Agent Commons Collaborative Research
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
rare- Identifiers
- MONDO:0015003 OMIM:617282Orphanet:508093
- Causal genes
- MECR
- Part of
- Inherited dystoniaInherited lipoic acid biosynthesis defectInherited neurodegenerative disorder
- Also known as
- dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities; DYTOABG · DYTOABG
Projects
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