| 01 Certain infectious or parasitic diseases (95) |
| 1E51.1 Chronic hepatitis C (91) |
| 1E5Z Viral hepatitis, unspecified (4) |
| 02 Neoplasms (704) |
| 02 Neoplasms (312) |
| 2A00.5 Primary neoplasm of brain of unknown or unspecified type (85) |
| 2A20.4 Polycythaemia vera (7) |
| 2A60.Z Acute myeloid leukaemias and related precursor neoplasms, unspecified (51) |
| 2A7Z Precursor lymphoid neoplasms, unspecified (4) |
| 2A82.0Z Chronic lymphocytic leukaemia or small lymphocytic lymphoma, unspecified (1) |
| 2A83.1 Plasma cell myeloma (4) |
| 2B31.Z Histiocytic or dendritic cell neoplasms, unspecified (56) |
| 2B33.4 Leukaemia, unspecified (3) |
| 2B3Z Neoplasms of haematopoietic or lymphoid tissues, unspecified (78) |
| 2B5Z Malignant mesenchymal neoplasm of unspecified type (26) |
| 2B90.Z Malignant neoplasms of colon, unspecified (16) |
| 2C23.Z Malignant neoplasms of larynx, unspecified (4) |
| 2C25.Z Malignant neoplasms of bronchus or lung, unspecified (28) |
| 2C73.Z Malignant neoplasms of ovary, unspecified (1) |
| 2C82.Z Malignant neoplasms of prostate, unspecified (1) |
| 2D02.Z Malignant neoplasm of retina, unspecified (9) |
| 2D12.Z Malignant neoplasms of other endocrine glands or related structures, unspecified (18) |
| 03 Diseases of the blood or blood-forming organs (192) |
| 3A10.00 Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency (1) |
| 3A21 Acquired haemolytic anaemia, non-immune (9) |
| 3A21.0 Paroxysmal nocturnal haemoglobinuria (1) |
| 3A50.0Z Alpha thalassaemia, unspecified (9) |
| 3A50.2 Beta thalassaemia (14) |
| 3A50.Z Thalassaemias, unspecified (72) |
| 3A51.1 Sickle cell disease without crisis (48) |
| 3A70.12 Idiopathic aplastic anaemia (3) |
| 3A9Z Anaemias or other erythrocyte disorders, unspecified (8) |
| 3B10.Z Hereditary factor VIII deficiency, unspecified (7) |
| 3B11.Z Hereditary factor IX deficiency, unspecified (1) |
| 3B62.Z Qualitative platelet defects, unspecified (4) |
| 3B64.10 Immune thrombocytopenic purpura (7) |
| 3B64.Z Thrombocytopenia, unspecified (8) |
| 04 Diseases of the immune system (393) |
| 4A00.0Z Functional neutrophil defects, unspecified (15) |
| 4A01.0Z Immunodeficiencies with predominantly antibody defects, unspecified (10) |
| 4A01.10 Severe combined immunodeficiencies (35) |
| 4A01.34 Hyperimmunoglobulin E syndromes (3) |
| 4A0Z Primary immunodeficiencies, unspecified (42) |
| 4A40.0Z Systemic lupus erythematosus, unspecified (24) |
| 4A41.20 Inflammatory inclusion body myositis (4) |
| 4A41.Z Idiopathic inflammatory myopathy, unspecified (14) |
| 4A42.1 Diffuse systemic sclerosis (3) |
| 4A42.Z Systemic sclerosis, unspecified (68) |
| 4A44.8 Thromboangiitis obliterans (1) |
| 4A44.A2 Eosinophilic granulomatosis with polyangiitis (4) |
| 4A4Z Nonorgan specific systemic autoimmune disorders, unspecified (70) |
| 4A62 Beh?et disease (3) |
| 4B00 Disorders of neutrophil number (4) |
| 4B0Z Immune system disorders involving white cell lineages, unspecified (5) |
| 4B20.Z Sarcoidosis, unspecified (4) |
| 4B4Z Diseases of the immune system, unspecified (84) |
| 05 Endocrine, nutritional or metabolic diseases (3869) |
| 5A00.02 Pendred syndrome (19) |
| 5A00.Z Hypothyroidism, unspecified (20) |
| 5A10 Type 1 diabetes mellitus (855) |
| 5A11 Type 2 diabetes mellitus (1990) |
| 5A13 Diabetes mellitus, other specified type (460) |
| 5A50.Z Hypoparathyroidism, unspecified (3) |
