ICD-10 Diagnosis Code E74.8

Other specified disorders of carbohydrate metabolism

Diagnosis Code E74.8

ICD-10: E74.8
Short Description: Other specified disorders of carbohydrate metabolism
Long Description: Other specified disorders of carbohydrate metabolism
This is the 2018 version of the ICD-10-CM diagnosis code E74.8

Valid for Submission
The code E74.8 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Endocrine, nutritional and metabolic diseases (E00–E90)
    • Metabolic disorders (E70-E88)
      • Other disorders of carbohydrate metabolism (E74)

Information for Medical Professionals

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • Abnormal glucose tolerance test
  • ALG12-congenital disorder of glycosylation
  • alpha, alpha-Trehalase deficiency
  • Carbohydrate-deficient glycoprotein syndrome
  • Carbohydrate-deficient glycoprotein syndrome
  • Carbohydrate-deficient glycoprotein syndrome type I
  • Carbohydrate-deficient glycoprotein syndrome type I
  • Congenital disorder of glycosylation type 1c
  • 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
  • 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
  • Familial renal glucosuria
  • Glucose tolerance test = renal glycosuria
  • Glycerol intolerance
  • Glycerol kinase deficiency - contiguous gene syndrome
  • Glycerol kinase deficiency - isolated
  • Glycosuria during pregnancy - delivered
  • Glycosuria during pregnancy - delivered with postnatal complication
  • Glycosuria during pregnancy - not delivered
  • Glycosuria during pregnancy with postnatal complication
  • Low renal threshold for glucose
  • Muscle phosphoglycerate mutase deficiency
  • Nonglucosuric melituria
  • Pentose disorder
  • Pregnancy-related glycosuria
  • Renal diabetes
  • Renal glucosuria, type A
  • Renal glucosuria, type B
  • Renal glucosuria, type O
  • Renal glycosuria
  • Renal glycosuria
  • Syndrome of carbohydrate intolerance
  • Xylosuria

Index of Diseases and Injuries
References found for the code E74.8 in the Index of Diseases and Injuries:

Information for Patients

Carbohydrate Metabolism Disorders

Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system (enzymes) break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues. If you have a metabolic disorder, something goes wrong with this process.

Carbohydrate metabolism disorders are a group of metabolic disorders. Normally your enzymes break carbohydrates down into glucose (a type of sugar). If you have one of these disorders, you may not have enough enzymes to break down the carbohydrates. Or the enzymes may not work properly. This causes a harmful amount of sugar to build up in your body. That can lead to health problems, some of which can be serious. Some of the disorders are fatal.

These disorders are inherited. Newborn babies get screened for many of them, using blood tests. If there is a family history of one of these disorders, parents can get genetic testing to see whether they carry the gene. Other genetic tests can tell whether the fetus has the disorder or carries the gene for the disorder.

Treatments may include special diets, supplements, and medicines. Some babies may also need additional treatments, if there are complications. For some disorders, there is no cure, but treatments may help with symptoms.

[Read More]
Previous Code
Previous Code E74.4
Next Code
E74.9 Next Code