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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hearing Loss, Sensorineural [NCBI]

Gene


 Gene Link Information
Gain		 01
RNR1 [NCBI] 0.00207988
GJB2 [NCBI] 0.00145291
RNR1 [NCBI] 0.000747107
AUNX1 [NCBI] 0.000539277
DFNB17 [NCBI] 0.000539277
USH2B [NCBI] 0.000539277
DFNA21 [NCBI] 0.000455695
SLC26A4 [NCBI] 0.000418302
MYO7A [NCBI] 0.000337306
HFM [NCBI] 0.000336712
TRNL1 [NCBI] 0.000324973
TRNS1 [NCBI] 0.000311565
COCH [NCBI] 0.000293582
MCDR4 [NCBI] 0.000269326
DFNA52 [NCBI] 0.000269326
DFNA7 [NCBI] 0.000269326
NEDE [NCBI] 0.000269326
DFNA31 [NCBI] 0.000269326
DFNB27 [NCBI] 0.000269326
MRPS18CP2 [NCBI] 0.000269326
DFN8 [NCBI] 0.000269326
TRNAL2 [NCBI] 0.000269326
DFNA50 [NCBI] 0.000269326
DFNB14 [NCBI] 0.000269326
MPDMRS [NCBI] 0.000269326
DFNA43 [NCBI] 0.000269326
DFNA16 [NCBI] 0.000269326
DFNA30 [NCBI] 0.000269326
DFN4 [NCBI] 0.000269326
DFNA27 [NCBI] 0.000269326
EKV3 [NCBI] 0.000269326
DFNB62 [NCBI] 0.000269326
DFNA49 [NCBI] 0.000269326
DFNB40 [NCBI] 0.000269326
DFNB39 [NCBI] 0.000269326
DFNB20 [NCBI] 0.000269326
DFNA42 [NCBI] 0.000269326
USH1E [NCBI] 0.000208673
DFNA24 [NCBI] 0.000208673
CATSPER2P1 [NCBI] 0.000208673
DFN2 [NCBI] 0.000208673
DFNM2 [NCBI] 0.000208673
GJB6 [NCBI] 0.000198704
DFNB63 [NCBI] 0.000185838
KCNQ4 [NCBI] 0.000171597
USH2A [NCBI] 0.000166439
CDH23 [NCBI] 0.000145944
MS [NCBI] 0.000141007
OTOF [NCBI] 0.000139096
TECTA [NCBI] 0.00013593
CACD [NCBI] 0.000123422
CLRN1 [NCBI] 0.000101361
MYH9 [NCBI] 8.86429e-05
SALL1 [NCBI] 8.68785e-05
ATP6V1B1 [NCBI] 8.27033e-05
POU4F3 [NCBI] 8.27033e-05
WFS1 [NCBI] 7.66498e-05
GJB3 [NCBI] 6.69542e-05
DFNA5 [NCBI] 6.12819e-05
ALMS1 [NCBI] 5.97032e-05
EYA4 [NCBI] 5.61545e-05
BSND [NCBI] 5.11659e-05
USH1C [NCBI] 4.56081e-05
POU3F4 [NCBI] 4.26313e-05
PCDH15 [NCBI] 3.90634e-05
BCS1L [NCBI] 3.64284e-05
USH1G [NCBI] 3.64284e-05
COL11A2 [NCBI] 3.54624e-05
TMC1 [NCBI] 3.36239e-05
DFNB59 [NCBI] 3.32854e-05
GATA3 [NCBI] 3.32143e-05
ACTG1 [NCBI] 3.27621e-05
NDP [NCBI] 3.09516e-05
TIMM8A [NCBI] 2.9846e-05
DIAPH1 [NCBI] 2.95875e-05
SLC19A2 [NCBI] 2.90691e-05
ATP6V0A4 [NCBI] 2.80648e-05
CLCNKB [NCBI] 2.58012e-05
TECTB [NCBI] 2.47617e-05
NLRP3 [NCBI] 2.44645e-05
COL2A1 [NCBI] 2.40752e-05
MITF [NCBI] 2.1854e-05
OPA1 [NCBI] 2.10266e-05
FGFR3 [NCBI] 1.93476e-05
STRC [NCBI] 1.82087e-05
DFNB31 [NCBI] 1.82087e-05
TBL1X [NCBI] 1.65842e-05
SLC26A5 [NCBI] 1.6179e-05
TCF21 [NCBI] 1.6179e-05
PMP22 [NCBI] 1.5891e-05
COL11A1 [NCBI] 1.49175e-05
