Search results for Simvastatin

1042 hits were found for Simvastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 58 0.244
2
P HYP607 Hypercholesterolemia, Familial 76 0.194
3
P FML035 Familial Hyperlipidemia 48 0.192
4
END072 Endotheliitis 42 0.152
5
ATH003 Atherosclerosis 65 0.146
6
P HRT032 Heart Disease 75 0.140
7
P CRN211 Coronary Artery Disease 74 0.137
8
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.126
9
PRP027 Peripheral Vascular Disease 68 0.125
10
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.121
11
ISC006 Ischemic Heart Disease 68 0.119
12
ART111 Artery Disease 55 0.118
13
c HYP333 Hyperlipidemia, Combined, 2 15 0.116
14
ART021 Arteriosclerosis 58 0.108
15
P HYP117 Hypertriglyceridemia 61 0.104
16
c CRN175 Coronary Heart Disease 4 19 0.104
17
c CRN172 Coronary Heart Disease 3 19 0.104
18
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.102
19
GLC008 Glucose Metabolism Disease 42 0.102
20
MDY003 Mody, Type Ii 36 0.100
21
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.096
22
STT044 Statin Toxicity 14 0.094
23
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.092
24
P CRN178 Coronary Heart Disease 6 21 0.092
25
c HYP595 Hypertension, Essential 69 0.089
26
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.089
27
c CRN174 Coronary Heart Disease 2 20 0.089
28
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.087
29
ISC004 Ischemia 61 0.087
30
c HYP163 Hyperlipidemia Type 3 36 0.087
31
ADL002 Adult Syndrome 52 0.084
32
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.084
33
VSC007 Vascular Disease 67 0.082
34
CRD118 Cardiovascular Cancer 44 0.082
35
P MYC007 Myocardial Infarction 79 0.079
36
BLD054 Blood Protein Disease 37 0.079
37
P LVR013 Liver Disease 75 0.077
38
P HPT021 Hepatitis 69 0.077
39
CRB039 Cerebrovascular Disease 63 0.077
40
P PRD008 Periodontitis 63 0.074
41
P GST049 Gastrointestinal System Cancer 60 0.074
42
ATM052 Autoimmune Disease 1 25 0.074
43
c CRN214 Coronary Heart Disease 5 22 0.074
44
ATM053 Autoimmune Disease 2 16 0.074
45
P CLR023 Colorectal Cancer 97 0.071
46
ANR040 Aneurysm 57 0.071
47
VSC006 Vascular Cancer 51 0.071
48
P HYP614 Hyperlipidemia, Familial Combined 50 0.071
49
CSY001 C Syndrome 50 0.071
50
VTM003 Vitamin Metabolic Disorder 30 0.071
51
P RHM011 Rheumatoid Arthritis 89 0.068
52
P ART022 Arthritis 75 0.068
53
PRT036 Peritonitis 63 0.068
54
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.068
55
PLS009 Plasma Cell Neoplasm 48 0.068
56
TYP027 Type 1 Diabetes Mellitus 10 27 0.068
57
SMT004 Smith-Lemli-Opitz Syndrome 66 0.065
58
P KDN018 Kidney Disease 66 0.065
59
MTH009 Mouth Disease 61 0.065
60
P HYP060 Hyperinsulinism 58 0.065
61
INT253 Intestinal Benign Neoplasm 47 0.065
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.065
63
PRP080 Peripheral Artery Disease 37 0.065
64
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.065
65
P BRS047 Breast Cancer 100 0.061
66
P LNG032 Lung Cancer 95 0.061
67
P MLT019 Multiple Myeloma 83 0.061
68
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.061
69
LVR012 Liver Cirrhosis 67 0.061
70
P MYP004 Myopathy 67 0.061
71
P PLY011 Polycystic Ovary Syndrome 65 0.061
72
c ACT075 Acute Myocardial Infarction 60 0.061
73
P PRT013 Portal Hypertension 60 0.061
74
CRT016 Carotid Artery Disease 57 0.061
75
RCT018 Rectal Neoplasm 54 0.061
76
BRN038 Bronchial Disease 51 0.061
77
CLN019 Colonic Disease 51 0.061
78
P BLD051 Blood Coagulation Disease 42 0.061
79
RCT017 Rectal Disease 40 0.061
80
c CLR079 Colorectal Cancer 2 29 0.061
81
LNG099 Lung Disease 64 0.058
82
CNN005 Connective Tissue Disease 62 0.058
83
P PNC044 Pancreatitis 61 0.058
84
RSP006 Respiratory System Disease 58 0.058
85
CTS003 Coats Disease 57 0.058
86
P HMR003 Hemorrhagic Disease 57 0.058
87
GST050 Gastrointestinal System Disease 56 0.058
88
TTH006 Tooth Disease 52 0.058
89
BLD053 Blood Platelet Disease 46 0.058
90
ALN001 Aland Island Eye Disease 45 0.058
91
CRT015 Carotid Artery Occlusion 43 0.058
92
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.058
93
HPT020 Hepatic Vascular Disease 42 0.058
94
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.058
95
RPR002 Reproductive System Disease 41 0.058
96
c HYP272 Hypercholesterolemia, Familial, 3 32 0.058
97
P OBS005 Obesity 92 0.054
98
P PLM037 Pulmonary Hypertension 79 0.054
99
P OVR042 Ovarian Cancer 76 0.054
100
P LPS004 Lupus Erythematosus 64 0.054
101
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.054
102
DMY004 Demyelinating Disease 53 0.054
103
ALL026 Allergic Hypersensitivity Disease 52 0.054
104
FML038 Female Reproductive Organ Cancer 50 0.054
105
c INH020 Inherited Metabolic Disorder 49 0.054
106
FML039 Female Reproductive System Disease 48 0.054
107
CRB025 Carbohydrate Metabolic Disorder 46 0.054
108
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.054
109
IMP003 Impaired Renal Function Disease 34 0.054
110
PLS010 Plasma Protein Metabolism Disease 34 0.054
111
VSC008 Vascular Hemostatic Disease 30 0.054
112
c MLT094 Multiple Sclerosis 3 24 0.054
113
ATM059 Autoimmune Disease 6 22 0.054
114
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.054
115
c CRN177 Coronary Heart Disease 7 20 0.054
116
c MLT093 Multiple Sclerosis 2 18 0.054
117
ATM054 Autoimmune Disease 3 15 0.054
118
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.054
119
P PNC035 Pancreatic Cancer 87 0.050
120
c SYS001 Systemic Lupus Erythematosus 86 0.050
121
STR067 Stroke, Ischemic 75 0.050
122
P ADN016 Adenocarcinoma 69 0.050
123
c CHR089 Chronic Kidney Failure 66 0.050
124
DMN002 Dementia 65 0.050
125
P PLR004 Pleuropulmonary Blastoma 65 0.050
126
HYP066 Hyperglycemia 61 0.050
127
P INT068 Intestinal Disease 60 0.050
128
PRD007 Periodontal Disease 60 0.050
129
P ENC018 Encephalopathy 59 0.050
130
P INF032 Infertility 59 0.050
131
