Search results for Propranolol

413 hits were found for Propranolol

# Family MCID Name MIFTS Score
1
P HMN010 Hemangioma 61 0.313
2
PSY004 Psychotic Disorder 72 0.217
3
P LVR013 Liver Disease 76 0.205
4
ANX010 Anxiety 72 0.195
5
LVR012 Liver Cirrhosis 73 0.193
6
PST028 Post-Traumatic Stress Disorder 59 0.185
7
GST050 Gastrointestinal System Disease 66 0.182
8
P PRT013 Portal Hypertension 59 0.180
9
VRC005 Varicose Veins 64 0.177
10
P NRV007 Nervous System Disease 75 0.174
11
P CPL006 Capillary Hemangioma 56 0.171
12
ESP002 Esophageal Varix 46 0.171
13
P ENC018 Encephalopathy 58 0.159
14
c CNT035 Central Nervous System Disease 65 0.153
15
BRN106 Burns 57 0.147
16
MNT002 Mental Depression 60 0.143
17
ESP023 Esophageal Disease 58 0.140
18
P HRT032 Heart Disease 80 0.136
19
PLC008 Placenta Disease 48 0.136
20
c EXD008 Exudative Vitreoretinopathy 1 65 0.133
21
P ORT004 Orthostatic Intolerance 68 0.129
22
RTN018 Retinal Disease 56 0.129
23
HDC001 Headache 55 0.129
24
CPL013 Capillary Malformations, Congenital 39 0.129
25
STR005 Stork Bite 15 0.129
26
ATN002 Autonomic Nervous System Disease 51 0.125
27
ATN005 Autonomic Dysfunction 51 0.125
28
P DYS021 Dysautonomia 47 0.125
29
AST005 Asthma 83 0.117
30
CCN001 Cocaine Dependence 52 0.113
31
ACT058 Active Peptic Ulcer Disease 43 0.113
32
P BRS047 Breast Cancer 100 0.108
33
MLN008 Melanoma 72 0.108
34
VSC007 Vascular Disease 71 0.108
35
SKN019 Skin Melanoma 63 0.108
36
END072 Endotheliitis 46 0.108
37
PNG002 Pain Agnosia 41 0.108
38
P HPT021 Hepatitis 75 0.104
39
PST048 Postural Orthostatic Tachycardia Syndrome 31 0.104
40
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.104
41
P HPT023 Hepatocellular Carcinoma 94 0.099
42
P ADN016 Adenocarcinoma 71 0.099
43
c ESS001 Essential Tremor 58 0.099
44
NRN004 Neuroendocrine Tumor 58 0.099
45
EWN002 Ewing's Family of Tumors 49 0.099
46
P MYC007 Myocardial Infarction 81 0.094
47
RTN017 Retinal Detachment 59 0.094
48
BRN071 Brain Injury 54 0.094
49
MGR001 Migraine Without Aura 47 0.094
50
c CHR344 Chronic Orthostatic Intolerance 18 0.094
51
CNG034 Congestive Heart Failure 74 0.088
52
P MYP004 Myopathy 69 0.088
53
LNG099 Lung Disease 67 0.088
54
RSP006 Respiratory System Disease 63 0.088
55
HYP056 Hypoglycemia 62 0.088
56
HPT019 Hepatic Encephalopathy 59 0.088
57
ANG020 Angiosarcoma 57 0.088
58
TRM010 Traumatic Brain Injury 54 0.088
59
P TRM003 Tremor 54 0.088
60
MSC033 Muscle Disorders 53 0.088
61
HDN002 Head Injury 48 0.088
62
MSC004 Muscle Tissue Disease 39 0.088
63
P ATS364 Autism 70 0.083
64
P EXN002 Exanthem 62 0.083
65
SLP005 Sleep Disorder 59 0.083
66
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.083
67
c PNS012 Paine Syndrome 52 0.083
68
P RNL015 Renal Hypertension 46 0.083
69
MYF002 Myofascial Pain Syndrome 44 0.083
70
MVM001 Movement Disease 40 0.083
71
c TRC078 Trichohepatoenteric Syndrome 2 34 0.083
72
P PRS040 Prostate Cancer 88 0.077
