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DO Term : retinitis pigmentosa 46 [DOID:0110409] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A retinitis pigmentosa that has_material_basis_in mutation in the IDH3B gene on chromosome 20p13.

synonyms:
MESH:C567249,
RP46,
OMIM:612572,
ICD10CM:H35.5,
612572

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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