Search results for Atorvastatin

769 hits were found for Atorvastatin

# Family MCID Name MIFTS Score
1
OBS306 Obsolete: Atorvastatin Toxicity 1 2.765
2
P OBS339 Obsolete: Susceptibility to Adverse Reaction Due to Atorvastatin Treatment 1 2.765
3
c HYP836 Hypercholesterolemia, Familial, 1 74 0.736
4
LPD008 Lipid Metabolism Disorder 64 0.579
5
ISC004 Ischemia 62 0.513
6
P CRN300 Coronary Heart Disease 1 59 0.513
7
P CRN018 Coronary Artery Anomaly 67 0.502
8
c HYP272 Hypercholesterolemia, Familial, 3 44 0.500
9
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.477
10
ART140 Arteries, Anomalies of 60 0.430
11
ATH013 Atherosclerosis Susceptibility 68 0.419
12
c FML035 Familial Hyperlipidemia 56 0.388
13
HYP081 Hypolipoproteinemia 51 0.373
14
P HRT032 Heart Disease 78 0.358
15
P MYC007 Myocardial Infarction 74 0.323
16
P DBT009 Diabetes Mellitus 66 0.310
17
CRB039 Cerebrovascular Disease 71 0.305
18
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.298
19
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.295
20
c HYP595 Hypertension, Essential 87 0.293
21
STR067 Stroke, Ischemic 82 0.292
22
P KDN018 Kidney Disease 73 0.284
23
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.267
24
c FML021 Familial Hypercholesterolemia 67 0.260
25
P VSC007 Vascular Disease 65 0.256
26
P MYP004 Myopathy 63 0.252
27
INT007 Intermediate Coronary Syndrome 58 0.234
28
ANG054 Angina Pectoris 66 0.230
29
c CHR684 Chronic Kidney Disease 68 0.227
30
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.225
31
P HYP750 Hypertriglyceridemia, Familial 62 0.213
32
c ACT075 Acute Myocardial Infarction 59 0.213
33
48X005 48,xyyy 37 0.207
34
CNG034 Congestive Heart Failure 69 0.200
35
P ATR011 Atrial Fibrillation 67 0.192
36
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.183
37
P LVR013 Liver Disease 71 0.179
38
ADL002 Adult Syndrome 62 0.171
39
FTT001 Fatty Liver Disease 63 0.169
40
PRP027 Peripheral Vascular Disease 72 0.167
41
OBS529 Obsolete: Combined Hyperlipidemia 22 0.167
42
THR024 Thrombosis 58 0.165
43
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.161
44
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.159
45
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.159
46
P PRD008 Periodontitis 66 0.157
47
c RHB024 Rhabdomyosarcoma 2 64 0.157
48
TRN015 Transient Cerebral Ischemia 62 0.157
49
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.157
50
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.157
51
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.153
52
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.151
53
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.151
54
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.151
55
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.151
56
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.151
57
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.151
58
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.151
59
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.151
60
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.151
61
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.151
62
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.148
63
P MLT020 Multiple Sclerosis 73 0.146
64
c FML001 Familial Atrial Fibrillation 67 0.144
65
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.144
66
c ACT071 Acute Kidney Failure 60 0.142
67
P ART021 Arteriosclerosis 56 0.139
68
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.139
69
c PRD040 Periodontitis, Chronic 56 0.137
70
c HYP740 Hyperlipoproteinemia, Type V 53 0.137
71
P PRS040 Prostate Cancer 97 0.134
72
c SYS001 Systemic Lupus Erythematosus 88 0.134
73
P TRN020 Turner Syndrome 66 0.134
74
P LPS004 Lupus Erythematosus 62 0.134
75
P RHM011 Rheumatoid Arthritis 82 0.129
76
HMN044 Human Immunodeficiency Virus Type 1 73 0.129
77
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.129
78
c ATR087 Atrial Standstill 1 76 0.127
79
P ART022 Arthritis 71 0.127
80
CYT002 Cytokine Deficiency 46 0.127
81
CRB004 Cerebral Artery Occlusion 38 0.127
82
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.124
83
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.124
84
P PLM037 Pulmonary Hypertension 69 0.121
85
NNL006 Non-Alcoholic Steatohepatitis 53 0.121
86
BNR002 Bone Resorption Disease 51 0.121
87
