Search results for Von Willebrand Factor Human

823 hits were found for Von Willebrand Factor Human

# Family MCID Name MIFTS Score
1
P VNW001 Von Willebrand's Disease 64 1.437
2
P HMP007 Hemophilia 51 0.624
3
FCT001 Factor Viii Deficiency 55 0.519
4
PRP030 Purpura 55 0.518
5
IMM167 Immune Deficiency Disease 78 0.515
6
c HMP029 Hemophilia a 65 0.504
7
c ACQ017 Acquired Von Willebrand Syndrome 49 0.490
8
P CLR023 Colorectal Cancer 98 0.468
9
P BRS047 Breast Cancer 96 0.462
10
P THR014 Thrombocytopenia 68 0.458
11
INS024 Insulin-Like Growth Factor I 79 0.447
12
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.438
13
P VSC007 Vascular Disease 63 0.437
14
ATH013 Atherosclerosis Susceptibility 66 0.430
15
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.422
16
THR024 Thrombosis 56 0.422
17
P ADN016 Adenocarcinoma 64 0.410
18
P GLM045 Glioma 63 0.388
19
VNH007 Von Hippel-Lindau Syndrome 73 0.381
20
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.377
21
ATM095 Autoimmune Disease 61 0.377
22
GLL048 Glial Tumor 45 0.376
23
P LNG032 Lung Cancer 97 0.375
24
P OVR042 Ovarian Cancer 89 0.372
25
P LKM002 Leukemia 66 0.366
26
P CRN300 Coronary Heart Disease 1 63 0.364
27
GLB015 Glioblastoma Multiforme 75 0.361
28
LVR012 Liver Cirrhosis 63 0.359
29
c THR092 Thrombophilia Due to Thrombin Defect 73 0.358
30
P KDN018 Kidney Disease 70 0.357
31
P HPT023 Hepatocellular Carcinoma 100 0.356
32
c PRC016 Pre-Eclampsia 63 0.355
33
HYP266 Hypoxia 56 0.349
34
P NRB001 Neuroblastoma 71 0.347
35
P LYM031 Lymphocytic Leukemia 55 0.336
36
ADN018 Adenoma 58 0.330
37
c VNW005 Von Willebrand Disease, Type 1 49 0.329
38
CRV035 Cervical Cancer 76 0.328
39
OST159 Osteogenic Sarcoma 66 0.328
40
c SYS001 Systemic Lupus Erythematosus 86 0.327
41
P PNC035 Pancreatic Cancer 84 0.324
42
P LVR013 Liver Disease 68 0.322
43
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.320
44
ISC004 Ischemia 60 0.319
45
P PRS040 Prostate Cancer 97 0.316
46
P BLD134 Bladder Cancer 78 0.315
47
P GST053 Gastric Cancer 83 0.314
48
P HRT032 Heart Disease 75 0.313
49
HLX001 Helix Syndrome 47 0.313
50
CYT002 Cytokine Deficiency 44 0.312
51
MLN008 Melanoma 69 0.308
52
48X005 48,xyyy 39 0.305
53
c VNW010 Von Willebrand Disease, Type 2 51 0.304
54
c HYP836 Hypercholesterolemia, Familial, 1 72 0.301
55
P HYP086 Hypothyroidism 68 0.301
56
P DRR001 Diarrhea 57 0.296
57
STR067 Stroke, Ischemic 80 0.296
58
MYL069 Myeloma, Multiple 85 0.291
59
CRB039 Cerebrovascular Disease 69 0.289
60
P LYM118 Lymphoma 68 0.289
61
P CRN018 Coronary Artery Anomaly 63 0.287
62
P NTR004 Neutropenia 63 0.286
63
P MCR115 Microvascular Complications of Diabetes 5 66 0.284
64
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.282
65
END030 End Stage Renal Failure 58 0.280
66
LNG099 Lung Disease 61 0.279
67
ACQ007 Acquired Immunodeficiency Syndrome 60 0.278
68
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.278
69
ART140 Arteries, Anomalies of 53 0.272
70
P LPS004 Lupus Erythematosus 61 0.271
71
P MYL006 Myeloid Leukemia 60 0.270
72
P INF037 Inflammatory Bowel Disease 56 0.269
73
LPD008 Lipid Metabolism Disorder 62 0.267
74
c ACT075 Acute Myocardial Infarction 56 0.266
75
P HML001 Hemolytic-Uremic Syndrome 52 0.265
76
P MYC007 Myocardial Infarction 70 0.265
77
c SML038 Small Cell Cancer of the Lung 65 0.264
78
c CHR684 Chronic Kidney Disease 66 0.264
79
P PRD008 Periodontitis 62 0.264
80
PRT037 Pertussis 65 0.261
81
TXC005 Toxic Shock Syndrome 61 0.260
82
P VSC011 Vasculitis 62 0.258
83
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.256
84
CNG034 Congestive Heart Failure 70 0.256
85
P AST007 Astrocytoma 50 0.255
86
P ATR011 Atrial Fibrillation 66 0.254
87
c HYP595 Hypertension, Essential 84 0.252
88
P PLM037 Pulmonary Hypertension 68 0.252
89
P GLM007 Glomerulonephritis 57 0.251
90
PRP027 Peripheral Vascular Disease 71 0.250
91
c LKM061 Leukemia, Acute Myeloid 83 0.250
92
P HRP006 Herpes Simplex 65 0.249
93
DFC004 Deficiency Anemia 75 0.249
94
P ALZ034 Alzheimer Disease 88 0.248
95
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.247
96
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.247
97
P RHM011 Rheumatoid Arthritis 80 0.246
98
P DBT009 Diabetes Mellitus 64 0.245
100
HYP066 Hyperglycemia 61 0.242
101
P CRD246 Cardiovascular System Disease 56 0.241
102
P LKM062 Leukemia, Acute Lymphoblastic 68 0.240
103
c MCR113 Microvascular Complications of Diabetes 3 52 0.239
104
AGN016 Aging 56 0.238
105
c MCR120 Microvascular Complications of Diabetes 7 47 0.238
106
c HMP004 Hemophilia B 67 0.238
107
c MCR130 Microvascular Complications of Diabetes 6 41 0.238
