MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Spinal Cord Neoplasms
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
0.000348762
GFAP
[NCBI]
9.81406e-05
VUR
[NCBI]
5.24233e-05
VHL
[NCBI]
4.05307e-05
CD99
[NCBI]
2.0938e-05
EPB41L3
[NCBI]
2.04188e-05
SMARCB1
[NCBI]
1.52137e-05
NF1
[NCBI]
1.50912e-05
MEN1
[NCBI]
1.15964e-05
EPB41
[NCBI]
9.83367e-06
CXCR6
[NCBI]
8.1818e-06
EGFR
[NCBI]
7.95345e-06
CXCL16
[NCBI]
7.95106e-06
TNC
[NCBI]
7.80348e-06
KRIT1
[NCBI]
7.2324e-06
PTEN
[NCBI]
7.20619e-06
SDHD
[NCBI]
7.15342e-06
EPB41L2
[NCBI]
6.34142e-06
PIP
[NCBI]
6.28275e-06
BSG
[NCBI]
6.04645e-06
PAX3
[NCBI]
5.49623e-06
PCNA
[NCBI]
5.25628e-06
ABCG2
[NCBI]
4.77169e-06
ALK
[NCBI]
4.6724e-06
CDKN2B
[NCBI]
4.41007e-06
CDH1
[NCBI]
4.41007e-06
APC
[NCBI]
3.13356e-06
TG
[NCBI]
2.97968e-06
HRAS
[NCBI]
2.87041e-06
MBP
[NCBI]
2.33573e-06
PRL
[NCBI]
1.60343e-06
EGF
[NCBI]
9.41162e-07
TNF
[NCBI]
2.64082e-07
OMIM
OMIM
Link
Information
gain
01
angioma, hereditary neurocutaneous
[NCBI]
0.00206499
chiari malformation type i
[NCBI]
0.000626005
VHL
[NCBI]
0.000494826
GFAP
[NCBI]
0.000377093
meningioma, familial
[NCBI]
0.00021939
CCM
[NCBI]
0.0002056
RDT
[NCBI]
0.000187889
lipomyelomeningocele
[NCBI]
0.000131618
MUC1
[NCBI]
0.000116601
neurofibromatosis, familial spinal
[NCBI]
9.1078e-05
schwannomatosis
[NCBI]
7.58729e-05
lymphedema-distichiasis syndrome
[NCBI]
6.57736e-05
PGL1
[NCBI]
5.4453e-05
NF2
[NCBI]
4.84154e-05
NF1
[NCBI]
4.42191e-05
SDHD
[NCBI]
4.08564e-05
CD
[NCBI]
3.88292e-05
fragile x mental retardation syndrome
[NCBI]
3.34639e-05
RA
[NCBI]
3.28911e-05
DFSP
[NCBI]
2.80488e-05
AT
[NCBI]
2.29866e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
[NCBI]
1.99936e-05
lymphoma, non-hodgkin, familial
[NCBI]
1.1014e-05
PCNA
[NCBI]
8.36155e-06
VEGF
[NCBI]
8.15099e-06
TG
[NCBI]
5.72124e-06
EGFR
[NCBI]
5.34975e-06
CEACAM5
[NCBI]
3.37621e-06
MBP
[NCBI]
2.98866e-06
TNF
[NCBI]
2.153e-06
PRL
[NCBI]
5.3714e-07
EGF
[NCBI]
6.66967e-08
KLK3
[NCBI]
2.52616e-08
Database Center for Life Science