|
OMIM |
Link |
Information gain |
01 |
|
microtia with meatal atresia and conductive deafness
|
[NCBI]
|
0.00306599
|
|
|
johnson neuroectodermal syndrome
|
[NCBI]
|
0.00156207
|
|
|
microtia-anotia
|
[NCBI]
|
0.00146918
|
|
|
OTSC4
|
[NCBI]
|
0.000993831
|
|
|
atresia of external auditory canal and conduction deafness
|
[NCBI]
|
0.000776146
|
|
|
branchiootic syndrome 2
|
[NCBI]
|
0.000694153
|
|
|
earlobes, thickened, with conductive deafness from incudostapedial abnormalities
|
[NCBI]
|
0.000694153
|
|
|
OSCS
|
[NCBI]
|
0.000570168
|
|
|
klippel-feil syndrome, autosomal dominant
|
[NCBI]
|
0.000521852
|
|
|
OTSC1
|
[NCBI]
|
0.000469717
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000431005
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.00042004
|
|
|
EEC1
|
[NCBI]
|
0.000289233
|
|
|
stapes ankylosis with broad thumb and toes
|
[NCBI]
|
0.000199048
|
|
|
HFM
|
[NCBI]
|
0.000170403
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
0.000156776
|
|
|
SYNS1
|
[NCBI]
|
0.000153596
|
|
|
SYM1
|
[NCBI]
|
0.000151004
|
|
|
NOG
|
[NCBI]
|
0.000132035
|
|
|
ossicular malformations, familial
|
[NCBI]
|
0.00012182
|
|
|
deafness, conductive stapedial, with ear malformation and facial palsy
|
[NCBI]
|
0.00012182
|
|
|
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia
|
[NCBI]
|
9.93556e-05
|
|
|
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies
|
[NCBI]
|
9.93556e-05
|
|
|
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia
|
[NCBI]
|
9.93556e-05
|
|
|
epiphyseal dysplasia, multiple, with myopia and conductive deafness
|
[NCBI]
|
9.93556e-05
|
|
|
FOP
|
[NCBI]
|
9.38487e-05
|
|
|
branchial arch syndrome, x-linked
|
[NCBI]
|
8.53826e-05
|
|
|
gombo syndrome
|
[NCBI]
|
8.53826e-05
|
|
|
zunich neuroectodermal syndrome
|
[NCBI]
|
7.80401e-05
|
|
|
DFNA1
|
[NCBI]
|
7.53344e-05
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
6.92003e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
6.61183e-05
|
|
|
POU3F4
|
[NCBI]
|
6.58157e-05
|
|
|
OPD1
|
[NCBI]
|
6.2385e-05
|
|
|
LRS1
|
[NCBI]
|
6.13123e-05
|
|
|
EYA1
|
[NCBI]
|
5.81716e-05
|
|
|
SOST
|
[NCBI]
|
5.76247e-05
|
|
|
CMDD
|
[NCBI]
|
5.68226e-05
|
|
|
MNS
|
[NCBI]
|
5.53307e-05
|
|
|
SLE
|
[NCBI]
|
5.49151e-05
|
|
|
BWS
|
[NCBI]
|
5.0311e-05
|
|
|
BOR1
|
[NCBI]
|
4.99544e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
4.94565e-05
|
|
|
DA2A
|
[NCBI]
|
4.85058e-05
|
|
|
COL2A1
|
[NCBI]
|
4.5107e-05
|
|
|
FDH
|
[NCBI]
|
4.4467e-05
|
|
|
down syndrome
|
[NCBI]
|
4.31066e-05
|
|
|
hypophosphatemic rickets, x-linked dominant
|
[NCBI]
|
4.24691e-05
|
|
|
MECP2
|
[NCBI]
|
3.99763e-05
|
|
|
TCOF
|
[NCBI]
|
3.81473e-05
|
|
|
GJB2
|
[NCBI]
|
3.77812e-05
|
|
|
AMC
|
[NCBI]
|
3.76845e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
3.74583e-05
|
|
|
CCD
|
[NCBI]
|
3.44216e-05
|
|
|
PCD
|
[NCBI]
|
2.38817e-05
|
|
|
CF
|
[NCBI]
|
2.13417e-05
|
|
|
PTH
|
[NCBI]
|
7.9829e-06
|
|
|
RA
|
[NCBI]
|
3.94249e-06
|
|