|
OMIM |
Link |
Information gain |
01 |
|
cataract and cardiomyopathy
|
[NCBI]
|
0.00473977
|
|
|
CCA1
|
[NCBI]
|
0.00446185
|
|
|
CTPP1
|
[NCBI]
|
0.00446185
|
|
|
CTAA1
|
[NCBI]
|
0.00371336
|
|
|
cataract, congenital or juvenile
|
[NCBI]
|
0.00328968
|
|
|
CCV
|
[NCBI]
|
0.00296684
|
|
|
CTAA2
|
[NCBI]
|
0.00296684
|
|
|
cataract, central saccular, with sutural opacities
|
[NCBI]
|
0.00222227
|
|
|
cataract, age-related cortical
|
[NCBI]
|
0.00222227
|
|
|
cataract, autosomal recessive, early-onset, pulverulent
|
[NCBI]
|
0.00222227
|
|
|
NHS
|
[NCBI]
|
0.0017838
|
|
|
AKR1B1
|
[NCBI]
|
0.00157162
|
|
|
cataract, autosomal recessive congenital 2
|
[NCBI]
|
0.00147962
|
|
|
MCOPCT1
|
[NCBI]
|
0.00147962
|
|
|
mucoepithelial dysplasia, hereditary
|
[NCBI]
|
0.0011808
|
|
|
vitreoretinal degeneration, snowflake type
|
[NCBI]
|
0.0011808
|
|
|
SPG9
|
[NCBI]
|
0.0011808
|
|
|
GJA8
|
[NCBI]
|
0.00116228
|
|
|
MSS
|
[NCBI]
|
0.00106709
|
|
|
VRCP
|
[NCBI]
|
0.00104652
|
|
|
CRYGD
|
[NCBI]
|
0.00091662
|
|
|
FTL
|
[NCBI]
|
0.000908279
|
|
|
CZP1
|
[NCBI]
|
0.000800512
|
|
|
RA
|
[NCBI]
|
0.000788872
|
|
|
congenital cataracts, facial dysmorphism, and neuropathy
|
[NCBI]
|
0.000776036
|
|
|
hyperferritinemia-cataract syndrome
|
[NCBI]
|
0.000747881
|
|
|
olivopontocerebellar atrophy ii, autosomal recessive
|
[NCBI]
|
0.00073887
|
|
|
cataract, crystalline coralliform
|
[NCBI]
|
0.00073887
|
|
|
crome syndrome
|
[NCBI]
|
0.00073887
|
|
|
CATCN1
|
[NCBI]
|
0.00073887
|
|
|
CTPP5
|
[NCBI]
|
0.00073887
|
|
|
cataract, nuclear progressive
|
[NCBI]
|
0.00073887
|
|
|
cornea guttata with anterior polar cataracts
|
[NCBI]
|
0.00073887
|
|
|
cataract, ataxia, short stature, and mental retardation
|
[NCBI]
|
0.00073887
|
|
|
leg, absence deformity of, with congenital cataract
|
[NCBI]
|
0.00073887
|
|
|
CRYAA
|
[NCBI]
|
0.000732718
|
|
|
GJA3
|
[NCBI]
|
0.000732718
|
|
|
cataract-microcornea syndrome
|
[NCBI]
|
0.000711391
|
|
|
galactokinase deficiency
|
[NCBI]
|
0.000703438
|
|
|
CRYGC
|
[NCBI]
|
0.000671482
|
|
|
CCA2
|
[NCBI]
|
0.000622313
|
|
|
CZP3
|
[NCBI]
|
0.000622313
|
|
|
cataract, lamellar
|
[NCBI]
|
0.000622313
|
|
|
CRYBB2
|
[NCBI]
|
0.000556574
|
|
|
BFSP2
|
[NCBI]
|
0.000549108
|
|
|
SLE
|
[NCBI]
|
0.000546587
|
|
|
DM2
|
[NCBI]
|
0.000542901
|
|
|
cataract, congenital, with mental impairment and dentate gyrus atrophy
|
[NCBI]
|
0.000522339
|
|
|
MIP
|
[NCBI]
|
0.000487969
