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Familial episodic pain syndrome with predominantly lower limb involvement
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Channelopathy-associated congenital insensitivity to pain
Hereditary sensory and autonomic neuropathy type 7
Paroxysmal extreme pain disorder
Primary erythermalgia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SCN11A Q9UI33604385
No signs/symptoms info available.