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Ehlers Danlos syndrome with a likely monogenic cause v2.7 ALDH18A1 Ivone Leong Phenotypes for gene: ALDH18A1 were changed from Cutis laxa, autosomal recessive, type IIIA, 219150; Cutis laxa, autosomal dominant 3, 616603 to Cutis laxa, autosomal recessive, type IIIA, OMIM:219150; Cutis laxa, autosomal dominant 3, OMIM:616603
Ehlers Danlos syndrome with a likely monogenic cause v1.43 ALDH18A1 Duncan Baker reviewed gene: ALDH18A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.42 ALDH18A1 Eleanor Williams reviewed gene: ALDH18A1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.41 ALDH18A1 Eleanor Williams Source NHS GMS was added to ALDH18A1.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Ehlers Danlos syndrome with a likely monogenic cause ALDH18A1 Angela Brady reviewed ALDH18A1
Ehlers Danlos syndrome with a likely monogenic cause ALDH18A1 Neeti Ghali reviewed ALDH18A1
Ehlers Danlos syndrome with a likely monogenic cause ALDH18A1 Louise Daugherty edited their review of ALDH18A1
Ehlers Danlos syndrome with a likely monogenic cause ALDH18A1 Louise Daugherty classified ALDH18A1 as green
Ehlers Danlos syndrome with a likely monogenic cause ALDH18A1 Louise Daugherty commented on ALDH18A1