Leber congenital amaurosis 16

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Summary

Literature (0)

DOID:0110118 - Leber congenital amaurosis 16

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the KCNJ13 gene on chromosome 2q37.

Synonyms: LCA16

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

: kcnj13

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013613 - Leber congenital amaurosis 16

MONDO:0013613 - Leber congenital amaurosis 16

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)