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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
Congenital bilateral absence of vas deferens
Idiopathic bronchiectasis

CFTR CFTR
SCNN1A
SCNN1B
SCNN1G


COMMON
GENES
CFTR



Citations in the biomedical literature:


Congenital bilateral absence of vas deferens
CFTR
Idiopathic bronchiectasis
SCNN1A SCNN1B SCNN1G



Congenital bilateral absence of vas deferens
Idiopathic bronchiectasis

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 respiratory disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the respiratory system -

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:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C535984
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.