Search results for F3

261 hits were found for F3

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 68 2.170
2
c SYS001 Systemic Lupus Erythematosus 86 2.113
3
LVR012 Liver Cirrhosis 62 1.911
4
P VSC007 Vascular Disease 63 1.854
5
MLR004 Malaria 81 1.830
6
STR067 Stroke, Ischemic 81 1.830
7
AST005 Asthma 76 1.830
8
P HRT032 Heart Disease 75 1.830
9
P KDN018 Kidney Disease 72 1.830
10
PRP027 Peripheral Vascular Disease 71 1.830
11
P MYC007 Myocardial Infarction 70 1.830
12
c HMP004 Hemophilia B 68 1.830
13
P THR014 Thrombocytopenia 67 1.830
14
FCT007 Factor Vii Deficiency 67 1.830
15
P PLM037 Pulmonary Hypertension 67 1.830
16
GLN010 Glanzmann Thrombasthenia 66 1.830
17
P VNW001 Von Willebrand's Disease 65 1.830
18
AFB002 Afibrinogenemia, Congenital 65 1.830
19
P HML002 Hemolytic Anemia 63 1.830
20
c PRC016 Pre-Eclampsia 63 1.830
21
ACT119 Acute Promyelocytic Leukemia 63 1.830
22
P THR005 Thrombotic Thrombocytopenic Purpura 61 1.830
23
FCT002 Factor Xi Deficiency 60 1.830
24
PLM033 Pulmonary Embolism 59 1.830
25
DSS009 Disseminated Intravascular Coagulation 57 1.830
26
c ACT075 Acute Myocardial Infarction 57 1.830
27
THR024 Thrombosis 57 1.830
28
P ANT006 Antiphospholipid Syndrome 55 1.830
29
FCT004 Factor Xii Deficiency 55 1.830
30
FCT003 Factor X Deficiency 54 1.830
31
P MNC007 Monocytic Leukemia 53 1.830
32
P HMR003 Hemorrhagic Disease 53 1.830
33
THR004 Thrombocytosis 51 1.830
34
P THR015 Thrombophilia 51 1.830
35
PRT014 Protein S Deficiency 44 1.830
36
CRT004 Carotid Artery Thrombosis 38 1.830
37
c HPT003 Hepatitis a 62 1.546
38
c THR092 Thrombophilia Due to Thrombin Defect 73 1.522
39
c HYP595 Hypertension, Essential 84 1.494
40
P RSP003 Respiratory Failure 74 1.494
41
P OST002 Osteoporosis 74 1.494
42
P HYP086 Hypothyroidism 69 1.494
43
P PNM007 Pneumonia 68 1.494
44
P ESS003 Essential Thrombocythemia 68 1.494
45
c HMP029 Hemophilia a 67 1.494
46
ANG054 Angina Pectoris 66 1.494
47
P ATR011 Atrial Fibrillation 66 1.494
48
ATH013 Atherosclerosis Susceptibility 65 1.494
49
P DBT009 Diabetes Mellitus 64 1.494
50
BDD001 Budd-Chiari Syndrome 63 1.494
51
TKY002 Takayasu Arteritis 62 1.494
52
LPP008 Lipoprotein Quantitative Trait Locus 62 1.494
53
TXC005 Toxic Shock Syndrome 62 1.494
54
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 1.494
55
P HMN010 Hemangioma 61 1.494
56
LNG099 Lung Disease 60 1.494
57
DNG002 Dengue Hemorrhagic Fever 60 1.494
58
PRT013 Portal Hypertension 59 1.494
59
SCR008 Scrub Typhus 58 1.494
60
BRS051 Breast Disease 58 1.494
61
FCT006 Factor V Deficiency 57 1.494
62
P CRD246 Cardiovascular System Disease 57 1.494
63
PLC005 Placental Insufficiency 57 1.494
64
HPT046 Hepatic Veno-Occlusive Disease 56 1.494
65
PRP030 Purpura 54 1.494
66
PYD001 Pyoderma Gangrenosum 54 1.494
67
P INF037 Inflammatory Bowel Disease 54 1.494
68
P ART021 Arteriosclerosis 54 1.494
69
HLL004 Hellp Syndrome 54 1.494
70
CRM001 Crimean-Congo Hemorrhagic Fever 53 1.494
71
c CNT016 Central Retinal Vein Occlusion 53 1.494
72
P HML001 Hemolytic-Uremic Syndrome 53 1.494
73
INT075 Intracranial Hypertension 53 1.494
74
P RTN022 Retinal Vein Occlusion 53 1.494
75
PRP080 Peripheral Artery Disease 53 1.494
76
FCT005 Factor Xiii Deficiency 52 1.494
77
P CHL066 Cholangitis 51 1.494
78
HNT002 Hantavirus Pulmonary Syndrome 50 1.494
79
MYC087 Mycoplasma Pneumoniae Pneumonia 50 1.494
80
PYD002 Pyoderma 50 1.494
81
PLC008 Placenta Disease 50 1.494
82
NPH010 Nephrosclerosis 50 1.494
83
BLD053 Blood Platelet Disease 49 1.494
84
INT078 Intracranial Thrombosis 49 1.494
85
c VNW005 Von Willebrand Disease, Type 1 48 1.494
86
CRN017 Coronary Thrombosis 47 1.494
87
SPC010 Speech and Communication Disorders 47 1.494
88
P PRP034 Purpura Fulminans 43 1.494
89
CRT012 Cortical Blindness 37 1.494
90
PRP028 Peripheral Vertigo 37 1.494
91
SGT001 Sagittal Sinus Thrombosis 32 1.494
92
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 1.057
93
PTN001 Patent Foramen Ovale 60 1.057
94
P ATR010 Atrial Heart Septal Defect 60 1.057
95
P BRN019 Bernard-Soulier Syndrome 60 1.057
96
ANT009 Antithrombin Iii Deficiency 59 1.057
97
P MTR012 Mitral Valve Disease 58 1.057
98
P MYM013 Moyamoya Disease 1 57 1.057
99
P EXN002 Exanthem 57 1.057
100
BLR008 Bilirubin Metabolic Disorder 57 1.057
101
INT303 Intracranial Hypertension, Idiopathic 57 1.057
102
ACT058 Active Peptic Ulcer Disease 55 1.057
103
INT007 Intermediate Coronary Syndrome 55 1.057
104
ANL018 Analbuminemia 54 1.057
105
CRT016 Carotid Artery Disease 52 1.057
106
ART140 Arteries, Anomalies of 52 1.057
107
FCT001 Factor Viii Deficiency 51 1.057
108
THR016 Thrombophlebitis 51 1.057
109
ESP002 Esophageal Varix 51 1.057
110
P PRC012 Pericardial Effusion 51 1.057
111
P PST095 Post-Thrombotic Syndrome 51 1.057
112
P MTR003 Mitral Valve Stenosis 50 1.057
113
c ACQ017 Acquired Von Willebrand Syndrome 49 1.057
114
PPL021 Papilledema 49 1.057
115
P CMP008 Compartment Syndrome 49 1.057
116
EBL001 Ebola Hemorrhagic Fever 49 1.057
117
ASP007 Aspiration Pneumonia 48 1.057
118
VTM033 Vitamin K Deficiency Bleeding 48 1.057
119
HMP001 Hemopericardium 48 1.057
120
INT010 Intracranial Embolism 48 1.057
121
HPR003 Heparin-Induced Thrombocytopenia 48 1.057
122
CRD001 Cardiac Tamponade 47 1.057
123
MLT113 Multicentric Castleman Disease 47 1.057
124
NDL013 Nodular Regenerative Hyperplasia 47 1.057
125
SPL012 Splenic Disease 47 1.057
126
P BLD051 Blood Coagulation Disease 46 1.057
127
MDS022 Mediastinitis 46 1.057
128
ANR004 Anuria 46 1.057
129
c TRC022 Tricuspid Valve Insufficiency 45 1.057
130
HPT004 Hepatic Coma 45 1.057
131
HMR002 Hemarthrosis 45 1.057
132
c ACQ014 Acquired Hemophilia 45 1.057
133
ASP008 Aspiration Pneumonitis 45 1.057
134
P TRC087 Tricuspid Valve Disease 44 1.057
135
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 1.057
136
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 44 1.057
137
ANG011 Angiodysplasia 43 1.057
138
P VND001 Vein Disease 42 1.057
139
LMR001 Lemierre's Syndrome 42 1.057
140
CTS005 Catastrophic Antiphospholipid Syndrome 42 1.057
141
HGH020 High Molecular Weight Kininogen Deficiency 41 1.057
142
THR035 Thrombasthenia 40 1.057
143
PRT012 Prothrombin Deficiency 40 1.057
144
P INT260 Intracranial Berry Aneurysm 39 1.057
145
RCK002 Rocky Mountain Spotted Fever 39 1.057
146
c PRM225 Primary Thrombocytopenia 39 1.057
147
SPL006 Splenic Infarction 38 1.057
148
BLD054 Blood Protein Disease 38 1.057
149
MRN001 Marantic Endocarditis 38 1.057
150
SHW001 Shwartzman Phenomenon 37 1.057
151
FRN014 Fournier Gangrene 37 1.057
152
c ACQ042 Acquired Hemophilia a 37 1.057
153
WTR001 Waterhouse-Friderichsen Syndrome 36 1.057
154
ACT056 Acute Cor Pulmonale 36 1.057
155
EPD005 Epidural Abscess 35 1.057
156
SPL009 Splenic Sequestration 35 1.057
157
LCH001 Leech Infestation 35 1.057
158
INT003 Intracranial Hypotension 35 1.057
159
P HPT020 Hepatic Vascular Disease 34 1.057
160
CNG016 Congenital Intrinsic Factor Deficiency 34 1.057
161
HMP003 Hemopneumothorax 33 1.057
162
PLM180 Pulmonary Artery Disease 33 1.057
163
CRB132 Cerebral Sinovenous Thrombosis 33 1.057
164
HPT081 Hepatic Infarction 33 1.057
165
CVR002 Cavernous Sinus Thrombosis 33 1.057
166
HRT008 Heart Conduction Disease 32 1.057
167
CRT009 Critical Illness Polyneuropathy 32 1.057
168
LJH001 Lujo Hemorrhagic Fever 31 1.057
169
c PST018 Posterior Cerebral Artery Infarction 31 1.057
170
CCL002 Cecal Disease 31 1.057
171
FMR003 Femoral Neuropathy 31 1.057
172
EMP002 Emphysematous Cholecystitis 30 1.057
173
c INH004 Inherited Blood Coagulation Disease 30 1.057
174
BLT003 Blue Toe Syndrome 29 1.057
175
INT076 Intracranial Sinus Thrombosis 29 1.057
176
P PRC050 Pericardium Disease 29 1.057
177
THR007 Thrombophlebitis Migrans 29 1.057
178
LTR002 Lateral Sinus Thrombosis 29 1.057
179
QLT001 Qualitative Platelet Defect 29 1.057
180
GNT005 Giant Hemangioma 28 1.057
181
SYN004 Synovial Angioma 27 1.057
182
XLN228 X-Linked Recessive Disease 26 1.057
183
VLV018 Vulvar Angiokeratoma 26 1.057
184
PPL016 Papillary Adenofibroma 26 1.057
185
OCC005 Occlusion Precerebral Artery 26 1.057
186
CRB017 Cerebral Falx Meningioma 26 1.057
187
GST005 Gastric Hemangioma 26 1.057
188
ATM012 Autoimmune Disease of Blood 25 1.057
189
DCN001 Dic in Newborn 24 1.057
190
PLY003 Polycystic Echinococcosis 24 1.057
191
ACT065 Acute Hemorrhagic Encephalitis 24 1.057
192
RNL009 Renal Pelvis Squamous Cell Carcinoma 24 1.057
193
c ATM013 Autoimmune Disease of Cardiovascular System 24 1.057
194
c ANK021 Ankylosing Spondylitis 1 23 1.057
195
CFT003 Ceftriaxone Allergy 23 1.057
196
ALK001 Alkhurma Hemorrhagic Fever 22 1.057
197
END074 Endocardium Disease 22 1.057
198
DBT003 Diabetic Peripheral Angiopathy 22 1.057
199
ACH007 Achenbach Syndrome 22 1.057
200
P ACT080 Acute Pulmonary Heart Disease 22 1.057
201
MDL001 Medulloadrenal Hyperfunction 22 1.057
202
AST001 Astrakhan Spotted Fever 17 1.057
203
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.099
204
NNL006 Non-Alcoholic Steatohepatitis 54 0.088
205
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.076
206
FTT001 Fatty Liver Disease 61 0.076
207
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.076
208
P THL005 Thalassemia 60 0.076
209
P VSC018 Visceral Steatosis 33 0.076
210
c BTT014 Beta-Thalassemia 74 0.062
211
P ASP006 Aspergillosis 69 0.062
212
P HPT021 Hepatitis 67 0.062
213
LSH001 Leishmaniasis 63 0.062
214
DPR016 Depression 63 0.062
215
c HPT001 Hepatitis C 62 0.062
216
MNT002 Mental Depression 58 0.062
217
VSC003 Visceral Leishmaniasis 55 0.062
218
P AST007 Astrocytoma 51 0.062
219
HLX001 Helix Syndrome 47 0.062
220
P KLZ004 Kala-Azar 1 41 0.062
221
HMR044 Hamartoma, Precalcaneal Congenital Fibrolipomatous 13 0.062
222
P PRS040 Prostate Cancer 97 0.044
223
IMM167 Immune Deficiency Disease 78 0.044
224
CRV035 Cervical Cancer 76 0.044
225
c HPT073 Hepatitis C Virus 72 0.044
226
ADL002 Adult Syndrome 70 0.044
227
P MJR001 Major Depressive Disorder 68 0.044
228
P CHR012 Chronic Granulomatous Disease 67 0.044
229
P PRS038 Personality Disorder 65 0.044
230
LYM017 Lyme Disease 64 0.044
231
P GLM045 Glioma 63 0.044
232
P LMY004 Leiomyosarcoma 63 0.044
233
c ALP101 Alpha-Thalassemia 62 0.044
234
HYP066 Hyperglycemia 61 0.044
235
c HPT016 Hepatitis B 59 0.044
236
P BRN022 Bronchiectasis 59 0.044
237
APH002 Aphasia 57 0.044
238
P FTL001 Fetal Alcohol Syndrome 57 0.044
239
P PLY019 Polyneuropathy 56 0.044
240
P ALP008 Alopecia 54 0.044
241
DBT010 Diabetic Neuropathy 54 0.044
242
NRT001 Neurotic Disorder 53 0.044
243
P CRN276 Corneal Endothelial Dystrophy 52 0.044
244
LMY002 Leiomyoma 52 0.044
245
DBT004 Diabetic Polyneuropathy 49 0.044
246
P CRN025 Corneal Dystrophy 49 0.044
247
DYS009 Dysthymic Disorder 49 0.044
248
P ALP061 Alopecia, Androgenetic, 1 49 0.044
249
c INV001 Invasive Aspergillosis 49 0.044
250
SPL018 Splenomegaly 48 0.044
251
SMT001 Somatization Disorder 46 0.044
252
AND014 Androgenic Alopecia 46 0.044
253
GLL048 Glial Tumor 45 0.044
254
FCH001 Fuchs' Endothelial Dystrophy 44 0.044
255
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.044
256
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.044
257
DBT002 Diabetic Autonomic Neuropathy 41 0.044
258
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 37 0.044
259
DYS003 Dysgraphia 36 0.044
260
AGR018 Agraphia 34 0.044
261
PLY150 Polykaryocytosis Inducer 31 0.044
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