Search results for Amlodipine

414 hits were found for Amlodipine

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 1.111
2
ANG054 Angina Pectoris 66 0.328
3
LPD008 Lipid Metabolism Disorder 62 0.300
4
LPP008 Lipoprotein Quantitative Trait Locus 62 0.263
5
P KDN018 Kidney Disease 72 0.259
6
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.257
7
P CRD246 Cardiovascular System Disease 57 0.247
8
c FML035 Familial Hyperlipidemia 55 0.247
9
CNG034 Congestive Heart Failure 69 0.234
10
CRB039 Cerebrovascular Disease 67 0.234
11
P CRN300 Coronary Heart Disease 1 63 0.232
12
P HRT032 Heart Disease 75 0.225
13
ART140 Arteries, Anomalies of 52 0.223
14
STR067 Stroke, Ischemic 81 0.220
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.215
16
c CHR684 Chronic Kidney Disease 70 0.215
17
HYP005 Hypokalemia 55 0.213
18
ADL002 Adult Syndrome 70 0.211
19
GNG012 Gingival Overgrowth 51 0.211
20
P DBT009 Diabetes Mellitus 64 0.190
21
ISC004 Ischemia 58 0.190
22
c HYP836 Hypercholesterolemia, Familial, 1 73 0.179
23
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.173
24
P OVR082 Overgrowth Syndrome 50 0.173
25
ATH013 Atherosclerosis Susceptibility 65 0.170
26
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.170
27
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.170
28
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.170
29
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.170
30
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.170
31
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.170
32
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.170
33
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.170
34
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.170
35
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.170
36
48X005 48,xyyy 39 0.170
37
P TRN020 Turner Syndrome 67 0.167
38
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.164
39
HYP540 Hypertension, Diastolic 40 0.164
40
P MYC007 Myocardial Infarction 70 0.161
41
MSC007 Muscle Hypertrophy 64 0.157
42
c RHB024 Rhabdomyosarcoma 2 67 0.151
43
P VSC007 Vascular Disease 63 0.147
44
c MCR113 Microvascular Complications of Diabetes 3 52 0.147
45
c MCR120 Microvascular Complications of Diabetes 7 47 0.147
46
c MCR130 Microvascular Complications of Diabetes 6 41 0.147
47
c MCR133 Microvascular Complications of Diabetes 4 41 0.147
48
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.136
49
HMS001 Hemosiderosis 54 0.132
50
HYP081 Hypolipoproteinemia 51 0.132
51
P RRH023 Rare Hereditary Hemochromatosis 41 0.132
52
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.128
53
PLM010 Pulmonary Edema 54 0.128
54
END086 End Stage Renal Disease 51 0.128
55
NTR005 Nutritional Deficiency Disease 62 0.124
56
P THL005 Thalassemia 60 0.124
57
c HYP272 Hypercholesterolemia, Familial, 3 44 0.124
58
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.120
59
DWN001 Down Syndrome 70 0.116
60
P MCR115 Microvascular Complications of Diabetes 5 66 0.116
61
P ATR011 Atrial Fibrillation 66 0.116
62
c FML001 Familial Atrial Fibrillation 65 0.116
63
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.116
64
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.116
65
LPT014 Leptin Deficiency or Dysfunction 74 0.107
66
PRP027 Peripheral Vascular Disease 71 0.107
67
c ALP101 Alpha-Thalassemia 62 0.107
68
IRN002 Iron Metabolism Disease 57 0.107
69
P HDC001 Headache 57 0.107
70
INT007 Intermediate Coronary Syndrome 55 0.107
71
P DMN002 Dementia 66 0.102
72
c MCR129 Microvascular Complications of Diabetes 1 66 0.102
73
ATX019 Ataxia with Vitamin E Deficiency 42 0.102
74
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.102
75
OST012 Osteoarthritis 78 0.096
76
c BTT014 Beta-Thalassemia 74 0.096
77
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.096
78
KHL003 Kohlschutter-Tonz Syndrome 65 0.096
79
HYP060 Hyperinsulinism 54 0.096
80
HMC014 Homocysteinemia 53 0.096
81
c DLT002 Dilated Cardiomyopathy 79 0.091
82
ANX010 Anxiety 73 0.091
83
P LVR013 Liver Disease 68 0.091
84
PRT058 Pure Autonomic Failure 59 0.091
85
GLC003 Glucose Intolerance 54 0.091
86
HYP014 Hyperuricemia 52 0.091
87
c MCR112 Microvascular Complications of Diabetes 2 41 0.091
88
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.085
89
P SLP006 Sleep Apnea 69 0.085
90
P CRD119 Cardiac Arrest 67 0.085
91
CRD132 Cardiac Conduction Defect 58 0.085
92
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.085
93
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.085
94
c ATR087 Atrial Standstill 1 75 0.079
95
ANR040 Aneurysm 59 0.079
96
CNS004 Constipation 58 0.079
97
c ACT075 Acute Myocardial Infarction 57 0.079
98
IMP005 Impotence 52 0.079
99
NPH010 Nephrosclerosis 50 0.079
100
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.072
101
P MYP004 Myopathy 70 0.072
102
ART016 Aortic Aneurysm 69 0.072
103
APN008 Apnea, Obstructive Sleep 64 0.072
104
GT001 Gout 64 0.072
105
c PRC016 Pre-Eclampsia 63 0.072
106
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.072
107
P HYP750 Hypertriglyceridemia, Familial 62 0.072
108
P VSC011 Vasculitis 62 0.072
109
ALL026 Allergic Hypersensitivity Disease 62 0.072
110
FTT001 Fatty Liver Disease 61 0.072
111
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.072
112
VSL002 Visual Epilepsy 59 0.072
113
GLS018 Glass Syndrome 57 0.072
114
P EXN002 Exanthem 57 0.072
115
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.072
116
VSC002 Vascular Dementia 57 0.072
117
HMR039 Hemorrhage, Intracerebral 57 0.072
118
HYP266 Hypoxia 57 0.072
119
P ANG015 Angioedema 57 0.072
120
P SZR006 Seizure Disorder 56 0.072
121
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.072
122
P ART021 Arteriosclerosis 54 0.072
123
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.072
124
PRP080 Peripheral Artery Disease 53 0.072
125
TLN003 Telangiectasis 52 0.072
126
MTB004 Metabolic Acidosis 50 0.072
127
47X002 47,xyy 49 0.072
128
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.072
129
DST006 Diastolic Heart Failure 45 0.072
130
RST023 Resting Heart Rate, Variation in 41 0.072
131
CYT018 Cytochrome P450 2d6 Variant 27 0.072
132
c ART115 Aortic Valve Disease 1 75 0.064
133
P RSP003 Respiratory Failure 74 0.064
134
c PNC108 Pancreatitis, Hereditary 70 0.064
135
P THR014 Thrombocytopenia 67 0.064
136
P HPT021 Hepatitis 67 0.064
137
P PLM037 Pulmonary Hypertension 67 0.064
138
c MGR028 Migraine with or Without Aura 1 67 0.064
139
P DYS154 Dystonia 65 0.064
140
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.064
141
c ART101 Aortic Valve Disease 2 65 0.064
142
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.064
143
TRN015 Transient Cerebral Ischemia 63 0.064
144
DPR016 Depression 63 0.064
145
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.064
146
P PNC044 Pancreatitis 61 0.064
147
c ACT027 Acute Pancreatitis 60 0.064
148
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.064
149
MNT002 Mental Depression 58 0.064
150
P GST044 Gastritis 56 0.064
151
P ART018 Aortic Valve Insufficiency 49 0.064
152
URM002 Uremia 49 0.064
153
CLC006 Calcinosis 48 0.064
154
P RNV001 Renovascular Hypertension 48 0.064
155
LPT006 Leptin Receptor Deficiency 48 0.064
156
P RNL015 Renal Hypertension 47 0.064
157
RYN005 Raynaud Phenomenon 47 0.064
158
SYN036 Syncope 45 0.064
159
P SDR002 Siderosis 44 0.064
160
NSP002 Nasopharyngitis 43 0.064
161
49X006 49, Xxxxy Syndrome 41 0.064
162
