Search results for Halothane

683 hits were found for Halothane

# Family MCID Name MIFTS Score
1
HLT002 Halothane Hepatitis 31 39.485
2
P MLG056 Malignant Hyperthermia 66 26.054
3
PNG002 Pain Agnosia 51 8.804
4
MLG086 Malignant Hyperthermia Susceptibility 39 8.419
5
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 8.338
6
CRB004 Cerebral Artery Occlusion 45 7.836
7
c ACT134 Acute Liver Failure 59 7.578
8
MTB004 Metabolic Acidosis 48 6.738
9
P MYP004 Myopathy 67 6.596
10
ATR057 Atrioventricular Block 54 6.273
11
STT002 Status Asthmaticus 49 6.181
12
PRT037 Pertussis 65 6.078
13
c HPT003 Hepatitis a 63 5.981
14
c MLG147 Malignant Hyperthermia 1 45 5.838
15
P STR020 Strabismus 56 5.802
16
MCH006 Mechanical Strabismus 40 5.802
17
P CRD119 Cardiac Arrest 67 5.713
18
PST092 Posttransplant Acute Limbic Encephalitis 28 5.635
19
HLX001 Helix Syndrome 48 5.459
20
SBC016 Subacute Delirium 43 5.371
21
ALL029 Allergic Disease 59 5.316
22
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 5.205
23
TTN003 Tetanus 65 4.899
24
P LVR013 Liver Disease 69 4.627
25
CRT015 Carotid Artery Occlusion 45 4.619
26
HYP266 Hypoxia 57 4.486
27
ANX004 Anoxia 40 4.457
28
CRN030 Coronary Stenosis 50 4.425
29
P LNG028 Long Qt Syndrome 64 4.294
30
PLM010 Pulmonary Edema 55 4.131
31
c VRL010 Viral Hepatitis 53 4.057
32
P HPT021 Hepatitis 69 4.053
33
AMN003 Amnestic Disorder 54 3.975
34
LPP008 Lipoprotein Quantitative Trait Locus 65 3.973
35
P HYP098 Hypereosinophilic Syndrome 66 3.934
36
P MYG005 Myoglobinuria 40 3.934
37
CRD223 Cardiac Arrhythmia 63 3.914
38
P NRB001 Neuroblastoma 66 3.914
39
P ENC018 Encephalopathy 62 3.860
40
CHL068 Cholestasis 61 3.804
41
P MSC005 Muscular Dystrophy 67 3.698
42
HYP056 Hypoglycemia 65 3.634
43
SPN186 Spinal Cord Injury 61 3.524
44
ING001 Inguinal Hernia 59 3.451
45
MSL001 Measles 61 3.368
46
P PHC003 Pheochromocytoma 69 3.363
47
ADR040 Adrenal Gland Pheochromocytoma 46 3.363
48
P HYP076 Hyperthyroidism 53 3.346
49
P SZR006 Seizure Disorder 70 3.333
50
48X005 48,xyyy 39 3.299
51
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.259
52
c ACT071 Acute Kidney Failure 60 3.259
53
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.239
54
P TRM003 Tremor 48 3.235
55
CLF027 Cleft Palate, Isolated 64 3.196
56
HYP066 Hyperglycemia 61 3.188
57
c ATR087 Atrial Standstill 1 74 3.152
58
P SCL018 Scoliosis 57 3.106
59
HPT004 Hepatic Coma 43 3.092
60
HPT019 Hepatic Encephalopathy 59 3.092
61
BRN004 Brain Edema 54 3.090
62
P HYP040 Hypospadias 51 3.060
63
P SCK002 Sick Sinus Syndrome 55 3.012
64
CNT105 Central Core Disease of Muscle 59 2.964
65
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 2.960
66
CLF001 Cleft Lip 53 2.960
67
DRG002 Drug-Induced Hepatitis 42 2.934
68
INT075 Intracranial Hypertension 53 2.867
69
CRB039 Cerebrovascular Disease 66 2.853
70
CYN002 Cyanosis, Transient Neonatal 43 2.818
71
CRB090 Cerebral Hypoxia 42 2.768
72
P KDN018 Kidney Disease 72 2.719
73
HYP005 Hypokalemia 55 2.663
74
GLL048 Glial Tumor 52 2.639
75
GLM045 Glioma 63 2.639
76
P MYS005 Myositis 56 2.595
77
P ANR048 Aniridia 1 64 2.559
78
47X002 47,xyy 48 2.543
79
CYT002 Cytokine Deficiency 43 2.543
80
c PRG042 Progressive Familial Heart Block, Type Ia 66 2.515
81
MSC157 Muscular Dystrophy, Duchenne Type 79 2.491
82
LYM027 Lymphopenia 56 2.436
83
CHL014 Cholera 62 2.420
84
STT001 Status Epilepticus 59 2.420
85
TRM010 Traumatic Brain Injury 51 2.396
86
TXC005 Toxic Shock Syndrome 62 2.379
87
CRB037 Cerebral Palsy 67 2.379
88
MYT011 Myotonia 39 2.379
89
P PLM037 Pulmonary Hypertension 72 2.370
90
P EXN002 Exanthem 58 2.369
91
OCL069 Ocular Motor Apraxia 57 2.369
92
