E72.8 Deficiency of L-serine dehydratase

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Deficiency of L-serine dehydratase

Deficiency of L-serine dehydratase
Synonym for Other specified disorders of amino-acid metabolism

    E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E72 Other disorders of amino-acid metabolism

Results for Deficiency of L-serine dehydratase and additional synonyms


E72.8
Other specified disorders of amino-acid metabolism

Synonyms:

3-Phosphoglycerate dehydrogenase deficiency|3-Phosphoglycerate dehydrogenase deficiency (disorder)|4--Hydroxybutyric aciduria|5-Oxoprolinase deficiency|5-Oxoprolinase deficiency (disorder)|5-Oxoprolinuria|Alaninaemia|Alaninemia|Alaninemia (disorder)|Alpha ketoadipic aciduria|Alpha ketoadipic aciduria (disorder)|Aminoacidaemia|Aminoacidemia|Aminoacidemia (disorder)|Aminoacylase 1 deficiency|Arginine:glycine amidinotransferase deficiency|Benign neonatal hyperaminoaciduria|Benign neonatal hyperaminoaciduria (disorder)|Cerebral creatine deficiency syndrome 3|Cerebral creatine deficiency syndrome 3 (disorder)|Creatine deficiency syndrome due to arginine:glycine amidinotransferase deficiency|Deficiency of 2-oxo-4-hydroxyglutarate aldolase|Deficiency of 3-hydroxyisobutyrate dehydrogenase|Deficiency of 3-hydroxyisobutyrate dehydrogenase (disorder)|Deficiency of 4-hydroxy-2-oxoglutarate aldolase|Deficiency of 4-hydroxy-2-oxoglutarate aldolase (disorder)|Deficiency of A-ase|Deficiency of A-ase (disorder)|Deficiency of ASN-ase|Deficiency of D-amino-acid oxidase|Deficiency of D-amino-acid oxidase (disorder)|Deficiency of D-aspartate oxidase|Deficiency of D-aspartate oxidase (disorder)|Deficiency of GOT|Deficiency of GPT|Deficiency of L-amino-acid oxidase|Deficiency of L-amino-acid oxidase (disorder)|Deficiency of L-asparaginase|Deficiency of L-asparagine amidohydrolase|Deficiency of L-asparagine amidohydrolase (disorder)|Deficiency of L-hydroxyaminoacid dehydratase|Deficiency of L-serine dehydratase|Deficiency of L-serine dehydratase (disorder)|Deficiency of N-methyl-L-amino-acid oxidase|Deficiency of N-methyl-L-amino-acid oxidase (disorder)|Deficiency of SGOT|Deficiency of SGPT|Deficiency of acid-aminoacid ligase|Deficiency of acid-aminoacid ligase (disorder)|Deficiency of adenosylhomocysteinase|Deficiency of adenosylhomocysteinase (disorder)|Deficiency of alanine aminotransferase|Deficiency of alanine aminotransferase (disorder)|Deficiency of alanine dehydrogenase|Deficiency of alanine dehydrogenase (disorder)|Deficiency of alanine-oxo-acid aminotransferase|Deficiency of alanine-oxo-acid aminotransferase (disorder)|Deficiency of alanine-tRNA ligase|Deficiency of alanine-transfer ribonucleic acid ligase|Deficiency of alanine-transfer ribonucleic acid ligase (disorder)|Deficiency of alanyl-tRNA synthetase|Deficiency of aminoacyl-histidine dipeptidase|Deficiency of aminoacyl-histidine dipeptidase (disorder)|Deficiency of aminoacylase 1|Deficiency of aminoacylase 1 (disorder)|Deficiency of aminoacyltransferase|Deficiency of aminoacyltransferase (disorder)|Deficiency of aminopeptidase|Deficiency of aminopeptidase (disorder)|Deficiency of aminotransferase|Deficiency of aminotransferase (disorder)|Deficiency of ammonia-lyase|Deficiency of ammonia-lyase (disorder)|Deficiency of asparaginase|Deficiency of asparaginase II|Deficiency of asparagine-oxo-acid aminotransferase|Deficiency of asparagine-oxo-acid aminotransferase (disorder)|Deficiency of aspartate 4-decarboxylase|Deficiency of aspartate 4-decarboxylase (disorder)|Deficiency of aspartate aminotransferase|Deficiency of aspartate aminotransferase (disorder)|Deficiency of aspartate kinase|Deficiency of aspartate kinase (disorder)|Deficiency of aspartokinase|Deficiency of betaine-aldehyde dehydrogenase|Deficiency of betaine-aldehyde dehydrogenase (disorder)|Deficiency of betaine-homocysteine methyltransferase|Deficiency of betaine-homocysteine methyltransferase (disorder)|Deficiency of carboxy-lyase|Deficiency of carboxy-lyase (disorder)|Deficiency of carboxypeptidase A|Deficiency of carboxypeptidase A (disorder)|Deficiency of carboxypeptidase B|Deficiency of carboxypeptidase B (disorder)|Deficiency of carboxypolypeptidase|Deficiency of carnosinase|Deficiency of carnosinase (disorder)|Deficiency of choline dehydrogenase|Deficiency of choline dehydrogenase (disorder)|Deficiency of choline phosphatase|Deficiency of cysteamine dioxygenase|Deficiency of cysteamine dioxygenase (disorder)|Deficiency of cysteine aminotransferase|Deficiency of cysteine aminotransferase (disorder)|Deficiency of cysteine carboxypeptidase|Deficiency of cysteine carboxypeptidase (disorder)|Deficiency of cysteine proteinase|Deficiency of cysteine proteinase (disorder)|Deficiency of cysteinyl-glycine dipeptidase|Deficiency of cysteinyl-glycine dipeptidase (disorder)|Deficiency of cystine reductase (NADH)|Deficiency of cystine reductase (reduced nicotinamide adenine dinucleotide)|Deficiency of cystine reductase (reduced nicotinamide adenine dinucleotide) (disorder)|Deficiency of cytosol aminopeptidase|Deficiency of cytosol aminopeptidase (disorder)|Deficiency of decarboxylase|Deficiency of desulfinase|Deficiency of desulphinase|Deficiency of glucosamine-6-phosphate isomerase (glutamine-forming)|Deficiency of glutamate decarboxylase|Deficiency of glutamate decarboxylase (disorder)|Deficiency of glutamate dehydrogenase|Deficiency of glutamate dehydrogenase (disorder)|Deficiency of glutamate-ammonia ligase|Deficiency of glutamate-ammonia ligase (disorder)|Deficiency of glutamate-cysteine ligase|Deficiency of glutamic dehydrogenase|Deficiency of glutamic-alanine transaminase|Deficiency of glutamic-aspartic transaminase|Deficiency of glutamic-oxaloacetic transaminase|Deficiency of glutaminase|Deficiency of glutaminase (disorder)|Deficiency of glutaminase II|Deficiency of glutamine phenylacetyltransferase|Deficiency of glutamine phenylacetyltransferase (disorder)|Deficiency of glutamine synthetase|Deficiency of glutamine transaminase L|Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerising)|Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerizing)|Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerizing) (disorder)|Deficiency of glutamine-oxo-acid transaminase|Deficiency of glutamine-pyruvate aminotransferase|Deficiency of glutamine-pyruvate aminotransferase (disorder)|Deficiency of glycine amidinotransferase|Deficiency of glycine amidinotransferase (disorder)|Deficiency of glycine hydroxymethyltransferase|Deficiency of glycine hydroxymethyltransferase (disorder)|Deficiency of guanidinoacetate kinase|Deficiency of guanidinoacetate kinase (disorder)|Deficiency of guanidinoacetate methyltransferase|Deficiency of guanidinoacetate methyltransferase (disorder)|Deficiency of hexosephosphate aminotransferase|Deficiency of homoserine kinase|Deficiency of homoserine kinase (disorder)|Deficiency of malonate CoA-transferase|Deficiency of malonate CoA-transferase (disorder)|Deficiency of ophio-amino acid oxidase|Deficiency of peptide synthase|Deficiency of phosphoserine phosphatase|Deficiency of phosphoserine phosphatase (disorder)|Deficiency of proline dipeptidase|Deficiency of proline dipeptidase (disorder)|Deficiency of protaminase|Deficiency of pyrroline-5-carboxylate reductase|Deficiency of pyrroline-5-carboxylate reductase (disorder)|Deficiency of serine aldolase|Deficiency of serine carboxypeptidase|Deficiency of serine carboxypeptidase (disorder)|Deficiency of serine deaminase|Deficiency of serine hydroxymethylase|Deficiency of serine-tRNA ligase|Deficiency of serine-transfer ribonucleic acid ligase|Deficiency of serine-transfer ribonucleic acid ligase (disorder)|Deficiency of seryl-tRNA synthetase|Deficiency of threonine aldolase|Deficiency of threonine aldolase (disorder)|Deficiency of threonine deaminase|Deficiency