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"MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, type 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, susceptibility to, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "HPC3", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, type 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, susceptibility to, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "HPC4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, on chromosome 7", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, type 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "HPC5", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, type 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "HPC6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, susceptibility to", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "HPC7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer aggressiveness", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, type 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "HPC9", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "HPC10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene." }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "EHBP1 familial prostate cancer", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "familial prostate cancer caused by mutation in EHBP1", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, type 12", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "HPC12", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene." }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "MSMB familial prostate cancer", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "familial prostate cancer caused by mutation in MSMB", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, type 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "HPC13", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "HPC11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "HPC14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "HPC15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0700275", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0700275", "name": "prostate cancer, hereditary", "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents." }, { "id": "MIM:601518", "resource": "MIM", "url": "https://www.omim.org/entry/601518", "name": "Prostate cancer, hereditary, 1", "description": "Prostate cancer, hereditary, 1" }, { "id": "MIM:610997", "resource": "MIM", "url": "https://www.omim.org/entry/610997", "name": "Prostate cancer, hereditary, 9", "description": "Prostate cancer, hereditary, 9" }, { "id": "MIM:611868", "resource": "MIM", "url": "https://www.omim.org/entry/611868", "name": "Prostate cancer, hereditary, 12", "description": "Prostate cancer, hereditary, 12" }, { "id": "MIM:611928", "resource": "MIM", "url": "https://www.omim.org/entry/611928", "name": "Prostate cancer, hereditary, 13", "description": "Prostate cancer, hereditary, 13" }, { "id": "MIM:611955", "resource": "MIM", "url": "https://www.omim.org/entry/611955", "name": "Prostate cancer, hereditary, 11", "description": "Prostate cancer, hereditary, 11" }, { "id": "MIM:176807", "resource": "MIM", "url": "https://www.omim.org/entry/176807", "name": "Prostate cancer", "description": "Prostate cancer" } ], "unlinked_id_list": [], "evidence": [ { "id": "10283", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:10283" } ] }, { "disease_id": "DOID:2746", "recommended_name": { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "glycogen storage disease V", "description": "A glycogen storage disease that is characterized by onset of exercise intolerance and muscle cramps in childhood or adolescence and that has_material_basis_in homozygous or compound heterozygous mutation in the PYGM gene, which encodes muscle glycogen phosphorylase, on chromosome 11q13." }, "synonyms": [ { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "Glycogen storage disease, type V", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "McArdle's disease", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "glycogen storage disease type V", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "myophosphorylase deficiency", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "Glycogen storage disease 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease V", "description": "Myophosphorylase deficiency (McArdle's disease), or glycogen storage disease type 5 (GSD5), is a severe form of glycogen storage disease characterized by exercise intolerance." }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD due to muscle glycogen phosphorylase deficiency", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD type 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD type V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "McArdle disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "McArdle's disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "Mcardle disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "PYGM glycogen storage disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease caused by mutation in PYGM", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease type 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease type V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease, type V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogenosis due to muscle glycogen phosphorylase deficiency", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogenosis type 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogenosis type V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "myophosphorylase deficiency", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "McArdle type glycogen storage disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "Pygm deficiency", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease due to muscle glycogen phosphorylase deficiency", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "muscle glycogen phosphorylase deficiency", "description": "" }, { "id": "MIM:232600", "resource": "MIM", "url": "https://www.omim.org/entry/232600", "name": "Glycogen storage disease 5", "description": "Glycogen storage disease 5" } ], "unlinked_id_list": [], "evidence": [ { "id": "2746", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:2746" }, { "id": "2746", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:2746" } ] }, { "disease_id": "DOID:2746", "recommended_name": { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "glycogen storage disease V", "description": "A glycogen storage disease that is characterized by onset of exercise intolerance and muscle cramps in childhood or adolescence and that has_material_basis_in homozygous or compound heterozygous mutation in the PYGM gene, which encodes muscle glycogen phosphorylase, on chromosome 11q13." }, "synonyms": [ { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "Glycogen storage disease, type V", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "McArdle's disease", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "glycogen storage disease type V", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "myophosphorylase deficiency", "description": "" }, { "id": "DOID:2746", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2746", "name": "Glycogen storage disease 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease V", "description": "Myophosphorylase deficiency (McArdle's disease), or glycogen storage disease type 5 (GSD5), is a severe form of glycogen storage disease characterized by exercise intolerance." }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD due to muscle glycogen phosphorylase deficiency", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD type 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "GSD type V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "McArdle disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "McArdle's disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "Mcardle disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "PYGM glycogen storage disease", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease caused by mutation in PYGM", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease type 5", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease type V", "description": "" }, { "id": "MONDO:0009293", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009293", "name": "glycogen storage disease, type V", 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