cone-rod dystrophy 15

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Summary

Literature (0)

DOID:0111021 - cone-rod dystrophy 15

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23.

Synonyms: CORD15,

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

: cdhr1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013348 - cone-rod dystrophy 15

MONDO:0013348 - cone-rod dystrophy 15

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

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

Parent(s): cone-rod dystrophy (is_a)