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01 Peripheral Nervous System Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00081151
PMP22 [NCBI] 0.000381627
CMT2H [NCBI] 0.000298173
SCAR3 [NCBI] 0.000298173
EKV3 [NCBI] 0.000298173
CMT2G [NCBI] 0.000298173
SCA25 [NCBI] 0.000237475
AUNX1 [NCBI] 0.000237475
TTR [NCBI] 0.000216632
NGF [NCBI] 0.000211542
MAG [NCBI] 0.000114675
HFM [NCBI] 9.20706e-05
WG [NCBI] 8.40857e-05
MPZ [NCBI] 5.5727e-05
GJB1 [NCBI] 4.51049e-05
BDNF [NCBI] 3.86564e-05
LIF [NCBI] 3.72964e-05
SACS [NCBI] 3.3288e-05
GFAP [NCBI] 3.21968e-05
GAN [NCBI] 2.66527e-05
NEFH [NCBI] 2.33642e-05
TRPV1 [NCBI] 2.23599e-05
CNTF [NCBI] 2.14732e-05
GJB3 [NCBI] 1.87869e-05
TYMP [NCBI] 1.87059e-05
ACHE [NCBI] 1.86752e-05
CD68 [NCBI] 1.76696e-05
SH3TC2 [NCBI] 1.70741e-05
POLG [NCBI] 1.62208e-05
MBP [NCBI] 1.61725e-05
GDNF [NCBI] 1.58603e-05
SETX [NCBI] 1.48579e-05
TMEM167A [NCBI] 1.3173e-05
ATL1 [NCBI] 1.28338e-05
NPY [NCBI] 1.27102e-05
KCNA1 [NCBI] 1.26592e-05
MYOM2 [NCBI] 1.17029e-05
LMNA [NCBI] 1.16478e-05
APTX [NCBI] 1.15162e-05
SURF4 [NCBI] 1.07933e-05
CLU [NCBI] 1.06943e-05
SOX10 [NCBI] 1.0528e-05
ITGAM [NCBI] 9.95135e-06
KCNA6 [NCBI] 9.89562e-06
PLP1 [NCBI] 9.87662e-06
NPBWR1 [NCBI] 9.31293e-06
BMPER [NCBI] 9.31293e-06
MANBA [NCBI] 9.31293e-06
GFRA3 [NCBI] 8.53489e-06
PLP2 [NCBI] 8.53489e-06
CNTNAP1 [NCBI] 8.53489e-06
NAB1 [NCBI] 8.24815e-06
VGF [NCBI] 8.24815e-06
PNPLA6 [NCBI] 8.24815e-06
FAM126A [NCBI] 8.24815e-06
NINJ1 [NCBI] 8.0028e-06
PLXDC1 [NCBI] 8.0028e-06
NAB2 [NCBI] 8.0028e-06
PICK1 [NCBI] 7.78839e-06
ARF6 [NCBI] 7.78839e-06
PXMP2 [NCBI] 7.78839e-06
CLDN11 [NCBI] 7.78839e-06
CACNA1B [NCBI] 7.78839e-06
RPL27 [NCBI] 7.78839e-06
OPRL1 [NCBI] 7.77397e-06
KIF5A [NCBI] 7.598e-06
MPV17 [NCBI] 7.598e-06
PRPS1 [NCBI] 7.598e-06
ADAM22 [NCBI] 7.598e-06
MAD2L1BP [NCBI] 7.598e-06
KCNA2 [NCBI] 7.598e-06
ARTN [NCBI] 7.42679e-06
HSN2 [NCBI] 7.42679e-06
PARK2 [NCBI] 7.3983e-06
POU3F1 [NCBI] 7.27127e-06
PRX [NCBI] 7.27127e-06
GRM5 [NCBI] 7.22651e-06
SCN11A [NCBI] 7.12881e-06
CUGBP2 [NCBI] 7.12881e-06
SLC12A6 [NCBI] 6.87543e-06
PLEKHG4 [NCBI] 6.87543e-06
BMP5 [NCBI] 6.65507e-06
ASNS [NCBI] 6.65507e-06
JAM3 [NCBI] 6.5548e-06
SCARB2 [NCBI] 6.46015e-06
ATP6 [NCBI] 6.37053e-06
HPX [NCBI] 6.37053e-06
FMR1 [NCBI] 6.16982e-06
DNM2 [NCBI] 6.05327e-06
GAL [NCBI] 6.05327e-06
ICOSLG [NCBI] 6.05327e-06
BMP3 [NCBI] 5.9825e-06
ND2 [NCBI] 5.9825e-06
