|
OMIM |
Link |
Information gain |
01 |
|
thyroid hormonogenesis, genetic defect in, 3
|
[NCBI]
|
0.0020498
|
|
|
lymphangiectasia, intestinal
|
[NCBI]
|
0.00192174
|
|
|
thyroid hormonogenesis, genetic defect in, 4
|
[NCBI]
|
0.00182656
|
|
|
thyroid hormonogenesis, genetic defect in, 5
|
[NCBI]
|
0.000618143
|
|
|
GRTH
|
[NCBI]
|
0.000261112
|
|
|
thyroid hormonogenesis, genetic defect in, 2a
|
[NCBI]
|
0.000219328
|
|
|
PDS
|
[NCBI]
|
0.000189
|
|
|
complement factor i deficiency
|
[NCBI]
|
0.000112764
|
|
|
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant
|
[NCBI]
|
0.000102248
|
|
|
pituitary dwarfism i
|
[NCBI]
|
9.63599e-05
|
|
|
CHNG1
|
[NCBI]
|
9.51001e-05
|
|
|
LHCGR
|
[NCBI]
|
8.30706e-05
|
|
|
HAE
|
[NCBI]
|
7.11382e-05
|
|
|
SLC6A4
|
[NCBI]
|
5.23714e-05
|
|
|
C3
|
[NCBI]
|
5.004e-05
|
|
|
AIS
|
[NCBI]
|
4.71077e-05
|
|
|
THRA
|
[NCBI]
|
2.55964e-05
|
|
|
IGKC
|
[NCBI]
|
2.43454e-05
|
|
|
SLC6A3
|
[NCBI]
|
2.17556e-05
|
|
|
TBG
|
[NCBI]
|
2.13754e-05
|
|
|
CFB
|
[NCBI]
|
2.12852e-05
|
|
|
F2
|
[NCBI]
|
2.10237e-05
|
|
|
NMU
|
[NCBI]
|
2.0235e-05
|
|
|
THRB
|
[NCBI]
|
1.99499e-05
|
|
|
BTK
|
[NCBI]
|
1.95493e-05
|
|
|
NGFB
|
[NCBI]
|
1.93513e-05
|
|
|
MECP2
|
[NCBI]
|
1.6372e-05
|
|
|
LRP1
|
[NCBI]
|
1.1939e-05
|
|
|
RA
|
[NCBI]
|
1.07934e-05
|
|
|
MB
|
[NCBI]
|
9.77544e-06
|
|
|
HP
|
[NCBI]
|
9.71073e-06
|
|
|
BDNF
|
[NCBI]
|
9.56908e-06
|
|
|
TF
|
[NCBI]
|
7.07767e-06
|
|
|
AVP
|
[NCBI]
|
7.0427e-06
|
|
|
GDNF
|
[NCBI]
|
6.57693e-06
|
|
|
MPO
|
[NCBI]
|
2.10418e-06
|
|
|
VIP
|
[NCBI]
|
1.64025e-06
|
|
|
KLK3
|
[NCBI]
|
1.10622e-06
|
|
|
CEACAM5
|
[NCBI]
|
9.59576e-07
|
|
|
SLE
|
[NCBI]
|
5.55262e-07
|
|
|
PTH
|
[NCBI]
|
3.11098e-07
|
|