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01 Agammaglobulinemia [NCBI]

Gene


 Gene Link Information
Gain		 01
BTK [NCBI] 0.00303005
TEC [NCBI] 6.60702e-05
SH2D1A [NCBI] 6.5748e-05
PLEK [NCBI] 5.82719e-05
HNRNPH2 [NCBI] 3.48702e-05
CXCL12 [NCBI] 2.62369e-05
TIMM8A [NCBI] 2.42918e-05
LRRC8A [NCBI] 2.38144e-05
CD79A [NCBI] 2.37212e-05
PAX5 [NCBI] 2.31039e-05
ITK [NCBI] 2.21141e-05
IGLL1 [NCBI] 2.05373e-05
JAK3 [NCBI] 2.01388e-05
GLA [NCBI] 1.97315e-05
CXCR4 [NCBI] 1.87539e-05
ELF4 [NCBI] 1.75159e-05
TLR8 [NCBI] 1.63209e-05
WAS [NCBI] 1.61457e-05
CD19 [NCBI] 1.61251e-05
RAG2 [NCBI] 1.57691e-05
CD40LG [NCBI] 1.56621e-05
SH3BP5 [NCBI] 1.35436e-05
CD79B [NCBI] 1.2568e-05
SYK [NCBI] 1.21307e-05
RAG1 [NCBI] 1.06756e-05
CBL [NCBI] 9.78732e-06
RPL36A [NCBI] 9.68308e-06
GNG2 [NCBI] 9.24984e-06
TAF7 [NCBI] 8.90472e-06
CD38 [NCBI] 8.62846e-06
GNB1 [NCBI] 8.37233e-06
PLCG2 [NCBI] 8.37233e-06
SH2D1B [NCBI] 8.37233e-06
BLNK [NCBI] 7.96721e-06
CD83 [NCBI] 7.905e-06
LYN [NCBI] 7.59664e-06
CCR7 [NCBI] 7.14584e-06
ADA [NCBI] 7.10214e-06
IKBKE [NCBI] 6.67473e-06
ADRBK2 [NCBI] 6.65294e-06
HNRNPK [NCBI] 6.49435e-06
CHUK [NCBI] 6.34385e-06
IKBKB [NCBI] 6.32432e-06
ICOS [NCBI] 6.03366e-06
POU2AF1 [NCBI] 5.86927e-06
KHDRBS1 [NCBI] 5.81787e-06
IL7R [NCBI] 5.67251e-06
CD55 [NCBI] 5.62674e-06
PGK1 [NCBI] 5.62674e-06
IL9 [NCBI] 5.58219e-06
AIF1 [NCBI] 5.19211e-06
TNFRSF13C [NCBI] 4.9056e-06
TNFRSF13B [NCBI] 4.9056e-06
CXCR5 [NCBI] 4.68706e-06
PIK3R1 [NCBI] 4.49433e-06
IL2RG [NCBI] 4.4059e-06
IKBKG [NCBI] 4.22304e-06
TNFRSF11A [NCBI] 4.17465e-06
PVR [NCBI] 4.00768e-06
SERPING1 [NCBI] 3.87874e-06
FCGR3B [NCBI] 3.74523e-06
MAPK8 [NCBI] 3.66213e-06
CCL22 [NCBI] 3.62218e-06
TIA1 [NCBI] 3.47189e-06
FYN [NCBI] 3.37924e-06
SRC [NCBI] 3.31325e-06
ABL1 [NCBI] 3.15006e-06
SOCS1 [NCBI] 3.07463e-06
TLR9 [NCBI] 2.63959e-06
CYBA [NCBI] 2.63959e-06
ZAP70 [NCBI] 2.5925e-06
CYBB [NCBI] 2.43014e-06
IL6 [NCBI] 2.25273e-06
SLC11A1 [NCBI] 2.13416e-06
DMPK [NCBI] 2.07384e-06
XIAP [NCBI] 1.93622e-06
PRKCB [NCBI] 1.89606e-06
IL1RN [NCBI] 1.78353e-06
GZMB [NCBI] 1.75769e-06
CD86 [NCBI] 1.44775e-06
IFNGR1 [NCBI] 1.34152e-06
ACP5 [NCBI] 1.21154e-06
FOXP3 [NCBI] 1.16671e-06
TNFSF11 [NCBI] 9.29275e-07
TNFRSF11B [NCBI] 8.98981e-07
TNF [NCBI] 8.18508e-07
IL10 [NCBI] 6.73301e-07
BCL2L1 [NCBI] 4.17145e-07
CD68 [NCBI] 2.85083e-07
EGF [NCBI] 2.44324e-07
AR [NCBI] 3.02638e-08
FASLG [NCBI] 2.15577e-08
AFP [NCBI] 9.51556e-09



