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01 Cardiomyopathy, Hypertrophic [NCBI]


Gene


Gene Link Information
Gain
01
MYH7 [NCBI] 0.000715082
MYBPC3 [NCBI] 0.000480147
TRNV [NCBI] 0.000438875
TNNT2 [NCBI] 0.00031756
TPM1 [NCBI] 0.00017651
TNNI3 [NCBI] 0.000146157
MYL2 [NCBI] 0.00010466
PLN [NCBI] 8.44663e-05
CSRP3 [NCBI] 8.22401e-05
MYL3 [NCBI] 6.97241e-05
SCO2 [NCBI] 6.88498e-05
PRKAG2 [NCBI] 5.55154e-05
MYH6 [NCBI] 5.47075e-05
PTPN11 [NCBI] 5.07354e-05
TNNC1 [NCBI] 5.00416e-05
ACTC1 [NCBI] 4.5875e-05
MYO1A [NCBI] 4.46443e-05
FXN [NCBI] 3.94235e-05
JPH2 [NCBI] 3.67528e-05
TCAP [NCBI] 3.53025e-05
TTN [NCBI] 3.42014e-05
NPPB [NCBI] 3.06415e-05
VCL [NCBI] 2.63946e-05
LAMP2 [NCBI] 2.11578e-05
OBSCN [NCBI] 1.98829e-05
TNNI1 [NCBI] 1.88892e-05
HAND1 [NCBI] 1.57425e-05
MEF2C [NCBI] 1.54162e-05
MEF2A [NCBI] 1.45914e-05
BNIP3L [NCBI] 1.44715e-05
AGT [NCBI] 1.36529e-05
MYBPC2 [NCBI] 1.35328e-05
NRAP [NCBI] 1.35328e-05
ACE2 [NCBI] 1.26138e-05
MYOM2 [NCBI] 1.24156e-05
RCAN1 [NCBI] 1.20511e-05
MTPN [NCBI] 1.19941e-05
MYBPH [NCBI] 1.11529e-05
MYBPC1 [NCBI] 1.11529e-05
SLC25A3 [NCBI] 1.02551e-05
KBTBD10 [NCBI] 1.02551e-05
COX15 [NCBI] 9.67224e-06
ATP6V1G2 [NCBI] 9.67224e-06
MLYCD [NCBI] 9.67224e-06
STK19 [NCBI] 9.67224e-06
IRX4 [NCBI] 9.67224e-06
MRPS22 [NCBI] 9.67224e-06
CYP11B2 [NCBI] 9.35809e-06
AHNAK [NCBI] 9.23901e-06
LHX2 [NCBI] 8.89389e-06
SYNC [NCBI] 8.89389e-06
MYOZ2 [NCBI] 8.3615e-06
NDUFV2 [NCBI] 8.3615e-06
MYOCD [NCBI] 8.3615e-06
PVALB [NCBI] 8.14694e-06
TNNT1 [NCBI] 8.14694e-06
GNAI1 [NCBI] 8.14694e-06
PPP3R1 [NCBI] 8.14694e-06
GYS1 [NCBI] 7.62937e-06
DLD [NCBI] 7.48675e-06
BAT1 [NCBI] 7.35518e-06
HOPX [NCBI] 7.35518e-06
DAG1 [NCBI] 7.26828e-06
SURF1 [NCBI] 7.23307e-06
SGCD [NCBI] 7.01241e-06
ACTN2 [NCBI] 7.01241e-06
ACADVL [NCBI] 6.91199e-06
LDB3 [NCBI] 6.91199e-06
EDN2 [NCBI] 6.91199e-06
ACTN1 [NCBI] 6.72742e-06
HDAC5 [NCBI] 6.72742e-06
KCNQ1 [NCBI] 6.66514e-06
