|
OMIM |
Link |
Information gain |
01 |
|
megalocornea-mental retardation syndrome
|
[NCBI]
|
0.0113447
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.00422296
|
|
|
CNA1
|
[NCBI]
|
0.00391317
|
|
|
CHED1
|
[NCBI]
|
0.00241862
|
|
|
NNO1
|
[NCBI]
|
0.00241862
|
|
|
CND
|
[NCBI]
|
0.00222636
|
|
|
CDB2
|
[NCBI]
|
0.00216732
|
|
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.00207099
|
|
|
MACOM
|
[NCBI]
|
0.00179953
|
|
|
cataract-microcornea syndrome
|
[NCBI]
|
0.00129247
|
|
|
MCOPS1
|
[NCBI]
|
0.00116767
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.00111071
|
|
|
astigmatism
|
[NCBI]
|
0.00111071
|
|
|
cornea guttata with anterior polar cataracts
|
[NCBI]
|
0.00111071
|
|
|
MCDC1
|
[NCBI]
|
0.000876674
|
|
|
MGC1
|
[NCBI]
|
0.000801288
|
|
|
CDGG1
|
[NCBI]
|
0.000754085
|
|
|
MCOPS4
|
[NCBI]
|
0.000685481
|
|
|
KTCN1
|
[NCBI]
|
0.000683173
|
|
|
corneal dystrophy, epithelial basement membrane
|
[NCBI]
|
0.000656878
|
|
|
CDL1
|
[NCBI]
|
0.000631752
|
|
|
FECD2
|
[NCBI]
|
0.000610829
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.000610829
|
|
|
cutis laxa, corneal clouding, and mental retardation
|
[NCBI]
|
0.000555722
|
|
|
MCOPS6
|
[NCBI]
|
0.000512128
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
0.000509751
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
0.000497613
|
|
|
CDA
|
[NCBI]
|
0.000488176
|
|
|
peters-plus syndrome
|
[NCBI]
|
0.000488176
|
|
|
VEGF
|
[NCBI]
|
0.000483271
|
|
|
MCOP1
|
[NCBI]
|
0.000476141
|
|
|
OCP
|
[NCBI]
|
0.000471359
|
|
|
CDB1
|
[NCBI]
|
0.000470209
|
|
|
CFEOM3
|
[NCBI]
|
0.00044556
|
|
|
CNA2
|
[NCBI]
|
0.000419799
|
|
|
EGF
|
[NCBI]
|
0.000412357
|
|
|
RA
|
[NCBI]
|
0.000407172
|
|
|
PPCD1
|
[NCBI]
|
0.000399491
|
|
|
corneal dystrophy, juvenile epithelial, of meesmann
|
[NCBI]
|
0.000388283
|
|
|
CHED2
|
[NCBI]
|
0.000365887
|
|
|
sjogren syndrome
|
[NCBI]
|
0.000355885
|
|
|
cystinosis, adult nonnephropathic
|
[NCBI]
|
0.000348374
|
|
|
SLE
|
[NCBI]
|
0.000343383
|
|
|
arcus corneae
|
[NCBI]
|
0.000322125
|
|
|
MCOP3
|
[NCBI]
|
0.000322125
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000308593
|
|
|
amyloidosis v
|
[NCBI]
|
0.000301578
|
|
|
MEN2B
|
[NCBI]
|
0.000245525
|
|
|
CSCD
|
[NCBI]
|
0.000243762
|
|
|
corneal fleck dystrophy
|
[NCBI]
|
0.000243762
|
|
|
mucolipidosis iv
|
[NCBI]
|
0.000225632
|
|
|
MCOPS7
|
[NCBI]
|
0.000212637
|
|
