Search results for "F2"

141 hits were found for 'F2'

# Family MCID Name MIFTS Score
1
P INH005 Inherited Hypoprothrombinemia 13 4.205
2
PRT012 Prothrombin Deficiency 38 3.106
3
FCT007 Factor Vii Deficiency 78 2.536
4
P HMP004 Hemophilia B 77 2.536
5
LVR012 Liver Cirrhosis 75 2.536
6
P LVR013 Liver Disease 69 2.536
7
PRT014 Protein S Deficiency 67 2.536
8
c HMP007 Hemophilia 67 2.536
9
ANT006 Antiphospholipid Syndrome 65 2.536
10
P BRN019 Bernard-Soulier Syndrome 64 2.536
11
FCT002 Factor Xi Deficiency 64 2.536
12
THR079 Thromboembolism 64 2.536
13
PLM033 Pulmonary Embolism 64 2.536
14
c VRL010 Viral Hepatitis 64 2.536
15
FCT003 Factor X Deficiency 63 2.536
16
FCT006 Factor V Deficiency 63 2.536
17
DSS009 Disseminated Intravascular Coagulation 62 2.536
18
ANT009 Antithrombin Iii Deficiency 60 2.536
19
c AFB001 Afibrinogenemia 60 2.536
20
c HPT003 Hepatitis a 59 2.536
21
ALC006 Alcoholic Hepatitis 57 2.536
22
HPT014 Hepatorenal Syndrome 56 2.536
23
VNS009 Venous Thrombosis 55 2.536
24
PRT018 Portal Vein Thrombosis 54 2.536
25
P DYS026 Dysfibrinogenemia 52 2.536
26
c HPT007 Hepatitis E 52 2.536
27
SCT005 Scott Syndrome 50 2.536
28
PRG060 Pregnancy Loss 47 2.536
29
PRT045 Prothrombin-Related Thrombophilia 28 2.224
30
c THR092 Thrombophilia Due to Thrombin Defect 8 2.196
31
HPT023 Hepatocellular Carcinoma 79 1.793
32
FCT001 Factor Viii Deficiency 70 1.793
33
THR016 Thrombophlebitis 68 1.793
34
CRY005 Cryptococcosis 68 1.793
35
c HPT016 Hepatitis B 68 1.793
36
PSD007 Pseudomyxoma Peritonei 67 1.793
37
P ABD003 Abdominal Aortic Aneurysm 67 1.793
38
GST009 Gastroschisis 66 1.793
39
VLV011 Vulvovaginal Candidiasis 66 1.793
40
P PRT013 Portal Hypertension 66 1.793
41
FCT004 Factor Xii Deficiency 65 1.793
42
STR067 Stroke, Ischemic 64 1.793
43
c MLG054 Malignant Histiocytosis 63 1.793
44
BTL001 Botulism 60 1.793
45
SND002 Sneddon Syndrome 59 1.793
46
ANT058 Anterior Ischemic Optic Neuropathy 59 1.793
47
SCB001 Scabies 59 1.793
48
CVR006 Cavernous Hemangioma 58 1.793
49
HYP063 Hypersplenism 58 1.793
50
P CNG019 Congenital Afibrinogenemia 58 1.793
51
c HPT015 Hepatitis D 57 1.793
52
c RTN014 Retinal Artery Occlusion 57 1.793
53
ACT095 Acute Biphenotypic Leukemia 56 1.793
54
c SCK002 Sick Sinus Syndrome 56 1.793
55
PPL021 Papilledema 56 1.793
56
P CMP008 Compartment Syndrome 56 1.793
57
c CNT016 Central Retinal Vein Occlusion 55 1.793
58
PSD002 Pseudotumor Cerebri 55 1.793
59
c ACT134 Acute Liver Failure 53 1.793
60
HNT002 Hantavirus Pulmonary Syndrome 53 1.793
61
VNS010 Venous Thromboembolism 53 1.793
62
c INT001 Intrahepatic Cholestasis 52 1.793
63
P CNT028 Central Retinal Artery Occlusion 52 1.793
64
PRP034 Purpura Fulminans 52 1.793
65
HYP026 Hypoglycemic Coma 49 1.793
66
FCT005 Factor Xiii Deficiency 49 1.793
67
ACT099 Acute Fatty Liver of Pregnancy 49 1.793
68
c SVR056 Severe Hemophilia a 49 1.793
69
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 48 1.793
