MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hyperpigmentation
[NCBI]
Gene
Gene
Link
Information
Gain
01
DUH
[NCBI]
0.000791042
DCT
[NCBI]
3.6753e-05
KRT5
[NCBI]
2.87228e-05
KITLG
[NCBI]
2.17412e-05
OCA2
[NCBI]
1.94541e-05
DKC1
[NCBI]
1.91867e-05
KRT24
[NCBI]
1.7613e-05
PRKAR1A
[NCBI]
1.75752e-05
TYRP1
[NCBI]
1.73675e-05
SLC29A3
[NCBI]
1.52326e-05
FOXQ1
[NCBI]
1.43341e-05
ECEL1
[NCBI]
1.33169e-05
MRAP
[NCBI]
1.26837e-05
PRM2
[NCBI]
9.45985e-06
ABCG5
[NCBI]
9.381e-06
ABCG8
[NCBI]
9.30562e-06
AAAS
[NCBI]
9.23342e-06
HFE2
[NCBI]
8.85449e-06
ADAR
[NCBI]
8.54449e-06
EDA
[NCBI]
7.96842e-06
KRT14
[NCBI]
7.29492e-06
MITF
[NCBI]
6.77998e-06
PIK3CA
[NCBI]
6.76331e-06
KIT
[NCBI]
6.48121e-06
IKBKE
[NCBI]
6.13346e-06
CHUK
[NCBI]
5.95993e-06
IKBKB
[NCBI]
5.94966e-06
FGFR3
[NCBI]
5.2932e-06
TROVE2
[NCBI]
5.1351e-06
CD38
[NCBI]
4.95944e-06
HFE
[NCBI]
3.70346e-06
NOS2
[NCBI]
3.33256e-06
HGF
[NCBI]
3.26956e-06
TP53
[NCBI]
2.627e-06
OMIM
OMIM
Link
Information
gain
01
DDD
[NCBI]
0.00129818
BZX
[NCBI]
0.00105062
IP
[NCBI]
0.000214441
DKC
[NCBI]
0.0002068
DPR
[NCBI]
0.000190534
naegeli syndrome
[NCBI]
0.000184562
dyschromatosis symmetrica hereditaria 1
[NCBI]
0.000135791
follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts
[NCBI]
0.000125989
FDH
[NCBI]
0.000120065
hyperkeratosis-hyperpigmentation syndrome
[NCBI]
0.000103524
KRT24
[NCBI]
9.81269e-05
PEPB
[NCBI]
9.81269e-05
aplasia cutis congenita with epibulbar dermoids
[NCBI]
8.22e-05
IHCM
[NCBI]
7.51504e-05
EBS-MP
[NCBI]
6.89205e-05
DKC1
[NCBI]
5.86684e-05
GJB3
[NCBI]
5.68152e-05
KRT14
[NCBI]
5.60041e-05
KRT5
[NCBI]
5.48997e-05
IKBKG
[NCBI]
5.48997e-05
AHC
[NCBI]
5.40622e-05
DAR
[NCBI]
5.30777e-05
FPLD2
[NCBI]
5.30777e-05
RTS
[NCBI]
4.5042e-05
IGFALS
[NCBI]
4.4726e-05
mucopolysaccharidosis type ii
[NCBI]
4.20199e-05
HGPS
[NCBI]
4.0188e-05
EV
[NCBI]
2.92118e-05
PJS
[NCBI]
2.38599e-05
GIST
[NCBI]
1.86277e-05
AS
[NCBI]
1.80185e-05
SLE
[NCBI]
1.64323e-05
PWS
[NCBI]
8.62433e-06
Database Center for Life Science