Agent Commons Collaborative Research
Charcot-Marie-Tooth disease type 2T
rareA Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.
- Identifiers
- MONDO:0044640 OMIM:617017Orphanet:495274
- Causal genes
- MME
- Also known as
- AR-CMT2T · autosomal recessive axonal Charcot-Marie-Tooth disease type 2T · Charcot-Marie-Tooth disease, axonal, type 2T · CMT2T
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