# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
c
|
PLM128 |
Pulmonary Hypertension, Primary, 2 |
33 |
39.017 |
|
2 |
|
P
|
PLM037 |
Pulmonary Hypertension |
73 |
11.811 |
|
3 |
|
P
|
CHR654 |
Charcot-Marie-Tooth Disease, Axonal, Type 2e |
67 |
11.281 |
|
4 |
|
c
|
PLM164 |
Pulmonary Hypertension, Primary, 1 |
76 |
10.684 |
|
5 |
|
P
|
OST002 |
Osteoporosis |
82 |
10.471 |
|
6 |
|
|
HRT015 |
Heritable Pulmonary Arterial Hypertension |
45 |
10.404 |
|
7 |
|
c
|
NRP053 |
Neuropathy, Hereditary Sensory and Autonomic, Type Iia |
69 |
9.211 |
|
8 |
|
|
CLF027 |
Cleft Palate, Isolated |
63 |
9.211 |
|
9 |
|
|
SPN028 |
Spondyloepimetaphyseal Dysplasia, Strudwick Type |
58 |
9.211 |
|
10 |
|
|
CHR619 |
Chromosome 2q35 Duplication Syndrome |
62 |
9.211 |
|
11 |
|
P
|
NRP063 |
Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
66 |
9.211 |
|
12 |
|
P
|
DST002 |
Distal Arthrogryposis |
61 |
9.211 |
|
13 |
|
|
PLM184 |
Pulmonary Arterial Hypertension Associated with Congenital Heart Disease |
35 |
9.043 |
|
14 |
|
P
|
ART005 |
Arteriovenous Malformation |
65 |
6.855 |
|
15 |
|
P
|
PLM025 |
Pulmonary Venoocclusive Disease |
48 |
6.778 |
|
16 |
|
P
|
HRD008 |
Hereditary Hemorrhagic Telangiectasia |
64 |
6.666 |
|
17 |
|
|
CRY035 |
Cryptorchidism, Unilateral or Bilateral |
60 |
6.513 |
|
18 |
|
P
|
TTR001 |
Tetralogy of Fallot |
70 |
6.513 |
|
19 |
|
P
|
STR020 |
Strabismus |
57 |
6.513 |
|
20 |
|
P
|
CNR004 |
Cone-Rod Dystrophy 2 |
78 |
6.513 |
|
21 |
|
|
EPP022 |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness |
35 |
6.513 |
|
22 |
|
P
|
PTN014 |
Patent Ductus Arteriosus 1 |
59 |
6.513 |
|
23 |
|
|
CNZ006 |
Coenzyme Q10 Deficiency, Primary, 1 |
43 |
6.513 |
|
24 |
|
c
|
CHR641 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 |
38 |
6.513 |
|
25 |
|
c
|
CLR134 |
Ciliary Dyskinesia, Primary, 3 |
42 |
6.513 |
|