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MeSH keywords -> Related genes, diseases (OMIM)


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01 Granulomatous Disease, Chronic [NCBI]


Gene


Gene Link Information
Gain
01
NCF1C [NCBI] 0.0019819
CYBB [NCBI] 0.00179239
NCF1B [NCBI] 0.00104641
CYBA [NCBI] 0.000324866
NCF2 [NCBI] 0.000156576
NCF1 [NCBI] 0.000125614
MPO [NCBI] 6.66383e-05
NCF4 [NCBI] 5.42432e-05
NOX1 [NCBI] 3.34226e-05
BPI [NCBI] 2.16264e-05
MS [NCBI] 2.06195e-05
MDS1 [NCBI] 1.69718e-05
PRDM16 [NCBI] 1.64434e-05
XK [NCBI] 1.54583e-05
NOD2 [NCBI] 1.39896e-05
DECR1 [NCBI] 1.15874e-05
SETBP1 [NCBI] 1.06894e-05
SPI1 [NCBI] 9.39425e-06
NOX3 [NCBI] 9.32781e-06
JAK3 [NCBI] 8.55062e-06
LYN [NCBI] 8.41429e-06
ZAP70 [NCBI] 8.24107e-06
NOX5 [NCBI] 7.55162e-06
CTSG [NCBI] 7.47103e-06
CEACAM8 [NCBI] 6.34171e-06
NOX4 [NCBI] 6.28854e-06
FGR [NCBI] 5.79346e-06
IFNGR1 [NCBI] 5.48691e-06
LTF [NCBI] 5.44315e-06
CD47 [NCBI] 5.32135e-06
INPPL1 [NCBI] 4.95419e-06
IL2RG [NCBI] 4.81883e-06
INPP5D [NCBI] 4.6938e-06
LMO2 [NCBI] 4.6938e-06
ADA [NCBI] 4.24531e-06
FCGR3B [NCBI] 4.1528e-06
MAP3K14 [NCBI] 4.08254e-06
G6PD [NCBI] 4.07126e-06
SH2D1A [NCBI] 3.93807e-06
CD40LG [NCBI] 3.78272e-06
RAC1 [NCBI] 3.73784e-06
NLRP3 [NCBI] 3.72682e-06
DNASE1 [NCBI] 3.08074e-06
TAP2 [NCBI] 2.96954e-06
SLC11A1 [NCBI] 2.51309e-06
NOS2 [NCBI] 2.37002e-06
ABCG2 [NCBI] 2.32151e-06
BTK [NCBI] 2.28369e-06
NFKB1 [NCBI] 1.84918e-06
FOXP3 [NCBI] 1.50188e-06
FASLG [NCBI] 1.49808e-06
MLL [NCBI] 1.4496e-06
CASP3 [NCBI] 8.24085e-07
CD68 [NCBI] 5.10359e-07
BAX [NCBI] 1.64264e-07
AR [NCBI] 1.44701e-07
TNF [NCBI] 1.00708e-07
PTH [NCBI] 2.22991e-08




OMIM


OMIM Link Information
gain
01
CGD [NCBI] 0.00699931
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i [NCBI] 0.00289313
CYBB [NCBI] 0.001928
granulomatous disease, chronic, autosomal recessive, cytochrome b-negative [NCBI] 0.000818687
NCF2 [NCBI] 0.00077045
NCF1 [NCBI] 0.000694979
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type ii [NCBI] 0.000651274
XK [NCBI] 0.000440642
CYBA [NCBI] 0.000354644
MPO [NCBI] 0.000267057
synovitis, granulomatous, with uveitis and cranial neuropathies [NCBI] 0.000196835
SGD [NCBI] 0.000126252
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 0.000101438
CVID [NCBI] 8.72352e-05
granulomatous disease with defect in neutrophil chemotaxis [NCBI] 8.57276e-05
IFNGR1 [NCBI] 8.42347e-05
NCF4 [NCBI] 7.26222e-05
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist [NCBI] 7.1778e-05
CF [NCBI] 5.6084e-05
SCN3 [NCBI] 5.40623e-05
TAP2 [NCBI] 5.36533e-05
INDO [NCBI] 4.7777e-05
SCN1 [NCBI] 4.42067e-05
CTSG [NCBI] 4.41241e-05
IL12RB1 [NCBI] 4.27058e-05
CHS [NCBI] 3.88086e-05
OPTB1 [NCBI] 3.87965e-05
RP3 [NCBI] 3.71791e-05
glycogen storage disease ixa [NCBI] 2.82886e-05
NOD2 [NCBI] 2.63959e-05
VEGF [NCBI] 2.6146e-05
RP2 [NCBI] 2.46157e-05
DMD [NCBI] 1.17145e-05
ADA [NCBI] 1.1418e-05
DMD [NCBI] 1.10809e-05
TNF [NCBI] 9.75087e-06
G6PD [NCBI] 8.51737e-06
PTH [NCBI] 6.5538e-06
XDH [NCBI] 5.62856e-06
SPP1 [NCBI] 2.94357e-06
thrombocytopenic purpura, autoimmune [NCBI] 1.79298e-06
RNASE3 [NCBI] 1.26433e-06
F3 [NCBI] 6.27206e-07
RP [NCBI] 1.64905e-07




Database Center for Life Science