Search results for f5

135 hits were found for f5

# Family MCID Name MIFTS Score
1
FCT006 Factor V Deficiency 57 4.527
2
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 4.085
3
P BDD001 Budd-Chiari Syndrome 56 3.755
4
STR067 Stroke, Ischemic 75 3.519
5
P THR015 Thrombophilia 59 3.464
6
PRG092 Pregnancy Loss, Recurrent 1 31 2.971
7
c HMP029 Hemophilia a 63 2.927
8
PLM033 Pulmonary Embolism 60 2.927
9
P HMR003 Hemorrhagic Disease 57 2.927
10
P ANT006 Antiphospholipid Syndrome 56 2.927
11
PRT014 Protein S Deficiency 53 2.927
12
PRT011 Protein C Deficiency 52 2.927
13
P HMC002 Homocystinuria 50 2.927
14
HLL004 Hellp Syndrome 50 2.927
15
HYP037 Hyperhomocysteinemia 50 2.927
16
PRT018 Portal Vein Thrombosis 49 2.927
17
PLC007 Placental Abruption 47 2.927
18
PST095 Post-Thrombotic Syndrome 47 2.927
19
THR024 Thrombosis 57 2.666
20
VND001 Vein Disease 47 2.666
21
FCT013 Factor V Leiden Thrombophilia 22 2.666
22
VSC007 Vascular Disease 67 2.644
23
c THR092 Thrombophilia Due to Thrombin Defect 54 2.644
24
CRB132 Cerebral Sinovenous Thrombosis 31 2.644
25
P MYC007 Myocardial Infarction 79 2.618
26
CRB037 Cerebral Palsy 66 2.618
27
VNW001 Von Willebrand's Disease 61 2.618
28
OVR029 Ovarian Hyperstimulation Syndrome 61 2.618
29
LGG001 Legg-Calve-Perthes Disease 57 2.618
30
c ACT210 Acute Respiratory Distress Syndrome 57 2.618
31
c PRC016 Pre-Eclampsia 56 2.618
32
PTN001 Patent Foramen Ovale 55 2.618
33
P HYP620 Hypoprothrombinemia 54 2.618
34
P ECL001 Eclampsia 54 2.618
35
THR016 Thrombophlebitis 53 2.618
36
DSS009 Disseminated Intravascular Coagulation 51 2.618
37
FCT004 Factor Xii Deficiency 50 2.618
38
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 2.618
39
c SVR005 Severe Pre-Eclampsia 49 2.618
40
P DYS026 Dysfibrinogenemia 45 2.618
41
FCT005 Factor Xiii Deficiency 43 2.618
42
P RTN022 Retinal Vein Occlusion 38 2.618
43
c CNT016 Central Retinal Vein Occlusion 36 2.618
44
HMC014 Homocysteinemia 35 2.618
45
PLC008 Placenta Disease 33 2.618
46
RTN021 Retinal Vascular Occlusion 32 2.618
47
BLD072 Bleeding Disorder, East Texas Type 16 2.296
48
FCT017 Factor V Cambridge Thrombophilia 7 2.296
49
c F5R001 F5-Related Budd-Chiari Syndrome 5 2.296
50
FCT018 Factor V R2 Mutation Thrombophilia 4 2.296
51
FCT003 Factor X Deficiency 61 2.268
52
P INT068 Intestinal Disease 60 2.268
53
P HMP007 Hemophilia 57 2.268
54
SCT005 Scott Syndrome 53 2.268
55
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 2.268
56
P SCH018 Schizencephaly 52 2.268
57
P PRC031 Preeclampsia/eclampsia 1 51 2.268
58
INT075 Intracranial Hypertension 50 2.268
59
QBC001 Quebec Platelet Disorder 48 2.268
60
P AFB001 Afibrinogenemia 48 2.268
61
P PRN026 Porencephaly 48 2.268
62
PRP007 Priapism 46 2.268
63
SPS007 Spastic Cerebral Palsy 44 2.268
64
c HMG003 Hemoglobin E Disease 44 2.268
65
P RTN014 Retinal Artery Occlusion 44 2.268
66
CRT015 Carotid Artery Occlusion 43 2.268
67
c SVR056 Severe Hemophilia a 43 2.268
68
c ACQ014 Acquired Hemophilia 42 2.268
69
CTS005 Catastrophic Antiphospholipid Syndrome 42 2.268
70
MDS022 Mediastinitis 41 2.268
71
EBL001 Ebola Hemorrhagic Fever 40 2.268
72
c ACQ042 Acquired Hemophilia a 40 2.268
73
c ACQ012 Acquired Angioedema 39 2.268
74
ISC015 Ischemic Colitis 39 2.268
75
MNN021 Meningococcemia 39 2.268
76
AMR003 Amaurosis Fugax 38 2.268
77
PRP028 Peripheral Vertigo 38 2.268
78
INT078 Intracranial Thrombosis 36 2.268
79
SGT001 Sagittal Sinus Thrombosis 35 2.268
80
SPN185 Spinal Cord Infarction 34 2.268
81
ALV006 Alveolar Capillary Dysplasia 33 2.268
82
FCT016 Factor V and Factor Viii, Combined Deficiency of 33 2.268
83
LVD002 Livedoid Vasculopathy 32 2.268
84
ACN019 Acanthamoeba Keratitis 32 2.268
85
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 2.268
86
SDD008 Sudden Sensorineural Hearing Loss 31 2.268
87
INF133 Inferior Vena Cava Interruption 29 2.268
88
PRC051 Paracetamol Poisoning 27 2.268
89
MYT019 May-Thurner Syndrome 23 2.268
90
MTH044 Mthfr Gene Mutation 21 2.268
91
CRB039 Cerebrovascular Disease 63 1.851
92
BHC003 Behcet Syndrome 60 1.851
93
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 43 1.851
94
STC016 Sticky Platelet Syndrome 29 1.851
95
P MDL005 Medulloblastoma 77 0.093
96
TST021 Testicular Germ Cell Tumor 69 0.093
97
EWN003 Ewing Sarcoma 66 0.093
98
MLN008 Melanoma 62 0.093
99
P NRV006 Nervous System Cancer 60 0.093
100
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.093
101
NRN004 Neuroendocrine Tumor 56 0.093
102
CRC006 Carcinoid Syndrome 52 0.093
103
LKC003 Leukocyte Disease 43 0.093
104
CLV009 Clove Syndrome, Somatic 41 0.093
105
GRM001 Germ Cell and Embryonal Cancer 36 0.093
106
SKN019 Skin Melanoma 62 0.076
107
SKN023 Skin Tag 44 0.076
108
P SKN013 Skin Benign Neoplasm 43 0.076
109
P BRS047 Breast Cancer 100 0.053
110
P OBS005 Obesity 92 0.053
111
PCK002 Pick Disease 68 0.053
112
GLN010 Glanzmann Thrombasthenia 63 0.053
113
OCL009 Ocular Cancer 59 0.053
114
VRL011 Viral Infectious Disease 55 0.053
115
OPT006 Optic Nerve Disease 52 0.053
116
OCL022 Ocular Melanoma 52 0.053
117
P RNL017 Renal Oncocytoma 47 0.053
118
GST009 Gastroschisis 47 0.053
119
PRP021 Peripheral Nervous System Neoplasm 46 0.053
120
INC022 Inclusion-Cell Disease 46 0.053
121
c CLL013 Cell Type Cancer 46 0.053
122
SNS023 Sensory System Cancer 43 0.053
123
MCS004 Mucosal Melanoma 41 0.053
124
MLN013 Melanoma Metastasis 40 0.053
125
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.053
126
THR035 Thrombasthenia 39 0.053
127
MLG088 Malignant Germ Cell Tumor 38 0.053
128
BLD054 Blood Protein Disease 37 0.053
129
P CNT036 Central Nervous System Germ Cell Tumor 37 0.053
130
OPT008 Optic Nerve Neoplasm 36 0.053
131
FST001 Foster-Kennedy Syndrome 31 0.053
132
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.053
133
c ADL022 Adult Central Nervous System Primitive Neuroectodermal Neoplasm 15 0.053
134
PRM139 Primary Melanoma of the Central Nervous System 15 0.053
135
MLG109 Malignant Melanoma of the Mucosa 10 0.053
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