Search results for Carvedilol

382 hits were found for Carvedilol

# Family MCID Name MIFTS Score
1
CNG034 Congestive Heart Failure 69 0.579
2
P HRT032 Heart Disease 75 0.483
3
c HYP595 Hypertension, Essential 84 0.452
4
c DLT002 Dilated Cardiomyopathy 79 0.353
5
c ATR087 Atrial Standstill 1 75 0.333
6
PRT013 Portal Hypertension 59 0.293
7
LVR012 Liver Cirrhosis 62 0.289
8
VRC005 Varicose Veins 60 0.269
9
c ACT075 Acute Myocardial Infarction 57 0.212
10
ANG054 Angina Pectoris 66 0.202
11
ESP002 Esophageal Varix 51 0.199
12
P ATR011 Atrial Fibrillation 66 0.196
13
ISC004 Ischemia 58 0.193
14
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.191
15
P MYC007 Myocardial Infarction 70 0.188
16
SYS003 Systolic Heart Failure 49 0.182
17
P MYC008 Myocarditis 59 0.159
18
P LVR013 Liver Disease 68 0.148
19
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.145
20
P TRN020 Turner Syndrome 67 0.145
21
LPP008 Lipoprotein Quantitative Trait Locus 62 0.145
22
P PLM037 Pulmonary Hypertension 67 0.137
23
c FML001 Familial Atrial Fibrillation 65 0.137
24
P KDN018 Kidney Disease 72 0.133
25
P CRN300 Coronary Heart Disease 1 63 0.133
26
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.128
27
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.128
28
ART140 Arteries, Anomalies of 52 0.128
29
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.124
30
ADL002 Adult Syndrome 70 0.124
31
c RHB024 Rhabdomyosarcoma 2 67 0.124
32
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.120
33
P BRS047 Breast Cancer 97 0.115
34
HYP056 Hypoglycemia 66 0.115
35
STR067 Stroke, Ischemic 81 0.110
36
CRB039 Cerebrovascular Disease 67 0.110
37
P DBT009 Diabetes Mellitus 64 0.110
38
HYP266 Hypoxia 57 0.110
39
RST023 Resting Heart Rate, Variation in 41 0.110
40
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.105
41
P VSC007 Vascular Disease 63 0.105
42
P CRD246 Cardiovascular System Disease 57 0.105
43
48X005 48,xyyy 39 0.105
44
P MSC005 Muscular Dystrophy 66 0.100
45
PRT058 Pure Autonomic Failure 59 0.100
46
CRD132 Cardiac Conduction Defect 58 0.100
47
HYP005 Hypokalemia 55 0.100
48
c MTR002 Mitral Valve Insufficiency 48 0.100
49
MSC157 Muscular Dystrophy, Duchenne Type 72 0.094
50
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.094
51
ATR057 Atrioventricular Block 55 0.094
52
INT007 Intermediate Coronary Syndrome 55 0.094
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.088
54
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.088
55
ANX010 Anxiety 73 0.088
56
c CHR684 Chronic Kidney Disease 70 0.088
57
ATH013 Atherosclerosis Susceptibility 65 0.088
58
MSC007 Muscle Hypertrophy 64 0.088
59
LPD008 Lipid Metabolism Disorder 62 0.088
60
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.088
61
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.088
62
CCN002 Cocaine Abuse 49 0.088
63
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.088
64
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.088
65
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.088
66
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.088
67
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.088
68
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.088
69
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.088
70
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.088
71
c ATM022 Autoimmune Myocarditis 35 0.088
72
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.088
73
CHL079 Children's Interstitial Lung Disease 26 0.088
