Search results for "F2"

143 hits were found for 'F2'

# Family MCID Name MIFTS Score
1
P HYP620 Hypoprothrombinemia 54 4.084
2
P THR015 Thrombophilia 57 3.156
3
c THR092 Thrombophilia Due to Thrombin Defect 41 2.631
4
ALC006 Alcoholic Hepatitis 58 2.569
5
c HMP004 Hemophilia B 72 2.545
6
FCT007 Factor Vii Deficiency 70 2.545
7
LVR012 Liver Cirrhosis 66 2.545
8
c HMP029 Hemophilia a 66 2.545
9
P LVR013 Liver Disease 62 2.545
10
P HMP007 Hemophilia 59 2.545
11
FCT003 Factor X Deficiency 58 2.545
12
FCT006 Factor V Deficiency 58 2.545
13
PLM033 Pulmonary Embolism 56 2.545
14
P ANT006 Antiphospholipid Syndrome 55 2.545
15
PRT014 Protein S Deficiency 55 2.545
16
P AFB001 Afibrinogenemia 55 2.545
17
c VRL010 Viral Hepatitis 54 2.545
18
DSS009 Disseminated Intravascular Coagulation 52 2.545
19
P DYS026 Dysfibrinogenemia 52 2.545
20
c HPT003 Hepatitis a 51 2.545
21
HPT014 Hepatorenal Syndrome 48 2.545
22
PRT018 Portal Vein Thrombosis 47 2.545
23
SCT005 Scott Syndrome 45 2.545
24
c HPT007 Hepatitis E 45 2.545
25
PRG096 Pregnancy Loss, Recurrent 2 9 2.256
26
PRT045 Prothrombin-Related Thrombophilia 26 2.232
27
PRT012 Prothrombin Deficiency 29 2.204
28
c INH005 Inherited Hypoprothrombinemia 21 1.907
29
HPT023 Hepatocellular Carcinoma 95 1.799
30
STR067 Stroke, Ischemic 65 1.799
31
P ATR011 Atrial Fibrillation 62 1.799
32
c HPT016 Hepatitis B 60 1.799
33
PSD007 Pseudomyxoma Peritonei 59 1.799
34
P ABD003 Abdominal Aortic Aneurysm 58 1.799
35
THR016 Thrombophlebitis 58 1.799
36
CRY005 Cryptococcosis 58 1.799
37
FCT004 Factor Xii Deficiency 58 1.799
38
VLV011 Vulvovaginal Candidiasis 56 1.799
39
GST009 Gastroschisis 55 1.799
40
P INT001 Intrahepatic Cholestasis 55 1.799
41
c MLG054 Malignant Histiocytosis 55 1.799
42
SND002 Sneddon Syndrome 54 1.799
43
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 1.799
44
BTL001 Botulism 52 1.799
45
FNC009 Fanconi-Bickel Syndrome 52 1.799
46
FCT001 Factor Viii Deficiency 51 1.799
47
SCB001 Scabies 50 1.799
48
P SCK002 Sick Sinus Syndrome 50 1.799
49
c HPT015 Hepatitis D 50 1.799
50
CVR006 Cavernous Hemangioma 50 1.799
51
HYP063 Hypersplenism 50 1.799
52
ACT095 Acute Biphenotypic Leukemia 49 1.799
53
c CNT016 Central Retinal Vein Occlusion 49 1.799
54
P PRT013 Portal Hypertension 49 1.799
55
ISC002 Ischemic Optic Neuropathy 49 1.799
56
P PRN026 Porencephaly 48 1.799
57
c ACT134 Acute Liver Failure 48 1.799
58
P RTN014 Retinal Artery Occlusion 47 1.799
59
P CMP008 Compartment Syndrome 47 1.799
60
PSD002 Pseudotumor Cerebri 47 1.799
61
PPL021 Papilledema 46 1.799
62
HNT002 Hantavirus Pulmonary Syndrome 46 1.799
63
CRB153 Cerebral Arteriovenous Malformation 46 1.799
64
ISC015 Ischemic Colitis 45 1.799
65
c CNT028 Central Retinal Artery Occlusion 45 1.799
66
FCT005 Factor Xiii Deficiency 44 1.799
67
c SVR056 Severe Hemophilia a 43 1.799
68
LYM012 Lymphoplasmacytic Lymphoma 43 1.799
69
MDT001 Mediterranean Spotted Fever 43 1.799
70
NNT016 Neonatal Hemochromatosis 41 1.799