| 5A5Z Disorders of the parathyroids or parathyroid hormone system, unspecified (5) |
| 5A61.0 Hypopituitarism (3) |
| 5A61.5 Central diabetes insipidus (3) |
| 5A71.01 Congenital adrenal hyperplasia (4) |
| 5A80.1 Polycystic ovary syndrome (1) |
| 5B3Z Endocrine diseases, unspecified (212) |
| 5C50.00 Classical phenylketonuria (3) |
| 5C50.1Z Disorders of tyrosine metabolism, unspecified (2) |
| 5C50.4 Disorders of lysine or hydroxylysine metabolism (1) |
| 5C50.7Z Disorders of glycine metabolism, unspecified (1) |
| 5C50.9 Disorders of ornithine metabolism (6) |
| 5C51.3 Glycogen storage disease (28) |
| 5C52.0Z Inborn errors of fatty acid oxidation or ketone body metabolism, unspecified (10) |
| 5C53.0Z Disorders of pyruvate metabolism, unspecified (5) |
| 5C55.01 Lesch-Nyhan syndrome (2) |
| 5C56.00 Gangliosidosis (40) |
| 5C56.1 Neuronal ceroid lipofuscinosis (17) |
| 5C56.2Z Glycoproteinosis, unspecified (9) |
| 5C56.30 Mucopolysaccharidosis type 1 (1) |
| 5C56.31 Mucopolysaccharidosis type 2 (11) |
| 5C56.3Z Mucopolysaccharidosis, unspecified (15) |
| 5C56.4 Disorders of sialic acid metabolism (8) |
| 5C58.00 Crigler-Najjar syndrome (4) |
| 5C58.01 Gilbert syndrome (1) |
| 5C64.0Z Disorders of copper metabolism, unspecified (16) |
| 5C64.10 Iron overload diseases (5) |
| 5C64.3 Disorders of phosphorus metabolism or phosphatases (7) |
| 5C80.00 Primary hypercholesterolaemia (8) |
| 5C80.1 Hypertriglyceridaemia (6) |
| 5C80.Z Hyperlipoproteinaemia, unspecified (2) |
| 5D00.0 AL amyloidosis (5) |
| 5D00.1 AA amyloidosis (1) |
| 5D00.20 Hereditary ATTR amyloidosis (19) |
| 5D00.21 Non-neuropathic heredofamilial amyloidosis (9) |
| 5D00.Z Amyloidosis, unspecified (3) |
| 5D2Z Metabolic disorders, unspecified (49) |
| 06 Mental, behavioural or neurodevelopmental disorders (659) |
| 6A00.0 Disorder of intellectual development, mild (4) |
| 6A00.1 Disorder of intellectual development, moderate (4) |
| 6A00.2 Disorder of intellectual development, severe (4) |
| 6A00.3 Disorder of intellectual development, profound (4) |
| 6A00.Z Disorders of intellectual development, unspecified (32) |
| 6A02.Z Autism spectrum disorder, unspecified (57) |
| 6A05.Z Attention deficit hyperactivity disorder, presentation unspecified (24) |
| 6A0Z Neurodevelopmental disorders, unspecified (42) |
| 6A20.Z Schizophrenia, episode unspecified (352) |
| 6A6Z Bipolar or related disorders, unspecified (78) |
| 6A70.Z Single episode depressive disorder, unspecified (5) |
| 6A71.1 Recurrent depressive disorder, current episode moderate, without psychotic symptoms (3) |
| 6A71.3 Recurrent depressive disorder, current episode severe, without psychotic symptoms (1) |
| 6A71.Z Recurrent depressive disorder, unspecified (15) |
| 6B20.Z Obsessive-compulsive disorder, unspecified (20) |
| 6D80.Z Dementia due to Alzheimer disease, onset unknown or unspecified (6) |
| 6D81 Dementia due to cerebrovascular disease (2) |
| 6D8Z Dementia, unknown or unspecified cause (6) |
| 07 Sleep-wake disorders (2) |
| 7A4Z Sleep-related breathing disorders, unspecified (2) |
| 08 Diseases of the nervous system (2756) |
| 8A00.0Z Parkinson disease, unspecified (370) |
| 8A00.10 Progressive supranuclear palsy (3) |
| 8A00.1Z Atypical parkinsonism, unspecified (75) |
| 8A01.10 Huntington disease (103) |
| 8A02.0Z Primary dystonia, unspecified (28) |
