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DO Term : retinitis pigmentosa 32 [DOID:0110355] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A retinitis pigmentosa that has_material_basis_inhomozygous mutation in the CLCC1 gene on chromosome 1p13.

synonyms:
RP32,
MESH:C563689,
ICD10CM:H35.5,
OMIM:609913,
609913

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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