls","C0025958"
> "10907","microcephaly","mondo","0001149"
> "13444","glanders","icd10cm","A24.0"
> "13444","glanders","icd9cm","024"
> "13444","glanders","mesh","D005896"
> "13444","glanders","umls","C0017589"
> "13444","glanders","mondo","0005774"
7034,7045c16330
< "2373","hereditary elliptocytosis","icd10cm","D58.1"
< "2373","hereditary elliptocytosis","icd9cm","282.1"
< "2373","hereditary elliptocytosis","mesh","D004612"
< "2373","hereditary elliptocytosis","umls","C0013902"
< "2373","hereditary elliptocytosis","mondo","0017319"
< "9120","amyloidosis","icd10cm","E85"
< "9120","amyloidosis","icd10cm","E85.9"
< "9120","amyloidosis","icd9cm","277.3"
< "9120","amyloidosis","icd9cm","277.30"
< "9120","amyloidosis","mesh","D000686"
< "9120","amyloidosis","umls","C0002726"
< "9120","amyloidosis","mondo","0019065"
---
> "0070163","spermatogenic failure 21","mondo","0054725"
7065a16351,16352
> "10655","lipoma of colon","umls","C0940607"
> "10655","lipoma of colon","mondo","0001091"
7068,7098c16355,16374
< "5032","pineal gland cancer","icd10cm","C75.3"
< "5032","pineal gland cancer","icd9cm","194.4"
< "5032","pineal gland cancer","mesh","D010871"
< "5032","pineal gland cancer","umls","C0031941"
< "5032","pineal gland cancer","umls","C0153655"
< "5032","pineal gland cancer","umls","C1412004"
< "5032","pineal gland cancer","mondo","0003249"
< "10652","Alzheimer's disease","kegg","05010"
< "10652","Alzheimer's disease","icd10cm","G30"
< "10652","Alzheimer's disease","icd10cm","G30.9"
< "10652","Alzheimer's disease","icd9cm","331.0"
< "10652","Alzheimer's disease","mesh","D000544"
< "10652","Alzheimer's disease","umls","C0002395"
< "10652","Alzheimer's disease","mondo","0004975"
< "0050529","adult spinal muscular atrophy","mondo","0010056"
< "13026","lobomycosis","icd10cm","B48.0"
< "13026","lobomycosis","icd9cm","116.2"
< "13026","lobomycosis","mesh","D060368"
< "13026","lobomycosis","umls","C0152066"
< "13026","lobomycosis","mondo","0001616"
< "870","neuropathy","icd10cm","G62.9"
< "870","neuropathy","umls","C0442874"
< "870","neuropathy","mondo","0005244"
< "4926","bronchiolo-alveolar adenocarcinoma","mesh","D002282"
< "4926","bronchiolo-alveolar adenocarcinoma","umls","C0007120"
< "4926","bronchiolo-alveolar adenocarcinoma","mondo","0004991"
< "0050523","adult T-cell leukemia","icd10cm","C91.5"
< "0050523","adult T-cell leukemia","icd10cm","C91.50"
< "0050523","adult T-cell leukemia","mesh","D015459"
< "0050523","adult T-cell leukemia","umls","C0023493"
< "0050523","adult T-cell leukemia","mondo","0019471"
---
> "10303","sialadenitis","icd10cm","K11.2"
> "10303","sialadenitis","icd10cm","K11.20"
> "10303","sialadenitis","icd9cm","527.2"
> "10303","sialadenitis","mesh","D012793"
> "10303","sialadenitis","umls","C0037023"
> "10303","sialadenitis","mondo","0006969"
> "10302","parotid disease","mesh","D010305"
> "10302","parotid disease","umls","C0030579"
> "10302","parotid disease","mondo","0005899"
> "10301","parotitis","icd10cm","K11.2"
> "10301","parotitis","mesh","D010309"
> "10301","parotitis","umls","C0030583"
> "10301","parotitis","mondo","0005900"
> "10300","Raynaud disease","icd10cm","I73.0"
> "10300","Raynaud disease","mesh","D011928"
> "10300","Raynaud disease","umls","C0034734"
> "10300","Raynaud disease","mondo","0008364"
> "7912","mixed oligodendroglioma-astrocytoma","mesh","D009837"
> "7912","mixed oligodendroglioma-astrocytoma","umls","C0280793"
> "7912","mixed oligodendroglioma-astrocytoma","mondo","0016702"
7101,7129c16377,16391
< "4439","central nervous system germ cell tumor","umls","C1332880"
< "4439","central nervous system germ cell tumor","mondo","0003000"
< "0050524","maturity-onset diabetes of the young","kegg","04950"
< "0050524","maturity-onset diabetes of the young","icd10cm","E11.8"
< "0050524","maturity-onset diabetes of the young","mondo","0018911"
< "0050526","Gamstorp-Wohlfart syndrome","mondo","0007646"
< "0090107","autosomal dominant hypocalcemia 1","mondo","0011013"
< "0110893","inflammatory bowel disease 13","mondo","0012831"
< "0110722","neuronal ceroid lipofuscinosis 7","icd10cm","E75.4"
< "0110722","neuronal ceroid lipofuscinosis 7","mondo","0012588"
< "0090104","Huntington's disease-like 2","icd10cm","G10"
< "0090104","Huntington's disease-like 2","mondo","0011671"
< "0110896","inflammatory bowel disease 16","mondo","0012838"
< "0110897","inflammatory bowel disease 15","mondo","0012837"
< "0060887","ossification of the posterior longitudinal ligament of spine","mondo","0011230"
< "0110727","neuronal ceroid lipofuscinosis 13","icd10cm","E75.4"
< "0110727","neuronal ceroid lipofuscinosis 13","mondo","0014147"
< "0060889","prune belly syndrome","icd10cm","Q79.4"
< "0060889","prune belly syndrome","mesh","D011535"
< "0060889","prune belly syndrome","mondo","0007032"
< "0110729","neuronal ceroid lipofuscinosis 6","icd10cm","E75.4"
< "0110729","neuronal ceroid lipofuscinosis 6","mondo","0011144"
< "0110898","inflammatory bowel disease 20","mondo","0012852"
< "0110899","inflammatory bowel disease 28","mondo","0013153"
< "4948","gallbladder carcinoma","umls","C0235782"
< "4948","gallbladder carcinoma","mondo","0003220"
< "0090109","autosomal dominant hypocalcemia","icd10cm","E20.8"
< "0090109","autosomal dominant hypocalcemia","mondo","0018543"
< "0090108","autosomal dominant hypocalcemia 2","mondo","0014146"
---
> "7915","cervical spinal canal and spinal cord meningioma","umls","C1332916"
> "7915","cervical spinal canal and spinal cord meningioma","mondo","0004396"
> "10629","microphthalmia","icd10cm","Q11.2"
> "10629","microphthalmia","icd9cm","743.1"
> "10629","microphthalmia","icd9cm","743.10"
> "10629","microphthalmia","icd9cm","743.11"
> "10629","microphthalmia","mesh","D008850"
> "10629","microphthalmia","umls","C0026010"
> "10629","microphthalmia","mondo","0021129"
> "6284","epicardium lipoma","umls","C1333411"
> "6284","epicardium lipoma","mondo","0003840"
> "6285","heart lipoma","umls","C1332849"
> "6285","heart lipoma","mondo","0003841"
> "6286","childhood cerebellar astrocytic neoplasm","umls","C0278594"
> "6286","childhood cerebellar astrocytic neoplasm","mondo","0003842"
7133,7134d16394
< "6043","ciliary body spindle cell melanoma","umls","C1333052"
< "6043","ciliary body spindle cell melanoma","mondo","0003746"
7138,7140d16397
< "7983","breast malignant eccrine spiradenoma","umls","C1334565"
< "7983","breast malignant eccrine spiradenoma","mondo","0004420"
< "0110870","congenital stationary night blindness 1A","mondo","0010690"
7144,7164c16401,16403
< "2112","cystoisosporiasis","icd10cm","A07.3"
< "2112","cystoisosporiasis","mesh","D021865"
< "2112","cystoisosporiasis","umls","C0311386"
< "2112","cystoisosporiasis","mondo","0018769"
< "2113","coccidiosis","mesh","D003048"
< "2113","coccidiosis","umls","C0009187"
< "2113","coccidiosis","mondo","0005707"
< "2115","B cell deficiency","icd9cm","279.03"
< "2115","B cell deficiency","umls","C0154276"
< "2115","B cell deficiency","mondo","0002211"
< "4152","chondroid chordoma","umls","C1266173"
< "4152","chondroid chordoma","mondo","0006145"
< "2621","autonomic nervous system neoplasm","umls","C1332356"
< "2621","autonomic nervous system neoplasm","mondo","0002366"
< "6148","nasal cavity carcinoma in situ","icd10cm","D02.3"
< "6148","nasal cavity carcinoma in situ","umls","C0347095"
< "6148","nasal cavity carcinoma in situ","mondo","0003784"
< "10612","allergic urticaria","icd10cm","L50.0"
< "10612","allergic urticaria","icd9cm","708.0"
< "10612","allergic urticaria","umls","C0149526"
< "10612","allergic urticaria","mondo","0006526"
---
> "9407","strictly posterior acute myocardial infarction","icd9cm","410.60"
> "9407","strictly posterior acute myocardial infarction","umls","C0155652"
> "9407","strictly posterior acute myocardial infarction","mondo","0004780"
7174,7199c16413,16431
< "263","kidney cancer","icd10cm","C64"
< "263","kidney cancer","icd9cm","189.0"
< "263","kidney cancer","mesh","D007680"
< "263","kidney cancer","umls","C0022665"
< "263","kidney cancer","umls","C0494158"
< "263","kidney cancer","umls","C0740457"
< "263","kidney cancer","mondo","0002367"
< "1910","vaginal yolk sac tumor","umls","C1336945"
< "1910","vaginal yolk sac tumor","mondo","0002143"
< "0040100","Hirata disease","umls","C0854359"
< "0040100","Hirata disease","mondo","0018465"
< "3284","thymic carcinoma","mesh","D013945"
< "3284","thymic carcinoma","umls","C0205969"
< "3284","thymic carcinoma","mondo","0006451"
< "10017","multiple endocrine neoplasia type 1","icd10cm","E31.21"
< "10017","multiple endocrine neoplasia type 1","icd9cm","258.01"
< "10017","multiple endocrine neoplasia type 1","mesh","D018761"
< "10017","multiple endocrine neoplasia type 1","umls","C0025267"
< "10017","multiple endocrine neoplasia type 1","mondo","0007540"
< "10016","multiple endocrine neoplasia type 2B","icd10cm","E31.23"
< "10016","multiple endocrine neoplasia type 2B","icd9cm","258.03"
< "10016","multiple endocrine neoplasia type 2B","mesh","D018814"
< "10016","multiple endocrine neoplasia type 2B","umls","C0025269"
< "10016","multiple endocrine neoplasia type 2B","mondo","0008082"
< "0110098","atopic dermatitis 2","mondo","0011596"
< "0110099","atopic dermatitis 3","mondo","0011597"
---
> "11629","pelvic muscle wasting","icd10cm","N81.84"
> "11629","pelvic muscle wasting","icd9cm","618.83"
> "11629","pelvic muscle wasting","umls","C1456255"
> "11629","pelvic muscle wasting","mondo","0001327"
> "0050148","laryngotracheitis","icd10cm","J04"
> "0050148","laryngotracheitis","icd10cm","J04.2"
> "0050148","laryngotracheitis","icd10cm","J37.1"
> "0050148","laryngotracheitis","icd9cm","464"
> "0050148","laryngotracheitis","icd9cm","464.2"
> "0050148","laryngotracheitis","icd9cm","476.1"
> "0050148","laryngotracheitis","umls","C0155811"
> "0050148","laryngotracheitis","umls","C0155837"
> "0050148","laryngotracheitis","mondo","0000263"
> "869","cholesteatoma","icd10cm","H71.9"
> "869","cholesteatoma","icd10cm","H71.90"
> "869","cholesteatoma","icd9cm","385.30"
> "869","cholesteatoma","mesh","D002781"
> "869","cholesteatoma","umls","C0008373"
> "869","cholesteatoma","mondo","0006530"
7202,7207c16434,16439
< "5830","cervical endometrioid adenocarcinoma","umls","C1332913"
< "5830","cervical endometrioid adenocarcinoma","mondo","0003665"
< "0110092","short-rib thoracic dysplasia 6 with or without polydactyly","icd10cm","Q77.2"
< "0110092","short-rib thoracic dysplasia 6 with or without polydactyly","mondo","0009894"
< "0110093","short-rib thoracic dysplasia 13 with or without polydactyly","icd10cm","Q77.2"
< "0110093","short-rib thoracic dysplasia 13 with or without polydactyly","mondo","0014577"
---
> "3448","penis Paget's disease","umls","C0221286"
> "3448","penis Paget's disease","mondo","0002653"
> "3445","scrotal carcinoma","umls","C1370468"
> "3445","scrotal carcinoma","mondo","0002650"
> "3444","scrotum Paget's disease","umls","C0238330"
> "3444","scrotum Paget's disease","mondo","0002649"
7210,7212c16442,16445
< "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","icd10cm","Q77.2"
< "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","icd10cm","Q87.5"
< "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","mondo","0014284"
---
> "862","diplegia of upper limb","icd10cm","G83.0"
> "862","diplegia of upper limb","icd9cm","344.2"
> "862","diplegia of upper limb","umls","C0154701"
> "862","diplegia of upper limb","mondo","0004618"
7216,7221c16449,16458
< "0110097","short-rib thoracic dysplasia 9 with or without polydactyly","icd10cm","Q87.5"
< "0110097","short-rib thoracic dysplasia 9 with or without polydactyly","mondo","0009964"
< "0110094","short-rib thoracic dysplasia 8 with or without polydactyly","icd10cm","Q77.2"
< "0110094","short-rib thoracic dysplasia 8 with or without polydactyly","mondo","0014214"
< "0110095","short-rib thoracic dysplasia 11 with or without polydactyly","icd10cm","Q77.2"
< "0110095","short-rib thoracic dysplasia 11 with or without polydactyly","mondo","0014287"
---
> "864","phlebitis","icd10cm","I80"
> "864","phlebitis","mesh","D010689"
> "864","phlebitis","umls","C0031542"
> "864","phlebitis","mondo","0004625"
> "3443","mammary Paget's disease","umls","C1368019"
> "3443","mammary Paget's disease","mondo","0002648"
> "866","vein disease","icd10cm","I82"
> "866","vein disease","icd9cm","453"
> "866","vein disease","umls","C0155774"
> "866","vein disease","mondo","0004634"
7233,7255c16470,16487
< "0110658","congenital myasthenic syndrome 15","mondo","0014542"
< "0110659","congenital myasthenic syndrome 7","mondo","0014468"
< "262","kidney hemangiopericytoma","umls","C0346256"
< "262","kidney hemangiopericytoma","mondo","0002365"
< "0110654","long QT syndrome 13","icd10cm","I45.8"
< "0110654","long QT syndrome 13","mondo","0013279"
< "0110655","long QT syndrome 14","icd10cm","I45.8"
< "0110655","long QT syndrome 14","mondo","0014548"
< "0110656","long QT syndrome 15","icd10cm","I45.8"
< "0110656","long QT syndrome 15","mondo","0014550"
< "0110657","congenital myasthenic syndrome 8","mondo","0014052"
< "0110650","long QT syndrome 9","icd10cm","I45.8"
< "0110650","long QT syndrome 9","mondo","0012736"
< "0110651","long QT syndrome 10","icd10cm","I45.8"
< "0110651","long QT syndrome 10","mondo","0012737"
< "12347","osteogenesis imperfecta","icd10cm","Q78.0"
< "12347","osteogenesis imperfecta","icd9cm","756.51"
< "12347","osteogenesis imperfecta","mesh","D010013"
< "12347","osteogenesis imperfecta","umls","C0023931"
< "12347","osteogenesis imperfecta","umls","C0029434"
< "12347","osteogenesis imperfecta","mondo","0019019"
< "0110653","long QT syndrome 12","icd10cm","I45.8"
< "0110653","long QT syndrome 12","mondo","0013062"
---
> "2752","glycogen storage disease II","icd10cm","E74.02"
> "2752","glycogen storage disease II","mesh","D006009"
> "2752","glycogen storage disease II","umls","C0017921"
> "2752","glycogen storage disease II","mondo","0009290"
> "2021","placenta cancer","icd10cm","C58"
> "2021","placenta cancer","icd9cm","181"
> "2021","placenta cancer","umls","C0153572"
> "2021","placenta cancer","mondo","0002178"
> "2750","glycogen storage disease IV","icd10cm","E74.09"
> "2750","glycogen storage disease IV","mesh","D006011"
> "2750","glycogen storage disease IV","umls","C0017923"
> "2750","glycogen storage disease IV","mondo","0009292"
> "2751","glycogen storage disease VIII","mesh","D006015"
> "2751","glycogen storage disease VIII","umls","C0017927"
> "2751","glycogen storage disease VIII","mondo","0006772"
> "0111259","postaxial acrofacial dysostosis","umls","C0265257"
> "0111258","pentosuria","mesh","C536652"
> "0111258","pentosuria","umls","C0268162"
7270,7274c16502,16503
< "885","fascioliasis","icd10cm","B66.3"
< "885","fascioliasis","icd9cm","121.3"
< "885","fascioliasis","mesh","D005211"
< "885","fascioliasis","umls","C0015652"
< "885","fascioliasis","mondo","0004668"
---
> "0110072","arrhythmogenic right ventricular dysplasia 3","icd10cm","I42.8"
> "0110072","arrhythmogenic right ventricular dysplasia 3","mondo","0011188"
7277,7282d16505
< "14791","Leber congenital amaurosis","mesh","D057130"
< "14791","Leber congenital amaurosis","umls","C0339527"
< "14791","Leber congenital amaurosis","mondo","0018998"
< "14793","hypohidrotic ectodermal dysplasia","mesh","D053358"
< "14793","hypohidrotic ectodermal dysplasia","umls","C0162359"
< "14793","hypohidrotic ectodermal dysplasia","mondo","0016535"
7287,7290d16509
< "14796","Dubowitz syndrome","icd10cm","Q87.1"
< "14796","Dubowitz syndrome","mesh","C535718"
< "14796","Dubowitz syndrome","umls","C0175691"
< "14796","Dubowitz syndrome","mondo","0009124"
7292a16512,16515
> "10151","malignant neoplasm of short bones of lower limb","icd10cm","C40.3"
> "10151","malignant neoplasm of short bones of lower limb","icd9cm","170.8"
> "10151","malignant neoplasm of short bones of lower limb","umls","C0153518"
> "10151","malignant neoplasm of short bones of lower limb","mondo","0000953"
7295a16519,16523
> "5213","chronic inflammatory demyelinating polyradiculoneuropathy","icd10cm","G61.81"
> "5213","chronic inflammatory demyelinating polyradiculoneuropathy","icd9cm","357.81"
> "5213","chronic inflammatory demyelinating polyradiculoneuropathy","mesh","D020277"
> "5213","chronic inflammatory demyelinating polyradiculoneuropathy","umls","C0393819"
> "5213","chronic inflammatory demyelinating polyradiculoneuropathy","mondo","0006702"
7298,7343c16526,16533
< "14026","folic acid deficiency anemia","icd10cm","D52"
< "14026","folic acid deficiency anemia","icd10cm","D52.9"
< "14026","folic acid deficiency anemia","icd9cm","281.2"
< "14026","folic acid deficiency anemia","umls","C0151482"
< "14026","folic acid deficiency anemia","mondo","0001860"
< "0110226","Brugada syndrome 9","icd10cm","I49.8"
< "0110226","Brugada syndrome 9","mondo","0014621"
< "9053","bladder carcinoma in situ","icd10cm","D09.0"
< "9053","bladder carcinoma in situ","icd9cm","233.7"
< "9053","bladder carcinoma in situ","umls","C0154091"
< "9053","bladder carcinoma in situ","mondo","0004703"
< "14150","spinal cord lymphoma","umls","C1336044"
< "14150","spinal cord lymphoma","mondo","0001892"
< "0110386","retinitis pigmentosa 42","icd10cm","H35.5"
< "0110386","retinitis pigmentosa 42","mondo","0013052"
< "0110387","retinitis pigmentosa 9","icd10cm","H35.5"
< "0110387","retinitis pigmentosa 9","mondo","0008378"
< "0110384","retinitis pigmentosa 25","icd10cm","H35.5"
< "0110384","retinitis pigmentosa 25","mondo","0011272"
< "0110385","retinitis pigmentosa 63","icd10cm","H35.5"
< "0110385","retinitis pigmentosa 63","mondo","0013780"
< "0110382","retinitis pigmentosa 48","icd10cm","H35.5"
< "0110382","retinitis pigmentosa 48","mondo","0013447"
< "0110383","retinitis pigmentosa 7","icd10cm","H35.5"
< "0110383","retinitis pigmentosa 7","mondo","0011974"
< "0110380","retinitis pigmentosa 62","icd10cm","H35.5"
< "0110380","retinitis pigmentosa 62","mondo","0013611"
< "0110381","retinitis pigmentosa 14","icd10cm","H35.5"
< "0110381","retinitis pigmentosa 14","mondo","0010827"
< "0070303","multiple epiphyseal dysplasia 1","mesh","C535501"
< "0070303","multiple epiphyseal dysplasia 1","umls","C1838280"
< "0070303","multiple epiphyseal dysplasia 1","mondo","0007561"
< "0070302","multiple epiphyseal dysplasia 7","mondo","0054680"
< "0070301","multiple epiphyseal dysplasia 6","mondo","0013591"
< "0070300","multiple epiphyseal dysplasia 4","mesh","C535504"
< "0070300","multiple epiphyseal dysplasia 4","umls","C1847593"
< "0070300","multiple epiphyseal dysplasia 4","mondo","0009189"
< "0070307","craniolenticulosutural dysplasia","mondo","0011911"
< "0110388","retinitis pigmentosa 10","icd10cm","H35.5"
< "0110388","retinitis pigmentosa 10","mondo","0008379"
< "0070304","multiple epiphyseal dysplasia 3","mondo","0010964"
< "8927","learning disability","icd10cm","F81.9"
< "8927","learning disability","mesh","D007859"
< "8927","learning disability","umls","C0023186"
< "8927","learning disability","umls","C0751265"
< "8927","learning disability","mondo","0004681"
---
> "14155","acute retrobulbar neuritis","icd9cm","377.32"
> "14155","acute retrobulbar neuritis","umls","C0155301"
> "14155","acute retrobulbar neuritis","mondo","0001895"
> "14152","spinal cord sarcoma","umls","C1336049"
> "14152","spinal cord sarcoma","mondo","0001894"
> "0040078","gallamine allergy","umls","C0571145"
> "14151","spinal cord melanoma","umls","C1336045"
> "14151","spinal cord melanoma","mondo","0001893"
7350,7355c16540,16541
< "8924","autoimmune thrombocytopenic purpura","icd10cm","D69.3"
< "8924","autoimmune thrombocytopenic purpura","icd9cm","287.31"
< "8924","autoimmune thrombocytopenic purpura","mesh","D016553"
< "8924","autoimmune thrombocytopenic purpura","umls","C0398650"
< "8924","autoimmune thrombocytopenic purpura","mondo","0008558"
< "0110683","congenital myasthenic syndrome 18","mondo","0014590"
---
> "8427","retinal melanoma","umls","C0853394"
> "8427","retinal melanoma","mondo","0004561"
7358,7377c16544,16554
< "8920","leukoplakia of vagina","icd10cm","N89.4"
< "8920","leukoplakia of vagina","icd9cm","623.1"
< "8920","leukoplakia of vagina","umls","C0156385"
< "8920","leukoplakia of vagina","mondo","0004679"
< "0110470","autosomal recessive nonsyndromic deafness 15","icd10cm","H90.3"
< "0110470","autosomal recessive nonsyndromic deafness 15","mondo","0011160"
< "0110471","autosomal recessive nonsyndromic deafness 16","icd10cm","H90.3"
< "0110471","autosomal recessive nonsyndromic deafness 16","mondo","0011364"
< "0110472","autosomal recessive nonsyndromic deafness 17","icd10cm","H90.3"
< "0110472","autosomal recessive nonsyndromic deafness 17","mondo","0011279"
< "0110473","autosomal recessive nonsyndromic deafness 18A","icd10cm","H90.3"
< "0110473","autosomal recessive nonsyndromic deafness 18A","mondo","0011192"
< "0110474","autosomal recessive nonsyndromic deafness 18B","icd10cm","H90.3"
< "0110474","autosomal recessive nonsyndromic deafness 18B","mondo","0013985"
< "0110475","autosomal recessive nonsyndromic deafness 1A","icd10cm","H90.3"
< "0110475","autosomal recessive nonsyndromic deafness 1A","mondo","0009076"
< "0110476","autosomal recessive nonsyndromic deafness 1B","icd10cm","H90.3"
< "0110476","autosomal recessive nonsyndromic deafness 1B","mondo","0012977"
< "0110477","autosomal recessive nonsyndromic deafness 2","icd10cm","H90.3"
< "0110477","autosomal recessive nonsyndromic deafness 2","mondo","0010807"
---
> "13100","intracranial vasospasm","mesh","D020301"
> "13100","intracranial vasospasm","umls","C0751895"
> "13100","intracranial vasospasm","mondo","0006812"
> "14484","sporotrichosis","icd10cm","B42"
> "14484","sporotrichosis","icd10cm","B42.9"
> "14484","sporotrichosis","icd9cm","117.1"
> "14484","sporotrichosis","mesh","D013174"
> "14484","sporotrichosis","umls","C0038034"
> "14484","sporotrichosis","mondo","0005968"
> "0111553","spondyloepiphyseal dysplasia Maroteaux type","mesh","C563218"
> "0111553","spondyloepiphyseal dysplasia Maroteaux type","umls","C3159322"
7383,7406c16560,16567
< "77","gastrointestinal system disease","icd10cm","K92.9"
< "77","gastrointestinal system disease","icd9cm","520-579.99"
< "77","gastrointestinal system disease","mesh","D004066"
< "77","gastrointestinal system disease","umls","C0012242"
< "77","gastrointestinal system disease","mondo","0004335"
< "76","stomach disease","mesh","D013272"
< "76","stomach disease","umls","C0038354"
< "76","stomach disease","mondo","0004298"
< "2978","carbohydrate metabolic disorder","mesh","D002239"
< "2978","carbohydrate metabolic disorder","umls","C0007001"
< "2978","carbohydrate metabolic disorder","mondo","0019214"
< "74","hematopoietic system disease","icd10cm","D75.9"
< "74","hematopoietic system disease","icd9cm","280-289.99"
< "74","hematopoietic system disease","icd9cm","289.9"
< "74","hematopoietic system disease","mesh","D006402"
< "74","hematopoietic system disease","umls","C0018939"
< "74","hematopoietic system disease","mondo","0005570"
< "0050840","cervical dystonia","mondo","0000481"
< "0050841","focal hand dystonia","icd9cm","333.84"
< "0050841","focal hand dystonia","umls","C0154676"
< "0050841","focal hand dystonia","mondo","0000482"
< "655","inherited metabolic disorder","mesh","D008661"
< "655","inherited metabolic disorder","umls","C0025521"
< "655","inherited metabolic disorder","mondo","0019052"
---
> "14483","chorea gravidarum","mesh","D020150"
> "14483","chorea gravidarum","umls","C0264746"
> "14483","chorea gravidarum","mondo","0001976"
> "0111554","spondylometaphyseal dysplasia Kozlowski type","mesh","C535797"
> "0111554","spondylometaphyseal dysplasia Kozlowski type","umls","C0265280"
> "14489","ureteral lymphoma","umls","C1336876"
> "14489","ureteral lymphoma","mondo","0001977"
> "0060543","Hermansky-Pudlak syndrome 5","mondo","0013557"
7427,7653c16588,16665
< "5362","focal epithelial hyperplasia","mesh","D017573"
< "5362","focal epithelial hyperplasia","umls","C0206067"
< "5362","focal epithelial hyperplasia","mondo","0009237"
< "0060238","Van Maldergem syndrome","mesh","C536530"
< "0060238","Van Maldergem syndrome","umls","C1832390"
< "0060238","Van Maldergem syndrome","mondo","0017813"
< "1040","chronic lymphocytic leukemia","icd10cm","C91.1"
< "1040","chronic lymphocytic leukemia","icd10cm","C91.10"
< "1040","chronic lymphocytic leukemia","icd9cm","204.1"
< "1040","chronic lymphocytic leukemia","mesh","D015451"
< "1040","chronic lymphocytic leukemia","umls","C0023434"
< "1040","chronic lymphocytic leukemia","mondo","0004948"
< "65","connective tissue disease","mesh","D003240"
< "65","connective tissue disease","umls","C0009782"
< "65","connective tissue disease","mondo","0003900"
< "0060232","branchiootic syndrome","icd10cm","Q87.0"
< "0060232","branchiootic syndrome","mondo","0018878"
< "0060233","cardiofaciocutaneous syndrome","icd10cm","Q87.8"
< "0060233","cardiofaciocutaneous syndrome","mondo","0015280"
< "5368","Wolffian duct adenocarcinoma","umls","C1516419"
< "5368","Wolffian duct adenocarcinoma","mondo","0003410"
< "0060231","Bruck syndrome","icd10cm","M21.8"
< "0060231","Bruck syndrome","mondo","0017195"
< "0060236","xanthinuria","mesh","C562584"
< "0060236","xanthinuria","mesh","C566358"
< "0060236","xanthinuria","umls","C0268118"
< "0060236","xanthinuria","umls","C1863688"
< "0060236","xanthinuria","mondo","0018106"
< "0060237","Warburg micro syndrome","mesh","C536681"
< "0060237","Warburg micro syndrome","umls","C1838625"
< "0060237","Warburg micro syndrome","mondo","0016649"
< "0060234","Carpenter syndrome","mesh","C563187"
< "0060234","Carpenter syndrome","umls","C1275078"
< "0060234","Carpenter syndrome","mondo","0019012"
< "0060235","carnitine palmitoyltransferase II deficiency","mesh","C535589"
< "0060235","carnitine palmitoyltransferase II deficiency","umls","C0342790"
< "0060235","carnitine palmitoyltransferase II deficiency","mondo","0015515"
< "0110272","cataract 40","icd10cm","Q12.0"
< "0110272","cataract 40","mondo","0010544"
< "0110270","cataract 17 multiple types","icd10cm","Q12.0"
< "0110270","cataract 17 multiple types","mondo","0012688"
< "0110271","cataract 23","icd10cm","Q12.0"
< "0110271","cataract 23","mondo","0012489"
< "0110276","autosomal recessive limb-girdle muscular dystrophy type 2B","icd10cm","G71.0"
< "0110276","autosomal recessive limb-girdle muscular dystrophy type 2B","mondo","0009676"
< "0110277","autosomal recessive limb-girdle muscular dystrophy type 2C","icd10cm","G71.0"
< "0110277","autosomal recessive limb-girdle muscular dystrophy type 2C","mondo","0009677"
< "0110275","autosomal recessive limb-girdle muscular dystrophy type 2A","icd10cm","G71.0"
< "0110275","autosomal recessive limb-girdle muscular dystrophy type 2A","mondo","0009675"
< "0110278","autosomal recessive limb-girdle muscular dystrophy type 2D","icd10cm","G71.0"
< "0110278","autosomal recessive limb-girdle muscular dystrophy type 2D","mondo","0011968"
< "0110279","autosomal recessive limb-girdle muscular dystrophy type 2E","icd10cm","G71.0"
< "0110279","autosomal recessive limb-girdle muscular dystrophy type 2E","mondo","0011423"
< "3523","brain stem infarction","mesh","D020526"
< "3523","brain stem infarction","umls","C0521542"
< "3523","brain stem infarction","mondo","0006686"
< "4301","vulva basal cell carcinoma","umls","C1336977"
< "4301","vulva basal cell carcinoma","mondo","0002955"
< "4624","Ollier disease","icd10cm","Q78.4"
< "4624","Ollier disease","mesh","D004687"
< "4624","Ollier disease","umls","C0024454"
< "4624","Ollier disease","mondo","0008145"
< "4305","bone giant cell tumor","mesh","D018212"
< "4305","bone giant cell tumor","umls","C0206638"
< "4305","bone giant cell tumor","mondo","0005674"
< "668","myositis ossificans","mesh","D009221"
< "668","myositis ossificans","umls","C0027122"
< "668","myositis ossificans","mondo","0003964"
< "7332","esophageal tuberculosis","icd9cm","017.8"
< "7332","esophageal tuberculosis","umls","C0152902"
< "7332","esophageal tuberculosis","mondo","0004189"
< "0050548","hereditary sensory neuropathy","mondo","0015364"
< "0110754","type 1 diabetes mellitus 17","icd10cm","E10"
< "0110754","type 1 diabetes mellitus 17","mondo","0011302"
< "1911","endodermal sinus tumor","mesh","D018240"
< "1911","endodermal sinus tumor","umls","C0014145"
< "1911","endodermal sinus tumor","mondo","0005744"
< "11054","urinary bladder cancer","kegg","05219"
< "11054","urinary bladder cancer","icd10cm","C67"
< "11054","urinary bladder cancer","icd10cm","C67.9"
< "11054","urinary bladder cancer","icd9cm","188"
< "11054","urinary bladder cancer","icd9cm","188.9"
< "11054","urinary bladder cancer","mesh","D001749"
< "11054","urinary bladder cancer","umls","C0005684"
< "11054","urinary bladder cancer","umls","C0005695"
< "11054","urinary bladder cancer","mondo","0001187"
< "11055","pasteurellosis","icd10cm","A28.0"
< "11055","pasteurellosis","icd9cm","027.2"
< "11055","pasteurellosis","mesh","D010326"
< "11055","pasteurellosis","umls","C0030636"
< "11055","pasteurellosis","mondo","0005901"
< "0060849","osteoporosis-pseudoglioma syndrome","mesh","C536063"
< "0060849","osteoporosis-pseudoglioma syndrome","umls","C0432252"
< "0060849","osteoporosis-pseudoglioma syndrome","mondo","0009820"
< "8781","rubella","icd10cm","B06"
< "8781","rubella","icd10cm","B06.9"
< "8781","rubella","icd9cm","056"
< "8781","rubella","mesh","D012409"
< "8781","rubella","umls","C0035920"
< "8781","rubella","mondo","0004656"
< "9620","vesicoureteral reflux","icd10cm","N13.7"
< "9620","vesicoureteral reflux","icd10cm","N13.70"
< "9620","vesicoureteral reflux","icd9cm","593.7"
< "9620","vesicoureteral reflux","mesh","D014718"
< "9620","vesicoureteral reflux","umls","C0042580"
< "9620","vesicoureteral reflux","mondo","0006007"
< "9230","pompholyx","icd9cm","705.81"
< "9230","pompholyx","mesh","D011146"
< "9230","pompholyx","umls","C0032633"
< "9230","pompholyx","mondo","0006540"
< "3121","gallbladder cancer","icd10cm","C23"
< "3121","gallbladder cancer","icd9cm","156.0"
< "3121","gallbladder cancer","mesh","D005706"
< "3121","gallbladder cancer","umls","C0016978"
< "3121","gallbladder cancer","umls","C0153452"
< "3121","gallbladder cancer","umls","C0278806"
< "3121","gallbladder cancer","mondo","0005411"
< "8659","chickenpox","icd10cm","B01"
< "8659","chickenpox","icd10cm","B01.9"
< "8659","chickenpox","icd9cm","052"
< "8659","chickenpox","mesh","D002644"
< "8659","chickenpox","umls","C0008049"
< "8659","chickenpox","mondo","0005700"
< "7608","parathyroid adenoma","mesh","D010282"
< "7608","parathyroid adenoma","umls","C0262587"
< "7608","parathyroid adenoma","mondo","0006890"
< "0070216","familial hyperinsulinemic hypoglycemia 3","mondo","0011236"
< "1467","serous labyrinthitis","icd9cm","386.31"
< "1467","serous labyrinthitis","umls","C0155504"
< "1467","serous labyrinthitis","mondo","0002006"
< "1461","cholesterol embolism","icd10cm","I75"
< "1461","cholesterol embolism","icd9cm","445"
< "1461","cholesterol embolism","mesh","D017700"
< "1461","cholesterol embolism","umls","C0149649"
< "1461","cholesterol embolism","mondo","0005568"
< "0060833","Griscelli syndrome type 2","mesh","C537302"
< "0060833","Griscelli syndrome type 2","umls","C1868679"
< "0060833","Griscelli syndrome type 2","mondo","0011872"
< "8432","polycythemia","icd10cm","D75.1"
< "8432","polycythemia","mesh","D011086"
< "8432","polycythemia","umls","C0032461"
< "8432","polycythemia","mondo","0005571"
< "0060384","acrofacial dysostosis, Catania type","mesh","C538182"
< "0060384","acrofacial dysostosis, Catania type","umls","C2931762"
< "0060384","acrofacial dysostosis, Catania type","mondo","0007045"
< "0060708","lymphoproliferative syndrome 2","icd10cm","D47.9"
< "0060708","lymphoproliferative syndrome 2","mondo","0014054"
< "13560","subserous uterine fibroid","icd10cm","D25.2"
< "13560","subserous uterine fibroid","icd9cm","218.2"
< "13560","subserous uterine fibroid","umls","C0153995"
< "13560","subserous uterine fibroid","mondo","0001745"
< "0060706","X-linked lymphoproliferative syndrome 2","icd10cm","D82.3"
< "0060706","X-linked lymphoproliferative syndrome 2","mondo","0010385"
< "0060707","lymphoproliferative syndrome 1","icd10cm","D47.9"
< "0060707","lymphoproliferative syndrome 1","mondo","0013081"
< "0060705","X-linked lymphoproliferative syndrome 1","icd10cm","D82.3"
< "0060705","X-linked lymphoproliferative syndrome 1","mondo","0010627"
< "0060702","familial hypocalciuric hypercalcemia 3","icd10cm","E83.5"
< "0060702","familial hypocalciuric hypercalcemia 3","mondo","0010926"
< "0060703","Muenke Syndrome","mesh","C537369"
< "0060703","Muenke Syndrome","umls","C1864436"
< "0060703","Muenke Syndrome","mondo","0011274"
< "0060700","familial hypocalciuric hypercalcemia 1","icd10cm","E83.5"
< "0060700","familial hypocalciuric hypercalcemia 1","mondo","0007791"
< "0060701","familial hypocalciuric hypercalcemia 2","icd10cm","E83.5"
< "0060701","familial hypocalciuric hypercalcemia 2","mondo","0007792"
< "5751","pancreatic serous cystadenocarcinoma","umls","C1335315"
< "5751","pancreatic serous cystadenocarcinoma","mondo","0003630"
< "5750","uterine corpus serous adenocarcinoma","umls","C1336921"
< "5750","uterine corpus serous adenocarcinoma","mondo","0003629"
< "0070211","hereditary lymphedema IB","mondo","0012765"
< "4239","alveolar soft part sarcoma","mesh","D018234"
< "4239","alveolar soft part sarcoma","umls","C0206657"
< "4239","alveolar soft part sarcoma","umls","C0279544"
< "4239","alveolar soft part sarcoma","umls","C0279985"
< "4239","alveolar soft part sarcoma","mondo","0011655"
< "0060260","ptosis","icd10cm","H02.4"
< "0060260","ptosis","icd10cm","H02.40"
< "0060260","ptosis","icd10cm","H02.409"
< "0060260","ptosis","icd9cm","374.3"
< "0060260","ptosis","icd9cm","374.30"
< "0060260","ptosis","mesh","D001763"
< "0060260","ptosis","umls","C0005745"
< "0060260","ptosis","mondo","0000728"
< "0110312","hypertrophic cardiomyopathy 6","mondo","0010946"
< "4236","carcinosarcoma","mesh","D002296"
< "4236","carcinosarcoma","mesh","D018199"
< "4236","carcinosarcoma","mesh","D018200"
< "4236","carcinosarcoma","umls","C0007140"
< "4236","carcinosarcoma","umls","C0206627"
< "4236","carcinosarcoma","umls","C1334603"
< "4236","carcinosarcoma","mondo","0002928"
< "0060842","isolated microphthalmia 3","icd10cm","Q11.0"
< "0060842","isolated microphthalmia 3","mondo","0012604"
< "4233","clear cell sarcoma","mesh","D018227"
< "4233","clear cell sarcoma","umls","C0206651"
< "4233","clear cell sarcoma","umls","C1332198"
< "4233","clear cell sarcoma","mondo","0002926"
< "9828","neonatal abstinence syndrome","icd10cm","P96.1"
< "9828","neonatal abstinence syndrome","icd9cm","779.5"
< "9828","neonatal abstinence syndrome","mesh","D009357"
< "9828","neonatal abstinence syndrome","umls","C0027609"
< "9828","neonatal abstinence syndrome","umls","C1332133"
< "9828","neonatal abstinence syndrome","mondo","0005566"
< "5593","gastric papillary adenocarcinoma","umls","C1333785"
< "5593","gastric papillary adenocarcinoma","mondo","0006228"
< "5592","breast papillary carcinoma","umls","C1336027"
< "5592","breast papillary carcinoma","mondo","0003532"
< "5597","fallopian tube papillary adenocarcinoma","umls","C1333595"
< "5597","fallopian tube papillary adenocarcinoma","mondo","0003535"
< "10349","solitary cyst of breast","icd10cm","N60.0"
< "10349","solitary cyst of breast","icd10cm","N60.09"
< "10349","solitary cyst of breast","icd9cm","610.0"
< "10349","solitary cyst of breast","umls","C0037619"
< "10349","solitary cyst of breast","mondo","0001009"
< "6126","anal canal carcinoma","mesh","C563020"
< "6126","anal canal carcinoma","umls","C0563211"
< "6126","anal canal carcinoma","mondo","0007108"
< "6067","ovarian mucinous neoplasm","umls","C1335168"
< "6067","ovarian mucinous neoplasm","umls","C1518233"
< "6067","ovarian mucinous neoplasm","mondo","0003756"
< "8731","carotid body cancer","icd10cm","C75.4"
< "8731","carotid body cancer","icd9cm","194.5"
< "8731","carotid body cancer","umls","C0153656"
< "8731","carotid body cancer","mondo","0004650"
< "0110090","short-rib thoracic dysplasia 7 with or without polydactyly","icd10cm","Q77.2"
< "0110090","short-rib thoracic dysplasia 7 with or without polydactyly","mondo","0013569"
---
> "7632","Cowper gland carcinoma","umls","C1516284"
> "7632","Cowper gland carcinoma","mondo","0004311"
> "7633","macular holes","mesh","D012167"
> "7633","macular holes","umls","C0024441"
> "7633","macular holes","mondo","0006843"
> "0111563","Sturge-Weber syndrome","mesh","D013341"
> "0111563","Sturge-Weber syndrome","umls","C0038505"
> "9622","kidney hypertrophy","icd10cm","N28.81"
> "9622","kidney hypertrophy","icd9cm","593.1"
> "9622","kidney hypertrophy","umls","C0156259"
> "9622","kidney hypertrophy","mondo","0004841"
> "10011","thyroid lymphoma","umls","C1336753"
> "10011","thyroid lymphoma","mondo","0019962"
> "1312","focal segmental glomerulosclerosis","mesh","D005923"
> "1312","focal segmental glomerulosclerosis","umls","C0017668"
> "1312","focal segmental glomerulosclerosis","mondo","0005363"
> "1319","brain cancer","icd10cm","C71"
> "1319","brain cancer","icd10cm","C71.9"
> "1319","brain cancer","icd9cm","191"
> "1319","brain cancer","icd9cm","191.9"
> "1319","brain cancer","icd9cm","239.6"
> "1319","brain cancer","mesh","D001932"
> "1319","brain cancer","umls","C0006118"
> "1319","brain cancer","umls","C0153633"
> "1319","brain cancer","umls","C0220624"
> "1319","brain cancer","umls","C0750974"
> "1319","brain cancer","umls","C0750979"
> "1319","brain cancer","umls","C1334557"
> "1319","brain cancer","mondo","0001657"
> "6446","ceruminous adenocarcinoma","umls","C0334353"
> "6446","ceruminous adenocarcinoma","mondo","0003880"
> "6917","predominantly cortical thymoma","umls","C1266094"
> "6917","predominantly cortical thymoma","mondo","0006459"
> "218","ascending colon cancer","icd10cm","C18.2"
> "218","ascending colon cancer","icd9cm","153.6"
> "218","ascending colon cancer","umls","C0153439"
> "218","ascending colon cancer","mondo","0002238"
> "219","colon cancer","icd10cm","C18"
> "219","colon cancer","icd10cm","C18.9"
> "219","colon cancer","icd9cm","153"
> "219","colon cancer","icd9cm","153.9"
> "219","colon cancer","mesh","D003110"
> "219","colon cancer","umls","C0007102"
> "219","colon cancer","mondo","0021063"
> "6448","vulvar apocrine adenocarcinoma","mondo","0003881"
> "10017","multiple endocrine neoplasia type 1","icd10cm","E31.21"
> "10017","multiple endocrine neoplasia type 1","icd9cm","258.01"
> "10017","multiple endocrine neoplasia type 1","mesh","D018761"
> "10017","multiple endocrine neoplasia type 1","umls","C0025267"
> "10017","multiple endocrine neoplasia type 1","mondo","0007540"
> "0060412","chromosome 1q41-q42 deletion syndrome","icd10cm","Q93.5"
> "0060412","chromosome 1q41-q42 deletion syndrome","mondo","0012927"
> "7729","acinar cell cystadenocarcinoma","umls","C1266087"
> "7729","acinar cell cystadenocarcinoma","mondo","0004343"
> "0060410","chromosome 1p36 deletion syndrome","mesh","C535362"
> "0060410","chromosome 1p36 deletion syndrome","umls","C1842870"
> "0060410","chromosome 1p36 deletion syndrome","mondo","0011929"
> "0060411","chromosome 1q21.1 deletion syndrome","icd10cm","Q93.5"
> "0060411","chromosome 1q21.1 deletion syndrome","mondo","0012914"
> "0060416","chromosome 2q31.2 deletion syndrome","mondo","0012870"
> "0060417","3p- syndrome","icd10cm","Q93.5"
> "0060417","3p- syndrome","mondo","0013424"
> "0060414","chromosome 2p12-p11.2 deletion syndrome","mondo","0013309"
> "0060415","chromosome 2p16.1-p15 deletion syndrome","icd10cm","Q93.5"
> "0060415","chromosome 2p16.1-p15 deletion syndrome","mondo","0012916"
> "0060418","chromosome 3q13.31 deletion syndrome","mesh","C536808"
> "0060418","chromosome 3q13.31 deletion syndrome","umls","C2931338"
> "0060418","chromosome 3q13.31 deletion syndrome","mondo","0014185"
> "0060419","chromosome 3q29 microdeletion syndrome","mesh","C567184"
> "0060419","chromosome 3q29 microdeletion syndrome","mondo","0012269"
> "0060148","simultanagnosia","mondo","0000678"
> "7725","epilepsy with generalized tonic-clonic seizures","mesh","D004830"
> "7725","epilepsy with generalized tonic-clonic seizures","umls","C0014549"
> "7725","epilepsy with generalized tonic-clonic seizures","mondo","0005754"
> "11781","regular astigmatism","icd10cm","H52.22"
> "11781","regular astigmatism","icd9cm","367.21"
> "11781","regular astigmatism","umls","C0152193"
> "11781","regular astigmatism","mondo","0001364"
7657,7731c16669,16696
< "13690","acute gonococcal cystitis","icd9cm","098.11"
< "13690","acute gonococcal cystitis","umls","C0153191"
< "13690","acute gonococcal cystitis","mondo","0001777"
< "13691","dermoid cyst of skin","umls","C0349502"
< "13691","dermoid cyst of skin","mondo","0001778"
< "0110096","short-rib thoracic dysplasia 14 with polydactyly","icd10cm","Q04.3"
< "0110096","short-rib thoracic dysplasia 14 with polydactyly","mondo","0014688"
< "11201","parathyroid gland disease","icd10cm","E21.5"
< "11201","parathyroid gland disease","icd9cm","252"
< "11201","parathyroid gland disease","icd9cm","252.9"
< "11201","parathyroid gland disease","mesh","D010279"
< "11201","parathyroid gland disease","umls","C0030517"
< "11201","parathyroid gland disease","mondo","0001223"
< "11200","T cell deficiency","umls","C1274233"
< "11200","T cell deficiency","umls","C1333147"
< "11200","T cell deficiency","mondo","0001222"
< "3443","mammary Paget's disease","umls","C1368019"
< "3443","mammary Paget's disease","mondo","0002648"
< "0111144","preterm premature rupture of the membranes","mondo","0012511"
< "0110795","hereditary spastic paraplegia 43","icd10cm","G11.4"
< "0110795","hereditary spastic paraplegia 43","mondo","0014024"
< "268","liver angiosarcoma","icd10cm","C22.3"
< "268","liver angiosarcoma","umls","C0345907"
< "268","liver angiosarcoma","mondo","0002387"
< "12506","Bell's palsy","icd10cm","G51.0"
< "12506","Bell's palsy","icd9cm","351.0"
< "12506","Bell's palsy","mesh","D020330"
< "12506","Bell's palsy","umls","C0376175"
< "12506","Bell's palsy","mondo","0005665"
< "0110974","brachydactyly type A1B","mondo","0011757"
< "13867","focal labyrinthitis","icd9cm","386.32"
< "13867","focal labyrinthitis","umls","C0155505"
< "13867","focal labyrinthitis","mondo","0001820"
< "0110796","hereditary spastic paraplegia 44","icd10cm","G11.4"
< "0110796","hereditary spastic paraplegia 44","mondo","0013179"
< "7430","childhood germ cell brain tumor","umls","C1377598"
< "7430","childhood germ cell brain tumor","mondo","0004218"
< "5688","Werner syndrome","mesh","D014898"
< "5688","Werner syndrome","umls","C0043119"
< "5688","Werner syndrome","mondo","0010196"
< "2752","glycogen storage disease II","icd10cm","E74.02"
< "2752","glycogen storage disease II","mesh","D006009"
< "2752","glycogen storage disease II","umls","C0017921"
< "2752","glycogen storage disease II","mondo","0009290"
< "5681","ovarian embryonal carcinoma","umls","C0346183"
< "5681","ovarian embryonal carcinoma","mondo","0003581"
< "5680","embryonal testis carcinoma","umls","C0238448"
< "5680","embryonal testis carcinoma","mondo","0006446"
< "5683","hereditary breast ovarian cancer syndrome","mesh","D061325"
< "5683","hereditary breast ovarian cancer syndrome","umls","C0677776"
< "5683","hereditary breast ovarian cancer syndrome","mondo","0003582"
< "2021","placenta cancer","icd10cm","C58"
< "2021","placenta cancer","icd9cm","181"
< "2021","placenta cancer","umls","C0153572"
< "2021","placenta cancer","mondo","0002178"
< "14384","parietal lobe neoplasm","icd10cm","C71.3"
< "14384","parietal lobe neoplasm","icd9cm","191.3"
< "14384","parietal lobe neoplasm","umls","C0153637"
< "14384","parietal lobe neoplasm","umls","C1263888"
< "14384","parietal lobe neoplasm","mondo","0001952"
< "0080148","T-cell childhood lymphoblastic lymphoma","mondo","0000874"
< "6211","mixed epithelial tumor of ovary","umls","C0346166"
< "6211","mixed epithelial tumor of ovary","mondo","0003811"
< "0080143","congenital fibrosis of the extraocular muscles","mondo","0007614"
< "0080144","childhood acute lymphocytic leukemia","mondo","0000870"
< "0060765","autosomal dominant Robinow syndrome 2","mondo","0014591"
< "6676","Froelich syndrome","icd10cm","E23.6"
< "6676","Froelich syndrome","mesh","D007027"
< "6676","Froelich syndrome","umls","C0016724"
< "6676","Froelich syndrome","mondo","0003962"
< "0111142","oligomeganephronia","icd10cm","Q60.4"
< "0111142","oligomeganephronia","mondo","0016407"
< "6678","tooth and nail syndrome","mesh","C536736"
< "6678","tooth and nail syndrome","umls","C0406735"
< "6678","tooth and nail syndrome","mondo","0008582"
---
> "3946","pituitary-dependent Cushing's disease","icd10cm","E24.0"
> "3946","pituitary-dependent Cushing's disease","mesh","D047748"
> "3946","pituitary-dependent Cushing's disease","umls","C0221406"
> "3946","pituitary-dependent Cushing's disease","mondo","0020528"
> "3947","adrenal gland hyperfunction","mesh","D000308"
> "3947","adrenal gland hyperfunction","umls","C0001622"
> "3947","adrenal gland hyperfunction","mondo","0006640"
> "6700","gastric fundus carcinoma","umls","C0345799"
> "6700","gastric fundus carcinoma","mondo","0003970"
> "6703","gastric pylorus carcinoma","umls","C1333787"
> "6703","gastric pylorus carcinoma","mondo","0003971"
> "6705","gastric body carcinoma","umls","C0345804"
> "6705","gastric body carcinoma","mondo","0003972"
> "6707","malignant triton tumor","umls","C0334616"
> "6707","malignant triton tumor","mondo","0016757"
> "6706","tubular variant testicular seminoma","umls","C1515294"
> "6706","tubular variant testicular seminoma","mondo","0003973"
> "9911","infected hydrocele","icd10cm","N43.1"
> "9911","infected hydrocele","icd9cm","603.1"
> "9911","infected hydrocele","umls","C0156300"
> "9911","infected hydrocele","mondo","0004919"
> "9910","central corneal ulcer","icd10cm","H16.01"
> "9910","central corneal ulcer","icd9cm","370.03"
> "9910","central corneal ulcer","umls","C0155069"
> "9910","central corneal ulcer","mondo","0004918"
> "12072","pylorospasm","icd9cm","537.81"
> "12072","pylorospasm","umls","C0152163"
> "12072","pylorospasm","mondo","0001428"
7733a16699,16700
> "4055","ectomesenchymoma","umls","C0431111"
> "4055","ectomesenchymoma","mondo","0002855"
7739a16707,16710
> "4051","alveolar rhabdomyosarcoma","mesh","D018232"
> "4051","alveolar rhabdomyosarcoma","umls","C0206655"
> "4051","alveolar rhabdomyosarcoma","umls","C0279613"
> "4051","alveolar rhabdomyosarcoma","mondo","0009994"
7742,7744d16712
< "0050616","malignant Leydig cell tumor","umls","C0334410"
< "0050616","malignant Leydig cell tumor","mondo","0000377"
< "0110799","hereditary spastic paraplegia 47","mondo","0013551"
7749,7772c16717,16724
< "9840","esotropia","icd10cm","H50.0"
< "9840","esotropia","icd10cm","H50.00"
< "9840","esotropia","icd9cm","378.0"
< "9840","esotropia","icd9cm","378.00"
< "9840","esotropia","mesh","D004948"
< "9840","esotropia","umls","C0014877"
< "9840","esotropia","mondo","0004896"
< "0110652","long QT syndrome 11","icd10cm","I45.8"
< "0110652","long QT syndrome 11","mondo","0012738"
< "5973","kidney pelvis papillary carcinoma","umls","C1377909"
< "5973","kidney pelvis papillary carcinoma","mondo","0003716"
< "8283","peritonitis","icd9cm","567.8"
< "8283","peritonitis","icd9cm","567.89"
< "8283","peritonitis","mesh","D010538"
< "8283","peritonitis","umls","C0029823"
< "8283","peritonitis","mondo","0004522"
< "3610","breast mucinous carcinoma","umls","C1334807"
< "3610","breast mucinous carcinoma","mondo","0002707"
< "14798","Blount's disease","mesh","C536237"
< "14798","Blount's disease","umls","C0220757"
< "14798","Blount's disease","mondo","0017194"
< "0050448","hereditary mucosal leukokeratosis","mesh","D053529"
< "0050448","hereditary mucosal leukokeratosis","umls","C1721005"
< "0050448","hereditary mucosal leukokeratosis","mondo","0015748"
---
> "0080036","SOST-related sclerosing bone dysplasia","mondo","0009395"
> "3611","acute retinal necrosis syndrome","mesh","D015882"
> "3611","acute retinal necrosis syndrome","umls","C0035319"
> "3611","acute retinal necrosis syndrome","mondo","0006638"
> "3612","retinitis","icd10cm","H30.9"
> "3612","retinitis","mesh","D012173"
> "3612","retinitis","umls","C0035333"
> "3612","retinitis","mondo","0002708"
7782,7788c16734,16743
< "3819","toxicodendron dermatitis","mesh","D011040"
< "3819","toxicodendron dermatitis","umls","C0032342"
< "3819","toxicodendron dermatitis","mondo","0006616"
< "882","heterophyiasis","icd10cm","B66.8"
< "882","heterophyiasis","icd9cm","121.6"
< "882","heterophyiasis","umls","C0152071"
< "882","heterophyiasis","mondo","0004662"
---
> "3615","infiltrating angiolipoma","umls","C1305256"
> "3615","infiltrating angiolipoma","mondo","0002710"
> "3616","angiolipoma","mesh","D018206"
> "3616","angiolipoma","umls","C0206632"
> "3616","angiolipoma","mondo","0006085"
> "3617","epidural spinal canal angiolipoma","umls","C1333416"
> "3617","epidural spinal canal angiolipoma","mondo","0002712"
> "3618","epidural neoplasm","mesh","D015174"
> "3618","epidural neoplasm","umls","C0014536"
> "3618","epidural neoplasm","mondo","0002713"
7802,7812d16756
< "2297","leptospirosis","icd10cm","A27"
< "2297","leptospirosis","icd10cm","A27.0"
< "2297","leptospirosis","icd10cm","A27.9"
< "2297","leptospirosis","icd9cm","100"
< "2297","leptospirosis","icd9cm","100.0"
< "2297","leptospirosis","icd9cm","100.9"
< "2297","leptospirosis","mesh","D007922"
< "2297","leptospirosis","mesh","D014895"
< "2297","leptospirosis","umls","C0023364"
< "2297","leptospirosis","umls","C0043102"
< "2297","leptospirosis","mondo","0005825"
7823,7827c16767,16776
< "10273","heart conduction disease","icd9cm","426.6"
< "10273","heart conduction disease","umls","C0029630"
< "10273","heart conduction disease","mondo","0000992"
< "6938","pediatric intraocular retinoblastoma","umls","C1321869"
< "6938","pediatric intraocular retinoblastoma","mondo","0004045"
---
> "2569","retinal drusen","icd9cm","362.57"
> "2569","retinal drusen","mesh","D015593"
> "2569","retinal drusen","umls","C0035312"
> "2569","retinal drusen","mondo","0006949"
> "2568","cervicitis","icd10cm","N72"
> "2568","cervicitis","icd9cm","616.0"
> "2568","cervicitis","mesh","D002575"
> "2568","cervicitis","umls","C0007860"
> "2568","cervicitis","umls","C0007861"
> "2568","cervicitis","mondo","0002345"
7830,7841c16779
< "13241","Behcet's disease","icd10cm","M35.2"
< "13241","Behcet's disease","icd9cm","136.1"
< "13241","Behcet's disease","mesh","D001528"
< "13241","Behcet's disease","umls","C0004943"
< "13241","Behcet's disease","mondo","0007191"
< "0110072","arrhythmogenic right ventricular dysplasia 3","icd10cm","I42.8"
< "0110072","arrhythmogenic right ventricular dysplasia 3","mondo","0011188"
< "288","endometriosis of uterus","icd10cm","N80.0"
< "288","endometriosis of uterus","icd9cm","617.0"
< "288","endometriosis of uterus","mesh","D062788"
< "288","endometriosis of uterus","umls","C0341858"
< "288","endometriosis of uterus","mondo","0010888"
---
> "0111139","mitochondrial complex III deficiency","mondo","0015448"
7848,7855c16786,16789
< "0090063","familial cold autoinflammatory syndrome 2","mesh","C567090"
< "0090063","familial cold autoinflammatory syndrome 2","umls","C2673198"
< "0090063","familial cold autoinflammatory syndrome 2","mondo","0012724"
< "2565","macular corneal dystrophy","icd10cm","H18.55"
< "2565","macular corneal dystrophy","icd9cm","371.55"
< "2565","macular corneal dystrophy","mesh","D003317"
< "2565","macular corneal dystrophy","umls","C0024439"
< "2565","macular corneal dystrophy","mondo","0009020"
---
> "0111131","focal segmental glomerulosclerosis 6","icd10cm","N04.1"
> "0111131","focal segmental glomerulosclerosis 6","mondo","0013589"
> "0111136","congenital generalized lipodystrophy type 2","icd10cm","E88.1"
> "0111136","congenital generalized lipodystrophy type 2","mondo","0010020"
7862,7882c16796,16803
< "10914","amnestic disorder","icd10cm","R41.3"
< "10914","amnestic disorder","icd9cm","294.0"
< "10914","amnestic disorder","mesh","D000647"
< "10914","amnestic disorder","umls","C0002622"
< "10914","amnestic disorder","umls","C0002625"
< "10914","amnestic disorder","mondo","0001152"
< "10915","Wernicke-Korsakoff syndrome","mesh","D020915"
< "10915","Wernicke-Korsakoff syndrome","umls","C0349464"
< "10915","Wernicke-Korsakoff syndrome","mondo","0010198"
< "0110372","retinitis pigmentosa 4","icd10cm","H35.5"
< "0110372","retinitis pigmentosa 4","mondo","0013395"
< "2365","West Nile encephalitis","icd10cm","A92.31"
< "2365","West Nile encephalitis","icd9cm","066.41"
< "2365","West Nile encephalitis","mesh","D014901"
< "2365","West Nile encephalitis","umls","C0751583"
< "2365","West Nile encephalitis","mondo","0019376"
< "2364","post-thrombotic syndrome","icd10cm","I87.0"
< "2364","post-thrombotic syndrome","icd9cm","459.1"
< "2364","post-thrombotic syndrome","mesh","D011186"
< "2364","post-thrombotic syndrome","umls","C0032807"
< "2364","post-thrombotic syndrome","mondo","0005928"
---
> "11429","endometriosis of pelvic peritoneum","icd10cm","N80.3"
> "11429","endometriosis of pelvic peritoneum","icd9cm","617.3"
> "11429","endometriosis of pelvic peritoneum","umls","C0156345"
> "11429","endometriosis of pelvic peritoneum","mondo","0001285"
> "11428","endometriosis of intestine","icd10cm","N80.5"
> "11428","endometriosis of intestine","icd9cm","617.5"
> "11428","endometriosis of intestine","umls","C0156347"
> "11428","endometriosis of intestine","mondo","0001284"
7887,7917c16808,16813
< "0050536","SC phocomelia syndrome","mondo","0010009"
< "9132","liver carcinoma in situ","icd10cm","D01.5"
< "9132","liver carcinoma in situ","icd9cm","230.8"
< "9132","liver carcinoma in situ","umls","C0496854"
< "9132","liver carcinoma in situ","mondo","0004715"
< "0050534","congenital stationary night blindness","icd10cm","H53.63"
< "0050534","congenital stationary night blindness","icd9cm","368.61"
< "0050534","congenital stationary night blindness","mesh","C537743"
< "0050534","congenital stationary night blindness","umls","C1306122"
< "0050534","congenital stationary night blindness","mondo","0016293"
< "0070173","spermatogenic failure 7","mondo","0013070"
< "0070174","spermatogenic failure 17","mondo","0014970"
< "4795","GM2 gangliosidosis, AB variant","mesh","D049290"
< "4795","GM2 gangliosidosis, AB variant","umls","C0268275"
< "4795","GM2 gangliosidosis, AB variant","mondo","0010099"
< "0070176","spermatogenic failure 4","mondo","0010052"
< "2580","rhizomelic chondrodysplasia punctata","icd10cm","E71.540"
< "2580","rhizomelic chondrodysplasia punctata","mesh","D018902"
< "2580","rhizomelic chondrodysplasia punctata","umls","C0282529"
< "2580","rhizomelic chondrodysplasia punctata","mondo","0015776"
< "0070178","spermatogenic failure 10","mondo","0013901"
< "0070179","spermatogenic failure 14","mondo","0014366"
< "1612","breast cancer","icd10cm","C50"
< "1612","breast cancer","icd10cm","C50-C50"
< "1612","breast cancer","mesh","D001943"
< "1612","breast cancer","umls","C0006142"
< "1612","breast cancer","mondo","0007254"
< "0050538","Charcot-Marie-Tooth disease type 1","mondo","0019011"
< "0050539","Charcot-Marie-Tooth disease type 2","icd9cm","356.0"
< "0050539","Charcot-Marie-Tooth disease type 2","umls","C0392553"
< "0050539","Charcot-Marie-Tooth disease type 2","mondo","0018993"
---
> "11427","endosalpingiosis","umls","C0269106"
> "11427","endosalpingiosis","mondo","0001283"
> "5022","aflatoxins-related hepatocellular carcinoma","umls","C1332222"
> "5022","aflatoxins-related hepatocellular carcinoma","mondo","0003245"
> "5026","sclerosing hepatic carcinoma","umls","C1266018"
> "5026","sclerosing hepatic carcinoma","mondo","0003246"
7921,7928c16817,16842
< "1862","jaw cancer","mesh","D007573"
< "1862","jaw cancer","umls","C0022364"
< "1862","jaw cancer","mondo","0002131"
< "13359","Ehlers-Danlos syndrome","icd10cm","Q79.6"
< "13359","Ehlers-Danlos syndrome","icd9cm","756.83"
< "13359","Ehlers-Danlos syndrome","mesh","D004535"
< "13359","Ehlers-Danlos syndrome","umls","C0013720"
< "13359","Ehlers-Danlos syndrome","mondo","0020066"
---
> "4441","dysgerminoma","mesh","D004407"
> "4441","dysgerminoma","umls","C0013377"
> "4441","dysgerminoma","mondo","0003002"
> "4442","cervical alveolar soft part sarcoma","umls","C1516408"
> "4442","cervical alveolar soft part sarcoma","mondo","0003003"
> "13352","ego-dystonic sexual orientation","icd9cm","302.0"
> "13352","ego-dystonic sexual orientation","umls","C0233880"
> "13352","ego-dystonic sexual orientation","mondo","0001693"
> "0111392","mucopolysaccharidosis type IVB","icd10cm","E76.211"
> "0111392","mucopolysaccharidosis type IVB","umls","C0086652"
> "0111393","mucopolysaccharidosis type IIIC","umls","C0086649"
> "13357","chondromalacia patellae","icd10cm","M22.4"
> "13357","chondromalacia patellae","icd9cm","717.7"
> "13357","chondromalacia patellae","mesh","D046789"
> "13357","chondromalacia patellae","umls","C0008475"
> "13357","chondromalacia patellae","mondo","0008207"
> "4447","cystoid macular edema","mesh","D008269"
> "4447","cystoid macular edema","umls","C0024440"
> "4447","cystoid macular edema","mondo","0007935"
> "4448","macular degeneration","umls","C0024437"
> "4448","macular degeneration","mondo","0003004"
> "4449","macular retinal edema","mesh","D008269"
> "4449","macular retinal edema","umls","C0271051"
> "4449","macular retinal edema","mondo","0003005"
> "0111398","congenital dyserythropoietic anemia type Ia","umls","C3810185"
> "0111399","congenital dyserythropoietic anemia type III","umls","C0271934"
7932,7933c16846,16847
< "4932","ampulla of Vater carcinoma","umls","C0262401"
< "4932","ampulla of Vater carcinoma","mondo","0017590"
---
> "0090116","spondylocarpotarsal synostosis syndrome","icd10cm","Q76.4"
> "0090116","spondylocarpotarsal synostosis syndrome","mondo","0010094"
7937,8028c16851,16876
< "0110719","Warburg micro syndrome 4","icd10cm","Q87.0"
< "0110719","Warburg micro syndrome 4","mondo","0014296"
< "0110718","Warburg micro syndrome 3","icd10cm","Q87.0"
< "0110718","Warburg micro syndrome 3","mondo","0013638"
< "4680","breast metaplastic carcinoma","umls","C1334708"
< "4680","breast metaplastic carcinoma","mondo","0006043"
< "0090113","RIDDLE syndrome","icd10cm","D82.8"
< "0090113","RIDDLE syndrome","mesh","C567453"
< "0090113","RIDDLE syndrome","mondo","0012764"
< "0110715","congenital stationary night blindness autosomal dominant 3","mondo","0012497"
< "0060897","Parkinson's disease 17","mondo","0013625"
< "0110717","Warburg micro syndrome 2","icd10cm","Q87.0"
< "0110717","Warburg micro syndrome 2","mondo","0013641"
< "0060895","autosomal dominant Parkinson's disease 4","icd10cm","G20"
< "0060895","autosomal dominant Parkinson's disease 4","mondo","0011562"
< "0110863","congenital stationary night blindness autosomal dominant 2","mondo","0008099"
< "0110710","hypotrichosis 13","mondo","0014390"
< "0060890","ectopic Cushing syndrome","icd10cm","E24.3"
< "0060890","ectopic Cushing syndrome","mondo","0020527"
< "0110860","polycystic kidney disease 3","mondo","0010916"
< "0050800","creatine transporter deficiency","mondo","0010305"
< "2101","vulva squamous cell carcinoma","umls","C0280856"
< "2101","vulva squamous cell carcinoma","mondo","0024609"
< "2106","myotonia congenita","icd9cm","359.22"
< "2106","myotonia congenita","mesh","D009224"
< "2106","myotonia congenita","umls","C0027127"
< "2106","myotonia congenita","mondo","0009710"
< "6053","pediatric germ cell cancer","umls","C0279014"
< "6053","pediatric germ cell cancer","mondo","0003751"
< "5117","dermoid cyst of ovary","mesh","C562731"
< "5117","dermoid cyst of ovary","umls","C0237020"
< "5117","dermoid cyst of ovary","mondo","0008167"
< "2639","breast pericanalicular fibroadenoma","umls","C0334497"
< "2639","breast pericanalicular fibroadenoma","mondo","0002371"
< "5112","copper deficiency myelopathy","mesh","D013540"
< "5112","copper deficiency myelopathy","umls","C0038981"
< "5112","copper deficiency myelopathy","mondo","0003280"
< "2634","cystadenoma","mesh","D003537"
< "2634","cystadenoma","umls","C0010633"
< "2634","cystadenoma","mondo","0002369"
< "0050535","exudative vitreoretinopathy","icd10cm","H35.00"
< "0050535","exudative vitreoretinopathy","icd9cm","362.10"
< "0050535","exudative vitreoretinopathy","umls","C0004608"
< "0050535","exudative vitreoretinopathy","mondo","0019516"
< "2636","ovarian Brenner tumor","mesh","D001948"
< "2636","ovarian Brenner tumor","umls","C0006160"
< "2636","ovarian Brenner tumor","mondo","0002370"
< "2632","papillary serous adenocarcinoma","umls","C0334359"
< "2632","papillary serous adenocarcinoma","umls","C0334361"
< "2632","papillary serous adenocarcinoma","mondo","0002368"
< "2986","IgA glomerulonephritis","mesh","D005922"
< "2986","IgA glomerulonephritis","umls","C0017661"
< "2986","IgA glomerulonephritis","mondo","0005342"
< "0050156","idiopathic pulmonary fibrosis","icd10cm","J84.112"
< "0050156","idiopathic pulmonary fibrosis","icd9cm","516.31"
< "0050156","idiopathic pulmonary fibrosis","mesh","D054990"
< "0050156","idiopathic pulmonary fibrosis","umls","C1800706"
< "0050156","idiopathic pulmonary fibrosis","mondo","0008345"
< "0050157","cryptogenic organizing pneumonia","icd10cm","J84.116"
< "0050157","cryptogenic organizing pneumonia","icd9cm","516.36"
< "0050157","cryptogenic organizing pneumonia","mesh","D018549"
< "0050157","cryptogenic organizing pneumonia","umls","C0242770"
< "0050157","cryptogenic organizing pneumonia","mondo","0015264"
< "5403","microcystic adenoma","mesh","D000236"
< "5403","microcystic adenoma","umls","C0205648"
< "5403","microcystic adenoma","mondo","0003435"
< "0070039","autosomal dominant non-syndromic intellectual disability 9","mondo","0013656"
< "9597","Krukenberg carcinoma","mesh","D007725"
< "9597","Krukenberg carcinoma","umls","C0022790"
< "9597","Krukenberg carcinoma","mondo","0004829"
< "0050158","desquamative interstitial pneumonia","icd10cm","J84.115"
< "0050158","desquamative interstitial pneumonia","icd10cm","J84.117"
< "0050158","desquamative interstitial pneumonia","icd9cm","516.34"
< "0050158","desquamative interstitial pneumonia","icd9cm","516.37"
< "0050158","desquamative interstitial pneumonia","mesh","C562470"
< "0050158","desquamative interstitial pneumonia","umls","C0238378"
< "0050158","desquamative interstitial pneumonia","mondo","0009887"
< "0070038","autosomal dominant non-syndromic intellectual disability 8","mondo","0013655"
< "2121","ectodermal dysplasia","mondo","0019287"
< "874","bacterial pneumonia","icd10cm","J15.9"
< "874","bacterial pneumonia","icd9cm","482.9"
< "874","bacterial pneumonia","mesh","D018410"
< "874","bacterial pneumonia","umls","C0004626"
< "874","bacterial pneumonia","mondo","0004652"
< "873","anaerobic pneumonia","icd9cm","482.81"
< "873","anaerobic pneumonia","umls","C0375327"
< "873","anaerobic pneumonia","mondo","0004649"
< "1521","cecum cancer","icd10cm","C18.0"
< "1521","cecum cancer","icd9cm","153.4"
< "1521","cecum cancer","mesh","D002430"
< "1521","cecum cancer","umls","C0153437"
< "1521","cecum cancer","mondo","0002033"
---
> "960","esophagus leiomyoma","umls","C0238114"
> "960","esophagus leiomyoma","mondo","0004832"
> "961","neurofibroma of the esophagus","umls","C1333463"
> "961","neurofibroma of the esophagus","mondo","0004837"
> "962","neurofibroma","mesh","D009455"
> "962","neurofibroma","umls","C0027830"
> "962","neurofibroma","mondo","0016755"
> "963","episodic ataxia","mesh","C580065"
> "963","episodic ataxia","umls","C1720189"
> "963","episodic ataxia","mondo","0016227"
> "0090118","congenital amegakaryocytic thrombocytopenia","mesh","C535982"
> "0090118","congenital amegakaryocytic thrombocytopenia","umls","C1327915"
> "0090118","congenital amegakaryocytic thrombocytopenia","mondo","0011469"
> "0090119","ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","mesh","C535289"
> "0090119","ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","umls","C1785148"
> "0090119","ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","mondo","0007124"
> "14253","retinal dystrophy in systemic or cerebroretinal lipidoses","icd9cm","362.71"
> "14253","retinal dystrophy in systemic or cerebroretinal lipidoses","umls","C0154861"
> "14253","retinal dystrophy in systemic or cerebroretinal lipidoses","mondo","0001925"
> "640","encephalomyelitis","mesh","D004679"
> "640","encephalomyelitis","umls","C0014070"
> "640","encephalomyelitis","mondo","0005156"
> "1243","labia minora cancer","icd10cm","C51.1"
> "1243","labia minora cancer","icd9cm","184.2"
> "1243","labia minora cancer","umls","C0496815"
> "1243","labia minora cancer","mondo","0001526"
8031,8045c16879,16886
< "2747","glycogen storage disease","icd10cm","E74.0"
< "2747","glycogen storage disease","icd10cm","E74.00"
< "2747","glycogen storage disease","icd9cm","271.0"
< "2747","glycogen storage disease","mesh","D006008"
< "2747","glycogen storage disease","umls","C0017919"
< "2747","glycogen storage disease","mondo","0002412"
< "2030","anxiety disorder","icd10cm","F41.9"
< "2030","anxiety disorder","mesh","D001008"
< "2030","anxiety disorder","umls","C0003469"
< "2030","anxiety disorder","mondo","0005618"
< "2749","glycogen storage disease I","icd10cm","E74.01"
< "2749","glycogen storage disease I","mesh","D005953"
< "2749","glycogen storage disease I","umls","C0017920"
< "2749","glycogen storage disease I","mondo","0002413"
< "0110660","congenital myasthenic syndrome 12","mondo","0012518"
---
> "0110661","congenital myasthenic syndrome 20","mondo","0014939"
> "1245","vulva cancer","icd10cm","C51"
> "1245","vulva cancer","icd10cm","C51.9"
> "1245","vulva cancer","icd9cm","184.4"
> "1245","vulva cancer","mesh","D014846"
> "1245","vulva cancer","umls","C0042995"
> "1245","vulva cancer","umls","C0375071"
> "1245","vulva cancer","mondo","0001528"
8048c16889
< "0110665","congenital myasthenic syndrome 3B","mondo","0014584"
---
> "0060828","X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome","mondo","0010473"
8051,8083c16892,16900
< "10487","Hirschsprung's disease","icd10cm","Q43.1"
< "10487","Hirschsprung's disease","mesh","D006627"
< "10487","Hirschsprung's disease","umls","C0019569"
< "10487","Hirschsprung's disease","mondo","0018309"
< "0110041","Alzheimer's disease 8","icd10cm","G30"
< "0110041","Alzheimer's disease 8","mondo","0011777"
< "0110040","Alzheimer's disease 4","mondo","0011743"
< "0110043","Alzheimer's disease 10","icd10cm","G30"
< "0110043","Alzheimer's disease 10","mondo","0012321"
< "0110042","Alzheimer's disease 3","mondo","0011913"
< "0110045","Alzheimer's disease 12","icd10cm","G30"
< "0110045","Alzheimer's disease 12","mondo","0012609"
< "0110044","Alzheimer's disease 11","icd10cm","G30"
< "0110044","Alzheimer's disease 11","mondo","0012344"
< "0110047","Alzheimer's disease 14","icd10cm","G30"
< "0110047","Alzheimer's disease 14","mondo","0012631"
< "0110046","Alzheimer's disease 13","icd10cm","G30"
< "0110046","Alzheimer's disease 13","mondo","0012630"
< "0110049","Alzheimer's disease 17","mondo","0014036"
< "0110048","Alzheimer's disease 15","icd10cm","G30"
< "0110048","Alzheimer's disease 15","mondo","0012632"
< "646","viral encephalitis","mesh","D004671"
< "646","viral encephalitis","umls","C0014055"
< "646","viral encephalitis","mondo","0006009"
< "0080126","mitochondrial DNA depletion syndrome 7","mesh","C535523"
< "0080126","mitochondrial DNA depletion syndrome 7","mondo","0010060"
< "0040003","benzylpenicillin allergy","umls","C0571411"
< "0040002","aspirin allergy","umls","C0004058"
< "0040002","aspirin allergy","mondo","0025518"
< "5204","fructose-1,6-bisphosphatase deficiency","icd10cm","E74.19"
< "5204","fructose-1,6-bisphosphatase deficiency","mesh","D015319"
< "5204","fructose-1,6-bisphosphatase deficiency","umls","C0016756"
< "5204","fructose-1,6-bisphosphatase deficiency","mondo","0009251"
---
> "0110666","congenital myasthenic syndrome 3A","mondo","0014583"
> "3095","germ cell and embryonal cancer","mesh","D009373"
> "3095","germ cell and embryonal cancer","umls","C0027658"
> "3095","germ cell and embryonal cancer","mondo","0002510"
> "7326","cranial pseudosarcomatous fasciitis","umls","C1333162"
> "7326","cranial pseudosarcomatous fasciitis","mondo","0004186"
> "7327","pseudosarcomatous fibromatosis","icd10cm","M72.4"
> "7327","pseudosarcomatous fibromatosis","umls","C0410005"
> "7327","pseudosarcomatous fibromatosis","mondo","0004187"
8091,8109c16908,16914
< "0060167","seasonal affective disorder","mesh","D016574"
< "0060167","seasonal affective disorder","mondo","0000694"
< "9043","uterine cervix leukoplakia","icd10cm","N88.0"
< "9043","uterine cervix leukoplakia","icd9cm","622.2"
< "9043","uterine cervix leukoplakia","umls","C0269194"
< "9043","uterine cervix leukoplakia","mondo","0004702"
< "5208","malignant struma ovarii","umls","C0334525"
< "5208","malignant struma ovarii","mondo","0003332"
< "0040009","lidocaine allergy","umls","C0570646"
< "0040008","isoniazide allergy","icd10cm","Z88.1"
< "1969","cerebral palsy","icd10cm","G80"
< "1969","cerebral palsy","icd10cm","G80.9"
< "1969","cerebral palsy","mesh","D002547"
< "1969","cerebral palsy","umls","C0007789"
< "1969","cerebral palsy","mondo","0006497"
< "0110445","dilated cardiomyopathy 1KK","icd10cm","I42.0"
< "0110445","dilated cardiomyopathy 1KK","mondo","0014100"
< "0110444","dilated cardiomyopathy 1X","icd10cm","I42.0"
< "0110444","dilated cardiomyopathy 1X","mondo","0012704"
---
> "10461","dentin caries","icd10cm","K02"
> "10461","dentin caries","icd9cm","521.02"
> "10461","dentin caries","umls","C0266846"
> "10461","dentin caries","mondo","0001041"
> "7320","ovarian serous cystadenofibroma","umls","C0877572"
> "7320","ovarian serous cystadenofibroma","mondo","0004185"
> "0070318","dry beriberi","icd10cm","E51.11"
8114,8117c16919,16926
< "3540","choroid plexus cancer","mesh","D016545"
< "3540","choroid plexus cancer","umls","C0085138"
< "3540","choroid plexus cancer","mondo","0002681"
< "0110440","dilated cardiomyopathy 1J","mondo","0011541"
---
> "0110441","dilated cardiomyopathy 2B","icd10cm","I42.0"
> "0110441","dilated cardiomyopathy 2B","mondo","0013848"
> "3234","central nervous system lymphoma","icd9cm","200.5"
> "3234","central nervous system lymphoma","umls","C0280803"
> "3234","central nervous system lymphoma","umls","C0742472"
> "3234","central nervous system lymphoma","mondo","0002571"
> "0110443","dilated cardiomyopathy 1B","icd10cm","I42.0"
> "0110443","dilated cardiomyopathy 1B","mondo","0010951"
8121,8122c16930
< "0110448","dilated cardiomyopathy 1HH","icd10cm","I42.0"
< "0110448","dilated cardiomyopathy 1HH","mondo","0013479"
---
> "0070315","hypoplastic right heart syndrome","mondo","0020291"
8123a16932
> "0070317","wet beriberi","icd10cm","E51.12"
8128,8305c16937,16999
< "1616","benign eccrine breast spiradenoma","umls","C1332492"
< "1616","benign eccrine breast spiradenoma","mondo","0002055"
< "0110820","hereditary spastic paraplegia 75","icd10cm","G11.4"
< "0110820","hereditary spastic paraplegia 75","mondo","0014729"
< "0050778","Meckel syndrome","icd9cm","753.1"
< "0050778","Meckel syndrome","icd9cm","753.10"
< "0050778","Meckel syndrome","umls","C0311245"
< "0050778","Meckel syndrome","mondo","0018921"
< "13417","alexia","icd9cm","315.01"
< "13417","alexia","mesh","D004410"
< "13417","alexia","mesh","D004411"
< "13417","alexia","umls","C0002018"
< "13417","alexia","umls","C0013388"
< "13417","alexia","mondo","0001712"
< "1788","peritoneal mesothelioma","icd10cm","C45.1"
< "1788","peritoneal mesothelioma","umls","C0346109"
< "1788","peritoneal mesothelioma","umls","C0854886"
< "1788","peritoneal mesothelioma","mondo","0005512"
< "768","retinoblastoma","mesh","D012175"
< "768","retinoblastoma","umls","C0035335"
< "768","retinoblastoma","mondo","0008380"
< "265","spleen angiosarcoma","umls","C0346424"
< "265","spleen angiosarcoma","mondo","0002376"
< "11197","serous conjunctivitis except viral","icd10cm","H10.23"
< "11197","serous conjunctivitis except viral","icd9cm","372.01"
< "11197","serous conjunctivitis except viral","umls","C0155142"
< "11197","serous conjunctivitis except viral","mondo","0001219"
< "2962","Cockayne syndrome","icd10cm","Q87.1"
< "2962","Cockayne syndrome","mesh","D003057"
< "2962","Cockayne syndrome","umls","C0009207"
< "2962","Cockayne syndrome","mondo","0016006"
< "11198","DiGeorge syndrome","icd10cm","D82.1"
< "11198","DiGeorge syndrome","icd9cm","279.11"
< "11198","DiGeorge syndrome","mesh","D004062"
< "11198","DiGeorge syndrome","umls","C0012236"
< "11198","DiGeorge syndrome","mondo","0008564"
< "264","hemangiopericytoma","mesh","D006393"
< "264","hemangiopericytoma","umls","C0018922"
< "264","hemangiopericytoma","mondo","0005094"
< "1785","pituitary cancer","icd10cm","C75.1"
< "1785","pituitary cancer","mesh","D010911"
< "1785","pituitary cancer","umls","C0032019"
< "1785","pituitary cancer","umls","C0496842"
< "1785","pituitary cancer","mondo","0002109"
< "3049","Churg-Strauss syndrome","icd10cm","M30.1"
< "3049","Churg-Strauss syndrome","mesh","D015267"
< "3049","Churg-Strauss syndrome","umls","C0008728"
< "3049","Churg-Strauss syndrome","mondo","0015943"
< "0050831","familial encephalopathy with neuroserpin inclusion bodies","mesh","C536841"
< "0050831","familial encephalopathy with neuroserpin inclusion bodies","mondo","0011412"
< "0050835","generalized dystonia","icd10cm","G24.1"
< "0050835","generalized dystonia","icd10cm","G24.2"
< "0050835","generalized dystonia","icd9cm","333.6"
< "0050835","generalized dystonia","icd9cm","333.8"
< "0050835","generalized dystonia","mesh","D004422"
< "0050835","generalized dystonia","mesh","D020821"
< "0050835","generalized dystonia","umls","C0013423"
< "0050835","generalized dystonia","umls","C0154674"
< "0050835","generalized dystonia","umls","C0154675"
< "0050835","generalized dystonia","umls","C0393598"
< "0050835","generalized dystonia","umls","C0393601"
< "0050835","generalized dystonia","umls","C0752207"
< "0050835","generalized dystonia","mondo","0000476"
< "0050834","CHARGE syndrome","mesh","D058747"
< "0050834","CHARGE syndrome","umls","C0265354"
< "0050834","CHARGE syndrome","umls","C2936502"
< "0050834","CHARGE syndrome","mondo","0008965"
< "0110389","retinitis pigmentosa 73","icd10cm","H35.5"
< "0110389","retinitis pigmentosa 73","mondo","0014687"
< "6873","skin tag","umls","C0037293"
< "6873","skin tag","mondo","0004026"
< "3044","food allergy","mesh","D005512"
< "3044","food allergy","umls","C0016470"
< "3044","food allergy","mondo","0002497"
< "3047","Wissler's syndrome","mesh","D014924"
< "3047","Wissler's syndrome","umls","C0043195"
< "3047","Wissler's syndrome","mondo","0006018"
< "338","cranial nerve neoplasm","mesh","D003390"
< "338","cranial nerve neoplasm","umls","C0010267"
< "338","cranial nerve neoplasm","mondo","0002633"
< "0110478","autosomal recessive nonsyndromic deafness 20","icd10cm","H90.3"
< "0110478","autosomal recessive nonsyndromic deafness 20","mondo","0011392"
< "0110828","Usher syndrome type 3","mesh","D052245"
< "0110828","Usher syndrome type 3","umls","C1568248"
< "0110828","Usher syndrome type 3","mondo","0016485"
< "1079","setariasis","mesh","D012719"
< "1079","setariasis","umls","C0036850"
< "1079","setariasis","mondo","0005957"
< "3234","central nervous system lymphoma","icd9cm","200.5"
< "3234","central nervous system lymphoma","umls","C0280803"
< "3234","central nervous system lymphoma","umls","C0742472"
< "3234","central nervous system lymphoma","mondo","0002571"
< "1074","kidney failure","icd10cm","N19"
< "1074","kidney failure","icd9cm","586"
< "1074","kidney failure","mesh","D051437"
< "1074","kidney failure","umls","C0035078"
< "1074","kidney failure","mondo","0001106"
< "0060824","syndromic X-linked intellectual disability Raymond type","icd10cm","Q87.8"
< "0060824","syndromic X-linked intellectual disability Raymond type","mondo","0010427"
< "0110289","autosomal recessive limb-girdle muscular dystrophy type 2Y","icd10cm","G71.0"
< "0110289","autosomal recessive limb-girdle muscular dystrophy type 2Y","mondo","0014900"
< "0110288","autosomal recessive limb-girdle muscular dystrophy type 2W","mondo","0014788"
< "0110287","autosomal recessive limb-girdle muscular dystrophy type 2S","icd10cm","G71.0"
< "0110287","autosomal recessive limb-girdle muscular dystrophy type 2S","mondo","0014144"
< "8923","skin melanoma","icd10cm","C43"
< "8923","skin melanoma","icd10cm","C43.9"
< "8923","skin melanoma","icd9cm","172"
< "8923","skin melanoma","icd9cm","172.9"
< "8923","skin melanoma","mesh","C562393"
< "8923","skin melanoma","umls","C0151779"
< "8923","skin melanoma","mondo","0005012"
< "0110285","autosomal recessive limb-girdle muscular dystrophy type 2Q","icd10cm","G71.0"
< "0110285","autosomal recessive limb-girdle muscular dystrophy type 2Q","mondo","0013390"
< "0110284","autosomal recessive limb-girdle muscular dystrophy type 2L","icd10cm","G71.0"
< "0110284","autosomal recessive limb-girdle muscular dystrophy type 2L","mondo","0012652"
< "0110283","autosomal recessive limb-girdle muscular dystrophy type 2J","icd10cm","G71.0"
< "0110283","autosomal recessive limb-girdle muscular dystrophy type 2J","mondo","0012127"
< "0110282","autosomal recessive limb-girdle muscular dystrophy type 2H","icd10cm","G71.0"
< "0110282","autosomal recessive limb-girdle muscular dystrophy type 2H","mondo","0009683"
< "0110281","autosomal recessive limb-girdle muscular dystrophy type 2G","icd10cm","G71.0"
< "0110281","autosomal recessive limb-girdle muscular dystrophy type 2G","mondo","0011170"
< "0110280","autosomal recessive limb-girdle muscular dystrophy type 2F","icd10cm","G71.0"
< "0110280","autosomal recessive limb-girdle muscular dystrophy type 2F","mondo","0011028"
< "13501","Mobius syndrome","icd10cm","Q87.0"
< "13501","Mobius syndrome","mesh","D020331"
< "13501","Mobius syndrome","umls","C0221060"
< "13501","Mobius syndrome","mondo","0008006"
< "0090011","immunodeficiency-centromeric instability-facial anomalies syndrome 4","icd10cm","D84.8"
< "0090011","immunodeficiency-centromeric instability-facial anomalies syndrome 4","mondo","0014829"
< "0070135","autosomal recessive cutis laxa type IA","icd10cm","Q82.8"
< "0070135","autosomal recessive cutis laxa type IA","mondo","0009052"
< "678","progressive supranuclear palsy","icd10cm","G23.1"
< "678","progressive supranuclear palsy","mesh","D013494"
< "678","progressive supranuclear palsy","umls","C0038868"
< "678","progressive supranuclear palsy","mondo","0019037"
< "0111102","maturity-onset diabetes of the young type 3","mondo","0010894"
< "674","cleft palate","icd10cm","Q35"
< "674","cleft palate","icd10cm","Q35.9"
< "674","cleft palate","icd9cm","749.0"
< "674","cleft palate","icd9cm","749.00"
< "674","cleft palate","mesh","D002972"
< "674","cleft palate","umls","C0008925"
< "674","cleft palate","mondo","0016064"
< "4337","tinea capitis","icd9cm","110.0"
< "4337","tinea capitis","mesh","D014006"
< "4337","tinea capitis","umls","C0011640"
< "4337","tinea capitis","mondo","0002967"
< "676","juvenile rheumatoid arthritis","icd10cm","M08.4"
< "676","juvenile rheumatoid arthritis","icd10cm","M08.40"
< "676","juvenile rheumatoid arthritis","icd9cm","714.3"
< "676","juvenile rheumatoid arthritis","icd9cm","714.31"
< "676","juvenile rheumatoid arthritis","icd9cm","714.32"
< "676","juvenile rheumatoid arthritis","icd9cm","714.33"
< "676","juvenile rheumatoid arthritis","umls","C0157916"
< "676","juvenile rheumatoid arthritis","umls","C0157917"
< "676","juvenile rheumatoid arthritis","umls","C0157918"
< "676","juvenile rheumatoid arthritis","umls","C0409667"
< "676","juvenile rheumatoid arthritis","mondo","0011429"
< "0111101","maturity-onset diabetes of the young type 5","mondo","0007669"
< "672","spleen cancer","icd10cm","C26.1"
< "672","spleen cancer","mesh","D013160"
< "672","spleen cancer","umls","C0037999"
< "672","spleen cancer","umls","C0153470"
< "672","spleen cancer","mondo","0005966"
< "12119","hemosiderosis","mesh","D006486"
< "12119","hemosiderosis","umls","C0019114"
< "12119","hemosiderosis","mondo","0001436"
< "0090012","severe combined immunodeficiency with sensitivity to ionizing radiation","icd10cm","D81.1"
< "0090012","severe combined immunodeficiency with sensitivity to ionizing radiation","mondo","0011225"
< "9220","central sleep apnea","mesh","D020182"
< "9220","central sleep apnea","umls","C0520680"
< "9220","central sleep apnea","mondo","0004731"
< "3133","acute porphyria","mesh","D017094"
< "3133","acute porphyria","umls","C0162533"
< "3133","acute porphyria","mondo","0002520"
< "0111107","maturity-onset diabetes of the young type 9","mondo","0012818"
< "0090014","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive","icd10cm","D81.2"
< "0090014","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive","mondo","0012163"
---
> "8913","dermatophytosis","icd10cm","B35"
> "8913","dermatophytosis","icd10cm","B35.9"
> "8913","dermatophytosis","icd9cm","110"
> "8913","dermatophytosis","icd9cm","110.9"
> "8913","dermatophytosis","umls","C0011636"
> "8913","dermatophytosis","mondo","0004678"
> "1965","fallopian tube leiomyosarcoma","umls","C1517116"
> "1965","fallopian tube leiomyosarcoma","mondo","0002159"
> "11847","coronary thrombosis","icd10cm","I21"
> "11847","coronary thrombosis","icd10cm","I22"
> "11847","coronary thrombosis","mesh","D003328"
> "11847","coronary thrombosis","umls","C0010072"
> "11847","coronary thrombosis","mondo","0006716"
> "11843","coronary artery anomaly","icd9cm","746.85"
> "11843","coronary artery anomaly","umls","C0158623"
> "11843","coronary artery anomaly","mondo","0001389"
> "11840","coronary artery vasospasm","mesh","D003329"
> "11840","coronary artery vasospasm","umls","C0010073"
> "11840","coronary artery vasospasm","mondo","0005356"
> "5196","fallopian tube adenomatoid tumor","umls","C1517110"
> "5196","fallopian tube adenomatoid tumor","mondo","0003328"
> "7328","iris spindle cell melanoma","umls","C1334287"
> "7328","iris spindle cell melanoma","mondo","0004188"
> "10081","syphilitic encephalitis","icd9cm","094.81"
> "10081","syphilitic encephalitis","umls","C0153168"
> "10081","syphilitic encephalitis","mondo","0000937"
> "5193","nodular ganglioneuroblastoma","umls","C1517445"
> "5193","nodular ganglioneuroblastoma","mondo","0003325"
> "1963","fallopian tube carcinoma","mesh","D005185"
> "1963","fallopian tube carcinoma","umls","C0238122"
> "1963","fallopian tube carcinoma","mondo","0006206"
> "1678","chronic interstitial cystitis","icd10cm","N30.1"
> "1678","chronic interstitial cystitis","icd9cm","595.1"
> "1678","chronic interstitial cystitis","mesh","D018856"
> "1678","chronic interstitial cystitis","umls","C0600040"
> "1678","chronic interstitial cystitis","mondo","0018301"
> "1679","cystitis","icd10cm","N30"
> "1679","cystitis","icd10cm","N30.9"
> "1679","cystitis","icd9cm","595"
> "1679","cystitis","icd9cm","595.9"
> "1679","cystitis","mesh","D003556"
> "1679","cystitis","umls","C0010692"
> "1679","cystitis","mondo","0006032"
> "1677","low implantation of placenta","icd9cm","641.0"
> "1677","low implantation of placenta","umls","C0156617"
> "1677","low implantation of placenta","mondo","0002077"
> "1670","Behcet's syndrome arthropathy","icd9cm","711.2"
> "1670","Behcet's syndrome arthropathy","icd9cm","711.20"
> "1670","Behcet's syndrome arthropathy","umls","C0157770"
> "1670","Behcet's syndrome arthropathy","mondo","0002074"
> "1672","spontaneous tension pneumothorax","icd10cm","J93.0"
> "1672","spontaneous tension pneumothorax","icd9cm","512.0"
> "1672","spontaneous tension pneumothorax","umls","C0155907"
> "1672","spontaneous tension pneumothorax","mondo","0002075"
> "1673","pneumothorax","icd10cm","J93.1"
> "1673","pneumothorax","mesh","D011030"
> "1673","pneumothorax","umls","C0029850"
> "1673","pneumothorax","mondo","0002076"
> "2550","tactile epilepsy","umls","C0393724"
> "2550","tactile epilepsy","mondo","0002340"
> "2555","granulomatous angiitis","mesh","D020293"
> "2555","granulomatous angiitis","umls","C0018202"
> "2555","granulomatous angiitis","mondo","0002341"
8309,8408c17003,17040
< "0110113","atrial heart septal defect 8","icd10cm","Q21.1"
< "0110113","atrial heart septal defect 8","mondo","0013750"
< "0060551","poikiloderma with neutropenia","icd10cm","D82.8"
< "0060551","poikiloderma with neutropenia","mesh","C565820"
< "0060551","poikiloderma with neutropenia","mondo","0011405"
< "0111105","maturity-onset diabetes of the young type 8","mondo","0012348"
< "14744","Partington syndrome","mesh","C562446"
< "14744","Partington syndrome","umls","C0220775"
< "14744","Partington syndrome","mondo","0010654"
< "0060559","lethal congenital contracture syndrome 1","mesh","C537194"
< "0060559","lethal congenital contracture syndrome 1","umls","C1854664"
< "0060559","lethal congenital contracture syndrome 1","mondo","0009670"
< "14748","Sotos syndrome","icd10cm","Q87.3"
< "14748","Sotos syndrome","mesh","D058495"
< "14748","Sotos syndrome","umls","C0175695"
< "14748","Sotos syndrome","mondo","0019349"
< "0050619","paranasal sinus cancer","mesh","D010255"
< "0050619","paranasal sinus cancer","umls","C0280334"
< "0050619","paranasal sinus cancer","umls","C0854995"
< "0050619","paranasal sinus cancer","umls","C1335336"
< "0050619","paranasal sinus cancer","umls","C1335337"
< "0050619","paranasal sinus cancer","umls","C1335340"
< "0050619","paranasal sinus cancer","mondo","0000380"
< "5183","hereditary Wilms' tumor","umls","C0677779"
< "5183","hereditary Wilms' tumor","mondo","0003321"
< "0050636","familial visceral amyloidosis","mondo","0007099"
< "6019","central nervous system immature teratoma","umls","C1332883"
< "6019","central nervous system immature teratoma","mondo","0003735"
< "0060391","chromosome 13q14 deletion syndrome","icd10cm","Q93.5"
< "0060391","chromosome 13q14 deletion syndrome","mondo","0013481"
< "0060390","distal 10q deletion syndrome","icd10cm","Q93.5"
< "0060390","distal 10q deletion syndrome","mesh","C567182"
< "0060390","distal 10q deletion syndrome","mondo","0012315"
< "0060393","chromosome 15q11.2 deletion syndrome","mesh","C557830"
< "0060393","chromosome 15q11.2 deletion syndrome","umls","C3180937"
< "0060393","chromosome 15q11.2 deletion syndrome","mondo","0014294"
< "0090018","autosomal dominant familial periodic fever","icd10cm","E85.0"
< "0090018","autosomal dominant familial periodic fever","mondo","0007727"
< "0060779","congenital malabsorptive diarrhea 4","icd10cm","P78.3"
< "0060779","congenital malabsorptive diarrhea 4","mondo","0012479"
< "0060778","congenital diarrhea 7 with exudative enteropathy","icd10cm","P78.3"
< "0060778","congenital diarrhea 7 with exudative enteropathy","mondo","0014375"
< "1325","bronchus cancer","icd10cm","C34"
< "1325","bronchus cancer","icd10cm","C34.9"
< "1325","bronchus cancer","icd9cm","162.9"
< "1325","bronchus cancer","umls","C0348343"
< "1325","bronchus cancer","mondo","0001672"
< "0060773","cleft lip-palate-ectodermal dysplasia syndrome","mondo","0009151"
< "0060772","dextro-looped transposition of the great arteries 3","icd10cm","Q20.3"
< "0060772","dextro-looped transposition of the great arteries 3","mondo","0013463"
< "0060771","dextro-looped transposition of the great arteries 1","icd10cm","Q20.3"
< "0060771","dextro-looped transposition of the great arteries 1","mondo","0012128"
< "0060770","dextro-looped transposition of the great arteries","icd10cm","Q20.3"
< "0060770","dextro-looped transposition of the great arteries","mondo","0019443"
< "0060777","congenital secretory sodium diarrhea 8","icd10cm","P78.3"
< "0060777","congenital secretory sodium diarrhea 8","mondo","0014808"
< "2871","endometrial carcinoma","mesh","D016889"
< "2871","endometrial carcinoma","mesh","D018269"
< "2871","endometrial carcinoma","umls","C0206687"
< "2871","endometrial carcinoma","umls","C0476089"
< "2871","endometrial carcinoma","mondo","0002447"
< "0060775","microvillus inclusion disease","icd10cm","P78.3"
< "0060775","microvillus inclusion disease","mesh","C537470"
< "0060775","microvillus inclusion disease","mondo","0009635"
< "0060378","orofaciodigital syndrome VIII","mesh","C557820"
< "0060378","orofaciodigital syndrome VIII","umls","C0796101"
< "0060378","orofaciodigital syndrome VIII","mondo","0010336"
< "13918","somatization disorder","icd10cm","F45.0"
< "13918","somatization disorder","icd9cm","300.81"
< "13918","somatization disorder","mesh","D013001"
< "13918","somatization disorder","umls","C0520482"
< "13918","somatization disorder","mondo","0001830"
< "8687","skin carcinoma in situ","icd10cm","D04"
< "8687","skin carcinoma in situ","icd10cm","D04.0"
< "8687","skin carcinoma in situ","icd10cm","D04.2"
< "8687","skin carcinoma in situ","icd10cm","D04.3"
< "8687","skin carcinoma in situ","icd10cm","D04.4"
< "8687","skin carcinoma in situ","icd10cm","D04.6"
< "8687","skin carcinoma in situ","icd10cm","D04.7"
< "8687","skin carcinoma in situ","icd10cm","D04.9"
< "8687","skin carcinoma in situ","icd9cm","232"
< "8687","skin carcinoma in situ","icd9cm","232.0"
< "8687","skin carcinoma in situ","icd9cm","232.2"
< "8687","skin carcinoma in situ","icd9cm","232.3"
< "8687","skin carcinoma in situ","icd9cm","232.4"
< "8687","skin carcinoma in situ","icd9cm","232.5"
< "8687","skin carcinoma in situ","icd9cm","232.6"
< "8687","skin carcinoma in situ","icd9cm","232.7"
< "8687","skin carcinoma in situ","icd9cm","232.9"
< "8687","skin carcinoma in situ","umls","C0154073"
< "8687","skin carcinoma in situ","umls","C0154074"
< "8687","skin carcinoma in situ","umls","C0154077"
< "8687","skin carcinoma in situ","umls","C0154078"
< "8687","skin carcinoma in situ","umls","C0154079"
< "8687","skin carcinoma in situ","umls","C0154080"
< "8687","skin carcinoma in situ","umls","C0154081"
< "8687","skin carcinoma in situ","umls","C0347139"
< "8687","skin carcinoma in situ","mondo","0004641"
< "5768","Nager acrofacial dysostosis","umls","C1332140"
< "5768","Nager acrofacial dysostosis","mondo","0007943"
---
> "2556","relapsing polychondritis","icd10cm","M94.1"
> "2556","relapsing polychondritis","mesh","D011081"
> "2556","relapsing polychondritis","umls","C0032453"
> "2556","relapsing polychondritis","mondo","0019125"
> "0050949","autosomal recessive hypophosphatemic rickets","mondo","0017324"
> "0050948","autosomal dominant hypophosphatemic rickets","mondo","0008660"
> "0050947","hereditary hypophosphatemic rickets with hypercalciuria","mondo","0009431"
> "0050946","Charlevoix-Saguenay spastic ataxia","mesh","C536787"
> "0050946","Charlevoix-Saguenay spastic ataxia","mondo","0010041"
> "0050945","spastic ataxia 7","mondo","0007165"
> "0050944","spastic ataxia 5","mondo","0013776"
> "0050943","spastic ataxia 4","mondo","0013354"
> "0050942","spastic ataxia 3","mondo","0012664"
> "0050941","spastic ataxia 2","mondo","0012651"
> "1412","bacteriuria","icd10cm","R82.71"
> "1412","bacteriuria","mesh","D001437"
> "1412","bacteriuria","umls","C0004659"
> "1412","bacteriuria","mondo","0001882"
> "1414","ovarian dysfunction","icd9cm","256.3"
> "1414","ovarian dysfunction","icd9cm","256.39"
> "1414","ovarian dysfunction","umls","C0029697"
> "1414","ovarian dysfunction","mondo","0001889"
> "1415","gyrate atrophy","mesh","D015799"
> "1415","gyrate atrophy","umls","C0018425"
> "1415","gyrate atrophy","mondo","0009796"
> "1417","choroid disease","icd10cm","H31.9"
> "1417","choroid disease","icd9cm","363.9"
> "1417","choroid disease","mesh","D015862"
> "1417","choroid disease","umls","C0008521"
> "1417","choroid disease","mondo","0001898"
> "0110205","Charcot-Marie-Tooth disease dominant intermediate E","icd10cm","G60.0"
> "0110205","Charcot-Marie-Tooth disease dominant intermediate E","mondo","0013758"
> "13919","irregular astigmatism","icd10cm","H52.21"
> "13919","irregular astigmatism","icd9cm","367.22"
> "13919","irregular astigmatism","umls","C0152194"
> "13919","irregular astigmatism","mondo","0001831"
> "4209","brainstem intraparenchymal clear cell meningioma","umls","C1332612"
> "4209","brainstem intraparenchymal clear cell meningioma","mondo","0002916"
8411,8412c17043,17050
< "2877","larynx sarcoma","umls","C1334377"
< "2877","larynx sarcoma","mondo","0002448"
---
> "4203","brain stem cancer","icd10cm","C71.7"
> "4203","brain stem cancer","icd9cm","191.7"
> "4203","brain stem cancer","mesh","D020295"
> "4203","brain stem cancer","umls","C0153641"
> "4203","brain stem cancer","umls","C0677866"
> "4203","brain stem cancer","umls","C0751886"
> "4203","brain stem cancer","umls","C1332192"
> "4203","brain stem cancer","mondo","0002912"
8417a17056,17058
> "4201","peroneal neuropathy","mesh","D020427"
> "4201","peroneal neuropathy","umls","C0747533"
> "4201","peroneal neuropathy","mondo","0002910"
8422,8428c17063,17068
< "2876","laryngeal squamous cell carcinoma","umls","C0280324"
< "2876","laryngeal squamous cell carcinoma","mondo","0005595"
< "8469","influenza","icd10cm","J11.1"
< "8469","influenza","icd9cm","487"
< "8469","influenza","mesh","D007251"
< "8469","influenza","umls","C0021400"
< "8469","influenza","mondo","0005812"
---
> "4205","cerebellum cancer","icd10cm","C71.6"
> "4205","cerebellum cancer","icd9cm","191.6"
> "4205","cerebellum cancer","mesh","D002528"
> "4205","cerebellum cancer","umls","C0007762"
> "4205","cerebellum cancer","umls","C0153640"
> "4205","cerebellum cancer","mondo","0002913"
8431,8432c17071,17074
< "3118","hepatobiliary disease","umls","C0267792"
< "3118","hepatobiliary disease","mondo","0002515"
---
> "5564","fallopian tube teratoma","umls","C1517127"
> "5564","fallopian tube teratoma","mondo","0003515"
> "5565","adult teratoma","umls","C1368898"
> "5565","adult teratoma","mondo","0003516"
8434a17077,17080
> "5567","ovarian germ cell teratoma","umls","C0280131"
> "5567","ovarian germ cell teratoma","mondo","0005602"
> "5560","mediastinal mesenchymal tumor","umls","C1334669"
> "5560","mediastinal mesenchymal tumor","mondo","0003512"
8441,8452c17087,17089
< "0060170","generalized epilepsy with febrile seizures plus","icd10cm","G40.3"
< "0060170","generalized epilepsy with febrile seizures plus","mondo","0018214"
< "1254","trichostrongylosis","icd10cm","B81.2"
< "1254","trichostrongylosis","icd9cm","127.6"
< "1254","trichostrongylosis","mesh","D014253"
< "1254","trichostrongylosis","umls","C0040948"
< "1254","trichostrongylosis","mondo","0005995"
< "0060175","succinic semialdehyde dehydrogenase deficiency","mesh","C535803"
< "0060175","succinic semialdehyde dehydrogenase deficiency","mondo","0010083"
< "0060174","GABA aminotransferase deficiency","mondo","0013166"
< "0060179","Renpenning syndrome","icd10cm","Q87.5"
< "0060179","Renpenning syndrome","mondo","0010653"
---
> "308","early myoclonic encephalopathy","mesh","D004831"
> "308","early myoclonic encephalopathy","umls","C0014550"
> "308","early myoclonic encephalopathy","mondo","0016022"
8461,8471c17098,17103
< "3953","adrenal gland cancer","icd10cm","C74"
< "3953","adrenal gland cancer","icd10cm","C74.9"
< "3953","adrenal gland cancer","icd9cm","194.0"
< "3953","adrenal gland cancer","mesh","D000310"
< "3953","adrenal gland cancer","umls","C0001624"
< "3953","adrenal gland cancer","umls","C0750887"
< "3953","adrenal gland cancer","mondo","0002817"
< "0110260","cataract 7","icd10cm","Q12.0"
< "0110260","cataract 7","mondo","0007279"
< "3950","adrenal carcinoma","umls","C1370740"
< "3950","adrenal carcinoma","mondo","0002814"
---
> "302","substance abuse","mesh","D019966"
> "302","substance abuse","umls","C0013146"
> "302","substance abuse","mondo","0002491"
> "303","substance-related disorder","mesh","D019966"
> "303","substance-related disorder","umls","C0236969"
> "303","substance-related disorder","mondo","0002494"
8481a17114,17119
> "11212","hydrophthalmos","icd10cm","Q15.0"
> "11212","hydrophthalmos","icd9cm","743.2"
> "11212","hydrophthalmos","icd9cm","743.20"
> "11212","hydrophthalmos","mesh","D006871"
> "11212","hydrophthalmos","umls","C0020302"
> "11212","hydrophthalmos","mondo","0006788"
8484,8498c17122,17129
< "4114","uterine body mixed cancer","umls","C1334628"
< "4114","uterine body mixed cancer","mondo","0002879"
< "4115","ovarian mesodermal adenosarcoma","umls","C1335169"
< "4115","ovarian mesodermal adenosarcoma","mondo","0002880"
< "4112","cervical carcinosarcoma","umls","C1332917"
< "4112","cervical carcinosarcoma","umls","C1516420"
< "4112","cervical carcinosarcoma","umls","C1518168"
< "4112","cervical carcinosarcoma","mondo","0002877"
< "4113","uterine corpus adenosarcoma","umls","C1336917"
< "4113","uterine corpus adenosarcoma","mondo","0002878"
< "4110","parasitic ectoparasitic infectious disease","mesh","D004478"
< "4110","parasitic ectoparasitic infectious disease","umls","C0013578"
< "4110","parasitic ectoparasitic infectious disease","mondo","0002875"
< "4111","cervical adenosarcoma","umls","C1516426"
< "4111","cervical adenosarcoma","mondo","0002876"
---
> "11211","buphthalmos","icd9cm","743.21"
> "11211","buphthalmos","umls","C0311251"
> "11211","buphthalmos","mondo","0009277"
> "11217","chronic tympanitis","icd10cm","H73.1"
> "11217","chronic tympanitis","icd10cm","H73.10"
> "11217","chronic tympanitis","icd9cm","384.1"
> "11217","chronic tympanitis","umls","C0395849"
> "11217","chronic tympanitis","mondo","0001227ub"
8503,8622c17134,17186
< "1381","Fox-Fordyce disease","icd10cm","L75.2"
< "1381","Fox-Fordyce disease","icd9cm","705.82"
< "1381","Fox-Fordyce disease","mesh","D005588"
< "1381","Fox-Fordyce disease","umls","C0016632"
< "1381","Fox-Fordyce disease","mondo","0006553"
< "75","lymphatic system disease","mesh","D008206"
< "75","lymphatic system disease","umls","C0024228"
< "75","lymphatic system disease","mondo","0005833"
< "0111061","familial hypobetalipoproteinemia 2","mondo","0011505"
< "5137","pericardium leiomyoma","umls","C1335380"
< "5137","pericardium leiomyoma","mondo","0003294"
< "7429","childhood brain germinoma","umls","C1332948"
< "7429","childhood brain germinoma","mondo","0004217"
< "4448","macular degeneration","umls","C0024437"
< "4448","macular degeneration","mondo","0003004"
< "0110841","Usher syndrome type 3A","icd10cm","H35.5"
< "0110841","Usher syndrome type 3A","mondo","0010170"
< "5158","pleural cancer","icd10cm","C38.4"
< "5158","pleural cancer","icd9cm","163"
< "5158","pleural cancer","icd9cm","163.9"
< "5158","pleural cancer","mesh","D010997"
< "5158","pleural cancer","umls","C0032229"
< "5158","pleural cancer","umls","C0153494"
< "5158","pleural cancer","mondo","0006294"
< "988","mitral valve prolapse","mesh","D008945"
< "988","mitral valve prolapse","umls","C0026267"
< "988","mitral valve prolapse","mondo","0004910"
< "5062","phencyclidine abuse","mesh","D010623"
< "5062","phencyclidine abuse","umls","C0031391"
< "5062","phencyclidine abuse","mondo","0005912"
< "12638","hypertrophic pyloric stenosis","icd10cm","Q40.0"
< "12638","hypertrophic pyloric stenosis","icd9cm","750.5"
< "12638","hypertrophic pyloric stenosis","mesh","D046248"
< "12638","hypertrophic pyloric stenosis","umls","C0700639"
< "12638","hypertrophic pyloric stenosis","mondo","0001560"
< "5015","fibrolamellar carcinoma","mesh","C537258"
< "5015","fibrolamellar carcinoma","umls","C0334287"
< "5015","fibrolamellar carcinoma","mondo","0006210"
< "4062","testis sarcoma","umls","C1336727"
< "4062","testis sarcoma","mondo","0002861"
< "4060","breast rhabdomyosarcoma","umls","C1332637"
< "4060","breast rhabdomyosarcoma","mondo","0002859"
< "4061","testis rhabdomyosarcoma","umls","C1336726"
< "4061","testis rhabdomyosarcoma","mondo","0002860"
< "4066","anus rhabdomyosarcoma","umls","C1332276"
< "4066","anus rhabdomyosarcoma","mondo","0002864"
< "10852","middle ear cholesterol granuloma","icd9cm","385.82"
< "10852","middle ear cholesterol granuloma","umls","C0155492"
< "10852","middle ear cholesterol granuloma","mondo","0001141"
< "4064","bile duct sarcoma","umls","C2205442"
< "4064","bile duct sarcoma","mondo","0002862"
< "13774","Addison's disease","icd10cm","E27.1"
< "13774","Addison's disease","mesh","D000224"
< "13774","Addison's disease","umls","C0001403"
< "13774","Addison's disease","mondo","0009410"
< "11506","suppurative otitis media","icd10cm","H66"
< "11506","suppurative otitis media","icd10cm","H66.4"
< "11506","suppurative otitis media","icd10cm","H66.40"
< "11506","suppurative otitis media","icd9cm","382"
< "11506","suppurative otitis media","icd9cm","382.4"
< "11506","suppurative otitis media","mesh","D010035"
< "11506","suppurative otitis media","umls","C0029888"
< "11506","suppurative otitis media","mondo","0005975"
< "11507","rumination disorder","icd9cm","307.53"
< "11507","rumination disorder","mesh","D019959"
< "11507","rumination disorder","umls","C0154575"
< "11507","rumination disorder","mondo","0001301"
< "13778","chancroid","icd10cm","A57"
< "13778","chancroid","icd9cm","099.0"
< "13778","chancroid","mesh","D002602"
< "13778","chancroid","umls","C0007947"
< "13778","chancroid","mondo","0001797"
< "0050848","obstructive sleep apnea","icd10cm","G47.33"
< "0050848","obstructive sleep apnea","icd9cm","327.23"
< "0050848","obstructive sleep apnea","mesh","D020181"
< "0050848","obstructive sleep apnea","umls","C0520679"
< "0050848","obstructive sleep apnea","mondo","0007147"
< "9507","ethmoid sinusitis","icd10cm","J32.2"
< "9507","ethmoid sinusitis","mesh","D015521"
< "9507","ethmoid sinusitis","umls","C0015029"
< "9507","ethmoid sinusitis","mondo","0005756"
< "3603","mucinous cystadenocarcinoma","mesh","D018282"
< "3603","mucinous cystadenocarcinoma","umls","C0206699"
< "3603","mucinous cystadenocarcinoma","mondo","0005858"
< "3602","toxic encephalopathy","mesh","D020258"
< "3602","toxic encephalopathy","umls","C0235032"
< "3602","toxic encephalopathy","mondo","0005527"
< "0080047","pseudoachondroplasia","mesh","C535819"
< "0080047","pseudoachondroplasia","mondo","0008322"
< "3605","ovarian cystadenocarcinoma","umls","C1096638"
< "3605","ovarian cystadenocarcinoma","mondo","0002702"
< "3604","ovarian mucinous cystadenocarcinoma","umls","C0279665"
< "3604","ovarian mucinous cystadenocarcinoma","mondo","0002701"
< "3608","appendix adenocarcinoma","umls","C0238003"
< "3608","appendix adenocarcinoma","mondo","0006087"
< "3413","alpha-mannosidosis","mesh","D008363"
< "3413","alpha-mannosidosis","umls","C0024748"
< "3413","alpha-mannosidosis","mondo","0009561"
< "0090053","episodic kinesigenic dyskinesia 1","icd10cm","G24.8"
< "0090053","episodic kinesigenic dyskinesia 1","mondo","0007494"
< "7551","gonorrhea","icd10cm","A54"
< "7551","gonorrhea","icd10cm","A54.9"
< "7551","gonorrhea","icd9cm","098"
< "7551","gonorrhea","mesh","D006069"
< "7551","gonorrhea","umls","C0018081"
< "7551","gonorrhea","mondo","0004277"
< "0110917","hereditary spherocytosis type 2","mondo","0000913"
< "0110916","hereditary spherocytosis type 1","mondo","0008447"
< "0110914","infantile hypophosphatasia","mondo","0009427"
< "0110913","adult hypophosphatasia","mondo","0007798"
< "0110912","leukocyte adhesion deficiency 3","mondo","0013016"
< "0110910","leukocyte adhesion deficiency 1","mondo","0007293"
< "0110355","retinitis pigmentosa 32","icd10cm","H35.5"
< "0110355","retinitis pigmentosa 32","mondo","0012363"
< "1382","miliaria","icd10cm","L74.3"
< "1382","miliaria","mesh","D008883"
< "1382","miliaria","umls","C0026113"
< "1382","miliaria","mondo","0006580"
< "0110919","hereditary spherocytosis type 4","mondo","0012981"
< "0110918","hereditary spherocytosis type 3","mondo","0010053"
---
> "12783","migraine without aura","icd10cm","G43.0"
> "12783","migraine without aura","icd10cm","G43.009"
> "12783","migraine without aura","icd9cm","346.1"
> "12783","migraine without aura","mesh","D020326"
> "12783","migraine without aura","umls","C0338480"
> "12783","migraine without aura","mondo","0011847"
> "10608","celiac disease","icd10cm","K90.0"
> "10608","celiac disease","icd9cm","579.0"
> "10608","celiac disease","mesh","D002446"
> "10608","celiac disease","umls","C0007570"
> "10608","celiac disease","mondo","0005130"
> "14271","acute cholangitis","umls","C0267917"
> "14271","acute cholangitis","mondo","0001930"
> "14270","ascending cholangitis","icd10cm","K83.0"
> "14270","ascending cholangitis","umls","C0311273"
> "14270","ascending cholangitis","mondo","0001929"
> "14276","shoulder impingement syndrome","icd10cm","M75.4"
> "14276","shoulder impingement syndrome","mesh","D019534"
> "14276","shoulder impingement syndrome","umls","C0376685"
> "14276","shoulder impingement syndrome","mondo","0006968"
> "5016","hepatocellular clear cell carcinoma","umls","C1333067"
> "5016","hepatocellular clear cell carcinoma","mondo","0003243"
> "10326","Caplan's syndrome","mesh","D002205"
> "10326","Caplan's syndrome","umls","C0006915"
> "10326","Caplan's syndrome","mondo","0005690"
> "4893","middle ear carcinoma","umls","C1334760"
> "4893","middle ear carcinoma","mondo","0003190"
> "10328","siderosis","icd10cm","J63.4"
> "10328","siderosis","mesh","D012806"
> "10328","siderosis","umls","C0037061"
> "10328","siderosis","mondo","0008346"
> "4890","juvenile myoclonic epilepsy","mesh","D020190"
> "4890","juvenile myoclonic epilepsy","umls","C0270853"
> "4890","juvenile myoclonic epilepsy","mondo","0009696"
> "4896","bile duct adenocarcinoma","umls","C1370800"
> "4896","bile duct adenocarcinoma","mondo","0003193"
> "4895","rete ovarii neoplasm","umls","C1514909"
> "4895","rete ovarii neoplasm","mondo","0003192"
> "6118","renal pelvis inverted papilloma","umls","C1335751"
> "6118","renal pelvis inverted papilloma","mondo","0003776"
> "6119","renal pelvis urothelial papilloma","umls","C1514844"
> "6119","renal pelvis urothelial papilloma","mondo","0003777"
> "6114","cerebral convexity meningioma","mesh","D008579"
> "6114","cerebral convexity meningioma","umls","C0751303"
> "6114","cerebral convexity meningioma","mondo","0003774"
> "6115","lateral ventricle meningioma","umls","C1334380"
> "6115","lateral ventricle meningioma","mondo","0003775"
> "6110","jugular foramen meningioma","umls","C1334298"
> "6110","jugular foramen meningioma","mondo","0003771"
> "6112","cerebral meningioma","umls","C0542564"
> "6112","cerebral meningioma","mondo","0003772"
> "6113","intracerebral cystic meningioma","umls","C1334236"
> "6113","intracerebral cystic meningioma","mondo","0003773"
8640,8660c17204,17214
< "11432","endometriosis of ovary","icd10cm","N80.1"
< "11432","endometriosis of ovary","icd9cm","617.1"
< "11432","endometriosis of ovary","umls","C0156344"
< "11432","endometriosis of ovary","mondo","0006337"
< "0060230","basal ganglia calcification","mesh","C536275"
< "0060230","basal ganglia calcification","umls","C0393590"
< "0060230","basal ganglia calcification","mondo","0008947"
< "2354","myelophthisic anemia","icd10cm","D61.82"
< "2354","myelophthisic anemia","mesh","D000750"
< "2354","myelophthisic anemia","umls","C0002890"
< "2354","myelophthisic anemia","mondo","0005868"
< "2355","anemia","icd10cm","D64.9"
< "2355","anemia","icd9cm","285.9"
< "2355","anemia","mesh","D000740"
< "2355","anemia","umls","C0002871"
< "2355","anemia","mondo","0002280"
< "3905","lung carcinoma","icd10cm","C34.90"
< "3905","lung carcinoma","umls","C0684249"
< "3905","lung carcinoma","mondo","0005138"
< "0050541","Charcot-Marie-Tooth disease type 4","mondo","0018995"
< "0050540","Charcot-Marie-Tooth disease type 3","mondo","0007790"
---
> "10927","gastrojejunal ulcer","icd10cm","K28.0"
> "10927","gastrojejunal ulcer","icd9cm","534.0"
> "10927","gastrojejunal ulcer","umls","C0156042"
> "10927","gastrojejunal ulcer","mondo","0001155"
> "7930","glandular-alveolar pattern testicular yolk sac tumor","umls","C1515305"
> "7930","glandular-alveolar pattern testicular yolk sac tumor","mondo","0004402"
> "7933","childhood precursor T-lymphoblastic lymphoma/leukemia","umls","C1332997"
> "7933","childhood precursor T-lymphoblastic lymphoma/leukemia","mondo","0004403"
> "7280","congenital epulis","mesh","D005887"
> "7280","congenital epulis","umls","C0376319"
> "7280","congenital epulis","mondo","0015528"
8666,8667c17220,17224
< "0050545","visceral heterotaxy","mondo","0018677"
< "0050012","chikungunya","mondo","0017941"
---
> "9108","uterus carcinoma in situ","icd9cm","233.2"
> "9108","uterus carcinoma in situ","umls","C0154086"
> "9108","uterus carcinoma in situ","mondo","0004710"
> "7936","refractory T lymphoblastic leukemia/lymphoma","umls","C0854859"
> "7936","refractory T lymphoblastic leukemia/lymphoma","mondo","0004404"
8683,8687c17240,17244
< "12287","Crimean-Congo hemorrhagic fever","icd10cm","A98.0"
< "12287","Crimean-Congo hemorrhagic fever","icd9cm","065.0"
< "12287","Crimean-Congo hemorrhagic fever","mesh","D006479"
< "12287","Crimean-Congo hemorrhagic fever","umls","C0019099"
< "12287","Crimean-Congo hemorrhagic fever","mondo","0020501"
---
> "0070140","autosomal recessive cutis laxa type IIC","icd10cm","Q82.8"
> "0070140","autosomal recessive cutis laxa type IIC","mondo","0027462"
> "0070143","autosomal recessive cutis laxa type III","mesh","C535990"
> "0070143","autosomal recessive cutis laxa type III","umls","C0268354"
> "0070143","autosomal recessive cutis laxa type III","mondo","0017569"
8696,8697c17253
< "4451","renal carcinoma","umls","C1378703"
< "4451","renal carcinoma","mondo","0005206"
---
> "0050787","juvenile polyposis syndrome","mondo","0008276"
8705,8722c17261,17269
< "3737","verrucous carcinoma","mesh","D018289"
< "3737","verrucous carcinoma","umls","C0206706"
< "3737","verrucous carcinoma","mondo","0006006"
< "4947","cholangiocarcinoma","icd10cm","C22.1"
< "4947","cholangiocarcinoma","mesh","D018281"
< "4947","cholangiocarcinoma","umls","C0206698"
< "4947","cholangiocarcinoma","umls","C0280725"
< "4947","cholangiocarcinoma","mondo","0019087"
< "3733","theileriasis","mesh","D013801"
< "3733","theileriasis","umls","C0039753"
< "3733","theileriasis","mondo","0005978"
< "476","breast hemangioma","umls","C0853715"
< "476","breast hemangioma","mondo","0003126"
< "4691","malignant mediastinal neurogenic neoplasm","umls","C1334672"
< "4691","malignant mediastinal neurogenic neoplasm","mondo","0003098"
< "4922","breast secretory carcinoma","mesh","C537535"
< "4922","breast secretory carcinoma","umls","C0334371"
< "4922","breast secretory carcinoma","mondo","0003208"
---
> "0050782","Zollinger-Ellison syndrome","icd10cm","E16.4"
> "0050782","Zollinger-Ellison syndrome","mesh","D015043"
> "0050782","Zollinger-Ellison syndrome","umls","C0043515"
> "0050782","Zollinger-Ellison syndrome","mondo","0019610"
> "0050789","tarsal-carpal coalition syndrome","mondo","0008521"
> "0050788","proximal symphalangism","kegg","H00484"
> "0050788","proximal symphalangism","mondo","0008511"
> "0080191","PTEN hamartoma tumor syndrome","mondo","0017623"
> "0080190","malignant epithelioid hemangioendothelioma","mondo","0015523"
8724,8731c17271,17276
< "0090122","aromatase excess syndrome","icd10cm","E30.1"
< "0090122","aromatase excess syndrome","mondo","0007690"
< "0090125","COL4A1-related familial vascular leukoencephalopathy","mondo","0011865"
< "2133","central nervous system sarcoma","umls","C1332892"
< "2133","central nervous system sarcoma","mondo","0002217"
< "0090127","camptodactyly-arthropathy-coxa vara-pericarditis syndrome","mesh","C537560"
< "0090127","camptodactyly-arthropathy-coxa vara-pericarditis syndrome","umls","C1859690"
< "0090127","camptodactyly-arthropathy-coxa vara-pericarditis syndrome","mondo","0008828"
---
> "12298","intrahepatic gall duct cancer","icd9cm","155.1"
> "12298","intrahepatic gall duct cancer","umls","C0546835"
> "12298","intrahepatic gall duct cancer","mondo","0001487"
> "0080195","Marinesco-Sjogren syndrome","mondo","0009567"
> "0080194","Carey-Fineman-Ziter syndrome","mondo","0009700"
> "0080197","congenital muscular dystrophy with cataracts and intellectual disability","mondo","0024607"
8733,8739c17278,17283
< "0110702","hypotrichosis 5","mondo","0013017"
< "13589","female infertility of uterine origin","icd10cm","N97.2"
< "13589","female infertility of uterine origin","icd9cm","628.3"
< "13589","female infertility of uterine origin","umls","C0156416"
< "13589","female infertility of uterine origin","mondo","0001753"
< "0110700","hypotrichosis 3","mondo","0013514"
< "0110701","hypotrichosis 4","mondo","0007806"
---
> "0080199","colorectal carcinoma","mondo","0024331"
> "9146","visceral leishmaniasis","icd10cm","B55.0"
> "9146","visceral leishmaniasis","icd9cm","085.0"
> "9146","visceral leishmaniasis","mesh","D007898"
> "9146","visceral leishmaniasis","umls","C0023290"
> "9146","visceral leishmaniasis","mondo","0005445"
8747,8752c17291,17295
< "0110871","congenital stationary night blindness 2A","mondo","0010241"
< "0110872","holoprosencephaly 2","mondo","0007999"
< "0110705","hypotrichosis 8","mondo","0010206"
< "11726","Emery-Dreifuss muscular dystrophy","mesh","D020389"
< "11726","Emery-Dreifuss muscular dystrophy","umls","C0410189"
< "11726","Emery-Dreifuss muscular dystrophy","mondo","0016830"
---
> "12294","atypical depressive disorder","icd10cm","F32.89"
> "12294","atypical depressive disorder","icd9cm","296.82"
> "12294","atypical depressive disorder","umls","C0154437"
> "12294","atypical depressive disorder","mondo","0001485"
> "0111095","Fanconi anemia complementation group A","mondo","0009215"
8754,8757c17297
< "11724","limb-girdle muscular dystrophy","icd10cm","G71.0"
< "11724","limb-girdle muscular dystrophy","mesh","D049288"
< "11724","limb-girdle muscular dystrophy","umls","C0686353"
< "11724","limb-girdle muscular dystrophy","mondo","0016971"
---
> "0111097","Fanconi anemia complementation group J","mondo","0012187"
8759,8763c17299
< "11722","myotonic dystrophy type 1","icd10cm","G71.11"
< "11722","myotonic dystrophy type 1","icd9cm","359.21"
< "11722","myotonic dystrophy type 1","mesh","D009223"
< "11722","myotonic dystrophy type 1","umls","C0027126"
< "11722","myotonic dystrophy type 1","mondo","0008056"
---
> "0111091","Fanconi anemia complementation group I","mondo","0012186"
8769,8806c17305,17308
< "11729","Lyme disease","icd10cm","A69.2"
< "11729","Lyme disease","icd10cm","A69.20"
< "11729","Lyme disease","icd9cm","088.81"
< "11729","Lyme disease","mesh","D008193"
< "11729","Lyme disease","mesh","D020852"
< "11729","Lyme disease","umls","C0024198"
< "11729","Lyme disease","umls","C0752235"
< "11729","Lyme disease","mondo","0019632"
< "2785","Dandy-Walker syndrome","icd10cm","Q03.1"
< "2785","Dandy-Walker syndrome","mesh","D003616"
< "2785","Dandy-Walker syndrome","umls","C0010964"
< "2785","Dandy-Walker syndrome","mondo","0009072"
< "10075","diphyllobothriasis","icd10cm","B70.0"
< "10075","diphyllobothriasis","icd9cm","123.4"
< "10075","diphyllobothriasis","mesh","D004169"
< "10075","diphyllobothriasis","umls","C0012561"
< "10075","diphyllobothriasis","mondo","0015260"
< "10074","hymenolepiasis","icd10cm","B71.0"
< "10074","hymenolepiasis","icd9cm","123.6"
< "10074","hymenolepiasis","mesh","D006925"
< "10074","hymenolepiasis","umls","C0020413"
< "10074","hymenolepiasis","mondo","0005802"
< "2784","lung sarcoma","umls","C0598790"
< "2784","lung sarcoma","mondo","0002426"
< "10079","cysticercosis","icd10cm","B69"
< "10079","cysticercosis","icd10cm","B69.9"
< "10079","cysticercosis","icd9cm","123.1"
< "10079","cysticercosis","mesh","D003551"
< "10079","cysticercosis","umls","C0010678"
< "10079","cysticercosis","mondo","0015484"
< "2641","ovarian germ cell monodermal and highly specialized teratoma","umls","C0280134"
< "2641","ovarian germ cell monodermal and highly specialized teratoma","mondo","0002372"
< "2645","benign mesothelioma","icd10cm","C45"
< "2645","benign mesothelioma","icd10cm","C45.9"
< "2645","benign mesothelioma","mesh","D008654"
< "2645","benign mesothelioma","umls","C0025500"
< "2645","benign mesothelioma","mondo","0002373"
< "0070095","oculocutaneous albinism type IB","mondo","0011749"
---
> "0050161","lower respiratory tract disease","icd9cm","478.1"
> "0050161","lower respiratory tract disease","icd9cm","478.19"
> "0050161","lower respiratory tract disease","umls","C0029581"
> "0050161","lower respiratory tract disease","mondo","0000270"
8807a17310,17314
> "0050166","tuberculous salpingitis","icd10cm","A18.17"
> "0050166","tuberculous salpingitis","icd9cm","016.6"
> "0050166","tuberculous salpingitis","umls","C0152828"
> "0050166","tuberculous salpingitis","mondo","0000271"
> "0050169","cutaneous lupus erythematosus","mondo","0005282"
8809,8849c17316,17333
< "9210","geniculate herpes zoster","icd10cm","B02.21"
< "9210","geniculate herpes zoster","icd9cm","053.11"
< "9210","geniculate herpes zoster","mesh","D016697"
< "9210","geniculate herpes zoster","umls","C0017409"
< "9210","geniculate herpes zoster","mondo","0005769"
< "6263","inflammatory breast carcinoma","mesh","D058922"
< "6263","inflammatory breast carcinoma","umls","C0278601"
< "6263","inflammatory breast carcinoma","mondo","0006804"
< "0110676","congenital myasthenic syndrome 13","mondo","0013883"
< "0110677","congenital myasthenic syndrome 4B","mondo","0014586"
< "12365","malaria","icd10cm","B54"
< "12365","malaria","icd9cm","084"
< "12365","malaria","icd9cm","084.6"
< "12365","malaria","mesh","D008288"
< "12365","malaria","umls","C0024530"
< "12365","malaria","mondo","0005136"
< "0110675","congenital myasthenic syndrome 11","mondo","0014588"
< "0050495","exanthema subitum","icd10cm","B08.2"
< "0050495","exanthema subitum","icd10cm","B08.20"
< "0050495","exanthema subitum","icd9cm","058.1"
< "0050495","exanthema subitum","icd9cm","058.10"
< "0050495","exanthema subitum","mesh","D005077"
< "0050495","exanthema subitum","umls","C0015231"
< "0050495","exanthema subitum","mondo","0000337"
< "0110673","congenital myasthenic syndrome 19","mondo","0014745"
< "12361","Graves' disease","icd10cm","E05.0"
< "12361","Graves' disease","mesh","D006111"
< "12361","Graves' disease","umls","C0018213"
< "12361","Graves' disease","mondo","0005364"
< "0110671","congenital myasthenic syndrome 6","mondo","0009689"
< "0070093","schizophrenia 18","mondo","0014092"
< "0070092","schizophrenia 16","mondo","0013506"
< "0070091","schizophrenia 15","mondo","0013498"
< "0070090","schizophrenia 14","mondo","0012879"
< "0070097","oculocutaneous albinism type III","mondo","0008747"
< "0070096","oculocutaneous albinism type II","mondo","0008746"
< "12369","prolapse of urethra","icd10cm","N81.0"
< "12369","prolapse of urethra","icd9cm","618.03"
< "12369","prolapse of urethra","umls","C0238502"
< "12369","prolapse of urethra","mondo","0001514"
< "0070094","oculocutaneous albinism type IA","mondo","0008745"
---
> "3429","inclusion body myositis","icd10cm","G72.41"
> "3429","inclusion body myositis","icd9cm","359.71"
> "3429","inclusion body myositis","mesh","D018979"
> "3429","inclusion body myositis","umls","C0238190"
> "3429","inclusion body myositis","mondo","0007827"
> "3428","granulomatous myositis","umls","C1334150"
> "3428","granulomatous myositis","mondo","0002644"
> "3421","trochlear nerve neoplasm","umls","C1263896"
> "3421","trochlear nerve neoplasm","mondo","0002642"
> "3426","vestibular disease","icd10cm","H81"
> "3426","vestibular disease","icd10cm","H81.9"
> "3426","vestibular disease","icd10cm","H81.90"
> "3426","vestibular disease","mesh","D015837"
> "3426","vestibular disease","umls","C0042594"
> "3426","vestibular disease","mondo","0002643"
> "0111271","Oliver-McFarlane syndrome","umls","C1848745"
> "0111270","isolated sulfite oxidase deficiency","umls","C0268624"
> "0111270","isolated sulfite oxidase deficiency","umls","C2931746"
8857,8866c17341,17364
< "5172","endometrium carcinoma in situ","icd10cm","D07.0"
< "5172","endometrium carcinoma in situ","umls","C0346191"
< "5172","endometrium carcinoma in situ","mondo","0003315"
< "6331","immature teratoma of ovary","umls","C0346182"
< "6331","immature teratoma of ovary","mondo","0018369"
< "5381","bile duct adenoma","mesh","D002759"
< "5381","bile duct adenoma","umls","C0008309"
< "5381","bile duct adenoma","mondo","0006108"
< "0110624","primary ciliary dyskinesia 30","icd10cm","Q34.8"
< "0110624","primary ciliary dyskinesia 30","mondo","0014465"
---
> "2001","neuroma","mesh","D009463"
> "2001","neuroma","umls","C0027858"
> "2001","neuroma","mondo","0002173"
> "2006","preretinal fibrosis","icd9cm","362.56"
> "2006","preretinal fibrosis","mesh","D019773"
> "2006","preretinal fibrosis","umls","C0339543"
> "2006","preretinal fibrosis","mondo","0002174"
> "4588","secretory meningioma","mesh","D008579"
> "4588","secretory meningioma","umls","C1384406"
> "4588","secretory meningioma","mondo","0003055"
> "0111277","mitochondrial trifunctional protein deficiency","umls","C1969443"
> "4858","pineal gland astrocytoma","umls","C0280795"
> "4858","pineal gland astrocytoma","mondo","0003171"
> "4856","gliofibroma","umls","C1266178"
> "4856","gliofibroma","mondo","0003170"
> "4855","diencephalic astrocytomas","umls","C1333284"
> "4855","diencephalic astrocytomas","mondo","0003169"
> "4586","familial meningioma","mesh","C537443"
> "4586","familial meningioma","umls","C1333989"
> "4586","familial meningioma","mondo","0011789"
> "4853","pilocytic astrocytoma of cerebellum","umls","C0349620"
> "4853","pilocytic astrocytoma of cerebellum","mondo","0003168"
> "4852","pleomorphic xanthoastrocytoma","umls","C0334586"
> "4852","pleomorphic xanthoastrocytoma","mondo","0016690"
8870,8878c17368,17381
< "5263","ovary leiomyosarcoma","umls","C1335163"
< "5263","ovary leiomyosarcoma","mondo","0003355"
< "9074","systemic lupus erythematosus","kegg","05322"
< "9074","systemic lupus erythematosus","icd10cm","M32"
< "9074","systemic lupus erythematosus","icd10cm","M32.9"
< "9074","systemic lupus erythematosus","icd9cm","710.0"
< "9074","systemic lupus erythematosus","mesh","D008180"
< "9074","systemic lupus erythematosus","umls","C0024141"
< "9074","systemic lupus erythematosus","mondo","0007915"
---
> "14174","central neurocytoma","mesh","D018306"
> "14174","central neurocytoma","umls","C0206719"
> "14174","central neurocytoma","mondo","0019134"
> "14175","von Hippel-Lindau disease","icd10cm","Q85.8"
> "14175","von Hippel-Lindau disease","mesh","D006623"
> "14175","von Hippel-Lindau disease","umls","C0019562"
> "14175","von Hippel-Lindau disease","mondo","0008667"
> "14176","selective IgG deficiency disease","icd10cm","D80.3"
> "14176","selective IgG deficiency disease","mesh","D017099"
> "14176","selective IgG deficiency disease","umls","C0162539"
> "14176","selective IgG deficiency disease","mondo","0001901"
> "14177","congenital hypogammaglobulinemia","icd9cm","279.04"
> "14177","congenital hypogammaglobulinemia","umls","C1457897"
> "14177","congenital hypogammaglobulinemia","mondo","0001902"
8901,8911c17404,17405
< "10457","Legionnaires' disease","icd10cm","A48.1"
< "10457","Legionnaires' disease","icd9cm","482.84"
< "10457","Legionnaires' disease","mesh","D007877"
< "10457","Legionnaires' disease","umls","C0023241"
< "10457","Legionnaires' disease","mondo","0005824"
< "10456","tonsillitis","icd10cm","J35.01"
< "10456","tonsillitis","icd9cm","474.00"
< "10456","tonsillitis","mesh","D014069"
< "10456","tonsillitis","umls","C0040425"
< "10456","tonsillitis","umls","C0149517"
< "10456","tonsillitis","mondo","0001039"
---
> "0040015","sulfonamide allergy","icd10cm","Z88.9"
> "0040015","sulfonamide allergy","umls","C0038757"
8913,8926c17407,17413
< "11983","Prader-Willi syndrome","icd10cm","Q87.1"
< "11983","Prader-Willi syndrome","icd9cm","759.81"
< "11983","Prader-Willi syndrome","mesh","D011218"
< "11983","Prader-Willi syndrome","umls","C0032897"
< "11983","Prader-Willi syndrome","mondo","0008300"
< "10459","common cold","icd10cm","J00"
< "10459","common cold","icd9cm","460"
< "10459","common cold","mesh","D003139"
< "10459","common cold","umls","C0009443"
< "10459","common cold","mondo","0005709"
< "10458","legionellosis","mesh","D007876"
< "10458","legionellosis","umls","C0023240"
< "10458","legionellosis","mondo","0005823"
< "0070328","adult hepatocellular carcinoma","umls","C0279607"
---
> "0040019","D-mannitol allergy","umls","C0571922"
> "11981","morbid obesity","icd9cm","278.01"
> "11981","morbid obesity","mesh","D009767"
> "11981","morbid obesity","umls","C0028756"
> "11981","morbid obesity","mondo","0005139"
> "0110203","Charcot-Marie-Tooth disease recessive intermediate D","icd10cm","G60.0"
> "0110203","Charcot-Marie-Tooth disease recessive intermediate D","mondo","0014467"
8936,8958d17422
< "0110452","dilated cardiomyopathy 1T","icd10cm","I42.0"
< "0110452","dilated cardiomyopathy 1T","mondo","0000911"
< "0110453","dilated cardiomyopathy 1EE","icd10cm","I42.0"
< "0110453","dilated cardiomyopathy 1EE","mondo","0013198"
< "0110450","dilated cardiomyopathy 1II","icd10cm","I42.0"
< "0110450","dilated cardiomyopathy 1II","mondo","0014073"
< "0110451","dilated cardiomyopathy 1O","icd10cm","I42.0"
< "0110451","dilated cardiomyopathy 1O","mondo","0012062"
< "0110456","dilated cardiomyopathy 1R","icd10cm","I42.0"
< "0110456","dilated cardiomyopathy 1R","mondo","0013261"
< "0110457","dilated cardiomyopathy 1Y","icd10cm","I42.0"
< "0110457","dilated cardiomyopathy 1Y","mondo","0012744"
< "0110454","dilated cardiomyopathy 1S","icd10cm","I42.0"
< "0110454","dilated cardiomyopathy 1S","mondo","0013262"
< "0110455","dilated cardiomyopathy 1U","icd10cm","I42.0"
< "0110455","dilated cardiomyopathy 1U","mondo","0013371"
< "0110458","dilated cardiomyopathy 1BB","icd10cm","I42.0"
< "0110458","dilated cardiomyopathy 1BB","mondo","0013030"
< "0110459","dilated cardiomyopathy 1FF","icd10cm","I42.0"
< "0110459","dilated cardiomyopathy 1FF","mondo","0013211"
< "3559","pseudomyxoma peritonei","mesh","D011553"
< "3559","pseudomyxoma peritonei","umls","C0033822"
< "3559","pseudomyxoma peritonei","mondo","0017048"
8964,8968c17428,17436
< "12096","sodoku disease","icd10cm","A25.0"
< "12096","sodoku disease","icd9cm","026.0"
< "12096","sodoku disease","mesh","D011906"
< "12096","sodoku disease","umls","C0152062"
< "12096","sodoku disease","mondo","0020532"
---
> "13168","prepuce cancer","icd10cm","C60.0"
> "13168","prepuce cancer","icd9cm","187.1"
> "13168","prepuce cancer","umls","C0153598"
> "13168","prepuce cancer","mondo","0001653"
> "10582","Refsum disease","icd10cm","G60.1"
> "10582","Refsum disease","icd9cm","356.3"
> "10582","Refsum disease","mesh","D012035"
> "10582","Refsum disease","umls","C0034960"
> "10582","Refsum disease","mondo","0009958"
8974a17443,17446
> "10587","Krabbe disease","icd10cm","E75.23"
> "10587","Krabbe disease","mesh","D007965"
> "10587","Krabbe disease","umls","C0023521"
> "10587","Krabbe disease","mondo","0009499"
8983a17456,17457
> "0110202","Charcot-Marie-Tooth disease dominant intermediate A","icd10cm","G60.0"
> "0110202","Charcot-Marie-Tooth disease dominant intermediate A","mondo","0011675"
8989,9008c17463,17480
< "9460","uterine corpus cancer","icd10cm","C54"
< "9460","uterine corpus cancer","icd10cm","C54.9"
< "9460","uterine corpus cancer","icd9cm","182"
< "9460","uterine corpus cancer","umls","C0153574"
< "9460","uterine corpus cancer","mondo","0006003"
< "1909","melanoma","kegg","05218"
< "1909","melanoma","mesh","D008545"
< "1909","melanoma","umls","C0025202"
< "1909","melanoma","mondo","0005105"
< "1799","islet cell tumor","icd10cm","C25.4"
< "1799","islet cell tumor","icd10cm","D13.7"
< "1799","islet cell tumor","mesh","D007516"
< "1799","islet cell tumor","umls","C0242363"
< "1799","islet cell tumor","umls","C0496784"
< "1799","islet cell tumor","mondo","0005815"
< "1798","pancreatic endocrine carcinoma","icd10cm","C25.4"
< "1798","pancreatic endocrine carcinoma","icd9cm","157.4"
< "1798","pancreatic endocrine carcinoma","mesh","D018273"
< "1798","pancreatic endocrine carcinoma","umls","C1328479"
< "1798","pancreatic endocrine carcinoma","mondo","0005893"
---
> "14350","suppurative thyroiditis","icd10cm","E06.0"
> "14350","suppurative thyroiditis","mesh","D013969"
> "14350","suppurative thyroiditis","umls","C0040150"
> "14350","suppurative thyroiditis","mondo","0001947"
> "14351","Riedel's fibrosing thyroiditis","icd10cm","E06.5"
> "14351","Riedel's fibrosing thyroiditis","umls","C0154162"
> "14351","Riedel's fibrosing thyroiditis","mondo","0001948"
> "11180","non-suppurative otitis media","icd10cm","H65"
> "11180","non-suppurative otitis media","icd10cm","H65.9"
> "11180","non-suppurative otitis media","icd10cm","H65.90"
> "11180","non-suppurative otitis media","icd9cm","381.4"
> "11180","non-suppurative otitis media","umls","C0271446"
> "11180","non-suppurative otitis media","mondo","0001212"
> "11181","serous glue ear","icd10cm","H65.2"
> "11181","serous glue ear","icd10cm","H65.20"
> "11181","serous glue ear","icd9cm","381.1"
> "11181","serous glue ear","umls","C0155421"
> "11181","serous glue ear","mondo","0001213"
9013,9127c17485,17521
< "4969","Gerstmann syndrome","mesh","D005862"
< "4969","Gerstmann syndrome","umls","C0017494"
< "4969","Gerstmann syndrome","mondo","0005773"
< "718","autoimmune hemolytic anemia","icd9cm","283.0"
< "718","autoimmune hemolytic anemia","mesh","D000744"
< "718","autoimmune hemolytic anemia","umls","C0002880"
< "718","autoimmune hemolytic anemia","mondo","0020108"
< "1793","pancreatic cancer","kegg","05212"
< "1793","pancreatic cancer","icd10cm","C25.0"
< "1793","pancreatic cancer","icd10cm","C25.1"
< "1793","pancreatic cancer","icd10cm","C25.2"
< "1793","pancreatic cancer","icd9cm","157.0"
< "1793","pancreatic cancer","icd9cm","157.1"
< "1793","pancreatic cancer","icd9cm","157.2"
< "1793","pancreatic cancer","icd9cm","157.8"
< "1793","pancreatic cancer","mesh","D010190"
< "1793","pancreatic cancer","umls","C0030297"
< "1793","pancreatic cancer","umls","C0153458"
< "1793","pancreatic cancer","umls","C0153459"
< "1793","pancreatic cancer","umls","C0153460"
< "1793","pancreatic cancer","umls","C0153463"
< "1793","pancreatic cancer","mondo","0009831"
< "0070229","intrahepatic cholestasis of pregnancy 3","mondo","0013995"
< "1791","peritoneal carcinoma","umls","C1514428"
< "1791","peritoneal carcinoma","mondo","0002113"
< "1790","malignant mesothelioma","mesh","C562839"
< "1790","malignant mesothelioma","umls","C0278752"
< "1790","malignant mesothelioma","umls","C0345967"
< "1790","malignant mesothelioma","umls","C0392400"
< "1790","malignant mesothelioma","umls","C1332338"
< "1790","malignant mesothelioma","mondo","0006292"
< "1796","pancreas sarcoma","umls","C1096346"
< "1796","pancreas sarcoma","mondo","0002117"
< "711","refractory hairy cell leukemia","umls","C0279780"
< "711","refractory hairy cell leukemia","mondo","0004110"
< "0050820","atrioventricular block","icd10cm","I44.3"
< "0050820","atrioventricular block","icd10cm","I44.30"
< "0050820","atrioventricular block","icd9cm","426.10"
< "0050820","atrioventricular block","mesh","D054537"
< "0050820","atrioventricular block","umls","C0004245"
< "0050820","atrioventricular block","mondo","0000465"
< "6759","bone lymphoma","umls","C1332582"
< "6759","bone lymphoma","mondo","0017814"
< "0050826","tricuspid valve disease","icd10cm","I07"
< "0050826","tricuspid valve disease","icd10cm","I07.9"
< "0050826","tricuspid valve disease","icd9cm","397.0"
< "0050826","tricuspid valve disease","umls","C0264776"
< "0050826","tricuspid valve disease","mondo","0000471"
< "13768","opisthorchiasis","icd10cm","B66.0"
< "13768","opisthorchiasis","icd9cm","121.0"
< "13768","opisthorchiasis","mesh","D009889"
< "13768","opisthorchiasis","umls","C0029106"
< "13768","opisthorchiasis","mondo","0005884"
< "6841","flat ductal epithelial atypia","umls","C1333620"
< "6841","flat ductal epithelial atypia","mondo","0004008"
< "10845","St. Louis encephalitis","icd10cm","A83.3"
< "10845","St. Louis encephalitis","icd9cm","062.3"
< "10845","St. Louis encephalitis","mesh","D004674"
< "10845","St. Louis encephalitis","umls","C0014060"
< "10845","St. Louis encephalitis","mondo","0005969"
< "1068","juvenile glaucoma","mondo","0020367"
< "10609","rickets","icd10cm","E55.0"
< "10609","rickets","icd9cm","268.0"
< "10609","rickets","mesh","D012279"
< "10609","rickets","umls","C0035579"
< "10609","rickets","umls","C0221468"
< "10609","rickets","mondo","0005520"
< "5301","fallopian tube clear cell adenocarcinoma","umls","C1333591"
< "5301","fallopian tube clear cell adenocarcinoma","mondo","0003383"
< "1062","Fanconi syndrome","mesh","D005198"
< "1062","Fanconi syndrome","umls","C0015624"
< "1062","Fanconi syndrome","umls","C0341703"
< "1062","Fanconi syndrome","mondo","0001083"
< "1064","cystinosis","mesh","D003554"
< "1064","cystinosis","umls","C2931187"
< "1064","cystinosis","mondo","0016239"
< "1067","open-angle glaucoma","icd10cm","H40.1"
< "1067","open-angle glaucoma","icd10cm","H40.10"
< "1067","open-angle glaucoma","icd10cm","H40.13"
< "1067","open-angle glaucoma","icd9cm","365.1"
< "1067","open-angle glaucoma","icd9cm","365.10"
< "1067","open-angle glaucoma","icd9cm","365.13"
< "1067","open-angle glaucoma","mesh","D005902"
< "1067","open-angle glaucoma","umls","C0017612"
< "1067","open-angle glaucoma","mondo","0005338"
< "5307","urethra clear cell adenocarcinoma","umls","C1336886"
< "5307","urethra clear cell adenocarcinoma","mondo","0003387"
< "12384","dysentery","icd9cm","009.2"
< "12384","dysentery","mesh","D004403"
< "12384","dysentery","umls","C0013369"
< "12384","dysentery","mondo","0001517"
< "0110298","autosomal recessive limb-girdle muscular dystrophy type 2N","icd10cm","G71.0"
< "0110298","autosomal recessive limb-girdle muscular dystrophy type 2N","mondo","0013162"
< "0110299","autosomal recessive limb-girdle muscular dystrophy type 2I","icd10cm","G71.0"
< "0110299","autosomal recessive limb-girdle muscular dystrophy type 2I","mondo","0011787"
< "0110294","autosomal recessive limb-girdle muscular dystrophy type 2T","icd10cm","G71.0"
< "0110294","autosomal recessive limb-girdle muscular dystrophy type 2T","mondo","0014142"
< "0110295","autosomal recessive limb-girdle muscular dystrophy type 2U","icd10cm","G71.0"
< "0110295","autosomal recessive limb-girdle muscular dystrophy type 2U","mondo","0014474"
< "0110296","autosomal recessive limb-girdle muscular dystrophy type 2M","icd10cm","G71.0"
< "0110296","autosomal recessive limb-girdle muscular dystrophy type 2M","mondo","0012699"
< "0110297","autosomal recessive limb-girdle muscular dystrophy type 2K","icd10cm","G71.0"
< "0110297","autosomal recessive limb-girdle muscular dystrophy type 2K","mondo","0012248"
< "0110290","autosomal recessive limb-girdle muscular dystrophy type 2X","mondo","0014782"
< "0110291","Leber congenital amaurosis 10","icd10cm","H35.5"
< "0110291","Leber congenital amaurosis 10","mondo","0012723"
< "0110292","autosomal recessive limb-girdle muscular dystrophy type 2O","icd10cm","G71.0"
< "0110292","autosomal recessive limb-girdle muscular dystrophy type 2O","mondo","0013161"
< "0110293","autosomal recessive limb-girdle muscular dystrophy type 2P","icd10cm","G71.0"
< "0110293","autosomal recessive limb-girdle muscular dystrophy type 2P","mondo","0013440"
< "593","agoraphobia","icd10cm","F40.0"
< "593","agoraphobia","icd10cm","F40.00"
< "593","agoraphobia","mesh","D000379"
< "593","agoraphobia","umls","C0001818"
< "593","agoraphobia","mondo","0003709"
---
> "11184","acute conjunctivitis","icd10cm","H10.02"
> "11184","acute conjunctivitis","icd9cm","372.03"
> "11184","acute conjunctivitis","umls","C0029668"
> "11184","acute conjunctivitis","mondo","0001214"
> "11189","pulp degeneration","icd10cm","K04.2"
> "11189","pulp degeneration","icd9cm","522.2"
> "11189","pulp degeneration","umls","C0034100"
> "11189","pulp degeneration","mondo","0001216"
> "10039","late congenital syphilis","icd10cm","A50.4"
> "10039","late congenital syphilis","icd10cm","A50.40"
> "10039","late congenital syphilis","icd10cm","A50.5"
> "10039","late congenital syphilis","icd10cm","A50.59"
> "10039","late congenital syphilis","icd9cm","090.4"
> "10039","late congenital syphilis","icd9cm","090.40"
> "10039","late congenital syphilis","icd9cm","090.5"
> "10039","late congenital syphilis","mesh","D009494"
> "10039","late congenital syphilis","umls","C0153132"
> "10039","late congenital syphilis","umls","C0153136"
> "10039","late congenital syphilis","mondo","0005821"
> "8622","measles","icd10cm","B05"
> "8622","measles","icd10cm","B05.9"
> "8622","measles","icd9cm","055"
> "8622","measles","mesh","D008457"
> "8622","measles","umls","C0025007"
> "8622","measles","mondo","0004619"
> "9547","non-secretory myeloma","umls","C0456845"
> "9547","non-secretory myeloma","mondo","0004817"
> "9544","refractory plasma cell neoplasm","umls","C0278620"
> "9544","refractory plasma cell neoplasm","mondo","0004816"
> "9540","vascular skin disease","icd9cm","709.1"
> "9540","vascular skin disease","mesh","D017445"
> "9540","vascular skin disease","umls","C0162819"
> "9540","vascular skin disease","mondo","0019293"
> "1085","Edwards syndrome","icd9cm","758.2"
> "1085","Edwards syndrome","mesh","D000073842"
> "1085","Edwards syndrome","umls","C0152096"
> "1085","Edwards syndrome","mondo","0018071"
9131a17526,17529
> "1081","mansonelliasis","icd10cm","B74.4"
> "1081","mansonelliasis","mesh","D008368"
> "1081","mansonelliasis","umls","C0024759"
> "1081","mansonelliasis","mondo","0005838"
9138,9186c17536,17553
< "599","specific phobia","icd10cm","F40.2"
< "599","specific phobia","mesh","C562465"
< "599","specific phobia","umls","C0236801"
< "599","specific phobia","mondo","0012000"
< "13080","Jaccoud's syndrome","icd10cm","M12.0"
< "13080","Jaccoud's syndrome","icd10cm","M12.00"
< "13080","Jaccoud's syndrome","icd9cm","714.4"
< "13080","Jaccoud's syndrome","umls","C0152084"
< "13080","Jaccoud's syndrome","mondo","0001629"
< "4325","Ebola hemorrhagic fever","icd10cm","A98.4"
< "4325","Ebola hemorrhagic fever","mesh","D019142"
< "4325","Ebola hemorrhagic fever","umls","C0282687"
< "4325","Ebola hemorrhagic fever","mondo","0005737"
< "4327","Marburg hemorrhagic fever","icd10cm","A98.3"
< "4327","Marburg hemorrhagic fever","mesh","D008379"
< "4327","Marburg hemorrhagic fever","umls","C0024788"
< "4327","Marburg hemorrhagic fever","mondo","0020500"
< "3140","scleredema adultorum","mesh","D012592"
< "3140","scleredema adultorum","umls","C0036413"
< "3140","scleredema adultorum","mondo","0006606"
< "3144","cutis laxa","icd10cm","Q82.8"
< "3144","cutis laxa","mesh","D003483"
< "3144","cutis laxa","umls","C0010495"
< "3144","cutis laxa","mondo","0016175"
< "3145","hyperlipoproteinemia type III","mesh","D006952"
< "3145","hyperlipoproteinemia type III","umls","C0020479"
< "3145","hyperlipoproteinemia type III","mondo","0018473"
< "3146","lipid metabolism disorder","mesh","D008052"
< "3146","lipid metabolism disorder","umls","C0023772"
< "3146","lipid metabolism disorder","mondo","0002525"
< "14040","autoimmune polyendocrine syndrome","icd10cm","E31.0"
< "14040","autoimmune polyendocrine syndrome","mesh","D016884"
< "14040","autoimmune polyendocrine syndrome","umls","C0085409"
< "14040","autoimmune polyendocrine syndrome","mondo","0017278"
< "14755","argininosuccinic aciduria","mesh","D056807"
< "14755","argininosuccinic aciduria","umls","C0268547"
< "14755","argininosuccinic aciduria","mondo","0008815"
< "5419","schizophrenia","icd10cm","F20"
< "5419","schizophrenia","icd10cm","F20.9"
< "5419","schizophrenia","icd9cm","295"
< "5419","schizophrenia","icd9cm","295.9"
< "5419","schizophrenia","icd9cm","295.90"
< "5419","schizophrenia","mesh","D012559"
< "5419","schizophrenia","umls","C0036341"
< "5419","schizophrenia","mondo","0005090"
< "14753","isovaleric acidemia","icd10cm","E71.110"
< "14753","isovaleric acidemia","mesh","C538167"
< "14753","isovaleric acidemia","umls","C0268575"
< "14753","isovaleric acidemia","mondo","0009475"
---
> "1089","tethered spinal cord syndrome","icd10cm","Q05"
> "1089","tethered spinal cord syndrome","icd10cm","Q05.9"
> "1089","tethered spinal cord syndrome","icd9cm","741"
> "1089","tethered spinal cord syndrome","mesh","D016135"
> "1089","tethered spinal cord syndrome","umls","C0080178"
> "1089","tethered spinal cord syndrome","mondo","0006995"
> "1088","meningocele","mesh","D008588"
> "1088","meningocele","umls","C0025299"
> "1088","meningocele","mondo","0001147"
> "12987","agranulocytosis","icd10cm","D70"
> "12987","agranulocytosis","mesh","D000380"
> "12987","agranulocytosis","umls","C0001824"
> "12987","agranulocytosis","mondo","0001609"
> "12986","leukostasis","mesh","D018921"
> "12986","leukostasis","umls","C0282548"
> "12986","leukostasis","mondo","0006831"
> "12984","vagus nerve neoplasm","umls","C1263901"
> "12984","vagus nerve neoplasm","mondo","0001608"
9195a17563,17568
> "0060381","orofaciodigital syndrome XI","mesh","C557821"
> "0060381","orofaciodigital syndrome XI","umls","C2752048"
> "0060381","orofaciodigital syndrome XI","mondo","0013035"
> "0060386","Chilblain lupus","mesh","C535924"
> "0060386","Chilblain lupus","umls","C0024145"
> "0060386","Chilblain lupus","mondo","0019557"
9199,9214c17572,17579
< "9281","phenylketonuria","icd9cm","270.1"
< "9281","phenylketonuria","mesh","D010661"
< "9281","phenylketonuria","mesh","D017042"
< "9281","phenylketonuria","umls","C0031485"
< "9281","phenylketonuria","umls","C0085547"
< "9281","phenylketonuria","mondo","0009861"
< "0080390","nephrotic syndrome type 1","mesh","C535761"
< "0080390","nephrotic syndrome type 1","umls","C0403399"
< "3963","thyroid carcinoma","mesh","D013964"
< "3963","thyroid carcinoma","umls","C0549473"
< "3963","thyroid carcinoma","mondo","0015075"
< "0060768","Smith-Magenis syndrome","icd10cm","Q93.5"
< "0060768","Smith-Magenis syndrome","mesh","D058496"
< "0060768","Smith-Magenis syndrome","mondo","0008434"
< "0060769","T-cell immunodeficiency, congenital alopecia, and nail dystrophy","icd10cm","D82.8"
< "0060769","T-cell immunodeficiency, congenital alopecia, and nail dystrophy","mondo","0011132"
---
> "0060384","acrofacial dysostosis, Catania type","mesh","C538182"
> "0060384","acrofacial dysostosis, Catania type","umls","C2931762"
> "0060384","acrofacial dysostosis, Catania type","mondo","0007045"
> "0060385","acrofacial dysostosis, Patagonia type","mesh","C538185"
> "0060385","acrofacial dysostosis, Patagonia type","umls","C1866168"
> "0060385","acrofacial dysostosis, Patagonia type","mondo","0011154"
> "0060389","chromosome 10q23 deletion syndrome","mesh","C567385"
> "0060389","chromosome 10q23 deletion syndrome","mondo","0012830"
9223,9237c17588,17596
< "13902","white piedra","icd10cm","B36.2"
< "13902","white piedra","icd9cm","111.2"
< "13902","white piedra","mesh","D010854"
< "13902","white piedra","umls","C0031898"
< "13902","white piedra","umls","C0040249"
< "13902","white piedra","mondo","0001827"
< "0060760","immunodeficiency with hyper-IgM type 4","icd10cm","D80.5"
< "0060760","immunodeficiency with hyper-IgM type 4","mondo","0011985"
< "0060761","familial chronic myelocytic leukemia-like syndrome","mondo","0010809"
< "0060762","lethal restrictive dermopathy","mesh","C536920"
< "0060762","lethal restrictive dermopathy","umls","C0406585"
< "0060762","lethal restrictive dermopathy","mondo","0010143"
< "0060763","X-linked juvenile retinoschisis 1","icd10cm","Q14.1"
< "0060763","X-linked juvenile retinoschisis 1","mondo","0010725"
< "0060764","autosomal recessive Robinow syndrome","mondo","0009999"
---
> "440","neuromuscular disease","icd10cm","G70.9"
> "440","neuromuscular disease","icd9cm","358"
> "440","neuromuscular disease","icd9cm","358.9"
> "440","neuromuscular disease","mesh","D009468"
> "440","neuromuscular disease","umls","C0027868"
> "440","neuromuscular disease","mondo","0019056"
> "447","renal tubular transport disease","mesh","D015499"
> "447","renal tubular transport disease","umls","C0035091"
> "447","renal tubular transport disease","mondo","0006510"
9250,9253c17609,17626
< "0060766","autosomal dominant Robinow syndrome 1","mondo","0024455"
< "0060767","autosomal dominant Robinow syndrome 3","mondo","0014819"
< "1520","colon carcinoma","umls","C0699790"
< "1520","colon carcinoma","mondo","0002032"
---
> "445","Bartter disease","icd10cm","E26.81"
> "445","Bartter disease","icd9cm","255.13"
> "445","Bartter disease","mesh","D001477"
> "445","Bartter disease","umls","C0004775"
> "445","Bartter disease","mondo","0015231"
> "6932","urinary bladder inverted papilloma","umls","C1511190"
> "6932","urinary bladder inverted papilloma","mondo","0004040"
> "6933","bladder transitional cell papilloma","umls","C0235754"
> "6933","bladder transitional cell papilloma","umls","C1384678"
> "6933","bladder transitional cell papilloma","mondo","0004041"
> "6931","papillary extrahepatic bile duct adenocarcinoma","umls","C0861858"
> "6931","papillary extrahepatic bile duct adenocarcinoma","mondo","0004039"
> "6936","ureter urothelial papilloma","umls","C1519823"
> "6936","ureter urothelial papilloma","mondo","0004044"
> "6934","urethra inverted papilloma","umls","C1336887"
> "6934","urethra inverted papilloma","mondo","0004042"
> "6935","ureter inverted papilloma","umls","C1336874"
> "6935","ureter inverted papilloma","mondo","0004043"
9261,9262c17634,17644
< "6939","childhood brain meningioma","umls","C1332949"
< "6939","childhood brain meningioma","mondo","0004046"
---
> "8696","subacute monocytic leukemia","icd9cm","206.2"
> "8696","subacute monocytic leukemia","umls","C0152275"
> "8696","subacute monocytic leukemia","mondo","0004644"
> "8691","mycosis fungoides","icd10cm","C84.0"
> "8691","mycosis fungoides","icd10cm","C84.00"
> "8691","mycosis fungoides","icd9cm","202.1"
> "8691","mycosis fungoides","mesh","D009182"
> "8691","mycosis fungoides","umls","C0026948"
> "8691","mycosis fungoides","mondo","0009691"
> "8122","pseudovascular skin squamous cell carcinoma","umls","C1335974"
> "8122","pseudovascular skin squamous cell carcinoma","mondo","0004469"
9271,9277c17653,17654
< "1933","Rubinstein-Taybi syndrome","icd10cm","Q87.2"
< "1933","Rubinstein-Taybi syndrome","mesh","D012415"
< "1933","Rubinstein-Taybi syndrome","umls","C0035934"
< "1933","Rubinstein-Taybi syndrome","mondo","0019188"
< "5577","gastrinoma","mesh","D015408"
< "5577","gastrinoma","umls","C0017150"
< "5577","gastrinoma","mondo","0003523"
---
> "7707","rectum signet ring adenocarcinoma","umls","C0279654"
> "7707","rectum signet ring adenocarcinoma","mondo","0004336"
9285,9312c17662,17663
< "0060879","primary hypomagnesemia","icd10cm","E83.4"
< "0060879","primary hypomagnesemia","mondo","0018100"
< "3093","nervous system cancer","icd9cm","192"
< "3093","nervous system cancer","icd9cm","192.9"
< "3093","nervous system cancer","mesh","D009380"
< "3093","nervous system cancer","umls","C0027665"
< "3093","nervous system cancer","umls","C0153643"
< "3093","nervous system cancer","umls","C1334956"
< "3093","nervous system cancer","mondo","0005872"
< "1243","labia minora cancer","icd10cm","C51.1"
< "1243","labia minora cancer","icd9cm","184.2"
< "1243","labia minora cancer","umls","C0496815"
< "1243","labia minora cancer","mondo","0001526"
< "10780","primary polycythemia","icd10cm","D75.0"
< "10780","primary polycythemia","icd9cm","289.6"
< "10780","primary polycythemia","mesh","C536842"
< "10780","primary polycythemia","umls","C0152264"
< "10780","primary polycythemia","mondo","0001115"
< "1245","vulva cancer","icd10cm","C51"
< "1245","vulva cancer","icd10cm","C51.9"
< "1245","vulva cancer","icd9cm","184.4"
< "1245","vulva cancer","mesh","D014846"
< "1245","vulva cancer","umls","C0042995"
< "1245","vulva cancer","umls","C0375071"
< "1245","vulva cancer","mondo","0001528"
< "1532","pleural disease","mesh","D010995"
< "1532","pleural disease","umls","C0032226"
< "1532","pleural disease","mondo","0002037"
---
> "7708","perianal skin Paget's disease","umls","C1332270"
> "7708","perianal skin Paget's disease","mondo","0004337"
9316,9326c17667,17670
< "649","prion disease","kegg","05020"
< "649","prion disease","icd10cm","A81.9"
< "649","prion disease","mesh","D017096"
< "649","prion disease","umls","C0162534"
< "649","prion disease","mondo","0005429"
< "10787","premature menopause","icd10cm","E28.31"
< "10787","premature menopause","icd10cm","E28.319"
< "10787","premature menopause","icd9cm","256.31"
< "10787","premature menopause","mesh","D008594"
< "10787","premature menopause","umls","C0025322"
< "10787","premature menopause","mondo","0001119"
---
> "0060167","seasonal affective disorder","mesh","D016574"
> "0060167","seasonal affective disorder","mondo","0000694"
> "0060165","Kleine-Levin syndrome","mesh","D017593"
> "0060165","Kleine-Levin syndrome","mondo","0007863"
9348,9430c17692,17703
< "0060614","ulnar-mammary syndrome","mesh","C536937"
< "0060614","ulnar-mammary syndrome","umls","C1866994"
< "0060614","ulnar-mammary syndrome","mondo","0008411"
< "13382","megaloblastic anemia","icd10cm","D53.1"
< "13382","megaloblastic anemia","mesh","D000749"
< "13382","megaloblastic anemia","umls","C0002888"
< "13382","megaloblastic anemia","mondo","0001700"
< "0060610","megacystis-microcolon-intestinal hypoperistalsis syndrome","mesh","C536138"
< "0060610","megacystis-microcolon-intestinal hypoperistalsis syndrome","umls","C1608393"
< "0060610","megacystis-microcolon-intestinal hypoperistalsis syndrome","mondo","0007960"
< "3267","mucinous ovarian cystadenoma","umls","C0346172"
< "3267","mucinous ovarian cystadenoma","mondo","0002583"
< "0060613","X-linked cleft palate with or without ankyloglossia","mondo","0017938"
< "332","amyotrophic lateral sclerosis","kegg","05014"
< "332","amyotrophic lateral sclerosis","icd10cm","G12.21"
< "332","amyotrophic lateral sclerosis","icd9cm","335.20"
< "332","amyotrophic lateral sclerosis","mesh","D000690"
< "332","amyotrophic lateral sclerosis","umls","C0002736"
< "332","amyotrophic lateral sclerosis","mondo","0004976"
< "0110186","Charcot-Marie-Tooth disease type 4D","icd10cm","G60.0"
< "0110186","Charcot-Marie-Tooth disease type 4D","mondo","0011085"
< "11227","acute hemorrhagic conjunctivitis","icd9cm","077.4"
< "11227","acute hemorrhagic conjunctivitis","mesh","D003232"
< "11227","acute hemorrhagic conjunctivitis","umls","C0009765"
< "11227","acute hemorrhagic conjunctivitis","mondo","0005634"
< "0060867","macrocephaly-autism syndrome","mondo","0011537"
< "12568","dyscalculia","mesh","D060705"
< "12568","dyscalculia","mondo","0001552"
< "9164","achalasia","icd10cm","K22.0"
< "9164","achalasia","icd9cm","530.0"
< "9164","achalasia","mesh","D004931"
< "9164","achalasia","umls","C0014848"
< "9164","achalasia","mondo","0008698"
< "9640","sarcocystosis","icd10cm","A07.8"
< "9640","sarcocystosis","icd9cm","136.5"
< "9640","sarcocystosis","mesh","D012523"
< "9640","sarcocystosis","umls","C0036231"
< "9640","sarcocystosis","mondo","0018903"
< "1901","vagina sarcoma","umls","C0238519"
< "1901","vagina sarcoma","mondo","0002140"
< "3892","insulinoma","mesh","D007340"
< "3892","insulinoma","mesh","D007516"
< "3892","insulinoma","umls","C0021670"
< "3892","insulinoma","umls","C0022134"
< "3892","insulinoma","mondo","0024677"
< "3896","hidradenoma","mesh","D006607"
< "3896","hidradenoma","umls","C0019522"
< "3896","hidradenoma","mondo","0002805"
< "0110489","autosomal recessive nonsyndromic deafness 30","icd10cm","H90.3"
< "0110489","autosomal recessive nonsyndromic deafness 30","mondo","0011774"
< "0060248","Simpson-Golabi-Behmel syndrome type 1","mesh","C537340"
< "0060248","Simpson-Golabi-Behmel syndrome type 1","umls","C0796154"
< "0060248","Simpson-Golabi-Behmel syndrome type 1","mondo","0020602"
< "0110520","autosomal recessive nonsyndromic deafness 7","icd10cm","H90.3"
< "0110520","autosomal recessive nonsyndromic deafness 7","mondo","0010967"
< "6612","leukocyte adhesion deficiency","mesh","D018370"
< "6612","leukocyte adhesion deficiency","umls","C0242597"
< "6612","leukocyte adhesion deficiency","mondo","0017570"
< "8955","sideroblastic anemia","icd10cm","D64.3"
< "8955","sideroblastic anemia","icd9cm","285.0"
< "8955","sideroblastic anemia","mesh","D000756"
< "8955","sideroblastic anemia","umls","C0002896"
< "8955","sideroblastic anemia","mondo","0015194"
< "2893","cervix carcinoma","umls","C0302592"
< "2893","cervix carcinoma","mondo","0005131"
< "0050799","guanidinoacetate methyltransferase deficiency","mesh","C537622"
< "0050799","guanidinoacetate methyltransferase deficiency","mondo","0012999"
< "10841","Eastern equine encephalitis","icd10cm","A83.2"
< "10841","Eastern equine encephalitis","icd9cm","062.2"
< "10841","Eastern equine encephalitis","mesh","D020242"
< "10841","Eastern equine encephalitis","umls","C0153065"
< "10841","Eastern equine encephalitis","mondo","0005736"
< "10842","Murray Valley encephalitis","icd10cm","A83.4"
< "10842","Murray Valley encephalitis","icd9cm","062.4"
< "10842","Murray Valley encephalitis","umls","C0153066"
< "10842","Murray Valley encephalitis","mondo","0001137"
< "10844","Japanese encephalitis","icd10cm","A83.0"
< "10844","Japanese encephalitis","icd9cm","062.0"
< "10844","Japanese encephalitis","mesh","D004672"
< "10844","Japanese encephalitis","umls","C0014057"
< "10844","Japanese encephalitis","mondo","0019209"
< "0110524","autosomal recessive nonsyndromic deafness 76","icd10cm","H90.3"
< "0110524","autosomal recessive nonsyndromic deafness 76","mondo","0014237"
---
> "8340","endocervical type cervical mucinous adenocarcinoma","umls","C1516421"
> "8340","endocervical type cervical mucinous adenocarcinoma","mondo","0004538"
> "4079","heart valve disease","mesh","D006349"
> "4079","heart valve disease","mesh","D016127"
> "4079","heart valve disease","umls","C0018824"
> "4079","heart valve disease","umls","C0079485"
> "4079","heart valve disease","mondo","0002869"
> "4078","tricuspid valve stenosis","mesh","D014264"
> "4078","tricuspid valve stenosis","umls","C0040963"
> "4078","tricuspid valve stenosis","mondo","0005997"
> "4075","bile duct cystadenocarcinoma","umls","C0334286"
> "4075","bile duct cystadenocarcinoma","mondo","0002868"
9438,9463c17711,17734
< "13760","Pthirus pubis infestation","icd10cm","B85.3"
< "13760","Pthirus pubis infestation","icd9cm","132.2"
< "13760","Pthirus pubis infestation","umls","C0030759"
< "13760","Pthirus pubis infestation","mondo","0001794"
< "3500","gallbladder adenocarcinoma","umls","C0279651"
< "3500","gallbladder adenocarcinoma","mondo","0006215"
< "1858","McCune Albright syndrome","icd10cm","Q78.1"
< "1858","McCune Albright syndrome","icd9cm","756.54"
< "1858","McCune Albright syndrome","mesh","D005357"
< "1858","McCune Albright syndrome","mesh","D005359"
< "1858","McCune Albright syndrome","umls","C0016063"
< "1858","McCune Albright syndrome","umls","C0016065"
< "1858","McCune Albright syndrome","mondo","0018919"
< "3962","follicular thyroid carcinoma","mesh","D018263"
< "3962","follicular thyroid carcinoma","umls","C0206682"
< "3962","follicular thyroid carcinoma","mondo","0005034"
< "5342","childhood endodermal sinus tumor","umls","C1333016"
< "5342","childhood endodermal sinus tumor","mondo","0003400"
< "5772","central nervous system hematologic cancer","umls","C1332882"
< "5772","central nervous system hematologic cancer","mondo","0003641"
< "0070197","distal myopathy 1","mondo","0008050"
< "0110483","autosomal recessive nonsyndromic deafness 25","icd10cm","H90.3"
< "0110483","autosomal recessive nonsyndromic deafness 25","mondo","0013210"
< "3969","papillary thyroid carcinoma","mesh","C536915"
< "3969","papillary thyroid carcinoma","umls","C0238463"
< "3969","papillary thyroid carcinoma","mondo","0005075"
---
> "4071","duodenogastric reflux","mesh","D004383"
> "4071","duodenogastric reflux","umls","C0013299"
> "4071","duodenogastric reflux","mondo","0006735"
> "4073","pancreatic cystadenocarcinoma","umls","C0238337"
> "4073","pancreatic cystadenocarcinoma","mondo","0002867"
> "4072","duodenum disease","mesh","D004378"
> "4072","duodenum disease","umls","C0013289"
> "4072","duodenum disease","mondo","0002866"
> "3964","trabecular follicular adenocarcinoma","umls","C0334327"
> "3964","trabecular follicular adenocarcinoma","mondo","0002821"
> "3965","Merkel cell carcinoma","umls","C0302182"
> "3965","Merkel cell carcinoma","mondo","0002822"
> "3962","thyroid gland follicular carcinoma","mesh","D018263"
> "3962","thyroid gland follicular carcinoma","umls","C0206682"
> "3962","thyroid gland follicular carcinoma","mondo","0005034"
> "3963","thyroid gland carcinoma","mesh","D013964"
> "3963","thyroid gland carcinoma","umls","C0549473"
> "3963","thyroid gland carcinoma","mondo","0015075"
> "0060751","familial temporal lobe epilepsy 7","mondo","0014639"
> "3968","papillary follicular thyroid adenocarcinoma","mesh","D018265"
> "3968","papillary follicular thyroid adenocarcinoma","umls","C0206683"
> "3968","papillary follicular thyroid adenocarcinoma","mondo","0006886"
> "5798","macrotrabecular hepatoblastoma","umls","C1334543"
> "5798","macrotrabecular hepatoblastoma","mondo","0003651"
9468,9470c17739,17743
< "0080054","achondrogenesis type IA","mondo","0008701"
< "0080055","achondrogenesis type IB","mondo","0010966"
< "0070192","autosomal recessive chronic granulomatous disease cytochrome b-positive type I","mondo","0009309"
---
> "3639","spinal cord intramedullary teratoma","umls","C1334259"
> "3639","spinal cord intramedullary teratoma","mondo","0002717"
> "0080058","autosomal recessive spinocerebellar ataxia 14","mondo","0014159"
> "3637","childhood spinal cord tumor","umls","C1134515"
> "3637","childhood spinal cord tumor","mondo","0002716"
9474,9495c17747,17751
< "0110484","autosomal recessive nonsyndromic deafness 26","icd10cm","H90.3"
< "0110484","autosomal recessive nonsyndromic deafness 26","mondo","0011553"
< "5547","pulmonary artery choriocarcinoma","umls","C1335571"
< "5547","pulmonary artery choriocarcinoma","mondo","0003506"
< "0110875","holoprosencephaly 3","mondo","0007733"
< "0110815","hereditary spastic paraplegia 64","icd10cm","G11.4"
< "0110815","hereditary spastic paraplegia 64","mondo","0014303"
< "3265","chronic granulomatous disease","icd10cm","D71"
< "3265","chronic granulomatous disease","mesh","D006105"
< "3265","chronic granulomatous disease","umls","C0018203"
< "3265","chronic granulomatous disease","mondo","0018305"
< "235","colonic benign neoplasm","mesh","D003110"
< "235","colonic benign neoplasm","umls","C0009375"
< "235","colonic benign neoplasm","mondo","0002278"
< "417","autoimmune hypersensitivity disease","icd9cm","720"
< "417","autoimmune hypersensitivity disease","umls","C0003089"
< "417","autoimmune hypersensitivity disease","mondo","0007179"
< "0070191","autosomal recessive chronic granulomatous disease cytochrome b-positive type II","mondo","0009310"
< "0050528","nonphotosensitive trichothiodystrophy","mondo","0021013"
< "0111097","Fanconi anemia complementation group J","mondo","0012187"
< "0110904","inflammatory bowel disease 8","mondo","0011699"
< "0110905","inflammatory bowel disease 22","mondo","0012886"
---
> "0060750","familial temporal lobe epilepsy 3","mondo","0012705"
> "11406","choroiditis","icd10cm","H30.9"
> "11406","choroiditis","mesh","D002833"
> "11406","choroiditis","umls","C0008526"
> "11406","choroiditis","mondo","0001280"
9499,9584c17755,17764
< "0110907","inflammatory bowel disease 6","mondo","0011700"
< "0110900","inflammatory bowel disease 2","mondo","0011087"
< "0110901","inflammatory bowel disease 26","mondo","0012973"
< "0110902","inflammatory bowel disease 27","mondo","0013012"
< "0110903","inflammatory bowel disease 4","mondo","0011701"
< "0110908","inflammatory bowel disease 24","mondo","0012940"
< "0110909","inflammatory bowel disease 25","mondo","0012941"
< "0110876","holoprosencephaly 7","mondo","0012562"
< "10939","antisocial personality disorder","icd10cm","F60.2"
< "10939","antisocial personality disorder","icd9cm","301.7"
< "10939","antisocial personality disorder","mesh","D000987"
< "10939","antisocial personality disorder","umls","C0003431"
< "10939","antisocial personality disorder","mondo","0001164"
< "0090103","Huntington's disease-like 1","icd10cm","G10"
< "0090103","Huntington's disease-like 1","mondo","0011299"
< "10935","dissociative disorder","icd10cm","F44.9"
< "10935","dissociative disorder","icd10cm","F48.9"
< "10935","dissociative disorder","icd9cm","300.15"
< "10935","dissociative disorder","icd9cm","300.9"
< "10935","dissociative disorder","mesh","D004213"
< "10935","dissociative disorder","umls","C0012746"
< "10935","dissociative disorder","umls","C0041857"
< "10935","dissociative disorder","mondo","0001160"
< "6741","bilateral breast cancer","umls","C0281267"
< "6741","bilateral breast cancer","mondo","0003982"
< "8857","lupus erythematosus","icd10cm","L93"
< "8857","lupus erythematosus","icd10cm","L93.0"
< "8857","lupus erythematosus","icd9cm","695.4"
< "8857","lupus erythematosus","umls","C0409974"
< "8857","lupus erythematosus","mondo","0004670"
< "10932","obsessive-compulsive personality disorder","icd10cm","F60.5"
< "10932","obsessive-compulsive personality disorder","icd9cm","301.4"
< "10932","obsessive-compulsive personality disorder","mesh","D003193"
< "10932","obsessive-compulsive personality disorder","umls","C0009595"
< "10932","obsessive-compulsive personality disorder","mondo","0001158"
< "10933","obsessive-compulsive disorder","icd10cm","F42"
< "10933","obsessive-compulsive disorder","icd10cm","F42.8"
< "10933","obsessive-compulsive disorder","icd10cm","F42.9"
< "10933","obsessive-compulsive disorder","icd9cm","300.3"
< "10933","obsessive-compulsive disorder","mesh","D009771"
< "10933","obsessive-compulsive disorder","umls","C0028768"
< "10933","obsessive-compulsive disorder","mondo","0008114"
< "9119","acute myeloid leukemia","kegg","05221"
< "9119","acute myeloid leukemia","icd10cm","C92.0"
< "9119","acute myeloid leukemia","icd10cm","C92.00"
< "9119","acute myeloid leukemia","icd9cm","205.0"
< "9119","acute myeloid leukemia","mesh","D015470"
< "9119","acute myeloid leukemia","umls","C0023467"
< "9119","acute myeloid leukemia","mondo","0018874"
< "11720","distal myopathy","icd10cm","G71.0"
< "11720","distal myopathy","mesh","D049310"
< "11720","distal myopathy","umls","C0751336"
< "11720","distal myopathy","mondo","0018949"
< "0070158","hereditary sensory neuropathy type 1E","icd10cm","G60.8"
< "0070158","hereditary sensory neuropathy type 1E","mondo","0013584"
< "0050554","X-linked sideroblastic anemia with ataxia","mondo","0010524"
< "0050558","Ullrich congenital muscular dystrophy","mondo","0000355"
< "0070153","hereditary sensory and autonomic neuropathy type 8","mondo","0014662"
< "0070150","hereditary sensory and autonomic neuropathy type 2B","mondo","0013142"
< "0070151","hereditary sensory and autonomic neuropathy type 6","icd10cm","G60.8"
< "0070151","hereditary sensory and autonomic neuropathy type 6","mondo","0013839"
< "0070156","hereditary sensory neuropathy type 1D","mondo","0013381"
< "0070157","hereditary sensory and autonomic neuropathy type 1C","mondo","0013337"
< "0070154","hereditary sensory neuropathy type 1F","mondo","0014286"
< "0070155","hereditary sensory and autonomic neuropathy type 2A","mondo","0024309"
< "0050790","fibular hypoplasia and complex brachydactyly","kegg","H00467"
< "0050790","fibular hypoplasia and complex brachydactyly","mesh","C537931"
< "0050790","fibular hypoplasia and complex brachydactyly","mondo","0009231"
< "3709","rectum mucinous adenocarcinoma","umls","C0279652"
< "3709","rectum mucinous adenocarcinoma","mondo","0002748"
< "0050796","achalasia microcephaly syndrome","mesh","C536010"
< "0050796","achalasia microcephaly syndrome","umls","C1860212"
< "0050796","achalasia microcephaly syndrome","mondo","0008699"
< "1319","brain cancer","icd10cm","C71"
< "1319","brain cancer","icd10cm","C71.9"
< "1319","brain cancer","icd9cm","191"
< "1319","brain cancer","icd9cm","191.9"
< "1319","brain cancer","icd9cm","239.6"
< "1319","brain cancer","mesh","D001932"
< "1319","brain cancer","umls","C0006118"
< "1319","brain cancer","umls","C0153633"
< "1319","brain cancer","umls","C0220624"
< "1319","brain cancer","umls","C0750974"
< "1319","brain cancer","umls","C0750979"
< "1319","brain cancer","umls","C1334557"
< "1319","brain cancer","mondo","0001657"
---
> "11401","xanthogranulomatous pyelonephritis","mesh","D011705"
> "11401","xanthogranulomatous pyelonephritis","umls","C0034188"
> "11401","xanthogranulomatous pyelonephritis","mondo","0007022"
> "11400","pyelonephritis","icd10cm","N10-N16"
> "11400","pyelonephritis","icd10cm","N12"
> "11400","pyelonephritis","icd10cm","N16"
> "11400","pyelonephritis","icd9cm","590.80"
> "11400","pyelonephritis","mesh","D011704"
> "11400","pyelonephritis","umls","C0034186"
> "11400","pyelonephritis","mondo","0006939"
9591,9610c17771,17788
< "0050795","cone dystrophy","mondo","0000455"
< "3702","cervical adenocarcinoma","umls","C0279672"
< "3702","cervical adenocarcinoma","mondo","0005153"
< "3703","prostate colloid adenocarcinoma","umls","C1335513"
< "3703","prostate colloid adenocarcinoma","mondo","0006067"
< "0080474","pustular psoriasis 14","icd10cm","L40.1"
< "1884","viral hepatitis","mesh","D006524"
< "1884","viral hepatitis","umls","C0019194"
< "1884","viral hepatitis","mondo","0006011"
< "1883","hepatitis C","icd10cm","B19.2"
< "1883","hepatitis C","icd10cm","B19.20"
< "1883","hepatitis C","icd9cm","070.7"
< "1883","hepatitis C","mesh","D006526"
< "1883","hepatitis C","umls","C0019196"
< "1883","hepatitis C","mondo","0005231"
< "13372","alpha 1-antitrypsin deficiency","icd10cm","E88.01"
< "13372","alpha 1-antitrypsin deficiency","icd9cm","273.4"
< "13372","alpha 1-antitrypsin deficiency","mesh","D019896"
< "13372","alpha 1-antitrypsin deficiency","umls","C0221757"
< "13372","alpha 1-antitrypsin deficiency","mondo","0013282"
---
> "13378","Kawasaki disease","icd10cm","M30.3"
> "13378","Kawasaki disease","icd9cm","446.1"
> "13378","Kawasaki disease","mesh","D009080"
> "13378","Kawasaki disease","umls","C0026691"
> "13378","Kawasaki disease","mondo","0012727"
> "4467","clear cell renal cell carcinoma","mesh","D002292"
> "4467","clear cell renal cell carcinoma","umls","C0279702"
> "4467","clear cell renal cell carcinoma","mondo","0005005"
> "4464","collecting duct carcinoma","mesh","D002292"
> "4464","collecting duct carcinoma","umls","C1266044"
> "4464","collecting duct carcinoma","mondo","0005220"
> "4465","papillary renal cell carcinoma","mesh","C538614"
> "4465","papillary renal cell carcinoma","mesh","D002292"
> "4465","papillary renal cell carcinoma","umls","C1306837"
> "4465","papillary renal cell carcinoma","umls","C1336078"
> "4465","papillary renal cell carcinoma","mondo","0017884"
> "4463","multilocular clear cell renal cell carcinoma","umls","C0346249"
> "4463","multilocular clear cell renal cell carcinoma","mondo","0003010"
9616,9633d17793
< "2340","craniosynostosis","icd10cm","Q75.0"
< "2340","craniosynostosis","mesh","D003398"
< "2340","craniosynostosis","umls","C0010278"
< "2340","craniosynostosis","mondo","0015469"
< "0110849","xeroderma pigmentosum group G","icd10cm","Q82.1"
< "0110849","xeroderma pigmentosum group G","mondo","0010216"
< "2120","focal dermal hypoplasia","mesh","D005489"
< "2120","focal dermal hypoplasia","umls","C0016395"
< "2120","focal dermal hypoplasia","mondo","0010592"
< "2122","pneumonic tularemia","icd10cm","A21.2"
< "2122","pneumonic tularemia","icd9cm","021.2"
< "2122","pneumonic tularemia","umls","C0339946"
< "2122","pneumonic tularemia","mondo","0002212"
< "13579","kwashiorkor","icd10cm","E40"
< "13579","kwashiorkor","icd9cm","260"
< "13579","kwashiorkor","mesh","D007732"
< "13579","kwashiorkor","umls","C0022806"
< "13579","kwashiorkor","mondo","0006826"
9635,9636c17795,17798
< "0090139","cortisone reductase deficiency","mesh","C536447"
< "0090139","cortisone reductase deficiency","mondo","0000193"
---
> "949","chronic dacryoadenitis","icd10cm","H04.02"
> "949","chronic dacryoadenitis","icd9cm","375.02"
> "949","chronic dacryoadenitis","umls","C0155224"
> "949","chronic dacryoadenitis","mondo","0004800"
9640,9641c17802,17803
< "0110840","Usher syndrome type 2D","icd10cm","H35.5"
< "0110840","Usher syndrome type 2D","mondo","0012662"
---
> "0090137","complex cortical dysplasia with other brain malformations 1","icd10cm","Q04.3"
> "0090137","complex cortical dysplasia with other brain malformations 1","mondo","0013541"
9644,9645c17806,17807
< "0110845","xeroderma pigmentosum group D","icd10cm","Q82.1"
< "0110845","xeroderma pigmentosum group D","mondo","0010212"
---
> "0090132","complex cortical dysplasia with other brain malformations 7","icd10cm","Q04.3"
> "0090132","complex cortical dysplasia with other brain malformations 7","mondo","0012399"
9647,9648c17809,17810
< "0110847","xeroderma pigmentosum variant type","icd10cm","Q82.1"
< "0110847","xeroderma pigmentosum variant type","mondo","0010214"
---
> "0090130","cortical dysplasia-focal epilepsy syndrome","icd10cm","Q04.8"
> "0090130","cortical dysplasia-focal epilepsy syndrome","mondo","0012400"
9650,9719d17811
< "0111082","Fanconi anemia complementation group L","mondo","0013566"
< "11712","lipoatrophic diabetes mellitus","mesh","D003923"
< "11712","lipoatrophic diabetes mellitus","umls","C0011859"
< "11712","lipoatrophic diabetes mellitus","mondo","0005827"
< "0111080","Fanconi anemia complementation group V","mondo","0014985"
< "0111081","Fanconi anemia complementation group T","mondo","0014638"
< "0111086","Fanconi anemia complementation group G","mondo","0013565"
< "0111087","Fanconi anemia complementation group C","mondo","0009213"
< "0111084","Fanconi anemia complementation group E","mondo","0010953"
< "0111085","Fanconi anemia complementation group U","mondo","0014987"
< "0111088","Fanconi anemia complementation group F","mondo","0011325"
< "0111089","Fanconi anemia complementation group D1","mondo","0011584"
< "6037","spindle cell intraocular melanoma","umls","C0279687"
< "6037","spindle cell intraocular melanoma","mondo","0003744"
< "0111017","cone-rod dystrophy 10","mondo","0012464"
< "6034","heart malignant hemangiopericytoma","umls","C1334567"
< "6034","heart malignant hemangiopericytoma","mondo","0003743"
< "2929","Newcastle disease","mesh","D009521"
< "2929","Newcastle disease","umls","C0027983"
< "2929","Newcastle disease","mondo","0005875"
< "9207","periodic limb movement disorder","icd10cm","G47.61"
< "9207","periodic limb movement disorder","icd9cm","327.51"
< "9207","periodic limb movement disorder","mesh","D020189"
< "9207","periodic limb movement disorder","umls","C0751774"
< "9207","periodic limb movement disorder","mondo","0005905"
< "2658","dermoid cyst","icd10cm","K09.8"
< "2658","dermoid cyst","mesh","D003884"
< "2658","dermoid cyst","umls","C0011649"
< "2658","dermoid cyst","mondo","0002378"
< "9201","lichen planus","icd10cm","L43"
< "9201","lichen planus","icd10cm","L43.9"
< "9201","lichen planus","icd9cm","697.0"
< "9201","lichen planus","mesh","D008010"
< "9201","lichen planus","umls","C0023646"
< "9201","lichen planus","mondo","0006572"
< "0110259","cataract 43","icd10cm","Q12.0"
< "0110259","cataract 43","mondo","0014565"
< "2349","arteriosclerosis","icd10cm","I70"
< "2349","arteriosclerosis","mesh","D001161"
< "2349","arteriosclerosis","umls","C0003850"
< "2349","arteriosclerosis","mondo","0002277"
< "133","vaginal Mullerian papilloma","umls","C1519926"
< "133","vaginal Mullerian papilloma","mondo","0001680"
< "0110592","autosomal dominant nonsyndromic deafness 70","icd10cm","H90.3"
< "0110592","autosomal dominant nonsyndromic deafness 70","mondo","0014853"
< "7388","pulmonary vein leiomyosarcoma","umls","C1335575"
< "7388","pulmonary vein leiomyosarcoma","mondo","0004206"
< "0110590","autosomal dominant nonsyndromic deafness 69","icd10cm","H90.3"
< "0110590","autosomal dominant nonsyndromic deafness 69","mondo","0014738"
< "0110597","primary ciliary dyskinesia 22","icd10cm","Q34.8"
< "0110597","primary ciliary dyskinesia 22","mondo","0014192"
< "136","vaginal carcinosarcoma","umls","C1512974"
< "136","vaginal carcinosarcoma","umls","C1519918"
< "136","vaginal carcinosarcoma","umls","C1519924"
< "136","vaginal carcinosarcoma","mondo","0006488"
< "0110595","Stromme syndrome","icd10cm","Q87.8"
< "0110595","Stromme syndrome","mondo","0009477"
< "0110594","primary ciliary dyskinesia 1","icd10cm","Q34.8"
< "0110594","primary ciliary dyskinesia 1","mondo","0009484"
< "0110599","primary ciliary dyskinesia 3","icd10cm","Q34.8"
< "0110599","primary ciliary dyskinesia 3","mondo","0012085"
< "0050175","tick-borne encephalitis","icd10cm","A84.1"
< "0050175","tick-borne encephalitis","icd9cm","063.2"
< "0050175","tick-borne encephalitis","mesh","D004675"
< "0050175","tick-borne encephalitis","umls","C0014054"
< "0050175","tick-borne encephalitis","mondo","0017572"
< "3418","glossopharyngeal nerve disease","icd10cm","G52"
< "3418","glossopharyngeal nerve disease","icd9cm","352"
< "3418","glossopharyngeal nerve disease","umls","C0154730"
< "3418","glossopharyngeal nerve disease","mondo","0002639"
9721,9722c17813
< "0110602","primary ciliary dyskinesia 11","icd10cm","Q34.8"
< "0110602","primary ciliary dyskinesia 11","mondo","0012978"
---
> "0070089","schizophrenia 13","mondo","0013089"
9735,9739c17826
< "0050486","exanthem","icd10cm","R21"
< "0050486","exanthem","icd9cm","782.1"
< "0050486","exanthem","mesh","D005076"
< "0050486","exanthem","umls","C0015230"
< "0050486","exanthem","mondo","0006547"
---
> "0070080","schizophrenia 4","mondo","0010943"
9741,9743c17828,17829
< "0110609","primary ciliary dyskinesia 23","icd10cm","Q34.8"
< "0110609","primary ciliary dyskinesia 23","mondo","0014193"
< "0050485","sennetsu fever","mondo","0000332"
---
> "0070082","schizophrenia 6","mondo","0011280"
> "0070083","schizophrenia 7","mondo","0011295"
9759,9760c17845,17848
< "10660","mediastinum neuroblastoma","umls","C1334673"
< "10660","mediastinum neuroblastoma","mondo","0001095"
---
> "12175","dyshormonogenic goiter","icd10cm","E07.1"
> "12175","dyshormonogenic goiter","icd9cm","246.1"
> "12175","dyshormonogenic goiter","umls","C0152077"
> "12175","dyshormonogenic goiter","mondo","0001460"
9763,9784c17851,17859
< "0110318","hypertrophic cardiomyopathy 12","mondo","0012804"
< "4376","milk allergy","mesh","D016269"
< "4376","milk allergy","umls","C0079840"
< "4376","milk allergy","mondo","0005849"
< "4860","brain stem astrocytic neoplasm","umls","C1332608"
< "4860","brain stem astrocytic neoplasm","mondo","0003173"
< "9682","yellow fever","icd10cm","A95"
< "9682","yellow fever","icd10cm","A95.9"
< "9682","yellow fever","icd9cm","060"
< "9682","yellow fever","icd9cm","060.9"
< "9682","yellow fever","mesh","D015004"
< "9682","yellow fever","umls","C0043395"
< "9682","yellow fever","mondo","0020502"
< "4866","salivary gland adenoid cystic carcinoma","mesh","D003528"
< "4866","salivary gland adenoid cystic carcinoma","umls","C0010606"
< "4866","salivary gland adenoid cystic carcinoma","mondo","0003175"
< "4867","cervical adenoid cystic carcinoma","umls","C1332911"
< "4867","cervical adenoid cystic carcinoma","mondo","0006133"
< "13487","childhood disintegrative disease","icd10cm","F84.3"
< "13487","childhood disintegrative disease","icd9cm","299.1"
< "13487","childhood disintegrative disease","umls","C0236791"
< "13487","childhood disintegrative disease","mondo","0001726"
---
> "12170","radial nerve lesion","icd10cm","G56.3"
> "12170","radial nerve lesion","icd10cm","G56.30"
> "12170","radial nerve lesion","icd9cm","354.3"
> "12170","radial nerve lesion","mesh","D020425"
> "12170","radial nerve lesion","umls","C0154744"
> "12170","radial nerve lesion","mondo","0006940"
> "12171","radial neuropathy","mesh","D020425"
> "12171","radial neuropathy","umls","C0748226"
> "12171","radial neuropathy","mondo","0001459"
9788,9824c17863,17874
< "9060","pityriasis versicolor","icd10cm","B36.0"
< "9060","pityriasis versicolor","icd9cm","111.0"
< "9060","pityriasis versicolor","mesh","D014010"
< "9060","pityriasis versicolor","umls","C0040262"
< "9060","pityriasis versicolor","mondo","0005915"
< "9063","Ritter's disease","icd10cm","L00"
< "9063","Ritter's disease","icd9cm","695.81"
< "9063","Ritter's disease","mesh","D013206"
< "9063","Ritter's disease","umls","C0038165"
< "9063","Ritter's disease","mondo","0005948"
< "0110028","age related macular degeneration 5","mondo","0013409"
< "0050742","nicotine dependence","icd10cm","F17"
< "0050742","nicotine dependence","icd10cm","F17.2"
< "0050742","nicotine dependence","icd10cm","F17.20"
< "0050742","nicotine dependence","mesh","D014029"
< "0050742","nicotine dependence","umls","C0028043"
< "0050742","nicotine dependence","mondo","0008575"
< "0110023","age related macular degeneration 11","mondo","0012767"
< "0110022","age related macular degeneration 10","mondo","0012674"
< "0110021","age related macular degeneration 9","mondo","0012659"
< "0110020","age related macular degeneration 8","mondo","0013416"
< "0110027","age related macular degeneration 15","mondo","0014266"
< "0110026","age related macular degeneration 14","mondo","0014207"
< "0110025","age related macular degeneration 13","mondo","0014189"
< "0110024","age related macular degeneration 12","mondo","0013420"
< "9667","placental abruption","icd10cm","O20.0"
< "9667","placental abruption","icd9cm","640.0"
< "9667","placental abruption","icd9cm","640.03"
< "9667","placental abruption","mesh","D000033"
< "9667","placental abruption","mesh","D000037"
< "9667","placental abruption","umls","C0000821"
< "9667","placental abruption","mondo","0004846"
< "10934","multiple personality disorder","icd10cm","F44.81"
< "10934","multiple personality disorder","icd9cm","300.14"
< "10934","multiple personality disorder","mesh","D009105"
< "10934","multiple personality disorder","umls","C0026773"
< "10934","multiple personality disorder","mondo","0001159"
---
> "0111514","metatropic dysplasia","mesh","C537356"
> "0111514","metatropic dysplasia","umls","C0265281"
> "0111510","Marshall syndrome","mesh","C536025"
> "0111510","Marshall syndrome","umls","C0265235"
> "0111511","melanoma and neural system tumor syndrome","mesh","C536149"
> "0111511","melanoma and neural system tumor syndrome","umls","C1835042"
> "0111512","metachondromatosis","mesh","C562938"
> "0111512","metachondromatosis","umls","C0410530"
> "6457","Cowden syndrome","mesh","D006223"
> "6457","Cowden syndrome","umls","C0018553"
> "6457","Cowden syndrome","umls","C0391826"
> "6457","Cowden syndrome","mondo","0016063"
9831,9838c17881,17888
< "0040028","succinylcholine allergy","umls","C0571140"
< "0040025","cefuroxime allergy","umls","C0571454"
< "0040024","ceftazidime allergy","umls","C0571458"
< "0040027","cyclophosphamide allergy","umls","C0570670"
< "2926","Klippel-Trenaunay syndrome","icd10cm","Q87.2"
< "2926","Klippel-Trenaunay syndrome","mesh","D007715"
< "2926","Klippel-Trenaunay syndrome","umls","C0022739"
< "2926","Klippel-Trenaunay syndrome","mondo","0007864"
---
> "10444","ring corneal ulcer","icd10cm","H16.02"
> "10444","ring corneal ulcer","icd9cm","370.02"
> "10444","ring corneal ulcer","umls","C0155068"
> "10444","ring corneal ulcer","mondo","0001037"
> "10445","perforated corneal ulcer","icd10cm","H16.07"
> "10445","perforated corneal ulcer","icd9cm","370.06"
> "10445","perforated corneal ulcer","umls","C0151844"
> "10445","perforated corneal ulcer","mondo","0001038"
9846,9881c17896,17910
< "0040023","cefaclor allergy","umls","C0571453"
< "0040022","amodiaquine allergy","umls","C0571303"
< "3565","meningioma","icd10cm","D32.9"
< "3565","meningioma","mesh","D008577"
< "3565","meningioma","mesh","D008579"
< "3565","meningioma","umls","C0025284"
< "3565","meningioma","umls","C0025286"
< "3565","meningioma","umls","C0349604"
< "3565","meningioma","umls","C1334698"
< "3565","meningioma","umls","C1336537"
< "3565","meningioma","mondo","0016642"
< "13159","scrotum squamous cell carcinoma","umls","C0349551"
< "13159","scrotum squamous cell carcinoma","mondo","0001651"
< "13198","endemic goiter","icd10cm","E01.0"
< "13198","endemic goiter","icd10cm","E01.2"
< "13198","endemic goiter","icd9cm","240.0"
< "13198","endemic goiter","mesh","D006043"
< "13198","endemic goiter","umls","C0018022"
< "13198","endemic goiter","mondo","0006742"
< "10591","pre-eclampsia","icd10cm","O14"
< "10591","pre-eclampsia","icd10cm","O14.9"
< "10591","pre-eclampsia","icd10cm","O14.90"
< "10591","pre-eclampsia","mesh","D011225"
< "10591","pre-eclampsia","umls","C0032914"
< "10591","pre-eclampsia","mondo","0005081"
< "4480","achondroplasia","icd10cm","Q77.4"
< "4480","achondroplasia","mesh","D000130"
< "4480","achondroplasia","umls","C0001080"
< "4480","achondroplasia","mondo","0007037"
< "4481","allergic rhinitis","mesh","D065631"
< "4481","allergic rhinitis","umls","C0002103"
< "4481","allergic rhinitis","mondo","0011786"
< "0110119","autoimmune lymphoproliferative syndrome type 3","icd10cm","D47.9"
< "0110119","autoimmune lymphoproliferative syndrome type 3","mondo","0014253"
< "0110118","Leber congenital amaurosis 16","icd10cm","H35.5"
< "0110118","Leber congenital amaurosis 16","mondo","0013613"
---
> "10113","trypanosomiasis","icd10cm","B57.2"
> "10113","trypanosomiasis","icd9cm","086"
> "10113","trypanosomiasis","icd9cm","086.9"
> "10113","trypanosomiasis","mesh","D014352"
> "10113","trypanosomiasis","umls","C0041227"
> "10113","trypanosomiasis","mondo","0000940"
> "9669","senile cataract","icd10cm","H25"
> "9669","senile cataract","icd9cm","366.1"
> "9669","senile cataract","icd9cm","366.10"
> "9669","senile cataract","umls","C0036646"
> "9669","senile cataract","mondo","0004847"
> "10443","hypopyon","icd10cm","H20.05"
> "10443","hypopyon","icd9cm","364.05"
> "10443","hypopyon","umls","C0020641"
> "10443","hypopyon","mondo","0001036"
9887,9962c17916,17930
< "0110116","autoimmune lymphoproliferative syndrome type 2B","icd10cm","D47.9"
< "0110116","autoimmune lymphoproliferative syndrome type 2B","mondo","0011804"
< "0110115","autoimmune lymphoproliferative syndrome type 2A","icd10cm","D47.9"
< "0110115","autoimmune lymphoproliferative syndrome type 2A","mondo","0011383"
< "0110114","atrial heart septal defect 9","icd10cm","Q21.1"
< "0110114","atrial heart septal defect 9","mondo","0013770"
< "13399","color blindness","icd10cm","H53.5"
< "13399","color blindness","icd10cm","H53.50"
< "13399","color blindness","icd9cm","368.5"
< "13399","color blindness","mesh","D003117"
< "13399","color blindness","umls","C0242225"
< "13399","color blindness","mondo","0001703"
< "0110112","atrial heart septal defect 7","icd10cm","Q21.1"
< "0110112","atrial heart septal defect 7","mondo","0007173"
< "0110111","atrial heart septal defect 6","icd10cm","Q21.1"
< "0110111","atrial heart septal defect 6","mondo","0013123"
< "0110110","atrial heart septal defect 5","icd10cm","Q21.1"
< "0110110","atrial heart septal defect 5","mondo","0013011"
< "0110337","osteogenesis imperfecta type 7","icd10cm","Q78.0"
< "0110337","osteogenesis imperfecta type 7","mondo","0012536"
< "0110336","osteogenesis imperfecta type 8","icd10cm","Q78.0"
< "0110336","osteogenesis imperfecta type 8","mondo","0012581"
< "6857","pineal region mature teratoma","umls","C1335417"
< "6857","pineal region mature teratoma","mondo","0004016"
< "0110334","osteogenesis imperfecta type 1","icd10cm","Q78.0"
< "0110334","osteogenesis imperfecta type 1","mondo","0008146"
< "0110333","Leber congenital amaurosis 7","icd10cm","H35.5"
< "0110333","Leber congenital amaurosis 7","mondo","0013449"
< "0110332","Leber congenital amaurosis 4","icd10cm","H35.5"
< "0110332","Leber congenital amaurosis 4","mondo","0011458"
< "0110331","Leber congenital amaurosis 3","icd10cm","H35.5"
< "0110331","Leber congenital amaurosis 3","mondo","0011415"
< "0110330","Leber congenital amaurosis 13","icd10cm","H35.5"
< "0110330","Leber congenital amaurosis 13","mondo","0012990"
< "707","B-cell lymphoma","mesh","D016393"
< "707","B-cell lymphoma","umls","C0079731"
< "707","B-cell lymphoma","mondo","0004095"
< "701","dentin dysplasia","icd10cm","K00.5"
< "701","dentin dysplasia","mesh","D003805"
< "701","dentin dysplasia","umls","C0011430"
< "701","dentin dysplasia","mondo","0015613"
< "0110339","osteogenesis imperfecta type 3","icd10cm","Q78.0"
< "0110339","osteogenesis imperfecta type 3","mondo","0009804"
< "0110525","autosomal recessive nonsyndromic deafness 77","icd10cm","H90.3"
< "0110525","autosomal recessive nonsyndromic deafness 77","mondo","0013119"
< "0050819","Matthew-Wood syndrome","mondo","0011010"
< "0050818","transcobalamin II deficiency","mondo","0010149"
< "0050814","temtamy preaxial brachydactyly syndrome","mondo","0011533"
< "11889","female breast nipple and areola cancer","icd9cm","174.0"
< "11889","female breast nipple and areola cancer","umls","C0024621"
< "11889","female breast nipple and areola cancer","mondo","0001401"
< "0050816","urofacial syndrome","mesh","C536480"
< "0050816","urofacial syndrome","mondo","0000463"
< "0050811","congenital adrenal hyperplasia","icd10cm","E25"
< "0050811","congenital adrenal hyperplasia","icd10cm","E25.9"
< "0050811","congenital adrenal hyperplasia","icd9cm","255.2"
< "0050811","congenital adrenal hyperplasia","umls","C0701163"
< "0050811","congenital adrenal hyperplasia","mondo","0018479"
< "0050810","biotin deficiency","mesh","C531633"
< "0050810","biotin deficiency","mondo","0000461"
< "0050813","spondyloepiphyseal dysplasia with congenital joint dislocations","mondo","0007738"
< "0050812","spondyloepimetaphyseal dysplasia, Pakistani type","mondo","0013019"
< "0050637","Finnish type amyloidosis","mondo","0007097"
< "0070152","hereditary sensory and autonomic neuropathy type 1A","mondo","0008086"
< "1659","supratentorial cancer","icd10cm","C71.0"
< "1659","supratentorial cancer","mesh","D015173"
< "1659","supratentorial cancer","umls","C0038874"
< "1659","supratentorial cancer","umls","C0751589"
< "1659","supratentorial cancer","mondo","0002071"
< "0050419","complement factor I deficiency","mesh","C572568"
< "0050419","complement factor I deficiency","mondo","0012594"
< "0070089","schizophrenia 13","mondo","0013089"
< "8802","trachea carcinoma in situ","icd10cm","D02.1"
< "8802","trachea carcinoma in situ","icd9cm","231.1"
< "8802","trachea carcinoma in situ","umls","C0154070"
< "8802","trachea carcinoma in situ","mondo","0004661"
---
> "7139","endometrial small cell carcinoma","umls","C1516858"
> "7139","endometrial small cell carcinoma","mondo","0006197"
> "7138","cystitis cystica","icd9cm","595.81"
> "7138","cystitis cystica","umls","C0152262"
> "7138","cystitis cystica","mondo","0004118"
> "7133","gallbladder small cell carcinoma","umls","C1333759"
> "7133","gallbladder small cell carcinoma","mondo","0006219"
> "7132","urinary bladder small cell neuroendocrine carcinoma","umls","C1332564"
> "7132","urinary bladder small cell neuroendocrine carcinoma","mondo","0004114"
> "7134","esophagus small cell carcinoma","umls","C1112474"
> "7134","esophagus small cell carcinoma","mondo","0004116"
> "7136","ampulla of Vater small cell carcinoma","umls","C1332250"
> "7136","ampulla of Vater small cell carcinoma","mondo","0004117"
> "7684","maxillary sinus adenocarcinoma","umls","C1334642"
> "7684","maxillary sinus adenocarcinoma","mondo","0004328"
9972,10012c17940,17983
< "0060289","Ohdo syndrome","mesh","C536232"
< "0060289","Ohdo syndrome","umls","C0796094"
< "0060289","Ohdo syndrome","mondo","0000734"
< "6587","invasive tubular breast carcinoma","umls","C1328544"
< "6587","invasive tubular breast carcinoma","mondo","0003936"
< "0060281","photosensitive epilepsy","icd10cm","G40.8"
< "0060281","photosensitive epilepsy","mondo","0015643"
< "0060287","cornea plana","icd10cm","Q13.4"
< "0060287","cornea plana","mondo","0000733"
< "8200","tertiary syphilis","icd10cm","A52"
< "8200","tertiary syphilis","icd10cm","A52.3"
< "8200","tertiary syphilis","icd10cm","A52.9"
< "8200","tertiary syphilis","icd9cm","097.0"
< "8200","tertiary syphilis","mesh","C536774"
< "8200","tertiary syphilis","umls","C0153188"
< "8200","tertiary syphilis","mondo","0004497"
< "9442","cervical Mullerian papilloma","umls","C1516427"
< "9442","cervical Mullerian papilloma","mondo","0004787"
< "0060063","sideroblastic anemia 1","mondo","0010419"
< "3151","skin squamous cell carcinoma","umls","C0553723"
< "3151","skin squamous cell carcinoma","mondo","0002529"
< "3156","hypomelanosis of Ito","mesh","D010859"
< "3156","hypomelanosis of Ito","umls","C0022283"
< "3156","hypomelanosis of Ito","mondo","0010302"
< "3210","Pelizaeus-Merzbacher disease","mesh","D020371"
< "3210","Pelizaeus-Merzbacher disease","umls","C0205711"
< "3210","Pelizaeus-Merzbacher disease","mondo","0010714"
< "11080","myiasis","icd10cm","B87"
< "11080","myiasis","icd10cm","B87.9"
< "11080","myiasis","icd9cm","134.0"
< "11080","myiasis","mesh","D009198"
< "11080","myiasis","umls","C0027030"
< "11080","myiasis","mondo","0019147"
< "1386","abetalipoproteinemia","icd10cm","E78.6"
< "1386","abetalipoproteinemia","mesh","D000012"
< "1386","abetalipoproteinemia","umls","C0000744"
< "1386","abetalipoproteinemia","mondo","0008692"
< "3390","palmoplantar keratosis","icd10cm","L85.2"
< "3390","palmoplantar keratosis","mesh","D007645"
< "3390","palmoplantar keratosis","umls","C0022596"
< "3390","palmoplantar keratosis","mondo","0006590"
---
> "585","nephrolithiasis","icd10cm","N20"
> "585","nephrolithiasis","icd10cm","N20.2"
> "585","nephrolithiasis","icd9cm","592"
> "585","nephrolithiasis","mesh","D053040"
> "585","nephrolithiasis","umls","C0156257"
> "585","nephrolithiasis","mondo","0008171"
> "582","hemoglobinuria","icd10cm","R82.3"
> "582","hemoglobinuria","icd9cm","791.2"
> "582","hemoglobinuria","mesh","D006456"
> "582","hemoglobinuria","umls","C0019048"
> "582","hemoglobinuria","mondo","0003656"
> "583","hemolytic anemia","icd10cm","D55-D59"
> "583","hemolytic anemia","mesh","D000743"
> "583","hemolytic anemia","umls","C0002878"
> "583","hemolytic anemia","mondo","0003664"
> "580","acute urate nephropathy","icd9cm","274.11"
> "580","acute urate nephropathy","umls","C0403719"
> "580","acute urate nephropathy","mondo","0003652"
> "589","congenital hemolytic anemia","icd10cm","D58.9"
> "589","congenital hemolytic anemia","icd9cm","282"
> "589","congenital hemolytic anemia","icd9cm","282.9"
> "589","congenital hemolytic anemia","mesh","D000745"
> "589","congenital hemolytic anemia","umls","C0002881"
> "589","congenital hemolytic anemia","mondo","0003689"
> "2839","erythropoietin polycythemia","icd10cm","D75.1"
> "2839","erythropoietin polycythemia","umls","C0391869"
> "2839","erythropoietin polycythemia","mondo","0002440"
> "2838","stress polycythemia","icd10cm","D75.1"
> "2838","stress polycythemia","umls","C0541719"
> "2838","stress polycythemia","mondo","0019538"
> "2835","polycythemia due to hypoxia","umls","C0856818"
> "2835","polycythemia due to hypoxia","mondo","0005572"
> "2834","acquired polycythemia","icd10cm","D75.1"
> "2834","acquired polycythemia","icd9cm","289.0"
> "2834","acquired polycythemia","umls","C1318533"
> "2834","acquired polycythemia","mondo","0002438"
> "2833","dehydration polycythemia","umls","C0856815"
> "2833","dehydration polycythemia","mondo","0002437"
> "2832","geotrichosis","icd10cm","B48.3"
> "2832","geotrichosis","mesh","D005847"
> "2832","geotrichosis","umls","C0017455"
> "2832","geotrichosis","mondo","0005772"
> "0050969","spinocerebellar ataxia type 18","mondo","0011834"
> "0050968","autosomal dominant cerebellar ataxia, deafness and narcolepsy","mondo","0011397"
10030,10036c18001,18005
< "1432","blindness","icd10cm","H54"
< "1432","blindness","icd9cm","369"
< "1432","blindness","mesh","D001766"
< "1432","blindness","umls","C0155020"
< "1432","blindness","mondo","0001941"
< "0060578","Noonan syndrome 1","icd10cm","Q87.1"
< "0060578","Noonan syndrome 1","mondo","0008104"
---
> "5403","microcystic adenoma","mesh","D000236"
> "5403","microcystic adenoma","umls","C0205648"
> "5403","microcystic adenoma","mondo","0003435"
> "5402","vaginal adenoma","umls","C1519913"
> "5402","vaginal adenoma","mondo","0003434"
10039,10044c18008,18011
< "0060574","von Willebrand's disease 2","mesh","D056728"
< "0060574","von Willebrand's disease 2","umls","C1264040"
< "0060574","von Willebrand's disease 2","mondo","0013304"
< "14723","beta-ketothiolase deficiency","mesh","C535818"
< "14723","beta-ketothiolase deficiency","umls","C1533628"
< "14723","beta-ketothiolase deficiency","mondo","0008760"
---
> "0050961","spinocerebellar ataxia type 11","mondo","0011464"
> "0050960","spinocerebellar ataxia type 10","mondo","0011330"
> "0050963","spinocerebellar ataxia type 13","mondo","0011529"
> "0050962","spinocerebellar ataxia type 12","mondo","0011439"
10046,10101c18013,18035
< "0060573","von Willebrand's disease 1","mesh","D056725"
< "0060573","von Willebrand's disease 1","umls","C1264039"
< "0060573","von Willebrand's disease 1","mondo","0008668"
< "419","scleroderma","mesh","D012594"
< "419","scleroderma","umls","C0011644"
< "419","scleroderma","mondo","0019340"
< "0050791","persistent Mullerian duct syndrome","mesh","C536665"
< "0050791","persistent Mullerian duct syndrome","umls","C1849930"
< "0050791","persistent Mullerian duct syndrome","mondo","0009857"
< "0060065","autosomal recessive pyridoxine-refractory sideroblastic anemia 2","mondo","0008785"
< "2789","parasitic protozoa infectious disease","icd10cm","B50-B64"
< "2789","parasitic protozoa infectious disease","icd10cm","B64"
< "2789","parasitic protozoa infectious disease","mesh","D011528"
< "2789","parasitic protozoa infectious disease","umls","C0033740"
< "2789","parasitic protozoa infectious disease","mondo","0002428"
< "2841","asthma","kegg","05310"
< "2841","asthma","icd10cm","J45"
< "2841","asthma","icd10cm","J45.90"
< "2841","asthma","icd10cm","J45.909"
< "2841","asthma","icd9cm","493"
< "2841","asthma","icd9cm","493.9"
< "2841","asthma","mesh","D001249"
< "2841","asthma","umls","C0004096"
< "2841","asthma","mondo","0004979"
< "0060376","Joubert syndrome with orofaciodigital defect","mesh","C536531"
< "0060376","Joubert syndrome with orofaciodigital defect","umls","C2745997"
< "0060376","Joubert syndrome with orofaciodigital defect","mondo","0010176"
< "0060375","orofaciodigital syndrome V","mesh","C557819"
< "0060375","orofaciodigital syndrome V","umls","C1868118"
< "0060375","orofaciodigital syndrome V","mondo","0008267"
< "0060374","orofaciodigital syndrome IV","mesh","C537133"
< "0060374","orofaciodigital syndrome IV","umls","C0406727"
< "0060374","orofaciodigital syndrome IV","mondo","0009794"
< "0060373","orofaciodigital syndrome III","mesh","C557817"
< "0060373","orofaciodigital syndrome III","umls","C0406726"
< "0060373","orofaciodigital syndrome III","mondo","0009793"
< "0060372","autosomal recessive early-onset Parkinson's disease 15","mondo","0009830"
< "0060371","autosomal dominant Parkinson's disease 8","mondo","0011764"
< "0050797","peroxisomal acyl-CoA oxidase deficiency","mesh","C536662"
< "0050797","peroxisomal acyl-CoA oxidase deficiency","umls","C1849678"
< "0050797","peroxisomal acyl-CoA oxidase deficiency","mondo","0009919"
< "0060597","atypical chronic myeloid leukemia","icd10cm","C92.2"
< "0060597","atypical chronic myeloid leukemia","icd10cm","C92.20"
< "0060597","atypical chronic myeloid leukemia","mesh","D054438"
< "0060597","atypical chronic myeloid leukemia","umls","C1292772"
< "0060597","atypical chronic myeloid leukemia","mondo","0020312"
< "13972","female breast lower-outer quadrant cancer","icd10cm","C50.51"
< "13972","female breast lower-outer quadrant cancer","icd9cm","174.5"
< "13972","female breast lower-outer quadrant cancer","umls","C0153553"
< "13972","female breast lower-outer quadrant cancer","mondo","0001850"
< "4265","angiomyoma","mesh","D018229"
< "4265","angiomyoma","umls","C0206653"
< "4265","angiomyoma","mondo","0006646"
< "0060591","WHIM syndrome","mesh","C536697"
< "0060591","WHIM syndrome","umls","C0472817"
< "0060591","WHIM syndrome","mondo","0008674"
---
> "0050964","spinocerebellar ataxia type 14","mondo","0011540"
> "0050967","spinocerebellar ataxia type 17","mondo","0011781"
> "5408","Paget's disease of bone","icd10cm","M88"
> "5408","Paget's disease of bone","mesh","D010001"
> "5408","Paget's disease of bone","umls","C0029401"
> "5408","Paget's disease of bone","mondo","0005382"
> "1731","histoplasmosis","icd10cm","B39"
> "1731","histoplasmosis","icd10cm","B39.9"
> "1731","histoplasmosis","icd9cm","115"
> "1731","histoplasmosis","icd9cm","115.9"
> "1731","histoplasmosis","mesh","C538362"
> "1731","histoplasmosis","mesh","D006660"
> "1731","histoplasmosis","umls","C0019655"
> "1731","histoplasmosis","umls","C0035288"
> "1731","histoplasmosis","mondo","0018312"
> "0040056","chromium allergic contact dermatitis","icd10cm","L23.0"
> "4260","gait apraxia","mesh","D020235"
> "4260","gait apraxia","umls","C1510417"
> "4260","gait apraxia","mondo","0006766"
> "0040057","benzoic acid allergic contact dermatitis","umls","C0571102"
> "0060592","B-cell adult acute lymphocytic leukemia","mondo","0000814"
> "4266","intravascular angioleiomyoma","umls","C1334267"
> "4266","intravascular angioleiomyoma","mondo","0002934"
10104,10149c18038,18052
< "452","pleomorphic adenoma","mesh","D008949"
< "452","pleomorphic adenoma","umls","C0026277"
< "452","pleomorphic adenoma","mondo","0008401"
< "13378","Kawasaki disease","icd10cm","M30.3"
< "13378","Kawasaki disease","icd9cm","446.1"
< "13378","Kawasaki disease","mesh","D009080"
< "13378","Kawasaki disease","umls","C0026691"
< "13378","Kawasaki disease","mondo","0012727"
< "456","ascariasis","icd10cm","B77"
< "456","ascariasis","icd10cm","B77.9"
< "456","ascariasis","icd9cm","127.0"
< "456","ascariasis","mesh","D001196"
< "456","ascariasis","umls","C0003950"
< "456","ascariasis","mondo","0005654"
< "8118","mature gastric teratoma","umls","C1334635"
< "8118","mature gastric teratoma","mondo","0004467"
< "4467","clear cell renal cell carcinoma","mesh","D002292"
< "4467","clear cell renal cell carcinoma","umls","C0279702"
< "4467","clear cell renal cell carcinoma","mondo","0005005"
< "4464","collecting duct carcinoma","mesh","D002292"
< "4464","collecting duct carcinoma","umls","C1266044"
< "4464","collecting duct carcinoma","mondo","0005220"
< "9870","galactosemia","icd10cm","E74.21"
< "9870","galactosemia","icd9cm","271.1"
< "9870","galactosemia","mesh","D005693"
< "9870","galactosemia","umls","C0016952"
< "9870","galactosemia","mondo","0018116"
< "11155","hypohidrosis","icd10cm","L74.4"
< "11155","hypohidrosis","mesh","D007007"
< "11155","hypohidrosis","umls","C0020620"
< "11155","hypohidrosis","mondo","0006560"
< "0110005","Leber congenital amaurosis 9","icd10cm","H35.5"
< "0110005","Leber congenital amaurosis 9","mondo","0012056"
< "13374","fibrodysplasia ossificans progressiva","icd10cm","M61.1"
< "13374","fibrodysplasia ossificans progressiva","icd10cm","M61.10"
< "13374","fibrodysplasia ossificans progressiva","icd9cm","728.11"
< "13374","fibrodysplasia ossificans progressiva","mesh","D009221"
< "13374","fibrodysplasia ossificans progressiva","umls","C0016037"
< "13374","fibrodysplasia ossificans progressiva","mondo","0007606"
< "11153","miliaria rubra","icd10cm","L74.0"
< "11153","miliaria rubra","icd9cm","705.1"
< "11153","miliaria rubra","mesh","D008883"
< "11153","miliaria rubra","umls","C0162423"
< "11153","miliaria rubra","mondo","0006581"
< "0110556","autosomal dominant nonsyndromic deafness 27","icd10cm","H90.3"
< "0110556","autosomal dominant nonsyndromic deafness 27","mondo","0012902"
---
> "0060599","Nance-Horan syndrome","mesh","C538336"
> "0060599","Nance-Horan syndrome","umls","C0796085"
> "0060599","Nance-Horan syndrome","mondo","0010545"
> "3702","cervical adenocarcinoma","umls","C0279672"
> "3702","cervical adenocarcinoma","mondo","0005153"
> "1737","duodenal benign neoplasm","mesh","D004379"
> "1737","duodenal benign neoplasm","umls","C0013291"
> "1737","duodenal benign neoplasm","mondo","0006734"
> "3700","uterine ligament adenocarcinoma","umls","C1519866"
> "3700","uterine ligament adenocarcinoma","mondo","0002741"
> "3701","cervical mucinous adenocarcinoma","umls","C1332919"
> "3701","cervical mucinous adenocarcinoma","mondo","0002742"
> "0060731","congenital central hypoventilation syndrome","icd10cm","G47.3"
> "0060731","congenital central hypoventilation syndrome","mesh","C536209"
> "0060731","congenital central hypoventilation syndrome","mondo","0008852"
10157,10175c18060,18065
< "0110555","autosomal dominant nonsyndromic deafness 25","icd10cm","H90.3"
< "0110555","autosomal dominant nonsyndromic deafness 25","mondo","0011568"
< "13431","bejel","mesh","D014211"
< "13431","bejel","umls","C0004945"
< "13431","bejel","mondo","0001714"
< "656","adrenal adenoma","mondo","0003924"
< "657","adenoma","mesh","D000236"
< "657","adenoma","umls","C0001430"
< "657","adenoma","umls","C0334389"
< "657","adenoma","mondo","0004972"
< "0060119","pharynx cancer","mesh","D010610"
< "0060119","pharynx cancer","umls","C0031347"
< "0060119","pharynx cancer","mondo","0005517"
< "0110554","autosomal dominant nonsyndromic deafness 24","icd10cm","H90.3"
< "0110554","autosomal dominant nonsyndromic deafness 24","mondo","0011657"
< "653","purine-pyrimidine metabolic disorder","icd10cm","E79.8"
< "653","purine-pyrimidine metabolic disorder","icd9cm","277.2"
< "653","purine-pyrimidine metabolic disorder","umls","C0029595"
< "653","purine-pyrimidine metabolic disorder","mondo","0019254"
---
> "5547","pulmonary artery choriocarcinoma","umls","C1335571"
> "5547","pulmonary artery choriocarcinoma","mondo","0003506"
> "5545","anal neuroendocrine tumor","umls","C1332273"
> "5545","anal neuroendocrine tumor","mondo","0003504"
> "3704","fallopian tube mucinous adenocarcinoma","umls","C1517119"
> "3704","fallopian tube mucinous adenocarcinoma","mondo","0002744"
10184,10211c18074,18093
< "0110001","3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","mondo","0013875"
< "1508","candidiasis","icd10cm","B37"
< "1508","candidiasis","icd10cm","B37.9"
< "1508","candidiasis","icd9cm","112"
< "1508","candidiasis","icd9cm","112.9"
< "1508","candidiasis","mesh","D002177"
< "1508","candidiasis","umls","C0006840"
< "1508","candidiasis","mondo","0002026"
< "1509","avoidant personality disorder","icd10cm","F60.6"
< "1509","avoidant personality disorder","icd9cm","301.82"
< "1509","avoidant personality disorder","mesh","D010554"
< "1509","avoidant personality disorder","umls","C0004444"
< "1509","avoidant personality disorder","mondo","0002027"
< "0110552","autosomal dominant nonsyndromic deafness 22","icd10cm","H90.3"
< "0110552","autosomal dominant nonsyndromic deafness 22","mondo","0011660"
< "3429","inclusion body myositis","icd10cm","G72.41"
< "3429","inclusion body myositis","icd9cm","359.71"
< "3429","inclusion body myositis","mesh","D018979"
< "3429","inclusion body myositis","umls","C0238190"
< "3429","inclusion body myositis","mondo","0007827"
< "4656","extraocular retinoblastoma","umls","C0278719"
< "4656","extraocular retinoblastoma","mondo","0003078"
< "0110551","autosomal dominant nonsyndromic deafness 21","icd10cm","H90.3"
< "0110551","autosomal dominant nonsyndromic deafness 21","mondo","0011761"
< "0110848","xeroderma pigmentosum group F","icd10cm","Q82.1"
< "0110848","xeroderma pigmentosum group F","mondo","0010215"
< "0110550","autosomal dominant nonsyndromic deafness 20","icd10cm","H90.3"
< "0110550","autosomal dominant nonsyndromic deafness 20","mondo","0011480"
---
> "8593","chronic monocytic leukemia","icd10cm","C93.1"
> "8593","chronic monocytic leukemia","icd9cm","206.1"
> "8593","chronic monocytic leukemia","mesh","D007951"
> "8593","chronic monocytic leukemia","umls","C0023466"
> "8593","chronic monocytic leukemia","mondo","0004614"
> "8590","acute vascular insufficiency of intestine","icd9cm","557.0"
> "8590","acute vascular insufficiency of intestine","umls","C0001363"
> "8590","acute vascular insufficiency of intestine","mondo","0004613"
> "0110590","autosomal dominant nonsyndromic deafness 69","icd10cm","H90.3"
> "0110590","autosomal dominant nonsyndromic deafness 69","mondo","0014738"
> "0060730","torsion dystonia 1","icd10cm","G24.1"
> "0060730","torsion dystonia 1","mondo","0007492"
> "11812","bladder sarcoma","umls","C0349666"
> "11812","bladder sarcoma","mondo","0001374"
> "11813","bladder trigone cancer","icd10cm","C67.0"
> "11813","bladder trigone cancer","icd9cm","188.0"
> "11813","bladder trigone cancer","umls","C0496826"
> "11813","bladder trigone cancer","mondo","0001375"
> "5890","malignant adult ependymoma","umls","C0280787"
> "5890","malignant adult ependymoma","mondo","0003690"
10217,10226c18099,18102
< "0070177","spermatogenic failure 22","mondo","0054726"
< "8577","ulcerative colitis","icd10cm","K51"
< "8577","ulcerative colitis","icd10cm","K51.9"
< "8577","ulcerative colitis","icd9cm","556"
< "8577","ulcerative colitis","icd9cm","556.5"
< "8577","ulcerative colitis","icd9cm","556.9"
< "8577","ulcerative colitis","mesh","D003093"
< "8577","ulcerative colitis","umls","C0009324"
< "8577","ulcerative colitis","umls","C0375359"
< "8577","ulcerative colitis","mondo","0005101"
---
> "5893","childhood malignant mesenchymoma","umls","C0279991"
> "5893","childhood malignant mesenchymoma","mondo","0003691"
> "5894","adult malignant mesenchymoma","umls","C0279548"
> "5894","adult malignant mesenchymoma","mondo","0003692"
10229,10230c18105,18122
< "5684","spondyloepimetaphyseal dysplasia, Sponastrime type","umls","C0920349"
< "5684","spondyloepimetaphyseal dysplasia, Sponastrime type","mondo","0010068"
---
> "5896","ovarian clear cell cystadenofibroma","umls","C1518695"
> "5896","ovarian clear cell cystadenofibroma","mondo","0003694"
> "5897","ovarian clear cell adenofibroma","umls","C1518694"
> "5897","ovarian clear cell adenofibroma","mondo","0003695"
> "11230","acute orbital inflammation","icd10cm","H05.0"
> "11230","acute orbital inflammation","icd10cm","H05.00"
> "11230","acute orbital inflammation","icd9cm","376.0"
> "11230","acute orbital inflammation","icd9cm","376.00"
> "11230","acute orbital inflammation","umls","C0155256"
> "11230","acute orbital inflammation","mondo","0001230"
> "11231","orbital periostitis","icd10cm","H05.03"
> "11231","orbital periostitis","icd9cm","376.02"
> "11231","orbital periostitis","umls","C0155257"
> "11231","orbital periostitis","mondo","0001231"
> "11232","orbital osteomyelitis","icd10cm","H05.02"
> "11232","orbital osteomyelitis","icd9cm","376.03"
> "11232","orbital osteomyelitis","umls","C0155258"
> "11232","orbital osteomyelitis","mondo","0001232"
10234,10257c18126,18141
< "13801","pharyngoconjunctival fever","icd9cm","077.2"
< "13801","pharyngoconjunctival fever","mesh","D000258"
< "13801","pharyngoconjunctival fever","umls","C0031351"
< "13801","pharyngoconjunctival fever","mondo","0005911"
< "13800","inclusion conjunctivitis","icd10cm","A74.0"
< "13800","inclusion conjunctivitis","icd9cm","077.0"
< "13800","inclusion conjunctivitis","mesh","D003235"
< "13800","inclusion conjunctivitis","umls","C0009770"
< "13800","inclusion conjunctivitis","mondo","0005808"
< "0110415","retinitis pigmentosa 2","icd10cm","H35.5"
< "0110415","retinitis pigmentosa 2","mondo","0010723"
< "2127","brain germinoma","umls","C1332606"
< "2127","brain germinoma","mondo","0002214"
< "3883","Lynch syndrome","mesh","D003123"
< "3883","Lynch syndrome","umls","C0009405"
< "3883","Lynch syndrome","umls","C1333990"
< "3883","Lynch syndrome","mondo","0005835"
< "0090030","corticosteroid-binding globulin deficiency","icd10cm","E27.8"
< "0090030","corticosteroid-binding globulin deficiency","mondo","0012675"
< "0014667","disease of metabolism","icd10cm","E88.9"
< "0014667","disease of metabolism","icd9cm","277.9"
< "0014667","disease of metabolism","mesh","D008659"
< "0014667","disease of metabolism","umls","C0025517"
< "0014667","disease of metabolism","mondo","0005066"
---
> "11234","orbital cellulitis","icd10cm","H05.01"
> "11234","orbital cellulitis","icd9cm","376.01"
> "11234","orbital cellulitis","mesh","D054517"
> "11234","orbital cellulitis","umls","C0149507"
> "11234","orbital cellulitis","mondo","0006881"
> "11235","adhesive otitis media","icd10cm","H74.1"
> "11235","adhesive otitis media","icd9cm","385.1"
> "11235","adhesive otitis media","icd9cm","385.10"
> "11235","adhesive otitis media","umls","C0155478"
> "11235","adhesive otitis media","mondo","0001234"
> "4918","renal pelvis adenocarcinoma","umls","C1335748"
> "4918","renal pelvis adenocarcinoma","mondo","0003205"
> "11818","ureteric orifice cancer","icd10cm","C67.6"
> "11818","ureteric orifice cancer","icd9cm","188.6"
> "11818","ureteric orifice cancer","umls","C0153614"
> "11818","ureteric orifice cancer","mondo","0001379"
10260,10267c18144,19957
< "0060755","familial temporal lobe epilepsy 2","mondo","0011965"
< "0060754","familial temporal lobe epilepsy 8","mondo","0014650"
< "0060757","sclerosteosis 2","icd10cm","M85.2"
< "0060757","sclerosteosis 2","mondo","0013679"
< "0060756","sclerosteosis 1","icd10cm","M85.2"
< "0060756","sclerosteosis 1","mondo","0010016"
< "0060751","familial temporal lobe epilepsy 7","mondo","0014639"
< "0060750","familial temporal lobe epilepsy 3","mondo","0012705"
---
> "4916","pituitary carcinoma","mesh","D010911"
> "4916","pituitary carcinoma","umls","C0346300"
> "4916","pituitary carcinoma","mondo","0017582"
> "13574","cortical senile cataract","icd9cm","366.15"
> "13574","cortical senile cataract","umls","C0154980"
> "13574","cortical senile cataract","mondo","0001749"
> "13129","severe pre-eclampsia","icd9cm","642.50"
> "13129","severe pre-eclampsia","umls","C0156669"
> "13129","severe pre-eclampsia","mondo","0001641"
> "13576","twin-to-twin transfusion syndrome","icd10cm","O43.02"
> "13576","twin-to-twin transfusion syndrome","icd10cm","O43.029"
> "13576","twin-to-twin transfusion syndrome","mesh","D005330"
> "13576","twin-to-twin transfusion syndrome","umls","C2909036"
> "13576","twin-to-twin transfusion syndrome","mondo","0019805"
> "4910","urethra adenocarcinoma","umls","C1336885"
> "4910","urethra adenocarcinoma","mondo","0003200"
> "11712","lipoatrophic diabetes mellitus","mesh","D003923"
> "11712","lipoatrophic diabetes mellitus","umls","C0011859"
> "11712","lipoatrophic diabetes mellitus","mondo","0005827"
> "322","myelitis","mesh","D009187"
> "322","myelitis","umls","C0026975"
> "322","myelitis","mondo","0002565"
> "320","vascular myelopathy","icd10cm","G95.1"
> "320","vascular myelopathy","icd9cm","336.1"
> "320","vascular myelopathy","umls","C0154685"
> "320","vascular myelopathy","mondo","0002552"
> "321","tropical spastic paraparesis","icd10cm","G04.1"
> "321","tropical spastic paraparesis","mesh","D015493"
> "321","tropical spastic paraparesis","umls","C0030481"
> "321","tropical spastic paraparesis","mondo","0008039"
> "326","ischemia","mesh","D007511"
> "326","ischemia","umls","C0022116"
> "326","ischemia","mondo","0005053"
> "327","syringomyelia","mesh","D013595"
> "327","syringomyelia","umls","C0039144"
> "327","syringomyelia","mondo","0017987"
> "9892","median arcuate ligament syndrome","icd10cm","I77.4"
> "9892","median arcuate ligament syndrome","icd9cm","447.4"
> "9892","median arcuate ligament syndrome","mesh","D000074742"
> "9892","median arcuate ligament syndrome","umls","C1861783"
> "9892","median arcuate ligament syndrome","mondo","0004914"
> "9893","periodontosis","icd10cm","K05.4"
> "9893","periodontosis","icd9cm","523.5"
> "9893","periodontosis","mesh","D010520"
> "9893","periodontosis","umls","C0600298"
> "9893","periodontosis","mondo","0005076"
> "9898","villonodular synovitis","icd10cm","M12.20"
> "9898","villonodular synovitis","icd9cm","719.2"
> "9898","villonodular synovitis","icd9cm","719.20"
> "9898","villonodular synovitis","umls","C0158168"
> "9898","villonodular synovitis","mondo","0006906"
> "1595","endogenous depression","mesh","D003866"
> "1595","endogenous depression","umls","C0011573"
> "1595","endogenous depression","umls","C0041696"
> "1595","endogenous depression","mondo","0012048"
> "6139","uterine corpus epithelioid leiomyosarcoma","umls","C1519851"
> "6139","uterine corpus epithelioid leiomyosarcoma","mondo","0003782"
> "6132","bronchitis","icd10cm","J20"
> "6132","bronchitis","icd10cm","J20.9"
> "6132","bronchitis","icd10cm","J40"
> "6132","bronchitis","icd10cm","J42"
> "6132","bronchitis","icd9cm","466.0"
> "6132","bronchitis","icd9cm","490"
> "6132","bronchitis","icd9cm","491"
> "6132","bronchitis","icd9cm","491.9"
> "6132","bronchitis","mesh","D001991"
> "6132","bronchitis","mesh","D029481"
> "6132","bronchitis","umls","C0006277"
> "6132","bronchitis","umls","C0008677"
> "6132","bronchitis","umls","C0149514"
> "6132","bronchitis","mondo","0003781"
> "3073","brain glioblastoma multiforme","umls","C0349543"
> "3073","brain glioblastoma multiforme","mondo","0002501"
> "10941","intracranial aneurysm","mesh","D002532"
> "10941","intracranial aneurysm","umls","C0007766"
> "10941","intracranial aneurysm","mondo","0005291"
> "1591","renovascular hypertension","icd10cm","I15.0"
> "1591","renovascular hypertension","mesh","D006978"
> "1591","renovascular hypertension","umls","C0020545"
> "1591","renovascular hypertension","mondo","0006947"
> "10944","tongue disease","icd10cm","K14"
> "10944","tongue disease","icd10cm","K14.9"
> "10944","tongue disease","icd9cm","529.9"
> "10944","tongue disease","mesh","D014060"
> "10944","tongue disease","umls","C0040409"
> "10944","tongue disease","mondo","0001165"
> "9478","postpartum depression","icd10cm","F53"
> "9478","postpartum depression","mesh","D019052"
> "9478","postpartum depression","umls","C0221074"
> "9478","postpartum depression","mondo","0005929"
> "9473","mononeuritis of lower limb","icd9cm","355"
> "9473","mononeuritis of lower limb","icd9cm","355.8"
> "9473","mononeuritis of lower limb","umls","C0154747"
> "9473","mononeuritis of lower limb","mondo","0004797"
> "9470","bacterial meningitis","icd10cm","G00"
> "9470","bacterial meningitis","icd10cm","G00.9"
> "9470","bacterial meningitis","icd9cm","320"
> "9470","bacterial meningitis","icd9cm","320.9"
> "9470","bacterial meningitis","mesh","D016920"
> "9470","bacterial meningitis","umls","C0085437"
> "9470","bacterial meningitis","mondo","0006670"
> "9471","meningitis","icd10cm","G03"
> "9471","meningitis","icd10cm","G03.9"
> "9471","meningitis","icd9cm","322"
> "9471","meningitis","icd9cm","322.9"
> "9471","meningitis","mesh","D008581"
> "9471","meningitis","umls","C0025289"
> "9471","meningitis","mondo","0004796"
> "9476","Sheehan syndrome","icd10cm","E23.0"
> "9476","Sheehan syndrome","mesh","D007018"
> "9476","Sheehan syndrome","umls","C0242342"
> "9476","Sheehan syndrome","mondo","0019618"
> "9477","pulmonary embolism","icd10cm","I26"
> "9477","pulmonary embolism","icd10cm","I26.99"
> "9477","pulmonary embolism","mesh","D011655"
> "9477","pulmonary embolism","umls","C0034065"
> "9477","pulmonary embolism","mondo","0005279"
> "2658","dermoid cyst","icd10cm","K09.8"
> "2658","dermoid cyst","mesh","D003884"
> "2658","dermoid cyst","umls","C0011649"
> "2658","dermoid cyst","mondo","0002378"
> "0050769","N syndrome","mondo","0010686"
> "0050768","mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","icd10cm","E88.8"
> "0050768","mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","mondo","0011421"
> "0050766","choreaacanthocytosis","mesh","D054546"
> "0050766","choreaacanthocytosis","umls","C0393576"
> "0050766","choreaacanthocytosis","mondo","0008695"
> "0050765","neuroacanthocytosis","mesh","D054546"
> "0050765","neuroacanthocytosis","mondo","0016987"
> "0050764","Armfield syndrome","icd10cm","Q87.8"
> "0050764","Armfield syndrome","mondo","0010284"
> "0050763","ARC syndrome","mondo","0017123"
> "0050762","adenylosuccinase lyase deficiency","mondo","0007068"
> "0050760","X-linked myopathy with excessive autophagy","mondo","0010684"
> "0111079","birdshot chorioretinopathy","mesh","C537630"
> "0111079","birdshot chorioretinopathy","umls","C1853959"
> "0111079","birdshot chorioretinopathy","mondo","0011599"
> "0111078","tibial muscular dystrophy","mesh","D049310"
> "0111078","tibial muscular dystrophy","umls","C1838244"
> "0111078","tibial muscular dystrophy","mondo","0010870"
> "0111077","pyruvate kinase deficiency of red cells","mondo","0009950"
> "0111076","progressive familial heart block type IB","mondo","0011474"
> "0111075","progressive familial heart block type II","mondo","0007701"
> "0111074","progressive familial heart block type IA","mondo","0007240"
> "0111073","progressive familial heart block","mondo","0019490"
> "0111072","myostatin-related muscle hypertrophy","mesh","C536106"
> "0111072","myostatin-related muscle hypertrophy","umls","C2931112"
> "0111072","myostatin-related muscle hypertrophy","mondo","0013598"
> "0111071","congenital bile acid synthesis defect 1","mesh","C535442"
> "0111071","congenital bile acid synthesis defect 1","umls","C1843116"
> "0111071","congenital bile acid synthesis defect 1","mondo","0011906"
> "0111070","congenital bile acid synthesis defect 3","mesh","C566340"
> "0111070","congenital bile acid synthesis defect 3","umls","C3151147"
> "0111070","congenital bile acid synthesis defect 3","mondo","0013439"
> "7168","lung occult adenocarcinoma","umls","C1335096"
> "7168","lung occult adenocarcinoma","mondo","0004127"
> "3401","inappropriate ADH syndrome","icd10cm","E22.2"
> "3401","inappropriate ADH syndrome","mesh","D007177"
> "3401","inappropriate ADH syndrome","umls","C0021141"
> "3401","inappropriate ADH syndrome","mondo","0006802"
> "0080316","megalencephalic leukoencephalopathy with subcortical cysts 1","umls","C1858854"
> "0080316","megalencephalic leukoencephalopathy with subcortical cysts 1","mondo","0024555"
> "0080315","megalencephalic leukoencephalopathy with subcortical cysts","mesh","C536141"
> "0080315","megalencephalic leukoencephalopathy with subcortical cysts","mondo","0011391"
> "0060213","FTDALS1","mondo","0007105"
> "0080313","cleft palate-lateral synechia syndrome","icd10cm","Q87.8"
> "0080313","cleft palate-lateral synechia syndrome","mesh","C563047"
> "0080313","cleft palate-lateral synechia syndrome","umls","C0795898"
> "0080313","cleft palate-lateral synechia syndrome","mondo","0007337"
> "0080312","neurodevelopmental disorder with midbrain and hindbrain malformations","mondo","0056797"
> "3407","carotid artery disease","mesh","D002340"
> "3407","carotid artery disease","umls","C0007273"
> "3407","carotid artery disease","mondo","0005269"
> "0080319","X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia","mondo","0010455"
> "0080318","megalencephalic leukoencephalopathy with subcortical cysts 2A","mondo","0013490"
> "4875","trachea adenoid cystic carcinoma","umls","C0345945"
> "4875","trachea adenoid cystic carcinoma","mondo","0006471"
> "13399","color blindness","icd10cm","H53.5"
> "13399","color blindness","icd10cm","H53.50"
> "13399","color blindness","icd9cm","368.5"
> "13399","color blindness","mesh","D003117"
> "13399","color blindness","umls","C0242225"
> "13399","color blindness","mondo","0001703"
> "4877","breast adenoid cystic carcinoma","umls","C1332167"
> "4877","breast adenoid cystic carcinoma","mondo","0003185"
> "4876","trachea carcinoma","umls","C0848879"
> "4876","trachea carcinoma","mondo","0003184"
> "4871","cutaneous adenocystic carcinoma","umls","C0346017"
> "4871","cutaneous adenocystic carcinoma","mondo","0003180"
> "4870","lacrimal gland adenoid cystic carcinoma","umls","C0346340"
> "4870","lacrimal gland adenoid cystic carcinoma","mondo","0006262"
> "4873","anterior horn cell disease","icd9cm","335"
> "4873","anterior horn cell disease","icd9cm","335.9"
> "4873","anterior horn cell disease","mesh","D016472"
> "4873","anterior horn cell disease","umls","C0154681"
> "4873","anterior horn cell disease","mondo","0003182"
> "4872","lung adenoid cystic carcinoma","umls","C1334439"
> "4872","lung adenoid cystic carcinoma","mondo","0003181"
> "4879","Bartholin's gland adenoid cystic carcinoma","umls","C1511047"
> "4879","Bartholin's gland adenoid cystic carcinoma","mondo","0003187"
> "4878","esophageal adenoid cystic carcinoma","umls","C1333441"
> "4878","esophageal adenoid cystic carcinoma","mondo","0003186"
> "0060668","anencephaly","icd10cm","00.0"
> "0060668","anencephaly","mesh","D000757"
> "0060668","anencephaly","mondo","0000819"
> "2068","Bartholin's gland benign neoplasm","umls","C0220616"
> "2068","Bartholin's gland benign neoplasm","mondo","0002193"
> "10610","pancreatic steatorrhea","icd10cm","K90.3"
> "10610","pancreatic steatorrhea","icd9cm","579.4"
> "10610","pancreatic steatorrhea","umls","C0152166"
> "10610","pancreatic steatorrhea","mondo","0001079"
> "13498","urethral syndrome","icd10cm","N34.3"
> "13498","urethral syndrome","icd9cm","597.81"
> "13498","urethral syndrome","umls","C0156279"
> "13498","urethral syndrome","mondo","0001730"
> "2799","bronchiolitis obliterans","mesh","D001989"
> "2799","bronchiolitis obliterans","umls","C0006272"
> "2799","bronchiolitis obliterans","mondo","0015265"
> "10615","acute gonococcal cervicitis","icd9cm","098.15"
> "10615","acute gonococcal cervicitis","umls","C0153195"
> "10615","acute gonococcal cervicitis","mondo","0001080"
> "10616","acute cervicitis","umls","C0269061"
> "10616","acute cervicitis","mondo","0001081"
> "10619","lymph node cancer","umls","C0596869"
> "10619","lymph node cancer","mondo","0001082"
> "2790","necatoriasis","icd10cm","B76.1"
> "2790","necatoriasis","mesh","D009332"
> "2790","necatoriasis","umls","C0027528"
> "2790","necatoriasis","mondo","0005870"
> "7532","squamous papillomatosis","umls","C1378340"
> "7532","squamous papillomatosis","mondo","0004267"
> "2064","vulvar syringoma","umls","C1520099"
> "2064","vulvar syringoma","mondo","0002190"
> "2797","idiopathic interstitial pneumonia","icd10cm","J84.11"
> "2797","idiopathic interstitial pneumonia","icd10cm","J84.112"
> "2797","idiopathic interstitial pneumonia","icd10cm","J84.114"
> "2797","idiopathic interstitial pneumonia","mesh","D011658"
> "2797","idiopathic interstitial pneumonia","umls","C0085786"
> "2797","idiopathic interstitial pneumonia","mondo","0002429"
> "2066","vulvar angiokeratoma","umls","C1274281"
> "2066","vulvar angiokeratoma","mondo","0002192"
> "0110038","Alzheimer's disease 6","icd10cm","G30"
> "0110038","Alzheimer's disease 6","mondo","0011561"
> "0110039","Alzheimer's disease 7","icd10cm","G30"
> "0110039","Alzheimer's disease 7","mondo","0011647"
> "14110","anus cancer","icd10cm","C21.0"
> "14110","anus cancer","icd10cm","C21.1"
> "14110","anus cancer","icd9cm","154.2"
> "14110","anus cancer","icd9cm","154.3"
> "14110","anus cancer","umls","C0153445"
> "14110","anus cancer","umls","C0153446"
> "14110","anus cancer","mondo","0001879"
> "14111","median rhomboid glossitis","icd10cm","K14.2"
> "14111","median rhomboid glossitis","icd9cm","529.2"
> "14111","median rhomboid glossitis","umls","C0155963"
> "14111","median rhomboid glossitis","mondo","0001880"
> "14116","multiple symmetric lipomatosis","mesh","D008069"
> "14116","multiple symmetric lipomatosis","umls","C0024445"
> "14116","multiple symmetric lipomatosis","mondo","0007908"
> "14115","toxic shock syndrome","icd10cm","A48.3"
> "14115","toxic shock syndrome","icd9cm","040.82"
> "14115","toxic shock syndrome","mesh","D012772"
> "14115","toxic shock syndrome","umls","C0600327"
> "14115","toxic shock syndrome","mondo","0001881"
> "0110030","alpha thalassemia-X-linked intellectual disability syndrome","icd10cm","D56.0"
> "0110030","alpha thalassemia-X-linked intellectual disability syndrome","mondo","0010519"
> "0110031","hemoglobin H disease","icd10cm","D56.0"
> "0110031","hemoglobin H disease","mondo","0013512"
> "0110032","autosomal dominant Alport syndrome","mondo","0007086"
