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Hypertrophic cardiomyopathy v1.53 | MYO6 | Rebecca Whittington commented on gene: MYO6: Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy (606346) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hypertrophic cardiomyopathy v1.52 | MYO6 | Rebecca Whittington commented on gene: MYO6: 1 report of HCM with deafness. 15060111 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hypertrophic cardiomyopathy v1.51 | MYO6 | Rebecca Whittington reviewed gene: MYO6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hypertrophic cardiomyopathy v1.45 | MYO6 |
Ellen McDonagh Source South West GLH was added to MYO6. Mode of inheritance for gene MYO6 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |