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Genetic Epilepsy v0.308 HCCS Zornitza Stark Phenotypes for gene: HCCS were changed from Linear skin defects with multiple congenital anomalies 1, 309801 to Linear skin defects with multiple congenital anomalies 1, 309801
Genetic Epilepsy v0.307 HCCS Zornitza Stark Marked gene: HCCS as ready
Genetic Epilepsy v0.307 HCCS Zornitza Stark Gene: hccs has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.307 HCCS Zornitza Stark Phenotypes for gene: HCCS were changed from to Linear skin defects with multiple congenital anomalies 1, 309801
Genetic Epilepsy v0.306 HCCS Zornitza Stark Publications for gene: HCCS were set to
Genetic Epilepsy v0.306 HCCS Zornitza Stark Added comment: Comment on mode of inheritance: XLD
Genetic Epilepsy v0.306 HCCS Zornitza Stark Mode of inheritance for gene: HCCS was changed from Unknown to Other
Genetic Epilepsy v0.304 HCCS Zornitza Stark Classified gene: HCCS as Amber List (moderate evidence)
Genetic Epilepsy v0.304 HCCS Zornitza Stark Gene: hccs has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.303 HCCS Zornitza Stark reviewed gene: HCCS: Rating: AMBER; Mode of pathogenicity: None; Publications: 17033964; Phenotypes: Linear skin defects with multiple congenital anomalies 1, 309801; Mode of inheritance: Other
Genetic Epilepsy v0.0 HCCS Zornitza Stark gene: HCCS was added
gene: HCCS was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Epilepsy Flagship,Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: HCCS was set to Unknown