of threonine dehydratase|Deficiency of threonine dehydratase (disorder)|Deficiency of threonine-tRNA ligase|Deficiency of threonine-transfer ribonucleic acid ligase|Deficiency of threonine-transfer ribonucleic acid ligase (disorder)|Deficiency of threonyl-tRNA synthetase|Deficiency of transaminase|Dibasic aminoaciduria|Dibasic aminoaciduria (disorder)|Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism|Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism (disorder)|Disorder of beta and omega amino acid metabolism|Disorder of beta and omega amino acid metabolism (disorder)|Disorder of creatine synthesis|Disorder of creatine synthesis (disorder)|Disorder of gamma-glutamyl cycle|Disorder of glutamine metabolism|Disorder of glutamine metabolism (disorder)|Disorder of phenylalanine metabolism|Disorder of phenylalanine metabolism (disorder)|Disorder of proline AND/OR hydroxyproline metabolism|Disorder of proline AND/OR hydroxyproline metabolism (disorder)|Disorder of proline and hydroxyproline metabolism|Disorder of serine metabolism|Disorder of serine metabolism (disorder)|Disorder of tetrahydrobiopterin metabolism|Disorder of tetrahydrobiopterin metabolism (disorder)|Disorder of the gamma-glutamyl cycle|Disorder of the gamma-glutamyl cycle (disorder)|Disorder of threonine metabolism|Disorder of threonine metabolism (disorder)|Disorders of beta-amino-acid metabolism|Disorders of gamma-glutamyl cycle|Disturbance of glutamine metabolism|Disturbance of threonine metabolism|Erythrocyte glutathione synthase deficiency|GABA metabolic defect|GABAuria|Gamma-aminobutyric acid transaminase deficiency|Gamma-aminobutyric acid transaminase deficiency (disorder)|Gamma-glutamyl cysteine synthase deficiency|Gamma-glutamyl transpeptidase deficiency|Gamma-glutamylcysteine synthetase deficiency|Gamma-hydroxybutyric acidaemia|Gamma-hydroxybutyric acidemia|Glucoaminophosphaturia syndrome with rickets|Glucoaminophosphaturia syndrome with rickets (disorder)|Glutamate-cysteine ligase deficiency|Glutamate-cysteine ligase deficiency (disorder)|Glutathionaemia|Glutathione synthase deficiency with 5-oxoprolinuria|Glutathione synthase deficiency with 5-oxoprolinuria (disorder)|Glutathione synthase deficiency without 5-oxoprolinuria|Glutathione synthase deficiency without 5-oxoprolinuria (disorder)|Glutathionemia|Glutathionemia (disorder)|Glutathioninuria|Glycoprolinuria|Glycoprolinuria (disorder)|Guanidinoacetate methyltransferase deficiency|Homocarnosinase deficiency|Homocarnosinase deficiency (disorder)|Homocarnosinosis|Hydroxyprolinaemia|Hydroxyprolinemia|Hyper-beta-alaninaemia|Hyper-beta-alaninemia|Hyper-beta-alaninemia (disorder)|Hyper-beta-carnosinaemia|Hyper-beta-carnosinemia|Hyper-beta-carnosinemia (disorder)|Hyperalaninaemia|Hyperalaninemia|Hyperdicarboxylicaminoaciduria AND hyperprolinaemia|Hyperdicarboxylicaminoaciduria AND hyperprolinemia|Hyperdicarboxylicaminoaciduria AND hyperprolinemia (disorder)|Hyperhydroxyprolinaemia|Hyperhydroxyprolinemia|Hyperhydroxyprolinemia (disorder)|Hyperprolinaemia type II|Hyperprolinaemia, type II|Hyperprolinemia type II|Hyperprolinemia, type II|Iminoacidopathy|Iminoacidopathy (disorder)|Inborn error of glutathione metabolism|Inborn error of glutathione metabolism (disorder)|L-arginine:glycine amidinotransferase deficiency|Pipecolic acidaemia|Pipecolic acidemia|Pipecolic acidemia (disorder)|Prolinuria|Prolinuria (disorder)|Pyroglutamate hydrolase deficiency|Pyroglutamic acidaemia|Pyroglutamic acidemia|Pyroglutamic aciduria|Pyrroline-5-carboxylate reductase deficiency|Succinate-semialdehyde dehydrogenase deficiency|Succinate-semialdehyde dehydrogenase deficiency (disorder)|Succinic semialdehyde dehydrogenase deficiency|delta'-Pyrroline-5-carboxylate dehydrogenase deficiency|gamma-Glutamyl transpeptidase deficiency|gamma-Glutamyltransferase deficiency|gamma-Glutamyltransferase deficiency (disorder)|gamma-Hydroxybutyric aciduria

