# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
P
|
BRS047 |
Breast Cancer |
97 |
18.595 |
|
2 |
|
c
|
BSL024 |
Basal Cell Carcinoma 1 |
59 |
15.969 |
|
3 |
|
P
|
CPL014 |
Capillary Malformation-Arteriovenous Malformation 1 |
57 |
15.969 |
|
4 |
|
c
|
BSL011 |
Basal Cell Carcinoma, Multiple |
26 |
15.969 |
|
5 |
|
|
TRC096 |
Trichothiodystrophy |
55 |
11.471 |
|
6 |
|
|
XRD010 |
Xeroderma Pigmentosum, Variant Type |
72 |
11.312 |
|
7 |
|
P
|
CCK001 |
Cockayne Syndrome |
67 |
11.312 |
|
8 |
|
|
TSY002 |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations |
56 |
7.999 |
|
9 |
|
c
|
XRD023 |
Xeroderma Pigmentosum, Complementation Group G |
54 |
7.999 |
|
10 |
|
c
|
XRD022 |
Xeroderma Pigmentosum, Complementation Group D |
56 |
7.999 |
|
11 |
|
c
|
XRD032 |
Xeroderma Pigmentosum, Complementation Group B |
49 |
7.999 |
|
12 |
|
|
KLP010 |
Klippel-Trenaunay-Weber Syndrome |
61 |
7.971 |
|
13 |
|
c
|
TLN006 |
Telangiectasia, Hereditary Hemorrhagic, Type 1 |
58 |
7.971 |
|
14 |
|
|
HMN027 |
Hemangioma, Capillary Infantile |
38 |
7.971 |
|
15 |
|
P
|
HRD008 |
Hereditary Hemorrhagic Telangiectasia |
64 |
7.971 |
|
16 |
|
|
ANG062 |
Angioosteohypertrophic Syndrome |
45 |
7.971 |
|
17 |
|
|
ESP021 |
Esophageal Cancer |
83 |
1.618 |
|
18 |
|
|
SQM006 |
Squamous Cell Carcinoma |
57 |
1.580 |
|
19 |
|
|
ESP027 |
Esophagus Squamous Cell Carcinoma |
58 |
1.580 |
|
20 |
|
|
THY029 |
Thyroid Carcinoma |
52 |
1.313 |
|
21 |
|
P
|
OVR042 |
Ovarian Cancer |
89 |
0.710 |
|
22 |
|
P
|
PNC035 |
Pancreatic Cancer |
91 |
0.550 |
|
23 |
|
P
|
LKM062 |
Leukemia, Acute Lymphoblastic |
69 |
0.550 |
|
24 |
|
P
|
PRP019 |
Peripheral Nervous System Disease |
63 |
0.479 |
|
25 |
|
P
|
NRP001 |
Neuropathy |
58 |
0.479 |
|