ATP2B2 [NCBI] 1.49175e-05
MYO15A [NCBI] 1.42071e-05
COL4A5 [NCBI] 1.41319e-05
CLCNKA [NCBI] 1.362e-05
PTPRJ [NCBI] 1.29684e-05
TMPRSS3 [NCBI] 1.26844e-05
SLC4A5 [NCBI] 1.23794e-05
GRHL1 [NCBI] 1.23794e-05
LBX2 [NCBI] 1.23794e-05
BDNF [NCBI] 1.09645e-05
CATSPER2 [NCBI] 1.00002e-05
NUPL2 [NCBI] 1.00002e-05
HISPPD2A [NCBI] 1.00002e-05
CKMT1A [NCBI] 9.10297e-06
TMEM2 [NCBI] 9.10297e-06
CLDN23 [NCBI] 9.10297e-06
EML1 [NCBI] 9.10297e-06
SARS [NCBI] 9.10297e-06
SLC17A8 [NCBI] 9.10297e-06
CCDC50 [NCBI] 9.10297e-06
MMP23B [NCBI] 9.10297e-06
NUCB2 [NCBI] 9.10297e-06
P2RY14 [NCBI] 8.52075e-06
LHFPL5 [NCBI] 8.08814e-06
PFN2 [NCBI] 8.08814e-06
TBL1Y [NCBI] 8.08814e-06
GRHL2 [NCBI] 8.08814e-06
MCM10 [NCBI] 8.08814e-06
LHX3 [NCBI] 7.74365e-06
MTO1 [NCBI] 7.74365e-06
GNB1L [NCBI] 7.74365e-06
RPGR [NCBI] 7.58539e-06
GSC [NCBI] 7.45738e-06
KIAA1199 [NCBI] 7.45738e-06
TMIE [NCBI] 7.2125e-06
FOXN3 [NCBI] 7.2125e-06
MYO1A [NCBI] 7.2125e-06
CRMP1 [NCBI] 6.80864e-06
COL9A1 [NCBI] 6.80864e-06
PRPS1 [NCBI] 6.80864e-06
SIAH2 [NCBI] 6.80864e-06
SLC26A6 [NCBI] 6.63791e-06
TWIST1 [NCBI] 6.56141e-06
VPS33B [NCBI] 6.48285e-06
MYH14 [NCBI] 6.34086e-06
SEPT5 [NCBI] 6.20991e-06
GPR98 [NCBI] 6.08842e-06
PICALM [NCBI] 6.08842e-06
F2 [NCBI] 6.0557e-06
EVC [NCBI] 5.97513e-06
SLC4A11 [NCBI] 5.97513e-06
ATOH1 [NCBI] 5.869e-06
DEFA3 [NCBI] 5.67503e-06
DCTN1 [NCBI] 5.67503e-06
ATP6 [NCBI] 5.58588e-06
PEX6 [NCBI] 5.50125e-06
LRP2 [NCBI] 5.50125e-06
ND5 [NCBI] 5.42072e-06
TFCP2 [NCBI] 5.34391e-06
COL9A3 [NCBI] 5.2705e-06
PAX3 [NCBI] 5.26779e-06
PRCD [NCBI] 5.2002e-06
F5 [NCBI] 5.12619e-06
LAMB1 [NCBI] 5.00563e-06
NCOR2 [NCBI] 4.94556e-06
MYO6 [NCBI] 4.94556e-06
NCOR1 [NCBI] 4.8876e-06
FOXE1 [NCBI] 4.8876e-06
SLC16A2 [NCBI] 4.83162e-06
PFN1 [NCBI] 4.83162e-06
HDAC3 [NCBI] 4.62507e-06
SIX3 [NCBI] 4.62507e-06
KCNQ1 [NCBI] 4.53921e-06
ACTB [NCBI] 4.53084e-06
ALS2 [NCBI] 4.48569e-06
KCNQ3 [NCBI] 4.44177e-06
MERTK [NCBI] 4.399e-06
EGR2 [NCBI] 4.23843e-06
THRB [NCBI] 4.16378e-06
MFN2 [NCBI] 4.09245e-06
SLC5A5 [NCBI] 4.08396e-06
TBX1 [NCBI] 4.02417e-06
DLX3 [NCBI] 3.95869e-06
BTK [NCBI] 3.87473e-06
HOXD13 [NCBI] 3.86527e-06
TGFA [NCBI] 3.77706e-06
PKHD1 [NCBI] 3.74873e-06
SLC26A2 [NCBI] 3.72089e-06
GJB1 [NCBI] 3.64433e-06
EYA1 [NCBI] 3.61424e-06
SOX2 [NCBI] 3.51442e-06
DIO2 [NCBI] 3.46682e-06
CHM [NCBI] 3.46682e-06
SOX10 [NCBI] 3.33224e-06
IGF1 [NCBI] 3.25177e-06
ACCN4 [NCBI] 3.16946e-06
SLC4A1 [NCBI] 3.16946e-06
KRIT1 [NCBI] 3.15028e-06
SDHD [NCBI] 3.07594e-06
