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FHH - familial hyperinsulinemic hypoglycemia
disorderSNOMED 1296480005CUI C5848294
Overview
FHH - familial hyperinsulinemic hypoglycemia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Persistent hyperinsulinemic hypoglycemia of infancy(child)
Hyperinsulinism due to insulin receptor deficiency(child)
Adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia(child)
Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome(child)
Genetic disease(parent)
Hyperinsulinism(parent)
Familial disease(parent)
Hypoglycaemic syndrome(parent)
Quick Facts
- SNOMED CT
- 1296480005
- UMLS CUI
- C5848294
- Fully Specified Name
- Familial hyperinsulinemic hypoglycemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.