albinism, oculocutaneous

Preferred Label : albinism, oculocutaneous;

UMLS semantic type : T019 - Congenital Abnormality;

Origin ID

M0024616;

UMLS CUI

C0078918;

Automatic exact mappings (from CISMeF team)
- Albinism [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Oculocutaneous Albinism [NCIt concept]
- Oculocutaneous albinism [PASCAL descriptor]
- Oculocutaneous albinism [ICD-11 Sub-sub category]
- Oculocutaneous albinism [OMIM phenotypic series]
- Oculocutaneous albinism [ORDO Disease]
- Oculocutaneous albinism (disorder) [SNOMED CT concept]
- albinismus totalis [Disease (Nov.)]
- oculocutaneous albinism [DO Concept]
- oculocutaneous albinism, nos [SNOMED Notion]
MeSH narrower concept(s)
- albinism, Tyrosinase-Negative [MeSH concept]
- albinism, Tyrosinase-Positive [MeSH concept]
- albinism, Yellow-Mutant [MeSH concept]
Related record
- albinism, oculocutaneous [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Oculocutaneous Albinism [NCIt concept]
- Oculocutaneous albinism [ORDO Disease]
- Oculocutaneous albinism [PASCAL descriptor]
- Oculocutaneous albinism (disorder) [SNOMED CT concept]
- albinismus totalis [Disease (Nov.)]
- oculocutaneous albinism [DO Concept]
- oculocutaneous albinism, nos [SNOMED Notion]