Search results for Heparin

1634 hits were found for Heparin

# Family MCID Name MIFTS Score
1
HPR006 Heparin Cofactor Ii Deficiency 40 8.673
2
HPR003 Heparin-Induced Thrombocytopenia 48 7.885
3
P THR014 Thrombocytopenia 67 1.019
4
c THR092 Thrombophilia Due to Thrombin Defect 73 0.669
5
PLM033 Pulmonary Embolism 59 0.581
6
THR024 Thrombosis 57 0.552
7
INT007 Intermediate Coronary Syndrome 55 0.349
8
ISC004 Ischemia 58 0.305
9
DSS009 Disseminated Intravascular Coagulation 57 0.284
10
c ACT075 Acute Myocardial Infarction 57 0.284
11
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.283
12
P MYC007 Myocardial Infarction 70 0.250
13
P THR015 Thrombophilia 51 0.235
14
P KDN018 Kidney Disease 72 0.232
15
P ANT006 Antiphospholipid Syndrome 55 0.212
16
LPP008 Lipoprotein Quantitative Trait Locus 62 0.212
17
ANG054 Angina Pectoris 66 0.206
18
c PRC016 Pre-Eclampsia 63 0.200
19
ALL026 Allergic Hypersensitivity Disease 62 0.195
20
P VSC007 Vascular Disease 63 0.190
21
THR016 Thrombophlebitis 51 0.190
22
END086 End Stage Renal Disease 51 0.190
23
STR067 Stroke, Ischemic 81 0.189
24
48X005 48,xyyy 39 0.184
25
c ACT071 Acute Kidney Failure 60 0.182
26
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.181
27
ART140 Arteries, Anomalies of 52 0.176
28
ATH013 Atherosclerosis Susceptibility 65 0.174
29
c CHR684 Chronic Kidney Disease 70 0.158
30
P OST002 Osteoporosis 74 0.150
31
TXC005 Toxic Shock Syndrome 62 0.149
32
LMB062 Limb Ischemia 55 0.149
33
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.149
34
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.149
35
P GLM007 Glomerulonephritis 57 0.148
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.146
37
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.146
38
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.145
39
P CRN300 Coronary Heart Disease 1 63 0.145
40
PRP027 Peripheral Vascular Disease 71 0.144
41
P ART021 Arteriosclerosis 54 0.144
42
P ATR011 Atrial Fibrillation 66 0.143
43
CRB039 Cerebrovascular Disease 67 0.142
44
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.141
45
P PLM037 Pulmonary Hypertension 67 0.138
46
PLC008 Placenta Disease 50 0.138
47
CRN017 Coronary Thrombosis 47 0.138
48
P CRD119 Cardiac Arrest 67 0.136
49
LVR012 Liver Cirrhosis 62 0.136
50
PRP030 Purpura 54 0.135
51
ART016 Aortic Aneurysm 69 0.133
52
ANT009 Antithrombin Iii Deficiency 59 0.133
53
CRD137 Cardiogenic Shock 47 0.133
54
P HYP750 Hypertriglyceridemia, Familial 62 0.131
55
P ECL001 Eclampsia 50 0.130
56
MST004 Mast Cell Neoplasm 42 0.129
57
CYT002 Cytokine Deficiency 42 0.129
58
EXT007 Extracutaneous Mastocytoma 38 0.129
59
c ACT027 Acute Pancreatitis 60 0.127
60
ANR040 Aneurysm 59 0.125
61
P RSP003 Respiratory Failure 74 0.121
62
c HYP836 Hypercholesterolemia, Familial, 1 73 0.120
63
ULC004 Ulcerative Colitis 73 0.120
64
SPN186 Spinal Cord Injury 60 0.120
65
CVD001 Covid-19 44 0.120
66
P CLR023 Colorectal Cancer 99 0.119
67
PRT036 Peritonitis 64 0.119
68
CLT003 Colitis 62 0.116
69
P LVR013 Liver Disease 68 0.114
70
P PST095 Post-Thrombotic Syndrome 51 0.114
71
P PNC044 Pancreatitis 61 0.112
72
P CTR002 Cataract 60 0.112
73
BNR002 Bone Resorption Disease 48 0.112
74
P NPH012 Nephrotic Syndrome 60 0.111
75
P HRT032 Heart Disease 75 0.110
76
HLX001 Helix Syndrome 47 0.110
77
P OVR042 Ovarian Cancer 88 0.108
78
c SYS001 Systemic Lupus Erythematosus 86 0.108
79
P END033 Endocarditis 57 0.108
80
47X002 47,xyy 49 0.108
81
TRN015 Transient Cerebral Ischemia 63 0.107
82
P INT143 Interstitial Cystitis 61 0.107
83
P CYS018 Cystitis 59 0.107
84
PLM010 Pulmonary Edema 54 0.105
85
DRM006 Dermatitis 61 0.104
86
P INF032 Infertility 57 0.104
87
HPT046 Hepatic Veno-Occlusive Disease 56 0.104
88
c SVR005 Severe Pre-Eclampsia 50 0.104
89
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.104
90
P PNC035 Pancreatic Cancer 84 0.103
91
PNG002 Pain Agnosia 51 0.103
92
P NTR004 Neutropenia 63 0.101
93
VTM033 Vitamin K Deficiency Bleeding 48 0.101
94
c RHB024 Rhabdomyosarcoma 2 67 0.100
95
P LPS004 Lupus Erythematosus 61 0.100
96
PRT018 Portal Vein Thrombosis 50 0.100
97
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.098
98
c MCR113 Microvascular Complications of Diabetes 3 52 0.098
99
THR004 Thrombocytosis 51 0.098
100
c MCR120 Microvascular Complications of Diabetes 7 47 0.098
101
c MCR130 Microvascular Complications of Diabetes 6 41 0.098
102
c MCR133 Microvascular Complications of Diabetes 4 41 0.098
103
c SVR001 Severe Acute Respiratory Syndrome 62 0.096
104
ATM095 Autoimmune Disease 62 0.095
105
DPH001 Diphtheria 60 0.095
106
PLC007 Placental Abruption 48 0.095
107
P LNG032 Lung Cancer 98 0.093
108
P BRS047 Breast Cancer 97 0.093
109
DFC004 Deficiency Anemia 70 0.093
110
CNG034 Congestive Heart Failure 69 0.093
111
P VSC011 Vasculitis 62 0.093
112
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.092
113
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.092
114
P PRG092 Pregnancy Loss, Recurrent 1 40 0.092
115
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.090
116
VRC005 Varicose Veins 60 0.090
117
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.088
118
c FML001 Familial Atrial Fibrillation 65 0.088
119
P ADL010 Adult Respiratory Distress Syndrome 65 0.088
120
P NRB001 Neuroblastoma 72 0.087
121
P AMY004 Amyloidosis 70 0.087
122
P ADN016 Adenocarcinoma 64 0.087
123
P URT039 Urticaria 58 0.087
124
P INF037 Inflammatory Bowel Disease 54 0.087
125
P HPT023 Hepatocellular Carcinoma 100 0.085
126
P PNM007 Pneumonia 68 0.085
127
P HML002 Hemolytic Anemia 63 0.085
128
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.085
129
PRN019 Perinatal Necrotizing Enterocolitis 59 0.085
130
BCT022 Bacterial Infectious Disease 56 0.085
131
ENT011 Enterocolitis 51 0.085
132
P VTR007 Vitreoretinopathy 46 0.085
133
c HYP595 Hypertension, Essential 84 0.083
134
DWN001 Down Syndrome 70 0.083
135
P GLM045 Glioma 63 0.083
136
P CRD246 Cardiovascular System Disease 57 0.083
137
PRT011 Protein C Deficiency 44 0.083
