E75.22 Glucosylceramidase deficiency

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Glucosylceramidase deficiency

Glucosylceramidase deficiency
Synonym for Gaucher disease

    E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E75 Disorders of sphingolipid metabolism and other lipid storage disorders|E75.2 Other sphingolipidosis

Results for Glucosylceramidase deficiency and additional synonyms


E75.22
Gaucher disease

Synonyms:

Acute cerebral Gaucher's disease|Acute neuronopathic Gaucher disease|Acute neuronopathic Gaucher's disease|Acute neuronopathic Gaucher's disease (disorder)|Adult Gaucher disease|Cerebral acute Gaucher disease|Cerebral degeneration in Gaucher disease|Cerebral degeneration in Gaucher's disease|Cerebral degeneration in Gaucher's disease (disorder)|Cerebroside lipidosis syndrome|Chronic adult Gaucher's disease|Chronic non-neuropathic Gaucher disease|Chronic non-neuropathic Gaucher's disease|Chronic non-neuropathic Gaucher's disease (disorder)|Gaucher splenomegaly|Gaucher syndrome|Gaucher's disease|Gaucher's disease, type I|Gaucher's disease, type II|Gaucher's disease, type III|Glucocerebrosidase deficiency|Glucocerebrosidase deficiency type I|Glucocerebrosidase deficiency type II|Glucocerebrosidase deficiency type III|Glucocerebrosidosis|Glucosylceramidase deficiency|Glucosylceramidase deficiency, acute type|Glucosylceramidase deficiency, chronic type|Glucosylceramidase deficiency, subacute type|Glucosylceramide beta-glucosidase deficiency|Glucosylceramide beta-glucosidase deficiency (disorder)|Infantile Gaucher disease|Infantile Gaucher's disease|Infantile cerebral Gaucher's disease|Juvenile Gaucher disease|Juvenile Gaucher's disease|Kerasin histiocytosis|Kerasin lipoidosis|Kerasin thesaurismosis|Kerasin thesaurismosis (disorder)|Noncerebral juvenile Gaucher's disease|Norrbottnian Gaucher disease|Subacute neuronopathic Gaucher disease|Subacute neuronopathic Gaucher's disease|Subacute neuronopathic Gaucher's disease (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: Glucosylceramidase deficiency

    ICD Code for Disease, Diagnosis E75.22

    ICD Code an Classification Gaucher 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)|E75 Disorders of sphingolipid metabolism and other lipid storage disorders|E75.2 Other sphingolipidosis

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: E75.22: Glucosylceramidase deficiency

    Other Synonyms of the Category: Acute cerebral Gaucher's disease|Acute neuronopathic Gaucher disease|Acute neuronopathic Gaucher's disease|Acute neuronopathic Gaucher's disease (disorder)|Adult Gaucher disease|Cerebral acute Gaucher disease|Cerebral degeneration in Gaucher disease|Cerebral degeneration in Gaucher's disease|Cerebral degeneration in Gaucher's disease (disorder)|Cerebroside lipidosis syndrome|Chronic adult Gaucher's disease|Chronic non-neuropathic Gaucher disease|Chronic non-neuropathic Gaucher's disease|Chronic non-neuropathic Gaucher's disease (disorder)|Gaucher splenomegaly|Gaucher syndrome|Gaucher's disease|Gaucher's disease, type I|Gaucher's disease, type II|Gaucher's disease, type III|Glucocerebrosidase deficiency|Glucocerebrosidase deficiency type I|Glucocerebrosidase deficiency type II|Glucocerebrosidase deficiency type III|Glucocerebrosidosis|Glucosylceramidase deficiency|Glucosylceramidase deficiency, acute type|Glucosylceramidase deficiency, chronic type|Glucosylceramidase deficiency, subacute type|Glucosylceramide beta-glucosidase deficiency|Glucosylceramide beta-glucosidase deficiency (disorder)|Infantile Gaucher disease|Infantile Gaucher's disease|Infantile cerebral Gaucher's disease|Juvenile Gaucher disease|Juvenile Gaucher's disease|Kerasin histiocytosis|Kerasin lipoidosis|Kerasin thesaurismosis|Kerasin thesaurismosis (disorder)|Noncerebral juvenile Gaucher's disease|Norrbottnian Gaucher disease|Subacute neuronopathic Gaucher disease|Subacute neuronopathic Gaucher's disease|Subacute neuronopathic Gaucher's disease (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.E75.22 Gaucher disease and Glucosylceramidase deficiency

    Glucosylceramidase deficiency
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