|
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
|
|