Search results for Verapamil

285 hits were found for Verapamil

# Family MCID Name MIFTS Score
1
c PYR010 Peyronie's Disease 54 0.185
2
c HYP595 Hypertension, Essential 78 0.170
3
ISC004 Ischemia 66 0.158
4
ANG054 Angina Pectoris 53 0.154
5
HDC001 Headache 55 0.145
6
P HRT032 Heart Disease 80 0.140
7
P MYC007 Myocardial Infarction 81 0.136
8
P ENC018 Encephalopathy 58 0.136
9
P EPL164 Epilepsy 70 0.131
10
c CNT035 Central Nervous System Disease 65 0.131
11
BRR014 Barrett Esophagus 64 0.131
12
P CLS010 Cluster Headache 47 0.131
13
P LKM002 Leukemia 75 0.120
14
P CRN018 Coronary Artery Anomaly 69 0.120
15
KLD001 Keloids 50 0.120
16
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.120
17
STR067 Stroke, Ischemic 84 0.109
18
P NRV007 Nervous System Disease 75 0.109
19
P ATR011 Atrial Fibrillation 68 0.109
20
P SZR006 Seizure Disorder 55 0.109
21
CNG034 Congestive Heart Failure 74 0.102
22
ISC006 Ischemic Heart Disease 73 0.102
23
VSC007 Vascular Disease 71 0.102
24
P CRN300 Coronary Heart Disease 1 57 0.102
25
ART140 Arteries, Anomalies of 51 0.102
26
CRB039 Cerebrovascular Disease 68 0.096
27
GLC008 Glucose Metabolism Disease 38 0.096
28
P RNG031 Ring Chromosome Y Syndrome 29 0.096
29
P DBT009 Diabetes Mellitus 72 0.089
30
GT001 Gout 60 0.089
31
PRN037 Prinzmetal's Variant Angina 44 0.089
32
CRB009 Cerebritis 41 0.089
33
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.081
34
c ACT075 Acute Myocardial Infarction 64 0.081
35
P ART021 Arteriosclerosis 62 0.081
36
P SNS014 Sinusitis 62 0.081
37
RHM027 Rheumatic Disease 62 0.081
38
IMM136 Immune System Disease 57 0.081
39
P CLL015 Collagen Disease 53 0.081
40
PRN021 Paranasal Sinus Disease 51 0.081
41
NSD001 Nose Disease 51 0.081
42
ENT004 Enthesopathy 38 0.081
43
RVR002 Reversible Cerebral Vasoconstriction Syndrome 27 0.081
44
P BRS047 Breast Cancer 100 0.072
45
P ALZ034 Alzheimer Disease 95 0.072
46
AST005 Asthma 83 0.072
47
P DLT002 Dilated Cardiomyopathy 76 0.072
48
PSY004 Psychotic Disorder 72 0.072
49
P LYM118 Lymphoma 71 0.072
50
P KDN018 Kidney Disease 69 0.072
51
P MYL006 Myeloid Leukemia 69 0.072
52
ATM095 Autoimmune Disease 66 0.072
53
ACQ007 Acquired Immunodeficiency Syndrome 65 0.072
54
CNN005 Connective Tissue Disease 65 0.072
55
GNG013 Gingivitis 64 0.072
56
MGR028 Migraine with or Without Aura 1 55 0.072
57
P HMP006 Hemiplegic Migraine 49 0.072
58
END072 Endotheliitis 46 0.072
59
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.072
60
P LNG032 Lung Cancer 99 0.063
61
OST012 Osteoarthritis 88 0.063
62
INS024 Insulin-Like Growth Factor I 83 0.063
63
c LKM063 Leukemia, Chronic Myeloid 80 0.063
64
LYM133 Lymphoma, Hodgkin, Classic 78 0.063
65
P PRK057 Parkinson Disease, Late-Onset 78 0.063
66
P ART022 Arthritis 77 0.063
67
PLY001 Polycythemia Vera 75 0.063
68
MRF001 Marfan Syndrome 75 0.063
69
SCK003 Sickle Cell Anemia 73 0.063
70
BRN028 Brain Cancer 72 0.063
71
P ADN016 Adenocarcinoma 71 0.063
72
P ESS003 Essential Thrombocythemia 71 0.063
73
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.063
74
P ART023 Arthropathy 68 0.063
75
