Search results for Simvastatin

838 hits were found for Simvastatin

# Family MCID Name MIFTS Score
1
c HYP836 Hypercholesterolemia, Familial, 1 73 0.709
2
LPD008 Lipid Metabolism Disorder 62 0.425
3
c HYP272 Hypercholesterolemia, Familial, 3 44 0.400
4
P CRN300 Coronary Heart Disease 1 63 0.364
5
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.332
6
LPP008 Lipoprotein Quantitative Trait Locus 62 0.323
7
P MYP004 Myopathy 70 0.320
8
HYP081 Hypolipoproteinemia 51 0.312
9
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.301
10
ATH013 Atherosclerosis Susceptibility 65 0.294
11
ISC004 Ischemia 58 0.291
12
P CRD246 Cardiovascular System Disease 57 0.275
13
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.264
14
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.261
15
P HRT032 Heart Disease 75 0.257
16
ART140 Arteries, Anomalies of 52 0.255
17
c FML035 Familial Hyperlipidemia 55 0.237
18
P DBT009 Diabetes Mellitus 64 0.235
19
c FML021 Familial Hypercholesterolemia 66 0.233
20
CRB039 Cerebrovascular Disease 67 0.227
21
P MYC007 Myocardial Infarction 70 0.220
22
P VSC007 Vascular Disease 63 0.220
23
STR067 Stroke, Ischemic 81 0.213
24
P KDN018 Kidney Disease 72 0.207
25
c HYP595 Hypertension, Essential 84 0.206
26
P HYP750 Hypertriglyceridemia, Familial 62 0.206
27
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.198
28
P PRD008 Periodontitis 64 0.175
29
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.167
30
ANG054 Angina Pectoris 66 0.165
31
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.162
32
ADL002 Adult Syndrome 70 0.158
33
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.153
34
c CHR684 Chronic Kidney Disease 70 0.151
35
PRP027 Peripheral Vascular Disease 71 0.149
36
LVR012 Liver Cirrhosis 62 0.146
37
CNG034 Congestive Heart Failure 69 0.144
38
P MYS005 Myositis 56 0.142
39
P PLM037 Pulmonary Hypertension 67 0.140
40
P LVR013 Liver Disease 68 0.138
41
48X005 48,xyyy 39 0.136
42
P CLR023 Colorectal Cancer 99 0.134
43
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.134
44
P MLT020 Multiple Sclerosis 72 0.134
45
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.134
46
c ACT071 Acute Kidney Failure 60 0.134
47
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.132
48
c HYP740 Hyperlipoproteinemia, Type V 53 0.132
49
BNR002 Bone Resorption Disease 48 0.129
50
PRT013 Portal Hypertension 59 0.127
51
P PLY011 Polycystic Ovary Syndrome 56 0.127
52
PRP080 Peripheral Artery Disease 53 0.127
53
TRM010 Traumatic Brain Injury 51 0.127
54
P ALZ034 Alzheimer Disease 88 0.125
55
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.125
56
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.125
57
BRN071 Brain Injury 49 0.125
58
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.125
59
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.125
60
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.125
61
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.125
62
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.125
63
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.125
64
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.125
65
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.125
66
CYT002 Cytokine Deficiency 42 0.125
67
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.125
68
P BRS047 Breast Cancer 97 0.120
69
DWN001 Down Syndrome 70 0.120
70
INT007 Intermediate Coronary Syndrome 55 0.118
71
c PRD040 Periodontitis, Chronic 53 0.118
72
P TRN020 Turner Syndrome 67 0.116
73
MYL069 Myeloma, Multiple 85 0.113
74
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.113
75
END086 End Stage Renal Disease 51 0.113
76
P LNG032 Lung Cancer 98 0.111
77
HYP066 Hyperglycemia 61 0.111
78
P PRS040 Prostate Cancer 97 0.108
79
P HYP086 Hypothyroidism 69 0.108
80
LNG099 Lung Disease 60 0.108
81
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.106
82
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.106
83
FTT001 Fatty Liver Disease 61 0.106
84
c ACT075 Acute Myocardial Infarction 57 0.106
85
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.106
86
c MCR113 Microvascular Complications of Diabetes 3 52 0.106
87
c MCR120 Microvascular Complications of Diabetes 7 47 0.106
88
c MCR130 Microvascular Complications of Diabetes 6 41 0.106
89
c MCR133 Microvascular Complications of Diabetes 4 41 0.106
90
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.103
91
ATM095 Autoimmune Disease 62 0.103
92
c ACT027 Acute Pancreatitis 60 0.103
93
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.103
94
P RHM011 Rheumatoid Arthritis 80 0.100
95
P OST002 Osteoporosis 74 0.100
