Search results for Anesthetics

2959 hits were found for Anesthetics

# Family MCID Name MIFTS Score
1
c MLG147 Malignant Hyperthermia 1 43 2.905
2
PNG002 Pain Agnosia 51 0.310
3
P CRD119 Cardiac Arrest 67 0.161
4
P MLG056 Malignant Hyperthermia 67 0.146
5
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.146
6
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.145
7
c PNS012 Paine Syndrome 61 0.143
8
HYP266 Hypoxia 57 0.133
9
P PHC003 Pheochromocytoma 71 0.131
10
ADR040 Adrenal Gland Pheochromocytoma 46 0.131
11
P PLM037 Pulmonary Hypertension 67 0.122
12
P CHR345 Chronic Pain 44 0.122
13
ISC004 Ischemia 58 0.115
14
P RSP003 Respiratory Failure 74 0.113
15
PNM008 Pneumothorax 56 0.112
16
P SLP006 Sleep Apnea 69 0.108
17
PLP001 Pulpitis 49 0.108
18
c ATR087 Atrial Standstill 1 75 0.106
19
AMN003 Amnestic Disorder 54 0.106
20
PLM010 Pulmonary Edema 54 0.104
21
SBC016 Subacute Delirium 44 0.104
22
ANR040 Aneurysm 59 0.100
23
HRT011 Heart Septal Defect 50 0.100
24
ING001 Inguinal Hernia 60 0.099
25
P HRT032 Heart Disease 75 0.097
26
P SCL018 Scoliosis 60 0.097
27
48X005 48,xyyy 39 0.097
28
CNG034 Congestive Heart Failure 69 0.096
29
ALL026 Allergic Hypersensitivity Disease 62 0.095
30
P MTH007 Methemoglobinemia 46 0.094
31
P SZR006 Seizure Disorder 56 0.094
32
P MYP004 Myopathy 70 0.093
33
P CTR002 Cataract 60 0.091
34
HYP056 Hypoglycemia 66 0.090
35
ANX010 Anxiety 73 0.089
36
VSL002 Visual Epilepsy 59 0.089
37
P STR020 Strabismus 55 0.087
38
MCH006 Mechanical Strabismus 42 0.087
39
ATR057 Atrioventricular Block 55 0.087
40
MTB004 Metabolic Acidosis 50 0.087
41
P KDN018 Kidney Disease 72 0.083
42
ART016 Aortic Aneurysm 69 0.082
43
CYN002 Cyanosis, Transient Neonatal 45 0.082
44
SPN186 Spinal Cord Injury 60 0.082
45
c DLT002 Dilated Cardiomyopathy 79 0.081
46
c PRC016 Pre-Eclampsia 63 0.080
47
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.078
48
P VNT002 Ventricular Septal Defect 60 0.077
49
c ACT071 Acute Kidney Failure 60 0.077
50
LNG099 Lung Disease 60 0.076
51
P EPD016 Epidermolysis Bullosa 53 0.076
52
HLX001 Helix Syndrome 47 0.076
53
P TTR001 Tetralogy of Fallot 70 0.075
54
P HDC001 Headache 57 0.074
55
OCL069 Ocular Motor Apraxia 51 0.074
56
BCK006 Back Pain 42 0.074
57
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.073
58
LPT014 Leptin Deficiency or Dysfunction 74 0.073
59
LPP008 Lipoprotein Quantitative Trait Locus 62 0.073
60
STT001 Status Epilepticus 60 0.073
61
PLM033 Pulmonary Embolism 59 0.073
62
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.073
63
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.073
64
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.073
65
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.073
66
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.073
67
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.073
68
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.073
69
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.073
70
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.073
71
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.073
72
P ALZ034 Alzheimer Disease 88 0.072
73
P MYS003 Myasthenia Gravis 68 0.072
74
DPR016 Depression 63 0.072
75
HYP066 Hyperglycemia 61 0.072
76
ATX019 Ataxia with Vitamin E Deficiency 42 0.072
77
P ATR010 Atrial Heart Septal Defect 60 0.071
78
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.070
79
P THR014 Thrombocytopenia 67 0.070
80
P MSC005 Muscular Dystrophy 66 0.070
81
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.070
82
47X002 47,xyy 49 0.070
83
P ART005 Arteriovenous Malformation 65 0.069
84
c FNC043 Fanconi Anemia, Complementation Group E 62 0.069
85
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.069
86
ART140 Arteries, Anomalies of 52 0.069
87
OST012 Osteoarthritis 78 0.068
88
c THR092 Thrombophilia Due to Thrombin Defect 73 0.068
89
GST092 Gastroesophageal Reflux 67 0.068
90
KRT019 Keratitis, Hereditary 65 0.068
91
TXC005 Toxic Shock Syndrome 62 0.067
92
ILS001 Ileus 51 0.067
93
P ECL001 Eclampsia 50 0.067
94
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.067
95
P HYP265 Hypotonia 43 0.067
96
P TRM003 Tremor 54 0.066
97
CLF001 Cleft Lip 53 0.066
98
P PRP029 Porphyria 62 0.065
99
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.065
100
P VSC007 Vascular Disease 63 0.064
101
BRN071 Brain Injury 49 0.064
102
SYN036 Syncope 45 0.064
103
TRC005 Tracheal Stenosis 38 0.064
104
INT075 Intracranial Hypertension 53 0.063
105
P MYT002 Myotonic Dystrophy 49 0.063
106
P HYP061 Hypertrophic Cardiomyopathy 70 0.062
107
ANG054 Angina Pectoris 66 0.062
108
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.062
109
CMP010 Complex Regional Pain Syndrome 58 0.062
110
P URT039 Urticaria 58 0.062
111
P NRP001 Neuropathy 56 0.062
112
CVD001 Covid-19 44 0.062
113
P NRB001 Neuroblastoma 72 0.061
114
DFC004 Deficiency Anemia 70 0.061
115
CRB039 Cerebrovascular Disease 67 0.061
116
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.061
117
P HYD006 Hydrocephalus 66 0.061
118
LVR012 Liver Cirrhosis 62 0.061
119
HYP005 Hypokalemia 55 0.061
120
DYS073 Dysphagia 50 0.061
121
ATS010 Autosomal Recessive Disease 48 0.061
122
c MTR002 Mitral Valve Insufficiency 48 0.061
123
PRS063 Paresthesia 41 0.061
124
CHL079 Children's Interstitial Lung Disease 26 0.061
125
P CLR023 Colorectal Cancer 99 0.060
126
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.060
127
P HMN010 Hemangioma 61 0.060
128
ANX004 Anoxia 40 0.060
129
SNG003 Single Ventricular Heart 30 0.060
130
CRB037 Cerebral Palsy 69 0.058
131
P ATR011 Atrial Fibrillation 66 0.058
132
TTN003 Tetanus 65 0.058
133
CLF027 Cleft Palate, Isolated 64 0.058
134
MNT002 Mental Depression 58 0.058
135
HRT012 Heart Valve Disease 53 0.058
136
TRM010 Traumatic Brain Injury 51 0.058
137
END086 End Stage Renal Disease 51 0.058
138
ASP007 Aspiration Pneumonia 48 0.058
139
