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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hearing Disorders [NCBI]


Gene


Gene Link Information
Gain
01
AUTS3 [NCBI] 0.000345139
DFNA18 [NCBI] 0.000284409
ADFN [NCBI] 0.000261497
GJB2 [NCBI] 0.000154032
HFM [NCBI] 0.000137693
TRNL1 [NCBI] 0.000133816
MS [NCBI] 0.000121158
GJB3 [NCBI] 2.77895e-05
MYO7A [NCBI] 2.48138e-05
SLC26A5 [NCBI] 2.37663e-05
UBR1 [NCBI] 2.25002e-05
PAX3 [NCBI] 2.10224e-05
DIAPH1 [NCBI] 1.98646e-05
TECTA [NCBI] 1.95153e-05
COCH [NCBI] 1.75491e-05
WFS1 [NCBI] 1.71386e-05
EFHA1 [NCBI] 1.61663e-05
GJB6 [NCBI] 1.59785e-05
CHRNA10 [NCBI] 1.3786e-05
OTOA [NCBI] 1.3786e-05
SLC44A2 [NCBI] 1.28876e-05
EML1 [NCBI] 1.28876e-05
DFNB59 [NCBI] 1.23043e-05
OTOG [NCBI] 1.23043e-05
MAB21L1 [NCBI] 1.18705e-05
MCOLN3 [NCBI] 1.09915e-05
CLRN1 [NCBI] 9.44157e-06
LRP2 [NCBI] 9.26553e-06
TRPA1 [NCBI] 8.89139e-06
TMPRSS3 [NCBI] 8.89139e-06
CPE [NCBI] 8.27703e-06
USH1C [NCBI] 8.1857e-06
EYA1 [NCBI] 7.3299e-06
SLC26A4 [NCBI] 7.22555e-06
KCNE1 [NCBI] 7.03433e-06
GAA [NCBI] 6.54665e-06
RPGR [NCBI] 6.32464e-06
MPZ [NCBI] 6.32464e-06
ERCC5 [NCBI] 5.90589e-06
NLRP3 [NCBI] 5.8715e-06
COL2A1 [NCBI] 5.7939e-06
MITF [NCBI] 5.34948e-06
XPC [NCBI] 5.31661e-06
XPA [NCBI] 5.30042e-06
KIT [NCBI] 5.05382e-06
KCNQ1 [NCBI] 4.7161e-06
PAX6 [NCBI] 4.69923e-06
TGFBR1 [NCBI] 4.31263e-06
GJB1 [NCBI] 4.21842e-06
NAT2 [NCBI] 3.89219e-06
SLC6A4 [NCBI] 3.3791e-06
VHL [NCBI] 3.28443e-06
GSTT1 [NCBI] 3.23476e-06
GSTM1 [NCBI] 2.93191e-06
SOD1 [NCBI] 2.55056e-06
BDNF [NCBI] 2.44307e-06
ACHE [NCBI] 2.33724e-06
EPO [NCBI] 1.47626e-06
NGF [NCBI] 1.47323e-06




OMIM


OMIM Link Information
gain
01
DFN2 [NCBI] 0.0018571
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000971879
mohr syndrome [NCBI] 0.000971879
otodental dysplasia [NCBI] 0.000714117
DFNA18 [NCBI] 0.000714117
atresia of external auditory canal and conduction deafness [NCBI] 0.000714117
mental retardation with optic atrophy, deafness, and seizures [NCBI] 0.000632262
HCFP2 [NCBI] 0.000632262
deafness, high-frequency sensorineural, x-linked [NCBI] 0.000632262
autism, susceptibility to, 3 [NCBI] 0.000579249
IOSCA [NCBI] 0.000508689
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.000441356
acrodysostosis [NCBI] 0.000441356
dupuytren contracture [NCBI] 0.000424262
ADFN [NCBI] 0.000408926
OSCS [NCBI] 0.000370626
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000370626
USH2A [NCBI] 0.000352915
BOR1 [NCBI] 0.000327329
usher syndrome, type i [NCBI] 0.000317071
BOS1 [NCBI] 0.000295371
dubowitz syndrome [NCBI] 0.000287577
alport syndrome, autosomal dominant [NCBI] 0.000199022
RA [NCBI] 0.000175942
knuckle pads, leukonychia, and sensorineural deafness [NCBI] 0.000165683
GJB2 [NCBI] 0.000143219
deafness, aminoglycoside-induced [NCBI] 0.000143023
WS1 [NCBI] 0.000137641
DFNA6 [NCBI] 0.000132713
LADD [NCBI] 0.000129903
USH1C [NCBI] 0.000129903
klippel-trenaunay-weber syndrome [NCBI] 0.000127275
marshall syndrome [NCBI] 0.000122709
TUB [NCBI] 0.000119275
HFM [NCBI] 0.000119138
SLE [NCBI] 0.000115121
thumb, hypoplastic, with choroid coloboma, poorly developed antihelix, and deafness [NCBI] 0.000110008
deafness, progressive, with stapes fixation [NCBI] 0.000110008
DFNB22 [NCBI] 0.000110008
epiphyseal dysplasia of femoral head, myopia, and deafness [NCBI] 0.000110008
ectodermal dysplasia and neurosensory deafness [NCBI] 0.000110008
deafness, neural, congenital moderate [NCBI] 0.000110008
ATS [NCBI] 8.97934e-05
WFS1 [NCBI] 8.76103e-05
vestibulocochlear dysfunction, progressive [NCBI] 8.75539e-05
deafness-oligodontia syndrome [NCBI] 8.75539e-05
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia [NCBI] 8.75539e-05
aniridia, partial, with unilateral renal agenesis and psychomotor retardation [NCBI] 8.75539e-05
growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction [NCBI] 8.75539e-05
ophthalmoplegic neuromuscular disorder with abnormal mitochondria [NCBI] 8.75539e-05
PDS [NCBI] 8.18609e-05
ataxia-deafness-retardation syndrome [NCBI] 7.909e-05
otofaciocervical syndrome [NCBI] 7.909e-05
NF2 [NCBI] 7.70251e-05
PAX3 [NCBI] 7.66285e-05
coloboma of macula with type b brachydactyly [NCBI] 7.35999e-05
charge-like syndrome, x-linked [NCBI] 7.35999e-05
DFNB59 [NCBI] 7.35999e-05
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities [NCBI] 7.35999e-05
CF [NCBI] 7.20758e-05
MTTL1 [NCBI] 7.09593e-05
retinitis pigmentosa, x-linked, with recurrent respiratory infections [NCBI] 6.95222e-05
OTOA [NCBI] 6.80811e-05
TECTB [NCBI] 6.80811e-05
DFNA1 [NCBI] 6.35801e-05
monosomy 1p36 syndrome [NCBI] 6.35801e-05
keutel syndrome [NCBI] 6.35801e-05
OTOG [NCBI] 6.28823e-05
MTTV [NCBI] 6.28823e-05
pejvakin [NCBI] 5.9507e-05
DFNB9 [NCBI] 5.74745e-05
BDB1 [NCBI] 5.74745e-05
deafness, autosomal recessive [NCBI] 5.74745e-05
DFNA12 [NCBI] 5.5869e-05
sturge-weber syndrome [NCBI] 5.5869e-05
RP [NCBI] 5.52615e-05
VHL [NCBI] 5.52149e-05
USH3 [NCBI] 5.30772e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 5.30772e-05
PBT [NCBI] 5.30772e-05
indifference to pain, congenital, autosomal recessive [NCBI] 5.18473e-05
SFD [NCBI] 5.07066e-05
KSS [NCBI] 5.00769e-05
MTS [NCBI] 4.96433e-05
MCOPS3 [NCBI] 4.86477e-05
diabetes-deafness syndrome, maternally transmitted [NCBI] 4.86477e-05
TECTA [NCBI] 4.68449e-05
COL11A1 [NCBI] 4.60821e-05
RHS [NCBI] 4.5201e-05
CMDD [NCBI] 4.5201e-05
KL [NCBI] 4.40943e-05
USH1C [NCBI] 4.35119e-05
JBS [NCBI] 4.30413e-05
GLDC [NCBI] 4.29619e-05
EYA1 [NCBI] 4.19464e-05
WFS1 [NCBI] 4.10261e-05
GJB3 [NCBI] 4.05964e-05
OMP [NCBI] 4.05964e-05
DFNB1 [NCBI] 4.05659e-05
OFD1 [NCBI] 4.05659e-05
RIEG1 [NCBI] 4.05659e-05
leopard syndrome 1 [NCBI] 3.89419e-05
DYX1 [NCBI] 3.89419e-05
EKV [NCBI] 3.84372e-05
CPE [NCBI] 3.80225e-05
COL4A5 [NCBI] 3.77044e-05
mucopolysaccharidosis type vi [NCBI] 3.74756e-05
MTTK [NCBI] 3.73963e-05
AQP4 [NCBI] 3.70976e-05
EVA [NCBI] 3.6572e-05
FCAS [NCBI] 3.6572e-05
SLC26A4 [NCBI] 3.59867e-05
KIT [NCBI] 3.59867e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 3.47554e-05
KCNQ1 [NCBI] 3.28694e-05
mucopolysaccharidosis type iva [NCBI] 3.26808e-05
RPGR [NCBI] 3.21362e-05
UCN [NCBI] 3.14548e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 3.1132e-05
ABCD1 [NCBI] 3.06657e-05
ND [NCBI] 2.67383e-05
osteogenesis imperfecta, type i [NCBI] 2.34071e-05
ALD [NCBI] 2.16827e-05
MAS [NCBI] 1.83108e-05
PCD [NCBI] 1.36741e-05
AD [NCBI] 1.17739e-05
WBS [NCBI] 1.16435e-05
GDNF [NCBI] 1.11638e-05
BDNF [NCBI] 4.92304e-06
ACHE [NCBI] 4.10887e-06
temporal arteritis [NCBI] 2.72772e-06
MDD [NCBI] 1.50645e-06
EPO [NCBI] 1.0743e-06
NGFB [NCBI] 1.00901e-06
PWS [NCBI] 4.94127e-07




Database Center for Life Science