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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hereditary Sensory and Motor Neuropathy [NCBI]


Gene


Gene Link Information
Gain
01
PMP22 [NCBI] 0.00110045
CDRT15P [NCBI] 0.000362052
CDRT12 [NCBI] 0.000362052
CDRT8 [NCBI] 0.000362052
CDRT10 [NCBI] 0.000362052
SMAN1 [NCBI] 0.000362052
CDRT13 [NCBI] 0.000362052
CDRT7 [NCBI] 0.000362052
CDRT5 [NCBI] 0.000362052
CDRT2 [NCBI] 0.000362052
SPOAN [NCBI] 0.000362052
HMSNO [NCBI] 0.000362052
CDRT14 [NCBI] 0.000362052
CMT2C [NCBI] 0.000362052
CDRT11 [NCBI] 0.000362052
CDRT3 [NCBI] 0.000362052
HMNJ [NCBI] 0.000362052
CMTX3 [NCBI] 0.000301317
MPZ [NCBI] 0.000249687
GJB1 [NCBI] 0.000117991
BSCL2 [NCBI] 6.89289e-05
HSPB8 [NCBI] 5.84197e-05
HSPB1 [NCBI] 4.49778e-05
MS [NCBI] 4.00447e-05
EGR2 [NCBI] 3.50652e-05
CDRT1 [NCBI] 3.19521e-05
GER [NCBI] 3.06177e-05
MAD2L1BP [NCBI] 2.04248e-05
POLG [NCBI] 2.01808e-05
HSN2 [NCBI] 2.0062e-05
SLC12A6 [NCBI] 1.89051e-05
GAN [NCBI] 1.89051e-05
NEFL [NCBI] 1.72599e-05
SEPT9 [NCBI] 1.65275e-05
NDRG1 [NCBI] 1.60702e-05
CDRT15 [NCBI] 1.45026e-05
CDRT4 [NCBI] 1.45026e-05
DDX23 [NCBI] 1.45026e-05
CDRT9 [NCBI] 1.45026e-05
ZFP90 [NCBI] 1.45026e-05
TEKT3 [NCBI] 1.21224e-05
TTR [NCBI] 1.1936e-05
ARF3 [NCBI] 1.06412e-05
SLA [NCBI] 1.02077e-05
NDRG3 [NCBI] 1.02077e-05
HADHB [NCBI] 9.86226e-06
CLIP2 [NCBI] 9.86226e-06
TNRC6A [NCBI] 9.57509e-06
NINJ1 [NCBI] 9.32931e-06
HSPB6 [NCBI] 9.32931e-06
DHH [NCBI] 9.32931e-06
CCT5 [NCBI] 9.11447e-06
PXMP2 [NCBI] 9.11447e-06
TUBA1C [NCBI] 9.11447e-06
MAGI2 [NCBI] 8.92365e-06
PRX [NCBI] 8.59606e-06
SH3TC2 [NCBI] 8.59606e-06
GPR109B [NCBI] 8.45316e-06
PTPN12 [NCBI] 8.32131e-06
SPG20 [NCBI] 8.19892e-06
CKB [NCBI] 8.19892e-06
PRPH [NCBI] 8.08472e-06
COX10 [NCBI] 7.877e-06
NDRG2 [NCBI] 7.78192e-06
SPTLC1 [NCBI] 7.78192e-06
DCTN1 [NCBI] 7.78192e-06
ATP6 [NCBI] 7.69186e-06
HADHA [NCBI] 7.60634e-06
SETX [NCBI] 7.5249e-06
LITAF [NCBI] 7.44719e-06
ICOSLG [NCBI] 7.37288e-06
PNMA2 [NCBI] 7.30168e-06
MTMR2 [NCBI] 7.23334e-06
IGHMBP2 [NCBI] 7.1044e-06
WISP1 [NCBI] 7.1044e-06
ICOS [NCBI] 6.98457e-06
ATL1 [NCBI] 6.53062e-06
IKBKAP [NCBI] 6.40287e-06
HIP1 [NCBI] 6.24632e-06
MFN2 [NCBI] 6.17319e-06
RAB7A [NCBI] 5.90884e-06
GCH1 [NCBI] 5.7908e-06
AMACR [NCBI] 5.62803e-06
REN [NCBI] 5.47973e-06
OPA1 [NCBI] 4.97404e-06
MB [NCBI] 4.45551e-06
SPAST [NCBI] 4.40553e-06
ATXN3 [NCBI] 3.74841e-06
LMNA [NCBI] 3.34163e-06
MBP [NCBI] 3.18392e-06
PRNP [NCBI] 2.83019e-06
TG [NCBI] 1.19932e-06
AR [NCBI] 3.83944e-07
GFAP [NCBI] 3.83115e-07
NGF [NCBI] 3.38131e-07




