Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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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