108
c MCR133 Microvascular Complications of Diabetes 4 41 0.238
109
47X002 47,xyy 49 0.236
110
ANR040 Aneurysm 58 0.233
111
OST012 Osteoarthritis 78 0.231
112
CRH001 Crohn's Disease 74 0.229
113
MLR004 Malaria 80 0.228
114
KPS004 Kaposi Sarcoma 75 0.227
115
P END044 Endometriosis 62 0.225
116
BNR002 Bone Resorption Disease 48 0.225
117
IRN002 Iron Metabolism Disease 57 0.221
118
ALL026 Allergic Hypersensitivity Disease 64 0.221
119
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.221
120
CHL014 Cholera 55 0.220
121
P ECL001 Eclampsia 51 0.220
122
P HMR003 Hemorrhagic Disease 52 0.220
123
ANG011 Angiodysplasia 43 0.220
124
P HML002 Hemolytic Anemia 62 0.220
125
SPP010 Suppressor of Tumorigenicity 3 51 0.219
126
THR123 Thrombotic Microangiopathy 38 0.218
127
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.218
128
P BCL017 B-Cell Lymphoma 58 0.218
129
SRC014 Sarcoma 65 0.217
130
HMN009 Hemangioblastoma 54 0.217
131
c SCL052 Scleroderma, Familial Progressive 62 0.217
132
P GRF003 Graft-Versus-Host Disease 71 0.217
133
IDP011 Idiopathic Interstitial Pneumonia 63 0.215
134
P PLM036 Pulmonary Fibrosis 61 0.214
135
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.214
136
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.214
137
DPR016 Depression 63 0.214
138
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.214
139
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.214
140
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.214
141
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.214
142
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.214
143
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.214
144
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.214
145
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.214
146
c HPT001 Hepatitis C 63 0.214
147
ULC004 Ulcerative Colitis 73 0.214
148
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.212
149
P ENC004 Encephalitis 61 0.210
150
BCT022 Bacterial Infectious Disease 56 0.210
151
DSS009 Disseminated Intravascular Coagulation 57 0.209
152
P RSP003 Respiratory Failure 74 0.209
153
PLM033 Pulmonary Embolism 59 0.208
154
c LKM071 Leukemia, Chronic Lymphocytic 79 0.208
155
SPN035 Spindle Cell Sarcoma 51 0.208
156
ALC007 Alcohol Dependence 66 0.208
157
P THR015 Thrombophilia 50 0.207
158
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.206
159
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.205
160
P SKN015 Skin Carcinoma 67 0.204
161
OCL069 Ocular Motor Apraxia 51 0.204
162
BRN071 Brain Injury 49 0.203
163
MYL009 Myelodysplastic Syndrome 70 0.203
164
SKN016 Skin Disease 63 0.203
165
PRT013 Portal Hypertension 60 0.203
166
PRS045 Prostatic Hypertrophy 52 0.202
167
P NRP001 Neuropathy 56 0.200
168
DRM006 Dermatitis 61 0.199
169
c ATR087 Atrial Standstill 1 74 0.196
170
TLN003 Telangiectasis 51 0.195
171
INT007 Intermediate Coronary Syndrome 55 0.194
172
THR004 Thrombocytosis 51 0.193
173
GST045 Gastroenteritis 59 0.192
174
c RRH015 Rare Hemorrhagic Disorder 23 0.192
175
P ALC033 Alcohol Use Disorder 58 0.192
176
P PLY018 Polycythemia 55 0.192
177
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.192
178
DWN001 Down Syndrome 70 0.192
179
P ART021 Arteriosclerosis 54 0.191
180
P ART023 Arthropathy 62 0.190
181
c ACT073 Acute Leukemia 58 0.189
182
P AMY004 Amyloidosis 70 0.189
183
TRM010 Traumatic Brain Injury 53 0.189
184
c ACT071 Acute Kidney Failure 59 0.189
185
ANG054 Angina Pectoris 66 0.188
186
MNN042 Meningioma, Radiation-Induced 62 0.187
187
CLR030 Clear Cell Renal Cell Carcinoma 53 0.186
188
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.185
189
c PRM038 Primary Agammaglobulinemia 43 0.185
190
THR035 Thrombasthenia 41 0.185
191
P END033 Endocarditis 57 0.183
192
VCC001 Vaccinia 49 0.183
193
P MLT020 Multiple Sclerosis 72 0.183
194
MNT002 Mental Depression 57 0.183
195
LYM133 Lymphoma, Hodgkin, Classic 69 0.183
196
SCH014 Schistosomiasis 56 0.182
197
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.182
198
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.182
199
c LKM063 Leukemia, Chronic Myeloid 71 0.181
200
P ART022 Arthritis 70 0.181
201
P BRN019 Bernard-Soulier Syndrome 60 0.181
202
ART016 Aortic Aneurysm 68 0.181
203
CLT003 Colitis 62 0.181
204
SPN021 Spinal Meningioma 47 0.181
205
c WLM018 Wilms Tumor 5 62 0.181
206
c MNN043 Meningioma, Familial 74 0.181
207
SCR001 Secretory Meningioma 37 0.180
208
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.180
209
AST005 Asthma 77 0.180
210
P NPH012 Nephrotic Syndrome 63 0.179
