Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
E72.0 Disorders of amino-acid transport Cystinosis Cystinuria Fanconi(-de Toni)(-Debré) syndrome Hartnup's disease Lowe's syndrome Excludes: disorders of tryptophan metabolism ( E70.8 ) E72.1 Disorders of sulfur-bearing amino-acid metabolism Cystathioninuria Homocystinuria Methioninaemia Sulfite oxidase deficiency Excludes: transcobalamin II deficiency ( D51.2 ) E72.2 Disorders of urea cycle metabolism Argininaemia Argininosuccinic aciduria Citrullinaemia Hyperammonaemia Excludes: disorders of ornithine metabolism ( E72.4 ) E72.3 Disorders of lysine and hydroxylysine metabolism Glutaric aciduria Hydroxylysinaemia Hyperlysinaemia Excludes: Refsum's disease ( G60.1 ) Zellweger's syndrome ( Q87.8 ) E72.4 Disorders of ornithine metabolism Ornithinaemia (types I, II) E72.5 Disorders of glycine metabolism Hyperhydroxyprolinaemia Hyperprolinaemia (types I, II) Non-ketotic hyperglycinaemia Sarcosinaemia E72.8 Other specified disorders of amino-acid metabolism Disorders of: · Beta-amino-acid metabolism · Gamma-glutamyl cycle E72.9 Disorder of amino-acid metabolism, unspecified E73 Lactose intolerance E73.0 Congenital lactase deficiency E73.1 Secondary lactase deficiency E73.8 Other lactose intolerance E73.9 Lactose intolerance, unspecified 160 WHO’s ICD-10
E74 Other disorders of carbohydrate metabolism Excludes: increased secretion of glucagon ( E16.3 ) diabetes mellitus ( E10-E14 ) hypoglycaemia NOS ( E16.2 ) mucopolysaccharidosis ( E76.0-E76.3 ) E74.0 Glycogen storage disease Cardiac glycogenosis Disease: · Andersen · Cori · Forbes · Hers · McArdle · Pompe · Tauri · von Gierke Liver phosphorylase deficiency E74.1 Disorders of fructose metabolism Essential fructosuria Fructose-1,6-diphosphatase deficiency Hereditary fructose intolerance E74.2 Disorders of galactose metabolism Galactokinase deficiency Galactosaemia E74.3 Other disorders of intestinal carbohydrate absorption Glucose-galactose malabsorption Sucrase deficiency Excludes: lactose intolerance ( E73.- ) E74.4 Disorders of pyruvate metabolism and gluconeogenesis Deficiency of: · phosphoenolpyruvate carboxykinase · pyruvate: · carboxylase · dehydrogenase Excludes: with anaemia ( D55.- ) E74.8 Other specified disorders of carbohydrate metabolism Essential pentosuria Oxalosis Oxaluria Renal glycosuria E74.9 Disorder of carbohydrate metabolism, unspecified Version for 2007 161
- Page 109 and 110: D10.4 Tonsil Tonsil (faucial)(palat
- Page 111 and 112: D14 Benign neoplasm of middle ear a
- Page 113 and 114: D19.7 Mesothelial tissue of other s
- Page 115 and 116: D23.0 Skin of lip Excludes: vermili
- Page 117 and 118: D30.7 Other urinary organs Parauret
- Page 119 and 120: Neoplasms of uncertain or unknown b
- Page 121 and 122: D40 Neoplasm of uncertain or unknow
- Page 123 and 124: D47.2 Monoclonal gammopathy D47.3 E
- Page 125 and 126: Chapter III Diseases of the blood a
- Page 127 and 128: D53.9 Nutritional anaemia, unspecif
- Page 129 and 130: D59 Acquired haemolytic anaemia D59
- Page 131 and 132: D64.0 Hereditary sideroblastic anae
- Page 133 and 134: Use additional external cause code
- Page 135 and 136: D72.1 Eosinophilia Eosinophilia: ·
- Page 137 and 138: D76.0 Langerhans' cell histiocytosi
- Page 139 and 140: D84 Other immunodeficiencies D84.0
- Page 141 and 142: E00.1 Congenital iodine-deficiency
