E72.89
BillableOther specified disorders of amino-acid metabolism
Other specified disorders of amino-acid metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Disorders of beta-amino-acid metabolism
- Disorders of gamma-glutamyl cycle
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout (M1A.-, M10.-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hyper-beta-alaninaemia2359002
- Hyper-beta-alaninemia2359002
- Hyperalaninaemia2359002
- Hyperalaninemia2359002
- Disorder of gamma-glutamyl cycle9128006
- Disorder of the gamma-glutamyl cycle9128006
- Disorder of phenylalanine metabolism12957008
- Pipecolic acidaemia13306007
- Pipecolic acidemia13306007
- Hydroxyprolinaemia25739007
- Hydroxyprolinemia25739007
- Hyperhydroxyprolinaemia25739007
- Hyperhydroxyprolinemia25739007
- 5-Oxoprolinase deficiency26132002
- Pyroglutamate hydrolase deficiency26132002
- Deficiency of glutamate-cysteine ligase36799008
- Gamma-glutamyl cysteine synthase deficiency36799008
- Gamma-glutamylcysteine synthetase deficiency36799008
- Glutamate-cysteine ligase deficiency36799008
- Disorder of proline AND/OR hydroxyproline metabolism37800003
- Disorder of proline and hydroxyproline metabolism37800003
- Hyperdicarboxylicaminoaciduria AND hyperprolinaemia37982009
- Hyperdicarboxylicaminoaciduria AND hyperprolinemia37982009
- 5-Oxoprolinuria39112005
- Glutathione synthase deficiency with 5-oxoprolinuria39112005
- Glycoprolinuria45188008
- Aminoacidaemia46556004
- Aminoacidemia46556004
- Glutathionaemia47906008
- Glutathionemia47906008
- 4-Hydroxybutyric aciduria49748000
- GABA metabolic defect49748000
- GABAuria49748000
- Gamma-hydroxybutyric acidaemia49748000
- Gamma-hydroxybutyric acidemia49748000
- SSADH (succinic semialdehyde dehydrogenase) deficiency49748000
- Succinate-semialdehyde dehydrogenase deficiency49748000
- Succinic semialdehyde dehydrogenase deficiency49748000
- gamma-Hydroxybutyric aciduria49748000
- EPP - erythropoietic protoporphyria51022005
- Erythrohepatic protoporphyria51022005
- Erythropoietic protoporphyria51022005
- Haem synthase deficiency51022005
- Heme synthase deficiency51022005
- Magnus syndrome51022005
- Protoporphyria51022005
- Prolinuria53124003
- Hyperprolinaemia59655002
- Hyperprolinemia59655002
- Homocarnosinase deficiency61764000
- Homocarnosinosis61764000
- Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism61961002
- Inborn error of glutathione metabolism72262000
- Gamma-glutamyl transferase deficiency78586005
- Gamma-glutamyl transpeptidase deficiency78586005
- Glutathionuria78586005
- Deficiency of 3-hydroxyisobutyrate dehydrogenase124119008
- HIBADH-gene related deficiency of 3-hydroxyisobutyrate dehydrogenase124119008
- Deficiency of choline dehydrogenase124148002
- Deficiency of betaine-aldehyde dehydrogenase124157008
- Deficiency of alanine dehydrogenase124168008
- Deficiency of glutamate dehydrogenase124169000
- Deficiency of glutamic dehydrogenase124169000
- Deficiency of D-aspartate oxidase124170004
- Deficiency of L-amino-acid oxidase124171000
- Deficiency of ophio-amino acid oxidase124171000
- Deficiency of D-amino-acid oxidase124172007
- Deficiency of pyrroline-5-carboxylate reductase124177001
- Pyrroline-5-carboxylate reductase deficiency124177001
- delta'-Pyrroline-5-carboxylate dehydrogenase deficiency124177001
- Deficiency of N-methyl-L-amino-acid oxidase124182008
- Deficiency of cystine reductase (NADH)124187002
- Deficiency of cystine reductase (reduced nicotinamide adenine dinucleotide)124187002
- Deficiency of cysteamine dioxygenase124209008
- Deficiency of guanidinoacetate methyltransferase124239003
- Guanidinoacetate methyltransferase deficiency124239003
- Deficiency of betaine-homocysteine methyltransferase124242009
- Deficiency of glycine hydroxymethyltransferase124243004
- Deficiency of serine aldolase124243004
- Deficiency of serine hydroxymethylase124243004