96
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.100
97
c RHB024 Rhabdomyosarcoma 2 67 0.097
98
P MCR115 Microvascular Complications of Diabetes 5 66 0.097
99
P LPS004 Lupus Erythematosus 61 0.097
100
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.097
101
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.097
102
CHL079 Children's Interstitial Lung Disease 26 0.097
103
c SML038 Small Cell Cancer of the Lung 65 0.094
104
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.094
105
P BCL017 B-Cell Lymphoma 58 0.094
106
P ALP008 Alopecia 54 0.094
107
DPR016 Depression 63 0.091
108
P PNC044 Pancreatitis 61 0.091
109
P NPH012 Nephrotic Syndrome 60 0.091
110
ANR040 Aneurysm 59 0.091
111
INC002 Inclusion Body Myositis 58 0.091
112
MNT002 Mental Depression 58 0.091
113
c SYS001 Systemic Lupus Erythematosus 86 0.088
114
SPN186 Spinal Cord Injury 60 0.088
115
P ALP009 Alopecia Areata 60 0.088
116
HYP043 Hyperandrogenism 48 0.088
117
c HYP839 Hyperlipidemia, Familial Combined, 1 29 0.088
118
P OVR096 Overlap Myositis 27 0.088
119
SMT004 Smith-Lemli-Opitz Syndrome 70 0.085
120
P ART022 Arthritis 69 0.085
121
ART016 Aortic Aneurysm 69 0.085
122
VRC005 Varicose Veins 60 0.085
123
BRN004 Brain Edema 56 0.085
124
GLC003 Glucose Intolerance 54 0.085
125
P ART021 Arteriosclerosis 54 0.085
126
c HNT004 Huntington Disease-Like 2 50 0.085
127
P SCK005 Sickle Cell Disease 50 0.085
128
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.085
129
c HNT011 Huntington Disease-Like 3 38 0.085
130
P HPT021 Hepatitis 67 0.082
131
P END044 Endometriosis 63 0.082
132
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.082
133
IMP005 Impotence 52 0.082
134
CRT016 Carotid Artery Disease 52 0.082
135
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.082
136
CRB004 Cerebral Artery Occlusion 45 0.082
137
c PLY105 Polycystic Ovary Syndrome 1 38 0.082
138
P PNC035 Pancreatic Cancer 84 0.078
139
P PRK057 Parkinson Disease, Late-Onset 78 0.078
140
c ATR087 Atrial Standstill 1 75 0.078
141
LPT014 Leptin Deficiency or Dysfunction 74 0.078
142
P SCH015 Schizophrenia 74 0.078
143
P PNM007 Pneumonia 68 0.078
144
OST159 Osteogenic Sarcoma 66 0.078
145
P GLM045 Glioma 63 0.078
146
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.078
147
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.078
148
CRD132 Cardiac Conduction Defect 58 0.078
149
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.078
150
LMB062 Limb Ischemia 55 0.078
151
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.078
152
HMC014 Homocysteinemia 53 0.078
153
PLS009 Plasma Cell Neoplasm 51 0.078
154
GLL048 Glial Tumor 45 0.078
155
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.078
156
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.078
157
P CNR004 Cone-Rod Dystrophy 2 73 0.075
158
P NRB001 Neuroblastoma 72 0.075
159
PSY004 Psychotic Disorder 67 0.075
160
TRN015 Transient Cerebral Ischemia 63 0.075
161
TXC005 Toxic Shock Syndrome 62 0.075
162
P DRM010 Dermatomyositis 61 0.075
163
P OPT009 Optic Neuritis 57 0.075
164
HYP266 Hypoxia 57 0.075
165
P NRP001 Neuropathy 56 0.075
166
BCT022 Bacterial Infectious Disease 56 0.075
167
HYP005 Hypokalemia 55 0.075
168
c GLL024 Gallbladder Disease 1 53 0.075
169
NRT004 Neuritis 52 0.075
170
c SYS043 Systemic Lupus Erythematosus 1 38 0.075
171
CYT018 Cytochrome P450 2d6 Variant 27 0.075
172
AST005 Asthma 76 0.071
173
GLB015 Glioblastoma Multiforme 75 0.071
174
P RSP003 Respiratory Failure 74 0.071
175
DFC004 Deficiency Anemia 70 0.071
176
P MJR001 Major Depressive Disorder 68 0.071
177
c MCR129 Microvascular Complications of Diabetes 1 66 0.071
178
P PLM036 Pulmonary Fibrosis 65 0.071
179
P ADN016 Adenocarcinoma 64 0.071
180
P ENC018 Encephalopathy 61 0.071
181
P CTR002 Cataract 60 0.071
182
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.071
183
P UVT001 Uveitis 57 0.071
184
THR024 Thrombosis 57 0.071
185
ALL006 Allergic Asthma 56 0.071
186
P RCT021 Rectum Cancer 52 0.071
187
LMY002 Leiomyoma 52 0.071
188
ESP002 Esophageal Varix 51 0.071
189
CRT013 Carotid Stenosis 50 0.071
190
PRD004 Prediabetes Syndrome 47 0.071
191
P INT260 Intracranial Berry Aneurysm 39 0.071
192
P GST053 Gastric Cancer 83 0.067
193
P LKM071 Leukemia, Chronic Lymphocytic 79 0.067
194
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.067
195
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.067
196
P ATR011 Atrial Fibrillation 66 0.067
197
c ART101 Aortic Valve Disease 2 65 0.067
198
c DBT099 Diabetes Mellitus, Type I 65 0.067
199
INT002 Intermittent Claudication 61 0.067
200
P MYL006 Myeloid Leukemia 60 0.067
