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01 Thoracic Vertebrae [NCBI]


Gene


Gene Link Information
Gain
01
AIS [NCBI] 0.0134697
MS [NCBI] 6.50977e-05
BMP7 [NCBI] 1.69931e-05
BMP2 [NCBI] 1.30492e-05
GFAP [NCBI] 1.28292e-05
KRIT1 [NCBI] 1.1822e-05
PAX1 [NCBI] 1.00969e-05
BDNF [NCBI] 1.0042e-05
CD99 [NCBI] 8.6416e-06
MESP2 [NCBI] 7.79081e-06
NOS1 [NCBI] 7.28083e-06
NEFH [NCBI] 7.12759e-06
OSCAR [NCBI] 6.59688e-06
DLL3 [NCBI] 6.12094e-06
TBX5 [NCBI] 6.01821e-06
PTH [NCBI] 5.82619e-06
TRAPPC2 [NCBI] 5.72432e-06
HOXB5 [NCBI] 5.6886e-06
TBX3 [NCBI] 5.5885e-06
ADAMTS4 [NCBI] 5.46896e-06
PAX9 [NCBI] 5.44119e-06
CLEC3B [NCBI] 5.36222e-06
HOXA5 [NCBI] 5.31285e-06
HOXB7 [NCBI] 5.22088e-06
ADAMTS5 [NCBI] 4.93622e-06
PDLIM7 [NCBI] 4.72839e-06
NCAN [NCBI] 4.51248e-06
MBP [NCBI] 4.18937e-06
ADAMTS2 [NCBI] 4.08897e-06
BMI1 [NCBI] 4.08897e-06
COL2A1 [NCBI] 3.97611e-06
ACCN4 [NCBI] 3.68489e-06
PLD1 [NCBI] 3.57045e-06
TP63 [NCBI] 3.02472e-06
VHL [NCBI] 2.93206e-06
NPY [NCBI] 2.90822e-06
OPRL1 [NCBI] 2.8261e-06
IL10 [NCBI] 2.80889e-06
NOG [NCBI] 2.67641e-06
PTHLH [NCBI] 2.48856e-06
TG [NCBI] 2.44498e-06
NGF [NCBI] 2.33562e-06
ACP5 [NCBI] 2.22427e-06
PTEN [NCBI] 2.10696e-06
CD68 [NCBI] 1.82299e-06
TRH [NCBI] 1.55064e-06
CHAT [NCBI] 1.44091e-06
VEGFA [NCBI] 1.37501e-06
PCNA [NCBI] 1.24407e-06
VIP [NCBI] 1.12115e-06
TH [NCBI] 9.37081e-07
TNF [NCBI] 2.85044e-07




OMIM


OMIM Link Information
gain
01
IS1 [NCBI] 0.0403319
costovertebral segmentation anomalies [NCBI] 0.00270787
cerebrofaciothoracic dysplasia [NCBI] 0.00170983
SCDO1 [NCBI] 0.00169204
vertebral hypoplasia with lumbar kyphosis [NCBI] 0.00106614
TKCR [NCBI] 0.000567314
CRMO [NCBI] 0.000530664
ankylosing vertebral hyperostosis with tylosis [NCBI] 0.000327127
murcs association [NCBI] 0.000253937
robinow syndrome, autosomal dominant [NCBI] 0.000243818
spinal intradural arachnoid cysts [NCBI] 0.000190366
dwarfism with tall vertebrae [NCBI] 0.000190366
spondylospinal thoracic dysostosis [NCBI] 0.000190366
NSX [NCBI] 0.000151123
ALGS1 [NCBI] 0.00014718
rhizomelic dysplasia, patterson-lowry type [NCBI] 0.000136332
OPTA1 [NCBI] 0.000136332
vacterl association with hydrocephalus [NCBI] 0.000126738
native american myopathy [NCBI] 0.000126738
spondylocarpotarsal synostosis syndrome [NCBI] 0.000109232
OPTA2 [NCBI] 0.000109232
three m syndrome [NCBI] 0.000105205
OPLL [NCBI] 0.000101688
wildervanck syndrome [NCBI] 0.000101688
rokitansky-kuster-hauser syndrome [NCBI] 9.85672e-05
SEDT [NCBI] 9.85672e-05
DRRS [NCBI] 8.87405e-05
DLL3 [NCBI] 8.16453e-05
robinow syndrome, autosomal recessive [NCBI] 7.71391e-05
exostoses, multiple, type i [NCBI] 7.71391e-05
mucopolysaccharidosis type vii [NCBI] 7.45691e-05
LQT1 [NCBI] 7.00683e-05
RSMD1 [NCBI] 7.00683e-05
lymphoma, non-hodgkin, familial [NCBI] 6.18616e-05
CCM [NCBI] 5.92e-05
RDT [NCBI] 5.59929e-05
CLS [NCBI] 5.31458e-05
SVAS [NCBI] 5.31458e-05
SLC35A3 [NCBI] 5.24331e-05
GFAP [NCBI] 4.72272e-05
CDX1 [NCBI] 4.62201e-05
ACH [NCBI] 4.49701e-05
SLE [NCBI] 4.32362e-05
BCNS [NCBI] 3.91841e-05
BMI1 [NCBI] 3.76405e-05
BDNF [NCBI] 3.64767e-05
PMD [NCBI] 3.55719e-05
SMAX1 [NCBI] 3.31458e-05
NF1 [NCBI] 1.80547e-05
SLC18A3 [NCBI] 1.74238e-05
temporal arteritis [NCBI] 1.68315e-05
PTH [NCBI] 1.63931e-05
MBP [NCBI] 1.28046e-05
VEGF [NCBI] 1.24661e-05
MUC1 [NCBI] 1.18788e-05
ADCYAP1 [NCBI] 9.03374e-06
TG [NCBI] 8.64773e-06
RA [NCBI] 5.40193e-06
NPY [NCBI] 5.26227e-06
KLK3 [NCBI] 4.28219e-06
CEACAM5 [NCBI] 3.23488e-06
NGFB [NCBI] 2.63753e-06
CHAT [NCBI] 2.56695e-06
PCNA [NCBI] 1.74168e-06
VIP [NCBI] 1.13076e-06
AVP [NCBI] 1.103e-06
TNF [NCBI] 7.38842e-07
TH [NCBI] 5.01516e-07




Database Center for Life Science