138
MYL069 Myeloma, Multiple 85 0.081
139
GLB015 Glioblastoma Multiforme 75 0.081
140
ADL002 Adult Syndrome 70 0.081
141
NTR005 Nutritional Deficiency Disease 62 0.081
142
BRN071 Brain Injury 49 0.081
143
c PRM038 Primary Agammaglobulinemia 44 0.081
144
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.081
145
P GST053 Gastric Cancer 83 0.079
146
P TRN020 Turner Syndrome 67 0.079
147
P MCR115 Microvascular Complications of Diabetes 5 66 0.079
148
P HRP006 Herpes Simplex 65 0.079
149
INT002 Intermittent Claudication 61 0.079
150
P CMP008 Compartment Syndrome 49 0.079
151
GLL048 Glial Tumor 45 0.079
152
ATX019 Ataxia with Vitamin E Deficiency 42 0.079
153
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.077
154
P MLN008 Melanoma 69 0.077
155
P HYP098 Hypereosinophilic Syndrome 67 0.077
156
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.077
157
P PSR002 Psoriasis 62 0.077
158
HYP066 Hyperglycemia 61 0.077
159
RTN017 Retinal Detachment 61 0.077
160
P UVT001 Uveitis 57 0.077
161
P NRP001 Neuropathy 56 0.077
162
PRP080 Peripheral Artery Disease 53 0.077
163
PRP016 Paraplegia 52 0.077
164
PST011 Pustulosis of Palm and Sole 52 0.077
165
TRM010 Traumatic Brain Injury 51 0.077
166
MTB004 Metabolic Acidosis 50 0.077
167
VCC001 Vaccinia 49 0.077
168
PRT014 Protein S Deficiency 44 0.077
170
P LKM062 Leukemia, Acute Lymphoblastic 69 0.076
171
P ESS003 Essential Thrombocythemia 68 0.076
172
P DBT009 Diabetes Mellitus 64 0.076
173
LNG099 Lung Disease 60 0.076
174
P EXN002 Exanthem 57 0.076
175
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.076
176
PLC005 Placental Insufficiency 57 0.076
177
P VNS003 Venous Insufficiency 55 0.076
178
INF034 Infective Endocarditis 53 0.076
179
P HMP007 Hemophilia 51 0.076
180
P BCT020 Bacteremia 2 44 0.076
181
P PRS040 Prostate Cancer 97 0.074
182
HMN044 Human Immunodeficiency Virus Type 1 71 0.074
183
P PLM036 Pulmonary Fibrosis 65 0.074
184
c DBT099 Diabetes Mellitus, Type I 65 0.074
185
ACT119 Acute Promyelocytic Leukemia 63 0.074
186
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.074
187
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.074
188
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.074
189
OCL069 Ocular Motor Apraxia 51 0.074
190
P SCK005 Sickle Cell Disease 50 0.074
191
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.074
192
PRP007 Priapism 47 0.074
193
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.074
194
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.074
195
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.074
196
HDN002 Head Injury 46 0.074
197
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.074
198
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.074
199
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.074
200
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.074
201
P HYP120 Hypoaldosteronism 36 0.074
202
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.074
203
P LKM002 Leukemia 68 0.071
204
P MNN013 Meningitis 66 0.071
205
CLN015 Colon Adenocarcinoma 65 0.071
206
c ACT134 Acute Liver Failure 56 0.071
207
HRT011 Heart Septal Defect 50 0.071
208
CRB086 Cerebral Aneurysms 40 0.071
209
CYS001 Cystic Fibrosis 81 0.069
210
OST012 Osteoarthritis 78 0.069
211
LPT014 Leptin Deficiency or Dysfunction 74 0.069
212
c FML021 Familial Hypercholesterolemia 66 0.069
213
c SML038 Small Cell Cancer of the Lung 65 0.069
214
BDD001 Budd-Chiari Syndrome 63 0.069
215
LPD008 Lipid Metabolism Disorder 62 0.069
216
PRT013 Portal Hypertension 59 0.069
217
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.069
218
P PLY018 Polycythemia 56 0.069
219
P HML001 Hemolytic-Uremic Syndrome 53 0.069
220
ART074 Aortic Dissection 52 0.069
221
P MTR003 Mitral Valve Stenosis 50 0.069
222
P PRP034 Purpura Fulminans 43 0.069
223
P BLD134 Bladder Cancer 79 0.067
224
AST005 Asthma 76 0.067
225
OST159 Osteogenic Sarcoma 66 0.067
226
c ACT068 Acute Cystitis 63 0.067
227
P BRS044 Breast Adenocarcinoma 59 0.067
228
GST023 Gastric Ulcer 53 0.067
229
INT078 Intracranial Thrombosis 49 0.067
230
URM002 Uremia 49 0.067
231
CRB004 Cerebral Artery Occlusion 45 0.067
232
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.067
233
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.067
234
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.065
235
IMM167 Immune Deficiency Disease 78 0.065
236
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.065
237
P MST009 Mastocytosis 64 0.065
238
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.065
239
P MYL006 Myeloid Leukemia 60 0.065
240
SQM006 Squamous Cell Carcinoma 60 0.065
241
INT030 Intracranial Aneurysm 56 0.065
242
c HNT004 Huntington Disease-Like 2 50 0.065
243
HMG002 Hemoglobinuria 50 0.065
244
INT010 Intracranial Embolism 48 0.065
245
STN005 St Anthony's Fire 17 0.065
246
c LKM061 Leukemia, Acute Myeloid 84 0.062
247
MLR004 Malaria 81 0.062
248
BRN024 Bronchitis 68 0.062
249
P ATR010 Atrial Heart Septal Defect 60 0.062
250
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.062
251
P LCH002 Lichen Planus 53 0.062
252
XNT003 Xanthomatosis 49 0.062
253
CRN027 Corneal Neovascularization 47 0.062
254
LYM019 Lymphosarcoma 46 0.062
255
PRT019 Protein-Losing Enteropathy 45 0.062
256
c HNT011 Huntington Disease-Like 3 38 0.062
257
P ALZ034 Alzheimer Disease 88 0.060
258
INS024 Insulin-Like Growth Factor I 79 0.060
259
PLY001 Polycythemia Vera 69 0.060
260
PLM001 Pulmonary Tuberculosis 69 0.060
261
PNC129 Pancreatic Adenocarcinoma 68 0.060
262
SRC014 Sarcoma 65 0.060
263
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.060
264
P HMN010 Hemangioma 61 0.060
265
P MYC008 Myocarditis 59 0.060
266
c HPT016 Hepatitis B 59 0.060
267
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.060
268
P FBR017 Fibrosarcoma 56 0.060
269
ALL006 Allergic Asthma 56 0.060
270
ACT058 Active Peptic Ulcer Disease 55 0.060
271
HLL004 Hellp Syndrome 54 0.060
272
P HMR003 Hemorrhagic Disease 53 0.060
273
SPN035 Spindle Cell Sarcoma 53 0.060