ENT001 Enterocele 39 0.058
140
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.057
141
P TRN020 Turner Syndrome 67 0.057
142
P LNG028 Long Qt Syndrome 66 0.057
143
P CRN300 Coronary Heart Disease 1 63 0.057
144
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.057
145
P HRN001 Horner's Syndrome 45 0.057
146
STR067 Stroke, Ischemic 81 0.056
147
P HYP086 Hypothyroidism 69 0.056
148
APN008 Apnea, Obstructive Sleep 64 0.056
149
P ART023 Arthropathy 62 0.056
150
P ENC018 Encephalopathy 61 0.056
151
P MYM013 Moyamoya Disease 1 57 0.056
152
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.056
153
ESP021 Esophageal Cancer 90 0.055
154
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.055
155
c MGR028 Migraine with or Without Aura 1 67 0.055
156
P DYS154 Dystonia 65 0.055
157
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.055
158
P PTN014 Patent Ductus Arteriosus 1 60 0.055
159
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.055
160
P SBS003 Substance Abuse 55 0.055
161
P LTR001 Lateral Sclerosis 54 0.055
162
CRB086 Cerebral Aneurysms 40 0.055
163
P MLT020 Multiple Sclerosis 72 0.053
164
DRM006 Dermatitis 61 0.053
165
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.053
166
PRP016 Paraplegia 52 0.053
167
PTH003 Pathologic Nystagmus 52 0.053
168
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.053
169
CRB004 Cerebral Artery Occlusion 45 0.053
170
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.053
171
P BRS047 Breast Cancer 97 0.052
172
c HYP595 Hypertension, Essential 84 0.052
173
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.052
174
BRT054 Brittle Bone Disorder 72 0.052
175
P BRG001 Brugada Syndrome 71 0.052
176
P EPL164 Epilepsy 71 0.052
177
P ADL010 Adult Respiratory Distress Syndrome 65 0.052
178
P PRD008 Periodontitis 64 0.052
179
c SVR001 Severe Acute Respiratory Syndrome 62 0.052
180
ESP020 Esophageal Atresia 62 0.052
181
APP008 Appendicitis 61 0.052
182
CRD223 Cardiac Arrhythmia 60 0.052
183
PRT013 Portal Hypertension 59 0.052
184
c ACT075 Acute Myocardial Infarction 57 0.052
185
P HYP076 Hyperthyroidism 55 0.052
186
P PTS002 Ptosis 53 0.052
187
P PRG013 Paraganglioma 52 0.052
188
ART074 Aortic Dissection 52 0.052
189
PCT003 Pectus Excavatum 49 0.052
190
ATN005 Autonomic Dysfunction 46 0.052
191
TTH006 Tooth Disease 46 0.052
192
c TRC022 Tricuspid Valve Insufficiency 45 0.052
193
DRG024 Drug Allergy 42 0.052
194
P HPT023 Hepatocellular Carcinoma 100 0.051
195
P CNR004 Cone-Rod Dystrophy 2 73 0.051
196
DWN001 Down Syndrome 70 0.051
197
P LVR013 Liver Disease 68 0.051
198
PNM010 Pneumothorax, Primary Spontaneous 60 0.051
199
ADN018 Adenoma 59 0.051
200
AGN016 Aging 56 0.051
201
CLF004 Cleft Lip/palate 54 0.051
202
HYP060 Hyperinsulinism 54 0.051
203
P HMP007 Hemophilia 51 0.051
204
P LCT001 Lactic Acidosis 51 0.051
205
P MTR003 Mitral Valve Stenosis 50 0.051
206
KRT008 Keratopathy 47 0.051
207
HDN002 Head Injury 46 0.051
208
PLC009 Placenta Praevia 39 0.051
209
P MYC007 Myocardial Infarction 70 0.049
210
ADL002 Adult Syndrome 70 0.049
211
P DMN002 Dementia 66 0.049
212
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.049
213
PRT036 Peritonitis 64 0.049
214
NRM005 Neuromuscular Disease 64 0.049
215
TRG002 Trigeminal Neuralgia 60 0.049
216
c ACT027 Acute Pancreatitis 60 0.049
217
P SLP005 Sleep Disorder 59 0.049
218
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.049
219
INT030 Intracranial Aneurysm 56 0.049
220
PRP030 Purpura 54 0.049
221
P MSC003 Muscular Atrophy 52 0.049
222
c SVR005 Severe Pre-Eclampsia 50 0.049
223
CRT015 Carotid Artery Occlusion 45 0.049
224
PST053 Postherpetic Neuralgia 40 0.049
225
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.048
226
P CHR071 Charcot-Marie-Tooth Disease 65 0.048
227
c BRN108 Branchiootic Syndrome 1 62 0.048
228
VRC005 Varicose Veins 60 0.048
229
P ANG015 Angioedema 57 0.048
230
CRC006 Carcinoid Syndrome 55 0.048
231
HLL004 Hellp Syndrome 54 0.048
232
STT002 Status Asthmaticus 50 0.048
233
P ART018 Aortic Valve Insufficiency 49 0.048
234
CHL004 Cholelithiasis 49 0.048
235
P CRC039 Coarctation of Aorta 47 0.048
236
PTT037 Pituitary Tumors 44 0.048
237
DWR001 Dwarfism 44 0.048
238
MSC157 Muscular Dystrophy, Duchenne Type 72 0.046
239
HMN044 Human Immunodeficiency Virus Type 1 71 0.046
240
c CHR684 Chronic Kidney Disease 70 0.046
241
c ART101 Aortic Valve Disease 2 65 0.046
242
P DBT009 Diabetes Mellitus 64 0.046
243
P MST009 Mastocytosis 64 0.046
244
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.046
245
P INT143 Interstitial Cystitis 61 0.046
246
P PNC044 Pancreatitis 61 0.046
247
P CYS018 Cystitis 59 0.046
248
CRD132 Cardiac Conduction Defect 58 0.046
249
CNT047 Contact Dermatitis 58 0.046
250
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.046
251
P EHL001 Ehlers-Danlos Syndrome 58 0.046
252
RFL001 Reflex Sympathetic Dystrophy 54 0.046
253
P RCT021 Rectum Cancer 52 0.046
254
P TRT010 Teratoma 52 0.046
255
CRN030 Coronary Stenosis 50 0.046
256
CRT013 Carotid Stenosis 50 0.046
257
P SCK005 Sickle Cell Disease 50 0.046
258
LRN003 Learning Disability 49 0.046
259
PLC007 Placental Abruption 48 0.046
260
ANH002 Anhidrosis 47 0.046
261
PLC001 Placenta Accreta 46 0.046
262
LWC001 Low Compliance Bladder 43 0.046
263
CYT002 Cytokine Deficiency 42 0.046
264
P PRS040 Prostate Cancer 97 0.045
265
c SPN225 Spondyloarthropathy 1 73 0.045
266
P ART022 Arthritis 69 0.045
267
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.045
268
P CRN037 Craniosynostosis 68 0.045
269
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.045
270
P HYP055 Hypoplastic Left Heart Syndrome 63 0.045
271
P LPS004 Lupus Erythematosus 61 0.045
272
HRP004 Herpes Zoster 60 0.045
273
ACQ007 Acquired Immunodeficiency Syndrome 60 0.045
274
INS001 Insulinoma 60 0.045
275
SPN027 Spinal Stenosis 59 0.045
276
THR024 Thrombosis 57 0.045
277
P MTC069 Mitochondrial Disorders 56 0.045
278