73
c HYP595 Hypertension, Essential 78 0.077
74
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.077
75
P DBT009 Diabetes Mellitus 72 0.077
76
P KDN018 Kidney Disease 69 0.077
77
P ATR011 Atrial Fibrillation 68 0.077
78
BRS051 Breast Disease 67 0.077
79
ISC004 Ischemia 66 0.077
80
IMM158 Immune Suppression 57 0.077
81
SYN036 Syncope 46 0.077
82
HMN016 Hemangioendothelioma 43 0.077
83
RST023 Resting Heart Rate, Variation in 42 0.077
84
GLC008 Glucose Metabolism Disease 38 0.077
85
PHC004 Phace Syndrome 36 0.077
86
ACT084 Acute Stress Disorder 35 0.077
87
P OVR042 Ovarian Cancer 82 0.070
88
P NRB001 Neuroblastoma 73 0.070
89
P PHC003 Pheochromocytoma 72 0.070
90
c ATS007 Autism Spectrum Disorder 68 0.070
91
SRC014 Sarcoma 68 0.070
92
SKN016 Skin Disease 68 0.070
93
P ART023 Arthropathy 68 0.070
94
ATM095 Autoimmune Disease 66 0.070
95
MDD011 Mood Disorder 64 0.070
96
CRD119 Cardiac Arrest 63 0.070
97
P HYP086 Hypothyroidism 62 0.070
98
HYP266 Hypoxia 61 0.070
99
P HMR003 Hemorrhagic Disease 61 0.070
100
NRM005 Neuromuscular Disease 60 0.070
101
JNT002 Joint Disorders 60 0.070
102
GT001 Gout 60 0.070
103
TRD006 Tardive Dyskinesia 59 0.070
104
SFT003 Soft Tissue Sarcoma 58 0.070
105
P OVR049 Ovarian Disease 58 0.070
106
P PNC025 Panic Disorder 57 0.070
107
IMM136 Immune System Disease 57 0.070
108
P HYP076 Hyperthyroidism 56 0.070
109
PRV006 Pervasive Developmental Disorder 56 0.070
110
P MGR003 Migraine with Aura 56 0.070
111
MGR028 Migraine with or Without Aura 1 55 0.070
112
c OVR114 Ovarian Cancer 1 54 0.070
113
SCK005 Sickle Cell Disease 54 0.070
114
P THY054 Thyrotoxic Periodic Paralysis 54 0.070
115
STM006 Stomach Disease 52 0.070
116
P CHR345 Chronic Pain 52 0.070
117
THY030 Thyroid Gland Disease 51 0.070
118
c MLG074 Malignant Mesenchymoma 51 0.070
119
ANX004 Anoxia 49 0.070
120
SKN027 Skin Conditions 48 0.070
121
KPS002 Kaposiform Hemangioendothelioma 46 0.070
122
OVR094 Ovarian Epithelial Cancer 46 0.070
123
P BLD051 Blood Coagulation Disease 38 0.070
124
FNT004 Fainting 36 0.070
125
GND003 Gonadal Disease 32 0.070
126
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.063
127
MRF001 Marfan Syndrome 75 0.063
128
SCK003 Sickle Cell Anemia 73 0.063
129
WRN001 Werner Syndrome 70 0.063
130
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.063
131
PRT036 Peritonitis 67 0.063
132
ALC007 Alcohol Dependence 65 0.063
133
P PNC044 Pancreatitis 64 0.063
134
P ART021 Arteriosclerosis 62 0.063
135
RHM027 Rheumatic Disease 62 0.063
136
P PRP029 Porphyria 62 0.063
137
THR024 Thrombosis 61 0.063
138
P DYS154 Dystonia 61 0.063
139
P DRR001 Diarrhea 60 0.063
140
HMT018 Hematopoietic Stem Cell Transplantation 58 0.063
141
URN009 Urinary System Disease 58 0.063
142
PRS042 Prostate Disease 56 0.063
143
P MSC003 Muscular Atrophy 55 0.063
144
SPS003 Spastic Diplegia 55 0.063
145
OPT003 Opiate Dependence 54 0.063
146
P CLL015 Collagen Disease 53 0.063
