Search results for Pravastatin

618 hits were found for Pravastatin

# Family MCID Name MIFTS Score
1
c HYP836 Hypercholesterolemia, Familial, 1 73 32.921
2
P CRN300 Coronary Heart Disease 1 73 17.287
3
LPD008 Lipid Metabolism Disorder 62 16.621
4
LPP008 Lipoprotein Quantitative Trait Locus 65 14.501
5
ATH013 Atherosclerosis Susceptibility 63 13.501
6
c PRC016 Pre-Eclampsia 65 13.367
7
ART140 Arteries, Anomalies of 53 12.463
8
c FML021 Familial Hypercholesterolemia 72 12.166
9
P MYP004 Myopathy 67 11.350
10
INT007 Intermediate Coronary Syndrome 54 10.724
11
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 10.601
12
P HRT032 Heart Disease 81 10.331
13
P VSC007 Vascular Disease 63 9.516
14
FML035 Familial Hyperlipidemia 55 9.468
15
ISC004 Ischemia 61 8.673
16
P MYC007 Myocardial Infarction 70 8.105
17
P HYP750 Hypertriglyceridemia, Familial 62 7.980
18
PRT251 Proteinuria, Chronic Benign 57 7.648
19
P DBT009 Diabetes Mellitus 67 7.329
20
ANG054 Angina Pectoris 66 7.308
21
P ECL001 Eclampsia 52 7.094
22
P KDN018 Kidney Disease 72 7.093
23
c TYP009 Type 2 Diabetes Mellitus 92 7.068
24
c CHR684 Chronic Kidney Disease 69 6.917
25
P ART021 Arteriosclerosis 54 6.760
26
c ACT075 Acute Myocardial Infarction 56 6.558
27
P CRD246 Cardiovascular System Disease 56 6.200
28
P MYS005 Myositis 56 5.621
29
P HYP838 Hyperlipidemia, Familial Combined, 3 61 5.423
30
c HYP595 Hypertension, Essential 85 5.411
31
PRP027 Peripheral Vascular Disease 71 5.367
32
P NPH012 Nephrotic Syndrome 60 5.312
33
STR067 Stroke, Ischemic 80 5.223
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 5.184
35
c ACT071 Acute Kidney Failure 60 5.099
36
P HPT023 Hepatocellular Carcinoma 96 5.072
37
c MCR130 Microvascular Complications of Diabetes 6 41 5.064
38
c MCR120 Microvascular Complications of Diabetes 7 47 5.064
39
c MCR113 Microvascular Complications of Diabetes 3 52 5.064
40
c MCR133 Microvascular Complications of Diabetes 4 41 5.064
41
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 4.976
42
GLC003 Glucose Intolerance 54 4.915
43
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 4.848
44
c HNT011 Huntington Disease-Like 3 34 4.835
45
c HYP724 Hyperlipoproteinemia, Type Iii 67 4.690
46
CNG034 Congestive Heart Failure 69 4.583
47
END086 End Stage Renal Disease 52 4.582
48
P PLY014 Polycystic Kidney Disease 69 4.576
49
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 4.576
50
HTC003 Hutchinson-Gilford Progeria Syndrome 65 4.545
51
c HNT004 Huntington Disease-Like 2 52 4.531
52
c GLL024 Gallbladder Disease 1 52 4.463
53
HMN014 Human Immunodeficiency Virus Infectious Disease 54 4.445
54
c HYP272 Hypercholesterolemia, Familial, 3 45 4.366
55
c LKM061 Leukemia, Acute Myeloid 83 4.288
56
HYP066 Hyperglycemia 61 4.222
57
CRB039 Cerebrovascular Disease 66 4.205
58
PLC008 Placenta Disease 49 4.189
59
TRN015 Transient Cerebral Ischemia 63 4.126
60
LVR012 Liver Cirrhosis 63 4.089
61
P ART022 Arthritis 71 4.078
62
48X005 48,xyyy 39 3.937
63
HYP060 Hyperinsulinism 54 3.895
64
P LPS004 Lupus Erythematosus 61 3.889
65
P ANT006 Antiphospholipid Syndrome 55 3.876
66
PRT036 Peritonitis 65 3.768
67
P LKM002 Leukemia 67 3.604
68
CRB004 Cerebral Artery Occlusion 45 3.580
69
c SYS001 Systemic Lupus Erythematosus 87 3.575
70
CRD132 Cardiac Conduction Defect 60 3.556
71
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 3.497
72
P PNM007 Pneumonia 67 3.490
73
CHL068 Cholestasis 61 3.490
