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Rhabdomyolysis and metabolic muscle disorders v3.2 SUCLA2 Arina Puzriakova Phenotypes for gene: SUCLA2 were changed from Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) 612073 to Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria), OMIM:612073
Rhabdomyolysis and metabolic muscle disorders v1.24 TK2 Louise Daugherty Added comment: Comment on phenotypes: changed phenotype to Mitochondrial DNA depletion syndrome 2 (myopathic type), as Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) 612073 relates to variants of the gene SUCLA2, not TK2
Rhabdomyolysis and metabolic muscle disorders SUCLA2 Sarah Leigh marked SUCLA2 as ready
Rhabdomyolysis and metabolic muscle disorders SUCLA2 Sarah Leigh added SUCLA2 to panel
Rhabdomyolysis and metabolic muscle disorders SUCLA2 Sarah Leigh reviewed SUCLA2