147
ANG054 Angina Pectoris 53 0.063
148
HMG005 Hemoglobinopathy 53 0.063
149
CRN030 Coronary Stenosis 52 0.063
150
c GRV008 Graves Disease 1 52 0.063
151
PRT018 Portal Vein Thrombosis 50 0.063
152
SCL003 Social Phobia 50 0.063
153
HPT014 Hepatorenal Syndrome 49 0.063
154
CHR008 Choroiditis 47 0.063
155
PHB001 Phobic Disorder 42 0.063
156
NRT001 Neurotic Disorder 39 0.063
157
ENT004 Enthesopathy 38 0.063
158
ADJ001 Adjustment Disorder 37 0.063
159
NNT003 Neonatal Thyrotoxicosis 28 0.063
160
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.063
161
HYP029 Hyperthyroxinemia 27 0.063
162
DFF022 Diffuse Neonatal Hemangiomatosis 26 0.063
163
P PNC035 Pancreatic Cancer 89 0.054
164
MYL069 Myeloma, Multiple 86 0.054
165
P WSK001 Wiskott-Aldrich Syndrome 76 0.054
166
P OST002 Osteoporosis 75 0.054
167
ISC006 Ischemic Heart Disease 73 0.054
168
BRN028 Brain Cancer 72 0.054
169
P MJR001 Major Depressive Disorder 70 0.054
170
P CRN018 Coronary Artery Anomaly 69 0.054
171
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.054
172
P HYD006 Hydrocephalus 68 0.054
173
APN008 Apnea, Obstructive Sleep 67 0.054
174
P KDN017 Kidney Cancer 66 0.054
175
P MCR115 Microvascular Complications of Diabetes 5 66 0.054
176
P CRN015 Cornelia De Lange Syndrome 65 0.054
177
P THL005 Thalassemia 65 0.054
178
P SLP006 Sleep Apnea 65 0.054
179
CNN005 Connective Tissue Disease 65 0.054
180
AGN016 Aging 65 0.054
181
c ACT075 Acute Myocardial Infarction 64 0.054
182
GST092 Gastroesophageal Reflux 64 0.054
183
c HPT003 Hepatitis a 63 0.054
184
P LYM025 Lymphedema 63 0.054
185
FLL027 Fallopian Tube Carcinoma 62 0.054
186
c MCR129 Microvascular Complications of Diabetes 1 62 0.054
187
c THR092 Thrombophilia Due to Thrombin Defect 61 0.054
188
P RHB003 Rhabdomyosarcoma 61 0.054
189
P GST049 Gastrointestinal System Cancer 60 0.054
190
c PRM126 Primary Peritoneal Carcinoma 59 0.054
191
P INF032 Infertility 59 0.054
192
STR039 Sturge-Weber Syndrome 59 0.054
193
ICH054 Ichthyosis, X-Linked 59 0.054
194
RSC001 Rosacea 58 0.054
195
P CRN300 Coronary Heart Disease 1 57 0.054
196
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.054
197
P SBS003 Substance Abuse 57 0.054
198
HYP060 Hyperinsulinism 56 0.054
199
P MYP006 Myopia 56 0.054
200
P THY032 Thyroiditis 56 0.054
201
c LYM130 Lymphedema, Hereditary, Ii 55 0.054
202
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.054
203
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.054
204
LYM022 Lymphangioma 53 0.054
205
NDL013 Nodular Regenerative Hyperplasia 53 0.054
206
ALC009 Alcoholic Liver Cirrhosis 53 0.054
207
CRD223 Cardiac Arrhythmia 52 0.054
208
RTN023 Retinitis 52 0.054
209
TLN003 Telangiectasis 52 0.054
210
ART140 Arteries, Anomalies of 51 0.054
211
PLS009 Plasma Cell Neoplasm 51 0.054
212
BRX001 Bruxism 51 0.054
213
DRG003 Drug Dependence 51 0.054
214
DBT008 Diabetic Angiopathy 48 0.054
215
BCK006 Back Pain 46 0.054
