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01 Eyelids [NCBI]

Gene


 Gene Link Information
Gain		 01
AFA [NCBI] 0.00374619
VCF [NCBI] 0.000279297
PPR [NCBI] 0.000202203
FOXL2 [NCBI] 0.0001268
FREM2 [NCBI] 2.49081e-05
TP63 [NCBI] 1.28573e-05
FGF10 [NCBI] 1.04797e-05
FOXL1 [NCBI] 7.32165e-06
FRAS1 [NCBI] 7.17815e-06
MRPS22 [NCBI] 7.05269e-06
GALNT3 [NCBI] 6.94124e-06
WNT7B [NCBI] 6.27387e-06
KIF21A [NCBI] 6.07798e-06
ECE1 [NCBI] 5.56698e-06
PHOX2A [NCBI] 5.46564e-06
MAP3K1 [NCBI] 5.12248e-06
VTN [NCBI] 5.08889e-06
SCN4A [NCBI] 5.0564e-06
APLP2 [NCBI] 4.90815e-06
FOXC1 [NCBI] 4.85453e-06
GDF5 [NCBI] 4.65422e-06
KRT5 [NCBI] 4.6331e-06
SCD [NCBI] 4.49665e-06
HTR1B [NCBI] 4.32175e-06
CYR61 [NCBI] 4.3066e-06
WNT5A [NCBI] 4.22715e-06
TWIST1 [NCBI] 4.22024e-06
PCNA [NCBI] 4.06347e-06
INHBA [NCBI] 4.06139e-06
FGFR2 [NCBI] 4.02678e-06
FGF23 [NCBI] 4.02113e-06
EDN1 [NCBI] 3.91947e-06
PAX3 [NCBI] 3.85074e-06
COMP [NCBI] 3.83195e-06
VCAN [NCBI] 3.69735e-06
CKAP4 [NCBI] 3.6933e-06
DBH [NCBI] 3.40479e-06
ATR [NCBI] 3.28058e-06
PARK2 [NCBI] 3.17043e-06
LAMB3 [NCBI] 3.03175e-06
NOG [NCBI] 2.82576e-06
SLC2A1 [NCBI] 2.7403e-06
TNFRSF11B [NCBI] 2.60902e-06
G6PD [NCBI] 2.54038e-06
PAX6 [NCBI] 2.46389e-06
CD68 [NCBI] 1.96703e-06
MS [NCBI] 1.70922e-06
EGF [NCBI] 1.68942e-06
GFAP [NCBI] 1.17486e-06
EGFR [NCBI] 1.15199e-06
TH [NCBI] 1.06582e-06
NPY [NCBI] 9.74253e-07



