Search results for "[genes] F2"

201 hits were found for '[genes] F2'

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 54 19.304
2
P LVR013 Liver Disease 75 14.743
3
STR067 Stroke, Ischemic 75 13.650
4
P HPT021 Hepatitis 69 13.650
5
LVR012 Liver Cirrhosis 67 13.650
6
c HPT016 Hepatitis B 65 13.650
7
ALC006 Alcoholic Hepatitis 59 13.650
8
c THR092 Thrombophilia Due to Thrombin Defect 54 13.650
9
P HPT023 Hepatocellular Carcinoma 92 12.460
10
P ATR011 Atrial Fibrillation 66 12.460
11
P THR014 Thrombocytopenia 64 12.460
12
c HMP029 Hemophilia a 63 12.460
13
c HMP004 Hemophilia B 62 12.460
14
FCT003 Factor X Deficiency 61 12.460
15
VNW001 Von Willebrand's Disease 61 12.460
16
FCT007 Factor Vii Deficiency 61 12.460
17
P PRT013 Portal Hypertension 60 12.460
18
PLM033 Pulmonary Embolism 60 12.460
19
c VRL010 Viral Hepatitis 60 12.460
20
c ATM011 Autoimmune Hepatitis 60 12.460
21
P THR015 Thrombophilia 59 12.460
22
THR024 Thrombosis 57 12.460
23
P HMR003 Hemorrhagic Disease 57 12.460
24
P ANT006 Antiphospholipid Syndrome 56 12.460
25
HPT019 Hepatic Encephalopathy 56 12.460
26
THR004 Thrombocytosis 55 12.460
27
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 12.460
28
PRT014 Protein S Deficiency 53 12.460
29
PRT011 Protein C Deficiency 52 12.460
30
P PRM006 Primary Biliary Cirrhosis 51 12.460
31
DSS009 Disseminated Intravascular Coagulation 51 12.460
32
c ACT134 Acute Liver Failure 50 12.460
33
ALC009 Alcoholic Liver Cirrhosis 49 12.460
34
PRT018 Portal Vein Thrombosis 49 12.460
35
HYP063 Hypersplenism 48 12.460
36
HPT014 Hepatorenal Syndrome 46 12.460
37
PRG096 Pregnancy Loss, Recurrent 2 21 12.460
38
SCK003 Sickle Cell Anemia 71 11.145
39
PRP027 Peripheral Vascular Disease 69 11.145
40
CRB037 Cerebral Palsy 66 11.145
41
DNG002 Dengue Hemorrhagic Fever 63 11.145
42
GLN010 Glanzmann Thrombasthenia 63 11.145
43
PRT036 Peritonitis 63 11.145
44
LPT001 Leptospirosis 62 11.145
45
P ADL010 Adult Respiratory Distress Syndrome 61 11.145
46
c HPT003 Hepatitis a 59 11.145
47
CHL068 Cholestasis 59 11.145
48
PRP030 Purpura 58 11.145
49
SCH014 Schistosomiasis 58 11.145
50
FCT006 Factor V Deficiency 57 11.145
51
CHL067 Cholecystitis 57 11.145
52
INT002 Intermittent Claudication 56 11.145
53
P BDD001 Budd-Chiari Syndrome 56 11.145
54
PTN001 Patent Foramen Ovale 55 11.145
55
PLM010 Pulmonary Edema 54 11.145
56
c HPT007 Hepatitis E 54 11.145
57
P END033 Endocarditis 54 11.145
58
c AFB002 Afibrinogenemia, Congenital 54 11.145
59
P ECL001 Eclampsia 54 11.145
60
P VNS003 Venous Insufficiency 54 11.145
61
SCT005 Scott Syndrome 53 11.145
62
BRG013 Buerger Disease 53 11.145
63
SPT005 Spotted Fever 53 11.145
64
THR016 Thrombophlebitis 53 11.145
65
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 11.145
66
c HPT015 Hepatitis D 52 11.145
67
INF034 Infective Endocarditis 51 11.145
68
INT075 Intracranial Hypertension 50 11.145
69
BRN082 Bernard-Soulier Syndrome, Type C 50 11.145
