Search results for Cocaine

1221 hits were found for Cocaine

# Family MCID Name MIFTS Score
1
CCN002 Cocaine Abuse 49 7.757
2
CCN001 Cocaine Dependence 48 7.481
3
CCN012 Cocaine Antenatal Exposure 14 5.389
4
CCN009 Cocaine Intoxication 27 4.734
5
CCN010 Cocaine Embryofetopathy 13 4.183
6
P SBS003 Substance Abuse 55 0.494
7
ALC007 Alcohol Dependence 66 0.292
8
DRG003 Drug Dependence 47 0.290
9
P VSC011 Vasculitis 62 0.279
10
P SZR006 Seizure Disorder 56 0.250
11
VSL002 Visual Epilepsy 59 0.247
12
OPT003 Opiate Dependence 50 0.237
13
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.236
14
P PRS038 Personality Disorder 65 0.235
15
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.216
16
P ALC033 Alcohol Use Disorder 58 0.215
17
ISC004 Ischemia 58 0.214
18
P MYC007 Myocardial Infarction 70 0.209
19
SBS004 Substance Dependence 48 0.200
20
ANX010 Anxiety 73 0.193
21
DPR016 Depression 63 0.170
22
ART074 Aortic Dissection 52 0.170
23
ANT011 Antisocial Personality Disorder 47 0.165
24
P NTR004 Neutropenia 63 0.159
25
c ACT071 Acute Kidney Failure 60 0.157
26
GRN017 Granulocytopenia 44 0.157
27
PSY004 Psychotic Disorder 67 0.156
28
MNT002 Mental Depression 58 0.156
29
c ACT075 Acute Myocardial Infarction 57 0.155
30
PLC007 Placental Abruption 48 0.153
31
AVD001 Avoidant Personality Disorder 51 0.152
32
PLY068 Polysubstance Abuse 43 0.152
33
P SYP003 Syphilis 58 0.148
34
PRP030 Purpura 54 0.148
35
OPD006 Opioid Addiction 48 0.142
36
P MYC008 Myocarditis 59 0.139
37
P KDN018 Kidney Disease 72 0.137
38
TBC004 Tobacco Addiction 64 0.137
39
CRD132 Cardiac Conduction Defect 58 0.137
40
SBC016 Subacute Delirium 44 0.136
41
SVR004 Severe Combined Immunodeficiency 73 0.134
42
P CRD119 Cardiac Arrest 67 0.134
43
OPD001 Opioid Abuse 46 0.134
44
MDD011 Mood Disorder 62 0.131
45
WTH001 Withdrawal Disorder 48 0.131
46
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.129
47
P BPL003 Bipolar Disorder 56 0.127
48
PLM010 Pulmonary Edema 54 0.126
49
c MJR024 Major Affective Disorder 9 41 0.126
50
c MJR022 Major Affective Disorder 8 38 0.126
51
STR067 Stroke, Ischemic 81 0.124
52
P MJR001 Major Depressive Disorder 68 0.124
53
P EXN002 Exanthem 57 0.122
54
48X005 48,xyyy 39 0.122
55
THR024 Thrombosis 57 0.121
56
CRN019 Coronary Artery Vasospasm 46 0.121
57
HRN003 Heroin Dependence 44 0.121
58
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.115
59
SDD001 Sudden Infant Death Syndrome 61 0.113
60
PST028 Post-Traumatic Stress Disorder 58 0.111
61
PNM008 Pneumothorax 56 0.111
62
P SCH015 Schizophrenia 74 0.109
63
ACQ007 Acquired Immunodeficiency Syndrome 60 0.109
64
ACT084 Acute Stress Disorder 47 0.109
65
CNN001 Cannabis Dependence 40 0.109
66
c ATR087 Atrial Standstill 1 75 0.107
67
P TRM003 Tremor 54 0.107
68
STT001 Status Epilepticus 60 0.105
69
c DLT002 Dilated Cardiomyopathy 79 0.103
70
IMM167 Immune Deficiency Disease 78 0.103
71
HMN044 Human Immunodeficiency Virus Type 1 71 0.103
72
P VSC007 Vascular Disease 63 0.103
73
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.103
74
CHL014 Cholera 59 0.101
75
P GLM007 Glomerulonephritis 57 0.101
76
P HDC001 Headache 57 0.101
77
PNG002 Pain Agnosia 51 0.101
78
47X002 47,xyy 49 0.101
79
LPP008 Lipoprotein Quantitative Trait Locus 62 0.097
80
PTH002 Pathological Gambling 49 0.097
81
CRB039 Cerebrovascular Disease 67 0.092
82
ETN001 Eating Disorder 60 0.092
83
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.090
84
CNG034 Congestive Heart Failure 69 0.090
85
P PLM037 Pulmonary Hypertension 67 0.090
86
P END033 Endocarditis 57 0.090
87
CND002 Conduct Disorder 51 0.090
88
CRN017 Coronary Thrombosis 47 0.090
89
P THR014 Thrombocytopenia 67 0.088
90
P DYS154 Dystonia 65 0.088
91
ENT011 Enterocolitis 51 0.088
92
GRN037 Granulomatosis with Polyangiitis 65 0.085
93
CLT003 Colitis 62 0.085
94
c HPT001 Hepatitis C 62 0.085
95
P ENC018 Encephalopathy 61 0.085
96
P MCR010 Microcephaly 59 0.085
97
OCL069 Ocular Motor Apraxia 51 0.085
98
BRN071 Brain Injury 49 0.085
99
CNN002 Cannabis Abuse 44 0.085
100
ISC015 Ischemic Colitis 44 0.085
101
P HRT032 Heart Disease 75 0.083
102
PRN019 Perinatal Necrotizing Enterocolitis 59 0.083
103
ART140 Arteries, Anomalies of 52 0.083
104
CYT002 Cytokine Deficiency 42 0.083
105
c THR092 Thrombophilia Due to Thrombin Defect 73 0.080
106
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.080
107
HYP020 Hyperprolactinemia 64 0.080
108
DSS008 Disease of Mental Health 58 0.080
109
TRM010 Traumatic Brain Injury 51 0.080
110
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.077
111
P NRB001 Neuroblastoma 72 0.077
112
P PNC025 Panic Disorder 53 0.077
113
P NRC002 Narcolepsy 52 0.077
114
SYN036 Syncope 45 0.077
115
ATX019 Ataxia with Vitamin E Deficiency 42 0.077
116
THR123 Thrombotic Microangiopathy 36 0.077
117
P PRK057 Parkinson Disease, Late-Onset 78 0.075