201
P ALC033 Alcohol Use Disorder 58 0.067
202
DSS008 Disease of Mental Health 58 0.067
203
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.067
204
CMR002 Coumarin Resistance 56 0.067
205
SCH003 Schizophreniform Disorder 56 0.067
206
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.067
207
P CHR345 Chronic Pain 44 0.067
208
c PCH010 Pachyonychia Congenita 3 44 0.067
209
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.067
210
P HPT023 Hepatocellular Carcinoma 100 0.062
211
SCK003 Sickle Cell Anemia 74 0.062
212
SVR004 Severe Combined Immunodeficiency 73 0.062
213
c THR092 Thrombophilia Due to Thrombin Defect 73 0.062
214
P RTN024 Retinoblastoma 73 0.062
215
CHL065 Cholangiocarcinoma 68 0.062
216
P CLC063 Celiac Disease 1 66 0.062
217
ALC007 Alcohol Dependence 66 0.062
218
P DMN002 Dementia 66 0.062
219
HYP056 Hypoglycemia 66 0.062
220
P RHB003 Rhabdomyosarcoma 63 0.062
221
OST003 Osteonecrosis 61 0.062
222
P GLM007 Glomerulonephritis 57 0.062
223
HMR039 Hemorrhage, Intracerebral 57 0.062
224
LMY014 Leiomyoma, Uterine 56 0.062
225
P SZR006 Seizure Disorder 56 0.062
226
P PLY019 Polyneuropathy 56 0.062
227
P DRR001 Diarrhea 55 0.062
228
P INF037 Inflammatory Bowel Disease 54 0.062
229
c FML008 Familial Retinoblastoma 53 0.062
230
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.062
231
INT079 Intrahepatic Cholangiocarcinoma 51 0.062
232
LNG031 Lung Benign Neoplasm 51 0.062
233
ART004 Aortic Atherosclerosis 47 0.062
234
SPR126 Superior Semicircular Canal Dehiscence 40 0.062
235
c HMG029 Hemoglobin Se Disease 39 0.062
236
ALL014 Allergic Encephalomyelitis 38 0.062
237
c PRS136 Prostate Cancer, Hereditary, 6 33 0.062
238
c PRS130 Prostate Cancer, Hereditary, 8 32 0.062
239
CYS001 Cystic Fibrosis 81 0.058
240
c TBR025 Tuberous Sclerosis 1 77 0.058
241
P TBR001 Tuberous Sclerosis 70 0.058
242
P MLN008 Melanoma 69 0.058
243
P OCL013 Oculodentodigital Dysplasia 69 0.058
244
LYM007 Lymphangioleiomyomatosis 69 0.058
245
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.058
246
CHG001 Chagas Disease 66 0.058
247
CLT003 Colitis 62 0.058
248
ALL026 Allergic Hypersensitivity Disease 62 0.058
249
P PRM006 Primary Biliary Cirrhosis 62 0.058
250
DRM006 Dermatitis 61 0.058
251
c SCL052 Scleroderma, Familial Progressive 61 0.058
252
ACQ007 Acquired Immunodeficiency Syndrome 60 0.058
253
P BND020 Bone Disease 59 0.058
254
CNS004 Constipation 58 0.058
255
P EXN002 Exanthem 57 0.058
256
P HDC001 Headache 57 0.058
257
END040 Endogenous Depression 55 0.058
258
PRP030 Purpura 54 0.058
259
DBT010 Diabetic Neuropathy 54 0.058
260
NNL006 Non-Alcoholic Steatohepatitis 54 0.058
261
NRT001 Neurotic Disorder 53 0.058
262
CRN030 Coronary Stenosis 50 0.058
263
DBT004 Diabetic Polyneuropathy 49 0.058
264
c DRR009 Diarrhea 6 46 0.058
265
c PRM038 Primary Agammaglobulinemia 44 0.058
266
c MCR112 Microvascular Complications of Diabetes 2 41 0.058
267
c CHR682 Chronic Bilirubin Encephalopathy 39 0.058
268
GLM044 Glomerular Disease 37 0.058
269
P GLM040 Glioma Susceptibility 1 81 0.053
270
IMM167 Immune Deficiency Disease 78 0.053
271
MSC157 Muscular Dystrophy, Duchenne Type 72 0.053
272
c TBR026 Tuberous Sclerosis 2 72 0.053
273
HMN044 Human Immunodeficiency Virus Type 1 71 0.053
274
P EPL164 Epilepsy 71 0.053
275
P LKM002 Leukemia 68 0.053
276
RCK004 Rickets 68 0.053
277
P CRB048 Cerebral Cavernous Malformations 67 0.053
278
P MSC005 Muscular Dystrophy 66 0.053
279
P HYD006 Hydrocephalus 66 0.053
280
PRT037 Pertussis 65 0.053
281
P ADL010 Adult Respiratory Distress Syndrome 65 0.053
282
GT001 Gout 64 0.053
283
MSC007 Muscle Hypertrophy 64 0.053
284
P NTR004 Neutropenia 63 0.053
285
P PSR002 Psoriasis 62 0.053
286
c HPT003 Hepatitis a 62 0.053
287
BRS099 Breast Ductal Carcinoma 62 0.053
288
CHL068 Cholestasis 61 0.053
289
HPT019 Hepatic Encephalopathy 60 0.053
290
P OPT006 Optic Nerve Disease 60 0.053
291
VSL002 Visual Epilepsy 59 0.053
292
DCT002 Ductal Carcinoma in Situ 59 0.053
293
ALP097 Alopecia Universalis Congenita 59 0.053
294
NWB001 Newborn Respiratory Distress Syndrome 58 0.053
295
IRN002 Iron Metabolism Disease 57 0.053
296
VSC002 Vascular Dementia 57 0.053
297
P BPL003 Bipolar Disorder 56 0.053
298
P VNB005 Van Buchem Disease 56 0.053
299
P PLM034 Pulmonary Emphysema 55 0.053
300
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.053
301
P INS002 in Situ Carcinoma 53 0.053
302
HRT012 Heart Valve Disease 53 0.053
303
P RTN018 Retinal Disease 53 0.053
304
DMY004 Demyelinating Disease 52 0.053
305
PST011 Pustulosis of Palm and Sole 52 0.053
306
OCL069 Ocular Motor Apraxia 51 0.053
307
