|
OMIM |
Link |
Information gain |
01 |
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.000880362
|
|
|
restless legs syndrome, susceptibility to, 1
|
[NCBI]
|
0.000685
|
|
|
SLE
|
[NCBI]
|
0.000129315
|
|
|
TPO
|
[NCBI]
|
8.8496e-05
|
|
|
factor v deficiency
|
[NCBI]
|
7.72982e-05
|
|
|
PRL
|
[NCBI]
|
6.82416e-05
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
6.67504e-05
|
|
|
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to
|
[NCBI]
|
6.58021e-05
|
|
|
TG
|
[NCBI]
|
5.21076e-05
|
|
|
galactosemia
|
[NCBI]
|
4.81951e-05
|
|
|
CMT1B
|
[NCBI]
|
4.70281e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
4.62069e-05
|
|
|
CLS
|
[NCBI]
|
4.4928e-05
|
|
|
FGG
|
[NCBI]
|
4.36596e-05
|
|
|
factor x deficiency
|
[NCBI]
|
3.71474e-05
|
|
|
PCI
|
[NCBI]
|
3.62808e-05
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
3.39018e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
3.32733e-05
|
|
|
SLPI
|
[NCBI]
|
3.03996e-05
|
|
|
PCD
|
[NCBI]
|
2.98783e-05
|
|
|
PLTP
|
[NCBI]
|
2.88397e-05
|
|
|
LAM
|
[NCBI]
|
2.84283e-05
|
|
|
CRH
|
[NCBI]
|
2.13839e-05
|
|
|
LCAT
|
[NCBI]
|
2.08611e-05
|
|
|
AVP
|
[NCBI]
|
1.81869e-05
|
|
|
HP
|
[NCBI]
|
1.80509e-05
|
|
|
TFPI
|
[NCBI]
|
1.57896e-05
|
|
|
RA
|
[NCBI]
|
1.28552e-05
|
|
|
FMF
|
[NCBI]
|
1.13225e-05
|
|
|
CD
|
[NCBI]
|
1.05023e-05
|
|
|
F3
|
[NCBI]
|
7.76044e-06
|
|
|
TNF
|
[NCBI]
|
7.11949e-06
|
|
|
LPL
|
[NCBI]
|
6.50008e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
4.09581e-06
|
|
|
MG
|
[NCBI]
|
2.12166e-06
|
|
|
PTH
|
[NCBI]
|
2.46085e-07
|
|