Term Name: optic atrophy 6
Synonyms: OPA6
Definition: 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.
Ontology: Human Disease [DOID:0111435]   ( DOID:0111435 )

Relationships
is a type of: autosomal recessive disease optic atrophy