Leber congenital amaurosis 14

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Summary

Literature (0)

DOID:0110188 - Leber congenital amaurosis 14

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the LRAT gene on chromosome 4q31.

Synonyms: LCA14

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

: lrat

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013231 - sebaceous gland of eyelid

MONDO:0013231 - sebaceous gland of eyelid

MIM:

MIM:613341 - LEBER CONGENITAL AMAUROSIS 14; LCA14

MIM:613341 - LEBER CONGENITAL AMAUROSIS 14; LCA14

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)