X-linked cone-rod dystrophy 3

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Summary

Literature (0)

DOID:0111007 - X-linked cone-rod dystrophy 3

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.

Synonyms: CORDX3

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

: cacna1f

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010335 - maxillary process mesenchyme from head mesenchyme

MONDO:0010335 - maxillary process mesenchyme from head mesenchyme

MIM:

MIM:300476 - CONE-ROD DYSTROPHY, X-LINKED, 3; CORDX3

MIM:300476 - CONE-ROD DYSTROPHY, X-LINKED, 3; CORDX3

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), X-linked recessive disease (is_a)