Search results for Propranolol

835 hits were found for Propranolol

# Family MCID Name MIFTS Score
1
P HMN010 Hemangioma 59 0.205
2
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.135
3
P CPL006 Capillary Hemangioma 51 0.097
4
P PRT013 Portal Hypertension 60 0.094
5
PST028 Post-Traumatic Stress Disorder 57 0.094
6
ACT084 Acute Stress Disorder 40 0.094
7
LVR012 Liver Cirrhosis 67 0.091
8
VSC006 Vascular Cancer 51 0.091
9
ESP023 Esophageal Disease 54 0.089
10
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.086
11
P LVR013 Liver Disease 75 0.082
12
DSS008 Disease of Mental Health 52 0.082
13
VSC009 Vascular Skin Disease 19 0.082
14
c HYP595 Hypertension, Essential 69 0.079
15
ANX002 Anxiety Disorder 67 0.079
16
ESP002 Esophageal Varix 41 0.079
17
DRG001 Drug Psychosis 38 0.079
18
END072 Endotheliitis 42 0.076
19
c HMN027 Hemangioma, Capillary Infantile 41 0.076
20
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.076
21
c CRN214 Coronary Heart Disease 5 22 0.076
22
P HRT032 Heart Disease 75 0.072
23
P CRN178 Coronary Heart Disease 6 21 0.072
24
P HPT021 Hepatitis 69 0.069
25
RTN018 Retinal Disease 53 0.069
26
ACT058 Active Peptic Ulcer Disease 43 0.069
27
SKN018 Skin Hemangioma 39 0.069
28
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.069
29
PLC008 Placenta Disease 33 0.069
30
PSY004 Psychotic Disorder 67 0.065
31
EYD002 Eye Disease 61 0.065
32
c ESS001 Essential Tremor 59 0.065
33
c EXD008 Exudative Vitreoretinopathy 1 59 0.065
34
ETH011 Ethylmalonic Encephalopathy 56 0.065
35
GST050 Gastrointestinal System Disease 56 0.065
36
BRN106 Burns 52 0.065
37
P RNL015 Renal Hypertension 48 0.065
38
VND001 Vein Disease 47 0.065
39
PRP021 Peripheral Nervous System Neoplasm 46 0.065
40
ADR038 Adermatoglyphia 46 0.065
41
VSC047 Vascular Malformation 45 0.065
42
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.065
43
CPL005 Capillary Disease 36 0.065
44
STR005 Stork Bite 13 0.065
45
P MYP004 Myopathy 67 0.060
46
c CNT035 Central Nervous System Disease 60 0.060
47
P ENC018 Encephalopathy 59 0.060
48
c PND001 Pain Disorder 54 0.060
49
P MSC033 Muscle Disorders 52 0.060
50
ATR060 Atrial Standstill, Digenic 51 0.060
51
STM006 Stomach Disease 50 0.060
52
MGR028 Migraine with or Without Aura 1 47 0.060
53
AYM001 Ayme-Gripp Syndrome 41 0.060
54
ATN003 Autonomic Nervous System Neoplasm 40 0.060
55
GLB003 Globe Disease 32 0.060
56
P MYC007 Myocardial Infarction 79 0.056
57
CNG034 Congestive Heart Failure 72 0.056
58
P NRV007 Nervous System Disease 71 0.056
59
PRP027 Peripheral Vascular Disease 68 0.056
60
MTH009 Mouth Disease 61 0.056
61
RTN017 Retinal Detachment 56 0.056
62
HDC001 Headache 54 0.056
63
SLP005 Sleep Disorder 53 0.056
64
GNR004 Generalized Anxiety Disorder 51 0.056
65
CCN001 Cocaine Dependence 49 0.056
66
HRT007 Heart Cancer 46 0.056
67
HPT020 Hepatic Vascular Disease 42 0.056
68
HMN016 Hemangioendothelioma 39 0.056
69
MSC004 Muscle Tissue Disease 34 0.056
70
P HRT017 Heart Tumor 32 0.056
71
P PHC003 Pheochromocytoma 71 0.051
72
MLN008 Melanoma 62 0.051
73
P NRV006 Nervous System Cancer 60 0.051
74
P TRM003 Tremor 54 0.051
75
SBS003 Substance Abuse 54 0.051
76
ANG020 Angiosarcoma 53 0.051
77
ATN002 Autonomic Nervous System Disease 48 0.051
78
RTN020 Retinal Vascular Disease 48 0.051
79
ALN001 Aland Island Eye Disease 45 0.051
80
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.051
81
PRD011 Proud Syndrome 42 0.051
82
KPS002 Kaposiform Hemangioendothelioma 41 0.051
83
ADJ001 Adjustment Disorder 38 0.051
84
c CNG031 Congenital Nervous System Abnormality 37 0.051
85
HRT029 Heart Tumor of the Child 15 0.051
86
P HPT023 Hepatocellular Carcinoma 92 0.046
87
P PRS040 Prostate Cancer 90 0.046
88
P AST005 Asthma 82 0.046
89
GST053 Gastric Cancer 78 0.046
90
P MDL005 Medulloblastoma 77 0.046
91
P NRB001 Neuroblastoma 70 0.046
92
TST021 Testicular Germ Cell Tumor 69 0.046
93
EWN003 Ewing Sarcoma 66 0.046
94
P ORT004 Orthostatic Intolerance 64 0.046
95
ATS001 Autistic Disorder 63 0.046
96
SKN019 Skin Melanoma 62 0.046
97
HYP056 Hypoglycemia 61 0.046
98
P PNC044 Pancreatitis 61 0.046
99
P PNC025 Panic Disorder 60 0.046
100
P PRP029 Porphyria 59 0.046
101
RSP006 Respiratory System Disease 58 0.046
102
P EXN002 Exanthem 57 0.046
103
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.046
104
NRN004 Neuroendocrine Tumor 56 0.046
105
CND002 Conduct Disorder 54 0.046
106
MNT002 Mental Depression 53 0.046
107
CRC006 Carcinoid Syndrome 52 0.046
108
CRN030 Coronary Stenosis 51 0.046
109
DRG003 Drug Dependence 50 0.046
110
LRN003 Learning Disability 49 0.046
111
OCL006 Ocular Hypertension 48 0.046