|
|
|
CRYBA1
|
[NCBI]
|
0.000487969
|
|
|
HSS
|
[NCBI]
|
0.000464818
|
|
|
Ii
|
[NCBI]
|
0.000460488
|
|
|
CTPP3
|
[NCBI]
|
0.000444291
|
|
|
CCZS
|
[NCBI]
|
0.000444291
|
|
|
immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum
|
[NCBI]
|
0.000441501
|
|
|
martsolf syndrome
|
[NCBI]
|
0.000440617
|
|
|
NHS
|
[NCBI]
|
0.000426862
|
|
|
OCRL
|
[NCBI]
|
0.000412413
|
|
|
MCOPS4
|
[NCBI]
|
0.000389505
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.000389505
|
|
|
ectopia lentis with ectopia of pupil
|
[NCBI]
|
0.000389505
|
|
|
woolly hair, autosomal dominant
|
[NCBI]
|
0.000389505
|
|
|
koilonychia, hereditary
|
[NCBI]
|
0.000389505
|
|
|
nievergelt syndrome
|
[NCBI]
|
0.000389505
|
|
|
NF2
|
[NCBI]
|
0.000382852
|
|
|
MCOPS2
|
[NCBI]
|
0.000378831
|
|
|
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
|
[NCBI]
|
0.000376537
|
|
|
GCNT2
|
[NCBI]
|
0.000365787
|
|
|
HSF4
|
[NCBI]
|
0.000365787
|
|
|
cataract, autosomal dominant, multiple types 1
|
[NCBI]
|
0.000355345
|
|
|
CCL
|
[NCBI]
|
0.000355345
|
|
|
PITX3
|
[NCBI]
|
0.000355272
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.000351208
|
|
|
hydroxykynureninuria
|
[NCBI]
|
0.000351208
|
|
|
CRYAB
|
[NCBI]
|
0.000349522
|
|
|
CF
|
[NCBI]
|
0.000330455
|
|
|
NNO1
|
[NCBI]
|
0.00032098
|
|
|
acanthosis nigricans
|
[NCBI]
|
0.00032098
|
|
|
LIM2
|
[NCBI]
|
0.000304743
|
|
|
CCT
|
[NCBI]
|
0.000304743
|
|
|
MCOPS6
|
[NCBI]
|
0.000296083
|
|
|
CRYGA
|
[NCBI]
|
0.000277891
|
|
|
CRYBA4
|
[NCBI]
|
0.000277891
|
|
|
oculocerebral syndrome with hypopigmentation
|
[NCBI]
|
0.000274975
|
|
|
cataract, age-related nuclear
|
[NCBI]
|
0.000266444
|
|
|
optic atrophy 3, autosomal dominant
|
[NCBI]
|
0.000266444
|
|
|
WARBM
|
[NCBI]
|
0.000265724
|
|
|
ASMD
|
[NCBI]
|
0.00024665
|
|
|
MCOP1
|
[NCBI]
|
0.000240625
|
|
|
VRNI
|
[NCBI]
|
0.000230552
|
|
|
MCOPS1
|
[NCBI]
|
0.000226306
|
|
|
renal failure, progressive, with hypertension
|
[NCBI]
|
0.000213424
|
|
|
RCDP1
|
[NCBI]
|
0.000208903
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
0.000196519
|
|
|
CHMP4B
|
[NCBI]
|
0.000182752
|
|
|
SORD
|
[NCBI]
|
0.000182752
|
|
|
hypomyelination and congenital cataract
|
[NCBI]
|
0.000177586
|
|
|
cataract, crystalline aculeiform
|
[NCBI]
|
0.000177586
|
|
|
ataxia-microcephaly-cataract syndrome
|
[NCBI]
|
0.000177586
|
|
|
cataract, nonnuclear polymorphic congenital, autosomal dominant
|
[NCBI]
|
0.000177586
|
|
