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01 Cataract [NCBI]


Gene


Gene Link Information
Gain
01
MIP [NCBI] 0.000657502
CTAA1 [NCBI] 0.0006491
ASMD [NCBI] 0.000527659
CCNP [NCBI] 0.000323455
CRYZP1 [NCBI] 0.000323455
CCV [NCBI] 0.000323455
SPG9 [NCBI] 0.000323455
CRYGEP1 [NCBI] 0.000323455
LOC619404 [NCBI] 0.000323455
CCPSO [NCBI] 0.000323455
ARCC1 [NCBI] 0.000323455
CCA1 [NCBI] 0.000323455
CTPL1 [NCBI] 0.000323455
CRYAA [NCBI] 0.000276382
CRYGD [NCBI] 0.000272536
CRYBB2P1 [NCBI] 0.000262735
CTAA2 [NCBI] 0.000262735
NNO1 [NCBI] 0.000262735
SCAR2 [NCBI] 0.000239834
NHS [NCBI] 0.00020928
MS [NCBI] 0.000188684
PAX6 [NCBI] 0.000187796
FTL [NCBI] 0.000158189
GJA3 [NCBI] 0.00014245
CRYBA1 [NCBI] 0.00014245
CRYGC [NCBI] 0.000130015
CRYBB2 [NCBI] 0.000127109
GJA8 [NCBI] 0.00012689
CRYBB1 [NCBI] 0.000121136
PPR [NCBI] 0.000117473
CRYAB [NCBI] 8.73826e-05
BFSP2 [NCBI] 8.36131e-05
CRYGS [NCBI] 8.36131e-05
TGFB2 [NCBI] 7.46612e-05
PITX3 [NCBI] 6.837e-05
NEWENTRY [NCBI] 6.78364e-05
CRYBB3 [NCBI] 6.34034e-05
HSF4 [NCBI] 6.30847e-05
CRYGB [NCBI] 5.43185e-05
CRYBA4 [NCBI] 5.2791e-05
MAF [NCBI] 4.73773e-05
GALK1 [NCBI] 4.7019e-05
MYH9 [NCBI] 3.85678e-05
LIM2 [NCBI] 3.80322e-05
OCRL [NCBI] 3.45242e-05
GCNT2 [NCBI] 3.41707e-05
FAM126A [NCBI] 2.98277e-05
SIL1 [NCBI] 2.59837e-05
SORD [NCBI] 2.53515e-05
OPA3 [NCBI] 2.51558e-05
DMPK [NCBI] 2.488e-05
CTDP1 [NCBI] 2.20736e-05
RAI2 [NCBI] 2.20736e-05
SIX5 [NCBI] 2.16873e-05
TGFBI [NCBI] 2.14757e-05
EBP [NCBI] 2.09667e-05
SEC23A [NCBI] 2.05926e-05
BFSP1 [NCBI] 2.05926e-05
RAB3GAP1 [NCBI] 2.05926e-05
SERPINF1 [NCBI] 2.05659e-05
TGFB1 [NCBI] 2.03986e-05
CAT [NCBI] 2.01879e-05
G6PD [NCBI] 1.97221e-05
CRYGA [NCBI] 1.95763e-05
DNASE2B [NCBI] 1.9391e-05
COL2A1 [NCBI] 1.88907e-05
GALT [NCBI] 1.74687e-05
FOXE3 [NCBI] 1.71726e-05
SLC5A3 [NCBI] 1.30072e-05
BGN [NCBI] 1.28833e-05
CDKL5 [NCBI] 1.27638e-05
SLC16A12 [NCBI] 1.26741e-05
MRGPRX3 [NCBI] 1.26741e-05
NHSL1 [NCBI] 1.26741e-05
TMEM114 [NCBI] 1.26741e-05
EGF [NCBI] 1.23878e-05
PCNA [NCBI] 1.06437e-05
SPARC [NCBI] 1.05321e-05
LGR4 [NCBI] 1.02947e-05
DMBX1 [NCBI] 1.02947e-05
LYPLAL1 [NCBI] 1.02947e-05
SOLH [NCBI] 1.02947e-05
