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DO Term : oculocutaneous albinism type II [DOID:0070096] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA2 gene on chromosome 15q12-q13.

synonyms:
GARD:4038,
Oculocutaneous Albinism, Tyrosinase-Positive,
203200,
OCA2,
MESH:C537730,
OMIM:203200

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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