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Congenital bilateral absence of vas deferens
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital bilateral absence of vas deferens
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

CFTR
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CFTR
(0.63)
LMNA


Citations in the biomedical literature:


Congenital bilateral absence of vas deferens
CFTR
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



Congenital bilateral absence of vas deferens
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Synonym(s):
- Congenital bilateral agenesis of vas deferens
- Congenital bilateral aplasia of vas deferens
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare infertility
- Rare urogenital disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C535984
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.