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Summary Literature (0)
DOID:0111011 - cone-rod dystrophy 6

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.

Synonyms: CORD6, RCD2, retinal cone dystrophy 2

Xenbase Genes : gucy2d

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011143 - upper urinary tract

MIM:
MIM:601777 - CONE-ROD DYSTROPHY 6; CORD6

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)