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.063
76
HYP020 Hyperprolactinemia 64 0.063
77
P LNG028 Long Qt Syndrome 63 0.063
78
HYP056 Hypoglycemia 62 0.063
79
NRV006 Nervous System Cancer 61 0.063
80
MRB003 Morbid Obesity 61 0.063
81
ANR040 Aneurysm 61 0.063
82
P BPL003 Bipolar Disorder 61 0.063
83
JNT002 Joint Disorders 60 0.063
84
P PLY018 Polycythemia 60 0.063
85
ERY003 Erythema Multiforme 60 0.063
86
RGD003 Rigid Spine Muscular Dystrophy 1 59 0.063
87
LYM019 Lymphosarcoma 58 0.063
88
WLF001 Wolff-Parkinson-White Syndrome 57 0.063
89
P CHL002 Childhood Absence Epilepsy 56 0.063
90
THR004 Thrombocytosis 55 0.063
91
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.063
92
TXC002 Toxic Encephalopathy 55 0.063
93
SCK005 Sickle Cell Disease 54 0.063
94
IMP005 Impotence 54 0.063
95
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.063
96
CLN015 Colon Adenocarcinoma 53 0.063
97
c PRM012 Primary Polycythemia 53 0.063
98
INN002 Inner Ear Disease 52 0.063
99
GNG012 Gingival Overgrowth 52 0.063
100
ATN002 Autonomic Nervous System Disease 51 0.063
101
ATN005 Autonomic Dysfunction 51 0.063
102
DRG003 Drug Dependence 51 0.063
103
HYP457 Hypertrophic Scars 48 0.063
104
P DYS021 Dysautonomia 47 0.063
105
NRR001 Neuroretinitis 46 0.063
106
VST004 Vestibular Disease 45 0.063
107
SXL003 Sexual Disorder 45 0.063
108
LYM024 Lymphatic System Disease 45 0.063
109
BRN080 Brain Ischemia 45 0.063
110
SYS003 Systolic Heart Failure 44 0.063
111
P LBY004 Labyrinthitis 41 0.063
112
SCR001 Secretory Meningioma 41 0.063
113
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 41 0.063
114
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.063
115
P MYC026 Myoclonus Epilepsy 35 0.063
116
HDG004 Hodgkin's Granuloma 28 0.063
117
INT053 Intracranial Vasospasm 25 0.063
118
HDG006 Hodgkin's Paragranuloma 21 0.063
119
CRH001 Crohn's Disease 80 0.051
120
ANX010 Anxiety 72 0.051
121
DMN002 Dementia 68 0.051
122
P LYM026 Lymphoblastic Leukemia 66 0.051
123
GST050 Gastrointestinal System Disease 66 0.051
124
P CRN015 Cornelia De Lange Syndrome 65 0.051
125
GST045 Gastroenteritis 65 0.051
126
P INT068 Intestinal Disease 65 0.051
127
P THR014 Thrombocytopenia 65 0.051
128
P ESP024 Esophagitis 64 0.051
129
CLT003 Colitis 63 0.051
130
PRP030 Purpura 61 0.051
131
HYP266 Hypoxia 61 0.051
132
P HMR003 Hemorrhagic Disease 61 0.051
133
P GLM045 Glioma 61 0.051
134
P DRR001 Diarrhea 60 0.051
135
URN009 Urinary System Disease 58 0.051
136
GLC003 Glucose Intolerance 58 0.051
137
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.051
138
HYP060 Hyperinsulinism 56 0.051
139
SPS003 Spastic Diplegia 55 0.051
140
c FML001 Familial Atrial Fibrillation 55 0.051
141
c INF071 Inflammatory Bowel Disease 1 54 0.051
142
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.051
143
OPT003 Opiate Dependence 54 0.051
144
TMP001 Temporal Lobe Epilepsy 54 0.051
145
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.051
146
P SCK002 Sick Sinus Syndrome 53 0.051
147
CRD223 Cardiac Arrhythmia 52 0.051
148
ILT001 Ileitis 52 0.051
149
