MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Arachnoid
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
8.69867e-05
FOXC1
[NCBI]
1.31141e-05
DSP
[NCBI]
1.14336e-05
CST3
[NCBI]
9.69496e-06
GJB2
[NCBI]
9.44923e-06
CTF1
[NCBI]
7.72876e-06
CD68
[NCBI]
7.24224e-06
YY1AP1
[NCBI]
6.89281e-06
PKP2
[NCBI]
6.81997e-06
PTGDS
[NCBI]
6.6885e-06
DSC3
[NCBI]
6.65817e-06
YAP1
[NCBI]
6.39673e-06
DSC2
[NCBI]
6.3087e-06
CADM1
[NCBI]
6.08331e-06
DSG2
[NCBI]
6.05023e-06
NF2
[NCBI]
5.80608e-06
CCNE1
[NCBI]
5.36927e-06
MSLN
[NCBI]
5.26027e-06
GJA1
[NCBI]
4.99049e-06
SELPLG
[NCBI]
4.075e-06
CCR7
[NCBI]
4.04197e-06
COMT
[NCBI]
3.91419e-06
BMP2
[NCBI]
2.98582e-06
APOE
[NCBI]
2.90877e-06
VWF
[NCBI]
2.65696e-06
TH
[NCBI]
1.95318e-06
PRL
[NCBI]
1.86228e-06
OMIM
OMIM
Link
Information
gain
01
hemophagocytic lymphohistiocytosis, familial, 1
[NCBI]
0.00199615
spinal arachnoiditis
[NCBI]
0.0017631
arachnoid cysts, intracranial
[NCBI]
0.000390315
melanosis, neurocutaneous
[NCBI]
0.000365873
amyloidosis vi
[NCBI]
0.000326873
MFS
[NCBI]
0.000263793
lymphedema-distichiasis syndrome
[NCBI]
0.000254733
spinal intradural arachnoid cysts
[NCBI]
0.000221495
intracranial hypertension, idiopathic
[NCBI]
0.000182229
amyloidosis vii
[NCBI]
0.000126664
hurler syndrome
[NCBI]
9.01537e-05
fabry disease
[NCBI]
7.0066e-05
DSC3
[NCBI]
4.71224e-05
DSC2
[NCBI]
4.49449e-05
DSG2
[NCBI]
4.3276e-05
temporal arteritis
[NCBI]
4.29725e-05
tay-sachs disease, ab variant
[NCBI]
4.19225e-05
FOXC1
[NCBI]
4.15226e-05
AT
[NCBI]
4.13695e-05
AD
[NCBI]
3.05912e-05
GJB2
[NCBI]
2.92982e-05
CEACAM5
[NCBI]
2.7819e-05
GJA1
[NCBI]
2.0521e-05
TTR
[NCBI]
2.00329e-05
COMT
[NCBI]
1.89376e-05
MUC1
[NCBI]
1.88419e-05
APOE
[NCBI]
1.19881e-05
KLK3
[NCBI]
1.03812e-05
SLE
[NCBI]
6.96067e-06
TH
[NCBI]
4.72994e-06
PRL
[NCBI]
4.2328e-06
VEGF
[NCBI]
1.3573e-06
Database Center for Life Science