MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Randomized Controlled Trials as Topic
[NCBI]
Gene
Gene
Link
Information
Gain
01
OMIM
OMIM
Link
Information
gain
01
RA
[NCBI]
0.00243682
MDD
[NCBI]
0.00136211
apnea, obstructive sleep
[NCBI]
0.000835316
CRC
[NCBI]
0.000458695
KLK3
[NCBI]
0.000396467
aspirin resistance
[NCBI]
0.000290309
SLE
[NCBI]
0.000153817
GNRH1
[NCBI]
0.000148148
VRNI
[NCBI]
0.000146487
EPO
[NCBI]
0.000146091
EGFR
[NCBI]
0.000139511
PTH
[NCBI]
0.000109661
CF
[NCBI]
9.01621e-05
CJD
[NCBI]
4.32093e-05
MG
[NCBI]
3.77584e-05
TNNT2
[NCBI]
3.75809e-05
chromosome 5q deletion syndrome
[NCBI]
3.13394e-05
TYMS
[NCBI]
2.99967e-05
neural tube defects, folate-sensitive
[NCBI]
2.89809e-05
PWS
[NCBI]
2.82579e-05
RP
[NCBI]
2.65606e-05
AD
[NCBI]
2.52882e-05
PD
[NCBI]
2.42313e-05
VEGF
[NCBI]
2.12711e-05
TNF
[NCBI]
2.10038e-05
NGFB
[NCBI]
2.08514e-05
ALOX5AP
[NCBI]
1.81843e-05
MGMT
[NCBI]
1.81843e-05
BIRC5
[NCBI]
1.55207e-05
CRP
[NCBI]
1.52894e-05
SLC22A6
[NCBI]
1.44494e-05
TGFBR2
[NCBI]
1.40726e-05
CD40LG
[NCBI]
1.40726e-05
TNFSF13B
[NCBI]
1.32298e-05
LTA
[NCBI]
1.29259e-05
TFPI
[NCBI]
1.2808e-05
MMP3
[NCBI]
1.22332e-05
TCF7L2
[NCBI]
1.16196e-05
glioma of brain, familial
[NCBI]
1.13768e-05
PCNA
[NCBI]
1.01185e-05
LCN2
[NCBI]
1.00314e-05
GPT
[NCBI]
9.70044e-06
THPO
[NCBI]
9.54272e-06
ARMD1
[NCBI]
8.94082e-06
MTR
[NCBI]
8.68858e-06
PGR
[NCBI]
8.12574e-06
temporal arteritis
[NCBI]
6.69085e-06
CFH
[NCBI]
6.60683e-06
BDNF
[NCBI]
6.39416e-06
CRH
[NCBI]
6.23341e-06
alopecia, androgenetic
[NCBI]
6.12428e-06
BGLAP
[NCBI]
5.60416e-06
AGER
[NCBI]
5.60416e-06
SOD2
[NCBI]
5.1916e-06
AR
[NCBI]
5.16632e-06
CGD
[NCBI]
4.89589e-06
polycystic kidneys
[NCBI]
4.79786e-06
APOE
[NCBI]
4.73522e-06
NPPA
[NCBI]
4.67559e-06
lymphoma, non-hodgkin, familial
[NCBI]
4.43807e-06
PEDF
[NCBI]
4.24857e-06
SST
[NCBI]
4.22543e-06
COMT
[NCBI]
4.00371e-06
JAK2
[NCBI]
3.71175e-06
MBP
[NCBI]
3.53102e-06
TH
[NCBI]
3.51267e-06
CNTF
[NCBI]
3.30263e-06
VDR
[NCBI]
3.17957e-06
ACPP
[NCBI]
3.09902e-06
GHR
[NCBI]
2.81868e-06
ADHD
[NCBI]
2.662e-06
ACHE
[NCBI]
2.53504e-06
CEACAM5
[NCBI]
2.39734e-06
CFTR
[NCBI]
2.38868e-06
hypercholesterolemia, autosomal dominant
[NCBI]
2.24837e-06
CCK
[NCBI]
2.06912e-06
MBL2
[NCBI]
2.063e-06
F3
[NCBI]
2.02147e-06
PPARA
[NCBI]
1.82366e-06
PRL
[NCBI]
1.52539e-06
GHRH
[NCBI]
1.4788e-06
GAL
[NCBI]
1.34338e-06
ABCC1
[NCBI]
1.13528e-06
PF4
[NCBI]
9.58826e-07
ACE
[NCBI]
9.29622e-07
FGF7
[NCBI]
8.78712e-07
AVP
[NCBI]
8.35087e-07
MPO
[NCBI]
5.88642e-07
TLR4
[NCBI]
5.76214e-07
hla-d histocompatibility type
[NCBI]
4.61265e-07
AFP
[NCBI]
4.14426e-07
APC
[NCBI]
2.91156e-07
HD
[NCBI]
2.73153e-07
HGF
[NCBI]
1.49454e-07
GIST
[NCBI]
1.43099e-07
PTHLH
[NCBI]
1.39795e-07
thrombocytopenic purpura, autoimmune
[NCBI]
1.03951e-07
FRAP1
[NCBI]
9.93168e-08
TTR
[NCBI]
5.99058e-08
TF
[NCBI]
3.33683e-08
TNFRSF11B
[NCBI]
2.96256e-08
GAPDH
[NCBI]
1.0731e-08
Database Center for Life Science