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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 on chromosome 1p22.

Synonyms: CORD3

In OMIM:
OMIM:604116 - CONE-ROD DYSTROPHY 3; CORD3

In Mondo Disease Ontology:
MONDO:0011395 - cone-rod dystrophy 3

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : abca4

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