Search results for f5

122 hits were found for f5

# Family MCID Name MIFTS Score
1
FCT006 Factor V Deficiency 59 4.736
2
c THR082 Thrombophilia Due to Activated Protein C Resistance 51 4.307
3
P BDD001 Budd-Chiari Syndrome 56 3.996
4
STR067 Stroke, Ischemic 72 3.543
5
P THR015 Thrombophilia 58 3.452
6
PRG092 Pregnancy Loss, Recurrent 1 31 3.275
7
PRT011 Protein C Deficiency 49 2.917
8
THR024 Thrombosis 43 2.659
9
c HMP029 Hemophilia a 64 2.609
10
PLM033 Pulmonary Embolism 59 2.609
11
P ANT006 Antiphospholipid Syndrome 54 2.609
12
PRT014 Protein S Deficiency 51 2.609
13
P HMC002 Homocystinuria 49 2.609
14
HYP037 Hyperhomocysteinemia 49 2.609
15
PST095 Post-Thrombotic Syndrome 48 2.609
16
HLL004 Hellp Syndrome 48 2.609
17
PRT018 Portal Vein Thrombosis 47 2.609
18
PLC007 Placental Abruption 46 2.609
19
VND001 Vein Disease 49 2.316
20
VSC007 Vascular Disease 65 2.290
21
CRB132 Cerebral Sinovenous Thrombosis 29 2.290
22
P MYC007 Myocardial Infarction 77 2.260
23
OVR029 Ovarian Hyperstimulation Syndrome 61 2.260
24
VNW001 Von Willebrand's Disease 60 2.260
25
P PLY018 Polycythemia 56 2.260
26
c ACT210 Acute Respiratory Distress Syndrome 56 2.260
27
LGG001 Legg-Calve-Perthes Disease 56 2.260
28
P HYP620 Hypoprothrombinemia 56 2.260
29
P HMR003 Hemorrhagic Disease 55 2.260
30
PTN001 Patent Foramen Ovale 54 2.260
31
CRB037 Cerebral Palsy 54 2.260
32
THR016 Thrombophlebitis 52 2.260
33
c THR092 Thrombophilia Due to Thrombin Defect 50 2.260
34
DSS009 Disseminated Intravascular Coagulation 50 2.260
35
FCT004 Factor Xii Deficiency 50 2.260
36
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 48 2.260
37
c ACT134 Acute Liver Failure 48 2.260
38
c SVR005 Severe Pre-Eclampsia 48 2.260
39
P DYS026 Dysfibrinogenemia 47 2.260
40
FCT005 Factor Xiii Deficiency 46 2.260
41
RTN021 Retinal Vascular Occlusion 45 2.260
42
CRT015 Carotid Artery Occlusion 41 2.260
43
P RTN022 Retinal Vein Occlusion 37 2.260
44
INT078 Intracranial Thrombosis 37 2.260
45
c CNT016 Central Retinal Vein Occlusion 35 2.260
46
HMC014 Homocysteinemia 34 2.260
47
PLC008 Placenta Disease 32 2.260
48
THR035 Thrombasthenia 41 1.880
49
BLD054 Blood Protein Disease 39 1.880
50
CRB039 Cerebrovascular Disease 63 1.845
51
FCT003 Factor X Deficiency 59 1.845
52
P PRC031 Preeclampsia/eclampsia 1 55 1.845
53
P SCH018 Schizencephaly 52 1.845
54
QBC001 Quebec Platelet Disorder 52 1.845
55
SCT005 Scott Syndrome 51 1.845
56
P ECL001 Eclampsia 51 1.845
57
INT075 Intracranial Hypertension 48 1.845
58
SND002 Sneddon Syndrome 48 1.845
59
P PRN026 Porencephaly 48 1.845
60
P AFB001 Afibrinogenemia 46 1.845
61
PRP007 Priapism 45 1.845
62
FCT022 Factor Xi Deficiency, Autosomal Recessive 44 1.845
