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MeSH keywords -> Related genes, diseases (OMIM)


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01 Population Surveillance [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
DWS [NCBI] 0.0011761
CELIAC5 [NCBI] 0.00101245
CRC [NCBI] 0.000933105
CJD [NCBI] 0.00092308
kala-azar, susceptibility to, 1 [NCBI] 0.000847798
CHDM [NCBI] 0.000847798
constricting bands, congenital [NCBI] 0.000678643
BULN1 [NCBI] 0.000657571
MAFD6 [NCBI] 0.000258666
APC [NCBI] 0.000246992
SLE [NCBI] 0.000188956
KLK3 [NCBI] 0.000184195
CPI [NCBI] 0.000152267
incisors, shovel-shaped [NCBI] 0.000121362
mast syndrome [NCBI] 9.36351e-05
CD [NCBI] 9.1925e-05
aortic valve disease [NCBI] 8.09226e-05
carotid intimal medial thickness 1 [NCBI] 7.64379e-05
TG [NCBI] 7.55005e-05
NN [NCBI] 7.14225e-05
MDD [NCBI] 6.13115e-05
AFP [NCBI] 5.93234e-05
apnea, obstructive sleep [NCBI] 5.73315e-05
RA [NCBI] 5.1804e-05
lymphoma, non-hodgkin, familial [NCBI] 5.17677e-05
brugada syndrome 1 [NCBI] 4.3716e-05
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 3.91562e-05
lung cancer [NCBI] 3.76132e-05
apert syndrome [NCBI] 3.5525e-05
acidic cluster protein, 33-kd [NCBI] 3.4693e-05
APOE [NCBI] 3.39306e-05
gastric cancer [NCBI] 3.36602e-05
PKS [NCBI] 3.30808e-05
malaria, susceptibility to [NCBI] 3.14522e-05
lactase persistence [NCBI] 3.09424e-05
nijmegen breakage syndrome [NCBI] 3.09424e-05
PLA2G1B [NCBI] 2.9978e-05
CEACAM5 [NCBI] 2.83347e-05
thyroid carcinoma, papillary [NCBI] 2.6948e-05
sickle cell anemia [NCBI] 2.58092e-05
BMPR1A [NCBI] 2.34629e-05
ARMD1 [NCBI] 2.31249e-05
Ge [NCBI] 2.27872e-05
MUTYH [NCBI] 2.24765e-05
CES [NCBI] 2.22289e-05
SHBG [NCBI] 2.05068e-05
hypertension, essential [NCBI] 2.00761e-05
TNFRSF10A [NCBI] 2.0039e-05
lynch syndrome i [NCBI] 1.91101e-05
JAG1 [NCBI] 1.8328e-05
FH [NCBI] 1.65591e-05
HP [NCBI] 1.64904e-05
GALT [NCBI] 1.64515e-05
danubian endemic familial nephropathy [NCBI] 1.59972e-05
G6PD [NCBI] 1.59486e-05
GTS [NCBI] 1.50105e-05
DHFR [NCBI] 1.45775e-05
SLC4A1 [NCBI] 1.45664e-05
APOA1 [NCBI] 1.43423e-05
MTR [NCBI] 1.4057e-05
SCZD [NCBI] 1.36477e-05
AR [NCBI] 1.32732e-05
FRDA [NCBI] 1.30532e-05
MAOA [NCBI] 1.21894e-05
CFH [NCBI] 1.18082e-05
CDKN2A [NCBI] 1.14956e-05
LAM [NCBI] 1.08302e-05
BCNS [NCBI] 1.07129e-05
IL6 [NCBI] 1.03333e-05
HBB [NCBI] 1.02431e-05
ACADM [NCBI] 1.01291e-05
TNF [NCBI] 1.00795e-05
hemophilia a [NCBI] 9.86887e-06
APOB [NCBI] 9.82883e-06
HEMB [NCBI] 9.50193e-06
AD [NCBI] 9.29226e-06
FAAH [NCBI] 8.78859e-06
TS [NCBI] 8.16516e-06
RB1 [NCBI] 8.09891e-06
fragile x mental retardation syndrome [NCBI] 7.15988e-06
PJS [NCBI] 7.00402e-06
DFSP [NCBI] 6.92725e-06
SLOS [NCBI] 6.92725e-06
VDR [NCBI] 6.1155e-06
thrombocytopenic purpura, autoimmune [NCBI] 5.67454e-06
ACE [NCBI] 4.65987e-06
CF [NCBI] 4.27965e-06
PD [NCBI] 4.21462e-06
SOD2 [NCBI] 3.71111e-06
LPL [NCBI] 3.19721e-06
RTT [NCBI] 2.69697e-06
RNASE3 [NCBI] 2.60275e-06
SLC6A3 [NCBI] 2.57139e-06
TNFRSF11B [NCBI] 2.42484e-06
SHH [NCBI] 1.69528e-06
RP [NCBI] 1.66371e-06
PWS [NCBI] 1.46838e-06
PTH [NCBI] 1.26877e-06
BDNF [NCBI] 1.16706e-06
MG [NCBI] 1.05917e-06
AS [NCBI] 7.22878e-07
ACHE [NCBI] 6.68153e-07
PCNA [NCBI] 3.25856e-07
EPO [NCBI] 2.94074e-07
CAT [NCBI] 8.79931e-08
panencephalitis, subacute sclerosing [NCBI] 6.83249e-08
MPO [NCBI] 3.44375e-09




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