Search results for Propofol

962 hits were found for Propofol

# Family MCID Name MIFTS Score
1
PNG002 Pain Agnosia 51 0.439
2
SBC016 Subacute Delirium 44 0.322
3
AMN003 Amnestic Disorder 54 0.310
4
ISC004 Ischemia 58 0.272
5
DPR016 Depression 63 0.237
6
MNT002 Mental Depression 58 0.227
7
MTB004 Metabolic Acidosis 50 0.217
8
P SZR006 Seizure Disorder 56 0.215
9
STT001 Status Epilepticus 60 0.214
10
ANX010 Anxiety 73 0.213
11
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.200
12
c PNS012 Paine Syndrome 61 0.199
13
P SLP006 Sleep Apnea 69 0.188
14
HYP266 Hypoxia 57 0.188
15
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.181
16
48X005 48,xyyy 39 0.181
17
VSL002 Visual Epilepsy 59 0.175
18
c HYP595 Hypertension, Essential 84 0.164
19
P CRD119 Cardiac Arrest 67 0.161
20
P STR020 Strabismus 55 0.159
21
MCH006 Mechanical Strabismus 42 0.159
22
BRN071 Brain Injury 49 0.156
23
P MYC033 Myoclonus 46 0.156
24
CHL079 Children's Interstitial Lung Disease 26 0.155
25
TRM010 Traumatic Brain Injury 51 0.150
26
c FNC043 Fanconi Anemia, Complementation Group E 62 0.148
27
OCL069 Ocular Motor Apraxia 51 0.148
28
ATX019 Ataxia with Vitamin E Deficiency 42 0.147
29
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.142
30
ADL002 Adult Syndrome 70 0.142
31
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.142
32
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.142
33
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.142
34
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.142
35
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.142
36
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.142
37
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.142
38
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.142
39
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.142
40
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.142
41
P RSP003 Respiratory Failure 74 0.140
42
P KDN018 Kidney Disease 72 0.140
43
LPP008 Lipoprotein Quantitative Trait Locus 62 0.140
44
P MLG056 Malignant Hyperthermia 67 0.138
45
LVR012 Liver Cirrhosis 62 0.138
46
P HYP750 Hypertriglyceridemia, Familial 62 0.136
47
P HRT032 Heart Disease 75 0.134
48
P LVR013 Liver Disease 68 0.134
49
P TRN020 Turner Syndrome 67 0.134
50
P LCT001 Lactic Acidosis 51 0.134
51
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.134
52
HDN002 Head Injury 46 0.133
53
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.131
54
APN008 Apnea, Obstructive Sleep 64 0.129
55
P CLR023 Colorectal Cancer 99 0.127
56
P PRP029 Porphyria 62 0.127
57
P HDC001 Headache 57 0.127
58
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.125
59
CRB039 Cerebrovascular Disease 67 0.125
60
P PNC044 Pancreatitis 61 0.125
61
c RHB024 Rhabdomyosarcoma 2 67 0.123
62
TXC005 Toxic Shock Syndrome 62 0.123
63
P ENC018 Encephalopathy 61 0.123
64
P CTR002 Cataract 60 0.123
65
ART140 Arteries, Anomalies of 52 0.121
66
c MGR028 Migraine with or Without Aura 1 67 0.119
67
P CRN300 Coronary Heart Disease 1 63 0.119
68
P SCL018 Scoliosis 60 0.119
69
STR067 Stroke, Ischemic 81 0.117
70
c ACT027 Acute Pancreatitis 60 0.117
71
CRB004 Cerebral Artery Occlusion 45 0.117
72
CYT002 Cytokine Deficiency 42 0.115
73
P EPL164 Epilepsy 71 0.113
74
c ACT071 Acute Kidney Failure 60 0.111
75
P OPT006 Optic Nerve Disease 60 0.111
76
P VSC007 Vascular Disease 63 0.108
77
HYP066 Hyperglycemia 61 0.108
78
ANR040 Aneurysm 59 0.108
79
P TRM003 Tremor 54 0.108
80
P ATR011 Atrial Fibrillation 66 0.106
81
INT075 Intracranial Hypertension 53 0.106
82
LPT014 Leptin Deficiency or Dysfunction 74 0.104
83
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.104
84
47X002 47,xyy 49 0.104
85
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.101
86
END086 End Stage Renal Disease 51 0.101
87
P CHR345 Chronic Pain 44 0.101
88
HPT019 Hepatic Encephalopathy 60 0.099
89
P ALC033 Alcohol Use Disorder 58 0.099
90
HPT004 Hepatic Coma 45 0.099
91
ANT019 Anterograde Amnesia 38 0.099
92
P GST053 Gastric Cancer 83 0.096
93
P PHC003 Pheochromocytoma 71 0.096
94
P PNM007 Pneumonia 68 0.096
95
P ADL010 Adult Respiratory Distress Syndrome 65 0.096
96
ADR040 Adrenal Gland Pheochromocytoma 46 0.096
97
P LNG032 Lung Cancer 98 0.094
98
P BRS047 Breast Cancer 97 0.094
99
P CNR004 Cone-Rod Dystrophy 2 73 0.094
100
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.094
101
P MJR001 Major Depressive Disorder 68 0.091
102
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.091
103
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.091
104
VRC005 Varicose Veins 60 0.091
105
P BCL017 B-Cell Lymphoma 58 0.091
106
HRT012 Heart Valve Disease 53 0.091
107
NRT001 Neurotic Disorder 53 0.091
108
LNG099 Lung Disease 60 0.088
109
INT030 Intracranial Aneurysm 56 0.088
110
END040 Endogenous Depression 55 0.088
111
P PRK057 Parkinson Disease, Late-Onset 78 0.086
112
BRN028 Brain Cancer 74 0.086
113
CNG034 Congestive Heart Failure 69 0.086
114
TTN003 Tetanus 65 0.086
115
P DYS154 Dystonia 65 0.086
116
P MVM001 Movement Disease 63 0.086
117
ING001 Inguinal Hernia 60 0.086
118
ADN018 Adenoma 59 0.086
119
ENT001 Enterocele 39 0.086
120
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.086
121
P PRS040 Prostate Cancer 97 0.083
122
P PNC035 Pancreatic Cancer 84 0.083
123
P MYC007 Myocardial Infarction 70 0.083
124
