Search results for Verapamil

643 hits were found for Verapamil

# Family MCID Name MIFTS Score
1
ANG054 Angina Pectoris 66 0.361
2
c HYP595 Hypertension, Essential 84 0.323
3
P ATR011 Atrial Fibrillation 66 0.273
4
P HYP061 Hypertrophic Cardiomyopathy 70 0.261
5
c ACT075 Acute Myocardial Infarction 57 0.258
6
c ATR087 Atrial Standstill 1 75 0.252
7
ATR057 Atrioventricular Block 55 0.244
8
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.208
9
P MYC007 Myocardial Infarction 70 0.194
10
CNG034 Congestive Heart Failure 69 0.181
11
LPP008 Lipoprotein Quantitative Trait Locus 62 0.181
12
ISC004 Ischemia 58 0.179
13
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.177
14
CNS004 Constipation 58 0.177
15
c PYR010 Peyronie's Disease 50 0.164
16
P KDN018 Kidney Disease 72 0.162
17
P HDC001 Headache 57 0.162
18
ART140 Arteries, Anomalies of 52 0.162
19
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.160
20
INT007 Intermediate Coronary Syndrome 55 0.158
21
P CRD119 Cardiac Arrest 67 0.155
22
c MGR028 Migraine with or Without Aura 1 67 0.148
23
P CLS010 Cluster Headache 42 0.146
24
WLF001 Wolff-Parkinson-White Syndrome 66 0.144
25
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.141
26
RGH001 Right Bundle Branch Block 48 0.141
27
CRD137 Cardiogenic Shock 47 0.136
28
P PLM037 Pulmonary Hypertension 67 0.133
29
IMP005 Impotence 52 0.125
30
48X005 48,xyyy 39 0.125
31
P HRT032 Heart Disease 75 0.122
32
KLD004 Keloid Disorder 40 0.119
33
c ACT071 Acute Kidney Failure 60 0.116
34
HYP266 Hypoxia 57 0.116
35
P SZR006 Seizure Disorder 56 0.116
36
HYP056 Hypoglycemia 66 0.113
37
RST023 Resting Heart Rate, Variation in 41 0.113
38
c DLT002 Dilated Cardiomyopathy 79 0.110
39
VSL002 Visual Epilepsy 59 0.110
40
P EPL164 Epilepsy 71 0.107
41
CRD223 Cardiac Arrhythmia 60 0.107
42
P BLD134 Bladder Cancer 79 0.103
43
P TRN020 Turner Syndrome 67 0.103
44
ATH013 Atherosclerosis Susceptibility 65 0.103
45
DPR016 Depression 63 0.103
46
LVR012 Liver Cirrhosis 62 0.103
47
SYN036 Syncope 45 0.103
48
STR067 Stroke, Ischemic 81 0.100
49
P CRN300 Coronary Heart Disease 1 63 0.100
50
HYP066 Hyperglycemia 61 0.100
51
HYP457 Hypertrophic Scars 42 0.100
52
ATR089 Atrioventricular Dissociation 20 0.096
53
CRB039 Cerebrovascular Disease 67 0.092
54
P LNG028 Long Qt Syndrome 66 0.092
55
ALL026 Allergic Hypersensitivity Disease 62 0.092
56
HYP020 Hyperprolactinemia 64 0.088
57
STT001 Status Epilepticus 60 0.088
58
PRT013 Portal Hypertension 59 0.088
59
MTB004 Metabolic Acidosis 50 0.088
60
SCN049 Second-Degree Atrioventricular Block 35 0.088
61
P OVR042 Ovarian Cancer 88 0.084
62
c FML001 Familial Atrial Fibrillation 65 0.084
63
CLN015 Colon Adenocarcinoma 65 0.084
64
P DBT009 Diabetes Mellitus 64 0.084
65
HYP005 Hypokalemia 55 0.084
66
P SCK002 Sick Sinus Syndrome 55 0.084
67
PNG002 Pain Agnosia 51 0.084
68
MYL069 Myeloma, Multiple 85 0.080
69
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.080
70
P LKM002 Leukemia 68 0.080
71
P VSC007 Vascular Disease 63 0.080
72
P HYP069 Hyperparathyroidism 63 0.080
73
CMR002 Coumarin Resistance 56 0.080
74
PLM010 Pulmonary Edema 54 0.080
75
LFT001 Left Bundle Branch Hemiblock 49 0.080
76
CRN019 Coronary Artery Vasospasm 46 0.080
77
AST005 Asthma 76 0.075
78
P SCH015 Schizophrenia 74 0.075
79
P MSC005 Muscular Dystrophy 66 0.075
80
P GLM045 Glioma 63 0.075
81
P MYC008 Myocarditis 59 0.075
82
P DDN001 Duodenal Ulcer 52 0.075
83
GLL048 Glial Tumor 45 0.075
84
CYT002 Cytokine Deficiency 42 0.075
85
P CLR023 Colorectal Cancer 99 0.071
86
P LNG032 Lung Cancer 98 0.071