211
P FBR017 Fibrosarcoma 56 0.179
212
BCK006 Back Pain 42 0.179
213
RTN017 Retinal Detachment 60 0.178
214
c ACT027 Acute Pancreatitis 59 0.178
215
c PSD048 Pseudo-Von Willebrand Disease 41 0.178
216
P BPL003 Bipolar Disorder 56 0.178
217
c SPN225 Spondyloarthropathy 1 73 0.178
218
P GST044 Gastritis 55 0.177
219
c HPT003 Hepatitis a 63 0.176
220
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.176
221
c MJR024 Major Affective Disorder 9 41 0.176
222
c MJR022 Major Affective Disorder 8 38 0.176
223
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.176
224
c VRL010 Viral Hepatitis 51 0.176
225
P SCK005 Sickle Cell Disease 50 0.176
226
P SYS005 Systemic Scleroderma 70 0.175
227
P HYP076 Hyperthyroidism 55 0.175
228
P MYP004 Myopathy 64 0.175
229
P DMN002 Dementia 67 0.175
230
HYP060 Hyperinsulinism 54 0.174
231
CYS001 Cystic Fibrosis 80 0.174
232
P HMN010 Hemangioma 61 0.173
233
P THY032 Thyroiditis 53 0.173
234
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.172
235
HDN002 Head Injury 45 0.171
236
c DLT002 Dilated Cardiomyopathy 79 0.171
237
P MSC005 Muscular Dystrophy 66 0.170
238
P ANT006 Antiphospholipid Syndrome 54 0.170
239
CNN005 Connective Tissue Disease 66 0.169
240
c MGR028 Migraine with or Without Aura 1 69 0.169
241
CYT008 Cytomegalovirus Infection 56 0.169
242
VRC005 Varicose Veins 60 0.169
243
PRT036 Peritonitis 65 0.166
244
P SZR006 Seizure Disorder 58 0.166
245
c ART101 Aortic Valve Disease 2 63 0.165
246
P HDC001 Headache 57 0.164
247
P CRD119 Cardiac Arrest 67 0.164
248
HRW001 Hair Whorl 36 0.163
249
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.163
250
URM002 Uremia 49 0.162
251
ADL002 Adult Syndrome 69 0.162
252
P HYP750 Hypertriglyceridemia, Familial 61 0.162
253
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.162
254
P ATX030 Ataxia-Telangiectasia 83 0.160
255
P THL005 Thalassemia 60 0.159
256
ERY051 Erythroleukemia, Familial 56 0.159
257
FCT007 Factor Vii Deficiency 66 0.159
258
P ESS003 Essential Thrombocythemia 67 0.159
259
HMC014 Homocysteinemia 53 0.159
260
P GRV001 Graves' Disease 55 0.159
261
P HYP069 Hyperparathyroidism 62 0.159
262
VSL002 Visual Epilepsy 58 0.158
263
c ACT134 Acute Liver Failure 51 0.157
264
PLY001 Polycythemia Vera 69 0.157
265
SPL018 Splenomegaly 48 0.157
266
P HPT021 Hepatitis 67 0.156
267
RRS014 Rare Surgical Neurologic Disease 32 0.156
268
ANT024 Anthrax Disease 58 0.156
269
CHR178 Chromosomal Triplication 35 0.156
270
c BRN108 Branchiootic Syndrome 1 61 0.156
271
VRL011 Viral Infectious Disease 61 0.155
272
BRN024 Bronchitis 68 0.155
273
P DNG005 Dengue Virus 57 0.154
274
P PLY011 Polycystic Ovary Syndrome 56 0.154
275
P SCL018 Scoliosis 60 0.154
276
P HYP061 Hypertrophic Cardiomyopathy 66 0.153
277
CRB004 Cerebral Artery Occlusion 44 0.153
278
FCT002 Factor Xi Deficiency 59 0.152
279
SPN051 Spondylitis 52 0.151
280
P UVT001 Uveitis 57 0.151
281
INF009 Inflammatory Spondylopathy 32 0.151
282
PLM010 Pulmonary Edema 55 0.149
283
RHM027 Rheumatic Disease 56 0.149
284
P MNN013 Meningitis 65 0.148
285
GST040 Gastric Adenocarcinoma 70 0.148
286
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.147
287
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.147
288
PNG002 Pain Agnosia 51 0.147
289
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 54 0.147
290
P TRN020 Turner Syndrome 65 0.147
291
CHC001 Chickenpox 60 0.147
292
IGG001 Iga Glomerulonephritis 48 0.147
293
GLC003 Glucose Intolerance 54 0.145
294
PPT005 Peptic Ulcer Disease 58 0.144
295
ANR007 Anorexia Nervosa 63 0.144
296
ACT058 Active Peptic Ulcer Disease 55 0.144
297
CNS004 Constipation 57 0.143
298
TRN015 Transient Cerebral Ischemia 62 0.143
299
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.143
300
FCT005 Factor Xiii Deficiency 53 0.142
301
c ACT135 Acute Graft Versus Host Disease 51 0.142
302
P OPN001 Open-Angle Glaucoma 49 0.142
303
P PRP019 Peripheral Nervous System Disease 57 0.142
304
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.141
305
P PRS038 Personality Disorder 65 0.141
306
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.140
307
P GLY013 Glycogen Storage Disease 59 0.140
308
GNG013 Gingivitis 59 0.139
309
P SRC025 Sarcoidosis 1 70 0.139
310
MYL031 Myeloproliferative Neoplasm 65 0.138
311
c MCR129 Microvascular Complications of Diabetes 1 66 0.138
312
PLC008 Placenta Disease 49 0.138
313
P MYP006 Myopia 55 0.138
314
SYN007 Synovitis 55 0.138
315
MCL006 Macular Retinal Edema 55 0.137
316
c ACQ014 Acquired Hemophilia 45 0.136
317
RYN005 Raynaud Phenomenon 46 0.136
318
INT066 Interstitial Lung Disease 59 0.136
319
HMR002 Hemarthrosis 45 0.135
320
c THR082 Thrombophilia Due to Activated Protein C Resistance 60 0.135
321
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.135
322
PLT015 Platelet Aggregation, Spontaneous 37 0.135
323
FCT004 Factor Xii Deficiency 54 0.135
324
IRN001 Iron Deficiency Anemia 58 0.135
325
ATS010 Autosomal Recessive Disease 48 0.134
326
OST003 Osteonecrosis 61 0.133
327
c SVR005 Severe Pre-Eclampsia 49 0.133
328
c MCR112 Microvascular Complications of Diabetes 2 41 0.132
329
RRD056 Rare Disease in Surgical Orthopedic 28 0.132
330
P ALP008 Alopecia 56 0.132
331
GLN010 Glanzmann Thrombasthenia 66 0.132
332
P LMY004 Leiomyosarcoma 62 0.131
333
INF034 Infective Endocarditis 52 0.131
334
P BRS044 Breast Adenocarcinoma 59 0.131
335
ALL014 Allergic Encephalomyelitis 39 0.130
336
CRT013 Carotid Stenosis 50 0.130
337
MYL005 Myelofibrosis 67 0.130
338
P PLY014 Polycystic Kidney Disease 59 0.130
339
P LYM033 Lymphoproliferative Syndrome 60 0.129
340
HRT012 Heart Valve Disease 53 0.128
341
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.128
342
P PLY019 Polyneuropathy 56 0.127
343
c GLC092 Glaucoma, Primary Open Angle 62 0.127
344
MCS002 Mucositis 55 0.127
345
ACT119 Acute Promyelocytic Leukemia 63 0.127
346
P MMB011 Membranous Nephropathy 50 0.126
347
CRN017 Coronary Thrombosis 47 0.126
348
P PRM006 Primary Biliary Cirrhosis 61 0.126
349
P ART005 Arteriovenous Malformation 65 0.126
350
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.126
351
P ADL010 Adult Respiratory Distress Syndrome 63 0.125
352
FCT006 Factor V Deficiency 56 0.125
353
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.124
354
c MTR002 Mitral Valve Insufficiency 47 0.124
355
BLD053 Blood Platelet Disease 51 0.124
356
ECT026 Ectopic Pregnancy 49 0.123
357
BRN056 Bronchopulmonary Dysplasia 57 0.122
358
INS001 Insulinoma 60 0.121
359
c PRD040 Periodontitis, Chronic 54 0.121
360
ANG020 Angiosarcoma 58 0.120
361
CLF001 Cleft Lip 53 0.120
362
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.120
363
GRW007 Growth Hormone Deficiency 43 0.120
364
PLS007 Plasmodium Falciparum Malaria 52 0.120
365
HRT011 Heart Septal Defect 50 0.119
366
P DRM010 Dermatomyositis 61 0.119
367
P BLD051 Blood Coagulation Disease 46 0.119
368
BRR014 Barrett Esophagus 64 0.118
369
FCT003 Factor X Deficiency 55 0.116
370
NNL006 Non-Alcoholic Steatohepatitis 51 0.116
371
PLC007 Placental Abruption 48 0.116
372
P ART018 Aortic Valve Insufficiency 53 0.116
373
MCR004 Macroglobulinemia 50 0.115
374
P ESP024 Esophagitis 62 0.115
375
c DNG003 Dengue Disease 59 0.115
376
EWN003 Ewing Sarcoma 68 0.115
377
c JVN010 Juvenile Rheumatoid Arthritis 67 0.115
378
OVR029 Ovarian Hyperstimulation Syndrome 63 0.115
379
P VNT002 Ventricular Septal Defect 60 0.114
380
BRS051 Breast Disease 58 0.114
381
P RTN022 Retinal Vein Occlusion 52 0.114
382
P URT039 Urticaria 58 0.113
383
ART002 Arts Syndrome 63 0.113
384
BLR008 Bilirubin Metabolic Disorder 57 0.112
385
P OLG002 Oligodendroglioma 67 0.112
386
P LRY044 Larynx Cancer 54 0.112
387
c WLM013 Wilms Tumor 1 65 0.112
388
P OVR046 Ovarian Cyst 45 0.112
389
STT001 Status Epilepticus 59 0.112
390
P ORT004 Orthostatic Intolerance 63 0.112
391
PRP080 Peripheral Artery Disease 53 0.111
392
PLS011 Plasmacytoma 56 0.111
393
ISL001 Islet Cell Tumor 56 0.109
394
CHR005 Chorioamnionitis 51 0.109
395
CRN030 Coronary Stenosis 50 0.109
396
AFB002 Afibrinogenemia, Congenital 65 0.109
397
VSC002 Vascular Dementia 57 0.109
398
P MST009 Mastocytosis 63 0.109
399
KWS002 Kawasaki Disease 64 0.109
400
P PTN014 Patent Ductus Arteriosus 1 60 0.109
401
CNT047 Contact Dermatitis 57 0.109
402
P TMP003 Temporal Arteritis 67 0.109
403
DBT010 Diabetic Neuropathy 55 0.108
404
P CNR004 Cone-Rod Dystrophy 2 71 0.107
406
HSH003 Hashimoto Thyroiditis 62 0.107
407
HPT004 Hepatic Coma 43 0.106
408
SCK003 Sickle Cell Anemia 72 0.106
409
P CLC063 Celiac Disease 1 68 0.106
410
CRH005 Crohn's Colitis 52 0.106
411
PNC001 Pancytopenia 54 0.105
412
PRN011 Pernicious Anemia 52 0.105
413
P HYP083 Hypopituitarism 53 0.105
414
HMP001 Hemopericardium 46 0.104
415
c RHB024 Rhabdomyosarcoma 2 65 0.103
416
CHL122 Cholesteatoma of Middle Ear 51 0.103
417
P GND004 Gonadal Dysgenesis 49 0.103
418
THY030 Thyroid Gland Disease 51 0.103
419
PST092 Posttransplant Acute Limbic Encephalitis 29 0.103
420
ACN002 Acanthosis Nigricans 60 0.102
421
P INT068 Intestinal Disease 52 0.102
422
P PRL003 Proliferative Glomerulonephritis 44 0.102
423
SYN036 Syncope 45 0.102
424
P DBT005 Diabetes Insipidus 55 0.102
425
c PRM005 Primary Hyperparathyroidism 58 0.102
426
HPT046 Hepatic Veno-Occlusive Disease 56 0.102
427
DNG002 Dengue Hemorrhagic Fever 60 0.102
428
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.101
429
P GCH001 Gaucher's Disease 64 0.101
430
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.101
431
HLL004 Hellp Syndrome 53 0.101
432
c BCT007 Bacterial Meningitis 55 0.101
433
PPL052 Papillomatosis, Confluent and Reticulated 34 0.100
434
P ANR048 Aniridia 1 63 0.100
435
PRT018 Portal Vein Thrombosis 50 0.100
436
BRN004 Brain Edema 55 0.100
437
CNN003 Conn's Syndrome 79 0.099
438
HPT019 Hepatic Encephalopathy 60 0.099
439
INT030 Intracranial Aneurysm 56 0.099
440
c ALM001 Al Amyloidosis 50 0.099
441
CLF004 Cleft Lip/palate 54 0.098
442
P PRC019 Precocious Puberty 47 0.098
443
P PRC012 Pericardial Effusion 51 0.097
444
AND002 Androgen Insensitivity Syndrome 66 0.097
445
SPT005 Spotted Fever 49 0.097
446
P MTR003 Mitral Valve Stenosis 50 0.097
447
P PLY041 Polymyositis 57 0.096
448
HML018 Homologous Wasting Disease 22 0.096
449
PRT014 Protein S Deficiency 50 0.096
450
HYD002 Hydronephrosis 59 0.096
451
P ANG001 Angelman Syndrome 67 0.095
452
HMG005 Hemoglobinopathy 55 0.095
453
c BTT014 Beta-Thalassemia 72 0.095
454
INT002 Intermittent Claudication 61 0.095
455
PRS047 Prostatitis 56 0.094
456
c CNT016 Central Retinal Vein Occlusion 49 0.094
457
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.093
458
P ATR005 Atrophic Gastritis 50 0.093
459
ESP002 Esophageal Varix 51 0.092
460
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.092
461
EPD015 Epidemic Typhus 46 0.092
462
c ANM038 Anemia, Autoimmune Hemolytic 61 0.092
463
c GCH015 Gaucher Disease, Type I 70 0.092
464
DCB001 Decubitus Ulcer 60 0.092
465
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.092
466
CRD137 Cardiogenic Shock 48 0.091
467
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.091
468
P ANG015 Angioedema 54 0.091
469
THR016 Thrombophlebitis 51 0.091
470
HMG002 Hemoglobinuria 49 0.090
471
c CHR682 Chronic Bilirubin Encephalopathy 38 0.090
472
MNT001 Mantle Cell Lymphoma 66 0.090
473
c ACQ042 Acquired Hemophilia a 37 0.090
474
PLS009 Plasma Cell Neoplasm 51 0.090
475
THR013 Thoracic Outlet Syndrome 53 0.090
476
P CRN037 Craniosynostosis 68 0.089
477
ILS001 Ileus 51 0.089
478
GLM044 Glomerular Disease 39 0.089
479
P PRP029 Porphyria 62 0.089
480
P CLL015 Collagen Disease 42 0.088
481
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.088
482
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.088
483
CHR066 Chronic Fatigue Syndrome 61 0.088
484
P MYM013 Moyamoya Disease 1 54 0.088
485
HPR003 Heparin-Induced Thrombocytopenia 47 0.087
486
HMT002 Hematologic Cancer 62 0.087
487
ART004 Aortic Atherosclerosis 48 0.087
488
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.087
489
P TRC086 Trichohepatoenteric Syndrome 1 59 0.086
490
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.086
491
GRY002 Gray Platelet Syndrome 58 0.086
492
CRT004 Carotid Artery Thrombosis 38 0.086
493
HRY003 Hairy Cell Leukemia 55 0.085
494
P FBR031 Febrile Seizures 51 0.085
495
DVR002 Diverticulitis 44 0.085
496
CRY004 Cryoglobulinemia 49 0.085
497
CRB086 Cerebral Aneurysms 40 0.085
498
P AXN002 Axenfeld-Rieger Syndrome 58 0.085
499
P VNS003 Venous Insufficiency 55 0.085
500
c FNC043 Fanconi Anemia, Complementation Group E 62 0.085
501
c GRV008 Graves Disease 1 55 0.084
502
PRT011 Protein C Deficiency 45 0.084
503
MRG003 Marginal Zone B-Cell Lymphoma 53 0.084
504
BDD001 Budd-Chiari Syndrome 62 0.084
505
FNT004 Fainting 31 0.084
506
P EHL001 Ehlers-Danlos Syndrome 57 0.084
507
SRC027 Sarcoma, Synovial 56 0.084
508
GLS018 Glass Syndrome 53 0.083
509
END062 Endometrial Hyperplasia 48 0.083
510
P CPL006 Capillary Hemangioma 51 0.083
511
CRD223 Cardiac Arrhythmia 60 0.082
512
c FML035 Familial Hyperlipidemia 55 0.082
513
ACT064 Acute Necrotizing Encephalitis 32 0.082
514
MRF001 Marfan Syndrome 75 0.082
515
GNG012 Gingival Overgrowth 51 0.082
516
NSS002 Neisseria Meningitidis Infection 46 0.081
517
PRT058 Pure Autonomic Failure 59 0.081
518
ATX010 Ataxia Neuropathy Spectrum 38 0.081
519
P HST010 Histiocytosis 53 0.081
520
BLD137 Blood Group--Ahonen 19 0.081
521
LPD004 Lipoid Nephrosis 47 0.081
522
c PRG020 Paragangliomas 3 38 0.080
523
ALC006 Alcoholic Hepatitis 61 0.080
524
P INT070 Intestinal Obstruction 58 0.080
525
ANV001 Anovulation 47 0.080
526
P NNN008 Noonan Syndrome 1 76 0.080
527
P ALP009 Alopecia Areata 60 0.080
528
BRN032 Brain Glioma 43 0.080
529
INT078 Intracranial Thrombosis 48 0.079
530
URT010 Ureteral Obstruction 46 0.079
531
P CMP008 Compartment Syndrome 48 0.079
532
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.079
533
ART001 Arterial Tortuosity Syndrome 66 0.079
534
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.078
535
P ALP106 Alport Syndrome 1, X-Linked 55 0.078
536
FBR019 Fibromatosis 44 0.078
537
c HRD002 Hereditary Angioedema 61 0.078
538
c INF071 Inflammatory Bowel Disease 1 68 0.078
539
PRC013 Pericarditis 54 0.078
540
LYM012 Lymphoplasmacytic Lymphoma 61 0.078
541
VTM033 Vitamin K Deficiency Bleeding 48 0.077
542
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.077
543
P SJG008 Sjogren Syndrome 56 0.077
544
LYM021 Lymphadenitis 58 0.077
545
HYP081 Hypolipoproteinemia 50 0.077
546
ALR002 Al-Raqad Syndrome 34 0.077
547
P HMC002 Homocystinuria 54 0.076
548
P OVR049 Ovarian Disease 53 0.076
549
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.076
550
P ATR010 Atrial Heart Septal Defect 60 0.076
551
PLC005 Placental Insufficiency 57 0.076
552
NWB001 Newborn Respiratory Distress Syndrome 58 0.076
553
P HRM001 Hermansky-Pudlak Syndrome 65 0.076
554
WRN001 Werner Syndrome 69 0.076
555
MLD001 Melioidosis 67 0.075
556
SNS003 Sensory Peripheral Neuropathy 53 0.075
557
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.075
558
c BLD140 Blood Group, I System 30 0.075
559
P CCK001 Cockayne Syndrome 66 0.075
560
P PLY017 Polyarteritis Nodosa 58 0.075
561
P MGR001 Migraine Without Aura 48 0.075
562
P PLT029 Platelet Groups--Ko System 16 0.075
563
ATN004 Autonomic Neuropathy 44 0.075
564
P RNL015 Renal Hypertension 48 0.074
565
c CNG006 Congenital Hypothyroidism 65 0.074
566
WLL001 Williams-Beuren Syndrome 62 0.073
567
CCN002 Cocaine Abuse 48 0.073
568
c LPM012 Lipomatosis, Multiple 59 0.072
569
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.072
570
ISL003 Isolated Growth Hormone Deficiency 52 0.072
571
MRK001 Merkel Cell Carcinoma 66 0.072
572
PRS042 Prostate Disease 44 0.072
573
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.071
574
P AGG001 Aggressive Periodontitis 50 0.071
575
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.071
576
RDN001 Reading Disorder 40 0.070
577
HPT082 Hepatic Adenomas, Familial 37 0.070
578
PLM005 Pleomorphic Lipoma 39 0.070
580
c CHR431 Chronic Venous Insufficiency 49 0.069
581
NNT012 Neonatal Jaundice 53 0.069
582
c SYS004 Systemic Mastocytosis 63 0.069
583
CMP010 Complex Regional Pain Syndrome 58 0.069
584
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.069
585
P SYR001 Syringomyelia 46 0.069
586
SYR010 Syringomyelia, Noncommunicating Isolated 37 0.069
587
KRN001 Korean Hemorrhagic Fever 34 0.069
588
CMM004 Common Variable Immunodeficiency 67 0.069
589
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 45 0.069
590
CRD001 Cardiac Tamponade 46 0.069
591
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.069
592
RDC006 Red Cell Aplasia 42 0.069
593
c INH004 Inherited Blood Coagulation Disease 34 0.068
594
ADP007 Adie Pupil 39 0.068
595
HNM002 Hinman Syndrome 29 0.068
596
P PSD087 Pseudoxanthoma Elasticum 67 0.068
597
END072 Endotheliitis 35 0.067
598
ALB002 Albinism 46 0.067
599
c SYS043 Systemic Lupus Erythematosus 1 38 0.067
600
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.067
601
DGR001 Digeorge Syndrome 63 0.067
602
ADR005 Adrenal Carcinoma 58 0.067
603
AMB001 Amebiasis 49 0.067
604
P ACR001 Aicardi-Goutieres Syndrome 65 0.066
605
CRT015 Carotid Artery Occlusion 44 0.066
606
FBR012 Fabry Disease 71 0.066
607
MXD005 Mixed Connective Tissue Disease 59 0.066
608
SCR008 Scrub Typhus 58 0.065
609
P PRR002 Pure Red-Cell Aplasia 48 0.065
610
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.065
611
NRG002 Neurogenic Bladder 54 0.065
612
P MTR012 Mitral Valve Disease 57 0.065
613
SPL004 Splenic Marginal Zone Lymphoma 51 0.065
614
SYS003 Systolic Heart Failure 50 0.065
615
HYP114 Hypertensive Nephropathy 34 0.064
616
LNG108 Langerhans Cell Histiocytosis 58 0.064
617
CLC006 Calcinosis 48 0.064
618
NTR018 Neutrophilia, Hereditary 52 0.064
619
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.064
620
P FML018 Familial Mediterranean Fever 72 0.064
621
CRT016 Carotid Artery Disease 52 0.064
622
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.064
623
DNG001 Dengue Shock Syndrome 43 0.064
624
P PRG092 Pregnancy Loss, Recurrent 1 40 0.064
625
P CRC039 Coarctation of Aorta 47 0.064
626
OLG006 Oligoastrocytoma 35 0.063
627
PRC002 Paracoccidioidomycosis 53 0.063
628
IDP033 Idiopathic Edema 43 0.062
629
P PST095 Post-Thrombotic Syndrome 50 0.062
630
c ART115 Aortic Valve Disease 1 75 0.062
631
MTY003 Mutyh Polyposis 29 0.062
632
HMR039 Hemorrhage, Intracerebral 57 0.062
633
SYS071 Systemic Autoimmune Disease 37 0.062
634
c PSD047 Pseudo-Turner Syndrome 21 0.062
635
c BRC062 Brachydactyly, Type D 36 0.062
636
ANT009 Antithrombin Iii Deficiency 59 0.062
637
GYN001 Gynecomastia 49 0.061
638
FRN014 Fournier Gangrene 37 0.061
639
PTN001 Patent Foramen Ovale 56 0.061
640
INF021 Infant Gynecomastia 31 0.061
641
LYM008 Lymphangiosarcoma 44 0.061
642
HMP018 Hemophilic Arthropathy 34 0.061
643
c MLG069 Malignant Hypertension 47 0.061
644
P MLT007 Multiple Epiphyseal Dysplasia 58 0.061
645
MXD026 Mixed Glioma 45 0.060
646
P IGN003 Iga Nephropathy 1 49 0.060
647
ACT088 Acute Insulin Response 41 0.060
648
RTN001 Retinal Vasculitis 46 0.060
649
BTN002 Boutonneuse Fever 39 0.059
650
P PLY020 Polyradiculoneuropathy 46 0.059
651
GRN037 Granulomatosis with Polyangiitis 64 0.059
652
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 30 0.059
653
MST024 Mastocytosis, Cutaneous 67 0.059
654
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.058
655
ICH001 Ichthyosis Vulgaris 55 0.058
656
APH001 Aphthous Stomatitis 57 0.058
657
PRT012 Prothrombin Deficiency 41 0.058
658
ALC009 Alcoholic Liver Cirrhosis 53 0.058
659
P MGL001 Megaloblastic Anemia 55 0.058
660
HNC001 Henoch-Schoenlein Purpura 54 0.058
661
GRN034 Grange Syndrome 55 0.058
662
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.058
663
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 44 0.058
664
CRB132 Cerebral Sinovenous Thrombosis 33 0.057
665
MYC088 Mycobacterium Avium Complex Infections 29 0.057
666
APR006 Apert Syndrome 70 0.057
667
PPL001 Papillary Adenoma 45 0.057
668
ACR008 Acrocallosal Syndrome 68 0.057
669
PYG006 Pyogenic Granuloma 40 0.057
670
RCK002 Rocky Mountain Spotted Fever 40 0.056
671
P ESP035 Esophagitis, Eosinophilic, 1 54 0.055
672
P ERY008 Erythromelalgia 47 0.055
673
MCR088 Microscopic Polyangiitis 51 0.055
674
DBT008 Diabetic Angiopathy 44 0.055
675
PRN039 Paraneoplastic Syndromes 38 0.055
676
P TRC102 Trichothiodystrophy 1, Photosensitive 65 0.054
677
CHL028 Childhood Type Dermatomyositis 60 0.054
678
P RNL017 Renal Oncocytoma 53 0.054
679
SPL009 Splenic Sequestration 36 0.054
680
P HMN036 Hemangiopericytoma, Malignant 58 0.054
681
BLD163 Blood Group, Dombrock System 26 0.054
682
BLD165 Blood Group, Colton System 23 0.054
683
c HMG003 Hemoglobin E Disease 43 0.053
684
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.053
685
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.053
686
ASP030 Aspirin Resistance 40 0.053
687
VNW009 Von Willebrand Disease, X-Linked Form 7 0.053
688
TQP001 Taqi Polymorphism 32 0.053
689
ABT001 Abetalipoproteinemia 67 0.053
690
c INT064 Intermediate Uveitis 55 0.052
691
FLT011 Felty Syndrome 52 0.052
693
HYP063 Hypersplenism 53 0.052
694
P OCL002 Oculocutaneous Albinism 60 0.052
695
PRD004 Prediabetes Syndrome 47 0.052
696
GST020 Gastric Antral Vascular Ectasia 41 0.051
697
P PRP034 Purpura Fulminans 42 0.051
698
P PTT014 Pitt-Hopkins Syndrome 60 0.051
699
AND005 Androgen Insensitivity Syndrome, Mild 22 0.051
700
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.051
701
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.051
702
NDL024 Nodal Marginal Zone Lymphoma 39 0.051
703
BRN026 Branch Retinal Artery Occlusion 43 0.051
704
c PRM225 Primary Thrombocytopenia 41 0.051
705
c CNT075 Central Precocious Puberty 47 0.050
706
HRP009 Herpes Simplex Encephalitis 50 0.050
707
ANL018 Analbuminemia 54 0.050
708
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.050
709
ART006 Arthus Reaction 42 0.049
710
P CRN074 Coronary Artery Aneurysm 39 0.049
711
MTR087 Maternal Uniparental Disomy 30 0.049
712
c MLT142 Multiple Epiphyseal Dysplasia, Autosomal Dominant 24 0.049
713
RNL024 Renal Glucosuria 57 0.049
714
c CLR080 Colorectal Cancer 5 31 0.049
715
QBC001 Quebec Platelet Disorder 42 0.049
716
ICH002 Ichthyosis Bullosa of Siemens 44 0.049
717
CVR006 Cavernous Hemangioma 49 0.049
718
TKY002 Takayasu Arteritis 61 0.048
719
RRC033 Rare Coagulation Disorder 15 0.048
720
CRB009 Cerebritis 36 0.048
721
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.047
722
P BTH005 Bethlem Myopathy 1 60 0.047
723
CHR008 Choroiditis 44 0.047
724
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.046
725
P SHR029 Short Syndrome 57 0.046
726
ACT017 Acute Chest Syndrome 50 0.046
727
MRN001 Marantic Endocarditis 38 0.046
728
P RNG032 Ring Chromosome 42 0.046
729
WHM001 Whim Syndrome 59 0.046
730
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.045
731
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.045
732
CTS003 Coats Disease 52 0.045
733
LCH001 Leech Infestation 36 0.045
734
SBV001 Subvalvular Aortic Stenosis 32 0.044
735
ADL030 Adult-Onset Still's Disease 58 0.044
736
WLF001 Wolff-Parkinson-White Syndrome 65 0.044
737
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.044
738
BNM001 Bone Marrow Cancer 43 0.044
739
PLM180 Pulmonary Artery Disease 35 0.044
740
ART012 Aortitis 43 0.044
741
CHR635 Chromosome 5q Deletion Syndrome 51 0.044
742
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 45 0.043
743
c HRM005 Hermansky-Pudlak Syndrome 1 50 0.043
744
BMB001 Bombay Phenotype 31 0.043
745
FMR003 Femoral Neuropathy 31 0.042
746
P CLS054 Classic Ehlers-Danlos Syndrome 54 0.042
747
c CNG029 Congenital Mesoblastic Nephroma 40 0.042
748
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.042
749
MCN017 Meconium Ileus 52 0.042
750
VLC001 Velocardiofacial Syndrome 54 0.042
751
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.042
752
HYP008 Hypertensive Retinopathy 39 0.042
753
NRR002 Norrie Disease 63 0.042
754
PSD007 Pseudomyxoma Peritonei 53 0.041
755
UNV002 Univentricular Heart 28 0.041
756
TRG019 Trigonocephaly with Short Stature and Developmental Delay 34 0.041
757
c WLM011 Wilms Tumor 6 37 0.040
758
CHR286 Chronic Neutrophilic Leukemia 41 0.040
759
ART110 Arteritic Anterior Ischemic Optic Neuropathy 34 0.040
760
c ACT078 Acute Porphyria 49 0.040
761
NDL013 Nodular Regenerative Hyperplasia 47 0.040
762
ATY042 Atypical Chronic Myeloid Leukemia 49 0.040
763
SPL006 Splenic Infarction 37 0.040
764
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.040
765
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.040
766
PLY010 Polyclonal Hypergammaglobulinemia 39 0.040
767
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.039
768
PLL001 Pallister-Hall Syndrome 64 0.039
769
ATM061 Autoimmune Polyglandular Syndrome Type 3 29 0.039
770
RCK009 Rickettsial Disease 20 0.039
771
HPT009 Hepatopulmonary Syndrome 49 0.039
772
INT003 Intracranial Hypotension 33 0.038
773
WRN003 Wernicke Encephalopathy 47 0.038
774
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.038
775
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 32 0.038
776
TRC062 Tricuspid Atresia 52 0.038
777
EXR008 Exercise-Induced Malignant Hyperthermia 21 0.038
778
DST005 Diastrophic Dysplasia 59 0.038
779
P MXL015 Maxillary Sinusitis 37 0.038
780
LMR001 Lemierre's Syndrome 40 0.038
781
GLC011 Galactose Epimerase Deficiency 48 0.037
782
STR089 Storage Pool Platelet Disease 47 0.037
783
PRT130 Protein Z Deficiency 25 0.037
784
LVR002 Liver Angiosarcoma 43 0.037
785
PLS032 Plasmodium Falciparum Blood Infection Level 22 0.036
786
PLM041 Pulmonary Valve Stenosis 49 0.036
787
P SPR013 Spiradenoma 33 0.036
788
CNT046 Central Nervous System Vasculitis 42 0.036
789
PLM070 Pulmonic Stenosis 57 0.036
790
PLT016 Platelet Adenylate Cyclase Activity 16 0.035
791
P PLY147 Polydactyly, Postaxial, Type A1 56 0.035
792
EVN001 Evans' Syndrome 46 0.035
793
XLN228 X-Linked Recessive Disease 26 0.035
794
HPT081 Hepatic Infarction 33 0.034
795
c THR090 Thrombocythemia 1 49 0.034
796
c THR037 Thrombocytopenia 2 37 0.034
798
VLK001 Volkmann Contracture 32 0.034
799
ADH006 Adhesive Otitis Media 30 0.034
800
CMP089 Complement Component 6 Deficiency 39 0.034
801
ODN023 Odontochondrodysplasia 61 0.033
802
c HRM009 Hermansky-Pudlak Syndrome 6 44 0.033
803
c MLT031 Multiple Epiphyseal Dysplasia, Recessive 19 0.033
804
GNT031 Genitopatellar Syndrome 42 0.033
805
DRR016 Diarrhea 2, with Microvillus Atrophy 57 0.032
806
P ULL002 Ullrich Congenital Muscular Dystrophy 1 56 0.032
807
TRC118 Trichodentoosseous Syndrome 34 0.031
808
P ARC016 Auriculocondylar Syndrome 1 40 0.031
809
INF005 Infiltrating Lipoma 26 0.031
810
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 56 0.031
811
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.031
812
c PRM039 Primary Angiitis of the Central Nervous System 33 0.031
813
MLR020 Malaria, Mild 28 0.030
814
c DFN136 Deafness, Autosomal Dominant 9 42 0.030
815
CYS047 Cystic Fibrosis, Modifier of, 1 16 0.030
816
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 0.029
817
c CHR038 Chronic Maxillary Sinusitis 30 0.029
818
SPN438 Spondyloepimetaphyseal Dysplasia, X-Linked, with Hypomyelinating Leukodystrophy 34 0.028
819
c EPP017 Epiphyseal Dysplasia, Multiple, 1 46 0.028
820
HPT066 Hepatoportal Sclerosis 24 0.028
821
CPL005 Capillary Disease 38 0.027
822
c RNG007 Ring Chromosome 12 27 0.027
823
c XLN230 X-Linked Monogenic Disease 20 0.027
Content
Loading form....