END030 End Stage Renal Failure 60 0.118
88
P MYS005 Myositis 54 0.118
89
P CRD119 Cardiac Arrest 71 0.116
90
ATM095 Autoimmune Disease 62 0.116
91
ANR040 Aneurysm 60 0.116
92
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.116
93
CRT013 Carotid Stenosis 50 0.116
94
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.116
95
c PRS136 Prostate Cancer, Hereditary, 6 34 0.116
96
c PRS130 Prostate Cancer, Hereditary, 8 33 0.116
97
P BRS047 Breast Cancer 99 0.113
98
DWN001 Down Syndrome 70 0.113
99
HYP066 Hyperglycemia 63 0.113
100
PRP080 Peripheral Artery Disease 51 0.113
101
ALL026 Allergic Hypersensitivity Disease 65 0.110
102
P PLY011 Polycystic Ovary Syndrome 58 0.110
103
c MCR113 Microvascular Complications of Diabetes 3 55 0.110
104
c MCR120 Microvascular Complications of Diabetes 7 48 0.110
105
c MCR130 Microvascular Complications of Diabetes 6 42 0.110
106
c MCR133 Microvascular Complications of Diabetes 4 42 0.110
107
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.110
108
P ALZ034 Alzheimer Disease 90 0.107
109
ACQ007 Acquired Immunodeficiency Syndrome 61 0.107
110
ALL014 Allergic Encephalomyelitis 40 0.107
111
CYT018 Cytochrome P450 2d6 Variant 28 0.107
112
P CLR023 Colorectal Cancer 100 0.103
113
ART016 Aortic Aneurysm 71 0.103
114
P HPT021 Hepatitis 69 0.103
115
P PSR002 Psoriasis 63 0.103
116
IMP005 Impotence 53 0.103
117
PST011 Pustulosis of Palm and Sole 51 0.103
118
P OST002 Osteoporosis 79 0.100
119
c THR092 Thrombophilia Due to Thrombin Defect 74 0.100
120
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.100
121
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.100
122
CRT016 Carotid Artery Disease 53 0.100
123
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.100
124
BRN071 Brain Injury 51 0.100
125
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.100
126
P GRF003 Graft-Versus-Host Disease 71 0.097
127
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.097
128
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.097
129
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.097
130
TRM010 Traumatic Brain Injury 54 0.097
131
LPD009 Lipid Storage Disease 49 0.097
132
IMM167 Immune Deficiency Disease 79 0.093
133
P LKM002 Leukemia 69 0.093
134
LVR012 Liver Cirrhosis 67 0.093
135
CHL068 Cholestasis 61 0.093
136
P PNC044 Pancreatitis 61 0.093
137
AGN016 Aging 58 0.093
138
FML235 Familial Combined Hyperlipoproteinemia 29 0.093
139
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.089
140
KWS002 Kawasaki Disease 65 0.089
141
HYP266 Hypoxia 58 0.089
142
HMC014 Homocysteinemia 54 0.089
143
c ACT135 Acute Graft Versus Host Disease 52 0.089
144
c DLT002 Dilated Cardiomyopathy 81 0.086
145
LPT014 Leptin Deficiency or Dysfunction 72 0.086
146
P LYM118 Lymphoma 70 0.086
147
P THR014 Thrombocytopenia 67 0.086
148
P PLM036 Pulmonary Fibrosis 66 0.086
149
IDP011 Idiopathic Interstitial Pneumonia 65 0.086
150
P END044 Endometriosis 63 0.086
151
SPN186 Spinal Cord Injury 63 0.086
152
RHM027 Rheumatic Disease 56 0.086
153
HYP005 Hypokalemia 55 0.086
154
HMT018 Hematopoietic Stem Cell Transplantation 54 0.086
155
GSG001 Gas Gangrene 52 0.086
156
CRN030 Coronary Stenosis 49 0.086
157
LYM019 Lymphosarcoma 48 0.086
158
ATX019 Ataxia with Vitamin E Deficiency 46 0.086
159
c PRM038 Primary Agammaglobulinemia 45 0.086
160
c HPT073 Hepatitis C Virus 74 0.082
161
c ART101 Aortic Valve Disease 2 67 0.082
162
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.082
163
c HPT001 Hepatitis C 62 0.082
164
P LYM031 Lymphocytic Leukemia 56 0.082
165
c PSR017 Psoriasis 2 55 0.082
166
c PSR023 Psoriasis 1 50 0.082
167
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.082
168
c PSR028 Psoriasis 7 40 0.082
169
c PSR018 Psoriasis 13 40 0.082
170
c PSR032 Psoriasis 11 40 0.082
171
GLB002 Glioblastoma 74 0.078
172
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.078
173
SCK003 Sickle Cell Anemia 74 0.078
174
P DMN002 Dementia 68 0.078
175
P MCR115 Microvascular Complications of Diabetes 5 67 0.078
176
P OCL013 Oculodentodigital Dysplasia 65 0.078
177
P NPH012 Nephrotic Syndrome 65 0.078
178
GLB015 Glioblastoma Multiforme 60 0.078
179
c ACT027 Acute Pancreatitis 60 0.078
180
c HPT003 Hepatitis a 60 0.078
181
PRM236 Primary Biliary Cholangitis 57 0.078
182
PRP030 Purpura 56 0.078
183
MSC190 Muscular Disease 54 0.078