c PRM108 Primary Progressive Multiple Sclerosis 51 0.053
308
c BRS049 Breast Carcinoma in Situ 51 0.053
309
ENT004 Enthesopathy 49 0.053
310
47X002 47,xyy 49 0.053
311
URM002 Uremia 49 0.053
312
LPD009 Lipid Storage Disease 46 0.053
313
P OPT048 Opitz-Gbbb Syndrome 46 0.053
314
HPT004 Hepatic Coma 45 0.053
315
MYF001 Myofibroma 45 0.053
316
CVD001 Covid-19 44 0.053
317
c MJR024 Major Affective Disorder 9 41 0.053
318
c MJR022 Major Affective Disorder 8 38 0.053
319
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.053
320
P OVR042 Ovarian Cancer 88 0.047
321
c LKM061 Leukemia, Acute Myeloid 84 0.047
322
c NRF023 Neurofibromatosis, Type Ii 80 0.047
323
P BLD134 Bladder Cancer 79 0.047
324
c DLT002 Dilated Cardiomyopathy 79 0.047
325
INS024 Insulin-Like Growth Factor I 79 0.047
326
OST012 Osteoarthritis 78 0.047
327
P LNG064 Lung Cancer Susceptibility 3 78 0.047
328
P MDL005 Medulloblastoma 77 0.047
329
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.047
330
c PNC108 Pancreatitis, Hereditary 70 0.047
331
c HYP768 Hyperlipoproteinemia, Type I 67 0.047
332
P CRD119 Cardiac Arrest 67 0.047
333
FCT007 Factor Vii Deficiency 67 0.047
334
c MGR028 Migraine with or Without Aura 1 67 0.047
335
KHL003 Kohlschutter-Tonz Syndrome 65 0.047
336
P PRS038 Personality Disorder 65 0.047
337
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.047
338
PRT036 Peritonitis 64 0.047
339
NRM005 Neuromuscular Disease 64 0.047
340
c HPT001 Hepatitis C 62 0.047
341
P PLY014 Polycystic Kidney Disease 62 0.047
342
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.047
343
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.047
344
P PRP029 Porphyria 62 0.047
345
c PNS012 Paine Syndrome 61 0.047
346
c HPT016 Hepatitis B 59 0.047
347
CHL123 Chlamydia 59 0.047
348
PLM033 Pulmonary Embolism 59 0.047
349
CNT047 Contact Dermatitis 58 0.047
350
EYD002 Eye Disease 58 0.047
351
P PRP019 Peripheral Nervous System Disease 58 0.047
352
CHR081 Choroideremia 57 0.047
353
P INF032 Infertility 57 0.047
354
MCS002 Mucositis 56 0.047
355
HPT022 Hepatoblastoma 56 0.047
356
TND005 Tendinitis 54 0.047
357
PLM010 Pulmonary Edema 54 0.047
358
c PST005 Posterior Uveitis 54 0.047
359
c HRM017 Hermansky-Pudlak Syndrome 2 53 0.047
360
GST023 Gastric Ulcer 53 0.047
361
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.047
362
KRT009 Keratosis 51 0.047
363
P LCT001 Lactic Acidosis 51 0.047
364
P HYP040 Hypospadias 51 0.047
365
SCH012 Schizoaffective Disorder 50 0.047
366
RDC002 Radiculopathy 50 0.047
367
RTN003 Retinal Ischemia 50 0.047
368
NTR046 Neutrophil Migration 50 0.047
369
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.047
370
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 49 0.047
371
P CMP008 Compartment Syndrome 49 0.047
372
LRN003 Learning Disability 49 0.047
373
CHL147 Chlamydia Pneumonia 48 0.047
374
RCT020 Rectum Adenocarcinoma 48 0.047
375
RNL077 Renal Fibrosis 47 0.047
376
LYM012 Lymphoplasmacytic Lymphoma 47 0.047
377
P MYG005 Myoglobinuria 44 0.047
378
P HYP121 Hypoalphalipoproteinemia 43 0.047
379
P MJR007 Major Affective Disorder 1 43 0.047
380
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.047
381
ATX019 Ataxia with Vitamin E Deficiency 42 0.047
382
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.047
383
GST020 Gastric Antral Vascular Ectasia 41 0.047
384
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.047
385
49X006 49, Xxxxy Syndrome 41 0.047
386
DBT002 Diabetic Autonomic Neuropathy 41 0.047
387
CRB086 Cerebral Aneurysms 40 0.047
388
ASP030 Aspirin Resistance 39 0.047
389
c MJR008 Major Affective Disorder 2 35 0.047
390
c MJR023 Major Affective Disorder 7 33 0.047
391
c MJR003 Major Affective Disorder 6 33 0.047
392
c MJR006 Major Affective Disorder 5 33 0.047
393
ALP048 Alopecia Totalis 32 0.047
394
c MJR004 Major Affective Disorder 4 28 0.047
395
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.047
396
CLS052 Classic Hairy Cell Leukemia 27 0.047
397
INT053 Intracranial Vasospasm 24 0.047
398
P NNN008 Noonan Syndrome 1 76 0.041
399
ADR007 Adrenoleukodystrophy 75 0.041
400
BRN028 Brain Cancer 74 0.041
401
c HPT073 Hepatitis C Virus 72 0.041
402
P HNT016 Huntington Disease 72 0.041
403
LYM133 Lymphoma, Hodgkin, Classic 69 0.041
404
EWN003 Ewing Sarcoma 69 0.041
405
BRN024 Bronchitis 68 0.041
406
P THR014 Thrombocytopenia 67 0.041
407
P PRP003 Porphyria Cutanea Tarda 67 0.041
408
P HYP098 Hypereosinophilic Syndrome 67 0.041
409
ACH004 Achondroplasia 66 0.041
410
c FML001 Familial Atrial Fibrillation 65 0.041
411
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.041
412
SRC014 Sarcoma 65 0.041
413
