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Single ventricular septal defect
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hyperinsulinism due to HNF4A deficiency
1 associated gene
No signs/symptoms info
Single ventricular septal defect
Hyperinsulinism due to HNF4A deficiency

CITED2
(UniProt - OMIM)
 HNF4A
(UniProt - OMIM)
GATA4
(UniProt - OMIM)
GATA5
(UniProt - OMIM)
NKX2-5
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CITED2
(0.7)
HNF4A


Citations in the biomedical literature:


Single ventricular septal defect
CITED2 GATA4 GATA5 NKX2-5
Hyperinsulinism due to HNF4A deficiency
HNF4A



Single ventricular septal defect
Hyperinsulinism due to HNF4A deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Hyperinsulinemic hypoglycemia due to HNF4A deficiency
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.