87
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.071
88
P RSP003 Respiratory Failure 74 0.071
89
c CHR684 Chronic Kidney Disease 70 0.071
90
c SML038 Small Cell Cancer of the Lung 65 0.071
91
P ADN016 Adenocarcinoma 64 0.071
92
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.071
93
c ACT027 Acute Pancreatitis 60 0.071
94
LNG099 Lung Disease 60 0.071
95
P EXN002 Exanthem 57 0.071
96
P CRD246 Cardiovascular System Disease 57 0.071
97
HYP060 Hyperinsulinism 54 0.071
98
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
99
BHR001 Behr Syndrome 51 0.071
100
P RNL015 Renal Hypertension 47 0.071
101
c MCR120 Microvascular Complications of Diabetes 7 47 0.071
102
THR099 Third-Degree Atrioventricular Block 45 0.071
103
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.071
104
ATX019 Ataxia with Vitamin E Deficiency 42 0.071
105
c MCR130 Microvascular Complications of Diabetes 6 41 0.071
106
c MCR133 Microvascular Complications of Diabetes 4 41 0.071
107
ANX004 Anoxia 40 0.071
108
MLT131 Multifocal Atrial Tachycardia 18 0.071
109
P BRS047 Breast Cancer 97 0.065
110
GLB015 Glioblastoma Multiforme 75 0.065
111
c HYP836 Hypercholesterolemia, Familial, 1 73 0.065
112
P NRB001 Neuroblastoma 72 0.065
113
PRP027 Peripheral Vascular Disease 71 0.065
114
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.065
115
P LKM062 Leukemia, Acute Lymphoblastic 69 0.065
116
P NTR004 Neutropenia 63 0.065
117
P MYL006 Myeloid Leukemia 60 0.065
118
P CTR002 Cataract 60 0.065
119
PRT058 Pure Autonomic Failure 59 0.065
120
P BPL003 Bipolar Disorder 56 0.065
121
P NRP001 Neuropathy 56 0.065
122
P DRR001 Diarrhea 55 0.065
123
P HYP076 Hyperthyroidism 55 0.065
124
TRD006 Tardive Dyskinesia 54 0.065
125
GLC003 Glucose Intolerance 54 0.065
126
P OVR082 Overgrowth Syndrome 50 0.065
127
RYN005 Raynaud Phenomenon 47 0.065
128
c MJR024 Major Affective Disorder 9 41 0.065
129
HYP540 Hypertension, Diastolic 40 0.065
130
c MJR022 Major Affective Disorder 8 38 0.065
131
P HPT023 Hepatocellular Carcinoma 100 0.060
132
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.060
133
P LKM071 Leukemia, Chronic Lymphocytic 79 0.060
134
OST012 Osteoarthritis 78 0.060
135
c MNN043 Meningioma, Familial 74 0.060
136
c LKM063 Leukemia, Chronic Myeloid 72 0.060
137
ADL002 Adult Syndrome 70 0.060
138
P HYP086 Hypothyroidism 69 0.060
139
OST159 Osteogenic Sarcoma 66 0.060
140
P MCR115 Microvascular Complications of Diabetes 5 66 0.060
141
CHG001 Chagas Disease 66 0.060
142
TTN003 Tetanus 65 0.060
143
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.060
144
c DBT099 Diabetes Mellitus, Type I 65 0.060
145
TRN015 Transient Cerebral Ischemia 63 0.060
146
ERL001 Early Myoclonic Encephalopathy 62 0.060
147
LPD008 Lipid Metabolism Disorder 62 0.060
148
CLT003 Colitis 62 0.060
149
MNN042 Meningioma, Radiation-Induced 62 0.060
150
INT002 Intermittent Claudication 61 0.060
151
PPT005 Peptic Ulcer Disease 59 0.060
152
ERY003 Erythema Multiforme 58 0.060
153
CMM005 Common Cold 57 0.060
154
P ART021 Arteriosclerosis 54 0.060
155
GNG012 Gingival Overgrowth 51 0.060
156
END086 End Stage Renal Disease 51 0.060
157
SPN021 Spinal Meningioma 50 0.060
158
P MTR003 Mitral Valve Stenosis 50 0.060
159
STM007 Stomatitis 50 0.060
160
P TMP001 Temporal Lobe Epilepsy 50 0.060
161
TST044 Testicular Torsion 47 0.060
162
ACT003 Acute Kidney Tubular Necrosis 45 0.060
163
c PRM038 Primary Agammaglobulinemia 44 0.060
164
SCR001 Secretory Meningioma 41 0.060
165
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.060
166
