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01 Basal Ganglia Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
IBGC1 [NCBI] 0.000754986
ADSD [NCBI] 0.000373825
AGS2 [NCBI] 0.000313087
CYP2D6 [NCBI] 6.0172e-05
FTL [NCBI] 3.92095e-05
DRD2 [NCBI] 3.78946e-05
RNASEH2A [NCBI] 3.72436e-05
TREX1 [NCBI] 3.38081e-05
SLC6A3 [NCBI] 2.71414e-05
SLC19A3 [NCBI] 2.32083e-05
CHAT [NCBI] 2.21115e-05
TREM2 [NCBI] 2.02945e-05
TPI1 [NCBI] 1.99822e-05
VPS13A [NCBI] 1.94319e-05
TYROBP [NCBI] 1.76046e-05
MAPT [NCBI] 1.56545e-05
SNCA [NCBI] 1.33103e-05
TOR1A [NCBI] 1.26333e-05
KCNA6 [NCBI] 1.26105e-05
RNASEH2C [NCBI] 1.26105e-05
DRD4 [NCBI] 1.20919e-05
TH [NCBI] 1.17024e-05
MS [NCBI] 1.14177e-05
AP1S2 [NCBI] 1.12478e-05
ATP13A2 [NCBI] 1.07145e-05
KCNA2 [NCBI] 1.03084e-05
CYP3A4 [NCBI] 1.00295e-05
OPA3 [NCBI] 9.58263e-06
ATXN10 [NCBI] 9.361e-06
PACRG [NCBI] 9.2601e-06
IMPDH1 [NCBI] 8.54891e-06
GAMT [NCBI] 8.30814e-06
HTT [NCBI] 8.05278e-06
CA2 [NCBI] 8.00071e-06
KCNA1 [NCBI] 7.82279e-06
SNCB [NCBI] 7.74034e-06
DRD5 [NCBI] 7.70057e-06
SLC18A2 [NCBI] 7.25367e-06
HTR2C [NCBI] 7.19426e-06
FOXP2 [NCBI] 7.19426e-06
PRKCI [NCBI] 7.00132e-06
BDNF [NCBI] 6.59532e-06
DRD3 [NCBI] 6.58734e-06
PANK2 [NCBI] 6.48829e-06
ACHE [NCBI] 6.37365e-06
GATA3 [NCBI] 5.92178e-06
IL2RA [NCBI] 5.8677e-06
HTR2A [NCBI] 5.66732e-06
ATP7A [NCBI] 5.48841e-06
OGG1 [NCBI] 5.4569e-06
PINK1 [NCBI] 5.39562e-06
ATXN1 [NCBI] 5.20629e-06
NOTCH3 [NCBI] 5.02835e-06
NEFH [NCBI] 4.6057e-06
APOE [NCBI] 3.92306e-06
COMT [NCBI] 3.35865e-06
PARK2 [NCBI] 3.22588e-06
SLC6A4 [NCBI] 3.11822e-06
PTH [NCBI] 2.92466e-06
HRAS [NCBI] 2.2616e-06
AKT1 [NCBI] 1.68951e-06
PRL [NCBI] 1.07425e-06