P ALZ034 Alzheimer Disease 88 0.056
163
CNN003 Conn's Syndrome 79 0.056
164
P OST002 Osteoporosis 74 0.056
165
P CNR004 Cone-Rod Dystrophy 2 73 0.056
166
DFC004 Deficiency Anemia 70 0.056
167
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.056
168
BRN024 Bronchitis 68 0.056
169
PNC129 Pancreatic Adenocarcinoma 68 0.056
170
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.056
171
c FML021 Familial Hypercholesterolemia 66 0.056
172
HYP056 Hypoglycemia 66 0.056
173
c DBT099 Diabetes Mellitus, Type I 65 0.056
174
PRP083 Porphyria, Acute Intermittent 64 0.056
175
P ADN016 Adenocarcinoma 64 0.056
176
c HPT001 Hepatitis C 62 0.056
177
c DYS056 Dystonia 12 62 0.056
178
BLL006 Bullous Pemphigoid 62 0.056
179
P PRP029 Porphyria 62 0.056
180
HYP066 Hyperglycemia 61 0.056
181
P NPH012 Nephrotic Syndrome 60 0.056
182
TRG002 Trigeminal Neuralgia 60 0.056
183
P OPT006 Optic Nerve Disease 60 0.056
184
P MYC008 Myocarditis 59 0.056
185
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.056
186
EYD002 Eye Disease 58 0.056
187
P INF032 Infertility 57 0.056
188
P GLM007 Glomerulonephritis 57 0.056
189
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.056
190
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 57 0.056
191
MCL006 Macular Retinal Edema 55 0.056
192
PRP030 Purpura 54 0.056
193
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.056
194
GST023 Gastric Ulcer 53 0.056
195
P RTN018 Retinal Disease 53 0.056
196
CRT013 Carotid Stenosis 50 0.056
197
BRN071 Brain Injury 49 0.056
198
CCN001 Cocaine Dependence 48 0.056
199
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.056
200
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.056
201
P TRT019 Torticollis 48 0.056
202
SXL003 Sexual Disorder 47 0.056
203
c MLG069 Malignant Hypertension 47 0.056
204
RNL077 Renal Fibrosis 47 0.056
205
ANV001 Anovulation 47 0.056
206
CRB004 Cerebral Artery Occlusion 45 0.056
207
P OCY003 Oocyte Maturation Defect 1 45 0.056
208
CRB008 Cerebral Atherosclerosis 44 0.056
209
IDP033 Idiopathic Edema 44 0.056
210
CRV043 Cervical Dystonia 42 0.056
211
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.056
212
c CTR132 Cataract 3, Multiple Types 41 0.056
213
FCL022 Focal Dystonia 41 0.056
214
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.056
215
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.056
216
c CHR682 Chronic Bilirubin Encephalopathy 39 0.056
217
GNG006 Gingival Hypertrophy 34 0.056
218
DYS198 Dystonia, Focal, Task-Specific 32 0.056
219
VLK001 Volkmann Contracture 25 0.056
220
P BRS047 Breast Cancer 97 0.045
221
P NRB001 Neuroblastoma 72 0.045
222
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.045
223
P ART022 Arthritis 69 0.045
224
P LKM002 Leukemia 68 0.045
225
c HYP768 Hyperlipoproteinemia, Type I 67 0.045
226
PSY004 Psychotic Disorder 67 0.045
227
ALC007 Alcohol Dependence 66 0.045
228
P NTR004 Neutropenia 63 0.045
229
P PLY014 Polycystic Kidney Disease 62 0.045
230
c SVR001 Severe Acute Respiratory Syndrome 62 0.045
231
LVR012 Liver Cirrhosis 62 0.045
232
P LPS004 Lupus Erythematosus 61 0.045
233
P SLP005 Sleep Disorder 59 0.045
234
ADN018 Adenoma 59 0.045
235
P ALC033 Alcohol Use Disorder 58 0.045
236
DSS008 Disease of Mental Health 58 0.045
237
LST001 Listeriosis 56 0.045
238
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.045
239
P PNM006 Pneumoconiosis 56 0.045
240
AGN016 Aging 56 0.045
241
ATR057 Atrioventricular Block 55 0.045
242
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.045
243
OCL020 Ocular Cicatricial Pemphigoid 55 0.045
244
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.045
245
END040 Endogenous Depression 55 0.045
246
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.045
247