|
CCA3
|
[NCBI]
|
0.000177586
|
|
|
CLSD
|
[NCBI]
|
0.000177586
|
|
|
cataract-ataxia-deafness-retardation syndrome
|
[NCBI]
|
0.000177586
|
|
|
microcephalic primordial dwarfism, toriello type
|
[NCBI]
|
0.000177586
|
|
|
spondyloocular syndrome, autosomal recessive
|
[NCBI]
|
0.000177586
|
|
|
microphthalmia, isolated, with cataract 4
|
[NCBI]
|
0.000177586
|
|
|
cataract, autosomal dominant
|
[NCBI]
|
0.000177586
|
|
|
uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly
|
[NCBI]
|
0.000177586
|
|
|
cataract, lamellar 2
|
[NCBI]
|
0.000177586
|
|
|
GALK1
|
[NCBI]
|
0.000176959
|
|
|
glaucoma-related pigment dispersion syndrome
|
[NCBI]
|
0.000172194
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.000172194
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
0.00016392
|
|
|
CRYBB3
|
[NCBI]
|
0.000160413
|
|
|
CRYBB1
|
[NCBI]
|
0.000149344
|
|
|
STL1
|
[NCBI]
|
0.000148643
|
|
|
cochleosaccular degeneration of the inner ear with progressive cataracts
|
[NCBI]
|
0.000146699
|
|
|
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes
|
[NCBI]
|
0.000146699
|
|
|
WGN1
|
[NCBI]
|
0.000145577
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
0.000142156
|
|
|
COFS1
|
[NCBI]
|
0.000142156
|
|
|
MAF
|
[NCBI]
|
0.000141474
|
|
|
brachycephaly, deafness, cataract, microstomia, and mental retardation
|
[NCBI]
|
0.000132776
|
|
|
lactose intolerance, congenital
|
[NCBI]
|
0.000123239
|
|
|
CRYZ
|
[NCBI]
|
0.000121803
|
|
|
GLULD1
|
[NCBI]
|
0.000121803
|
|
|
CTPP4
|
[NCBI]
|
0.000121803
|
|
|
SEC23A
|
[NCBI]
|
0.000121803
|
|
|
TNF
|
[NCBI]
|
0.000115401
|
|
|
RP
|
[NCBI]
|
0.000110787
|
|
|
foveal hypoplasia and presenile cataract syndrome
|
[NCBI]
|
0.000110036
|
|
|
NLS
|
[NCBI]
|
0.000108223
|
|
|
SIX5
|
[NCBI]
|
0.000106278
|
|
|
BFSP1
|
[NCBI]
|
0.000102843
|
|
|
RAB3GAP1
|
[NCBI]
|
0.000102843
|
|
|
FOXE3
|
[NCBI]
|
0.000102843
|
|
|
OPA3
|
[NCBI]
|
0.000102843
|
|
|
CRYGS
|
[NCBI]
|
0.000102843
|
|
|
CDPX2
|
[NCBI]
|
9.99578e-05
|
|
|
CRYM
|
[NCBI]
|
9.42849e-05
|
|
|
leiomyomatosis, esophageal and vulval, with nephropathy
|
[NCBI]
|
9.36482e-05
|
|
|
G6PD
|
[NCBI]
|
9.04866e-05
|
|
|
VEGF
|
[NCBI]
|
8.91403e-05
|
|
|
enamel hypoplasia, cataracts, and aqueductal stenosis
|
[NCBI]
|
8.87711e-05
|
|
|
cerebellar ataxia and neurosensory deafness
|
[NCBI]
|
8.87711e-05
|
|
|
CATCN2
|
[NCBI]
|
8.87711e-05
|
|
|
cataract, sutural, with punctate and cerulean opacities