Subcategories:

    All content of the ICD-10 CM Search is based on the classifications and codes of the Centers for Medicare and Medicaid Services (CMS) and the National Center for Health Statistics (NCHS). The accumulation of synonyms is carried out by Averbis GmbH with Healthcare Natural Language Processing. All information is provided without guarantee. Errors and omissions excepted. We expressly reserve the right to make changes, additions or deletions to the information or links provided at any time without prior notice. Our offer is non-binding. For correctness, completeness and topicality or designations no liability is assumed.

    ICD-Search ICD 10 CM (Clinical Modification) 2017 through Healthcare Natural Language Processing & Deep Learning

    ICD-Code / International Statistical Classification of Diseases and Related Health Problems (ICD) for: Deficiency of L-serine dehydratase

    ICD Code for Disease, Diagnosis E72.8

    ICD Code an Classification Other specified disorders of amino-acid metabolism

    Chapter, Outline, Main Categories, Parent Concepts or Top Concepts: E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E72 Other disorders of amino-acid metabolism

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: E72.8: Deficiency of L-serine dehydratase

    Other Synonyms of the Category: 3-Phosphoglycerate dehydrogenase deficiency|3-Phosphoglycerate dehydrogenase deficiency (disorder)|4--Hydroxybutyric aciduria|5-Oxoprolinase deficiency|5-Oxoprolinase deficiency (disorder)|5-Oxoprolinuria|Alaninaemia|Alaninemia|Alaninemia (disorder)|Alpha ketoadipic aciduria|Alpha ketoadipic aciduria (disorder)|Aminoacidaemia|Aminoacidemia|Aminoacidemia (disorder)|Aminoacylase 1 deficiency|Arginine:glycine amidinotransferase deficiency|Benign neonatal hyperaminoaciduria|Benign neonatal hyperaminoaciduria (disorder)|Cerebral creatine deficiency syndrome 3|Cerebral creatine deficiency syndrome 3 (disorder)|Creatine deficiency syndrome due to arginine:glycine amidinotransferase deficiency|Deficiency of 2-oxo-4-hydroxyglutarate aldolase|Deficiency of 3-hydroxyisobutyrate dehydrogenase|Deficiency of 3-hydroxyisobutyrate dehydrogenase (disorder)|Deficiency of 4-hydroxy-2-oxoglutarate aldolase|Deficiency of 4-hydroxy-2-oxoglutarate aldolase (disorder)|Deficiency of A-ase|Deficiency of A-ase (disorder)|Deficiency of ASN-ase|Deficiency of D-amino-acid oxidase|Deficiency of D-amino-acid oxidase (disorder)|Deficiency of D-aspartate oxidase|Deficiency of D-aspartate oxidase (disorder)|Deficiency of GOT|Deficiency of GPT|Deficiency of L-amino-acid oxidase|Deficiency of L-amino-acid oxidase (disorder)|Deficiency of L-asparaginase|Deficiency of L-asparagine amidohydrolase|Deficiency of L-asparagine amidohydrolase (disorder)|Deficiency of L-hydroxyaminoacid dehydratase|Deficiency of L-serine dehydratase|Deficiency of L-serine dehydratase (disorder)|Deficiency of N-methyl-L-amino-acid oxidase|Deficiency of N-methyl-L-amino-acid oxidase (disorder)|Deficiency of SGOT|Deficiency of SGPT|Deficiency of acid-aminoacid ligase|Deficiency of acid-aminoacid ligase (disorder)|Deficiency of adenosylhomocysteinase|Deficiency of adenosylhomocysteinase (disorder)|Deficiency of alanine aminotransferase|Deficiency of alanine aminotransferase (disorder)|Deficiency of alanine dehydrogenase|Deficiency of alanine dehydrogenase (disorder)|Deficiency of alanine-oxo-acid aminotransferase|Deficiency of alanine-oxo-acid aminotransferase (disorder)|Deficiency of alanine-tRNA ligase|Deficiency of alanine-transfer ribonucleic acid ligase|Deficiency of alanine-transfer ribonucleic acid ligase (disorder)|Deficiency of alanyl-tRNA synthetase|Deficiency of aminoacyl-histidine dipeptidase|Deficiency of aminoacyl-histidine dipeptidase (disorder)|Deficiency of aminoacylase 1|Deficiency of aminoacylase 1 (disorder)|Deficiency of aminoacyltransferase|Deficiency of aminoacyltransferase (disorder)|Deficiency of aminopeptidase|Deficiency of aminopeptidase (disorder)|Deficiency of aminotransferase|Deficiency of aminotransferase (disorder)|Deficiency of ammonia-lyase|Deficiency of ammonia-lyase (disorder)|Deficiency of asparaginase|Deficiency of asparaginase II|Deficiency of asparagine-oxo-acid aminotransferase|Deficiency of asparagine-oxo-acid aminotransferase (disorder)|Deficiency of aspartate 4-decarboxylase|Deficiency of aspartate 4-decarboxylase (disorder)|Deficiency of aspartate aminotransferase|Deficiency of aspartate aminotransferase (disorder)|Deficiency of aspartate kinase|Deficiency of aspartate kinase (disorder)|Deficiency of aspartokinase|Deficiency of betaine-aldehyde dehydrogenase|Deficiency of betaine-aldehyde dehydrogenase (disorder)|Deficiency of betaine-homocysteine methyltransferase|Deficiency of betaine-homocysteine methyltransferase (disorder)|Deficiency of carboxy-lyase|Deficiency of carboxy-lyase (disorder)|Deficiency of carboxypeptidase A|Deficiency of carboxypeptidase A (disorder)|Deficiency of carboxypeptidase B|Deficiency of carboxypeptidase B (disorder)|Deficiency of carboxypolypeptidase|Deficiency of carnosinase|Deficiency of carnosinase (disorder)|Deficiency of choline dehydrogenase|Deficiency of choline dehydrogenase (disorder)|Deficiency of choline phosphatase|Deficiency of cysteamine dioxygenase|Deficiency of cysteamine dioxygenase (disorder)|Deficiency of cysteine aminotransferase|Deficiency of cysteine aminotransferase (disorder)|Deficiency of cysteine carboxypeptidase|Deficiency of cysteine carboxypeptidase (disorder)|Deficiency of cysteine proteinase|Deficiency of cysteine proteinase (disorder)|Deficiency of cysteinyl-glycine dipeptidase|Deficiency of cysteinyl-glycine dipeptidase (disorder)|Deficiency of cystine reductase (NADH)|Deficiency of cystine reductase (reduced nicotinamide adenine dinucleotide)|Deficiency of cystine reductase (reduced nicotinamide adenine dinucleotide) (disorder)|Deficiency of cytosol aminopeptidase|Deficiency of cytosol aminopeptidase (disorder)|Deficiency of decarboxylase|Deficiency of desulfinase|Deficiency of desulphinase|Deficiency of glucosamine-6-phosphate isomerase (glutamine-forming)|Deficiency of glutamate decarboxylase|Deficiency of glutamate decarboxylase (disorder)|Deficiency of glutamate dehydrogenase|Deficiency of glutamate dehydrogenase (disorder)|Deficiency of glutamate-ammonia ligase|Deficiency of glutamate-ammonia ligase (disorder)|Deficiency of glutamate-cysteine ligase|Deficiency of glutamic dehydrogenase|Deficiency of glutamic-alanine transaminase|Deficiency of glutamic-aspartic transaminase|Deficiency of