> "0110033","autosomal recessive Alport syndrome","mondo","0008762"
> "0110034","X-linked Alport syndrome","mondo","0010520"
> "0110035","Alzheimer's disease 2","icd10cm","G30"
> "0110035","Alzheimer's disease 2","mondo","0007089"
> "0110036","Alzheimer's disease 16","mondo","0010422"
> "0110037","Alzheimer's disease 5","icd10cm","G30"
> "0110037","Alzheimer's disease 5","mondo","0011194"
> "0040032","carbapenem allergy","umls","C0571443"
> "0040033","piperacillin allergy","umls","C0571427"
> "0040030","cefixime allergy","umls","C0571460"
> "0040031","diclofenac allergy","umls","C0570540"
> "0040036","tubocurarine allergy","umls","C0571147"
> "0040037","aztreonam allergy","umls","C0571476"
> "0040034","rocuronium allergy","umls","C0571149"
> "0040035","sulfasalazine allergy","umls","C0570587"
> "13140","suppurative uveitis","mesh","D015829"
> "13140","suppurative uveitis","umls","C0042168"
> "13140","suppurative uveitis","mondo","0006990"
> "13141","uveitis","icd10cm","H20.9"
> "13141","uveitis","mesh","D014605"
> "13141","uveitis","umls","C0042164"
> "13141","uveitis","mondo","0020283"
> "0110598","primary ciliary dyskinesia 14","icd10cm","Q34.8"
> "0110598","primary ciliary dyskinesia 14","mondo","0013434"
> "13145","benign renovascular hypertension","icd9cm","405.11"
> "13145","benign renovascular hypertension","umls","C0155621"
> "13145","benign renovascular hypertension","mondo","0001647"
> "13146","esophageal candidiasis","icd10cm","B37.81"
> "13146","esophageal candidiasis","icd9cm","112.84"
> "13146","esophageal candidiasis","umls","C0239295"
> "13146","esophageal candidiasis","mondo","0001648"
> "13147","fungal esophagitis","umls","C0341109"
> "13147","fungal esophagitis","mondo","0001649"
> "13148","acute cystitis","icd10cm","N30.0"
> "13148","acute cystitis","icd9cm","595.0"
> "13148","acute cystitis","umls","C0149523"
> "13148","acute cystitis","mondo","0001650"
> "9784","trichinosis","icd10cm","B75"
> "9784","trichinosis","icd9cm","124"
> "9784","trichinosis","mesh","D014235"
> "9784","trichinosis","umls","C0040896"
> "9784","trichinosis","mondo","0005992"
> "9786","bulbar polio","icd9cm","045.0"
> "9786","bulbar polio","mesh","D011052"
> "9786","bulbar polio","umls","C0032372"
> "9786","bulbar polio","mondo","0005684"
> "9788","myositis fibrosa","icd10cm","M60.1"
> "9788","myositis fibrosa","icd9cm","728.81"
> "9788","myositis fibrosa","umls","C0158362"
> "9788","myositis fibrosa","mondo","0004881"
> "12554","hemolytic-uremic syndrome","icd10cm","D59.3"
> "12554","hemolytic-uremic syndrome","icd9cm","283.11"
> "12554","hemolytic-uremic syndrome","mesh","D006463"
> "12554","hemolytic-uremic syndrome","umls","C0019061"
> "12554","hemolytic-uremic syndrome","mondo","0001549"
> "13910","red color blindness","icd10cm","H53.54"
> "13910","red color blindness","icd9cm","368.51"
> "13910","red color blindness","mesh","D003117"
> "13910","red color blindness","umls","C0155015"
> "13910","red color blindness","mondo","0010565"
> "0050489","multinodular goiter","mondo","0000334"
> "12969","central nervous system leukemia","umls","C1332884"
> "12969","central nervous system leukemia","mondo","0001606"
> "12961","Poland syndrome","icd10cm","Q79.8"
> "12961","Poland syndrome","mesh","D011045"
> "12961","Poland syndrome","umls","C0032357"
> "12961","Poland syndrome","mondo","0008262"
> "12960","acrocephalosyndactylia","icd9cm","755.55"
> "12960","acrocephalosyndactylia","mesh","D000168"
> "12960","acrocephalosyndactylia","umls","C1510455"
> "12960","acrocephalosyndactylia","mondo","0019796"
> "7097","macrocystic pattern testicular yolk sac tumor","umls","C1515307"
> "7097","macrocystic pattern testicular yolk sac tumor","mondo","0004106"
> "7095","pediatric epithelioid sarcoma","umls","C0279989"
> "7095","pediatric epithelioid sarcoma","mondo","0004105"
> "0060368","Parkinson's disease 2","mondo","0010820"
> "0060369","Parkinson's disease 6","mondo","0011613"
> "0060364","Galloway-Mowat syndrome","mesh","C537548"
> "0060364","Galloway-Mowat syndrome","umls","C0795949"
> "0060364","Galloway-Mowat syndrome","mondo","0009627"
> "0060365","mandibulofacial dysostosis with alopecia","mondo","0014608"
> "0060366","Hennekam syndrome","mesh","C537255"
> "0060366","Hennekam syndrome","umls","C0340834"
> "0060366","Hennekam syndrome","mondo","0016256"
> "0060367","Parkinson's disease 1","mondo","0008200"
> "0060360","hereditary papulotranslucent acrokeratoderma","mesh","C566323"
> "0060360","hereditary papulotranslucent acrokeratoderma","mondo","0007046"
> "0060361","punctate palmoplantar keratoderma","umls","C1274216"
> "0060361","punctate palmoplantar keratoderma","mondo","0017675"
> "0060362","punctate palmoplantar keratoderma type III","mesh","C535653"
> "0060362","punctate palmoplantar keratoderma type III","umls","C0545044"
> "0060362","punctate palmoplantar keratoderma type III","mondo","0007047"
> "0060363","glycerol kinase deficiency","umls","C0574108"
> "0060363","glycerol kinase deficiency","mondo","0010613"
> "8105","extrahepatic bile duct cystadenoma","umls","C1333504"
> "8105","extrahepatic bile duct cystadenoma","mondo","0004462"
> "8104","vaginal tubulovillous adenoma","umls","C1519933"
> "8104","vaginal tubulovillous adenoma","mondo","0004461"
> "8106","cellular phase chronic idiopathic myelofibrosis","umls","C1516553"
> "8106","cellular phase chronic idiopathic myelofibrosis","mondo","0004463"
> "469","deep angioma","umls","C1333265"
> "469","deep angioma","mondo","0003096"
> "468","intramuscular hemangioma","mesh","D006391"
> "468","intramuscular hemangioma","umls","C0205789"
> "468","intramuscular hemangioma","mondo","0003088"
> "8102","fetal adenoma","umls","C0334328"
> "8102","fetal adenoma","mondo","0004460"
> "1352","paranasal sinus disease","mesh","D010254"
> "1352","paranasal sinus disease","umls","C0030469"
> "1352","paranasal sinus disease","mondo","0001735"
> "467","venous hemangioma","umls","C0334532"
> "467","venous hemangioma","mondo","0003083"
> "1350","paranasal sinus neoplasm","mesh","D010255"
> "1350","paranasal sinus neoplasm","umls","C0030470"
> "1350","paranasal sinus neoplasm","mondo","0005289"
> "8109","nephrogenic adenoma of the urethra","umls","C1336889"
> "8109","nephrogenic adenoma of the urethra","mondo","0004464"
> "8108","fibroepithelial polyp of urethra","umls","C1336884"
> "8108","fibroepithelial polyp of urethra","mondo","0006550"
> "1355","paranasal sinus lymphoma","umls","C1335339"
> "1355","paranasal sinus lymphoma","mondo","0001743"
> "6958","aleukemic monocytic leukemia cutis","umls","C1332232"
> "6958","aleukemic monocytic leukemia cutis","mondo","0004051"
> "6959","rectal cloacogenic carcinoma","umls","C1333074"
> "6959","rectal cloacogenic carcinoma","mondo","0004052"
> "6489","periosteal osteogenic sarcoma","umls","C1377843"
> "6489","periosteal osteogenic sarcoma","mondo","0003895"
> "6482","lung acinar adenocarcinoma","umls","C1332137"
> "6482","lung acinar adenocarcinoma","mondo","0003892"
> "6951","telangiectatic osteogenic sarcoma","umls","C0259782"
> "6951","telangiectatic osteogenic sarcoma","mondo","0004050"
> "6481","bladder signet ring cell adenocarcinoma","umls","C1332563"
> "6481","bladder signet ring cell adenocarcinoma","mondo","0003891"
> "6484","mediastinal melanocytic neurilemmoma","umls","C1334668"
> "6484","mediastinal melanocytic neurilemmoma","mondo","0003894"
> "8361","glassy cell variant cervical adenosquamous carcinoma","umls","C1516407"
> "8361","glassy cell variant cervical adenosquamous carcinoma","mondo","0004542"
> "8362","enteric pattern testicular yolk sac tumor","umls","C1515304"
> "8362","enteric pattern testicular yolk sac tumor","mondo","0004543"
> "8369","adult malignant schwannoma","umls","C0278622"
> "8369","adult malignant schwannoma","mondo","0004545"
> "8368","chordoid meningioma","umls","C1370510"
> "8368","chordoid meningioma","mondo","0004544"
> "3184","spinal cord oligodendroglioma","umls","C0346295"
> "3184","spinal cord oligodendroglioma","mondo","0002541"
> "3185","spinal cord glioma","umls","C2937245"
> "3185","spinal cord glioma","mondo","0002542"
> "3186","adult oligodendroglioma","mesh","D009837"
> "3186","adult oligodendroglioma","umls","C0279070"
> "3186","adult oligodendroglioma","umls","C1332190"
> "3186","adult oligodendroglioma","mondo","0002543"
> "3187","brain oligodendroglioma","umls","C0346286"
> "3187","brain oligodendroglioma","mondo","0002544"
> "3181","oligodendroglioma","mesh","D009837"
> "3181","oligodendroglioma","umls","C0028945"
> "3181","oligodendroglioma","umls","C1335110"
> "3181","oligodendroglioma","mondo","0016695"
> "3183","childhood oligodendroglioma","mesh","D009837"
> "3183","childhood oligodendroglioma","umls","C0280475"
> "3183","childhood oligodendroglioma","mondo","0002540"
> "11396","pulmonary edema","icd10cm","J81"
> "11396","pulmonary edema","icd10cm","J81.1"
> "11396","pulmonary edema","mesh","D011654"
> "11396","pulmonary edema","umls","C0034063"
> "11396","pulmonary edema","mondo","0006932"
> "11394","adult respiratory distress syndrome","icd10cm","J80"
> "11394","adult respiratory distress syndrome","mesh","D012128"
> "11394","adult respiratory distress syndrome","umls","C0035222"
> "11394","adult respiratory distress syndrome","mondo","0006502"
> "11390","cerebral arteritis","icd9cm","437.4"
> "11390","cerebral arteritis","umls","C0007773"
> "11390","cerebral arteritis","mondo","0001277"
> "4013","urethra transitional cell carcinoma","umls","C0863015"
> "4013","urethra transitional cell carcinoma","mondo","0002836"
> "4012","papillary transitional carcinoma","umls","C0334274"
> "4012","papillary transitional carcinoma","mondo","0002835"
> "4015","spindle cell carcinoma","mesh","D002277"
> "4015","spindle cell carcinoma","umls","C0205697"
> "4015","spindle cell carcinoma","mondo","0006406"
> "4014","sarcomatoid transitional cell carcinoma","umls","C0334271"
> "4014","sarcomatoid transitional cell carcinoma","mondo","0002837"
> "3985","ostertagiasis","mesh","D010029"
> "3985","ostertagiasis","umls","C0029471"
> "3985","ostertagiasis","mondo","0005891"
> "3981","pantothenate kinase-associated neurodegeneration","icd10cm","G23.0"
> "3981","pantothenate kinase-associated neurodegeneration","mesh","D006211"
> "3981","pantothenate kinase-associated neurodegeneration","umls","C0018523"
> "3981","pantothenate kinase-associated neurodegeneration","mondo","0009319"
> "3982","Meige syndrome","mesh","D008538"
> "3982","Meige syndrome","umls","C0025183"
> "3982","Meige syndrome","mondo","0007920"
> "3983","oesophagostomiasis","mesh","D009814"
> "3983","oesophagostomiasis","umls","C0028887"
> "3983","oesophagostomiasis","mondo","0005880"
> "0080078","hypophosphatemic nephrolithiasis/osteoporosis 2","mondo","0012851"
> "0080079","nonsyndromic congenital nail disorder 1","mondo","0008060"
> "0080072","neuronal intestinal dysplasia","mondo","0000858"
> "0080073","spina bifida occulta","mesh","D016136"
> "0080073","spina bifida occulta","mondo","0000859"
> "0080070","inclusion-cell disease","mondo","0009650"
> "0080071","pseudo-Hurler polydystrophy","mondo","0009651"
> "0080076","Neu-Laxova syndrome 1","mondo","0009736"
> "0080077","hypophosphatemic nephrolithiasis/osteoporosis 1","mondo","0012850"
> "0080074","neural tube defect","mondo","0018075"
> "0080075","Neu-Laxova syndrome 2","mondo","0014466"
> "289","endometriosis","icd10cm","N80"
> "289","endometriosis","icd10cm","N80.9"
> "289","endometriosis","icd9cm","617"
> "289","endometriosis","icd9cm","617.9"
> "289","endometriosis","mesh","D004715"
> "289","endometriosis","umls","C0014175"
> "289","endometriosis","mondo","0005133"
> "288","endometriosis of uterus","icd10cm","N80.0"
> "288","endometriosis of uterus","icd9cm","617.0"
> "288","endometriosis of uterus","mesh","D062788"
> "288","endometriosis of uterus","umls","C0341858"
> "288","endometriosis of uterus","mondo","0010888"
> "1443","cerebral degeneration","icd9cm","331.9"
> "1443","cerebral degeneration","umls","C0154671"
> "1443","cerebral degeneration","mondo","0022687"
> "285","hairy cell leukemia","icd10cm","C91.4"
> "285","hairy cell leukemia","icd10cm","C91.40"
> "285","hairy cell leukemia","icd9cm","202.4"
> "285","hairy cell leukemia","mesh","D007943"
> "285","hairy cell leukemia","umls","C0023443"
> "285","hairy cell leukemia","mondo","0018935"
> "1440","Machado-Joseph disease","mesh","D017827"
> "1440","Machado-Joseph disease","umls","C0024408"
> "1440","Machado-Joseph disease","mondo","0007182"
> "0050997","cerebellar ataxia, mental retardation and dysequlibrium syndrome","mondo","0009133"
> "2477","motor peripheral neuropathy","icd10cm","G60.0"
> "2477","motor peripheral neuropathy","mesh","D015417"
> "2477","motor peripheral neuropathy","umls","C0027888"
> "2477","motor peripheral neuropathy","mondo","0002316"
> "2476","hereditary spastic paraplegia","icd10cm","G11.4"
> "2476","hereditary spastic paraplegia","icd9cm","334.1"
> "2476","hereditary spastic paraplegia","mesh","D015419"
> "2476","hereditary spastic paraplegia","umls","C0037773"
> "2476","hereditary spastic paraplegia","mondo","0019064"
> "2475","chronic conjunctivitis","icd10cm","H10.4"
> "2475","chronic conjunctivitis","icd10cm","H10.40"
> "2475","chronic conjunctivitis","icd9cm","372.1"
> "2475","chronic conjunctivitis","icd9cm","372.10"
> "2475","chronic conjunctivitis","umls","C0155145"
> "2475","chronic conjunctivitis","mondo","0002314"
> "2474","vernal conjunctivitis","icd10cm","H10.44"
> "2474","vernal conjunctivitis","icd9cm","372.13"
> "2474","vernal conjunctivitis","mesh","D003233"
> "2474","vernal conjunctivitis","umls","C0009773"
> "2474","vernal conjunctivitis","mondo","0002313"
> "2473","opportunistic mycosis","icd9cm","118"
> "2473","opportunistic mycosis","umls","C0029119"
> "2473","opportunistic mycosis","mondo","0002312"
> "2479","central nervous system origin vertigo","icd10cm","H81.4"
> "2479","central nervous system origin vertigo","icd10cm","H81.49"
> "2479","central nervous system origin vertigo","icd9cm","386.2"
> "2479","central nervous system origin vertigo","mesh","D014717"
> "2479","central nervous system origin vertigo","umls","C0155503"
> "2479","central nervous system origin vertigo","mondo","0002317"
> "7875","adult xanthogranuloma","umls","C1332220"
> "7875","adult xanthogranuloma","mondo","0004385"
> "7878","uterine corpus atypical polypoid adenomyoma","umls","C1519844"
> "7878","uterine corpus atypical polypoid adenomyoma","mondo","0004386"
> "0110629","Wolfram syndrome 1","icd10cm","E13.8"
> "0110629","Wolfram syndrome 1","mondo","0009101"
> "0110628","primary ciliary dyskinesia 24","icd10cm","Q34.8"
> "0110628","primary ciliary dyskinesia 24","mondo","0014202"
> "0110625","primary ciliary dyskinesia 20","icd10cm","Q34.8"
> "0110625","primary ciliary dyskinesia 20","mondo","0014030"
> "0110624","primary ciliary dyskinesia 30","icd10cm","Q34.8"
> "0110624","primary ciliary dyskinesia 30","mondo","0014465"
> "0110627","primary ciliary dyskinesia 26","icd10cm","Q34.8"
> "0110627","primary ciliary dyskinesia 26","mondo","0014211"
> "0110626","primary ciliary dyskinesia 2","icd10cm","Q34.8"
> "0110626","primary ciliary dyskinesia 2","mondo","0011718"
> "0110621","primary ciliary dyskinesia 17","icd10cm","Q34.8"
> "0110621","primary ciliary dyskinesia 17","mondo","0013854"
> "0110620","primary ciliary dyskinesia 35","mondo","0014910"
> "0110623","primary ciliary dyskinesia 15","icd10cm","Q34.8"
> "0110623","primary ciliary dyskinesia 15","mondo","0013435"
> "0110622","primary ciliary dyskinesia 9","icd10cm","Q34.8"
> "0110622","primary ciliary dyskinesia 9","mondo","0012906"
> "12155","lymphocytic choriomeningitis","icd10cm","A87.2"
> "12155","lymphocytic choriomeningitis","mesh","D008216"
> "12155","lymphocytic choriomeningitis","umls","C0024266"
> "12155","lymphocytic choriomeningitis","mondo","0001449"
> "6307","ectopic thymus","umls","C1333375"
> "6307","ectopic thymus","mondo","0003848"
> "12157","aseptic meningitis","icd10cm","G03.0"
> "12157","aseptic meningitis","mesh","D008582"
> "12157","aseptic meningitis","umls","C0025290"
> "12157","aseptic meningitis","mondo","0006662"
> "10131","psychologic vaginismus","icd10cm","F52.5"
> "10131","psychologic vaginismus","icd9cm","306.51"
> "10131","psychologic vaginismus","umls","C0042266"
> "10131","psychologic vaginismus","mondo","0000946"
> "10132","psychosexual disorder","icd9cm","302.79"
> "10132","psychosexual disorder","umls","C0033951"
> "10132","psychosexual disorder","mondo","0000947"
> "0111539","parastremmatic dwarfism","mesh","C537172"
> "0111539","parastremmatic dwarfism","umls","C1868616"
> "0111536","Buschke-Ollendorff syndrome","mesh","C537415"
> "0111536","Buschke-Ollendorff syndrome","umls","C0265514"
> "0070241","primary coenzyme Q10 deficiency 4","mondo","0012784"
> "0111534","multicentric carpotarsal osteolysis syndrome","mesh","C567171"
> "0111534","multicentric carpotarsal osteolysis syndrome","umls","C2674705"
> "0111535","progressive osseous heteroplasia","mesh","C562735"
> "0111535","progressive osseous heteroplasia","umls","C0334041"
> "10138","xerophthalmia","icd10cm","E50.7"
> "10138","xerophthalmia","icd10cm","H04.12"
> "10138","xerophthalmia","icd9cm","375.15"
> "10138","xerophthalmia","mesh","D014985"
> "10138","xerophthalmia","umls","C0043349"
> "10138","xerophthalmia","mondo","0000948"
> "10139","conjunctival degeneration","icd10cm","H11.10"
> "10139","conjunctival degeneration","icd9cm","372.50"
> "10139","conjunctival degeneration","umls","C0155160"
> "10139","conjunctival degeneration","mondo","0000949"
> "0111530","linear nevus sebaceous syndrome","umls","C3854181"
> "0111531","bilateral optic nerve hypoplasia","umls","C0338502"
> "10428","stable condition keratoconus","icd10cm","H18.61"
> "10428","stable condition keratoconus","icd9cm","371.61"
> "10428","stable condition keratoconus","umls","C0155131"
> "10428","stable condition keratoconus","mondo","0001030"
> "9649","congenital nystagmus","icd10cm","H55.01"
> "9649","congenital nystagmus","icd9cm","379.51"
> "9649","congenital nystagmus","mesh","D020417"
> "9649","congenital nystagmus","umls","C0700501"
> "9649","congenital nystagmus","mondo","0005712"
> "9317","lymphangitis","icd10cm","I89.1"
> "9317","lymphangitis","icd9cm","457.2"
> "9317","lymphangitis","mesh","D008205"
> "9317","lymphangitis","umls","C0024225"
> "9317","lymphangitis","mondo","0005832"
> "10423","acute pericementitis","icd9cm","523.3"
> "10423","acute pericementitis","icd9cm","523.33"
> "10423","acute pericementitis","umls","C0001342"
> "10423","acute pericementitis","mondo","0001028"
> "10426","Klippel-Feil syndrome","icd10cm","Q76.1"
> "10426","Klippel-Feil syndrome","icd9cm","756.16"
> "10426","Klippel-Feil syndrome","mesh","D007714"
> "10426","Klippel-Feil syndrome","umls","C0022738"
> "10426","Klippel-Feil syndrome","mondo","0001029"
> "9640","sarcocystosis","icd10cm","A07.8"
> "9640","sarcocystosis","icd9cm","136.5"
> "9640","sarcocystosis","mesh","D012523"
> "9640","sarcocystosis","umls","C0036231"
> "9640","sarcocystosis","mondo","0018903"
> "9643","babesiosis","icd10cm","B60.0"
> "9643","babesiosis","icd9cm","088.82"
> "9643","babesiosis","mesh","D001404"
> "9643","babesiosis","umls","C0004576"
> "9643","babesiosis","mondo","0005661"
> "9310","nasal cavity neoplasm","umls","C0345630"
> "9310","nasal cavity neoplasm","mondo","0004756"
> "8956","cowpox","icd10cm","B08.010"
> "8956","cowpox","icd9cm","051.01"
> "8956","cowpox","mesh","D015605"
> "8956","cowpox","umls","C0010232"
> "8956","cowpox","mondo","0005720"
> "0110488","autosomal recessive nonsyndromic deafness 3","icd10cm","H90.3"
> "0110488","autosomal recessive nonsyndromic deafness 3","mondo","0010860"
> "0050596","taeniasis","icd10cm","B68.1"
> "0050596","taeniasis","icd9cm","123.2"
> "0050596","taeniasis","umls","C0152073"
> "0050596","taeniasis","mondo","0000367"
> "0050597","intestinal schistosomiasis","icd10cm","B65.1"
> "0050597","intestinal schistosomiasis","icd10cm","B65.2"
> "0050597","intestinal schistosomiasis","icd9cm","120.1"
> "0050597","intestinal schistosomiasis","icd9cm","120.2"
> "0050597","intestinal schistosomiasis","mesh","D012554"
> "0050597","intestinal schistosomiasis","mesh","D012555"
> "0050597","intestinal schistosomiasis","umls","C0036329"
> "0050597","intestinal schistosomiasis","umls","C0036330"
> "0050597","intestinal schistosomiasis","umls","C0276932"
> "0050597","intestinal schistosomiasis","mondo","0008412"
> "0050590","severe congenital neutropenia","icd10cm","D70"
> "0050590","severe congenital neutropenia","mondo","0018542"
> "0050591","tooth agenesis","icd10cm","K00.0"
> "0050591","tooth agenesis","icd9cm","520.0"
> "0050591","tooth agenesis","mesh","D000848"
> "0050591","tooth agenesis","umls","C0399352"
> "0050591","tooth agenesis","mondo","0005486"
> "0050592","asphyxiating thoracic dystrophy","icd10cm","Q77.2"
> "0050592","asphyxiating thoracic dystrophy","mondo","0018770"
> "0050593","primary congenital glaucoma","mondo","0000365"
> "0110481","autosomal recessive nonsyndromic deafness 23","icd10cm","H90.3"
> "0110481","autosomal recessive nonsyndromic deafness 23","mondo","0012293"
> "0110480","autosomal recessive nonsyndromic deafness 22","icd10cm","H90.3"
> "0110480","autosomal recessive nonsyndromic deafness 22","mondo","0011762"
> "0110483","autosomal recessive nonsyndromic deafness 25","icd10cm","H90.3"
> "0110483","autosomal recessive nonsyndromic deafness 25","mondo","0013210"
> "0110482","autosomal recessive nonsyndromic deafness 24","icd10cm","H90.3"
> "0110482","autosomal recessive nonsyndromic deafness 24","mondo","0012602"
> "0110485","autosomal recessive nonsyndromic deafness 27","icd10cm","H90.3"
> "0110485","autosomal recessive nonsyndromic deafness 27","mondo","0011602"
> "0110484","autosomal recessive nonsyndromic deafness 26","icd10cm","H90.3"
> "0110484","autosomal recessive nonsyndromic deafness 26","mondo","0011553"
> "0110487","autosomal recessive nonsyndromic deafness 29","icd10cm","H90.3"
> "0110487","autosomal recessive nonsyndromic deafness 29","mondo","0013537"
> "0110486","autosomal recessive nonsyndromic deafness 28","icd10cm","H90.3"
> "0110486","autosomal recessive nonsyndromic deafness 28","mondo","0012355"
> "0110333","Leber congenital amaurosis 7","icd10cm","H35.5"
> "0110333","Leber congenital amaurosis 7","mondo","0013449"
> "0110332","Leber congenital amaurosis 4","icd10cm","H35.5"
> "0110332","Leber congenital amaurosis 4","mondo","0011458"
> "1631","benign breast phyllodes tumor","icd10cm","D48.6"
> "1631","benign breast phyllodes tumor","mesh","D003557"
> "1631","benign breast phyllodes tumor","umls","C0010701"
> "1631","benign breast phyllodes tumor","umls","C0334501"
> "1631","benign breast phyllodes tumor","umls","C1332533"
> "1631","benign breast phyllodes tumor","mondo","0015871"
> "3216","jejunal somatostatinoma","umls","C1334297"
> "3216","jejunal somatostatinoma","mondo","0002563"
> "1634","breast papillomatosis","umls","C1332636"
> "1634","breast papillomatosis","mondo","0002063"
> "3211","lysosomal storage disease","mesh","D016464"
> "3211","lysosomal storage disease","umls","C0085078"
> "3211","lysosomal storage disease","mondo","0002561"
> "3213","demyelinating disease","mesh","D003711"
> "3213","demyelinating disease","umls","C0011303"
> "3213","demyelinating disease","mondo","0002562"
> "1638","central nervous system tuberculosis","icd9cm","013.2"
> "1638","central nervous system tuberculosis","icd9cm","013.20"
> "1638","central nervous system tuberculosis","mesh","D016862"
> "1638","central nervous system tuberculosis","mesh","D020306"
> "1638","central nervous system tuberculosis","umls","C0085388"
> "1638","central nervous system tuberculosis","mondo","0005696"
> "1639","skeletal tuberculosis","icd10cm","A18.0"
> "1639","skeletal tuberculosis","icd9cm","015"
> "1639","skeletal tuberculosis","icd9cm","015.9"
> "1639","skeletal tuberculosis","mesh","D014394"
> "1639","skeletal tuberculosis","umls","C0041324"
> "1639","skeletal tuberculosis","mondo","0005962"
> "3218","jejunal neoplasm","mesh","D007580"
> "3218","jejunal neoplasm","umls","C0022374"
> "3218","jejunal neoplasm","mondo","0002564"
> "1988","rectum lymphoma","umls","C1335685"
> "1988","rectum lymphoma","mondo","0002166"
> "2815","cranial nerve malignant neoplasm","icd10cm","C72.50"
> "2815","cranial nerve malignant neoplasm","icd9cm","192.0"
> "2815","cranial nerve malignant neoplasm","mesh","D003390"
> "2815","cranial nerve malignant neoplasm","umls","C0153644"
> "2815","cranial nerve malignant neoplasm","mondo","0002433"
> "2814","malignant neoplasm of acoustic nerve","icd10cm","C72.4"
> "2814","malignant neoplasm of acoustic nerve","umls","C0346331"
> "2814","malignant neoplasm of acoustic nerve","mondo","0002432"
> "2817","cranial nerve III tumor","umls","C1263895"
> "2817","cranial nerve III tumor","mondo","0002435"
> "2908","Treacher Collins syndrome","icd10cm","Q75.4"
> "2908","Treacher Collins syndrome","mesh","D008342"
> "2908","Treacher Collins syndrome","umls","C0242387"
> "2908","Treacher Collins syndrome","mondo","0002457"
> "2810","middle lobe syndrome","mesh","D008878"
> "2810","middle lobe syndrome","umls","C0026069"
> "2810","middle lobe syndrome","mondo","0005847"
> "560","jaw-winking syndrome","icd10cm","Q07.8"
> "560","jaw-winking syndrome","icd9cm","374.43"
> "560","jaw-winking syndrome","mesh","C535908"
> "560","jaw-winking syndrome","umls","C0266521"
> "560","jaw-winking syndrome","mondo","0007946"
> "561","trigeminal nerve disease","icd9cm","350.8"
> "561","trigeminal nerve disease","umls","C0029834"
> "561","trigeminal nerve disease","mondo","0003543"
> "562","third cranial nerve disease","umls","C0271353"
> "562","third cranial nerve disease","mondo","0003546"
> "565","bilateral hypoactive labyrinth","icd9cm","386.54"
> "565","bilateral hypoactive labyrinth","umls","C0155518"
> "565","bilateral hypoactive labyrinth","mondo","0003567"
> "566","labyrinthine dysfunction","icd10cm","H83.2"
> "566","labyrinthine dysfunction","icd10cm","H83.2X"
> "566","labyrinthine dysfunction","icd10cm","H83.2X9"
> "566","labyrinthine dysfunction","icd9cm","386.5"
> "566","labyrinthine dysfunction","icd9cm","386.50"
> "566","labyrinthine dysfunction","umls","C0155514"
> "566","labyrinthine dysfunction","mondo","0003571"
> "0050902","medulloblastoma","mesh","D008527"
> "0050902","medulloblastoma","mesh","D018242"
> "0050902","medulloblastoma","umls","C0025149"
> "0050902","medulloblastoma","umls","C0206663"
> "0050902","medulloblastoma","umls","C1334410"
> "0050902","medulloblastoma","mondo","0007959"
> "14705","Pfeiffer syndrome","mesh","D000168"
> "14705","Pfeiffer syndrome","umls","C0220658"
> "14705","Pfeiffer syndrome","mondo","0007043"
> "14256","adult-onset Still's disease","icd10cm","M06.1"
> "14256","adult-onset Still's disease","mesh","D016706"
> "14256","adult-onset Still's disease","umls","C0085253"
> "14256","adult-onset Still's disease","mondo","0019355"
> "14251","vitreoretinal dystrophy","icd10cm","H35.51"
> "14251","vitreoretinal dystrophy","icd9cm","362.73"
> "14251","vitreoretinal dystrophy","umls","C0154863"
> "14251","vitreoretinal dystrophy","mondo","0001923"
> "14250","Down syndrome","icd10cm","Q90"
> "14250","Down syndrome","icd10cm","Q90.9"
> "14250","Down syndrome","icd9cm","758.0"
> "14250","Down syndrome","mesh","D004314"
> "14250","Down syndrome","umls","C0013080"
> "14250","Down syndrome","mondo","0008608"
> "0050905","inflammatory myofibroblastic tumor","mondo","0015798"
> "14252","dystrophies primarily involving the retinal pigment epithelium","icd10cm","H35.54"
> "14252","dystrophies primarily involving the retinal pigment epithelium","icd9cm","362.76"
> "14252","dystrophies primarily involving the retinal pigment epithelium","umls","C0154865"
> "14252","dystrophies primarily involving the retinal pigment epithelium","mondo","0001924"
> "0050909","MALT lymphoma","mondo","0007650"
> "0050908","myelodysplastic syndrome","mesh","D009190"
> "0050908","myelodysplastic syndrome","umls","C2713368"
> "0050908","myelodysplastic syndrome","mondo","0018881"
> "5429","bladder flat intraepithelial lesion","umls","C1332559"
> "5429","bladder flat intraepithelial lesion","mondo","0006111"
> "1188","mononeuropathy","icd10cm","G58.9"
> "1188","mononeuropathy","mesh","D020422"
> "1188","mononeuropathy","umls","C0494491"
> "1188","mononeuropathy","mondo","0001397"
> "5425","ovarian hyperstimulation syndrome","mesh","D016471"
> "5425","ovarian hyperstimulation syndrome","umls","C0085083"
> "5425","ovarian hyperstimulation syndrome","mondo","0011972"
> "3376","bone osteosarcoma","umls","C0585442"
> "3376","bone osteosarcoma","mondo","0002629"
> "5427","urinary bladder villous adenoma","umls","C1336893"
> "5427","urinary bladder villous adenoma","mondo","0003439"
> "5426","premature ovarian failure","icd10cm","E28.3"
> "5426","premature ovarian failure","mesh","D016649"
> "5426","premature ovarian failure","umls","C0085215"
> "5426","premature ovarian failure","mondo","0005387"
> "5421","lung combined type small cell carcinoma","umls","C1333125"
> "5421","lung combined type small cell carcinoma","mondo","0003438"
> "3372","chondroblastic osteosarcoma","umls","C0279603"
> "3372","chondroblastic osteosarcoma","mondo","0002627"
> "3371","chondrosarcoma","mesh","D002813"
> "3371","chondrosarcoma","umls","C0008479"
> "3371","chondrosarcoma","umls","C1335473"
> "3371","chondrosarcoma","mondo","0008977"
> "11887","ureter leiomyoma","umls","C1336875"
> "11887","ureter leiomyoma","mondo","0001399"
> "4248","coronary stenosis","mesh","D023921"
> "4248","coronary stenosis","umls","C0242231"
> "4248","coronary stenosis","mondo","0006715"
> "4249","Gerstmann-Straussler-Scheinker syndrome","icd10cm","A81.82"
> "4249","Gerstmann-Straussler-Scheinker syndrome","icd9cm","046.71"
> "4249","Gerstmann-Straussler-Scheinker syndrome","mesh","D016098"
> "4249","Gerstmann-Straussler-Scheinker syndrome","umls","C0017495"
> "4249","Gerstmann-Straussler-Scheinker syndrome","mondo","0007656"
> "13957","uterine corpus lipoleiomyoma","umls","C1519856"
> "13957","uterine corpus lipoleiomyoma","mondo","0001845"
> "4247","coronary restenosis","mesh","D023903"
> "4247","coronary restenosis","umls","C0948480"
> "4247","coronary restenosis","mondo","0005355"
> "13955","uterus interstitial leiomyoma","icd10cm","D25.1"
> "13955","uterus interstitial leiomyoma","icd9cm","218.1"
> "13955","uterus interstitial leiomyoma","umls","C0153994"
> "13955","uterus interstitial leiomyoma","mondo","0001843"
> "4242","kidney sarcoma","umls","C0346251"
> "4242","kidney sarcoma","mondo","0002930"
> "13951","uterine corpus epithelioid leiomyoma","umls","C1519850"
> "13951","uterine corpus epithelioid leiomyoma","mondo","0001841"
> "5520","head and neck squamous cell carcinoma","mesh","C535575"
> "5520","head and neck squamous cell carcinoma","umls","C1168401"
> "5520","head and neck squamous cell carcinoma","mondo","0010150"
> "5521","keratinizing squamous cell carcinoma","umls","C0334247"
> "5521","keratinizing squamous cell carcinoma","mondo","0005056"
> "5522","basaloid squamous cell carcinoma","umls","C1266005"
> "5522","basaloid squamous cell carcinoma","mondo","0003486"
> "5524","adenoid squamous cell carcinoma","umls","C0334250"
> "5524","adenoid squamous cell carcinoma","umls","C0334393"
> "5524","adenoid squamous cell carcinoma","mondo","0003487"
> "5525","anal squamous cell carcinoma","umls","C1412036"
> "5525","anal squamous cell carcinoma","mondo","0006082"
> "5526","middle ear squamous cell carcinoma","umls","C1334762"
> "5526","middle ear squamous cell carcinoma","mondo","0006303"
> "5527","ampulla of Vater squamous cell carcinoma","umls","C1332251"
> "5527","ampulla of Vater squamous cell carcinoma","mondo","0003490"
> "5528","rectum squamous cell carcinoma","umls","C1335690"
> "5528","rectum squamous cell carcinoma","mondo","0018515"
> "5529","lacrimal gland squamous cell carcinoma","umls","C1334360"
> "5529","lacrimal gland squamous cell carcinoma","mondo","0003492"
> "13653","stenosis of lacrimal punctum","icd10cm","H04.56"
> "13653","stenosis of lacrimal punctum","icd9cm","375.52"
> "13653","stenosis of lacrimal punctum","umls","C0155244"
> "13653","stenosis of lacrimal punctum","mondo","0001767"
> "11889","female breast nipple and areola cancer","icd9cm","174.0"
> "11889","female breast nipple and areola cancer","umls","C0024621"
> "11889","female breast nipple and areola cancer","mondo","0001401"
> "11888","schwannoma of ureter","umls","C1336877"
> "11888","schwannoma of ureter","mondo","0001400"
> "48","male reproductive system disease","icd10cm","N50.9"
> "48","male reproductive system disease","icd9cm","600-608.99"
> "48","male reproductive system disease","icd9cm","608.9"
> "48","male reproductive system disease","mesh","D005832"
> "48","male reproductive system disease","umls","C0017412"
> "48","male reproductive system disease","mondo","0003150"
> "47","prostate disease","icd10cm","N42.9"
> "47","prostate disease","icd9cm","602.9"
> "47","prostate disease","mesh","D011469"
> "47","prostate disease","umls","C0033575"
> "47","prostate disease","mondo","0003105"
> "13654","stenosis of lacrimal passage","icd10cm","H04.54"
> "13654","stenosis of lacrimal passage","icd10cm","H04.549"
> "13654","stenosis of lacrimal passage","icd9cm","375.53"
> "13654","stenosis of lacrimal passage","umls","C0155245"
> "13654","stenosis of lacrimal passage","mondo","0001768"
> "0060649","congenital hereditary endothelial dystrophy of cornea","mondo","0009019"
> "0060648","anterior segment dysgenesis","icd10cm","Q13.8"
> "0060648","anterior segment dysgenesis","mondo","0010015"
> "0060643","primary sclerosing cholangitis","mesh","D015209"
> "0060643","primary sclerosing cholangitis","umls","C0566602"
> "0060643","primary sclerosing cholangitis","mondo","0013433"
> "0060642","recessive dystrophic epidermolysis bullosa","icd10cm","Q81.2"
> "0060642","recessive dystrophic epidermolysis bullosa","mondo","0009179"
> "0060641","endocrine-cerebro-osteodysplasia syndrome","icd10cm","Q87.8"
> "0060641","endocrine-cerebro-osteodysplasia syndrome","mondo","0012980"
> "0060640","ethylmalonic encephalopathy","mesh","C535737"
> "0060640","ethylmalonic encephalopathy","umls","C1865349"
> "0060640","ethylmalonic encephalopathy","mondo","0011229"
> "0060647","cocoon syndrome","mondo","0013334"
> "0060646","congenital chylothorax","mondo","0011331"
> "0060645","chronic recurrent multifocal osteomyelitis","icd10cm","M86.3"
> "0060645","chronic recurrent multifocal osteomyelitis","mesh","C535456"
> "0060645","chronic recurrent multifocal osteomyelitis","mondo","0009813"
> "0060644","chondrodysplasia-pseudohermaphroditism syndrome","mesh","C536123"
> "0060644","chondrodysplasia-pseudohermaphroditism syndrome","umls","C1838654"
> "0060644","chondrodysplasia-pseudohermaphroditism syndrome","mondo","0010814"
> "6547","heart lymphoma","umls","C1332850"
> "6547","heart lymphoma","mondo","0003917"
> "6543","acne","icd10cm","L70"
> "6543","acne","icd10cm","L70.2"
> "6543","acne","icd10cm","L70.9"
> "6543","acne","icd9cm","706.0"
> "6543","acne","mesh","D000152"
> "6543","acne","umls","C0152249"
> "6543","acne","umls","C0702166"
> "6543","acne","mondo","0011438"
> "6548","angiomatous meningioma","mesh","D008579"
> "6548","angiomatous meningioma","umls","C0334608"
> "6548","angiomatous meningioma","mondo","0003918"
> "13656","gastrin secretion abnormality","icd9cm","251.5"
> "13656","gastrin secretion abnormality","umls","C0000774"
> "13656","gastrin secretion abnormality","mondo","0001770"
> "0070075","obsolete Kleefstra Syndrome","mondo","0027407"
> "0070074","autosomal dominant non-syndromic intellectual disability 44","mondo","0014892"
> "345","uterine disease","icd10cm","N85.9"
> "345","uterine disease","icd9cm","621.9"
> "345","uterine disease","mesh","D014591"
> "345","uterine disease","umls","C0042131"
> "345","uterine disease","mondo","0002654"
> "7515","lumbar spinal canal and spinal cord meningioma","umls","C1334436"
> "7515","lumbar spinal canal and spinal cord meningioma","mondo","0004256"
> "7514","Wolffian adnexal neoplasm","mesh","C536741"
> "7514","Wolffian adnexal neoplasm","umls","C1520159"
> "7514","Wolffian adnexal neoplasm","mondo","0004255"
> "341","peripheral vascular disease","icd9cm","443.81"
> "341","peripheral vascular disease","mesh","D016491"
> "341","peripheral vascular disease","umls","C0003838"
> "341","peripheral vascular disease","umls","C0031115"
> "341","peripheral vascular disease","mondo","0005294"
> "342","subclavian artery aneurysm","icd9cm","442.82"
> "342","subclavian artery aneurysm","umls","C0155746"
> "342","subclavian artery aneurysm","mondo","0002641"
> "348","blepharochalasis","icd10cm","H02.3"
> "348","blepharochalasis","icd9cm","374.34"
> "348","blepharochalasis","umls","C0005742"
> "348","blepharochalasis","mondo","0002660"
> "349","systemic mastocytosis","icd10cm","D47.02"
> "349","systemic mastocytosis","mesh","D034721"
> "349","systemic mastocytosis","umls","C0221013"
> "349","systemic mastocytosis","mondo","0016586"
> "7519","endocervical carcinoma","umls","C1299237"
> "7519","endocervical carcinoma","mondo","0004259"
> "7518","inhibited female orgasm","icd10cm","F52.31"
> "7518","inhibited female orgasm","icd9cm","302.73"
> "7518","inhibited female orgasm","umls","C0033948"
> "7518","inhibited female orgasm","mondo","0004258"
> "0060911","karyomegalic interstitial nephritis","icd10cm","N11.8"
> "0060911","karyomegalic interstitial nephritis","mondo","0013898"
> "12105","inflammatory spondylopathy","icd9cm","720.81"
> "12105","inflammatory spondylopathy","umls","C0021396"
> "12105","inflammatory spondylopathy","mondo","0001434"
> "12700","hyperprolactinemia","icd10cm","E22.1"
> "12700","hyperprolactinemia","mesh","D002640"
> "12700","hyperprolactinemia","mesh","D006966"
> "12700","hyperprolactinemia","umls","C0008043"
> "12700","hyperprolactinemia","umls","C0020514"
> "12700","hyperprolactinemia","mondo","0024305"
> "12705","Friedreich ataxia","icd9cm","334.0"
> "12705","Friedreich ataxia","mesh","D005621"
> "12705","Friedreich ataxia","umls","C0016719"
> "12705","Friedreich ataxia","mondo","0009245"
> "12704","ataxia telangiectasia","mesh","D001260"
> "12704","ataxia telangiectasia","umls","C0004135"
> "12704","ataxia telangiectasia","mondo","0008840"
> "12707","myoclonic cerebellar dyssynergia","icd10cm","G11.1"
> "12707","myoclonic cerebellar dyssynergia","mesh","D002527"
> "12707","myoclonic cerebellar dyssynergia","umls","C0007761"
> "12707","myoclonic cerebellar dyssynergia","mondo","0008945"
> "10967","spastic hemiplegia","icd9cm","343.1"
> "10967","spastic hemiplegia","umls","C0270805"
> "10967","spastic hemiplegia","mondo","0001168"
> "6723","malignant type AB thymoma","umls","C1266093"
> "6723","malignant type AB thymoma","mondo","0003976"
> "10965","spastic diplegia","icd10cm","G80.1"
> "10965","spastic diplegia","icd9cm","343.0"
> "10965","spastic diplegia","mesh","D002547"
> "10965","spastic diplegia","umls","C0023882"
> "10965","spastic diplegia","umls","C0154695"
> "10965","spastic diplegia","mondo","0001167"
> "10964","cholesteatoma of middle ear","icd10cm","H71"
> "10964","cholesteatoma of middle ear","icd9cm","385.3"
> "10964","cholesteatoma of middle ear","icd9cm","385.32"
> "10964","cholesteatoma of middle ear","icd9cm","385.33"
> "10964","cholesteatoma of middle ear","mesh","D018424"
> "10964","cholesteatoma of middle ear","umls","C0008374"
> "10964","cholesteatoma of middle ear","umls","C0155490"
> "10964","cholesteatoma of middle ear","mondo","0006533"
> "10963","cholesteatoma of attic","icd10cm","H71.0"
> "10963","cholesteatoma of attic","icd10cm","H71.00"
> "10963","cholesteatoma of attic","icd9cm","385.31"
> "10963","cholesteatoma of attic","umls","C0155489"
> "10963","cholesteatoma of attic","mondo","0006531"
> "6721","Littre gland carcinoma","umls","C1516285"
> "6721","Littre gland carcinoma","mondo","0003975"
> "10969","hemiplegia","icd9cm","343.4"
> "10969","hemiplegia","mesh","D006429"
> "10969","hemiplegia","umls","C0392550"
> "10969","hemiplegia","mondo","0001170"
> "10968","spastic monoplegia","icd9cm","343.3"
> "10968","spastic monoplegia","mesh","D002547"
> "10968","spastic monoplegia","umls","C0154698"
> "10968","spastic monoplegia","mondo","0001169"
> "13454","gonococcal synovitis","icd9cm","098.51"
> "13454","gonococcal synovitis","umls","C0343714"
> "13454","gonococcal synovitis","mondo","0001720"
> "8302","mixed endometrial stromal and smooth muscle tumor","umls","C1513364"
> "8302","mixed endometrial stromal and smooth muscle tumor","mondo","0004526"
> "13453","gonococcal bursitis","icd10cm","A54.49"
> "13453","gonococcal bursitis","icd9cm","098.52"
> "13453","gonococcal bursitis","umls","C0153218"
> "13453","gonococcal bursitis","mondo","0001719"
> "0050749","peripheral T-cell lymphoma","mondo","0000430"
> "4837","Gorham's disease","mesh","D010015"
> "4837","Gorham's disease","umls","C0029436"
> "4837","Gorham's disease","mondo","0003157"
> "0050741","alcohol dependence","kegg","05034"
> "0050741","alcohol dependence","mondo","0007079"
> "0050740","Qazi Markouizos syndrome","mesh","C536259"
> "0050740","Qazi Markouizos syndrome","mondo","0010816"
> "0050290","trichosporonosis","mesh","D060586"
> "0050290","trichosporonosis","mondo","0000306"
> "0050745","diffuse large B-cell lymphoma","mondo","0018905"
> "0050747","lymphoplasmacytic lymphoma","icd10cm","C88.0"
> "0050747","lymphoplasmacytic lymphoma","icd9cm","273.3"
> "0050747","lymphoplasmacytic lymphoma","mesh","D008258"
> "0050747","lymphoplasmacytic lymphoma","umls","C0024419"
> "0050747","lymphoplasmacytic lymphoma","umls","C2936755"
> "0050747","lymphoplasmacytic lymphoma","mondo","0000432"
> "0050746","mantle cell lymphoma","mesh","D020522"
> "0050746","mantle cell lymphoma","mondo","0018876"
> "8208","lung superior sulcus carcinoma","umls","C1336529"
> "8208","lung superior sulcus carcinoma","mondo","0004500"
> "0111059","Bernard-Soulier syndrome type A2","mondo","0007930"
> "0111058","platelet-type bleeding disorder 12","mondo","0011588"
> "0111051","platelet-type bleeding disorder 18","icd10cm","D69.1"
> "0111051","platelet-type bleeding disorder 18","mondo","0014386"
> "0111050","Quebec platelet disorder","mesh","C536260"
> "0111050","Quebec platelet disorder","umls","C1866423"
> "0111050","Quebec platelet disorder","mondo","0011136"
> "0111053","platelet-type bleeding disorder 15","mondo","0014078"
> "0111052","Scott syndrome","mesh","C563120"
> "0111052","Scott syndrome","umls","C0796149"
> "0111052","Scott syndrome","mondo","0009885"
> "0111055","platelet-type bleeding disorder 20","mondo","0014830"
> "0111054","von Willebrand's disease 3","mesh","D056729"
> "0111054","von Willebrand's disease 3","umls","C1264041"
> "0111054","von Willebrand's disease 3","mondo","0010191"
> "0111057","platelet-type bleeding disorder 11","icd10cm","D69.8"
> "0111057","platelet-type bleeding disorder 11","mondo","0013623"
> "0111056","platelet-type bleeding disorder 3","icd10cm","D69.8"
> "0111056","platelet-type bleeding disorder 3","mondo","0008332"
> "0050127","sinusitis","icd10cm","J01"
> "0050127","sinusitis","icd10cm","J01.9"
> "0050127","sinusitis","icd10cm","J01.90"
> "0050127","sinusitis","icd9cm","461"
> "0050127","sinusitis","icd9cm","461.9"
> "0050127","sinusitis","mesh","D012852"
> "0050127","sinusitis","umls","C0149512"
> "0050127","sinusitis","mondo","0005961"
> "0050120","hemophagocytic lymphohistiocytosis","icd10cm","D76.1"
> "0050120","hemophagocytic lymphohistiocytosis","mesh","D051359"
> "0050120","hemophagocytic lymphohistiocytosis","umls","C0024291"
> "0050120","hemophagocytic lymphohistiocytosis","mondo","0015540"
> "9439","chronic cholangitis","umls","C0267918"
> "9439","chronic cholangitis","mondo","0004786"
> "11269","chronic apical periodontitis","icd10cm","K04.5"
> "11269","chronic apical periodontitis","icd9cm","522.6"
> "11269","chronic apical periodontitis","umls","C0392492"
> "11269","chronic apical periodontitis","mondo","0001251"
> "0080331","cold-induced sweating syndrome 3","mondo","0014890"
> "0080330","cold-induced sweating syndrome 2","mondo","0012467"
> "0080333","aortic valve disease 1","mondo","0024523"
> "0080332","bicuspid aortic valve disease","mondo","0007194"
> "0080335","mitochondrial DNA depletion syndrome 12b","mondo","0014175"
> "0080334","aortic valve disease 2","mondo","0013902"
> "0080337","mitochondrial DNA depletion syndrome 15","mondo","0014943"
> "0080336","mitochondrial DNA depletion syndrome 14","mondo","0014820"
> "0080339","familial erythrocytosis 4","mondo","0012729"
> "0080338","familial erythrocytosis 3","mondo","0012353"
> "4813","adult brain stem glioma","umls","C0278873"
> "4813","adult brain stem glioma","mondo","0003153"
> "4812","adult brainstem gliosarcoma","umls","C1377914"
> "4812","adult brainstem gliosarcoma","mondo","0003152"
> "2044","drug-induced hepatitis","mesh","D056487"
> "2044","drug-induced hepatitis","umls","C0524912"
> "2044","drug-induced hepatitis","mondo","0002184"
> "4810","cerebrotendinous xanthomatosis","mesh","D019294"
> "4810","cerebrotendinous xanthomatosis","umls","C0238052"
> "4810","cerebrotendinous xanthomatosis","mondo","0008948"
> "4817","ganglioneuroma","mesh","D005729"
> "4817","ganglioneuroma","umls","C0017075"
> "4817","ganglioneuroma","umls","C1513025"
> "4817","ganglioneuroma","mondo","0005033"
> "2043","hepatitis B","mesh","D006509"
> "2043","hepatitis B","umls","C0019163"
> "2043","hepatitis B","mondo","0005344"
> "2048","autoimmune hepatitis","icd10cm","K75.4"
> "2048","autoimmune hepatitis","icd9cm","571.42"
> "2048","autoimmune hepatitis","mesh","D019693"
> "2048","autoimmune hepatitis","umls","C0241910"
> "2048","autoimmune hepatitis","umls","C1332355"
> "2048","autoimmune hepatitis","mondo","0016264"
> "9410","panhypopituitarism","icd10cm","E23.0"
> "9410","panhypopituitarism","icd9cm","253.2"
> "9410","panhypopituitarism","mesh","C580003"
> "9410","panhypopituitarism","umls","C0242343"
> "9410","panhypopituitarism","mondo","0019591"
> "11615","penile cancer","icd10cm","C60"
> "11615","penile cancer","icd10cm","C60.2"
> "11615","penile cancer","icd10cm","C60.9"
> "11615","penile cancer","icd9cm","187.3"
> "11615","penile cancer","icd9cm","187.4"
> "11615","penile cancer","mesh","D010412"
> "11615","penile cancer","umls","C0153600"
> "11615","penile cancer","umls","C0153601"
> "11615","penile cancer","mondo","0001325"
> "11612","polycystic ovary syndrome","icd10cm","E28.2"
> "11612","polycystic ovary syndrome","icd9cm","256.4"
> "11612","polycystic ovary syndrome","mesh","D011085"
> "11612","polycystic ovary syndrome","umls","C0032460"
> "11612","polycystic ovary syndrome","mondo","0008487"
> "9415","allergic asthma","icd10cm","J45"
> "9415","allergic asthma","icd9cm","493.0"
> "9415","allergic asthma","umls","C0155877"
> "9415","allergic asthma","mondo","0004784"
> "11262","ornithosis","icd10cm","A70"
> "11262","ornithosis","icd9cm","073"
> "11262","ornithosis","icd9cm","073.9"
> "11262","ornithosis","mesh","D009956"
> "11262","ornithosis","umls","C0029291"
> "11262","ornithosis","mondo","0005888"
> "10632","Wolfram syndrome","mesh","D014929"
> "10632","Wolfram syndrome","umls","C0043207"
> "10632","Wolfram syndrome","mondo","0018105"
> "10631","partial optic atrophy","icd9cm","377.15"
> "10631","partial optic atrophy","umls","C0155295"
> "10631","partial optic atrophy","mondo","0001086"
> "14139","anus lymphoma","umls","C1332268"
> "14139","anus lymphoma","mondo","0001888"
> "9341","urethral diverticulum","icd10cm","N36.1"
> "9341","urethral diverticulum","icd9cm","599.2"
> "9341","urethral diverticulum","umls","C0152443"
> "9341","urethral diverticulum","mondo","0004761"
> "14130","lateral cystocele","icd10cm","N81.12"
> "14130","lateral cystocele","icd9cm","618.02"
> "14130","lateral cystocele","umls","C2711750"
> "14130","lateral cystocele","mondo","0001885"
> "14131","midline cystocele","icd10cm","N81.11"
> "14131","midline cystocele","icd9cm","618.01"
> "14131","midline cystocele","umls","C1456248"
> "14131","midline cystocele","mondo","0001886"
> "14133","Masters-Allen syndrome","icd9cm","620.6"
> "14133","Masters-Allen syndrome","umls","C0152079"
> "14133","Masters-Allen syndrome","mondo","0001887"
> "11080","myiasis","icd10cm","B87"
> "11080","myiasis","icd10cm","B87.9"
> "11080","myiasis","icd9cm","134.0"
> "11080","myiasis","mesh","D009198"
> "11080","myiasis","umls","C0027030"
> "11080","myiasis","mondo","0019147"
> "0070277","primary autosomal recessive microcephaly 15","mondo","0014660"
> "0070276","hereditary nonpolyposis colorectal cancer type 7","mondo","0013725"
> "0070275","hereditary nonpolyposis colorectal cancer type 4","mondo","0013699"
> "0070274","hereditary nonpolyposis colorectal cancer type 2","mondo","0012249"
> "0070273","hereditary nonpolyposis colorectal cancer type 6","mondo","0013695"
> "0070272","hereditary nonpolyposis colorectal cancer type 5","mondo","0013710"
> "0070271","Lynch syndrome 1","mondo","0007356"
> "0070270","hereditary nonpolyposis colorectal cancer type 8","mondo","0013196"
> "0070279","primary autosomal recessive microcephaly 14","mondo","0014623"
> "0070278","primary autosomal recessive microcephaly 7","mondo","0012989"
> "0110012","advanced sleep phase syndrome 2","mondo","0014088"
> "0110013","advanced sleep phase syndrome 3","mondo","0014814"
> "0110010","achromatopsia 4","mondo","0013465"
> "0110011","advanced sleep phase syndrome 1","mondo","0011442"
> "0110016","Leber congenital amaurosis 2","icd10cm","H35.5"
> "0110016","Leber congenital amaurosis 2","mondo","0008765"
> "0110017","age related macular degeneration 4","mondo","0012540"
> "0110014","age related macular degeneration 1","mondo","0011285"
> "0110015","age related macular degeneration 2","mondo","0007932"
> "0110018","age related macular degeneration 6","mondo","0013406"
> "0110019","age related macular degeneration 7","mondo","0012419"
> "0110548","autosomal dominant nonsyndromic deafness 17","icd10cm","H90.3"
> "0110548","autosomal dominant nonsyndromic deafness 17","mondo","0011350"
> "0110549","autosomal dominant nonsyndromic deafness 18","icd10cm","H90.3"
> "0110549","autosomal dominant nonsyndromic deafness 18","mondo","0011625"
> "12156","arachnoiditis","icd10cm","G03"
> "12156","arachnoiditis","mesh","D001100"
> "12156","arachnoiditis","umls","C0003708"
> "12156","arachnoiditis","mondo","0015304"
> "0060346","Native American myopathy","mesh","C538343"
> "0060346","Native American myopathy","umls","C1850625"
> "0060346","Native American myopathy","mondo","0009722"
> "0060347","acrorenal syndrome","mesh","C563159"
> "0060347","acrorenal syndrome","umls","C3495490"
> "0060347","acrorenal syndrome","mondo","0007059"
> "0060344","acrodermatitis chronica atrophicans","icd9cm","701.8"
> "0060344","acrodermatitis chronica atrophicans","umls","C0029805"
> "0060344","acrodermatitis chronica atrophicans","mondo","0006524"
> "0060345","bacillary angiomatosis","mesh","D016917"
> "0060345","bacillary angiomatosis","umls","C0085434"
> "0060345","bacillary angiomatosis","mondo","0000758"
> "0060342","acromelic frontonasal dysostosis","mesh","C566345"
> "0060342","acromelic frontonasal dysostosis","mondo","0011359"
> "7079","adult cystic teratoma","umls","C1368888"
> "7079","adult cystic teratoma","mondo","0004099"
> "0060341","agnathia-otocephaly complex","icd10cm","Q18.2"
> "0060341","agnathia-otocephaly complex","mesh","C562503"
> "0060341","agnathia-otocephaly complex","mondo","0008740"
> "7076","lipid-rich breast carcinoma","umls","C1517894"
> "7076","lipid-rich breast carcinoma","mondo","0021090"
> "7077","malignant melanocytic peripheral nerve sheath tumor of mediastinum","umls","C1334600"
> "7077","malignant melanocytic peripheral nerve sheath tumor of mediastinum","mondo","0004098"
> "7071","spinal cord dermoid cyst","umls","C1333278"
> "7071","spinal cord dermoid cyst","mondo","0004096"
> "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","mesh","C537157"
> "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","umls","C1855840"
> "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","mondo","0009426"
> "0060349","microcephaly with or without chorioretinopathy, lymphedema, or mental retardation","mesh","C537711"
> "0060349","microcephaly with or without chorioretinopathy, lymphedema, or mental retardation","umls","C1835265"
> "0060349","microcephaly with or without chorioretinopathy, lymphedema, or mental retardation","mondo","0007918"
> "14397","protozoal dysentery","icd10cm","A07.8"
> "14397","protozoal dysentery","icd9cm","007.8"
> "14397","protozoal dysentery","umls","C0152507"
> "14397","protozoal dysentery","mondo","0001955"
> "14392","thrombophlebitis migrans","icd10cm","I82.1"
> "14392","thrombophlebitis migrans","icd9cm","453.1"
> "14392","thrombophlebitis migrans","umls","C0152250"
> "14392","thrombophlebitis migrans","mondo","0001954"
> "6976","micropapillary variant infiltrating bladder urothelial carcinoma","umls","C1517579"
> "6976","micropapillary variant infiltrating bladder urothelial carcinoma","mondo","0004057"
> "8162","thyroid Hurthle cell adenoma","umls","C1336750"
> "8162","thyroid Hurthle cell adenoma","mondo","0004483"
> "8161","thyroid gland Hurthle cell carcinoma","mesh","C536913"
> "8161","thyroid gland Hurthle cell carcinoma","umls","C0749424"
> "8161","thyroid gland Hurthle cell carcinoma","mondo","0011836"
> "6975","bladder urothelial papillary carcinoma","umls","C1518882"
> "6975","bladder urothelial papillary carcinoma","mondo","0004056"
> "8167","gallbladder melanoma","umls","C1333749"
> "8167","gallbladder melanoma","mondo","0004484"
> "6970","acute inflammation of lacrimal passage","icd10cm","H04.3"
> "6970","acute inflammation of lacrimal passage","icd9cm","375.3"
> "6970","acute inflammation of lacrimal passage","umls","C0339129"
> "6970","acute inflammation of lacrimal passage","mondo","0004055"
> "0060123","connective tissue benign neoplasm","mesh","D012983"
> "0060123","connective tissue benign neoplasm","umls","C0037579"
> "0060123","connective tissue benign neoplasm","mondo","0000654"
> "0060127","gamma heavy chain disease","mondo","0015046"
> "0060125","heavy chain disease","icd10cm","C88.2"
> "0060125","heavy chain disease","mesh","D006362"
> "0060125","heavy chain disease","umls","C0018852"
> "0060125","heavy chain disease","umls","C0018854"
> "0060125","heavy chain disease","umls","C0242310"
> "0060125","heavy chain disease","mondo","0019464"
> "0001816","angiosarcoma","mesh","D006394"
> "0001816","angiosarcoma","umls","C0018923"
> "0001816","angiosarcoma","umls","C0854893"
> "0001816","angiosarcoma","mondo","0016982"
> "8389","lumbar plexus neoplasm","umls","C1334437"
> "8389","lumbar plexus neoplasm","mondo","0004546"
> "4389","soft tissue peripheral neuroepithelioma","umls","C1112437"
> "4389","soft tissue peripheral neuroepithelioma","mondo","0002982"
> "4388","bone peripheral neuroepithelioma","umls","C0855009"
> "4388","bone peripheral neuroepithelioma","mondo","0002981"
> "4386","myofibroma","mesh","D047708"
> "4386","myofibroma","umls","C1266121"
> "4386","myofibroma","mondo","0006312"
> "4385","papillary squamous carcinoma","umls","C0334244"
> "4385","papillary squamous carcinoma","mondo","0002979"
> "4384","orbit alveolar rhabdomyosarcoma","umls","C1335126"
> "4384","orbit alveolar rhabdomyosarcoma","mondo","0002978"
> "407","hepatic tuberculosis","mesh","D014386"
> "407","hepatic tuberculosis","umls","C0041313"
> "407","hepatic tuberculosis","mondo","0005787"
> "1373","endometrial stromal nodule","umls","C0334485"
> "1373","endometrial stromal nodule","mondo","0001783"
> "404","gastrointestinal tuberculosis","mesh","D014385"
> "404","gastrointestinal tuberculosis","umls","C0041312"
> "404","gastrointestinal tuberculosis","mondo","0005768"
> "403","mouth disease","mesh","D009059"
> "403","mouth disease","umls","C0026636"
> "403","mouth disease","mondo","0006858"
> "402","oral tuberculosis","mesh","D014393"
> "402","oral tuberculosis","umls","C0041323"
> "402","oral tuberculosis","mondo","0005887"
> "401","multidrug-resistant tuberculosis","mesh","D018088"
> "401","multidrug-resistant tuberculosis","umls","C0206526"
> "401","multidrug-resistant tuberculosis","mondo","0005861"
> "409","liver disease","icd10cm","K70-K77"
> "409","liver disease","icd10cm","K76.9"
> "409","liver disease","icd9cm","573.9"
> "409","liver disease","mesh","D008107"
> "409","liver disease","umls","C0023895"
> "409","liver disease","mondo","0005154"
> "4031","eosinophilic gastroenteritis","icd9cm","558.41"
> "4031","eosinophilic gastroenteritis","mesh","C535952"
> "4031","eosinophilic gastroenteritis","umls","C1262481"
> "4031","eosinophilic gastroenteritis","mondo","0016129"
> "4030","eosinophilic gastritis","icd9cm","535.7"
> "4030","eosinophilic gastritis","mesh","C535952"
> "4030","eosinophilic gastritis","umls","C0267154"
> "4030","eosinophilic gastritis","mondo","0002840"
> "4033","bacterial gastritis","umls","C0948039"
> "4033","bacterial gastritis","mondo","0002842"
> "4035","lymphocytic gastritis","umls","C1283271"
> "4035","lymphocytic gastritis","mondo","0002844"
> "4034","fungal gastritis","umls","C0948638"
> "4034","fungal gastritis","mondo","0002843"
> "4037","necrotizing gastritis","umls","C0877152"
> "4037","necrotizing gastritis","mondo","0002845"
> "4038","granulomatous gastritis","icd10cm","K29.6"
> "4038","granulomatous gastritis","umls","C1112577"
> "4038","granulomatous gastritis","mondo","0002846"
> "11379","gnathomiasis","icd10cm","B83.1"
> "11379","gnathomiasis","icd9cm","128.1"
> "11379","gnathomiasis","mesh","D058429"
> "11379","gnathomiasis","umls","C0018013"
> "11379","gnathomiasis","mondo","0005776"
> "11374","anal spasm","icd10cm","K59.4"
> "11374","anal spasm","icd9cm","564.6"
> "11374","anal spasm","umls","C0152167"
> "11374","anal spasm","mondo","0001274"
> "11371","functional diarrhea","icd10cm","K59.1"
> "11371","functional diarrhea","icd9cm","564.5"
> "11371","functional diarrhea","umls","C0156173"
> "11371","functional diarrhea","mondo","0001272"
> "11372","megacolon","icd10cm","K59.3"
> "11372","megacolon","icd10cm","K59.39"
> "11372","megacolon","mesh","D008531"
> "11372","megacolon","umls","C0025160"
> "11372","megacolon","mondo","0001273"
> "14435","chronic tubotympanic suppurative otitis media","icd10cm","H66.1"
> "14435","chronic tubotympanic suppurative otitis media","icd10cm","H66.10"
> "14435","chronic tubotympanic suppurative otitis media","icd9cm","382.1"
> "14435","chronic tubotympanic suppurative otitis media","umls","C0155440"
> "14435","chronic tubotympanic suppurative otitis media","mondo","0001964"
> "2458","papillary conjunctivitis","umls","C0854165"
> "2458","papillary conjunctivitis","mondo","0002309"
> "2455","angular blepharoconjunctivitis","icd10cm","H10.52"
> "2455","angular blepharoconjunctivitis","icd9cm","372.21"
> "2455","angular blepharoconjunctivitis","umls","C0155149"
> "2455","angular blepharoconjunctivitis","mondo","0002306"
> "2457","giant papillary conjunctivitis","mesh","D003233"
> "2457","giant papillary conjunctivitis","umls","C0009769"
> "2457","giant papillary conjunctivitis","mondo","0002308"
> "2456","blepharoconjunctivitis","icd10cm","H10.5"
> "2456","blepharoconjunctivitis","icd10cm","H10.50"
> "2456","blepharoconjunctivitis","icd9cm","372.2"
> "2456","blepharoconjunctivitis","icd9cm","372.20"
> "2456","blepharoconjunctivitis","umls","C0005743"
> "2456","blepharoconjunctivitis","mondo","0002307"
> "2451","protein S deficiency","icd10cm","D68.59"
> "2451","protein S deficiency","mesh","D018455"
> "2451","protein S deficiency","umls","C0242666"
> "2451","protein S deficiency","mondo","0002304"
> "2450","central retinal vein occlusion","icd10cm","H34.81"
> "2450","central retinal vein occlusion","icd9cm","362.35"
> "2450","central retinal vein occlusion","umls","C0154841"
> "2450","central retinal vein occlusion","mondo","0002303"
> "2452","thrombophilia","icd10cm","D68.59"
> "2452","thrombophilia","mesh","D019851"
> "2452","thrombophilia","umls","C0398623"
> "2452","thrombophilia","mondo","0002305"
> "7851","pancreatic intraductal papillary-mucinous adenoma","umls","C1518868"
> "7851","pancreatic intraductal papillary-mucinous adenoma","mondo","0004381"
> "0070048","autosomal dominant non-syndromic intellectual disability 18","mondo","0014034"
> "0070049","autosomal dominant non-syndromic intellectual disability 19","mondo","0014035"
> "0070044","Coffin-Siris syndrome 2","mondo","0013819"
> "0070045","Coffin-Siris syndrome 3","mondo","0013820"
> "0070046","Coffin-Siris syndrome 4","mondo","0013821"
> "0070047","Schuurs-Hoeijmakers Syndrome","mondo","0014006"
> "0070040","autosomal dominant non-syndromic intellectual disability 10","mondo","0013657"
> "0070041","autosomal dominant non-syndromic intellectual disability 11","mondo","0013658"
> "0070042","Coffin-Siris syndrome 1","mondo","0013804"
> "0070043","autosomal dominant non-syndromic intellectual disability 13","mondo","0013805"
> "12139","dysthymic disorder","icd10cm","F34.1"
> "12139","dysthymic disorder","icd9cm","300.4"
> "12139","dysthymic disorder","mesh","D019263"
> "12139","dysthymic disorder","umls","C0013415"
> "12139","dysthymic disorder","mondo","0001442"
> "12132","granulomatosis with polyangiitis","icd10cm","M31.3"
> "12132","granulomatosis with polyangiitis","icd10cm","M31.30"
> "12132","granulomatosis with polyangiitis","icd9cm","446.4"
> "12132","granulomatosis with polyangiitis","mesh","D014890"
> "12132","granulomatosis with polyangiitis","umls","C3495801"
> "12132","granulomatosis with polyangiitis","mondo","0012105"
> "6367","acral lentiginous melanoma","mondo","0003865"
> "12134","factor VIII deficiency","icd10cm","D66"
> "12134","factor VIII deficiency","icd9cm","286.0"
> "12134","factor VIII deficiency","mesh","D006467"
> "12134","factor VIII deficiency","umls","C0019069"
> "12134","factor VIII deficiency","mondo","0010602"
> "6364","migraine","icd10cm","G43"
> "6364","migraine","icd10cm","G43.9"
> "6364","migraine","icd10cm","G43.909"
> "6364","migraine","icd9cm","346"
> "6364","migraine","icd9cm","346.9"
> "6364","migraine","mesh","D008881"
> "6364","migraine","umls","C0042331"
> "6364","migraine","umls","C0149931"
> "6364","migraine","mondo","0005277"
> "9335","scotoma","icd10cm","H53.42"
> "9335","scotoma","icd10cm","H53.45"
> "9335","scotoma","icd9cm","368.42"
> "9335","scotoma","icd9cm","368.44"
> "9335","scotoma","mesh","D012607"
> "9335","scotoma","umls","C0029657"
> "9335","scotoma","umls","C0152192"
> "9335","scotoma","mondo","0004758"
> "10153","ileum cancer","icd10cm","C17.2"
> "10153","ileum cancer","icd9cm","152.2"
> "10153","ileum cancer","umls","C0153428"
> "10153","ileum cancer","mondo","0000955"
> "9336","bestiality","icd9cm","302.1"
> "9336","bestiality","umls","C0152186"
> "9336","bestiality","mondo","0004759"
> "10156","ileal neoplasm","mesh","D007078"
> "10156","ileal neoplasm","umls","C0020876"
> "10156","ileal neoplasm","mondo","0006801"
> "10154","small intestine cancer","icd10cm","C17"
> "10154","small intestine cancer","icd10cm","C17.9"
> "10154","small intestine cancer","icd9cm","152.9"
> "10154","small intestine cancer","umls","C0153425"
> "10154","small intestine cancer","mondo","0000956"
> "10155","intestinal cancer","icd10cm","C26.0"
> "10155","intestinal cancer","icd9cm","159.0"
> "10155","intestinal cancer","mesh","D007414"
> "10155","intestinal cancer","umls","C0346627"
> "10155","intestinal cancer","mondo","0005814"
> "0111550","scalp-ear-nipple syndrome","mesh","C536623"
> "0111550","scalp-ear-nipple syndrome","umls","C1867020"
> "0111551","neurogenic scapuloperoneal syndrome Kaeser type","mesh","C566695"
> "0111551","neurogenic scapuloperoneal syndrome Kaeser type","umls","C1867005"
> "0111552","scapuloperoneal spinal muscular atrophy","umls","C0751335"
> "10159","osteonecrosis","icd10cm","M87"
> "10159","osteonecrosis","icd10cm","M87.9"
> "10159","osteonecrosis","icd9cm","732.3"
> "10159","osteonecrosis","icd9cm","733.41"
> "10159","osteonecrosis","icd9cm","733.42"
> "10159","osteonecrosis","icd9cm","733.43"
> "10159","osteonecrosis","icd9cm","733.44"
> "10159","osteonecrosis","mesh","D010020"
> "10159","osteonecrosis","umls","C0003977"
> "10159","osteonecrosis","umls","C0027543"
> "10159","osteonecrosis","umls","C0029445"
> "10159","osteonecrosis","umls","C0158442"
> "10159","osteonecrosis","umls","C0158449"
> "10159","osteonecrosis","umls","C0158450"
> "10159","osteonecrosis","umls","C0158451"
> "10159","osteonecrosis","umls","C0745048"
> "10159","osteonecrosis","mondo","0005380"
> "9339","urethral false passage","icd10cm","N36.5"
> "9339","urethral false passage","icd9cm","599.4"
> "9339","urethral false passage","umls","C0156286"
> "9339","urethral false passage","mondo","0004760"
> "0070252","autosomal dominant Emery-Dreifuss muscular dystrophy 7","mondo","0013677"
> "0070255","congenital disorder of glycosylation type IIc","umls","C0398739"
> "0070255","congenital disorder of glycosylation type IIc","mondo","0009953"
> "9621","non-congenital cyst of kidney","icd10cm","N28.1"
> "9621","non-congenital cyst of kidney","icd9cm","593.2"
> "9621","non-congenital cyst of kidney","umls","C0268799"
> "9621","non-congenital cyst of kidney","mondo","0004840"
> "9620","vesicoureteral reflux","icd10cm","N13.7"
> "9620","vesicoureteral reflux","icd10cm","N13.70"
> "9620","vesicoureteral reflux","icd9cm","593.7"
> "9620","vesicoureteral reflux","mesh","D014718"
> "9620","vesicoureteral reflux","umls","C0042580"
> "9620","vesicoureteral reflux","mondo","0006007"
> "1508","candidiasis","icd10cm","B37"
> "1508","candidiasis","icd10cm","B37.9"
> "1508","candidiasis","icd9cm","112"
> "1508","candidiasis","icd9cm","112.9"
> "1508","candidiasis","mesh","D002177"
> "1508","candidiasis","umls","C0006840"
> "1508","candidiasis","mondo","0002026"
> "9297","lip disease","icd10cm","K13.0"
> "9297","lip disease","icd9cm","528.5"
> "9297","lip disease","mesh","D008047"
> "9297","lip disease","umls","C0023760"
> "9297","lip disease","mondo","0004748"
> "1509","avoidant personality disorder","icd10cm","F60.6"
> "1509","avoidant personality disorder","icd9cm","301.82"
> "1509","avoidant personality disorder","mesh","D010554"
> "1509","avoidant personality disorder","umls","C0004444"
> "1509","avoidant personality disorder","mondo","0002027"
> "1975","thymus lipoma","umls","C1336744"
> "1975","thymus lipoma","mondo","0002163"
> "1974","adenosarcoma","mesh","D018195"
> "1974","adenosarcoma","umls","C0001442"
> "1974","adenosarcoma","mondo","0005636"
> "14096","infertility due to extratesticular cause","icd9cm","606.8"
> "14096","infertility due to extratesticular cause","umls","C0021360"
> "14096","infertility due to extratesticular cause","mondo","0001877"
> "14095","boutonneuse fever","icd10cm","A77.1"
> "14095","boutonneuse fever","icd9cm","082.1"
> "14095","boutonneuse fever","mesh","D001907"
> "14095","boutonneuse fever","umls","C0006060"
> "14095","boutonneuse fever","mondo","0024472"
> "14092","renal artery atheroma","icd10cm","I70.1"
> "14092","renal artery atheroma","icd9cm","440.1"
> "14092","renal artery atheroma","umls","C0155734"
> "14092","renal artery atheroma","mondo","0001876"
> "1970","fallopian tube carcinosarcoma","umls","C1517117"
> "1970","fallopian tube carcinosarcoma","mondo","0006207"
> "14099","acquired gastric outlet stenosis","icd9cm","537.0"
> "14099","acquired gastric outlet stenosis","umls","C0700588"
> "14099","acquired gastric outlet stenosis","mondo","0001878"
> "0111565","trichodontoosseous syndrome","mesh","C536549"
> "0111565","trichodontoosseous syndrome","umls","C0265333"
> "3230","high pressure neurological syndrome","mesh","D006610"
> "3230","high pressure neurological syndrome","umls","C0019537"
> "3230","high pressure neurological syndrome","mondo","0002570"
> "5199","ureteral obstruction","icd9cm","593.4"
> "5199","ureteral obstruction","mesh","D014517"
> "5199","ureteral obstruction","umls","C0029866"
> "5199","ureteral obstruction","mondo","0003329"
> "1969","cerebral palsy","icd10cm","G80"
> "1969","cerebral palsy","icd10cm","G80.9"
> "1969","cerebral palsy","mesh","D002547"
> "1969","cerebral palsy","umls","C0007789"
> "1969","cerebral palsy","mondo","0006497"
> "1618","breast fibroadenoma","icd10cm","D24"
> "1618","breast fibroadenoma","mesh","D018226"
> "1618","breast fibroadenoma","umls","C0178421"
> "1618","breast fibroadenoma","umls","C0206650"
> "1618","breast fibroadenoma","umls","C0346158"
> "1618","breast fibroadenoma","umls","C1333137"
> "1618","breast fibroadenoma","mondo","0002056"
> "0111564","hypoplastic or aplastic tibia with polydactyly","mesh","C535564"
> "0111564","hypoplastic or aplastic tibia with polydactyly","umls","C1861099"
> "1964","fallopian tube cancer","icd10cm","C57.0"
> "1964","fallopian tube cancer","icd9cm","183.2"
> "1964","fallopian tube cancer","mesh","D005185"
> "1964","fallopian tube cancer","umls","C0015558"
> "1964","fallopian tube cancer","umls","C0153579"
> "1964","fallopian tube cancer","mondo","0002158"
> "5194","intermixed schwannian stroma-rich ganglioneuroblastoma","umls","C1517444"
> "5194","intermixed schwannian stroma-rich ganglioneuroblastoma","mondo","0003326"
> "1614","male breast cancer","mesh","D018567"
> "1614","male breast cancer","umls","C0242788"
> "1614","male breast cancer","mondo","0005628"
> "1967","leiomyosarcoma","mesh","D007890"
> "1967","leiomyosarcoma","umls","C0023269"
> "1967","leiomyosarcoma","mondo","0005058"
> "1612","breast cancer","icd10cm","C50"
> "1612","breast cancer","icd10cm","C50-C50"
> "1612","breast cancer","mesh","D001943"
> "1612","breast cancer","umls","C0006142"
> "1612","breast cancer","mondo","0007254"
> "5190","cervical Wilms' tumor","umls","C1516437"
> "5190","cervical Wilms' tumor","mondo","0006144"
> "1962","fallopian tube disease","mesh","D005184"
> "1962","fallopian tube disease","umls","C0015556"
> "1962","fallopian tube disease","mondo","0002156"
> "0080011","bone resorption disease","mesh","D001862"
> "0080011","bone resorption disease","mondo","0000837"
> "0111561","stiff skin syndrome","mesh","C566112"
> "0111561","stiff skin syndrome","umls","C1861456"
> "13269","hereditary coproporphyria","icd10cm","E80.29"
> "13269","hereditary coproporphyria","mesh","D046349"
> "13269","hereditary coproporphyria","umls","C0162531"
> "13269","hereditary coproporphyria","mondo","0007369"
> "13268","porphyria","icd10cm","E80.20"
> "13268","porphyria","icd9cm","277.1"
> "13268","porphyria","mesh","D011164"
> "13268","porphyria","umls","C0032708"
> "13268","porphyria","mondo","0019142"
> "0110207","Charcot-Marie-Tooth disease X-linked dominant 6","icd10cm","G60.0"
> "0110207","Charcot-Marie-Tooth disease X-linked dominant 6","mondo","0010479"
> "0110206","Charcot-Marie-Tooth disease dominant intermediate F","icd10cm","G60.0"
> "0110206","Charcot-Marie-Tooth disease dominant intermediate F","mondo","0014074"
> "2871","endometrial carcinoma","mesh","D016889"
> "2871","endometrial carcinoma","mesh","D018269"
> "2871","endometrial carcinoma","umls","C0206687"
> "2871","endometrial carcinoma","umls","C0476089"
> "2871","endometrial carcinoma","mondo","0002447"
> "2870","endometrial adenocarcinoma","umls","C0279763"
> "2870","endometrial adenocarcinoma","umls","C1153706"
> "2870","endometrial adenocarcinoma","umls","C1336905"
> "2870","endometrial adenocarcinoma","mondo","0005461"
> "2877","larynx sarcoma","umls","C1334377"
> "2877","larynx sarcoma","mondo","0002448"
> "2876","laryngeal squamous cell carcinoma","umls","C0280324"
> "2876","laryngeal squamous cell carcinoma","mondo","0005595"
> "0110201","Charcot-Marie-Tooth disease recessive intermediate A","mondo","0012014"
> "0110200","Charcot-Marie-Tooth disease dominant intermediate D","icd10cm","G60.0"
> "0110200","Charcot-Marie-Tooth disease dominant intermediate D","mondo","0011909"
> "2879","nodular degeneration of cornea","icd10cm","H18.45"
> "2879","nodular degeneration of cornea","icd9cm","371.46"
> "2879","nodular degeneration of cornea","umls","C0155122"
> "2879","nodular degeneration of cornea","mondo","0002449"
> "0110569","autosomal dominant nonsyndromic deafness 44","icd10cm","H90.3"
> "0110569","autosomal dominant nonsyndromic deafness 44","mondo","0011832"
> "0110209","Charcot-Marie-Tooth disease X-linked dominant 1","icd10cm","G60.0"
> "0110209","Charcot-Marie-Tooth disease X-linked dominant 1","mondo","0010549"
> "0110208","Charcot-Marie-Tooth disease X-linked recessive 2","icd10cm","G60.0"
> "0110208","Charcot-Marie-Tooth disease X-linked recessive 2","mondo","0010550"
> "3355","fibrosarcoma","mesh","D005354"
> "3355","fibrosarcoma","mesh","D018218"
> "3355","fibrosarcoma","umls","C0016057"
> "3355","fibrosarcoma","umls","C0206643"
> "3355","fibrosarcoma","umls","C1336021"
> "3355","fibrosarcoma","mondo","0005164"
> "14272","pericholangitis","umls","C0031052"
> "14272","pericholangitis","mondo","0001931"
> "3357","extraosseous osteosarcoma","umls","C0855052"
> "3357","extraosseous osteosarcoma","mondo","0002621"
> "3356","localized osteosarcoma","umls","C0278511"
> "3356","localized osteosarcoma","mondo","0002620"
> "3351","bone angioendothelial sarcoma","umls","C1332574"
> "3351","bone angioendothelial sarcoma","mondo","0002617"
> "3350","mesenchymal cell neoplasm","umls","C1332517"
> "3350","mesenchymal cell neoplasm","umls","C1334699"
> "3350","mesenchymal cell neoplasm","mondo","0002616"
> "14275","atrophic vulva","icd10cm","N90.5"
> "14275","atrophic vulva","icd9cm","624.1"
> "14275","atrophic vulva","umls","C0156393"
> "14275","atrophic vulva","mondo","0001932"
> "3352","malignant fibrous histiocytoma of bone","umls","C0740479"
> "3352","malignant fibrous histiocytoma of bone","mondo","0002618"
> "5443","clear cell hidradenoma","umls","C1370701"
> "5443","clear cell hidradenoma","mondo","0003447"
> "5442","eccrine acrospiroma","mesh","D018250"
> "5442","eccrine acrospiroma","umls","C0206671"
> "5442","eccrine acrospiroma","mondo","0006738"
> "2544","extratemporal epilepsy","umls","C0270849"
> "2544","extratemporal epilepsy","mondo","0002338"
> "5446","eccrine papillary adenoma","umls","C0334350"
> "5446","eccrine papillary adenoma","mondo","0003450"
> "5445","syringocystadenoma papilliferum","mesh","D000074009"
> "5445","syringocystadenoma papilliferum","umls","C0406803"
> "5445","syringocystadenoma papilliferum","mondo","0019392"
> "5444","spiradenoma","umls","C0334347"
> "5444","spiradenoma","mondo","0003448"
> "5508","brain stem ependymoma","umls","C1332609"
> "5508","brain stem ependymoma","mondo","0003477"
> "5509","pediatric ependymoma","mondo","0003478"
> "5504","tanycytic ependymoma","umls","C1370500"
> "5504","tanycytic ependymoma","mondo","0003474"
> "5505","papillary ependymoma","mesh","D004806"
> "5505","papillary ependymoma","umls","C0334578"
> "5505","papillary ependymoma","mondo","0003475"
> "5502","lice infestation","icd10cm","B85.2"
> "5502","lice infestation","icd9cm","132.9"
> "5502","lice infestation","mesh","D010373"
> "5502","lice infestation","umls","C0030756"
> "5502","lice infestation","mondo","0003472"
> "5503","spinal cord ependymoma","umls","C0238432"
> "5503","spinal cord ependymoma","mondo","0003473"
> "5500","cellular ependymoma","mesh","D004806"
> "5500","cellular ependymoma","umls","C1384403"
> "5500","cellular ependymoma","mondo","0003470"
> "5501","Pediculus humanus capitis infestation","icd10cm","B85.0"
> "5501","Pediculus humanus capitis infestation","icd9cm","132.0"
> "5501","Pediculus humanus capitis infestation","umls","C0030757"
> "5501","Pediculus humanus capitis infestation","mondo","0003471"
> "0110212","Charcot-Marie-Tooth disease X-linked recessive 4","icd10cm","G60.0"
> "0110212","Charcot-Marie-Tooth disease X-linked recessive 4","mondo","0010689"
> "12798","mucopolysaccharidosis","icd10cm","E76.3"
> "12798","mucopolysaccharidosis","icd9cm","277.5"
> "12798","mucopolysaccharidosis","mesh","D009083"
> "12798","mucopolysaccharidosis","umls","C0026703"
> "12798","mucopolysaccharidosis","mondo","0019249"
> "543","dystonia","icd10cm","G24"
> "543","dystonia","icd10cm","G24.9"
> "543","dystonia","mesh","D004421"
> "543","dystonia","mesh","D020821"
> "543","dystonia","umls","C0013421"
> "543","dystonia","umls","C0393593"
> "543","dystonia","mondo","0003441"
> "540","strabismus","icd10cm","H50.8"
> "540","strabismus","icd10cm","H50.89"
> "540","strabismus","icd9cm","378.7"
> "540","strabismus","mesh","D013285"
> "540","strabismus","umls","C0029831"
> "540","strabismus","mondo","0003432"
> "12799","mucopolysaccharidosis II","icd10cm","E76.1"
> "12799","mucopolysaccharidosis II","mesh","D016532"
> "12799","mucopolysaccharidosis II","umls","C0026705"
> "12799","mucopolysaccharidosis II","mondo","0010674"
> "0110218","Brugada syndrome 1","icd10cm","I49.8"
> "0110218","Brugada syndrome 1","mondo","0011001"
> "0110219","Brugada syndrome 2","icd10cm","I49.8"
> "0110219","Brugada syndrome 2","mondo","0012728"
> "3320","Tay-Sachs disease","icd10cm","E75.02"
> "3320","Tay-Sachs disease","mesh","D013661"
> "3320","Tay-Sachs disease","umls","C0039373"
> "3320","Tay-Sachs disease","mondo","0010100"
> "6569","micropapillomatosis labialis","umls","C1519982"
> "6569","micropapillomatosis labialis","mondo","0003929"
> "3321","GM2 gangliosidosis","icd10cm","E75.0"
> "3321","GM2 gangliosidosis","icd10cm","E75.00"
> "3321","GM2 gangliosidosis","mesh","D020143"
> "3321","GM2 gangliosidosis","umls","C0268274"
> "3321","GM2 gangliosidosis","mondo","0017720"
> "6564","neurilemmoma of the pleura","umls","C1335435"
> "6564","neurilemmoma of the pleura","mondo","0003926"
> "6567","uterine corpus myxoid leiomyosarcoma","umls","C1519861"
> "6567","uterine corpus myxoid leiomyosarcoma","mondo","0003928"
> "6566","posterior uveal melanoma","umls","C0278867"
> "6566","posterior uveal melanoma","umls","C0278868"
> "6566","posterior uveal melanoma","mondo","0003927"
> "3322","GM1 gangliosidosis","icd10cm","E75.19"
> "3322","GM1 gangliosidosis","mesh","D016537"
> "3322","GM1 gangliosidosis","umls","C0085131"
> "3322","GM1 gangliosidosis","mondo","0018149"
> "6562","ethmoid sinus inverted papilloma","umls","C1333474"
> "6562","ethmoid sinus inverted papilloma","mondo","0003925"
> "7685","pancreatic non-invasive intraductal papillary-mucinous carcinoma","umls","C1518873"
> "7685","pancreatic non-invasive intraductal papillary-mucinous carcinoma","mondo","0004329"
> "5475","uterine corpus adenofibroma","umls","C1336901"
> "5475","uterine corpus adenofibroma","mondo","0003458"
> "14268","sclerosing cholangitis","icd10cm","K83.0"
> "14268","sclerosing cholangitis","mesh","D015209"
> "14268","sclerosing cholangitis","umls","C0008313"
> "14268","sclerosing cholangitis","mondo","0018646"
> "7689","leptomeninges sarcoma","umls","C1384416"
> "7689","leptomeninges sarcoma","mondo","0004330"
> "14269","suppurative cholangitis","icd10cm","K83.0"
> "14269","suppurative cholangitis","umls","C0267924"
> "14269","suppurative cholangitis","mondo","0001928"
> "3827","congenital diaphragmatic hernia","icd10cm","K44"
> "3827","congenital diaphragmatic hernia","icd10cm","K44.9"
> "3827","congenital diaphragmatic hernia","mesh","D006548"
> "3827","congenital diaphragmatic hernia","umls","C0019284"
> "3827","congenital diaphragmatic hernia","mondo","0005711"
> "0070116","Meckel syndrome 2","icd10cm","Q61.9"
> "0070116","Meckel syndrome 2","mondo","0011296"
> "3825","Shwartzman phenomenon","mesh","D012790"
> "3825","Shwartzman phenomenon","umls","C0037018"
> "3825","Shwartzman phenomenon","mondo","0002783"
> "3821","posterior cerebral artery infarction","mesh","D020762"
> "3821","posterior cerebral artery infarction","umls","C0752132"
> "3821","posterior cerebral artery infarction","mondo","0006917"
> "2769","tic disorder","icd10cm","F95"
> "2769","tic disorder","icd10cm","F95.9"
> "2769","tic disorder","icd9cm","307.2"
> "2769","tic disorder","icd9cm","307.20"
> "2769","tic disorder","mesh","D013981"
> "2769","tic disorder","umls","C0040188"
> "2769","tic disorder","mondo","0002420"
> "3829","pituitary adenoma","mesh","D010911"
> "3829","pituitary adenoma","umls","C0032000"
> "3829","pituitary adenoma","mondo","0006373"
> "3828","chromophobe adenoma","mesh","D000238"
> "3828","chromophobe adenoma","umls","C0001432"
> "3828","chromophobe adenoma","mondo","0006701"
> "8445","intestinal volvulus","icd10cm","K56.2"
> "8445","intestinal volvulus","icd9cm","560.2"
> "8445","intestinal volvulus","mesh","D045822"
> "8445","intestinal volvulus","umls","C0042961"
> "8445","intestinal volvulus","mondo","0004570"
> "8446","intussusception","icd10cm","K56.1"
> "8446","intussusception","icd9cm","560.0"
> "8446","intussusception","mesh","D007443"
> "8446","intussusception","umls","C0021933"
> "8446","intussusception","mondo","0007835"
> "2768","transient tic disorder","icd10cm","F95.0"
> "2768","transient tic disorder","icd9cm","307.21"
> "2768","transient tic disorder","mesh","D013981"
> "2768","transient tic disorder","umls","C0040702"
> "2768","transient tic disorder","mondo","0002419"
> "8440","ileus","mesh","D045823"
> "8440","ileus","umls","C1258215"
> "8440","ileus","mondo","0004567"
> "8442","paralytic ileus","icd10cm","K56.0"
> "8442","paralytic ileus","icd9cm","560.1"
> "8442","paralytic ileus","mesh","D007418"
> "8442","paralytic ileus","umls","C0030446"
> "8442","paralytic ileus","mondo","0004568"
> "8443","brachial plexus lesion","icd9cm","353.0"
> "8443","brachial plexus lesion","umls","C0006091"
> "8443","brachial plexus lesion","mondo","0004569"
> "8448","intestinal impaction","icd10cm","K56.4"
> "8448","intestinal impaction","icd10cm","K56.49"
> "8448","intestinal impaction","icd9cm","560.39"
> "8448","intestinal impaction","umls","C0029640"
> "8448","intestinal impaction","mondo","0004571"
> "10337","glaucomatous atrophy of optic disc","icd10cm","H47.23"
> "10337","glaucomatous atrophy of optic disc","icd9cm","377.14"
> "10337","glaucomatous atrophy of optic disc","umls","C0271342"
> "10337","glaucomatous atrophy of optic disc","mondo","0001006"
> "0060027","agammaglobulinemia 4","mondo","0000584"
> "0060025","immunoglobulin alpha deficiency","mesh","D017098"
> "0060025","immunoglobulin alpha deficiency","umls","C0162538"
> "0060025","immunoglobulin alpha deficiency","mondo","0001341"
> "7539","pregnancy adenoma","umls","C1266023"
> "7539","pregnancy adenoma","mondo","0004271"
> "7538","breast ductal adenoma","umls","C1511307"
> "7538","breast ductal adenoma","mondo","0004270"
> "368","cerebrum cancer","icd9cm","191.8"
> "368","cerebrum cancer","umls","C0153642"
> "368","cerebrum cancer","umls","C1263885"
> "368","cerebrum cancer","mondo","0002731"
> "369","olfactory neuroblastoma","mesh","D018304"
> "369","olfactory neuroblastoma","umls","C0206717"
> "369","olfactory neuroblastoma","mondo","0006329"
> "366","olfactory nerve neoplasm","umls","C0346319"
> "366","olfactory nerve neoplasm","mondo","0002722"
> "367","olfactory nerve disease","icd10cm","G52.0"
> "367","olfactory nerve disease","icd9cm","352.0"
> "367","olfactory nerve disease","mesh","D020431"
> "367","olfactory nerve disease","umls","C0751937"
> "367","olfactory nerve disease","mondo","0002727"
> "365","bladder disease","icd10cm","N32.9"
> "365","bladder disease","icd9cm","596.9"
> "365","bladder disease","mesh","D001745"
> "365","bladder disease","umls","C0005686"
> "365","bladder disease","mondo","0006026"
> "7531","anal gland adenocarcinoma","umls","C1266027"
> "7531","anal gland adenocarcinoma","mondo","0004266"
> "363","uterine cancer","icd10cm","C55"
> "363","uterine cancer","icd9cm","179"
> "363","uterine cancer","mesh","D014594"
> "363","uterine cancer","umls","C0042138"
> "363","uterine cancer","umls","C0153567"
> "363","uterine cancer","mondo","0002715"
> "7533","subareolar duct papillomatosis","mondo","0004268"
> "361","cervix endometriosis","umls","C0269107"
> "361","cervix endometriosis","mondo","0002706"
10272,10288c19962,20124
< "0110411","retinitis pigmentosa 60","icd10cm","H35.5"
< "0110411","retinitis pigmentosa 60","mondo","0013516"
< "0060759","immunodeficiency with hyper IgM type 5","icd10cm","D80.5"
< "0060759","immunodeficiency with hyper IgM type 5","mondo","0011971"
< "4914","esophagus adenocarcinoma","mesh","C562730"
< "4914","esophagus adenocarcinoma","umls","C0279628"
< "4914","esophagus adenocarcinoma","mondo","0005028"
< "13403","neurosarcoidosis","umls","C0398676"
< "13403","neurosarcoidosis","mondo","0001706"
< "0110842","Usher syndrome type 3B","icd10cm","H35.5"
< "0110842","Usher syndrome type 3B","mondo","0013788"
< "0090132","complex cortical dysplasia with other brain malformations 7","icd10cm","Q04.3"
< "0090132","complex cortical dysplasia with other brain malformations 7","mondo","0012399"
< "4661","multiple chemical sensitivity","mesh","D018777"
< "4661","multiple chemical sensitivity","umls","C0242992"
< "4661","multiple chemical sensitivity","mondo","0005862"
< "0110706","hypotrichosis 9","mondo","0013649"
---
> "6179","ovarian small cell carcinoma","mondo","0003795"
> "6175","mediastinal neurilemmoma","umls","C1334679"
> "6175","mediastinal neurilemmoma","mondo","0004398"
> "6170","ovarian carcinosarcoma","umls","C0392998"
> "6170","ovarian carcinosarcoma","mondo","0003792"
> "6171","uterine carcinosarcoma","umls","C0280630"
> "6171","uterine carcinosarcoma","mondo","0006485"
> "10989","conjunctival vascular disease","icd10cm","H11.41"
> "10989","conjunctival vascular disease","icd9cm","372.74"
> "10989","conjunctival vascular disease","umls","C0042370"
> "10989","conjunctival vascular disease","mondo","0001174"
> "7401","colonic L-cell glucagon-like peptide producing tumor","umls","C3274139"
> "7401","colonic L-cell glucagon-like peptide producing tumor","mondo","0004210"
> "10986","discitis","icd10cm","M46.4"
> "10986","discitis","mesh","D015299"
> "10986","discitis","umls","C0012624"
> "10986","discitis","mondo","0006728"
> "10983","Alport syndrome","mesh","D009394"
> "10983","Alport syndrome","umls","C0027706"
> "10983","Alport syndrome","mondo","0018965"
> "7400","Nijmegen breakage syndrome","mesh","D049932"
> "7400","Nijmegen breakage syndrome","umls","C0398791"
> "7400","Nijmegen breakage syndrome","mondo","0009623"
> "0050723","PSAT deficiency","mondo","0012596"
> "0050722","PHGDH deficiency","mesh","C566618"
> "0050722","PHGDH deficiency","mondo","0011152"
> "0050720","ornithine translocase deficiency","mondo","0009393"
> "0050727","tyrosinemia type III","mondo","0010162"
> "0050726","tyrosinemia type I","mondo","0010161"
> "0050725","tyrosinemia type II","mondo","0010160"
> "0050724","PSPH deficiency","mondo","0013531"
> "0050729","neutral lipid storage disease","mondo","0015611"
> "0080139","multiple congenital anomalies-hypotonia-seizures syndrome 2","mondo","0010466"
> "0080138","multiple congenital anomalies-hypotonia-seizures syndrome 1","mondo","0013563"
> "0080137","multiple endocrine neoplasia type 4","mondo","0012552"
> "0080136","multiple mitochondrial dysfunctions syndrome 4","mondo","0014611"
> "0080135","multiple mitochondrial dysfunctions syndrome 3","mondo","0014132"
> "0080134","multiple mitochondrial dysfunctions syndrome 2","mondo","0013675"
> "0080133","multiple mitochondrial dysfunctions syndrome 1","mondo","0011582"
> "0080132","Sengers syndrome","mesh","C538280"
> "0080132","Sengers syndrome","mondo","0008922"
> "0080131","mitochondrial DNA depletion syndrome 13","mondo","0014198"
> "0080130","mitochondrial DNA depletion syndrome 12a","mondo","0014175"
> "0111033","African iron overload","icd10cm","E83.1"
> "0111033","African iron overload","mondo","0011012"
> "0111032","hemochromatosis type 2B","mondo","0013220"
> "0111031","hemochromatosis type 5","icd10cm","E83.1"
> "0111031","hemochromatosis type 5","mondo","0014225"
> "0111030","hemochromatosis type 3","mesh","C537248"
> "0111030","hemochromatosis type 3","umls","C1858664"
> "0111030","hemochromatosis type 3","mondo","0011417"
> "0111037","glycine N-methyltransferase deficiency","icd10cm","E72.1"
> "0111037","glycine N-methyltransferase deficiency","mondo","0011698"
> "0111036","CADASIL 2","icd10cm","F01.1"
> "0111036","CADASIL 2","mondo","0014768"
> "0111035","CADASIL 1","icd10cm","F01.1"
> "0111035","CADASIL 1","mondo","0000914"
> "0111034","hemochromatosis type 2","icd10cm","E83.1"
> "0111034","hemochromatosis type 2","mesh","C537247"
> "0111034","hemochromatosis type 2","mondo","0019257"
> "0111039","hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase","icd10cm","E72.1"
> "0111039","hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase","mondo","0013404"
> "0111038","hypermethioninemia due to adenosine kinase deficiency","icd10cm","E72.1"
> "0111038","hypermethioninemia due to adenosine kinase deficiency","mondo","0013676"
> "11581","phlyctenulosis","icd10cm","H16.25"
> "11581","phlyctenulosis","icd9cm","370.31"
> "11581","phlyctenulosis","umls","C0155080"
> "11581","phlyctenulosis","mondo","0001317"
> "11589","Riley-Day syndrome","icd10cm","G90.1"
> "11589","Riley-Day syndrome","mesh","D004402"
> "11589","Riley-Day syndrome","umls","C0013364"
> "11589","Riley-Day syndrome","mondo","0009131"
> "12241","beta thalassemia","icd10cm","D56.1"
> "12241","beta thalassemia","icd9cm","282.44"
> "12241","beta thalassemia","mesh","D017086"
> "12241","beta thalassemia","umls","C0005283"
> "12241","beta thalassemia","mondo","0019402"
> "4428","dyslexia","icd10cm","F81.0"
> "4428","dyslexia","mesh","D004410"
> "4428","dyslexia","umls","C0476254"
> "4428","dyslexia","mondo","0005489"
> "0080353","X-linked recessive hypophosphatemic rickets","mondo","0010358"
> "0080352","X-linked chondrodysplasia punctata 2","mondo","0020603"
> "0080351","CLOVES syndrome","icd10cm","Q87.3"
> "0080351","CLOVES syndrome","mondo","0013038"
> "0080350","retinitis pigmentosa 77","icd10cm","H35.5"
> "0080350","retinitis pigmentosa 77","mondo","0015013"
> "4839","sebaceous adenocarcinoma","mesh","D018266"
> "4839","sebaceous adenocarcinoma","umls","C0206684"
> "4839","sebaceous adenocarcinoma","mondo","0006962"
> "4838","myoepithelial carcinoma","umls","C0334699"
> "4838","myoepithelial carcinoma","mondo","0003158"
> "4527","ovarian angiosarcoma","umls","C1335152"
> "4527","ovarian angiosarcoma","mondo","0003035"
> "4830","adenosquamous carcinoma","mesh","D018196"
> "4830","adenosquamous carcinoma","umls","C0206623"
> "4830","adenosquamous carcinoma","mondo","0006074"
> "4525","mediastinum angiosarcoma","umls","C1334649"
> "4525","mediastinum angiosarcoma","mondo","0003034"
> "4524","prostate angiosarcoma","umls","C1335504"
> "4524","prostate angiosarcoma","mondo","0003033"
> "13452","scleritis","icd10cm","H15.0"
> "13452","scleritis","icd10cm","H15.00"
> "13452","scleritis","icd9cm","379.00"
> "13452","scleritis","mesh","D015423"
> "13452","scleritis","umls","C0036416"
> "13452","scleritis","mondo","0001718"
> "4522","superior vena cava angiosarcoma","umls","C1336530"
> "4522","superior vena cava angiosarcoma","mondo","0003032"
> "4521","cervix endometrial stromal tumor","umls","C4289586"
> "4521","cervix endometrial stromal tumor","mondo","0003031"
> "4520","cervical endometrial stromal sarcoma","umls","C3642326"
> "4520","cervical endometrial stromal sarcoma","mondo","0003030"
> "13333","hypertrophy of tongue papillae","icd10cm","K14.3"
> "13333","hypertrophy of tongue papillae","icd9cm","529.3"
> "13333","hypertrophy of tongue papillae","umls","C0392494"
> "13333","hypertrophy of tongue papillae","mondo","0001689"
> "7997","thyrotoxicosis","icd10cm","E05.9"
> "7997","thyrotoxicosis","icd9cm","242"
> "7997","thyrotoxicosis","mesh","D013971"
> "7997","thyrotoxicosis","umls","C0040156"
> "7997","thyrotoxicosis","mondo","0010138"
> "7996","familial glomangioma","umls","C1333987"
> "7996","familial glomangioma","mondo","0004424"
> "7994","central nervous system osteosarcoma","umls","C1335150"
> "7994","central nervous system osteosarcoma","mondo","0004423"
> "11634","myxedema","icd10cm","E03.9"
> "11634","myxedema","mesh","D009230"
> "11634","myxedema","umls","C0027145"
> "11634","myxedema","mondo","0009718"
> "7998","hyperthyroidism","icd10cm","E05.9"
> "7998","hyperthyroidism","mesh","D006980"
> "7998","hyperthyroidism","umls","C0020550"
> "7998","hyperthyroidism","mondo","0004425"
> "9432","renal glycosuria","icd10cm","E74.8"
> "9432","renal glycosuria","icd9cm","271.4"
> "9432","renal glycosuria","mesh","D006030"
> "9432","renal glycosuria","umls","C0017980"
> "9432","renal glycosuria","mondo","0009297"
> "11633","thyroid hormone resistance syndrome","mesh","D018382"
> "11633","thyroid hormone resistance syndrome","umls","C2940786"
> "11633","thyroid hormone resistance syndrome","mondo","0001328"
> "5299","endometrial clear cell adenocarcinoma","umls","C0279765"
> "5299","endometrial clear cell adenocarcinoma","mondo","0006191"
> "5296","liver leiomyosarcoma","umls","C1333969"
> "5296","liver leiomyosarcoma","mondo","0003378"
> "5297","rectum leiomyosarcoma","umls","C1335683"
> "5297","rectum leiomyosarcoma","mondo","0003379"
> "5295","intestinal disease","icd10cm","K63.9"
> "5295","intestinal disease","icd9cm","569.9"
> "5295","intestinal disease","mesh","D007410"
> "5295","intestinal disease","umls","C0021831"
> "5295","intestinal disease","mondo","0005020"
> "5292","mediastinum leiomyosarcoma","umls","C1334660"
> "5292","mediastinum leiomyosarcoma","mondo","0003376"
> "5293","extrahepatic bile duct leiomyosarcoma","umls","C1333508"
> "5293","extrahepatic bile duct leiomyosarcoma","mondo","0003377"
> "13185","esophageal diverticulosis","mesh","D045723"
> "13185","esophageal diverticulosis","umls","C0917875"
> "13185","esophageal diverticulosis","mondo","0006754"
> "13186","megaesophagus","mesh","D004931"
> "13186","megaesophagus","umls","C0025164"
> "13186","megaesophagus","mondo","0001656"
10300,10305c20136,24547
< "0110846","xeroderma pigmentosum group E","icd10cm","Q82.1"
< "0110846","xeroderma pigmentosum group E","mondo","0010213"
< "4653","intraocular retinoblastoma","umls","C0278717"
< "4653","intraocular retinoblastoma","mondo","0003077"
< "6621","cerebral angioma","umls","C0877388"
< "6621","cerebral angioma","mondo","0003948"
---
> "11809","bladder neck cancer","icd10cm","C67.5"
> "11809","bladder neck cancer","icd9cm","188.5"
> "11809","bladder neck cancer","umls","C0153613"
> "11809","bladder neck cancer","mondo","0001372"
> "0110782","hereditary spastic paraplegia 31","icd10cm","G11.4"
> "0110782","hereditary spastic paraplegia 31","mondo","0012453"
> "0110783","hereditary spastic paraplegia 32","icd10cm","G11.4"
> "0110783","hereditary spastic paraplegia 32","mondo","0012643"
> "0110780","hereditary spastic paraplegia 29","icd10cm","G11.4"
> "0110780","hereditary spastic paraplegia 29","mondo","0012334"
> "0110781","hereditary spastic paraplegia 30","icd10cm","G11.4"
> "0110781","hereditary spastic paraplegia 30","mondo","0012476"
> "0110786","hereditary spastic paraplegia 35","icd10cm","G11.4"
> "0110786","hereditary spastic paraplegia 35","mondo","0012866"
> "0110787","hereditary spastic paraplegia 36","icd10cm","G11.4"
> "0110787","hereditary spastic paraplegia 36","mondo","0013132"
> "0110784","hereditary spastic paraplegia 33","mondo","0012448"
> "0110785","hereditary spastic paraplegia 34","icd10cm","G11.4"
> "0110785","hereditary spastic paraplegia 34","mondo","0010418"
> "0110788","hereditary spastic paraplegia 37","icd10cm","G11.4"
> "0110788","hereditary spastic paraplegia 37","mondo","0012766"
> "0110789","hereditary spastic paraplegia 38","icd10cm","G11.4"
> "0110789","hereditary spastic paraplegia 38","mondo","0012867"
> "8635","uvula cancer","icd10cm","C05.2"
> "8635","uvula cancer","icd9cm","145.4"
> "8635","uvula cancer","umls","C0153377"
> "8635","uvula cancer","mondo","0004624"
> "6997","intermediate cell type ciliary body melanoma","umls","C1334209"
> "6997","intermediate cell type ciliary body melanoma","mondo","0004066"
> "8144","pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma","umls","C1333038"
> "8144","pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma","mondo","0004478"
> "6993","iris mixed cell melanoma","umls","C1334210"
> "6993","iris mixed cell melanoma","mondo","0004063"
> "0070251","X-linked Emery-Dreifuss muscular dystrophy 6","mondo","0010401"
> "0070250","autosomal dominant Emery-Dreifuss muscular dystrophy 5","mondo","0013072"
> "0070253","congenital disorder of glycosylation type IIa","umls","C2931008"
> "0070253","congenital disorder of glycosylation type IIa","mondo","0008908"
> "7334","nephrogenic adenoma","umls","C0334039"
> "7334","nephrogenic adenoma","mondo","0004191"
> "7333","nephrogenic adenoma of urinary bladder","umls","C1336892"
> "7333","nephrogenic adenoma of urinary bladder","mondo","0004190"
> "7332","esophageal tuberculosis","icd9cm","017.8"
> "7332","esophageal tuberculosis","umls","C0152902"
> "7332","esophageal tuberculosis","mondo","0004189"
> "0070257","congenital disorder of glycosylation type IIe","umls","C2931010"
> "0070257","congenital disorder of glycosylation type IIe","mondo","0010490"
> "0070256","congenital disorder of glycosylation type IId","umls","C2931009"
> "0070256","congenital disorder of glycosylation type IId","mondo","0011772"
> "0070259","congenital disorder of glycosylation type IIg","umls","C2931011"
> "0070259","congenital disorder of glycosylation type IIg","mondo","0012637"
> "0070258","congenital disorder of glycosylation type IIf","umls","C1970344"
> "0070258","congenital disorder of glycosylation type IIf","mondo","0011342"
> "9299","myocardium cancer","umls","C0346611"
> "9299","myocardium cancer","umls","C1290402"
> "9299","myocardium cancer","mondo","0004749"
> "0110568","autosomal dominant nonsyndromic deafness 43","icd10cm","H90.3"
> "0110568","autosomal dominant nonsyndromic deafness 43","mondo","0012030"
> "11963","esophagitis","icd10cm","K20"
> "11963","esophagitis","icd10cm","K20.9"
> "11963","esophagitis","icd9cm","530.1"
> "11963","esophagitis","icd9cm","530.10"
> "11963","esophagitis","mesh","D004941"
> "11963","esophagitis","umls","C0014868"
> "11963","esophagitis","mondo","0001409"
> "0110566","autosomal dominant nonsyndromic deafness 40","icd10cm","H90.3"
> "0110566","autosomal dominant nonsyndromic deafness 40","mondo","0014603"
> "0110567","autosomal dominant nonsyndromic deafness 41","icd10cm","H90.3"
> "0110567","autosomal dominant nonsyndromic deafness 41","mondo","0011994"
> "0110564","autosomal dominant nonsyndromic deafness 3A","icd10cm","H90.3"
> "0110564","autosomal dominant nonsyndromic deafness 3A","mondo","0011103"
> "0110565","autosomal dominant nonsyndromic deafness 3B","icd10cm","H90.3"
> "0110565","autosomal dominant nonsyndromic deafness 3B","mondo","0012975"
> "0110562","autosomal dominant nonsyndromic deafness 33","icd10cm","H90.3"
> "0110562","autosomal dominant nonsyndromic deafness 33","mondo","0013632"
> "0110563","autosomal dominant nonsyndromic deafness 36","icd10cm","H90.3"
> "0110563","autosomal dominant nonsyndromic deafness 36","mondo","0011708"
> "0110560","autosomal dominant nonsyndromic deafness 30","icd10cm","H90.3"
> "0110560","autosomal dominant nonsyndromic deafness 30","mondo","0011673"
> "0110561","autosomal dominant nonsyndromic deafness 31","icd10cm","H90.3"
> "0110561","autosomal dominant nonsyndromic deafness 31","mondo","0012086"
> "12927","screw worm infectious disease","mesh","D012610"
> "12927","screw worm infectious disease","umls","C0036465"
> "12927","screw worm infectious disease","mondo","0005954"
> "12926","hypodermyiasis","mesh","D007000"
> "12926","hypodermyiasis","umls","C0020607"
> "12926","hypodermyiasis","mondo","0005805"
> "12929","endocardial fibroelastosis","icd10cm","I42.4"
> "12929","endocardial fibroelastosis","icd9cm","425.3"
> "12929","endocardial fibroelastosis","mesh","D004695"
> "12929","endocardial fibroelastosis","umls","C0014117"
> "12929","endocardial fibroelastosis","mondo","0009169"
> "10211","cholelithiasis","icd9cm","574.5"
> "10211","cholelithiasis","mesh","D002769"
> "10211","cholelithiasis","umls","C0006739"
> "10211","cholelithiasis","mondo","0012672"
> "0060320","inguinal hernia","icd10cm","K40"
> "0060320","inguinal hernia","icd10cm","K40.90"
> "0060320","inguinal hernia","icd9cm","550"
> "0060320","inguinal hernia","mesh","D006552"
> "0060320","inguinal hernia","umls","C0019294"
> "0060320","inguinal hernia","umls","C0019295"
> "0060320","inguinal hernia","umls","C0019296"
> "0060320","inguinal hernia","mondo","0000746"
> "0060321","umbilical hernia","icd10cm","Q79.2"
> "0060321","umbilical hernia","icd9cm","756.72"
> "0060321","umbilical hernia","mesh","D006554"
> "0060321","umbilical hernia","umls","C0795690"
> "0060321","umbilical hernia","umls","C1306503"
> "0060321","umbilical hernia","mondo","0000747"
> "0060322","mastoiditis","icd10cm","H70.9"
> "0060322","mastoiditis","icd10cm","H70.90"
> "0060322","mastoiditis","icd9cm","383.9"
> "0060322","mastoiditis","mesh","D008417"
> "0060322","mastoiditis","umls","C0024904"
> "0060322","mastoiditis","mondo","0000748"
> "0060324","dental abscess","icd10cm","K04.6"
> "0060324","dental abscess","mondo","0000750"
> "0060325","cervical polyp","icd10cm","D26"
> "0060325","cervical polyp","icd10cm","D26.9"
> "0060325","cervical polyp","icd9cm","219"
> "0060325","cervical polyp","umls","C0153996"
> "0060325","cervical polyp","mondo","0000751"
> "0060326","myelomeningocele","icd10cm","Q05"
> "0060326","myelomeningocele","mesh","D008591"
> "0060326","myelomeningocele","umls","C0025312"
> "0060326","myelomeningocele","umls","C0086664"
> "0060326","myelomeningocele","umls","C0751316"
> "0060326","myelomeningocele","mondo","0019773"
> "0060327","omphalocele","icd10cm","Q79.2"
> "0060327","omphalocele","icd9cm","756.72"
> "0060327","omphalocele","mesh","D006554"
> "0060327","omphalocele","umls","C0795690"
> "0060327","omphalocele","umls","C1306503"
> "0060327","omphalocele","mondo","0019015"
> "0060328","anal fistula","icd10cm","K60.3"
> "0060328","anal fistula","mesh","D012003"
> "0060328","anal fistula","mondo","0000754"
> "0060329","ectopic pregnancy","icd10cm","O00"
> "0060329","ectopic pregnancy","icd10cm","O00.9"
> "0060329","ectopic pregnancy","icd10cm","O00.90"
> "0060329","ectopic pregnancy","icd9cm","633"
> "0060329","ectopic pregnancy","icd9cm","633.9"
> "0060329","ectopic pregnancy","mesh","D011271"
> "0060329","ectopic pregnancy","umls","C0032987"
> "0060329","ectopic pregnancy","mondo","0000755"
> "7050","thymus basaloid carcinoma","umls","C1332464"
> "7050","thymus basaloid carcinoma","mondo","0004092"
> "7051","esophageal basaloid squamous cell carcinoma","umls","C1333443"
> "7051","esophageal basaloid squamous cell carcinoma","mondo","0004093"
> "7054","multiple skull base meningioma","umls","C1334829"
> "7054","multiple skull base meningioma","mondo","0004094"
> "8149","malignant childhood germ cell neoplasm","umls","C1334574"
> "8149","malignant childhood germ cell neoplasm","mondo","0004479"
> "6998","gallbladder mucinous carcinoma","umls","C1333750"
> "6998","gallbladder mucinous carcinoma","mondo","0004067"
> "6994","malignant iris melanoma","umls","C0346373"
> "6994","malignant iris melanoma","mondo","0004064"
> "8140","adrenal gland ganglioneuroblastoma","umls","C1332176"
> "8140","adrenal gland ganglioneuroblastoma","mondo","0004477"
> "6996","intermediate cell type choroid melanoma","umls","C1334208"
> "6996","intermediate cell type choroid melanoma","mondo","0004065"
> "8634","prostate carcinoma in situ","icd10cm","D07.5"
> "8634","prostate carcinoma in situ","icd9cm","233.4"
> "8634","prostate carcinoma in situ","umls","C0154088"
> "8634","prostate carcinoma in situ","mondo","0004623"
> "8633","chronic intestinal vascular insufficiency","icd9cm","557.1"
> "8633","chronic intestinal vascular insufficiency","umls","C0311262"
> "8633","chronic intestinal vascular insufficiency","mondo","0004622"
> "8632","Kaposi's sarcoma","icd10cm","C46"
> "8632","Kaposi's sarcoma","icd10cm","C46.0"
> "8632","Kaposi's sarcoma","icd10cm","C46.1"
> "8632","Kaposi's sarcoma","icd10cm","C46.2"
> "8632","Kaposi's sarcoma","icd10cm","C46.3"
> "8632","Kaposi's sarcoma","icd10cm","C46.4"
> "8632","Kaposi's sarcoma","icd10cm","C46.5"
> "8632","Kaposi's sarcoma","icd10cm","C46.9"
> "8632","Kaposi's sarcoma","icd9cm","176"
> "8632","Kaposi's sarcoma","icd9cm","176.0"
> "8632","Kaposi's sarcoma","icd9cm","176.1"
> "8632","Kaposi's sarcoma","icd9cm","176.2"
> "8632","Kaposi's sarcoma","icd9cm","176.3"
> "8632","Kaposi's sarcoma","icd9cm","176.4"
> "8632","Kaposi's sarcoma","icd9cm","176.5"
> "8632","Kaposi's sarcoma","icd9cm","176.9"
> "8632","Kaposi's sarcoma","mesh","D012514"
> "8632","Kaposi's sarcoma","umls","C0036220"
> "8632","Kaposi's sarcoma","umls","C0153560"
> "8632","Kaposi's sarcoma","umls","C0153561"
> "8632","Kaposi's sarcoma","umls","C0153562"
> "8632","Kaposi's sarcoma","umls","C0153563"
> "8632","Kaposi's sarcoma","umls","C0153564"
> "8632","Kaposi's sarcoma","umls","C0153565"
> "8632","Kaposi's sarcoma","umls","C0346935"
> "8632","Kaposi's sarcoma","umls","C0346936"
> "8632","Kaposi's sarcoma","umls","C1332265"
> "8632","Kaposi's sarcoma","umls","C1332847"
> "8632","Kaposi's sarcoma","umls","C1333453"
> "8632","Kaposi's sarcoma","umls","C1333744"
> "8632","Kaposi's sarcoma","umls","C1333776"
> "8632","Kaposi's sarcoma","umls","C1334318"
> "8632","Kaposi's sarcoma","umls","C1334457"
> "8632","Kaposi's sarcoma","umls","C1335372"
> "8632","Kaposi's sarcoma","umls","C1335509"
> "8632","Kaposi's sarcoma","mondo","0005055"
> "6992","intraocular mixed cell type melanoma","umls","C0279693"
> "6992","intraocular mixed cell type melanoma","mondo","0004062"
> "8630","upper lip cancer","icd10cm","C00.0"
> "8630","upper lip cancer","icd10cm","C00.3"
> "8630","upper lip cancer","icd9cm","140.0"
> "8630","upper lip cancer","icd9cm","140.3"
> "8630","upper lip cancer","umls","C0432579"
> "8630","upper lip cancer","umls","C0474962"
> "8630","upper lip cancer","mondo","0004621"
> "9021","esophageal leukoplakia","icd9cm","530.83"
> "9021","esophageal leukoplakia","umls","C0267095"
> "9021","esophageal leukoplakia","mondo","0004697"
> "2998","testicular cancer","icd10cm","C62"
> "2998","testicular cancer","icd10cm","C62.9"
> "2998","testicular cancer","icd10cm","C62.90"
> "2998","testicular cancer","icd9cm","186"
> "2998","testicular cancer","mesh","D013736"
> "2998","testicular cancer","umls","C0039590"
> "2998","testicular cancer","umls","C0153594"
> "2998","testicular cancer","umls","C1333010"
> "2998","testicular cancer","mondo","0005447"
> "2999","granulosa cell tumor","mesh","D006106"
> "2999","granulosa cell tumor","umls","C0018206"
> "2999","granulosa cell tumor","umls","C0334401"
> "2999","granulosa cell tumor","mondo","0006036"
> "2992","prostate neuroendocrine neoplasm","umls","C1335515"
> "2992","prostate neuroendocrine neoplasm","mondo","0002477"
> "0060491","SPOAN syndrome","icd10cm","G11.4"
> "0060491","SPOAN syndrome","mesh","C563702"
> "0060491","SPOAN syndrome","mondo","0012297"
> "2994","germ cell cancer","mesh","D009373"
> "2994","germ cell cancer","umls","C0205851"
> "2994","germ cell cancer","mondo","0005040"
> "50","thyroid gland disease","icd10cm","E00-E07"
> "50","thyroid gland disease","icd10cm","E07.9"
> "50","thyroid gland disease","icd9cm","240-246.99"
> "50","thyroid gland disease","icd9cm","246.9"
> "50","thyroid gland disease","mesh","D013959"
> "50","thyroid gland disease","umls","C0040128"
> "50","thyroid gland disease","mondo","0003240"
> "2996","mixed germ cell-sex cord neoplasm","umls","C1321220"
> "2996","mixed germ cell-sex cord neoplasm","mondo","0002478"
> "2997","Sertoli-Leydig cell tumor","mesh","D018310"
> "2997","Sertoli-Leydig cell tumor","umls","C0206723"
> "2997","Sertoli-Leydig cell tumor","mondo","0002479"
> "57","aortic valve insufficiency","icd10cm","I06.1"
> "57","aortic valve insufficiency","icd9cm","395.1"
> "57","aortic valve insufficiency","icd9cm","396.3"
> "57","aortic valve insufficiency","mesh","D001022"
> "57","aortic valve insufficiency","umls","C0003504"
> "57","aortic valve insufficiency","umls","C0155568"
> "57","aortic valve insufficiency","umls","C0264774"
> "57","aortic valve insufficiency","mondo","0005648"
> "53","pituitary gland disease","icd9cm","253.1"
> "53","pituitary gland disease","umls","C0029493"
> "53","pituitary gland disease","mondo","0003381"
> "9993","hypoglycemia","icd10cm","E16.2"
> "9993","hypoglycemia","icd9cm","251.2"
> "9993","hypoglycemia","mesh","D007003"
> "9993","hypoglycemia","umls","C0020615"
> "9993","hypoglycemia","mondo","0004946"
> "9997","peripartum cardiomyopathy","icd10cm","O90.3"
> "9997","peripartum cardiomyopathy","icd9cm","674.5"
> "9997","peripartum cardiomyopathy","umls","C0877208"
> "9997","peripartum cardiomyopathy","mondo","0018920"
> "11036","chronic rapidly progressive glomerulonephritis","icd9cm","582.4"
> "11036","chronic rapidly progressive glomerulonephritis","umls","C0341694"
> "11036","chronic rapidly progressive glomerulonephritis","mondo","0001184"
> "11037","dissociative amnesia","icd10cm","F44.0"
> "11037","dissociative amnesia","icd9cm","300.12"
> "11037","dissociative amnesia","mesh","D000647"
> "11037","dissociative amnesia","umls","C0236795"
> "11037","dissociative amnesia","mondo","0001185"
> "11034","contact lens corneal edema","icd9cm","371.24"
> "11034","contact lens corneal edema","umls","C0474442"
> "11034","contact lens corneal edema","mondo","0001183"
> "14515","WAGR syndrome","mesh","D017624"
> "14515","WAGR syndrome","umls","C0206115"
> "14515","WAGR syndrome","mondo","0008681"
> "11032","secondary corneal edema","icd10cm","H18.23"
> "11032","secondary corneal edema","icd9cm","371.22"
> "11032","secondary corneal edema","umls","C0155110"
> "11032","secondary corneal edema","mondo","0001181"
> "11033","idiopathic corneal edema","icd10cm","H18.22"
> "11033","idiopathic corneal edema","icd9cm","371.21"
> "11033","idiopathic corneal edema","umls","C0155109"
> "11033","idiopathic corneal edema","mondo","0001182"
> "11030","corneal edema","icd10cm","H18.20"
> "11030","corneal edema","icd9cm","371.2"
> "11030","corneal edema","icd9cm","371.20"
> "11030","corneal edema","mesh","D015715"
> "11030","corneal edema","umls","C0010037"
> "11030","corneal edema","mondo","0006712"
> "11031","bullous keratopathy","icd10cm","H18.1"
> "11031","bullous keratopathy","icd9cm","371.23"
> "11031","bullous keratopathy","umls","C0155111"
> "11031","bullous keratopathy","mondo","0001180"
> "11038","depersonalization disorder","icd9cm","300.6"
> "11038","depersonalization disorder","mesh","D003861"
> "11038","depersonalization disorder","umls","C0683416"
> "11038","depersonalization disorder","mondo","0001186"
> "429","gynatresia","mesh","D006175"
> "429","gynatresia","umls","C0018414"
> "429","gynatresia","mondo","0002946"
> "1399","primary lacrimal atrophy","icd9cm","375.13"
> "1399","primary lacrimal atrophy","umls","C0155229"
> "1399","primary lacrimal atrophy","mondo","0001851"
> "1398","parasitic infectious disease","icd10cm","H44.12"
> "1398","parasitic infectious disease","icd9cm","360.13"
> "1398","parasitic infectious disease","umls","C0014238"
> "1398","parasitic infectious disease","mondo","0005135"
> "1397","chronic orbital inflammation","icd10cm","H05.1"
> "1397","chronic orbital inflammation","icd9cm","376.1"
> "1397","chronic orbital inflammation","icd9cm","376.10"
> "1397","chronic orbital inflammation","umls","C0155261"
> "1397","chronic orbital inflammation","mondo","0001849"
> "420","hypertrichosis","icd10cm","L68"
> "420","hypertrichosis","icd10cm","L68.3"
