Human Diseases in ICD-11 Classification

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 01 Certain infectious or parasitic diseases
 
 02 Neoplasms
 
 03 Diseases of the blood or blood-forming organs
 
 04 Diseases of the immune system
 
 05 Endocrine, nutritional or metabolic diseases
   Endocrine diseases
   Nutritional disorders
   Metabolic disorders
     Inborn errors of metabolism
       5C50  Inborn errors of amino acid or other organic acid metabolism
       5C51  Inborn errors of carbohydrate metabolism
       5C52  Inborn errors of lipid metabolism
         H01589  Systemic primary carnitine deficiency
         H01981  Carnitine palmitoyltransferase I deficiency
         H01982  Carnitine palmitoyltransferase II deficiency
         H01983  Carnitine-acylcarnitine translocase deficiency
         H00392  VLCAD deficiency
         H00488  MCAD deficiency
         H00489  LCHAD deficiency
         H00525  Disorders of mitochondrial fatty-acid oxidation
         H00925  2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency
         H01352  Mitochondrial trifunctional protein deficiency
         H01364  3-Hydroxyacyl-CoA dehydrogenase deficiency
         H01929  2,4-Dienoyl-CoA reductase deficiency
         H01980  SCAD deficiency
         H02085  Acyl-CoA dehydrogenase 9 deficiency
         H00179  3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
         H01121  Succinyl CoA:3-oxoacid CoA transferase (SCOT) deficiency
         H01123  HMG-CoA synthase deficiency
         H00162  Sjogren-Larsson syndrome
         H02284  Leukotriene C4 synthase deficiency
         H00161  Smith-Lemli-Opitz syndrome
         H00206  Mevalonate kinase deficiency
         H00617  Desmosterolosis
         H01281  Lathosterolosis
         H00151  Cerebrotendinous xanthomatosis
         H00624  Progressive familial intrahepatic cholestasis
         H00628  Congenital bile acid synthesis defect
         H02099  Alpha-methylacyl-CoA racemase deficiency
         H00152  Sitosterolemia
         H00736  Dorfman-Chanarin syndrome
         H01297  Neutral lipid storage disease with myopathy
         H00654  Barth syndrome
       5C53  Inborn errors of energy metabolism
       5C54  Inborn errors of glycosylation or other specified protein modification
       5C55  Inborn errors of purine, pyrimidine or nucleotide metabolism
       5C56  Lysosomal diseases
       5C57  Peroxisomal diseases
       5C58  Inborn errors of porphyrin or heme metabolism
       5C59  Inborn errors of neurotransmitter metabolism
       5C5A  Alpha-1-antitrypsin deficiency
       5C5Y  Other specified inborn errors of metabolism
       5C5Z  Inborn errors of metabolism, unspecified
     Disorders of metabolite absorption or transport
     Disorders of fluid, electrolyte or acid-base balance
     Disorders of lipoprotein metabolism or certain specified lipidaemias
     5C90  Metabolic or transporter liver disease
     Other metabolic disorders
     5D2Z  Metabolic disorders, unspecified
   Postprocedural endocrine or metabolic disorders
 
 06 Mental, behavioural or neurodevelopmental disorders
 
 07 Sleep-wake disorders
 
 08 Diseases of the nervous system
 
 09 Diseases of the visual system
 
 10 Diseases of the ear or mastoid process
 
 11 Diseases of the circulatory system
 
 12 Diseases of the respiratory system
 
 13 Diseases of the digestive system
 
 14 Diseases of the skin
 
 15 Diseases of the musculoskeletal system or connective tissue
 
 16 Diseases of the genitourinary system
 
 17 Conditions related to sexual health
 
 18 Pregnancy, childbirth or the puerperium
 
 19 Certain conditions originating in the perinatal period
 
 20 Developmental anomalies
 
 21 Symptoms, signs or clinical findings, not elsewhere classified
 
 22 Injury, poisoning or certain other consequences of external causes

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Last updated: January 26, 2021
ICD-11 by World Health Organization

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