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Ehlers Danlos syndrome with a likely monogenic cause v2.28 EFEMP2 Ivone Leong Phenotypes for gene: EFEMP2 were changed from Cutis laxa, autosomal recessive, type IB, 614437 to Cutis laxa, autosomal recessive, type IB, OMIM:614437
Ehlers Danlos syndrome with a likely monogenic cause v1.43 EFEMP2 Duncan Baker reviewed gene: EFEMP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.42 EFEMP2 Eleanor Williams reviewed gene: EFEMP2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.41 EFEMP2 Eleanor Williams Source NHS GMS was added to EFEMP2.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Ehlers Danlos syndrome with a likely monogenic cause EFEMP2 Angela Brady reviewed EFEMP2
Ehlers Danlos syndrome with a likely monogenic cause EFEMP2 Neeti Ghali reviewed EFEMP2
Ehlers Danlos syndrome with a likely monogenic cause EFEMP2 Louise Daugherty classified EFEMP2 as green
Ehlers Danlos syndrome with a likely monogenic cause EFEMP2 Louise Daugherty reviewed EFEMP2