GJA1 [NCBI] 2.90481e-06
KAL1 [NCBI] 2.87283e-06
POLG [NCBI] 2.81089e-06
MPZ [NCBI] 2.66666e-06
PAX2 [NCBI] 2.57365e-06
FGF3 [NCBI] 2.52311e-06
MTHFR [NCBI] 2.32359e-06
MTR [NCBI] 2.16414e-06
ATP7A [NCBI] 2.15461e-06
NEFL [NCBI] 1.93633e-06
NGF [NCBI] 1.91864e-06
HLA-DQB1 [NCBI] 1.88608e-06
JAG1 [NCBI] 1.85086e-06
NOTCH3 [NCBI] 1.74987e-06
PTGS2 [NCBI] 1.4989e-06
MEFV [NCBI] 1.11291e-06
CTNNA1 [NCBI] 1.10902e-06
CNTF [NCBI] 1.09363e-06
HLA-DRB1 [NCBI] 1.05283e-06
CHGA [NCBI] 1.04162e-06
NKX2-1 [NCBI] 1.00615e-06
XIAP [NCBI] 9.99218e-07
CAT [NCBI] 8.75906e-07
MECP2 [NCBI] 8.02035e-07
APOE [NCBI] 6.03207e-07
TTR [NCBI] 5.64181e-07
MBP [NCBI] 3.86862e-07
SLC6A4 [NCBI] 3.4443e-07
VHL [NCBI] 2.95032e-07
GSTT1 [NCBI] 2.7026e-07
PTGS1 [NCBI] 2.41996e-07
VWF [NCBI] 2.40252e-07
G6PD [NCBI] 1.4245e-07
GSTM1 [NCBI] 1.38308e-07
TG [NCBI] 4.26188e-08
IL1RN [NCBI] 1.96095e-08
TH [NCBI] 4.83536e-09
NOS3 [NCBI] 1.16298e-09



OMIM


 OMIM Link Information
gain		 01
USH1E [NCBI] 0.00237644
deafness, progressive high-tone neural [NCBI] 0.002306
DFN4 [NCBI] 0.00202379
GJB2 [NCBI] 0.00195389
EVA [NCBI] 0.00190681
USH2B [NCBI] 0.00184937
alport syndrome, autosomal dominant [NCBI] 0.00156248
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss [NCBI] 0.00128245
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy [NCBI] 0.00128245
DFNB15 [NCBI] 0.00114777
SLC26A4 [NCBI] 0.00103493
PDS [NCBI] 0.000988069
FSHMD1A [NCBI] 0.000973992
usher syndrome, type i [NCBI] 0.000876205
DFNA49 [NCBI] 0.00078953
DFNA30 [NCBI] 0.00078953
DFNB20 [NCBI] 0.00078953
DFNA52 [NCBI] 0.00078953
DFNA25 [NCBI] 0.00078953
martin-probst deafness-mental retardation syndrome [NCBI] 0.00078953
DFNB27 [NCBI] 0.00078953
DFNB39 [NCBI] 0.00078953
DFNA16 [NCBI] 0.00078953
DFNB62 [NCBI] 0.00078953
DFNB63 [NCBI] 0.00078953
DFNB14 [NCBI] 0.00078953
DFNA43 [NCBI] 0.00078953
DFNB40 [NCBI] 0.00078953
DFNB17 [NCBI] 0.00078953
DFNA31 [NCBI] 0.00078953
nephropathy, progressive, with deafness [NCBI] 0.00078953
apnea, obstructive sleep [NCBI] 0.000686977
TBS [NCBI] 0.000629599
USH1D [NCBI] 0.000617325
USH3 [NCBI] 0.000581523
MTRNR1 [NCBI] 0.000575088
neuropathy, hereditary sensory and autonomic, type i, with cough and gastroesophageal reflux [NCBI] 0.000572601
otodental dysplasia [NCBI] 0.000572601
DFNA7 [NCBI] 0.000572601
histiocytosis with joint contractures and sensorineural deafness [NCBI] 0.000572601
ALMS [NCBI] 0.000534553
chudley-mccullough syndrome [NCBI] 0.000491365
