Search results for "[genes] F2"

101 hits were found for '[genes] F2'

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 54 19.669
2
P THR015 Thrombophilia 57 15.236
3
c HMP004 Hemophilia B 72 12.440
4
FCT007 Factor Vii Deficiency 70 12.440
5
c HMP029 Hemophilia a 66 12.440
6
LVR012 Liver Cirrhosis 66 12.440
7
P LVR013 Liver Disease 62 12.440
8
P HMP007 Hemophilia 59 12.440
9
FCT003 Factor X Deficiency 58 12.440
10
ALC006 Alcoholic Hepatitis 58 12.440
11
FCT006 Factor V Deficiency 58 12.440
12
PLM033 Pulmonary Embolism 56 12.440
13
P ANT006 Antiphospholipid Syndrome 55 12.440
14
PRT014 Protein S Deficiency 55 12.440
15
P AFB001 Afibrinogenemia 55 12.440
16
c VRL010 Viral Hepatitis 54 12.440
17
DSS009 Disseminated Intravascular Coagulation 52 12.440
18
P DYS026 Dysfibrinogenemia 52 12.440
19
c HPT003 Hepatitis a 51 12.440
20
HPT014 Hepatorenal Syndrome 48 12.440
21
PRT018 Portal Vein Thrombosis 47 12.440
22
SCT005 Scott Syndrome 45 12.440
23
c HPT007 Hepatitis E 45 12.440
24
c THR092 Thrombophilia Due to Thrombin Defect 41 12.440
25
PRT012 Prothrombin Deficiency 29 10.773
26
PRT045 Prothrombin-Related Thrombophilia 26 10.773
27
PRG096 Pregnancy Loss, Recurrent 2 9 10.773
28
HPT023 Hepatocellular Carcinoma 95 8.796
29
STR067 Stroke, Ischemic 65 8.796
30
P ATR011 Atrial Fibrillation 62 8.796
31
c HPT016 Hepatitis B 60 8.796
32
PSD007 Pseudomyxoma Peritonei 59 8.796
33
P ABD003 Abdominal Aortic Aneurysm 58 8.796
34
THR016 Thrombophlebitis 58 8.796
35
CRY005 Cryptococcosis 58 8.796
36
FCT004 Factor Xii Deficiency 58 8.796
37
VLV011 Vulvovaginal Candidiasis 56 8.796
38
GST009 Gastroschisis 55 8.796
39
P INT001 Intrahepatic Cholestasis 55 8.796
40
c MLG054 Malignant Histiocytosis 55 8.796
41
SND002 Sneddon Syndrome 54 8.796
42
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 8.796
43
FNC009 Fanconi-Bickel Syndrome 52 8.796
44
BTL001 Botulism 52 8.796
45
FCT001 Factor Viii Deficiency 51 8.796
46
SCB001 Scabies 50 8.796
47
P SCK002 Sick Sinus Syndrome 50 8.796
48
c HPT015 Hepatitis D 50 8.796
49
CVR006 Cavernous Hemangioma 50 8.796
50
HYP063 Hypersplenism 50 8.796
51
ACT095 Acute Biphenotypic Leukemia 49 8.796
52
c CNT016 Central Retinal Vein Occlusion 49 8.796
53
P PRT013 Portal Hypertension 49 8.796
54
ISC002 Ischemic Optic Neuropathy 49 8.796
55
P PRN026 Porencephaly 48 8.796
56
c ACT134 Acute Liver Failure 48 8.796
57
P RTN014 Retinal Artery Occlusion 47 8.796
58
P CMP008 Compartment Syndrome 47 8.796
59
PSD002 Pseudotumor Cerebri 47 8.796
60
CRB153 Cerebral Arteriovenous Malformation 46 8.796
61
PPL021 Papilledema 46 8.796
62
HNT002 Hantavirus Pulmonary Syndrome 46 8.796
63
ISC015 Ischemic Colitis 45 8.796
64
c CNT028 Central Retinal Artery Occlusion 45 8.796
65
FCT005 Factor Xiii Deficiency 44 8.796
66
c SVR056 Severe Hemophilia a 43 8.796
67
LYM012 Lymphoplasmacytic Lymphoma 43 8.796
68
MDT001 Mediterranean Spotted Fever 43 8.796
69
NNT016 Neonatal Hemochromatosis 41 8.796
70
P HMR005 Hemorrhoid 41 8.796
71
HYP026 Hypoglycemic Coma 41 8.796
72
ACQ017 Acquired Von Willebrand Syndrome 41 8.796
73
HMC014 Homocysteinemia 40 8.796
74
ABD004 Abdominal Tuberculosis 39 8.796
75
HPT008 Hepatic Tuberculosis 39 8.796
76
CHL039 Choledocholithiasis 39 8.796
77
c HMG003 Hemoglobin E Disease 39 8.796
78
ART110 Arteritic Anterior Ischemic Optic Neuropathy 38 8.796
79
VND001 Vein Disease 38 8.796
80
CRT012 Cortical Blindness 36 8.796
81
SPN185 Spinal Cord Infarction 36 8.796
82
PST095 Post-Thrombotic Syndrome 36 8.796
83
HPT004 Hepatic Coma 35 8.796
84
ESP002 Esophageal Varix 35 8.796
85
PRP028 Peripheral Vertigo 34 8.796
86
VTM001 Vitamin K Deficiency Hemorrhagic Disease 32 8.796
87
WND001 Wound Botulism 32 8.796
88
PRS021 Prostatic Adenoma 32 8.796
89
HNS001 Hansen's Disease 31 8.796
90
BLD054 Blood Protein Disease 31 8.796
91
HPT066 Hepatoportal Sclerosis 28 8.796
92
FLM003 Fulminant Viral Hepatitis 26 8.796
93
MTH044 Mthfr Gene Mutation 25 8.796
94
BND003 Binder Syndrome 24 8.796
95
HRD160 Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors 21 8.796
96
ANT013 Anterior Spinal Artery Syndrome 21 8.796
97
c INH005 Inherited Hypoprothrombinemia 21 8.796
98
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 19 8.796
99
NNH002 Non-a-E Hepatitis 15 8.796
100
P PLM037 Pulmonary Hypertension 85 6.220
101
CRB132 Cerebral Sinovenous Thrombosis 37 6.220