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Summary Literature (0)
DOID:0111019 - cone-rod dystrophy 12

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15.

Synonyms: CORD12

Xenbase Genes : prom1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012983 - cone-rod dystrophy 12


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)