# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
c
|
DFN190 |
Deafness, Autosomal Dominant 2a |
38 |
44.217 |
|
2 |
|
|
DFN001 |
Dfna2 Nonsyndromic Hearing Loss |
13 |
31.246 |
|
3 |
|
P
|
NNS072 |
Nonsyndromic Hearing Loss |
43 |
23.370 |
|
4 |
|
|
RRG078 |
Rare Genetic Deafness |
37 |
22.105 |
|
5 |
|
|
NNS044 |
Non-Syndromic Genetic Deafness |
44 |
20.683 |
|
6 |
|
P
|
SNS001 |
Sensorineural Hearing Loss |
59 |
19.157 |
|
7 |
|
|
DFN245 |
Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct |
53 |
9.626 |
|
8 |
|
P
|
LNG028 |
Long Qt Syndrome |
63 |
8.511 |
|
9 |
|
c
|
DFN136 |
Deafness, Autosomal Dominant 9 |
46 |
8.426 |
|
10 |
|
c
|
LNG044 |
Long Qt Syndrome 1 |
67 |
8.381 |
|
11 |
|
|
ATS251 |
Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna |
27 |
8.222 |
|
12 |
|
c
|
ATS005 |
Autosomal Dominant Nonsyndromic Deafness |
27 |
7.835 |
|
13 |
|
|
BNG006 |
Benign Familial Neonatal Epilepsy |
53 |
7.155 |
|
14 |
|
P
|
BNG026 |
Benign Neonatal Seizures |
51 |
7.155 |
|
15 |
|
|
MNR012 |
Meniere Disease |
56 |
6.962 |
|
16 |
|
c
|
DFN097 |
Deafness, Autosomal Recessive 1a |
51 |
6.914 |
|
17 |
|
c
|
BRN131 |
Branchiootorenal Syndrome 1 |
46 |
6.914 |
|
18 |
|
c
|
USH036 |
Usher Syndrome, Type I |
63 |
6.851 |
|
19 |
|
c
|
DFN196 |
Deafness, Autosomal Dominant 22 |
45 |
6.851 |
|
20 |
|
P
|
CNT116 |
Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a |
54 |
6.732 |
|
21 |
|
c
|
WRD030 |
Waardenburg Syndrome, Type 1 |
55 |
6.699 |
|
22 |
|
c
|
DFN118 |
Deafness, Autosomal Dominant 44 |
29 |
6.699 |
|
23 |
|
c
|
DFN165 |
Deafness, Autosomal Recessive 14 |
19 |
6.699 |
|
24 |
|
c
|
DFN107 |
Deafness, Autosomal Dominant 10 |
40 |
6.699 |
|
25 |
|
c
|
DFN155 |
Deafness, Autosomal Dominant 41 |
34 |
6.699 |
|