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Hereditary sensory and autonomic neuropathy type 5
rareHereditary sensory and autonomic neuropathy, type 5 (HSAN5) is characterized by loss of pain perception and impaired temperature sensitivity, in the absence of any other major neurological anomalies.
- Identifiers
- MONDO:0012092 OMIM:608654Orphanet:64752
- Causal genes
- NGF
- Part of
- Congenital insensitivity to pain
- Also known as
- autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF · congenital insensitivity to pain and thermal analgesia · hereditary sensory and autonomic neuropathy type V · HSAN V · HSAN5
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