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Deafness and congenital structural abnormalities v1.27 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from Bilateral Microtia; 224690; Meier Gorlin EPS; causes microtia and syndromic features; Meier-Gorlin syndrome 1 to Meier-Gorlin syndrome 1, OMIM:224690; Bilateral Microtia
Deafness and congenital structural abnormalities ORC1 Ellen McDonagh marked ORC1 as ready