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01 Histiocytes [NCBI]


Gene


Gene Link Information
Gain
01
CD68 [NCBI] 0.000473752
PIP [NCBI] 2.05244e-05
APOD [NCBI] 1.82425e-05
RPL22 [NCBI] 9.58072e-06
CD163 [NCBI] 8.02334e-06
TIA1 [NCBI] 7.97598e-06
SNRNP35 [NCBI] 7.51487e-06
ALK [NCBI] 7.08713e-06
SPN [NCBI] 6.85558e-06
ARMET [NCBI] 6.17236e-06
HYAL1 [NCBI] 5.50539e-06
TNF [NCBI] 5.14471e-06
PDPN [NCBI] 5.03897e-06
FCGRT [NCBI] 4.94223e-06
SERPINH1 [NCBI] 4.94223e-06
ST6GAL1 [NCBI] 4.58466e-06
FBLN5 [NCBI] 4.58466e-06
MUC5AC [NCBI] 4.1284e-06
CLC [NCBI] 4.0629e-06
ACVRL1 [NCBI] 3.94365e-06
TYR [NCBI] 3.86799e-06
CXCL13 [NCBI] 3.85764e-06
CD70 [NCBI] 3.64545e-06
CD14 [NCBI] 3.52093e-06
TGM2 [NCBI] 3.41047e-06
IGFBP1 [NCBI] 3.37207e-06
IRF4 [NCBI] 3.34728e-06
CCL22 [NCBI] 3.30536e-06
CD79A [NCBI] 3.28793e-06
BCL6 [NCBI] 3.25399e-06
MITF [NCBI] 2.9033e-06
AR [NCBI] 2.85101e-06
PAEP [NCBI] 2.82176e-06
PCNA [NCBI] 2.6338e-06
JUN [NCBI] 2.60923e-06
FASLG [NCBI] 2.55182e-06
MUC2 [NCBI] 2.54868e-06
MUC1 [NCBI] 2.52499e-06
NKX2-1 [NCBI] 2.37404e-06
MMP9 [NCBI] 2.31199e-06
PTHLH [NCBI] 1.89925e-06
ACP5 [NCBI] 1.64345e-06
ADA [NCBI] 1.60139e-06
PLAUR [NCBI] 1.42995e-06
HIF1A [NCBI] 1.128e-06
VEGFA [NCBI] 8.46757e-07
HGF [NCBI] 8.3953e-07
PTGS2 [NCBI] 5.37258e-07




OMIM


OMIM Link Information
gain
01
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 0.00567286
behcet syndrome [NCBI] 0.00152527
sea-blue histiocyte disease [NCBI] 0.00141944
histiocytosis with joint contractures and sensorineural deafness [NCBI] 0.00112909
panbronchiolitis, diffuse [NCBI] 0.000936179
NPC1 [NCBI] 0.000610628
CDAN2 [NCBI] 0.000567166
cardiomyopathy, infantile histiocytoid [NCBI] 0.000463633
niemann-pick disease, type b [NCBI] 0.000347054
neutrophilia, hereditary [NCBI] 0.000193274
histiocytic dermatoarthritis [NCBI] 0.000193274
cardiac lipidosis, familial [NCBI] 0.000193274
histiocytosis, progressive mucinous [NCBI] 0.000193274
gm1-gangliosidosis, type i [NCBI] 0.000190299
ceroid storage disease [NCBI] 0.000154028
hyaluronidase deficiency [NCBI] 0.000154028
hyaluronan metabolism, defect in [NCBI] 0.000154028
gaucher disease, type i [NCBI] 0.000148386
CGD [NCBI] 0.000131012
thrombocytopenic purpura, autoimmune [NCBI] 0.000125576
TGD [NCBI] 8.13673e-05
HFTC [NCBI] 8.13673e-05
mucopolysaccharidosis type vi [NCBI] 7.86617e-05
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i [NCBI] 7.28899e-05
sandhoff disease [NCBI] 6.48808e-05
CLN3 [NCBI] 6.41243e-05
RA [NCBI] 6.13814e-05
neuraminidase deficiency [NCBI] 5.53544e-05
mucolipidosis ii [NCBI] 5.28327e-05
HYAL1 [NCBI] 4.81194e-05
DBA [NCBI] 4.57832e-05
GALNT3 [NCBI] 4.36465e-05
BMP5 [NCBI] 4.36465e-05
AACT [NCBI] 4.01921e-05
ZS [NCBI] 3.73893e-05
FUS [NCBI] 3.61187e-05
DFSP [NCBI] 3.59305e-05
CYBB [NCBI] 3.32718e-05
fucosidosis [NCBI] 3.2768e-05
TNFRSF6 [NCBI] 3.22974e-05
MTCYB [NCBI] 3.20733e-05
wolman disease [NCBI] 3.01506e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 3.01506e-05
TYR [NCBI] 2.77432e-05
TNF [NCBI] 2.69607e-05
CCL22 [NCBI] 2.4911e-05
CHS [NCBI] 2.41603e-05
temporal arteritis [NCBI] 1.90098e-05
AT [NCBI] 1.76808e-05
PCNA [NCBI] 1.34579e-05
ALD [NCBI] 1.18252e-05
ACP5 [NCBI] 1.16676e-05
SPP1 [NCBI] 9.24655e-06
ADA [NCBI] 8.4073e-06
TNFSF6 [NCBI] 6.62932e-06
KLK3 [NCBI] 5.74078e-06
HGF [NCBI] 3.6556e-06
SLE [NCBI] 3.69775e-08
VEGF [NCBI] 1.70262e-08




Database Center for Life Science