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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 on chromosome 1p22.
Synonyms: CORD3
OMIM:604116 - CONE-ROD DYSTROPHY 3; CORD3 |
MONDO:0011395 - cone-rod dystrophy 3 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
cone-rod dystrophy (is_a)