Search results for f2

240 hits were found for f2

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 54 3.711
2
P LVR013 Liver Disease 75 2.744
3
STR067 Stroke, Ischemic 75 2.604
4
c THR092 Thrombophilia Due to Thrombin Defect 54 2.589
5
P HPT021 Hepatitis 69 2.540
6
LVR012 Liver Cirrhosis 67 2.540
7
c HPT016 Hepatitis B 64 2.540
8
ALC006 Alcoholic Hepatitis 59 2.540
9
PRG096 Pregnancy Loss, Recurrent 2 21 2.387
10
P THR015 Thrombophilia 59 2.356
11
P HPT023 Hepatocellular Carcinoma 92 2.319
12
P ATR011 Atrial Fibrillation 66 2.319
13
P THR014 Thrombocytopenia 64 2.319
14
c HMP029 Hemophilia a 63 2.319
15
c HMP004 Hemophilia B 62 2.319
16
FCT003 Factor X Deficiency 61 2.319
17
VNW001 Von Willebrand's Disease 61 2.319
18
FCT007 Factor Vii Deficiency 61 2.319
19
P PRT013 Portal Hypertension 60 2.319
20
PLM033 Pulmonary Embolism 60 2.319
21
c VRL010 Viral Hepatitis 60 2.319
22
c ATM011 Autoimmune Hepatitis 60 2.319
23
THR024 Thrombosis 57 2.319
24
P HMR003 Hemorrhagic Disease 57 2.319
25
P ANT006 Antiphospholipid Syndrome 56 2.319
26
HPT019 Hepatic Encephalopathy 56 2.319
27
THR004 Thrombocytosis 55 2.319
28
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 2.319
29
PRT014 Protein S Deficiency 53 2.319
30
PRT011 Protein C Deficiency 52 2.319
31
P PRM006 Primary Biliary Cirrhosis 51 2.319
32
DSS009 Disseminated Intravascular Coagulation 51 2.319
33
c ACT134 Acute Liver Failure 50 2.319
34
ALC009 Alcoholic Liver Cirrhosis 49 2.319
35
PRT018 Portal Vein Thrombosis 49 2.319
36
HYP063 Hypersplenism 48 2.319
37
HPT014 Hepatorenal Syndrome 46 2.319
38
c PRT045 Prothrombin-Related Thrombophilia 24 2.114
39
SCK003 Sickle Cell Anemia 71 2.074
40
PRP027 Peripheral Vascular Disease 68 2.074
41
CRB037 Cerebral Palsy 66 2.074
42
DNG002 Dengue Hemorrhagic Fever 63 2.074
43
GLN010 Glanzmann Thrombasthenia 63 2.074
44
PRT036 Peritonitis 63 2.074
45
LPT001 Leptospirosis 62 2.074
46
P ADL010 Adult Respiratory Distress Syndrome 61 2.074
47
c HPT003 Hepatitis a 59 2.074
48
CHL068 Cholestasis 59 2.074
49
PRP030 Purpura 58 2.074
50
SCH014 Schistosomiasis 58 2.074
51
FCT006 Factor V Deficiency 57 2.074
52
CHL067 Cholecystitis 57 2.074
53
INT002 Intermittent Claudication 56 2.074
54
P BDD001 Budd-Chiari Syndrome 56 2.074
55
PTN001 Patent Foramen Ovale 55 2.074
56
PLM010 Pulmonary Edema 54 2.074
57
c HPT007 Hepatitis E 54 2.074
58
P END033 Endocarditis 54 2.074
59
c AFB002 Afibrinogenemia, Congenital 54 2.074
60
P ECL001 Eclampsia 54 2.074
61
P VNS003 Venous Insufficiency 54 2.074
62
SCT005 Scott Syndrome 53 2.074
63
BRG013 Buerger Disease 53 2.074
64
SPT005 Spotted Fever 53 2.074
65
THR016 Thrombophlebitis 53 2.074
66
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 2.074
67
c HPT015 Hepatitis D 52 2.074
68
INF034 Infective Endocarditis 51 2.074
69
INT075 Intracranial Hypertension 50 2.074
70
BRN082 Bernard-Soulier Syndrome, Type C 50 2.074
71
PLC005 Placental Insufficiency 50 2.074
72
HLL004 Hellp Syndrome 50 2.074
73
P SCK002 Sick Sinus Syndrome 50 2.074
74
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 2.074
75
OBS001 Obstructive Jaundice 48 2.074
76
P CMP008 Compartment Syndrome 48 2.074
77
VND001 Vein Disease 47 2.074
78
PPL021 Papilledema 47 2.074
79
PLC007 Placental Abruption 47 2.074
80
PST095 Post-Thrombotic Syndrome 47 2.074
81
CVR006 Cavernous Hemangioma 46 2.074
82
OST003 Osteonecrosis 45 2.074
83
SND002 Sneddon Syndrome 44 2.074
84
c HMG003 Hemoglobin E Disease 44 2.074
85
P RTN014 Retinal Artery Occlusion 44 2.074
86
HPT008 Hepatic Tuberculosis 42 2.074
87
BLR008 Bilirubin Metabolic Disorder 42 2.074
88
P CHL066 Cholangitis 42 2.074
89
ESP002 Esophageal Varix 41 2.074
90
P PRP034 Purpura Fulminans 41 2.074
91
ISC015 Ischemic Colitis 39 2.074
92
HPT004 Hepatic Coma 39 2.074
93
P RTN022 Retinal Vein Occlusion 38 2.074
94
c CNT016 Central Retinal Vein Occlusion 36 2.074
95
SGT001 Sagittal Sinus Thrombosis 35 2.074
96
CHL039 Choledocholithiasis 34 2.074
97
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 2.074
98
CRB132 Cerebral Sinovenous Thrombosis 31 1.820
99
P OBS005 Obesity 92 1.796
100
P PLM037 Pulmonary Hypertension 79 1.796
101
P MYC007 Myocardial Infarction 79 1.796
102
P RSP003 Respiratory Failure 71 1.796
103
CRB039 Cerebrovascular Disease 63 1.796
104
P HMP007 Hemophilia 57 1.796
105
P HMR012 Hemorrhagic Fever 56 1.796
106
ART111 Artery Disease 55 1.796
107
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 1.796
108
HNT002 Hantavirus Pulmonary Syndrome 51 1.796
109
IMM136 Immune System Disease 51 1.796
110
STR081 Stormorken Syndrome 49 1.796
111
VNW005 Von Willebrand Disease, Type 1 49 1.796
112
P AFB001 Afibrinogenemia 48 1.796
113
VLV011 Vulvovaginal Candidiasis 48 1.796
114
P PRN026 Porencephaly 48 1.796
115
SPL012 Splenic Disease 46 1.796
116
P DYS026 Dysfibrinogenemia 45 1.796
117
P ANL018 Analbuminemia 44 1.796
118
CRD001 Cardiac Tamponade 44 1.796
119
c SVR056 Severe Hemophilia a 43 1.796
120
ACT058 Active Peptic Ulcer Disease 43 1.796
121
HRT008 Heart Conduction Disease 42 1.796
122
HPT020 Hepatic Vascular Disease 42 1.796
123
P BLD051 Blood Coagulation Disease 42 1.796
124
c CHR064 Chronic Monocytic Leukemia 42 1.796
125
MRB001 Marburg Hemorrhagic Fever 41 1.796
126
KWS001 Kwashiorkor 40 1.796
127
ENT001 Enterocele 40 1.796
128
SQM002 Squamous Cell Papilloma 40 1.796
129
LCH001 Leech Infestation 40 1.796
130
KRN001 Korean Hemorrhagic Fever 39 1.796
131
CHR466 Chronic Thromboembolic Pulmonary Hypertension 39 1.796
132
THR035 Thrombasthenia 39 1.796
133
BRN026 Branch Retinal Artery Occlusion 38 1.796
134
HYP016 Hypochondriasis 38 1.796
135
FMR003 Femoral Neuropathy 38 1.796
136
PRP028 Peripheral Vertigo 38 1.796
137
BLD054 Blood Protein Disease 37 1.796
138
BSL004 Basilar Artery Occlusion 36 1.796
139
c INH004 Inherited Blood Coagulation Disease 36 1.796
140
ISC005 Ischemic Bone Disease 36 1.796
141
BLT003 Blue Toe Syndrome 35 1.796
142
GNT005 Giant Hemangioma 35 1.796
143
FRN014 Fournier Gangrene 35 1.796
144
HMC014 Homocysteinemia 35 1.796
145
SPL006 Splenic Infarction 35 1.796
146
FRY001 Frey Syndrome 35 1.796
147
END013 Endometrial Small Cell Carcinoma 34 1.796
148
MSN003 Mesenteric Vascular Occlusion 34 1.796
149
SPN185 Spinal Cord Infarction 34 1.796
150
ANT013 Anterior Spinal Artery Syndrome 33 1.796
151
ABD004 Abdominal Tuberculosis 32 1.796
152
RTN021 Retinal Vascular Occlusion 32 1.796
153
LVD002 Livedoid Vasculopathy 32 1.796
154
MRN001 Marantic Endocarditis 32 1.796
155
ORB007 Orbital Cyst 32 1.796
156
SBN001 Subendocardial Myocardial Infarction 32 1.796
157
INT010 Intracranial Embolism 32 1.796
158
QLT001 Qualitative Platelet Defect 32 1.796
159
PLS002 Peliosis Hepatis 31 1.796
160
INT050 Intestinal Impaction 31 1.796
161
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 1.796
162
SDD008 Sudden Sensorineural Hearing Loss 31 1.796
163
URT011 Urethral Calculus 31 1.796
164
VSC008 Vascular Hemostatic Disease 30 1.796
165
ASC003 Ascending Cholangitis 30 1.796
166
ISC001 Ischemic Neuropathy 30 1.796
167
EXH001 Exhibitionism 29 1.796
168
EPS001 Epstein-Barr Virus Hepatitis 29 1.796
169
MXL016 Maxillonasal Dysplasia, Binder Type 28 1.796
170
SPR011 Suprasellar Meningioma 28 1.796
171
ANT022 Anterior Cranial Fossa Meningioma 28 1.796
172
PRM008 Parametritis 27 1.796
173
PRC051 Paracetamol Poisoning 27 1.796
174
ECC005 Eccrine Adenocarcinoma 27 1.796
175
c MLG042 Malignant Otitis Externa 26 1.796
176
TYL001 Taylor's Syndrome 26 1.796
177
CNR001 Coenurosis 25 1.796
178
c ANT010 Anterior Compartment Syndrome 25 1.796
179
PHN001 Phencyclidine Abuse 22 1.796
180
NNH002 Non-a-E Hepatitis 21 1.796
181
CRB017 Cerebral Falx Meningioma 21 1.796
182
PRL015 Prolapse of Female Genital Organ 21 1.796
183
HPT066 Hepatoportal Sclerosis 20 1.796
184
HLR004 Hilar Cholangiocellular Carcinoma 14 1.796
185
URT015 Urethral False Passage 11 1.796
186
P ESS003 Essential Thrombocythemia 70 1.467
187
P GST049 Gastrointestinal System Cancer 60 1.467
188
GST050 Gastrointestinal System Disease 56 1.467
189
BLR006 Biliary Tract Disease 52 1.467
190
BLD036 Bile Duct Disease 48 1.467
191
BLD053 Blood Platelet Disease 46 1.467
192
P ATR010 Atrial Heart Septal Defect 45 1.467
193
VRT001 Vertebral Artery Occlusion 36 1.467
194
HPT081 Hepatic Infarction 34 1.467
195
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 33 1.467
196
ALC001 Alcohol-Related Birth Defect 31 1.467
197
HMN004 Hemangioma of Liver 29 1.467
198
LWR004 Lower Urinary Tract Calculus 28 1.467
199
END074 Endocardium Disease 26 1.467
200
DSS006 Disuse Amblyopia 26 1.467
201
P RTN102 Retinitis Pigmentosa, Y-Linked 23 1.467
202
OCL010 Ocular Hypotension 38 0.077
203
VGN023 Vaginitis 42 0.063
204
FSC002 Fascioliasis 42 0.063
205
P END046 Endometritis 32 0.063
206
BYS001 Byssinosis 31 0.063
207
P CLR023 Colorectal Cancer 97 0.044
208
c SYS001 Systemic Lupus Erythematosus 86 0.044
209
P ART022 Arthritis 75 0.044
210
INS024 Insulin-Like Growth Factor I 75 0.044
211
P ADN016 Adenocarcinoma 69 0.044
212
P GLB002 Glioblastoma 68 0.044
213
P LPS004 Lupus Erythematosus 64 0.044
214
PRT037 Pertussis 64 0.044
215
P OST002 Osteoporosis 64 0.044
216
GNG013 Gingivitis 61 0.044
217
MSL001 Measles 61 0.044
218
P NPH009 Nephrolithiasis 60 0.044
219
CLT003 Colitis 60 0.044
220
END041 Endometrial Adenocarcinoma 56 0.044
221
ZLL001 Zellweger Syndrome 56 0.044
222
LYM027 Lymphopenia 56 0.044
223
ANN002 Anencephaly 54 0.044
224
P PLY014 Polycystic Kidney Disease 53 0.044
225
OLG003 Oligohydramnios 53 0.044
226
SCK005 Sickle Cell Disease 51 0.044
227
URN009 Urinary System Disease 50 0.044
228
P CLL015 Collagen Disease 50 0.044
229
OST016 Osteochondrosis 50 0.044
230
P URF003 Urofacial Syndrome 1 50 0.044
231
SLD003 Sialadenitis 49 0.044
232
ACT017 Acute Chest Syndrome 48 0.044
233
ECT026 Ectopic Pregnancy 48 0.044
234
c XNT010 Xanthinuria, Type I 47 0.044
235
GST009 Gastroschisis 47 0.044
236
PYL006 Pyloric Stenosis 46 0.044
237
ANG011 Angiodysplasia 44 0.044
238
P HYP009 Hypertrophic Pyloric Stenosis 42 0.044
239
FML031 Female Stress Incontinence 40 0.044
240
PRL008 Paralytic Ileus 37 0.044
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