ODCs

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1 OMIM reference -
3 associated genes
No signs/symptoms info

COMMON GENES: 3

1 OMIM reference -
3 associated genes
No signs/symptoms info

Primary erythermalgia

Channelopathy-associated congenital insensitivity to pain

Citations in the biomedical literature:

Primary erythermalgia		Channelopathy-associated congenital insensitivity to pain

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		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 - No MeSH references		External references: 1 OMIM reference - 2 MeSH references: D000699 / D009477

No signs/symptoms info available.