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.041
414
c WLM013 Wilms Tumor 1 65 0.041
415
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.041
416
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.041
417
CRB011 Cerebrotendinous Xanthomatosis 65 0.041
418
CLF027 Cleft Palate, Isolated 64 0.041
419
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.041
420
c PRC016 Pre-Eclampsia 63 0.041
421
P MVM001 Movement Disease 63 0.041
422
RHB001 Rhabdoid Cancer 63 0.041
423
c SVR001 Severe Acute Respiratory Syndrome 62 0.041
424
P VSC011 Vasculitis 62 0.041
425
CRN239 Carnitine Deficiency, Systemic Primary 62 0.041
426
MSS001 Masa Syndrome 62 0.041
427
NTR005 Nutritional Deficiency Disease 62 0.041
428
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.041
429
WLD007 Waldenstroem's Macroglobulinemia 61 0.041
430
c WLM018 Wilms Tumor 5 61 0.041
431
VRL011 Viral Infectious Disease 61 0.041
432
SQM006 Squamous Cell Carcinoma 60 0.041
433
c PCH015 Pachyonychia Congenita 1 59 0.041
434
P SLP005 Sleep Disorder 59 0.041
435
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 0.041
436
ADN018 Adenoma 59 0.041
437
P HYP726 Hypercalcemia, Infantile, 1 58 0.041
438
FBR047 Fibromyalgia 58 0.041
439
BRS051 Breast Disease 58 0.041
440
GLS018 Glass Syndrome 57 0.041
441
c CHL119 Cholangitis, Primary Sclerosing 57 0.041
442
P PLY041 Polymyositis 57 0.041
443
CMM005 Common Cold 57 0.041
444
c LKM070 Leukemia, Acute Monocytic 57 0.041
445
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.041
446
P CHN012 Chondrosarcoma 56 0.041
447
P FBR017 Fibrosarcoma 56 0.041
448
SFT003 Soft Tissue Sarcoma 56 0.041
449
P NRF002 Neurofibromatosis 56 0.041
450
GST050 Gastrointestinal System Disease 56 0.041
451
INT030 Intracranial Aneurysm 56 0.041
452
AGN016 Aging 56 0.041
453
MCL006 Macular Retinal Edema 55 0.041
454
P GRV001 Graves' Disease 55 0.041
455
P HYP076 Hyperthyroidism 55 0.041
456
HYP060 Hyperinsulinism 54 0.041
457
CRT017 Cartilage Disease 54 0.041
458
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.041
459
PRS045 Prostatic Hypertrophy 53 0.041
460
RHM028 Rheumatic Heart Disease 53 0.041
461
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 0.041
462
P MNC007 Monocytic Leukemia 53 0.041
463
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.041
464
GSG001 Gas Gangrene 53 0.041
465
SPN035 Spindle Cell Sarcoma 53 0.041
466
TXC002 Toxic Encephalopathy 53 0.041
467
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.041
468
EXP004 Exophthalmos 52 0.041
469
THY030 Thyroid Gland Disease 52 0.041
470
ACT200 Acute Monoblastic Leukemia 52 0.041
471
PRS021 Prostatic Adenoma 51 0.041
472
BHR001 Behr Syndrome 51 0.041
473
P CHL066 Cholangitis 51 0.041
474
HPT014 Hepatorenal Syndrome 50 0.041
475
c INF145 Infantile Liver Failure Syndrome 1 50 0.041
476
HYP748 Hypertelorism 50 0.041
477
NPH010 Nephrosclerosis 50 0.041
478
PLP001 Pulpitis 49 0.041
479
XNT003 Xanthomatosis 49 0.041
480
MCR004 Macroglobulinemia 49 0.041
481
GST049 Gastrointestinal System Cancer 49 0.041
482
c BPL002 Bipolar I Disorder 49 0.041
483
WTH001 Withdrawal Disorder 48 0.041
484
P SCL009 Sclerosing Cholangitis 48 0.041
485
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.041
486
DGN001 Degenerative Disc Disease 48 0.041
487
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.041
488
c CNG216 Congenital Hydrocephalus 47 0.041
489
GST071 Gastrointestinal Carcinoma 47 0.041
490
RTN020 Retinal Vascular Disease 46 0.041
491
GNR003 Generalized Atherosclerosis 46 0.041
492
KRT013 Keratolytic Winter Erythema 46 0.041
493
HDN002 Head Injury 46 0.041
494
INT253 Intestinal Benign Neoplasm 45 0.041
495
c CLR017 Clear Cell Sarcoma 45 0.041
496
SPS057 Spasticity 45 0.041
497
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.041
498
SBC016 Subacute Delirium 44 0.041
499
TND004 Tendinopathy 43 0.041
500
MDD018 Middle East Respiratory Syndrome 43 0.041
501
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
502
c BRT038 Baraitser-Winter Syndrome 1 41 0.041
503
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.041
504
CRN322 Coronavirus Infectious Disease 40 0.041
505
P MLG074 Malignant Mesenchymoma 40 0.041
506
HYP540 Hypertension, Diastolic 40 0.041
507
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.041
508
CRN020 Coronary Restenosis 39 0.041
509
HYP344 Hyperthyroidism, Familial Gestational 39 0.041
510
SCR011 Scrapie 39 0.041
511
ADR022 Adrenomyeloneuropathy 38 0.041
512
ATM052 Autoimmune Disease 1 37 0.041
513
c WLM011 Wilms Tumor 6 37 0.041
514
HRW001 Hair Whorl 36 0.041
516
PRG090 Progressive Relapsing Multiple Sclerosis 34 0.041
517
