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Sodium channelopathy-related small fiber neuropathy
2 OMIM references -
2 associated genes
9 connected diseases
No signs/symptoms info
Disease Type of connection
Channelopathy-associated congenital insensitivity to pain
Paroxysmal extreme pain disorder
Primary erythermalgia
Dravet syndrome
Erythromelalgia
Generalized epilepsy with febrile seizures-plus context
Hereditary sensory and autonomic neuropathy type 2
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
SCN10A Q9Y5Y9604427
SCN9A Q15858603415
No signs/symptoms info available.