Leber congenital amaurosis 11

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Summary

Literature (0)

DOID:0110216 - Leber congenital amaurosis 11

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation n the IMPDH1 gene on chromosome 7q31.3-q32.

Synonyms: LCA11

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

: impdh1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013454 - Leber congenital amaurosis 11

MONDO:0013454 - Leber congenital amaurosis 11

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

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

Parent(s): autosomal dominant disease (is_a), Leber congenital amaurosis (is_a)