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Late-onset autosomal recessive medullary cystic kidney disease
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital bilateral absence of vas deferens
1 OMIM reference -
1 associated gene
No signs/symptoms info
Late-onset autosomal recessive medullary cystic kidney disease
Congenital bilateral absence of vas deferens

FAN1
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
NPHP3
(UniProt - OMIM)
XPNPEP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
XPNPEP3
(0.72)
CFTR


Citations in the biomedical literature:


Late-onset autosomal recessive medullary cystic kidney disease
FAN1 NPHP3 XPNPEP3
Congenital bilateral absence of vas deferens
CFTR



Late-onset autosomal recessive medullary cystic kidney disease
Congenital bilateral absence of vas deferens

Synonym(s):
(no synonyms)

Synonym(s):
- Congenital bilateral agenesis of vas deferens
- Congenital bilateral aplasia of vas deferens
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare infertility
- Rare urogenital disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
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.