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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cardiomyopathy, Hypertrophic, Familial [NCBI]

Gene


 Gene Link Information
Gain		 01
MYH7 [NCBI] 0.000239528
TNNI3 [NCBI] 0.000117574
MYBPC3 [NCBI] 0.000117258
TNNT2 [NCBI] 8.60604e-05
TPM1 [NCBI] 5.37618e-05
TNNC1 [NCBI] 3.52078e-05
MYL3 [NCBI] 2.39212e-05
ACTC1 [NCBI] 2.04084e-05
C15orf24 [NCBI] 1.62432e-05
MYL9 [NCBI] 1.38629e-05
TNNI3K [NCBI] 1.38629e-05
MCM10 [NCBI] 1.19474e-05
AGTR1 [NCBI] 1.16378e-05
MYOZ2 [NCBI] 1.10683e-05
SLN [NCBI] 1.08533e-05
PLN [NCBI] 1.07296e-05
TMOD1 [NCBI] 1.04903e-05
MYL2 [NCBI] 9.9363e-06
SRI [NCBI] 9.26065e-06
SCO2 [NCBI] 8.96814e-06
TTN [NCBI] 8.77752e-06
CALR [NCBI] 8.71843e-06
PRKAG2 [NCBI] 8.71843e-06
CASQ2 [NCBI] 8.60604e-06
CMA1 [NCBI] 8.55251e-06
TPM3 [NCBI] 8.26236e-06
LAMP2 [NCBI] 7.83226e-06
CAV3 [NCBI] 7.54658e-06
PVR [NCBI] 6.65719e-06
DSP [NCBI] 6.60607e-06
CYP11B2 [NCBI] 6.16539e-06
KCNQ1 [NCBI] 4.79119e-06
PTPN11 [NCBI] 4.55453e-06
PRKCA [NCBI] 4.53991e-06
AGT [NCBI] 3.71533e-06
ACE [NCBI] 2.69691e-06
NOS3 [NCBI] 2.27204e-06



OMIM


 OMIM Link Information
gain		 01
cataract and cardiomyopathy [NCBI] 0.00111789
danon disease [NCBI] 0.000219496
CMH8 [NCBI] 0.000137921
TNNT2 [NCBI] 0.000116065
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome [NCBI] 0.00011386
MYH7 [NCBI] 0.000102686
wolff-parkinson-white syndrome [NCBI] 9.97657e-05
MYL3 [NCBI] 7.92643e-05
SRI [NCBI] 7.40637e-05
HEY2 [NCBI] 7.06867e-05
MYL2 [NCBI] 6.81758e-05
TNNI3 [NCBI] 6.45112e-05
SLN [NCBI] 6.45112e-05
CMH [NCBI] 6.2906e-05
PRKAG2 [NCBI] 6.18421e-05
LAMP2 [NCBI] 6.07361e-05
SLC25A4 [NCBI] 5.26231e-05
CAV3 [NCBI] 4.98266e-05
PLN [NCBI] 4.94846e-05



Database Center for Life Science