Search results for vcl

77 hits were found for vcl

# Family MCID Name MIFTS Score
1
c VCL003 Vcl-Related Dilated Cardiomyopathy 11 9.634
2
c VCL006 Vcl-Related Familial Hypertrophic Cardiomyopathy 11 9.634
3
c DLT002 Dilated Cardiomyopathy 76 5.150
4
P CRD011 Cardiomyopathy 68 5.150
5
c CRD092 Cardiomyopathy, Dilated, 1w 22 4.889
6
c CRD200 Cardiomyopathy, Hypertrophic, 15 28 4.523
7
BCK001 Becker Muscular Dystrophy 69 4.296
8
DRR010 Darier Disease 60 4.296
9
SHG001 Shigellosis 54 4.296
10
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 3.900
11
DCH001 Duchenne Muscular Dystrophy 79 3.843
12
CRB011 Cerebrotendinous Xanthomatosis 61 3.843
13
XNT003 Xanthomatosis 46 3.843
14
FML304 Familial Isolated Dilated Cardiomyopathy 31 3.362
15
CNG034 Congestive Heart Failure 72 3.328
16
QBC001 Quebec Platelet Disorder 48 3.328
17
GRV012 Grover's Disease 36 3.328
18
CHL010 Childhood Kidney Cell Carcinoma 33 3.328
19
ACT056 Acute Cor Pulmonale 33 3.328
20
P ACT080 Acute Pulmonary Heart Disease 31 3.328
21
BTT011 Butterfly-Shaped Pigment Dystrophy 24 3.328
22
PLV004 Pelvic Varices 23 3.328
23
LRY011 Larynx Verrucous Carcinoma 22 3.328
24
P RNL014 Renal Cell Carcinoma 82 0.129
25
c HMP029 Hemophilia a 63 0.091
26
GLN010 Glanzmann Thrombasthenia 63 0.091
27
VNW001 Von Willebrand's Disease 61 0.091
28
P THR015 Thrombophilia 59 0.091
29
P HMP007 Hemophilia 57 0.091
30
P HMR003 Hemorrhagic Disease 57 0.091
31
c THR092 Thrombophilia Due to Thrombin Defect 54 0.091
32
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.091
33
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.091
34
ATR060 Atrial Standstill, Digenic 51 0.091
35
VNW005 Von Willebrand Disease, Type 1 49 0.091
36
HMR002 Hemarthrosis 48 0.091
37
P AFB001 Afibrinogenemia 48 0.091
38
LYM008 Lymphangiosarcoma 47 0.091
39
BLD053 Blood Platelet Disease 46 0.091
40
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.091
41
P BLD051 Blood Coagulation Disease 42 0.091
42
ACQ017 Acquired Von Willebrand Syndrome 37 0.091
43
c INH004 Inherited Blood Coagulation Disease 36 0.091
44
INT078 Intracranial Thrombosis 36 0.091
45
FNT004 Fainting 33 0.091
46
TYP015 Type 2b Von Willebrand Disease 30 0.091
47
P MLD013 Mild Hemophilia a 29 0.091
48
TYP017 Type 2n Von Willebrand Disease 19 0.091
49
TYP016 Type 2m Von Willebrand Disease 18 0.091
50
STR067 Stroke, Ischemic 75 0.064
51
P ESS003 Essential Thrombocythemia 70 0.064
52
P CNJ013 Conjunctivitis 64 0.064
53
P THR014 Thrombocytopenia 64 0.064
54
c ACT075 Acute Myocardial Infarction 60 0.064
55
PRP030 Purpura 58 0.064
56
THR024 Thrombosis 57 0.064
57
INT002 Intermittent Claudication 56 0.064
58
P ANT006 Antiphospholipid Syndrome 56 0.064
59
VRL011 Viral Infectious Disease 55 0.064
60
GRY002 Gray Platelet Syndrome 55 0.064
61
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.064
62
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.064
63
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.064
64
P VNS003 Venous Insufficiency 54 0.064
65
CYT008 Cytomegalovirus Infection 52 0.064
66
P HML001 Hemolytic-Uremic Syndrome 51 0.064
67
INT007 Intermediate Coronary Syndrome 50 0.064
68
CLF001 Cleft Lip 50 0.064
69
BRN082 Bernard-Soulier Syndrome, Type C 50 0.064
70
HLL004 Hellp Syndrome 50 0.064
71
CRN017 Coronary Thrombosis 48 0.064
72
HST009 Histiocytoma 47 0.064
73
c PRM225 Primary Thrombocytopenia 39 0.064
74
ATM012 Autoimmune Disease of Blood 35 0.064
75
QLT001 Qualitative Platelet Defect 32 0.064
76
VNW004 Von Willebrand Disease, Platelet-Type 31 0.064
77
CYT004 Cytomegalic Inclusion Disease 31 0.064
Content
Loading form....