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01 Hearing Loss [NCBI]

Gene


 Gene Link Information
Gain		 01
RNR1 [NCBI] 0.00209101
TRNS1 [NCBI] 0.00114187
RNR1 [NCBI] 0.000842411
GJB2 [NCBI] 0.000827072
DFNB63 [NCBI] 0.000502541
TRNL1 [NCBI] 0.000394281
DFNB47 [NCBI] 0.000292547
DFNA47 [NCBI] 0.000292547
AUNA1 [NCBI] 0.000292547
DFNB44 [NCBI] 0.000292547
DFNB45 [NCBI] 0.000292547
DFNB68 [NCBI] 0.000292547
DFNB65 [NCBI] 0.000292547
SCAX3 [NCBI] 0.000292547
DFNB55 [NCBI] 0.000292547
DFNA53 [NCBI] 0.000292547
DFNA54 [NCBI] 0.000292547
DFNY1 [NCBI] 0.000292547
DFNA41 [NCBI] 0.000231856
OTSC5 [NCBI] 0.000231856
DFNB33 [NCBI] 0.000231856
DFNB15 [NCBI] 0.000231856
DFNA21 [NCBI] 0.000208982
GJB6 [NCBI] 0.000199319
TRNK [NCBI] 0.000160852
MS [NCBI] 0.000123832
HFM [NCBI] 8.67248e-05
COCH [NCBI] 7.23543e-05
MYO7A [NCBI] 6.22049e-05
EYA1 [NCBI] 5.98629e-05
SLC26A4 [NCBI] 5.90945e-05
TMC1 [NCBI] 5.21242e-05
DFNA5 [NCBI] 3.6964e-05
ESPN [NCBI] 3.20267e-05
USH2A [NCBI] 3.17753e-05
SLC26A2 [NCBI] 3.06211e-05
WFS1 [NCBI] 3.02761e-05
GJB3 [NCBI] 3.01649e-05
POU4F3 [NCBI] 2.93754e-05
EYA4 [NCBI] 2.86086e-05
TMPRSS3 [NCBI] 2.59055e-05
OTOF [NCBI] 2.53113e-05
PCDH15 [NCBI] 2.53113e-05
MYO6 [NCBI] 2.53113e-05
TECTA [NCBI] 2.4779e-05
KCNQ4 [NCBI] 2.46132e-05
CDH23 [NCBI] 2.44525e-05
COL2A1 [NCBI] 2.39169e-05
MARVELD2 [NCBI] 2.21234e-05
LHFPL5 [NCBI] 2.21234e-05
KIAA1199 [NCBI] 2.07114e-05
TMIE [NCBI] 2.01783e-05
MYH9 [NCBI] 1.94354e-05
SLC26A5 [NCBI] 1.93115e-05
COL4A5 [NCBI] 1.87722e-05
MYH14 [NCBI] 1.83219e-05
COX1 [NCBI] 1.8047e-05
ATOH1 [NCBI] 1.73342e-05
BMP4 [NCBI] 1.45693e-05
CISD2 [NCBI] 1.39467e-05
TMC4 [NCBI] 1.39467e-05
SLC26A11 [NCBI] 1.39467e-05
TMC3 [NCBI] 1.39467e-05
TMC7 [NCBI] 1.39467e-05
ZFAND5 [NCBI] 1.15667e-05
EFR3A [NCBI] 1.15667e-05
TMC5 [NCBI] 1.15667e-05
OPA1 [NCBI] 1.12191e-05
COL11A2 [NCBI] 1.11149e-05
OTOS [NCBI] 1.06687e-05
CCDC50 [NCBI] 1.06687e-05
SLC44A2 [NCBI] 1.06687e-05
YAF2 [NCBI] 1.06687e-05
CLDN14 [NCBI] 1.00857e-05
TRIOBP [NCBI] 1.00857e-05
TMC2 [NCBI] 1.00857e-05
NOG [NCBI] 9.87431e-06
FAM3C [NCBI] 9.65232e-06
KCNK6 [NCBI] 9.65232e-06
BARX1 [NCBI] 9.30707e-06
GJD2 [NCBI] 9.30707e-06
KCNQ5 [NCBI] 9.02004e-06
FOXI1 [NCBI] 9.02004e-06
ND6 [NCBI] 8.7744e-06
RDX [NCBI] 8.5597e-06
COL1A1 [NCBI] 8.37403e-06
PRPS1 [NCBI] 8.36902e-06
ESRRB [NCBI] 8.36902e-06
OGN [NCBI] 8.19752e-06
CHML [NCBI] 8.19752e-06
TMC8 [NCBI] 7.89896e-06
HRK [NCBI] 7.76724e-06
GPR98 [NCBI] 7.64499e-06
TMC6 [NCBI] 7.53094e-06
