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Erythromelalgia

1 associated gene
11 signs/symptoms

COMMON GENES: 1

Channelopathy-associated congenital insensitivity to pain

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

Erythromelalgia

Channelopathy-associated congenital insensitivity to pain

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


COMMON GENES	SCN9A

Citations in the biomedical literature:

Erythromelalgia		Channelopathy-associated congenital insensitivity to pain

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare skin 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: unknown Average age onset: childhood Average age of death: no data available 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: No OMIM references 1 MeSH reference: D004916		External references: 1 OMIM reference - 2 MeSH references: D000699 / D009477

Erythromelalgia
	Very frequent - Autosomal dominant inheritance - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Peripheral neuropathy Frequent - Pruritus / itching Occasional - Acute ischemia of the lower limbs - Acute ischemic syndrome - Hypothermia - Myeloproliferative syndrome / chronic leukemia - Platelet disorders / thrombopathies - Repeat respiratory infections - Vascularitis / vasculitides / arteritis
Channelopathy-associated congenital insensitivity to pain
(no data available)