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Familial progressive cardiac conduction defect

5 OMIM references -
4 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

Congenital analbuminemia

1 associated gene
No signs/symptoms info

Familial progressive cardiac conduction defect

Congenital analbuminemia

NKX2-5	(UniProt - OMIM)		ALB	(UniProt - OMIM)
SCN1B	(UniProt - OMIM)
SCN5A	(UniProt - OMIM)
TRPM4	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SCN5A	(0.72)	ALB

Citations in the biomedical literature:

Familial progressive cardiac conduction defect		Congenital analbuminemia
	Synonym(s): - Familial LenÃ¨gre disease - Familial Lev disease - Familial Lev-LenÃ¨gre disease - Familial PCCD - Familial progressive heart block - Hereditary bundle branch defect		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

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

Familial progressive cardiac conduction defect
	Frequent - Cardiac rhythm disorder / arrhythmia
Congenital analbuminemia
(no data available)