|
WARBM
|
[NCBI]
|
0.00020395
|
|
|
bietti crystalline corneoretinal dystrophy
|
[NCBI]
|
0.000195241
|
|
|
CF
|
[NCBI]
|
0.00019178
|
|
|
TKT
|
[NCBI]
|
0.00019173
|
|
|
KERA
|
[NCBI]
|
0.000190073
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
0.000187724
|
|
|
TGFBI
|
[NCBI]
|
0.000184977
|
|
|
ASMD
|
[NCBI]
|
0.000175218
|
|
|
FED
|
[NCBI]
|
0.000169897
|
|
|
ALGS1
|
[NCBI]
|
0.000169776
|
|
|
spinocerebellar degeneration and corneal dystrophy
|
[NCBI]
|
0.000160981
|
|
|
MCOP2
|
[NCBI]
|
0.000160981
|
|
|
dysgenesis mesodermalis corneae et sclerae
|
[NCBI]
|
0.000160981
|
|
|
corneal degeneration, band-shaped spheroid
|
[NCBI]
|
0.000160981
|
|
|
aniridia, microcornea, and spontaneously reabsorbed cataract
|
[NCBI]
|
0.000160981
|
|
|
microcornea, glaucoma, and absent frontal sinuses
|
[NCBI]
|
0.000160981
|
|
|
CDL3A
|
[NCBI]
|
0.000160981
|
|
|
wilson disease
|
[NCBI]
|
0.000155591
|
|
|
NHS
|
[NCBI]
|
0.000149103
|
|
|
KFSD
|
[NCBI]
|
0.000149103
|
|
|
KRT3
|
[NCBI]
|
0.000148656
|
|
|
KRT12
|
[NCBI]
|
0.000136257
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
0.000134158
|
|
|
FGF7
|
[NCBI]
|
0.000130861
|
|
|
ODDD
|
[NCBI]
|
0.000129191
|
|
|
corneal dystrophy and perceptive deafness
|
[NCBI]
|
0.0001218
|
|
|
PPCD3
|
[NCBI]
|
0.0001218
|
|
|
spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia
|
[NCBI]
|
0.0001218
|
|
|
MCOPS5
|
[NCBI]
|
0.0001218
|
|
|
MCOPCB4
|
[NCBI]
|
0.0001218
|
|
|
FDH
|
[NCBI]
|
0.000118518
|
|
|
CHST6
|
[NCBI]
|
0.000115889
|
|
|
mucopolysaccharidoses, unclassified types
|
[NCBI]
|
0.000107071
|
|
|
FECD1
|
[NCBI]
|
0.000107071
|
|
|
HSAN5
|
[NCBI]
|
0.000107071
|
|
|
LORD
|
[NCBI]
|
0.000107071
|
|
|
keratoderma, palmoplantar, with deafness
|
[NCBI]
|
0.000107071
|
|
|
keratitis, hereditary
|
[NCBI]
|
0.000107071
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000104479
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
9.75404e-05
|
|
|
coloboma of optic nerve
|
[NCBI]
|
9.75404e-05
|
|
|
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
|
[NCBI]
|
9.75404e-05
|
|
|
AN2
|
[NCBI]
|
9.44342e-05
|
|
|
APS1
|
[NCBI]
|
9.32565e-05
|
|
|
TNC
|
[NCBI]
|
9.18024e-05
|
|
|
peters anomaly
|
[NCBI]
|
9.0478e-05
|
|
|
winchester syndrome
|
[NCBI]
|
9.0478e-05
|
|
|
short syndrome
|
[NCBI]
|
8.02218e-05
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
8.02218e-05
