|
OMIM |
Link |
Information gain |
01 |
|
FA
|
[NCBI]
|
0.0441417
|
|
|
DBA
|
[NCBI]
|
0.00315719
|
|
|
FANCA
|
[NCBI]
|
0.00260314
|
|
|
FANCC
|
[NCBI]
|
0.00239062
|
|
|
diamond-blackfan anemia with microtia and cleft palate
|
[NCBI]
|
0.00119841
|
|
|
diamond-blackfan anemia 2
|
[NCBI]
|
0.00119841
|
|
|
XRCC9
|
[NCBI]
|
0.000971616
|
|
|
electroencephalogram, low-voltage
|
[NCBI]
|
0.000898321
|
|
|
transient erythroblastopenia of childhood
|
[NCBI]
|
0.000844965
|
|
|
FANCD2
|
[NCBI]
|
0.000767921
|
|
|
FANCE
|
[NCBI]
|
0.000686785
|
|
|
FANCB
|
[NCBI]
|
0.000650965
|
|
|
PCD
|
[NCBI]
|
0.000516429
|
|
|
FANCD1
|
[NCBI]
|
0.000362932
|
|
|
FANCF
|
[NCBI]
|
0.000342536
|
|
|
FANCM
|
[NCBI]
|
0.000342536
|
|
|
fanconi anemia, complementation group j
|
[NCBI]
|
0.000325263
|
|
|
PHF9
|
[NCBI]
|
0.000315673
|
|
|
FANCB
|
[NCBI]
|
0.000300926
|
|
|
BRCA2
|
[NCBI]
|
0.000298094
|
|
|
BRIP1
|
[NCBI]
|
0.000273682
|
|
|
RPS19
|
[NCBI]
|
0.000230885
|
|
|
FANCI
|
[NCBI]
|
0.000207551
|
|
|
fanconi anemia, complementation group n
|
[NCBI]
|
0.000162577
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
0.00015865
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
0.000151688
|
|
|
BGS
|
[NCBI]
|
0.000149338
|
|
|
PALB2
|
[NCBI]
|
0.000103392
|
|
|
RAD51
|
[NCBI]
|
9.21535e-05
|
|
|
KITLG
|
[NCBI]
|
8.65084e-05
|
|
|
anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome
|
[NCBI]
|
8.1275e-05
|
|
|
BRCA1
|
[NCBI]
|
8.01855e-05
|
|
|
PSPHL
|
[NCBI]
|
6.83731e-05
|
|
|
SNX5
|
[NCBI]
|
6.83731e-05
|
|
|
ZFP276
|
[NCBI]
|
6.83731e-05
|
|
|
UBE2T
|
[NCBI]
|
6.83731e-05
|
|
|
ZBTB32
|
[NCBI]
|
6.83731e-05
|
|
|
PARP1
|
[NCBI]
|
6.47413e-05
|
|
|
ZNF145
|
[NCBI]
|
6.33893e-05
|
|
|
NSX
|
[NCBI]
|
5.89103e-05
|
|
|
craniosynostosis-microcephaly with chromosomal breakage and other abnormalities
|
[NCBI]
|
5.89103e-05
|
|
|
C17ORF70
|
[NCBI]
|
5.46025e-05
|
|
|
PRKR
|
[NCBI]
|
5.46025e-05
|
|
|
FANCI
|
[NCBI]
|
5.46025e-05
|
|
|
VEGF
|
[NCBI]
|
4.99961e-05
|
|
|
OXTR
|
[NCBI]
|
4.94113e-05
|
|
|
DCLRE1A
|
[NCBI]
|
4.94113e-05
|
|
|
MX1
|
[NCBI]
|
4.94113e-05
|
|
|
KCNN4
|
[NCBI]
|
4.94113e-05
|
|
|
BLM
|
[NCBI]
|
4.6925e-05
|
|
|
FBP1
|
[NCBI]
|
4.60437e-05
|
|
|
EPO
|
[NCBI]
|
4.27618e-05
|
|
|
TNF
|
[NCBI]
|
4.21663e-05
|
|
|
myelocerebellar disorder
|
[NCBI]
|
4.11479e-05
|
|
|
aplastic anemia
|
[NCBI]
|
3.53854e-05
|
|
|
vater association
|
[NCBI]
|
2.80334e-05
|
|
|
TERC
|
[NCBI]
|
2.77073e-05
|
|
|
RECQL3
|
[NCBI]
|
2.61213e-05
|
|
|
ETV6
|
[NCBI]
|
2.61213e-05
|
|
|
NBS1
|
[NCBI]
|
2.57633e-05
|
|
|
medulloblastoma
|
[NCBI]
|
2.42811e-05
|
|
|
XPA
|
[NCBI]
|
2.38625e-05
|
|
|
BDC
|
[NCBI]
|
2.32303e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
2.1351e-05
|
|
|
seckel syndrome 1
|
[NCBI]
|
2.05049e-05
|
|
|
WAS
|
[NCBI]
|
1.9956e-05
|
|
|
EBN1
|
[NCBI]
|
1.82635e-05
|
|
|
HBA2
|
[NCBI]
|
1.55146e-05
|
|
|
NPM1
|
[NCBI]
|
1.43685e-05
|
|
|
ATM
|
[NCBI]
|
1.2946e-05
|
|
|
DHFR
|
[NCBI]
|
1.22861e-05
|
|
|
DKC
|
[NCBI]
|
9.68303e-06
|
|
|
XPA
|
[NCBI]
|
8.29112e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
7.32702e-06
|
|
|
PCNA
|
[NCBI]
|
7.29135e-06
|
|
|
TNFSF10
|
[NCBI]
|
6.97216e-06
|
|
|
RB1
|
[NCBI]
|
6.769e-06
|
|
|
CSA
|
[NCBI]
|
6.47557e-06
|
|
|
AFP
|
[NCBI]
|
5.35095e-06
|
|
|
WAS
|
[NCBI]
|
5.30778e-06
|
|
|
glioma of brain, familial
|
[NCBI]
|
4.8833e-06
|
|
|
WRN
|
[NCBI]
|
2.76445e-06
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
1.82779e-06
|
|
|
WT1
|
[NCBI]
|
1.30491e-06
|
|
|
MODY
|
[NCBI]
|
1.21567e-06
|
|
|
AT
|
[NCBI]
|
1.46421e-07
|
|
|
BCNS
|
[NCBI]
|
1.41616e-07
|
|
|
TNFSF6
|
[NCBI]
|
1.84417e-08
|
|
|
G6PD
|
[NCBI]
|
5.51776e-09
|
|