112
PLS009 Plasma Cell Neoplasm 48 0.046
113
NSD001 Nose Disease 48 0.046
114
P THY054 Thyrotoxic Periodic Paralysis 48 0.046
115
CCN002 Cocaine Abuse 48 0.046
116
SBS004 Substance Dependence 47 0.046
117
SYN036 Syncope 47 0.046
118
ACD009 Acid-Labile Subunit, Deficiency of 45 0.046
119
CHR008 Choroiditis 44 0.046
120
CRD118 Cardiovascular Cancer 44 0.046
121
SKN023 Skin Tag 44 0.046
122
PHY002 Physical Disorder 43 0.046
123
MLR006 Male Reproductive Organ Cancer 43 0.046
124
SPC010 Speech and Communication Disorders 41 0.046
125
CLV009 Clove Syndrome, Somatic 41 0.046
126
MYF002 Myofascial Pain Syndrome 39 0.046
127
WTH001 Withdrawal Disorder 37 0.046
128
GRM001 Germ Cell and Embryonal Cancer 36 0.046
129
NTR005 Nutritional Deficiency Disease 36 0.046
130
MLR007 Male Reproductive System Disease 34 0.046
131
c TRC078 Trichohepatoenteric Syndrome 2 29 0.046
132
c AST037 Asthma 1 28 0.046
133
c AST039 Asthma 2 28 0.046
134
PHC004 Phace Syndrome 27 0.046
135
NNT003 Neonatal Thyrotoxicosis 27 0.046
136
HYP029 Hyperthyroxinemia 26 0.046
137
c ADL096 Adult Hepatocellular Carcinoma 24 0.046
138
CMB002 Combat Disorder 21 0.046
139
c CRN177 Coronary Heart Disease 7 20 0.046
140
c CRN175 Coronary Heart Disease 4 19 0.046
141
c CRN172 Coronary Heart Disease 3 19 0.046
142
c CRN173 Coronary Heart Disease 8 18 0.046
143
P BRS047 Breast Cancer 100 0.040
144
P PNC035 Pancreatic Cancer 87 0.040
145
STR067 Stroke, Ischemic 75 0.040
146
WRN001 Werner Syndrome 67 0.040
147
P ATR011 Atrial Fibrillation 66 0.040
148
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.040
149
SRC014 Sarcoma 66 0.040
150
P ATS007 Autism Spectrum Disorder 65 0.040
151
CNT098 Central Core Disease 65 0.040
152
P ART023 Arthropathy 64 0.040
153
LNG099 Lung Disease 64 0.040
154
CRD119 Cardiac Arrest 61 0.040
155
MDD011 Mood Disorder 61 0.040
156
MLG108 Malignant Melanoma, Somatic 60 0.040
157
P ORL007 Oral Cavity Cancer 59 0.040
158
OCL009 Ocular Cancer 59 0.040
159
P ALC004 Alcohol Abuse 59 0.040
160
c FML001 Familial Atrial Fibrillation 58 0.040
161
ADR005 Adrenal Carcinoma 57 0.040
162
SFT003 Soft Tissue Sarcoma 57 0.040
163
ORL011 Oral Cancer 56 0.040
164
NRM005 Neuromuscular Disease 56 0.040
165
HPT019 Hepatic Encephalopathy 56 0.040
166
JNT002 Joint Disorders 55 0.040
167
P HYP076 Hyperthyroidism 55 0.040
168
LYM022 Lymphangioma 54 0.040
169
END040 Endogenous Depression 53 0.040
170
PRV006 Pervasive Developmental Disorder 53 0.040
171
RSC001 Rosacea 52 0.040
172
TRM010 Traumatic Brain Injury 52 0.040
173
PRT058 Pure Autonomic Failure 52 0.040
174
P MGR003 Migraine with Aura 52 0.040
175
BRN071 Brain Injury 52 0.040
176
PRS042 Prostate Disease 52 0.040
177
BRN038 Bronchial Disease 51 0.040
178
DRG011 Drug Addiction 51 0.040
179
SCK005 Sickle Cell Disease 51 0.040
180
SMT006 Somatoform Disorder 50 0.040
181
RTN023 Retinitis 50 0.040
182
P CHR345 Chronic Pain 50 0.040
183
OPT003 Opiate Dependence 50 0.040
184
CSY001 C Syndrome 50 0.040
185
ANG054 Angina Pectoris 50 0.040
186
BRX001 Bruxism 49 0.040
187
SRT004 Serotonin Syndrome 49 0.040
188
ATN005 Autonomic Dysfunction 49 0.040
189
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.040
190
LPD004 Lipoid Nephrosis 48 0.040
191
HPT014 Hepatorenal Syndrome 46 0.040
192
P SKN013 Skin Benign Neoplasm 43 0.040
193
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.040
194
HRT008 Heart Conduction Disease 42 0.040
195
SMT001 Somatization Disorder 42 0.040
196
P BLD051 Blood Coagulation Disease 42 0.040
197
VNT011 Ventricular Fibrillation, Familial, 1 41 0.040
198
HMT018 Hematopoietic Stem Cell Transplantation 41 0.040
199
WBR001 Weber Syndrome 41 0.040
200
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.040
201
MLN013 Melanoma Metastasis 40 0.040
202
P CNN004 Connective Tissue Cancer 40 0.040
203
ADT003 Auditory System Disease 40 0.040
204
c CLL012 Cell Type Benign Neoplasm 39 0.040
205
OCL010 Ocular Hypotension 38 0.040
206
MLG088 Malignant Germ Cell Tumor 38 0.040
207
c PRS116 Prostate Cancer 1 37 0.040
208
BLD054 Blood Protein Disease 37 0.040
209
P PRX010 Paroxysmal Ventricular Fibrillation 37 0.040
210
AMY002 Amyloid Tumor 37 0.040
211
BRS004 Breast Angiosarcoma 35 0.040
212
RDN001 Reading Disorder 34 0.040
213
FNT004 Fainting 33 0.040
214
c CNN010 Connective Tissue Benign Neoplasm 32 0.040
215
c MLN032 Melanoma, Cutaneous Malignant, 2 31 0.040
216
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.040
217
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.040
218
PDT004 Pediatric Angiosarcoma 24 0.040
219
BRS005 Breast Neuroendocrine Neoplasm 22 0.040
220
