Search results for f3

149 hits were found for f3

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 72 2.769
2
c SYS001 Systemic Lupus Erythematosus 86 2.439
3
STR067 Stroke, Ischemic 72 2.439
4
PRP027 Peripheral Vascular Disease 65 2.439
5
c HMP029 Hemophilia a 64 2.439
6
GLN010 Glanzmann Thrombasthenia 64 2.439
7
c HMP004 Hemophilia B 62 2.439
8
VNW001 Von Willebrand's Disease 60 2.439
9
c ACT075 Acute Myocardial Infarction 59 2.439
10
FCT007 Factor Vii Deficiency 59 2.439
11
PLM033 Pulmonary Embolism 59 2.439
12
FCT003 Factor X Deficiency 59 2.439
13
P THR015 Thrombophilia 58 2.439
14
P ANT006 Antiphospholipid Syndrome 54 2.439
15
P MNC007 Monocytic Leukemia 54 2.439
16
THR004 Thrombocytosis 52 2.439
17
PRT014 Protein S Deficiency 51 2.439
18
DSS009 Disseminated Intravascular Coagulation 50 2.439
19
FCT004 Factor Xii Deficiency 50 2.439
20
CRT004 Carotid Artery Thrombosis 40 2.439
21
c HPT003 Hepatitis a 56 2.140
22
THR024 Thrombosis 43 2.140
23
MLR004 Malaria 82 2.112
24
P MYC007 Myocardial Infarction 77 2.112
25
P PLM037 Pulmonary Hypertension 77 2.112
26
P HRT032 Heart Disease 75 2.112
27
VSC007 Vascular Disease 65 2.112
28
P THR014 Thrombocytopenia 63 2.112
29
c ATM010 Autoimmune Hemolytic Anemia 60 2.112
30
DNG002 Dengue Hemorrhagic Fever 60 2.112
31
SCR008 Scrub Typhus 59 2.112
32
FCT006 Factor V Deficiency 59 2.112
33
PRP030 Purpura 57 2.112
34
P THR005 Thrombotic Thrombocytopenic Purpura 57 2.112
35
P BDD001 Budd-Chiari Syndrome 56 2.112
36
P HMR003 Hemorrhagic Disease 55 2.112
37
CRM001 Crimean-Congo Hemorrhagic Fever 55 2.112
38
PLC005 Placental Insufficiency 53 2.112
39
c THR082 Thrombophilia Due to Activated Protein C Resistance 51 2.112
40
c THR092 Thrombophilia Due to Thrombin Defect 50 2.112
41
HPT046 Hepatic Veno-Occlusive Disease 50 2.112
42
HLL004 Hellp Syndrome 48 2.112
43
INT075 Intracranial Hypertension 48 2.112
44
HNT002 Hantavirus Pulmonary Syndrome 47 2.112
45
CRN017 Coronary Thrombosis 47 2.112
46
LKM067 Leukemia, Acute Promyelocytic, Somatic 47 2.112
47
FCT005 Factor Xiii Deficiency 46 2.112
48
BLD053 Blood Platelet Disease 46 2.112
49
FCT022 Factor Xi Deficiency, Autosomal Recessive 44 2.112
50
P PRP034 Purpura Fulminans 40 2.112
51
INT078 Intracranial Thrombosis 37 2.112
52
SGT001 Sagittal Sinus Thrombosis 33 2.112
53
PLC008 Placenta Disease 32 2.112
54
P ESS003 Essential Thrombocythemia 70 1.724
55
P RSP003 Respiratory Failure 68 1.724
56
ART021 Arteriosclerosis 57 1.724
57
P HYP620 Hypoprothrombinemia 56 1.724
58
ART111 Artery Disease 55 1.724
59
P HMP007 Hemophilia 55 1.724
60
CFF003 Caffey Disease 55 1.724
61
IMM136 Immune System Disease 53 1.724
62
c AFB002 Afibrinogenemia, Congenital 52 1.724
63
P HMR012 Hemorrhagic Fever 52 1.724
64
INT007 Intermediate Coronary Syndrome 50 1.724
65
ANG054 Angina Pectoris 49 1.724
66
VND001 Vein Disease 49 1.724
67
VNW005 Von Willebrand Disease, Type 1 47 1.724
68
NDL013 Nodular Regenerative Hyperplasia 47 1.724
69
P AFB001 Afibrinogenemia 46 1.724
70
SPL012 Splenic Disease 46 1.724
71
MLT113 Multicentric Castleman Disease 45 1.724
72
HPR003 Heparin-Induced Thrombocytopenia 44 1.724
73
P BLD051 Blood Coagulation Disease 43 1.724
74
LMR001 Lemierre's Syndrome 43 1.724
75
