brown oculocutaneous albinism

Preferred Label : brown oculocutaneous albinism;

MeSH note : PROM mutation in OCA2;

MeSH synonym : albinism, brown oculocutaneous;

Origin ID

C562662;

UMLS CUI

C0268497;

Automatic exact mappings (from CISMeF team)
- Albinism, oculocutaneous, type II [OMIM Phenotype]
- Brown oculocutaneous albinism [ICD-11 More detail]
- Brown oculocutaneous albinism (disorder) [SNOMED CT concept]
- Oculocutaneous albinism type 3 [ORDO Disease]
- brown oculocutaneous albinism [SNOMED Notion]
MeSH term(s) associated for indexing
- albinism, oculocutaneous [MeSH Descriptor]
Record concept(s)
- brown oculocutaneous albinism [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Brown oculocutaneous albinism (disorder) [SNOMED CT concept]
- brown oculocutaneous albinism [SNOMED Notion]