MYH6

myosin heavy chain 6
OMIM: 160710
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
ATRIAL SEPTAL DEFECT TYPE 3, CARDIOMYOPATHY DILATED TYPE 1EE, CARDIOMYOPATHY FAMILIAL HYPERTROPHIC TYPE 14
Component of the following Super Panels:
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R135
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Atrial septal defect 3, OMIM:614089, Cardiomyopathy, dilated, 1EE OMIM:613252, Cardiomyopathy, hypertrophic, 14, OMIM:613251, {Sick sinus syndrome 3}, OMIM:614090