Diagnosis Code: E72.89

Short Description: Other specified disorders of amino-acid metabolism

Long Description: Other specified disorders of amino-acid metabolism

The code E72.89 is VALID for claim submission

Code Classification:

• Endocrine, nutritional and metabolic diseases (E00–E89)
  • Metabolic disorders (E70-E88)
    • Other disorders of amino-acid metabolism (E72)
      • E72.89 Other specified disorders of amino-acid metabolism

Code Version: 2022 ICD-10-CM

Synonyms

• 2-hydroxyglutaric aciduria
• 3-Phosphoglycerate dehydrogenase deficiency
• 3-phosphoglycerate dehydrogenase deficiency infantile form
• 3-phosphoglycerate dehydrogenase deficiency juvenile form
• 5-Oxoprolinase deficiency
• Alaninemia
• Alpha ketoadipic aciduria
• Aminoacidemia
• Aminoaciduria
• Aminoaciduria
• Aminoaciduria
• Camptodactyly of finger
• Camptodactyly taurinuria syndrome
• Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
• Congenital porphyria
• Deficiency of 3-hydroxyisobutyrate dehydrogenase
• Deficiency of 4-hydroxy-2-oxoglutarate aldolase
• Deficiency of A-ase
• Deficiency of acid-aminoacid ligase
• Deficiency of adenosylhomocysteinase
• Deficiency of alanine aminotransferase
• Deficiency of alanine dehydrogenase
• Deficiency of alanine-oxo-acid aminotransferase
• Deficiency of alanine-tRNA ligase
• Deficiency of aminoacylase 1
• Deficiency of aminoacyl-histidine dipeptidase
• Deficiency of aminoacyltransferase
• Deficiency of aminopeptidase
• Deficiency of aminotransferase
• Deficiency of ammonia-lyase
• Deficiency of asparagine-oxo-acid aminotransferase
• Deficiency of aspartate 4-decarboxylase
• Deficiency of aspartate aminotransferase
• Deficiency of aspartate kinase
• Deficiency of betaine-aldehyde dehydrogenase
• Deficiency of betaine-homocysteine methyltransferase
• Deficiency of carboxy-lyase
• Deficiency of carboxypeptidase A
• Deficiency of carboxypeptidase B
• Deficiency of carnosinase
• Deficiency of choline dehydrogenase
• Deficiency of cysteamine dioxygenase
• Deficiency of cysteine aminotransferase
• Deficiency of cysteine carboxypeptidase
• Deficiency of cysteine proteinase
• Deficiency of cysteinyl-glycine dipeptidase
• Deficiency of cystine reductase
• Deficiency of cytosol aminopeptidase
• Deficiency of D-amino-acid oxidase
• Deficiency of D-aspartate oxidase
• Deficiency of glutamate decarboxylase
• Deficiency of glutamate dehydrogenase
• Deficiency of glutamate-ammonia ligase
• Deficiency of glutaminase
• Deficiency of glutamine phenylacetyltransferase
• Deficiency of glutamine-fructose-6-phosphate aminotransferase
• Deficiency of glutamine-pyruvate aminotransferase
• Deficiency of glycine amidinotransferase
• Deficiency of glycine hydroxymethyltransferase
• Deficiency of guanidinoacetate kinase
• Deficiency of guanidinoacetate methyltransferase
• Deficiency of homoserine kinase
• Deficiency of L-amino-acid oxidase
• Deficiency of L-asparagine amidohydrolase
• Deficiency of L-serine ammonia-lyase
• Deficiency of malonate CoA-transferase
• Deficiency of N-methyl-L-amino-acid oxidase
• Deficiency of phosphoserine phosphatase
• Deficiency of proline dipeptidase
• Deficiency of pyrroline-5-carboxylate reductase
• Deficiency of serine carboxypeptidase
• Deficiency of serine-tRNA ligase
• Deficiency of threonine aldolase
• Deficiency of threonine dehydratase
• Deficiency of threonine-tRNA ligase
• Dibasic aminoaciduria
• Dicarboxylic aminoaciduria syndrome
• Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism
• Disorder of beta and omega amino acid metabolism
• Disorder of creatine synthesis
• Disorder of glutamine metabolism
• Disorder of glutamine metabolism
• Disorder of glutamine metabolism
• Disorder of phenylalanine metabolism
• Disorder of proline AND/OR hydroxyproline metabolism
• Disorder of serine metabolism
• Disorder of tetrahydrobiopterin metabolism
• Disorder of the gamma-glutamyl cycle
• Disorder of threonine metabolism
• Erythropoietic protoporphyria
• Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
• Ferrochelatase deficiency
• Gamma-glutamyl transpeptidase deficiency
• Glutamate-cysteine ligase deficiency
• Glutathione synthase deficiency with 5-oxoprolinuria
• Glutathione synthase deficiency without 5-oxoprolinuria
• Glutathione synthetase deficiency
• Glutathionemia
• Glycoprolinuria
• Hereditary camptodactyly
• Homocarnosinase deficiency
• Hyper-beta-alaninemia
• Hyper-beta-carnosinemia
• Hyperdicarboxylicaminoaciduria AND hyperprolinemia
• Hyperhydroxyprolinemia
• Hyperprolinemia
• Iminoacidopathy
• Inborn error of glutathione metabolism
• Inherited aminoaciduria
• Inherited aminoaciduria
• Inherited aminoaciduria
• Lysinuric protein intolerance
• Neonatal epileptic encephalopathy due to glutaminase deficiency
• Phosphoserine aminotransferase deficiency
• Pipecolic acidemia
• Prolinuria
• Spastic ataxia, dysarthria due to glutaminase deficiency
• Succinate-semialdehyde dehydrogenase deficiency

References to Index of Diseases and Injuries

The code E72.89 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Disorders of beta-amino-acid metabolism
  • Disorders of gamma-glutamyl cycle

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This page was last updated on: 10/1/2023

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