MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Language Development Disorders
[NCBI]
Gene
Gene
Link
Information
Gain
01
SLI2
[NCBI]
0.000438875
SLI1
[NCBI]
0.000438875
DYX8
[NCBI]
0.000355204
FOXP2
[NCBI]
0.000169708
MECP2
[NCBI]
2.89689e-05
AUH
[NCBI]
2.66623e-05
SHANK3
[NCBI]
2.52611e-05
ALDH5A1
[NCBI]
1.91687e-05
GJB2
[NCBI]
1.80642e-05
APPL2
[NCBI]
1.69071e-05
UBE3A
[NCBI]
1.66971e-05
DPYS
[NCBI]
1.30448e-05
SHC2
[NCBI]
1.30448e-05
WHSC2
[NCBI]
1.19779e-05
CNTNAP2
[NCBI]
1.03777e-05
KIAA0319
[NCBI]
1.00911e-05
GRB10
[NCBI]
1.00053e-05
FMR1
[NCBI]
9.8581e-06
GAD1
[NCBI]
9.84556e-06
SLC6A8
[NCBI]
9.77097e-06
TCF4
[NCBI]
9.56491e-06
WHSC1
[NCBI]
9.26852e-06
CDH23
[NCBI]
9.16299e-06
MCPH1
[NCBI]
9.11257e-06
GATA4
[NCBI]
8.45971e-06
ZEB2
[NCBI]
8.32917e-06
MYO7A
[NCBI]
7.08984e-06
DMPK
[NCBI]
5.25384e-06
SHH
[NCBI]
5.24875e-06
NGF
[NCBI]
2.10066e-06
OMIM
OMIM
Link
Information
gain
01
SLI2
[NCBI]
0.00217885
SLI1
[NCBI]
0.00217885
autism
[NCBI]
0.00161388
hairy elbows
[NCBI]
0.00147237
AUTS10
[NCBI]
0.000862873
SLI3
[NCBI]
0.000862873
AUTS5
[NCBI]
0.00072749
AUTS4
[NCBI]
0.000656414
spinocerebellar ataxia 29
[NCBI]
0.000570957
floating-harbor syndrome
[NCBI]
0.000399401
SPCH1
[NCBI]
0.000339478
chromosome 22q13.3 deletion syndrome
[NCBI]
0.000271313
williams-beuren region duplication syndrome
[NCBI]
0.000253305
LKS
[NCBI]
0.000187098
SHANK3
[NCBI]
0.000148925
AUH
[NCBI]
0.000148925
MECP2
[NCBI]
0.000145863
FOXP2
[NCBI]
0.000136812
tetralogy of fallot syndrome, autosomal recessive
[NCBI]
0.000126428
speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe crease
[NCBI]
0.000126428
AS
[NCBI]
0.000105673
3-@methylglutaconic aciduria, type iv
[NCBI]
0.000103962
APPL2
[NCBI]
9.47785e-05
barber-say syndrome
[NCBI]
8.58948e-05
APPL1
[NCBI]
8.09985e-05
3-@methylglutaconic aciduria, type iii
[NCBI]
7.99294e-05
ablepharon-macrostomia syndrome
[NCBI]
7.55871e-05
WBS
[NCBI]
7.31627e-05
WZS
[NCBI]
6.93565e-05
3-@methylglutaconic aciduria, type i
[NCBI]
6.93565e-05
DYX2
[NCBI]
6.58876e-05
succinic semialdehyde dehydrogenase deficiency
[NCBI]
6.48803e-05
HADHA
[NCBI]
5.82665e-05
DYX1
[NCBI]
5.50112e-05
mucolipidosis iv
[NCBI]
5.44947e-05
COH1
[NCBI]
4.97112e-05
BTHS
[NCBI]
4.93408e-05
ADHD
[NCBI]
4.72855e-05
WHS
[NCBI]
3.77733e-05
PWS
[NCBI]
3.62079e-05
SMS
[NCBI]
3.53857e-05
RTT
[NCBI]
2.23204e-05
HD
[NCBI]
2.08325e-05
BWS
[NCBI]
1.90532e-05
NGFB
[NCBI]
9.48694e-06
apnea, obstructive sleep
[NCBI]
1.65575e-06
Database Center for Life Science