Search results for Verapamil

648 hits were found for Verapamil

# Family MCID Name MIFTS Score
1
ANG054 Angina Pectoris 66 0.365
2
c HYP595 Hypertension, Essential 87 0.334
3
P ATR011 Atrial Fibrillation 67 0.292
4
c ATR087 Atrial Standstill 1 76 0.282
5
P HYP061 Hypertrophic Cardiomyopathy 68 0.266
6
c ACT075 Acute Myocardial Infarction 59 0.265
7
ATR057 Atrioventricular Block 56 0.246
8
P MYC007 Myocardial Infarction 74 0.218
9
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.211
10
ISC004 Ischemia 62 0.206
11
CNG034 Congestive Heart Failure 69 0.183
12
P CRN018 Coronary Artery Anomaly 67 0.183
13
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.179
14
CNS004 Constipation 59 0.179
15
ART140 Arteries, Anomalies of 60 0.175
16
P HDC001 Headache 59 0.169
17
P KDN018 Kidney Disease 73 0.164
18
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.162
19
INT007 Intermediate Coronary Syndrome 58 0.162
20
P CRD119 Cardiac Arrest 71 0.160
21
c PYR010 Peyronie's Disease 51 0.160
22
c MGR028 Migraine with or Without Aura 1 70 0.153
23
P HRT032 Heart Disease 78 0.145
24
WLF001 Wolff-Parkinson-White Syndrome 65 0.145
25
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.143
26
RGH001 Right Bundle Branch Block 48 0.143
27
P CLS010 Cluster Headache 44 0.143
28
P PLM037 Pulmonary Hypertension 69 0.140
29
CRD137 Cardiogenic Shock 50 0.138
30
IMP005 Impotence 53 0.127
31
HYP266 Hypoxia 58 0.121
32
48X005 48,xyyy 37 0.121
33
LVR012 Liver Cirrhosis 67 0.118
34
c ACT071 Acute Kidney Failure 60 0.118
35
P SZR006 Seizure Disorder 59 0.118
36
KLD004 Keloid Disorder 41 0.118
37
RST023 Resting Heart Rate, Variation in 43 0.115
38
c DLT002 Dilated Cardiomyopathy 81 0.111
39
VSL002 Visual Epilepsy 58 0.111
40
STR067 Stroke, Ischemic 82 0.108
41
P BLD134 Bladder Cancer 79 0.108
42
CRB039 Cerebrovascular Disease 71 0.108
43
HYP056 Hypoglycemia 68 0.108
44
DPR016 Depression 64 0.108
45
CRD223 Cardiac Arrhythmia 61 0.108
46
P PYR039 Peyronie Disease 41 0.108
47
P EPL164 Epilepsy 73 0.105
48
ATH013 Atherosclerosis Susceptibility 68 0.105
49
P TRN020 Turner Syndrome 66 0.105
50
ALL026 Allergic Hypersensitivity Disease 65 0.105
51
P CRN300 Coronary Heart Disease 1 59 0.105
52
SYN036 Syncope 46 0.105
53
HYP066 Hyperglycemia 63 0.101
54
ATR089 Atrioventricular Dissociation 20 0.097
55
P LNG028 Long Qt Syndrome 68 0.094
56
PRT013 Portal Hypertension 61 0.094
57
P LYM031 Lymphocytic Leukemia 56 0.094
58
HYP457 Hypertrophic Scars 44 0.094
59
CLN015 Colon Adenocarcinoma 65 0.090
60
HYP020 Hyperprolactinemia 62 0.090
61
MTB004 Metabolic Acidosis 48 0.090
62
SCN049 Second-Degree Atrioventricular Block 27 0.090
63
P OVR042 Ovarian Cancer 89 0.085
64
MYL069 Myeloma, Multiple 85 0.085
65
P SCH015 Schizophrenia 76 0.085
66
c FML001 Familial Atrial Fibrillation 67 0.085
67
P VSC007 Vascular Disease 65 0.085
68
STT001 Status Epilepticus 61 0.085
69
P SCK002 Sick Sinus Syndrome 56 0.085
70
HYP005 Hypokalemia 55 0.085
71
PNG002 Pain Agnosia 52 0.085
72
AST005 Asthma 80 0.081
73
P LKM002 Leukemia 69 0.081
74
P DBT009 Diabetes Mellitus 66 0.081
75
P HYP069 Hyperparathyroidism 64 0.081
76
LNG099 Lung Disease 62 0.081
77
PLM010 Pulmonary Edema 56 0.081
78
CRN019 Coronary Artery Vasospasm 48 0.081
79
LFT001 Left Bundle Branch Hemiblock 47 0.081
80
P CLR023 Colorectal Cancer 100 0.076
81
P MSC005 Muscular Dystrophy 68 0.076
82
c SML038 Small Cell Cancer of the Lung 67 0.076
83
P GLM045 Glioma 64 0.076
84
P MYC008 Myocarditis 60 0.076
85
CMR002 Coumarin Resistance 56 0.076
86
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.076
