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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
2 associated genes
1 sign/symptom
Hyperinsulinism due to HNF4A deficiency
Familial hypospadias

HNF4A AR
MAMLD1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HNF4A
(0.55)
AR



Citations in the biomedical literature:


Hyperinsulinism due to HNF4A deficiency
HNF4A
Familial hypospadias
AR MAMLD1



Hyperinsulinism due to HNF4A deficiency
Familial hypospadias

Synonym(s):
- Hyperinsulinemic hypoglycemia due to HNF4A deficiency

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references

Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Hyperinsulinism due to HNF4A deficiency

(no data available)