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Congenital myopathy v3.117 VCP Arina Puzriakova Phenotypes for gene: VCP were changed from Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia 613954; Charcot-Marie-Tooth disease, type 2Y 616687; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1 167320 to Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, OMIM:167320
Congenital myopathy VCP Anna Sarkozy reviewed VCP
Congenital myopathy VCP Helen Brittain marked VCP as ready
Congenital myopathy VCP Helen Brittain classified VCP as red
Congenital myopathy VCP Helen Brittain reviewed VCP