E74.09 Glycogen storage disease type VIII

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Glycogen storage disease type VIII

Glycogen storage disease type VIII
Synonym for Other glycogen storage disease

    E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E74 Other disorders of carbohydrate metabolism|E74.0 Glycogen storage disease

Results for Glycogen storage disease type VIII and additional synonyms


E74.09
Other glycogen storage disease

Synonyms:

1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency|Amylopectinosis|Andersen disease|Andersen's disease|Brancher deficiency glycogen storage disease|Branching enzyme deficiency|Branching-transferase deficiency glycogenosis|Cardiac glycogen phosphorylase kinase deficiency|Cardiac glycogen phosphorylase kinase deficiency (disorder)|Danon disease|Danon disease (disorder)|Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase|Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase (disorder)|Deficiency of alpha-galactosidase|Deficiency of alpha-galactosidase (disorder)|Deficiency of melibiase|Fanconi-Bickel syndrome|GSD IV|GSD VI|GSD VII|GSD VIII|GSD X|Glycogen phosphorylase kinase deficiency|Glycogen phosphorylase kinase deficiency (disorder)|Glycogen phosphorylase kinase deficiency, X-linked|Glycogen phosphorylase kinase deficiency, X-linked (disorder)|Glycogen phosphorylase kinase deficiency, autosomal recessive|Glycogen phosphorylase kinase deficiency, autosomal recessive (disorder)|Glycogen storage disease VIII|Glycogen storage disease type 0|Glycogen storage disease type 8|Glycogen storage disease type 9|Glycogen storage disease type IV|Glycogen storage disease type IX|Glycogen storage disease type Ic|Glycogen storage disease type VIII|Glycogen storage disease type VIII (disorder)|Glycogen storage disease type X|Glycogen storage disease type X (disorder)|Glycogen storage disease, hepatic form|Glycogen storage disease, hepatic form (disorder)|Glycogen storage disease, muscular form|Glycogen storage disease, muscular form (disorder)|Glycogen storage disease, type 4|Glycogen storage disease, type 7|Glycogen storage disease, type IV|Glycogen storage disease, type IV (disorder)|Glycogen storage disease, type IX|Glycogen storage disease, type IX (disorder)|Glycogen storage disease, type VI|Glycogen storage disease, type VI (disorder)|Glycogen storage disease, type VII|Glycogen storage disease, type VII (disorder)|Glycogen storage disease, types 0, IV, VI-XI|Glycogen synthase deficiency|Glycogen synthase deficiency (disorder)|Glycogenosis due to inactive hepatic glycogen phosphorylase|Glycogenosis due to inactive phosphorylase|Glycogenosis due to inactive phosphorylase AND kinase|Glycogenosis viiia|Glycogenosis with glucoaminophosphaturia|Glycogenosis with glucoaminophosphaturia (disorder)|Glycogenosis, type 4|Hepatic and muscle glycogen phosphorylase kinase deficiency|Hepatic and muscle glycogen phosphorylase kinase deficiency (disorder)|Hepatic glycogen phosphorylase deficiency|Hepatic glycogen phosphorylase kinase deficiency|Hepatic glycogen phosphorylase kinase deficiency (disorder)|Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome|Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome|Hepatic phosphorylase deficiency|Hepatic phosphorylase kinase deficiency|Hers disease|Liver phosphorylase deficiency|Muscle phosphofructokinase deficiency|PHK - Hepatic phosphorylase kinase deficiency|Phosphate transport defect|Phosphate transport defect (disorder)|Phosphorylase kinase deficiency of liver|Pseudo-phlorizin diabetes|Renal glucose-losing syndrome|Tarui's disease|Tauri disease

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: Glycogen storage disease type VIII

    ICD Code for Disease, Diagnosis E74.09

    ICD Code an Classification Other glycogen storage disease

    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|E74.0 Glycogen storage disease

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: E74.09: Glycogen storage disease type VIII

    Other Synonyms of the Category: 1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency|Amylopectinosis|Andersen disease|Andersen's disease|Brancher deficiency glycogen storage disease|Branching enzyme deficiency|Branching-transferase deficiency glycogenosis|Cardiac glycogen phosphorylase kinase deficiency|Cardiac glycogen phosphorylase kinase deficiency (disorder)|Danon disease|Danon disease (disorder)|Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase|Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase (disorder)|Deficiency of alpha-galactosidase|Deficiency of alpha-galactosidase (disorder)|Deficiency of melibiase|Fanconi-Bickel syndrome|GSD IV|GSD VI|GSD VII|GSD VIII|GSD X|Glycogen phosphorylase kinase deficiency|Glycogen phosphorylase kinase deficiency (disorder)|Glycogen phosphorylase kinase deficiency, X-linked|Glycogen phosphorylase kinase deficiency, X-linked (disorder)|Glycogen phosphorylase kinase deficiency, autosomal recessive|Glycogen phosphorylase kinase deficiency, autosomal recessive (disorder)|Glycogen storage disease VIII|Glycogen storage disease type 0|Glycogen storage disease type 8|Glycogen storage disease type 9|Glycogen storage disease type IV|Glycogen storage disease type IX|Glycogen storage disease type Ic|Glycogen storage disease type VIII|Glycogen storage disease type VIII (disorder)|Glycogen storage disease type X|Glycogen storage disease type X (disorder)|Glycogen storage disease, hepatic form|Glycogen storage disease, hepatic form (disorder)|Glycogen storage disease, muscular form|Glycogen storage disease, muscular form (disorder)|Glycogen storage disease, type 4|Glycogen storage disease, type 7|Glycogen storage disease, type IV|Glycogen storage disease, type IV (disorder)|Glycogen storage disease, type IX|Glycogen storage disease, type IX (disorder)|Glycogen storage disease, type VI|Glycogen storage disease, type VI (disorder)|Glycogen storage disease, type VII|Glycogen storage disease, type VII (disorder)|Glycogen storage disease, types 0, IV, VI-XI|Glycogen synthase deficiency|Glycogen synthase deficiency (disorder)|Glycogenosis due to inactive hepatic glycogen phosphorylase|Glycogenosis due to inactive phosphorylase|Glycogenosis due to inactive phosphorylase AND kinase|Glycogenosis viiia|Glycogenosis with glucoaminophosphaturia|Glycogenosis with glucoaminophosphaturia (disorder)|Glycogenosis, type 4|Hepatic and muscle glycogen phosphorylase kinase deficiency|Hepatic and muscle glycogen phosphorylase kinase deficiency (disorder)|Hepatic glycogen phosphorylase deficiency|Hepatic glycogen phosphorylase kinase deficiency|Hepatic glycogen phosphorylase kinase deficiency (disorder)|Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome|Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome|Hepatic phosphorylase deficiency|Hepatic phosphorylase kinase deficiency|Hers disease|Liver phosphorylase deficiency|Muscle phosphofructokinase deficiency|PHK - Hepatic phosphorylase kinase deficiency|Phosphate transport defect|Phosphate transport defect (disorder)|Phosphorylase kinase deficiency of liver|Pseudo-phlorizin diabetes|Renal glucose-losing syndrome|Tarui's disease|Tauri disease

    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.E74.09 Other glycogen storage disease and Glycogen storage disease type VIII

    Glycogen storage disease type VIII
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