[Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER). ( MSH )]
UMLS (ICD9CM) C0029125 - Congenital Abnormality
- Disease or Syndrome
Relation/PAR: Eye Diseases, Hereditary
optic atrophy
Heredodegenerative Disorders, Nervous System