184
OCL069 Ocular Motor Apraxia 53 0.078
185
P SCK005 Sickle Cell Disease 53 0.078
186
DYS014 Dyspepsia 51 0.078
187
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.078
188
P VSC018 Visceral Steatosis 34 0.078
189
HML018 Homologous Wasting Disease 22 0.078
190
c LKM061 Leukemia, Acute Myeloid 84 0.073
191
OST012 Osteoarthritis 80 0.073
192
P SLP006 Sleep Apnea 71 0.073
193
P LKM062 Leukemia, Acute Lymphoblastic 68 0.073
194
INC002 Inclusion Body Myositis 66 0.073
195
KHL003 Kohlschutter-Tonz Syndrome 63 0.073
196
LNG099 Lung Disease 62 0.073
197
P MYL006 Myeloid Leukemia 61 0.073
198
P CRD132 Cardiac Conduction Defect 61 0.073
199
P BRN022 Bronchiectasis 60 0.073
200
P MYC008 Myocarditis 60 0.073
201
P SZR006 Seizure Disorder 59 0.073
202
CNS004 Constipation 59 0.073
203
CMR002 Coumarin Resistance 56 0.073
204
HRT012 Heart Valve Disease 56 0.073
205
P PRM006 Primary Biliary Cirrhosis 54 0.073
206
P IDP024 Idiopathic Inflammatory Myopathy 49 0.073
207
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.073
208
c CHR064 Chronic Monocytic Leukemia 43 0.073
209
c SYS043 Systemic Lupus Erythematosus 1 39 0.073
210
P OVR096 Overlap Myositis 28 0.073
211
CHL079 Children's Interstitial Lung Disease 27 0.073
212
c ART115 Aortic Valve Disease 1 76 0.068
213
SVR004 Severe Combined Immunodeficiency 74 0.068
214
P PNM007 Pneumonia 71 0.068
215
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.068
216
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.068
217
P ADN016 Adenocarcinoma 65 0.068
218
APN008 Apnea, Obstructive Sleep 64 0.068
219
PRT013 Portal Hypertension 61 0.068
220
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.068
221
MNT002 Mental Depression 60 0.068
222
PLM033 Pulmonary Embolism 60 0.068
223
P EXN002 Exanthem 58 0.068
224
P PLY041 Polymyositis 57 0.068
225
P DRR001 Diarrhea 55 0.068
226
P INS002 in Situ Carcinoma 55 0.068
227
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.068
228
LYM040 Lymphoblastic Lymphoma 54 0.068
229
47X002 47,xyy 49 0.068
230
P BLD051 Blood Coagulation Disease 48 0.068
231
P CRN074 Coronary Artery Aneurysm 47 0.068
232
DST006 Diastolic Heart Failure 43 0.068
233
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.068
234
CLP006 Clopidogrel Resistance 41 0.068
235
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.068
236
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.068
237
P PNC035 Pancreatic Cancer 86 0.063
238
MYL069 Myeloma, Multiple 85 0.063
239
CRH001 Crohn's Disease 75 0.063
240
P HYP086 Hypothyroidism 70 0.063
241
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.063
242
c MCR129 Microvascular Complications of Diabetes 1 67 0.063
243
MSC007 Muscle Hypertrophy 65 0.063
244
P DRM010 Dermatomyositis 62 0.063
245
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.063
246
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.063
247
P NRP001 Neuropathy 57 0.063
248
HYP060 Hyperinsulinism 55 0.063
249
GLC003 Glucose Intolerance 55 0.063
250
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.063
251
DMY004 Demyelinating Disease 54 0.063
252
c HYP739 Hyperlipoproteinemia, Type Iv 50 0.063
253
PRD004 Prediabetes Syndrome 49 0.063
254
GLL048 Glial Tumor 48 0.063
255
c HNT004 Huntington Disease-Like 2 48 0.063
256
BHR001 Behr Syndrome 47 0.063
257
URT010 Ureteral Obstruction 46 0.063
258
c PCH010 Pachyonychia Congenita 3 43 0.063
259
c MCR112 Microvascular Complications of Diabetes 2 42 0.063
260
c PLY105 Polycystic Ovary Syndrome 1 38 0.063
261
c HNT011 Huntington Disease-Like 3 37 0.063
262
CYS001 Cystic Fibrosis 84 0.058
263
AST005 Asthma 80 0.058
264
DFC004 Deficiency Anemia 77 0.058
265
P EPL164 Epilepsy 73 0.058
266
P TBR001 Tuberous Sclerosis 72 0.058
267
MYL009 Myelodysplastic Syndrome 72 0.058
268
BRN024 Bronchitis 70 0.058
269
LYM133 Lymphoma, Hodgkin, Classic 70 0.058
270
HYP056 Hypoglycemia 68 0.058
271
SKN019 Skin Melanoma 68 0.058
272
MLN008 Melanoma 68 0.058
273
P HYP098 Hypereosinophilic Syndrome 67 0.058
274
DPR016 Depression 64 0.058
275
P VSC011 Vasculitis 64 0.058
276
c FNC043 Fanconi Anemia, Complementation Group E 64 0.058
277
P GLM045 Glioma 64 0.058
278
c ATM011 Autoimmune Hepatitis 63 0.058
279
CLT003 Colitis 63 0.058
280
BRS099 Breast Ductal Carcinoma 63 0.058
281
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.058
282
