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ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

E79.8 – Other disorders of purine and pyrimidine metabolism

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Applicable To

Hereditary xanthinuria

GEM Conversion to ICD-9 CM

Fs: 10000 – Other disorders of purine and pyrimidine metabolism

MDC / MS-DRG Reference

INBORN AND OTHER DISORDERS OF METABOLISM

Back Reference of Diagnostic Codes

Aciduria
orotic (congenital) (hereditary) (pyrimidine deficiency) E79.8
Calculus, calculi, calculous
xanthine E79.8
Disorder (of) See also Disease
metabolism NOS E88.9
purine E79.9
specified NEC E79.8
pyrimidine E79.9
specified NEC E79.8
Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) E79.8
Stone (s) See also Calculus
xanthine E79.8
Xanthinuria, hereditary E79.8

Sibling Codes

Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
Lesch-Nyhan syndrome
Myoadenylate deaminase deficiency
Disorder of purine and pyrimidine metabolism, unspecified

Parent Sibling Codes

Disorders of aromatic amino-acid metabolism
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Other disorders of amino-acid metabolism
Lactose intolerance
Other disorders of carbohydrate metabolism
Disorders of sphingolipid metabolism and other lipid storage disorders
Disorders of glycosaminoglycan metabolism
Disorders of glycoprotein metabolism
Disorders of lipoprotein metabolism and other lipidemias
Disorders of purine and pyrimidine metabolism

View in Tabular

Code Title
E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
E70-E88 Metabolic disorders (E70-E88)
E79 Disorders of purine and pyrimidine metabolism
E79.8 Other disorders of purine and pyrimidine metabolism
Applicable to
Hereditary xanthinuria