| # |
|
Family |
MCID |
Name |
MIFTS |
Score |
| 1 |
|
c
|
HPT073 |
Hepatitis C Virus |
70 |
16.117 |
|
| 2 |
|
c
|
LKD010 |
Leukodystrophy, Hypomyelinating, 2 |
51 |
9.097 |
|
|
| 3 |
|
|
CNV004 |
Canavan Disease |
65 |
9.097 |
|
|
| 4 |
|
P
|
BRS047 |
Breast Cancer |
97 |
0.810 |
|
|
| 5 |
|
P
|
PNC035 |
Pancreatic Cancer |
91 |
0.573 |
|
|
| 6 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
0.573 |
|
|
| 7 |
|
c
|
CRD184 |
Ceroid Lipofuscinosis, Neuronal, 5 |
59 |
0.476 |
|
|
| 8 |
|
c
|
HYP595 |
Hypertension, Essential |
86 |
0.476 |
|
|
| 9 |
|
P
|
NRB001 |
Neuroblastoma |
62 |
0.402 |
|
|
| 10 |
|
c
|
NPH055 |
Nephrotic Syndrome, Type 1 |
57 |
0.312 |
|
|
| 11 |
|
|
SKN022 |
Skin Squamous Cell Carcinoma |
61 |
0.255 |
|
|
| 12 |
|
P
|
SKN015 |
Skin Carcinoma |
67 |
0.255 |
|
|
| 13 |
|
|
CMB022 |
Combined Cellular and Humoral Immune Defects with Granulomas |
42 |
0.180 |
|
|
| 14 |
|
P
|
HNT016 |
Huntington Disease |
72 |
0.180 |
|
|
| 15 |
|
P
|
MCH002 |
Machado-Joseph Disease |
63 |
0.180 |
|
|
| 16 |
|
c
|
ACH033 |
Achondrogenesis, Type Ia |
49 |
0.180 |
|
|
| 17 |
|
|
ACY010 |
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of |
65 |
0.180 |
|
|
| 18 |
|
|
CHR629 |
Charcot-Marie-Tooth Disease and Deafness |
58 |
0.180 |
|
|
| 19 |
|
c
|
CWD006 |
Cowden Syndrome 1 |
78 |
0.180 |
|
|
| 20 |
|
P
|
BTH005 |
Bethlem Myopathy 1 |
64 |
0.180 |
|
|
| 21 |
|
|
ADR042 |
Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency |
54 |
0.180 |
|
|
| 22 |
|
P
|
KRB001 |
Krabbe Disease |
69 |
0.180 |
|
|
| 23 |
|
|
MLY008 |
Molybdenum Cofactor Deficiency, Complementation Group a |
50 |
0.180 |
|
|
| 24 |
|
|
WDM004 |
Wiedemann-Steiner Syndrome |
50 |
0.180 |
|
|
| 25 |
|
|
SVR096 |
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative |
55 |
0.180 |
|
|
