| ICD-10-CM-2023 > E00-E89 > E70-E88 > E72 |
E70-E88 | Metabolic disorders | |
Excl1.: | androgen insensitivity syndrome (E34.5-) congenital adrenal hyperplasia (E25.0) hemolytic anemias attributable to enzyme disorders (D55.-) Marfan's syndrome (Q87.4) 5-alpha-reductase deficiency (E29.1) | |
Excl2.: | Ehlers-Danlos syndromes (Q79.6-) | |
E72 | Other disorders of amino-acid metabolism | |
Excl1.: | disorders of: aromatic amino-acid metabolism (E70.-) branched-chain amino-acid metabolism (E71.0-E71.2) fatty-acid metabolism (E71.3) purine and pyrimidine metabolism (E79.-) gout (M1A.-, M10.-) | |
E72.0 | Disorders of amino-acid transport | |
Excl1.: | disorders of tryptophan metabolism (E70.5) | |
E72.00 | Disorders of amino-acid transport, unspecified | |
E72.01 | Cystinuria | |
E72.02 | Hartnup's disease | |
E72.03 | Lowe's syndrome | |
Use add'l | code for associated glaucoma (H42) | |
E72.04 | Cystinosis | |
Info: | Fanconi (-de Toni) (-Debré) syndrome with cystinosis | |
Excl1.: | Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09) | |
E72.09 | Other disorders of amino-acid transport | |
Info: | Fanconi (-de Toni) (-Debré) syndrome, unspecified | |
E72.1 | Disorders of sulfur-bearing amino-acid metabolism | |
Excl1.: | cystinosis (E72.04) cystinuria (E72.01) transcobalamin II deficiency (D51.2) | |
E72.10 | Disorders of sulfur-bearing amino-acid metabolism, unspecified | |
E72.11 | Homocystinuria | |
Info: | Cystathionine synthase deficiency | |
E72.12 | Methylenetetrahydrofolate reductase deficiency | |
E72.19 | Other disorders of sulfur-bearing amino-acid metabolism | |
Info: | Cystathioninuria Methioninemia Sulfite oxidase deficiency | |
E72.2 | Disorders of urea cycle metabolism | |
Excl1.: | disorders of ornithine metabolism (E72.4) | |
E72.20 | Disorder of urea cycle metabolism, unspecified | |
Info: | Hyperammonemia | |
Excl1.: | hyperammonemia-hyperornithinemia-homocitrullinemia syndrome E72.4 transient hyperammonemia of newborn (P74.6) | |
E72.21 | Argininemia | |
E72.22 | Arginosuccinic aciduria | |
E72.23 | Citrullinemia | |
E72.29 | Other disorders of urea cycle metabolism | |
E72.3 | Disorders of lysine and hydroxylysine metabolism | |
Info: | Glutaric aciduria NOS Glutaric aciduria (type I) Hydroxylysinemia Hyperlysinemia | |
Excl1.: | glutaric aciduria type II (E71.313) Refsum's disease (G60.1) Zellweger syndrome (E71.510) | |
E72.4 | Disorders of ornithine metabolism | |
Info: | Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome Ornithinemia (types I, II) Ornithine transcarbamylase deficiency | |
Excl1.: | hereditary choroidal dystrophy (H31.2-) | |
E72.5 | Disorders of glycine metabolism | |
E72.50 | Disorder of glycine metabolism, unspecified | |
E72.51 | Non-ketotic hyperglycinemia | |
E72.52 | Trimethylaminuria | |
E72.53 | Primary hyperoxaluria | |
Info: | Oxalosis Oxaluria | |
E72.59 | Other disorders of glycine metabolism | |
Info: | D-glycericacidemia Hyperhydroxyprolinemia Hyperprolinemia (types I, II) Sarcosinemia | |
E72.8 | Other specified disorders of amino-acid metabolism | |
E72.81 | Disorders of gamma aminobutyric acid metabolism | |
Info: | 4-hydroxybutyric aciduria Disorders of GABA metabolism GABA metabolic defect GABA transaminase deficiency GABA-T deficiency Gamma-hydroxybutyric aciduria SSADHD Succinic semialdehyde dehydrogenase deficiency | |
E72.89 | Other specified disorders of amino-acid metabolism | |
Info: | Disorders of beta-amino-acid metabolism Disorders of gamma-glutamyl cycle | |
E72.9 | Disorder of amino-acid metabolism, unspecified | |
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