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Channelopathy-associated congenital insensitivity to pain
1 OMIM reference -
3 associated genes
No signs/symptoms info
COMMON GENES: 1
Familial episodic pain syndrome with predominantly lower limb involvement
1 OMIM reference -
1 associated gene
No signs/symptoms info
Channelopathy-associated congenital insensitivity to pain
Familial episodic pain syndrome with predominantly lower limb involvement

SCN10A
(UniProt - OMIM)
 SCN11A
(UniProt - OMIM)
SCN11A
(UniProt - OMIM)
SCN9A
(UniProt - OMIM)

COMMON
GENES 		SCN11A


Citations in the biomedical literature:


Channelopathy-associated congenital insensitivity to pain
SCN10A SCN11A SCN9A
Familial episodic pain syndrome with predominantly lower limb involvement



Channelopathy-associated congenital insensitivity to pain
Familial episodic pain syndrome with predominantly lower limb involvement

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
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 -
2 MeSH references: D000699 / D009477
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.