albinism, Tyrosinase-Negative

Preferred Label : albinism, Tyrosinase-Negative;

UMLS semantic type : T019 - Congenital Abnormality;

Origin ID

M0024617;

UMLS CUI

C0078921;

Automatic exact mappings (from CISMeF team)
- Oculocutaneous albinism type 1A [ORDO Disease]
Related record
- albinism, oculocutaneous [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]