|
OMIM |
Link |
Information gain |
01 |
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.00103098
|
|
|
thrombocytopenia, autosomal recessive
|
[NCBI]
|
0.000959988
|
|
|
transient erythroblastopenia of childhood
|
[NCBI]
|
0.000860189
|
|
|
reticular dysgenesia
|
[NCBI]
|
0.000860189
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.000860189
|
|
|
r binder deficiency with lactoferrin deficiency
|
[NCBI]
|
0.000860189
|
|
|
EPO
|
[NCBI]
|
0.000737707
|
|
|
CDAN3
|
[NCBI]
|
0.000709234
|
|
|
neutropenia, chronic familial
|
[NCBI]
|
0.000650385
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000578365
|
|
|
CDAN2
|
[NCBI]
|
0.000491221
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000471124
|
|
|
HBFQTL2
|
[NCBI]
|
0.000421627
|
|
|
myeloproliferative syndrome, transient
|
[NCBI]
|
0.000421627
|
|
|
THC2
|
[NCBI]
|
0.000343978
|
|
|
DBA
|
[NCBI]
|
0.000309854
|
|
|
formiminotransferase deficiency
|
[NCBI]
|
0.000184598
|
|
|
hexokinase deficiency hemolytic anemia
|
[NCBI]
|
0.000156651
|
|
|
THC1
|
[NCBI]
|
0.000143953
|
|
|
erythrocytosis, familial, 1
|
[NCBI]
|
0.000140494
|
|
|
cyclic hematopoiesis
|
[NCBI]
|
0.000140494
|
|
|
autoimmune disease
|
[NCBI]
|
0.000140494
|
|
|
cardioauditory syndrome of sanchez cascos
|
[NCBI]
|
0.000125878
|
|
|
fibrinolytic defect
|
[NCBI]
|
0.000125878
|
|
|
CF
|
[NCBI]
|
0.000110708
|
|
|
CML
|
[NCBI]
|
0.000100698
|
|
|
thrombocytopenia, cyclic
|
[NCBI]
|
9.81409e-05
|
|
|
athrombia, essential
|
[NCBI]
|
9.81409e-05
|
|
|
glomerulonephritis with sparse hair and telangiectases
|
[NCBI]
|
9.81409e-05
|
|
|
TNF
|
[NCBI]
|
9.32274e-05
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
8.76951e-05
|
|
|
bernard-soulier syndrome, benign autosomal dominant
|
[NCBI]
|
8.76951e-05
|
|
|
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to
|
[NCBI]
|
8.09247e-05
|
|
|
paget disease, juvenile
|
[NCBI]
|
7.19031e-05
|
|
|
aplastic anemia
|
[NCBI]
|
6.85857e-05
|
|
|
caffey disease
|
[NCBI]
|
6.32775e-05
|
|
|
xx male syndrome
|
[NCBI]
|
6.32775e-05
|
|
|
IS
|
[NCBI]
|
6.32775e-05
|
|
|
epstein syndrome
|
[NCBI]
|
6.10842e-05
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
6.10842e-05
|
|
|
giant platelet syndrome
|
[NCBI]
|
6.02404e-05
|
|
|
ALPS
|
[NCBI]
|
5.94883e-05
|
|
|
erythrocytosis, familial, 2
|
[NCBI]
|
5.41886e-05
|
|
|
chromosome 5q deletion syndrome
|
[NCBI]
|
5.27937e-05
|
|
|
TTP
|
[NCBI]
|
5.14944e-05
|
|
|
PF4
|
[NCBI]
|
4.72035e-05
|
|
|
porphyria, congenital erythropoietic
|
[NCBI]
|
4.7043e-05
|
|
|
EL1
|
[NCBI]
|
4.7043e-05
|
|
|
BCR
|
[NCBI]
|
4.70242e-05
|
|
|
PPH1
|
[NCBI]
|
4.51611e-05
|
|
|
thrombocythemia, essential
|
[NCBI]
|
4.51611e-05
|
|
|
CHAC
|
[NCBI]
|
4.51611e-05
|
|
|
bartter syndrome, type 3
|
[NCBI]
|
4.42874e-05
|
|
|
HBB
|
[NCBI]
|
4.28879e-05
|
|
|
G6PD
|
[NCBI]
|
4.23579e-05
|
|
|
ALMS
|
[NCBI]
|
4.18915e-05
|
|
|
OPTB1
|
[NCBI]
|
4.1158e-05
|
|
|
SLE
|
[NCBI]
|
3.9532e-05
|
|
|
DKC
|
[NCBI]
|
3.91212e-05
|
|
|
ADA
|
[NCBI]
|
3.85762e-05
|
|
|
MPO
|
[NCBI]
|
3.78465e-05
|
|
|
FIH
|
[NCBI]