PRS045 Prostatic Hypertrophy 53 0.045
279
TXC002 Toxic Encephalopathy 53 0.045
280
RDC002 Radiculopathy 50 0.045
281
BLR001 Biliary Atresia 50 0.045
282
MYC005 Myocardial Stunning 46 0.045
283
P MYC033 Myoclonus 46 0.045
284
MCR037 Macroglossia 45 0.045
285
SPS057 Spasticity 45 0.045
286
MYF002 Myofascial Pain Syndrome 42 0.045
287
ALG001 Algoneurodystrophy 39 0.045
288
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.045
289
P PNC035 Pancreatic Cancer 84 0.043
290
IMM167 Immune Deficiency Disease 78 0.043
291
P PRK057 Parkinson Disease, Late-Onset 78 0.043
292
PSY004 Psychotic Disorder 67 0.043
293
PRT037 Pertussis 65 0.043
294
NRF007 Neurofibroma 64 0.043
295
P MVM001 Movement Disease 63 0.043
296
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.043
297
P OPT006 Optic Nerve Disease 60 0.043
298
PRT058 Pure Autonomic Failure 59 0.043
299
FBR047 Fibromyalgia 58 0.043
300
CNS004 Constipation 58 0.043
301
P PRP019 Peripheral Nervous System Disease 58 0.043
302
c ART061 Arthrogryposis, Distal, Type 2a 57 0.043
303
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.043
304
P PLY018 Polycythemia 56 0.043
305
P NRF002 Neurofibromatosis 56 0.043
306
P SCK002 Sick Sinus Syndrome 55 0.043
307
P DBT005 Diabetes Insipidus 55 0.043
308
P ART021 Arteriosclerosis 54 0.043
309
PRS021 Prostatic Adenoma 51 0.043
310
P MTC133 Mitochondrial Myopathy 49 0.043
311
PRS129 Prostatic Hyperplasia, Benign 49 0.043
312
CRD001 Cardiac Tamponade 47 0.043
313
UMB002 Umbilical Hernia 46 0.043
314
P HMR005 Hemorrhoid 46 0.043
315
IDP070 Idiopathic Scoliosis 42 0.043
316
CDQ001 Cauda Equina Syndrome 38 0.043
317
PLY150 Polykaryocytosis Inducer 31 0.043
318
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.043
319
P RHM011 Rheumatoid Arthritis 80 0.041
320
SCK003 Sickle Cell Anemia 74 0.041
321
OTT002 Otitis Media 72 0.041
322
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.041
323
WLF001 Wolff-Parkinson-White Syndrome 66 0.041
324
P NRV007 Nervous System Disease 66 0.041
325
KHL003 Kohlschutter-Tonz Syndrome 65 0.041
326
PRP083 Porphyria, Acute Intermittent 64 0.041
327
P GLM045 Glioma 63 0.041
328
c ACT068 Acute Cystitis 63 0.041
329
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.041
330
P BCK002 Beckwith-Wiedemann Syndrome 62 0.041
331
CHL068 Cholestasis 61 0.041
332
RTN017 Retinal Detachment 61 0.041
333
P MCR010 Microcephaly 59 0.041
334
P MTR012 Mitral Valve Disease 58 0.041
335
P EXN002 Exanthem 57 0.041
336
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.041
337
BRN004 Brain Edema 56 0.041
338
P GST044 Gastritis 56 0.041
339
DNT012 Dental Caries 53 0.041
340
SPN051 Spondylitis 51 0.041
341
BHR001 Behr Syndrome 51 0.041
342
MTC005 Mitochondrial Metabolism Disease 49 0.041
343
RYN005 Raynaud Phenomenon 47 0.041
344
GLL048 Glial Tumor 45 0.041
345
ATN004 Autonomic Neuropathy 45 0.041
346
MCP033 Mucopolysaccharidoses 38 0.041
347
CHR178 Chromosomal Triplication 35 0.041
348
HNS001 Hansen's Disease 34 0.041
350
BNN005 Bunion 33 0.041
351
INF009 Inflammatory Spondylopathy 31 0.041
352
P OVR042 Ovarian Cancer 88 0.039
353
c SYS001 Systemic Lupus Erythematosus 86 0.039
354
P GST053 Gastric Cancer 83 0.039
355
CYS001 Cystic Fibrosis 81 0.039
356
P BLD134 Bladder Cancer 79 0.039
357
c EXD008 Exudative Vitreoretinopathy 1 71 0.039
358
PRP027 Peripheral Vascular Disease 71 0.039
359
P AMY004 Amyloidosis 70 0.039
360
BRN024 Bronchitis 68 0.039
361
CRP001 Carpal Tunnel Syndrome 67 0.039
362
P NTR004 Neutropenia 63 0.039
363
P HYP069 Hyperparathyroidism 63 0.039
364
ATM095 Autoimmune Disease 62 0.039
365
P ENC004 Encephalitis 61 0.039
366
c WLM018 Wilms Tumor 5 61 0.039
367
STF001 Stiff-Person Syndrome 60 0.039
368
P BRN022 Bronchiectasis 59 0.039
369
THY029 Thyroid Carcinoma 59 0.039
370
IGR001 Ige Responsiveness, Atopic 59 0.039
371
DSS008 Disease of Mental Health 58 0.039
372
P GLL020 Gallbladder Disease 57 0.039
373
DSS009 Disseminated Intravascular Coagulation 57 0.039
374
P END033 Endocarditis 57 0.039
375
AYM001 Ayme-Gripp Syndrome 57 0.039
376
P MLT074 Multiple Endocrine Neoplasia 56 0.039
377
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.039
378
INT007 Intermediate Coronary Syndrome 55 0.039
379
FRZ001 Frozen Shoulder 53 0.039
380
c GLL024 Gallbladder Disease 1 53 0.039
381
TLN003 Telangiectasis 52 0.039
382
LMY002 Leiomyoma 52 0.039
383
ALK024 Alkuraya-Kucinskas Syndrome 51 0.039
384
ANK001 Ankylosis 51 0.039
385
CRD137 Cardiogenic Shock 47 0.039
386
P BNG032 Benign Mesothelioma 46 0.039
387
P KLP003 Klippel-Feil Syndrome 46 0.039
388
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.039
389
P CLS010 Cluster Headache 42 0.039
390
MYT011 Myotonia 34 0.039
391
CNG506 Congenital Amyoplasia 27 0.039
392
NRL016 Neural Tube Defects 82 0.038
393
P RTT002 Rett Syndrome 80 0.038
394
MRF001 Marfan Syndrome 77 0.038
395
AST005 Asthma 76 0.038
396
P SCH015 Schizophrenia 74 0.038
397
c MNN043 Meningioma, Familial 74 0.038
398
P LPR021 Leprosy 3 69 0.038
399
c HMP029 Hemophilia a 67 0.038
400
PPL049 Papillon-Lefevre Syndrome 65 0.038
401
P CRN015 Cornelia De Lange Syndrome 64 0.038
402
SKN016 Skin Disease 63 0.038
403
MNN042 Meningioma, Radiation-Induced 62 0.038
404
FTT001 Fatty Liver Disease 61 0.038
405
PST028 Post-Traumatic Stress Disorder 58 0.038
406
NWB001 Newborn Respiratory Distress Syndrome 58 0.038
407
P INF032 Infertility 57 0.038
408
CHL067 Cholecystitis 57 0.038
409
c CRN139 Cornelia De Lange Syndrome 1 57 0.038
410
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.038
411
P BPL003 Bipolar Disorder 56 0.038
412
HMP005 Hemiplegia 55 0.038
413
DBT010 Diabetic Neuropathy 54 0.038
414
CLL003 Cellulitis 54 0.038
415
INF034 Infective Endocarditis 53 0.038
416
IMP005 Impotence 52 0.038
417
ACH005 Achalasia 51 0.038
418
P HYP040 Hypospadias 51 0.038
419
SPN021 Spinal Meningioma 50 0.038
420
P CMP008 Compartment Syndrome 49 0.038
421