c SCL052 Scleroderma, Familial Progressive 62 0.058
283
P CTR002 Cataract 62 0.058
284
P BCL017 B-Cell Lymphoma 61 0.058
285
NTR005 Nutritional Deficiency Disease 61 0.058
286
P HDC001 Headache 59 0.058
287
P GLM007 Glomerulonephritis 58 0.058
288
IRN002 Iron Metabolism Disease 58 0.058
289
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.058
290
BRN004 Brain Edema 57 0.058
291
c VRL010 Viral Hepatitis 56 0.058
292
P CHL066 Cholangitis 53 0.058
293
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.058
294
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.058
295
c LTN004 Late-Onset Retinal Degeneration 49 0.058
296
HYP043 Hyperandrogenism 48 0.058
297
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.058
298
HDN002 Head Injury 47 0.058
299
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.058
300
KRT013 Keratolytic Winter Erythema 45 0.058
301
SYS003 Systolic Heart Failure 43 0.058
302
TRP009 Triple X Syndrome 42 0.058
303
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.058
304
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.058
305
c HYP163 Hyperlipidemia Type 3 23 0.058
306
P HPT023 Hepatocellular Carcinoma 99 0.052
307
P OVR042 Ovarian Cancer 89 0.052
308
c LKM071 Leukemia, Chronic Lymphocytic 81 0.052
309
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.052
310
P BLD134 Bladder Cancer 79 0.052
311
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.052
312
c TBR025 Tuberous Sclerosis 1 74 0.052
313
P SRC025 Sarcoidosis 1 72 0.052
314
P SYS005 Systemic Scleroderma 68 0.052
315
P HYP061 Hypertrophic Cardiomyopathy 68 0.052
316
ALC007 Alcohol Dependence 68 0.052
317
PRT036 Peritonitis 66 0.052
318
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.052
319
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.052
320
SKN016 Skin Disease 64 0.052
321
c HPT016 Hepatitis B 63 0.052
322
GT001 Gout 63 0.052
323
c PRC016 Pre-Eclampsia 63 0.052
324
P HMN010 Hemangioma 62 0.052
325
P INT143 Interstitial Cystitis 62 0.052
326
c PNS012 Paine Syndrome 61 0.052
327
P URT039 Urticaria 61 0.052
328
INT002 Intermittent Claudication 60 0.052
329
P BPL003 Bipolar Disorder 59 0.052
330
P ALC033 Alcohol Use Disorder 58 0.052
331
VSC002 Vascular Dementia 57 0.052
332
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.052
333
PLM010 Pulmonary Edema 56 0.052
334
P DBT005 Diabetes Insipidus 54 0.052
335
P ECL001 Eclampsia 53 0.052
336
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.052
337
RYN005 Raynaud Phenomenon 50 0.052
338
c PRM108 Primary Progressive Multiple Sclerosis 49 0.052
339
RNL077 Renal Fibrosis 49 0.052
340
CLC006 Calcinosis 48 0.052
341
HYP025 Hyperphosphatemia 47 0.052
342
CRB008 Cerebral Atherosclerosis 47 0.052
343
ENT004 Enthesopathy 46 0.052
344
ART031 Aortic Coarctation 45 0.052
345
CRN017 Coronary Thrombosis 45 0.052
346
P MYG005 Myoglobinuria 43 0.052
347
P PRC031 Preeclampsia/eclampsia 1 42 0.052
348
ASP030 Aspirin Resistance 42 0.052
349
c MJR024 Major Affective Disorder 9 42 0.052
350
P GLM044 Glomerular Disease 42 0.052
351
ADS004 Aids Dementia Complex 41 0.052
352
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.052
353
c HMG029 Hemoglobin Se Disease 40 0.052
354
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.052
355
49X002 49,xxxxy Syndrome 39 0.052
356
SPR126 Superior Semicircular Canal Dehiscence 39 0.052
357
c MJR022 Major Affective Disorder 8 39 0.052
358
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 34 0.052
359
c MYC058 Myocardial Infarction 2 30 0.052
360
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.052
361
INT074 Intracranial Arteriosclerosis 17 0.052
362
STT044 Statin Toxicity 12 0.052
363
P LNG032 Lung Cancer 99 0.045
364
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.045
365
CNN003 Conn's Syndrome 78 0.045
366
P RSP003 Respiratory Failure 75 0.045
367
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.045
368
END057 Endometrial Cancer 74 0.045
369
c SPN225 Spondyloarthropathy 1 74 0.045
370
ADR007 Adrenoleukodystrophy 72 0.045
371
RCK004 Rickets 70 0.045
372
c PNC108 Pancreatitis, Hereditary 70 0.045
373
P MYS003 Myasthenia Gravis 68 0.045
374
WRN001 Werner Syndrome 68 0.045
375
P GLM040 Glioma Susceptibility 1 68 0.045
376
P NSP012 Nasopharyngeal Carcinoma 67 0.045
377
LYM007 Lymphangioleiomyomatosis 67 0.045
378
P CNJ013 Conjunctivitis 67 0.045
