C125388Level 6
Neuropathy, Hereditary Sensory and Autonomic, Type VII
**Semantic type:** Disease or Syndrome
**Definition:** A very rare disorder caused by mutation in the SCN11A gene. Affected individuals are unable to experience pain since birth resulting in self-inflicted injuries.
**Synonyms:** - HSAN7 - Hereditary Sensory and Autonomic Neuropathy Type VII
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