DFF022 Diffuse Neonatal Hemangiomatosis 21 0.040
221
c CHR344 Chronic Orthostatic Intolerance 18 0.040
222
c CRN176 Coronary Heart Disease 9 18 0.040
223
c ATS172 Autism 10 15 0.040
224
BRS054 Breast Hemangioma 14 0.040
225
MGR022 Migraine with or Without Aura 3 14 0.040
226
BLN008 Blind Hypotensive Eye 14 0.040
227
MLG008 Malignant Breast Melanoma 14 0.040
228
BRS040 Breast Capillary Hemangioma 9 0.040
229
P MLT019 Multiple Myeloma 83 0.032
230
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.032
231
P OVR042 Ovarian Cancer 76 0.032
232
ESP021 Esophageal Cancer 76 0.032
233
SCK003 Sickle Cell Anemia 71 0.032
234
P ADN016 Adenocarcinoma 69 0.032
235
P CRD011 Cardiomyopathy 68 0.032
236
OBS061 Obstructive Sleep Apnea 66 0.032
237
SKN016 Skin Disease 66 0.032
238
ATH003 Atherosclerosis 65 0.032
239
P THL005 Thalassemia 64 0.032
240
HMT002 Hematologic Cancer 64 0.032
241
DFC004 Deficiency Anemia 64 0.032
242
P HYP086 Hypothyroidism 64 0.032
243
P OST002 Osteoporosis 64 0.032
244
P INF037 Inflammatory Bowel Disease 63 0.032
245
ALC007 Alcohol Dependence 63 0.032
246
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.032
247
P HML002 Hemolytic Anemia 62 0.032
248
P CRN015 Cornelia De Lange Syndrome 62 0.032
249
GST092 Gastroesophageal Reflux 62 0.032
250
APH001 Aphthous Stomatitis 62 0.032
251
P SLP006 Sleep Apnea 61 0.032
252
ISC004 Ischemia 61 0.032
253
P TXP001 Toxoplasmosis 61 0.032
254
P LYM025 Lymphedema 61 0.032
255
VNW001 Von Willebrand's Disease 61 0.032
256
c SRC025 Sarcoidosis 1 61 0.032
257
BRS051 Breast Disease 61 0.032
258
c ACT075 Acute Myocardial Infarction 60 0.032
259
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.032
260
P GST049 Gastrointestinal System Cancer 60 0.032
261
LPM004 Lipoma 60 0.032
262
P DRR001 Diarrhea 60 0.032
263
ART021 Arteriosclerosis 58 0.032
264
RHM027 Rheumatic Disease 58 0.032
265
MLG056 Malignant Hyperthermia 58 0.032
266
P BRS044 Breast Adenocarcinoma 58 0.032
267
SCH014 Schistosomiasis 58 0.032
268
EMB004 Embryonal Carcinoma 57 0.032
269
RHB003 Rhabdomyosarcoma 57 0.032
270
THR024 Thrombosis 57 0.032
271
P HMR003 Hemorrhagic Disease 57 0.032
272
EXF001 Exfoliation Syndrome 57 0.032
273
c MCR115 Microvascular Complications of Diabetes 5 57 0.032
274
HYP266 Hypoxia 56 0.032
275
P LYM033 Lymphoproliferative Syndrome 56 0.032
276
P OVR049 Ovarian Disease 56 0.032
277
P FNC043 Fanconi Anemia, Complementation Group E 55 0.032
278
PLM012 Pulmonary Sarcoidosis 54 0.032
279
P THY032 Thyroiditis 54 0.032
280
P MCR129 Microvascular Complications of Diabetes 1 54 0.032
281
PST046 Post-Transplant Lymphoproliferative Disease 54 0.032
282
C3D001 C3 Deficiency 53 0.032
283
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.032
284
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.032
285
BLT006 Bilateral Breast Cancer 53 0.032
286
TLN003 Telangiectasis 52 0.032
287
GST040 Gastric Adenocarcinoma 52 0.032
288
HMG005 Hemoglobinopathy 52 0.032
289
P SPS003 Spastic Diplegia 52 0.032
290
LYM024 Lymphatic System Disease 52 0.032
291
c INF071 Inflammatory Bowel Disease 1 51 0.032
292
P HRD018 Hair Disease 51 0.032
293
IMM136 Immune System Disease 51 0.032
294
NDL013 Nodular Regenerative Hyperplasia 50 0.032
295
FML038 Female Reproductive Organ Cancer 50 0.032
296
FML037 Female Breast Cancer 50 0.032
297
c LYM107 Lymphoproliferative Syndrome 2 50 0.032
298
P CLL015 Collagen Disease 50 0.032
299
END035 Endocrine Gland Cancer 49 0.032
300
TRD006 Tardive Dyskinesia 49 0.032
301
RTN015 Retinal Cancer 49 0.032
302
MVM001 Movement Disease 49 0.032
303
ALC009 Alcoholic Liver Cirrhosis 49 0.032
304
BCL002 B Cell Deficiency 49 0.032
305
PRT018 Portal Vein Thrombosis 49 0.032
306
c CRN139 Cornelia De Lange Syndrome 1 48 0.032
307
RTN003 Retinal Ischemia 48 0.032
308
THY030 Thyroid Gland Disease 48 0.032
309
FML039 Female Reproductive System Disease 48 0.032
310
c CNG027 Congenital Hemolytic Anemia 48 0.032
311
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.032
312
HND002 Hand, Foot and Mouth Disease 47 0.032
313
c MLG069 Malignant Hypertension 47 0.032
314
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.032
315
BLD053 Blood Platelet Disease 46 0.032
316
c ACT078 Acute Porphyria 46 0.032
317
ICH054 Ichthyosis, X-Linked 46 0.032
318
DNT012 Dental Caries 46 0.032
319
SCL003 Social Phobia 46 0.032
320
HMN009 Hemangioblastoma 45 0.032
321
P PLN008 Peeling Skin Syndrome 45 0.032
322
ACR041 Acromelic Frontonasal Dysostosis 45 0.032
323
HDN002 Head Injury 45 0.032
324
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 0.032
325
VST004 Vestibular Disease 44 0.032
326
P DYS021 Dysautonomia 44 0.032