auditory neuropathy, autosomal dominant, 1 [NCBI] 0.000491365
erythrokeratodermia variabilis 3 [NCBI] 0.000491365
CDH23 [NCBI] 0.000476891
USH2A [NCBI] 0.000474971
KCNQ4 [NCBI] 0.000473213
RA [NCBI] 0.000469236
COCH [NCBI] 0.000462294
MYO7A [NCBI] 0.000460034
HFM [NCBI] 0.000442138
DFNA9 [NCBI] 0.000432082
DFNA2 [NCBI] 0.000418382
USH1C [NCBI] 0.000395919
RP [NCBI] 0.000352381
SALL1 [NCBI] 0.000348882
HMN7A [NCBI] 0.000344358
klippel-feil syndrome, autosomal dominant [NCBI] 0.000322852
oculocerebral syndrome with hypopigmentation [NCBI] 0.000322852
DFNA13 [NCBI] 0.000319937
MTTS1 [NCBI] 0.000310453
visceral neuropathy, familial, autosomal recessive [NCBI] 0.00030418
gonadal dysgenesis, xx type, with deafness [NCBI] 0.00030418
USH2C [NCBI] 0.000298649
DFN2 [NCBI] 0.000287707
optic atrophy 1 and deafness [NCBI] 0.000283128
SLE [NCBI] 0.000282328
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 0.000279065
meniere disease [NCBI] 0.000270255
USH3A [NCBI] 0.000265245
bartter syndrome, infantile, with sensorineural deafness [NCBI] 0.00026052
USH1C [NCBI] 0.000254653
ALMS1 [NCBI] 0.000245457
DFNA12 [NCBI] 0.000243986
MYH9 [NCBI] 0.000243716
WFS1 [NCBI] 0.00023742
DFNA6 [NCBI] 0.000237112
hearing loss, sensorineural, with enamel hypoplasia and nail defects [NCBI] 0.000233854
DFNB59 [NCBI] 0.000233854
renal tubular acidosis, distal, with progressive nerve deafness [NCBI] 0.000230918
DFNB12 [NCBI] 0.00021583
OTOF [NCBI] 0.000208276
USH2A [NCBI] 0.000204707
BJS [NCBI] 0.000203024
DFNB7 [NCBI] 0.000203024
DFNA20 [NCBI] 0.000203024
CF [NCBI] 0.000199405
donnai-barrow syndrome [NCBI] 0.000193012
STL2 [NCBI] 0.000193012
keratoderma, palmoplantar, with deafness [NCBI] 0.000184772
opticoacoustic nerve atrophy with dementia [NCBI] 0.000180123
muenke syndrome [NCBI] 0.000171667
DFNB9 [NCBI] 0.000171667
pejvakin [NCBI] 0.000161663
MTTL1 [NCBI] 0.000157225
STL1 [NCBI] 0.000153552
bsnd gene [NCBI] 0.000150593
CMD1J [NCBI] 0.00014923
cochleosaccular degeneration of the inner ear with progressive cataracts [NCBI] 0.00014923
GJB6 [NCBI] 0.000146245
MTS [NCBI] 0.0001459
OPA1 [NCBI] 0.000142081
TRMA [NCBI] 0.000136915
ACTG1 [NCBI] 0.000136565
insulin-like growth factor i deficiency [NCBI] 0.000135303
USH1G [NCBI] 0.000135303
USH1F [NCBI] 0.000135303
DFNA5 [NCBI] 0.00012718
VEGF [NCBI] 0.000126743
corneal dystrophy and perceptive deafness [NCBI] 0.000125761
DFNA10 [NCBI] 0.000125761
EYA4 [NCBI] 0.000123423
MDM1 [NCBI] 0.000120095
STL3 [NCBI] 0.000118463