379
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.045
380
P SKN015 Skin Carcinoma 67 0.045
381
c INF071 Inflammatory Bowel Disease 1 66 0.045
382
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.045
383
P CRB048 Cerebral Cavernous Malformations 65 0.045
384
c GCH015 Gaucher Disease, Type I 65 0.045
385
CLN015 Colon Adenocarcinoma 65 0.045
386
P ENC018 Encephalopathy 64 0.045
387
P GCH001 Gaucher's Disease 63 0.045
388
PSR001 Psoriatic Arthritis 63 0.045
389
PCK003 Pick Disease of Brain 63 0.045
390
TXC005 Toxic Shock Syndrome 63 0.045
391
P FCL005 Focal Segmental Glomerulosclerosis 63 0.045
392
P SNS001 Sensorineural Hearing Loss 62 0.045
393
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.045
394
CRD223 Cardiac Arrhythmia 61 0.045
395
STT001 Status Epilepticus 61 0.045
396
c LCL006 Localized Scleroderma 61 0.045
397
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.045
398
P NMN002 Niemann-Pick Disease 60 0.045
399
ALC006 Alcoholic Hepatitis 60 0.045
400
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.045
401
P KDN017 Kidney Cancer 60 0.045
402
HPT019 Hepatic Encephalopathy 60 0.045
403
HMR039 Hemorrhage, Intracerebral 59 0.045
404
EYD002 Eye Disease 59 0.045
405
P BRS044 Breast Adenocarcinoma 59 0.045
406
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.045
407
VSL002 Visual Epilepsy 58 0.045
408
P PRP029 Porphyria 58 0.045
409
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.045
410
P ALP008 Alopecia 58 0.045
411
P SLP005 Sleep Disorder 58 0.045
412
P INF037 Inflammatory Bowel Disease 57 0.045
413
DCT002 Ductal Carcinoma in Situ 57 0.045
414
P GRV001 Graves' Disease 57 0.045
415
APH002 Aphasia 56 0.045
416
ALL006 Allergic Asthma 56 0.045
417
CRH005 Crohn's Colitis 56 0.045
418
c CHR417 Chronic Graft Versus Host Disease 56 0.045
419
P SBS003 Substance Abuse 56 0.045
420
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.045
421
AMN003 Amnestic Disorder 55 0.045
422
P HYP076 Hyperthyroidism 55 0.045
423
P PLY019 Polyneuropathy 55 0.045
424
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.045
425
PLM012 Pulmonary Sarcoidosis 54 0.045
426
P HYP730 Hypogonadotropic Hypogonadism 54 0.045
427
PRC013 Pericarditis 54 0.045
428
HYP014 Hyperuricemia 52 0.045
429
P CPL006 Capillary Hemangioma 52 0.045
430
NRT004 Neuritis 52 0.045
431
MCL006 Macular Retinal Edema 52 0.045
432
c INF023 Inflammatory Breast Carcinoma 52 0.045
433
c BRS049 Breast Carcinoma in Situ 51 0.045
434
IMM064 Immunodeficiency, Common Variable, 10 51 0.045
435
BLD053 Blood Platelet Disease 51 0.045
436
P RTN022 Retinal Vein Occlusion 50 0.045
437
SCH012 Schizoaffective Disorder 50 0.045
438
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.045
439
ACR041 Acromelic Frontonasal Dysostosis 50 0.045
440
IGG001 Iga Glomerulonephritis 50 0.045
441
c INF145 Infantile Liver Failure Syndrome 1 50 0.045
442
HYP006 Hypertensive Heart Disease 49 0.045
443
c MTR002 Mitral Valve Insufficiency 49 0.045
444
P RNV001 Renovascular Hypertension 49 0.045
445
c ACT078 Acute Porphyria 49 0.045
446
CVR006 Cavernous Hemangioma 49 0.045
447
c CNT016 Central Retinal Vein Occlusion 48 0.045
448
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.045
449
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.045
450
c HYP837 Hypercholesterolemia, Familial, 2 48 0.045
451
RYN001 Raynaud Disease 48 0.045
452
ACT017 Acute Chest Syndrome 47 0.045
453
CRB027 Cerebellar Disease 47 0.045
454
NPH010 Nephrosclerosis 46 0.045
455
MYC005 Myocardial Stunning 45 0.045
456
BCK006 Back Pain 44 0.045
457
P MJR007 Major Affective Disorder 1 44 0.045
458
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.045
459
ATN004 Autonomic Neuropathy 43 0.045
460
c SRC023 Sarcoidosis 2 43 0.045
461
DFF003 Diffuse Scleroderma 43 0.045
462
P AVS003 Avascular Necrosis 43 0.045
463
MMM006 Mammographic Density 43 0.045
464
HPT004 Hepatic Coma 42 0.045
465
RTR011 Retroperitoneal Fibrosis 41 0.045
466
NSP002 Nasopharyngitis 41 0.045
468
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 37 0.045
469
FBR089 Fibrosclerosis, Multifocal 37 0.045
470
c ATM022 Autoimmune Myocarditis 36 0.045
471
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 36 0.045
472
47X003 47, Xxy 36 0.045
473
CVR010 Cavernous Malformation 36 0.045
474
c MJR008 Major Affective Disorder 2 35 0.045
475