CRB037 Cerebral Palsy 69 0.083
125
P CRD246 Cardiovascular System Disease 57 0.083
126
CRB086 Cerebral Aneurysms 40 0.083
127
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.080
128
P MYS003 Myasthenia Gravis 68 0.080
129
ALC007 Alcohol Dependence 66 0.080
130
PRP083 Porphyria, Acute Intermittent 64 0.080
131
NWB001 Newborn Respiratory Distress Syndrome 58 0.080
132
PLM010 Pulmonary Edema 54 0.080
133
P MYT002 Myotonic Dystrophy 49 0.080
134
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.080
135
MCR011 Microinvasive Gastric Cancer 43 0.080
136
c PRS136 Prostate Cancer, Hereditary, 6 33 0.080
137
c PRS130 Prostate Cancer, Hereditary, 8 32 0.080
138
P SLP005 Sleep Disorder 59 0.077
139
c ACT073 Acute Leukemia 58 0.077
140
PTH003 Pathologic Nystagmus 52 0.077
141
THR016 Thrombophlebitis 51 0.077
142
ASP007 Aspiration Pneumonia 48 0.077
143
RDN001 Reading Disorder 40 0.077
144
P NRB001 Neuroblastoma 72 0.073
145
c CHR684 Chronic Kidney Disease 70 0.073
146
ART016 Aortic Aneurysm 69 0.073
147
P HYD006 Hydrocephalus 66 0.073
148
P EXN002 Exanthem 57 0.073
149
HYP005 Hypokalemia 55 0.073
150
P HYP076 Hyperthyroidism 55 0.073
151
FDL002 Food Allergy 51 0.073
152
WTH001 Withdrawal Disorder 48 0.073
153
LPT006 Leptin Receptor Deficiency 48 0.073
154
P HPT023 Hepatocellular Carcinoma 100 0.070
155
ANG054 Angina Pectoris 66 0.070
156
c FML001 Familial Atrial Fibrillation 65 0.070
157
P LRS001 Larsen Syndrome 62 0.070
158
ALL026 Allergic Hypersensitivity Disease 62 0.070
159
SPN186 Spinal Cord Injury 60 0.070
160
CRD223 Cardiac Arrhythmia 60 0.070
161
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.070
162
PNM008 Pneumothorax 56 0.070
163
GST050 Gastrointestinal System Disease 56 0.070
164
BRN004 Brain Edema 56 0.070
165
AGN016 Aging 56 0.070
166
CLF001 Cleft Lip 53 0.070
167
c GLL024 Gallbladder Disease 1 53 0.070
168
CYN002 Cyanosis, Transient Neonatal 45 0.070
169
49X006 49, Xxxxy Syndrome 41 0.070
170
ANX004 Anoxia 40 0.070
171
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.070
172
RSP007 Respiratory Distress Syndrome, Infant 30 0.070
173
P SCH015 Schizophrenia 74 0.066
174
P BRG001 Brugada Syndrome 71 0.066
175
P MYP004 Myopathy 70 0.066
176
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.066
177
P MSC005 Muscular Dystrophy 66 0.066
178
c MCL013 Mucolipidosis Iv 66 0.066
179
PLM033 Pulmonary Embolism 59 0.066
180
P INF032 Infertility 57 0.066
181
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.066
182
AYM001 Ayme-Gripp Syndrome 57 0.066
183
P NRP001 Neuropathy 56 0.066
184
ATR057 Atrioventricular Block 55 0.066
185
CLF004 Cleft Lip/palate 54 0.066
186
ILS001 Ileus 51 0.066
187
BHR001 Behr Syndrome 51 0.066
188
DYS073 Dysphagia 50 0.066
189
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.066
190
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.066
191
CLN045 Colonic Benign Neoplasm 46 0.066
192
RTR001 Retrograde Amnesia 44 0.066
193
OST012 Osteoarthritis 78 0.063
194
P ATS364 Autism 70 0.063
195
GST092 Gastroesophageal Reflux 67 0.063
196
P PLM037 Pulmonary Hypertension 67 0.063
197
P DMN002 Dementia 66 0.063
198
KHL003 Kohlschutter-Tonz Syndrome 65 0.063
199
P ART005 Arteriovenous Malformation 65 0.063
200
PPL049 Papillon-Lefevre Syndrome 65 0.063
201
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.063
202
P GLM045 Glioma 63 0.063
203
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.063
204
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.063
205
P GLL020 Gallbladder Disease 57 0.063
206
CHL067 Cholecystitis 57 0.063
207
P BPL003 Bipolar Disorder 56 0.063
208
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.063
209
CRT013 Carotid Stenosis 50 0.063
210
CHL004 Cholelithiasis 49 0.063
211
GLL048 Glial Tumor 45 0.063
212
PTT037 Pituitary Tumors 44 0.063
213
GST020 Gastric Antral Vascular Ectasia 41 0.063
214
c MJR024 Major Affective Disorder 9 41 0.063
215
c MJR022 Major Affective Disorder 8 38 0.063
216
ESP021 Esophageal Cancer 90 0.058
217
c ATR087 Atrial Standstill 1 75 0.058
218
c THR092 Thrombophilia Due to Thrombin Defect 73 0.058
219
P LKM002 Leukemia 68 0.058
220
P LNG028 Long Qt Syndrome 66 0.058
221
P MNN013 Meningitis 66 0.058
222
c SML038 Small Cell Cancer of the Lung 65 0.058
223
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.058
224
RTN017 Retinal Detachment 61 0.058
225
THY029 Thyroid Carcinoma 59 0.058
226
IGR001 Ige Responsiveness, Atopic 59 0.058
227
CNS004 Constipation 58 0.058
228
P MYM013 Moyamoya Disease 1 57 0.058
229
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.058
230
P SBS003 Substance Abuse 55 0.058
231
INT007 Intermediate Coronary Syndrome 55 0.058
232
BLR001 Biliary Atresia 50 0.058
233
c CNG216 Congenital Hydrocephalus 47 0.058
234
SYN036 Syncope 45 0.058
235
CRT015 Carotid Artery Occlusion 45 0.058
236
PLY068 Polysubstance Abuse 43 0.058
237
P HYP265 Hypotonia 43 0.058
238
P MJR007 Major Affective Disorder 1 43 0.058
239
IDP070 Idiopathic Scoliosis 42 0.058
240
P OVR042 Ovarian Cancer 88 0.054
241
P ALZ034 Alzheimer Disease 88 0.054
242
P BLD134 Bladder Cancer 79 0.054
243
P ART022 Arthritis 69 0.054
244
PSY004 Psychotic Disorder 67 0.054
245
WLF001 Wolff-Parkinson-White Syndrome 66 0.054
246
HYP056 Hypoglycemia 66 0.054
247
KRT019 Keratitis, Hereditary 65 0.054
248
c ART101 Aortic Valve Disease 2 65 0.054