P HDC001 Headache 57 2.369
93
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.321
94
NRM005 Neuromuscular Disease 63 2.265
95
P HYP061 Hypertrophic Cardiomyopathy 69 2.265
96
NRL004 Neuroleptic Malignant Syndrome 52 2.265
97
P ADL010 Adult Respiratory Distress Syndrome 71 2.265
98
HDN002 Head Injury 44 2.265
99
BRN071 Brain Injury 50 2.265
100
P MYS003 Myasthenia Gravis 68 2.211
101
SNT005 Sinoatrial Node Disease 47 2.196
102
P PTN014 Patent Ductus Arteriosus 1 59 2.196
103
DSS009 Disseminated Intravascular Coagulation 57 2.196
104
P HRP006 Herpes Simplex 65 2.130
105
SYN036 Syncope 45 2.096
106
ART140 Arteries, Anomalies of 53 2.080
107
PYL006 Pyloric Stenosis 48 2.060
108
INT030 Intracranial Aneurysm 55 2.060
109
c ACT249 Acute Asthma 40 2.035
110
P VNT002 Ventricular Septal Defect 58 2.035
111
CRB086 Cerebral Aneurysms 40 2.035
112
c ATM011 Autoimmune Hepatitis 63 2.015
113
LPT014 Leptin Deficiency or Dysfunction 78 1.996
114
SPS057 Spasticity 42 1.986
115
RST023 Resting Heart Rate, Variation in 40 1.986
116
ANT078 Antipyrine Metabolism 23 1.986
117
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.971
118
RTN017 Retinal Detachment 60 1.908
119
GST092 Gastroesophageal Reflux 61 1.908
120
P RNV001 Renovascular Hypertension 49 1.908
121
P NRC002 Narcolepsy 56 1.905
122
P RTN016 Retinal Degeneration 52 1.905
123
ASP007 Aspiration Pneumonia 49 1.835
124
ANT019 Anterograde Amnesia 38 1.835
125
FCL014 Focal Epilepsy 53 1.823
126
QDR001 Quadriplegia 50 1.823
127
SCN049 Second-Degree Atrioventricular Block 33 1.803
128
ATM095 Autoimmune Disease 61 1.761
129
ATR089 Atrioventricular Dissociation 21 1.761
130
BCT022 Bacterial Infectious Disease 56 1.761
131
FTT001 Fatty Liver Disease 62 1.761
132
CLB002 Clubfoot 51 1.761
133
P HYP078 Hypertrophy of Breast 41 1.761
134
NWC001 Newcastle Disease 47 1.761
135
STM007 Stomatitis 54 1.761
136
ANR004 Anuria 44 1.731
137
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.682
138
c HYP595 Hypertension, Essential 85 1.682
139
P CRC039 Coarctation of Aorta 46 1.682
140
c BCT013 Bacterial Pneumonia 48 1.682
141
MNT002 Mental Depression 57 1.682
142
VRT001 Vertebral Artery Occlusion 29 1.682
143
PTH003 Pathologic Nystagmus 52 1.682
144
ISC004 Ischemia 61 1.667
145
HYP025 Hyperphosphatemia 48 1.630
146
HRT012 Heart Valve Disease 53 1.630
147
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.598
148
TRG002 Trigeminal Neuralgia 61 1.598
149
P TTR001 Tetralogy of Fallot 69 1.598
150
P INF038 Influenza 68 1.598
151
RTR001 Retrograde Amnesia 41 1.598
152
P ECL001 Eclampsia 52 1.598
153
P MYT002 Myotonic Dystrophy 51 1.598
154
MYC005 Myocardial Stunning 46 1.598
155
STR067 Stroke, Ischemic 80 1.584
156
PRP016 Paraplegia 52 1.552
157
c PRM038 Primary Agammaglobulinemia 47 1.512
158
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 1.506
159
P MJR001 Major Depressive Disorder 68 1.506
160
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.506
161
ART016 Aortic Aneurysm 68 1.506
162
BRN014 Bronchopneumonia 53 1.506
163
SPL009 Splenic Sequestration 34 1.506
164
P PNM007 Pneumonia 67 1.506
165
BRS051 Breast Disease 58 1.506
166
DPR016 Depression 65 1.506
167
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.506
168
c MGR028 Migraine with or Without Aura 1 64 1.491
169
PLY150 Polykaryocytosis Inducer 29 1.427
170
P LCT001 Lactic Acidosis 51 1.427
171
P RSP003 Respiratory Failure 74 1.427
172
PHS025 Phosphatase, Acid, of Tissues 28 1.405
173
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.405
174
P MYC007 Myocardial Infarction 70 1.405
175
P EPL164 Epilepsy 68 1.405
176
TRC022 Tricuspid Valve Insufficiency 47 1.405
177
