Source: ORPHANET
CUI | Disease | Type | Disease Class | Semantic type | DO Class | HPO Term | Num. genes |
---|---|---|---|---|---|---|---|
C1833921 | Familial medullary thyroid carcinoma | disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases | Neoplastic Process | genetic disease; disease of anatomical entity; disease of cellular proliferation | 3 |