270.8 DIS AMINO-ACID METAB NEC


Code Information

Diagnosis Code: 270.8

Short Description: Dis amino-acid metab NEC

Long Description: Other specified disorders of amino-acid metabolism

Code Classification:

  • Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279)
    • Other metabolic disorders and immunity disorders (270-279)
      • 270 Disorders of amino-acid transport and metabolism
        • 270.8 Dis amino-acid metab NEC

Code Version: 2015 ICD-9-CM


Synonyms

  • 2-hydroxyglutaric aciduria
  • 5-Oxoprolinase deficiency
  • Abnormal amino acid sequence
  • Alaninemia
  • Aminomethyltransferase deficiency
  • Aromatic amino acid decarboxylase deficiency
  • Beta-hydroxyisobutyryl-coenzyme A deacylase deficiency
  • Biotin-
  • Carnosinuria
  • Cerebral creatine deficiency syndrome 3
  • Cobalamin D disease
  • D-2-hydroxyglutaric 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
  • Lowe syndrome
  • Lysinuric protein intolerance
  • Ornithine oxo-acid aminotransferase deficiency
  • Proline dehydrogenase deficiency
  • Prolinuria
  • Propionyl-coenzyme A carboxylase deficiency pccA complementation group
  • Propionyl-coenzyme A carboxylase deficiency pccBC complementation group
  • Sarcosine dehydrogenase deficiency
  • Succinyl-coenzyme A acetoacetate transferase deficiency

References to Index of Diseases and Injuries

The code 270.8 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Alaninemia 270.8
  • Disorder - see also Disease
    • amino acid (metabolic) (see also Disturbance, metabolism, amino acid) 270.9
      • specified type NEC 270.8
    • metabolism NEC 277.9
      • amino acid (see also Disorder, amino acid) 270.9
        • specified type NEC 270.8
  • Disturbance - see also Disease
    • metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9
      • amino acid (see also Disorder, amino acid) 270.9
        • specified type NEC 270.8
  • Dystrophy, dystrophia 783.9
    • oculocerebrorenal 270.8
  • Ethanolaminuria 270.8
  • Glycoprolinuria 270.8
  • Hydroxyprolinemia 270.8
  • Hydroxyprolinuria 270.8
  • Hyperprolinemia 270.8
  • Hypersarcosinemia 270.8
  • Iminoacidopathy 270.8
  • Iminoglycinuria, familial 270.8
  • Lowe (-Terrey-MacLachlan) syndrome (oculocerebrorenal dystrophy) 270.8
  • Prolinemia 270.8
  • Prolinuria 270.8
  • Sarcosinemia 270.8
  • Syndrome - see also Disease
    • fish odor 270.8
    • Lowe's (oculocerebrorenal dystrophy) 270.8
    • Lowe-Terrey-MacLachlan (oculocerebrorenal dystrophy) 270.8
  • Trimethylaminuria 270.8

Crosswalk Information

The code 270.8 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
270.8 Right Arrow E72.03 Lowe's syndrome
E72.8 Other specified disorders of amino-acid metabolism
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
270.0 Disturbances of amino-acid transport
270.1 Phenylketonuria [PKU]
270.2 Other disturbances of aromatic amino-acid metabolism
270.3 Disturbances of branched-chain amino-acid metabolism
270.4 Disturbances of sulphur-bearing amino-acid metabolism
270.5 Disturbances of histidine metabolism
270.6 Disorders of urea cycle metabolism
270.7 Other disturbances of straight-chain amino-acid metabolism
270.9 Unspecified disorder of amino-acid metabolism


This page was last updated on: 10/1/2014