- Deficiency of glycine amidinotransferase124250000
- Deficiency of glutamine phenylacetyltransferase124263006
- Deficiency of GOT (glutamate oxaloacetate transaminase)124284001
- Deficiency of SGOT (serum glutamic-oxaloacetic transaminase)124284001
- Deficiency of aspartate aminotransferase124284001
- Deficiency of glutamic-aspartic transaminase124284001
- Deficiency of glutamic-oxaloacetic transaminase124284001
- Deficiency of GPT (glutamic pyruvic transaminase)124285000
- Deficiency of SGPT (serum glutamic pyruvic transaminase)124285000
- Deficiency of alanine aminotransferase124285000
- Deficiency of glutamic-alanine transaminase124285000
- Deficiency of cysteine aminotransferase124286004
- Deficiency of alanine-oxo-acid aminotransferase124291003
- Deficiency of asparagine-oxo-acid aminotransferase124293000
- Deficiency of glutaminase II124294006
- Deficiency of glutamine transaminase L124294006
- Deficiency of glutamine-oxo-acid transaminase124294006
- Deficiency of glutamine-pyruvate aminotransferase124294006
- Deficiency of glucosamine-6-phosphate isomerase (glutamine-forming)124295007
- Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerising)124295007
- Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerizing)124295007
- Deficiency of hexosephosphate aminotransferase124295007
- Deficiency of homoserine kinase124330001
- Deficiency of aspartate kinase124336007
- Deficiency of aspartokinase124336007
- Deficiency of guanidinoacetate kinase124337003
- Deficiency of malonate CoA-transferase124365001
- Deficiency of aminoacyltransferase124384003
- Deficiency of aminotransferase124394008
- Deficiency of transaminase124394008
- Deficiency of hydrolase124407008
- Deficiency of choline phosphatase124432005
- Deficiency of phosphoserine phosphatase124432005
- Deficiency of adenosylhomocysteinase124481007
- Deficiency of cysteinyl-glycine dipeptidase124486002
- Deficiency of serine carboxypeptidase124491001
- Deficiency of carboxypeptidase A124492008
- Deficiency of carboxypolypeptidase124492008
- Deficiency of carboxypeptidase B124493003
- Deficiency of protaminase124493003
- Deficiency of glutaminase124507006
- Deficiency of cysteine carboxypeptidase124581005
- Deficiency of cysteine proteinase124587009
- Deficiency of aspartate 4-decarboxylase124595008
- Deficiency of desulfinase124595008
- Deficiency of desulphinase124595008
- Deficiency of glutamate decarboxylase124596009
- Deficiency of threonine aldolase124606005
- Deficiency of 2-oxo-4-hydroxyglutarate aldolase124614004
- Deficiency of 4-hydroxy-2-oxoglutarate aldolase124614004
- Deficiency of L-hydroxyaminoacid dehydratase124619009
- Deficiency of L-serine ammonia-lyase124619009
- Deficiency of L-serine deaminase124619009
- Deficiency of L-serine dehydratase124619009
- Deficiency of serine deaminase124619009
- Deficiency of threonine deaminase124620003
- Deficiency of threonine dehydratase124620003
- Deficiency of carboxy-lyase124638000
- Deficiency of decarboxylase124638000
- Deficiency of ammonia-lyase124650006
- Deficiency of threonine-tRNA ligase124690009
- Deficiency of threonine-transfer ribonucleic acid ligase124690009
- Deficiency of threonyl-tRNA synthetase124690009
- Deficiency of alanine-tRNA ligase124694000
- Deficiency of alanine-transfer ribonucleic acid ligase124694000
- Deficiency of alanyl-tRNA synthetase124694000
- Deficiency of serine-tRNA ligase124697007
- Deficiency of serine-transfer ribonucleic acid ligase124697007
- Deficiency of seryl-tRNA synthetase124697007
- Deficiency of glutamate-ammonia ligase124704002
- Deficiency of glutamine synthetase124704002
- Deficiency of acid-aminoacid ligase124723009
- Deficiency of peptide synthase124723009
- Disorder of threonine metabolism190722000
- Disturbance of threonine metabolism190722000
- Disorder of glutamine metabolism190724004
