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01 Dysarthria [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000439573
ADSD [NCBI] 0.000332969
SPOAN [NCBI] 0.000332969
SCAX1 [NCBI] 0.000332969
SACS [NCBI] 2.29279e-05
KCNA1 [NCBI] 2.14488e-05
POLG [NCBI] 1.81707e-05
ZFP90 [NCBI] 1.75558e-05
CACNA1A [NCBI] 1.52362e-05
ZFYVE26 [NCBI] 1.36935e-05
MECP2 [NCBI] 1.33392e-05
SYNE1 [NCBI] 1.19741e-05
NDUFS8 [NCBI] 1.18022e-05
PEX12 [NCBI] 1.15027e-05
PAK3 [NCBI] 1.11333e-05
ATP1A3 [NCBI] 1.11333e-05
ATP6 [NCBI] 1.07393e-05
SLC26A3 [NCBI] 9.71131e-06
C10orf2 [NCBI] 9.66367e-06
APTX [NCBI] 8.91458e-06
FOXP2 [NCBI] 8.85497e-06
ATP7B [NCBI] 7.75063e-06
GRN [NCBI] 7.661e-06
NPC1 [NCBI] 7.43e-06
CP [NCBI] 6.41048e-06
PSEN1 [NCBI] 6.30916e-06
DMPK [NCBI] 5.89309e-06
PRNP [NCBI] 5.77453e-06
HTT [NCBI] 4.47608e-06
JAK2 [NCBI] 4.26642e-06



OMIM


 OMIM Link Information
gain		 01
SPOAN [NCBI] 0.00106493
ADSD [NCBI] 0.00106493
AMRF [NCBI] 0.000847142
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome [NCBI] 0.000765046
SPG15 [NCBI] 0.000640751
SCAX1 [NCBI] 0.000614596
spinocerebellar ataxia 29 [NCBI] 0.000555363
epilepsy, myoclonic, benign adult familial, type 1 [NCBI] 0.000512699
DYT2 [NCBI] 0.000500764
IBGC1 [NCBI] 0.00042895
palatopharyngeal incompetence [NCBI] 0.00034423
PD [NCBI] 0.000263779
fitzsimmons-guilbert syndrome [NCBI] 0.000228269
SANDO [NCBI] 0.000191357
BPP [NCBI] 0.000178142
SACS [NCBI] 0.000145268
suprabulbar paresis, congenital [NCBI] 0.000106872
geographic tongue and fissured tongue [NCBI] 9.83952e-05
pachygyria with mental retardation and seizures [NCBI] 9.28923e-05
branchial myoclonus with spastic paraparesis and cerebellar ataxia [NCBI] 8.88018e-05
NDUFS8 [NCBI] 7.67933e-05
SACS [NCBI] 7.10121e-05
MJD [NCBI] 7.03563e-05
EA1 [NCBI] 6.87826e-05
aceruloplasminemia [NCBI] 6.87826e-05
glutaric acidemia i [NCBI] 6.593e-05
PEX12 [NCBI] 6.45705e-05
C10ORF2 [NCBI] 6.34643e-05
GSD [NCBI] 6.27781e-05
alzheimer disease 3 [NCBI] 5.89784e-05
FHM1 [NCBI] 5.73722e-05
MTATP6 [NCBI] 4.93128e-05
ATP7B [NCBI] 4.90649e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 4.89054e-05
metachromatic leukodystrophy [NCBI] 4.34419e-05
JAK2 [NCBI] 4.05713e-05
CP [NCBI] 3.2154e-05
HD [NCBI] 2.17834e-05
ALD [NCBI] 1.73298e-05
temporal arteritis [NCBI] 1.61224e-05
CJD [NCBI] 5.60992e-06
MG [NCBI] 2.58113e-06
AD [NCBI] 2.70011e-07



Database Center for Life Science