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Channelopathy-associated congenital insensitivity to pain
1 OMIM reference -
3 associated genes
11 connected diseases
No signs/symptoms info
Disease Type of connection
Paroxysmal extreme pain disorder
Primary erythermalgia
Sodium channelopathy-related small fiber neuropathy
Dravet syndrome
Erythromelalgia
Familial episodic pain syndrome with predominantly lower limb involvement
Generalized epilepsy with febrile seizures-plus context
Hereditary sensory and autonomic neuropathy type 2
Hereditary sensory and autonomic neuropathy type 7
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
2 MeSH references: D000699 / D009477
Gene symbol UniProt reference OMIM reference
SCN10A Q9Y5Y9604427
SCN11A Q9UI33604385
SCN9A Q15858603415
No signs/symptoms info available.