274
STM007 Stomatitis 50 0.060
275
c CHR431 Chronic Venous Insufficiency 49 0.060
276
c MTR002 Mitral Valve Insufficiency 48 0.060
277
CRD001 Cardiac Tamponade 47 0.060
278
c THR037 Thrombocytopenia 2 40 0.060
279
SHW001 Shwartzman Phenomenon 37 0.060
280
LYM005 Lymphocele 35 0.060
281
P RHM011 Rheumatoid Arthritis 80 0.057
282
c DLT002 Dilated Cardiomyopathy 79 0.057
283
P LNG064 Lung Cancer Susceptibility 3 78 0.057
284
P OCL013 Oculodentodigital Dysplasia 69 0.057
285
P LYM118 Lymphoma 68 0.057
286
PRT037 Pertussis 65 0.057
287
c PNS012 Paine Syndrome 61 0.057
288
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.057
289
NWB001 Newborn Respiratory Distress Syndrome 58 0.057
290
IRN002 Iron Metabolism Disease 57 0.057
291
HYP266 Hypoxia 57 0.057
292
HYP060 Hyperinsulinism 54 0.057
293
PRS045 Prostatic Hypertrophy 53 0.057
294
c GLL024 Gallbladder Disease 1 53 0.057
295
BWN001 Bowen-Conradi Syndrome 52 0.057
296
FCT001 Factor Viii Deficiency 51 0.057
297
BCK006 Back Pain 42 0.057
298
ANX004 Anoxia 40 0.057
299
c ACQ005 Acquired Thrombocytopenia 39 0.057
300
THR123 Thrombotic Microangiopathy 36 0.057
301
SGT001 Sagittal Sinus Thrombosis 32 0.057
302
FMR003 Femoral Neuropathy 31 0.057
304
P LKM071 Leukemia, Chronic Lymphocytic 79 0.055
305
SVR004 Severe Combined Immunodeficiency 73 0.055
306
P PHC003 Pheochromocytoma 71 0.055
307
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.055
308
c HYP768 Hyperlipoproteinemia, Type I 67 0.055
309
P HPT021 Hepatitis 67 0.055
310
c MCR129 Microvascular Complications of Diabetes 1 66 0.055
311
c BRN108 Branchiootic Syndrome 1 62 0.055
312
ACQ007 Acquired Immunodeficiency Syndrome 60 0.055
313
RHM001 Rheumatic Fever 60 0.055
314
CNT047 Contact Dermatitis 58 0.055
315
LYM027 Lymphopenia 58 0.055
316
P HDC001 Headache 57 0.055
317
P ANG015 Angioedema 57 0.055
318
P PYL005 Pyelonephritis 56 0.055
319
AGN016 Aging 56 0.055
320
CHR100 Chronic Ulcer of Skin 55 0.055
321
P ALP008 Alopecia 54 0.055
322
HRT012 Heart Valve Disease 53 0.055
323
P RTN022 Retinal Vein Occlusion 53 0.055
324
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.055
325
P RCT021 Rectum Cancer 52 0.055
326
LNG031 Lung Benign Neoplasm 51 0.055
327
PRS129 Prostatic Hyperplasia, Benign 49 0.055
328
c ACT150 Acute Adrenal Insufficiency 48 0.055
329
HMP001 Hemopericardium 48 0.055
330
P BLD051 Blood Coagulation Disease 46 0.055
331
ADR040 Adrenal Gland Pheochromocytoma 46 0.055
332
c MLG068 Malignant Glioma 46 0.055
333
HMR002 Hemarthrosis 45 0.055
334
MDD018 Middle East Respiratory Syndrome 43 0.055
335
c MCR112 Microvascular Complications of Diabetes 2 41 0.055
336
c SBC003 Subacute Bacterial Endocarditis 33 0.055
337
P GLM040 Glioma Susceptibility 1 81 0.052
338
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.052
339
CNN005 Connective Tissue Disease 68 0.052
340
HYP056 Hypoglycemia 66 0.052
341
P ART005 Arteriovenous Malformation 65 0.052
342
OST017 Osteomyelitis 64 0.052
343
P RHB003 Rhabdomyosarcoma 63 0.052
344
SKN016 Skin Disease 63 0.052
345
P ENC018 Encephalopathy 61 0.052
346
ING001 Inguinal Hernia 60 0.052
347
c HRD002 Hereditary Angioedema 60 0.052
348
P BRN019 Bernard-Soulier Syndrome 60 0.052
349
CHL014 Cholera 59 0.052
350
c ACT073 Acute Leukemia 58 0.052
351
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.052
352
MCS002 Mucositis 56 0.052
353
BRN004 Brain Edema 56 0.052
354
P GST044 Gastritis 56 0.052
355
PRS021 Prostatic Adenoma 51 0.052
356
CLC001 Calciphylaxis 51 0.052
357
P RTN014 Retinal Artery Occlusion 47 0.052
358
CYN002 Cyanosis, Transient Neonatal 45 0.052
359
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.052
360
BRN026 Branch Retinal Artery Occlusion 40 0.052
361
MNN021 Meningococcemia 37 0.052
362
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.052
363
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.052
364
ESP021 Esophageal Cancer 90 0.049
365
END057 Endometrial Cancer 74 0.049
366
SCK003 Sickle Cell Anemia 74 0.049
367
c HPT073 Hepatitis C Virus 72 0.049
368
P SRC025 Sarcoidosis 1 70 0.049
369
P ART022 Arthritis 69 0.049
370
P HYP086 Hypothyroidism 69 0.049
371
c HMP004 Hemophilia B 68 0.049
372
BRK010 Burkitt Lymphoma 67 0.049
373
c MGR028 Migraine with or Without Aura 1 67 0.049
374
ALC007 Alcohol Dependence 66 0.049
375
AFB002 Afibrinogenemia, Congenital 65 0.049
376
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.049
377
c ART101 Aortic Valve Disease 2 65 0.049
378
c FNC043 Fanconi Anemia, Complementation Group E 62 0.049
379
CRC021 Carcinosarcoma 62 0.049
380
P ENC004 Encephalitis 61 0.049
381
PTN001 Patent Foramen Ovale 60 0.049
382
P VNT002 Ventricular Septal Defect 60 0.049
383
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.049
384
P BCL017 B-Cell Lymphoma 58 0.049
385
PNM008 Pneumothorax 56 0.049
386
SFT003 Soft Tissue Sarcoma 56 0.049
387
P HYP076 Hyperthyroidism 55 0.049
388
HMP005 Hemiplegia 55 0.049
389
P PMP001 Pemphigus 54 0.049
390
AMN003 Amnestic Disorder 54 0.049
391
GSG001 Gas Gangrene 53 0.049
392
c VRL010 Viral Hepatitis 52 0.049
393
ESP002 Esophageal Varix 51 0.049
394
P PRC012 Pericardial Effusion 51 0.049
395
CRN030 Coronary Stenosis 50 0.049
396
ENT004 Enthesopathy 49 0.049
397
RYN005 Raynaud Phenomenon 47 0.049
398
SYN036 Syncope 45 0.049
399
TRT001 Teratocarcinoma 45 0.049
400
DBT008 Diabetic Angiopathy 44 0.049
401
P PRL003 Proliferative Glomerulonephritis 44 0.049
402
DRG024 Drug Allergy 42 0.049
403
THR035 Thrombasthenia 40 0.049
404
PRT012 Prothrombin Deficiency 40 0.049
405
c CHR682 Chronic Bilirubin Encephalopathy 39 0.049
406
P PRC031 Preeclampsia/eclampsia 1 38 0.049
407
c MYC058 Myocardial Infarction 2 34 0.049
408
ARG004 Argyria 27 0.049
409
CHL079 Children's Interstitial Lung Disease 26 0.049
410
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.046
411
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.046
412
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.046
413
P CNR004 Cone-Rod Dystrophy 2 73 0.046
414
