Search results for Verapamil

299 hits were found for Verapamil

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 76 0.195
2
c PYR010 Peyronie's Disease 53 0.181
3
ANG054 Angina Pectoris 66 0.170
4
ISC004 Ischemia 65 0.147
5
HDC001 Headache 59 0.142
6
P HRT032 Heart Disease 74 0.138
7
P MYC007 Myocardial Infarction 79 0.133
8
P EPL164 Epilepsy 69 0.128
9
c CNT035 Central Nervous System Disease 63 0.128
10
BRR014 Barrett Esophagus 63 0.128
11
P ENC018 Encephalopathy 62 0.128
12
P CLS010 Cluster Headache 46 0.128
13
KLD001 Keloids 49 0.123
14
P LKM002 Leukemia 72 0.118
15
P CRN018 Coronary Artery Anomaly 68 0.118
16
STR067 Stroke, Ischemic 82 0.107
17
P ATR011 Atrial Fibrillation 68 0.107
18
VSC007 Vascular Disease 68 0.107
19
P SZR006 Seizure Disorder 56 0.107
20
ISC006 Ischemic Heart Disease 72 0.101
21
CNG034 Congestive Heart Failure 72 0.101
22
ART140 Arteries, Anomalies of 65 0.101
23
c CRN300 Coronary Heart Disease 1 64 0.101
24
P NRV007 Nervous System Disease 73 0.094
25
CRB039 Cerebrovascular Disease 67 0.094
26
GLC008 Glucose Metabolism Disease 52 0.094
27
P LNG032 Lung Cancer 98 0.087
28
P DBT009 Diabetes Mellitus 64 0.087
29
GT001 Gout 57 0.087
30
CRB009 Cerebritis 41 0.087
31
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.079
32
P LYM118 Lymphoma 70 0.079
33
P SNS014 Sinusitis 62 0.079
34
RHM027 Rheumatic Disease 62 0.079
35
P ART021 Arteriosclerosis 60 0.079
36
c ACT075 Acute Myocardial Infarction 58 0.079
37
IMM136 Immune System Disease 56 0.079
38
P CLL015 Collagen Disease 52 0.079
39
PRN021 Paranasal Sinus Disease 50 0.079
40
NSD001 Nose Disease 50 0.079
41
ENT004 Enthesopathy 46 0.079
42
RVR002 Reversible Cerebral Vasoconstriction Syndrome 27 0.079
43
P BRS047 Breast Cancer 100 0.071
44
P ALZ034 Alzheimer Disease 87 0.071
45
AST005 Asthma 82 0.071
46
P DLT002 Dilated Cardiomyopathy 76 0.071
47
PSY004 Psychotic Disorder 71 0.071
48
c LKM063 Leukemia, Chronic Myeloid 70 0.071
49
P KDN018 Kidney Disease 68 0.071
50
P MYL006 Myeloid Leukemia 68 0.071
51
ATM095 Autoimmune Disease 64 0.071
52
CNN005 Connective Tissue Disease 64 0.071
53
ACQ007 Acquired Immunodeficiency Syndrome 63 0.071
54
GNG013 Gingivitis 63 0.071
55
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.071
56
WLF001 Wolff-Parkinson-White Syndrome 59 0.071
57
TYP041 Type I 56 0.071
58
P HMP006 Hemiplegic Migraine 48 0.071
59
HYP457 Hypertrophic Scars 47 0.071
60
END072 Endotheliitis 45 0.071
61
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.071
62
INS024 Insulin-Like Growth Factor I 82 0.062
63
OST012 Osteoarthritis 82 0.062
64
P PRK057 Parkinson Disease, Late-Onset 76 0.062
65
P ART022 Arthritis 76 0.062
66
P PLM037 Pulmonary Hypertension 75 0.062
67
PLY001 Polycythemia Vera 74 0.062
68
MRF001 Marfan Syndrome 74 0.062
69
BRN028 Brain Cancer 72 0.062
70
SCK003 Sickle Cell Anemia 72 0.062
71
LYM133 Lymphoma, Hodgkin, Classic 71 0.062
72
P ADN016 Adenocarcinoma 70 0.062
73
P ESS003 Essential Thrombocythemia 70 0.062
74
c SML038 Small Cell Cancer of the Lung 68 0.062
75
P ART023 Arthropathy 67 0.062
76
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.062
77
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.062
78