P LCH002 Lichen Planus 53 0.045
248
RHM028 Rheumatic Heart Disease 53 0.045
249
NRT001 Neurotic Disorder 53 0.045
250
SYS003 Systolic Heart Failure 49 0.045
251
RYN001 Raynaud Disease 48 0.045
252
INT067 Interstitial Nephritis 48 0.045
253
c MTR002 Mitral Valve Insufficiency 48 0.045
254
ANT018 Anthracosis 48 0.045
255
MYC005 Myocardial Stunning 46 0.045
256
SBC016 Subacute Delirium 44 0.045
257
PPL001 Papillary Adenoma 44 0.045
258
CVD001 Covid-19 44 0.045
259
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.045
260
TRP009 Triple X Syndrome 42 0.045
261
PRS063 Paresthesia 41 0.045
262
ALD013 Aldosterone-Producing Adenoma 39 0.045
263
HYP114 Hypertensive Nephropathy 36 0.045
264
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.045
265
ADR057 Adrenogenital Syndrome 32 0.045
266
RNL001 Renal Artery Obstruction 31 0.045
267
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.045
268
c SYS001 Systemic Lupus Erythematosus 86 0.032
269
P RHM011 Rheumatoid Arthritis 80 0.032
270
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.032
271
AST005 Asthma 76 0.032
272
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.032
273
SCK003 Sickle Cell Anemia 74 0.032
274
c HMC039 Hemochromatosis, Type 1 74 0.032
275
ULC004 Ulcerative Colitis 73 0.032
276
P RTN024 Retinoblastoma 73 0.032
277
c HPT073 Hepatitis C Virus 72 0.032
278
P GRF003 Graft-Versus-Host Disease 72 0.032
279
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.032
280
P PNM007 Pneumonia 68 0.032
281
c BSL007 Basal Cell Carcinoma 68 0.032
282
CNN005 Connective Tissue Disease 68 0.032
283
P ALP004 Alport Syndrome 68 0.032
284
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.032
285
P HYP098 Hypereosinophilic Syndrome 67 0.032
286
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.032
287
MYC006 Mycosis Fungoides 66 0.032
288
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.032
289
CHG001 Chagas Disease 66 0.032
290
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.032
291
IRR002 Irritable Bowel Syndrome 65 0.032
292
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.032
293
P PRD008 Periodontitis 64 0.032
294
LSH001 Leishmaniasis 63 0.032
295
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.032
296
c ACT068 Acute Cystitis 63 0.032
297
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.032
298
CLT003 Colitis 62 0.032
299
P PSR002 Psoriasis 62 0.032
300
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.032
301
ATM095 Autoimmune Disease 62 0.032
302
TXC005 Toxic Shock Syndrome 62 0.032
303
DRM006 Dermatitis 61 0.032
304
ALC006 Alcoholic Hepatitis 61 0.032
305
RTN017 Retinal Detachment 61 0.032
306
P MYL006 Myeloid Leukemia 60 0.032
307
INS001 Insulinoma 60 0.032
308
STT001 Status Epilepticus 60 0.032
309
PLM033 Pulmonary Embolism 59 0.032
310
P INT070 Intestinal Obstruction 58 0.032
311
ADR005 Adrenal Carcinoma 58 0.032
312
ERY003 Erythema Multiforme 58 0.032
313
P URT039 Urticaria 58 0.032
314
P MTR012 Mitral Valve Disease 58 0.032
315
c DWL002 Dowling-Degos Disease 1 58 0.032
316
P PRP019 Peripheral Nervous System Disease 58 0.032
317
P MYS005 Myositis 56 0.032
318
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.032
319
P PLY011 Polycystic Ovary Syndrome 56 0.032
320
P NRP001 Neuropathy 56 0.032
321
ALL001 Allan-Herndon-Dudley Syndrome 56 0.032
322
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.032
323
c GRV008 Graves Disease 1 56 0.032
324
MCS002 Mucositis 56 0.032
325
BRN004 Brain Edema 56 0.032
326
ADR008 Adrenal Adenoma 55 0.032
327
P MLN007 Male Infertility 55 0.032
328
VSC003 Visceral Leishmaniasis 55 0.032
329
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.032
330
P SLM003 Salmonellosis 55 0.032
331
AMN003 Amnestic Disorder 54 0.032