QDR001 Quadriplegia 48 0.038
422
P RNV001 Renovascular Hypertension 48 0.038
423
LPT006 Leptin Receptor Deficiency 48 0.038
424
SXL003 Sexual Disorder 47 0.038
425
HRN026 Hernia, Hiatus 47 0.038
426
ACT084 Acute Stress Disorder 47 0.038
427
P MTC004 Mitochondrial Encephalomyopathy 44 0.038
428
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.038
429
CRB090 Cerebral Hypoxia 44 0.038
430
GST020 Gastric Antral Vascular Ectasia 41 0.038
431
c MJR024 Major Affective Disorder 9 41 0.038
432
SCR001 Secretory Meningioma 41 0.038
433
P INT260 Intracranial Berry Aneurysm 39 0.038
434
c MJR022 Major Affective Disorder 8 38 0.038
435
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.038
436
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.038
437
DBL004 Double Discordia 23 0.038
438
CRH001 Crohn's Disease 74 0.036
439
PLY001 Polycythemia Vera 69 0.036
440
P MLN008 Melanoma 69 0.036
441
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.036
442
MST024 Mastocytosis, Cutaneous 69 0.036
443
P LYM118 Lymphoma 68 0.036
444
P PNM007 Pneumonia 68 0.036
445
P SYS005 Systemic Scleroderma 68 0.036
446
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.036
447
P HPT021 Hepatitis 67 0.036
448
ALC007 Alcohol Dependence 66 0.036
449
P PLM036 Pulmonary Fibrosis 65 0.036
450
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.036
451
PRP001 Propionic Acidemia 65 0.036
452
P HRP006 Herpes Simplex 65 0.036
453
P THY023 Thymoma 65 0.036
454
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.036
455
P SPN046 Spinal Muscular Atrophy 62 0.036
456
P LRS001 Larsen Syndrome 62 0.036
457
P ESP024 Esophagitis 62 0.036
458
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.036
459
c SCL052 Scleroderma, Familial Progressive 61 0.036
460
P SNS001 Sensorineural Hearing Loss 60 0.036
461
P PRD006 Prader-Willi Syndrome 59 0.036
462
P INT070 Intestinal Obstruction 58 0.036
463
CMM005 Common Cold 57 0.036
464
PHR003 Pharyngitis 57 0.036
465
c ACT134 Acute Liver Failure 56 0.036
466
MCS002 Mucositis 56 0.036
467
P PLY019 Polyneuropathy 56 0.036
468
NPH009 Nephrolithiasis 55 0.036
469
P MYP006 Myopia 55 0.036
470
P PTT006 Pituitary Adenoma 55 0.036
471
ESN011 Eisenmenger Syndrome 55 0.036
472
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.036
473
CRT017 Cartilage Disease 54 0.036
474
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.036
475
RLP001 Relapsing Polychondritis 54 0.036
476
PPL022 Papilloma 54 0.036
477
MYM001 Myoma 54 0.036
478
PNC001 Pancytopenia 54 0.036
479
c PRD040 Periodontitis, Chronic 53 0.036
480
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.036
481
P DDN001 Duodenal Ulcer 52 0.036
482
c THY107 Thymoma, Familial 52 0.036
484
P OBS001 Obstructive Jaundice 50 0.036
485
HMG002 Hemoglobinuria 50 0.036
486
OPT003 Opiate Dependence 50 0.036
487
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.036
488
FCL012 Facial Paralysis 46 0.036
489
KRT013 Keratolytic Winter Erythema 46 0.036
490
OPD001 Opioid Abuse 46 0.036
491
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.036
492
ASP008 Aspiration Pneumonitis 45 0.036
493
c PRM038 Primary Agammaglobulinemia 44 0.036
494
TRP009 Triple X Syndrome 42 0.036
495
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.036
496
PHM001 Phimosis 37 0.036
497
c PRS136 Prostate Cancer, Hereditary, 6 33 0.036
498
c PRS130 Prostate Cancer, Hereditary, 8 32 0.036
499
ACN019 Acanthamoeba Keratitis 31 0.036
500
P LNG032 Lung Cancer 98 0.034
501
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.034
502
P HNT016 Huntington Disease 72 0.034
503
c LKM063 Leukemia, Chronic Myeloid 72 0.034
504
ACR007 Acromegaly 71 0.034
505
P SRC025 Sarcoidosis 1 70 0.034
506
P ANG001 Angelman Syndrome 69 0.034
507
ALL003 Allergic Rhinitis 67 0.034
508
P HYP098 Hypereosinophilic Syndrome 67 0.034
509
P MTR014 Motor Neuron Disease 65 0.034
510
ATH013 Atherosclerosis Susceptibility 65 0.034
511
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.034
512
OST017 Osteomyelitis 64 0.034
513
P HML002 Hemolytic Anemia 63 0.034
514
P DST002 Distal Arthrogryposis 63 0.034
515
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.034
516
P VSC011 Vasculitis 62 0.034
517
MDD011 Mood Disorder 62 0.034
518
NTR005 Nutritional Deficiency Disease 62 0.034
519
P KDN017 Kidney Cancer 60 0.034
520
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.034
521
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.034
522
P GLY013 Glycogen Storage Disease 60 0.034
523
P BCL017 B-Cell Lymphoma 58 0.034
524
EYD002 Eye Disease 58 0.034
525
P RHN004 Rhinitis 57 0.034
526
TNS005 Tonsillitis 57 0.034
527
NRL004 Neuroleptic Malignant Syndrome 56 0.034
528
LMB062 Limb Ischemia 55 0.034
529
P DRR001 Diarrhea 55 0.034
530
c MYP132 Myopathy, Congenital 55 0.034
531
SYN007 Synovitis 54 0.034
532
P PMP001 Pemphigus 54 0.034
533
P INF037 Inflammatory Bowel Disease 54 0.034
534
PRC013 Pericarditis 54 0.034
535
GST023 Gastric Ulcer 53 0.034
536
P RTN018 Retinal Disease 53 0.034
537
MCN017 Meconium Ileus 52 0.034
538
P NRC002 Narcolepsy 52 0.034
539
MYL020 Myelomeningocele 51 0.034
540
CLB002 Clubfoot 51 0.034
541
PLC008 Placenta Disease 50 0.034
542
LFT001 Left Bundle Branch Hemiblock 49 0.034
543
OPD006 Opioid Addiction 48 0.034
544
SRT004 Serotonin Syndrome 47 0.034
545
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.034
546
SPN020 Spondylosis 46 0.034
547
STS002 Situs Inversus 45 0.034
548
MGS001 Megaesophagus 43 0.034
549
RST023 Resting Heart Rate, Variation in 41 0.034
550
RDN001 Reading Disorder 40 0.034
551
ANG049 Angioedema Induced by Ace Inhibitors 40 0.034
552
HRW001 Hair Whorl 36 0.034
553
PLC002 Plica Syndrome 36 0.034
554
BRK012 Broken Heart Syndrome 35 0.034
555
SHL001 Shoulder Impingement Syndrome 32 0.034
556
PST092 Posttransplant Acute Limbic Encephalitis 29 0.034
557
MYL069 Myeloma, Multiple 85 0.031
558
BRN028 Brain Cancer 74 0.031
559
