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MeSH keywords -> Related genes, diseases (OMIM)


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01 Multicenter Studies as Topic [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
VRNI [NCBI] 0.000730759
HFM [NCBI] 0.000573785
MDD [NCBI] 0.000351255
RA [NCBI] 0.000240963
KLK3 [NCBI] 9.70222e-05
thrombocytopenic purpura, autoimmune [NCBI] 8.40082e-05
OPLL [NCBI] 7.47322e-05
stroke, ischemic [NCBI] 5.58602e-05
polycythemia vera [NCBI] 5.58602e-05
CRC [NCBI] 4.81293e-05
PCA3 [NCBI] 4.02008e-05
lymphoma, non-hodgkin, familial [NCBI] 3.83491e-05
CLS [NCBI] 3.75281e-05
ARPKD [NCBI] 3.71589e-05
GC [NCBI] 3.39591e-05
MIA [NCBI] 3.13774e-05
GNRH1 [NCBI] 2.85495e-05
hypercholesterolemia, autosomal dominant [NCBI] 2.44065e-05
AFP [NCBI] 2.34502e-05
GSTM1 [NCBI] 2.28266e-05
TNNT2 [NCBI] 2.26158e-05
GLI3 [NCBI] 2.18412e-05
PAI1 [NCBI] 2.09984e-05
LTA [NCBI] 2.08435e-05
MMP3 [NCBI] 2.01257e-05
IL10 [NCBI] 1.71363e-05
ACHE [NCBI] 1.4893e-05
TNF [NCBI] 1.48189e-05
PLTP [NCBI] 1.23855e-05
GJB2 [NCBI] 1.15621e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 1.13889e-05
BRCA1 [NCBI] 1.03838e-05
ACPP [NCBI] 9.91376e-06
PD [NCBI] 9.84144e-06
EPO [NCBI] 9.16726e-06
MBL2 [NCBI] 8.48971e-06
STAT3 [NCBI] 8.01574e-06
GHRH [NCBI] 7.59804e-06
temporal arteritis [NCBI] 7.22739e-06
polycystic kidneys [NCBI] 6.87245e-06
PF4 [NCBI] 6.70494e-06
HP [NCBI] 6.69401e-06
TLR4 [NCBI] 5.93397e-06
IL2 [NCBI] 5.90656e-06
hla-d histocompatibility type [NCBI] 5.66767e-06
TFPI [NCBI] 5.50747e-06
CF [NCBI] 5.25465e-06
COMT [NCBI] 4.85304e-06
SLC6A3 [NCBI] 4.31229e-06
APOB [NCBI] 3.55799e-06
CEACAM5 [NCBI] 3.48443e-06
SLE [NCBI] 2.25661e-06
AD [NCBI] 1.20624e-06
NGFB [NCBI] 8.30381e-07
PTH [NCBI] 8.2698e-07
MBP [NCBI] 5.01287e-07
MPO [NCBI] 3.60128e-07
APOE [NCBI] 3.58569e-07
APC [NCBI] 2.34294e-07
NPY [NCBI] 1.60978e-07
VEGF [NCBI] 1.00965e-07
PCNA [NCBI] 7.97924e-09




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