MST024 Mastocytosis, Cutaneous 69 0.046
415
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.046
416
MYL031 Myeloproliferative Neoplasm 66 0.046
417
P CNJ013 Conjunctivitis 65 0.046
418
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.046
419
P BND020 Bone Disease 59 0.046
420
SPN027 Spinal Stenosis 59 0.046
421
TRN018 Transitional Cell Carcinoma 56 0.046
422
c FML035 Familial Hyperlipidemia 55 0.046
423
HYP005 Hypokalemia 55 0.046
424
NPH009 Nephrolithiasis 55 0.046
425
HMC014 Homocysteinemia 53 0.046
426
OLG003 Oligohydramnios 51 0.046
427
BHR001 Behr Syndrome 51 0.046
428
HYP081 Hypolipoproteinemia 51 0.046
429
P OVR082 Overgrowth Syndrome 50 0.046
430
CRT013 Carotid Stenosis 50 0.046
431
c INF145 Infantile Liver Failure Syndrome 1 50 0.046
432
BLD053 Blood Platelet Disease 49 0.046
433
CLC006 Calcinosis 48 0.046
434
IGG001 Iga Glomerulonephritis 48 0.046
435
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.046
436
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.046
437
P OVR046 Ovarian Cyst 47 0.046
438
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.046
439
LPD004 Lipoid Nephrosis 46 0.046
440
ORL015 Oral Squamous Cell Carcinoma 43 0.046
441
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.046
442
PRS063 Paresthesia 41 0.046
443
P MLG074 Malignant Mesenchymoma 40 0.046
444
ART008 Arteriosclerosis Obliterans 40 0.046
445
CRT004 Carotid Artery Thrombosis 38 0.046
446
MRN001 Marantic Endocarditis 38 0.046
447
GLM044 Glomerular Disease 37 0.046
448
P ANT001 Anterolateral Myocardial Infarction 34 0.046
449
CRT008 Carotid Artery Dissection 33 0.046
450
SNG003 Single Ventricular Heart 30 0.046
452
INT076 Intracranial Sinus Thrombosis 29 0.046
453
P APL001 Aplastic Anemia 74 0.042
454
BRN028 Brain Cancer 74 0.042
455
P GRF003 Graft-Versus-Host Disease 72 0.042
456
MYL005 Myelofibrosis 70 0.042
457
P TTR001 Tetralogy of Fallot 70 0.042
458
LYM133 Lymphoma, Hodgkin, Classic 69 0.042
459
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.042
460
P INF038 Influenza 68 0.042
461
P NSP012 Nasopharyngeal Carcinoma 66 0.042
462
P VNW001 Von Willebrand's Disease 65 0.042
463
KWS002 Kawasaki Disease 65 0.042
464
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.042
465
P PRD008 Periodontitis 64 0.042
466
MSC007 Muscle Hypertrophy 64 0.042
467
LSH001 Leishmaniasis 63 0.042
468
DPR016 Depression 63 0.042
469
HMT002 Hematologic Cancer 62 0.042
470
P ESP024 Esophagitis 62 0.042
471
CHL068 Cholestasis 61 0.042
472
VRL011 Viral Infectious Disease 61 0.042
473
P THL005 Thalassemia 60 0.042
474
CHL123 Chlamydia 59 0.042
475
P DNG005 Dengue Virus 59 0.042
476
PPT005 Peptic Ulcer Disease 59 0.042
477
SPT004 Septic Arthritis 58 0.042
478
P ALC033 Alcohol Use Disorder 58 0.042
479
PMP006 Pemphigus Vulgaris, Familial 57 0.042
480
GLS018 Glass Syndrome 57 0.042
481
VSC002 Vascular Dementia 57 0.042
482
HMR039 Hemorrhage, Intracerebral 57 0.042
483
P PLY011 Polycystic Ovary Syndrome 56 0.042
484
EMB004 Embryonal Carcinoma 56 0.042
485
MCL006 Macular Retinal Edema 55 0.042
486
P DRR001 Diarrhea 55 0.042
487
c BCT007 Bacterial Meningitis 55 0.042
488
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.042
489
INT075 Intracranial Hypertension 53 0.042
490
PLS007 Plasmodium Falciparum Malaria 52 0.042
491
MRG003 Marginal Zone B-Cell Lymphoma 52 0.042
492
c VRL005 Viral Pneumonia 52 0.042
493
SPL004 Splenic Marginal Zone Lymphoma 51 0.042
494
ACT017 Acute Chest Syndrome 51 0.042
495
P MMB011 Membranous Nephropathy 50 0.042
496
ERY004 Erysipelas 49 0.042
497
BLD044 Bladder Disease 48 0.042
498
P UTR058 Uterine Anomalies 47 0.042
499
MNN020 Meningococcal Infection 46 0.042
500
URL001 Urolithiasis 45 0.042
501
BCT021 Bacterial Sepsis 44 0.042
502
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.042
503
c CNT028 Central Retinal Artery Occlusion 43 0.042
504
TRP009 Triple X Syndrome 42 0.042
505
GST020 Gastric Antral Vascular Ectasia 41 0.042
506
P KLZ004 Kala-Azar 1 41 0.042
507
SPR126 Superior Semicircular Canal Dehiscence 40 0.042
508
c HMG029 Hemoglobin Se Disease 39 0.042
509
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.042
510
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.042
511
LGN005 Ligneous Conjunctivitis 31 0.042
512
URN022 Urinary Tract Infections, Recurrent 27 0.042
513
HYP736 Hyperheparinemia 12 0.042
514
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.039
515
c ATR087 Atrial Standstill 1 75 0.039
516
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.039
517
CRT072 Creutzfeldt-Jakob Disease 70 0.039
518
MNT001 Mantle Cell Lymphoma 69 0.039
519
P SYS005 Systemic Scleroderma 68 0.039
520
CHL065 Cholangiocarcinoma 68 0.039
521
P MYS003 Myasthenia Gravis 68 0.039
522
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.039
523
P FLL037 Follicular Lymphoma 67 0.039
524
c HMP029 Hemophilia a 67 0.039
525
P MSC005 Muscular Dystrophy 66 0.039
526
TTN003 Tetanus 65 0.039
527
KRT019 Keratitis, Hereditary 65 0.039
528
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.039
529
GT001 Gout 64 0.039
530
MGK001 Megakaryocytic Leukemia 64 0.039
531
c DPH024 Diaphragmatic Hernia, Congenital 63 0.039
532
P HYP069 Hyperparathyroidism 63 0.039
533
P HYP055 Hypoplastic Left Heart Syndrome 63 0.039
534
P LMY004 Leiomyosarcoma 63 0.039
535
c HPT001 Hepatitis C 62 0.039
536
FTT001 Fatty Liver Disease 61 0.039
537
c SCL052 Scleroderma, Familial Progressive 61 0.039
538
GST033 Gestational Diabetes 61 0.039
539
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.039
540
P KDN017 Kidney Cancer 60 0.039
541
P SNS001 Sensorineural Hearing Loss 60 0.039
542
CHC001 Chickenpox 60 0.039
543
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.039
544
ADN018 Adenoma 59 0.039
545
P ANP001 Anaplastic Large Cell Lymphoma 58 0.039
546
P PRN023 Prion Disease 57 0.039
547
AYM001 Ayme-Gripp Syndrome 57 0.039
548
PLS011 Plasmacytoma 56 0.039
549
P SZR006 Seizure Disorder 56 0.039
550
HMG005 Hemoglobinopathy 56 0.039
551
