Search results for Simvastatin

531 hits were found for Simvastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 59 0.483
2
P CRN300 Coronary Heart Disease 1 57 0.323
3
P CRN018 Coronary Artery Anomaly 69 0.320
4
ISC006 Ischemic Heart Disease 73 0.299
5
P HRT032 Heart Disease 80 0.296
6
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.291
7
VSC007 Vascular Disease 71 0.281
8
P DBT009 Diabetes Mellitus 72 0.278
9
ISC004 Ischemia 66 0.277
10
P ART021 Arteriosclerosis 62 0.273
11
ART140 Arteries, Anomalies of 51 0.273
12
GLC008 Glucose Metabolism Disease 38 0.261
13
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.252
14
P MYC007 Myocardial Infarction 81 0.212
15
END072 Endotheliitis 46 0.209
16
P HYP607 Hypercholesterolemia, Familial 81 0.205
17
CRB039 Cerebrovascular Disease 68 0.171
18
P KDN018 Kidney Disease 69 0.169
19
ATM095 Autoimmune Disease 66 0.169
20
GST050 Gastrointestinal System Disease 66 0.164
21
P HYP614 Hyperlipidemia, Familial Combined 57 0.157
22
P LVR013 Liver Disease 76 0.154
23
LNG099 Lung Disease 67 0.143
24
URN009 Urinary System Disease 58 0.143
25
P MLT020 Multiple Sclerosis 85 0.135
26
P INT068 Intestinal Disease 65 0.135
27
HYP060 Hyperinsulinism 56 0.135
28
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.135
29
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.135
30
P PRD008 Periodontitis 67 0.132
31
RSP006 Respiratory System Disease 63 0.132
32
ANR040 Aneurysm 61 0.132
33
P ENC018 Encephalopathy 58 0.129
34
P HPT021 Hepatitis 75 0.126
35
IMM136 Immune System Disease 57 0.126
36
P BRS047 Breast Cancer 100 0.123
37
c CHR089 Chronic Kidney Failure 72 0.123
38
PRP027 Peripheral Vascular Disease 71 0.123
39
P CLR023 Colorectal Cancer 98 0.119
40
LVR012 Liver Cirrhosis 73 0.119
41
c CNT035 Central Nervous System Disease 65 0.119
42
HYP066 Hyperglycemia 64 0.119
43
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.119
44
MNG003 Mungan Syndrome 34 0.119
45
P ALZ034 Alzheimer Disease 95 0.116
46
PSY004 Psychotic Disorder 72 0.116
47
MTH009 Mouth Disease 64 0.116
48
PRP080 Peripheral Artery Disease 54 0.116
49
P NRV007 Nervous System Disease 75 0.113
50
BRS051 Breast Disease 67 0.113
51
CNN005 Connective Tissue Disease 65 0.113
52
RCT017 Rectal Disease 38 0.113
53
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.113
54
MYL069 Myeloma, Multiple 86 0.109
55
P MYP004 Myopathy 69 0.109
56
SKN016 Skin Disease 68 0.109
57
P PLY011 Polycystic Ovary Syndrome 65 0.109
58
AGN016 Aging 65 0.109
59
PRD007 Periodontal Disease 64 0.109
60
P HMR003 Hemorrhagic Disease 61 0.109
61
DMY004 Demyelinating Disease 58 0.109
62
SKN027 Skin Conditions 48 0.109
63
P BLD051 Blood Coagulation Disease 38 0.109
64
VSC008 Vascular Hemostatic Disease 36 0.109
65
P LNG032 Lung Cancer 99 0.105
66
P RHM011 Rheumatoid Arthritis 91 0.105
67
AST005 Asthma 83 0.105
68
P ART022 Arthritis 77 0.105
69
CNG034 Congestive Heart Failure 74 0.105
70
P PRT013 Portal Hypertension 59 0.105
71
CLN019 Colonic Disease 55 0.105
72
ANG054 Angina Pectoris 53 0.105
73
c BLD140 Blood Group, I System 37 0.105
74
DMN002 Dementia 68 0.101
75
END030 End Stage Renal Failure 59 0.101
76
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.097
77
P SCH015 Schizophrenia 71 0.097
78
SMT004 Smith-Lemli-Opitz Syndrome 70 0.097
