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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Renal tubular dysgenesis of genetic origin

LMNA ACE
AGT
AGTR1
REN


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Renal tubular dysgenesis of genetic origin
ACE AGT AGTR1 REN



Laminopathy type Decaudain-Vigouroux
Renal tubular dysgenesis of genetic origin

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

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.