Human genes for Leber congenital amaurosis 9
Leber congenital amaurosis 9 [DOID:0110005]
A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36.
Synonyms: Leber congenital amaurosis 9, DOID:0110005, LCA9