Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hemagglutination [NCBI]

Gene


 Gene Link Information
Gain		 01
UMOD [NCBI] 1.59516e-05
VWF [NCBI] 1.34894e-05
GYPB [NCBI] 6.69789e-06
HTN3 [NCBI] 5.52344e-06
CD46 [NCBI] 4.12594e-06
C1GALT1C1 [NCBI] 3.43522e-06
PLDN [NCBI] 3.20277e-06
HTN1 [NCBI] 3.12833e-06
CFP [NCBI] 2.99533e-06
MPO [NCBI] 2.82925e-06
GYPA [NCBI] 2.67064e-06
XYLB [NCBI] 2.66442e-06
C4B [NCBI] 2.61191e-06
NAGA [NCBI] 2.60102e-06
CAMP [NCBI] 2.58517e-06
STATH [NCBI] 2.54541e-06
RHCE [NCBI] 2.52222e-06
CR1 [NCBI] 2.52222e-06
DARC [NCBI] 2.48742e-06
APOH [NCBI] 2.4286e-06
LGALS1 [NCBI] 2.42493e-06
REG1A [NCBI] 2.35727e-06
C3 [NCBI] 2.27163e-06
CFH [NCBI] 2.10942e-06
CA9 [NCBI] 2.10401e-06
EPB41L1 [NCBI] 1.87517e-06
CLU [NCBI] 1.86766e-06
WAS [NCBI] 1.84995e-06
EPB41L2 [NCBI] 1.83586e-06
TFRC [NCBI] 1.83586e-06
PF4 [NCBI] 1.79068e-06
TG [NCBI] 1.53462e-06
CD86 [NCBI] 1.5306e-06
CXCL12 [NCBI] 1.33959e-06
MBP [NCBI] 1.12924e-06
PTH [NCBI] 8.22156e-07
EGF [NCBI] 4.88331e-07



OMIM


 OMIM Link Information
gain		 01
blood group, p system [NCBI] 0.000222106
globulin anomaly involving beta (2a)-globulin [NCBI] 0.000171939
immune deficiency, familial variable [NCBI] 0.000144169
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive [NCBI] 9.24643e-05
B3GALNT1 [NCBI] 8.89116e-05
MBL2 [NCBI] 4.11591e-05
WAS [NCBI] 4.0825e-05
LAG5 [NCBI] 3.96604e-05
SLE [NCBI] 3.7519e-05
HS [NCBI] 2.72454e-05
CLU [NCBI] 2.42888e-05
HLA-A [NCBI] 2.39565e-05
MPO [NCBI] 1.86702e-05
SDC2 [NCBI] 1.81252e-05
PF4 [NCBI] 1.43851e-05
CYP1A1 [NCBI] 1.37819e-05
APOB [NCBI] 1.06721e-05
TG [NCBI] 9.78467e-06
MBP [NCBI] 5.9138e-06
RA [NCBI] 4.58993e-06
AVP [NCBI] 3.78626e-06
PTH [NCBI] 2.53883e-06
EGF [NCBI] 2.24566e-07
CF [NCBI] 9.19884e-08



Database Center for Life Science