c RNG020 Ring Chromosome 4 33 0.041
518
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.041
519
CHN019 Chand Syndrome 32 0.041
520
DMN026 Dementia Pugilistica 27 0.041
521
HRP008 Herpes Simiae 25 0.041
522
c PSD047 Pseudo-Turner Syndrome 21 0.041
524
ESP021 Esophageal Cancer 90 0.033
525
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.033
527
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.033
528
END057 Endometrial Cancer 74 0.033
529
ULC004 Ulcerative Colitis 73 0.033
530
P FML018 Familial Mediterranean Fever 73 0.033
531
ANX010 Anxiety 73 0.033
532
P ATS364 Autism 70 0.033
533
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.033
534
ADN011 Adenoid Cystic Carcinoma 70 0.033
535
P INF038 Influenza 68 0.033
536
BRK010 Burkitt Lymphoma 67 0.033
537
ALL003 Allergic Rhinitis 67 0.033
538
P BLD062 Bile Duct Cancer 67 0.033
539
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.033
540
P SKN015 Skin Carcinoma 66 0.033
541
P NSP012 Nasopharyngeal Carcinoma 66 0.033
542
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.033
543
P THY023 Thymoma 65 0.033
544
LYS012 Lysosomal Acid Lipase Deficiency 65 0.033
545
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.033
546
c DPH024 Diaphragmatic Hernia, Congenital 63 0.033
547
P ART023 Arthropathy 62 0.033
548
P HMN010 Hemangioma 61 0.033
549
P KDN017 Kidney Cancer 60 0.033
550
P TXP001 Toxoplasmosis 60 0.033
551
STT001 Status Epilepticus 60 0.033
552
P MYC008 Myocarditis 59 0.033
553
P CYS018 Cystitis 59 0.033
554
BRN002 Bronchiolitis 59 0.033
555
GST045 Gastroenteritis 59 0.033
556
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.033
557
P RHN004 Rhinitis 57 0.033
558
P PRN023 Prion Disease 57 0.033
559
c MST023 Mesothelioma, Malignant 57 0.033
560
P ANG015 Angioedema 57 0.033
561
P PLY018 Polycythemia 56 0.033
562
c ACT134 Acute Liver Failure 56 0.033
563
HMG005 Hemoglobinopathy 56 0.033
564
BRN012 Bronchiolitis Obliterans 55 0.033
565
P CRB154 Cerebrocostomandibular Syndrome 55 0.033
566
c BCT007 Bacterial Meningitis 55 0.033
567
P DBT005 Diabetes Insipidus 55 0.033
568
GST037 Gastroparesis 54 0.033
569
P LTR001 Lateral Sclerosis 54 0.033
570
MYM001 Myoma 54 0.033
571
P HMC002 Homocystinuria 53 0.033
572
LYS002 Lysosomal Storage Disease 52 0.033
573
PRP016 Paraplegia 52 0.033
574
ACR041 Acromelic Frontonasal Dysostosis 52 0.033
575
c THY107 Thymoma, Familial 52 0.033
576
HYP088 Hyper-Igd Syndrome 52 0.033
577
P OVR049 Ovarian Disease 52 0.033
578
ILS001 Ileus 51 0.033
579
P CPL006 Capillary Hemangioma 51 0.033
580
P PRC012 Pericardial Effusion 51 0.033
581
P THR015 Thrombophilia 51 0.033
582
P AST007 Astrocytoma 51 0.033
583
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.033
584
HYP781 Hypoascorbemia 51 0.033
585
FSC004 Fasciitis 50 0.033
586
STM007 Stomatitis 50 0.033
587
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.033
588
P OBS001 Obstructive Jaundice 50 0.033
589
SYS003 Systolic Heart Failure 49 0.033
590
CVR006 Cavernous Hemangioma 49 0.033
591
PRS129 Prostatic Hyperplasia, Benign 49 0.033
592
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.033
593
P RNV001 Renovascular Hypertension 48 0.033
594
HMP001 Hemopericardium 48 0.033
595
CHL056 Cheilitis 48 0.033
596
ESN015 Eosinophilic Fasciitis 48 0.033
597
P BNG032 Benign Mesothelioma 46 0.033
598
c MLG068 Malignant Glioma 46 0.033
599
RTR008 Root Resorption 45 0.033
600
URT010 Ureteral Obstruction 45 0.033
601
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.033
602
ATN004 Autonomic Neuropathy 45 0.033
603
P PRL003 Proliferative Glomerulonephritis 44 0.033
604
TRP009 Triple X Syndrome 42 0.033
605
ANG049 Angioedema Induced by Ace Inhibitors 40 0.033
606
GLC008 Glucose Metabolism Disease 40 0.033
607
KLD004 Keloid Disorder 40 0.033
608
c OVR114 Ovarian Cancer 1 38 0.033
609
CHR463 Chronic Actinic Dermatitis 37 0.033
610
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 36 0.033
611
INF013 Inferior Myocardial Infarction 33 0.033
612
CND006 Candida Glabrata 32 0.033
613
RSP007 Respiratory Distress Syndrome, Infant 30 0.033
614
CVR010 Cavernous Malformation 30 0.033
615
c CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.033
616
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.033
617
CNT023 Central Nervous System Hemangioma 25 0.033
618
P CRT085 Carotid Intimal Medial Thickness 2 24 0.033
619
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 17 0.033
620
P ATX030 Ataxia-Telangiectasia 82 0.024
621
MLR004 Malaria 81 0.024
622
CRV035 Cervical Cancer 76 0.024
623
P APL001 Aplastic Anemia 74 0.024
624
c HMC039 Hemochromatosis, Type 1 74 0.024
625
