Search results for Simvastatin

833 hits were found for Simvastatin

# Family MCID Name MIFTS Score
1
OBS302 Obsolete: Simvastatin Toxicity 1 2.762
2
c OBS358 Obsolete: Susceptibility to Adverse Reaction Due to Simvastatin Treatment 1 2.762
3
c HYP836 Hypercholesterolemia, Familial, 1 74 0.741
4
LPD008 Lipid Metabolism Disorder 64 0.443
5
c HYP272 Hypercholesterolemia, Familial, 3 44 0.415
6
P CRN300 Coronary Heart Disease 1 59 0.391
7
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.348
8
P CRN018 Coronary Artery Anomaly 67 0.340
9
P MYP004 Myopathy 63 0.330
10
HYP081 Hypolipoproteinemia 51 0.326
11
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.321
12
ATH013 Atherosclerosis Susceptibility 68 0.314
13
ISC004 Ischemia 62 0.298
14
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.287
15
ART140 Arteries, Anomalies of 60 0.281
16
P HRT032 Heart Disease 78 0.278
17
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.276
18
P DBT009 Diabetes Mellitus 66 0.251
19
c FML035 Familial Hyperlipidemia 56 0.246
20
c FML021 Familial Hypercholesterolemia 67 0.243
21
CRB039 Cerebrovascular Disease 71 0.236
22
P VSC007 Vascular Disease 65 0.232
23
P MYC007 Myocardial Infarction 74 0.227
24
c HYP595 Hypertension, Essential 87 0.224
25
STR067 Stroke, Ischemic 82 0.223
26
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.220
27
P KDN018 Kidney Disease 73 0.218
28
P HYP750 Hypertriglyceridemia, Familial 62 0.217
29
P PRD008 Periodontitis 66 0.180
30
ANG054 Angina Pectoris 66 0.174
31
ADL002 Adult Syndrome 62 0.171
32
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.171
33
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.171
34
c CHR684 Chronic Kidney Disease 68 0.163
35
PRP027 Peripheral Vascular Disease 72 0.157
36
OBS529 Obsolete: Combined Hyperlipidemia 22 0.155
37
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.153
38
LVR012 Liver Cirrhosis 67 0.151
39
48X005 48,xyyy 37 0.151
40
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.149
41
P PLM037 Pulmonary Hypertension 69 0.147
42
CNG034 Congestive Heart Failure 69 0.147
43
c ACT210 Acute Respiratory Distress Syndrome 59 0.147
44
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.147
45
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.147
46
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.147
47
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.147
48
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.147
49
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.147
50
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.147
51
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.147
52
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.147
53
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.147
54
P CLR023 Colorectal Cancer 100 0.145
55
P LVR013 Liver Disease 71 0.145
56
P MYS005 Myositis 54 0.145
57
c ACT071 Acute Kidney Failure 60 0.141
58
c HYP740 Hyperlipoproteinemia, Type V 53 0.141
59
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.136
60
BRN071 Brain Injury 51 0.136
61
BNR002 Bone Resorption Disease 51 0.136
62
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.136
63
P MLT020 Multiple Sclerosis 73 0.134
64
DWN001 Down Syndrome 70 0.134
65
P PLY011 Polycystic Ovary Syndrome 58 0.134
66
TRM010 Traumatic Brain Injury 54 0.134
67
PRP080 Peripheral Artery Disease 51 0.134
68
P ALZ034 Alzheimer Disease 90 0.132
69
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.132
70
CYT002 Cytokine Deficiency 46 0.132
71
PRT013 Portal Hypertension 61 0.129
72
P TRN020 Turner Syndrome 66 0.127
73
INT007 Intermediate Coronary Syndrome 58 0.124
74
END030 End Stage Renal Failure 60 0.122
75
c PRD040 Periodontitis, Chronic 56 0.122
76
P BRS047 Breast Cancer 99 0.119
77
MYL069 Myeloma, Multiple 85 0.119
78
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.119
79
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.119
80
P HYP086 Hypothyroidism 70 0.117
81
HYP066 Hyperglycemia 63 0.117
82
P PRS040 Prostate Cancer 97 0.114
83
LNG099 Lung Disease 62 0.114
84
P LNG032 Lung Cancer 99 0.111
85
FTT001 Fatty Liver Disease 63 0.111
86
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.111
87
c ACT075 Acute Myocardial Infarction 59 0.111
88
c MCR113 Microvascular Complications of Diabetes 3 55 0.111
89
c MCR120 Microvascular Complications of Diabetes 7 48 0.111
90
c MCR130 Microvascular Complications of Diabetes 6 42 0.111
91
c MCR133 Microvascular Complications of Diabetes 4 42 0.111
92
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.109
93
ATM095 Autoimmune Disease 62 0.109
94
