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MeSH keywords -> Related genes, diseases (OMIM)


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01 Observer Variation [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
IS1 [NCBI] 0.00415888
RA [NCBI] 0.000955721
asperger syndrome, susceptibility to, 1 [NCBI] 0.000795485
palatopharyngeal incompetence [NCBI] 0.000401263
apnea, obstructive sleep [NCBI] 0.00013189
KLK3 [NCBI] 0.000102359
FTD [NCBI] 9.12699e-05
PCNA [NCBI] 7.25066e-05
MDD [NCBI] 6.22375e-05
SCZD4 [NCBI] 5.27937e-05
LIP [NCBI] 4.34534e-05
SLE [NCBI] 4.24127e-05
melanoma, uveal [NCBI] 3.41222e-05
APOE [NCBI] 2.95005e-05
HHF2 [NCBI] 2.94977e-05
ARMD1 [NCBI] 2.71091e-05
TCOF [NCBI] 2.64868e-05
VEGF [NCBI] 2.49857e-05
AVSD [NCBI] 2.3956e-05
AD [NCBI] 1.97223e-05
SLC6A3 [NCBI] 1.92591e-05
ADHD [NCBI] 1.75423e-05
PLAUR [NCBI] 1.63181e-05
MG [NCBI] 1.62763e-05
AR [NCBI] 1.62575e-05
AMH [NCBI] 1.13723e-05
CF [NCBI] 1.11679e-05
PGR [NCBI] 9.1332e-06
leber optic atrophy [NCBI] 8.62211e-06
CPI [NCBI] 7.70005e-06
MUC1 [NCBI] 7.43371e-06
TFPI [NCBI] 7.20008e-06
BL [NCBI] 7.17945e-06
CEACAM5 [NCBI] 6.0739e-06
TNFRSF11B [NCBI] 5.73591e-06
PTH [NCBI] 2.54657e-06
EGF [NCBI] 2.33333e-06
AS [NCBI] 2.1884e-06
CJD [NCBI] 2.05583e-06
TNF [NCBI] 1.72404e-06
PD [NCBI] 1.46793e-06
HGF [NCBI] 1.2505e-06
MPO [NCBI] 1.17867e-06
CRC [NCBI] 1.12761e-06
VIP [NCBI] 7.47902e-07
TS [NCBI] 5.44087e-07
EPO [NCBI] 4.95952e-07
PWS [NCBI] 3.76435e-07
AVP [NCBI] 2.85183e-07
APC [NCBI] 1.74755e-07
CD [NCBI] 1.07641e-08




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