216
c MTR002 Mitral Valve Insufficiency 46 0.054
217
c CRN139 Cornelia De Lange Syndrome 1 46 0.054
218
LYM024 Lymphatic System Disease 45 0.054
219
VSC006 Vascular Cancer 43 0.054
220
c CHR579 Chiari Malformation Type Ii 42 0.054
221
OVR112 Ovarian Germ Cell Cancer 42 0.054
222
WBR001 Weber Syndrome 40 0.054
223
PST055 Postural Hypotension 40 0.054
224
c LYM110 Lymphedema, Hereditary, Ia 39 0.054
225
c HRD007 Hereditary Lymphedema 39 0.054
226
c CNG439 Congenital Lymphedema 37 0.054
227
c BLD140 Blood Group, I System 37 0.054
228
P GRM010 Germ Cells Tumors 37 0.054
229
ANG065 Angioma, Tufted 36 0.054
230
VSC008 Vascular Hemostatic Disease 36 0.054
231
ENG004 Engraftment Syndrome 36 0.054
232
FLL029 Fallopian Tube Disease 35 0.054
233
CNT017 Central Nervous System Origin Vertigo 30 0.054
234
DRG016 Drug Induced Dyskinesia 22 0.054
235
PNL011 Pineal Region Germinoma 20 0.054
236
P CLR023 Colorectal Cancer 98 0.044
237
STR067 Stroke, Ischemic 84 0.044
238
INS024 Insulin-Like Growth Factor I 83 0.044
239
P ART022 Arthritis 77 0.044
240
c HPT073 Hepatitis C Virus 73 0.044
241
c HPT001 Hepatitis C 73 0.044
242
P CRV035 Cervical Cancer 72 0.044
243
c CHR089 Chronic Kidney Failure 72 0.044
244
P PNM007 Pneumonia 70 0.044
245
P TBR001 Tuberous Sclerosis 69 0.044
246
CRB039 Cerebrovascular Disease 68 0.044
247
P TXP001 Toxoplasmosis 65 0.044
248
P INT068 Intestinal Disease 65 0.044
249
VRL011 Viral Infectious Disease 64 0.044
250
P SRC025 Sarcoidosis 1 63 0.044
251
P NRP001 Neuropathy 63 0.044
252
P LNG028 Long Qt Syndrome 63 0.044
253
c TBR025 Tuberous Sclerosis 1 63 0.044
254
P ALC004 Alcohol Abuse 63 0.044
255
ALC006 Alcoholic Hepatitis 62 0.044
256
P GRV001 Graves' Disease 62 0.044
257
FTT001 Fatty Liver Disease 62 0.044
258
SCH014 Schistosomiasis 62 0.044
259
VNW001 Von Willebrand's Disease 61 0.044
260
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.044
261
c LNG044 Long Qt Syndrome 1 61 0.044
262
PRP083 Porphyria, Acute Intermittent 60 0.044
263
PPL022 Papilloma 58 0.044
264
BRN038 Bronchial Disease 58 0.044
265
GLC003 Glucose Intolerance 58 0.044
266
P CRB048 Cerebral Cavernous Malformations 57 0.044
267
CNS004 Constipation 57 0.044
268
CLR003 Clear Cell Adenocarcinoma 57 0.044
269
NNL002 Nonalcoholic Steatohepatitis 56 0.044
270
HMN009 Hemangioblastoma 56 0.044
271
CLN019 Colonic Disease 55 0.044
272
P UTR058 Uterine Anomalies 55 0.044
273
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.044
274
SRS001 Serous Cystadenocarcinoma 55 0.044
275
TBC004 Tobacco Addiction 55 0.044
276
MCN001 Mucinous Adenocarcinoma 54 0.044
277
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.044
278
c ACT071 Acute Kidney Failure 54 0.044
279
GTR002 Goiter 53 0.044
280
OPT006 Optic Nerve Disease 53 0.044
281
P CRD132 Cardiac Conduction Defect 53 0.044
282
CRV040 Cervix Carcinoma 52 0.044
283
SRT004 Serotonin Syndrome 51 0.044
284