- Disturbance of glutamine metabolism190724004
- Alaninaemia190732007
- Alaninemia190732007
- Iminoacidopathy190737001
- Congenital porphyria190913009
- Glutathione synthetase deficiency234589002
- Pyroglutamic aciduria234589002
- Pyroglutamicaciduria234589002
- Dibasic aminoaciduria236475007
- Disorder of tetrahydrobiopterin metabolism237913008
- Erythrocyte glutathione synthase deficiency237926007
- Glutathione synthase deficiency without 5-oxoprolinuria237926007
- Disorder of beta and omega amino acid metabolism237940008
- Hereditary camptodactyly238855000
- Hyper-beta-carnosinaemia273700000
- Hyper-beta-carnosinemia273700000
- FECH - Ferrochelatase deficiency276265003
- Ferrochelatase deficiency276265003
- Disorder of creatine synthesis297226004
- Disorder of serine metabolism303097007
- 3-Phosphoglycerate dehydrogenase deficiency303098002
- Congenital lysinuria303852004
- Hyperdibasic aminoaciduria303852004
- LPI - Lysinuric protein intolerance303852004
- Lysinuric protein intolerance303852004
- Deficiency of aminopeptidase360932008
- Deficiency of carnosinase360943000
- Deficiency of aminoacyl-histidine dipeptidase360953004
- Deficiency of L-asparaginase361087002
- Deficiency of L-asparagine amidohydrolase361087002
- Deficiency of asparaginase361087002
- Alpha ketoadipic aciduria443894002
- 2-hydroxyglutaric aciduria698870008
- Inherited aminoaciduria698953004
- Aminoacylase 1 deficiency709282004
- Deficiency of aminoacylase 1709282004
- Combined D-2-hydroxyglutaric acidaemia and L-2-hydroxyglutaric acidaemia713401006
- Combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia713401006
- Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria713401006
- D,L-2-hydroxyglutaric acidaemia713401006
- D,L-2-hydroxyglutaric acidemia713401006
- Dicarboxylic aminoaciduria syndrome716747007
- Glutamate aspartate transport defect716747007
- Deficiency of phosphoserine aminotransferase718603002
- Phosphoserine aminotransferase deficiency718603002
- Camptodactyly taurinuria syndrome733466005
- Familial streblodactyly with amino-aciduria733466005
- 3-phosphoglycerate dehydrogenase deficiency juvenile form733636005
- 3-phosphoglycerate dehydrogenase deficiency infantile form733637001
- Camptodactyly of finger1162716000
- Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 21186810009
- Neonatal epileptic encephalopathy due to deficiency of glutaminase1222662000
- Neonatal epileptic encephalopathy due to glutaminase deficiency1222662000
- Spastic ataxia, dysarthria due to glutaminase deficiency1255323007
- Serine biosynthesis pathway deficiency, infantile/juvenile form1284855000
- Disorder of GABA (gamma aminobutyric acid) metabolism16909721000119103
- Disorder of gamma aminobutyric acid metabolism16909721000119103
- Disorder of gamma-aminobutyric acid metabolism16909721000119103
Frequently Asked Questions
What is the ICD-10 code for other specified disorders of amino-acid metabolism?
The ICD-10-CM code for other specified disorders of amino-acid metabolism is E72.89. The full clinical description is "Other specified disorders of amino-acid metabolism". E72.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.89 mean?
ICD-10-CM code E72.89 represents "Other specified disorders of amino-acid metabolism". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E72.89 a billable code?
Yes, E72.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.89 in?
E72.89 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.89?
E72.89 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 9 more.
What SNOMED CT codes does E72.89 map to?
E72.89 maps to 111 SNOMED CT concepts: 698870008, 303098002, 733637001, 733636005, 49748000, and 106 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.89?
E72.89 is linked to 3 UMLS Concept Unique Identifiers: C0268517, C4718780, C0029774. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.