ODCs

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

COMMON GENES: 3

1 OMIM reference -
3 associated genes
2 signs/symptoms

Channelopathy-associated congenital insensitivity to pain

Paroxysmal extreme pain disorder

Citations in the biomedical literature:

Channelopathy-associated congenital insensitivity to pain		Paroxysmal extreme pain disorder
	Synonym(s): (no synonyms)		Synonym(s): - Familial rectal pain

	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

Paroxysmal extreme pain disorder
	Very frequent - Autosomal dominant inheritance Frequent - Constipation
Channelopathy-associated congenital insensitivity to pain
(no data available)