ICD-10 Code | E79 |
Description | Disorders of purine and pyrimidine metabolism |
Hierarchy | |
Billable status | Non billable code |
Type 1transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Type 1androgen insensitivity syndrome (E34.5-)
Type 1congenital adrenal hyperplasia (E25.0)
Type 1hemolytic anemias attributable to enzyme disorders (D55.-)
Type 1Marfan syndrome (Q87.4-)
Type 15-alpha-reductase deficiency (E29.1)
Type 2Ehlers-Danlos syndromes (Q79.6-)
Type 1Ataxia-telangiectasia (Q87.19)
Type 1Bloom's syndrome (Q82.8)
Type 1Cockayne's syndrome (Q87.19)
Type 1calculus of kidney (N20.0)
Type 1combined immunodeficiency disorders (D81.-)
Type 1Fanconi's anemia (D61.09)
Type 1gout (M1A.-, M10.-)
Type 1orotaciduric anemia (D53.0)
Type 1progeria (E34.8)
Type 1Werner's syndrome (E34.8)
Type 1xeroderma pigmentosum (Q82.1)