|
3.56356e-05
|
|
|
EGF
|
[NCBI]
|
3.53359e-05
|
|
|
aHUS
|
[NCBI]
|
3.46121e-05
|
|
|
RNASE3
|
[NCBI]
|
3.43724e-05
|
|
|
HS
|
[NCBI]
|
3.3337e-05
|
|
|
ABL1
|
[NCBI]
|
3.26852e-05
|
|
|
ARHGAP4
|
[NCBI]
|
3.05044e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
2.98693e-05
|
|
|
OCP
|
[NCBI]
|
2.94977e-05
|
|
|
maple syrup urine disease
|
[NCBI]
|
2.94977e-05
|
|
|
BCGF
|
[NCBI]
|
2.74295e-05
|
|
|
HPA-2
|
[NCBI]
|
2.69901e-05
|
|
|
homocystinuria
|
[NCBI]
|
2.62703e-05
|
|
|
LPI
|
[NCBI]
|
2.50304e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
2.42176e-05
|
|
|
glycogen storage disease ii
|
[NCBI]
|
2.42176e-05
|
|
|
CRC
|
[NCBI]
|
2.36644e-05
|
|
|
CLC
|
[NCBI]
|
2.32184e-05
|
|
|
SDS
|
[NCBI]
|
2.2952e-05
|
|
|
von willebrand disease
|
[NCBI]
|
2.29263e-05
|
|
|
CCD
|
[NCBI]
|
2.24739e-05
|
|
|
GSS
|
[NCBI]
|
2.19705e-05
|
|
|
XG
|
[NCBI]
|
2.04901e-05
|
|
|
HP
|
[NCBI]
|
2.00376e-05
|
|
|
ALB
|
[NCBI]
|
1.78094e-05
|
|
|
XK
|
[NCBI]
|
1.77625e-05
|
|
|
MPL
|
[NCBI]
|
1.74972e-05
|
|
|
MYH9
|
[NCBI]
|
1.67681e-05
|
|
|
TFPI
|
[NCBI]
|
1.64733e-05
|
|
|
AK1
|
[NCBI]
|
1.53615e-05
|
|
|
TERC
|
[NCBI]
|
1.51864e-05
|
|
|
CDKN1A
|
[NCBI]
|
1.50166e-05
|
|
|
anemia, sideroblastic, x-linked
|
[NCBI]
|
1.48518e-05
|
|
|
PIGA
|
[NCBI]
|
1.46918e-05
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
1.4094e-05
|
|
|
CSF2
|
[NCBI]
|
1.38176e-05
|
|
|
RUNX1
|
[NCBI]
|
1.33034e-05
|
|
|
GSR
|
[NCBI]
|
1.33034e-05
|
|
|
factor x deficiency
|
[NCBI]
|
1.30633e-05
|
|
|
F13A1
|
[NCBI]
|
1.25057e-05
|
|
|
A2M
|
[NCBI]
|
1.20976e-05
|
|
|
MMP9
|
[NCBI]
|
1.17184e-05
|
|
|
LCN2
|
[NCBI]
|
1.14507e-05
|
|
|
FMF
|
[NCBI]
|
1.09902e-05
|
|
|
FGA
|
[NCBI]
|
1.04984e-05
|
|
|
HRG
|
[NCBI]
|
1.00805e-05
|
|
|
LBP
|
[NCBI]
|
9.45213e-06
|
|
|
IFNA1
|
[NCBI]
|
8.34474e-06
|
|
|
MAPK1
|
[NCBI]
|
8.34474e-06
|
|
|
TPMT
|
[NCBI]
|
7.89469e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
7.45147e-06
|
|
|
FA
|
[NCBI]
|
6.77017e-06
|
|
|
EPOR
|
[NCBI]
|
5.41459e-06
|
|
|
MJD
|
[NCBI]
|
5.34777e-06
|
|
|
PRL
|
[NCBI]
|
4.7671e-06
|
|
|
GNRH1
|
[NCBI]
|
4.32203e-06
|
|
|
F3
|
[NCBI]
|
4.18789e-06
|
|
|
HBA1
|
[NCBI]
|
3.93292e-06
|
|
|
GPI
|
[NCBI]
|
3.41617e-06
|
|
|
CP
|
[NCBI]
|
3.21223e-06
|
|
|
RA
|
[NCBI]
|
2.77928e-06
|
|
|
TPO
|
[NCBI]
|
2.75042e-06
|
|
|
AR
|
[NCBI]
|
2.73205e-06
|
|
|
OSM
|
[NCBI]
|
2.6839e-06
|
|
|
GTS
|
[NCBI]
|
2.44664e-06
|
|
|
PTH
|
[NCBI]
|
2.42721e-06
|
|
|
temporal arteritis
|
[NCBI]
|
2.41991e-06
|
|
|
FGF7
|
[NCBI]
|
1.65934e-06
|
|
|
PCNA
|
[NCBI]
|
1.5046e-06
|
|
|
TLR4
|
[NCBI]
|
1.26071e-06
|
|
|
IL2
|
[NCBI]
|
1.24386e-06
|
|
|
HGF
|
[NCBI]
|
1.18767e-06
|
|
|
CAT
|
[NCBI]
|
9.97121e-07
|
|
|
CFTR
|
[NCBI]
|
9.84148e-07
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
8.66975e-07
|
|
|
NPPA
|
[NCBI]
|
6.63225e-07
|
|
|
XDH
|
[NCBI]
|
5.52781e-07
|
|
|
TF
|
[NCBI]
|
3.48363e-07
|
|
|
VEGF
|
[NCBI]
|
2.77312e-07
|
|
|
CEACAM5
|
[NCBI]
|
2.48202e-07
|
|
|
AHR
|
[NCBI]
|
1.33834e-07
|
|
|
ACHE
|
[NCBI]
|
1.50775e-08
|
|
|
TG
|
[NCBI]
|
1.26654e-08
|
|