OMIM


 OMIM Link Information
gain		 01
IBGC1 [NCBI] 0.00846324
basal ganglia calcification, idiopathic, childhood-onset [NCBI] 0.00361041
parkinsonism, early-onset, with mental retardation [NCBI] 0.00189724
basal ganglia calcification, idiopathic, 2 [NCBI] 0.00146205
ADSD [NCBI] 0.000945056
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome [NCBI] 0.000645584
EPV [NCBI] 0.000645584
dandy-walker malformation with mental retardation, basal ganglia disease, and seizures [NCBI] 0.000592537
AGS1 [NCBI] 0.000571954
NBIA1 [NCBI] 0.00046148
SNDI [NCBI] 0.000421922
spondyloenchondrodysplasia [NCBI] 0.000395299
FTD [NCBI] 0.000359902
basal ganglia disease, adult-onset [NCBI] 0.000269392
pena-shokeir syndrome, type i [NCBI] 0.000224582
basal ganglia disease, biotin-responsive [NCBI] 0.000224323
OPTB3 [NCBI] 0.000197432
RA [NCBI] 0.000185767
CHBL [NCBI] 0.00017941
FTL [NCBI] 0.000162151
EKD1 [NCBI] 0.000154933
SLE [NCBI] 0.000128301
SCA1 [NCBI] 0.000119859
TREX1 [NCBI] 0.00011706
AD [NCBI] 0.000114708
encephalopathy, recurrent, of childhood [NCBI] 0.00011207
AGS5 [NCBI] 0.00011207
apraxia of eyelid opening [NCBI] 0.00011207
schimke x-linked mental retardation syndrome [NCBI] 0.00011207
PSNP1 [NCBI] 0.000110404
GLUD1 [NCBI] 0.000109736
CHAT [NCBI] 9.5168e-05
AGS2 [NCBI] 8.9613e-05
karak syndrome [NCBI] 8.9613e-05
encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration [NCBI] 8.9613e-05
SLC19A3 [NCBI] 8.32422e-05
optic atrophy 3, autosomal dominant [NCBI] 8.11469e-05
MJD [NCBI] 7.52762e-05
MRX59 [NCBI] 7.15747e-05
RNASEH2B [NCBI] 6.94637e-05
RNASEH2C [NCBI] 6.94637e-05
TH [NCBI] 6.8354e-05
dystonia, familial, with visual failure and striatal lucencies [NCBI] 6.83266e-05
alpha-ketoglutarate dehydrogenase deficiency [NCBI] 6.42646e-05
GLUD2 [NCBI] 6.42646e-05
RNASEH2A [NCBI] 6.42646e-05
wilson disease [NCBI] 6.37093e-05
alzheimer disease, susceptibility to, mitochondrial [NCBI] 6.1305e-05
AP1S2 [NCBI] 6.0889e-05
spinocerebellar ataxia, 16q22-linked [NCBI] 5.79084e-05
antiphospholipid syndrome [NCBI] 5.64487e-05
TREM2 [NCBI] 5.47179e-05
DRPLA [NCBI] 5.36942e-05
SDHC [NCBI] 5.32952e-05
INAD1 [NCBI] 4.97359e-05
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 [NCBI] 4.88509e-05
PLOSL [NCBI] 4.80134e-05
MTCO2 [NCBI] 4.74606e-05
SCA10 [NCBI] 4.72185e-05
SLC6A8 [NCBI] 4.67522e-05
PPARGC1A [NCBI] 4.67522e-05
SCA17 [NCBI] 4.64623e-05
MTCO1 [NCBI] 4.43387e-05
DRD [NCBI] 4.25681e-05
biotinidase deficiency [NCBI] 4.25681e-05
TBP [NCBI] 4.24015e-05
GCDH [NCBI] 4.04178e-05
MCOPS7 [NCBI] 3.994e-05
GAMT [NCBI] 3.90767e-05
ODDD [NCBI] 3.85567e-05
SCA7 [NCBI] 3.13602e-05
SCZD [NCBI] 3.03155e-05
MAPT [NCBI] 2.66918e-05
SCA2 [NCBI] 2.63821e-05
ALS1 [NCBI] 2.58223e-05
LS [NCBI] 2.39465e-05
ACHE [NCBI] 2.11776e-05
KSS [NCBI] 1.68054e-05
SLC6A3 [NCBI] 1.6669e-05
leber optic atrophy [NCBI] 1.41602e-05
CHS [NCBI] 1.31407e-05
GDNF [NCBI] 1.23697e-05
HD [NCBI] 1.0329e-05
PD [NCBI] 9.27823e-06
BDNF [NCBI] 5.91395e-06
PTH [NCBI] 5.093e-06
GTS [NCBI] 4.95113e-06
APOE [NCBI] 2.42758e-06
MDD [NCBI] 2.35172e-06
panencephalitis, subacute sclerosing [NCBI] 1.56444e-06
PRL [NCBI] 9.09624e-07
CJD [NCBI] 8.47166e-08



Database Center for Life Science