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.031
560
P ATS364 Autism 70 0.031
561
APR006 Apert Syndrome 70 0.031
562
PLM001 Pulmonary Tuberculosis 69 0.031
563
LYM133 Lymphoma, Hodgkin, Classic 69 0.031
564
P LKM062 Leukemia, Acute Lymphoblastic 69 0.031
565
CHL065 Cholangiocarcinoma 68 0.031
566
P LKM002 Leukemia 68 0.031
567
SKN019 Skin Melanoma 68 0.031
568
P ESS003 Essential Thrombocythemia 68 0.031
569
P MJR001 Major Depressive Disorder 68 0.031
570
FCT007 Factor Vii Deficiency 67 0.031
571
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.031
572
c RHB024 Rhabdomyosarcoma 2 67 0.031
573
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.031
574
OST159 Osteogenic Sarcoma 66 0.031
575
c MCR129 Microvascular Complications of Diabetes 1 66 0.031
576
ACH004 Achondroplasia 66 0.031
577
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 0.031
578
c MCL013 Mucolipidosis Iv 66 0.031
579
c FML001 Familial Atrial Fibrillation 65 0.031
580
MSC007 Muscle Hypertrophy 64 0.031
581
c DPH024 Diaphragmatic Hernia, Congenital 63 0.031
582
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.031
583
CHN016 Cohen Syndrome 63 0.031
584
P END044 Endometriosis 63 0.031
585
c HPT001 Hepatitis C 62 0.031
586
P HYP750 Hypertriglyceridemia, Familial 62 0.031
587
P ORT004 Orthostatic Intolerance 62 0.031
588
INT002 Intermittent Claudication 61 0.031
589
GST033 Gestational Diabetes 61 0.031
590
DCB001 Decubitus Ulcer 61 0.031
591
PTN001 Patent Foramen Ovale 60 0.031
592
HPT019 Hepatic Encephalopathy 60 0.031
593
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.031
594
CHC001 Chickenpox 60 0.031
595
HYD002 Hydronephrosis 60 0.031
596
c OTP006 Otopalatodigital Syndrome, Type I 60 0.031
597
P MYC008 Myocarditis 59 0.031
598
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.031
599
PPT005 Peptic Ulcer Disease 59 0.031
600
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.031
601
P ALC033 Alcohol Use Disorder 58 0.031
602
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.031
603
P PLV020 Pelvic Organ Prolapse 57 0.031
604
c VSC019 Vesicoureteral Reflux 1 57 0.031
605
P CRD246 Cardiovascular System Disease 57 0.031
606
c GRV008 Graves Disease 1 56 0.031
607
NRG002 Neurogenic Bladder 55 0.031
608
P ANT006 Antiphospholipid Syndrome 55 0.031
609
PRP009 Peripartum Cardiomyopathy 55 0.031
610
DXT001 Dextrocardia 55 0.031
611
URN010 Urinary Tract Obstruction 55 0.031
612
END040 Endogenous Depression 55 0.031
613
GLC003 Glucose Intolerance 54 0.031
614
TND005 Tendinitis 54 0.031
615
TRC062 Tricuspid Atresia 54 0.031
616
LYM040 Lymphoblastic Lymphoma 54 0.031
617
SNS003 Sensory Peripheral Neuropathy 54 0.031
618
OCL006 Ocular Hypertension 53 0.031
619
GTR002 Goiter 53 0.031
620
c CNT035 Central Nervous System Disease 52 0.031
621
EXP004 Exophthalmos 52 0.031
622
c VRL010 Viral Hepatitis 52 0.031
623
CRT016 Carotid Artery Disease 52 0.031
624
P PRR016 Pierre Robin Syndrome 52 0.031
625
SPS003 Spastic Diplegia 51 0.031
626
INT079 Intrahepatic Cholangiocarcinoma 51 0.031
627
NRM004 Neuroma 51 0.031
628
TNG007 Tongue Carcinoma 51 0.031
629
PLR007 Pleural Empyema 50 0.031
630
LNT004 Lentigines 50 0.031
631
P OVR082 Overgrowth Syndrome 50 0.031
632
RSP006 Respiratory System Disease 50 0.031
633
HYP748 Hypertelorism 50 0.031
634
ENT004 Enthesopathy 49 0.031
635
CCN002 Cocaine Abuse 49 0.031
636
RYN001 Raynaud Disease 48 0.031
637
BRS064 Bursitis 48 0.031
638
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.031
639
CYS002 Cystic Lymphangioma 48 0.031
640
PYL006 Pyloric Stenosis 48 0.031
641
PRP007 Priapism 47 0.031
642
LRY029 Laryngomalacia 47 0.031
643
P CRN028 Corneal Ulcer 47 0.031
644
c INH020 Inherited Metabolic Disorder 47 0.031
645
c CNG216 Congenital Hydrocephalus 47 0.031
646
P OVR046 Ovarian Cyst 47 0.031
647
LYM019 Lymphosarcoma 46 0.031
648
CLN045 Colonic Benign Neoplasm 46 0.031
649
HPT004 Hepatic Coma 45 0.031
650
URL001 Urolithiasis 45 0.031
651
P PRD021 Periodic Paralysis 45 0.031
652
MYF001 Myofibroma 45 0.031
653
PRM003 Premature Ejaculation 44 0.031
654
P MYG005 Myoglobinuria 44 0.031
655
DVR002 Diverticulitis 43 0.031
656
P CRN026 Corneal Edema 43 0.031
657
PLY068 Polysubstance Abuse 43 0.031
658
P MJR007 Major Affective Disorder 1 43 0.031
659
TRC097 Tracheomalacia 42 0.031
660
P CHR342 Chiari Malformation 41 0.031
661
LTX001 Latex Allergy 41 0.031
662
ART008 Arteriosclerosis Obliterans 40 0.031
663
MLG086 Malignant Hyperthermia Susceptibility 39 0.031
664
P DYS021 Dysautonomia 39 0.031
665
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.031
666
OVR094 Ovarian Epithelial Cancer 38 0.031
667
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.031
668
CHL013 Cholecystolithiasis 37 0.031
669
EPD005 Epidural Abscess 35 0.031
670
WBR001 Weber Syndrome 35 0.031
671
c MJR008 Major Affective Disorder 2 35 0.031
672
c ACQ047 Acquired Methemoglobinemia 34 0.031
673
c MJR023 Major Affective Disorder 7 33 0.031
674
EMP011 Emphysema, Congenital Lobar 33 0.031
675
c MJR003 Major Affective Disorder 6 33 0.031
676
c MJR006 Major Affective Disorder 5 33 0.031
677
HLT002 Halothane Hepatitis 32 0.031
678
c MJR004 Major Affective Disorder 4 28 0.031
679
CRT028 Cor Triatriatum 26 0.031
680
c LKM061 Leukemia, Acute Myeloid 84 0.029
681
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.029
682
c NRF023 Neurofibromatosis, Type Ii 80 0.029
683
CNN003 Conn's Syndrome 79 0.029
684
P APL001 Aplastic Anemia 74 0.029
685
P OST002 Osteoporosis 74 0.029
686
c HYP836 Hypercholesterolemia, Familial, 1 73 0.029
687
ULC004 Ulcerative Colitis 73 0.029
688
MYL009 Myelodysplastic Syndrome 70 0.029
689
MLT157 Multiple System Atrophy 1 70 0.029
690
LGH007 Leigh Syndrome 70 0.029
691
P OCL013 Oculodentodigital Dysplasia 69 0.029
692
P BLD062 Bile Duct Cancer 67 0.029
693
c ATS007 Autism Spectrum Disorder 67 0.029
694
GLL008 Gilles De La Tourette Syndrome 66 0.029
695