74
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.081
75
P LYM118 Lymphoma 68 0.081
76
P CRD119 Cardiac Arrest 67 0.081
77
P HPT021 Hepatitis 67 0.081
78
P GLM045 Glioma 63 0.081
79
HYP066 Hyperglycemia 61 0.081
80
LNG099 Lung Disease 60 0.081
81
c HPT016 Hepatitis B 59 0.081
82
THR024 Thrombosis 57 0.081
83
LYM019 Lymphosarcoma 46 0.081
84
GLL048 Glial Tumor 45 0.081
85
P ALZ034 Alzheimer Disease 88 0.074
86
P GLM040 Glioma Susceptibility 1 81 0.074
87
GLB015 Glioblastoma Multiforme 75 0.074
88
P SLP006 Sleep Apnea 69 0.074
89
PRT036 Peritonitis 64 0.074
90
P ENC018 Encephalopathy 61 0.074
91
HPT019 Hepatic Encephalopathy 60 0.074
92
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.074
93
END086 End Stage Renal Disease 51 0.074
94
47X002 47,xyy 49 0.074
95
CCN001 Cocaine Dependence 48 0.074
96
P RNL015 Renal Hypertension 47 0.074
97
c MLG068 Malignant Glioma 46 0.074
98
MXD026 Mixed Glioma 45 0.074
99
HPT004 Hepatic Coma 45 0.074
100
DST006 Diastolic Heart Failure 45 0.074
101
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.074
102
ATX019 Ataxia with Vitamin E Deficiency 42 0.074
103
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.074
104
CYT018 Cytochrome P450 2d6 Variant 27 0.074
105
c LKM061 Leukemia, Acute Myeloid 84 0.066
106
AST005 Asthma 76 0.066
107
P RSP003 Respiratory Failure 74 0.066
108
DFC004 Deficiency Anemia 70 0.066
109
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.066
110
P LKM062 Leukemia, Acute Lymphoblastic 69 0.066
111
MSM014 Mismatch Repair Cancer Syndrome 65 0.066
112
c DBT099 Diabetes Mellitus, Type I 65 0.066
113
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.066
114
MSC152 Muscular Dystrophy, Becker Type 63 0.066
115
ALL026 Allergic Hypersensitivity Disease 62 0.066
116
FTT001 Fatty Liver Disease 61 0.066
117
P SLP005 Sleep Disorder 59 0.066
118
P ANG015 Angioedema 57 0.066
119
RSC001 Rosacea 54 0.066
120
P TRM003 Tremor 54 0.066
121
c MCR113 Microvascular Complications of Diabetes 3 52 0.066
122
ESP023 Esophageal Disease 52 0.066
123
PRT018 Portal Vein Thrombosis 50 0.066
124
RGH001 Right Bundle Branch Block 48 0.066
125
c MCR120 Microvascular Complications of Diabetes 7 47 0.066
126
ATN005 Autonomic Dysfunction 46 0.066
127
c TRC022 Tricuspid Valve Insufficiency 45 0.066
128
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.066
129
c MCR130 Microvascular Complications of Diabetes 6 41 0.066
130
c MCR133 Microvascular Complications of Diabetes 4 41 0.066
131
HYP540 Hypertension, Diastolic 40 0.066
132
HRP008 Herpes Simiae 25 0.066
133
CRR012 Cirrhotic Cardiomyopathy 24 0.066
134
P HPT023 Hepatocellular Carcinoma 100 0.057
135
MYL069 Myeloma, Multiple 85 0.057
136
P PRK057 Parkinson Disease, Late-Onset 78 0.057
137
c TBR025 Tuberous Sclerosis 1 77 0.057
138
c TBR026 Tuberous Sclerosis 2 72 0.057
139
P NRB001 Neuroblastoma 72 0.057
140
PRP027 Peripheral Vascular Disease 71 0.057
141
P EPL164 Epilepsy 71 0.057
142
DWN001 Down Syndrome 70 0.057
143
P MYP004 Myopathy 70 0.057
144
P TBR001 Tuberous Sclerosis 70 0.057
145
P LKM002 Leukemia 68 0.057
146
PSY004 Psychotic Disorder 67 0.057
147
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.057
148
OST159 Osteogenic Sarcoma 66 0.057
149
P SKN015 Skin Carcinoma 66 0.057
150
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.057
151
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.057
152
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.057
153
