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 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
 * Asymptomatic hyperuricemia
 * E79.1 Lesch-Nyhan syndrome
 * HGPRT deficiency
 * E79.2 Myoadenylate deaminase deficiency
 * E79.8 Other disorders of purine and pyrimidine metabolism
 * Hereditary xanthinuria
 * E79.9 Disorder of purine and pyrimidine metabolism, unspecified

E80 Disorders of porphyrin and bilirubin metabolism

 * Includes: defects of catalase and peroxidase
 * E80.0 Hereditary erythropoietic porphyria
 * Congenital erythropoietic porphyria
 * Erythropoietic protoporphyria
 * E80.1 Porphyria cutanea tarda
 * E80.2 Other and unspecified porphyria
 * E80.20 Unspecified porphyria
 * Porphyria NOS
 * E80.21 Acute intermittent (hepatic) porphyria
 * E80.29 Other porphyria
 * Hereditary coproporphyria
 * E80.3 Defects of catalase and peroxidase
 * Acatalasia [Takahara]
 * E80.4 Gilbert's syndrome
 * E80.5 Crigler-Najjar syndrome
 * E80.6 Other disorders of bilirubin metabolism
 * Dubin-Johnson syndrome
 * Rotor's syndrome
 * E80.7 Disorder of bilirubin metabolism, unspecified

E83 Disorders of mineral metabolism

 * Excludes1: dietary mineral deficiency (E58-E61)
 * parathyroid disorders (E20-E21)
 * vitamin D deficiency (E55.-)
 * E83.0 Disorders of copper metabolism
 * E83.00 Disorder of copper metabolism, unspecified
 * E83.01 Wilson's disease
 * Code also associated Kayser Fleischer ring (H18.04-)
 * E83.09 Other disorders of copper metabolism
 * Menkes' (