249
P ESP024 Esophagitis 62 0.054
250
NTR005 Nutritional Deficiency Disease 62 0.054
251
PRT013 Portal Hypertension 59 0.054
252
EYD002 Eye Disease 58 0.054
253
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.054
254
c ACT075 Acute Myocardial Infarction 57 0.054
255
P AGN002 Agnosia 55 0.054
256
P PTT006 Pituitary Adenoma 55 0.054
257
SPS003 Spastic Diplegia 51 0.054
258
P HYP040 Hypospadias 51 0.054
259
P CHL066 Cholangitis 51 0.054
260
P TMP001 Temporal Lobe Epilepsy 50 0.054
261
P OBS001 Obstructive Jaundice 50 0.054
262
PRP007 Priapism 47 0.054
263
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.054
264
CRD137 Cardiogenic Shock 47 0.054
265
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.054
266
c PRM038 Primary Agammaglobulinemia 44 0.054
267
CRB090 Cerebral Hypoxia 44 0.054
268
DRG024 Drug Allergy 42 0.054
269
c MJR008 Major Affective Disorder 2 35 0.054
270
c MJR023 Major Affective Disorder 7 33 0.054
271
c MJR003 Major Affective Disorder 6 33 0.054
272
c MJR006 Major Affective Disorder 5 33 0.054
273
c MJR004 Major Affective Disorder 4 28 0.054
274
CRV035 Cervical Cancer 76 0.049
275
GLB015 Glioblastoma Multiforme 75 0.049
276
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.049
277
P LYM118 Lymphoma 68 0.049
278
CHL065 Cholangiocarcinoma 68 0.049
279
c ATS007 Autism Spectrum Disorder 67 0.049
280
OST159 Osteogenic Sarcoma 66 0.049
281
P PRS038 Personality Disorder 65 0.049
282
P DBT009 Diabetes Mellitus 64 0.049
283
P HYP069 Hyperparathyroidism 63 0.049
284
CHN016 Cohen Syndrome 63 0.049
285
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.049
286
CHL068 Cholestasis 61 0.049
287
P ENC004 Encephalitis 61 0.049
288
PNM010 Pneumothorax, Primary Spontaneous 60 0.049
289
P ATR010 Atrial Heart Septal Defect 60 0.049
290
P SNS001 Sensorineural Hearing Loss 60 0.049
291
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.049
292
PST028 Post-Traumatic Stress Disorder 58 0.049
293
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.049
294
P ESP035 Esophagitis, Eosinophilic, 1 57 0.049
295
P URF003 Urofacial Syndrome 1 57 0.049
296
P MTC069 Mitochondrial Disorders 56 0.049
297
P DYS193 Dystonia 11, Myoclonic 55 0.049
298
URN010 Urinary Tract Obstruction 55 0.049
299
BRN038 Bronchial Disease 53 0.049
300
MTN003 Motion Sickness 53 0.049
301
P INT068 Intestinal Disease 53 0.049
302
MCN017 Meconium Ileus 52 0.049
303
P RCT021 Rectum Cancer 52 0.049
304
INT079 Intrahepatic Cholangiocarcinoma 51 0.049
305
LNG031 Lung Benign Neoplasm 51 0.049
306
STT002 Status Asthmaticus 50 0.049
307
HRT011 Heart Septal Defect 50 0.049
308
ART017 Aortic Disease 49 0.049
309
URN009 Urinary System Disease 48 0.049
310
ACT084 Acute Stress Disorder 47 0.049
311
TST044 Testicular Torsion 47 0.049
312
LYM019 Lymphosarcoma 46 0.049
313
EGG001 Egg Allergy 44 0.049
314
P MYG005 Myoglobinuria 44 0.049
315
TRP009 Triple X Syndrome 42 0.049
316
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.049
317
ANG049 Angioedema Induced by Ace Inhibitors 40 0.049
318
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.044
319
P LNG064 Lung Cancer Susceptibility 3 78 0.044
320
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.044
321
MSC157 Muscular Dystrophy, Duchenne Type 72 0.044
322
DFC004 Deficiency Anemia 70 0.044
323
DWN001 Down Syndrome 70 0.044
324
P TTR001 Tetralogy of Fallot 70 0.044
325
P OCL013 Oculodentodigital Dysplasia 69 0.044
326
P HYP086 Hypothyroidism 69 0.044
327
P LKM062 Leukemia, Acute Lymphoblastic 69 0.044
328
BRN024 Bronchitis 68 0.044
329
P THR014 Thrombocytopenia 67 0.044
330
P HPT021 Hepatitis 67 0.044
331
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.044
332
PRP001 Propionic Acidemia 65 0.044
333
NRF007 Neurofibroma 64 0.044
334
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.044
335
P ADN016 Adenocarcinoma 64 0.044
336
TRN015 Transient Cerebral Ischemia 63 0.044
337
SQM006 Squamous Cell Carcinoma 60 0.044
338
c HPT016 Hepatitis B 59 0.044
339
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.044
340
P INT070 Intestinal Obstruction 58 0.044
341
DSS008 Disease of Mental Health 58 0.044
342
LYM027 Lymphopenia 58 0.044
343
GLS018 Glass Syndrome 57 0.044
344
APH002 Aphasia 57 0.044
345
CMM005 Common Cold 57 0.044
346
CMR002 Coumarin Resistance 56 0.044
347
c ACT134 Acute Liver Failure 56 0.044
348
SPN041 Spinal Cord Disease 56 0.044
349
P NRF002 Neurofibromatosis 56 0.044
350
P GST044 Gastritis 56 0.044
351
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.044
352
FCL014 Focal Epilepsy 54 0.044
353
P INF037 Inflammatory Bowel Disease 54 0.044
354
P LTR001 Lateral Sclerosis 54 0.044
355
MYM001 Myoma 54 0.044
356
PTT009 Pituitary Gland Disease 54 0.044
357
P PTS002 Ptosis 53 0.044
358
TXC002 Toxic Encephalopathy 53 0.044
359
ART074 Aortic Dissection 52 0.044
360
P CMP008 Compartment Syndrome 49 0.044
361
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
362
OPD006 Opioid Addiction 48 0.044
363
CLN019 Colonic Disease 47 0.044
364
MYC005 Myocardial Stunning 46 0.044
365
P MTH007 Methemoglobinemia 46 0.044
366
ASP008 Aspiration Pneumonitis 45 0.044
367
PNT038 Peanut Allergy 45 0.044
368
BCK006 Back Pain 42 0.044
369
P INT260 Intracranial Berry Aneurysm 39 0.044
370
c PLM022 Pulmonary Valve Insufficiency 39 0.044
371