c BTT014 Beta-Thalassemia 74 0.024
626
CRH001 Crohn's Disease 74 0.024
627
P FML011 Familial Adenomatous Polyposis 72 0.024
628
P GRF003 Graft-Versus-Host Disease 72 0.024
629
c LKM063 Leukemia, Chronic Myeloid 72 0.024
630
P PHC003 Pheochromocytoma 71 0.024
631
P MTC003 Metachromatic Leukodystrophy 70 0.024
632
P AMY004 Amyloidosis 70 0.024
633
P HYP061 Hypertrophic Cardiomyopathy 70 0.024
634
P FRG001 Fragile X Syndrome 70 0.024
635
P ASP006 Aspergillosis 69 0.024
636
PLY001 Polycythemia Vera 69 0.024
637
PLM001 Pulmonary Tuberculosis 69 0.024
638
SVR097 Severe Cutaneous Adverse Reaction 69 0.024
639
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.024
640
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.024
641
P ANG001 Angelman Syndrome 69 0.024
642
P LYM118 Lymphoma 68 0.024
643
P MYS003 Myasthenia Gravis 68 0.024
644
PNC129 Pancreatic Adenocarcinoma 68 0.024
645
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.024
646
GST092 Gastroesophageal Reflux 67 0.024
647
P MLG056 Malignant Hyperthermia 67 0.024
648
P MNN013 Meningitis 66 0.024
649
MVL001 Mevalonic Aciduria 66 0.024
650
TTN003 Tetanus 65 0.024
651
P CNJ013 Conjunctivitis 65 0.024
652
BRR014 Barrett Esophagus 65 0.024
653
c JVN010 Juvenile Rheumatoid Arthritis 64 0.024
654
BRC012 Brucellosis 64 0.024
655
LSH001 Leishmaniasis 63 0.024
656
SKN016 Skin Disease 63 0.024
657
ACT119 Acute Promyelocytic Leukemia 63 0.024
658
c ATM011 Autoimmune Hepatitis 63 0.024
659
c OPT053 Optic Atrophy 1 63 0.024
660
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.024
661
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.024
662
HSH003 Hashimoto Thyroiditis 62 0.024
663
CTN007 Cutaneous Leishmaniasis 62 0.024
664
MDD011 Mood Disorder 62 0.024
666
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.024
667
c LPM012 Lipomatosis, Multiple 60 0.024
668
c JVN061 Juvenile Arthritis 60 0.024
669
P BNG030 Benign Ependymoma 60 0.024
670
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.024
671
CRD223 Cardiac Arrhythmia 60 0.024
672
INS001 Insulinoma 60 0.024
673
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.024
674
P THL005 Thalassemia 60 0.024
675
c HRD002 Hereditary Angioedema 60 0.024
676
P LKD001 Leukodystrophy 59 0.024
677
P BRN022 Bronchiectasis 59 0.024
678
THY029 Thyroid Carcinoma 59 0.024
679
SPN027 Spinal Stenosis 59 0.024
680
P BRS044 Breast Adenocarcinoma 59 0.024
681
GNG013 Gingivitis 59 0.024
682
HLC007 Helicobacter Pylori Infection 59 0.024
683
CMP010 Complex Regional Pain Syndrome 58 0.024
684
ADR005 Adrenal Carcinoma 58 0.024
685
ERY003 Erythema Multiforme 58 0.024
686
P URT039 Urticaria 58 0.024
687
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.024
688
P BNC003 Bone Cancer 58 0.024
689
P GLL018 Gallbladder Cancer 57 0.024
690
BRN056 Bronchopulmonary Dysplasia 57 0.024
691
c VSC019 Vesicoureteral Reflux 1 57 0.024
692
DSS009 Disseminated Intravascular Coagulation 57 0.024
693
SCH014 Schistosomiasis 57 0.024
694
PHR003 Pharyngitis 57 0.024
695
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.024
696
LST001 Listeriosis 56 0.024
697
GNR004 Generalized Anxiety Disorder 56 0.024
698
P PNM006 Pneumoconiosis 56 0.024
699
c NPH055 Nephrotic Syndrome, Type 1 56 0.024
700
P GST044 Gastritis 56 0.024
701
ATR057 Atrioventricular Block 55 0.024
702
CHR100 Chronic Ulcer of Skin 55 0.024
703
HMP005 Hemiplegia 55 0.024
704
HRY003 Hairy Cell Leukemia 55 0.024
705
SYN007 Synovitis 54 0.024
706
AMN003 Amnestic Disorder 54 0.024
707
CLL010 Cellular Ependymoma 54 0.024
708
AMN001 Amenorrhea 54 0.024
709
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.024
710
P LCH002 Lichen Planus 53 0.024
711
P END047 Endophthalmitis 53 0.024
712
FRZ001 Frozen Shoulder 53 0.024
713
P CTN003 Cutaneous Lupus Erythematosus 53 0.024
714
CLF001 Cleft Lip 53 0.024
715
GTR002 Goiter 53 0.024
716
P PTS002 Ptosis 53 0.024
717
INT075 Intracranial Hypertension 53 0.024
718
P MSC003 Muscular Atrophy 52 0.024
719
P THY032 Thyroiditis 52 0.024
720
HYP014 Hyperuricemia 52 0.024
721
TLN003 Telangiectasis 52 0.024
722
c ACT135 Acute Graft Versus Host Disease 52 0.024
723
c VRL005 Viral Pneumonia 52 0.024
724
THR004 Thrombocytosis 51 0.024
726
ANK001 Ankylosis 51 0.024
727
TNG007 Tongue Carcinoma 51 0.024
728
P PST095 Post-Thrombotic Syndrome 51 0.024
729
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.024
730
P MMB011 Membranous Nephropathy 50 0.024
731
PLR008 Pleurisy 50 0.024
732
c PYR010 Peyronie's Disease 50 0.024
733
P ECL001 Eclampsia 50 0.024
734
DDN011 Duodenal Atresia 50 0.024
735
P ESN008 Eosinophilic Pneumonia 50 0.024
736
AZS001 Azoospermia 50 0.024
737