327
DBT008 Diabetic Angiopathy 44 0.032
328
c CNT015 Central Sleep Apnea 44 0.032
329
OVR094 Ovarian Epithelial Cancer 43 0.032
330
BRT030 Birth Defects 43 0.032
331
SKN027 Skin Conditions 43 0.032
332
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.032
333
LKC003 Leukocyte Disease 43 0.032
334
SNS023 Sensory System Cancer 43 0.032
335
c HRD007 Hereditary Lymphedema 42 0.032
336
DRR008 Diarrhea 1, Secretory Chloride, Congenital 42 0.032
337
CRD003 Cardiac Sarcoidosis 42 0.032
338
c LYM110 Lymphedema, Hereditary, Ia 41 0.032
339
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.032
340
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.032
341
PHC013 Phaeochromocytoma 41 0.032
342
RPR002 Reproductive System Disease 41 0.032
343
DCB001 Decubitus Ulcer 41 0.032
344
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.032
345
GRD001 Giardiasis 40 0.032
346
GST078 Gastrointestinal Allergy 40 0.032
347
c CHR096 Chronic Pulmonary Heart Disease 40 0.032
348
c PLN018 Peeling Skin Syndrome 2 40 0.032
349
c INF087 Inflammatory Bowel Disease 4 40 0.032
350
GND003 Gonadal Disease 39 0.032
351
P FML187 Familial Hypertension 38 0.032
352
ABR009 Abruzzo-Erickson Syndrome 38 0.032
353
SPC003 Specific Developmental Disorder 38 0.032
354
c CHR579 Chiari Malformation Type Ii 37 0.032
355
ANG037 Angiomatosis 37 0.032
356
OVR050 Ovarian Embryonal Carcinoma 36 0.032
357
PST055 Postural Hypotension 36 0.032
358
ATM014 Autoimmune Disease of Endocrine System 36 0.032
359
OVR104 Ovarian Melanoma 36 0.032
360
ALR002 Al-Raqad Syndrome 36 0.032
361
ATM012 Autoimmune Disease of Blood 35 0.032
362
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.032
363
PHB001 Phobic Disorder 34 0.032
364
c PLN017 Peeling Skin Syndrome 1 34 0.032
365
CSL001 Causalgia 34 0.032
366
IMP003 Impaired Renal Function Disease 34 0.032
367
ANG049 Angioedema Induced by Ace Inhibitors 34 0.032
368
c CNG439 Congenital Lymphedema 34 0.032
369
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.032
370
SKN006 Skin Sarcoidosis 33 0.032
371
c SRC023 Sarcoidosis 2 33 0.032
372
MRK002 Marek Disease 33 0.032
373
ADR040 Adrenal Gland Pheochromocytoma 33 0.032
374
DDN007 Duodenal Disease 33 0.032
375
DSS010 Dissociative Disorder 32 0.032
376
ENG004 Engraftment Syndrome 32 0.032
377
c BRS046 Breast Benign Neoplasm 32 0.032
378
PRS126 Prostate Cancer Susceptibility 32 0.032
379
c HMG004 Hemoglobin D Disease 31 0.032
380
CPM001 Cap Myopathy 30 0.032
381
VSC008 Vascular Hemostatic Disease 30 0.032
382
P SCK034 Sickle Beta Thalassemia 30 0.032
383
PDT040 Pediatric Hypertension 30 0.032
384
PRS044 Prostate Sarcoma 30 0.032
385
c MLN050 Melanoma, Cutaneous Malignant, 3 30 0.032
386
c PLN021 Peeling Skin Syndrome 3 29 0.032
387
c HMG029 Hemoglobin Se Disease 28 0.032
388
c NRB014 Neuroblastoma 3 28 0.032
389
BRS061 Breast Sarcoma 28 0.032
390
WRT002 Writing Disorder 27 0.032
391
BRS031 Breast Rhabdomyosarcoma 27 0.032
392
c CRN134 Cornelia De Lange Syndrome 2 27 0.032
393
PST048 Postural Orthostatic Tachycardia Syndrome 27 0.032
394
CNT023 Central Nervous System Hemangioma 26 0.032
395
c CRN135 Cornelia De Lange Syndrome 3 26 0.032
396
MLN064 Melanoma of Soft Tissue 26 0.032
397
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.032
398
c CNG478 Congenital Diarrhea 25 0.032
399
HMN012 Hemangioma of Lung 25 0.032
400
ATM052 Autoimmune Disease 1 25 0.032
401
OVR069 Ovarian Germ Cell Tumor 24 0.032
402
c MLN052 Melanoma, Cutaneous Malignant, 5 24 0.032
403
SBC016 Subacute Delirium 24 0.032
404
CNT017 Central Nervous System Origin Vertigo 24 0.032
405
MDR006 Moderate and Severe Traumatic Brain Injury 23 0.032
406
c INF093 Inflammatory Bowel Disease 14 23 0.032
407
DRG016 Drug Induced Dyskinesia 23 0.032
408
FCL001 Facial Dermatosis 23 0.032
409
SCK020 Sickle Cell - Hemoglobin D Disease 22 0.032
410
ISC009 Ischemic Retinopathy 21 0.032
411
c INF073 Inflammatory Bowel Disease 12 21 0.032
412
c INF079 Inflammatory Bowel Disease 20 21 0.032
413
P PRM145 Primary Anetoderma 20 0.032
414
P GNR027 Generalized Peeling Skin Syndrome 19 0.032
415
c INF074 Inflammatory Bowel Disease 15 19 0.032
416
DGS008 Digestive System Melanoma 17 0.032
417
PNL011 Pineal Region Germinoma 17 0.032
418
c NRB011 Neuroblastoma 4 17 0.032
419
c ADL079 Adult Heart Tumor 16 0.032
420
c SRC024 Sarcoidosis 3 16 0.032
421
c DYS033 Dysautonomia Like Disorder 16 0.032
422
ATM053 Autoimmune Disease 2 16 0.032
423
GLC077 Glucocorticoid Therapy, Response to 16 0.032
424
ATM055 Autoimmune Disease 4 15 0.032
425
AQG001 Aquagenic Pruritus 15 0.032
426
PRS005 Prostate Angiosarcoma 14 0.032
