Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyperpigmentation	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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