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.060
167
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.060
168
c LKM061 Leukemia, Acute Myeloid 84 0.053
169
P PNC035 Pancreatic Cancer 84 0.053
170
P MDL005 Medulloblastoma 77 0.053
171
MRF001 Marfan Syndrome 77 0.053
172
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.053
173
CRH001 Crohn's Disease 74 0.053
174
ANX010 Anxiety 73 0.053
175
MSC157 Muscular Dystrophy, Duchenne Type 72 0.053
176
DFC004 Deficiency Anemia 70 0.053
177
LYM133 Lymphoma, Hodgkin, Classic 69 0.053
178
P MYS003 Myasthenia Gravis 68 0.053
179
P MLG056 Malignant Hyperthermia 67 0.053
180
c MCR129 Microvascular Complications of Diabetes 1 66 0.053
181
IRR002 Irritable Bowel Syndrome 65 0.053
182
P VSC011 Vasculitis 62 0.053
183
P ORT004 Orthostatic Intolerance 62 0.053
184
INS001 Insulinoma 60 0.053
185
P OPT006 Optic Nerve Disease 60 0.053
186
c ACT073 Acute Leukemia 58 0.053
187
CRD132 Cardiac Conduction Defect 58 0.053
188
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.053
189
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.053
190
P ALP008 Alopecia 54 0.053
191
FCL014 Focal Epilepsy 54 0.053
192
STT041 Stuttering 52 0.053
193
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.053
194
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.053
195
c SCN007 Secondary Hyperparathyroidism 51 0.053
196
CRN030 Coronary Stenosis 50 0.053
197
47X002 47,xyy 49 0.053
198
SNT005 Sinoatrial Node Disease 49 0.053
199
URM002 Uremia 49 0.053
200
BNR002 Bone Resorption Disease 48 0.053
201
WTH001 Withdrawal Disorder 48 0.053
202
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.053
203
HLX001 Helix Syndrome 47 0.053
204
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.053
205
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.053
206
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.053
207
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.053
208
URT010 Ureteral Obstruction 45 0.053
209
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.053
210
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.053
211
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.053
212
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.053
213
P MJR007 Major Affective Disorder 1 43 0.053
214
c MCR112 Microvascular Complications of Diabetes 2 41 0.053
215
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.053
216
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 31 0.053
217
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.053
218
INT053 Intracranial Vasospasm 24 0.053
219
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.046
220
P ALZ034 Alzheimer Disease 88 0.046
221
P GST053 Gastric Cancer 83 0.046
222
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.046
223
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.046
224
BRN028 Brain Cancer 74 0.046
225
SCK003 Sickle Cell Anemia 74 0.046
226
LPT014 Leptin Deficiency or Dysfunction 74 0.046
227
ULC004 Ulcerative Colitis 73 0.046
228
P PHC003 Pheochromocytoma 71 0.046
229
P BRG001 Brugada Syndrome 71 0.046
230
P SRC025 Sarcoidosis 1 70 0.046
231
DWN001 Down Syndrome 70 0.046
232
PLY001 Polycythemia Vera 69 0.046
233
SVR097 Severe Cutaneous Adverse Reaction 69 0.046
234
P LYM118 Lymphoma 68 0.046
235
P LVR013 Liver Disease 68 0.046
236
P ESS003 Essential Thrombocythemia 68 0.046
237
c INF071 Inflammatory Bowel Disease 1 67 0.046
238
THY111 Thyroid Carcinoma, Familial Medullary 67 0.046
239
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.046
240
P DYS154 Dystonia 65 0.046
