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Ehlers Danlos syndrome with a likely monogenic cause v2.8 ATP6V0A2 Ivone Leong Phenotypes for gene: ATP6V0A2 were changed from Cutis laxa, autosomal recessive, type IIA, 219200; Wrinkly skin syndrome, 278250 to Cutis laxa, autosomal recessive, type IIA, OMIM:219200; Wrinkly skin syndrome, OMIM:278250
Ehlers Danlos syndrome with a likely monogenic cause v1.43 ATP6V0A2 Duncan Baker reviewed gene: ATP6V0A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.42 ATP6V0A2 Eleanor Williams reviewed gene: ATP6V0A2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.41 ATP6V0A2 Eleanor Williams Source NHS GMS was added to ATP6V0A2.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Ehlers Danlos syndrome with a likely monogenic cause ATP6V0A2 Angela Brady reviewed ATP6V0A2
Ehlers Danlos syndrome with a likely monogenic cause ATP6V0A2 Neeti Ghali reviewed ATP6V0A2
Ehlers Danlos syndrome with a likely monogenic cause ATP6V0A2 Louise Daugherty classified ATP6V0A2 as green
Ehlers Danlos syndrome with a likely monogenic cause ATP6V0A2 Louise Daugherty reviewed ATP6V0A2