277.89 - Other Specified Disorders Of Metabolism
The ICD 9 Code for Other specified disorders of metabolism is listed as 277.89.
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: | 277.89 |
| Long Description: | Other specified disorders of metabolism |
| Short Description: | Metabolism disorder NEC |
| Chapter: | Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders |
| Block: | Other Metabolic Disorders And Immunity Disorders (270-279) |
| Related Descriptions: |
Acatalasemia
Acatalasia Adenosine deaminase overproduction Alpha-N-acetylgalactosaminidase deficiency Anemia due to disorders of nucleotide metabolism Autosomal variant form of transthyretin Combined complex deficiencies Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase Defect in post-translational modification of lysosomal enzymes Defective biosynthesis Defective osmoregulation Deficiency in enzyme complexes of mitochondrial respiratory chain Deficiency of amylopectin 6-glucanohydrolase Deficiency of glycosidase Deficiency of halogenase Deficiency of isobutyryl-CoA dehydrogenase Deficiency of limit dextrinase Deficiency of protease Deletion and duplication of mitochondrial DNA Depletion of mitochondrial DNA Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism Disorder of chromium metabolism Disorder of glucose regulation Disorder of glycoprotein metabolism Disorder of glycosaminoglycan metabolism Disorder of iodine metabolism Disorder of mitochondrial respiratory chain complexes Disorder of organic acid metabolism Disorder of osmoregulation Disorder of oxygen transport Disorder of peroxisomal function Disorder of protein metabolism Disorder of pyruvate metabolism and mitochondrial respiratory chain Disorder of sialic acid metabolism Disorder of steroid metabolism Disorder of strontium metabolism Disorder with defective osteoid mineralization Disorders of pyruvate metabolism and gluconeogenesis Drug resistance to insulin Enterokinase deficiency Eosinophilic granuloma of bone Extensive metabolizer due to cytochrome p450 CYP2D6 variant Familial sea-blue histiocytosis Fast acetylator due to N-acetyltransferase enzyme variant Fat overload syndrome Glutaric aciduria, type 1 Glutathione S-transferase deficiency Hand-Sch Histiocytosis X syndrome Homocarnosinase deficiency Hyper-beta-carnosinemia Hyperimidodipeptiduria due to proline dipeptidase deficiency Impaired oxygen extraction Inborn error of pyruvate metabolism Increased auto-oxidation Increased fluid pressure Increased oxygen demand Inherited metabolic disorder of nervous system Intermediate metabolizer due to cytochrome p450 CYP2D6 variant Langerhans cell histiocytosis Langerhans cell histiocytosis - Hashimoto-Pritzker type Langerhans cell histiocytosis of lung Langerhans cell histiocytosis, unifocal Macroamylasemia Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria Mucinous histiocytosis of the colon Pancreatic colipase deficiency Pancreatic triacylglycerol lipase deficiency Phosphoenolpyruvate carboxykinase (GTP) deficiency Poor metabolizer due to cytochrome p450 CYP2C19 variant Poor metabolizer due to cytochrome p450 CYP2C9 variant Poor metabolizer due to cytochrome p450 CYP2D6 variant Pseudoinfantile Refsum's disease Pyruvate carboxylase deficiency Pyruvate dehydrogenase complex deficiency Refeeding syndrome Sepiapterin reductase deficiency Sinus histiocytosis with massive lymphadenopathy Slow acetylator due to N-acetyltransferase enzyme variant Solitary reticulohistiocytoma Tetrahydrobiopterin synthesis defect Trypsinogen deficiency Tumor lysis syndrome UGT1A1*28 polymorphism Ultrarapid metabolizer due to cytochrome p450 CYP2D6 variant Undetermined cell histiocytosis |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | C96.5 - Multifocal and unisystemic Langerhans-cell histiocytosis (approximate) |
| ICD-10-CM Code: | C96.6 - Unifocal Langerhans-cell histiocytosis (approximate) |
| ICD-10-CM Code: | E71.39 - Other disorders of fatty-acid metabolism (approximate) |
| ICD-10-CM Code: | E80.3 - Defects of catalase and peroxidase (approximate) |
| ICD-10-CM Code: | E88.89 - Other specified metabolic disorders (approximate) |
| ICD-10-CM Code: | E88.9 - Metabolic disorder, unspecified (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 277.89: | |
| 277.81 - Primary carnitine deficiency | |
| 277.82 - Carnitine deficiency due to inborn errors of metabolism | |
| 277.83 - Iatrogenic carnitine deficiency | |
| 277.84 - Other secondary carnitine deficiency | |
| 277.85 - Disorders of fatty acid oxidation | |
| 277.86 - Peroxisomal disorders | |
| 277.87 - Disorders of mitochondrial metabolism | |
| 277.88 - Tumor lysis syndrome | |