118
PRT037 Pertussis 65 0.075
119
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.075
120
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.075
121
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.075
122
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.075
123
CRN030 Coronary Stenosis 50 0.075
124
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.075
125
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.075
126
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.075
127
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.075
128
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.075
129
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.075
130
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.075
131
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.075
132
P RSP003 Respiratory Failure 74 0.072
133
P BRG001 Brugada Syndrome 71 0.072
134
ANG054 Angina Pectoris 66 0.072
135
P ART005 Arteriovenous Malformation 65 0.072
136
c PRC016 Pre-Eclampsia 63 0.072
137
P MVM001 Movement Disease 63 0.072
138
ANR040 Aneurysm 59 0.072
139
BRD004 Borderline Personality Disorder 53 0.072
140
INT067 Interstitial Nephritis 48 0.072
141
P HRN001 Horner's Syndrome 45 0.072
142
c HPT073 Hepatitis C Virus 72 0.069
143
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.069
144
ALL026 Allergic Hypersensitivity Disease 62 0.069
145
P FTL001 Fetal Alcohol Syndrome 57 0.069
146
NRL004 Neuroleptic Malignant Syndrome 56 0.069
147
PYD001 Pyoderma Gangrenosum 54 0.069
148
END086 End Stage Renal Disease 51 0.069
149
PYD002 Pyoderma 50 0.069
150
MTB004 Metabolic Acidosis 50 0.069
151
HYP264 Hypertonia 38 0.069
152
P PHC003 Pheochromocytoma 71 0.065
153
c CHR684 Chronic Kidney Disease 70 0.065
154
P HPT021 Hepatitis 67 0.065
155
P TRN020 Turner Syndrome 67 0.065
156
c MGR028 Migraine with or Without Aura 1 67 0.065
157
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.065
158
ATM095 Autoimmune Disease 62 0.065
159
P OPT006 Optic Nerve Disease 60 0.065
160
DYS073 Dysphagia 50 0.065
161
SXL003 Sexual Disorder 47 0.065
162
PRP007 Priapism 47 0.065
163
c MLG069 Malignant Hypertension 47 0.065
164
CRD137 Cardiogenic Shock 47 0.065
165
ADR040 Adrenal Gland Pheochromocytoma 46 0.065
166
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.065
167
ANC002 Anca-Associated Vasculitis 41 0.065
168
P ALZ034 Alzheimer Disease 88 0.062
169
DWN001 Down Syndrome 70 0.062
170
HYP066 Hyperglycemia 61 0.062
171
P PNC044 Pancreatitis 61 0.062
172
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.062
173
P SLP005 Sleep Disorder 59 0.062
174
PLM033 Pulmonary Embolism 59 0.062
175
HYP266 Hypoxia 57 0.062
176
P NRP001 Neuropathy 56 0.062
177
P RTN014 Retinal Artery Occlusion 47 0.062
178
P HYP263 Hypersomnia 41 0.062
179
BRN026 Branch Retinal Artery Occlusion 40 0.062
180
c CNG033 Congenital Syphilis 40 0.062
182
c HYP595 Hypertension, Essential 84 0.058
183
LPT014 Leptin Deficiency or Dysfunction 74 0.058
184
ADL002 Adult Syndrome 70 0.058
185
OBS002 Obsessive-Compulsive Disorder 68 0.058
186
P HYP098 Hypereosinophilic Syndrome 67 0.058
187
HYP056 Hypoglycemia 66 0.058
188
LPD008 Lipid Metabolism Disorder 62 0.058
189
PNM010 Pneumothorax, Primary Spontaneous 60 0.058
190
c ACT027 Acute Pancreatitis 60 0.058
191
CRD223 Cardiac Arrhythmia 60 0.058
192
CHL123 Chlamydia 59 0.058
193
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.058
194
IRN002 Iron Metabolism Disease 57 0.058
195
P RHN004 Rhinitis 57 0.058
196
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.058
197
P HYP076 Hyperthyroidism 55 0.058
198
P TCD001 Tic Disorder 53 0.058
199
PLC008 Placenta Disease 50 0.058
200
DYS009 Dysthymic Disorder 49 0.058
201
c BPL002 Bipolar I Disorder 49 0.058
202
CRS001 Crescentic Glomerulonephritis 43 0.058
203
P MJR007 Major Affective Disorder 1 43 0.058
204
c CHR682 Chronic Bilirubin Encephalopathy 39 0.058
205
c MJR008 Major Affective Disorder 2 35 0.058
206
c MJR023 Major Affective Disorder 7 33 0.058
207
c MJR003 Major Affective Disorder 6 33 0.058
208
c MJR006 Major Affective Disorder 5 33 0.058
209
DFF031 Diffuse Alveolar Hemorrhage 30 0.058
210
c MJR004 Major Affective Disorder 4 28 0.058
211
PRP027 Peripheral Vascular Disease 71 0.055
212
P HYP086 Hypothyroidism 69 0.055
213
P PNM007 Pneumonia 68 0.055
214
KRT019 Keratitis, Hereditary 65 0.055
215
PRT036 Peritonitis 64 0.055
216
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.055
217
c FNC043 Fanconi Anemia, Complementation Group E 62 0.055
218
LNG099 Lung Disease 60 0.055
219
DSS009 Disseminated Intravascular Coagulation 57 0.055
220
c ACT134 Acute Liver Failure 56 0.055
221
P ANT006 Antiphospholipid Syndrome 55 0.055
222
END040 Endogenous Depression 55 0.055
223
AMN003 Amnestic Disorder 54 0.055
224