OMIM


OMIM Link Information
gain
01
neuropathy, hereditary motor and sensory, okinawa type [NCBI] 0.00257456
hypertrophic neuropathy of dejerine-sottas [NCBI] 0.00202988
neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [NCBI] 0.00194338
PMP22 [NCBI] 0.00169371
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers [NCBI] 0.00164346
hereditary motor and sensory neuropathy, type iic [NCBI] 0.00134416
HMN1 [NCBI] 0.00128649
MPZ [NCBI] 0.00119314
polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive [NCBI] 0.00096756
SPOAN [NCBI] 0.00096756
DSMA2 [NCBI] 0.00096756
HNPP [NCBI] 0.00095858
RDPA [NCBI] 0.000749926
spastic diplegia, infantile type [NCBI] 0.000749926
cowchock syndrome [NCBI] 0.000667984
DSMA3 [NCBI] 0.000614885
neuropathy, hereditary motor and sensory, russe type [NCBI] 0.000518153
neuropathy, congenital hypomyelinating [NCBI] 0.000484779
MTND4 [NCBI] 0.000472004
CMT4D [NCBI] 0.000440228
leber optic atrophy, susceptibility to [NCBI] 0.00039449
leber optic atrophy [NCBI] 0.000354144
CMT1B [NCBI] 0.000353461
CMT1A [NCBI] 0.000334132
hereditary motor and sensory neuropathy vi [NCBI] 0.00027649
GJB1 [NCBI] 0.000222191
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [NCBI] 0.000175595
HMN2A [NCBI] 0.000139529
EGR2 [NCBI] 0.0001359
spastic paraplegia with neuropathy and poikiloderma [NCBI] 0.00011017
HMN2B [NCBI] 0.00011017
neuropathy, hereditary thermosensitive [NCBI] 0.00011017
optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant [NCBI] 0.00011017
charcot-marie-tooth disease, dominant intermediate d [NCBI] 0.00011017
GAN1 [NCBI] 0.00010794
GAN [NCBI] 0.000107409
CMTX1 [NCBI] 9.58991e-05
NDRG1 [NCBI] 9.56559e-05
SPG3A [NCBI] 9.24613e-05
slowed nerve conduction velocity, autosomal dominant [NCBI] 8.77159e-05
HSPB1 [NCBI] 8.30345e-05
charcot-marie-tooth disease, axonal, type 2f [NCBI] 7.92517e-05
keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy [NCBI] 7.92517e-05
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy [NCBI] 7.37614e-05
NDRG3 [NCBI] 7.26222e-05
SLA [NCBI] 7.26222e-05
CCT5 [NCBI] 7.26222e-05
ARHGEF10 [NCBI] 7.26222e-05
TNRC6A [NCBI] 7.26222e-05
bile acid synthesis defect, congenital, 4 [NCBI] 6.96835e-05
charcot-marie-tooth disease, axonal, type 2j [NCBI] 6.64375e-05
SANDO [NCBI] 6.37411e-05
NN [NCBI] 6.37411e-05
ALS4 [NCBI] 6.37411e-05
CMT4B1 [NCBI] 6.14354e-05
CMT4B2 [NCBI] 5.94218e-05
NDRG2 [NCBI] 5.88481e-05
HAM [NCBI] 5.7635e-05
TTR [NCBI] 5.72481e-05
SPG17 [NCBI] 5.60292e-05
trifunctional protein deficiency [NCBI] 5.45716e-05
ARF3 [NCBI] 5.36533e-05
TST [NCBI] 5.36533e-05
NINJ1 [NCBI] 5.36533e-05
ACCPN [NCBI] 5.32371e-05
HMN5 [NCBI] 5.2007e-05
DSMA1 [NCBI] 5.08662e-05
COX10 [NCBI] 4.7777e-05
HSPB8 [NCBI] 4.5782e-05
SBF2 [NCBI] 4.5782e-05
SPG2 [NCBI] 4.53595e-05
EAOH [NCBI] 4.38862e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 4.38862e-05
AAA [NCBI] 4.31993e-05
HNA [NCBI] 4.31993e-05
PRPH [NCBI] 4.27058e-05
IGHMBP2 [NCBI] 4.14666e-05
BSCL2 [NCBI] 4.03664e-05
CGL2 [NCBI] 4.0162e-05
PRX [NCBI] 3.68976e-05
HADHA [NCBI] 3.61936e-05
MAG [NCBI] 3.48507e-05
ATXN8OS [NCBI] 3.06535e-05
GCH1 [NCBI] 2.99161e-05
REN [NCBI] 2.85926e-05
GSN [NCBI] 2.82886e-05
POLG [NCBI] 2.66442e-05
MTATP6 [NCBI] 2.63959e-05
AMACR [NCBI] 2.44152e-05
NS1 [NCBI] 2.14689e-05
MB [NCBI] 1.57715e-05
dystrophia myotonica 1 [NCBI] 9.71884e-06
MJD [NCBI] 8.48476e-06
MBP [NCBI] 3.25918e-06
GFAP [NCBI] 8.43455e-07
TG [NCBI] 5.38888e-07
AR [NCBI] 1.98695e-07




Database Center for Life Science