> "420","hypertrichosis","icd10cm","L68.9"
> "420","hypertrichosis","mesh","D006983"
> "420","hypertrichosis","umls","C0020555"
> "420","hypertrichosis","mondo","0019280"
> "423","myopathy","icd10cm","G72.9"
> "423","myopathy","icd10cm","M60-M63"
> "423","myopathy","icd10cm","M62.9"
> "423","myopathy","icd9cm","359.9"
> "423","myopathy","mesh","D009135"
> "423","myopathy","umls","C0026848"
> "423","myopathy","mondo","0005336"
> "422","congenital structural myopathy","mesh","D020914"
> "422","congenital structural myopathy","umls","C0752282"
> "422","congenital structural myopathy","mondo","0002921"
> "1393","visual pathway disease","icd10cm","H47.9"
> "1393","visual pathway disease","umls","C0155287"
> "1393","visual pathway disease","mondo","0001834"
> "424","pulmonary immaturity","icd10cm","P28.0"
> "424","pulmonary immaturity","icd9cm","770.4"
> "424","pulmonary immaturity","umls","C0270163"
> "424","pulmonary immaturity","mondo","0002929"
> "1391","Norum disease","icd10cm","E78.6"
> "1391","Norum disease","mesh","D007863"
> "1391","Norum disease","umls","C0023195"
> "1391","Norum disease","mondo","0009515"
> "1390","hypobetalipoproteinemia","mesh","D006995"
> "1390","hypobetalipoproteinemia","umls","C0020597"
> "1390","hypobetalipoproteinemia","mondo","0017774"
> "3450","cutaneous Paget's disease","mesh","D010145"
> "3450","cutaneous Paget's disease","mondo","0002655"
> "3451","skin carcinoma","umls","C0699893"
> "3451","skin carcinoma","mondo","0002656"
> "3456","cervix erosion","mesh","D002579"
> "3456","cervix erosion","umls","C0007869"
> "3456","cervix erosion","mondo","0006696"
> "3457","invasive lobular carcinoma","mesh","D018275"
> "3457","invasive lobular carcinoma","umls","C0206692"
> "3457","invasive lobular carcinoma","mondo","0005051"
> "11353","bladder diverticulum","icd10cm","N32.3"
> "11353","bladder diverticulum","icd9cm","596.3"
> "11353","bladder diverticulum","mesh","C562406"
> "11353","bladder diverticulum","umls","C0156273"
> "11353","bladder diverticulum","mondo","0007197"
> "11355","bladder calculus","icd10cm","N21.0"
> "11355","bladder calculus","mesh","D001744"
> "11355","bladder calculus","umls","C0005683"
> "11355","bladder calculus","mondo","0006678"
> "11354","stone in bladder diverticulum","icd10cm","N21.0"
> "11354","stone in bladder diverticulum","icd9cm","594.0"
> "11354","stone in bladder diverticulum","umls","C0156265"
> "11354","stone in bladder diverticulum","mondo","0001270"
> "1425","pyoureter","umls","C0034223"
> "1425","pyoureter","mondo","0001922"
> "13626","photokeratitis","icd10cm","H16.13"
> "13626","photokeratitis","icd9cm","370.24"
> "13626","photokeratitis","umls","C0155078"
> "13626","photokeratitis","mondo","0001760"
> "6693","testicular monophasic choriocarcinoma","umls","C1515290"
> "6693","testicular monophasic choriocarcinoma","mondo","0003966"
> "6692","Barre-Lieou syndrome","icd10cm","M53.0"
> "6692","Barre-Lieou syndrome","mesh","D055010"
> "6692","Barre-Lieou syndrome","umls","C0376378"
> "6692","Barre-Lieou syndrome","mondo","0005663"
> "6691","Aagenaes syndrome","mesh","C535330"
> "6691","Aagenaes syndrome","umls","C0268314"
> "6691","Aagenaes syndrome","mondo","0008966"
> "6697","asynchronous multifocal osteogenic sarcoma","umls","C1332342"
> "6697","asynchronous multifocal osteogenic sarcoma","mondo","0003968"
> "6696","synchronous multifocal osteogenic sarcoma","umls","C1336544"
> "6696","synchronous multifocal osteogenic sarcoma","mondo","0003967"
> "0070066","autosomal dominant non-syndromic intellectual disability 36","mondo","0014605"
> "0070067","White-Sutton syndrome","mondo","0014606"
> "0070064","autosomal dominant non-syndromic intellectual disability 34","mondo","0014599"
> "2438","dermis tumor","umls","C0346041"
> "2438","dermis tumor","mondo","0002300"
> "0070062","autosomal dominant non-syndromic intellectual disability 32","mondo","0014558"
> "0070063","autosomal dominant non-syndromic intellectual disability 33","mondo","0014580"
> "0070060","autosomal dominant non-syndromic intellectual disability 30","mondo","0014486"
> "0070061","autosomal dominant non-syndromic intellectual disability 31","mondo","0014512"
> "2433","epidermal appendage tumor","umls","C0345988"
> "2433","epidermal appendage tumor","mondo","0002297"
> "2431","glomus tumor","mesh","D005918"
> "2431","glomus tumor","umls","C0017653"
> "2431","glomus tumor","mondo","0018327"
> "2430","skin glomus tumor","umls","C0346083"
> "2430","skin glomus tumor","mondo","0002295"
> "2436","glomangioma","mesh","D005918"
> "2436","glomangioma","umls","C0334421"
> "2436","glomangioma","mondo","0002299"
> "2435","skin glomangioma","umls","C1275226"
> "2435","skin glomangioma","mondo","0002298"
> "0070069","autosomal dominant non-syndromic intellectual disability 39","mondo","0014678"
> "7839","infiltrating nipple syringomatous adenoma","umls","C1518329"
> "7839","infiltrating nipple syringomatous adenoma","mondo","0004376"
> "6345","malignant melanocytic neoplasm of the peripheral nerve sheath","umls","C0474847"
> "6345","malignant melanocytic neoplasm of the peripheral nerve sheath","mondo","0003863"
> "6344","melanocytic psammomatous MPNST","umls","C1513101"
> "6344","melanocytic psammomatous MPNST","mondo","0003862"
> "12117","pulmonary alveolar microlithiasis","icd10cm","J84.02"
> "12117","pulmonary alveolar microlithiasis","icd9cm","516.2"
> "12117","pulmonary alveolar microlithiasis","mesh","C562405"
> "12117","pulmonary alveolar microlithiasis","umls","C0155912"
> "12117","pulmonary alveolar microlithiasis","mondo","0009928"
> "12118","pulmonary hemosiderosis","icd10cm","J84.03"
> "12118","pulmonary hemosiderosis","icd9cm","516.1"
> "12118","pulmonary hemosiderosis","mesh","C536281"
> "12118","pulmonary hemosiderosis","umls","C0020807"
> "12118","pulmonary hemosiderosis","mondo","0008346"
> "12119","hemosiderosis","mesh","D006486"
> "12119","hemosiderosis","umls","C0019114"
> "12119","hemosiderosis","mondo","0001436"
> "9601","ischemic fasciitis","umls","C1304514"
> "9601","ischemic fasciitis","mondo","0004834"
> "9352","type 2 diabetes mellitus","kegg","04930"
> "9352","type 2 diabetes mellitus","icd10cm","E11"
> "9352","type 2 diabetes mellitus","mesh","D003924"
> "9352","type 2 diabetes mellitus","umls","C0011860"
> "9352","type 2 diabetes mellitus","mondo","0005148"
> "9351","diabetes mellitus","icd10cm","E08-E13"
> "9351","diabetes mellitus","icd9cm","250"
> "9351","diabetes mellitus","mesh","D003920"
> "9351","diabetes mellitus","umls","C0011849"
> "9351","diabetes mellitus","mondo","0005015"
> "9602","necrotizing fasciitis","icd10cm","M72.6"
> "9602","necrotizing fasciitis","icd9cm","728.86"
> "9602","necrotizing fasciitis","mesh","D019115"
> "9602","necrotizing fasciitis","umls","C0238124"
> "9602","necrotizing fasciitis","mondo","0004835"
> "9358","fibular collateral ligament bursitis","icd9cm","726.63"
> "9358","fibular collateral ligament bursitis","umls","C0158316"
> "9358","fibular collateral ligament bursitis","mondo","0004764"
> "10174","lacrimal passage granuloma","icd10cm","H04.81"
> "10174","lacrimal passage granuloma","icd9cm","375.81"
> "10174","lacrimal passage granuloma","umls","C0155253"
> "10174","lacrimal passage granuloma","mondo","0000957"
> "10175","optic papillitis","icd10cm","H35.81"
> "10175","optic papillitis","icd10cm","H46.0"
> "10175","optic papillitis","icd10cm","H47.1"
> "10175","optic papillitis","icd10cm","H47.10"
> "10175","optic papillitis","icd10cm","H47.11"
> "10175","optic papillitis","icd9cm","362.83"
> "10175","optic papillitis","icd9cm","377.0"
> "10175","optic papillitis","icd9cm","377.00"
> "10175","optic papillitis","icd9cm","377.01"
> "10175","optic papillitis","icd9cm","377.31"
> "10175","optic papillitis","mesh","D010211"
> "10175","optic papillitis","umls","C0030353"
> "10175","optic papillitis","umls","C0155288"
> "10175","optic papillitis","umls","C0242420"
> "10175","optic papillitis","umls","C0919308"
> "10175","optic papillitis","mondo","0006879"
> "10176","neuroretinitis","icd10cm","H30.9"
> "10176","neuroretinitis","mesh","D012173"
> "10176","neuroretinitis","umls","C0154874"
> "10176","neuroretinitis","mondo","0000958"
> "10177","malignant hypertensive renal disease","umls","C0155593"
> "10177","malignant hypertensive renal disease","mondo","0000959"
> "14512","candidal paronychia","icd10cm","B37.2"
> "14512","candidal paronychia","icd9cm","112.3"
> "14512","candidal paronychia","umls","C0006842"
> "14512","candidal paronychia","mondo","0001984"
> "3783","Coffin-Lowry syndrome","mesh","D038921"
> "3783","Coffin-Lowry syndrome","umls","C0265252"
> "3783","Coffin-Lowry syndrome","mondo","0010561"
> "3781","anovulation","mesh","D000858"
> "3781","anovulation","umls","C0003128"
> "3781","anovulation","mondo","0002775"
> "1803","neuritis","mesh","D009443"
> "1803","neuritis","umls","C0027813"
> "1803","neuritis","mondo","0002122"
> "1802","mononeuritis","icd9cm","355.9"
> "1802","mononeuritis","mesh","D020422"
> "1802","mononeuritis","umls","C0235880"
> "1802","mononeuritis","mondo","0002121"
> "1800","neuroendocrine carcinoma","mesh","D018278"
> "1800","neuroendocrine carcinoma","umls","C0206695"
> "1800","neuroendocrine carcinoma","mondo","0002120"
> "8991","cervix uteri carcinoma in situ","icd10cm","D06"
> "8991","cervix uteri carcinoma in situ","icd10cm","D06.9"
> "8991","cervix uteri carcinoma in situ","icd9cm","233.1"
> "8991","cervix uteri carcinoma in situ","mesh","D018290"
> "8991","cervix uteri carcinoma in situ","umls","C0851140"
> "8991","cervix uteri carcinoma in situ","mondo","0042487"
> "8997","polycythemia vera","icd10cm","D45"
> "8997","polycythemia vera","icd9cm","238.4"
> "8997","polycythemia vera","mesh","D011087"
> "8997","polycythemia vera","umls","C0032463"
> "8997","polycythemia vera","mondo","0009891"
> "4997","Camurati-Engelmann disease","icd10cm","Q78.3"
> "4997","Camurati-Engelmann disease","mesh","C538411"
> "4997","Camurati-Engelmann disease","mesh","D003966"
> "4997","Camurati-Engelmann disease","umls","C0011989"
> "4997","Camurati-Engelmann disease","mondo","0007542"
> "4994","adenomyoma of uterine corpus","umls","C1336903"
> "4994","adenomyoma of uterine corpus","mondo","0003237"
> "4995","cervical adenomyoma","umls","C1516404"
> "4995","cervical adenomyoma","mondo","0003238"
> "4992","optic nerve glioma","mesh","D020339"
> "4992","optic nerve glioma","umls","C0346326"
> "4992","optic nerve glioma","mondo","0003235"
> "4993","atypical polypoid adenomyoma","umls","C1300347"
> "4993","atypical polypoid adenomyoma","mondo","0003236"
> "4990","essential tremor","icd10cm","G25.0"
> "4990","essential tremor","mesh","D020329"
> "4990","essential tremor","umls","C0270736"
> "4990","essential tremor","mondo","0003233"
> "4991","optic nerve astrocytoma","umls","C1335114"
> "4991","optic nerve astrocytoma","umls","C1336971"
> "4991","optic nerve astrocytoma","mondo","0003234"
> "4998","trichorhinophalangeal syndrome type II","mesh","D015826"
> "4998","trichorhinophalangeal syndrome type II","umls","C0023003"
> "4998","trichorhinophalangeal syndrome type II","mondo","0007874"
> "0110197","Charcot-Marie-Tooth disease dominant intermediate B","icd10cm","G60.0"
> "0110197","Charcot-Marie-Tooth disease dominant intermediate B","mondo","0011674"
> "0110196","Charcot-Marie-Tooth disease type 4G","icd10cm","G60.0"
> "0110196","Charcot-Marie-Tooth disease type 4G","mondo","0011534"
> "0110195","Charcot-Marie-Tooth disease type 4E","icd10cm","G60.0"
> "0110195","Charcot-Marie-Tooth disease type 4E","mondo","0011527"
> "0110194","Charcot-Marie-Tooth disease type 4B3","icd10cm","G60.0"
> "0110194","Charcot-Marie-Tooth disease type 4B3","mondo","0014117"
> "0110193","Charcot-Marie-Tooth disease type 4F","icd10cm","G60.0"
> "0110193","Charcot-Marie-Tooth disease type 4F","mondo","0013959"
> "0110192","Charcot-Marie-Tooth disease type 4H","icd10cm","G60.0"
> "0110192","Charcot-Marie-Tooth disease type 4H","mondo","0012250"
> "0110191","Charcot-Marie-Tooth disease type 4B1","icd10cm","G60.0"
> "0110191","Charcot-Marie-Tooth disease type 4B1","mondo","0011066"
> "0110190","Charcot-Marie-Tooth disease type 4B2","icd10cm","G60.0"
> "0110190","Charcot-Marie-Tooth disease type 4B2","mondo","0011475"
> "0002116","pterygium","mesh","D011625"
> "0002116","pterygium","umls","C0033999"
> "0002116","pterygium","mondo","0005085"
> "0110199","Charcot-Marie-Tooth disease dominant intermediate C","icd10cm","G60.0"
> "0110199","Charcot-Marie-Tooth disease dominant intermediate C","mondo","0012012"
> "0110198","Charcot-Marie-Tooth disease recessive intermediate C","icd10cm","G60.0"
> "0110198","Charcot-Marie-Tooth disease recessive intermediate C","mondo","0014154"
> "14075","geniculate ganglionitis","icd10cm","G51.1"
> "14075","geniculate ganglionitis","icd9cm","351.1"
> "14075","geniculate ganglionitis","mesh","D005155"
> "14075","geniculate ganglionitis","umls","C0017407"
> "14075","geniculate ganglionitis","mondo","0001873"
> "3711","bladder adenocarcinoma","umls","C0279682"
> "3711","bladder adenocarcinoma","mondo","0002751"
> "14070","vestibular nystagmus","icd9cm","379.54"
> "14070","vestibular nystagmus","umls","C0155379"
> "14070","vestibular nystagmus","mondo","0001872"
> "3710","bladder colloid adenocarcinoma","umls","C1511193"
> "3710","bladder colloid adenocarcinoma","mondo","0002750"
> "3258","orbit embryonal rhabdomyosarcoma","umls","C1335127"
> "3258","orbit embryonal rhabdomyosarcoma","mondo","0002579"
> "3259","orbit rhabdomyosarcoma","mesh","C537605"
> "3259","orbit rhabdomyosarcoma","umls","C0346347"
> "3259","orbit rhabdomyosarcoma","mondo","0002580"
> "1949","cholecystitis","icd10cm","K81"
> "1949","cholecystitis","icd10cm","K81.9"
> "1949","cholecystitis","icd9cm","575.10"
> "1949","cholecystitis","mesh","D002764"
> "1949","cholecystitis","umls","C0008325"
> "1949","cholecystitis","mondo","0002155"
> "3250","pleomorphic rhabdomyosarcoma","umls","C0334480"
> "3250","pleomorphic rhabdomyosarcoma","mondo","0017386"
> "3251","prostate embryonal rhabdomyosarcoma","umls","C1335508"
> "3251","prostate embryonal rhabdomyosarcoma","mondo","0002574"
> "3252","prostate rhabdomyosarcoma","umls","C1335518"
> "3252","prostate rhabdomyosarcoma","mondo","0006389"
> "3253","embryonal extrahepatic bile duct rhabdomyosarcoma","umls","C1333505"
> "3253","embryonal extrahepatic bile duct rhabdomyosarcoma","mondo","0002576"
> "3254","bile duct rhabdomyosarcoma","umls","C2064434"
> "3254","bile duct rhabdomyosarcoma","mondo","0002577"
> "3255","botryoid rhabdomyosarcoma","umls","C1306573"
> "3255","botryoid rhabdomyosarcoma","mondo","0002578"
> "14140","pulp erosion","icd9cm","521.33"
> "14140","pulp erosion","umls","C1456163"
> "14140","pulp erosion","mondo","0001890"
> "0111572","familial woolly hair syndrome","mesh","C536745"
> "0111572","familial woolly hair syndrome","umls","C0343073"
> "0111573","autosomal dominant woolly hair","umls","C1860238"
> "13241","Behcet's disease","icd10cm","M35.2"
> "13241","Behcet's disease","icd9cm","136.1"
> "13241","Behcet's disease","mesh","D001528"
> "13241","Behcet's disease","umls","C0004943"
> "13241","Behcet's disease","mondo","0007191"
> "13240","tooth resorption","icd10cm","K03.3"
> "13240","tooth resorption","icd9cm","521.4"
> "13240","tooth resorption","mesh","D014091"
> "13240","tooth resorption","umls","C0040451"
> "13240","tooth resorption","mondo","0001670"
> "0111575","dehydrated hereditary stomatocytosis","mesh","C536764"
> "0111575","dehydrated hereditary stomatocytosis","umls","C0272051"
> "13249","pneumatosis cystoides intestinalis","mesh","D011006"
> "13249","pneumatosis cystoides intestinalis","umls","C0032266"
> "13249","pneumatosis cystoides intestinalis","mondo","0006912"
> "13248","mucocele of appendix","umls","C0026684"
> "13248","mucocele of appendix","mondo","0001671"
> "1947","trichomoniasis","icd10cm","A59"
> "1947","trichomoniasis","icd10cm","A59.9"
> "1947","trichomoniasis","icd9cm","131"
> "1947","trichomoniasis","icd9cm","131.9"
> "1947","trichomoniasis","mesh","D014245"
> "1947","trichomoniasis","umls","C0040921"
> "1947","trichomoniasis","mondo","0002154"
> "2859","hemoglobin C disease","icd10cm","D58.2"
> "2859","hemoglobin C disease","mesh","D006445"
> "2859","hemoglobin C disease","umls","C0019021"
> "2859","hemoglobin C disease","mondo","0016242"
> "0110220","Brugada syndrome 3","icd10cm","I49.8"
> "0110220","Brugada syndrome 3","mondo","0012742"
> "0110223","Brugada syndrome 6","icd10cm","I49.8"
> "0110223","Brugada syndrome 6","mondo","0013145"
> "0110222","Brugada syndrome 5","icd10cm","I49.8"
> "0110222","Brugada syndrome 5","mondo","0013015"
> "0110225","Brugada syndrome 8","icd10cm","I49.8"
> "0110225","Brugada syndrome 8","mondo","0013148"
> "0110224","Brugada syndrome 7","icd10cm","I49.8"
> "0110224","Brugada syndrome 7","mondo","0013146"
> "0110227","cataract 32 multiple types","icd10cm","Q12.0"
> "0110227","cataract 32 multiple types","mondo","0007278"
> "0110226","Brugada syndrome 9","icd10cm","I49.8"
> "0110226","Brugada syndrome 9","mondo","0014621"
> "0110229","cataract 6 multiple types","icd10cm","Q12.0"
> "0110229","cataract 6 multiple types","mondo","0007288"
> "0110228","cataract 8 multiple types","icd10cm","Q12.0"
> "0110228","cataract 8 multiple types","mondo","0007280"
> "1358","maxillary sinus neoplasm","mesh","D008444"
> "1358","maxillary sinus neoplasm","umls","C0024958"
> "1358","maxillary sinus neoplasm","mondo","0006850"
> "2855","hyperthyroxinemia","mesh","D006981"
> "2855","hyperthyroxinemia","umls","C0020551"
> "2855","hyperthyroxinemia","mondo","0005333"
> "2856","euthyroid sick syndrome","icd10cm","E07.81"
> "2856","euthyroid sick syndrome","icd9cm","790.94"
> "2856","euthyroid sick syndrome","mesh","D005067"
> "2856","euthyroid sick syndrome","umls","C0015190"
> "2856","euthyroid sick syndrome","mondo","0006755"
> "14219","renal tubular acidosis","icd10cm","N25.89"
> "14219","renal tubular acidosis","mesh","D000141"
> "14219","renal tubular acidosis","umls","C0001126"
> "14219","renal tubular acidosis","mondo","0001909"
> "3332","haemonchiasis","mesh","D006188"
> "3332","haemonchiasis","umls","C0018477"
> "3332","haemonchiasis","mondo","0005778"
> "5463","cochlear disease","mesh","D015834"
> "5463","cochlear disease","umls","C0009197"
> "5463","cochlear disease","mondo","0003452"
> "3330","partial sensory epilepsy","mesh","D020937"
> "3330","partial sensory epilepsy","umls","C0752322"
> "3330","partial sensory epilepsy","mondo","0006892"
> "5465","conjunctival intraepithelial neoplasm","umls","C1333148"
> "5465","conjunctival intraepithelial neoplasm","mondo","0003453"
> "1495","cystic echinococcosis","icd10cm","B67.4"
> "1495","cystic echinococcosis","icd9cm","122.4"
> "1495","cystic echinococcosis","umls","C0152068"
> "1495","cystic echinococcosis","mondo","0018408"
> "5467","conjunctival cancer","icd10cm","C69.0"
> "5467","conjunctival cancer","icd9cm","190.3"
> "5467","conjunctival cancer","mesh","D003230"
> "5467","conjunctival cancer","umls","C0009761"
> "5467","conjunctival cancer","umls","C0153628"
> "5467","conjunctival cancer","mondo","0003454"
> "5468","biliary papillomatosis","umls","C1266038"
> "5468","biliary papillomatosis","mondo","0003455"
> "14213","hypophosphatasia","icd10cm","E83.39"
> "14213","hypophosphatasia","mesh","C562440"
> "14213","hypophosphatasia","mesh","D007014"
> "14213","hypophosphatasia","umls","C0020630"
> "14213","hypophosphatasia","umls","C0220743"
> "14213","hypophosphatasia","mondo","0018570"
> "1395","schistosomiasis","icd9cm","120.8"
> "1395","schistosomiasis","mesh","D012552"
> "1395","schistosomiasis","umls","C0029827"
> "1395","schistosomiasis","mondo","0015254"
> "1394","urinary schistosomiasis","icd9cm","120.0"
> "1394","urinary schistosomiasis","mesh","D012553"
> "1394","urinary schistosomiasis","umls","C0276926"
> "1394","urinary schistosomiasis","mondo","0006001"
> "1392","pseudopapilledema","icd9cm","377.24"
> "1392","pseudopapilledema","mesh","C562401"
> "1392","pseudopapilledema","umls","C0155300"
> "1392","pseudopapilledema","mondo","0008331"
> "5222","acute necrotizing encephalitis","mesh","D004684"
> "5222","acute necrotizing encephalitis","umls","C0338418"
> "5222","acute necrotizing encephalitis","mondo","0003336"
> "5225","von Economo's disease","icd10cm","A85.8"
> "5225","von Economo's disease","umls","C0014040"
> "5225","von Economo's disease","mondo","0019384"
> "0040066","melphalan allergy","umls","C0570673"
> "0080057","autosomal recessive spinocerebellar ataxia 15","mondo","0014311"
> "0110469","autosomal recessive nonsyndromic deafness 14","icd10cm","H90.3"
> "0110469","autosomal recessive nonsyndromic deafness 14","mondo","0011360"
> "525","central nervous system vasculitis","mesh","D020293"
> "525","central nervous system vasculitis","umls","C0751878"
> "525","central nervous system vasculitis","mondo","0003346"
> "526","human immunodeficiency virus infectious disease","icd10cm","B20"
> "526","human immunodeficiency virus infectious disease","icd10cm","B20-B20"
> "526","human immunodeficiency virus infectious disease","icd9cm","042"
> "526","human immunodeficiency virus infectious disease","icd9cm","042-042.99"
> "526","human immunodeficiency virus infectious disease","mesh","D015658"
> "526","human immunodeficiency virus infectious disease","umls","C0019693"
> "526","human immunodeficiency virus infectious disease","mondo","0005109"
> "0110468","autosomal recessive nonsyndromic deafness 13","icd10cm","H90.3"
> "0110468","autosomal recessive nonsyndromic deafness 13","mondo","0011286"
> "520","aortic disease","mesh","D001018"
> "520","aortic disease","umls","C0003493"
> "520","aortic disease","mondo","0005561"
> "528","hydrarthrosis","icd9cm","719.08"
> "528","hydrarthrosis","mesh","D006833"
> "528","hydrarthrosis","umls","C0158157"
> "528","hydrarthrosis","mondo","0003366"
> "529","blepharospasm","icd10cm","G24.5"
> "529","blepharospasm","icd9cm","333.81"
> "529","blepharospasm","mesh","D001764"
> "529","blepharospasm","umls","C0005747"
> "529","blepharospasm","mondo","0011728"
> "11864","peripheral focal chorioretinitis","icd9cm","363.04"
> "11864","peripheral focal chorioretinitis","umls","C0339394"
> "11864","peripheral focal chorioretinitis","mondo","0001393"
> "1234","gender identity disorder","icd10cm","F64.2"
> "1234","gender identity disorder","icd9cm","302.6"
> "1234","gender identity disorder","umls","C0236802"
> "1234","gender identity disorder","mondo","0001500"
> "1235","fetishism","icd10cm","F65.0"
> "1235","fetishism","icd9cm","302.81"
> "1235","fetishism","mesh","D005329"
> "1235","fetishism","umls","C0015957"
> "1235","fetishism","mondo","0001504"
> "1237","corneal degeneration","icd10cm","H18.4"
> "1237","corneal degeneration","icd10cm","H18.40"
> "1237","corneal degeneration","icd9cm","371.4"
> "1237","corneal degeneration","icd9cm","371.40"
> "1237","corneal degeneration","umls","C0155118"
> "1237","corneal degeneration","mondo","0001515"
> "1233","transvestism","icd10cm","F64.1"
> "1233","transvestism","icd10cm","F65.1"
> "1233","transvestism","icd9cm","302.3"
> "1233","transvestism","mesh","D014190"
> "1233","transvestism","umls","C0040774"
> "1233","transvestism","mondo","0001494"
> "0110463","autosomal recessive nonsyndromic deafness 102","icd10cm","H90.3"
> "0110463","autosomal recessive nonsyndromic deafness 102","mondo","0014428"
> "8282","adult epithelioid sarcoma","umls","C0279545"
> "8282","adult epithelioid sarcoma","mondo","0004521"
> "8283","peritonitis","icd9cm","567.8"
> "8283","peritonitis","icd9cm","567.89"
> "8283","peritonitis","mesh","D010538"
> "8283","peritonitis","umls","C0029823"
> "8283","peritonitis","mondo","0004522"
> "0110462","autosomal recessive nonsyndromic deafness 101","icd10cm","H90.3"
> "0110462","autosomal recessive nonsyndromic deafness 101","mondo","0014363"
> "0110461","X-linked dilated cardiomyopathy","icd10cm","I42.0"
> "0110461","X-linked dilated cardiomyopathy","mesh","C580047"
> "0110461","X-linked dilated cardiomyopathy","mondo","0010542"
> "8288","clear cell squamous cell skin carcinoma","umls","C0345978"
> "8288","clear cell squamous cell skin carcinoma","mondo","0004523"
> "0110460","dilated cardiomyopathy 2A","icd10cm","I42.0"
> "0110460","dilated cardiomyopathy 2A","mondo","0012746"
> "0110467","autosomal recessive nonsyndromic deafness 12","icd10cm","H90.3"
> "0110467","autosomal recessive nonsyndromic deafness 12","mondo","0011067"
> "6501","brain stem angioblastoma","umls","C1332611"
> "6501","brain stem angioblastoma","mondo","0003902"
> "6500","cerebellar angioblastoma","umls","C1332900"
> "6500","cerebellar angioblastoma","mondo","0003901"
> "6505","vaginal spindle cell epithelioma","umls","C1511107"
> "6505","vaginal spindle cell epithelioma","mondo","0003903"
> "4677","keratitis","icd10cm","H16"
> "4677","keratitis","icd10cm","H16.9"
> "4677","keratitis","icd9cm","370"
> "4677","keratitis","icd9cm","370.9"
> "4677","keratitis","mesh","D007634"
> "4677","keratitis","umls","C0022568"
> "4677","keratitis","mondo","0003085"
> "0110465","autosomal recessive nonsyndromic deafness 104","icd10cm","H90.3"
> "0110465","autosomal recessive nonsyndromic deafness 104","mondo","0014675"
> "0110464","autosomal recessive nonsyndromic deafness 103","icd10cm","H90.3"
> "0110464","autosomal recessive nonsyndromic deafness 103","mondo","0014469"
> "4675","uremic neuropathy","umls","C0268708"
> "4675","uremic neuropathy","mondo","0003084"
> "4674","androgen insensitivity syndrome","icd10cm","E34.5"
> "4674","androgen insensitivity syndrome","icd10cm","E34.50"
> "4674","androgen insensitivity syndrome","icd10cm","E34.51"
> "4674","androgen insensitivity syndrome","icd9cm","259.5"
> "4674","androgen insensitivity syndrome","icd9cm","259.51"
> "4674","androgen insensitivity syndrome","mesh","D013734"
> "4674","androgen insensitivity syndrome","umls","C0039585"
> "4674","androgen insensitivity syndrome","umls","C0936016"
> "4674","androgen insensitivity syndrome","mondo","0019154"
> "3809","epidural spinal canal meningioma","umls","C1333417"
> "3809","epidural spinal canal meningioma","mondo","0002778"
> "10095","intracranial abscess","icd9cm","324.0"
> "10095","intracranial abscess","umls","C0021874"
> "10095","intracranial abscess","mondo","0000939"
> "3805","porokeratosis","icd10cm","L56.5"
> "3805","porokeratosis","icd9cm","692.75"
> "3805","porokeratosis","mesh","D017499"
> "3805","porokeratosis","umls","C0162839"
> "3805","porokeratosis","umls","C0265970"
> "3805","porokeratosis","mondo","0006602"
> "3803","Crigler-Najjar syndrome","icd10cm","E80.5"
> "3803","Crigler-Najjar syndrome","mesh","D003414"
> "3803","Crigler-Najjar syndrome","umls","C0010324"
> "3803","Crigler-Najjar syndrome","mondo","0009044"
> "8463","corneal ulcer","icd10cm","H16.0"
> "8463","corneal ulcer","icd10cm","H16.00"
> "8463","corneal ulcer","icd9cm","370.0"
> "8463","corneal ulcer","icd9cm","370.00"
> "8463","corneal ulcer","mesh","D003320"
> "8463","corneal ulcer","umls","C0010043"
> "8463","corneal ulcer","mondo","0004577"
> "8461","Aicardi syndrome","mesh","D058540"
> "8461","Aicardi syndrome","umls","C0175713"
> "8461","Aicardi syndrome","mondo","0010568"
> "8466","retinal degeneration","mesh","D012162"
> "8466","retinal degeneration","umls","C0035304"
> "8466","retinal degeneration","mondo","0004580"
> "4671","freemartinism","mesh","D005611"
> "4671","freemartinism","umls","C0016697"
> "4671","freemartinism","mondo","0006762"
> "8464","flat retinoschisis","icd9cm","361.11"
> "8464","flat retinoschisis","umls","C0154817"
> "8464","flat retinoschisis","mondo","0004578"
> "8465","retinoschisis","icd10cm","H33.10"
> "8465","retinoschisis","icd9cm","361.10"
> "8465","retinoschisis","mesh","D041441"
> "8465","retinoschisis","umls","C0152439"
> "8465","retinoschisis","mondo","0004579"
> "8469","influenza","icd10cm","J11.1"
> "8469","influenza","icd9cm","487"
> "8469","influenza","mesh","D007251"
> "8469","influenza","umls","C0021400"
> "8469","influenza","mondo","0005812"
> "7559","asymmetric motor neuropathy","umls","C1332341"
> "7559","asymmetric motor neuropathy","mondo","0004280"
> "7558","glossopharyngeal motor neuropathy","mesh","D020435"
> "7558","glossopharyngeal motor neuropathy","umls","C0751942"
> "7558","glossopharyngeal motor neuropathy","mondo","0004279"
> "0060689","atrichia with papular lesions","icd10cm","L65.8"
> "0060689","atrichia with papular lesions","mondo","0008847"
> "0060688","arteriovenous malformations of the brain","icd10cm","Q28.2"
> "0060688","arteriovenous malformations of the brain","mesh","D002538"
> "0060688","arteriovenous malformations of the brain","umls","C0007772"
> "0060688","arteriovenous malformations of the brain","mondo","0007154"
> "7553","infiltrating bladder urothelial carcinoma sarcomatoid variant","umls","C1512743"
> "7553","infiltrating bladder urothelial carcinoma sarcomatoid variant","mondo","0004278"
> "0060686","autosomal dominant nocturnal frontal lobe epilepsy 5","mondo","0014002"
> "7551","gonorrhea","icd10cm","A54"
> "7551","gonorrhea","icd10cm","A54.9"
> "7551","gonorrhea","icd9cm","098"
> "7551","gonorrhea","mesh","D006069"
> "7551","gonorrhea","umls","C0018081"
> "7551","gonorrhea","mondo","0004277"
> "0060684","autosomal dominant nocturnal frontal lobe epilepsy 3","mondo","0011545"
> "0060683","autosomal dominant nocturnal frontal lobe epilepsy 2","mondo","0011297"
> "0060682","autosomal dominant nocturnal frontal lobe epilepsy 1","mondo","0010899"
> "0060681","autosomal dominant nocturnal frontal lobe epilepsy","mondo","0020300"
> "0060680","pigment dispersion syndrome","mesh","C563184"
> "0060680","pigment dispersion syndrome","mondo","0010896"
> "4175","Rh isoimmunization","mesh","D012203"
> "4175","Rh isoimmunization","umls","C0035404"
> "4175","Rh isoimmunization","mondo","0006953"
> "4176","blood group incompatibility","mesh","D001787"
> "4176","blood group incompatibility","umls","C0005806"
> "4176","blood group incompatibility","mondo","0002901"
> "14498","lipoid proteinosis","mesh","D008065"
> "14498","lipoid proteinosis","umls","C0023795"
> "14498","lipoid proteinosis","mondo","0009530"
> "0050709","early infantile epileptic encephalopathy","mondo","0016021"
> "0050256","angiostrongyliasis","mondo","0019143"
> "0050700","cardiomyopathy","icd10cm","I42"
> "0050700","cardiomyopathy","icd10cm","I42.9"
> "0050700","cardiomyopathy","icd10cm","I51.5"
> "0050700","cardiomyopathy","icd9cm","425"
> "0050700","cardiomyopathy","icd9cm","425.9"
> "0050700","cardiomyopathy","mesh","D009202"
> "0050700","cardiomyopathy","umls","C0033141"
> "0050700","cardiomyopathy","umls","C0036529"
> "0050700","cardiomyopathy","umls","C0878544"
> "0050700","cardiomyopathy","mondo","0004994"
> "0080119","mitochondrial DNA depletion syndrome 1","mesh","C536350"
> "0080119","mitochondrial DNA depletion syndrome 1","mondo","0011283"
> "0080118","mitochondrial complex III deficiency nuclear type 9","mondo","0014496"
> "0080111","mitochondrial complex III deficiency nuclear type 1","mondo","0007415"
> "0080110","multiple pterygium syndrome","mesh","C537377"
> "0080110","multiple pterygium syndrome","mondo","0017415"
> "0080113","mitochondrial complex III deficiency nuclear type 4","mondo","0014065"
> "0080112","mitochondrial complex III deficiency nuclear type 3","mondo","0014064"
> "0080115","mitochondrial complex III deficiency nuclear type 6","mondo","0014194"
> "0080114","mitochondrial complex III deficiency nuclear type 5","mondo","0014066"
> "0080117","mitochondrial complex III deficiency nuclear type 8","mondo","0014364"
> "990","congenital heart block","icd10cm","Q24.6"
> "990","congenital heart block","icd9cm","746.86"
> "990","congenital heart block","mesh","C535758"
> "990","congenital heart block","umls","C0149530"
> "990","congenital heart block","mondo","0009326"
> "0111019","cone-rod dystrophy 12","mondo","0012983"
> "0111018","cone-rod dystrophy 11","mondo","0012483"
> "2228","thrombocytosis","mesh","D013922"
> "2228","thrombocytosis","umls","C0836924"
> "2228","thrombocytosis","mondo","0002249"
> "0060673","Peters anomaly","icd10cm","Q13.4"
> "0060673","Peters anomaly","mesh","C537884"
> "0060673","Peters anomaly","mondo","0011414"
> "0111015","Newfoundland cone-rod dystrophy","mondo","0011839"
> "0111014","cone-rod dystrophy 8","mondo","0011564"
> "0111017","cone-rod dystrophy 10","mondo","0012464"
> "0111016","cone-rod dystrophy 13","mondo","0011987"
> "0111011","cone-rod dystrophy 6","mondo","0011143"
> "0111010","cone-rod dystrophy 5","mondo","0010969"
> "0111013","cone-rod dystrophy 3","mondo","0011395"
> "0111012","cone-rod dystrophy 7","mondo","0011355"
> "5926","extrahepatic bile duct small cell adenocarcinoma","umls","C1335979"
> "5926","extrahepatic bile duct small cell adenocarcinoma","mondo","0003708"
> "5921","adult brainstem mixed glioma","umls","C1377915"
> "5921","adult brainstem mixed glioma","mondo","0003705"
> "5922","adult brainstem astrocytoma","umls","C1332191"
> "5922","adult brainstem astrocytoma","mondo","0003706"
> "5923","distal biliary tract carcinoma","umls","C1333308"
> "5923","distal biliary tract carcinoma","mondo","0003707"
> "7398","cerebral primitive neuroectodermal tumor","mesh","D018242"
> "7398","cerebral primitive neuroectodermal tumor","umls","C0751675"
> "7398","cerebral primitive neuroectodermal tumor","mondo","0004209"
> "4505","pediatric angiosarcoma","umls","C0279988"
> "4505","pediatric angiosarcoma","mondo","0003022"
> "4504","central nervous system angiosarcoma","umls","C1332875"
> "4504","central nervous system angiosarcoma","mondo","0003021"
> "13476","supraglottis cancer","icd10cm","C32.1"
> "13476","supraglottis cancer","icd9cm","161.1"
> "13476","supraglottis cancer","umls","C0153484"
> "13476","supraglottis cancer","mondo","0001724"
> "13477","balanitis xerotica obliterans","icd9cm","607.81"
> "13477","balanitis xerotica obliterans","mesh","D052798"
> "13477","balanitis xerotica obliterans","umls","C0152460"
> "13477","balanitis xerotica obliterans","mondo","0001725"
> "4501","orofaciodigital syndrome","mesh","D009958"
> "4501","orofaciodigital syndrome","umls","C0029294"
> "4501","orofaciodigital syndrome","mondo","0015375"
> "4500","hypokalemia","umls","C1514284"
> "4500","hypokalemia","mondo","0003019"
> "13473","central pterygium","icd9cm","372.43"
> "13473","central pterygium","umls","C0155156"
> "13473","central pterygium","mondo","0001722"
> "0060678","catecholaminergic polymorphic ventricular tachycardia 4","icd10cm","I47.2"
> "0060678","catecholaminergic polymorphic ventricular tachycardia 4","mondo","0013966"
> "0090037","torsion dystonia 13","icd10cm","G24.1"
> "0090037","torsion dystonia 13","mondo","0011886"
> "0090036","myoclonic dystonia 26","mondo","0014620"
> "0090035","myoclonic dystonia 15","mondo","0011844"
> "0090034","myoclonic dystonia 11","icd10cm","G24.1"
> "0090034","myoclonic dystonia 11","mondo","0008044"
> "0090032","Silverman-Handmaker type dyssegmental dysplasia","icd10cm","Q77.7"
> "0090032","Silverman-Handmaker type dyssegmental dysplasia","mondo","0009140"
> "0090031","D-bifunctional protein deficiency","icd10cm","E71.3"
> "0090031","D-bifunctional protein deficiency","mondo","0009855"
> "0090030","corticosteroid-binding globulin deficiency","icd10cm","E27.8"
> "0090030","corticosteroid-binding globulin deficiency","mondo","0012675"
> "2080","vulvar trichoepithelioma","umls","C1520100"
> "2080","vulvar trichoepithelioma","mondo","0002201"
> "0090039","torsion dystonia 6","icd10cm","G24.1"
> "0090039","torsion dystonia 6","mondo","0011264"
> "0090038","torsion dystonia 2","icd10cm","G24.1"
> "0090038","torsion dystonia 2","mondo","0009141"
> "11653","conjunctival deposit","icd10cm","H11.11"
> "11653","conjunctival deposit","icd9cm","372.56"
> "11653","conjunctival deposit","umls","C0162280"
> "11653","conjunctival deposit","mondo","0001331"
> "11656","cicatricial pemphigoid","icd10cm","L12.1"
> "11656","cicatricial pemphigoid","icd9cm","694.6"
> "11656","cicatricial pemphigoid","icd9cm","694.61"
> "11656","cicatricial pemphigoid","mesh","D010390"
> "11656","cicatricial pemphigoid","umls","C0030804"
> "11656","cicatricial pemphigoid","umls","C0157721"
> "11656","cicatricial pemphigoid","mondo","0018746"
> "0110768","hereditary spastic paraplegia 15","icd10cm","G11.4"
> "0110768","hereditary spastic paraplegia 15","mondo","0010044"
> "0110769","hereditary spastic paraplegia 16","icd10cm","G11.4"
> "0110769","hereditary spastic paraplegia 16","mondo","0010287"
> "0110764","hereditary spastic paraplegia 11","icd10cm","G11.4"
> "0110764","hereditary spastic paraplegia 11","mondo","0011445"
> "0110765","hereditary spastic paraplegia 12","icd10cm","G11.4"
> "0110765","hereditary spastic paraplegia 12","mondo","0011489"
> "0110766","hereditary spastic paraplegia 13","icd10cm","G11.4"
> "0110766","hereditary spastic paraplegia 13","mondo","0011532"
> "0110767","hereditary spastic paraplegia 14","icd10cm","G11.4"
> "0110767","hereditary spastic paraplegia 14","mondo","0011522"
> "0110760","type 1 diabetes mellitus 23","icd10cm","E10"
> "0110760","type 1 diabetes mellitus 23","mondo","0012961"
> "0110761","type 1 diabetes mellitus 24","icd10cm","E10"
> "0110761","type 1 diabetes mellitus 24","mondo","0013078"
> "0110763","hereditary spastic paraplegia 10","icd10cm","G11.4"
> "0110763","hereditary spastic paraplegia 10","mondo","0011408"
> "12388","neurohypophyseal diabetes insipidus","mesh","D020790"
> "12388","neurohypophyseal diabetes insipidus","umls","C0687720"
> "12388","neurohypophyseal diabetes insipidus","mondo","0007450"
> "0070239","primary coenzyme Q10 deficiency 2","mondo","0013837"
> "0070238","primary coenzyme Q10 deficiency 1","mondo","0011829"
> "7319","axonal neuropathy","umls","C0270921"
> "7319","axonal neuropathy","mondo","0004183"
> "7315","Jewett-Marshall bladder cancer","umls","C1336362"
> "7315","Jewett-Marshall bladder cancer","mondo","0004182"
> "0070232","benign recurrent intrahepatic cholestasis 2","umls","C2608083"
> "0070232","benign recurrent intrahepatic cholestasis 2","umls","C3489789"
> "0070232","benign recurrent intrahepatic cholestasis 2","mondo","0011559"
> "0070231","benign recurrent intrahepatic cholestasis 1","umls","C1855731"
> "0070231","benign recurrent intrahepatic cholestasis 1","mondo","0009469"
> "0070230","benign recurrent intrahepatic cholestasis","umls","C0149841"
> "0070230","benign recurrent intrahepatic cholestasis","mondo","0019008"
> "0070237","Loeys-Dietz syndrome 3","mondo","0013426"
> "0070236","Loeys-Dietz syndrome 5","mondo","0014262"
> "0070235","Loeys-Dietz syndrome 1","mondo","0012212"
> "7312","breast adenomyoepithelial adenosis","umls","C1511283"
> "7312","breast adenomyoepithelial adenosis","mondo","0004181"
> "0110508","autosomal recessive nonsyndromic deafness 51","icd10cm","H90.3"
> "0110508","autosomal recessive nonsyndromic deafness 51","mondo","0012370"
> "0110509","autosomal recessive nonsyndromic deafness 53","icd10cm","H90.3"
> "0110509","autosomal recessive nonsyndromic deafness 53","mondo","0012333"
> "12307","anterior corneal pigmentation","icd10cm","H18.01"
> "12307","anterior corneal pigmentation","icd9cm","371.11"
> "12307","anterior corneal pigmentation","umls","C0155104"
> "12307","anterior corneal pigmentation","mondo","0001488"
> "12306","vitiligo","icd10cm","L80"
> "12306","vitiligo","icd9cm","709.01"
> "12306","vitiligo","mesh","D014820"
> "12306","vitiligo","umls","C0042900"
> "12306","vitiligo","mondo","0008661"
> "11907","ecthyma","mesh","D004473"
> "11907","ecthyma","umls","C0013568"
> "11907","ecthyma","mondo","0001404"
> "11905","labium majus cancer","icd10cm","C51.0"
> "11905","labium majus cancer","icd9cm","184.1"
> "11905","labium majus cancer","umls","C0496814"
> "11905","labium majus cancer","mondo","0001403"
> "0110500","autosomal recessive nonsyndromic deafness 42","icd10cm","H90.3"
> "0110500","autosomal recessive nonsyndromic deafness 42","mondo","0012326"
> "0110501","autosomal recessive nonsyndromic deafness 44","icd10cm","H90.3"
> "0110501","autosomal recessive nonsyndromic deafness 44","mondo","0012421"
> "0110502","autosomal recessive nonsyndromic deafness 45","icd10cm","H90.3"
> "0110502","autosomal recessive nonsyndromic deafness 45","mondo","0012903"
> "0110503","autosomal recessive nonsyndromic deafness 46","icd10cm","H90.3"
> "0110503","autosomal recessive nonsyndromic deafness 46","mondo","0012327"
> "0110504","autosomal recessive nonsyndromic deafness 47","icd10cm","H90.3"
> "0110504","autosomal recessive nonsyndromic deafness 47","mondo","0012375"
> "0110505","autosomal recessive nonsyndromic deafness 48","icd10cm","H90.3"
> "0110505","autosomal recessive nonsyndromic deafness 48","mondo","0012273"
> "0110506","autosomal recessive nonsyndromic deafness 49","icd10cm","H90.3"
> "0110506","autosomal recessive nonsyndromic deafness 49","mondo","0012420"
> "0110507","autosomal recessive nonsyndromic deafness 5","icd10cm","H90.3"
> "0110507","autosomal recessive nonsyndromic deafness 5","mondo","0000912"
> "12905","sialolithiasis","icd10cm","K11.5"
> "12905","sialolithiasis","icd9cm","527.5"
> "12905","sialolithiasis","mesh","D015494"
> "12905","sialolithiasis","umls","C0036091"
> "12905","sialolithiasis","mondo","0006970"
> "12904","mucocele of salivary gland","icd10cm","K11.6"
> "12904","mucocele of salivary gland","icd9cm","527.6"
> "12904","mucocele of salivary gland","umls","C0026686"
> "12904","mucocele of salivary gland","mondo","0001600"
> "12901","necrotizing sialometaplasia","icd10cm","K11.8"
> "12901","necrotizing sialometaplasia","mesh","D012797"
> "12901","necrotizing sialometaplasia","umls","C0037033"
> "12901","necrotizing sialometaplasia","mondo","0006864"
> "12900","Mikulicz disease","icd10cm","K11.8"
> "12900","Mikulicz disease","mesh","D008882"
> "12900","Mikulicz disease","umls","C0026103"
> "12900","Mikulicz disease","mondo","0019191"
> "7030","bronchial mucus gland adenoma","umls","C1332640"
> "7030","bronchial mucus gland adenoma","mondo","0004079"
> "7031","glottis squamous cell carcinoma","umls","C0280325"
> "7031","glottis squamous cell carcinoma","mondo","0004080"
> "7032","bile duct clear cell adenocarcinoma","umls","C0861855"
> "7032","bile duct clear cell adenocarcinoma","mondo","0004081"
> "7033","anisakiasis","icd10cm","B81.0"
> "7033","anisakiasis","icd9cm","127.1"
> "7033","anisakiasis","mesh","D017129"
> "7033","anisakiasis","umls","C0162576"
> "7033","anisakiasis","mondo","0015200"
> "9011","larynx carcinoma in situ","icd10cm","D02.0"
> "9011","larynx carcinoma in situ","icd9cm","231.0"
> "9011","larynx carcinoma in situ","umls","C0154069"
> "9011","larynx carcinoma in situ","mondo","0004696"
> "10235","Brown's tendon sheath syndrome","icd10cm","H50.61"
> "10235","Brown's tendon sheath syndrome","icd9cm","378.61"
> "10235","Brown's tendon sheath syndrome","mesh","D015835"
> "10235","Brown's tendon sheath syndrome","umls","C0155339"
> "10235","Brown's tendon sheath syndrome","mondo","0000982"
> "7037","childhood immature teratoma of ovary","umls","C1332990"
> "7037","childhood immature teratoma of ovary","mondo","0004082"
> "7039","Borst-Jadassohn intraepidermal carcinoma","umls","C0334260"
> "7039","Borst-Jadassohn intraepidermal carcinoma","mondo","0004083"
> "12382","complex partial epilepsy","mesh","D017029"
> "12382","complex partial epilepsy","umls","C0085417"
> "12382","complex partial epilepsy","mondo","0006710"
> "12732","intermediate uveitis","mesh","D015867"
> "12732","intermediate uveitis","umls","C0042166"
> "12732","intermediate uveitis","mondo","0006806"
> "0060308","autosomal recessive non-syndromic intellectual disability","mondo","0019502"
> "0060309","syndromic X-linked intellectual disability","mondo","0020119"
> "0060302","type II complement component 8 deficiency","icd10cm","D84.1"
> "0060302","type II complement component 8 deficiency","mondo","0013421"
> "0060303","complement component 9 deficiency","icd10cm","D84.1"
> "0060303","complement component 9 deficiency","mondo","0013445"
> "0060300","complement component 7 deficiency","icd10cm","D84.1"
> "0060300","complement component 7 deficiency","mondo","0012412"
> "0060301","type I complement component 8 deficiency","icd10cm","D84.1"
> "0060301","type I complement component 8 deficiency","mondo","0013422"
> "0060306","Meier-Gorlin syndrome","mesh","C538012"
> "0060306","Meier-Gorlin syndrome","umls","C1868684"
> "0060306","Meier-Gorlin syndrome","mondo","0016817"
> "0060307","autosomal dominant non-syndromic intellectual disability","mondo","0015802"
> "0060304","dyschromatosis universalis hereditaria","mesh","C535730"
> "0060304","dyschromatosis universalis hereditaria","umls","C2930995"
> "0060304","dyschromatosis universalis hereditaria","mondo","0000736"
> "0060305","megalocornea","mesh","C562829"
> "0060305","megalocornea","umls","C0344530"
> "0060305","megalocornea","mondo","0009576"
> "7788","adult spinal cord ependymoma","umls","C1332215"
> "7788","adult spinal cord ependymoma","mondo","0004361"
> "7787","breast osteosarcoma","umls","C1335149"
> "7787","breast osteosarcoma","mondo","0004360"
> "0050882","spinocerebellar ataxia type 5","mondo","0010848"
> "0050883","infantile cerebellar-retinal degeneration","mondo","0013802"
> "0050880","Koolen de Vries syndrome","mondo","0012496"
> "0050881","inclusion body myopathy with Paget disease of bone and frontotemporal dementia","mondo","0000507"
> "0050886","Troyer syndrome","icd10cm","G11.4"
> "0050886","Troyer syndrome","mondo","0010156"
> "0050887","Townes-Brocks syndrome","mondo","0007142"
> "0050884","triosephosphate isomerase deficiency","mondo","0014221"
> "0050885","IMAGe syndrome","mondo","0013873"
> "0050889","non-syndromic intellectual disability","mondo","0000509"
> "1005","endometrial disease","umls","C0151622"
> "1005","endometrial disease","mondo","0000931"
> "1003","pelvic inflammatory disease","icd10cm","N70-N77"
> "1003","pelvic inflammatory disease","icd10cm","N73.9"
> "1003","pelvic inflammatory disease","icd9cm","614-616.99"
> "1003","pelvic inflammatory disease","icd9cm","614.9"
> "1003","pelvic inflammatory disease","mesh","D000292"
> "1003","pelvic inflammatory disease","umls","C0242172"
> "1003","pelvic inflammatory disease","mondo","0000922"
> "1002","endometritis","mesh","D004716"
> "1002","endometritis","umls","C0014179"
> "1002","endometritis","mondo","0000918"
> "0110808","hereditary spastic paraplegia 56","icd10cm","G11.4"
> "0110808","hereditary spastic paraplegia 56","mondo","0014015"
> "4347","lymphocele","mesh","D008210"
> "4347","lymphocele","umls","C0024248"
> "4347","lymphocele","mondo","0002968"
> "4346","variegate porphyria","mesh","D046350"
> "4346","variegate porphyria","umls","C0162532"
> "4346","variegate porphyria","mondo","0008297"
> "11014","anorectal stricture","icd10cm","K62.4"
> "11014","anorectal stricture","icd9cm","569.2"
> "11014","anorectal stricture","mesh","D000071056"
> "11014","anorectal stricture","umls","C0156183"
> "11014","anorectal stricture","mondo","0001177"
> "13714","anodontia","icd10cm","K00.0"
> "13714","anodontia","icd9cm","520.0"
> "13714","anodontia","mesh","D000848"
> "13714","anodontia","umls","C0399352"
> "13714","anodontia","mondo","0008797"
> "8616","Peyronie's disease","icd10cm","N48.6"
> "8616","Peyronie's disease","icd9cm","607.85"
> "8616","Peyronie's disease","mesh","D010411"
> "8616","Peyronie's disease","umls","C0030848"
> "8616","Peyronie's disease","mondo","0008231"
> "8619","recurrent hypersomnia","icd10cm","G47.13"
> "8619","recurrent hypersomnia","icd9cm","327.13"
> "8619","recurrent hypersomnia","mesh","D006970"
> "8619","recurrent hypersomnia","umls","C0751226"
> "8619","recurrent hypersomnia","mondo","0004617"
> "8618","oral cavity cancer","icd10cm","C04"
> "8618","oral cavity cancer","icd10cm","C04.0"
> "8618","oral cavity cancer","icd10cm","C04.1"
> "8618","oral cavity cancer","icd10cm","C04.9"
> "8618","oral cavity cancer","icd9cm","144"
> "8618","oral cavity cancer","icd9cm","144.0"
> "8618","oral cavity cancer","icd9cm","144.1"
> "8618","oral cavity cancer","icd9cm","144.9"
> "8618","oral cavity cancer","umls","C0153368"
> "8618","oral cavity cancer","umls","C0153369"
> "8618","oral cavity cancer","umls","C0496758"
> "8618","oral cavity cancer","mondo","0005515"
> "13717","mature cataract","umls","C0152257"
> "13717","mature cataract","mondo","0001782"
> "11330","erysipelas","icd10cm","A46"
> "11330","erysipelas","icd9cm","035"
> "11330","erysipelas","mesh","D004886"
> "11330","erysipelas","umls","C0014733"
> "11330","erysipelas","mondo","0001266"
> "11335","sarcoidosis","icd10cm","D80-D89"
> "11335","sarcoidosis","icd10cm","D86"
> "11335","sarcoidosis","icd10cm","D86.9"
> "11335","sarcoidosis","icd9cm","135"
> "11335","sarcoidosis","mesh","D012507"
> "11335","sarcoidosis","umls","C0036202"
> "11335","sarcoidosis","mondo","0019338"
> "11337","Lemierre's syndrome","icd9cm","040.3"
> "11337","Lemierre's syndrome","mesh","D005674"
> "11337","Lemierre's syndrome","umls","C0027537"
> "11337","Lemierre's syndrome","mondo","0015306"
> "11336","rhinoscleroma","icd9cm","040.1"
> "11336","rhinoscleroma","mesh","D012226"
> "11336","rhinoscleroma","umls","C0035468"
> "11336","rhinoscleroma","mondo","0005945"
> "11339","pneumocystosis","icd10cm","B59"
> "11339","pneumocystosis","icd9cm","136.3"
> "11339","pneumocystosis","mesh","D011020"
> "11339","pneumocystosis","umls","C1535939"
> "11339","pneumocystosis","mondo","0019121"
> "11338","tetanus","icd10cm","A35"
> "11338","tetanus","icd9cm","037"
> "11338","tetanus","mesh","D013742"
> "11338","tetanus","umls","C0039614"
> "11338","tetanus","mondo","0005526"
> "5719","adrenal medulla cancer","icd10cm","C74.1"
> "5719","adrenal medulla cancer","umls","C0344456"
> "5719","adrenal medulla cancer","umls","C0596046"
> "5719","adrenal medulla cancer","mondo","0003606"
> "5718","adrenal neuroblastoma","umls","C0559460"
> "5718","adrenal neuroblastoma","mondo","0006076"
> "5716","hormone producing pituitary cancer","umls","C0278864"
> "5716","hormone producing pituitary cancer","umls","C0851693"
> "5716","hormone producing pituitary cancer","mondo","0003604"
> "5715","functionless pituitary adenoma","umls","C0338078"
> "5715","functionless pituitary adenoma","mondo","0019613"
> "5714","intracranial liposarcoma","umls","C1334242"
> "5714","intracranial liposarcoma","mondo","0003602"
> "5713","mediastinum liposarcoma","umls","C1334663"
> "5713","mediastinum liposarcoma","mondo","0003601"
> "5712","cutaneous liposarcoma","umls","C1333175"
> "5712","cutaneous liposarcoma","mondo","0003600"
> "5711","vulvar liposarcoma","mondo","0003599"
> "11488","idiopathic peripheral autonomic neuropathy","icd10cm","G90.0"
> "11488","idiopathic peripheral autonomic neuropathy","icd10cm","G90.09"
> "11488","idiopathic peripheral autonomic neuropathy","icd9cm","337.0"
> "11488","idiopathic peripheral autonomic neuropathy","umls","C0154690"
> "11488","idiopathic peripheral autonomic neuropathy","mondo","0001295"
> "11486","Horner's syndrome","icd10cm","G90.2"
> "11486","Horner's syndrome","mesh","D006732"
> "11486","Horner's syndrome","umls","C0019937"
> "11486","Horner's syndrome","mondo","0001294"
> "11482","hemopericardium","icd9cm","423.0"
> "11482","hemopericardium","mesh","D010490"
> "11482","hemopericardium","umls","C0019064"
> "11482","hemopericardium","mondo","0005783"
> "11481","constrictive pericarditis","icd9cm","423.2"
> "11481","constrictive pericarditis","mesh","D010494"
> "11481","constrictive pericarditis","umls","C0031048"
> "11481","constrictive pericarditis","mondo","0006711"
> "0110806","hereditary spastic paraplegia 54","icd10cm","G11.4"
> "0110806","hereditary spastic paraplegia 54","mondo","0014018"
> "7246","lymphoepithelioma-like acinar prostate adenocarcinoma","umls","C1515864"
> "7246","lymphoepithelioma-like acinar prostate adenocarcinoma","mondo","0004164"
> "7244","bladder urachal urothelial carcinoma","umls","C1511207"
> "7244","bladder urachal urothelial carcinoma","mondo","0004163"
> "7242","uterine corpus cellular leiomyoma","umls","C1519845"
> "7242","uterine corpus cellular leiomyoma","mondo","0004162"
> "12680","pseudobulbar palsy","icd9cm","335.23"
> "12680","pseudobulbar palsy","mesh","D020828"
> "12680","pseudobulbar palsy","umls","C0033790"
> "12680","pseudobulbar palsy","mondo","0006930"
> "12683","vestibular neuronitis","icd10cm","A88.1"
> "12683","vestibular neuronitis","icd10cm","H81.2"
> "12683","vestibular neuronitis","icd10cm","H81.20"
> "12683","vestibular neuronitis","icd9cm","078.81"
> "12683","vestibular neuronitis","icd9cm","386.12"
> "12683","vestibular neuronitis","mesh","D020338"
> "12683","vestibular neuronitis","umls","C0751908"
> "12683","vestibular neuronitis","mondo","0006008"
> "7241","uterine corpus apoplectic leiomyoma","umls","C1519852"
> "7241","uterine corpus apoplectic leiomyoma","mondo","0004161"
> "12689","acoustic neuroma","mesh","D009464"
> "12689","acoustic neuroma","umls","C0027859"
> "12689","acoustic neuroma","mondo","0001569"
> "3575","cavernous sinus thrombosis","mesh","D020226"
> "3575","cavernous sinus thrombosis","umls","C0238454"
> "3575","cavernous sinus thrombosis","mondo","0002694"
> "10824","malignant hypertension","mesh","D006974"
> "10824","malignant hypertension","umls","C0020540"
> "10824","malignant hypertension","mondo","0006846"
> "10825","essential hypertension","icd10cm","I10"
> "10825","essential hypertension","icd9cm","401"
> "10825","essential hypertension","icd9cm","401.9"
> "10825","essential hypertension","mesh","D000075222"
> "10825","essential hypertension","umls","C0085580"
> "10825","essential hypertension","mondo","0001134"
> "10823","malignant essential hypertension","icd9cm","401.0"
> "10823","malignant essential hypertension","umls","C0024588"
> "10823","malignant essential hypertension","mondo","0001133"
> "0070000","3-methylglutaconic aciduria type 8","mondo","0014988"
> "7817","mixed astrocytoma-ependymoma-oligodendroglioma","umls","C0280792"
> "7817","mixed astrocytoma-ependymoma-oligodendroglioma","mondo","0004366"
> "0070002","3-methylglutaconic aciduria type 9","mondo","0044724"
> "3576","sagittal sinus thrombosis","mesh","D020225"
> "3576","sagittal sinus thrombosis","umls","C0338575"
> "3576","sagittal sinus thrombosis","mondo","0002695"
> "0070005","Seckel syndrome 9","mondo","0014767"
> "0070006","Seckel syndrome 6","mondo","0013871"
> "0070007","Seckel syndrome 1","mondo","0008869"
> "0070008","Seckel syndrome 10","mondo","0014991"
> "0070009","Seckel syndrome 8","mondo","0014350"
> "7818","petroclival meningioma","umls","C1335395"
> "7818","petroclival meningioma","mondo","0004367"
> "7819","sphenoorbital meningioma","umls","C1336040"
> "7819","sphenoorbital meningioma","mondo","0004368"
> "0110109","atrial heart septal defect 4","icd10cm","Q21.1"
> "0110109","atrial heart septal defect 4","mondo","0012654"
> "9378","glaucomatocyclitic crisis","icd9cm","364.22"
> "9378","glaucomatocyclitic crisis","umls","C0152138"
> "9378","glaucomatocyclitic crisis","mondo","0004772"
> "2660","cystic teratoma","umls","C1368903"
> "2660","cystic teratoma","mondo","0002379"
> "2212","coagulation protein disease","mesh","D020147"
> "2212","coagulation protein disease","umls","C0600503"
> "2212","coagulation protein disease","mondo","0002242"
> "9370","exophthalmos","icd10cm","H05.20"
> "9370","exophthalmos","icd9cm","376.30"
> "9370","exophthalmos","mesh","D005094"
> "9370","exophthalmos","umls","C0015300"
> "9370","exophthalmos","mondo","0004770"
> "13381","pernicious anemia","icd10cm","D51.0"
> "13381","pernicious anemia","icd9cm","281.0"
> "13381","pernicious anemia","mesh","D000752"
> "13381","pernicious anemia","umls","C0002892"
> "13381","pernicious anemia","mondo","0008228"
> "9375","Fuchs' heterochromic uveitis","icd10cm","H20.81"
> "9375","Fuchs' heterochromic uveitis","icd9cm","364.21"
> "9375","Fuchs' heterochromic uveitis","umls","C0016782"
> "9375","Fuchs' heterochromic uveitis","mondo","0004771"
> "2211","factor XIII deficiency","mesh","D005177"
> "2211","factor XIII deficiency","umls","C0015530"
> "2211","factor XIII deficiency","mondo","0018029"
> "0050061","erysipeloid","mesh","D004887"
> "0050061","erysipeloid","mondo","0000237"
> "0111024","cone-rod dystrophy 18","mondo","0014153"
> "0111025","cone-rod dystrophy 19","mondo","0014372"
> "0110107","atrial heart septal defect 2","icd10cm","Q21.1"
> "0110107","atrial heart septal defect 2","mondo","0011938"
> "1829","urethral stricture","icd9cm","598.8"
> "1829","urethral stricture","mesh","D014525"
> "1829","urethral stricture","umls","C0029752"
> "1829","urethral stricture","mondo","0002127"
> "0111026","cone-rod dystrophy 20","mondo","0014427"
> "1825","childhood absence epilepsy","mesh","D004832"
> "1825","childhood absence epilepsy","umls","C0014553"
> "1825","childhood absence epilepsy","mondo","0010826"
> "1824","status epilepticus","mesh","D013226"
> "1824","status epilepticus","umls","C0038220"
> "1824","status epilepticus","mondo","0002125"
> "1827","idiopathic generalized epilepsy","mesh","D004829"
> "1827","idiopathic generalized epilepsy","umls","C0014548"
> "1827","idiopathic generalized epilepsy","mondo","0005579"
> "0111027","hemochromatosis type 2A","mondo","0011216"
> "1822","secondary lacrimal atrophy","icd10cm","H04.15"
> "1822","secondary lacrimal atrophy","icd9cm","375.14"
> "1822","secondary lacrimal atrophy","umls","C0339121"
> "1822","secondary lacrimal atrophy","mondo","0002124"
> "2411","granular cell tumor","mesh","D016586"
> "2411","granular cell tumor","umls","C0085167"
> "2411","granular cell tumor","mondo","0006235"
> "2146","ovary sarcoma","umls","C0280746"
> "2146","ovary sarcoma","mondo","0002225"
> "2145","malignant ovarian cyst","umls","C0235770"
> "2145","malignant ovarian cyst","mondo","0002224"
> "2143","ovarian malignant mesothelioma","umls","C1518721"
> "2143","ovarian malignant mesothelioma","mondo","0002223"
> "2142","urethra leiomyoma","umls","C1336888"
> "2142","urethra leiomyoma","mondo","0002222"
> "2140","urethral urothelial papilloma","umls","C1519826"
> "2140","urethral urothelial papilloma","mondo","0002221"
> "4974","actinobacillosis","mesh","D000187"
> "4974","actinobacillosis","umls","C0001247"
> "4974","actinobacillosis","mondo","0005630"
> "4976","elephantiasis","mesh","D004604"
> "4976","elephantiasis","umls","C0013882"
> "4976","elephantiasis","mondo","0005424"
> "4977","lymphedema","mesh","D008209"
> "4977","lymphedema","umls","C0024236"
> "4977","lymphedema","mondo","0019297"
> "4970","prosopagnosia","icd10cm","R48.3"
> "4970","prosopagnosia","mesh","D020238"
> "4970","prosopagnosia","umls","C0234512"
> "4970","prosopagnosia","mondo","0003227"
> "4971","myelofibrosis","icd10cm","D47.4"
> "4971","myelofibrosis","icd10cm","D75.81"
> "4971","myelofibrosis","icd9cm","238.76"
> "4971","myelofibrosis","icd9cm","289.83"
> "4971","myelofibrosis","mesh","D055728"
> "4971","myelofibrosis","umls","C0001815"
> "4971","myelofibrosis","umls","C0026987"
> "4971","myelofibrosis","mondo","0009692"
> "4972","myelodysplastic/myeloproliferative neoplasm","mesh","D054437"
> "4972","myelodysplastic/myeloproliferative neoplasm","umls","C1301355"
> "4972","myelodysplastic/myeloproliferative neoplasm","mondo","0006311"
> "2148","tuberculous oophoritis","icd10cm","A18.17"
> "2148","tuberculous oophoritis","icd9cm","016.6"
> "2148","tuberculous oophoritis","umls","C0152828"
> "2148","tuberculous oophoritis","mondo","0002226"
> "1920","hyperuricemia","mesh","D033461"
> "1920","hyperuricemia","umls","C0740394"
> "1920","hyperuricemia","mondo","0002144"
> "3277","thymus cancer","icd10cm","C37"
> "3277","thymus cancer","icd9cm","164.0"
> "3277","thymus cancer","mesh","D013953"
> "3277","thymus cancer","umls","C0751552"
> "3277","thymus cancer","mondo","0002586"
> "14059","paraurethral gland cancer","icd10cm","C68.1"
> "14059","paraurethral gland cancer","icd9cm","189.4"
> "14059","paraurethral gland cancer","umls","C0153621"
> "14059","paraurethral gland cancer","mondo","0001869"
> "3275","thymoma","mesh","D013945"
> "3275","thymoma","umls","C0040100"
> "3275","thymoma","mondo","0006456"
> "1924","hypogonadism","mesh","D007006"
> "1924","hypogonadism","umls","C0020619"
> "1924","hypogonadism","mondo","0002146"
> "1925","Coffin-Siris syndrome","mesh","C536436"
> "1925","Coffin-Siris syndrome","umls","C0265338"
> "1925","Coffin-Siris syndrome","mondo","0015452"
> "1926","Gaucher's disease","icd10cm","E75.22"
> "1926","Gaucher's disease","mesh","D005776"
> "1926","Gaucher's disease","umls","C0017205"
> "1926","Gaucher's disease","mondo","0018150"
> "1927","sphingolipidosis","icd10cm","E75.3"
> "1927","sphingolipidosis","mesh","D013106"
> "1927","sphingolipidosis","umls","C0037899"
> "1927","sphingolipidosis","mondo","0019255"
> "1928","Williams-Beuren syndrome","mesh","D018980"
> "1928","Williams-Beuren syndrome","umls","C0175702"
> "1928","Williams-Beuren syndrome","mondo","0008678"
> "1929","supravalvular aortic stenosis","icd10cm","Q25.3"
> "1929","supravalvular aortic stenosis","mesh","D021921"
> "1929","supravalvular aortic stenosis","umls","C0003499"
> "1929","supravalvular aortic stenosis","mondo","0008504"
> "3278","encapsulated thymoma","umls","C1333383"
> "3278","encapsulated thymoma","mondo","0002587"
> "3279","spindle cell thymoma","umls","C1266091"
> "3279","spindle cell thymoma","mondo","0002588"
> "13223","uterine fibroid","icd10cm","D25"
> "13223","uterine fibroid","icd10cm","D25.9"
> "13223","uterine fibroid","icd9cm","218"
> "13223","uterine fibroid","icd9cm","218.9"
> "13223","uterine fibroid","mesh","D007889"
> "13223","uterine fibroid","umls","C0042133"
> "13223","uterine fibroid","mondo","0007886"
> "13222","submucous uterine fibroid","icd10cm","D25.0"
> "13222","submucous uterine fibroid","icd9cm","218.0"
> "13222","submucous uterine fibroid","umls","C0153993"
> "13222","submucous uterine fibroid","mondo","0001664"
> "0111590","Cohen syndrome","mesh","C536438"
> "0111590","Cohen syndrome","umls","C0265223"
> "0111591","congenital heart defects, hamartomas of tongue, and polysyndactyly","mesh","C535849"
> "0111591","congenital heart defects, hamartomas of tongue, and polysyndactyly","umls","C2931046"
> "13227","retinal dystrophies primarily involving Bruch's membrane","icd9cm","362.77"
> "13227","retinal dystrophies primarily involving Bruch's membrane","umls","C0154866"
> "13227","retinal dystrophies primarily involving Bruch's membrane","mondo","0001666"
> "13226","oculoglandular tularemia","icd10cm","A21.1"
> "13226","oculoglandular tularemia","icd9cm","021.3"
> "13226","oculoglandular tularemia","umls","C0152944"
> "13226","oculoglandular tularemia","mondo","0001665"
> "0110249","cataract 11 multiple types","icd10cm","Q12.0"
> "0110249","cataract 11 multiple types","mondo","0012527"
> "0090113","RIDDLE syndrome","icd10cm","D82.8"
> "0090113","RIDDLE syndrome","mesh","C567453"
> "0090113","RIDDLE syndrome","mondo","0012764"
> "14233","orbital cyst","icd10cm","H05.81"
> "14233","orbital cyst","icd9cm","376.81"
> "14233","orbital cyst","umls","C0155285"
> "14233","orbital cyst","mondo","0001915"
> "14230","scleromalacia perforans","icd10cm","H15.05"
> "14230","scleromalacia perforans","icd9cm","379.04"
> "14230","scleromalacia perforans","umls","C0155354"
> "14230","scleromalacia perforans","mondo","0001914"
> "0110243","cataract 46 juvenile-onset","icd10cm","Q12.0"
> "0110243","cataract 46 juvenile-onset","mondo","0008925"
> "0110242","cataract 13 with adult i phenotype","icd10cm","Q12.0"
> "0110242","cataract 13 with adult i phenotype","mondo","0007289"
> "0110241","cataract 41","icd10cm","Q12.0"
> "0110241","cataract 41","mondo","0007287"
> "0110240","cataract 20 multiple types","icd10cm","Q12.0"
> "0110240","cataract 20 multiple types","mondo","0007284"
> "0110247","cataract 36","mondo","0013484"
> "0110246","cataract 26 multiple types","icd10cm","Q12.0"
> "0110246","cataract 26 multiple types","mondo","0011591"
> "0110245","cataract 38","icd10cm","Q12.0"
> "0110245","cataract 38","mondo","0013859"
> "0110244","cataract 28","mondo","0012175"
> "3319","lymphangioleiomyomatosis","mesh","D018192"
> "3319","lymphangioleiomyomatosis","umls","C0349649"
> "3319","lymphangioleiomyomatosis","mondo","0006277"
> "3318","epithelioid type angiomyolipoma","umls","C1333426"
> "3318","epithelioid type angiomyolipoma","mondo","0002606"
> "5488","mediastinum synovial sarcoma","umls","C1334681"
> "5488","mediastinum synovial sarcoma","mondo","0003467"
> "5487","spindle cell synovial sarcoma","umls","C0334505"
> "5487","spindle cell synovial sarcoma","mondo","0003466"
> "3310","atopic dermatitis","icd10cm","L20"
> "3310","atopic dermatitis","icd10cm","L20.81"
> "3310","atopic dermatitis","icd10cm","L20.9"
> "3310","atopic dermatitis","mesh","D003876"
> "3310","atopic dermatitis","umls","C0011615"
> "3310","atopic dermatitis","mondo","0004980"
> "5485","synovial sarcoma","mesh","D013584"
> "5485","synovial sarcoma","umls","C0039101"
> "5485","synovial sarcoma","mondo","0010434"
> "3312","bipolar disorder","icd10cm","F31"
> "3312","bipolar disorder","icd10cm","F31.9"
> "3312","bipolar disorder","icd9cm","296.40"
> "3312","bipolar disorder","icd9cm","296.60"
> "3312","bipolar disorder","icd9cm","296.80"
> "3312","bipolar disorder","mesh","D001714"
> "3312","bipolar disorder","umls","C0005586"
> "3312","bipolar disorder","umls","C0005587"
> "3312","bipolar disorder","umls","C0024713"
> "3312","bipolar disorder","umls","C0236780"
> "3312","bipolar disorder","mondo","0004985"
> "3315","lipoma","icd10cm","D17"
> "3315","lipoma","icd10cm","D17.9"
> "3315","lipoma","icd9cm","214"
> "3315","lipoma","icd9cm","214.9"
> "3315","lipoma","mesh","D008067"
> "3315","lipoma","mesh","D018205"
> "3315","lipoma","umls","C0023798"
> "3315","lipoma","umls","C0206631"
> "3315","lipoma","umls","C0346118"
> "3315","lipoma","mondo","0005106"
> "3314","angiomyolipoma","mesh","D018207"
> "3314","angiomyolipoma","umls","C0206633"
> "3314","angiomyolipoma","mondo","0002603"
> "3317","hepatic angiomyolipoma","umls","C1333962"
> "3317","hepatic angiomyolipoma","mondo","0002605"
> "3316","perivascular tumor","umls","C1334611"
> "3316","perivascular tumor","umls","C1335392"
> "3316","perivascular tumor","mondo","0002604"
> "256","hemangioma of spleen","umls","C0685201"
> "256","hemangioma of spleen","mondo","0002343"
> "5325","Roberts syndrome","mesh","C535687"
> "5325","Roberts syndrome","umls","C0392475"
> "5325","Roberts syndrome","mondo","0009997"
> "12537","hypermobility of coccyx","icd9cm","724.71"
> "12537","hypermobility of coccyx","umls","C0158295"
> "12537","hypermobility of coccyx","mondo","0001546"
> "1984","rectal neoplasm","mesh","D012004"
> "1984","rectal neoplasm","umls","C0034885"
> "1984","rectal neoplasm","mondo","0002165"
> "61","mitral valve disease","icd10cm","I05"
> "61","mitral valve disease","icd10cm","I05.1"
> "61","mitral valve disease","icd10cm","I05.9"
> "61","mitral valve disease","icd9cm","394"
> "61","mitral valve disease","icd9cm","394.1"
> "61","mitral valve disease","icd9cm","424.0"
> "61","mitral valve disease","umls","C0026265"
> "61","mitral valve disease","umls","C0155563"
> "61","mitral valve disease","umls","C0264765"
> "61","mitral valve disease","mondo","0003767"
> "62","aortic valve disease","icd9cm","395"
> "62","aortic valve disease","icd9cm","424.1"
> "62","aortic valve disease","umls","C1260873"
> "62","aortic valve disease","mondo","0003803"
> "0070065","autosomal dominant non-syndromic intellectual disability 35","mondo","0014602"
> "65","connective tissue disease","mesh","D003240"
> "65","connective tissue disease","umls","C0009782"
> "65","connective tissue disease","mondo","0003900"
> "0060405","chromosome 17q23.1-q23.2 deletion syndrome","icd10cm","Q93.5"
> "0060405","chromosome 17q23.1-q23.2 deletion syndrome","mondo","0013238"
> "0060407","chromosome 18q deletion syndrome","icd10cm","Q93.5"
> "0060407","chromosome 18q deletion syndrome","mesh","C536580"
> "0060407","chromosome 18q deletion syndrome","mondo","0011147"
> "507","adjustment disorder","icd9cm","309"
> "507","adjustment disorder","icd9cm","309.9"
> "507","adjustment disorder","umls","C0040701"
> "507","adjustment disorder","mondo","0003265"
> "501","central nervous system hemangioma","umls","C1333957"
> "501","central nervous system hemangioma","mondo","0003241"
> "630","genetic disease","mesh","D030342"
> "630","genetic disease","umls","C0019247"
> "630","genetic disease","mondo","0003847"
> "631","fibromyalgia","icd10cm","M79.1"
> "631","fibromyalgia","icd10cm","M79.7"
> "631","fibromyalgia","mesh","D005356"
> "631","fibromyalgia","umls","C0016053"
> "631","fibromyalgia","mondo","0005546"
> "1210","optic neuritis","icd10cm","H46"
> "1210","optic neuritis","icd10cm","H46.9"
> "1210","optic neuritis","icd9cm","377.3"
> "1210","optic neuritis","icd9cm","377.30"
> "1210","optic neuritis","mesh","D009902"
> "1210","optic neuritis","umls","C0029134"
> "1210","optic neuritis","mondo","0005885"
> "633","myositis","icd10cm","G72.49"
> "633","myositis","icd10cm","M60"
> "633","myositis","icd10cm","M60.9"
> "633","myositis","mesh","D009220"
> "633","myositis","umls","C0027121"
> "633","myositis","mondo","0021167"
> "635","acquired immunodeficiency syndrome","icd10cm","B20"
> "635","acquired immunodeficiency syndrome","mesh","D000163"
> "635","acquired immunodeficiency syndrome","umls","C0001175"
> "635","acquired immunodeficiency syndrome","mondo","0012268"
> "636","central pontine myelinolysis","icd10cm","G37.2"
> "636","central pontine myelinolysis","mesh","D017590"
> "636","central pontine myelinolysis","umls","C0206083"
> "636","central pontine myelinolysis","mondo","0006692"
> "639","acute disseminated encephalomyelitis","mesh","D004673"
> "639","acute disseminated encephalomyelitis","umls","C0014059"
> "639","acute disseminated encephalomyelitis","mondo","0019383"
> "1218","echinostomiasis","icd10cm","B66.8"
> "1218","echinostomiasis","mesh","D004451"
> "1218","echinostomiasis","umls","C0013514"
> "1218","echinostomiasis","mondo","0005739"
> "1219","dicrocoeliasis","icd10cm","B66.2"
> "1219","dicrocoeliasis","mesh","D004011"
> "1219","dicrocoeliasis","umls","C0012102"
> "1219","dicrocoeliasis","mondo","0005729"
> "6523","ciliary body mixed cell melanoma","umls","C1333051"
> "6523","ciliary body mixed cell melanoma","mondo","0003911"
> "6522","mixed cell uveal melanoma","umls","C1334782"
> "6522","mixed cell uveal melanoma","mondo","0003910"
> "6525","choroid mixed cell melanoma","umls","C1333025"
> "6525","choroid mixed cell melanoma","mondo","0003913"
> "0070068","autosomal dominant non-syndromic intellectual disability 38","mondo","0014617"
> "0080030","spondyloepimetaphyseal dysplasia, Missouri type","mondo","0011198"
> "1616","benign eccrine breast spiradenoma","umls","C1332492"
> "1616","benign eccrine breast spiradenoma","mondo","0002055"
> "0060408","chromosome 19q13.11 deletion syndrome","mesh","C567810"
> "0060408","chromosome 19q13.11 deletion syndrome","umls","C2751651"
> "0060408","chromosome 19q13.11 deletion syndrome","mondo","0013090"
> "3869","childhood medulloblastoma","mesh","D008527"
> "3869","childhood medulloblastoma","umls","C0278510"
> "3869","childhood medulloblastoma","mondo","0002797"
> "3868","melanotic medulloblastoma","mesh","D008527"
> "3868","melanotic medulloblastoma","umls","C1275668"
> "3868","melanotic medulloblastoma","mondo","0002796"
> "3861","medullomyoblastoma","mesh","D008527"
> "3861","medullomyoblastoma","umls","C0205833"
> "3861","medullomyoblastoma","mondo","0006300"
> "3860","cerebellar vermis medulloblastoma","umls","C1332903"
> "3860","cerebellar vermis medulloblastoma","mondo","0002792"
> "3865","adult central nervous system primitive neuroectodermal neoplasm","umls","C1332196"
> "3865","adult central nervous system primitive neuroectodermal neoplasm","mondo","0002795"
> "3864","adult medulloblastoma","mesh","D008527"
> "3864","adult medulloblastoma","umls","C0278876"
> "3864","adult medulloblastoma","umls","C1332188"
> "3864","adult medulloblastoma","mondo","0002794"
> "8408","Meckel's diverticulitis","umls","C0267497"
> "8408","Meckel's diverticulitis","mondo","0004551"
> "8409","microinvasive cervical squamous cell carcinoma","umls","C1333370"
> "8409","microinvasive cervical squamous cell carcinoma","mondo","0004552"
> "8400","malignant cornea melanoma","umls","C0346367"
> "8400","malignant cornea melanoma","mondo","0004550"
> "7575","pancreatic intraductal papillary-mucinous neoplasm","umls","C1518869"
> "7575","pancreatic intraductal papillary-mucinous neoplasm","mondo","0004286"
> "7574","pancreatic intraductal papillary-colloid carcinoma","umls","C1335304"
> "7574","pancreatic intraductal papillary-colloid carcinoma","mondo","0004285"
> "7577","pancreatic foamy gland adenocarcinoma","umls","C1335303"
> "7577","pancreatic foamy gland adenocarcinoma","mondo","0004287"
> "7578","breast scirrhous carcinoma","umls","C0346151"
> "7578","breast scirrhous carcinoma","mondo","0004288"
> "9810","polyarteritis nodosa","icd10cm","M30.0"
> "9810","polyarteritis nodosa","icd9cm","446.0"
> "9810","polyarteritis nodosa","mesh","D010488"
> "9810","polyarteritis nodosa","umls","C0031036"
> "9810","polyarteritis nodosa","mondo","0019170"
> "9811","partial circumpapillary choroid dystrophy","icd9cm","363.51"
> "9811","partial circumpapillary choroid dystrophy","umls","C0154895"
> "9811","partial circumpapillary choroid dystrophy","mondo","0004888"
> "4152","chondroid chordoma","umls","C1266173"
> "4152","chondroid chordoma","mondo","0006145"
> "4153","spinal chordoma","mondo","0002894"
> "4151","skull base chordoma","umls","C1335975"
> "4151","skull base chordoma","mondo","0002892"
> "4156","primary syphilis","icd9cm","091"
> "4156","primary syphilis","umls","C0153139"
> "4156","primary syphilis","mondo","0002896"
> "4157","secondary syphilis","icd9cm","091.9"
> "4157","secondary syphilis","mesh","C536773"
> "4157","secondary syphilis","umls","C0149985"
> "4157","secondary syphilis","mondo","0002897"
> "4154","dentinogenesis imperfecta","icd10cm","K00.5"
> "4154","dentinogenesis imperfecta","mesh","D003811"
> "4154","dentinogenesis imperfecta","umls","C0011436"
> "4154","dentinogenesis imperfecta","mondo","0018849"
> "4159","skin cancer","mesh","D012878"
> "4159","skin cancer","umls","C0007114"
> "4159","skin cancer","mondo","0002898"
> "13461","urethral intrinsic sphincter deficiency","icd10cm","N36.42"
> "13461","urethral intrinsic sphincter deficiency","icd9cm","599.82"
> "13461","urethral intrinsic sphincter deficiency","umls","C0375381"
> "13461","urethral intrinsic sphincter deficiency","mondo","0001721"
> "8337","appendicitis","icd10cm","K37"
> "8337","appendicitis","icd9cm","540-543.99"
> "8337","appendicitis","icd9cm","541"
> "8337","appendicitis","mesh","D001064"
> "8337","appendicitis","umls","C0003615"
> "8337","appendicitis","mondo","0005649"
> "0080173","bladder exstrophy-epispadias-cloacal exstrophy complex","mondo","0017919"
> "0080172","thiopurine S-methyltransferase deficiency","mondo","0012503"
> "0080171","esophageal atresia/tracheoesophageal fistula","mondo","0008586"
> "0080170","normophosphatemic familial tumoral calcinosis","mondo","0012502"
> "0080177","hepatic veno-occlusive disease","icd10cm","K76.5"
> "0080177","hepatic veno-occlusive disease","mesh","D006504"
> "0080177","hepatic veno-occlusive disease","mondo","0019514"
> "0080176","meningococcal meningitis","icd10cm","A39.0"
> "0080176","meningococcal meningitis","icd9cm","036.0"
> "0080176","meningococcal meningitis","mesh","D008585"
> "0080176","meningococcal meningitis","mondo","0018059"
> "0080175","cloacal exstrophy","mondo","0009774"
> "0080174","bladder exstrophy","icd10cm","Q64.10"
> "0080174","bladder exstrophy","icd9cm","753.5"
> "0080174","bladder exstrophy","mesh","D001746"
> "0080174","bladder exstrophy","mondo","0010805"
> "0080179","haemophilus meningitis","icd10cm","G00.0"
> "0080179","haemophilus meningitis","icd9cm","320.0"
> "0080179","haemophilus meningitis","mesh","D008583"
> "0080179","haemophilus meningitis","mondo","0000889"
> "0080178","mucositis","mesh","D052016"
> "0080178","mucositis","mondo","0000888"
> "8747","subacute myeloid leukemia","umls","C0153889"
> "8747","subacute myeloid leukemia","mondo","0004653"
> "5900","meningeal melanocytoma","umls","C1266113"
> "5900","meningeal melanocytoma","mondo","0016746"
> "5907","penis non-invasive verrucous carcinoma","umls","C1334984"
> "5907","penis non-invasive verrucous carcinoma","mondo","0003697"
> "5908","penis verrucous carcinoma","umls","C1336955"
> "5908","penis verrucous carcinoma","mondo","0003698"
> "3488","cellulitis","icd10cm","L03.90"
> "3488","cellulitis","mesh","D002481"
> "3488","cellulitis","umls","C0007642"
> "3488","cellulitis","umls","C0007646"
> "3488","cellulitis","mondo","0005230"
> "3480","uveal disease","mesh","D014603"
> "3480","uveal disease","umls","C0042161"
> "3480","uveal disease","mondo","0002661"
> "3482","plague","icd10cm","A20"
> "3482","plague","icd10cm","A20.9"
> "3482","plague","icd9cm","020"
> "3482","plague","icd9cm","020.9"
> "3482","plague","mesh","D010930"
> "3482","plague","umls","C0032064"
> "3482","plague","mondo","0019095"
> "3486","necrobiosis lipoidica","mesh","D009335"
> "3486","necrobiosis lipoidica","umls","C0027538"
> "3486","necrobiosis lipoidica","mondo","0006583"
> "4562","subacute bacterial endocarditis","mesh","D004698"
> "4562","subacute bacterial endocarditis","umls","C0014122"
> "4562","subacute bacterial endocarditis","mondo","0006981"
> "4561","granulomatous endometritis","umls","C1333876"
> "4561","granulomatous endometritis","mondo","0003052"
> "4560","non specific chronic endometritis","umls","C1335061"
> "4560","non specific chronic endometritis","mondo","0003051"
> "8741","seborrheic dermatitis","icd10cm","L21"
> "8741","seborrheic dermatitis","icd10cm","L21.9"
> "8741","seborrheic dermatitis","icd9cm","690.1"
> "8741","seborrheic dermatitis","icd9cm","690.10"
> "8741","seborrheic dermatitis","icd9cm","706.3"
> "8741","seborrheic dermatitis","mesh","D012628"
> "8741","seborrheic dermatitis","umls","C0036508"
> "8741","seborrheic dermatitis","mondo","0006608"
> "13419","neurogenic bowel","icd9cm","564.81"
> "13419","neurogenic bowel","mesh","D055496"
> "13419","neurogenic bowel","umls","C0695242"
> "13419","neurogenic bowel","mondo","0006868"
> "0090011","immunodeficiency-centromeric instability-facial anomalies syndrome 4","icd10cm","D84.8"
> "0090011","immunodeficiency-centromeric instability-facial anomalies syndrome 4","mondo","0014829"
> "0090010","immunodeficiency-centromeric instability-facial anomalies syndrome 3","icd10cm","D84.8"
> "0090010","immunodeficiency-centromeric instability-facial anomalies syndrome 3","mondo","0014828"
> "0090013","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive","icd10cm","D81.1"
> "0090013","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive","mondo","0011086"
> "0090012","severe combined immunodeficiency with sensitivity to ionizing radiation","icd10cm","D81.1"
> "0090012","severe combined immunodeficiency with sensitivity to ionizing radiation","mondo","0011225"
> "0090015","Cenani-Lenz syndactyly syndrome","icd10cm","Q78.4"
> "0090015","Cenani-Lenz syndactyly syndrome","mondo","0008931"
> "0090014","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive","icd10cm","D81.2"
> "0090014","severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive","mondo","0012163"
> "0090017","epidermolysis bullosa simplex with muscular dystrophy","icd10cm","Q81.0"
> "0090017","epidermolysis bullosa simplex with muscular dystrophy","mondo","0009181"
> "0090016","chromosome 5q deletion syndrome","icd10cm","D46.7"
> "0090016","chromosome 5q deletion syndrome","mondo","0007925"
> "0090019","sitosterolemia","mesh","C537345"
> "0090019","sitosterolemia","umls","C0342907"
> "0090019","sitosterolemia","mondo","0008863"
> "0090018","autosomal dominant familial periodic fever","icd10cm","E85.0"
> "0090018","autosomal dominant familial periodic fever","mondo","0007727"
> "0080039","axial osteomalacia","mondo","0007181"
> "9600","plantar fasciitis","icd10cm","M72.2"
> "9600","plantar fasciitis","mesh","D036981"
> "9600","plantar fasciitis","umls","C0149756"
> "9600","plantar fasciitis","mondo","0004833"
> "9603","intravascular fasciitis","umls","C0432529"
> "9603","intravascular fasciitis","mondo","0004836"
> "0110746","type 1 diabetes mellitus 7","icd10cm","E10"
> "0110746","type 1 diabetes mellitus 7","mondo","0010864"
> "0110747","type 1 diabetes mellitus 8","icd10cm","E10"
> "0110747","type 1 diabetes mellitus 8","mondo","0010950"
> "0110744","type 1 diabetes mellitus 5","icd10cm","E10"
> "0110744","type 1 diabetes mellitus 5","mondo","0010863"
> "0110745","type 1 diabetes mellitus 6","icd10cm","E10"
> "0110745","type 1 diabetes mellitus 6","mondo","0011167"
> "0110742","type 1 diabetes mellitus 3","icd10cm","E10"
> "0110742","type 1 diabetes mellitus 3","mondo","0010861"
> "0110743","type 1 diabetes mellitus 4","icd10cm","E10"
> "0110743","type 1 diabetes mellitus 4","mondo","0010862"
> "0110740","neurodegeneration with brain iron accumulation 6","icd10cm","G23.0"
> "0110740","neurodegeneration with brain iron accumulation 6","mondo","0014290"
> "0110741","type 1 diabetes mellitus 2","icd10cm","E10"
> "0110741","type 1 diabetes mellitus 2","mondo","0007454"
> "0110748","obsolete type 1 diabetes mellitus 9","icd10cm","E10"
> "0110749","type 1 diabetes mellitus 10","icd10cm","E10"
> "0110749","type 1 diabetes mellitus 10","mondo","0011168"
> "6065","urinary tract non-invasive transitional cell neoplasm","umls","C1518361"
> "6065","urinary tract non-invasive transitional cell neoplasm","mondo","0003755"
> "6067","ovarian mucinous neoplasm","umls","C1335168"
> "6067","ovarian mucinous neoplasm","umls","C1518233"
> "6067","ovarian mucinous neoplasm","mondo","0003756"
> "0050185","erythema multiforme","mesh","D004892"
> "0050185","erythema multiforme","mondo","0006545"
> "12098","trigeminal neuralgia","icd10cm","G50.0"
> "12098","trigeminal neuralgia","icd9cm","350.1"
> "12098","trigeminal neuralgia","mesh","D014277"
> "12098","trigeminal neuralgia","umls","C0040997"
> "12098","trigeminal neuralgia","mondo","0008599"
> "2600","laryngeal carcinoma","umls","C0595989"
> "2600","laryngeal carcinoma","mondo","0002358"
> "2601","juxtacortical chondroma","umls","C0334548"
> "2601","juxtacortical chondroma","mondo","0002359"
> "2602","chondroma","mesh","D002812"
> "2602","chondroma","umls","C0936248"
> "2602","chondroma","mondo","0002360"
> "2609","adenomyoma","mesh","D018194"
> "2609","adenomyoma","umls","C0206622"
> "2609","adenomyoma","mondo","0005635"
> "0070215","familial hyperinsulinemic hypoglycemia 4","mondo","0012382"
> "0070214","familial hyperinsulinemic hypoglycemia 7","umls","C1864902"
> "0070214","familial hyperinsulinemic hypoglycemia 7","mondo","0012396"
> "0070217","familial hyperinsulinemic hypoglycemia 6","mondo","0011717"
> "10780","primary polycythemia","icd10cm","D75.0"
> "10780","primary polycythemia","icd9cm","289.6"
> "10780","primary polycythemia","mesh","C536842"
> "10780","primary polycythemia","umls","C0152264"
> "10780","primary polycythemia","mondo","0001115"
> "0070211","hereditary lymphedema IB","mondo","0012765"
> "0070210","hereditary lymphedema IA","mondo","0007919"
> "0070213","hereditary lymphedema II","umls","C0238261"
> "0070213","hereditary lymphedema II","umls","C1704424"
> "0070213","hereditary lymphedema II","umls","C1704425"
> "0070213","hereditary lymphedema II","mondo","0007920"
> "0070212","hereditary lymphedema I","umls","C1704423"
> "10035","asymptomatic neurosyphilis","icd10cm","A52.2"
> "10035","asymptomatic neurosyphilis","icd9cm","094.3"
> "10035","asymptomatic neurosyphilis","mesh","D009494"
> "10035","asymptomatic neurosyphilis","umls","C0153167"
> "10035","asymptomatic neurosyphilis","mondo","0000927"
> "10034","eye accommodation disease","icd10cm","H52.5"
> "10034","eye accommodation disease","icd9cm","367.5"
> "10034","eye accommodation disease","umls","C0152198"
> "10034","eye accommodation disease","mondo","0000926"
> "0070219","familial hyperinsulinemic hypoglycemia 1","mondo","0009734"
> "0070218","familial hyperinsulinemic hypoglycemia 2","mondo","0011153"
> "10033","cycloplegia","icd10cm","H52.52"
> "10033","cycloplegia","icd9cm","367.51"
> "10033","cycloplegia","umls","C0235238"
> "10033","cycloplegia","mondo","0005555"
> "10032","hyperlucent lung","mesh","D019568"
> "10032","hyperlucent lung","umls","C0524799"
> "10032","hyperlucent lung","mondo","0000925"
> "0110522","autosomal recessive nonsyndromic deafness 71","icd10cm","H90.3"
> "0110522","autosomal recessive nonsyndromic deafness 71","mondo","0013010"
> "0110523","autosomal recessive nonsyndromic deafness 74","icd10cm","H90.3"
> "0110523","autosomal recessive nonsyndromic deafness 74","mondo","0013386"
> "7379","adrenal medulla carcinoma","umls","C1334717"
> "7379","adrenal medulla carcinoma","mondo","0004202"
> "7378","pituitary hypoplasia","umls","C0948740"
> "7378","pituitary hypoplasia","mondo","0004201"
> "0110526","autosomal recessive nonsyndromic deafness 79","icd10cm","H90.3"
> "0110526","autosomal recessive nonsyndromic deafness 79","mondo","0013215"
> "0110527","autosomal recessive nonsyndromic deafness 8","icd10cm","H90.3"
> "0110527","autosomal recessive nonsyndromic deafness 8","mondo","0010987"
> "0110524","autosomal recessive nonsyndromic deafness 76","icd10cm","H90.3"
> "0110524","autosomal recessive nonsyndromic deafness 76","mondo","0014237"
> "0110525","autosomal recessive nonsyndromic deafness 77","icd10cm","H90.3"
> "0110525","autosomal recessive nonsyndromic deafness 77","mondo","0013119"
> "7371","superficial urinary bladder cancer","umls","C1336527"
> "7371","superficial urinary bladder cancer","mondo","0004200"
> "0110529","autosomal recessive nonsyndromic deafness 84A","icd10cm","H90.3"
> "0110529","autosomal recessive nonsyndromic deafness 84A","mondo","0013249"
> "12323","cough variant asthma","icd10cm","J45.991"
> "12323","cough variant asthma","icd9cm","493.82"
> "12323","cough variant asthma","umls","C0694548"
> "12323","cough variant asthma","mondo","0001491"
> "12326","chronic pulmonary heart disease","icd9cm","416.8"
> "12326","chronic pulmonary heart disease","umls","C0155673"
> "12326","chronic pulmonary heart disease","mondo","0001493"
> "12325","kyphoscoliotic heart disease","icd10cm","I27.1"
> "12325","kyphoscoliotic heart disease","icd9cm","416.1"
> "12325","kyphoscoliotic heart disease","umls","C0152102"
> "12325","kyphoscoliotic heart disease","mondo","0001492"
> "11920","tracheal cancer","icd10cm","C33"
> "11920","tracheal cancer","icd9cm","162.0"
> "11920","tracheal cancer","umls","C0153489"
> "11920","tracheal cancer","mondo","0001407"
> "12328","marasmus","icd10cm","E41"
> "12328","marasmus","icd9cm","261"
> "12328","marasmus","mesh","D011502"
> "12328","marasmus","umls","C0086588"
> "12328","marasmus","mondo","0006848"
> "9036","parotid gland cancer","icd10cm","C07"
> "9036","parotid gland cancer","icd9cm","142.0"
> "9036","parotid gland cancer","mesh","D010307"
> "9036","parotid gland cancer","umls","C0747273"
> "9036","parotid gland cancer","mondo","0004700"
> "7016","tendon sheath lipoma","umls","C1336703"
> "7016","tendon sheath lipoma","mondo","0004076"
> "7017","lumbosacral lipoma","umls","C1334438"
> "7017","lumbosacral lipoma","mondo","0004077"
> "7014","infiltrating lipoma","umls","C0334473"
> "7014","infiltrating lipoma","mondo","0004075"
> "5453","pulmonary venoocclusive disease","mesh","D011668"
> "5453","pulmonary venoocclusive disease","umls","C0034091"
> "5453","pulmonary venoocclusive disease","mondo","0009937"
> "13775","plantar wart","icd10cm","B07.0"
> "13775","plantar wart","icd9cm","078.12"
> "13775","plantar wart","umls","C0042548"
> "13775","plantar wart","mondo","0001795"
> "752","peptic ulcer perforation","mesh","D010439"
> "752","peptic ulcer perforation","umls","C0030925"
> "752","peptic ulcer perforation","mondo","0004260"
> "750","peptic ulcer disease","icd10cm","K27"
> "750","peptic ulcer disease","icd9cm","533"
> "750","peptic ulcer disease","mesh","D010437"
> "750","peptic ulcer disease","umls","C0030920"
> "750","peptic ulcer disease","mondo","0004247"
> "754","bladder tuberculosis","icd10cm","A18.12"
> "754","bladder tuberculosis","icd9cm","016.1"
> "754","bladder tuberculosis","icd9cm","016.10"
> "754","bladder tuberculosis","umls","C0152793"
> "754","bladder tuberculosis","mondo","0004272"
> "758","situs inversus","icd10cm","Q89.3"
> "758","situs inversus","icd9cm","759.3"
> "758","situs inversus","mesh","D012857"
> "758","situs inversus","umls","C0037221"
> "758","situs inversus","mondo","0010029"
> "0060180","colitis","icd10cm","K52.9"
> "0060180","colitis","mesh","D003092"
> "0060180","colitis","umls","C0009319"
> "0060180","colitis","mondo","0005292"
> "0060181","ischemic colitis","icd10cm","K55.9"
> "0060181","ischemic colitis","mesh","D017091"
> "0060181","ischemic colitis","umls","C0162529"
> "0060181","ischemic colitis","mondo","0000701"
> "0060182","microscopic colitis","icd10cm","K52.83"
> "0060182","microscopic colitis","mesh","D046728"
> "0060182","microscopic colitis","umls","C0400821"
> "0060182","microscopic colitis","mondo","0000702"
> "0060183","collagenous colitis","icd10cm","K52.831"
> "0060183","collagenous colitis","mesh","D046729"
> "0060183","collagenous colitis","umls","C0238067"
> "0060183","collagenous colitis","mondo","0000703"
> "0060184","lymphocytic colitis","icd10cm","K52.832"
> "0060184","lymphocytic colitis","mesh","D046730"
> "0060184","lymphocytic colitis","umls","C0400822"
> "0060184","lymphocytic colitis","mondo","0000704"
> "2959","hyperimmunoglobulin syndrome","umls","C1334069"
> "2959","hyperimmunoglobulin syndrome","mondo","0002468"
> "0060186","chemical colitis","icd10cm","K52"
> "0060186","chemical colitis","icd9cm","558"
> "0060186","chemical colitis","icd9cm","558.9"
> "0060186","chemical colitis","umls","C0029512"
> "0060186","chemical colitis","mondo","0000706"
> "0060187","diversion colitis","icd10cm","K52"
> "0060187","diversion colitis","icd9cm","558"
> "0060187","diversion colitis","icd9cm","558.9"
> "0060187","diversion colitis","umls","C0029512"
> "0060187","diversion colitis","mondo","0000707"
> "0060188","jejunoileitis","icd10cm","K50.0"
> "0060188","jejunoileitis","mondo","0000708"
> "0060189","ileitis","icd10cm","K52.9"
> "0060189","ileitis","mesh","D007079"
> "0060189","ileitis","umls","C0020877"
> "0060189","ileitis","mondo","0000709"
> "2957","pulmonary tuberculosis","icd10cm","A15"
> "2957","pulmonary tuberculosis","icd10cm","A15.0"
> "2957","pulmonary tuberculosis","icd9cm","011"
> "2957","pulmonary tuberculosis","icd9cm","011.9"
> "2957","pulmonary tuberculosis","icd9cm","011.90"
> "2957","pulmonary tuberculosis","mesh","D014397"
> "2957","pulmonary tuberculosis","umls","C0041327"
> "2957","pulmonary tuberculosis","mondo","0006052"
> "2951","motion sickness","icd10cm","T75.3"
> "2951","motion sickness","icd9cm","994.6"
> "2951","motion sickness","mesh","D009041"
> "2951","motion sickness","umls","C0026603"
> "2951","motion sickness","mondo","0008015"
> "2952","inner ear disease","icd10cm","H80-H83"
> "2952","inner ear disease","icd10cm","H83.9"
> "2952","inner ear disease","icd10cm","H83.90"
> "2952","inner ear disease","mesh","D007759"
> "2952","inner ear disease","umls","C0022890"
> "2952","inner ear disease","umls","C0494559"
> "2952","inner ear disease","mondo","0002467"
> "5344","testicular yolk sac tumor","umls","C0279708"
> "5344","testicular yolk sac tumor","mondo","0003402"
> "5345","testicular non-seminomatous germ cell cancer","umls","C1334625"
> "5345","testicular non-seminomatous germ cell cancer","mondo","0003403"
> "5340","anterograde amnesia","icd10cm","R41.1"
> "5340","anterograde amnesia","mesh","D020324"
> "5340","anterograde amnesia","umls","C0233795"
> "5340","anterograde amnesia","mondo","0003398"
> "5341","pineal region yolk sac tumor","umls","C1335420"
> "5341","pineal region yolk sac tumor","mondo","0003399"
> "5342","childhood endodermal sinus tumor","umls","C1333016"
> "5342","childhood endodermal sinus tumor","mondo","0003400"
> "5343","central nervous system endodermal sinus tumor","umls","C1337040"
> "5343","central nervous system endodermal sinus tumor","umls","C1377613"
> "5343","central nervous system endodermal sinus tumor","mondo","0003401"
> "0050865","tongue squamous cell carcinoma","umls","C0349566"
> "0050865","tongue squamous cell carcinoma","mondo","0000500"
> "0050866","oral squamous cell carcinoma","mondo","0004958"
> "5348","adult endodermal sinus tumor","umls","C1332221"
> "5348","adult endodermal sinus tumor","mondo","0003404"
> "5349","central nervous system adult germ cell tumor","umls","C0280796"
> "5349","central nervous system adult germ cell tumor","mondo","0003405"
> "4364","malignant breast melanoma","umls","C0346787"
> "4364","malignant breast melanoma","mondo","0002975"
> "4367","apparent mineralocorticoid excess syndrome","mesh","D043204"
> "4367","apparent mineralocorticoid excess syndrome","umls","C0342488"
> "4367","apparent mineralocorticoid excess syndrome","mondo","0006657"
> "4360","epithelioid cell melanoma","umls","C0334443"
> "4360","epithelioid cell melanoma","mondo","0002973"
> "4362","cervical cancer","icd10cm","C53"
> "4362","cervical cancer","icd10cm","C53.9"
> "4362","cervical cancer","icd9cm","180"
> "4362","cervical cancer","icd9cm","180.9"
> "4362","cervical cancer","mesh","D002583"
> "4362","cervical cancer","umls","C0007847"
> "4362","cervical cancer","umls","C0007873"
> "4362","cervical cancer","mondo","0002974"
> "11079","leech infestation","icd10cm","B88.3"
> "11079","leech infestation","icd9cm","134.2"
> "11079","leech infestation","umls","C0019575"
> "11079","leech infestation","mondo","0001191"
> "3108","ascaridiasis","mesh","D001198"
> "3108","ascaridiasis","umls","C0003952"
> "3108","ascaridiasis","mondo","0005655"
> "3109","idiopathic CD4-positive T-lymphocytopenia","mesh","D018344"
> "3109","idiopathic CD4-positive T-lymphocytopenia","umls","C0206744"
> "3109","idiopathic CD4-positive T-lymphocytopenia","mondo","0005807"
> "14550","root resorption","mesh","D012391"
> "14550","root resorption","umls","C0035851"
> "14550","root resorption","mondo","0001997"
> "3107","toxascariasis","mesh","D017227"
> "3107","toxascariasis","umls","C0040522"
> "3107","toxascariasis","mondo","0005987"
> "11077","brucellosis","icd10cm","A23"
> "11077","brucellosis","icd10cm","A23.9"
> "11077","brucellosis","icd9cm","023"
> "11077","brucellosis","icd9cm","023.9"
> "11077","brucellosis","mesh","D002006"
> "11077","brucellosis","umls","C0006309"
> "11077","brucellosis","mondo","0005683"
> "3103","thoracic outlet syndrome","icd10cm","G54.0"
> "3103","thoracic outlet syndrome","mesh","D013901"
> "3103","thoracic outlet syndrome","umls","C0039984"
> "3103","thoracic outlet syndrome","mondo","0005979"
> "8672","viral exanthem","icd9cm","057.8"
> "8672","viral exanthem","umls","C0029841"
> "8672","viral exanthem","mondo","0006619"
> "8670","eating disorder","icd10cm","F50"
> "8670","eating disorder","icd10cm","F50.9"
> "8670","eating disorder","icd9cm","307.50"
> "8670","eating disorder","mesh","D001068"
> "8670","eating disorder","umls","C0013473"
> "8670","eating disorder","mondo","0005451"
> "8677","perinatal necrotizing enterocolitis","icd10cm","K55.3"
> "8677","perinatal necrotizing enterocolitis","icd10cm","K55.30"
> "8677","perinatal necrotizing enterocolitis","mesh","D020345"
> "8677","perinatal necrotizing enterocolitis","umls","C0520459"
> "8677","perinatal necrotizing enterocolitis","mondo","0004639"
> "4090","agnosia","icd10cm","R48.1"
> "4090","agnosia","icd10cm","R48.2"
> "4090","agnosia","mesh","D000377"
> "4090","agnosia","mesh","D001072"
> "4090","agnosia","umls","C0001816"
> "4090","agnosia","umls","C0003635"
> "4090","agnosia","mondo","0005638"
> "0060720","autosomal recessive congenital ichthyosis 11","icd10cm","Q80.8"
> "0060720","autosomal recessive congenital ichthyosis 11","mondo","0011218"
> "13787","localized anterior staphyloma","icd10cm","H15.82"
> "13787","localized anterior staphyloma","icd9cm","379.14"
> "13787","localized anterior staphyloma","umls","C0155362"
> "13787","localized anterior staphyloma","mondo","0001799"
> "13788","equatorial staphyloma","icd10cm","H15.81"
> "13788","equatorial staphyloma","icd9cm","379.13"
> "13788","equatorial staphyloma","umls","C0155361"
> "13788","equatorial staphyloma","mondo","0001800"
> "13789","staphyloma posticum","icd10cm","H15.83"
> "13789","staphyloma posticum","icd9cm","379.12"
> "13789","staphyloma posticum","umls","C0155360"
> "13789","staphyloma posticum","mondo","0001801"
> "0060728","NGLY1-deficiency","icd10cm","E77.8"
> "0060728","NGLY1-deficiency","mondo","0014109"
> "13756","epiphora due to insufficient drainage","icd10cm","H04.22"
> "13756","epiphora due to insufficient drainage","icd9cm","375.22"
> "13756","epiphora due to insufficient drainage","umls","C0155234"
> "13756","epiphora due to insufficient drainage","mondo","0001792"
> "5731","chronic salpingitis","icd10cm","N70.11"
> "5731","chronic salpingitis","umls","C0269041"
> "5731","chronic salpingitis","mondo","0003617"
> "5730","salpingitis isthmica nodosa","umls","C0269043"
> "5730","salpingitis isthmica nodosa","mondo","0003616"
> "5733","salpingitis","icd10cm","N70.91"
> "5733","salpingitis","mesh","D012488"
> "5733","salpingitis","umls","C0036130"
> "5733","salpingitis","mondo","0003619"
> "5732","pyosalpinx","icd10cm","N70"
> "5732","pyosalpinx","umls","C0034220"
> "5732","pyosalpinx","mondo","0003618"
> "11316","histoplasmosis retinitis","icd9cm","115.92"
> "11316","histoplasmosis retinitis","umls","C0153278"
> "11316","histoplasmosis retinitis","mondo","0001263"
> "11315","African histoplasmosis","icd9cm","115.10"
> "11315","African histoplasmosis","umls","C0153270"
> "11315","African histoplasmosis","mondo","0001262"
> "11312","Mobitz type II atrioventricular block","icd9cm","426.12"
> "11312","Mobitz type II atrioventricular block","umls","C0155700"
> "11312","Mobitz type II atrioventricular block","mondo","0001261"
> "8097","bladder hepatoid adenocarcinoma","umls","C1511189"
> "8097","bladder hepatoid adenocarcinoma","mondo","0004459"
> "8096","bladder mixed adenocarcinoma","umls","C1511192"
> "8096","bladder mixed adenocarcinoma","mondo","0004458"
> "12527","common peroneal nerve lesion","icd10cm","G57.3"
> "12527","common peroneal nerve lesion","icd10cm","G57.30"
> "12527","common peroneal nerve lesion","icd9cm","355.3"
> "12527","common peroneal nerve lesion","umls","C0270909"
> "12527","common peroneal nerve lesion","mondo","0001542"
> "12526","tarsal tunnel syndrome","icd10cm","G57.5"
> "12526","tarsal tunnel syndrome","icd10cm","G57.50"
> "12526","tarsal tunnel syndrome","icd9cm","355.5"
> "12526","tarsal tunnel syndrome","mesh","D013641"
> "12526","tarsal tunnel syndrome","umls","C0039319"
> "12526","tarsal tunnel syndrome","mondo","0006994"
> "8093","maxillary sinus Schneiderian papilloma","umls","C1334646"
> "8093","maxillary sinus Schneiderian papilloma","mondo","0004457"
> "12522","bagassosis","icd10cm","J67.1"
> "12522","bagassosis","icd9cm","495.1"
> "12522","bagassosis","mesh","D011009"
> "12522","bagassosis","umls","C0004681"
> "12522","bagassosis","mondo","0001540"
> "12529","tibial nerve palsy","umls","C0154751"
> "12529","tibial nerve palsy","mondo","0001544"
> "12528","lesion of sciatic nerve","icd10cm","G57.0"
> "12528","lesion of sciatic nerve","icd10cm","G57.00"
> "12528","lesion of sciatic nerve","icd9cm","355.0"
> "12528","lesion of sciatic nerve","mesh","D020426"
> "12528","lesion of sciatic nerve","umls","C0154748"
> "12528","lesion of sciatic nerve","mondo","0001543"
> "6659","cervical large cell neuroendocrine carcinoma","umls","C1516417"
> "6659","cervical large cell neuroendocrine carcinoma","mondo","0006138"
> "6658","pulmonary large cell neuroendocrine carcinoma","umls","C1265996"
> "6658","pulmonary large cell neuroendocrine carcinoma","umls","C1334363"
> "6658","pulmonary large cell neuroendocrine carcinoma","mondo","0003960"
> "6657","breast large cell neuroendocrine carcinoma","umls","C1511316"
> "6657","breast large cell neuroendocrine carcinoma","mondo","0003959"
> "12667","binocular vision disease","icd10cm","H53.30"
> "12667","binocular vision disease","icd9cm","368.30"
> "12667","binocular vision disease","umls","C0005461"
> "12667","binocular vision disease","mondo","0001564"
> "6654","childhood central nervous system immature teratoma","umls","C1332954"
> "6654","childhood central nervous system immature teratoma","mondo","0003958"
> "12662","paracoccidioidomycosis","icd10cm","B41"
> "12662","paracoccidioidomycosis","icd10cm","B41.9"
> "12662","paracoccidioidomycosis","icd9cm","116.1"
> "12662","paracoccidioidomycosis","mesh","D010229"
> "12662","paracoccidioidomycosis","umls","C0030409"
> "12662","paracoccidioidomycosis","mondo","0005894"
> "6652","diffuse idiopathic skeletal hyperostosis","icd10cm","M48.1"
> "6652","diffuse idiopathic skeletal hyperostosis","icd9cm","721.6"
> "6652","diffuse idiopathic skeletal hyperostosis","mesh","D004057"
> "6652","diffuse idiopathic skeletal hyperostosis","umls","C0020498"
> "6652","diffuse idiopathic skeletal hyperostosis","mondo","0007127"
> "12661","tooth ankylosis","icd10cm","K03.5"
> "12661","tooth ankylosis","icd9cm","521.6"
> "12661","tooth ankylosis","mesh","D020254"
> "12661","tooth ankylosis","umls","C0155930"
> "12661","tooth ankylosis","mondo","0008007"
> "10808","gastric ulcer","icd10cm","K25"
> "10808","gastric ulcer","icd9cm","531"
> "10808","gastric ulcer","mesh","D013276"
> "10808","gastric ulcer","umls","C0038358"
> "10808","gastric ulcer","mondo","0001126"
> "10802","acute gonococcal epididymo-orchitis","icd9cm","098.13"
> "10802","acute gonococcal epididymo-orchitis","umls","C0153193"
> "10802","acute gonococcal epididymo-orchitis","mondo","0001125"
> "0070028","APP-related cerebral amyloid angiopathy","mondo","0011583"
> "0070029","ITM2B-related cerebral amyloid angiopathy 1","mondo","0008306"
> "0070022","autosomal recessive dyskeratosis congenita 5","mondo","0014076"
> "0070023","autosomal dominant dyskeratosis congenita 6","mondo","0014690"
> "0070026","Revesz syndrome","mondo","0009990"
> "0070027","CST3-related cerebral amyloid angiopathy","mondo","0007098"
> "0070024","autosomal recessive dyskeratosis congenita 6","mondo","0014600"
> "0070025","X-linked dyskeratosis congenita","mondo","0010584"
> "6386","childhood brainstem astrocytoma","umls","C1332950"
> "6386","childhood brainstem astrocytoma","mondo","0003870"
> "6381","anterior foramen magnum meningioma","umls","C1332302"
> "6381","anterior foramen magnum meningioma","mondo","0003868"
> "11148","hypersecretion glaucoma","icd10cm","H40.82"
> "11148","hypersecretion glaucoma","icd9cm","365.81"
> "11148","hypersecretion glaucoma","umls","C0154968"
> "11148","hypersecretion glaucoma","mondo","0001205"
> "6383","childhood brain stem glioma","umls","C0278600"
> "6383","childhood brain stem glioma","mondo","0003869"
> "11149","aqueous misdirection","icd10cm","H40.83"
> "11149","aqueous misdirection","icd9cm","365.83"
> "11149","aqueous misdirection","umls","C1135189"
> "11149","aqueous misdirection","mondo","0001206"
> "3660","wheat allergy","mesh","D021182"
> "3660","wheat allergy","umls","C0949570"
> "3660","wheat allergy","mondo","0007021"
> "2383","neonatal jaundice","icd10cm","P59.9"
> "2383","neonatal jaundice","mesh","D007567"
> "2383","neonatal jaundice","umls","C0022353"
> "2383","neonatal jaundice","mondo","0006584"
> "2382","kernicterus","icd10cm","P57"
> "2382","kernicterus","icd10cm","P57.9"
> "2382","kernicterus","mesh","D007647"
> "2382","kernicterus","umls","C0022610"
> "2382","kernicterus","mondo","0006819"
> "2384","Wernicke encephalopathy","icd10cm","E51.2"
> "2384","Wernicke encephalopathy","mesh","D014899"
> "2384","Wernicke encephalopathy","umls","C0043121"
> "2384","Wernicke encephalopathy","mondo","0007020"
> "2388","renal artery disease","icd9cm","593.81"
> "2388","renal artery disease","umls","C0268790"
> "2388","renal artery disease","mondo","0002286"
> "0050451","Brugada syndrome","icd10cm","I49.8"
> "0050451","Brugada syndrome","mesh","D053840"
> "0050451","Brugada syndrome","umls","C1142166"
> "0050451","Brugada syndrome","umls","C1721096"
> "0050451","Brugada syndrome","mondo","0015263"
> "1849","cannabis dependence","icd10cm","F12.2"
> "1849","cannabis dependence","icd9cm","304.3"
> "1849","cannabis dependence","mesh","D002189"
> "1849","cannabis dependence","umls","C0006870"
> "1849","cannabis dependence","mondo","0005689"
> "0070249","autosomal dominant Emery-Dreifuss muscular dystrophy 4","mondo","0013071"
> "0070283","primary autosomal recessive microcephaly 13","mondo","0014473"
> "1844","mononeuritis of upper limb","icd9cm","354.9"
> "1844","mononeuritis of upper limb","umls","C0154746"
> "1844","mononeuritis of upper limb","mondo","0002130"
> "1942","intermittent squint","icd10cm","H50.3"
> "1942","intermittent squint","icd10cm","H50.30"
> "1942","intermittent squint","icd9cm","378.2"
> "1942","intermittent squint","icd9cm","378.20"
> "1942","intermittent squint","umls","C0152210"
> "1942","intermittent squint","mondo","0002152"
> "4959","epidermolysis bullosa dystrophica","icd10cm","Q81.2"
> "4959","epidermolysis bullosa dystrophica","mesh","D016108"
> "4959","epidermolysis bullosa dystrophica","umls","C0079294"
> "4959","epidermolysis bullosa dystrophica","mondo","0006543"
> "1943","telogen effluvium","icd10cm","L65.0"
> "1943","telogen effluvium","icd9cm","704.02"
> "1943","telogen effluvium","umls","C0263518"
> "1943","telogen effluvium","mondo","0002153"
> "4952","postpoliomyelitis syndrome","icd10cm","G14"
> "4952","postpoliomyelitis syndrome","mesh","D016262"
> "4952","postpoliomyelitis syndrome","umls","C0080040"
> "4952","postpoliomyelitis syndrome","mondo","0017416"
> "4953","poliomyelitis","icd10cm","A80"
> "4953","poliomyelitis","icd10cm","A80.9"
> "4953","poliomyelitis","icd9cm","045"
> "4953","poliomyelitis","icd9cm","045.9"
> "4953","poliomyelitis","mesh","D011051"
> "4953","poliomyelitis","umls","C0032371"
> "4953","poliomyelitis","mondo","0017373"
> "4957","meninges hemangiopericytoma","umls","C0349622"
> "4957","meninges hemangiopericytoma","mondo","0003223"
> "2163","nasal cavity disease","umls","C0339820"
> "2163","nasal cavity disease","mondo","0002232"
> "4955","central nervous system melanocytic neoplasm","umls","C0349623"
> "4955","central nervous system melanocytic neoplasm","umls","C1332887"
> "4955","central nervous system melanocytic neoplasm","mondo","0003222"
> "14033","malignant visceral pleura tumor","umls","C0153496"
> "14033","malignant visceral pleura tumor","mondo","0001862"
> "9286","priapism","icd10cm","N48.3"
> "9286","priapism","icd10cm","N48.30"
> "9286","priapism","icd9cm","607.3"
> "9286","priapism","mesh","D011317"
> "9286","priapism","umls","C0033117"
> "9286","priapism","mondo","0004745"
> "2129","atypical teratoid rhabdoid tumor","umls","C1266184"
> "2129","atypical teratoid rhabdoid tumor","mondo","0020560"
> "14037","aorta atresia","icd9cm","747.22"
> "14037","aorta atresia","umls","C0345010"
> "14037","aorta atresia","mondo","0001863"
> "14039","POEMS syndrome","mesh","D016878"
> "14039","POEMS syndrome","umls","C0085404"
> "14039","POEMS syndrome","mondo","0017364"
> "9281","phenylketonuria","icd9cm","270.1"
> "9281","phenylketonuria","mesh","D010661"
> "9281","phenylketonuria","mesh","D017042"
> "9281","phenylketonuria","umls","C0031485"
> "9281","phenylketonuria","umls","C0085547"
> "9281","phenylketonuria","mondo","0009861"
> "0070243","primary coenzyme Q10 deficiency 6","mondo","0013836"
> "3298","vaccinia","mesh","D014615"
> "3298","vaccinia","umls","C0042214"
> "3298","vaccinia","mondo","0002595"
> "0070240","primary coenzyme Q10 deficiency 3","mondo","0013838"
> "5139","cellular leiomyoma","umls","C0334477"
> "5139","cellular leiomyoma","mondo","0003296"
> "5138","leiomyomatosis","mesh","D018231"
> "5138","leiomyomatosis","umls","C0206654"
> "5138","leiomyomatosis","mondo","0003295"
> "5137","pericardium leiomyoma","umls","C1335380"
> "5137","pericardium leiomyoma","mondo","0003294"
> "5136","lung leiomyoma","umls","C1334447"
> "5136","lung leiomyoma","mondo","0003293"
> "5134","anus leiomyoma","umls","C1332266"
> "5134","anus leiomyoma","mondo","0003292"
> "5132","leiomyoma cutis","umls","C0346064"
> "5132","leiomyoma cutis","mondo","0003291"
> "3292","monkeypox","icd10cm","B04"
> "3292","monkeypox","icd9cm","059.01"
> "3292","monkeypox","mesh","D045908"
> "3292","monkeypox","umls","C0276180"
> "3292","monkeypox","mondo","0002594"
> "1901","vagina sarcoma","umls","C0238519"
> "1901","vagina sarcoma","mondo","0002140"
> "13207","proliferative diabetic retinopathy","icd9cm","362.02"
> "13207","proliferative diabetic retinopathy","umls","C0154830"
> "13207","proliferative diabetic retinopathy","mondo","0001660"
> "13206","nodular prostate","icd10cm","N40"
> "13206","nodular prostate","icd9cm","600.1"
> "13206","nodular prostate","umls","C0748012"
> "13206","nodular prostate","mondo","0021259"
> "13200","substernal goiter","mesh","D006045"
> "13200","substernal goiter","umls","C0018024"
> "13200","substernal goiter","mondo","0006986"
> "0111570","snowflake vitreoretinal degeneration","mesh","C536677"
> "0111570","snowflake vitreoretinal degeneration","umls","C1860405"
> "13209","right bundle branch block","icd9cm","426.51"
> "13209","right bundle branch block","umls","C0155704"
> "13209","right bundle branch block","mondo","0001662"
> "13208","background diabetic retinopathy","icd9cm","362.01"
> "13208","background diabetic retinopathy","icd9cm","362.03"
> "13208","background diabetic retinopathy","umls","C0004606"
> "13208","background diabetic retinopathy","mondo","0001661"
> "0111571","Weyers acrofacial dysostosis","mesh","C536695"
> "0111571","Weyers acrofacial dysostosis","umls","C0457013"
> "14789","spondyloepiphyseal dysplasia congenita","mondo","0008471"
> "14784","olivopontocerebellar atrophy","mesh","D009849"
> "14784","olivopontocerebellar atrophy","umls","C0028968"
> "14784","olivopontocerebellar atrophy","mondo","0002017"
> "14780","KBG syndrome","mesh","C537015"
> "14780","KBG syndrome","umls","C0220687"
> "14780","KBG syndrome","mondo","0007846"
> "0111578","Gillespie syndrome","mesh","C536370"
> "0111578","Gillespie syndrome","umls","C0431401"
> "12546","atrophic nonflaccid tympanic membrane","icd10cm","H73.82"
> "12546","atrophic nonflaccid tympanic membrane","icd9cm","384.82"
> "12546","atrophic nonflaccid tympanic membrane","umls","C0155471"
> "12546","atrophic nonflaccid tympanic membrane","mondo","0001547"
> "1733","cryptosporidiosis","icd10cm","A07.2"
> "1733","cryptosporidiosis","icd9cm","007.4"
> "1733","cryptosporidiosis","mesh","D003457"
> "1733","cryptosporidiosis","umls","C0010418"
> "1733","cryptosporidiosis","mondo","0015474"
> "0110221","Brugada syndrome 4","icd10cm","I49.8"
> "0110221","Brugada syndrome 4","mondo","0012743"
> "2575","barbiturate dependence","icd9cm","304.11"
> "2575","barbiturate dependence","umls","C0154482"
> "2575","barbiturate dependence","mondo","0002347"
> "2570","malignant histiocytic disease","mesh","D015620"
> "2570","malignant histiocytic disease","umls","C0019613"
> "2570","malignant histiocytic disease","mondo","0002346"
> "6898","ovarian seromucinous carcinoma","umls","C0279392"