87
P DDN001 Duodenal Ulcer 50 0.076
88
GLL048 Glial Tumor 48 0.076
89
CYT002 Cytokine Deficiency 46 0.076
90
P LNG032 Lung Cancer 99 0.071
91
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.071
92
P RSP003 Respiratory Failure 75 0.071
93
GLB002 Glioblastoma 74 0.071
94
c CHR684 Chronic Kidney Disease 68 0.071
95
P ADN016 Adenocarcinoma 65 0.071
96
P CTR002 Cataract 62 0.071
97
GLB015 Glioblastoma Multiforme 60 0.071
98
c ACT027 Acute Pancreatitis 60 0.071
99
P BPL003 Bipolar Disorder 59 0.071
100
c ACT210 Acute Respiratory Distress Syndrome 59 0.071
101
P EXN002 Exanthem 58 0.071
102
AGN016 Aging 58 0.071
103
c MCR113 Microvascular Complications of Diabetes 3 55 0.071
104
HYP060 Hyperinsulinism 55 0.071
105
c MCR120 Microvascular Complications of Diabetes 7 48 0.071
106
BHR001 Behr Syndrome 47 0.071
107
P RNL015 Renal Hypertension 47 0.071
108
ATX019 Ataxia with Vitamin E Deficiency 46 0.071
109
ANX004 Anoxia 44 0.071
110
c MCR130 Microvascular Complications of Diabetes 6 42 0.071
111
c MCR133 Microvascular Complications of Diabetes 4 42 0.071
112
THR099 Third-Degree Atrioventricular Block 39 0.071
113
MLT131 Multifocal Atrial Tachycardia 19 0.071
114
P HPT023 Hepatocellular Carcinoma 99 0.066
115
P BRS047 Breast Cancer 99 0.066
116
c HYP836 Hypercholesterolemia, Familial, 1 74 0.066
117
PRP027 Peripheral Vascular Disease 72 0.066
118
P HYP086 Hypothyroidism 70 0.066
119
P LKM062 Leukemia, Acute Lymphoblastic 68 0.066
120
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 68 0.066
121
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.066
122
P NRB010 Neuroblastoma 1 66 0.066
123
P NTR004 Neutropenia 64 0.066
124
P MYL006 Myeloid Leukemia 61 0.066
125
PRT058 Pure Autonomic Failure 60 0.066
126
TRD006 Tardive Dyskinesia 58 0.066
127
P NRP001 Neuropathy 57 0.066
128
P HYP076 Hyperthyroidism 55 0.066
129
P DRR001 Diarrhea 55 0.066
130
GLC003 Glucose Intolerance 55 0.066
131
OVR082 Overgrowth Syndrome 51 0.066
132
RYN005 Raynaud Phenomenon 50 0.066
133
c MJR024 Major Affective Disorder 9 42 0.066
134
HYP540 Hypertension, Diastolic 41 0.066
135
c MJR022 Major Affective Disorder 8 39 0.066
136
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.066
137
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.060
138
c LKM071 Leukemia, Chronic Lymphocytic 81 0.060
139
OST012 Osteoarthritis 80 0.060
140
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.060
141
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.060
142
c MNN043 Meningioma, Familial 74 0.060
143
P MCR115 Microvascular Complications of Diabetes 5 67 0.060
144
OST159 Osteogenic Sarcoma 67 0.060
145
CHG001 Chagas Disease 66 0.060
146
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.060
147
MNN042 Meningioma, Radiation-Induced 64 0.060
148
LPD008 Lipid Metabolism Disorder 64 0.060
149
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.060
150
CLT003 Colitis 63 0.060
151
ADL002 Adult Syndrome 62 0.060
152
TTN003 Tetanus 62 0.060
153
TRN015 Transient Cerebral Ischemia 62 0.060
154
PPT005 Peptic Ulcer Disease 60 0.060
155
INT002 Intermittent Claudication 60 0.060
156
ERL001 Early Myoclonic Encephalopathy 60 0.060
157
END030 End Stage Renal Failure 60 0.060
158
CMM005 Common Cold 57 0.060
159
ERY003 Erythema Multiforme 57 0.060
160
P ART021 Arteriosclerosis 56 0.060
161
P MTR003 Mitral Valve Stenosis 54 0.060
162
P TMP001 Temporal Lobe Epilepsy 53 0.060
163
GNG012 Gingival Overgrowth 52 0.060
164
STM007 Stomatitis 51 0.060
165
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.060
166
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.060