427
MGR023 Migraine Without Aura 4 14 0.032
428
GST005 Gastric Hemangioma 14 0.032
429
WSC001 Wisconsin Syndrome 14 0.032
430
MLG026 Male Genital Organ Vascular Disease 14 0.032
431
c FML303 Familial/multiple Cancer 14 0.032
432
c SPS018 Spastic Diplegia Infantile Type 13 0.032
433
BRS067 Breast Cancer, Childhood 12 0.032
434
c FML158 Familial Hemangioma 11 0.032
435
c SCK008 Sickle Delta Beta Thalassemia 9 0.032
436
HMN037 Hemangioma, Capillary Infantile Susceptibility 8 0.032
437
P CLR023 Colorectal Cancer 97 0.023
438
P OBS005 Obesity 92 0.023
439
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.023
440
P PLM037 Pulmonary Hypertension 79 0.023
441
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.023
442
P RTT002 Rett Syndrome 77 0.023
443
P SCH015 Schizophrenia 77 0.023
444
c DLT002 Dilated Cardiomyopathy 76 0.023
445
P ART022 Arthritis 75 0.023
446
END057 Endometrial Cancer 75 0.023
447
INS024 Insulin-Like Growth Factor I 75 0.023
448
P CRN211 Coronary Artery Disease 74 0.023
449
MRF001 Marfan Syndrome 73 0.023
450
c HPT073 Hepatitis C Virus 73 0.023
451
P INF038 Influenza 72 0.023
452
P PLM036 Pulmonary Fibrosis 71 0.023
453
P PRK057 Parkinson Disease, Late-Onset 70 0.023
454
BRN028 Brain Cancer 70 0.023
455
SQM006 Squamous Cell Carcinoma 70 0.023
456
c HPT001 Hepatitis C 68 0.023
457
ISC006 Ischemic Heart Disease 68 0.023
458
PCK002 Pick Disease 68 0.023
459
P PNM007 Pneumonia 68 0.023
460
P TBR001 Tuberous Sclerosis 67 0.023
461
VSC007 Vascular Disease 67 0.023
462
P MYS003 Myasthenia Gravis 67 0.023
463
P KDN018 Kidney Disease 66 0.023
464
c CHR089 Chronic Kidney Failure 66 0.023
465
P EPL164 Epilepsy 66 0.023
466
DRM006 Dermatitis 66 0.023
467
OBS002 Obsessive-Compulsive Disorder 66 0.023
468
DWN001 Down Syndrome 66 0.023
469
ATP002 Atopy 66 0.023
470
CRV047 Cervical Cancer, Somatic 65 0.023
471
P DYS154 Dystonia 65 0.023
472
P KDN017 Kidney Cancer 65 0.023
473
c HPT016 Hepatitis B 64 0.023
474
P LNG028 Long Qt Syndrome 64 0.023
475
CRB039 Cerebrovascular Disease 63 0.023
476
c TBR024 Tuberous Sclerosis-1 63 0.023
477
PRT036 Peritonitis 63 0.023
478
CNN005 Connective Tissue Disease 62 0.023
479
P PRS038 Personality Disorder 62 0.023
480
c LNG044 Long Qt Syndrome 1 62 0.023
481
CNT047 Contact Dermatitis 61 0.023
482
P PSR002 Psoriasis 61 0.023
483
P ESP024 Esophagitis 61 0.023
484
P HYP117 Hypertriglyceridemia 61 0.023
485
HYP066 Hyperglycemia 61 0.023
486
P DNT015 Dent Disease 61 0.023
487
P INT068 Intestinal Disease 60 0.023
488
FLL027 Fallopian Tube Carcinoma 60 0.023
489
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.023
490
P BRG001 Brugada Syndrome 59 0.023
491
KRT001 Keratoconjunctivitis Sicca 59 0.023
492
ALC006 Alcoholic Hepatitis 59 0.023
493
c HPT003 Hepatitis a 59 0.023
494
P GRV001 Graves' Disease 59 0.023
495
FTT001 Fatty Liver Disease 59 0.023
496
P NRP001 Neuropathy 59 0.023
497
P INF032 Infertility 59 0.023
498
WLL006 Wells Syndrome 59 0.023
499
LPD008 Lipid Metabolism Disorder 58 0.023
500
P SHR029 Short Syndrome 58 0.023
501
P GT001 Gout 58 0.023
502
P HYP060 Hyperinsulinism 58 0.023
503
P MSC007 Muscle Hypertrophy 58 0.023
504
CHL071 Child Syndrome 58 0.023
505
c LNG047 Long Qt Syndrome 2 57 0.023
506
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.023
507
ART017 Aortic Disease 57 0.023
508
c CWD006 Cowden Syndrome 1 57 0.023
509
CNS004 Constipation 57 0.023
510
ADM013 Adamantinoma of Long Bones 57 0.023
511
ALL010 Allergic Contact Dermatitis 57 0.023
512
WST001 West Syndrome 57 0.023
513
P SZR006 Seizure Disorder 56 0.023
514
P FBR017 Fibrosarcoma 56 0.023
515
CLR003 Clear Cell Adenocarcinoma 56 0.023
516
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.023
517
ART111 Artery Disease 55 0.023
518
PRP019 Peripheral Nervous System Disease 55 0.023
519
PLM034 Pulmonary Emphysema 55 0.023
520
GLC003 Glucose Intolerance 55 0.023
521
FCL014 Focal Epilepsy 55 0.023
522
PPL022 Papilloma 55 0.023
523
END030 End Stage Renal Failure 55 0.023
524
c THR092 Thrombophilia Due to Thrombin Defect 54 0.023
525
RCT018 Rectal Neoplasm 54 0.023
526
P MMB011 Membranous Nephropathy 54 0.023
527
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.023
528
c PRM126 Primary Peritoneal Carcinoma 54 0.023
529
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.023
530
P VNS003 Venous Insufficiency 54 0.023
531
RST001 Restless Legs Syndrome 54 0.023
532
CRV040 Cervix Carcinoma 53 0.023
533
DMY004 Demyelinating Disease 53 0.023
534
KDS001 Kid Syndrome 53 0.023
535
FDL002 Food Allergy 53 0.023
536
P LPC002 Lip Cancer 53 0.023
537
P EXP004 Exophthalmos 53 0.023
538
