Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Retinitis	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	5.28348e-05
MC5R	[NCBI]	2.9278e-05
TNF	[NCBI]	2.14697e-05
RLBP1	[NCBI]	2.03704e-05
GFAP	[NCBI]	2.02855e-05
SELPLG	[NCBI]	1.52958e-05
CD200R1	[NCBI]	1.28585e-05
RDH5	[NCBI]	1.05163e-05
VIP	[NCBI]	1.05095e-05
DPYSL5	[NCBI]	1.04383e-05
IFNB1	[NCBI]	9.43001e-06
SIGLEC1	[NCBI]	9.43001e-06
PLD1	[NCBI]	8.85929e-06
NOS2	[NCBI]	8.78572e-06
TIMP3	[NCBI]	7.72641e-06
CXCL9	[NCBI]	6.95991e-06
CXCL10	[NCBI]	6.64322e-06
TJP1	[NCBI]	6.18369e-06
IFNGR1	[NCBI]	4.97824e-06
CD68	[NCBI]	3.42483e-06
MBP	[NCBI]	3.2012e-06
VWF	[NCBI]	2.71099e-06
NGF	[NCBI]	2.63263e-06
MPO	[NCBI]	2.60899e-06
VEGFA	[NCBI]	2.52952e-06

OMIM	Link	Information gain
VRNI	[NCBI]	0.000994076
woolly hair, autosomal dominant	[NCBI]	0.00088464
MC5R	[NCBI]	0.000170053
EVR1	[NCBI]	0.000155071
panencephalitis, subacute sclerosing	[NCBI]	0.000151725
ABL	[NCBI]	0.000126814
fundus dystrophy, pseudoinflammatory, recessive form	[NCBI]	0.000103324
CD200R1	[NCBI]	8.48492e-05
EVR2	[NCBI]	8.34102e-05
fundus albipunctatus	[NCBI]	8.16093e-05
SFD	[NCBI]	7.47703e-05
DHRD	[NCBI]	7.17329e-05
DPYSL5	[NCBI]	7.10704e-05
SLSN1	[NCBI]	6.76781e-05
ALMS	[NCBI]	6.50412e-05
RP1	[NCBI]	6.27781e-05
VEGF	[NCBI]	5.71516e-05
GFAP	[NCBI]	5.52044e-05
bare lymphocyte syndrome, type ii	[NCBI]	5.37602e-05
TNF	[NCBI]	4.63022e-05
TIMP3	[NCBI]	4.35705e-05
MS	[NCBI]	4.08663e-05
VIP	[NCBI]	2.94167e-05
SLE	[NCBI]	1.38565e-05
SPP1	[NCBI]	1.22613e-05
TNFSF6	[NCBI]	8.9325e-06
RA	[NCBI]	8.12746e-06
CRH	[NCBI]	5.3633e-06
MBP	[NCBI]	4.7374e-06
MPO	[NCBI]	2.50195e-06
NGFB	[NCBI]	2.41265e-06