Pancreatic endocrine cell hyperplasia
Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency
Ectopic IGF-1 hypoglycemia
Hyperinsulinaemia due to malignant insulinoma
Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency
Hyperinsulinism due to uncoupling protein 2 deficiency
Diazoxide-sensitive diffuse hyperinsulinism
Hypoglycemia
Tumor-induced hypoglycemia
Hyperinsulinism NOS
Post hypoglycaemic hyperglycaemia due to diabetes mellitus
Postprandial hypoglycaemia
Tumour-induced hypoglycaemia
Ketotic hypoglycemia
Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonaemia syndrome
Increased insulin
Hyperinsulinemic hypoglycaemia, diazoxide-resistant focal form
Pancreatic beta cell hyperplasia
Ketotic hypoglycaemia
Hyperinsulinemia
Fasting hypoglycaemia
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Hyperplasia of pancreatic islet beta cell (disorder)
Hyperammonaemia
Hyperinsulinaemia due to ectopic tumour source
Tumour-induced hyperinsulinaemia
Diazoxide-resistant hyperinsulinism
Non-diabetic hypoglycemia
insulin high
Pancreatic islet beta cell hyperplasia
Exercise-induced hyperinsulinemic hypoglycemia
Recurrent severe hypoglycemia
Ectopic insulin-like growth factor-1 hypoglycemia
Ectopic IGF hypoglycaemia
Post hypoglycemic hyperglycemia due to diabetes mellitus
Somogyi phenomenon
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency
Hyperinsulinism due to UCP2 deficiency
Hyperinsulinism
increasing insulin
Idiopathic postprandial hypoglycemia
Fasting hypoglycemia
Diazoxide-resistant diffuse hyperinsulinism
Ectopic IGF hypoglycemia
Autosomal recessive hyperinsulinemic hypoglycaemia due to SUR1 deficiency
Non-diabetic hypoglycaemia
Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency
Ectopic IGF-1 hypoglycaemia
Hypoglycaemia of childhood
Alimentary hyperinsulinemia
Hyperammonemia
Iatrogenic hyperinsulinism
Hyperplasia of pancreatic islet beta cell
Hyperinsulinism due to glucokinase deficiency
Functional nonhyperinsulinemic hypoglycemia
FHH - familial hyperinsulinemic hypoglycemia
Mixed hypoglycaemia
high insulin
GLUD1 related hyperinsulinism and hyperammonaemia syndrome
Post-prandial hypoglycemia
Post-prandial hypoglycaemia
Exercise-induced hyperinsulinism
Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonemia syndrome
Hyperinsulinism due to INSR (insulin receptor) deficiency
Hyperinsulinemia due to malignant insulinoma
Hypoglycemia due to neoplasm
Hyperinsulinism (disorder)
FHH - familial hyperinsulinemic hypoglycaemia
Hypoglycemia of childhood
Ectopic hyperinsulinemia
Post gastrointestinal tract surgery hypoglycaemia
Ectopic insulin-like growth factor-2 hypoglycemia
Hyperinsulinaemia
Hyperinsulinism and hyperammonaemia syndrome
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Hyperinsulinemic hypoglycaemia, diazoxide-resistant diffuse form
Diazoxide-resistant focal hyperinsulinism
GLUD1 related hyperinsulinism and hyperammonemia syndrome
Alimentary hyperinsulinaemia
Autosomal recessive hyperinsulinemic hypoglycaemia due to Kir6.2 deficiency
Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form
Hypoglycemia of infancy
Elevated insulin levels
Hyperinsulinism and hyperammonemia syndrome
Insulin increased
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
Idiopathic postprandial hypoglycaemia
Hyperinsulinism syndrome
Diazoxide-resistant hyperinsulinemic hypoglycaemia
Hypoglycaemia of infancy
Hyperinsulinemic hypoglycaemia due to Kir6.2 deficiency, diazoxide-resistant focal form
Tumor-induced hyperinsulinemia
Hypoglycaemia due to neoplasm
Neuroglycopenia
Hyperinsulinemic hypoglycemia due to SUR1 deficiency, diazoxide-resistant focal form
Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency
Recurrent severe hypoglycaemia
Hypoglycemic reaction
