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Familial Neural Tube Defects v1.7 B9D2 Arina Puzriakova Phenotypes for gene: B9D2 were changed from Meckel Syndrome to Joubert syndrome 34, OMIM:614175; Meckel syndrome 10, OMIM:614175; Meckel syndrome, type 10, MONDO:0013609
Familial Neural Tube Defects B9D2 Ellen McDonagh classified B9D2 as red