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E79 Disorders of purine and pyrimidine metabolism
BackE79.0Hyperuricemia without signs of inflammatory arthritis and tophaceous diseaseCategoryE79.1Lesch-Nyhan syndromeCategoryE79.2Myoadenylate deaminase deficiencyCategoryE79.8Other disorders of purine and pyrimidine metabolismCategory3 →E79.81Aicardi-Goutières syndromeCategoryE79.82Hereditary xanthinuriaCategoryE79.89Other specified disorders of purine and pyrimidine metabolismCategoryE79.9Disorder of purine and pyrimidine metabolism, unspecifiedCategory
Category
E79
Disorders of purine and pyrimidine metabolism
EXCLUDES
Excludes1: Ataxia-telangiectasia (Q87.19)
Bloom's syndrome (Q82.8)
Cockayne's syndrome (Q87.19)
calculus of kidney (N20.0)
combined immunodeficiency disorders (D81.-)
Fanconi's anemia (D61.09)
gout (M1A.-, M10.-)
orotaciduric anemia (D53.0)
progeria (E34.8)
Werner's syndrome (E34.8)
xeroderma pigmentosum (Q82.1)
Bloom's syndrome (Q82.8)
Cockayne's syndrome (Q87.19)
calculus of kidney (N20.0)
combined immunodeficiency disorders (D81.-)
Fanconi's anemia (D61.09)
gout (M1A.-, M10.-)
orotaciduric anemia (D53.0)
progeria (E34.8)
Werner's syndrome (E34.8)
xeroderma pigmentosum (Q82.1)
- Chapter
- IV · Endocrine, nutritional and metabolic diseases
- Section
- E70-E88
- Valid from
Source
CMS ICD-10-CM Tabular List, edition FY2026.