Ectopic insulin-like growth factor hypoglycemia
Hyperinsulinism due to insulin receptor deficiency
Autosomal recessive hyperinsulinism due to SUR1 deficiency
Exercise-induced hyperinsulinaemic hypoglycaemia
Elevated insulin level
hyperinsulism
Ectopic hyperinsulinism
Hyperinsulinemic hypoglycaemia, diazoxide-sensitive diffuse form
Hyperglycemia due to diabetes mellitus
Hyperinsulinism due to HNF1A deficiency
Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency
Metabolic complication of procedures
Autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency
Hyperinsulinism due to HNF4A deficiency
Postprandial hypoglycemia
Mixed hypoglycemia
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
Diazoxide-resistant hyperinsulinemic hypoglycemia
Ectopic insulin-like growth factor-1 hypoglycaemia
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
Hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form
Hyperinsulinemia due to ectopic tumor source
Impaired glucose tolerance with hyperinsulism
Hyperinsulinemic hypoglycemia, diazoxide-resistant diffuse form
Autoimmune hypoglycemia
Ectopic IGF-2 hypoglycaemia
Hyperinsulinemic hypoglycemia, diazoxide-resistant focal form
Functional hyperinsulinemia
Hyperinsulinemic hypoglycaemia due to SUR1 deficiency, diazoxide-resistant focal form
Hypoglycaemia
Ectopic insulin-like growth factor hypoglycaemia
Autoimmune hypoglycaemia
Ectopic insulin-like growth factor-2 hypoglycaemia
Functional hyperinsulinaemia
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Ectopic IGF-2 hypoglycemia
Functional hyperinsulinism
Hypoglycaemic reaction
Familial hyperinsulinemic hypoglycemia
Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
Nesidioblastosis
Islet cell hyperplasia
Alimentary hypoglycemia
Post gastrointestinal tract surgery hypoglycemia
Reactive hypoglycemia
Iatrogenic hyperinsulinaemia
Non-diabetic disorder of endocrine pancreas
Hyperinsulinism due to focal adenomatous hyperplasia
Familial hyperinsulinemic hypoglycaemia
Iatrogenic hyperinsulinemia
Hyperinsulinism due to deficiency of glucokinase
Functional hyperinsulinism (disorder)
Reactive hypoglycaemia
Hyperplasia of pancreatic islet beta cells NOS
Hyperglycaemia due to diabetes mellitus
Ectopic hyperinsulinaemia
Alimentary hypoglycaemia

Frequently Asked Questions

What is the ICD-10 code for other hypoglycemia?

The ICD-10-CM code for other hypoglycemia is E16.1. The full clinical description is "Other hypoglycemia". E16.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E16.1 mean?

ICD-10-CM code E16.1 represents “Other hypoglycemia”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E16.1 a billable code?

Yes, E16.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E16.1 in?

E16.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E16.1?

E16.1 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); diabetes with hypoglycemia (E08.649, E10.649, E11.649, E13.649); hypoglycemia in infant of diabetic mother (P70.1); and 1 more.

Are additional codes required with E16.1?

Yes, when using E16.1, also report: hypoglycemia level, if applicable (E16.A-).

What SNOMED CT codes does E16.1 map to?

E16.1 maps to 52 SNOMED CT concepts: 237647008, 237639008, 71858003, 717045004, 717046003, and 47 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E16.1?

E16.1 is linked to 5 UMLS Concept Unique Identifiers: C0020459, C0271705, C2874178, C0271706, C0348452. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E16.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other hypoglycemia affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E16.1?

E16.1 maps to the ICD-11 code: 5A4Z (Disorders of glucose regulation or pancreatic internal secretion, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.