|
OMIM |
Link |
Information gain |
01 |
|
glaucoma-related pigment dispersion syndrome
|
[NCBI]
|
0.00303971
|
|
|
GLC3B
|
[NCBI]
|
0.00182137
|
|
|
GLC3A
|
[NCBI]
|
0.00170791
|
|
|
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss
|
[NCBI]
|
0.00152161
|
|
|
RIEG2
|
[NCBI]
|
0.00138638
|
|
|
microcoria, congenital
|
[NCBI]
|
0.000907885
|
|
|
armfield x-linked mental retardation syndrome
|
[NCBI]
|
0.000907885
|
|
|
CYP1B1
|
[NCBI]
|
0.000864181
|
|
|
GLC1A
|
[NCBI]
|
0.000788167
|
|
|
IRID2
|
[NCBI]
|
0.000717128
|
|
|
singleton-merten syndrome
|
[NCBI]
|
0.000690406
|
|
|
FOXC1
|
[NCBI]
|
0.000653512
|
|
|
XFS
|
[NCBI]
|
0.000650527
|
|
|
MYOC
|
[NCBI]
|
0.000643643
|
|
|
POAG
|
[NCBI]
|
0.000609984
|
|
|
RIEG1
|
[NCBI]
|
0.000569779
|
|
|
leri pleonosteosis
|
[NCBI]
|
0.000555675
|
|
|
MYP3
|
[NCBI]
|
0.000555675
|
|
|
GLC1C
|
[NCBI]
|
0.000516429
|
|
|
dyssegmental dysplasia, rolland-desbuquois type
|
[NCBI]
|
0.000437349
|
|
|
gapo syndrome
|
[NCBI]
|
0.000437349
|
|
|
OPTN
|
[NCBI]
|
0.000433626
|
|
|
IRID1
|
[NCBI]
|
0.000401923
|
|
|
basal ganglia calcification, idiopathic, childhood-onset
|
[NCBI]
|
0.000385833
|
|
|
VRNI
|
[NCBI]
|
0.000362511
|
|
|
glaucoma, normal tension, susceptibility to
|
[NCBI]
|
0.000342055
|
|
|
MYP2
|
[NCBI]
|
0.000336982
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000292795
|
|
|
peters anomaly
|
[NCBI]
|
0.000247085
|
|
|
frank-ter haar syndrome
|
[NCBI]
|
0.00022489
|
|
|
PITX2
|
[NCBI]
|
0.000223821
|
|
|
OCRL
|
[NCBI]
|
0.000220581
|
|
|
spastic paresis, glaucoma, and mental retardation
|
[NCBI]
|
0.000209502
|
|
|
SLE
|
[NCBI]
|
0.000185544
|
|
|
scheie syndrome
|
[NCBI]
|
0.000183333
|
|
|
PPCD1
|
[NCBI]
|
0.000183333
|
|
|
GEMSS
|
[NCBI]
|
0.000178572
|
|
|
lowry-maclean syndrome
|
[NCBI]
|
0.000178572
|
|
|
PPR
|
[NCBI]
|
0.000175114
|
|
|
behcet syndrome
|
[NCBI]
|
0.000160786
|
|
|
STL1
|
[NCBI]
|
0.000143878
|
|
|
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
|
[NCBI]
|
0.00014174
|
|
|
OPTC
|
[NCBI]
|
0.000139833
|
|
|
OLFM3
|
[NCBI]
|
0.000139833
|
|
|
short syndrome
|
[NCBI]
|
0.000136727
|
|
|
sturge-weber syndrome
|
[NCBI]
|
0.000125181
|
|
|
SLC4A4
|
[NCBI]
|
0.000112289
|
|
|
OCP
|
[NCBI]
|
0.000112042
|
|
|
bowen syndrome of multiple malformations
|
[NCBI]
|
0.000104693
|
|
|
friedreich ataxia and congenital glaucoma
|
[NCBI]
|
0.000104693
|
|
|
tetralogy of fallot and glaucoma
|
[NCBI]
|
0.000104693
|
|
|
glaucoma and sleep apnea
|
[NCBI]
|
0.000104693
|
|
|
microcornea, glaucoma, and absent frontal sinuses
|
[NCBI]
|
0.000104693
|
|
|
microspherophakia with hernia
|
[NCBI]
|
0.000104693
|
|
|
retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma
|
[NCBI]
|
0.000104693
|
|
|
ackerman syndrome
|
[NCBI]
|
0.000104693
|
|
|
glaucoma with elevated episcleral venous pressure
|
[NCBI]
|
0.000104693
|
|
|
iridogoniodysgenesis and skeletal anomalies
|
[NCBI]
|
0.000104693
|
|
|
dyssegmental dysplasia with glaucoma
|
[NCBI]
|
0.000104693
|
|
|
GFAP
|
[NCBI]
|
0.000103604
|
|
|
EVR1
|
[NCBI]
|
9.58061e-05
|
|
|
dwarfism with stiff joints and ocular abnormalities
|
[NCBI]
|
8.22454e-05
|
|
|
aniridia, partial, with unilateral renal agenesis and psychomotor retardation