167
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.060
168
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.060
169
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.060
170
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.060
171
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.060
172
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.060
173
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.060
174
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.060
175
P HMP006 Hemiplegic Migraine 45 0.060
176
ACT003 Acute Kidney Tubular Necrosis 42 0.060
177
SPN021 Spinal Meningioma 40 0.060
178
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.060
179
SCR001 Secretory Meningioma 38 0.060
180
c LKM004 Leukemia, B-Cell, Chronic 35 0.060
181
RVR002 Reversible Cerebral Vasoconstriction Syndrome 29 0.060
182
P PNC035 Pancreatic Cancer 86 0.054
183
c LKM061 Leukemia, Acute Myeloid 84 0.054
184
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.054
185
P MDL005 Medulloblastoma 78 0.054
186
DFC004 Deficiency Anemia 77 0.054
187
MRF001 Marfan Syndrome 75 0.054
188
CRH001 Crohn's Disease 75 0.054
189
c LKM063 Leukemia, Chronic Myeloid 74 0.054
190
MSC157 Muscular Dystrophy, Duchenne Type 70 0.054
191
DWN001 Down Syndrome 70 0.054
192
P MYS003 Myasthenia Gravis 68 0.054
193
P ORT004 Orthostatic Intolerance 68 0.054
194
c MCR129 Microvascular Complications of Diabetes 1 67 0.054
195
IRR002 Irritable Bowel Syndrome 65 0.054
196
P CRD132 Cardiac Conduction Defect 61 0.054
197
INS001 Insulinoma 60 0.054
198
P MLG056 Malignant Hyperthermia 60 0.054
199
c ACT073 Acute Leukemia 59 0.054
200
P ALP008 Alopecia 58 0.054
201
FCL014 Focal Epilepsy 56 0.054
202
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.054
203
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.054
204
STT041 Stuttering 53 0.054
205
c SCN007 Secondary Hyperparathyroidism 52 0.054
206
BNR002 Bone Resorption Disease 51 0.054
207
URM002 Uremia 50 0.054
208
CRN030 Coronary Stenosis 49 0.054
209
TST044 Testicular Torsion 49 0.054
210
47X002 47,xyy 49 0.054
211
WTH001 Withdrawal Disorder 47 0.054
212
URT010 Ureteral Obstruction 46 0.054
213
SNT005 Sinoatrial Node Disease 46 0.054
214
HLX001 Helix Syndrome 46 0.054
215
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.054
216
P MJR007 Major Affective Disorder 1 44 0.054
217
c MCR112 Microvascular Complications of Diabetes 2 42 0.054
218
CLC008 Colchicine Resistance 38 0.054
219
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 37 0.054
220
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.054
221
INT053 Intracranial Vasospasm 32 0.054
222
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.054
223
P GST053 Gastric Cancer 85 0.047
224
P RTT002 Rett Syndrome 81 0.047
225
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.047
226
BRN028 Brain Cancer 75 0.047
227
ANX010 Anxiety 75 0.047
228
SCK003 Sickle Cell Anemia 74 0.047
229
LPT014 Leptin Deficiency or Dysfunction 72 0.047
230
P PHC003 Pheochromocytoma 71 0.047
231
P LVR013 Liver Disease 71 0.047
232
P BRG001 Brugada Syndrome 70 0.047
233
PLY001 Polycythemia Vera 70 0.047
234
LYM133 Lymphoma, Hodgkin, Classic 70 0.047
235
P ESS003 Essential Thrombocythemia 69 0.047
236
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.047
237
THY111 Thyroid Carcinoma, Familial Medullary 68 0.047
238
PRT037 Pertussis 66 0.047
239
SVR097 Severe Cutaneous Adverse Reaction 66 0.047
240
c INF071 Inflammatory Bowel Disease 1 66 0.047
241
P DYS154 Dystonia 65 0.047
242
P VSC011 Vasculitis 64 0.047