71
P HMR005 Hemorrhoid 41 1.799
72
HYP026 Hypoglycemic Coma 41 1.799
73
ACQ017 Acquired Von Willebrand Syndrome 41 1.799
74
HMC014 Homocysteinemia 40 1.799
75
ABD004 Abdominal Tuberculosis 39 1.799
76
HPT008 Hepatic Tuberculosis 39 1.799
77
CHL039 Choledocholithiasis 39 1.799
78
c HMG003 Hemoglobin E Disease 39 1.799
79
ART110 Arteritic Anterior Ischemic Optic Neuropathy 38 1.799
80
VND001 Vein Disease 38 1.799
81
CRT012 Cortical Blindness 36 1.799
82
SPN185 Spinal Cord Infarction 36 1.799
83
PST095 Post-Thrombotic Syndrome 36 1.799
84
ESP002 Esophageal Varix 35 1.799
85
HPT004 Hepatic Coma 35 1.799
86
PRP028 Peripheral Vertigo 34 1.799
87
VTM001 Vitamin K Deficiency Hemorrhagic Disease 32 1.799
88
WND001 Wound Botulism 32 1.799
89
PRS021 Prostatic Adenoma 32 1.799
90
HNS001 Hansen's Disease 31 1.799
91
BLD054 Blood Protein Disease 31 1.799
92
HPT066 Hepatoportal Sclerosis 28 1.799
93
FLM003 Fulminant Viral Hepatitis 26 1.799
94
MTH044 Mthfr Gene Mutation 25 1.799
95
BND003 Binder Syndrome 24 1.799
96
ANT013 Anterior Spinal Artery Syndrome 21 1.799
97
HRD160 Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors 21 1.799
98
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 19 1.799
99
NNH002 Non-a-E Hepatitis 15 1.799
100
P PLM037 Pulmonary Hypertension 85 1.272
101
CRB132 Cerebral Sinovenous Thrombosis 37 1.272
102
OCL010 Ocular Hypotension 23 0.090
103
FSC002 Fascioliasis 53 0.074
104
VGN023 Vaginitis 51 0.074
105
P END046 Endometritis 34 0.074
106
BYS001 Byssinosis 26 0.074
107
c SYS001 Systemic Lupus Erythematosus 91 0.052
108
P BRS047 Breast Cancer 90 0.052
109
P OST002 Osteoporosis 71 0.052
110
BHC002 Behcet's Disease 68 0.052
111
P LPS004 Lupus Erythematosus 67 0.052
112
P ART022 Arthritis 65 0.052
113
P GLB002 Glioblastoma 59 0.052
114
MSL001 Measles 58 0.052
115
INS024 Insulin-Like Growth Factor I 58 0.052
116
ANN002 Anencephaly 57 0.052
117
CLT003 Colitis 54 0.052
118
PRT037 Pertussis 54 0.052
119
SCK005 Sickle Cell Disease 54 0.052
120
GNG013 Gingivitis 52 0.052
121
OLG003 Oligohydramnios 51 0.052
122
SLD003 Sialadenitis 50 0.052
123
OST016 Osteochondrosis 49 0.052
124
P ADN016 Adenocarcinoma 49 0.052
125
ACT017 Acute Chest Syndrome 48 0.052
126
ANG011 Angiodysplasia 48 0.052
127
P BLN003 Blindness 47 0.052
128
P ZLL001 Zellweger Syndrome 46 0.052
129
PRT039 Proteinuria 43 0.052
130
P CLL015 Collagen Disease 43 0.052
131
LYM027 Lymphopenia 43 0.052
132
END041 Endometrial Adenocarcinoma 43 0.052
133
P HYP009 Hypertrophic Pyloric Stenosis 43 0.052
134
CRV047 Cervical Cancer, Somatic 51 0.052
135
PYL006 Pyloric Stenosis 41 0.052
136
ECT026 Ectopic Pregnancy 39 0.052
137
TNG009 Tongue Squamous Cell Carcinoma 47 0.052
138
ILS001 Ileus 38 0.052
139
NPH017 Nephrosis 36 0.052
140
PRL008 Paralytic Ileus 30 0.052
141
FML031 Female Stress Incontinence 24 0.052
142
c LNG064 Lung Cancer Susceptibility 3 32 0.052
143
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 16 0.052