CLL003 Cellulitis 54 0.055
225
TXC002 Toxic Encephalopathy 53 0.055
226
SCH012 Schizoaffective Disorder 50 0.055
227
OPP004 Oppositional Defiant Disorder 49 0.055
228
ACT003 Acute Kidney Tubular Necrosis 45 0.055
229
P CHR345 Chronic Pain 44 0.055
230
c PRM038 Primary Agammaglobulinemia 44 0.055
231
c CNT028 Central Retinal Artery Occlusion 43 0.055
232
AMP007 Amphetamine Abuse 37 0.055
233
SPN185 Spinal Cord Infarction 28 0.055
234
MTR086 Motor Stereotypies 16 0.055
235
AST005 Asthma 76 0.051
236
c HYP836 Hypercholesterolemia, Familial, 1 73 0.051
237
P SYS005 Systemic Scleroderma 68 0.051
238
P LNG028 Long Qt Syndrome 66 0.051
239
ATH013 Atherosclerosis Susceptibility 65 0.051
240
P PRD008 Periodontitis 64 0.051
241
OST017 Osteomyelitis 64 0.051
242
ANR007 Anorexia Nervosa 63 0.051
243
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.051
244
P CTR002 Cataract 60 0.051
245
P INT070 Intestinal Obstruction 58 0.051
246
RBS001 Rabies 58 0.051
247
SCH003 Schizophreniform Disorder 56 0.051
248
AGN016 Aging 56 0.051
249
ATR057 Atrioventricular Block 55 0.051
250
LMB062 Limb Ischemia 55 0.051
251
P DRR001 Diarrhea 55 0.051
252
P STR020 Strabismus 55 0.051
253
HMP005 Hemiplegia 55 0.051
254
P ECL001 Eclampsia 50 0.051
255
RYN005 Raynaud Phenomenon 47 0.051
256
RTN020 Retinal Vascular Disease 46 0.051
257
HDN002 Head Injury 46 0.051
258
AGR002 Agoraphobia 45 0.051
259
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.051
260
P MYG005 Myoglobinuria 44 0.051
261
MCH006 Mechanical Strabismus 42 0.051
262
NNT008 Neonatal Abstinence Syndrome 41 0.051
263
CYC005 Cyclothymic Disorder 40 0.051
264
ALX002 Alexithymia 38 0.051
265
SBS005 Substance-Induced Psychosis 31 0.051
266
P EPL164 Epilepsy 71 0.046
267
c RHB024 Rhabdomyosarcoma 2 67 0.046
268
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.046
269
P DMN002 Dementia 66 0.046
270
P HYD006 Hydrocephalus 66 0.046
271
TTN003 Tetanus 65 0.046
272
TRN015 Transient Cerebral Ischemia 63 0.046
273
TXC005 Toxic Shock Syndrome 62 0.046
274
c HPT016 Hepatitis B 59 0.046
275
BRN002 Bronchiolitis 59 0.046
276
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.046
277
PMP006 Pemphigus Vulgaris, Familial 57 0.046
278
BLM002 Bulimia Nervosa 57 0.046
279
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.046
280
CMM005 Common Cold 57 0.046
281
GNR004 Generalized Anxiety Disorder 56 0.046
282
BRN012 Bronchiolitis Obliterans 55 0.046
283
HYP005 Hypokalemia 55 0.046
284
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.046
285
FDB001 Foodborne Botulism 55 0.046
286
INT007 Intermediate Coronary Syndrome 55 0.046
287
P PMP001 Pemphigus 54 0.046
288
P RST001 Restless Legs Syndrome 54 0.046
289
THR013 Thoracic Outlet Syndrome 54 0.046
290
P ART021 Arteriosclerosis 54 0.046
291
GSG001 Gas Gangrene 53 0.046
292
NRT001 Neurotic Disorder 53 0.046
293
INT051 Intussusception 53 0.046
294
c VRL010 Viral Hepatitis 52 0.046
295
PRV004 Periventricular Leukomalacia 52 0.046
296
P ESN008 Eosinophilic Pneumonia 50 0.046
297
LRN003 Learning Disability 49 0.046
298
QDR001 Quadriplegia 48 0.046
299
SCL003 Social Phobia 48 0.046
300
SRT004 Serotonin Syndrome 47 0.046
301
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.046
302
P CLS010 Cluster Headache 42 0.046
303
CRB086 Cerebral Aneurysms 40 0.046
304
PLC009 Placenta Praevia 39 0.046
305
c ATM104 Autoimmune Vasculitis 37 0.046
306
HRW001 Hair Whorl 36 0.046
308
CRT008 Carotid Artery Dissection 33 0.046
309
ANS021 Anisocoria 27 0.046
310
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.046
311
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.041
312
NRL016 Neural Tube Defects 82 0.041
313
CYS001 Cystic Fibrosis 81 0.041
314
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.041
315
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.041
316
P MLT020 Multiple Sclerosis 72 0.041
317
P HNT016 Huntington Disease 72 0.041
318
c EXD008 Exudative Vitreoretinopathy 1 71 0.041
319
DFC004 Deficiency Anemia 70 0.041
320
P MYP004 Myopathy 70 0.041
321
ACR008 Acrocallosal Syndrome 69 0.041
322
P SLP006 Sleep Apnea 69 0.041
323
P LVR013 Liver Disease 68 0.041
324
P MYS003 Myasthenia Gravis 68 0.041
325
P MLG056 Malignant Hyperthermia 67 0.041
326
P HRP006 Herpes Simplex 65 0.041
327
CLF027 Cleft Palate, Isolated 64 0.041
328
ART002 Arts Syndrome 64 0.041
329
MSC007 Muscle Hypertrophy 64 0.041
330
KRN002 Kearns-Sayre Syndrome 63 0.041
331
P HML002 Hemolytic Anemia 63 0.041
332
PLG002 Plague 63 0.041
333
MSS001 Masa Syndrome 62 0.041
334
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.041
335
VRL011 Viral Infectious Disease 61 0.041
336
DPH001 Diphtheria 60 0.041
337
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.041
338
P SNS001 Sensorineural Hearing Loss 60 0.041
339
ORL011 Oral Cancer 60 0.041
340
HYD002 Hydronephrosis 60 0.041