> "6898","ovarian seromucinous carcinoma","mondo","0004031"
> "2571","Langerhans-cell histiocytosis","icd10cm","C96.0"
> "2571","Langerhans-cell histiocytosis","icd10cm","C96.5"
> "2571","Langerhans-cell histiocytosis","icd10cm","C96.6"
> "2571","Langerhans-cell histiocytosis","icd9cm","202.5"
> "2571","Langerhans-cell histiocytosis","mesh","C538636"
> "2571","Langerhans-cell histiocytosis","mesh","D006646"
> "2571","Langerhans-cell histiocytosis","umls","C0019621"
> "2571","Langerhans-cell histiocytosis","umls","C0023381"
> "2571","Langerhans-cell histiocytosis","mondo","0018310"
> "0110265","cataract 31 multiple types","icd10cm","Q12.0"
> "0110265","cataract 31 multiple types","mondo","0011547"
> "0110264","cataract 33","icd10cm","Q12.0"
> "0110264","cataract 33","mondo","0012665"
> "0110267","cataract 44","icd10cm","Q12.0"
> "0110267","cataract 44","mondo","0014673"
> "0110266","cataract 9 multiple types","icd10cm","Q12.0"
> "0110266","cataract 9 multiple types","mondo","0011413"
> "0110261","cataract 35","icd10cm","Q12.0"
> "0110261","cataract 35","mondo","0012260"
> "0110260","cataract 7","icd10cm","Q12.0"
> "0110260","cataract 7","mondo","0007279"
> "0110263","cataract 19 multiple types","icd10cm","Q12.0"
> "0110263","cataract 19 multiple types","mondo","0014111"
> "0110262","cataract 45","icd10cm","Q12.0"
> "0110262","cataract 45","mondo","0014799"
> "0110269","cataract 3 multiple types","icd10cm","Q12.0"
> "0110269","cataract 3 multiple types","mondo","0011104"
> "0110268","cataract 22 multiple types","icd10cm","Q12.0"
> "0110268","cataract 22 multiple types","mondo","0012336"
> "1278","tolosa-hunt syndrome","mesh","D020333"
> "1278","tolosa-hunt syndrome","umls","C0040381"
> "1278","tolosa-hunt syndrome","mondo","0018983"
> "1279","ocular motility disease","icd9cm","378.9"
> "1279","ocular motility disease","mesh","D015835"
> "1279","ocular motility disease","umls","C0028850"
> "1279","ocular motility disease","mondo","0001584"
> "612","primary immunodeficiency disease","kegg","05340"
> "612","primary immunodeficiency disease","icd10cm","D84.9"
> "612","primary immunodeficiency disease","icd9cm","279.3"
> "612","primary immunodeficiency disease","mesh","D007153"
> "612","primary immunodeficiency disease","umls","C0021051"
> "612","primary immunodeficiency disease","mondo","0003778"
> "1271","capillary disease","icd10cm","I78"
> "1271","capillary disease","icd10cm","I78.9"
> "1271","capillary disease","icd9cm","448"
> "1271","capillary disease","umls","C0155765"
> "1271","capillary disease","mondo","0001574"
> "1272","telangiectasis","mesh","D013684"
> "1272","telangiectasis","umls","C0039446"
> "1272","telangiectasis","mondo","0001576"
> "1273","respiratory syncytial virus infectious disease","mesh","D018357"
> "1273","respiratory syncytial virus infectious disease","umls","C0035235"
> "1273","respiratory syncytial virus infectious disease","mondo","0001577"
> "614","lymphopenia","icd10cm","D72.810"
> "614","lymphopenia","icd9cm","288.51"
> "614","lymphopenia","mesh","D008231"
> "614","lymphopenia","umls","C0024312"
> "614","lymphopenia","mondo","0003783"
> "615","leukopenia","icd10cm","D72.819"
> "615","leukopenia","icd9cm","288.50"
> "615","leukopenia","mesh","D007970"
> "615","leukopenia","umls","C0023530"
> "615","leukopenia","mondo","0003785"
> "8243","meningeal melanomatosis","umls","C1266114"
> "8243","meningeal melanomatosis","mondo","0004512"
> "8792","eye carcinoma in situ","icd10cm","D09.2"
> "8792","eye carcinoma in situ","icd9cm","234.0"
> "8792","eye carcinoma in situ","umls","C0154094"
> "8792","eye carcinoma in situ","mondo","0004659"
> "10206","lipoma of spermatic cord","icd9cm","214.4"
> "10206","lipoma of spermatic cord","umls","C0153972"
> "10206","lipoma of spermatic cord","mondo","0000975"
> "14218","dihydropyrimidine dehydrogenase deficiency","mesh","D054067"
> "14218","dihydropyrimidine dehydrogenase deficiency","umls","C1959620"
> "14218","dihydropyrimidine dehydrogenase deficiency","umls","C3495551"
> "14218","dihydropyrimidine dehydrogenase deficiency","mondo","0010130"
> "1492","eye and adnexa disease","icd10cm","H35.00"
> "1492","eye and adnexa disease","icd9cm","362.10"
> "1492","eye and adnexa disease","umls","C0004608"
> "1492","eye and adnexa disease","mondo","0002022"
> "0060539","Hermansky-Pudlak syndrome 1","mondo","0008748"
> "0060538","purpura fulminans","icd10cm","D65"
> "0060538","purpura fulminans","mesh","D055665"
> "0060538","purpura fulminans","mondo","0000809"
> "10205","axillary lipoma","umls","C0347429"
> "10205","axillary lipoma","mondo","0000974"
> "0060535","Warsaw breakage syndrome","mondo","0013252"
> "0060534","hepatoid adenocarcinoma","mondo","0006243"
> "0060537","mitochondrial complex II deficiency","icd10cm","G71.3"
> "0060537","mitochondrial complex II deficiency","mesh","C565375"
> "0060537","mitochondrial complex II deficiency","mondo","0009641"
> "0060536","mitochondrial complex I deficiency","mesh","C537475"
> "0060536","mitochondrial complex I deficiency","umls","C2936907"
> "0060536","mitochondrial complex I deficiency","mondo","0009640"
> "8426","follicular infundibulum tumor","umls","C0346006"
> "8426","follicular infundibulum tumor","mondo","0004560"
> "9120","amyloidosis","icd10cm","E85"
> "9120","amyloidosis","icd10cm","E85.9"
> "9120","amyloidosis","icd9cm","277.3"
> "9120","amyloidosis","icd9cm","277.30"
> "9120","amyloidosis","mesh","D000686"
> "9120","amyloidosis","umls","C0002726"
> "9120","amyloidosis","mondo","0019065"
> "1496","echinococcosis","icd10cm","B67"
> "1496","echinococcosis","icd10cm","B67.90"
> "1496","echinococcosis","icd9cm","122"
> "1496","echinococcosis","mesh","D004443"
> "1496","echinococcosis","umls","C0013502"
> "1496","echinococcosis","mondo","0005738"
> "8420","malignant glandular tumor of peripheral nerve sheath","umls","C1333821"
> "8420","malignant glandular tumor of peripheral nerve sheath","mondo","0004559"
> "10201","gallbladder lipoma","umls","C1333747"
> "10201","gallbladder lipoma","mondo","0000972"
> "8428","breast apocrine carcinoma in situ","umls","C1332315"
> "8428","breast apocrine carcinoma in situ","mondo","0004562"
> "1498","cholera","icd10cm","A00"
> "1498","cholera","icd10cm","A00.0"
> "1498","cholera","icd10cm","A00.9"
> "1498","cholera","icd9cm","001"
> "1498","cholera","icd9cm","001.0"
> "1498","cholera","icd9cm","001.9"
> "1498","cholera","mesh","D002771"
> "1498","cholera","umls","C0008354"
> "1498","cholera","mondo","0015766"
> "0070160","atypical hereditary sensory neuropathy","mondo","0009751"
> "9125","lower gum cancer","icd10cm","C03.1"
> "9125","lower gum cancer","icd9cm","143.1"
> "9125","lower gum cancer","umls","C0432581"
> "9125","lower gum cancer","mondo","0004713"
> "9838","cyclotropia","icd10cm","H50.41"
> "9838","cyclotropia","icd9cm","378.33"
> "9838","cyclotropia","umls","C0152209"
> "9838","cyclotropia","mondo","0004894"
> "9839","accommodative esotropia","icd10cm","H50.43"
> "9839","accommodative esotropia","icd9cm","378.35"
> "9839","accommodative esotropia","umls","C0155336"
> "9839","accommodative esotropia","mondo","0004895"
> "7599","lymphoepithelioma-like thymic carcinoma","umls","C0279706"
> "7599","lymphoepithelioma-like thymic carcinoma","mondo","0004297"
> "7598","cervical lymphoepithelioma-like carcinoma","umls","C1516418"
> "7598","cervical lymphoepithelioma-like carcinoma","mondo","0004296"
> "7596","asbestos-related lung carcinoma","umls","C1332337"
> "7596","asbestos-related lung carcinoma","mondo","0004295"
> "3594","choriocarcinoma","icd10cm","C58"
> "3594","choriocarcinoma","mesh","D002822"
> "3594","choriocarcinoma","umls","C0008497"
> "3594","choriocarcinoma","mondo","0005207"
> "9837","hypertropia","icd10cm","H50.2"
> "9837","hypertropia","icd9cm","378.31"
> "9837","hypertropia","mesh","D013285"
> "9837","hypertropia","umls","C0020575"
> "9837","hypertropia","mondo","0004893"
> "7591","gestational ovarian choriocarcinoma","umls","C1517538"
> "7591","gestational ovarian choriocarcinoma","mondo","0004294"
> "9835","refractive error","icd10cm","H52.7"
> "9835","refractive error","mesh","D012030"
> "9835","refractive error","umls","C0034951"
> "9835","refractive error","mondo","0004892"
> "10657","colonic lymphangioma","umls","C1333094"
> "10657","colonic lymphangioma","mondo","0001093"
> "10656","colon leiomyoma","umls","C1333092"
> "10656","colon leiomyoma","mondo","0001092"
> "10651","acute anterolateral myocardial infarction","icd9cm","410.0"
> "10651","acute anterolateral myocardial infarction","umls","C0155627"
> "10651","acute anterolateral myocardial infarction","mondo","0001090"
> "10652","Alzheimer's disease","kegg","05010"
> "10652","Alzheimer's disease","icd10cm","G30"
> "10652","Alzheimer's disease","icd10cm","G30.9"
> "10652","Alzheimer's disease","icd9cm","331.0"
> "10652","Alzheimer's disease","mesh","D000544"
> "10652","Alzheimer's disease","umls","C0002395"
> "10652","Alzheimer's disease","mondo","0004975"
> "4138","bile duct disease","mesh","D001649"
> "4138","bile duct disease","umls","C0005395"
> "4138","bile duct disease","mondo","0002887"
> "4131","erythrasma","icd10cm","L08.1"
> "4131","erythrasma","mesh","D004894"
> "4131","erythrasma","umls","C0014752"
> "4131","erythrasma","mondo","0002885"
> "13326","chronic follicular conjunctivitis","icd10cm","H10.43"
> "13326","chronic follicular conjunctivitis","icd9cm","372.12"
> "13326","chronic follicular conjunctivitis","umls","C0155147"
> "13326","chronic follicular conjunctivitis","mondo","0001685"
> "4136","myxosarcoma","mesh","D009236"
> "4136","myxosarcoma","umls","C0027155"
> "4136","myxosarcoma","mondo","0006863"
> "4137","common bile duct disease","mesh","D003137"
> "4137","common bile duct disease","umls","C0009440"
> "4137","common bile duct disease","mondo","0002886"
> "5692","cellular myxoid liposarcoma","umls","C0334471"
> "5692","cellular myxoid liposarcoma","mondo","0005238"
> "3840","craniopharyngioma","mesh","D003397"
> "3840","craniopharyngioma","umls","C0010276"
> "3840","craniopharyngioma","mondo","0018907"
> "5690","well-differentiated liposarcoma","umls","C1370889"
> "5690","well-differentiated liposarcoma","mondo","0006097"
> "3842","skull base cancer","mesh","D019292"
> "3842","skull base cancer","umls","C0376527"
> "3842","skull base cancer","mondo","0002785"
> "5696","larynx liposarcoma","umls","C1334372"
> "5696","larynx liposarcoma","mondo","0003588"
> "5697","liposarcoma of the ovary","umls","C1335165"
> "5697","liposarcoma of the ovary","mondo","0003589"
> "5694","esophagus liposarcoma","umls","C1333456"
> "5694","esophagus liposarcoma","mondo","0003586"
> "5695","pediatric liposarcoma","umls","C0279984"
> "5695","pediatric liposarcoma","mondo","0003587"
> "5698","fibroblastic liposarcoma","umls","C1266130"
> "5698","fibroblastic liposarcoma","mondo","0003590"
> "5699","kidney liposarcoma","umls","C1335745"
> "5699","kidney liposarcoma","mondo","0003591"
> "0080159","Cryptococcal meningitis","mesh","D016919"
> "0080159","Cryptococcal meningitis","mondo","0005723"
> "0080158","herpes simplex virus keratitis","mesh","D007635"
> "0080158","herpes simplex virus keratitis","mesh","D016849"
> "0080158","herpes simplex virus keratitis","mondo","0015288"
> "0080155","very long chain acyl-CoA dehydrogenase deficiency","mondo","0008723"
> "0080154","short chain acyl-CoA dehydrogenase deficiency","mondo","0008722"
> "0080156","X-linked adrenal hypoplasia congenita","mondo","0010264"
> "0080150","adrenocorticotropic hormone deficiency","mesh","C535668"
> "0080150","adrenocorticotropic hormone deficiency","mondo","0008720"
> "0080153","medium chain acyl-CoA dehydrogenase deficiency","mondo","0008721"
> "13328","diabetic cataract","icd9cm","366.41"
> "13328","diabetic cataract","umls","C0011876"
> "13328","diabetic cataract","mondo","0001687"
> "13329","toxic optic neuropathy","icd10cm","H46.3"
> "13329","toxic optic neuropathy","icd9cm","377.34"
> "13329","toxic optic neuropathy","umls","C0155303"
> "13329","toxic optic neuropathy","mondo","0001688"
> "0111389","mucopolysaccharidosis Ih/s","umls","C0086431"
> "4548","extraskeletal mesenchymal chondrosarcoma","umls","C1275279"
> "4548","extraskeletal mesenchymal chondrosarcoma","mondo","0003043"
> "0090104","Huntington's disease-like 2","icd10cm","G10"
> "0090104","Huntington's disease-like 2","mondo","0011671"
> "4541","nominal aphasia","mesh","D000849"
> "4541","nominal aphasia","umls","C0003113"
> "4541","nominal aphasia","mondo","0003039"
> "4540","dysgraphia","icd10cm","R48.8"
> "4540","dysgraphia","mesh","D000381"
> "4540","dysgraphia","umls","C0001825"
> "4540","dysgraphia","mondo","0003038"
> "4543","retrograde amnesia","icd10cm","R41.2"
> "4543","retrograde amnesia","mesh","D000648"
> "4543","retrograde amnesia","umls","C0002624"
> "4543","retrograde amnesia","mondo","0003040"
> "4542","basophil adenoma","mesh","D000237"
> "4542","basophil adenoma","umls","C0001431"
> "4542","basophil adenoma","mondo","0006673"
> "4545","mesenchymal chondrosarcoma","mesh","D018211"
> "4545","mesenchymal chondrosarcoma","umls","C0206637"
> "4545","mesenchymal chondrosarcoma","mondo","0006853"
> "4547","adult mesenchymal chondrosarcoma","umls","C1332207"
> "4547","adult mesenchymal chondrosarcoma","mondo","0003042"
> "4546","pediatric mesenchymal chondrosarcoma","umls","C1332982"
> "4546","pediatric mesenchymal chondrosarcoma","mondo","0003041"
> "0090079","hypogonadotropic hypogonadism 17 with or without anosmia","icd10cm","E23.0"
> "0090079","hypogonadotropic hypogonadism 17 with or without anosmia","mondo","0014102"
> "0090078","hypogonadotropic hypogonadism 7 with or without anosmia","icd10cm","E23.0"
> "0090078","hypogonadotropic hypogonadism 7 with or without anosmia","mondo","0007794"
> "0090101","lethal congenital glycogen storage disease of heart","icd10cm","E74.0+"
> "0090101","lethal congenital glycogen storage disease of heart","icd10cm","G73.6*"
> "0090101","lethal congenital glycogen storage disease of heart","mondo","0009867"
> "0090073","hypogonadotropic hypogonadism 13 with or without anosmia","icd10cm","E23.0"
> "0090073","hypogonadotropic hypogonadism 13 with or without anosmia","mondo","0013915"
> "0090072","hypogonadotropic hypogonadism 12 with or without anosmia","icd10cm","E23.0"
> "0090072","hypogonadotropic hypogonadism 12 with or without anosmia","mondo","0013914"
> "0090071","hypogonadotropic hypogonadism 11 with or without anosmia","icd10cm","E23.0"
> "0090071","hypogonadotropic hypogonadism 11 with or without anosmia","mondo","0013913"
> "0090070","hypogonadotropic hypogonadism","icd10cm","E23.0"
> "0090070","hypogonadotropic hypogonadism","mondo","0018555"
> "0090077","hypogonadotropic hypogonadism 4 with or without anosmia","icd10cm","E23.0"
> "0090077","hypogonadotropic hypogonadism 4 with or without anosmia","mondo","0012528"
> "0090076","hypogonadotropic hypogonadism 18 with or without anosmia","icd10cm","E23.0"
> "0090076","hypogonadotropic hypogonadism 18 with or without anosmia","mondo","0014103"
> "0090075","hypogonadotropic hypogonadism 15 with or without anosmia","icd10cm","23.0"
> "0090075","hypogonadotropic hypogonadism 15 with or without anosmia","mondo","0013946"
> "0090074","hypogonadotropic hypogonadism 8 with or without anosmia","icd10cm","E23.0"
> "0090074","hypogonadotropic hypogonadism 8 with or without anosmia","mondo","0013910"
> "0050214","Lambert-Eaton myasthenic syndrome","icd10cm","G70.80"
> "0050214","Lambert-Eaton myasthenic syndrome","icd9cm","358.3"
> "0050214","Lambert-Eaton myasthenic syndrome","mesh","D015624"
> "0050214","Lambert-Eaton myasthenic syndrome","umls","C0022972"
> "0050214","Lambert-Eaton myasthenic syndrome","mondo","0018556"
> "1073","renal hypertension","mesh","D006977"
> "1073","renal hypertension","umls","C0020544"
> "1073","renal hypertension","mondo","0001105"
> "2595","glottis cancer","icd10cm","C32.0"
> "2595","glottis cancer","icd9cm","161.0"
> "2595","glottis cancer","umls","C0153483"
> "2595","glottis cancer","mondo","0002351"
> "2596","larynx cancer","icd10cm","C32"
> "2596","larynx cancer","icd10cm","C32.9"
> "2596","larynx cancer","icd9cm","161"
> "2596","larynx cancer","icd9cm","161.9"
> "2596","larynx cancer","mesh","D007822"
> "2596","larynx cancer","umls","C0007107"
> "2596","larynx cancer","mondo","0002352"
> "2597","glottis neoplasm","umls","C0345713"
> "2597","glottis neoplasm","mondo","0002353"
> "2590","familial nephrotic syndrome","icd10cm","N04"
> "2590","familial nephrotic syndrome","mesh","C535761"
> "2590","familial nephrotic syndrome","umls","C3501848"
> "2590","familial nephrotic syndrome","mondo","0002350"
> "2598","laryngeal benign neoplasm","mesh","D007822"
> "2598","laryngeal benign neoplasm","umls","C0023055"
> "2598","laryngeal benign neoplasm","mondo","0002354"
> "2599","glottis carcinoma","umls","C0740083"
> "2599","glottis carcinoma","mondo","0002355"
> "0090109","autosomal dominant hypocalcemia","icd10cm","E20.8"
> "0090109","autosomal dominant hypocalcemia","mondo","0018543"
> "1070","primary open angle glaucoma","icd10cm","H40.11"
> "1070","primary open angle glaucoma","icd9cm","365.11"
> "1070","primary open angle glaucoma","mesh","D005902"
> "1070","primary open angle glaucoma","umls","C0339573"
> "1070","primary open angle glaucoma","mondo","0007665"
> "0060881","renal hypomagnesemia 5 with ocular involvement","mesh","C536148"
> "0060881","renal hypomagnesemia 5 with ocular involvement","umls","C2931121"
> "0060881","renal hypomagnesemia 5 with ocular involvement","mondo","0009548"
> "0060880","renal hypomagnesemia 3","icd10cm","E83.4"
> "0060880","renal hypomagnesemia 3","mondo","0009550"
> "0060883","intestinal hypomagnesemia 1","icd10cm","E83.4"
> "0060883","intestinal hypomagnesemia 1","mondo","0011176"
> "0060882","renal hypomagnesemia 4","icd10cm","E83.4"
> "0060882","renal hypomagnesemia 4","mondo","0012717"
> "0060885","renal hypomagnesemia 2","icd10cm","E83.4"
> "0060885","renal hypomagnesemia 2","mondo","0007937"
> "0060884","renal hypomagnesemia 6","icd10cm","E83.4"
> "0060884","renal hypomagnesemia 6","mondo","0013480"
> "0060887","ossification of the posterior longitudinal ligament of spine","mondo","0011230"
> "0060886","osteopathia striata with cranial sclerosis","mesh","C536053"
> "0060886","osteopathia striata with cranial sclerosis","umls","C0432268"
> "0060886","osteopathia striata with cranial sclerosis","mondo","0010310"
> "0060889","prune belly syndrome","icd10cm","Q79.4"
> "0060889","prune belly syndrome","mesh","D011535"
> "0060889","prune belly syndrome","mondo","0007032"
> "0060888","transient myeloproliferative syndrome","icd10cm","D47.7"
> "0060888","transient myeloproliferative syndrome","mondo","0008040"
> "0110898","inflammatory bowel disease 20","mondo","0012852"
> "0110899","inflammatory bowel disease 28","mondo","0013153"
> "6043","ciliary body spindle cell melanoma","umls","C1333052"
> "6043","ciliary body spindle cell melanoma","mondo","0003746"
> "6041","choroid spindle cell melanoma","umls","C1333027"
> "6041","choroid spindle cell melanoma","mondo","0003745"
> "6048","telangiectatic glomangioma","umls","C1336699"
> "6048","telangiectatic glomangioma","mondo","0003747"
> "2621","autonomic nervous system neoplasm","umls","C1332356"
> "2621","autonomic nervous system neoplasm","mondo","0002366"
> "2626","choroid plexus papilloma","mesh","D020288"
> "2626","choroid plexus papilloma","umls","C0205770"
> "2626","choroid plexus papilloma","umls","C1332963"
> "2626","choroid plexus papilloma","mondo","0009837"
> "0111414","trichohepatoenteric syndrome","mesh","C565627"
> "0111414","trichohepatoenteric syndrome","umls","C1857276"
> "10612","allergic urticaria","icd10cm","L50.0"
> "10612","allergic urticaria","icd9cm","708.0"
> "10612","allergic urticaria","umls","C0149526"
> "10612","allergic urticaria","mondo","0006526"
> "0111418","familial apolipoprotein C-II deficiency","umls","C0268199"
> "0111418","familial apolipoprotein C-II deficiency","umls","C1720779"
> "7350","thymic dysplasia","umls","C1331541"
> "7350","thymic dysplasia","mondo","0004195"
> "9584","Venezuelan equine encephalitis","icd10cm","A92.2"
> "9584","Venezuelan equine encephalitis","icd9cm","066.2"
> "9584","Venezuelan equine encephalitis","mesh","D004685"
> "9584","Venezuelan equine encephalitis","umls","C0014078"
> "9584","Venezuelan equine encephalitis","mondo","0006005"
> "7356","rectum sarcomatoid carcinoma","umls","C1335689"
> "7356","rectum sarcomatoid carcinoma","mondo","0004196"
> "9234","kidney carcinoma in situ","icd10cm","D09.1"
> "9234","kidney carcinoma in situ","icd9cm","233.9"
> "9234","kidney carcinoma in situ","umls","C0154092"
> "9234","kidney carcinoma in situ","mondo","0004732"
> "9235","pyriform sinus cancer","icd10cm","C12"
> "9235","pyriform sinus cancer","icd9cm","148.1"
> "9235","pyriform sinus cancer","umls","C0153400"
> "9235","pyriform sinus cancer","mondo","0004733"
> "9588","encephalitis","mesh","D004660"
> "9588","encephalitis","umls","C0014038"
> "9588","encephalitis","mondo","0019956"
> "9589","urethral calculus","icd10cm","N21.1"
> "9589","urethral calculus","icd9cm","594.2"
> "9589","urethral calculus","umls","C0162301"
> "9589","urethral calculus","mondo","0004826"
> "9230","pompholyx","icd9cm","705.81"
> "9230","pompholyx","mesh","D011146"
> "9230","pompholyx","umls","C0032633"
> "9230","pompholyx","mondo","0006540"
> "10016","multiple endocrine neoplasia type 2B","icd10cm","E31.23"
> "10016","multiple endocrine neoplasia type 2B","icd9cm","258.03"
> "10016","multiple endocrine neoplasia type 2B","mesh","D018814"
> "10016","multiple endocrine neoplasia type 2B","umls","C0025269"
> "10016","multiple endocrine neoplasia type 2B","mondo","0008082"
> "0110098","atopic dermatitis 2","mondo","0011596"
> "0110099","atopic dermatitis 3","mondo","0011597"
> "0110092","short-rib thoracic dysplasia 6 with or without polydactyly","icd10cm","Q77.2"
> "0110092","short-rib thoracic dysplasia 6 with or without polydactyly","mondo","0009894"
> "0110093","short-rib thoracic dysplasia 13 with or without polydactyly","icd10cm","Q77.2"
> "0110093","short-rib thoracic dysplasia 13 with or without polydactyly","mondo","0014577"
> "0110090","short-rib thoracic dysplasia 7 with or without polydactyly","icd10cm","Q77.2"
> "0110090","short-rib thoracic dysplasia 7 with or without polydactyly","mondo","0013569"
> "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","icd10cm","Q77.2"
> "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","icd10cm","Q87.5"
> "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","mondo","0014284"
> "0110096","short-rib thoracic dysplasia 14 with polydactyly","icd10cm","Q04.3"
> "0110096","short-rib thoracic dysplasia 14 with polydactyly","mondo","0014688"
> "0110097","short-rib thoracic dysplasia 9 with or without polydactyly","icd10cm","Q87.5"
> "0110097","short-rib thoracic dysplasia 9 with or without polydactyly","mondo","0009964"
> "0110094","short-rib thoracic dysplasia 8 with or without polydactyly","icd10cm","Q77.2"
> "0110094","short-rib thoracic dysplasia 8 with or without polydactyly","mondo","0014214"
> "0110095","short-rib thoracic dysplasia 11 with or without polydactyly","icd10cm","Q77.2"
> "0110095","short-rib thoracic dysplasia 11 with or without polydactyly","mondo","0014287"
> "12349","primary eye hypotony","icd10cm","H44.44"
> "12349","primary eye hypotony","icd9cm","360.31"
> "12349","primary eye hypotony","umls","C0154782"
> "12349","primary eye hypotony","mondo","0001503"
> "12341","retroperitoneal sarcoma","umls","C0585129"
> "12341","retroperitoneal sarcoma","mondo","0001501"
> "12342","retroperitoneum carcinoma","umls","C0948749"
> "12342","retroperitoneum carcinoma","mondo","0001502"
> "12347","osteogenesis imperfecta","icd10cm","Q78.0"
> "12347","osteogenesis imperfecta","icd9cm","756.51"
> "12347","osteogenesis imperfecta","mesh","D010013"
> "12347","osteogenesis imperfecta","umls","C0023931"
> "12347","osteogenesis imperfecta","umls","C0029434"
> "12347","osteogenesis imperfecta","mondo","0019019"
> "10273","heart conduction disease","icd9cm","426.6"
> "10273","heart conduction disease","umls","C0029630"
> "10273","heart conduction disease","mondo","0000992"
> "10272","left bundle branch hemiblock","icd10cm","I44.60"
> "10272","left bundle branch hemiblock","icd9cm","426.2"
> "10272","left bundle branch hemiblock","umls","C0155702"
> "10272","left bundle branch hemiblock","mondo","0000991"
> "9053","bladder carcinoma in situ","icd10cm","D09.0"
> "9053","bladder carcinoma in situ","icd9cm","233.7"
> "9053","bladder carcinoma in situ","umls","C0154091"
> "9053","bladder carcinoma in situ","mondo","0004703"
> "775","intraocular lymphoma","mesh","D064090"
> "775","intraocular lymphoma","umls","C0281658"
> "775","intraocular lymphoma","mondo","0004351"
> "774","retina lymphoma","umls","C0339556"
> "774","retina lymphoma","mondo","0004349"
> "771","retinal cell cancer","umls","C1335765"
> "771","retinal cell cancer","mondo","0004338"
> "14694","Johanson-Blizzard syndrome","mesh","C535880"
> "14694","Johanson-Blizzard syndrome","umls","C0175692"
> "14694","Johanson-Blizzard syndrome","mondo","0009479"
> "778","delusional disorder","icd10cm","F22"
> "778","delusional disorder","icd9cm","297.1"
> "778","delusional disorder","mesh","D012563"
> "778","delusional disorder","umls","C0011251"
> "778","delusional disorder","mondo","0004359"
> "77","gastrointestinal system disease","icd10cm","K92.9"
> "77","gastrointestinal system disease","icd9cm","520-579.99"
> "77","gastrointestinal system disease","mesh","D004066"
> "77","gastrointestinal system disease","umls","C0012242"
> "77","gastrointestinal system disease","mondo","0004335"
> "0050847","sleep apnea","icd10cm","G47.3"
> "0050847","sleep apnea","icd10cm","G47.30"
> "0050847","sleep apnea","icd9cm","780.57"
> "0050847","sleep apnea","mesh","D012891"
> "0050847","sleep apnea","umls","C0037315"
> "0050847","sleep apnea","mondo","0005296"
> "2978","carbohydrate metabolic disorder","mesh","D002239"
> "2978","carbohydrate metabolic disorder","umls","C0007001"
> "2978","carbohydrate metabolic disorder","mondo","0019214"
> "74","hematopoietic system disease","icd10cm","D75.9"
> "74","hematopoietic system disease","icd9cm","280-289.99"
> "74","hematopoietic system disease","icd9cm","289.9"
> "74","hematopoietic system disease","mesh","D006402"
> "74","hematopoietic system disease","umls","C0018939"
> "74","hematopoietic system disease","mondo","0005570"
> "0050840","cervical dystonia","mondo","0000481"
> "0050841","focal hand dystonia","icd9cm","333.84"
> "0050841","focal hand dystonia","umls","C0154676"
> "0050841","focal hand dystonia","mondo","0000482"
> "2972","renal artery obstruction","icd10cm","N28.0"
> "2972","renal artery obstruction","mesh","D012078"
> "2972","renal artery obstruction","umls","C0035066"
> "2972","renal artery obstruction","mondo","0006945"
> "2973","kidney cortex necrosis","icd10cm","N17.1"
> "2973","kidney cortex necrosis","mesh","D007673"
> "2973","kidney cortex necrosis","umls","C0022656"
> "2973","kidney cortex necrosis","mondo","0006820"
> "2977","primary hyperoxaluria","icd10cm","E72.53"
> "2977","primary hyperoxaluria","mesh","D006959"
> "2977","primary hyperoxaluria","mesh","D006960"
> "2977","primary hyperoxaluria","umls","C0020500"
> "2977","primary hyperoxaluria","umls","C0020501"
> "2977","primary hyperoxaluria","mondo","0002474"
> "0050848","obstructive sleep apnea","icd10cm","G47.33"
> "0050848","obstructive sleep apnea","icd9cm","327.23"
> "0050848","obstructive sleep apnea","mesh","D020181"
> "0050848","obstructive sleep apnea","umls","C0520679"
> "0050848","obstructive sleep apnea","mondo","0007147"
> "2975","cystic kidney disease","mesh","D052177"
> "2975","cystic kidney disease","umls","C0022679"
> "2975","cystic kidney disease","mondo","0002473"
> "5362","focal epithelial hyperplasia","mesh","D017573"
> "5362","focal epithelial hyperplasia","umls","C0206067"
> "5362","focal epithelial hyperplasia","mondo","0009237"
> "5363","myxoid liposarcoma","mesh","D018208"
> "5363","myxoid liposarcoma","umls","C0206634"
> "5363","myxoid liposarcoma","mondo","0013280"
> "1040","chronic lymphocytic leukemia","icd10cm","C91.1"
> "1040","chronic lymphocytic leukemia","icd10cm","C91.10"
> "1040","chronic lymphocytic leukemia","icd9cm","204.1"
> "1040","chronic lymphocytic leukemia","mesh","D015451"
> "1040","chronic lymphocytic leukemia","umls","C0023434"
> "1040","chronic lymphocytic leukemia","mondo","0004948"
> "5364","pulmonary coin lesion","icd10cm","R91.1"
> "5364","pulmonary coin lesion","mesh","D003074"
> "5364","pulmonary coin lesion","umls","C0009250"
> "5364","pulmonary coin lesion","mondo","0006931"
> "5368","Wolffian duct adenocarcinoma","umls","C1516419"
> "5368","Wolffian duct adenocarcinoma","mondo","0003410"
> "4303","sarcomatoid basal cell carcinoma","umls","C1519182"
> "4303","sarcomatoid basal cell carcinoma","mondo","0002957"
> "4301","vulva basal cell carcinoma","umls","C1336977"
> "4301","vulva basal cell carcinoma","mondo","0002955"
> "4300","superficial basal cell carcinoma","umls","C0334256"
> "4300","superficial basal cell carcinoma","mondo","0002954"
> "4307","polyradiculopathy","mesh","D011128"
> "4307","polyradiculopathy","umls","C0032586"
> "4307","polyradiculopathy","mondo","0002960"
> "4306","radiculopathy","icd10cm","M54.1"
> "4306","radiculopathy","icd10cm","M54.10"
> "4306","radiculopathy","mesh","D011843"
> "4306","radiculopathy","umls","C0700594"
> "4306","radiculopathy","mondo","0002959"
> "4305","bone giant cell tumor","mesh","D018212"
> "4305","bone giant cell tumor","umls","C0206638"
> "4305","bone giant cell tumor","mondo","0005674"
> "4304","signet ring basal cell carcinoma","umls","C1519320"
> "4304","signet ring basal cell carcinoma","mondo","0002958"
> "14699","thrombocytopenia-absent radius syndrome","icd10cm","Q87.2"
> "14699","thrombocytopenia-absent radius syndrome","mesh","C536940"
> "14699","thrombocytopenia-absent radius syndrome","umls","C0175703"
> "14699","thrombocytopenia-absent radius syndrome","mondo","0010121"
> "4308","polyradiculoneuropathy","mesh","D011129"
> "4308","polyradiculoneuropathy","umls","C0032587"
> "4308","polyradiculoneuropathy","mondo","0006915"
> "11054","urinary bladder cancer","kegg","05219"
> "11054","urinary bladder cancer","icd10cm","C67"
> "11054","urinary bladder cancer","icd10cm","C67.9"
> "11054","urinary bladder cancer","icd9cm","188"
> "11054","urinary bladder cancer","icd9cm","188.9"
> "11054","urinary bladder cancer","mesh","D001749"
> "11054","urinary bladder cancer","umls","C0005684"
> "11054","urinary bladder cancer","umls","C0005695"
> "11054","urinary bladder cancer","mondo","0001187"
> "11055","pasteurellosis","icd10cm","A28.0"
> "11055","pasteurellosis","icd9cm","027.2"
> "11055","pasteurellosis","mesh","D010326"
> "11055","pasteurellosis","umls","C0030636"
> "11055","pasteurellosis","mondo","0005901"
> "3128","anus disease","mesh","D001004"
> "3128","anus disease","umls","C0003462"
> "3128","anus disease","mondo","0002519"
> "3122","gastric outlet obstruction","mesh","D017219"
> "3122","gastric outlet obstruction","umls","C0162651"
> "3122","gastric outlet obstruction","mondo","0001561"
> "3120","gallbladder papillomatosis","umls","C1333754"
> "3120","gallbladder papillomatosis","mondo","0002518"
> "3121","gallbladder cancer","icd10cm","C23"
> "3121","gallbladder cancer","icd9cm","156.0"
> "3121","gallbladder cancer","mesh","D005706"
> "3121","gallbladder cancer","umls","C0016978"
> "3121","gallbladder cancer","umls","C0153452"
> "3121","gallbladder cancer","umls","C0278806"
> "3121","gallbladder cancer","mondo","0005411"
> "3127","proctitis","icd10cm","K62.89"
> "3127","proctitis","mesh","D011349"
> "3127","proctitis","umls","C0033246"
> "3127","proctitis","mondo","0005538"
> "8659","chickenpox","icd10cm","B01"
> "8659","chickenpox","icd10cm","B01.9"
> "8659","chickenpox","icd9cm","052"
> "8659","chickenpox","mesh","D002644"
> "8659","chickenpox","umls","C0008049"
> "8659","chickenpox","mondo","0005700"
> "8651","Hodgkin's granuloma","icd10cm","C81"
> "8651","Hodgkin's granuloma","icd10cm","C81.0"
> "8651","Hodgkin's granuloma","icd10cm","C81.2"
> "8651","Hodgkin's granuloma","icd10cm","C81.3"
> "8651","Hodgkin's granuloma","icd10cm","C81.4"
> "8651","Hodgkin's granuloma","icd10cm","C81.9"
> "8651","Hodgkin's granuloma","icd9cm","201"
> "8651","Hodgkin's granuloma","icd9cm","201.0"
> "8651","Hodgkin's granuloma","icd9cm","201.1"
> "8651","Hodgkin's granuloma","icd9cm","201.2"
> "8651","Hodgkin's granuloma","icd9cm","201.4"
> "8651","Hodgkin's granuloma","icd9cm","201.6"
> "8651","Hodgkin's granuloma","icd9cm","201.7"
> "8651","Hodgkin's granuloma","icd9cm","201.9"
> "8651","Hodgkin's granuloma","mesh","D006689"
> "8651","Hodgkin's granuloma","umls","C0019829"
> "8651","Hodgkin's granuloma","umls","C0152266"
> "8651","Hodgkin's granuloma","umls","C0152267"
> "8651","Hodgkin's granuloma","umls","C0220597"
> "8651","Hodgkin's granuloma","umls","C1266194"
> "8651","Hodgkin's granuloma","umls","C1334968"
> "8651","Hodgkin's granuloma","mondo","0004632"
> "8654","Hodgkin's lymphoma, mixed cellularity","icd10cm","C81.2"
> "8654","Hodgkin's lymphoma, mixed cellularity","icd9cm","201.6"
> "8654","Hodgkin's lymphoma, mixed cellularity","mesh","D006689"
> "8654","Hodgkin's lymphoma, mixed cellularity","umls","C0152266"
> "8654","Hodgkin's lymphoma, mixed cellularity","mondo","0004633"
> "0060708","lymphoproliferative syndrome 2","icd10cm","D47.9"
> "0060708","lymphoproliferative syndrome 2","mondo","0014054"
> "0060706","X-linked lymphoproliferative syndrome 2","icd10cm","D82.3"
> "0060706","X-linked lymphoproliferative syndrome 2","mondo","0010385"
> "0060707","lymphoproliferative syndrome 1","icd10cm","D47.9"
> "0060707","lymphoproliferative syndrome 1","mondo","0013081"
> "0060704","lymphoproliferative syndrome","mondo","0016537"
> "0060705","X-linked lymphoproliferative syndrome 1","icd10cm","D82.3"
> "0060705","X-linked lymphoproliferative syndrome 1","mondo","0010627"
> "0060702","familial hypocalciuric hypercalcemia 3","icd10cm","E83.5"
> "0060702","familial hypocalciuric hypercalcemia 3","mondo","0010926"
> "0060703","Muenke Syndrome","mesh","C537369"
> "0060703","Muenke Syndrome","umls","C1864436"
> "0060703","Muenke Syndrome","mondo","0011274"
> "0060700","familial hypocalciuric hypercalcemia 1","icd10cm","E83.5"
> "0060700","familial hypocalciuric hypercalcemia 1","mondo","0007791"
> "0060701","familial hypocalciuric hypercalcemia 2","icd10cm","E83.5"
> "0060701","familial hypocalciuric hypercalcemia 2","mondo","0007792"
> "5752","cervical serous adenocarcinoma","umls","C1516431"
> "5752","cervical serous adenocarcinoma","mondo","0003631"
> "5751","pancreatic serous cystadenocarcinoma","umls","C1335315"
> "5751","pancreatic serous cystadenocarcinoma","mondo","0003630"
> "5750","uterine corpus serous adenocarcinoma","umls","C1336921"
> "5750","uterine corpus serous adenocarcinoma","mondo","0003629"
> "5757","endocervicitis","umls","C0014127"
> "5757","endocervicitis","mondo","0003632"
> "5759","sebaceous gland neoplasm","mesh","D012626"
> "5759","sebaceous gland neoplasm","umls","C0036503"
> "5759","sebaceous gland neoplasm","mondo","0006963"
> "5758","malignant mesenchymoma","mesh","C535700"
> "5758","malignant mesenchymoma","umls","C0334492"
> "5758","malignant mesenchymoma","mondo","0003633"
> "863","nervous system disease","icd10cm","G00-G99"
> "863","nervous system disease","icd10cm","G98"
> "863","nervous system disease","icd10cm","G98.8"
> "863","nervous system disease","icd9cm","349.9"
> "863","nervous system disease","mesh","D009422"
> "863","nervous system disease","umls","C0027765"
> "863","nervous system disease","mondo","0005071"
> "3446","anal Paget's disease","umls","C1332274"
> "3446","anal Paget's disease","mondo","0002651"
> "867","maxillary sinus cholesteatoma","umls","C1334644"
> "867","maxillary sinus cholesteatoma","mondo","0006577"
> "0080275","Joubert syndrome 30","mondo","0033308"
> "0111257","gamma-glutamyl transpeptidase deficiency","umls","C0268524"
> "12506","Bell's palsy","icd10cm","G51.0"
> "12506","Bell's palsy","icd9cm","351.0"
> "12506","Bell's palsy","mesh","D020330"
> "12506","Bell's palsy","umls","C0376175"
> "12506","Bell's palsy","mondo","0005665"
> "0111256","hyperferritinemia-cataract syndrome","mesh","C538137"
> "0111256","hyperferritinemia-cataract syndrome","umls","C1833213"
> "0111255","McKusick-Kaufman syndrome","mesh","C538159"
> "0111255","McKusick-Kaufman syndrome","umls","C0948368"
> "7435","polyvesicular vitelline pattern testicular yolk sac tumor","umls","C1515311"
> "7435","polyvesicular vitelline pattern testicular yolk sac tumor","mondo","0004219"
> "7436","sarcomatoid uterine corpus endometrioid adenocarcinoma","umls","C1336913"
> "7436","sarcomatoid uterine corpus endometrioid adenocarcinoma","mondo","0004220"
> "7437","uterus perivascular epithelioid cell tumor","umls","C1519862"
> "7437","uterus perivascular epithelioid cell tumor","mondo","0004221"
> "7430","childhood germ cell brain tumor","umls","C1377598"
> "7430","childhood germ cell brain tumor","mondo","0004218"
> "0111253","neurofibromatosis 1","umls","C0027831"
> "0080273","polycystic kidney disease 5","mondo","0033281"
> "7438","ovarian clear cell cystadenocarcinoma","umls","C0279667"
> "7438","ovarian clear cell cystadenocarcinoma","mondo","0004222"
> "7439","polyp of middle ear","icd10cm","H74.4"
> "7439","polyp of middle ear","umls","C0271466"
> "7439","polyp of middle ear","mondo","0004223"
> "0111252","neurofibromatosis 2","mesh","D016518"
> "0111252","neurofibromatosis 2","umls","C0027832"
> "13636","Fanconi anemia","icd10cm","D61.09"
> "13636","Fanconi anemia","mesh","D005199"
> "13636","Fanconi anemia","umls","C0015625"
> "13636","Fanconi anemia","mondo","0019391"
> "6677","diffuse infiltrative lymphocytosis syndrome","umls","C1333292"
> "6677","diffuse infiltrative lymphocytosis syndrome","mondo","0003963"
> "6676","Froelich syndrome","icd10cm","E23.6"
> "6676","Froelich syndrome","mesh","D007027"
> "6676","Froelich syndrome","umls","C0016724"
> "6676","Froelich syndrome","mondo","0003962"
> "12641","displacement of cardia through esophageal hiatus","icd10cm","Q40.1"
> "12641","displacement of cardia through esophageal hiatus","icd9cm","750.6"
> "12641","displacement of cardia through esophageal hiatus","umls","C0158674"
> "12641","displacement of cardia through esophageal hiatus","mondo","0001562"
> "12642","hiatus hernia","icd10cm","K44"
> "12642","hiatus hernia","mesh","D006551"
> "12642","hiatus hernia","umls","C0267725"
> "12642","hiatus hernia","umls","C0376710"
> "12642","hiatus hernia","umls","C3489393"
> "12642","hiatus hernia","mondo","0007721"
> "6678","tooth and nail syndrome","mesh","C536736"
> "6678","tooth and nail syndrome","umls","C0406735"
> "6678","tooth and nail syndrome","mondo","0008582"
> "2326","gastroenteritis","icd10cm","K52.9"
> "2326","gastroenteritis","mesh","D005759"
> "2326","gastroenteritis","umls","C0017160"
> "2326","gastroenteritis","mondo","0002269"
> "10863","paralytic squint","icd10cm","H49"
> "10863","paralytic squint","icd10cm","H49.9"
> "10863","paralytic squint","icd9cm","378.5"
> "10863","paralytic squint","icd9cm","378.50"
> "10863","paralytic squint","umls","C0152221"
> "10863","paralytic squint","mondo","0001143"
> "10866","total third-nerve palsy","icd9cm","378.52"
> "10866","total third-nerve palsy","mesh","D015840"
> "10866","total third-nerve palsy","umls","C0271371"
> "10866","total third-nerve palsy","mondo","0001145"
> "10864","partial third-nerve palsy","icd9cm","378.51"
> "10864","partial third-nerve palsy","mesh","D015840"
> "10864","partial third-nerve palsy","umls","C0271370"
> "10864","partial third-nerve palsy","mondo","0001144"
> "10865","abducens nerve disease","icd10cm","H49.2"
> "10865","abducens nerve disease","icd9cm","378.54"
> "10865","abducens nerve disease","mesh","C564661"
> "10865","abducens nerve disease","mesh","D020434"
> "10865","abducens nerve disease","umls","C0271355"
> "10865","abducens nerve disease","mondo","0007033"
> "12721","multiple epiphyseal dysplasia","icd9cm","756.56"
> "12721","multiple epiphyseal dysplasia","mesh","D010009"
> "12721","multiple epiphyseal dysplasia","umls","C0026760"
> "12721","multiple epiphyseal dysplasia","mondo","0016648"
> "2368","gangliosidosis","icd10cm","E75.10"
> "2368","gangliosidosis","mesh","D005733"
> "2368","gangliosidosis","umls","C0017083"
> "2368","gangliosidosis","mondo","0017719"
> "2367","neuroaxonal dystrophy","mesh","D019150"
> "2367","neuroaxonal dystrophy","umls","C0338473"
> "2367","neuroaxonal dystrophy","mondo","0002283"
> "2366","West Nile fever","icd10cm","A92.3"
> "2366","West Nile fever","icd10cm","A92.30"
> "2366","West Nile fever","icd9cm","066.4"
> "2366","West Nile fever","icd9cm","066.40"
> "2366","West Nile fever","mesh","D014901"
> "2366","West Nile fever","umls","C0043124"
> "2366","West Nile fever","mondo","0002282"
> "2365","West Nile encephalitis","icd10cm","A92.31"
> "2365","West Nile encephalitis","icd9cm","066.41"
> "2365","West Nile encephalitis","mesh","D014901"
> "2365","West Nile encephalitis","umls","C0751583"
> "2365","West Nile encephalitis","mondo","0019376"
> "2364","post-thrombotic syndrome","icd10cm","I87.0"
> "2364","post-thrombotic syndrome","icd9cm","459.1"
> "2364","post-thrombotic syndrome","mesh","D011186"
> "2364","post-thrombotic syndrome","umls","C0032807"
> "2364","post-thrombotic syndrome","mondo","0005928"
> "2361","macrocytic anemia","mesh","D000748"
> "2361","macrocytic anemia","umls","C0002886"
> "2361","macrocytic anemia","mondo","0002281"
> "0050536","SC phocomelia syndrome","mondo","0010009"
> "0050534","congenital stationary night blindness","icd10cm","H53.63"
> "0050534","congenital stationary night blindness","icd9cm","368.61"
> "0050534","congenital stationary night blindness","mesh","C537743"
> "0050534","congenital stationary night blindness","umls","C1306122"
> "0050534","congenital stationary night blindness","mondo","0016293"
> "0050535","exudative vitreoretinopathy","icd10cm","H35.00"
> "0050535","exudative vitreoretinopathy","icd9cm","362.10"
> "0050535","exudative vitreoretinopathy","umls","C0004608"
> "0050535","exudative vitreoretinopathy","mondo","0019516"
> "0050530","intermediate spinal muscular atrophy","mondo","0009673"
> "5191","stromal predominant kidney Wilms' tumor","umls","C0279610"
> "5191","stromal predominant kidney Wilms' tumor","mondo","0006432"
> "0050538","Charcot-Marie-Tooth disease type 1","mondo","0019011"
> "0050539","Charcot-Marie-Tooth disease type 2","icd9cm","356.0"
> "0050539","Charcot-Marie-Tooth disease type 2","umls","C0392553"
> "0050539","Charcot-Marie-Tooth disease type 2","mondo","0018993"
> "1869","chronic rheumatic pericarditis","icd10cm","I09.2"
> "1869","chronic rheumatic pericarditis","icd9cm","393"
> "1869","chronic rheumatic pericarditis","umls","C0155561"
> "1869","chronic rheumatic pericarditis","mondo","0002133"
> "3720","extramedullary plasmacytoma","icd10cm","C90.2"
> "3720","extramedullary plasmacytoma","icd10cm","C90.20"
> "3720","extramedullary plasmacytoma","umls","C0278619"
> "3720","extramedullary plasmacytoma","mondo","0002754"
> "3721","plasmacytoma","icd10cm","C90.3"
> "3721","plasmacytoma","icd10cm","C90.30"
> "3721","plasmacytoma","mesh","D010954"
> "3721","plasmacytoma","umls","C0032131"
> "3721","plasmacytoma","mondo","0005615"
> "0050026","human monocytic ehrlichiosis","mondo","0000225"
> "3723","solitary plasmacytoma of chest wall","umls","C1332936"
> "3723","solitary plasmacytoma of chest wall","mondo","0002756"
> "4930","nasal cavity adenocarcinoma","umls","C1334920"
> "4930","nasal cavity adenocarcinoma","mondo","0003211"
> "4931","nasal cavity carcinoma","umls","C1377785"
> "4931","nasal cavity carcinoma","mondo","0003212"
> "4932","ampulla of Vater carcinoma","umls","C0262401"
> "4932","ampulla of Vater carcinoma","mondo","0017590"
> "4933","apocrine adenocarcinoma","umls","C0334346"
> "4933","apocrine adenocarcinoma","mondo","0003214"
> "4934","apocrine sweat gland cancer","umls","C1334561"
> "4934","apocrine sweat gland cancer","mondo","0003215"
> "4683","cutaneous mucoepidermoid carcinoma","umls","C0346019"
> "4683","cutaneous mucoepidermoid carcinoma","mondo","0003091"
> "4680","breast metaplastic carcinoma","umls","C1334708"
> "4680","breast metaplastic carcinoma","mondo","0006043"
> "4681","bile duct mucoepidermoid carcinoma","umls","C1332552"
> "4681","bile duct mucoepidermoid carcinoma","mondo","0003089"
> "4938","ureter adenocarcinoma","umls","C1336873"
> "4938","ureter adenocarcinoma","mondo","0003216"
> "4939","ureter carcinoma","umls","C0600079"
> "4939","ureter carcinoma","mondo","0006481"
> "5214","demyelinating polyneuropathy","umls","C0270922"
> "5214","demyelinating polyneuropathy","mondo","0003334"
> "4688","laryngeal mucoepidermoid carcinoma","umls","C1334373"
> "4688","laryngeal mucoepidermoid carcinoma","mondo","0003095"
> "11736","odontoclasia","icd9cm","521.05"
> "11736","odontoclasia","umls","C0341004"
> "11736","odontoclasia","mondo","0001349"
> "2101","vulva squamous cell carcinoma","umls","C0280856"
> "2101","vulva squamous cell carcinoma","mondo","0024609"
> "2106","myotonia congenita","icd9cm","359.22"
> "2106","myotonia congenita","mesh","D009224"
> "2106","myotonia congenita","umls","C0027127"
> "2106","myotonia congenita","mondo","0009710"
> "5117","dermoid cyst of ovary","mesh","C562731"
> "5117","dermoid cyst of ovary","umls","C0237020"
> "5117","dermoid cyst of ovary","mondo","0008167"
> "5113","nutritional deficiency disease","mesh","D003677"
> "5113","nutritional deficiency disease","umls","C0011156"
> "5113","nutritional deficiency disease","mondo","0006873"
> "5112","copper deficiency myelopathy","mesh","D013540"
> "5112","copper deficiency myelopathy","umls","C0038981"
> "5112","copper deficiency myelopathy","mondo","0003280"
> "14159","obstructive hydrocephalus","icd10cm","G91.1"
> "14159","obstructive hydrocephalus","icd9cm","331.4"
> "14159","obstructive hydrocephalus","mesh","D006849"
> "14159","obstructive hydrocephalus","umls","C0549423"
> "14159","obstructive hydrocephalus","mondo","0001896"
> "5119","ovarian cyst","icd10cm","N83.2"
> "5119","ovarian cyst","icd9cm","620.2"
> "5119","ovarian cyst","mesh","D010048"
> "5119","ovarian cyst","umls","C0029513"
> "5119","ovarian cyst","mondo","0003282"
> "5118","ovarian cystic teratoma","umls","C1335155"
> "5118","ovarian cystic teratoma","mondo","0003281"
> "3763","hermaphroditism","mesh","D012734"
> "3763","hermaphroditism","umls","C0019269"
> "3763","hermaphroditism","mondo","0002768"
> "10488","imperforate anus","icd10cm","Q42.3"
> "10488","imperforate anus","mesh","D001006"
> "10488","imperforate anus","umls","C0003466"
> "10488","imperforate anus","mondo","0001046"
> "14150","spinal cord lymphoma","umls","C1336044"
> "14150","spinal cord lymphoma","mondo","0001892"
> "10480","diaphragmatic eventration","icd10cm","Q79.1"
> "10480","diaphragmatic eventration","mesh","D003965"
> "10480","diaphragmatic eventration","umls","C0011981"
> "10480","diaphragmatic eventration","mondo","0006726"
> "10481","diaphragm disease","icd10cm","J98.6"
> "10481","diaphragm disease","icd9cm","519.4"
> "10481","diaphragm disease","umls","C0152097"
> "10481","diaphragm disease","mondo","0005728"
> "10485","esophageal atresia","icd10cm","Q39.0"
> "10485","esophageal atresia","mesh","D004933"
> "10485","esophageal atresia","umls","C0014850"
> "10485","esophageal atresia","mondo","0001044"
> "10486","intestinal atresia","icd10cm","Q41.1"
> "10486","intestinal atresia","mesh","D007409"
> "10486","intestinal atresia","umls","C0021828"
> "10486","intestinal atresia","mondo","0001045"
> "10487","Hirschsprung's disease","icd10cm","Q43.1"
> "10487","Hirschsprung's disease","mesh","D006627"
> "10487","Hirschsprung's disease","umls","C0019569"
> "10487","Hirschsprung's disease","mondo","0018309"
> "890","mitochondrial encephalomyopathy","mesh","D017237"
> "890","mitochondrial encephalomyopathy","umls","C0162666"
> "890","mitochondrial encephalomyopathy","mondo","0004675"
> "891","progressive myoclonus epilepsy","mesh","D020191"
> "891","progressive myoclonus epilepsy","umls","C0751778"
> "891","progressive myoclonus epilepsy","mondo","0020074"
> "893","Wilson disease","icd10cm","E83.01"
> "893","Wilson disease","mesh","D006527"
> "893","Wilson disease","umls","C0019202"
> "893","Wilson disease","mondo","0010200"
> "896","metal metabolism disorder","mesh","D008664"
> "896","metal metabolism disorder","umls","C0025534"
> "896","metal metabolism disorder","mondo","0004689"
> "898","autosomal dominant polycystic kidney disease","icd10cm","Q61.3"
> "898","autosomal dominant polycystic kidney disease","icd9cm","753.12"
> "898","autosomal dominant polycystic kidney disease","mesh","D007690"
> "898","autosomal dominant polycystic kidney disease","umls","C0022680"
> "898","autosomal dominant polycystic kidney disease","mondo","0004691"
> "899","choledochal cyst","icd10cm","Q44.4"
> "899","choledochal cyst","mesh","D015529"
> "899","choledochal cyst","umls","C0008340"
> "899","choledochal cyst","mondo","0018805"
> "0110384","retinitis pigmentosa 25","icd10cm","H35.5"
> "0110384","retinitis pigmentosa 25","mondo","0011272"
> "0110385","retinitis pigmentosa 63","icd10cm","H35.5"
> "0110385","retinitis pigmentosa 63","mondo","0013780"
> "0110823","hereditary spastic paraplegia 8","icd10cm","G11.4"
> "0110823","hereditary spastic paraplegia 8","mondo","0011339"
> "262","kidney hemangiopericytoma","umls","C0346256"
> "262","kidney hemangiopericytoma","mondo","0002365"
> "261","transverse colon cancer","icd10cm","C18.4"
> "261","transverse colon cancer","icd9cm","153.1"
> "261","transverse colon cancer","umls","C0153434"
> "261","transverse colon cancer","mondo","0002361"
> "260","hepatic flexure cancer","icd10cm","C18.3"
> "260","hepatic flexure cancer","icd9cm","153.0"
> "260","hepatic flexure cancer","umls","C0153433"
> "260","hepatic flexure cancer","mondo","0002357"
> "1788","peritoneal mesothelioma","icd10cm","C45.1"
> "1788","peritoneal mesothelioma","umls","C0346109"
> "1788","peritoneal mesothelioma","umls","C0854886"
> "1788","peritoneal mesothelioma","mondo","0005512"
> "1789","benign peritoneal mesothelioma","umls","C1377610"
> "1789","benign peritoneal mesothelioma","mondo","0002112"
> "0110825","hereditary spastic paraplegia 9B","icd10cm","G11.4"
> "0110825","hereditary spastic paraplegia 9B","mondo","0014702"
> "1781","thyroid gland cancer","kegg","05216"
> "1781","thyroid gland cancer","icd10cm","C73"
> "1781","thyroid gland cancer","icd9cm","193"
> "1781","thyroid gland cancer","mesh","D013964"
> "1781","thyroid gland cancer","umls","C0007115"
> "1781","thyroid gland cancer","umls","C0040136"
> "1781","thyroid gland cancer","mondo","0002108"
> "0110824","hereditary spastic paraplegia 9A","icd10cm","G11.4"
> "0110824","hereditary spastic paraplegia 9A","mondo","0011006"
> "1785","pituitary cancer","icd10cm","C75.1"
> "1785","pituitary cancer","mesh","D010911"
> "1785","pituitary cancer","umls","C0032019"
> "1785","pituitary cancer","umls","C0496842"
> "1785","pituitary cancer","mondo","0002109"
> "1786","adrenal rest tumor","mesh","D000314"
> "1786","adrenal rest tumor","umls","C0001630"
> "1786","adrenal rest tumor","mondo","0002110"
> "1787","pericarditis","mesh","D010493"
> "1787","pericarditis","umls","C0031046"
> "1787","pericarditis","mondo","0005904"
> "0110388","retinitis pigmentosa 10","icd10cm","H35.5"
> "0110388","retinitis pigmentosa 10","mondo","0008379"
> "0110389","retinitis pigmentosa 73","icd10cm","H35.5"
> "0110389","retinitis pigmentosa 73","mondo","0014687"
> "6873","skin tag","umls","C0037293"
> "6873","skin tag","mondo","0004026"
> "6872","spinal cord primitive neuroectodermal neoplasm","umls","C1336048"
> "6872","spinal cord primitive neuroectodermal neoplasm","mondo","0006426"
> "6871","spinal cord neuroblastoma","umls","C1336046"
> "6871","spinal cord neuroblastoma","mondo","0004024"
> "0110478","autosomal recessive nonsyndromic deafness 20","icd10cm","H90.3"
> "0110478","autosomal recessive nonsyndromic deafness 20","mondo","0011392"
> "0110828","Usher syndrome type 3","mesh","D052245"
> "0110828","Usher syndrome type 3","umls","C1568248"
> "0110828","Usher syndrome type 3","mondo","0016485"
> "11870","Pick's disease","icd10cm","G31.01"
> "11870","Pick's disease","icd9cm","331.11"
> "11870","Pick's disease","mesh","D020774"
> "11870","Pick's disease","umls","C0236642"
> "11870","Pick's disease","mondo","0008243"
> "11871","macular keratitis","icd10cm","H16.11"
> "11871","macular keratitis","icd9cm","370.22"
> "11871","macular keratitis","umls","C0155076"
> "11871","macular keratitis","mondo","0001395"
> "7390","superior vena cava leiomyosarcoma","umls","C1336531"
> "7390","superior vena cava leiomyosarcoma","mondo","0004208"
> "0110288","autosomal recessive limb-girdle muscular dystrophy type 2W","mondo","0014788"
> "0110287","autosomal recessive limb-girdle muscular dystrophy type 2S","icd10cm","G71.0"
> "0110287","autosomal recessive limb-girdle muscular dystrophy type 2S","mondo","0014144"
> "0110285","autosomal recessive limb-girdle muscular dystrophy type 2Q","icd10cm","G71.0"
> "0110285","autosomal recessive limb-girdle muscular dystrophy type 2Q","mondo","0013390"
> "0110284","autosomal recessive limb-girdle muscular dystrophy type 2L","icd10cm","G71.0"
> "0110284","autosomal recessive limb-girdle muscular dystrophy type 2L","mondo","0012652"
> "0110283","autosomal recessive limb-girdle muscular dystrophy type 2J","icd10cm","G71.0"
> "0110283","autosomal recessive limb-girdle muscular dystrophy type 2J","mondo","0012127"
> "0110282","autosomal recessive limb-girdle muscular dystrophy type 2H","icd10cm","G71.0"
> "0110282","autosomal recessive limb-girdle muscular dystrophy type 2H","mondo","0009683"
> "0110281","autosomal recessive limb-girdle muscular dystrophy type 2G","icd10cm","G71.0"
> "0110281","autosomal recessive limb-girdle muscular dystrophy type 2G","mondo","0011170"
> "0110280","autosomal recessive limb-girdle muscular dystrophy type 2F","icd10cm","G71.0"
> "0110280","autosomal recessive limb-girdle muscular dystrophy type 2F","mondo","0011028"
> "13501","Mobius syndrome","icd10cm","Q87.0"
> "13501","Mobius syndrome","mesh","D020331"
> "13501","Mobius syndrome","umls","C0221060"
> "13501","Mobius syndrome","mondo","0008006"
> "8221","upper clivus meningioma","umls","C1336871"
> "8221","upper clivus meningioma","mondo","0004503"
> "8223","penile urethral cancer","umls","C1518950"
> "8223","penile urethral cancer","mondo","0004504"
> "8224","central breast papilloma","umls","C1332896"
> "8224","central breast papilloma","mondo","0004505"
> "8225","microscopic breast papilloma","umls","C1335390"
> "8225","microscopic breast papilloma","mondo","0004506"
> "8227","atypical breast papilloma","umls","C1332346"
> "8227","atypical breast papilloma","mondo","0004507"
> "674","cleft palate","icd10cm","Q35"
> "674","cleft palate","icd10cm","Q35.9"
> "674","cleft palate","icd9cm","749.0"
> "674","cleft palate","icd9cm","749.00"
> "674","cleft palate","mesh","D002972"
> "674","cleft palate","umls","C0008925"
> "674","cleft palate","mondo","0016064"
> "676","juvenile rheumatoid arthritis","icd10cm","M08.4"
> "676","juvenile rheumatoid arthritis","icd10cm","M08.40"
> "676","juvenile rheumatoid arthritis","icd9cm","714.3"
> "676","juvenile rheumatoid arthritis","icd9cm","714.31"
> "676","juvenile rheumatoid arthritis","icd9cm","714.32"
> "676","juvenile rheumatoid arthritis","icd9cm","714.33"
> "676","juvenile rheumatoid arthritis","umls","C0157916"
> "676","juvenile rheumatoid arthritis","umls","C0157917"
> "676","juvenile rheumatoid arthritis","umls","C0157918"
> "676","juvenile rheumatoid arthritis","umls","C0409667"
> "676","juvenile rheumatoid arthritis","mondo","0011429"
> "11875","denture stomatitis","icd10cm","K12.1"
> "11875","denture stomatitis","mesh","D013282"
> "11875","denture stomatitis","umls","C0038364"
> "11875","denture stomatitis","mondo","0006723"
> "670","amphetamine abuse","icd9cm","305.7"
> "670","amphetamine abuse","mesh","D019969"
> "670","amphetamine abuse","umls","C0154536"
> "670","amphetamine abuse","mondo","0003969"
> "672","spleen cancer","icd10cm","C26.1"
> "672","spleen cancer","mesh","D013160"
> "672","spleen cancer","umls","C0037999"
> "672","spleen cancer","umls","C0153470"
> "672","spleen cancer","mondo","0005966"
> "0060551","poikiloderma with neutropenia","icd10cm","D82.8"
> "0060551","poikiloderma with neutropenia","mesh","C565820"
> "0060551","poikiloderma with neutropenia","mondo","0011405"
> "0060550","ablepharon macrostomia syndrome","mesh","C535557"
> "0060550","ablepharon macrostomia syndrome","umls","C1860224"
> "0060550","ablepharon macrostomia syndrome","mondo","0008693"
> "0060557","ataxia with oculomotor apraxia type 3","mondo","0014084"
> "0060556","Kufor-Rakeb syndrome","mesh","C537177"
> "0060556","Kufor-Rakeb syndrome","umls","C1847640"
> "0060556","Kufor-Rakeb syndrome","mondo","0011706"
> "7609","parathyroid transitional clear cell adenoma","umls","C0279700"
> "7609","parathyroid transitional clear cell adenoma","mondo","0004303"
> "7608","parathyroid adenoma","mesh","D010282"
> "7608","parathyroid adenoma","umls","C0262587"
> "7608","parathyroid adenoma","mondo","0006890"
> "7607","chief cell adenoma","umls","C0334320"
> "7607","chief cell adenoma","mondo","0004302"
> "0060559","lethal congenital contracture syndrome 1","mesh","C537194"
> "0060559","lethal congenital contracture syndrome 1","umls","C1854664"
> "0060559","lethal congenital contracture syndrome 1","mondo","0009670"
> "0060558","lethal congenital contracture syndrome","icd10cm","Q68.8"
> "0060558","lethal congenital contracture syndrome","mondo","0017436"
> "7603","fibrosarcomatous osteosarcoma","umls","C0279602"
> "7603","fibrosarcomatous osteosarcoma","mondo","0004301"
> "7602","intracortical osteogenic sarcoma","umls","C1266166"
> "7602","intracortical osteogenic sarcoma","mondo","0004300"
> "7600","infiltrating bladder lymphoepithelioma-like carcinoma","umls","C1512736"
> "7600","infiltrating bladder lymphoepithelioma-like carcinoma","mondo","0004299"
> "0110476","autosomal recessive nonsyndromic deafness 1B","icd10cm","H90.3"
> "0110476","autosomal recessive nonsyndromic deafness 1B","mondo","0012977"
> "2493","gastric antral vascular ectasia","mesh","D020252"
> "2493","gastric antral vascular ectasia","umls","C0267211"
> "2493","gastric antral vascular ectasia","mondo","0006767"
> "9854","lingual-facial-buccal dyskinesia","icd10cm","G24.4"
> "9854","lingual-facial-buccal dyskinesia","icd9cm","333.82"
> "9854","lingual-facial-buccal dyskinesia","mesh","D020820"
> "9854","lingual-facial-buccal dyskinesia","umls","C0152115"
> "9854","lingual-facial-buccal dyskinesia","mondo","0004901"
> "2497","enamel erosion","icd9cm","521.31"
> "2497","enamel erosion","umls","C1456161"
> "2497","enamel erosion","mondo","0002324"
> "9856","congenital syphilis","icd10cm","A50"
> "9856","congenital syphilis","icd10cm","A50.9"
> "9856","congenital syphilis","icd9cm","090"
> "9856","congenital syphilis","icd9cm","090.9"
> "9856","congenital syphilis","mesh","D013590"
> "9856","congenital syphilis","umls","C0039131"
> "9856","congenital syphilis","mondo","0005714"
> "9857","interstitial keratitis","icd10cm","H16.30"
> "9857","interstitial keratitis","icd9cm","370.50"
> "9857","interstitial keratitis","umls","C0155088"
> "9857","interstitial keratitis","mondo","0004902"
> "9858","deep keratitis","icd10cm","H16.3"
> "9858","deep keratitis","icd9cm","370.5"
> "9858","deep keratitis","umls","C0155087"
> "9858","deep keratitis","mondo","0004903"
> "1525","nodular nonsuppurative panniculitis","icd10cm","M35.6"
> "1525","nodular nonsuppurative panniculitis","mesh","D010201"
> "1525","nodular nonsuppurative panniculitis","umls","C0030328"
> "1525","nodular nonsuppurative panniculitis","mondo","0018063"
> "1254","trichostrongylosis","icd10cm","B81.2"
> "1254","trichostrongylosis","icd9cm","127.6"
> "1254","trichostrongylosis","mesh","D014253"
> "1254","trichostrongylosis","umls","C0040948"
> "1254","trichostrongylosis","mondo","0005995"
> "1255","trichostrongyloidiasis","mesh","D014252"
> "1255","trichostrongyloidiasis","umls","C0040947"
> "1255","trichostrongyloidiasis","mondo","0005994"
> "1520","colon carcinoma","umls","C0699790"
> "1520","colon carcinoma","mondo","0002032"
> "1521","cecum cancer","icd10cm","C18.0"
> "1521","cecum cancer","icd9cm","153.4"
> "1521","cecum cancer","mesh","D002430"
> "1521","cecum cancer","umls","C0153437"
> "1521","cecum cancer","mondo","0002033"
> "1522","cecum lymphoma","umls","C1332867"
> "1522","cecum lymphoma","mondo","0002034"
> "1251","tuberculous epididymitis","icd9cm","016.4"
> "1251","tuberculous epididymitis","umls","C0152814"
> "1251","tuberculous epididymitis","mondo","0001537"
> "1529","penile disease","icd10cm","N48.8"
> "1529","penile disease","icd10cm","N48.89"
> "1529","penile disease","icd9cm","607.8"
> "1529","penile disease","icd9cm","607.89"
> "1529","penile disease","umls","C0029785"
> "1529","penile disease","mondo","0002036"
> "4117","vaginal adenosarcoma","umls","C1519914"
> "4117","vaginal adenosarcoma","mondo","0002881"
> "4114","uterine body mixed cancer","umls","C1334628"
> "4114","uterine body mixed cancer","mondo","0002879"
> "4115","ovarian mesodermal adenosarcoma","umls","C1335169"
> "4115","ovarian mesodermal adenosarcoma","mondo","0002880"
> "4112","cervical carcinosarcoma","umls","C1332917"
> "4112","cervical carcinosarcoma","umls","C1516420"
> "4112","cervical carcinosarcoma","umls","C1518168"
> "4112","cervical carcinosarcoma","mondo","0002877"
> "4113","uterine corpus adenosarcoma","umls","C1336917"
> "4113","uterine corpus adenosarcoma","mondo","0002878"
> "4110","parasitic ectoparasitic infectious disease","mesh","D004478"
> "4110","parasitic ectoparasitic infectious disease","umls","C0013578"
> "4110","parasitic ectoparasitic infectious disease","mondo","0002875"
> "4111","cervical adenosarcoma","umls","C1516426"
> "4111","cervical adenosarcoma","mondo","0002876"
> "4118","colon neuroendocrine neoplasm","umls","C1333097"
> "4118","colon neuroendocrine neoplasm","mondo","0002882"
> "4119","intestinal neuroendocrine benign tumor","umls","C1334231"
> "4119","intestinal neuroendocrine benign tumor","mondo","0002883"
> "9261","nasopharynx carcinoma","icd10cm","C11"
> "9261","nasopharynx carcinoma","icd10cm","C11.0"
> "9261","nasopharynx carcinoma","icd10cm","C11.1"
> "9261","nasopharynx carcinoma","icd10cm","C11.2"
> "9261","nasopharynx carcinoma","icd10cm","C11.3"
> "9261","nasopharynx carcinoma","icd10cm","C11.9"
> "9261","nasopharynx carcinoma","icd9cm","147"
> "9261","nasopharynx carcinoma","icd9cm","147.0"
> "9261","nasopharynx carcinoma","icd9cm","147.1"
> "9261","nasopharynx carcinoma","icd9cm","147.2"
> "9261","nasopharynx carcinoma","icd9cm","147.3"
> "9261","nasopharynx carcinoma","icd9cm","147.9"
> "9261","nasopharynx carcinoma","mesh","D009303"
> "9261","nasopharynx carcinoma","umls","C0153392"
> "9261","nasopharynx carcinoma","umls","C0153393"
> "9261","nasopharynx carcinoma","umls","C0153394"
> "9261","nasopharynx carcinoma","umls","C0153395"
> "9261","nasopharynx carcinoma","umls","C0153396"
> "9261","nasopharynx carcinoma","umls","C0238301"
> "9261","nasopharynx carcinoma","mondo","0015459"
> "5940","malignant peripheral nerve sheath tumor","mesh","D009442"
> "5940","malignant peripheral nerve sheath tumor","umls","C0751690"
> "5940","malignant peripheral nerve sheath tumor","mondo","0017827"
> "11506","suppurative otitis media","icd10cm","H66"
> "11506","suppurative otitis media","icd10cm","H66.4"
> "11506","suppurative otitis media","icd10cm","H66.40"
> "11506","suppurative otitis media","icd9cm","382"
> "11506","suppurative otitis media","icd9cm","382.4"
> "11506","suppurative otitis media","mesh","D010035"
> "11506","suppurative otitis media","umls","C0029888"
> "11506","suppurative otitis media","mondo","0005975"
> "11507","rumination disorder","icd9cm","307.53"
> "11507","rumination disorder","mesh","D019959"
> "11507","rumination disorder","umls","C0154575"
> "11507","rumination disorder","mondo","0001301"
> "11504","autonomic neuropathy","umls","C0259749"
> "11504","autonomic neuropathy","mondo","0001300"
> "11502","mitral valve insufficiency","icd10cm","Q23.3"
> "11502","mitral valve insufficiency","icd9cm","396.3"
> "11502","mitral valve insufficiency","icd9cm","746.6"
> "11502","mitral valve insufficiency","mesh","D008944"
> "11502","mitral valve insufficiency","umls","C0026266"
> "11502","mitral valve insufficiency","umls","C0158619"
> "11502","mitral valve insufficiency","umls","C0264774"
> "11502","mitral valve insufficiency","mondo","0001298"
> "11503","diabetic autonomic neuropathy","mesh","D003929"
> "11503","diabetic autonomic neuropathy","umls","C0271686"
> "11503","diabetic autonomic neuropathy","mondo","0001299"
> "5948","angiokeratoma of mibelli","umls","C0263640"
> "5948","angiokeratoma of mibelli","mondo","0003712"
> "5949","angiokeratoma circumscriptum","umls","C0263638"
> "5949","angiokeratoma circumscriptum","mondo","0003713"
> "980","choroidal sclerosis","icd10cm","H31.1"
> "980","choroidal sclerosis","icd10cm","H31.10"
> "980","choroidal sclerosis","icd9cm","363.4"
> "980","choroidal sclerosis","icd9cm","363.40"
> "980","choroidal sclerosis","mesh","C535358"
> "980","choroidal sclerosis","umls","C0344297"
> "980","choroidal sclerosis","mondo","0004885"
> "9268","glycine encephalopathy","icd10cm","E72.51"
> "9268","glycine encephalopathy","mesh","D020158"
> "9268","glycine encephalopathy","umls","C0751748"
> "9268","glycine encephalopathy","mondo","0011612"
> "10044","balloon cell malignant melanoma","umls","C0334426"
> "10044","balloon cell malignant melanoma","mondo","0000929"
> "0090055","dystonia 25","icd10cm","G24.1"
> "0090055","dystonia 25","mondo","0014033"
> "0090054","episodic kinesigenic dyskinesia 2","icd10cm","G24.8"
> "0090054","episodic kinesigenic dyskinesia 2","mondo","0012603"
> "0090057","X-linked dystonia-parkinsonism","icd10cm","G24.1"
> "0090057","X-linked dystonia-parkinsonism","mondo","0010747"
> "0090056","dystonia 12","icd10cm","G24.1"
> "0090056","dystonia 12","mondo","0007496"
> "0090051","dystonia 23","icd10cm","G24.8"
> "0090051","dystonia 23","mondo","0013928"
> "0090050","dystonia 27","icd10cm","G24.1"
> "0090050","dystonia 27","mondo","0014627"
> "0090053","episodic kinesigenic dyskinesia 1","icd10cm","G24.8"
> "0090053","episodic kinesigenic dyskinesia 1","mondo","0007494"
> "0090052","dystonia 24","icd10cm","G24.8"
> "0090052","dystonia 24","mondo","0014019"
> "0090059","enhanced S-cone syndrome","mesh","C564835"
> "0090059","enhanced S-cone syndrome","mondo","0009989"
> "0060685","autosomal dominant nocturnal frontal lobe epilepsy 4","mondo","0012474"
> "0110917","hereditary spherocytosis type 2","mondo","0000913"
> "0110916","hereditary spherocytosis type 1","mondo","0008447"
> "0110915","childhood hypophosphatasia","mondo","0009428"
> "0110914","infantile hypophosphatasia","mondo","0009427"
> "0110913","adult hypophosphatasia","mondo","0007798"
> "0110912","leukocyte adhesion deficiency 3","mondo","0013016"
> "0110910","leukocyte adhesion deficiency 1","mondo","0007293"
> "0110919","hereditary spherocytosis type 4","mondo","0012981"
> "0110918","hereditary spherocytosis type 3","mondo","0010053"
> "1554","vibratory urticaria","icd10cm","L50.4"
> "1554","vibratory urticaria","icd9cm","708.4"
> "1554","vibratory urticaria","umls","C0157743"
> "1554","vibratory urticaria","mondo","0006618"
> "0110708","hypotrichosis 11","mondo","0014027"
> "0110709","hypotrichosis 12","mondo","0014384"
> "0110878","holoprosencephaly 5","mondo","0012322"
> "0110879","holoprosencephaly 8","mondo","0012267"
> "0110702","hypotrichosis 5","mondo","0013017"
> "0110703","hypotrichosis 6","mondo","0011932"
> "0110700","hypotrichosis 3","mondo","0013514"
> "0110701","hypotrichosis 4","mondo","0007806"
> "0110706","hypotrichosis 9","mondo","0013649"
> "0110707","hypotrichosis 10","mondo","0013650"
> "0110704","hypotrichosis 7","mondo","0011452"
> "0110705","hypotrichosis 8","mondo","0010206"
> "6021","malignant testicular Leydig cell tumor","umls","C1515288"
> "6021","malignant testicular Leydig cell tumor","mondo","0003737"
> "6024","selective IgE deficiency disease","umls","C0398694"
> "6024","selective IgE deficiency disease","mondo","0003738"
> "6025","selective immunoglobulin deficiency disease","umls","C1335942"
> "6025","selective immunoglobulin deficiency disease","mondo","0003739"
> "10071","larynx squamous papilloma","umls","C0240164"
> "10071","larynx squamous papilloma","mondo","0000935"
> "2649","chondroblastoma","mesh","D002804"
> "2649","chondroblastoma","umls","C0008441"
> "2649","chondroblastoma","mondo","0004997"
> "10073","syphilitic meningitis","icd9cm","094.2"
> "10073","syphilitic meningitis","mesh","C536775"
> "10073","syphilitic meningitis","umls","C0153166"
> "10073","syphilitic meningitis","mondo","0000936"
> "10075","diphyllobothriasis","icd10cm","B70.0"
> "10075","diphyllobothriasis","icd9cm","123.4"
> "10075","diphyllobothriasis","mesh","D004169"
> "10075","diphyllobothriasis","umls","C0012561"
> "10075","diphyllobothriasis","mondo","0015260"
> "10074","hymenolepiasis","icd10cm","B71.0"
> "10074","hymenolepiasis","icd9cm","123.6"
> "10074","hymenolepiasis","mesh","D006925"
> "10074","hymenolepiasis","umls","C0020413"
> "10074","hymenolepiasis","mondo","0005802"
> "2640","struma ovarii","mesh","D013330"
> "2640","struma ovarii","umls","C0038478"
> "2640","struma ovarii","mondo","0006980"
> "2641","ovarian germ cell monodermal and highly specialized teratoma","umls","C0280134"
> "2641","ovarian germ cell monodermal and highly specialized teratoma","mondo","0002372"
> "2643","perivascular epithelioid cell tumor","mesh","D054973"
> "2643","perivascular epithelioid cell tumor","umls","C1300127"
> "2643","perivascular epithelioid cell tumor","mondo","0006359"
> "2645","benign mesothelioma","icd10cm","C45"
> "2645","benign mesothelioma","icd10cm","C45.9"
> "2645","benign mesothelioma","mesh","D008654"
> "2645","benign mesothelioma","umls","C0025500"
> "2645","benign mesothelioma","mondo","0002373"
> "2647","parachordoma","umls","C1266175"
> "2647","parachordoma","mondo","0006351"
> "9212","pityriasis rubra pilaris","icd10cm","L44.0"
> "9212","pityriasis rubra pilaris","icd9cm","696.4"
> "9212","pityriasis rubra pilaris","mesh","D010916"
> "9212","pityriasis rubra pilaris","umls","C0032027"
> "9212","pityriasis rubra pilaris","mondo","0008251"
> "9210","herpes zoster oticus","icd10cm","B02.21"
> "9210","herpes zoster oticus","icd9cm","053.11"
> "9210","herpes zoster oticus","mesh","D016697"
> "9210","herpes zoster oticus","umls","C0017409"
> "9210","herpes zoster oticus","mondo","0005769"
> "12365","malaria","icd10cm","B54"
> "12365","malaria","icd9cm","084"
> "12365","malaria","icd9cm","084.6"
> "12365","malaria","mesh","D008288"
> "12365","malaria","umls","C0024530"
> "12365","malaria","mondo","0005136"
> "12364","pulsating exophthalmos","icd10cm","H05.26"
> "12364","pulsating exophthalmos","icd9cm","376.35"
> "12364","pulsating exophthalmos","umls","C0155271"
> "12364","pulsating exophthalmos","mondo","0001513"
> "0050495","exanthema subitum","icd10cm","B08.2"
> "0050495","exanthema subitum","icd10cm","B08.20"
> "0050495","exanthema subitum","icd9cm","058.1"
> "0050495","exanthema subitum","icd9cm","058.10"
> "0050495","exanthema subitum","mesh","D005077"
> "0050495","exanthema subitum","umls","C0015231"
> "0050495","exanthema subitum","mondo","0000337"
> "12362","thyrotoxic exophthalmos","icd9cm","376.21"
> "12362","thyrotoxic exophthalmos","umls","C0155265"
> "12362","thyrotoxic exophthalmos","mondo","0001511"
> "12361","Graves' disease","icd10cm","E05.0"
> "12361","Graves' disease","mesh","D006111"
> "12361","Graves' disease","umls","C0018213"
> "12361","Graves' disease","mondo","0005364"
> "12360","lateral displacement of eye","icd10cm","H05.21"
> "12360","lateral displacement of eye","icd9cm","376.36"
> "12360","lateral displacement of eye","umls","C0155272"
> "12360","lateral displacement of eye","mondo","0001510"
> "12399","pathological gambling","icd10cm","F63.0"
> "12399","pathological gambling","icd9cm","312.31"
> "12399","pathological gambling","mesh","D005715"
> "12399","pathological gambling","umls","C0030662"
> "12399","pathological gambling","mondo","0011662"
> "12369","prolapse of urethra","icd10cm","N81.0"
> "12369","prolapse of urethra","icd9cm","618.03"
> "12369","prolapse of urethra","umls","C0238502"
> "12369","prolapse of urethra","mondo","0001514"
> "9076","discoid lupus erythematosus of eyelid","icd10cm","H01.12"
> "9076","discoid lupus erythematosus of eyelid","icd9cm","373.34"
> "9076","discoid lupus erythematosus of eyelid","umls","C0155180"
> "9076","discoid lupus erythematosus of eyelid","mondo","0004706"
> "9074","systemic lupus erythematosus","kegg","05322"
> "9074","systemic lupus erythematosus","icd10cm","M32"
> "9074","systemic lupus erythematosus","icd10cm","M32.9"
> "9074","systemic lupus erythematosus","icd9cm","710.0"
> "9074","systemic lupus erythematosus","mesh","D008180"
> "9074","systemic lupus erythematosus","umls","C0024141"
> "9074","systemic lupus erythematosus","mondo","0007915"
> "9072","lethal midline granuloma","icd10cm","M31.2"
> "9072","lethal midline granuloma","icd9cm","446.3"
> "9072","lethal midline granuloma","mesh","D006103"
> "9072","lethal midline granuloma","umls","C0018197"
> "9072","lethal midline granuloma","mondo","0006828"
> "0111228","Sveinsson chorioretinal atrophy","umls","C1862382"
> "10290","prostate lymphoma","umls","C1335512"
> "10290","prostate lymphoma","mondo","0000996"
> "10293","monocular esotropia","icd10cm","H50.01"
> "10293","monocular esotropia","icd9cm","378.01"
> "10293","monocular esotropia","mesh","D004948"
> "10293","monocular esotropia","umls","C0152204"
> "10293","monocular esotropia","mondo","0000997"
> "3557","superior mesenteric artery syndrome","mesh","D013478"
> "3557","superior mesenteric artery syndrome","umls","C0038828"
> "3557","superior mesenteric artery syndrome","mondo","0002687"
> "3559","pseudomyxoma peritonei","mesh","D011553"
> "3559","pseudomyxoma peritonei","umls","C0033822"
> "3559","pseudomyxoma peritonei","mondo","0017048"
> "3558","duodenal obstruction","icd10cm","K31.5"
> "3558","duodenal obstruction","mesh","D004380"
> "3558","duodenal obstruction","umls","C0013292"
> "3558","duodenal obstruction","mondo","0002688"
> "2913","acute pancreatitis","icd10cm","K85"
> "2913","acute pancreatitis","icd10cm","K85.9"
> "2913","acute pancreatitis","icd9cm","577.0"
> "2913","acute pancreatitis","umls","C0001339"
> "2913","acute pancreatitis","mondo","0006515"
> "2914","immune system disease","icd10cm","D89.9"
> "2914","immune system disease","icd9cm","279"
> "2914","immune system disease","icd9cm","279.9"
> "2914","immune system disease","umls","C0041806"
> "2914","immune system disease","mondo","0005046"
> "2916","hypersensitivity reaction type IV disease","icd10cm","C88.9"
> "2916","hypersensitivity reaction type IV disease","mesh","D007160"
> "2916","hypersensitivity reaction type IV disease","umls","C0021070"
> "2916","hypersensitivity reaction type IV disease","mondo","0002459"
> "718","autoimmune hemolytic anemia","icd9cm","283.0"
> "718","autoimmune hemolytic anemia","mesh","D000744"
> "718","autoimmune hemolytic anemia","umls","C0002880"
> "718","autoimmune hemolytic anemia","mondo","0020108"
> "715","T-cell leukemia","mesh","D015458"
> "715","T-cell leukemia","umls","C0023492"
> "715","T-cell leukemia","mondo","0005525"
> "713","HCL-V","umls","C0349633"
> "713","HCL-V","mondo","0017600"
> "712","refractory hematologic cancer","umls","C1335724"
> "712","refractory hematologic cancer","mondo","0004111"
> "711","refractory hairy cell leukemia","umls","C0279780"
> "711","refractory hairy cell leukemia","mondo","0004110"
> "710","splenic manifestation of leukemia","umls","C1336065"
> "710","splenic manifestation of leukemia","mondo","0004107"
> "0050820","atrioventricular block","icd10cm","I44.3"
> "0050820","atrioventricular block","icd10cm","I44.30"
> "0050820","atrioventricular block","icd9cm","426.10"
> "0050820","atrioventricular block","mesh","D054537"
> "0050820","atrioventricular block","umls","C0004245"
> "0050820","atrioventricular block","mondo","0000465"
> "0050826","tricuspid valve disease","icd10cm","I07"
> "0050826","tricuspid valve disease","icd10cm","I07.9"
> "0050826","tricuspid valve disease","icd9cm","397.0"
> "0050826","tricuspid valve disease","umls","C0264776"
> "0050826","tricuspid valve disease","mondo","0000471"
> "5308","ampulla of Vater clear cell adenocarcinoma","umls","C1332246"
> "5308","ampulla of Vater clear cell adenocarcinoma","mondo","0003388"
> "5309","epithelial-myoepithelial carcinoma","umls","C0334392"
> "5309","epithelial-myoepithelial carcinoma","mondo","0003389"
> "5301","fallopian tube clear cell adenocarcinoma","umls","C1333591"
> "5301","fallopian tube clear cell adenocarcinoma","mondo","0003383"
> "5302","uterine ligament clear cell adenocarcinoma","umls","C1519867"
> "5302","uterine ligament clear cell adenocarcinoma","mondo","0003384"
> "5303","cervical clear cell adenocarcinoma","umls","C1332912"
> "5303","cervical clear cell adenocarcinoma","mondo","0006135"
> "5304","ovarian clear cell adenocarcinoma","umls","C1518693"
> "5304","ovarian clear cell adenocarcinoma","mondo","0006045"
> "1064","cystinosis","mesh","D003554"
> "1064","cystinosis","umls","C2931187"
> "1064","cystinosis","mondo","0016239"
> "5306","bladder clear cell adenocarcinoma","umls","C1332557"
> "5306","bladder clear cell adenocarcinoma","mondo","0003386"
> "5307","urethra clear cell adenocarcinoma","umls","C1336886"
> "5307","urethra clear cell adenocarcinoma","mondo","0003387"
> "13014","shipyard eye","icd10cm","B30.0"
> "13014","shipyard eye","icd9cm","077.1"
> "13014","shipyard eye","umls","C0014493"
> "13014","shipyard eye","mondo","0001615"
> "4329","Erdheim-Chester disease","mesh","D031249"
> "4329","Erdheim-Chester disease","umls","C0878675"
> "4329","Erdheim-Chester disease","mondo","0018153"
> "4321","large cell acanthoma","umls","C1334362"
> "4321","large cell acanthoma","mondo","0002961"
> "4320","non-gestational choriocarcinoma","mesh","D031954"
> "4320","non-gestational choriocarcinoma","umls","C1135873"
> "4320","non-gestational choriocarcinoma","mondo","0006871"
> "4323","epidermolytic acanthoma","umls","C1333414"
> "4323","epidermolytic acanthoma","mondo","0002962"
> "4322","pilar sheath acanthoma","mesh","D049309"
> "4322","pilar sheath acanthoma","umls","C0346005"
> "4322","pilar sheath acanthoma","mondo","0006907"
> "4325","Ebola hemorrhagic fever","icd10cm","A98.4"
> "4325","Ebola hemorrhagic fever","mesh","D019142"
> "4325","Ebola hemorrhagic fever","umls","C0282687"
> "4325","Ebola hemorrhagic fever","mondo","0005737"
> "4324","acantholytic acanthoma","umls","C1301270"
> "4324","acantholytic acanthoma","mondo","0002963"
> "4327","Marburg hemorrhagic fever","icd10cm","A98.3"
> "4327","Marburg hemorrhagic fever","mesh","D008379"
> "4327","Marburg hemorrhagic fever","umls","C0024788"
> "4327","Marburg hemorrhagic fever","mondo","0020500"
> "3140","scleredema adultorum","mesh","D012592"
> "3140","scleredema adultorum","umls","C0036413"
> "3140","scleredema adultorum","mondo","0006606"
> "3141","mucinoses","mesh","D017520"
> "3141","mucinoses","umls","C0162855"
> "3141","mucinoses","mondo","0002523"
> "3142","leg dermatosis","mesh","D007868"
> "3142","leg dermatosis","umls","C0023219"
> "3142","leg dermatosis","mondo","0006569"
> "3144","cutis laxa","icd10cm","Q82.8"
> "3144","cutis laxa","mesh","D003483"
> "3144","cutis laxa","umls","C0010495"
> "3144","cutis laxa","mondo","0016175"
> "3145","hyperlipoproteinemia type III","mesh","D006952"
> "3145","hyperlipoproteinemia type III","umls","C0020479"
> "3145","hyperlipoproteinemia type III","mondo","0018473"
> "3146","lipid metabolism disorder","mesh","D008052"
> "3146","lipid metabolism disorder","umls","C0023772"
> "3146","lipid metabolism disorder","mondo","0002525"
> "1526","panniculitis","icd10cm","M79.3"
> "1526","panniculitis","icd9cm","729.3"
> "1526","panniculitis","icd9cm","729.30"
> "1526","panniculitis","mesh","D015434"
> "1526","panniculitis","umls","C0030326"
> "1526","panniculitis","mondo","0006591"
> "3148","dermal unilateral segmental cavernous angioma","umls","C0474966"
> "3148","dermal unilateral segmental cavernous angioma","mondo","0002526"
> "3149","keratoacanthoma","mesh","D007636"
> "3149","keratoacanthoma","umls","C0022572"
> "3149","keratoacanthoma","mondo","0002527"
> "0060768","Smith-Magenis syndrome","icd10cm","Q93.5"
> "0060768","Smith-Magenis syndrome","mesh","D058496"
> "0060768","Smith-Magenis syndrome","mondo","0008434"
> "0060769","T-cell immunodeficiency, congenital alopecia, and nail dystrophy","icd10cm","D82.8"
> "0060769","T-cell immunodeficiency, congenital alopecia, and nail dystrophy","mondo","0011132"
> "0060760","immunodeficiency with hyper-IgM type 4","icd10cm","D80.5"
> "0060760","immunodeficiency with hyper-IgM type 4","mondo","0011985"
> "0060761","familial chronic myelocytic leukemia-like syndrome","mondo","0010809"
> "0060762","lethal restrictive dermopathy","mesh","C536920"
> "0060762","lethal restrictive dermopathy","umls","C0406585"
> "0060762","lethal restrictive dermopathy","mondo","0010143"
> "0060763","X-linked juvenile retinoschisis 1","icd10cm","Q14.1"
> "0060763","X-linked juvenile retinoschisis 1","mondo","0010725"
> "0060764","autosomal recessive Robinow syndrome","mondo","0009999"
> "0060765","autosomal dominant Robinow syndrome 2","mondo","0014591"
> "0060766","autosomal dominant Robinow syndrome 1","mondo","0024455"
> "0060767","autosomal dominant Robinow syndrome 3","mondo","0014819"
> "5773","oral submucous fibrosis","icd10cm","K13.5"
> "5773","oral submucous fibrosis","icd9cm","528.8"
> "5773","oral submucous fibrosis","mesh","D009914"
> "5773","oral submucous fibrosis","umls","C0029171"
> "5773","oral submucous fibrosis","umls","C0029172"
> "5773","oral submucous fibrosis","mondo","0018166"
> "5772","central nervous system hematologic cancer","umls","C1332882"
> "5772","central nervous system hematologic cancer","mondo","0003641"
> "5775","cavernous hemangioma of colon","umls","C1333086"
> "5775","cavernous hemangioma of colon","mondo","0003644"
> "5774","giant hemangioma","umls","C1333817"
> "5774","giant hemangioma","mondo","0003643"
> "5777","rectum neuroendocrine neoplasm","umls","C1335686"
> "5777","rectum neuroendocrine neoplasm","mondo","0003646"
> "5776","cavernous hemangioma of face","umls","C1332863"
> "5776","cavernous hemangioma of face","mondo","0003645"
> "2060","vulvar nodular hidradenoma","umls","C1520091"
> "2060","vulvar nodular hidradenoma","mondo","0002188"
> "12568","dyscalculia","mesh","D060705"
> "12568","dyscalculia","mondo","0001552"
> "12566","ulceration of vulva","icd10cm","N77.0"
> "12566","ulceration of vulva","icd9cm","616.51"
> "12566","ulceration of vulva","umls","C0156340"
> "12566","ulceration of vulva","mondo","0001551"
> "7411","ovarian endometrioid cystadenofibroma","umls","C1335158"
> "7411","ovarian endometrioid cystadenofibroma","mondo","0004214"
> "6613","vaginal villous adenoma","umls","C1519936"
> "6613","vaginal villous adenoma","mondo","0003946"
> "6612","leukocyte adhesion deficiency","mesh","D018370"
> "6612","leukocyte adhesion deficiency","umls","C0242597"
> "6612","leukocyte adhesion deficiency","mondo","0017570"
> "6610","bone epithelioid hemangioma","umls","C1332575"
> "6610","bone epithelioid hemangioma","umls","C1332578"
> "6610","bone epithelioid hemangioma","mondo","0003945"
> "10841","Eastern equine encephalitis","icd10cm","A83.2"
> "10841","Eastern equine encephalitis","icd9cm","062.2"
> "10841","Eastern equine encephalitis","mesh","D020242"
> "10841","Eastern equine encephalitis","umls","C0153065"
> "10841","Eastern equine encephalitis","mondo","0005736"
> "10842","Murray Valley encephalitis","icd10cm","A83.4"
> "10842","Murray Valley encephalitis","icd9cm","062.4"
> "10842","Murray Valley encephalitis","umls","C0153066"
> "10842","Murray Valley encephalitis","mondo","0001137"
> "10843","Western equine encephalitis","icd10cm","A83.1"
> "10843","Western equine encephalitis","icd9cm","062.1"
> "10843","Western equine encephalitis","mesh","D020241"
> "10843","Western equine encephalitis","umls","C0153064"
> "10843","Western equine encephalitis","mondo","0019380"
> "10844","Japanese encephalitis","icd10cm","A83.0"
> "10844","Japanese encephalitis","icd9cm","062.0"
> "10844","Japanese encephalitis","mesh","D004672"
> "10844","Japanese encephalitis","umls","C0014057"
> "10844","Japanese encephalitis","mondo","0019209"
> "10845","St. Louis encephalitis","icd10cm","A83.3"
> "10845","St. Louis encephalitis","icd9cm","062.3"
> "10845","St. Louis encephalitis","mesh","D004674"
> "10845","St. Louis encephalitis","umls","C0014060"
> "10845","St. Louis encephalitis","mondo","0005969"
> "10846","angiodysplasia of intestine","icd9cm","569.84"
> "10846","angiodysplasia of intestine","umls","C0267367"
> "10846","angiodysplasia of intestine","mondo","0001138"
> "10849","sexual masochism","icd10cm","F65.51"
> "10849","sexual masochism","icd9cm","302.83"
> "10849","sexual masochism","mesh","D008398"
> "10849","sexual masochism","umls","C0036908"
> "10849","sexual masochism","mondo","0001139"
> "3500","gallbladder adenocarcinoma","umls","C0279651"
> "3500","gallbladder adenocarcinoma","mondo","0006215"
> "3501","ampullary signet ring cell adenocarcinoma","umls","C1332249"
> "3501","ampullary signet ring cell adenocarcinoma","mondo","0002669"
> "0080292","retinitis pigmentosa 81","mondo","0036482"
> "0080293","short-rib thoracic dysplasia 18 with polydactyly","mondo","0036483"
> "0080290","familial erythrocytosis 5","mondo","0033483"
> "0080291","early infantile epileptic encephalopathy 59","mondo","0033368"
> "0080296","hypomyelinating leukodystrophy 14","mondo","0033486"
> "0080297","Coffin-Siris syndrome 6","mondo","0033492"
> "0080294","Charcot-Marie-Tooth disease dominant intermediate G","mondo","0036484"
> "0080295","short-rib thoracic dysplasia 19 with or without polydactyly","mondo","0033485"
> "12190","descending colon cancer","icd10cm","C18.6"
> "12190","descending colon cancer","icd9cm","153.2"
> "12190","descending colon cancer","umls","C0153435"
> "12190","descending colon cancer","mondo","0001462"
> "12191","splenic flexure cancer","icd10cm","C18.5"
> "12191","splenic flexure cancer","icd9cm","153.7"
> "12191","splenic flexure cancer","umls","C0153440"
> "12191","splenic flexure cancer","mondo","0001463"
> "12192","sigmoid colon cancer","icd10cm","C18.7"
> "12192","sigmoid colon cancer","icd9cm","153.3"
> "12192","sigmoid colon cancer","mesh","D012811"
> "12192","sigmoid colon cancer","umls","C0153436"
> "12192","sigmoid colon cancer","mondo","0001464"
> "12196","superficial keratitis","icd10cm","H16.10"
> "12196","superficial keratitis","icd9cm","370.20"
> "12196","superficial keratitis","umls","C0155074"
> "12196","superficial keratitis","mondo","0001465"
> "12197","punctate epithelial keratoconjunctivitis","icd10cm","H16.14"
> "12197","punctate epithelial keratoconjunctivitis","icd9cm","370.21"
> "12197","punctate epithelial keratoconjunctivitis","umls","C0259799"
> "12197","punctate epithelial keratoconjunctivitis","mondo","0001466"
> "2345","plasma protein metabolism disease","icd9cm","273.8"
> "2345","plasma protein metabolism disease","umls","C0029594"
> "2345","plasma protein metabolism disease","mondo","0002273"
> "2344","polyclonal hypergammaglobulinemia","icd10cm","D89.0"
> "2344","polyclonal hypergammaglobulinemia","icd9cm","273.0"
> "2344","polyclonal hypergammaglobulinemia","umls","C0154254"
> "2344","polyclonal hypergammaglobulinemia","mondo","0002272"
> "2347","generalized atherosclerosis","icd10cm","I70.91"
> "2347","generalized atherosclerosis","icd9cm","440.9"
> "2347","generalized atherosclerosis","umls","C0017327"
> "2347","generalized atherosclerosis","mondo","0002275"
> "2346","monoclonal paraproteinemia","icd9cm","273.1"
> "2346","monoclonal paraproteinemia","umls","C0026471"
> "2346","monoclonal paraproteinemia","mondo","0002274"
> "2340","craniosynostosis","icd10cm","Q75.0"
> "2340","craniosynostosis","mesh","D003398"
> "2340","craniosynostosis","umls","C0010278"
> "2340","craniosynostosis","mondo","0015469"
> "2349","arteriosclerosis","icd10cm","I70"
> "2349","arteriosclerosis","mesh","D001161"
> "2349","arteriosclerosis","umls","C0003850"
> "2349","arteriosclerosis","mondo","0002277"
> "2348","arteriosclerotic cardiovascular disease","icd10cm","I25.1"
> "2348","arteriosclerotic cardiovascular disease","icd10cm","I70"
> "2348","arteriosclerotic cardiovascular disease","icd9cm","440"
> "2348","arteriosclerotic cardiovascular disease","mesh","D050197"
> "2348","arteriosclerotic cardiovascular disease","umls","C0004153"
> "2348","arteriosclerotic cardiovascular disease","umls","C3665365"
> "2348","arteriosclerotic cardiovascular disease","mondo","0002277"
> "0111446","progressive myoclonus epilepsy 3","umls","C2673257"
> "0080116","mitochondrial complex III deficiency nuclear type 7","mondo","0014356"
> "0111447","progressive myoclonus epilepsy 7","umls","C4015420"
> "0050554","X-linked sideroblastic anemia with ataxia","mondo","0010524"
> "0111444","progressive myoclonus epilepsy 4","umls","C0751779"
> "0050004","seminal vesicle acute gonorrhea","umls","C0578661"
> "0050004","seminal vesicle acute gonorrhea","mondo","0000222"
> "0050557","congenital muscular dystrophy","icd9cm","359.0"
> "0050557","congenital muscular dystrophy","umls","C2937300"
> "0050557","congenital muscular dystrophy","mondo","0019950"
> "0050558","Ullrich congenital muscular dystrophy","mondo","0000355"
> "0050559","Fukuyama congenital muscular dystrophy","mondo","0009678"
> "3709","rectum mucinous adenocarcinoma","umls","C0279652"
> "3709","rectum mucinous adenocarcinoma","mondo","0002748"
> "3703","prostate colloid adenocarcinoma","umls","C1335513"
> "3703","prostate colloid adenocarcinoma","mondo","0006067"
> "0080474","pustular psoriasis 14","icd10cm","L40.1"
> "3707","endometrial mucinous adenocarcinoma","umls","C1519859"
> "3707","endometrial mucinous adenocarcinoma","mondo","0002747"
> "3705","fallopian tube mucinous tumor","umls","C1517120"
> "3705","fallopian tube mucinous tumor","mondo","0002745"
> "2121","ectodermal dysplasia","mesh","D004476"
> "2121","ectodermal dysplasia","mondo","0019287"
> "2120","focal dermal hypoplasia","mesh","D005489"
> "2120","focal dermal hypoplasia","umls","C0016395"
> "2120","focal dermal hypoplasia","mondo","0010592"
> "2123","tularemia","icd9cm","021.8"
> "2123","tularemia","umls","C0029835"
> "2123","tularemia","mondo","0018077"
> "2122","pneumonic tularemia","icd10cm","A21.2"
> "2122","pneumonic tularemia","icd9cm","021.2"
> "2122","pneumonic tularemia","umls","C0339946"
> "2122","pneumonic tularemia","mondo","0002212"
> "13579","kwashiorkor","icd10cm","E40"
> "13579","kwashiorkor","icd9cm","260"
> "13579","kwashiorkor","mesh","D007732"
> "13579","kwashiorkor","umls","C0022806"
> "13579","kwashiorkor","mondo","0006826"
> "2127","brain germinoma","umls","C1332606"
> "2127","brain germinoma","mondo","0002214"
> "4919","renal pelvis carcinoma","icd10cm","C65"
> "4919","renal pelvis carcinoma","icd9cm","189.1"
> "4919","renal pelvis carcinoma","umls","C0153618"
> "4919","renal pelvis carcinoma","umls","C1335749"
> "4919","renal pelvis carcinoma","mondo","0005519"
> "4664","filamentary keratitis","icd10cm","H16.12"
> "4664","filamentary keratitis","icd9cm","370.23"
> "4664","filamentary keratitis","umls","C0155077"
> "4664","filamentary keratitis","mondo","0003082"
> "4917","villous adenocarcinoma","umls","C0334306"
> "4917","villous adenocarcinoma","mondo","0003204"
> "4914","esophagus adenocarcinoma","mesh","C562730"
> "4914","esophagus adenocarcinoma","umls","C0279628"
> "4914","esophagus adenocarcinoma","mondo","0005028"
> "4915","basophilic adenocarcinoma","umls","C0334314"
> "4915","basophilic adenocarcinoma","mondo","0003202"
> "4660","indolent systemic mastocytosis","icd10cm","D47.02"
> "4660","indolent systemic mastocytosis","mesh","D034721"
> "4660","indolent systemic mastocytosis","umls","C0272203"
> "4660","indolent systemic mastocytosis","mondo","0020331"
> "4661","multiple chemical sensitivity","mesh","D018777"
> "4661","multiple chemical sensitivity","umls","C0242992"
> "4661","multiple chemical sensitivity","mondo","0005862"
> "4662","thalamic disease","mesh","D013786"
> "4662","thalamic disease","umls","C0039726"
> "4662","thalamic disease","mondo","0003081"
> "11713","diabetic angiopathy","mesh","D003925"
> "11713","diabetic angiopathy","umls","C0011875"
> "11713","diabetic angiopathy","mondo","0000960"
> "2226","myeloproliferative neoplasm","icd10cm","D47.1"
> "2226","myeloproliferative neoplasm","umls","C1292778"
> "2226","myeloproliferative neoplasm","mondo","0020076"
> "6445","ovarian endometrioid malignant adenofibroma","umls","C1518711"
> "6445","ovarian endometrioid malignant adenofibroma","mondo","0003879"
> "11717","neonatal diabetes mellitus","icd10cm","P70.2"
> "11717","neonatal diabetes mellitus","icd9cm","775.1"
> "11717","neonatal diabetes mellitus","umls","C0158981"
> "11717","neonatal diabetes mellitus","mondo","0016391"
> "11716","prediabetes syndrome","icd10cm","R73.03"
> "11716","prediabetes syndrome","mesh","D011236"
> "11716","prediabetes syndrome","umls","C0362046"
> "11716","prediabetes syndrome","mondo","0006920"
> "11714","gestational diabetes","icd10cm","O24.4"
> "11714","gestational diabetes","mesh","D016640"
> "11714","gestational diabetes","umls","C0085207"
> "11714","gestational diabetes","mondo","0005406"
> "11719","oculopharyngeal muscular dystrophy","icd10cm","G71.0"
> "11719","oculopharyngeal muscular dystrophy","mesh","D039141"
> "11719","oculopharyngeal muscular dystrophy","umls","C0270952"
> "11719","oculopharyngeal muscular dystrophy","mondo","0008116"
> "0110136","Bardet-Biedl syndrome 14","icd10cm","Q87.89"
> "0110136","Bardet-Biedl syndrome 14","mondo","0014442"
> "2224","essential thrombocythemia","icd10cm","D47.3"
> "2224","essential thrombocythemia","icd9cm","238.71"
> "2224","essential thrombocythemia","mesh","D013920"
> "2224","essential thrombocythemia","umls","C0040028"
> "2224","essential thrombocythemia","mondo","0005029"
> "5172","endometrium carcinoma in situ","icd10cm","D07.0"
> "5172","endometrium carcinoma in situ","umls","C0346191"
> "5172","endometrium carcinoma in situ","mondo","0003315"
> "5171","vaginal endometrial stromal tumor","umls","C4289585"
> "5171","vaginal endometrial stromal tumor","mondo","0003314"
> "5170","vaginal endometrial stromal sarcoma","umls","C3642329"
> "5170","vaginal endometrial stromal sarcoma","mondo","0003313"
> "5176","renal Wilms' tumor","umls","C1335062"
> "5176","renal Wilms' tumor","mondo","0019004"
> "2222","factor X deficiency","mesh","D005171"
> "2222","factor X deficiency","umls","C0015519"
> "2222","factor X deficiency","mondo","0009212"
> "5179","mixed cell type kidney Wilms' tumor","umls","C0279611"
> "5179","mixed cell type kidney Wilms' tumor","mondo","0003318"
> "5178","metachronous kidney Wilms' tumor","umls","C1334705"
> "5178","metachronous kidney Wilms' tumor","mondo","0003317"
> "2223","platelet storage pool deficiency","mesh","D010981"
> "2223","platelet storage pool deficiency","umls","C0032197"
> "2223","platelet storage pool deficiency","mondo","0008495"
> "133","vaginal Mullerian papilloma","umls","C1519926"
> "133","vaginal Mullerian papilloma","mondo","0001680"
> "137","vaginal squamous papilloma","umls","C1336943"
> "137","vaginal squamous papilloma","mondo","0001779"
> "136","vaginal carcinosarcoma","umls","C1512974"
> "136","vaginal carcinosarcoma","umls","C1519918"
> "136","vaginal carcinosarcoma","umls","C1519924"
> "136","vaginal carcinosarcoma","mondo","0006488"
> "135","benign vaginal carcinosarcoma","umls","C1511106"
> "135","benign vaginal carcinosarcoma","mondo","0001731"
> "134","vaginal glandular tumor","umls","C1519921"
> "134","vaginal glandular tumor","mondo","0001704"
> "139","squamous cell papilloma","mesh","D010212"
> "139","squamous cell papilloma","umls","C0205874"
> "139","squamous cell papilloma","mondo","0001825"
> "138","vaginal squamous tumor","umls","C1519931"
> "138","vaginal squamous tumor","mondo","0001806"
> "13924","necrotizing ulcerative gingivitis","icd10cm","A69.1"
> "13924","necrotizing ulcerative gingivitis","icd9cm","101"
> "13924","necrotizing ulcerative gingivitis","mesh","D005892"
> "13924","necrotizing ulcerative gingivitis","umls","C0017575"
> "13924","necrotizing ulcerative gingivitis","umls","C1527368"
> "13924","necrotizing ulcerative gingivitis","mondo","0006865"
> "13922","eosinophilic esophagitis","icd10cm","K20.0"
> "13922","eosinophilic esophagitis","icd9cm","530.13"
> "13922","eosinophilic esophagitis","mesh","D057765"
> "13922","eosinophilic esophagitis","umls","C0341106"
> "13922","eosinophilic esophagitis","mondo","0005361"
> "0110319","hypertrophic cardiomyopathy 13","mondo","0013195"
> "0110318","hypertrophic cardiomyopathy 12","mondo","0012804"
> "9681","cervical incompetence","icd10cm","N88.3"
> "9681","cervical incompetence","icd9cm","622.5"
> "9681","cervical incompetence","mesh","D002581"
> "9681","cervical incompetence","umls","C0007871"
> "9681","cervical incompetence","mondo","0005698"
> "9682","yellow fever","icd10cm","A95"
> "9682","yellow fever","icd10cm","A95.9"
> "9682","yellow fever","icd9cm","060"
> "9682","yellow fever","icd9cm","060.9"
> "9682","yellow fever","mesh","D015004"
> "9682","yellow fever","umls","C0043395"
> "9682","yellow fever","mondo","0020502"
> "0110119","autoimmune lymphoproliferative syndrome type 3","icd10cm","D47.9"
> "0110119","autoimmune lymphoproliferative syndrome type 3","mondo","0014253"
> "0110118","Leber congenital amaurosis 16","icd10cm","H35.5"
> "0110118","Leber congenital amaurosis 16","mondo","0013613"
> "0110117","autoimmune lymphoproliferative syndrome type 4","icd10cm","D72.8"
> "0110117","autoimmune lymphoproliferative syndrome type 4","mondo","0013767"
> "0110116","autoimmune lymphoproliferative syndrome type 2B","icd10cm","D47.9"
> "0110116","autoimmune lymphoproliferative syndrome type 2B","mondo","0011804"
> "0110115","autoimmune lymphoproliferative syndrome type 2A","icd10cm","D47.9"
> "0110115","autoimmune lymphoproliferative syndrome type 2A","mondo","0011383"
> "0110114","atrial heart septal defect 9","icd10cm","Q21.1"
> "0110114","atrial heart septal defect 9","mondo","0013770"
> "0110113","atrial heart septal defect 8","icd10cm","Q21.1"
> "0110113","atrial heart septal defect 8","mondo","0013750"
> "0110112","atrial heart septal defect 7","icd10cm","Q21.1"
> "0110112","atrial heart septal defect 7","mondo","0007173"
> "0110111","atrial heart septal defect 6","icd10cm","Q21.1"
> "0110111","atrial heart septal defect 6","mondo","0013123"
> "0110110","atrial heart septal defect 5","icd10cm","Q21.1"
> "0110110","atrial heart septal defect 5","mondo","0013011"
> "6854","ethmoid sinus ectopic meningioma","umls","C1333475"
> "6854","ethmoid sinus ectopic meningioma","mondo","0004014"
> "6857","pineal region mature teratoma","umls","C1335417"
> "6857","pineal region mature teratoma","mondo","0004016"
> "6856","pineal region teratoma","umls","C1335419"
> "6856","pineal region teratoma","mondo","0004015"
> "6858","pineal region immature teratoma","umls","C1335416"
> "6858","pineal region immature teratoma","mondo","0004017"
> "82","myotonic cataract","icd9cm","366.43"
> "82","myotonic cataract","umls","C0027128"
> "82","myotonic cataract","mondo","0004495"
> "83","cataract","icd10cm","H26"
> "83","cataract","icd9cm","366.8"
> "83","cataract","mesh","D002386"
> "83","cataract","umls","C0029531"
> "83","cataract","mondo","0005129"
> "84","osteochondritis dissecans","icd10cm","M93.2"
> "84","osteochondritis dissecans","icd10cm","M93.9"
> "84","osteochondritis dissecans","icd9cm","732.7"
> "84","osteochondritis dissecans","mesh","D010007"
> "84","osteochondritis dissecans","mesh","D010008"
> "84","osteochondritis dissecans","umls","C0029420"
> "84","osteochondritis dissecans","umls","C0029421"
> "84","osteochondritis dissecans","mondo","0017178"
> "0060413","chromosome 22q11.2 deletion syndrome, distal","mondo","0012740"
> "14291","LEOPARD syndrome","mesh","D044542"
> "14291","LEOPARD syndrome","umls","C0175704"
> "14291","LEOPARD syndrome","mondo","0007893"
> "8805","intermediate coronary syndrome","icd10cm","I20.0"
> "8805","intermediate coronary syndrome","icd9cm","411.1"
> "8805","intermediate coronary syndrome","mesh","D000789"
> "8805","intermediate coronary syndrome","umls","C0002965"
> "8805","intermediate coronary syndrome","mondo","0006805"
> "14292","vulvar dystrophy","icd10cm","N90.4"
> "14292","vulvar dystrophy","icd9cm","624.0"
> "14292","vulvar dystrophy","umls","C0013426"
> "14292","vulvar dystrophy","mondo","0001938"
> "8800","lung carcinoma in situ","icd10cm","D02.2"
> "8800","lung carcinoma in situ","icd9cm","231.2"
> "8800","lung carcinoma in situ","umls","C0154071"
> "8800","lung carcinoma in situ","mondo","0004660"
> "8802","trachea carcinoma in situ","icd10cm","D02.1"
> "8802","trachea carcinoma in situ","icd9cm","231.1"
> "8802","trachea carcinoma in situ","umls","C0154070"
> "8802","trachea carcinoma in situ","mondo","0004661"
> "6581","breast apocrine carcinoma","umls","C1332316"
> "6581","breast apocrine carcinoma","mondo","0003934"
> "6587","invasive tubular breast carcinoma","umls","C1328544"
> "6587","invasive tubular breast carcinoma","mondo","0003936"
> "6585","oncocytic breast carcinoma","umls","C1518574"
> "6585","oncocytic breast carcinoma","mondo","0003935"
> "8207","hilar lung carcinoma","umls","C1334445"
> "8207","hilar lung carcinoma","mondo","0004499"
> "8757","gastric mucosal hypertrophy","icd10cm","K29.6"
> "8757","gastric mucosal hypertrophy","icd9cm","535.2"
> "8757","gastric mucosal hypertrophy","mesh","D005758"
> "8757","gastric mucosal hypertrophy","umls","C0017155"
> "8757","gastric mucosal hypertrophy","mondo","0007652"
> "8203","sacral spinal canal and spinal cord meningioma","umls","C1335893"
> "8203","sacral spinal canal and spinal cord meningioma","mondo","0004498"
> "8200","tertiary syphilis","icd10cm","A52"
> "8200","tertiary syphilis","icd10cm","A52.3"
> "8200","tertiary syphilis","icd10cm","A52.9"
> "8200","tertiary syphilis","icd9cm","097.0"
> "8200","tertiary syphilis","mesh","C536774"
> "8200","tertiary syphilis","umls","C0153188"
> "8200","tertiary syphilis","mondo","0004497"
> "13474","progressive peripheral pterygium","icd9cm","372.42"
> "13474","progressive peripheral pterygium","umls","C0155155"
> "13474","progressive peripheral pterygium","mondo","0001723"
> "0060578","Noonan syndrome 1","icd10cm","Q87.1"
> "0060578","Noonan syndrome 1","mondo","0008104"
> "0060575","3MC syndrome 1","mondo","0009770"
> "0060574","von Willebrand's disease 2","mesh","D056728"
> "0060574","von Willebrand's disease 2","umls","C1264040"
> "0060574","von Willebrand's disease 2","mondo","0013304"
> "0060577","3MC syndrome 3","mondo","0009554"
> "0060576","3MC syndrome 2","mondo","0009927"
> "0060571","Ritscher-Schinzel syndrome 1","mondo","0009073"
> "0060570","cardiac tuberculosis","mesh","D014381"
> "0060570","cardiac tuberculosis","mondo","0000813"
> "0060573","von Willebrand's disease 1","mesh","D056725"
> "0060573","von Willebrand's disease 1","umls","C1264039"
> "0060573","von Willebrand's disease 1","mondo","0008668"
> "0060572","Ritscher-Schinzel syndrome 2","mondo","0010499"
> "14701","propionic acidemia","icd10cm","E71.121"
> "14701","propionic acidemia","mesh","D056693"
> "14701","propionic acidemia","umls","C0268579"
> "14701","propionic acidemia","umls","C2717876"
> "14701","propionic acidemia","mondo","0011628"
> "9877","urethral gland abscess","icd10cm","N34.0"
> "9877","urethral gland abscess","icd9cm","597.0"
> "9877","urethral gland abscess","umls","C0156278"
> "9877","urethral gland abscess","mondo","0004909"
> "9870","galactosemia","icd10cm","E74.21"
> "9870","galactosemia","icd9cm","271.1"
> "9870","galactosemia","mesh","D005693"
> "9870","galactosemia","umls","C0016952"
> "9870","galactosemia","mondo","0018116"
> "11155","hypohidrosis","icd10cm","L74.4"
> "11155","hypohidrosis","mesh","D007007"
> "11155","hypohidrosis","umls","C0020620"
> "11155","hypohidrosis","mondo","0006560"
> "11156","anhidrosis","icd10cm","L74.4"
> "11156","anhidrosis","icd9cm","705.0"
> "11156","anhidrosis","mesh","D007007"
> "11156","anhidrosis","umls","C0003028"
> "11156","anhidrosis","mondo","0006527"
> "11151","cholecystolithiasis","mesh","D041761"
> "11151","cholecystolithiasis","umls","C0947622"
> "11151","cholecystolithiasis","mondo","0006698"
> "11153","miliaria rubra","icd10cm","L74.0"
> "11153","miliaria rubra","icd9cm","705.1"
> "11153","miliaria rubra","mesh","D008883"
> "11153","miliaria rubra","umls","C0162423"
> "11153","miliaria rubra","mondo","0006581"
> "656","adrenal adenoma","mondo","0003924"
> "657","adenoma","mesh","D000236"
> "657","adenoma","umls","C0001430"
> "657","adenoma","umls","C0334389"
> "657","adenoma","mondo","0004972"
> "654","overnutrition","mesh","D044343"
> "654","overnutrition","umls","C1257763"
> "654","overnutrition","mondo","0003916"
> "655","inherited metabolic disorder","mesh","D008661"
> "655","inherited metabolic disorder","umls","C0025521"
> "655","inherited metabolic disorder","mondo","0019052"
> "3089","granulomatous orchitis","umls","C0436545"
> "3089","granulomatous orchitis","mondo","0002509"
> "653","purine-pyrimidine metabolic disorder","icd10cm","E79.8"
> "653","purine-pyrimidine metabolic disorder","icd9cm","277.2"
> "653","purine-pyrimidine metabolic disorder","umls","C0029595"
> "653","purine-pyrimidine metabolic disorder","mondo","0019254"
> "3087","gingivitis","icd10cm","K05.0"
> "3087","gingivitis","icd10cm","K05.00"
> "3087","gingivitis","icd10cm","K05.1"
> "3087","gingivitis","icd10cm","K05.10"
> "3087","gingivitis","icd9cm","523.0"
> "3087","gingivitis","icd9cm","523.1"
> "3087","gingivitis","mesh","D005891"
> "3087","gingivitis","umls","C0008684"
> "3087","gingivitis","umls","C0017574"
> "3087","gingivitis","umls","C0155937"
> "3087","gingivitis","mondo","0002508"
> "3086","gingival overgrowth","icd10cm","K06.1"
> "3086","gingival overgrowth","mesh","D019214"
> "3086","gingival overgrowth","umls","C0376480"
> "3086","gingival overgrowth","mondo","0002507"
> "3081","cystic lymphangioma","mesh","D018191"
> "3081","cystic lymphangioma","umls","C0206620"
> "3081","cystic lymphangioma","mondo","0006719"
> "3083","chronic obstructive pulmonary disease","icd10cm","J44.9"
> "3083","chronic obstructive pulmonary disease","mesh","D029424"
> "3083","chronic obstructive pulmonary disease","umls","C0024117"
> "3083","chronic obstructive pulmonary disease","mondo","0005002"
> "3082","interstitial lung disease","icd10cm","J84.9"
> "3082","interstitial lung disease","mesh","D017563"
> "3082","interstitial lung disease","umls","C0206062"
> "3082","interstitial lung disease","mondo","0015925"
> "3369","Ewing sarcoma","mesh","C563168"
> "3369","Ewing sarcoma","mesh","D012512"
> "3369","Ewing sarcoma","mesh","D018241"
> "3369","Ewing sarcoma","umls","C0553580"
> "3369","Ewing sarcoma","umls","C0684337"
> "3369","Ewing sarcoma","umls","C0796547"
> "3369","Ewing sarcoma","umls","C0863029"
> "3369","Ewing sarcoma","umls","C0877849"
> "3369","Ewing sarcoma","umls","C1334408"
> "3369","Ewing sarcoma","mondo","0012817"
> "13401","angioid streaks","mesh","D000793"
> "13401","angioid streaks","umls","C0002982"
> "13401","angioid streaks","mondo","0011782"
> "2088","outlet dysfunction constipation","icd10cm","K59.02"
> "2088","outlet dysfunction constipation","icd9cm","564.02"
> "2088","outlet dysfunction constipation","umls","C0949134"
> "2088","outlet dysfunction constipation","mondo","0002202"
> "2089","constipation","icd10cm","K59.0"
> "2089","constipation","icd10cm","K59.00"
> "2089","constipation","icd9cm","564.0"
> "2089","constipation","icd9cm","564.00"
> "2089","constipation","mesh","D003248"
> "2089","constipation","umls","C0009806"
> "2089","constipation","mondo","0002203"
> "13809","familial combined hyperlipidemia","icd10cm","E78.4"
> "13809","familial combined hyperlipidemia","mesh","D006950"
> "13809","familial combined hyperlipidemia","umls","C0020474"
> "13809","familial combined hyperlipidemia","mondo","0001807"
> "13801","pharyngoconjunctival fever","icd9cm","077.2"
> "13801","pharyngoconjunctival fever","mesh","D000258"
> "13801","pharyngoconjunctival fever","umls","C0031351"
> "13801","pharyngoconjunctival fever","mondo","0005911"
> "13800","inclusion conjunctivitis","icd10cm","A74.0"
> "13800","inclusion conjunctivitis","icd9cm","077.0"
> "13800","inclusion conjunctivitis","mesh","D003235"
> "13800","inclusion conjunctivitis","umls","C0009770"
> "13800","inclusion conjunctivitis","mondo","0005808"
> "3883","Lynch syndrome","mesh","D003123"
> "3883","Lynch syndrome","umls","C0009405"
> "3883","Lynch syndrome","umls","C1333990"
> "3883","Lynch syndrome","mondo","0005835"
> "1884","viral hepatitis","mesh","D006524"
> "1884","viral hepatitis","umls","C0019194"
> "1884","viral hepatitis","mondo","0006011"
> "0110863","congenital stationary night blindness autosomal dominant 2","mondo","0008099"
> "11527","laryngostenosis","icd10cm","J38.6"
> "11527","laryngostenosis","icd9cm","478.74"
> "11527","laryngostenosis","mesh","D007829"
> "11527","laryngostenosis","umls","C0023075"
> "11527","laryngostenosis","mondo","0001305"
> "11520","benign hypertensive renal disease","icd9cm","403.1"
> "11520","benign hypertensive renal disease","icd9cm","403.10"
> "11520","benign hypertensive renal disease","umls","C0155596"
> "11520","benign hypertensive renal disease","mondo","0001304"
> "1883","hepatitis C","icd10cm","B19.2"
> "1883","hepatitis C","icd10cm","B19.20"
> "1883","hepatitis C","icd9cm","070.7"
> "1883","hepatitis C","mesh","D006526"
> "1883","hepatitis C","umls","C0019196"
> "1883","hepatitis C","mondo","0005231"
10307,10332d24548
< "0111083","Fanconi anemia complementation group D2","mondo","0009214"
< "4000","ovary transitional cell carcinoma","umls","C1335184"
< "4000","ovary transitional cell carcinoma","umls","C1335185"
< "4000","ovary transitional cell carcinoma","umls","C1518237"
< "4000","ovary transitional cell carcinoma","mondo","0006343"
< "4001","ovarian carcinoma","mesh","C538090"
< "4001","ovarian carcinoma","umls","C0677886"
< "4001","ovarian carcinoma","mondo","0005140"
< "6039","uveal melanoma","mesh","C536494"
< "6039","uveal melanoma","umls","C0220633"
< "6039","uveal melanoma","mondo","0006486"
< "4006","bladder urothelial carcinoma","umls","C0279680"
< "4006","bladder urothelial carcinoma","mondo","0005611"
< "4007","bladder carcinoma","umls","C0699885"
< "4007","bladder carcinoma","mondo","0004986"
< "8484","maple bark strippers' lung","icd10cm","J67.6"
< "8484","maple bark strippers' lung","icd9cm","495.6"
< "8484","maple bark strippers' lung","umls","C0155890"
< "8484","maple bark strippers' lung","mondo","0004584"
< "3973","thyroid medullary carcinoma","mesh","C536914"
< "3973","thyroid medullary carcinoma","umls","C0238462"
