E75.25 van Bogaert-Nijssen disease

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van Bogaert-Nijssen disease

van Bogaert-Nijssen disease
Synonym for Metachromatic leukodystrophy

    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 van Bogaert-Nijssen disease and additional synonyms


E75.25
Metachromatic leukodystrophy

Synonyms:

ARSA - Arylsulfatase A deficiency|ARSA - Arylsulphatase A deficiency|Adult metachromatic leucodystrophy|Adult metachromatic leukodystrophy|Arylsulfatase A deficiency|Arylsulfatase A deficiency (disorder)|Arylsulphatase A deficiency|Cerebroside sulfatase deficiency|Cerebroside sulphatase deficiency|Familial progressive cerebral sclerosis|Greenfield disease|Juvenile metachromatic leucodystrophy|Late infantile metachromatic leucodystrophy|MLD|MLD - Metachromatic leucodystrophy|Metachromatic leucodystrophy|Metachromatic leucodystrophy (disorder)|Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator|Metachromatic leucodystrophy without arylsulphatase deficiency|Metachromatic leucodystrophy, adult type|Metachromatic leucodystrophy, congenital type|Metachromatic leucodystrophy, juvenile type|Metachromatic leucodystrophy, late infantile type|Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator|Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)|Metachromatic leukodystrophy without arylsulfatase deficiency|Metachromatic leukodystrophy without arylsulfatase deficiency (disorder)|Metachromatic leukodystrophy, adult type|Metachromatic leukodystrophy, adult type (disorder)|Metachromatic leukodystrophy, congenital type|Metachromatic leukodystrophy, congenital type (disorder)|Metachromatic leukodystrophy, juvenile type|Metachromatic leukodystrophy, juvenile type (disorder)|Metachromatic leukodystrophy, late infantile type|Metachromatic leukodystrophy, late infantile type (disorder)|Metachromatic leukoencephaly|SAPI - Sphingolipid activator protein I deficiency|Saposin B deficiency|Scholz cerebral sclerosis|Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis|Severe deficiency of arylsulfatase|Severe deficiency of arylsulphatase|Sphingolipid activator protein 1 deficiency|Sphingolipid activator protein 1 deficiency (disorder)|Sulfatide lipidosis|Sulphatide lipidosis|van Bogaert-Nijssen 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: van Bogaert-Nijssen disease

    ICD Code for Disease, Diagnosis E75.25

    ICD Code an Classification Metachromatic leukodystrophy

    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: E75.25: van Bogaert-Nijssen disease

    Other Synonyms of the Category: ARSA - Arylsulfatase A deficiency|ARSA - Arylsulphatase A deficiency|Adult metachromatic leucodystrophy|Adult metachromatic leukodystrophy|Arylsulfatase A deficiency|Arylsulfatase A deficiency (disorder)|Arylsulphatase A deficiency|Cerebroside sulfatase deficiency|Cerebroside sulphatase deficiency|Familial progressive cerebral sclerosis|Greenfield disease|Juvenile metachromatic leucodystrophy|Late infantile metachromatic leucodystrophy|MLD|MLD - Metachromatic leucodystrophy|Metachromatic leucodystrophy|Metachromatic leucodystrophy (disorder)|Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator|Metachromatic leucodystrophy without arylsulphatase deficiency|Metachromatic leucodystrophy, adult type|Metachromatic leucodystrophy, congenital type|Metachromatic leucodystrophy, juvenile type|Metachromatic leucodystrophy, late infantile type|Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator|Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)|Metachromatic leukodystrophy without arylsulfatase deficiency|Metachromatic leukodystrophy without arylsulfatase deficiency (disorder)|Metachromatic leukodystrophy, adult type|Metachromatic leukodystrophy, adult type (disorder)|Metachromatic leukodystrophy, congenital type|Metachromatic leukodystrophy, congenital type (disorder)|Metachromatic leukodystrophy, juvenile type|Metachromatic leukodystrophy, juvenile type (disorder)|Metachromatic leukodystrophy, late infantile type|Metachromatic leukodystrophy, late infantile type (disorder)|Metachromatic leukoencephaly|SAPI - Sphingolipid activator protein I deficiency|Saposin B deficiency|Scholz cerebral sclerosis|Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis|Severe deficiency of arylsulfatase|Severe deficiency of arylsulphatase|Sphingolipid activator protein 1 deficiency|Sphingolipid activator protein 1 deficiency (disorder)|Sulfatide lipidosis|Sulphatide lipidosis|van Bogaert-Nijssen 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.E75.25 Metachromatic leukodystrophy and van Bogaert-Nijssen disease

    van Bogaert-Nijssen disease
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