341
CNS004 Constipation 58 0.041
342
BRN056 Bronchopulmonary Dysplasia 57 0.041
343
APH002 Aphasia 57 0.041
344
GNT003 Genital Herpes 54 0.041
345
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.041
346
INF034 Infective Endocarditis 53 0.041
347
NRT004 Neuritis 52 0.041
348
CHR005 Chorioamnionitis 51 0.041
349
P MMB011 Membranous Nephropathy 50 0.041
350
PST021 Postpartum Depression 50 0.041
351
P SCK005 Sickle Cell Disease 50 0.041
352
PRN009 Paranoid Schizophrenia 50 0.041
353
VLV047 Volvulus of Midgut 49 0.041
354
P CMP008 Compartment Syndrome 49 0.041
355
ASP007 Aspiration Pneumonia 48 0.041
356
RGH001 Right Bundle Branch Block 48 0.041
357
DLS001 Delusional Disorder 47 0.041
358
P CRN028 Corneal Ulcer 47 0.041
359
SPC010 Speech and Communication Disorders 47 0.041
360
CHR074 Choriocarcinoma 47 0.041
361
P MYC033 Myoclonus 46 0.041
362
IMP006 Impulse Control Disorder 45 0.041
363
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.041
364
P HYP265 Hypotonia 43 0.041
365
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
366
PHB001 Phobic Disorder 41 0.041
367
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.041
368
SPL006 Splenic Infarction 38 0.041
369
CRB009 Cerebritis 37 0.041
370
P CRB088 Cerebral Atrophy 37 0.041
371
BRK012 Broken Heart Syndrome 35 0.041
372
CRN270 Coronary Artery Dissection, Spontaneous 32 0.041
373
P ACT028 Acute Closed-Angle Glaucoma 30 0.041
374
CYT018 Cytochrome P450 2d6 Variant 27 0.041
375
PHN001 Phencyclidine Abuse 24 0.041
376
P ATX030 Ataxia-Telangiectasia 82 0.036
377
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.036
378
P RTT002 Rett Syndrome 80 0.036
379
c SPN225 Spondyloarthropathy 1 73 0.036
380
P CNR004 Cone-Rod Dystrophy 2 73 0.036
381
P SRC025 Sarcoidosis 1 70 0.036
382
P FRG001 Fragile X Syndrome 70 0.036
383
P ASP006 Aspergillosis 69 0.036
384
ART016 Aortic Aneurysm 69 0.036
385
P ANG001 Angelman Syndrome 69 0.036
386
P MYC084 Mycobacterium Tuberculosis 1 68 0.036
387
RCK004 Rickets 68 0.036
388
CRP001 Carpal Tunnel Syndrome 67 0.036
389
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.036
390
ART001 Arterial Tortuosity Syndrome 66 0.036
391
AND002 Androgen Insensitivity Syndrome 66 0.036
392
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.036
393
BRR014 Barrett Esophagus 65 0.036
394
P ADL010 Adult Respiratory Distress Syndrome 65 0.036
395
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.036
396
P DBT009 Diabetes Mellitus 64 0.036
397
P ANR048 Aniridia 1 63 0.036
398
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.036
399
c MLG084 Malignant Fibrous Histiocytoma 63 0.036
400
SKN016 Skin Disease 63 0.036
401
P SHR029 Short Syndrome 63 0.036
402
c ACT068 Acute Cystitis 63 0.036
403
c SVR001 Severe Acute Respiratory Syndrome 62 0.036
404
P HYP750 Hypertriglyceridemia, Familial 62 0.036
405
P TRC086 Trichohepatoenteric Syndrome 1 62 0.036
406
OST003 Osteonecrosis 61 0.036
407
INT002 Intermittent Claudication 61 0.036
408
c PNS012 Paine Syndrome 61 0.036
409
c SCL052 Scleroderma, Familial Progressive 61 0.036
410
P ENC004 Encephalitis 61 0.036
411
SPN186 Spinal Cord Injury 60 0.036
412
ACN002 Acanthosis Nigricans 60 0.036
413
P AXN002 Axenfeld-Rieger Syndrome 59 0.036
414
PNM001 Pneumocystosis 59 0.036
415
P BRN022 Bronchiectasis 59 0.036
416
IRN001 Iron Deficiency Anemia 59 0.036
417
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.036
418
PPT005 Peptic Ulcer Disease 59 0.036
419
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.036
420
INT030 Intracranial Aneurysm 56 0.036
421
BRN004 Brain Edema 56 0.036
422
PRP009 Peripartum Cardiomyopathy 55 0.036
423
P ALP106 Alport Syndrome 1, X-Linked 55 0.036
424
BRN045 Brunner Syndrome 55 0.036
425
P FNG006 Feingold Syndrome 1 55 0.036
426
CLF004 Cleft Lip/palate 54 0.036
427
TRD006 Tardive Dyskinesia 54 0.036
428
PRT082 Preterm Premature Rupture of the Membranes 54 0.036
429
P LTR001 Lateral Sclerosis 54 0.036
430
GST009 Gastroschisis 53 0.036
431
CLF001 Cleft Lip 53 0.036
432
P PTS002 Ptosis 53 0.036
433
P FBR031 Febrile Seizures 53 0.036
434
GST023 Gastric Ulcer 53 0.036
435
c CNT035 Central Nervous System Disease 52 0.036
436
STT041 Stuttering 52 0.036
437
CHR073 Choreatic Disease 52 0.036
438
IMP005 Impotence 52 0.036
439
PTH003 Pathologic Nystagmus 52 0.036
440
TRC010 Trichotillomania 51 0.036
441
P LCT001 Lactic Acidosis 51 0.036
442
ACT049 Acute Disseminated Encephalomyelitis 51 0.036
443
P AST007 Astrocytoma 51 0.036
444
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.036
445
PLR007 Pleural Empyema 50 0.036
446
c SVR005 Severe Pre-Eclampsia 50 0.036
447
P MGR001 Migraine Without Aura 49 0.036
448
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.036
449
SPL018 Splenomegaly 48 0.036
450
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.036
