DISEASES

Disease-gene associations mined from literature

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