WLL006 Wells Syndrome 59 0.050
132
ALP008 Alopecia 57 0.050
133
PLY023 Polycystic Liver Disease 56 0.050
134
P OVR049 Ovarian Disease 56 0.050
135
END030 End Stage Renal Failure 55 0.050
136
DSS008 Disease of Mental Health 52 0.050
137
BRN071 Brain Injury 52 0.050
138
P OVR046 Ovarian Cyst 51 0.050
139
STM006 Stomach Disease 50 0.050
140
URN009 Urinary System Disease 50 0.050
141
P URF003 Urofacial Syndrome 1 50 0.050
142
c HMG001 Hemoglobin C Disease 47 0.050
143
VND001 Vein Disease 47 0.050
144
CRB085 Cerebral Hemorrhage 46 0.050
145
INC022 Inclusion-Cell Disease 46 0.050
146
c CLL013 Cell Type Cancer 46 0.050
147
ACD009 Acid-Labile Subunit, Deficiency of 45 0.050
148
GDS001 Good Syndrome 44 0.050
149
P BRN120 Bronchus Cancer 44 0.050
150
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.050
151
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.050
152
CRB009 Cerebritis 39 0.050
153
GND003 Gonadal Disease 39 0.050
154
P OCY001 Oocyte Maturation Defect 38 0.050
155
MLR007 Male Reproductive System Disease 34 0.050
156
c CLR075 Colorectal Cancer 3 28 0.050
157
c PLY105 Polycystic Ovary Syndrome 1 21 0.050
158
RFR001 Refractory Plasma Cell Neoplasm 16 0.050
159
P HPT023 Hepatocellular Carcinoma 92 0.046
160
P PRS040 Prostate Cancer 90 0.046
161
P AST005 Asthma 82 0.046
162
P LKM002 Leukemia 71 0.046
163
SKN016 Skin Disease 66 0.046
164
P ALP009 Alopecia Areata 62 0.046
165
c HPT003 Hepatitis a 59 0.046
166
P NPH012 Nephrotic Syndrome 59 0.046
167
PNC034 Pancreas Disease 58 0.046
168
CHL071 Child Syndrome 58 0.046
169
P INT070 Intestinal Obstruction 57 0.046
170
P SML001 Small Cell Carcinoma 56 0.046
171
PLN006 Poland Syndrome 54 0.046
172
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.046
173
SML033 Small Cell Cancer of the Lung, Somatic 54 0.046
174
TRM010 Traumatic Brain Injury 52 0.046
175
NRT004 Neuritis 52 0.046
176
OPT009 Optic Neuritis 50 0.046
177
GNG011 Gingival Disease 46 0.046
178
SKN023 Skin Tag 44 0.046
179
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.046
180
BRN080 Brain Ischemia 41 0.046
181
SPN369 Spinal Disease 39 0.046
182
HYP540 Hypertension, Diastolic 39 0.046
183
c PNC106 Pancreatic Agenesis 1 37 0.046
184
ATM014 Autoimmune Disease of Endocrine System 36 0.046
185
ALR002 Al-Raqad Syndrome 36 0.046
186
MDY004 Mody, Type Iii 34 0.046
187
ACD004 Acdc 33 0.046
188
c CLR080 Colorectal Cancer 5 32 0.046
189
CVT001 Cavitary Optic Disc Anomalies 31 0.046
190
c HMG004 Hemoglobin D Disease 31 0.046
191
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.046
192
PRM243 Primary Bone Cancer 29 0.046
193
c AST037 Asthma 1 28 0.046
194
RFR004 Refractory Hematologic Cancer 28 0.046
195
c SYS055 Systemic Lupus Erythematosus 12 20 0.046
196
c MLT095 Multiple Sclerosis 4 16 0.046
197
ATM055 Autoimmune Disease 4 15 0.046
198
P ALZ034 Alzheimer Disease 92 0.041
199
GST053 Gastric Cancer 78 0.041
200
CNG034 Congestive Heart Failure 72 0.041
201
P PLM036 Pulmonary Fibrosis 71 0.041
202
P PNM007 Pneumonia 68 0.041
203
P CLC005 Celiac Disease 68 0.041
204
PSY004 Psychotic Disorder 67 0.041
205
P LYM007 Lymphangioleiomyomatosis 66 0.041
206
ATP002 Atopy 66 0.041
207
c HPT016 Hepatitis B 64 0.041
208
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.041
209
EYD002 Eye Disease 61 0.041
210
RBR001 Roberts Syndrome 60 0.041
211
OCL009 Ocular Cancer 59 0.041
212
RHM027 Rheumatic Disease 58 0.041
213
ETH011 Ethylmalonic Encephalopathy 56 0.041
214
INT002 Intermittent Claudication 56 0.041
215
GLC003 Glucose Intolerance 55 0.041
216
KDS001 Kid Syndrome 53 0.041
217
c HPT015 Hepatitis D 52 0.041
218
P HRD018 Hair Disease 51 0.041
219
ATR060 Atrial Standstill, Digenic 51 0.041
220
FML037 Female Breast Cancer 50 0.041
221
NNL002 Nonalcoholic Steatohepatitis 50 0.041
222
P CLL015 Collagen Disease 50 0.041
223
ANG054 Angina Pectoris 50 0.041
224
MSC072 Muscle Cancer 49 0.041
225
LRN003 Learning Disability 49 0.041
226
NSD001 Nose Disease 48 0.041
227
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.041
228
GLT021 Glutaricaciduria, Type I 46 0.041
229
ACR041 Acromelic Frontonasal Dysostosis 45 0.041
230
c MTR002 Mitral Valve Insufficiency 44 0.041
231
BRT030 Birth Defects 43 0.041
232
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.041
233
MLR006 Male Reproductive Organ Cancer 43 0.041
234
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.041
235
LKC003 Leukocyte Disease 43 0.041
236
BLR008 Bilirubin Metabolic Disorder 42 0.041
237
PRM025 Primary Bacterial Infectious Disease 41 0.041
238
NRN002 Neuronitis 41 0.041
239
P CNN004 Connective Tissue Cancer 40 0.041
240
CRB086 Cerebral Aneurysms 39 0.041
241
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.041
242
MNR003 Mineral Metabolism Disease 38 0.041
243
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 37 0.041
244
BNS002 Bone Structure Disease 37 0.041
245
NSY001 N Syndrome 36 0.041
246
INF013 Inferior Myocardial Infarction 35 0.041
247
PNL013 Penile Disease 34 0.041
248
MSC004 Muscle Tissue Disease 34 0.041
249
P XLN007 X-Linked Disease 34 0.041
250
c SYS043 Systemic Lupus Erythematosus 1 33 0.041
251
GLB003 Globe Disease 32 0.041
252
c CNN010 Connective Tissue Benign Neoplasm 32 0.041
253
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 32 0.041
254
MDY005 Mody, Type I 30 0.041
255
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 30 0.041
256
IRN007 Irinotecan Toxicity 30 0.041
257
c MYC058 Myocardial Infarction 2 28 0.041
258
c SYS040 Systemic Lupus Erythematosus 10 22 0.041
259
c DBT053 Diabetes Mellitus, Insulin-Dependent, 23 21 0.041
260
c CRN173 Coronary Heart Disease 8 18 0.041
261
c CLR078 Colorectal Cancer 11 17 0.041
262
c SML023 Small Cell Lung Cancer, Adult 15 0.041
263
CYS001 Cystic Fibrosis 83 0.035
264
P HNT016 Huntington Disease 80 0.035
265
P SCH015 Schizophrenia 77 0.035