| 8A03.Z Ataxic disorders, unspecified (370) |
| 8A05.00 Tourette syndrome (1) |
| 8A20 Alzheimer disease (564) |
| 8A2Z Disorders with neurocognitive impairment as a major feature, unspecified (4) |
| 8A40.Z Multiple sclerosis, unspecified (51) |
| 8A45.01 Subacute sclerosing panencephalitis (1) |
| 8A45.02 Progressive multifocal leukoencephalopathy (1) |
| 8A61.Z Genetic or presumed genetic syndromes primarily expressed as epilepsy, unspecified (58) |
| 8A6Z Epilepsy or seizures, unspecified (85) |
| 8A80.Z Migraine, unspecified (48) |
| 8B11.5Z Cerebral ischaemic stroke, unspecified (2) |
| 8B22 Certain specified cerebrovascular diseases (7) |
| 8B22.B Moyamoya syndrome (16) |
| 8B44.0Z Hereditary spastic paraplegia, unspecified (37) |
| 8B60.Z Motor neuron disease, unspecified (147) |
| 8B61.0 Infantile spinal muscular atrophy, Type I (5) |
| 8B61.Z Spinal muscular atrophy, unspecified (112) |
| 8C01.0 Acute inflammatory demyelinating polyneuropathy (1) |
| 8C20.Z Hereditary motor or sensory neuropathy, unspecified (32) |
| 8C21.1 Hereditary sensory and autonomic neuropathy type III (1) |
| 8C4Z Disorders of nerve root, plexus or peripheral nerves, unspecified (120) |
| 8C60.Z Myasthenia gravis, unspecified (1) |
| 8C61 Congenital myasthenic syndromes (6) |
| 8C70.Z Muscular dystrophy, unspecified (125) |
| 8C71.Z Myotonic disorders, unspecified (27) |
| 8C72.Z Congenital myopathies, unspecified (19) |
| 8C73.Z Mitochondrial myopathies, unspecified (5) |
| 8C8Z Secondary myopathies, unspecified (6) |
| 8D20.11 Spastic diplegic cerebral palsy (1) |
| 8E4Z Other disorders of the nervous system, unspecified (324) |
| 09 Diseases of the visual system (328) |
| 9A70.Z Hereditary corneal dystrophies, unspecified (2) |
| 9B10.0Z Age-related cataract, unspecified (6) |
| 9B10.2 Certain specified cataracts (5) |
| 9B61 Choroidal dystrophy (1) |
| 9B70 Inherited retinal dystrophies (146) |
| 9B73.2 Retinal cysts (2) |
| 9B73.4 Retinal breaks without detachment (3) |
| 9B76 Degenerative high myopia (2) |
| 9B78.1Z Background retinopathy and retinal vascular changes, unspecified (1) |
| 9B78.3Z Degeneration of macula or posterior pole, unspecified (132) |
| 9B83 Vitreous haemorrhage (1) |
| 9C40.BZ Optic atrophy, unspecified (14) |
| 9C61.0Z Primary open-angle glaucoma, unspecified (9) |
| 9C61.4Z Developmental glaucoma, unspecified (2) |
| 9D44 Impairment of colour vision (2) |
| 10 Diseases of the ear or mastoid process (30) |
| AB31.0 Meniere disease (1) |
| AB33 Otosclerosis (12) |
| AB51.1 Acquired sensorineural hearing loss (12) |
| AB51.Z Acquired hearing impairment, unspecified (5) |
| 11 Diseases of the circulatory system (2166) |
| BA00.Z Essential hypertension, unspecified (2) |
| BB01.Z Pulmonary hypertension, unspecified (10) |
| BB0Z Pulmonary heart disease or diseases of pulmonary circulation, unspecified (44) |
| BB6Z Mitral valve disease, unspecified (6) |
| BC43.0Z Dilated cardiomyopathy, unspecified (339) |
| BC43.12 Obstructive hypertrophic cardiomyopathy (149) |
| BC43.1Z Hypertrophic cardiomyopathy, unspecified (154) |
| BC43.4 Cardiomyopathy due to drugs or other external agents (1) |
| BC43.Z Cardiomyopathy, unspecified (420) |
| BC4Z Diseases of the myocardium or cardiac chambers, unspecified (5) |
| BC63.2Z Complete atrioventricular block, unspecified (2) |
| BC63.4Z Left bundle branch block, fascicle unspecified (1) |