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.405
178
c PRC016 Pre-Eclampsia 65 1.405
179
P MYT023 Myotonia Congenita 55 1.405
180
RGH001 Right Bundle Branch Block 47 1.405
181
PTT037 Pituitary Tumors 44 1.405
182
P MYC033 Myoclonus 47 1.405
183
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 1.405
184
c MJR022 Major Affective Disorder 8 38 1.378
185
c MJR024 Major Affective Disorder 9 41 1.378
186
P BPL003 Bipolar Disorder 56 1.378
187
P CTR002 Cataract 60 1.372
188
PNM008 Pneumothorax 54 1.361
189
c HPT016 Hepatitis B 62 1.332
190
CLF004 Cleft Lip/palate 57 1.291
191
EXR008 Exercise-Induced Malignant Hyperthermia 20 1.291
192
TRN015 Transient Cerebral Ischemia 63 1.291
193
CRV035 Cervical Cancer 73 1.289
194
BRK010 Burkitt Lymphoma 66 1.289
195
HRN029 Hearing Loss, Noise-Induced 37 1.289
196
c ART061 Arthrogryposis, Distal, Type 2a 58 1.289
197
ILS001 Ileus 50 1.289
198
c DLT002 Dilated Cardiomyopathy 78 1.289
199
P OTS001 Otosclerosis 49 1.289
200
GTR002 Goiter 53 1.289
201
GRN009 Granulomatous Hepatitis 34 1.289
202
VST003 Vestibular Nystagmus 25 1.289
203
CNT047 Contact Dermatitis 57 1.289
204
c SVR005 Severe Pre-Eclampsia 50 1.289
205
P MNN013 Meningitis 65 1.289
206
c JVN010 Juvenile Rheumatoid Arthritis 66 1.289
207
P SCK005 Sickle Cell Disease 56 1.289
208
MTN003 Motion Sickness 51 1.217
209
UMB002 Umbilical Hernia 47 1.217
210
WLF001 Wolff-Parkinson-White Syndrome 65 1.217
211
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.217
212
P CNT009 Central Core Myopathy 43 1.217
213
P PRP029 Porphyria 60 1.217
214
P HYP265 Hypotonia 42 1.217
215
P HML002 Hemolytic Anemia 62 1.199
216
P GLL020 Gallbladder Disease 56 1.154
217
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.152
218
HRW001 Hair Whorl 35 1.152
219
CLL010 Cellular Ependymoma 57 1.152
220
P PRD021 Periodic Paralysis 41 1.152
221
P BNG030 Benign Ependymoma 51 1.152
222
LFT001 Left Bundle Branch Hemiblock 47 1.152
223
c MLG069 Malignant Hypertension 46 1.152
224
HYP014 Hyperuricemia 51 1.152
225
HRT011 Heart Septal Defect 49 1.139
226
P MTR003 Mitral Valve Stenosis 53 1.139
227
MSC152 Muscular Dystrophy, Becker Type 69 1.054
228
SDD001 Sudden Infant Death Syndrome 60 1.054
229
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.054
230
CHP002 Chops Syndrome 47 1.054
231
P MYP006 Myopia 56 1.054
232
P BRS044 Breast Adenocarcinoma 58 1.054
233
ACT084 Acute Stress Disorder 54 1.054
234
P PRP019 Peripheral Nervous System Disease 58 1.054
235
P ART005 Arteriovenous Malformation 65 1.054
236
PST028 Post-Traumatic Stress Disorder 59 1.054
237
HYP052 Hyperkalemic Periodic Paralysis 63 0.974
238
AST054 Australia Antigen 26 0.974
239
DFC004 Deficiency Anemia 74 0.974
240
HPT046 Hepatic Veno-Occlusive Disease 62 0.974
241
INT067 Interstitial Nephritis 46 0.974
242
PRT036 Peritonitis 65 0.974
243
P DDN001 Duodenal Ulcer 53 0.974
244
DST006 Diastolic Heart Failure 45 0.974
245
OTT002 Otitis Media 71 0.962
246
P LTH003 Lethal Congenital Contracture Syndrome 41 0.962
247
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.962
248
P PRK039 Parkinsonism 55 0.962
249
STR103 Streptococcus Pneumonia 47 0.962
250
ACT078 Acute Porphyria 49 0.962
251
HMP001 Hemopericardium 47 0.962
252
P PRC012 Pericardial Effusion 50 0.962
253
LVR012 Liver Cirrhosis 63 0.962
254
c MLG150 Malignant Hyperthermia 4 19 0.871
255
c MLG151 Malignant Hyperthermia 5 27 0.871
256
c ATM111 Autoimmune Hepatitis Type 2 27 0.861
257
CNG506 Congenital Amyoplasia 27 0.861
258
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.861
259
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.861
260
P DPY001 Dupuytren Contracture 39 0.861
