MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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