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.039
552
GST050 Gastrointestinal System Disease 56 0.039
553
PRP009 Peripartum Cardiomyopathy 55 0.039
554
HNC001 Henoch-Schoenlein Purpura 55 0.039
555
URN010 Urinary Tract Obstruction 55 0.039
556
PRC013 Pericarditis 54 0.039
557
CLL003 Cellulitis 54 0.039
558
c CNT016 Central Retinal Vein Occlusion 53 0.039
559
CRH005 Crohn's Colitis 53 0.039
560
P CNT005 Central Nervous System Lymphoma 53 0.039
561
HYP063 Hypersplenism 53 0.039
562
c XNT010 Xanthinuria, Type I 53 0.039
563
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.039
564
P RTN018 Retinal Disease 53 0.039
565
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
566
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.039
567
P DDN001 Duodenal Ulcer 52 0.039
568
CRT016 Carotid Artery Disease 52 0.039
569
NTR018 Neutrophilia, Hereditary 52 0.039
570
PLS009 Plasma Cell Neoplasm 51 0.039
571
INT079 Intrahepatic Cholangiocarcinoma 51 0.039
572
PPL021 Papilledema 49 0.039
573
c FLL041 Follicular Lymphoma 1 49 0.039
574
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.039
575
PTT004 Pituitary Apoplexy 48 0.039
576
LPT006 Leptin Receptor Deficiency 48 0.039
577
c PRM226 Primary Central Nervous System Lymphoma 48 0.039
578
PRL017 Prolymphocytic Leukemia 47 0.039
579
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.039
580
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.039
581
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.039
582
PLS025 Plasmablastic Lymphoma 47 0.039
583
c PRM093 Premature Ovarian Failure 7 47 0.039
584
NSS002 Neisseria Meningitidis Infection 47 0.039
585
RTN020 Retinal Vascular Disease 46 0.039
586
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.039
587
SMT001 Somatization Disorder 46 0.039
588
P HMR005 Hemorrhoid 46 0.039
589
ANR004 Anuria 46 0.039
590
P HRN001 Horner's Syndrome 45 0.039
591
MXD026 Mixed Glioma 45 0.039
592
c PCH010 Pachyonychia Congenita 3 44 0.039
593
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.039
594
HMP009 Haemophilus Influenzae 43 0.039
595
PNM013 Pneumococcal Meningitis 42 0.039
596
INT276 Interatrial Communication 42 0.039
597
RDN001 Reading Disorder 40 0.039
598
ASP030 Aspirin Resistance 39 0.039
599
P INT260 Intracranial Berry Aneurysm 39 0.039
600
TRN012 Transient Global Amnesia 39 0.039
601
PLC009 Placenta Praevia 39 0.039
602
DSS010 Dissociative Disorder 39 0.039
603
SCR011 Scrapie 39 0.039
604
c LKM005 Leukemia, T-Cell, Chronic 34 0.039
605
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.039
607
c PRS136 Prostate Cancer, Hereditary, 6 33 0.039
608
c PRS130 Prostate Cancer, Hereditary, 8 32 0.039
609
c THR102 Thrombocytopenia 5 30 0.039
610
RSP007 Respiratory Distress Syndrome, Infant 30 0.039
611
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.039
612
GNT005 Giant Hemangioma 28 0.039
613
GST019 Gastrointestinal Stromal Tumor 78 0.035
614
P PRK057 Parkinson Disease, Late-Onset 78 0.035
615
KPS004 Kaposi Sarcoma 75 0.035
616
c BTT014 Beta-Thalassemia 74 0.035
617
c MNN043 Meningioma, Familial 74 0.035
618
CRH001 Crohn's Disease 74 0.035
619
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.035
620
OTT002 Otitis Media 72 0.035
621
MYL009 Myelodysplastic Syndrome 70 0.035
622
P MYC084 Mycobacterium Tuberculosis 1 68 0.035
623
P DMN002 Dementia 66 0.035
624
P HYD006 Hydrocephalus 66 0.035
625
c MCL013 Mucolipidosis Iv 66 0.035
626
MSM014 Mismatch Repair Cancer Syndrome 65 0.035
627
OVR029 Ovarian Hyperstimulation Syndrome 64 0.035
628
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.035
629
c SYS004 Systemic Mastocytosis 63 0.035
630
ANR007 Anorexia Nervosa 63 0.035
631
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.035
632
MNN042 Meningioma, Radiation-Induced 62 0.035
633
MSS001 Masa Syndrome 62 0.035
634
YLL002 Yellow Fever 61 0.035
635
c WLM018 Wilms Tumor 5 61 0.035
636
ART141 Arteriovenous Malformations of the Brain 61 0.035
637
APP008 Appendicitis 61 0.035
638
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.035
639
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.035
640
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.035
641
P PTN014 Patent Ductus Arteriosus 1 60 0.035
642
ORL011 Oral Cancer 60 0.035
643
THY029 Thyroid Carcinoma 59 0.035
644
VSL002 Visual Epilepsy 59 0.035
645
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.035
646
P SYP003 Syphilis 58 0.035
647
P INT070 Intestinal Obstruction 58 0.035
648
P HYP726 Hypercalcemia, Infantile, 1 58 0.035
649
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.035
650
EYD002 Eye Disease 58 0.035
651
MNT002 Mental Depression 58 0.035
652
P PRP019 Peripheral Nervous System Disease 58 0.035
653
P ESP035 Esophagitis, Eosinophilic, 1 57 0.035
654
CHL067 Cholecystitis 57 0.035
655
P RHN004 Rhinitis 57 0.035
656
P FCL005 Focal Segmental Glomerulosclerosis 57 0.035
657
c ANG068 Angioedema, Hereditary, Type I 57 0.035
658
BLR008 Bilirubin Metabolic Disorder 57 0.035
659
JPN002 Japanese Encephalitis 57 0.035
660
P CHN012 Chondrosarcoma 56 0.035
661
HMT008 Hematuria, Benign Familial 56 0.035
662
EXF001 Exfoliation Syndrome 56 0.035
663
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.035
664
PRS047 Prostatitis 56 0.035
665
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.035
666
MTH009 Mouth Disease 56 0.035
667
ATR057 Atrioventricular Block 55 0.035
668
c PRG126 Progressive Familial Heart Block 55 0.035
669
VSC003 Visceral Leishmaniasis 55 0.035
670
P PLM034 Pulmonary Emphysema 55 0.035
671
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.035
672
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.035
673
GLC003 Glucose Intolerance 54 0.035
674
FCT003 Factor X Deficiency 54 0.035
675
AMN001 Amenorrhea 54 0.035
676
CLR030 Clear Cell Renal Cell Carcinoma 53 0.035
677
INT051 Intussusception 53 0.035
678
ACR041 Acromelic Frontonasal Dysostosis 52 0.035
679
PRS030 Persistent Fetal Circulation Syndrome 52 0.035
680
IMP005 Impotence 52 0.035
681
LMY002 Leiomyoma 52 0.035
682