CAPN9 [NCBI] 1.02947e-05
CAPN8 [NCBI] 1.02947e-05
DNASE2 [NCBI] 1.02947e-05
SOX2 [NCBI] 9.92788e-06
OCA2 [NCBI] 9.59405e-06
ODF1 [NCBI] 9.39724e-06
MAFF [NCBI] 9.39724e-06
LGSN [NCBI] 9.39724e-06
GPR161 [NCBI] 9.39724e-06
LENEP [NCBI] 9.39724e-06
RHOJ [NCBI] 9.39724e-06
MMP23B [NCBI] 9.39724e-06
CHMP4B [NCBI] 9.39724e-06
SIX4 [NCBI] 9.39724e-06
CLCN1 [NCBI] 9.12981e-06
CNTF [NCBI] 8.92252e-06
COL12A1 [NCBI] 8.81482e-06
ALDH18A1 [NCBI] 8.81482e-06
CRYZ [NCBI] 8.81482e-06
CAPNS1 [NCBI] 8.81482e-06
DPP3 [NCBI] 8.382e-06
MAN2C1 [NCBI] 8.382e-06
LSS [NCBI] 8.03731e-06
REPS2 [NCBI] 8.03731e-06
SYNC [NCBI] 8.03731e-06
PPEF1 [NCBI] 8.03731e-06
CTDSP1 [NCBI] 7.75085e-06
GNPAT [NCBI] 7.50576e-06
PYCR1 [NCBI] 7.29162e-06
CYP27A1 [NCBI] 7.27039e-06
NAT2 [NCBI] 7.19286e-06
SIX6 [NCBI] 7.1015e-06
MAFB [NCBI] 7.1015e-06
ADAM2 [NCBI] 7.1015e-06
SOX1 [NCBI] 6.93057e-06
HDAC9 [NCBI] 6.93057e-06
RPL21 [NCBI] 6.93057e-06
KHK [NCBI] 6.77531e-06
GPX1 [NCBI] 6.74576e-06
LUM [NCBI] 6.50197e-06
HSPB2 [NCBI] 6.38028e-06
NRCAM [NCBI] 5.96608e-06
KLC1 [NCBI] 5.87673e-06
GALE [NCBI] 5.87673e-06
KRT16 [NCBI] 5.79191e-06
RBBP7 [NCBI] 5.79191e-06
ANK2 [NCBI] 5.71118e-06
HFE [NCBI] 5.65142e-06
SNAI2 [NCBI] 5.63913e-06
PCBD1 [NCBI] 5.63417e-06
OTX2 [NCBI] 5.63417e-06
KCNN3 [NCBI] 5.56055e-06
SEPN1 [NCBI] 5.56055e-06
RHD [NCBI] 5.49005e-06
GSTT2 [NCBI] 5.49005e-06
SKIL [NCBI] 5.42242e-06
SIX1 [NCBI] 5.42242e-06
FAT1 [NCBI] 5.42242e-06
TJP1 [NCBI] 5.35791e-06
NR2E3 [NCBI] 5.35742e-06
TNFSF15 [NCBI] 5.35742e-06
MYOC [NCBI] 5.31167e-06
MSRA [NCBI] 5.29488e-06
RHCE [NCBI] 5.23461e-06
CAPN1 [NCBI] 5.12027e-06
ALOX12 [NCBI] 5.12027e-06
AIPL1 [NCBI] 5.06594e-06
PHYH [NCBI] 5.06594e-06
ITM2B [NCBI] 5.01334e-06
CUGBP1 [NCBI] 5.01334e-06
CNBP [NCBI] 4.91292e-06
ADAM9 [NCBI] 4.86492e-06
MYOT [NCBI] 4.86492e-06
DPP7 [NCBI] 4.86492e-06
LOXL1 [NCBI] 4.81829e-06
DPEP1 [NCBI] 4.77294e-06
GSR [NCBI] 4.77294e-06
TP53BP2 [NCBI] 4.77294e-06
PRDX1 [NCBI] 4.77294e-06
HSPB8 [NCBI] 4.72882e-06
GSTM1 [NCBI] 4.56157e-06
SLC40A1 [NCBI] 4.48652e-06
EPHA2 [NCBI] 4.44943e-06
HIP1 [NCBI] 4.44943e-06
LCT [NCBI] 4.44943e-06
UBE2I [NCBI] 4.41316e-06
