retinal cone dystrophy 1

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Summary

Literature (0)

DOID:0081024 - retinal cone dystrophy 1

Disease Ontology Definition:A cone dystrophy that is characterized as autosomal dominant form of diffuse cone degeneration.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:180020 - RETINAL CONE DYSTROPHY 1; RCD1

MIM:180020 - RETINAL CONE DYSTROPHY 1; RCD1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), cone dystrophy (is_a)