MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Reflex, Stretch
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
0.000242384
FXN
[NCBI]
9.1502e-06
ACCN4
[NCBI]
6.1403e-06
CNTNAP2
[NCBI]
3.63238e-06
HAS3
[NCBI]
3.5355e-06
MAG
[NCBI]
3.236e-06
HAS2
[NCBI]
3.18711e-06
GLRA1
[NCBI]
3.18135e-06
L1CAM
[NCBI]
3.0932e-06
RAB7A
[NCBI]
2.68557e-06
PMP22
[NCBI]
2.40191e-06
TRH
[NCBI]
1.74931e-06
AFP
[NCBI]
1.74186e-06
OMIM
OMIM
Link
Information
gain
01
EOCA
[NCBI]
0.00805154
DA10
[NCBI]
0.00127744
CMT2B2
[NCBI]
0.000847798
hereditary motor and sensory neuropathy v
[NCBI]
0.000761393
amyotrophy, monomelic
[NCBI]
0.000729587
FRDA
[NCBI]
0.000502569
dystonia with ringbinden
[NCBI]
0.000158423
cortical dysplasia-focal epilepsy syndrome
[NCBI]
0.000158423
amenorrhea-galactorrhea syndrome
[NCBI]
0.000130657
GRTH
[NCBI]
0.000104299
thyrotropin deficiency, isolated
[NCBI]
0.000104299
INAD1
[NCBI]
9.55827e-05
LGMD1A
[NCBI]
9.13596e-05
HMN5
[NCBI]
8.63434e-05
cerebrotendinous xanthomatosis
[NCBI]
8.63434e-05
HNA
[NCBI]
8.00649e-05
niemann-pick disease, type a
[NCBI]
7.61714e-05
TGD
[NCBI]
7.61714e-05
RMD
[NCBI]
7.53072e-05
HYPP
[NCBI]
6.60447e-05
RSTS
[NCBI]
6.45244e-05
AMC
[NCBI]
6.0569e-05
ALS1
[NCBI]
5.44854e-05
SCA2
[NCBI]
5.33609e-05
CNTNAP2
[NCBI]
5.02492e-05
SCA1
[NCBI]
4.79397e-05
L1CAM
[NCBI]
3.45946e-05
FXN
[NCBI]
3.39014e-05
THRB
[NCBI]
3.20441e-05
FRAP1
[NCBI]
1.85667e-05
RA
[NCBI]
1.35368e-05
AFP
[NCBI]
1.20134e-05
MG
[NCBI]
6.61328e-06
Database Center for Life Science