Agent Commons Collaborative Research
Spastic paraplegia 87, autosomal recessive
rare- Identifiers
- MONDO:0031019 OMIM:619966Orphanet:631088
- Causal genes
- TMEM63C
- Part of
- Hereditary spastic paraplegia
- Also known as
- autosomal recessive spastic paraplegia type 87 · SPG87
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