E74.8 Essential pentosuria (disorder)

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Essential pentosuria (disorder)

Essential pentosuria (disorder)
Synonym for Other specified disorders of carbohydrate metabolism

    E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E74 Other disorders of carbohydrate metabolism

Results for Essential pentosuria (disorder) and additional synonyms


E74.8
Other specified disorders of carbohydrate metabolism

Synonyms:

ALG12-congenital disorder of glycosylation|ALG12-congenital disorder of glycosylation (disorder)|Alpha, alpha-trehalase deficiency|Carbohydrate deficient glycoprotein syndrome type 1c|Carbohydrate deficient glycoprotein syndrome type V|Congenital disorder of glycosylation type 1G|Congenital disorder of glycosylation type 1c|Congenital disorder of glycosylation type 1c (disorder)|Congenital disorder of glycosylation type Ig|D-Glyceric aciduria|D-Glyceric aciduria (disorder)|Deficiency of 6-alpha-D-glucosidase|Deficiency of ALR2|Deficiency of aldehyde reductase|Deficiency of aldehyde reductase (disorder)|Deficiency of aldonolactonase|Deficiency of aldonolactonase (disorder)|Deficiency of aldose 1-epimerase|Deficiency of aldose 1-epimerase (disorder)|Deficiency of aldose mutarotase|Deficiency of alpha-amylase|Deficiency of alpha-amylase (disorder)|Deficiency of alpha-mannosidase|Deficiency of alpha-mannosidase (disorder)|Deficiency of amygdalase|Deficiency of amylase|Deficiency of amylase (disorder)|Deficiency of amylo-1,6-glucosidase|Deficiency of amylo-1,6-glucosidase (disorder)|Deficiency of amylopectin 6-glucanohydrolase|Deficiency of amylopectin 6-glucanohydrolase (disorder)|Deficiency of benzaldehyde dehydrogenase (NADP^+^)|Deficiency of benzaldehyde dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^)|Deficiency of benzaldehyde dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) (disorder)|Deficiency of beta-amylase|Deficiency of beta-amylase (disorder)|Deficiency of beta-fructofuranosidase|Deficiency of beta-fructofuranosidase (disorder)|Deficiency of beta-glucosidase|Deficiency of beta-glucosidase (disorder)|Deficiency of beta-glucuronidase|Deficiency of beta-glucuronidase (disorder)|Deficiency of bisphosphoglycerate mutase|Deficiency of bisphosphoglycerate mutase (disorder)|Deficiency of bisphosphoglycerate phosphatase|Deficiency of bisphosphoglycerate phosphatase (disorder)|Deficiency of bisphosphoglycerate synthase|Deficiency of cellobiase|Deficiency of dextrin|Deficiency of diphosphoglycerate mutase|Deficiency of endo-1,3(4)-beta-glucanase|Deficiency of endo-1,3(4)-beta-glucanase (disorder)|Deficiency of endo-1,3-beta-glucanase|Deficiency of exo-1,3-alpha-glucanase|Deficiency of gentiobiase|Deficiency of glucan 1,3-alpha-glucosidase|Deficiency of glucan 1,3-alpha-glucosidase (disorder)|Deficiency of glucokinase|Deficiency of glucokinase (disorder)|Deficiency of gluconate 2-dehydrogenase|Deficiency of gluconate 2-dehydrogenase (disorder)|Deficiency of gluconokinase|Deficiency of gluconokinase (disorder)|Deficiency of gluconolactonase|Deficiency of gluconolactonase (disorder)|Deficiency of glucosamine-6-phosphate isomerase|Deficiency of glucosamine-6-phosphate isomerase (disorder)|Deficiency of glucose dehydrogenase|Deficiency of glucose dehydrogenase (disorder)|Deficiency of glucose oxidase|Deficiency of glucose oxidase (disorder)|Deficiency of glucose oxyhydrase|Deficiency of glucose-1-phosphatase|Deficiency of glucose-1-phosphatase (disorder)|Deficiency of glucose-6-phosphate isomerase|Deficiency of glucose-6-phosphate isomerase (disorder)|Deficiency of glucose-phosphate