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MeSH keywords -> Related genes, diseases (OMIM)


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01 Noonan Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
PTPN11 [NCBI] 0.00146882
NS2 [NCBI] 0.000499621
KRAS [NCBI] 9.34041e-05
SOS1 [NCBI] 6.6824e-05
PTPN7 [NCBI] 3.56028e-05
BRAF [NCBI] 3.019e-05
MAP2K2 [NCBI] 2.94712e-05
RAF1 [NCBI] 2.38319e-05
RPS4X [NCBI] 2.20578e-05
NF1 [NCBI] 1.97264e-05
HRAS [NCBI] 1.96274e-05
SH3BP2 [NCBI] 1.72919e-05
GAB1 [NCBI] 1.5667e-05
DTX1 [NCBI] 1.48846e-05
FOXC2 [NCBI] 1.42557e-05
SOS2 [NCBI] 1.16061e-05
PTPN6 [NCBI] 1.11585e-05
ARAF [NCBI] 1.10229e-05
MRAS [NCBI] 9.95664e-06
RPL6 [NCBI] 9.95664e-06
EPS8 [NCBI] 9.71078e-06
PAG1 [NCBI] 9.71078e-06
RPS4Y1 [NCBI] 9.71078e-06
MAP2K1 [NCBI] 9.31636e-06
PTPN12 [NCBI] 8.70234e-06
SLC16A2 [NCBI] 7.30747e-06
TGIF1 [NCBI] 7.00083e-06
DCN [NCBI] 6.74125e-06
PTPN1 [NCBI] 6.66287e-06
PDGFRB [NCBI] 6.38132e-06
CSK [NCBI] 6.28678e-06
GH1 [NCBI] 5.63465e-06
STAT5B [NCBI] 5.23077e-06
STAT5A [NCBI] 5.18259e-06
SHOX [NCBI] 4.91973e-06
APAF1 [NCBI] 4.17426e-06
FLT3 [NCBI] 2.52109e-06
AR [NCBI] 6.04552e-07
PRL [NCBI] 4.15845e-07
CASP3 [NCBI] 2.72535e-07
PTH [NCBI] 1.08147e-07



OMIM


 OMIM Link Information
gain		 01
NS1 [NCBI] 0.00653145
noonan syndrome 2 [NCBI] 0.00337444
NFNS [NCBI] 0.00172536
cardiofaciocutaneous syndrome [NCBI] 0.00170245
PTPN11 [NCBI] 0.00147524
gonadal dysgenesis, xy type [NCBI] 0.000672238
leopard syndrome 1 [NCBI] 0.00066378
noonan-like/multiple giant cell lesion syndrome [NCBI] 0.000633623
OD [NCBI] 0.000553188
costello syndrome [NCBI] 0.0004138
NS4 [NCBI] 0.000320797
NF1 [NCBI] 0.000319504
JMML [NCBI] 0.000285091
watson syndrome [NCBI] 0.000253445
NS5 [NCBI] 0.000213732
noonan-like syndrome with loose anagen hair [NCBI] 0.000213732
SOS1 [NCBI] 0.000207155
SLE [NCBI] 0.000193728
KRAS [NCBI] 0.000121867
RPS4X [NCBI] 0.000118566
RAF1 [NCBI] 0.000110462
leopard syndrome 2 [NCBI] 0.000106799
noonan syndrome 3 [NCBI] 8.4349e-05
coxoauricular syndrome [NCBI] 8.4349e-05
EPS8 [NCBI] 7.99824e-05
HRAS [NCBI] 7.76772e-05
IGFALS [NCBI] 6.74505e-05
DTX1 [NCBI] 6.62048e-05
loose anagen hair syndrome [NCBI] 6.30874e-05
HPE4 [NCBI] 6.30874e-05
RPS4Y [NCBI] 6.10065e-05
RCM1 [NCBI] 5.80937e-05
opitz syndrome [NCBI] 5.43016e-05
TMAU [NCBI] 4.99164e-05
lymphedema, hereditary, i [NCBI] 4.99164e-05
APAF1 [NCBI] 4.76952e-05
DCN [NCBI] 4.1095e-05
faciogenital dysplasia [NCBI] 3.58534e-05
GDXY [NCBI] 3.52388e-05
spermatogenic failure, nonobstructive, y-linked [NCBI] 3.14786e-05
LWD [NCBI] 2.93725e-05
MHS1 [NCBI] 2.54174e-05
CMH [NCBI] 1.25628e-05
WBS [NCBI] 9.22988e-06
thrombocytopenic purpura, autoimmune [NCBI] 2.64198e-06
PTH [NCBI] 2.69323e-07
PRL [NCBI] 8.36834e-08



Database Center for Life Science