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"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:2750", "recommended_name": { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "glycogen storage disease IV", "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12." }, "synonyms": [ { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Amylopectinosis", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Branching-transferase deficiency glycogenosis", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Glycogen storage disease, type IV", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "brancher deficiency glycogenosis", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "deficiency of 1,4-alpha-glucan branching enzyme", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Glycogen storage disease 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease due to glycogen branching enzyme deficiency", "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases." }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Andersen Disease (GSD IV)", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Andersen disease", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Andersen's disease", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GBE1 glycogen storage disease", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD due to glycogen branching enzyme deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD type 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD type IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "amylopectinosis", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "brancher deficiency glycogenosis", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "branching-transferase deficiency glycogenosis", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "deficiency of 1,4-alpha-glucan branching enzyme", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease caused by mutation in GBE1", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease due to glycogen branching enzyme deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease type 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease type IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease, type IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogenosis due to glycogen branching enzyme deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogenosis type 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogenosis type IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, classic hepatic", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, neuromuscular form, adult, with isolated myopathy", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, neuromuscular form, childhood", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, neuromuscular form, congenital", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, neuromuscular form, fatal perinatal", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, nonprogressive hepatic", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Gbe1 deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "brancher deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "cirrhosis, familial, with deposition of abnormal glycogen", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen branching enzyme deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogenosis 4", "description": "" }, { "id": "MIM:232500", "resource": "MIM", "url": "https://www.omim.org/entry/232500", "name": "Glycogen storage disease 4", "description": "Glycogen storage disease 4" } ], "unlinked_id_list": [], "evidence": [ { "id": "232500", "database": "MIM", "url": "https://www.omim.org/entry/232500" }, { "id": "2750", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:2750" } ] }, { "disease_id": "DOID:2750", "recommended_name": { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "glycogen storage disease IV", "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12." }, "synonyms": [ { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Amylopectinosis", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Branching-transferase deficiency glycogenosis", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Glycogen storage disease, type IV", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "brancher deficiency glycogenosis", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "deficiency of 1,4-alpha-glucan branching enzyme", "description": "" }, { "id": "DOID:2750", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2750", "name": "Glycogen storage disease 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease due to glycogen branching enzyme deficiency", "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases." }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Andersen Disease (GSD IV)", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Andersen disease", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Andersen's disease", "description": "" }, { "id": "MONDO:0009292", 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"description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD IV, nonprogressive hepatic", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "GSD4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "Gbe1 deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "brancher deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "cirrhosis, familial, with deposition of abnormal glycogen", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen branching enzyme deficiency", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease 4", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogen storage disease IV", "description": "" }, { "id": "MONDO:0009292", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009292", "name": "glycogenosis 4", "description": "" }, { "id": "MIM:232500", "resource": "MIM", "url": "https://www.omim.org/entry/232500", "name": "Glycogen storage disease 4", "description": "Glycogen storage disease 4" } ], "unlinked_id_list": [], "evidence": [ { "id": "232500", "database": "MIM", "url": "https://www.omim.org/entry/232500" }, { "id": "2750", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:2750" } ] } ] } ] } }