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Severe Paediatric Disorders v0.12 WDR19 Louise Daugherty reviewed gene: WDR19: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 WDR19 Louise Daugherty Publications for gene WDR19 were updated from to 30847515
Severe Paediatric Disorders v0.10 WDR19 Louise Daugherty Added phenotypes Senior-Loken syndrome 8, 616307; ?Cranioectodermal dysplasia 4, 614378; Nephronophthisis 13, 614377; ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376 for gene: WDR19
Severe Paediatric Disorders v0.9 WDR19 Louise Daugherty Added phenotypes Senior-Loken syndrome 8, 616307; ?Cranioectodermal dysplasia 4, 614378; Nephronophthisis 13, 614377; ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376 for gene: WDR19
Severe Paediatric Disorders v0.9 WDR19 Louise Daugherty Added phenotypes Senior-Loken syndrome 8, 616307; ?Cranioectodermal dysplasia 4, 614378; Nephronophthisis 13, 614377; ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376 for gene: WDR19
Severe Paediatric Disorders v0.8 WDR19 Louise Daugherty Added phenotypes ?Cranioectodermal dysplasia 4, 614378; ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376; Senior-Loken syndrome 8, 616307; Nephronophthisis 13, 614377 for gene: WDR19
Severe Paediatric Disorders v0.8 WDR19 Louise Daugherty Mode of inheritance for gene WDR19 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Senior-Loken syndrome 8, 616307; ?Cranioectodermal dysplasia 4, 614378; Nephronophthisis 13, 614377; ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376 for gene: WDR19
Severe Paediatric Disorders v0.7 WDR19 Louise Daugherty Source Next Generation Children Project was added to WDR19.
Severe Paediatric Disorders v0.5 WDR19 Louise Daugherty Source Expert Review Green was added to WDR19.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 WDR19 Louise Daugherty gene: WDR19 was added
gene: WDR19 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: WDR19 was set to