Search results for f3

151 hits were found for f3

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 75 3.254
2
STR067 Stroke, Ischemic 75 2.719
3
PRP027 Peripheral Vascular Disease 68 2.719
4
P THR014 Thrombocytopenia 64 2.719
5
c HMP029 Hemophilia a 63 2.719
6
GLN010 Glanzmann Thrombasthenia 63 2.719
7
c HMP004 Hemophilia B 62 2.719
8
FCT003 Factor X Deficiency 61 2.719
9
VNW001 Von Willebrand's Disease 61 2.719
10
FCT007 Factor Vii Deficiency 61 2.719
11
c ACT075 Acute Myocardial Infarction 60 2.719
12
PLM033 Pulmonary Embolism 60 2.719
13
P THR015 Thrombophilia 59 2.719
14
P HMR003 Hemorrhagic Disease 57 2.719
15
P ANT006 Antiphospholipid Syndrome 56 2.719
16
THR004 Thrombocytosis 55 2.719
17
P MNC007 Monocytic Leukemia 55 2.719
18
PRT014 Protein S Deficiency 53 2.719
19
DSS009 Disseminated Intravascular Coagulation 51 2.719
20
FCT004 Factor Xii Deficiency 50 2.719
21
CRT004 Carotid Artery Thrombosis 40 2.719
22
c HPT003 Hepatitis a 59 2.457
23
THR024 Thrombosis 57 2.457
24
MLR004 Malaria 83 2.432
25
P PLM037 Pulmonary Hypertension 79 2.432
26
P MYC007 Myocardial Infarction 79 2.432
27
P RSP003 Respiratory Failure 71 2.432
28
VSC007 Vascular Disease 67 2.432
29
DNG002 Dengue Hemorrhagic Fever 63 2.432
30
c ATM010 Autoimmune Hemolytic Anemia 60 2.432
31
PRP030 Purpura 58 2.432
32
FCT006 Factor V Deficiency 57 2.432
33
P BDD001 Budd-Chiari Syndrome 56 2.432
34
P THR005 Thrombotic Thrombocytopenic Purpura 55 2.432
35
SCR008 Scrub Typhus 55 2.432
36
CRM001 Crimean-Congo Hemorrhagic Fever 55 2.432
37
c THR092 Thrombophilia Due to Thrombin Defect 54 2.432
38
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 2.432
39
c AFB002 Afibrinogenemia, Congenital 54 2.432
40
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 2.432
41
LKM067 Leukemia, Acute Promyelocytic, Somatic 52 2.432
42
HNT002 Hantavirus Pulmonary Syndrome 51 2.432
43
HPT046 Hepatic Veno-Occlusive Disease 50 2.432
44
INT075 Intracranial Hypertension 50 2.432
45
PLC005 Placental Insufficiency 50 2.432
46
HLL004 Hellp Syndrome 50 2.432
47
CRN017 Coronary Thrombosis 48 2.432
48
BLD053 Blood Platelet Disease 46 2.432
49
FCT005 Factor Xiii Deficiency 43 2.432
50
P PRP034 Purpura Fulminans 41 2.432
51
SGT001 Sagittal Sinus Thrombosis 35 2.432
52
PLC008 Placenta Disease 33 2.432
53
ART021 Arteriosclerosis 58 2.106
54
P HMP007 Hemophilia 57 2.106
55
P HMR012 Hemorrhagic Fever 56 2.106
56
ART111 Artery Disease 55 2.106
57
P HYP620 Hypoprothrombinemia 54 2.106
58
CFF003 Caffey Disease 54 2.106
59
IMM136 Immune System Disease 51 2.106
60
NDL013 Nodular Regenerative Hyperplasia 50 2.106
61
INT007 Intermediate Coronary Syndrome 50 2.106
62
ANG054 Angina Pectoris 50 2.106
63
VNW005 Von Willebrand Disease, Type 1 49 2.106
64
PYD002 Pyoderma 48 2.106
65
P AFB001 Afibrinogenemia 48 2.106
66
VND001 Vein Disease 47 2.106
67
SPL012 Splenic Disease 46 2.106
68
MLT113 Multicentric Castleman Disease 46 2.106
69
HPR003 Heparin-Induced Thrombocytopenia 45 2.106
70
P ANL018 Analbuminemia 44 2.106
71
c SVR056 Severe Hemophilia a 43 2.106
72
LMR001 Lemierre's Syndrome 43 2.106
73
c ACQ014 Acquired Hemophilia 42 2.106
74
HPT020 Hepatic Vascular Disease 42 2.106
75
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 2.106
76
CTS005 Catastrophic Antiphospholipid Syndrome 42 2.106
77
P BLD051 Blood Coagulation Disease 42 2.106
78
c ACQ042 Acquired Hemophilia a 40 2.106
79
SQM002 Squamous Cell Papilloma 40 2.106
80
LCH001 Leech Infestation 40 2.106
81
KRN001 Korean Hemorrhagic Fever 39 2.106
82
BRN026 Branch Retinal Artery Occlusion 38 2.106
83
VRT003 Vertebrobasilar Insufficiency 38 2.106
84
FMR003 Femoral Neuropathy 38 2.106
85
PRP028 Peripheral Vertigo 38 2.106
86
SHW001 Shwartzman Phenomenon 37 2.106
87
VRT001 Vertebral Artery Occlusion 36 2.106
88
c INH004 Inherited Blood Coagulation Disease 36 2.106
89
INT078 Intracranial Thrombosis 36 2.106
90
BLD009 Bladder Neck Obstruction 35 2.106
91
BLT003 Blue Toe Syndrome 35 2.106
92
GNT005 Giant Hemangioma 35 2.106
93
FRN014 Fournier Gangrene 35 2.106
94
PLM013 Pulmonary Immaturity 34 2.106
95
CHL010 Childhood Kidney Cell Carcinoma 33 2.106
96
MRN001 Marantic Endocarditis 32 2.106
97
DYS013 Dysbaric Osteonecrosis 32 2.106
98
QLT001 Qualitative Platelet Defect 32 2.106
99
INT050 Intestinal Impaction 31 2.106
100
CRB132 Cerebral Sinovenous Thrombosis 31 2.106
101
c ACT072 Acute Laryngitis 30 2.106
102
URT016 Urethral Diverticulum 30 2.106
103
CNJ001 Conjugate Gaze Palsy 29 2.106
104
ANT022 Anterior Cranial Fossa Meningioma 28 2.106
105
CNG016 Congenital Intrinsic Factor Deficiency 28 2.106
106
END074 Endocardium Disease 26 2.106
107
INT076 Intracranial Sinus Thrombosis 24 2.106
108
MXD019 Mixed Malaria 23 2.106
109
WHT003 White Piedra 22 2.106
110
BNP002 Bone Epithelioid Hemangioma 21 2.106
111
CRB017 Cerebral Falx Meningioma 21 2.106
112
PRT006 Partial Motor Epilepsy 20 2.106
113
BLV001 Bolivian Hemorrhagic Fever 18 2.106
114
HMM001 Hemometra 17 2.106
115
CHR051 Chorea Gravidarum 15 2.106
116
SNL011 Snail Allergy 12 2.106
117
c LKM061 Leukemia, Acute Myeloid 73 1.720
118
INT088 Intrinsic Factor Deficiency 45 1.720
119
c RTN177 Retinitis Pigmentosa 73 35 1.720
120
HPT081 Hepatic Infarction 34 1.720
121
ALC001 Alcohol-Related Birth Defect 31 1.720
122
SRC011 Sarcocystosis 29 1.720
123
NRN002 Neuronitis 41 0.147
124
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.073
125
P PRS040 Prostate Cancer 90 0.052
126
P HNT016 Huntington Disease 80 0.052
127
c HPT073 Hepatitis C Virus 73 0.052
128
P HPT021 Hepatitis 69 0.052
129
c HPT001 Hepatitis C 68 0.052
130
LVR012 Liver Cirrhosis 67 0.052
131
c HPT016 Hepatitis B 64 0.052
132
P THL005 Thalassemia 64 0.052
133
P ASP006 Aspergillosis 61 0.052
134
PRM097 Primary Immunodeficiency Disease 60 0.052
135
c VRL010 Viral Hepatitis 60 0.052
136
FTT001 Fatty Liver Disease 59 0.052
137
ADM013 Adamantinoma of Long Bones 57 0.052
138
P PLY019 Polyneuropathy 56 0.052
139
PRS047 Prostatitis 56 0.052
140
GST050 Gastrointestinal System Disease 56 0.052
141
VRL011 Viral Infectious Disease 55 0.052
142
P SPS003 Spastic Diplegia 52 0.052
143
DBT004 Diabetic Polyneuropathy 52 0.052
144
STM006 Stomach Disease 50 0.052
145
NNL002 Nonalcoholic Steatohepatitis 50 0.052
146
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.052
147
VSC018 Visceral Steatosis 37 0.052
148
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.052
149
IMM076 Immunodeficiency 24 27 0.052
150
IMM071 Immunodeficiency 12 26 0.052
151
IMM142 Immunodeficiency 50 20 0.052
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