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MeSH keywords -> Related genes, diseases (OMIM)


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01 Lymphedema [NCBI]

Gene


 Gene Link Information
Gain		 01
FOXC2 [NCBI] 0.000468085
LCS1 [NCBI] 0.000415947
LGMD1D [NCBI] 0.000332278
NEWENTRY [NCBI] 0.000157063
FLT4 [NCBI] 0.00010877
SOX18 [NCBI] 5.48729e-05
FOXL1 [NCBI] 2.83889e-05
PROX1 [NCBI] 2.32916e-05
FIGF [NCBI] 2.07804e-05
FOXC1 [NCBI] 1.74161e-05
EMILIN1 [NCBI] 1.6559e-05
VEGFC [NCBI] 1.55824e-05
FOXJ2 [NCBI] 1.32802e-05
HNRNPH1 [NCBI] 1.26968e-05
RORC [NCBI] 1.26968e-05
IKBKE [NCBI] 1.25737e-05
FOXF1 [NCBI] 1.2263e-05
CHUK [NCBI] 1.22258e-05
IKBKB [NCBI] 1.22052e-05
LCP2 [NCBI] 1.16299e-05
FOXI1 [NCBI] 1.16299e-05
SOX17 [NCBI] 1.16299e-05
CCR9 [NCBI] 1.11688e-05
CMKLR1 [NCBI] 1.09777e-05
LYVE1 [NCBI] 1.08058e-05
NRP2 [NCBI] 9.74336e-06
VEGFB [NCBI] 9.28329e-06
PDPN [NCBI] 9.15383e-06
FABP4 [NCBI] 9.15383e-06
TEC [NCBI] 8.92106e-06
NAGA [NCBI] 7.89049e-06
SYK [NCBI] 7.86099e-06
TYK2 [NCBI] 7.49409e-06
ANGPT2 [NCBI] 7.29414e-06
CCL21 [NCBI] 6.88622e-06
HGF [NCBI] 6.8273e-06
FOXO3 [NCBI] 6.77461e-06
VCAM1 [NCBI] 6.65547e-06
SHOX [NCBI] 6.57131e-06
KDR [NCBI] 6.47816e-06
MET [NCBI] 5.54007e-06
SMAD3 [NCBI] 5.35789e-06
NPHS1 [NCBI] 5.2801e-06
PTPN11 [NCBI] 4.86257e-06
PTHLH [NCBI] 3.2957e-06
CD68 [NCBI] 2.54956e-06



OMIM


 OMIM Link Information
gain		 01
lymphedema, microcephaly, chorioretinopathy syndrome [NCBI] 0.00999221
hennekam lymphangiectasia-lymphedema syndrome [NCBI] 0.00486634
cholestasis-lymphedema syndrome [NCBI] 0.00420327
lymphedema-distichiasis syndrome [NCBI] 0.00197776
lymphedema, hereditary, i [NCBI] 0.00154098
CPL [NCBI] 0.00130508
lymphedema, hereditary, ii [NCBI] 0.00118119
FLT4 [NCBI] 0.000676537
mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly [NCBI] 0.000614201
FOXC2 [NCBI] 0.000551933
yellow nail syndrome [NCBI] 0.000428757
klippel-trenaunay-weber syndrome [NCBI] 0.000415623
lymphedema and ptosis [NCBI] 0.000234146
NS1 [NCBI] 0.00013526
lymphedema, atrial septal defect, and facial changes [NCBI] 0.000116948
lymphedema and cerebral arteriovenous anomaly [NCBI] 0.000116948
hypotrichosis-lymphedema-telangiectasia syndrome [NCBI] 0.000116948
lymphedema, congenital recessive [NCBI] 0.000116948
lymphedema-hypoparathyroidism syndrome [NCBI] 0.000116948
hydrops fetalis, idiopathic [NCBI] 8.60172e-05
LIS2 [NCBI] 8.05207e-05
chorioretinal dysplasia-microcephaly-mental retardation syndrome [NCBI] 7.31844e-05
kanzaki disease [NCBI] 7.04818e-05
PDPN [NCBI] 7.00756e-05
SOX18 [NCBI] 7.00756e-05
IP [NCBI] 6.6499e-05
VEGFC [NCBI] 6.48763e-05
NAGA [NCBI] 5.39062e-05
VEGF [NCBI] 5.09867e-05
RELN [NCBI] 4.88341e-05
SPG7 [NCBI] 4.54987e-05
PEPD [NCBI] 4.39318e-05
CF [NCBI] 3.69138e-05
sotos syndrome [NCBI] 3.62816e-05
aortic valve disease [NCBI] 3.54637e-05
RNASE2 [NCBI] 3.3097e-05
KDR [NCBI] 2.78257e-05
RA [NCBI] 2.05804e-05
HGF [NCBI] 4.29859e-06
AD [NCBI] 3.29349e-06



Database Center for Life Science