ICD-10 Diagnosis Code E88.89

Other specified metabolic disorders

Diagnosis Code E88.89

ICD-10: E88.89
Short Description: Other specified metabolic disorders
Long Description: Other specified metabolic disorders
This is the 2017 version of the ICD-10-CM diagnosis code E88.89

Valid for Submission
The code E88.89 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Endocrine, nutritional and metabolic diseases (E00–E90)
    • Metabolic disorders (E70-E88)
      • Other and unspecified metabolic disorders (E88)

Information for Medical Professionals

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Synonyms
  • Adenosine deaminase overproduction
  • Angioedema due to disorder of kinin metabolism
  • Aromatase excess syndrome
  • Arylsulfatase deficiency without metachromatic leukodystrophy
  • Benign symmetric lipomatosis
  • Cerebral folate transport deficiency
  • Circulating enzyme deficiency
  • Clinical manifestation of enzyme deficiency
  • Complete deficiency of methylmalonyl-coenzyme A mutase
  • Congenital defect of folate absorption
  • Corticosteroid 11-reductase deficiency
  • Cytochrome p450 CYP1A2 enzyme deficiency
  • Cytochrome p450 CYP2C19 enzyme deficiency
  • Cytochrome p450 CYP2C9 enzyme deficiency
  • Cytochrome p450 CYP2D6 enzyme deficiency
  • Cytochrome p450 CYP2E1 enzyme deficiency
  • Cytochrome p450 CYP3A enzyme deficiency
  • Cytochrome p450 enzyme deficiency
  • Cytosolic acetoacetyl-coenzyme A thiolase deficiency
  • Deficiency of
  • Deficiency of
  • Deficiency of 1,3-beta-glucan synthase
  • Deficiency of 1,4-alpha-glucan 6alpha-glucosyltransferase
  • Deficiency of 1,4-alpha-glucan branching enzyme
  • Deficiency of 2,5-diaminovalerate aminotransferase
  • Deficiency of 3alpha-hydroxycholanate dehydrogenase
  • Deficiency of 3-mercaptopyruvate sulfurtransferase
  • Deficiency of 3-oxoacid coenzyme A-transferase
  • Deficiency of 3-oxoadipate coenzyme A-transferase
  • Deficiency of acetate kinase
  • Deficiency of acetylcholinesterase
  • Deficiency of acetyl-coenzyme A acetyltransferase
  • Deficiency of acetyl-coenzyme A acetyltransferase
  • Deficiency of acetylesterase
  • Deficiency of acid-ammonia ligase
  • Deficiency of aconitate hydratase
  • Deficiency of adenosine diphosphate deaminase
  • Deficiency of adenosine kinase
  • Deficiency of adenosine triphosphate pyrophosphatase
  • Deficiency of adenosinetriphosphatase
  • Deficiency of adenylate kinase
  • Deficiency of adenylylsulfate kinase
  • Deficiency of alcohol sulfotransferase
  • Deficiency of aldehyde dehydrogenase
  • Deficiency of aldehyde oxidase
  • Deficiency of aldehyde-lyase
  • Deficiency of alkaline phosphatase
  • Deficiency of alkaline phosphomonoesterase
  • Deficiency of alkylhalidase
  • Deficiency of alpha- and beta-trypsin
  • Deficiency of alpha-1,4-glucan-protein synthase
  • Deficiency of alpha-aminoacylpeptide hydrolase
  • Deficiency of amidase
  • Deficiency of amidinotransferase
  • Deficiency of amidophosphoribosyltransferase
  • Deficiency of amine oxidase
  • Deficiency of amine oxidase
  • Deficiency of aryl sulfotransferase
  • Deficiency of arylamine acetyltransferase
  • Deficiency of arylesterase
  • Deficiency of aspartic proteinase
  • Deficiency of azobenzene reductase
  • Deficiency of benzoylcholinesterase
  • Deficiency of butyrate-acetoacetate coenzyme A-transferase
  • Deficiency of carbamate kinase
  • Deficiency of carbon-carbon lyase
  • Deficiency of carbon-halide lyase
  • Deficiency of carbon-nitrogen lyase
  • Deficiency of carbon-oxygen lyase
  • Deficiency of carbon-sulfur lyase
  • Deficiency of carboxylesterase
  • Deficiency of carboxylic ester hydrolase
  • Deficiency of catechol oxidase
  • Deficiency of cathepsin C
  • Deficiency of cellulase
  • Deficiency of chlorophyllase
  • Deficiency of choline acetyltransferase
  • Deficiency of choline kinase
  • Deficiency of choline-phosphate cytidylyltransferase