74
ANR040 Aneurysm 61 3.480
75
P SCH015 Schizophrenia 74 3.471
76
ART004 Aortic Atherosclerosis 47 3.463
77
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.410
78
CYT002 Cytokine Deficiency 43 3.398
79
P PLM036 Pulmonary Fibrosis 66 3.351
80
PRD004 Prediabetes Syndrome 52 3.311
81
P LVR013 Liver Disease 69 3.288
82
P PLM037 Pulmonary Hypertension 72 3.275
83
P EXN002 Exanthem 58 3.254
84
P ALZ034 Alzheimer Disease 87 3.248
85
c HPT001 Hepatitis C 62 3.247
86
P ESP024 Esophagitis 60 3.214
87
c SVR005 Severe Pre-Eclampsia 50 3.181
88
P LNG032 Lung Cancer 98 3.180
89
P ATR011 Atrial Fibrillation 66 3.138
90
c SML038 Small Cell Cancer of the Lung 69 3.083
91
P MYL006 Myeloid Leukemia 61 3.081
92
c HYP740 Hyperlipoproteinemia, Type V 53 3.064
93
c HPT073 Hepatitis C Virus 71 3.060
94
KWS002 Kawasaki Disease 65 2.982
95
SCH012 Schizoaffective Disorder 50 2.964
96
IMM167 Immune Deficiency Disease 78 2.912
97
P HYP086 Hypothyroidism 69 2.874
98
P GST053 Gastric Cancer 83 2.866
99
P AST005 Asthma 76 2.825
100
PRP080 Peripheral Artery Disease 54 2.792
101
ESP021 Esophageal Cancer 83 2.759
102
HMZ003 Homozygous Familial Hypercholesterolemia 60 2.737
103
CLT003 Colitis 63 2.726
104
ANT039 Antisynthetase Syndrome 55 2.648
105
P PNC044 Pancreatitis 61 2.622
106
BNR002 Bone Resorption Disease 47 2.616
107
c MCR115 Microvascular Complications of Diabetes 5 65 2.609
108
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.560
109
OST003 Osteonecrosis 61 2.560
110
P CRN074 Coronary Artery Aneurysm 42 2.560
111
FTT001 Fatty Liver Disease 62 2.502
112
c VRL010 Viral Hepatitis 53 2.502
113
P BRS047 Breast Cancer 98 2.494
114
MYL009 Myelodysplastic Syndrome 67 2.492
115
NNL006 Non-Alcoholic Steatohepatitis 54 2.482
116
GLM044 Glomerular Disease 35 2.442
117
XNT003 Xanthomatosis 49 2.442
118
CRB011 Cerebrotendinous Xanthomatosis 65 2.442
119
P RSP003 Respiratory Failure 74 2.442
120
P OST002 Osteoporosis 76 2.441
121
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.441
122
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.441
123
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.440
124
P NTR004 Neutropenia 63 2.415
125
P FCL005 Focal Segmental Glomerulosclerosis 57 2.415
126
P MYC084 Mycobacterium Tuberculosis 1 68 2.412
127
ART016 Aortic Aneurysm 68 2.400
128
c ATR087 Atrial Standstill 1 74 2.389
129
CRT013 Carotid Stenosis 51 2.380
130
P ANR048 Aniridia 1 64 2.369
131
GT001 Gout 64 2.344
132
P GLM007 Glomerulonephritis 60 2.344
133
HYP266 Hypoxia 57 2.344
134
CRT016 Carotid Artery Disease 52 2.336
135
P EST001 Estrogen-Receptor Positive Breast Cancer 49 2.286
136
P RHM011 Rheumatoid Arthritis 82 2.279
137
PLM010 Pulmonary Edema 55 2.249
138
P TXP001 Toxoplasmosis 60 2.249
139
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.226
140
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.226
141
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.226
142
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.226
143
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.226
144
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.226
145
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.226
146
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.226
147
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.226
148
P NRB001 Neuroblastoma 66 2.226
149
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.226
150