261
P DST002 Distal Arthrogryposis 65 0.861
262
P SLP006 Sleep Apnea 69 0.861
263
P URN019 Urinary Tract Infection 49 0.861
264
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.861
265
WST005 West Nile Virus 57 0.861
266
VRC005 Varicose Veins 60 0.861
267
P HNT016 Huntington Disease 73 0.861
268
P NRP001 Neuropathy 60 0.861
269
c FML191 Familial Long Qt Syndrome 55 0.861
270
P CYS018 Cystitis 59 0.861
271
RTN003 Retinal Ischemia 49 0.861
272
P HYD006 Hydrocephalus 61 0.861
273
PRT013 Portal Hypertension 59 0.861
274
P RTN018 Retinal Disease 53 0.861
275
MDD011 Mood Disorder 62 0.861
276
DYS073 Dysphagia 53 0.861
277
CHR284 Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids 26 0.861
278
CHD004 Chudley-Mccullough Syndrome 48 0.788
279
P HYP086 Hypothyroidism 69 0.769
280
INS024 Insulin-Like Growth Factor I 78 0.745
281
CRN234 Craniosynostosis, Adelaide Type 18 0.745
282
P AST005 Asthma 76 0.745
283
BRT054 Brittle Bone Disorder 74 0.745
284
c LKM070 Leukemia, Acute Monocytic 56 0.745
285
CRT045 Creatine Phosphokinase, Elevated Serum 39 0.745
286
ANG054 Angina Pectoris 66 0.745
287
P BRG001 Brugada Syndrome 69 0.745
288
NNL006 Non-Alcoholic Steatohepatitis 54 0.745
289
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.745
290
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.745
291
ACT088 Acute Insulin Response 39 0.745
292
ISL151 Isolated Elevated Serum Creatine Phosphokinase Levels 39 0.745
293
CRP002 Croup 42 0.745
294
EPG003 Epiglottitis 33 0.745
295
P MSC003 Muscular Atrophy 52 0.745
296
URM002 Uremia 47 0.745
297
P ART018 Aortic Valve Insufficiency 52 0.745
298
ALL006 Allergic Asthma 56 0.745
299
P THR014 Thrombocytopenia 66 0.745
300
PRC013 Pericarditis 53 0.745
301
APP008 Appendicitis 62 0.745
302
P MNC007 Monocytic Leukemia 47 0.745
303
CHL004 Cholelithiasis 49 0.745
304
ALC009 Alcoholic Liver Cirrhosis 54 0.745
305
P VSC007 Vascular Disease 63 0.745
306
ASP004 Asphyxia Neonatorum 50 0.745
307
P TMP001 Temporal Lobe Epilepsy 49 0.745
308
P GLM007 Glomerulonephritis 60 0.745
309
MNN017 Mononeuropathy 41 0.745
310
HYP026 Hypoglycemic Coma 37 0.745
311
P HYP009 Hypertrophic Pyloric Stenosis 41 0.745
312
PLM033 Pulmonary Embolism 58 0.745
313
ANS003 Anisakiasis 38 0.745
314
ACT200 Acute Monoblastic Leukemia 41 0.745
315
PRS063 Paresthesia 39 0.745
316
ANR040 Aneurysm 61 0.745
317
BDR001 Bidirectional Tachycardia 14 0.745
318
P CLS010 Cluster Headache 42 0.745
319
HNM002 Hinman Syndrome 27 0.723
320
BDD001 Budd-Chiari Syndrome 62 0.723
321
TRM026 Trimethoprim Allergy 22 0.723
322
THR024 Thrombosis 56 0.723
323
c ATM113 Autoimmune Cholangitis 30 0.723
324
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 0.723
325
CMR002 Coumarin Resistance 59 0.723
326
ACT149 Acetaminophen Metabolism 35 0.723
327
ADP007 Adie Pupil 40 0.723
328
c INF145 Infantile Liver Failure Syndrome 1 43 0.723
329
SPP004 Suppurative Cholangitis 23 0.723
330
PRT018 Portal Vein Thrombosis 50 0.723
331
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 39 0.723
332
CYT018 Cytochrome P450 2d6 Variant 26 0.723
333
ISL109 Isolated Cleft Lip 33 0.609
334
c ATM112 Autoimmune Hepatitis Type 1 32 0.609
335
LMN011 Laminopathy 34 0.609
336
TTR011 Tetraploidy 43 0.609
337
PFF001 Pfeiffer Syndrome 77 0.609
338
P ALZ034 Alzheimer Disease 87 0.609
339
P CRN300 Coronary Heart Disease 1 73 0.609
340
P FML018 Familial Mediterranean Fever 73 0.609
341
P MYM013 Moyamoya Disease 1 59 0.609
342
AGN016 Aging 54 0.609
343
MCR037 Macroglossia 44 0.609
344
P BCK002 Beckwith-Wiedemann Syndrome 62 0.609
345
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.609
346
