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MeSH keywords -> Related genes, diseases (OMIM)


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01 Microphthalmos [NCBI]


Gene


Gene Link Information
Gain
01
MOPCB1 [NCBI] 0.000401057
WS2A [NCBI] 0.000401057
MOPCB2 [NCBI] 0.000401057
WS2B [NCBI] 0.000401057
SOX2OT [NCBI] 0.000401057
MITF [NCBI] 0.000153727
PAX6 [NCBI] 0.000132019
HCCS [NCBI] 8.82756e-05
MFRP [NCBI] 7.67892e-05
VSX2 [NCBI] 6.70113e-05
SOX2 [NCBI] 5.83696e-05
ARHGAP6 [NCBI] 5.77709e-05
NHS [NCBI] 3.26011e-05
DCT [NCBI] 2.80346e-05
SIX6 [NCBI] 2.24081e-05
BCOR [NCBI] 2.20451e-05
OTX2 [NCBI] 1.93351e-05
CRYAA [NCBI] 1.88965e-05
SIX3 [NCBI] 1.78419e-05
PITX3 [NCBI] 1.54679e-05
DMBX1 [NCBI] 1.31108e-05
SOLH [NCBI] 1.31108e-05
TYRP1 [NCBI] 1.31012e-05
MAFF [NCBI] 1.22125e-05
LIM2 [NCBI] 1.22125e-05
RAI2 [NCBI] 1.22125e-05
RAB3GAP1 [NCBI] 1.16292e-05
KLF13 [NCBI] 1.16292e-05
SNX3 [NCBI] 1.16292e-05
TFEC [NCBI] 1.11955e-05
RPP30 [NCBI] 1.11955e-05
STRA6 [NCBI] 1.11955e-05
CLCN4 [NCBI] 1.085e-05
NR2E1 [NCBI] 1.05627e-05
CRYBA4 [NCBI] 1.01017e-05
CDH4 [NCBI] 8.96364e-06
TBCE [NCBI] 8.76754e-06
MID1 [NCBI] 8.51005e-06
E2F2 [NCBI] 8.3577e-06
FAT1 [NCBI] 8.21783e-06
CDKL5 [NCBI] 7.96842e-06
USF2 [NCBI] 7.91138e-06
GREM1 [NCBI] 7.65171e-06
TGIF1 [NCBI] 7.60421e-06
FGF10 [NCBI] 7.22759e-06
UBE2I [NCBI] 7.19046e-06
E2F4 [NCBI] 6.82811e-06
NTN1 [NCBI] 6.74139e-06
MIP [NCBI] 6.65891e-06
FOXC1 [NCBI] 6.43315e-06
TFE3 [NCBI] 6.36415e-06
BEST1 [NCBI] 6.21334e-06
AVP [NCBI] 5.55975e-06
PAX5 [NCBI] 5.32313e-06
NOG [NCBI] 5.27541e-06
SPI1 [NCBI] 5.0148e-06
PTPN6 [NCBI] 4.99484e-06
IGFBP3 [NCBI] 4.20081e-06
BMP7 [NCBI] 4.14688e-06
ARID4A [NCBI] 4.11768e-06
MAP2K1 [NCBI] 4.08332e-06
SLC11A1 [NCBI] 3.94246e-06
SHH [NCBI] 3.87149e-06
BTK [NCBI] 3.69795e-06
E2F1 [NCBI] 3.52573e-06
ACP5 [NCBI] 2.89333e-06
CDK4 [NCBI] 2.77266e-06
TNFRSF11A [NCBI] 2.76544e-06
TNFSF11 [NCBI] 2.54539e-06
G6PD [NCBI] 2.32645e-06
NPY [NCBI] 1.46409e-06




