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MeSH keywords -> Related genes, diseases (OMIM)


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01 Heart Block [NCBI]

Gene


 Gene Link Information
Gain		 01
TROVE2 [NCBI] 0.000884328
NKX2-5 [NCBI] 0.000104792
SCN5A [NCBI] 4.08766e-05
TRIM21 [NCBI] 2.95064e-05
LMNA [NCBI] 2.40347e-05
SSB [NCBI] 1.95765e-05
HCN4 [NCBI] 1.85279e-05
EMD [NCBI] 1.6635e-05
DMPK [NCBI] 1.52722e-05
KCNA7 [NCBI] 1.48377e-05
CRYAB [NCBI] 1.41123e-05
USP4 [NCBI] 1.09761e-05
SYNC [NCBI] 1.0197e-05
RICS [NCBI] 9.9098e-06
SOX6 [NCBI] 9.66395e-06
KCNH6 [NCBI] 9.60077e-06
NGF [NCBI] 9.57434e-06
SP4 [NCBI] 8.5331e-06
MEF2C [NCBI] 7.78085e-06
ANK1 [NCBI] 7.70647e-06
CACNA1C [NCBI] 7.70647e-06
TBX5 [NCBI] 7.50104e-06
CALR [NCBI] 7.31777e-06
KIF11 [NCBI] 7.20573e-06
KCNE2 [NCBI] 6.73529e-06
DES [NCBI] 6.6947e-06
TFAM [NCBI] 6.50521e-06
TNXB [NCBI] 6.40095e-06
ACE2 [NCBI] 6.40095e-06
KCNE1 [NCBI] 5.71792e-06
KCNH2 [NCBI] 4.75673e-06
NR3C1 [NCBI] 4.49073e-06
DMD [NCBI] 4.253e-06
ERG [NCBI] 3.61609e-06
KCNQ1 [NCBI] 3.43584e-06
AHR [NCBI] 3.19271e-06
PF4 [NCBI] 3.08869e-06
TGFB1 [NCBI] 3.04282e-06
HLA-DQB1 [NCBI] 1.95689e-06
HLA-DRB1 [NCBI] 1.4285e-06
CAT [NCBI] 1.30593e-06
TH [NCBI] 1.2522e-06
AVP [NCBI] 1.18996e-06
CD68 [NCBI] 1.09866e-06
NOS2 [NCBI] 9.44085e-07
HIF1A [NCBI] 9.15034e-07
TNF [NCBI] 1.44748e-07



OMIM


 OMIM Link Information
gain		 01
PFHB1B [NCBI] 0.00684053
PFHB2 [NCBI] 0.00279952
PFHB1A [NCBI] 0.00205681
heart block, congenital [NCBI] 0.00184859
heart-hand syndrome, slovenian type [NCBI] 0.0010375
spondylometaphyseal dysplasia, sedaghatian type [NCBI] 0.000644945
KSS [NCBI] 0.000591414
ASD1 [NCBI] 0.000587372
NKX2E [NCBI] 0.000522281
EDMD [NCBI] 0.000406737
SLE [NCBI] 0.000378212
RA [NCBI] 0.000309658
RCM1 [NCBI] 0.00023018
atrial septal defect with atrioventricular conduction defects [NCBI] 0.000223135
SCN5A [NCBI] 0.000185875
atrial standstill [NCBI] 0.000165552
cardiac conduction defect [NCBI] 0.000137669
NPPA [NCBI] 0.000136043
wolff-parkinson-white syndrome [NCBI] 0.000113068
GJA5 [NCBI] 0.000105426
heart-hand syndrome, spanish type [NCBI] 0.000105164
atrioventricular dissociation [NCBI] 0.000105164
EFE [NCBI] 8.88994e-05
hyperoxaluria, primary, type i [NCBI] 8.69822e-05
CKMT1B [NCBI] 8.11133e-05
KCNA7 [NCBI] 8.11133e-05
CMD1A [NCBI] 7.95866e-05
CMT1B [NCBI] 7.1339e-05
TS [NCBI] 6.87751e-05
SP4 [NCBI] 6.73354e-05
LMNA [NCBI] 6.62965e-05
SOX6 [NCBI] 6.21367e-05
CALR [NCBI] 6.21367e-05
CMD1E [NCBI] 5.87744e-05
TFAM [NCBI] 5.87617e-05
LQT3 [NCBI] 4.83099e-05
tetralogy of fallot [NCBI] 4.48951e-05
SIX5 [NCBI] 4.39706e-05
SLC25A20 [NCBI] 4.33517e-05
danon disease [NCBI] 4.1271e-05
EMD [NCBI] 4.07339e-05
EDMD2 [NCBI] 3.97371e-05
brugada syndrome 1 [NCBI] 3.97371e-05
NGFB [NCBI] 3.95905e-05
RYR2 [NCBI] 3.83036e-05
oca2 gene [NCBI] 3.79514e-05
myopathy, myofibrillar, desmin-related [NCBI] 3.64702e-05
dystrophia myotonica 1 [NCBI] 2.9331e-05
DM2 [NCBI] 2.60269e-05
KCNH2 [NCBI] 2.42018e-05
NPS [NCBI] 2.21085e-05
GJA1 [NCBI] 2.07358e-05
AVSD [NCBI] 1.90996e-05
glycogen storage disease ii [NCBI] 1.79818e-05
apnea, obstructive sleep [NCBI] 1.57561e-05
AHR [NCBI] 1.52096e-05
PF4 [NCBI] 1.38852e-05
CMH [NCBI] 1.12862e-05
CAT [NCBI] 4.36551e-06
TH [NCBI] 3.6579e-06
AVP [NCBI] 1.88963e-06
RP [NCBI] 1.31694e-08



Database Center for Life Science