Lysosomal Storage Diseases, Nervous System D020140

Related MeSH Hierarchy (6)

Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Brain Diseases » Brain Diseases, Metabolic » Brain Diseases, Metabolic, Inborn » Lysosomal Storage Diseases, Nervous System

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Brain Diseases, Metabolic » Brain Diseases, Metabolic, Inborn » Lysosomal Storage Diseases, Nervous System

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Brain Diseases, Metabolic, Inborn » Lysosomal Storage Diseases, Nervous System

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Lysosomal Storage Diseases » Lysosomal Storage Diseases, Nervous System

Description

A group of enzymatic disorders affecting the nervous system and to a variable degree the skeletal system, lymphoreticular system, and other organs. The conditions are marked by an abnormal accumulation of catabolic material within lysosomes.   MeSH

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Subtype Terms (5)

Fucosidosis
11 drugs (8 approved, 3 experimental)

Glycogen Storage Disease Type II
28 drugs (15 approved, 13 experimental)

Mucolipidoses
7 drugs (6 approved, 1 experimental)

Sialic Acid Storage Disease
 

Sphingolipidoses
9 drugs (7 approved, 2 experimental)

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UMLS Data


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