Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hemagglutination	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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