CRN006 Coronary Aneurysm 35 0.045
476
ACT011 Acute Contagious Conjunctivitis 35 0.045
477
c MJR003 Major Affective Disorder 6 34 0.045
478
c MJR006 Major Affective Disorder 5 34 0.045
479
c MJR023 Major Affective Disorder 7 34 0.045
480
CRB031 Cerebral Arterial Disease 30 0.045
481
c MJR004 Major Affective Disorder 4 29 0.045
482
PRQ002 Paraquat Poisoning 25 0.045
483
ACR039 Acromegaloid Hypertrichosis Syndrome 25 0.045
484
CNT023 Central Nervous System Hemangioma 13 0.045
485
MLR004 Malaria 82 0.037
486
P RTN024 Retinoblastoma 74 0.037
487
c LKM063 Leukemia, Chronic Myeloid 74 0.037
488
P CNR004 Cone-Rod Dystrophy 2 72 0.037
489
c MGR028 Migraine with or Without Aura 1 70 0.037
490
MNT001 Mantle Cell Lymphoma 69 0.037
491
P MYC084 Mycobacterium Tuberculosis 1 69 0.037
492
P INF038 Influenza 69 0.037
493
P MJR001 Major Depressive Disorder 69 0.037
494
OBS002 Obsessive-Compulsive Disorder 69 0.037
495
CHL065 Cholangiocarcinoma 68 0.037
496
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.037
497
SRC014 Sarcoma 67 0.037
498
CHG001 Chagas Disease 66 0.037
499
MYL031 Myeloproliferative Neoplasm 66 0.037
500
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.037
501
MSM014 Mismatch Repair Cancer Syndrome 65 0.037
502
CLR108 Colorectal Adenoma 64 0.037
503
TNG002 Tangier Disease 64 0.037
504
P HYP069 Hyperparathyroidism 64 0.037
505
P VNW001 Von Willebrand's Disease 64 0.037
506
HMT002 Hematologic Cancer 64 0.037
507
P NTR004 Neutropenia 64 0.037
508
DRM006 Dermatitis 63 0.037
509
HYP020 Hyperprolactinemia 62 0.037
510
OST003 Osteonecrosis 62 0.037
511
LYM012 Lymphoplasmacytic Lymphoma 62 0.037
512
VRL011 Viral Infectious Disease 62 0.037
513
IGR001 Ige Responsiveness, Atopic 61 0.037
514
PPT005 Peptic Ulcer Disease 60 0.037
515
PST028 Post-Traumatic Stress Disorder 60 0.037
516
c ACT210 Acute Respiratory Distress Syndrome 59 0.037
517
P MTR012 Mitral Valve Disease 59 0.037
518
P MTC069 Mitochondrial Disorders 57 0.037
519
BCT022 Bacterial Infectious Disease 57 0.037
520
SFT003 Soft Tissue Sarcoma 57 0.037
521
SPN035 Spindle Cell Sarcoma 57 0.037
522
DBT010 Diabetic Neuropathy 56 0.037
523
SYN007 Synovitis 55 0.037
524
BRD001 Brody Myopathy 55 0.037
525
INT079 Intrahepatic Cholangiocarcinoma 54 0.037
526
PTT009 Pituitary Gland Disease 54 0.037
527
PRP016 Paraplegia 54 0.037
528
P RCT021 Rectum Cancer 54 0.037
529
P HYP083 Hypopituitarism 53 0.037
530
P TMP001 Temporal Lobe Epilepsy 53 0.037
531
LNG031 Lung Benign Neoplasm 52 0.037
532
P THY032 Thyroiditis 52 0.037
533
c SCN007 Secondary Hyperparathyroidism 52 0.037
534
P ANL018 Analbuminemia 51 0.037
535
GLS018 Glass Syndrome 51 0.037
536
HYP080 Hypogonadism 51 0.037
537
P PST095 Post-Thrombotic Syndrome 50 0.037
538
MTC005 Mitochondrial Metabolism Disease 50 0.037
539
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.037
540
MCR004 Macroglobulinemia 50 0.037
541
CRD137 Cardiogenic Shock 50 0.037
542
c HYP768 Hyperlipoproteinemia, Type I 50 0.037
543
c MLG074 Malignant Mesenchymoma 50 0.037
544
SXL003 Sexual Disorder 49 0.037
545
HPT009 Hepatopulmonary Syndrome 49 0.037
546
ATS010 Autosomal Recessive Disease 49 0.037
547
GYN001 Gynecomastia 49 0.037
548
HPT014 Hepatorenal Syndrome 49 0.037
549
HYP781 Hypoascorbemia 48 0.037
550
EBL001 Ebola Hemorrhagic Fever 48 0.037
551
BNM001 Bone Marrow Cancer 48 0.037
552
CRN019 Coronary Artery Vasospasm 48 0.037
553
ADR038 Adermatoglyphia 48 0.037
554
WTH001 Withdrawal Disorder 47 0.037
555
LPT006 Leptin Receptor Deficiency 47 0.037
556
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.037
557
ART004 Aortic Atherosclerosis 47 0.037
558
DBT006 Diabetic Macular Edema 46 0.037
559
c FML008 Familial Retinoblastoma 46 0.037
560
P CLL015 Collagen Disease 46 0.037
561
SYN036 Syncope 46 0.037
562
PRL017 Prolymphocytic Leukemia 45 0.037
563
ANG011 Angiodysplasia 45 0.037
564
TND005 Tendinitis 45 0.037
565
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.037
566
OBS082 Obstructive Nephropathy 44 0.037
567
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 44 0.037
568
TND004 Tendinopathy 44 0.037
569
DRG024 Drug Allergy 43 0.037
570
SBC016 Subacute Delirium 43 0.037
571
ACT084 Acute Stress Disorder 42 0.037
572
GST020 Gastric Antral Vascular Ectasia 42 0.037
573
RDN001 Reading Disorder 42 0.037
574
HYP540 Hypertension, Diastolic 41 0.037
