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Intellectual disability syndromic and non-syndromic v0.170 EPM2A Zornitza Stark Marked gene: EPM2A as ready
Intellectual disability syndromic and non-syndromic v0.170 EPM2A Zornitza Stark Gene: epm2a has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.170 EPM2A Zornitza Stark Phenotypes for gene: EPM2A were changed from to Epilepsy, progressive myoclonic 2A (Lafora), MIM#254780
Intellectual disability syndromic and non-syndromic v0.169 EPM2A Zornitza Stark Mode of inheritance for gene: EPM2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.168 EPM2A Zornitza Stark Classified gene: EPM2A as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.168 EPM2A Zornitza Stark Gene: epm2a has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.167 EPM2A Zornitza Stark edited their review of gene: EPM2A: Changed rating: RED
Intellectual disability syndromic and non-syndromic v0.167 EPM2A Zornitza Stark reviewed gene: EPM2A: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 2A (Lafora), MIM#254780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.0 EPM2A Zornitza Stark gene: EPM2A was added
gene: EPM2A was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland
Mode of inheritance for gene: EPM2A was set to Unknown