MYC005 Myocardial Stunning 46 2.226
151
CHL079 Children's Interstitial Lung Disease 26 2.226
152
PRM329 Premature Aging 36 2.178
153
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.164
154
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.164
155
P ATX030 Ataxia-Telangiectasia 80 2.164
156
TLN003 Telangiectasis 51 2.164
157
P BNG032 Benign Mesothelioma 53 2.164
158
P NRP001 Neuropathy 60 2.115
159
P PRP019 Peripheral Nervous System Disease 58 2.115
160
P DRR001 Diarrhea 55 2.100
161
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.098
162
ADL002 Adult Syndrome 70 2.098
163
c HPT003 Hepatitis a 63 2.070
164
P PRS040 Prostate Cancer 95 2.053
165
c PCH010 Pachyonychia Congenita 3 43 2.032
166
DVR002 Diverticulitis 46 2.032
167
CRN030 Coronary Stenosis 50 2.032
168
HRT011 Heart Septal Defect 49 2.032
169
CNS004 Constipation 56 2.032
170
P ATR010 Atrial Heart Septal Defect 58 2.032
171
GST045 Gastroenteritis 58 2.032
172
CRB086 Cerebral Aneurysms 40 2.032
173
ENT016 Enterovesical Fistula 19 2.032
174
PLC005 Placental Insufficiency 56 2.026
175
PLM033 Pulmonary Embolism 58 2.026
176
c ACT027 Acute Pancreatitis 60 2.020
177
P PRC031 Preeclampsia/eclampsia 1 43 1.985
178
TRM010 Traumatic Brain Injury 51 1.962
179
INS001 Insulinoma 59 1.962
180
P CRD119 Cardiac Arrest 67 1.962
181
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.946
182
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.943
183
P GST044 Gastritis 55 1.888
184
P PRL003 Proliferative Glomerulonephritis 43 1.888
185
P MYC008 Myocarditis 59 1.888
186
HDN002 Head Injury 44 1.888
187
MYT011 Myotonia 39 1.888
188
P DRM010 Dermatomyositis 61 1.854
189
P GRF003 Graft-Versus-Host Disease 71 1.854
190
c BLD140 Blood Group, I System 46 1.848
191
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.848
192
AGN016 Aging 54 1.833
193
P TRN020 Turner Syndrome 67 1.833
194
c ACT134 Acute Liver Failure 59 1.810
195
MRF001 Marfan Syndrome 76 1.810
196
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.810
197
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.810
198
ALL006 Allergic Asthma 56 1.810
199
GLL048 Glial Tumor 52 1.810
200
CHL147 Chlamydia Pneumonia 47 1.810
201
CLN015 Colon Adenocarcinoma 65 1.810
202
CHL123 Chlamydia 58 1.810
203
GLM045 Glioma 63 1.810
204
DFC004 Deficiency Anemia 74 1.781
206
THR024 Thrombosis 56 1.757
207
P PLY041 Polymyositis 59 1.757
208
c CHR417 Chronic Graft Versus Host Disease 55 1.757
209
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.727
210
P AVS003 Avascular Necrosis 41 1.727
211
RST023 Resting Heart Rate, Variation in 40 1.727
212
P KLZ004 Kala-Azar 1 41 1.727
213
DBN001 Dubin-Johnson Syndrome 57 1.727
214
LSH001 Leishmaniasis 64 1.727
215
P CND004 Candidiasis 58 1.727
216
P THY032 Thyroiditis 57 1.727
217
P MMB011 Membranous Nephropathy 50 1.727
218
BLR008 Bilirubin Metabolic Disorder 57 1.727
219
P ADN016 Adenocarcinoma 63 1.727
220
NPH010 Nephrosclerosis 50 1.727
221
P INF032 Infertility 57 1.727
222
CRT015 Carotid Artery Occlusion 45 1.727
223
P ADL010 Adult Respiratory Distress Syndrome 71 1.727
224
DFC001 Defective Apolipoprotein B-100 24 1.727
225
LMN011 Laminopathy 34 1.699
226
c LKM070 Leukemia, Acute Monocytic 56 1.699
227
ERY051 Erythroleukemia, Familial 37 1.699
228
ACT250 Acute Megakaryocytic Leukemia 60 1.699
229
PSY004 Psychotic Disorder 66 1.699
230
SCH003 Schizophreniform Disorder 55 1.699
231