241
PRT037 Pertussis 65 0.046
242
P ADL010 Adult Respiratory Distress Syndrome 65 0.046
243
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.046
244
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.046
245
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.046
246
c PRC016 Pre-Eclampsia 63 0.046
247
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.046
248
HYD038 Hydrops Fetalis, Nonimmune 62 0.046
249
TXC005 Toxic Shock Syndrome 62 0.046
250
NTR005 Nutritional Deficiency Disease 62 0.046
251
P ENC018 Encephalopathy 61 0.046
252
THY029 Thyroid Carcinoma 59 0.046
253
GNG013 Gingivitis 59 0.046
254
c PRM005 Primary Hyperparathyroidism 58 0.046
255
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.046
256
MNT002 Mental Depression 58 0.046
257
HMR039 Hemorrhage, Intracerebral 57 0.046
258
LNN001 Lennox-Gastaut Syndrome 57 0.046
259
P PLY018 Polycythemia 56 0.046
260
ALL006 Allergic Asthma 56 0.046
261
ERY051 Erythroleukemia, Familial 56 0.046
262
c GRV008 Graves Disease 1 56 0.046
263
AGN016 Aging 56 0.046
264
MRD002 Marden-Walker Syndrome 56 0.046
265
CRC006 Carcinoid Syndrome 55 0.046
266
HMP005 Hemiplegia 55 0.046
267
P LTR001 Lateral Sclerosis 54 0.046
268
P FML023 Familial Hemiplegic Migraine 53 0.046
269
CRH005 Crohn's Colitis 53 0.046
270
OCL006 Ocular Hypertension 53 0.046
271
TXC002 Toxic Encephalopathy 53 0.046
272
c FML191 Familial Long Qt Syndrome 53 0.046
273
ART074 Aortic Dissection 52 0.046
274
OCL069 Ocular Motor Apraxia 51 0.046
275
c PRM012 Primary Polycythemia 50 0.046
276
c SVR005 Severe Pre-Eclampsia 50 0.046
277
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.046
278
P SCK005 Sickle Cell Disease 50 0.046
279
THY125 Thyroid Gland Medullary Carcinoma 50 0.046
280
c THR090 Thrombocythemia 1 49 0.046
281
SYS003 Systolic Heart Failure 49 0.046
282
P OPN001 Open-Angle Glaucoma 49 0.046
283
BRN071 Brain Injury 49 0.046
284
P CMP008 Compartment Syndrome 49 0.046
285
c MTR002 Mitral Valve Insufficiency 48 0.046
286
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.046
287
PRL017 Prolymphocytic Leukemia 47 0.046
288
DRG003 Drug Dependence 47 0.046
289
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.046
290
LYM019 Lymphosarcoma 46 0.046
291
ATN005 Autonomic Dysfunction 46 0.046
292
MYC005 Myocardial Stunning 46 0.046
293
ADR040 Adrenal Gland Pheochromocytoma 46 0.046
294
CRB004 Cerebral Artery Occlusion 45 0.046
295
CNT017 Central Nervous System Origin Vertigo 45 0.046
296
DMP001 Dumping Syndrome 44 0.046
297
CVD001 Covid-19 44 0.046
298
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 43 0.046
299
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.046
300
DRG024 Drug Allergy 42 0.046
301
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.046
302
RDN001 Reading Disorder 40 0.046
303
PRM020 Premenstrual Tension 40 0.046
304
CRB086 Cerebral Aneurysms 40 0.046
305
P INT260 Intracranial Berry Aneurysm 39 0.046
306
P DYS021 Dysautonomia 39 0.046
307
FRS012 First-Degree Atrioventricular Block 38 0.046
308
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 35 0.046
309
P MYC026 Myoclonus Epilepsy 35 0.046
310
c MJR008 Major Affective Disorder 2 35 0.046
311
c MJR023 Major Affective Disorder 7 33 0.046
312
c MJR003 Major Affective Disorder 6 33 0.046
313
c MJR006 Major Affective Disorder 5 33 0.046
314
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.046
315
ERY066 Erythema Multiforme Major 30 0.046
316
c MJR004 Major Affective Disorder 4 28 0.046
317
CYT018 Cytochrome P450 2d6 Variant 27 0.046
318
