Search results for "[genes] F2"

205 hits were found for '[genes] F2'

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 50 15.668
2
c THR092 Thrombophilia Due to Thrombin Defect 56 14.656
3
STR067 Stroke, Ischemic 74 12.387
4
PRG096 Pregnancy Loss, Recurrent 2 22 12.387
5
HPT023 Hepatocellular Carcinoma 90 11.079
6
FCT007 Factor Vii Deficiency 60 11.079
7
FCT003 Factor X Deficiency 62 11.079
8
c HMP004 Hemophilia B 61 11.079
9
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 11.079
10
P THR015 Thrombophilia 59 11.079
11
PRT012 Prothrombin Deficiency 43 11.079
12
c SYS001 Systemic Lupus Erythematosus 87 9.595
13
WLS001 Wilson Disease 72 9.595
14
SCK003 Sickle Cell Anemia 72 9.595
15
P RSP003 Respiratory Failure 68 9.595
16
BRN082 Bernard-Soulier Syndrome, Type C 51 9.595
17
GLN010 Glanzmann Thrombasthenia 64 9.595
18
PLM033 Pulmonary Embolism 59 9.595
19
CRB037 Cerebral Palsy 54 9.595
20
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 9.595
21
FCT022 Factor Xi Deficiency, Autosomal Recessive 55 9.595
22
FCT006 Factor V Deficiency 62 9.595
23
LPT001 Leptospirosis 65 9.595
24
SND002 Sneddon Syndrome 45 9.595
25
CRB039 Cerebrovascular Disease 49 9.595
26
CHL067 Cholecystitis 57 9.595
27
BRG013 Buerger Disease 54 9.595
28
THR016 Thrombophlebitis 55 9.595
29
PRP027 Peripheral Vascular Disease 69 9.595
30
PRT036 Peritonitis 65 9.595
31
LVR012 Liver Cirrhosis 71 9.595
32
SCT005 Scott Syndrome 51 9.595
33
PPL021 Papilledema 47 9.595
34
c HPT015 Hepatitis D 51 9.595
35
SCH014 Schistosomiasis 59 9.595
36
TYP007 Typhoid Fever 61 9.595
37
VSC007 Vascular Disease 51 9.595
38
P ADL010 Adult Respiratory Distress Syndrome 60 9.595
39
P ECL001 Eclampsia 55 9.595
40
PRP030 Purpura 60 9.595
41
c HPT003 Hepatitis a 55 9.595
42
SPT005 Spotted Fever 56 9.595
43
PTN001 Patent Foramen Ovale 55 9.595
44
P PRT013 Portal Hypertension 61 9.595
45
P ANT006 Antiphospholipid Syndrome 60 9.595
46
c ATM011 Autoimmune Hepatitis 62 9.595
47
HPT019 Hepatic Encephalopathy 58 9.595
48
PRT014 Protein S Deficiency 54 9.595
49
P PRM006 Primary Biliary Cirrhosis 55 9.595
50
OST003 Osteonecrosis 45 9.595
51
P VNS003 Venous Insufficiency 53 9.595
52
BLR001 Biliary Atresia 52 9.595
53
c VRL010 Viral Hepatitis 60 9.595
54
PLM010 Pulmonary Edema 56 9.595
55
CVR006 Cavernous Hemangioma 46 9.595
56
DSS009 Disseminated Intravascular Coagulation 52 9.595
57
INT002 Intermittent Claudication 56 9.595
58
INT075 Intracranial Hypertension 52 9.595
59
THR004 Thrombocytosis 55 9.595
60
c HMG003 Hemoglobin E Disease 44 9.595
61
VND001 Vein Disease 51 9.595
62
HPT014 Hepatorenal Syndrome 47 9.595
63
DNG002 Dengue Hemorrhagic Fever 60 9.595
64
P CMP008 Compartment Syndrome 46 9.595
65
FCT001 Factor Viii Deficiency 41 9.595
66
c HPT007 Hepatitis E 51 9.595
67
PST095 Post-Thrombotic Syndrome 48 9.595
68
HPT008 Hepatic Tuberculosis 42 9.595
69
HLL004 Hellp Syndrome 48 9.595
70
c PRT045 Prothrombin-Related Thrombophilia 25 9.595
71