451
P RNL015 Renal Hypertension 47 0.036
452
ATN005 Autonomic Dysfunction 46 0.036
453
P MTH007 Methemoglobinemia 46 0.036
454
c DRR009 Diarrhea 6 46 0.036
455
ANR004 Anuria 46 0.036
456
CRB004 Cerebral Artery Occlusion 45 0.036
457
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.036
458
HYD001 Hydranencephaly 44 0.036
459
GNG003 Gingival Recession 44 0.036
460
TRP009 Triple X Syndrome 42 0.036
461
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
462
MNN017 Mononeuropathy 42 0.036
463
GLC096 Galactorrhea 42 0.036
464
BCK006 Back Pain 42 0.036
465
ANX004 Anoxia 40 0.036
466
SCH011 Schizotypal Personality Disorder 40 0.036
467
P CRN074 Coronary Artery Aneurysm 39 0.036
468
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.036
469
BLC015 Balo Concentric Sclerosis 38 0.036
470
MLN003 Melancholia 38 0.036
471
FRN014 Fournier Gangrene 37 0.036
472
PLC006 Placental Choriocarcinoma 36 0.036
473
BRN018 Borna Disease 36 0.036
474
ABD010 Abdominal Wall Defect 36 0.036
475
ATX010 Ataxia Neuropathy Spectrum 34 0.036
476
ALR002 Al-Raqad Syndrome 33 0.036
477
ACT064 Acute Necrotizing Encephalitis 33 0.036
478
INF013 Inferior Myocardial Infarction 33 0.036
479
PHN011 Phenytoin Toxicity 33 0.036
480
HND015 Hand Skill, Relative 33 0.036
481
SSC001 Susac Syndrome 32 0.036
482
NRN002 Neuronitis 32 0.036
483
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.036
484
PLY150 Polykaryocytosis Inducer 31 0.036
485
ISL119 Isolated Optic Neuritis 30 0.036
486
PCM002 Pauci-Immune Glomerulonephritis 30 0.036
487
INT042 Internuclear Ophthalmoplegia 30 0.036
488
NCR003 Necrotizing Sialometaplasia 29 0.036
489
ARG004 Argyria 27 0.036
490
BLD137 Blood Group--Ahonen 16 0.036
492
P GST053 Gastric Cancer 83 0.029
493
PHN003 Phenylketonuria 75 0.029
494
GLB015 Glioblastoma Multiforme 75 0.029
495
SCK003 Sickle Cell Anemia 74 0.029
496
CRH001 Crohn's Disease 74 0.029
497
OTT002 Otitis Media 72 0.029
498
P AMY004 Amyloidosis 70 0.029
499
MLT157 Multiple System Atrophy 1 70 0.029
500
PLM001 Pulmonary Tuberculosis 69 0.029
501
CRB037 Cerebral Palsy 69 0.029
502
P INF038 Influenza 68 0.029
503
BRN024 Bronchitis 68 0.029
504
CNN005 Connective Tissue Disease 68 0.029
505
PNC129 Pancreatic Adenocarcinoma 68 0.029
506
WLF001 Wolff-Parkinson-White Syndrome 66 0.029
507
GLL008 Gilles De La Tourette Syndrome 66 0.029
508
P MCR115 Microvascular Complications of Diabetes 5 66 0.029
509
P MNN013 Meningitis 66 0.029
510
P PLM036 Pulmonary Fibrosis 65 0.029
511
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.029
512
ANG020 Angiosarcoma 64 0.029
513
P ADN016 Adenocarcinoma 64 0.029
514
SPT006 Septooptic Dysplasia 64 0.029
515
P GLM045 Glioma 63 0.029
516
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.029
517
P CRN300 Coronary Heart Disease 1 63 0.029
518
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.029
519
c HPT003 Hepatitis a 62 0.029
520
P ESP024 Esophagitis 62 0.029
521
P ORT004 Orthostatic Intolerance 62 0.029
522
P ACR001 Aicardi-Goutieres Syndrome 62 0.029
523
P OST009 Osteochondritis Dissecans 62 0.029
524
LVR012 Liver Cirrhosis 62 0.029
525
CHR001 Churg-Strauss Syndrome 61 0.029
526
ALC006 Alcoholic Hepatitis 61 0.029
527
CHR066 Chronic Fatigue Syndrome 61 0.029
528
APP008 Appendicitis 61 0.029
529
HRP004 Herpes Zoster 60 0.029
530
P NPH012 Nephrotic Syndrome 60 0.029
531
INT066 Interstitial Lung Disease 60 0.029
532
HPT019 Hepatic Encephalopathy 60 0.029
533
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.029
534
FBR047 Fibromyalgia 58 0.029
535
SPT004 Septic Arthritis 58 0.029
536
P EHL001 Ehlers-Danlos Syndrome 58 0.029
537
BRG013 Buerger Disease 58 0.029
538
P PRP019 Peripheral Nervous System Disease 58 0.029
539
P VND007 Van Der Woude Syndrome 1 58 0.029
540
P INF032 Infertility 57 0.029
541
GLS018 Glass Syndrome 57 0.029
542
P OPT009 Optic Neuritis 57 0.029
543
c ALZ056 Alzheimer Disease 3 57 0.029
544
P FCL005 Focal Segmental Glomerulosclerosis 57 0.029
545
P CRD246 Cardiovascular System Disease 57 0.029
546
PHR003 Pharyngitis 57 0.029
547
P ANG015 Angioedema 57 0.029
548
PRS047 Prostatitis 56 0.029
549
GST050 Gastrointestinal System Disease 56 0.029
550
MCR141 Mucormycosis 56 0.029
551
PRN038 Prune Belly Syndrome 56 0.029
552
NRN004 Neuroendocrine Tumor 55 0.029
553
ANG005 Anogenital Venereal Wart 55 0.029
554
P GRV001 Graves' Disease 55 0.029
555
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.029
556
CRT017 Cartilage Disease 54 0.029
557
P ALP008 Alopecia 54 0.029
558
FCL014 Focal Epilepsy 54 0.029
559
GST037 Gastroparesis 54 0.029
560
P END047 Endophthalmitis 53 0.029
561
CRY001 Cryptogenic Organizing Pneumonia 53 0.029
562
BRN038 Bronchial Disease 53 0.029
563
P HYP083 Hypopituitarism 53 0.029
564
ALC009 Alcoholic Liver Cirrhosis 53 0.029
565
c FML191 Familial Long Qt Syndrome 53 0.029