FML026 Familial Lipoprotein Lipase Deficiency 51 0.035
683
P LCT001 Lactic Acidosis 51 0.035
684
PNN001 Panniculitis 51 0.035
685
PLR007 Pleural Empyema 50 0.035
686
SPN021 Spinal Meningioma 50 0.035
687
FSC004 Fasciitis 50 0.035
688
c THR071 Thrombocytopenia 1 50 0.035
689
ECT026 Ectopic Pregnancy 50 0.035
690
NTR046 Neutrophil Migration 50 0.035
691
DYS073 Dysphagia 50 0.035
692
LFT001 Left Bundle Branch Hemiblock 49 0.035
693
MCR004 Macroglobulinemia 49 0.035
694
GST049 Gastrointestinal System Cancer 49 0.035
695
HYP043 Hyperandrogenism 48 0.035
696
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.035
697
RGH001 Right Bundle Branch Block 48 0.035
698
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.035
699
c MLG069 Malignant Hypertension 47 0.035
700
P RNL015 Renal Hypertension 47 0.035
701
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 0.035
702
GST071 Gastrointestinal Carcinoma 47 0.035
703
CHR074 Choriocarcinoma 47 0.035
704
c ACT076 Acute Myocarditis 46 0.035
705
CLN045 Colonic Benign Neoplasm 46 0.035
706
KRT013 Keratolytic Winter Erythema 46 0.035
707
c DRR009 Diarrhea 6 46 0.035
708
CRT015 Carotid Artery Occlusion 45 0.035
709
c CLR017 Clear Cell Sarcoma 45 0.035
710
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.035
711
c CTR096 Cataract 6, Multiple Types 44 0.035
713
SBC016 Subacute Delirium 44 0.035
714
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.035
715
BNM001 Bone Marrow Cancer 43 0.035
716
SDD008 Sudden Sensorineural Hearing Loss 43 0.035
717
LWC001 Low Compliance Bladder 43 0.035
718
ANG011 Angiodysplasia 43 0.035
719
SCR001 Secretory Meningioma 41 0.035
720
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.035
721
CRN322 Coronavirus Infectious Disease 40 0.035
722
KDN007 Kidney Clear Cell Sarcoma 40 0.035
723
C1N001 C1 Inhibitor Deficiency 39 0.035
724
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.035
725
SPL006 Splenic Infarction 38 0.035
726
ALL014 Allergic Encephalomyelitis 38 0.035
727
c OVR114 Ovarian Cancer 1 38 0.035
728
LVD003 Livedoid Vasculitis 36 0.035
729
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.035
730
PLT015 Platelet Aggregation, Spontaneous 34 0.035
731
c CHR064 Chronic Monocytic Leukemia 33 0.035
732
BRN034 Brain Meningioma 33 0.035
733
INF013 Inferior Myocardial Infarction 33 0.035
734
DLF001 Dieulafoy Lesion 32 0.035
735
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.035
736
GNT019 Giant Cell Myocarditis 30 0.035
737
UND007 Undifferentiated Connective Tissue Disease 29 0.035
738
FML285 Familial Apolipoprotein C-Ii Deficiency 29 0.035
739
MLL004 Mallory-Weiss Syndrome 27 0.035
740
MSN003 Mesenteric Vascular Occlusion 27 0.035
741
ACT181 Acute Motor Axonal Neuropathy 26 0.035
742
JVN026 Jeavons Syndrome 24 0.035
743
INT053 Intracranial Vasospasm 24 0.035
744
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.030
745
P RTT002 Rett Syndrome 80 0.030
746
ANX010 Anxiety 73 0.030
747
c LKM063 Leukemia, Chronic Myeloid 72 0.030
748
ACR008 Acrocallosal Syndrome 69 0.030
749
SKN019 Skin Melanoma 68 0.030
750
P FRN006 Frontotemporal Dementia 68 0.030
751
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.030
752
ALL003 Allergic Rhinitis 67 0.030
753
LPT001 Leptospirosis 66 0.030
754
P CLC063 Celiac Disease 1 66 0.030
755
P SKN015 Skin Carcinoma 66 0.030
756
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.030
757
c WLM013 Wilms Tumor 1 65 0.030
758
TBC004 Tobacco Addiction 64 0.030
759
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.030
760
LYM017 Lyme Disease 64 0.030
761
P END044 Endometriosis 63 0.030
762
BLD131 Bladder Urothelial Carcinoma 62 0.030
763
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.030
764
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.030
765
HRP004 Herpes Zoster 60 0.030
766
PNM010 Pneumothorax, Primary Spontaneous 60 0.030
767
c LPM012 Lipomatosis, Multiple 60 0.030
768
P SCL018 Scoliosis 60 0.030
769
P TXP001 Toxoplasmosis 60 0.030
770
P CHR285 Chronic Myelomonocytic Leukemia 60 0.030
771
P LYM033 Lymphoproliferative Syndrome 59 0.030
772
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.030
773
GST045 Gastroenteritis 59 0.030
774
FBR047 Fibromyalgia 58 0.030
775
CRD132 Cardiac Conduction Defect 58 0.030
776
c DWL002 Dowling-Degos Disease 1 58 0.030
777
P GLL018 Gallbladder Cancer 57 0.030
778
BRN056 Bronchopulmonary Dysplasia 57 0.030
779
P MYM013 Moyamoya Disease 1 57 0.030
780
APH002 Aphasia 57 0.030
781
CYT008 Cytomegalovirus Infection 57 0.030
782
SCH014 Schistosomiasis 57 0.030
783
INT303 Intracranial Hypertension, Idiopathic 57 0.030
784
P ADL017 Adult T-Cell Leukemia 56 0.030
785
ERY051 Erythroleukemia, Familial 56 0.030
786
P PNM006 Pneumoconiosis 56 0.030
787
SLC006 Silicosis 56 0.030
788
P PLY019 Polyneuropathy 56 0.030
789
P PTT006 Pituitary Adenoma 55 0.030
790
CPL003 Capillary Leak Syndrome 55 0.030
791
ESN005 Eosinophilic Gastroenteritis 55 0.030
792
P DRM007 Dermatitis Herpetiformis 55 0.030
793
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.030
794
HRY003 Hairy Cell Leukemia 55 0.030
795
PYD001 Pyoderma Gangrenosum 54 0.030
796
GLS001 Gliosarcoma 54 0.030
797
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.030
798
TND005 Tendinitis 54 0.030
799
THR013 Thoracic Outlet Syndrome 54 0.030
800
LYM040 Lymphoblastic Lymphoma 54 0.030
801
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.030
802
NNL006 Non-Alcoholic Steatohepatitis 54 0.030
803
c HNT010 Huntington Disease-Like 1 53 0.030
804
P END047 Endophthalmitis 53 0.030
805
P EPD016 Epidermolysis Bullosa 53 0.030
806
c EXS019 Exostoses, Multiple, Type I 53 0.030
807
P PLM006 Pulmonary Alveolar Proteinosis 53 0.030
808
P SHR001 Short Bowel Syndrome 53 0.030
809
TXC002 Toxic Encephalopathy 53 0.030
810
P INT068 Intestinal Disease 53 0.030
811
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.030
812
P HYP730 Hypogonadotropic Hypogonadism 52 0.030
813
P MSC003 Muscular Atrophy 52 0.030
815
ILS001 Ileus 51 0.030
816