MAP1B [NCBI] 5.9825e-06
RTN4 [NCBI] 5.78652e-06
XK [NCBI] 5.72598e-06
ICOS [NCBI] 5.66755e-06
GAPDH [NCBI] 5.4568e-06
EMD [NCBI] 5.45238e-06
MYOT [NCBI] 5.3544e-06
TRPM8 [NCBI] 5.3075e-06
ITGA6 [NCBI] 5.26188e-06
HSPB8 [NCBI] 5.21748e-06
ND1 [NCBI] 5.13211e-06
RAG1 [NCBI] 5.11706e-06
GDAP1 [NCBI] 5.05094e-06
BSCL2 [NCBI] 5.05094e-06
ATF4 [NCBI] 5.0118e-06
EGR2 [NCBI] 5.0118e-06
CCK [NCBI] 4.92263e-06
MFN2 [NCBI] 4.86393e-06
AIF1 [NCBI] 4.82896e-06
AAAS [NCBI] 4.82896e-06
ELAVL4 [NCBI] 4.63346e-06
NAGA [NCBI] 4.54384e-06
CDR1 [NCBI] 4.51503e-06
ATF3 [NCBI] 4.43155e-06
ITGB4 [NCBI] 4.30133e-06
KCNQ2 [NCBI] 4.20422e-06
HMBS [NCBI] 4.20422e-06
REN [NCBI] 4.18083e-06
LAMA1 [NCBI] 4.18083e-06
THBD [NCBI] 4.13506e-06
LIFR [NCBI] 4.06876e-06
NEFM [NCBI] 4.04726e-06
ARSA [NCBI] 4.04726e-06
EPO [NCBI] 4.02897e-06
SLC22A5 [NCBI] 3.57127e-06
PTGER1 [NCBI] 3.57127e-06
TGM1 [NCBI] 3.5246e-06
NID1 [NCBI] 3.46449e-06
TGM2 [NCBI] 3.43528e-06
CD163 [NCBI] 3.43528e-06
MSTN [NCBI] 3.40662e-06
KCNJ8 [NCBI] 3.40662e-06
RELN [NCBI] 3.21973e-06
AGER [NCBI] 3.11068e-06
APOE [NCBI] 3.05253e-06
NGFR [NCBI] 3.04214e-06
FAH [NCBI] 3.00901e-06
CST3 [NCBI] 2.95585e-06
TLR3 [NCBI] 2.93445e-06
PARK7 [NCBI] 2.67781e-06
MAP2 [NCBI] 2.67781e-06
GSTP1 [NCBI] 2.62206e-06
ABCC2 [NCBI] 2.60145e-06
APOA1 [NCBI] 2.53684e-06
CD22 [NCBI] 2.52897e-06
VIP [NCBI] 2.50344e-06
GHRL [NCBI] 2.40864e-06
LYN [NCBI] 2.33839e-06
BMP4 [NCBI] 2.32476e-06
CYP2E1 [NCBI] 2.2979e-06
DAG1 [NCBI] 2.19545e-06
IL6ST [NCBI] 2.1893e-06
DDIT3 [NCBI] 2.1893e-06
CCL5 [NCBI] 2.14107e-06
FXN [NCBI] 2.08314e-06
TJP1 [NCBI] 2.0551e-06
FOLH1 [NCBI] 2.02764e-06
CD4 [NCBI] 2.02222e-06
SERPINF1 [NCBI] 1.99545e-06
SLC6A3 [NCBI] 1.87897e-06
AFP [NCBI] 1.87198e-06
SLC2A4 [NCBI] 1.83615e-06
TH [NCBI] 1.80129e-06
HFE [NCBI] 1.77234e-06
TNF [NCBI] 1.7506e-06
CHGA [NCBI] 1.67008e-06
CYP1A1 [NCBI] 1.44743e-06
CCR2 [NCBI] 1.31115e-06
HGF [NCBI] 1.16667e-06
ABCB1 [NCBI] 1.14622e-06
TROVE2 [NCBI] 1.09191e-06
PTK2 [NCBI] 1.04278e-06
BMP2 [NCBI] 1.0405e-06
ACP5 [NCBI] 9.35286e-07
MOG [NCBI] 8.67097e-07
GJB2 [NCBI] 8.57785e-07
GSTT1 [NCBI] 7.21742e-07
CCL2 [NCBI] 7.00211e-07
PTGS1 [NCBI] 6.80767e-07
IL1B [NCBI] 6.58965e-07
VWF [NCBI] 6.25331e-07
CXCL12 [NCBI] 5.93463e-07
EGF [NCBI] 5.48957e-07
JAK2 [NCBI] 5.26832e-07
GSTM1 [NCBI] 5.18696e-07
VEGFA [NCBI] 4.43205e-07
SOD1 [NCBI] 2.96021e-07
BCL2L1 [NCBI] 2.34547e-07