P PRK057 Parkinson Disease, Late-Onset 80 0.609
347
PRP027 Peripheral Vascular Disease 71 0.609
349
SPS007 Spastic Cerebral Palsy 46 0.609
350
ATS010 Autosomal Recessive Disease 42 0.609
351
WTH001 Withdrawal Disorder 48 0.609
352
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.609
353
P FTL001 Fetal Alcohol Syndrome 55 0.609
354
RHM028 Rheumatic Heart Disease 56 0.609
355
P PRD006 Prader-Willi Syndrome 61 0.609
356
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.609
357
SCK003 Sickle Cell Anemia 74 0.609
359
P HLL001 Hallermann-Streiff Syndrome 49 0.609
360
HMH004 Hemihyperplasia, Isolated 41 0.609
361
HYP780 Hypoadrenocorticism, Familial 61 0.609
362
c WLM013 Wilms Tumor 1 66 0.609
363
BTT016 Batten-Turner Congenital Myopathy 53 0.609
364
P RTN024 Retinoblastoma 73 0.609
365
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.609
366
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.609
367
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.609
368
OST017 Osteomyelitis 63 0.609
369
MNC001 Monocular Esotropia 30 0.609
370
GLC003 Glucose Intolerance 54 0.609
371
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.609
372
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.609
373
c CHR684 Chronic Kidney Disease 69 0.609
374
P MTC133 Mitochondrial Myopathy 50 0.609
375
EST005 Esotropia 43 0.609
376
c PRG106 Progressive Muscular Dystrophy 32 0.609
377
P CMM008 Communicating Hydrocephalus 45 0.609
378
URT037 Urethral Stricture 42 0.609
379
CHL067 Cholecystitis 60 0.609
380
CLL003 Cellulitis 53 0.609
381
P CND004 Candidiasis 58 0.609
382
PLR007 Pleural Empyema 51 0.609
383
THR016 Thrombophlebitis 50 0.609
384
INT010 Intracranial Embolism 48 0.609
385
P INT070 Intestinal Obstruction 57 0.609
386
PLY012 Polyhydramnios 46 0.609
387
P MGR003 Migraine with Aura 52 0.609
388
GT001 Gout 64 0.609
389
PRM236 Primary Biliary Cholangitis 60 0.609
390
ALC006 Alcoholic Hepatitis 61 0.609
391
NWB001 Newborn Respiratory Distress Syndrome 56 0.609
392
THY001 Thyroid Crisis 30 0.609
393
P HMN010 Hemangioma 62 0.609
394
PPL022 Papilloma 53 0.609
395
SKN005 Skin Atrophy 41 0.609
396
P ATR010 Atrial Heart Septal Defect 58 0.609
397
c HPT015 Hepatitis D 49 0.609
398
BRC012 Brucellosis 66 0.609
399
MSC190 Muscular Disease 37 0.609
400
HMP005 Hemiplegia 54 0.609
401
MTR002 Mitral Valve Insufficiency 52 0.609
402
CHL039 Choledocholithiasis 37 0.609
403
P MTR012 Mitral Valve Disease 57 0.609
404
P CNJ013 Conjunctivitis 66 0.609
405
P SLP005 Sleep Disorder 61 0.609
406
INT066 Interstitial Lung Disease 60 0.609
407
P ART021 Arteriosclerosis 54 0.609
408
P PTS002 Ptosis 52 0.609
409
IDP070 Idiopathic Scoliosis 42 0.609
410
GST037 Gastroparesis 52 0.609
411
P URT039 Urticaria 58 0.609
412
ANK001 Ankylosis 51 0.609
413
NRM004 Neuroma 49 0.609
414
END028 Endemic Goiter 41 0.609
415
UTR020 Uterine Inversion 27 0.609
416
P CMP008 Compartment Syndrome 50 0.609
417
RFR003 Refractive Error 41 0.609
418
P ENC004 Encephalitis 61 0.609
419
P CHR345 Chronic Pain 50 0.609
420
TRP014 Triploidy 38 0.609
421
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.609
422
LRY026 Laryngeal Cleft 28 0.609
423
P PNC035 Pancreatic Cancer 86 0.544
424
OCL006 Ocular Hypertension 53 0.544
425
ACH005 Achalasia 55 0.544
426
P ACN011 Acne 57 0.544
427
BLR008 Bilirubin Metabolic Disorder 57 0.544
428
P LRY019 Laryngitis 53 0.544
429
CRC006 Carcinoid Syndrome 55 0.544
430
UNV002 Univentricular Heart 26 0.430
431
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.430
432
AML065 Amelia 29 0.430
433
c BCT007 Bacterial Meningitis 55 0.430
434
P DBT005 Diabetes Insipidus 54 0.430
435
SNG003 Single Ventricular Heart 30 0.430
