|
OMIM |
Link |
Information gain |
01 |
|
FA
|
[NCBI]
|
0.00577835
|
|
|
transient erythroblastopenia of childhood
|
[NCBI]
|
0.00182258
|
|
|
DBA
|
[NCBI]
|
0.00177066
|
|
|
EPO
|
[NCBI]
|
0.00126236
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.00117822
|
|
|
thrombocytopenia, autosomal recessive
|
[NCBI]
|
0.000724991
|
|
|
CDAN3
|
[NCBI]
|
0.000644828
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.00059657
|
|
|
kyphomelic dysplasia
|
[NCBI]
|
0.00059223
|
|
|
aplastic anemia
|
[NCBI]
|
0.000538237
|
|
|
CDAN2
|
[NCBI]
|
0.000488197
|
|
|
DKC
|
[NCBI]
|
0.000383049
|
|
|
FANCB
|
[NCBI]
|
0.000299794
|
|
|
chloramphenicol toxicity
|
[NCBI]
|
0.000292034
|
|
|
RA
|
[NCBI]
|
0.000274438
|
|
|
revesz syndrome
|
[NCBI]
|
0.000194616
|
|
|
TERC
|
[NCBI]
|
0.000174193
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
0.000150033
|
|
|
HS
|
[NCBI]
|
0.000130818
|
|
|
SDS
|
[NCBI]
|
0.000126971
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
0.000113817
|
|
|
PIGA
|
[NCBI]
|
0.000108141
|
|
|
chromosome 5q deletion syndrome
|
[NCBI]
|
0.00010202
|
|
|
fanconi-like syndrome
|
[NCBI]
|
9.7271e-05
|
|
|
CHH
|
[NCBI]
|
9.26195e-05
|
|
|
SLE
|
[NCBI]
|
9.0439e-05
|
|
|
BLM
|
[NCBI]
|
9.00944e-05
|
|
|
DKC1
|
[NCBI]
|
7.52052e-05
|
|
|
metaphyseal dysplasia without hypotrichosis
|
[NCBI]
|
7.48385e-05
|
|
|
PRF1
|
[NCBI]
|
7.23145e-05
|
|
|
IL2
|
[NCBI]
|
7.19381e-05
|
|
|
GFI1B
|
[NCBI]
|
6.98007e-05
|
|
|
IS
|
[NCBI]
|
6.63964e-05
|
|
|
THPO
|
[NCBI]
|
6.55718e-05
|
|
|
GSR
|
[NCBI]
|
6.4346e-05
|
|
|
XPA
|
[NCBI]
|
6.36996e-05
|
|
|
thrombocytosis, benign familial microcytic
|
[NCBI]
|
6.09282e-05
|
|
|
dyskeratosis congenita, autosomal recessive
|
[NCBI]
|
6.09282e-05
|
|
|
myelocerebellar disorder
|
[NCBI]
|
5.68724e-05
|
|
|
feline leukemia virus subgroup c receptor
|
[NCBI]
|
5.60288e-05
|
|
|
FANCD1
|
[NCBI]
|
5.36484e-05
|
|
|
KITLG
|
[NCBI]
|
5.2375e-05
|
|
|
adenosine deaminase, elevated, hemolytic anemia due to
|
[NCBI]
|
4.86905e-05
|
|
|
BST1
|
[NCBI]
|
4.74672e-05
|
|
|
GSTT1
|
[NCBI]
|
4.74672e-05
|
|
|
TERT
|
[NCBI]
|
4.71505e-05
|
|
|
SBDS
|
[NCBI]
|
4.49643e-05
|
|
|
monosomy 7 of bone marrow
|
[NCBI]
|
4.49342e-05
|
|
|
erythroleukemia, familial
|
[NCBI]
|
4.49342e-05
|
|
|
PGP
|
[NCBI]
|
4.29715e-05
|
|
|
HHS
|
[NCBI]
|
3.93946e-05
|
|
|
BDC
|
[NCBI]
|
3.82758e-05
|
|
|
PRG4
|
[NCBI]
|
3.75647e-05
|
|
|
RMRP
|
[NCBI]
|
3.75647e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
3.62607e-05
|
|
|
INAD1
|
[NCBI]
|
3.53468e-05
|
|
|
GSTM1
|
[NCBI]
|
3.27484e-05
|
|
|
TNFSF6
|
[NCBI]
|
3.20403e-05
|
|
|
LIF
|
[NCBI]
|
3.15593e-05
|
|
|
GP1BA
|
[NCBI]
|
3.15593e-05
|
|
|
thrombocythemia, essential
|
[NCBI]
|
3.08077e-05
|
|
|
DNTT
|
[NCBI]
|
2.86813e-05
|
|
|
IFNG
|
[NCBI]
|
2.86813e-05
|
|
|
NBS1
|
[NCBI]
|
2.71539e-05
|
|
|
PARP1
|
[NCBI]
|
2.68076e-05
|
|
|
HBG1
|
[NCBI]
|
2.55373e-05
|
|
|
FANCA
|
[NCBI]
|
2.39061e-05
|
|
|
RBS
|
[NCBI]
|
2.3793e-05
|
|
|
XLP1
|
[NCBI]
|
2.3793e-05
|
|
|
MAOA
|
[NCBI]
|
2.16991e-05
|
|
|
CSA
|
[NCBI]
|
1.89405e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
1.79107e-05
|
|
|
VEGF
|
[NCBI]
|
1.43882e-05
|
|
|
BRCA2
|
[NCBI]
|
1.30709e-05
|
|
|
IFNA1
|
[NCBI]
|
1.27207e-05
|
|
|
PLG
|
[NCBI]
|
1.16957e-05
|
|
|
JMML
|
[NCBI]
|
1.15009e-05
|
|
|
CYP1A1
|
[NCBI]
|
8.9762e-06
|
|
|
MG
|
[NCBI]
|
8.93333e-06
|
|
|
ADA
|
[NCBI]
|
7.5314e-06
|
|
|
ABCC1
|
[NCBI]
|
6.57832e-06
|
|
|
TPO
|
[NCBI]
|
5.92102e-06
|
|
|
PRL
|
[NCBI]
|
5.44643e-06
|
|
|
PCNA
|
[NCBI]
|
4.77307e-06
|
|
|
PF4
|
[NCBI]
|
4.69204e-06
|
|
|
AFP
|
[NCBI]
|
3.5549e-06
|
|
|
HBB
|
[NCBI]
|
1.50864e-06
|
|
|
AVP
|
[NCBI]
|
1.18351e-06
|
|
|
TNF
|
[NCBI]
|
1.14826e-06
|
|
|
HGF
|
[NCBI]
|
5.48416e-07
|
|
|
AT
|
[NCBI]
|
3.03011e-07
|
|
|
TG
|
[NCBI]
|
2.02011e-08
|
|