Search results for vwf

258 hits were found for vwf

# Family MCID Name MIFTS Score
1
P VNW001 Von Willebrand's Disease 65 5.093
2
c VNW010 Von Willebrand Disease, Type 2 50 4.114
3
c VNW005 Von Willebrand Disease, Type 1 48 3.868
4
c VNW008 Von Willebrand Disease, Type 3 46 3.735
5
P BRS047 Breast Cancer 97 2.546
6
P THR005 Thrombotic Thrombocytopenic Purpura 61 2.418
7
PRP027 Peripheral Vascular Disease 71 2.317
8
c SYS001 Systemic Lupus Erythematosus 86 2.298
9
THR024 Thrombosis 57 2.214
10
P THR014 Thrombocytopenia 67 2.194
11
P HML001 Hemolytic-Uremic Syndrome 53 2.137
12
STR067 Stroke, Ischemic 81 2.084
13
PRP030 Purpura 54 2.084
14
P VSC007 Vascular Disease 63 2.069
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 2.053
16
c PRC016 Pre-Eclampsia 63 2.035
17
c ACT075 Acute Myocardial Infarction 57 2.035
18
P ANT006 Antiphospholipid Syndrome 55 2.035
19
c HYP595 Hypertension, Essential 84 2.017
20
P HRT032 Heart Disease 75 2.017
21
P MYC007 Myocardial Infarction 70 2.017
22
P ESS003 Essential Thrombocythemia 68 2.017
23
P BRN019 Bernard-Soulier Syndrome 60 2.017
24
P THR015 Thrombophilia 51 2.017
25
BLD053 Blood Platelet Disease 49 2.017
26
URM002 Uremia 49 2.017
27
MLR004 Malaria 81 1.996
28
P HYP086 Hypothyroidism 69 1.996
29
ANG020 Angiosarcoma 64 1.996
30
P HML002 Hemolytic Anemia 63 1.996
31
P VSC011 Vasculitis 62 1.996
32
P HMR003 Hemorrhagic Disease 53 1.996
33
c HMP029 Hemophilia a 67 1.992
34
P PLM037 Pulmonary Hypertension 67 1.972
35
P ATR011 Atrial Fibrillation 66 1.972
36
AFB002 Afibrinogenemia, Congenital 65 1.972
37
INT002 Intermittent Claudication 61 1.972
38
HLL004 Hellp Syndrome 54 1.972
39
ANG011 Angiodysplasia 43 1.972
40
FCT001 Factor Viii Deficiency 51 1.804
41
c ACQ017 Acquired Von Willebrand Syndrome 49 1.804
42
c PSD048 Pseudo-Von Willebrand Disease 39 1.750
43
ATH013 Atherosclerosis Susceptibility 65 1.735
44
DSS009 Disseminated Intravascular Coagulation 57 1.735
45
RYN005 Raynaud Phenomenon 47 1.702
46
CRB039 Cerebrovascular Disease 67 1.662
47
P CRN300 Coronary Heart Disease 1 63 1.662
48
PRT013 Portal Hypertension 59 1.662
49
P CRD246 Cardiovascular System Disease 57 1.662
50
CRN030 Coronary Stenosis 50 1.662
51
CRN017 Coronary Thrombosis 47 1.662
52
HMR002 Hemarthrosis 45 1.662
53
c ART115 Aortic Valve Disease 1 75 1.638
54
P HYP061 Hypertrophic Cardiomyopathy 70 1.638
55
PLY001 Polycythemia Vera 69 1.638
56
P GLY013 Glycogen Storage Disease 60 1.638
57
GRY002 Gray Platelet Syndrome 59 1.638
58
LMB062 Limb Ischemia 55 1.638
59
c CNT016 Central Retinal Vein Occlusion 53 1.638
60
HMC014 Homocysteinemia 53 1.638
61
PRP080 Peripheral Artery Disease 53 1.638
62
P CLL015 Collagen Disease 47 1.638
63
c DLT002 Dilated Cardiomyopathy 79 1.610
64
P APL001 Aplastic Anemia 74 1.610
65
SCK003 Sickle Cell Anemia 74 1.610
66
P MSC005 Muscular Dystrophy 66 1.610
67
GLN010 Glanzmann Thrombasthenia 66 1.610
68
MYL031 Myeloproliferative Neoplasm 66 1.610
69
P DBT009 Diabetes Mellitus 64 1.610
70
MGK001 Megakaryocytic Leukemia 64 1.610
71
ACT119 Acute Promyelocytic Leukemia 63 1.610
72
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 1.610
73
TKY002 Takayasu Arteritis 62 1.610
74
LPP008 Lipoprotein Quantitative Trait Locus 62 1.610
75
P HMN010 Hemangioma 61 1.610
76
P SCL018 Scoliosis 60 1.610
77
VRC005 Varicose Veins 60 1.610
78
HYD002 Hydronephrosis 60 1.610
79
PLM033 Pulmonary Embolism 59 1.610
80
VSC002 Vascular Dementia 57 1.610
81
PLC005 Placental Insufficiency 57 1.610
82
P VNS003 Venous Insufficiency 55 1.610
83
FCT004 Factor Xii Deficiency 55 1.610
84
ESN011 Eisenmenger Syndrome 55 1.610
85
THR004 Thrombocytosis 51 1.610
86
VSC006 Vascular Cancer 51 1.610
87
SYS003 Systolic Heart Failure 49 1.610
88
SPT005 Spotted Fever 49 1.610
89
INT078 Intracranial Thrombosis 49 1.610
90
HPT009 Hepatopulmonary Syndrome 48 1.610
