Search results for "[genes] F2"

178 hits were found for '[genes] F2'

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 52 15.112
2
P THR015 Thrombophilia 52 15.112
3
c THR092 Thrombophilia Due to Thrombin Defect 49 13.991
4
STR067 Stroke, Ischemic 68 12.772
5
c HPT016 Hepatitis B 59 12.772
6
LVR012 Liver Cirrhosis 59 12.772
7
P HPT021 Hepatitis 58 12.772
8
ALC006 Alcoholic Hepatitis 53 12.772
9
PRT012 Prothrombin Deficiency 43 12.772
10
PRG096 Pregnancy Loss, Recurrent 2 13 12.772
11
HPT023 Hepatocellular Carcinoma 90 11.424
12
GLC006 Galactosemia 76 11.424
13
FCT007 Factor Vii Deficiency 66 11.424
14
c HMP004 Hemophilia B 65 11.424
15
VNW001 Von Willebrand's Disease 63 11.424
16
FCT003 Factor X Deficiency 58 11.424
17
P PRM006 Primary Biliary Cirrhosis 56 11.424
18
P ANT006 Antiphospholipid Syndrome 55 11.424
19
P ATR011 Atrial Fibrillation 55 11.424
20
c ATM011 Autoimmune Hepatitis 53 11.424
21
PLM033 Pulmonary Embolism 53 11.424
22
HPT019 Hepatic Encephalopathy 50 11.424
23
c VRL010 Viral Hepatitis 49 11.424
24
THR004 Thrombocytosis 48 11.424
25
DSS009 Disseminated Intravascular Coagulation 48 11.424
26
PRT011 Protein C Deficiency 46 11.424
27
PRT014 Protein S Deficiency 46 11.424
28
P PRT013 Portal Hypertension 45 11.424
29
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 44 11.424
30
ALC009 Alcoholic Liver Cirrhosis 41 11.424
31
PRT018 Portal Vein Thrombosis 41 11.424
32
HYP063 Hypersplenism 40 11.424
33
HPT014 Hepatorenal Syndrome 39 11.424
34
c SYS001 Systemic Lupus Erythematosus 90 9.893
35
SCK003 Sickle Cell Anemia 71 9.893
36
GLN010 Glanzmann Thrombasthenia 65 9.893
37
PRP027 Peripheral Vascular Disease 62 9.893
38
TYP007 Typhoid Fever 59 9.893
39
PRT036 Peritonitis 58 9.893
40
CRB039 Cerebrovascular Disease 58 9.893
41
P ADL010 Adult Respiratory Distress Syndrome 55 9.893
42
DNG002 Dengue Hemorrhagic Fever 55 9.893
43
LPT001 Leptospirosis 55 9.893
44
SCH014 Schistosomiasis 55 9.893
45
FCT006 Factor V Deficiency 54 9.893
46
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 53 9.893
47
CHL067 Cholecystitis 51 9.893
48
BRN082 Bernard-Soulier Syndrome, Type C 51 9.893
49
OST003 Osteonecrosis 50 9.893
50
P THR014 Thrombocytopenia 50 9.893
51
c HPT015 Hepatitis D 48 9.893
52
INT002 Intermittent Claudication 48 9.893
53
PTN001 Patent Foramen Ovale 48 9.893
54
THR016 Thrombophlebitis 48 9.893
55
PRP030 Purpura 47 9.893
56
FCT022 Factor Xi Deficiency, Autosomal Recessive 47 9.893
57
c HPT003 Hepatitis a 47 9.893
58
P ECL001 Eclampsia 47 9.893
59
INT075 Intracranial Hypertension 46 9.893
60
CHL068 Cholestasis 45 9.893
61
P RTN022 Retinal Vein Occlusion 45 9.893
62
PLM010 Pulmonary Edema 45 9.893
63
P VNS003 Venous Insufficiency 44 9.893
64
c ACT134 Acute Liver Failure 44 9.893
65
FCT013 Factor V Leiden Thrombophilia 43 9.893
66
SCT005 Scott Syndrome 43 9.893
67
P END033 Endocarditis 43 9.893
68
CVR006 Cavernous Hemangioma 43 9.893
69
PLC005 Placental Insufficiency 43 9.893
70
PSD002 Pseudotumor Cerebri 42 9.893
71
c HPT007 Hepatitis E 42 9.893
72
HLL004 Hellp Syndrome 42 9.893
73
INF034 Infective Endocarditis 42 9.893
74
P SCK002 Sick Sinus Syndrome 42 9.893
75
OBS001 Obstructive Jaundice 40 9.893
76
c CNT016 Central Retinal Vein Occlusion 40 9.893
77
PLC007 Placental Abruption 40 9.893
78
P CHL066 Cholangitis 39 9.893
79
PPL021 Papilledema 38 9.893
80
LMB062 Limb Ischemia 38 9.893
81
PST095 Post-Thrombotic Syndrome 38 9.893
82
P RTN014 Retinal Artery Occlusion 38 9.893
83
HPT008 Hepatic Tuberculosis 37 9.893
84
P CMP008 Compartment Syndrome 36 9.893
85
c HMG003 Hemoglobin E Disease 35 9.893
86
VND001 Vein Disease 34 9.893
87
ISC015 Ischemic Colitis 33 9.893
88
HPT004 Hepatic Coma 32 9.893
89
SGT001 Sagittal Sinus Thrombosis 32 9.893
90
P BLD051 Blood Coagulation Disease 30 9.893
91
ESP002 Esophageal Varix 30 9.893
