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01 Learning Disorders [NCBI]


Gene


Gene Link Information
Gain
01
MRX49 [NCBI] 0.000284409
DGCR [NCBI] 0.000261497
VCF [NCBI] 0.000246623
DYX1 [NCBI] 0.000207698
TRNL1 [NCBI] 0.000133816
MS [NCBI] 0.000121158
GTS [NCBI] 0.00010534
CHAT [NCBI] 9.95356e-05
NSD1 [NCBI] 5.72393e-05
ACHE [NCBI] 3.27491e-05
BDNF [NCBI] 2.10782e-05
FMR1 [NCBI] 1.79308e-05
WIZ [NCBI] 1.52544e-05
TH [NCBI] 1.50689e-05
MRPL40 [NCBI] 1.19759e-05
GRM5 [NCBI] 1.12867e-05
ST8SIA4 [NCBI] 1.0959e-05
NPAS3 [NCBI] 1.0959e-05
DRD4 [NCBI] 1.08328e-05
CRBN [NCBI] 1.06135e-05
RCAN2 [NCBI] 1.03262e-05
CTBP2 [NCBI] 1.00802e-05
SLC6A3 [NCBI] 9.90681e-06
APOE [NCBI] 9.85733e-06
LEMD3 [NCBI] 8.94893e-06
DYX1C1 [NCBI] 8.72745e-06
KIAA0319 [NCBI] 8.44123e-06
APP [NCBI] 8.34511e-06
DLG4 [NCBI] 8.19616e-06
RAI1 [NCBI] 8.19616e-06
SYP [NCBI] 8.12172e-06
GCLC [NCBI] 8.12172e-06
NAGS [NCBI] 7.98192e-06
SIM2 [NCBI] 7.91609e-06
CLN5 [NCBI] 7.91609e-06
CNTN2 [NCBI] 7.85272e-06
GDI1 [NCBI] 7.79161e-06
FXR1 [NCBI] 7.79161e-06
BBS1 [NCBI] 7.67561e-06
TPH2 [NCBI] 7.56701e-06
MCPH1 [NCBI] 7.46493e-06
DBI [NCBI] 7.03021e-06
NGF [NCBI] 6.96495e-06
TPH1 [NCBI] 6.59317e-06
FOXP2 [NCBI] 6.5638e-06
ARX [NCBI] 6.45117e-06
PITX3 [NCBI] 6.29519e-06
KCNQ2 [NCBI] 6.24624e-06
NDP [NCBI] 6.24624e-06
ARSA [NCBI] 6.08534e-06
IDE [NCBI] 5.91854e-06
MARCKS [NCBI] 5.8035e-06
HTR1B [NCBI] 5.78507e-06
PAFAH1B1 [NCBI] 5.62777e-06
UBE3A [NCBI] 5.49939e-06
GRN [NCBI] 5.3802e-06
CREB1 [NCBI] 5.36589e-06
MAOA [NCBI] 5.2556e-06
EPB41L1 [NCBI] 5.22914e-06
KCNJ11 [NCBI] 5.19022e-06
PSAP [NCBI] 5.19022e-06
SST [NCBI] 5.06674e-06
NF1 [NCBI] 5.05488e-06
EPB41L2 [NCBI] 5.05488e-06
DBH [NCBI] 5.05488e-06
PTN [NCBI] 4.9298e-06
PTEN [NCBI] 4.76658e-06
OPRL1 [NCBI] 4.74367e-06
MAP2 [NCBI] 4.65797e-06
ATXN1 [NCBI] 4.5854e-06
NPY [NCBI] 4.57207e-06
TOR1A [NCBI] 4.50744e-06
CDK5 [NCBI] 4.47396e-06
GNAS [NCBI] 4.425e-06
PYY [NCBI] 4.409e-06
DRD2 [NCBI] 4.1725e-06
FOXO1 [NCBI] 4.16564e-06
DMPK [NCBI] 3.64992e-06
CNTF [NCBI] 3.62054e-06
GFAP [NCBI] 3.56657e-06
PRKCB [NCBI] 3.45504e-06
INS [NCBI] 3.44634e-06
MECP2 [NCBI] 3.23597e-06
SLC2A1 [NCBI] 3.17304e-06
MAPT [NCBI] 2.77717e-06
COMT [NCBI] 2.7661e-06
GJB2 [NCBI] 2.57526e-06
SLC6A4 [NCBI] 2.53244e-06
SNCA [NCBI] 2.05894e-06
VIP [NCBI] 1.98643e-06
BCL2L1 [NCBI] 1.63569e-06
HGF [NCBI] 1.20501e-06
EPO [NCBI] 7.90406e-07
TNF [NCBI] 1.99849e-08




