Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Prognathism [NCBI]

Gene


 Gene Link Information
Gain		 01
SNX3 [NCBI] 3.73635e-05
NR2E1 [NCBI] 1.59157e-05
TRPS1 [NCBI] 1.34374e-05
MSTN [NCBI] 1.09887e-05
PTPN11 [NCBI] 9.11407e-06
IGF1 [NCBI] 8.61287e-06



OMIM


 OMIM Link Information
gain		 01
prognathism, mandibular [NCBI] 0.00529653
osteodysplasia, familial, anderson type [NCBI] 0.000880362
SHFM2 [NCBI] 0.000647644
GO [NCBI] 0.000605677
PCA [NCBI] 0.000588308
SHFM3 [NCBI] 0.000493306
EEC1 [NCBI] 0.00038891
SHFM1 [NCBI] 0.000376213
AS [NCBI] 0.000272864
MCOPS8 [NCBI] 0.000229097
SNX3 [NCBI] 0.000223417
CCD [NCBI] 0.000202246
brachioskeletogenital syndrome [NCBI] 0.000136591
mental retardation, obesity, mandibular prognathism, and eye and skin anomalies [NCBI] 0.000136591
split-foot deformity with mandibulofacial dysostosis [NCBI] 0.000105643
oroacral syndrome, verloes-koulischer type [NCBI] 0.000100139
SHFM4 [NCBI] 9.27854e-05
ankyloblepharon-ectodermal defects-cleft lip/palate [NCBI] 8.23042e-05
adult syndrome [NCBI] 7.9483e-05
BWS [NCBI] 7.87134e-05
gm1-gangliosidosis, type iii [NCBI] 7.14886e-05
RIEG1 [NCBI] 6.67501e-05
EVC [NCBI] 6.13333e-05
sotos syndrome [NCBI] 5.54634e-05
fragile x mental retardation syndrome [NCBI] 3.82276e-05



Database Center for Life Science