79
PRT036 Peritonitis 67 0.097
80
P OVR049 Ovarian Disease 58 0.097
81
P OVR046 Ovarian Cyst 52 0.097
82
PLS009 Plasma Cell Neoplasm 51 0.097
83
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.097
84
c MTR002 Mitral Valve Insufficiency 46 0.097
85
GND003 Gonadal Disease 32 0.097
86
c PLY105 Polycystic Ovary Syndrome 1 30 0.097
87
c HYP595 Hypertension, Essential 78 0.093
88
P LPS004 Lupus Erythematosus 69 0.093
89
ACQ007 Acquired Immunodeficiency Syndrome 65 0.093
90
c HPT003 Hepatitis a 63 0.093
91
P INF032 Infertility 59 0.093
92
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.093
93
GLC003 Glucose Intolerance 58 0.093
94
SPS003 Spastic Diplegia 55 0.093
95
GNG011 Gingival Disease 50 0.093
96
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.093
97
P BRN120 Bronchus Cancer 39 0.093
98
c SYS001 Systemic Lupus Erythematosus 86 0.089
99
STR067 Stroke, Ischemic 84 0.089
100
P PLM037 Pulmonary Hypertension 79 0.089
101
c ACT075 Acute Myocardial Infarction 64 0.089
102
P PNC044 Pancreatitis 64 0.089
103
PNC034 Pancreas Disease 59 0.089
104
CRT016 Carotid Artery Disease 58 0.089
105
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.089
106
P HYP750 Hypertriglyceridemia, Familial 55 0.089
107
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.089
108
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.089
109
ANX010 Anxiety 72 0.084
110
P ADN016 Adenocarcinoma 71 0.084
111
P MYS005 Myositis 63 0.084
112
RHM027 Rheumatic Disease 62 0.084
113
MSC033 Muscle Disorders 53 0.084
114
SCH012 Schizoaffective Disorder 51 0.084
115
c PRD040 Periodontitis, Chronic 49 0.084
116
MSC004 Muscle Tissue Disease 39 0.084
117
ENT004 Enthesopathy 38 0.084
118
RFR001 Refractory Plasma Cell Neoplasm 19 0.084
119
P PRS040 Prostate Cancer 88 0.080
120
P PNM007 Pneumonia 70 0.080
121
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.080
122
VRL011 Viral Infectious Disease 64 0.080
123
P NRP001 Neuropathy 63 0.080
124
NRT004 Neuritis 55 0.080
125
P AMY004 Amyloidosis 69 0.074
126
P ART023 Arthropathy 68 0.074
127
P CLC063 Celiac Disease 1 65 0.074
128
MNT002 Mental Depression 60 0.074
129
JNT002 Joint Disorders 60 0.074
130
BRN038 Bronchial Disease 58 0.074
131
P ALP008 Alopecia 56 0.074
132
c ACT071 Acute Kidney Failure 54 0.074
133
P CLL015 Collagen Disease 53 0.074
134
STM006 Stomach Disease 52 0.074
135
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.074
136
PRD004 Prediabetes Syndrome 46 0.074
137
LYM024 Lymphatic System Disease 45 0.074
138
P PNC035 Pancreatic Cancer 89 0.069
139
CYS001 Cystic Fibrosis 85 0.069
140
GST053 Gastric Cancer 84 0.069
141
P LKM002 Leukemia 75 0.069
142
c SML038 Small Cell Cancer of the Lung 67 0.069
143
VRC005 Varicose Veins 64 0.069
144
P ALP009 Alopecia Areata 64 0.069
145
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.069
146
FTT001 Fatty Liver Disease 62 0.069
147
NRM005 Neuromuscular Disease 60 0.069
148
P DRR001 Diarrhea 60 0.069
149
ESP023 Esophageal Disease 58 0.069
150
PRS042 Prostate Disease 56 0.069
151
MYM001 Myoma 56 0.069
152
BRN071 Brain Injury 54 0.069
153
TRM010 Traumatic Brain Injury 54 0.069
154
OPT009 Optic Neuritis 53 0.069
155
ESP002 Esophageal Varix 46 0.069
156
HRT012 Heart Valve Disease 45 0.069
157
SCH003 Schizophreniform Disorder 44 0.069
