Search results for Propranolol

860 hits were found for Propranolol

# Family MCID Name MIFTS Score
1
P HMN010 Hemangioma 61 0.583
2
c HYP595 Hypertension, Essential 84 0.415
3
ANG054 Angina Pectoris 66 0.400
4
PRT013 Portal Hypertension 59 0.348
5
LVR012 Liver Cirrhosis 62 0.328
6
VRC005 Varicose Veins 60 0.316
7
c MGR028 Migraine with or Without Aura 1 67 0.314
8
HYP056 Hypoglycemia 66 0.277
9
P TRM003 Tremor 54 0.271
10
P HYP076 Hyperthyroidism 55 0.262
11
ESP002 Esophageal Varix 51 0.230
12
c GRV008 Graves Disease 1 56 0.220
13
RST023 Resting Heart Rate, Variation in 41 0.213
14
P MYC007 Myocardial Infarction 70 0.209
15
ANX010 Anxiety 73 0.205
16
c ESS001 Essential Tremor 56 0.201
17
c ACT075 Acute Myocardial Infarction 57 0.191
18
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.185
19
PST028 Post-Traumatic Stress Disorder 58 0.170
20
P CPL006 Capillary Hemangioma 51 0.167
21
ACT084 Acute Stress Disorder 47 0.165
22
CNG034 Congestive Heart Failure 69 0.158
23
P HDC001 Headache 57 0.158
24
P KDN018 Kidney Disease 72 0.148
25
c EXD008 Exudative Vitreoretinopathy 1 71 0.138
26
P HYP086 Hypothyroidism 69 0.134
27
LPP008 Lipoprotein Quantitative Trait Locus 62 0.134
28
c ATR087 Atrial Standstill 1 75 0.132
29
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.132
30
P CRN300 Coronary Heart Disease 1 63 0.130
31
DPR016 Depression 63 0.126
32
ALL026 Allergic Hypersensitivity Disease 62 0.126
33
P HRT032 Heart Disease 75 0.123
34
P ATR011 Atrial Fibrillation 66 0.121
35
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.121
36
P ORT004 Orthostatic Intolerance 62 0.121
37
P ENC018 Encephalopathy 61 0.117
38
HPT019 Hepatic Encephalopathy 60 0.117
39
HPT004 Hepatic Coma 45 0.117
40
P HYP061 Hypertrophic Cardiomyopathy 70 0.114
41
P LVR013 Liver Disease 68 0.114
42
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.114
43
TRD006 Tardive Dyskinesia 54 0.114
44
SYN036 Syncope 45 0.114
45
48X005 48,xyyy 39 0.114
46
ART140 Arteries, Anomalies of 52 0.112
47
TRM010 Traumatic Brain Injury 51 0.112
48
P MGR001 Migraine Without Aura 49 0.112
49
c ACT071 Acute Kidney Failure 60 0.109
50
INT007 Intermediate Coronary Syndrome 55 0.109
51
BRN071 Brain Injury 49 0.109
52
ISC004 Ischemia 58 0.107
53
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.104
54
ATR057 Atrioventricular Block 55 0.104
55
P GRV001 Graves' Disease 55 0.104
56
c CPL013 Capillary Malformations, Congenital 50 0.104
57
CHL079 Children's Interstitial Lung Disease 26 0.104
58
P PHC003 Pheochromocytoma 71 0.102
59
CRD132 Cardiac Conduction Defect 58 0.102
60
ADR040 Adrenal Gland Pheochromocytoma 46 0.102
61
AST005 Asthma 76 0.099
62
P SCH015 Schizophrenia 74 0.099
63
P TRN020 Turner Syndrome 67 0.099
64
MNT002 Mental Depression 58 0.099
65
HYP266 Hypoxia 57 0.099
66
OCL069 Ocular Motor Apraxia 51 0.099
67
WTH001 Withdrawal Disorder 48 0.099
68
HMN004 Hemangioma of Liver 36 0.099
69
P ATS364 Autism 70 0.096
70
P MLN008 Melanoma 69 0.096
71
P CRD119 Cardiac Arrest 67 0.096
72
PRT036 Peritonitis 64 0.096
73
c PNS012 Paine Syndrome 61 0.096
74
P RTN018 Retinal Disease 53 0.096
75
TLN003 Telangiectasis 52 0.096
76
PNG002 Pain Agnosia 51 0.096
77
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.096
78
PHC018 Phace Association 39 0.096
79
HMN016 Hemangioendothelioma 34 0.096
80
WLF001 Wolff-Parkinson-White Syndrome 66 0.093
81
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.093
82
SBG002 Subglottic Angioma 13 0.093
83
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.090
84
VSL002 Visual Epilepsy 59 0.090
85
P SZR006 Seizure Disorder 56 0.090
86
P PNC025 Panic Disorder 53 0.090
87
P TTR001 Tetralogy of Fallot 70 0.087
88
ADL002 Adult Syndrome 70 0.087
89
ANG020 Angiosarcoma 64 0.087
90
P VSC007 Vascular Disease 63 0.087
91
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.087
92
P PRP029 Porphyria 62 0.087
93
P EXN002 Exanthem 57 0.087
94
HYP005 Hypokalemia 55 0.087
95
AST006 Astigmatism 47 0.087
96
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.087
97
P HPT023 Hepatocellular Carcinoma 100 0.084
98
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.084
99
PRT058 Pure Autonomic Failure 59 0.084
100
SCH014 Schistosomiasis 57 0.084
101
P DRR001 Diarrhea 55 0.084
102
CRN030 Coronary Stenosis 50 0.084
103
AMB002 Amblyopia 49 0.084
104
P RNL015 Renal Hypertension 47 0.084
105
SPP007 Suppression Amblyopia 39 0.084
106
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.084
107
DFC004 Deficiency Anemia 70 0.081
108
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.081
109
SKN019 Skin Melanoma 68 0.081
110
c ATS007 Autism Spectrum Disorder 67 0.081
111
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.081
112
P PSR002 Psoriasis 62 0.081
113
P CRD246 Cardiovascular System Disease 57 0.081