70
PLC005 Placental Insufficiency 50 11.145
71
HLL004 Hellp Syndrome 50 11.145
72
P SCK002 Sick Sinus Syndrome 50 11.145
73
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 11.145
74
OBS001 Obstructive Jaundice 48 11.145
75
P CMP008 Compartment Syndrome 48 11.145
76
VND001 Vein Disease 47 11.145
77
PPL021 Papilledema 47 11.145
78
PLC007 Placental Abruption 47 11.145
79
PST095 Post-Thrombotic Syndrome 47 11.145
80
CVR006 Cavernous Hemangioma 46 11.145
81
OST003 Osteonecrosis 45 11.145
82
SND002 Sneddon Syndrome 44 11.145
83
c HMG003 Hemoglobin E Disease 44 11.145
84
P RTN014 Retinal Artery Occlusion 44 11.145
85
HPT008 Hepatic Tuberculosis 42 11.145
86
BLR008 Bilirubin Metabolic Disorder 42 11.145
87
P CHL066 Cholangitis 42 11.145
88
ESP002 Esophageal Varix 41 11.145
89
P PRP034 Purpura Fulminans 41 11.145
90
ISC015 Ischemic Colitis 39 11.145
91
HPT004 Hepatic Coma 39 11.145
92
P RTN022 Retinal Vein Occlusion 38 11.145
93
c CNT016 Central Retinal Vein Occlusion 36 11.145
94
SGT001 Sagittal Sinus Thrombosis 35 11.145
95
CHL039 Choledocholithiasis 34 11.145
96
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 11.145
97
c PRT045 Prothrombin-Related Thrombophilia 24 11.145
98
P OBS005 Obesity 92 9.652
99
P PLM037 Pulmonary Hypertension 79 9.652
100
P MYC007 Myocardial Infarction 79 9.652
101
P RSP003 Respiratory Failure 71 9.652
102
CRB039 Cerebrovascular Disease 63 9.652
103
P HMP007 Hemophilia 57 9.652
104
P HMR012 Hemorrhagic Fever 56 9.652
105
ART111 Artery Disease 55 9.652
106
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 9.652
107
HNT002 Hantavirus Pulmonary Syndrome 51 9.652
108
IMM136 Immune System Disease 51 9.652
109
STR081 Stormorken Syndrome 49 9.652
110
VNW005 Von Willebrand Disease, Type 1 49 9.652
111
P AFB001 Afibrinogenemia 48 9.652
112
VLV011 Vulvovaginal Candidiasis 48 9.652
113
P PRN026 Porencephaly 48 9.652
114
SPL012 Splenic Disease 46 9.652
115
P DYS026 Dysfibrinogenemia 45 9.652
116
P ANL018 Analbuminemia 44 9.652
117
CRD001 Cardiac Tamponade 44 9.652
118
c SVR056 Severe Hemophilia a 43 9.652
119
ACT058 Active Peptic Ulcer Disease 43 9.652
120
HRT008 Heart Conduction Disease 42 9.652
121
HPT020 Hepatic Vascular Disease 42 9.652
122
P BLD051 Blood Coagulation Disease 42 9.652
123
c CHR064 Chronic Monocytic Leukemia 42 9.652
124
MRB001 Marburg Hemorrhagic Fever 41 9.652
125
KWS001 Kwashiorkor 40 9.652
126
ENT001 Enterocele 40 9.652
127
SQM002 Squamous Cell Papilloma 40 9.652
128
LCH001 Leech Infestation 40 9.652
129
KRN001 Korean Hemorrhagic Fever 39 9.652
130
CHR466 Chronic Thromboembolic Pulmonary Hypertension 39 9.652
131
THR035 Thrombasthenia 39 9.652
132
BRN026 Branch Retinal Artery Occlusion 38 9.652
133
HYP016 Hypochondriasis 38 9.652
134
FMR003 Femoral Neuropathy 38 9.652
135
PRP028 Peripheral Vertigo 38 9.652
136
BLD054 Blood Protein Disease 37 9.652
137
BSL004 Basilar Artery Occlusion 36 9.652