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.699
232
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 1.699
233
AND005 Androgen Insensitivity Syndrome, Mild 21 1.699
234
c CHR064 Chronic Monocytic Leukemia 36 1.699
235
ATM095 Autoimmune Disease 61 1.642
236
c TYP008 Type 1 Diabetes Mellitus 70 1.638
237
HYP025 Hyperphosphatemia 48 1.638
238
P PNC035 Pancreatic Cancer 86 1.638
239
HPT004 Hepatic Coma 43 1.638
240
SCR011 Scrapie 39 1.638
241
CHR074 Choriocarcinoma 46 1.638
242
HRT012 Heart Valve Disease 53 1.638
243
HPT019 Hepatic Encephalopathy 59 1.638
244
DSS009 Disseminated Intravascular Coagulation 57 1.638
245
PRP030 Purpura 54 1.638
246
P ENC018 Encephalopathy 62 1.638
247
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 1.635
248
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.635
249
END072 Endotheliitis 36 1.620
250
MYL069 Myeloma, Multiple 77 1.548
251
P HPT021 Hepatitis 69 1.547
252
RDT013 Radiation Proctitis 48 1.540
253
LMB062 Limb Ischemia 55 1.540
254
P URN019 Urinary Tract Infection 49 1.540
255
ART074 Aortic Dissection 53 1.540
256
P PRP034 Purpura Fulminans 41 1.540
257
HRN029 Hearing Loss, Noise-Induced 37 1.540
258
P STS003 Sitosterolemia 53 1.540
259
P MSC003 Muscular Atrophy 52 1.540
260
ULC004 Ulcerative Colitis 74 1.540
261
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.540
262
P SNS001 Sensorineural Hearing Loss 59 1.540
263
c ACT068 Acute Cystitis 61 1.540
264
PRT018 Portal Vein Thrombosis 50 1.540
265
PRC003 Proctitis 49 1.540
266
DST006 Diastolic Heart Failure 45 1.540
268
DYS073 Dysphagia 53 1.540
269
c HYP839 Hyperlipidemia, Familial Combined, 1 30 1.524
270
FBR016 Fibrosclerosis of Breast 26 1.524
271
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.510
272
PST021 Postpartum Depression 50 1.501
273
CNG506 Congenital Amyoplasia 27 1.501
274
c PNS012 Paine Syndrome 60 1.501
275
c ART144 Arthrogryposis, Distal, Type 1a 60 1.501
276
P DST002 Distal Arthrogryposis 65 1.501
277
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.501
278
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.501
279
NTR005 Nutritional Deficiency Disease 61 1.501
280
MNT002 Mental Depression 57 1.501
281
ALK024 Alkuraya-Kucinskas Syndrome 45 1.501
282
DPR016 Depression 65 1.501
283
CYT018 Cytochrome P450 2d6 Variant 26 1.501
284
ACQ007 Acquired Immunodeficiency Syndrome 59 1.479
285
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.433
286
HYP540 Hypertension, Diastolic 37 1.433
287
HSH003 Hashimoto Thyroiditis 60 1.433
288
P PSR002 Psoriasis 63 1.433
289
P VSC011 Vasculitis 61 1.433
290
PST011 Pustulosis of Palm and Sole 52 1.433
291
c CRN178 Coronary Heart Disease 6 18 1.433
292
ALL029 Allergic Disease 59 1.433
293
ING001 Inguinal Hernia 59 1.433
294
SQM006 Squamous Cell Carcinoma 60 1.433
295
HLL004 Hellp Syndrome 53 1.433
296
HYP555 Hypertriglyceridemia, Transient Infantile 38 1.427
297
P RHB003 Rhabdomyosarcoma 66 1.366
298
P DMN002 Dementia 66 1.366
299
RFR010 Refractory Anemia 49 1.326
300
SDD004 Sudden Arrhythmia Death Syndrome 22 1.326
301
c MCL062 Mucolipidosis Ii Alpha/beta 68 1.326
302
ANX010 Anxiety 70 1.326
303
P MLT020 Multiple Sclerosis 79 1.326
304
CRH005 Crohn's Colitis 53 1.326
305
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.326
306
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.326
307
c INF071 Inflammatory Bowel Disease 1 65 1.326
308
CMR002 Coumarin Resistance 59 1.326