SBS004 Substance Dependence 51 0.044
285
CYS014 Cystadenocarcinoma 51 0.044
286
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.044
287
DNT012 Dental Caries 50 0.044
288
EXP004 Exophthalmos 50 0.044
289
ANG018 Angiomyolipoma 50 0.044
290
CYC008 Cyclic Vomiting Syndrome 50 0.044
291
EPT010 Epithelial-Myoepithelial Carcinoma 48 0.044
292
c ACT078 Acute Porphyria 48 0.044
293
RCR004 Recurrent Respiratory Papillomatosis 47 0.044
294
PRD004 Prediabetes Syndrome 46 0.044
295
EPD070 Epidermoid Cysts 46 0.044
296
GRD001 Giardiasis 45 0.044
297
PHC013 Phaeochromocytoma 44 0.044
298
c FML191 Familial Long Qt Syndrome 43 0.044
299
HRN003 Heroin Dependence 43 0.044
300
PRT035 Peritoneum Cancer 42 0.044
301
PRV003 Perivascular Epithelioid Cell Tumor 42 0.044
302
KDN015 Kidney Angiomyolipoma 41 0.044
303
ADR040 Adrenal Gland Pheochromocytoma 41 0.044
304
ORB013 Orbital Disease 40 0.044
305
CLR014 Clear Cell Adenoma 39 0.044
306
CRV069 Cervix Disease 39 0.044
307
DPM007 Dopamine Beta-Hydroxylase Deficiency, Congenital 38 0.044
308
P VSC018 Visceral Steatosis 38 0.044
309
RCT017 Rectal Disease 38 0.044
310
CSL001 Causalgia 38 0.044
311
ANG037 Angiomatosis 36 0.044
312
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.044
313
END034 Endocrine Exophthalmos 34 0.044
314
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.044
315
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.044
316
c CRB051 Cerebral Cavernous Malformation, Familial 20 0.044
317
AQG001 Aquagenic Pruritus 16 0.044
318
PRT124 Portal Vein, Cavernous Transformation of 12 0.044
319
P MLT020 Multiple Sclerosis 85 0.031
320
GST053 Gastric Cancer 84 0.031
321
P RTT002 Rett Syndrome 82 0.031
322
P PRK057 Parkinson Disease, Late-Onset 78 0.031
323
P INF038 Influenza 77 0.031
324
P DLT002 Dilated Cardiomyopathy 76 0.031
325
P MYS003 Myasthenia Gravis 73 0.031
326
P SCH015 Schizophrenia 71 0.031
327
P EPL164 Epilepsy 70 0.031
328
c HPT016 Hepatitis B 68 0.031
329
OBS002 Obsessive-Compulsive Disorder 68 0.031
330
DRM006 Dermatitis 67 0.031
331
P PSR002 Psoriasis 65 0.031
332
P PRS038 Personality Disorder 65 0.031
333
HYP066 Hyperglycemia 64 0.031
334
CNT047 Contact Dermatitis 64 0.031
335
P ESP024 Esophagitis 64 0.031
336
KRT001 Keratoconjunctivitis Sicca 63 0.031
337
P LPS002 Liposarcoma 61 0.031
338
P BRG001 Brugada Syndrome 61 0.031
339
P FBR017 Fibrosarcoma 61 0.031
340
ANR040 Aneurysm 61 0.031
341
ALL010 Allergic Contact Dermatitis 60 0.031
342
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.031
343
SNS001 Sensorineural Hearing Loss 59 0.031
344
P PLM034 Pulmonary Emphysema 59 0.031
345
DMY004 Demyelinating Disease 58 0.031
346
P ACT105 Acute Mountain Sickness 58 0.031
347
ZLL002 Zollinger-Ellison Syndrome 57 0.031
348
BRN004 Brain Edema 57 0.031
349
P ANG015 Angioedema 57 0.031
350
KRT006 Keratoconjunctivitis 56 0.031
351
TXC002 Toxic Encephalopathy 55 0.031
352
P SZR006 Seizure Disorder 55 0.031
