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Congenital analbuminemia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial progressive cardiac conduction defect
5 OMIM references -
4 associated genes
1 sign/symptom
Congenital analbuminemia
Familial progressive cardiac conduction defect

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

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


Citations in the biomedical literature:


Congenital analbuminemia
ALB
Familial progressive cardiac conduction defect
NKX2-5 SCN1B SCN5A TRPM4



Congenital analbuminemia
Familial progressive cardiac conduction defect

Synonym(s):
(no synonyms)

Synonym(s):
- Familial Lenègre disease
- Familial Lev disease
- Familial Lev-Lenègre disease
- Familial PCCD
- Familial progressive heart block
- Hereditary bundle branch defect
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
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: normal
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:
No OMIM references
No MeSH references
External references:
5 OMIM references -
No MeSH references
Familial progressive cardiac conduction defect

Frequent
- Cardiac rhythm disorder / arrhythmia



Congenital analbuminemia

(no data available)