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Renal tubular dysgenesis of genetic origin
1 OMIM reference -
4 associated genes
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
Renal tubular dysgenesis of genetic origin
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

ACE
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)
AGT
(UniProt - OMIM)
AGTR1
(UniProt - OMIM)
REN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACE
(0.49)
LMNA


Citations in the biomedical literature:


Renal tubular dysgenesis of genetic origin
ACE AGT AGTR1 REN
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



Renal tubular dysgenesis of genetic origin
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.