Search results for f8

77 hits were found for f8

# Family MCID Name MIFTS Score
1
c HMP029 Hemophilia a 64 7.784
2
P HMP007 Hemophilia 55 4.255
3
P ART023 Arthropathy 62 2.920
4
c HMP004 Hemophilia B 62 2.892
5
VNW001 Von Willebrand's Disease 60 2.892
6
P THR015 Thrombophilia 58 2.862
7
HMR002 Hemarthrosis 47 2.862
8
BLD053 Blood Platelet Disease 46 2.862
9
CRD001 Cardiac Tamponade 43 2.862
10
c SVR056 Severe Hemophilia a 43 2.661
11
P MLD013 Mild Hemophilia a 29 2.570
12
P MDR007 Moderately Severe Hemophilia a 16 2.513
13
P MYC007 Myocardial Infarction 77 2.479
14
GLN010 Glanzmann Thrombasthenia 64 2.479
15
FCT007 Factor Vii Deficiency 59 2.479
16
FCT006 Factor V Deficiency 59 2.479
17
P HMR003 Hemorrhagic Disease 55 2.479
18
THR016 Thrombophlebitis 52 2.479
19
c THR092 Thrombophilia Due to Thrombin Defect 50 2.479
20
PST095 Post-Thrombotic Syndrome 48 2.479
21
P CMP008 Compartment Syndrome 44 2.479
22
INT078 Intracranial Thrombosis 37 2.479
23
VTM001 Vitamin K Deficiency Hemorrhagic Disease 31 2.479
24
VNW005 Von Willebrand Disease, Type 1 47 2.099
25
c ACQ014 Acquired Hemophilia 40 2.064
26
c ACQ042 Acquired Hemophilia a 39 2.064
27
P HYP620 Hypoprothrombinemia 56 2.024
28
c AFB002 Afibrinogenemia, Congenital 52 2.024
29
BRN082 Bernard-Soulier Syndrome, Type C 52 2.024
30
c THR082 Thrombophilia Due to Activated Protein C Resistance 51 2.024
31
VND001 Vein Disease 49 2.024
32
LYM008 Lymphangiosarcoma 46 2.024
33
P AFB001 Afibrinogenemia 46 2.024
34
FCT005 Factor Xiii Deficiency 46 2.024
35
MLT113 Multicentric Castleman Disease 45 2.024
36
FCT022 Factor Xi Deficiency, Autosomal Recessive 44 2.024
37
P BLD051 Blood Coagulation Disease 43 2.024
38
NDL003 Nodular Nonsuppurative Panniculitis 43 2.024
39
MNN006 Meninges Hemangiopericytoma 42 2.024
40
P RTN014 Retinal Artery Occlusion 42 2.024
41
CRT015 Carotid Artery Occlusion 41 2.024
42
TST018 Testicular Yolk Sac Tumor 41 2.024
43
LNG013 Lung Lymphoma 40 2.024
44
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 39 2.024
45
c INH004 Inherited Blood Coagulation Disease 39 2.024
46
BRS090 Breast Reconstruction 38 2.024
47
SPL011 Spleen Cancer 37 2.024
48
ACQ017 Acquired Von Willebrand Syndrome 36 2.024
49
c ACQ005 Acquired Thrombocytopenia 36 2.024
50
FRN014 Fournier Gangrene 34 2.024
51
P XLN007 X-Linked Disease 34 2.024
52
c DFN189 Deafness, Autosomal Dominant 25 33 2.024
53
FCT016 Factor V and Factor Viii, Combined Deficiency of 33 2.024
54
MCR001 Microcystic Meningioma 33 2.024
55
FNT004 Fainting 33 2.024
56
IND004 Indeterminate Leprosy 33 2.024
57
c SVR057 Severe Hemophilia B 31 2.024
58
PRC014 Pericardium Cancer 31 2.024
59
ALC001 Alcohol-Related Birth Defect 30 2.024
60
TYP015 Type 2b Von Willebrand Disease 30 2.024
61
RDG001 Red-Green Color Blindness 30 2.024
62
THY001 Thyroid Crisis 27 2.024
63
INT083 Intraventricular Meningioma 26 2.024
64
PDT004 Pediatric Angiosarcoma 25 2.024
65
TBR007 Tuberculum Sellae Meningioma 24 2.024
66
SLL002 Sella Turcica Neoplasm 21 2.024
67
TYP017 Type 2n Von Willebrand Disease 18 2.024
68
HBN001 Hobnail Hemangioma 18 2.024
69
TYP016 Type 2m Von Willebrand Disease 18 2.024
70
P SYM020 Symptomatic Form of Hemophilia a in Female Carriers 7 1.484
71
IMM136 Immune System Disease 53 1.431
72
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 35 0.110
73
THR024 Thrombosis 43 0.090
74
VNW003 Von Willibrand Disease, Type 3 24 0.090
75
P PSR002 Psoriasis 64 0.064
76
PNC041 Pancreatic Ductal Adenocarcinoma 62 0.064
77
HMP018 Hemophilic Arthropathy 33 0.064
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