114
PLM010 Pulmonary Edema 54 0.081
115
PST011 Pustulosis of Palm and Sole 52 0.081
116
PRT018 Portal Vein Thrombosis 50 0.081
117
HYP066 Hyperglycemia 61 0.077
118
AMN003 Amnestic Disorder 54 0.077
119
VSC006 Vascular Cancer 51 0.077
120
CCN002 Cocaine Abuse 49 0.077
121
BNR002 Bone Resorption Disease 48 0.077
122
CRD137 Cardiogenic Shock 47 0.077
123
SBV001 Subvalvular Aortic Stenosis 33 0.077
124
STR067 Stroke, Ischemic 81 0.074
125
P CRB048 Cerebral Cavernous Malformations 67 0.074
126
c RHB024 Rhabdomyosarcoma 2 67 0.074
127
ALC007 Alcohol Dependence 66 0.074
128
P DYS154 Dystonia 65 0.074
129
c FNC043 Fanconi Anemia, Complementation Group E 62 0.074
130
P HYP750 Hypertriglyceridemia, Familial 62 0.074
131
RTN017 Retinal Detachment 61 0.074
132
CRD223 Cardiac Arrhythmia 60 0.074
133
LYM022 Lymphangioma 54 0.074
134
NRT001 Neurotic Disorder 53 0.074
135
IMP005 Impotence 52 0.074
136
CCN001 Cocaine Dependence 48 0.074
137
KPS002 Kaposiform Hemangioendothelioma 43 0.074
138
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.074
139
P BRS047 Breast Cancer 97 0.070
140
P OST002 Osteoporosis 74 0.070
141
P LNG028 Long Qt Syndrome 66 0.070
142
TTN003 Tetanus 65 0.070
143
SRC014 Sarcoma 65 0.070
144
THR024 Thrombosis 57 0.070
145
P SCK002 Sick Sinus Syndrome 55 0.070
146
SPN035 Spindle Cell Sarcoma 53 0.070
147
P MTR003 Mitral Valve Stenosis 50 0.070
148
ATN005 Autonomic Dysfunction 46 0.070
149
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.070
150
P CHR345 Chronic Pain 44 0.070
151
ATX019 Ataxia with Vitamin E Deficiency 42 0.070
152
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.070
153
c CHR344 Chronic Orthostatic Intolerance 17 0.070
154
P PRS040 Prostate Cancer 97 0.066
155
P THR014 Thrombocytopenia 67 0.066
156
P PLM037 Pulmonary Hypertension 67 0.066
157
c FML001 Familial Atrial Fibrillation 65 0.066
158
LNG099 Lung Disease 60 0.066
159
INS001 Insulinoma 60 0.066
160
PPT005 Peptic Ulcer Disease 59 0.066
161
CNS004 Constipation 58 0.066
162
BRN038 Bronchial Disease 53 0.066
163
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.066
164
P PRD021 Periodic Paralysis 45 0.066
165
CYT002 Cytokine Deficiency 42 0.066
166
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.066
167
P DYS021 Dysautonomia 39 0.066
168
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.066
169
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.066
170
CVR010 Cavernous Malformation 30 0.066
171
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.062
172
c DLT002 Dilated Cardiomyopathy 79 0.062
173
MRF001 Marfan Syndrome 77 0.062
174
c HYP836 Hypercholesterolemia, Familial, 1 73 0.062
175
P NRB001 Neuroblastoma 72 0.062
176
PRP027 Peripheral Vascular Disease 71 0.062
177
c CHR684 Chronic Kidney Disease 70 0.062
178
CRB039 Cerebrovascular Disease 67 0.062
179
PSY004 Psychotic Disorder 67 0.062
180
ATH013 Atherosclerosis Susceptibility 65 0.062
181
PRP083 Porphyria, Acute Intermittent 64 0.062
182
P HYP069 Hyperparathyroidism 63 0.062
183
P MVM001 Movement Disease 63 0.062
184
ANR040 Aneurysm 59 0.062
185
DSS008 Disease of Mental Health 58 0.062
186
SFT003 Soft Tissue Sarcoma 56 0.062
187
GTR002 Goiter 53 0.062
188
P MGR003 Migraine with Aura 52 0.062
189
CVR006 Cavernous Hemangioma 49 0.062
190
P THY054 Thyrotoxic Periodic Paralysis 46 0.062
191
HDN002 Head Injury 46 0.062
192
SBC016 Subacute Delirium 44 0.062
193
BCK006 Back Pain 42 0.062
194
P MLG074 Malignant Mesenchymoma 40 0.062
195
NNT003 Neonatal Thyrotoxicosis 33 0.062
196
c PRS136 Prostate Cancer, Hereditary, 6 33 0.062
197
c PRS130 Prostate Cancer, Hereditary, 8 32 0.062
198
MYL069 Myeloma, Multiple 85 0.057
199
CRH001 Crohn's Disease 74 0.057
200
BRN024 Bronchitis 68 0.057
201
P MJR001 Major Depressive Disorder 68 0.057
202
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
203
c MCR129 Microvascular Complications of Diabetes 1 66 0.057
204
P HYD006 Hydrocephalus 66 0.057
205
P DBT009 Diabetes Mellitus 64 0.057
206
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.057
207
INT002 Intermittent Claudication 61 0.057
208
DRM006 Dermatitis 61 0.057
209
FBR047 Fibromyalgia 58 0.057
210
P PTS002 Ptosis 53 0.057
211
c FML191 Familial Long Qt Syndrome 53 0.057
212
EXP004 Exophthalmos 52 0.057
213
ACR041 Acromelic Frontonasal Dysostosis 52 0.057
214
P MSC003 Muscular Atrophy 52 0.057
215
SNT005 Sinoatrial Node Disease 49 0.057
216
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.057
217
STM006 Stomach Disease 47 0.057
218
P CRC039 Coarctation of Aorta 47 0.057
219
AGR002 Agoraphobia 45 0.057
220
MYF002 Myofascial Pain Syndrome 42 0.057
221
c MCR112 Microvascular Complications of Diabetes 2 41 0.057
222
ANX004 Anoxia 40 0.057
223
ANG065 Angioma, Tufted 38 0.057
224