c ACT027 Acute Pancreatitis 60 0.109
95
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.109
96
P OST002 Osteoporosis 79 0.106
97
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.106
98
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.106
99
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.103
100
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.103
101
CHL079 Children's Interstitial Lung Disease 27 0.103
102
P MCR115 Microvascular Complications of Diabetes 5 67 0.100
103
P LPS004 Lupus Erythematosus 62 0.100
104
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.100
105
P RHM011 Rheumatoid Arthritis 82 0.096
106
c SML038 Small Cell Cancer of the Lung 67 0.096
107
INC002 Inclusion Body Myositis 66 0.096
108
P NPH012 Nephrotic Syndrome 65 0.096
109
c RHB024 Rhabdomyosarcoma 2 64 0.096
110
P BCL017 B-Cell Lymphoma 61 0.096
111
P PNC044 Pancreatitis 61 0.096
112
ANR040 Aneurysm 60 0.096
113
GLC003 Glucose Intolerance 55 0.096
114
DPR016 Depression 64 0.093
115
SPN186 Spinal Cord Injury 63 0.093
116
MNT002 Mental Depression 60 0.093
117
P ALP008 Alopecia 58 0.093
118
c LRG017 Large Intestine Cancer 53 0.093
119
P IDP024 Idiopathic Inflammatory Myopathy 49 0.093
120
HYP043 Hyperandrogenism 48 0.093
121
P OVR096 Overlap Myositis 28 0.093
122
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.093
123
c SYS001 Systemic Lupus Erythematosus 88 0.090
124
ART016 Aortic Aneurysm 71 0.090
125
SMT004 Smith-Lemli-Opitz Syndrome 67 0.090
126
P ALP009 Alopecia Areata 61 0.090
127
BRN004 Brain Edema 57 0.090
128
P ART021 Arteriosclerosis 56 0.090
129
P SCK005 Sickle Cell Disease 53 0.090
130
c HNT004 Huntington Disease-Like 2 48 0.090
131
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.090
132
c HNT011 Huntington Disease-Like 3 37 0.090
133
P ART022 Arthritis 71 0.086
134
P END044 Endometriosis 63 0.086
135
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.086
136
CRT016 Carotid Artery Disease 53 0.086
137
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.086
138
CRB004 Cerebral Artery Occlusion 38 0.086
139
c PLY105 Polycystic Ovary Syndrome 1 38 0.086
140
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.086
141
P PNC035 Pancreatic Cancer 86 0.083
142
P PRK057 Parkinson Disease, Late-Onset 77 0.083
143
P SCH015 Schizophrenia 76 0.083
144
LPT014 Leptin Deficiency or Dysfunction 72 0.083
145
P HPT021 Hepatitis 69 0.083
146
OST159 Osteogenic Sarcoma 67 0.083
147
P GLM045 Glioma 64 0.083
148
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.083
149
P CRD132 Cardiac Conduction Defect 61 0.083
150
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.083
151
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.083
152
P NRP001 Neuropathy 57 0.083
153
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.083
154
HMC014 Homocysteinemia 54 0.083
155
IMP005 Impotence 53 0.083
156
LMB062 Limb Ischemia 50 0.083
157
GLL048 Glial Tumor 48 0.083
158
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.083
159
TXC005 Toxic Shock Syndrome 63 0.079
160
TRN015 Transient Cerebral Ischemia 62 0.079
161
P DRM010 Dermatomyositis 62 0.079
162
VRC005 Varicose Veins 61 0.079
163
HYP266 Hypoxia 58 0.079
164
HYP005 Hypokalemia 55 0.079
165
P OPT009 Optic Neuritis 55 0.079
166
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.079
167
c GLL024 Gallbladder Disease 1 53 0.079
168
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.079
169
NRT004 Neuritis 52 0.079
170
c SYS043 Systemic Lupus Erythematosus 1 39 0.079
171
CYT018 Cytochrome P450 2d6 Variant 28 0.079
172
AST005 Asthma 80 0.075
173
DFC004 Deficiency Anemia 77 0.075
174
P PNM007 Pneumonia 71 0.075
175
P ATR011 Atrial Fibrillation 67 0.075
176
c MCR129 Microvascular Complications of Diabetes 1 67 0.075
177
P PLM036 Pulmonary Fibrosis 66 0.075
178
P ADN016 Adenocarcinoma 65 0.075
179
IDP011 Idiopathic Interstitial Pneumonia 65 0.075
180
P ENC018 Encephalopathy 64 0.075
181
P CTR002 Cataract 62 0.075
182
THR024 Thrombosis 58 0.075
183
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.075
184
LNG031 Lung Benign Neoplasm 52 0.075
185
P CHR345 Chronic Pain 52 0.075
186
CRT013 Carotid Stenosis 50 0.075
187
PRD004 Prediabetes Syndrome 49 0.075
188
P INT260 Intracranial Berry Aneurysm 38 0.075
189
c LKM071 Leukemia, Chronic Lymphocytic 81 0.070
190
c ATR087 Atrial Standstill 1 76 0.070
191
c THR092 Thrombophilia Due to Thrombin Defect 74 0.070
192
P CNR004 Cone-Rod Dystrophy 2 72 0.070
193
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.070
194
PSY004 Psychotic Disorder 68 0.070
195
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.070
