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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,
Echinobase Genes :
MIM:613341 - leber congenital amaurosis 14; lca14 retinal dystrophy, early-onset severe, lrat-related, included;; retinitis pigmentosa, juvenile, lrat-related, included |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Leber congenital amaurosis (is_a)