Charcot-Marie-Tooth disease type 6 (Q21124580)
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Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity
- hereditary motor and sensory neuropathy type 6
- HMSN6A
- NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA
- Charcot-Marie-Tooth Disease, Type 6A
- Peripheral Neuropathy and Optic Atrophy
- Hmsn 6A
- Neuropathy, Hereditary Motor and Sensory, Type 6
- Charcot-Marie-Tooth Disease, Type 6
- NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA; HMSN6A
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Charcot-Marie-Tooth disease type 6 |
Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity |
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