ICD-9 Diagnosis Code 277.89

Metabolism disorder NEC

Diagnosis Code 277.89

ICD-9: 277.89
Short Description: Metabolism disorder NEC
Long Description: Other specified disorders of metabolism
This is the 2014 version of the ICD-9-CM diagnosis code 277.89

Code Classification
  • Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279)
    • Other metabolic disorders and immunity disorders (270-279)
      • 277 Other and unspecified disorders of metabolism

Information for Medical Professionals

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  • Acatalasemia
  • Acatalasia
  • Adenosine deaminase overproduction
  • Alpha-N-acetylgalactosaminidase deficiency
  • Anemia due to disorders of nucleotide metabolism
  • Angioedema due to disorder of kinin metabolism
  • Autosomal variant form of transthyretin
  • Combined complex deficiencies
  • Combined deficiency of long chain 3-hydroxyacyl-coenzyme A dehydrogenase and enoyl-coenzyme A 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-coenzyme A dehydrogenase
  • Deficiency of limit dextrinase
  • Deficiency of protease
  • Deletion and duplication of mitochondrial deoxyribonucleic acid
  • Depletion of mitochondrial deoxyribonucleic acid
  • 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-Schüller-Christian disease
  • Histiocytosis X syndrome
  • Homocarnosinase deficiency
  • Hyper-beta-carnosinemia
  • Hyperimidodipeptiduria due to proline dipeptidase deficiency
  • Hypermanganesemia with dystonia, polycythemia, and cirrhosis
  • 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 deficiency
  • Polyostotic sclerosing histiocytosis
  • 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

Index of Diseases and Injuries
References found for the code 277.89 in the Index of Diseases and Injuries:

Information for Patients

Metabolic Disorders

Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues, such as your liver, muscles, and body fat.

A metabolic disorder occurs when abnormal chemical reactions in your body disrupt this process. When this happens, you might have too much of some substances or too little of other ones that you need to stay healthy.

You can develop a metabolic disorder when some organs, such as your liver or pancreas, become diseased or do not function normally. Diabetes is an example.

  • Acid mucopolysaccharides
  • Acidosis
  • Alkalosis
  • Homocystinuria
  • Lactic acid test
  • Metabolic acidosis
  • Metabolic neuropathies
  • Pseudohypoparathyroidism
  • Sanfilippo syndrome

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