P LNG028 Long Qt Syndrome 65 0.062
79
HYP020 Hyperprolactinemia 63 0.062
80
RGD003 Rigid Spine Muscular Dystrophy 1 62 0.062
81
HYP056 Hypoglycemia 62 0.062
82
MRB003 Morbid Obesity 60 0.062
83
NRV006 Nervous System Cancer 60 0.062
84
ANR040 Aneurysm 60 0.062
85
ERY003 Erythema Multiforme 60 0.062
86
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 59 0.062
87
JNT002 Joint Disorders 59 0.062
88
P BPL003 Bipolar Disorder 59 0.062
89
P PLY018 Polycythemia 58 0.062
90
HMR039 Hemorrhage, Intracerebral 57 0.062
91
P CHL002 Childhood Absence Epilepsy 56 0.062
92
LYM019 Lymphosarcoma 55 0.062
93
TXC002 Toxic Encephalopathy 55 0.062
94
IMP005 Impotence 55 0.062
95
CHL061 Childhood Leukemia 55 0.062
96
CRD223 Cardiac Arrhythmia 54 0.062
97
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.062
98
THR004 Thrombocytosis 54 0.062
99
LYM024 Lymphatic System Disease 54 0.062
100
SCK005 Sickle Cell Disease 54 0.062
101
INN002 Inner Ear Disease 54 0.062
102
CLN015 Colon Adenocarcinoma 53 0.062
103
c PRM012 Primary Polycythemia 52 0.062
104
ATN002 Autonomic Nervous System Disease 51 0.062
105
DRG003 Drug Dependence 51 0.062
106
ATN005 Autonomic Dysfunction 50 0.062
107
GNG012 Gingival Overgrowth 50 0.062
108
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 48 0.062
109
CRB085 Cerebral Hemorrhage 47 0.062
110
NRR001 Neuroretinitis 46 0.062
111
SYS003 Systolic Heart Failure 46 0.062
112
PDT001 Pediatric Lymphoma 45 0.062
113
VST004 Vestibular Disease 45 0.062
114
BRN080 Brain Ischemia 44 0.062
115
SXL003 Sexual Disorder 44 0.062
116
P DYS021 Dysautonomia 43 0.062
117
P LBY004 Labyrinthitis 41 0.062
118
SCR001 Secretory Meningioma 40 0.062
119
c ADL001 Adult Lymphoma 39 0.062
120
P MYC026 Myoclonus Epilepsy 36 0.062
121
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.062
122
THR099 Third-Degree Atrioventricular Block 35 0.062
123
INT053 Intracranial Vasospasm 33 0.062
124
HDG004 Hodgkin's Granuloma 28 0.062
125
HDG006 Hodgkin's Paragranuloma 21 0.062
126
P CLR023 Colorectal Cancer 97 0.050
127
P HPT023 Hepatocellular Carcinoma 94 0.050
128
MYL069 Myeloma, Multiple 83 0.050
129
CRH001 Crohn's Disease 78 0.050
130
DPR016 Depression 72 0.050
131
SRC014 Sarcoma 68 0.050
132
DMN002 Dementia 68 0.050
133
GST050 Gastrointestinal System Disease 64 0.050
134
P LYM026 Lymphoblastic Leukemia 64 0.050
135
GST045 Gastroenteritis 64 0.050
136
P INT068 Intestinal Disease 64 0.050
137
P CRN015 Cornelia De Lange Syndrome 64 0.050
138
P THR014 Thrombocytopenia 64 0.050
139
P ESP024 Esophagitis 63 0.050
140
BND020 Bone Disease 62 0.050
141
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.050
142
CLT003 Colitis 62 0.050
143
CRD119 Cardiac Arrest 62 0.050
144
PRP030 Purpura 61 0.050
145
HYP266 Hypoxia 61 0.050
146
P HMR003 Hemorrhagic Disease 60 0.050
147
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.050
148
PLM010 Pulmonary Edema 56 0.050
149
P DRR001 Diarrhea 56 0.050
150
GLC003 Glucose Intolerance 56 0.050
151
HYP060 Hyperinsulinism 56 0.050
152
ILT001 Ileitis 56 0.050
153
URN009 Urinary System Disease 55 0.050
154
BLD053 Blood Platelet Disease 55 0.050
155
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.050
156