ND4 [NCBI] 7.53094e-06
MYO15A [NCBI] 7.42406e-06
CLRN1 [NCBI] 7.22856e-06
POU3F4 [NCBI] 7.13865e-06
KIF21A [NCBI] 7.05326e-06
SALL4 [NCBI] 6.82022e-06
SIX1 [NCBI] 6.68097e-06
TRPA1 [NCBI] 6.68097e-06
SACS [NCBI] 6.61542e-06
ALMS1 [NCBI] 6.55231e-06
SOST [NCBI] 6.55231e-06
DUOX2 [NCBI] 6.55231e-06
DIAPH1 [NCBI] 6.49148e-06
CA2 [NCBI] 6.07067e-06
C10orf2 [NCBI] 6.07067e-06
PITX2 [NCBI] 6.07067e-06
USH1C [NCBI] 5.98008e-06
MCOLN1 [NCBI] 5.85276e-06
KEAP1 [NCBI] 5.81238e-06
MTAP [NCBI] 5.73443e-06
SBDS [NCBI] 5.73443e-06
FLNA [NCBI] 5.65995e-06
OAT [NCBI] 5.39141e-06
SNAP25 [NCBI] 5.0813e-06
SOX2 [NCBI] 5.03067e-06
DIO2 [NCBI] 4.98155e-06
CHM [NCBI] 4.98155e-06
FOXC1 [NCBI] 4.91051e-06
IDS [NCBI] 4.63391e-06
NF2 [NCBI] 4.63391e-06
COL1A2 [NCBI] 4.50234e-06
TNFRSF11B [NCBI] 4.38683e-06
POLG [NCBI] 4.29899e-06
MPZ [NCBI] 4.14715e-06
NLRP3 [NCBI] 3.70696e-06
TJP1 [NCBI] 2.75032e-06
FGF23 [NCBI] 2.72715e-06
ERBB4 [NCBI] 2.52387e-06
GDNF [NCBI] 2.44627e-06
IL1RN [NCBI] 2.37991e-06
GJB1 [NCBI] 2.14641e-06
TPO [NCBI] 2.13886e-06
PMP22 [NCBI] 2.07631e-06
FGFR3 [NCBI] 1.84637e-06
BMP2 [NCBI] 1.65207e-06
TNFRSF11A [NCBI] 1.42017e-06
VHL [NCBI] 1.32573e-06
GSTT1 [NCBI] 1.28421e-06
IL1B [NCBI] 1.20922e-06
GSTM1 [NCBI] 1.03728e-06
GSTP1 [NCBI] 9.92144e-07
TNF [NCBI] 9.8732e-07
SOD1 [NCBI] 7.44836e-07
BDNF [NCBI] 6.66986e-07
CAT [NCBI] 6.63304e-07
HGF [NCBI] 3.46877e-07
GER [NCBI] 3.19324e-07
EGF [NCBI] 2.88688e-07
TGFB1 [NCBI] 1.75131e-07
TP53 [NCBI] 7.35498e-08



OMIM


 OMIM Link Information
gain		 01
microtia with meatal atresia and conductive deafness [NCBI] 0.00109814
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.00109814
DFNA47 [NCBI] 0.000919326
DFNB68 [NCBI] 0.000919326
DFNA53 [NCBI] 0.000919326
DFNB55 [NCBI] 0.000919326
deafness, neurosensory, autosomal recessive 47 [NCBI] 0.000919326
DFNB44 [NCBI] 0.000919326
DFNB32 [NCBI] 0.000919326
GJB2 [NCBI] 0.000772236
otodental dysplasia [NCBI] 0.000701812
DFNA41 [NCBI] 0.000701812
atresia of external auditory canal and conduction deafness [NCBI] 0.000701812
earlobes, thickened, with conductive deafness from incudostapedial abnormalities [NCBI] 0.000619991
auditory neuropathy, autosomal dominant, 1 [NCBI] 0.000619991
vitreoretinal degeneration, snowflake type [NCBI] 0.000619991
DFNB15 [NCBI] 0.000567013
vestibulopathy, familial [NCBI] 0.000496521
PCA [NCBI] 0.000412232
BOR1 [NCBI] 0.000404125
OTSC1 [NCBI] 0.00039693
FSHMD1A [NCBI] 0.000356772
varadi-papp syndrome [NCBI] 0.000347941