TGFB3 [NCBI] 4.41316e-06
TNF [NCBI] 4.40291e-06
TGFBR1 [NCBI] 4.32568e-06
LAMP2 [NCBI] 4.30901e-06
HTRA1 [NCBI] 4.24313e-06
ERCC2 [NCBI] 4.2154e-06
OAT [NCBI] 4.14911e-06
PAX7 [NCBI] 4.0603e-06
PITX1 [NCBI] 3.97618e-06
DARC [NCBI] 3.89628e-06
EYA1 [NCBI] 3.89628e-06
BMP6 [NCBI] 3.84517e-06
LAMA1 [NCBI] 3.70107e-06
NEFM [NCBI] 3.56912e-06
CAPN10 [NCBI] 3.54817e-06
BEST1 [NCBI] 3.4671e-06
MSN [NCBI] 3.44748e-06
NF2 [NCBI] 3.40898e-06
CAPN3 [NCBI] 3.26394e-06
RS1 [NCBI] 3.24674e-06
COMT [NCBI] 3.09722e-06
ERCC6 [NCBI] 3.02448e-06
TGM2 [NCBI] 2.96659e-06
ILK [NCBI] 2.92461e-06
CTGF [NCBI] 2.92183e-06
SCARB1 [NCBI] 2.85718e-06
GATA3 [NCBI] 2.81816e-06
PXN [NCBI] 2.69516e-06
KRT14 [NCBI] 2.50752e-06
SLPI [NCBI] 2.46675e-06
GSTT1 [NCBI] 2.44418e-06
ATP7A [NCBI] 2.41741e-06
FGF2 [NCBI] 2.36041e-06
RAD9A [NCBI] 2.34192e-06
CASR [NCBI] 2.34192e-06
IL13 [NCBI] 2.21069e-06
NEFL [NCBI] 2.19411e-06
SAT2 [NCBI] 2.1859e-06
AQP2 [NCBI] 2.12195e-06
NAT1 [NCBI] 2.0911e-06
MITF [NCBI] 2.04612e-06
BMP4 [NCBI] 1.88685e-06
SMAD2 [NCBI] 1.75706e-06
RB1 [NCBI] 1.74537e-06
LMNA [NCBI] 1.69415e-06
MAP2K1 [NCBI] 1.51833e-06
HSPB1 [NCBI] 1.50877e-06
PDGFA [NCBI] 1.4485e-06
CASP3 [NCBI] 1.43361e-06
CLU [NCBI] 1.42173e-06
SLC11A1 [NCBI] 1.39991e-06
BAX [NCBI] 1.33991e-06
HNF1B [NCBI] 1.25076e-06
TERT [NCBI] 1.23583e-06
XRCC1 [NCBI] 1.23213e-06
BDNF [NCBI] 1.23203e-06
HP [NCBI] 1.22477e-06
HNF1A [NCBI] 1.13699e-06
CDKN1B [NCBI] 1.10394e-06
MTHFR [NCBI] 1.03706e-06
TF [NCBI] 1.02296e-06
MMP2 [NCBI] 9.65115e-07
PON1 [NCBI] 8.42432e-07
TTR [NCBI] 7.52782e-07
IFNGR1 [NCBI] 7.06418e-07
PTH [NCBI] 6.76578e-07
GJB2 [NCBI] 5.33575e-07
CDK2 [NCBI] 4.90843e-07
APOE [NCBI] 3.32698e-07
FASLG [NCBI] 1.88402e-07
CASP9 [NCBI] 1.83659e-07
NGF [NCBI] 1.67978e-07
MPO [NCBI] 1.40857e-07
EPO [NCBI] 1.27556e-07
VEGFA [NCBI] 1.09805e-07
SOD1 [NCBI] 9.90851e-08
EGFR [NCBI] 9.60878e-08
BCL2L1 [NCBI] 6.22096e-08
LPL [NCBI] 3.55936e-08
CD68 [NCBI] 1.4069e-08
CDKN1A [NCBI] 1.04657e-08
PTEN [NCBI] 6.11296e-09
HGF [NCBI] 8.08611e-10
NOS2 [NCBI] 6.00517e-11




OMIM


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




Database Center for Life Science