Human Diseases in ICD-10 Classification

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 1. Certain infectious and parasitic diseases (A00-B99)
 2. Neoplasms (C00-D48)
 3. Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
 4. Endocrine, nutritional and metabolic diseases (E00-E90)
   E00-E07  Disorders of thyroid gland
   E10-E14  Diabetes mellitus
   E15-E16  Other disorders of glucose regulation and pancreatic internal secretion
   E20-E35  Disorders of other endocrine glands
   E40-E46  Malnutrition
   E50-E64  Other nutritional deficiencies
   E65-E68  Obesity and other hyperalimentation
   E70-E90  Metabolic disorders
     E70  Disorders of aromatic amino-acid metabolism
     E71  Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
     E72  Other disorders of amino-acid metabolism
     E73  Lactose intolerance
     E74  Other disorders of carbohydrate metabolism
       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
     E75  Disorders of sphingolipid metabolism and other lipid storage disorders
     E76  Disorders of glycosaminoglycan metabolism
     E77  Disorders of glycoprotein metabolism
     E78  Disorders of lipoprotein metabolism and other lipidaemias
     E79  Disorders of purine and pyrimidine metabolism
     E80  Disorders of porphyrin and bilirubin metabolism
     E83  Disorders of mineral metabolism
     E84  Cystic fibrosis
     E85  Amyloidosis
     E88  Other metabolic disorders
 5. Mental and behavioural disorders (F00-F99)
 6. Diseases of the nervous system (G00-G99)
 7. Diseases of the eye and adnexa (H00-H59)
 8. Diseases of the ear and mastoid process (H60-H95)
 9. Diseases of the circulatory system (I00-I99)
 10. Diseases of the respiratory system (J00-J99)
 11. Diseases of the digestive system (K00-K93)
 12. Diseases of the skin and subcutaneous tissue (L00-L99)
 13. Diseases of the musculoskeletal system and connective tissue (M00-M99)
 14. Diseases of the genitourinary system (N00-N99)
 15. Pregnancy, childbirth and the puerperium (O00-O99)
 16. Certain conditions originating in the perinatal period (P00-P96)
 17. Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
 18. Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R99)
 19. Injury, poisoning and certain other consequences of external causes (S00-T98)
 20. External causes of morbidity and mortality (V01-Y98)
 21. Factors influencing health status and contact with health services (Z00-Z99)
 22. Codes for special purposes (U00-U85)

Last updated: July 12, 2018
Classification taken from ICD-10 Version 2016

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