Search results for "[genes] F2"

191 hits were found for '[genes] F2'

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 54 17.733
2
STR067 Stroke, Ischemic 77 14.836
3
c THR092 Thrombophilia Due to Thrombin Defect 56 14.836
4
P LVR013 Liver Disease 72 13.736
5
P THR015 Thrombophilia 59 13.736
6
P HPT021 Hepatitis 70 12.539
7
LVR012 Liver Cirrhosis 67 12.539
8
c HPT016 Hepatitis B 64 12.539
9
ALC006 Alcoholic Hepatitis 59 12.539
10
PRG096 Pregnancy Loss, Recurrent 2 23 12.539
11
HPT023 Hepatocellular Carcinoma 91 11.215
12
c HMP029 Hemophilia a 64 11.215
13
c HMP004 Hemophilia B 62 11.215
14
FCT003 Factor X Deficiency 62 11.215
15
FCT007 Factor Vii Deficiency 62 11.215
16
c VRL010 Viral Hepatitis 61 11.215
17
VNW001 Von Willebrand's Disease 61 11.215
18
PLM033 Pulmonary Embolism 59 11.215
19
P PRT013 Portal Hypertension 59 11.215
20
P ANT006 Antiphospholipid Syndrome 58 11.215
21
c ATM011 Autoimmune Hepatitis 58 11.215
22
HPT019 Hepatic Encephalopathy 56 11.215
23
THR004 Thrombocytosis 55 11.215
24
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 11.215
25
PRT014 Protein S Deficiency 52 11.215
26
P PRM006 Primary Biliary Cirrhosis 52 11.215
27
PRT011 Protein C Deficiency 51 11.215
28
DSS009 Disseminated Intravascular Coagulation 51 11.215
29
PRT018 Portal Vein Thrombosis 49 11.215
30
ALC009 Alcoholic Liver Cirrhosis 48 11.215
31
HYP063 Hypersplenism 48 11.215
32
HPT014 Hepatorenal Syndrome 46 11.215
33
PRP027 Peripheral Vascular Disease 69 9.713
34
SCK003 Sickle Cell Anemia 68 9.713
35
P ATR011 Atrial Fibrillation 64 9.713
36
P THR014 Thrombocytopenia 64 9.713
37
GLN010 Glanzmann Thrombasthenia 63 9.713
38
LPT001 Leptospirosis 63 9.713
39
DNG002 Dengue Hemorrhagic Fever 62 9.713
40
PRT036 Peritonitis 62 9.713
41
P ADL010 Adult Respiratory Distress Syndrome 60 9.713
42
FCT006 Factor V Deficiency 60 9.713
43
c HPT003 Hepatitis a 59 9.713
44
PRP030 Purpura 59 9.713
45
SCH014 Schistosomiasis 58 9.713
46
CHL068 Cholestasis 58 9.713
47
P HMR003 Hemorrhagic Disease 57 9.713
48
SPT005 Spotted Fever 56 9.713
49
CHL067 Cholecystitis 56 9.713
50
P BDD001 Budd-Chiari Syndrome 56 9.713
51
PLM010 Pulmonary Edema 56 9.713
52
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 9.713
53
INT002 Intermittent Claudication 56 9.713
54
CRB037 Cerebral Palsy 54 9.713
55
P ECL001 Eclampsia 54 9.713
56
PTN001 Patent Foramen Ovale 54 9.713
57
c AFB002 Afibrinogenemia, Congenital 54 9.713
58
c HPT007 Hepatitis E 54 9.713
59
P VNS003 Venous Insufficiency 53 9.713
60
BRG013 Buerger Disease 53 9.713
61
INT075 Intracranial Hypertension 53 9.713
62
c HPT015 Hepatitis D 52 9.713
63
THR016 Thrombophlebitis 52 9.713
64
P END033 Endocarditis 52 9.713
65
VND001 Vein Disease 52 9.713
66