243
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.047
244
P ENC018 Encephalopathy 64 0.047
245
c PRC016 Pre-Eclampsia 63 0.047
246
TXC005 Toxic Shock Syndrome 63 0.047
247
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.047
248
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.047
249
THY029 Thyroid Carcinoma 62 0.047
250
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.047
251
P ADL010 Adult Respiratory Distress Syndrome 61 0.047
252
GNG013 Gingivitis 60 0.047
253
c PRM005 Primary Hyperparathyroidism 60 0.047
254
HMR039 Hemorrhage, Intracerebral 59 0.047
255
ERY051 Erythroleukemia, Familial 58 0.047
256
CRH005 Crohn's Colitis 56 0.047
257
P PLY018 Polycythemia 56 0.047
258
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.047
259
LNN001 Lennox-Gastaut Syndrome 56 0.047
260
CRC006 Carcinoid Syndrome 55 0.047
261
c GRV008 Graves Disease 1 55 0.047
262
HMP005 Hemiplegia 55 0.047
263
TXC002 Toxic Encephalopathy 54 0.047
264
c FML023 Familial Hemiplegic Migraine 54 0.047
265
c FML191 Familial Long Qt Syndrome 54 0.047
266
OCL069 Ocular Motor Apraxia 53 0.047
267
P SCK005 Sickle Cell Disease 53 0.047
268
P MRD002 Marden-Walker Syndrome 53 0.047
269
OCL006 Ocular Hypertension 52 0.047
270
THY125 Thyroid Gland Medullary Carcinoma 52 0.047
271
c PRM012 Primary Polycythemia 52 0.047
272
ADR040 Adrenal Gland Pheochromocytoma 51 0.047
273
c SVR005 Severe Pre-Eclampsia 50 0.047
274
P OPN001 Open-Angle Glaucoma 50 0.047
275
HYD012 Hydrops Fetalis 49 0.047
276
c MTR002 Mitral Valve Insufficiency 49 0.047
277
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.047
278
c CNG389 Congenital Disorder of Glycosylation, Type Iim 48 0.047
279
PRM020 Premenstrual Tension 48 0.047
280
ATN005 Autonomic Dysfunction 48 0.047
281
DRG003 Drug Dependence 48 0.047
282
c THR090 Thrombocythemia 1 47 0.047
283
P CMP008 Compartment Syndrome 45 0.047
284
PRL017 Prolymphocytic Leukemia 45 0.047
285
MYC005 Myocardial Stunning 45 0.047
286
DMP001 Dumping Syndrome 44 0.047
287
DRG024 Drug Allergy 43 0.047
288
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.047
289
SYS003 Systolic Heart Failure 43 0.047
290
RDN001 Reading Disorder 42 0.047
291
P DYS021 Dysautonomia 41 0.047
292
FRS012 First-Degree Atrioventricular Block 39 0.047
293
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 39 0.047
294
CRB004 Cerebral Artery Occlusion 38 0.047
295
P INT260 Intracranial Berry Aneurysm 38 0.047
296
CNT017 Central Nervous System Origin Vertigo 38 0.047
297
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.047
298
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 36 0.047
299
c MJR008 Major Affective Disorder 2 35 0.047
300
P MYC026 Myoclonus Epilepsy 34 0.047
301
c MJR003 Major Affective Disorder 6 34 0.047
302
c MJR006 Major Affective Disorder 5 34 0.047
303
c MJR023 Major Affective Disorder 7 34 0.047
304
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.047
305
c MJR004 Major Affective Disorder 4 29 0.047
306
ERY066 Erythema Multiforme Major 29 0.047
307
CYT018 Cytochrome P450 2d6 Variant 28 0.047
308
c PRC045 Preeclampsia/eclampsia 5 25 0.047
309
FTL016 Fetal Edema 24 0.047
310
c PRC034 Preeclampsia/eclampsia 4 24 0.047
311
P ALZ034 Alzheimer Disease 90 0.038
312
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.038
313
P RHM011 Rheumatoid Arthritis 82 0.038
314
P MLT020 Multiple Sclerosis 73 0.038
315
P SRC025 Sarcoidosis 1 72 0.038
316
ADN011 Adenoid Cystic Carcinoma 71 0.038
317
ART016 Aortic Aneurysm 71 0.038
318
P LYM118 Lymphoma 70 0.038
319
MNT001 Mantle Cell Lymphoma 69 0.038
