| # |
|
Family |
MCID |
Name |
MIFTS |
Score |
| 51 |
|
P
|
CNR004 |
Cone-Rod Dystrophy 2 |
78 |
0.282 |
|
| 52 |
|
P
|
EPL140 |
Epilepsy, Idiopathic Generalized |
61 |
0.282 |
|
|
| 53 |
|
P
|
EPL164 |
Epilepsy |
71 |
0.282 |
|
|
| 54 |
|
P
|
ADN016 |
Adenocarcinoma |
64 |
0.282 |
|
|
| 55 |
|
|
ENH001 |
Enhanced S-Cone Syndrome |
59 |
0.231 |
|
|
| 56 |
|
|
PLM129 |
Pulmonary Disease, Chronic Obstructive |
74 |
0.231 |
|
|
| 57 |
|
|
ATX019 |
Ataxia with Vitamin E Deficiency |
61 |
0.231 |
|
|
| 58 |
|
|
FCL014 |
Focal Epilepsy |
53 |
0.231 |
|
|
| 59 |
|
c
|
SML038 |
Small Cell Cancer of the Lung |
68 |
0.163 |
|
|
| 60 |
|
c
|
HYP331 |
Hyperphenylalaninemia, Bh4-Deficient, a |
71 |
0.163 |
|
|
| 61 |
|
c
|
HYP595 |
Hypertension, Essential |
86 |
0.163 |
|
|
| 62 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
66 |
0.163 |
|
|
| 63 |
|
|
ADL002 |
Adult Syndrome |
68 |
0.163 |
|
|
| 64 |
|
P
|
CLB034 |
Coloboma, Ocular, Autosomal Dominant |
53 |
0.163 |
|
|
| 65 |
|
|
CRN048 |
Craniofacial-Deafness-Hand Syndrome |
48 |
0.163 |
|
|
| 66 |
|
|
OBS002 |
Obsessive-Compulsive Disorder |
67 |
0.163 |
|
|
| 67 |
|
P
|
OVR042 |
Ovarian Cancer |
89 |
0.163 |
|
|
| 68 |
|
|
MYC079 |
Myoclonic Epilepsy of Lafora |
64 |
0.163 |
|
|
| 69 |
|
c
|
LKM061 |
Leukemia, Acute Myeloid |
82 |
0.163 |
|
|
| 70 |
|
c
|
EPL200 |
Epilepsy, Childhood Absence 1 |
31 |
0.163 |
|
|
| 71 |
|
c
|
FNC043 |
Fanconi Anemia, Complementation Group E |
68 |
0.163 |
|
|
| 72 |
|
P
|
MJR001 |
Major Depressive Disorder |
75 |
0.163 |
|
|
| 73 |
|
|
STR067 |
Stroke, Ischemic |
81 |
0.163 |
|
|
| 74 |
|
c
|
NPH054 |
Nephrotic Syndrome, Type 3 |
42 |
0.163 |
|
|
| 75 |
|
|
SPT022 |
Spitzoid Melanoma |
35 |
0.163 |
|
|