436
SRT004 Serotonin Syndrome 54 0.430
437
APN006 Apnea of Prematurity 24 0.430
438
CCN009 Cocaine Intoxication 30 0.430
439
RGH006 Right Aortic Arch 29 0.430
440
P AVS003 Avascular Necrosis 41 0.430
441
STN005 St Anthony's Fire 18 0.430
442
TMP006 Temporomandibular Ankylosis 19 0.430
443
WBR001 Weber Syndrome 38 0.430
444
ATH013 Atherosclerosis Susceptibility 63 0.430
445
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.430
446
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.430
447
c SCL052 Scleroderma, Familial Progressive 61 0.430
448
SMT004 Smith-Lemli-Opitz Syndrome 70 0.430
449
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.430
450
c THY107 Thymoma, Familial 42 0.430
451
ASP026 Asplenia, Isolated Congenital 43 0.430
452
CRD132 Cardiac Conduction Defect 60 0.430
453
P LPR021 Leprosy 3 71 0.430
454
P RTN008 Retinitis Pigmentosa 80 0.430
455
ANR007 Anorexia Nervosa 60 0.430
456
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.430
457
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 0.430
458
ISP002 Isoproterenol-Mediated Vasodilatation 8 0.430
459
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.430
460
HMC014 Homocysteinemia 52 0.430
461
P KLZ004 Kala-Azar 1 41 0.430
462
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.430
463
c MYT021 Myotonic Dystrophy 1 68 0.430
464
NND010 Nondisjunction 34 0.430
465
c CRN139 Cornelia De Lange Syndrome 1 61 0.430
466
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.430
467
ALC007 Alcohol Dependence 66 0.430
468
STR039 Sturge-Weber Syndrome 61 0.430
469
c THR092 Thrombophilia Due to Thrombin Defect 74 0.430
470
WLL001 Williams-Beuren Syndrome 61 0.430
471
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 0.430
472
CYS001 Cystic Fibrosis 78 0.430
473
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.430
474
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.430
475
P APL001 Aplastic Anemia 73 0.430
476
HMN044 Human Immunodeficiency Virus Type 1 78 0.430
477
CHR100 Chronic Ulcer of Skin 57 0.430
478
FRS012 First-Degree Atrioventricular Block 39 0.430
479
THR099 Third-Degree Atrioventricular Block 42 0.430
480
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 0.430
481
GLT039 Glutathione Peroxidase Deficiency 33 0.430
482
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.430
483
PRT251 Proteinuria, Chronic Benign 57 0.430
484
ART074 Aortic Dissection 53 0.430
485
ECT026 Ectopic Pregnancy 48 0.430
486
MYL020 Myelomeningocele 51 0.430
487
P ORF002 Orofacial Cleft 43 0.430
488
INT017 Intestinal Schistosomiasis 51 0.430
489
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.430
490
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.430
491
DDN011 Duodenal Atresia 48 0.430
492
P BRN019 Bernard-Soulier Syndrome 61 0.430
493
c GRV008 Graves Disease 1 54 0.430
494
WLS001 Wilson Disease 70 0.430
495
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.430
496
P STS008 Sotos Syndrome 1 60 0.430
497
P PLV020 Pelvic Organ Prolapse 58 0.430
498
P LRY029 Laryngomalacia 48 0.430
499
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.430
500
P ORT004 Orthostatic Intolerance 63 0.430
501
c BRN108 Branchiootic Syndrome 1 62 0.430
503
c LNG048 Long Qt Syndrome 3 53 0.430
504
TRC062 Tricuspid Atresia 55 0.430
505
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.430
506
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 0.430
507
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.430
508
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.430
509
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.430
510
KWS002 Kawasaki Disease 65 0.430