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.044
372
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.044
373
CHL013 Cholecystolithiasis 37 0.044
374
CRD220 Cardiac Valvular Defect, Developmental 29 0.044
375
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.044
376
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.044
377
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.038
378
c DLT002 Dilated Cardiomyopathy 79 0.038
379
AST005 Asthma 76 0.038
380
P OST002 Osteoporosis 74 0.038
381
c EXD008 Exudative Vitreoretinopathy 1 71 0.038
382
P SRC025 Sarcoidosis 1 70 0.038
383
P BLD062 Bile Duct Cancer 67 0.038
385
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.038
386
NRM005 Neuromuscular Disease 64 0.038
387
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.038
388
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.038
389
c HPT003 Hepatitis a 62 0.038
390
P ART023 Arthropathy 62 0.038
391
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.038
392
P HYP097 Hyperekplexia 61 0.038
393
FTT001 Fatty Liver Disease 61 0.038
394
DRM006 Dermatitis 61 0.038
395
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.038
396
P KDN017 Kidney Cancer 60 0.038
397
ORL011 Oral Cancer 60 0.038
398
P MYC008 Myocarditis 59 0.038
399
CRD132 Cardiac Conduction Defect 58 0.038
400
P BNC003 Bone Cancer 58 0.038
401
CPR004 Coproporphyria, Hereditary 57 0.038
402
THR024 Thrombosis 57 0.038
403
INT303 Intracranial Hypertension, Idiopathic 57 0.038
404
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.038
405
ALL006 Allergic Asthma 56 0.038
406
HMT008 Hematuria, Benign Familial 56 0.038
407
c ESS001 Essential Tremor 56 0.038
408
VRG001 Variegate Porphyria 56 0.038
409
NRL004 Neuroleptic Malignant Syndrome 56 0.038
410
P PLY019 Polyneuropathy 56 0.038
411
LMB062 Limb Ischemia 55 0.038
412
P DRR001 Diarrhea 55 0.038
413
ESN005 Eosinophilic Gastroenteritis 55 0.038
414
CHR101 Char Syndrome 55 0.038
415
HMP005 Hemiplegia 55 0.038
416
CRT017 Cartilage Disease 54 0.038
417
P ART021 Arteriosclerosis 54 0.038
418
CLL003 Cellulitis 54 0.038
419
NNL006 Non-Alcoholic Steatohepatitis 54 0.038
420
PNC001 Pancytopenia 54 0.038
421
P TCD001 Tic Disorder 53 0.038
422
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.038
423
DNT012 Dental Caries 53 0.038
424
PRP016 Paraplegia 52 0.038
425
P MSC003 Muscular Atrophy 52 0.038
426
FML037 Female Breast Cancer 52 0.038
427
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.038
428
LMY002 Leiomyoma 52 0.038
429
c PNC106 Pancreatic Agenesis 1 51 0.038
430
ESP002 Esophageal Varix 51 0.038
431
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.038
432
TNG007 Tongue Carcinoma 51 0.038
433
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.038
434
RTN003 Retinal Ischemia 50 0.038
435
RSP006 Respiratory System Disease 50 0.038
436
c INF145 Infantile Liver Failure Syndrome 1 50 0.038
437
P MTC133 Mitochondrial Myopathy 49 0.038
438
LFT001 Left Bundle Branch Hemiblock 49 0.038
439
GST049 Gastrointestinal System Cancer 49 0.038
440
MTC005 Mitochondrial Metabolism Disease 49 0.038
441
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.038
442
PNC034 Pancreas Disease 48 0.038
443
P TRT019 Torticollis 48 0.038
444
HRN026 Hernia, Hiatus 47 0.038
445
P BLR006 Biliary Tract Disease 47 0.038
446
STM006 Stomach Disease 47 0.038
447
GST071 Gastrointestinal Carcinoma 47 0.038
448
UMB002 Umbilical Hernia 46 0.038
449
OPD001 Opioid Abuse 46 0.038
450
P HRN001 Horner's Syndrome 45 0.038
451
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.038
452
P PRD021 Periodic Paralysis 45 0.038
453
SPS057 Spasticity 45 0.038
454
DWR001 Dwarfism 44 0.038
455
PPL001 Papillary Adenoma 44 0.038
456
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.038
457
IDP033 Idiopathic Edema 44 0.038
458
MRG013 Mirage Syndrome 43 0.038
459
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.038
460
P CRN035 Cranial Nerve Palsy 42 0.038
461
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.038
462
c CHR091 Chronic Meningitis 41 0.038
463
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.038
464
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.038
465
HYP344 Hyperthyroidism, Familial Gestational 39 0.038
466
SPR024 Supratentorial Cancer 39 0.038
467
FML039 Female Reproductive System Disease 39 0.038
468
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.038
469
TRC005 Tracheal Stenosis 38 0.038
470
BLR028 Biliary Atresia, Extrahepatic 37 0.038
471
ORB006 Orbital Cellulitis 37 0.038
472
DDN027 Duodenum Disease 37 0.038
473
MYT011 Myotonia 34 0.038
474
DDN009 Duodenal Obstruction 34 0.038
475
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.038
477
CRT009 Critical Illness Polyneuropathy 32 0.038
478
PLY150 Polykaryocytosis Inducer 31 0.038
479
HMC012 Hemicrania Continua 28 0.038
480
PRK076 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 28 0.038
481
VLK001 Volkmann Contracture 25 0.038
482
NWD001 New Daily-Persistent Headache 21 0.038
483
P GLM040 Glioma Susceptibility 1 81 0.031
484
P RTT002 Rett Syndrome 80 0.031
485
PFF001 Pfeiffer Syndrome 79 0.031
486
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.031
487
CRH001 Crohn's Disease 74 0.031
488
P HNT016 Huntington Disease 72 0.031
489
OTT002 Otitis Media 72 0.031
490
PRP027 Peripheral Vascular Disease 71 0.031
491
