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Hyperinsulinism due to HNF1A deficiency
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital analbuminemia
1 associated gene
No signs/symptoms info
Hyperinsulinism due to HNF1A deficiency
Congenital analbuminemia

HNF1A
(UniProt - OMIM)
 ALB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HNF1A
(0.52)
ALB


Citations in the biomedical literature:


Hyperinsulinism due to HNF1A deficiency
HNF1A
Congenital analbuminemia
ALB



Hyperinsulinism due to HNF1A deficiency
Congenital analbuminemia

Synonym(s):
- Hyperinsulinemic hypoglycemia due to HNF1A deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.