`E79.8` Other disorders of purine and pyrimidine metabolism

Non-billable header with 3 child codes.

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)

Codes under E79.8

Type 1 Excludes: E72 Other disorders of amino-acid metabolism ("purine and pyrimidine metabolism (E79.-)")
Type 2 Excludes: G11 Hereditary ataxia ("metabolic disorders (E70-E88)")
Type 2 Excludes: G11.3 Cerebellar ataxia with defective DNA repair ("other disorders of purine and pyrimidine metabolism (E79.-)")
Code First: G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")
Type 2 Excludes: G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")
Code First: H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")
Type 2 Excludes: N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")
Type 2 Excludes: N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")
Type 1 Excludes: P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")

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 (this code)
E79.81 Aicardi-Goutieres syndrome
E79.82 Hereditary xanthinuria
E79.89 Other specified disorders of purine and pyrimidine metabolism
E79.9 Disorder of purine and pyrimidine metabolism, unspecified