OMIM


 OMIM Link Information
gain		 01
BPES [NCBI] 0.00383733
palpebral coloboma-lipoma syndrome [NCBI] 0.00360146
blepharocheilodontic syndrome [NCBI] 0.00267153
hyperpigmentation of eyelids [NCBI] 0.00239361
kabuki syndrome [NCBI] 0.00187
schopf-schulz-passarge syndrome [NCBI] 0.00164186
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.00154106
fraser syndrome [NCBI] 0.00129656
marden-walker syndrome [NCBI] 0.00123304
rosselli-gulienetti syndrome [NCBI] 0.0011932
ablepharon-macrostomia syndrome [NCBI] 0.000923928
cryptophthalmos, unilateral or bilateral, isolated [NCBI] 0.000883295
OFD3 [NCBI] 0.000883295
oculootofacial dysplasia [NCBI] 0.000883295
burn-mckeown syndrome [NCBI] 0.000883295
ankyloblepharon filiforme adnatum and cleft palate [NCBI] 0.000875384
WS2B [NCBI] 0.000766997
popliteal pterygium syndrome, lethal type [NCBI] 0.000636255
acromelic frontonasal dysostosis [NCBI] 0.000592169
distichiasis [NCBI] 0.00055569
corneal dystrophy, crystalline, of schnyder [NCBI] 0.000497587
MYP2 [NCBI] 0.000473695
FOXL2 [NCBI] 0.000439024
ankyloblepharon-ectodermal defects-cleft lip/palate [NCBI] 0.000406769
PPR [NCBI] 0.000370325
blepharonasofacial malformation syndrome [NCBI] 0.000349351
lipoid proteinosis of urbach and wiethe [NCBI] 0.000312462
PPS [NCBI] 0.000281465
oculopalatoskeletal syndrome [NCBI] 0.000270914
cerebrofrontofacial syndrome [NCBI] 0.000241382
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000201015
EKD1 [NCBI] 0.000191228
SLE [NCBI] 0.000185564
feingold syndrome [NCBI] 0.000183236
MOTA [NCBI] 0.000174543
fraser-like syndrome [NCBI] 0.000174543
mandibulofacial dysostosis with macroblepharon and macrostomia [NCBI] 0.000174543
levator-medial rectus synkinesis [NCBI] 0.000174543
blepharochalasis, superior [NCBI] 0.000174543
MEN2B [NCBI] 0.000166205
OPMD [NCBI] 0.000147544
SJS1 [NCBI] 0.00014475
OAFNS [NCBI] 0.000135326
chands [NCBI] 0.000135326
aniridia, partial, with unilateral renal agenesis and psychomotor retardation [NCBI] 0.000135326
holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate [NCBI] 0.000135326
HFM [NCBI] 0.000130731
WS1 [NCBI] 0.000129483
carnevale syndrome [NCBI] 0.00012056
OCP [NCBI] 0.000120076
NS1 [NCBI] 0.000117675
pseudohyperkalemia cardiff [NCBI] 0.000110992
native american myopathy [NCBI] 0.000110992
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly [NCBI] 0.000103893
donnai-barrow syndrome [NCBI] 9.82479e-05
WS2A [NCBI] 8.95615e-05
oculocerebrocutaneous syndrome [NCBI] 8.29753e-05
amyloidosis v [NCBI] 8.01969e-05
NCIE1 [NCBI] 7.76773e-05
SCCMS [NCBI] 7.76773e-05
COFS1 [NCBI] 7.32511e-05
FGF10 [NCBI] 7.04563e-05
graves disease [NCBI] 6.94547e-05
HFTC [NCBI] 6.31869e-05
lymphedema-distichiasis syndrome [NCBI] 6.05392e-05
cardiofaciocutaneous syndrome [NCBI] 5.93106e-05
DA2A [NCBI] 5.49124e-05
FREM2 [NCBI] 4.95533e-05
MRPS22 [NCBI] 4.95533e-05
LI1 [NCBI] 4.79142e-05
SHH [NCBI] 4.6674e-05
GALNT3 [NCBI] 4.26348e-05
MAP3K1 [NCBI] 4.26348e-05
VANGL2 [NCBI] 4.16036e-05
ED1 [NCBI] 4.01725e-05
MAPK9 [NCBI] 3.63801e-05
MAPK8 [NCBI] 3.40295e-05
CES [NCBI] 3.39632e-05
ESR2 [NCBI] 3.12894e-05
FGF23 [NCBI] 3.06374e-05
PAX3 [NCBI] 2.79106e-05
BBS [NCBI] 2.6652e-05
ESR1 [NCBI] 2.63881e-05
SCD [NCBI] 2.41563e-05
ichthyosis, x-linked [NCBI] 2.40736e-05
FGFR2 [NCBI] 2.30793e-05
COMP [NCBI] 1.79704e-05
WBS [NCBI] 1.43146e-05
PCNA [NCBI] 1.1776e-05
MG [NCBI] 9.87069e-06
G6PD [NCBI] 8.0608e-06
EGF [NCBI] 3.99793e-06
EGFR [NCBI] 1.89753e-06
GFAP [NCBI] 1.25043e-06
TH [NCBI] 8.28203e-07
NPY [NCBI] 5.33436e-07



Database Center for Life Science