ICD-10 Diagnosis Code E79.8

Other disorders of purine and pyrimidine metabolism

Diagnosis Code E79.8

ICD-10: E79.8
Short Description: Other disorders of purine and pyrimidine metabolism
Long Description: Other disorders of purine and pyrimidine metabolism
This is the 2017 version of the ICD-10-CM diagnosis code E79.8

Code Classification
  • Endocrine, nutritional and metabolic diseases
    • Metabolic disorders (E70-E88)
      • Disorders of purine and pyrimidine metabolism (E79)

Information for Medical Professionals

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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.

  • Adenine phosphoribosyl transferase deficiency type I
  • Adenine phosphoribosyl transferase deficiency type II
  • Adenine phosphoribosyltransferase deficiency, Japanese type
  • Adenylosuccinate lyase deficiency
  • beta-Aminoisobutyricaciduria
  • Combined molybdoflavoprotein enzyme deficiency
  • Cytosine diphosphate choline phosphotransferase deficiency
  • Deficiency of 3'-nucleotidase
  • Deficiency of 5'-nucleotidase
  • Deficiency of adenine deaminase
  • Deficiency of adenine phosphoribosyltransferase
  • Deficiency of adenosine monophosphate deaminase
  • Deficiency of adenosine monophosphate nucleosidase
  • Deficiency of allantoicase
  • Deficiency of allantoinase
  • Deficiency of aspartate carbamoyltransferase
  • Deficiency of beta-ureidopropionase
  • Deficiency of cytidine deaminase
  • Deficiency of dihydrouracil dehydrogenase
  • Deficiency of glycine formiminotransferase
  • Deficiency of guanosine monophosphate synthase
  • Deficiency of phosphoribosylaminoimidazole carboxylase
  • Deficiency of phosphoribosylaminoimidazolecarboxamide formyltransferase
  • Deficiency of phosphoribosylaminoimidazole-succinocarboxamide synthase
  • Deficiency of phosphoribosylformylglycinamidine cyclo-ligase
  • Deficiency of phosphoribosylformylglycinamidine synthase
  • Deficiency of thymidine phosphorylase
  • Deficiency of trimetaphosphatase
  • Deficiency of uridine phosphorylase
  • Deficiency of xanthine oxidase
  • Dihydropyrimidinase deficiency
  • Dihydrouracil dehydrogenase
  • Disorder of pyrimidine metabolism
  • Disorder of pyrimidine metabolism
  • Disorder of pyrimidine metabolism
  • Disorder of pyrimidine metabolism
  • Disorder of pyrimidine metabolism
  • Hereditary orotic aciduria
  • Hereditary orotic aciduria, type 1
  • Hereditary orotic aciduria, type 2
  • Hereditary xanthinuria
  • Hyperuricuria
  • Hypouricemia
  • Inosine triphosphate pyrophosphohydrolase deficiency
  • Isolated xanthine oxidase deficiency
  • Orotic aciduria
  • Ribose-phosphate pyrophosphokinase overactivity
  • Secondary orotic aciduria
  • Thiopurine methyltransferase deficiency
  • Uridine monophosphate hydrolase deficiency
  • Xanthinuria

Index of Diseases and Injuries
References found for the code E79.8 in the Index of Diseases and Injuries:

Information for Patients

Metabolic Disorders

Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system 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, such as your liver, muscles, and body fat.

A metabolic disorder occurs when abnormal chemical reactions in your body disrupt this process. When this happens, you might have too much of some substances or too little of other ones that you need to stay healthy. There are different groups of disorders. Some affect the breakdown of amino acids, carbohydrates, or lipids. Another group, mitochondrial diseases, affects the parts of the cells that produce the energy.

You can develop a metabolic disorder when some organs, such as your liver or pancreas, become diseased or do not function normally. Diabetes is an example.

  • Acidosis
  • Alkalosis
  • Lactic acid test
  • Metabolic acidosis
  • Metabolic neuropathies
  • Pseudohypoparathyroidism

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