< "3973","thyroid medullary carcinoma","mondo","0015277"
< "321","tropical spastic paraparesis","icd10cm","G04.1"
< "321","tropical spastic paraparesis","mesh","D015493"
< "321","tropical spastic paraparesis","umls","C0030481"
< "321","tropical spastic paraparesis","mondo","0008039"
10337,10368d24552
< "13369","tinea manuum","icd10cm","B35.2"
< "13369","tinea manuum","icd9cm","110.2"
< "13369","tinea manuum","umls","C0153246"
< "13369","tinea manuum","mondo","0001699"
< "0110868","congenital stationary night blindness 1D","mondo","0013450"
< "0080068","Charcot-Marie-Tooth disease type 6","mondo","0019551"
< "3620","central nervous system cancer","icd10cm","C72.9"
< "3620","central nervous system cancer","mesh","D016543"
< "3620","central nervous system cancer","umls","C0085136"
< "3620","central nervous system cancer","umls","C0348374"
< "3620","central nervous system cancer","mondo","0002714"
< "0080067","Charcot-Marie-Tooth disease type 5","mondo","0010877"
< "3627","aortic aneurysm","icd10cm","I71.1"
< "3627","aortic aneurysm","icd10cm","I71.3"
< "3627","aortic aneurysm","icd10cm","I71.5"
< "3627","aortic aneurysm","icd10cm","I71.8"
< "3627","aortic aneurysm","icd10cm","I71.9"
< "3627","aortic aneurysm","icd9cm","441.1"
< "3627","aortic aneurysm","icd9cm","441.3"
< "3627","aortic aneurysm","icd9cm","441.5"
< "3627","aortic aneurysm","icd9cm","441.6"
< "3627","aortic aneurysm","mesh","D001014"
< "3627","aortic aneurysm","mesh","D001019"
< "3627","aortic aneurysm","umls","C0003486"
< "3627","aortic aneurysm","umls","C0265010"
< "3627","aortic aneurysm","umls","C0265012"
< "3627","aortic aneurysm","umls","C0741160"
< "3627","aortic aneurysm","umls","C1305122"
< "3627","aortic aneurysm","mondo","0005160"
< "0111160","camptodactyly-tall stature-scoliosis-hearing loss syndrome","mesh","C537975"
< "0111160","camptodactyly-tall stature-scoliosis-hearing loss syndrome","umls","C1864852"
< "0111160","camptodactyly-tall stature-scoliosis-hearing loss syndrome","mondo","0012504"
10372c24556
< "0111162","epidermal nevus","mondo","0008093"
---
> "0110932","nemaline myopathy 4","mondo","0012240"
10378,10380c24562
< "13622","campylobacteriosis","mesh","D002169"
< "13622","campylobacteriosis","umls","C0006818"
< "13622","campylobacteriosis","mondo","0005688"
---
> "0110936","nemaline myopathy 5","mondo","0011539"
10385,10392d24566
< "4719","bone giant cell sarcoma","umls","C0334552"
< "4719","bone giant cell sarcoma","mondo","0006287"
< "3073","brain glioblastoma multiforme","umls","C0349543"
< "3073","brain glioblastoma multiforme","mondo","0002501"
< "2870","endometrial adenocarcinoma","umls","C0279763"
< "2870","endometrial adenocarcinoma","umls","C1153706"
< "2870","endometrial adenocarcinoma","umls","C1336905"
< "2870","endometrial adenocarcinoma","mondo","0005461"
10394,10416c24568,24569
< "0050675","Birk-Barel syndrome","mesh","C567357"
< "0050675","Birk-Barel syndrome","mondo","0012856"
< "3717","gastric adenocarcinoma","umls","C0278701"
< "3717","gastric adenocarcinoma","mondo","0005036"
< "0050569","Seckel syndrome","icd10cm","Q87.1"
< "0050569","Seckel syndrome","mondo","0019342"
< "14701","propionic acidemia","icd10cm","E71.121"
< "14701","propionic acidemia","mesh","D056693"
< "14701","propionic acidemia","umls","C0268579"
< "14701","propionic acidemia","umls","C2717876"
< "14701","propionic acidemia","mondo","0011628"
< "3713","ovary adenocarcinoma","umls","C0948216"
< "3713","ovary adenocarcinoma","mondo","0002752"
< "0050674","congenital bile acid synthesis defect","icd10cm","K76.8"
< "0050674","congenital bile acid synthesis defect","mondo","0018841"
< "0050564","autosomal dominant nonsyndromic deafness","icd10cm","H90.3"
< "0050564","autosomal dominant nonsyndromic deafness","mondo","0019587"
< "0050566","X-linked nonsyndromic deafness","icd10cm","H90.3"
< "0050566","X-linked nonsyndromic deafness","mondo","0019586"
< "0050561","Lennox-Gastaut syndrome","mondo","0016532"
< "0050560","Walker-Warburg syndrome","mesh","D058494"
< "0050560","Walker-Warburg syndrome","mondo","0019523"
< "0050562","West syndrome","mondo","0018097"
---
> "0111180","French Canadian Leigh disease","icd10cm","G3L8"
> "0111180","French Canadian Leigh disease","umls","C1857355"
10430,10440c24583,24585
< "0050768","mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","icd10cm","E88.8"
< "0050768","mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","mondo","0011421"
< "4471","chromophobe renal cell carcinoma","mesh","D002292"
< "4471","chromophobe renal cell carcinoma","umls","C1266042"
< "4471","chromophobe renal cell carcinoma","mondo","0017885"
< "0050766","choreaacanthocytosis","mesh","D054546"
< "0050766","choreaacanthocytosis","umls","C0393576"
< "0050766","choreaacanthocytosis","mondo","0008695"
< "0050764","Armfield syndrome","icd10cm","Q87.8"
< "0050764","Armfield syndrome","mondo","0010284"
< "0050763","ARC syndrome","mondo","0017123"
---
> "0110851","rhizomelic chondrodysplasia punctata type 1","icd10cm","Q77.3"
> "0110851","rhizomelic chondrodysplasia punctata type 1","mondo","0008972"
> "0110865","congenital stationary night blindness 1B","mondo","0009758"
10443,10448c24588,24600
< "4908","anal carcinoma","mesh","D001005"
< "4908","anal carcinoma","umls","C0279637"
< "4908","anal carcinoma","mondo","0003199"
< "0070002","3-methylglutaconic aciduria type IX","mondo","0044724"
< "4679","breast mucoepidermoid carcinoma","umls","C1334813"
< "4679","breast mucoepidermoid carcinoma","mondo","0003087"
---
> "6004","aleukemic leukemia","umls","C0877858"
> "6004","aleukemic leukemia","mondo","0003730"
> "6003","aleukemic leukemia cutis","umls","C0887846"
> "6003","aleukemic leukemia cutis","mondo","0003729"
> "6000","congestive heart failure","icd10cm","I50"
> "6000","congestive heart failure","icd10cm","I50.9"
> "6000","congestive heart failure","icd9cm","428"
> "6000","congestive heart failure","icd9cm","428.0"
> "6000","congestive heart failure","icd9cm","428.9"
> "6000","congestive heart failure","mesh","D006333"
> "6000","congestive heart failure","umls","C0018801"
> "6000","congestive heart failure","umls","C0018802"
> "6000","congestive heart failure","mondo","0005009"
10451,10498c24603
< "0090143","brachyolmia-amelogenesis imperfecta syndrome","icd10cm","Q76.3"
< "0090143","brachyolmia-amelogenesis imperfecta syndrome","mondo","0011018"
< "0090142","cystathioninuria","icd10cm","E72.19"
< "0090142","cystathioninuria","mesh","C535408"
< "0090142","cystathioninuria","umls","C0220993"
< "0090142","cystathioninuria","umls","C0268616"
< "0090142","cystathioninuria","mondo","0009058"
< "0090141","cortisone reductase deficiency 1","mondo","0011503"
< "4674","androgen insensitivity syndrome","icd10cm","E34.5"
< "4674","androgen insensitivity syndrome","icd10cm","E34.50"
< "4674","androgen insensitivity syndrome","icd10cm","E34.51"
< "4674","androgen insensitivity syndrome","icd9cm","259.5"
< "4674","androgen insensitivity syndrome","icd9cm","259.51"
< "4674","androgen insensitivity syndrome","mesh","D013734"
< "4674","androgen insensitivity syndrome","umls","C0039585"
< "4674","androgen insensitivity syndrome","umls","C0936016"
< "4674","androgen insensitivity syndrome","mondo","0019154"
< "4905","pancreatic carcinoma","mesh","C562463"
< "4905","pancreatic carcinoma","umls","C0235974"
< "4905","pancreatic carcinoma","mondo","0005192"
< "0090145","dopamine beta-hydroxylase deficiency","mesh","C535600"
< "0090145","dopamine beta-hydroxylase deficiency","umls","C0342687"
< "0090145","dopamine beta-hydroxylase deficiency","mondo","0009123"
< "0090144","Donnai-Barrow syndrome","mesh","C536390"
< "0090144","Donnai-Barrow syndrome","umls","C1857277"
< "0090144","Donnai-Barrow syndrome","mondo","0009104"
< "7437","uterus perivascular epithelioid cell tumor","umls","C1519862"
< "7437","uterus perivascular epithelioid cell tumor","mondo","0004221"
< "0111079","birdshot chorioretinopathy","mesh","C537630"
< "0111079","birdshot chorioretinopathy","umls","C1853959"
< "0111079","birdshot chorioretinopathy","mondo","0011599"
< "0111078","tibial muscular dystrophy","mesh","D049310"
< "0111078","tibial muscular dystrophy","umls","C1838244"
< "0111078","tibial muscular dystrophy","mondo","0010870"
< "0111077","pyruvate kinase deficiency of red cells","mondo","0009950"
< "0111076","progressive familial heart block type IB","mondo","0011474"
< "0111075","progressive familial heart block type II","mondo","0007701"
< "0111074","progressive familial heart block type IA","mondo","0007240"
< "0111073","progressive familial heart block","mondo","0019490"
< "0111072","myostatin-related muscle hypertrophy","mesh","C536106"
< "0111072","myostatin-related muscle hypertrophy","umls","C2931112"
< "0111072","myostatin-related muscle hypertrophy","mondo","0013598"
< "11702","dysgammaglobulinemia","mesh","D004406"
< "11702","dysgammaglobulinemia","umls","C0013374"
< "11702","dysgammaglobulinemia","mondo","0001342"
< "0111070","congenital bile acid synthesis defect 3","mesh","C566340"
< "0111070","congenital bile acid synthesis defect 3","umls","C3151147"
< "0111070","congenital bile acid synthesis defect 3","mondo","0013439"
---
> "0110864","congenital stationary night blindness 1F","mondo","0014026"
10506a24612,24616
> "997","uterine inversion","icd10cm","N85.5"
> "997","uterine inversion","icd9cm","665.2"
> "997","uterine inversion","mesh","D019687"
> "997","uterine inversion","umls","C0162482"
> "997","uterine inversion","mondo","0004936"
10511,10512c24621,24632
< "7390","superior vena cava leiomyosarcoma","umls","C1336531"
< "7390","superior vena cava leiomyosarcoma","mondo","0004208"
---
> "9274","hyperlysinemia","icd10cm","E72.3"
> "9274","hyperlysinemia","mesh","D020167"
> "9274","hyperlysinemia","umls","C0268553"
> "9274","hyperlysinemia","mondo","0009388"
> "9275","tyrosinemia","icd10cm","E70.21"
> "9275","tyrosinemia","mesh","D020176"
> "9275","tyrosinemia","umls","C0268483"
> "9275","tyrosinemia","mondo","0004741"
> "9277","primary cerebellar degeneration","icd9cm","334.2"
> "9277","primary cerebellar degeneration","mesh","D013132"
> "9277","primary cerebellar degeneration","umls","C0033132"
> "9277","primary cerebellar degeneration","mondo","0004742"
10517,10523c24637,24650
< "2468","psychotic disorder","icd9cm","298.8"
< "2468","psychotic disorder","umls","C0029516"
< "2468","psychotic disorder","mondo","0005485"
< "0050592","asphyxiating thoracic dystrophy","icd10cm","Q77.2"
< "0050592","asphyxiating thoracic dystrophy","mondo","0018770"
< "5140","gallbladder leiomyoma","umls","C1333745"
< "5140","gallbladder leiomyoma","mondo","0003297"
---
> "9279","hyperhomocysteinemia","mesh","D020138"
> "9279","hyperhomocysteinemia","umls","C0598608"
> "9279","hyperhomocysteinemia","mondo","0004743"
> "10054","skin amelanotic melanoma","umls","C0349515"
> "10054","skin amelanotic melanoma","mondo","0005208"
> "999","hypereosinophilic syndrome","icd10cm","D72.1"
> "999","hypereosinophilic syndrome","icd9cm","288.3"
> "999","hypereosinophilic syndrome","mesh","D004802"
> "999","hypereosinophilic syndrome","umls","C0014457"
> "999","hypereosinophilic syndrome","mondo","0015691"
> "998","eosinophilia-myalgia syndrome","icd9cm","710.5"
> "998","eosinophilia-myalgia syndrome","mesh","D016603"
> "998","eosinophilia-myalgia syndrome","umls","C0085179"
> "998","eosinophilia-myalgia syndrome","mondo","0004941"
10532,10536c24659,24662
< "0080313","cleft palate-lateral synechia syndrome","icd10cm","Q87.8"
< "0080313","cleft palate-lateral synechia syndrome","mesh","C563047"
< "0080313","cleft palate-lateral synechia syndrome","umls","C0795898"
< "0080313","cleft palate-lateral synechia syndrome","mondo","0007337"
< "0080312","neurodevelopmental disorder with midbrain and hindbrain malformations","mondo","0056797"
---
> "0110584","autosomal dominant nonsyndromic deafness 6","icd10cm","H90.3"
> "0110584","autosomal dominant nonsyndromic deafness 6","mondo","0010963"
> "0110585","autosomal dominant nonsyndromic deafness 64","icd10cm","H90.3"
> "0110585","autosomal dominant nonsyndromic deafness 64","mondo","0013593"
10545,10618c24671,24716
< "0080319","X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia","mondo","0010455"
< "0110610","primary ciliary dyskinesia 34","mondo","0014909"
< "10699","paragonimiasis","icd10cm","B66.4"
< "10699","paragonimiasis","icd9cm","121.2"
< "10699","paragonimiasis","mesh","D010237"
< "10699","paragonimiasis","umls","C0030424"
< "10699","paragonimiasis","mondo","0005895"
< "0110612","primary ciliary dyskinesia 10","icd10cm","Q34.8"
< "0110612","primary ciliary dyskinesia 10","mondo","0012918"
< "0110613","primary ciliary dyskinesia 16","icd10cm","Q34.8"
< "0110613","primary ciliary dyskinesia 16","mondo","0013525"
< "0110614","primary ciliary dyskinesia 4","icd10cm","Q34.8"
< "0110614","primary ciliary dyskinesia 4","mondo","0012087"
< "0110615","primary ciliary dyskinesia 25","icd10cm","Q34.8"
< "0110615","primary ciliary dyskinesia 25","mondo","0014203"
< "0110616","primary ciliary dyskinesia 8","icd10cm","Q34.8"
< "0110616","primary ciliary dyskinesia 8","mondo","0012844"
< "0110617","primary ciliary dyskinesia 5","icd10cm","Q34.8"
< "0110617","primary ciliary dyskinesia 5","mondo","0012088"
< "0110618","primary ciliary dyskinesia 13","icd10cm","Q34.8"
< "0110618","primary ciliary dyskinesia 13","mondo","0013174"
< "0110619","primary ciliary dyskinesia 33","icd10cm","Q34.8"
< "0110619","primary ciliary dyskinesia 33","mondo","0014750"
< "4879","Bartholin's gland adenoid cystic carcinoma","umls","C1511047"
< "4879","Bartholin's gland adenoid cystic carcinoma","mondo","0003187"
< "4878","esophageal adenoid cystic carcinoma","umls","C1333441"
< "4878","esophageal adenoid cystic carcinoma","mondo","0003186"
< "6312","clivus chordoma","umls","C1333071"
< "6312","clivus chordoma","mondo","0003849"
< "6313","clivus chondroid chordoma","umls","C1333072"
< "6313","clivus chondroid chordoma","mondo","0003850"
< "2799","bronchiolitis obliterans","mesh","D001989"
< "2799","bronchiolitis obliterans","umls","C0006272"
< "2799","bronchiolitis obliterans","mondo","0015265"
< "10615","acute gonococcal cervicitis","icd9cm","098.15"
< "10615","acute gonococcal cervicitis","umls","C0153195"
< "10615","acute gonococcal cervicitis","mondo","0001080"
< "0110951","Waardenburg syndrome type 2C","mondo","0011697"
< "0110441","dilated cardiomyopathy 2B","icd10cm","I42.0"
< "0110441","dilated cardiomyopathy 2B","mondo","0013848"
< "10619","lymph node cancer","umls","C0596869"
< "10619","lymph node cancer","mondo","0001082"
< "137","vaginal squamous papilloma","umls","C1336943"
< "137","vaginal squamous papilloma","mondo","0001779"
< "361","cervix endometriosis","umls","C0269107"
< "361","cervix endometriosis","mondo","0002706"
< "2797","idiopathic interstitial pneumonia","icd10cm","J84.11"
< "2797","idiopathic interstitial pneumonia","icd10cm","J84.112"
< "2797","idiopathic interstitial pneumonia","icd10cm","J84.114"
< "2797","idiopathic interstitial pneumonia","mesh","D011658"
< "2797","idiopathic interstitial pneumonia","umls","C0085786"
< "2797","idiopathic interstitial pneumonia","mondo","0002429"
< "2066","vulvar angiokeratoma","umls","C1274281"
< "2066","vulvar angiokeratoma","mondo","0002192"
< "0110596","primary ciliary dyskinesia 21","icd10cm","Q34.8"
< "0110596","primary ciliary dyskinesia 21","mondo","0014123"
< "0110038","Alzheimer's disease 6","icd10cm","G30"
< "0110038","Alzheimer's disease 6","mondo","0011561"
< "0110039","Alzheimer's disease 7","icd10cm","G30"
< "0110039","Alzheimer's disease 7","mondo","0011647"
< "14110","anus cancer","icd10cm","C21.0"
< "14110","anus cancer","icd10cm","C21.1"
< "14110","anus cancer","icd9cm","154.2"
< "14110","anus cancer","icd9cm","154.3"
< "14110","anus cancer","umls","C0153445"
< "14110","anus cancer","umls","C0153446"
< "14110","anus cancer","mondo","0001879"
< "14115","toxic shock syndrome","icd10cm","A48.3"
< "14115","toxic shock syndrome","icd9cm","040.82"
< "14115","toxic shock syndrome","mesh","D012772"
< "14115","toxic shock syndrome","umls","C0600327"
< "14115","toxic shock syndrome","mondo","0001881"
< "0110030","alpha thalassemia-X-linked intellectual disability syndrome","icd10cm","D56.0"
< "0110030","alpha thalassemia-X-linked intellectual disability syndrome","mondo","0010519"
---
> "0080087","nonsyndromic congenital nail disorder 9","mondo","0013592"
> "0080086","nonsyndromic congenital nail disorder 8","mondo","0011852"
> "0080085","nonsyndromic congenital nail disorder 7","mondo","0011595"
> "0080084","nonsyndromic congenital nail disorder 6","mondo","0007135"
> "0080083","nonsyndromic congenital nail disorder 5","mondo","0008125"
> "0080082","nonsyndromic congenital nail disorder 4","mesh","C536377"
> "0080082","nonsyndromic congenital nail disorder 4","mondo","0008798"
> "0080081","nonsyndromic congenital nail disorder 3","mondo","0007900"
> "0080080","nonsyndromic congenital nail disorder 2","mondo","0007867"
> "12385","shigellosis","kegg","05131"
> "12385","shigellosis","icd10cm","A03"
> "12385","shigellosis","icd10cm","A03.0"
> "12385","shigellosis","icd10cm","A03.1"
> "12385","shigellosis","icd10cm","A03.2"
> "12385","shigellosis","icd10cm","A03.9"
> "12385","shigellosis","icd9cm","004"
> "12385","shigellosis","icd9cm","004.0"
> "12385","shigellosis","icd9cm","004.1"
> "12385","shigellosis","icd9cm","004.2"
> "12385","shigellosis","icd9cm","004.9"
> "12385","shigellosis","mesh","D004405"
> "12385","shigellosis","umls","C0013371"
> "12385","shigellosis","umls","C0302358"
> "12385","shigellosis","umls","C0302359"
> "12385","shigellosis","umls","C0302360"
> "12385","shigellosis","mondo","0019345"
> "12384","dysentery","icd9cm","009.2"
> "12384","dysentery","mesh","D004403"
> "12384","dysentery","umls","C0013369"
> "12384","dysentery","mondo","0001517"
> "12387","nephrogenic diabetes insipidus","icd10cm","N25.1"
> "12387","nephrogenic diabetes insipidus","icd9cm","588.1"
> "12387","nephrogenic diabetes insipidus","mesh","D018500"
> "12387","nephrogenic diabetes insipidus","umls","C0162283"
> "12387","nephrogenic diabetes insipidus","mondo","0016383"
> "12386","balantidiasis","icd10cm","A07.0"
> "12386","balantidiasis","icd9cm","007.0"
> "12386","balantidiasis","mesh","D001447"
> "12386","balantidiasis","umls","C0004692"
> "12386","balantidiasis","mondo","0005662"
> "0080089","tubular aggregate myopathy","mondo","0008051"
> "0080088","nonsyndromic congenital nail disorder 10","mondo","0013596"
> "9098","sebaceous gland disease","icd10cm","L70.8"
> "9098","sebaceous gland disease","icd9cm","706.1"
> "9098","sebaceous gland disease","umls","C0029485"
> "9098","sebaceous gland disease","mondo","0006607"
10623,10643c24721,24730
< "14118","familial lipoprotein lipase deficiency","icd10cm","E78.3"
< "14118","familial lipoprotein lipase deficiency","icd9cm","272.3"
< "14118","familial lipoprotein lipase deficiency","mesh","D008072"
< "14118","familial lipoprotein lipase deficiency","umls","C0023817"
< "14118","familial lipoprotein lipase deficiency","mondo","0009387"
< "0110034","X-linked Alport syndrome","mondo","0010520"
< "0110035","Alzheimer's disease 2","icd10cm","G30"
< "0110035","Alzheimer's disease 2","mondo","0007089"
< "0110036","Alzheimer's disease 16","mondo","0010422"
< "0110037","Alzheimer's disease 5","icd10cm","G30"
< "0110037","Alzheimer's disease 5","mondo","0011194"
< "11990","ulceroglandular tularemia","icd10cm","A21.0"
< "11990","ulceroglandular tularemia","icd9cm","021.0"
< "11990","ulceroglandular tularemia","umls","C0152941"
< "11990","ulceroglandular tularemia","mondo","0001413"
< "0070127","congenital nongoitrous hypothyroidism 3","icd10cm","E03.1"
< "0070127","congenital nongoitrous hypothyroidism 3","mondo","0012360"
< "10128","venous insufficiency","icd9cm","459.81"
< "10128","venous insufficiency","mesh","D014689"
< "10128","venous insufficiency","umls","C0042485"
< "10128","venous insufficiency","mondo","0000945"
---
> "9097","erythematosquamous dermatosis","icd9cm","690"
> "9097","erythematosquamous dermatosis","umls","C0014747"
> "9097","erythematosquamous dermatosis","mondo","0006546"
> "9091","REM sleep behavior disorder","icd10cm","G47.52"
> "9091","REM sleep behavior disorder","icd9cm","327.42"
> "9091","REM sleep behavior disorder","mesh","D020187"
> "9091","REM sleep behavior disorder","umls","C0751772"
> "9091","REM sleep behavior disorder","mondo","0005937"
> "0050616","malignant Leydig cell tumor","umls","C0334410"
> "0050616","malignant Leydig cell tumor","mondo","0000377"
10649,10672c24736,24757
< "10690","mastitis","mesh","D008413"
< "10690","mastitis","umls","C0024894"
< "10690","mastitis","mondo","0006849"
< "0040031","diclofenac allergy","umls","C0570540"
< "0040036","tubocurarine allergy","umls","C0571147"
< "10126","keratoconus","icd10cm","H18.6"
< "10126","keratoconus","icd10cm","H18.60"
< "10126","keratoconus","icd9cm","371.6"
< "10126","keratoconus","icd9cm","371.60"
< "10126","keratoconus","mesh","D007640"
< "10126","keratoconus","umls","C0022578"
< "10126","keratoconus","mondo","0015486"
< "0040034","rocuronium allergy","umls","C0571149"
< "0070181","spermatogenic failure 23","mondo","0054727"
< "0070180","spermatogenic failure 11","mondo","0014037"
< "0070183","spermatogenic failure 5","umls","C0403812"
< "0070183","spermatogenic failure 5","mondo","0009461"
< "0070182","spermatogenic failure 13","mondo","0014365"
< "0070185","X-linked spermatogenic failure 2","mondo","0010647"
< "0070184","spermatogenic failure 16","mondo","0014961"
< "0070187","Y-linked spermatogenic failure 2","mondo","0010767"
< "0070186","Y-linked spermatogenic failure 1","mondo","0010763"
< "0070189","X-linked spermatogenic failure 1","mondo","0056795"
< "0070188","spermatogenic failure 1","mondo","0009776"
---
> "0050619","paranasal sinus cancer","mesh","D010255"
> "0050619","paranasal sinus cancer","umls","C0280334"
> "0050619","paranasal sinus cancer","umls","C0854995"
> "0050619","paranasal sinus cancer","umls","C1335336"
> "0050619","paranasal sinus cancer","umls","C1335337"
> "0050619","paranasal sinus cancer","umls","C1335340"
> "0050619","paranasal sinus cancer","mondo","0000380"
> "5099","middle ear cancer","umls","C0345617"
> "5099","middle ear cancer","mondo","0003275"
> "3579","testicular gonadoblastoma","umls","C1515283"
> "3579","testicular gonadoblastoma","mondo","0002698"
> "3578","ovarian gonadoblastoma","umls","C1518716"
> "3578","ovarian gonadoblastoma","mondo","0002697"
> "5090","sternum cancer","umls","C1290244"
> "5090","sternum cancer","umls","C1382025"
> "5090","sternum cancer","mondo","0003273"
> "3574","lateral sinus thrombosis","mesh","D020227"
> "3574","lateral sinus thrombosis","umls","C0270639"
> "3574","lateral sinus thrombosis","mondo","0002693"
> "3577","Sertoli cell tumor","mesh","D012707"
> "3577","Sertoli cell tumor","umls","C0036769"
> "3577","Sertoli cell tumor","mondo","0002696"
10689,10697c24774,24795
< "0050588","muscular dystrophy-dystroglycanopathy","icd10cm","G71.2"
< "0050588","muscular dystrophy-dystroglycanopathy","mondo","0018276"
< "9784","trichinosis","icd10cm","B75"
< "9784","trichinosis","icd9cm","124"
< "9784","trichinosis","mesh","D014235"
< "9784","trichinosis","umls","C0040896"
< "9784","trichinosis","mondo","0005992"
< "0110109","atrial heart septal defect 4","icd10cm","Q21.1"
< "0110109","atrial heart septal defect 4","mondo","0012654"
---
> "3572","intracranial sinus thrombosis","mesh","D012851"
> "3572","intracranial sinus thrombosis","umls","C0037198"
> "3572","intracranial sinus thrombosis","mondo","0002692"
> "13386","gastrointestinal anthrax","icd10cm","A22.2"
> "13386","gastrointestinal anthrax","icd9cm","022.2"
> "13386","gastrointestinal anthrax","mesh","C571911"
> "13386","gastrointestinal anthrax","umls","C0152945"
> "13386","gastrointestinal anthrax","mondo","0001701"
> "2667","benign mesenchymoma","umls","C0334491"
> "2667","benign mesenchymoma","mondo","0002382"
> "2664","sweat gland neoplasm","mesh","D013544"
> "2664","sweat gland neoplasm","umls","C0038987"
> "2664","sweat gland neoplasm","mondo","0002381"
> "0110860","polycystic kidney disease 3","mondo","0010916"
> "13382","megaloblastic anemia","icd10cm","D53.1"
> "13382","megaloblastic anemia","mesh","D000749"
> "13382","megaloblastic anemia","umls","C0002888"
> "13382","megaloblastic anemia","mondo","0001700"
> "4492","avian influenza","icd10cm","J09.X"
> "4492","avian influenza","mesh","D005585"
> "4492","avian influenza","umls","C0016627"
> "4492","avian influenza","mondo","0018695"
10704,10714c24802,24808
< "0110104","atopic dermatitis 8","mondo","0013294"
< "0110105","atopic dermatitis 9","mondo","0013295"
< "0110106","atrial heart septal defect 1","icd10cm","Q21.1"
< "0110106","atrial heart septal defect 1","mondo","0007172"
< "0110107","atrial heart septal defect 2","icd10cm","Q21.1"
< "0110107","atrial heart septal defect 2","mondo","0011938"
< "0110100","atopic dermatitis 4","mondo","0011598"
< "0110101","atopic dermatitis 5","mondo","0011608"
< "0110102","atopic dermatitis 6","mondo","0011609"
< "13389","labia majora carcinoma","umls","C1334356"
< "13389","labia majora carcinoma","mondo","0001702"
---
> "0111459","classic galactosemia","umls","C0268151"
> "0111458","galactose epimerase deficiency","umls","C0751161"
> "2668","mesenchymoma","mesh","D008637"
> "2668","mesenchymoma","umls","C0025464"
> "2668","mesenchymoma","mondo","0006854"
> "2669","Pacinian tumor","umls","C0334599"
> "2669","Pacinian tumor","mondo","0002383"
10716,10717d24809
< "0110603","primary ciliary dyskinesia 32","icd10cm","Q34.8"
< "0110603","primary ciliary dyskinesia 32","mondo","0014657"
10734a24827,24834
> "5327","retinal detachment","icd10cm","H33.2"
> "5327","retinal detachment","icd9cm","361.9"
> "5327","retinal detachment","mesh","D012163"
> "5327","retinal detachment","umls","C0035305"
> "5327","retinal detachment","mondo","0008375"
> "5324","fallopian tube germ cell cancer","umls","C1517114"
> "5324","fallopian tube germ cell cancer","mondo","0003392"
> "0050809","mucopolysaccharidosis IX","mondo","0011093"
10738,10739c24838
< "4524","prostate angiosarcoma","umls","C1335504"
< "4524","prostate angiosarcoma","mondo","0003033"
---
> "0050800","creatine transporter deficiency","mondo","0010305"
10741,10760c24840,24855
< "12375","bronchopneumonia","icd10cm","J18.0"
< "12375","bronchopneumonia","icd9cm","485"
< "12375","bronchopneumonia","mesh","D001996"
< "12375","bronchopneumonia","umls","C0006285"
< "12375","bronchopneumonia","mondo","0005682"
< "1647","female breast upper-inner quadrant cancer","icd9cm","174.2"
< "1647","female breast upper-inner quadrant cancer","umls","C0153550"
< "1647","female breast upper-inner quadrant cancer","mondo","0002067"
< "1641","benign breast adenomyoepithelioma","umls","C1332477"
< "1641","benign breast adenomyoepithelioma","mondo","0002065"
< "1642","breast adenomyoepithelioma","umls","C1334564"
< "1642","breast adenomyoepithelioma","umls","C1510795"
< "1642","breast adenomyoepithelioma","mondo","0002066"
< "1649","female breast lower-inner quadrant cancer","icd10cm","C50.31"
< "1649","female breast lower-inner quadrant cancer","icd9cm","174.3"
< "1649","female breast lower-inner quadrant cancer","umls","C0153551"
< "1649","female breast lower-inner quadrant cancer","mondo","0002068"
< "0070080","schizophrenia 4","mondo","0010943"
< "0110163","Charcot-Marie-Tooth disease axonal type 2F","icd10cm","G60.0"
< "0110163","Charcot-Marie-Tooth disease axonal type 2F","mondo","0011687"
---
> "0050807","Kahrizi syndrome","mondo","0012991"
> "1837","diabetic ketoacidosis","icd9cm","250.1"
> "1837","diabetic ketoacidosis","mesh","D016883"
> "1837","diabetic ketoacidosis","umls","C0011880"
> "1837","diabetic ketoacidosis","mondo","0012819"
> "13038","cicatricial lagophthalmos","icd10cm","H02.21"
> "13038","cicatricial lagophthalmos","icd9cm","374.23"
> "13038","cicatricial lagophthalmos","umls","C0155199"
> "13038","cicatricial lagophthalmos","mondo","0001623"
> "13034","relapsing fever","icd10cm","A68"
> "13034","relapsing fever","icd10cm","A68.9"
> "13034","relapsing fever","icd9cm","087"
> "13034","relapsing fever","icd9cm","087.9"
> "13034","relapsing fever","mesh","D012061"
> "13034","relapsing fever","umls","C0035021"
> "13034","relapsing fever","mondo","0019633"
10769,10787c24864,24879
< "14289","Ebstein anomaly","icd10cm","Q22.5"
< "14289","Ebstein anomaly","icd9cm","746.2"
< "14289","Ebstein anomaly","mesh","D004437"
< "14289","Ebstein anomaly","umls","C0013481"
< "14289","Ebstein anomaly","mondo","0009144"
< "0070082","schizophrenia 6","mondo","0011280"
< "0110970","brachydactyly type C","mesh","C537093"
< "0110970","brachydactyly type C","umls","C1300268"
< "0110970","brachydactyly type C","umls","C1862103"
< "0110970","brachydactyly type C","mondo","0007221"
< "0070083","schizophrenia 7","mondo","0011295"
< "1270","hereditary hemorrhagic telangiectasia","icd10cm","I78.0"
< "1270","hereditary hemorrhagic telangiectasia","icd9cm","448.0"
< "1270","hereditary hemorrhagic telangiectasia","mesh","D013683"
< "1270","hereditary hemorrhagic telangiectasia","umls","C0039445"
< "1270","hereditary hemorrhagic telangiectasia","mondo","0019180"
< "0060439","lysinuric protein intolerance","mesh","C562687"
< "0060439","lysinuric protein intolerance","umls","C0268647"
< "0060439","lysinuric protein intolerance","mondo","0009109"
---
> "13037","mechanical lagophthalmos","icd10cm","H02.22"
> "13037","mechanical lagophthalmos","icd9cm","374.22"
> "13037","mechanical lagophthalmos","umls","C0155198"
> "13037","mechanical lagophthalmos","mondo","0001622"
> "13031","balanoposthitis","icd10cm","N47.6"
> "13031","balanoposthitis","icd9cm","607.1"
> "13031","balanoposthitis","umls","C0004691"
> "13031","balanoposthitis","mondo","0001618"
> "13033","balanitis","icd10cm","N48.1"
> "13033","balanitis","mesh","D001446"
> "13033","balanitis","umls","C0004690"
> "13033","balanitis","mondo","0006672"
> "0060298","complement component 4b deficiency","icd10cm","D84.1"
> "0060298","complement component 4b deficiency","mondo","0013720"
> "0060299","complement component 6 deficiency","icd10cm","D84.1"
> "0060299","complement component 6 deficiency","mondo","0012908"
10796a24889,24890
> "0060293","autosomal dominant chondrodysplasia punctata","icd10cm","Q77.3"
> "0060293","autosomal dominant chondrodysplasia punctata","mondo","0007321"
10800,10812c24894,24900
< "8741","seborrheic dermatitis","icd10cm","L21"
< "8741","seborrheic dermatitis","icd10cm","L21.9"
< "8741","seborrheic dermatitis","icd9cm","690.1"
< "8741","seborrheic dermatitis","icd9cm","690.10"
< "8741","seborrheic dermatitis","icd9cm","706.3"
< "8741","seborrheic dermatitis","mesh","D012628"
< "8741","seborrheic dermatitis","umls","C0036508"
< "8741","seborrheic dermatitis","mondo","0006608"
< "13534","purulent labyrinthitis","icd9cm","386.33"
< "13534","purulent labyrinthitis","umls","C0155506"
< "13534","purulent labyrinthitis","mondo","0001739"
< "12969","central nervous system leukemia","umls","C1332884"
< "12969","central nervous system leukemia","mondo","0001606"
---
> "0060295","complement component 2 deficiency","icd10cm","D84.1"
> "0060295","complement component 2 deficiency","mondo","0009006"
> "0060296","congenital secretory chloride diarrhea 1","mesh","C536210"
> "0060296","congenital secretory chloride diarrhea 1","umls","C0267662"
> "0060296","congenital secretory chloride diarrhea 1","mondo","0008964"
> "0060297","complement component 4a deficiency","icd10cm","D84.1"
> "0060297","complement component 4a deficiency","mondo","0013721"
10816,10821c24904,24910
< "2800","acute interstitial pneumonia","icd10cm","J84.114"
< "2800","acute interstitial pneumonia","icd9cm","516.33"
< "2800","acute interstitial pneumonia","umls","C1279945"
< "2800","acute interstitial pneumonia","mondo","0019203"
< "2801","nonspecific interstitial pneumonia","umls","C1290344"
< "2801","nonspecific interstitial pneumonia","mondo","0019622"
---
> "3166","obsolete leukemoid reaction","icd10cm","D72.823"
> "3166","obsolete leukemoid reaction","icd9cm","288.62"
> "3166","obsolete leukemoid reaction","mesh","D007955"
> "3166","obsolete leukemoid reaction","umls","C0023501"
> "3165","skin benign neoplasm","mesh","D012878"
> "3165","skin benign neoplasm","umls","C0037286"
> "3165","skin benign neoplasm","mondo","0002531"
10824,10866d24912
< "12960","acrocephalosyndactylia","icd9cm","755.55"
< "12960","acrocephalosyndactylia","mesh","D000168"
< "12960","acrocephalosyndactylia","umls","C1510455"
< "12960","acrocephalosyndactylia","mondo","0019796"
< "1025","tuberculoid leprosy","icd10cm","A30.1"
< "1025","tuberculoid leprosy","icd9cm","030.1"
< "1025","tuberculoid leprosy","mesh","D015441"
< "1025","tuberculoid leprosy","umls","C0023351"
< "1025","tuberculoid leprosy","mondo","0005126"
< "0060569","hypertrichotic osteochondrodysplasia Cantu type","mesh","C535572"
< "0060569","hypertrichotic osteochondrodysplasia Cantu type","mondo","0009406"
< "3368","bone Ewing's sarcoma","umls","C0585474"
< "3368","bone Ewing's sarcoma","umls","C1333481"
< "3368","bone Ewing's sarcoma","umls","C1334406"
< "3368","bone Ewing's sarcoma","mondo","0002625"
< "3369","Ewing sarcoma","mesh","C563168"
< "3369","Ewing sarcoma","mesh","D012512"
< "3369","Ewing sarcoma","mesh","D018241"
< "3369","Ewing sarcoma","umls","C0553580"
< "3369","Ewing sarcoma","umls","C0684337"
< "3369","Ewing sarcoma","umls","C0796547"
< "3369","Ewing sarcoma","umls","C0863029"
< "3369","Ewing sarcoma","umls","C0877849"
< "3369","Ewing sarcoma","umls","C1334408"
< "3369","Ewing sarcoma","mondo","0012817"
< "0060562","anomalous left coronary artery from the pulmonary artery","mesh","D063748"
< "0060562","anomalous left coronary artery from the pulmonary artery","mondo","0000811"
< "0060560","lethal congenital contracture syndrome 2","mesh","C564369"
< "0060560","lethal congenital contracture syndrome 2","mondo","0011868"
< "4249","Gerstmann-Straussler-Scheinker syndrome","icd10cm","A81.82"
< "4249","Gerstmann-Straussler-Scheinker syndrome","icd9cm","046.71"
< "4249","Gerstmann-Straussler-Scheinker syndrome","mesh","D016098"
< "4249","Gerstmann-Straussler-Scheinker syndrome","umls","C0017495"
< "4249","Gerstmann-Straussler-Scheinker syndrome","mondo","0007656"
< "0060566","Holzgreve-Wagner-Rehder Syndrome","mesh","C535327"
< "0060566","Holzgreve-Wagner-Rehder Syndrome","umls","C1856095"
< "0060566","Holzgreve-Wagner-Rehder Syndrome","mondo","0009350"
< "14737","craniofrontonasal syndrome","mesh","C536456"
< "14737","craniofrontonasal syndrome","umls","C0220767"
< "14737","craniofrontonasal syndrome","mondo","0010570"
< "0060565","Ritscher-Schinzel syndrome","mesh","C535313"
< "0060565","Ritscher-Schinzel syndrome","umls","C0796137"
< "0060565","Ritscher-Schinzel syndrome","mondo","0019078"
10869a24916,24918
> "730","urethral benign neoplasm","mesh","D014523"
> "730","urethral benign neoplasm","umls","C0041971"
> "730","urethral benign neoplasm","mondo","0004177"
10874,10996c24923,24938
< "0060368","autosomal recessive juvenile Parkinson's disease 2","mondo","0010820"
< "0060369","autosomal recessive early-onset Parkinson's disease 6","mondo","0011613"
< "0060364","Galloway-Mowat syndrome","mesh","C537548"
< "0060364","Galloway-Mowat syndrome","umls","C0795949"
< "0060364","Galloway-Mowat syndrome","mondo","0009627"
< "0060365","mandibulofacial dysostosis with alopecia","mondo","0014608"
< "0060366","Hennekam syndrome","mesh","C537255"
< "0060366","Hennekam syndrome","umls","C0340834"
< "0060366","Hennekam syndrome","mondo","0016256"
< "6171","uterine carcinosarcoma","umls","C0280630"
< "6171","uterine carcinosarcoma","mondo","0006485"
< "0060361","punctate palmoplantar keratoderma","umls","C1274216"
< "0060361","punctate palmoplantar keratoderma","mondo","0017675"
< "0060362","punctate palmoplantar keratoderma type III","mesh","C535653"
< "0060362","punctate palmoplantar keratoderma type III","umls","C0545044"
< "0060362","punctate palmoplantar keratoderma type III","mondo","0007047"
< "0060584","Noonan syndrome 6","icd10cm","Q87.1"
< "0060584","Noonan syndrome 6","mondo","0013186"
< "0060585","Noonan syndrome 7","icd10cm","Q87.1"
< "0060585","Noonan syndrome 7","mondo","0013379"
< "4271","microsporidiosis","icd10cm","B60.8"
< "4271","microsporidiosis","mesh","D016881"
< "4271","microsporidiosis","umls","C0085407"
< "4271","microsporidiosis","mondo","0005846"
< "0060587","Noonan syndrome 9","icd10cm","Q87.1"
< "0060587","Noonan syndrome 9","mondo","0014691"
< "0060580","Noonan syndrome 2","icd10cm","Q87.1"
< "0060580","Noonan syndrome 2","mondo","0011531"
< "0060581","Noonan syndrome 3","icd10cm","Q87.1"
< "0060581","Noonan syndrome 3","mondo","0012371"
< "0060582","Noonan syndrome 4","icd10cm","Q87.1"
< "0060582","Noonan syndrome 4","mondo","0012547"
< "0060583","Noonan syndrome 5","icd10cm","Q87.1"
< "0060583","Noonan syndrome 5","mondo","0012690"
< "4279","infundibulocystic basal cell carcinoma","mondo","0011465"
< "2401","clitoris cancer","icd10cm","C51.2"
< "2401","clitoris cancer","icd9cm","184.3"
< "2401","clitoris cancer","umls","C0153589"
< "2401","clitoris cancer","umls","C1333070"
< "2401","clitoris cancer","mondo","0002290"
< "0060588","Noonan syndrome 10","icd10cm","Q87.1"
< "0060588","Noonan syndrome 10","mondo","0014693"
< "0060589","Yunis-Varon syndrome","mesh","C536719"
< "0060589","Yunis-Varon syndrome","umls","C1857663"
< "0060589","Yunis-Varon syndrome","mondo","0008995"
< "6284","epicardium lipoma","umls","C1333411"
< "6284","epicardium lipoma","mondo","0003840"
< "5557","testicular germ cell cancer","mesh","C563236"
< "5557","testicular germ cell cancer","umls","C1336708"
< "5557","testicular germ cell cancer","mondo","0010108"
< "5551","choriocarcinoma of the testis","umls","C0238449"
< "5551","choriocarcinoma of the testis","mondo","0003508"
< "5550","choriocarcinoma of ovary","umls","C0346181"
< "5550","choriocarcinoma of ovary","mondo","0003507"
< "12270","coloboma","icd10cm","Q13.0"
< "12270","coloboma","mesh","D003103"
< "12270","coloboma","umls","C0009363"
< "12270","coloboma","mondo","0001476"
< "9861","miliary tuberculosis","icd10cm","A19"
< "9861","miliary tuberculosis","icd10cm","A19.9"
< "9861","miliary tuberculosis","icd9cm","018"
< "9861","miliary tuberculosis","icd9cm","018.9"
< "9861","miliary tuberculosis","icd9cm","018.90"
< "9861","miliary tuberculosis","mesh","D014391"
< "9861","miliary tuberculosis","umls","C0041321"
< "9861","miliary tuberculosis","mondo","0005848"
< "5559","mediastinal cancer","icd10cm","C38.3"
< "5559","mediastinal cancer","icd9cm","164.9"
< "5559","mediastinal cancer","mesh","D008479"
< "5559","mediastinal cancer","umls","C0025063"
< "5559","mediastinal cancer","umls","C0153504"
< "5559","mediastinal cancer","mondo","0005843"
< "0110892","inflammatory bowel disease 1","mondo","0009960"
< "10744","broad ligament malignant neoplasm","icd10cm","C57.1"
< "10744","broad ligament malignant neoplasm","icd9cm","183.3"
< "10744","broad ligament malignant neoplasm","umls","C0346866"
< "10744","broad ligament malignant neoplasm","mondo","0001108"
< "14422","dipetalonemiasis","icd9cm","125.4"
< "14422","dipetalonemiasis","mesh","D004154"
< "14422","dipetalonemiasis","umls","C0012517"
< "14422","dipetalonemiasis","mondo","0005731"
< "9452","fatty liver disease","icd10cm","K70.0"
< "9452","fatty liver disease","icd9cm","571.0"
< "9452","fatty liver disease","mesh","D005234"
< "9452","fatty liver disease","mesh","D005235"
< "9452","fatty liver disease","umls","C0015695"
< "9452","fatty liver disease","umls","C0015696"
< "9452","fatty liver disease","mondo","0004790"
< "12275","cutaneous diphtheria","icd10cm","A36.3"
< "12275","cutaneous diphtheria","icd9cm","032.85"
< "12275","cutaneous diphtheria","umls","C0012555"
< "12275","cutaneous diphtheria","mondo","0001479"
< "0060468","Holt-Oram syndrome","icd10cm","Q87.2"
< "0060468","Holt-Oram syndrome","mesh","C535326"
< "0060468","Holt-Oram syndrome","umls","C0265264"
< "0060468","Holt-Oram syndrome","mondo","0007732"
< "4955","central nervous system melanocytic neoplasm","umls","C0349623"
< "4955","central nervous system melanocytic neoplasm","umls","C1332887"
< "4955","central nervous system melanocytic neoplasm","mondo","0003222"
< "1519","cecum carcinoma","umls","C0149640"
< "1519","cecum carcinoma","mondo","0006029"
< "1518","cecal disease","mesh","D002429"
< "1518","cecal disease","umls","C0007527"
< "1518","cecal disease","mondo","0002031"
< "5524","adenoid squamous cell carcinoma","umls","C0334250"
< "5524","adenoid squamous cell carcinoma","umls","C0334393"
< "5524","adenoid squamous cell carcinoma","mondo","0003487"
< "1517","cecal benign neoplasm","mesh","D002430"
< "1517","cecal benign neoplasm","umls","C0007528"
< "1517","cecal benign neoplasm","mondo","0005694"
< "0110763","hereditary spastic paraplegia 10","icd10cm","G11.4"
< "0110763","hereditary spastic paraplegia 10","mondo","0011408"
< "1510","personality disorder","icd9cm","301.8"
< "1510","personality disorder","icd9cm","301.89"
< "1510","personality disorder","umls","C0029707"
< "1510","personality disorder","mondo","0002028"
< "1512","chronic gonorrhea of cervix","icd9cm","098.35"
< "1512","chronic gonorrhea of cervix","umls","C0153206"
< "1512","chronic gonorrhea of cervix","mondo","0002029"
< "0060638","neonatal diabetes mellitus with congenital hypothyroidism","mondo","0012436"
< "0060639","permanent neonatal diabetes mellitus","mondo","0011643"
< "0110029","alpha thalassemia-intellectual disability syndrome type 1","icd10cm","D56.0"
< "0110029","alpha thalassemia-intellectual disability syndrome type 1","mondo","0007716"
---
> "734","urethra cancer","icd10cm","C68.0"
> "734","urethra cancer","icd9cm","189.3"
> "734","urethra cancer","mesh","D014523"
> "734","urethra cancer","umls","C0153620"
> "734","urethra cancer","umls","C0700101"
> "734","urethra cancer","mondo","0004192"
> "736","male urethral cancer","umls","C1518164"
> "736","male urethral cancer","mondo","0004197"
> "738","female urethral cancer","umls","C1517154"
> "738","female urethral cancer","mondo","0004203"
> "2153","ovarian Wilms' cancer","umls","C1518746"
> "2153","ovarian Wilms' cancer","mondo","0002230"
> "13742","neurofibroma of spinal cord","umls","C1336047"
> "13742","neurofibroma of spinal cord","mondo","0001789"
> "0110184","Charcot-Marie-Tooth disease type 4J","icd10cm","G60.0"
> "0110184","Charcot-Marie-Tooth disease type 4J","mondo","0012640"
11013,11024c24955,24964
< "0110539","autosomal recessive nonsyndromic deafness 97","icd10cm","H90.3"
< "0110539","autosomal recessive nonsyndromic deafness 97","mondo","0014739"
< "13819","lymphogranuloma venereum","icd10cm","A55"
< "13819","lymphogranuloma venereum","icd9cm","099.1"
< "13819","lymphogranuloma venereum","mesh","D008219"
< "13819","lymphogranuloma venereum","umls","C0024286"
< "13819","lymphogranuloma venereum","mondo","0005834"
< "5384","bile duct cystadenoma","umls","C0334285"
< "5384","bile duct cystadenoma","mondo","0003420"
< "0110890","inflammatory bowel disease 19","mondo","0012845"
< "13812","adhesions of uterus","umls","C0241593"
< "13812","adhesions of uterus","mondo","0001809"
---
> "8564","lip cancer","icd10cm","C00"
> "8564","lip cancer","icd10cm","C00.9"
> "8564","lip cancer","icd9cm","140"
> "8564","lip cancer","icd9cm","140.6"
> "8564","lip cancer","icd9cm","140.8"
> "8564","lip cancer","mesh","D008048"
> "8564","lip cancer","umls","C0153340"
> "8564","lip cancer","umls","C0153346"
> "8564","lip cancer","umls","C0153347"
> "8564","lip cancer","mondo","0006834"
11035,11039d24974
< "6554","ovarian clear cell malignant adenofibroma","mondo","0003922"
< "11838","penis sarcoma","umls","C0238352"
< "11838","penis sarcoma","mondo","0001387"
< "5387","middle ear adenoma","umls","C1334759"
< "5387","middle ear adenoma","mondo","0003423"
11042,11044c24977,24978
< "10286","prostate carcinoma","kegg","05215"
< "10286","prostate carcinoma","umls","C0600139"
< "10286","prostate carcinoma","mondo","0005159"
---
> "0060743","methylmalonic acidemia cblB type","icd10cm","E71.1"
> "0060743","methylmalonic acidemia cblB type","mondo","0009614"
11065,11075c24999,25001
< "6457","Cowden syndrome","mesh","D006223"
< "6457","Cowden syndrome","umls","C0018553"
< "6457","Cowden syndrome","umls","C0391826"
< "6457","Cowden syndrome","mondo","0016063"
< "10283","prostate cancer","kegg","05215"
< "10283","prostate cancer","icd10cm","C61"
< "10283","prostate cancer","icd9cm","185"
< "10283","prostate cancer","mesh","D011471"
< "10283","prostate cancer","umls","C0033578"
< "10283","prostate cancer","umls","C0376358"
< "10283","prostate cancer","mondo","0008315"
---
> "7475","diverticulitis","mesh","D004238"
> "7475","diverticulitis","umls","C0012813"
> "7475","diverticulitis","mondo","0004235"
11078,11089d25003
< "11555","Fuchs' endothelial dystrophy","icd10cm","H18.51"
< "11555","Fuchs' endothelial dystrophy","mesh","D005642"
< "11555","Fuchs' endothelial dystrophy","umls","C0016781"
< "11555","Fuchs' endothelial dystrophy","mondo","0005321"
< "11557","acute serous otitis media","icd10cm","H65.0"
< "11557","acute serous otitis media","icd10cm","H65.00"
< "11557","acute serous otitis media","icd9cm","381.01"
< "11557","acute serous otitis media","umls","C0155415"
< "11557","acute serous otitis media","mondo","0001312"
< "0060395","chromosome 15q24 deletion syndrome","icd10cm","Q93.5"
< "0060395","chromosome 15q24 deletion syndrome","mesh","C579849"
< "0060395","chromosome 15q24 deletion syndrome","mondo","0013256"
11098,11120c25012,25024
< "5386","lung adenoma","umls","C0345964"
< "5386","lung adenoma","mondo","0003422"
< "11394","adult respiratory distress syndrome","icd10cm","J80"
< "11394","adult respiratory distress syndrome","mesh","D012128"
< "11394","adult respiratory distress syndrome","umls","C0035222"
< "11394","adult respiratory distress syndrome","mondo","0006502"
< "4013","urethra transitional cell carcinoma","umls","C0863015"
< "4013","urethra transitional cell carcinoma","mondo","0002836"
< "4012","papillary transitional carcinoma","umls","C0334274"
< "4012","papillary transitional carcinoma","mondo","0002835"
< "4015","spindle cell carcinoma","mesh","D002277"
< "4015","spindle cell carcinoma","umls","C0205697"
< "4015","spindle cell carcinoma","mondo","0006406"
< "4014","sarcomatoid transitional cell carcinoma","umls","C0334271"
< "4014","sarcomatoid transitional cell carcinoma","mondo","0002837"
< "7503","extrahepatic bile duct papillary adenoma","umls","C1333510"
< "7503","extrahepatic bile duct papillary adenoma","mondo","0004250"
< "0040029","trimethoprim allergy","umls","C0571390"
< "0080195","Marinesco-Sjogren syndrome","mondo","0009567"
< "3983","oesophagostomiasis","mesh","D009814"
< "3983","oesophagostomiasis","umls","C0028887"
< "3983","oesophagostomiasis","mondo","0005880"
< "0080036","SOST-related sclerosing bone dysplasia","mondo","0009395"
---
> "14415","Legg-Calve-Perthes disease","icd10cm","M91.2"
> "14415","Legg-Calve-Perthes disease","icd10cm","M91.3"
> "14415","Legg-Calve-Perthes disease","mesh","D007873"
> "14415","Legg-Calve-Perthes disease","umls","C0022441"
> "14415","Legg-Calve-Perthes disease","umls","C0023234"
> "14415","Legg-Calve-Perthes disease","mondo","0007885"
> "3610","breast mucinous carcinoma","umls","C1334807"
> "3610","breast mucinous carcinoma","mondo","0002707"
> "14418","dracunculiasis","icd10cm","B72"
> "14418","dracunculiasis","icd9cm","125.7"
> "14418","dracunculiasis","mesh","D004320"
> "14418","dracunculiasis","umls","C0013100"
> "14418","dracunculiasis","mondo","0016472"
11122,11131c25026,25043
< "4877","breast adenoid cystic carcinoma","umls","C1332167"
< "4877","breast adenoid cystic carcinoma","mondo","0003185"
< "0110894","inflammatory bowel disease 11","mondo","0008617"
< "6128","gliomatosis cerebri","mesh","D018302"
< "6128","gliomatosis cerebri","umls","C0334576"
< "6128","gliomatosis cerebri","mondo","0016683"
< "13636","Fanconi anemia","icd10cm","D61.09"
< "13636","Fanconi anemia","mesh","D005199"
< "13636","Fanconi anemia","umls","C0015625"
< "13636","Fanconi anemia","mondo","0019391"
---
> "0050448","hereditary mucosal leukokeratosis","mesh","D053529"
> "0050448","hereditary mucosal leukokeratosis","umls","C1721005"
> "0050448","hereditary mucosal leukokeratosis","mondo","0015748"
> "3613","Canavan disease","mesh","D017825"
> "3613","Canavan disease","umls","C0206307"
> "3613","Canavan disease","mondo","0010079"
> "0080278","Joubert syndrome 32","mondo","0033309"
> "0080279","Joubert syndrome 33","mondo","0033311"
> "0080274","multiple mitochondrial dysfunctions syndrome 5","mondo","0033282"
> "0080032","craniodiaphyseal dysplasia","mesh","C562940"
> "0080032","craniodiaphyseal dysplasia","mondo","0009031"
> "0080277","Joubert syndrome 31","mondo","0033310"
> "0080270","autosomal dominant nonsyndromic deafness 34","mondo","0033261"
> "0080271","nephrotic syndrome type 15","mondo","0033262"
> "0080272","nephrotic syndrome type 16","mondo","0033280"
> "0080033","craniometaphyseal dysplasia","mondo","0015465"
> "4707","cervicomedullary junction neoplasm","umls","C1332923"
> "4707","cervicomedullary junction neoplasm","mondo","0003108"
11137,11170c25049,25065
< "2326","gastroenteritis","icd10cm","K52.9"
< "2326","gastroenteritis","mesh","D005759"
< "2326","gastroenteritis","umls","C0017160"
< "2326","gastroenteritis","mondo","0002269"
< "0110928","nemaline myopathy 2","mondo","0009725"
< "0110929","nemaline myopathy 9","mondo","0014326"
< "0110926","nemaline myopathy 1","mondo","0012239"
< "0110927","nemaline myopathy 3","mondo","0008070"
< "0110924","familial hemophagocytic lymphohistiocytosis 4","mondo","0011336"
< "0110925","familial hemophagocytic lymphohistiocytosis 5","mondo","0013135"
< "0110922","familial hemophagocytic lymphohistiocytosis 2","mondo","0011337"
< "0110923","familial hemophagocytic lymphohistiocytosis 3","mondo","0012146"
< "0110920","hereditary spherocytosis type 5","mondo","0012985"
< "0110921","familial hemophagocytic lymphohistiocytosis 1","mondo","0009974"
< "0110895","inflammatory bowel disease 14","mondo","0012832"
< "9562","primary ciliary dyskinesia","mesh","D002925"
< "9562","primary ciliary dyskinesia","umls","C0008780"
< "9562","primary ciliary dyskinesia","mondo","0016575"
< "7762","childhood multilocular cystic kidney neoplasm","umls","C1332983"
< "7762","childhood multilocular cystic kidney neoplasm","mondo","0004356"
< "1115","sarcoma","icd10cm","C49"
< "1115","sarcoma","icd9cm","171"
< "1115","sarcoma","icd9cm","171.9"
< "1115","sarcoma","umls","C0153519"
< "1115","sarcoma","mondo","0005089"
< "1895","allergic contact dermatitis of eyelid","icd9cm","373.32"
< "1895","allergic contact dermatitis of eyelid","umls","C0155178"
< "1895","allergic contact dermatitis of eyelid","mondo","0002138"
< "10955","strongyloidiasis","icd10cm","B78"
< "10955","strongyloidiasis","icd10cm","B78.9"
< "10955","strongyloidiasis","icd9cm","127.2"
< "10955","strongyloidiasis","mesh","D013322"
< "10955","strongyloidiasis","umls","C0038463"
< "10955","strongyloidiasis","mondo","0005974"
---
> "2320","obstructive lung disease","mesh","D008173"
> "2320","obstructive lung disease","umls","C0600260"
> "2320","obstructive lung disease","mondo","0002267"
> "2327","viral gastritis","umls","C0563238"
> "2327","viral gastritis","mondo","0002270"
> "4702","mongolian spot","mesh","D049328"
> "4702","mongolian spot","umls","C0265985"
> "4702","mongolian spot","mondo","0006582"
> "1569","mechanical ectropion","icd9cm","374.12"
> "1569","mechanical ectropion","umls","C0155194"
> "1569","mechanical ectropion","mondo","0002042"
> "0080031","fibrous dysplasia","mondo","0000845"
> "4708","foramen magnum meningioma","umls","C1333630"
> "4708","foramen magnum meningioma","mondo","0003109"
> "0050336","hypophosphatemia","mesh","D017674"
> "0050336","hypophosphatemia","mondo","0000313"
> "0050578","occult macular dystrophy","mondo","0013316"
11171a25067,25076
> "3764","Denys-Drash syndrome","mesh","D030321"
> "3764","Denys-Drash syndrome","umls","C0950121"
> "3764","Denys-Drash syndrome","mondo","0008682"
> "3765","pseudohermaphroditism","icd10cm","Q56"
> "3765","pseudohermaphroditism","icd10cm","Q56.3"
> "3765","pseudohermaphroditism","icd9cm","752.7"
> "3765","pseudohermaphroditism","mesh","D012734"
> "3765","pseudohermaphroditism","umls","C0021193"
> "3765","pseudohermaphroditism","umls","C0033804"
> "3765","pseudohermaphroditism","mondo","0005518"
11175a25081,25083
> "3767","vaginal discharge","mesh","D019522"
> "3767","vaginal discharge","umls","C0227791"
> "3767","vaginal discharge","mondo","0002770"
11178,11181c25086,25088
< "1116","pertussis","kegg","05133"
< "1116","pertussis","mesh","D001885"
< "1116","pertussis","umls","C0006015"
< "1116","pertussis","mondo","0005077"
---
> "0050573","2-hydroxyglutaric aciduria","mondo","0016001"
> "0050570","congenital disorder of glycosylation type I","mondo","0005500"
> "0050571","congenital disorder of glycosylation type II","mondo","0005501"
11186,11206c25093,25096
< "0110823","hereditary spastic paraplegia 8","icd10cm","G11.4"
< "0110823","hereditary spastic paraplegia 8","mondo","0011339"
< "0110822","hereditary spastic paraplegia 77","icd10cm","G11.4"
< "0110822","hereditary spastic paraplegia 77","mondo","0014882"
< "0110821","hereditary spastic paraplegia 76","mondo","0014827"
< "8872","penis carcinoma in situ","icd10cm","D00-D09"
< "8872","penis carcinoma in situ","icd10cm","D07.4"
< "8872","penis carcinoma in situ","icd9cm","233.5"
< "8872","penis carcinoma in situ","umls","C0154089"
< "8872","penis carcinoma in situ","mondo","0004671"
< "0110827","Usher syndrome type 2","mesh","D052245"
< "0110827","Usher syndrome type 2","umls","C0339534"
< "0110827","Usher syndrome type 2","umls","C1568249"
< "0110827","Usher syndrome type 2","mondo","0016484"
< "0050779","hydrolethalus syndrome","icd10cm","Q87.8"
< "0050779","hydrolethalus syndrome","mesh","C536079"
< "0050779","hydrolethalus syndrome","mondo","0006037"
< "0110825","hereditary spastic paraplegia 9B","icd10cm","G11.4"
< "0110825","hereditary spastic paraplegia 9B","mondo","0014702"
< "0110824","hereditary spastic paraplegia 9A","icd10cm","G11.4"
< "0110824","hereditary spastic paraplegia 9A","mondo","0011006"
---
> "0050575","D-2-hydroxyglutaric aciduria","mondo","0010924"
> "0050332","enlarged vestibular aqueduct","mondo","0023069"
> "1293","labia minora carcinoma","umls","C1334357"
> "1293","labia minora carcinoma","mondo","0001602"
11208,11218c25098,25105
< "0050776","non-syndromic X-linked intellectual disability","mondo","0019181"
< "0050777","Joubert syndrome","icd10cm","Q04.3"
< "0050777","Joubert syndrome","mondo","0018772"
< "0050770","polycystic liver disease","mondo","0000447"
< "0050771","pheochromocytoma","mondo","0008233"
< "0050773","paraganglioma","mesh","D010235"
< "0050773","paraganglioma","umls","C0030421"
< "0050773","paraganglioma","mondo","0000448"
< "0110804","hereditary spastic paraplegia 52","mondo","0013552"
< "6017","central nervous system mature teratoma","umls","C1332886"
< "6017","central nervous system mature teratoma","mondo","0003733"
---
> "2498","tooth erosion","icd10cm","K03.2"
> "2498","tooth erosion","icd9cm","521.3"
> "2498","tooth erosion","mesh","D014077"
> "2498","tooth erosion","umls","C0040436"
> "2498","tooth erosion","mondo","0002325"
> "4648","familial retinoblastoma","mesh","D012175"
> "4648","familial retinoblastoma","umls","C0751483"
> "4648","familial retinoblastoma","mondo","0018160"
11223a25111,25120
> "2490","congenital nervous system abnormality","icd9cm","742"
> "2490","congenital nervous system abnormality","umls","C0158538"
> "2490","congenital nervous system abnormality","mondo","0002320"
> "4640","axillary adenitis","umls","C0919797"
> "4640","axillary adenitis","mondo","0003070"
> "13550","angle-closure glaucoma","mesh","D015812"
> "13550","angle-closure glaucoma","umls","C0017605"
> "13550","angle-closure glaucoma","mondo","0001744"
> "2495","senile angioma","umls","C0343082"
> "2495","senile angioma","mondo","0002323"
11231,11312c25128,25174
< "13521","tetanus neonatorum","icd10cm","A33"
< "13521","tetanus neonatorum","icd9cm","771.3"
< "13521","tetanus neonatorum","umls","C0343312"
< "13521","tetanus neonatorum","mondo","0001737"
< "0111068","congenital bile acid synthesis defect 4","mesh","C535444"
< "0111068","congenital bile acid synthesis defect 4","umls","C1858328"
< "0111068","congenital bile acid synthesis defect 4","mondo","0008967"
< "0111069","congenital bile acid synthesis defect 2","mesh","C535443"
< "0111069","congenital bile acid synthesis defect 2","umls","C1856127"
< "0111069","congenital bile acid synthesis defect 2","mondo","0009339"
< "0111064","autosomal recessive distal spinal muscular atrophy 1","icd10cm","G12.2"
< "0111064","autosomal recessive distal spinal muscular atrophy 1","mondo","0011436"
< "0111065","autosomal recessive distal spinal muscular atrophy 2","mesh","C535715"
< "0111065","autosomal recessive distal spinal muscular atrophy 2","umls","C1854023"
< "0111065","autosomal recessive distal spinal muscular atrophy 2","mondo","0011585"
< "0111066","congenital bile acid synthesis defect 5","mondo","0014564"
< "0111067","congenital bile acid synthesis defect 6","mondo","0015015"
< "0111060","Ambras type hypertrichosis universalis congenita","icd10cm","Q84.2"
< "0111060","Ambras type hypertrichosis universalis congenita","mesh","C536605"
< "0111060","Ambras type hypertrichosis universalis congenita","mondo","0007787"
< "3241","lipid pneumonia","icd10cm","J69.1"
< "3241","lipid pneumonia","mesh","D011017"
< "3241","lipid pneumonia","umls","C0032298"
< "3241","lipid pneumonia","mondo","0005826"
< "0111062","familial hypobetalipoproteinemia 1","mondo","0014252"
< "0111063","hyperphosphatemic familial tumoral calcinosis","icd10cm","M11.2"
< "0111063","hyperphosphatemic familial tumoral calcinosis","mondo","0008897"
< "9263","homocystinuria","icd10cm","E72.11"
< "9263","homocystinuria","mesh","D006712"
< "9263","homocystinuria","umls","C0019880"
< "9263","homocystinuria","mondo","0004737"
< "2476","hereditary spastic paraplegia","icd10cm","G11.4"
< "2476","hereditary spastic paraplegia","icd9cm","334.1"
< "2476","hereditary spastic paraplegia","mesh","D015419"
< "2476","hereditary spastic paraplegia","umls","C0037773"
< "2476","hereditary spastic paraplegia","mondo","0019064"
< "9261","nasopharynx carcinoma","icd10cm","C11"
< "9261","nasopharynx carcinoma","icd10cm","C11.0"
< "9261","nasopharynx carcinoma","icd10cm","C11.1"
< "9261","nasopharynx carcinoma","icd10cm","C11.2"
< "9261","nasopharynx carcinoma","icd10cm","C11.3"
< "9261","nasopharynx carcinoma","icd10cm","C11.9"
< "9261","nasopharynx carcinoma","icd9cm","147"
< "9261","nasopharynx carcinoma","icd9cm","147.0"
< "9261","nasopharynx carcinoma","icd9cm","147.1"
< "9261","nasopharynx carcinoma","icd9cm","147.2"
< "9261","nasopharynx carcinoma","icd9cm","147.3"
< "9261","nasopharynx carcinoma","icd9cm","147.9"
< "9261","nasopharynx carcinoma","mesh","D009303"
< "9261","nasopharynx carcinoma","umls","C0153392"
< "9261","nasopharynx carcinoma","umls","C0153393"
< "9261","nasopharynx carcinoma","umls","C0153394"
< "9261","nasopharynx carcinoma","umls","C0153395"
< "9261","nasopharynx carcinoma","umls","C0153396"
< "9261","nasopharynx carcinoma","umls","C0238301"
< "9261","nasopharynx carcinoma","mondo","0015459"
< "3240","aspiration pneumonitis","icd10cm","J69.0"
< "3240","aspiration pneumonitis","mesh","D011015"
< "3240","aspiration pneumonitis","umls","C0032290"
< "3240","aspiration pneumonitis","mondo","0002572"
< "2473","opportunistic mycosis","icd9cm","118"
< "2473","opportunistic mycosis","umls","C0029119"
< "2473","opportunistic mycosis","mondo","0002312"
< "9265","histidine metabolism disease","icd10cm","E70.4"
< "9265","histidine metabolism disease","icd10cm","E70.40"
< "9265","histidine metabolism disease","icd9cm","270.5"
< "9265","histidine metabolism disease","umls","C0268512"
< "9265","histidine metabolism disease","mondo","0019228"
< "9269","maple syrup urine disease","icd10cm","E71.0"
< "9269","maple syrup urine disease","mesh","D008375"
< "9269","maple syrup urine disease","umls","C0024776"
< "9269","maple syrup urine disease","mondo","0009563"
< "9268","glycine encephalopathy","icd10cm","E72.51"
< "9268","glycine encephalopathy","mesh","D020158"
< "9268","glycine encephalopathy","umls","C0751748"
< "9268","glycine encephalopathy","mondo","0011612"
< "986","alopecia areata","icd10cm","L63"
< "986","alopecia areata","icd10cm","L63.9"
< "986","alopecia areata","icd9cm","704.01"
< "986","alopecia areata","mesh","D000506"
< "986","alopecia areata","umls","C0002171"
< "986","alopecia areata","mondo","0005340"
---
> "4645","retinal cancer","icd10cm","C69.2"
> "4645","retinal cancer","icd9cm","190.5"
> "4645","retinal cancer","mesh","D019572"
> "4645","retinal cancer","umls","C0024622"
> "4645","retinal cancer","umls","C0524801"
> "4645","retinal cancer","mondo","0003072"
> "0070233","Loeys-Dietz syndrome 4","mondo","0013897"
> "11771","spontaneous ocular nystagmus","icd10cm","H55.03"
> "11771","spontaneous ocular nystagmus","icd9cm","379.53"
> "11771","spontaneous ocular nystagmus","mesh","D009759"
> "11771","spontaneous ocular nystagmus","umls","C0271384"
> "11771","spontaneous ocular nystagmus","mondo","0001361"
> "7894","mite infestation","icd10cm","B88.0"
> "7894","mite infestation","icd10cm","B88.9"
> "7894","mite infestation","icd9cm","133"
> "7894","mite infestation","icd9cm","133.9"
> "7894","mite infestation","mesh","D008924"
> "7894","mite infestation","umls","C0026229"
> "7894","mite infestation","mondo","0004389"
> "11772","leukocoria","icd10cm","H44.53"
> "11772","leukocoria","icd9cm","360.44"
> "11772","leukocoria","umls","C0152458"
> "11772","leukocoria","mondo","0001362"
> "11776","blind hypertensive eye","icd9cm","360.42"
> "11776","blind hypertensive eye","umls","C0154789"
> "11776","blind hypertensive eye","mondo","0001363"
> "0070150","hereditary sensory and autonomic neuropathy type 2B","mondo","0013142"
> "5158","pleural cancer","icd10cm","C38.4"
> "5158","pleural cancer","icd9cm","163"
> "5158","pleural cancer","icd9cm","163.9"
> "5158","pleural cancer","mesh","D010997"
> "5158","pleural cancer","umls","C0032229"
> "5158","pleural cancer","umls","C0153494"
> "5158","pleural cancer","mondo","0006294"
> "14463","cavernous hemangioma of orbit","umls","C0346352"
> "14463","cavernous hemangioma of orbit","mondo","0001975"
> "5151","plexiform neurofibroma","mesh","D018318"
> "5151","plexiform neurofibroma","umls","C0206728"
> "5151","plexiform neurofibroma","mondo","0003304"
> "5150","neurofibroma of gallbladder","umls","C1333751"
> "5150","neurofibroma of gallbladder","mondo","0003303"
> "5153","atypical neurofibroma","umls","C1510961"
> "5153","atypical neurofibroma","mondo","0003306"
> "5152","cellular neurofibroma","umls","C1516371"
> "5152","cellular neurofibroma","mondo","0003305"
> "5155","multiple mucosal neuroma","umls","C1334828"
> "5155","multiple mucosal neuroma","mondo","0003307"
11316,11330c25178,25189
< "2479","central nervous system origin vertigo","icd10cm","H81.4"
< "2479","central nervous system origin vertigo","icd10cm","H81.49"
< "2479","central nervous system origin vertigo","icd9cm","386.2"
< "2479","central nervous system origin vertigo","mesh","D014717"
< "2479","central nervous system origin vertigo","umls","C0155503"
< "2479","central nervous system origin vertigo","mondo","0002317"
< "10047","nodular malignant melanoma","umls","C0334424"
< "10047","nodular malignant melanoma","mondo","0000930"
< "0050118","La Crosse encephalitis","icd10cm","A83.5"
< "0050118","La Crosse encephalitis","icd9cm","062.5"
< "0050118","La Crosse encephalitis","mesh","D004670"
< "0050118","La Crosse encephalitis","umls","C0014053"
< "0050118","La Crosse encephalitis","mondo","0019378"
< "0110812","hereditary spastic paraplegia 61","icd10cm","G11.4"
< "0110812","hereditary spastic paraplegia 61","mondo","0014304"
---
> "5157","benign pleural mesothelioma","umls","C1377913"
> "5157","benign pleural mesothelioma","mondo","0003308"
> "115","cardiac tamponade","icd10cm","I31.4"
> "115","cardiac tamponade","icd9cm","423.3"
> "115","cardiac tamponade","mesh","D002305"
> "115","cardiac tamponade","umls","C0007177"
> "115","cardiac tamponade","mondo","0001297"
> "114","heart disease","icd10cm","I51.9"
> "114","heart disease","icd9cm","429.9"
> "114","heart disease","mesh","D006331"
> "114","heart disease","umls","C0018799"
> "114","heart disease","mondo","0005267"
11337,11344c25196,25213
< "0080302","mixed sleep apnea","mesh","D012891"
< "0080302","mixed sleep apnea","umls","C0338495"
< "0080302","mixed sleep apnea","mondo","0024358"
< "0060800","syndromic X-linked intellectual disability 5","mesh","C535773"
< "0060800","syndromic X-linked intellectual disability 5","umls","C0796254"
< "0060800","syndromic X-linked intellectual disability 5","mondo","0010574"
< "0050741","alcohol dependence","kegg","05034"
< "0050741","alcohol dependence","mondo","0007079"
---
> "116","pericardium cancer","icd10cm","C38.0"
> "116","pericardium cancer","umls","C0346609"
> "116","pericardium cancer","umls","C0349574"
> "116","pericardium cancer","mondo","0001322"
> "110","lens disease","icd10cm","H25-H28"
> "110","lens disease","icd10cm","H27.9"
> "110","lens disease","mesh","D007905"
> "110","lens disease","umls","C0023308"
> "110","lens disease","mondo","0001176"
> "112","esophageal varix","icd10cm","I85.01"
> "112","esophageal varix","icd9cm","456.0"
> "112","esophageal varix","icd9cm","456.2"
> "112","esophageal varix","icd9cm","456.20"
> "112","esophageal varix","umls","C0155789"
> "112","esophageal varix","umls","C0155791"
> "112","esophageal varix","umls","C0155792"
> "112","esophageal varix","mondo","0001221"
> "0070234","Loeys-Dietz syndrome 2","mondo","0012427"
11351,11479c25220,25240
< "0110810","hereditary spastic paraplegia 5A","icd10cm","G11.4"
< "0110810","hereditary spastic paraplegia 5A","mondo","0010047"
< "0050117","disease by infectious agent","icd9cm","079.0"
< "0050117","disease by infectious agent","umls","C0001485"
< "0050117","disease by infectious agent","mondo","0005550"
< "0080094","myofibrillar myopathy 3","icd10cm","G71.0"
< "0080094","myofibrillar myopathy 3","mondo","0012215"
< "0080095","myofibrillar myopathy 4","mondo","0012277"
< "0080096","myofibrillar myopathy 5","mondo","0012289"
< "0110811","hereditary spastic paraplegia 6","icd10cm","G11.4"
< "0110811","hereditary spastic paraplegia 6","mondo","0010878"
< "0110629","Wolfram syndrome 1","icd10cm","E13.8"
< "0110629","Wolfram syndrome 1","mondo","0009101"
< "0110628","primary ciliary dyskinesia 24","icd10cm","Q34.8"
< "0110628","primary ciliary dyskinesia 24","mondo","0014202"
< "0080092","myofibrillar myopathy 1","icd10cm","G71.0"
< "0080092","myofibrillar myopathy 1","mondo","0011076"
< "12399","pathological gambling","icd10cm","F63.0"
< "12399","pathological gambling","icd9cm","312.31"
< "12399","pathological gambling","mesh","D005715"
< "12399","pathological gambling","umls","C0030662"
< "12399","pathological gambling","mondo","0011662"
< "0110625","primary ciliary dyskinesia 20","icd10cm","Q34.8"
< "0110625","primary ciliary dyskinesia 20","mondo","0014030"
< "0110816","hereditary spastic paraplegia 7","icd10cm","G11.4"
< "0110816","hereditary spastic paraplegia 7","mondo","0011803"
< "0110627","primary ciliary dyskinesia 26","icd10cm","Q34.8"
< "0110627","primary ciliary dyskinesia 26","mondo","0014211"
< "0110626","primary ciliary dyskinesia 2","icd10cm","Q34.8"
< "0110626","primary ciliary dyskinesia 2","mondo","0011718"
< "0110621","primary ciliary dyskinesia 17","icd10cm","Q34.8"
< "0110621","primary ciliary dyskinesia 17","mondo","0013854"
< "0110620","primary ciliary dyskinesia 35","mondo","0014910"
< "0110623","primary ciliary dyskinesia 15","icd10cm","Q34.8"
< "0110623","primary ciliary dyskinesia 15","mondo","0013435"
< "0110622","primary ciliary dyskinesia 9","icd10cm","Q34.8"
< "0110622","primary ciliary dyskinesia 9","mondo","0012906"
< "0050682","Athabaskan brainstem dysgenesis syndrome","mondo","0011099"
< "10600","chronic tic disorder","icd10cm","F95.1"
< "10600","chronic tic disorder","icd9cm","307.22"
< "10600","chronic tic disorder","mesh","D013981"
< "10600","chronic tic disorder","umls","C0008701"
< "10600","chronic tic disorder","mondo","0001074"
< "10606","blind loop syndrome","icd10cm","K90.2"
< "10606","blind loop syndrome","icd9cm","579.2"
< "10606","blind loop syndrome","mesh","D001765"
< "10606","blind loop syndrome","umls","C0005750"
< "10606","blind loop syndrome","mondo","0005673"
< "0060807","syndromic X-linked intellectual disability Najm type","icd10cm","Q04.3"
< "0060807","syndromic X-linked intellectual disability Najm type","mondo","0010417"
< "11603","infant gynecomastia","icd10cm","P83.4"
< "11603","infant gynecomastia","icd9cm","778.7"
< "11603","infant gynecomastia","mesh","D006177"
< "11603","infant gynecomastia","umls","C1449721"
< "11603","infant gynecomastia","mondo","0001323"
< "9462","cholesteatoma of external ear","icd10cm","H60.4"
< "9462","cholesteatoma of external ear","icd10cm","H60.40"
< "9462","cholesteatoma of external ear","icd9cm","380.21"
< "9462","cholesteatoma of external ear","umls","C0155398"
< "9462","cholesteatoma of external ear","mondo","0006532"
< "12155","lymphocytic choriomeningitis","icd10cm","A87.2"
< "12155","lymphocytic choriomeningitis","mesh","D008216"
< "12155","lymphocytic choriomeningitis","umls","C0024266"
< "12155","lymphocytic choriomeningitis","mondo","0001449"
< "10608","celiac disease","icd10cm","K90.0"
< "10608","celiac disease","icd9cm","579.0"
< "10608","celiac disease","mesh","D002446"
< "10608","celiac disease","umls","C0007570"
< "10608","celiac disease","mondo","0005130"
< "12157","aseptic meningitis","icd10cm","G03.0"
< "12157","aseptic meningitis","mesh","D008582"
< "12157","aseptic meningitis","umls","C0025290"
< "12157","aseptic meningitis","mondo","0006662"
< "2211","factor XIII deficiency","mesh","D005177"
< "2211","factor XIII deficiency","umls","C0015530"
< "2211","factor XIII deficiency","mondo","0018029"
< "9087","anal carcinoma in situ","icd9cm","230.6"
< "9087","anal carcinoma in situ","umls","C0154064"
< "9087","anal carcinoma in situ","mondo","0004707"
< "10595","Charcot-Marie-Tooth disease","icd10cm","G60.0"
< "10595","Charcot-Marie-Tooth disease","icd9cm","356.1"
< "10595","Charcot-Marie-Tooth disease","mesh","D002607"
< "10595","Charcot-Marie-Tooth disease","umls","C0007959"
< "10595","Charcot-Marie-Tooth disease","mondo","0015626"
< "0050683","Bothnia retinal dystrophy","mondo","0011838"
< "13254","diverticulitis of colon","mesh","D004239"
< "13254","diverticulitis of colon","umls","C0012814"
< "13254","diverticulitis of colon","mondo","0001674"
< "0050606","acrokeratosis verruciformis","mondo","0007048"
< "0050600","ABCD syndrome","mondo","0010895"
< "0050601","ADULT syndrome","mondo","0007072"
< "0050602","triple-A syndrome","mondo","0009279"
< "0050603","acheiropody","mondo","0008700"
< "10426","Klippel-Feil syndrome","icd10cm","Q76.1"
< "10426","Klippel-Feil syndrome","icd9cm","756.16"
< "10426","Klippel-Feil syndrome","mesh","D007714"
< "10426","Klippel-Feil syndrome","umls","C0022738"
< "10426","Klippel-Feil syndrome","mondo","0001029"
< "9312","chronic ethmoiditis","icd10cm","J32.2"
< "9312","chronic ethmoiditis","icd9cm","473.2"
< "9312","chronic ethmoiditis","umls","C0008681"
< "9312","chronic ethmoiditis","mondo","0004757"
< "9643","babesiosis","icd10cm","B60.0"
< "9643","babesiosis","icd9cm","088.82"
< "9643","babesiosis","mesh","D001404"
< "9643","babesiosis","umls","C0004576"
< "9643","babesiosis","mondo","0005661"
< "8956","cowpox","icd10cm","B08.010"
< "8956","cowpox","icd9cm","051.01"
< "8956","cowpox","mesh","D015605"
< "8956","cowpox","umls","C0010232"
< "8956","cowpox","mondo","0005720"
< "0110488","autosomal recessive nonsyndromic deafness 3","icd10cm","H90.3"
< "0110488","autosomal recessive nonsyndromic deafness 3","mondo","0010860"
< "0050597","intestinal schistosomiasis","icd10cm","B65.1"
< "0050597","intestinal schistosomiasis","icd10cm","B65.2"
< "0050597","intestinal schistosomiasis","icd9cm","120.1"
< "0050597","intestinal schistosomiasis","icd9cm","120.2"
< "0050597","intestinal schistosomiasis","mesh","D012554"
< "0050597","intestinal schistosomiasis","mesh","D012555"
< "0050597","intestinal schistosomiasis","umls","C0036329"
< "0050597","intestinal schistosomiasis","umls","C0036330"
< "0050597","intestinal schistosomiasis","umls","C0276932"
< "0050597","intestinal schistosomiasis","mondo","0008412"
< "0050591","tooth agenesis","icd10cm","K00.0"
< "0050591","tooth agenesis","icd9cm","520.0"
< "0050591","tooth agenesis","mesh","D000848"
< "0050591","tooth agenesis","umls","C0399352"
< "0050591","tooth agenesis","mondo","0005486"
---
> "118","pericardial effusion","mesh","D010490"
> "118","pericardial effusion","umls","C0031039"
> "118","pericardial effusion","mondo","0001370"
> "12305","Bloch-Sulzberger syndrome","icd10cm","Q82.3"
> "12305","Bloch-Sulzberger syndrome","mesh","D007184"
> "12305","Bloch-Sulzberger syndrome","umls","C0021171"
> "12305","Bloch-Sulzberger syndrome","mondo","0010631"
> "12304","conjunctival pigmentation","icd10cm","H11.13"
> "12304","conjunctival pigmentation","icd9cm","372.55"
> "12304","conjunctival pigmentation","umls","C0155163"
> "12304","conjunctival pigmentation","mondo","0006537"
> "1932","Angelman syndrome","icd10cm","Q93.5"
> "1932","Angelman syndrome","mesh","D017204"
> "1932","Angelman syndrome","umls","C0162635"
> "1932","Angelman syndrome","mondo","0007113"
> "0111587","Gordon Holmes syndrome","mesh","C565870"
> "0111587","Gordon Holmes syndrome","umls","C1859305"
> "12550","hepatic coma","icd10cm","K72.91"
> "12550","hepatic coma","mesh","D006501"
> "12550","hepatic coma","umls","C0019147"
> "12550","hepatic coma","mondo","0001548"
11484,11489c25245,25247
< "0110481","autosomal recessive nonsyndromic deafness 23","icd10cm","H90.3"
< "0110481","autosomal recessive nonsyndromic deafness 23","mondo","0012293"
< "0110480","autosomal recessive nonsyndromic deafness 22","icd10cm","H90.3"
< "0110480","autosomal recessive nonsyndromic deafness 22","mondo","0011762"
< "3502","ampulla of Vater adenocarcinoma","umls","C1332243"
< "3502","ampulla of Vater adenocarcinoma","mondo","0002670"
---
> "0070196","infantile-onset distal myopathy","mondo","0008049"
> "0070197","distal myopathy 1","mondo","0008050"
> "0070194","autosomal recessive chronic granulomatous disease cytochrome b-positive type III","mondo","0013507"
11491,11492c25249
< "0110485","autosomal recessive nonsyndromic deafness 27","icd10cm","H90.3"
< "0110485","autosomal recessive nonsyndromic deafness 27","mondo","0011602"
---
> "0070192","autosomal recessive chronic granulomatous disease cytochrome b-positive type I","mondo","0009309"
11494,11497c25251,25252
< "0110487","autosomal recessive nonsyndromic deafness 29","icd10cm","H90.3"
< "0110487","autosomal recessive nonsyndromic deafness 29","mondo","0013537"
< "0110486","autosomal recessive nonsyndromic deafness 28","icd10cm","H90.3"
< "0110486","autosomal recessive nonsyndromic deafness 28","mondo","0012355"
---
> "0070190","autosomal dominant chronic granulomatous disease","mondo","0007684"
> "0070191","autosomal recessive chronic granulomatous disease cytochrome b-positive type II","mondo","0009310"
11502,11507c25257,25261
< "0070271","Lynch syndrome 1","mondo","0007356"
< "9790","toxocariasis","icd10cm","B83.0"
< "9790","toxocariasis","mesh","D007816"
< "9790","toxocariasis","mesh","D014120"
< "9790","toxocariasis","umls","C0023049"
< "9790","toxocariasis","mondo","0005988"
---
> "0111581","C syndrome","mesh","C537418"
> "0111581","C syndrome","umls","C0796095"
> "2560","morphine dependence","mesh","D009021"
> "2560","morphine dependence","umls","C0026552"
> "2560","morphine dependence","mondo","0005531"
11522,11548c25276,25290
< "8557","oropharynx cancer","icd10cm","C10"
< "8557","oropharynx cancer","icd10cm","C10.2"
< "8557","oropharynx cancer","icd10cm","C10.3"
< "8557","oropharynx cancer","icd10cm","C10.8"
< "8557","oropharynx cancer","icd10cm","C10.9"
< "8557","oropharynx cancer","icd9cm","146"
< "8557","oropharynx cancer","icd9cm","146.5"
< "8557","oropharynx cancer","icd9cm","146.6"
< "8557","oropharynx cancer","icd9cm","146.7"
< "8557","oropharynx cancer","icd9cm","146.9"
< "8557","oropharynx cancer","umls","C0153382"
< "8557","oropharynx cancer","umls","C0153388"
< "8557","oropharynx cancer","umls","C0153389"
< "8557","oropharynx cancer","umls","C0153390"
< "8557","oropharynx cancer","mondo","0004608"
< "0110311","hypertrophic cardiomyopathy 21","mondo","0013852"
< "0110310","hypertrophic cardiomyopathy 4","mondo","0007268"
< "0110313","hypertrophic cardiomyopathy 7","mondo","0013369"
< "0111131","focal segmental glomerulosclerosis 6","icd10cm","N04.1"
< "0111131","focal segmental glomerulosclerosis 6","mondo","0013589"
< "0110315","hypertrophic cardiomyopathy 9","mondo","0013412"
< "0110314","hypertrophic cardiomyopathy 8","mondo","0012111"
< "0110317","hypertrophic cardiomyopathy 11","mondo","0012799"
< "0110316","hypertrophic cardiomyopathy 10","mondo","0012112"
< "0110319","hypertrophic cardiomyopathy 13","mondo","0013195"
< "0111136","congenital generalized lipodystrophy type 2","icd10cm","E88.1"
< "0111136","congenital generalized lipodystrophy type 2","mondo","0010020"
---
> "8009","penis mixed squamous cell carcinoma","umls","C1513369"
> "8009","penis mixed squamous cell carcinoma","mondo","0004430"
> "2562","suppurative periapical periodontitis","mesh","D010482"
> "2562","suppurative periapical periodontitis","umls","C0031024"
> "2562","suppurative periapical periodontitis","mondo","0006989"
> "6837","rete ovarii adenoma","umls","C1514905"
> "6837","rete ovarii adenoma","mondo","0004005"
> "12800","mucopolysaccharidosis VI","mesh","D009087"
> "12800","mucopolysaccharidosis VI","umls","C0026709"
> "12800","mucopolysaccharidosis VI","mondo","0009661"
> "2565","macular corneal dystrophy","icd10cm","H18.55"
> "2565","macular corneal dystrophy","icd9cm","371.55"
> "2565","macular corneal dystrophy","mesh","D003317"
> "2565","macular corneal dystrophy","umls","C0024439"
> "2565","macular corneal dystrophy","mondo","0009020"
11551,11556c25293,25294
< "10763","hypertension","icd10cm","I10"
< "10763","hypertension","icd9cm","401-405.99"
< "10763","hypertension","icd9cm","997.91"
< "10763","hypertension","mesh","D006973"
< "10763","hypertension","umls","C0020538"
< "10763","hypertension","mondo","0005044"
---
> "6838","rete ovarii cystadenofibroma","umls","C1514906"
> "6838","rete ovarii cystadenofibroma","mondo","0004006"
11570,11606c25308,25315
< "1252","trichuriasis","icd10cm","B79"
< "1252","trichuriasis","icd9cm","127.3"
< "1252","trichuriasis","mesh","D014257"
< "1252","trichuriasis","umls","C0040954"
< "1252","trichuriasis","mondo","0005996"
< "2907","Goldenhar syndrome","icd10cm","Q87.0"
< "2907","Goldenhar syndrome","mesh","D006053"
< "2907","Goldenhar syndrome","umls","C0265240"
< "2907","Goldenhar syndrome","mondo","0008112"
< "1631","benign breast phyllodes tumor","icd10cm","D48.6"
< "1631","benign breast phyllodes tumor","mesh","D003557"
< "1631","benign breast phyllodes tumor","umls","C0010701"
< "1631","benign breast phyllodes tumor","umls","C0334501"
< "1631","benign breast phyllodes tumor","umls","C1332533"
< "1631","benign breast phyllodes tumor","mondo","0015871"
< "1634","breast papillomatosis","umls","C1332636"
< "1634","breast papillomatosis","mondo","0002063"
< "3211","lysosomal storage disease","mesh","D016464"
< "3211","lysosomal storage disease","umls","C0085078"
< "3211","lysosomal storage disease","mondo","0002561"
< "1638","central nervous system tuberculosis","icd9cm","013.2"
< "1638","central nervous system tuberculosis","icd9cm","013.20"
< "1638","central nervous system tuberculosis","mesh","D016862"
< "1638","central nervous system tuberculosis","mesh","D020306"
< "1638","central nervous system tuberculosis","umls","C0085388"
< "1638","central nervous system tuberculosis","mondo","0005696"
< "1639","skeletal tuberculosis","icd10cm","A18.0"
< "1639","skeletal tuberculosis","icd9cm","015"
< "1639","skeletal tuberculosis","icd9cm","015.9"
< "1639","skeletal tuberculosis","mesh","D014394"
< "1639","skeletal tuberculosis","umls","C0041324"
< "1639","skeletal tuberculosis","mondo","0005962"
< "0110557","autosomal dominant nonsyndromic deafness 28","icd10cm","H90.3"
< "0110557","autosomal dominant nonsyndromic deafness 28","mondo","0012083"
< "0110004","3-methylglutaconic aciduria type 3","mondo","0009787"
< "0110007","achromatopsia 2","mondo","0009003"
< "0110006","3-methylglutaconic aciduria type 4","mondo","0009611"
---
> "2566","corneal dystrophy","icd10cm","H18.5"
> "2566","corneal dystrophy","icd10cm","H18.50"
> "2566","corneal dystrophy","icd9cm","371.5"
> "2566","corneal dystrophy","icd9cm","371.50"
> "2566","corneal dystrophy","mesh","D003317"
> "2566","corneal dystrophy","umls","C0010035"
> "2566","corneal dystrophy","umls","C0010036"
> "2566","corneal dystrophy","mondo","0018102"
11611,11626c25320,25324
< "0110000","3-methylglutaconic aciduria type 5","mondo","0012435"
< "0110003","3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia","mondo","0014561"
< "0110002","3-methylglutaconic aciduria type 1","mondo","0009610"
< "12030","panuveitis","icd10cm","H44.11"
< "12030","panuveitis","icd9cm","360.12"
< "12030","panuveitis","mesh","D015864"
< "12030","panuveitis","umls","C0030343"
< "12030","panuveitis","mondo","0017255"
< "0110009","achromatopsia 7","mondo","0014677"
< "0110008","achromatopsia 3","mondo","0009875"
< "0110559","autosomal dominant nonsyndromic deafness 2B","icd10cm","H90.3"
< "0110559","autosomal dominant nonsyndromic deafness 2B","mondo","0012976"
< "0110558","autosomal dominant nonsyndromic deafness 2A","icd10cm","H90.3"
< "0110558","autosomal dominant nonsyndromic deafness 2A","mondo","0010817"
< "9445","cervix squamous papilloma","umls","C1336900"
< "9445","cervix squamous papilloma","mondo","0004788"
---
> "12809","chronic lacrimal gland enlargement","icd10cm","H04.03"
> "12809","chronic lacrimal gland enlargement","icd9cm","375.03"
> "12809","chronic lacrimal gland enlargement","umls","C1300133"
> "12809","chronic lacrimal gland enlargement","mondo","0001588"
> "0111206","distal hereditary motor neuronopathy type 2","umls","C3711384"
11637,11697c25335,25346
< "0050902","medulloblastoma","mesh","D008527"
< "0050902","medulloblastoma","mesh","D018242"
< "0050902","medulloblastoma","umls","C0025149"
< "0050902","medulloblastoma","umls","C0206663"
< "0050902","medulloblastoma","umls","C1334410"
< "0050902","medulloblastoma","mondo","0007959"
< "14705","Pfeiffer syndrome","mesh","D000168"
< "14705","Pfeiffer syndrome","umls","C0220658"
< "14705","Pfeiffer syndrome","mondo","0007043"
< "14256","adult-onset Still's disease","icd10cm","M06.1"
< "14256","adult-onset Still's disease","mesh","D016706"
< "14256","adult-onset Still's disease","umls","C0085253"
< "14256","adult-onset Still's disease","mondo","0019355"
< "14250","Down syndrome","icd10cm","Q90"
< "14250","Down syndrome","icd10cm","Q90.9"
< "14250","Down syndrome","icd9cm","758.0"
< "14250","Down syndrome","mesh","D004314"
< "14250","Down syndrome","umls","C0013080"
< "14250","Down syndrome","mondo","0008608"
< "12978","Plasmodium vivax malaria","icd10cm","B51"
< "12978","Plasmodium vivax malaria","icd10cm","B51.9"
< "12978","Plasmodium vivax malaria","icd9cm","084.1"
< "12978","Plasmodium vivax malaria","mesh","D016780"
< "12978","Plasmodium vivax malaria","umls","C0024537"
< "12978","Plasmodium vivax malaria","mondo","0005921"
< "0050909","MALT lymphoma","mondo","0007650"
< "0110338","osteogenesis imperfecta type 17","icd10cm","Q78.0"
< "0110338","osteogenesis imperfecta type 17","mondo","0014672"
< "12971","hereditary spherocytosis","icd10cm","D58.0"
< "12971","hereditary spherocytosis","icd9cm","282.0"
< "12971","hereditary spherocytosis","mesh","D013103"
< "12971","hereditary spherocytosis","umls","C0037889"
< "12971","hereditary spherocytosis","mondo","0019350"
< "0110479","autosomal recessive nonsyndromic deafness 21","icd10cm","H90.3"
< "0110479","autosomal recessive nonsyndromic deafness 21","mondo","0011351"
< "5425","ovarian hyperstimulation syndrome","mesh","D016471"
< "5425","ovarian hyperstimulation syndrome","umls","C0085083"
< "5425","ovarian hyperstimulation syndrome","mondo","0011972"
< "0070194","autosomal recessive chronic granulomatous disease cytochrome b-positive type III","mondo","0013507"
< "5426","premature ovarian failure","icd10cm","E28.3"
< "5426","premature ovarian failure","mesh","D016649"
< "5426","premature ovarian failure","umls","C0085215"
< "5426","premature ovarian failure","mondo","0005387"
< "5421","lung combined type small cell carcinoma","umls","C1333125"
< "5421","lung combined type small cell carcinoma","mondo","0003438"
< "3371","chondrosarcoma","mesh","D002813"
< "3371","chondrosarcoma","umls","C0008479"
< "3371","chondrosarcoma","umls","C1335473"
< "3371","chondrosarcoma","mondo","0008977"
< "6162","childhood embryonal testis carcinoma","umls","C1333007"
< "6162","childhood embryonal testis carcinoma","mondo","0003788"
< "0060359","Sakati-Nyhan syndrome","icd10cm","Q87.0"
< "0060359","Sakati-Nyhan syndrome","mesh","C537227"
< "0060359","Sakati-Nyhan syndrome","mondo","0007040"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","icd10cm","E71.313"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","mesh","D054069"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C0268596"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C1856401"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C1856403"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","umls","C1856405"
< "0060358","multiple acyl-CoA dehydrogenase deficiency","mondo","0009282"
---
> "7643","acantholytic squamous cell skin carcinoma","umls","C0345979"
> "7643","acantholytic squamous cell skin carcinoma","mondo","0004316"
> "7642","cholangiolocellular carcinoma","umls","C1516490"
> "7642","cholangiolocellular carcinoma","mondo","0004315"
> "7646","multiple spinal canal and spinal cord meningioma","umls","C1334825"
> "7646","multiple spinal canal and spinal cord meningioma","mondo","0004317"
> "5634","adenosquamous prostate carcinoma","umls","C1335503"
> "5634","adenosquamous prostate carcinoma","mondo","0003558"
> "10230","aortic atherosclerosis","icd10cm","I70.0"
> "10230","aortic atherosclerosis","icd9cm","440.0"
> "10230","aortic atherosclerosis","umls","C0155733"
> "10230","aortic atherosclerosis","mondo","0000980"
11705,11738c25354,25364
< "0060351","mitochondrial complex III deficiency nuclear type 2","mondo","0014063"
< "0060350","adenine phosphoribosyltransferase deficiency","mesh","C538228"
< "0060350","adenine phosphoribosyltransferase deficiency","umls","C0268120"
< "0060350","adenine phosphoribosyltransferase deficiency","umls","C3665382"
< "0060350","adenine phosphoribosyltransferase deficiency","mondo","0013869"
< "0060352","Kleefstra syndrome","mesh","C563043"
< "0060352","Kleefstra syndrome","umls","C0795833"
< "0060352","Kleefstra syndrome","mondo","0012455"
< "0060355","amyotrophic lateral sclerosis type 22","mondo","0014531"
< "0060354","Stormorken syndrome","mesh","C566108"
< "0060354","Stormorken syndrome","umls","C1861451"
< "0060354","Stormorken syndrome","mondo","0008497"
< "0060357","chylomicron retention disease","icd10cm","E78.3"
< "0060357","chylomicron retention disease","mesh","C535460"
< "0060357","chylomicron retention disease","umls","C0795956"
< "0060357","chylomicron retention disease","mondo","0009528"
< "0060356","Vici syndrome","mesh","C535566"
< "0060356","Vici syndrome","umls","C1855772"
< "0060356","Vici syndrome","mondo","0009452"
< "0070170","spermatogenic failure 19","mondo","0054723"
< "1166","palindromic rheumatism","icd10cm","M12.3"
< "1166","palindromic rheumatism","icd10cm","M12.30"
< "1166","palindromic rheumatism","icd9cm","719.3"
< "1166","palindromic rheumatism","icd9cm","719.30"
< "1166","palindromic rheumatism","icd9cm","719.31"
< "1166","palindromic rheumatism","mesh","C538103"
< "1166","palindromic rheumatism","umls","C0085574"
< "1166","palindromic rheumatism","umls","C0158178"
< "1166","palindromic rheumatism","mondo","0001332"
< "6496","extraskeletal myxoid chondrosarcoma","mesh","C563195"
< "6496","extraskeletal myxoid chondrosarcoma","umls","C1275278"
< "6496","extraskeletal myxoid chondrosarcoma","mondo","0012825"
< "6491","breast capillary hemangioma","umls","C1332619"
< "6491","breast capillary hemangioma","mondo","0003896"
---
> "1742","drug psychosis","icd9cm","292.1"
> "1742","drug psychosis","mesh","D011605"
> "1742","drug psychosis","umls","C0033937"
> "1742","drug psychosis","mondo","0006730"
> "10236","exhibitionism","icd10cm","F65.2"
> "10236","exhibitionism","icd9cm","302.4"
> "10236","exhibitionism","mesh","D005084"
> "10236","exhibitionism","umls","C0015269"
> "10236","exhibitionism","mondo","0000983"
> "7926","epithelial malignant thymoma","umls","C0279705"
> "7926","epithelial malignant thymoma","mondo","0006458"
11745,11800c25371,25413
< "6492","breast epithelioid hemangioma","umls","C1332627"
< "6492","breast epithelioid hemangioma","mondo","0003897"
< "13955","uterus interstitial leiomyoma","icd10cm","D25.1"
< "13955","uterus interstitial leiomyoma","icd9cm","218.1"
< "13955","uterus interstitial leiomyoma","umls","C0153994"
< "13955","uterus interstitial leiomyoma","mondo","0001843"
< "4242","kidney sarcoma","umls","C0346251"
< "4242","kidney sarcoma","mondo","0002930"
< "0070172","spermatogenic failure 15","mondo","0014847"
< "7389","pulmonary artery leiomyosarcoma","umls","C1335572"
< "7389","pulmonary artery leiomyosarcoma","mondo","0004207"
< "5520","head and neck squamous cell carcinoma","mesh","C535575"
< "5520","head and neck squamous cell carcinoma","umls","C1168401"
< "5520","head and neck squamous cell carcinoma","mondo","0010150"
< "5521","keratinizing squamous cell carcinoma","umls","C0334247"
< "5521","keratinizing squamous cell carcinoma","mondo","0005056"
< "5522","basaloid squamous cell carcinoma","umls","C1266005"
< "5522","basaloid squamous cell carcinoma","mondo","0003486"
< "6948","malignant gastric teratoma","umls","C1334151"
< "6948","malignant gastric teratoma","mondo","0004048"
< "0110103","atopic dermatitis 7","mondo","0013107"
< "5525","anal squamous cell carcinoma","umls","C1412036"
< "5525","anal squamous cell carcinoma","mondo","0006082"
< "5526","middle ear squamous cell carcinoma","umls","C1334762"
< "5526","middle ear squamous cell carcinoma","mondo","0006303"
< "5528","rectum squamous cell carcinoma","umls","C1335690"
< "5528","rectum squamous cell carcinoma","mondo","0018515"
< "2583","agammaglobulinemia","icd10cm","D80.1"
< "2583","agammaglobulinemia","icd9cm","279.00"
< "2583","agammaglobulinemia","mesh","D000361"
< "2583","agammaglobulinemia","umls","C0001768"
< "2583","agammaglobulinemia","umls","C0086438"
< "2583","agammaglobulinemia","mondo","0015977"
< "0050817","Stargardt disease","mondo","0019353"
< "0050530","intermediate spinal muscular atrophy","mondo","0009673"
< "14415","Legg-Calve-Perthes disease","icd10cm","M91.2"
< "14415","Legg-Calve-Perthes disease","icd10cm","M91.3"
< "14415","Legg-Calve-Perthes disease","mesh","D007873"
< "14415","Legg-Calve-Perthes disease","umls","C0022441"
< "14415","Legg-Calve-Perthes disease","umls","C0023234"
< "14415","Legg-Calve-Perthes disease","mondo","0007885"
< "14418","dracunculiasis","icd10cm","B72"
< "14418","dracunculiasis","icd9cm","125.7"
< "14418","dracunculiasis","mesh","D004320"
< "14418","dracunculiasis","umls","C0013100"
< "14418","dracunculiasis","mondo","0016472"
< "84","osteochondritis dissecans","icd10cm","M93.2"
< "84","osteochondritis dissecans","icd10cm","M93.9"
< "84","osteochondritis dissecans","icd9cm","732.7"
< "84","osteochondritis dissecans","mesh","D010007"
< "84","osteochondritis dissecans","mesh","D010008"
< "84","osteochondritis dissecans","umls","C0029420"
< "84","osteochondritis dissecans","umls","C0029421"
< "84","osteochondritis dissecans","mondo","0017178"
< "1293","labia minora carcinoma","umls","C1334357"
< "1293","labia minora carcinoma","mondo","0001602"
---
> "9132","liver carcinoma in situ","icd10cm","D01.5"
> "9132","liver carcinoma in situ","icd9cm","230.8"
> "9132","liver carcinoma in situ","umls","C0496854"
> "9132","liver carcinoma in situ","mondo","0004715"
> "10234","histoplasmosis pericarditis","icd9cm","115.93"
> "10234","histoplasmosis pericarditis","umls","C0153279"
> "10234","histoplasmosis pericarditis","mondo","0000981"
> "5494","epithelioid cell synovial sarcoma","umls","C0334506"
> "5494","epithelioid cell synovial sarcoma","mondo","0003469"
> "7293","mucin-rich endometrial endometrioid adenocarcinoma","umls","C1513711"
> "7293","mucin-rich endometrial endometrioid adenocarcinoma","mondo","0004175"
> "3307","teratoma","mesh","D013724"
> "3307","teratoma","umls","C0039538"
> "3307","teratoma","mondo","0002601"
> "0070174","spermatogenic failure 17","mondo","0014970"
> "14413","labyrinthine bilateral reactive loss","icd9cm","386.56"
> "14413","labyrinthine bilateral reactive loss","umls","C0155520"
> "14413","labyrinthine bilateral reactive loss","mondo","0001959"
> "11177","total internal ophthalmoplegia","icd9cm","367.52"
> "11177","total internal ophthalmoplegia","umls","C0152197"
> "11177","total internal ophthalmoplegia","mondo","0001211"
> "10648","acute inferoposterior infarction","icd9cm","410.30"
> "10648","acute inferoposterior infarction","umls","C0155640"
> "10648","acute inferoposterior infarction","mondo","0001088"
> "11175","enophthalmos","icd10cm","H05.4"
> "11175","enophthalmos","icd10cm","H05.40"
> "11175","enophthalmos","icd9cm","376.5"
> "11175","enophthalmos","icd9cm","376.50"
> "11175","enophthalmos","mesh","D015841"
> "11175","enophthalmos","umls","C0014306"
> "11175","enophthalmos","mondo","0001210"
> "7297","childhood extraosseous osteosarcoma","umls","C1332968"
> "7297","childhood extraosseous osteosarcoma","mondo","0004176"
> "10310","viral meningitis","icd10cm","A87"
> "10310","viral meningitis","icd10cm","A87.9"
> "10310","viral meningitis","icd9cm","047.9"
> "10310","viral meningitis","mesh","D008587"
> "10310","viral meningitis","umls","C0025297"
> "10310","viral meningitis","mondo","0007015"
> "1561","cognitive disorder","icd10cm","F09"
> "1561","cognitive disorder","mesh","D019965"
> "1561","cognitive disorder","umls","C0029227"
> "1561","cognitive disorder","mondo","0002039"
11805a25419,25423
> "1563","dermatomycosis","icd9cm","111"
> "1563","dermatomycosis","icd9cm","111.9"
> "1563","dermatomycosis","mesh","D003881"
> "1563","dermatomycosis","umls","C0011630"
> "1563","dermatomycosis","mondo","0002040"
11814,11884c25432,25458
< "7747","pediatric extraocular retinoblastoma","umls","C1321870"
< "7747","pediatric extraocular retinoblastoma","mondo","0004350"
< "0060649","congenital hereditary endothelial dystrophy of cornea","mondo","0009019"
< "9138","stomach carcinoma in situ","icd10cm","D00.2"
< "9138","stomach carcinoma in situ","icd9cm","230.2"
< "9138","stomach carcinoma in situ","umls","C0154060"
< "9138","stomach carcinoma in situ","mondo","0004716"
< "8398","osteoarthritis","icd9cm","715.3"
< "8398","osteoarthritis","mesh","D010003"
< "8398","osteoarthritis","umls","C0157946"
< "8398","osteoarthritis","mondo","0005178"
< "8849","sublingual gland cancer","icd10cm","C08.1"
< "8849","sublingual gland cancer","icd9cm","142.2"
< "8849","sublingual gland cancer","umls","C0153361"
< "8849","sublingual gland cancer","mondo","0004667"
< "0060642","recessive dystrophic epidermolysis bullosa","icd10cm","Q81.2"
< "0060642","recessive dystrophic epidermolysis bullosa","mondo","0009179"
< "0060641","endocrine-cerebro-osteodysplasia syndrome","icd10cm","Q87.8"
< "0060641","endocrine-cerebro-osteodysplasia syndrome","mondo","0012980"
< "0060647","cocoon syndrome","mondo","0013334"
< "0060645","chronic recurrent multifocal osteomyelitis","icd10cm","M86.3"
< "0060645","chronic recurrent multifocal osteomyelitis","mesh","C535456"
< "0060645","chronic recurrent multifocal osteomyelitis","mondo","0009813"
< "0060644","chondrodysplasia-pseudohermaphroditism syndrome","mesh","C536123"
< "0060644","chondrodysplasia-pseudohermaphroditism syndrome","umls","C1838654"
< "0060644","chondrodysplasia-pseudohermaphroditism syndrome","mondo","0010814"
< "8552","chronic myeloid leukemia","kegg","05220"
< "8552","chronic myeloid leukemia","icd9cm","205.1"
< "8552","chronic myeloid leukemia","mesh","D015464"
< "8552","chronic myeloid leukemia","umls","C0023473"
< "8552","chronic myeloid leukemia","mondo","0011996"
< "12804","mucopolysaccharidosis IV","icd10cm","E76.210"
< "12804","mucopolysaccharidosis IV","icd10cm","E76.219"
< "12804","mucopolysaccharidosis IV","mesh","D009085"
< "12804","mucopolysaccharidosis IV","umls","C0026707"
< "12804","mucopolysaccharidosis IV","umls","C0086651"
< "12804","mucopolysaccharidosis IV","mondo","0018938"
< "12554","hemolytic-uremic syndrome","icd10cm","D59.3"
< "12554","hemolytic-uremic syndrome","icd9cm","283.11"
< "12554","hemolytic-uremic syndrome","mesh","D006463"
< "12554","hemolytic-uremic syndrome","umls","C0019061"
< "12554","hemolytic-uremic syndrome","mondo","0001549"
< "12803","Sly syndrome","icd10cm","E76.29"
< "12803","Sly syndrome","mesh","D016538"
< "12803","Sly syndrome","umls","C0085132"
< "12803","Sly syndrome","mondo","0009662"
< "12556","acute kidney tubular necrosis","icd10cm","N17.0"
< "12556","acute kidney tubular necrosis","mesh","D007683"
< "12556","acute kidney tubular necrosis","umls","C0022672"
< "12556","acute kidney tubular necrosis","mondo","0006637"
< "12801","mucopolysaccharidosis III","icd10cm","E76.22"
< "12801","mucopolysaccharidosis III","mesh","D009084"
< "12801","mucopolysaccharidosis III","umls","C0026706"
< "12801","mucopolysaccharidosis III","umls","C0086647"
< "12801","mucopolysaccharidosis III","umls","C0086648"
< "12801","mucopolysaccharidosis III","mondo","0018937"
< "12559","idiopathic juvenile osteoporosis","icd9cm","733.02"
< "12559","idiopathic juvenile osteoporosis","umls","C0158447"
< "12559","idiopathic juvenile osteoporosis","mondo","0019409"
< "12800","mucopolysaccharidosis VI","mesh","D009087"
< "12800","mucopolysaccharidosis VI","umls","C0026709"
< "12800","mucopolysaccharidosis VI","mondo","0009661"
< "6278","ovarian mucinous malignant adenofibroma","mondo","0003839"
< "6543","acne","icd10cm","L70"
< "6543","acne","icd10cm","L70.2"
< "6543","acne","icd10cm","L70.9"
< "6543","acne","icd9cm","706.0"
< "6543","acne","mesh","D000152"
< "6543","acne","umls","C0152249"
< "6543","acne","umls","C0702166"
< "6543","acne","mondo","0011438"
---
> "7463","childhood pleomorphic rhabdomyosarcoma","umls","C0279614"
> "7463","childhood pleomorphic rhabdomyosarcoma","mondo","0004233"
> "10316","pneumoconiosis","icd10cm","J64"
> "10316","pneumoconiosis","icd9cm","505"
> "10316","pneumoconiosis","mesh","D011009"
> "10316","pneumoconiosis","umls","C0032273"
> "10316","pneumoconiosis","mondo","0015926"
> "13823","parasitic eyelid infestation","icd9cm","373.6"
> "13823","parasitic eyelid infestation","umls","C0155183"
> "13823","parasitic eyelid infestation","mondo","0001812"
> "13822","tetanic cataract","icd9cm","366.42"
> "13822","tetanic cataract","umls","C0039613"
> "13822","tetanic cataract","mondo","0001811"
> "13825","squamous blepharitis","icd10cm","H01.02"
> "13825","squamous blepharitis","icd9cm","373.02"
> "13825","squamous blepharitis","umls","C0155174"
> "13825","squamous blepharitis","mondo","0001813"
> "13351","pedophilia","icd10cm","F65.4"
> "13351","pedophilia","icd9cm","302.2"
> "13351","pedophilia","mesh","D010378"
> "13351","pedophilia","umls","C0030764"
> "13351","pedophilia","mondo","0001692"
> "5638","malignant giant cell tumor of soft parts","umls","C0334554"
> "5638","malignant giant cell tumor of soft parts","mondo","0003561"
> "5639","rete testis neoplasm","umls","C1514912"
> "5639","rete testis neoplasm","mondo","0003562"
> "0111397","congenital dyserythropoietic anemia type Ib","umls","C0271933"
11889a25464,25465
> "5635","gastric adenosquamous carcinoma","umls","C1333761"
> "5635","gastric adenosquamous carcinoma","mondo","0006034"
11896,11916c25472,25502
< "10969","hemiplegia","icd9cm","343.4"
< "10969","hemiplegia","mesh","D006429"
< "10969","hemiplegia","umls","C0392550"
< "10969","hemiplegia","mondo","0001170"
< "3197","schwannoma of twelfth cranial nerve","umls","C1335928"
< "3197","schwannoma of twelfth cranial nerve","mondo","0002549"
< "3196","cellular schwannoma","umls","C0431124"
< "3196","cellular schwannoma","mondo","0002548"
< "1362","paranasal sinus sarcoma","umls","C1335342"
< "1362","paranasal sinus sarcoma","mondo","0001758"
< "3191","nemaline myopathy","icd10cm","G71.2"
< "3191","nemaline myopathy","mesh","D017696"
< "3191","nemaline myopathy","umls","C0206157"
< "3191","nemaline myopathy","mondo","0018958"
< "0060009","MHC class I deficiency","mondo","0011476"
< "7465","chronic NK-cell lymphocytosis","umls","C1512709"
< "7465","chronic NK-cell lymphocytosis","mondo","0004234"
< "7848","interdigitating dendritic cell sarcoma","icd10cm","C96.4"
< "7848","interdigitating dendritic cell sarcoma","mesh","D054739"
< "7848","interdigitating dendritic cell sarcoma","umls","C1260326"
< "7848","interdigitating dendritic cell sarcoma","mondo","0005813"
---
> "13353","diffuse interstitial keratitis","icd10cm","H16.32"
> "13353","diffuse interstitial keratitis","icd9cm","370.52"
> "13353","diffuse interstitial keratitis","umls","C0155089"
> "13353","diffuse interstitial keratitis","mondo","0001694"
> "5632","optic nerve sheath meningioma","umls","C0346328"
> "5632","optic nerve sheath meningioma","mondo","0003557"
> "8481","rheumatic myocarditis","icd10cm","I01.9"
> "8481","rheumatic myocarditis","icd10cm","I09.0"
> "8481","rheumatic myocarditis","icd10cm","M05.3"
> "8481","rheumatic myocarditis","icd9cm","391.9"
> "8481","rheumatic myocarditis","icd9cm","398.0"
> "8481","rheumatic myocarditis","umls","C0035440"
> "8481","rheumatic myocarditis","umls","C0489959"
> "8481","rheumatic myocarditis","mondo","0004582"
> "8482","transient retinal arterial occlusion","icd10cm","H34.0"
> "8482","transient retinal arterial occlusion","icd9cm","362.34"
> "8482","transient retinal arterial occlusion","umls","C0154840"
> "8482","transient retinal arterial occlusion","mondo","0004583"
> "8483","retinal artery occlusion","mesh","D015356"
> "8483","retinal artery occlusion","umls","C0035302"
> "8483","retinal artery occlusion","mondo","0006948"
> "8484","maple bark strippers' lung","icd10cm","J67.6"
> "8484","maple bark strippers' lung","icd9cm","495.6"
> "8484","maple bark strippers' lung","umls","C0155890"
> "8484","maple bark strippers' lung","mondo","0004584"
> "8488","polyhydramnios","icd10cm","O40"
> "8488","polyhydramnios","icd9cm","657"
> "8488","polyhydramnios","icd9cm","657.0"
> "8488","polyhydramnios","mesh","D006831"
> "8488","polyhydramnios","umls","C0020224"
> "8488","polyhydramnios","mondo","0004585"
11918c25504
< "0110182","Charcot-Marie-Tooth disease axonal type 2C","omim","606071"
---
> "0070070","autosomal dominant non-syndromic intellectual disability 40","omim","616579"
11921c25507,25508
< "0070070","autosomal dominant non-syndromic intellectual disability 40","omim","616579"
---
> "1172","hyperlipoproteinemia type IV","omim","145750"
> "0110182","Charcot-Marie-Tooth disease axonal type 2C","omim","606071"
11923d25509
< "6678","tooth and nail syndrome","omim","189500"
11924a25511
> "0111344","myeloproliferative disorder with eosinophilia","omim","131440"
11927,11928c25514,25515
< "0110883","inflammatory bowel disease 17","omim","612261"
< "9273","citrullinemia","omim","605814"
---
> "0060793","hypomyelinating leukodystrophy 5","omim","610532"
> "0070176","spermatogenic failure 4","omim","270960"
11930d25516
< "0060556","Kufor-Rakeb syndrome","omim","606693"
11934,11936c25520,25523
< "0070188","spermatogenic failure 1","omim","258150"
< "0110039","Alzheimer's disease 7","omim","606187"
< "0110593","autosomal dominant nonsyndromic deafness 9","omim","601369"
---
> "4183","pseudopseudohypoparathyroidism","omim","612463"
> "4184","pseudohypoparathyroidism","omim","612462"
> "0050655","Bamforth-Lazarus syndrome","omim","241850"
> "0080136","multiple mitochondrial dysfunctions syndrome 4","omim","616370"
11941c25528,25529
< "0050167","autoimmune polyendocrine syndrome type 1","omim","240300"
---
> "0110851","rhizomelic chondrodysplasia punctata type 1","omim","215100"
> "1156","chondrocalcinosis","omim","118600"
11943,11945c25531,25537
< "0050425","restless legs syndrome","omim","610438"
< "0050425","restless legs syndrome","omim","610439"
< "0050747","lymphoplasmacytic lymphoma","omim","610430"
---
> "0111515","autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2","omim","616479"
> "0080061","autosomal recessive spinocerebellar ataxia 2","omim","213200"
> "0060827","X-linked intellectual disability-psychosis-macroorchidism syndrome","omim","300055"
> "0111249","uveal coloboma-cleft lip and palate-intellectual disability","omim","120433"
> "11975","coloboma of optic nerve","omim","120430"
> "0110964","brachydactyly type A1","omim","112500"
> "0080455","early infantile epileptic encephalopathy 52","omim","617350"
11946a25539
> "0050774","rapadilino syndrome","omim","266280"
11947a25541,25542
> "1757","facial hemiatrophy","omim","141300"
> "0111520","autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3","omim","609286"
11949c25544,25546
< "0060793","hypomyelinating leukodystrophy 5","omim","610532"
---
> "0080118","mitochondrial complex III deficiency nuclear type 9","omim","616111"
> "0090065","familial cold autoinflammatory syndrome 4","omim","616115"
> "13099","Moyamoya disease","omim","608796"
11952c25549,25550
< "0110955","Waardenburg syndrome type 4C","omim","613266"
---
> "0110254","cataract 25","omim","605728"
> "0110248","cataract 30","omim","116300"
11954d25551
< "0050588","muscular dystrophy-dystroglycanopathy","omim","613155"
11956,11957c25553,25554
< "0110615","primary ciliary dyskinesia 25","omim","615482"
< "0110545","autosomal dominant nonsyndromic deafness 13","omim","601868"
---
> "0050776","non-syndromic X-linked intellectual disability","omim","300498"
> "0060230","basal ganglia calcification","omim","615483"
11959c25556,25557
< "0060354","Stormorken syndrome","omim","185070"
---
> "3526","cerebral infarction","omim","601367"
> "0111285","psoriasis 11","omim","612599"
11962c25560,25561
< "0050786","iridogoniodysgenesis syndrome","omim","601631"
---
> "0050439","Usher syndrome","omim","276900"
> "12185","otosclerosis","omim","605727"
11964a25564
> "1324","lung cancer","omim","612593"
11968a25569
> "0060286","combined oxidative phosphorylation deficiency","omim","609060"
11970c25571,25572
< "0080019","metaphyseal dysplasia","omim","215050"
---
> "0111162","epidermal nevus","omim","162900"
> "12185","otosclerosis","omim","166800"
11971a25574
> "445","Bartter disease","omim","601678"
11974c25577,25580
< "0070131","autosomal dominant cutis laxa 3","omim","616603"
---
> "2211","factor XIII deficiency","omim","613235"
> "0080085","nonsyndromic congenital nail disorder 7","omim","605779"
> "0080246","Galloway-Mowat syndrome 4","omim","617730"
> "0080247","Galloway-Mowat syndrome 5","omim","617731"
11978a25585,25588
> "0080322","polycystic kidney disease","omim","173900"
> "1935","Bardet-Biedl syndrome","omim","209900"
> "0080588","agammaglobulinemia 5","omim","613506"
> "0110679","congenital myasthenic syndrome 4C","omim","608931"
11981a25592,25593
> "0080078","hypophosphatemic nephrolithiasis/osteoporosis 2","omim","612287"
> "0080077","hypophosphatemic nephrolithiasis/osteoporosis 1","omim","612286"
11986a25599
> "0111362","hawkinsinuria","omim","140350"
11988a25602,25603
> "10970","spastic quadriplegia","omim","612900"
> "0080589","Klippel-Feil syndrome 1","omim","118100"
11990,11991c25605,25608
< "14415","Legg-Calve-Perthes disease","omim","150600"
< "2962","Cockayne syndrome","omim","133540"
---
> "0070163","spermatogenic failure 21","omim","617644"
> "14757","type III Ehlers-Danlos syndrome","omim","130020"
> "0110080","Leber congenital amaurosis 12","omim","610612"
> "14735","hereditary angioedema","omim","610618"
11992a25610
> "0080110","multiple pterygium syndrome","omim","265000"
11993a25612
> "0060822","syndromic X-linked intellectual disability Cabezas type","omim","300354"
12000c25619,25620
< "0090053","episodic kinesigenic dyskinesia 1","omim","128200"
---
> "0060883","intestinal hypomagnesemia 1","omim","602014"
> "11459","pseudotumor cerebri","omim","243200"
12004a25625
> "0110591","autosomal dominant nonsyndromic deafness 7","omim","601412"
12005a25627
> "11555","Fuchs' endothelial dystrophy","omim","610158"
12007a25630,25631
> "0080384","nephrotic syndrome type 6","omim","614196"
> "0110897","inflammatory bowel disease 15","omim","612255"
12011,12012c25635,25637
< "0060481","Goldberg-Shprintzen syndrome","omim","609460"
< "0070202","familial partial lipodystrophy type 2","omim","151660"
---
> "0060280","primary pigmented nodular adrenocortical disease","omim","614190"
> "0111305","familial febrile seizures 4","omim","604352"
> "0110272","cataract 40","omim","302200"
12015a25641,25642
> "0080393","nephrotic syndrome type 18","omim","618177"
> "0080392","nephrotic syndrome type 17","omim","618176"
12020d25646
< "1657","ventricular septal defect","omim","614429"
12022,12023c25648,25653
< "0080052","acromesomelic dysplasia, Grebe type","omim","200700"
< "0050655","Bamforth-Lazarus syndrome","omim","241850"
---
> "0070188","spermatogenic failure 1","omim","258150"
> "0080394","nephrotic syndrome type 19","omim","618178"
> "0111566","familial isolated trichomegaly","omim","190330"
> "0050650","familial atrial fibrillation","omim","611494"
> "0110039","Alzheimer's disease 7","omim","606187"
> "0050680","Boomerang dysplasia","omim","112310"
12025c25655,25657
< "0110174","Charcot-Marie-Tooth disease axonal type 2L","omim","608673"
---
> "0070123","congenital nongoitrous hypothyroidism 4","omim","275100"
> "2960","photosensitive trichothiodystrophy","omim","601675"
> "0111579","asthma, nasal polyps, and aspirin intolerance","omim","208550"
12027a25660
> "0080046","Stickler syndrome","omim","184840"
12032c25665,25670
< "0110535","autosomal recessive nonsyndromic deafness 9","omim","601071"
---
> "0070043","autosomal dominant non-syndromic intellectual disability 13","omim","614563"
> "0111073","progressive familial heart block","omim","113900"
> "4990","essential tremor","omim","190300"
> "10488","imperforate anus","omim","207500"
> "0060454","subepithelial mucinous corneal dystrophy","omim","612867"
> "0070190","autosomal dominant chronic granulomatous disease","omim","138990"
12034a25673
> "14694","Johanson-Blizzard syndrome","omim","243800"
12036a25676
> "0080219","dystransthyretinemic hyperthyroxinemia","omim","145680"
12037a25678,25680
> "0060278","pontocerebellar hypoplasia type 9","omim","615809"
> "0111474","combined oxidative phosphorylation deficiency 1","omim","609060"
> "0111327","juvenile myoclonic epilepsy 4","omim","611364"
12038a25682,25683
> "0060279","pontocerebellar hypoplasia type 10","omim","615803"
> "0111512","metachondromatosis","omim","156250"
12040a25686
> "11996","spermatic cord torsion","omim","187400"
12043c25689