  • Deficiency of cholinephosphotransferase
  • Deficiency of cholinesterase
  • Deficiency of chymosin
  • Deficiency of chymotrypsin
  • Deficiency of chymotrypsin A and B
  • Deficiency of citrate
  • Deficiency of creatine kinase
  • Deficiency of D-2-hydroxy-acid dehydrogenase
  • Deficiency of dehydrogenase
  • Deficiency of dehydrogluconate dehydrogenase
  • Deficiency of dehydrogluconokinase
  • Deficiency of deoxyribonuclease I
  • Deficiency of deoxyribonuclease II
  • Deficiency of deoxyribonucleic acid nucleotidylexotransferase
  • Deficiency of deoxyribonucleic acid-directed deoxyribonucleic acid polymerase
  • Deficiency of deoxyribonucleic acid-directed ribonucleic acid polymerase
  • Deficiency of dephospho-coenzyme A kinase
  • Deficiency of dextranase
  • Deficiency of dihydroorotase
  • Deficiency of diisopropyl-fluorophosphatase
  • Deficiency of dimethylallyltranstransferase
  • Deficiency of dioxygenase
  • Deficiency of dipeptidase
  • Deficiency of dipeptide hydrolase
  • Deficiency of dipeptidyl peptidase I
  • Deficiency of dipeptidyl-amino-peptidase I
  • Deficiency of dipeptidylpeptide hydrolase
  • Deficiency of diphosphomevalonate decarboxylase
  • Deficiency of diphosphoric monoester hydrolase
  • Deficiency of endopeptidase
  • Deficiency of endoribonuclease
  • Deficiency of enolase
  • Deficiency of enteropeptidase
  • Deficiency of epimerase
  • Deficiency of erythritol kinase
  • Deficiency of estradiol 6beta-monooxygenase
  • Deficiency of ethanolamine-phosphate cytidylyltransferase
  • Deficiency of ethanolaminephosphotransferase
  • Deficiency of ether hydrolase
  • Deficiency of exoribonuclease
  • Deficiency of formaldehyde dehydrogenase
  • Deficiency of formamidase
  • Deficiency of formate dehydrogenase
  • Deficiency of formate-tetrahydrofolate ligase
  • Deficiency of formiminotetrahydrofolate cyclodeaminase
  • Deficiency of formyltetrahydrofolate deformylase
  • Deficiency of fumarate hydratase
  • Deficiency of fumarylacetoacetase
  • Deficiency of galactonolactone dehydrogenase
  • Deficiency of glucosamine acetyltransferase
  • Deficiency of glucosamine kinase
  • Deficiency of glucosamine-phosphate acetyltransferase
  • Deficiency of glutathione reductase
  • Deficiency of glycerate kinase
  • Deficiency of glycerol-3-phosphate acyltransferase
  • Deficiency of glycerophosphatase
  • Deficiency of glycogen synthase a kinase
  • Deficiency of guanine deaminase
  • Deficiency of halogenase
  • Deficiency of heparin lyase
  • Deficiency of hexose oxidase
  • Deficiency of hexosyltransferase
  • Deficiency of histidinol dehydrogenase
  • Deficiency of hyaluronate lyase
  • Deficiency of hyaluronoglucosaminidase
  • Deficiency of hydrogen-sulfide acetyltransferase
  • Deficiency of hydrolase
  • Deficiency of hydrolyase
  • Deficiency of hydroxyacylglutathione hydrolase
  • Deficiency of hydroxyalkyl-protein kinase
  • Deficiency of hydroxymethylglutaryl-CoA hydrolase
  • Deficiency of hydroxymethylglutaryl-coenzyme A reductase
  • Deficiency of hydroxymethylglutaryl-coenzyme A synthase
  • Deficiency of imidodipeptidase
  • Deficiency of iminodipeptidase
  • Deficiency of inorganic pyrophosphatase
  • Deficiency of inosinase
  • Deficiency of inosine monophosphate cyclohydrolase
  • Deficiency of inosine monophosphate dehydrogenase
  • Deficiency of isobutyryl-coenzyme A dehydrogenase
  • Deficiency of isocitrate lyase
  • Deficiency of isomerase
  • Deficiency of isopentenyl-diphosphate delta-isomerase
  • Deficiency of ketotetrose-phosphate aldolase
  • Deficiency of lactonase
  • Deficiency of lactoylglutathione lyase
  • Deficiency of L-arabinose dehydrogenase
  • Deficiency of lecithinase D
  • Deficiency of leucine aminopeptidase
  • Deficiency of L-gulonate dehydrogenase
  • Deficiency of lichenase
  • Deficiency of ligase
  • Deficiency of limit dextrinase