| BC63.Z Conduction disorders, unspecified (970) |
| BC71.0Z Ventricular tachycardia, unspecified (31) |
| BC80.20 Sick sinus syndrome (5) |
| BC81.30 Paroxysmal atrial fibrillation (2) |
| BC81.Z Supraventricular tachyarrhythmia, unspecified (3) |
| BD1Z Heart failure, unspecified (8) |
| BD50.3Z Thoracic aortic aneurysm, unspecified (4) |
| BD50.Z Aortic aneurysm or dissection, unspecified (8) |
| BD51.0 Aneurysm or dissection of carotid artery (1) |
| BD51.2 Aneurysm or dissection of other precerebral arteries (1) |
| 12 Diseases of the respiratory system (131) |
| CA08.00 Allergic rhinitis due to pollen (1) |
| CA22.Z Chronic obstructive pulmonary disease, unspecified (6) |
| CA25.Z Cystic fibrosis, unspecified (124) |
| 13 Diseases of the digestive system (23) |
| DB94.3 Alcoholic cirrhosis of liver without hepatitis (6) |
| DB95.2Z Drug-induced or toxic liver disease with cholestasis, unspecified (2) |
| DB96.0 Autoimmune hepatitis (2) |
| DC11.4 Calculus of bile duct with cholangitis (1) |
| DC1Z Diseases of gallbladder or biliary tract, unspecified (4) |
| DD71.3 Ulcerative proctitis (2) |
| DD71.Z Ulcerative colitis, unspecified (6) |
| 14 Diseases of the skin (92) |
| EA90.40 Generalised pustular psoriasis (1) |
| EA90.Z Psoriasis of unspecified type (42) |
| EB13.0 Stevens-Johnson syndrome (1) |
| EB21 Pyoderma gangrenosum (2) |
| EB40.1 Pemphigus foliaceus (3) |
| EB40.Z Pemphigus, unspecified (8) |
| EC23.0 Non-syndromic genetically-determined hypermelanosis or lentiginosis (1) |
| EC30 Epidermolysis bullosa simplex (12) |
| EC32 Dystrophic epidermolysis bullosa (10) |
| EC3Z Epidermolysis bullosa (6) |
| ED70.1 Female pattern hair loss (3) |
| ED80.Z Acne, unspecified (3) |
| 15 Diseases of the musculoskeletal system or connective tissue (61) |
| FA10.Z Direct infections of joint, unspecified (2) |
| FA20.Z Rheumatoid arthritis, serology unspecified (28) |
| FA23 Adult-onset Still disease (1) |
| FA31.7 Acquired clawfoot or clubfoot (3) |
| FA92.0Z Axial spondyloarthritis, unspecified (5) |
| FB31.1 Fibrodysplasia ossificans progressiva (21) |
| FB82.3 Relapsing polychondritis (1) |
| 16 Diseases of the genitourinary system (494) |
| GA30.6 Premature ovarian failure (7) |
| GA31.Z Female infertility without specification whether primary or secondary (4) |
| GB04.Z Male infertility, unspecified (1) |
| GB40 Nephritic syndrome (58) |
| GB41 Nephrotic syndrome (319) |
| GB4Z Glomerular diseases, unspecified (20) |
| GB5Z Renal tubulo-interstitial diseases, unspecified (18) |
| GB61.Z Chronic kidney disease, stage unspecified (3) |
| GB81 Autosomal dominant polycystic kidney disease (34) |
| GB82 Autosomal dominant tubulointerstitial disease (10) |
| GB8Z Cystic or dysplastic kidney disease, unspecified (20) |
| 18 Pregnancy, childbirth or the puerperium (4) |
| JB44.3 Cardiomyopathy in the puerperium (4) |
| 19 Certain conditions originating in the perinatal period (15) |
| KA40.Z Birth injury to central nervous system, unspecified (5) |
| KA89.Z Transient neonatal thrombocytopaenia, unspecified (1) |
| KB03 Neonatal encephalopathy (6) |
| KB60.2Z Neonatal diabetes mellitus, unspecified (3) |
| 20 Developmental anomalies (712) |
| LA02.Z Spina bifida, unspecified (9) |
| LA05.0 Microcephaly (3) |
| LA05.1 Megalencephaly (1) |
| LA05.3 Corpus callosum agenesis (4) |
| LA05.7 Brain cystic malformations (1) |
