1. Certain infectious and parasitic diseases (A00-B99)
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2. Neoplasms (C00-D48)
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3. Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
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4. Endocrine, nutritional and metabolic diseases (E00-E90)
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E00-E07 Disorders of thyroid gland
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E10-E14 Diabetes mellitus
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E15-E16 Other disorders of glucose regulation and pancreatic internal secretion
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E20-E35 Disorders of other endocrine glands
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E40-E46 Malnutrition
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E50-E64 Other nutritional deficiencies
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E65-E68 Obesity and other hyperalimentation
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E70-E90 Metabolic disorders
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E70 Disorders of aromatic amino-acid metabolism
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E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
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E72 Other disorders of amino-acid metabolism
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E73 Lactose intolerance
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E74 Other disorders of carbohydrate metabolism
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H00069 Glycogen storage diseases
H01760 Hepatic glycogen storage disease
H01762 Muscle glycogen storage disease
H01939 Glycogen storage disease type I
H01940 Glycogen storage disease type II
H01941 Glycogen storage disease type III
H01942 Glycogen storage disease type IV
H01943 Glycogen storage disease type V
H01944 Glycogen storage disease type VI
H01945 Glycogen storage disease type VII
H01948 Glycogen storage disease type IX
H01951 Glycogen storage disease type X
H01946 Glycogen storage disease type XI
H01952 Glycogen storage disease type XII
H01953 Glycogen storage disease type XIII
H01954 Glycogen storage disease type XIV
H01955 Glycogen storage disease type XV
H01950 Glycogen storage disease type 0a
H01949 Glycogen storage disease type 0b
H01956 Glycogen storage disease of heart
H01947 Fanconi-Bickel syndrome
H00150 Danon disease
H00071 Hereditary fructose intolerance
H00114 Fructose-1,6-bisphosphatase deficiency
H00070 Galactosemia
H02008 Galactose-1P uridylyltransferase deficiency
H02009 Galactokinase deficiency
H02010 Galactose epimerase deficiency
H00115 Congenital sucrase-isomaltase deficiency
H00072 Pyruvate dehydrogenase complex deficiency
H01997 Pyruvate dehydrogenase E1-alpha deficiency
H01998 Pyruvate dehydrogenase E1-beta deficiency
H01999 Pyruvate dehydrogenase E2 deficiency
H02003 Pyruvate dehydrogenase E3-binding protein deficiency
H01996 Pyruvate dehydrogenase phosphatase deficiency
H00073 Pyruvate carboxylase deficiency
H00117 Primary hyperoxaluria (HP)
H00552 Chromosome Xp21 deletion syndrome
H02013 Glycerol kinase deficiency
H01065 Pentosuria
H01126 Familial renal glucosuria (FRG)
H01189 Transaldolase (TALDO) deficiency
H01261 Congenital glucose-galactose malabsorption (GGM)
H02090 Trehalase deficiency
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E75 Disorders of sphingolipid metabolism and other lipid storage disorders
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E76 Disorders of glycosaminoglycan metabolism
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E77 Disorders of glycoprotein metabolism
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E78 Disorders of lipoprotein metabolism and other lipidaemias
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E79 Disorders of purine and pyrimidine metabolism
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E80 Disorders of porphyrin and bilirubin metabolism
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E83 Disorders of mineral metabolism
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E84 Cystic fibrosis
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E85 Amyloidosis
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E88 Other metabolic disorders
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5. Mental and behavioural disorders (F00-F99)
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6. Diseases of the nervous system (G00-G99)
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7. Diseases of the eye and adnexa (H00-H59)
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8. Diseases of the ear and mastoid process (H60-H95)
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9. Diseases of the circulatory system (I00-I99)
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10. Diseases of the respiratory system (J00-J99)
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11. Diseases of the digestive system (K00-K93)
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12. Diseases of the skin and subcutaneous tissue (L00-L99)
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13. Diseases of the musculoskeletal system and connective tissue (M00-M99)
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14. Diseases of the genitourinary system (N00-N99)
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15. Pregnancy, childbirth and the puerperium (O00-O99)
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16. Certain conditions originating in the perinatal period (P00-P96)
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17. Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
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18. Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R99)
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19. Injury, poisoning and certain other consequences of external causes (S00-T98)
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20. External causes of morbidity and mortality (V01-Y98)
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21. Factors influencing health status and contact with health services (Z00-Z99)
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22. Codes for special purposes (U00-U85)
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