c PRC045 Preeclampsia/eclampsia 5 25 0.046
319
c PRC034 Preeclampsia/eclampsia 4 23 0.046
320
HDG004 Hodgkin's Granuloma 23 0.046
321
HDG006 Hodgkin's Paragranuloma 22 0.046
322
GST040 Gastric Adenocarcinoma 70 0.038
323
ADN011 Adenoid Cystic Carcinoma 70 0.038
324
ART016 Aortic Aneurysm 69 0.038
325
MNT001 Mantle Cell Lymphoma 69 0.038
326
PNC129 Pancreatic Adenocarcinoma 68 0.038
327
P HPT021 Hepatitis 67 0.038
328
ALL003 Allergic Rhinitis 67 0.038
329
c RHB024 Rhabdomyosarcoma 2 67 0.038
330
P HRP006 Herpes Simplex 65 0.038
331
P PRS038 Personality Disorder 65 0.038
332
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.038
333
LSH001 Leishmaniasis 63 0.038
334
P MVM001 Movement Disease 63 0.038
335
P END044 Endometriosis 63 0.038
336
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.038
337
c SVR001 Severe Acute Respiratory Syndrome 62 0.038
338
P HYP750 Hypertriglyceridemia, Familial 62 0.038
339
CRC021 Carcinosarcoma 62 0.038
340
c SCL052 Scleroderma, Familial Progressive 61 0.038
341
P PNC044 Pancreatitis 61 0.038
342
VRL011 Viral Infectious Disease 61 0.038
343
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.038
344
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.038
345
P MYM013 Moyamoya Disease 1 57 0.038
346
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.038
347
BRD001 Brody Myopathy 57 0.038
348
THR024 Thrombosis 57 0.038
349
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.038
350
P FBR017 Fibrosarcoma 56 0.038
351
TRN018 Transitional Cell Carcinoma 56 0.038
352
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.038
353
MCS002 Mucositis 56 0.038
354
NPH009 Nephrolithiasis 55 0.038
355
P SBS003 Substance Abuse 55 0.038
356
P DBT005 Diabetes Insipidus 55 0.038
357
PRP030 Purpura 54 0.038
358
HMS001 Hemosiderosis 54 0.038
359
P TRM003 Tremor 54 0.038
360
PRS045 Prostatic Hypertrophy 53 0.038
361
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.038
362
INT075 Intracranial Hypertension 53 0.038
363
GST023 Gastric Ulcer 53 0.038
364
PRP080 Peripheral Artery Disease 53 0.038
365
TLN003 Telangiectasis 52 0.038
366
NPH003 Nephrocalcinosis 51 0.038
367
ACH005 Achalasia 51 0.038
368
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.038
369
P ECL001 Eclampsia 50 0.038
370
OPT003 Opiate Dependence 50 0.038
371
P RNV001 Renovascular Hypertension 48 0.038
372
OPD006 Opioid Addiction 48 0.038
373
MLT006 Multidrug-Resistant Tuberculosis 48 0.038
374
SXL003 Sexual Disorder 47 0.038
375
P ERY008 Erythromelalgia 47 0.038
376
TST014 Testicular Cancer 46 0.038
377
MCR191 Microscopic Colitis 46 0.038
378
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.038
379
P PRD021 Periodic Paralysis 45 0.038
380
CRT015 Carotid Artery Occlusion 45 0.038
381
PTT037 Pituitary Tumors 44 0.038
382
SKN005 Skin Atrophy 43 0.038
383
PLY068 Polysubstance Abuse 43 0.038
384
GLC096 Galactorrhea 42 0.038
385
P KLZ004 Kala-Azar 1 41 0.038
386
P RRH023 Rare Hereditary Hemochromatosis 41 0.038
387
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.038
388
ANG049 Angioedema Induced by Ace Inhibitors 40 0.038
389
DBT007 Diabetic Cataract 38 0.038
390
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.038
391
OVR094 Ovarian Epithelial Cancer 38 0.038
392
c HNT011 Huntington Disease-Like 3 38 0.038
393
KDN013 Kidney Hypertrophy 32 0.038
394
c SPR083 Sporadic Hemiplegic Migraine 29 0.038
395
HMC012 Hemicrania Continua 28 0.038
396
ACT118 Acute Non Lymphoblastic Leukemia 26 0.038
397
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.038
398
BDR001 Bidirectional Tachycardia 19 0.038
