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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hearing Loss, Bilateral [NCBI]

Gene


 Gene Link Information
Gain		 01
DFNA49 [NCBI] 0.000381162
SCAX3 [NCBI] 0.000381162
DFNB15 [NCBI] 0.000320423
DFNB63 [NCBI] 0.000297502
TRNS1 [NCBI] 0.000234392
RNR1 [NCBI] 0.000185014
GJB2 [NCBI] 0.000116054
TECTA [NCBI] 2.28153e-05
HOXA2 [NCBI] 1.45183e-05
LHFPL5 [NCBI] 1.3501e-05
ATP2B2 [NCBI] 1.16119e-05
SIX1 [NCBI] 1.05201e-05
TCOF1 [NCBI] 9.5268e-06
GJB3 [NCBI] 8.95536e-06
KCNE1 [NCBI] 8.65876e-06
RPS19 [NCBI] 8.65876e-06
GJA1 [NCBI] 8.20334e-06
GATA3 [NCBI] 7.81627e-06
KCNQ1 [NCBI] 6.32155e-06
SLC5A5 [NCBI] 6.06645e-06
FGFR3 [NCBI] 5.47439e-06
TNFRSF11A [NCBI] 4.97064e-06
VHL [NCBI] 4.85475e-06
TNFSF11 [NCBI] 4.7354e-06



OMIM


 OMIM Link Information
gain		 01
CMDR [NCBI] 0.00160037
DFNA49 [NCBI] 0.00111789
DFNB63 [NCBI] 0.00111789
otodental dysplasia [NCBI] 0.000900049
alport syndrome, autosomal dominant [NCBI] 0.000372668
kabuki syndrome [NCBI] 0.00034134
FSHMD1A [NCBI] 0.000255317
GJB2 [NCBI] 0.000191374
OPD2 [NCBI] 0.000157392
FMD [NCBI] 0.00015543
usher syndrome, type i [NCBI] 0.000132105
SEDC [NCBI] 0.000131197
atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease [NCBI] 0.000128309
hypospadias, hypertelorism, upper lid coloboma, and mixed-type hearing loss [NCBI] 0.000128309
optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant [NCBI] 0.000128309
DFNA23 [NCBI] 0.000105843
spinocerebellar ataxia, x-linked 3 [NCBI] 0.000105843
camptodactyly, tall stature, and hearing loss syndrome [NCBI] 0.000105843
hydrocephalus with cerebellar agenesis [NCBI] 9.73662e-05
DFNB67 [NCBI] 9.73662e-05
ivic syndrome [NCBI] 9.18637e-05
DFNA1 [NCBI] 8.18067e-05
muenke syndrome [NCBI] 7.56639e-05
LHFPL5 [NCBI] 7.40637e-05
DFNA12 [NCBI] 7.4046e-05
alport syndrome, autosomal recessive [NCBI] 7.25761e-05
USH1C [NCBI] 7.12295e-05
LADD [NCBI] 7.12295e-05
OPD1 [NCBI] 6.88341e-05
BOS1 [NCBI] 6.77584e-05
LRS1 [NCBI] 6.77584e-05
heterotopia, periventricular, x-linked dominant [NCBI] 6.67504e-05
diabetes-deafness syndrome, maternally transmitted [NCBI] 6.67504e-05
JLNS1 [NCBI] 6.40591e-05
SIX1 [NCBI] 6.30871e-05
deafness, conductive, with stapes fixation [NCBI] 6.17564e-05
MNS [NCBI] 6.17564e-05
JBS [NCBI] 6.10572e-05
DFNB1 [NCBI] 5.85321e-05
BOR1 [NCBI] 5.63538e-05
HCH [NCBI] 5.48965e-05
MTTS1 [NCBI] 5.46665e-05
MTCYB [NCBI] 5.35922e-05
GJB3 [NCBI] 5.17404e-05
PDS [NCBI] 4.76007e-05
FLNA [NCBI] 4.73736e-05
AMC [NCBI] 4.3976e-05
KCNQ1 [NCBI] 4.39635e-05
TD1 [NCBI] 4.18254e-05
COL2A1 [NCBI] 4.00503e-05
WHS [NCBI] 3.95894e-05
INSR [NCBI] 3.6879e-05
ACH [NCBI] 3.51233e-05
DBA [NCBI] 3.49952e-05
FGFR3 [NCBI] 2.92978e-05
SLE [NCBI] 1.07539e-05
CF [NCBI] 8.59445e-06



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