Search results for f2

254 hits were found for f2

# Family MCID Name MIFTS Score
1
PRT129 Prothrombin Deficiency, Congenital 51 3.250
2
STR067 Stroke, Ischemic 84 2.799
3
P THR015 Thrombophilia 58 2.773
4
PRG096 Pregnancy Loss, Recurrent 2 12 2.601
5
c THR092 Thrombophilia Due to Thrombin Defect 61 2.574
6
P LVR013 Liver Disease 76 2.526
7
LVR012 Liver Cirrhosis 73 2.306
8
c HPT016 Hepatitis B 68 2.306
9
ALC006 Alcoholic Hepatitis 62 2.306
10
THR024 Thrombosis 61 2.306
11
P HPT023 Hepatocellular Carcinoma 94 2.062
12
P HPT021 Hepatitis 75 2.062
13
c HMP004 Hemophilia B 67 2.062
14
FCT002 Factor Xi Deficiency 64 2.062
15
c ATM011 Autoimmune Hepatitis 63 2.062
16
PLM033 Pulmonary Embolism 62 2.062
17
FCT007 Factor Vii Deficiency 62 2.062
18
VNW001 Von Willebrand's Disease 61 2.062
19
P HMR003 Hemorrhagic Disease 61 2.062
20
P BRN019 Bernard-Soulier Syndrome 60 2.062
21
c VRL010 Viral Hepatitis 59 2.062
22
P PRT013 Portal Hypertension 59 2.062
23
P ANT006 Antiphospholipid Syndrome 59 2.062
24
HPT019 Hepatic Encephalopathy 59 2.062
25
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 2.062
26
ANT009 Antithrombin Iii Deficiency 58 2.062
27
FCT003 Factor X Deficiency 58 2.062
28
DSS009 Disseminated Intravascular Coagulation 56 2.062
29
THR004 Thrombocytosis 55 2.062
30
P PRM006 Primary Biliary Cirrhosis 55 2.062
31
ALC009 Alcoholic Liver Cirrhosis 53 2.062
32
c ACT134 Acute Liver Failure 52 2.062
33
PRT018 Portal Vein Thrombosis 50 2.062
34
HYP063 Hypersplenism 49 2.062
35
HPT014 Hepatorenal Syndrome 49 2.062
36
PRT011 Protein C Deficiency 48 2.062
37
PRT014 Protein S Deficiency 47 2.062
38
PRT012 Prothrombin Deficiency 46 1.830
39
c SYS001 Systemic Lupus Erythematosus 86 1.809
40
P HRT032 Heart Disease 80 1.786
41
SCK003 Sickle Cell Anemia 73 1.786
42
WLS001 Wilson Disease 72 1.786
43
PRP027 Peripheral Vascular Disease 71 1.786
44
CRB037 Cerebral Palsy 70 1.786
45
P ATR011 Atrial Fibrillation 68 1.786
46
CRB039 Cerebrovascular Disease 68 1.786
47
P ADL010 Adult Respiratory Distress Syndrome 67 1.786
48
PRT036 Peritonitis 67 1.786
49
DNG002 Dengue Hemorrhagic Fever 66 1.786
50
GLN010 Glanzmann Thrombasthenia 66 1.786
51
c PRC016 Pre-Eclampsia 65 1.786
52
LPT001 Leptospirosis 64 1.786
53
VRC005 Varicose Veins 64 1.786
54
c HPT003 Hepatitis a 63 1.786
55
OST003 Osteonecrosis 63 1.786
56
BRG013 Buerger Disease 62 1.786
57
SCH014 Schistosomiasis 62 1.786
58
PRP030 Purpura 61 1.786
59
INT002 Intermittent Claudication 61 1.786
60
c AFB002 Afibrinogenemia, Congenital 61 1.786
61
CHL068 Cholestasis 60 1.786
62
PLC005 Placental Insufficiency 59 1.786
63
CHL067 Cholecystitis 58 1.786
64
PTN001 Patent Foramen Ovale 58 1.786
65
BDD001 Budd-Chiari Syndrome 58 1.786
66
P END033 Endocarditis 58 1.786
67
P ECL001 Eclampsia 57 1.786
68
c HPT007 Hepatitis E 57 1.786
69
PLM010 Pulmonary Edema 57 1.786
70
SPT005 Spotted Fever 57 1.786
71
INF034 Infective Endocarditis 56 1.786
72
P SCK002 Sick Sinus Syndrome 53 1.786
73
P VNS003 Venous Insufficiency 53 1.786
74
P RTN022 Retinal Vein Occlusion 53 1.786
75
INT075 Intracranial Hypertension 53 1.786
76
P OBS001 Obstructive Jaundice 53 1.786
77
HLL004 Hellp Syndrome 53 1.786
78
THR016 Thrombophlebitis 53 1.786
79
PST095 Post-Thrombotic Syndrome 52 1.786
80
c HPT015 Hepatitis D 52 1.786
81
P CHL066 Cholangitis 52 1.786
82
FCT006 Factor V Deficiency 52 1.786
83
FCT001 Factor Viii Deficiency 50 1.786
84
PLC007 Placental Abruption 50 1.786
85
c CNT016 Central Retinal Vein Occlusion 50 1.786
86
PPL021 Papilledema 50 1.786
87
HMC014 Homocysteinemia 49 1.786
88
SND002 Sneddon Syndrome 48 1.786
89
VND001 Vein Disease 48 1.786
90
CVR006 Cavernous Hemangioma 48 1.786
91
SCT005 Scott Syndrome 48 1.786
92
P CMP008 Compartment Syndrome 48 1.786
93
ESP002 Esophageal Varix 46 1.786
94
P RTN014 Retinal Artery Occlusion 45 1.786
95
BLR008 Bilirubin Metabolic Disorder 45 1.786
96
P PRP034 Purpura Fulminans 44 1.786
97
HPT004 Hepatic Coma 40 1.786
98
ISC015 Ischemic Colitis 39 1.786
99
CHL039 Choledocholithiasis 38 1.786
100
HPT008 Hepatic Tuberculosis 37 1.786
101
VTM001 Vitamin K Deficiency Hemorrhagic Disease 35 1.786
102
c HMG003 Hemoglobin E Disease 34 1.786
103
SGT001 Sagittal Sinus Thrombosis 34 1.786
104
P MYC007 Myocardial Infarction 81 1.458
105
P ESS003 Essential Thrombocythemia 71 1.458
106
P HMP007 Hemophilia 61 1.458
107
P HMR012 Hemorrhagic Fever 60 1.458
108
IMM136 Immune System Disease 57 1.458
109
HNT002 Hantavirus Pulmonary Syndrome 57 1.458
110
NNL002 Nonalcoholic Steatohepatitis 56 1.458
111
P DYS026 Dysfibrinogenemia 51 1.458
112
P PRN026 Porencephaly 50 1.458
113
P AFB001 Afibrinogenemia 49 1.458
114
STR081 Stormorken Syndrome 49 1.458
115
ISC002 Ischemic Optic Neuropathy 48 1.458
116
VNW005 Von Willebrand Disease, Type 1 47 1.458
117
c THR082 Thrombophilia Due to Activated Protein C Resistance 47 1.458
118
SDD008 Sudden Sensorineural Hearing Loss 46 1.458
119
c SVR056 Severe Hemophilia a 46 1.458
120
THR035 Thrombasthenia 46 1.458
121
RTN021 Retinal Vascular Occlusion 45 1.458
122
BLD053 Blood Platelet Disease 45 1.458
123
CRD001 Cardiac Tamponade 45 1.458
124
P ANL018 Analbuminemia 45 1.458
125
P ATR010 Atrial Heart Septal Defect 45 1.458
126
ACT058 Active Peptic Ulcer Disease 43 1.458
127
MRB001 Marburg Hemorrhagic Fever 43 1.458
128
LCH001 Leech Infestation 43 1.458
129
KWS001 Kwashiorkor 43 1.458
130
SPL012 Splenic Disease 42 1.458
131
HYP016 Hypochondriasis 42 1.458
132
KRN001 Korean Hemorrhagic Fever 42 1.458
133
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 40 1.458
134
FMR003 Femoral Neuropathy 39 1.458
135
SQM002 Squamous Cell Papilloma 39 1.458
136
MXL016 Maxillonasal Dysplasia, Binder Type 39 1.458
137
FRN014 Fournier Gangrene 38 1.458
138
INT010 Intracranial Embolism 38 1.458
139
P BLD051 Blood Coagulation Disease 38 1.458
140
BLT003 Blue Toe Syndrome 38 1.458
141
PRP028 Peripheral Vertigo 37 1.458
142
MRN001 Marantic Endocarditis 37 1.458
143
HPT020 Hepatic Vascular Disease 36 1.458
144
VSC008 Vascular Hemostatic Disease 36 1.458
145
ENT001 Enterocele 36 1.458
146
HYP737 Hyperhidrosis, Gustatory 36 1.458
147
LVD002 Livedoid Vasculopathy 36 1.458
148
PLS002 Peliosis Hepatis 36 1.458
149
BRN026 Branch Retinal Artery Occlusion 35 1.458
150
CNR001 Coenurosis 35 1.458
151
BSL004 Basilar Artery Occlusion 35 1.458
152
CRY036 Cryptogenic Cirrhosis 34 1.458
153
SPL006 Splenic Infarction 34 1.458
154
c CHR064 Chronic Monocytic Leukemia 34 1.458
155
MSN003 Mesenteric Vascular Occlusion 33 1.458
156
GNT005 Giant Hemangioma 33 1.458
157
TYL001 Taylor's Syndrome 33 1.458
158
ANT013 Anterior Spinal Artery Syndrome 33 1.458
159
SPN185 Spinal Cord Infarction 33 1.458
160
ASC003 Ascending Cholangitis 33 1.458
161
QLT001 Qualitative Platelet Defect 32 1.458
162
EXH001 Exhibitionism 32 1.458
163
HRT008 Heart Conduction Disease 32 1.458
164
ANT022 Anterior Cranial Fossa Meningioma 32 1.458
165
ALC001 Alcohol-Related Birth Defect 32 1.458
166
ABD004 Abdominal Tuberculosis 31 1.458
167
SBN001 Subendocardial Myocardial Infarction 31 1.458
168
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 1.458
169
SPR011 Suprasellar Meningioma 30 1.458
170
ISC005 Ischemic Bone Disease 30 1.458
171
URT011 Urethral Calculus 30 1.458
172
PRC051 Paracetamol Poisoning 30 1.458
173
HMN004 Hemangioma of Liver 30 1.458
174
HPT081 Hepatic Infarction 30 1.458
175
EPS001 Epstein-Barr Virus Hepatitis 29 1.458
176
c INH004 Inherited Blood Coagulation Disease 29 1.458
177
PRM008 Parametritis 29 1.458
178
END013 Endometrial Small Cell Carcinoma 28 1.458
179
c MLG042 Malignant Otitis Externa 28 1.458
180
ORB007 Orbital Cyst 28 1.458
181
INT050 Intestinal Impaction 27 1.458
182
ISC001 Ischemic Neuropathy 26 1.458
183
P RTN102 Retinitis Pigmentosa, Y-Linked 26 1.458
184
ECC005 Eccrine Adenocarcinoma 25 1.458
185
BLD054 Blood Protein Disease 25 1.458
186
c ANT010 Anterior Compartment Syndrome 25 1.458
187
CRB017 Cerebral Falx Meningioma 25 1.458
188
PHN001 Phencyclidine Abuse 24 1.458
189
NNH002 Non-a-E Hepatitis 23 1.458
190
LWR004 Lower Urinary Tract Calculus 22 1.458
191
ANT078 Antipyrine Metabolism 22 1.458
192
END074 Endocardium Disease 22 1.458
193
PRL015 Prolapse of Female Genital Organ 21 1.458
194
LMB003 Lumbosacral Lipoma 21 1.458
195
HPT066 Hepatoportal Sclerosis 20 1.458
196
HLR004 Hilar Cholangiocellular Carcinoma 12 1.458
197
URT015 Urethral False Passage 11 1.458
198
MDD001 Middle Cranial Fossa Meningioma 10 1.458
199
CRB132 Cerebral Sinovenous Thrombosis 32 1.067
200
GST050 Gastrointestinal System Disease 66 1.031
201
P GST049 Gastrointestinal System Cancer 60 1.031
202
BLR006 Biliary Tract Disease 55 1.031
203
BLD036 Bile Duct Disease 52 1.031
204
ART140 Arteries, Anomalies of 51 1.031
205
OCL010 Ocular Hypotension 39 0.075
206
c BLD140 Blood Group, I System 37 0.075
207
VGN023 Vaginitis 59 0.062
208
P END046 Endometritis 51 0.062
209
FSC002 Fascioliasis 45 0.062
210
BYS001 Byssinosis 33 0.062
211
P CLR023 Colorectal Cancer 98 0.044
212
INS024 Insulin-Like Growth Factor I 83 0.044
213
P ART022 Arthritis 77 0.044
214
P OST002 Osteoporosis 75 0.044
215
GLB002 Glioblastoma 74 0.044
216
P DBT009 Diabetes Mellitus 72 0.044
217
P ADN016 Adenocarcinoma 71 0.044
218
PRT037 Pertussis 70 0.044
219
P LPS004 Lupus Erythematosus 69 0.044
220
MSL001 Measles 64 0.044
221
GNG013 Gingivitis 64 0.044
222
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.044
223
CLT003 Colitis 63 0.044
224
P PLY014 Polycystic Kidney Disease 60 0.044
225
GT001 Gout 60 0.044
226
P INF032 Infertility 59 0.044
227
END041 Endometrial Adenocarcinoma 59 0.044
228
URN009 Urinary System Disease 58 0.044
229
ANN002 Anencephaly 57 0.044
230
NPH009 Nephrolithiasis 57 0.044
231
P ZLL001 Zellweger Syndrome 56 0.044
232
LYM027 Lymphopenia 56 0.044
233
GST009 Gastroschisis 55 0.044
234
SCK005 Sickle Cell Disease 54 0.044
235
P CLL015 Collagen Disease 53 0.044
236
OST016 Osteochondrosis 52 0.044
237
ECT026 Ectopic Pregnancy 52 0.044
238
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.044
239
ACT017 Acute Chest Syndrome 50 0.044
240
SLD003 Sialadenitis 49 0.044
241
ANV001 Anovulation 48 0.044
242
ANG011 Angiodysplasia 48 0.044
243
PYL006 Pyloric Stenosis 47 0.044
244
P HYP009 Hypertrophic Pyloric Stenosis 45 0.044
245
OLG003 Oligohydramnios 41 0.044
246
FML031 Female Stress Incontinence 40 0.044
247
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.044
248
PRL008 Paralytic Ileus 38 0.044
249
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.044
250
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.044
251
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.044
252
P STR035 Streptococcal Group a Invasive Disease 28 0.044
253
c INH005 Inherited Hypoprothrombinemia 14 0.044
254
PRT045 Prothrombin-Related Thrombophilia 12 0.044
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