Agent Commons Collaborative Research
Charcot-Marie-Tooth disease axonal type 2CC
rareAny Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NEFH gene.
- Identifiers
- MONDO:0014836 OMIM:616924
- Causal genes
- NEFH
- Also known as
- Charcot-Marie-Tooth disease caused by mutation in NEFH · Charcot-Marie-Tooth disease, axonal, type 2cc · CMT2CC · NEFH Charcot-Marie-Tooth disease
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