|
[NCBI]
|
8.22454e-05
|
|
|
PPAB
|
[NCBI]
|
8.22454e-05
|
|
|
histiocytic dermatoarthritis
|
[NCBI]
|
8.22454e-05
|
|
|
FOXC2
|
[NCBI]
|
7.6426e-05
|
|
|
AN2
|
[NCBI]
|
7.39561e-05
|
|
|
OPA1
|
[NCBI]
|
7.33846e-05
|
|
|
GMDS
|
[NCBI]
|
6.98778e-05
|
|
|
NPS
|
[NCBI]
|
6.44392e-05
|
|
|
FOXF1
|
[NCBI]
|
5.61058e-05
|
|
|
OCLM
|
[NCBI]
|
5.61058e-05
|
|
|
FOXL1
|
[NCBI]
|
5.61058e-05
|
|
|
FOXF2
|
[NCBI]
|
5.61058e-05
|
|
|
phace association
|
[NCBI]
|
5.60088e-05
|
|
|
ectopia lentis, isolated
|
[NCBI]
|
5.60088e-05
|
|
|
AN1
|
[NCBI]
|
5.60088e-05
|
|
|
amyloidosis, familial visceral
|
[NCBI]
|
5.40025e-05
|
|
|
CMT4B2
|
[NCBI]
|
5.40025e-05
|
|
|
WT1
|
[NCBI]
|
5.36527e-05
|
|
|
ASMD
|
[NCBI]
|
5.22229e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
5.22229e-05
|
|
|
growth-mental deficiency syndrome of myhre
|
[NCBI]
|
5.22229e-05
|
|
|
DYNLL1
|
[NCBI]
|
5.09131e-05
|
|
|
LOXL1
|
[NCBI]
|
5.09131e-05
|
|
|
WZS
|
[NCBI]
|
4.7847e-05
|
|
|
CDL1
|
[NCBI]
|
4.7847e-05
|
|
|
CA12
|
[NCBI]
|
4.7544e-05
|
|
|
MCOPS2
|
[NCBI]
|
4.66241e-05
|
|
|
WGN1
|
[NCBI]
|
4.54906e-05
|
|
|
FGF19
|
[NCBI]
|
4.50411e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
4.34459e-05
|
|
|
NF1
|
[NCBI]
|
4.31596e-05
|
|
|
SBF2
|
[NCBI]
|
4.30482e-05
|
|
|
FBN1
|
[NCBI]
|
4.15769e-05
|
|
|
TFAP2A
|
[NCBI]
|
4.13925e-05
|
|
|
CTGF
|
[NCBI]
|
4.09337e-05
|
|
|
ESCS
|
[NCBI]
|
4.08132e-05
|
|
|
BDNF
|
[NCBI]
|
4.03661e-05
|
|
|
SELE
|
[NCBI]
|
3.99763e-05
|
|
|
HSS
|
[NCBI]
|
3.78894e-05
|
|
|
STGD1
|
[NCBI]
|
3.48886e-05
|
|
|
COL11A1
|
[NCBI]
|
3.41808e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
3.23948e-05
|
|
|
ODDD
|
[NCBI]
|
3.15055e-05
|
|
|
MEB
|
[NCBI]
|
3.06676e-05
|
|
|
CMTC
|
[NCBI]
|
2.77356e-05
|
|
|
pta deficiency
|
[NCBI]
|
2.56122e-05
|
|
|
DM2
|
[NCBI]
|
2.55932e-05
|
|
|
SLC18A3
|
[NCBI]
|
2.5036e-05
|
|
|
RSTS
|
[NCBI]
|
2.32565e-05
|
|
|
hurler syndrome
|
[NCBI]
|
2.23364e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
2.10201e-05
|
|
|
PAX6
|
[NCBI]
|
1.9997e-05
|
|
|
TNF
|
[NCBI]
|
1.91174e-05
|
|
|
PTGS2
|
[NCBI]
|
1.9079e-05
|
|
|
RP
|
[NCBI]
|
1.90763e-05
|
|
|
TYR
|
[NCBI]
|
1.86534e-05
|
|
|
COL2A1
|
[NCBI]
|
1.74882e-05
|
|
|
SLPI
|
[NCBI]
|
1.63547e-05
|
|
|
homocystinuria
|
[NCBI]
|
1.43784e-05
|
|
|
ZS
|
[NCBI]
|
1.39591e-05
|
|
|
TTR
|
[NCBI]
|
1.22755e-05
|
|
|
PEDF
|
[NCBI]
|
1.11855e-05
|
|
|
GJA1
|
[NCBI]
|
1.04965e-05
|
|
|
FGF7
|
[NCBI]
|
8.12119e-06
|
|
|
CP
|
[NCBI]
|
8.0856e-06
|
|
|
NGFB
|
[NCBI]
|
7.42474e-06
|
|
|
NPPA
|
[NCBI]
|
6.70855e-06
|
|
|
COMT
|
[NCBI]
|
4.37076e-06
|
|
|
TF
|
[NCBI]
|
4.26426e-06
|
|
|
TH
|
[NCBI]
|
2.66883e-06
|
|
|
ACHE
|
[NCBI]
|
2.62854e-06
|
|
|
EGFR
|
[NCBI]
|
1.57318e-06
|
|
|
CHAT
|
[NCBI]
|
1.38517e-06
|
|
|
NPY
|
[NCBI]
|
1.20059e-06
|
|
|
MBP
|
[NCBI]
|
6.53506e-07
|
|
|
HGF
|
[NCBI]
|
5.20306e-07
|
|
|
AR
|
[NCBI]
|
4.78236e-07
|
|
|
TNFSF6
|
[NCBI]
|
2.10266e-07
|
|
|
APOE
|
[NCBI]
|
1.94499e-07
|
|
|
VIP
|
[NCBI]
|
1.35526e-07
|
|
|
FA
|
[NCBI]
|
7.42834e-08
|
|
|
EGF
|
[NCBI]
|
5.45824e-08
|
|
|
PWS
|
[NCBI]
|
4.14024e-08
|
|
|
CAT
|
[NCBI]
|
2.24269e-09
|
|
|
EPO
|
[NCBI]
|
1.95966e-10
|
|