MYH6

myosin heavy chain 6
OMIM: 160710
PanelMode of inheritanceDetails
3 panels
R-numbers: R135
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Cardiomyopathy, dilated, 1EE, Cardiomyopathy, familial hypertrophic, 14
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CARDIOMYOPATHY DILATED TYPE 1EE 613252, CARDIOMYOPATHY FAMILIAL HYPERTROPHIC TYPE 14 613251, ATRIAL SEPTAL DEFECT TYPE 3 614089
R-numbers: R21
Signed-off version 1.92
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ATRIAL SEPTAL DEFECT TYPE 3, CARDIOMYOPATHY DILATED TYPE 1EE, CARDIOMYOPATHY FAMILIAL HYPERTROPHIC TYPE 14