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Ehlers Danlos syndrome with a likely monogenic cause v2.53 ACTA2 Ivone Leong Added comment: Comment on phenotypes: Previous phenotypes:
Thoracic aortic aneurysm and dissection;Aortic aneurysm, familial thoracic 6;611788;Moyamoya disease 5;614042;Thoracic aneurysms congenital mydriasis;moya moya syndrome
Ehlers Danlos syndrome with a likely monogenic cause v2.53 ACTA2 Ivone Leong Phenotypes for gene: ACTA2 were changed from Thoracic aortic aneurysm and dissection; Aortic aneurysm, familial thoracic 6; 611788; Moyamoya disease 5; 614042; Thoracic aneurysms congenital mydriasis; moya moya syndrome to Aortic aneurysm, familial thoracic 6, OMIM:611788
Ehlers Danlos syndrome with a likely monogenic cause v1.63 ACTA2 Eleanor Williams Mode of inheritance for gene: ACTA2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Ehlers Danlos syndrome with a likely monogenic cause ACTA2 Helen Brittain commented on ACTA2
Ehlers Danlos syndrome with a likely monogenic cause ACTA2 Louise Daugherty classified ACTA2 as amber
Ehlers Danlos syndrome with a likely monogenic cause ACTA2 Louise Daugherty classified ACTA2 as green
Ehlers Danlos syndrome with a likely monogenic cause ACTA2 Louise Daugherty commented on ACTA2
Ehlers Danlos syndrome with a likely monogenic cause ACTA2 Angela Brady reviewed ACTA2
Ehlers Danlos syndrome with a likely monogenic cause ACTA2 Neeti Ghali reviewed ACTA2