70
HMC014 Homocysteinemia 48 1.793
71
MDT001 Mediterranean Spotted Fever 48 1.793
72
NNT016 Neonatal Hemochromatosis 47 1.793
73
c PRN026 Porencephaly 47 1.793
74
CHL039 Choledocholithiasis 47 1.793
75
ACQ017 Acquired Von Willebrand Syndrome 47 1.793
76
ABD004 Abdominal Tuberculosis 46 1.793
77
HPT008 Hepatic Tuberculosis 46 1.793
78
P WRF002 Warfarin Sensitivity 46 1.793
79
P HMR005 Hemorrhoid 46 1.793
80
P HMG003 Hemoglobin E Disease 45 1.793
81
LYM012 Lymphoplasmacytic Lymphoma 44 1.793
82
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 44 1.793
83
VND001 Vein Disease 44 1.793
84
ART110 Arteritic Anterior Ischemic Optic Neuropathy 43 1.793
85
HPT004 Hepatic Coma 43 1.793
86
SPN185 Spinal Cord Infarction 42 1.793
87
ESP002 Esophageal Varix 42 1.793
88
PRP028 Peripheral Vertigo 40 1.793
89
WND001 Wound Botulism 39 1.793
90
WRF001 Warfarin Resistance 39 1.793
91
PST095 Post-Thrombotic Syndrome 39 1.793
92
PRS021 Prostatic Adenoma 38 1.793
93
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 1.793
94
CTR003 Citrin Deficiency 37 1.793
95
BLD054 Blood Protein Disease 36 1.793
96
HNS001 Hansen's Disease 36 1.793
97
CRT012 Cortical Blindness 34 1.793
98
MTH044 Mthfr Gene Mutation 32 1.793
99
HPT066 Hepatoportal Sclerosis 32 1.793
100
FLM003 Fulminant Viral Hepatitis 30 1.793
101
ANT013 Anterior Spinal Artery Syndrome 25 1.793
102
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 22 1.793
103
BND003 Binder Syndrome 19 1.793
104
NNH002 Non-a-E Hepatitis 17 1.793
105
PRG096 Pregnancy Loss, Recurrent 2 6 1.793
106
CRB132 Cerebral Sinovenous Thrombosis 42 1.268
107
OCL010 Ocular Hypotension 29 0.092
108
FSC002 Fascioliasis 62 0.075
109
VGN023 Vaginitis 62 0.075
110
P END046 Endometritis 40 0.075
111
BYS001 Byssinosis 30 0.075
112
P TYP008 Type 1 Diabetes Mellitus 93 0.053
113
P SYS001 Systemic Lupus Erythematosus 85 0.053
114
c DBT009 Diabetes Mellitus 78 0.053
115
P ART022 Arthritis 75 0.053
116
P OST002 Osteoporosis 75 0.053
117
c LPS004 Lupus Erythematosus 72 0.053
118
MSL001 Measles 67 0.053
119
GNG013 Gingivitis 62 0.053
120
PRT037 Pertussis 61 0.053
121
OLG003 Oligohydramnios 59 0.053
122
SLD003 Sialadenitis 59 0.053
123
SCK005 Sickle Cell Disease 58 0.053
124
OST016 Osteochondrosis 58 0.053
125
ANN002 Anencephaly 58 0.053
126
P ADN016 Adenocarcinoma 58 0.053
127
PRT039 Proteinuria 57 0.053
128
ACT017 Acute Chest Syndrome 56 0.053
129
ANG011 Angiodysplasia 54 0.053
130
BLN003 Blindness 52 0.053
131
P ZLL001 Zellweger Syndrome 52 0.053
132
LYM027 Lymphopenia 51 0.053
133
PYL006 Pyloric Stenosis 50 0.053
134
END041 Endometrial Adenocarcinoma 49 0.053
135
HYP009 Hypertrophic Pyloric Stenosis 49 0.053
136
P CLL015 Collagen Disease 49 0.053
137
ECT026 Ectopic Pregnancy 45 0.053
138
ILS001 Ileus 44 0.053
139
NPH017 Nephrosis 42 0.053
140
PRL008 Paralytic Ileus 36 0.053
141
FML031 Female Stress Incontinence 29 0.053