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Glycogen storage disease V v1.3 PYGM Achchuthan Shanmugasundram Phenotypes for gene: PYGM were changed from Glycogen storage disease V, OMIM:232600; glycogen storage disease V, MONDO:0009293 to McArdle disease, OMIM:232600; glycogen storage disease V, MONDO:0009293
Glycogen storage disease V v1.2 PYGM Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #232600) and the OMIM record was last accessed on 18 December 2025.
Glycogen storage disease V v1.2 PYGM Achchuthan Shanmugasundram Phenotypes for gene: PYGM were changed from to Glycogen storage disease V, OMIM:232600; glycogen storage disease V, MONDO:0009293
Glycogen storage disease V v0.1 PYGM Achchuthan Shanmugasundram reviewed gene: PYGM: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Glycogen storage disease V v0.1 PYGM Achchuthan Shanmugasundram gene: PYGM was added
gene: PYGM was added to Glycogen storage disease V. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: PYGM was set to BIALLELIC, autosomal or pseudoautosomal