266
ADR007 Adrenoleukodystrophy 72 0.035
267
SCK003 Sickle Cell Anemia 71 0.035
268
P RSP003 Respiratory Failure 71 0.035
269
BRN028 Brain Cancer 70 0.035
270
CRZ001 Crouzon Syndrome 70 0.035
271
P LYM118 Lymphoma 69 0.035
272
c HPT001 Hepatitis C 68 0.035
273
P TBR001 Tuberous Sclerosis 67 0.035
274
P END044 Endometriosis 66 0.035
275
P ATR011 Atrial Fibrillation 66 0.035
276
P EPL164 Epilepsy 66 0.035
277
c BSL007 Basal Cell Carcinoma 65 0.035
278
CNT098 Central Core Disease 65 0.035
279
P AMY004 Amyloidosis 65 0.035
280
P ART023 Arthropathy 64 0.035
281
DFC004 Deficiency Anemia 64 0.035
282
P HML002 Hemolytic Anemia 62 0.035
283
P DRM010 Dermatomyositis 62 0.035
284
CRB011 Cerebrotendinous Xanthomatosis 61 0.035
285
BRS051 Breast Disease 61 0.035
286
P GLM045 Glioma 60 0.035
287
P NRV006 Nervous System Cancer 60 0.035
288
c VRL010 Viral Hepatitis 60 0.035
289
c CNT035 Central Nervous System Disease 60 0.035
290
P ORL007 Oral Cavity Cancer 59 0.035
291
FTT001 Fatty Liver Disease 59 0.035
292
P NRP001 Neuropathy 59 0.035
293
ALL006 Allergic Asthma 58 0.035
294
P SHR029 Short Syndrome 58 0.035
295
ADN018 Adenoma 58 0.035
296
P UVT001 Uveitis 58 0.035
297
BNC003 Bone Cancer 58 0.035
298
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.035
299
P HYP040 Hypospadias 57 0.035
300
RHB003 Rhabdomyosarcoma 57 0.035
301
CHY002 Chylomicron Retention Disease 57 0.035
302
UTR039 Uterine Fibroid 57 0.035
303
P MYS005 Myositis 57 0.035
304
ORL011 Oral Cancer 56 0.035
305
P SZR006 Seizure Disorder 56 0.035
306
NRM005 Neuromuscular Disease 56 0.035
307
HYP266 Hypoxia 56 0.035
308
c MYT020 Myotonic Dystrophy 2 56 0.035
309
VRL011 Viral Infectious Disease 55 0.035
310
JNT002 Joint Disorders 55 0.035
311
DBT010 Diabetic Neuropathy 55 0.035
312
PRP019 Peripheral Nervous System Disease 55 0.035
313
PLM034 Pulmonary Emphysema 55 0.035
314
CLF027 Cleft Palate, Isolated 55 0.035
315
c PND001 Pain Disorder 54 0.035
316
P MCR129 Microvascular Complications of Diabetes 1 54 0.035
317
LMY002 Leiomyoma 54 0.035
318
ESP023 Esophageal Disease 54 0.035
319
P INT030 Intracranial Aneurysm 54 0.035
320
c ART101 Aortic Valve Disease 2 53 0.035
321
P MTC069 Mitochondrial Disorders 53 0.035
322
C3D001 C3 Deficiency 53 0.035
323
FRB001 Farber Lipogranulomatosis 53 0.035
324
SLP005 Sleep Disorder 53 0.035
325
AGN012 Agnathia-Otocephaly Complex 53 0.035
326
c INS002 in Situ Carcinoma 53 0.035
327
RTN018 Retinal Disease 53 0.035
328
BRN004 Brain Edema 52 0.035
329
HMG005 Hemoglobinopathy 52 0.035
330
P MSC033 Muscle Disorders 52 0.035
331
OPT006 Optic Nerve Disease 52 0.035
332
PRS042 Prostate Disease 52 0.035
333
IMP005 Impotence 51 0.035
334
P PRM006 Primary Biliary Cirrhosis 51 0.035
335
c BRS049 Breast Carcinoma in Situ 51 0.035
336
DCT002 Ductal Carcinoma in Situ 51 0.035
337
IMM136 Immune System Disease 51 0.035
338
SCK005 Sickle Cell Disease 51 0.035
339
SPN041 Spinal Cord Disease 51 0.035
340
HND003 Hand-Foot-Uterus Syndrome 50 0.035
341
BRS099 Breast Ductal Carcinoma 50 0.035
342
HYP006 Hypertensive Heart Disease 50 0.035
343
MVM001 Movement Disease 49 0.035
344
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.035
345
c ACT071 Acute Kidney Failure 49 0.035
346
MLL012 Miller Syndrome 49 0.035
347
ACT017 Acute Chest Syndrome 48 0.035
348
P RNL015 Renal Hypertension 48 0.035
349
c CNG027 Congenital Hemolytic Anemia 48 0.035
350
HMZ003 Homozygous Familial Hypercholesterolemia 47 0.035
351
HYP043 Hyperandrogenism 47 0.035
352
PRP021 Peripheral Nervous System Neoplasm 46 0.035
353
HRT007 Heart Cancer 46 0.035
354
ADR038 Adermatoglyphia 46 0.035
355
XNT003 Xanthomatosis 46 0.035
356
P CRN074 Coronary Artery Aneurysm 46 0.035
357
c MCR113 Microvascular Complications of Diabetes 3 45 0.035
358
c CLR085 Colorectal Cancer 1 45 0.035
359
VSC047 Vascular Malformation 45 0.035
360
P ABD003 Abdominal Aortic Aneurysm 45 0.035
361
P LYD001 Leydig Cell Tumor 44 0.035
362
DYS018 Dysostosis 44 0.035
363
P SKN013 Skin Benign Neoplasm 43 0.035
364
SKN027 Skin Conditions 43 0.035
365
PRD004 Prediabetes Syndrome 43 0.035
366
GST071 Gastrointestinal Carcinoma 42 0.035
367
ESP002 Esophageal Varix 41 0.035
368
CLV009 Clove Syndrome, Somatic 41 0.035
369
ACT084 Acute Stress Disorder 40 0.035
370
HRT012 Heart Valve Disease 40 0.035
371
P ARC016 Auriculocondylar Syndrome 1 40 0.035
372
BND014 Bone Development Disease 40 0.035
373
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.035
374
CRN020 Coronary Restenosis 39 0.035
375
ACT088 Acute Insulin Response 39 0.035
376
c CLL012 Cell Type Benign Neoplasm 39 0.035
377
P FML187 Familial Hypertension 38 0.035
378
ABR009 Abruzzo-Erickson Syndrome 38 0.035
379
DRG001 Drug Psychosis 38 0.035
380
c SKN012 Skin Carcinoma in Situ 38 0.035
381
c PRS116 Prostate Cancer 1 37 0.035
382
GNR003 Generalized Atherosclerosis 37 0.035
383
NTR005 Nutritional Deficiency Disease 36 0.035
384
MTC005 Mitochondrial Metabolism Disease 36 0.035
385
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.035
386
c BRT038 Baraitser-Winter Syndrome 1 35 0.035
387
ACR002 Acrocapitofemoral Dysplasia 33 0.035
388
LYM023 Lymphatic System Cancer 33 0.035
389
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 32 0.035
390
CRN006 Coronary Aneurysm 32 0.035
391
P HRT017 Heart Tumor 32 0.035
392
FST001 Foster-Kennedy Syndrome 31 0.035
393
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.035
394
MDY006 Mody, Type Iv 30 0.035
395
c OPT051 Opitz Gbbb Syndrome, Type I 30 0.035
396
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.035
397
c AST039 Asthma 2 28 0.035
398
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.035
399
INT053 Intracranial Vasospasm 28 0.035
400
c PNC111 Pancreatic Cancer 2 28 0.035
401
CRB031 Cerebral Arterial Disease 27 0.035
402
HRT006 Heart Aneurysm 24 0.035
403
