Search results for cap2

51 hits were found for cap2

# Family MCID Name MIFTS Score
1
FML304 Familial Isolated Dilated Cardiomyopathy 49 9.407
2
c DLT002 Dilated Cardiomyopathy 78 5.265
3
CRD132 Cardiac Conduction Defect 60 4.759
4
P GST053 Gastric Cancer 83 4.707
5
c ATR087 Atrial Standstill 1 74 4.516
6
P MLN008 Melanoma 76 4.447
7
P HPT023 Hepatocellular Carcinoma 96 3.862
8
P OVR042 Ovarian Cancer 88 3.187
9
GLL048 Glial Tumor 52 3.027
10
GLM045 Glioma 63 3.027
11
MCR013 Microphthalmia 60 2.913
12
OVR094 Ovarian Epithelial Cancer 39 2.614
13
NDL001 Nodular Malignant Melanoma 45 2.420
14
P MYP004 Myopathy 67 2.380
15
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.317
16
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.317
17
c MJR022 Major Affective Disorder 8 38 2.215
18
c MJR024 Major Affective Disorder 9 41 2.215
19
P BPL003 Bipolar Disorder 56 2.215
20
TRN015 Transient Cerebral Ischemia 63 2.095
21
P VSC007 Vascular Disease 63 2.095
22
P PNM007 Pneumonia 67 1.562
23
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 1.442
24
P LNG021 Lung Occult Small Cell Carcinoma 20 1.442
25
LNG019 Lung Combined Type Small Cell Carcinoma 32 1.442
26
P PNC035 Pancreatic Cancer 86 1.272
27
ALL029 Allergic Disease 59 1.210
28
P BND020 Bone Disease 59 1.210
29
P HRP006 Herpes Simplex 65 0.988
30
P RNV001 Renovascular Hypertension 49 0.988
31
P ATR011 Atrial Fibrillation 66 0.857
32
c FML001 Familial Atrial Fibrillation 65 0.857
33
P BRS047 Breast Cancer 98 0.811
34
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.698
35
c DFN137 Deafness, Autosomal Dominant 13 32 0.698
36
c DFN154 Deafness, Autosomal Dominant 31 22 0.698
37
PRP027 Peripheral Vascular Disease 71 0.698
38
ALV005 Alveolar Soft Part Sarcoma 61 0.698
39
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.698
40
MYL005 Myelofibrosis 71 0.698
41
PLY001 Polycythemia Vera 69 0.698
42
P PRS040 Prostate Cancer 95 0.698
43
c DFN150 Deafness, Autosomal Dominant 21 24 0.698
44
TRM010 Traumatic Brain Injury 51 0.698
45
P PLY018 Polycythemia 56 0.698
46
CMB007 Combined Immunodeficiency 57 0.698
47
P ESS003 Essential Thrombocythemia 69 0.698
48
CNG034 Congestive Heart Failure 69 0.698
49
SVR004 Severe Combined Immunodeficiency 72 0.698
50
CHL068 Cholestasis 61 0.698
51
BRN071 Brain Injury 50 0.698
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