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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cervical Vertebrae [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.00101447
FOP [NCBI] 0.000568566
HFM [NCBI] 0.000327612
AIS [NCBI] 0.000201565
BMP2 [NCBI] 8.88687e-05
BMP7 [NCBI] 1.11417e-05
PAX1 [NCBI] 9.61972e-06
CD99 [NCBI] 8.16581e-06
NOG [NCBI] 6.26073e-06
AGPAT2 [NCBI] 6.19894e-06
ARSE [NCBI] 5.9981e-06
TBX5 [NCBI] 5.78091e-06
LHX3 [NCBI] 5.68779e-06
ATXN7 [NCBI] 5.68779e-06
LOXL1 [NCBI] 5.60262e-06
TRAPPC2 [NCBI] 5.48711e-06
BSCL2 [NCBI] 5.48711e-06
HOXB5 [NCBI] 5.45139e-06
PPARGC1B [NCBI] 5.38358e-06
TBX3 [NCBI] 5.35133e-06
SOD1 [NCBI] 5.2202e-06
AMPD1 [NCBI] 5.17707e-06
HOXA5 [NCBI] 5.0758e-06
GHSR [NCBI] 4.94091e-06
ABCC6 [NCBI] 4.76766e-06
PDE4B [NCBI] 4.69939e-06
ACVR1 [NCBI] 4.62015e-06
CD68 [NCBI] 4.52518e-06
NCAN [NCBI] 4.27603e-06
COL3A1 [NCBI] 4.18356e-06
ZBTB16 [NCBI] 4.10804e-06
PIP [NCBI] 4.09899e-06
ATP7A [NCBI] 3.88884e-06
SMARCB1 [NCBI] 3.8186e-06
PPARGC1A [NCBI] 3.59517e-06
ITGAM [NCBI] 3.55289e-06
RUNX2 [NCBI] 3.42685e-06
MGP [NCBI] 3.39113e-06
KRT7 [NCBI] 3.31118e-06
VCAN [NCBI] 3.31118e-06
NGFR [NCBI] 3.26003e-06
BDNF [NCBI] 3.21937e-06
LEP [NCBI] 3.09154e-06
SOX9 [NCBI] 3.08512e-06
ADCYAP1 [NCBI] 3.04438e-06
GFAP [NCBI] 2.90044e-06
TP63 [NCBI] 2.79207e-06
IGF1 [NCBI] 2.76416e-06
NOS1 [NCBI] 2.71502e-06
NEFH [NCBI] 2.63971e-06
BCR [NCBI] 2.62772e-06
OPRL1 [NCBI] 2.59455e-06
IL10 [NCBI] 2.57745e-06
NPY [NCBI] 2.48091e-06
CAV1 [NCBI] 2.34067e-06
MOG [NCBI] 2.32185e-06
IL8 [NCBI] 2.31045e-06
PTHLH [NCBI] 2.2595e-06
CNTF [NCBI] 2.21758e-06
VDR [NCBI] 1.96529e-06
PTEN [NCBI] 1.88202e-06
APOE [NCBI] 1.59927e-06
CAT [NCBI] 1.4443e-06
NOS2 [NCBI] 1.36468e-06
MBP [NCBI] 1.22912e-06
CHAT [NCBI] 1.22912e-06
PCNA [NCBI] 1.03862e-06
VIP [NCBI] 9.20556e-07
PTH [NCBI] 7.48695e-07
TH [NCBI] 7.4545e-07
CASP3 [NCBI] 5.03173e-07
NGF [NCBI] 4.31623e-07
TNF [NCBI] 1.6065e-07