|
[NCBI]
|
8.87711e-05
|
|
|
dwarfism, mental retardation, and eye abnormality
|
[NCBI]
|
8.87711e-05
|
|
|
cataract, cortical, juvenile-onset
|
[NCBI]
|
8.87711e-05
|
|
|
lipodystrophy with congenital cataracts and neurodegeneration
|
[NCBI]
|
8.87711e-05
|
|
|
ectopia pupillae
|
[NCBI]
|
8.87711e-05
|
|
|
iris pigment layer, cleavage of
|
[NCBI]
|
8.87711e-05
|
|
|
kyrle disease
|
[NCBI]
|
8.87711e-05
|
|
|
nathalie syndrome
|
[NCBI]
|
8.87711e-05
|
|
|
aniridia, microcornea, and spontaneously reabsorbed cataract
|
[NCBI]
|
8.87711e-05
|
|
|
tachycardia, hypertension, microphthalmia, and hyperglycinuria
|
[NCBI]
|
8.87711e-05
|
|
|
bowen syndrome of multiple malformations
|
[NCBI]
|
8.87711e-05
|
|
|
cataract, pulverulent, juvenile-onset
|
[NCBI]
|
8.87711e-05
|
|
|
cataract, aberrant oral frenula, and growth retardation
|
[NCBI]
|
8.87711e-05
|
|
|
cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness
|
[NCBI]
|
8.87711e-05
|
|
|
hypertrophic neuropathy and cataract
|
[NCBI]
|
8.87711e-05
|
|
|
CASS
|
[NCBI]
|
8.87711e-05
|
|
|
dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation
|
[NCBI]
|
8.87711e-05
|
|
|
premature aging syndrome, okamoto type
|
[NCBI]
|
8.87711e-05
|
|
|
cataracts, congenital, with sensorineural deafness, down syndrome-like facial appearance, short stature, and mental retardation
|
[NCBI]
|
8.87711e-05
|
|
|
hypogonadism-cataract syndrome
|
[NCBI]
|
8.87711e-05
|
|
|
spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation
|
[NCBI]
|
8.87711e-05
|
|
|
blepharoptosis, myopia, and ectopia lentis
|
[NCBI]
|
8.87711e-05
|
|
|
chorea, remitting, with nystagmus and cataract
|
[NCBI]
|
8.87711e-05
|
|
|
peters anomaly with cataract
|
[NCBI]
|
8.87711e-05
|
|
|
hydrocephalus, endocardial fibroelastosis, and cataracts
|
[NCBI]
|
8.87711e-05
|
|
|
encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts
|
[NCBI]
|
8.87711e-05
|
|
|
CATCN3
|
[NCBI]
|
8.87711e-05
|
|
|
craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation
|
[NCBI]
|
8.87711e-05
|
|
|
PSIP1
|
[NCBI]
|
7.0152e-05
|
|
|
trichomegaly
|
[NCBI]
|
6.63664e-05
|
|
|
CC
|
[NCBI]
|
6.63664e-05
|
|
|
pellagra-like syndrome
|
[NCBI]
|
6.63664e-05
|
|
|
spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia
|
[NCBI]
|
6.63664e-05
|
|
|
histiocytic dermatoarthritis
|
[NCBI]
|
6.63664e-05
|
|
|
hyperostosis frontalis interna
|
[NCBI]
|
6.63664e-05
|
|
|
cahmr syndrome
|
[NCBI]