THY001 Thyroid Crisis 31 0.057
225
FNT004 Fainting 30 0.057
226
P OVR042 Ovarian Cancer 88 0.052
227
P PNC035 Pancreatic Cancer 84 0.052
228
KPS004 Kaposi Sarcoma 75 0.052
229
P RSP003 Respiratory Failure 74 0.052
230
c THR092 Thrombophilia Due to Thrombin Defect 73 0.052
231
P MYP004 Myopathy 70 0.052
232
P SLP006 Sleep Apnea 69 0.052
233
PRP001 Propionic Acidemia 65 0.052
234
c DBT099 Diabetes Mellitus, Type I 65 0.052
235
P GLM045 Glioma 63 0.052
236
MDD011 Mood Disorder 62 0.052
237
P VNT002 Ventricular Septal Defect 60 0.052
238
P SLP005 Sleep Disorder 59 0.052
239
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.052
240
EYD002 Eye Disease 58 0.052
241
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.052
242
PPL022 Papilloma 54 0.052
243
ALC009 Alcoholic Liver Cirrhosis 53 0.052
244
ART074 Aortic Dissection 52 0.052
245
SKN013 Skin Benign Neoplasm 51 0.052
246
HPT014 Hepatorenal Syndrome 50 0.052
247
P SCK005 Sickle Cell Disease 50 0.052
248
RNL011 Renal Osteodystrophy 50 0.052
249
URM002 Uremia 49 0.052
250
SCL003 Social Phobia 48 0.052
251
c MCR120 Microvascular Complications of Diabetes 7 47 0.052
252
c CNG216 Congenital Hydrocephalus 47 0.052
253
GRW007 Growth Hormone Deficiency 46 0.052
254
GLL048 Glial Tumor 45 0.052
255
c PRM038 Primary Agammaglobulinemia 44 0.052
256
RFR003 Refractive Error 43 0.052
257
49X006 49, Xxxxy Syndrome 41 0.052
258
PYG006 Pyogenic Granuloma 41 0.052
259
HYP540 Hypertension, Diastolic 40 0.052
260
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.052
261
WBR001 Weber Syndrome 35 0.052
262
LYM095 Lymphangiomatosis 33 0.052
263
P RRL003 Rare Lymphatic Malformation 31 0.052
264
HYP645 Hyperthyroxinemia, Dystransthyretinemic 31 0.052
265
HYP029 Hyperthyroxinemia 31 0.052
266
VLK001 Volkmann Contracture 25 0.052
267
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.052
268
P CLR023 Colorectal Cancer 99 0.047
269
P GST053 Gastric Cancer 83 0.047
270
SCK003 Sickle Cell Anemia 74 0.047
271
VNH007 Von Hippel-Lindau Syndrome 73 0.047
272
P HNT016 Huntington Disease 72 0.047
273
P BRG001 Brugada Syndrome 71 0.047
274
ART016 Aortic Aneurysm 69 0.047
275
P HPT021 Hepatitis 67 0.047
276
P HYP098 Hypereosinophilic Syndrome 67 0.047
277
P SKN015 Skin Carcinoma 66 0.047
278
P NSP012 Nasopharyngeal Carcinoma 66 0.047
279
P ART005 Arteriovenous Malformation 65 0.047
280
P VNW001 Von Willebrand's Disease 65 0.047
281
PRT037 Pertussis 65 0.047
282
P PRS038 Personality Disorder 65 0.047
283
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.047
284
MSC007 Muscle Hypertrophy 64 0.047
285
P RHB003 Rhabdomyosarcoma 63 0.047
286
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.047
287
c PRC016 Pre-Eclampsia 63 0.047
288
c HPT001 Hepatitis C 62 0.047
289
P ART023 Arthropathy 62 0.047
290
HYD038 Hydrops Fetalis, Nonimmune 62 0.047
291
NTR005 Nutritional Deficiency Disease 62 0.047
292
FTT001 Fatty Liver Disease 61 0.047
293
P LPS004 Lupus Erythematosus 61 0.047
294
STR039 Sturge-Weber Syndrome 60 0.047
295
PRN019 Perinatal Necrotizing Enterocolitis 59 0.047
296
P ALC033 Alcohol Use Disorder 58 0.047
297
CNT047 Contact Dermatitis 58 0.047
298
IRN002 Iron Metabolism Disease 57 0.047
299
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.047
300
P PRV006 Pervasive Developmental Disorder 57 0.047
301
BLR008 Bilirubin Metabolic Disorder 57 0.047
302
P NRP001 Neuropathy 56 0.047
303
P MYP006 Myopia 55 0.047
304
P STR020 Strabismus 55 0.047
305
ACT058 Active Peptic Ulcer Disease 55 0.047
306
P SBS003 Substance Abuse 55 0.047
307
END040 Endogenous Depression 55 0.047
308
HYP060 Hyperinsulinism 54 0.047
309
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.047
310
P ALP008 Alopecia 54 0.047
311
OCL006 Ocular Hypertension 53 0.047
312
DNT012 Dental Caries 53 0.047
313
P DDN001 Duodenal Ulcer 52 0.047
314
P RCT021 Rectum Cancer 52 0.047
315
PLS009 Plasma Cell Neoplasm 51 0.047
316
ENT011 Enterocolitis 51 0.047
317
END086 End Stage Renal Disease 51 0.047
318
P OVR082 Overgrowth Syndrome 50 0.047
319
P ECL001 Eclampsia 50 0.047
320
c HRD202 Hereditary Lymphedema I 50 0.047
321
c INF145 Infantile Liver Failure Syndrome 1 50 0.047
322
MTB004 Metabolic Acidosis 50 0.047
323
47X002 47,xyy 49 0.047
324
P OPN001 Open-Angle Glaucoma 49 0.047
325
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.047
326
P RNV001 Renovascular Hypertension 48 0.047
327
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.047
328
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.047
329
CYN002 Cyanosis, Transient Neonatal 45 0.047
330
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.047
331
DMP001 Dumping Syndrome 44 0.047
332
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.047
333
MCH006 Mechanical Strabismus 42 0.047
334
