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Structural basal ganglia disorders v1.39 KMT2B Arina Puzriakova Phenotypes for gene: KMT2B were changed from Dystonia 28, childhood-onset 617284 to Dystonia 28, childhood-onset, OMIM:617284; early-onset dystonia
Structural basal ganglia disorders KMT2B Sarah Leigh marked KMT2B as ready
Structural basal ganglia disorders KMT2B Sarah Leigh classified KMT2B as green
Structural basal ganglia disorders KMT2B Sarah Leigh commented on KMT2B
Structural basal ganglia disorders KMT2B Manju Kurian added KMT2B to panel
Structural basal ganglia disorders KMT2B Manju Kurian reviewed KMT2B