kinase|Deficiency of glucosulfatase|Deficiency of glucosulphatase|Deficiency of glucosyltransferase 1|Deficiency of glucosyltransferase 1 (disorder)|Deficiency of glyceraldehyde-3-phosphate dehydrogenase|Deficiency of glyceraldehyde-3-phosphate dehydrogenase (disorder)|Deficiency of glycerate phosphomutase|Deficiency of glycerol kinase|Deficiency of glycerol kinase (disorder)|Deficiency of glycogenase|Deficiency of glycosidase|Deficiency of glycosidase (disorder)|Deficiency of glycosulfatase|Deficiency of glycosulfatase (disorder)|Deficiency of glycosulphatase|Deficiency of glycosyltransferase|Deficiency of glycosyltransferase (disorder)|Deficiency of hexosephosphate isomerase|Deficiency of invertase|Deficiency of laminarinase|Deficiency of maltose phosphorylase|Deficiency of maltose phosphorylase (disorder)|Deficiency of mannokinase|Deficiency of mannokinase (disorder)|Deficiency of mutarotase|Deficiency of oxoisomerase|Deficiency of phosphoglucoisomerase|Deficiency of phosphoglucokinase|Deficiency of phosphoglucokinase (disorder)|Deficiency of phosphoglycerate kinase|Deficiency of phosphoglycerate kinase (disorder)|Deficiency of phosphohexose isomerase|Deficiency of phosphomannomutase 2|Deficiency of phosphomannomutase 2 (disorder)|Deficiency of phosphorylase b kinase|Deficiency of phosphorylase b kinase (disorder)|Deficiency of polyol dehydrogenase (NADP^+^)|Deficiency of rhamnulokinase|Deficiency of rhamnulokinase (disorder)|Deficiency of saccharase|Deficiency of saccharogen amylase|Deficiency of transglycosylase|Deficiency of triosephosphate dehydrogenase|Deficiency of xylulokinase|Deficiency of xylulokinase (disorder)|Disacchariduria|Disacchariduria (disorder)|Disorder of glucose metabolism|Disorder of glucose metabolism (disorder)|Disorder of glucose regulation|Disorder of glucose regulation (disorder)|Disorder of glycerate metabolism|Disorder of glycerate metabolism (disorder)|Disorder of glycerol metabolism|Disorder of glycerol metabolism (disorder)|Essential benign pentosuria|Essential pentosuria|Essential pentosuria (disorder)|Familial hyperglycerolaemia|Familial hyperglycerolemia|Familial renal glucosuria|Familial renal glucosuria (disorder)|GK1 deficiency|GKD - Glycerol kinase deficiency|GTT = renal glycosuria|Glucose tolerance test = renal glycosuria|Glucose tolerance test = renal glycosuria (finding)|Glycerol intolerance|Glycerol intolerance (disorder)|Glycerol kinase deficiency|Glycerol kinase deficiency - contiguous gene syndrome|Glycerol kinase deficiency - contiguous gene syndrome (disorder)|Glycerol kinase deficiency - isolated|Glycerol kinase deficiency - isolated (disorder)|Hyperglycerolaemia|Hyperglycerolemia|L-xylulose reductase deficiency|L-xylulosuria|Low renal threshold for glucose|Low renal threshold for glucose (disorder)|Muscle phosphoglycerate mutase deficiency|Muscle phosphoglycerate mutase deficiency (disorder)|Non glucose melituria|Nonglucosuric melituria|Nonglucosuric melituria (disorder)|Pentose disorder|Pentose disorder (disorder)|Phosphoglucomutase deficiency|Renal diabetes|Renal diabetes (disorder)|Renal glucosuria|Renal glucosuria, type A|Renal glucosuria, type A (disorder)|Renal glucosuria, type B|Renal glucosuria, type B (disorder)|Renal glucosuria, type O|Renal glucosuria, type O (disorder)|Renal glycosuria|Renal glycosuria (disorder)|Trehalase deficiency|Trehalose intolerance|Xylitol dehydrogenase deficiency|Xylosuria|Xylosuria (disorder)|alpha, alpha-Trehalase deficiency|alpha, alpha-Trehalase deficiency (disorder)

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: Essential pentosuria (disorder)