DFNA11 [NCBI] 0.000118463
TECTA [NCBI] 0.000114399
DFNA5 [NCBI] 0.000112548
DFNA1 [NCBI] 0.000112548
COL11A2 [NCBI] 0.00011192
PCDH15 [NCBI] 0.000109636
osteogenesis imperfecta, type i [NCBI] 0.000104003
SEDC [NCBI] 0.000103595
DFNA3 [NCBI] 0.000103279
SHFM1 [NCBI] 0.000100718
AD [NCBI] 9.94765e-05
hypoparathyroidism, sensorineural deafness, and renal disease [NCBI] 9.61392e-05
SBS [NCBI] 9.61392e-05
OSMED [NCBI] 9.61392e-05
WHRN [NCBI] 9.51156e-05
MERRF [NCBI] 9.03367e-05
deafness, congenital, with keratopachydermia and constrictions of fingers and toes [NCBI] 9.03367e-05
sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth [NCBI] 9.00379e-05
DFNA28 [NCBI] 9.00379e-05
neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia [NCBI] 9.00379e-05
cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss [NCBI] 9.00379e-05
nephropathy, deafness, and hyperparathyroidism [NCBI] 9.00379e-05
cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness [NCBI] 9.00379e-05
DFNB53 [NCBI] 9.00379e-05
macrothrombocytopenia and progressive sensorineural deafness [NCBI] 9.00379e-05
cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss [NCBI] 9.00379e-05
ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [NCBI] 9.00379e-05
deafness-craniofacial syndrome [NCBI] 9.00379e-05
homozygous 11p15-p14 deletion syndrome [NCBI] 9.00379e-05
USH2D [NCBI] 9.00379e-05
STRC [NCBI] 8.92469e-05
MTTH [NCBI] 8.47543e-05
muckle-wells syndrome [NCBI] 8.32764e-05
marshall syndrome [NCBI] 8.32764e-05
FTNS [NCBI] 8.32764e-05
BCS1L [NCBI] 7.80402e-05
ND [NCBI] 7.49955e-05
SLC19A2 [NCBI] 7.30583e-05
TIMM8A [NCBI] 7.09765e-05
OASD [NCBI] 6.7628e-05
DFNA22 [NCBI] 6.7628e-05
retinitis pigmentosa, deafness, mental retardation, and hypogonadism [NCBI] 6.7628e-05
DFNA44 [NCBI] 6.7628e-05
ermine phenotype [NCBI] 6.7628e-05
deafness, autosomal dominant nonsyndromic sensorineural, due to mutation in myo1a [NCBI] 6.7628e-05
dystonia, juvenile-onset [NCBI] 6.7628e-05
camptodactyly, tall stature, and hearing loss syndrome [NCBI] 6.7628e-05
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies [NCBI] 6.7628e-05
cerebellar ataxia and hypergonadotropic hypogonadism [NCBI] 6.7628e-05
cataract-ataxia-deafness-retardation syndrome [NCBI] 6.7628e-05
deafness-oligodontia syndrome [NCBI] 6.7628e-05
nasodigitoacoustic syndrome [NCBI] 6.7628e-05
myoclonus, cerebellar ataxia, and deafness [NCBI] 6.7628e-05
MELAS [NCBI] 6.61159e-05
COL11A1 [NCBI] 6.58091e-05
MHA [NCBI] 6.49544e-05
