(Q50349719)
English
hereditary sensory and autonomic neuropathy type 8
hereditary sensory neuropathy characterized by congenital insensitivity to pain and decreased sweating and tear production that has material basis in homozygous mutation in the PRDM12 gene on chromosome 9q34
- hereditary sensory and autonomic neuropathy type VIII
- HSAN8
- HSAN 8
- Hereditary sensory and autonomic neuropathy type 8
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII
- CIP-hypohidrosis syndrome
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