|
6.63664e-05
|
|
|
MCOPCT3
|
[NCBI]
|
6.63664e-05
|
|
|
epiphyseal dysplasia, multiple, with myopia and conductive deafness
|
[NCBI]
|
6.63664e-05
|
|
|
mental and growth retardation with amblyopia
|
[NCBI]
|
6.63664e-05
|
|
|
PAX6
|
[NCBI]
|
6.60728e-05
|
|
|
PEDF
|
[NCBI]
|
6.23215e-05
|
|
|
BGN
|
[NCBI]
|
6.21806e-05
|
|
|
EBP
|
[NCBI]
|
6.21806e-05
|
|
|
TMEM114
|
[NCBI]
|
6.08859e-05
|
|
|
dnase2-like acid dnase
|
[NCBI]
|
6.08859e-05
|
|
|
SOLH
|
[NCBI]
|
6.08859e-05
|
|
|
retinopathy, pigmentary, and mental retardation
|
[NCBI]
|
5.79521e-05
|
|
|
MCOPS5
|
[NCBI]
|
5.79521e-05
|
|
|
arthrogryposis and ectodermal dysplasia
|
[NCBI]
|
5.79521e-05
|
|
|
genitopalatocardiac syndrome
|
[NCBI]
|
5.79521e-05
|
|
|
FDD
|
[NCBI]
|
5.79521e-05
|
|
|
MCOP3
|
[NCBI]
|
5.79521e-05
|
|
|
AOS
|
[NCBI]
|
5.69897e-05
|
|
|
AD
|
[NCBI]
|
5.61336e-05
|
|
|
FIH
|
[NCBI]
|
5.38299e-05
|
|
|
alpha-b crystallinopathy
|
[NCBI]
|
5.25117e-05
|
|
|
cardiomyopathy, congestive, with hypergonadotropic hypogonadism
|
[NCBI]
|
5.25117e-05
|
|
|
pars planitis
|
[NCBI]
|
5.25117e-05
|
|
|
CAT
|
[NCBI]
|
5.03833e-05
|
|
|
MCOP2
|
[NCBI]
|
4.84836e-05
|
|
|
aryl hydrocarbon hydroxylase inducibility
|
[NCBI]
|
4.84836e-05
|
|
|
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly
|
[NCBI]
|
4.84836e-05
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
4.7922e-05
|
|
|
PPR
|
[NCBI]
|
4.7922e-05
|
|
|
FAM126A
|
[NCBI]
|
4.71269e-05
|
|
|
RORA
|
[NCBI]
|
4.71269e-05
|
|
|
FDFT1
|
[NCBI]
|
4.71269e-05
|
|
|
CTDP1
|
[NCBI]
|
4.71269e-05
|
|
|
LSS
|
[NCBI]
|
4.71269e-05
|
|
|
SLOS
|
[NCBI]
|
4.55881e-05
|
|
|
stickler syndrome, type i, nonsyndromic ocular
|
[NCBI]
|
4.52874e-05
|
|
|
basal ganglia disease, adult-onset
|
[NCBI]
|
4.52874e-05
|
|
|
mevalonic aciduria
|
[NCBI]
|
4.52874e-05
|
|
|
AN2
|
[NCBI]
|
4.4126e-05
|
|
|
galactosemia
|
[NCBI]
|
4.29897e-05
|
|
|
CSA
|
[NCBI]
|
4.29897e-05
|
|
|
glaucoma, normal tension, susceptibility to
|
[NCBI]
|
4.26409e-05
|
|
|
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
|
[NCBI]
|
4.26409e-05
|
|
|
HDAC9
|
[NCBI]
|
4.19472e-05
|
|
|
UBE2I
|
[NCBI]
|
4.19472e-05
|
|
|
MTTS2
|
[NCBI]
|
4.19472e-05
|
|
|
LUM
|
[NCBI]
|
4.19472e-05
|
|
|
RTS
|
[NCBI]
|
4.13743e-05
|
|
|
DMPK
|
[NCBI]
|
4.05604e-05
|
|
|
AN1
|
[NCBI]
|
4.03851e-05
|
|
|
CMRD
|
[NCBI]
|
4.03851e-05
|
|
|
RP2
|
[NCBI]
|
4.01544e-05
|
|
|
FGF2
|
[NCBI]
|
3.8617e-05
|
|
|
SLC4A4
|
[NCBI]