566
EXP004 Exophthalmos 52 0.029
567
PRP016 Paraplegia 52 0.029
568
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.029
569
P THY032 Thyroiditis 52 0.029
570
P MGR003 Migraine with Aura 52 0.029
571
OLG003 Oligohydramnios 51 0.029
572
MCR088 Microscopic Polyangiitis 51 0.029
573
ILS001 Ileus 51 0.029
574
THR016 Thrombophlebitis 51 0.029
575
P PRC012 Pericardial Effusion 51 0.029
576
P HYP040 Hypospadias 51 0.029
577
PNN001 Panniculitis 51 0.029
578
INT071 Intestinal Perforation 51 0.029
579
P OVR082 Overgrowth Syndrome 50 0.029
580
STT002 Status Asthmaticus 50 0.029
581
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.029
582
HRT011 Heart Septal Defect 50 0.029
583
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.029
584
AMB002 Amblyopia 49 0.029
585
c INV001 Invasive Aspergillosis 49 0.029
586
BNR002 Bone Resorption Disease 48 0.029
587
P RNV001 Renovascular Hypertension 48 0.029
588
IGG001 Iga Glomerulonephritis 48 0.029
589
HMP001 Hemopericardium 48 0.029
590
c MTR002 Mitral Valve Insufficiency 48 0.029
591
FBR032 Fibromuscular Dysplasia 48 0.029
592
HLX001 Helix Syndrome 47 0.029
593
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.029
594
HYP016 Hypochondriasis 47 0.029
595
c CHR484 Charcot-Marie-Tooth Disease, Dominant Intermediate F 47 0.029
596
AST006 Astigmatism 47 0.029
597
KHN001 Kuhnt-Junius Degeneration 47 0.029
598
P ENC008 Encephalocele 47 0.029
599
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.029
600
DPM001 Dopamine Beta-Hydroxylase Deficiency 47 0.029
601
TST044 Testicular Torsion 47 0.029
602
CYC008 Cyclic Vomiting Syndrome 47 0.029
603
RTN023 Retinitis 46 0.029
604
c ACT076 Acute Myocarditis 46 0.029
605
HYP034 Hypertensive Encephalopathy 46 0.029
606
c CHR048 Chronic Rhinitis 46 0.029
607
MTS001 Mutism 46 0.029
608
c SPL067 Split-Hand/foot Malformation 1 46 0.029
609
P ANX007 Anauxetic Dysplasia 1 46 0.029
610
OBS003 Obsessive-Compulsive Personality Disorder 46 0.029
611
GLL048 Glial Tumor 45 0.029
612
ATY001 Atypical Depressive Disorder 45 0.029
613
CYN002 Cyanosis, Transient Neonatal 45 0.029
614
P DCR003 Dacryoadenitis 45 0.029
615
THR099 Third-Degree Atrioventricular Block 45 0.029
616
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.029
617
c ERL020 Early-Onset Schizophrenia 44 0.029
618
ART012 Aortitis 44 0.029
619
CHL012 Childhood Disintegrative Disease 44 0.029
620
PRM003 Premature Ejaculation 44 0.029
621
RTN021 Retinal Vascular Occlusion 44 0.029
622
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.029
623
RFR003 Refractive Error 43 0.029
624
FNC007 Functioning Pituitary Adenoma 43 0.029
625
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.029
626
c CHR056 Chronic Tic Disorder 43 0.029
627
P AVS003 Avascular Necrosis 42 0.029
628
NRR001 Neuroretinitis 42 0.029
629
MNN002 Mononeuritis Multiplex 41 0.029
630
RST023 Resting Heart Rate, Variation in 41 0.029
631
INT025 Intermittent Explosive Disorder 41 0.029
632
LCR013 Lacrimal Duct Defect 41 0.029
633
c SCH056 Schizophrenia 15 41 0.029
634
MRP001 Morphine Dependence 41 0.029
635
RDN001 Reading Disorder 40 0.029
636
c SCN006 Secondary Syphilis 40 0.029
637
CHN002 Chancroid 40 0.029
638
INT060 Intestinal Atresia 40 0.029
639
ADS004 Aids Dementia Complex 40 0.029
640
IMM001 Immune-Complex Glomerulonephritis 40 0.029
641
P STR001 Striatonigral Degeneration 39 0.029
642
c NGH024 Night Blindness, Congenital Stationary, Type 1h 39 0.029
643
WND001 Wound Botulism 39 0.029
644
SPP007 Suppression Amblyopia 39 0.029
645
HYP344 Hyperthyroidism, Familial Gestational 39 0.029
646
OCL066 Oculogyric Crisis 38 0.029
647
SPR012 Separation Anxiety Disorder 38 0.029
648
CHL073 Cholestasis-Lymphedema Syndrome 38 0.029
649
KLP001 Kleptomania 38 0.029
650
ORB006 Orbital Cellulitis 37 0.029
651
MNN021 Meningococcemia 37 0.029
652
FNS001 Funisitis 37 0.029
653
ART010 Arteriolosclerosis 37 0.029
654
PSD088 Pseudobulbar Affect 36 0.029
655
CHM005 Chemical Colitis 35 0.029
656
AMR003 Amaurosis Fugax 34 0.029
657
P ANT001 Anterolateral Myocardial Infarction 34 0.029
658
P DCR004 Dacryocystitis 34 0.029
659
c RST012 Restless Legs Syndrome 1 34 0.029
660
HMP003 Hemopneumothorax 33 0.029
661
OVL001 Ovalocytosis, Southeast Asian 33 0.029
662
DRG001 Drug Psychosis 33 0.029
663
EPG003 Epiglottitis 33 0.029
664
PRN007 Perinephritis 33 0.029
665
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.029
666
c BLD140 Blood Group, I System 32 0.029
667
SPN012 Spindle Cell Hemangioma 32 0.029
668
SPC003 Specific Developmental Disorder 31 0.029
669
PTT010 Pituitary Infarct 31 0.029
670
PRL010 Prolactin Producing Pituitary Tumor 30 0.029
671
BRW004 Brown-Sequard Syndrome 30 0.029
672
FNT004 Fainting 30 0.029
673
CLF051 Cleft Larynx, Posterior 30 0.029
674
MTY003 Mutyh Polyposis 30 0.029
675
