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MeSH keywords -> Related genes, diseases (OMIM)


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01 Maxilla [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.000871862
VCF [NCBI] 0.000336348
FND [NCBI] 0.000312804
ACP5 [NCBI] 6.01851e-05
BMP2 [NCBI] 4.51007e-05
SHH [NCBI] 2.68194e-05
BMP7 [NCBI] 2.1311e-05
IBSP [NCBI] 1.58353e-05
DLX3 [NCBI] 8.2428e-06
BARX1 [NCBI] 7.12398e-06
NGF [NCBI] 6.44123e-06
BMP4 [NCBI] 6.41686e-06
PCNA [NCBI] 6.2218e-06
DLX6 [NCBI] 5.96439e-06
COL9A1 [NCBI] 5.75843e-06
PAX6 [NCBI] 5.58062e-06
MSX1 [NCBI] 5.47655e-06
SH3BP2 [NCBI] 5.40873e-06
PAX9 [NCBI] 5.22922e-06
TGIF1 [NCBI] 5.1253e-06
BST1 [NCBI] 4.96604e-06
CD68 [NCBI] 4.57388e-06
FOXC1 [NCBI] 4.4904e-06
TWIST1 [NCBI] 3.85725e-06
COL2A1 [NCBI] 3.76541e-06
FGF4 [NCBI] 3.76541e-06
PAX3 [NCBI] 3.48883e-06
ACCN4 [NCBI] 3.47476e-06
MEN1 [NCBI] 3.28486e-06
NGFR [NCBI] 3.28486e-06
TTR [NCBI] 2.95899e-06
FGFR3 [NCBI] 2.93198e-06
IL1B [NCBI] 2.73742e-06
PTH [NCBI] 2.72576e-06
ITPR1 [NCBI] 2.69283e-06
NOG [NCBI] 2.47023e-06
GAPDH [NCBI] 2.29993e-06
VDR [NCBI] 1.98913e-06
TJP1 [NCBI] 1.98139e-06
EGF [NCBI] 1.12354e-06
BDNF [NCBI] 1.01136e-06
NPY [NCBI] 6.8108e-07
TNF [NCBI] 1.72531e-07



OMIM


 OMIM Link Information
gain		 01
maxillonasal dysplasia, binder type [NCBI] 0.00641233
apnea, obstructive sleep [NCBI] 0.00329804
STHAG4 [NCBI] 0.00150453
CPI [NCBI] 0.00128126
maxillofacial dysostosis [NCBI] 0.00121566
HFM [NCBI] 0.0011068
SMMCI [NCBI] 0.000875814
palpebral coloboma-lipoma syndrome [NCBI] 0.000789241
PCA [NCBI] 0.00045427
proteus syndrome [NCBI] 0.000333372
cherubism [NCBI] 0.000292902
HPE3 [NCBI] 0.00024806
palatopharyngeal incompetence [NCBI] 0.000247805
teeth, noneruption of, with maxillary hypoplasia and genu valgum [NCBI] 0.000200177
brachioskeletogenital syndrome [NCBI] 0.000200177
radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema [NCBI] 0.000200177
ackerman syndrome [NCBI] 0.000200177
ACP5 [NCBI] 0.000198909
cystic angiomatosis of bone, diffuse [NCBI] 0.000160924
CCD [NCBI] 0.000148582
incisors, shovel-shaped [NCBI] 0.000146123
sakoda complex [NCBI] 0.000146123
arhinia, choanal atresia, and microphthalmia [NCBI] 0.000136519
CDHS [NCBI] 0.000136519
oroacral syndrome, verloes-koulischer type [NCBI] 0.000136519
pseudotrisomy 13 syndrome [NCBI] 0.000105474
OFD1 [NCBI] 8.67497e-05
EVC [NCBI] 8.06848e-05
RIEG1 [NCBI] 7.85931e-05
LSA [NCBI] 7.31446e-05
WS1 [NCBI] 7.00444e-05
RSTS [NCBI] 6.86201e-05
TCOF [NCBI] 6.66178e-05
VWS [NCBI] 6.66178e-05
SRS [NCBI] 6.64376e-05
APS1 [NCBI] 6.47571e-05
DLX6 [NCBI] 5.22273e-05
BCNS [NCBI] 4.81524e-05
DLX5 [NCBI] 4.27472e-05
LHX8 [NCBI] 4.15426e-05
SLOS [NCBI] 3.98211e-05
COL9A1 [NCBI] 3.68355e-05
PITX2 [NCBI] 3.04327e-05
RUNX2 [NCBI] 2.97608e-05
CF [NCBI] 2.78171e-05
PAX3 [NCBI] 2.68262e-05
SPARC [NCBI] 2.46533e-05
PCNA [NCBI] 2.24124e-05
NGFR [NCBI] 1.86371e-05
NGFB [NCBI] 1.79078e-05
TTR [NCBI] 1.28228e-05
GAPDH [NCBI] 9.09864e-06
TNFRSF11B [NCBI] 8.63471e-06
GNRH1 [NCBI] 7.90271e-06
SPP1 [NCBI] 7.41989e-06
SHH [NCBI] 7.13687e-06
PTH [NCBI] 6.19584e-06
BDNF [NCBI] 1.37696e-06
TNF [NCBI] 8.51175e-07
NPY [NCBI] 2.2266e-07
EGF [NCBI] 6.95817e-08



Database Center for Life Science