P BRD002 Bardet-Biedl Syndrome 66 0.029
696
c SML038 Small Cell Cancer of the Lung 65 0.029
697
P CNJ013 Conjunctivitis 65 0.029
698
SRC014 Sarcoma 65 0.029
699
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.029
700
c JVN010 Juvenile Rheumatoid Arthritis 64 0.029
701
GT001 Gout 64 0.029
702
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.029
703
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.029
704
TRN015 Transient Cerebral Ischemia 63 0.029
705
ANR007 Anorexia Nervosa 63 0.029
706
CLT003 Colitis 62 0.029
707
P PSR002 Psoriasis 62 0.029
708
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.029
709
P DRM010 Dermatomyositis 61 0.029
710
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.029
711
P MYL006 Myeloid Leukemia 60 0.029
712
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.029
713
FCT002 Factor Xi Deficiency 60 0.029
714
c HRD002 Hereditary Angioedema 60 0.029
715
c HPT016 Hepatitis B 59 0.029
716
P GLL022 Guillain-Barre Syndrome 59 0.029
717
PMP006 Pemphigus Vulgaris, Familial 57 0.029
718
BRN056 Bronchopulmonary Dysplasia 57 0.029
719
P URF003 Urofacial Syndrome 1 57 0.029
720
HMR039 Hemorrhage, Intracerebral 57 0.029
721
P MYS005 Myositis 56 0.029
722
c ESS001 Essential Tremor 56 0.029
723
BCT022 Bacterial Infectious Disease 56 0.029
724
GNR004 Generalized Anxiety Disorder 56 0.029
725
ALL010 Allergic Contact Dermatitis 56 0.029
726
GST050 Gastrointestinal System Disease 56 0.029
727
P SCK004 Seckel Syndrome 56 0.029
728
P AGN002 Agnosia 55 0.029
729
P ATR001 Atrioventricular Septal Defect 55 0.029
730
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.029
731
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.029
732
P SPN052 Spondyloarthropathy 54 0.029
733
PTT009 Pituitary Gland Disease 54 0.029
734
P END047 Endophthalmitis 53 0.029
735
MTN003 Motion Sickness 53 0.029
736
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.029
737
HMC014 Homocysteinemia 53 0.029
738
SPN035 Spindle Cell Sarcoma 53 0.029
739
NRT001 Neurotic Disorder 53 0.029
740
PST011 Pustulosis of Palm and Sole 52 0.029
741
AVD001 Avoidant Personality Disorder 51 0.029
742
LNG031 Lung Benign Neoplasm 51 0.029
743
ESP002 Esophageal Varix 51 0.029
744
SPN019 Spondylolisthesis 51 0.029
745
P CHL066 Cholangitis 51 0.029
746
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.029
747
SCH012 Schizoaffective Disorder 50 0.029
748
PST021 Postpartum Depression 50 0.029
749
ECT026 Ectopic Pregnancy 50 0.029
750
P OMP004 Omphalocele 50 0.029
751
BTY001 Butyrylcholinesterase Deficiency 50 0.029
752
BKR002 Baker-Gordon Syndrome 49 0.029
753
P MGR001 Migraine Without Aura 49 0.029
754
HST010 Histiocytosis 48 0.029
755
CCN001 Cocaine Dependence 48 0.029
756
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.029
757
HMP001 Hemopericardium 48 0.029
758
URN009 Urinary System Disease 48 0.029
759
DRG003 Drug Dependence 47 0.029
760
c MCR120 Microvascular Complications of Diabetes 7 47 0.029
761
P ENC008 Encephalocele 47 0.029
762
c PRM093 Premature Ovarian Failure 7 47 0.029
763
ANL022 Anal Fistula 46 0.029
764
SMT001 Somatization Disorder 46 0.029
765
RTR001 Retrograde Amnesia 44 0.029
766
c CHR579 Chiari Malformation Type Ii 44 0.029
767
SPN369 Spinal Disease 43 0.029
768
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.029
769
ORB013 Orbital Disease 42 0.029
770
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.029
771
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.029
772
EPC002 Epicondylitis 41 0.029
773
49X006 49, Xxxxy Syndrome 41 0.029
774
DBT002 Diabetic Autonomic Neuropathy 41 0.029
775
P SCL057 Scoliosis, Isolated 1 41 0.029
776
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.029
777
c PLM022 Pulmonary Valve Insufficiency 39 0.029
778
FML039 Female Reproductive System Disease 39 0.029
779
c CHR682 Chronic Bilirubin Encephalopathy 39 0.029
780
ANT019 Anterograde Amnesia 38 0.029
781
HYP264 Hypertonia 38 0.029
782
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.029
783
BLR028 Biliary Atresia, Extrahepatic 37 0.029
784
ABD010 Abdominal Wall Defect 36 0.029
785
CRV025 Cervical Incompetence 34 0.029
786
HND015 Hand Skill, Relative 33 0.029
787
FNT004 Fainting 30 0.029
788
RSP007 Respiratory Distress Syndrome, Infant 30 0.029
789
ISL075 Isolated Pierre Robin Sequence 29 0.029
790
PRK076 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 28 0.029
791
ATR089 Atrioventricular Dissociation 20 0.029
792
c QTN001 Qt Interval, Variation in 13 0.029
793
P LKM071 Leukemia, Chronic Lymphocytic 79 0.027
794
ADR007 Adrenoleukodystrophy 75 0.027
795
c HPT073 Hepatitis C Virus 72 0.027
796
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.027
797
SMT004 Smith-Lemli-Opitz Syndrome 70 0.027
798
P TBR001 Tuberous Sclerosis 70 0.027
799
ACR008 Acrocallosal Syndrome 69 0.027
800
LYM007 Lymphangioleiomyomatosis 69 0.027
801
MNT001 Mantle Cell Lymphoma 69 0.027
802
P MYC084 Mycobacterium Tuberculosis 1 68 0.027
803
c BSL007 Basal Cell Carcinoma 68 0.027
804
OBS002 Obsessive-Compulsive Disorder 68 0.027
805
CST001 Costello Syndrome 68 0.027
806
CNN005 Connective Tissue Disease 68 0.027
807
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.027
808
c INF071 Inflammatory Bowel Disease 1 67 0.027
809
BRK010 Burkitt Lymphoma 67 0.027
810
P TRC072 Treacher Collins Syndrome 1 66 0.027
811
P SKN015 Skin Carcinoma 66 0.027
812
P MCR115 Microvascular Complications of Diabetes 5 66 0.027
813
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.027
814
P DRM053 Dermatitis, Atopic 66 0.027
815
MYL031 Myeloproliferative Neoplasm 66 0.027
816
P VNW001 Von Willebrand's Disease 65 0.027
817
OVR029 Ovarian Hyperstimulation Syndrome 64 0.027
818
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.027
819
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.027
820
PLM031 Poliomyelitis 64 0.027
821
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.027