DFNB1 [NCBI] 6.49544e-05
LRP2 [NCBI] 6.30007e-05
TBX1 [NCBI] 6.17365e-05
kabuki syndrome [NCBI] 6.14335e-05
SLC4A5 [NCBI] 6.13015e-05
GRHL2 [NCBI] 6.13015e-05
LBX2 [NCBI] 6.13015e-05
TBL1Y [NCBI] 6.13015e-05
P2RY14 [NCBI] 6.13015e-05
OPA1 [NCBI] 6.07241e-05
BOR1 [NCBI] 6.07241e-05
hydrocephalus with cerebellar agenesis [NCBI] 5.92086e-05
DFNB67 [NCBI] 5.92086e-05
DFNA15 [NCBI] 5.92086e-05
DFNA36 [NCBI] 5.92086e-05
DFNB16 [NCBI] 5.92086e-05
deafness, sensorineural, and male infertility [NCBI] 5.92086e-05
DFNB21 [NCBI] 5.92086e-05
coloboma, uveal, with cleft lip and palate and mental retardation [NCBI] 5.92086e-05
DFNB31 [NCBI] 5.92086e-05
ataxia-deafness-retardation syndrome [NCBI] 5.92086e-05
MITF [NCBI] 5.84231e-05
GJB3 [NCBI] 5.46602e-05
brachycephaly, deafness, cataract, microstomia, and mental retardation [NCBI] 5.37631e-05
retinitis pigmentosa-deafness syndrome [NCBI] 5.37631e-05
CMTX5 [NCBI] 5.37631e-05
MG [NCBI] 5.29618e-05
ATS [NCBI] 5.15646e-05
SCS [NCBI] 5.01814e-05
SHEP2 [NCBI] 4.97299e-05
RTADR [NCBI] 4.97299e-05
DFNA17 [NCBI] 4.97299e-05
DFNB6 [NCBI] 4.97299e-05
knuckle pads, leukonychia, and sensorineural deafness [NCBI] 4.97299e-05
WFS1 [NCBI] 4.95153e-05
IGF1 [NCBI] 4.82785e-05
ACCN1 [NCBI] 4.75416e-05
CCDC50 [NCBI] 4.75416e-05
TIMM8B [NCBI] 4.75416e-05
CRMP1 [NCBI] 4.75416e-05
CTNNA2 [NCBI] 4.75416e-05
PFN2 [NCBI] 4.75416e-05
ATOH1 [NCBI] 4.75416e-05
MYO1A [NCBI] 4.75416e-05
charcot-marie-tooth disease and deafness [NCBI] 4.65286e-05
peroxisomal acyl-coa oxidase deficiency [NCBI] 4.65286e-05
charcot-marie-tooth disease, axonal, type 2j [NCBI] 4.65286e-05
DFNB18 [NCBI] 4.65286e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 4.6412e-05
CSA [NCBI] 4.52655e-05
amme complex [NCBI] 4.38769e-05
spondylocarpotarsal synostosis syndrome [NCBI] 4.38769e-05
SANDO [NCBI] 4.38769e-05
LHFPL5 [NCBI] 4.2361e-05
TCF21 [NCBI] 4.2361e-05
SLC4A7 [NCBI] 4.2361e-05
ATP6V0A4 [NCBI] 4.2361e-05
TGFA [NCBI] 4.2361e-05
MTTS2 [NCBI] 4.2361e-05
MTTQ [NCBI] 4.2361e-05
solute carrier family 26 (anion transporter), member 6: slc26a6 [NCBI] 4.2361e-05
CLS [NCBI] 3.92846e-05
MTTL2 [NCBI] 3.9004e-05
ATP2B2 [NCBI] 3.9004e-05
SLC4A11 [NCBI] 3.9004e-05
ATP6V1B1 [NCBI] 3.9004e-05
USH1G [NCBI] 3.9004e-05
EYA2 [NCBI] 3.9004e-05
CATSPER2 [NCBI] 3.9004e-05
POU4F3 [NCBI] 3.9004e-05
CLCNKA [NCBI] 3.9004e-05
deafness, autosomal recessive [NCBI] 3.7905e-05
ACTB [NCBI] 3.65131e-05
MTTW [NCBI] 3.65131e-05
PAX3 [NCBI] 3.63605e-05
epstein syndrome [NCBI] 3.6344e-05
