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DO Term : retinal cone dystrophy 1 [DOID:0081024] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cone dystrophy that is characterized as autosomal dominant form of diffuse cone degeneration.

synonyms:
MESH:C566719,
GARD:3196,
OMIM:180020,
180020

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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