332
P ALP008 Alopecia 54 0.032
333
P INF037 Inflammatory Bowel Disease 54 0.032
334
AMN001 Amenorrhea 54 0.032
335
NNL006 Non-Alcoholic Steatohepatitis 54 0.032
336
PRS045 Prostatic Hypertrophy 53 0.032
337
GSG001 Gas Gangrene 53 0.032
338
INT075 Intracranial Hypertension 53 0.032
339
c FML008 Familial Retinoblastoma 53 0.032
340
PST011 Pustulosis of Palm and Sole 52 0.032
341
PNG002 Pain Agnosia 51 0.032
342
PRS021 Prostatic Adenoma 51 0.032
343
P ECL001 Eclampsia 50 0.032
344
CRN030 Coronary Stenosis 50 0.032
345
P SCK005 Sickle Cell Disease 50 0.032
346
BLR001 Biliary Atresia 50 0.032
347
P IGN003 Iga Nephropathy 1 49 0.032
348
HYP006 Hypertensive Heart Disease 49 0.032
349
GYN001 Gynecomastia 49 0.032
350
LFT001 Left Bundle Branch Hemiblock 49 0.032
351
PRS129 Prostatic Hyperplasia, Benign 49 0.032
352
INT078 Intracranial Thrombosis 49 0.032
353
P MGR001 Migraine Without Aura 49 0.032
354
c BCT013 Bacterial Pneumonia 48 0.032
355
BNR002 Bone Resorption Disease 48 0.032
356
WTH001 Withdrawal Disorder 48 0.032
357
ATS010 Autosomal Recessive Disease 48 0.032
358
IGG001 Iga Glomerulonephritis 48 0.032
359
ART004 Aortic Atherosclerosis 47 0.032
360
HLX001 Helix Syndrome 47 0.032
361
PRD004 Prediabetes Syndrome 47 0.032
362
CRN017 Coronary Thrombosis 47 0.032
363
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.032
364
TST044 Testicular Torsion 47 0.032
365
LPD004 Lipoid Nephrosis 46 0.032
366
CRN019 Coronary Artery Vasospasm 46 0.032
367
P MYC033 Myoclonus 46 0.032
368
ANR004 Anuria 46 0.032
369
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.032
370
c TRC022 Tricuspid Valve Insufficiency 45 0.032
371
URT010 Ureteral Obstruction 45 0.032
372
ORL013 Oral Lichen Planus 45 0.032
373
c NPH054 Nephrotic Syndrome, Type 3 45 0.032
374
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.032
375
URL001 Urolithiasis 45 0.032
376
CRT015 Carotid Artery Occlusion 45 0.032
377
IMM064 Immunodeficiency, Common Variable, 10 44 0.032
378
c PRM038 Primary Agammaglobulinemia 44 0.032
379
GRN007 Granuloma Annulare 44 0.032
380
CRB090 Cerebral Hypoxia 44 0.032
381
ADR041 Adrenal Cortical Adenoma 43 0.032
382
LMY003 Leiomyomatosis 43 0.032
383
LWC001 Low Compliance Bladder 43 0.032
384
PLY068 Polysubstance Abuse 43 0.032
385
CYT002 Cytokine Deficiency 42 0.032
386
c RTN047 Retinitis Pigmentosa 18 42 0.032
387
PHY002 Physical Disorder 42 0.032
388
P LBY004 Labyrinthitis 42 0.032
389
BCK006 Back Pain 42 0.032
390
P KLZ004 Kala-Azar 1 41 0.032
391
P HYP263 Hypersomnia 41 0.032
392
ACT088 Acute Insulin Response 41 0.032
393
RDN001 Reading Disorder 40 0.032
394
LNR006 Linear Iga Disease 40 0.032
395
CLP006 Clopidogrel Resistance 40 0.032
396
HYP008 Hypertensive Retinopathy 39 0.032
397
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.032
398
c HNT011 Huntington Disease-Like 3 38 0.032
399
CRT012 Cortical Blindness 37 0.032
400
INT020 Intravenous Leiomyomatosis 36 0.032
401
HRW001 Hair Whorl 36 0.032
402
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 35 0.032
403
c ATM022 Autoimmune Myocarditis 35 0.032
404
SLN001 Silent Myocardial Infarction 34 0.032
405
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.032
406
CND006 Candida Glabrata 32 0.032
407
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.032
408
INF021 Infant Gynecomastia 31 0.032
409
c BNG021 Benign Essential Hypertension 26 0.032
410
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.032
411
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.032
412
P CRT085 Carotid Intimal Medial Thickness 2 24 0.032
413
CGH002 Cough Headache 21 0.032
414
TLM001 Telomere Length, Mean Leukocyte 19 0.032
Content
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