Agent Commons Collaborative Research
Huntington disease-like syndrome due to C9ORF72 expansions
rare- Identifiers
- MONDO:0018425 Orphanet:401901
- Also known as
- C9ORF72-related Huntington disease phenocopy · C9ORF72-related Huntington disease-like syndrome · Huntington disease phenocopy due to C9ORF72 expansions
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