MAFD1 [NCBI] 0.000224755
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies [NCBI] 0.000217385
RA [NCBI] 0.000198189
GJB6 [NCBI] 0.000193412
osteogenesis imperfecta, type i [NCBI] 0.000175461
ivic syndrome [NCBI] 0.000172479
DFNA5 [NCBI] 0.000162528
kabuki syndrome [NCBI] 0.000160115
EVA [NCBI] 0.000159553
RP [NCBI] 0.000143862
deafness, aminoglycoside-induced [NCBI] 0.000140241
SLE [NCBI] 0.000131039
WFS1 [NCBI] 0.000131031
SYNS1 [NCBI] 0.000127127
BOS1 [NCBI] 0.000119937
MTRNR1 [NCBI] 0.000118764
MYO7A [NCBI] 0.000117866
HFM [NCBI] 0.000109525
DFNB24 [NCBI] 0.000108618
optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant [NCBI] 0.000108618
ossicular malformations, familial [NCBI] 0.000108618
deafness, conductive stapedial, with ear malformation and facial palsy [NCBI] 0.000108618
USH2A [NCBI] 0.000106223
TMC1 [NCBI] 0.000104585
DFNB1 [NCBI] 0.0001011
pfeiffer syndrome [NCBI] 9.56883e-05
COL2A1 [NCBI] 9.38869e-05
usher syndrome, type i [NCBI] 9.28412e-05
TBS [NCBI] 9.19473e-05
charge syndrome [NCBI] 9.10785e-05
OTOF [NCBI] 8.63465e-05
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia [NCBI] 8.61652e-05
WFS2 [NCBI] 8.61652e-05
spinocerebellar ataxia, x-linked 3 [NCBI] 8.61652e-05
DFNB49 [NCBI] 8.61652e-05
DFNB28 [NCBI] 8.61652e-05
DHS [NCBI] 8.61652e-05
ichthyosis, hystrix-like, with deafness [NCBI] 8.61652e-05
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia [NCBI] 8.61652e-05
DFNA44 [NCBI] 8.61652e-05
epiphyseal dysplasia, multiple, with myopia and conductive deafness [NCBI] 8.61652e-05
USH2A [NCBI] 8.50679e-05
CDH23 [NCBI] 8.16664e-05
EYA1 [NCBI] 8.0652e-05
NOG [NCBI] 8.0652e-05
PDS [NCBI] 7.91538e-05
hydrocephalus with cerebellar agenesis [NCBI] 7.77029e-05
DFNB67 [NCBI] 7.77029e-05
ARTS [NCBI] 7.77029e-05
otofaciocervical syndrome [NCBI] 7.77029e-05
PCDH9 [NCBI] 7.30386e-05
SLC26A11 [NCBI] 7.30386e-05
ZFAND5 [NCBI] 7.30386e-05
MARVELD2 [NCBI] 7.30386e-05
KCNRG [NCBI] 7.30386e-05
SLC26A5 [NCBI] 7.30386e-05
CISD2 [NCBI] 7.30386e-05
otospiralin [NCBI] 7.30386e-05
stapes ankylosis with broad thumb and toes [NCBI] 7.22145e-05
charge-like syndrome, x-linked [NCBI] 7.22145e-05
carbimazole sensitivity [NCBI] 7.22145e-05
branchial arch syndrome, x-linked [NCBI] 7.22145e-05
BMP4 [NCBI] 7.20034e-05
SLC26A4 [NCBI] 6.85226e-05
DFNB6 [NCBI] 6.81384e-05
stickler syndrome, type i, nonsyndromic ocular [NCBI] 6.48942e-05
DFNA11 [NCBI] 6.48942e-05
zunich neuroectodermal syndrome [NCBI] 6.48942e-05
USH2C [NCBI] 6.48942e-05
