|
OMIM |
Link |
Information gain |
01 |
|
HFM
|
[NCBI]
|
0.00941662
|
|
|
microtia with meatal atresia and conductive deafness
|
[NCBI]
|
0.00655293
|
|
|
microtia-anotia
|
[NCBI]
|
0.00618408
|
|
|
auriculocondylar syndrome
|
[NCBI]
|
0.0039641
|
|
|
hypertelorism, microtia, facial clefting syndrome
|
[NCBI]
|
0.00257433
|
|
|
preauricular fistulae, congenital
|
[NCBI]
|
0.00232632
|
|
|
aural atresia, congenital
|
[NCBI]
|
0.00204776
|
|
|
TBS
|
[NCBI]
|
0.00165039
|
|
|
earlobes, thickened, with conductive deafness from incudostapedial abnormalities
|
[NCBI]
|
0.0016217
|
|
|
preauricular tag, isolated, autosomal dominant, 1
|
[NCBI]
|
0.00102222
|
|
|
diamond-blackfan anemia with microtia and cleft palate
|
[NCBI]
|
0.00102222
|
|
|
actinic prurigo
|
[NCBI]
|
0.00102222
|
|
|
ear malformation
|
[NCBI]
|
0.00102222
|
|
|
ear, patella, short stature syndrome
|
[NCBI]
|
0.000898584
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.000898584
|
|
|
earlobe crease
|
[NCBI]
|
0.000870111
|
|
|
LADD
|
[NCBI]
|
0.000830476
|
|
|
charge syndrome
|
[NCBI]
|
0.000801044
|
|
|
hairy ears, y-linked
|
[NCBI]
|
0.000793577
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000727254
|
|
|
deafness, conductive, with malformed external ear
|
[NCBI]
|
0.000713579
|
|
|
otoonychoperoneal syndrome
|
[NCBI]
|
0.000713579
|
|
|
BOR1
|
[NCBI]
|
0.000634027
|
|
|
nablus mask-like facial syndrome
|
[NCBI]
|
0.000598547
|
|
|
hypoadrenocorticism, familial
|
[NCBI]
|
0.000598547
|
|
|
branchiootic syndrome 2
|
[NCBI]
|
0.000524669
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000477757
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.000470337
|
|
|
hairy ears
|
[NCBI]
|
0.000457622
|
|
|
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth
|
[NCBI]
|
0.000427518
|
|
|
dermatitis, atopic
|
[NCBI]
|
0.000427518
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
0.0003625
|
|
|
earlobe attachment: attached vs unattached
|
[NCBI]
|
0.000347271
|
|
|
ZLS
|
[NCBI]
|
0.000336737
|
|
|
AMCN
|
[NCBI]
|
0.000336737
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000336737
|
|
|
MCOPS1
|
[NCBI]
|
0.000336737
|
|
|
BOS1
|
[NCBI]
|
0.000330649
|
|
|
charge-like syndrome, x-linked
|
[NCBI]
|
0.00029323
|
|
|
ear pits, posterior helical
|
[NCBI]
|
0.00029323
|
|
|
CES
|
[NCBI]
|
0.000282571
|
|
|
isotretinoin embryopathy-like syndrome
|
[NCBI]
|
0.000268839
|
|
|
say syndrome
|
[NCBI]
|
0.000268839
|
|
|
SLE
|
[NCBI]
|
0.000194909
|
|
|
RA
|
[NCBI]
|
0.000193733
|
|
|
SALL1
|
[NCBI]
|
0.000189115
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
0.000174837
|
|
|
NHS
|
[NCBI]
|
0.00017373
|
|
|
ossified ear cartilages
|
[NCBI]
|
0.000173508
|
|
|
arthrogryposis, distal, type 2e
|
[NCBI]
|
0.000173508
|
|
|
speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe crease
|
[NCBI]
|
0.000173508
|
|
|
simosa craniofacial syndrome
|
[NCBI]
|
0.000173508
|
|
|
cryptotia, familial
|
[NCBI]
|
0.000173508
|
|
|
ear folding
|
[NCBI]
|
0.000173508
|
|
|
aurocephalosyndactyly
|
[NCBI]
|
0.000173508
|
|
|
deafness, conductive stapedial, with ear malformation and facial palsy
