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