MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Triplets
[NCBI]
Gene
Gene
Link
Information
Gain
01
WFS2
[NCBI]
0.000198622
AFP
[NCBI]
8.96202e-06
PIH
[NCBI]
5.17304e-06
G6PD
[NCBI]
4.32102e-06
KIF20B
[NCBI]
3.63064e-06
CFTR
[NCBI]
3.09897e-06
NAMPT
[NCBI]
3.04973e-06
COL7A1
[NCBI]
2.98095e-06
CYP27A1
[NCBI]
2.54004e-06
SIRT1
[NCBI]
2.4425e-06
CYP19A1
[NCBI]
2.41568e-06
ERCC2
[NCBI]
2.19368e-06
TROVE2
[NCBI]
2.18623e-06
FMR1
[NCBI]
1.93451e-06
TGFB1
[NCBI]
1.41125e-06
EGF
[NCBI]
8.36091e-07
OMIM
OMIM
Link
Information
gain
01
otitis media, susceptibility to
[NCBI]
0.000990675
ANON1
[NCBI]
0.000844761
NLS
[NCBI]
0.00067303
chiari malformation type i
[NCBI]
0.000663058
diabetes mellitus, transient neonatal, 1
[NCBI]
0.000635982
COFS2
[NCBI]
0.000175153
WFS2
[NCBI]
0.000147382
cahmr syndrome
[NCBI]
0.000147382
xeroderma pigmentosum ix
[NCBI]
0.000136902
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
[NCBI]
0.000136902
martsolf syndrome
[NCBI]
0.000130098
CPI
[NCBI]
0.00012991
oeis complex
[NCBI]
0.000121008
xeroderma pigmentosum, complementation group e
[NCBI]
0.000117656
de sanctis-cacchione syndrome
[NCBI]
0.000114787
XPG
[NCBI]
0.000110052
XPV
[NCBI]
0.000108048
XPF
[NCBI]
0.000106227
XPD
[NCBI]
0.000104559
COFS1
[NCBI]
0.000103019
PHA
[NCBI]
9.90064e-05
TTDP
[NCBI]
9.67197e-05
EFE
[NCBI]
9.19412e-05
WFS1
[NCBI]
8.37122e-05
XPA
[NCBI]
8.01278e-05
CSA
[NCBI]
7.83378e-05
AFP
[NCBI]
6.87816e-05
krabbe disease
[NCBI]
6.42771e-05
ORM1
[NCBI]
3.55812e-05
XPC
[NCBI]
3.35028e-05
ERCC2
[NCBI]
3.31254e-05
ERCC5
[NCBI]
3.26008e-05
G6PD
[NCBI]
3.19095e-05
COL7A1
[NCBI]
3.06263e-05
thrombocytopenic purpura, autoimmune
[NCBI]
2.30425e-05
CF
[NCBI]
1.01064e-05
VEGF
[NCBI]
1.824e-06
EGF
[NCBI]
1.48037e-06
SLE
[NCBI]
4.16202e-07
Database Center for Life Science