OMIM


OMIM Link Information
gain
01
centralopathic epilepsy [NCBI] 0.00118764
intelligence quantitative trait locus 2 [NCBI] 0.00102539
intelligence quantitative trait locus 3 [NCBI] 0.00102539
cayler cardiofacial syndrome [NCBI] 0.00101328
SPG9 [NCBI] 0.000725612
velocardiofacial syndrome [NCBI] 0.000662821
microcephaly, autosomal dominant [NCBI] 0.000486675
SRS [NCBI] 0.000476138
ADHD [NCBI] 0.000459523
MRX1 [NCBI] 0.000431005
GTS [NCBI] 0.000426214
CHAT [NCBI] 0.000377989
DYX1 [NCBI] 0.00025583
kabuki syndrome [NCBI] 0.000254316
TS [NCBI] 0.000149412
sotos syndrome [NCBI] 0.000147413
feingold syndrome [NCBI] 0.000128683
NF1 [NCBI] 0.000114518
COH1 [NCBI] 9.34894e-05
ACHE [NCBI] 9.32441e-05
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [NCBI] 8.94311e-05
epilepsy, myoclonic, x-linked, with mental retardation and spasticity [NCBI] 8.94311e-05
suprabulbar paresis, congenital [NCBI] 8.94311e-05
apnea, obstructive sleep [NCBI] 8.93973e-05
yemenite deaf-blind hypopigmentation syndrome [NCBI] 8.09651e-05
MRT2 [NCBI] 7.5473e-05
MRPL40 [NCBI] 7.36979e-05
SYNPO [NCBI] 7.36979e-05
CPLX2 [NCBI] 7.36979e-05
subglottic bar [NCBI] 7.13933e-05
FMR1 [NCBI] 7.01572e-05
chromosome 18p deletion syndrome [NCBI] 6.81454e-05
gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to [NCBI] 6.54472e-05
THRB [NCBI] 6.51356e-05
corpus callosum, agenesis of [NCBI] 6.11243e-05
ADRA2A [NCBI] 5.99231e-05
GRM5 [NCBI] 5.99231e-05
CRBN [NCBI] 5.99231e-05
GCLC [NCBI] 5.99231e-05
SCZD4 [NCBI] 5.7728e-05
BDNF [NCBI] 5.6635e-05
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 5.37003e-05
GRTH [NCBI] 5.25576e-05
CTHM [NCBI] 5.25576e-05
DYX2 [NCBI] 5.14924e-05
DLG4 [NCBI] 5.13558e-05
GRM1 [NCBI] 5.13558e-05
galactose epimerase deficiency [NCBI] 5.04948e-05
HSR [NCBI] 4.51958e-05
chromosome 17q21.31 microdeletion syndrome [NCBI] 4.51958e-05
NAGS [NCBI] 4.51958e-05
CLN1 [NCBI] 4.35826e-05
histidinemia [NCBI] 4.29751e-05
SIM2 [NCBI] 4.25369e-05
PAK3 [NCBI] 4.1436e-05
autonomic control, congenital failure of [NCBI] 4.02541e-05
PKS [NCBI] 3.97637e-05
SYP [NCBI] 3.95472e-05
CADASIL [NCBI] 3.75249e-05
NSD1 [NCBI] 3.59867e-05
TBX1 [NCBI] 3.59867e-05
UBE3A [NCBI] 3.54076e-05
PWS [NCBI] 3.45962e-05
TH [NCBI] 3.37678e-05
DYT1 [NCBI] 3.23136e-05
SOX10 [NCBI] 3.21039e-05
CTNS [NCBI] 3.2024e-05
AS [NCBI] 3.13633e-05
ARX [NCBI] 3.06242e-05
LKS [NCBI] 3.01443e-05
SLC6A3 [NCBI] 2.86087e-05
ND [NCBI] 2.8483e-05
DBI [NCBI] 2.65099e-05
COMT [NCBI] 2.59699e-05
IDE [NCBI] 2.34916e-05
KRAS [NCBI] 2.33319e-05
SLE [NCBI] 2.31577e-05
NS1 [NCBI] 2.3009e-05
ARSA [NCBI] 2.24276e-05
SMS [NCBI] 2.18605e-05
SNCA [NCBI] 2.17368e-05
APOE [NCBI] 2.09031e-05
MTTL1 [NCBI] 2.06119e-05
RASA1 [NCBI] 2.0266e-05
MS [NCBI] 1.99491e-05
BBS [NCBI] 1.91474e-05
CDK5 [NCBI] 1.81612e-05
TNF [NCBI] 1.77253e-05
SST [NCBI] 1.69173e-05
MAP2 [NCBI] 1.64661e-05
PTEN [NCBI] 1.58313e-05
PSEN1 [NCBI] 1.52412e-05
DGS [NCBI] 1.43001e-05
APP [NCBI] 1.42858e-05
WBS [NCBI] 1.31251e-05
PYY [NCBI] 1.23883e-05
phenylketonuria [NCBI] 1.12757e-05
CNTF [NCBI] 8.01638e-06
amyloidosis vi [NCBI] 7.51672e-06
NGFB [NCBI] 7.05356e-06
GDNF [NCBI] 4.73816e-06
NPY [NCBI] 4.47518e-06
ALD [NCBI] 4.45962e-06
MDD [NCBI] 2.27091e-06
FTD [NCBI] 1.66677e-06
GFAP [NCBI] 1.54468e-06
VIP [NCBI] 1.27983e-06
CD [NCBI] 1.07826e-06
AD [NCBI] 6.21914e-07
EPO [NCBI] 5.57746e-07
lymphoma, non-hodgkin, familial [NCBI] 3.83727e-07
HGF [NCBI] 2.905e-08




Database Center for Life Science