|
OMIM |
Link |
Information
gain |
01 |
|
|
HHS
|
[NCBI]
|
0.000789981
|
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.000720653
|
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.000624176
|
|
|
|
DKC
|
[NCBI]
|
0.000433337
|
|
|
|
myelocerebellar disorder
|
[NCBI]
|
0.00029783
|
|
|
|
TPMT
|
[NCBI]
|
0.000165373
|
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
0.000153622
|
|
|
|
SDS
|
[NCBI]
|
0.000139586
|
|
|
|
DKC1
|
[NCBI]
|
0.000119232
|
|
|
|
intrauterine growth retardation with increased mitomycin c sensitivity
|
[NCBI]
|
9.47367e-05
|
|
|
|
FA
|
[NCBI]
|
8.97313e-05
|
|
|
|
CAMT
|
[NCBI]
|
8.07696e-05
|
|
|
|
ARL11
|
[NCBI]
|
7.25879e-05
|
|
|
|
MIRN15A
|
[NCBI]
|
6.67002e-05
|
|
|
|
MIRN16-1
|
[NCBI]
|
6.46996e-05
|
|
|
|
thiopurine s-methyltransferase deficiency
|
[NCBI]
|
6.29927e-05
|
|
|
|
MPL
|
[NCBI]
|
5.82665e-05
|
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
5.57321e-05
|
|
|
|
seckel syndrome 1
|
[NCBI]
|
5.47896e-05
|
|
|
|
JBS
|
[NCBI]
|
5.39002e-05
|
|
|
|
TERC
|
[NCBI]
|
5.06988e-05
|
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
5.06988e-05
|
|
|
|
PRF1
|
[NCBI]
|
5.06988e-05
|
|
|
|
HIDS
|
[NCBI]
|
5.00797e-05
|
|
|
|
SLE
|
[NCBI]
|
4.97341e-05
|
|
|
|
IVA
|
[NCBI]
|
4.81669e-05
|
|
|
|
CLL
|
[NCBI]
|
4.35316e-05
|
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
4.3093e-05
|
|
|
|
HS
|
[NCBI]
|
4.02693e-05
|
|
|
|
ARPKD
|
[NCBI]
|
3.5181e-05
|
|
|
|
JMML
|
[NCBI]
|
2.88364e-05
|
|
|
|
KSS
|
[NCBI]
|
2.12679e-05
|
|
|
|
WBS
|
[NCBI]
|
1.75319e-05
|
|
|
|
G6PD
|
[NCBI]
|
1.39258e-05
|
|
|
|
F3
|
[NCBI]
|
1.37745e-05
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
8.47578e-06
|
|
|
|
EPO
|
[NCBI]
|
7.03975e-06
|
|
|
|
MPO
|
[NCBI]
|
7.03632e-06
|
|
|
|
TNF
|
[NCBI]
|
5.65286e-07
|
|
|
|
RA
|
[NCBI]
|
5.30953e-07
|
|