P HYP061 Hypertrophic Cardiomyopathy 70 0.031
492
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.031
493
P CRN037 Craniosynostosis 68 0.031
494
P MYC084 Mycobacterium Tuberculosis 1 68 0.031
495
OBS002 Obsessive-Compulsive Disorder 68 0.031
496
P PRP003 Porphyria Cutanea Tarda 67 0.031
497
GLL008 Gilles De La Tourette Syndrome 66 0.031
498
P NRV007 Nervous System Disease 66 0.031
499
P MTR014 Motor Neuron Disease 65 0.031
500
BRR014 Barrett Esophagus 65 0.031
501
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.031
502
ATH013 Atherosclerosis Susceptibility 65 0.031
503
CRB011 Cerebrotendinous Xanthomatosis 65 0.031
504
PRT036 Peritonitis 64 0.031
505
ART002 Arts Syndrome 64 0.031
506
MSC007 Muscle Hypertrophy 64 0.031
507
KRN002 Kearns-Sayre Syndrome 63 0.031
508
c PRC016 Pre-Eclampsia 63 0.031
509
P THR117 Three M Syndrome 1 63 0.031
510
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.031
511
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.031
512
P VSC011 Vasculitis 62 0.031
513
P ORT004 Orthostatic Intolerance 62 0.031
514
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.031
515
APP008 Appendicitis 61 0.031
516
P MYL006 Myeloid Leukemia 60 0.031
517
TRG002 Trigeminal Neuralgia 60 0.031
518
INT066 Interstitial Lung Disease 60 0.031
519
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.031
520
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.031
521
INS001 Insulinoma 60 0.031
522
HYD002 Hydronephrosis 60 0.031
523
STF001 Stiff-Person Syndrome 60 0.031
524
P GLY013 Glycogen Storage Disease 60 0.031
525
P BRS044 Breast Adenocarcinoma 59 0.031
526
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.031
527
CMP010 Complex Regional Pain Syndrome 58 0.031
528
P URT039 Urticaria 58 0.031
529
P PRP019 Peripheral Nervous System Disease 58 0.031
530
BRN056 Bronchopulmonary Dysplasia 57 0.031
531
TNS005 Tonsillitis 57 0.031
532
STR081 Stormorken Syndrome 57 0.031
533
HMR039 Hemorrhage, Intracerebral 57 0.031
534
P PLY011 Polycystic Ovary Syndrome 56 0.031
535
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.031
536
c GRV008 Graves Disease 1 56 0.031
537
HPT022 Hepatoblastoma 56 0.031
538
c PRG126 Progressive Familial Heart Block 55 0.031
539
c BCT007 Bacterial Meningitis 55 0.031
540
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.031
541
NPH009 Nephrolithiasis 55 0.031
542
P DBT005 Diabetes Insipidus 55 0.031
543
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.031
544
HYP060 Hyperinsulinism 54 0.031
545
GST037 Gastroparesis 54 0.031
546
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.031
547
AMN001 Amenorrhea 54 0.031
548
P END047 Endophthalmitis 53 0.031
549
P EPD016 Epidermolysis Bullosa 53 0.031
550
P PLM006 Pulmonary Alveolar Proteinosis 53 0.031
551
P RTN018 Retinal Disease 53 0.031
552
c CNT035 Central Nervous System Disease 52 0.031
553
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.031
554
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
555
P DDN001 Duodenal Ulcer 52 0.031
556
THY030 Thyroid Gland Disease 52 0.031
557
P NRC002 Narcolepsy 52 0.031
558
HYP014 Hyperuricemia 52 0.031
559
P TRT010 Teratoma 52 0.031
560
c ACT078 Acute Porphyria 51 0.031
561
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.031
562
P ECL001 Eclampsia 50 0.031
563
P MTR003 Mitral Valve Stenosis 50 0.031
564
OPT003 Opiate Dependence 50 0.031
565
P ART018 Aortic Valve Insufficiency 49 0.031
566
XNT003 Xanthomatosis 49 0.031
567
LRN003 Learning Disability 49 0.031
568
c MTR002 Mitral Valve Insufficiency 48 0.031
569
c HYD064 Hydrocephalus, Congenital, 1 48 0.031
570
PYL006 Pyloric Stenosis 48 0.031
571
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.031
572
SRT004 Serotonin Syndrome 47 0.031
573
c PRM093 Premature Ovarian Failure 7 47 0.031
574
RYN005 Raynaud Phenomenon 47 0.031
575
ATN005 Autonomic Dysfunction 46 0.031
576
MTS001 Mutism 46 0.031
577
SPN020 Spondylosis 46 0.031
578
HYD005 Hydrocele 46 0.031
579
c MLG068 Malignant Glioma 46 0.031
580
MXD026 Mixed Glioma 45 0.031
581
URT010 Ureteral Obstruction 45 0.031
582
P OCY003 Oocyte Maturation Defect 1 45 0.031
583
ATN004 Autonomic Neuropathy 45 0.031
584
IMM064 Immunodeficiency, Common Variable, 10 44 0.031
585
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.031
586
PRN021 Paranasal Sinus Disease 44 0.031
587
c FML036 Familial Periodic Paralysis 44 0.031
588
SPN369 Spinal Disease 43 0.031
589
BLD063 Bile Duct Cysts 43 0.031
590
c SRC023 Sarcoidosis 2 43 0.031
591
MDD018 Middle East Respiratory Syndrome 43 0.031
592
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.031
593
ORL015 Oral Squamous Cell Carcinoma 43 0.031
594
ORB013 Orbital Disease 42 0.031
595
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.031
596
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.031
597
PRS063 Paresthesia 41 0.031
598
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.031
599
P HYP009 Hypertrophic Pyloric Stenosis 41 0.031
600
MLR006 Male Reproductive Organ Cancer 40 0.031
601
HYP540 Hypertension, Diastolic 40 0.031
602
ART008 Arteriosclerosis Obliterans 40 0.031
603
MLG086 Malignant Hyperthermia Susceptibility 39 0.031
604
c PLY105 Polycystic Ovary Syndrome 1 38 0.031
605
c OVR114 Ovarian Cancer 1 38 0.031
606
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.031
607
