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Diagnosis Code

E79.82 HEREDITARY XANTHINURIA


Code Information

Diagnosis Code: E79.82

Short Description: Hereditary xanthinuria

Long Description: Hereditary xanthinuria

The code E79.82 is VALID for claim submission

Code Classification:

  • Endocrine, nutritional and metabolic diseases (E00–E89)
    • Metabolic disorders (E70-E88)
      • Disorders of purine and pyrimidine metabolism (E79)
        • E79.82 Hereditary xanthinuria

Code Version: 2022 ICD-10-CM


Synonyms

  • Combined molybdoflavoprotein enzyme deficiency
  • Deficiency of xanthine oxidase
  • Deficiency of xanthine oxidase
  • Deficiency of xanthine oxidase
  • Deficiency of xanthine oxidase
  • Deficiency of xanthine oxidase
  • Deficiency of xanthine oxidase
  • Hereditary xanthinuria
  • Hereditary xanthinuria type 1
  • Molybdenum cofactor deficiency complementation group A
  • Molybdenum cofactor deficiency complementation group B
  • Molybdenum cofactor deficiency complementation group C
  • Xanthinuria

Similar Codes

ICD-10 Code ICD-10 Description
E79 Disorders of purine and pyrimidine metabolism
E79.0 Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
E79.1 Lesch-Nyhan syndrome
E79.2 Myoadenylate deaminase deficiency
E79.8 Other disorders of purine and pyrimidine metabolism
E79.81 Aicardi-Goutieres syndrome
E79.89 Other specified disorders of purine and pyrimidine metabolism
E79.9 Disorder of purine and pyrimidine metabolism, unspecified

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

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