MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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