IL6 [NCBI] 1.8387e-07
CASP3 [NCBI] 1.37513e-07
HIF1A [NCBI] 5.95137e-08
PTH [NCBI] 9.39691e-09
PTGS2 [NCBI] 8.84356e-09
EGFR [NCBI] 6.75256e-09
BAX [NCBI] 6.99638e-11



OMIM


 OMIM Link Information
gain		 01
MAG [NCBI] 0.00201636
TTR [NCBI] 0.00163345
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy [NCBI] 0.001612
erythrokeratodermia variabilis 3 [NCBI] 0.001612
HNPP [NCBI] 0.00157926
GAN1 [NCBI] 0.0013572
MBS [NCBI] 0.00130862
visceral neuropathy, familial, autosomal recessive [NCBI] 0.00116474
neuropathy, congenital, with arthrogryposis multiplex [NCBI] 0.000952205
PMP22 [NCBI] 0.000900829
PNPLA6 [NCBI] 0.000769326
CMT2G [NCBI] 0.000734606
SCA25 [NCBI] 0.000734606
spinocerebellar ataxia with rigidity and peripheral neuropathy [NCBI] 0.000734606
AMRF [NCBI] 0.000734606
opticocochleodentate degeneration [NCBI] 0.000734606
SCAR3 [NCBI] 0.000652698
auditory neuropathy, autosomal dominant, 1 [NCBI] 0.000652698
cowchock syndrome [NCBI] 0.000652698
CMT1B [NCBI] 0.000589157
NGFB [NCBI] 0.000557725
SPG23 [NCBI] 0.000503004
folic acid, transport defect involving [NCBI] 0.000461483
ACCPN [NCBI] 0.000421366
ALD [NCBI] 0.00038675
HSAN2 [NCBI] 0.000381322
achalasia, familial esophageal [NCBI] 0.000379617
sjogren syndrome [NCBI] 0.000379617
EAOH [NCBI] 0.000277555
hypertrophic neuropathy of dejerine-sottas [NCBI] 0.000273213
HNA [NCBI] 0.000203072
GAN [NCBI] 0.000202786
neuropathy, hereditary sensory, atypical [NCBI] 0.000188582
MPZ [NCBI] 0.00017972
SCAR1 [NCBI] 0.000178863
hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy [NCBI] 0.000157675
CMTX5 [NCBI] 0.000143733
PCWH [NCBI] 0.000143733
MNGIE [NCBI] 0.000141827
HSAN1 [NCBI] 0.000139554
HFM [NCBI] 0.000135589
NN [NCBI] 0.000120934
RA [NCBI] 0.000119375
amyloidosis vii [NCBI] 0.000104468
lipomatosis, familial benign cervical [NCBI] 0.000101417
charcot-marie-tooth disease, axonal, type 2h [NCBI] 9.42604e-05
necrotizing encephalomyelopathy, subacute, of leigh, adult [NCBI] 9.42604e-05
hypertrophic neuropathy and cataract [NCBI] 9.42604e-05
neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [NCBI] 9.42604e-05
neurologic disease, infantile multisystem, with osseous fragility [NCBI] 9.42604e-05
myotilinopathy [NCBI] 9.42604e-05
cerebellar ataxia, benign, with thermoanalgesia [NCBI] 9.42604e-05
neuropathy, hereditary thermosensitive [NCBI] 9.42604e-05
peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain [NCBI] 9.42604e-05
laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy [NCBI] 9.42604e-05
ABCD1 [NCBI] 9.27466e-05
GJB3 [NCBI] 9.10854e-05
amyloidosis v [NCBI] 8.75664e-05
GJB1 [NCBI] 8.22461e-05
AAA [NCBI] 7.80466e-05
BDNF [NCBI] 7.25091e-05
hypomyelination and congenital cataract [NCBI] 7.18361e-05
spinal muscular atrophy, scapuloperoneal [NCBI] 7.18361e-05
cataract-ataxia-deafness-retardation syndrome [NCBI] 7.18361e-05
cerebrotendinous xanthomatosis [NCBI] 6.97652e-05
AD [NCBI] 6.88048e-05
EGF [NCBI] 6.8764e-05
KLK3 [NCBI] 6.48884e-05
krabbe disease [NCBI] 6.0094e-05
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [NCBI] 5.79423e-05
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy [NCBI] 5.79423e-05
HSAN3 [NCBI] 5.60252e-05
schindler disease, type i [NCBI] 5.38947e-05
SOX10 [NCBI] 5.15526e-05
KSS [NCBI] 5.08035e-05
TRPV1 [NCBI] 4.92799e-05
kanzaki disease [NCBI] 4.80128e-05
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome [NCBI] 4.80128e-05
ADAM22 [NCBI] 4.63751e-05
SCARB2 [NCBI] 4.63751e-05
JAM3 [NCBI] 4.63751e-05
DRP2 [NCBI] 4.63751e-05
APBD [NCBI] 4.57374e-05
corpus callosum, agenesis of [NCBI] 4.37542e-05
spinal muscular atrophy, proximal, adult, autosomal dominant [NCBI] 4.37542e-05
CMT4C [NCBI] 4.19976e-05
PTH [NCBI] 4.13175e-05
NAB1 [NCBI] 4.11971e-05
SLC12A6 [NCBI] 4.11971e-05
SMA4 [NCBI] 4.04222e-05
sea-blue histiocyte disease [NCBI] 4.04222e-05
de sanctis-cacchione syndrome [NCBI] 4.04222e-05
CMT2A2 [NCBI] 4.04222e-05
thyrotropin deficiency, isolated [NCBI] 3.89948e-05
SH3TC2 [NCBI] 3.78428e-05
ARF6 [NCBI] 3.78428e-05
congenital cataracts, facial dysmorphism, and neuropathy [NCBI] 3.76907e-05
CMT2A1 [NCBI] 3.76907e-05
VEGF [NCBI] 3.72872e-05
phosphoglycerate kinase 1 deficiency [NCBI] 3.64908e-05
HMN5 [NCBI] 3.64908e-05
SACS [NCBI] 3.64908e-05
MTTW [NCBI] 3.53545e-05
mannosidosis, beta a, lysosomal [NCBI] 3.43471e-05
TNF [NCBI] 3.41739e-05
GFAP [NCBI] 3.38432e-05
CFTD [NCBI] 3.33817e-05
neuropathy, congenital hypomyelinating [NCBI] 3.33817e-05
MPV17 [NCBI] 3.33763e-05
CNTF [NCBI] 3.3013e-05
INAD1 [NCBI] 3.24759e-05
myeloma, multiple [NCBI] 3.24759e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 3.24759e-05
EGFR [NCBI] 3.22897e-05
TTID [NCBI] 3.03337e-05
PRPS1 [NCBI] 3.03337e-05
SPG2 [NCBI] 3.00554e-05
MJD [NCBI] 2.98242e-05
SACS [NCBI] 2.91113e-05
