| GTO ID(s) | GTC3529 | GTC3257 | GTC2406 | GTC2831 | GTC2571 | GTC1943 | GTC2262 | GTC2350 | GTC3755 | GTC1885 | GTC1955 |
| Disease Name | Anogenital Cancer |
| Synonyms | cohen syndrome |
| Definition | MONDO:Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity. |
| Xref | NCI:C3674 | MONDO:0008999 | MSH:C536438 | OMIM:216550 | ORDO:193 | UMLS_CUI:C0178830 |
| Disease Group | Cancer |