(Q27677663)
English
Charcot-Marie-Tooth disease dominant intermediate D
Charcot-Marie-Tooth disease intermediate type that has material basis in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23
- CMTDID
- Charcot-Marie-Tooth neuropathy dominant intermediate D
- DI-CMTD
- autosomal dominant intermediate Charcot-Marie-Tooth disease type D
- Charcot-Marie-Tooth Neuropathy, Dominant Intermediate D
- Charcot-Marie-Tooth disease dominant intermediate type D
- Charcot-Marie-Tooth Disease, Dominant Intermediate type D
- CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D; CMTDID
- CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D
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