E74.02 Lysosomal alpha-1,4-glucosidase deficiency (disorder)

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Lysosomal alpha-1,4-glucosidase deficiency (disorder)

Lysosomal alpha-1,4-glucosidase deficiency (disorder)
Synonym for Pompe 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 Lysosomal alpha-1,4-glucosidase deficiency (disorder) and additional synonyms


E74.02
Pompe disease

Synonyms:

AMD - Acid maltase deficiency|Acid maltase deficiency|Cardiac glycogenosis|Cardiac glycogenosis (disorder)|Deficiency of acid maltase|Deficiency of alpha-glucosidase|Deficiency of alpha-glucosidase (disorder)|Deficiency of amyloglucosidase|Deficiency of exo-1,4-alpha-glucosidase|Deficiency of gamma-amylase|Deficiency of glucan 1,4-alpha-glucosidase|Deficiency of glucan 1,4-alpha-glucosidase (disorder)|Deficiency of glucoamylase|Deficiency of glucoinvertase|Deficiency of glucosidosucrase|Deficiency of maltase|Fatal congenital nonlysosomal heart glycogenosis|Fatal congenital nonlysosomal heart glycogenosis (disorder)|Generalised glycogen storage disease of infants|Generalized glycogen storage disease of infants|Glycogen heart disease|Glycogen storage disease, type II|Glycogen storage disease, type II (disorder)|Lysosomal alpha-1,4-glucosidase deficiency|Lysosomal alpha-1,4-glucosidase deficiency (disorder)|Lysosomal alpha-1,4-glucosidase deficiency - adult onset|Lysosomal alpha-1,4-glucosidase deficiency - adult onset (disorder)|Lysosomal alpha-1,4-glucosidase deficiency - juvenile onset|Lysosomal alpha-1,4-glucosidase deficiency - juvenile onset (disorder)|Pompe's disease|Type II glycogen storage disease|alpha-1,4-Glucosidase deficiency|alpha-Glucosidase deficiency

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: Lysosomal alpha-1,4-glucosidase deficiency (disorder)

    ICD Code for Disease, Diagnosis E74.02

    ICD Code an Classification Pompe 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: E74.02: Lysosomal alpha-1,4-glucosidase deficiency (disorder)

    Other Synonyms of the Category: AMD - Acid maltase deficiency|Acid maltase deficiency|Cardiac glycogenosis|Cardiac glycogenosis (disorder)|Deficiency of acid maltase|Deficiency of alpha-glucosidase|Deficiency of alpha-glucosidase (disorder)|Deficiency of amyloglucosidase|Deficiency of exo-1,4-alpha-glucosidase|Deficiency of gamma-amylase|Deficiency of glucan 1,4-alpha-glucosidase|Deficiency of glucan 1,4-alpha-glucosidase (disorder)|Deficiency of glucoamylase|Deficiency of glucoinvertase|Deficiency of glucosidosucrase|Deficiency of maltase|Fatal congenital nonlysosomal heart glycogenosis|Fatal congenital nonlysosomal heart glycogenosis (disorder)|Generalised glycogen storage disease of infants|Generalized glycogen storage disease of infants|Glycogen heart disease|Glycogen storage disease, type II|Glycogen storage disease, type II (disorder)|Lysosomal alpha-1,4-glucosidase deficiency|Lysosomal alpha-1,4-glucosidase deficiency (disorder)|Lysosomal alpha-1,4-glucosidase deficiency - adult onset|Lysosomal alpha-1,4-glucosidase deficiency - adult onset (disorder)|Lysosomal alpha-1,4-glucosidase deficiency - juvenile onset|Lysosomal alpha-1,4-glucosidase deficiency - juvenile onset (disorder)|Pompe's disease|Type II glycogen storage disease|alpha-1,4-Glucosidase deficiency|alpha-Glucosidase deficiency

    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.E74.02 Pompe disease and Lysosomal alpha-1,4-glucosidase deficiency (disorder)

    Lysosomal alpha-1,4-glucosidase deficiency (disorder)
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