399
MLR004 Malaria 81 0.027
400
P GLM040 Glioma Susceptibility 1 81 0.027
401
CRV035 Cervical Cancer 76 0.027
402
c THR092 Thrombophilia Due to Thrombin Defect 73 0.027
403
P RTN024 Retinoblastoma 73 0.027
404
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.027
405
P HNT016 Huntington Disease 72 0.027
406
ACR007 Acromegaly 71 0.027
407
HMN044 Human Immunodeficiency Virus Type 1 71 0.027
408
P ATS364 Autism 70 0.027
409
P AMY004 Amyloidosis 70 0.027
410
MYL009 Myelodysplastic Syndrome 70 0.027
411
P TTR001 Tetralogy of Fallot 70 0.027
412
P MYP004 Myopathy 70 0.027
413
P ASP006 Aspergillosis 69 0.027
414
PLM001 Pulmonary Tuberculosis 69 0.027
415
P MLN008 Melanoma 69 0.027
416
P SYS005 Systemic Scleroderma 68 0.027
417
P MYC084 Mycobacterium Tuberculosis 1 68 0.027
418
OBS002 Obsessive-Compulsive Disorder 68 0.027
419
P INF038 Influenza 68 0.027
420
P THR014 Thrombocytopenia 67 0.027
421
GST092 Gastroesophageal Reflux 67 0.027
422
c ATS007 Autism Spectrum Disorder 67 0.027
423
LPT001 Leptospirosis 66 0.027
424
c FML021 Familial Hypercholesterolemia 66 0.027
425
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.027
426
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.027
427
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.027
428
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.027
429
NRM005 Neuromuscular Disease 64 0.027
430
OVR029 Ovarian Hyperstimulation Syndrome 64 0.027
431
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.027
432
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.027
433
P RHB003 Rhabdomyosarcoma 63 0.027
434
SKN016 Skin Disease 63 0.027
435
c ACT068 Acute Cystitis 63 0.027
436
HMT002 Hematologic Cancer 62 0.027
437
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.027
438
BLL006 Bullous Pemphigoid 62 0.027
439
P ART023 Arthropathy 62 0.027
440
ATM095 Autoimmune Disease 62 0.027
441
CTN007 Cutaneous Leishmaniasis 62 0.027
442
MDD011 Mood Disorder 62 0.027
443
MSL001 Measles 62 0.027
444
CHL068 Cholestasis 61 0.027
445
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.027
446
FTT001 Fatty Liver Disease 61 0.027
447
TMT001 Timothy Syndrome 61 0.027
448
ALC006 Alcoholic Hepatitis 61 0.027
449
P LPS004 Lupus Erythematosus 61 0.027
450
P HMN010 Hemangioma 61 0.027
451
P NPH012 Nephrotic Syndrome 60 0.027
452
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.027
453
P VNT002 Ventricular Septal Defect 60 0.027
454
VRC005 Varicose Veins 60 0.027
455
HYD002 Hydronephrosis 60 0.027
456
P MCR010 Microcephaly 59 0.027
457
CHL014 Cholera 59 0.027
458
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.027
459
P BND020 Bone Disease 59 0.027
460
CHL123 Chlamydia 59 0.027
461
PLM033 Pulmonary Embolism 59 0.027
462
P BRS044 Breast Adenocarcinoma 59 0.027
463
IRN001 Iron Deficiency Anemia 59 0.027
464
GST045 Gastroenteritis 59 0.027
465
ANR040 Aneurysm 59 0.027
466
P BCL017 B-Cell Lymphoma 58 0.027
467
P URT039 Urticaria 58 0.027
468
P MTR012 Mitral Valve Disease 58 0.027
469
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.027
470
P MMP001 Mumps 58 0.027
471
P CND004 Candidiasis 58 0.027
472
P PRP019 Peripheral Nervous System Disease 58 0.027
473
P GLL018 Gallbladder Cancer 57 0.027
474
IRN002 Iron Metabolism Disease 57 0.027
475
MNR012 Meniere Disease 57 0.027
476
P RHN004 Rhinitis 57 0.027
477
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.027
478
APH002 Aphasia 57 0.027
479
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.027
480
c INT072 Intestinal Pseudo-Obstruction 56 0.027
481
SFT003 Soft Tissue Sarcoma 56 0.027
