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Ehlers Danlos syndrome with a likely monogenic cause v2.30 FBLN5 Ivone Leong Phenotypes for gene: FBLN5 were changed from Cutis laxa, autosomal dominant 2, 614434; Cutis laxa, autosomal recessive, type IA, 219100 to ?Cutis laxa, autosomal dominant 2, OMIM:614434; Cutis laxa, autosomal recessive, type IA, OMIM:219100
Ehlers Danlos syndrome with a likely monogenic cause v1.43 FBLN5 Duncan Baker reviewed gene: FBLN5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.42 FBLN5 Eleanor Williams reviewed gene: FBLN5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ehlers Danlos syndrome with a likely monogenic cause v1.41 FBLN5 Eleanor Williams Source NHS GMS was added to FBLN5.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Ehlers Danlos syndrome with a likely monogenic cause FBLN5 Angela Brady reviewed FBLN5
Ehlers Danlos syndrome with a likely monogenic cause FBLN5 Neeti Ghali reviewed FBLN5
Ehlers Danlos syndrome with a likely monogenic cause FBLN5 Louise Daugherty classified FBLN5 as green
Ehlers Danlos syndrome with a likely monogenic cause FBLN5 Louise Daugherty commented on FBLN5