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  6. 2024 ICD-10-CM Code E74.89
Version 2024
Billable Code

2024 ICD-10-CM Diagnosis Code E74.89

Other specified disorders of carbohydrate metabolism

ICD-10-CM Code:
E74.89
ICD-10 Code for:
Other specified disorders of carbohydrate metabolism
Is Billable?
Yes - Valid for Submission
Chronic Condition Indicator: [1]
Chronic
Code Navigator:

Code Classification

  • Endocrine, nutritional and metabolic diseases
    (E00–E89)
    • Metabolic disorders
      (E70-E88)
      • Other disorders of carbohydrate metabolism
        (E74)

E74.89 is a billable diagnosis code used to specify a medical diagnosis of other specified disorders of carbohydrate metabolism. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024.

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • ALG1 congenital disorder of glycosylation
  • ALG12-congenital disorder of glycosylation
  • ALG3 congenital disorder of glycosylation
  • ALG8 congenital disorder of glycosylation
  • ALG9 congenital disorder of glycosylation
  • CCDC115 congenital disorder of glycosylation
  • COG1 congenital disorder of glycosylation
  • COG4 congenital disorder of glycosylation
  • COG5 congenital disorder of glycosylation
  • COG7 congenital disorder of glycosylation
  • COG8 congenital disorder of glycosylation
  • Congenital disorder of glycosylation type 1c
  • Congenital disorder of glycosylation type 1e
  • Congenital disorder of glycosylation type 1f
  • Congenital disorder of glycosylation type 1i
  • Congenital disorder of glycosylation type 1j
  • Congenital disorder of glycosylation type 1n
  • Congenital disorder of glycosylation type 1p
  • Congenital disorder of glycosylation type 1q
  • Congenital disorder of glycosylation type 1r
  • Congenital disorder of glycosylation type 1s
  • Congenital disorder of glycosylation type 1w
  • Congenital disorder of glycosylation type 1x
  • Congenital disorder of glycosylation type 1y
  • Deficiency of aldehyde reductase
  • Deficiency of aldonolactonase
  • Deficiency of aldose 1-epimerase
  • Deficiency of alpha-amylase
  • Deficiency of alpha-mannosidase
  • Deficiency of amylase
  • Deficiency of amylo-1,6-glucosidase
  • Deficiency of amylopectin 6-glucanohydrolase
  • Deficiency of benzaldehyde dehydrogenase
  • Deficiency of beta-amylase
  • Deficiency of beta-fructofuranosidase
  • Deficiency of beta-glucosidase
  • Deficiency of beta-glucuronidase
  • Deficiency of bisphosphoglycerate mutase
  • Deficiency of bisphosphoglycerate phosphatase
  • Deficiency of endo-1,3-beta-glucanase
  • Deficiency of glucan 1,3-alpha-glucosidase
  • Deficiency of glucokinase
  • Deficiency of gluconate 2-dehydrogenase
  • Deficiency of gluconokinase
  • Deficiency of gluconolactonase
  • Deficiency of glucosamine-6-phosphate isomerase
  • Deficiency of glucose dehydrogenase
  • Deficiency of glucose oxidase
  • Deficiency of glucose-1-phosphatase
  • Deficiency of glucose-6-phosphate isomerase
  • Deficiency of glucosyltransferase 1
  • Deficiency of glyceraldehyde-3-phosphate dehydrogenase
  • Deficiency of glycerol kinase
  • Deficiency of glycosidase
  • Deficiency of glycosulfatase
  • Deficiency of glycosyltransferase
  • Deficiency of maltose phosphorylase
  • Deficiency of mannokinase
  • Deficiency of phosphoglucokinase
  • Deficiency of phosphoglycerate kinase
  • Deficiency of phosphomannomutase 2
  • Deficiency of phosphorylase b kinase
  • Deficiency of protein kinase
  • Deficiency of rhamnulokinase
  • Deficiency of xylulokinase
  • D-Glyceric aciduria
  • Disacchariduria
  • Disorder of glucose metabolism
  • Disorder of glucose regulation
  • Disorder of glycerate metabolism
  • Disorder of glycerol metabolism
  • Essential pentosuria
  • Glycerol intolerance syndrome
  • Glycerol kinase deficiency - contiguous gene syndrome
  • Glycerol kinase deficiency - isolated
  • Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
  • Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
  • Muscle phosphoglycerate mutase deficiency
  • Nonglucosuric melituria
  • Pentose disorder
  • PGM1-related congenital disorder of glycosylation
  • Phosphoglucomutase 3-related congenital disorder of glycosylation
  • SLC35A1 congenital disorder of glycosylation
  • SLC39A8 congenital disorder of glycosylation
  • Solute carrier family 35 member A2 congenital disorder of glycosylation
  • Syndrome of carbohydrate intolerance
  • Trehalase deficiency
  • Xylosuria
  • XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation

Clinical Classification

Tabular List of Diseases and Injuries

The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.


Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • Essential pentosuria

Index to Diseases and Injuries References

The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).

Replacement Code

E7489 replaces the following previously assigned ICD-10-CM code(s):

  • E74.8 - Other specified disorders of carbohydrate metabolism

Code History

  • FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
  • FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
  • FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
  • FY 2021 - Code Added, effective from 10/1/2020 through 9/30/2021

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.