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
7.62568e-05
|
|
|
AN1
|
[NCBI]
|
7.28024e-05
|
|
|
MCOPS9
|
[NCBI]
|
7.28024e-05
|
|
|
epidermolysis bullosa simplex and limb-girdle muscular dystrophy
|
[NCBI]
|
7.28024e-05
|
|
|
FOXC1
|
[NCBI]
|
7.26455e-05
|
|
|
coloboma, ocular
|
[NCBI]
|
6.97443e-05
|
|
|
COL8A2
|
[NCBI]
|
6.80964e-05
|
|
|
IRID1
|
[NCBI]
|
6.70027e-05
|
|
|
XFS
|
[NCBI]
|
6.70027e-05
|
|
|
scheie syndrome
|
[NCBI]
|
6.70027e-05
|
|
|
IRID2
|
[NCBI]
|
6.70027e-05
|
|
|
HSS
|
[NCBI]
|
6.70027e-05
|
|
|
WGN1
|
[NCBI]
|
6.45199e-05
|
|
|
MCOPS3
|
[NCBI]
|
6.45199e-05
|
|
|
ED2
|
[NCBI]
|
6.22526e-05
|
|
|
MCOPS2
|
[NCBI]
|
6.22526e-05
|
|
|
DCN
|
[NCBI]
|
6.08323e-05
|
|
|
OGFR
|
[NCBI]
|
6.05917e-05
|
|
|
NBIA1
|
[NCBI]
|
5.64446e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
5.3198e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
5.3198e-05
|
|
|
CYP1B1
|
[NCBI]
|
5.21219e-05
|
|
|
EKV
|
[NCBI]
|
5.17196e-05
|
|
|
ALDH3A1
|
[NCBI]
|
4.92536e-05
|
|
|
ENPEP
|
[NCBI]
|
4.829e-05
|
|
|
IGER
|
[NCBI]
|
4.77502e-05
|
|
|
POF1
|
[NCBI]
|
4.77502e-05
|
|
|
EBR1
|
[NCBI]
|
4.65584e-05
|
|
|
PAX6
|
[NCBI]
|
4.45576e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
4.43382e-05
|
|
|
LACRT
|
[NCBI]
|
4.40078e-05
|
|
|
COL24A1
|
[NCBI]
|
4.40078e-05
|
|
|
GLC1A
|
[NCBI]
|
4.23076e-05
|
|
|
NGFB
|
[NCBI]
|
4.17903e-05
|
|
|
RIEG1
|
[NCBI]
|
4.13545e-05
|
|
|
HGF
|
[NCBI]
|
3.99951e-05
|
|
|
LCAT
|
[NCBI]
|
3.97811e-05
|
|
|
PEDF
|
[NCBI]
|
3.81612e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
3.71034e-05
|
|
|
AQP5
|
[NCBI]
|
3.60506e-05
|
|
|
PITX2
|
[NCBI]
|
3.50884e-05
|
|
|
SCS
|
[NCBI]
|
3.48911e-05
|
|
|
MUC16
|
[NCBI]
|
3.40401e-05
|
|
|
RAX
|
[NCBI]
|
3.40401e-05
|
|
|
SH3BP4
|
[NCBI]
|
3.40401e-05
|
|
|
COL16A1
|
[NCBI]
|
3.40401e-05
|
|
|
GMDS
|
[NCBI]
|
3.40401e-05
|
|
|
ALOX15B
|
[NCBI]
|
3.40401e-05
|
|
|
FOXL1
|
[NCBI]
|
3.40401e-05
|
|
|
AKR1B1
|
[NCBI]
|
3.31568e-05
|
|
|
PRL
|
[NCBI]
|
3.15308e-05
|
|
|
EGR4
|
[NCBI]
|
3.02878e-05
|
|
|
PGLYRP2
|
[NCBI]
|
3.02878e-05
|
|
|
LGALS7
|
[NCBI]
|
3.02878e-05
|
|
|
UBC
|
[NCBI]
|
3.02878e-05
|
|
|
DSPG3
|
[NCBI]
|
3.02878e-05
|
|
|
CHST5
|
[NCBI]
|
3.02878e-05
|
|
|
NTRK1
|
[NCBI]
|
2.97938e-05
|
|
|
VIP
|
[NCBI]
|
2.8903e-05
|
|
|
NS1
|
[NCBI]
|
2.83047e-05
|
|
|
ROCK2
|
[NCBI]
|
2.78567e-05
|
|
|
HIF3A
|
[NCBI]
|
2.78567e-05
|
|
|
DNAH5
|
[NCBI]
|