BSL004 Basilar Artery Occlusion 29 0.029
676
MNG003 Mungan Syndrome 29 0.029
677
MYC088 Mycobacterium Avium Complex Infections 29 0.029
678
ANT013 Anterior Spinal Artery Syndrome 29 0.029
679
PST092 Posttransplant Acute Limbic Encephalitis 29 0.029
680
P FRN011 Frontal Sinusitis 28 0.029
681
c FML169 Familial Osteochondritis Dissecans 28 0.029
682
ALC003 Alcoholic Psychosis 28 0.029
683
PMP008 Pemphigus Vegetans 27 0.029
684
LRY026 Laryngeal Cleft 27 0.029
685
MST020 Mast Cell Activation Syndrome 26 0.029
686
BNG077 Benign Idiopathic Neonatal Seizures 26 0.029
687
SPC030 Specific Language Disorder 26 0.029
688
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.029
689
c DMN005 Diamond-Blackfan Anemia 2 25 0.029
690
DRG004 Drug-Induced Mental Disorder 24 0.029
691
BLD163 Blood Group, Dombrock System 24 0.029
692
P PHC014 Phocomelia 24 0.029
693
GNT018 Gianotti Crosti Syndrome 23 0.029
694
LMB014 Limb-Body Wall Complex 22 0.029
695
PLY039 Polymorphic Reticulosis 21 0.029
696
BLD165 Blood Group, Colton System 20 0.029
697
QDR002 Quadricuspid Aortic Valve 20 0.029
698
AND005 Androgen Insensitivity Syndrome, Mild 19 0.029
699
ACT235 Acute Macular Neuroretinopathy 19 0.029
700
PNT023 Pontine Hemorrhage 17 0.029
701
NVL002 Novelty Seeking Personality Trait 16 0.029
702
P LNG032 Lung Cancer 98 0.021
703
P PRS040 Prostate Cancer 97 0.021
704
P BRS047 Breast Cancer 97 0.021
705
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.021
706
c SYS001 Systemic Lupus Erythematosus 86 0.021
707
c LKM061 Leukemia, Acute Myeloid 84 0.021
708
P PNC035 Pancreatic Cancer 84 0.021
709
c FNC027 Fanconi Anemia, Complementation Group a 81 0.021
710
P GLM040 Glioma Susceptibility 1 81 0.021
711
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.021
712
CNN003 Conn's Syndrome 79 0.021
713
c CWD006 Cowden Syndrome 1 78 0.021
714
GST019 Gastrointestinal Stromal Tumor 78 0.021
715
P LNG064 Lung Cancer Susceptibility 3 78 0.021
716
P APL001 Aplastic Anemia 74 0.021
717
c HMC039 Hemochromatosis, Type 1 74 0.021
718
P OST002 Osteoporosis 74 0.021
719
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.021
720
P RTN024 Retinoblastoma 73 0.021
721
P WSK001 Wiskott-Aldrich Syndrome 72 0.021
722
P ATS364 Autism 70 0.021
723
MYL009 Myelodysplastic Syndrome 70 0.021
724
APR006 Apert Syndrome 70 0.021
725
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.021
726
P HYP061 Hypertrophic Cardiomyopathy 70 0.021
727
P ART022 Arthritis 69 0.021
728
SVR097 Severe Cutaneous Adverse Reaction 69 0.021
729
LYM133 Lymphoma, Hodgkin, Classic 69 0.021
730
P LKM062 Leukemia, Acute Lymphoblastic 69 0.021
731
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.021
732
P CRN037 Craniosynostosis 68 0.021
733
SND001 Sandhoff Disease 68 0.021
734
c NMN015 Niemann-Pick Disease, Type C1 68 0.021
735
P ESS003 Essential Thrombocythemia 68 0.021
736
P CWD010 Cowden Syndrome 67 0.021
737
GST092 Gastroesophageal Reflux 67 0.021
738
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.021
739
BLM001 Bloom Syndrome 67 0.021
740
BRK010 Burkitt Lymphoma 67 0.021
741
ALL003 Allergic Rhinitis 67 0.021
742
P SHW006 Shwachman-Diamond Syndrome 1 67 0.021
743
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.021
744
c ATS007 Autism Spectrum Disorder 67 0.021
745
LPT001 Leptospirosis 66 0.021
746
CHD001 Chediak-Higashi Syndrome 66 0.021
747
P SKN015 Skin Carcinoma 66 0.021
748
P NSP012 Nasopharyngeal Carcinoma 66 0.021
749
c MCR129 Microvascular Complications of Diabetes 1 66 0.021
750
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.021
751
P ATR011 Atrial Fibrillation 66 0.021
752
KHL003 Kohlschutter-Tonz Syndrome 65 0.021
753
P CNJ013 Conjunctivitis 65 0.021
754
DMN031 Dementia, Lewy Body 65 0.021
755
SRC014 Sarcoma 65 0.021
756
P MTR014 Motor Neuron Disease 65 0.021
757
PRP001 Propionic Acidemia 65 0.021
758
PND002 Pendred Syndrome 65 0.021
759
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.021
760
IRR002 Irritable Bowel Syndrome 65 0.021
761
c DBT099 Diabetes Mellitus, Type I 65 0.021
762
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.021
763
P THY023 Thymoma 65 0.021
764
APN008 Apnea, Obstructive Sleep 64 0.021
765
NRM005 Neuromuscular Disease 64 0.021
766
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.021
767
BRK001 Brooke-Spiegler Syndrome 64 0.021
768
GT001 Gout 64 0.021
769
P FRD001 Friedreich Ataxia 64 0.021
770
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.021
771
LYM017 Lyme Disease 64 0.021
772
P RHB003 Rhabdomyosarcoma 63 0.021
773
c DPH024 Diaphragmatic Hernia, Congenital 63 0.021
774
LSH001 Leishmaniasis 63 0.021
775
WLK001 Walker-Warburg Syndrome 63 0.021
776
CYC010 Cyclic Neutropenia 62 0.021
777
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.021
778
P PSR002 Psoriasis 62 0.021
779
c BRN108 Branchiootic Syndrome 1 62 0.021