SCT005 Scott Syndrome 50 9.713
67
INF034 Infective Endocarditis 50 9.713
68
PLC005 Placental Insufficiency 50 9.713
69
BRN082 Bernard-Soulier Syndrome, Type C 50 9.713
70
c ACT134 Acute Liver Failure 50 9.713
71
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 9.713
72
PST095 Post-Thrombotic Syndrome 50 9.713
73
HLL004 Hellp Syndrome 49 9.713
74
P CHL066 Cholangitis 49 9.713
75
P CMP008 Compartment Syndrome 48 9.713
76
OBS001 Obstructive Jaundice 48 9.713
77
PPL021 Papilledema 48 9.713
78
PLC007 Placental Abruption 47 9.713
79
BLR008 Bilirubin Metabolic Disorder 47 9.713
80
CVR006 Cavernous Hemangioma 46 9.713
81
OST003 Osteonecrosis 45 9.713
82
ESP002 Esophageal Varix 44 9.713
83
c HMG003 Hemoglobin E Disease 44 9.713
84
SND002 Sneddon Syndrome 44 9.713
85
P RTN014 Retinal Artery Occlusion 43 9.713
86
HPT008 Hepatic Tuberculosis 42 9.713
87
P PRP034 Purpura Fulminans 42 9.713
88
HPT004 Hepatic Coma 40 9.713
89
ISC015 Ischemic Colitis 40 9.713
90
P RTN022 Retinal Vein Occlusion 37 9.713
91
VTM001 Vitamin K Deficiency Hemorrhagic Disease 36 9.713
92
c CNT016 Central Retinal Vein Occlusion 35 9.713
93
CHL039 Choledocholithiasis 34 9.713
94
SGT001 Sagittal Sinus Thrombosis 33 9.713
95
c PRT045 Prothrombin-Related Thrombophilia 23 9.713
96
P MYC007 Myocardial Infarction 79 7.930
97
P RSP003 Respiratory Failure 70 7.930
98
P PRC031 Preeclampsia/eclampsia 1 57 7.930
99
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 7.930
100
ART111 Artery Disease 57 7.930
101
P HMP007 Hemophilia 56 7.930
102
P HMR012 Hemorrhagic Fever 55 7.930
103
HNT002 Hantavirus Pulmonary Syndrome 51 7.930
104
IMM136 Immune System Disease 50 7.930
105
P SCK002 Sick Sinus Syndrome 50 7.930
106
VNW005 Von Willebrand Disease, Type 1 50 7.930
107
STR081 Stormorken Syndrome 50 7.930
108
SPL012 Splenic Disease 47 7.930
109
P PRN026 Porencephaly 47 7.930
110
VLV011 Vulvovaginal Candidiasis 46 7.930
111
ACT058 Active Peptic Ulcer Disease 46 7.930
112
ISC002 Ischemic Optic Neuropathy 46 7.930
113
P AFB001 Afibrinogenemia 46 7.930
114
P ANL018 Analbuminemia 46 7.930
115
c SVR056 Severe Hemophilia a 46 7.930
116
P BLD051 Blood Coagulation Disease 45 7.930
117
KWS001 Kwashiorkor 44 7.930
118
HPT020 Hepatic Vascular Disease 44 7.930
119
CRD001 Cardiac Tamponade 44 7.930
120
HRT008 Heart Conduction Disease 43 7.930
121
c CHR064 Chronic Monocytic Leukemia 43 7.930
122
THR035 Thrombasthenia 42 7.930
123
MRB001 Marburg Hemorrhagic Fever 41 7.930
124
P DYS026 Dysfibrinogenemia 41 7.930
125
PRP028 Peripheral Vertigo 41 7.930
126
SQM002 Squamous Cell Papilloma 41 7.930
127
ENT001 Enterocele 41 7.930
128
BLD054 Blood Protein Disease 40 7.930
129
KRN001 Korean Hemorrhagic Fever 40 7.930
130
c INH004 Inherited Blood Coagulation Disease 39 7.930
