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dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive neurologic disorder characterized by childhood-onset dystonia, basal ganglia degeneration and optic atrophy with decreased visual acuity. Dystonia is defined by the presence of sustained involuntary muscle contraction, often leading to abnormal postures. DYTOABG severity is variable, and some patients lose independent ambulation.
Mondo Term and Equivalent IDs
MONDO:0015003:  dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
Orphanet:508093: 
UMLS:C4310634: