Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0111016 - cone-rod dystrophy 13


Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.2.

Synonyms: CORD13

In OMIM:
OMIM:608194 - CONE-ROD DYSTROPHY 13; CORD13

In Mondo Disease Ontology:
MONDO:0011987 - cone-rod dystrophy 13

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

Xenbase Genes : rpgrip1

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