158
CRB009 Cerebritis 41 0.069
159
MVM001 Movement Disease 40 0.069
160
P CNN004 Connective Tissue Cancer 35 0.069
161
SCK003 Sickle Cell Anemia 73 0.063
162
CRZ001 Crouzon Syndrome 71 0.063
163
P MJR001 Major Depressive Disorder 70 0.063
164
P EPL164 Epilepsy 70 0.063
165
P ATR011 Atrial Fibrillation 68 0.063
166
LYM007 Lymphangioleiomyomatosis 68 0.063
167
c ART101 Aortic Valve Disease 2 65 0.063
168
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.063
169
P UVT001 Uveitis 61 0.063
170
INT002 Intermittent Claudication 61 0.063
171
CLF027 Cleft Palate, Isolated 61 0.063
172
P NPH012 Nephrotic Syndrome 60 0.063
173
P HYP040 Hypospadias 60 0.063
174
TRN015 Transient Cerebral Ischemia 58 0.063
175
LMY002 Leiomyoma 58 0.063
176
P SML001 Small Cell Carcinoma 58 0.063
177
DCT002 Ductal Carcinoma in Situ 56 0.063
178
c INS002 in Situ Carcinoma 56 0.063
179
c BRS049 Breast Carcinoma in Situ 55 0.063
180
BRS099 Breast Ductal Carcinoma 55 0.063
181
P SZR006 Seizure Disorder 55 0.063
182
SCK005 Sickle Cell Disease 54 0.063
183
PRP019 Peripheral Nervous System Disease 53 0.063
184
HMG005 Hemoglobinopathy 53 0.063
185
LPD009 Lipid Storage Disease 53 0.063
186
HYP043 Hyperandrogenism 50 0.063
187
c HYP740 Hyperlipoproteinemia, Type V 48 0.063
188
DYS018 Dysostosis 48 0.063
189
HYP748 Hypertelorism 46 0.063
190
BRN080 Brain Ischemia 45 0.063
191
GNT050 Genitourinary Tract Anomalies 41 0.063
192
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.063
193
P CRB088 Cerebral Atrophy 38 0.063
194
P VSC018 Visceral Steatosis 38 0.063
195
c OPT050 Opitz Gbbb Syndrome, Type Ii 38 0.063
196
DLT018 Dilution, Pigmentary 37 0.063
197
PNL013 Penile Disease 37 0.063
198
PGM003 Pigmentation Disease 36 0.063
199
HYP213 Hypomelanotic Disorder 25 0.063
200
UVL003 Uveal Diseases 23 0.063
201
P PRK057 Parkinson Disease, Late-Onset 78 0.056
202
P OST002 Osteoporosis 75 0.056
203
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.056
204
P END044 Endometriosis 71 0.056
205
P LYM118 Lymphoma 71 0.056
206
P TBR001 Tuberous Sclerosis 69 0.056
207
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.056
208
MDD011 Mood Disorder 64 0.056
209
c TBR025 Tuberous Sclerosis 1 63 0.056
210
HYP056 Hypoglycemia 62 0.056
211
THR024 Thrombosis 61 0.056
212
LMY014 Leiomyoma, Uterine 61 0.056
213
P RHB003 Rhabdomyosarcoma 61 0.056
214
P BPL003 Bipolar Disorder 61 0.056
215
ALL006 Allergic Asthma 60 0.056
216
DBT010 Diabetic Neuropathy 60 0.056
217
c PCH015 Pachyonychia Congenita 1 59 0.056
218
SLP005 Sleep Disorder 59 0.056
219
P PLM034 Pulmonary Emphysema 59 0.056
220
RTN018 Retinal Disease 56 0.056
221
NNL002 Nonalcoholic Steatohepatitis 56 0.056
222
c MYT020 Myotonic Dystrophy 2 56 0.056
223
INT007 Intermediate Coronary Syndrome 55 0.056
224
ERY017 Erythema Elevatum Diutinum 54 0.056
225
P DBT005 Diabetes Insipidus 54 0.056
226
IMP005 Impotence 54 0.056
227
P CHR345 Chronic Pain 52 0.056
228
P LCT001 Lactic Acidosis 51 0.056
229
IDP024 Idiopathic Inflammatory Myopathy 49 0.056
230
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.056
231
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.056
232
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.056
233
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.056
234