822
KRN002 Kearns-Sayre Syndrome 63 0.027
823
P ANR048 Aniridia 1 63 0.027
824
PLG002 Plague 63 0.027
825
P THR117 Three M Syndrome 1 63 0.027
826
END041 Endometrial Adenocarcinoma 63 0.027
827
BDD001 Budd-Chiari Syndrome 63 0.027
828
P ECT006 Ectodermal Dysplasia 62 0.027
829
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.027
830
HMT002 Hematologic Cancer 62 0.027
831
c HPT003 Hepatitis a 62 0.027
832
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.027
833
c MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.027
834
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.027
835
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.027
836
CHR066 Chronic Fatigue Syndrome 61 0.027
837
NRL005 Neurilemmoma 60 0.027
838
c LPM012 Lipomatosis, Multiple 60 0.027
839
INT066 Interstitial Lung Disease 60 0.027
840
SQM006 Squamous Cell Carcinoma 60 0.027
841
ETN001 Eating Disorder 60 0.027
842
P THL005 Thalassemia 60 0.027
843
PRN019 Perinatal Necrotizing Enterocolitis 59 0.027
844
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.027
845
P BRS044 Breast Adenocarcinoma 59 0.027
846
P PLY006 Polydactyly 59 0.027
847
BRS051 Breast Disease 58 0.027
848
LYM027 Lymphopenia 58 0.027
849
P GLL018 Gallbladder Cancer 57 0.027
850
P ESP035 Esophagitis, Eosinophilic, 1 57 0.027
851
GLS018 Glass Syndrome 57 0.027
852
P PLY041 Polymyositis 57 0.027
853
THY122 Thyroid Gland Cancer 57 0.027
854
BRD001 Brody Myopathy 57 0.027
855
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.027
856
BLR008 Bilirubin Metabolic Disorder 57 0.027
857
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.027
858
CMR002 Coumarin Resistance 56 0.027
859
LMY014 Leiomyoma, Uterine 56 0.027
860
SCH003 Schizophreniform Disorder 56 0.027
861
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.027
862
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.027
863
MCL006 Macular Retinal Edema 55 0.027
864
ZLL002 Zollinger-Ellison Syndrome 55 0.027
865
P GRV001 Graves' Disease 55 0.027
866
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.027
867
ESN005 Eosinophilic Gastroenteritis 55 0.027
868
GST037 Gastroparesis 54 0.027
869
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.027
870
NNL006 Non-Alcoholic Steatohepatitis 54 0.027
871
P TCD001 Tic Disorder 53 0.027
872
RHM028 Rheumatic Heart Disease 53 0.027
873
CRH005 Crohn's Colitis 53 0.027
874
BRN038 Bronchial Disease 53 0.027
875
P PLM006 Pulmonary Alveolar Proteinosis 53 0.027
876
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.027
877
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.027
878
P PNC025 Panic Disorder 53 0.027
879
c FML191 Familial Long Qt Syndrome 53 0.027
880
THY030 Thyroid Gland Disease 52 0.027
881
BWN001 Bowen-Conradi Syndrome 52 0.027
882
FML037 Female Breast Cancer 52 0.027
883
P MGR003 Migraine with Aura 52 0.027
884
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.027
885
PLS009 Plasma Cell Neoplasm 51 0.027
886
ENT011 Enterocolitis 51 0.027
887
c PNC106 Pancreatic Agenesis 1 51 0.027
888
P PRC012 Pericardial Effusion 51 0.027
889
SKN013 Skin Benign Neoplasm 51 0.027
890
ACT017 Acute Chest Syndrome 51 0.027
891
RTN003 Retinal Ischemia 50 0.027
892
P BRT029 Brittle Cornea Syndrome 2 50 0.027
893
STM007 Stomatitis 50 0.027
894
ALN001 Aland Island Eye Disease 50 0.027
895
P TMP001 Temporal Lobe Epilepsy 50 0.027
896
NTR046 Neutrophil Migration 50 0.027
897
P OTS001 Otosclerosis 49 0.027
898
ART017 Aortic Disease 49 0.027
899
P MST002 Mast-Cell Leukemia 49 0.027
900
SNT005 Sinoatrial Node Disease 49 0.027
901
P OPN001 Open-Angle Glaucoma 49 0.027
902
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.027
903
ADR016 Adrenal Cortical Carcinoma 48 0.027
904
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.027
905
PNC034 Pancreas Disease 48 0.027
906
DGN001 Degenerative Disc Disease 48 0.027
907
P TRT019 Torticollis 48 0.027
908
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.027
909
DRY001 Dry Eye Syndrome 47 0.027
910
THY128 Thyroid Tumor 47 0.027
911
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.027
912
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.027
913
ASP004 Asphyxia Neonatorum 46 0.027
914
MGC001 Megacolon 46 0.027
915
SQM002 Squamous Cell Papilloma 46 0.027
916
c DRR009 Diarrhea 6 46 0.027
917
c MLG068 Malignant Glioma 46 0.027
918
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.027
919
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.027
920
PRL008 Paralytic Ileus 45 0.027
921
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.027
922
CNT017 Central Nervous System Origin Vertigo 45 0.027
923
ANS012 Anus Disease 45 0.027
924
c DRM054 Dermatitis, Atopic, 2 44 0.027
925
CNN002 Cannabis Abuse 44 0.027
926
PPL001 Papillary Adenoma 44 0.027
927
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.027
928
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.027
929
DPR002 Depersonalization Disorder 43 0.027
930
TND004 Tendinopathy 43 0.027
931
URT037 Urethral Stricture 43 0.027
932
c SRC023 Sarcoidosis 2 43 0.027
933
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.027
934
OCL052 Ocular Dominance 42 0.027
935
PCD001 Pica Disease 41 0.027
936
PLM005 Pleomorphic Lipoma 40 0.027
937
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.027
938
HYP540 Hypertension, Diastolic 40 0.027
939
CNN001 Cannabis Dependence 40 0.027
940
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.027
941
SPR024 Supratentorial Cancer 39 0.027
942
ADN067 Adenoid Hypertrophy 39 0.027
943
ALX002 Alexithymia 38 0.027
944
CHL039 Choledocholithiasis 38 0.027
945
c OVR114 Ovarian Cancer 1 38 0.027
946
ALG027 Al-Gazali-Bakalinova Syndrome 38 0.027
947
c SYS043 Systemic Lupus Erythematosus 1 38 0.027
948
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.027
949
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.027
950
ENP001 Enophthalmos 35 0.027
951