|
3.85911e-05
|
|
|
behcet syndrome
|
[NCBI]
|
3.836e-05
|
|
|
pierson syndrome
|
[NCBI]
|
3.66844e-05
|
|
|
PCBD1
|
[NCBI]
|
3.61011e-05
|
|
|
AQP9
|
[NCBI]
|
3.61011e-05
|
|
|
ND
|
[NCBI]
|
3.57883e-05
|
|
|
SBS
|
[NCBI]
|
3.51285e-05
|
|
|
MCOPS9
|
[NCBI]
|
3.51285e-05
|
|
|
MTTH
|
[NCBI]
|
3.41212e-05
|
|
|
kindler syndrome
|
[NCBI]
|
3.37207e-05
|
|
|
schwannomatosis
|
[NCBI]
|
3.37207e-05
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
3.37207e-05
|
|
|
wagr syndrome
|
[NCBI]
|
3.37207e-05
|
|
|
LAMB2
|
[NCBI]
|
3.24784e-05
|
|
|
SIL1
|
[NCBI]
|
3.24784e-05
|
|
|
MBNL1
|
[NCBI]
|
3.24784e-05
|
|
|
KRT16
|
[NCBI]
|
3.24784e-05
|
|
|
WZS
|
[NCBI]
|
3.24361e-05
|
|
|
COL2A1
|
[NCBI]
|
3.12274e-05
|
|
|
CDS
|
[NCBI]
|
3.01649e-05
|
|
|
RHCE
|
[NCBI]
|
2.9851e-05
|
|
|
RHD
|
[NCBI]
|
2.9851e-05
|
|
|
HIP1
|
[NCBI]
|
2.9851e-05
|
|
|
marshall syndrome
|
[NCBI]
|
2.91513e-05
|
|
|
FTNS
|
[NCBI]
|
2.91513e-05
|
|
|
FGF3
|
[NCBI]
|
2.8766e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
2.82054e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
2.82054e-05
|
|
|
XFS
|
[NCBI]
|
2.82054e-05
|
|
|
galactose epimerase deficiency
|
[NCBI]
|
2.82054e-05
|
|
|
MCOPS3
|
[NCBI]
|
2.82054e-05
|
|
|
EGFR
|
[NCBI]
|
2.79607e-05
|
|
|
MVA
|
[NCBI]
|
2.73192e-05
|
|
|
ZNF9
|
[NCBI]
|
2.69088e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1
|
[NCBI]
|
2.6486e-05
|
|
|
SMMCI
|
[NCBI]
|
2.6486e-05
|
|
|
GALE
|
[NCBI]
|
2.61012e-05
|
|
|
WT1
|
[NCBI]
|
2.58247e-05
|
|
|
danon disease
|
[NCBI]
|
2.57004e-05
|
|
|
COL11A1
|
[NCBI]
|
2.53575e-05
|
|
|
ichthyosis congenita, harlequin fetus type
|
[NCBI]
|
2.49574e-05
|
|
|
AGS1
|
[NCBI]
|
2.49574e-05
|
|
|
GPX1
|
[NCBI]
|
2.40271e-05
|
|
|
MPO
|
[NCBI]
|
2.3682e-05
|
|
|
FED
|
[NCBI]
|
2.29468e-05
|
|
|
SLC40A1
|
[NCBI]
|
2.28638e-05
|
|
|
refsum disease
|
[NCBI]
|
2.23391e-05
|
|
|
LRP5
|
[NCBI]
|
2.13558e-05
|
|
|
EYA1
|
[NCBI]
|
2.13558e-05
|
|
|
MYH9
|
[NCBI]
|
2.13558e-05
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
2.12027e-05
|
|
|
SLC25A4
|
[NCBI]
|
2.0904e-05
|
|
|
ZS
|
[NCBI]
|
2.06888e-05
|
|
|
MHA
|
[NCBI]
|
2.06701e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
2.06701e-05
|
|
|
CNTF
|
[NCBI]
|
1.97521e-05
|
|
|
EBR1
|
[NCBI]
|
1.96678e-05
|
|
|
MKKS
|
[NCBI]
|
1.91952e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
1.91952e-05
|
|
|
OPA1
|
[NCBI]
|
1.87402e-05
|
|
|
FGF1
|
[NCBI]
|
1.85873e-05