575
PLS016 Plasma Cell Leukemia 41 0.037
576
CRB086 Cerebral Aneurysms 41 0.037
577
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.037
578
HYP064 Hypogonadotropism 40 0.037
579
c OVR114 Ovarian Cancer 1 39 0.037
580
ANT039 Antisynthetase Syndrome 39 0.037
581
P INT260 Intracranial Berry Aneurysm 38 0.037
582
c LKM004 Leukemia, B-Cell, Chronic 35 0.037
583
RNL001 Renal Artery Obstruction 33 0.037
584
INF021 Infant Gynecomastia 32 0.037
585
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 31 0.037
586
INF118 Inflammatory Myopathy with Abundant Macrophages 29 0.037
587
c HYP843 Hypoalphalipoproteinemia, Primary, 2 29 0.037
588
KDN013 Kidney Hypertrophy 27 0.037
589
HDG004 Hodgkin's Granuloma 27 0.037
590
c CLB022 Coloboma, Ocular, Autosomal Recessive 27 0.037
591
FTL073 Fetal Anticonvulsant Syndrome 26 0.037
592
SCN001 Secondary Hyperparathyroidism of Renal Origin 23 0.037
593
HDG006 Hodgkin's Paragranuloma 23 0.037
594
c CNG336 Congenital Analbuminemia 19 0.037
595
ESP021 Esophageal Cancer 90 0.026
596
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.026
598
c FNC027 Fanconi Anemia, Complementation Group a 81 0.026
599
P NRF023 Neurofibromatosis, Type Ii 77 0.026
600
ULC004 Ulcerative Colitis 75 0.026
601
BRN028 Brain Cancer 75 0.026
602
ANX010 Anxiety 75 0.026
603
P FML011 Familial Adenomatous Polyposis 73 0.026
604
P AMY004 Amyloidosis 71 0.026
605
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.026
606
ACR007 Acromegaly 70 0.026
607
P HYD006 Hydrocephalus 68 0.026
608
GST092 Gastroesophageal Reflux 68 0.026
609
CNN005 Connective Tissue Disease 68 0.026
610
c HRD010 Hereditary Spastic Paraplegia 67 0.026
611
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 67 0.026
612
P PSD087 Pseudoxanthoma Elasticum 67 0.026
613
OST159 Osteogenic Sarcoma 67 0.026
614
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.026
615
P NRB010 Neuroblastoma 1 66 0.026
616
OST017 Osteomyelitis 65 0.026
617
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.026
618
KRN002 Kearns-Sayre Syndrome 64 0.026
619
c GLC092 Glaucoma, Primary Open Angle 63 0.026
620
c BRN108 Branchiootic Syndrome 1 62 0.026
621
TTN003 Tetanus 62 0.026
622
INT066 Interstitial Lung Disease 61 0.026
623
P ART023 Arthropathy 61 0.026
624
HLC007 Helicobacter Pylori Infection 61 0.026
625
SPP011 Suppression of Tumorigenicity 12 61 0.026
626
SQM006 Squamous Cell Carcinoma 60 0.026
627
CHL067 Cholecystitis 60 0.026
628
BRN002 Bronchiolitis 60 0.026
629
ADN018 Adenoma 60 0.026
630
P INT070 Intestinal Obstruction 60 0.026
631
P INF032 Infertility 60 0.026
632
P CYS018 Cystitis 59 0.026
633
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 59 0.026
634
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.026
635
P UVT001 Uveitis 58 0.026
636
CYT008 Cytomegalovirus Infection 58 0.026
637
GST033 Gestational Diabetes 58 0.026
638
HYD002 Hydronephrosis 58 0.026
639
CHL014 Cholera 58 0.026
640
HPT022 Hepatoblastoma 58 0.026
641
P GST044 Gastritis 58 0.026
642
SCH014 Schistosomiasis 57 0.026
643
TRN018 Transitional Cell Carcinoma 57 0.026
644
P MLN007 Male Infertility 57 0.026
645
INT030 Intracranial Aneurysm 57 0.026
646
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 57 0.026
647
P GLL022 Guillain-Barre Syndrome 56 0.026
648
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 56 0.026
649
ATR057 Atrioventricular Block 56 0.026
650
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.026
651
MCS002 Mucositis 56 0.026
652
P PMP001 Pemphigus 56 0.026
653
P LTR001 Lateral Sclerosis 56 0.026
654
GRN034 Grange Syndrome 55 0.026
655
c CNG216 Congenital Hydrocephalus 55 0.026
656
P PLM034 Pulmonary Emphysema 55 0.026
657
BRN012 Bronchiolitis Obliterans 55 0.026
658
ESP023 Esophageal Disease 55 0.026
659
P LCH002 Lichen Planus 55 0.026
660
c GRV008 Graves Disease 1 55 0.026
661
SPT004 Septic Arthritis 55 0.026
662
PRS045 Prostatic Hypertrophy 55 0.026
663
DCB001 Decubitus Ulcer 54 0.026
664
PLG002 Plague 54 0.026
665
INT075 Intracranial Hypertension 54 0.026
666
PLS007 Plasmodium Falciparum Malaria 53 0.026
667
TLN003 Telangiectasis 53 0.026
668
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.026
669
P MYS079 Miyoshi Muscular Dystrophy 53 0.026
670
c GLL024 Gallbladder Disease 1 53 0.026
671
c ACT134 Acute Liver Failure 53 0.026
672
GST023 Gastric Ulcer 53 0.026