309
JVN004 Juvenile Myelomonocytic Leukemia 67 1.326
310
ATN013 Autoinflammation, Panniculitis, and Dermatosis Syndrome 49 1.326
311
P CHR285 Chronic Myelomonocytic Leukemia 60 1.326
312
CRH001 Crohn's Disease 80 1.326
313
BNM001 Bone Marrow Cancer 46 1.326
314
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 1.326
315
PLM001 Pulmonary Tuberculosis 69 1.326
316
LNG031 Lung Benign Neoplasm 51 1.326
317
CHL061 Childhood Leukemia 47 1.326
318
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.326
319
MYL031 Myeloproliferative Neoplasm 66 1.326
320
ADL096 Adult Hepatocellular Carcinoma 60 1.326
321
KRT002 Keratomalacia 55 1.326
322
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.326
323
c MGR028 Migraine with or Without Aura 1 64 1.311
324
c MYC058 Myocardial Infarction 2 24 1.311
325
P SRC025 Sarcoidosis 1 71 1.311
326
SKN016 Skin Disease 63 1.311
327
PRM236 Primary Biliary Cholangitis 60 1.311
328
P BND020 Bone Disease 59 1.311
329
STM007 Stomatitis 54 1.311
330
c HRM017 Hermansky-Pudlak Syndrome 2 55 1.304
331
ADN018 Adenoma 59 1.288
332
P END044 Endometriosis 62 1.211
333
P EMB005 Embryonal Rhabdomyosarcoma 53 1.205
334
P PRP003 Porphyria Cutanea Tarda 66 1.194
335
BRN012 Bronchiolitis Obliterans 56 1.194
336
BRN002 Bronchiolitis 57 1.194
337
P PRP029 Porphyria 60 1.194
338
THR123 Thrombotic Microangiopathy 40 1.166
339
OST159 Osteogenic Sarcoma 66 1.166
340
P PRK001 Porokeratosis 55 1.166
341
P ART023 Arthropathy 61 1.166
342
EXT034 Extrinsic Allergic Alveolitis 57 1.166
343
P PLY019 Polyneuropathy 52 1.166
344
MNN017 Mononeuropathy 41 1.166
345
P ACT105 Acute Mountain Sickness 52 1.166
346
P HDC001 Headache 57 1.166
348
HYP732 Hyperalphalipoproteinemia 1 52 1.115
349
GTR002 Goiter 53 1.115
350
SVR004 Severe Combined Immunodeficiency 72 1.115
351
P RHN004 Rhinitis 57 1.115
352
P SLP005 Sleep Disorder 61 1.115
353
P HYP076 Hyperthyroidism 53 1.115
354
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 52 1.024
355
P PRS038 Personality Disorder 65 1.024
356
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.018
357
P OVR042 Ovarian Cancer 88 1.018
358
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.018
359
HYP457 Hypertrophic Scars 42 1.018
360
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 1.018
361
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.018
362
P BCL017 B-Cell Lymphoma 59 1.018
363
P LTR001 Lateral Sclerosis 58 1.018
364
P PLY011 Polycystic Ovary Syndrome 57 1.018
365
PHR003 Pharyngitis 58 1.018
366
P HYP121 Hypoalphalipoproteinemia 43 1.018
367
VSC002 Vascular Dementia 60 1.018
368
c SCL052 Scleroderma, Familial Progressive 61 0.978
369
P PRG092 Pregnancy Loss, Recurrent 1 41 0.978
370
P ICH004 Ichthyosis 56 0.978
371
MST021 Meester-Loeys Syndrome 42 0.911
372
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.911
373
c MJR022 Major Affective Disorder 8 38 0.911
374
HPT046 Hepatic Veno-Occlusive Disease 62 0.911
375
c MJR024 Major Affective Disorder 9 41 0.911
376
CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.911
377
BCT022 Bacterial Infectious Disease 56 0.911
378
P ALP008 Alopecia 54 0.911
379
47X002 47,xyy 48 0.911
380
P THR014 Thrombocytopenia 66 0.911
381
P BPL003 Bipolar Disorder 56 0.911
382
P SKN015 Skin Carcinoma 71 0.911
383
LNG099 Lung Disease 62 0.911
384
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.911
385
SBC019 Subcutaneous Mycosis 35 0.911
386