glutamic-oxaloacetic transaminase|Deficiency of glutaminase|Deficiency of glutaminase (disorder)|Deficiency of glutaminase II|Deficiency of glutamine phenylacetyltransferase|Deficiency of glutamine phenylacetyltransferase (disorder)|Deficiency of glutamine synthetase|Deficiency of glutamine transaminase L|Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerising)|Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerizing)|Deficiency of glutamine-fructose-6-phosphate aminotransferase (isomerizing) (disorder)|Deficiency of glutamine-oxo-acid transaminase|Deficiency of glutamine-pyruvate aminotransferase|Deficiency of glutamine-pyruvate aminotransferase (disorder)|Deficiency of glycine amidinotransferase|Deficiency of glycine amidinotransferase (disorder)|Deficiency of glycine hydroxymethyltransferase|Deficiency of glycine hydroxymethyltransferase (disorder)|Deficiency of guanidinoacetate kinase|Deficiency of guanidinoacetate kinase (disorder)|Deficiency of guanidinoacetate methyltransferase|Deficiency of guanidinoacetate methyltransferase (disorder)|Deficiency of hexosephosphate aminotransferase|Deficiency of homoserine kinase|Deficiency of homoserine kinase (disorder)|Deficiency of malonate CoA-transferase|Deficiency of malonate CoA-transferase (disorder)|Deficiency of ophio-amino acid oxidase|Deficiency of peptide synthase|Deficiency of phosphoserine phosphatase|Deficiency of phosphoserine phosphatase (disorder)|Deficiency of proline dipeptidase|Deficiency of proline dipeptidase (disorder)|Deficiency of protaminase|Deficiency of pyrroline-5-carboxylate reductase|Deficiency of pyrroline-5-carboxylate reductase (disorder)|Deficiency of serine aldolase|Deficiency of serine carboxypeptidase|Deficiency of serine carboxypeptidase (disorder)|Deficiency of serine deaminase|Deficiency of serine hydroxymethylase|Deficiency of serine-tRNA ligase|Deficiency of serine-transfer ribonucleic acid ligase|Deficiency of serine-transfer ribonucleic acid ligase (disorder)|Deficiency of seryl-tRNA synthetase|Deficiency of threonine aldolase|Deficiency of threonine aldolase (disorder)|Deficiency of threonine deaminase|Deficiency of threonine dehydratase|Deficiency of threonine dehydratase (disorder)|Deficiency of threonine-tRNA ligase|Deficiency of threonine-transfer ribonucleic acid ligase|Deficiency of threonine-transfer ribonucleic acid ligase (disorder)|Deficiency of threonyl-tRNA synthetase|Deficiency of transaminase|Dibasic aminoaciduria|Dibasic aminoaciduria (disorder)|Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism|Disorder of beta alanine, carnosine AND/OR homocarnosine metabolism (disorder)|Disorder of beta and omega amino acid metabolism|Disorder of beta and omega amino acid metabolism (disorder)|Disorder of creatine synthesis|Disorder of creatine synthesis (disorder)|Disorder of gamma-glutamyl cycle|Disorder of glutamine metabolism|Disorder of glutamine metabolism (disorder)|Disorder of phenylalanine metabolism|Disorder of phenylalanine metabolism (disorder)|Disorder of proline AND/OR hydroxyproline metabolism|Disorder of proline AND/OR hydroxyproline metabolism (disorder)|Disorder of proline and hydroxyproline metabolism|Disorder of serine metabolism|Disorder of serine metabolism (disorder)|Disorder of tetrahydrobiopterin