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DO Term : oculocutaneous albinism type VI [DOID:0080614] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1.

synonyms:
OMIM:113750,
113750

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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