Leber congenital amaurosis 3

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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

Echinobase 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

: spata7

MIM:

MIM:604232 - leber congenital amaurosis 3; lca3 retinitis pigmentosa, juvenile, spata7-related, included

MIM:604232 - leber congenital amaurosis 3; lca3 retinitis pigmentosa, juvenile, spata7-related, included

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)