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.057
154
MDD011 Mood Disorder 62 0.057
155
NTR005 Nutritional Deficiency Disease 62 0.057
156
P ENC004 Encephalitis 61 0.057
157
P MYL006 Myeloid Leukemia 60 0.057
158
SPN186 Spinal Cord Injury 60 0.057
159
STT001 Status Epilepticus 60 0.057
160
c ACT071 Acute Kidney Failure 60 0.057
161
VSL002 Visual Epilepsy 59 0.057
162
ANR040 Aneurysm 59 0.057
163
c ACT073 Acute Leukemia 58 0.057
164
PST028 Post-Traumatic Stress Disorder 58 0.057
165
DSS008 Disease of Mental Health 58 0.057
166
CNS004 Constipation 58 0.057
167
IRN002 Iron Metabolism Disease 57 0.057
168
P HDC001 Headache 57 0.057
169
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.057
170
P SZR006 Seizure Disorder 56 0.057
171
AGN016 Aging 56 0.057
172
c PRG126 Progressive Familial Heart Block 55 0.057
173
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.057
174
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.057
175
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.057
176
LYM040 Lymphoblastic Lymphoma 54 0.057
177
P PNC025 Panic Disorder 53 0.057
178
P ACT105 Acute Mountain Sickness 52 0.057
179
PLS009 Plasma Cell Neoplasm 51 0.057
180
c GCH017 Gaucher Disease, Type Iii 51 0.057
181
P AST007 Astrocytoma 51 0.057
182
CRN030 Coronary Stenosis 50 0.057
183
P TMP001 Temporal Lobe Epilepsy 50 0.057
184
OPT003 Opiate Dependence 50 0.057
185
P ART018 Aortic Valve Insufficiency 49 0.057
186
LFT001 Left Bundle Branch Hemiblock 49 0.057
187
END021 Endomyocardial Fibrosis 49 0.057
188
ACT084 Acute Stress Disorder 47 0.057
189
CRD137 Cardiogenic Shock 47 0.057
190
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.057
191
c ACT076 Acute Myocarditis 46 0.057
192
OPD001 Opioid Abuse 46 0.057
193
RMS001 Rem Sleep Behavior Disorder 46 0.057
194
THR099 Third-Degree Atrioventricular Block 45 0.057
195
TRP009 Triple X Syndrome 42 0.057
196
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 0.057
197
49X006 49, Xxxxy Syndrome 41 0.057
198
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.057
199
C1N001 C1 Inhibitor Deficiency 39 0.057
200
CRN020 Coronary Restenosis 39 0.057
201
MSC012 Muscular Dystrophy, Duchenne and Becker Type 34 0.057
202
c CHR064 Chronic Monocytic Leukemia 33 0.057
203
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.057
204
SNG003 Single Ventricular Heart 30 0.057
205
P PRS040 Prostate Cancer 97 0.047
206
SCK003 Sickle Cell Anemia 74 0.047
207
c HYP836 Hypercholesterolemia, Familial, 1 73 0.047
208
MLT157 Multiple System Atrophy 1 70 0.047
209
P HYP061 Hypertrophic Cardiomyopathy 70 0.047
210
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.047
211
c HYP768 Hyperlipoproteinemia, Type I 67 0.047
212
P DMN002 Dementia 66 0.047
213
P MCR115 Microvascular Complications of Diabetes 5 66 0.047
214
CHG001 Chagas Disease 66 0.047
215
KHL003 Kohlschutter-Tonz Syndrome 65 0.047
216
P PLM036 Pulmonary Fibrosis 65 0.047
217
DMN031 Dementia, Lewy Body 65 0.047
218
PPL049 Papillon-Lefevre Syndrome 65 0.047
219
APN008 Apnea, Obstructive Sleep 64 0.047
220
P PRD008 Periodontitis 64 0.047
221
P ADN016 Adenocarcinoma 64 0.047
222
DPR016 Depression 63 0.047
223
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.047
224
SPP011 Suppression of Tumorigenicity 12 59 0.047
225
MNT002 Mental Depression 58 0.047
226
P EXN002 Exanthem 57 0.047
227
CRT033 Corticobasal Degeneration 57 0.047
228
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.047
229
P NRP001 Neuropathy 56 0.047