c SYS051 Systemic Lupus Erythematosus 4 20 0.035
404
UVL003 Uveal Diseases 18 0.035
405
c CRN176 Coronary Heart Disease 9 18 0.035
406
c ADL079 Adult Heart Tumor 16 0.035
407
CLF021 Cleft Palate X-Linked 15 0.035
408
MLG026 Male Genital Organ Vascular Disease 14 0.035
409
ART013 Aortic Malignant Tumor 14 0.035
410
c DLT001 Delta Chain Disease 13 0.035
411
MXL011 Maxillofacial Dysostosis 12 0.035
412
P RNL014 Renal Cell Carcinoma 82 0.029
413
P MDL005 Medulloblastoma 77 0.029
414
HDG012 Hodgkin Lymphoma 77 0.029
415
c CHR090 Chronic Lymphocytic Leukemia 76 0.029
416
P RTN024 Retinoblastoma 74 0.029
417
c HPT073 Hepatitis C Virus 73 0.029
418
WLS001 Wilson Disease 72 0.029
419
P NRV007 Nervous System Disease 71 0.029
420
MLT021 Multiple System Atrophy 70 0.029
421
P PRK057 Parkinson Disease, Late-Onset 70 0.029
422
P NRB001 Neuroblastoma 70 0.029
423
TST021 Testicular Germ Cell Tumor 69 0.029
424
c MLT136 Multiple Endocrine Neoplasia 1 69 0.029
425
ART016 Aortic Aneurysm 69 0.029
426
P CRD011 Cardiomyopathy 68 0.029
427
WRN001 Werner Syndrome 67 0.029
428
EWN003 Ewing Sarcoma 66 0.029
429
URN008 Urinary Bladder Cancer 66 0.029
430
DRM006 Dermatitis 66 0.029
431
SRC014 Sarcoma 66 0.029
432
P KDN017 Kidney Cancer 65 0.029
433
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.029
434
HMT002 Hematologic Cancer 64 0.029
435
BRN024 Bronchitis 64 0.029
436
P HYP086 Hypothyroidism 64 0.029
437
P OST002 Osteoporosis 64 0.029
438
P INF037 Inflammatory Bowel Disease 63 0.029
439
WLM007 Wilms Tumor Susceptibility-5 63 0.029
440
ALC007 Alcohol Dependence 63 0.029
441
RNL101 Renal Cell Carcinoma, Papillary 63 0.029
442
OST085 Osteosarcoma, Somatic 63 0.029
443
c TBR024 Tuberous Sclerosis-1 63 0.029
444
SPN186 Spinal Cord Injury 63 0.029
445
MLN008 Melanoma 62 0.029
446
P MCL013 Mucolipidosis Iv 62 0.029
447
P LNG064 Lung Cancer Susceptibility 3 62 0.029
448
P ADD001 Addison's Disease 62 0.029
449
MXD005 Mixed Connective Tissue Disease 62 0.029
450
P BPL003 Bipolar Disorder 62 0.029
451
P LYM026 Lymphoblastic Leukemia 62 0.029
452
HYP056 Hypoglycemia 61 0.029
453
VNW001 Von Willebrand's Disease 61 0.029
454
CRD119 Cardiac Arrest 61 0.029
455
P RCK004 Rickets 61 0.029
456
P SNS014 Sinusitis 60 0.029
457
TXC005 Toxic Shock Syndrome 60 0.029
458
PRM097 Primary Immunodeficiency Disease 60 0.029
459
WLL001 Williams-Beuren Syndrome 60 0.029
460
c ATM011 Autoimmune Hepatitis 60 0.029
461
P DRR001 Diarrhea 60 0.029
462
P GRV001 Graves' Disease 59 0.029
463
P GLM007 Glomerulonephritis 59 0.029
464
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.029
465
P CTR002 Cataract 58 0.029
466
P MSC007 Muscle Hypertrophy 58 0.029
467
c PNC108 Pancreatitis, Hereditary 58 0.029
468
P WLD002 Waldenstrom Macroglobulinemia 58 0.029
469
ABL002 Ablepharon-Macrostomia Syndrome 57 0.029
470
EMB004 Embryonal Carcinoma 57 0.029
471
ART017 Aortic Disease 57 0.029
472
c CWD006 Cowden Syndrome 1 57 0.029
473
SFT003 Soft Tissue Sarcoma 57 0.029
474
MSC077 Muscle Eye Brain Disease 57 0.029
475
c ACT027 Acute Pancreatitis 57 0.029
476
EXF001 Exfoliation Syndrome 57 0.029
477
WST001 West Syndrome 57 0.029
478
TRN015 Transient Cerebral Ischemia 56 0.029
479
P MLT074 Multiple Endocrine Neoplasia 56 0.029
480
P LYM033 Lymphoproliferative Syndrome 56 0.029
481
P PLY019 Polyneuropathy 56 0.029
482
CLR003 Clear Cell Adenocarcinoma 56 0.029
483
PRS047 Prostatitis 56 0.029
484
P HYP076 Hyperthyroidism 55 0.029
485
MLN007 Male Infertility 55 0.029
486
HPT022 Hepatoblastoma 55 0.029
487
c THR092 Thrombophilia Due to Thrombin Defect 54 0.029
488
P EMB005 Embryonal Rhabdomyosarcoma 54 0.029
489
P NLD001 Nail Disease 54 0.029
490
P MMB011 Membranous Nephropathy 54 0.029
491
P THY032 Thyroiditis 54 0.029
492
VSC002 Vascular Dementia 54 0.029
493
c RNL003 Renal Clear Cell Carcinoma 54 0.029
494
RHM001 Rheumatic Fever 54 0.029
495
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.029
496
CHR081 Choroideremia 54 0.029
497
NWC001 Newcastle Disease 54 0.029
498
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 54 0.029
499
CND002 Conduct Disorder 54 0.029
500
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.029
501
TRN018 Transitional Cell Carcinoma 53 0.029
502
P PLY014 Polycystic Kidney Disease 53 0.029
503
P EXP004 Exophthalmos 53 0.029
504
END040 Endogenous Depression 53 0.029
505
CLR030 Clear Cell Renal Cell Carcinoma 53 0.029
506
P CNT005 Central Nervous System Lymphoma 53 0.029
507
LYM019 Lymphosarcoma 53 0.029
508
HMR039 Hemorrhage, Intracerebral 53 0.029
509
MNT002 Mental Depression 53 0.029
510
GTR002 Goiter 52 0.029
511
BLM002 Bulimia Nervosa 52 0.029
512
KRT002 Keratomalacia 52 0.029
513
ECT006 Ectodermal Dysplasia 52 0.029
514
P SPS003 Spastic Diplegia 52 0.029
515
KRT009 Keratosis 52 0.029
516
LYM024 Lymphatic System Disease 52 0.029
517
ATY005 Atypical Teratoid Rhabdoid Tumor 52 0.029
518
DBT004 Diabetic Polyneuropathy 52 0.029
519
c PRK031 Parkinson Disease 1 51 0.029
520
BLD044 Bladder Disease 51 0.029
521
P GND004 Gonadal Dysgenesis 51 0.029
522
CLR109 Colorectal Adenocarcinoma 51 0.029
523
GNR004 Generalized Anxiety Disorder 51 0.029
524
CRN030 Coronary Stenosis 51 0.029
525
BLD131 Bladder Urothelial Carcinoma 51 0.029
526
INT007 Intermediate Coronary Syndrome 50 0.029
527
CLN015 Colon Adenocarcinoma 50 0.029
528
CLC006 Calcinosis 50 0.029
529
RTN023 Retinitis 50 0.029
530
MST017 Mast Cell Disease 50 0.029
531
MCR004 Macroglobulinemia 50 0.029
532
P CHR345 Chronic Pain 50 0.029
533
PRL032 Perlman Syndrome 50 0.029
534
c LYM107 Lymphoproliferative Syndrome 2 50 0.029
535
RHB001 Rhabdoid Cancer 50 0.029
536
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.029
537
RHM028 Rheumatic Heart Disease 50 0.029
538
DRG003 Drug Dependence 50 0.029
539
END035 Endocrine Gland Cancer 49 0.029
540
RTN015 Retinal Cancer 49 0.029