SPR010 Sporotrichosis 46 0.911
387
P RNL015 Renal Hypertension 45 0.911
388
P MYG005 Myoglobinuria 40 0.911
389
HYP014 Hyperuricemia 51 0.911
390
RHB024 Rhabdomyosarcoma 2 67 0.904
391
AMD002 Amed Syndrome, Digenic 37 0.904
392
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.849
393
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.849
394
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.849
395
c SYS043 Systemic Lupus Erythematosus 1 38 0.849
396
P FNG006 Feingold Syndrome 1 62 0.849
397
P OCL002 Oculocutaneous Albinism 59 0.849
398
c HRM012 Hermansky-Pudlak Syndrome 9 45 0.849
399
MSC007 Muscle Hypertrophy 64 0.849
400
P LYM118 Lymphoma 67 0.849
401
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.849
402
c PRS136 Prostate Cancer, Hereditary, 6 33 0.849
403
c HRM006 Hermansky-Pudlak Syndrome 3 44 0.849
404
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.849
405
c HRM008 Hermansky-Pudlak Syndrome 5 47 0.849
406
c HRM009 Hermansky-Pudlak Syndrome 6 45 0.849
407
c HRM010 Hermansky-Pudlak Syndrome 7 38 0.849
408
c HRM011 Hermansky-Pudlak Syndrome 8 35 0.849
409
DWN001 Down Syndrome 70 0.849
410
STR089 Storage Pool Platelet Disease 47 0.849
411
APR006 Apert Syndrome 70 0.849
412
c PRS130 Prostate Cancer, Hereditary, 8 32 0.849
413
PRS047 Prostatitis 58 0.849
414
P HRM001 Hermansky-Pudlak Syndrome 65 0.849
415
HYP005 Hypokalemia 55 0.849
416
IDP011 Idiopathic Interstitial Pneumonia 59 0.849
417
ALB002 Albinism 47 0.849
418
c CRD027 Cardiomyopathy Due to Anthracyclines 9 0.849
419
LYM019 Lymphosarcoma 46 0.849
420
HMN044 Human Immunodeficiency Virus Type 1 78 0.845
421
CRT045 Creatine Phosphokinase, Elevated Serum 39 0.789
422
c THR092 Thrombophilia Due to Thrombin Defect 74 0.789
423
P PRK057 Parkinson Disease, Late-Onset 80 0.789
424
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.789
425
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.789
426
LPP002 Lipoprotein Glomerulopathy 43 0.789
427
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.789
428
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.789
429
P OPN001 Open-Angle Glaucoma 55 0.789
430
GSG001 Gas Gangrene 52 0.789
431
OST012 Osteoarthritis 77 0.789
432
CMB007 Combined Immunodeficiency 57 0.789
433
CHL004 Cholelithiasis 49 0.789
434
c DLT002 Dilated Cardiomyopathy 78 0.789
435
RTN003 Retinal Ischemia 49 0.789
436
IMP005 Impotence 52 0.789
437
GST033 Gestational Diabetes 61 0.789
438
P PRN023 Prion Disease 60 0.789
439
P RTN018 Retinal Disease 53 0.789
440
SBC016 Subacute Delirium 43 0.789
441
SRT004 Serotonin Syndrome 54 0.644
442
P SZR006 Seizure Disorder 70 0.644
443
c THY107 Thymoma, Familial 42 0.644
444
END057 Endometrial Cancer 72 0.644
445
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.644
446
P FML012 Familial Partial Lipodystrophy 54 0.644
447
P MLT008 Multinodular Goiter 42 0.644
448
FRS012 First-Degree Atrioventricular Block 39 0.644
449
ATR057 Atrioventricular Block 54 0.644
450
BRR014 Barrett Esophagus 66 0.644
451
PLY179 Polyomavirus-Associated Nephropathy 25 0.644
452
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.644
453
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.644
454
VRC005 Varicose Veins 60 0.644
455
OCL069 Ocular Motor Apraxia 57 0.644
456
P RTN024 Retinoblastoma 73 0.644
457
c NMN015 Niemann-Pick Disease, Type C1 68 0.644
458
c LPD015 Lipodystrophy, Familial Partial, Type 2 61 0.644
459
