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Congenital ophthalmoplegia v0.64 MYH2 Zornitza Stark Marked gene: MYH2 as ready
Congenital ophthalmoplegia v0.64 MYH2 Zornitza Stark Gene: myh2 has been classified as Green List (High Evidence).
Congenital ophthalmoplegia v0.64 MYH2 Zornitza Stark Phenotypes for gene: MYH2 were changed from to Proximal myopathy and ophthalmoplegia, MIM# 605637
Congenital ophthalmoplegia v0.63 MYH2 Zornitza Stark Classified gene: MYH2 as Green List (high evidence)
Congenital ophthalmoplegia v0.63 MYH2 Zornitza Stark Gene: myh2 has been classified as Green List (High Evidence).
Congenital ophthalmoplegia v0.62 MYH2 Zornitza Stark reviewed gene: MYH2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Proximal myopathy and ophthalmoplegia, MIM# 605637; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital ophthalmoplegia v0.59 MYH2 Shannon LeBlanc gene: MYH2 was added
gene: MYH2 was added to Congenital ophthalmoplegia. Sources: Literature
Mode of inheritance for gene: MYH2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: MYH2 were set to PMID 24193343; 32578970; 11114175; 23489661
Added comment: childhood consent ophthalmoplegia and progressive proximal limb weakness. Either slowly progressive or non-progressive.

> 10 families reported with balletic variants
monoallelic variants: two missense variants reported
Sources: Literature