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Charcot-Marie-Tooth disease axonal type 2X
rareAny Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the SPG11 gene.
- Identifiers
- MONDO:0014726 OMIM:616668Orphanet:466775
- Causal genes
- SPG11
- Also known as
- ARCMT2X · autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation · Charcot-Marie-Tooth disease caused by mutation in SPG11 · Charcot-Marie-Tooth disease, axonal, type 2x · CMT2X
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