PLC007 Placental Abruption 46 9.595
72
PRT011 Protein C Deficiency 52 9.595
73
OBS001 Obstructive Jaundice 47 9.595
74
INF034 Infective Endocarditis 50 9.595
75
ALC009 Alcoholic Liver Cirrhosis 53 9.595
76
HYP063 Hypersplenism 49 9.595
77
P END033 Endocarditis 52 9.595
78
HYP037 Hyperhomocysteinemia 49 9.595
79
ALC006 Alcoholic Hepatitis 60 9.595
80
PRT018 Portal Vein Thrombosis 48 9.595
81
P PRP034 Purpura Fulminans 41 9.595
82
ISC015 Ischemic Colitis 38 9.595
83
P CHL066 Cholangitis 48 9.595
84
PLC005 Placental Insufficiency 50 9.595
85
c CNT016 Central Retinal Vein Occlusion 34 9.595
86
SGT001 Sagittal Sinus Thrombosis 32 9.595
87
P RTN014 Retinal Artery Occlusion 32 9.595
88
P RTN022 Retinal Vein Occlusion 36 9.595
89
CHL039 Choledocholithiasis 32 9.595
90
LMB062 Limb Ischemia 48 9.595
91
P MYC007 Myocardial Infarction 80 7.834
92
P ESS003 Essential Thrombocythemia 66 7.834
93
GST050 Gastrointestinal System Disease 58 7.834
94
c AFB002 Afibrinogenemia, Congenital 51 7.834
95
P BDD001 Budd-Chiari Syndrome 52 7.834
96
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 7.834
97
VNW007 Von Willebrand Disease 57 7.834
98
NTR005 Nutritional Deficiency Disease 51 7.834
99
STR081 Stormorken Syndrome 50 7.834
100
BLR008 Bilirubin Metabolic Disorder 46 7.834
101
HNT002 Hantavirus Pulmonary Syndrome 51 7.834
102
FRC001 Fructose-1,6-Bisphosphatase Deficiency 41 7.834
103
P INT001 Intrahepatic Cholestasis 58 7.834
104
VNW005 Von Willebrand Disease, Type 1 48 7.834
105
SPL012 Splenic Disease 48 7.834
106
MRB001 Marburg Hemorrhagic Fever 41 7.834
107
ESP002 Esophageal Varix 43 7.834
108
P HMP007 Hemophilia 55 7.834
109
c PRC016 Pre-Eclampsia 57 7.834
110
MTR003 Mitral Valve Stenosis 40 7.834
111
HRT008 Heart Conduction Disease 43 7.834
112
ACT058 Active Peptic Ulcer Disease 44 7.834
113
VLV011 Vulvovaginal Candidiasis 47 7.834
114
P HRT032 Heart Disease 64 7.834
115
FRY001 Frey Syndrome 38 7.834
116
P SCK002 Sick Sinus Syndrome 49 7.834
117
HYP016 Hypochondriasis 39 7.834
118
FCT005 Factor Xiii Deficiency 42 7.834
119
P PRN026 Porencephaly 47 7.834
120
MXL016 Maxillonasal Dysplasia, Binder Type 29 7.834
121
KWS001 Kwashiorkor 45 7.834
122
c ACT071 Acute Kidney Failure 48 7.834
123
SCK005 Sickle Cell Disease 51 7.834
124
BLD036 Bile Duct Disease 47 7.834
125
RTN021 Retinal Vascular Occlusion 33 7.834
126
LVD002 Livedoid Vasculopathy 33 7.834
127
c ACT134 Acute Liver Failure 46 7.834
128
TYL001 Taylor's Syndrome 28 7.834
129
ENT001 Enterocele 39 7.834
130
LWR004 Lower Urinary Tract Calculus 30 7.834
131
KRN001 Korean Hemorrhagic Fever 39 7.834
132
FMR003 Femoral Neuropathy 34 7.834
133
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 7.834
134
BLD053 Blood Platelet Disease 44 7.834
135
QLT001 Qualitative Platelet Defect 30 7.834
136
CRD001 Cardiac Tamponade 43 7.834
137
ANT013 Anterior Spinal Artery Syndrome 27 7.834
138
c ACT075 Acute Myocardial Infarction 61 7.834
139
HPT004 Hepatic Coma 39 7.834
