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
       5C53  Inborn errors of energy metabolism
         H01427  Mitochondrial disease
         H01096  Pyruvate kinase deficiency
         H00072  Pyruvate dehydrogenase complex deficiency
         H01996  Pyruvate dehydrogenase phosphatase deficiency
         H01997  Pyruvate dehydrogenase E1-alpha deficiency
         H01998  Pyruvate dehydrogenase E1-beta deficiency
         H01999  Pyruvate dehydrogenase E2 deficiency
         H02000  Dihydrolipoamide dehydrogenase deficiency
         H02003  Pyruvate dehydrogenase E3-binding protein deficiency
         H00073  Pyruvate carboxylase deficiency
         H02197  Mitochondrial pyruvate carrier deficiency
         H02438  Hyperglycinemia, lactic acidosis, and seizures
         H01022  Diseases of the tricarboxylic acid cycle
         H02004  Fumarase deficiency
         H02006  Alpha-ketoglutarate dehydrogenase complex deficiency
         H02113  Infantile cerebellar-retinal degeneration
         H00469  Mitochondrial DNA depletion syndrome
         H01389  Alpers syndrome
         H01390  Mitochondrial neurogastrointestinal encephalomyopathy
         H01384  Mitochondrial recessive ataxia syndrome
         H00999  Coenzyme Q10 deficiency
         H00871  Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
         H01367  Infantile liver failure
         H01354  Leigh syndrome
         H01369  ATP synthase deficiency
         H00473  Mitochondrial complex I deficiency
         H00891  Combined oxidative phosphorylation deficiency
         H00920  Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis
         H01201  Jensen syndrome
         H01368  Cytochrome c oxidase (COX) deficiency
         H01894  Multiple mitochondrial dysfunctions syndrome
         H02005  Mitochondrial complex II deficiency
         H02007  GRACILE syndrome
         H02086  Mitochondrial complex III deficiency
         H01305  Global cerebral hypomyelination
         H01348  Mitochondrial phosphate carrier deficiency
         H00834  Guanidinoacetate methyltransferase deficiency
         H00849  Cerebral creatine deficiency syndrome
         H02181  Idiopathic hyperCKemia
         H02196  X-linked creatine deficiency syndrome
         H01248  Erythrocyte lactate transporter defect
         H01900  Encephalopathy due to defective mitochondrial and peroxisomal fission
       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 16, 2021
ICD-11 by World Health Organization

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