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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,
Xenbase Genes : lrat
MONDO:0013231 - Leber congenital amaurosis 14 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee