TNNI3

troponin I3, cardiac type
OMIM: 191044
PanelMode of inheritanceDetails
3 panels
R-numbers: R135
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Hypertrophic cardiomyopathy, Cardiomyopathy, familial hypertrophic, 7, Cardiomyopathy, dilated, 1FF, Cardiomyopathy, dilated, 2A,
Component of the following Super Panels:
  • - Sudden unexplained death or survivors of a cardiac event
R-numbers: R132
Signed-off version 2.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Cardiomyopathy, dilated, 1FF (613286), Cardiomyopathy, dilated, 2A,, ?Cardiomyopathy, dilated, 2A (611880), Cardiomyopathy, familial restrictive, 1 (115210), Cardiomyopathy, dilated, 1FF, Cardiomyopathy, hypertrophic, 7 (613690)
Component of the following Super Panels:
  • - Sudden unexplained death or survivors of a cardiac event
R-numbers: R131
Signed-off version 3.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Cardiomyopathy, familial hypertrophic, 7, ?Cardiomyopathy, dilated, 2A (611880), Cardiomyopathy, dilated, 1FF (613286), Cardiomyopathy, familial restrictive, 1 (115210), Cardiomyopathy, hypertrophic, 7 (613690)