Diagnosis Code: E74.89

Short Description: Other specified disorders of carbohydrate metabolism

Long Description: Other specified disorders of carbohydrate metabolism

The code E74.89 is VALID for claim submission

Code Classification:

• Endocrine, nutritional and metabolic diseases (E00–E89)
  • Metabolic disorders (E70-E88)
    • Other disorders of carbohydrate metabolism (E74)
      • E74.89 Other specified disorders of carbohydrate metabolism

Code Version: 2022 ICD-10-CM

Synonyms

• 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

References to Index of Diseases and Injuries

The code E74.89 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Essential pentosuria

Similar Codes

This page was last updated on: 10/1/2023

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