Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Retinitis [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science