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.056
235
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.056
236
c HRM017 Hermansky-Pudlak Syndrome 2 45 0.056
237
BSL008 Basal Ganglia Disease 44 0.056
238
NRN002 Neuronitis 43 0.056
239
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.056
240
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.056
241
MYF001 Myofibroma 42 0.056
242
INT053 Intracranial Vasospasm 25 0.056
243
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.056
244
MNS002 Mini Stroke 23 0.056
245
P AST055 Asthma-Related Traits 1 18 0.056
246
P HPT023 Hepatocellular Carcinoma 94 0.049
247
LYM133 Lymphoma, Hodgkin, Classic 78 0.049
248
P BLD134 Bladder Cancer 78 0.049
249
P RTN024 Retinoblastoma 76 0.049
250
c LKM071 Leukemia, Chronic Lymphocytic 75 0.049
251
P NRB001 Neuroblastoma 73 0.049
252
EWN003 Ewing Sarcoma 72 0.049
253
ADR007 Adrenoleukodystrophy 72 0.049
254
BRN028 Brain Cancer 72 0.049
255
P RSP003 Respiratory Failure 71 0.049
256
WRN001 Werner Syndrome 70 0.049
257
OST159 Osteogenic Sarcoma 70 0.049
258
c WLM013 Wilms Tumor 1 69 0.049
259
c HPT016 Hepatitis B 68 0.049
260
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.049
261
SRC014 Sarcoma 68 0.049
262
P MCL013 Mucolipidosis Iv 67 0.049
263
BRN024 Bronchitis 67 0.049
264
SPN186 Spinal Cord Injury 67 0.049
265
P KDN017 Kidney Cancer 66 0.049
266
P MCR115 Microvascular Complications of Diabetes 5 66 0.049
267
P LYM026 Lymphoblastic Leukemia 66 0.049
268
GST045 Gastroenteritis 65 0.049
269
P DRM010 Dermatomyositis 65 0.049
270
P WLD002 Waldenstrom Macroglobulinemia 65 0.049
271
ALC007 Alcohol Dependence 65 0.049
272
CRB011 Cerebrotendinous Xanthomatosis 64 0.049
273
ADN018 Adenoma 63 0.049
274
CRD119 Cardiac Arrest 63 0.049
275
P SNS014 Sinusitis 62 0.049
276
P HYP086 Hypothyroidism 62 0.049
277
P GRV001 Graves' Disease 62 0.049
278
c ACT027 Acute Pancreatitis 61 0.049
279
HYP266 Hypoxia 61 0.049
280
NRV006 Nervous System Cancer 61 0.049
281
MCS002 Mucositis 61 0.049
282
OCL009 Ocular Cancer 61 0.049
283
P GLM045 Glioma 61 0.049
284
P CTR002 Cataract 60 0.049
285
P PLY014 Polycystic Kidney Disease 60 0.049
286
P GST049 Gastrointestinal System Cancer 60 0.049
287
RHM001 Rheumatic Fever 59 0.049
288
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.049
289
BNC003 Bone Cancer 59 0.049
290
P INT030 Intracranial Aneurysm 58 0.049
291
P PLY019 Polyneuropathy 58 0.049
292
SFT003 Soft Tissue Sarcoma 58 0.049
293
LYM019 Lymphosarcoma 58 0.049
294
TRN018 Transitional Cell Carcinoma 58 0.049
295
HMR039 Hemorrhage, Intracerebral 57 0.049
296
IMM158 Immune Suppression 57 0.049
297
ATY005 Atypical Teratoid Rhabdoid Tumor 57 0.049
298
ECT006 Ectodermal Dysplasia 57 0.049
299
CHR081 Choroideremia 57 0.049
300
P MYP006 Myopia 56 0.049
301
P HYP076 Hyperthyroidism 56 0.049
302
BLD044 Bladder Disease 55 0.049
303
HPT022 Hepatoblastoma 55 0.049
304
HDC001 Headache 55 0.049
305
P TRC086 Trichohepatoenteric Syndrome 1 54 0.049
306
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.049
307
RHM028 Rheumatic Heart Disease 54 0.049
308
MCR004 Macroglobulinemia 54 0.049
309
SPN041 Spinal Cord Disease 54 0.049
310
GTR002 Goiter 53 0.049
311
RCT018 Rectal Neoplasm 53 0.049
312
XNT003 Xanthomatosis 53 0.049
313
KRT009 Keratosis 53 0.049
314
