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Autosomal dominant Charcot-Marie-Tooth disease type 2W
rareAny Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the HARS gene.
- Identifiers
- MONDO:0014711 OMIM:616625Orphanet:488333
- Causal genes
- HARS1
- Also known as
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation · Charcot-Marie-Tooth disease type 2 caused by mutation in HARS · Charcot-Marie-Tooth disease, axonal, type 2w · CMT2W · HARS Charcot-Marie-Tooth disease type 2
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