MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Apoferritins
[NCBI]
Gene
Gene
Link
Information
Gain
01
LOC286463
[NCBI]
0.000251681
FTHL16
[NCBI]
0.000216972
FTLL1
[NCBI]
0.000195365
FTH1
[NCBI]
1.9269e-05
FTL
[NCBI]
1.8478e-05
MS
[NCBI]
1.37638e-05
FTMT
[NCBI]
1.30794e-05
TFRC
[NCBI]
8.43932e-06
RPL17L1
[NCBI]
3.17051e-06
RPL7AL1
[NCBI]
3.17051e-06
RPS3L1
[NCBI]
3.17051e-06
RPS17L3
[NCBI]
3.17051e-06
NARFL
[NCBI]
2.44721e-06
CYBRD1
[NCBI]
2.05834e-06
ACO1
[NCBI]
1.96348e-06
PIAS3
[NCBI]
1.87577e-06
TP53
[NCBI]
1.85203e-06
NFYA
[NCBI]
1.81436e-06
CUGBP1
[NCBI]
1.79668e-06
SLC40A1
[NCBI]
1.78825e-06
ATF1
[NCBI]
1.78414e-06
TFR2
[NCBI]
1.58009e-06
DMRT1
[NCBI]
1.56709e-06
CD47
[NCBI]
1.50297e-06
THBS1
[NCBI]
1.48373e-06
SUMO1
[NCBI]
1.4478e-06
RAB11A
[NCBI]
1.37966e-06
FXN
[NCBI]
1.32325e-06
CP
[NCBI]
1.26481e-06
AMBP
[NCBI]
1.25452e-06
CIITA
[NCBI]
1.23663e-06
ENG
[NCBI]
1.19679e-06
MYC
[NCBI]
1.13152e-06
HMOX1
[NCBI]
1.10344e-06
TF
[NCBI]
1.04837e-06
HFE
[NCBI]
9.80436e-07
CXCL12
[NCBI]
9.5361e-07
TLR4
[NCBI]
8.74563e-07
NOS2
[NCBI]
8.27604e-07
TNF
[NCBI]
3.91349e-07
OMIM
OMIM
Link
Information
gain
01
hyperferritinemia-cataract syndrome
[NCBI]
0.000360322
basal ganglia disease, adult-onset
[NCBI]
0.000169613
hemochromatosis, neonatal
[NCBI]
0.000165798
FTL
[NCBI]
0.000108825
ACO1
[NCBI]
3.42105e-05
FTH1
[NCBI]
3.26246e-05
HAMP
[NCBI]
3.21021e-05
SLC40A1
[NCBI]
2.97296e-05
TFRC
[NCBI]
2.68418e-05
HFE
[NCBI]
2.04843e-05
CP
[NCBI]
1.63296e-05
TLR4
[NCBI]
1.43118e-05
TF
[NCBI]
1.2103e-05
TNF
[NCBI]
1.12121e-06
Database Center for Life Science