  • Deficiency of lipophosphodiesterase II
  • Deficiency of L-prolylglycine dipeptidase
  • Deficiency of lyase
  • Deficiency of lysine-transfer ribonucleic acid ligase
  • Deficiency of lysolecithin acylmutase
  • Deficiency of lysophospholipase
  • Deficiency of lysozyme
  • Deficiency of malate dehydrogenase
  • Deficiency of malate dehydrogenase
  • Deficiency of malate dehydrogenase
  • Deficiency of malate oxidase
  • Deficiency of mannitol dehydrogenase
  • Deficiency of mannose-6-phosphate isomerase
  • Deficiency of metallocarboxypeptidase
  • Deficiency of metalloproteinase
  • Deficiency of methenyltetrahydrofolate cyclohydrolase
  • Deficiency of methylaspartate mutase
  • Deficiency of methylcrotonoyl-coenzyme A carboxylase
  • Deficiency of methylenetetrahydrofolate dehydrogenase
  • Deficiency of methylglutaconyl-coenzyme A hydratase
  • Deficiency of methylmalonyl-coenzyme A mutase
  • Deficiency of methyltransferase
  • Deficiency of mevaldate reductase
  • Deficiency of monodehydroascorbate reductase
  • Deficiency of monooxygenase
  • Deficiency of mutase
  • Deficiency of myo-inositol oxygenase
  • Deficiency of N-acetyl-beta-glucosaminidase
  • Deficiency of N-acetylneuraminate lyase
  • Deficiency of nicotinamide adenine dinucleotidase
  • Deficiency of nicotinamide adenine dinucleotide ^+^ kinase
  • Deficiency of nicotinamide adenine dinucleotide ^+^ nucleosidase
  • Deficiency of nicotinamide adenine dinucleotide ^+^ synthase
  • Deficiency of nicotinamide adenine dinucleotide phosphate ^+^ nucleosidase
  • Deficiency of nicotinamide adenine dinucleotide phosphate ^+^ transhydrogenase
  • Deficiency of nicotinamide methyltransferase
  • Deficiency of nicotinamide phosphoribosyltransferase
  • Deficiency of nicotinamide-nucleotide adenylyltransferase
  • Deficiency of nicotinate dehydrogenase
  • Deficiency of nicotinate phosphoribosyltransferase
  • Deficiency of nitrate reductase
  • Deficiency of non-specific cholinesterase
  • Deficiency of nucleosidase
  • Deficiency of nucleoside-diphosphatase
  • Deficiency of nucleoside-diphosphate kinase
  • Deficiency of nucleoside-phosphate kinase
  • Deficiency of nucleotidase
  • Deficiency of nucleotide pyrophosphatase
  • Deficiency of nucleotidyltransferase
  • Deficiency of omega peptidase
  • Deficiency of orotate phosphoribosyltransferase
  • Deficiency of oxalate coenzyme A-transferase
  • Deficiency of oxidase
  • Deficiency of oximinotransferase
  • Deficiency of oxo-acid-lyase
  • Deficiency of oxoglutarate dehydrogenase
  • Deficiency of oxygenase
  • Deficiency of pancreatic elastase
  • Deficiency of pantetheine kinase
  • Deficiency of pantetheine-phosphate adenylyltransferase
  • Deficiency of pantothenoylcysteine decarboxylase
  • Deficiency of pectin methoxylase
  • Deficiency of pectin methylesterase
  • Deficiency of pectinesterase
  • Deficiency of pentosyltransferase
  • Deficiency of pepsin A
  • Deficiency of pepsin B
  • Deficiency of peptidase a
  • Deficiency of peptide hydrolase
  • Deficiency of peptidoglycan endopeptidase
  • Deficiency of peroxidase
  • Deficiency of phenylalanine 4-monooxygenase
  • Deficiency of phenylpyruvate tautomerase
  • Deficiency of phosphatase
  • Deficiency of phosphatidate phosphatase
  • Deficiency of phosphoacetylglucosamine mutase
  • Deficiency of phosphoadenylate 3'-nucleotidase
  • Deficiency of phosphoamidase
  • Deficiency of phosphoglucomutase
  • Deficiency of phosphogluconate dehydrogenase
  • Deficiency of phosphogluconate dehydrogenase
  • Deficiency of phosphoglycerate mutase
  • Deficiency of phosphoketolase
  • Deficiency of phospholipase A>2<
  • Deficiency of phospholipase C
  • Deficiency of phospholipase D
  • Deficiency of phosphomevalonate kinase
  • Deficiency of phosphomonoesterase
  • Deficiency of phosphopantothenate-cysteine ligase
  • Deficiency of phosphoprotein phosphatase
  • Deficiency of phosphoribokinase
