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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 : crx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013449 - Leber congenital amaurosis 7


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Leber congenital amaurosis (is_a)