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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
- E80.20 Unspecified porphyria
- 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' (
