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Summary Literature (0)
DOID:0111010 - cone-rod dystrophy 5

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1.

Synonyms: CORD5,

Xenbase Genes : pitpnm3, gucy2d

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010969 - cone-rod dystrophy 5


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)