# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
|
CHR629 |
Charcot-Marie-Tooth Disease and Deafness |
58 |
48.319 |
|
2 |
|
P
|
NRP063 |
Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
66 |
42.279 |
|
3 |
|
c
|
CHR653 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1d |
41 |
41.715 |
|
4 |
|
|
HYP186 |
Hypertrophic Neuropathy of Dejerine-Sottas |
54 |
38.564 |
|
5 |
|
P
|
CHR071 |
Charcot-Marie-Tooth Disease |
64 |
29.290 |
|
6 |
|
P
|
NRP001 |
Neuropathy |
58 |
18.394 |
|
7 |
|
|
TTH006 |
Tooth Disease |
47 |
17.699 |
|
8 |
|
P
|
CHR654 |
Charcot-Marie-Tooth Disease, Axonal, Type 2e |
67 |
13.279 |
|
9 |
|
P
|
PLY019 |
Polyneuropathy |
53 |
11.567 |
|
10 |
|
P
|
SCL018 |
Scoliosis |
56 |
11.554 |
|
11 |
|
|
SNS003 |
Sensory Peripheral Neuropathy |
51 |
10.890 |
|
12 |
|
P
|
RTT002 |
Rett Syndrome |
78 |
10.844 |
|
13 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
63 |
9.474 |
|
14 |
|
P
|
DMY001 |
Demyelinating Polyneuropathy |
46 |
8.525 |
|
15 |
|
c
|
CHR627 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1a |
58 |
8.470 |
|
16 |
|
|
NRP051 |
Neuropathy, Hereditary, with Liability to Pressure Palsies |
57 |
8.389 |
|
17 |
|
P
|
CHR640 |
Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 |
60 |
8.351 |
|
18 |
|
P
|
HRS035 |
Hirschsprung Disease 1 |
69 |
7.854 |
|
19 |
|
|
NRM005 |
Neuromuscular Disease |
63 |
7.805 |
|
20 |
|
P
|
CHR625 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1b |
59 |
7.412 |
|
21 |
|
c
|
CHR517 |
Charcot-Marie-Tooth Disease, Type 4a |
49 |
7.241 |
|
22 |
|
c
|
CHR647 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1c |
48 |
7.170 |
|
23 |
|
c
|
CHR516 |
Charcot-Marie-Tooth Disease, Type 4c |
51 |
7.141 |
|
24 |
|
c
|
CHR519 |
Charcot-Marie-Tooth Disease, Type 4b2 |
51 |
7.071 |
|
25 |
|
c
|
CHR376 |
Charcot-Marie-Tooth Disease, Type 4d |
50 |
7.071 |
|