196
c ART101 Aortic Valve Disease 2 67 0.070
197
P NRB010 Neuroblastoma 1 66 0.070
198
ALL026 Allergic Hypersensitivity Disease 65 0.070
199
INT002 Intermittent Claudication 60 0.070
200
P ALC033 Alcohol Use Disorder 58 0.070
201
ALL006 Allergic Asthma 56 0.070
202
P LYM031 Lymphocytic Leukemia 56 0.070
203
P RCT021 Rectum Cancer 54 0.070
204
LMY002 Leiomyoma 52 0.070
205
SCH003 Schizophreniform Disorder 49 0.070
206
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.070
207
c LKM004 Leukemia, B-Cell, Chronic 35 0.070
208
P HPT023 Hepatocellular Carcinoma 99 0.066
209
P GST053 Gastric Cancer 85 0.066
210
P RSP003 Respiratory Failure 75 0.066
211
GLB002 Glioblastoma 74 0.066
212
SVR004 Severe Combined Immunodeficiency 74 0.066
213
SCK003 Sickle Cell Anemia 74 0.066
214
P RTN024 Retinoblastoma 74 0.066
215
P MJR001 Major Depressive Disorder 69 0.066
216
ALC007 Alcohol Dependence 68 0.066
217
HYP056 Hypoglycemia 68 0.066
218
P CLC063 Celiac Disease 1 66 0.066
219
GLB015 Glioblastoma Multiforme 60 0.066
220
HMR039 Hemorrhage, Intracerebral 59 0.066
221
P SZR006 Seizure Disorder 59 0.066
222
P GLM007 Glomerulonephritis 58 0.066
223
P UVT001 Uveitis 58 0.066
224
P INF037 Inflammatory Bowel Disease 57 0.066
225
P PLY019 Polyneuropathy 55 0.066
226
LPD009 Lipid Storage Disease 49 0.066
227
ART004 Aortic Atherosclerosis 47 0.066
228
c FML008 Familial Retinoblastoma 46 0.066
229
c PCH010 Pachyonychia Congenita 3 43 0.066
230
ALL014 Allergic Encephalomyelitis 40 0.066
231
c HMG029 Hemoglobin Se Disease 40 0.066
232
SPR126 Superior Semicircular Canal Dehiscence 39 0.066
233
c PRS136 Prostate Cancer, Hereditary, 6 34 0.066
234
c PRS130 Prostate Cancer, Hereditary, 8 33 0.066
235
CYS001 Cystic Fibrosis 84 0.061
236
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.061
237
P CRD119 Cardiac Arrest 71 0.061
238
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.061
239
DSS008 Disease of Mental Health 66 0.061
240
P OCL013 Oculodentodigital Dysplasia 65 0.061
241
P NTR004 Neutropenia 64 0.061
242
DRM006 Dermatitis 63 0.061
243
CLT003 Colitis 63 0.061
244
P RHB003 Rhabdomyosarcoma 62 0.061
245
OST003 Osteonecrosis 62 0.061
246
c SCL052 Scleroderma, Familial Progressive 62 0.061
247
ACQ007 Acquired Immunodeficiency Syndrome 61 0.061
248
BND020 Bone Disease 60 0.061
249
P EXN002 Exanthem 58 0.061
250
PRM236 Primary Biliary Cholangitis 57 0.061
251
BCT022 Bacterial Infectious Disease 57 0.061
252
LMY014 Leiomyoma, Uterine 57 0.061
253
PRP030 Purpura 56 0.061
254
CMR002 Coumarin Resistance 56 0.061
255
DBT010 Diabetic Neuropathy 56 0.061
256
P DRR001 Diarrhea 55 0.061
257
P PRM006 Primary Biliary Cirrhosis 54 0.061
258
P HYP040 Hypospadias 54 0.061
259
CRN030 Coronary Stenosis 49 0.061
260
ESP002 Esophageal Varix 49 0.061
261
DBT004 Diabetic Polyneuropathy 48 0.061
262
c PRM038 Primary Agammaglobulinemia 45 0.061
263
P GLM044 Glomerular Disease 42 0.061
264
c MCR112 Microvascular Complications of Diabetes 2 42 0.061
265
FML235 Familial Combined Hyperlipoproteinemia 29 0.061
266
c TBR025 Tuberous Sclerosis 1 74 0.056
267
HMN044 Human Immunodeficiency Virus Type 1 73 0.056
268
P TBR001 Tuberous Sclerosis 72 0.056
269
MSC157 Muscular Dystrophy, Duchenne Type 70 0.056
270
RCK004 Rickets 70 0.056
271
c TBR026 Tuberous Sclerosis 2 69 0.056
272
P LKM002 Leukemia 69 0.056
273
P DMN002 Dementia 68 0.056
274
P HYD006 Hydrocephalus 68 0.056
275
P GLM040 Glioma Susceptibility 1 68 0.056
276
MLN008 Melanoma 68 0.056
277
P MSC005 Muscular Dystrophy 68 0.056
278
LYM007 Lymphangioleiomyomatosis 67 0.056
279
CLF027 Cleft Palate, Isolated 67 0.056
280
MSC007 Muscle Hypertrophy 65 0.056
281
P PSR002 Psoriasis 63 0.056
282
GT001 Gout 63 0.056
283
BRS099 Breast Ductal Carcinoma 63 0.056
284
CHL068 Cholestasis 61 0.056
285
c HPT003 Hepatitis a 60 0.056
286
HPT019 Hepatic Encephalopathy 60 0.056
287
P OPT006 Optic Nerve Disease 59 0.056
288
P BPL003 Bipolar Disorder 59 0.056
289
VSL002 Visual Epilepsy 58 0.056
290
IRN002 Iron Metabolism Disease 58 0.056
291
DCT002 Ductal Carcinoma in Situ 57 0.056
292
VSC002 Vascular Dementia 57 0.056
293
RHM027 Rheumatic Disease 56 0.056
294
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.056
295
HRT012 Heart Valve Disease 56 0.056
296
c CNG216 Congenital Hydrocephalus 55 0.056
297
P PLM034 Pulmonary Emphysema 55 0.056
298
P INS002 in Situ Carcinoma 55 0.056
299
DMY004 Demyelinating Disease 54 0.056
300
OCL069 Ocular Motor Apraxia 53 0.056
301
NNL006 Non-Alcoholic Steatohepatitis 53 0.056
302
P VNB005 Van Buchem Disease 52 0.056
303
DYS014 Dyspepsia 51 0.056
304
