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Summary Literature (0)
DOID:0081023 - retinal cone dystrophy 4

Disease Ontology Definition:A cone dystrophy that has_material_basis_in homozygous mutation in the CACNA2D4 gene on chromosome 12p13.

Synonyms:

Xenbase Genes : cacna2d4



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): cone dystrophy (is_a)