2007 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 2007 version of ICD-9-CM 271.8.
- More recent version(s) of ICD-9-CM 271.8: 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
alpha-fucosidase 271.8
fucosidase 271.8
