2007 ICD-9-CM Diagnosis Code 277.89
Other specified disorders of metabolism
- Short description: METABOLISM DISORDER NEC.
- ICD-9-CM 277.89 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 277.89 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2007 version of ICD-9-CM 277.89.
- More recent version(s) of ICD-9-CM 277.89: 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
277.89 converts approximately to:
- 2015/16 ICD-10-CM C96.5 Multifocal and unisystemic Langerhans-cell histiocytosis
Or:
- 2015/16 ICD-10-CM C96.6 Unifocal Langerhans-cell histiocytosis
Or:
- 2015/16 ICD-10-CM E71.39 Other disorders of fatty-acid metabolism
Or:
- 2015/16 ICD-10-CM E80.3 Defects of catalase and peroxidase
Or:
- 2015/16 ICD-10-CM E88.89 Other specified metabolic disorders
Or:
- 2015/16 ICD-10-CM E88.9 Metabolic disorder, unspecified
Approximate Synonyms
- Acatalasemia
- Acatalasia
- Acatalasia (Takahara's disease)
- Acute histiocytosis
- Adenosine deaminase overproduction
- Alpha-N-acetylgalactosaminidase deficiency
- Anemia due to disorders of nucleotide metabolism
- Autosomal variant form of transthyretin
- Chronic histiocytosis
- 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 lysosomal enzyme
- 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-Schüller-Christian disease
- Hand-Sch�ller-Christian disease
- Histiocytic syndrome
- Histiocytosis
- Histiocytosis x
- Histiocytosis X syndrome
- Histiocytosis, acute
- Histiocytosis, chronic
- Histiocytosis, langerhans cell, unifocal
- Histiocytosis, undetermined cell
- Histiocytosis, unifocal langerhans-cell
- 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, disseminated (clinical)
- Langerhans cell histiocytosis, disseminated (disorder)
- Langerhans cell histiocytosis, multifoc unisystem
- Langerhans cell histiocytosis, multifocal and unisystemic
- Langerhans cell histiocytosis, unifocal
- Langerhans cell histiocytosis, unifocal (clinical)
- Lysosomal enzyme defect
- Lysosomal enzyme disorder
- Macroamylasemia
- Methylene THF reductase deficiency AND homocystinuria
- Mucinous histiocytosis of the colon
- Organic acid metabolism disorder
- Pancreatic colipase deficiency
- Pancreatic triacylglycerol lipase deficiency
- Phosphoenolpyruvate carboxykinase 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
- Unifocal langerhans-cell histiocytosis
Applies To
- Hand-Schüller-Christian disease
- Histiocytosis (acute) (chronic)
- Histiocytosis X (chronic)
Christian's (chronic histiocytosis X) 277.89
Schüller-Christian (chronic histiocytosis X) 277.89