63
ISC002 Ischemic Optic Neuropathy 44 1.845
64
SPS007 Spastic Cerebral Palsy 43 1.845
65
EBL001 Ebola Hemorrhagic Fever 43 1.845
66
c HMG003 Hemoglobin E Disease 43 1.845
67
c SVR056 Severe Hemophilia a 43 1.845
68
c ACQ012 Acquired Angioedema 42 1.845
69
P RTN014 Retinal Artery Occlusion 42 1.845
70
CTS005 Catastrophic Antiphospholipid Syndrome 41 1.845
71
c ACQ014 Acquired Hemophilia 40 1.845
72
MDS022 Mediastinitis 40 1.845
73
c ACQ042 Acquired Hemophilia a 39 1.845
74
ALV006 Alveolar Capillary Dysplasia 38 1.845
75
MNN021 Meningococcemia 38 1.845
76
ISC015 Ischemic Colitis 38 1.845
77
PRP028 Peripheral Vertigo 38 1.845
78
AMR003 Amaurosis Fugax 37 1.845
79
ACN019 Acanthamoeba Keratitis 37 1.845
80
SPN185 Spinal Cord Infarction 33 1.845
81
FCT016 Factor V and Factor Viii, Combined Deficiency of 33 1.845
82
SGT001 Sagittal Sinus Thrombosis 33 1.845
83
LVD002 Livedoid Vasculopathy 32 1.845
84
SDD008 Sudden Sensorineural Hearing Loss 30 1.845
85
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 1.845
86
STC016 Sticky Platelet Syndrome 30 1.845
87
INF133 Inferior Vena Cava Interruption 29 1.845
88
PRC051 Paracetamol Poisoning 28 1.845
89
MYT019 May-Thurner Syndrome 24 1.845
90
MTH044 Mthfr Gene Mutation 23 1.845
91
FCT013 Factor V Leiden Thrombophilia 22 1.386
92
BLD072 Bleeding Disorder, East Texas Type 17 1.351
93
FCT017 Factor V Cambridge Thrombophilia 7 1.351
94
c F5R001 F5-Related Budd-Chiari Syndrome 5 1.351
95
FCT018 Factor V R2 Mutation Thrombophilia 4 1.351
96
BHC003 Behcet Syndrome 62 1.305
97
P BLD051 Blood Coagulation Disease 43 1.305
98
MLN008 Melanoma 70 0.096
99
ACQ007 Acquired Immunodeficiency Syndrome 60 0.096
100
NRN004 Neuroendocrine Tumor 55 0.096
101
c CLL013 Cell Type Cancer 48 0.096
102
GRM001 Germ Cell and Embryonal Cancer 38 0.096
103
P GRM010 Germ Cells Tumors 34 0.096
104
SKN019 Skin Melanoma 61 0.078
105
VRL011 Viral Infectious Disease 59 0.078
106
SKN023 Skin Tag 46 0.078
107
LKC003 Leukocyte Disease 46 0.078
108
P BRS047 Breast Cancer 100 0.055
109
P OBS005 Obesity 91 0.055
110
PCK002 Pick Disease 68 0.055
111
GLN010 Glanzmann Thrombasthenia 64 0.055
112
P NRV006 Nervous System Cancer 59 0.055
113
OCL009 Ocular Cancer 58 0.055
114
OCL022 Ocular Melanoma 50 0.055
115
PRP021 Peripheral Nervous System Neoplasm 48 0.055
116
P RNL017 Renal Oncocytoma 45 0.055
117
SNS023 Sensory System Cancer 44 0.055
118
MCS004 Mucosal Melanoma 41 0.055
119
GST009 Gastroschisis 40 0.055
120
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.055
121
MLN013 Melanoma Metastasis 38 0.055
122
MLG109 Malignant Melanoma of the Mucosa 12 0.055
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