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Arthrogryposis v3.92 DPM2 Arina Puzriakova Phenotypes for gene: DPM2 were changed from congenital muscular dystrophies; congenital muscular dystrophies. DPM2-CDG . Musclular dystrophy dystroglycanopathy syndrome with severe epilepsy. to Congenital disorder of glycosylation, type Iu, OMIM:615042
Arthrogryposis DPM2 Alice Gardham marked DPM2 as ready
Arthrogryposis DPM2 Alice Gardham classified DPM2 as amber
Arthrogryposis DPM2 Alice Gardham commented on DPM2