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Glycogen Storage Disease Type IIb MeSH Descriptor Data 2023


MeSH Heading
Glycogen Storage Disease Type IIb
Tree Number(s)
C10.597.606.360.455.562
C14.280.238.458
C16.320.322.201
C16.320.565.202.449.510
C18.452.648.202.449.510
Unique ID
D052120
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D052120
Scope Note
An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2.
Entry Term(s)
Antopol Disease
Danon Disease
Glycogen Storage Cardiomyopathy
Glycogen Storage Disease IIb
Glycogen Storage Disease Limited to the Heart
Glycogen Storage Disease Type 2B
Lysosomal Glycogen Storage Disease with Normal Acid Maltase
Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency
Pseudoglycogenosis 2
Pseudoglycogenosis II
Vacuolar Cardiomyopathy and Myopathy, X-linked
X-Linked Vacuolar Cardiomyopathy and Myopathy
Public MeSH Note
2006
History Note
2006
Date Established
2006/01/01
Date of Entry
2005/06/30
Revision Date
2018/06/30
Glycogen Storage Disease Type IIb Preferred
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