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Summary Literature (1)
DOID:0111013 - cone-rod dystrophy 3

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ABCA4 gene on chromosome 1p22.

Synonyms: CORD3

Xenbase Genes : abca4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011395 - cone-rod dystrophy 3

MIM:
MIM:604116 - CONE-ROD DYSTROPHY 3; CORD3

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

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