c BRS049 Breast Carcinoma in Situ 51 0.056
305
PST011 Pustulosis of Palm and Sole 51 0.056
306
URM002 Uremia 50 0.056
307
HYP748 Hypertelorism 50 0.056
308
P OPT048 Opitz-Gbbb Syndrome 50 0.056
309
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.056
310
ENT004 Enthesopathy 46 0.056
311
HPT004 Hepatic Coma 42 0.056
312
c MJR024 Major Affective Disorder 9 42 0.056
313
c BRT038 Baraitser-Winter Syndrome 1 41 0.056
314
MYF001 Myofibroma 40 0.056
315
c MJR022 Major Affective Disorder 8 39 0.056
316
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.056
317
P OVR042 Ovarian Cancer 89 0.050
318
c DLT002 Dilated Cardiomyopathy 81 0.050
319
OST012 Osteoarthritis 80 0.050
320
INS024 Insulin-Like Growth Factor I 79 0.050
321
P BLD134 Bladder Cancer 79 0.050
322
P LNG064 Lung Cancer Susceptibility 3 79 0.050
323
P MDL005 Medulloblastoma 78 0.050
324
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.050
325
P NRF023 Neurofibromatosis, Type Ii 77 0.050
326
c MGR028 Migraine with or Without Aura 1 70 0.050
327
c PNC108 Pancreatitis, Hereditary 70 0.050
328
PRT036 Peritonitis 66 0.050
329
PRT037 Pertussis 66 0.050
330
P PRS038 Personality Disorder 66 0.050
331
CHG001 Chagas Disease 66 0.050
332
P CRB048 Cerebral Cavernous Malformations 65 0.050
333
FCT007 Factor Vii Deficiency 65 0.050
334
P PRP019 Peripheral Nervous System Disease 64 0.050
335
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.050
336
c HPT016 Hepatitis B 63 0.050
337
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.050
338
LYM012 Lymphoplasmacytic Lymphoma 62 0.050
339
NRM005 Neuromuscular Disease 62 0.050
340
c HPT001 Hepatitis C 62 0.050
341
c PNS012 Paine Syndrome 61 0.050
342
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.050
343
P PLY014 Polycystic Kidney Disease 61 0.050
344
CHL123 Chlamydia 60 0.050
345
PLM033 Pulmonary Embolism 60 0.050
346
P INF032 Infertility 60 0.050
347
EYD002 Eye Disease 59 0.050
348
P HDC001 Headache 59 0.050
349
CNS004 Constipation 59 0.050
350
P PRP029 Porphyria 58 0.050
351
ALP097 Alopecia Universalis Congenita 58 0.050
352
CNT047 Contact Dermatitis 58 0.050
353
AGN016 Aging 58 0.050
354
HPT022 Hepatoblastoma 58 0.050
355
ENH001 Enhanced S-Cone Syndrome 56 0.050
356
MCS002 Mucositis 56 0.050
357
PLM010 Pulmonary Edema 56 0.050
358
END040 Endogenous Depression 55 0.050
359
CHR081 Choroideremia 54 0.050
360
c HRM017 Hermansky-Pudlak Syndrome 2 54 0.050
361
MSC190 Muscular Disease 54 0.050
362
P RTN018 Retinal Disease 53 0.050
363
NRT001 Neurotic Disorder 53 0.050
364
GST023 Gastric Ulcer 53 0.050
365
c PST005 Posterior Uveitis 52 0.050
366
RTN003 Retinal Ischemia 52 0.050
367
P LCT001 Lactic Acidosis 52 0.050
368
KRT009 Keratosis 52 0.050
369
RDC002 Radiculopathy 51 0.050
370
LRN003 Learning Disability 51 0.050
371
SCH012 Schizoaffective Disorder 50 0.050
372
c HYP768 Hyperlipoproteinemia, Type I 50 0.050
373
NTR046 Neutrophil Migration 49 0.050
374
RNL077 Renal Fibrosis 49 0.050
375
P HYP121 Hypoalphalipoproteinemia 49 0.050
376
47X002 47,xyy 49 0.050
377
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 47 0.050
378
GRM005 Germ Cell Cancer 47 0.050
379
P CMP008 Compartment Syndrome 45 0.050
380
TND005 Tendinitis 45 0.050
381
DBT002 Diabetic Autonomic Neuropathy 45 0.050
382
P MJR007 Major Affective Disorder 1 44 0.050
383
P MYG005 Myoglobinuria 43 0.050
384
ASP030 Aspirin Resistance 42 0.050
385
GST020 Gastric Antral Vascular Ectasia 42 0.050
386
CRB086 Cerebral Aneurysms 41 0.050
387
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.050
388
49X002 49,xxxxy Syndrome 39 0.050
389
CHL147 Chlamydia Pneumonia 39 0.050
390
c CHR682 Chronic Bilirubin Encephalopathy 36 0.050
391
c MJR008 Major Affective Disorder 2 35 0.050
392
c MJR003 Major Affective Disorder 6 34 0.050
393
c MJR006 Major Affective Disorder 5 34 0.050
394
c MJR023 Major Affective Disorder 7 34 0.050
395
RRS014 Rare Surgical Neurologic Disease 33 0.050
396
INT053 Intracranial Vasospasm 32 0.050
397
ALP048 Alopecia Totalis 31 0.050
398
c MJR004 Major Affective Disorder 4 29 0.050
399
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.050
400
CLS052 Classic Hairy Cell Leukemia 28 0.050
401
c LKM061 Leukemia, Acute Myeloid 84 0.043
402
IMM167 Immune Deficiency Disease 79 0.043
403
P NNN008 Noonan Syndrome 1 76 0.043
404
BRN028 Brain Cancer 75 0.043
405
c HPT073 Hepatitis C Virus 74 0.043
406
c LKM063 Leukemia, Chronic Myeloid 74 0.043
407
P EPL164 Epilepsy 73 0.043
408
ADR007 Adrenoleukodystrophy 72 0.043
409
P HNT016 Huntington Disease 72 0.043
410
BRN024 Bronchitis 70 0.043
411
LYM133 Lymphoma, Hodgkin, Classic 70 0.043