|
[NCBI]
|
0.000173508
|
|
|
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes
|
[NCBI]
|
0.000173508
|
|
|
microcephaly-cardiomyopathy
|
[NCBI]
|
0.000173508
|
|
|
ABS
|
[NCBI]
|
0.000170352
|
|
|
BWS
|
[NCBI]
|
0.000147838
|
|
|
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia
|
[NCBI]
|
0.000134293
|
|
|
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia
|
[NCBI]
|
0.000134293
|
|
|
radial-renal syndrome
|
[NCBI]
|
0.000134293
|
|
|
OAFNS
|
[NCBI]
|
0.000134293
|
|
|
deafness, congenital, with inner ear agenesis, microtia, and microdontia
|
[NCBI]
|
0.000134293
|
|
|
creases, infra-auricular cutaneous, with tall stature and advanced bone age
|
[NCBI]
|
0.000134293
|
|
|
split-foot deformity with mandibulofacial dysostosis
|
[NCBI]
|
0.00011953
|
|
|
brachycephaly, deafness, cataract, microstomia, and mental retardation
|
[NCBI]
|
0.00011953
|
|
|
EEC1
|
[NCBI]
|
0.000117993
|
|
|
native american myopathy
|
[NCBI]
|
0.000109964
|
|
|
intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
|
[NCBI]
|
0.000109964
|
|
|
mental retardation, fra12a type
|
[NCBI]
|
0.000102867
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
0.000102867
|
|
|
poland syndrome
|
[NCBI]
|
0.000101844
|
|
|
NHS
|
[NCBI]
|
9.88362e-05
|
|
|
palatopharyngeal incompetence
|
[NCBI]
|
9.69674e-05
|
|
|
tetralogy of fallot
|
[NCBI]
|
8.8542e-05
|
|
|
rokitansky-kuster-hauser syndrome
|
[NCBI]
|
8.19603e-05
|
|
|
corpus callosum, agenesis of
|
[NCBI]
|
7.91841e-05
|
|
|
ACG2
|
[NCBI]
|
7.91841e-05
|
|
|
ALSG
|
[NCBI]
|
7.66667e-05
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
7.57259e-05
|
|
|
OPD2
|
[NCBI]
|
7.2245e-05
|
|
|
COFS1
|
[NCBI]
|
7.2245e-05
|
|
|
GACI
|
[NCBI]
|
6.8453e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
6.67429e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
6.51372e-05
|
|
|
AFD1
|
[NCBI]
|
6.36242e-05
|
|
|
SGBS1
|
[NCBI]
|
5.60352e-05
|
|
|
AHC
|
[NCBI]
|
5.01993e-05
|
|
|
DGS
|
[NCBI]
|
5.00597e-05
|
|
|
SCS
|
[NCBI]
|
4.62073e-05
|
|
|
CCM
|
[NCBI]
|
4.34296e-05
|
|
|
MATN1
|
[NCBI]
|
4.1979e-05
|
|
|
GPRK6
|
[NCBI]
|
4.1979e-05
|
|
|
ALGS1
|
[NCBI]
|
3.8699e-05
|
|
|
LYZ
|
[NCBI]
|
3.73219e-05
|
|
|
TFPI
|
[NCBI]
|
3.68549e-05
|
|
|
SMAD3
|
[NCBI]
|
3.50017e-05
|
|
|
CDLS1
|
[NCBI]
|
3.07091e-05
|
|
|
DBA
|
[NCBI]
|
2.82657e-05
|
|
|
FGF10
|
[NCBI]
|
2.81898e-05
|
|
|
WHS
|
[NCBI]
|
2.41303e-05
|
|
|
FGF1
|
[NCBI]
|
2.19978e-05
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
2.16501e-05
|
|
|
PLG
|
[NCBI]
|
2.07692e-05
|
|
|
krabbe disease
|
[NCBI]
|
1.9476e-05
|
|
|
CDK4
|
[NCBI]
|
1.87719e-05
|
|
|
INS
|
[NCBI]
|
1.5595e-05
|
|
|
CDK2
|
[NCBI]
|
1.53827e-05
|
|
|
GJA1
|
[NCBI]
|
1.25713e-05
|
|
|
NPY
|
[NCBI]
|
1.20158e-05
|
|
|
HGF
|
[NCBI]
|
1.05964e-05
|
|
|
FGF7
|
[NCBI]
|
1.0336e-05
|
|
|
VEGF
|
[NCBI]
|
9.8518e-06
|
|
|
MPO
|
[NCBI]
|
9.7517e-06
|
|
|
PCNA
|
[NCBI]
|
8.85139e-06
|
|
|
MBP
|
[NCBI]
|
2.05694e-06
|
|
|
EGF
|
[NCBI]
|
1.59332e-06
|
|
|
TH
|
[NCBI]
|
2.27869e-07
|
|
|
TNF
|
[NCBI]
|
1.53229e-07
|
|
|
SRS
|
[NCBI]
|
3.22056e-08
|
|