|
DOID:0110217 - Leber congenital amaurosis 17
Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the GDF6 gene on chromosome 8q22.
Synonyms: LCA17,
Echinobase Genes :
MIM:615360 - leber congenital amaurosis 17; lca17 |
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)