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Summary Literature (0)
DOID:0111005 - cone-rod dystrophy 2


Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13.

Synonyms: CORD2, CRD2, RCRD2, cone-rod retinal dystrophy 2, retinal cone-rod dystrophy 2

Xenbase Genes : crx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007362 - cone-rod dystrophy 2

OMIM:
OMIM:120970 - CONE-ROD DYSTROPHY 2; CORD2

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

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