RDN001 Reading Disorder 40 0.047
335
SPR126 Superior Semicircular Canal Dehiscence 40 0.047
336
ADJ001 Adjustment Disorder 40 0.047
337
c HMG029 Hemoglobin Se Disease 39 0.047
338
OVR094 Ovarian Epithelial Cancer 38 0.047
339
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.047
340
PRT112 Portal Hypertension, Noncirrhotic 31 0.047
341
TMP019 Temporomandibular Joint Anomaly 28 0.047
342
ANG037 Angiomatosis 28 0.047
343
DFF022 Diffuse Neonatal Hemangiomatosis 24 0.047
344
c SYS001 Systemic Lupus Erythematosus 86 0.040
346
c NRF023 Neurofibromatosis, Type Ii 80 0.040
347
CRV035 Cervical Cancer 76 0.040
348
BRN028 Brain Cancer 74 0.040
349
BSL036 Basal Cell Nevus Syndrome 73 0.040
350
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.040
351
GST040 Gastric Adenocarcinoma 70 0.040
352
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.040
353
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.040
354
CNN005 Connective Tissue Disease 68 0.040
355
GST092 Gastroesophageal Reflux 67 0.040
356
FLL027 Fallopian Tube Carcinoma 67 0.040
357
c LNG044 Long Qt Syndrome 1 66 0.040
358
P NRV007 Nervous System Disease 66 0.040
359
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.040
360
APN008 Apnea, Obstructive Sleep 64 0.040
361
GT001 Gout 64 0.040
362
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.040
363
P ADN016 Adenocarcinoma 64 0.040
364
SKN016 Skin Disease 63 0.040
365
INT146 Intervertebral Disc Disease 63 0.040
366
c ALP101 Alpha-Thalassemia 62 0.040
367
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.040
368
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.040
369
P PRM006 Primary Biliary Cirrhosis 62 0.040
370
P KDN017 Kidney Cancer 60 0.040
371
P TXP001 Toxoplasmosis 60 0.040
372
P PTN014 Patent Ductus Arteriosus 1 60 0.040
373
P THL005 Thalassemia 60 0.040
374
CHL014 Cholera 59 0.040
375
NWB001 Newborn Respiratory Distress Syndrome 58 0.040
376
P PLY018 Polycythemia 56 0.040
377
GST050 Gastrointestinal System Disease 56 0.040
378
P HYP024 Hypoparathyroidism 56 0.040
379
BRN004 Brain Edema 56 0.040
380
MRD002 Marden-Walker Syndrome 56 0.040
381
RSC001 Rosacea 54 0.040
382
HMN009 Hemangioblastoma 54 0.040
383
GLC003 Glucose Intolerance 54 0.040
384
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.040
385
PRC013 Pericarditis 54 0.040
386
P ART021 Arteriosclerosis 54 0.040
387
HMS001 Hemosiderosis 54 0.040
388
NNL006 Non-Alcoholic Steatohepatitis 54 0.040
389
HYP063 Hypersplenism 53 0.040
390
GST023 Gastric Ulcer 53 0.040
391
c PSR017 Psoriasis 2 53 0.040
392
P ATN002 Autonomic Nervous System Disease 52 0.040
393
c MCR113 Microvascular Complications of Diabetes 3 52 0.040
394
c VRL010 Viral Hepatitis 52 0.040
395
P NRC002 Narcolepsy 52 0.040
396
c PSR023 Psoriasis 1 52 0.040
397
c SCN007 Secondary Hyperparathyroidism 51 0.040
398
c HNT004 Huntington Disease-Like 2 50 0.040
399
BRX001 Bruxism 50 0.040
400
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.040
401
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.040
402
HRT011 Heart Septal Defect 50 0.040
403
HYP006 Hypertensive Heart Disease 49 0.040
404
GST049 Gastrointestinal System Cancer 49 0.040
405
P RCR004 Recurrent Respiratory Papillomatosis 49 0.040
406
P CMP008 Compartment Syndrome 49 0.040
407
SBS004 Substance Dependence 48 0.040
408
SPL018 Splenomegaly 48 0.040
409
DGN001 Degenerative Disc Disease 48 0.040
410
HYP025 Hyperphosphatemia 48 0.040
411
HLX001 Helix Syndrome 47 0.040
412
c PSR032 Psoriasis 11 47 0.040
413
GST071 Gastrointestinal Carcinoma 47 0.040
414
NDL013 Nodular Regenerative Hyperplasia 47 0.040
415
RYN005 Raynaud Phenomenon 47 0.040
416
PLY012 Polyhydramnios 46 0.040
417
CRN019 Coronary Artery Vasospasm 46 0.040
418
CNT017 Central Nervous System Origin Vertigo 45 0.040
419
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.040
420
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.040
421
GRN017 Granulocytopenia 44 0.040
422
SPN369 Spinal Disease 43 0.040
423
PLY068 Polysubstance Abuse 43 0.040
424
c PSR028 Psoriasis 7 42 0.040
425
c MCR130 Microvascular Complications of Diabetes 6 41 0.040
426
c MCR133 Microvascular Complications of Diabetes 4 41 0.040
427
c PSR018 Psoriasis 13 41 0.040
428
P RRH023 Rare Hereditary Hemochromatosis 41 0.040
429
RTR011 Retroperitoneal Fibrosis 40 0.040
430
PLC009 Placenta Praevia 39 0.040
431
c OVR114 Ovarian Cancer 1 38 0.040
432
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.040
433
c HNT011 Huntington Disease-Like 3 38 0.040
434
P PRM327 Primary Lymphedema 38 0.040
435
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.040
436
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.040
437
HRW001 Hair Whorl 36 0.040
438
CRY036 Cryptogenic Cirrhosis 36 0.040
439
MYT011 Myotonia 34 0.040
440
