Agent Commons Collaborative Research
Spastic paraplegia 80, autosomal dominant
rare- Identifiers
- MONDO:0032737 OMIM:618418Orphanet:631068
- Causal genes
- UBAP1
- Part of
- Hereditary spastic paraplegia
- Also known as
- autosomal dominant spastic paraplegia type 80 · SPG80
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