Search results for "[genes] F2"

168 hits were found for '[genes] F2'

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