  • Deficiency of phosphoribosylamine-glycine ligase
  • Deficiency of phosphoribosylglycinamide formyltransferase
  • Deficiency of phosphoric diester hydrolase
  • Deficiency of phosphoric monoester hydrolase
  • Deficiency of phosphorus-oxygen lyase
  • Deficiency of phosphorylase kinase
  • Deficiency of phosphorylase phosphatase
  • Deficiency of phosphotransferase
  • Deficiency of plasmin
  • Deficiency of polygalacturonase
  • Deficiency of polyribonucleotide nucleotidyltransferase
  • Deficiency of progesterone 11alpha-monooxygenase
  • Deficiency of prolidase
  • Deficiency of prolinase
  • Deficiency of prolyl dipeptidase
  • Deficiency of protease
  • Deficiency of protein kinase
  • Deficiency of protocatechuate 3,4-dioxygenase
  • Deficiency of pyridoxal kinase
  • Deficiency of pyridoxamine-phosphate oxidase
  • Deficiency of pyrophosphotransferase
  • Deficiency of pyrroline-2-carboxylate reductase
  • Deficiency of pyruvate kinase
  • Deficiency of racemase
  • Deficiency of reduced nicotinamide adenine dinucleotide dehydrogenase
  • Deficiency of reduced nicotinamide adenine dinucleotide phosphate dehydrogenase
  • Deficiency of reductase
  • Deficiency of renin
  • Deficiency of retinal isomerase
  • Deficiency of retinyl-palmitate esterase
  • Deficiency of riboflavin kinase
  • Deficiency of riboflavin mononucleotide adenylyltransferase
  • Deficiency of ribokinase
  • Deficiency of ribonuclease
  • Deficiency of ribose-5-phosphate isomerase
  • Deficiency of ribose-phosphate pyrophosphokinase
  • Deficiency of ribosomal cathepsin
  • Deficiency of ribosomal neutral proteinase
  • Deficiency of ribosylnicotinamide kinase
  • Deficiency of ribulokinase
  • Deficiency of ribulose-phosphate 3-epimerase
  • Deficiency of sedoheptulokinase
  • Deficiency of serine proteinase
  • Deficiency of shikimate dehydrogenase
  • Deficiency of sialidase
  • Deficiency of squalene monooxygenase
  • Deficiency of steroid 17-alpha-monooxygenase
  • Deficiency of steroid delta-isomerase
  • Deficiency of succinate- coenzyme A ligase
  • Deficiency of succinate dehydrogenase
  • Deficiency of succinate-coenzyme A ligase
  • Deficiency of succinate-coenzyme A ligase
  • Deficiency of succinyl-coenzyme A hydrolase
  • Deficiency of sulfatase
  • Deficiency of sulfate adenylyltransferase
  • Deficiency of sulfinoalanine decarboxylase
  • Deficiency of sulfite reductase
  • Deficiency of sulfotransferase
  • Deficiency of sulfuric ester hydrolase
  • Deficiency of sulfurtransferase
  • Deficiency of tannase
  • Deficiency of thiamin pyridinylase
  • Deficiency of thiamin pyrophosphokinase
  • Deficiency of thioethanolamine acetyltransferase
  • Deficiency of thioether hydrolase
  • Deficiency of thiolester hydrolase
  • Deficiency of thiosulfate sulfurtransferase
  • Deficiency of thrombin
  • Deficiency of transacylase
  • Deficiency of transaldolase
  • Deficiency of transcarbamoylase
  • Deficiency of transcarboxylase
  • Deficiency of transferase
  • Deficiency of transformiminase
  • Deficiency of transformylase
  • Deficiency of transhydroxymethylase
  • Deficiency of transketolase
  • Deficiency of triacylglycerol lipase
  • Deficiency of tripeptide aminopeptidase
  • Deficiency of triphosphoric monoester hydrolase
  • Deficiency of tropinesterase
  • Deficiency of true cholinesterase
  • Deficiency of trypsin
  • Deficiency of tyraminase
  • Deficiency of tyrosine aminotransferase
  • Deficiency of unspecific monooxygenase
  • Deficiency of uracil dehydrogenase
  • Deficiency of uracil phosphoribosyltransferase
  • Deficiency of urate oxidase
  • Deficiency of uridine diphosphate-glucose dehydrogenase
  • Deficiency of uridine triphosphate-glucose-1-phosphate uridylyltransferase
  • Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase
  • Deficiency of uronolactonase
  • Deficiency of w-amidase
  • Deficiency of xylan endo-1,3-beta-xylosidase