metabolism|Disorder of tetrahydrobiopterin metabolism (disorder)|Disorder of the gamma-glutamyl cycle|Disorder of the gamma-glutamyl cycle (disorder)|Disorder of threonine metabolism|Disorder of threonine metabolism (disorder)|Disorders of beta-amino-acid metabolism|Disorders of gamma-glutamyl cycle|Disturbance of glutamine metabolism|Disturbance of threonine metabolism|Erythrocyte glutathione synthase deficiency|GABA metabolic defect|GABAuria|Gamma-aminobutyric acid transaminase deficiency|Gamma-aminobutyric acid transaminase deficiency (disorder)|Gamma-glutamyl cysteine synthase deficiency|Gamma-glutamyl transpeptidase deficiency|Gamma-glutamylcysteine synthetase deficiency|Gamma-hydroxybutyric acidaemia|Gamma-hydroxybutyric acidemia|Glucoaminophosphaturia syndrome with rickets|Glucoaminophosphaturia syndrome with rickets (disorder)|Glutamate-cysteine ligase deficiency|Glutamate-cysteine ligase deficiency (disorder)|Glutathionaemia|Glutathione synthase deficiency with 5-oxoprolinuria|Glutathione synthase deficiency with 5-oxoprolinuria (disorder)|Glutathione synthase deficiency without 5-oxoprolinuria|Glutathione synthase deficiency without 5-oxoprolinuria (disorder)|Glutathionemia|Glutathionemia (disorder)|Glutathioninuria|Glycoprolinuria|Glycoprolinuria (disorder)|Guanidinoacetate methyltransferase deficiency|Homocarnosinase deficiency|Homocarnosinase deficiency (disorder)|Homocarnosinosis|Hydroxyprolinaemia|Hydroxyprolinemia|Hyper-beta-alaninaemia|Hyper-beta-alaninemia|Hyper-beta-alaninemia (disorder)|Hyper-beta-carnosinaemia|Hyper-beta-carnosinemia|Hyper-beta-carnosinemia (disorder)|Hyperalaninaemia|Hyperalaninemia|Hyperdicarboxylicaminoaciduria AND hyperprolinaemia|Hyperdicarboxylicaminoaciduria AND hyperprolinemia|Hyperdicarboxylicaminoaciduria AND hyperprolinemia (disorder)|Hyperhydroxyprolinaemia|Hyperhydroxyprolinemia|Hyperhydroxyprolinemia (disorder)|Hyperprolinaemia type II|Hyperprolinaemia, type II|Hyperprolinemia type II|Hyperprolinemia, type II|Iminoacidopathy|Iminoacidopathy (disorder)|Inborn error of glutathione metabolism|Inborn error of glutathione metabolism (disorder)|L-arginine:glycine amidinotransferase deficiency|Pipecolic acidaemia|Pipecolic acidemia|Pipecolic acidemia (disorder)|Prolinuria|Prolinuria (disorder)|Pyroglutamate hydrolase deficiency|Pyroglutamic acidaemia|Pyroglutamic acidemia|Pyroglutamic aciduria|Pyrroline-5-carboxylate reductase deficiency|Succinate-semialdehyde dehydrogenase deficiency|Succinate-semialdehyde dehydrogenase deficiency (disorder)|Succinic semialdehyde dehydrogenase deficiency|delta'-Pyrroline-5-carboxylate dehydrogenase deficiency|gamma-Glutamyl transpeptidase deficiency|gamma-Glutamyltransferase deficiency|gamma-Glutamyltransferase deficiency (disorder)|gamma-Hydroxybutyric aciduria

    ICD 10 CM 2017, (Clinical Modification) for coding of death certificates and mortality data. The international Statistical Classification of Diseases and Related Health Problems (ICD) 10th Revision and Clinical Modification. International Classification of Diseases, Tenth Revision, Clinical Modification.E72.8 Other specified disorders of amino-acid metabolism and Deficiency of L-serine dehydratase

    Deficiency of L-serine dehydratase
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