OMIM


 OMIM Link Information
gain		 01
BTK [NCBI] 0.00597127
CVID [NCBI] 0.00384818
immune defect due to absence of thymus [NCBI] 0.00306599
IGAD1 [NCBI] 0.00240094
reticular dysgenesia [NCBI] 0.00139805
AGMX2 [NCBI] 0.000993831
lymphangiectasia, intestinal [NCBI] 0.000694153
hypogammaglobulinemia and isolated growth hormone deficiency, x-linked [NCBI] 0.000614824
immunoglobulin m, level of [NCBI] 0.000601551
agammaglobulinemia, non-bruton type, autosomal recessive [NCBI] 0.000568315
spondyloepimetaphyseal dysplasia, sponastrime type [NCBI] 0.000502422
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive [NCBI] 0.00047786
XLP1 [NCBI] 0.000424257
SCIDX1 [NCBI] 0.000395581
dubowitz syndrome [NCBI] 0.000346579
achondroplasia, so-called, and severe combined immunodeficiency [NCBI] 0.000332072
whim syndrome [NCBI] 0.000332072
thrombocytopenia-absent radius syndrome [NCBI] 0.000307508
RA [NCBI] 0.000257614
proteus syndrome [NCBI] 0.000245608
BLNK [NCBI] 0.000170732
SH2D1A [NCBI] 0.000150926
LRRC8 [NCBI] 0.000141283
AT [NCBI] 0.000137973
HIGM1 [NCBI] 0.000137843
lymphoid system deterioration, progressive [NCBI] 0.000102219
hemosiderosis, pulmonary, with deficiency of gamma-a globulin [NCBI] 0.000102219
immunoerythromyeloid hypoplasia [NCBI] 0.000102219
diarrhea, glucose-stimulated secretory, with common variable immunodeficiency [NCBI] 0.000102219
granulomatous disease due to combined cellular and humoral immune defects [NCBI] 0.000102219
retinal telangiectasia and hypogammaglobulinemia [NCBI] 0.000102219
TIMM8A [NCBI] 8.95093e-05
CXCR4 [NCBI] 8.01932e-05
immunodeficiency, partial combined, with absence of hla determinants and beta-2-microglobulin from lymphocytes [NCBI] 7.97757e-05
immune deficiency, familial variable [NCBI] 7.97757e-05
transcobalamin ii deficiency [NCBI] 7.39043e-05
CD40LG [NCBI] 7.13855e-05
hypoproteinemia, hypercatabolic [NCBI] 7.1323e-05
HNRPH2 [NCBI] 7.05996e-05
SH3BP5 [NCBI] 7.05996e-05
thymoma, familial [NCBI] 6.58442e-05
microcephaly with chemotactic defect and transient hypogammaglobulinemia [NCBI] 6.58442e-05
immunodeficiency with hyper-igm, type 2 [NCBI] 6.17778e-05
anemia, autoimmune hemolytic [NCBI] 5.85433e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive [NCBI] 5.85433e-05
IGLL1 [NCBI] 5.6827e-05
FCGRT [NCBI] 5.16337e-05
CD19 [NCBI] 5.16337e-05
IGHM [NCBI] 4.8264e-05
WAS [NCBI] 4.24971e-05
cutis laxa, autosomal recessive, type ii [NCBI] 4.20234e-05
severe combined immunodeficiency with sensitivity to ionizing radiation [NCBI] 4.20234e-05
omenn syndrome [NCBI] 3.9243e-05
IL7R [NCBI] 3.83574e-05
AEZ [NCBI] 3.42468e-05
pulmonary fibrosis, idiopathic [NCBI] 3.25322e-05
LAD [NCBI] 3.09983e-05
immunodeficiency-centromeric instability-facial anomalies syndrome [NCBI] 3.00594e-05
complement component 2 deficiency [NCBI] 2.79343e-05
PGK1 [NCBI] 2.49324e-05
kartagener syndrome [NCBI] 2.39081e-05
bare lymphocyte syndrome, type ii [NCBI] 2.30612e-05
DMPK [NCBI] 2.28674e-05
RTS [NCBI] 2.25254e-05
ADA [NCBI] 2.17567e-05
B2M [NCBI] 2.10125e-05
IL10 [NCBI] 1.97614e-05
CHH [NCBI] 1.88918e-05
BLM [NCBI] 1.81276e-05
CD [NCBI] 1.48446e-05
EGF [NCBI] 1.29074e-05
hla-d histocompatibility type [NCBI] 9.11719e-06
DGS [NCBI] 7.04405e-06
thrombocytopenic purpura, autoimmune [NCBI] 6.98179e-06
SLE [NCBI] 6.46236e-06
MG [NCBI] 3.46202e-06
TNF [NCBI] 2.80158e-06
AFP [NCBI] 2.7421e-06
lymphoma, non-hodgkin, familial [NCBI] 1.26804e-06
AR [NCBI] 8.98378e-07



Database Center for Life Science