511
c CHL119 Cholangitis, Primary Sclerosing 58 0.430
512
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.430
513
PRP083 Porphyria, Acute Intermittent 65 0.430
514
MGL003 Megalocornea 47 0.430
515
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.430
516
DWN001 Down Syndrome 70 0.430
517
DNY001 Denys-Drash Syndrome 57 0.430
518
c MYT029 Myotonia Congenita, Autosomal Recessive 40 0.430
519
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.430
520
P SCL057 Scoliosis, Isolated 1 40 0.430
521
OST159 Osteogenic Sarcoma 66 0.430
522
P PRR016 Pierre Robin Syndrome 50 0.430
523
GLB001 Gilbert Syndrome 53 0.430
524
HYP748 Hypertelorism 46 0.430
525
c HYP836 Hypercholesterolemia, Familial, 1 73 0.430
526
MLT157 Multiple System Atrophy 1 69 0.430
527
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 0.430
528
CLB010 Coloboma of Macula 53 0.430
529
EGS001 Egasyn 13 0.430
530
MCK029 Meckel Diverticulum 38 0.430
531
OCL052 Ocular Dominance 40 0.430
532
PCT003 Pectus Excavatum 46 0.430
533
HND015 Hand Skill, Relative 30 0.430
534
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.430
535
P HRS035 Hirschsprung Disease 1 66 0.430
536
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.430
537
GST019 Gastrointestinal Stromal Tumor 78 0.430
538
RNL077 Renal Fibrosis 46 0.430
539
NRR001 Neuroretinitis 42 0.430
540
CRR012 Cirrhotic Cardiomyopathy 22 0.430
541
RNL078 Renal Dysplasia 46 0.430
542
P VNW001 Von Willebrand's Disease 65 0.430
543
ACS001 Acoustic Neuroma 56 0.430
544
DRG024 Drug Allergy 40 0.430
545
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.430
546
ACT003 Acute Kidney Tubular Necrosis 46 0.430
547
FCL090 Facial Cleft 30 0.430
548
HPT009 Hepatopulmonary Syndrome 48 0.430
549
P BCL017 B-Cell Lymphoma 59 0.430
550
P HLP001 Holoprosencephaly 69 0.430
551
FRM001 Freemartinism 17 0.430
552
P STR001 Striatonigral Degeneration 37 0.430
553
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.430
554
ASP008 Aspiration Pneumonitis 42 0.430
555
CRC021 Carcinosarcoma 64 0.430
556
RTN023 Retinitis 46 0.430
557
INT007 Intermediate Coronary Syndrome 54 0.430
558
SKN019 Skin Melanoma 71 0.430
559
LSH001 Leishmaniasis 64 0.430
560
P CHL066 Cholangitis 52 0.430
561
P MVM001 Movement Disease 61 0.430
562
HPT022 Hepatoblastoma 54 0.430
563
SBV001 Subvalvular Aortic Stenosis 30 0.430
564
ADG002 Audiogenic Seizures 25 0.430
565
ADR057 Adrenogenital Syndrome 32 0.430
566
DBT010 Diabetic Neuropathy 54 0.430
567
P RRH023 Rare Hereditary Hemochromatosis 54 0.430
568
P ALC033 Alcohol Use Disorder 61 0.430
569
PRG001 Progressive Muscular Atrophy 41 0.430
570
c HPT001 Hepatitis C 62 0.430
571
P SKN015 Skin Carcinoma 71 0.430
572
PSD009 Pseudohermaphroditism 46 0.430
573
P SYS005 Systemic Scleroderma 74 0.430
574
MTS001 Mutism 44 0.430
575
ACQ007 Acquired Immunodeficiency Syndrome 59 0.430
576
PLM041 Pulmonary Valve Stenosis 50 0.430
577
SMN007 Seminoma 42 0.430
578
P PLY018 Polycythemia 56 0.430
579
OST012 Osteoarthritis 77 0.430
581
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.430
582
SLC006 Silicosis 56 0.430
583
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.430
584
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.430
585
HMS001 Hemosiderosis 48 0.430
586
PLC002 Plica Syndrome 35 0.430
587
P NTR004 Neutropenia 63 0.430
588
VRC001 Varicocele 48 0.430
589
CNN003 Conn's Syndrome 79 0.430
590
NRG002 Neurogenic Bladder 55 0.430
591
LWC001 Low Compliance Bladder 45 0.430
592
P SPN046 Spinal Muscular Atrophy 63 0.430
593
P GLL022 Guillain-Barre Syndrome 60 0.430
594
SCK001 Sick Building Syndrome 33 0.430
595
c ACT027 Acute Pancreatitis 60 0.430
