ODCs

Cytoscape Web

Click node...

Paroxysmal extreme pain disorder

1 OMIM reference -
3 associated genes
2 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 1

Erythromelalgia

1 associated gene
11 signs/symptoms

Paroxysmal extreme pain disorder

Erythromelalgia

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


COMMON GENES	SCN9A

Citations in the biomedical literature:

Paroxysmal extreme pain disorder		Erythromelalgia
	Synonym(s): - Familial rectal pain		Synonym(s): (no synonyms)

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: D004916


COMMON SIGNS	- Autosomal dominant inheritance

Paroxysmal extreme pain disorder		Erythromelalgia
	Frequent - Constipation		Very frequent - 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