131
BRN026 Branch Retinal Artery Occlusion 39 7.930
132
HYP016 Hypochondriasis 39 7.930
133
ISC005 Ischemic Bone Disease 38 7.930
134
FRY001 Frey Syndrome 37 7.930
135
CHR466 Chronic Thromboembolic Pulmonary Hypertension 37 7.930
136
LCH001 Leech Infestation 37 7.930
137
VRT001 Vertebral Artery Occlusion 37 7.930
138
SPN185 Spinal Cord Infarction 36 7.930
139
END013 Endometrial Small Cell Carcinoma 36 7.930
140
SPL006 Splenic Infarction 35 7.930
141
INT010 Intracranial Embolism 35 7.930
142
BSL004 Basilar Artery Occlusion 35 7.930
143
BLT003 Blue Toe Syndrome 35 7.930
144
FMR003 Femoral Neuropathy 34 7.930
145
ABD004 Abdominal Tuberculosis 34 7.930
146
RTN021 Retinal Vascular Occlusion 34 7.930
147
MSN003 Mesenteric Vascular Occlusion 34 7.930
148
FRN014 Fournier Gangrene 34 7.930
149
HMC014 Homocysteinemia 34 7.930
150
ISC001 Ischemic Neuropathy 33 7.930
151
SBN001 Subendocardial Myocardial Infarction 33 7.930
152
VSC008 Vascular Hemostatic Disease 33 7.930
153
GNT005 Giant Hemangioma 33 7.930
154
ORB007 Orbital Cyst 33 7.930
155
QLT001 Qualitative Platelet Defect 32 7.930
156
MRN001 Marantic Endocarditis 32 7.930
157
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 7.930
158
PLS002 Peliosis Hepatis 31 7.930
159
LVD002 Livedoid Vasculopathy 31 7.930
160
INT050 Intestinal Impaction 31 7.930
161
LWR004 Lower Urinary Tract Calculus 31 7.930
162
EXH001 Exhibitionism 30 7.930
163
SDD008 Sudden Sensorineural Hearing Loss 30 7.930
164
ANT013 Anterior Spinal Artery Syndrome 29 7.930
165
EPS001 Epstein-Barr Virus Hepatitis 29 7.930
166
SPR011 Suprasellar Meningioma 29 7.930
167
TYL001 Taylor's Syndrome 29 7.930
168
ASC003 Ascending Cholangitis 29 7.930
169
URT011 Urethral Calculus 28 7.930
170
PRC051 Paracetamol Poisoning 27 7.930
171
MXL016 Maxillonasal Dysplasia, Binder Type 27 7.930
172
PRM008 Parametritis 27 7.930
173
ECC005 Eccrine Adenocarcinoma 27 7.930
174
ANT022 Anterior Cranial Fossa Meningioma 26 7.930
175
c MLG042 Malignant Otitis Externa 26 7.930
176
CNR001 Coenurosis 25 7.930
177
PRL015 Prolapse of Female Genital Organ 22 7.930
178
c ANT010 Anterior Compartment Syndrome 22 7.930
179
PHN001 Phencyclidine Abuse 21 7.930
180
HPT066 Hepatoportal Sclerosis 20 7.930
181
DSS006 Disuse Amblyopia 20 7.930
182
NNH002 Non-a-E Hepatitis 19 7.930
183
CRB017 Cerebral Falx Meningioma 18 7.930
184
HLR004 Hilar Cholangiocellular Carcinoma 15 7.930
185
URT015 Urethral False Passage 11 7.930
186
P GST049 Gastrointestinal System Cancer 60 5.608
187
GST050 Gastrointestinal System Disease 54 5.608
188
BLR006 Biliary Tract Disease 51 5.608
189
BLD036 Bile Duct Disease 48 5.608
190
BLD053 Blood Platelet Disease 46 5.608
191
CRB132 Cerebral Sinovenous Thrombosis 31 5.608