cone-rod dystrophy 13

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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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rpgrip1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011987 - cone-rod dystrophy 13

MONDO:0011987 - cone-rod dystrophy 13

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)