2015 ICD-9-CM Diagnosis Code 270.8
Other specified disorders of amino-acid metabolism
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 270.8 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 270.8 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).
Convert to ICD-10-CM:
270.8 converts approximately to:
- 2015/16 ICD-10-CM E72.03 Lowe's syndrome
Or:
- 2015/16 ICD-10-CM E72.8 Other specified disorders of amino-acid metabolism
Approximate Synonyms
- 2-Ketoadipic acidemia
- 5-Oxoprolinase deficiency
- Abnormal amino acid sequence
- Acidemia, isovaleric
- Aciduria, ketoadipic
- Alaninemia
- Alpha ketoadipic aciduria
- Aminomethyltransferase deficiency
- Aromatic amino acid decarboxylase deficiency
- Beta-hydroxyisobutyryl-CoA deacylase deficiency
- Biotin- ligase deficiency
- Carnosinuria
- Cobalamin D disease
- D-2 glutaric aciduria
- Disorder of amino acid and organic acid metabolism
- Disorder of aromatic amino acid metabolism
- Disorder of beta and omega amino acid metabolism
- Disorder of catecholamine synthesis
- Disorder of creatine synthesis
- Disorder of isoleucine metabolism
- Disorder of lysine and hydroxylysine metabolism
- Disorder of phenylalanine metabolism
- Disorder of proline AND/OR hydroxyproline metabolism
- Disorder of propionate AND/OR methylmalonate metabolism
- Disorder of tetrahydrobiopterin metabolism
- Disorder of the gamma-glutamyl cycle
- Disorder of valine metabolism
- Dopamine beta-hydroxylase deficiency
- Ethanolaminosis
- Familial renal iminoglycinuria
- gamma-Glutamyltransferase deficiency
- Glucoaminophosphaturia syndrome
- Glucoaminophosphaturia syndrome with rickets
- Glutamate formiminotransferase deficiency
- Glutamate-cysteine ligase deficiency
- Glutaric aciduria
- Glutathione synthase deficiency with 5-oxoprolinuria
- Glutathionemia
- Glycoprolinuria
- Hyper-beta-alaninemia
- Hyperdicarboxylicaminoaciduria AND hyperprolinemia
- Hyperhydroxyprolinemia
- Hyperprolinemia
- Iminoacidopathy
- Iminoglycinuria
- Inborn error of glutathione metabolism
- Isovaleric acidemia
- Isovaleryl-CoA dehydrogenase deficiency
- Lowe syndrome
- Lysinuric protein intolerance
- Ornithine oxo-acid aminotransferase deficiency
- Proline dehydrogenase deficiency
- Prolinuria
- Propionyl-CoA carboxylase deficiency pccA complementation group
- Propionyl-CoA carboxylase deficiency pccBC complementation group
- Sarcosine dehydrogenase deficiency
- Succinyl-CoA acetoacetate transferase deficiency
- Trimethylaminuria
Applies To
- Alaninemia
- Ethanolaminuria
- Glycoprolinuria
- Hydroxyprolinemia
- Hyperprolinemia
- Iminoacidopathy
- Prolinemia
- Prolinuria
- Sarcosinemia