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01 Anterior Eye Segment [NCBI]

Gene


 Gene Link Information
Gain		 01
ASMD [NCBI] 0.00157759
FOXC1 [NCBI] 0.000232025
PITX2 [NCBI] 6.4488e-05
PAX6 [NCBI] 6.387e-05
CYP1B1 [NCBI] 3.65996e-05
PITX3 [NCBI] 2.70262e-05
FOXE3 [NCBI] 2.23875e-05
MYOC [NCBI] 1.85442e-05
OPTN [NCBI] 1.7607e-05
FOXC2 [NCBI] 1.65789e-05
PITX1 [NCBI] 1.37294e-05
VEGFA [NCBI] 9.10251e-06
TGFBI [NCBI] 7.85214e-06
LGR4 [NCBI] 7.35128e-06
WDR36 [NCBI] 6.24863e-06
TGFBR1 [NCBI] 5.75823e-06
PDCD1LG2 [NCBI] 5.18189e-06
COCH [NCBI] 4.87424e-06
SDC3 [NCBI] 4.69826e-06
COL4A1 [NCBI] 4.48172e-06
MAF [NCBI] 4.44981e-06
CD68 [NCBI] 4.13674e-06
SDC2 [NCBI] 4.07511e-06
HSD11B2 [NCBI] 3.92565e-06
TSC2 [NCBI] 3.83727e-06
SDC4 [NCBI] 3.79588e-06
NOTCH3 [NCBI] 3.65982e-06
LAMA1 [NCBI] 3.55292e-06
CD274 [NCBI] 3.53411e-06
PAX2 [NCBI] 3.52177e-06
GJA1 [NCBI] 3.42827e-06
C1QBP [NCBI] 3.25044e-06
TGFB1 [NCBI] 3.14831e-06
CBX4 [NCBI] 2.99474e-06
TGFB2 [NCBI] 2.95972e-06
DBH [NCBI] 2.82217e-06
NME1 [NCBI] 2.75876e-06
SDC1 [NCBI] 2.74217e-06
CLU [NCBI] 2.72049e-06
VIP [NCBI] 2.69869e-06
JAG1 [NCBI] 2.58817e-06
NOTCH1 [NCBI] 2.57199e-06
CNN1 [NCBI] 2.56742e-06
BMP7 [NCBI] 2.42197e-06
TH [NCBI] 2.31519e-06
BMP4 [NCBI] 2.30297e-06
NPY [NCBI] 2.12862e-06
TJP1 [NCBI] 1.76781e-06
IL1RN [NCBI] 1.63035e-06
NOS2 [NCBI] 1.18601e-06
MPO [NCBI] 9.59438e-07
TNF [NCBI] 8.96275e-07
BDNF [NCBI] 8.2407e-07
EGF [NCBI] 8.08578e-07
ACHE [NCBI] 6.58018e-07



OMIM


 OMIM Link Information
gain		 01
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss [NCBI] 0.00454984
glaucoma-related pigment dispersion syndrome [NCBI] 0.00179198
persistent hyperplastic primary vitreous, autosomal recessive [NCBI] 0.000983418
ASMD [NCBI] 0.000856643
megalocornea-mental retardation syndrome [NCBI] 0.000760427
al-gazali syndrome [NCBI] 0.000371241
peters anomaly [NCBI] 0.000330033
XFS [NCBI] 0.000277694
FOXC1 [NCBI] 0.000234323
VRNI [NCBI] 0.000224639
RIEG1 [NCBI] 0.000221585
cataract, pulverulent, juvenile-onset [NCBI] 0.000212159
AN2 [NCBI] 0.00019416
PITX2 [NCBI] 0.000164279
HANAC [NCBI] 0.000158087
IP [NCBI] 0.000147386
RP [NCBI] 0.000137749
cataract-microcornea syndrome [NCBI] 0.000126869
IRID2 [NCBI] 0.000117372
wagr syndrome [NCBI] 0.000117372
PAX6 [NCBI] 9.87811e-05
NS1 [NCBI] 7.57621e-05
OPTN [NCBI] 7.50752e-05
osteogenesis imperfecta, type i [NCBI] 7.03991e-05
MAF [NCBI] 4.15426e-05
PITX3 [NCBI] 3.88096e-05
CYP1B1 [NCBI] 3.88096e-05
FOXC2 [NCBI] 3.48403e-05
temporal arteritis [NCBI] 3.46091e-05
ADORA3 [NCBI] 3.06715e-05
homocystinuria [NCBI] 2.66863e-05
ENPEP [NCBI] 2.60252e-05
COL1A1 [NCBI] 2.57772e-05
MYOC [NCBI] 2.54208e-05
CLU [NCBI] 2.41522e-05
PTGS2 [NCBI] 2.30782e-05
SLE [NCBI] 1.83482e-05
SLC18A3 [NCBI] 1.72251e-05
VEGF [NCBI] 1.18959e-05
VIP [NCBI] 8.21519e-06
TH [NCBI] 6.01451e-06
NPY [NCBI] 5.00111e-06
MPO [NCBI] 1.95983e-06
BDNF [NCBI] 1.37696e-06
ACHE [NCBI] 6.72095e-07
TNF [NCBI] 4.39893e-07
EGF [NCBI] 6.95817e-08



Database Center for Life Science