SSPN [NCBI] 6.48359e-06
HAND2 [NCBI] 6.48359e-06
CACNA1C [NCBI] 6.40955e-06
VDAC1 [NCBI] 6.40955e-06
DMPK [NCBI] 6.30393e-06
PRKAA1 [NCBI] 6.20516e-06
MYO6 [NCBI] 6.0815e-06
FHL2 [NCBI] 5.96632e-06
MICB [NCBI] 5.91157e-06
CDK9 [NCBI] 5.91157e-06
ADRBK1 [NCBI] 5.91157e-06
ACE [NCBI] 5.90021e-06
NFKBIL1 [NCBI] 5.85855e-06
TGFB1 [NCBI] 5.72312e-06
RHEB [NCBI] 5.66181e-06
PMM2 [NCBI] 5.66181e-06
ND1 [NCBI] 5.48582e-06
DES [NCBI] 5.40434e-06
AHSG [NCBI] 5.32667e-06
APBA1 [NCBI] 5.32667e-06
MUC16 [NCBI] 5.28916e-06
PRKACA [NCBI] 5.18145e-06
PLA2G7 [NCBI] 5.11336e-06
GATA4 [NCBI] 5.11336e-06
MAP2K6 [NCBI] 5.08033e-06
MAP3K5 [NCBI] 4.89498e-06
CAV3 [NCBI] 4.86602e-06
TTR [NCBI] 4.82164e-06
NOS3 [NCBI] 4.70674e-06
RAF1 [NCBI] 4.70224e-06
GLA [NCBI] 4.67647e-06
CRYAB [NCBI] 4.57727e-06
REN [NCBI] 4.52985e-06
RYR1 [NCBI] 4.41702e-06
CD36 [NCBI] 4.374e-06
SRF [NCBI] 4.35291e-06
FGA [NCBI] 4.31154e-06
CXCL11 [NCBI] 4.31154e-06
MYH9 [NCBI] 4.19345e-06
ATP2A2 [NCBI] 4.08345e-06
NKX2-5 [NCBI] 4.01411e-06
GJA1 [NCBI] 3.99723e-06
HLA-DPB1 [NCBI] 3.98053e-06
GAA [NCBI] 3.96401e-06
TIMP2 [NCBI] 3.86832e-06
NPPA [NCBI] 3.69276e-06
PRKCE [NCBI] 3.67898e-06
CS [NCBI] 3.66532e-06
PPARGC1A [NCBI] 3.44971e-06
MICA [NCBI] 3.36898e-06
IGFBP1 [NCBI] 3.28164e-06
IGF1R [NCBI] 3.06449e-06
GNAS [NCBI] 2.78845e-06
CYP19A1 [NCBI] 2.67832e-06
ESR2 [NCBI] 2.58262e-06
HRAS [NCBI] 2.56336e-06
CP [NCBI] 2.53068e-06
DDIT3 [NCBI] 2.51168e-06
LMNA [NCBI] 2.44414e-06
IGFBP3 [NCBI] 2.36264e-06
NOS1 [NCBI] 2.24878e-06
PDE5A [NCBI] 2.09646e-06
PRKCA [NCBI] 2.00672e-06
PRKCB [NCBI] 1.88673e-06
MMP2 [NCBI] 1.63714e-06
IGF1 [NCBI] 1.59285e-06
CTNNB1 [NCBI] 1.3104e-06
ESR1 [NCBI] 1.00103e-06
CCL2 [NCBI] 9.47802e-07
APC [NCBI] 6.30845e-07
PCNA [NCBI] 6.2998e-07
TNF [NCBI] 4.19541e-07
CAT [NCBI] 4.16666e-07
HGF [NCBI] 1.6291e-07
BAX [NCBI] 3.81927e-08
AR [NCBI] 2.838e-08
VWF [NCBI] 2.7846e-08
FASLG [NCBI] 1.99568e-08
AFP [NCBI] 8.44361e-09




