MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Carrier State
[NCBI]
Gene
Gene
Link
Information
Gain
01
OMIM
OMIM
Link
Information
gain
01
RP23
[NCBI]
0.00189937
CF
[NCBI]
0.000458984
cirrhosis, familial
[NCBI]
0.000141555
ruvalcaba syndrome
[NCBI]
9.65415e-05
AFP
[NCBI]
9.61737e-05
hunter-mcalpine craniosynostosis syndrome
[NCBI]
9.14963e-05
ALD
[NCBI]
8.88578e-05
hemochromatosis, neonatal
[NCBI]
8.41415e-05
hepatitis b virus, susceptibility to
[NCBI]
7.65789e-05
CMT4D
[NCBI]
7.65789e-05
von willebrand disease, recessive form
[NCBI]
7.27822e-05
IFNA1
[NCBI]
7.03577e-05
ICP
[NCBI]
6.56311e-05
hepatitis c virus, susceptibility to
[NCBI]
6.04118e-05
hepatocellular carcinoma
[NCBI]
5.70608e-05
PARK2
[NCBI]
5.23195e-05
CTNS
[NCBI]
4.95373e-05
aHUS
[NCBI]
4.95373e-05
LAD
[NCBI]
4.66655e-05
TNF
[NCBI]
4.60929e-05
TMEM142C
[NCBI]
4.25497e-05
TMEM142B
[NCBI]
4.25497e-05
ND
[NCBI]
3.94264e-05
SMA1
[NCBI]
3.64126e-05
CGD
[NCBI]
3.54328e-05
TMEM142A
[NCBI]
3.47185e-05
TLR2
[NCBI]
3.36703e-05
IL10RB
[NCBI]
3.28717e-05
IFNAR2
[NCBI]
3.28717e-05
WHS
[NCBI]
3.23828e-05
FFI
[NCBI]
3.23828e-05
PDE11A
[NCBI]
3.21273e-05
neuraminidase deficiency with beta-galactosidase deficiency
[NCBI]
2.41726e-05
PTPRC
[NCBI]
2.30201e-05
SMN2
[NCBI]
2.27285e-05
ITGB2
[NCBI]
2.10152e-05
leber optic atrophy
[NCBI]
2.06753e-05
SMN1
[NCBI]
1.79559e-05
HNF1A
[NCBI]
1.78937e-05
GCK
[NCBI]
1.78322e-05
CJD
[NCBI]
1.63854e-05
von willebrand disease
[NCBI]
1.60595e-05
VDR
[NCBI]
1.37379e-05
DMD
[NCBI]
1.33723e-05
PLG
[NCBI]
1.26724e-05
HP
[NCBI]
8.77785e-06
APOE
[NCBI]
8.30489e-06
IL2
[NCBI]
7.94572e-06
PTHLH
[NCBI]
6.66855e-06
RA
[NCBI]
6.08299e-06
TF
[NCBI]
6.07363e-06
SHBG
[NCBI]
5.27381e-06
AD
[NCBI]
4.53889e-06
CD
[NCBI]
4.45975e-06
TNFSF6
[NCBI]
3.43996e-06
SLE
[NCBI]
2.90234e-06
LPL
[NCBI]
1.94767e-06
VEGF
[NCBI]
1.37036e-06
AR
[NCBI]
1.09988e-06
ACHE
[NCBI]
3.41075e-07
MG
[NCBI]
9.11324e-08
Database Center for Life Science