Search results for f8

77 hits were found for f8

# Family MCID Name MIFTS Score
1
c HMP029 Hemophilia a 69 7.422
2
P HMP007 Hemophilia 61 4.291
3
FCT001 Factor Viii Deficiency 50 2.995
4
P ART023 Arthropathy 68 2.925
5
c HMP004 Hemophilia B 67 2.898
6
VNW001 Von Willebrand's Disease 61 2.898
7
P HMR003 Hemorrhagic Disease 61 2.868
8
P THR015 Thrombophilia 58 2.868
9
HMR002 Hemarthrosis 51 2.868
10
BLD053 Blood Platelet Disease 45 2.868
11
CRD001 Cardiac Tamponade 45 2.868
12
c SVR056 Severe Hemophilia a 46 2.665
13
P MLD013 Mild Hemophilia a 30 2.600
14
c THR092 Thrombophilia Due to Thrombin Defect 61 2.548
15
P MDR007 Moderately Severe Hemophilia a 16 2.518
16
P MYC007 Myocardial Infarction 81 2.484
17
GLN010 Glanzmann Thrombasthenia 66 2.484
18
FCT007 Factor Vii Deficiency 62 2.484
19
P BRN019 Bernard-Soulier Syndrome 60 2.484
20
THR016 Thrombophlebitis 53 2.484
21
PST095 Post-Thrombotic Syndrome 52 2.484
22
FCT006 Factor V Deficiency 52 2.484
23
P CMP008 Compartment Syndrome 48 2.484
24
INT078 Intracranial Thrombosis 37 2.484
25
VTM001 Vitamin K Deficiency Hemorrhagic Disease 35 2.484
26
VNW010 Von Willebrand Disease, Type 2 45 2.132
27
VNW005 Von Willebrand Disease, Type 1 47 2.102
28
VNW008 Von Willebrand Disease, Type 3 43 2.102
29
c ACQ014 Acquired Hemophilia 51 2.068
30
c ACQ042 Acquired Hemophilia a 44 2.068
31
FCT002 Factor Xi Deficiency 64 2.028
32
c AFB002 Afibrinogenemia, Congenital 61 2.028
33
LYM008 Lymphangiosarcoma 51 2.028
34
MLT113 Multicentric Castleman Disease 49 2.028
35
P AFB001 Afibrinogenemia 49 2.028
36
VND001 Vein Disease 48 2.028
37
NDL003 Nodular Nonsuppurative Panniculitis 47 2.028
38
c THR082 Thrombophilia Due to Activated Protein C Resistance 47 2.028
39
FCT005 Factor Xiii Deficiency 46 2.028
40
PRT012 Prothrombin Deficiency 46 2.028
41
P RTN014 Retinal Artery Occlusion 45 2.028
42
TST018 Testicular Yolk Sac Tumor 44 2.028
43
CRT015 Carotid Artery Occlusion 42 2.028
44
BRS090 Breast Reconstruction 41 2.028
45
ACQ017 Acquired Von Willebrand Syndrome 40 2.028
46
MNN006 Meninges Hemangiopericytoma 39 2.028
47
FRN014 Fournier Gangrene 38 2.028
48
P BLD051 Blood Coagulation Disease 38 2.028
49
MCR001 Microcystic Meningioma 36 2.028
50
FNT004 Fainting 36 2.028
51
FCT034 Factor V and Factor Viii, Combined Deficiency of, 2 35 2.028
52
c DFN189 Deafness, Autosomal Dominant 25 34 2.028
53
LNG013 Lung Lymphoma 34 2.028
54
c SVR057 Severe Hemophilia B 32 2.028
55
IND004 Indeterminate Leprosy 32 2.028
56
ALC001 Alcohol-Related Birth Defect 32 2.028
57
RDG001 Red-Green Color Blindness 30 2.028
58
SPL011 Spleen Cancer 30 2.028
59
THY001 Thyroid Crisis 30 2.028
60
c INH004 Inherited Blood Coagulation Disease 29 2.028
61
CRB005 Cerebral Arteritis 28 2.028
62
TBR007 Tuberculum Sellae Meningioma 28 2.028
63
PRC014 Pericardium Cancer 28 2.028
64
P XLN007 X-Linked Disease 28 2.028
65
PDT004 Pediatric Angiosarcoma 27 2.028
66
INT083 Intraventricular Meningioma 26 2.028
67
SLL002 Sella Turcica Neoplasm 23 2.028
68
HBN001 Hobnail Hemangioma 20 2.028
69
P SYM020 Symptomatic Form of Hemophilia a in Female Carriers 4 1.487
70
IMM136 Immune System Disease 57 1.434
71
THR024 Thrombosis 61 0.090
72
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.090
73
c BLD140 Blood Group, I System 37 0.090
74
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.064
75
P PSR002 Psoriasis 65 0.064
76
PST011 Pustulosis of Palm and Sole 47 0.064
77
HMP018 Hemophilic Arthropathy 37 0.064
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