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Up to: Congenital nervous system disorder · Hereditary sensory and autonomic neuropathy
Congenital insensitivity to pain-hypohidrosis syndrome
A 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.
This condition has no sub-types.