412
c WLM013 Wilms Tumor 1 69 0.043
413
EWN003 Ewing Sarcoma 69 0.043
414
CHL065 Cholangiocarcinoma 68 0.043
415
c FML001 Familial Atrial Fibrillation 67 0.043
416
P HYP098 Hypereosinophilic Syndrome 67 0.043
417
SRC014 Sarcoma 67 0.043
418
P THR014 Thrombocytopenia 67 0.043
419
P PRP003 Porphyria Cutanea Tarda 66 0.043
420
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.043
421
ACH004 Achondroplasia 66 0.043
422
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.043
423
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.043
424
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.043
425
P VSC011 Vasculitis 64 0.043
426
KHL003 Kohlschutter-Tonz Syndrome 63 0.043
427
c PRC016 Pre-Eclampsia 63 0.043
428
c WLM018 Wilms Tumor 5 63 0.043
429
P MVM001 Movement Disease 63 0.043
430
VRL011 Viral Infectious Disease 62 0.043
431
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.043
432
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 62 0.043
433
RHB001 Rhabdoid Cancer 62 0.043
434
CRB011 Cerebrotendinous Xanthomatosis 61 0.043
435
P MYL006 Myeloid Leukemia 61 0.043
436
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.043
437
SQM006 Squamous Cell Carcinoma 60 0.043
438
FBR047 Fibromyalgia 60 0.043
439
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 60 0.043
440
ADN018 Adenoma 60 0.043
441
BRS051 Breast Disease 59 0.043
442
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.043
443
P HYP726 Hypercalcemia, Infantile, 1 58 0.043
444
P SLP005 Sleep Disorder 58 0.043
445
CMM005 Common Cold 57 0.043
446
GST050 Gastrointestinal System Disease 57 0.043
447
P PLY041 Polymyositis 57 0.043
448
P FBR017 Fibrosarcoma 57 0.043
449
c PCH015 Pachyonychia Congenita 1 57 0.043
450
P GRV001 Graves' Disease 57 0.043
451
P CHN012 Chondrosarcoma 57 0.043
452
INT030 Intracranial Aneurysm 57 0.043
453
SFT003 Soft Tissue Sarcoma 57 0.043
454
SPN035 Spindle Cell Sarcoma 57 0.043
455
ACT200 Acute Monoblastic Leukemia 56 0.043
456
CRN239 Carnitine Deficiency, Systemic Primary 56 0.043
457
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.043
458
HYP060 Hyperinsulinism 55 0.043
459
P HYP076 Hyperthyroidism 55 0.043
460
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.043
461
c LKM070 Leukemia, Acute Monocytic 55 0.043
462
PRS045 Prostatic Hypertrophy 55 0.043
463
RHM028 Rheumatic Heart Disease 54 0.043
464
INT079 Intrahepatic Cholangiocarcinoma 54 0.043
465
TXC002 Toxic Encephalopathy 54 0.043
466
CRT017 Cartilage Disease 54 0.043
467
EXP004 Exophthalmos 53 0.043
468
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.043
469
THY030 Thyroid Gland Disease 53 0.043
470
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.043
471
P MNC007 Monocytic Leukemia 52 0.043
472
PRS021 Prostatic Adenoma 52 0.043
473
GSG001 Gas Gangrene 52 0.043
474
GLS018 Glass Syndrome 51 0.043
475
INT253 Intestinal Benign Neoplasm 50 0.043
476
MCR004 Macroglobulinemia 50 0.043
477
c INF145 Infantile Liver Failure Syndrome 1 50 0.043
478
c MLG074 Malignant Mesenchymoma 50 0.043
479
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.043
480
GST049 Gastrointestinal System Cancer 49 0.043
481
c PRM108 Primary Progressive Multiple Sclerosis 49 0.043
482
RTN020 Retinal Vascular Disease 49 0.043
483
DGN001 Degenerative Disc Disease 49 0.043
484
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.043
485
HPT014 Hepatorenal Syndrome 49 0.043
486
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.043
487
c BPL002 Bipolar I Disorder 48 0.043
488
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 48 0.043
489
XNT003 Xanthomatosis 48 0.043
490
BHR001 Behr Syndrome 47 0.043
491
HDN002 Head Injury 47 0.043
492
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.043
493
c RCR022 Recurrent Acute Pancreatitis 46 0.043
494
NPH010 Nephrosclerosis 46 0.043
495
KRT013 Keratolytic Winter Erythema 45 0.043
496
c CLR017 Clear Cell Sarcoma 45 0.043
497
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.043
498
TND004 Tendinopathy 44 0.043
499
SBC016 Subacute Delirium 43 0.043
500
GST071 Gastrointestinal Carcinoma 42 0.043
501
HYP540 Hypertension, Diastolic 41 0.043
502
CRN020 Coronary Restenosis 40 0.043
503
GNR003 Generalized Atherosclerosis 39 0.043
504
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.043
505
ADR022 Adrenomyeloneuropathy 39 0.043
506
RCT020 Rectum Adenocarcinoma 39 0.043
507
ATM052 Autoimmune Disease 1 38 0.043
508
c WLM011 Wilms Tumor 6 38 0.043
509
SCR011 Scrapie 37 0.043
510
HRW001 Hair Whorl 36 0.043
512
c RNG020 Ring Chromosome 4 34 0.043
513
CHN019 Chand Syndrome 31 0.043
514