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.040
441
HST004 Histiocytoid Hemangioma 32 0.040
442
c BNG021 Benign Essential Hypertension 26 0.040
443
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.033
444
c TBR025 Tuberous Sclerosis 1 77 0.033
445
END057 Endometrial Cancer 74 0.033
446
SVR004 Severe Combined Immunodeficiency 73 0.033
447
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.033
448
MSC157 Muscular Dystrophy, Duchenne Type 72 0.033
449
c TBR026 Tuberous Sclerosis 2 72 0.033
450
c HPT073 Hepatitis C Virus 72 0.033
451
ACR007 Acromegaly 71 0.033
452
P EPL164 Epilepsy 71 0.033
453
P TBR001 Tuberous Sclerosis 70 0.033
454
P ART022 Arthritis 69 0.033
455
SVR097 Severe Cutaneous Adverse Reaction 69 0.033
456
P PNM007 Pneumonia 68 0.033
457
OBS002 Obsessive-Compulsive Disorder 68 0.033
458
GLL008 Gilles De La Tourette Syndrome 66 0.033
459
P DMN002 Dementia 66 0.033
460
P MSC005 Muscular Dystrophy 66 0.033
461
P HRP006 Herpes Simplex 65 0.033
462
LYS012 Lysosomal Acid Lipase Deficiency 65 0.033
463
TBC004 Tobacco Addiction 64 0.033
464
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.033
465
P HML002 Hemolytic Anemia 63 0.033
466
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.033
467
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.033
468
PRM126 Primary Peritoneal Carcinoma 62 0.033
469
TXC005 Toxic Shock Syndrome 62 0.033
470
CHL068 Cholestasis 61 0.033
471
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.033
472
ALC006 Alcoholic Hepatitis 61 0.033
473
HRP004 Herpes Zoster 60 0.033
474
P NPH012 Nephrotic Syndrome 60 0.033
475
P SCL018 Scoliosis 60 0.033
476
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.033
477
P OPT006 Optic Nerve Disease 60 0.033
478
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.033
479
IGR001 Ige Responsiveness, Atopic 59 0.033
480
BRN002 Bronchiolitis 59 0.033
481
GST045 Gastroenteritis 59 0.033
482
c PRM005 Primary Hyperparathyroidism 58 0.033
483
ERY003 Erythema Multiforme 58 0.033
484
P URT039 Urticaria 58 0.033
485
P RHN004 Rhinitis 57 0.033
486
DSS009 Disseminated Intravascular Coagulation 57 0.033
487
BRD001 Brody Myopathy 57 0.033
488
HMR039 Hemorrhage, Intracerebral 57 0.033
489
P ANG015 Angioedema 57 0.033
490
BCT022 Bacterial Infectious Disease 56 0.033
491
ALL010 Allergic Contact Dermatitis 56 0.033
492
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.033
493
c FML035 Familial Hyperlipidemia 55 0.033
494
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.033
495
P RST001 Restless Legs Syndrome 54 0.033
496
c LNG048 Long Qt Syndrome 3 53 0.033
497
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.033
498
STT041 Stuttering 52 0.033
499
THY030 Thyroid Gland Disease 52 0.033
500
HYP014 Hyperuricemia 52 0.033
501
SRS001 Serous Cystadenocarcinoma 52 0.033
502
SPS003 Spastic Diplegia 51 0.033
503
P SPP010 Suppressor of Tumorigenicity 3 51 0.033
504
ILS001 Ileus 51 0.033
505
P LCT001 Lactic Acidosis 51 0.033
506
CYS014 Cystadenocarcinoma 51 0.033
507
BHR001 Behr Syndrome 51 0.033
508
c ACT078 Acute Porphyria 51 0.033
509
c PYR010 Peyronie's Disease 50 0.033
510
CRT013 Carotid Stenosis 50 0.033
511
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.033
512
CLR003 Clear Cell Adenocarcinoma 50 0.033
513
OPT003 Opiate Dependence 50 0.033
514
HYP017 Hypophosphatemia 50 0.033
515
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.033
516
ISL003 Isolated Growth Hormone Deficiency 49 0.033
517
MCN001 Mucinous Adenocarcinoma 49 0.033
518
PLM041 Pulmonary Valve Stenosis 49 0.033
519
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 49 0.033
520
RGH001 Right Bundle Branch Block 48 0.033
521
c MTR002 Mitral Valve Insufficiency 48 0.033
522
OPD006 Opioid Addiction 48 0.033
523
ART004 Aortic Atherosclerosis 47 0.033
524
SXL003 Sexual Disorder 47 0.033
525
c MLG069 Malignant Hypertension 47 0.033
526
PRD004 Prediabetes Syndrome 47 0.033
527
KRT008 Keratopathy 47 0.033
528
CRN027 Corneal Neovascularization 47 0.033
529
P ERY008 Erythromelalgia 47 0.033
530
SRT004 Serotonin Syndrome 47 0.033
531
CYC008 Cyclic Vomiting Syndrome 47 0.033
532
P VTR007 Vitreoretinopathy 46 0.033
533
KRT013 Keratolytic Winter Erythema 46 0.033
534
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.033
535
P MYC033 Myoclonus 46 0.033
536
ANG018 Angiomyolipoma 46 0.033
537
SQM002 Squamous Cell Papilloma 46 0.033
538
c DRR009 Diarrhea 6 46 0.033
539
GRD001 Giardiasis 45 0.033
540
CSL001 Causalgia 45 0.033
541
APP009 Appendix Adenocarcinoma 44 0.033
542
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.033
543
CNN002 Cannabis Abuse 44 0.033
544
DWR001 Dwarfism 44 0.033
545
HRN003 Heroin Dependence 44 0.033
546
PRT035 Peritoneum Cancer 44 0.033
547
c ORT011 Orthostatic Hypotension 1 44 0.033
548
