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MeSH keywords -> Related genes, diseases (OMIM)


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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