|
OMIM |
Link |
Information gain |
01 |
|
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
|
|