P HMF004 Hemifacial Spasm 38 0.031
608
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.031
609
CRT012 Cortical Blindness 37 0.031
610
FST001 Foster-Kennedy Syndrome 36 0.031
611
CMP006 Complex Partial Epilepsy 36 0.031
612
c ACT036 Acute Cholangitis 36 0.031
613
ACL001 Acalculous Cholecystitis 35 0.031
614
FXD003 Fixed Drug Eruption 35 0.031
615
CRB079 Cerebrospinal Fluid Leak 35 0.031
616
CRV025 Cervical Incompetence 34 0.031
617
PLM028 Pulmonary Coin Lesion 33 0.031
618
GGN002 Gigantism 33 0.031
619
c PRG106 Progressive Muscular Dystrophy 33 0.031
620
BNN005 Bunion 33 0.031
621
CRB031 Cerebral Arterial Disease 33 0.031
622
c HMF011 Hemifacial Spasm, Familial 33 0.031
623
TTH030 Teeth, Supernumerary 33 0.031
624
OVR109 Ovarian Germ Cell Teratoma 32 0.031
625
c ALC016 Alcohol Sensitivity, Acute 31 0.031
626
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.031
629
TRT017 Teratoma, Ovarian 29 0.031
630
ANS021 Anisocoria 27 0.031
631
ADT002 Auditory System Cancer 26 0.031
632
FNC005 Functional Colonic Disease 26 0.031
633
HRP008 Herpes Simiae 25 0.031
634
ATR089 Atrioventricular Dissociation 20 0.031
635
LWF001 Low-Flow Priapism 19 0.031
636
c FML159 Familial Periodic Paralyses 16 0.031
637
c SYS001 Systemic Lupus Erythematosus 86 0.022
639
c LKM061 Leukemia, Acute Myeloid 84 0.022
640
MLR004 Malaria 81 0.022
641
CYS001 Cystic Fibrosis 81 0.022
642
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.022
643
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.022
644
PHN003 Phenylketonuria 75 0.022
645
ADR007 Adrenoleukodystrophy 75 0.022
646
END057 Endometrial Cancer 74 0.022
647
c BTT014 Beta-Thalassemia 74 0.022
648
c MNN043 Meningioma, Familial 74 0.022
649
c HYP836 Hypercholesterolemia, Familial, 1 73 0.022
650
ULC004 Ulcerative Colitis 73 0.022
651
P RTN024 Retinoblastoma 73 0.022
652
BRT054 Brittle Bone Disorder 72 0.022
653
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.022
654
P JBR020 Joubert Syndrome 1 72 0.022
655
P MLT020 Multiple Sclerosis 72 0.022
656
c HPT073 Hepatitis C Virus 72 0.022
657
P GRF003 Graft-Versus-Host Disease 72 0.022
658
c LKM063 Leukemia, Chronic Myeloid 72 0.022
659
HMN044 Human Immunodeficiency Virus Type 1 71 0.022
660
P AMY004 Amyloidosis 70 0.022
661
MYL009 Myelodysplastic Syndrome 70 0.022
662
c PNC108 Pancreatitis, Hereditary 70 0.022
663
P MLN008 Melanoma 69 0.022
664
SVR097 Severe Cutaneous Adverse Reaction 69 0.022
665
LYM133 Lymphoma, Hodgkin, Classic 69 0.022
666
P LPR021 Leprosy 3 69 0.022
667
SKN019 Skin Melanoma 68 0.022
668
PNC129 Pancreatic Adenocarcinoma 68 0.022
669
c INF071 Inflammatory Bowel Disease 1 67 0.022
670
P TRC072 Treacher Collins Syndrome 1 66 0.022
671
P SKN015 Skin Carcinoma 66 0.022
672
P NSP012 Nasopharyngeal Carcinoma 66 0.022
673
P DRM053 Dermatitis, Atopic 66 0.022
674
P PLM036 Pulmonary Fibrosis 65 0.022
675
P CNJ013 Conjunctivitis 65 0.022
676
P LPS002 Liposarcoma 65 0.022
677
CHY002 Chylomicron Retention Disease 65 0.022
678
c DBT099 Diabetes Mellitus, Type I 65 0.022
679
CLN015 Colon Adenocarcinoma 65 0.022
680
P CHR071 Charcot-Marie-Tooth Disease 65 0.022
681
OVR029 Ovarian Hyperstimulation Syndrome 64 0.022
682
CLF027 Cleft Palate, Isolated 64 0.022
683
GT001 Gout 64 0.022
684
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.022
685
DGR001 Digeorge Syndrome 64 0.022
686
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.022
687
P RHB003 Rhabdomyosarcoma 63 0.022
688
PLG002 Plague 63 0.022
689
MSC152 Muscular Dystrophy, Becker Type 63 0.022
690
P DST002 Distal Arthrogryposis 63 0.022
691
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.022
692
ACT119 Acute Promyelocytic Leukemia 63 0.022
693
INT146 Intervertebral Disc Disease 63 0.022
694
P END044 Endometriosis 63 0.022
695
c GLC092 Glaucoma, Primary Open Angle 62 0.022
696
c ALP101 Alpha-Thalassemia 62 0.022
697
ERL001 Early Myoclonic Encephalopathy 62 0.022
698
LPD008 Lipid Metabolism Disorder 62 0.022
699
c HPT001 Hepatitis C 62 0.022
700
c BRN108 Branchiootic Syndrome 1 62 0.022
701
c SVR001 Severe Acute Respiratory Syndrome 62 0.022
702
P BCK002 Beckwith-Wiedemann Syndrome 62 0.022
703
LSC001 Lesch-Nyhan Syndrome 62 0.022
704
ATM095 Autoimmune Disease 62 0.022
705
BRS099 Breast Ductal Carcinoma 62 0.022
706
MNN042 Meningioma, Radiation-Induced 62 0.022
707
MDD011 Mood Disorder 62 0.022
708
P DRM010 Dermatomyositis 61 0.022
709
OST003 Osteonecrosis 61 0.022
710
ART141 Arteriovenous Malformations of the Brain 61 0.022
711
P LPS004 Lupus Erythematosus 61 0.022
712
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.022
713
CNT105 Central Core Disease of Muscle 60 0.022
714
P BNG030 Benign Ependymoma 60 0.022
715
P VNT002 Ventricular Septal Defect 60 0.022
716
ACQ007 Acquired Immunodeficiency Syndrome 60 0.022
717
LBR030 Leber Optic Atrophy 60 0.022
718
P PTN014 Patent Ductus Arteriosus 1 60 0.022
719
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.022
720
P THL005 Thalassemia 60 0.022
721
c HRD002 Hereditary Angioedema 60 0.022
722
P EPS003 Episodic Ataxia 59 0.022
723
P MCR010 Microcephaly 59 0.022
724
CHL014 Cholera 59 0.022
725
P BND020 Bone Disease 59 0.022
726
BRN002 Bronchiolitis 59 0.022
727
PPT005 Peptic Ulcer Disease 59 0.022
728
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 0.022
729
CHR072 Chordoma 58 0.022
730