OMIM


OMIM Link Information
gain
01
MCOPS1 [NCBI] 0.00504731
MCOP1 [NCBI] 0.00330266
NNO1 [NCBI] 0.00290322
MCOPS7 [NCBI] 0.00247159
MCOPCB2 [NCBI] 0.00174232
kenny-caffey syndrome, type 2 [NCBI] 0.00161141
persistent hyperplastic primary vitreous, autosomal recessive [NCBI] 0.0013076
MCOPS4 [NCBI] 0.0013076
RNANC [NCBI] 0.00108688
MCOPCB1 [NCBI] 0.000868983
MCOPS10 [NCBI] 0.000868983
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000846808
lymphedema, microcephaly, chorioretinopathy syndrome [NCBI] 0.000802936
MCOPCT1 [NCBI] 0.000651642
WS2B [NCBI] 0.000569992
MCOPS9 [NCBI] 0.00053211
oculodentoosseous dysplasia, recessive [NCBI] 0.000517186
MITF [NCBI] 0.000483879
CCA1 [NCBI] 0.000447038
acromelic frontonasal dysostosis [NCBI] 0.000447038
MCOPS6 [NCBI] 0.00042133
MCOPS2 [NCBI] 0.000397603
MCOP2 [NCBI] 0.000395432
ODDD [NCBI] 0.000392502
HYPX [NCBI] 0.000380325
NHS [NCBI] 0.000363316
MCOPCB3 [NCBI] 0.000326751
MCOPS3 [NCBI] 0.000285866
CHX10 [NCBI] 0.000273192
WARBM [NCBI] 0.000241053
NLS [NCBI] 0.000218042
MCOPCB4 [NCBI] 0.000217683
GJA8 [NCBI] 0.000214002
HCCS [NCBI] 0.000210747
coloboma, uveal, with cleft lip and palate and mental retardation [NCBI] 0.000186748
moved to 310600 [NCBI] 0.000186748
gombo syndrome [NCBI] 0.000172777
GJA3 [NCBI] 0.000166058
MLRD [NCBI] 0.000163192
ARHGAP6 [NCBI] 0.000155232
coloboma, ocular [NCBI] 0.000136721
HRD [NCBI] 0.000133312
KCS [NCBI] 0.000133312
BCOR [NCBI] 0.000127678
WS2A [NCBI] 0.000124842
MFRP [NCBI] 0.000117283
NHS [NCBI] 0.000113621
tachycardia, hypertension, microphthalmia, and hyperglycinuria [NCBI] 0.000108767
retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma [NCBI] 0.000108767
retinal nonattachment and falciform detachment [NCBI] 0.000108767
microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen [NCBI] 0.000108767
macrosomia with microphthalmia, lethal [NCBI] 0.000108767
SOX2 [NCBI] 9.53617e-05
walker-warburg syndrome [NCBI] 8.89011e-05
microphthalmia, isolated, with cataract 4 [NCBI] 8.63138e-05
NNO2 [NCBI] 8.63138e-05
teebi-shaltout syndrome [NCBI] 8.63138e-05
dextrocardia with unusual facies and microphthalmia [NCBI] 8.63138e-05
cataract, lamellar 2 [NCBI] 8.63138e-05
AN2 [NCBI] 8.18604e-05
CES [NCBI] 8.12378e-05
MCOP3 [NCBI] 7.78513e-05
arhinia, choanal atresia, and microphthalmia [NCBI] 7.78513e-05
coloboma of optic nerve [NCBI] 7.78513e-05
MCOPS5 [NCBI] 7.78513e-05
yemenite deaf-blind hypopigmentation syndrome [NCBI] 7.78513e-05
CLCN4 [NCBI] 7.75317e-05
SOLH [NCBI] 7.75317e-05
MCOPS8 [NCBI] 7.23626e-05
fryns microphthalmia syndrome [NCBI] 7.23626e-05
PAX6 [NCBI] 6.86314e-05
jejunal atresia with microcephaly and ocular anomalies [NCBI] 6.82864e-05
CTPP4 [NCBI] 6.3755e-05
CCA2 [NCBI] 6.23472e-05
SNX3 [NCBI] 5.85576e-05
UBE2I [NCBI] 5.85576e-05
STRA6 [NCBI] 5.85576e-05
IRID1 [NCBI] 5.46419e-05
wagr syndrome [NCBI] 5.31859e-05
oculocerebrocutaneous syndrome [NCBI] 5.31859e-05
CCT [NCBI] 5.26761e-05
RENS1 [NCBI] 5.18531e-05
CRYBA4 [NCBI] 5.06786e-05
TFAP2A [NCBI] 4.90181e-05
COFS1 [NCBI] 4.84236e-05
GJA1 [NCBI] 4.80384e-05
SMMCI [NCBI] 4.56137e-05
AIED [NCBI] 4.47798e-05
MSX2 [NCBI] 4.42609e-05
PITX3 [NCBI] 4.42609e-05
AGS1 [NCBI] 4.39886e-05
RB1 [NCBI] 4.20909e-05
PQBP1 [NCBI] 3.97898e-05
OPTB1 [NCBI] 3.93636e-05
RIEG1 [NCBI] 3.93636e-05
BOR1 [NCBI] 3.72408e-05
SOX10 [NCBI] 3.58917e-05
FIH [NCBI] 3.49508e-05
charge syndrome [NCBI] 3.45323e-05
PIGA [NCBI] 3.25292e-05
ACP5 [NCBI] 3.22526e-05
PHS [NCBI] 3.22444e-05
FDH [NCBI] 3.18956e-05
VMD [NCBI] 3.18956e-05
KIT [NCBI] 3.17124e-05
FANCA [NCBI] 3.14548e-05
MKS1 [NCBI] 2.7482e-05
PAX3 [NCBI] 2.70505e-05
IP [NCBI] 1.55387e-05
TP53 [NCBI] 1.46794e-05
DGS [NCBI] 1.18071e-05
SHH [NCBI] 1.13165e-05
VEGF [NCBI] 1.05281e-05
AVP [NCBI] 7.676e-06
G6PD [NCBI] 2.98e-06
FA [NCBI] 8.80678e-07
NPY [NCBI] 8.41416e-07
RP [NCBI] 2.53815e-07




Database Center for Life Science