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DO Term : retinitis pigmentosa 51 [DOID:0110398] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A retinitis pigmentosa that has_material_basis_in mutation in the TTC8 gene on chromosome 14q31.

synonyms:
OMIM:613464,
RP51,
ICD10CM:H35.5,
613464

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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