P INF037 Inflammatory Bowel Disease 52 0.051
150
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.051
151
MCR191 Microscopic Colitis 50 0.051
152
URT010 Ureteral Obstruction 49 0.051
153
c CRN139 Cornelia De Lange Syndrome 1 46 0.051
154
BLD053 Blood Platelet Disease 45 0.051
155
OPD006 Opioid Addiction 43 0.051
156
CPL005 Capillary Disease 38 0.051
157
P BLD051 Blood Coagulation Disease 38 0.051
158
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.051
159
c SPR083 Sporadic Hemiplegic Migraine 33 0.051
160
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.051
161
HMC012 Hemicrania Continua 26 0.051
162
P CLR023 Colorectal Cancer 98 0.036
163
P HPT023 Hepatocellular Carcinoma 94 0.036
164
P PNC035 Pancreatic Cancer 89 0.036
165
MYL069 Myeloma, Multiple 86 0.036
166
CYS001 Cystic Fibrosis 85 0.036
167
c LKM061 Leukemia, Acute Myeloid 81 0.036
168
P PLM037 Pulmonary Hypertension 79 0.036
169
P LVR013 Liver Disease 76 0.036
170
MNT001 Mantle Cell Lymphoma 76 0.036
171
P MYL005 Myelofibrosis 75 0.036
172
P HPT021 Hepatitis 75 0.036
173
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.036
174
GLB002 Glioblastoma 74 0.036
175
PHN003 Phenylketonuria 73 0.036
176
P MYS003 Myasthenia Gravis 73 0.036
177
LVR012 Liver Cirrhosis 73 0.036
178
MLN008 Melanoma 72 0.036
179
PRP027 Peripheral Vascular Disease 71 0.036
180
P PNM007 Pneumonia 70 0.036
181
WRN001 Werner Syndrome 70 0.036
182
P ATS364 Autism 70 0.036
183
P LPS004 Lupus Erythematosus 69 0.036
184
GLB015 Glioblastoma Multiforme 68 0.036
185
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.036
186
c ATS007 Autism Spectrum Disorder 68 0.036
187
SRC014 Sarcoma 68 0.036
188
GLL018 Gallbladder Cancer 67 0.036
189
LNG099 Lung Disease 67 0.036
190
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.036
191
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.036
192
c SML038 Small Cell Cancer of the Lung 67 0.036
193
c MLG068 Malignant Glioma 66 0.036
194
P HYP061 Hypertrophic Cardiomyopathy 65 0.036
195
OVR029 Ovarian Hyperstimulation Syndrome 64 0.036
196
GST092 Gastroesophageal Reflux 64 0.036
197
P PNC044 Pancreatitis 64 0.036
198
RSP006 Respiratory System Disease 63 0.036
199
CRD119 Cardiac Arrest 63 0.036
200
IRR002 Irritable Bowel Syndrome 63 0.036
201
PLM033 Pulmonary Embolism 62 0.036
202
THR024 Thrombosis 61 0.036
203
INT002 Intermittent Claudication 61 0.036
204
P BRG001 Brugada Syndrome 61 0.036
205
c THR092 Thrombophilia Due to Thrombin Defect 61 0.036
206
P GST044 Gastritis 61 0.036
207
P CTR002 Cataract 60 0.036
208
MNT002 Mental Depression 60 0.036
209
P PRT013 Portal Hypertension 59 0.036
210
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.036
211
PRS047 Prostatitis 59 0.036
212
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.036
213
P EPD009 Epidermolysis Bullosa Dystrophica 59 0.036
214
P MTR012 Mitral Valve Disease 59 0.036
215
ALL026 Allergic Hypersensitivity Disease 59 0.036
216
PNC034 Pancreas Disease 59 0.036
217
CRC006 Carcinoid Syndrome 59 0.036
218
SFT003 Soft Tissue Sarcoma 58 0.036
219
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.036
