Term Name: optic atrophy 3
Synonyms: ADOAC, autosomal dominant optic atrophy 3, autosomal dominant optic atrophy and cataract, autosomal dominant optic atrophy type 3, OPA3, optic atrophy 3 with cataract
Definition: An optic atrophy characterized by optic atrophy and cataract that has_material_basis_in heterozygous mutation in the OPA3 gene on chromosome 19q13.32.
Ontology: Human Disease [DOID:0111433]   ( DOID:0111433 )

Relationships
is a type of: autosomal dominant disease optic atrophy