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.027
952
P ENT005 Entropion 34 0.027
953
PLM028 Pulmonary Coin Lesion 33 0.027
954
CRB031 Cerebral Arterial Disease 33 0.027
955
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.027
956
PRS064 Persistent Vegetative State 33 0.027
957
SBV001 Subvalvular Aortic Stenosis 33 0.027
958
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.027
959
LGP001 Lagophthalmos 30 0.027
960
PRP013 Paraphimosis 30 0.027
961
c OTS005 Otosclerosis 1 29 0.027
962
P PPL023 Pupil Disease 28 0.027
963
HMC012 Hemicrania Continua 28 0.027
964
CYT018 Cytochrome P450 2d6 Variant 27 0.027
965
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.027
966
DVR001 Diverticulitis of Colon 25 0.027
967
INT053 Intracranial Vasospasm 24 0.027
968
P GLM040 Glioma Susceptibility 1 81 0.024
969
GST019 Gastrointestinal Stromal Tumor 78 0.024
970
P NNN008 Noonan Syndrome 1 76 0.024
971
GLB015 Glioblastoma Multiforme 75 0.024
972
c ART115 Aortic Valve Disease 1 75 0.024
973
c HMC039 Hemochromatosis, Type 1 74 0.024
974
c BTT014 Beta-Thalassemia 74 0.024
975
SVR004 Severe Combined Immunodeficiency 73 0.024
976
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.024
977
P RTN024 Retinoblastoma 73 0.024
978
P JBR020 Joubert Syndrome 1 72 0.024
979
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.024
980
MYL005 Myelofibrosis 70 0.024
981
MCC012 Mccune-Albright Syndrome 70 0.024
982
c PNC108 Pancreatitis, Hereditary 70 0.024
983
P ASP006 Aspergillosis 69 0.024
984
SVR097 Severe Cutaneous Adverse Reaction 69 0.024
985
c MYT021 Myotonic Dystrophy 1 69 0.024
986
P INF038 Influenza 68 0.024
987
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.024
988
PNC129 Pancreatic Adenocarcinoma 68 0.024
989
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.024
990
P FLL037 Follicular Lymphoma 67 0.024
991
FLL027 Fallopian Tube Carcinoma 67 0.024
992
MYC006 Mycosis Fungoides 66 0.024
993
P NSP012 Nasopharyngeal Carcinoma 66 0.024
994
P MNN013 Meningitis 66 0.024
995
CRN036 Craniopharyngioma 65 0.024
996
BRR014 Barrett Esophagus 65 0.024
997
IRR002 Irritable Bowel Syndrome 65 0.024
998
P PRS038 Personality Disorder 65 0.024
999
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.024
1000
ART002 Arts Syndrome 64 0.024
1001
DGR001 Digeorge Syndrome 64 0.024
1002
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.024
1003
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.024
1004
P GCH001 Gaucher's Disease 63 0.024
1005
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.024
1006
MSC152 Muscular Dystrophy, Becker Type 63 0.024
1007
INT146 Intervertebral Disc Disease 63 0.024
1008
c SYS004 Systemic Mastocytosis 63 0.024
1009
P LMY004 Leiomyosarcoma 63 0.024
1010
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.024
1011
BRS099 Breast Ductal Carcinoma 62 0.024
1012
PSR001 Psoriatic Arthritis 61 0.024
1013
WLD007 Waldenstroem's Macroglobulinemia 61 0.024
1014
ART141 Arteriovenous Malformations of the Brain 61 0.024
1015
P SJG008 Sjogren Syndrome 61 0.024
1016
WLL001 Williams-Beuren Syndrome 60 0.024
1017
SZR001 Sezary's Disease 60 0.024
1018
CNT105 Central Core Disease of Muscle 60 0.024
1019
c JVN061 Juvenile Arthritis 60 0.024
1020
P CHR285 Chronic Myelomonocytic Leukemia 60 0.024
1021
CHL014 Cholera 59 0.024
1022
P LYM033 Lymphoproliferative Syndrome 59 0.024
1023
DCT002 Ductal Carcinoma in Situ 59 0.024
1024
GRD007 Grade Iii Astrocytoma 59 0.024
1025
GNG013 Gingivitis 59 0.024
1026
BRN002 Bronchiolitis 59 0.024
1027
P ANP001 Anaplastic Large Cell Lymphoma 58 0.024
1028
c PRM005 Primary Hyperparathyroidism 58 0.024
1029
ERY003 Erythema Multiforme 58 0.024
1030
P BNC003 Bone Cancer 58 0.024
1031
P CND004 Candidiasis 58 0.024
1032
P GLM007 Glomerulonephritis 57 0.024
1033
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.024
1034
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.024
1035
c MST023 Mesothelioma, Malignant 57 0.024
1036
STR081 Stormorken Syndrome 57 0.024
1037
LNN001 Lennox-Gastaut Syndrome 57 0.024
1038
INT303 Intracranial Hypertension, Idiopathic 57 0.024
1039
c BSL024 Basal Cell Carcinoma 1 56 0.024
1040
P ADL017 Adult T-Cell Leukemia 56 0.024
1041
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.024
1042
P CHN012 Chondrosarcoma 56 0.024
1043
P PLY011 Polycystic Ovary Syndrome 56 0.024
1044
HMT008 Hematuria, Benign Familial 56 0.024
1045
PLS011 Plasmacytoma 56 0.024
1046
SFT003 Soft Tissue Sarcoma 56 0.024
1047
DBL002 Double Outlet Right Ventricle 56 0.024
1048
MTH009 Mouth Disease 56 0.024
1049
HMG005 Hemoglobinopathy 56 0.024
1050
PRN038 Prune Belly Syndrome 56 0.024
1051
P RST002 Restrictive Cardiomyopathy 56 0.024
1052
BRN012 Bronchiolitis Obliterans 55 0.024
1053
MCN007 Meconium Aspiration Syndrome 55 0.024
1054
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.024
1055
ADR008 Adrenal Adenoma 55 0.024
1056
P DYS193 Dystonia 11, Myoclonic 55 0.024
1057
HRY003 Hairy Cell Leukemia 55 0.024
1058
GLS001 Gliosarcoma 54 0.024
1059
P ALP008 Alopecia 54 0.024
1060
FCL014 Focal Epilepsy 54 0.024
1061
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.024
1062
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.024
1063
THR013 Thoracic Outlet Syndrome 54 0.024
1064
GST009 Gastroschisis 53 0.024
1065
P LCH002 Lichen Planus 53 0.024
1066
MMM001 Mammary Paget's Disease 53 0.024
1067
PST046 Post-Transplant Lymphoproliferative Disease 53 0.024
1068
P RTN016 Retinal Degeneration 53 0.024
1069
BRD004 Borderline Personality Disorder 53 0.024
1070
P CNT005 Central Nervous System Lymphoma 53 0.024
1071
P HMR003 Hemorrhagic Disease 53 0.024
1072
P FBR031 Febrile Seizures 53 0.024
1073
P RTN022 Retinal Vein Occlusion 53 0.024
1074
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.024
1075
PRP080 Peripheral Artery Disease 53 0.024
1076
c FML008 Familial Retinoblastoma 53 0.024
1077
P INT068 Intestinal Disease 53 0.024
1078