Glycogen Storage Disease, Type IXA2 MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Glycogen Storage Disease, Type IXA2
Unique ID: C567579
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567579
Entry Term(s): GSD IXA2; GSD9A2
Registry Numbers: 0
Heading Mapped to: *Glycogen Storage Disease; *Genetic Diseases, X-Linked
Frequency: 2
Note: PROM mutation in PHKA2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Glycogen Storage Disease, Type IXA2 Preferred

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