230
BCT022 Bacterial Infectious Disease 56 0.047
231
ACT058 Active Peptic Ulcer Disease 55 0.047
232
P SBS003 Substance Abuse 55 0.047
233
P HYP076 Hyperthyroidism 55 0.047
234
HYP060 Hyperinsulinism 54 0.047
235
TRD006 Tardive Dyskinesia 54 0.047
236
HMS001 Hemosiderosis 54 0.047
237
PRS045 Prostatic Hypertrophy 53 0.047
238
HRT012 Heart Valve Disease 53 0.047
239
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.047
240
IMP005 Impotence 52 0.047
241
END020 Endocardial Fibroelastosis 52 0.047
242
OCL069 Ocular Motor Apraxia 51 0.047
243
HYP081 Hypolipoproteinemia 51 0.047
244
HPT014 Hepatorenal Syndrome 50 0.047
245
P SCK005 Sickle Cell Disease 50 0.047
246
c INF145 Infantile Liver Failure Syndrome 1 50 0.047
247
SXL003 Sexual Disorder 47 0.047
248
STM006 Stomach Disease 47 0.047
249
CRN019 Coronary Artery Vasospasm 46 0.047
250
BNS007 Bone Sarcoma 45 0.047
251
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.047
252
ATN004 Autonomic Neuropathy 45 0.047
253
c ORT011 Orthostatic Hypotension 1 44 0.047
254
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.047
255
CYT002 Cytokine Deficiency 42 0.047
256
P RRH023 Rare Hereditary Hemochromatosis 41 0.047
257
SPR126 Superior Semicircular Canal Dehiscence 40 0.047
258
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.047
259
P DYS021 Dysautonomia 39 0.047
260
c HMG029 Hemoglobin Se Disease 39 0.047
261
c PRS136 Prostate Cancer, Hereditary, 6 33 0.047
262
c PRS130 Prostate Cancer, Hereditary, 8 32 0.047
263
CLS047 Classic Progressive Supranuclear Palsy Syndrome 31 0.047
264
FNT004 Fainting 30 0.047
265
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.047
266
DBL004 Double Discordia 23 0.047
267
KSH003 Kshv Inflammatory Cytokine Syndrome 16 0.047
268
NRL016 Neural Tube Defects 82 0.033
269
P LNG064 Lung Cancer Susceptibility 3 78 0.033
270
c BTT014 Beta-Thalassemia 74 0.033
271
SVR004 Severe Combined Immunodeficiency 73 0.033
272
ULC004 Ulcerative Colitis 73 0.033
273
c THR092 Thrombophilia Due to Thrombin Defect 73 0.033
274
P HNT016 Huntington Disease 72 0.033
275
P PHC003 Pheochromocytoma 71 0.033
276
P BRG001 Brugada Syndrome 71 0.033
277
P TTR001 Tetralogy of Fallot 70 0.033
278
P ART022 Arthritis 69 0.033
279
SVR097 Severe Cutaneous Adverse Reaction 69 0.033
280
P HYP086 Hypothyroidism 69 0.033
281
ART016 Aortic Aneurysm 69 0.033
282
P THR014 Thrombocytopenia 67 0.033
283
P LNG028 Long Qt Syndrome 66 0.033
284
P CNJ013 Conjunctivitis 65 0.033
285
PRT037 Pertussis 65 0.033
286
CLF027 Cleft Palate, Isolated 64 0.033
287
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.033
288
CLT003 Colitis 62 0.033
289
c HPT003 Hepatitis a 62 0.033
290
P HYP750 Hypertriglyceridemia, Familial 62 0.033
291
P VSC011 Vasculitis 62 0.033
292
CHL068 Cholestasis 61 0.033
293
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.033
294
DRM006 Dermatitis 61 0.033
295
c ACT027 Acute Pancreatitis 60 0.033
296
ORL011 Oral Cancer 60 0.033
297
P THL005 Thalassemia 60 0.033
298
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.033
299
P BND020 Bone Disease 59 0.033
300
IDP011 Idiopathic Interstitial Pneumonia 59 0.033
301
PLM033 Pulmonary Embolism 59 0.033
302
IRN001 Iron Deficiency Anemia 59 0.033
303
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.033
304
P BCL017 B-Cell Lymphoma 58 0.033
305
P ALC033 Alcohol Use Disorder 58 0.033
306
CNT047 Contact Dermatitis 58 0.033
307
ERY003 Erythema Multiforme 58 0.033
308
