Persistent hyperinsulinemic hypoglycemia of infancy

disorder

SNOMED 360339005CUI C3888018

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Hyperinsulinemia hypoglycemia

Always present (100%)HP:0000825

Nesidioblastosis

Always present (100%)HP:0034346

Fetal macrosomia

HP:0001520

Hypoglycemic coma

HP:0001325

Hypoglycemic seizures

HP:0002173

Islet of Langerhans hyperplasia

HP:0004510

Low blood sugar

HP:0001943

Poor school performance

HP:0001249

Related Conditions

Diazoxide-resistant hyperinsulinemic hypoglycemia(child)

Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form(child)

FHH - familial hyperinsulinemic hypoglycemia(parent)

Quick Facts

SNOMED CT: 360339005
UMLS CUI: C3888018
Fully Specified Name: Persistent hyperinsulinemic hypoglycemia of infancy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.