DFNA1 [NCBI] 6.21996e-05
kiaa1199 [NCBI] 5.92642e-05
CCDC50 [NCBI] 5.92642e-05
PCDH8 [NCBI] 5.92642e-05
EFR3A [NCBI] 5.92642e-05
TRIOBP [NCBI] 5.92642e-05
TMIE [NCBI] 5.92642e-05
DFNA9 [NCBI] 5.60989e-05
DFNB9 [NCBI] 5.60989e-05
fabry disease [NCBI] 5.50697e-05
spinocerebellar ataxia, 16q22-linked [NCBI] 5.4495e-05
OSMED [NCBI] 5.4495e-05
DFNA12 [NCBI] 5.4495e-05
LHFPL5 [NCBI] 5.40692e-05
RDX [NCBI] 5.40692e-05
CDKN2D [NCBI] 5.40692e-05
CF [NCBI] 5.3355e-05
DFNA6 [NCBI] 5.30392e-05
wildervanck syndrome [NCBI] 5.30392e-05
HRK [NCBI] 5.06977e-05
FOXI1 [NCBI] 5.06977e-05
CHML [NCBI] 5.06977e-05
ESPN [NCBI] 5.06977e-05
SYM1 [NCBI] 5.04782e-05
SACS [NCBI] 5.04782e-05
MCOPS2 [NCBI] 5.04782e-05
multiple pterygium syndrome, escobar variant [NCBI] 4.93392e-05
WGN1 [NCBI] 4.93392e-05
LRS1 [NCBI] 4.82776e-05
mannosidosis, beta a, lysosomal [NCBI] 4.82776e-05
muckle-wells syndrome [NCBI] 4.82776e-05
DIO2 [NCBI] 4.81923e-05
OPD2 [NCBI] 4.72836e-05
diabetes-deafness syndrome, maternally transmitted [NCBI] 4.72836e-05
CYLD [NCBI] 4.63494e-05
GPR98 [NCBI] 4.61971e-05
SOST [NCBI] 4.46345e-05
CLDN14 [NCBI] 4.45389e-05
CMDD [NCBI] 4.38435e-05
HEPOD [NCBI] 4.38435e-05
PRPS1 [NCBI] 4.31203e-05
deafness, conductive, with stapes fixation [NCBI] 4.23739e-05
TRPS1 [NCBI] 4.23739e-05
SACS [NCBI] 4.18808e-05
JBS [NCBI] 4.16888e-05
refsum disease [NCBI] 4.1033e-05
EYA4 [NCBI] 4.07804e-05
KAL2 [NCBI] 3.98005e-05
MELAS [NCBI] 3.98005e-05
MHA [NCBI] 3.92198e-05
GATA3 [NCBI] 3.88925e-05
TECTA [NCBI] 3.80695e-05
COCH [NCBI] 3.73104e-05
PKS [NCBI] 3.66109e-05
PCDH15 [NCBI] 3.66062e-05
DA2A [NCBI] 3.56825e-05
SEDC [NCBI] 3.48087e-05
MTTS1 [NCBI] 3.47553e-05
USH1C [NCBI] 3.47553e-05
STL1 [NCBI] 3.39836e-05
MYH9 [NCBI] 3.32012e-05
MTND5 [NCBI] 3.32012e-05
OPA1 [NCBI] 3.2734e-05
WFS1 [NCBI] 3.14146e-05
DM2 [NCBI] 2.92339e-05
COL4A5 [NCBI] 2.90006e-05
GLA [NCBI] 2.78376e-05
MTAP [NCBI] 2.56487e-05
NF2 [NCBI] 2.35229e-05
CCD [NCBI] 2.21547e-05
MPZ [NCBI] 1.90947e-05
COL1A1 [NCBI] 1.80002e-05
BBS [NCBI] 1.63414e-05
VHL [NCBI] 1.62347e-05
KSS [NCBI] 1.39364e-05
PMP22 [NCBI] 1.32565e-05
PCD [NCBI] 1.25614e-05
FGFR3 [NCBI] 1.05586e-05
CPI [NCBI] 1.03347e-05
TPO [NCBI] 8.4302e-06
XDH [NCBI] 5.93297e-06
BWS [NCBI] 5.42963e-06
GDNF [NCBI] 4.29143e-06
TNFRSF11B [NCBI] 3.17181e-06
temporal arteritis [NCBI] 2.10092e-06
EGF [NCBI] 1.20322e-06
BDNF [NCBI] 4.15977e-07
CAT [NCBI] 3.97874e-07
PD [NCBI] 1.83855e-08
HGF [NCBI] 6.09316e-10



Database Center for Life Science