OMIM


OMIM Link Information
gain
01
CMH [NCBI] 0.0103978
cataract and cardiomyopathy [NCBI] 0.00462338
MYH7 [NCBI] 0.00168858
CMH4 [NCBI] 0.000891517
MYBPC3 [NCBI] 0.000830729
TNNT2 [NCBI] 0.000792063
CMH3 [NCBI] 0.000395411
costello syndrome [NCBI] 0.000356882
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome [NCBI] 0.000318027
TPM1 [NCBI] 0.000294909
leopard syndrome 1 [NCBI] 0.000273383
SLE [NCBI] 0.000263709
wolff-parkinson-white syndrome [NCBI] 0.000249992
danon disease [NCBI] 0.000233753
TNNI3 [NCBI] 0.000230353
CMH10 [NCBI] 0.000197544
subaortic stenosis--short stature syndrome [NCBI] 0.000197544
MYL2 [NCBI] 0.00017484
FRDA [NCBI] 0.000163659
SCO2 [NCBI] 0.000155707
PRKAG2 [NCBI] 0.000151381
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency [NCBI] 0.000143104
EFE [NCBI] 0.000134561
RCM1 [NCBI] 0.000124836
fibromuscular dysplasia of arteries [NCBI] 0.000102536
COXPD5 [NCBI] 9.87317e-05
mitochondrial phosphate carrier deficiency [NCBI] 9.87317e-05
leopard syndrome 2 [NCBI] 9.87317e-05
pulmonic stenosis and deafness [NCBI] 9.87317e-05
CMH2 [NCBI] 9.87317e-05
pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities [NCBI] 9.87317e-05
HRAS [NCBI] 9.71283e-05
MYH6 [NCBI] 9.41096e-05
LAMP2 [NCBI] 8.91044e-05
MTTI [NCBI] 8.91044e-05
SGCD [NCBI] 8.51196e-05
NS1 [NCBI] 8.24588e-05
SLC25A20 [NCBI] 7.77016e-05
subaortic stenosis, membranous [NCBI] 7.62957e-05
DFNA22 [NCBI] 7.62957e-05
glycogen storage disease 0, muscle [NCBI] 7.62957e-05
NS5 [NCBI] 7.62957e-05
mental and growth retardation with amblyopia [NCBI] 7.62957e-05
CMH8 [NCBI] 7.62957e-05
creases, infra-auricular cutaneous, with tall stature and advanced bone age [NCBI] 7.62957e-05
CDSP [NCBI] 7.54066e-05
TTN [NCBI] 7.43087e-05
mitochondrial complex iv deficiency [NCBI] 7.35714e-05
LDHCP [NCBI] 6.78502e-05
CMD1L [NCBI] 6.78502e-05
PLN [NCBI] 6.59883e-05
glycogen storage disease of heart, lethal congenital [NCBI] 6.23785e-05
glutamate monosodium sensitivity [NCBI] 6.23785e-05
alpha-b crystallinopathy [NCBI] 6.23785e-05
MEF2C [NCBI] 5.5579e-05
SLC25A3 [NCBI] 5.5579e-05
VCL [NCBI] 5.5579e-05
MYOZ2 [NCBI] 5.5579e-05
TNNC1 [NCBI] 5.5579e-05
MYL3 [NCBI] 5.5579e-05
mitochondrial complex ii deficiency [NCBI] 5.2414e-05
VDAC1 [NCBI] 5.03868e-05
NDUFV2 [NCBI] 5.03868e-05
TNNT3 [NCBI] 5.03868e-05
HDAC5 [NCBI] 5.03868e-05
MRPS22 [NCBI] 5.03868e-05
SVAS [NCBI] 4.76805e-05
COX15 [NCBI] 4.70182e-05
CDK9 [NCBI] 4.70182e-05
sarcosinemia [NCBI] 4.63637e-05
MTTL1 [NCBI] 4.62791e-05
MTPN [NCBI] 4.45157e-05
MTTG [NCBI] 4.45157e-05
ACTC1 [NCBI] 4.08681e-05
NPPB [NCBI] 4.08681e-05
GYS1 [NCBI] 4.08681e-05
MLYCD [NCBI] 4.08681e-05
MEF2A [NCBI] 3.94523e-05
acyl-coa dehydrogenase, very long-chain, deficiency of [NCBI] 3.76659e-05
fabry disease [NCBI] 3.71944e-05
RAF1 [NCBI] 3.71182e-05
MYO6 [NCBI] 3.5236e-05
ACADVL [NCBI] 3.36597e-05
PRKCM [NCBI] 3.36597e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 3.2857e-05
infantile sialic acid storage disorder [NCBI] 3.03507e-05
myopathy, myofibrillar, desmin-related [NCBI] 3.03507e-05
CYP11B2 [NCBI] 3.00586e-05
mitochondrial complex i deficiency [NCBI] 2.97868e-05
CRYAB [NCBI] 2.95706e-05
central core disease of muscle [NCBI] 2.92444e-05
PMM2 [NCBI] 2.78354e-05
AKT1 [NCBI] 2.70738e-05
MTND1 [NCBI] 2.67148e-05
CAV3 [NCBI] 2.63689e-05
glycogen storage disease iii [NCBI] 2.63671e-05
cardiofaciocutaneous syndrome [NCBI] 2.39877e-05
SLC11A2 [NCBI] 2.39833e-05
MTATP6 [NCBI] 2.32259e-05
CMD1A [NCBI] 2.29392e-05
BMD [NCBI] 2.19681e-05
DMPK [NCBI] 2.16687e-05
TNF [NCBI] 2.14192e-05
CDG1A [NCBI] 2.13588e-05
NOS3 [NCBI] 2.1075e-05
FXN [NCBI] 2.06997e-05
MAP3K5 [NCBI] 1.93383e-05
FGA [NCBI] 1.81583e-05
VEGF [NCBI] 1.62687e-05
LMNA [NCBI] 1.50634e-05
glycogen storage disease ii [NCBI] 1.26458e-05
LS [NCBI] 1.25063e-05
WT1 [NCBI] 1.18363e-05
TTR [NCBI] 1.14953e-05
CP [NCBI] 7.6659e-06
NPPA [NCBI] 6.06969e-06
NF1 [NCBI] 4.90919e-06
leber optic atrophy [NCBI] 4.64023e-06
AFP [NCBI] 4.07174e-06
WBS [NCBI] 4.01974e-06
HGF [NCBI] 7.29236e-07
PCNA [NCBI] 4.8652e-07
CAT [NCBI] 2.80808e-08




Database Center for Life Science