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MeSH keywords -> Related genes, diseases (OMIM)


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01 Spinal Cord Compression [NCBI]


Gene


Gene Link Information
Gain
01
AIS [NCBI] 0.000125549
MS [NCBI] 7.55426e-05
NEFH [NCBI] 1.43899e-05
CD99 [NCBI] 1.40174e-05
GFAP [NCBI] 1.30626e-05
BMP2 [NCBI] 1.19041e-05
PAX1 [NCBI] 1.01586e-05
BDNF [NCBI] 9.32461e-06
CD68 [NCBI] 8.78927e-06
PLD1 [NCBI] 8.65446e-06
S100B [NCBI] 8.53728e-06
IDS [NCBI] 7.94514e-06
EPO [NCBI] 7.15986e-06
MPO [NCBI] 7.10346e-06
MAP2 [NCBI] 6.66883e-06
BMP7 [NCBI] 5.91294e-06
CHAT [NCBI] 4.5374e-06
TRH [NCBI] 3.74785e-06
SOD1 [NCBI] 3.60384e-06
LPL [NCBI] 3.3605e-06
PTEN [NCBI] 3.15812e-06
MBP [NCBI] 3.00912e-06
NGF [NCBI] 2.44621e-06
TP53 [NCBI] 2.3394e-06
APOE [NCBI] 2.14031e-06
CASP3 [NCBI] 1.98751e-06
PTH [NCBI] 1.63047e-06
EGF [NCBI] 1.50854e-06
TNF [NCBI] 6.75253e-07




OMIM


OMIM Link Information
gain
01
angioma, hereditary neurocutaneous [NCBI] 0.000742146
syringomyelia, isolated [NCBI] 0.000715905
CGF [NCBI] 0.000561
chiari malformation type i [NCBI] 0.000502484
ACH [NCBI] 0.000411326
proteus syndrome [NCBI] 0.000409827
mucopolysaccharidosis type vi [NCBI] 0.000280974
DMC [NCBI] 0.000231506
IS1 [NCBI] 0.000191368
multiple exostoses with spastic tetraparesis [NCBI] 0.000119634
microcephaly with cervical spine fusion anomalies [NCBI] 0.000119634
SEDC [NCBI] 0.000113781
exostoses, multiple, type i [NCBI] 0.000111214
mucopolysaccharidosis type iva [NCBI] 8.5492e-05
lymphoma, non-hodgkin, familial [NCBI] 8.03877e-05
melanosis, neurocutaneous [NCBI] 7.91149e-05
SMC [NCBI] 7.58609e-05
RA [NCBI] 7.4851e-05
SLE [NCBI] 6.72755e-05
OPLL [NCBI] 6.54125e-05
SYNS1 [NCBI] 6.26044e-05
sitosterolemia [NCBI] 5.91458e-05
CDPX1 [NCBI] 5.63069e-05
osteogenesis imperfecta, type iv [NCBI] 5.54634e-05
ARSE [NCBI] 5.48997e-05
CMDD [NCBI] 5.46625e-05
lymphedema-distichiasis syndrome [NCBI] 5.39003e-05
osteogenesis imperfecta, type iii [NCBI] 5.31732e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 4.03473e-05
CRMO [NCBI] 3.6521e-05
CMT1A [NCBI] 3.55857e-05
GFAP [NCBI] 3.33442e-05
RDT [NCBI] 3.27115e-05
osteogenesis imperfecta, type i [NCBI] 3.23432e-05
mucopolysaccharidosis type ii [NCBI] 2.88919e-05
MAP2 [NCBI] 2.71118e-05
BDNF [NCBI] 2.61268e-05
KLK3 [NCBI] 1.79298e-05
EPO [NCBI] 1.46242e-05
MPO [NCBI] 1.46172e-05
CHAT [NCBI] 1.20228e-05
TNFSF6 [NCBI] 8.9325e-06
temporal arteritis [NCBI] 8.53675e-06
LPL [NCBI] 6.76066e-06
VEGF [NCBI] 5.8349e-06
MBP [NCBI] 4.7374e-06
NGFB [NCBI] 2.41265e-06
TNF [NCBI] 5.63063e-07
PTH [NCBI] 3.21473e-07
CEACAM5 [NCBI] 2.10318e-07
EGF [NCBI] 1.21977e-07




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