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Summary Literature (0)
DOID:0110331 - Leber congenital amaurosis 3

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31.

Synonyms: LCA3

Xenbase Genes : spata7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011415 - Leber congenital amaurosis 3

MIM:
MIM:604232 - LEBER CONGENITAL AMAUROSIS 3; LCA3

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)