Search results for F3

181 hits were found for F3

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 71 2.554
2
STR067 Stroke, Ischemic 82 2.489
3
GLN010 Glanzmann Thrombasthenia 66 2.489
4
c HMP004 Hemophilia B 66 2.489
5
FCT007 Factor Vii Deficiency 65 2.489
6
P VNW001 Von Willebrand's Disease 64 2.489
7
ACT119 Acute Promyelocytic Leukemia 63 2.489
8
PLM033 Pulmonary Embolism 60 2.489
9
FCT002 Factor Xi Deficiency 59 2.489
10
P THR005 Thrombotic Thrombocytopenic Purpura 59 2.489
11
c ACT075 Acute Myocardial Infarction 59 2.489
12
DSS009 Disseminated Intravascular Coagulation 58 2.489
13
THR024 Thrombosis 58 2.489
14
FCT003 Factor X Deficiency 57 2.489
15
P ANT006 Antiphospholipid Syndrome 56 2.489
16
FCT004 Factor Xii Deficiency 54 2.489
17
P HMR003 Hemorrhagic Disease 54 2.489
18
P MNC007 Monocytic Leukemia 52 2.489
19
THR004 Thrombocytosis 52 2.489
20
P THR015 Thrombophilia 51 2.489
21
PRT014 Protein S Deficiency 50 2.489
22
CRT004 Carotid Artery Thrombosis 37 2.489
23
LVR012 Liver Cirrhosis 67 2.248
24
c HPT003 Hepatitis a 60 2.207
25
c THR092 Thrombophilia Due to Thrombin Defect 74 2.183
26
P VSC007 Vascular Disease 65 2.183
27
c SYS001 Systemic Lupus Erythematosus 88 2.156
28
MLR004 Malaria 82 2.156
29
P HRT032 Heart Disease 78 2.156
30
P MYC007 Myocardial Infarction 74 2.156
31
PRP027 Peripheral Vascular Disease 72 2.156
32
c HMP029 Hemophilia a 69 2.156
33
P THR014 Thrombocytopenia 67 2.156
34
c PRC016 Pre-Eclampsia 63 2.156
35
BDD001 Budd-Chiari Syndrome 62 2.156
36
c AFB002 Afibrinogenemia, Congenital 62 2.156
37
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 2.156
38
DNG002 Dengue Hemorrhagic Fever 59 2.156
39
PRP030 Purpura 56 2.156
40
SCR008 Scrub Typhus 56 2.156
41
HPT046 Hepatic Veno-Occlusive Disease 56 2.156
42
PLC005 Placental Insufficiency 55 2.156
43
INT075 Intracranial Hypertension 54 2.156
44
P HML001 Hemolytic-Uremic Syndrome 54 2.156
45
HLL004 Hellp Syndrome 53 2.156
46
FCT006 Factor V Deficiency 53 2.156
47
PLC008 Placenta Disease 51 2.156
48
BLD053 Blood Platelet Disease 51 2.156
49
FCT005 Factor Xiii Deficiency 50 2.156
50
CRM001 Crimean-Congo Hemorrhagic Fever 49 2.156
51
c VNW005 Von Willebrand Disease, Type 1 49 2.156
52
HNT002 Hantavirus Pulmonary Syndrome 48 2.156
53
INT078 Intracranial Thrombosis 48 2.156
54
CRN017 Coronary Thrombosis 45 2.156
55
P PRP034 Purpura Fulminans 42 2.156
56
SGT001 Sagittal Sinus Thrombosis 33 2.156
57
c HYP595 Hypertension, Essential 87 1.760
58
P RSP003 Respiratory Failure 75 1.760
59
P ESS003 Essential Thrombocythemia 69 1.760
60
BRS051 Breast Disease 59 1.760
61
c VNW010 Von Willebrand Disease, Type 2 58 1.760
62
P HMP007 Hemophilia 58 1.760
63
INT007 Intermediate Coronary Syndrome 58 1.760
64
P ART021 Arteriosclerosis 56 1.760
65
GRN034 Grange Syndrome 55 1.760
66
CFF003 Caffey Disease 54 1.760
67
P ANL018 Analbuminemia 51 1.760
68
c VNW008 Von Willebrand Disease, Type 3 49 1.760
69
P AFB001 Afibrinogenemia 49 1.760
70
HPR003 Heparin-Induced Thrombocytopenia 49 1.760
71
c CNT016 Central Retinal Vein Occlusion 48 1.760
72
P BLD051 Blood Coagulation Disease 48 1.760
73
NDL013 Nodular Regenerative Hyperplasia 48 1.760
74
c RTN177 Retinitis Pigmentosa 73 47 1.760
75
c ACQ014 Acquired Hemophilia 47 1.760
76
LMR001 Lemierre's Syndrome 47 1.760
77
MLT113 Multicentric Castleman Disease 46 1.760
78
CTS005 Catastrophic Antiphospholipid Syndrome 44 1.760
79
P VND001 Vein Disease 43 1.760
80
THR035 Thrombasthenia 42 1.760
81
KRN001 Korean Hemorrhagic Fever 42 1.760
82
BRN026 Branch Retinal Artery Occlusion 41 1.760
83
MRN001 Marantic Endocarditis 40 1.760
84
LCH001 Leech Infestation 40 1.760
85
PRP028 Peripheral Vertigo 39 1.760
86
WTR001 Waterhouse-Friderichsen Syndrome 39 1.760
87
FRN014 Fournier Gangrene 38 1.760
88
c ACQ042 Acquired Hemophilia a 38 1.760
89
BLD009 Bladder Neck Obstruction 37 1.760
90
PRT012 Prothrombin Deficiency 37 1.760
91
URT016 Urethral Diverticulum 36 1.760
92
BLT003 Blue Toe Syndrome 36 1.760
93
FMR003 Femoral Neuropathy 36 1.760
94
SHW001 Shwartzman Phenomenon 35 1.760
95
SPL006 Splenic Infarction 35 1.760
96
P HPT020 Hepatic Vascular Disease 35 1.760
97
HMM001 Hemometra 35 1.760
98
c TRN014 Transient Arthritis 34 1.760
99
PLM180 Pulmonary Artery Disease 33 1.760
100
VRT001 Vertebral Artery Occlusion 33 1.760
101
CRB132 Cerebral Sinovenous Thrombosis 33 1.760
102
PRN016 Peroneal Neuropathy 33 1.760
103
DYS013 Dysbaric Osteonecrosis 32 1.760
104
HPT081 Hepatic Infarction 32 1.760
105
GNT005 Giant Hemangioma 31 1.760
106
c INH004 Inherited Blood Coagulation Disease 31 1.760
107
CNG016 Congenital Intrinsic Factor Deficiency 31 1.760
108
c ACT072 Acute Laryngitis 30 1.760
109
ANT022 Anterior Cranial Fossa Meningioma 28 1.760
110
QLT001 Qualitative Platelet Defect 28 1.760
111
TXC004 Toxic Diffuse Goiter 27 1.760
112
BNP002 Bone Epithelioid Hemangioma 26 1.760
113
INT050 Intestinal Impaction 26 1.760
114
END074 Endocardium Disease 25 1.760
115
CNJ001 Conjugate Gaze Palsy 25 1.760
116
BLV001 Bolivian Hemorrhagic Fever 25 1.760
117
SNL011 Snail Allergy 25 1.760
118
MXD019 Mixed Malaria 24 1.760
119
PDT002 Pediatric Meningioma 24 1.760
120
CRB017 Cerebral Falx Meningioma 23 1.760
121
WHT003 White Piedra 19 1.760
122
CHR051 Chorea Gravidarum 18 1.760
123
ART140 Arteries, Anomalies of 60 1.245
124
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.113
125
NNL006 Non-Alcoholic Steatohepatitis 53 0.101
126
FTT001 Fatty Liver Disease 63 0.087
127
P THL005 Thalassemia 62 0.087
128
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.087
129
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.087
130
P VSC018 Visceral Steatosis 34 0.087
131
c BTT014 Beta-Thalassemia 73 0.071
132
P HPT021 Hepatitis 69 0.071
133
P ASP006 Aspergillosis 67 0.071
134
DPR016 Depression 64 0.071
135
LSH001 Leishmaniasis 64 0.071
136
c HPT001 Hepatitis C 62 0.071
137
MNT002 Mental Depression 60 0.071
138
VSC003 Visceral Leishmaniasis 55 0.071
139
P AST007 Astrocytoma 52 0.071
140
HLX001 Helix Syndrome 46 0.071
141
P KLZ004 Kala-Azar 1 43 0.071
142
HMR044 Hamartoma, Precalcaneal Congenital Fibrolipomatous 12 0.071
143
P PRS040 Prostate Cancer 97 0.050
144
IMM167 Immune Deficiency Disease 79 0.050
145
c HPT073 Hepatitis C Virus 74 0.050
146
P CHR012 Chronic Granulomatous Disease 69 0.050
147
P MJR001 Major Depressive Disorder 69 0.050
148
P PRS038 Personality Disorder 66 0.050
149
LYM017 Lyme Disease 64 0.050
150
P GLM045 Glioma 64 0.050
151
c HPT016 Hepatitis B 63 0.050
152
c ALP101 Alpha-Thalassemia 63 0.050
153
P LMY004 Leiomyosarcoma 63 0.050
154
HYP066 Hyperglycemia 63 0.050
155
ADL002 Adult Syndrome 62 0.050
156
P BRN022 Bronchiectasis 60 0.050
157
P ALP008 Alopecia 58 0.050
158
APH002 Aphasia 56 0.050
159
DBT010 Diabetic Neuropathy 56 0.050
160
P PLY019 Polyneuropathy 55 0.050
161
NRT001 Neurotic Disorder 53 0.050
162
LMY002 Leiomyoma 52 0.050
163
P ALP061 Alopecia, Androgenetic, 1 51 0.050
164
P CRN276 Corneal Endothelial Dystrophy 50 0.050
165
SPL018 Splenomegaly 48 0.050
166
c INV001 Invasive Aspergillosis 48 0.050
167
DBT004 Diabetic Polyneuropathy 48 0.050
168
GLL048 Glial Tumor 48 0.050
169
FCH001 Fuchs' Endothelial Dystrophy 48 0.050
170
DYS009 Dysthymic Disorder 48 0.050
171
P CRN025 Corneal Dystrophy 45 0.050
172
SMT001 Somatization Disorder 45 0.050
173
DBT002 Diabetic Autonomic Neuropathy 45 0.050
174
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.050
175
AND014 Androgenic Alopecia 41 0.050
176
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 39 0.050
177
AGR018 Agraphia 38 0.050
178
GRN055 Granular Corneal Dystrophy 36 0.050
179
DYS003 Dysgraphia 34 0.050
180
PLY150 Polykaryocytosis Inducer 31 0.050
181
IRD003 Iridocorneal Endothelial Syndrome 28 0.050
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