P CRN024 Corneal Disease 44 0.033
549
CRB090 Cerebral Hypoxia 44 0.033
550
DRG002 Drug-Induced Hepatitis 43 0.033
551
INT025 Intermittent Explosive Disorder 41 0.033
552
PHB003 Phobia, Specific 41 0.033
553
P RRT020 Rare Tumor 41 0.033
554
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.033
555
MCN008 Mucinous Cystadenocarcinoma 40 0.033
556
CNN001 Cannabis Dependence 40 0.033
557
ART008 Arteriosclerosis Obliterans 40 0.033
558
CRB086 Cerebral Aneurysms 40 0.033
559
HYP344 Hyperthyroidism, Familial Gestational 39 0.033
560
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.033
561
ALL014 Allergic Encephalomyelitis 38 0.033
562
CNT060 Central Serous Chorioretinopathy 38 0.033
563
c TRM024 Tremor, Hereditary Essential, 1 37 0.033
564
ANS004 Anisometropia 35 0.033
565
SCN049 Second-Degree Atrioventricular Block 35 0.033
566
c MYC058 Myocardial Infarction 2 34 0.033
567
P VSC018 Visceral Steatosis 33 0.033
568
DYS198 Dystonia, Focal, Task-Specific 32 0.033
569
LYM035 Lymphangiectasis 30 0.033
570
ERY066 Erythema Multiforme Major 30 0.033
571
PST092 Posttransplant Acute Limbic Encephalitis 29 0.033
572
FLL022 Fallopian Tube Clear Cell Adenocarcinoma 28 0.033
573
CHR010 Chorioangioma 27 0.033
574
PRQ002 Paraquat Poisoning 26 0.033
575
FTL073 Fetal Anticonvulsant Syndrome 26 0.033
576
P PRX010 Paroxysmal Ventricular Fibrillation 25 0.033
577
STR029 Sternal Cleft 25 0.033
578
ATR089 Atrioventricular Dissociation 20 0.033
579
AQG001 Aquagenic Pruritus 19 0.033
580
HMT019 Hematohidrosis 15 0.033
581
LRY034 Laryngotracheal Angioma 13 0.033
582
PRT124 Portal Vein, Cavernous Transformation of 11 0.033
583
P ALZ034 Alzheimer Disease 88 0.023
584
P ATX030 Ataxia-Telangiectasia 82 0.023
585
P RTT002 Rett Syndrome 80 0.023
586
P RHM011 Rheumatoid Arthritis 80 0.023
587
INS024 Insulin-Like Growth Factor I 79 0.023
588
OST012 Osteoarthritis 78 0.023
589
P LNG064 Lung Cancer Susceptibility 3 78 0.023
590
P PRK057 Parkinson Disease, Late-Onset 78 0.023
591
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.023
592
P NNN008 Noonan Syndrome 1 76 0.023
593
GLB015 Glioblastoma Multiforme 75 0.023
594
P APL001 Aplastic Anemia 74 0.023
595
P MLT020 Multiple Sclerosis 72 0.023
596
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.023
597
P GRF003 Graft-Versus-Host Disease 72 0.023
598
P SRC025 Sarcoidosis 1 70 0.023
599
DWN001 Down Syndrome 70 0.023
600
c GLY008 Glycogen Storage Disease Ii 70 0.023
601
P FRG001 Fragile X Syndrome 70 0.023
602
PLM001 Pulmonary Tuberculosis 69 0.023
603
P LPR021 Leprosy 3 69 0.023
604
P LKM002 Leukemia 68 0.023
605
P MYS003 Myasthenia Gravis 68 0.023
606
ALL003 Allergic Rhinitis 67 0.023
607
CRP001 Carpal Tunnel Syndrome 67 0.023
608
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.023
609
P MLG056 Malignant Hyperthermia 67 0.023
610
OST159 Osteogenic Sarcoma 66 0.023
611
CHG001 Chagas Disease 66 0.023
612
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.023
613
P LPS002 Liposarcoma 65 0.023
614
IRR002 Irritable Bowel Syndrome 65 0.023
615
P CTS001 Cutis Laxa 65 0.023
616
P ADL010 Adult Respiratory Distress Syndrome 65 0.023
617
CLN015 Colon Adenocarcinoma 65 0.023
618
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.023
619
NRF007 Neurofibroma 64 0.023
620
P MST009 Mastocytosis 64 0.023
621
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.023
622
TRN015 Transient Cerebral Ischemia 63 0.023
623
P END044 Endometriosis 63 0.023
624
c ATM011 Autoimmune Hepatitis 63 0.023
625
c GLC092 Glaucoma, Primary Open Angle 62 0.023
626
LPD008 Lipid Metabolism Disorder 62 0.023
627
c BRN108 Branchiootic Syndrome 1 62 0.023
628
c SVR001 Severe Acute Respiratory Syndrome 62 0.023
629
P VSC011 Vasculitis 62 0.023
630
c SCL052 Scleroderma, Familial Progressive 61 0.023
631
P ENC004 Encephalitis 61 0.023
632
CHR066 Chronic Fatigue Syndrome 61 0.023
633
DCB001 Decubitus Ulcer 61 0.023
634
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.023
635
P MYL006 Myeloid Leukemia 60 0.023
636
INT066 Interstitial Lung Disease 60 0.023
637
c ACT027 Acute Pancreatitis 60 0.023
638
P ALP009 Alopecia Areata 60 0.023
639
SQM006 Squamous Cell Carcinoma 60 0.023
640
P ATR010 Atrial Heart Septal Defect 60 0.023
641
P SNS001 Sensorineural Hearing Loss 60 0.023
642
P CTR002 Cataract 60 0.023
643
ETN001 Eating Disorder 60 0.023
644
P MYC008 Myocarditis 59 0.023
645
P BND020 Bone Disease 59 0.023
646
c HPT016 Hepatitis B 59 0.023
647
THY029 Thyroid Carcinoma 59 0.023
648
PLM033 Pulmonary Embolism 59 0.023
649
P BRS044 Breast Adenocarcinoma 59 0.023
650
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.023
651
IRN001 Iron Deficiency Anemia 59 0.023
652
ADN018 Adenoma 59 0.023
653
c LNG047 Long Qt Syndrome 2 58 0.023
654
P BCL017 B-Cell Lymphoma 58 0.023