ZLL002 Zollinger-Ellison Syndrome 53 0.023
539
ADL002 Adult Syndrome 52 0.023
540
GTR002 Goiter 52 0.023
541
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.023
542
P ACT105 Acute Mountain Sickness 52 0.023
543
KRT006 Keratoconjunctivitis 52 0.023
544
P ANG015 Angioedema 52 0.023
545
c INF023 Inflammatory Breast Carcinoma 52 0.023
546
ALL026 Allergic Hypersensitivity Disease 52 0.023
547
OPT006 Optic Nerve Disease 52 0.023
548
c PRK031 Parkinson Disease 1 51 0.023
549
P ERY008 Erythromelalgia 51 0.023
550
TXC002 Toxic Encephalopathy 51 0.023
551
SRS001 Serous Cystadenocarcinoma 51 0.023
552
KLD001 Keloids 51 0.023
553
HYP005 Hypokalemia 51 0.023
554
CLN019 Colonic Disease 51 0.023
555
INT007 Intermediate Coronary Syndrome 50 0.023
556
MST017 Mast Cell Disease 50 0.023
557
MCN001 Mucinous Adenocarcinoma 50 0.023
558
P MSC003 Muscular Atrophy 50 0.023
559
NNL002 Nonalcoholic Steatohepatitis 50 0.023
560
URN009 Urinary System Disease 50 0.023
561
INT075 Intracranial Hypertension 50 0.023
562
P SCK002 Sick Sinus Syndrome 50 0.023
563
HYP006 Hypertensive Heart Disease 50 0.023
564
P URF003 Urofacial Syndrome 1 50 0.023
565
GLM004 Gliomatosis Cerebri 49 0.023
566
c ACT071 Acute Kidney Failure 49 0.023
567
PRN021 Paranasal Sinus Disease 49 0.023
568
c INF067 Inflammatory Bowel Disease 10 49 0.023
569
NCT008 Nicotine Dependence, Protection Against 49 0.023
570
c INH020 Inherited Metabolic Disorder 49 0.023
571
c LNG092 Long Qt Syndrome-3 49 0.023
572
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 48 0.023
573
BCT015 Bacteremia 48 0.023
574
MSS002 Mass Syndrome 48 0.023
575
CRN017 Coronary Thrombosis 48 0.023
576
c HMG001 Hemoglobin C Disease 47 0.023
577
CRN027 Corneal Neovascularization 47 0.023
578
RNL077 Renal Fibrosis 47 0.023
579
LYM116 Lymph Node Disease 47 0.023
580
INT253 Intestinal Benign Neoplasm 47 0.023
581
CRB027 Cerebellar Disease 47 0.023
582
SDD007 Sudden Cardiac Death 47 0.023
583
CYS014 Cystadenocarcinoma 47 0.023
584
BRD001 Brody Myopathy 47 0.023
585
DPM001 Dopamine Beta-Hydroxylase Deficiency 47 0.023
586
UPP004 Upper Respiratory Tract Disease 46 0.023
587
CRB085 Cerebral Hemorrhage 46 0.023
588
CRB025 Carbohydrate Metabolic Disorder 46 0.023
589
ART004 Aortic Atherosclerosis 46 0.023
590
ANG018 Angiomyolipoma 46 0.023
591
GLT021 Glutaricaciduria, Type I 46 0.023
592
P HRD021 Hereditary Sensory Neuropathy 46 0.023
593
P MRD002 Marden-Walker Syndrome 46 0.023
594
SPL012 Splenic Disease 46 0.023
595
ACH001 Acheiropody 46 0.023
596
LCT002 Lactose Intolerance 46 0.023
597
c MCR113 Microvascular Complications of Diabetes 3 45 0.023
598
SNS003 Sensory Peripheral Neuropathy 45 0.023
599
CRB004 Cerebral Artery Occlusion 45 0.023
600
P GNR032 Generalized Dystonia 45 0.023
601
P CRV039 Cervicitis 45 0.023
602
c CLR085 Colorectal Cancer 1 45 0.023
603
AST006 Astigmatism 45 0.023
604
ATN004 Autonomic Neuropathy 45 0.023
605
MXD023 Mixed Cell Type Cancer 44 0.023
606
c SHR030 Short Qt Syndrome 44 0.023
607
P OVR106 Ovarian Clear Cell Carcinoma 44 0.023
608
GDS001 Good Syndrome 44 0.023
609
P NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 44 0.023
610
OVR012 Ovarian Serous Cystadenocarcinoma 44 0.023
611
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 44 0.023
612
OCL069 Ocular Motor Apraxia 44 0.023
613
c GRV008 Graves Disease 1 44 0.023
614
c MTR002 Mitral Valve Insufficiency 44 0.023
615
CRN024 Corneal Disease 44 0.023
616
AGR002 Agoraphobia 44 0.023
617
c HMG003 Hemoglobin E Disease 44 0.023
618
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.023
619
EPT010 Epithelial-Myoepithelial Carcinoma 43 0.023
620
RNL097 Renal Artery Disease 43 0.023
621
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.023
622
HYP017 Hypophosphatemia 43 0.023
623
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.023
624
MST006 Mast Syndrome 43 0.023
625
PRD004 Prediabetes Syndrome 43 0.023
626
P CRD132 Cardiac Conduction Defect 43 0.023
627
CRB008 Cerebral Atherosclerosis 43 0.023
628
BHR001 Behr Syndrome 42 0.023
629
GLC008 Glucose Metabolism Disease 42 0.023
630
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.023
631
c NRP041 Neuropathy, Hereditary Sensory, Type Ie 42 0.023
632
ART008 Arteriosclerosis Obliterans 42 0.023
633
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.023
634
GST071 Gastrointestinal Carcinoma 42 0.023
635
RCR004 Recurrent Respiratory Papillomatosis 42 0.023
636
FCT008 Factitious Disorder 41 0.023
637
PRM025 Primary Bacterial Infectious Disease 41 0.023
638
PYG006 Pyogenic Granuloma 41 0.023
639
BRN080 Brain Ischemia 41 0.023
640
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.023