SPS003 Spastic Diplegia 54 0.050
157
c FML001 Familial Atrial Fibrillation 54 0.050
158
OPT003 Opiate Dependence 54 0.050
159
P GLM045 Glioma 54 0.050
160
P SCK002 Sick Sinus Syndrome 53 0.050
161
c INF071 Inflammatory Bowel Disease 1 53 0.050
162
P INF037 Inflammatory Bowel Disease 53 0.050
163
TMP001 Temporal Lobe Epilepsy 52 0.050
164
P BLD051 Blood Coagulation Disease 50 0.050
165
MCR191 Microscopic Colitis 48 0.050
166
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.050
167
URT010 Ureteral Obstruction 48 0.050
168
c CRN139 Cornelia De Lange Syndrome 1 47 0.050
169
OPD006 Opioid Addiction 45 0.050
170
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 42 0.050
171
CPL005 Capillary Disease 38 0.050
172
c SPR083 Sporadic Hemiplegic Migraine 36 0.050
173
c TRC078 Trichohepatoenteric Syndrome 2 34 0.050
174
HMC012 Hemicrania Continua 26 0.050
175
CYS001 Cystic Fibrosis 84 0.036
176
c LKM061 Leukemia, Acute Myeloid 80 0.036
177
P PNC035 Pancreatic Cancer 79 0.036
178
P HPT021 Hepatitis 76 0.036
179
P LVR013 Liver Disease 75 0.036
180
MNT001 Mantle Cell Lymphoma 73 0.036
181
PHN003 Phenylketonuria 73 0.036
182
P MYS003 Myasthenia Gravis 72 0.036
183
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.036
184
GLB002 Glioblastoma 72 0.036
185
ANX010 Anxiety 72 0.036
186
PRP027 Peripheral Vascular Disease 70 0.036
187
P ATS364 Autism 70 0.036
188
P MYL005 Myelofibrosis 70 0.036
189
P PNM007 Pneumonia 69 0.036
190
P BLD134 Bladder Cancer 69 0.036
191
WRN001 Werner Syndrome 69 0.036
192
c LKM062 Leukemia, Acute Lymphoblastic 69 0.036
193
LVR012 Liver Cirrhosis 68 0.036
194
P LPS004 Lupus Erythematosus 68 0.036
195
c THR092 Thrombophilia Due to Thrombin Defect 67 0.036
196
LNG099 Lung Disease 67 0.036
197
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.036
198
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.036
199
P HYP061 Hypertrophic Cardiomyopathy 64 0.036
200
P PNC044 Pancreatitis 64 0.036
201
GST092 Gastroesophageal Reflux 64 0.036
202
OVR029 Ovarian Hyperstimulation Syndrome 64 0.036
203
RSP006 Respiratory System Disease 63 0.036
204
PLM033 Pulmonary Embolism 62 0.036
205
MLN008 Melanoma 62 0.036
206
IRR002 Irritable Bowel Syndrome 62 0.036
207
THR024 Thrombosis 61 0.036
208
c ATS007 Autism Spectrum Disorder 61 0.036
209
INT002 Intermittent Claudication 61 0.036
210
PPT005 Peptic Ulcer Disease 61 0.036
211
P BRG001 Brugada Syndrome 60 0.036
212
CRC006 Carcinoid Syndrome 60 0.036
213
P GST044 Gastritis 60 0.036
214
GLB015 Glioblastoma Multiforme 60 0.036
215
PRS047 Prostatitis 60 0.036
216
P CTR002 Cataract 60 0.036
217
P MLG056 Malignant Hyperthermia 59 0.036
218
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.036
219
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.036
220
P PRT013 Portal Hypertension 59 0.036
221
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.036
222
SFT003 Soft Tissue Sarcoma 58 0.036
223
P EPD009 Epidermolysis Bullosa Dystrophica 58 0.036
224
P MTR012 Mitral Valve Disease 58 0.036
225
c PRG042 Progressive Familial Heart Block, Type Ia 58 0.036
226
c INT072 Intestinal Pseudo-Obstruction 57 0.036
227
c CRD093 Cardiomyopathy, Dilated, 1a 57 0.036
228
PNC034 Pancreas Disease 57 0.036
