Charcot-Marie-Tooth disease type 1B (Q9190340)
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Charcot-Marie-Tooth disease type 1 that has material basis in heterozygous mutation in the gene encoding myelin protein zero (MPZ)
- CMT1B
- Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy
- Charcot-Marie-Tooth neuropathy type 1B
- HMSN IB
- HMSN1B
- autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B
- hereditary motor and sensory neuropathy IB
- peroneal muscular atrophy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Charcot-Marie-Tooth disease type 1B |
Charcot-Marie-Tooth disease type 1 that has material basis in heterozygous mutation in the gene encoding myelin protein zero (MPZ) |
|
Statements
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C118782
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Identifiers
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1 reference