Hyperinsulinemic hypoglycemia, familial, 1
Also known as ABCC8 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8, hyperinsulinemic hypoglycemia due to SUR1 deficiency, hyperinsulinemic hypoglycemia, familial, type 1+7 more
ABCC8 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8, hyperinsulinemic hypoglycemia due to SUR1 deficiency, hyperinsulinemic hypoglycemia, familial, type 1, HHF1, Nesidioblastosis of pancreas, hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia, hyperinsulinism, congenital, hyperinsulinism, familial, with pancreatic Nesidioblastosis, hypoglycemia, hyperinsulinemic, of infancy, persistent hyperinsulinemic hypoglycemia of infancy.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
ABCC8 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8, hyperinsulinemic hypoglycemia due to SUR1 deficiency, hyperinsulinemic hypoglycemia, familial, type 1, HHF1, Nesidioblastosis of pancreas, hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia, hyperinsulinism, congenital, hyperinsulinism, familial, with pancreatic Nesidioblastosis, hypoglycemia, hyperinsulinemic, of infancy, persistent hyperinsulinemic hypoglycemia of infancy
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.