229
MNT002 Mental Depression 57 0.036
230
EPD016 Epidermolysis Bullosa 56 0.036
231
GST037 Gastroparesis 56 0.036
232
P HYP076 Hyperthyroidism 56 0.036
233
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 56 0.036
234
BNF002 Bone Fracture 55 0.036
235
NPH009 Nephrolithiasis 55 0.036
236
PRV006 Pervasive Developmental Disorder 55 0.036
237
P THY032 Thyroiditis 55 0.036
238
CLN019 Colonic Disease 54 0.036
239
PRP016 Paraplegia 53 0.036
240
PRP080 Peripheral Artery Disease 53 0.036
241
BRN071 Brain Injury 53 0.036
242
ISL001 Islet Cell Tumor 53 0.036
243
HYP005 Hypokalemia 53 0.036
244
HMG005 Hemoglobinopathy 53 0.036
245
c MCR113 Microvascular Complications of Diabetes 3 52 0.036
246
THR016 Thrombophlebitis 52 0.036
247
P GLM040 Glioma Susceptibility 1 52 0.036
248
P CTN003 Cutaneous Lupus Erythematosus 52 0.036
249
STM006 Stomach Disease 52 0.036
250
HYP080 Hypogonadism 51 0.036
251
GLL018 Gallbladder Cancer 51 0.036
252
c FML023 Familial Hemiplegic Migraine 51 0.036
253
TMT001 Timothy Syndrome 51 0.036
254
RTN023 Retinitis 50 0.036
255
HYP077 Hypertrichosis 50 0.036
256
P RNV001 Renovascular Hypertension 49 0.036
257
HPT014 Hepatorenal Syndrome 49 0.036
258
PRS045 Prostatic Hypertrophy 49 0.036
259
NPH003 Nephrocalcinosis 48 0.036
260
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.036
261
MYC005 Myocardial Stunning 47 0.036
262
AMN002 Amino Acid Metabolic Disorder 47 0.036
263
EPD070 Epidermoid Cysts 47 0.036
264
RGH001 Right Bundle Branch Block 46 0.036
265
P RNL015 Renal Hypertension 46 0.036
266
c MTR002 Mitral Valve Insufficiency 46 0.036
267
P RTN014 Retinal Artery Occlusion 46 0.036
268
CRD137 Cardiogenic Shock 45 0.036
269
HRT012 Heart Valve Disease 44 0.036
270
LYM052 Lymphomatoid Papulosis 44 0.036
271
DMP001 Dumping Syndrome 44 0.036
272
LYM067 Lymphoid Leukemia 44 0.036
273
TTR005 Tetrahydrobiopterin Deficiency 44 0.036
274
CRT015 Carotid Artery Occlusion 44 0.036
275
CLS049 Classic Phenylketonuria 42 0.036
276
HYP141 Hyperphenylalaninemia 42 0.036
277
RST023 Resting Heart Rate, Variation in 42 0.036
278
c PRG043 Progressive Familial Heart Block, Type Ib 41 0.036
279
P HYP265 Hypotonia 40 0.036
280
c MCR130 Microvascular Complications of Diabetes 6 40 0.036
281
c CNT028 Central Retinal Artery Occlusion 40 0.036
282
c MLG068 Malignant Glioma 38 0.036
283
BRD001 Brody Myopathy 38 0.036
284
ECH002 Echolalia 38 0.036
285
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.036
286
EST007 Estrogen Resistance 37 0.036
287
c MCR120 Microvascular Complications of Diabetes 7 37 0.036
288
c MCR133 Microvascular Complications of Diabetes 4 35 0.036
289
ACT118 Acute Non Lymphoblastic Leukemia 32 0.036
290
PRX009 Paroxysmal Hemicrania 32 0.036
291
DBT007 Diabetic Cataract 32 0.036
292
FNC005 Functional Colonic Disease 31 0.036
293
c MYS011 Myasthenia Gravis Congenital 30 0.036
294
CRD220 Cardiac Valvular Defect, Developmental 30 0.036
295
MLD011 Mild Hyperphenylalaninemia 30 0.036
296
AMN012 Aminoacidopathies 24 0.036
297
MLD010 Mild Phenylketonuria 24 0.036
298
ANT078 Antipyrine Metabolism 22 0.036
299
INB001 Inborn Amino Acid Metabolism Disorder 16 0.036
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