E74.4
BillableDisorders of pyruvate metabolism and gluconeogenesis
Disorders of pyruvate metabolism and gluconeogenesis
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)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- diabetes mellitus (E08-E13)
- hypoglycemia NOS (E16.2)
- increased secretion of glucagon (E16.3)
- mucopolysaccharidosis (E76.0-E76.3)
- disorders of pyruvate metabolism and gluconeogenesis with anemia (D55.-)
- Leigh's syndrome (G31.82)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- PEPCK - Phosphoenolpyruvate carboxykinase deficiency5335002
- Phosphoenolpyruvate carboxykinase (GTP) deficiency5335002
- Phosphoenolpyruvate carboxykinase deficiency5335002
- Ataxia with lactic acidosis46683007
- Ataxia with lactic acidosis I46683007
- Deficiency of pyruvate dehydrogenase (cytochrome)46683007
- Deficiency of pyruvic dehydrogenase46683007
- PDH - Pyruvate dehydrogenase deficiency46683007
- PDH deficiency46683007
- Pyruvate dehydrogenase complex deficiency46683007
- Pyruvate dehydrogenase deficiency46683007
- Inborn error of pyruvate metabolism53210006
- Muscle L-lactate dehydrogenase deficiency55783001
- Ataxia with lactic acidosis II87694001
- Deficiency of pyruvate carboxylase87694001
- Deficiency of pyruvic carboxylase87694001
- PC - Pyruvate carboxylase deficiency87694001
- PC deficiency87694001
- Pyruvate carboxylase deficiency87694001
- Deficiency of L-lactate dehydrogenase124115002
- Deficiency of lactic acid dehydrogenase124115002
- Deficiency of D-lactate dehydrogenase124116001
- Deficiency of D-lactic acid dehydrogenase124116001
- Deficiency of L-lactate dehydrogenase (cytochrome)124141008
- Deficiency of lactic acid dehydrogenase (cytochrome)124141008
- Deficiency of dihydrolipoamide acetyltransferase124261008
- Deficiency of lipoate acetyltransferase124261008
- Deficiency of thioltransacetylase A124261008
- Deficiency of glucose-1-phosphate phosphodismutase124332009
- Deficiency of acylphosphatase124533003
- Deficiency of alpha-carboxylase124593001
- Deficiency of alpha-ketoacid carboxylase124593001
- Deficiency of pyruvate decarboxylase124593001
- Deficiency of pyruvic decarboxylase124593001
- Deficiency of hydroxyacid racemase124659007
- Deficiency of lactate racemase124659007
- Deficiency of lacticoracemase124659007
- Disorders of pyruvate metabolism and gluconeogenesis190760009
- Disorder of pyruvate metabolism and mitochondrial respiratory chain237981000
- LDH - Lactate dehydrogenase deficiency237982007
- Lactate dehydrogenase deficiency237982007
- Lactic acid dehydrogenase deficiency237982007
- Pyruvate dehydrogenase phosphatase deficiency1003847003
- Pyruvate dehydrogenase complex E2 subunit deficiency1003849000
- Pyruvate dehydrogenase complex E1-alpha subunit deficiency1003850000
- Pyruvate dehydrogenase complex E1 beta subunit deficiency1003851001
- Mitochondrial pyruvate carrier deficiency1217212009
UMLS
- ATAXIA WITH LACTIC ACIDOSIS IIC0034341
- Ataxia with Lactic Acidosis 2C0034341
- Ataxia with Lactic Acidosis IIC0034341
- Ataxia with Lactic Acidosis, Type IIC0034341
- Ataxia with lactic acidosis IIC0034341
- Ataxia with lactic acidosis, type IIC0034341
- DEFIC DIS PYRUVATE CARBOXYLASEC0034341
- Deficiency Disease, Pyruvate CarboxylaseC0034341
- Deficiency of pyruvate carboxylaseC0034341
- Deficiency of pyruvic carboxylaseC0034341
- Deficiency, Pyruvate CarboxylaseC0034341
- Lactic Acidosis with Ataxia, Type IIC0034341
- PC - Pyruvate carboxylase deficiencyC0034341
- PC DEFICIENCYC0034341
- PC deficiencyC0034341
- PYRUVATE CARBOXYLASE DEFIC DISC0034341
- PYRUVATE CARBOXYLASE DEFICIENCYC0034341
- Pyruvate Carboxylase DeficiencyC0034341
- Pyruvate Carboxylase Deficiency DiseaseC0034341
- Pyruvate carboxylase deficiencyC0034341
- Pyruvate carboxylase deficiency (disorder)C0034341
- Pyruvate carboxylase deficiency diseaseC0034341
- Type II Ataxia with Lactic AcidosisC0034341
- Type II ataxia with lactic acidosisC0034341
- ATAXIA, INTERMITTENT, WITH ABNORMAL PYRUVATE METABOLISMC0034345
- ATAXIA, INTERMITTENT, WITH PYRUVATE DEHYDROGENASE DEFICIENCYC0034345
- Ataxia with lactic acidosisC0034345
- Ataxia with lactic acidosis IC0034345
- Ataxia, Intermittent, with Abnormal Pyruvate MetabolismC0034345
- Ataxia, Intermittent, with Pyruvate Dehydrogenase, or Decarboxylase, DeficiencyC0034345
- Deficiency of alpha-carboxylaseC0034345
- Deficiency of alpha-ketoacid carboxylaseC0034345
- Deficiency of pyruvate decarboxylaseC0034345
- Deficiency of pyruvate decarboxylase (disorder)C0034345
- Deficiency of pyruvate dehydrogenaseC0034345
- Deficiency of pyruvate dehydrogenase (cytochrome)C0034345
- Deficiency of pyruvic decarboxylaseC0034345
- Deficiency of pyruvic dehydrogenaseC0034345
- Deficiency, PDHC0034345
- Deficiency, PDHCC0034345
- Deficiency, Pyruvate DecarboxylaseC0034345
- Deficiency, Pyruvate DehydrogenaseC0034345
- Intermittent Ataxia with Pyruvate Dehydrogenase DeficiencyC0034345
- Intermittent ataxia with pyruvate dehydrogenase deficiencyC0034345
- PDHC0034345
- PDH - Pyruvate dehydrogenase deficiencyC0034345
- PDH DEFICIENCYC0034345
- PDH DeficiencyC0034345
- PDH deficiencyC0034345
- PDHC DEFIC DISC0034345
- PDHC DeficiencyC0034345
- PDHC Deficiency DiseaseC0034345
- PDHC deficiencyC0034345
- PYRUVATE DECARBOXYLASE DEFICIENCYC0034345
- PYRUVATE DEHYDROGENASE COMPLEX DEFIC DISC0034345
- PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCYC0034345
- Pyruvate Decarboxylase DeficiencyC0034345
- Pyruvate Dehydrogenase Complex DeficiencyC0034345
- Pyruvate Dehydrogenase Complex Deficiency DiseaseC0034345
- Pyruvate Dehydrogenase DeficiencyC0034345
- Pyruvate dehydrogenase complex deficiencyC0034345
- Pyruvate dehydrogenase complex deficiency (disorder)C0034345
- Pyruvate dehydrogenase deficiencyC0034345
- Deficiency of phosphoenolpyruvate carboxykinaseC0268194
- PEPCK - Phosphoenolpyruvate carboxykinase deficiencyC0268194
- Phosphoenolpyruvate Carboxykinase DeficiencyC0268194
- Phosphoenolpyruvate Carboxykinase Deficiency, CytosolicC0268194
- Phosphoenolpyruvate carboxykinase (GTP) deficiencyC0268194
- Phosphoenolpyruvate carboxykinase deficiencyC0268194
- Phosphoenolpyruvate carboxykinase deficiency (disorder)C0268194
- Phosphoenolpyruvate carboxykinase-1 (PCK1) deficiencyC0268194
- Phosphoenolpyruvate carboxylase deficiencyC0268194
- Phosphopyruvate carboxylase deficiencyC0268194
- Disorders of pyruvate metabolism and gluconeogenesisC0348946
- Disorders of pyruvate metabolism and gluconeogenesis (disorder)C0348946
Frequently Asked Questions
What is ICD-10 code E74.4?
ICD-10-CM code E74.4 represents "Disorders of pyruvate metabolism and gluconeogenesis". It 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.
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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.