DMN026 Dementia Pugilistica 28 0.043
515
c PSD047 Pseudo-Turner Syndrome 22 0.043
517
ESP021 Esophageal Cancer 90 0.035
518
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.035
520
ULC004 Ulcerative Colitis 75 0.035
521
ANX010 Anxiety 75 0.035
522
END057 Endometrial Cancer 74 0.035
523
ADN011 Adenoid Cystic Carcinoma 71 0.035
524
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.035
525
P LYM118 Lymphoma 70 0.035
526
ALL003 Allergic Rhinitis 69 0.035
527
P ATS364 Autism 68 0.035
528
BRK010 Burkitt Lymphoma 68 0.035
529
P NSP012 Nasopharyngeal Carcinoma 67 0.035
530
P SKN015 Skin Carcinoma 67 0.035
531
c DPH024 Diaphragmatic Hernia, Congenital 66 0.035
532
P BLD062 Bile Duct Cancer 66 0.035
533
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.035
534
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.035
535
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.035
536
P THY023 Thymoma 64 0.035
537
LYS012 Lysosomal Acid Lipase Deficiency 63 0.035
538
P HMN010 Hemangioma 62 0.035
539
STT001 Status Epilepticus 61 0.035
540
P ART023 Arthropathy 61 0.035
541
P TXP001 Toxoplasmosis 61 0.035
542
P ADL010 Adult Respiratory Distress Syndrome 61 0.035
543
P KDN017 Kidney Cancer 60 0.035
544
BRN002 Bronchiolitis 60 0.035
545
P RHN004 Rhinitis 59 0.035
546
P CYS018 Cystitis 59 0.035
547
c MST023 Mesothelioma, Malignant 59 0.035
548
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.035
549
NWB001 Newborn Respiratory Distress Syndrome 58 0.035
550
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.035
551
P GST044 Gastritis 58 0.035
552
P PRN023 Prion Disease 57 0.035
553
HMG005 Hemoglobinopathy 57 0.035
554
c BCT007 Bacterial Meningitis 56 0.035
555
P PLY018 Polycythemia 56 0.035
556
P LTR001 Lateral Sclerosis 56 0.035
557
GRN034 Grange Syndrome 55 0.035
558
BRN012 Bronchiolitis Obliterans 55 0.035
559
c THY107 Thymoma, Familial 55 0.035
560
ACT058 Active Peptic Ulcer Disease 55 0.035
561
P OVR049 Ovarian Disease 55 0.035
562
PRP016 Paraplegia 54 0.035
563
P ANG015 Angioedema 54 0.035
564
P DBT005 Diabetes Insipidus 54 0.035
565
c ACT134 Acute Liver Failure 53 0.035
566
LYS002 Lysosomal Storage Disease 52 0.035
567
P HMC002 Homocystinuria 52 0.035
568
MYM001 Myoma 52 0.035
569
P CPL006 Capillary Hemangioma 52 0.035
570
GST037 Gastroparesis 52 0.035
571
P THR015 Thrombophilia 51 0.035
572
STM007 Stomatitis 51 0.035
573
ILS001 Ileus 51 0.035
574
HYP088 Hyper-Igd Syndrome 51 0.035
575
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.035
576
P PRC012 Pericardial Effusion 51 0.035
577
ACR041 Acromelic Frontonasal Dysostosis 50 0.035
578
PRS129 Prostatic Hyperplasia, Benign 49 0.035
579
P RNV001 Renovascular Hypertension 49 0.035
580
CVR006 Cavernous Hemangioma 49 0.035
581
P OBS001 Obstructive Jaundice 49 0.035
582
HYP781 Hypoascorbemia 48 0.035
583
ESN015 Eosinophilic Fasciitis 48 0.035
584
WTH001 Withdrawal Disorder 47 0.035
585
P BNG032 Benign Mesothelioma 47 0.035
586
FSC004 Fasciitis 47 0.035
587
GLC008 Glucose Metabolism Disease 47 0.035
588
URT010 Ureteral Obstruction 46 0.035
589
c MLG068 Malignant Glioma 46 0.035
590
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.035
591
CHL056 Cheilitis 46 0.035
592
ATX019 Ataxia with Vitamin E Deficiency 46 0.035
593
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.035
594
RTR008 Root Resorption 44 0.035
595
HMP001 Hemopericardium 44 0.035
596
ATN004 Autonomic Neuropathy 43 0.035
597
P CRB154 Cerebrocostomandibular Syndrome 43 0.035
598
SYS003 Systolic Heart Failure 43 0.035
599
P PRL003 Proliferative Glomerulonephritis 43 0.035
600
TRP009 Triple X Syndrome 42 0.035
601
ANG049 Angioedema Induced by Ace Inhibitors 41 0.035
602
KLD004 Keloid Disorder 41 0.035
603
c OVR114 Ovarian Cancer 1 39 0.035
604
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 36 0.035
605
INF013 Inferior Myocardial Infarction 35 0.035
606
CND006 Candida Glabrata 33 0.035
607
CHR463 Chronic Actinic Dermatitis 32 0.035
608
RSP007 Respiratory Distress Syndrome, Infant 31 0.035
609
c CLB022 Coloboma, Ocular, Autosomal Recessive 27 0.035
610
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.035
611
P CRT085 Carotid Intimal Medial Thickness 2 25 0.035
612
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 18 0.035
613
CNT023 Central Nervous System Hemangioma 13 0.035
614
P ATX030 Ataxia-Telangiectasia 83 0.025
615
MLR004 Malaria 82 0.025
616
CRV035 Cervical Cancer 77 0.025
617
P APL001 Aplastic Anemia 76 0.025
618
CRH001 Crohn's Disease 75 0.025
619
c HMC039 Hemochromatosis, Type 1 73 0.025
620
P FML011 Familial Adenomatous Polyposis 73 0.025
621