MSC072 Muscle Cancer 53 0.049
315
OPT006 Optic Nerve Disease 53 0.049
316
RTN015 Retinal Cancer 53 0.049
317
P EST001 Estrogen-Receptor Positive Breast Cancer 52 0.049
318
DBT004 Diabetic Polyneuropathy 51 0.049
319
PRN021 Paranasal Sinus Disease 51 0.049
320
CLC006 Calcinosis 51 0.049
321
NTR046 Neutrophil Migration 51 0.049
322
THY030 Thyroid Gland Disease 51 0.049
323
c MLG074 Malignant Mesenchymoma 51 0.049
324
NSD001 Nose Disease 51 0.049
325
RHB001 Rhabdoid Cancer 51 0.049
326
EXP004 Exophthalmos 50 0.049
327
LYM012 Lymphoplasmacytic Lymphoma 50 0.049
328
c CLR017 Clear Cell Sarcoma 50 0.049
329
c BPL002 Bipolar I Disorder 50 0.049
330
c WLM018 Wilms Tumor 5 49 0.049
331
MTB004 Metabolic Acidosis 49 0.049
332
EWN002 Ewing's Family of Tumors 49 0.049
333
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.049
334
HDN002 Head Injury 48 0.049
335
CRB085 Cerebral Hemorrhage 47 0.049
336
P NLD001 Nail Disease 47 0.049
337
CRN031 Cranial Nerve Disease 45 0.049
338
SXL003 Sexual Disorder 45 0.049
339
HMF008 Hemifacial Atrophy, Progressive 44 0.049
340
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 44 0.049
341
LYM067 Lymphoid Leukemia 43 0.049
342
PRV003 Perivascular Epithelioid Cell Tumor 42 0.049
343
ORB013 Orbital Disease 40 0.049
344
BNS001 Bone Osteosarcoma 38 0.049
345
c PLM022 Pulmonary Valve Insufficiency 38 0.049
346
CHR079 Choroid Disease 37 0.049
347
CMP028 Complement Component 2 Deficiency 37 0.049
348
c LKM004 Leukemia, B-Cell, Chronic 37 0.049
349
GST020 Gastric Antral Vascular Ectasia 37 0.049
350
P GRM010 Germ Cells Tumors 37 0.049
351
GNR003 Generalized Atherosclerosis 35 0.049
352
RHM035 Rheumatic Fever-Related Antigen 34 0.049
353
END034 Endocrine Exophthalmos 34 0.049
354
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.049
355
FCL003 Facial Hemiatrophy 31 0.049
356
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 31 0.049
357
HDG004 Hodgkin's Granuloma 28 0.049
358
RCT020 Rectum Adenocarcinoma 25 0.049
359
c RHB011 Rhabdoid Tumor Predisposition Syndrome 2 25 0.049
360
c MYC058 Myocardial Infarction 2 25 0.049
361
ACT094 Acute Articular Rheumatism 21 0.049
362
HDG006 Hodgkin's Paragranuloma 21 0.049
363
HRP008 Herpes Simiae 16 0.049
364
HPD002 Hepadnavirus Infection 14 0.049
365
INS024 Insulin-Like Growth Factor I 83 0.040
366
P NNN008 Noonan Syndrome 1 77 0.040
367
c HPT073 Hepatitis C Virus 73 0.040
368
c HPT001 Hepatitis C 73 0.040
369
MLN008 Melanoma 72 0.040
370
BRC012 Brucellosis 71 0.040
371
ART016 Aortic Aneurysm 70 0.040
372
P ADL010 Adult Respiratory Distress Syndrome 67 0.040
373
DRM006 Dermatitis 67 0.040
374
c ACT210 Acute Respiratory Distress Syndrome 63 0.040
375
PLM033 Pulmonary Embolism 62 0.040
376
P EXN002 Exanthem 62 0.040
377
c MCR129 Microvascular Complications of Diabetes 1 62 0.040
378
P GLM007 Glomerulonephritis 61 0.040
379
P HMN010 Hemangioma 61 0.040
380
c THR092 Thrombophilia Due to Thrombin Defect 61 0.040
381
c SCL052 Scleroderma, Familial Progressive 60 0.040
382
PRS047 Prostatitis 59 0.040
383
P LPD010 Lipodystrophy 57 0.040
384
P CRB048 Cerebral Cavernous Malformations 57 0.040
385
NWB001 Newborn Respiratory Distress Syndrome 56 0.040
386
c FML116 Familial Cold Autoinflammatory Syndrome 1 56 0.040
387
P THY032 Thyroiditis 56 0.040
388