140
SDD008 Sudden Sensorineural Hearing Loss 30 7.834
141
URT011 Urethral Calculus 28 7.834
142
PRP028 Peripheral Vertigo 42 7.834
143
PLS002 Peliosis Hepatis 32 7.834
144
WND001 Wound Botulism 31 7.834
145
BRN026 Branch Retinal Artery Occlusion 37 7.834
146
ART111 Artery Disease 56 7.834
147
LCH001 Leech Infestation 35 7.834
148
EXH001 Exhibitionism 31 7.834
149
CRB017 Cerebral Falx Meningioma 18 7.834
150
EPS001 Epstein-Barr Virus Hepatitis 28 7.834
151
HPT020 Hepatic Vascular Disease 43 7.834
152
P BLD051 Blood Coagulation Disease 44 7.834
153
BNP002 Bone Epithelioid Hemangioma 18 7.834
154
VRT001 Vertebral Artery Occlusion 35 7.834
155
SRC011 Sarcocystosis 35 7.834
156
c ACT072 Acute Laryngitis 37 7.834
157
HPT002 Hepatic Vein Thrombosis 38 7.834
158
ANT022 Anterior Cranial Fossa Meningioma 26 7.834
159
END074 Endocardium Disease 26 7.834
160
ABD004 Abdominal Tuberculosis 37 7.834
161
c CHR064 Chronic Monocytic Leukemia 42 7.834
162
INT010 Intracranial Embolism 32 7.834
163
c MLG042 Malignant Otitis Externa 27 7.834
164
NNH002 Non-a-E Hepatitis 21 7.834
165
DSS006 Disuse Amblyopia 19 7.834
166
FRN014 Fournier Gangrene 33 7.834
167
HLR004 Hilar Cholangiocellular Carcinoma 13 7.834
168
MRN001 Marantic Endocarditis 34 7.834
169
SPN185 Spinal Cord Infarction 36 7.834
170
BLD054 Blood Protein Disease 38 7.834
171
CHL040 Cholangiolocellular Carcinoma 35 7.834
172
c INH004 Inherited Blood Coagulation Disease 38 7.834
173
PHN001 Phencyclidine Abuse 21 7.834
174
PRM008 Parametritis 28 7.834
175
SPR011 Suprasellar Meningioma 28 7.834
176
c SVR056 Severe Hemophilia a 44 7.834
177
VSC008 Vascular Hemostatic Disease 30 7.834
178
ASC003 Ascending Cholangitis 28 7.834
179
GRN009 Granulomatous Hepatitis 37 7.834
180
CNR001 Coenurosis 24 7.834
181
BLT003 Blue Toe Syndrome 33 7.834
182
ISC001 Ischemic Neuropathy 33 7.834
183
MSN003 Mesenteric Vascular Occlusion 34 7.834
184
INT050 Intestinal Impaction 28 7.834
185
ECC005 Eccrine Adenocarcinoma 25 7.834
186
c ANT010 Anterior Compartment Syndrome 21 7.834
187
BSL004 Basilar Artery Occlusion 31 7.834
188
HPT066 Hepatoportal Sclerosis 21 7.834
189
ISC005 Ischemic Bone Disease 38 7.834
190
PRL015 Prolapse of Female Genital Organ 20 7.834
191
SPL007 Splenic Abscess 35 7.834
192
URT015 Urethral False Passage 11 7.834
193
P GNT005 Giant Hemangioma 34 7.834
194
END013 Endometrial Small Cell Carcinoma 36 7.834
195
SBN001 Subendocardial Myocardial Infarction 33 7.834
196
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 7.834
197
ATM018 Autoimmune Disease of Urogenital Tract 26 7.834
198
ISC002 Ischemic Optic Neuropathy 45 7.834
199
HMC014 Homocysteinemia 32 7.834
200
THR035 Thrombasthenia 41 7.834
201
P GST049 Gastrointestinal System Cancer 59 5.539
202
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 5.539
203
BLR006 Biliary Tract Disease 50 5.539
204
CRB132 Cerebral Sinovenous Thrombosis 30 5.539
205
DSS024 Disease of Anatomical Entity 40 5.539