    ICD Code for Disease, Diagnosis E74.8

    ICD Code an Classification Other specified disorders of carbohydrate 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)|E74 Other disorders of carbohydrate metabolism

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: E74.8: Essential pentosuria (disorder)

    Other Synonyms of the Category: ALG12-congenital disorder of glycosylation|ALG12-congenital disorder of glycosylation (disorder)|Alpha, alpha-trehalase deficiency|Carbohydrate deficient glycoprotein syndrome type 1c|Carbohydrate deficient glycoprotein syndrome type V|Congenital disorder of glycosylation type 1G|Congenital disorder of glycosylation type 1c|Congenital disorder of glycosylation type 1c (disorder)|Congenital disorder of glycosylation type Ig|D-Glyceric aciduria|D-Glyceric aciduria (disorder)|Deficiency of 6-alpha-D-glucosidase|Deficiency of ALR2|Deficiency of aldehyde reductase|Deficiency of aldehyde reductase (disorder)|Deficiency of aldonolactonase|Deficiency of aldonolactonase (disorder)|Deficiency of aldose 1-epimerase|Deficiency of aldose 1-epimerase (disorder)|Deficiency of aldose mutarotase|Deficiency of alpha-amylase|Deficiency of alpha-amylase (disorder)|Deficiency of alpha-mannosidase|Deficiency of alpha-mannosidase (disorder)|Deficiency of amygdalase|Deficiency of amylase|Deficiency of amylase (disorder)|Deficiency of amylo-1,6-glucosidase|Deficiency of amylo-1,6-glucosidase (disorder)|Deficiency of amylopectin 6-glucanohydrolase|Deficiency of amylopectin 6-glucanohydrolase (disorder)|Deficiency of benzaldehyde dehydrogenase (NADP^+^)|Deficiency of benzaldehyde dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^)|Deficiency of benzaldehyde dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) (disorder)|Deficiency of beta-amylase|Deficiency of beta-amylase (disorder)|Deficiency of beta-fructofuranosidase|Deficiency of beta-fructofuranosidase (disorder)|Deficiency of beta-glucosidase|Deficiency of beta-glucosidase (disorder)|Deficiency of beta-glucuronidase|Deficiency of beta-glucuronidase (disorder)|Deficiency of bisphosphoglycerate mutase|Deficiency of bisphosphoglycerate mutase (disorder)|Deficiency of bisphosphoglycerate phosphatase|Deficiency of bisphosphoglycerate phosphatase (disorder)|Deficiency of bisphosphoglycerate synthase|Deficiency of cellobiase|Deficiency of dextrin|Deficiency of diphosphoglycerate mutase|Deficiency of endo-1,3(4)-beta-glucanase|Deficiency of endo-1,3(4)-beta-glucanase (disorder)|Deficiency of endo-1,3-beta-glucanase|Deficiency of exo-1,3-alpha-glucanase|Deficiency of gentiobiase|Deficiency of glucan 1,3-alpha-glucosidase|Deficiency of glucan 1,3-alpha-glucosidase (disorder)|Deficiency of glucokinase|Deficiency of glucokinase (disorder)|Deficiency of gluconate 2-dehydrogenase|Deficiency of gluconate 2-dehydrogenase (disorder)|Deficiency of gluconokinase|Deficiency of gluconokinase (disorder)|Deficiency of gluconolactonase|Deficiency of gluconolactonase (disorder)|Deficiency of glucosamine-6-phosphate isomerase|Deficiency of glucosamine-6-phosphate isomerase (disorder)|Deficiency of glucose dehydrogenase|Deficiency of glucose dehydrogenase (disorder)|Deficiency of glucose oxidase|Deficiency of glucose oxidase (disorder)|Deficiency of glucose oxyhydrase|Deficiency of glucose-1-phosphatase|Deficiency of glucose-1-phosphatase (disorder)|Deficiency of glucose-6-phosphate isomerase|Deficiency of glucose-6-phosphate isomerase (disorder)|Deficiency of glucose-phosphate kinase|Deficiency of glucosulfatase|Deficiency of glucosulphatase|Deficiency of glucosyltransferase 1|Deficiency of glucosyltransferase 