Leber congenital amaurosis 15

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Summary

Literature (0)

DOID:0110189 - Leber congenital amaurosis 15

Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3.

Synonyms: LCA15

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

: tulp1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013457 - Leber congenital amaurosis 15

MONDO:0013457 - Leber congenital amaurosis 15

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)