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Summary Literature (0)
DOID:0110005 - Leber congenital amaurosis 9

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36.

Synonyms: LCA9

Xenbase Genes : nmnat1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012056 - Leber congenital amaurosis 9


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

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