1 (disorder)|Deficiency of glyceraldehyde-3-phosphate dehydrogenase|Deficiency of glyceraldehyde-3-phosphate dehydrogenase (disorder)|Deficiency of glycerate phosphomutase|Deficiency of glycerol kinase|Deficiency of glycerol kinase (disorder)|Deficiency of glycogenase|Deficiency of glycosidase|Deficiency of glycosidase (disorder)|Deficiency of glycosulfatase|Deficiency of glycosulfatase (disorder)|Deficiency of glycosulphatase|Deficiency of glycosyltransferase|Deficiency of glycosyltransferase (disorder)|Deficiency of hexosephosphate isomerase|Deficiency of invertase|Deficiency of laminarinase|Deficiency of maltose phosphorylase|Deficiency of maltose phosphorylase (disorder)|Deficiency of mannokinase|Deficiency of mannokinase (disorder)|Deficiency of mutarotase|Deficiency of oxoisomerase|Deficiency of phosphoglucoisomerase|Deficiency of phosphoglucokinase|Deficiency of phosphoglucokinase (disorder)|Deficiency of phosphoglycerate kinase|Deficiency of phosphoglycerate kinase (disorder)|Deficiency of phosphohexose isomerase|Deficiency of phosphomannomutase 2|Deficiency of phosphomannomutase 2 (disorder)|Deficiency of phosphorylase b kinase|Deficiency of phosphorylase b kinase (disorder)|Deficiency of polyol dehydrogenase (NADP^+^)|Deficiency of rhamnulokinase|Deficiency of rhamnulokinase (disorder)|Deficiency of saccharase|Deficiency of saccharogen amylase|Deficiency of transglycosylase|Deficiency of triosephosphate dehydrogenase|Deficiency of xylulokinase|Deficiency of xylulokinase (disorder)|Disacchariduria|Disacchariduria (disorder)|Disorder of glucose metabolism|Disorder of glucose metabolism (disorder)|Disorder of glucose regulation|Disorder of glucose regulation (disorder)|Disorder of glycerate metabolism|Disorder of glycerate metabolism (disorder)|Disorder of glycerol metabolism|Disorder of glycerol metabolism (disorder)|Essential benign pentosuria|Essential pentosuria|Essential pentosuria (disorder)|Familial hyperglycerolaemia|Familial hyperglycerolemia|Familial renal glucosuria|Familial renal glucosuria (disorder)|GK1 deficiency|GKD - Glycerol kinase deficiency|GTT = renal glycosuria|Glucose tolerance test = renal glycosuria|Glucose tolerance test = renal glycosuria (finding)|Glycerol intolerance|Glycerol intolerance (disorder)|Glycerol kinase deficiency|Glycerol kinase deficiency - contiguous gene syndrome|Glycerol kinase deficiency - contiguous gene syndrome (disorder)|Glycerol kinase deficiency - isolated|Glycerol kinase deficiency - isolated (disorder)|Hyperglycerolaemia|Hyperglycerolemia|L-xylulose reductase deficiency|L-xylulosuria|Low renal threshold for glucose|Low renal threshold for glucose (disorder)|Muscle phosphoglycerate mutase deficiency|Muscle phosphoglycerate mutase deficiency (disorder)|Non glucose melituria|Nonglucosuric melituria|Nonglucosuric melituria (disorder)|Pentose disorder|Pentose disorder (disorder)|Phosphoglucomutase deficiency|Renal diabetes|Renal diabetes (disorder)|Renal glucosuria|Renal glucosuria, type A|Renal glucosuria, type A (disorder)|Renal glucosuria, type B|Renal glucosuria, type B (disorder)|Renal glucosuria, type O|Renal glucosuria, type O (disorder)|Renal glycosuria|Renal glycosuria (disorder)|Trehalase deficiency|Trehalose intolerance|Xylitol dehydrogenase deficiency|Xylosuria|Xylosuria (disorder)|alpha, alpha-Trehalase deficiency|alpha, alpha-Trehalase deficiency (disorder)

    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.E74.8 Other specified disorders of carbohydrate metabolism and Essential pentosuria (disorder)

    Essential pentosuria (disorder)
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