cone-rod dystrophy 11

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Summary

Literature (0)

DOID:0111018 - cone-rod dystrophy 11

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the RAX2 gene on chromosome 19p13.

Synonyms: CORD11

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

: rax2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012483 - serosa of cloaca

MONDO:0012483 - serosa of cloaca

MIM:

MIM:610381 - CONE-ROD DYSTROPHY 11; CORD11

MIM:610381 - CONE-ROD DYSTROPHY 11; CORD11

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)