shprintzen-goldberg craniosynostosis syndrome [NCBI] 3.6344e-05
alport syndrome, autosomal recessive [NCBI] 3.49311e-05
COL9A1 [NCBI] 3.45323e-05
WZS [NCBI] 3.36414e-05
LADD [NCBI] 3.36414e-05
CLCNKB [NCBI] 3.28886e-05
TMC1 [NCBI] 3.28886e-05
WS2A [NCBI] 3.2456e-05
COL2A1 [NCBI] 3.1993e-05
PRPS1 [NCBI] 3.14845e-05
TMPRSS3 [NCBI] 3.14845e-05
PEX6 [NCBI] 3.14845e-05
LRS1 [NCBI] 3.03412e-05
MERTK [NCBI] 3.02595e-05
CJD [NCBI] 2.99817e-05
WHS [NCBI] 2.98597e-05
OPD2 [NCBI] 2.93902e-05
POU3F4 [NCBI] 2.91735e-05
DCTN1 [NCBI] 2.91735e-05
DRRS [NCBI] 2.84989e-05
CORD2 [NCBI] 2.84989e-05
ED2 [NCBI] 2.84989e-05
NLRP3 [NCBI] 2.73145e-05
GATA3 [NCBI] 2.73145e-05
MYO6 [NCBI] 2.73145e-05
JLNS1 [NCBI] 2.68698e-05
osteogenesis imperfecta, type iv [NCBI] 2.68698e-05
PBD [NCBI] 2.4738e-05
osteogenesis imperfecta, type iii [NCBI] 2.4738e-05
SLSN1 [NCBI] 2.4738e-05
deafness, conductive, with stapes fixation [NCBI] 2.4738e-05
SALL4 [NCBI] 2.44293e-05
canavan disease [NCBI] 2.34829e-05
ACLS [NCBI] 2.28971e-05
EGR2 [NCBI] 2.27325e-05
ZS [NCBI] 2.26212e-05
KAL2 [NCBI] 2.23363e-05
refsum disease, infantile form [NCBI] 2.23363e-05
biotinidase deficiency [NCBI] 2.17986e-05
CFNS [NCBI] 2.0786e-05
SDHD [NCBI] 2.04582e-05
LCA1 [NCBI] 2.03083e-05
EKV [NCBI] 1.98481e-05
TWIST1 [NCBI] 1.96878e-05
BDNF [NCBI] 1.91676e-05
PFIC1 [NCBI] 1.85617e-05
HCH [NCBI] 1.85617e-05
PMP22 [NCBI] 1.82329e-05
FCAS [NCBI] 1.81613e-05
mannosidosis, alpha b, lysosomal [NCBI] 1.77738e-05
EVC [NCBI] 1.70345e-05
PHEX [NCBI] 1.68703e-05
KSS [NCBI] 1.67546e-05
NDP [NCBI] 1.66071e-05
ASPA [NCBI] 1.63517e-05
POLG [NCBI] 1.58631e-05
PGL1 [NCBI] 1.53691e-05
down syndrome [NCBI] 1.39194e-05
AVP [NCBI] 1.3796e-05
FGFR3 [NCBI] 1.33118e-05
KCNQ1 [NCBI] 1.32421e-05
DGS [NCBI] 1.2912e-05
adrenoleukodystrophy, autosomal neonatal form [NCBI] 1.28859e-05
WS1 [NCBI] 1.10893e-05
NF2 [NCBI] 1.04932e-05
velocardiofacial syndrome [NCBI] 9.40652e-06
MPZ [NCBI] 8.63148e-06
BTK [NCBI] 8.02075e-06
TD1 [NCBI] 7.99799e-06
SVAS [NCBI] 7.44367e-06
INSR [NCBI] 7.23939e-06
TH [NCBI] 7.03441e-06
MECP2 [NCBI] 5.7587e-06
TG [NCBI] 4.12338e-06
fabry disease [NCBI] 3.83618e-06
ACH [NCBI] 3.6906e-06
G6PD [NCBI] 3.59352e-06
MBP [NCBI] 3.09001e-06
NGFB [NCBI] 7.65282e-07
CVID [NCBI] 7.30325e-07
CNTF [NCBI] 5.66976e-07
AS [NCBI] 5.38353e-07
CAT [NCBI] 3.79769e-07
TTR [NCBI] 2.13268e-07
temporal arteritis [NCBI] 1.70771e-07
XDH [NCBI] 1.08897e-07
GDNF [NCBI] 3.53766e-08



Database Center for Life Science