MDC1A [NCBI] 2.86428e-05
RELA [NCBI] 2.8028e-05
CRC [NCBI] 2.78335e-05
niemann-pick disease, type b [NCBI] 2.73589e-05
CXCL13 [NCBI] 2.70557e-05
VWM [NCBI] 2.67586e-05
LMNA [NCBI] 2.60419e-05
CD [NCBI] 2.5815e-05
HPX [NCBI] 2.53683e-05
alkaptonuria [NCBI] 2.51005e-05
PRX [NCBI] 2.46263e-05
SMAX1 [NCBI] 2.42224e-05
AHC [NCBI] 2.3623e-05
EKV [NCBI] 2.3623e-05
PARK2 [NCBI] 2.31647e-05
FPLD2 [NCBI] 2.27217e-05
TGD [NCBI] 2.22932e-05
thrombocytopenic purpura, autoimmune [NCBI] 2.20121e-05
CMTX1 [NCBI] 2.18784e-05
CHAC [NCBI] 2.14764e-05
CADASIL [NCBI] 2.10866e-05
EMD [NCBI] 2.01866e-05
LIP [NCBI] 1.9984e-05
APTX [NCBI] 1.9758e-05
GDNF [NCBI] 1.97258e-05
PTK2B [NCBI] 1.89583e-05
ACHE [NCBI] 1.89416e-05
XPA [NCBI] 1.86505e-05
SLC18A2 [NCBI] 1.8584e-05
NF1 [NCBI] 1.85248e-05
CJD [NCBI] 1.81632e-05
TLR3 [NCBI] 1.72292e-05
AKR1B1 [NCBI] 1.72152e-05
ATF3 [NCBI] 1.69212e-05
REN [NCBI] 1.6624e-05
EDMD [NCBI] 1.66208e-05
CSA [NCBI] 1.63574e-05
neuraminidase deficiency [NCBI] 1.63574e-05
MTTK [NCBI] 1.63367e-05
MG [NCBI] 1.57519e-05
MTM1 [NCBI] 1.56017e-05
GLA [NCBI] 1.55293e-05
OPRM1 [NCBI] 1.55293e-05
PGK1 [NCBI] 1.50314e-05
coproporphyria [NCBI] 1.47932e-05
MHS1 [NCBI] 1.44452e-05
porphyria, acute intermittent [NCBI] 1.44452e-05
ABL [NCBI] 1.44452e-05
NF2 [NCBI] 1.38057e-05
AMC [NCBI] 1.28189e-05
CMT1A [NCBI] 1.28189e-05
PLP1 [NCBI] 1.18743e-05
porphyria variegata [NCBI] 1.15803e-05
metachromatic leukodystrophy [NCBI] 1.15803e-05
temporal arteritis [NCBI] 1.14423e-05
MBP [NCBI] 1.14314e-05
SLS [NCBI] 1.07827e-05
RDT [NCBI] 1.04816e-05
ARSA [NCBI] 1.00169e-05
tyrosinemia, type i [NCBI] 1.00169e-05
PD [NCBI] 9.89502e-06
NGFR [NCBI] 8.85897e-06
AFP [NCBI] 6.94455e-06
AVP [NCBI] 6.85522e-06
GAPDH [NCBI] 6.67535e-06
fabry disease [NCBI] 6.35375e-06
ZS [NCBI] 6.26593e-06
NPY [NCBI] 6.14714e-06
GAL [NCBI] 5.87004e-06
PWS [NCBI] 5.33452e-06
PMD [NCBI] 5.22124e-06
OPMD [NCBI] 5.14777e-06
ADCYAP1 [NCBI] 4.71289e-06
HGF [NCBI] 4.30491e-06
TNFSF6 [NCBI] 3.85278e-06
PEDF [NCBI] 3.70236e-06
APOE [NCBI] 3.24905e-06
RNASE3 [NCBI] 3.18702e-06
DMD [NCBI] 2.3335e-06
TH [NCBI] 1.99105e-06
EPO [NCBI] 1.86549e-06
CHS [NCBI] 1.79967e-06
PI [NCBI] 9.27311e-07
SPP1 [NCBI] 7.95173e-07
CCK [NCBI] 3.3647e-07
SLE [NCBI] 2.93901e-07
MUC1 [NCBI] 1.46478e-07
VIP [NCBI] 1.39452e-07
PTK2 [NCBI] 4.59505e-08
CVID [NCBI] 5.08908e-09
AT [NCBI] 1.53996e-09



Database Center for Life Science