An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss. [ NCI ]

Synonyms: Autosomal Dominant Optic Atrophy

This is just here as a test because I lose it

Term information

Subsets

NCIT_C165258

Contributing Source

Cellosaurus

Preferred Name

Autosomal Dominant Optic Atrophy

Semantic Type

Disease or Syndrome

UMLS CUI

C0338508

code

C84577