270.8 - Other Specified Disorders Of Amino-acid Metabolism
The ICD 9 Code for Other specified disorders of amino-acid metabolism is listed as 270.8.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | 270.8 |
| Long Description: | Other specified disorders of amino-acid metabolism |
| Short Description: | Dis amino-acid metab NEC |
| Chapter: | Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders |
| Block: | Other Metabolic Disorders And Immunity Disorders (270-279) |
| Related Descriptions: |
5-Oxoprolinase deficiency
Abnormal amino acid sequence Alaninemia Aminomethyltransferase deficiency Aromatic amino acid decarboxylase deficiency Beta-hydroxyisobutyryl-CoA deacylase deficiency Biotin-(propionyl-CoA-carboxylase) ligase deficiency Carnosinuria Cobalamin D disease D-2(OH) glutaric aciduria Disorder of amino acid and organic acid metabolism Disorder of aromatic amino acid metabolism Disorder of beta and omega amino acid metabolism Disorder of catecholamine synthesis Disorder of creatine synthesis Disorder of isoleucine metabolism Disorder of lysine and hydroxylysine metabolism Disorder of phenylalanine metabolism Disorder of proline AND/OR hydroxyproline metabolism Disorder of propionate AND/OR methylmalonate metabolism Disorder of tetrahydrobiopterin metabolism Disorder of the gamma-glutamyl cycle Disorder of valine metabolism Dopamine beta-hydroxylase deficiency Ethanolaminosis Familial renal iminoglycinuria gamma-Glutamyltransferase deficiency Glucoaminophosphaturia syndrome Glucoaminophosphaturia syndrome with rickets Glutamate formiminotransferase deficiency Glutamate-cysteine ligase deficiency Glutaric aciduria Glutathione synthase deficiency with 5-oxoprolinuria Glutathionemia Glycoprolinuria Hyper-beta-alaninemia Hyperdicarboxylicaminoaciduria AND hyperprolinemia Hyperhydroxyprolinemia Hyperprolinemia Iminoacidopathy Iminoglycinuria Inborn error of glutathione metabolism Lowe syndrome Lysinuric protein intolerance Ornithine oxo-acid aminotransferase deficiency Proline dehydrogenase deficiency Prolinuria Propionyl-CoA carboxylase deficiency pccA complementation group Propionyl-CoA carboxylase deficiency pccBC complementation group Sarcosine dehydrogenase deficiency Succinyl-CoA acetoacetate transferase deficiency |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | E72.03 - Lowe's syndrome (approximate) |
| ICD-10-CM Code: | E72.8 - Other specified disorders of amino-acid metabolism (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 270.8: | |
| 270.0 - Disturbances of amino-acid transport | |
| 270.1 - Phenylketonuria [PKU] | |
| 270.2 - Other disturbances of aromatic amino-acid metabolism | |
| 270.3 - Disturbances of branched-chain amino-acid metabolism | |
| 270.4 - Disturbances of sulphur-bearing amino-acid metabolism | |
| 270.5 - Disturbances of histidine metabolism | |
| 270.6 - Disorders of urea cycle metabolism | |
| 270.7 - Other disturbances of straight-chain amino-acid metabolism | |
| 270.9 - Unspecified disorder of amino-acid metabolism | |