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.033
309
P PRP019 Peripheral Nervous System Disease 58 0.033
310
P GLM007 Glomerulonephritis 57 0.033
311
c MST023 Mesothelioma, Malignant 57 0.033
312
VSC002 Vascular Dementia 57 0.033
313
P BPL003 Bipolar Disorder 56 0.033
314
P MTC069 Mitochondrial Disorders 56 0.033
315
MTH009 Mouth Disease 56 0.033
316
c GRV008 Graves Disease 1 56 0.033
317
SLC006 Silicosis 56 0.033
318
P PLY019 Polyneuropathy 56 0.033
319
P ANT006 Antiphospholipid Syndrome 55 0.033
320
GLC003 Glucose Intolerance 54 0.033
321
PLM010 Pulmonary Edema 54 0.033
322
DBT010 Diabetic Neuropathy 54 0.033
323
P RTN016 Retinal Degeneration 53 0.033
324
GST023 Gastric Ulcer 53 0.033
325
PRP080 Peripheral Artery Disease 53 0.033
326
P DDN001 Duodenal Ulcer 52 0.033
327
P MSC003 Muscular Atrophy 52 0.033
328
PRS021 Prostatic Adenoma 51 0.033
329
BHR001 Behr Syndrome 51 0.033
330
CRV040 Cervix Carcinoma 51 0.033
331
PLR008 Pleurisy 50 0.033
332
c PYR010 Peyronie's Disease 50 0.033
333
c HNT004 Huntington Disease-Like 2 50 0.033
334
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.033
335
DYS073 Dysphagia 50 0.033
336
NPH010 Nephrosclerosis 50 0.033
337
HYP006 Hypertensive Heart Disease 49 0.033
338
PRS129 Prostatic Hyperplasia, Benign 49 0.033
339
HLX001 Helix Syndrome 47 0.033
340
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.033
341
c MLG069 Malignant Hypertension 47 0.033
342
RNL077 Renal Fibrosis 47 0.033
343
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.033
344
c SHR030 Short Qt Syndrome 46 0.033
345
CHD004 Chudley-Mccullough Syndrome 46 0.033
346
P BNG032 Benign Mesothelioma 46 0.033
347
ADR040 Adrenal Gland Pheochromocytoma 46 0.033
348
P MYC033 Myoclonus 46 0.033
349
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.033
350
URT010 Ureteral Obstruction 45 0.033
351
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.033
352
c CNT015 Central Sleep Apnea 45 0.033
353
CRB004 Cerebral Artery Occlusion 45 0.033
354
SBC016 Subacute Delirium 44 0.033
355
c PCH010 Pachyonychia Congenita 3 44 0.033
356
c HYP272 Hypercholesterolemia, Familial, 3 44 0.033
357
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.033
358
TST015 Testicular Disease 43 0.033
359
ALC010 Alcoholic Cardiomyopathy 42 0.033
360
c FML294 Familial Short Qt Syndrome 41 0.033
361
CNG134 Congenitally Corrected Transposition of the Great Arteries 41 0.033
362
c MJR024 Major Affective Disorder 9 41 0.033
363
ANX004 Anoxia 40 0.033
364
ANG049 Angioedema Induced by Ace Inhibitors 40 0.033
365
c HNT011 Huntington Disease-Like 3 38 0.033
366
c MJR022 Major Affective Disorder 8 38 0.033
367
P PYR039 Peyronie Disease 36 0.033
368
PSD088 Pseudobulbar Affect 36 0.033
369
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.033
370
c SHR032 Short Qt Syndrome 2 32 0.033
371
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.033
372
EXN003 Exencephaly 31 0.033
373
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.033
374
ERY066 Erythema Multiforme Major 30 0.033
375
PST092 Posttransplant Acute Limbic Encephalitis 29 0.033
376
UNV002 Univentricular Heart 28 0.033
377
c SHR031 Short Qt Syndrome 1 28 0.033
378
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.033
379
VLK001 Volkmann Contracture 25 0.033
380
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.033
381
c INF055 Infectious Myocarditis 17 0.033
382
UNC021 Unclassified Cardiomyopathy 14 0.033
Content
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