You are using an outdated browser. Please upgrade your browser to improve your experience.

Leber optic atrophy and dystonia

Disease Summary
Associated Targets (4)
Tclin

4


GARD Rare
Uniprot Description Part of a spectrum of Leber hereditary optic neuropathy. It is characterized by the association of optic atrophy and central vision loss with dystonia.
Mondo Term and Equivalent IDs
MONDO:0010772:  Leber optic atrophy and dystonia
DOID:0111755: 
GARD:0008476: 
MESH:C536024: 
UMLS:C1839040: