Search results for Heparin

1644 hits were found for Heparin

# Family MCID Name MIFTS Score
1
HPR006 Heparin Cofactor Ii Deficiency 29 8.661
2
HPR003 Heparin-Induced Thrombocytopenia 49 7.917
3
P THR014 Thrombocytopenia 67 1.028
4
c THR092 Thrombophilia Due to Thrombin Defect 74 0.675
5
PLM033 Pulmonary Embolism 60 0.614
6
THR024 Thrombosis 58 0.582
7
INT007 Intermediate Coronary Syndrome 58 0.355
8
ISC004 Ischemia 62 0.316
9
c ACT075 Acute Myocardial Infarction 59 0.290
10
DSS009 Disseminated Intravascular Coagulation 58 0.289
11
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.277
12
P MYC007 Myocardial Infarction 74 0.274
13
P THR015 Thrombophilia 51 0.237
14
P KDN018 Kidney Disease 73 0.235
15
P CRN018 Coronary Artery Anomaly 67 0.215
16
P ANT006 Antiphospholipid Syndrome 56 0.214
17
ANG054 Angina Pectoris 66 0.209
18
END030 End Stage Renal Failure 60 0.205
19
ALL026 Allergic Hypersensitivity Disease 65 0.203
20
c PRC016 Pre-Eclampsia 63 0.198
21
THR016 Thrombophlebitis 50 0.196
22
P VSC007 Vascular Disease 65 0.194
23
CRB039 Cerebrovascular Disease 71 0.191
24
48X005 48,xyyy 37 0.191
25
STR067 Stroke, Ischemic 82 0.190
26
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.188
27
ART140 Arteries, Anomalies of 60 0.187
28
c ACT071 Acute Kidney Failure 60 0.183
29
ATH013 Atherosclerosis Susceptibility 68 0.179
30
RRD056 Rare Disease in Surgical Orthopedic 29 0.163
31
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.162
32
c CHR684 Chronic Kidney Disease 68 0.158
33
c ACT210 Acute Respiratory Distress Syndrome 59 0.158
34
P OST002 Osteoporosis 79 0.155
35
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.154
36
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.154
37
P ATR011 Atrial Fibrillation 67 0.152
38
P CRN300 Coronary Heart Disease 1 59 0.152
39
P GLM007 Glomerulonephritis 58 0.151
40
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.150
41
TXC005 Toxic Shock Syndrome 63 0.150
42
LMB062 Limb Ischemia 50 0.150
43
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.147
44
P ART021 Arteriosclerosis 56 0.147
45
PRP027 Peripheral Vascular Disease 72 0.144
46
P PLM037 Pulmonary Hypertension 69 0.143
47
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.143
48
CRN017 Coronary Thrombosis 45 0.140
49
ANT009 Antithrombin Iii Deficiency 57 0.139
50
P CRD119 Cardiac Arrest 71 0.134
51
PRP030 Purpura 56 0.134
52
PLC008 Placenta Disease 51 0.134
53
CRD137 Cardiogenic Shock 50 0.133
54
ART016 Aortic Aneurysm 71 0.132
55
LVR012 Liver Cirrhosis 67 0.132
56
CYT002 Cytokine Deficiency 46 0.132
57
P HYP750 Hypertriglyceridemia, Familial 62 0.131
58
MST004 Mast Cell Neoplasm 40 0.131
59
EXT007 Extracutaneous Mastocytoma 39 0.131
60
P ECL001 Eclampsia 53 0.128
61
CLT003 Colitis 63 0.127
62
P HRT032 Heart Disease 78 0.126
63
c ACT027 Acute Pancreatitis 60 0.126
64
ANR040 Aneurysm 60 0.125
65
ULC004 Ulcerative Colitis 75 0.122
66
c HYP836 Hypercholesterolemia, Familial, 1 74 0.121
67
PRT036 Peritonitis 66 0.121
68
SPN186 Spinal Cord Injury 63 0.121
69
P CLR023 Colorectal Cancer 100 0.120
70
P PNC044 Pancreatitis 61 0.120
71
P CTR002 Cataract 62 0.116
72
BNR002 Bone Resorption Disease 51 0.114
73
P PST095 Post-Thrombotic Syndrome 50 0.114
74
P OVR042 Ovarian Cancer 89 0.113
75
P RSP003 Respiratory Failure 75 0.113
76
P LVR013 Liver Disease 71 0.113
77
P NPH012 Nephrotic Syndrome 65 0.113
78
P END033 Endocarditis 58 0.113
79
c SYS001 Systemic Lupus Erythematosus 88 0.112
80
HRD083 Hereditary Antithrombin Deficiency 30 0.112
81
47X002 47,xyy 49 0.110
82
P INT143 Interstitial Cystitis 62 0.109
83
HLX001 Helix Syndrome 46 0.109
84
CNG034 Congestive Heart Failure 69 0.107
85
c RHB024 Rhabdomyosarcoma 2 64 0.107
86
DRM006 Dermatitis 63 0.107
87
P LPS004 Lupus Erythematosus 62 0.107
88
TRN015 Transient Cerebral Ischemia 62 0.107
89
P CYS018 Cystitis 59 0.107
90
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.107
91
P PNC035 Pancreatic Cancer 86 0.106
92
P INF032 Infertility 60 0.106
93
HPT046 Hepatic Veno-Occlusive Disease 56 0.106
94
c SVR005 Severe Pre-Eclampsia 50 0.106
95
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.104
96
PLM010 Pulmonary Edema 56 0.104
97
VTM033 Vitamin K Deficiency Bleeding 47 0.104
98
RRS014 Rare Surgical Neurologic Disease 33 0.104
99
PNG002 Pain Agnosia 52 0.103
100
P NTR004 Neutropenia 64 0.101
101
ATM095 Autoimmune Disease 62 0.101
102
THR004 Thrombocytosis 52 0.100
103
P BRS047 Breast Cancer 99 0.098
104
c MCR113 Microvascular Complications of Diabetes 3 55 0.098
105
PRT018 Portal Vein Thrombosis 50 0.098
106
c MCR120 Microvascular Complications of Diabetes 7 48 0.098
107
c MCR130 Microvascular Complications of Diabetes 6 42 0.098
108
c MCR133 Microvascular Complications of Diabetes 4 42 0.098
109
P VSC011 Vasculitis 64 0.097
110
DFC004 Deficiency Anemia 77 0.095
111
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.095
112
DPH001 Diphtheria 61 0.095
113
PLC007 Placental Abruption 47 0.095
114
P PRG092 Pregnancy Loss, Recurrent 1 40 0.095
115
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.093
116
VRC005 Varicose Veins 61 0.092
117
ATX019 Ataxia with Vitamin E Deficiency 46 0.092
118
P LNG032 Lung Cancer 99 0.090
119
P AMY004 Amyloidosis 71 0.090
120
P INF037 Inflammatory Bowel Disease 57 0.090
121
P LYM031 Lymphocytic Leukemia 56 0.090
122
c FML001 Familial Atrial Fibrillation 67 0.088
123
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.088
124
P URT039 Urticaria 61 0.088
125
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.086
126
P TRN020 Turner Syndrome 66 0.086
127
P ADN016 Adenocarcinoma 65 0.086
128
P HML002 Hemolytic Anemia 64 0.086
129
ADL002 Adult Syndrome 62 0.086
130
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.086
131
PRN019 Perinatal Necrotizing Enterocolitis 55 0.086
132
TRM010 Traumatic Brain Injury 54 0.086
133
ENT011 Enterocolitis 51 0.086
134
VTR007 Vitreoretinopathy 48 0.086
135
c HYP595 Hypertension, Essential 87 0.085
136
DWN001 Down Syndrome 70 0.085
137
P DBT009 Diabetes Mellitus 66 0.085
138
P NRB010 Neuroblastoma 1 66 0.085
139
P GLM045 Glioma 64 0.085
140
BCT022 Bacterial Infectious Disease 57 0.085
141
PRT011 Protein C Deficiency 45 0.085
142
P HPT023 Hepatocellular Carcinoma 99 0.083
143
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.083
144
P MCR115 Microvascular Complications of Diabetes 5 67 0.083
145
NTR005 Nutritional Deficiency Disease 61 0.083
146
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.083
147
BRN071 Brain Injury 51 0.083
148
MYL069 Myeloma, Multiple 85 0.081
149
P ESS003 Essential Thrombocythemia 69 0.081
150
P LKM062 Leukemia, Acute Lymphoblastic 68 0.081
151
P HRP006 Herpes Simplex 66 0.081
152
P ADL010 Adult Respiratory Distress Syndrome 61 0.081
153
GLL048 Glial Tumor 48 0.081
154
c PRM038 Primary Agammaglobulinemia 45 0.081
155
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.081
156
P GST053 Gastric Cancer 85 0.079
157
GLB002 Glioblastoma 74 0.079
158
P PNM007 Pneumonia 71 0.079
159
MLN008 Melanoma 68 0.079
160
P HYP098 Hypereosinophilic Syndrome 67 0.079
161
P PSR002 Psoriasis 63 0.079
162
RTN017 Retinal Detachment 62 0.079
163
GLB015 Glioblastoma Multiforme 60 0.079
164
INT002 Intermittent Claudication 60 0.079
165
P UVT001 Uveitis 58 0.079
166
P NRP001 Neuropathy 57 0.079
167
PRP016 Paraplegia 54 0.079
168
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.079
169
PST011 Pustulosis of Palm and Sole 51 0.079
170
VCC001 Vaccinia 50 0.079
171
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.079
172
PRT014 Protein S Deficiency 50 0.079
173
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.079
174
MTB004 Metabolic Acidosis 48 0.079
175
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.079
176
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.079
177
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.079
178
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.079
179
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.079
180
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.079
181
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.079
183
P EXN002 Exanthem 58 0.077
184
P VNS003 Venous Insufficiency 55 0.077
185
P CMP008 Compartment Syndrome 45 0.077
186
P BCT020 Bacteremia 2 45 0.077
187
PLT015 Platelet Aggregation, Spontaneous 40 0.077
188
P PRS040 Prostate Cancer 97 0.075
189
HMN044 Human Immunodeficiency Virus Type 1 73 0.075
190
P MNN013 Meningitis 67 0.075
191
IDP011 Idiopathic Interstitial Pneumonia 65 0.075
192
CLN015 Colon Adenocarcinoma 65 0.075
193
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.075
194
ACT119 Acute Promyelocytic Leukemia 63 0.075
195
LNG099 Lung Disease 62 0.075
196
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.075
197
OCL069 Ocular Motor Apraxia 53 0.075
198
HDN002 Head Injury 47 0.075
199
PRP007 Priapism 47 0.075
200
P HYP120 Hypoaldosteronism 38 0.075
201
P BLD134 Bladder Cancer 79 0.073
202
P LKM002 Leukemia 69 0.073
203
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.073
204
P PLM036 Pulmonary Fibrosis 66 0.073
205
HYP066 Hyperglycemia 63 0.073
206
P HMP007 Hemophilia 58 0.073
207
P SCK005 Sickle Cell Disease 53 0.073
208
HRT011 Heart Septal Defect 52 0.073
209
PRP080 Peripheral Artery Disease 51 0.073
210
HYP189 Hypoadrenalism 39 0.073
211
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.073
212
CYS001 Cystic Fibrosis 84 0.071
213
AST005 Asthma 80 0.071
214
OST012 Osteoarthritis 80 0.071
215
c FML021 Familial Hypercholesterolemia 67 0.071
216
BDD001 Budd-Chiari Syndrome 62 0.071
217
SQM006 Squamous Cell Carcinoma 60 0.071
218
P PLY018 Polycythemia 56 0.071
219
PLC005 Placental Insufficiency 55 0.071
220
P HML001 Hemolytic-Uremic Syndrome 54 0.071
221
P MTR003 Mitral Valve Stenosis 54 0.071
222
P PRP034 Purpura Fulminans 42 0.071
223
CRB086 Cerebral Aneurysms 41 0.071
224
LPT014 Leptin Deficiency or Dysfunction 72 0.068
225
c SML038 Small Cell Cancer of the Lung 67 0.068
226
OST159 Osteogenic Sarcoma 67 0.068
227
LPD008 Lipid Metabolism Disorder 64 0.068
228
c ACT068 Acute Cystitis 63 0.068
229
PRT013 Portal Hypertension 61 0.068
230
P BRS044 Breast Adenocarcinoma 59 0.068
231
RHM027 Rheumatic Disease 56 0.068
232
HMT018 Hematopoietic Stem Cell Transplantation 54 0.068
233
URM002 Uremia 50 0.068
234
CRB004 Cerebral Artery Occlusion 38 0.068
235
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.066
236
MLR004 Malaria 82 0.066
237
PLM001 Pulmonary Tuberculosis 72 0.066
238
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.066
239
P MST009 Mastocytosis 62 0.066
240
INT030 Intracranial Aneurysm 57 0.066
241
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.066
242
FCT001 Factor Viii Deficiency 54 0.066
243
HMG002 Hemoglobinuria 49 0.066
244
INT078 Intracranial Thrombosis 48 0.066
245
c HNT004 Huntington Disease-Like 2 48 0.066
246
INT010 Intracranial Embolism 47 0.066
247
STN005 St Anthony's Fire 18 0.066
248
P ALZ034 Alzheimer Disease 90 0.064
249
P RHM011 Rheumatoid Arthritis 82 0.064
250
IMM167 Immune Deficiency Disease 79 0.064
251
BRN024 Bronchitis 70 0.064
252
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.064
253
P MYL006 Myeloid Leukemia 61 0.064
254
P ATR010 Atrial Heart Septal Defect 61 0.064
255
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.064
256
P LCH002 Lichen Planus 55 0.064
257
c ACT134 Acute Liver Failure 53 0.064
258
CRN027 Corneal Neovascularization 48 0.064
259
XNT003 Xanthomatosis 48 0.064
260
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.064
261
c HNT011 Huntington Disease-Like 3 37 0.064
262
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.064
263
c LKM061 Leukemia, Acute Myeloid 84 0.061
264
INS024 Insulin-Like Growth Factor I 79 0.061
265
PLY001 Polycythemia Vera 70 0.061
266
SRC014 Sarcoma 67 0.061
267
c HPT016 Hepatitis B 63 0.061
268
P HMN010 Hemangioma 62 0.061
269
P MYC008 Myocarditis 60 0.061
270
P FBR017 Fibrosarcoma 57 0.061
271
SPN035 Spindle Cell Sarcoma 57 0.061
272
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.061
273
P HMR003 Hemorrhagic Disease 54 0.061
274
HLL004 Hellp Syndrome 53 0.061
275
GST023 Gastric Ulcer 53 0.061
276
STM007 Stomatitis 51 0.061
277
c CHR431 Chronic Venous Insufficiency 48 0.061
278
CRD001 Cardiac Tamponade 45 0.061
279
PRT019 Protein-Losing Enteropathy 41 0.061
280
LYM005 Lymphocele 35 0.061
281
SHW001 Shwartzman Phenomenon 35 0.061
282
PRT037 Pertussis 66 0.059
283
SKN016 Skin Disease 64 0.059
284
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.059
285
IRN002 Iron Metabolism Disease 58 0.059
286
HYP060 Hyperinsulinism 55 0.059
287
ACT058 Active Peptic Ulcer Disease 55 0.059
288
PRS045 Prostatic Hypertrophy 55 0.059
289
c GLL024 Gallbladder Disease 1 53 0.059
290
c MTR002 Mitral Valve Insufficiency 49 0.059
291
BWN001 Bowen-Conradi Syndrome 49 0.059
292
P BLD051 Blood Coagulation Disease 48 0.059
293
LYM019 Lymphosarcoma 48 0.059
294
BCK006 Back Pain 44 0.059
295
ANX004 Anoxia 44 0.059
296
THR123 Thrombotic Microangiopathy 41 0.059
297
c THR037 Thrombocytopenia 2 36 0.059
298
FMR003 Femoral Neuropathy 36 0.059
299
c ACQ005 Acquired Thrombocytopenia 34 0.059
300
SGT001 Sagittal Sinus Thrombosis 33 0.059
301
c LKM071 Leukemia, Chronic Lymphocytic 81 0.056
302
P LNG064 Lung Cancer Susceptibility 3 79 0.056
303
SVR004 Severe Combined Immunodeficiency 74 0.056
304
P PHC003 Pheochromocytoma 71 0.056
305
P HYP086 Hypothyroidism 70 0.056
306
P HPT021 Hepatitis 69 0.056
307
PNC129 Pancreatic Adenocarcinoma 69 0.056
308
HYP056 Hypoglycemia 68 0.056
309
c MCR129 Microvascular Complications of Diabetes 1 67 0.056
310
P OCL013 Oculodentodigital Dysplasia 65 0.056
311
c BRN108 Branchiootic Syndrome 1 62 0.056
312
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.056
313
c PNS012 Paine Syndrome 61 0.056
314
ACQ007 Acquired Immunodeficiency Syndrome 61 0.056
315
P HDC001 Headache 59 0.056
316
P ALP008 Alopecia 58 0.056
317
CNT047 Contact Dermatitis 58 0.056
318
AGN016 Aging 58 0.056
319
P PYL005 Pyelonephritis 58 0.056
320
HRT012 Heart Valve Disease 56 0.056
321
P RCT021 Rectum Cancer 54 0.056
322
P ANG015 Angioedema 54 0.056
323
CHR100 Chronic Ulcer of Skin 53 0.056
324
c LRG017 Large Intestine Cancer 53 0.056
325
ADR040 Adrenal Gland Pheochromocytoma 51 0.056
326
PRS129 Prostatic Hyperplasia, Benign 49 0.056
327
c MLG068 Malignant Glioma 46 0.056
328
c ACT150 Acute Adrenal Insufficiency 46 0.056
329
c MCR112 Microvascular Complications of Diabetes 2 42 0.056
330
c SBC003 Subacute Bacterial Endocarditis 33 0.056
332
c DLT002 Dilated Cardiomyopathy 81 0.053
333
CNN005 Connective Tissue Disease 68 0.053
334
MYL031 Myeloproliferative Neoplasm 66 0.053
335
OST017 Osteomyelitis 65 0.053
336
P ENC018 Encephalopathy 64 0.053
337
P ART005 Arteriovenous Malformation 63 0.053
338
P RHB003 Rhabdomyosarcoma 62 0.053
339
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.053
340
ING001 Inguinal Hernia 61 0.053
341
P BRN019 Bernard-Soulier Syndrome 60 0.053
342
c ACT073 Acute Leukemia 59 0.053
343
c HRD002 Hereditary Angioedema 59 0.053
344
CHL014 Cholera 58 0.053
345
P GST044 Gastritis 58 0.053
346
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.053
347
ENH001 Enhanced S-Cone Syndrome 56 0.053
348
RHM001 Rheumatic Fever 56 0.053
349
LNG031 Lung Benign Neoplasm 52 0.053
350
PRS021 Prostatic Adenoma 52 0.053
351
P RTN022 Retinal Vein Occlusion 50 0.053
352
c HYP768 Hyperlipoproteinemia, Type I 50 0.053
353
CLC001 Calciphylaxis 49 0.053
354
HMR002 Hemarthrosis 46 0.053
355
CYN002 Cyanosis, Transient Neonatal 45 0.053
356
ORL015 Oral Squamous Cell Carcinoma 44 0.053
357
HMP001 Hemopericardium 44 0.053
358
c LKM004 Leukemia, B-Cell, Chronic 35 0.053
359
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.053
360
ESP021 Esophageal Cancer 90 0.050
361
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.050
362
END057 Endometrial Cancer 74 0.050
363
SCK003 Sickle Cell Anemia 74 0.050
364
c HPT073 Hepatitis C Virus 74 0.050
365
P SRC025 Sarcoidosis 1 72 0.050
366
P ART022 Arthritis 71 0.050
367
c MGR028 Migraine with or Without Aura 1 70 0.050
368
P LYM118 Lymphoma 70 0.050
369
ALC007 Alcohol Dependence 68 0.050
370
BRK010 Burkitt Lymphoma 68 0.050
371
c ART101 Aortic Valve Disease 2 67 0.050
372
c HMP004 Hemophilia B 66 0.050
373
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.050
374
c FNC043 Fanconi Anemia, Complementation Group E 64 0.050
375
P ENC004 Encephalitis 64 0.050
376
CRC021 Carcinosarcoma 62 0.050
377
P BCL017 B-Cell Lymphoma 61 0.050
378
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.050
379
P VNT002 Ventricular Septal Defect 61 0.050
380
HYP266 Hypoxia 58 0.050
381
PTN001 Patent Foramen Ovale 57 0.050
382
SFT003 Soft Tissue Sarcoma 57 0.050
383
PNM008 Pneumothorax 56 0.050
384
c VRL010 Viral Hepatitis 56 0.050
385
MCS002 Mucositis 56 0.050
386
P PMP001 Pemphigus 56 0.050
387
GRN034 Grange Syndrome 55 0.050
388
AMN003 Amnestic Disorder 55 0.050
389
P HYP076 Hyperthyroidism 55 0.050
390
INF034 Infective Endocarditis 53 0.050
391
RYN005 Raynaud Phenomenon 50 0.050
392
CRN030 Coronary Stenosis 49 0.050
393
LPD004 Lipoid Nephrosis 48 0.050
394
ENT004 Enthesopathy 46 0.050
395
TRT001 Teratocarcinoma 44 0.050
396
DRG024 Drug Allergy 43 0.050
397
P PRL003 Proliferative Glomerulonephritis 43 0.050
398
P PRC031 Preeclampsia/eclampsia 1 42 0.050
399
DBT008 Diabetic Angiopathy 42 0.050
400
THR035 Thrombasthenia 42 0.050
401
CHR466 Chronic Thromboembolic Pulmonary Hypertension 41 0.050
402
MNN021 Meningococcemia 38 0.050
403
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 38 0.050
404
c MYC058 Myocardial Infarction 2 30 0.050
405
ARG004 Argyria 28 0.050
406
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.047
407
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.047
408
c ATR087 Atrial Standstill 1 76 0.047
409
c LKM063 Leukemia, Chronic Myeloid 74 0.047
410
P CNR004 Cone-Rod Dystrophy 2 72 0.047
411
P CNJ013 Conjunctivitis 67 0.047
412
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.047
413
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.047
414
MST024 Mastocytosis, Cutaneous 65 0.047
415
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.047
416
BND020 Bone Disease 60 0.047
417
SPN027 Spinal Stenosis 58 0.047
418
TRN018 Transitional Cell Carcinoma 57 0.047
419
BRN004 Brain Edema 57 0.047
420
c FML035 Familial Hyperlipidemia 56 0.047
421
HMP005 Hemiplegia 55 0.047
422
MRG003 Marginal Zone B-Cell Lymphoma 55 0.047
423
HMC014 Homocysteinemia 54 0.047
424
OLG003 Oligohydramnios 53 0.047
425
GSG001 Gas Gangrene 52 0.047
426
OVR082 Overgrowth Syndrome 51 0.047
427
P PRC012 Pericardial Effusion 51 0.047
428
BLD053 Blood Platelet Disease 51 0.047
429
CRT013 Carotid Stenosis 50 0.047
430
P OVR046 Ovarian Cyst 50 0.047
431
IGG001 Iga Glomerulonephritis 50 0.047
432
c MLG074 Malignant Mesenchymoma 50 0.047
433
ESP002 Esophageal Varix 49 0.047
434
P AFB001 Afibrinogenemia 49 0.047
435
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.047
436
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.047
437
CLC006 Calcinosis 48 0.047
438
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.047
439
BHR001 Behr Syndrome 47 0.047
440
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.047
441
SYN036 Syncope 46 0.047
442
PRL017 Prolymphocytic Leukemia 45 0.047
443
P GLM044 Glomerular Disease 42 0.047
444
BRN026 Branch Retinal Artery Occlusion 41 0.047
445
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.047
446
ART008 Arteriosclerosis Obliterans 40 0.047
447
MRN001 Marantic Endocarditis 40 0.047
448
CRT004 Carotid Artery Thrombosis 37 0.047
449
PRT012 Prothrombin Deficiency 37 0.047
450
P ANT001 Anterolateral Myocardial Infarction 37 0.047
451
CRT008 Carotid Artery Dissection 36 0.047
452
c CHR682 Chronic Bilirubin Encephalopathy 36 0.047
454
SNG003 Single Ventricular Heart 31 0.047
455
P APL001 Aplastic Anemia 76 0.043
456
BRN028 Brain Cancer 75 0.043
457
LYM133 Lymphoma, Hodgkin, Classic 70 0.043
458
c HMP029 Hemophilia a 69 0.043
459
MYL005 Myelofibrosis 69 0.043
460
P GLM040 Glioma Susceptibility 1 68 0.043
461
P NSP012 Nasopharyngeal Carcinoma 67 0.043
462
P PRD008 Periodontitis 66 0.043
463
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.043
464
MSC007 Muscle Hypertrophy 65 0.043
465
KWS002 Kawasaki Disease 65 0.043
466
DPR016 Depression 64 0.043
467
P VNW001 Von Willebrand's Disease 64 0.043
468
HMT002 Hematologic Cancer 64 0.043
469
LSH001 Leishmaniasis 64 0.043
470
P THL005 Thalassemia 62 0.043
471
c AFB002 Afibrinogenemia, Congenital 62 0.043
472
TTN003 Tetanus 62 0.043
473
CHL068 Cholestasis 61 0.043
474
CHL123 Chlamydia 60 0.043
475
PPT005 Peptic Ulcer Disease 60 0.043
476
HMR039 Hemorrhage, Intracerebral 59 0.043
477
NWB001 Newborn Respiratory Distress Syndrome 58 0.043
478
P ALC033 Alcohol Use Disorder 58 0.043
479
LYM027 Lymphopenia 58 0.043
480
P DNG005 Dengue Virus 57 0.043
481
EMB004 Embryonal Carcinoma 57 0.043
482
VSC002 Vascular Dementia 57 0.043
483
PMP006 Pemphigus Vulgaris, Familial 56 0.043
484
ALL006 Allergic Asthma 56 0.043
485
HNC001 Henoch-Schoenlein Purpura 56 0.043
486
HYP005 Hypokalemia 55 0.043
487
SPT004 Septic Arthritis 55 0.043
488
P MMB011 Membranous Nephropathy 54 0.043
489
PLS007 Plasmodium Falciparum Malaria 53 0.043
490
P UTR058 Uterine Anomalies 53 0.043
491
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.043
492
HYP081 Hypolipoproteinemia 51 0.043
493
BLD044 Bladder Disease 50 0.043
494
c INF145 Infantile Liver Failure Syndrome 1 50 0.043
495
SPL004 Splenic Marginal Zone Lymphoma 48 0.043
496
ACT017 Acute Chest Syndrome 47 0.043
497
MNN020 Meningococcal Infection 46 0.043
498
ERY004 Erysipelas 46 0.043
499
P RTN014 Retinal Artery Occlusion 46 0.043
500
BCT021 Bacterial Sepsis 44 0.043
501
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.043
502
P KLZ004 Kala-Azar 1 43 0.043
503
GST020 Gastric Antral Vascular Ectasia 42 0.043
504
c HMG029 Hemoglobin Se Disease 40 0.043
505
SPR126 Superior Semicircular Canal Dehiscence 39 0.043
506
LGN005 Ligneous Conjunctivitis 36 0.043
507
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.043
508
CHL079 Children's Interstitial Lung Disease 27 0.043
509
URN022 Urinary Tract Infections, Recurrent 26 0.043
510
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.043
511
HYP736 Hyperheparinemia 12 0.043
512
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.039
513
CRV035 Cervical Cancer 77 0.039
514
CRH001 Crohn's Disease 75 0.039
515
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.039
516
OTT002 Otitis Media 71 0.039
517
P GRF003 Graft-Versus-Host Disease 71 0.039
518
P TTR001 Tetralogy of Fallot 70 0.039
519
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.039
520
MNT001 Mantle Cell Lymphoma 69 0.039
521
KRT019 Keratitis, Hereditary 69 0.039
522
P SYS005 Systemic Scleroderma 68 0.039
523
P MYS003 Myasthenia Gravis 68 0.039
524
P DMN002 Dementia 68 0.039
525
P MSC005 Muscular Dystrophy 68 0.039
526
P FLL037 Follicular Lymphoma 67 0.039
527
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.039
528
c DPH024 Diaphragmatic Hernia, Congenital 66 0.039
529
MGK001 Megakaryocytic Leukemia 65 0.039
530
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.039
531
P HYP069 Hyperparathyroidism 64 0.039
532
GT001 Gout 63 0.039
533
P LMY004 Leiomyosarcoma 63 0.039
534
FTT001 Fatty Liver Disease 63 0.039
535
P HYP055 Hypoplastic Left Heart Syndrome 63 0.039
536
P SNS001 Sensorineural Hearing Loss 62 0.039
537
c HPT001 Hepatitis C 62 0.039
538
c SCL052 Scleroderma, Familial Progressive 62 0.039
539
P ANP001 Anaplastic Large Cell Lymphoma 62 0.039
540
P KDN017 Kidney Cancer 60 0.039
541
ADN018 Adenoma 60 0.039
542
P SZR006 Seizure Disorder 59 0.039
543
P SYP003 Syphilis 59 0.039
544
URN010 Urinary Tract Obstruction 59 0.039
545
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.039
546
P PLY011 Polycystic Ovary Syndrome 58 0.039
547
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.039
548
PLS011 Plasmacytoma 57 0.039
549
GST050 Gastrointestinal System Disease 57 0.039
550
P PRN023 Prion Disease 57 0.039
551
HMG005 Hemoglobinopathy 57 0.039
552
CLL003 Cellulitis 56 0.039
553
CRH005 Crohn's Colitis 56 0.039
554
c BCT007 Bacterial Meningitis 56 0.039
555
P DRR001 Diarrhea 55 0.039
556
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.039
557
INT075 Intracranial Hypertension 54 0.039
558
PRC013 Pericarditis 54 0.039
559
LYM040 Lymphoblastic Lymphoma 54 0.039
560
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.039
561
CHC001 Chickenpox 53 0.039
562
P RTN018 Retinal Disease 53 0.039
563
CRT016 Carotid Artery Disease 53 0.039
564
P CNT005 Central Nervous System Lymphoma 52 0.039
565
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
566
c XNT010 Xanthinuria, Type I 51 0.039
567
GLS018 Glass Syndrome 51 0.039
568
HYP063 Hypersplenism 51 0.039
569
P DDN001 Duodenal Ulcer 50 0.039
570
c FLL041 Follicular Lymphoma 1 50 0.039
571
c PRM226 Primary Central Nervous System Lymphoma 50 0.039
572
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.039
573
RTN020 Retinal Vascular Disease 49 0.039
574
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.039
575
c CNT016 Central Retinal Vein Occlusion 48 0.039
576
P TCL004 T-Cell Leukemia 48 0.039
577
PLS025 Plasmablastic Lymphoma 48 0.039
578
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.039
579
RTC005 Reticulosarcoma 48 0.039
580
c PRM093 Premature Ovarian Failure 7 48 0.039
581
P HMR005 Hemorrhoid 47 0.039
582
NSS002 Neisseria Meningitidis Infection 47 0.039
583
PRP009 Peripartum Cardiomyopathy 47 0.039
584
LPT006 Leptin Receptor Deficiency 47 0.039
585
P RPD001 Rapidly Progressive Glomerulonephritis 46 0.039
586
HMP009 Haemophilus Influenzae 46 0.039
587
P HRN001 Horner's Syndrome 46 0.039
588
INT276 Interatrial Communication 46 0.039
589
PNM013 Pneumococcal Meningitis 45 0.039
590
c PCH010 Pachyonychia Congenita 3 43 0.039
591
ASP030 Aspirin Resistance 42 0.039
592
RDN001 Reading Disorder 42 0.039
593
c CNT028 Central Retinal Artery Occlusion 40 0.039
594
P INT260 Intracranial Berry Aneurysm 38 0.039
595
SCR011 Scrapie 37 0.039
596
MXD026 Mixed Glioma 36 0.039
597
c LKM005 Leukemia, T-Cell, Chronic 35 0.039
598
DSS010 Dissociative Disorder 35 0.039
600
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.039
601
TRN012 Transient Global Amnesia 34 0.039
602
c PRS136 Prostate Cancer, Hereditary, 6 34 0.039
603
c PRS130 Prostate Cancer, Hereditary, 8 33 0.039
604
GNT005 Giant Hemangioma 31 0.039
605
RSP007 Respiratory Distress Syndrome, Infant 31 0.039
606
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.039
607
c THR102 Thrombocytopenia 5 28 0.039
608
INT076 Intracranial Sinus Thrombosis 22 0.039
609
P ATX030 Ataxia-Telangiectasia 83 0.035
610
P PRK057 Parkinson Disease, Late-Onset 77 0.035
611
KPS004 Kaposi Sarcoma 75 0.035
612
c MNN043 Meningioma, Familial 74 0.035
613
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.035
614
c BTT014 Beta-Thalassemia 73 0.035
615
MYL009 Myelodysplastic Syndrome 72 0.035
616
P MYC084 Mycobacterium Tuberculosis 1 69 0.035
617
P HYD006 Hydrocephalus 68 0.035
618
CRT072 Creutzfeldt-Jakob Disease 67 0.035
619
MSM014 Mismatch Repair Cancer Syndrome 65 0.035
620
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 65 0.035
621
P PRP019 Peripheral Nervous System Disease 64 0.035
622
ANR007 Anorexia Nervosa 64 0.035
623
KRN002 Kearns-Sayre Syndrome 64 0.035
624
MNN042 Meningioma, Radiation-Induced 64 0.035
625
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.035
626
OVR029 Ovarian Hyperstimulation Syndrome 63 0.035
627
c WLM018 Wilms Tumor 5 63 0.035
628
c SYS004 Systemic Mastocytosis 63 0.035
629
P FCL005 Focal Segmental Glomerulosclerosis 63 0.035
630
VRL011 Viral Infectious Disease 62 0.035
631
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.035
632
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.035
633
P TXP001 Toxoplasmosis 61 0.035
634
CHL067 Cholecystitis 60 0.035
635
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.035
636
P PTN014 Patent Ductus Arteriosus 1 60 0.035
637
MNT002 Mental Depression 60 0.035
638
ART141 Arteriovenous Malformations of the Brain 60 0.035
639
c MCL013 Mucolipidosis Iv 60 0.035
640
P INT070 Intestinal Obstruction 60 0.035
641
EYD002 Eye Disease 59 0.035
642
VSL002 Visual Epilepsy 58 0.035
643
P HYP726 Hypercalcemia, Infantile, 1 58 0.035
644
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.035
645
YLL002 Yellow Fever 58 0.035
646
BLR008 Bilirubin Metabolic Disorder 58 0.035
647
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.035
648
FCT003 Factor X Deficiency 57 0.035
649
P CHN012 Chondrosarcoma 57 0.035
650
c ANG068 Angioedema, Hereditary, Type I 57 0.035
651
PRS047 Prostatitis 57 0.035
652
EXF001 Exfoliation Syndrome 56 0.035
653
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.035
654
ATR057 Atrioventricular Block 56 0.035
655
c SVR001 Severe Acute Respiratory Syndrome 56 0.035
656
JPN002 Japanese Encephalitis 56 0.035
657
PPL022 Papilloma 56 0.035
658
c CNG216 Congenital Hydrocephalus 55 0.035
659
P PLM034 Pulmonary Emphysema 55 0.035
660
MSS001 Masa Syndrome 55 0.035
661
GLC003 Glucose Intolerance 55 0.035
662
VSC003 Visceral Leishmaniasis 55 0.035
663
P SML001 Small Cell Carcinoma 55 0.035
664
PRM042 Primary Effusion Lymphoma 55 0.035
665
CLR030 Clear Cell Renal Cell Carcinoma 54 0.035
666
NTR018 Neutrophilia, Hereditary 53 0.035
667
IMP005 Impotence 53 0.035
668
HMT008 Hematuria, Benign Familial 53 0.035
669
DYS073 Dysphagia 52 0.035
670
LMY002 Leiomyoma 52 0.035
671
CLN045 Colonic Benign Neoplasm 52 0.035
672
c INH020 Inherited Metabolic Disorder 51 0.035
673
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 51 0.035
674
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.035
675
MNC006 Monoclonal Gammopathy of Uncertain Significance 50 0.035
676
ACR041 Acromelic Frontonasal Dysostosis 50 0.035
677
c THR071 Thrombocytopenia 1 50 0.035
678
ECT026 Ectopic Pregnancy 50 0.035
679
PRS030 Persistent Fetal Circulation Syndrome 50 0.035
680
MCR004 Macroglobulinemia 50 0.035
681
P CLB034 Coloboma, Ocular, Autosomal Dominant 50 0.035
682
P DRM007 Dermatitis Herpetiformis 50 0.035
683
GST049 Gastrointestinal System Cancer 49 0.035
684
FML026 Familial Lipoprotein Lipase Deficiency 49 0.035
685
NTR046 Neutrophil Migration 49 0.035
686
SQM002 Squamous Cell Papilloma 49 0.035
687
c PRG126 Progressive Familial Heart Block 49 0.035
688
HYP043 Hyperandrogenism 48 0.035
689
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.035
690
BNM001 Bone Marrow Cancer 48 0.035
691
RGH001 Right Bundle Branch Block 48 0.035
692
c THR090 Thrombocythemia 1 47 0.035
693
CHR074 Choriocarcinoma 47 0.035
694
PNN001 Panniculitis 47 0.035
695
LFT001 Left Bundle Branch Hemiblock 47 0.035
696
FSC004 Fasciitis 47 0.035
697
P RNL015 Renal Hypertension 47 0.035
698
ANR004 Anuria 47 0.035
699
c MLG069 Malignant Hypertension 46 0.035
700
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.035
701
KRT013 Keratolytic Winter Erythema 45 0.035
702
ART031 Aortic Coarctation 45 0.035
703
SMT001 Somatization Disorder 45 0.035
704
c ACT076 Acute Myocarditis 45 0.035
705
ANG011 Angiodysplasia 45 0.035
706
c CLR017 Clear Cell Sarcoma 45 0.035
707
PTT004 Pituitary Apoplexy 44 0.035
708
SDD008 Sudden Sensorineural Hearing Loss 44 0.035
709
PLR007 Pleural Empyema 44 0.035
710
CRT015 Carotid Artery Occlusion 44 0.035
711
HYP457 Hypertrophic Scars 44 0.035
712
c CHR064 Chronic Monocytic Leukemia 43 0.035
713
SBC016 Subacute Delirium 43 0.035
714
GST071 Gastrointestinal Carcinoma 42 0.035
715
KDN007 Kidney Clear Cell Sarcoma 42 0.035
716
ALL014 Allergic Encephalomyelitis 40 0.035
717
SPN021 Spinal Meningioma 40 0.035
718
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.035
719
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.035
720
c OVR114 Ovarian Cancer 1 39 0.035
721
C1N001 C1 Inhibitor Deficiency 39 0.035
722
LVD003 Livedoid Vasculitis 39 0.035
723
SCR001 Secretory Meningioma 38 0.035
724
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.035
725
PLC009 Placenta Praevia 35 0.035
726
SPL006 Splenic Infarction 35 0.035
727
INF013 Inferior Myocardial Infarction 35 0.035
728
DLF001 Dieulafoy Lesion 35 0.035
729
CMP040 Complement Component 4, Partial Deficiency of 34 0.035
730
BRN034 Brain Meningioma 33 0.035
731
MSN003 Mesenteric Vascular Occlusion 33 0.035
733
INT053 Intracranial Vasospasm 32 0.035
734
GNT019 Giant Cell Myocarditis 30 0.035
735
UND007 Undifferentiated Connective Tissue Disease 30 0.035
736
MLL004 Mallory-Weiss Syndrome 28 0.035
737
ACT181 Acute Motor Axonal Neuropathy 27 0.035
738
JVN026 Jeavons Syndrome 24 0.035
739
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.031
740
P RTT002 Rett Syndrome 81 0.031
741
ANX010 Anxiety 75 0.031
742
FRN006 Frontotemporal Dementia 70 0.031
743
c WLM013 Wilms Tumor 1 69 0.031
744
CHL065 Cholangiocarcinoma 68 0.031
745
SKN019 Skin Melanoma 68 0.031
746
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.031
747
P SKN015 Skin Carcinoma 67 0.031
748
P CLC063 Celiac Disease 1 66 0.031
749
ACR008 Acrocallosal Syndrome 66 0.031
750
TBC004 Tobacco Addiction 65 0.031
751
P MYP004 Myopathy 63 0.031
752
P END044 Endometriosis 63 0.031
753
BLD131 Bladder Urothelial Carcinoma 62 0.031
754
P EPD009 Epidermolysis Bullosa Dystrophica 62 0.031
755
P ESP024 Esophagitis 62 0.031
756
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 62 0.031
757
P LYM033 Lymphoproliferative Syndrome 62 0.031
758
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.031
759
ORL011 Oral Cancer 62 0.031
760
THY029 Thyroid Carcinoma 62 0.031
761
APP008 Appendicitis 61 0.031
762
P CRD132 Cardiac Conduction Defect 61 0.031
763
P SCL018 Scoliosis 61 0.031
764
P CHR285 Chronic Myelomonocytic Leukemia 60 0.031
765
PNM010 Pneumothorax, Primary Spontaneous 60 0.031
766
c LPM012 Lipomatosis, Multiple 60 0.031
767
FBR047 Fibromyalgia 60 0.031
768
GST045 Gastroenteritis 60 0.031
769
c DWL002 Dowling-Degos Disease 1 59 0.031
770
c ADL017 Adult T-Cell Leukemia 59 0.031
771
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.031
772
CYT008 Cytomegalovirus Infection 58 0.031
773
GST033 Gestational Diabetes 58 0.031
774
HRP004 Herpes Zoster 58 0.031
775
ERY051 Erythroleukemia, Familial 58 0.031
776
P MTC069 Mitochondrial Disorders 57 0.031
777
SCH014 Schistosomiasis 57 0.031
778
HRY003 Hairy Cell Leukemia 57 0.031
779
APH002 Aphasia 56 0.031
780
ALV005 Alveolar Soft Part Sarcoma 56 0.031
781
P INT068 Intestinal Disease 56 0.031
782
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.031
783
P PLY019 Polyneuropathy 55 0.031
784
INT079 Intrahepatic Cholangiocarcinoma 54 0.031
785
P EPD016 Epidermolysis Bullosa 54 0.031
786
P HYP730 Hypogonadotropic Hypogonadism 54 0.031
787
TXC002 Toxic Encephalopathy 54 0.031
788
PLM017 Pulmonary Alveolar Microlithiasis 54 0.031
789
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.031
790
MSC190 Muscular Disease 54 0.031
791
P PTT006 Pituitary Adenoma 53 0.031
792
P MYM013 Moyamoya Disease 1 53 0.031
793
P MTC133 Mitochondrial Myopathy 53 0.031
794
PYD001 Pyoderma Gangrenosum 53 0.031
795
NNL006 Non-Alcoholic Steatohepatitis 53 0.031
796
c SCN007 Secondary Hyperparathyroidism 52 0.031
797
P LCT001 Lactic Acidosis 52 0.031
798
P AST007 Astrocytoma 52 0.031
799
P MSC003 Muscular Atrophy 52 0.031
800
NPH018 Nephrogenic Systemic Fibrosis 51 0.031
801
DYS014 Dyspepsia 51 0.031
802
ILS001 Ileus 51 0.031
803
PYD002 Pyoderma 51 0.031
804
CLR109 Colorectal Adenocarcinoma 51 0.031
806
c EXS019 Exostoses, Multiple, Type I 51 0.031
807
HYP080 Hypogonadism 51 0.031
808
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.031
809
c ALM001 Al Amyloidosis 50 0.031
810
P PLM006 Pulmonary Alveolar Proteinosis 50 0.031
811
P END047 Endophthalmitis 50 0.031
812
TBR011 Tuberculous Meningitis 50 0.031
813
INT253 Intestinal Benign Neoplasm 50 0.031
814
P SHR001 Short Bowel Syndrome 50 0.031
815
MTC005 Mitochondrial Metabolism Disease 50 0.031
816
PLR008 Pleurisy 50 0.031
817
c HNT010 Huntington Disease-Like 1 49 0.031
818
P RNV001 Renovascular Hypertension 49 0.031
819
P ATR005 Atrophic Gastritis 49 0.031
820
MST002 Mast-Cell Leukemia 49 0.031
821
P OBS001 Obstructive Jaundice 49 0.031
822
THR013 Thoracic Outlet Syndrome 49 0.031
823
SPL018 Splenomegaly 48 0.031
824
LYM024 Lymphatic System Disease 48 0.031
825
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.031
826
PLP001 Pulpitis 48 0.031
827
DDN010 Duodenum Cancer 47 0.031
828
AML029 Ameloblastoma 47 0.031
829
P CRN074 Coronary Artery Aneurysm 47 0.031
830
c ACQ014 Acquired Hemophilia 47 0.031
831
NCR007 Necrotizing Fasciitis 47 0.031
832
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 47 0.031
833
RTN023 Retinitis 46 0.031
834
TCL002 T-Cell Large Granular Lymphocyte Leukemia 46 0.031
835
NRR001 Neuroretinitis 46 0.031
836
GRN017 Granulocytopenia 46 0.031
837
EXT010 Extramedullary Plasmacytoma 46 0.031
838
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.031
839
LRG008 Large Granular Lymphocyte Leukemia 45 0.031
840
FBR054 Fibroma 45 0.031
841
c ACT042 Acute Pyelonephritis 44 0.031
842
c HYP272 Hypercholesterolemia, Familial, 3 44 0.031
843
BNS007 Bone Sarcoma 44 0.031
844
P VND001 Vein Disease 43 0.031
845
c SRC023 Sarcoidosis 2 43 0.031
846
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.031
847
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 43 0.031
848
c ATS069 Autosomal Dominant Optic Atrophy Plus Syndrome 43 0.031
849
TRP009 Triple X Syndrome 42 0.031
850
c NPH054 Nephrotic Syndrome, Type 3 42 0.031
851
KLD004 Keloid Disorder 41 0.031
852
SNL007 Senile Cataract 41 0.031
853
c TRC022 Tricuspid Valve Insufficiency 41 0.031
854
HYP064 Hypogonadotropism 40 0.031
855
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.031
856
LCH001 Leech Infestation 40 0.031
857
GNR003 Generalized Atherosclerosis 39 0.031
858
49X002 49,xxxxy Syndrome 39 0.031
859
MCP033 Mucopolysaccharidoses 39 0.031
860
WTR001 Waterhouse-Friderichsen Syndrome 39 0.031
861
c SYS043 Systemic Lupus Erythematosus 1 39 0.031
862
ACT056 Acute Cor Pulmonale 38 0.031
863
THR017 Thoracoabdominal Syndrome 38 0.031
864
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.031
865
c WLM011 Wilms Tumor 6 38 0.031
866
c CHR098 Chronic Pyelonephritis 38 0.031
867
c TCL024 T-Cell Non-Hodgkin Lymphoma 37 0.031
868
CHR178 Chromosomal Triplication 36 0.031
869
c DRM040 Dermatitis Herpetiformis, Familial 36 0.031
870
c CHR020 Chronic Interstitial Cystitis 36 0.031
871
PRN029 Parainfluenza Virus Type 3 35 0.031
872
ACT216 Acute Leukemia of Ambiguous Lineage 35 0.031
873
CRD016 Cardiac Rupture 33 0.031
874
CYT004 Cytomegalic Inclusion Disease 32 0.031
875
RFR002 Refractory Hairy Cell Leukemia 32 0.031
876
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.031
877
CRB198 Cerebellar Ataxia with Neuropathy and Bilateral Vestibular Areflexia Syndrome 29 0.031
878
INF118 Inflammatory Myopathy with Abundant Macrophages 29 0.031
879
CLS052 Classic Hairy Cell Leukemia 28 0.031
880
PLS031 Plastic Bronchitis 28 0.031
881
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.031
882
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.031
883
MYT019 May-Thurner Syndrome 27 0.031
884
P CLL020 Collagenopathy Type 2 Alpha 1 25 0.031
885
MSC026 Muscular Dystrophy White Matter Spongiosis 16 0.031
886
MRF001 Marfan Syndrome 75 0.025
887
c SPN225 Spondyloarthropathy 1 74 0.025
888
c HMC039 Hemochromatosis, Type 1 73 0.025
889
P MLT020 Multiple Sclerosis 73 0.025
890
VNH007 Von Hippel-Lindau Syndrome 73 0.025
891
c PRM196 Premature Ovarian Failure 1 70 0.025
892
MSC157 Muscular Dystrophy, Duchenne Type 70 0.025
893
CRB037 Cerebral Palsy 69 0.025
894
P INF038 Influenza 69 0.025
895
EWN003 Ewing Sarcoma 69 0.025
896
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.025
897
PSY004 Psychotic Disorder 68 0.025
898
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.025
899
P NRV007 Nervous System Disease 68 0.025
900
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.025
901
P LPR021 Leprosy 3 67 0.025
902
MYC006 Mycosis Fungoides 67 0.025
903
P AGM001 Agammaglobulinemia 66 0.025
904
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.025
905
SVR097 Severe Cutaneous Adverse Reaction 66 0.025
906
CHG001 Chagas Disease 66 0.025
907
P ALP004 Alport Syndrome 66 0.025
908
DSS008 Disease of Mental Health 66 0.025
909
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.025
910
P ANG001 Angelman Syndrome 65 0.025
911
FML089 Familial Thoracic Aortic Aneurysm and Dissection 65 0.025
912
LYM017 Lyme Disease 64 0.025
913
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.025
914
P TST021 Testicular Germ Cell Tumor 63 0.025
915
KHL003 Kohlschutter-Tonz Syndrome 63 0.025
916
HSH003 Hashimoto Thyroiditis 63 0.025
917
BLL006 Bullous Pemphigoid 63 0.025
918
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.025
919
PCK003 Pick Disease of Brain 63 0.025
920
PPL049 Papillon-Lefevre Syndrome 63 0.025
921
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.025
922
MCR013 Microphthalmia 62 0.025
923
LYM012 Lymphoplasmacytic Lymphoma 62 0.025
924
BRC012 Brucellosis 62 0.025
925
P DRM010 Dermatomyositis 62 0.025
926
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.025
927
INT066 Interstitial Lung Disease 61 0.025
928
CHR066 Chronic Fatigue Syndrome 61 0.025
930
MSL001 Measles 61 0.025
931
c ANM038 Anemia, Autoimmune Hemolytic 61 0.025
932
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.025
933
GNG013 Gingivitis 60 0.025
934
PRT058 Pure Autonomic Failure 60 0.025
935
ART001 Arterial Tortuosity Syndrome 60 0.025
936
CHR072 Chordoma 60 0.025
937
LPT001 Leptospirosis 60 0.025
938
BRN002 Bronchiolitis 60 0.025
939
P RHN004 Rhinitis 59 0.025
940
FCT002 Factor Xi Deficiency 59 0.025
941
DNG002 Dengue Hemorrhagic Fever 59 0.025
942
ANG020 Angiosarcoma 59 0.025
943
SZR001 Sezary's Disease 59 0.025
944
IRN001 Iron Deficiency Anemia 59 0.025
945
c MST023 Mesothelioma, Malignant 59 0.025
946
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.025
947
ADR005 Adrenal Carcinoma 58 0.025
948
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 58 0.025
949
EXT034 Extrinsic Allergic Alveolitis 58 0.025
950
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.025
951
P TRC086 Trichohepatoenteric Syndrome 1 57 0.025
952
BRN056 Bronchopulmonary Dysplasia 57 0.025
953
RSP006 Respiratory System Disease 57 0.025
954
ACT200 Acute Monoblastic Leukemia 56 0.025
955
ALL010 Allergic Contact Dermatitis 56 0.025
956
APH001 Aphthous Stomatitis 56 0.025
957
CMR002 Coumarin Resistance 56 0.025
958
P RTN016 Retinal Degeneration 56 0.025
959
c CNT035 Central Nervous System Disease 56 0.025
960
MTH009 Mouth Disease 56 0.025
961
MYP139 Myopathy, Proximal, and Ophthalmoplegia 56 0.025
962
c PRD040 Periodontitis, Chronic 56 0.025
963
P LTR001 Lateral Sclerosis 56 0.025
964
SNS003 Sensory Peripheral Neuropathy 56 0.025
965
DBL002 Double Outlet Right Ventricle 55 0.025
966
P PNM006 Pneumoconiosis 55 0.025
967
SYN007 Synovitis 55 0.025
968
SLC006 Silicosis 55 0.025
969
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
970
MXD005 Mixed Connective Tissue Disease 55 0.025
971
PST046 Post-Transplant Lymphoproliferative Disease 55 0.025
972
ORL004 Oral Submucous Fibrosis 55 0.025
973
RHM028 Rheumatic Heart Disease 54 0.025
974
FCT004 Factor Xii Deficiency 54 0.025
975
P LYM025 Lymphedema 54 0.025
976
c MCP043 Mucopolysaccharidosis, Type Iiia 54 0.025
977
PNC001 Pancytopenia 54 0.025
978
P SLM003 Salmonellosis 54 0.025
979
P PNC025 Panic Disorder 53 0.025
980
P PTS002 Ptosis 53 0.025
981
P CHL066 Cholangitis 53 0.025
982
SPS003 Spastic Diplegia 53 0.025
983
PGM001 Pigmented Villonodular Synovitis 52 0.025
984
PRT129 Prothrombin Deficiency, Congenital 52 0.025
985
P THY032 Thyroiditis 52 0.025
986
DNT012 Dental Caries 52 0.025
987
INT303 Intracranial Hypertension, Idiopathic 52 0.025
988
P TRT010 Teratoma 52 0.025
989
P CHR345 Chronic Pain 52 0.025
990
P SML016 Small Intestine Cancer 51 0.025
991
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.025
992
QDR001 Quadriplegia 51 0.025
993
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.025
994
URC002 Urea Cycle Disorder 51 0.025
995
ADR016 Adrenal Cortical Carcinoma 51 0.025
996
CRY003 Cryptosporidiosis 50 0.025
997
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.025
998
ATY042 Atypical Chronic Myeloid Leukemia 50 0.025
999
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.025
1000
MNN009 Meningoencephalitis 50 0.025
1001
TST044 Testicular Torsion 49 0.025
1002
P CRN028 Corneal Ulcer 49 0.025
1003
CHR563 Chronic Eosinophilic Leukemia 49 0.025
1004
BHV002 Behavioral Variant of Frontotemporal Dementia 49 0.025
1005
P END046 Endometritis 49 0.025
1006
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.025
1007
PST062 Pustulosis Palmaris Et Plantaris 48 0.025
1008
P PLN008 Peeling Skin Syndrome 48 0.025
1009
EWN002 Ewing's Family of Tumors 48 0.025
1010
SPT005 Spotted Fever 48 0.025
1011
ATN005 Autonomic Dysfunction 48 0.025
1012
MYL001 Myelitis 48 0.025
1013
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.025
1014
HYP017 Hypophosphatemia 48 0.025
1015
RYN001 Raynaud Disease 48 0.025
1016
P TRN034 Transverse Myelitis 48 0.025
1017
BRN014 Bronchopneumonia 47 0.025
1018
ORL013 Oral Lichen Planus 47 0.025
1019
PTT037 Pituitary Tumors 47 0.025
1020
P ART018 Aortic Valve Insufficiency 47 0.025
1021
P LPC002 Lip Cancer 47 0.025
1022
CRY004 Cryoglobulinemia 47 0.025
1023
MCR191 Microscopic Colitis 47 0.025
1024
P BNG032 Benign Mesothelioma 47 0.025
1025
c VRL012 Viral Meningitis 47 0.025
1026
LYM051 Lymphomatoid Granulomatosis 47 0.025
1027
ART004 Aortic Atherosclerosis 47 0.025
1028
URT010 Ureteral Obstruction 46 0.025
1029
KRT008 Keratopathy 46 0.025
1030
ANT018 Anthracosis 46 0.025
1031
EXT033 Extrapulmonary Tuberculosis 46 0.025
1032
FML039 Female Reproductive System Disease 46 0.025
1033
PRS063 Paresthesia 46 0.025
1034
PPL021 Papilledema 46 0.025
1035
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 45 0.025
1036
INT054 Intraocular Lymphoma 45 0.025
1037
TND005 Tendinitis 45 0.025
1038
MYC005 Myocardial Stunning 45 0.025
1039
P OCY003 Oocyte Maturation Defect 1 44 0.025
1040
MCL003 Macular Holes 44 0.025
1041
LPP002 Lipoprotein Glomerulopathy 44 0.025
1042
P ERY008 Erythromelalgia 44 0.025
1043
ADR004 Adrenal Cortical Adenocarcinoma 44 0.025
1044
BNS003 Binswanger's Disease 43 0.025
1045
PRL008 Paralytic Ileus 43 0.025
1046
ANC002 Anca-Associated Vasculitis 43 0.025
1047
MCR011 Microinvasive Gastric Cancer 43 0.025
1048
DFF003 Diffuse Scleroderma 43 0.025
1049
c HMG001 Hemoglobin C Disease 43 0.025
1050
CYS009 Cystadenoma 43 0.025
1051
OVR112 Ovarian Germ Cell Cancer 43 0.025
1052
ART006 Arthus Reaction 43 0.025
1053
ORL012 Oral Leukoplakia 42 0.025
1054
c HYP072 Hypersensitivity Reaction Type Iii Disease 42 0.025
1055
ACT088 Acute Insulin Response 42 0.025
1056
c CHR576 Chronic Beryllium Disease 42 0.025
1057
CRD003 Cardiac Sarcoidosis 42 0.025
1058
P PLM025 Pulmonary Venoocclusive Disease 42 0.025
1059
KRN001 Korean Hemorrhagic Fever 42 0.025
1060
PRM013 Premature Menopause 41 0.025
1061
CLP006 Clopidogrel Resistance 41 0.025
1062
MYX004 Myxedema 41 0.025
1063
BRY001 Berylliosis 41 0.025
1064
LKP003 Leukoplakia 40 0.025
1065
UTR043 Uterine Sarcoma 40 0.025
1066
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 40 0.025
1067
P TST026 Testicular Germ Cell Cancer 40 0.025
1068
P BRY005 Beryllium Disease 40 0.025
1070
IMM001 Immune-Complex Glomerulonephritis 40 0.025
1071
c ATM075 Autoimmune Encephalitis 39 0.025
1072
OVR094 Ovarian Epithelial Cancer 39 0.025
1073
PLX004 Plexopathy 39 0.025
1074
c HRD104 Hereditary Multiple Osteochondromas 39 0.025
1075
EXT006 Extrahepatic Cholestasis 38 0.025
1076
FRN014 Fournier Gangrene 38 0.025
1077
TRP005 Trophoblastic Neoplasm 38 0.025
1078
c PLY105 Polycystic Ovary Syndrome 1 38 0.025
1079
STR077 Streptococcal Toxic-Shock Syndrome 38 0.025
1080
ACT040 Acute Poststreptococcal Glomerulonephritis 37 0.025
1081
c RTN050 Retinitis Pigmentosa 20 37 0.025
1082
IRT001 Iritis