|
DOID:0110333 - Leber congenital amaurosis 7
Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.
Synonyms: LCA7,
Echinobase Genes :
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)