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01 Median Nerve [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00205306
AIS [NCBI] 6.66298e-05
PMP22 [NCBI] 4.07764e-05
MPZ [NCBI] 3.48468e-05
SLC12A6 [NCBI] 1.42776e-05
GJB1 [NCBI] 1.3015e-05
MAG [NCBI] 1.23645e-05
MPZL1 [NCBI] 7.39899e-06
SOD1 [NCBI] 6.90194e-06
CHRNA1 [NCBI] 6.3347e-06
GDAP1 [NCBI] 6.26444e-06
CLCN1 [NCBI] 4.98075e-06
TOR1A [NCBI] 4.92601e-06
UBE3A [NCBI] 4.7702e-06
CACNA1A [NCBI] 4.71843e-06
ALDH2 [NCBI] 4.61582e-06
ACHE [NCBI] 4.43204e-06
MECP2 [NCBI] 4.04393e-06
ERBB4 [NCBI] 3.52515e-06
NGF [NCBI] 3.45064e-06
OPRL1 [NCBI] 3.42679e-06
CNTF [NCBI] 3.04209e-06
CTGF [NCBI] 2.94717e-06
TRH [NCBI] 2.12263e-06
NPY [NCBI] 1.37194e-06



OMIM


 OMIM Link Information
gain		 01
hereditary motor and sensory neuropathy v [NCBI] 0.00220681
neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [NCBI] 0.00120455
auditory neuropathy, autosomal dominant, 1 [NCBI] 0.00108741
SCAX1 [NCBI] 0.000910064
CTS1 [NCBI] 0.000766001
SPS [NCBI] 0.0005979
median-ulnar nerve communications [NCBI] 0.000384054
ALD [NCBI] 0.000327206
IS1 [NCBI] 0.00024889
ACCPN [NCBI] 0.000221759
SPG3A [NCBI] 0.000206662
posterior column ataxia [NCBI] 0.000191783
KSS [NCBI] 0.000190938
MPZ [NCBI] 0.000163684
CMT1B [NCBI] 0.000160282
slowed nerve conduction velocity, autosomal dominant [NCBI] 0.000152538
spinocerebellar ataxia, x-linked 3 [NCBI] 0.000152538
megalodactyly [NCBI] 0.000152538
HNPP [NCBI] 0.000151148
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy [NCBI] 0.000137745
charcot-marie-tooth disease, dominant intermediate b [NCBI] 0.000121024
charcot-marie-tooth disease, axonal, type 2j [NCBI] 0.000115351
encephalopathy, neonatal severe, due to mecp2 mutations [NCBI] 0.000115351
PLSJ [NCBI] 0.000110639
SCAR1 [NCBI] 0.000103091
hyperekplexia, hereditary [NCBI] 0.000103091
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 9.71634e-05
SCCMS [NCBI] 9.46165e-05
PMP22 [NCBI] 9.37888e-05
EAOH [NCBI] 8.81425e-05
MJD [NCBI] 8.64465e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 7.47493e-05
cerebrotendinous xanthomatosis [NCBI] 6.94447e-05
CMTX1 [NCBI] 6.75875e-05
CJD [NCBI] 6.29039e-05
hypertrophic neuropathy of dejerine-sottas [NCBI] 6.05518e-05
SLC12A6 [NCBI] 5.35538e-05
CCT4 [NCBI] 5.11072e-05
CMT1A [NCBI] 4.95906e-05
SLC17A8 [NCBI] 4.31777e-05
PMD [NCBI] 3.68266e-05
PD [NCBI] 3.38712e-05
DRPLA [NCBI] 3.23971e-05
RTT [NCBI] 3.058e-05
MECP2 [NCBI] 2.8202e-05
GJB1 [NCBI] 2.64823e-05
RA [NCBI] 2.3629e-05
SOD1 [NCBI] 2.17395e-05
FMF [NCBI] 2.05154e-05
lymphoma, non-hodgkin, familial [NCBI] 1.61372e-05
ACHE [NCBI] 1.50656e-05
CNTF [NCBI] 1.29628e-05
NGFB [NCBI] 8.95255e-06
PWS [NCBI] 5.69303e-06
SLE [NCBI] 4.32018e-06
thrombocytopenic purpura, autoimmune [NCBI] 3.00591e-06
NPY [NCBI] 2.50024e-06



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