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01 Hypergammaglobulinemia [NCBI]

Gene


 Gene Link Information
Gain		 01
CD40LG [NCBI] 0.000161862
MVK [NCBI] 0.000113568
MS [NCBI] 0.000105673
AICDA [NCBI] 6.53977e-05
MEFV [NCBI] 4.98393e-05
BTK [NCBI] 3.99891e-05
CD40 [NCBI] 3.08616e-05
NLRP3 [NCBI] 3.00271e-05
IKBKG [NCBI] 2.38354e-05
TROVE2 [NCBI] 2.12826e-05
UNG [NCBI] 1.94643e-05
TRAF3 [NCBI] 1.79608e-05
MAG [NCBI] 1.69199e-05
MYOM2 [NCBI] 1.61233e-05
C12orf32 [NCBI] 1.30122e-05
TNFRSF1A [NCBI] 1.26866e-05
STAT6 [NCBI] 1.18586e-05
TNFSF13B [NCBI] 1.17325e-05
PSMG2 [NCBI] 1.15306e-05
TFRC [NCBI] 1.1302e-05
LAIR1 [NCBI] 1.07514e-05
SWAP70 [NCBI] 1.07514e-05
IKBKE [NCBI] 1.02571e-05
CHUK [NCBI] 9.9126e-06
IKBKB [NCBI] 9.89222e-06
CCNO [NCBI] 9.64043e-06
SH2D2A [NCBI] 9.48433e-06
IL25 [NCBI] 9.34128e-06
PSTPIP1 [NCBI] 9.20928e-06
IL1RN [NCBI] 9.18153e-06
SMUG1 [NCBI] 9.08674e-06
FAS [NCBI] 8.89302e-06
GFI1 [NCBI] 8.86522e-06
DLAT [NCBI] 8.57894e-06
XBP1 [NCBI] 8.33382e-06
REL [NCBI] 7.87015e-06
ICOS [NCBI] 7.87015e-06
TRAF2 [NCBI] 7.75794e-06
SBDS [NCBI] 7.16746e-06
TNFRSF13C [NCBI] 6.73019e-06
CD70 [NCBI] 6.35905e-06
PTX3 [NCBI] 6.03529e-06
IL12A [NCBI] 5.84962e-06
RAG2 [NCBI] 5.2022e-06
FAH [NCBI] 5.14367e-06
PIGA [NCBI] 4.94861e-06
JAK3 [NCBI] 4.49604e-06
ZAP70 [NCBI] 4.34096e-06
IL6ST [NCBI] 4.2653e-06
TNF [NCBI] 4.09448e-06
AMBP [NCBI] 3.97142e-06
TAP1 [NCBI] 3.88437e-06
HP [NCBI] 3.63516e-06
RAG1 [NCBI] 3.51353e-06
IL4 [NCBI] 3.27048e-06
CD86 [NCBI] 3.07965e-06
RUNX1 [NCBI] 3.01804e-06
CD38 [NCBI] 2.83379e-06
FOXP3 [NCBI] 2.7484e-06
STAT1 [NCBI] 2.73838e-06
LIF [NCBI] 2.6512e-06
TNFRSF11B [NCBI] 2.41768e-06
CALCA [NCBI] 2.04352e-06
CD68 [NCBI] 1.53553e-06
EPO [NCBI] 8.86078e-07
MPO [NCBI] 8.65263e-07
PRL [NCBI] 7.23626e-07



OMIM


 OMIM Link Information
gain		 01
HIGM1 [NCBI] 0.00230978
HIDS [NCBI] 0.00147341
storage pool platelet disease [NCBI] 0.00106493
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 0.000783229
CD40LG [NCBI] 0.000688631
MVK [NCBI] 0.000563218
MAG [NCBI] 0.000388559
periodic fever, familial, autosomal dominant [NCBI] 0.000297163
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist [NCBI] 0.000283562
FMF [NCBI] 0.000212328
hyperimmunoglobulin g1(a1) syndrome [NCBI] 0.000182272
immunodeficiency with hyper-igm, type 3 [NCBI] 0.000158722
immunodeficiency with hyper-igm, type 2 [NCBI] 0.000158722
immunodeficiency with hyper-igm, type 4 [NCBI] 0.000106537
combined inflammatory and immunologic defect [NCBI] 0.000106537
UNG [NCBI] 0.000103761
AICDA [NCBI] 0.000100134
LIP [NCBI] 8.45358e-05
splenomegaly syndrome with splenic germinal center hypoplasia and reduced circulating t-helper cells [NCBI] 8.40868e-05
IKBKG [NCBI] 8.33318e-05
TNFRSF6 [NCBI] 7.94938e-05
cirrhosis, familial [NCBI] 7.56273e-05
ALPS2A [NCBI] 7.56273e-05
RA [NCBI] 6.77093e-05
CF [NCBI] 6.72226e-05
calcific aortic disease with immunologic abnormalities, familial [NCBI] 6.60682e-05
SH2D2A [NCBI] 6.39235e-05
SLE [NCBI] 6.24238e-05
PBC [NCBI] 5.78337e-05
ectodermal dysplasia, hypohidrotic, with immune deficiency [NCBI] 5.78337e-05
IL25 [NCBI] 5.53521e-05
TNFRSF13C [NCBI] 5.53521e-05
ALPS [NCBI] 5.47023e-05
HHS [NCBI] 5.24412e-05
ICOSLG [NCBI] 5.08467e-05
TRAF2 [NCBI] 4.77651e-05
CD40 [NCBI] 4.65233e-05
myeloma, multiple [NCBI] 4.43148e-05
IPEX [NCBI] 4.18171e-05
glycogen storage disease ib [NCBI] 3.61196e-05
IGHG1 [NCBI] 3.60585e-05
BCGF [NCBI] 3.56018e-05
XLP1 [NCBI] 3.24105e-05
JAK3 [NCBI] 3.16207e-05
STAT6 [NCBI] 2.9365e-05
BCL2 [NCBI] 2.91661e-05
IL4 [NCBI] 2.75411e-05
AT [NCBI] 2.27081e-05
hla-d histocompatibility type [NCBI] 1.53309e-05
HP [NCBI] 1.18674e-05
CHS [NCBI] 8.92246e-06
TTR [NCBI] 6.80722e-06
lymphoma, non-hodgkin, familial [NCBI] 4.72733e-06
TNFSF6 [NCBI] 3.65783e-06
TNF [NCBI] 2.47408e-06
CEACAM5 [NCBI] 1.51923e-06
PRL [NCBI] 4.8319e-08
EPO [NCBI] 3.52741e-08
MPO [NCBI] 3.49119e-08



Database Center for Life Science