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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- disorders of:
- •aromatic amino-acid metabolismE70
- •branched-chain amino-acid metabolismE71.0-E71.2
- •fatty-acid metabolismE71.3
- •purine and pyrimidine metabolismE79
- •gout (M1A.-,M10
Related Codes(1)
Also Known As / Clinical Terms(437)
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
UMLS
Clinical Terms
- Disorder of the gamma-glutamyl cycle (disorder)
- Deficiency of phosphoserine phosphatase
- Deficiency of cysteine aminotransferase
- Deficiency of L-asparagine amidohydrolase
- Deficiency of acid-aminoacid ligase
- Deficiency of SGPT (serum glutamic pyruvic transaminase)
- Disorder of serine metabolism
- Combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia
- Deficiency of alanine dehydrogenase
- Deficiency of aminotransferase
- Deficiency of asparaginase
- Deficiency of alanine aminotransferase
- SSADH (succinic semialdehyde dehydrogenase) deficiency
- Spastic ataxia, dysarthria due to glutaminase deficiency
- Deficiency of GOT (glutamate oxaloacetate transaminase)
- Deficiency of glycine hydroxymethyltransferase
- Succinic semialdehyde dehydrogenase deficiency
- Deficiency of aminoacyl-histidine dipeptidase
- Congenital porphyria
- Aminoacidaemia
- Deficiency of hexosephosphate aminotransferase
- Disorder of GABA (gamma aminobutyric acid) metabolism
- Deficiency of protaminase
- Deficiency of threonine dehydratase
- Disorder of gamma-glutamyl cycle
- Deficiency of asparagine-oxo-acid aminotransferase
- HIBADH-gene related deficiency of 3-hydroxyisobutyrate dehydrogenase
- Deficiency of serine aldolase
- Deficiency of aspartate kinase
- Aminoacidemia
- Hyperprolinaemia
- Hyper-beta-alaninemia
- Pipecolic acidemia
- Disorder of creatine synthesis
- Deficiency of cystine reductase (NADH)
- 5-Oxoprolinase deficiency
- Deficiency of glutamine-oxo-acid transaminase
- Aminoacylase 1 deficiency
- Protoporphyria
- Deficiency of aspartate 4-decarboxylase
- Gamma-glutamyl transferase deficiency
- Deficiency of desulphinase
- Ferrochelatase deficiency
- Deficiency of L-serine deaminase
- Deficiency of glutamic-alanine transaminase
- D,L-2-hydroxyglutaric acidemia
- 2-hydroxyglutaric aciduria
- Deficiency of betaine-homocysteine methyltransferase
- Disorder of proline and hydroxyproline metabolism
- GABAuria
- Disorder of gamma-aminobutyric acid metabolism
- Deficiency of homoserine kinase
- Deficiency of guanidinoacetate methyltransferase
- Alaninemia
- Deficiency of threonine aldolase
- Deficiency of ophio-amino acid oxidase
- Disorder of glutamine metabolism
- Deficiency of alanyl-tRNA synthetase
- Deficiency of malonate CoA-transferase
- Deficiency of D-amino-acid oxidase
- Inborn error of glutathione metabolism
- Dicarboxylic aminoaciduria syndrome
- Deficiency of glutamic-aspartic transaminase
- Deficiency of glutaminase II
- Hyperprolinemia
- Deficiency of cysteine carboxypeptidase
- Glutamate aspartate transport defect
- FECH - Ferrochelatase deficiency
- Gamma-hydroxybutyric acidemia
- Deficiency of serine hydroxymethylase
- Deficiency of 3-hydroxyisobutyrate dehydrogenase
- Glutathionuria
- Alaninaemia
- Deficiency of L-asparaginase
- Guanidinoacetate methyltransferase deficiency
- 3-phosphoglycerate dehydrogenase deficiency juvenile form
- Disorder of proline AND/OR hydroxyproline metabolism
- Deficiency of serine-transfer ribonucleic acid ligase
- Deficiency of transaminase
- Erythrohepatic protoporphyria
- Deficiency of glutamine phenylacetyltransferase
- Glutathionaemia
- Hydroxyprolinemia
- Deficiency of serine deaminase
- Hyper-beta-carnosinaemia
- Glutathione synthetase deficiency
- Deficiency of D-aspartate oxidase
- Deficiency of glutamic-oxaloacetic transaminase
- Glutathionemia
- Deficiency of glycine amidinotransferase
- 5-Oxoprolinuria
- Camptodactyly of finger
- Alpha ketoadipic aciduria
- Disorder of threonine metabolism
- EPP - erythropoietic protoporphyria
- Inherited aminoaciduria
- Deficiency of ammonia-lyase
- Homocarnosinosis
- Prolinuria
- Pyroglutamicaciduria
- Neonatal epileptic encephalopathy due to glutaminase deficiency
- Serine biosynthesis pathway deficiency, infantile/juvenile form
- Disturbance of threonine metabolism
- Deficiency of pyrroline-5-carboxylate reductase
- Hyper-beta-carnosinemia
- Hyperhydroxyprolinemia
- Deficiency of betaine-aldehyde dehydrogenase
- Succinate-semialdehyde dehydrogenase deficiency
- Deficiency of glutamine synthetase
- Hyperhydroxyprolinaemia
- Deficiency of aminopeptidase
- Hyperdicarboxylicaminoaciduria AND hyperprolinemia