P FML052 Familial Cold Autoinflammatory Syndrome 55 0.040
389
P CRD132 Cardiac Conduction Defect 53 0.040
390
P HRD018 Hair Disease 53 0.040
391
ILT001 Ileitis 52 0.040
392
RTN023 Retinitis 52 0.040
393
MCL006 Macular Retinal Edema 51 0.040
394
PRT018 Portal Vein Thrombosis 50 0.040
395
P GNT009 Giant Axonal Neuropathy 50 0.040
396
PRM020 Premenstrual Tension 49 0.040
397
URT010 Ureteral Obstruction 49 0.040
398
DBT008 Diabetic Angiopathy 48 0.040
399
P HYP087 Hypotrichosis 48 0.040
400
CVR006 Cavernous Hemangioma 48 0.040
401
c PCH012 Pachyonychia Congenita 2 47 0.040
402
ATN004 Autonomic Neuropathy 46 0.040
403
EPD070 Epidermoid Cysts 46 0.040
404
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.040
405
ACT058 Active Peptic Ulcer Disease 43 0.040
406
CVR010 Cavernous Malformation 40 0.040
407
CRN020 Coronary Restenosis 38 0.040
408
c GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 36 0.040
409
CHR463 Chronic Actinic Dermatitis 34 0.040
410
c TRC078 Trichohepatoenteric Syndrome 2 34 0.040
411
c HYP600 Hyperaldosteronism, Familial, Type Ii 33 0.040
412
RSP007 Respiratory Distress Syndrome, Infant 28 0.040
413
c CRB051 Cerebral Cavernous Malformation, Familial 20 0.040
414
MLR004 Malaria 86 0.028
415
P OVR042 Ovarian Cancer 82 0.028
416
c MCL042 Macular Degeneration, Age-Related, 1 79 0.028
417
PLY001 Polycythemia Vera 75 0.028
418
SQM006 Squamous Cell Carcinoma 74 0.028
419
MSC157 Muscular Dystrophy, Duchenne Type 74 0.028
420
P MTC003 Metachromatic Leukodystrophy 72 0.028
421
CHG001 Chagas Disease 72 0.028
422
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.028
423
LSH001 Leishmaniasis 71 0.028
424
P MNN013 Meningitis 71 0.028
425
P MYL006 Myeloid Leukemia 69 0.028
426
P PLM036 Pulmonary Fibrosis 68 0.028
427
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.028
428
P PRP003 Porphyria Cutanea Tarda 67 0.028
429
P MSC005 Muscular Dystrophy 66 0.028
430
CTN007 Cutaneous Leishmaniasis 66 0.028
431
P HYP061 Hypertrophic Cardiomyopathy 65 0.028
432
P THR014 Thrombocytopenia 65 0.028
433
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.028
434
INC002 Inclusion Body Myositis 64 0.028
435
GNG013 Gingivitis 64 0.028
436
HLC007 Helicobacter Pylori Infection 64 0.028
437
WLL001 Williams-Beuren Syndrome 63 0.028
438
PNC033 Pancreas Adenocarcinoma 63 0.028
439
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.028
440
OST003 Osteonecrosis 63 0.028
441
CLT003 Colitis 63 0.028
442
GST033 Gestational Diabetes 62 0.028
443
P PRP029 Porphyria 62 0.028
444
PRP030 Purpura 61 0.028
445
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.028
446
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.028
447
P FBR017 Fibrosarcoma 61 0.028
448
P GST044 Gastritis 61 0.028
449
LYS012 Lysosomal Acid Lipase Deficiency 60 0.028
450
SPN027 Spinal Stenosis 60 0.028
451
P PLY018 Polycythemia 60 0.028
452
P HYP724 Hyperlipoproteinemia, Type Iii 59 0.028
453
c BCT007 Bacterial Meningitis 59 0.028
454
CMP010 Complex Regional Pain Syndrome 58 0.028
455
P LCH002 Lichen Planus 58 0.028
456
VSC002 Vascular Dementia 58 0.028
457
LKD001 Leukodystrophy 57 0.028
458
BRN004 Brain Edema 57 0.028
459
GST023 Gastric Ulcer 57 0.028
460
BNF002 Bone Fracture 56 0.028
461
c HYP731 Hyperaldosteronism, Familial, Type I 56 0.028
462
