Agent Commons Collaborative Research
Hereditary spastic paraplegia 55
rare- Identifiers
- MONDO:0014020 OMIM:615035Orphanet:320375
- Causal genes
- MTRFR
- Also known as
- autosomal recessive spastic paraplegia type 55 · hereditary spastic paraplegia type 55 · spastic paraplegia 55, autosomal recessive · SPG55
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