Search results for f3

150 hits were found for f3

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 76 2.758
2
c SYS001 Systemic Lupus Erythematosus 86 2.428
3
STR067 Stroke, Ischemic 84 2.428
4
PRP027 Peripheral Vascular Disease 71 2.428
5
c HMP004 Hemophilia B 67 2.428
6
GLN010 Glanzmann Thrombasthenia 66 2.428
7
FCT002 Factor Xi Deficiency 64 2.428
8
c ACT075 Acute Myocardial Infarction 64 2.428
9
ACT119 Acute Promyelocytic Leukemia 64 2.428
10
P THR005 Thrombotic Thrombocytopenic Purpura 63 2.428
11
PLM033 Pulmonary Embolism 62 2.428
12
FCT007 Factor Vii Deficiency 62 2.428
13
VNW001 Von Willebrand's Disease 61 2.428
14
P HMR003 Hemorrhagic Disease 61 2.428
15
P ANT006 Antiphospholipid Syndrome 59 2.428
16
P MNC007 Monocytic Leukemia 59 2.428
17
P THR015 Thrombophilia 58 2.428
18
FCT003 Factor X Deficiency 58 2.428
19
DSS009 Disseminated Intravascular Coagulation 56 2.428
20
THR004 Thrombocytosis 55 2.428
21
FCT004 Factor Xii Deficiency 50 2.428
22
PRT014 Protein S Deficiency 47 2.428
23
CRT004 Carotid Artery Thrombosis 37 2.428
24
c HPT003 Hepatitis a 63 2.131
25
THR024 Thrombosis 61 2.131
26
c THR092 Thrombophilia Due to Thrombin Defect 61 2.131
27
MLR004 Malaria 86 2.103
28
P MYC007 Myocardial Infarction 81 2.103
29
P HRT032 Heart Disease 80 2.103
30
P PLM037 Pulmonary Hypertension 79 2.103
31
VSC007 Vascular Disease 71 2.103
32
c HMP029 Hemophilia a 69 2.103
33
DNG002 Dengue Hemorrhagic Fever 66 2.103
34
c PRC016 Pre-Eclampsia 65 2.103
35
P THR014 Thrombocytopenia 65 2.103
36
SCR008 Scrub Typhus 65 2.103
37
PRP030 Purpura 61 2.103
38
c AFB002 Afibrinogenemia, Congenital 61 2.103
39
PLC005 Placental Insufficiency 59 2.103
40
CRM001 Crimean-Congo Hemorrhagic Fever 58 2.103
41
BDD001 Budd-Chiari Syndrome 58 2.103
42
HNT002 Hantavirus Pulmonary Syndrome 57 2.103
43
HPT046 Hepatic Veno-Occlusive Disease 56 2.103
44
INT075 Intracranial Hypertension 53 2.103
45
HLL004 Hellp Syndrome 53 2.103
46
FCT006 Factor V Deficiency 52 2.103
47
PLC008 Placenta Disease 48 2.103
48
CRN017 Coronary Thrombosis 48 2.103
49
c THR082 Thrombophilia Due to Activated Protein C Resistance 47 2.103
50
FCT005 Factor Xiii Deficiency 46 2.103
51
BLD053 Blood Platelet Disease 45 2.103
52
P PRP034 Purpura Fulminans 44 2.103
53
INT078 Intracranial Thrombosis 37 2.103
54
SGT001 Sagittal Sinus Thrombosis 34 2.103
55
P RSP003 Respiratory Failure 71 1.717
56
P ESS003 Essential Thrombocythemia 71 1.717
57
P ART021 Arteriosclerosis 62 1.717
58
P HMP007 Hemophilia 61 1.717
59
P HMR012 Hemorrhagic Fever 60 1.717
60
IMM136 Immune System Disease 57 1.717
61
INT007 Intermediate Coronary Syndrome 55 1.717
62
ANG054 Angina Pectoris 53 1.717
63
NDL013 Nodular Regenerative Hyperplasia 53 1.717
64
PYD002 Pyoderma 51 1.717
65
c ACQ014 Acquired Hemophilia 51 1.717
66
CFF003 Caffey Disease 51 1.717
67
MLT113 Multicentric Castleman Disease 49 1.717
68
P AFB001 Afibrinogenemia 49 1.717
69
HPR003 Heparin-Induced Thrombocytopenia 48 1.717
70
VND001 Vein Disease 48 1.717
71
LMR001 Lemierre's Syndrome 47 1.717
72
VNW005 Von Willebrand Disease, Type 1 47 1.717
73
PRT012 Prothrombin Deficiency 46 1.717
74
c SVR056 Severe Hemophilia a 46 1.717
75
THR035 Thrombasthenia 46 1.717
76
CTS005 Catastrophic Antiphospholipid Syndrome 45 1.717
77
P ANL018 Analbuminemia 45 1.717
78
c ACQ042 Acquired Hemophilia a 44 1.717
79
LCH001 Leech Infestation 43 1.717
80
SPL012 Splenic Disease 42 1.717
81
KRN001 Korean Hemorrhagic Fever 42 1.717
82
BLD009 Bladder Neck Obstruction 40 1.717
83
SHW001 Shwartzman Phenomenon 40 1.717
84
FMR003 Femoral Neuropathy 39 1.717
85
SQM002 Squamous Cell Papilloma 39 1.717
86
c RTN177 Retinitis Pigmentosa 73 39 1.717
87
FRN014 Fournier Gangrene 38 1.717
88
INT010 Intracranial Embolism 38 1.717
89
P BLD051 Blood Coagulation Disease 38 1.717
90
BLT003 Blue Toe Syndrome 38 1.717
91
CHL010 Childhood Kidney Cell Carcinoma 37 1.717
92
PRP028 Peripheral Vertigo 37 1.717
93
MRN001 Marantic Endocarditis 37 1.717
94
HPT020 Hepatic Vascular Disease 36 1.717
95
PLM013 Pulmonary Immaturity 36 1.717
96
BRN026 Branch Retinal Artery Occlusion 35 1.717
97
DYS013 Dysbaric Osteonecrosis 35 1.717
98
GNT005 Giant Hemangioma 33 1.717
99
c ACT072 Acute Laryngitis 33 1.717
100
QLT001 Qualitative Platelet Defect 32 1.717
101
CRB132 Cerebral Sinovenous Thrombosis 32 1.717
102
ANT022 Anterior Cranial Fossa Meningioma 32 1.717
103
ALC001 Alcohol-Related Birth Defect 32 1.717
104
URT016 Urethral Diverticulum 31 1.717
105
VRT001 Vertebral Artery Occlusion 31 1.717
106
CNJ001 Conjugate Gaze Palsy 30 1.717
107
HPT081 Hepatic Infarction 30 1.717
108
c INH004 Inherited Blood Coagulation Disease 29 1.717
109
INT050 Intestinal Impaction 27 1.717
110
CNG016 Congenital Intrinsic Factor Deficiency 27 1.717
111
INT076 Intracranial Sinus Thrombosis 25 1.717
112
CRB017 Cerebral Falx Meningioma 25 1.717
113
HMM001 Hemometra 23 1.717
114
MXD019 Mixed Malaria 23 1.717
115
END074 Endocardium Disease 22 1.717
116
BLV001 Bolivian Hemorrhagic Fever 20 1.717
117
BNP002 Bone Epithelioid Hemangioma 20 1.717
118
WHT003 White Piedra 18 1.717
119
CHR051 Chorea Gravidarum 16 1.717
120
PRT006 Partial Motor Epilepsy 15 1.717
121
SNL011 Snail Allergy 9 1.717
122
c LKM061 Leukemia, Acute Myeloid 81 1.214
123
ART140 Arteries, Anomalies of 51 1.214
124
NRN002 Neuronitis 43 0.147
125
VRL011 Viral Infectious Disease 64 0.073
126
P PRS040 Prostate Cancer 88 0.052
127
P HPT021 Hepatitis 75 0.052
128
c HPT073 Hepatitis C Virus 73 0.052
129
c HPT001 Hepatitis C 73 0.052
130
LVR012 Liver Cirrhosis 73 0.052
131
PSY004 Psychotic Disorder 72 0.052
132
P MJR001 Major Depressive Disorder 70 0.052
133
GST050 Gastrointestinal System Disease 66 0.052
134
ACQ007 Acquired Immunodeficiency Syndrome 65 0.052
135
P THL005 Thalassemia 65 0.052
136
P ASP006 Aspergillosis 65 0.052
137
MDD011 Mood Disorder 64 0.052
138
FTT001 Fatty Liver Disease 62 0.052
139
MNT002 Mental Depression 60 0.052
140
c ALP101 Alpha-Thalassemia 60 0.052
141
GT001 Gout 60 0.052
142
PRS047 Prostatitis 59 0.052
143
P PLY019 Polyneuropathy 58 0.052
144
NNL002 Nonalcoholic Steatohepatitis 56 0.052
145
SPS003 Spastic Diplegia 55 0.052
146
DBT004 Diabetic Polyneuropathy 51 0.052
147
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.052
148
P VSC018 Visceral Steatosis 38 0.052
149
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.052
150
P RNG031 Ring Chromosome Y Syndrome 29 0.052
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