541
ERY017 Erythema Elevatum Diutinum 49 0.029
542
P PCH015 Pachyonychia Congenita 1 49 0.029
543
c PRM226 Primary Central Nervous System Lymphoma 49 0.029
544
GLM004 Gliomatosis Cerebri 49 0.029
545
PRN021 Paranasal Sinus Disease 49 0.029
546
P INT063 Intellectual Disability 49 0.029
547
NCT008 Nicotine Dependence, Protection Against 49 0.029
548
ILT001 Ileitis 49 0.029
549
CCN001 Cocaine Dependence 49 0.029
550
QBC001 Quebec Platelet Disorder 48 0.029
551
MYL003 Myeloid Sarcoma 48 0.029
552
ATN002 Autonomic Nervous System Disease 48 0.029
553
THY030 Thyroid Gland Disease 48 0.029
554
P TRC086 Trichohepatoenteric Syndrome 1 48 0.029
555
P VGN017 Vaginal Cancer 47 0.029
556
PRT030 Parathyroid Gland Disease 47 0.029
557
c CHR418 Chronic Leukemia 47 0.029
558
PLM102 Palmoplantar Keratoderma, Epidermolytic 47 0.029
559
c BPL002 Bipolar I Disorder 47 0.029
560
NLS001 Nelson Syndrome 47 0.029
561
BRD001 Brody Myopathy 47 0.029
562
c CLR017 Clear Cell Sarcoma 46 0.029
563
ART004 Aortic Atherosclerosis 46 0.029
564
P HYP087 Hypotrichosis 46 0.029
565
EMB007 Embryonal Sarcoma 46 0.029
566
P CRN035 Cranial Nerve Palsy 46 0.029
567
P PRM108 Primary Progressive Multiple Sclerosis 46 0.029
568
IDP024 Idiopathic Inflammatory Myopathy 46 0.029
569
P PLN008 Peeling Skin Syndrome 45 0.029
570
URT010 Ureteral Obstruction 45 0.029
571
HDN002 Head Injury 45 0.029
572
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.029
573
C2D001 C2 Deficiency 45 0.029
574
MXD023 Mixed Cell Type Cancer 44 0.029
575
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 44 0.029
576
LYM067 Lymphoid Leukemia 44 0.029
577
LYM012 Lymphoplasmacytic Lymphoma 44 0.029
578
c HMG003 Hemoglobin E Disease 44 0.029
579
BNW001 Bone Ewing's Sarcoma 43 0.029
580
AMN003 Amnestic Disorder 43 0.029
581
ACT058 Active Peptic Ulcer Disease 43 0.029
582
SNS023 Sensory System Cancer 43 0.029
583
MLT001 Multiple Chemical Sensitivity 43 0.029
584
CRB008 Cerebral Atherosclerosis 43 0.029
585
EWN002 Ewing's Family of Tumors 43 0.029
586
P CRB088 Cerebral Atrophy 42 0.029
587
c EST002 Estrogen-Receptor Negative Breast Cancer 42 0.029
588
BHR001 Behr Syndrome 42 0.029
589
PLS016 Plasma Cell Leukemia 42 0.029
590
c BSL024 Basal Cell Carcinoma 1 42 0.029
591
SXL003 Sexual Disorder 42 0.029
592
PRD011 Proud Syndrome 42 0.029
593
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 42 0.029
594
c RCR022 Recurrent Acute Pancreatitis 41 0.029
595
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.029
596
SMT002 Smooth Muscle Tumor 41 0.029
597
VGN020 Vaginal Disease 41 0.029
598
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 41 0.029
599
AYM001 Ayme-Gripp Syndrome 41 0.029
600
CHR413 Chronic Myocardial Ischemia 41 0.029
601
CNV002 Conversion Disorder 41 0.029
602
END038 Endocrine Pancreas Disease 41 0.029
603
c PRK045 Parkinson Disease 5 40 0.029
604
SCH003 Schizophreniform Disorder 40 0.029
605
GST078 Gastrointestinal Allergy 40 0.029
606
BSL008 Basal Ganglia Disease 40 0.029
607
c CHR096 Chronic Pulmonary Heart Disease 40 0.029
608
c PLN018 Peeling Skin Syndrome 2 40 0.029
609
CRN031 Cranial Nerve Disease 40 0.029
610
MST004 Mast Cell Neoplasm 40 0.029
611
ATN003 Autonomic Nervous System Neoplasm 40 0.029
612
PRV003 Perivascular Epithelioid Cell Tumor 39 0.029
613
LYM127 Lymphatic Malformations 39 0.029
614
c HRM017 Hermansky-Pudlak Syndrome 2 39 0.029
615
FST010 Fasting Hypoglycemia 39 0.029
616
ORB013 Orbital Disease 39 0.029
617
LPD001 Lipid Pneumonia 39 0.029
618
HYP030 Hypoactive Sexual Desire Disorder 39 0.029
619
PGM003 Pigmentation Disease 39 0.029
620
ADR009 Adrenal Cortex Disease 39 0.029
621
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.029
622
c ADL001 Adult Lymphoma 39 0.029
623
c INF086 Inflammatory Bowel Disease 3 38 0.029
624
NSL022 Nasal Cavity Disease 38 0.029
625
PHS001 Phosphorus Metabolism Disease 38 0.029
626
c HYP507 Hypotrichosis 1 38 0.029
627
c PRK025 Parkinson Disease 10 38 0.029
628
ADJ001 Adjustment Disorder 38 0.029
629
GST007 Gastric Dilatation 38 0.029
630
c PRK030 Parkinson Disease 4 38 0.029
631
SPC003 Specific Developmental Disorder 38 0.029
632
P UTR038 Uterine Disease 37 0.029
633
BNR001 Bone Remodeling Disease 37 0.029
634
WTH001 Withdrawal Disorder 37 0.029
635
c CNG031 Congenital Nervous System Abnormality 37 0.029
636
MYF001 Myofibroma 37 0.029
637
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.029
638
VSC018 Visceral Steatosis 37 0.029
639
GRM001 Germ Cell and Embryonal Cancer 36 0.029
640
OPT008 Optic Nerve Neoplasm 36 0.029
641
HMF008 Hemifacial Atrophy, Progressive 36 0.029
642
IMM065 Immunodeficiency 10 36 0.029
643
c HRD009 Hereditary Wilms' Tumor 36 0.029
644
LCL004 Localized Osteosarcoma 35 0.029
645
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.029
646
ATM012 Autoimmune Disease of Blood 35 0.029
647
INV004 Invasive Bladder Transitional Cell Carcinoma 35 0.029
648
PRT035 Peritoneum Cancer 35 0.029
649
BNS001 Bone Osteosarcoma 35 0.029
650
IMM078 Immunodeficiency 21 35 0.029
651
c PLM022 Pulmonary Valve Insufficiency 34 0.029
652
c PLN017 Peeling Skin Syndrome 1 34 0.029
653
PRP024 Peripheral Osteosarcoma 34 0.029
654
CHL078 Childhood-Onset Schizophrenia 34 0.029
655
MXD032 Mixed Germ Cell Tumor 34 0.029
656
ANG049 Angioedema Induced by Ace Inhibitors 34 0.029
657
CRD016 Cardiac Rupture 34 0.029
658
CHR079 Choroid Disease 34 0.029
659
FHR001 Fuhrmann Syndrome 34 0.029
660
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.029
661
SWL001 Swallowing Disorders 33 0.029
662
GST020 Gastric Antral Vascular Ectasia 33 0.029
663
HYP114 Hypertensive Nephropathy 33 0.029
664
CRB001 Cerebral Lymphoma 33 0.029
665
CRT045 Creatine Phosphokinase, Elevated Serum 33 0.029
666
LNS003 Lens Disease 33 0.029
667
PDT021 Pediatric Osteosarcoma 33 0.029
668
