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Severe Paediatric Disorders v0.17 CLDN19 Louise Daugherty Mode of inheritance for gene CLDN19 was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.12 CLDN19 Louise Daugherty reviewed gene: CLDN19: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 CLDN19 Louise Daugherty Publications for gene CLDN19 were updated from to 30847515
Severe Paediatric Disorders v0.10 CLDN19 Louise Daugherty Added phenotypes Hypomagnesemia 5, renal, with ocular involvement, 248190 for gene: CLDN19
Severe Paediatric Disorders v0.9 CLDN19 Louise Daugherty Added phenotypes Hypomagnesemia 5, renal, with ocular involvement, 248190 for gene: CLDN19
Severe Paediatric Disorders v0.9 CLDN19 Louise Daugherty Added phenotypes Hypomagnesemia 5, renal, with ocular involvement, 248190 for gene: CLDN19
Severe Paediatric Disorders v0.8 CLDN19 Louise Daugherty Added phenotypes Hypomagnesemia 5, renal, with ocular involvement, 248190 for gene: CLDN19
Severe Paediatric Disorders v0.7 CLDN19 Louise Daugherty Source Next Generation Children Project was added to CLDN19.
Severe Paediatric Disorders v0.5 CLDN19 Louise Daugherty Source Expert Review Green was added to CLDN19.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 CLDN19 Louise Daugherty gene: CLDN19 was added
gene: CLDN19 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: CLDN19 was set to