< "14264","benign neonatal seizures","omim","269720"
---
> "0070119","Meckel syndrome 5","omim","611561"
12048c25694
< "0080021","Schmid metaphyseal chondrodysplasia","omim","156500"
---
> "0060409","chromosome 1p32-p31 deletion syndrome","omim","613735"
12049a25696
> "0060842","isolated microphthalmia 3","omim","611038"
12051,12052c25698,25699
< "11830","myopia","omim","610320"
< "0110886","inflammatory bowel disease 9","omim","608448"
---
> "0110834","Usher syndrome type 1G","omim","606943"
> "0090049","paroxysmal nonkinesigenic dyskinesia 1","omim","118800"
12053a25701,25702
> "4346","variegate porphyria","omim","176200"
> "0060221","Maffucci syndrome","omim","614569"
12058,12059c25707,25709
< "0080316","megalencephalic leukoencephalopathy with subcortical cysts 1","omim","604004"
< "9074","systemic lupus erythematosus","omim","610065"
---
> "0070280","primary autosomal recessive microcephaly 5","omim","608716"
> "0110280","autosomal recessive limb-girdle muscular dystrophy type 2F","omim","601287"
> "0110429","dilated cardiomyopathy 1H","omim","604288"
12064,12067c25714,25720
< "0110180","Charcot-Marie-Tooth disease axonal type 2CC","omim","616924"
< "0060685","autosomal dominant nocturnal frontal lobe epilepsy 4","omim","610353"
< "0080351","CLOVES syndrome","omim","612918"
< "0110781","hereditary spastic paraplegia 30","omim","610357"
---
> "0080143","congenital fibrosis of the extraocular muscles","omim","602078"
> "0080389","nephrotic syndrome type 8","omim","615244"
> "0111354","arthrogryposis, renal dysfunction, and cholestasis 2","omim","613404"
> "0050881","inclusion body myopathy with Paget disease of bone and frontotemporal dementia","omim","167320"
> "13359","Ehlers-Danlos syndrome","omim","130000"
> "0070040","autosomal dominant non-syndromic intellectual disability 10","omim","614256"
> "0050529","adult spinal muscular atrophy","omim","271150"
12071,12072c25724,25727
< "0110445","dilated cardiomyopathy 1KK","omim","615248"
< "0050588","muscular dystrophy-dystroglycanopathy","omim","615249"
---
> "3659","sialuria","omim","269921"
> "9649","congenital nystagmus","omim","300814"
> "4795","GM2 gangliosidosis, AB variant","omim","272750"
> "0060381","orofaciodigital syndrome XI","omim","612913"
12074c25729
< "0060738","junctional epidermolysis bullosa non-Herlitz type","omim","226650"
---
> "0060288","omodysplasia","omim","164745"
12075a25731,25732
> "10611","protein-losing enteropathy","omim","226300"
> "0110519","autosomal recessive nonsyndromic deafness 68","omim","610419"
12077c25734
< "0060884","renal hypomagnesemia 6","omim","613882"
---
> "0060246","MASA syndrome","omim","303350"
12081a25739
> "0111283","psoriasis 3","omim","601454"
12085c25743,25745
< "1099","alpha thalassemia","omim","604131"
---
> "10283","prostate cancer","omim","611100"
> "0110006","3-methylglutaconic aciduria type 4","omim","250951"
> "0090145","dopamine beta-hydroxylase deficiency","omim","223360"
12088a25749
> "0080213","punctate palmoplantar keratoderma type II","omim","175860"
12090c25751
< "0110157","Charcot-Marie-Tooth disease type 2J","omim","607736"
---
> "0060245","Mast syndrome","omim","248900"
12092a25754
> "0110219","Brugada syndrome 2","omim","611777"
12096c25758,25759
< "0110651","long QT syndrome 10","omim","611819"
---
> "0050747","lymphoplasmacytic lymphoma","omim","610430"
> "0111438","optic atrophy 5","omim","610708"
12098a25762,25763
> "0111568","congenital vertical talus","omim","192950"
> "0080552","congenital disorder of glycosylation Ia","omim","212065"
12103,12104c25768,25774
< "13270","erythropoietic protoporphyria","omim","177000"
< "12177","common variable immunodeficiency","omim","607594"
---
> "5812","MHC class II deficiency","omim","209920"
> "0110486","autosomal recessive nonsyndromic deafness 28","omim","609823"
> "0110610","primary ciliary dyskinesia 34","omim","617091"
> "0060396","chromosome 15q25 deletion syndrome","omim","614294"
> "0060265","pontocerebellar hypoplasia type 1A","omim","607596"
> "13909","red-green color blindness","omim","303800"
> "0070253","congenital disorder of glycosylation type IIa","omim","212066"
12105a25776
> "0080533","Carney-Stratakis syndrome","omim","606864"
12107c25778,25781
< "0090015","Cenani-Lenz syndactyly syndrome","omim","212780"
---
> "10584","retinitis pigmentosa","omim","268000"
> "10283","prostate cancer","omim","610997"
> "0080134","multiple mitochondrial dysfunctions syndrome 2","omim","614299"
> "0050956","spinocerebellar ataxia type 6","omim","183086"
12109c25783
< "2058","chronic mucocutaneous candidiasis","omim","613956"
---
> "0110503","autosomal recessive nonsyndromic deafness 46","omim","609647"
12120c25794
< "14365","systemic primary carnitine deficiency disease","omim","212140"
---
> "0111156","spermatogenic failure 9","omim","613958"
12122c25796,25798
< "14450","46 XX gonadal dysgenesis","omim","233300"
---
> "14448","46 XY gonadal dysgenesis","omim","233420"
> "0090067","Fuhrmann syndrome","omim","228930"
> "0110966","brachydactyly type A3","omim","112700"
12123a25800
> "11830","myopia","omim","610320"
12126a25804
> "0090055","dystonia 25","omim","615073"
12128,12129c25806,25810
< "0110338","osteogenesis imperfecta type 17","omim","616507"
< "0110667","congenital myasthenic syndrome 5","omim","603034"
---
> "0080422","Dravet syndrome","omim","607208"
> "0090117","thiamine-responsive megaloblastic anemia syndrome","omim","249270"
> "0090073","hypogonadotropic hypogonadism 13 with or without anosmia","omim","614842"
> "0110240","cataract 20 multiple types","omim","116100"
> "0111194","autosomal dominant adult-onset proximal spinal muscular atrophy","omim","182980"
12130a25812
> "0110518","autosomal recessive nonsyndromic deafness 67","omim","610265"
12132c25814,25815
< "0070089","schizophrenia 13","omim","613025"
---
> "0050799","guanidinoacetate methyltransferase deficiency","omim","612736"
> "83","cataract","omim","116200"
12133a25817,25818
> "0111313","idiopathic generalized epilepsy 12","omim","614847"
> "0060427","chromosome Xp21 deletion syndrome","omim","300679"
12134a25820,25821
> "14711","FG syndrome","omim","300581"
> "0111554","spondylometaphyseal dysplasia Kozlowski type","omim","184252"
12136a25824,25825
> "0111245","palmoplantar keratoderma and congenital alopecia 2","omim","212360"
> "0080360","fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4","omim","616501"
12137a25827,25828
> "1657","ventricular septal defect","omim","614431"
> "0110158","Charcot-Marie-Tooth disease type 2I","omim","607677"
12138a25830,25831
> "0111243","acromicric dysplasia","omim","102370"
> "0111542","familial expansile osteolysis","omim","174810"
12139a25833
> "0050489","multinodular goiter","omim","606082"
12141d25834
< "0050675","Birk-Barel syndrome","omim","612292"
12142a25836,25837
> "0080065","autosomal recessive spinocerebellar ataxia 19","omim","616291"
> "0060438","Cole-Carpenter syndrome","omim","616294"
12144,12145c25839,25841
< "0060706","X-linked lymphoproliferative syndrome 2","omim","300635"
< "3369","Ewing sarcoma","omim","612219"
---
> "0110490","autosomal recessive nonsyndromic deafness 31","omim","607084"
> "0110779","hereditary spastic paraplegia 28","omim","609340"
> "14004","thoracic aortic aneurysm","omim","607087"
12147c25843
< "0080082","nonsyndromic congenital nail disorder 4","omim","206800"
---
> "0060266","pontocerebellar hypoplasia type 1B","omim","614678"
12152,12153c25848,25851
< "0110588","autosomal dominant nonsyndromic deafness 67","omim","616340"
< "2987","familial Mediterranean fever","omim","249100"
---
> "0080437","early infantile epileptic encephalopathy 31","omim","616346"
> "0060430","chromosome 16p11.2 duplication syndrome","omim","614671"
> "0110311","hypertrophic cardiomyopathy 21","omim","614676"
> "0080465","early infantile epileptic encephalopathy 30","omim","616341"
12156a25855,25856
> "0111412","exudative vitreoretinopathy 1","omim","133780"
> "5572","Beckwith-Wiedemann syndrome","omim","130650"
12158c25858,25860
< "0050776","non-syndromic X-linked intellectual disability","omim","300498"
---
> "0110278","autosomal recessive limb-girdle muscular dystrophy type 2D","omim","608099"
> "0090007","immunodeficiency-centromeric instability-facial anomalies syndrome","omim","242860"
> "893","Wilson disease","omim","277900"
12161c25863,25865
< "0060230","basal ganglia calcification","omim","615483"
---
> "0110545","autosomal dominant nonsyndromic deafness 13","omim","601868"
> "0050677","Bjornstad syndrome","omim","262000"
> "0110646","long QT syndrome 3","omim","603830"
12163a25868
> "0060261","congenital ptosis","omim","300245"
12165,12166c25870,25875
< "0110628","primary ciliary dyskinesia 24","omim","615481"
< "11830","myopia","omim","608908"
---
> "0080110","multiple pterygium syndrome","omim","178110"
> "9574","choanal atresia","omim","608911"
> "0111556","steatocystoma multiplex","omim","184500"
> "1837","diabetic ketoacidosis","omim","612227"
> "0060272","pontocerebellar hypoplasia type 3","omim","608027"
> "0080311","X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance","omim","300486"
12168c25877
< "628","combined T cell and B cell immunodeficiency","omim","312863"
---
> "0060378","orofaciodigital syndrome VIII","omim","300484"
12170c25879
< "1094","attention deficit hyperactivity disorder","omim","608904"
---
> "6688","autoimmune lymphoproliferative syndrome","omim","601859"
12172c25881
< "13636","Fanconi anemia","omim","227650"
---
> "1094","attention deficit hyperactivity disorder","omim","608906"
12175a25885
> "0111211","distal spinal muscular atrophy type 3","omim","607088"
12178a25889
> "0111480","combined oxidative phosphorylation deficiency 10","omim","614702"
12181c25892
< "0110023","age related macular degeneration 11","omim","611953"
---
> "0080508","Cornelia de Lange syndrome 4","omim","614701"
12186c25897,25900
< "0110912","leukocyte adhesion deficiency 3","omim","612840"
---
> "0111447","progressive myoclonus epilepsy 7","omim","616187"
> "0111229","congenital muscular dystrophy-dystroglycanopathy type A","omim","236670"
> "0110201","Charcot-Marie-Tooth disease recessive intermediate A","omim","608340"
> "0090087","hypogonadotropic hypogonadism 14 with or without anosmia","omim","614858"
12188c25902
< "0110342","osteogenesis imperfecta type 13","omim","614856"
---
> "0060879","primary hypomagnesemia","omim","602014"
12191,12192c25905,25907
< "14744","Partington syndrome","omim","309510"
< "0070011","Seckel syndrome 7","omim","614851"
---
> "0110547","autosomal dominant nonsyndromic deafness 16","omim","603964"
> "0111129","focal segmental glomerulosclerosis 2","omim","603965"
> "0080245","Galloway-Mowat syndrome 3","omim","617729"
12193a25909
> "0111212","distal hereditary motor neuronopathy type 9","omim","617721"
12194a25911,25913
> "0111441","optic atrophy 1","omim","165500"
> "5409","lung small cell carcinoma","omim","182280"
> "0050947","hereditary hypophosphatemic rickets with hypercalciuria","omim","241530"
12197c25916,25917
< "4997","Camurati-Engelmann disease","omim","131300"
---
> "0050593","primary congenital glaucoma","omim","613085"
> "0050593","primary congenital glaucoma","omim","613086"
12198a25919,25921
> "0060283","peeling skin syndrome","omim","613088"
> "0110359","retinitis pigmentosa 67","omim","615565"
> "0111266","geroderma osteodysplasticum","omim","231070"
12202c25925,25928
< "0110379","retinitis pigmentosa 43","omim","613810"
---
> "0110067","juvenile amyotrophic lateral sclerosis with dementia","omim","205200"
> "0110865","congenital stationary night blindness 1B","omim","257270"
> "0060267","pontocerebellar hypoplasia type 2A","omim","277470"
> "0110538","autosomal recessive nonsyndromic deafness 96","omim","614414"
12204a25931,25932
> "3138","acanthosis nigricans","omim","200170"
> "13724","scurvy","omim","240400"
12205a25934
> "0080059","autosomal recessive spinocerebellar ataxia 7","omim","609270"
12207,12208c25936,25942
< "0110935","nemaline myopathy 6","omim","609273"
< "0110116","autoimmune lymphoproliferative syndrome type 2B","omim","607271"
---
> "0050568","spondylocostal dysostosis","omim","122600"
> "12271","aniridia","omim","106210"
> "10892","hypospadias","omim","300633"
> "0080263","autosomal recessive nonsyndromic deafness 108","omim","617654"
> "0110231","cataract 1 multiple types","omim","116200"
> "2729","dyskeratosis congenita","omim","127550"
> "0111590","Cohen syndrome","omim","216550"
12209a25944,25945
> "0111553","spondyloepiphyseal dysplasia Maroteaux type","omim","184095"
> "0111154","postural orthostatic tachycardia syndrome","omim","604715"
12211,12213c25947,25950
< "0110219","Brugada syndrome 2","omim","611777"
< "0110577","autosomal dominant nonsyndromic deafness 51","omim","613558"
< "3052","Balkan nephropathy","omim","124100"
---
> "0060601","alpha-2-plasmin inhibitor deficiency","omim","262850"
> "0080379","nephrotic syndrome type 2","omim","600995"
> "0111487","combined oxidative phosphorylation deficiency 7","omim","613559"
> "11782","astigmatism","omim","603047"
12216a25954
> "0080087","nonsyndromic congenital nail disorder 9","omim","614149"
12218a25957
> "0080194","Carey-Fineman-Ziter syndrome","omim","254940"
12222a25962,25963
> "0110608","primary ciliary dyskinesia 19","omim","614935"
> "705","Leber hereditary optic neuropathy","omim","535000"
12224c25965
< "0110973","Mononen-Karnes-Senac syndrome","omim","301940"
---
> "0070012","Seckel syndrome 5","omim","613823"
12225a25967,25968
> "0111378","fetal akinesia deformation sequence syndrome 2","omim","618388"
> "0111376","fetal akinesia deformation sequence syndrome 3","omim","618389"
12228a25972
> "0111225","centronuclear myopathy X-linked","omim","310400"
12231c25975
< "0111055","platelet-type bleeding disorder 20","omim","616913"
---
> "0080032","craniodiaphyseal dysplasia","omim","218300"
12234,12235c25978,25983
< "0110550","autosomal dominant nonsyndromic deafness 20","omim","604717"
< "12177","common variable immunodeficiency","omim","613496"
---
> "0070177","spermatogenic failure 22","omim","617706"
> "0080401","orofacial cleft 8","omim","618149"
> "0060360","hereditary papulotranslucent acrokeratoderma","omim","101840"
> "0110124","Bardet-Biedl syndrome 2","omim","615981"
> "0111565","trichodontoosseous syndrome","omim","190320"
> "0110258","cataract 10 multiple types","omim","600881"
12236a25985
> "0050949","autosomal recessive hypophosphatemic rickets","omim","241520"
12239a25989,25990
> "0110509","autosomal recessive nonsyndromic deafness 53","omim","609706"
> "0080041","hypochondroplasia","omim","146000"
12241c25992
< "0070183","spermatogenic failure 5","omim","243060"
---
> "0050954","spinocerebellar ataxia type 1","omim","164400"
12242a25994
> "9970","obesity","omim","601665"
12249a26002
> "0111272","occipital horn syndrome","omim","304150"
12250a26004
> "0060704","lymphoproliferative syndrome","omim","308240"
12252c26006
< "0110591","autosomal dominant nonsyndromic deafness 7","omim","601412"
---
> "0080405","orofacial cleft 12","omim","612858"
12254,12255c26008,26010
< "8986","narcolepsy","omim","612851"
< "0050425","restless legs syndrome","omim","612853"
---
> "0080135","multiple mitochondrial dysfunctions syndrome 3","omim","615330"
> "0050648","atelosteogenesis","omim","108720"
> "0050648","atelosteogenesis","omim","108721"
12260c26015,26016
< "12801","mucopolysaccharidosis III","omim","252930"
---
> "0111393","mucopolysaccharidosis type IIIC","omim","252930"
> "0111340","dominant optic atrophy plus syndrome","omim","125250"
12262c26018
< "0110238","cataract 18","omim","610019"
---
> "2908","Treacher Collins syndrome","omim","613717"
12264c26020
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","615817"
---
> "0050942","spastic ataxia 3","omim","611390"
12265a26022,26023
> "0111287","psoriasis 13","omim","614070"
> "0060541","Hermansky-Pudlak syndrome 3","omim","614072"
12266a26025
> "0060543","Hermansky-Pudlak syndrome 5","omim","614074"
12268c26027,26028
< "0110185","Charcot-Marie-Tooth disease type 4A","omim","214400"
---
> "0050588","muscular dystrophy-dystroglycanopathy","omim","613155"
> "0060546","Hermansky-Pudlak syndrome 8","omim","614077"
12270a26031,26033
> "0080561","congenital disorder of glycosylation Ii","omim","607906"
> "3507","dermatofibrosarcoma protuberans","omim","607907"
> "0080421","early infantile epileptic encephalopathy 11","omim","613721"
12273c26036,26037
< "0110703","hypotrichosis 6","omim","607903"
---
> "0080459","early infantile epileptic encephalopathy 12","omim","613722"
> "0110422","autosomal recessive pericentral pigmentary retinopathy","omim","268060"
12275c26039,26040
< "14791","Leber congenital amaurosis","omim","204000"
---
> "0080558","congenital disorder of glycosylation If","omim","609180"
> "0050473","Alstrom syndrome","omim","203800"
12280a26046,26047
> "5339","cyclic hematopoiesis","omim","162800"
> "0050432","Asperger syndrome","omim","608631"
12284c26051,26052
< "0080422","Dravet syndrome","omim","607208"
---
> "0060461","chromosome Xp11.23-p11.22 duplication syndrome","omim","300801"
> "0111207","distal hereditary motor neuropathy type 2B","omim","608634"
12285a26054,26055
> "0050432","Asperger syndrome","omim","608638"
> "0060563","Char syndrome","omim","169100"
12288,12289c26058,26059
< "0110629","Wolfram syndrome 1","omim","222300"
< "3012","Li-Fraumeni syndrome","omim","151623"
---
> "0110331","Leber congenital amaurosis 3","omim","604232"
> "0111503","Li-Fraumeni syndrome 1","omim","151623"
12291a26062
> "0080294","Charcot-Marie-Tooth disease dominant intermediate G","omim","617882"
12292a26064
> "0111370","apolipoprotein C-III deficiency","omim","614028"
12296,12297c26068,26069
< "0110374","retinitis pigmentosa 68","omim","615725"
< "2106","myotonia congenita","omim","255700"
---
> "2065","syringoma","omim","186600"
> "10908","hydrocephalus","omim","307000"
12299,12301c26071,26075
< "0110546","autosomal dominant nonsyndromic deafness 15","omim","602459"
< "0070029","ITM2B-related cerebral amyloid angiopathy 1","omim","176500"
< "2580","rhizomelic chondrodysplasia punctata","omim","215100"
---
> "0060851","pemphigus vulgaris","omim","169610"
> "0050968","autosomal dominant cerebellar ataxia, deafness and narcolepsy","omim","604121"
> "0060472","Kindler syndrome","omim","173650"
> "0110844","xeroderma pigmentosum group C","omim","278720"
> "0080549","LEOPARD syndrome 2","omim","611554"
12305a26080
> "0111323","idiopathic generalized epilepsy 9","omim","607682"
12308a26084,26086
> "0111298","familial febrile seizures 8","omim","607681"
> "0111304","familial febrile seizures 10","omim","612637"
> "583","hemolytic anemia","omim","612631"
12309a26088,26089
> "0050955","spinocerebellar ataxia type 2","omim","183090"
> "0110433","dilated cardiomyopathy 1E","omim","601154"
12312c26092,26096
< "8552","chronic myeloid leukemia","omim","608232"
---
> "0080519","PAPA syndrome","omim","604416"
> "14448","46 XY gonadal dysgenesis","omim","616067"
> "0080555","congenital disorder of glycosylation Ic","omim","603147"
> "0050908","myelodysplastic syndrome","omim","614286"
> "0060410","chromosome 1p36 deletion syndrome","omim","607872"
12313a26098
> "2247","spondylosis","omim","184300"
12315c26100,26101
< "10487","Hirschsprung's disease","omim","606874"
---
> "0110813","hereditary spastic paraplegia 62","omim","615681"
> "0060256","Dowling-Degos disease","omim","615327"
12320c26106
< "0110815","hereditary spastic paraplegia 64","omim","615683"
---
> "0060287","cornea plana","omim","217300"
12321a26108,26110
> "0111514","metatropic dysplasia","omim","156530"
> "0090089","hypogonadotropic hypogonadism 10 with or without anosmia","omim","614839"
> "4428","dyslexia","omim","606896"
12324a26114,26116
> "0111439","optic atrophy 8","omim","616648"
> "13774","Addison's disease","omim","103230"
> "0080414","early infantile epileptic encephalopathy 15","omim","615006"
12329,12331c26121,26125
< "1040","chronic lymphocytic leukemia","omim","609630"
< "0070278","primary autosomal recessive microcephaly 7","omim","612703"
< "0111102","maturity-onset diabetes of the young type 3","omim","600496"
---
> "1932","Angelman syndrome","omim","105830"
> "0111074","progressive familial heart block type IA","omim","113900"
> "0090086","hypogonadotropic hypogonadism 6 with or without anosmia","omim","612702"
> "1040","chronic lymphocytic leukemia","omim","151400"
> "0110273","autosomal dominant limb-girdle muscular dystrophy","omim","603511"
12332a26127,26128
> "13809","familial combined hyperlipidemia","omim","144250"
> "0111401","congenital dyserythropoietic anemia type II","omim","224100"
12334c26130,26132
< "0110400","retinitis pigmentosa 22","omim","602594"
---
> "14681","Silver-Russell syndrome","omim","180860"
> "0080335","mitochondrial DNA depletion syndrome 12b","omim","615418"
> "0080293","short-rib thoracic dysplasia 18 with polydactyly","omim","617866"
12336a26135,26138
> "0060334","transient neonatal diabetes mellitus","omim","610374"
> "0111183","familial hemiplegic migraine 3","omim","609634"
> "1056","oculocerebrorenal syndrome","omim","309000"
> "1702","ichthyosis vulgaris","omim","146700"
12338c26140,26143
< "0110222","Brugada syndrome 5","omim","612838"
---
> "0111219","Friedreich ataxia 2","omim","601992"
> "0111427","restrictive cardiomyopathy 3","omim","612422"
> "0110043","Alzheimer's disease 10","omim","609636"
> "0060581","Noonan syndrome 3","omim","609942"
12339a26145,26146
> "0111442","optic atrophy 9","omim","616289"
> "0060299","complement component 6 deficiency","omim","612446"
12342d26148
< "0070145","hereditary sensory and autonomic neuropathy type 5","omim","608654"
12343a26150,26151
> "0080079","nonsyndromic congenital nail disorder 1","omim","161050"
> "0111248","cerebrocostomandibular syndrome","omim","117650"
12346a26155,26157
> "0050787","juvenile polyposis syndrome","omim","174900"
> "0090085","hypogonadotropic hypogonadism 9 with or without anosmia","omim","614838"
> "4297","scimitar syndrome","omim","106700"
12347a26159
> "12376","juvenile spinal muscular atrophy","omim","253400"
12353c26165,26166
< "0060230","basal ganglia calcification","omim","606656"
---
> "0090071","hypogonadotropic hypogonadism 11 with or without anosmia","omim","614840"
> "14501","Sjogren-Larsson syndrome","omim","270200"
12356c26169
< "0090140","cortisone reductase deficiency 2","omim","614662"
---
> "0050965","spinocerebellar ataxia type 15","omim","606658"
12359a26173
> "0080066","autosomal recessive spinocerebellar ataxia 20","omim","616354"
12360a26175,26177
> "0080553","congenital disorder of glycosylation Iaa","omim","617082"
> "0111188","myofibrillar myopathy 9","omim","603689"
> "0080444","early infantile epileptic encephalopathy 27","omim","616139"
12362,12365c26179,26185
< "0110030","alpha thalassemia-X-linked intellectual disability syndrome","omim","301040"
< "0110910","leukocyte adhesion deficiency 1","omim","116920"
< "9870","galactosemia","omim","230400"
< "0111101","maturity-onset diabetes of the young type 5","omim","137920"
---
> "0080197","congenital muscular dystrophy with cataracts and intellectual disability","omim","617404"
> "0080068","Charcot-Marie-Tooth disease type 6","omim","601152"
> "12308","Dubin-Johnson syndrome","omim","237500"
> "1858","McCune Albright syndrome","omim","174800"
> "0111397","congenital dyserythropoietic anemia type Ib","omim","615631"
> "0111459","classic galactosemia","omim","230400"
> "10871","age related macular degeneration","omim","603075"
12366a26187
> "0050489","multinodular goiter","omim","300273"
12368c26189,26190
< "2352","hemochromatosis","omim","231100"
---
> "0070084","schizophrenia 8","omim","603206"
> "0110237","cataract 42","omim","115900"
12370,12371c26192,26193
< "0110662","congenital myasthenic syndrome 1B","omim","608930"
< "0110679","congenital myasthenic syndrome 4C","omim","608931"
---
> "0111007","X-linked cone-rod dystrophy 3","omim","300476"
> "0080317","megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation","omim","613926"
12373a26196
> "1324","lung cancer","omim","608935"
12374a26198
> "0111547","retinal arterial tortuosity","omim","180000"
12377a26202
> "1148","polydactyly","omim","603596"
12379a26205
> "0110222","Brugada syndrome 5","omim","612838"
12385c26211,26212
< "0111054","von Willebrand's disease 3","omim","277480"
---
> "0111259","postaxial acrofacial dysostosis","omim","263750"
> "0111085","Fanconi anemia complementation group U","omim","617247"
12390,12391c26217,26218
< "0070000","3-methylglutaconic aciduria type VIII","omim","617248"
< "1929","supravalvular aortic stenosis","omim","185500"
---
> "0070000","3-methylglutaconic aciduria type 8","omim","617248"
> "0110590","autosomal dominant nonsyndromic deafness 69","omim","616697"
12394a26222
> "0060455","Thiel-Behnke corneal dystrophy","omim","602082"
12396a26225
> "0111275","speech-language disorder-1","omim","602081"
12398a26228
> "13543","hyperparathyroidism","omim","145000"
12401,12402c26231,26234
< "0050535","exudative vitreoretinopathy","omim","605750"
< "0110156","Charcot-Marie-Tooth disease type 2B1","omim","605588"
---
> "0111409","exudative vitreoretinopathy 3","omim","605750"
> "0111079","birdshot chorioretinopathy","omim","605808"
> "2120","focal dermal hypoplasia","omim","305600"
> "14699","thrombocytopenia-absent radius syndrome","omim","274000"
12404a26237,26238
> "0111220","centronuclear myopathy 2","omim","255200"
> "0080590","Klippel-Feil syndrome 2","omim","214300"
12405a26240
> "0111518","autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5","omim","613077"
12407c26242
< "0110859","polycystic kidney disease 2","omim","613095"
---
> "0060468","Holt-Oram syndrome","omim","142900"
12409a26245
> "0060062","familial juvenile hyperuricemic nephropathy","omim","613092"
12411c26247
< "0110146","Bartter disease type 4b","omim","613090"
---
> "0080330","cold-induced sweating syndrome 2","omim","610313"
12413,12414c26249,26254
< "0110525","autosomal recessive nonsyndromic deafness 77","omim","613079"
< "0060898","early-onset Parkinson's disease 20","omim","615530"
---
> "0060258","reticulate acropigmentation of Kitamura","omim","615537"
> "9649","congenital nystagmus","omim","300589"
> "0110282","autosomal recessive limb-girdle muscular dystrophy type 2H","omim","254110"
> "0060898","Parkinson's disease 20","omim","615530"
> "0110185","Charcot-Marie-Tooth disease type 4A","omim","214400"
> "0110975","brachydactyly type B2","omim","611377"
12416c26256,26257
< "14711","FG syndrome","omim","300581"
---
> "0111226","X-linked congenital myopathy with fiber-type disproportion","omim","300580"
> "0060387","chondrodysplasia Blomstrand type","omim","215045"
12418c26259,26261
< "0110340","osteogenesis imperfecta type 4","omim","166220"
---
> "0080264","exudative vitreoretinopathy 7","omim","617572"
> "0060437","chromosome 22q13 duplication syndrome","omim","615538"
> "0060571","Ritscher-Schinzel syndrome 1","omim","220210"
12422d26264
< "0070253","congenital disorder of glycosylation type IIa","omim","212066"
12425c26267,26273
< "0050681","Borjeson-Forssman-Lehmann syndrome","omim","301900"
---
> "1388","Tangier disease","omim","205400"
> "0080269","autosomal dominant nonsyndromic deafness 73","omim","617663"
> "0111492","combined oxidative phosphorylation deficiency 32","omim","617664"
> "0080282","early infantile epileptic encephalopathy 56","omim","617665"
> "0111407","Fraser syndrome 2","omim","617666"
> "0111406","Fraser syndrome 3","omim","617667"
> "2581","chondrodysplasia punctata","omim","215105"
12427,12428c26275,26277
< "0050763","ARC syndrome","omim","208085"
< "0060827","X-linked intellectual disability-psychosis-macroorchidism syndrome","omim","300055"
---
> "0050167","autoimmune polyendocrine syndrome type 1","omim","240300"
> "0080110","multiple pterygium syndrome","omim","253290"
> "0080418","early infantile epileptic encephalopathy 54","omim","617391"
12430,12431c26279,26280
< "0050797","peroxisomal acyl-CoA oxidase deficiency","omim","264470"
< "4465","papillary renal cell carcinoma","omim","605074"
---
> "0110024","age related macular degeneration 12","omim","613784"
> "0070269","congenital disorder of glycosylation type IIq","omim","617395"
12432a26282
> "0060423","chromosome 6q11-q14 deletion syndrome","omim","613544"
12433a26284
> "0110395","retinitis pigmentosa 72","omim","616469"
12434a26286,26288
> "0111250","Parkinson's disease 3","omim","602404"
> "14004","thoracic aortic aneurysm","omim","613780"
> "0111403","mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations","omim","618273"
12438c26292
< "0050650","familial atrial fibrillation","omim","611494"
---
> "0050946","Charlevoix-Saguenay spastic ataxia","omim","270550"
12442c26296,26301
< "0050763","ARC syndrome","omim","613404"
---
> "0111475","combined oxidative phosphorylation deficiency 39","omim","618397"
> "0111470","combined oxidative phosphorylation deficiency 28","omim","616794"
> "0111379","fetal akinesia deformation sequence syndrome 4","omim","618393"
> "0111521","autosomal dominant progressive external ophthalmoplegia 1","omim","157640"
> "0111573","autosomal dominant woolly hair","omim","194300"
> "0110180","Charcot-Marie-Tooth disease axonal type 2CC","omim","616924"
12445c26304,26305
< "0110006","3-methylglutaconic aciduria type 4","omim","250951"
---
> "1024","leprosy","omim","613407"
> "0080457","microcephaly, seizures, and developmental delay","omim","613402"
12448a26309
> "0111506","palmoplantar keratoderma-esophageal carcinoma syndrome","omim","148500"
12453c26314
< "0110240","cataract 20 multiple types","omim","116100"
---
> "0080043","achondrogenesis","omim","200600"
12455,12456c26316,26318
< "1442","Alpers syndrome","omim","203700"
< "1338","congenital dyserythropoietic anemia","omim","105600"
---
> "0080062","autosomal recessive spinocerebellar ataxia 13","omim","614831"
> "0080122","mitochondrial DNA depletion syndrome 4a","omim","203700"
> "0111399","congenital dyserythropoietic anemia type III","omim","105600"
12458,12460c26320,26325
< "0110155","Charcot-Marie-Tooth disease type 2A2","omim","609260"
< "0050631","Allan-Herndon-Dudley syndrome","omim","300523"
< "0050535","exudative vitreoretinopathy","omim","133780"
---
> "0110155","Charcot-Marie-Tooth disease type 2A2A","omim","609260"
> "0111537","paroxysmal extreme pain disorder","omim","167400"
> "0070254","congenital disorder of glycosylation type IIb","omim","606056"
> "0070229","intrahepatic cholestasis of pregnancy 3","omim","614972"
> "0080116","mitochondrial complex III deficiency nuclear type 7","omim","615824"
> "0111527","spinal muscular atrophy with progressive myoclonic epilepsy","omim","159950"
12462,12464c26327,26331
< "0060886","osteopathia striata with cranial sclerosis","omim","300373"
< "0110702","hypotrichosis 5","omim","612841"
< "0080143","congenital fibrosis of the extraocular muscles","omim","602078"
---
> "0080472","infantile or early childhood epileptic encephalopathy 1","omim","617711"
> "3393","coronary artery disease","omim","612030"
> "0111469","combined oxidative phosphorylation deficiency 16","omim","615395"
> "0080140","multiple congenital anomalies-hypotonia-seizures syndrome 3","omim","615398"
> "0060284","paroxysmal nocturnal hemoglobinuria","omim","615399"
12466,12467c26333,26337
< "0070055","Xia-Gibbs Syndrome","omim","615829"
< "12801","mucopolysaccharidosis III","omim","252940"
---
> "0060674","catecholaminergic polymorphic ventricular tachycardia","omim","604772"
> "0111349","hereditary desmoid disease","omim","135290"
> "0110529","autosomal recessive nonsyndromic deafness 84A","omim","613391"
> "0111402","mucopolysaccharidosis type IIID","omim","252940"
> "0111433","optic atrophy 3","omim","165300"
12468a26339
> "0080056","achondrogenesis type II","omim","200610"
12473c26344
< "0110077","arrhythmogenic right ventricular dysplasia 9","omim","609040"
---
> "9146","visceral leishmaniasis","omim","611382"
12475,12476c26346,26348
< "0050811","congenital adrenal hyperplasia","omim","202110"
< "12308","Dubin-Johnson syndrome","omim","237500"
---
> "0050794","multiple synostoses syndrome","omim","610017"
> "0050958","spinocerebellar ataxia type 7","omim","164500"
> "2987","familial Mediterranean fever","omim","134610"
12481c26353,26354
< "0110270","cataract 17 multiple types","omim","611544"
---
> "0111190","distal muscular dystrophy 4","omim","614065"
> "0060240","UV-sensitive syndrome","omim","600630"
12483c26356,26357
< "0070152","hereditary sensory and autonomic neuropathy type 1A","omim","162400"
---
> "0080033","craniometaphyseal dysplasia","omim","218400"
> "5394","prolactinoma","omim","600634"
12490c26364
< "14717","centronuclear myopathy","omim","310400"
---
> "2106","myotonia congenita","omim","255700"
12494c26368,26369
< "0060383","acrofacial dysostosis Rodriguez type","omim","201170"
---
> "1339","Diamond-Blackfan anemia","omim","612563"
> "0050779","hydrolethalus syndrome","omim","236680"
12497a26373,26374
> "12120","pulmonary alveolar proteinosis","omim","614370"
> "0090120","hereditary neutrophilia","omim","162830"
12500,12501c26377,26380
< "0110047","Alzheimer's disease 14","omim","611154"
< "14766","renal agenesis","omim","191830"
---
> "0111234","congenital muscular dystrophy-dystroglycanopathy A7","omim","614643"
> "0111102","maturity-onset diabetes of the young type 3","omim","600496"
> "0080296","hypomyelinating leukodystrophy 14","omim","617899"
> "12185","otosclerosis","omim","608484"
12503c26382
< "0110048","Alzheimer's disease 15","omim","611155"
---
> "0110114","atrial heart septal defect 9","omim","614475"
12505a26385
> "0080295","short-rib thoracic dysplasia 19 with or without polydactyly","omim","617895"
12507a26388,26389
> "0060695","hyperekplexia","omim","149400"
> "12185","otosclerosis","omim","612096"
12509a26392,26393
> "1148","polydactyly","omim","174200"
> "0080582","hypotrichosis 14","omim","618275"
12510a26395
> "14291","LEOPARD syndrome","omim","151100"
12512a26398
> "0110681","congenital myasthenic syndrome 2A","omim","616313"
12517c26403
< "10126","keratoconus","omim","614623"
---
> "3320","Tay-Sachs disease","omim","272800"
12518a26405,26407
> "0050770","polycystic liver disease","omim","174050"
> "13270","erythropoietic protoporphyria","omim","177000"
> "8161","thyroid gland Hurthle cell carcinoma","omim","607464"
12522,12523c26411,26414
< "0111162","epidermal nevus","omim","162900"
< "0110114","atrial heart septal defect 9","omim","614475"
---
> "0060397","chromosome 15q26-qter deletion syndrome","omim","612626"
> "2861","congenital nonspherocytic hemolytic anemia","omim","300908"
> "0050651","atrioventricular septal defect","omim","614474"
> "0110048","Alzheimer's disease 15","omim","611155"
12524a26416
> "0110117","autoimmune lymphoproliferative syndrome type 4","omim","614470"
12526a26419
> "327","syringomyelia","omim","186700"
12528,12529c26421,26422
< "0060888","transient myeloproliferative syndrome","omim","159595"
< "0111115","nephronophthisis 4","omim","606966"
---
> "10126","keratoconus","omim","614629"
> "0070093","schizophrenia 18","omim","615232"
12532a26426
> "0080583","Wolfram syndrome, mitochondrial form","omim","598500"
12535,12536c26429,26431
< "9273","citrullinemia","omim","215700"
< "0110723","neuronal ceroid lipofuscinosis 8","omim","600143"
---
> "11721","glycogen storage disease VII","omim","232800"
> "0111357","adermatoglyphia","omim","136000"
> "0050857","Perrault syndrome","omim","233400"
12538a26434,26435
> "0060488","Pitt-Hopkins syndrome","omim","610954"
> "0110342","osteogenesis imperfecta type 13","omim","614856"
12542c26439
< "0110721","neuronal ceroid lipofuscinosis 1","omim","256730"
---
> "0050629","Aicardi-Goutieres syndrome","omim","615010"
12544a26442,26443
> "0080113","mitochondrial complex III deficiency nuclear type 4","omim","615159"
> "0110598","primary ciliary dyskinesia 14","omim","613807"
12548,12549c26447,26448
< "0050540","Charcot-Marie-Tooth disease type 3","omim","145900"
< "0060829","Brooks-Wisniewski-Brown syndrome","omim","300612"
---
> "0050712","AGAT deficiency","omim","612718"
> "11830","myopia","omim","612717"
12551c26450
< "0110482","autosomal recessive nonsyndromic deafness 24","omim","611022"
---
> "0060304","dyschromatosis universalis hereditaria","omim","612715"
12552a26452
> "0050807","Kahrizi syndrome","omim","612713"
12555a26456
> "0110615","primary ciliary dyskinesia 25","omim","615482"
12557c26458
< "0111163","molybdenum cofactor deficiency type B","omim","252160"
---
> "0080292","retinitis pigmentosa 81","omim","617871"
12558a26460,26463
> "0111464","combined oxidative phosphorylation deficiency 35","omim","617873"
> "0111497","combined oxidative phosphorylation deficiency 34","omim","617872"
> "0111539","parastremmatic dwarfism","omim","168400"
> "0060297","complement component 4a deficiency","omim","614380"
12564,12566c26469,26472
< "0070266","congenital disorder of glycosylation type IIn","omim","616721"
< "12716","newborn respiratory distress syndrome","omim","267450"
< "0090021","split hand-foot malformation 1","omim","183600"
---
> "543","dystonia","omim","128100"
> "0110619","primary ciliary dyskinesia 33","omim","616726"
> "0080352","X-linked chondrodysplasia punctata 2","omim","302960"
> "0080103","cylindrical spirals myopathy","omim","160990"
12568a26475
> "14175","von Hippel-Lindau disease","omim","193300"
12571,12572c26478,26480
< "891","progressive myoclonus epilepsy","omim","612437"
< "3310","atopic dermatitis","omim","603165"
---
> "0111448","progressive myoclonus epilepsy 1B","omim","612437"
> "0111522","autosomal recessive progressive external ophthalmoplegia 1","omim","258450"
> "0050811","congenital adrenal hyperplasia","omim","201710"
12573a26482
> "12557","Duane retraction syndrome","omim","126800"
12578a26488
> "0111353","arthrogryposis, renal dysfunction, and cholestasis 1","omim","208085"
12582a26493,26494
> "0080057","autosomal recessive spinocerebellar ataxia 15","omim","615705"
> "0110343","osteogenesis imperfecta type 14","omim","615066"
12584,12585c26496,26498
< "12858","Huntington's disease","omim","143100"
< "0110966","brachydactyly type A3","omim","112700"
---
> "0110324","hypertrophic cardiomyopathy 18","omim","613874"
> "0110651","long QT syndrome 10","omim","611819"
> "0080565","congenital disorder of glycosylation Im","omim","610768"
12587,12589c26500,26509
< "0060642","recessive dystrophic epidermolysis bullosa","omim","226600"
< "1338","congenital dyserythropoietic anemia","omim","224120"
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","614499"
---
> "0080559","congenital disorder of glycosylation Ig","omim","607143"
> "0070205","familial partial lipodystrophy type 4","omim","613877"
> "0111321","idiopathic generalized epilepsy 7","omim","604827"
> "12558","chronic progressive external ophthalmoplegia","omim","157640"
> "0111420","familial GPIHBP1 deficiency","omim","615947"
> "0111398","congenital dyserythropoietic anemia type Ia","omim","224120"
> "0080545","hyper IgE syndrome","omim","147060"
> "0080512","Meier-Gorlin syndrome 1","omim","224690"
> "2951","motion sickness","omim","158280"
> "2352","hemochromatosis","omim","231100"
12590a26511
> "0111251","Parkinson's disease 21","omim","616361"
12597c26518,26519
< "0110078","Leber congenital amaurosis 1","omim","204000"
---
> "0111440","optic atrophy 4","omim","605293"
> "0060268","pontocerebellar hypoplasia type 2B","omim","612389"
12602,12606c26524,26528
< "0050588","muscular dystrophy-dystroglycanopathy","omim","613154"
< "0060799","syndromic X-linked intellectual disability Lubs type","omim","300260"
< "0110905","inflammatory bowel disease 22","omim","612380"
< "0110884","inflammatory bowel disease 23","omim","612381"
< "0050588","muscular dystrophy-dystroglycanopathy","omim","613150"
---
> "0050764","Armfield syndrome","omim","300261"
> "0050588","muscular dystrophy-dystroglycanopathy","omim","613155"
> "0050588","muscular dystrophy-dystroglycanopathy","omim","613152"
> "0110769","hereditary spastic paraplegia 16","omim","300266"
> "0111240","congenital muscular dystrophy-dystroglycanopathy type A2","omim","613150"
12608c26530
< "11830","myopia","omim","310460"
---
> "1067","open-angle glaucoma","omim","611276"
12609a26532,26533
> "560","jaw-winking syndrome","omim","154600"
> "0080150","adrenocorticotropic hormone deficiency","omim","201400"
12610a26535
> "14780","KBG syndrome","omim","148050"
12614a26540
> "0080101","Compton-North congenital myopathy","omim","612540"
12617c26543,26545
< "0070263","congenital disorder of glycosylation type IIk","omim","614727"
---
> "0080244","Galloway-Mowat syndrome 2","omim","301006"
> "0111508","Torrance type platyspondylic dysplasia","omim","151210"
> "0060737","junctional epidermolysis bullosa Herlitz type","omim","226700"
12619c26547
< "0110538","autosomal recessive nonsyndromic deafness 96","omim","614414"
---
> "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","omim","615630"
12622c26550
< "0110823","hereditary spastic paraplegia 8","omim","603563"
---
> "0080250","erythrokeratodermia variabilis et progressiva 4","omim","617526"
12624c26552
< "0110097","short-rib thoracic dysplasia 9 with or without polydactyly","omim","266920"
---
> "0110990","Joubert syndrome 21","omim","615636"
12628c26556
< "0070177","spermatogenic failure 22","omim","617706"
---
> "0060565","Ritscher-Schinzel syndrome","omim","220210"
12630c26558,26559
< "0060885","renal hypomagnesemia 2","omim","154020"
---
> "0080308","myofibrillar myopathy 8","omim","617258"
> "0080482","peroxisome biogenesis disorder 7A","omim","614872"
12634,12635c26563,26564
< "0110620","primary ciliary dyskinesia 35","omim","617092"
< "0110610","primary ciliary dyskinesia 34","omim","617091"
---
> "0110127","Bardet-Biedl syndrome 5","omim","615983"
> "0080314","cone-rod dystrophy 14","omim","602093"
12636a26566
> "2058","chronic mucocutaneous candidiasis","omim","607644"
12637a26568
> "0110037","Alzheimer's disease 5","omim","602096"
12639c26570
< "14737","craniofrontonasal syndrome","omim","304110"
---
> "9955","hypoplastic left heart syndrome","omim","241550"
12641c26572,26573
< "0110029","alpha thalassemia-intellectual disability syndrome type 1","omim","141750"
---
> "0111184","myopathy, lactic acidosis, and sideroblastic anemia 3","omim","500011"
> "0080253","Meckel syndrome 13","omim","617562"
12644c26576
< "0110317","hypertrophic cardiomyopathy 11","omim","612098"
---
> "0050657","Bannayan-Riley-Ruvalcaba syndrome","omim","158350"
12647c26579,26580
< "0050629","Aicardi-Goutieres syndrome","omim","615010"
---
> "0111326","juvenile myoclonic epilepsy 3","omim","608816"
> "0060307","autosomal dominant non-syndromic intellectual disability","omim","156200"
12649c26582,26583
< "0110376","retinitis pigmentosa 41","omim","612095"
---
> "0060449","gelatinous drop-like corneal dystrophy","omim","204870"
> "0080502","GM1 gangliosidosis type 1","omim","230500"
12650a26585
> "0111058","platelet-type bleeding disorder 12","omim","605735"
12652a26588
> "0080506","Cornelia de Lange syndrome 2","omim","300590"
12654,12655c26590,26591
< "00600891","juvenile onset Parkinson's disease 19A","omim","615528"
< "0050885","IMAGe syndrome","omim","614732"
---
> "0060891","Parkinson's disease 19A","omim","615528"
> "0090039","torsion dystonia 6","omim","602629"
12657,12658c26593,26599
< "0060882","renal hypomagnesemia 4","omim","611718"
< "5212","congenital disorder of glycosylation","omim","212065"
---
> "0060558","lethal congenital contracture syndrome","omim","253310"
> "0060550","ablepharon macrostomia syndrome","omim","200110"
> "9821","choroideremia","omim","303100"
> "0060424","chromosome 6q24-q25 deletion syndrome","omim","612863"
> "0111158","SADDAN","omim","616482"
> "0050570","congenital disorder of glycosylation type I","omim","212065"
> "0050571","congenital disorder of glycosylation type II","omim","212066"
12659a26601
> "0111428","essential tremor 1","omim","190300"
12660a26603,26604
> "0111260","phosphoribosylpyrophosphate synthetase superactivity","omim","300661"
> "0080436","early infantile epileptic encephalopathy 4","omim","612164"
12661a26606
> "13941","benign paroxysmal positional nystagmus","omim","193007"
12665c26610,26611
< "0060228","intracranial berry aneurysm","omim","612162"
---
> "0080464","early infantile epileptic encephalopathy 53","omim","617389"
> "0050979","spinocerebellar ataxia type 30","omim","613371"
12666a26613,26614
> "12961","Poland syndrome","omim","173800"
> "0110224","Brugada syndrome 7","omim","613120"
12667a26616,26617
> "0111278","histiocytosis-lymphadenopathy plus syndrome","omim","602782"
> "0111244","palmoplantar keratoderma and congenital alopecia 1","omim","104100"
12669c26619,26620
< "0070090","schizophrenia 14","omim","612361"
---
> "0110522","autosomal recessive nonsyndromic deafness 71","omim","612789"
> "0060452","posterior amorphous corneal dystrophy","omim","612868"
12671a26623
> "0110462","autosomal recessive nonsyndromic deafness 101","omim","615837"
12674c26626,26627
< "4990","essential tremor","omim","190300"
---
> "0080112","mitochondrial complex III deficiency nuclear type 3","omim","615158"
> "0060847","Leri-Weill dyschondrosteosis","omim","127300"
12675a26629
> "0110638","congenital muscular dystrophy merosin-positive","omim","609456"
12678a26633
> "0111246","amyotrophic lateral sclerosis-parkinsonism/dementia complex 1","omim","105500"
12680c26635
< "13774","Addison's disease","omim","240200"
---
> "0050567","orofacial cleft","omim","119530"
12681a26637
> "13922","eosinophilic esophagitis","omim","613412"
12683a26640
> "0060008","janus kinase-3 deficiency","omim","600802"
12684a26642,26644
> "0110611","primary ciliary dyskinesia 27","omim","615504"
> "0090044","dystonia 9","omim","601042"
> "0111546","Currarino syndrome","omim","176450"
12686,12687c26646,26648
< "0050712","AGAT deficiency","omim","612718"
< "11830","myopia","omim","612717"
---
> "0050689","brachydactyly-syndactyly syndrome","omim","610713"
> "0050540","Charcot-Marie-Tooth disease type 3","omim","145900"
> "0060421","chromosome 5q12 deletion syndrome","omim","615668"
12690c26651,26653
< "0060199","amyotrophic lateral sclerosis type 7","omim","608031"
---
> "0110627","primary ciliary dyskinesia 26","omim","615500"
> "0110482","autosomal recessive nonsyndromic deafness 24","omim","611022"
> "0080443","early infantile epileptic encephalopathy 21","omim","615833"
12693c26656
< "0110462","autosomal recessive nonsyndromic deafness 101","omim","615837"
---
> "8923","skin melanoma","omim","608035"
12695c26658,26661
< "0111030","hemochromatosis type 3","omim","604250"
---
> "4428","dyslexia","omim","604254"
> "0080117","mitochondrial complex III deficiency nuclear type 8","omim","615838"
> "9240","erythromelalgia","omim","133020"
> "0111583","carboxypeptidase N deficiency","omim","212070"
12697c26663
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","615802"
---
> "0060025","immunoglobulin alpha deficiency","omim","609529"
12699,12700c26665,26667
< "0060838","isolated microphthalmia 7","omim","613704"
< "10426","Klippel-Feil syndrome","omim","613702"
---
> "8986","narcolepsy","omim","609039"
> "0080592","Klippel-Feil syndrome 3","omim","613702"
> "0080592","Klippel-Feil syndrome 4","omim","613702"
12705c26672,26675
< "891","progressive myoclonus epilepsy","omim","614018"
---
> "0080072","neuronal intestinal dysplasia","omim","601223"
> "3012","Li-Fraumeni syndrome","omim","151623"
> "0111449","progressive myoclonus epilepsy 6","omim","614018"
> "0050453","lissencephaly","omim","614019"
12706a26677,26680
> "13641","exfoliation syndrome","omim","177650"
> "6225","Cronkhite-Canada syndrome","omim","175500"
> "14693","Clouston syndrome","omim","129500"
> "384","Wolff-Parkinson-White syndrome","omim","194200"
12710c26684
< "0111064","autosomal recessive distal spinal muscular atrophy 1","omim","604320"
---
> "0111064","distal spinal muscular atrophy 1","omim","604320"
12712c26686
< "11830","myopia","omim","609995"
---
> "0050963","spinocerebellar ataxia type 13","omim","605259"
12713a26688
> "0050962","spinocerebellar ataxia type 12","omim","604326"
12716a26692,26693
> "0090078","hypogonadotropic hypogonadism 7 with or without anosmia","omim","146110"
> "0080214","punctate palmoplantar keratoderma type 1A","omim","148600"
12721c26698,26699
< "0110158","Charcot-Marie-Tooth disease type 2I","omim","607677"
---
> "14004","thoracic aortic aneurysm","omim","132900"
> "0080139","multiple congenital anomalies-hypotonia-seizures syndrome 2","omim","300868"
12724c26702,26703
< "0070176","spermatogenic failure 4","omim","270960"
---
> "0090037","torsion dystonia 13","omim","607671"
> "9273","citrullinemia","omim","605814"
12737c26716,26717
< "0050779","hydrolethalus syndrome","omim","614120"
---
> "0110763","hereditary spastic paraplegia 10","omim","604187"
> "0110021","age related macular degeneration 9","omim","611378"
12740a26721
> "11383","cryptorchidism","omim","219050"
12741a26723
> "0050857","Perrault syndrome","omim","614129"
12743c26725,26726
< "0110962","brachydactyly-preaxial hallux varus syndrome","omim","112450"
---
> "0110535","autosomal recessive nonsyndromic deafness 9","omim","601071"
> "14452","hypokalemic periodic paralysis","omim","170400"
12749a26733
> "0111261","fumarase deficiency","omim","606812"
12751c26735,26737
< "10426","Klippel-Feil syndrome","omim","214300"
---
> "0080251","erythrokeratodermia variabilis et progressiva 5","omim","617756"
> "0111274","CODAS syndrome","omim","600373"
> "12177","common variable immunodeficiency","omim","613496"
12754a26741,26742
> "0060599","Nance-Horan syndrome","omim","302350"
> "0070266","congenital disorder of glycosylation type IIn","omim","616721"
12757,12758c26745,26748
< "0110619","primary ciliary dyskinesia 33","omim","616726"
< "1064","cystinosis","omim","219800"
---
> "0060239","Van der Woude syndrome","omim","119300"
> "0080451","early infantile epileptic encephalopathy 29","omim","616339"
> "0090047","paroxysmal nonkinesigenic dyskinesia 2","omim","611147"
> "0080274","multiple mitochondrial dysfunctions syndrome 5","omim","617613"
12760c26750,26751
< "0050776","non-syndromic X-linked intellectual disability","omim","300912"
---
> "0110984","Joubert syndrome 15","omim","614464"
> "0060785","adult-onset autosomal dominant demyelinating leukodystrophy","omim","169500"
12762c26753,26756
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","614342"
---
> "0090021","split hand-foot malformation 1","omim","183600"
> "0111263","combined malonic and methylmalonic acidemia","omim","614265"
> "0111322","idiopathic generalized epilepsy 8","omim","612899"
> "9206","Barrett's esophagus","omim","614266"
12763a26758,26759
> "0110225","Brugada syndrome 8","omim","613123"
> "0080033","craniometaphyseal dysplasia","omim","122860"
12766c26762,26766
< "0090027","split hand-foot malformation 2","omim","313350"
---
> "0111513","metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome","omim","156510"
> "0110886","inflammatory bowel disease 9","omim","608448"
> "2732","Rothmund-Thomson syndrome","omim","268400"
> "1339","Diamond-Blackfan anemia","omim","610629"
> "0070194","autosomal recessive chronic granulomatous disease cytochrome b-positive type III","omim","613960"
12768,12769c26768,26769
< "13241","Behcet's disease","omim","109650"
< "0090115","spinocerebellar ataxia type 1 with axonal neuropathy","omim","607250"
---
> "0060774","congenital diarrhea","omim","214700"
> "4428","dyslexia","omim","600202"
12770a26771,26772
> "12177","common variable immunodeficiency","omim","613494"
> "14219","renal tubular acidosis","omim","267200"
12774a26777
> "8446","intussusception","omim","147710"
12775a26779
> "12306","vitiligo","omim","193200"
12776a26781
> "0090054","episodic kinesigenic dyskinesia 2","omim","611031"
12779a26785,26786
> "0111578","Gillespie syndrome","omim","206700"
> "13357","chondromalacia patellae","omim","168900"
12781c26788
< "0060842","isolated microphthalmia 3","omim","611038"
---
> "0060405","chromosome 17q23.1-q23.2 deletion syndrome","omim","613355"
12784a26792
> "397","restrictive cardiomyopathy","omim","115210"
12788a26797
> "0080215","early infantile epileptic encephalopathy 8","omim","300607"
12789a26799,26803
> "0111333","early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome","omim","614399"
> "11633","thyroid hormone resistance syndrome","omim","188570"
> "0070278","primary autosomal recessive microcephaly 7","omim","612703"
> "0111200","distal hereditary motor neuronopathy type 1","omim","182960"
> "0080551","Naxos disease","omim","601214"
12792,12793c26806
< "0060341","agnathia-otocephaly complex","omim","202650"
< "14762","calcaneonavicular coalition","omim","186400"
---
> "14711","FG syndrome","omim","305450"
12794a26808
> "0080385","nephrotic syndrome type 11","omim","616730"
12796,12797c26810,26817
< "0070232","benign recurrent intrahepatic cholestasis 2","omim","605479"
< "0050811","congenital adrenal hyperplasia","omim","201710"
---
> "0111434","optic atrophy 10","omim","616732"
> "0080538","Sweeney-Cox syndrome","omim","617746"
> "0111383","autosomal dominant keratitis","omim","148190"
> "0111454","SHORT syndrome","omim","269880"
> "0070285","primary autosomal recessive microcephaly 1","omim","251200"
> "0111339","Vohwinkel syndrome","omim","124500"
> "3310","atopic dermatitis","omim","603165"
> "12783","migraine without aura","omim","607501"
12800a26821,26822
> "0060776","congenital diarrhea 5 with tufting enteropathy","omim","613217"
> "0060247","Smith-McCort dysplasia","omim","607326"
12802c26824,26825
< "10825","essential hypertension","omim","607329"
---
> "0080316","megalencephalic leukoencephalopathy with subcortical cysts 1","omim","604004"
> "0111338","isolated elevated serum creatine phosphokinase levels","omim","123320"
12805,12806c26828,26830
< "14798","Blount's disease","omim","188700"
< "0050588","muscular dystrophy-dystroglycanopathy","omim","614643"
---
> "9256","colorectal cancer","omim","114500"
> "12858","Huntington's disease","omim","143100"
> "0080028","spondyloepimetaphyseal dysplasia, Strudwick type","omim","184250"
12807a26832,26835
> "0111499","combined oxidative phosphorylation deficiency 37","omim","618329"
> "0060240","UV-sensitive syndrome","omim","614640"
> "0080046","Stickler syndrome","omim","108300"
> "0110351","osteogenesis imperfecta type 11","omim","610968"
12809,12810c26837,26841
< "0110744","type 1 diabetes mellitus 5","omim","600320"
< "0080053","Albright's hereditary osteodystrophy","omim","103580"
---
> "0111443","optic atrophy 2","omim","311050"
> "0050428","nonepidermolytic palmoplantar keratoderma","omim","615735"
> "0111421","familial apolipoprotein A5 deficiency","omim","144650"
> "0050944","spastic ataxia 5","omim","614487"
> "0110053","amelogenesis imperfecta type 4","omim","104510"
12812c26843,26846
< "0060785","adult-onset autosomal dominant demyelinating leukodystrophy","omim","169500"
---
> "0060263","porencephaly","omim","614483"
> "3389","Papillon-Lefevre disease","omim","245000"
> "0080223","epidermolytic palmoplantar keratoderma","omim","144200"
> "0060911","karyomegalic interstitial nephritis","omim","614817"
12814c26848
< "0090145","dopamine beta-hydroxylase deficiency","omim","223360"
---
> "0090092","hypogonadotropic hypogonadism 3 with or without anosmia","omim","244200"
12816,12819c26850,26857
< "0110976","brachydactyly type E2","omim","613382"
< "14448","46 XY gonadal dysgenesis","omim","614279"
< "0080208","nonalcoholic fatty liver disease","omim","613387"
< "0050560","Walker-Warburg syndrome","omim","253280"
---
> "0060761","familial chronic myelocytic leukemia-like syndrome","omim","600080"
> "14557","primary pulmonary hypertension","omim","615343"
> "0110987","Joubert syndrome 18","omim","614815"
> "0080208","non-alcoholic fatty liver disease","omim","613387"
> "0050727","tyrosinemia type III","omim","276710"
> "0060481","Goldberg-Shprintzen syndrome","omim","609460"
> "14766","renal agenesis","omim","191830"
> "0111548","ring dermoid of cornea","omim","180550"
12821c26859,26860
< "0110226","Brugada syndrome 9","omim","616399"
---
> "0110077","arrhythmogenic right ventricular dysplasia 9","omim","609040"
> "0090036","myoclonic dystonia 26","omim","616398"
12823,12824c26862,26864
< "0110865","congenital stationary night blindness 1B","omim","257270"
< "1339","Diamond-Blackfan anemia","omim","606129"
---
> "14791","Leber congenital amaurosis","omim","204000"
> "0060269","pontocerebellar hypoplasia type 2C","omim","612390"
> "0070068","autosomal dominant non-syndromic intellectual disability 38","omim","616393"
12826,12827c26866,26868
< "0060578","Noonan syndrome 1","omim","163950"
< "1062","Fanconi syndrome","omim","615605"
---
> "0060385","acrofacial dysostosis, Patagonia type","omim","601829"
> "0060284","paroxysmal nocturnal hemoglobinuria","omim","300818"
> "12388","neurohypophyseal diabetes insipidus","omim","125700"
12830c26871,26872
< "11830","myopia","omim","612554"
---
> "0110703","hypotrichosis 6","omim","607903"
> "0070218","familial hyperinsulinemic hypoglycemia 2","omim","601820"
12833a26876,26879
> "0070159","hereditary sensory neuropathy X-linked","omim","310470"
> "12707","myoclonic cerebellar dyssynergia","omim","213400"
> "0080111","mitochondrial complex III deficiency nuclear type 1","omim","124000"
> "0090048","dystonia 16","omim","612067"
12834a26881
> "0111533","gnathodiaphyseal dysplasia","omim","166260"
12838c26885,26886
< "2247","spondylosis","omim","184300"
---
> "0050885","IMAGe syndrome","omim","614732"
> "0080351","CLOVES syndrome","omim","612918"
12840c26888
< "0050529","adult spinal muscular atrophy","omim","271150"
---
> "0110781","hereditary spastic paraplegia 30","omim","610357"
12844c26892
< "0110070","arrhythmogenic right ventricular dysplasia 1","omim","107970"
---
> "0080119","mitochondrial DNA depletion syndrome 1","omim","603041"
12846d26893
< "0110363","retinitis pigmentosa 71","omim","616394"
12850a26898,26905
> "13096","Sneddon syndrome","omim","182410"
> "0111286","psoriasis 1","omim","177900"
> "0111523","autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3","omim","617069"
> "0080198","infantile histiocytoid cardiomyopathy","omim","500000"
> "4751","striatonigral degeneration","omim","500003"
> "0080427","early infantile epileptic encephalopathy 40","omim","617065"
> "0080460","early infantile epileptic encephalopathy 34","omim","616645"
> "0080518","Meier-Gorlin syndrome 7","omim","617063"
12853a26909,26910
> "5485","synovial sarcoma","omim","300813"
> "0080218","primary spontaneous pneumothorax","omim","173600"
12855c26912,26915
< "4795","GM2 gangliosidosis, AB variant","omim","272750"
---
> "0090058","torsion dystonia with onset in infancy","omim","602554"
> "0110445","dilated cardiomyopathy 1KK","omim","615248"
> "0111253","neurofibromatosis 1","omim","162210"
> "0111235","congenital muscular dystrophy-dystroglycanopathy type A12","omim","615249"
12861c26921
< "0050662","bestrophinopathy","omim","611809"
---
> "0111571","Weyers acrofacial dysostosis","omim","193530"
12866a26927,26928
> "0080430","early infantile epileptic encephalopathy 65","omim","618008"
> "0060738","junctional epidermolysis bullosa non-Herlitz type","omim","226650"
12867a26930
> "12177","common variable immunodeficiency","omim","613493"
12870a26934
> "0111186","myopathy, lactic acidosis, and sideroblastic anemia 2","omim","613561"
12871a26936
> "0050978","spinocerebellar ataxia type 29","omim","117360"
12874,12876c26939,26949
< "0060372","autosomal recessive early-onset Parkinson's disease 15","omim","260300"
< "0110793","hereditary spastic paraplegia 41","omim","613364"
< "0110909","inflammatory bowel disease 25","omim","612567"
---
> "0060414","chromosome 2p12-p11.2 deletion syndrome","omim","613564"
> "0080544","hyper IgM syndrome","omim","308230"
> "0080236","autosomal dominant mental retardation 45","omim","617600"
> "0080237","autosomal dominant mental retardation 46","omim","617601"
> "0080268","autosomal dominant nonsyndromic deafness 72","omim","617606"
> "0060372","Parkinson's disease 15","omim","260300"
> "4253","melorheostosis","omim","155950"
> "0060582","Noonan syndrome 4","omim","610733"
> "0111483","combined oxidative phosphorylation deficiency 2","omim","610498"
> "0111296","generalized epilepsy with febrile seizures plus 10","omim","618482"
> "0080318","megalencephalic leukoencephalopathy with subcortical cysts 2A","omim","613925"
12877a26951
> "10604","lactose intolerance","omim","223100"
12879c26953
< "1067","open-angle glaucoma","omim","602429"
---
> "0080480","peroxisome biogenesis disorder 5A","omim","614866"
12881c26955
< "4362","cervical cancer","omim","603956"
---
> "0080479","peroxisome biogenesis disorder 4A","omim","614862"
12882a26957
> "0090051","dystonia 23","omim","614860"
12884c26959,26961
< "0060246","MASA syndrome","omim","303350"
---
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","614499"
> "0080568","congenital disorder of glycosylation Iq","omim","612379"
> "9074","systemic lupus erythematosus","omim","612378"
12885a26963
> "0060228","intracranial berry aneurysm","omim","610213"
12888c26966,26968
< "1485","cystic fibrosis","omim","219700"
---
> "0060354","Stormorken syndrome","omim","185070"
> "0050691","branchiooculofacial syndrome","omim","113620"
> "0110727","neuronal ceroid lipofuscinosis 13","omim","615362"
12889a26970,26971
> "0080098","myofibrillar myopathy 7","omim","617114"
> "0080447","early infantile epileptic encephalopathy 43","omim","617113"
12891c26973,26974
< "14330","Parkinson's disease","omim","168600"
---
> "0060791","hypomyelinating leukodystrophy 9","omim","616140"
> "0111303","familial febrile seizures 9","omim","611634"
12893c26976
< "0110736","neurodegeneration with brain iron accumulation 2b","omim","610217"
---
> "0050577","Sensenbrenner syndrome","omim","218330"
12899a26983,26986
> "0080441","early infantile epileptic encephalopathy 49","omim","617281"
> "0111509","lymphedema-distichiasis syndrome","omim","153400"
> "0111308","familial febrile seizures 11","omim","614418"
> "0110595","Stromme syndrome","omim","243605"
12902a26990
> "14692","Smith-Lemli-Opitz syndrome","omim","270400"
12903a26992,26993
> "0060060","non-Hodgkin lymphoma","omim","605027"
> "0110710","hypotrichosis 13","omim","615896"
12905c26995,26996
< "0110248","cataract 30","omim","116300"
---
> "1099","alpha thalassemia","omim","604131"
> "8158","complement component 5 deficiency","omim","609536"
12907c26998,26999
< "0060193","amyotrophic lateral sclerosis type 1","omim","105400"
---
> "11830","myopia","omim","612554"
> "4252","Alexander disease","omim","203450"
12908a27001,27002
> "10383","amyotrophic neuralgia","omim","162100"
> "1067","open-angle glaucoma","omim","608696"
12913c27007,27008
< "0050710","3-Methylcrotonyl-CoA carboxylase deficiency","omim","210200"
---
> "0080579","3-Methylcrotonyl-CoA carboxylase 1 deficiency","omim","210200"
> "0060402","chromosome 17p13.1 deletion syndrome","omim","613776"
12915a27011
> "891","progressive myoclonus epilepsy","omim","254800"
12916a27013,27014
> "8354","complement component 3 deficiency","omim","613779"
> "12387","nephrogenic diabetes insipidus","omim","304800"
12919c27017,27020
< "0050646","distal arthrogryposis","omim","193700"
---
> "0090132","complex cortical dysplasia with other brain malformations 7","omim","610031"
> "0080336","mitochondrial DNA depletion syndrome 14","omim","616896"
> "0080387","nephrotic syndrome type 12","omim","616892"
> "0080381","nephrotic syndrome type 13","omim","616893"
12920a27022
> "0060275","pontocerebellar hypoplasia type 6","omim","611523"
12923,12924c27025,27029
< "0060245","Mast syndrome","omim","248900"
< "0050560","Walker-Warburg syndrome","omim","236670"
---
> "0111107","maturity-onset diabetes of the young type 9","omim","612225"
> "0110157","Charcot-Marie-Tooth disease type 2J","omim","607736"
> "0050557","congenital muscular dystrophy","omim","254100"
> "0080563","congenital disorder of glycosylation Ik","omim","608540"
> "0111237","congenital muscular dystrophy-dystroglycanopathy type A1","omim","236670"
12929c27034,27036
< "0060900","autosomal recessive Parkinson's disease 14","omim","612953"
---
> "0080072","neuronal intestinal dysplasia","omim","243180"
> "0111291","psoriasis 12","omim","612950"
> "0060169","benign familial infantile epilepsy","omim","601764"
12932c27039,27040
< "1858","McCune Albright syndrome","omim","174800"
---
> "0080097","myofibrillar myopathy 6","omim","612954"
> "12918","thromboangiitis obliterans","omim","211480"
12934c27042
< "0110705","hypotrichosis 8","omim","278150"
---
> "0050781","Ogden syndrome","omim","300855"
12942,12943c27050,27051
< "0060812","syndromic X-linked intellectual disability Siderius type","omim","300263"
< "0110756","type 1 diabetes mellitus 19","omim","610155"
---
> "0060751","familial temporal lobe epilepsy 7","omim","616436"
> "0110624","primary ciliary dyskinesia 30","omim","616037"
12945c27053
< "0110506","autosomal recessive nonsyndromic deafness 49","omim","610153"
---
> "0060451","Meesmann corneal dystrophy","omim","122100"
12948c27056
< "0060233","cardiofaciocutaneous syndrome","omim","615280"
---
> "0111463","cardiofaciocutaneous syndrome 4","omim","615280"
12951,12952c27059,27060
< "0110194","Charcot-Marie-Tooth disease type 4B3","omim","615284"
< "0050764","Armfield syndrome","omim","300261"
---
> "0110098","atopic dermatitis 2","omim","605803"
> "12580","Cri-Du-Chat syndrome","omim","123450"
12954c27062
< "0050588","muscular dystrophy-dystroglycanopathy","omim","615287"
---
> "0110744","type 1 diabetes mellitus 5","omim","600320"
12957c27065
< "13945","CADASIL","omim","600142"
---
> "0111081","Fanconi anemia complementation group T","omim","616435"
12960c27068,27069
< "0050588","muscular dystrophy-dystroglycanopathy","omim","613152"
---
> "0110905","inflammatory bowel disease 22","omim","612380"
> "0060400","chromosome 16p12.2-p11.2 deletion syndrome","omim","613604"
12962,12963c27071
< "0060378","orofaciodigital syndrome VIII","omim","300484"
< "0050588","muscular dystrophy-dystroglycanopathy","omim","613153"
---
> "0110884","inflammatory bowel disease 23","omim","612381"
12965c27073,27074
< "0110388","retinitis pigmentosa 10","omim","180105"
---
> "0110593","autosomal dominant nonsyndromic deafness 9","omim","601369"
> "0080557","congenital disorder of glycosylation Ie","omim","608799"
12967c27076
< "13099","Moyamoya disease","omim","608796"
---
> "0050809","mucopolysaccharidosis IX","omim","601492"
12970,12971c27079,27085
< "3526","cerebral infarction","omim","601367"
< "0050650","familial atrial fibrillation","omim","607554"
---
> "2583","agammaglobulinemia","omim","601495"
> "0111382","ischiocoxopodopatellar syndrome","omim","147891"
> "4624","Ollier disease","omim","166000"
> "0110565","autosomal dominant nonsyndromic deafness 3B","omim","612643"
> "11830","myopia","omim","310460"
> "2512","nevoid basal cell carcinoma syndrome","omim","109400"
> "1929","supravalvular aortic stenosis","omim","185500"
12974,12975c27088,27090
< "0060743","methylmalonic acidemia cblB type","omim","251110"
< "0050848","obstructive sleep apnea","omim","107650"
---
> "0111242","congenital muscular dystrophy-dystroglycanopathy type A6","omim","613154"
> "0080564","congenital disorder of glycosylation Il","omim","608776"
> "14448","46 XY gonadal dysgenesis","omim","300018"
12977a27093
> "0110976","brachydactyly type E2","omim","613382"
12979a27096
> "0090060","Wolcott-Rallison syndrome","omim","226980"
12982c27099,27100
< "0050588","muscular dystrophy-dystroglycanopathy","omim","615350"
---
> "1919","Lesch-Nyhan syndrome","omim","300322"
> "0111233","congenital muscular dystrophy-dystroglycanopathy A14","omim","615350"
12985c27103
< "0050690","brachyolmia","omim","113500"
---
> "0110416","retinitis pigmentosa 24","omim","300155"
12986a27105
> "0111540","prolidase deficiency","omim","170100"
12989c27108
< "0070040","autosomal dominant non-syndromic intellectual disability 10","omim","614256"
---
> "0050454","periventricular nodular heterotopia","omim","612881"
12990a27110
> "9884","muscular dystrophy","omim","158800"
12991a27112
> "11719","oculopharyngeal muscular dystrophy","omim","164300"
12992a27114
> "0110736","neurodegeneration with brain iron accumulation 2b","omim","610217"
12994,12996c27116,27120
< "0060371","autosomal dominant Parkinson's disease 8","omim","607060"
< "0110534","autosomal recessive nonsyndromic deafness 89","omim","613916"
< "14448","46 XY gonadal dysgenesis","omim","233420"
---
> "0060371","Parkinson's disease 8","omim","607060"
> "0050833","orotic aciduria","omim","258900"
> "0111314","idiopathic generalized epilepsy 13","omim","611136"
> "0050654","Baller-Gerold syndrome","omim","218600"
> "0060399","chromosome 16p12.1 deletion syndrome, 520kb","omim","136570"
12997a27122,27124
> "0080090","reducing body myopathy","omim","300718"
> "0111375","fetal akinesia deformation sequence syndrome","omim","208150"
> "0111586","Martsolf syndrome","omim","212720"
12999c27126
< "0110490","autosomal recessive nonsyndromic deafness 31","omim","607084"
---
> "0060706","X-linked lymphoproliferative syndrome 2","omim","300635"
13000a27128
> "14004","thoracic aortic aneurysm","omim","607086"
13002c27130
< "10892","hypospadias","omim","300633"
---
> "10591","pre-eclampsia","omim","614592"
13003a27132
> "0111359","large congenital melanocytic nevus","omim","137550"
13009c27138,27142
< "701","dentin dysplasia","omim","125420"
---
> "0090052","dystonia 24","omim","615034"
> "0110721","neuronal ceroid lipofuscinosis 1","omim","256730"
> "0080090","reducing body myopathy","omim","300717"
> "0060730","torsion dystonia 1","omim","128100"
> "0110704","hypotrichosis 7","omim","604379"
13014,13015c27147,27148
< "0060710","autosomal recessive congenital ichthyosis 2","omim","242100"
< "0070012","Seckel syndrome 5","omim","613823"
---
> "0060303","complement component 9 deficiency","omim","613825"
> "5325","Roberts syndrome","omim","268300"
13016a27150
> "9869","hereditary fructose intolerance syndrome","omim","229600"
13017a27152,27154
> "12704","ataxia telangiectasia","omim","208900"
> "0070055","Xia-Gibbs Syndrome","omim","615829"
> "0080226","autosomal dominant mental retardation 56","omim","617854"
13019c27156
< "0060170","generalized epilepsy with febrile seizures plus","omim","613828"
---
> "0111299","generalized epilepsy with febrile seizures plus 8","omim","613828"
13020a27158
> "0111328","juvenile myoclonic epilepsy 9","omim","614280"
13021a27160,27161
> "11555","Fuchs' endothelial dystrophy","omim","613270"
> "0080575","Larsen-like syndrome B3GAT3 type","omim","245600"
13024c27164,27166
< "0110589","autosomal dominant nonsyndromic deafness 68","omim","616707"
---
> "0070263","congenital disorder of glycosylation type IIk","omim","614727"
> "2583","agammaglobulinemia","omim","601495"
> "0080584","autosomal dominant Wolfram syndrome","omim","614296"
13027c27169
< "10908","hydrocephalus","omim","307000"
---
> "0110374","retinitis pigmentosa 68","omim","615725"
13031d27172
< "0110091","short-rib thoracic dysplasia 10 with or without polydactyly","omim","615630"
13034a27176
> "0111289","psoriasis 10","omim","612410"
13037,13038c27179,27180
< "0060811","syndromic X-linked intellectual disability Turner type","omim","300706"
< "1338","congenital dyserythropoietic anemia","omim","224100"
---
> "0110586","autosomal dominant nonsyndromic deafness 65","omim","616044"
> "0111311","familial febrile seizures 7","omim","611515"
13042,13043c27184,27185
< "0060581","Noonan syndrome 3","omim","609942"
< "3652","Leigh disease","omim","220111"
---
> "3762","cytochrome-c oxidase deficiency disease","omim","220110"
> "0111180","French Canadian Leigh disease","omim","220111"
13046,13047c27188,27197
< "0060828","X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome","omim","300886"
< "0110990","Joubert syndrome 21","omim","615636"
---
> "0111350","Laurin-Sandrow syndrome","omim","135750"
> "14448","46 XY gonadal dysgenesis","omim","613762"
> "1415","gyrate atrophy","omim","258870"
> "0080249","erythrokeratodermia variabilis et progressiva 3","omim","617525"
> "0050794","multiple synostoses syndrome","omim","186500"
> "1067","open-angle glaucoma","omim","611274"
> "0111404","Jalili syndrome","omim","217080"
> "0111288","psoriasis 8","omim","610707"
> "0110414","retinitis pigmentosa 3","omim","300029"
> "0080248","erythrokeratodermia variabilis et progressiva 2","omim","617524"
13050c27200
< "1067","open-angle glaucoma","omim","611276"
---
> "0060331","mitochondrial complex V (ATP synthase) deficiency nuclear type 2","omim","614052"
13052,13053c27202
< "10283","prostate cancer","omim","610997"
< "4252","Alexander disease","omim","203450"
---
> "0090015","Cenani-Lenz syndactyly syndrome","omim","212780"
13054a27204
> "0070272","hereditary nonpolyposis colorectal cancer type 5","omim","614350"
13057c27207,27209
< "0050535","exudative vitreoretinopathy","omim","601813"
---
> "0110731","neuronal ceroid lipofuscinosis 3","omim","204200"
> "0111411","exudative vitreoretinopathy 4","omim","601813"
> "0090050","dystonia 27","omim","616411"
13058a27211,27212
> "0060460","chromosome 5p13 duplication syndrome","omim","613174"
> "0080411","familial adenomatous polyposis 3","omim","616415"
13059a27214
> "12798","mucopolysaccharidosis","omim","252700"
13060a27216,27217
> "0080039","axial osteomalacia","omim","109130"
> "0080224","autosomal dominant dystrophic epidermolysis bullosa","omim","131750"
13063,13064c27220,27221
< "1339","Diamond-Blackfan anemia","omim","612563"
< "0110908","inflammatory bowel disease 24","omim","612566"
---
> "0060383","acrofacial dysostosis Rodriguez type","omim","201170"
> "9884","muscular dystrophy","omim","309950"
13065a27223
> "0111429","essential tremor 2","omim","602134"
13067a27226
> "12661","tooth ankylosis","omim","157950"
13068a27228
> "583","hemolytic anemia","omim","266120"
13070c27230,27231
< "0080482","peroxisome biogenesis disorder 7A","omim","614872"
---
> "0080363","mitochondrial pyruvate carrier deficiency","omim","614741"
> "0060885","renal hypomagnesemia 2","omim","154020"
13072,13073c27233,27234
< "3012","Li-Fraumeni syndrome","omim","609265"
< "0080208","nonalcoholic fatty liver disease","omim","613282"
---
> "0111504","Li-Fraumeni syndrome 2","omim","609265"
> "0080208","non-alcoholic fatty liver disease","omim","613282"
13074a27236
> "0080536","hypermanganesemia with dystonia 1","omim","613280"
13076a27239
> "0111489","combined oxidative phosphorylation deficiency 27","omim","616672"
13080c27243,27244
< "0111056","platelet-type bleeding disorder 3","omim","177820"
---
> "0110293","autosomal recessive limb-girdle muscular dystrophy type 2P","omim","613818"
> "0080448","early infantile epileptic encephalopathy 48","omim","617276"
13081a27246,27248
> "0111526","Mullerian aplasia and hyperandrogenism","omim","158330"
> "1339","Diamond-Blackfan anemia","omim","615550"
> "0111516","autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4","omim","617070"
13084c27251
< "0110171","Charcot-Marie-Tooth disease axonal type 2S","omim","616155"
---
> "8461","Aicardi syndrome","omim","304050"
13087c27254,27255
< "0060868","leukoencephalopathy with vanishing white matter","omim","603896"
---
> "0110948","Waardenburg syndrome type 1","omim","193500"
> "0110620","primary ciliary dyskinesia 35","omim","617092"
13089a27258
> "0050676","Birt-Hogg-Dube syndrome","omim","135150"
13090a27260
> "0110213","isolated cleft palate","omim","119540"
13092,13095c27262,27264
< "0110473","autosomal recessive nonsyndromic deafness 18A","omim","602092"
< "0080419","early infantile epileptic encephalopathy 50","omim","616457"
< "0050801","androgenic alopecia","omim","300710"
< "0050661","vitelliform macular dystrophy","omim","616151"
---
> "0060413","chromosome 22q11.2 deletion syndrome, distal","omim","611867"
> "14365","systemic primary carnitine deficiency disease","omim","212140"
> "3329","benign epilepsy with centrotemporal spikes","omim","117100"
13097c27266
< "0110611","primary ciliary dyskinesia 27","omim","615504"
---
> "0110379","retinitis pigmentosa 43","omim","613810"
13101c27270
< "0110627","primary ciliary dyskinesia 26","omim","615500"
---
> "0060638","neonatal diabetes mellitus with congenital hypothyroidism","omim","610199"
13103a27273,27276
> "0050857","Perrault syndrome","omim","614926"
> "0111493","combined oxidative phosphorylation deficiency 12","omim","614924"
> "0111279","psoriasis 7","omim","605606"
> "0111481","combined oxidative phosphorylation deficiency 11","omim","614922"
13104a27278,27279
> "0111558","Charcot-Marie-Tooth disease type 2DD","omim","618036"
> "0080570","congenital disorder of glycosylation It","omim","614921"
13107a27283
> "0080548","LEOPARD syndrome 1","omim","151100"
13108a27285
> "0080326","familial hypertrophic cardiomyopathy","omim","192600"
13109a27287,27288
> "14737","craniofrontonasal syndrome","omim","304110"
> "0080273","polycystic kidney disease 5","omim","617610"
13111c27290,27294
< "0050779","hydrolethalus syndrome","omim","236680"
---
> "0111355","hydrolethalus syndrome 1","omim","236680"
> "0070217","familial hyperinsulinemic hypoglycemia 6","omim","606762"
> "0060280","primary pigmented nodular adrenocortical disease","omim","610489"
> "0111561","stiff skin syndrome","omim","184900"
> "1339","Diamond-Blackfan anemia","omim","613308"
13113c27296
< "0060867","macrocephaly-autism syndrome","omim","605309"
---
> "0050469","Costello syndrome","omim","218040"
13117a27301,27303
> "0070061","autosomal dominant non-syndromic intellectual disability 31","omim","616158"
> "0110819","hereditary spastic paraplegia 74","omim","616451"
> "0110971","brachydactyly type D","omim","113200"
13119c27305
< "0060911","karyomegalic interstitial nephritis","omim","614817"
---
> "0060416","chromosome 2q31.2 deletion syndrome","omim","612345"
13121c27307,27309
< "0110987","Joubert syndrome 18","omim","614815"
---
> "2842","Jervell-Lange Nielsen syndrome","omim","612347"
> "0111325","juvenile myoclonic epilepsy 10","omim","617924"
> "14768","Saethre-Chotzen syndrome","omim","101400"
13122a27311,27312
> "0090040","torsion dystonia 7","omim","602124"
> "0060447","epithelial basement membrane dystrophy","omim","121820"
13124,13125c27314,27320
< "0110339","osteogenesis imperfecta type 3","omim","259420"
< "0060582","Noonan syndrome 4","omim","610733"
---
> "0110317","hypertrophic cardiomyopathy 11","omim","612098"
> "1094","attention deficit hyperactivity disorder","omim","612312"
> "0110626","primary ciliary dyskinesia 2","omim","606763"
> "0080440","early infantile epileptic encephalopathy 3","omim","609304"
> "0050975","spinocerebellar ataxia type 26","omim","609306"
> "0050976","spinocerebellar ataxia type 27","omim","609307"
> "0080442","early infantile epileptic encephalopathy 41","omim","617105"
13127,13129c27322,27332
< "5426","premature ovarian failure","omim","612310"
< "0110433","dilated cardiomyopathy 1E","omim","601154"
< "0050535","exudative vitreoretinopathy","omim","305390"
---
> "0080454","early infantile epileptic encephalopathy 42","omim","617106"
> "10908","hydrocephalus","omim","615219"
> "0080412","familial adenomatous polyposis 4","omim","617100"
> "9563","bronchiectasis","omim","211400"
> "0080324","tuberous sclerosis 1","omim","191100"
> "0050453","lissencephaly","omim","611603"
> "0111255","McKusick-Kaufman syndrome","omim","236700"
> "0111413","X-linked exudative vitreoretinopathy 2","omim","305390"
> "0110756","type 1 diabetes mellitus 19","omim","610155"
> "2736","Hajdu-Cheney syndrome","omim","102500"
> "0110070","arrhythmogenic right ventricular dysplasia 1","omim","107970"
13136d27338
< "0090025","split hand-foot malformation 3","omim","246560"
13137a27340
> "0080345","blepharocheilodontic syndrome 1","omim","119580"
13139,13140c27342,27343
< "0110282","autosomal recessive limb-girdle muscular dystrophy type 2H","omim","254110"
< "0110416","retinitis pigmentosa 24","omim","300155"
---
> "0070232","benign recurrent intrahepatic cholestasis 2","omim","605479"
> "0050690","brachyolmia","omim","113500"
13142a27346
> "0111277","mitochondrial trifunctional protein deficiency","omim","609015"
13143a27348
> "0111205","distal hereditary motor neuronopathy type 5B","omim","614751"
13152c27357
< "14448","46 XY gonadal dysgenesis","omim","613762"
---
> "0110596","primary ciliary dyskinesia 21","omim","615294"
13155c27360
< "0110402","retinitis pigmentosa 45","omim","613767"
---
> "0050468","yellow nail syndrome","omim","153300"
13157c27362,27364
< "9406","hypopituitarism","omim","262700"
---
> "0110230","cataract 34 multiple types","omim","612968"
> "0060289","Ohdo syndrome","omim","249620"
> "0111591","congenital heart defects, hamartomas of tongue, and polysyndactyly","omim","217085"
13161a27369,27370
> "0060462","Desbuquois dysplasia","omim","615777"
> "0111498","combined oxidative phosphorylation deficiency 22","omim","616045"
13163c27372,27373
< "0050650","familial atrial fibrillation","omim","615770"
---
> "0070219","familial hyperinsulinemic hypoglycemia 1","omim","256450"
> "0080571","congenital disorder of glycosylation Iu","omim","615042"
13165a27376,27377
> "0090136","complex cortical dysplasia with other brain malformations 6","omim","615771"
> "9884","muscular dystrophy","omim","310095"
13166a27379
> "0110754","type 1 diabetes mellitus 17","omim","603266"
13167a27381
> "0110497","autosomal recessive nonsyndromic deafness 39","omim","608265"
13171c27385,27386
< "0050881","inclusion body myopathy with Paget disease of bone and frontotemporal dementia","omim","167320"
---
> "1540","parathyroid carcinoma","omim","608266"
> "3132","porphyria cutanea tarda","omim","176090"
13172a27388
> "14748","Sotos syndrome","omim","614753"
13175c27391
< "0110230","cataract 34 multiple types","omim","612968"
---
> "0080109","infantile myofibromatosis","omim","615293"
13177,13178c27393,27395
< "14448","46 XY gonadal dysgenesis","omim","612965"
< "13099","Moyamoya disease","omim","300845"
---
> "0110086","asphyxiating thoracic dystrophy 2","omim","611263"
> "0050794","multiple synostoses syndrome","omim","612961"
> "0110605","primary ciliary dyskinesia 7","omim","611884"
13180c27397,27398
< "0050799","guanidinoacetate methyltransferase deficiency","omim","612736"
---
> "4751","striatonigral degeneration","omim","609161"
> "0060587","Noonan syndrome 9","omim","616559"
13183c27401,27402
< "12800","mucopolysaccharidosis VI","omim","253200"
---
> "0050710","3-Methylcrotonyl-CoA carboxylase deficiency","omim","210200"
> "0111027","hemochromatosis type 2A","omim","602390"
13185a27405,27406
> "0110119","autoimmune lymphoproliferative syndrome type 3","omim","615559"
> "11589","Riley-Day syndrome","omim","223900"
13187c27408,27409
< "0070037","autosomal dominant non-syndromic intellectual disability 7","omim","614104"
---
> "9620","vesicoureteral reflux","omim","314550"
> "0060262","gallbladder disease","omim","611465"
13188a27411
> "0111215","distal hereditary motor neuronopathy type 8","omim","600175"
13190c27413,27414
< "0111125","nephronophthisis 18","omim","615862"
---
> "2977","primary hyperoxaluria","omim","613616"
> "0050577","Sensenbrenner syndrome","omim","613610"
13192a27417,27418
> "0111530","linear nevus sebaceous syndrome","omim","163200"
> "0110824","hereditary spastic paraplegia 9A","omim","601162"
13195a27422,27423
> "12120","pulmonary alveolar proteinosis","omim","300770"
> "83","cataract","omim","601371"
13197c27425
< "0110848","xeroderma pigmentosum group F","omim","278760"
---
> "0050432","Asperger syndrome","omim","608781"
13199c27427
< "3687","MELAS syndrome","omim","540000"
---
> "0110698","hypotrichosis 1","omim","605389"
13200a27429
> "0111452","progressive myoclonus epilepsy 1A","omim","254800"
13201a27431
> "0050792","multiple cutaneous and mucosal venous malformations","omim","600195"
13203a27434,27436
> "12169","carpal tunnel syndrome","omim","115430"
> "0111297","familial febrile seizures","omim","121210"
> "0060165","Kleine-Levin syndrome","omim","148840"
13206,13209c27439,27453
< "0060754","familial temporal lobe epilepsy 8","omim","616461"
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","614249"
< "0060369","autosomal recessive early-onset Parkinson's disease 6","omim","605909"
< "14717","centronuclear myopathy","omim","160150"
---
> "13481","thanatophoric dysplasia","omim","187600"
> "13481","thanatophoric dysplasia","omim","187601"
> "0080038","pycnodysostosis","omim","265800"
> "1838","Menkes disease","omim","309400"
> "0111567","retinal vasculopathy with cerebral leukodystrophy","omim","192315"
> "0050959","spinocerebellar ataxia type 8","omim","608768"
> "4279","infundibulocystic basal cell carcinoma","omim","604451"
> "0060369","Parkinson's disease 6","omim","605909"
> "14415","Legg-Calve-Perthes disease","omim","150600"
> "14557","primary pulmonary hypertension","omim","615344"
> "0111584","dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","omim","212112"
> "0111223","centronuclear myopathy 1","omim","160150"
> "0080074","neural tube defect","omim","301410"
> "14557","primary pulmonary hypertension","omim","615342"
> "13922","eosinophilic esophagitis","omim","610247"
13211c27455,27456
< "14670","hypertelorism, microtia, facial clefting syndrome","omim","239800"
---
> "0110115","autoimmune lymphoproliferative syndrome type 2A","omim","603909"
> "0050802","Ehlers-Danlos syndrome progeroid type","omim","615349"
13214c27459,27462
< "5684","spondyloepimetaphyseal dysplasia, Sponastrime type","omim","271510"
---
> "8943","lattice corneal dystrophy","omim","122200"
> "0050982","spinocerebellar ataxia type 35","omim","613908"
> "0050973","spinocerebellar ataxia type 23","omim","610245"
> "0110848","xeroderma pigmentosum group F","omim","278760"
13216c27464
< "0060682","autosomal dominant nocturnal frontal lobe epilepsy 1","omim","600513"
---
> "0080493","ovarian dysgenesis 1","omim","233300"
13219c27467,27468
< "2476","hereditary spastic paraplegia","omim","303350"
---
> "8997","polycythemia vera","omim","263300"
> "0060882","renal hypomagnesemia 4","omim","611718"
13222c27471,27475
< "12783","migraine without aura","omim","607501"
---
> "0080175","cloacal exstrophy","omim","258040"
> "0111456","Kaufman oculocerebrofacial syndrome","omim","244450"
> "0050882","spinocerebellar ataxia type 5","omim","600224"
> "1588","thrombocytopenia","omim","188000"
> "0060261","congenital ptosis","omim","178300"
13224a27478
> "0111390","mucopolysaccharidosis Ih","omim","607014"
13227c27481,27482
< "0110486","autosomal recessive nonsyndromic deafness 28","omim","609823"
---
> "0050434","Andersen-Tawil syndrome","omim","170390"
> "2582","acatalasia","omim","614097"
13228a27484
> "6686","Achard syndrome","omim","100700"
13232,13233c27488,27490
< "9620","vesicoureteral reflux","omim","314550"
< "0111073","progressive familial heart block","omim","113900"
---
> "0070037","autosomal dominant non-syndromic intellectual disability 7","omim","614104"
> "0110226","Brugada syndrome 9","omim","616399"
> "0110370","retinitis pigmentosa 55","omim","613575"
13235c27492,27493
< "0110079","Leber congenital amaurosis 8","omim","613835"
---
> "0080141","mosaic variegated aneuploidy syndrome 1","omim","257300"
> "0111358","Floating-Harbor syndrome","omim","136140"
13237c27495
< "0090104","Huntington's disease-like 2","omim","606438"
---
> "0080471","infantile or early childhood epileptic encephalopathy 2","omim","617829"
13239c27497,27500
< "0070124","congenital nongoitrous hypothyroidism 2","omim","218700"
---
> "0050453","lissencephaly","omim","607432"
> "0111257","gamma-glutamyl transpeptidase deficiency","omim","231950"
> "0111555","Alkuraya-Kucinskas syndrome","omim","617822"
> "0111369","hyperalphalipoproteinemia 1","omim","143470"
13241c27502
< "3969","papillary thyroid carcinoma","omim","188550"
---
> "3969","thyroid gland papillary carcinoma","omim","188550"
13246a27508
> "0110274","autosomal recessive limb-girdle muscular dystrophy","omim","253600"
13248a27511
> "0060346","Native American myopathy","omim","255995"
13249a27513
> "0080504","Parkinson's disease 22","omim","616710"
13251c27515
< "0050577","Sensenbrenner syndrome","omim","613610"
---
> "0060161","Kennedy's disease","omim","313200"
13252a27517
> "0060353","acrofacial dysostosis Cincinnati type","omim","616462"
13254,13257c27519,27526
< "0060228","intracranial berry aneurysm","omim","612161"
< "0050425","restless legs syndrome","omim","615197"
< "0070022","autosomal recessive dyskeratosis congenita 5","omim","615190"
< "0111053","platelet-type bleeding disorder 15","omim","615193"
---
> "0080540","galactosialidosis","omim","256540"
> "0050970","spinocerebellar ataxia type 19/22","omim","607346"
> "0090042","torsion dystonia 17","omim","612406"
> "10487","Hirschsprung's disease","omim","608462"
> "6406","double outlet right ventricle","omim","217095"
> "0060556","Kufor-Rakeb syndrome","omim","606693"
> "0050453","lissencephaly","omim","615191"
> "3319","lymphangioleiomyomatosis","omim","606690"
13259a27529,27530
> "310","MERRF syndrome","omim","545000"
> "9266","cystinuria","omim","220100"
13262,13263c27533,27535
< "0110510","autosomal recessive nonsyndromic deafness 55","omim","609952"
< "0110395","retinitis pigmentosa 72","omim","616469"
---
> "0050801","androgenic alopecia","omim","300710"
> "14503","neuronal ceroid lipofuscinosis","omim","256730"
> "0110146","Bartter disease type 4b","omim","613090"
13265c27537
< "0060370","autosomal recessive early-onset Parkinson's disease 7","omim","606324"
---
> "0060370","Parkinson's disease 7","omim","606324"
13267,13270c27539,27543
< "0070230","benign recurrent intrahepatic cholestasis","omim","243300"
< "0050425","restless legs syndrome","omim","611185"
< "0050469","Costello syndrome","omim","218040"
< "8923","skin melanoma","omim","608035"
---
> "0060228","intracranial berry aneurysm","omim","612162"
> "14683","Binder syndrome","omim","155050"
> "0060549","Barber-Say syndrome","omim","209885"
> "0110894","inflammatory bowel disease 11","omim","191390"
> "0070260","congenital disorder of glycosylation type IIh","omim","611182"
13272,13273c27545,27547
< "13533","osteopetrosis","omim","259700"
< "0110529","autosomal recessive nonsyndromic deafness 84A","omim","613391"
---
> "0110420","dominant pericentral pigmentary retinopathy","omim","180210"
> "0111209","distal hereditary motor neuronopathy type 2C","omim","613376"
> "0060174","GABA aminotransferase deficiency","omim","613163"
13274a27549
> "0080463","early infantile epileptic encephalopathy 33","omim","616409"
13279a27555,27556
> "1324","lung cancer","omim","612571"
> "0050629","Aicardi-Goutieres syndrome","omim","610181"
13280a27558
> "0060407","chromosome 18q deletion syndrome","omim","601808"
13283c27561
< "0060649","congenital hereditary endothelial dystrophy of cornea","omim","217700"
---
> "0060228","intracranial berry aneurysm","omim","612161"
13286c27564,27566
< "0110924","familial hemophagocytic lymphohistiocytosis 4","omim","603552"
---
> "0111108","maturity-onset diabetes of the young type 10","omim","613370"
> "0111388","X-linked hypoparathyroidism","omim","307700"
> "0050474","Netherton syndrome","omim","256500"
13288c27568
< "0080327","multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly","omim","236500"
---
> "0110388","retinitis pigmentosa 10","omim","180105"
13291a27572
> "0060304","dyschromatosis universalis hereditaria","omim","127500"
13294c27575
< "14748","Sotos syndrome","omim","614753"
---
> "14289","Ebstein anomaly","omim","224700"
13297c27578,27580
< "0080209","sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay","omim","616084"
---
> "0050998","nonprogressive cerebellar ataxia with mental retardation","omim","614756"
> "11949","Creutzfeldt-Jakob disease","omim","123400"
> "0111550","scalp-ear-nipple syndrome","omim","181270"
13299c27582
< "12177","common variable immunodeficiency","omim","240500"
---
> "9273","citrullinemia","omim","215700"
13300a27584
> "12132","granulomatosis with polyangiitis","omim","608710"
13303c27587,27588
< "0050965","spinocerebellar ataxia type 15","omim","606658"
---
> "0080283","early infantile epileptic encephalopathy 55","omim","617599"
> "11555","Fuchs' endothelial dystrophy","omim","613271"
13307c27592
< "0110214","cleft soft palate","omim","119570"
---
> "0050776","non-syndromic X-linked intellectual disability","omim","300387"
13310a27596,27597
> "0060288","omodysplasia","omim","258315"
> "0080530","granular corneal dystrophy 1","omim","121900"
13314c27601,27603
< "2224","essential thrombocythemia","omim","601977"
---
> "0111410","exudative vitreoretinopathy 6","omim","616468"
> "0110488","autosomal recessive nonsyndromic deafness 3","omim","600316"
> "0050465","Muir-Torre syndrome","omim","158320"
13315a27605,27608
> "0110546","autosomal dominant nonsyndromic deafness 15","omim","602459"
> "0080315","megalencephalic leukoencephalopathy with subcortical cysts","omim","604004"
> "11353","bladder diverticulum","omim","109820"
> "0111484","combined oxidative phosphorylation deficiency 18","omim","615578"
13316a27610
> "11342","arcus senilis","omim","107800"
13318c27612,27613
< "0110220","Brugada syndrome 3","omim","611875"
---
> "0070145","hereditary sensory and autonomic neuropathy type 5","omim","608654"
> "0080391","nephrotic syndrome type 9","omim","615573"
13322a27618,27620
> "0111210","distal hereditary motor neuronopathy type 2D","omim","615575"
> "0050559","Fukuyama congenital muscular dystrophy","omim","253800"
> "0080280","gingival fibromatosis 5","omim","617626"
13324c27622
< "12603","acute leukemia","omim","308960"
---
> "0110400","retinitis pigmentosa 22","omim","602594"
13327c27625
< "0110608","primary ciliary dyskinesia 19","omim","614935"
---
> "0110405","retinitis pigmentosa 36","omim","610599"
13329,13330c27627,27630
< "0060234","Carpenter syndrome","omim","614976"
< "891","progressive myoclonus epilepsy","omim","611726"
---
> "0111330","combined saposin deficiency","omim","611721"
> "0070090","schizophrenia 14","omim","612361"
> "0080281","schizophrenia 19","omim","617629"
> "0111467","combined oxidative phosphorylation deficiency 13","omim","614932"
13331a27632,27633
> "0111444","progressive myoclonus epilepsy 4","omim","254900"
> "3204","neurilemmomatosis","omim","162091"
13337,13338c27639,27640
< "0110575","autosomal dominant nonsyndromic deafness 5","omim","600994"
< "9074","systemic lupus erythematosus","omim","605480"
---
> "0050578","occult macular dystrophy","omim","613587"
> "0050451","Brugada syndrome","omim","601144"
13342a27645,27649
> "1588","thrombocytopenia","omim","612004"
> "0080030","spondyloepimetaphyseal dysplasia, Missouri type","omim","602111"
> "0080435","early infantile epileptic encephalopathy 37","omim","616981"
> "14452","hypokalemic periodic paralysis","omim","613345"
> "0111549","aplasia of lacrimal and salivary glands","omim","180920"
13345c27652,27654
< "0060804","syndromic X-linked intellectual disability 12","omim","309545"
---
> "0111391","mucopolysaccharidosis IVA","omim","253000"
> "4428","dyslexia","omim","608995"
> "0060304","dyschromatosis universalis hereditaria","omim","615402"
13347c27656,27657
< "14717","centronuclear myopathy","omim","614807"
---
> "0111224","centronuclear myopathy 4","omim","614807"
> "0060019","coronin-1A deficiency","omim","615401"
13350a27661
> "0111363","Heinz body anemia","omim","140700"
13353a27665,27668
> "0111185","myopathy, lactic acidosis, and sideroblastic anemia 1","omim","600462"
> "0080499","ovarian dysgenesis 7","omim","618117"
> "0111227","chromosome 3-linked frontotemporal dementia","omim","600795"
> "0111318","idiopathic generalized epilepsy 3","omim","608762"
13356c27671,27675
< "0050646","distal arthrogryposis","omim","121050"
---
> "13714","anodontia","omim","206780"
> "13099","Moyamoya disease","omim","300845"
> "0080424","early infantile epileptic encephalopathy 44","omim","617132"
> "10608","celiac disease","omim","609754"
> "0110973","Mononen-Karnes-Senac syndrome","omim","301940"
13358,13362c27677,27682
< "3156","hypomelanosis of Ito","omim","300337"
< "417","autoimmune hypersensitivity disease","omim","109100"
< "0060464","Feingold syndrome","omim","614326"
< "10629","microphthalmia","omim","300166"
< "2340","craniosynostosis","omim","182212"
---
> "0111182","familial hemiplegic migraine 2","omim","602481"
> "0070207","familial partial lipodystrophy type 1","omim","608600"
> "0070131","autosomal dominant cutis laxa 3","omim","616603"
> "11830","myopia","omim","609259"
> "0060334","transient neonatal diabetes mellitus","omim","610582"
> "0070186","Y-linked spermatogenic failure 1","omim","400042"
13368,13372c27688,27692
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","611097"
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","611096"
< "4279","infundibulocystic basal cell carcinoma","omim","604451"
< "0070249","autosomal dominant Emery-Dreifuss muscular dystrophy 4","omim","612998"
< "0090117","thiamine-responsive megaloblastic anemia syndrome","omim","249270"
---
> "0060296","congenital secretory chloride diarrhea 1","omim","214700"
> "1588","thrombocytopenia","omim","300367"
> "4400","dermatosis papulosa nigra","omim","125600"
> "0070264","congenital disorder of glycosylation type IIl","omim","614576"
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","614249"
13375a27696
> "7400","Nijmegen breakage syndrome","omim","251260"
13377,13378c27698
< "3210","Pelizaeus-Merzbacher disease","omim","312080"
< "0110494","autosomal recessive nonsyndromic deafness 36","omim","609006"
---
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","611093"
13380a27701,27702
> "10017","multiple endocrine neoplasia type 1","omim","131100"
> "0050659","biotin-responsive basal ganglia disease","omim","607483"
13386c27708,27709
< "0060805","Prieto syndrome","omim","309610"
---
> "11819","ureter cancer","omim","191600"
> "0070196","infantile-onset distal myopathy","omim","160300"
13388c27711
< "0110018","age related macular degeneration 6","omim","613757"
---
> "0060335","autosomal dominant sideroblastic anemia 4","omim","182170"
13394,13395c27717,27719
< "9220","central sleep apnea","omim","107640"
< "0110311","hypertrophic cardiomyopathy 21","omim","614676"
---
> "0110328","hypertrophic cardiomyopathy 25","omim","607487"
> "0110588","autosomal dominant nonsyndromic deafness 67","omim","616340"
> "0060438","Cole-Carpenter syndrome","omim","112240"
13397c27721,27722
< "0060483","MEDNIK syndrome","omim","609313"
---
> "0060213","FTDALS1","omim","105550"
> "0080129","mitochondrial DNA depletion syndrome 11","omim","615084"
13399c27724
< "0070274","hereditary nonpolyposis colorectal cancer type 2","omim","609310"
---
> "0050328","congenital hypothyroidism","omim","275200"
13402c27727
< "0110824","hereditary spastic paraplegia 9A","omim","601162"
---
> "0110141","Bardet-Biedl syndrome 19","omim","615996"
13405c27730
< "0110136","Bardet-Biedl syndrome 14","omim","615991"
---
> "6255","growth hormone secreting pituitary adenoma","omim","102200"
13411c27736,27738
< "288","endometriosis of uterus","omim","600458"
---
> "0080398","orofacial cleft 4","omim","608371"
> "13774","Addison's disease","omim","240200"
> "1062","Fanconi syndrome","omim","615605"
13413c27740,27741
< "0050802","Ehlers-Danlos syndrome progeroid type","omim","615349"
---
> "0111149","autosomal recessive isolated ectopia lentis 2","omim","225100"
> "0111189","distal muscular dystrophy 3","omim","610099"
13414a27743,27744
> "0110236","cataract 39 multiple types","omim","615188"
> "0080505","Cornelia de Lange syndrome 1","omim","122470"
13416c27746,27747
< "10629","microphthalmia","omim","615972"
---
> "0080064","autosomal recessive spinocerebellar ataxia 17","omim","616127"
> "0080108","myoglobinuria","omim","160010"
13419c27750,27754
< "7148","rheumatoid arthritis","omim","180300"
---
> "0111577","dehydrated hereditary stomatocytosis 2","omim","616689"
> "0050887","Townes-Brocks syndrome","omim","107480"
> "0080070","inclusion-cell disease","omim","252500"
> "0110866","congenital stationary night blindness 1H","omim","617024"
> "2224","essential thrombocythemia","omim","601977"
13421c27756,27757
< "1702","ichthyosis vulgaris","omim","146700"
---
> "0111472","combined oxidative phosphorylation deficiency 9","omim","614582"
> "0080142","mosaic variegated aneuploidy syndrome 2","omim","614114"
13422a27759
> "11202","primary hyperparathyroidism","omim","600166"
13424c27761
< "0110926","nemaline myopathy 1","omim","609284"
---
> "0060839","isolated microphthalmia 2","omim","610093"
13426c27763,27764
< "0090007","immunodeficiency-centromeric instability-facial anomalies syndrome","omim","242860"
---
> "0111315","idiopathic generalized epilepsy 14","omim","616685"
> "0111582","hereditary arterial and articular multiple calcification syndrome","omim","211800"
13428a27767,27768
> "10908","hydrocephalus","omim","236600"
> "0111541","pigmented paravenous chorioretinal atrophy","omim","172870"
13431a27772
> "12642","hiatus hernia","omim","142400"
13432a27774
> "0050854","Muckle-Wells syndrome","omim","191900"
13433a27776,27777
> "0060539","Hermansky-Pudlak syndrome 1","omim","203300"
> "0060682","autosomal dominant nocturnal frontal lobe epilepsy 1","omim","600513"
13436a27781
> "13910","red color blindness","omim","303900"
13437a27783,27785
> "0050589","inflammatory bowel disease","omim","266600"
> "0050648","atelosteogenesis","omim","256050"
> "1172","hyperlipoproteinemia type IV","omim","144600"
13442c27790,27791
< "8997","polycythemia vera","omim","263300"
---
> "0070329","mitochondrial DNA depletion syndrome","omim","603041"
> "0080290","familial erythrocytosis 5","omim","617907"
13444,13445c27793,27794
< "2058","chronic mucocutaneous candidiasis","omim","607644"
< "0060733","junctional epidermolysis bullosa with pyloric atresia","omim","226730"
---
> "0050568","spondylocostal dysostosis","omim","608681"
> "0050971","spinocerebellar ataxia type 20","omim","608687"
13451c27800,27802
< "0080173","bladder exstrophy-epispadias-cloacal exstrophy complex","omim","258040"
---
> "0111450","progressive myoclonus epilepsy 9","omim","616540"
> "9649","congenital nystagmus","omim","164100"
> "0060021","DNA ligase IV deficiency","omim","606593"
13453c27804,27810
< "0110569","autosomal dominant nonsyndromic deafness 44","omim","607453"
---
> "0110549","autosomal dominant nonsyndromic deafness 18","omim","606012"
> "0090046","dystonia 21","omim","614588"
> "0050661","vitelliform macular dystrophy","omim","616151"
> "0080333","aortic valve disease 1","omim","109730"
> "0050438","Frasier syndrome","omim","136680"
> "0111213","distal spinal muscular atrophy type 4","omim","611067"
> "0110078","Leber congenital amaurosis 1","omim","204000"
13455a27813
> "0111418","familial apolipoprotein C-II deficiency","omim","207750"
13457c27815
< "0110586","autosomal dominant nonsyndromic deafness 65","omim","616044"
---
> "0050754","ataxia with oculomotor apraxia type 1","omim","208920"
13465,13466c27823,27824
< "0070250","autosomal dominant Emery-Dreifuss muscular dystrophy 5","omim","612999"
< "0110086","asphyxiating thoracic dystrophy 2","omim","611263"
---
> "0050763","ARC syndrome","omim","208085"
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","614343"
13468c27826,27827
< "0110876","holoprosencephaly 7","omim","610828"
---
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","614341"
> "0080513","Meier-Gorlin syndrome 2","omim","613800"
13470c27829,27833
< "0070238","primary coenzyme Q10 deficiency 1","omim","607426"
---
> "0050387","nonpapillary renal cell carcinoma","omim","144700"
> "0080514","Meier-Gorlin syndrome 3","omim","613803"
> "0080515","Meier-Gorlin syndrome 4","omim","613804"
> "0080516","Meier-Gorlin syndrome 5","omim","613805"
> "0060643","primary sclerosing cholangitis","omim","613806"
13472,13473c27835,27836
< "0110623","primary ciliary dyskinesia 15","omim","613808"
< "0110360","retinitis pigmentosa 39","omim","613809"
---
> "0080227","autosomal dominant mental retardation 55","omim","617831"
> "0080285","early infantile epileptic encephalopathy 58","omim","617830"
13474a27838
> "0080473","developmental delay and seizures with or without movement abnormalities","omim","617836"
13478a27843
> "0111436","optic atrophy 11","omim","617302"
13482c27847
< "2231","factor XII deficiency","omim","234000"
---
> "0110965","brachydactyly type A2","omim","112600"
13484a27850,27851
> "0080431","early infantile epileptic encephalopathy 19","omim","615744"
> "0110355","retinitis pigmentosa 32","omim","609913"
13486a27854,27855
> "350","mastocytosis","omim","154800"
> "11830","myopia","omim","608908"
13489c27858
< "0050588","muscular dystrophy-dystroglycanopathy","omim","615181"
---
> "0111230","congenital muscular dystrophy-dystroglycanopathy type A11","omim","615181"
13493c27862
< "0110236","cataract 39 multiple types","omim","615188"
---
> "0090006","renal coloboma syndrome","omim","120330"
13495c27864
< "0050434","Andersen-Tawil syndrome","omim","170390"
---
> "2988","antiphospholipid syndrome","omim","107320"
13498c27867,27868
< "5425","ovarian hyperstimulation syndrome","omim","608115"
---
> "12120","pulmonary alveolar proteinosis","omim","610913"
> "0060708","lymphoproliferative syndrome 2","omim","615122"
13500c27870,27871
< "6688","autoimmune lymphoproliferative syndrome","omim","601859"
---
> "1094","attention deficit hyperactivity disorder","omim","608904"
> "0111196","X-linked distal spinal muscular atrophy 3","omim","300489"
13502c27873,27875
< "1094","attention deficit hyperactivity disorder","omim","608906"
---
> "0090102","autosomal dominant macrothrombocytopenia TUBB1-related","omim","613112"
> "0060199","amyotrophic lateral sclerosis type 7","omim","608031"
> "6678","tooth and nail syndrome","omim","189500"
13503a27877,27878
> "0111543","juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome","omim","175050"
> "0111105","maturity-onset diabetes of the young type 8","omim","609812"
13505c27880
< "0050650","familial atrial fibrillation","omim","612201"
---
> "0111062","familial hypobetalipoproteinemia 1","omim","615558"
13512c27887,27888
< "13359","Ehlers-Danlos syndrome","omim","130000"
---
> "0060280","primary pigmented nodular adrenocortical disease","omim","615830"
> "0110872","holoprosencephaly 2","omim","157170"
13514a27891
> "0050472","monilethrix","omim","158000"
13515a27893
> "2452","thrombophilia","omim","188050"
13516a27895,27896
> "12731","pars planitis","omim","606177"
> "0060646","congenital chylothorax","omim","603523"
13526c27906,27907
< "13945","CADASIL","omim","125310"
---
> "0070160","atypical hereditary sensory neuropathy","omim","256860"
> "2861","congenital nonspherocytic hemolytic anemia","omim","206400"
13528a27910
> "0080331","cold-induced sweating syndrome 3","omim","617055"
13530,13532c27912,27916
< "0110590","autosomal dominant nonsyndromic deafness 69","omim","616697"
< "0110809","hereditary spastic paraplegia 57","omim","615658"
< "0050664","Bietti crystalline corneoretinal dystrophy","omim","210370"
---
> "0080342","Simpson-Golabi-Behmel syndrome type 2","omim","300209"
> "14789","spondyloepiphyseal dysplasia congenita","omim","183900"
> "0060367","Parkinson's disease 1","omim","168601"
> "0110023","age related macular degeneration 11","omim","611953"
> "8552","chronic myeloid leukemia","omim","608232"
13533a27918
> "0111030","hemochromatosis type 3","omim","604250"
13535a27921,27924
> "0050986","spinocerebellar ataxia type 40","omim","616053"
> "0050755","ataxia with oculomotor apraxia type 2","omim","606002"
> "0050996","episodic ataxia type 8","omim","616055"
> "0080461","early infantile epileptic encephalopathy 26","omim","616056"
13536a27926
> "0060408","chromosome 19q13.11 deletion syndrome","omim","613026"
13538,13539c27928,27932
< "0080068","Charcot-Marie-Tooth disease type 6","omim","616505"
< "9563","bronchiectasis","omim","613021"
---
> "0070089","schizophrenia 13","omim","613025"
> "0080259","autosomal recessive spinocerebellar ataxia 25","omim","617584"
> "0080359","fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3","omim","616500"
> "0080527","bronchiectasis 2","omim","613021"
> "0080550","LEOPARD syndrome 3","omim","613707"
13542c27935
< "0060025","immunoglobulin alpha deficiency","omim","609529"
---
> "3369","Ewing sarcoma","omim","612219"
13544c27937,27938
< "0060472","Kindler syndrome","omim","173650"
---
> "0080353","X-linked recessive hypophosphatemic rickets","omim","300554"
> "2987","familial Mediterranean fever","omim","249100"
13546c27940,27943
< "8986","narcolepsy","omim","609039"
---
> "12388","neurohypophyseal diabetes insipidus","omim","304900"
> "9467","nail-patella syndrome","omim","161200"
> "12603","acute leukemia","omim","308960"
> "0060838","isolated microphthalmia 7","omim","613704"
13548,13549c27945,27947
< "1657","ventricular septal defect","omim","614431"
< "0110605","primary ciliary dyskinesia 7","omim","611884"
---
> "0080496","ovarian dysgenesis 4","omim","616185"
> "0111262","infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly","omim","613668"
> "0080082","nonsyndromic congenital nail disorder 4","omim","206800"
13551c27949
< "0110359","retinitis pigmentosa 67","omim","615565"
---
> "0060485","Mowat-Wilson syndrome","omim","235730"
13553a27952
> "0080260","autosomal recessive spinocerebellar ataxia 26","omim","617633"
13554a27954,27955
> "0080261","autosomal recessive nonsyndromic deafness 106","omim","617637"
> "0080238","autosomal dominant mental retardation 47","omim","617635"
13556a27958,27960
> "0111507","Lenz-Majewski hyperostotic dwarfism","omim","151050"
> "0080262","autosomal recessive nonsyndromic deafness 107","omim","617639"
> "0080216","duodenal atresia","omim","223400"
13558c27962,27964
< "0050678","Blau syndrome","omim","186580"
---
> "0110169","Charcot-Marie-Tooth disease axonal type 2P","omim","614436"
> "14448","46 XY gonadal dysgenesis","omim","612965"
> "11211","buphthalmos","omim","231300"
13559a27966,27967
> "0090031","D-bifunctional protein deficiency","omim","261515"
> "0111437","optic atrophy 7","omim","612989"
13561a27970
> "0110133","Bardet-Biedl syndrome 11","omim","615988"
13567c27976,27977
< "0090128","dilated cardiomyopathy with woolly hair and keratoderma","omim","605676"
---
> "0070022","autosomal recessive dyskeratosis congenita 5","omim","615190"
> "0090128","Carvajal syndrome","omim","605676"
13570c27980
< "6457","Cowden syndrome","omim","158350"
---
> "0090104","Huntington's disease-like 2","omim","606438"
13574a27985
> "0060456","Schnyder corneal dystrophy","omim","121800"
13577c27988,27989
< "0050588","muscular dystrophy-dystroglycanopathy","omim","614830"
---
> "0090074","hypogonadotropic hypogonadism 8 with or without anosmia","omim","614837"
> "0111231","congenital muscular dystrophy-dystroglycanopathy type A8","omim","614830"
13579a27992,27995
> "0050679","blue cone monochromacy","omim","303700"
> "0070124","congenital nongoitrous hypothyroidism 2","omim","218700"
> "11633","thyroid hormone resistance syndrome","omim","274300"
> "0111367","Beukes hip dysplasia","omim","142669"
13581a27998
> "0110525","autosomal recessive nonsyndromic deafness 77","omim","613079"
13583c28000,28001
< "0110672","congenital myasthenic syndrome 21","omim","617239"
---
> "0050715","methylmalonic aciduria and homocystinuria type cblC","omim","277400"
> "0060811","syndromic X-linked intellectual disability Turner type","omim","309590"
13585,13587c28003,28006
< "2120","focal dermal hypoplasia","omim","305600"
< "0111129","focal segmental glomerulosclerosis 2","omim","603965"
< "2571","Langerhans-cell histiocytosis","omim","604856"
---
> "0050424","familial adenomatous polyposis","omim","175100"
