ODCs

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

PROTEIN INTERACTIONS: 1

5 OMIM references -
4 associated genes
1 sign/symptom

Congenital lethal myopathy, Compton-North type

Familial progressive cardiac conduction defect


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CNTN1	(0.72)	SCN1B

Citations in the biomedical literature:

Congenital lethal myopathy, Compton-North type		Familial progressive cardiac conduction defect
	Synonym(s): (no synonyms)		Synonym(s): - Familial LenÃ¨gre disease - Familial Lev disease - Familial Lev-LenÃ¨gre disease - Familial PCCD - Familial progressive heart block - Hereditary bundle branch defect

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

	Classification (ICD10): - Diseases of the nervous system -		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: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 5 OMIM references - No MeSH references

Familial progressive cardiac conduction defect
	Frequent - Cardiac rhythm disorder / arrhythmia
Congenital lethal myopathy, Compton-North type
(no data available)