641
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 41 0.023
642
CNT060 Central Serous Chorioretinopathy 41 0.023
643
CHR413 Chronic Myocardial Ischemia 41 0.023
644
END038 Endocrine Pancreas Disease 41 0.023
645
KDN015 Kidney Angiomyolipoma 41 0.023
646
DMP001 Dumping Syndrome 40 0.023
647
CRN019 Coronary Artery Vasospasm 40 0.023
648
HRN003 Heroin Dependence 40 0.023
649
SQM002 Squamous Cell Papilloma 40 0.023
650
PSD029 Pseudocholinesterase Deficiency 40 0.023
651
RCT017 Rectal Disease 40 0.023
652
IMP006 Impulse Control Disorder 40 0.023
653
CNT099 Contractural Arachnodactyly, Congenital 40 0.023
654
c HRD088 Hereditary Neuropathies 40 0.023
655
BND014 Bone Development Disease 40 0.023
656
LYM020 Lymph Node Cancer 39 0.023
657
CRB009 Cerebritis 39 0.023
658
PRV003 Perivascular Epithelioid Cell Tumor 39 0.023
659
FLL023 Fallopian Tube Adenocarcinoma 39 0.023
660
LYM127 Lymphatic Malformations 39 0.023
661
MCN008 Mucinous Cystadenocarcinoma 39 0.023
662
OVR105 Ovarian Serous Carcinoma 39 0.023
663
PRN037 Prinzmetal's Variant Angina 39 0.023
664
ORB013 Orbital Disease 39 0.023
665
HYP540 Hypertension, Diastolic 39 0.023
666
PGM003 Pigmentation Disease 39 0.023
667
ADR009 Adrenal Cortex Disease 39 0.023
668
EYL005 Eyelid Disease 39 0.023
669
c INF086 Inflammatory Bowel Disease 3 38 0.023
670
NSL022 Nasal Cavity Disease 38 0.023
671
c PRK025 Parkinson Disease 10 38 0.023
672
INT025 Intermittent Explosive Disorder 38 0.023
673
APP009 Appendix Adenocarcinoma 38 0.023
674
c PRK030 Parkinson Disease 4 38 0.023
675
P HRT035 Heart Block, Congenital 38 0.023
676
P UTR038 Uterine Disease 37 0.023
677
BRN105 Burn Scar 37 0.023
678
PRP080 Peripheral Artery Disease 37 0.023
679
CYC008 Cyclic Vomiting Syndrome 37 0.023
680
VSC018 Visceral Steatosis 37 0.023
681
BNS002 Bone Structure Disease 37 0.023
682
P PST059 Pustular Psoriasis 36 0.023
683
MDY003 Mody, Type Ii 36 0.023
684
NSY001 N Syndrome 36 0.023
685
MLG098 Malignant Mixed Mullerian Tumor 36 0.023
686
OVR054 Ovarian Mucinous Neoplasm 36 0.023
687
OBS003 Obsessive-Compulsive Personality Disorder 36 0.023
688
OVR047 Ovarian Cystadenocarcinoma 36 0.023
689
OVR034 Ovarian Clear Cell Adenocarcinoma 36 0.023
690
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.023
691
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.023
692
GRV012 Grover's Disease 36 0.023
693
FCL011 Facial Nerve Disease 36 0.023
694
MYT011 Myotonia 36 0.023
695
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.023
696
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.023
697
CLR014 Clear Cell Adenoma 35 0.023
698
PRT035 Peritoneum Cancer 35 0.023
699
MYX004 Myxedema 35 0.023
700
CNT001 Contagious Pustular Dermatitis 34 0.023
701
IRT001 Iritis 34 0.023
702
MSN003 Mesenteric Vascular Occlusion 34 0.023
703
CRN021 Cornea Cancer 34 0.023
704
PLS010 Plasma Protein Metabolism Disease 34 0.023
705
CRD016 Cardiac Rupture 34 0.023
706
c INF089 Inflammatory Bowel Disease 6 34 0.023
707
ACR002 Acrocapitofemoral Dysplasia 33 0.023
708
c DGT005 Digital Arthropathy-Brachydactyly, Familial 33 0.023
709
P EPL003 Epulis 33 0.023
710
ACD004 Acdc 33 0.023
711
CHR010 Chorioangioma 33 0.023
712
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.023
713
c DNT021 Dent Disease 2 33 0.023
714
MTL005 Metal Allergy 33 0.023
715
FNC006 Functional Gastric Disease 32 0.023
716
CRV069 Cervix Disease 32 0.023
717
c CLR080 Colorectal Cancer 5 32 0.023
718
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 32 0.023
719
LYM095 Lymphangiomatosis 32 0.023
720
FLL029 Fallopian Tube Disease 32 0.023
721
c SNS009 Sensory Neuropathy Type 1 32 0.023
722
PHB003 Phobia, Specific 32 0.023
723
CVT001 Cavitary Optic Disc Anomalies 31 0.023
724
OVR013 Ovarian Mucinous Cystadenocarcinoma 31 0.023
725
c INF088 Inflammatory Bowel Disease 5 31 0.023
726
P ACT080 Acute Pulmonary Heart Disease 31 0.023
727
DRG004 Drug-Induced Mental Disorder 31 0.023
728
FST001 Foster-Kennedy Syndrome 31 0.023
729
c INF078 Inflammatory Bowel Disease 2 31 0.023
730
HNS001 Hansen's Disease 30 0.023
731
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.023
732
FLL003 Fallopian Tube Endometrioid Adenocarcinoma 30 0.023
733
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.023
734
END034 Endocrine Exophthalmos 29 0.023
735
c PRK026 Parkinson Disease 11 29 0.023
736
BRW006 Brown Syndrome 29 0.023
737
c DRR009 Diarrhea 6 29 0.023
738
GRN016 Grant Syndrome 29 0.023
739
C9D001 C9 Deficiency 29 0.023
740
c CLR079 Colorectal Cancer 2 29 0.023
741
c MLG080 Malignant Secondary Hypertension 28 0.023
742
