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

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

Rare Disease

MONDO:0015003

Also Known As

DYTOABGdystonia, childhood-onset, with optic atrophy and basal ganglia abnormalitiesdystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities; DYTOABGdystonia 29, childhood-onset

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Associated Genes

MECR ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

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

Also Known As

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases