Search results for "[genes] F2"

168 hits were found for '[genes] F2'

# Family MCID Name MIFTS Score
1
c THR092 Thrombophilia Due to Thrombin Defect 58 15.275
2
P HYP620 Hypoprothrombinemia 51 15.275
3
P HPT021 Hepatitis 77 14.142
4
STR067 Stroke, Ischemic 73 12.910
5
c HPT016 Hepatitis B 67 12.910
6
LVR012 Liver Cirrhosis 66 12.910
7
ALC006 Alcoholic Hepatitis 64 12.910
8
P THR014 Thrombocytopenia 62 12.910
9
P THR015 Thrombophilia 57 12.910
10
DSS009 Disseminated Intravascular Coagulation 55 12.910
11
PRG096 Pregnancy Loss, Recurrent 2 21 12.910
12
HPT023 Hepatocellular Carcinoma 90 11.547
13
P LVR013 Liver Disease 73 11.547
14
GLC006 Galactosemia 70 11.547
15
P ATR011 Atrial Fibrillation 63 11.547
16
c VRL010 Viral Hepatitis 63 11.547
17
c HMP004 Hemophilia B 62 11.547
18
c ATM011 Autoimmune Hepatitis 62 11.547
19
VNW001 Von Willebrand's Disease 62 11.547
20
P ANT006 Antiphospholipid Syndrome 61 11.547
21
P PRT013 Portal Hypertension 59 11.547
22
P PRM006 Primary Biliary Cirrhosis 58 11.547
23
PLM033 Pulmonary Embolism 57 11.547
24
PRT011 Protein C Deficiency 57 11.547
25
THR004 Thrombocytosis 56 11.547
26
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 54 11.547
27
PRT014 Protein S Deficiency 52 11.547
28
PRT018 Portal Vein Thrombosis 49 11.547
29
URT039 Urticaria 48 11.547
30
PRT012 Prothrombin Deficiency 48 11.547
31
HPT014 Hepatorenal Syndrome 47 11.547
32
P MYC007 Myocardial Infarction 80 10.000
33
WLS001 Wilson Disease 73 10.000
34
SCK003 Sickle Cell Anemia 71 10.000
35
CRB037 Cerebral Palsy 69 10.000
36
LPT001 Leptospirosis 68 10.000
37
PRT036 Peritonitis 68 10.000
38
CRB039 Cerebrovascular Disease 67 10.000
39
DNG002 Dengue Hemorrhagic Fever 67 10.000
40
TYP007 Typhoid Fever 65 10.000
41
FCT003 Factor X Deficiency 63 10.000
42
FCT007 Factor Vii Deficiency 63 10.000
43
GLN010 Glanzmann Thrombasthenia 63 10.000
44
OST003 Osteonecrosis 62 10.000
45
P ADL010 Adult Respiratory Distress Syndrome 60 10.000
46
c PRC016 Pre-Eclampsia 60 10.000
47
INT002 Intermittent Claudication 59 10.000
48
c HPT003 Hepatitis a 59 10.000
49
HPT019 Hepatic Encephalopathy 58 10.000
50
c HPT007 Hepatitis E 58 10.000
51
P ECL001 Eclampsia 57 10.000
52
INT075 Intracranial Hypertension 55 10.000
53
PTN001 Patent Foramen Ovale 55 10.000
54
FCT022 Factor Xi Deficiency, Autosomal Recessive 54 10.000
55
FCT013 Factor V Leiden Thrombophilia 54 10.000
56
CHL067 Cholecystitis 54 10.000
57
HPR003 Heparin-Induced Thrombocytopenia 53 10.000
58
VND001 Vein Disease 53 10.000
59
P END033 Endocarditis 53 10.000
60
P RTN022 Retinal Vein Occlusion 52 10.000
61
BRN082 Bernard-Soulier Syndrome, Type C 52 10.000
62
THR016 Thrombophlebitis 52 10.000
63
c AFB002 Afibrinogenemia, Congenital 52 10.000
64
PST095 Post-Thrombotic Syndrome 51 10.000
65
OBS001 Obstructive Jaundice 51 10.000
66
ALC009 Alcoholic Liver Cirrhosis 51 10.000
67
c ACT134 Acute Liver Failure 50 10.000
68
P SCK002 Sick Sinus Syndrome 50 10.000
69
HLL004 Hellp Syndrome 50 10.000
70
c CNT016 Central Retinal Vein Occlusion 49 10.000
71
PLC007 Placental Abruption 49 10.000
72
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 10.000
73
P CHL066 Cholangitis 48 10.000
74
HPT008 Hepatic Tuberculosis 47 10.000
75
P RTN014 Retinal Artery Occlusion 47 10.000
76
BLR008 Bilirubin Metabolic Disorder 46 10.000
77
HYP063 Hypersplenism 46 10.000
78
c HMG003 Hemoglobin E Disease 45 10.000
79
P CMP008 Compartment Syndrome 45 10.000
80
FCT001 Factor Viii Deficiency 45 10.000
81
ESP002 Esophageal Varix 45 10.000
82
ISC015 Ischemic Colitis 43 10.000
83
CVR006 Cavernous Hemangioma 43 10.000
84
HPT004 Hepatic Coma 43 10.000
85
CHL039 Choledocholithiasis 37 10.000
86
VTM001 Vitamin K Deficiency Hemorrhagic Disease 31 10.000
87
PRT045 Prothrombin-Related Thrombophilia 27 10.000
88
SPT005 Spotted Fever 61 8.165
89
ART111 Artery Disease 61 8.165
90
FCT006 Factor V Deficiency 60 8.165
91
PLM010 Pulmonary Edema 56 8.165
92
HNT002 Hantavirus Pulmonary Syndrome 54 8.165
93
SCT005 Scott Syndrome 52 8.165
94
P BDD001 Budd-Chiari Syndrome 52 8.165
95
VLV011 Vulvovaginal Candidiasis 52 8.165
96
RTN021 Retinal Vascular Occlusion 51 8.165
97
P DYS026 Dysfibrinogenemia 50 8.165
98
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 8.165
99
ISC002 Ischemic Optic Neuropathy 48 8.165
100
MSN003 Mesenteric Vascular Occlusion 48 8.165
101
c SVR056 Severe Hemophilia a 47 8.165
102
FRC001 Fructose-1,6-Bisphosphatase Deficiency 47 8.165
103
MTR003 Mitral Valve Stenosis 47 8.165
104
VNW005 Von Willebrand Disease, Type 1 47 8.165
105
P BLD051 Blood Coagulation Disease 46 8.165
106
P AFB001 Afibrinogenemia 46 8.165
107
P PRP034 Purpura Fulminans 46 8.165
108
ACT058 Active Peptic Ulcer Disease 48 8.165
109
HPT020 Hepatic Vascular Disease 45 8.165
110
HPT002 Hepatic Vein Thrombosis 45 8.165
111
c CHR064 Chronic Monocytic Leukemia 44 8.165
112
HRT008 Heart Conduction Disease 44 8.165
113
SDD008 Sudden Sensorineural Hearing Loss 43 8.165
114
PRP028 Peripheral Vertigo 43 8.165
115
P PRN026 Porencephaly 43 8.165
116
KRN001 Korean Hemorrhagic Fever 43 8.165
117
SPL012 Splenic Disease 43 8.165
118
THR035 Thrombasthenia 42 8.165
119
WTR001 Waterhouse-Friderichsen Syndrome 42 8.165
120
CRD001 Cardiac Tamponade 42 8.165
121
STR081 Stormorken Syndrome 41 8.165
122
BRN026 Branch Retinal Artery Occlusion 41 8.165
123
PLM013 Pulmonary Immaturity 41 8.165
124
BLD054 Blood Protein Disease 40 8.165
125
c INH004 Inherited Blood Coagulation Disease 39 8.165
126
BSL004 Basilar Artery Occlusion 39 8.165
127
HYP016 Hypochondriasis 40 8.165
128
LCH001 Leech Infestation 39 8.165
129
ABD004 Abdominal Tuberculosis 39 8.165
130
QLT001 Qualitative Platelet Defect 39 8.165
131
BLT003 Blue Toe Syndrome 38 8.165
132
PLS002 Peliosis Hepatis 38 8.165
133
SPL007 Splenic Abscess 38 8.165
134
FMR003 Femoral Neuropathy 38 8.165
135
CHL040 Cholangiolocellular Carcinoma 38 8.165
136
SBN001 Subendocardial Myocardial Infarction 38 8.165
137
ASC003 Ascending Cholangitis 37 8.165
138
INF001 Infarct of Liver 37 8.165
139
LVD002 Livedoid Vasculopathy 37 8.165
140
MRN001 Marantic Endocarditis 36 8.165
141
WND001 Wound Botulism 36 8.165
142
EPS001 Epstein-Barr Virus Hepatitis 36 8.165
143
c ACT072 Acute Laryngitis 36 8.165
144
HMC014 Homocysteinemia 35 8.165
145
GNT005 Giant Hemangioma 35 8.165
146
ANT013 Anterior Spinal Artery Syndrome 35 8.165
147
ISC001 Ischemic Neuropathy 35 8.165
148
FRN014 Fournier Gangrene 35 8.165
149
INT010 Intracranial Embolism 34 8.165
150
BND003 Binder Syndrome 34 8.165
151
ART110 Arteritic Anterior Ischemic Optic Neuropathy 34 8.165
152
INT050 Intestinal Impaction 33 8.165
153
ANT022 Anterior Cranial Fossa Meningioma 32 8.165
154
TYL001 Taylor's Syndrome 29 8.165
155
END074 Endocardium Disease 27 8.165
156
BNP002 Bone Epithelioid Hemangioma 26 8.165
157
c MLG042 Malignant Otitis Externa 26 8.165
158
c ANT010 Anterior Compartment Syndrome 24 8.165
159
HPT066 Hepatoportal Sclerosis 23 8.165
160
PHN001 Phencyclidine Abuse 23 8.165
161
CRB017 Cerebral Falx Meningioma 22 8.165
162
HLR004 Hilar Cholangiocellular Carcinoma 16 8.165
163
P GST049 Gastrointestinal System Cancer 61 5.774
164
GST050 Gastrointestinal System Disease 54 5.774
165
BLD053 Blood Platelet Disease 47 5.774
166
DSS024 Disease of Anatomical Entity 43 5.774
167
CRB132 Cerebral Sinovenous Thrombosis 32 5.774
168
CNG454 Congenital Factor Ii Deficiency 24 5.774