c PRM005 Primary Hyperparathyroidism 58 0.022
731
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 0.022
732
BRS051 Breast Disease 58 0.022
733
ERY003 Erythema Multiforme 58 0.022
734
P GLL018 Gallbladder Cancer 57 0.022
735
P PLV020 Pelvic Organ Prolapse 57 0.022
736
c CHR417 Chronic Graft Versus Host Disease 57 0.022
737
IRN002 Iron Metabolism Disease 57 0.022
738
c VSC019 Vesicoureteral Reflux 1 57 0.022
739
BRD001 Brody Myopathy 57 0.022
740
P END033 Endocarditis 57 0.022
741
P PRV006 Pervasive Developmental Disorder 57 0.022
742
c ANG068 Angioedema, Hereditary, Type I 57 0.022
743
BLR008 Bilirubin Metabolic Disorder 57 0.022
744
GLT035 Glutaric Acidemia I 57 0.022
745
LNN001 Lennox-Gastaut Syndrome 57 0.022
746
PHR003 Pharyngitis 57 0.022
747
FRC011 Fructose Intolerance, Hereditary 57 0.022
748
P ANG015 Angioedema 57 0.022
749
BCT022 Bacterial Infectious Disease 56 0.022
750
ACS001 Acoustic Neuroma 56 0.022
751
P ISL078 Isolated Ectopia Lentis 56 0.022
752
c MCR256 Microphthalmia, Syndromic 9 56 0.022
753
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.022
754
P ATR001 Atrioventricular Septal Defect 55 0.022
755
HMF006 Hemifacial Microsomia 55 0.022
756
P MYP006 Myopia 55 0.022
757
CRC006 Carcinoid Syndrome 55 0.022
758
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.022
759
P LRY044 Larynx Cancer 55 0.022
760
GLS001 Gliosarcoma 54 0.022
761
GLC003 Glucose Intolerance 54 0.022
762
P CYS039 Cystic Kidney Disease 54 0.022
763
CLL010 Cellular Ependymoma 54 0.022
764
ANL018 Analbuminemia 54 0.022
765
HMS001 Hemosiderosis 54 0.022
766
HLL004 Hellp Syndrome 54 0.022
767
PPL022 Papilloma 54 0.022
768
CRH005 Crohn's Colitis 53 0.022
769
INF034 Infective Endocarditis 53 0.022
770
HYP063 Hypersplenism 53 0.022
771
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.022
772
c XNT010 Xanthinuria, Type I 53 0.022
773
P FBR031 Febrile Seizures 53 0.022
774
GST023 Gastric Ulcer 53 0.022
775
PRP080 Peripheral Artery Disease 53 0.022
776
c FML008 Familial Retinoblastoma 53 0.022
777
ALC009 Alcoholic Liver Cirrhosis 53 0.022
778
c FML191 Familial Long Qt Syndrome 53 0.022
779
CHR073 Choreatic Disease 52 0.022
780
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.022
781
IMP005 Impotence 52 0.022
782
PPT001 Peptic Esophagitis 52 0.022
783
TLN003 Telangiectasis 52 0.022
784
c ACT135 Acute Graft Versus Host Disease 52 0.022
785
P SPP010 Suppressor of Tumorigenicity 3 51 0.022
786
MCR088 Microscopic Polyangiitis 51 0.022
787
ALK024 Alkuraya-Kucinskas Syndrome 51 0.022
788
ANK001 Ankylosis 51 0.022
789
CLB002 Clubfoot 51 0.022
790
NRM004 Neuroma 51 0.022
791
SPN019 Spondylolisthesis 51 0.022
792
P AST007 Astrocytoma 51 0.022
793
c SCN007 Secondary Hyperparathyroidism 51 0.022
794
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.022
795
SKN013 Skin Benign Neoplasm 51 0.022
796
PNM005 Pneumonic Plague 51 0.022
797
INT071 Intestinal Perforation 51 0.022
798
CHR005 Chorioamnionitis 51 0.022
799
SCH012 Schizoaffective Disorder 50 0.022
800
PRT029 Parathyroid Adenoma 50 0.022
801
P OVR082 Overgrowth Syndrome 50 0.022
802
RDC002 Radiculopathy 50 0.022
803
SPN021 Spinal Meningioma 50 0.022
804
CRN030 Coronary Stenosis 50 0.022
805
CHL122 Cholesteatoma of Middle Ear 50 0.022
806
P PRS049 Persistent Mullerian Duct Syndrome 50 0.022
807
ALN001 Aland Island Eye Disease 50 0.022
808
P SCK005 Sickle Cell Disease 50 0.022
809
PRT018 Portal Vein Thrombosis 50 0.022
810
ECT026 Ectopic Pregnancy 50 0.022
811
NTR046 Neutrophil Migration 50 0.022
812
P MTH008 Methylmalonic Acidemia 50 0.022
813
HYP080 Hypogonadism 50 0.022
814
PPL021 Papilledema 49 0.022
815
P OPN001 Open-Angle Glaucoma 49 0.022
816
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.022
817
SBP001 Subependymal Giant Cell Astrocytoma 49 0.022
818
BNR002 Bone Resorption Disease 48 0.022
819
THY123 Thyroid Gland Follicular Carcinoma 48 0.022
820
SBS004 Substance Dependence 48 0.022
821
RGH001 Right Bundle Branch Block 48 0.022
822
DGN001 Degenerative Disc Disease 48 0.022
823
P HRD021 Hereditary Sensory Neuropathy 48 0.022
824
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.022
825
NNT017 Neonatal Adrenoleukodystrophy 47 0.022
826
RDT013 Radiation Proctitis 47 0.022
827
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.022
828
DRG003 Drug Dependence 47 0.022
829
LRY029 Laryngomalacia 47 0.022
830
PRC003 Proctitis 47 0.022
831
c INH020 Inherited Metabolic Disorder 47 0.022
832
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.022
833
P CRC039 Coarctation of Aorta 47 0.022
834
CNT033 Central Nervous System Cancer 47 0.022
835
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.022
836
CHR074 Choriocarcinoma 47 0.022
837
P OVR046 Ovarian Cyst 47 0.022
838
ASP004 Asphyxia Neonatorum 46 0.022
839
ALB002 Albinism 46 0.022
840
TST014 Testicular Cancer 46 0.022
841
TTH006 Tooth Disease 46 0.022
842
CMP034 Complete Androgen Insensitivity Syndrome 46 0.022
843
FCL012 Facial Paralysis 46 0.022
844
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.022
845
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.022
846
P HMR005 Hemorrhoid 46 0.022
847
CRN019 Coronary Artery Vasospasm 46 0.022
848
SQM002 Squamous Cell Papilloma 46 0.022
849
ANR004 Anuria 46 0.022
850
c TRC022 Tricuspid Valve Insufficiency 45 0.022
851
