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Congenital myopathy v3.61 MEGF10 Arina Puzriakova Phenotypes for gene: MEGF10 were changed from Myopathy, Early-Onset, Areflexia, Respiratory Distress, andDysphagia; Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, 614399 to Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, OMIM:614399; Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant, OMIM:614399
Congenital myopathy v1.120 MEGF10 Rachael Mein edited their review of gene: MEGF10: Changed publications: 22101682; Changed phenotypes: Myopathy, Early-Onset, Areflexia, Respiratory Distress, andDysphagia, Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, 614399
Congenital myopathy v1.76 MEGF10 Louise Daugherty reviewed gene: MEGF10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Congenital myopathy v1.75 MEGF10 Rachael Mein reviewed gene: MEGF10: Rating: GREEN; Mode of pathogenicity: ; Publications: 12084876, 21415759; Phenotypes: vacuolar myopathy?; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Congenital myopathy v1.74 MEGF10 Louise Daugherty Source NHS GMS was added to MEGF10.
Congenital myopathy v1.73 MEGF10 Louise Daugherty Source London South GLH was added to MEGF10.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Congenital myopathy MEGF10 Anna Sarkozy reviewed MEGF10
Congenital myopathy MEGF10 Helen Brittain marked MEGF10 as ready
Congenital myopathy MEGF10 Helen Brittain classified MEGF10 as green
Congenital myopathy MEGF10 Helen Brittain reviewed MEGF10