320
P HPT021 Hepatitis 69 0.038
321
ALL003 Allergic Rhinitis 69 0.038
322
PNC129 Pancreatic Adenocarcinoma 69 0.038
323
MLN008 Melanoma 68 0.038
324
GST040 Gastric Adenocarcinoma 67 0.038
325
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.038
326
P PRS038 Personality Disorder 66 0.038
327
P HRP006 Herpes Simplex 66 0.038
328
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.038
329
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.038
330
c RHB024 Rhabdomyosarcoma 2 64 0.038
331
LSH001 Leishmaniasis 64 0.038
332
P MVM001 Movement Disease 63 0.038
333
P END044 Endometriosis 63 0.038
334
P HYP750 Hypertriglyceridemia, Familial 62 0.038
335
VRL011 Viral Infectious Disease 62 0.038
336
CRC021 Carcinosarcoma 62 0.038
337
c SCL052 Scleroderma, Familial Progressive 62 0.038
338
ATM095 Autoimmune Disease 62 0.038
339
P PNC044 Pancreatitis 61 0.038
340
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.038
341
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.038
342
MNT002 Mental Depression 60 0.038
343
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.038
344
THR024 Thrombosis 58 0.038
345
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.038
346
P FBR017 Fibrosarcoma 57 0.038
347
TRN018 Transitional Cell Carcinoma 57 0.038
348
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.038
349
PRP030 Purpura 56 0.038
350
MCS002 Mucositis 56 0.038
351
P LTR001 Lateral Sclerosis 56 0.038
352
P SBS003 Substance Abuse 56 0.038
353
P TRM003 Tremor 55 0.038
354
PRS045 Prostatic Hypertrophy 55 0.038
355
BRD001 Brody Myopathy 55 0.038
356
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.038
357
INT075 Intracranial Hypertension 54 0.038
358
P DBT005 Diabetes Insipidus 54 0.038
359
HMS001 Hemosiderosis 54 0.038
360
RSP002 Respiratory Syncytial Virus Infectious Disease 54 0.038
361
P ECL001 Eclampsia 53 0.038
362
P MYM013 Moyamoya Disease 1 53 0.038
363
GST023 Gastric Ulcer 53 0.038
364
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 52 0.038
365
NPH003 Nephrocalcinosis 52 0.038
366
PRP080 Peripheral Artery Disease 51 0.038
367
OPT003 Opiate Dependence 50 0.038
368
ACH005 Achalasia 50 0.038
369
SXL003 Sexual Disorder 49 0.038
370
OPD006 Opioid Addiction 49 0.038
371
TST014 Testicular Cancer 49 0.038
372
ATS010 Autosomal Recessive Disease 49 0.038
373
HPT014 Hepatorenal Syndrome 49 0.038
374
LYM019 Lymphosarcoma 48 0.038
375
P PRD021 Periodic Paralysis 47 0.038
376
PTT037 Pituitary Tumors 47 0.038
377
MCR191 Microscopic Colitis 47 0.038
378
MLT006 Multidrug-Resistant Tuberculosis 46 0.038
379
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.038
380
GLC096 Galactorrhea 44 0.038
381
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.038
382
PLY068 Polysubstance Abuse 44 0.038
383
CRT015 Carotid Artery Occlusion 44 0.038
384
P KLZ004 Kala-Azar 1 43 0.038
385
DBT007 Diabetic Cataract 42 0.038
386
ANG049 Angioedema Induced by Ace Inhibitors 41 0.038
387
CRB086 Cerebral Aneurysms 41 0.038
388
P RRH023 Rare Hereditary Hemochromatosis 41 0.038
389
OVR094 Ovarian Epithelial Cancer 39 0.038
390
c HNT011 Huntington Disease-Like 3 37 0.038
391
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 37 0.038
392
c SPR083 Sporadic Hemiplegic Migraine 30 0.038
393
HMC012 Hemicrania Continua 29 0.038
394
ACT118 Acute Non Lymphoblastic Leukemia 27 0.038
395
KDN013 Kidney Hypertrophy 27 0.038
396
HDG004 Hodgkin's Granuloma 27 0.038
397
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.038
398
HDG006 Hodgkin's Paragranuloma 23 0.038
399
BDR001 Bidirectional Tachycardia 19 0.038
