Human genes for optic atrophy 6
Optic atrophy 6 [DOID:0111435]
An optic atrophy characterized by early onset of slowly progressive isolated optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 8q21-q22.
Synonyms: optic atrophy 6, DOID:0111435, OPA6