- Page 143 and 144: E06 Thyroiditis Excludes: postpartu
- Page 145 and 146: E10 E11 E12 Insulin-dependent diabe
- Page 147 and 148: E16.2 Hypoglycaemia, unspecified E1
- Page 149 and 150: E23.2 Diabetes insipidus Excludes:
- Page 151 and 152: E28.1 Androgen excess Hypersecretio
- Page 153 and 154: · nutritional ( E45 ) · pituitary
- Page 155 and 156: Other nutritional deficiencies (E50
- Page 157 and 158: E59 E60 Dietary selenium deficiency
- Page 159: E70.1 Other hyperphenylalaninaemias
- Page 163 and 164: E76 Disorders of glycosaminoglycan
- Page 165 and 166: E80 Disorders of porphyrin and bili
- Page 167 and 168: E86 Volume depletion Dehydration De
- Page 169 and 170: Chapter V Mental and behavioural di
- Page 171 and 172: F02* Dementia in other diseases cla
- Page 173 and 174: F05.8 Other delirium Delirium of mi
- Page 175 and 176: F07 Personality and behavioural dis
- Page 177 and 178: Psychoactive substance abuse .2 Dep
- Page 179 and 180: F15 F16 F17 F18 F19 Mental and beha
- Page 181 and 182: F20.4 Post-schizophrenic depression
- Page 183 and 184: F23 Acute and transient psychotic d
- Page 185 and 186: F25.2 Schizoaffective disorder, mix
- Page 187 and 188: F31.3 Bipolar affective disorder, c
- Page 189 and 190: Includes: recurrent episodes of: ·
- Page 191 and 192: mad. Contemplating entry to the pho
- Page 193 and 194: ecognized as his or her own thought
- Page 195 and 196: epresented a major developmental tr
- Page 197 and 198: limb or limbs. There may be close r
- Page 199 and 200: Cardiac neurosis Da Costa's syndrom
- Page 201 and 202: Behavioural syndromes associated wi
- Page 203 and 204: Excludes: hypersomnia (organic) ( G
- Page 205 and 206: F53 Mental and behavioural disorder
- Page 207 and 208: Personality (disorder): · expansiv
- Page 209 and 210: F60.8 Other specific personality di
E72.0 Disorders of amino-acid transport<br />
Cystinosis<br />
Cystinuria<br />
Fanconi(-de Toni)(-Debré) syndrome<br />
Hartnup's disease<br />
Lowe's syndrome<br />
Excludes: disorders of tryptophan metabolism ( E70.8 )<br />
E72.1 Disorders of sulfur-bearing amino-acid metabolism<br />
Cystathioninuria<br />
Homocystinuria<br />
Methioninaemia<br />
Sulfite oxidase deficiency<br />
Excludes: transcobalamin II deficiency ( D51.2 )<br />
E72.2 Disorders of urea cycle metabolism<br />
Argininaemia<br />
Argininosuccinic aciduria<br />
Citrullinaemia<br />
Hyperammonaemia<br />
Excludes: disorders of ornithine metabolism ( E72.4 )<br />
E72.3 Disorders of lysine <strong>and</strong> hydroxylysine metabolism<br />
Glutaric aciduria<br />
Hydroxylysinaemia<br />
Hyperlysinaemia<br />
Excludes: Refsum's disease ( G60.1 )<br />
Zellweger's syndrome ( Q87.8 )<br />
E72.4 Disorders of ornithine metabolism<br />
Ornithinaemia (types I, II)<br />
E72.5 Disorders of glycine metabolism<br />
Hyperhydroxyprolinaemia<br />
Hyperprolinaemia (types I, II)<br />
Non-ketotic hyperglycinaemia<br />
Sarcosinaemia<br />
E72.8 Other specified disorders of amino-acid metabolism<br />
Disorders of:<br />
· Beta-amino-acid metabolism<br />
· Gamma-glutamyl cycle<br />
E72.9 Disorder of amino-acid metabolism, unspecified<br />
E73 Lactose intolerance<br />
E73.0 Congenital lactase deficiency<br />
E73.1 Secondary lactase deficiency<br />
E73.8 Other lactose intolerance<br />
E73.9 Lactose intolerance, unspecified<br />
160 WHO’s ICD-10
Change language