Search results for f8

76 hits were found for f8

# Family MCID Name MIFTS Score
1
c HMP029 Hemophilia a 63 7.793
2
P HMP007 Hemophilia 57 4.252
3
P ART023 Arthropathy 64 3.258
4
c HMP004 Hemophilia B 62 3.233
5
VNW001 Von Willebrand's Disease 61 3.233
6
P THR015 Thrombophilia 59 3.206
7
P HMR003 Hemorrhagic Disease 57 3.206
8
HMR002 Hemarthrosis 48 3.206
9
BLD053 Blood Platelet Disease 46 3.206
10
CRD001 Cardiac Tamponade 44 3.206
11
c SVR056 Severe Hemophilia a 43 3.036
12
P MLD013 Mild Hemophilia a 29 2.950
13
P MDR007 Moderately Severe Hemophilia a 16 2.898
14
P MYC007 Myocardial Infarction 79 2.868
15
GLN010 Glanzmann Thrombasthenia 63 2.868
16
FCT007 Factor Vii Deficiency 61 2.868
17
FCT006 Factor V Deficiency 57 2.868
18
c THR092 Thrombophilia Due to Thrombin Defect 54 2.868
19
THR016 Thrombophlebitis 53 2.868
20
P CMP008 Compartment Syndrome 48 2.868
21
PST095 Post-Thrombotic Syndrome 47 2.868
22
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 2.868
23
VNW005 Von Willebrand Disease, Type 1 49 2.575
24
c ACQ014 Acquired Hemophilia 42 2.518
25
c ACQ042 Acquired Hemophilia a 40 2.518
26
P SYM020 Symptomatic Form of Hemophilia a in Female Carriers 4 2.518
27
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 2.484
28
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 2.484
29
HPT046 Hepatic Veno-Occlusive Disease 50 2.484
30
P AFB001 Afibrinogenemia 48 2.484
31
LYM008 Lymphangiosarcoma 47 2.484
32
VND001 Vein Disease 47 2.484
33
MLT113 Multicentric Castleman Disease 46 2.484
34
P RTN014 Retinal Artery Occlusion 44 2.484
35
CRT015 Carotid Artery Occlusion 43 2.484
36
FCT005 Factor Xiii Deficiency 43 2.484
37
MNN006 Meninges Hemangiopericytoma 42 2.484
38
NDL003 Nodular Nonsuppurative Panniculitis 42 2.484
39
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 2.484
40
P BLD051 Blood Coagulation Disease 42 2.484
41
TST018 Testicular Yolk Sac Tumor 40 2.484
42
BRS090 Breast Reconstruction 38 2.484
43
LNG013 Lung Lymphoma 38 2.484
44
ACQ017 Acquired Von Willebrand Syndrome 37 2.484
45
c INH004 Inherited Blood Coagulation Disease 36 2.484
46
INT078 Intracranial Thrombosis 36 2.484
47
SPL011 Spleen Cancer 36 2.484
48
c ACQ005 Acquired Thrombocytopenia 35 2.484
49
FRN014 Fournier Gangrene 35 2.484
50
FNT004 Fainting 33 2.484
51
FCT016 Factor V and Factor Viii, Combined Deficiency of 33 2.484
52
MCR001 Microcystic Meningioma 33 2.484
53
IND004 Indeterminate Leprosy 32 2.484
54
c SVR057 Severe Hemophilia B 32 2.484
55
TYP015 Type 2b Von Willebrand Disease 30 2.484
56
PRC014 Pericardium Cancer 30 2.484
57
THY001 Thyroid Crisis 27 2.484
58
INT083 Intraventricular Meningioma 26 2.484
59
PDT004 Pediatric Angiosarcoma 24 2.484
60
TBR007 Tuberculum Sellae Meningioma 24 2.484
61
TYP017 Type 2n Von Willebrand Disease 19 2.484
62
TYP016 Type 2m Von Willebrand Disease 18 2.484
63
HBN001 Hobnail Hemangioma 18 2.484
64
SLL002 Sella Turcica Neoplasm 17 2.484
65
P HYP620 Hypoprothrombinemia 54 2.028
66
IMM136 Immune System Disease 51 2.028
67
c DFN189 Deafness, Autosomal Dominant 25 33 2.028
68
ALC001 Alcohol-Related Birth Defect 31 2.028
69
CLR063 Colorblindness, Deutan 31 2.028
70
RDG001 Red-Green Color Blindness 30 2.028
71
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 42 0.110
72
THR024 Thrombosis 57 0.090
73
VNW003 Von Willibrand Disease, Type 3 30 0.090
74
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.064
75
P PSR002 Psoriasis 61 0.064
76
HMP018 Hemophilic Arthropathy 34 0.064
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