c SVR056 Severe Hemophilia a 43 1.724
76
HPT020 Hepatic Vascular Disease 42 1.724
77
THR035 Thrombasthenia 41 1.724
78
CTS005 Catastrophic Antiphospholipid Syndrome 41 1.724
79
SQM002 Squamous Cell Papilloma 40 1.724
80
c ACQ014 Acquired Hemophilia 40 1.724
81
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 39 1.724
82
LCH001 Leech Infestation 39 1.724
83
c INH004 Inherited Blood Coagulation Disease 39 1.724
84
P ANL018 Analbuminemia 39 1.724
85
c ACQ042 Acquired Hemophilia a 39 1.724
86
c RTN177 Retinitis Pigmentosa 73 38 1.724
87
VRT003 Vertebrobasilar Insufficiency 38 1.724
88
PRP028 Peripheral Vertigo 38 1.724
89
SHW001 Shwartzman Phenomenon 37 1.724
90
FMR003 Femoral Neuropathy 37 1.724
91
PLM013 Pulmonary Immaturity 37 1.724
92
BLD009 Bladder Neck Obstruction 36 1.724
93
HPT081 Hepatic Infarction 35 1.724
94
BLT003 Blue Toe Syndrome 35 1.724
95
VRT001 Vertebral Artery Occlusion 34 1.724
96
FRN014 Fournier Gangrene 34 1.724
97
GNT005 Giant Hemangioma 34 1.724
98
BRN026 Branch Retinal Artery Occlusion 34 1.724
99
KRN001 Korean Hemorrhagic Fever 34 1.724
100
CHL010 Childhood Kidney Cell Carcinoma 33 1.724
101
MRN001 Marantic Endocarditis 33 1.724
102
DYS013 Dysbaric Osteonecrosis 31 1.724
103
ALC001 Alcohol-Related Birth Defect 30 1.724
104
INT050 Intestinal Impaction 30 1.724
105
c ACT072 Acute Laryngitis 30 1.724
106
URT016 Urethral Diverticulum 29 1.724
107
CRB132 Cerebral Sinovenous Thrombosis 29 1.724
108
CNJ001 Conjugate Gaze Palsy 28 1.724
109
END074 Endocardium Disease 28 1.724
110
ANT022 Anterior Cranial Fossa Meningioma 28 1.724
111
CNG016 Congenital Intrinsic Factor Deficiency 28 1.724
112
INT076 Intracranial Sinus Thrombosis 24 1.724
113
MXD019 Mixed Malaria 22 1.724
114
WHT003 White Piedra 21 1.724
115
CRB017 Cerebral Falx Meningioma 21 1.724
116
PRT006 Partial Motor Epilepsy 20 1.724
117
BNP002 Bone Epithelioid Hemangioma 18 1.724
118
HMM001 Hemometra 17 1.724
119
BLV001 Bolivian Hemorrhagic Fever 15 1.724
120
CHR051 Chorea Gravidarum 14 1.724
121
SNL011 Snail Allergy 12 1.724
122
c LKM061 Leukemia, Acute Myeloid 74 1.219
123
NRN002 Neuronitis 39 0.148
124
P PRS040 Prostate Cancer 88 0.052
125
c HPT073 Hepatitis C Virus 70 0.052
126
P HPT021 Hepatitis 68 0.052
127
LVR012 Liver Cirrhosis 66 0.052
128
c HPT001 Hepatitis C 62 0.052
129
c HPT016 Hepatitis B 62 0.052
130
P THL005 Thalassemia 61 0.052
131
P ASP006 Aspergillosis 60 0.052
132
ACQ007 Acquired Immunodeficiency Syndrome 60 0.052
133
VRL011 Viral Infectious Disease 59 0.052
134
FTT001 Fatty Liver Disease 59 0.052
135
c VRL010 Viral Hepatitis 58 0.052
136
P GT001 Gout 55 0.052
137
PRS047 Prostatitis 55 0.052
138
P PLY019 Polyneuropathy 54 0.052
139
GST050 Gastrointestinal System Disease 53 0.052
140
P SPS003 Spastic Diplegia 52 0.052
141
NWC001 Newcastle Disease 51 0.052
142
NNL002 Nonalcoholic Steatohepatitis 50 0.052
143
DBT004 Diabetic Polyneuropathy 47 0.052
144
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.052
145
VSC018 Visceral Steatosis 41 0.052
146
P FTT008 Fatty Liver Disease, Nonalcoholic 1 31 0.052
147
IMM071 Immunodeficiency 12 30 0.052
148
IMM076 Immunodeficiency 24 29 0.052
149
IMM142 Immunodeficiency 50 24 0.052
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