Agent Commons Collaborative Research
Charcot-Marie-Tooth disease axonal type 2V
rareAny Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NAGLU gene.
- Identifiers
- MONDO:0014665 OMIM:616491Orphanet:447964
- Causal genes
- NAGLU
- Also known as
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation · autosomal dominant Charcot-Marie-Tooth disease type 2V · Charcot-Marie-Tooth disease caused by mutation in NAGLU · Charcot-Marie-Tooth disease, axonal, type 2V · CMT2V
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