P ATS049 Autism Susceptibility, X-Linked 2 33 0.029
669
FNC006 Functional Gastric Disease 32 0.029
670
ATY001 Atypical Depressive Disorder 32 0.029
671
CRB040 Cerebrum Cancer 32 0.029
672
P OVR075 Ovarian Dysgenesis 1 32 0.029
673
c LYM106 Lymphoproliferative Syndrome 1 32 0.029
674
P ACT080 Acute Pulmonary Heart Disease 31 0.029
675
CHR463 Chronic Actinic Dermatitis 31 0.029
676
KDN019 Kidney Sarcoma 31 0.029
677
c LNG072 Lung Cancer Susceptibility 2 31 0.029
678
STR018 Steroid Inherited Metabolic Disorder 31 0.029
679
RCT020 Rectum Adenocarcinoma 31 0.029
680
c OVR076 Ovarian Dysgenesis 2 31 0.029
681
IMM102 Immunodeficiency 14 31 0.029
682
IMM082 Immunodeficiency 18 31 0.029
683
IRS003 Iris Disease 31 0.029
684
MXD025 Mixed Germ Cell Cancer 31 0.029
685
JJN007 Jejunal Adenocarcinoma 30 0.029
686
VNW003 Von Willibrand Disease, Type 3 30 0.029
687
c HRD020 Hereditary Renal Cell Carcinoma 30 0.029
688
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 30 0.029
689
c PRK051 Parkinson Disease 18 30 0.029
690
FCL003 Facial Hemiatrophy 30 0.029
691
JJN003 Jejunal Cancer 29 0.029
692
END034 Endocrine Exophthalmos 29 0.029
693
KDN007 Kidney Clear Cell Sarcoma 29 0.029
694
c CLR077 Colorectal Cancer 10 29 0.029
695
c PLN021 Peeling Skin Syndrome 3 29 0.029
696
c TRC078 Trichohepatoenteric Syndrome 2 29 0.029
697
c MNT149 Mental Retardation, X-Linked 3 29 0.029
698
LNG019 Lung Combined Type Small Cell Carcinoma 29 0.029
699
IMM081 Immunodeficiency 19 29 0.029
700
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.029
701
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.029
702
c NRB015 Neuroblastoma 2 28 0.029
703
RDT005 Radiation Induced Cancer 28 0.029
704
c NRB014 Neuroblastoma 3 28 0.029
705
c SCH051 Schizophrenia 4 28 0.029
706
SML003 Small Cell Osteogenic Sarcoma 28 0.029
707
IMM080 Immunodeficiency 23 27 0.029
708
c INF002 Inflammatory Diarrhea 27 0.029
709
c SYS038 Systemic Lupus Erythematosus 2 27 0.029
710
IMM076 Immunodeficiency 24 27 0.029
711
LVR006 Liver Lymphoma 27 0.029
712
c ALZ040 Alzheimer's Disease 11 27 0.029
713
FNC005 Functional Colonic Disease 27 0.029
714
IMM077 Immunodeficiency 20 27 0.029
715
IMM063 Immunodeficiency 15 26 0.029
716
IMM074 Immunodeficiency 16 26 0.029
717
c INF090 Inflammatory Bowel Disease 7 26 0.029
718
IMM075 Immunodeficiency 22 26 0.029
719
KDN002 Kidney Rhabdoid Cancer 26 0.029
720
HMN031 Human Venous Malformation 25 0.029
721
c BSL011 Basal Cell Carcinoma, Multiple 25 0.029
722
P SML002 Small Cell Sarcoma 25 0.029
723
c DFN314 Deafness, Congenital, and Onychodystrophy, Autosomal Dominant 25 0.029
724
c ATM007 Autoimmune Disease of Central Nervous System 25 0.029
725
MXD007 Mixed Hepatoblastoma 24 0.029
726
P ATM050 Autoimmune Thyroid Disease 3 24 0.029
727
RHB011 Rhabdoid Tumor Predisposition Syndrome 2 24 0.029
728
HDG004 Hodgkin's Granuloma 24 0.029
729
c LKM004 Leukemia, B-Cell, Chronic 24 0.029
730
c INF093 Inflammatory Bowel Disease 14 23 0.029
731
CNT067 Central Cord Syndrome 23 0.029
732
UTR031 Uterine Benign Neoplasm 23 0.029
733
PPL023 Pupil Disease 23 0.029
734
c OVR102 Ovarian Dysgenesis 3 22 0.029
735
SCK020 Sickle Cell - Hemoglobin D Disease 22 0.029
736
c OVR107 Ovarian Dysgenesis 4 22 0.029
737
HPD002 Hepadnavirus Infection 22 0.029
738
c RHB021 Rhabdomyosarcoma, Embryonal, 2 21 0.029
739
c PRK022 Parkinson Disease 12 21 0.029
740
HYP213 Hypomelanotic Disorder 21 0.029
741
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.029
742
c RNL016 Renal Infectious Disease 20 0.029
743
c CLR082 Colorectal Cancer 7 20 0.029
744
c WLM005 Wilms Tumor 2 20 0.029
745
P GNR027 Generalized Peeling Skin Syndrome 19 0.029
746
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.029
747
c WLM011 Wilms Tumor 6 19 0.029
748
c VGN016 Vaginal Benign Neoplasm 19 0.029
749
MNT257 Mental Retardation, X-Linked, with Craniofacial Dysmorphism 18 0.029
750
CNT010 Central Nervous System Hematologic Cancer 18 0.029
751
c HYP544 Hypotrichosis 10 18 0.029
752
c ALP039 Alopecia Areata 1 18 0.029
753
c NRB012 Neuroblastoma 5 18 0.029
754
c HYP270 Hypospadias 2, X-Linked 18 0.029
755
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.029
756
KDN010 Kidney Osteogenic Sarcoma 18 0.029
757
c HYP284 Hypospadias 1, X-Linked 17 0.029
758
c PST093 Posterior Hypospadias 17 0.029
759
ACT094 Acute Articular Rheumatism 17 0.029
760
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.029
761
PDT020 Pediatric Germ Cell Cancer 17 0.029
762
HDG006 Hodgkin's Paragranuloma 17 0.029
763
BNP001 Bone Peripheral Neuroepithelioma 17 0.029
764
c BSL025 Basal Cell Carcinoma 2 17 0.029
765
c BSL026 Basal Cell Carcinoma 3 16 0.029
766
c NRB013 Neuroblastoma 6 16 0.029
767
c MNT194 Mental Retardation, X-Linked 50 16 0.029
768
c MNT204 Mental Retardation, X-Linked 23 16 0.029
769
c BLR024 Biliary Cirrhosis, Primary, 1 16 0.029
770
c BLR016 Biliary Cirrhosis, Primary, 2 15 0.029
771
c BLR017 Biliary Cirrhosis, Primary, 3 15 0.029
772
FML006 Female Breast Central Part Cancer 15 0.029
773
MXD009 Mixed Cell Type Kidney Wilms' Tumor 15 0.029
774
MYC003 Myocardium Cancer 14 0.029
775
SFT001 Soft Tissue Peripheral Neuroepithelioma 14 0.029
776
NVD002 Nevada Syndrome 14 0.029
777
c FML303 Familial/multiple Cancer 14 0.029
778
CGL001 Coagulation Protein Disease 14 0.029
779
c CNG343 Congenital Coronary Artery Aneurysm 13 0.029
780
ATM013 Autoimmune Disease of Cardiovascular System 13 0.029
781
P MXD039 Mixed Germ Cell Tumor of Central Nervous System 12 0.029
782
HRP008 Herpes Simiae 12 0.029
783
MXD015 Mixed Type Rhabdomyosarcoma 12 0.029
784
RSS003 Resistance to Lh 12 0.029
785
PDT006 Pediatric Cns Embryonal Cell Carcinoma 11 0.029
786
HRD059 Hereditary Peripheral Nervous Disorder 11 0.029
787
P HYP653 Hypospadias 4, X-Linked 10 0.029
788
VGN002 Vagina Leiomyoma 10 0.029
789
