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Disease
autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Also known as autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, dominant KATP hyperinsulinism due to Kir6.2 deficiency.
12
Associated genes
1
Related proteins
What's happening now
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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.
Synonyms
autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, dominant KATP hyperinsulinism due to Kir6.2 deficiency
References & data sources
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.