220
c INT072 Intestinal Pseudo-Obstruction 57 0.036
221
EPD016 Epidermolysis Bullosa 57 0.036
222
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.036
223
NPH009 Nephrolithiasis 57 0.036
224
P THY032 Thyroiditis 56 0.036
225
GST037 Gastroparesis 56 0.036
226
PRV006 Pervasive Developmental Disorder 56 0.036
227
CLN019 Colonic Disease 55 0.036
228
c MCR113 Microvascular Complications of Diabetes 3 55 0.036
229
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.036
230
ISL001 Islet Cell Tumor 54 0.036
231
PRP080 Peripheral Artery Disease 54 0.036
232
HYP080 Hypogonadism 54 0.036
233
HYP005 Hypokalemia 53 0.036
234
P CTN003 Cutaneous Lupus Erythematosus 53 0.036
235
HMG005 Hemoglobinopathy 53 0.036
236
PRP016 Paraplegia 53 0.036
237
THR016 Thrombophlebitis 53 0.036
238
STM006 Stomach Disease 52 0.036
239
RTN023 Retinitis 52 0.036
240
TMT001 Timothy Syndrome 52 0.036
241
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.036
242
P GLM040 Glioma Susceptibility 1 51 0.036
243
c FML023 Familial Hemiplegic Migraine 51 0.036
244
PRS045 Prostatic Hypertrophy 51 0.036
245
HPT014 Hepatorenal Syndrome 49 0.036
246
NPH003 Nephrocalcinosis 49 0.036
247
HYP077 Hypertrichosis 49 0.036
248
P RNV001 Renovascular Hypertension 48 0.036
249
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.036
250
MYC005 Myocardial Stunning 47 0.036
251
P RNL015 Renal Hypertension 46 0.036
252
EPD070 Epidermoid Cysts 46 0.036
253
c MTR002 Mitral Valve Insufficiency 46 0.036
254
P RTN014 Retinal Artery Occlusion 45 0.036
255
CRD137 Cardiogenic Shock 45 0.036
256
LYM052 Lymphomatoid Papulosis 45 0.036
257
DMP001 Dumping Syndrome 45 0.036
258
RGH001 Right Bundle Branch Block 44 0.036
259
TTR005 Tetrahydrobiopterin Deficiency 44 0.036
260
LYM067 Lymphoid Leukemia 43 0.036
261
CLS049 Classic Phenylketonuria 43 0.036
262
HYP141 Hyperphenylalaninemia 43 0.036
263
CRT015 Carotid Artery Occlusion 42 0.036
264
RST023 Resting Heart Rate, Variation in 42 0.036
265
c MCR130 Microvascular Complications of Diabetes 6 42 0.036
266
BRD001 Brody Myopathy 41 0.036
267
EST007 Estrogen Resistance 40 0.036
268
P HYP265 Hypotonia 40 0.036
269
c PRG043 Progressive Familial Heart Block, Type Ib 40 0.036
270
c CNT028 Central Retinal Artery Occlusion 40 0.036
271
AMN002 Amino Acid Metabolic Disorder 38 0.036
272
DBT007 Diabetic Cataract 38 0.036
273
c BLD140 Blood Group, I System 37 0.036
274
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.036
275
MNG003 Mungan Syndrome 34 0.036
276
c MCR120 Microvascular Complications of Diabetes 7 34 0.036
277
c TRC078 Trichohepatoenteric Syndrome 2 34 0.036
278
ACT118 Acute Non Lymphoblastic Leukemia 32 0.036
279
c MCR133 Microvascular Complications of Diabetes 4 32 0.036
280
c MYS011 Myasthenia Gravis Congenital 28 0.036
281
PRX009 Paroxysmal Hemicrania 25 0.036
282
FNC005 Functional Colonic Disease 24 0.036
283
ANT078 Antipyrine Metabolism 22 0.036
284
INB001 Inborn Amino Acid Metabolism Disorder 16 0.036
285
AMN012 Aminoacidopathies 15 0.036
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