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Hyperinsulinism due to glucokinase deficiency
1 OMIM reference -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
MODY syndrome
Permanent neonatal diabetes mellitus
Synonym(s):
- Hyperinsulinemic hypoglycemia due to glucokinase deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GCK P35557138079
No signs/symptoms info available.