HRP012 Herpesvirus Simiae B Virus 10 0.029
790
MNT033 Mental Retardation X-Linked Dysmorphism 10 0.029
791
MLR004 Malaria 83 0.020
792
HV1006 Hiv-1 80 0.020
793
DCH001 Duchenne Muscular Dystrophy 79 0.020
794
INS024 Insulin-Like Growth Factor I 75 0.020
795
P NRF002 Neurofibromatosis 71 0.020
796
SQM006 Squamous Cell Carcinoma 70 0.020
797
P MTC003 Metachromatic Leukodystrophy 70 0.020
798
PCK002 Pick Disease 68 0.020
799
ANX002 Anxiety Disorder 67 0.020
800
c NRF018 Neurofibromatosis, Type 1 67 0.020
801
CHG001 Chagas Disease 67 0.020
802
P MNN013 Meningitis 67 0.020
803
P NNN008 Noonan Syndrome 1 67 0.020
804
P MYL006 Myeloid Leukemia 66 0.020
805
LSH001 Leishmaniasis 66 0.020
806
INC002 Inclusion Body Myositis 66 0.020
807
BRC012 Brucellosis 66 0.020
808
P MSC005 Muscular Dystrophy 65 0.020
809
P THR014 Thrombocytopenia 64 0.020
810
P PRP003 Porphyria Cutanea Tarda 64 0.020
811
LPP001 Lipoprotein Lipase Deficiency 63 0.020
812
c ATS347 Autosomal Dominant Polycystic Kidney Disease 62 0.020
813
CTN007 Cutaneous Leishmaniasis 62 0.020
814
GLC037 Glucocorticoid Resistance 62 0.020
815
GNG013 Gingivitis 61 0.020
816
P ADL010 Adult Respiratory Distress Syndrome 61 0.020
817
MDD011 Mood Disorder 61 0.020
818
HPY002 H. Pylori Infection 61 0.020
819
P MCP010 Mucopolysaccharidosis 60 0.020
820
ACQ007 Acquired Immunodeficiency Syndrome 60 0.020
821
PLM033 Pulmonary Embolism 60 0.020
822
CLT003 Colitis 60 0.020
823
P CLR108 Colorectal Adenoma 60 0.020
824
GLB001 Gilbert Syndrome 60 0.020
825
P HMN010 Hemangioma 59 0.020
826
GST045 Gastroenteritis 59 0.020
827
P LKD001 Leukodystrophy 59 0.020
828
P PRP029 Porphyria 59 0.020
829
P PLY018 Polycythemia 58 0.020
830
PRP030 Purpura 58 0.020
831
c FML001 Familial Atrial Fibrillation 58 0.020
832
ETN001 Eating Disorder 58 0.020
833
MLG056 Malignant Hyperthermia 58 0.020
834
ALP001 Alopecia Universalis 58 0.020
835
P THR003 Thoracic Aortic Aneurysm 57 0.020
836
P EXN002 Exanthem 57 0.020
837
THR024 Thrombosis 57 0.020
838
GST033 Gestational Diabetes 57 0.020
839
c ACT210 Acute Respiratory Distress Syndrome 57 0.020
840
c SVR001 Severe Acute Respiratory Syndrome 57 0.020
841
c MCR115 Microvascular Complications of Diabetes 5 57 0.020
842
P FBR017 Fibrosarcoma 56 0.020
843
P GST044 Gastritis 56 0.020
844
GST023 Gastric Ulcer 56 0.020
845
THR004 Thrombocytosis 55 0.020
846
P LPD010 Lipodystrophy 55 0.020
847
SPN027 Spinal Stenosis 55 0.020
848
HDC001 Headache 54 0.020
849
c BCT007 Bacterial Meningitis 54 0.020
850
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.020
851
PLM010 Pulmonary Edema 54 0.020
852
P VNS003 Venous Insufficiency 54 0.020
853
P LCH002 Lichen Planus 53 0.020
854
OLV001 Olivopontocerebellar Atrophy 53 0.020
855
c INF023 Inflammatory Breast Carcinoma 52 0.020
856
GST063 Gastric Cancer Risk After H. Pylori Infection 52 0.020
857
PRT011 Protein C Deficiency 52 0.020
858
DGN001 Degenerative Disc Disease 52 0.020
859
MYC002 Mycobacterium Avium Complex Disease 52 0.020
860
P LCT001 Lactic Acidosis 51 0.020
861
P LRS001 Larsen Syndrome 51 0.020
862
c CRB103 Cerebral Cavernous Malformations-1 50 0.020
863
BNF002 Bone Fracture 50 0.020
864
P MSC003 Muscular Atrophy 50 0.020
865
LPD009 Lipid Storage Disease 49 0.020
866
SRT004 Serotonin Syndrome 49 0.020
867
ALD010 Aldosteronism, Glucocorticoid-Remediable 49 0.020
868
SPR099 Supravalvar Aortic Stenosis 49 0.020
869
PRT018 Portal Vein Thrombosis 49 0.020
870
P FML052 Familial Cold Autoinflammatory Syndrome 49 0.020
871
ATN005 Autonomic Dysfunction 49 0.020
872
LMB062 Limb Ischemia 48 0.020
873
LPD004 Lipoid Nephrosis 48 0.020
874
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.020
875
BCT015 Bacteremia 48 0.020
876
PRN023 Prion Disease 48 0.020
877
ADR012 Adrenal Gland Disease 48 0.020
878
RTN003 Retinal Ischemia 48 0.020
879
OCL006 Ocular Hypertension 48 0.020
880
MSS002 Mass Syndrome 48 0.020
881
CRN017 Coronary Thrombosis 48 0.020
882
FSC004 Fasciitis 48 0.020
883
P CMP008 Compartment Syndrome 48 0.020
884
P CTN003 Cutaneous Lupus Erythematosus 48 0.020
885
RTN020 Retinal Vascular Disease 48 0.020
886
P RNV001 Renovascular Hypertension 47 0.020
887
ESN015 Eosinophilic Fasciitis 47 0.020
888
RNL077 Renal Fibrosis 47 0.020
889
P GNT009 Giant Axonal Neuropathy 47 0.020
890
SDD007 Sudden Cardiac Death 47 0.020
891
MGR028 Migraine with or Without Aura 1 47 0.020
892
DBT006 Diabetic Macular Edema 47 0.020
893
CHL056 Cheilitis 46 0.020
894
CVR006 Cavernous Hemangioma 46 0.020
895
NWB001 Newborn Respiratory Distress Syndrome 45 0.020
896
CRB004 Cerebral Artery Occlusion 45 0.020
897
P CRV039 Cervicitis 45 0.020
898
OST003 Osteonecrosis 45 0.020
899
HYP286 Hyperchylomicronemia, Late-Onset 45 0.020
900
P ATR005 Atrophic Gastritis 45 0.020
901
MYC005 Myocardial Stunning 44 0.020
902
P ART084 Arteriovenous Fistula 44 0.020
903
TST015 Testicular Disease 44 0.020
904
CLS010 Cluster Headache 44 0.020
905
DBT008 Diabetic Angiopathy 44 0.020
906
SYS003 Systolic Heart Failure 43 0.020
907
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.020
908
PHY002 Physical Disorder 43 0.020
909
RNL097 Renal Artery Disease 43 0.020
910
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.020
911
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.020
912
HYP088 Hyper-Igd Syndrome 43 0.020
913
P CRD132 Cardiac Conduction Defect 43 0.020
914
PRT019 Protein-Losing Enteropathy 42 0.020
915
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.020
916
FLL031 Follicular Adenoma 42 0.020
917
c HYP011 Hyperlipoproteinemia Type Iii 42 0.020
918
FCT008 Factitious Disorder 41 0.020
919
P RPP002 Rippling Muscle Disease 41 0.020
920
URT001 Urethritis 41 0.020
921
c PRM023 Pre-Malignant Neoplasm 41 0.020
922
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.020
923
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.020
924