RNL077 Renal Fibrosis 46 0.644
460
P LCH002 Lichen Planus 54 0.644
461
ADG002 Audiogenic Seizures 25 0.644
462
P ALC033 Alcohol Use Disorder 61 0.644
463
PNC129 Pancreatic Adenocarcinoma 65 0.644
464
GLB002 Glioblastoma 67 0.644
465
ADR005 Adrenal Carcinoma 62 0.644
466
FLL031 Follicular Adenoma 40 0.644
467
ILS001 Ileus 50 0.644
468
PRL008 Paralytic Ileus 45 0.644
469
P CTR002 Cataract 60 0.644
470
P MNC007 Monocytic Leukemia 47 0.644
471
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.644
472
ERY003 Erythema Multiforme 56 0.644
473
LFT001 Left Bundle Branch Hemiblock 47 0.644
474
P NMN002 Niemann-Pick Disease 60 0.644
475
NRL004 Neuroleptic Malignant Syndrome 52 0.644
476
P THY023 Thymoma 64 0.644
477
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.644
478
RGH001 Right Bundle Branch Block 47 0.644
479
HYP056 Hypoglycemia 65 0.644
480
BRN071 Brain Injury 50 0.644
481
HMP009 Haemophilus Influenzae 41 0.644
482
GYN001 Gynecomastia 47 0.522
483
P MTC133 Mitochondrial Myopathy 50 0.522
484
IND009 Indeterminate Cell Histiocytosis 20 0.522
485
HST010 Histiocytosis 49 0.522
486
INF021 Infant Gynecomastia 30 0.522
487
CRT004 Carotid Artery Thrombosis 39 0.522
488
c ICH023 Ichthyosis, Acquired 30 0.522
489
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.455
490
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.455
491
RCK009 Rickettsial Disease 18 0.455
492
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.455
493
MTH071 Methane Production 25 0.455
494
INS024 Insulin-Like Growth Factor I 78 0.455
495
SHR107 Short Stature-Obesity Syndrome 25 0.455
496
CRD223 Cardiac Arrhythmia 63 0.455
497
MYC006 Mycosis Fungoides 65 0.455
498
TNG002 Tangier Disease 64 0.455
499
ALL003 Allergic Rhinitis 67 0.455
500
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.455
501
HMC014 Homocysteinemia 52 0.455
502
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.455
503
P PHC003 Pheochromocytoma 69 0.455
504
P LKM071 Leukemia, Chronic Lymphocytic 75 0.455
505
P CLR023 Colorectal Cancer 100 0.455
506
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.455
507
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.455
508
TND004 Tendinopathy 45 0.455
509
ADR016 Adrenal Cortical Carcinoma 62 0.455
510
MNT001 Mantle Cell Lymphoma 67 0.455
511
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.455
512
INV001 Invasive Aspergillosis 49 0.455
513
TND005 Tendinitis 54 0.455
514
INF034 Infective Endocarditis 54 0.455
515
HMN047 Human Cytomegalovirus Infection 57 0.455
516
SXL003 Sexual Disorder 49 0.455
517
LYS012 Lysosomal Acid Lipase Deficiency 65 0.455
518
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.455
519
P ASP006 Aspergillosis 72 0.455
520
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.455
521
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.455
522
VTR016 Vater/vacterl Association 49 0.455
523
c HYP837 Hypercholesterolemia, Familial, 2 46 0.455
525
GST019 Gastrointestinal Stromal Tumor 78 0.455
526
c NMN014 Niemann-Pick Disease, Type C2 49 0.455
527
DSS032 Disease by Infectious Agent 55 0.455
528
ADR040 Adrenal Gland Pheochromocytoma 46 0.455
529
CHR431 Chronic Venous Insufficiency 48 0.455
530
CRD137 Cardiogenic Shock 56 0.455
532
c HYP843 Hypoalphalipoproteinemia, Primary, 2 50 0.455
533
PMP014 Pemphigoid 51 0.455
534
PRT037 Pertussis 65 0.455
535
P PRK039 Parkinsonism 55 0.455
536
URM002 Uremia 47 0.455
537
