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MeSH keywords -> Related genes, diseases (OMIM)


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01 Histocompatibility [NCBI]

Gene


 Gene Link Information
Gain		 01
D6S207E [NCBI] 0.000189081
HLA-H [NCBI] 0.000134121
HLA-DRB1 [NCBI] 3.42125e-05
HLA-A [NCBI] 2.85981e-05
HLA-C [NCBI] 2.80685e-05
HLA-B [NCBI] 2.17031e-05
HLA-DQB1 [NCBI] 1.88747e-05
IL10 [NCBI] 1.79801e-05
MS [NCBI] 1.62998e-05
HLA-DQA1 [NCBI] 1.22226e-05
HLA-DPB1 [NCBI] 1.08808e-05
TNF [NCBI] 9.86883e-06
IL6 [NCBI] 9.39507e-06
HLA-DPA1 [NCBI] 9.3694e-06
HMHA1 [NCBI] 7.01017e-06
IL4 [NCBI] 6.2136e-06
IFNG [NCBI] 6.15183e-06
GEM [NCBI] 5.86236e-06
KIR2DS2 [NCBI] 5.84733e-06
FASLG [NCBI] 5.84e-06
KLRC1 [NCBI] 4.89437e-06
IL1RN [NCBI] 4.87258e-06
ICAM1 [NCBI] 4.0796e-06
FOXN2 [NCBI] 3.69984e-06
CFD [NCBI] 3.2908e-06
KIAA0020 [NCBI] 3.12347e-06
JARID1D [NCBI] 3.01963e-06
KRT2 [NCBI] 2.95084e-06
IL10RB [NCBI] 2.89111e-06
KIR2DS1 [NCBI] 2.82604e-06
GLG1 [NCBI] 2.72823e-06
IL1RAP [NCBI] 2.6818e-06
KIR2DL1 [NCBI] 2.5866e-06
MPO [NCBI] 2.5433e-06
KIR2DL2 [NCBI] 2.49606e-06
NAGA [NCBI] 2.45677e-06
KIR2DL3 [NCBI] 2.39177e-06
PECAM1 [NCBI] 2.28813e-06
FCGR3B [NCBI] 2.14617e-06
CD52 [NCBI] 2.1276e-06
TNFRSF1B [NCBI] 2.0579e-06
FCGR3A [NCBI] 2.04908e-06
FCGR2A [NCBI] 2.01745e-06
KLRD1 [NCBI] 2.0054e-06
GZMA [NCBI] 1.98033e-06
LTA [NCBI] 1.85085e-06
MBL2 [NCBI] 1.8131e-06
CD83 [NCBI] 1.74597e-06
CTLA4 [NCBI] 1.73173e-06
JAK3 [NCBI] 1.72851e-06
WAS [NCBI] 1.70657e-06
SELPLG [NCBI] 1.67509e-06
MLL [NCBI] 1.48473e-06
FOXP3 [NCBI] 1.46892e-06
IFNGR1 [NCBI] 1.44622e-06
CD86 [NCBI] 1.38834e-06
ADA [NCBI] 1.35529e-06
IL1B [NCBI] 1.34525e-06
VDR [NCBI] 1.13105e-06
AFP [NCBI] 1.05776e-06
TGFB1 [NCBI] 8.9809e-07
PRL [NCBI] 6.58606e-07



OMIM


 OMIM Link Information
gain		 01
immune defect due to absence of thymus [NCBI] 0.00111709
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 0.000777651
hla-d histocompatibility type [NCBI] 0.000534346
HLA-A [NCBI] 0.000239592
hodgkin lymphoma [NCBI] 0.000170919
SPDA1 [NCBI] 0.000162755
hla modifier [NCBI] 0.000153137
PSORS1 [NCBI] 0.000122251
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 0.000120707
JMML [NCBI] 0.000119711
mixed lymphocyte culture locus ii [NCBI] 0.000114899
DBA [NCBI] 0.000112552
FA [NCBI] 9.16361e-05
IS [NCBI] 9.03146e-05
dystrophia myotonica 1 [NCBI] 8.15168e-05
FRA16A [NCBI] 8.10864e-05
alkaptonuria [NCBI] 7.70929e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive [NCBI] 7.37736e-05
WAS [NCBI] 7.29983e-05
glycogen storage disease iii [NCBI] 7.09344e-05
SCIDX1 [NCBI] 5.74784e-05
menkes disease [NCBI] 4.96383e-05
CGD [NCBI] 4.64282e-05
IHG [NCBI] 3.84059e-05
KIR2DL2 [NCBI] 3.36873e-05
KIR2DL3 [NCBI] 3.36873e-05
CFD [NCBI] 2.98411e-05
KIR2DL1 [NCBI] 2.93009e-05
RA [NCBI] 2.82176e-05
JARID1D [NCBI] 2.75297e-05
FUT2 [NCBI] 2.6169e-05
complement component 8 deficiency, type i [NCBI] 2.53216e-05
HLA-DQB1 [NCBI] 2.53216e-05
HLA-DRB1 [NCBI] 2.45809e-05
TNFSF6 [NCBI] 2.42164e-05
CHM [NCBI] 2.41344e-05
complement component 2 deficiency [NCBI] 2.26261e-05
ICAM1 [NCBI] 2.24622e-05
C4B [NCBI] 2.1849e-05
C4A [NCBI] 2.10353e-05
CTSC [NCBI] 2.07875e-05
IFNG [NCBI] 2.07875e-05
CFB [NCBI] 2.02106e-05
ALD [NCBI] 2.01219e-05
JAK3 [NCBI] 1.89343e-05
IL10 [NCBI] 1.84286e-05
CD [NCBI] 1.18916e-05
MBL2 [NCBI] 9.69194e-06
HP [NCBI] 7.84943e-06
MPO [NCBI] 6.75235e-06
ADA [NCBI] 4.11883e-06
VDR [NCBI] 2.75387e-06
AFP [NCBI] 9.86356e-07
SLE [NCBI] 8.94633e-07
CRH [NCBI] 4.51749e-07
PRL [NCBI] 6.58156e-08
TNF [NCBI] 4.51882e-08



Database Center for Life Science