> "0110156","Charcot-Marie-Tooth disease type 2B1","omim","605588"
> "0070011","Seckel syndrome 7","omim","614851"
> "0090025","split hand-foot malformation 3","omim","246560"
13589a28009
> "3613","Canavan disease","omim","271900"
13592c28012,28013
< "0110405","retinitis pigmentosa 36","omim","610599"
---
> "4465","papillary renal cell carcinoma","omim","605074"
> "0050692","Brody myopathy","omim","601003"
13593a28015,28019
> "0111545","familial male-limited precocious puberty","omim","176410"
> "0060347","acrorenal syndrome","omim","102520"
> "0060173","Timothy syndrome","omim","601005"
> "9883","Becker muscular dystrophy","omim","300376"
> "0111430","essential tremor 3","omim","611456"
13595c28021
< "3393","coronary artery disease","omim","612030"
---
> "0050646","distal arthrogryposis","omim","193700"
13596a28023
> "0111486","combined oxidative phosphorylation deficiency 3","omim","610505"
13598c28025,28029
< "0070071","autosomal dominant non-syndromic intellectual disability 41","omim","616944"
---
> "0070152","hereditary sensory and autonomic neuropathy type 1A","omim","162400"
> "14671","multiple intestinal atresia","omim","243150"
> "0111053","platelet-type bleeding disorder 15","omim","615193"
> "0111570","snowflake vitreoretinal degeneration","omim","193230"
> "0110628","primary ciliary dyskinesia 24","omim","615481"
13599a28031,28032
> "0080120","mitochondrial DNA depletion syndrome 2","omim","609560"
> "0111531","bilateral optic nerve hypoplasia","omim","165550"
13601c28034,28038
< "0050644","arterial calcification of infancy","omim","208000"
---
> "0110933","nemaline myopathy 11","omim","617336"
> "0111270","isolated sulfite oxidase deficiency","omim","272300"
> "0111560","Charcot-Marie-Tooth disease type 1G","omim","618279"
> "0110467","autosomal recessive nonsyndromic deafness 12","omim","601386"
> "0080083","nonsyndromic congenital nail disorder 5","omim","164800"
13604c28041
< "0090123","aromatic L-amino acid decarboxylase deficiency","omim","608643"
---
> "14264","benign neonatal seizures","omim","269720"
13605a28043,28044
> "3764","Denys-Drash syndrome","omim","194080"
> "0060445","congenital stromal corneal dystrophy","omim","610048"
13609a28049
> "0080343","autosomal recessive pyridoxine-refractory sideroblastic anemia 3","omim","616860"
13612c28052
< "0110133","Bardet-Biedl syndrome 11","omim","615988"
---
> "0060406","chromosome 18p deletion syndrome","omim","146390"
13614c28054
< "0110127","Bardet-Biedl syndrome 5","omim","615983"
---
> "0080068","Charcot-Marie-Tooth disease type 6","omim","616505"
13616c28056
< "0110124","Bardet-Biedl syndrome 2","omim","615981"
---
> "0110029","alpha thalassemia-intellectual disability syndrome type 1","omim","141750"
13621a28062
> "0060436","chromosome 22q11.2 microduplication syndrome","omim","608363"
13623c28064
< "1612","breast cancer","omim","114480"
---
> "5453","pulmonary venoocclusive disease","omim","265450"
13624a28066
> "1148","polydactyly","omim","174700"
13626a28069
> "0050945","spastic ataxia 7","omim","108650"
13628c28071,28075
< "1933","Rubinstein-Taybi syndrome","omim","180849"
---
> "0090069","giant axonal neuropathy 2","omim","610100"
> "0060300","complement component 7 deficiency","omim","610102"
> "0060426","chromosome 19p13.13 deletion syndrome","omim","613638"
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","615802"
> "4051","alveolar rhabdomyosarcoma","omim","268220"
13630,13631c28077,28079
< "0110763","hereditary spastic paraplegia 10","omim","604187"
< "0070082","schizophrenia 6","omim","603013"
---
> "4997","Camurati-Engelmann disease","omim","131300"
> "2977","primary hyperoxaluria","omim","260000"
> "0110097","short-rib thoracic dysplasia 9 with or without polydactyly","omim","266920"
13638,13639c28086,28089
< "0110493","autosomal recessive nonsyndromic deafness 35","omim","608565"
< "0050425","restless legs syndrome","omim","102300"
---
> "13884","sick sinus syndrome","omim","608567"
> "0111365","benign familial hematuria","omim","141200"
> "2236","congenital afibrinogenemia","omim","202400"
> "4890","juvenile myoclonic epilepsy","omim","254770"
13642a28093
> "0080102","congenital fiber-type disproportion","omim","255310"
13644d28094
< "699","mitochondrial myopathy","omim","251900"
13647a28098
> "0111538","paramyotonia congenita of Von Eulenburg","omim","168300"
13656,13657c28107,28108
< "0060307","autosomal dominant non-syndromic intellectual disability","omim","156200"
< "0110718","Warburg micro syndrome 3","omim","614222"
---
> "8986","narcolepsy","omim","614223"
> "1924","hypogonadism","omim","312300"
13658a28110,28111
> "0060850","annular pancreas","omim","167750"
> "0060062","familial juvenile hyperuricemic nephropathy","omim","614227"
13659a28113
> "0080063","autosomal recessive spinocerebellar ataxia 11","omim","614229"
13660a28115
> "0050961","spinocerebellar ataxia type 11","omim","604432"
13661a28117
> "0080420","early infantile epileptic encephalopathy 62","omim","617938"
13662a28119
> "0111585","carnitine-acylcarnitine translocase deficiency","omim","212138"
13666c28123
< "0060228","intracranial berry aneurysm","omim","610213"
---
> "0080434","early infantile epileptic encephalopathy 61","omim","617933"
13668c28125
< "0110727","neuronal ceroid lipofuscinosis 13","omim","615362"
---
> "3052","Balkan nephropathy","omim","124100"
13672,13673c28129,28131
< "0110595","Stromme syndrome","omim","243605"
< "1067","open-angle glaucoma","omim","608695"
---
> "0050660","Beare-Stevenson cutis gyrata syndrome","omim","123790"
> "0111324","juvenile absence epilepsy 1","omim","607631"
> "0080037","Worth's syndrome","omim","607636"
13675c28133
< "1067","open-angle glaucoma","omim","608696"
---
> "0080240","X-linked mental retardation 106","omim","300997"
13676a28135
> "2224","essential thrombocythemia","omim","614521"
13677a28137
> "10122","hyperpigmentation of eyelid","omim","145100"
13678a28139,28140
> "0110270","cataract 17 multiple types","omim","611544"
> "0111381","IVIC syndrome","omim","147750"
13682c28144,28146
< "1338","congenital dyserythropoietic anemia","omim","615631"
---
> "0060467","humeroradial synostosis","omim","143050"
> "0050990","episodic ataxia type 2","omim","108500"
> "0080334","aortic valve disease 2","omim","614823"
13685,13686c28149,28152
< "10591","pre-eclampsia","omim","614592"
< "0060170","generalized epilepsy with febrile seizures plus","omim","609800"
---
> "0111022","cone-rod dystrophy 16","omim","614500"
> "0111293","generalized epilepsy with febrile seizures plus 4","omim","609800"
> "0080084","nonsyndromic congenital nail disorder 6","omim","107000"
> "0050886","Troyer syndrome","omim","275900"
13689a28156
> "0110925","familial hemophagocytic lymphohistiocytosis 5","omim","613101"
13692,13695c28159,28162
< "1067","open-angle glaucoma","omim","611274"
< "0060170","generalized epilepsy with febrile seizures plus","omim","611277"
< "0060601","alpha-2-plasmin inhibitor deficiency","omim","262850"
< "0070272","hereditary nonpolyposis colorectal cancer type 5","omim","614350"
---
> "0060828","X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome","omim","300886"
> "0080470","early infantile epileptic encephalopathy 36","omim","300884"
> "0080297","Coffin-Siris syndrome 6","omim","617808"
> "0080509","Cornelia de Lange syndrome 5","omim","300882"
13696a28164,28165
> "10825","essential hypertension","omim","610262"
> "0110335","osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures","omim","166230"
13698,13699c28167,28169
< "0110293","autosomal recessive limb-girdle muscular dystrophy type 2P","omim","613818"
< "0070179","spermatogenic failure 14","omim","615842"
---
> "0050432","Asperger syndrome","omim","609954"
> "1856","cherubism","omim","118400"
> "8616","Peyronie's disease","omim","171000"
13700a28171
> "0060270","pontocerebellar hypoplasia type 2D","omim","613811"
13703a28175
> "0111187","distal muscular dystrophy with anterior tibial onset","omim","606768"
13705,13706c28177,28180
< "0110626","primary ciliary dyskinesia 2","omim","606763"
< "0070217","familial hyperinsulinemic hypoglycemia 6","omim","606762"
---
> "0080543","hyperprolinemia type 2","omim","239510"
> "9253","gastrointestinal stromal tumor","omim","606764"
> "0110339","osteogenesis imperfecta type 3","omim","259420"
> "0060465","fibrochondrogenesis","omim","228520"
13707a28182
> "0111241","congenital muscular dystrophy-dystroglycanopathy type A5","omim","613153"
13708a28184
> "0070216","familial hyperinsulinemic hypoglycemia 3","omim","602485"
13710,13712c28186,28194
< "0060462","Desbuquois dysplasia","omim","615777"
< "0070219","familial hyperinsulinemic hypoglycemia 1","omim","256450"
< "0090136","complex cortical dysplasia with other brain malformations 6","omim","615771"
---
> "0060648","anterior segment dysgenesis","omim","107250"
> "0080089","tubular aggregate myopathy","omim","160565"
> "0111588","Greenberg dysplasia","omim","215140ORDO:1426"
> "0060363","glycerol kinase deficiency","omim","307030"
> "0050650","familial atrial fibrillation","omim","615770"
> "0060868","leukoencephalopathy with vanishing white matter","omim","603896"
> "0060446","X-linked endothelial corneal dystrophy","omim","300779"
> "0060450","Lisch epithelial corneal dystrophy","omim","300778"
> "10609","rickets","omim","277440"
13713a28196
> "0070148","hereditary sensory neuropathy type 1B","omim","608088"
13715a28199,28200
> "0050793","short QT syndrome","omim","609622"
> "0111425","restrictive cardiomyopathy 1","omim","115210"
13716a28202
> "0111524","autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5","omim","618098"
13719a28206
> "0080328","Culler-Jones syndrome","omim","615849"
13721c28208
< "0110209","Charcot-Marie-Tooth disease X-linked dominant 1","omim","302800"
---
> "0080377","peroxisomal biogenesis disorder","omim","214100"
13723c28210
< "0110925","familial hemophagocytic lymphohistiocytosis 5","omim","613101"
---
> "0060754","familial temporal lobe epilepsy 8","omim","616461"
13726c28213,28214
< "0050568","spondylocostal dysostosis","omim","122600"
---
> "0110935","nemaline myopathy 6","omim","609273"
> "9822","partial central choroid dystrophy","omim","613105"
13727a28216
> "13941","benign paroxysmal positional nystagmus","omim","613106"
13730c28219,28220
< "0050444","infantile Refsum disease","omim","266510"
---
> "10582","Refsum disease","omim","266510"
> "0070230","benign recurrent intrahepatic cholestasis","omim","243300"
13732c28222,28223
< "0110102","atopic dermatitis 6","omim","605845"
---
> "0060415","chromosome 2p16.1-p15 deletion syndrome","omim","612513"
> "0060244","specific language impairment","omim","612514"
13734,13736c28225,28229
< "0080315","megalencephalic leukoencephalopathy with subcortical cysts","omim","604004"
< "0080361","trimethylaminuria","omim","602079"
< "12804","mucopolysaccharidosis IV","omim","253000"
---
> "9521","Laron syndrome","omim","262500"
> "3301","gonadoblastoma","omim","424500"
> "0111356","hydrolethalus syndrome 2","omim","614120"
> "0110623","primary ciliary dyskinesia 15","omim","613808"
> "0080076","Neu-Laxova syndrome 1","omim","256520"
13738c28231,28233
< "0070260","congenital disorder of glycosylation type IIh","omim","611182"
---
> "0110032","autosomal dominant Alport syndrome","omim","104200"
> "11512","Budd-Chiari syndrome","omim","600880"
> "417","autoimmune hypersensitivity disease","omim","109100"
13740,13741c28235,28237
< "0060296","congenital secretory chloride diarrhea 1","omim","214700"
< "0070264","congenital disorder of glycosylation type IIl","omim","614576"
---
> "2058","chronic mucocutaneous candidiasis","omim","613956"
> "1924","hypogonadism","omim","241100"
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","611096"
13746c28242
< "0110231","cataract 1 multiple types","omim","116200"
---
> "0090068","giant axonal neuropathy 1","omim","256850"
13748a28245,28246
> "1761","Melkersson-Rosenthal syndrome","omim","155900"
> "9487","Meckel's diverticulum","omim","155140"
13749a28248
> "0111232","congenital muscular dystrophy-dystroglycanopathy type A9","omim","616538"
13750a28250,28251
> "0080417","early infantile epileptic encephalopathy 38","omim","617020"
> "12177","common variable immunodeficiency","omim","240500"
13752c28253,28254
< "0110866","congenital stationary night blindness 1H","omim","617024"
---
> "7148","rheumatoid arthritis","omim","180300"
> "987","alopecia","omim","203655"
13762c28264
< "0110549","autosomal dominant nonsyndromic deafness 18","omim","606012"
---
> "0080019","metaphyseal dysplasia","omim","215050"
13764d28265
< "0060174","GABA aminotransferase deficiency","omim","613163"
13766c28267
< "0070248","autosomal recessive Emery-Dreifuss muscular dystrophy 3","omim","616516"
---
> "0060464","Feingold syndrome","omim","164280"
13771,13774c28272,28280
< "1339","Diamond-Blackfan anemia","omim","615550"
< "9255","frontotemporal dementia","omim","600795"
< "0111062","familial hypobetalipoproteinemia 1","omim","615558"
< "0110119","autoimmune lymphoproliferative syndrome type 3","omim","615559"
---
> "0111204","distal hereditary motor neuronopathy type 5A","omim","600794"
> "0060293","autosomal dominant chondrodysplasia punctata","omim","118651"
> "0060293","autosomal dominant chondrodysplasia punctata","omim","118650"
> "1933","Rubinstein-Taybi syndrome","omim","180849"
> "0110962","brachydactyly-preaxial hallux varus syndrome","omim","112450"
> "1392","pseudopapilledema","omim","177800"
> "0050650","familial atrial fibrillation","omim","612201"
> "0060902","Norman-Roberts syndrome","omim","257320"
> "0111510","Marshall syndrome","omim","154780"
13776d28281
< "0111108","maturity-onset diabetes of the young type 10","omim","613370"
13777a28283
> "0111500","combined oxidative phosphorylation deficiency 23","omim","616198"
13786a28293,28294
> "2734","keratosis follicularis","omim","124200"
> "10300","Raynaud disease","omim","179600"
13788c28296,28298
< "0050715","methylmalonic aciduria and homocystinuria type cblC","omim","277400"
---
> "0110577","autosomal dominant nonsyndromic deafness 51","omim","613558"
> "0050773","paraganglioma","omim","168000"
> "0111193","facioscapulohumeral muscular dystrophy 2","omim","158901"
13790,13791c28300,28306
< "0080139","multiple congenital anomalies-hypotonia-seizures syndrome 2","omim","300868"
< "0110933","nemaline myopathy 11","omim","617336"
---
> "2187","amelogenesis imperfecta","omim","104500"
> "0080433","early infantile epileptic encephalopathy 51","omim","617339"
> "0050644","arterial calcification of infancy","omim","208000"
> "0110320","hypertrophic cardiomyopathy 14","omim","613251"
> "0080170","normophosphatemic familial tumoral calcinosis","omim","610455"
> "0111268","autosomal recessive hyaline body myopathy","omim","255160"
> "0060575","3MC syndrome 1","omim","257920"
13793a28309
> "4447","cystoid macular edema","omim","153880"
13796c28312
< "0050881","inclusion body myopathy with Paget disease of bone and frontotemporal dementia","omim","615422"
---
> "0111384","inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2","omim","615422"
13798c28314
< "0050881","inclusion body myopathy with Paget disease of bone and frontotemporal dementia","omim","615424"
---
> "13533","osteopetrosis","omim","259700"
13800a28317
> "11193","syndactyly","omim","186200"
13805a28323
> "9649","congenital nystagmus","omim","614826"
13807,13808c28325,28326
< "0060170","generalized epilepsy with febrile seizures plus","omim","612279"
< "0070216","familial hyperinsulinemic hypoglycemia 3","omim","602485"
---
> "0070236","Loeys-Dietz syndrome 5","omim","615582"
> "0070167","spermatogenic failure 6","omim","102530"
13809a28328,28333
> "14330","Parkinson's disease","omim","168600"
> "0080554","congenital disorder of glycosylation Ib","omim","602579"
> "12098","trigeminal neuralgia","omim","190400"
> "9263","homocystinuria","omim","236250"
> "0111342","dermatopathia pigmentosa reticularis","omim","125595"
> "0060812","syndromic X-linked intellectual disability Siderius type","omim","300263"
13810a28335
> "0060804","syndromic X-linked intellectual disability 12","omim","309545"
13813c28338,28339
< "0110755","type 1 diabetes mellitus 18","omim","605598"
---
> "0080428","early infantile epileptic encephalopathy 45","omim","617153"
> "0080337","mitochondrial DNA depletion syndrome 15","omim","617156"
13815c28341,28343
< "0110320","hypertrophic cardiomyopathy 14","omim","613251"
---
> "0080325","tuberous sclerosis 2","omim","613254"
> "0050649","atransferrinemia","omim","209300"
> "0080169","tricuspid atresia","omim","605067"
13817,13819c28345,28348
< "11193","syndactyly","omim","186200"
< "0070167","spermatogenic failure 6","omim","102530"
< "9263","homocystinuria","omim","236250"
---
> "0090066","Fanconi-like syndrome","omim","227850"
> "0060253","scapuloperoneal myopathy","omim","300695"
> "4751","striatonigral degeneration","omim","271930"
> "0111416","trichohepatoenteric syndrome 2","omim","614602"
13822a28352,28354
> "0060649","congenital hereditary endothelial dystrophy of cornea","omim","217700"
> "14744","Partington syndrome","omim","309510"
> "13832","patent ductus arteriosus","omim","607411"
13825,13826c28357,28360
< "14793","hypohidrotic ectodermal dysplasia","omim","305100"
< "0050800","creatine transporter deficiency","omim","300352"
---
> "0111457","STING-associated vasculopathy with onset in infancy","omim","615934"
> "0111372","autosomal dominant endosteal hyperostosis","omim","144750"
> "13543","hyperparathyroidism","omim","610071"
> "3783","Coffin-Lowry syndrome","omim","303600"
13828c28362,28364
< "2224","essential thrombocythemia","omim","187950"
---
> "0110033","autosomal recessive Alport syndrome","omim","203780"
> "0060577","3MC syndrome 3","omim","248340"
> "0110924","familial hemophagocytic lymphohistiocytosis 4","omim","603552"
13833c28369
< "0110196","Charcot-Marie-Tooth disease type 4G","omim","605285"
---
> "0060799","syndromic X-linked intellectual disability Lubs type","omim","300260"
13835c28371
< "0060474","familial erythrocytosis 2","omim","263400"
---
> "0050775","schneckenbecken dysplasia","omim","269250"
13836a28373
> "0111494","combined oxidative phosphorylation deficiency 4","omim","610678"
13838c28375,28376
< "0110475","autosomal recessive nonsyndromic deafness 1A","omim","220290"
---
> "0050636","familial visceral amyloidosis","omim","105200"
> "0090064","familial cold autoinflammatory syndrome 3","omim","614468"
13840c28378
< "12118","pulmonary hemosiderosis","omim","235500"
---
> "0050453","lissencephaly","omim","300067"
13841a28380
> "0080220","major affective disorder 1","omim","125480"
13843a28383
> "0111446","progressive myoclonus epilepsy 3","omim","611726"
13846c28386,28387
< "0110731","neuronal ceroid lipofuscinosis 3","omim","204200"
---
> "0111269","autosomal dominant hyaline body myopathy","omim","608358"
> "0110102","atopic dermatitis 6","omim","605845"
13849c28390
< "0070123","congenital nongoitrous hypothyroidism 4","omim","275100"
---
> "3948","adrenocortical carcinoma","omim","202300"
13851c28392,28393
< "0111035","CADASIL 1","omim","125310"
---
> "0110435","dilated cardiomyopathy 1GG","omim","613642"
> "0110079","Leber congenital amaurosis 8","omim","613835"
13856c28398,28399
< "14717","centronuclear myopathy","omim","615959"
---
> "0050985","spinocerebellar ataxia type 38","omim","615957"
> "4603","epidermolytic hyperkeratosis","omim","113800"
13861a28405
> "12241","beta thalassemia","omim","187550"
13862a28407,28408
> "0060547","Hermansky-Pudlak syndrome 9","omim","614171"
> "14775","brittle cornea syndrome","omim","614170"
13864a28411
> "5363","myxoid liposarcoma","omim","613488"
13865a28413,28415
> "0080089","tubular aggregate myopathy","omim","615883"
> "0080338","familial erythrocytosis 3","omim","609820"
> "14669","acrodysostosis","omim","614613"
13867c28417
< "0110063","amelogenesis imperfecta hypomaturation type 2A5","omim","615887"
---
> "0060673","Peters anomaly","omim","604229"
13868a28419
> "0080100","congenital myopathy","omim","255300"
13870,13871c28421,28426
< "0110984","Joubert syndrome 15","omim","614464"
< "0110986","Joubert syndrome 17","omim","614615"
---
> "0050458","juvenile myelomonocytic leukemia","omim","607785"
> "0111055","platelet-type bleeding disorder 20","omim","616913"
> "2748","glycogen storage disease III","omim","232400"
> "3534","Lafora disease","omim","254780"
> "0060365","mandibulofacial dysostosis with alopecia","omim","616367"
> "0111271","Oliver-McFarlane syndrome","omim","275400"
13875,13876c28430,28431
< "0110851","rhizomelic chondrodysplasia punctata type 1","omim","215100"
< "0060170","generalized epilepsy with febrile seizures plus","omim","604403"
---
> "2962","Cockayne syndrome","omim","133540"
> "0111294","generalized epilepsy with febrile seizures plus 2","omim","604403"
13877a28433,28436
> "3805","porokeratosis","omim","175800"
> "0080594","hyper IgE recurrent infection syndrome 2","omim","243700"
> "0060572","Ritscher-Schinzel syndrome 2","omim","300963"
> "0080289","orofaciodigital syndrome XVII","omim","617926"
13879c28438,28441
< "0110256","cataract 21 multiple types","omim","610202"
---
> "0060274","pontocerebellar hypoplasia type 5","omim","610204"
> "0060227","Adams-Oliver syndrome","omim","614219"
> "4989","pancreatitis","omim","167800"
> "0090032","Silverman-Handmaker type dyssegmental dysplasia","omim","224410"
13882c28444
< "0110567","autosomal dominant nonsyndromic deafness 41","omim","608224"
---
> "1324","lung cancer","omim","614210"
13884,13885c28446,28448
< "0050592","asphyxiating thoracic dystrophy","omim","208500"
< "0110284","autosomal recessive limb-girdle muscular dystrophy type 2L","omim","611307"
---
> "0080432","early infantile epileptic encephalopathy 60","omim","617929"
> "0070147","hereditary sensory neuropathy type 2C","omim","614213"
> "0060285","parietal foramina","omim","609597"
13887c28450
< "0060737","junctional epidermolysis bullosa Herlitz type","omim","226700"
---
> "0050941","spastic ataxia 2","omim","611302"
13889a28453
> "0060282","persistent hyperplastic primary vitreous","omim","611308"
13890a28455,28457
> "2229","factor XI deficiency","omim","612416"
> "0060301","type I complement component 8 deficiency","omim","613790"
> "0060417","3p- syndrome","omim","613792"
13892,13893c28459,28465
< "0070237","Loeys-Dietz syndrome 3","omim","613795"
< "0060536","mitochondrial complex I deficiency","omim","252010"
---
> "0060833","Griscelli syndrome type 2","omim","607624"
> "0111552","scapuloperoneal spinal muscular atrophy","omim","181405"
> "0111312","idiopathic generalized epilepsy 11","omim","607628"
> "0111581","C syndrome","omim","211750"
> "0080209","sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay","omim","616084"
> "14793","hypohidrotic ectodermal dysplasia","omim","305100"
> "9631","Pelger-Huet anomaly","omim","169400"
13894a28467,28469
> "8534","gastroesophageal reflux disease","omim","109350"
> "0111534","multicentric carpotarsal osteolysis syndrome","omim","166300"
> "0110346","osteogenesis imperfecta type 10","omim","613848"
13896c28471,28473
< "0110241","cataract 41","omim","116400"
---
> "1024","leprosy","omim","607572"
> "2373","hereditary elliptocytosis","omim","611804"
> "0111346","epidermolysis bullosa simplex with mottled pigmentation","omim","131960"
13901,13902c28478,28481
< "0111154","postural orthostatic tachycardia syndrome","omim","604715"
< "0110557","autosomal dominant nonsyndromic deafness 28","omim","608641"
---
> "0090123","aromatic L-amino acid decarboxylase deficiency","omim","608643"
> "0050489","multinodular goiter","omim","138800"
> "0110550","autosomal dominant nonsyndromic deafness 20","omim","604717"
> "0080058","autosomal recessive spinocerebellar ataxia 14","omim","615386"
13903a28483
> "2224","essential thrombocythemia","omim","187950"
13904a28485
> "0111317","idiopathic generalized epilepsy 2","omim","606972"
13906a28488
> "0060247","Smith-McCort dysplasia","omim","615222"
13908d28489
< "0050425","restless legs syndrome","omim","611242"
13911,13912c28492,28494
< "0060233","cardiofaciocutaneous syndrome","omim","115150"
< "0110528","autosomal recessive nonsyndromic deafness 83","omim","613685"
---
> "0111460","cardiofaciocutaneous syndrome 1","omim","115150"
> "0080309","fatal infantile hypertonic myofibrillar myopathy","omim","613869"
> "0080490","mucolipidosis type IV","omim","252650"
13915c28497
< "0060170","generalized epilepsy with febrile seizures plus","omim","613863"
---
> "9884","muscular dystrophy","omim","600416"
13917c28499
< "0070121","Meckel syndrome 7","omim","267010"
---
> "0050565","autosomal recessive nonsyndromic deafness","omim","607197"
13920c28502,28506
< "0070058","Helsmoortel-Van Der Aa Syndrome","omim","615873"
---
> "11599","Frey syndrome","omim","144100"
> "0111360","hypotrichosis-lymphedema-telangiectasia-renal defect syndrome","omim","137940"
> "0060244","specific language impairment","omim","606712"
> "0060239","Van der Woude syndrome","omim","606713"
> "0060244","specific language impairment","omim","606711"
13924c28510,28511
< "0090135","complex cortical dysplasia with other brain malformations 5","omim","615763"
---
> "6682","spondylolisthesis","omim","184200"
> "0060735","epidermolysis bullosa simplex Dowling-Meara type","omim","131760"
13934c28521
< "14448","46 XY gonadal dysgenesis","omim","616067"
---
> "0080114","mitochondrial complex III deficiency nuclear type 5","omim","615160"
13937,13938c28524,28527
< "0070194","autosomal recessive chronic granulomatous disease cytochrome b-positive type III","omim","613960"
< "0110440","dilated cardiomyopathy 1J","omim","605362"
---
> "0110196","Charcot-Marie-Tooth disease type 4G","omim","605285"
> "0080115","mitochondrial complex III deficiency nuclear type 6","omim","615453"
> "14448","46 XY gonadal dysgenesis","omim","400044"
> "0090027","split hand-foot malformation 2","omim","313350"
13939a28529
> "3911","progeria","omim","176670"
13942a28533
> "10582","Refsum disease","omim","266500"
13944c28535
< "0110670","congenital myasthenic syndrome 9","omim","616325"
---
> "0080419","early infantile epileptic encephalopathy 50","omim","616457"
13946c28537
< "0110819","hereditary spastic paraplegia 74","omim","616451"
---
> "0110574","autosomal dominant nonsyndromic deafness 4B","omim","614614"
13948c28539,28540
< "0110004","3-methylglutaconic aciduria type 3","omim","258501"
---
> "0111435","optic atrophy 6","omim","258500"
> "0060739","hand-foot-genital syndrome","omim","140000"
13950c28542,28543
< "1339","Diamond-Blackfan anemia","omim","612528"
---
> "13241","Behcet's disease","omim","109650"
> "0111103","maturity-onset diabetes of the young type 4","omim","606392"
13952,13953c28545,28546
< "12804","mucopolysaccharidosis IV","omim","253010"
< "12638","hypertrophic pyloric stenosis","omim","612525"
---
> "0050524","maturity-onset diabetes of the young","omim","606391"
> "0090115","spinocerebellar ataxia type 1 with axonal neuropathy","omim","607250"
13955c28548
< "1339","Diamond-Blackfan anemia","omim","612527"
---
> "0060013","X-linked severe combined immunodeficiency","omim","300400"
13959,13960c28552,28555
< "0050636","familial visceral amyloidosis","omim","105200"
< "0050776","non-syndromic X-linked intellectual disability","omim","300387"
---
> "0080086","nonsyndromic congenital nail disorder 8","omim","607523"
> "0111551","neurogenic scapuloperoneal syndrome Kaeser type","omim","181400"
> "0110214","cleft soft palate","omim","119570"
> "0060824","syndromic X-linked intellectual disability Raymond type","omim","300799"
13962c28557,28560
< "4990","essential tremor","omim","614782"
---
> "0111281","psoriasis 15","omim","616106"
> "0111431","essential tremor 4","omim","614782"
> "0060401","chromosome 16q22 deletion syndrome","omim","614541"
> "0080452","early infantile epileptic encephalopathy 28","omim","616211"
13963a28562,28563
> "1391","Norum disease","omim","245900"
> "3928","adiposis dolorosa","omim","103200"
13966,13967c28566,28572
< "1270","hereditary hemorrhagic telangiectasia","omim","187300"
< "0050566","X-linked nonsyndromic deafness","omim","304500"
---
> "12118","pulmonary hemosiderosis","omim","235500"
> "0060459","chromosome 3q29 microduplication syndrome","omim","611936"
> "0111320","idiopathic generalized epilepsy 5","omim","611934"
> "12120","pulmonary alveolar proteinosis","omim","610921"
> "10003","sensorineural hearing loss","omim","304400"
> "0050590","severe congenital neutropenia","omim","202700"
> "0080131","mitochondrial DNA depletion syndrome 13","omim","615471"
13969c28574,28577
< "12236","primary biliary cirrhosis","omim","613008"
---
> "11164","band keratopathy","omim","217500"
> "5723","optic atrophy","omim","165500"
> "11830","myopia","omim","609995"
> "0080075","Neu-Laxova syndrome 2","omim","616038"
13972,13973c28580,28582
< "0050428","nonepidermolytic palmoplantar keratoderma","omim","613000"
< "0070069","autosomal dominant non-syndromic intellectual disability 39","omim","616521"
---
> "0111133","focal segmental glomerulosclerosis 8","omim","616032"
> "9675","pulmonary emphysema","omim","130700"
> "0090081","hypogonadotropic hypogonadism 22 with or without anosmia","omim","616030"
13978c28587
< "0060902","Norman-Roberts syndrome","omim","257320"
---
> "0110702","hypotrichosis 5","omim","612841"
13981c28590,28591
< "0060238","Van Maldergem syndrome","omim","615546"
---
> "0080586","Van Maldergem syndrome 2","omim","615546"
> "0110667","congenital myasthenic syndrome 5","omim","603034"
13986c28596
< "0090006","renal coloboma syndrome","omim","120330"
---
> "0050591","tooth agenesis","omim","602639"
13987a28598
> "0110069","FTDALS4","omim","616439"
13989,13990c28600,28601
< "0050431","arrhythmogenic right ventricular cardiomyopathy","omim","107970"
< "0080119","mitochondrial DNA depletion syndrome 1","omim","603041"
---
> "0080080","nonsyndromic congenital nail disorder 2","omim","149300"
> "0110912","leukocyte adhesion deficiency 3","omim","612840"
13994c28605
< "0050877","pancreatic agenesis","omim","260370"
---
> "0110934","nemaline myopathy 7","omim","610687"
13996,13997c28607,28611
< "0050535","exudative vitreoretinopathy","omim","613310"
< "0060791","hypomyelinating leukodystrophy 9","omim","616140"
---
> "0111258","pentosuria","omim","260800"
> "0060467","humeroradial synostosis","omim","236400"
> "0111408","exudative vitreoretinopathy 5","omim","613310"
> "0060386","Chilblain lupus","omim","610448"
> "14116","multiple symmetric lipomatosis","omim","151900"
14003a28618,28620
> "0080576","spondyloepimetaphyseal dysplasia, Genevieve-type","omim","610442"
> "0111054","von Willebrand's disease 3","omim","277480"
> "0111536","Buschke-Ollendorff syndrome","omim","166700"
14004a28622,28623
> "0110018","age related macular degeneration 6","omim","613757"
> "0060640","ethylmalonic encephalopathy","omim","602473"
14006c28625,28627
< "0050449","pachyonychia congenita","omim","167210"
---
> "437","myasthenia gravis","omim","254200"
> "0111310","familial febrile seizures 2","omim","602477"
> "0050580","hereditary lymphedema","omim","153100"
14007a28629,28631
> "14283","primary hypertrophic osteoarthropathy","omim","259100"
> "0111455","GRACILE syndrome","omim","603358"
> "0080255","Meier-Gorlin syndrome 8","omim","617564"
14010a28635
> "0080254","orofaciodigital syndrome XVI","omim","617563"
14012c28637,28638
< "0110469","autosomal recessive nonsyndromic deafness 14","omim","603678"
---
> "0060418","chromosome 3q13.31 deletion syndrome","omim","615433"
> "0060244","specific language impairment","omim","615432"
14015c28641,28644
< "1056","oculocerebrorenal syndrome","omim","309000"
---
> "0110672","congenital myasthenic syndrome 21","omim","617239"
> "0060293","autosomal dominant chondrodysplasia punctata","omim","602497"
> "0110220","Brugada syndrome 3","omim","611875"
> "0110559","autosomal dominant nonsyndromic deafness 2B","omim","612644"
14017c28646,28649
< "3948","adrenocortical carcinoma","omim","202300"
---
> "8986","narcolepsy","omim","612851"
> "0110471","autosomal recessive nonsyndromic deafness 16","omim","603720"
> "0080132","Sengers syndrome","omim","212350"
> "0080222","pseudohypoparathyroidism type IB","omim","603233"
14019c28651,28654
< "0110435","dilated cardiomyopathy 1GG","omim","613642"
---
> "0070237","Loeys-Dietz syndrome 3","omim","613795"
> "14080","glucocorticoid-remediable aldosteronism","omim","103900"
> "0110376","retinitis pigmentosa 41","omim","612095"
> "0111035","CADASIL 1","omim","125310"
14021c28656
< "0110254","cataract 25","omim","605728"
---
> "0110955","Waardenburg syndrome type 4C","omim","613266"
14023c28658
< "0111065","autosomal recessive distal spinal muscular atrophy 2","omim","605726"
---
> "0111065","distal spinal muscular atrophy 2","omim","605726"
14026c28661,28662
< "3393","coronary artery disease","omim","611139"
---
> "0110583","autosomal dominant nonsyndromic deafness 59","omim","612642"
> "0111334","congenital leptin deficiency","omim","614962"
14027a28664,28667
> "0080050","acromesomelic dysplasia, Maroteaux type","omim","602875"
> "0060277","pontocerebellar hypoplasia type 8","omim","614961"
> "0080498","ovarian dysgenesis 6","omim","618078"
> "0080566","congenital disorder of glycosylation In","omim","612015"
14031,14032c28671,28672
< "0060822","syndromic X-linked intellectual disability Cabezas type","omim","300354"
< "0060883","intestinal hypomagnesemia 1","omim","602014"
---
> "0060276","pontocerebellar hypoplasia type 7","omim","614969"
> "0050800","creatine transporter deficiency","omim","300352"
14033a28674,28675
> "0110419","retinitis pigmentosa with or without situs inversus","omim","615434"
> "0080596","hyper IgE recurrent infection syndrome 4","omim","618523"
14037,14038c28679,28680
< "0110280","autosomal recessive limb-girdle muscular dystrophy type 2F","omim","601287"
< "0060896","autosomal recessive early-onset Parkinson's disease 23","omim","616840"
---
> "9074","systemic lupus erythematosus","omim","610065"
> "0060896","Parkinson's disease 23","omim","616840"
14039a28682
> "4022","ureterocele","omim","191650"
14042a28686
> "1930","Laurence-Moon syndrome","omim","245800"
14044c28688,28692
< "10584","retinitis pigmentosa","omim","268000"
---
> "0080556","congenital disorder of glycosylation Id","omim","601110"
> "0060612","abdominal obesity-metabolic syndrome 3","omim","615812"
> "0080275","Joubert syndrome 30","omim","617622"
> "4154","dentinogenesis imperfecta","omim","125490"
> "10629","microphthalmia","omim","206900"
14048c28696,28698
< "0110115","autoimmune lymphoproliferative syndrome type 2A","omim","603909"
---
> "14775","brittle cornea syndrome","omim","229200"
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","615817"
> "0080130","mitochondrial DNA depletion syndrome 12a","omim","617184"
14051c28701,28702
< "0110779","hereditary spastic paraplegia 28","omim","609340"
---
> "6420","pulmonary valve stenosis","omim","265500"
> "0060576","3MC syndrome 2","omim","265050"
14054c28705,28706
< "0080523","adult-onset leukoencephalopathy with axonal spheroids and pigmented glia","omim","221820"
---
> "0111228","Sveinsson chorioretinal atrophy","omim","108985"
> "1928","Williams-Beuren syndrome","omim","194050"
14056c28708
< "0070119","Meckel syndrome 5","omim","611561"
---
> "0080574","congenital disorder of glycosylation Iy","omim","300934"
14058c28710
< "0110201","Charcot-Marie-Tooth disease recessive intermediate A","omim","608340"
---
> "0050650","familial atrial fibrillation","omim","607554"
14060a28713,28716
> "9649","congenital nystagmus","omim","608345"
> "10865","abducens nerve disease","omim","100200"
> "0060542","Hermansky-Pudlak syndrome 4","omim","614073"
> "0111352","D-2-hydroxyglutaric aciduria 2","omim","613657"
14062a28719
> "0050984","spinocerebellar ataxia type 37","omim","615945"
14064c28721,28723
< "12177","common variable immunodeficiency","omim","613493"
---
> "0060544","Hermansky-Pudlak syndrome 6","omim","614075"
> "0110443","dilated cardiomyopathy 1B","omim","600884"
> "0111256","hyperferritinemia-cataract syndrome","omim","600886"
14067c28726
< "0110258","cataract 10 multiple types","omim","600881"
---
> "0060545","Hermansky-Pudlak syndrome 7","omim","614076"
14069c28728,28729
< "12177","common variable immunodeficiency","omim","613494"
---
> "0070183","spermatogenic failure 5","omim","243060"
> "0080108","myoglobinuria","omim","268200"
14071,14074c28731,28738
< "0060895","autosomal dominant Parkinson's disease 4","omim","605543"
< "0110710","hypotrichosis 13","omim","615896"
< "0060170","generalized epilepsy with febrile seizures plus","omim","604233"
< "0110331","Leber congenital amaurosis 3","omim","604232"
---
> "0080407","orofacial cleft 14","omim","615892"
> "0060895","Parkinson's disease 4","omim","605543"
> "6245","renal oncocytoma","omim","553000"
> "0111302","generalized epilepsy with febrile seizures plus 1","omim","604233"
> "9248","Pallister-Hall syndrome","omim","146510"
> "0110473","autosomal recessive nonsyndromic deafness 18A","omim","602092"
> "14762","calcaneonavicular coalition","omim","186400"
> "0111336","craniofacial-deafness-hand syndrome","omim","122880"
14077c28741,28742
< "0060464","Feingold syndrome","omim","164280"
---
> "0060540","Hermansky-Pudlak syndrome 2","omim","608233"
> "0060668","anencephaly","omim","206500"
14082c28747,28748
< "0111074","progressive familial heart block type IA","omim","113900"
---
> "1040","chronic lymphocytic leukemia","omim","609630"
> "0111482","combined oxidative phosphorylation deficiency 36","omim","617950"
14084c28750,28751
< "0110043","Alzheimer's disease 10","omim","609636"
---
> "0080110","multiple pterygium syndrome","omim","312150"
> "0070332","multiple mitochondrial dysfunctions syndrome 6","omim","617954"
14086a28754
> "0050889","non-syndromic intellectual disability","omim","614202"
14088a28757
> "0110575","autosomal dominant nonsyndromic deafness 5","omim","600994"
14091,14092c28760,28761
< "0080379","nephrotic syndrome type 2","omim","600995"
< "10871","age related macular degeneration","omim","603075"
---
> "9074","systemic lupus erythematosus","omim","605480"
> "0111101","maturity-onset diabetes of the young type 5","omim","137920"
14094a28764
> "0050857","Perrault syndrome","omim","615300"
14096c28766
< "0060761","familial chronic myelocytic leukemia-like syndrome","omim","600080"
---
> "0050592","asphyxiating thoracic dystrophy","omim","208500"
14098c28768
< "14717","centronuclear myopathy","omim","255200"
---
> "2908","Treacher Collins syndrome","omim","248390"
14099a28770,28772
> "2750","glycogen storage disease IV","omim","232500"
> "0111387","familial isolated hypoparathyroidism","omim","146200"
> "0060302","type II complement component 8 deficiency","omim","613789"
14101,14102c28774,28778
< "0110024","age related macular degeneration 12","omim","613784"
< "0050454","periventricular nodular heterotopia","omim","612881"
---
> "11722","myotonic dystrophy type 1","omim","160900"
> "0070112","Niemann-Pick disease type B","omim","607616"
> "0050797","peroxisomal acyl-CoA oxidase deficiency","omim","264470"
> "0111589","COACH syndrome","omim","216360"
> "0110063","amelogenesis imperfecta hypomaturation type 2A5","omim","615887"
14105,14107c28781,28784
< "0080519","PAPA syndrome","omim","604416"
< "0111121","nephronophthisis 13","omim","614377"
< "0110089","asphyxiating thoracic dystrophy 5","omim","614376"
---
> "1338","congenital dyserythropoietic anemia","omim","224120"
> "12798","mucopolysaccharidosis","omim","607014"
> "0050811","congenital adrenal hyperplasia","omim","202110"
> "2861","congenital nonspherocytic hemolytic anemia","omim","206300"
14117a28795,28796
> "0060298","complement component 4b deficiency","omim","614379"
> "0080033","craniometaphyseal dysplasia","omim","614378"
14119c28798,28800
< "0050770","polycystic liver disease","omim","174050"
---
> "0050642","hypochromic microcytic anemia","omim","615234"
> "3083","chronic obstructive pulmonary disease","omim","606963"
> "1148","polydactyly","omim","174500"
14123c28804
< "0070093","schizophrenia 18","omim","615232"
---
> "0111115","nephronophthisis 4","omim","606966"
14125a28807,28808
> "0111377","fetal akinesia deformation sequence syndrome 1","omim","208150"
> "0050694","Brown-Vialetto-Van Laere syndrome","omim","211530"
14126a28810,28811
> "14219","renal tubular acidosis","omim","179830"
> "0080221","major affective disorder 2","omim","309200"
14129,14130c28814,28815
< "0110324","hypertrophic cardiomyopathy 18","omim","613874"
< "0070205","familial partial lipodystrophy type 4","omim","613877"
---
> "3687","MELAS syndrome","omim","540000"
> "0060642","recessive dystrophic epidermolysis bullosa","omim","226600"
14131a28817
> "0111424","branchiootorenal syndrome 2","omim","610896"
14133c28819,28820
< "0050651","atrioventricular septal defect","omim","614474"
---
> "0110896","inflammatory bowel disease 16","omim","612259"
> "0070018","autosomal dominant dyskeratosis congenita 3","omim","613990"
14135a28823
> "0110809","hereditary spastic paraplegia 57","omim","615658"
14138,14139c28826,28828
< "13270","erythropoietic protoporphyria","omim","300752"
< "0110355","retinitis pigmentosa 32","omim","609913"
---
> "13401","angioid streaks","omim","607140"
> "0070078","schizophrenia 2","omim","603342"
> "0060063","sideroblastic anemia 1","omim","300751"
14143,14145c28832,28835
< "14179","Bruton-type agammaglobulinemia","omim","300755"
< "0060638","neonatal diabetes mellitus with congenital hypothyroidism","omim","610199"
< "0080405","orofacial cleft 12","omim","612858"
---
> "14179","X-linked agammaglobulinemia","omim","300755"
> "10825","essential hypertension","omim","607329"
> "0060262","gallbladder disease","omim","609919"
> "0060262","gallbladder disease","omim","609918"
14148a28839
> "0050994","episodic ataxia type 6","omim","612656"
14153c28844,28847
< "0050591","tooth agenesis","omim","602639"
---
> "0060641","endocrine-cerebro-osteodysplasia syndrome","omim","612651"
> "0111426","restrictive cardiomyopathy 2","omim","609578"
> "0080241","syndromic X-linked mental retardation 35","omim","300998"
> "0111519","autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions  6","omim","615156"
14154a28849,28850
> "10488","imperforate anus","omim","301800"
> "0110648","long QT syndrome 6","omim","613693"
14157,14160c28853,28857
< "0080457","microcephaly, seizures, and developmental delay","omim","613402"
< "0110646","long QT syndrome 3","omim","603830"
< "0060287","cornea plana","omim","121400"
< "0090100","ocular albinism with sensorineural deafness","omim","103470"
---
> "0060444","granular corneal dystrophy 2","omim","607541"
> "0060229","Baraitser-Winter syndrome","omim","243310"
> "0050675","Birk-Barel syndrome","omim","612292"
> "0110914","infantile hypophosphatasia","omim","241500"
> "0060867","macrocephaly-autism syndrome","omim","605309"
14161a28859,28860
> "14448","46 XY gonadal dysgenesis","omim","614279"
> "0111192","facioscapulohumeral muscular dystrophy 1","omim","158900"
14164c28863
< "0110225","Brugada syndrome 8","omim","613123"
---
> "0080107","microcephaly and chorioretinopathy 3","omim","616335"
14166c28865,28866
< "0110224","Brugada syndrome 7","omim","613120"
---
> "1485","cystic fibrosis","omim","219700"
> "8893","psoriasis","omim","177900"
14169a28870
> "2538","Landau-Kleffner syndrome","omim","245570"
14175c28876
< "0110067","juvenile amyotrophic lateral sclerosis with dementia","omim","205200"
---
> "628","combined T cell and B cell immunodeficiency","omim","312863"
14177c28878,28883
< "11722","myotonic dystrophy type 1","omim","160900"
---
> "0060412","chromosome 1q41-q42 deletion syndrome","omim","612530"
> "0111562","overhydrated hereditary stomatocytosis","omim","185000"
> "0060671","cerebral cavernous malformation 3","omim","603285"
> "0060670","cerebral cavernous malformation 2","omim","603284"
> "13543","hyperparathyroidism","omim","145001"
> "0110238","cataract 18","omim","610019"
14181a28888,28889
> "0050960","spinocerebellar ataxia type 10","omim","603516"
> "0111253","neurofibromatosis 1","omim","162200"
14182a28891,28892
> "0111264","Ruijs-Aalfs syndrome","omim","616200"
> "0080128","mitochondrial DNA depletion syndrome 9","omim","245400"
14183a28894,28896
> "0080042","autosomal recessive spinocerebellar ataxia 18","omim","616204"
> "0050883","infantile cerebellar-retinal degeneration","omim","614559"
> "0080445","early infantile epileptic encephalopathy 13","omim","614558"
14187c28900,28902
< "0060227","Adams-Oliver syndrome","omim","614219"
---
> "0110402","retinitis pigmentosa 45","omim","613767"
> "0110256","cataract 21 multiple types","omim","610202"
> "0111511","melanoma and neural system tumor syndrome","omim","155755"
14189a28905,28906
> "0110629","Wolfram syndrome 1","omim","222300"
> "12185","otosclerosis","omim","611572"
14191c28908,28909
< "0050428","nonepidermolytic palmoplantar keratoderma","omim","615735"
---
> "0111490","combined oxidative phosphorylation deficiency 26","omim","616539"
> "0080053","Albright's hereditary osteodystrophy","omim","103580"
14194c28912
< "0111107","maturity-onset diabetes of the young type 9","omim","612225"
---
> "0050633","ocular albinism","omim","300500"
14196c28914,28916
< "9164","achalasia","omim","200400"
---
> "10608","celiac disease","omim","611598"
> "4428","dyslexia","omim","300509"
> "0111295","generalized epilepsy with febrile seizures plus 7","omim","613863"
14198c28918,28921
< "2058","chronic mucocutaneous candidiasis","omim","114580"
---
> "11830","myopia","omim","609258"
> "5374","pilomatrixoma","omim","132600"
> "0110567","autosomal dominant nonsyndromic deafness 41","omim","608224"
> "13884","sick sinus syndrome","omim","163800"
14200c28923,28924
< "0060384","acrofacial dysostosis, Catania type","omim","101805"
---
> "0060251","sclerosteosis","omim","269500"
> "2452","thrombophilia","omim","614486"
14202,14204c28926
< "11830","myopia","omim","609257"
< "0060169","benign familial infantile epilepsy","omim","605751"
< "0070147","hereditary sensory neuropathy type 2C","omim","614213"
---
> "4154","dentinogenesis imperfecta","omim","125500"
14206c28928,28930
< "0050576","Senior-Loken syndrome","omim","609254"
---
> "0110938","autosomal dominant osteopetrosis 2","omim","166600"
> "0111415","trichohepatoenteric syndrome 1","omim","222470"
> "14679","VACTERL association","omim","276950"
14208c28932,28933
< "0110596","primary ciliary dyskinesia 21","omim","615294"
---
> "0060273","pontocerebellar hypoplasia type 4","omim","225753"
> "13137","Werdnig-Hoffmann disease","omim","253300"
14209a28935
> "13269","hereditary coproporphyria","omim","121300"
14211,14212c28937,28941
< "0060285","parietal foramina","omim","609597"
< "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","omim","241410"
---
> "0110284","autosomal recessive limb-girdle muscular dystrophy type 2L","omim","611307"
> "14723","beta-ketothiolase deficiency","omim","203750"
> "0050795","cone dystrophy","omim","610478"
> "0111580","Behr syndrome","omim","210000"
> "12934","Kearns-Sayre syndrome","omim","530000"
14214a28944
> "0080539","PEHO syndrome","omim","260565"
14216c28946
< "1339","Diamond-Blackfan anemia","omim","613308"
---
> "1339","Diamond-Blackfan anemia","omim","105650"
14218,14220c28948,28951
< "0070061","autosomal dominant non-syndromic intellectual disability 31","omim","616158"
< "0110082","arrhythmogenic right ventricular dysplasia 11","omim","610476"
< "1094","attention deficit hyperactivity disorder","omim","612312"
---
> "0060280","primary pigmented nodular adrenocortical disease","omim","610475"
> "0050566","X-linked nonsyndromic deafness","omim","304500"
> "0060428","chromosome 2q32-q33 deletion syndrome","omim","612313"
> "0060886","osteopathia striata with cranial sclerosis","omim","300373"
14222c28953
< "0110938","autosomal dominant osteopetrosis 2","omim","166600"
---
> "5426","premature ovarian failure","omim","612310"
14224a28956,28957
> "7765","Coats disease","omim","300216"
> "0111451","progressive myoclonus epilepsy 8","omim","616230"
14225a28959,28960
> "0050453","lissencephaly","omim","300215"
> "12387","nephrogenic diabetes insipidus","omim","125800"
14227c28962
< "0060289","Ohdo syndrome","omim","249620"
---
> "9406","hypopituitarism","omim","262700"
14229,14230c28964,28969
< "0110754","type 1 diabetes mellitus 17","omim","603266"
< "0111027","hemochromatosis type 2A","omim","602390"
---
> "0080155","very long chain acyl-CoA dehydrogenase deficiency","omim","201475"
> "0080228","autosomal dominant mental retardation 53","omim","617798"
> "0080230","autosomal dominant mental retardation 54","omim","617799"
> "0080154","short chain acyl-CoA dehydrogenase deficiency","omim","201470"
> "2908","Treacher Collins syndrome","omim","154500"
> "0080231","autosomal dominant mental retardation 52","omim","617796"
14234a28974,28975
> "0070113","Niemann-Pick disease type C1","omim","257220"
> "0111366","familial hepatic adenoma","omim","142330"
14235a28977,28979
> "0111559","Charcot-Marie-Tooth disease type 2EE","omim","618400"
> "0110047","Alzheimer's disease 14","omim","611154"
> "0111576","dehydrated hereditary stomatocytosis 1","omim","194380"
14238a28983
> "0111222","centronuclear myopathy 5","omim","615959"
14240,14242c28985,28993
< "0110096","short-rib thoracic dysplasia 14 with polydactyly","omim","616546"
< "0111007","X-linked cone-rod dystrophy 3","omim","300476"
< "0110894","inflammatory bowel disease 11","omim","191390"
---
> "0111343","lateral meningocele syndrome","omim","130720"
> "0080270","autosomal dominant nonsyndromic deafness 34","omim","617772"
> "0080239","autosomal recessive mental retardation 61","omim","617773"
> "0080288","spinocerebellar ataxia 46","omim","617770"
> "0080284","early infantile epileptic encephalopathy 57","omim","617771"
> "14557","primary pulmonary hypertension","omim","178600"
> "0111254","glutaric acidemia I","omim","231670"
> "0050585","congenital generalized lipodystrophy","omim","608594"
> "0050980","spinocerebellar ataxia type 31","omim","117210"
14246,14250c28997,29003
< "0110103","atopic dermatitis 7","omim","613064"
< "0060851","pemphigus vulgaris","omim","169610"
< "0111058","platelet-type bleeding disorder 12","omim","605735"
< "11555","Fuchs' endothelial dystrophy","omim","613271"
< "11555","Fuchs' endothelial dystrophy","omim","613270"
---
> "0110389","retinitis pigmentosa 73","omim","616544"
> "0111181","familial hemiplegic migraine 1","omim","141500"
> "0080327","multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly","omim","236500"
> "0050693","Brooke-Spiegler syndrome","omim","605041"
> "5806","stork bite","omim","163100"
> "0110418","retinitis pigmentosa Y-linked","omim","400004"
> "0080046","Stickler syndrome","omim","604841"
14252c29005,29007
< "0070229","intrahepatic cholestasis of pregnancy 3","omim","614972"
---
> "0080593","orofacial cleft 6","omim","608864"
> "0060733","junctional epidermolysis bullosa with pyloric atresia","omim","226730"
> "0050575","D-2-hydroxyglutaric aciduria","omim","600721"
14254,14255c29009,29010
< "10608","celiac disease","omim","612008"
< "10608","celiac disease","omim","612007"
---
> "0060234","Carpenter syndrome","omim","614976"
> "0090043","dystonia 5","omim","128230"
14258a29014,29015
> "0080446","early infantile epileptic encephalopathy 66","omim","618067"
> "0090056","dystonia 12","omim","128235"
14260c29017
< "0060833","Griscelli syndrome type 2","omim","607624"
---
> "0070029","ITM2B-related cerebral amyloid angiopathy 1","omim","176500"
14262,14264c29019,29023
< "10608","celiac disease","omim","609754"
< "0110844","xeroderma pigmentosum group C","omim","278720"
< "14448","46 XY gonadal dysgenesis","omim","400044"
---
> "0050646","distal arthrogryposis","omim","121050"
> "1339","Diamond-Blackfan anemia","omim","615909"
> "2580","rhizomelic chondrodysplasia punctata","omim","215100"
> "0111319","idiopathic generalized epilepsy 4","omim","609750"
> "10629","microphthalmia","omim","300166"
14266a29026
> "0060434","chromosome 17q21.31 duplication syndrome","omim","613533"
14268c29028,29030
< "0070186","Y-linked spermatogenic failure 1","omim","400042"
---
> "0080517","Meier-Gorlin syndrome 6","omim","616835"
> "2340","craniosynostosis","omim","182212"
> "0111517","autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2","omim","609283"
14270c29032,29033
< "0060839","isolated microphthalmia 2","omim","610093"
---
> "0110926","nemaline myopathy 1","omim","609284"
> "0111329","pyridoxamine 5'-phosphate oxidase deficiency","omim","610090"
14272c29035,29039
< "5426","premature ovarian failure","omim","300511"
---
> "0110995","Joubert syndrome 26","omim","616784"
> "0110082","arrhythmogenic right ventricular dysplasia 11","omim","610476"
> "14720","type I Ehlers-Danlos syndrome","omim","130000"
> "11367","congenital aphakia","omim","610256"
> "1067","open-angle glaucoma","omim","603383"
14273a29041,29042
> "0080339","familial erythrocytosis 4","omim","611783"
> "0060742","methylmalonic acidemia cblA type","omim","251100"
14274a29044
> "0111236","congenital muscular dystrophy-dystroglycanopathy type A3","omim","253280"
14277c29047
< "0111098","Fanconi anemia complementation group B","omim","300514"
---
> "0110994","Joubert syndrome 25","omim","616781"
14279c29049
< "0060688","arteriovenous malformations of the brain","omim","108010"
---
> "0060536","mitochondrial complex I deficiency","omim","252010"
14280a29051
> "12449","aplastic anemia","omim","609135"
14284a29056,29057
> "0060892","late onset Parkinson's disease","omim","168600"
> "0050983","spinocerebellar ataxia type 36","omim","614153"
14285a29059
> "0080088","nonsyndromic congenital nail disorder 10","omim","614157"
14290a29065,29067
> "0080567","congenital disorder of glycosylation Ip","omim","613661"
> "0080123","mitochondrial DNA depletion syndrome 4b","omim","613662"
> "0111535","progressive osseous heteroplasia","omim","166350"
14292c29069,29070
< "0110952","Waardenburg syndrome type 2D","omim","608890"
---
> "0110782","hereditary spastic paraplegia 31","omim","610250"
> "0110363","retinitis pigmentosa 71","omim","616394"
14295,14297c29073,29076
< "0070068","autosomal dominant non-syndromic intellectual disability 38","omim","616393"
< "0110191","Charcot-Marie-Tooth disease type 4B1","omim","601382"
< "14711","FG syndrome","omim","305450"
---
> "2476","hereditary spastic paraplegia","omim","303350"
> "1339","Diamond-Blackfan anemia","omim","606129"
> "0070071","autosomal dominant non-syndromic intellectual disability 41","omim","616944"
> "3246","embryonal rhabdomyosarcoma","omim","268210"
14299,14300c29078,29082
< "0110467","autosomal recessive nonsyndromic deafness 12","omim","601386"
< "0080068","Charcot-Marie-Tooth disease type 6","omim","601152"
---
> "0060685","autosomal dominant nocturnal frontal lobe epilepsy 4","omim","610353"
> "0111532","osteoglophonic dysplasia","omim","166250"
> "0060271","pontocerebellar hypoplasia type 2E","omim","615851"
> "0060759","immunodeficiency with hyper IgM type 5","omim","608106"
> "10608","celiac disease","omim","612008"
14303c29085
< "206","hereditary multiple exostoses","omim","133701"
---
> "0050786","iridogoniodysgenesis syndrome","omim","601631"
14305,14307c29087,29091
< "0110965","brachydactyly type A2","omim","112600"
< "0060367","autosomal dominant Parkinson's disease 1","omim","168601"
< "0070280","primary autosomal recessive microcephaly 5","omim","608716"
---
> "0080074","neural tube defect","omim","601634"
> "2775","long bone adamantinoma","omim","102660"
> "0060334","transient neonatal diabetes mellitus","omim","601410"
> "0060578","Noonan syndrome 1","omim","163950"
> "2738","pseudoxanthoma elasticum","omim","264800"
14309c29093
< "12132","granulomatosis with polyangiitis","omim","608710"
---
> "0110356","retinitis pigmentosa 18","omim","601414"
14310a29095
> "12185","otosclerosis","omim","608244"
14312a29098
> "9827","radioulnar synostosis","omim","179300"
14314a29101,29102
> "0110812","hereditary spastic paraplegia 61","omim","615685"
> "2746","glycogen storage disease V","omim","232600"
14318,14319c29106,29107
< "10825","essential hypertension","omim","610262"
< "0110518","autosomal recessive nonsyndromic deafness 67","omim","610265"
---
> "10608","celiac disease","omim","612007"
> "0050989","episodic ataxia type 1","omim","160120"
14321c29109
< "0070018","autosomal dominant dyskeratosis congenita 3","omim","613990"
---
> "0060710","autosomal recessive congenital ichthyosis 2","omim","242100"
14323c29111
< "0070148","hereditary sensory neuropathy type 1B","omim","608088"
---
> "0080449","early infantile epileptic encephalopathy 16","omim","615338"
14325c29113,29116
< "14289","Ebstein anomaly","omim","224700"
---
> "0050793","short QT syndrome","omim","609621"
> "0050793","short QT syndrome","omim","609620"
> "8757","gastric mucosal hypertrophy","omim","137280"
> "0090059","enhanced S-cone syndrome","omim","268100"
14328d29118
< "0060161","Kennedy's disease","omim","313200"
14332c29122,29124
< "0070218","familial hyperinsulinemic hypoglycemia 2","omim","601820"
---
> "14500","fucosidosis","omim","230000"
> "206","hereditary multiple exostoses","omim","133701"
> "10629","microphthalmia","omim","309801"
14339c29131,29132
< "3962","follicular thyroid carcinoma","omim","188470"
---
> "0050433","fatal familial insomnia","omim","600072"
> "3962","thyroid gland follicular carcinoma","omim","188470"
14340a29134
> "0050992","episodic ataxia type 4","omim","606552"
14341a29136,29137
> "0050991","episodic ataxia type 3","omim","606554"
> "12714","Ellis-Van Creveld syndrome","omim","225500"
14342a29139
> "14725","autosomal dominant microcephaly","omim","156580"
14347a29145
> "0070209","hereditary lymphedema ID","omim","615907"
14349a29148,29149
> "0110494","autosomal recessive nonsyndromic deafness 36","omim","609006"
> "14735","hereditary angioedema","omim","106100"
14351a29152
> "0080453","early infantile epileptic encephalopathy 25","omim","615905"
14354c29155,29156
< "0110346","osteogenesis imperfecta type 10","omim","613848"
---
> "9649","congenital nystagmus","omim","193003"
> "0110162","Charcot-Marie-Tooth disease, axonal type 2W","omim","616625"
14359c29161
< "14793","hypohidrotic ectodermal dysplasia","omim","129490"
---
> "0110528","autosomal recessive nonsyndromic deafness 83","omim","613685"
14361a29164,29165
> "0111471","combined oxidative phosphorylation deficiency 30","omim","616974"
> "0060458","chromosome 2q31.1 duplication syndrome","omim","613681"
14363c29167
< "0070204","familial partial lipodystrophy type 3","omim","604367"
---
> "0110972","brachydactyly type E1","omim","113300"
14364a29169,29170
> "0050604","acrocapitofemoral dysplasia","omim","607778"
> "0070248","autosomal recessive Emery-Dreifuss muscular dystrophy 3","omim","616516"
14366a29173,29175
> "0111345","transient bullous dermolysis of the newborn","omim","131705"
> "13481","thanatophoric dysplasia","omim","273680"
> "0090083","hypogonadotropic hypogonadism 2 with or without anosmia","omim","147950"
14370d29178
< "0070269","congenital disorder of glycosylation type IIq","omim","617395"
14372d29179
< "0111156","spermatogenic failure 9","omim","613958"
14379,14381c29186,29191
< "0110559","autosomal dominant nonsyndromic deafness 2B","omim","612644"
< "0110565","autosomal dominant nonsyndromic deafness 3B","omim","612643"
< "0110583","autosomal dominant nonsyndromic deafness 59","omim","612642"
---
> "0070073","autosomal dominant non-syndromic intellectual disability 43","omim","616977"
> "0111371","isolated hyperchlorhidrosis","omim","143860"
> "2920","membranoproliferative glomerulonephritis","omim","305800"
> "0110191","Charcot-Marie-Tooth disease type 4B1","omim","601382"
> "3393","coronary artery disease","omim","611139"
> "11252","microcytic anemia","omim","206200"
14383a29194
> "0060386","Chilblain lupus","omim","614415"
14385a29197
> "0111574","autosomal recessive woolly hair 3","omim","616760"
14386a29199
> "11486","Horner's syndrome","omim","143000"
14390c29203,29205
< "11819","ureter cancer","omim","191600"
---
> "0060805","Prieto syndrome","omim","309610"
> "0060295","complement component 2 deficiency","omim","217000"
> "0110815","hereditary spastic paraplegia 64","omim","615683"
14394a29210
> "0080350","retinitis pigmentosa 77","omim","617304"
14396a29213,29214
> "10487","Hirschsprung's disease","omim","606874"
> "9884","muscular dystrophy","omim","309930"
14399c29217
< "0080415","early infantile epileptic encephalopathy 23","omim","615859"
---
> "0090038","torsion dystonia 2","omim","224500"
14400a29219
> "14679","VACTERL association","omim","192350"
14401a29221,29222
> "8445","intestinal volvulus","omim","193250"
> "0060347","acrorenal syndrome","omim","201310"
14404,14405c29225,29233
< "2224","essential thrombocythemia","omim","614521"
< "12801","mucopolysaccharidosis III","omim","252920"
---
> "0110910","leukocyte adhesion deficiency 1","omim","116920"
> "0111485","combined oxidative phosphorylation deficiency 24","omim","616239"
> "13375","temporal arteritis","omim","187360"
> "0060431","chromosome 16p13.3 duplication syndrome","omim","613458"
> "0060433","chromosome 17q12 duplication syndrome","omim","614526"
> "0060404","chromosome 17q12 deletion syndrome","omim","614527"
> "0060465","fibrochondrogenesis","omim","614524"
> "0111394","mucopolysaccharidosis type IIIB","omim","252920"
> "0111292","idiopathic generalized epilepsy 10","omim","613060"
14407,14408c29235,29236
< "11830","myopia","omim","609259"
< "0110389","retinitis pigmentosa 73","omim","616544"
---
> "0110096","short-rib thoracic dysplasia 14 with polydactyly","omim","616546"
> "0110103","atopic dermatitis 7","omim","613064"
14409a29238
> "0080537","hypermanganesemia with dystonia 2","omim","617013"
14410a29240,29242
> "0050719","cerebral folate receptor alpha deficiency","omim","613068"
> "0080592","Klippel-Feil syndrome 3","omim","616549"
> "0080592","Klippel-Feil syndrome 4","omim","616549"
14412,14413c29244,29246
< "0110995","Joubert syndrome 26","omim","616784"
< "1067","open-angle glaucoma","omim","603383"
---
> "0090045","childhood onset GLUT1 deficiency syndrome 2","omim","612126"
> "5426","premature ovarian failure","omim","300511"
> "0080494","ovarian dysgenesis 2","omim","300510"
14416c29249
< "0110994","Joubert syndrome 25","omim","616781"
---
> "0111098","Fanconi anemia complementation group B","omim","300514"
14418c29251
< "0110897","inflammatory bowel disease 15","omim","612255"
---
> "0050681","Borjeson-Forssman-Lehmann syndrome","omim","301900"
14421c29254,29256
< "0110896","inflammatory bowel disease 16","omim","612259"
---
> "0110952","Waardenburg syndrome type 2D","omim","608890"
> "0080408","orofacial cleft 15","omim","616788"
> "0111373","familial progressive hyperpigmentation with or without hypopigmentation","omim","145250"
14423c29258,29260
< "0060287","cornea plana","omim","217300"
---
> "0111348","multiple epiphyseal dysplasia with myopia and deafness","omim","132450"
> "0060342","acromelic frontonasal dysostosis","omim","603671"
> "0111544","Guttmacher syndrome","omim","176305"
14425,14426c29262,29265
< "10629","microphthalmia","omim","309801"
< "1156","chondrocalcinosis","omim","118600"
---
> "0080307","myofibrillar myopathy","omim","601419"
> "0070121","Meckel syndrome 7","omim","267010"
> "0110469","autosomal recessive nonsyndromic deafness 14","omim","603678"
> "2216","factor V deficiency","omim","227400"
14427a29267,29268
> "0111374","selective pituitary thyroid hormone resistance","omim","145650"
> "13945","CADASIL","omim","600142"
14428a29270
> "12236","primary biliary cirrhosis","omim","613008"
14433a29276,29277
> "0110755","type 1 diabetes mellitus 18","omim","605598"
> "14450","46 XX gonadal dysgenesis","omim","233300"
14434a29279
> "12712","nephronophthisis","omim","256100"
14435a29281
> "0111445","progressive myoclonus epilepsy 10","omim","616640"
14437a29284
> "1588","thrombocytopenia","omim","313900"
14441,14442c29288,29291
< "0060792","hypomyelinating leukodystrophy 11","omim","616494"
< "0110972","brachydactyly type E1","omim","113300"
---
> "9884","muscular dystrophy","omim","159050"
> "0110589","autosomal dominant nonsyndromic deafness 68","omim","616707"
> "0070250","autosomal dominant Emery-Dreifuss muscular dystrophy 5","omim","612999"
> "14773","cartilage-hair hypoplasia","omim","250250"
14443a29293,29297
> "0070111","Niemann-Pick disease type A","omim","257200"
> "0110829","retinitis pigmentosa-deafness syndrome","omim","500004"
> "0080503","multiple congenital anomalies-hypotonia-seizures syndrome","omim","614080"
> "0080232","autosomal dominant mental retardation 51","omim","617788"
> "0111273","NARP syndrome","omim","551500"
14445,14446c29299,29301
< "0110609","primary ciliary dyskinesia 23","omim","615451"
< "0060213","FTDALS1","omim","105550"
---
> "0080542","hyperprolinemia type 1","omim","239500"
> "0080272","nephrotic syndrome type 16","omim","617783"
> "0060483","MEDNIK syndrome","omim","609313"
14447a29303,29304
> "0080045","Kniest dysplasia","omim","156550"
> "0080491","cerebral cavernous malformation 1","omim","116860"
14449,14450c29306,29307
< "10595","Charcot-Marie-Tooth disease","omim","118220"
< "14264","benign neonatal seizures","omim","121200"
---
> "0080456","early infantile epileptic encephalopathy 46","omim","617162"
> "0110644","long QT syndrome 1","omim","192500"
14451a29309,29310
> "0080425","early infantile epileptic encephalopathy 47","omim","617166"
> "2842","Jervell-Lange Nielsen syndrome","omim","220400"
14453,14454c29312,29316
< "0110066","amelogenesis imperfecta type 1G","omim","204690"
< "0110805","hereditary spastic paraplegia 53","omim","614898"
---
> "0070249","autosomal dominant Emery-Dreifuss muscular dystrophy 4","omim","612998"
> "0070274","hereditary nonpolyposis colorectal cancer type 2","omim","609310"
> "0111385","inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1","omim","167320"
> "3132","porphyria cutanea tarda","omim","176100"
> "0080279","Joubert syndrome 33","omim","617767"
14456c29318,29322
< "0110141","Bardet-Biedl syndrome 19","omim","615996"
---
> "0080277","Joubert syndrome 31","omim","617761"
> "0111221","centronuclear myopathy 6 with fiber-type disproportion","omim","617760"
> "0060792","hypomyelinating leukodystrophy 11","omim","616494"
> "0080287","spinocerebellar ataxia 45","omim","617769"
> "0090080","hypogonadotropic hypogonadism 16 with or without anosmia","omim","614897"
14457a29324
> "0111423","branchiootorenal syndrome 1","omim","113650"
14458a29326
> "14756","autosomal dominant type IV Ehlers-Danlos syndrome","omim","130050"
14459a29328
> "0111505","palmoplantar keratoderma-deafness syndrome","omim","148350"
14461c29330
< "0110640","congenital muscular dystrophy due to LMNA mutation","omim","613205"
---
> "0110136","Bardet-Biedl syndrome 14","omim","615991"
14463a29333
> "0080029","autosomal recessive spinocerebellar ataxia 16","omim","615768"
14465,14468c29335,29341
< "2224","essential thrombocythemia","omim","300331"
< "0110474","autosomal recessive nonsyndromic deafness 18B","omim","614945"
< "0060485","Mowat-Wilson syndrome","omim","235730"
< "0070331","mitochondrial DNA depletion syndrome 8b","omim","612075"
---
> "0110530","autosomal recessive nonsyndromic deafness 84B","omim","614944"
> "0080124","mitochondrial DNA depletion syndrome 5","omim","612073"
> "0111477","combined oxidative phosphorylation deficiency 14","omim","614946"
> "0111491","combined oxidative phosphorylation deficiency 15","omim","614947"
> "0060283","peeling skin syndrome","omim","270300"
> "3156","hypomelanosis of Ito","omim","300337"
> "0080127","mitochondrial DNA depletion syndrome 8a","omim","612075"
14469a29343
> "0111479","combined oxidative phosphorylation deficiency 8","omim","614096"
14470a29345,29347
> "1312","focal segmental glomerulosclerosis","omim","603278"
> "11830","myopia","omim","255500"
> "0080033","craniometaphyseal dysplasia","omim","614099"
14472,14473c29349,29351
< "0060735","epidermolysis bullosa simplex Dowling-Meara type","omim","131760"
< "0080398","orofacial cleft 4","omim","608371"
---
> "0090135","complex cortical dysplasia with other brain malformations 5","omim","615763"
> "0110883","inflammatory bowel disease 17","omim","612261"
> "14498","lipoid proteinosis","omim","247100"
14478c29356
< "0110356","retinitis pigmentosa 18","omim","601414"
---
> "0050684","Bowen-Conradi syndrome","omim","211180"
14480,14482c29358,29361
< "10908","hydrocephalus","omim","236600"
< "0050710","3-Methylcrotonyl-CoA carboxylase deficiency","omim","210210"
< "0110769","hereditary spastic paraplegia 16","omim","300266"
---
> "0111529","familial multiple nevi flammei","omim","163000"
> "0110116","autoimmune lymphoproliferative syndrome type 2B","omim","607271"
> "0080580","3-Methylcrotonyl-CoA carboxylase 2 deficiency","omim","210210"
> "0060238","Van Maldergem syndrome","omim","601390"
14483a29363
> "0111528","Naegeli-Franceschetti-Jadassohn syndrome","omim","161000"
14491c29371
< "0110698","hypotrichosis 1","omim","605389"
---
> "8691","mycosis fungoides","omim","254400"
14493d29372
< "0110547","autosomal dominant nonsyndromic deafness 16","omim","603964"
14494a29374
> "1324","lung cancer","omim","211980"
14497,14498c29377,29380
< "0060641","endocrine-cerebro-osteodysplasia syndrome","omim","612651"
< "1040","chronic lymphocytic leukemia","omim","151400"
---
> "0111247","hypertension and brachydactyly syndrome","omim","112410"
> "0110609","primary ciliary dyskinesia 23","omim","615451"
> "2235","prothrombin deficiency","omim","613679"
> "0050690","brachyolmia","omim","613678"
14500,14501c29382,29386
< "0060238","Van Maldergem syndrome","omim","601390"
< "1338","congenital dyserythropoietic anemia","omim","613673"
---
> "0080121","mitochondrial DNA depletion syndrome 3","omim","251880"
> "14669","acrodysostosis","omim","101800"
> "0110505","autosomal recessive nonsyndromic deafness 48","omim","609439"
> "0111400","congenital dyserythropoietic anemia type IV","omim","613673"
> "0050943","spastic ataxia 4","omim","613672"
14505a29391
> "0060403","chromosome 17q11.2 deletion syndrome, 1.4Mb","omim","613675"
14507a29394
> "13042","persistent fetal circulation syndrome","omim","265380"
14510c29397
< "0050650","familial atrial fibrillation","omim","613980"
---
> "2340","craniosynostosis","omim","600593"
14512,14514c29399,29409
< "0070172","spermatogenic failure 15","omim","616950"
< "0110975","brachydactyly type B2","omim","611377"
< "2121","ectodermal dysplasia","omim","305100"
---
> "0080233","autosomal dominant mental retardation 50","omim","617787"
> "0080438","early infantile epileptic encephalopathy 5","omim","613477"
> "9432","renal glycosuria","omim","233100"
> "0080409","familial adenomatous polyposis 1","omim","175100"
> "2861","congenital nonspherocytic hemolytic anemia","omim","613470"
> "0110493","autosomal recessive nonsyndromic deafness 35","omim","608565"
> "11830","myopia","omim","609257"
> "2571","Langerhans-cell histiocytosis","omim","604856"
> "332","amyotrophic lateral sclerosis","omim","105400"
> "10587","Krabbe disease","omim","245200"
> "10629","microphthalmia","omim","615972"
14517a29413,29414
> "0110534","autosomal recessive nonsyndromic deafness 89","omim","613916"
> "1062","Fanconi syndrome","omim","134600"
14519a29417
> "10595","Charcot-Marie-Tooth disease","omim","118220"
14521c29419,29423
< "9406","hypopituitarism","omim","613986"
---
> "0111525","autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4","omim","610131"
> "0070224","progressive familial intrahepatic cholestasis 4","omim","615878"
> "0111473","combined oxidative phosphorylation deficiency 5","omim","611719"
> "14264","benign neonatal seizures","omim","121200"
> "0080562","congenital disorder of glycosylation Ij","omim","608093"
14525c29427,29428
< "0060755","familial temporal lobe epilepsy 2","omim","608096"
---
> "0050449","pachyonychia congenita","omim","167200"
> "0070019","autosomal recessive dyskeratosis congenita 3","omim","613988"
14527c29430
< "0110278","autosomal recessive limb-girdle muscular dystrophy type 2D","omim","608099"
---
> "0080426","early infantile epileptic encephalopathy 63","omim","617976"
14529c29432
< "0110782","hereditary spastic paraplegia 31","omim","610250"
---
> "0080415","early infantile epileptic encephalopathy 23","omim","615859"
14531,14533c29434,29438
< "0060352","Kleefstra syndrome","omim","610253"
< "0110021","age related macular degeneration 9","omim","611378"
< "8986","narcolepsy","omim","614223"
---
> "699","mitochondrial myopathy","omim","251900"
> "0070179","spermatogenic failure 14","omim","615842"
> "1067","open-angle glaucoma","omim","608695"
> "0070058","Helsmoortel-Van Der Aa Syndrome","omim","615873"
> "12716","newborn respiratory distress syndrome","omim","267450"
14537c29442
< "0060387","chondrodysplasia Blomstrand type","omim","215045"
---
> "13482","Proteus syndrome","omim","176920"
14539c29444
< "0110964","brachydactyly type A1","omim","112500"
---
> "0110066","amelogenesis imperfecta type 1G","omim","204690"
14543c29448
< "0070043","autosomal dominant non-syndromic intellectual disability 13","omim","614563"
---
> "0110209","Charcot-Marie-Tooth disease X-linked dominant 1","omim","302800"
14544a29450
> "0080329","cold-induced sweating syndrome 1","omim","272430"
14548,14549c29454,29456
< "12802","mucopolysaccharidosis I","omim","607014"
< "12802","mucopolysaccharidosis I","omim","607015"
---
> "3261","hyper IgE recurrent infection syndrome 1","omim","147060"
> "0111389","mucopolysaccharidosis Ih/s","omim","607015"
> "0110718","Warburg micro syndrome 3","omim","614222"
14550a29458
> "2058","chronic mucocutaneous candidiasis","omim","114580"
14553c29461
< "0110272","cataract 40","omim","302200"
---
> "0070202","familial partial lipodystrophy type 2","omim","151660"
14556c29464,29466
< "0110431","dilated cardiomyopathy 1I","omim","604765"
---
> "0050762","adenylosuccinase lyase deficiency","omim","103050"
> "0110174","Charcot-Marie-Tooth disease axonal type 2L","omim","608673"
> "0110909","inflammatory bowel disease 25","omim","612567"
14557a29468,29469
> "0111351","D-2-hydroxyglutaric aciduria 1","omim","600721"
> "0080406","orofacial cleft 13","omim","613857"
14559c29471
< "10908","hydrocephalus","omim","615219"
---
> "0050993","episodic ataxia type 5","omim","613855"
14561c29473
< "0110834","Usher syndrome type 1G","omim","606943"
---
> "0060557","ataxia with oculomotor apraxia type 3","omim","615217"
14563a29476
> "0110805","hereditary spastic paraplegia 53","omim","614898"
14567a29481,29482
> "0080271","nephrotic syndrome type 15","omim","617609"
> "3263","piebaldism","omim","172800"
14569c29484,29485
< "0110648","long QT syndrome 6","omim","613693"
---
> "0110338","osteogenesis imperfecta type 17","omim","616507"
> "13271","cutaneous porphyria","omim","263700"
14573d29488
< "10584","retinitis pigmentosa","omim","268000"
14574a29490
> "0111563","Sturge-Weber syndrome","omim","185300"
14576a29493,29494
> "0110449","dilated cardiomyopathy 1M","omim","607482"
> "0111218","Friedreich ataxia 1","omim","229300"
14580a29499,29500
> "0050948","autosomal dominant hypophosphatemic rickets","omim","193100"
> "0050789","tarsal-carpal coalition syndrome","omim","186570"
14582a29503,29504
> "1811","reflex sympathetic dystrophy","omim","604335"
> "1572","normal pressure hydrocephalus","omim","236690"
14583a29506
> "0080243","amelogenesis imperfecta type 3B","omim","617607"
14588a29512
> "0080267","autosomal dominant nonsyndromic deafness 71","omim","617605"
14590c29514
< "2738","pseudoxanthoma elasticum","omim","264800"
---
> "0110670","congenital myasthenic syndrome 9","omim","616325"
14591a29516,29518
> "0110793","hereditary spastic paraplegia 41","omim","613364"
> "4428","dyslexia","omim","606616"
> "0111335","myopathy with extrapyramidal signs","omim","615673"
14593a29521
> "0111163","molybdenum cofactor deficiency type B","omim","252160"
14595c29523,29525
< "0110812","hereditary spastic paraplegia 61","omim","615685"
---
> "0090053","episodic kinesigenic dyskinesia 1","omim","128200"
> "0111466","combined oxidative phosphorylation deficiency 38","omim","618378"
> "8538","reticulosarcoma","omim","267730"
14597c29527,29528
< "0110813","hereditary spastic paraplegia 62","omim","615681"
---
> "14451","hyperkalemic periodic paralysis","omim","170500"
> "0110662","congenital myasthenic syndrome 1B","omim","608930"
14599,14600c29530,29534
< "13774","Addison's disease","omim","103230"
< "0060739","hand-foot-genital syndrome","omim","140000"
---
> "0060651","MYH-9 related disease","omim","155100"
> "0050642","hypochromic microcytic anemia","omim","206100"
> "0111386","inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3","omim","615424"
> "0080033","craniometaphyseal dysplasia","omim","123000"
> "0110004","3-methylglutaconic aciduria type 3","omim","258501"
14601a29536,29537
> "0060253","scapuloperoneal myopathy","omim","181430"
> "0080125","mitochondrial DNA depletion syndrome 6","omim","256810"
14603c29539,29540
< "0050588","muscular dystrophy-dystroglycanopathy","omim","615041"
---
> "0111239","congenital muscular dystrophy-dystroglycanopathy type A10","omim","615041"
> "990","congenital heart block","omim","234700"
14608c29545
< "0111103","maturity-onset diabetes of the young type 4","omim","606392"
---
> "1339","Diamond-Blackfan anemia","omim","612528"
14612c29549,29550
< "1882","atrial heart septal defect","omim","108800"
---
> "0080587","congenital myasthenic syndrome 22","omim","616224"
> "0080528","bronchiectasis 3","omim","613071"
14616,14617c29554,29557
< "5520","head and neck squamous cell carcinoma","omim","275355"
< "0060587","Noonan syndrome 9","omim","616559"
---
> "0110618","primary ciliary dyskinesia 13","omim","613193"
> "0110480","autosomal recessive nonsyndromic deafness 22","omim","607039"
> "0050995","episodic ataxia type 7","omim","611907"
> "0080258","autosomal recessive congenital ichthyosis 14","omim","617571"
14619,14620c29559,29561
< "0050524","maturity-onset diabetes of the young","omim","606391"
< "0110872","holoprosencephaly 2","omim","157170"
---
> "0111392","mucopolysaccharidosis type IVB","omim","253010"
> "0080257","autosomal recessive congenital ichthyosis 13","omim","617574"
> "0080265","nephrotic syndrome type 14","omim","617575"
14621a29563
> "0080266","primary ciliary dyskinesia 37","omim","617577"
14623a29566
> "0060389","chromosome 10q23 deletion syndrome","omim","612242"
14627,14628c29570,29571
< "2987","familial Mediterranean fever","omim","134610"
< "0050818","transcobalamin II deficiency","omim","275350"
---
> "11044","gastroschisis","omim","230750"
> "1040","chronic lymphocytic leukemia","omim","109543"
14629a29573,29574
> "0110640","congenital muscular dystrophy due to LMNA mutation","omim","613205"
> "0111306","familial febrile seizures 5","omim","609255"
14631c29576
< "0070254","congenital disorder of glycosylation type IIb","omim","606056"
---
> "0050631","Allan-Herndon-Dudley syndrome","omim","300523"
14633,14634c29578,29580
< "0060013","X-linked severe combined immunodeficiency","omim","300400"
< "0080480","peroxisome biogenesis disorder 5A","omim","614866"
---
> "1339","Diamond-Blackfan anemia","omim","612527"
> "3635","congenital myasthenic syndrome","omim","601462"
> "1067","open-angle glaucoma","omim","602429"
14636a29583,29585
> "0111405","Fraser syndrome 1","omim","219000"
> "0111476","combined oxidative phosphorylation deficiency 19","omim","615595"
> "0080572","congenital disorder of glycosylation Iw","omim","615596"
14640c29589
< "0110681","congenital myasthenic syndrome 2A","omim","616313"
---
> "0060240","UV-sensitive syndrome","omim","614621"
14643c29592,29594
< "10126","keratoconus","omim","614629"
---
> "0111201","distal hereditary motor neuronopathy type 7A","omim","158580"
> "980","choroidal sclerosis","omim","215500"
> "0060888","transient myeloproliferative syndrome","omim","159595"
14645c29596
< "0080479","peroxisome biogenesis disorder 4A","omim","614862"
---
> "4362","cervical cancer","omim","603956"
14648,14650c29599,29604
< "0110519","autosomal recessive nonsyndromic deafness 68","omim","610419"
< "0110890","inflammatory bowel disease 19","omim","612278"
< "0110530","autosomal recessive nonsyndromic deafness 84B","omim","614944"
---
> "0080105","microcephaly and chorioretinopathy 1","omim","251270"
> "0090062","familial cold autoinflammatory syndrome 1","omim","120100"
> "0080242","syndromic X-linked mental retardation Hough type","omim","301008"
> "2224","essential thrombocythemia","omim","300331"
> "2121","ectodermal dysplasia","omim","305100"
> "0110474","autosomal recessive nonsyndromic deafness 18B","omim","614945"
14652a29607
> "12800","mucopolysaccharidosis VI","omim","253200"
14653a29609,29610
> "0111301","generalized epilepsy with febrile seizures plus 9","omim","616172"
> "0080106","microcephaly and chorioretinopathy 2","omim","616171"
14655d29611
< "0060565","Ritscher-Schinzel syndrome","omim","220210"
14657c29613
< "10426","Klippel-Feil syndrome","omim","118100"
---
> "2223","platelet storage pool deficiency","omim","185050"
14660c29616,29618
< "0111158","SADDAN","omim","616482"
---
> "0111300","generalized epilepsy with febrile seizures plus 6","omim","612279"
> "0060448","Fleck corneal dystrophy","omim","121850"
> "0060425","chromosome 8q21.11 deletion syndrome","omim","614230"
14662,14663c29620,29621
< "9074","systemic lupus erythematosus","omim","612378"
< "0110069","FTDALS4","omim","616439"
---
> "0080153","medium chain acyl-CoA dehydrogenase deficiency","omim","201450"
> "0080108","myoglobinuria","omim","550500"
14665c29623,29628
< "4990","essential tremor","omim","602134"
---
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","611097"
> "0111265","Boucher-Neuhauser syndrome","omim","215470"
> "0050605","acrodermatitis enteropathica","omim","201100"
> "0111280","psoriasis 4","omim","603935"
> "0111307","familial febrile seizures 1","omim","121210"
> "0111592","plasminogen deficiency type I","omim","217090"
14668c29631,29633
< "0060751","familial temporal lobe epilepsy 7","omim","616436"
---
> "14731","Weaver syndrome","omim","277590"
> "0080235","autosomal dominant mental retardation 48","omim","617751"
> "0080234","autosomal dominant mental retardation 49","omim","617752"
14672c29637,29640
< "0110914","infantile hypophosphatasia","omim","241500"
---
> "0080133","multiple mitochondrial dysfunctions syndrome 1","omim","605711"
> "0080278","Joubert syndrome 32","omim","617757"
> "0111214","distal spinal muscular atrophy type 5","omim","614881"
> "0090075","hypogonadotropic hypogonadism 15 with or without anosmia","omim","614880"
14675d29642
< "0110948","Waardenburg syndrome type 1","omim","193500"
14678a29646
> "0050632","oculocutaneous albinism","omim","203100"
14679a29648
> "0110475","autosomal recessive nonsyndromic deafness 1A","omim","220290"
14682,14683c29651,29652
< "0070285","primary autosomal recessive microcephaly 1","omim","251200"
< "0060776","congenital diarrhea 5 with tufting enteropathy","omim","613217"
---
> "0060432","chromosome 17p13.3 duplication syndrome","omim","613215"
> "0060611","abdominal obesity-metabolic syndrome","omim","605552"
14686,14688c29655,29662
< "10609","rickets","omim","277440"
< "0110053","amelogenesis imperfecta type 4","omim","104510"
< "10970","spastic quadriplegia","omim","612900"
---
> "0080439","early infantile epileptic encephalopathy 14","omim","614959"
> "0080346","blepharocheilodontic syndrome 2","omim","617681"
> "0060688","arteriovenous malformations of the brain","omim","108010"
> "0111453","2-aminoadipic 2-oxoadipic aciduria","omim","204750"
> "11476","osteoporosis","omim","166710"
> "0050858","Marshall-Smith syndrome","omim","602535"
> "8712","neurofibromatosis","omim","162270"
> "0080138","multiple congenital anomalies-hypotonia-seizures syndrome 1","omim","614080"
14691d29664
< "0050449","pachyonychia congenita","omim","167200"
14693c29666
< "0060233","cardiofaciocutaneous syndrome","omim","615278"
---
> "0111461","cardiofaciocutaneous syndrome 2","omim","615278"
14694a29668,29671
> "1064","cystinosis","omim","219800"
> "0060884","renal hypomagnesemia 6","omim","613882"
> "14670","hypertelorism, microtia, facial clefting syndrome","omim","239800"
> "0060282","persistent hyperplastic primary vitreous","omim","221900"
14696c29673
< "0060392","chromosome 14q11-q22 deletion syndrome","omim","613457"
---
> "0111501","combined oxidative phosphorylation deficiency 29","omim","616811"
14701c29678
< "2583","agammaglobulinemia","omim","613506"
---
> "0090140","cortisone reductase deficiency 2","omim","614662"
14705,14706c29682,29683
< "2583","agammaglobulinemia","omim","613502"
< "0111081","Fanconi anemia complementation group T","omim","616435"
---
> "0060027","agammaglobulinemia 4","omim","613502"
> "3890","acute intermittent porphyria","omim","176000"
14708c29685,29687
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","611093"
---
> "0060420","chromosome 4q21 deletion syndrome","omim","613509"
> "9884","muscular dystrophy","omim","310000"
> "0111587","Gordon Holmes syndrome","omim","212840"
14710,14712c29689,29693
< "4624","Ollier disease","omim","166000"
< "0070329","mitochondrial DNA depletion syndrome","omim","603041"
< "14448","46 XY gonadal dysgenesis","omim","300018"
---
> "6457","Cowden syndrome","omim","158350"
> "0080291","early infantile epileptic encephalopathy 59","omim","617904"
> "0060743","methylmalonic acidemia cblB type","omim","251110"
> "1270","hereditary hemorrhagic telangiectasia","omim","187300"
> "12557","Duane retraction syndrome","omim","604356"
14713a29695,29696
> "0111478","combined oxidative phosphorylation deficiency 20","omim","615917"
> "0111341","primary failure of tooth eruption","omim","125350"
14715,14716c29698,29699
< "0060730","torsion dystonia 1","omim","128100"
< "0110704","hypotrichosis 7","omim","604379"
---
> "701","dentin dysplasia","omim","125420"
> "0090041","torsion dystonia 4","omim","128101"
14718c29701,29704
< "0050576","Senior-Loken syndrome","omim","610189"
---
> "0080357","fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1","omim","604377"
> "0050772","spastic ataxia 1","omim","108600"
> "0111465","combined oxidative phosphorylation deficiency 21","omim","615918"
> "0110251","cataract 15 multiple types","omim","615274"
14719a29706
> "0050780","Opitz-GBBB syndrome","omim","300000"
14721a29709,29712
> "0111502","combined oxidative phosphorylation deficiency 6","omim","300816"
> "6498","seborrheic keratosis","omim","182000"
> "0060419","chromosome 3q29 microdeletion syndrome","omim","609425"
> "0111316","idiopathic generalized epilepsy 15","omim","618357"
14725,14726c29716
< "0050577","Sensenbrenner syndrome","omim","218330"
< "4028","angioma serpiginosum","omim","300652"
---
> "0110431","dilated cardiomyopathy 1I","omim","604765"
14728c29718,29719
< "11830","myopia","omim","609258"
---
> "0060398","chromosome 16p11.2 deletion syndrome, 220kb","omim","613444"
> "11156","anhidrosis","omim","206600"
14730c29721
< "0110971","brachydactyly type D","omim","113200"
---
> "0060341","agnathia-otocephaly complex","omim","202650"
14732a29724
> "14798","Blount's disease","omim","188700"
14734,14735c29726,29731
< "0050886","Troyer syndrome","omim","275900"
< "0050773","paraganglioma","omim","168000"
---
> "0070140","autosomal recessive cutis laxa type IIC","omim","617402"
> "0050664","Bietti crystalline corneoretinal dystrophy","omim","210370"
> "0111468","combined oxidative phosphorylation deficiency 25","omim","616430"
> "2626","choroid plexus papilloma","omim","260500"
> "0111202","distal hereditary motor neuronopathy type 7B","omim","607641"
> "0110908","inflammatory bowel disease 24","omim","612566"
14737,14739c29733,29735
< "0110497","autosomal recessive nonsyndromic deafness 39","omim","608265"
< "1540","parathyroid carcinoma","omim","608266"
< "9870","galactosemia","omim","230350"
---
> "0110030","alpha thalassemia-X-linked intellectual disability syndrome","omim","301040"
> "3756","protein C deficiency","omim","176860"
> "0111458","galactose epimerase deficiency","omim","230350"
14740a29737,29738
> "0111380","solitary median maxillary central incisor","omim","147250"
> "0080217","lysosomal and lipase deficiency","omim","278000"
14742c29740,29741
< "0110429","dilated cardiomyopathy 1H","omim","604288"
---
> "0080386","nephrotic syndrome type 10","omim","615861"
> "0111125","nephronophthisis 18","omim","615862"
14743a29743
> "0110536","autosomal recessive nonsyndromic deafness 91","omim","613453"
14745c29745
< "7004","ACTH-secreting pituitary adenoma","omim","219090"
---
> "0080071","pseudo-Hurler polydystrophy","omim","252600"
14748c29748,29749
< "0110503","autosomal recessive nonsyndromic deafness 46","omim","609647"
---
> "0050977","spinocerebellar ataxia type 28","omim","610246"
> "5684","spondyloepimetaphyseal dysplasia, Sponastrime type","omim","271510"
14752,14754c29753,29758
< "12801","mucopolysaccharidosis III","omim","252900"
< "0070192","autosomal recessive chronic granulomatous disease cytochrome b-positive type I","omim","233700"
< "10487","Hirschsprung's disease","omim","608462"
---
> "3852","Peutz-Jeghers syndrome","omim","175200"
> "0111395","mucopolysaccharidosis type IIIA","omim","252900"
> "0110421","late-adult onset retinitis pigmentosa","omim","268025"
> "10126","keratoconus","omim","614623"
> "0110557","autosomal dominant nonsyndromic deafness 28","omim","608641"
> "0110510","autosomal recessive nonsyndromic deafness 55","omim","609952"
14756a29761
> "0111238","congenital muscular dystrophy-dystroglycanopathy type A13","omim","615287"
14758c29763
< "9563","bronchiectasis","omim","211400"
---
> "0080526","bronchiectasis 1","omim","211400"
14763a29769
> "0080174","bladder exstrophy","omim","600057"
14765c29771,29773
< "0111133","focal segmental glomerulosclerosis 8","omim","616032"
---
> "0080585","Van Maldergem syndrome 1","omim","601390"
> "0111078","tibial muscular dystrophy","omim","600334"
> "0050428","nonepidermolytic palmoplantar keratoderma","omim","613000"
14769,14771c29777,29785
< "0070207","familial partial lipodystrophy type 1","omim","608600"
< "12712","nephronophthisis","omim","256100"
< "0050795","cone dystrophy","omim","610478"
---
> "0111195","erythrokeratodermia variabilis et progressiva 1","omim","133200"
> "0070069","autosomal dominant non-syndromic intellectual disability 39","omim","616521"
> "0080495","ovarian dysgenesis 3","omim","614324"
> "0111332","Pitt-Hopkins-like syndrome 2","omim","614325"
> "0060464","Feingold syndrome","omim","614326"
> "0111191","distal muscular dystrophy Tateyama type","omim","614321"
> "0080060","autosomal recessive spinocerebellar ataxia 12","omim","614322"
> "0110569","autosomal dominant nonsyndromic deafness 44","omim","607453"
> "3210","Pelizaeus-Merzbacher disease","omim","312080"
14773,14774c29787,29789
< "0110449","dilated cardiomyopathy 1M","omim","607482"
< "0110328","hypertrophic cardiomyopathy 25","omim","607487"
---
> "0090090","hypogonadotropic hypogonadism 19 with or without anosmia","omim","615269"
> "0060672","Grn-related frontotemporal lobar degeneration with Tdp43 inclusions","omim","607485"
> "9220","central sleep apnea","omim","107640"
14776a29792
> "0090035","myoclonic dystonia 15","omim","607488"
14778,14779c29794,29796
< "0060021","DNA ligase IV deficiency","omim","606593"
< "0111149","autosomal recessive isolated ectopia lentis 2","omim","225100"
---
> "288","endometriosis of uterus","omim","600458"
> "0090079","hypogonadotropic hypogonadism 17 with or without anosmia","omim","615266"
> "0090076","hypogonadotropic hypogonadism 18 with or without anosmia","omim","615267"
14781c29798
< "0110624","primary ciliary dyskinesia 30","omim","616037"
---
> "3529","central core myopathy","omim","117000"
14786c29803
< "9245","Alagille syndrome","omim","118450"
---
> "9274","hyperlysinemia","omim","238700"
14788a29806,29807
> "0080348","Alzheimer's disease 1","omim","104300"
> "0060348","hypoparathyroidism-retardation-dysmorphism syndrome","omim","241410"
14790c29809
< "0060708","lymphoproliferative syndrome 2","omim","615122"
---
> "5425","ovarian hyperstimulation syndrome","omim","608115"
14792a29812,29813
> "0111276","sensory ataxic neuropathy, dysarthria, and ophthalmoparesis","omim","607459"
> "0060244","specific language impairment","omim","607134"
14794c29815
< "0070084","schizophrenia 8","omim","603206"
---
> "0050967","spinocerebellar ataxia type 17","omim","607136"
14796c29817,29818
< "0060023","CD40 deficiency","omim","606843"
---
> "0060023","immunodeficiency with hyper IgM type 3","omim","606843"
> "0080560","congenital disorder of glycosylation Ih","omim","608104"
14798c29820
< "0110414","retinitis pigmentosa 3","omim","300029"
---
> "0080475","psoriasis 2","omim","602723"
14802c29824,29825
< "0110169","Charcot-Marie-Tooth disease axonal type 2P","omim","614436"
---
> "9955","hypoplastic left heart syndrome","omim","614435"
> "0050678","Blau syndrome","omim","186580"
14803a29827
> "0111414","trichohepatoenteric syndrome","omim","222470"
14805c29829
< "0060759","immunodeficiency with hyper IgM type 5","omim","608106"
---
> "0060474","familial erythrocytosis 2","omim","263400"
14808c29832,29833
< "0110644","long QT syndrome 1","omim","192500"
---
> "0060482","oculoauricular syndrome","omim","612109"
> "0111361","hypotrichosis-lymphedema-telangiectasia syndrome","omim","607823"
14810a29836,29837
> "0110252","cataract 37","omim","614422"
> "0111309","familial febrile seizures 6","omim","609253"
14814d29840
< "8158","complement component 5 deficiency","omim","609536"
14818c29844,29845
< "0060879","primary hypomagnesemia","omim","602014"
---
> "1612","breast cancer","omim","114480"
> "14778","blepharophimosis, ptosis, and epicanthus inversus syndrome","omim","110100"
14820c29847,29848
< "891","progressive myoclonus epilepsy","omim","254900"
---
> "12117","pulmonary alveolar microlithiasis","omim","265100"
> "0070082","schizophrenia 6","omim","603013"
14823c29851,29852
< "5557","testicular germ cell cancer","omim","300228"
---
> "9719","neovascular inflammatory vitreoretinopathy","omim","193235"
> "12638","hypertrophic pyloric stenosis","omim","612525"
14826a29856
> "14687","diastrophic dysplasia","omim","222600"
14828,14829c29858,29860
< "0111022","cone-rod dystrophy 16","omim","614500"
< "0110864","congenital stationary night blindness 1F","omim","615058"
---
> "0080569","congenital disorder of glycosylation Ir","omim","614507"
> "4028","angioma serpiginosum","omim","300652"
> "0060193","amyotrophic lateral sclerosis type 1","omim","105400"
14830a29862
> "13945","CADASIL","omim","125310"
14834d29865
< "0110488","autosomal recessive nonsyndromic deafness 3","omim","600316"
14835a29867
> "0080052","acromesomelic dysplasia, Grebe type","omim","200700"
14837,14839c29869,29872
< "9074","systemic lupus erythematosus","omim","614420"
< "0111105","maturity-onset diabetes of the young type 8","omim","609812"
< "11156","anhidrosis","omim","206600"
---
> "1657","ventricular septal defect","omim","614429"
> "0050873","follicular lymphoma","omim","151430"
> "0060229","Baraitser-Winter syndrome","omim","614583"
> "0080109","infantile myofibromatosis","omim","228550"
14847c29880,29882
< "10017","multiple endocrine neoplasia type 1","omim","131100"
---
> "10923","sickle cell anemia","omim","603903"
> "11634","myxedema","omim","255900"
> "0110890","inflammatory bowel disease 19","omim","612278"
14848a29884
> "0111564","hypoplastic or aplastic tibia with polydactyly","omim","188740"
14850a29887,29888
> "3081","cystic lymphangioma","omim","257350"
> "12185","otosclerosis","omim","615589"
14851a29890
> "14116","multiple symmetric lipomatosis","omim","151800"
14853,14854c29892,29896
< "9563","bronchiectasis","omim","613071"
< "0070236","Loeys-Dietz syndrome 5","omim","615582"
---
> "3138","acanthosis nigricans","omim","100600"
> "14219","renal tubular acidosis","omim","602722"
> "0060411","chromosome 1q21.1 deletion syndrome","omim","612474"
> "0060435","chromosome 1q21.1 duplication syndrome","omim","612475"
> "0050776","non-syndromic X-linked intellectual disability","omim","300912"
14856,14858c29898,29900
< "0050690","brachyolmia","omim","613678"
< "0110574","autosomal dominant nonsyndromic deafness 4B","omim","614614"
< "0060365","mandibulofacial dysostosis with alopecia","omim","616367"
---
> "0060384","acrofacial dysostosis, Catania type","omim","101805"
> "0080416","early infantile epileptic encephalopathy 32","omim","616366"
> "0110986","Joubert syndrome 17","omim","614615"
14862a29905
> "0060066","pyridoxine-responsive sideroblastic anemia","omim","206000"
14864,14866c29907,29912
< "2373","hereditary elliptocytosis","omim","611804"
< "0050763","ARC syndrome","omim","208085"
< "0110505","autosomal recessive nonsyndromic deafness 48","omim","609439"
---
> "0111496","combined oxidative phosphorylation deficiency 17","omim","615440"
> "10426","Klippel-Feil syndrome","omim","118100"
> "0110241","cataract 41","omim","116400"
> "0111364","Alzheimer's disease 9","omim","608907"
> "0060308","autosomal recessive non-syndromic intellectual disability","omim","614342"
> "0050645","arterial tortuosity syndrome","omim","208050"
14868c29914,29915
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","614343"
---
> "0050662","bestrophinopathy","omim","611809"
> "0090057","X-linked dystonia-parkinsonism","omim","314250"
14870a29918
> "0111121","nephronophthisis 13","omim","614377"
14872c29920
< "0060308","autosomal recessive non-syndromic intellectual disability","omim","614341"
---
> "0110876","holoprosencephaly 7","omim","610828"
14875c29923,29925
< "0111085","Fanconi anemia complementation group U","omim","617247"
---
> "5557","testicular germ cell cancer","omim","300228"
> "0080450","early infantile epileptic encephalopathy 17","omim","615473"
> "0080225","amyotrophic lateral sclerosis type 23","omim","617839"
14877,14878c29927,29931
< "0070113","Niemann-Pick disease type C1","omim","257220"
< "0110618","primary ciliary dyskinesia 13","omim","613193"
---
> "0111331","intellectual disability-severe speech delay-mild dysmorphism syndrome","omim","613670"
> "0080413","early infantile epileptic encephalopathy 18","omim","615476"
> "0050889","non-syndromic intellectual disability","omim","613192"
> "0050431","arrhythmogenic right ventricular cardiomyopathy","omim","107970"
> "0111495","combined oxidative phosphorylation deficiency 33","omim","617713"
14882a29936
> "0080256","Perrault syndrome 6","omim","617565"
14885,14886c29939,29942
< "0110522","autosomal recessive nonsyndromic deafness 71","omim","612789"
< "0110471","autosomal recessive nonsyndromic deafness 16","omim","603720"
---
> "3204","neurilemmomatosis","omim","615670"
> "0110089","asphyxiating thoracic dystrophy 5","omim","614376"
> "0080252","spastic ataxia 8","omim","617560"
> "0060422","chromosome 6pter-p24 deletion syndrome","omim","612582"
14892,14894c29948,29954
< "10923","sickle cell anemia","omim","603903"
< "0090132","complex cortical dysplasia with other brain malformations 7","omim","610031"
< "0110934","nemaline myopathy 7","omim","610687"
---
> "0110171","Charcot-Marie-Tooth disease axonal type 2S","omim","616155"
> "0070238","primary coenzyme Q10 deficiency 1","omim","607426"
> "12241","beta thalassemia","omim","603902"
> "0110823","hereditary spastic paraplegia 8","omim","603563"
> "0111208","distal hereditary motor neuronopathy type 2A","omim","158590"
> "0110083","arrhythmogenic right ventricular dysplasia 12","omim","611528"
> "0050877","pancreatic agenesis","omim","260370"
14896c29956
< "0110598","primary ciliary dyskinesia 14","omim","613807"
---
> "0080523","adult-onset leukoencephalopathy with axonal spheroids and pigmented glia","omim","221820"
14900a29961,29963
> "0110961","atypical Gaucher's disease due to saposin c deficiency","omim","610539"
> "0110915","childhood hypophosphatasia","omim","241510"
> "0110360","retinitis pigmentosa 39","omim","613809"
14903a29967,29968
> "12236","primary biliary cirrhosis","omim","109720"
> "0050587","trichotillomania","omim","613229"
14906c29971
< "14179","Bruton-type agammaglobulinemia","omim","300310"
---
> "3590","gestational trophoblastic neoplasm","omim","231090"
14909c29974,29977
< "0070078","schizophrenia 2","omim","603342"
---
> "0080286","spinocerebellar ataxia 44","omim","617691"
> "0080497","ovarian dysgenesis 5","omim","617690"
> "0111557","Charcot-Marie-Tooth disease type 2A2B","omim","617087"
> "4535","hypotrichosis","omim","605389"
14911c29979,29980
< "0070002","3-methylglutaconic aciduria type IX","omim","617698"
---
> "14793","hypohidrotic ectodermal dysplasia","omim","129490"
> "0070002","3-methylglutaconic aciduria type 9","omim","617698"
14912a29982,29983
> "8712","neurofibromatosis","omim","162260"
> "0111252","neurofibromatosis 2","omim","101000"
14914,14916c29985,29986
< "2583","agammaglobulinemia","omim","601495"
< "10608","celiac disease","omim","611598"
< "3315","lipoma","omim","151900"
---
> "9164","achalasia","omim","200400"
> "0050949","autosomal recessive hypophosphatemic rickets","omim","613312"
14918c29988
< "0110212","Charcot-Marie-Tooth disease X-linked recessive 4","omim","310490"
---
> "0110344","osteogenesis imperfecta type 5","omim","610967"
14921c29991
< "0110509","autosomal recessive nonsyndromic deafness 53","omim","609706"
---
> "0050576","Senior-Loken syndrome","omim","609254"
14923,14924c29993,29995
< "14723","beta-ketothiolase deficiency","omim","203750"
< "1339","Diamond-Blackfan anemia","omim","105650"
---
> "10772","thrombotic thrombocytopenic purpura","omim","274150"
> "758","situs inversus","omim","270100"
> "0070172","spermatogenic failure 15","omim","616950"
14925a29997
> "0111056","platelet-type bleeding disorder 3","omim","177820"
14927,14929c29999,30002
< "0110162","Charcot-Marie-Tooth disease, axonal type 2W","omim","616625"
< "2211","factor XIII deficiency","omim","613235"
< "1339","Diamond-Blackfan anemia","omim","610629"
---
> "0060169","benign familial infantile epilepsy","omim","605751"
> "0080573","congenital disorder of glycosylation Ix","omim","615597"
> "0080361","trimethylaminuria","omim","602079"
> "0090077","hypogonadotropic hypogonadism 4 with or without anosmia","omim","610628"
14932c30005
< "0060742","methylmalonic acidemia cblA type","omim","251100"
---
> "585","nephrolithiasis","omim","167030"
14935c30008
< "332","amyotrophic lateral sclerosis","omim","105400"
---
> "12177","common variable immunodeficiency","omim","607594"
14939,14941c30012,30021
< "1062","Fanconi syndrome","omim","134600"
< "0050780","Opitz-GBBB syndrome","omim","300000"
< "0070209","hereditary lymphedema ID","omim","615907"
---
> "13270","erythropoietic protoporphyria","omim","300752"
> "0060062","familial juvenile hyperuricemic nephropathy","omim","162000"
> "0111290","psoriasis 6","omim","605364"
> "0080500","ovarian dysgenesis 8","omim","618187"
> "0110440","dilated cardiomyopathy 1J","omim","605362"
> "14004","thoracic aortic aneurysm","omim","611788"
> "0050964","spinocerebellar ataxia type 14","omim","605361"
> "0080383","nephrotic syndrome type 4","omim","256370"
> "0111422","familial lipase maturation factor 1 deficiency","omim","246650"
> "3659","sialuria","omim","604369"
14944,14945c30024,30025
< "14118","familial lipoprotein lipase deficiency","omim","118830"
< "1339","Diamond-Blackfan anemia","omim","615909"
---
> "0111419","familial chylomicronemia due to inhibition of lipoprotein lipase activity","omim","118830"
> "0070204","familial partial lipodystrophy type 3","omim","604367"
14947c30027,30029
< "0070073","autosomal dominant non-syndromic intellectual disability 43","omim","616977"
---
> "0050565","autosomal recessive nonsyndromic deafness","omim","220290"
> "0110907","inflammatory bowel disease 6","omim","606674"
> "0060392","chromosome 14q11-q22 deletion syndrome","omim","613457"
14949,14951c30031,30032
< "0110536","autosomal recessive nonsyndromic deafness 91","omim","613453"
< "0110351","osteogenesis imperfecta type 11","omim","610968"
< "0060063","sideroblastic anemia 1","omim","300751"
---
> "0060287","cornea plana","omim","121400"
> "0060650","dicarboxylic aminoaciduria","omim","222730"
14954a30036
> "0111282","psoriasis 5","omim","604316"
14956a30039
> "0080137","multiple endocrine neoplasia type 4","omim","610755"
14958c30041,30043
< "8955","sideroblastic anemia","omim","300751"
---
> "6419","tetralogy of Fallot","omim","187500"
> "0080535","hypermanganesemia with dystonia","omim","613280"
> "0080507","Cornelia de Lange syndrome 3","omim","610759"
14961,14963c30046,30050
< "0050568","spondylocostal dysostosis","omim","608681"
< "0060468","Holt-Oram syndrome","omim","142900"
< "0110080","Leber congenital amaurosis 12","omim","610612"
---
> "0090100","ocular albinism with sensorineural deafness","omim","103470"
> "0110859","polycystic kidney disease 2","omim","613095"
> "12120","pulmonary alveolar proteinosis","omim","265120"
> "0050974","spinocerebellar ataxia type 25","omim","608703"
> "0090061","familial cold autoinflammatory syndrome","omim","120100"
14968c30055,30056
< "0060169","benign familial infantile epilepsy","omim","601764"
---
> "0060900","Parkinson's disease 14","omim","612953"
> "0050425","restless legs syndrome","omim","102300"
14970c30058
< "2340","craniosynostosis","omim","600593"
---
> "0050650","familial atrial fibrillation","omim","613980"
14972a30061
> "12241","beta thalassemia","omim","613985"
14975c30064
< "0070224","progressive familial intrahepatic cholestasis 4","omim","615878"
---
> "9406","hypopituitarism","omim","613986"
14977c30066
< "0070019","autosomal recessive dyskeratosis congenita 3","omim","613988"
---
> "0050711","aceruloplasminemia","omim","604290"
14980a30070,30071
> "0080429","early infantile epileptic encephalopathy 24","omim","615871"
> "14557","primary pulmonary hypertension","omim","265400"
14983c30074
< "0060331","mitochondrial complex V (ATP synthase) deficiency nuclear type 2","omim","614052"
---
> "0060233","cardiofaciocutaneous syndrome","omim","115150"
14986c30077
< "0060258","reticulate acropigmentation of Kitamura","omim","615537"
---
> "12185","otosclerosis","omim","611571"
14987a30079
> "0050641","Rh deficiency syndrome","omim","268150"
14988a30081
> "0060453","Reis-Bucklers corneal dystrophy","omim","608470"
14991c30084
< "0050781","Ogden syndrome","omim","300855"
---
> "0110705","hypotrichosis 8","omim","278150"
14994,14996c30087,30090
< "0110370","retinitis pigmentosa 55","omim","613575"
< "0110480","autosomal recessive nonsyndromic deafness 22","omim","607039"
< "1040","chronic lymphocytic leukemia","omim","109543"
---
> "5520","head and neck squamous cell carcinoma","omim","275355"
> "11870","Pick's disease","omim","172700"
> "0050818","transcobalamin II deficiency","omim","275350"
> "0080595","hyper IgE recurrent infection syndrome 3","omim","618282"
14998d30091
< "2988","antiphospholipid syndrome","omim","107320"
15000,15001c30093,30095
< "0060773","cleft lip-palate-ectodermal dysplasia syndrome","omim","225060"
< "9146","visceral leishmaniasis","omim","611382"
---
> "0080081","nonsyndromic congenital nail disorder 3","omim","151600"
> "0050981","spinocerebellar ataxia type 34","omim","133190"
> "14004","thoracic aortic aneurysm","omim","615436"
15002a30097
> "0111488","combined oxidative phosphorylation deficiency 31","omim","617228"
15004c30099
< "11830","myopia","omim","255500"
---
> "0110864","congenital stationary night blindness 1F","omim","615058"
15008c30103
< "0060233","cardiofaciocutaneous syndrome","omim","615279"
---
> "0111462","cardiofaciocutaneous syndrome 3","omim","615279"
15012c30107,30109
< "0050629","Aicardi-Goutieres syndrome","omim","610181"
---
> "0050848","obstructive sleep apnea","omim","107650"
> "0090093","hypogonadotropic hypogonadism 21 with or without anosmia","omim","615271"
> "0090082","hypogonadotropic hypogonadism 20 with or without anosmia","omim","615270"
15016c30113
< "0110251","cataract 15 multiple types","omim","615274"
---
> "0050576","Senior-Loken syndrome","omim","610189"
15017a30115
> "0110340","osteogenesis imperfecta type 4","omim","166220"
15021,15023c30119,30122
< "0060368","autosomal recessive juvenile Parkinson's disease 2","omim","600116"
< "0060256","Dowling-Degos disease","omim","615327"
< "0110421","late-adult onset retinitis pigmentosa","omim","268025"
---
> "0060368","Parkinson's disease 2","omim","600116"
> "7004","ACTH-secreting pituitary adenoma","omim","219090"
> "0080071","pseudo-Hurler polydystrophy","omim","252605"
> "0070192","autosomal recessive chronic granulomatous disease cytochrome b-positive type I","omim","233700"
15025,15026c30124,30129
< "0111078","tibial muscular dystrophy","omim","600334"
< "12236","primary biliary cirrhosis","omim","109720"
---
> "0060755","familial temporal lobe epilepsy 2","omim","608096"
> "0080091","spheroid body myopathy","omim","182920"
> "9212","pityriasis rubra pilaris","omim","173200"
> "0050972","spinocerebellar ataxia type 21","omim","607454"
> "9274","hyperlysinemia","omim","238710"
> "0070308","rippling muscle disease 1","omim","600332"
15029c30132
< "0111079","birdshot chorioretinopathy","omim","605808"
---
> "9245","Alagille syndrome","omim","118450"
15031c30134
< "0060824","syndromic X-linked intellectual disability Raymond type","omim","300799"
---
> "0050969","spinocerebellar ataxia type 18","omim","607458"
15036c30139,30140
< "0110252","cataract 37","omim","614422"
---
> "0111337","Jackson-Weiss syndrome","omim","123150"
> "0080358","fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2","omim","615119"
15038c30142
< "10283","prostate cancer","omim","611100"
---
> "9074","systemic lupus erythematosus","omim","614420"
15039a30144
> "13636","Fanconi anemia","omim","227650"
15045a30151
> "0111432","essential tremor 5","omim","616736"
15048c30154
< "0110098","atopic dermatitis 2","omim","605803"
---
> "0110194","Charcot-Marie-Tooth disease type 4B3","omim","615284"
15050d30155
< "0080037","Worth's syndrome","omim","607636"
15052c30157,30159
< "0050646","distal arthrogryposis","omim","178110"
---
> "0110506","autosomal recessive nonsyndromic deafness 49","omim","610153"
> "0080110","multiple pterygium syndrome","omim","178110"
> "0090034","myoclonic dystonia 11","omim","159900"
15053a30161
> "1588","thrombocytopenia","omim","273900"
15055c30163
< "11555","Fuchs' endothelial dystrophy","omim","610158"
---
> "0060352","Kleefstra syndrome","omim","610253"
15056a30165
> "0111284","psoriasis 9","omim","607857"
15058c30167
< "0110344","osteogenesis imperfecta type 5","omim","610967"
---
> "0110212","Charcot-Marie-Tooth disease X-linked recessive 4","omim","310490"
15060a30170
> "2231","factor XII deficiency","omim","234000"
15062c30172
< "0110907","inflammatory bowel disease 6","omim","606674"
---
> "0110723","neuronal ceroid lipofuscinosis 8","omim","600143"
15064c30174,30177
< "4990","essential tremor","omim","611456"
---
> "0111347","epidermolysis bullosa with congenital localized absence of skin and deformity of nails","omim","132000"
> "0111569","autosomal dominant vitreoretinochoroidopathy","omim","193220"
> "0090084","hypogonadotropic hypogonadism 5 with or without anosmia","omim","612370"
> "8955","sideroblastic anemia","omim","300751"
15066c30179,30180
< "10629","microphthalmia","omim","206900"
---
> "1882","atrial heart septal defect","omim","108800"
> "0060773","cleft lip-palate-ectodermal dysplasia syndrome","omim","225060"
15068a30183,30184
> "1024","leprosy","omim","609888"
> "12305","Bloch-Sulzberger syndrome","omim","308300"
15070c30186
< "0110343","osteogenesis imperfecta type 14","omim","615066"
---
> "0060336","3-methylglutaconic aciduria","omim","250950"
15072a30189
> "0080021","Schmid metaphyseal chondrodysplasia","omim","156500"