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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Congenital bilateral absence of vas deferens

LMNA CFTR


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Congenital bilateral absence of vas deferens
CFTR



Laminopathy type Decaudain-Vigouroux
Congenital bilateral absence of vas deferens

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
- Congenital bilateral agenesis of vas deferens
- Congenital bilateral aplasia of vas deferens

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare infertility
- Rare urogenital disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(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

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

No signs/symptoms info available.