c CLR075 Colorectal Cancer 3 28 0.023
743
SQM005 Squamous Papillomatosis 28 0.023
744
DBT081 Diabetic Encephalopathy 28 0.023
745
c NRB015 Neuroblastoma 2 28 0.023
746
DYS011 Dyskinesia of Esophagus 28 0.023
747
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.023
748
LPD027 Lip Disease 28 0.023
749
c MYC058 Myocardial Infarction 2 28 0.023
750
TYP027 Type 1 Diabetes Mellitus 10 27 0.023
751
CRB031 Cerebral Arterial Disease 27 0.023
752
c SHR033 Short Qt Syndrome 3 27 0.023
753
GNC005 Geniculate Ganglionitis 27 0.023
754
c SHR032 Short Qt Syndrome 2 27 0.023
755
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.023
756
c SHR031 Short Qt Syndrome 1 27 0.023
757
OVR011 Ovarian Mucinous Adenocarcinoma 26 0.023
758
CHR476 Chronic Angina 26 0.023
759
c NRP036 Neuropathy, Hereditary Sensory, Type if 26 0.023
760
c ATM089 Autoimmune Neuropathy 26 0.023
761
YNG002 Young Syndrome 26 0.023
762
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 26 0.023
763
END002 Endometrioid Ovary Carcinoma 25 0.023
764
PRM050 Primary Orthostatic Tremor 25 0.023
765
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.023
766
RSP004 Respiratory System Benign Neoplasm 25 0.023
767
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.023
768
P ATM050 Autoimmune Thyroid Disease 3 24 0.023
769
c MLT094 Multiple Sclerosis 3 24 0.023
770
c MJR007 Major Affective Disorder 1 24 0.023
771
EYC003 Eye Accommodation Disease 24 0.023
772
MCN018 Mucinous Adenocarcinoma of the Appendix 23 0.023
773
FCL064 Facial Dysmorphism with Multiple Malformations 23 0.023
774
PRT034 Peritoneal Serous Adenocarcinoma 23 0.023
775
HND001 Hand Dermatosis 23 0.023
776
ATR024 Atrial Fibrillation and Stroke 22 0.023
777
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.023
778
CRB087 Cerebral Arteriosclerosis 21 0.023
779
MND006 Mondor Disease 21 0.023
780
BNR002 Bone Resorption Disease 21 0.023
781
c PRK007 Parkinson Disease Type 3 21 0.023
782
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.023
783
RST012 Restless Legs Syndrome 1 20 0.023
784
c CRN174 Coronary Heart Disease 2 20 0.023
785
c RNL016 Renal Infectious Disease 20 0.023
786
c CHR464 Chronic Intestinal Failure 20 0.023
787
NLL002 Null Syndrome 20 0.023
788
c PRK008 Parkinson Disease Type 9 20 0.023
789
CYT018 Cytochrome P450 2d6 Variant 19 0.023
790
c MJR008 Major Affective Disorder 2 19 0.023
791
NNN007 Non-Involuting Congenital Hemangioma 19 0.023
792
ANM002 Animal Phobia 18 0.023
793
PRM227 Primary Orthostatic Hypotension 18 0.023
794
c MLT093 Multiple Sclerosis 2 18 0.023
795
c DYS137 Dystonia 4 18 0.023
796
ATN001 Autonomic Peripheral Neuropathy 17 0.023
797
RST014 Restless Legs Syndrome 3 17 0.023
798
FLY001 Flying Phobia 17 0.023
799
RPD005 Rapidly Involuting Congenital Hemangioma 17 0.023
800
BRB002 Barbiturate Dependence 16 0.023
801
c NRB013 Neuroblastoma 6 16 0.023
802
c ATS171 Autism 9 16 0.023
803
c FTT007 Fatty Liver Disease, Nonalcoholic 2 16 0.023
804
c MLT095 Multiple Sclerosis 4 16 0.023
805
c GRV009 Graves Disease 2 16 0.023
806
ATM054 Autoimmune Disease 3 15 0.023
807
c MJR006 Major Affective Disorder 5 15 0.023
808
ACT174 Acute Peripheral Arterial Occlusion 15 0.023
809
LPN002 Lip and Oral Cavity Cancer 15 0.023
810
c ATM057 Autoimmune Thyroid Disease 2 15 0.023
811
FLL022 Fallopian Tube Clear Cell Adenocarcinoma 15 0.023
812
RST015 Restless Legs Syndrome 4 14 0.023
813
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.023
814
CYP013 Cyp2c19-Related Poor Drug Metabolism 14 0.023
815
c ATM056 Autoimmune Thyroid Disease 1 14 0.023
816
c ATM058 Autoimmune Thyroid Disease 4 14 0.023
817
INT074 Intracranial Arteriosclerosis 14 0.023
818
P CYP006 Cyp2c19-Related Altered Drug Metabolism 14 0.023
819
c PNC070 Panic Disorder 2 14 0.023
820
MXD024 Mixed Epithelial Tumor of Ovary 13 0.023
821
MGR033 Migraine with or Without Aura 6 13 0.023
822
FLL002 Fallopian Tube Mucinous Tumor 12 0.023
823
BDS001 Bd Syndrome 12 0.023
824
FLL015 Fallopian Tube Serous Adenocarcinoma 12 0.023
825
FLL001 Fallopian Tube Mucinous Adenocarcinoma 11 0.023
826
OVR040 Ovarian Clear Cell Cystadenocarcinoma 11 0.023
827
c CYP009 Cyp2d6-Related Altered Drug Metabolism 11 0.023
828
HRD059 Hereditary Peripheral Nervous Disorder 11 0.023
829
HMT019 Hematohidrosis 10 0.023
830
CRN073 Coronary Arteries Congenital Malformation 10 0.023
831
CNG340 Congenital Anomaly of Hepatic Vein 10 0.023
832
c HRD063 Hereditary Type 2 Neuropathy 9 0.023
833
c HRD062 Hereditary Type 1 Neuropathy 9 0.023
834
HYP159 Hyperinsulinism, Focal 9 0.023
835
EPT002 Epithelioid Type Angiomyolipoma 8 0.023
Content
Loading form....