353
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 54 0.031
354
RST001 Restless Legs Syndrome 54 0.031
355
P SCK002 Sick Sinus Syndrome 53 0.031
356
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.031
357
HYP005 Hypokalemia 53 0.031
358
ERY008 Erythromelalgia 53 0.031
359
INN002 Inner Ear Disease 52 0.031
360
CRN027 Corneal Neovascularization 51 0.031
361
HYP006 Hypertensive Heart Disease 51 0.031
362
KLD001 Keloids 50 0.031
363
P CRV039 Cervicitis 49 0.031
364
c MLG069 Malignant Hypertension 49 0.031
365
AST006 Astigmatism 48 0.031
366
ART004 Aortic Atherosclerosis 48 0.031
367
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 47 0.031
368
PST011 Pustulosis of Palm and Sole 47 0.031
369
CRN024 Corneal Disease 47 0.031
370
AGR002 Agoraphobia 47 0.031
371
NTR018 Neutrophilia, Hereditary 46 0.031
372
LYM127 Lymphatic Malformations 45 0.031
373
PYG006 Pyogenic Granuloma 45 0.031
374
CNT060 Central Serous Chorioretinopathy 45 0.031
375
ART008 Arteriosclerosis Obliterans 45 0.031
376
VST004 Vestibular Disease 45 0.031
377
HYP017 Hypophosphatemia 45 0.031
378
DMP001 Dumping Syndrome 45 0.031
379
PRN037 Prinzmetal's Variant Angina 44 0.031
380
MYX004 Myxedema 44 0.031
381
c PSR021 Psoriasis 14, Pustular 44 0.031
382
INT025 Intermittent Explosive Disorder 42 0.031
383
MYT011 Myotonia 41 0.031
384
P LBY004 Labyrinthitis 41 0.031
385
CRB009 Cerebritis 41 0.031
386
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.031
387
P PST059 Pustular Psoriasis 40 0.031
388
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.031
389
WTH001 Withdrawal Disorder 40 0.031
390
c SZR022 Seizures, Benign Familial Neonatal, 1 39 0.031
391
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.031
392
CNT001 Contagious Pustular Dermatitis 37 0.031
393
IRT001 Iritis 36 0.031
394
HMN035 Hemangioma-Thrombocytopenia Syndrome 36 0.031
395
CHR010 Chorioangioma 35 0.031
396
LYM095 Lymphangiomatosis 35 0.031
397
P EPL003 Epulis 34 0.031
398
NNT039 Neonatal Marfan Syndrome 33 0.031
399
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.031
400
THY001 Thyroid Crisis 30 0.031
401
c THY084 Thyrotoxic Periodic Paralysis 1 29 0.031
402
c THY083 Thyrotoxic Periodic Paralysis 2 28 0.031
403
c MYS011 Myasthenia Gravis Congenital 28 0.031
404
DRG021 Drug Metabolism, Poor, Cyp2c19-Related 28 0.031
405
DRG020 Drug Metabolism, Poor, Cyp2d6-Related 23 0.031
406
NNN007 Non-Involuting Congenital Hemangioma 20 0.031
407
MLT146 Multicore Myopathy with Mental Retardation, Short Stature, and Hypogonadotropic Hypogonadism 20 0.031
408
CRB087 Cerebral Arteriosclerosis 20 0.031
409
RPD005 Rapidly Involuting Congenital Hemangioma 18 0.031
410
INT074 Intracranial Arteriosclerosis 14 0.031
411
BRB002 Barbiturate Dependence 13 0.031
412
HMT019 Hematohidrosis 12 0.031
413
SBG002 Subglottic Angioma 8 0.031
Content
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