Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Agranulocytosis	[NCBI]

Gene	Link	Information Gain
MPO	[NCBI]	5.3363e-05
MS	[NCBI]	5.28348e-05
TPMT	[NCBI]	1.96113e-05
NAT2	[NCBI]	1.35196e-05
NQO2	[NCBI]	1.16779e-05
MYOM2	[NCBI]	9.31504e-06
ELA2	[NCBI]	9.10424e-06
CD177	[NCBI]	8.51159e-06
TNF	[NCBI]	8.19693e-06
FCGR3B	[NCBI]	7.99667e-06
FCGR3A	[NCBI]	7.73612e-06
MSLN	[NCBI]	7.43398e-06
FCGR2A	[NCBI]	7.43398e-06
CYP2D6	[NCBI]	7.14126e-06
CYBA	[NCBI]	6.82343e-06
BTK	[NCBI]	6.01278e-06
HLA-A	[NCBI]	5.9945e-06
PIH	[NCBI]	5.82594e-06
HLA-B	[NCBI]	5.5851e-06
TROVE2	[NCBI]	5.38096e-06
HLA-DRB1	[NCBI]	4.17761e-06
AFP	[NCBI]	2.91141e-06

OMIM	Link	Information gain
neutropenia, chronic familial	[NCBI]	0.00852051
onychotrichodysplasia and neutropenia	[NCBI]	0.00162737
reticular dysgenesia	[NCBI]	0.00146324
cyclic hematopoiesis	[NCBI]	0.000808874
SCN1	[NCBI]	0.000619824
SDS	[NCBI]	0.000510938
whim syndrome	[NCBI]	0.000394958
COH1	[NCBI]	0.000341047
ATD1	[NCBI]	0.000314772
SCN3	[NCBI]	0.000249516
LAG5	[NCBI]	0.000229527
lazy leukocyte syndrome	[NCBI]	0.000190755
MPO	[NCBI]	0.000185724
eosinophilopenia	[NCBI]	0.000117708
combined inflammatory and immunologic defect	[NCBI]	0.000117708
granulocytopenia with immunoglobulin abnormality	[NCBI]	0.000117708
neutropenia, lethal congenital, with eosinophilia	[NCBI]	0.000117708
immunoerythromyeloid hypoplasia	[NCBI]	0.000117708
TPMT	[NCBI]	9.22713e-05
neutrophil-specific antigen: ne1	[NCBI]	8.71994e-05
carbimazole sensitivity	[NCBI]	8.12791e-05
neutrophil-specific antigen 1	[NCBI]	6.48439e-05
CHS	[NCBI]	5.61662e-05
CSF3R	[NCBI]	5.60027e-05
AP3B1	[NCBI]	5.21719e-05
ELA2	[NCBI]	5.06988e-05
thrombocytopenic purpura, autoimmune	[NCBI]	5.0139e-05
GCE	[NCBI]	4.80788e-05
BTHS	[NCBI]	4.08253e-05
CHH	[NCBI]	3.3086e-05
DBA	[NCBI]	2.50562e-05
hla-d histocompatibility type	[NCBI]	2.43067e-05
SLE	[NCBI]	1.83955e-05
HBB	[NCBI]	1.44322e-05
TNF	[NCBI]	1.21779e-05
AT	[NCBI]	1.12392e-05
RA	[NCBI]	9.09173e-06
AFP	[NCBI]	3.71442e-06