- Disorder of gamma aminobutyric acid metabolism
- Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerizing)
- Dibasic aminoaciduria
- 3-Phosphoglycerate dehydrogenase deficiency
- Deficiency of glucosamine-6-phosphate isomerase (glutamine-forming)
- Deficiency of carboxy-lyase
- Deficiency of aspartokinase
- Deficiency of glutamate decarboxylase
- Deficiency of peptide synthase
- Deficiency of cystine reductase (reduced nicotinamide adenine dinucleotide)
- Hereditary camptodactyly
- Deficiency of decarboxylase
- Iminoacidopathy
- Disorder of tetrahydrobiopterin metabolism
- Haem synthase deficiency
- Gamma-glutamylcysteine synthetase deficiency
- 4-Hydroxybutyric aciduria
- Hyperalaninaemia
- Congenital lysinuria
- Deficiency of adenosylhomocysteinase
- Combined D-2-hydroxyglutaric acidaemia and L-2-hydroxyglutaric acidaemia
- Deficiency of carboxypolypeptidase
- Hyperalaninemia
- Deficiency of GPT (glutamic pyruvic transaminase)
- Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
- Deficiency of alanine-transfer ribonucleic acid ligase
- Deficiency of aspartate aminotransferase
- Disturbance of glutamine metabolism
- Erythrocyte glutathione synthase deficiency
- Hydroxyprolinaemia
- Gamma-hydroxybutyric acidaemia
- Deficiency of SGOT (serum glutamic-oxaloacetic transaminase)
- Deficiency of threonine deaminase
- Glutamate-cysteine ligase deficiency
- Deficiency of serine carboxypeptidase
- Deficiency of aminoacylase 1
- Gamma-glutamyl transpeptidase deficiency
- Deficiency of carboxypeptidase B
- Deficiency of threonyl-tRNA synthetase
- Deficiency of alanine-tRNA ligase
- Heme synthase deficiency
- Disorder of beta and omega amino acid metabolism
- Deficiency of carnosinase
- Familial streblodactyly with amino-aciduria
- Camptodactyly taurinuria syndrome
- Glutathione synthase deficiency with 5-oxoprolinuria
- Glutathione synthase deficiency without 5-oxoprolinuria
- Deficiency of phosphoserine aminotransferase
- Deficiency of L-serine dehydratase
- Deficiency of glutamine-pyruvate aminotransferase
- Deficiency of glutamate-ammonia ligase
- Glycoprolinuria
- gamma-Hydroxybutyric aciduria
- Pipecolic acidaemia
- Deficiency of guanidinoacetate kinase
- delta'-Pyrroline-5-carboxylate dehydrogenase deficiency
- Deficiency of N-methyl-L-amino-acid oxidase
- GABA metabolic defect
- Lysinuric protein intolerance
- Deficiency of choline phosphatase
- Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism
- Deficiency of 4-hydroxy-2-oxoglutarate aldolase
- Deficiency of L-amino-acid oxidase
- Deficiency of glutaminase
- Pyroglutamate hydrolase deficiency
- Deficiency of threonine-tRNA ligase
- Deficiency of carboxypeptidase A
- Deficiency of hydrolase
- Deficiency of alanine-oxo-acid aminotransferase
- Deficiency of threonine-transfer ribonucleic acid ligase
- D,L-2-hydroxyglutaric acidaemia
- Deficiency of glutamate-cysteine ligase
- Hyperdibasic aminoaciduria
- Deficiency of aminoacyltransferase
- Disorder of the gamma-glutamyl cycle
- 3-phosphoglycerate dehydrogenase deficiency infantile form
- Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerising)
- Pyrroline-5-carboxylate reductase deficiency
- Disorders of beta-amino-acid metabolism
- Gamma-glutamyl cysteine synthase deficiency
- Deficiency of desulfinase
- Disorder of phenylalanine metabolism
- Neonatal epileptic encephalopathy due to deficiency of glutaminase
- Hyperdicarboxylicaminoaciduria AND hyperprolinaemia
- Deficiency of glutamate dehydrogenase
- Homocarnosinase deficiency
- Magnus syndrome
- Deficiency of cysteinyl-glycine dipeptidase
- Deficiency of glutamine transaminase L
- Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
- Hyper-beta-alaninaemia
- LPI - Lysinuric protein intolerance
- Disorders of gamma-glutamyl cycle
- Deficiency of cysteine proteinase
- Deficiency of seryl-tRNA synthetase
- Deficiency of cysteamine dioxygenase
- Deficiency of L-hydroxyaminoacid dehydratase
- Deficiency of 2-oxo-4-hydroxyglutarate aldolase
- Deficiency of serine-tRNA ligase
- Erythropoietic protoporphyria
- Deficiency of L-serine ammonia-lyase
- Phosphoserine aminotransferase deficiency
- Deficiency of glutamic dehydrogenase
- Deficiency of choline dehydrogenase
- Pyroglutamic aciduria
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.
How does E72.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified disorders of amino-acid metabolism affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E72.89?
There is no direct ICD-11 mapping available for E72.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.