482
ISL001 Islet Cell Tumor 56 0.027
483
P HYP024 Hypoparathyroidism 56 0.027
484
P RST002 Restrictive Cardiomyopathy 56 0.027
485
P PLY019 Polyneuropathy 56 0.027
486
LMB062 Limb Ischemia 55 0.027
487
ZLL002 Zollinger-Ellison Syndrome 55 0.027
488
VSC003 Visceral Leishmaniasis 55 0.027
489
P DYS193 Dystonia 11, Myoclonic 55 0.027
490
P PTT006 Pituitary Adenoma 55 0.027
491
ACT058 Active Peptic Ulcer Disease 55 0.027
492
HDR002 Hidradenitis Suppurativa 55 0.027
493
P VNS003 Venous Insufficiency 55 0.027
494
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.027
495
URN010 Urinary Tract Obstruction 55 0.027
496
END040 Endogenous Depression 55 0.027
497
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.027
498
P PMP001 Pemphigus 54 0.027
499
P LFT003 Left Ventricular Noncompaction 54 0.027
500
AMN003 Amnestic Disorder 54 0.027
501
GST037 Gastroparesis 54 0.027
502
BRN014 Bronchopneumonia 54 0.027
503
P INF037 Inflammatory Bowel Disease 54 0.027
504
DBT010 Diabetic Neuropathy 54 0.027
505
c LNG048 Long Qt Syndrome 3 53 0.027
506
P EPD016 Epidermolysis Bullosa 53 0.027
507
RHM028 Rheumatic Heart Disease 53 0.027
508
HRT012 Heart Valve Disease 53 0.027
509
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.027
510
P MNC007 Monocytic Leukemia 53 0.027
511
P ALT001 Alternating Hemiplegia of Childhood 53 0.027
512
P CTN003 Cutaneous Lupus Erythematosus 53 0.027
513
GTR002 Goiter 53 0.027
514
GSG001 Gas Gangrene 53 0.027
515
P PNC025 Panic Disorder 53 0.027
516
c FML008 Familial Retinoblastoma 53 0.027
517
ALC009 Alcoholic Liver Cirrhosis 53 0.027
518
P INT068 Intestinal Disease 53 0.027
519
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.027
520
PRP016 Paraplegia 52 0.027
521
P SML001 Small Cell Carcinoma 52 0.027
522
HYP014 Hyperuricemia 52 0.027
523
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.027
524
AVD001 Avoidant Personality Disorder 51 0.027
525
PRS021 Prostatic Adenoma 51 0.027
526
KRT009 Keratosis 51 0.027
527
THR016 Thrombophlebitis 51 0.027
528
TRM010 Traumatic Brain Injury 51 0.027
529
HYP781 Hypoascorbemia 51 0.027
530
P HYP077 Hypertrichosis 50 0.027
531
PLR008 Pleurisy 50 0.027
532
c HNT004 Huntington Disease-Like 2 50 0.027
533
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.027
534
HPT014 Hepatorenal Syndrome 50 0.027
535
CHL122 Cholesteatoma of Middle Ear 50 0.027
536
CRT013 Carotid Stenosis 50 0.027
537
TRY001 Trypanosomiasis 50 0.027
538
NTR046 Neutrophil Migration 50 0.027
539
DYS073 Dysphagia 50 0.027
540
HYP080 Hypogonadism 50 0.027
541
HYP006 Hypertensive Heart Disease 49 0.027
542
GYN001 Gynecomastia 49 0.027
543
HDR003 Hidradenitis 49 0.027
544
PRS129 Prostatic Hyperplasia, Benign 49 0.027
545
INT078 Intracranial Thrombosis 49 0.027
546
c INV001 Invasive Aspergillosis 49 0.027
547
VCC001 Vaccinia 49 0.027
548
ATS010 Autosomal Recessive Disease 48 0.027
549
ASP007 Aspiration Pneumonia 48 0.027
550
VTM033 Vitamin K Deficiency Bleeding 48 0.027
551
INT067 Interstitial Nephritis 48 0.027
552
SPL018 Splenomegaly 48 0.027
553
INT010 Intracranial Embolism 48 0.027
554
P TRT019 Torticollis 48 0.027
555
ART004 Aortic Atherosclerosis 47 0.027
556
PRP007 Priapism 47 0.027
557
HRN026 Hernia, Hiatus 47 0.027
558
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.027
559
CRC014 Carcinoid Tumors, Intestinal 47 0.027
560
RNL077 Renal Fibrosis 47 0.027
561
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.027
562
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.027
563
P RTN014 Retinal Artery Occlusion 47 0.027
564
