|
OMIM |
Link |
Information gain |
01 |
|
CMTX3
|
[NCBI]
|
0.00116883
|
|
|
hypoadrenocorticism, familial
|
[NCBI]
|
0.00116883
|
|
|
PCOS1
|
[NCBI]
|
0.000656357
|
|
|
AMCBX1
|
[NCBI]
|
0.000166738
|
|
|
intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
|
[NCBI]
|
0.000166738
|
|
|
XMPMA
|
[NCBI]
|
0.000138969
|
|
|
scapuloperoneal myopathy, x-linked dominant
|
[NCBI]
|
0.000138969
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
0.000106384
|
|
|
NYS1
|
[NCBI]
|
0.000101651
|
|
|
NETH
|
[NCBI]
|
0.000101651
|
|
|
RENS1
|
[NCBI]
|
9.61635e-05
|
|
|
DYT3
|
[NCBI]
|
9.06179e-05
|
|
|
EFE
|
[NCBI]
|
8.35644e-05
|
|
|
AHC
|
[NCBI]
|
8.27341e-05
|
|
|
FDH
|
[NCBI]
|
8.27341e-05
|
|
|
FHL1
|
[NCBI]
|
8.13595e-05
|
|
|
MCOPS7
|
[NCBI]
|
7.90366e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
7.59232e-05
|
|
|
BTHS
|
[NCBI]
|
7.37442e-05
|
|
|
DM2
|
[NCBI]
|
7.13215e-05
|
|
|
FRMD7
|
[NCBI]
|
5.47353e-05
|
|
|
IP
|
[NCBI]
|
5.36807e-05
|
|
|
PORCN
|
[NCBI]
|
4.33758e-05
|
|
|
HCCS
|
[NCBI]
|
4.13548e-05
|
|
|
NDUFA1
|
[NCBI]
|
4.13548e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
4.01651e-05
|
|
|
RTT
|
[NCBI]
|
3.79179e-05
|
|
|
TBX22
|
[NCBI]
|
3.76592e-05
|
|
|
FANCB
|
[NCBI]
|
3.76592e-05
|
|
|
FSCN2
|
[NCBI]
|
3.68069e-05
|
|
|
NLGN3
|
[NCBI]
|
3.68069e-05
|
|
|
SUMO1
|
[NCBI]
|
3.28857e-05
|
|
|
PQBP1
|
[NCBI]
|
3.11255e-05
|
|
|
TAF1
|
[NCBI]
|
2.86681e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
2.80936e-05
|
|
|
IKBKG
|
[NCBI]
|
2.75701e-05
|
|
|
RS1
|
[NCBI]
|
2.69372e-05
|
|
|
FLNA
|
[NCBI]
|
2.50308e-05
|
|
|
FOXP3
|
[NCBI]
|
2.38539e-05
|
|
|
MTTL1
|
[NCBI]
|
2.27255e-05
|
|
|
FA
|
[NCBI]
|
2.25052e-05
|
|
|
LMNA
|
[NCBI]
|
2.12439e-05
|
|
|
MAOA
|
[NCBI]
|
2.06494e-05
|
|
|
FGFR1
|
[NCBI]
|
1.96599e-05
|
|
|
DNMT1
|
[NCBI]
|
1.80129e-05
|
|
|
G6PD
|
[NCBI]
|
7.08854e-06
|
|
|
AR
|
[NCBI]
|
3.57458e-06
|
|
|
TNF
|
[NCBI]
|
6.65204e-09
|
|