2.78567e-05
|
|
|
FOXF2
|
[NCBI]
|
2.78567e-05
|
|
|
CCK
|
[NCBI]
|
2.71844e-05
|
|
|
SP3
|
[NCBI]
|
2.6053e-05
|
|
|
CASP7
|
[NCBI]
|
2.6053e-05
|
|
|
PIP5K3
|
[NCBI]
|
2.6053e-05
|
|
|
LAMA4
|
[NCBI]
|
2.6053e-05
|
|
|
CCT
|
[NCBI]
|
2.6053e-05
|
|
|
F7R
|
[NCBI]
|
2.6053e-05
|
|
|
CTGF
|
[NCBI]
|
2.55107e-05
|
|
|
BDNF
|
[NCBI]
|
2.48644e-05
|
|
|
TP53BP2
|
[NCBI]
|
2.46189e-05
|
|
|
ANGPTL3
|
[NCBI]
|
2.46189e-05
|
|
|
RAB3GAP1
|
[NCBI]
|
2.46189e-05
|
|
|
MG
|
[NCBI]
|
2.36594e-05
|
|
|
SCG2
|
[NCBI]
|
2.3429e-05
|
|
|
frank-ter haar syndrome
|
[NCBI]
|
2.3429e-05
|
|
|
LUM
|
[NCBI]
|
2.3429e-05
|
|
|
ROCK1
|
[NCBI]
|
2.3429e-05
|
|
|
MAF
|
[NCBI]
|
2.3429e-05
|
|
|
CTSL2
|
[NCBI]
|
2.3429e-05
|
|
|
TCF8
|
[NCBI]
|
2.3429e-05
|
|
|
NPY
|
[NCBI]
|
2.26319e-05
|
|
|
PI5
|
[NCBI]
|
2.24126e-05
|
|
|
NPC1
|
[NCBI]
|
2.1831e-05
|
|
|
AQP1
|
[NCBI]
|
2.15932e-05
|
|
|
FOXF1
|
[NCBI]
|
2.1526e-05
|
|
|
BCL2L1
|
[NCBI]
|
2.1526e-05
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
2.1526e-05
|
|
|
TNNI2
|
[NCBI]
|
2.1526e-05
|
|
|
COL5A2
|
[NCBI]
|
2.1526e-05
|
|
|
GFAP
|
[NCBI]
|
2.10043e-05
|
|
|
SLC4A4
|
[NCBI]
|
2.07401e-05
|
|
|
COL4A4
|
[NCBI]
|
2.07401e-05
|
|
|
PITX3
|
[NCBI]
|
2.07401e-05
|
|
|
OGN
|
[NCBI]
|
2.07401e-05
|
|
|
COL6A3
|
[NCBI]
|
2.00347e-05
|
|
|
FMOD
|
[NCBI]
|
2.00347e-05
|
|
|
farber lipogranulomatosis
|
[NCBI]
|
2.00347e-05
|
|
|
COL11A1
|
[NCBI]
|
2.00347e-05
|
|
|
TFAP2A
|
[NCBI]
|
1.93951e-05
|
|
|
DNAH11
|
[NCBI]
|
1.88103e-05
|
|
|
BAI1
|
[NCBI]
|
1.88103e-05
|
|
|
MMP7
|
[NCBI]
|
1.88103e-05
|
|
|
RHOA
|
[NCBI]
|
1.82717e-05
|
|
|
ANGPT2
|
[NCBI]
|
1.82717e-05
|
|
|
AVP
|
[NCBI]
|
1.79752e-05
|
|
|
SMAD3
|
[NCBI]
|
1.77728e-05
|
|
|
DDR1
|
[NCBI]
|
1.73084e-05
|
|
|
SMAD2
|
[NCBI]
|
1.68739e-05
|
|
|
FOXC2
|
[NCBI]
|
1.68739e-05
|
|
|
BMP7
|
[NCBI]
|
1.68739e-05
|
|
|
MIF
|
[NCBI]
|
1.6466e-05
|
|
|
fabry disease
|
[NCBI]
|
1.62954e-05
|
|
|
MBP
|
[NCBI]
|
1.57664e-05
|
|
|
TP73L
|
[NCBI]
|
1.57185e-05
|
|
|
COL4A1
|
[NCBI]
|
1.53742e-05
|
|
|
KLF6
|
[NCBI]
|
1.53742e-05
|
|
|
COL17A1
|
[NCBI]
|
1.44384e-05
|
|
|
FLT1
|
[NCBI]
|
1.44384e-05
|
|
|
GSN
|
[NCBI]
|
1.44384e-05
|
|
|
GJA8
|
[NCBI]
|
1.44384e-05
|
|
|
FGF2
|
[NCBI]
|
1.40616e-05
|
|
|
COL4A3
|
[NCBI]
|
1.38821e-05
|
|
|
IPF1
|
[NCBI]
|
1.38821e-05
|
|
|
GJA1
|
[NCBI]
|
1.33051e-05
|
|
|
CFLAR
|
[NCBI]
|
1.28965e-05
|
|
|
CHUK
|
[NCBI]
|