P BLD051 Blood Coagulation Disease 46 0.027
565
P VTR007 Vitreoretinopathy 46 0.027
566
c ACT076 Acute Myocarditis 46 0.027
567
PLL012 Pollen Allergy 46 0.027
568
P BNG032 Benign Mesothelioma 46 0.027
569
P MYC033 Myoclonus 46 0.027
570
LKS001 Leukostasis 46 0.027
571
OPD001 Opioid Abuse 46 0.027
572
GLC084 Glaucoma, Normal Tension 46 0.027
573
c DRR009 Diarrhea 6 46 0.027
574
ANR004 Anuria 46 0.027
575
c MLG068 Malignant Glioma 46 0.027
576
TTR005 Tetrahydrobiopterin Deficiency 45 0.027
577
RSP021 Respiratory Allergy 45 0.027
578
URL001 Urolithiasis 45 0.027
579
SBC016 Subacute Delirium 44 0.027
580
GRN017 Granulocytopenia 44 0.027
581
IMM064 Immunodeficiency, Common Variable, 10 44 0.027
582
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.027
583
P BLP003 Blepharospasm 44 0.027
584
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.027
585
BCT021 Bacterial Sepsis 44 0.027
586
CRB090 Cerebral Hypoxia 44 0.027
587
TST015 Testicular Disease 43 0.027
588
URT037 Urethral Stricture 43 0.027
589
RTC009 Reticulum Cell Sarcoma 43 0.027
590
MGS001 Megaesophagus 43 0.027
591
MYC013 Mycobacterium Abscessus 43 0.027
592
c CNT028 Central Retinal Artery Occlusion 43 0.027
593
P HYP265 Hypotonia 43 0.027
594
MST004 Mast Cell Neoplasm 42 0.027
595
CRV043 Cervical Dystonia 42 0.027
596
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 41 0.027
597
DYS011 Dyskinesia of Esophagus 41 0.027
598
EST007 Estrogen Resistance 41 0.027
599
PCD001 Pica Disease 41 0.027
600
ACT088 Acute Insulin Response 41 0.027
601
LNR006 Linear Iga Disease 40 0.027
602
BRN026 Branch Retinal Artery Occlusion 40 0.027
603
SPR126 Superior Semicircular Canal Dehiscence 40 0.027
604
ALD013 Aldosterone-Producing Adenoma 39 0.027
605
HYP141 Hyperphenylalaninemia 39 0.027
606
c HMG029 Hemoglobin Se Disease 39 0.027
607
EXT007 Extracutaneous Mastocytoma 38 0.027
608
HYP264 Hypertonia 38 0.027
609
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.027
610
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.027
611
LYM052 Lymphomatoid Papulosis 38 0.027
612
P HMF004 Hemifacial Spasm 38 0.027
613
c CRD087 Cardiomyopathy, Familial Hypertrophic, 10 37 0.027
614
P FML187 Familial Hypertension 37 0.027
615
P PYR039 Peyronie Disease 36 0.027
617
THR123 Thrombotic Microangiopathy 36 0.027
618
HRW001 Hair Whorl 36 0.027
619
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.027
620
MYT011 Myotonia 34 0.027
621
AMR003 Amaurosis Fugax 34 0.027
622
c LKM005 Leukemia, T-Cell, Chronic 34 0.027
623
CRT008 Carotid Artery Dissection 33 0.027
624
PPL052 Papillomatosis, Confluent and Reticulated 33 0.027
625
PRX009 Paroxysmal Hemicrania 33 0.027
626
RTN004 Retinal Microaneurysm 33 0.027
627
c HMF011 Hemifacial Spasm, Familial 33 0.027
628
SBV001 Subvalvular Aortic Stenosis 33 0.027
629
INF013 Inferior Myocardial Infarction 33 0.027
630
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.027
631
INF021 Infant Gynecomastia 31 0.027
632
SNC001 Sunct Headache 29 0.027
633
P ATR081 Atrial Standstill 28 0.027
634
ARG004 Argyria 27 0.027
635
c LNG052 Long Qt Syndrome 8 27 0.027
636
P PRX010 Paroxysmal Ventricular Fibrillation 25 0.027
637
VLK001 Volkmann Contracture 25 0.027
638
ANT078 Antipyrine Metabolism 24 0.027
639
SCN067 Scn1a Seizure Disorders 19 0.027
640
NNN035 Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome 18 0.027
641
IDP022 Idiopathic Spinal Cord Herniation 17 0.027
642
c RRH030 Rare Headache 15 0.027
643
c SCN066 Secondary Erythromelalgia 12 0.027
Content
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