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Severe Paediatric Disorders v0.17 CFHR5 Louise Daugherty Mode of inheritance for gene CFHR5 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 CFHR5 Louise Daugherty reviewed gene: CFHR5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 CFHR5 Louise Daugherty Publications for gene CFHR5 were updated from to 30847515
Severe Paediatric Disorders v0.10 CFHR5 Louise Daugherty Added phenotypes Nephropathy due to CFHR5 deficiency, 614809 for gene: CFHR5
Severe Paediatric Disorders v0.9 CFHR5 Louise Daugherty Added phenotypes Nephropathy due to CFHR5 deficiency, 614809 for gene: CFHR5
Severe Paediatric Disorders v0.9 CFHR5 Louise Daugherty Added phenotypes Nephropathy due to CFHR5 deficiency, 614809 for gene: CFHR5
Severe Paediatric Disorders v0.8 CFHR5 Louise Daugherty Added phenotypes Nephropathy due to CFHR5 deficiency, 614809 for gene: CFHR5
Severe Paediatric Disorders v0.7 CFHR5 Louise Daugherty Source Next Generation Children Project was added to CFHR5.
Severe Paediatric Disorders v0.5 CFHR5 Louise Daugherty Source Expert Review Green was added to CFHR5.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 CFHR5 Louise Daugherty gene: CFHR5 was added
gene: CFHR5 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: CFHR5 was set to