MeSH Browser

MeSH Supplementary: Glycogen Storage Disease, Type IXD
Unique ID: C564485
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564485
Entry Term(s): GSD IXD; GSD9D; Muscle Glycogenosis, X-Linked; Muscle Phosphorylase Kinase Deficiency
Registry Numbers: 0
Heading Mapped to: *Glycogen Storage Disease; *Genetic Diseases, X-Linked
Frequency: 5
Note: mutation in PHKA1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Concept UI: M0564785
Registry Numbers: 0
Terms: Glycogen Storage Disease, Type IXD Preferred Term
Term UI T824300
Date06/20/2012
LexicalTag NON
ThesaurusID OMIM (2013); GSD IXD
Term UI T824299
Date06/20/2012
LexicalTag NON
ThesaurusID OMIM (2013); GSD9D
Term UI T824298
Date06/20/2012
LexicalTag NON
ThesaurusID OMIM (2013); Muscle Glycogenosis, X-Linked
Term UI T804973
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Muscle Phosphorylase Kinase Deficiency
Term UI T804974
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Glycogen Storage Disease, Type IXD MeSH Supplementary Concept Data 2025