  • Dilated cardiomyopathy secondary to deficiency
  • Dilated cardiomyopathy secondary to electrolyte deficiency
  • Dilated cardiomyopathy secondary to familial storage disease
  • Dilated cardiomyopathy secondary to metabolic disorder
  • Dilated cardiomyopathy secondary to metabolic disorder
  • Disorder due cytochrome p450 CYP2C19 variant
  • Disorder due cytochrome p450 CYP2C9 variant
  • Disorder due cytochrome p450 CYP2D6 variant
  • Disorder due to cytochrome p450 enzyme variant
  • Disorder due to N-acetyltransferase enzyme variant
  • Disorder of blood gas
  • Disorder of cortisol-cortisone shuttle
  • Disorder of iodine metabolism
  • Disorder of lipid metabolism
  • Disorder of lysosomal enzyme
  • Disorder of organic acid metabolism
  • Disorder of oxygen transport
  • Disorder of propionate AND/OR methylmalonate metabolism
  • Disorder of protein metabolism
  • Disorder of sialic acid metabolism
  • Disorder of sialic acid metabolism
  • Disorder of steroid metabolism
  • Enterokinase deficiency
  • Erythrocyte enzyme deficiency
  • Ethanolaminosis
  • Etiocholanolone fever
  • Extensive metabolizer due to cytochrome p450 CYP2D6 variant
  • Familial cardiomyopathy
  • Fast acetylator due to N-acetyltransferase enzyme variant
  • Folic acid deficiency
  • Folic acid deficiency
  • Fumarase deficiency
  • Fumarylacetoacetase deficiency, acute type
  • Genetic polymorphism
  • Glucose phosphate isomerase deficiency
  • Glutathione S-transferase deficiency
  • Gronblad-Strandberg syndrome
  • Hyperimidodipeptiduria due to proline dipeptidase deficiency
  • Hyperthermia-hyperphagia-hypothyroidism syndrome
  • Impaired oxygen delivery
  • Impaired oxygen extraction
  • Increased oxygen demand
  • Inflammation of bursa of patella
  • Inherited disorder of folate metabolism
  • Intermediate metabolizer due to cytochrome p450 CYP2D6 variant
  • Intestinal enteropeptidase deficiency
  • Ketonemia
  • Ketosis
  • Ketotic hypoglycemia
  • Liposynovitis prepatellaris
  • Madelung's neck
  • Metabolic disorder of transport
  • Methylcrotonic aciduria
  • Mitochondrial 2-methylacetoacetyl-coenzyme A thiolase deficiency - non-potassium stimulated
  • Mucolipidosis
  • Muscle D-lactate dehydrogenase deficiency
  • Non-amino organic acidemia AND/OR aciduria
  • Pancreatic colipase deficiency
  • Pancreatic malabsorption
  • Partial deficiency of methylmalonyl-coenzyme A mutase
  • Phosphoglycerokinase 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
  • Prepatellar bursitis
  • Proteinosis
  • Pseudohypoaldosteronism
  • Pseudohypoaldosteronism type 2A
  • Pseudohypoaldosteronism, type 1
  • Pseudohypoaldosteronism, type 1, dominant form
  • Pseudohypoaldosteronism, type 1, recessive form
  • Pseudohypoaldosteronism, type 2
  • Pyridoxine dependency syndrome
  • Rowley-Rosenberg syndrome
  • Sialic acid storage disease, severe infantile type
  • Sialic storage disease
  • Sialuria
  • Slow acetylator due to N-acetyltransferase enzyme variant
  • Specific enzyme deficiency
  • Testosterone 17-beta-dehydrogenase deficiency
  • Trypsinogen deficiency
  • UGT1A1*28 polymorphism
  • Ultrarapid metabolizer due to cytochrome p450 CYP2D6 variant

Index of Diseases and Injuries
References found for the code E88.89 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. There are different groups of disorders. Some affect the breakdown of amino acids, carbohydrates, or lipids. Another group, mitochondrial diseases, affects the parts of the cells that produce the energy.

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.

  • Acidosis (Medical Encyclopedia)
  • Alkalosis (Medical Encyclopedia)
  • Lactic acid test (Medical Encyclopedia)
  • Metabolic acidosis (Medical Encyclopedia)
  • Metabolic neuropathies (Medical Encyclopedia)
  • Pseudohypoparathyroidism (Medical Encyclopedia)


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