596
P HYP069 Hyperparathyroidism 62 0.430
597
SQM002 Squamous Cell Papilloma 46 0.430
598
P MLN008 Melanoma 76 0.430
599
P SCL009 Sclerosing Cholangitis 48 0.430
600
RTN020 Retinal Vascular Disease 46 0.430
601
RYS001 Reye Syndrome 49 0.430
602
TST015 Testicular Disease 42 0.430
603
P HMR003 Hemorrhagic Disease 59 0.430
604
P CRN037 Craniosynostosis 68 0.430
605
NNT012 Neonatal Jaundice 53 0.430
606
FCL012 Facial Paralysis 49 0.430
607
SCH014 Schistosomiasis 56 0.430
608
OPT003 Opiate Dependence 49 0.430
609
BRB002 Barbiturate Dependence 28 0.430
610
P GLY013 Glycogen Storage Disease 60 0.430
611
P END044 Endometriosis 62 0.430
612
ATN004 Autonomic Neuropathy 42 0.430
613
IRN001 Iron Deficiency Anemia 58 0.430
614
HPT014 Hepatorenal Syndrome 49 0.430
615
P RNL015 Renal Hypertension 45 0.430
616
HYD002 Hydronephrosis 58 0.430
617
SPN369 Spinal Disease 44 0.430
618
MCS002 Mucositis 56 0.430
619
LPR001 Lepromatous Leprosy 49 0.430
620
RBS001 Rabies 58 0.430
621
CRD001 Cardiac Tamponade 43 0.430
622
P CRN015 Cornelia De Lange Syndrome 67 0.430
623
P EMR001 Emery-Dreifuss Muscular Dystrophy 62 0.430
624
P HYP024 Hypoparathyroidism 55 0.430
625
CNS002 Constrictive Pericarditis 40 0.430
626
ESP020 Esophageal Atresia 60 0.430
627
CNG034 Congestive Heart Failure 69 0.430
628
BRN024 Bronchitis 67 0.430
629
AMP007 Amphetamine Abuse 36 0.430
630
ADJ001 Adjustment Disorder 47 0.430
631
P PNC044 Pancreatitis 61 0.430
632
c ESS001 Essential Tremor 57 0.430
633
P INF032 Infertility 57 0.430
634
P TRT010 Teratoma 51 0.430
635
CRB025 Carbohydrate Metabolic Disorder 40 0.430
636
P SBS003 Substance Abuse 54 0.430
637
LPD008 Lipid Metabolism Disorder 62 0.430
638
MRP001 Morphine Dependence 42 0.430
639
SYN007 Synovitis 55 0.430
640
P EPD016 Epidermolysis Bullosa 53 0.430
641
P THY023 Thymoma 64 0.430
642
P MTR014 Motor Neuron Disease 65 0.430
643
CRT016 Carotid Artery Disease 52 0.430
644
CRT004 Carotid Artery Thrombosis 39 0.430
645
BRN002 Bronchiolitis 57 0.430
646
OBS004 Obstructive Hydrocephalus 45 0.430
647
P GND004 Gonadal Dysgenesis 47 0.430
648
P EHL001 Ehlers-Danlos Syndrome 58 0.430
649
DBT002 Diabetic Autonomic Neuropathy 41 0.430
650
SPN033 Spontaneous Ocular Nystagmus 25 0.430
651
P NRM002 Normal Pressure Hydrocephalus 49 0.430
652
CHR073 Choreatic Disease 54 0.430
653
IRN002 Iron Metabolism Disease 57 0.430
654
HYP080 Hypogonadism 50 0.430
655
HLL004 Hellp Syndrome 53 0.430
656
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.430
657
KCN019 Kcnk9 Imprinting Syndrome 22 0.430
658
P NRF002 Neurofibromatosis 57 0.430
659
P MYC008 Myocarditis 59 0.430
660
GRN017 Granulocytopenia 42 0.430
661
MBM001 Meibomian Cyst 36 0.430
662
P HYP055 Hypoplastic Left Heart Syndrome 65 0.430
663
IRR002 Irritable Bowel Syndrome 65 0.430
664
HNS001 Hansen's Disease 32 0.430
665
HPR003 Heparin-Induced Thrombocytopenia 47 0.430
666
MST020 Mast Cell Activation Syndrome 28 0.430
667
P CRB088 Cerebral Atrophy 33 0.430
668
ATN005 Autonomic Dysfunction 46 0.430
669
FNT004 Fainting 29 0.430
670
P PRD017 Periodic Paralyses 24 0.430
671
MLT028 Multiminicore Disease 43 0.430
672
OPD006 Opioid Addiction 48 0.430
673
RYN005 Raynaud Phenomenon 45 0.430
674
P DYS021 Dysautonomia 38 0.430
675
P HYP263 Hypersomnia 41 0.430
676
HYP264 Hypertonia 36 0.430
677
P MRC003 Mercury Poisoning 49 0.430
678
BRN056 Bronchopulmonary Dysplasia 56 0.430
679
DWR001 Dwarfism 44 0.430
680
LRY027 Laryngeal Papillomatosis 21 0.430
681
PNF002 Painful Legs and Moving Toes Syndrome 14 0.430
682
PRT058 Pure Autonomic Failure 58 0.430
683
GGN002 Gigantism 33 0.430
Content
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