P MSC003 Muscular Atrophy 55 0.028
463
P MMB011 Membranous Nephropathy 55 0.028
464
THR004 Thrombocytosis 55 0.028
465
DGN001 Degenerative Disc Disease 55 0.028
466
c MCR113 Microvascular Complications of Diabetes 3 55 0.028
467
P PRM006 Primary Biliary Cirrhosis 55 0.028
468
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.028
469
P HYP014 Hyperuricemia 54 0.028
470
SPR004 Supravalvular Aortic Stenosis 54 0.028
471
TTH006 Tooth Disease 54 0.028
472
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.028
473
P CTN003 Cutaneous Lupus Erythematosus 53 0.028
474
P OBS001 Obstructive Jaundice 53 0.028
475
c PNS012 Paine Syndrome 52 0.028
476
ESN015 Eosinophilic Fasciitis 52 0.028
477
CRN030 Coronary Stenosis 52 0.028
478
CRT013 Carotid Stenosis 52 0.028
479
LMB062 Limb Ischemia 52 0.028
480
P ATR005 Atrophic Gastritis 51 0.028
481
PRN023 Prion Disease 51 0.028
482
RTN003 Retinal Ischemia 50 0.028
483
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 50 0.028
484
P CRV039 Cervicitis 49 0.028
485
HYP088 Hyper-Igd Syndrome 49 0.028
486
RNL077 Renal Fibrosis 49 0.028
487
FSC004 Fasciitis 48 0.028
488
P RNV001 Renovascular Hypertension 48 0.028
489
P FML035 Familial Hyperlipidemia 48 0.028
490
P CMP008 Compartment Syndrome 48 0.028
491
CHL056 Cheilitis 47 0.028
492
MYC005 Myocardial Stunning 47 0.028
493
P ART084 Arteriovenous Fistula 46 0.028
494
MCR011 Microinvasive Gastric Cancer 45 0.028
495
PRN037 Prinzmetal's Variant Angina 44 0.028
496
URT001 Urethritis 44 0.028
497
ASP030 Aspirin Resistance 44 0.028
498
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.028
499
ACT167 Acute Generalized Exanthematous Pustulosis 42 0.028
500
MNN017 Mononeuropathy 42 0.028
501
CRB086 Cerebral Aneurysms 42 0.028
502
CRN019 Coronary Artery Vasospasm 42 0.028
503
c MCR130 Microvascular Complications of Diabetes 6 42 0.028
504
P RPP006 Rippling Muscle Disease 2 42 0.028
505
FLL031 Follicular Adenoma 41 0.028
506
ALP097 Alopecia Universalis Congenita 40 0.028
507
PRT019 Protein-Losing Enteropathy 40 0.028
508
SCR011 Scrapie 40 0.028
509
c GLL024 Gallbladder Disease 1 39 0.028
510
DNT014 Dental Pulp Disease 39 0.028
511
P TRC005 Tracheal Stenosis 39 0.028
512
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.028
513
XNT009 Xanthoma Disseminatum 38 0.028
514
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.028
515
LCH013 Lichen Planus Pemphigoides 36 0.028
516
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.028
517
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.028
518
SML011 Smoldering Myeloma 34 0.028
519
c MCR120 Microvascular Complications of Diabetes 7 34 0.028
520
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.028
521
ALP072 Alpha-Fetoprotein Deficiency 32 0.028
522
c MCR133 Microvascular Complications of Diabetes 4 32 0.028
523
c CTR119 Cataract 32, Multiple Types 32 0.028
524
DFC001 Defective Apolipoprotein B-100 31 0.028
525
CHL070 Cholesterol Embolism 31 0.028
526
P KLZ004 Kala-Azar 1 31 0.028
527
ATM052 Autoimmune Disease 1 30 0.028
528
DNT006 Dental Pulp Necrosis 29 0.028
529
P RNG031 Ring Chromosome Y Syndrome 29 0.028
530
P MRL001 Meralgia Paresthetica 28 0.028
531
P STR035 Streptococcal Group a Invasive Disease 28 0.028
Content
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