400
P PRS040 Prostate Cancer 97 0.027
401
CYS001 Cystic Fibrosis 84 0.027
402
MLR004 Malaria 82 0.027
403
IMM167 Immune Deficiency Disease 79 0.027
404
CRV035 Cervical Cancer 77 0.027
405
ULC004 Ulcerative Colitis 75 0.027
406
c THR092 Thrombophilia Due to Thrombin Defect 74 0.027
407
P RTN024 Retinoblastoma 74 0.027
408
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.027
409
HMN044 Human Immunodeficiency Virus Type 1 73 0.027
410
P HNT016 Huntington Disease 72 0.027
411
PLM001 Pulmonary Tuberculosis 72 0.027
412
MYL009 Myelodysplastic Syndrome 72 0.027
413
P AMY004 Amyloidosis 71 0.027
414
ACR007 Acromegaly 70 0.027
415
P TTR001 Tetralogy of Fallot 70 0.027
416
c ATS007 Autism Spectrum Disorder 69 0.027
417
P MYC084 Mycobacterium Tuberculosis 1 69 0.027
418
P INF038 Influenza 69 0.027
419
OBS002 Obsessive-Compulsive Disorder 69 0.027
420
P ATS364 Autism 68 0.027
421
P SYS005 Systemic Scleroderma 68 0.027
422
GST092 Gastroesophageal Reflux 68 0.027
423
P ASP006 Aspergillosis 67 0.027
424
c FML021 Familial Hypercholesterolemia 67 0.027
425
P THR014 Thrombocytopenia 67 0.027
426
PRT036 Peritonitis 66 0.027
427
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.027
428
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.027
429
P NPH012 Nephrotic Syndrome 65 0.027
430
P PRP019 Peripheral Nervous System Disease 64 0.027
431
SKN016 Skin Disease 64 0.027
432
HMT002 Hematologic Cancer 64 0.027
433
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.027
434
c ACT068 Acute Cystitis 63 0.027
435
OVR029 Ovarian Hyperstimulation Syndrome 63 0.027
436
BLL006 Bullous Pemphigoid 63 0.027
437
P MYP004 Myopathy 63 0.027
438
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.027
439
FTT001 Fatty Liver Disease 63 0.027
440
MDD011 Mood Disorder 62 0.027
441
P RHB003 Rhabdomyosarcoma 62 0.027
442
P LPS004 Lupus Erythematosus 62 0.027
443
P HYP370 Hypokalemic Periodic Paralysis, Type 1 62 0.027
444
P HMN010 Hemangioma 62 0.027
445
P EPD009 Epidermolysis Bullosa Dystrophica 62 0.027
446
NRM005 Neuromuscular Disease 62 0.027
447
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.027
448
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.027
449
CHL068 Cholestasis 61 0.027
450
P URT039 Urticaria 61 0.027
451
P ART023 Arthropathy 61 0.027
452
CTN007 Cutaneous Leishmaniasis 61 0.027
453
NTR005 Nutritional Deficiency Disease 61 0.027
454
MSL001 Measles 61 0.027
455
VRC005 Varicose Veins 61 0.027
456
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.027
457
P CND004 Candidiasis 61 0.027
458
P VNT002 Ventricular Septal Defect 61 0.027
459
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.027
460
CHL123 Chlamydia 60 0.027
461
ALC006 Alcoholic Hepatitis 60 0.027
462
BND020 Bone Disease 60 0.027
463
PLM033 Pulmonary Embolism 60 0.027
464
LPT001 Leptospirosis 60 0.027
465
GST045 Gastroenteritis 60 0.027
466
ADN018 Adenoma 60 0.027
467
P RHN004 Rhinitis 59 0.027
468
P OPT006 Optic Nerve Disease 59 0.027
469
P BRS044 Breast Adenocarcinoma 59 0.027
470
IRN001 Iron Deficiency Anemia 59 0.027
471
P MTR012 Mitral Valve Disease 59 0.027
472
URN010 Urinary Tract Obstruction 59 0.027
473
HDR002 Hidradenitis Suppurativa 58 0.027
474
HYD002 Hydronephrosis 58 0.027
475
IRN002 Iron Metabolism Disease 58 0.027
476
CHL014 Cholera 58 0.027
477
TMT001 Timothy Syndrome 58 0.027
478
P INF037 Inflammatory Bowel Disease 57 0.027
479
P MMP001 Mumps 57 0.027
480
GLL018 Gallbladder Cancer 57 0.027
481
SFT003 Soft Tissue Sarcoma 57 0.027
482
APH002 Aphasia 56 0.027
483
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.027
