Search results for "F2"

145 hits were found for 'F2'

# Family MCID Name MIFTS Score
1
P INH005 Inherited Hypoprothrombinemia 13 4.374
2
PRT012 Prothrombin Deficiency 43 3.341
3
THR079 Thromboembolism 67 3.093
4
P THR015 Thrombophilia 66 3.093
5
FCT007 Factor Vii Deficiency 80 2.525
6
P HMP004 Hemophilia B 80 2.525
7
LVR012 Liver Cirrhosis 76 2.525
8
ANT006 Antiphospholipid Syndrome 68 2.525
9
P LVR013 Liver Disease 68 2.525
10
FCT006 Factor V Deficiency 66 2.525
11
FCT003 Factor X Deficiency 65 2.525
12
PLM033 Pulmonary Embolism 65 2.525
13
c HMP007 Hemophilia 64 2.525
14
P BRN019 Bernard-Soulier Syndrome 64 2.525
15
FCT002 Factor Xi Deficiency 64 2.525
16
PRT014 Protein S Deficiency 64 2.525
17
c VRL010 Viral Hepatitis 63 2.525
18
c AFB001 Afibrinogenemia 63 2.525
19
DYS026 Dysfibrinogenemia 62 2.525
20
DSS009 Disseminated Intravascular Coagulation 61 2.525
21
VNS009 Venous Thrombosis 59 2.525
22
c HPT003 Hepatitis a 58 2.525
23
ANT009 Antithrombin Iii Deficiency 58 2.525
24
ALC006 Alcoholic Hepatitis 57 2.525
25
HPT014 Hepatorenal Syndrome 56 2.525
26
PRT018 Portal Vein Thrombosis 54 2.525
27
c HPT007 Hepatitis E 52 2.525
28
SCT005 Scott Syndrome 50 2.525
29
PRG060 Pregnancy Loss 47 2.525
30
c THR092 Thrombophilia Due to Thrombin Defect 8 2.525
31
PRT045 Prothrombin-Related Thrombophilia 30 2.215
32
VNS010 Venous Thromboembolism 54 2.187
33
PRG096 Pregnancy Loss, Recurrent 2 7 2.187
34
FCT001 Factor Viii Deficiency 74 1.786
35
c HPT016 Hepatitis B 68 1.786
36
PSD007 Pseudomyxoma Peritonei 68 1.786
37
THR016 Thrombophlebitis 68 1.786
38
CRY005 Cryptococcosis 67 1.786
39
P ABD003 Abdominal Aortic Aneurysm 67 1.786
40
FCT004 Factor Xii Deficiency 66 1.786
41
GST009 Gastroschisis 66 1.786
42
VLV011 Vulvovaginal Candidiasis 66 1.786
43
P PRT013 Portal Hypertension 65 1.786
44
STR067 Stroke, Ischemic 64 1.786
45
c MLG054 Malignant Histiocytosis 62 1.786
46
SND002 Sneddon Syndrome 60 1.786
47
SCB001 Scabies 60 1.786
48
BTL001 Botulism 60 1.786
49
P ANT058 Anterior Ischemic Optic Neuropathy 58 1.786
50
CVR006 Cavernous Hemangioma 58 1.786
51
HYP063 Hypersplenism 58 1.786
52
c SCK002 Sick Sinus Syndrome 57 1.786
53
P CNG019 Congenital Afibrinogenemia 57 1.786
54
c ISC002 Ischemic Optic Neuropathy 57 1.786
55
c CNT016 Central Retinal Vein Occlusion 57 1.786
56
c RTN014 Retinal Artery Occlusion 57 1.786
57
c HPT015 Hepatitis D 56 1.786
58
PSD002 Pseudotumor Cerebri 56 1.786
59
P CMP008 Compartment Syndrome 55 1.786
60
ACT095 Acute Biphenotypic Leukemia 54 1.786
61
PPL021 Papilledema 53 1.786
62
c ACT134 Acute Liver Failure 53 1.786
63
c INT001 Intrahepatic Cholestasis 53 1.786
64
P CNT028 Central Retinal Artery Occlusion 52 1.786
65
HNT002 Hantavirus Pulmonary Syndrome 52 1.786
66
ISC015 Ischemic Colitis 52 1.786
67
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 50 1.786
68
FCT005 Factor Xiii Deficiency 50 1.786
69
ACT099 Acute Fatty Liver of Pregnancy 49 1.786
70
c SVR056 Severe Hemophilia a 49 1.786
71
HYP026 Hypoglycemic Coma 49 1.786
72
NNT016 Neonatal Hemochromatosis 49 1.786
73
MDT001 Mediterranean Spotted Fever 48 1.786
74
HMC014 Homocysteinemia 48 1.786
75
P WRF002 Warfarin Sensitivity 48 1.786
76
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 47 1.786
77
c PRN026 Porencephaly 47 1.786
78
CHL039 Choledocholithiasis 47 1.786
79
ACQ017 Acquired Von Willebrand Syndrome 46 1.786
80
HPT008 Hepatic Tuberculosis 46 1.786
81
ABD004 Abdominal Tuberculosis 46 1.786
82
P HMR005 Hemorrhoid 46 1.786
83
LYM012 Lymphoplasmacytic Lymphoma 46 1.786
84
P HMG003 Hemoglobin E Disease 45 1.786
85
ART110 Arteritic Anterior Ischemic Optic Neuropathy 44 1.786
86
VND001 Vein Disease 44 1.786
87
CRT012 Cortical Blindness 43 1.786
88
HPT004 Hepatic Coma 43 1.786
89
SPN185 Spinal Cord Infarction 42 1.786
90
PST095 Post-Thrombotic Syndrome 42 1.786
91
ESP002 Esophageal Varix 41 1.786
92
WRF001 Warfarin Resistance 41 1.786
93
PRP028 Peripheral Vertigo 40 1.786
94
WND001 Wound Botulism 40 1.786
95
VTM001 Vitamin K Deficiency Hemorrhagic Disease 39 1.786
96
PRS021 Prostatic Adenoma 38 1.786
97
BLD054 Blood Protein Disease 37 1.786
98
HNS001 Hansen's Disease 37 1.786
99
CTR003 Citrin Deficiency 37 1.786
100
MTH044 Mthfr Gene Mutation 32 1.786
101
HPT066 Hepatoportal Sclerosis 32 1.786
102
FLM003 Fulminant Viral Hepatitis 30 1.786
103
ANT013 Anterior Spinal Artery Syndrome 26 1.786
104
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 22 1.786
105
BND003 Binder Syndrome 19 1.786
106
NNH002 Non-a-E Hepatitis 18 1.786
107
CRB132 Cerebral Sinovenous Thrombosis 42 1.263
108
VNS011 Venous Thrombosis, Protection Against 18 1.263
109
OCL010 Ocular Hypotension 28 0.091
110
VGN023 Vaginitis 62 0.074
111
FSC002 Fascioliasis 61 0.074
112
P END046 Endometritis 40 0.074
113
BYS001 Byssinosis 31 0.074
114
P TYP008 Type 1 Diabetes Mellitus 95 0.053
115
P SYS001 Systemic Lupus Erythematosus 89 0.053
116
P OST002 Osteoporosis 76 0.053
117
c LPS004 Lupus Erythematosus 75 0.053
118
P ART022 Arthritis 74 0.053
119
c DBT009 Diabetes Mellitus 73 0.053
120
MSL001 Measles 67 0.053
121
CLT003 Colitis 64 0.053
122
PRT037 Pertussis 61 0.053
123
SCK005 Sickle Cell Disease 61 0.053
124
GNG013 Gingivitis 60 0.053
125
OLG003 Oligohydramnios 59 0.053
126
SLD003 Sialadenitis 59 0.053
127
P GLB002 Glioblastoma 58 0.053
128
P ADN016 Adenocarcinoma 58 0.053
129
ANN002 Anencephaly 58 0.053
130
OST016 Osteochondrosis 58 0.053
131
PRT039 Proteinuria 57 0.053
132
ACT017 Acute Chest Syndrome 56 0.053
133
P ZLL001 Zellweger Syndrome 54 0.053
134
ANG011 Angiodysplasia 54 0.053
135
BLN003 Blindness 52 0.053
136
LYM027 Lymphopenia 50 0.053
137
END041 Endometrial Adenocarcinoma 50 0.053
138
PYL006 Pyloric Stenosis 49 0.053
139
HYP009 Hypertrophic Pyloric Stenosis 49 0.053
140
P CLL015 Collagen Disease 49 0.053
141
ECT026 Ectopic Pregnancy 45 0.053
142
ILS001 Ileus 44 0.053
143
NPH017 Nephrosis 42 0.053
144
PRL008 Paralytic Ileus 36 0.053
145
FML031 Female Stress Incontinence 29 0.053