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.022
852
MCR037 Macroglossia 45 0.022
853
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.022
854
URL001 Urolithiasis 45 0.022
855
ACT003 Acute Kidney Tubular Necrosis 45 0.022
856
SPS007 Spastic Cerebral Palsy 45 0.022
857
MYF001 Myofibroma 45 0.022
858
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.022
859
CRD003 Cardiac Sarcoidosis 44 0.022
860
P MTC004 Mitochondrial Encephalomyopathy 44 0.022
861
THR012 Thoracic Cancer 44 0.022
862
P SYR001 Syringomyelia 44 0.022
863
CVD001 Covid-19 44 0.022
864
HMP009 Haemophilus Influenzae 43 0.022
865
PNM013 Pneumococcal Meningitis 42 0.022
866
P CLS010 Cluster Headache 42 0.022
867
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.022
868
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.022
869
RST023 Resting Heart Rate, Variation in 41 0.022
870
LMB024 Limbic Encephalitis 41 0.022
871
LCR013 Lacrimal Duct Defect 41 0.022
872
P RRH023 Rare Hereditary Hemochromatosis 41 0.022
873
EXT022 Exotropia 41 0.022
874
P SCL057 Scoliosis, Isolated 1 41 0.022
875
KLB003 Klebsiella Pneumonia 41 0.022
876
SCR001 Secretory Meningioma 41 0.022
877
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.022
878
MCL003 Macular Holes 40 0.022
879
ART103 Arthrogryposis, Mental Retardation, and Seizures 40 0.022
880
TBL003 Tubular Adenocarcinoma 40 0.022
881
ALC005 Alcoholic Pancreatitis 40 0.022
882
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.022
883
CRD005 Cardia Cancer 40 0.022
884
PLC009 Placenta Praevia 39 0.022
885
SPS004 Spastic Quadriplegia 39 0.022
886
RTC012 Reticuloendotheliosis, X-Linked 39 0.022
887
VTR003 Vitreous Detachment 39 0.022
888
DSS010 Dissociative Disorder 39 0.022
889
RTN002 Retinal Perforation 38 0.022
890
CHL039 Choledocholithiasis 38 0.022
891
ALL014 Allergic Encephalomyelitis 38 0.022
892
P PRC031 Preeclampsia/eclampsia 1 38 0.022
893
ADR022 Adrenomyeloneuropathy 38 0.022
894
HYP264 Hypertonia 38 0.022
895
c MLG157 Malignant Pheochromocytoma 38 0.022
896
ALG027 Al-Gazali-Bakalinova Syndrome 38 0.022
897
OVR094 Ovarian Epithelial Cancer 38 0.022
898
LNS001 Lens Subluxation 38 0.022
899
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.022
900
SWL001 Swallowing Disorders 38 0.022
901
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.022
902
P FML187 Familial Hypertension 37 0.022
903
PRR004 Preretinal Fibrosis 37 0.022
904
SYR010 Syringomyelia, Noncommunicating Isolated 37 0.022
905
HRN029 Hearing Loss, Noise-Induced 37 0.022
906
P HRD217 Hereditary Optic Neuropathy 36 0.022
907
ABD010 Abdominal Wall Defect 36 0.022
908
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.022
909
PLM011 Plummer's Disease 35 0.022
910
SCN049 Second-Degree Atrioventricular Block 35 0.022
911
FST010 Fasting Hypoglycemia 35 0.022
912
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.022
913
HNS001 Hansen's Disease 34 0.022
914
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.022
915
ALT003 Alternating Exotropia 34 0.022
916
CRT008 Carotid Artery Dissection 33 0.022
917
PPL052 Papillomatosis, Confluent and Reticulated 33 0.022
918
c SCH085 Schizophrenia 2 33 0.022
919
HND015 Hand Skill, Relative 33 0.022
920
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.022
921
c CLR079 Colorectal Cancer 2 32 0.022
922
PRX097 Paroxysmal Dystonia 32 0.022
923
THY001 Thyroid Crisis 31 0.022
924
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.022
925
c PRG019 Paragangliomas 2 31 0.022
926
MLT116 Multiple System Atrophy, Parkinsonian Type 30 0.022
927
ERY066 Erythema Multiforme Major 30 0.022
928
VRT001 Vertebral Artery Occlusion 30 0.022
929
CVR010 Cavernous Malformation 30 0.022
930
BSL004 Basilar Artery Occlusion 29 0.022
931
LGM010 Legume Allergy 29 0.022
932
ISL099 Isolated Methylmalonic Acidemia 29 0.022
933
CRB029 Cerebellopontine Angle Tumor 29 0.022
934
DSR074 Disorder of Purine Metabolism 29 0.022
935
PST092 Posttransplant Acute Limbic Encephalitis 29 0.022
936
P PPL023 Pupil Disease 28 0.022
937
IMM162 Immunoglobulin E Concentration, Serum 28 0.022
938
P PRG139 Progeroid Syndrome 28 0.022
939
CRN051 Craniofacial Microsomia 28 0.022
940
CNG506 Congenital Amyoplasia 27 0.022
941
ARG004 Argyria 27 0.022
942
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.022
943
STR033 Storm Syndrome 26 0.022
944
BNG077 Benign Idiopathic Neonatal Seizures 26 0.022
945
EXP002 Exposure Keratitis 26 0.022
946
ACT162 Acute Sensory Ataxic Neuropathy 26 0.022
947
PRQ002 Paraquat Poisoning 26 0.022
948
P FRT001 Fourth Cranial Nerve Palsy 26 0.022
949
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.022
950
P PLM064 Pulmonary Sequestration 22 0.022
951
JMP002 Jumping Frenchmen of Maine 22 0.022
952
RDL001 Radial Nerve Lesion 20 0.022
953
EPL170 Epilepsy-Aphasia Spectrum 20 0.022
954
CD4008 Cd4/cd8 T-Cell Ratio 20 0.022
955
TMP006 Temporomandibular Ankylosis 20 0.022
956
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.022
957
INH017 Inherited Congenital Spastic Tetraplegia 18 0.022
958
VNT036 Ventilator-Induced Diaphragmatic Dysfunction 17 0.022
959
CNG491 Congenital Portosystemic Shunt 17 0.022
960
c RNL034 Renal Cell Carcinoma 4 16 0.022
961
CHS007 Chester Porphyria 15 0.022
962
P INT320 Intelligence Quantitative Trait Locus 1 15 0.022
Content
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