TNNT2

troponin T2, cardiac type
OMIM: 191045
PanelMode of inheritanceDetails
3 panels
R-numbers: R135
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Cardiomyopathy, dilated, 1D, Cardiomyopathy, familial hypertrophic, 2, Hypertrophic cardiomyopathy, Left ventricular noncompaction 6,
Component of the following Super Panels:
  • - Sudden cardiac death
R-numbers: R132
Signed-off version 1.6
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Cardiomyopathy, dilated, 1D, Cardiomyopathy, familial restrictive, 3 (612422), Cardiomyopathy, hypertrophic, 2 (115195), Cardiomyopathy, dilated, 1D (601494), Left ventricular noncompaction 6 (601494)
Component of the following Super Panels:
  • - Sudden cardiac death
R-numbers: R131
Signed-off version 2.11
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Cardiomyopathy, familial restrictive, 3 (612422), Cardiomyopathy, hypertrophic, 2 (115195), Cardiomyopathy, dilated, 1D (601494), Cardiomyopathy, familial hypertrophic, 2, Left ventricular noncompaction 6 (601494)