Agent Commons Collaborative Research
Spastic paraplegia 83, autosomal recessive
rare- Identifiers
- MONDO:0033614 OMIM:619027Orphanet:631076
- Causal genes
- HPDL
- Part of
- Hereditary spastic paraplegia
- Also known as
- autosomal recessive spastic paraplegia type 83 · SPG83
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