673
LMY002 Leiomyoma 52 0.026
674
P MNC007 Monocytic Leukemia 52 0.026
675
PRS021 Prostatic Adenoma 52 0.026
676
P TRT010 Teratoma 52 0.026
677
CRY005 Cryptococcosis 51 0.026
678
OVR082 Overgrowth Syndrome 51 0.026
679
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.026
680
QDR001 Quadriplegia 51 0.026
681
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.026
682
CRY003 Cryptosporidiosis 50 0.026
683
P IGN003 Iga Nephropathy 1 50 0.026
684
P OPN001 Open-Angle Glaucoma 50 0.026
685
PLR008 Pleurisy 50 0.026
686
MNN009 Meningoencephalitis 50 0.026
687
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.026
688
PRS129 Prostatic Hyperplasia, Benign 49 0.026
689
RTN020 Retinal Vascular Disease 49 0.026
690
c BCT013 Bacterial Pneumonia 49 0.026
691
THR013 Thoracic Outlet Syndrome 49 0.026
692
MTB004 Metabolic Acidosis 48 0.026
693
BLP005 Blepharitis 48 0.026
694
ATN005 Autonomic Dysfunction 48 0.026
695
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.026
696
DBT004 Diabetic Polyneuropathy 48 0.026
697
ESN015 Eosinophilic Fasciitis 48 0.026
698
HDR003 Hidradenitis 48 0.026
699
P HMR005 Hemorrhoid 47 0.026
700
INT010 Intracranial Embolism 47 0.026
701
HPT025 Hepatic Lipase Deficiency 47 0.026
702
P MYC033 Myoclonus 47 0.026
703
FSC004 Fasciitis 47 0.026
704
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.026
705
MCR037 Macroglossia 46 0.026
706
HLX001 Helix Syndrome 46 0.026
707
c RCR022 Recurrent Acute Pancreatitis 46 0.026
708
ASP007 Aspiration Pneumonia 46 0.026
709
P CMP008 Compartment Syndrome 45 0.026
710
c ATM099 Autoimmune Uveitis 45 0.026
711
c DYS119 Dystonia 9 45 0.026
712
RTR008 Root Resorption 44 0.026
713
ORL015 Oral Squamous Cell Carcinoma 44 0.026
714
PLY068 Polysubstance Abuse 44 0.026
715
ANX004 Anoxia 44 0.026
716
CRT015 Carotid Artery Occlusion 44 0.026
717
INT052 Intestinal Volvulus 44 0.026
718
ANC002 Anca-Associated Vasculitis 43 0.026
719
PRS115 Prosthetic Joint Infection 43 0.026
720
P CRB088 Cerebral Atrophy 43 0.026
721
CYS009 Cystadenoma 43 0.026
722
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.026
723
CRS001 Crescentic Glomerulonephritis 42 0.026
724
ALC010 Alcoholic Cardiomyopathy 42 0.026
725
TND006 Tendinosis 42 0.026
726
P CRC039 Coarctation of Aorta 42 0.026
727
CHR466 Chronic Thromboembolic Pulmonary Hypertension 41 0.026
728
P SBR004 Seborrheic Dermatitis 41 0.026
729
DRG002 Drug-Induced Hepatitis 41 0.026
730
MYF001 Myofibroma 40 0.026
731
c CHR096 Chronic Pulmonary Heart Disease 40 0.026
732
LNR006 Linear Iga Disease 40 0.026
733
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.026
734
HMR023 Hemorrhagic Cystitis 40 0.026
735
PLT015 Platelet Aggregation, Spontaneous 40 0.026
736
THR099 Third-Degree Atrioventricular Block 39 0.026
737
EXT006 Extrahepatic Cholestasis 38 0.026
738
SPS057 Spasticity 38 0.026
739
HRN029 Hearing Loss, Noise-Induced 38 0.026
740
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 38 0.026
741
RTR001 Retrograde Amnesia 38 0.026
742
BCK003 Background Diabetic Retinopathy 37 0.026
743
P ANT001 Anterolateral Myocardial Infarction 37 0.026
744
AMR003 Amaurosis Fugax 36 0.026
745
c PRG020 Paragangliomas 3 36 0.026
746
FXD003 Fixed Drug Eruption 36 0.026
747
c CHR682 Chronic Bilirubin Encephalopathy 36 0.026
748
HMM004 Hamamy Syndrome 36 0.026
749
SBC014 Subclavian Steal Syndrome 36 0.026
751
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.026
752
MNN002 Mononeuritis Multiplex 33 0.026
753
LCH013 Lichen Planus Pemphigoides 33 0.026
754
RRS014 Rare Surgical Neurologic Disease 33 0.026
755
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.026
756
ART012 Aortitis 33 0.026
757
ART010 Arteriolosclerosis 32 0.026
758
c SPS036 Spastic Paraplegia 3 31 0.026
759
PMP009 Pemphigus Erythematosus 29 0.026
760
c HRD138 Hereditary Motor and Sensory Neuropathy V 29 0.026
761
SLR005 Solar Urticaria 29 0.026
762
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.026
763
PTN004 Patent Ductus Venosus 26 0.026
764
NCR015 Necrotizing Autoimmune Myopathy 26 0.026
765
P CRT085 Carotid Intimal Medial Thickness 2 25 0.026
766
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.026
767
TLM001 Telomere Length, Mean Leukocyte 19 0.026
768
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 18 0.026
769
PRQ001 Paraquat Lung 17 0.026
Content
Loading form....