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