Hyperinsulinemic hypoglycemia, familial, 2
Also known as KCNJ11 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11, hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, hyperinsulinemic hypoglycemia, familial, type 2+9 more
KCNJ11 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11, hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, hyperinsulinemic hypoglycemia, familial, type 2, HHF2, hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia, hyperinsulinemic hypoglycemia familial 2, hyperinsulinemic hypoglycemia, persistent, hyperinsulinism, congenital, hyperinsulinism, familial, hyperinsulinism, neonatal, nesidioblastosis, persistent hyperinsulinemic hypoglycemia of infancy.
What's happening now
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.
KCNJ11 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11, hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, hyperinsulinemic hypoglycemia, familial, type 2, HHF2, hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia, hyperinsulinemic hypoglycemia familial 2, hyperinsulinemic hypoglycemia, persistent, hyperinsulinism, congenital, hyperinsulinism, familial, hyperinsulinism, neonatal, nesidioblastosis, 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.