E79 – Disorders of purine and pyrimidine metabolism
Coding Notes
Active
Non-billable / Non-specific, not valid for HIPAA-covered transactions
Type 1 Excludes
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)
Child Codes
Sibling Codes
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
Type 1 Excludes
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)
|
| 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 |
| E79.9 | Disorder of purine and pyrimidine metabolism, unspecified |