ODCs

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1 OMIM reference -
3 associated genes
2 signs/symptoms

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Paroxysmal extreme pain disorder

Familial episodic pain syndrome with predominantly lower limb involvement

Citations in the biomedical literature:

Paroxysmal extreme pain disorder		Familial episodic pain syndrome with predominantly lower limb involvement
	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

	Classification (ICD10): (no data available)		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		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		External references: 1 OMIM reference - No MeSH references

Paroxysmal extreme pain disorder
	Very frequent - Autosomal dominant inheritance Frequent - Constipation
Familial episodic pain syndrome with predominantly lower limb involvement
(no data available)