Congenital insensitivity to pain-hypohidrosis syndrome
MONDO:0014662A 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.
Also known as: CIP-hypohidrosis syndrome, HSAN8, hereditary sensory and autonomic neuropathy type 8, hereditary sensory and autonomic neuropathy type VIII, HSAN 8, neuropathy, hereditary sensory and autonomic, type 8, neuropathy, hereditary sensory and autonomic, type VIII
7 clinical trials for this condition and its sub-types.
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Disease
(618)
Nervous system disorder
(217)
Hereditary disease
(172)
Peripheral nervous system disorder
(107)
Neuromuscular disease
(98)
Peripheral neuropathy
(90)
Hereditary sensory and autonomic neuropathy
(42)
Human disease
(14)
Hereditary peripheral neuropathy
(6)
Hereditary neurological disease
(5)