E74.4

Billable

Disorders of pyruvate metabolism and gluconeogenesis

Disorders of pyruvate metabolism and gluconeogenesis

Status

Billable / Specific

Block

E70-E88

Parent Code

E74

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Deficiency of phosphoenolpyruvate carboxykinase
  • Deficiency of pyruvate carboxylase
  • Deficiency of pyruvate dehydrogenase

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(6)
E74.0

Glycogen storage disease

E74.1

Disorders of fructose metabolism

E74.2

Disorders of galactose metabolism

E74.3

Other disorders of intestinal carbohydrate absorption

E74.8

Other specified disorders of carbohydrate metabolism

E74.9

Disorder of carbohydrate metabolism, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

5C53.0ZDisorders of pyruvate metabolism, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(203)

SNOMED CT

UMLS

Clinical Terms

  • PDHC deficiency
  • Pyruvate carboxylase deficiency disease
  • Deficiency of pyruvic carboxylase
  • Deficiency Disease, Pyruvate Carboxylase
  • PDH Deficiency
  • Intermittent ataxia with pyruvate dehydrogenase deficiency
  • PYRUVATE CARBOXYLASE DEFICIENCY
  • PDHC DEFIC DIS
  • PYRUVATE CARBOXYLASE DEFIC DIS
  • Phosphoenolpyruvate carboxykinase deficiency (disorder)
  • Type II Ataxia with Lactic Acidosis
  • PC - Pyruvate carboxylase deficiency
  • Deficiency, PDH
  • Ataxia with Lactic Acidosis 2
  • Deficiency of L-lactate dehydrogenase (cytochrome)
  • Deficiency, Pyruvate Dehydrogenase
  • PYRUVATE DECARBOXYLASE DEFICIENCY
  • Deficiency of pyruvate decarboxylase
  • Pyruvate dehydrogenase complex E1-alpha subunit deficiency
  • Deficiency of D-lactate dehydrogenase
  • Ataxia, Intermittent, with Pyruvate Dehydrogenase, or Decarboxylase, Deficiency
  • Deficiency of pyruvic decarboxylase
  • Deficiency of lactate racemase
  • PEPCK - Phosphoenolpyruvate carboxykinase deficiency
  • Deficiency of lacticoracemase
  • Deficiency of D-lactic acid dehydrogenase
  • Pyruvate dehydrogenase phosphatase deficiency
  • Mitochondrial pyruvate carrier deficiency
  • Pyruvate dehydrogenase complex deficiency (disorder)
  • Ataxia with lactic acidosis
  • Deficiency of pyruvate decarboxylase (disorder)
  • Pyruvate Dehydrogenase Deficiency
  • Deficiency of thioltransacetylase A
  • ATAXIA, INTERMITTENT, WITH PYRUVATE DEHYDROGENASE DEFICIENCY
  • PC deficiency
  • Phosphoenolpyruvate carboxykinase-1 (PCK1) deficiency
  • Pyruvate dehydrogenase complex deficiency
  • Pyruvate carboxylase deficiency (disorder)
  • Phosphoenolpyruvate carboxykinase deficiency
  • Muscle L-lactate dehydrogenase deficiency
  • Deficiency of phosphoenolpyruvate carboxykinase
  • Deficiency of lipoate acetyltransferase
  • Deficiency of lactic acid dehydrogenase
  • Deficiency of pyruvate dehydrogenase (cytochrome)
  • Deficiency of lactic acid dehydrogenase (cytochrome)
  • Lactic acid dehydrogenase deficiency
  • Pyruvate dehydrogenase complex E2 subunit deficiency
  • Phosphoenolpyruvate carboxylase deficiency
  • Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic
  • Phosphopyruvate carboxylase deficiency
  • Phosphoenolpyruvate carboxykinase (GTP) deficiency
  • ATAXIA WITH LACTIC ACIDOSIS II
  • PDH
  • LDH - Lactate dehydrogenase deficiency
  • Deficiency of pyruvate dehydrogenase
  • Deficiency, PDHC
  • Pyruvate dehydrogenase complex E1 beta subunit deficiency
  • Deficiency, Pyruvate Decarboxylase
  • PYRUVATE DEHYDROGENASE COMPLEX DEFIC DIS
  • Deficiency of alpha-ketoacid carboxylase
  • Deficiency of hydroxyacid racemase
  • Ataxia, Intermittent, with Abnormal Pyruvate Metabolism
  • Ataxia with lactic acidosis I
  • Ataxia with Lactic Acidosis, Type II
  • Disorder of pyruvate metabolism and mitochondrial respiratory chain
  • DEFIC DIS PYRUVATE CARBOXYLASE
  • Deficiency of pyruvate carboxylase
  • Deficiency of dihydrolipoamide acetyltransferase
  • Inborn error of pyruvate metabolism
  • Deficiency of pyruvic dehydrogenase
  • Deficiency of L-lactate dehydrogenase
  • Deficiency of acylphosphatase
  • PDH - Pyruvate dehydrogenase deficiency
  • Lactate dehydrogenase deficiency
  • Deficiency of glucose-1-phosphate phosphodismutase
  • Pyruvate Dehydrogenase Complex Deficiency Disease
  • Deficiency, Pyruvate Carboxylase
  • Deficiency of alpha-carboxylase
  • PDHC Deficiency Disease
  • Lactic Acidosis with Ataxia, Type II
  • Disorders of pyruvate metabolism and gluconeogenesis (disorder)
Frequently Asked Questions
What is the ICD-10 code for disorders of pyruvate metabolism and gluconeogenesis?

The ICD-10-CM code for disorders of pyruvate metabolism and gluconeogenesis is E74.4. The full clinical description is "Disorders of pyruvate metabolism and gluconeogenesis". E74.4 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E74.4 mean?

ICD-10-CM code E74.4 represents “Disorders of pyruvate metabolism and gluconeogenesis”. 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 E74.4 a billable code?

Yes, E74.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E74.4 in?

E74.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E74.4?

E74.4 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 9 more.

What SNOMED CT codes does E74.4 map to?

E74.4 maps to 21 SNOMED CT concepts: 46683007, 87694001, 124116001, 124115002, 124141008, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E74.4?

E74.4 is linked to 4 UMLS Concept Unique Identifiers: C0034341, C0034345, C0268194, C0348946. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E74.4 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorders of pyruvate metabolism and gluconeogenesis 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 E74.4?

E74.4 maps to the ICD-11 code: 5C53.0Z (Disorders of pyruvate metabolism, unspecified).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try FreeView API Docs

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.