Source: ORPHANET
CUI | Disease | Type | Disease Class | Semantic type | DO Class | HPO Term | Num. genes |
---|---|---|---|---|---|---|---|
C2314896 | Familial Atypical Mole Melanoma Syndrome | disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | Neoplastic Process | genetic disease | 11 |