P70.4
BillableOther neonatal hypoglycemia
Other neonatal hypoglycemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Transitory neonatal hypoglycemia
Includes
Conditions included under this code
- conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth) even if morbidity occurs later
- transitory endocrine and metabolic disturbances caused by the infant's response to maternal endocrine and metabolic factors, or its adjustment to extrauterine environment
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(6)
P70.0Syndrome of infant of mother with gestational diabetes
P70.1Syndrome of infant of a diabetic mother
P70.2Neonatal diabetes mellitus
P70.3Iatrogenic neonatal hypoglycemia
P70.8Oth transitory disorders of carbohydrate metab of newborn
P70.9Transitory disorder of carbohydrate metab of newborn, unsp
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(89)
SNOMED CT
- Ketotic hypoglycaemia20825002
- Ketotic hypoglycemia20825002
- Fanconi syndrome40488004
- Neonatal hypoglycaemia52767006
- Neonatal hypoglycemia52767006
- Hypoglycaemic encephalopathy64624009
- Hypoglycemic encephalopathy64624009
- Spontaneous hypoglycaemia111559003
- Spontaneous hypoglycemia111559003
- Hypoinsulinism123762005
- Non-diabetic hypoglycaemia237637005
- Non-diabetic hypoglycemia237637005
- Transitory neonatal hypoglycaemia276561008
- Transitory neonatal hypoglycemia276561008
- Congenital hyperinsulinism360339005
- Congenital isolated hyperinsulinism360339005
- Persistent hyperinsulinaemic hypoglycaemia of infancy360339005
- Persistent hyperinsulinemic hypoglycemia of infancy360339005
- Hypoglycaemic shock360546002
- Hypoglycemic shock360546002
- Insulin shock360546002
- Neonatal renal disorder363224005
- Sequelae of endocrine disorders363297005
- Autosomal dominant hyperinsulinism due to SUR1 deficiency717046003
- Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency717046003
- Hyperinsulinism due to HNF4A deficiency717048002
- Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency717048002
- Hyperinsulinism due to deficiency of glucokinase717182006
- Hyperinsulinism due to glucokinase deficiency717182006
- Transient hyperinsulinaemic neonatal hypoglycaemia735496003
- Transient hyperinsulinemic neonatal hypoglycemia735496003
- Transient neonatal hypoglycaemia due to hyperinsulinaemia735496003
- Transient neonatal hypoglycemia due to hyperinsulinemia735496003
- Hypoinsulinemic hypoglycaemia and body hemihypertrophy773666007
- Hypoinsulinemic hypoglycemia and body hemihypertrophy773666007
- Glycopenia1217061002
- Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome1269271003
- Diazoxide-sensitive diffuse hyperinsulinism1363361006
- Hyperinsulinemic hypoglycaemia, diazoxide-sensitive diffuse form1363361006
- Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form1363361006
- Transient neonatal disorder of endocrine system16863181000119109
- Transient neonatal endocrine disorder16863181000119109
UMLS
Clinical Terms
- Hypoglycemic shock
- Autosomal dominant hyperinsulinism due to SUR1 deficiency
- Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency
- Diazoxide-sensitive diffuse hyperinsulinism
- Non-diabetic hypoglycaemia
- Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency
- Fanconi syndrome
- Ketotic hypoglycemia
- Transitory neonatal hypoglycemia
- Transient hyperinsulinaemic neonatal hypoglycaemia
- Hyperinsulinism due to glucokinase deficiency
- Transient neonatal hypoglycaemia due to hyperinsulinaemia
- Persistent hyperinsulinemic hypoglycemia of infancy
- Neonatal hypoglycemia
- Transient neonatal disorder of endocrine system
- Neonatal renal disorder
- Ketotic hypoglycaemia
- Transient neonatal endocrine disorder
- Persistent hyperinsulinaemic hypoglycaemia of infancy
- Congenital hyperinsulinism
- Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome
- Hypoglycaemic shock
- Transient neonatal hypoglycemia due to hyperinsulinemia
- Transitory neonatal hypoglycemia (disorder)
- Hypoinsulinemic hypoglycaemia and body hemihypertrophy
- Hypoglycaemic encephalopathy
- Non-diabetic hypoglycemia
- Congenital isolated hyperinsulinism
- Glycopenia
- Hyperinsulinemic hypoglycaemia, diazoxide-sensitive diffuse form
- Hyperinsulinism due to HNF4A deficiency
- Hypoinsulinemic hypoglycemia and body hemihypertrophy
- Spontaneous hypoglycaemia
- Sequelae of endocrine disorders
- Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form
- Transient hyperinsulinemic neonatal hypoglycemia
- Transitory neonatal hypoglycaemia
- Hyperinsulinism due to deficiency of glucokinase
- Hypoglycemic encephalopathy
- Neonatal hypoglycaemia
- Spontaneous hypoglycemia
- Hypoinsulinism
- Insulin shock
Frequently Asked Questions
What is the ICD-10 code for other neonatal hypoglycemia?
The ICD-10-CM code for other neonatal hypoglycemia is P70.4. The full clinical description is "Other neonatal hypoglycemia". P70.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P70.4 mean?
ICD-10-CM code P70.4 represents “Other neonatal hypoglycemia”. It is classified under Chapter 16: Certain Conditions Originating in the Perinatal Period and is a billable/specific code that can be used on a claim.
Is P70.4 a billable code?
Yes, P70.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P70.4 in?
P70.4 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What SNOMED CT codes does P70.4 map to?
P70.4 maps to 21 SNOMED CT concepts: 1269271003, 717046003, 360339005, 1363361006, 40488004, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P70.4?
P70.4 is linked to 2 UMLS Concept Unique Identifiers: C0477943, C0475721. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does P70.4 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other neonatal 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 P70.4?
P70.4 maps to the ICD-11 code: KB60.4Z (Neonatal hypoglycaemia, 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.