Human genes for Leber congenital amaurosis 3
Leber congenital amaurosis 3 [DOID:0110331]
A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31.
Synonyms: Leber congenital amaurosis 3, DOID:0110331, LCA3