|
|
|
SPARC
|
[NCBI]
|
1.85873e-05
|
|
|
MCOPS7
|
[NCBI]
|
1.83014e-05
|
|
|
EFE
|
[NCBI]
|
1.83014e-05
|
|
|
CAPN3
|
[NCBI]
|
1.79329e-05
|
|
|
GALT
|
[NCBI]
|
1.76232e-05
|
|
|
IGF1
|
[NCBI]
|
1.70352e-05
|
|
|
GSR
|
[NCBI]
|
1.67557e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
1.66914e-05
|
|
|
SEDC
|
[NCBI]
|
1.66914e-05
|
|
|
AQP1
|
[NCBI]
|
1.6485e-05
|
|
|
POAG
|
[NCBI]
|
1.63211e-05
|
|
|
MEB
|
[NCBI]
|
1.63211e-05
|
|
|
CNC1
|
[NCBI]
|
1.56147e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
1.52773e-05
|
|
|
PTH
|
[NCBI]
|
1.48007e-05
|
|
|
COH1
|
[NCBI]
|
1.46317e-05
|
|
|
OCA1A
|
[NCBI]
|
1.46317e-05
|
|
|
phenylketonuria
|
[NCBI]
|
1.2947e-05
|
|
|
NF2
|
[NCBI]
|
1.22154e-05
|
|
|
NGFB
|
[NCBI]
|
1.19818e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
1.18855e-05
|
|
|
HGF
|
[NCBI]
|
1.14188e-05
|
|
|
MTHFR
|
[NCBI]
|
1.06571e-05
|
|
|
ESR1
|
[NCBI]
|
1.02837e-05
|
|
|
RSTS
|
[NCBI]
|
9.93206e-06
|
|
|
MTTL1
|
[NCBI]
|
9.06229e-06
|
|
|
TERT
|
[NCBI]
|
9.06229e-06
|
|
|
TCOF
|
[NCBI]
|
9.00469e-06
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
8.76381e-06
|
|
|
FA
|
[NCBI]
|
8.74892e-06
|
|
|
SLPI
|
[NCBI]
|
8.47817e-06
|
|
|
OCP
|
[NCBI]
|
7.70682e-06
|
|
|
ILK
|
[NCBI]
|
7.21475e-06
|
|
|
WRN
|
[NCBI]
|
7.13085e-06
|
|
|
TS
|
[NCBI]
|
6.95386e-06
|
|
|
ALS1
|
[NCBI]
|
6.72676e-06
|
|
|
CTGF
|
[NCBI]
|
6.70527e-06
|
|
|
ATM
|
[NCBI]
|
6.70406e-06
|
|
|
FBN1
|
[NCBI]
|
6.70406e-06
|
|
|
LPL
|
[NCBI]
|
6.59897e-06
|
|
|
COMT
|
[NCBI]
|
6.10749e-06
|
|
|
CASR
|
[NCBI]
|
5.86192e-06
|
|
|
FGFR2
|
[NCBI]
|
5.13427e-06
|
|
|
APS1
|
[NCBI]
|
4.34828e-06
|
|
|
PCNA
|
[NCBI]
|
3.87628e-06
|
|
|
CDLS1
|
[NCBI]
|
3.31405e-06
|
|
|
BBS
|
[NCBI]
|
2.59938e-06
|
|
|
FGF7
|
[NCBI]
|
2.02286e-06
|
|
|
AT
|
[NCBI]
|
1.97514e-06
|
|
|
RB1
|
[NCBI]
|
1.91178e-06
|
|
|
LCAT
|
[NCBI]
|
1.82635e-06
|
|
|
EGF
|
[NCBI]
|
1.39708e-06
|
|
|
HPS
|
[NCBI]
|
1.35916e-06
|
|
|
AS
|
[NCBI]
|
9.59483e-07
|
|
|
HP
|
[NCBI]
|
6.18984e-07
|
|
|
BDNF
|
[NCBI]
|
5.3916e-07
|
|
|
SPP1
|
[NCBI]
|
4.92577e-07
|
|
|
leber optic atrophy
|
[NCBI]
|
4.66606e-07
|
|
|
GNRH1
|
[NCBI]
|
3.93394e-07
|
|
|
TTR
|
[NCBI]
|
3.16283e-07
|
|
|
CHS
|
[NCBI]
|
2.26816e-07
|
|
|
PPARA
|
[NCBI]
|
2.20249e-07
|
|
|
TF
|
[NCBI]
|
1.66764e-07
|
|
|
XDH
|
[NCBI]
|
5.79018e-08
|
|
|
PJS
|
[NCBI]
|
5.23212e-08
|
|
|
temporal arteritis
|
[NCBI]
|
1.08751e-08
|
|
|
PTK2
|
[NCBI]
|
1.75907e-09
|
|