URT010 Ureteral Obstruction 45 0.455
538
SPC005 Speech Disorder 45 0.455
539
RSC001 Rosacea 55 0.455
540
P HRP006 Herpes Simplex 65 0.455
541
P MLG056 Malignant Hyperthermia 66 0.455
542
SYS071 Systemic Autoimmune Disease 35 0.455
543
P ALP009 Alopecia Areata 59 0.455
544
INT002 Intermittent Claudication 61 0.455
545
ADR004 Adrenal Cortical Adenocarcinoma 38 0.455
546
P EPL164 Epilepsy 68 0.455
547
P FBR017 Fibrosarcoma 56 0.455
548
P BRS044 Breast Adenocarcinoma 58 0.455
549
c HRD002 Hereditary Angioedema 62 0.455
550
P ACN011 Acne 57 0.455
551
P RTN016 Retinal Degeneration 52 0.455
552
PPT005 Peptic Ulcer Disease 58 0.455
553
P PLY020 Polyradiculoneuropathy 46 0.455
554
BLL006 Bullous Pemphigoid 61 0.455
555
P VNS003 Venous Insufficiency 55 0.455
556
SPP007 Suppression Amblyopia 38 0.455
557
AMB002 Amblyopia 50 0.455
558
NSP002 Nasopharyngitis 45 0.455
559
P CTN003 Cutaneous Lupus Erythematosus 52 0.455
560
ANG020 Angiosarcoma 64 0.455
561
P DNG005 Dengue Virus 56 0.455
562
P MGR001 Migraine Without Aura 49 0.455
563
CRN019 Coronary Artery Vasospasm 47 0.455
564
CRN017 Coronary Thrombosis 46 0.455
565
P HYP061 Hypertrophic Cardiomyopathy 69 0.455
566
P GRV001 Graves' Disease 55 0.455
567
P GLL022 Guillain-Barre Syndrome 60 0.455
568
HRY003 Hairy Cell Leukemia 61 0.455
569
THY122 Thyroid Gland Cancer 59 0.455
570
P MLN008 Melanoma 76 0.455
571
RTN020 Retinal Vascular Disease 46 0.455
572
CHL014 Cholera 62 0.455
573
P ANG015 Angioedema 56 0.455
574
KRT009 Keratosis 53 0.455
575
P ESS003 Essential Thrombocythemia 69 0.455
576
HGH043 High Grade Glioma 45 0.455
577
SCH014 Schistosomiasis 56 0.455
578
P HYD006 Hydrocephalus 61 0.455
579
HMP005 Hemiplegia 54 0.455
580
MTR002 Mitral Valve Insufficiency 52 0.455
581
P END033 Endocarditis 58 0.455
582
ADJ001 Adjustment Disorder 47 0.455
583
ART008 Arteriosclerosis Obliterans 40 0.455
584
P OVR046 Ovarian Cyst 46 0.455
585
ACT058 Active Peptic Ulcer Disease 56 0.455
586
EMB004 Embryonal Carcinoma 56 0.455
587
P CYS039 Cystic Kidney Disease 53 0.455
588
P KDN017 Kidney Cancer 61 0.455
589
P MTR014 Motor Neuron Disease 65 0.455
590
DRM006 Dermatitis 62 0.455
591
BRS051 Breast Disease 58 0.455
592
BLT003 Blue Toe Syndrome 24 0.455
593
BNG018 Benign Paroxysmal Positional Nystagmus 41 0.455
594
VCT001 Vacterl Association 47 0.455
595
P URT039 Urticaria 58 0.455
596
P NRM002 Normal Pressure Hydrocephalus 49 0.455
597
CRB033 Cerebral Degeneration 39 0.455
598
c HPT016 Hepatitis B 62 0.455
599
CLC006 Calcinosis 47 0.455
600
STT001 Status Epilepticus 59 0.455
601
PST028 Post-Traumatic Stress Disorder 59 0.455
602
P INS002 in Situ Carcinoma 53 0.455
603
P CMP008 Compartment Syndrome 50 0.455
604
DCB001 Decubitus Ulcer 62 0.455
605
HPR003 Heparin-Induced Thrombocytopenia 47 0.455
606
NCR015 Necrotizing Autoimmune Myopathy 27 0.455
607
ORL011 Oral Cancer 60 0.455
608
CRY036 Cryptogenic Cirrhosis 36 0.455
609
PTT037 Pituitary Tumors 44 0.455
610
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.455
611
CND006 Candida Glabrata 30 0.455
612
APD001 Apo a-I Deficiency 16 0.455
613
KSH003 Kshv Inflammatory Cytokine Syndrome 16 0.455
614
LCH008 Lichen Planus Pigmentosus 23 0.455
615
FRN020 Frontal Fibrosing Alopecia 48 0.455
616
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.426
617
ASP030 Aspirin Resistance 40 0.426
618
CMP010 Complex Regional Pain Syndrome 60 0.426
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