138
c INH004 Inherited Blood Coagulation Disease 36 9.652
139
ISC005 Ischemic Bone Disease 36 9.652
140
BLT003 Blue Toe Syndrome 35 9.652
141
GNT005 Giant Hemangioma 35 9.652
142
FRN014 Fournier Gangrene 35 9.652
143
HMC014 Homocysteinemia 35 9.652
144
SPL006 Splenic Infarction 35 9.652
145
FRY001 Frey Syndrome 35 9.652
146
END013 Endometrial Small Cell Carcinoma 34 9.652
147
MSN003 Mesenteric Vascular Occlusion 34 9.652
148
SPN185 Spinal Cord Infarction 34 9.652
149
ANT013 Anterior Spinal Artery Syndrome 33 9.652
150
ABD004 Abdominal Tuberculosis 32 9.652
151
RTN021 Retinal Vascular Occlusion 32 9.652
152
LVD002 Livedoid Vasculopathy 32 9.652
153
MRN001 Marantic Endocarditis 32 9.652
154
ORB007 Orbital Cyst 32 9.652
155
SBN001 Subendocardial Myocardial Infarction 32 9.652
156
INT010 Intracranial Embolism 32 9.652
157
QLT001 Qualitative Platelet Defect 32 9.652
158
PLS002 Peliosis Hepatis 31 9.652
159
INT050 Intestinal Impaction 31 9.652
160
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 9.652
161
SDD008 Sudden Sensorineural Hearing Loss 31 9.652
162
URT011 Urethral Calculus 31 9.652
163
CRB132 Cerebral Sinovenous Thrombosis 31 9.652
164
VSC008 Vascular Hemostatic Disease 30 9.652
165
ASC003 Ascending Cholangitis 30 9.652
166
ISC001 Ischemic Neuropathy 30 9.652
167
EXH001 Exhibitionism 29 9.652
168
EPS001 Epstein-Barr Virus Hepatitis 29 9.652
169
MXL016 Maxillonasal Dysplasia, Binder Type 28 9.652
170
SPR011 Suprasellar Meningioma 28 9.652
171
ANT022 Anterior Cranial Fossa Meningioma 28 9.652
172
PRM008 Parametritis 27 9.652
173
PRC051 Paracetamol Poisoning 27 9.652
174
ECC005 Eccrine Adenocarcinoma 27 9.652
175
c MLG042 Malignant Otitis Externa 26 9.652
176
TYL001 Taylor's Syndrome 26 9.652
177
CNR001 Coenurosis 25 9.652
178
c ANT010 Anterior Compartment Syndrome 25 9.652
179
PHN001 Phencyclidine Abuse 22 9.652
180
NNH002 Non-a-E Hepatitis 21 9.652
181
CRB017 Cerebral Falx Meningioma 21 9.652
182
PRL015 Prolapse of Female Genital Organ 21 9.652
183
HPT066 Hepatoportal Sclerosis 20 9.652
184
HLR004 Hilar Cholangiocellular Carcinoma 14 9.652
185
URT015 Urethral False Passage 11 9.652
186
P ESS003 Essential Thrombocythemia 70 7.881
187
P GST049 Gastrointestinal System Cancer 60 7.881
188
GST050 Gastrointestinal System Disease 56 7.881
189
BLR006 Biliary Tract Disease 52 7.881
190
BLD036 Bile Duct Disease 48 7.881
191
BLD053 Blood Platelet Disease 46 7.881
192
P ATR010 Atrial Heart Septal Defect 45 7.881
193
VRT001 Vertebral Artery Occlusion 36 7.881
194
HPT081 Hepatic Infarction 34 7.881
195
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 33 7.881
196
ALC001 Alcohol-Related Birth Defect 31 7.881
197
HMN004 Hemangioma of Liver 29 7.881
198
LWR004 Lower Urinary Tract Calculus 28 7.881
199
END074 Endocardium Disease 26 7.881
200
DSS006 Disuse Amblyopia 26 7.881
201
P RTN102 Retinitis Pigmentosa, Y-Linked 23 7.881