c CRB094 Cerebral Cavernous Malformations 3 40 0.020
925
c ALZ042 Alzheimer's Disease 14 40 0.020
926
CRN019 Coronary Artery Vasospasm 40 0.020
927
MNN017 Mononeuropathy 40 0.020
928
PRN037 Prinzmetal's Variant Angina 39 0.020
929
FTT003 Fatty Acid Oxidation Disorders 39 0.020
930
c PCH012 Pachyonychia Congenita 2 38 0.020
931
SCR011 Scrapie 38 0.020
932
MCL006 Macular Retinal Edema 38 0.020
933
HYP034 Hypertensive Encephalopathy 38 0.020
934
OCL010 Ocular Hypotension 38 0.020
935
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.020
936
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.020
937
SXD001 Sex Differentiation Disease 38 0.020
938
CVR010 Cavernous Malformation 37 0.020
939
c CTR098 Cataract 1, Multiple Types 37 0.020
940
ISC005 Ischemic Bone Disease 36 0.020
941
MDD003 Middle Cerebral Artery Infarction 36 0.020
942
CRT013 Carotid Stenosis 36 0.020
943
MCL027 Macular Dystrophy, Dominant Cystoid 36 0.020
944
MCR011 Microinvasive Gastric Cancer 35 0.020
945
c NNN010 Noonan Syndrome 3 35 0.020
946
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.020
947
RDN001 Reading Disorder 34 0.020
948
CNZ001 Coenzyme Q10 Deficiency Disease 34 0.020
949
XNT009 Xanthoma Disseminatum 34 0.020
950
P HYP032 Hyperlipoproteinemia Type Iv 34 0.020
951
c NNN012 Noonan Syndrome 5 33 0.020
952
c CTR132 Cataract 3, Multiple Types 33 0.020
953
DDN007 Duodenal Disease 33 0.020
954
c CTR096 Cataract 6, Multiple Types 33 0.020
955
CHL070 Cholesterol Embolism 32 0.020
956
c ALZ012 Alzheimer Disease 12 32 0.020
957
c CTR125 Cataract 7 32 0.020
958
LCH013 Lichen Planus Pemphigoides 32 0.020
959
CHM006 Chime Syndrome 32 0.020
960
DBT007 Diabetic Cataract 32 0.020
961
c CTR102 Cataract 2, Multiple Types 32 0.020
962
DNT014 Dental Pulp Disease 31 0.020
963
CPM001 Cap Myopathy 30 0.020
964
c GNT027 Giant Axonal Neuropathy-1 30 0.020
965
IMM066 Immunodeficiency 9 30 0.020
966
c FML253 Familial Cold Autoinflammatory Syndrome 3 30 0.020
967
DFC001 Defective Apolipoprotein B-100 29 0.020
968
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.020
969
C9D001 C9 Deficiency 29 0.020
970
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 28 0.020
971
CKS001 Ck Syndrome 27 0.020
972
GST038 Gastrointestinal Adenoma 27 0.020
973
WDS002 Woods Syndrome 27 0.020
974
c ADN040 Adenomas, Multiple Colorectal 27 0.020
975
c CTR127 Cataract 19 27 0.020
976
CNT023 Central Nervous System Hemangioma 26 0.020
977
c NNN025 Noonan Syndrome 10 26 0.020
978
c HYP600 Hyperaldosteronism, Familial, Type Ii 26 0.020
979
c MCR133 Microvascular Complications of Diabetes 4 26 0.020
980
c ALZ039 Alzheimer's Disease 7 26 0.020
981
MRL001 Meralgia Paresthetica 26 0.020
982
CNZ007 Coenzyme Q10 Deficiency, Primary, 2 26 0.020
983
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 26 0.020
984
DNT006 Dental Pulp Necrosis 26 0.020
985
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.020
986
CNZ009 Coenzyme Q10 Deficiency, Primary, 5 24 0.020
987
CRB014 Cerebral Angioma 24 0.020
988
c MJR007 Major Affective Disorder 1 24 0.020
989
EYC003 Eye Accommodation Disease 24 0.020
990
CRN197 Coronary Arterial Fistulas 23 0.020
991
c SYS041 Systemic Lupus Erythematosus 9 23 0.020
992
c CTR106 Cataract 20, Multiple Types 23 0.020
993
c CRB051 Cerebral Cavernous Malformation, Familial 23 0.020
994
CNZ004 Coenzyme Q10 Deficiency, Primary, 3 22 0.020
995
RSP007 Respiratory Distress Syndrome, Infant 22 0.020
996
SNG003 Single Ventricular Heart 22 0.020
997
INS009 Insulin-Resistance Type B 22 0.020
998
PNT003 Pinta Disease 22 0.020
999
CNZ010 Coenzyme Q10 Deficiency, Primary, 7 22 0.020
1000
c CLR081 Colorectal Cancer 6 22 0.020
1001
ATR024 Atrial Fibrillation and Stroke 22 0.020
1002
c CLC048 Celiac Disease 3 21 0.020
1003
CRB087 Cerebral Arteriosclerosis 21 0.020
1004
BNR002 Bone Resorption Disease 21 0.020
1005
MTC025 Mitochondrial Myopathy with Diabetes 21 0.020
1006
SPS090 Sepsis in Premature Infants 21 0.020
1007
c SYS046 Systemic Lupus Erythematosus 3 21 0.020
1008
BRN027 Brain Angioma 21 0.020
1009
c CLC037 Celiac Disease 4 20 0.020
1010
TCR004 Tacrolimus Dose Selection 20 0.020
1011
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.020
1012
CYT018 Cytochrome P450 2d6 Variant 19 0.020
1013
c SCH064 Schizophrenia 10 19 0.020
1014
c MJR008 Major Affective Disorder 2 19 0.020
1015
c ALZ008 Alzheimer Disease Risk Factor 18 0.020
1016
CML001 Cumulative Trauma Disorders 18 0.020
1017
c CTR161 Cataract 19 Multiple Types 18 0.020
1018
c FML110 Familial Cerebral Cavernous Malformation 2 18 0.020
1019
PYL007 Pylorus Cancer 18 0.020
1020
c CLC045 Celiac Disease 2 17 0.020
1021
c SYS047 Systemic Lupus Erythematosus 7 16 0.020
1022
c SYS045 Systemic Lupus Erythematosus 14 16 0.020
1023
GLC077 Glucocorticoid Therapy, Response to 16 0.020
1024
BNM008 Bone Mineral Density, Low 16 0.020
1025
c MJR004 Major Affective Disorder 4 16 0.020
1026
ATR076 Atrophic Muscular Disease 15 0.020
1027
ACT174 Acute Peripheral Arterial Occlusion 15 0.020
1028
c FML109 Familial Cerebral Cavernous Malformation 1 15 0.020
1029
c FML111 Familial Cerebral Cavernous Malformation 3 15 0.020
1030
WSC001 Wisconsin Syndrome 14 0.020
1031
BLN008 Blind Hypotensive Eye 14 0.020
1032
INT074 Intracranial Arteriosclerosis 14 0.020
1033
NVS004 Nova Syndrome 13 0.020
1034
LBR003 Labrador Lung 13 0.020
1035
LRG015 Large Intestine Adenoma 12 0.020
1036
BLN007 Blind Hypertensive Eye 11 0.020
1037
PRM053 Primary Release Disorder of Platelets 11 0.020
1038
c FML158 Familial Hemangioma 11 0.020
1039
CRN073 Coronary Arteries Congenital Malformation 10 0.020
1040
PRM138 Pure Mitochondrial Myopathy 9 0.020
1041
CNG172 Congenital Vascular Cavernous Malformations 8 0.020
1042
CRN080 Craniofacial and Skeletal Defects 5 0.020
Content
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