|
OMIM |
Link |
Information gain |
01 |
|
MACOM
|
[NCBI]
|
0.00279952
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.00126979
|
|
|
alacrima, congenital
|
[NCBI]
|
0.0010375
|
|
|
MGC1
|
[NCBI]
|
0.0010375
|
|
|
cornea guttata with anterior polar cataracts
|
[NCBI]
|
0.0010375
|
|
|
CND
|
[NCBI]
|
0.000737684
|
|
|
CNA1
|
[NCBI]
|
0.000684465
|
|
|
OCP
|
[NCBI]
|
0.000451295
|
|
|
KERA
|
[NCBI]
|
0.000376382
|
|
|
CNA2
|
[NCBI]
|
0.000285744
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000271087
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
0.000243839
|
|
|
corneal degeneration, band-shaped spheroid
|
[NCBI]
|
0.000204216
|
|
|
keratitis, hereditary
|
[NCBI]
|
0.000180644
|
|
|
ATS
|
[NCBI]
|
0.000177193
|
|
|
EGF
|
[NCBI]
|
0.000144483
|
|
|
KTCN1
|
[NCBI]
|
0.000128314
|
|
|
FED
|
[NCBI]
|
0.000123813
|
|
|
VRNI
|
[NCBI]
|
0.000118779
|
|
|
corneodermatoosseous syndrome
|
[NCBI]
|
0.000117451
|
|
|
corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation
|
[NCBI]
|
0.000117451
|
|
|
mucolipidosis iv
|
[NCBI]
|
0.000114221
|
|
|
AN2
|
[NCBI]
|
9.89341e-05
|
|
|
RDC
|
[NCBI]
|
9.49899e-05
|
|
|
SLE
|
[NCBI]
|
8.17179e-05
|
|
|
LOCS
|
[NCBI]
|
8.10223e-05
|
|
|
DSPG3
|
[NCBI]
|
8.01986e-05
|
|
|
corneal dystrophy and perceptive deafness
|
[NCBI]
|
7.69378e-05
|
|
|
PAX6
|
[NCBI]
|
7.39628e-05
|
|
|
foveal hypoplasia and presenile cataract syndrome
|
[NCBI]
|
7.09823e-05
|
|
|
NN
|
[NCBI]
|
7.09823e-05
|
|
|
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
|
[NCBI]
|
7.09823e-05
|
|
|
corneal dystrophy, epithelial basement membrane
|
[NCBI]
|
6.867e-05
|
|
|
ASMD
|
[NCBI]
|
6.48565e-05
|
|
|
RA
|
[NCBI]
|
6.31403e-05
|
|
|
wagr syndrome
|
[NCBI]
|
6.17799e-05
|
|
|
alport syndrome, autosomal recessive
|
[NCBI]
|
6.17799e-05
|
|
|
LADD
|
[NCBI]
|
6.0439e-05
|
|
|
CDL1
|
[NCBI]
|
6.0439e-05
|
|
|
morquio syndrome b
|
[NCBI]
|
5.92022e-05
|
|
|
plasminogen deficiency, type i
|
[NCBI]
|
5.92022e-05
|
|
|
KRT3
|
[NCBI]
|
5.78478e-05
|
|
|
OGN
|
[NCBI]
|
5.78478e-05
|
|
|
NCIE1
|
[NCBI]
|
5.69848e-05
|
|
|
KRT12
|
[NCBI]
|
5.33406e-05
|
|
|
MPV17
|
[NCBI]
|
5.33406e-05
|
|
|
CIPA
|
[NCBI]
|
5.33081e-05
|
|
|
NHS
|
[NCBI]
|
5.33081e-05
|
|
|
PALS
|
[NCBI]
|
5.25088e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
5.1748e-05
|
|
|
TKT
|
[NCBI]
|
5.16791e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
4.96647e-05
|
|
|
LCAT
|
[NCBI]
|
4.69253e-05
|
|
|
MCOPS7
|
[NCBI]
|
4.51755e-05
|
|
|
PFIC1
|
[NCBI]
|
4.42303e-05
|
|
|
MCOLN1
|
[NCBI]
|
4.372e-05
|
|
|
FOXC1
|
[NCBI]
|
4.18593e-05
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
4.18593e-05
|
|
|
DCN
|
[NCBI]
|
4.13098e-05
|
|
|
CMTC
|
[NCBI]
|
3.98701e-05
|
|
|
LI1
|
[NCBI]
|
3.82373e-05
|
|
|
PITX2
|
[NCBI]
|
3.81408e-05
|
|
|
CTNS
|
[NCBI]
|
3.73362e-05
|
|
|
RTS
|
[NCBI]
|
3.67642e-05
|
|
|
ZNF145
|
[NCBI]
|
3.63762e-05
|
|
|
ABCA1
|
[NCBI]
|
3.63762e-05
|
|
|
ALGS1
|
[NCBI]
|
3.32785e-05
|
|
|
SMS
|
[NCBI]
|
2.69261e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.65277e-05
|
|
|
GUSB
|
[NCBI]
|
2.56429e-05
|
|
|
fabry disease
|
[NCBI]
|
2.51918e-05
|
|
|
FBN1
|
[NCBI]
|
2.40013e-05
|
|
|
DRPLA
|
[NCBI]
|
2.1399e-05
|
|
|
PLG
|
[NCBI]
|
2.12641e-05
|
|
|
VIP
|
[NCBI]
|
2.1089e-05
|
|
|
NGFB
|
[NCBI]
|
2.0221e-05
|
|
|
MFS
|
[NCBI]
|
1.45227e-05
|
|
|
CTGF
|
[NCBI]
|
1.30165e-05
|
|
|
ADA
|
[NCBI]
|
6.17334e-06
|
|
|
PCNA
|
[NCBI]
|
5.92666e-06
|
|
|
TNF
|
[NCBI]
|
4.06932e-06
|
|
|
RP
|
[NCBI]
|
3.33752e-06
|
|
|
TH
|
[NCBI]
|
3.09548e-06
|
|
|
HGF
|
[NCBI]
|
2.1144e-06
|
|
|
VEGF
|
[NCBI]
|
4.27613e-07
|
|
|
CJD
|
[NCBI]
|
4.03014e-07
|
|
|
CEACAM5
|
[NCBI]
|
3.5225e-07
|
|