270.8 DIS AMINO-ACID METAB NEC

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		E72.03	Lowe's syndrome
		E72.8	Other specified disorders of amino-acid metabolism

Similar Codes