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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