Search results for F3

246 hits were found for F3

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 68 2.239
2
c SYS001 Systemic Lupus Erythematosus 87 2.181
3
LVR012 Liver Cirrhosis 64 1.972
4
P VSC007 Vascular Disease 64 1.913
5
MLR004 Malaria 81 1.889
6
STR067 Stroke, Ischemic 80 1.889
7
AST005 Asthma 77 1.889
8
P HRT032 Heart Disease 76 1.889
9
P MYC007 Myocardial Infarction 71 1.889
10
P KDN018 Kidney Disease 71 1.889
11
P PLM037 Pulmonary Hypertension 69 1.889
12
P THR014 Thrombocytopenia 68 1.889
13
c HMP004 Hemophilia B 68 1.889
14
FCT007 Factor Vii Deficiency 67 1.889
15
GLN010 Glanzmann Thrombasthenia 67 1.889
16
AFB002 Afibrinogenemia, Congenital 65 1.889
17
P VNW001 Von Willebrand's Disease 65 1.889
18
c PRC016 Pre-Eclampsia 64 1.889
19
ACT119 Acute Promyelocytic Leukemia 63 1.889
20
P HML002 Hemolytic Anemia 63 1.889
21
P THR005 Thrombotic Thrombocytopenic Purpura 62 1.889
22
FCT002 Factor Xi Deficiency 60 1.889
23
PLM033 Pulmonary Embolism 59 1.889
24
DSS009 Disseminated Intravascular Coagulation 58 1.889
25
THR024 Thrombosis 57 1.889
26
c ACT075 Acute Myocardial Infarction 57 1.889
27
FCT003 Factor X Deficiency 56 1.889
28
P ANT006 Antiphospholipid Syndrome 55 1.889
29
FCT004 Factor Xii Deficiency 55 1.889
30
P MNC007 Monocytic Leukemia 54 1.889
31
P HMR003 Hemorrhagic Disease 53 1.889
32
THR004 Thrombocytosis 51 1.889
33
P THR015 Thrombophilia 51 1.889
34
PRT014 Protein S Deficiency 51 1.889
35
CRT004 Carotid Artery Thrombosis 38 1.889
36
c HPT003 Hepatitis a 63 1.595
37
c THR092 Thrombophilia Due to Thrombin Defect 73 1.571
38
c HYP595 Hypertension, Essential 85 1.542
39
P RSP003 Respiratory Failure 75 1.542
40
P OST002 Osteoporosis 74 1.542
41
PRP027 Peripheral Vascular Disease 72 1.542
42
P ESS003 Essential Thrombocythemia 70 1.542
43
P HYP086 Hypothyroidism 69 1.542
44
P PNM007 Pneumonia 68 1.542
45
P ATR011 Atrial Fibrillation 66 1.542
46
ANG054 Angina Pectoris 66 1.542
47
ATH013 Atherosclerosis Susceptibility 66 1.542
48
c HMP029 Hemophilia a 65 1.542
49
P DBT009 Diabetes Mellitus 65 1.542
50
P CRN018 Coronary Artery Anomaly 64 1.542
51
BDD001 Budd-Chiari Syndrome 62 1.542
52
TXC005 Toxic Shock Syndrome 62 1.542
53
TKY002 Takayasu Arteritis 62 1.542
54
P HMN010 Hemangioma 62 1.542
55
LNG099 Lung Disease 61 1.542
56
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 1.542
57
PRT013 Portal Hypertension 61 1.542
58
DNG002 Dengue Hemorrhagic Fever 60 1.542
59
SCR008 Scrub Typhus 59 1.542
60
BRS051 Breast Disease 58 1.542
61
PLC005 Placental Insufficiency 57 1.542
62
HPT046 Hepatic Veno-Occlusive Disease 57 1.542
63
P CRD246 Cardiovascular System Disease 56 1.542
64
FCT006 Factor V Deficiency 56 1.542
65
P INF037 Inflammatory Bowel Disease 56 1.542
66
PRP030 Purpura 56 1.542
67
PYD001 Pyoderma Gangrenosum 55 1.542
68
P ART021 Arteriosclerosis 55 1.542
69
HLL004 Hellp Syndrome 54 1.542
70
INT075 Intracranial Hypertension 54 1.542
71
FCT005 Factor Xiii Deficiency 53 1.542
72
PRP080 Peripheral Artery Disease 53 1.542
73
P HML001 Hemolytic-Uremic Syndrome 53 1.542
74
P RTN022 Retinal Vein Occlusion 52 1.542
75
CRM001 Crimean-Congo Hemorrhagic Fever 52 1.542
76
PYD002 Pyoderma 52 1.542
77
BLD053 Blood Platelet Disease 51 1.542
78
MYC087 Mycoplasma Pneumoniae Pneumonia 50 1.542
79
NPH010 Nephrosclerosis 50 1.542
80
c CNT016 Central Retinal Vein Occlusion 50 1.542
81
PLC008 Placenta Disease 50 1.542
82
INT078 Intracranial Thrombosis 49 1.542
83
c VNW005 Von Willebrand Disease, Type 1 49 1.542
84
SPC010 Speech and Communication Disorders 48 1.542
85
HNT002 Hantavirus Pulmonary Syndrome 48 1.542
86
CRN017 Coronary Thrombosis 47 1.542
87
P PRP034 Purpura Fulminans 42 1.542
88
CRT012 Cortical Blindness 39 1.542
89
PRP028 Peripheral Vertigo 39 1.542
90
SGT001 Sagittal Sinus Thrombosis 33 1.542
91
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 1.090
92
P ATR010 Atrial Heart Septal Defect 61 1.090
93
BLR008 Bilirubin Metabolic Disorder 58 1.090
94
P EXN002 Exanthem 58 1.090
95
INT303 Intracranial Hypertension, Idiopathic 57 1.090
96
PTN001 Patent Foramen Ovale 56 1.090
97
GRN034 Grange Syndrome 56 1.090
98
ACT058 Active Peptic Ulcer Disease 55 1.090
99
INT007 Intermediate Coronary Syndrome 55 1.090
100
FCT001 Factor Viii Deficiency 55 1.090
101
P MYM013 Moyamoya Disease 1 55 1.090
102
ANL018 Analbuminemia 54 1.090
103
HRT012 Heart Valve Disease 53 1.090
104
ART140 Arteries, Anomalies of 53 1.090
105
CRT016 Carotid Artery Disease 52 1.090
106
THR016 Thrombophlebitis 52 1.090
107
ESP002 Esophageal Varix 51 1.090
108
P PRC012 Pericardial Effusion 51 1.090
109
P PST095 Post-Thrombotic Syndrome 51 1.090
110
P MTR003 Mitral Valve Stenosis 51 1.090
111
c ACQ017 Acquired Von Willebrand Syndrome 50 1.090
112
NCR007 Necrotizing Fasciitis 49 1.090
113
PPL021 Papilledema 49 1.090
114
P CMP008 Compartment Syndrome 49 1.090
115
VTM033 Vitamin K Deficiency Bleeding 49 1.090
116
ASP007 Aspiration Pneumonia 48 1.090
117
SPL012 Splenic Disease 48 1.090
118
HPR003 Heparin-Induced Thrombocytopenia 48 1.090
119
NDL013 Nodular Regenerative Hyperplasia 47 1.090
120
CRD001 Cardiac Tamponade 47 1.090
121
P BLD051 Blood Coagulation Disease 47 1.090
122
HMP001 Hemopericardium 47 1.090
123
ANR004 Anuria 46 1.090
124
EBL001 Ebola Hemorrhagic Fever 46 1.090
125
P TRC087 Tricuspid Valve Disease 46 1.090
126
INT010 Intracranial Embolism 46 1.090
127
MLT113 Multicentric Castleman Disease 46 1.090
128
c TRC022 Tricuspid Valve Insufficiency 46 1.090
129
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 45 1.090
130
c ACQ014 Acquired Hemophilia 45 1.090
131
HMR002 Hemarthrosis 45 1.090
132
BRN026 Branch Retinal Artery Occlusion 43 1.090
133
ANG011 Angiodysplasia 43 1.090
134
P VND001 Vein Disease 43 1.090
135
ASP008 Aspiration Pneumonitis 43 1.090
136
CTS005 Catastrophic Antiphospholipid Syndrome 42 1.090
137
THR035 Thrombasthenia 41 1.090
138
PRT012 Prothrombin Deficiency 41 1.090
139
RCK002 Rocky Mountain Spotted Fever 40 1.090
140
LMR001 Lemierre's Syndrome 40 1.090
141
c PRM225 Primary Thrombocytopenia 40 1.090
142
P INT260 Intracranial Berry Aneurysm 39 1.090
143
BLD054 Blood Protein Disease 38 1.090
144
MRN001 Marantic Endocarditis 38 1.090
145
FRN014 Fournier Gangrene 37 1.090
146
SPL006 Splenic Infarction 37 1.090
147
c ACQ042 Acquired Hemophilia a 37 1.090
148
SHW001 Shwartzman Phenomenon 37 1.090
149
SPL009 Splenic Sequestration 37 1.090
150
LCH001 Leech Infestation 36 1.090
151
EPD005 Epidural Abscess 36 1.090
152
ACT056 Acute Cor Pulmonale 36 1.090
153
CNG016 Congenital Intrinsic Factor Deficiency 35 1.090
154
PLM180 Pulmonary Artery Disease 35 1.090
155
P HPT020 Hepatic Vascular Disease 33 1.090
156
INT003 Intracranial Hypotension 33 1.090
157
CRB132 Cerebral Sinovenous Thrombosis 33 1.090
158
HPT081 Hepatic Infarction 33 1.090
159
VLK001 Volkmann Contracture 32 1.090
160
THR007 Thrombophlebitis Migrans 32 1.090
161
HRT008 Heart Conduction Disease 32 1.090
162
c INH004 Inherited Blood Coagulation Disease 31 1.090
163
BLT003 Blue Toe Syndrome 31 1.090
164
FMR003 Femoral Neuropathy 31 1.090
165
LJH001 Lujo Hemorrhagic Fever 31 1.090
166
QLT001 Qualitative Platelet Defect 31 1.090
167
P PRC050 Pericardium Disease 30 1.090
168
INT076 Intracranial Sinus Thrombosis 29 1.090
169
EMP002 Emphysematous Cholecystitis 29 1.090
170
FCT008 Factitious Disorder 28 1.090
171
c BNG012 Benign Mesenchymoma 28 1.090
172
SYN004 Synovial Angioma 27 1.090
173
GNT005 Giant Hemangioma 27 1.090
174
PPL016 Papillary Adenofibroma 27 1.090
175
ATM012 Autoimmune Disease of Blood 26 1.090
176
XLN228 X-Linked Recessive Disease 26 1.090
177
OCC005 Occlusion Precerebral Artery 26 1.090
178
END074 Endocardium Disease 26 1.090
179
c ACQ001 Acquired Color Blindness 25 1.090
180
DCN001 Dic in Newborn 24 1.090
181
PLY003 Polycystic Echinococcosis 24 1.090
182
RNL009 Renal Pelvis Squamous Cell Carcinoma 23 1.090
183
DBT003 Diabetic Peripheral Angiopathy 22 1.090
184
GST005 Gastric Hemangioma 22 1.090
185
P ACT080 Acute Pulmonary Heart Disease 22 1.090
186
c ACQ004 Acquired Hemangioma 22 1.090
187
VLV018 Vulvar Angiokeratoma 18 1.090
188
AST001 Astrakhan Spotted Fever 17 1.090
189
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.111
190
NNL006 Non-Alcoholic Steatohepatitis 51 0.091
191
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.079
192
FTT001 Fatty Liver Disease 62 0.079
193
P THL005 Thalassemia 60 0.079
194
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.079
195
P VSC018 Visceral Steatosis 33 0.079
196
c BTT014 Beta-Thalassemia 73 0.064
197
P HPT021 Hepatitis 68 0.064
198
P ASP006 Aspergillosis 67 0.064
199
DPR016 Depression 64 0.064
200
LSH001 Leishmaniasis 64 0.064
201
c HPT001 Hepatitis C 63 0.064
202
MNT002 Mental Depression 57 0.064
203
VSC003 Visceral Leishmaniasis 55 0.064
204
P AST007 Astrocytoma 50 0.064
205
HLX001 Helix Syndrome 48 0.064
206
P KLZ004 Kala-Azar 1 42 0.064
207
HMR044 Hamartoma, Precalcaneal Congenital Fibrolipomatous 13 0.064
208
P PRS040 Prostate Cancer 98 0.045
209
IMM167 Immune Deficiency Disease 78 0.045
210
c HPT073 Hepatitis C Virus 71 0.045
211
ADL002 Adult Syndrome 70 0.045
212
P MJR001 Major Depressive Disorder 68 0.045
213
P CHR012 Chronic Granulomatous Disease 68 0.045
214
P PRS038 Personality Disorder 65 0.045
215
LYM017 Lyme Disease 64 0.045
216
P GLM045 Glioma 63 0.045
217
P LMY004 Leiomyosarcoma 63 0.045
218
c ALP101 Alpha-Thalassemia 62 0.045
219
HYP066 Hyperglycemia 61 0.045
220
P BRN022 Bronchiectasis 60 0.045
221
c HPT016 Hepatitis B 60 0.045
222
APH002 Aphasia 57 0.045
223
P ALP008 Alopecia 56 0.045
224
P PLY019 Polyneuropathy 56 0.045
225
P FTL001 Fetal Alcohol Syndrome 55 0.045
226
DBT010 Diabetic Neuropathy 55 0.045
227
NRT001 Neurotic Disorder 53 0.045
228
LMY002 Leiomyoma 51 0.045
229
DBT004 Diabetic Polyneuropathy 51 0.045
230
P CRN276 Corneal Endothelial Dystrophy 50 0.045
231
P ALP061 Alopecia, Androgenetic, 1 50 0.045
232
c INV001 Invasive Aspergillosis 49 0.045
233
SPL018 Splenomegaly 48 0.045
234
DYS009 Dysthymic Disorder 48 0.045
235
SMT001 Somatization Disorder 48 0.045
236
FCH001 Fuchs' Endothelial Dystrophy 47 0.045
237
P CRN025 Corneal Dystrophy 46 0.045
238
GLL048 Glial Tumor 46 0.045
239
AND014 Androgenic Alopecia 45 0.045
240
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.045
241
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.045
242
DBT002 Diabetic Autonomic Neuropathy 41 0.045
243
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 38 0.045
244
DYS003 Dysgraphia 35 0.045
245
AGR018 Agraphia 32 0.045
246
PLY150 Polykaryocytosis Inducer 31 0.045
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