484
ALL006 Allergic Asthma 56 0.027
485
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.027
486
P MCR010 Microcephaly 56 0.027
487
P PMP001 Pemphigus 56 0.027
488
DBT010 Diabetic Neuropathy 56 0.027
489
MNR012 Meniere Disease 56 0.027
490
P HYP024 Hypoparathyroidism 56 0.027
491
P INT068 Intestinal Disease 56 0.027
492
HRT012 Heart Valve Disease 56 0.027
493
c INT072 Intestinal Pseudo-Obstruction 55 0.027
494
P RST002 Restrictive Cardiomyopathy 55 0.027
495
AMN003 Amnestic Disorder 55 0.027
496
P VNS003 Venous Insufficiency 55 0.027
497
END040 Endogenous Depression 55 0.027
498
LMB002 Lambert-Eaton Myasthenic Syndrome 55 0.027
499
P DYS193 Dystonia 11, Myoclonic 55 0.027
500
P PLY019 Polyneuropathy 55 0.027
501
VSC003 Visceral Leishmaniasis 55 0.027
502
P SML001 Small Cell Carcinoma 55 0.027
503
P LFT003 Left Ventricular Noncompaction 55 0.027
504
RHM028 Rheumatic Heart Disease 54 0.027
505
TRM010 Traumatic Brain Injury 54 0.027
506
P EPD016 Epidermolysis Bullosa 54 0.027
507
PRP016 Paraplegia 54 0.027
508
ZLL002 Zollinger-Ellison Syndrome 54 0.027
509
GTR002 Goiter 54 0.027
510
P ALT001 Alternating Hemiplegia of Childhood 54 0.027
511
P PNC025 Panic Disorder 53 0.027
512
P PTT006 Pituitary Adenoma 53 0.027
513
ALC009 Alcoholic Liver Cirrhosis 53 0.027
514
DYS073 Dysphagia 52 0.027
515
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.027
516
HYP014 Hyperuricemia 52 0.027
517
CHL122 Cholesteatoma of Middle Ear 52 0.027
518
GST037 Gastroparesis 52 0.027
519
PRS021 Prostatic Adenoma 52 0.027
520
KRT009 Keratosis 52 0.027
521
GSG001 Gas Gangrene 52 0.027
522
P HYP077 Hypertrichosis 51 0.027
523
BRN071 Brain Injury 51 0.027
524
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.027
525
HYP080 Hypogonadism 51 0.027
526
LMB062 Limb Ischemia 50 0.027
527
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.027
528
VCC001 Vaccinia 50 0.027
529
TRY001 Trypanosomiasis 50 0.027
530
CRT013 Carotid Stenosis 50 0.027
531
c LNG048 Long Qt Syndrome 3 50 0.027
532
THR016 Thrombophlebitis 50 0.027
533
PLR008 Pleurisy 50 0.027
534
P CTN003 Cutaneous Lupus Erythematosus 50 0.027
535
PRS129 Prostatic Hyperplasia, Benign 49 0.027
536
NTR046 Neutrophil Migration 49 0.027
537
HYP006 Hypertensive Heart Disease 49 0.027
538
P RNV001 Renovascular Hypertension 49 0.027
539
RNL077 Renal Fibrosis 49 0.027
540
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.027
541
GYN001 Gynecomastia 49 0.027
542
CRC014 Carcinoid Tumors, Intestinal 49 0.027
543
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 49 0.027
544
TST015 Testicular Disease 49 0.027
545
SPL018 Splenomegaly 48 0.027
546
c INV001 Invasive Aspergillosis 48 0.027
547
HYP781 Hypoascorbemia 48 0.027
548
INT078 Intracranial Thrombosis 48 0.027
549
P TCL004 T-Cell Leukemia 48 0.027
550
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.027
551
P BLD051 Blood Coagulation Disease 48 0.027
552
VTR007 Vitreoretinopathy 48 0.027
553
c HNT004 Huntington Disease-Like 2 48 0.027
554
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.027
555
P TRT019 Torticollis 48 0.027
556
HDR003 Hidradenitis 48 0.027
557
BRN014 Bronchopneumonia 47 0.027
558
INT010 Intracranial Embolism 47 0.027
559
VTM033 Vitamin K Deficiency Bleeding 47 0.027
560
MGS001 Megaesophagus 47 0.027
561
P MYC033 Myoclonus 47 0.027
562
P BNG032 Benign Mesothelioma 47 0.027
563
ISL001 Islet Cell Tumor 47 0.027
564
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.027
565
TTR005 Tetrahydrobiopterin Deficiency 47 0.027
566
PRP007 Priapism 47 0.027
567
ART004 Aortic Atherosclerosis 47 0.027