655
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.023
656
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.023
657
EXT034 Extrinsic Allergic Alveolitis 58 0.023
658
c CHL119 Cholangitis, Primary Sclerosing 57 0.023
659
APH002 Aphasia 57 0.023
660
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.023
661
PLC005 Placental Insufficiency 57 0.023
662
CMR002 Coumarin Resistance 56 0.023
663
P FBR017 Fibrosarcoma 56 0.023
664
P PLY011 Polycystic Ovary Syndrome 56 0.023
665
P MLT074 Multiple Endocrine Neoplasia 56 0.023
666
PLS011 Plasmacytoma 56 0.023
667
P MTC069 Mitochondrial Disorders 56 0.023
668
GNR004 Generalized Anxiety Disorder 56 0.023
669
VRG001 Variegate Porphyria 56 0.023
670
P TMR010 Tumor Predisposition Syndrome 56 0.023
671
OVR012 Ovarian Serous Cystadenocarcinoma 56 0.023
672
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.023
673
P NRF002 Neurofibromatosis 56 0.023
674
INT030 Intracranial Aneurysm 56 0.023
675
P MYT023 Myotonia Congenita 56 0.023
676
AGN016 Aging 56 0.023
677
MCL006 Macular Retinal Edema 55 0.023
678
ZLL002 Zollinger-Ellison Syndrome 55 0.023
679
P PLM034 Pulmonary Emphysema 55 0.023
680
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.023
681
CHR100 Chronic Ulcer of Skin 55 0.023
682
CRC006 Carcinoid Syndrome 55 0.023
683
P DBT005 Diabetes Insipidus 55 0.023
684
RFL001 Reflex Sympathetic Dystrophy 54 0.023
685
AMN001 Amenorrhea 54 0.023
686
P TCD001 Tic Disorder 53 0.023
687
P EPD016 Epidermolysis Bullosa 53 0.023
688
KRT006 Keratoconjunctivitis 53 0.023
689
P HML001 Hemolytic-Uremic Syndrome 53 0.023
690
ACR058 Acrofacial Dysostosis 1, Nager Type 53 0.023
691
INT075 Intracranial Hypertension 53 0.023
692
IRD001 Iridocyclitis 53 0.023
693
P PRG013 Paraganglioma 52 0.023
694
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.023
695
P ACT105 Acute Mountain Sickness 52 0.023
696
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.023
697
LMY002 Leiomyoma 52 0.023
699
NRM004 Neuroma 51 0.023
700
P PRC012 Pericardial Effusion 51 0.023
701
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.023
702
P CHL066 Cholangitis 51 0.023
703
HYP081 Hypolipoproteinemia 51 0.023
704
P HYP077 Hypertrichosis 50 0.023
705
RTN003 Retinal Ischemia 50 0.023
706
STT002 Status Asthmaticus 50 0.023
707
NTR046 Neutrophil Migration 50 0.023
708
LPR001 Lepromatous Leprosy 50 0.023
709
c PSR021 Psoriasis 14, Pustular 50 0.023
710
KRT001 Keratoconjunctivitis Sicca 49 0.023
711
P ART018 Aortic Valve Insufficiency 49 0.023
712
LFT001 Left Bundle Branch Hemiblock 49 0.023
713
c BPL002 Bipolar I Disorder 49 0.023
714
EPD006 Epidermolysis Bullosa Acquisita 49 0.023
715
LRN003 Learning Disability 49 0.023
716
QDR001 Quadriplegia 48 0.023
717
HYP043 Hyperandrogenism 48 0.023
718
c ACT150 Acute Adrenal Insufficiency 48 0.023
719
P SCL009 Sclerosing Cholangitis 48 0.023
720
INT067 Interstitial Nephritis 48 0.023
721
HMP001 Hemopericardium 48 0.023
722
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.023
723
MLT006 Multidrug-Resistant Tuberculosis 48 0.023
724
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.023
725
DRG003 Drug Dependence 47 0.023
726
CRD001 Cardiac Tamponade 47 0.023
727
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 0.023
728
HYP016 Hypochondriasis 47 0.023
729
NDL007 Nodular Goiter 47 0.023
730
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.023
731
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.023
732
P JVN008 Juvenile Glaucoma 47 0.023
733
MDS022 Mediastinitis 46 0.023
734
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.023
735
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.023
736
FCL012 Facial Paralysis 46 0.023
737
PLL012 Pollen Allergy 46 0.023
738
OBS003 Obsessive-Compulsive Personality Disorder 46 0.023
739
BNS007 Bone Sarcoma 45 0.023
740
GST030 Gastrinoma 45 0.023
741
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.023
742
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.023
743
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.023
744
IMM003 Immunoglobulin Alpha Deficiency 45 0.023
745
PRL008 Paralytic Ileus 45 0.023
746
ACT003 Acute Kidney Tubular Necrosis 45 0.023
747
CYS009 Cystadenoma 44 0.023
748
PTT037 Pituitary Tumors 44 0.023
749
IRT001 Iritis 44 0.023
750
CRB008 Cerebral Atherosclerosis 44 0.023
751
PRM003 Premature Ejaculation 44 0.023
752
CRP002 Croup 44 0.023
753
c FML036 Familial Periodic Paralysis 44 0.023
754
DYS018 Dysostosis 44 0.023
755
c SPR086 Spermatogenic Failure 3 44 0.023
756
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.023
757
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.023
758
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.023
759
MYX004 Myxedema 43 0.023
760
HYP457 Hypertrophic Scars 42 0.023