CLR109 Colorectal Adenocarcinoma 51 0.030
817
P AST007 Astrocytoma 51 0.030
818
c SCN007 Secondary Hyperparathyroidism 51 0.030
819
GNT002 Giant Cell Glioblastoma 50 0.030
820
PLR008 Pleurisy 50 0.030
821
NPH018 Nephrogenic Systemic Fibrosis 50 0.030
822
PYD002 Pyoderma 50 0.030
823
P OBS001 Obstructive Jaundice 50 0.030
824
HYP080 Hypogonadism 50 0.030
825
P ATR005 Atrophic Gastritis 50 0.030
826
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.030
827
PLP001 Pulpitis 49 0.030
828
P MST002 Mast-Cell Leukemia 49 0.030
829
NCR007 Necrotizing Fasciitis 48 0.030
830
P RNV001 Renovascular Hypertension 48 0.030
831
SPL018 Splenomegaly 48 0.030
832
P LYM024 Lymphatic System Disease 48 0.030
833
TBR011 Tuberculous Meningitis 48 0.030
834
ANT018 Anthracosis 48 0.030
835
CNT033 Central Nervous System Cancer 47 0.030
836
TST044 Testicular Torsion 47 0.030
837
AML029 Ameloblastoma 46 0.030
838
RTN023 Retinitis 46 0.030
839
GNR003 Generalized Atherosclerosis 46 0.030
840
DDN010 Duodenum Cancer 46 0.030
841
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.030
842
GST010 Gestational Trophoblastic Neoplasm 46 0.030
843
c ACT042 Acute Pyelonephritis 46 0.030
844
BNS007 Bone Sarcoma 45 0.030
845
c TRC022 Tricuspid Valve Insufficiency 45 0.030
846
INT253 Intestinal Benign Neoplasm 45 0.030
847
c NPH054 Nephrotic Syndrome, Type 3 45 0.030
848
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.030
849
c ACQ014 Acquired Hemophilia 45 0.030
850
GRN017 Granulocytopenia 44 0.030
851
c HYP272 Hypercholesterolemia, Familial, 3 44 0.030
852
FBR054 Fibroma 44 0.030
853
c SRC023 Sarcoidosis 2 43 0.030
854
P VND001 Vein Disease 42 0.030
855
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.030
856
SNL007 Senile Cataract 42 0.030
857
NRR001 Neuroretinitis 42 0.030
858
49X006 49, Xxxxy Syndrome 41 0.030
859
LRG008 Large Granular Lymphocyte Leukemia 41 0.030
860
KLD004 Keloid Disorder 40 0.030
861
P CRN074 Coronary Artery Aneurysm 39 0.030
862
c PLM022 Pulmonary Valve Insufficiency 39 0.030
863
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.030
864
c PLY105 Polycystic Ovary Syndrome 1 38 0.030
865
c SYS043 Systemic Lupus Erythematosus 1 38 0.030
866
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.030
867
MCP033 Mucopolysaccharidoses 38 0.030
868
c CHR098 Chronic Pyelonephritis 38 0.030
869
CRD016 Cardiac Rupture 37 0.030
870
c CHR020 Chronic Interstitial Cystitis 37 0.030
871
c WLM011 Wilms Tumor 6 37 0.030
872
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.030
873
WTR001 Waterhouse-Friderichsen Syndrome 36 0.030
874
ACT056 Acute Cor Pulmonale 36 0.030
875
PRN029 Parainfluenza Virus Type 3 36 0.030
876
c DRM040 Dermatitis Herpetiformis, Familial 35 0.030
877
LCH001 Leech Infestation 35 0.030
878
CHR178 Chromosomal Triplication 35 0.030
879
c MYM004 Moyamoya Disease 2 34 0.030
880
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.030
881
RFR002 Refractory Hairy Cell Leukemia 33 0.030
882
CVR002 Cavernous Sinus Thrombosis 33 0.030
883
CYT004 Cytomegalic Inclusion Disease 31 0.030
884
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.030
885
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.030
886
CLS052 Classic Hairy Cell Leukemia 27 0.030
887
CYT018 Cytochrome P450 2d6 Variant 27 0.030
888
MYT019 May-Thurner Syndrome 27 0.030
889
PLS031 Plastic Bronchitis 27 0.030
890
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.030
891
MSC026 Muscular Dystrophy White Matter Spongiosis 15 0.030
892
P ATX030 Ataxia-Telangiectasia 82 0.025
893
MRF001 Marfan Syndrome 77 0.025
894
CRV035 Cervical Cancer 76 0.025
895
c HMC039 Hemochromatosis, Type 1 74 0.025
896
P NJM001 Nijmegen Breakage Syndrome 74 0.025
897
VNH007 Von Hippel-Lindau Syndrome 73 0.025
898
c SPN225 Spondyloarthropathy 1 73 0.025
899
MSC157 Muscular Dystrophy, Duchenne Type 72 0.025
900
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.025
901
P MLT020 Multiple Sclerosis 72 0.025
902
SVR097 Severe Cutaneous Adverse Reaction 69 0.025
903
CRB037 Cerebral Palsy 69 0.025
904
P LPR021 Leprosy 3 69 0.025
905
EWN003 Ewing Sarcoma 69 0.025
906
P ANG001 Angelman Syndrome 69 0.025
907
PCK003 Pick Disease of Brain 68 0.025
908
P ALP004 Alport Syndrome 68 0.025
909
RCK004 Rickets 68 0.025
910
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.025
911
c PRM196 Premature Ovarian Failure 1 67 0.025
912
MYC006 Mycosis Fungoides 66 0.025
913
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 66 0.025
914
GLN010 Glanzmann Thrombasthenia 66 0.025
915
ART001 Arterial Tortuosity Syndrome 66 0.025
916
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.025
918
CHG001 Chagas Disease 66 0.025
919
P NRV007 Nervous System Disease 66 0.025
920
KHL003 Kohlschutter-Tonz Syndrome 65 0.025
921
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.025
922
PPL049 Papillon-Lefevre Syndrome 65 0.025
923
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.025
924
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.025
925
ANG020 Angiosarcoma 64 0.025
926
BRC012 Brucellosis 64 0.025
927
c MLG084 Malignant Fibrous Histiocytoma 63 0.025
928
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.025
929
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.025
930
P TRC086 Trichohepatoenteric Syndrome 1 62 0.025
931
BLL006 Bullous Pemphigoid 62 0.025
932
c ANM038 Anemia, Autoimmune Hemolytic 62 0.025
933
HSH003 Hashimoto Thyroiditis 62 0.025
934
MSL001 Measles 62 0.025
935
P DRM010 Dermatomyositis 61 0.025
937
c MCP043 Mucopolysaccharidosis, Type Iiia 61 0.025
938
CHR066 Chronic Fatigue Syndrome 61 0.025
939
WLD007 Waldenstroem's Macroglobulinemia 61 0.025
940
SZR001 Sezary's Disease 60 0.025
941
P TST021 Testicular Germ Cell Tumor 60 0.025
942
INT066 Interstitial Lung Disease 60 0.025
943
DNG002 Dengue Hemorrhagic Fever 60 0.025
944
STT001 Status Epilepticus 60 0.025
945
FCT002 Factor Xi Deficiency 60 0.025
946
PRT058 Pure Autonomic Failure 59 0.025
947
GNG013 Gingivitis 59 0.025
948
BRN002 Bronchiolitis 59 0.025