568
ANR004 Anuria 47 0.027
569
PLL012 Pollen Allergy 46 0.027
570
c MLG068 Malignant Glioma 46 0.027
571
GRN017 Granulocytopenia 46 0.027
572
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.027
573
c FML008 Familial Retinoblastoma 46 0.027
574
IDP035 Idiopathic Achalasia 46 0.027
575
INT067 Interstitial Nephritis 46 0.027
576
HRN026 Hernia, Hiatus 46 0.027
577
ASP007 Aspiration Pneumonia 46 0.027
578
P RTN014 Retinal Artery Occlusion 46 0.027
579
AVD001 Avoidant Personality Disorder 45 0.027
580
c ACT076 Acute Myocarditis 45 0.027
581
RSP021 Respiratory Allergy 45 0.027
582
CRB090 Cerebral Hypoxia 45 0.027
583
CRV043 Cervical Dystonia 45 0.027
584
RTC009 Reticulum Cell Sarcoma 45 0.027
585
GLC084 Glaucoma, Normal Tension 44 0.027
586
BCK006 Back Pain 44 0.027
587
BCT021 Bacterial Sepsis 44 0.027
588
P BLP003 Blepharospasm 43 0.027
589
LYM052 Lymphomatoid Papulosis 43 0.027
590
P HYP265 Hypotonia 43 0.027
591
LKS001 Leukostasis 43 0.027
592
DST006 Diastolic Heart Failure 43 0.027
593
SBC016 Subacute Delirium 43 0.027
594
ACT088 Acute Insulin Response 42 0.027
595
MYC013 Mycobacterium Abscessus 42 0.027
596
URT037 Urethral Stricture 42 0.027
597
DYS011 Dyskinesia of Esophagus 42 0.027
598
OPD001 Opioid Abuse 42 0.027
599
THR123 Thrombotic Microangiopathy 41 0.027
600
RTN004 Retinal Microaneurysm 41 0.027
601
BRN026 Branch Retinal Artery Occlusion 41 0.027
602
MST004 Mast Cell Neoplasm 40 0.027
603
c CNT028 Central Retinal Artery Occlusion 40 0.027
604
LNR006 Linear Iga Disease 40 0.027
605
HYP064 Hypogonadotropism 40 0.027
606
HYP141 Hyperphenylalaninemia 40 0.027
607
c HMG029 Hemoglobin Se Disease 40 0.027
608
PLT015 Platelet Aggregation, Spontaneous 40 0.027
609
P HMF004 Hemifacial Spasm 40 0.027
610
EST007 Estrogen Resistance 40 0.027
611
SPR126 Superior Semicircular Canal Dehiscence 39 0.027
612
ALD013 Aldosterone-Producing Adenoma 39 0.027
613
HYP264 Hypertonia 39 0.027
614
GNT029 Genetic Hypertension 39 0.027
615
SBV001 Subvalvular Aortic Stenosis 39 0.027
616
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 39 0.027
617
EXT007 Extracutaneous Mastocytoma 39 0.027
618
MYT011 Myotonia 37 0.027
619
AMR003 Amaurosis Fugax 36 0.027
620
HRW001 Hair Whorl 36 0.027
621
CRT008 Carotid Artery Dissection 36 0.027
622
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.027
623
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.027
624
c LKM005 Leukemia, T-Cell, Chronic 35 0.027
625
P FML187 Familial Hypertension 35 0.027
626
INF013 Inferior Myocardial Infarction 35 0.027
628
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.027
629
PPL052 Papillomatosis, Confluent and Reticulated 34 0.027
630
c HMF011 Hemifacial Spasm, Familial 34 0.027
631
PCD001 Pica Disease 33 0.027
632
PRX009 Paroxysmal Hemicrania 33 0.027
633
RRS014 Rare Surgical Neurologic Disease 33 0.027
634
INF021 Infant Gynecomastia 32 0.027
635
P ATR081 Atrial Standstill 29 0.027
636
ARG004 Argyria 28 0.027
637
CHL079 Children's Interstitial Lung Disease 27 0.027
638
SNC001 Sunct Headache 26 0.027
639
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.027
640
ANT078 Antipyrine Metabolism 24 0.027
641
c LNG052 Long Qt Syndrome 8 23 0.027
642
VLK001 Volkmann Contracture 22 0.027
643
P SCN067 Scn1a Seizure Disorders 21 0.027
644
HYP188 Hypnic Headache 21 0.027
645
IDP022 Idiopathic Spinal Cord Herniation 17 0.027
646
c RTN181 Retinitis Pigmentosa 2, X-Linked 16 0.027
647
c RRH030 Rare Headache 16 0.027
648
c SCN066 Secondary Erythromelalgia 13 0.027
Content
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