91
c MLG069 Malignant Hypertension 47 1.610
92
DBT008 Diabetic Angiopathy 44 1.610
93
HYP008 Hypertensive Retinopathy 39 1.610
94
AFR002 African Tick-Bite Fever 37 1.610
95
QLT001 Qualitative Platelet Defect 29 1.610
96
THR123 Thrombotic Microangiopathy 36 1.284
97
ACT058 Active Peptic Ulcer Disease 55 1.248
98
CRT004 Carotid Artery Thrombosis 38 1.227
99
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 1.203
100
c ART101 Aortic Valve Disease 2 65 1.203
101
INT007 Intermediate Coronary Syndrome 55 1.203
102
FCT006 Factor V Deficiency 57 1.175
103
ART140 Arteries, Anomalies of 52 1.175
104
THR016 Thrombophlebitis 51 1.175
105
c ALM001 Al Amyloidosis 50 1.175
106
P BLD051 Blood Coagulation Disease 46 1.175
107
BMB001 Bombay Phenotype 32 1.175
108
c HMP004 Hemophilia B 68 1.139
109
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 1.139
110
P BTH005 Bethlem Myopathy 1 62 1.139
111
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 1.139
112
PTN001 Patent Foramen Ovale 60 1.139
113
FCT002 Factor Xi Deficiency 60 1.139
114
P MYM013 Moyamoya Disease 1 57 1.139
115
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 1.139
116
HRT012 Heart Valve Disease 53 1.139
117
FCT005 Factor Xiii Deficiency 52 1.139
118
CRT016 Carotid Artery Disease 52 1.139
119
P CPL006 Capillary Hemangioma 51 1.139
120
P MTR003 Mitral Valve Stenosis 50 1.139
121
P ART018 Aortic Valve Insufficiency 49 1.139
122
DRG013 Drug-Induced Lupus Erythematosus 48 1.139
123
GNR003 Generalized Atherosclerosis 46 1.139
124
CMP028 Complement Component 2 Deficiency 46 1.139
125
LYM008 Lymphangiosarcoma 45 1.139
126
KPS002 Kaposiform Hemangioendothelioma 43 1.139
127
P VND001 Vein Disease 42 1.139
128
CRD118 Cardiovascular Cancer 41 1.139
129
P INT260 Intracranial Berry Aneurysm 39 1.139
130
c BLD126 Bleeding Disorder, Platelet-Type, 18 39 1.139
131
c PRM225 Primary Thrombocytopenia 39 1.139
132
BLD054 Blood Protein Disease 38 1.139
133
MRN001 Marantic Endocarditis 38 1.139
134
CPL002 Capillary Lymphangioma 37 1.139
135
CPL005 Capillary Disease 36 1.139
136
c GRS012 Griscelli Syndrome, Type 3 36 1.139
137
SPL009 Splenic Sequestration 35 1.139
138
P HPT020 Hepatic Vascular Disease 34 1.139
139
PLT015 Platelet Aggregation, Spontaneous 34 1.139
140
c BRC062 Brachydactyly, Type D 34 1.139
141
c CRB170 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2 34 1.139
142
PLM180 Pulmonary Artery Disease 33 1.139
143
PDT004 Pediatric Angiosarcoma 31 1.139
144
c CLR080 Colorectal Cancer 5 31 1.139
145
FNT004 Fainting 30 1.139
146
c INH004 Inherited Blood Coagulation Disease 30 1.139
147
INF011 Infiltrating Angiolipoma 28 1.139
148
CRD007 Cardiovascular Organ Benign Neoplasm 27 1.139
149
XLN228 X-Linked Recessive Disease 26 1.139
150
PPL016 Papillary Adenofibroma 26 1.139
151
THY004 Thyroid Angiosarcoma 26 1.139
152
CRT001 Carotid Body Cancer 25 1.139
153
MDD004 Middle Ear Adenocarcinoma 24 1.139
154
c ATM013 Autoimmune Disease of Cardiovascular System 24 1.139
155
END074 Endocardium Disease 22 1.139
156
MDL001 Medulloadrenal Hyperfunction 22 1.139
157
UNL013 Unilateral Absence of a Pulmonary Artery 20 1.139
158
P HMP007 Hemophilia 51 0.242
159
c THR092 Thrombophilia Due to Thrombin Defect 73 0.125
160
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.117
161
c MCR113 Microvascular Complications of Diabetes 3 52 0.108
162
c MCR120 Microvascular Complications of Diabetes 7 47 0.108
163
c ACQ014 Acquired Hemophilia 45 0.108
164
c MCR130 Microvascular Complications of Diabetes 6 41 0.108
165
c MCR133 Microvascular Complications of Diabetes 4 41 0.108
166
ISC004 Ischemia 58 0.099
167
LVR012 Liver Cirrhosis 62 0.088
168
CRB004 Cerebral Artery Occlusion 45 0.088
169
HYP266 Hypoxia 57 0.076
170
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.076
171
P KDN018 Kidney Disease 72 0.062
172
MYL009 Myelodysplastic Syndrome 70 0.062
173
ADL002 Adult Syndrome 70 0.062
174
P SYS005 Systemic Scleroderma 68 0.062
175
CNN005 Connective Tissue Disease 68 0.062
176
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.062
177
c SCL052 Scleroderma, Familial Progressive 61 0.062
178
P GLM007 Glomerulonephritis 57 0.062
179
HMT008 Hematuria, Benign Familial 56 0.062
180
PLM010 Pulmonary Edema 54 0.062
181
MCR004 Macroglobulinemia 49 0.062
182
c CHR682 Chronic Bilirubin Encephalopathy 39 0.062
183
c CNG388 Congenital Disorder of Glycosylation, Type Iw 27 0.062
184
P OVR042 Ovarian Cancer 88 0.044
185
IMM167 Immune Deficiency Disease 78 0.044
186
P LNG064 Lung Cancer Susceptibility 3 78 0.044
187
CRV035 Cervical Cancer 76 0.044
188
c ATR087 Atrial Standstill 1 75 0.044
189
c HYP836 Hypercholesterolemia, Familial, 1 73 0.044
190
ULC004 Ulcerative Colitis 73 0.044
191
P CNR004 Cone-Rod Dystrophy 2 73 0.044
192
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.044
193
P GRF003 Graft-Versus-Host Disease 72 0.044
194
P AMY004 Amyloidosis 70 0.044
195
MYL005 Myelofibrosis 70 0.044
196
c CHR684 Chronic Kidney Disease 70 0.044
197
CRT072 Creutzfeldt-Jakob Disease 70 0.044
198
RCK004 Rickets 68 0.044
199
P HPT021 Hepatitis 67 0.044
200
LPT001 Leptospirosis 66 0.044
201
ANG054 Angina Pectoris 66 0.044
202
P MCR115 Microvascular Complications of Diabetes 5 66 0.044
203
c MCR129 Microvascular Complications of Diabetes 1 66 0.044
204
P HYD006 Hydrocephalus 66 0.044
205
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.044
206
P ADN016 Adenocarcinoma 64 0.044
207
c HPT001 Hepatitis C 62 0.044
208
P ART023 Arthropathy 62 0.044
209
CHL068 Cholestasis 61 0.044
210
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.044
211
RHM001 Rheumatic Fever 60 0.044
212
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.044
213
c ACT071 Acute Kidney Failure 60 0.044
214
THY029 Thyroid Carcinoma 59 0.044
215
HLC007 Helicobacter Pylori Infection 59 0.044
216
PPT005 Peptic Ulcer Disease 59 0.044
217
c ACT073 Acute Leukemia 58 0.044
218
BLR008 Bilirubin Metabolic Disorder 57 0.044
219
SCH014 Schistosomiasis 57 0.044
220
P PLY018 Polycythemia 56 0.044
221
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.044
222
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.044
223
P HYP076 Hyperthyroidism 55 0.044
224
P ART021 Arteriosclerosis 54 0.044
225
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.044
226
RHM028 Rheumatic Heart Disease 53 0.044
227
P HYP083 Hypopituitarism 53 0.044
228
PRN011 Pernicious Anemia 53 0.044
229
P RTN022 Retinal Vein Occlusion 53 0.044
230
P INT068 Intestinal Disease 53 0.044
231
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.044
232
P ACT105 Acute Mountain Sickness 52 0.044
233
P OVR049 Ovarian Disease 52 0.044
234
c ACT135 Acute Graft Versus Host Disease 52 0.044
235
ALK024 Alkuraya-Kucinskas Syndrome 51 0.044
236
CLR109 Colorectal Adenocarcinoma 51 0.044
237
P ECL001 Eclampsia 50 0.044
238
c SVR005 Severe Pre-Eclampsia 50 0.044
239
HMG002 Hemoglobinuria 50 0.044
240
47X002 47,xyy 49 0.044
241
BRN071 Brain Injury 49 0.044
242
VCC001 Vaccinia 49 0.044
243
BNR002 Bone Resorption Disease 48 0.044
244
ATS010 Autosomal Recessive Disease 48 0.044
245
MSN004 Mesenchymal Cell Neoplasm 41 0.044
246
c MCR112 Microvascular Complications of Diabetes 2 41 0.044
247
P DYS005 Dyslexia 40 0.044
248
ASP030 Aspirin Resistance 39 0.044
249
48X005 48,xyyy 39 0.044
250
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.044
251
SCR011 Scrapie 39 0.044
252
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.044
253
MLD002 Mild Pre-Eclampsia 36 0.044
254
MBM001 Meibomian Cyst 35 0.044
256
CNG506 Congenital Amyoplasia 27 0.044
257
ARG004 Argyria 27 0.044
258
P PLT029 Platelet Groups--Ko System 16 0.044
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