949
IRN001 Iron Deficiency Anemia 59 0.025
950
CHR072 Chordoma 58 0.025
951
ADR005 Adrenal Carcinoma 58 0.025
952
EXT034 Extrinsic Allergic Alveolitis 58 0.025
953
MXD005 Mixed Connective Tissue Disease 58 0.025
954
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.025
955
MCR013 Microphthalmia 57 0.025
956
c MST023 Mesothelioma, Malignant 57 0.025
957
APH001 Aphthous Stomatitis 57 0.025
958
PGM001 Pigmented Villonodular Synovitis 56 0.025
959
P BPL003 Bipolar Disorder 56 0.025
960
CMR002 Coumarin Resistance 56 0.025
961
ALL010 Allergic Contact Dermatitis 56 0.025
962
DBL002 Double Outlet Right Ventricle 56 0.025
963
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.025
964
P NRF002 Neurofibromatosis 56 0.025
965
ORL004 Oral Submucous Fibrosis 55 0.025
966
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.025
967
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.025
968
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
969
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.025
970
FCT004 Factor Xii Deficiency 55 0.025
971
P SLM003 Salmonellosis 55 0.025
972
SYN007 Synovitis 54 0.025
973
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.025
974
BRN014 Bronchopneumonia 54 0.025
975
P LTR001 Lateral Sclerosis 54 0.025
976
SNS003 Sensory Peripheral Neuropathy 54 0.025
977
PNC001 Pancytopenia 54 0.025
978
PST046 Post-Transplant Lymphoproliferative Disease 53 0.025
979
RHM028 Rheumatic Heart Disease 53 0.025
980
P RTN016 Retinal Degeneration 53 0.025
981
c PRD040 Periodontitis, Chronic 53 0.025
982
FNG017 Fungal Infectious Disease 53 0.025
983
P PTS002 Ptosis 53 0.025
984
DNT012 Dental Caries 53 0.025
985
P PNC025 Panic Disorder 53 0.025
986
c CNT035 Central Nervous System Disease 52 0.025
987
P THY032 Thyroiditis 52 0.025
988
ACT200 Acute Monoblastic Leukemia 52 0.025
989
c ACT135 Acute Graft Versus Host Disease 52 0.025
990
P TRT010 Teratoma 52 0.025
991
SPS003 Spastic Diplegia 51 0.025
992
MYL001 Myelitis 51 0.025
993
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.025
994
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.025
995
P CHL066 Cholangitis 51 0.025
996
URC002 Urea Cycle Disorder 51 0.025
997
RSP006 Respiratory System Disease 50 0.025
998
P SML016 Small Intestine Cancer 50 0.025
999
c EPL025 Epileptic Encephalopathy, Early Infantile, 2 50 0.025
1000
c HRD202 Hereditary Lymphedema I 50 0.025
1001
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.025
1002
HYP017 Hypophosphatemia 50 0.025
1003
PRT129 Prothrombin Deficiency, Congenital 50 0.025
1004
ATY042 Atypical Chronic Myeloid Leukemia 49 0.025
1005
c THR090 Thrombocythemia 1 49 0.025
1006
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.025
1007
P ART018 Aortic Valve Insufficiency 49 0.025
1008
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.025
1009
P END046 Endometritis 49 0.025
1010
SPT005 Spotted Fever 49 0.025
1011
QDR001 Quadriplegia 48 0.025
1012
ADR016 Adrenal Cortical Carcinoma 48 0.025
1013
RYN001 Raynaud Disease 48 0.025
1014
INT054 Intraocular Lymphoma 48 0.025
1015
CHR563 Chronic Eosinophilic Leukemia 48 0.025
1016
DBT006 Diabetic Macular Edema 48 0.025
1017
PNC013 Pancreatic Ductal Carcinoma 48 0.025
1018
c VRL012 Viral Meningitis 48 0.025
1019
ART004 Aortic Atherosclerosis 47 0.025
1020
P CRN028 Corneal Ulcer 47 0.025
1021
KRT008 Keratopathy 47 0.025
1022
P ERY008 Erythromelalgia 47 0.025
1023
LYM012 Lymphoplasmacytic Lymphoma 47 0.025
1024
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.025
1025
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.025
1026
ATN005 Autonomic Dysfunction 46 0.025
1027
MYC005 Myocardial Stunning 46 0.025
1028
MCR191 Microscopic Colitis 46 0.025
1029
PLL012 Pollen Allergy 46 0.025
1030
P LPC002 Lip Cancer 46 0.025
1031
P BNG032 Benign Mesothelioma 46 0.025
1032
P TRN034 Transverse Myelitis 45 0.025
1033
URT010 Ureteral Obstruction 45 0.025
1034
ORL013 Oral Lichen Planus 45 0.025
1035
PRL008 Paralytic Ileus 45 0.025
1036
P OCY003 Oocyte Maturation Defect 1 45 0.025
1037
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 45 0.025
1038
LYM051 Lymphomatoid Granulomatosis 45 0.025
1039
OVR112 Ovarian Germ Cell Cancer 45 0.025
1040
P CHR345 Chronic Pain 44 0.025
1041
CYS009 Cystadenoma 44 0.025
1042
CRD003 Cardiac Sarcoidosis 44 0.025
1043
CHL149 Childhood Acute Myeloid Leukemia 44 0.025
1044
PTT037 Pituitary Tumors 44 0.025
1045
IRT001 Iritis 44 0.025
1046
ART006 Arthus Reaction 44 0.025
1047
MST019 Mastoiditis 43 0.025
1048
P TST026 Testicular Germ Cell Cancer 43 0.025
1049
MYX004 Myxedema 43 0.025
1050
MCR011 Microinvasive Gastric Cancer 43 0.025
1051
P PLN008 Peeling Skin Syndrome 43 0.025
1052
HYP457 Hypertrophic Scars 42 0.025
1053
BNS003 Binswanger's Disease 42 0.025
1054
LPP002 Lipoprotein Glomerulopathy 42 0.025
1055
P PLM025 Pulmonary Venoocclusive Disease 42 0.025
1056
CHR286 Chronic Neutrophilic Leukemia 42 0.025
1057
c CHR576 Chronic Beryllium Disease 42 0.025
1058
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 42 0.025
1059
ANC002 Anca-Associated Vasculitis 41 0.025
1060
c RTN042 Retinitis Pigmentosa 12 41 0.025
1061
PRM013 Premature Menopause 41 0.025
1062
MTL005 Metal Allergy 41 0.025
1063
DFF003 Diffuse Scleroderma 41 0.025
1064
c MJR024 Major Affective Disorder 9 41 0.025
1065
ACT088 Acute Insulin Response 41 0.025
1066
MCL003 Macular Holes 40 0.025
1067
c HMG001 Hemoglobin C Disease 40 0.025
1068
BRY001 Berylliosis 40 0.025
1069
CLP006 Clopidogrel Resistance 40 0.025
1070
P BRY005 Beryllium Disease 40 0.025
1071
IMM001 Immune-Complex Glomerulonephritis 40 0.025
1072
UTR043 Uterine Sarcoma 39 0.025
1073
EXT006 Extrahepatic Cholestasis 39 0.025
1074
LKP003 Leukoplakia 39 0.025
1075
RCK002 Rocky Mountain Spotted Fever 39 0.025
1076
ADR004 Adrenal Cortical Adenocarcinoma 39 0.025
1077
ORL012 Oral Leukoplakia 39 0.025
1078
CHL070 Cholesterol Embolism 39 0.025
1079
FML039 Female Reproductive System Disease 39 0.025
1080
c HRD104 Hereditary Multiple Osteochondromas 39 0.025