92
CHL039 Choledocholithiasis 30 9.893
93
BLR008 Bilirubin Metabolic Disorder 30 9.893
94
VTM001 Vitamin K Deficiency Hemorrhagic Disease 29 9.893
95
c PRT045 Prothrombin-Related Thrombophilia 23 9.893
96
P MYC007 Myocardial Infarction 76 8.078
97
c HYP595 Hypertension, Essential 68 8.078
98
P RSP003 Respiratory Failure 58 8.078
99
P BDD001 Budd-Chiari Syndrome 56 8.078
100
CRB037 Cerebral Palsy 54 8.078
101
HNT002 Hantavirus Pulmonary Syndrome 52 8.078
102
P HMP007 Hemophilia 51 8.078
103
c PRC016 Pre-Eclampsia 51 8.078
104
VLV011 Vulvovaginal Candidiasis 51 8.078
105
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 8.078
106
SPT005 Spotted Fever 49 8.078
107
c AFB002 Afibrinogenemia, Congenital 46 8.078
108
P DYS026 Dysfibrinogenemia 45 8.078
109
P HMR012 Hemorrhagic Fever 44 8.078
110
GST009 Gastroschisis 43 8.078
111
P PRN026 Porencephaly 42 8.078
112
FRC001 Fructose-1,6-Bisphosphatase Deficiency 41 8.078
113
P AFB001 Afibrinogenemia 41 8.078
114
VNW005 Von Willebrand Disease, Type 1 41 8.078
115
CRD001 Cardiac Tamponade 39 8.078
116
ISC002 Ischemic Optic Neuropathy 38 8.078
117
MTR003 Mitral Valve Stenosis 38 8.078
118
RTN021 Retinal Vascular Occlusion 38 8.078
119
KWS001 Kwashiorkor 37 8.078
120
SPL012 Splenic Disease 37 8.078
121
c SVR056 Severe Hemophilia a 37 8.078
122
PLS002 Peliosis Hepatis 36 8.078
123
MDT001 Mediterranean Spotted Fever 36 8.078
124
THR035 Thrombasthenia 36 8.078
125
KRN001 Korean Hemorrhagic Fever 35 8.078
126
SPL006 Splenic Infarction 35 8.078
127
MSN003 Mesenteric Vascular Occlusion 35 8.078
128
SPL007 Splenic Abscess 34 8.078
129
VRT001 Vertebral Artery Occlusion 33 8.078
130
BRN026 Branch Retinal Artery Occlusion 33 8.078
131
HYP016 Hypochondriasis 33 8.078
132
ABD004 Abdominal Tuberculosis 33 8.078
133
HPT020 Hepatic Vascular Disease 33 8.078
134
MRN001 Marantic Endocarditis 33 8.078
135
WND001 Wound Botulism 32 8.078
136
HMC014 Homocysteinemia 32 8.078
137
HPT002 Hepatic Vein Thrombosis 32 8.078
138
ASC003 Ascending Cholangitis 32 8.078
139
LVD002 Livedoid Vasculopathy 32 8.078
140
EXH001 Exhibitionism 31 8.078
141
CHL040 Cholangiolocellular Carcinoma 31 8.078
142
BSL004 Basilar Artery Occlusion 31 8.078
143
BLT003 Blue Toe Syndrome 31 8.078
144
PRP028 Peripheral Vertigo 31 8.078
145
EPS001 Epstein-Barr Virus Hepatitis 30 8.078
146
PRM014 Periampullary Adenocarcinoma 30 8.078
147
c ACT072 Acute Laryngitis 30 8.078
148
QLT001 Qualitative Platelet Defect 30 8.078
149
FMR003 Femoral Neuropathy 30 8.078
150
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 8.078
151
FRN014 Fournier Gangrene 29 8.078
152
SPN185 Spinal Cord Infarction 29 8.078
153
GNT005 Giant Hemangioma 29 8.078
154
CRR001 Carrion's Disease 29 8.078
155
LCH001 Leech Infestation 29 8.078
156
SBN001 Subendocardial Myocardial Infarction 28 8.078
157
ISC001 Ischemic Neuropathy 28 8.078
158
ANT013 Anterior Spinal Artery Syndrome 28 8.078
159
INF001 Infarct of Liver 27 8.078
160
P ANT022 Anterior Cranial Fossa Meningioma 25 8.078
161
END074 Endocardium Disease 24 8.078
162
BND003 Binder Syndrome 24 8.078
163
c MLG042 Malignant Otitis Externa 23 8.078
164
INT010 Intracranial Embolism 23 8.078
165
INT050 Intestinal Impaction 22 8.078
166
BNP002 Bone Epithelioid Hemangioma 22 8.078
167
ACT058 Active Peptic Ulcer Disease 22 8.078
168
c ANT010 Anterior Compartment Syndrome 22 8.078
169
HPT066 Hepatoportal Sclerosis 21 8.078
170
NNH002 Non-a-E Hepatitis 20 8.078
171
PHN001 Phencyclidine Abuse 19 8.078
172
TYL001 Taylor's Syndrome 16 8.078
173
CRB017 Cerebral Falx Meningioma 16 8.078
174
CNG454 Congenital Factor Ii Deficiency 13 8.078
175
HLR004 Hilar Cholangiocellular Carcinoma 7 8.078
176
P GST049 Gastrointestinal System Cancer 43 5.712
177
BLD053 Blood Platelet Disease 32 5.712
178
CRB132 Cerebral Sinovenous Thrombosis 30 5.712