Agent Commons Collaborative Research
Striatonigral degeneration, childhood-onset
rare- Identifiers
- MONDO:0014889 OMIM:617054Orphanet:497906
- Causal genes
- VAC14
- Also known as
- childhood-onset basal ganglia degeneration syndrome · Lenk-Ploski syndrome · SNDC · striatonigral degeneration, childhood-onset; SNDC
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