c BTT014 Beta-Thalassemia 73 0.025
622
PLM001 Pulmonary Tuberculosis 72 0.025
623
P GRF003 Graft-Versus-Host Disease 71 0.025
624
P AMY004 Amyloidosis 71 0.025
625
P PHC003 Pheochromocytoma 71 0.025
626
PLY001 Polycythemia Vera 70 0.025
627
P FML018 Familial Mediterranean Fever 70 0.025
628
P INF038 Influenza 69 0.025
629
P MTC003 Metachromatic Leukodystrophy 69 0.025
630
PNC129 Pancreatic Adenocarcinoma 69 0.025
631
P FRG001 Fragile X Syndrome 69 0.025
632
P MYS003 Myasthenia Gravis 68 0.025
633
P HYP061 Hypertrophic Cardiomyopathy 68 0.025
634
GST092 Gastroesophageal Reflux 68 0.025
635
c JVN010 Juvenile Rheumatoid Arthritis 67 0.025
636
P CNJ013 Conjunctivitis 67 0.025
637
P ASP006 Aspergillosis 67 0.025
638
BRR014 Barrett Esophagus 67 0.025
639
P MNN013 Meningitis 67 0.025
640
SVR097 Severe Cutaneous Adverse Reaction 66 0.025
641
SKN016 Skin Disease 64 0.025
642
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.025
643
LSH001 Leishmaniasis 64 0.025
644
HSH003 Hashimoto Thyroiditis 63 0.025
645
ACT119 Acute Promyelocytic Leukemia 63 0.025
646
c ATM011 Autoimmune Hepatitis 63 0.025
647
MDD011 Mood Disorder 62 0.025
648
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.025
649
c VSC019 Vesicoureteral Reflux 1 62 0.025
650
P THL005 Thalassemia 62 0.025
651
TTN003 Tetanus 62 0.025
652
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.025
653
THY029 Thyroid Carcinoma 62 0.025
654
CRD223 Cardiac Arrhythmia 61 0.025
655
LKD001 Leukodystrophy 61 0.025
656
P URT039 Urticaria 61 0.025
657
CTN007 Cutaneous Leishmaniasis 61 0.025
659
P EPN002 Ependymoma 61 0.025
660
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.025
661
HLC007 Helicobacter Pylori Infection 61 0.025
662
CHR619 Chromosome 2q35 Duplication Syndrome 61 0.025
663
c LPM012 Lipomatosis, Multiple 60 0.025
664
P BRN022 Bronchiectasis 60 0.025
665
P MYC008 Myocarditis 60 0.025
666
GST045 Gastroenteritis 60 0.025
667
P MLG056 Malignant Hyperthermia 60 0.025
668
c HRD002 Hereditary Angioedema 59 0.025
669
P BRS044 Breast Adenocarcinoma 59 0.025
670
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.025
671
SPN027 Spinal Stenosis 58 0.025
672
ADR005 Adrenal Carcinoma 58 0.025
673
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 58 0.025
674
DSS009 Disseminated Intravascular Coagulation 58 0.025
675
MVL001 Mevalonic Aciduria 58 0.025
676
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.025
677
SCH014 Schistosomiasis 57 0.025
678
GLL018 Gallbladder Cancer 57 0.025
679
CMP010 Complex Regional Pain Syndrome 57 0.025
680
HRY003 Hairy Cell Leukemia 57 0.025
681
ERY003 Erythema Multiforme 57 0.025
682
P BNC003 Bone Cancer 56 0.025
683
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.025
684
ATR057 Atrioventricular Block 56 0.025
685
c NPH055 Nephrotic Syndrome, Type 1 56 0.025
686
PHR003 Pharyngitis 56 0.025
687
P PNM006 Pneumoconiosis 55 0.025
688
SYN007 Synovitis 55 0.025
689
AMN003 Amnestic Disorder 55 0.025
690
P LCH002 Lichen Planus 55 0.025
691
LST001 Listeriosis 55 0.025
692
HMP005 Hemiplegia 55 0.025
693
GNR004 Generalized Anxiety Disorder 55 0.025
694
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.025
695
HMT018 Hematopoietic Stem Cell Transplantation 54 0.025
696
P MMB011 Membranous Nephropathy 54 0.025
697
INT075 Intracranial Hypertension 54 0.025
698
GTR002 Goiter 54 0.025
699
AMN001 Amenorrhea 54 0.025
700
P PTS002 Ptosis 53 0.025
701
TLN003 Telangiectasis 53 0.025
702
c CRB191 Cerebral Cavernous Malformations 2 53 0.025
703
CHR100 Chronic Ulcer of Skin 53 0.025
704
FRZ001 Frozen Shoulder 53 0.025
705
P ECL001 Eclampsia 53 0.025
706
P TMP001 Temporal Lobe Epilepsy 53 0.025
707
CLF001 Cleft Lip 53 0.025
708
P MTC133 Mitochondrial Myopathy 53 0.025
709
MCP006 Mucoepidermoid Carcinoma 53 0.025
710
DYS073 Dysphagia 52 0.025
711
c ACT135 Acute Graft Versus Host Disease 52 0.025
712
HYP014 Hyperuricemia 52 0.025
713
P THY032 Thyroiditis 52 0.025
714
THR004 Thrombocytosis 52 0.025
715
P CTN015 Cutaneous T Cell Lymphoma 52 0.025
716
MCL006 Macular Retinal Edema 52 0.025
717
c INF023 Inflammatory Breast Carcinoma 52 0.025
718
P AST007 Astrocytoma 52 0.025
719
P MSC003 Muscular Atrophy 52 0.025
720
AZS001 Azoospermia 51 0.025
722
ANK001 Ankylosis 51 0.025
723
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.025
724
c PYR010 Peyronie's Disease 51 0.025
725
ADR040 Adrenal Gland Pheochromocytoma 51 0.025
726
CHL004 Cholelithiasis 50 0.025
727
P PST095 Post-Thrombotic Syndrome 50 0.025
728
P END047 Endophthalmitis 50 0.025
729
P AGG001 Aggressive Periodontitis 50 0.025
730
ILT001 Ileitis 50 0.025
731
