hereditary sensory and autonomic neuropathy type 2A (Q50349721)
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hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has material basis in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13
- HSAN2A
- hereditary sensory and autonomic neuropathy type IIA
- Acroosteolysis, Giaccai Type
- Acroosteolysis, Neurogenic
- HSAN 2A
- Neuropathy, Congenital Sensory
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA; HSAN2A
- Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive
- HSN 2A
- Neuropathy, Progressive Sensory, of Children
- Morvan Disease
- Neuropathy, Hereditary Sensory, Type 2A
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary sensory and autonomic neuropathy type 2A |
hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has material basis in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13 |
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