1.26724e-05
|
|
|
MMP3
|
[NCBI]
|
1.26724e-05
|
|
|
TNFRSF14
|
[NCBI]
|
1.26724e-05
|
|
|
PSIP1
|
[NCBI]
|
1.2456e-05
|
|
|
CCR5
|
[NCBI]
|
1.22469e-05
|
|
|
TIMP1
|
[NCBI]
|
1.18488e-05
|
|
|
MPO
|
[NCBI]
|
1.16059e-05
|
|
|
INHBA
|
[NCBI]
|
1.14749e-05
|
|
|
IP
|
[NCBI]
|
1.13176e-05
|
|
|
CPB2
|
[NCBI]
|
1.12962e-05
|
|
|
SST
|
[NCBI]
|
1.11724e-05
|
|
|
DSTN
|
[NCBI]
|
1.0954e-05
|
|
|
EGR1
|
[NCBI]
|
1.0954e-05
|
|
|
BGN
|
[NCBI]
|
1.0954e-05
|
|
|
ASL
|
[NCBI]
|
1.0954e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
1.04747e-05
|
|
|
COMP
|
[NCBI]
|
1.01968e-05
|
|
|
DCT
|
[NCBI]
|
9.48849e-06
|
|
|
MMP2
|
[NCBI]
|
9.11268e-06
|
|
|
LPL
|
[NCBI]
|
9.09824e-06
|
|
|
NPPA
|
[NCBI]
|
8.16171e-06
|
|
|
MYOC
|
[NCBI]
|
8.11702e-06
|
|
|
GPT
|
[NCBI]
|
7.63401e-06
|
|
|
AR
|
[NCBI]
|
7.02649e-06
|
|
|
CLU
|
[NCBI]
|
7.02513e-06
|
|
|
STAT6
|
[NCBI]
|
7.02513e-06
|
|
|
MVP
|
[NCBI]
|
6.94379e-06
|
|
|
MFS
|
[NCBI]
|
6.94346e-06
|
|
|
TNFRSF1A
|
[NCBI]
|
6.86375e-06
|
|
|
BSG
|
[NCBI]
|
6.78497e-06
|
|
|
CJD
|
[NCBI]
|
6.60327e-06
|
|
|
TH
|
[NCBI]
|
6.45882e-06
|
|
|
PTGS2
|
[NCBI]
|
6.12782e-06
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
6.06007e-06
|
|
|
TNF
|
[NCBI]
|
5.99163e-06
|
|
|
CCL22
|
[NCBI]
|
5.92742e-06
|
|
|
ABCC2
|
[NCBI]
|
5.55092e-06
|
|
|
GUSB
|
[NCBI]
|
5.4911e-06
|
|
|
GJB2
|
[NCBI]
|
5.1482e-06
|
|
|
RNASE2
|
[NCBI]
|
4.98639e-06
|
|
|
PLG
|
[NCBI]
|
4.88184e-06
|
|
|
LEP
|
[NCBI]
|
4.77982e-06
|
|
|
MBL2
|
[NCBI]
|
4.63136e-06
|
|
|
TNFSF6
|
[NCBI]
|
4.42936e-06
|
|
|
ACHE
|
[NCBI]
|
4.22873e-06
|
|
|
KDR
|
[NCBI]
|
4.1727e-06
|
|
|
RBP1
|
[NCBI]
|
4.12965e-06
|
|
|
CAT
|
[NCBI]
|
3.35542e-06
|
|
|
ADA
|
[NCBI]
|
2.92488e-06
|
|
|
RP
|
[NCBI]
|
2.64322e-06
|
|
|
GNRH1
|
[NCBI]
|
2.55848e-06
|
|
|
RNASE3
|
[NCBI]
|
2.37316e-06
|
|
|
G6PD
|
[NCBI]
|
2.25148e-06
|
|
|
TLR4
|
[NCBI]
|
2.23804e-06
|
|
|
FMF
|
[NCBI]
|
2.11483e-06
|
|
|
EGFR
|
[NCBI]
|
1.12741e-06
|
|
|
TNFSF10
|
[NCBI]
|
7.50302e-07
|
|
|
ADCYAP1
|
[NCBI]
|
7.37142e-07
|
|
|
GAPDH
|
[NCBI]
|
5.99158e-07
|
|
|
SDC2
|
[NCBI]
|
5.89595e-07
|
|
|
XDH
|
[NCBI]
|
4.54032e-07
|
|
|
CFTR
|
[NCBI]
|
1.94517e-07
|
|
|
PTK2
|
[NCBI]
|
1.73913e-07
|
|
|
OSM
|
[NCBI]
|
1.41135e-07
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
1.06764e-07
|
|
|
ABCC1
|
[NCBI]
|
7.35257e-08
|
|
|
PCNA
|
[NCBI]
|
1.63409e-08
|
|
|
GAL
|
[NCBI]
|
4.81303e-10
|
|