P ESN008 Eosinophilic Pneumonia 50 0.025
732
PLR008 Pleurisy 50 0.025
733
CRD137 Cardiogenic Shock 50 0.025
734
P CTN003 Cutaneous Lupus Erythematosus 50 0.025
735
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.025
736
TST044 Testicular Torsion 49 0.025
737
DDN011 Duodenal Atresia 49 0.025
738
c MTR002 Mitral Valve Insufficiency 49 0.025
739
HMG002 Hemoglobinuria 49 0.025
740
P ATR005 Atrophic Gastritis 49 0.025
741
ATS010 Autosomal Recessive Disease 49 0.025
742
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.025
743
THR013 Thoracic Outlet Syndrome 49 0.025
744
TST015 Testicular Disease 49 0.025
745
c BNG030 Benign Ependymoma 48 0.025
746
P DPY001 Dupuytren Contracture 48 0.025
747
ATN005 Autonomic Dysfunction 48 0.025
748
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.025
749
CRN019 Coronary Artery Vasospasm 48 0.025
750
CNZ001 Coenzyme Q10 Deficiency Disease 48 0.025
751
PLP001 Pulpitis 48 0.025
752
CHR074 Choriocarcinoma 47 0.025
753
INT010 Intracranial Embolism 47 0.025
754
VTM033 Vitamin K Deficiency Bleeding 47 0.025
755
HYP025 Hyperphosphatemia 47 0.025
756
P ART018 Aortic Valve Insufficiency 47 0.025
757
P RNL015 Renal Hypertension 47 0.025
758
HLX001 Helix Syndrome 46 0.025
759
FLL008 Folliculitis 46 0.025
760
ANT018 Anthracosis 46 0.025
761
P RPP006 Rippling Muscle Disease 2 46 0.025
762
PNM013 Pneumococcal Meningitis 45 0.025
763
MYC005 Myocardial Stunning 45 0.025
764
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 45 0.025
765
PRT035 Peritoneum Cancer 45 0.025
766
c NPH049 Nephrotic Syndrome, Type 2 45 0.025
767
BCK006 Back Pain 44 0.025
768
ANX004 Anoxia 44 0.025
769
OBS082 Obstructive Nephropathy 44 0.025
770
BCT021 Bacterial Sepsis 44 0.025
771
P ERY008 Erythromelalgia 44 0.025
772
ANC002 Anca-Associated Vasculitis 43 0.025
773
MCR011 Microinvasive Gastric Cancer 43 0.025
774
P AVS003 Avascular Necrosis 43 0.025
775
FLL031 Follicular Adenoma 43 0.025
776
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 43 0.025
777
P KLZ004 Kala-Azar 1 43 0.025
778
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.025
779
TND006 Tendinosis 42 0.025
780
BRS064 Bursitis 42 0.025
781
P MLT008 Multinodular Goiter 42 0.025
782
c VRL005 Viral Pneumonia 42 0.025
783
PPL001 Papillary Adenoma 42 0.025
784
SKN023 Skin Tag 41 0.025
785
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.025
786
NSP002 Nasopharyngitis 41 0.025
787
PLM005 Pleomorphic Lipoma 41 0.025
788
MRP001 Morphine Dependence 41 0.025
789
PRT019 Protein-Losing Enteropathy 41 0.025
790
P TST026 Testicular Germ Cell Cancer 40 0.025
791
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.025
792
WLL004 Wallerian Degeneration 40 0.025
793
HMR023 Hemorrhagic Cystitis 40 0.025
794
ALV001 Alveolar Periostitis 39 0.025
795
P TRC005 Tracheal Stenosis 39 0.025
796
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.025
797
STR077 Streptococcal Toxic-Shock Syndrome 38 0.025
798
MNN017 Mononeuropathy 38 0.025
799
DNT006 Dental Pulp Necrosis 37 0.025
800
BRR002 Barrett's Adenocarcinoma 36 0.025
801
AMR003 Amaurosis Fugax 36 0.025
802
CHR178 Chromosomal Triplication 36 0.025
803
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 36 0.025
804
XNT009 Xanthoma Disseminatum 36 0.025
805
CVR010 Cavernous Malformation 36 0.025
806
c ATM100 Autoimmune Optic Neuritis 35 0.025
807
ISL077 Isolated Hyperckemia 35 0.025
808
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.025
809
ATN021 Autoinflammatory Syndrome 33 0.025
810
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.025
811
LCH013 Lichen Planus Pemphigoides 33 0.025
812
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.025
813
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.025
814
P HRD022 Hordeolum 32 0.025
815
c PRM339 Primary Glomerular Disease 32 0.025
816
CHL070 Cholesterol Embolism 32 0.025
817
LNG091 Lung Mucoepidermoid Carcinoma 31 0.025
818
PLY150 Polykaryocytosis Inducer 31 0.025
819
ERY066 Erythema Multiforme Major 29 0.025
820
DFC001 Defective Apolipoprotein B-100 27 0.025
821
DFF010 Diffuse Alopecia Areata 27 0.025
822
P MRL001 Meralgia Paresthetica 27 0.025
823
P CLL020 Collagenopathy Type 2 Alpha 1 25 0.025
824
ADG002 Audiogenic Seizures 25 0.025
825
c PRM243 Primary Bone Cancer 25 0.025
826
DRG016 Drug Induced Dyskinesia 24 0.025
827
c RNG021 Ring Chromosome 5 24 0.025
828
HML018 Homologous Wasting Disease 22 0.025
829
CD4008 Cd4/cd8 T-Cell Ratio 21 0.025
830
IDP022 Idiopathic Spinal Cord Herniation 17 0.025
832
ODN022 Odontoid Hypoplasia 16 0.025
833
STT044 Statin Toxicity 12 0.025
Content
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