| LA11.3 Aniridia (3) |
| LA12.Z Structural developmental anomalies of lens or zonula, unspecified (4) |
| LA13.7Z Congenital malformation of optic disc, unspecified (2) |
| LA7Z Structural developmental anomalies of the respiratory system, unspecified (4) |
| LA86.20 Total anomalous pulmonary venous connection (1) |
| LA88.2Z Tetralogy of Fallot, unspecified (1) |
| LA89.3 Hypoplastic left heart syndrome (10) |
| LA8A.1Z Congenital pulmonary atresia, unspecified (2) |
| LA8Z Structural developmental anomaly of heart or great vessels, unspecified (15) |
| LA90.00 Hereditary haemorrhagic telangiectasia (6) |
| LA90.42 Congenital cerebral nonruptured aneurysm (1) |
| LA9Z Structural developmental anomalies of the circulatory system, unspecified (4) |
| LB16.1 Hirschsprung disease (3) |
| LB1Z Structural developmental anomalies of the digestive tract, unspecified (19) |
| LB20.Z Structural developmental anomalies of gallbladder, bile ducts or liver, unspecified (16) |
| LB70.0Z Craniosynostosis, unspecified (4) |
| LB78.Z Polydactyly, unspecified (2) |
| LB9Z Structural developmental anomalies of the skeleton, unspecified (42) |
| LC52 Complex or combined developmental vascular malformations involving the skin (1) |
| LD0Z Structural developmental anomalies primarily affecting one body system, unspecified (13) |
| LD24.02 Thanatophoric dysplasia (4) |
| LD24.10 Osteopetrosis (4) |
| LD24.1Z Bone diseases with increased bone density, unspecified (1) |
| LD24.20 Multiple osteochondromas (2) |
| LD24.3 Spondyloepiphyseal or spondyloepimetaphyseal dysplasias (6) |
| LD24.BZ Short rib syndromes, unspecified (1) |
| LD24.K0 Osteogenesis imperfecta (7) |
| LD24.Z Syndromes with skeletal anomalies as a major feature, unspecified (12) |
| LD27.02 Hypohidrotic ectodermal dysplasia (3) |
| LD27.1 Xeroderma pigmentosum (3) |
| LD27.2 Syndromic ichthyosis (3) |
| LD28.01 Marfan syndrome (14) |
| LD2A.4 46,XY disorder of sex development due to androgen resistance (3) |
| LD2C Overgrowth syndromes (4) |
| LD2D.10 Neurofibromatosis type 1 (10) |
| LD2D.2 Tuberous sclerosis (16) |
| LD40.0 Complete trisomy 21 (80) |
| LD42.Z Polyploidies, unspecified (1) |
| LD44.0 Chromosome replaced with ring or dicentric with normal number of chromosomes (14) |
| LD44.41 Deletions of the short arm of chromosome 4 (3) |
| LD44.51 Deletions of the short arm of chromosome 5 (1) |
| LD44.N0 CATCH 22 phenotype (10) |
| LD50.0 Turner syndrome (6) |
| LD50.1 Karyotype 47,XXX (1) |
| LD55 Fragile X chromosome (12) |
| LD7Z Chromosomal anomalies, excluding gene mutations, unspecified (204) |
| LD90.4 Rett syndrome (25) |
| LD9Z Developmental anomalies, unspecified (91) |
| 21 Symptoms, signs or clinical findings, not elsewhere classified (49) |
| MA18.00 Abnormal glucose tolerance test (1) |
| MB4B.1 Agnosia (2) |
| MC81.1 Bradycardia, unspecified (1) |
| MC91 Results of function studies of the circulatory system (7) |
| MF8Z Clinical findings in specimens from the urinary system, unspecified (38) |
| 22 Injury, poisoning or certain other consequences of external causes (151) |
| NE60 Harmful effects of drugs, medicaments or biological substances, not elsewhere classified (151) |
| 24 Factors influencing health status or contact with health services (3) |
| QA0A.4 Special screening examination for certain developmental disorders in childhood (3) |