Leber congenital amaurosis 7

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Summary

Literature (0)

DOID:0110333 - Leber congenital amaurosis 7

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.

Synonyms: LCA7

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

: crx

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013449 - Leber congenital amaurosis 7

MONDO:0013449 - Leber congenital amaurosis 7

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Leber congenital amaurosis (is_a), monogenic disease (is_a)