Specific code 2006 ICD-9-CM Diagnosis Code 271.8
Other specified disorders of carbohydrate transport and metabolism
  • Short description: DIS CARBOHYDR METAB NEC.
  • ICD-9-CM 271.8 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 271.8 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 2006 version of ICD-9-CM 271.8.
  • More recent version(s) of ICD-9-CM 271.8: 2007 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: 271.8 converts approximately to:
  • 2015/16 ICD-10-CM E72.52 Trimethylaminuria
    Or:
  • 2015/16 ICD-10-CM E72.53 Hyperoxaluria
    Or:
  • 2015/16 ICD-10-CM E74.4 Disorders of pyruvate metabolism and gluconeogenesis
    Or:
  • 2015/16 ICD-10-CM E74.8 Other specified disorders of carbohydrate metabolism
    Or:
  • 2015/16 ICD-10-CM E77.1 Defects in glycoprotein degradation
Approximate Synonyms
  • Acquired monosaccharide malabsorption
  • Adult fucosidosis
  • alpha, alpha-Trehalase deficiency
  • Antifreeze oxalosis
  • Beta-D-mannosidosis
  • Carbohydrate deficiency glycoprotein syndrome
  • Carbohydrate deficient glycoprotein syndrome
  • Carbohydrate-deficient glycoprotein syndrome
  • Carbohydrate-deficient glycoprotein syndrome type II
  • Carbohydrate-deficient glycoprotein syndrome type III
  • Deficiency of alpha-mannosidase
  • Deficiency, pyruvate carboxylase
  • Deficiency, pyruvate deshydrogenase
  • Disorder of carbohydrate absorption
  • Disorder of glucose metabolism
  • Disorder of glycerate metabolism
  • Disorder of glycoprotein metabolism
  • Disorders of pyruvate metabolism and gluconeogenesis
  • Dysglycemia
  • Enteric hyperoxaluria
  • Essential benign pentosuria
  • Essential pentosuria
  • Fucosidosis
  • Glycoprotein metabolism disorder
  • Hyperglycemic disorder
  • Hyperoxaluria
  • Impaired glucose tolerance associated with genetic syndrome
  • Impaired intestinal epithelial cell transport of carbohydrates
  • Infantile fucosidosis
  • Insulin resistance - type A
  • Insulin resistance - type B
  • Juvenile fucosidosis
  • Lactate dehydrogenase deficiency
  • Mannosidosis
  • Mannosidosis, type I
  • Mannosidosis, type II
  • Nonglucosuric melituria
  • Oxalosis
  • Primary hyperoxaluria
  • Primary hyperoxaluria, type I
  • Primary hyperoxaluria, type II
  • Pyruvate carboxylase deficiency
  • Pyruvate dehydrogenase complex deficiency
  • Pyruvate dehydrogenase deficiency
  • Pyruvate metabolism and gluconeogenesis disorder
  • Secondary oxalosis
  • Sialidosis
  • Syndrome of carbohydrate intolerance
  • Xylosuria
Applies To
  • Essential benign pentosuria
  • Fucosidosis
  • Glycolic aciduria
  • Hyperoxaluria (primary)
  • Mannosidosis
  • Oxalosis
  • Xylosuria
  • Xylulosuria
ICD-9-CM Volume 2 Index entries containing back-references to 271.8:
  • Absence (organ or part) (complete or partial)
    • alpha-fucosidase 271.8
    • fucosidase 271.8
  • Aciduria 791.9
    • glycolic 271.8
  • Bird's disease (oxaluria) 271.8
  • Carbohydrate-deficient glycoprotein syndrome (CDGS) 271.8
  • CDGS (carbohydrate-deficient glycoprotein syndrome) 271.8
  • Deficiency, deficient
    • alpha-fucosidase 271.8
    • alpha-mannosidase 271.8
    • fucosidase 271.8
    • mannosidase 271.8
    • phosphoenolpyruvate carboxykinase 271.8
    • phosphomannomutase 271.8
    • phosphomannose isomerase 271.8
    • phosphomannosyl mutase 271.8
    • pyruvate carboxylase 271.8
    • pyruvate dehydrogenase 271.8
  • Diathesis
    • oxalic 271.8
  • Disease, diseased - see also Syndrome
    • Bird's (oxaluria) 271.8
  • Disorder - see also Disease
    • congenital
      • glycosylation (CDG) 271.8
    • infant sialic acid storage 271.8
    • transport, carbohydrate 271.9
      • specified type NEC 271.8
  • Fucosidosis 271.8
  • Hyperoxaluria (primary) 271.8
  • L-xyloketosuria 271.8
  • Malabsorption 579.9
    • monosaccharide 271.8
  • Mannoheptulosuria 271.8
  • Mannosidosis 271.8
  • Oxalosis 271.8
  • Oxaluria 271.8
  • Pentosuria (benign) (essential) 271.8
  • Syndrome - see also Disease
    • carbohydrate-deficient glycoprotein (CDGS) 271.8
  • Xyloketosuria 271.8
  • Xylosuria 271.8
  • Xylulosuria 271.8
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 271.8 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2006 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.