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01 Pterygium [NCBI]

Gene


 Gene Link Information
Gain		 01
PROM1 [NCBI] 2.99414e-05
VEGFA [NCBI] 2.88155e-05
TFF3 [NCBI] 2.83176e-05
IRF6 [NCBI] 1.79451e-05
PCNA [NCBI] 1.57553e-05
TFF2 [NCBI] 1.44461e-05
EGFR [NCBI] 1.31353e-05
SERPINF1 [NCBI] 1.3093e-05
STAG1 [NCBI] 1.24282e-05
TFF1 [NCBI] 1.1374e-05
TPSAB1 [NCBI] 1.08147e-05
TP53 [NCBI] 1.07795e-05
BST1 [NCBI] 1.00941e-05
ACAT1 [NCBI] 1.00941e-05
XRCC6 [NCBI] 8.38223e-06
CCL26 [NCBI] 8.34655e-06
MUC5AC [NCBI] 8.31161e-06
POSTN [NCBI] 8.21087e-06
LEF1 [NCBI] 8.05515e-06
CCL18 [NCBI] 7.96811e-06
DNMT3B [NCBI] 7.63518e-06
EPOR [NCBI] 6.72165e-06
MMP7 [NCBI] 6.49331e-06
OGG1 [NCBI] 6.28169e-06
LCN2 [NCBI] 6.09371e-06
SNAI2 [NCBI] 5.56773e-06
CKAP4 [NCBI] 5.3501e-06
ICAM1 [NCBI] 5.24547e-06
CDKN1A [NCBI] 4.78134e-06
TP63 [NCBI] 4.63167e-06
MUC1 [NCBI] 4.31858e-06
CTGF [NCBI] 4.05373e-06
CDKN2A [NCBI] 4.03485e-06
IL1B [NCBI] 3.6722e-06
GSTM1 [NCBI] 3.45565e-06
MLH1 [NCBI] 2.56268e-06
IL1RN [NCBI] 2.53347e-06
NOS2 [NCBI] 2.50875e-06
TGFB1 [NCBI] 2.10817e-06
BAX [NCBI] 2.06498e-06
VWF [NCBI] 2.01563e-06
PTGS2 [NCBI] 1.17069e-06
EGF [NCBI] 1.062e-06
TNF [NCBI] 3.43811e-07



OMIM


 OMIM Link Information
gain		 01
pena-shokeir syndrome, type i [NCBI] 0.00192987
popliteal pterygium syndrome, lethal type [NCBI] 0.00165826
pterygium of conjunctiva and cornea [NCBI] 0.000781106
DA5 [NCBI] 0.000656414
gordon syndrome [NCBI] 0.000656414
PPS [NCBI] 0.000557863
pterygia, mental retardation, and distinctive craniofacial features [NCBI] 0.000477918
multiple pterygium syndrome, escobar variant [NCBI] 0.000377517
multiple pterygium syndrome, lethal type [NCBI] 0.000274245
pterygium syndrome, multiple, x-linked [NCBI] 0.000227206
spondylospinal thoracic dysostosis [NCBI] 0.000128816
VEGF [NCBI] 0.000127908
pterygium colli and mental retardation with facial and digital anomalies [NCBI] 0.000106349
contractures, congenital, torticollis, and malignant hyperthermia [NCBI] 0.000106349
lymphedema and ptosis [NCBI] 0.000106349
pterygium syndrome, multiple, autosomal dominant [NCBI] 0.000106349
chands [NCBI] 9.78725e-05
mental retardation with epilepsy and characteristic facies [NCBI] 9.23698e-05
EGFR [NCBI] 6.30645e-05
lymphedema-distichiasis syndrome [NCBI] 6.29905e-05
DNMT3B [NCBI] 4.91925e-05
MHS1 [NCBI] 4.64383e-05
PCNA [NCBI] 4.51559e-05
AMC [NCBI] 4.44702e-05
NPS [NCBI] 4.44702e-05
PEDF [NCBI] 3.10195e-05
CTGF [NCBI] 2.29965e-05
EGF [NCBI] 2.31697e-06



Database Center for Life Science