MCP006 Mucoepidermoid Carcinoma 50 0.024
738
P TMP001 Temporal Lobe Epilepsy 50 0.024
739
P AGG001 Aggressive Periodontitis 50 0.024
740
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.024
741
HMG002 Hemoglobinuria 50 0.024
742
ILT001 Ileitis 50 0.024
743
DYS073 Dysphagia 50 0.024
744
c INF023 Inflammatory Breast Carcinoma 50 0.024
745
P ATR005 Atrophic Gastritis 50 0.024
746
P MTC133 Mitochondrial Myopathy 49 0.024
747
P ART018 Aortic Valve Insufficiency 49 0.024
748
BNG036 Bone Giant Cell Tumor 49 0.024
749
CHL004 Cholelithiasis 49 0.024
750
P CTN015 Cutaneous T Cell Lymphoma 49 0.024
751
ATS010 Autosomal Recessive Disease 48 0.024
752
BRS064 Bursitis 48 0.024
753
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.024
754
c NPH049 Nephrotic Syndrome, Type 2 48 0.024
755
VTM033 Vitamin K Deficiency Bleeding 48 0.024
756
c MTR002 Mitral Valve Insufficiency 48 0.024
757
HYP025 Hyperphosphatemia 48 0.024
758
INT010 Intracranial Embolism 48 0.024
759
ANT018 Anthracosis 48 0.024
760
P DPY001 Dupuytren Contracture 48 0.024
761
HLX001 Helix Syndrome 47 0.024
762
GRM005 Germ Cell Cancer 47 0.024
763
P RNL015 Renal Hypertension 47 0.024
764
P ERY008 Erythromelalgia 47 0.024
765
c CRB191 Cerebral Cavernous Malformations 2 47 0.024
766
CNZ001 Coenzyme Q10 Deficiency Disease 47 0.024
767
TST044 Testicular Torsion 47 0.024
768
CRD137 Cardiogenic Shock 47 0.024
769
CHR074 Choriocarcinoma 47 0.024
770
ATN005 Autonomic Dysfunction 46 0.024
771
MYC005 Myocardial Stunning 46 0.024
772
FLL008 Folliculitis 46 0.024
773
ADR040 Adrenal Gland Pheochromocytoma 46 0.024
774
HMR023 Hemorrhagic Cystitis 45 0.024
775
PRT019 Protein-Losing Enteropathy 45 0.024
776
P END084 Endocrine System Disease 45 0.024
777
P RPP006 Rippling Muscle Disease 2 44 0.024
778
PRT035 Peritoneum Cancer 44 0.024
779
PPL001 Papillary Adenoma 44 0.024
780
BCT021 Bacterial Sepsis 44 0.024
781
P TST026 Testicular Germ Cell Cancer 43 0.024
782
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.024
783
TST015 Testicular Disease 43 0.024
784
MCR011 Microinvasive Gastric Cancer 43 0.024
785
NSP002 Nasopharyngitis 43 0.024
786
P MLT008 Multinodular Goiter 42 0.024
787
P AVS003 Avascular Necrosis 42 0.024
788
PNM013 Pneumococcal Meningitis 42 0.024
789
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.024
790
MNN017 Mononeuropathy 42 0.024
791
OBS082 Obstructive Nephropathy 42 0.024
792
SKN023 Skin Tag 42 0.024
793
TND006 Tendinosis 42 0.024
794
ANC002 Anca-Associated Vasculitis 41 0.024
795
DNT006 Dental Pulp Necrosis 41 0.024
796
P KLZ004 Kala-Azar 1 41 0.024
797
MRP001 Morphine Dependence 41 0.024
798
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.024
799
OST115 Osteonecrosis of the Jaw 40 0.024
800
ANX004 Anoxia 40 0.024
801
PLM005 Pleomorphic Lipoma 40 0.024
802
WLL004 Wallerian Degeneration 39 0.024
803
FLL031 Follicular Adenoma 39 0.024
804
CHL070 Cholesterol Embolism 39 0.024
805
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.024
806
TRC005 Tracheal Stenosis 38 0.024
807
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.024
808
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.024
809
STR077 Streptococcal Toxic-Shock Syndrome 37 0.024
810
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.024
811
ATN021 Autoinflammatory Syndrome 36 0.024
812
BRR002 Barrett's Adenocarcinoma 36 0.024
813
PLC002 Plica Syndrome 36 0.024
814
CHR178 Chromosomal Triplication 35 0.024
815
LNG091 Lung Mucoepidermoid Carcinoma 35 0.024
816
XNT009 Xanthoma Disseminatum 34 0.024
817
AMR003 Amaurosis Fugax 34 0.024
818
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.024
819
LCH013 Lichen Planus Pemphigoides 34 0.024
820
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.024
821
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.024
822
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.024
823
P HRD022 Hordeolum 31 0.024
824
PLY150 Polykaryocytosis Inducer 31 0.024
825
ALV001 Alveolar Periostitis 30 0.024
826
ERY066 Erythema Multiforme Major 30 0.024
827
c ATM100 Autoimmune Optic Neuritis 30 0.024
828
MRL006 Meralgia Paraesthetica, Familial 29 0.024
829
DFF010 Diffuse Alopecia Areata 26 0.024
830
DFC001 Defective Apolipoprotein B-100 26 0.024
831
ADG002 Audiogenic Seizures 25 0.024
832
c PRM243 Primary Bone Cancer 24 0.024
833
DRG016 Drug Induced Dyskinesia 24 0.024
834
c RNG021 Ring Chromosome 5 23 0.024
835
HML018 Homologous Wasting Disease 22 0.024
836
CD4008 Cd4/cd8 T-Cell Ratio 20 0.024
837
ODN022 Odontoid Hypoplasia 18 0.024
838
IDP022 Idiopathic Spinal Cord Herniation 17 0.024
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