cone-rod dystrophy 10

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Summary

Literature (0)

DOID:0111017 - cone-rod dystrophy 10

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22.

Synonyms: CORD10

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

: sema4a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012464 - cone-rod dystrophy 10

MONDO:0012464 - cone-rod dystrophy 10

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)