OMIM


OMIM Link Information
gain
01
RA [NCBI] 0.00136898
vertebral hypoplasia with lumbar kyphosis [NCBI] 0.00131262
chiari malformation type i [NCBI] 0.00123859
leri pleonosteosis [NCBI] 0.00100225
palatopharyngeal incompetence [NCBI] 0.000977208
mesomelic dysplasia, kantaputra type [NCBI] 0.000885498
TKCR [NCBI] 0.000809899
HFM [NCBI] 0.000741897
klippel-feil syndrome, autosomal dominant [NCBI] 0.000709304
fibrochondrogenesis [NCBI] 0.000709304
murcs association [NCBI] 0.000703316
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000613355
amyotrophy, monomelic [NCBI] 0.000589007
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000589007
DURS1 [NCBI] 0.000567166
IS1 [NCBI] 0.000429677
SCDO1 [NCBI] 0.00022579
FOP [NCBI] 0.000223281
microcephaly with cervical spine fusion anomalies [NCBI] 0.000170157
spondylocamptodactyly [NCBI] 0.000170157
mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones [NCBI] 0.000170157
ACH [NCBI] 0.000167244
CF [NCBI] 0.000164608
cervical rib [NCBI] 0.000130949
NSX [NCBI] 0.000130949
spondylosis, cervical [NCBI] 0.000130949
otofaciocervical syndrome [NCBI] 0.000130949
SLE [NCBI] 0.000124301
CRMO [NCBI] 0.000118188
ankylosing vertebral hyperostosis with tylosis [NCBI] 0.000116194
camptomelic syndrome, long-limb type [NCBI] 0.000106636
IDD [NCBI] 9.9547e-05
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 9.39118e-05
spondylocarpotarsal synostosis syndrome [NCBI] 8.92372e-05
OPLL [NCBI] 8.17643e-05
wildervanck syndrome [NCBI] 8.17643e-05
rokitansky-kuster-hauser syndrome [NCBI] 7.86793e-05
SEDT [NCBI] 7.86793e-05
mucopolysaccharidosis type iva [NCBI] 7.70851e-05
DMC [NCBI] 7.34014e-05
pituitary dwarfism iii [NCBI] 7.11073e-05
weaver syndrome [NCBI] 6.89953e-05
DRRS [NCBI] 6.89953e-05
EDMD2 [NCBI] 6.70395e-05
apert syndrome [NCBI] 6.70395e-05
CDPX1 [NCBI] 6.52189e-05
HOXA3 [NCBI] 6.37916e-05
CMDD [NCBI] 6.35166e-05
SEDC [NCBI] 5.89913e-05
mucopolysaccharidosis type vi [NCBI] 5.63638e-05
SLC35A3 [NCBI] 5.38089e-05
LQT1 [NCBI] 5.07871e-05
RSMD1 [NCBI] 5.07871e-05
CDX1 [NCBI] 4.75955e-05
LWD [NCBI] 4.70824e-05
RCDP1 [NCBI] 4.62379e-05
SCS [NCBI] 4.31294e-05
HOXD3 [NCBI] 4.20915e-05
ARSE [NCBI] 4.119e-05
campomelic dysplasia [NCBI] 4.10398e-05
LHX3 [NCBI] 3.7347e-05
MOG [NCBI] 3.7347e-05
SLC1A3 [NCBI] 3.68675e-05
CD [NCBI] 3.51944e-05
GHSR [NCBI] 3.48585e-05
CCD [NCBI] 2.78658e-05
BCNS [NCBI] 2.19744e-05
CPI [NCBI] 1.97346e-05
SMAX1 [NCBI] 1.67582e-05
SLOS [NCBI] 1.51084e-05
BDNF [NCBI] 1.17819e-05
PXE [NCBI] 1.14768e-05
ACP5 [NCBI] 1.11863e-05
CNTF [NCBI] 9.74351e-06
GFAP [NCBI] 9.66584e-06
PPARA [NCBI] 9.21991e-06
SPP1 [NCBI] 8.78455e-06
GDNF [NCBI] 8.05605e-06
NPY [NCBI] 7.12091e-06
FMF [NCBI] 6.11129e-06
KLK3 [NCBI] 5.32711e-06
CVID [NCBI] 5.31379e-06
CAT [NCBI] 4.8782e-06
apnea, obstructive sleep [NCBI] 4.32766e-06
MBP [NCBI] 3.56277e-06
CHAT [NCBI] 3.47382e-06
lymphoma, non-hodgkin, familial [NCBI] 3.38332e-06
PCNA [NCBI] 2.54724e-06
VIP [NCBI] 1.8317e-06
PTH [NCBI] 1.09788e-06
TH [NCBI] 1.03626e-06
ALD [NCBI] 8.79788e-07
NGFB [NCBI] 8.32456e-08
VEGF [NCBI] 7.48148e-08




Database Center for Life Science