761
c RTN047 Retinitis Pigmentosa 18 42 0.023
762
GLM008 Glomus Tumor 42 0.023
763
P CLS010 Cluster Headache 42 0.023
764
ALC010 Alcoholic Cardiomyopathy 42 0.023
765
DRG024 Drug Allergy 42 0.023
766
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.023
767
P HYP087 Hypotrichosis 42 0.023
768
OCL052 Ocular Dominance 42 0.023
769
PHB001 Phobic Disorder 41 0.023
770
GST020 Gastric Antral Vascular Ectasia 41 0.023
771
PRK003 Parkes Weber Syndrome 41 0.023
772
PRS063 Paresthesia 41 0.023
773
VST004 Vestibular Disease 41 0.023
774
WLL039 Well-Differentiated Liposarcoma 41 0.023
775
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.023
776
ANG049 Angioedema Induced by Ace Inhibitors 40 0.023
777
PLY100 Polyploidy 40 0.023
778
C1N001 C1 Inhibitor Deficiency 39 0.023
779
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 39 0.023
780
HYP008 Hypertensive Retinopathy 39 0.023
781
ALG001 Algoneurodystrophy 39 0.023
782
c 46X079 46,xy Sex Reversal 11 39 0.023
783
c CHR682 Chronic Bilirubin Encephalopathy 39 0.023
784
P PRC031 Preeclampsia/eclampsia 1 38 0.023
785
c PLY105 Polycystic Ovary Syndrome 1 38 0.023
786
THY069 Thyroid Hormone Resistance, Selective Pituitary 38 0.023
787
CHY005 Chylothorax, Congenital 38 0.023
788
NMN001 Nominal Aphasia 38 0.023
789
P PST059 Pustular Psoriasis 37 0.023
790
PRV003 Perivascular Epithelioid Cell Tumor 37 0.023
791
GLM044 Glomerular Disease 37 0.023
792
HYP026 Hypoglycemic Coma 36 0.023
793
P HYP120 Hypoaldosteronism 36 0.023
794
HYP007 Hypermobility Syndrome 36 0.023
795
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.023
796
CRB159 Cerebral Visual Impairment 35 0.023
797
FXD003 Fixed Drug Eruption 35 0.023
798
BRK012 Broken Heart Syndrome 35 0.023
799
CHR178 Chromosomal Triplication 35 0.023
800
c THY084 Thyrotoxic Periodic Paralysis 1 35 0.023
801
CHR034 Chromophobe Adenoma 34 0.023
802
HNS001 Hansen's Disease 34 0.023
803
NNT039 Neonatal Marfan Syndrome 34 0.023
805
c RST012 Restless Legs Syndrome 1 34 0.023
806
PPL052 Papillomatosis, Confluent and Reticulated 33 0.023
807
RTC003 Root Caries 33 0.023
808
GRN009 Granulomatous Hepatitis 33 0.023
809
MCR119 Microtia, Hearing Impairment, and Cleft Palate 33 0.023
810
NNN007 Non-Involuting Congenital Hemangioma 33 0.023
811
EXN001 Exanthema Subitum 32 0.023
812
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.023
813
ACR017 Acrofacial Dysostosis 31 0.023
814
c THY083 Thyrotoxic Periodic Paralysis 2 31 0.023
815
SPS016 Spasmodic Dysphonia 31 0.023
816
c PRM158 Primary Intestinal Lymphangiectasia 31 0.023
817
CHL035 Cholinergic Urticaria 30 0.023
818
P EPL003 Epulis 30 0.023
819
BRT055 Breath-Holding Spells 30 0.023
820
CYS041 Cystic Angiomatosis of Bone, Diffuse 28 0.023
821
RTN013 Retinal Hemangioblastoma 28 0.023
822
GNT005 Giant Hemangioma 28 0.023
823
P MYS047 Myasthenic Syndrome, Congenital, 1b, Fast-Channel 28 0.023
824
c CRD083 Cardiomyopathy, Familial Hypertrophic, 15 28 0.023
825
CCN009 Cocaine Intoxication 27 0.023
826
FCL007 Facial Neuralgia 27 0.023
827
CYT018 Cytochrome P450 2d6 Variant 27 0.023
828
EXF003 Exfoliative Dermatitis 27 0.023
829
BRB002 Barbiturate Dependence 27 0.023
830
BNG077 Benign Idiopathic Neonatal Seizures 26 0.023
831
c CRB051 Cerebral Cavernous Malformation, Familial 26 0.023
832
GST005 Gastric Hemangioma 26 0.023
833
HMN008 Hemangioma of Subcutaneous Tissue 25 0.023
834
PNC018 Pancreatic Serous Cystadenoma 24 0.023
835
ACC002 Accommodative Spasm 24 0.023
836
ANT078 Antipyrine Metabolism 24 0.023
837
MSC193 Muscular Lipidosis 23 0.023
838
INT074 Intracranial Arteriosclerosis 23 0.023
839
HMN012 Hemangioma of Lung 23 0.023
840
ABR001 Aberrant Subclavian Artery 22 0.023
841
SBN001 Subendocardial Myocardial Infarction 22 0.023
842
URM001 Uremic Neuropathy 22 0.023
843
CRN309 Cranial Neuralgia 22 0.023
844
LPD042 Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency 21 0.023
846
NWD001 New Daily-Persistent Headache 21 0.023
847
c PSD047 Pseudo-Turner Syndrome 21 0.023
848
BNT001 Banti's Syndrome 21 0.023
849
MRF007 Marfanoid Hypermobility Syndrome 21 0.023
850
MLT146 Multicore Myopathy with Mental Retardation, Short Stature, and Hypogonadotropic Hypogonadism 20 0.023
851
RRV005 Rare Vascular Tumor 20 0.023
852
c CRN174 Coronary Heart Disease 2 19 0.023
853
BDR001 Bidirectional Tachycardia 19 0.023
854
MYP026 Myopathy - Thyrotoxic 17 0.023
855
c FML159 Familial Periodic Paralyses 16 0.023
856
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 16 0.023
857
ORG003 Organic Mood Syndrome 14 0.023
858
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 14 0.023
859
P CRB180 Cerebelloparenchymal Disorder Ii 13 0.023
860
BNG011 Benign Shuddering Attacks 7 0.023
Content
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