780
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.021
781
c NMN013 Niemann-Pick Disease, Type a 62 0.021
782
P PRP029 Porphyria 62 0.021
783
NTR005 Nutritional Deficiency Disease 62 0.021
785
P INT143 Interstitial Cystitis 61 0.021
786
NRM001 Neuromyelitis Optica 61 0.021
787
FTT001 Fatty Liver Disease 61 0.021
788
CHN055 Chanarin-Dorfman Syndrome 61 0.021
789
WST001 West Syndrome 61 0.021
790
ALV005 Alveolar Soft Part Sarcoma 61 0.021
791
RTN017 Retinal Detachment 61 0.021
792
P LPS004 Lupus Erythematosus 61 0.021
793
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.021
794
NRL005 Neurilemmoma 60 0.021
795
P MYL006 Myeloid Leukemia 60 0.021
796
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.021
797
FND001 Fundus Albipunctatus 60 0.021
798
P SCL018 Scoliosis 60 0.021
799
P TXP001 Toxoplasmosis 60 0.021
800
P VNT002 Ventricular Septal Defect 60 0.021
801
SQM006 Squamous Cell Carcinoma 60 0.021
802
P ATR010 Atrial Heart Septal Defect 60 0.021
803
RHM001 Rheumatic Fever 60 0.021
804
CHC001 Chickenpox 60 0.021
805
P PTN014 Patent Ductus Arteriosus 1 60 0.021
806
INS001 Insulinoma 60 0.021
807
STF001 Stiff-Person Syndrome 60 0.021
808
P GLY013 Glycogen Storage Disease 60 0.021
809
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 0.021
810
IGR001 Ige Responsiveness, Atopic 59 0.021
811
PRT058 Pure Autonomic Failure 59 0.021
812
GNG013 Gingivitis 59 0.021
813
ADN018 Adenoma 59 0.021
814
GST045 Gastroenteritis 59 0.021
815
HLC007 Helicobacter Pylori Infection 59 0.021
816
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.021
817
P HYP726 Hypercalcemia, Infantile, 1 58 0.021
818
c PRG018 Paragangliomas 1 58 0.021
819
HYP458 Hyper Ige Syndrome 58 0.021
820
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.021
821
ADR005 Adrenal Carcinoma 58 0.021
822
ERY003 Erythema Multiforme 58 0.021
823
P URT039 Urticaria 58 0.021
824
NWB001 Newborn Respiratory Distress Syndrome 58 0.021
825
LYM027 Lymphopenia 58 0.021
826
P CND004 Candidiasis 58 0.021
827
EXT034 Extrinsic Allergic Alveolitis 58 0.021
828
MCR013 Microphthalmia 57 0.021
829
P MYM013 Moyamoya Disease 1 57 0.021
830
MBS002 Moebius Syndrome 57 0.021
831
TRP006 Tarp Syndrome 57 0.021
832
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.021
833
BLR008 Bilirubin Metabolic Disorder 57 0.021
834
HMR039 Hemorrhage, Intracerebral 57 0.021
835
c GLC112 Galactosemia Iii 56 0.021
836
PPL058 Papilloma of Choroid Plexus 56 0.021
837
c LSS005 Lissencephaly 1 56 0.021
838
CMR002 Coumarin Resistance 56 0.021
839
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.021
840
P PLY011 Polycystic Ovary Syndrome 56 0.021
841
c ESS001 Essential Tremor 56 0.021
842
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.021
843
BCT022 Bacterial Infectious Disease 56 0.021
844
SPN041 Spinal Cord Disease 56 0.021
845
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.021
846
P PNM006 Pneumoconiosis 56 0.021
847
c GRV008 Graves Disease 1 56 0.021
848
MCS002 Mucositis 56 0.021
849
SLC006 Silicosis 56 0.021
850
P PLY019 Polyneuropathy 56 0.021
851
P AGN002 Agnosia 55 0.021
852
c FML035 Familial Hyperlipidemia 55 0.021
853
HST011 Histoplasmosis 55 0.021
854
P SCK002 Sick Sinus Syndrome 55 0.021
855
P ATR001 Atrioventricular Septal Defect 55 0.021
856
MMB001 Membranoproliferative Glomerulonephritis 55 0.021
857
c BCT007 Bacterial Meningitis 55 0.021
858
NPH009 Nephrolithiasis 55 0.021
859
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.021
860
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.021
861
P PTT006 Pituitary Adenoma 55 0.021
862
P DBT005 Diabetes Insipidus 55 0.021
863
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.021
864
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.021
865
P SLM003 Salmonellosis 55 0.021
866
HYP060 Hyperinsulinism 54 0.021
867
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 54 0.021
868
P LFT003 Left Ventricular Noncompaction 54 0.021
869
VGN023 Vaginitis 54 0.021
870
RFL001 Reflex Sympathetic Dystrophy 54 0.021
871
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.021
872
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.021
873
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.021
874
CRY003 Cryptosporidiosis 54 0.021
875
c AML044 Amelogenesis Imperfecta, Type Ig 54 0.021
876
AMN001 Amenorrhea 54 0.021
877
HMS001 Hemosiderosis 54 0.021
878
PLM012 Pulmonary Sarcoidosis 53 0.021
879
c CNT016 Central Retinal Vein Occlusion 53 0.021
880
HRT012 Heart Valve Disease 53 0.021
881
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.021
882
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.021
883
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.021
884
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.021
885
P HML001 Hemolytic-Uremic Syndrome 53 0.021
886
P ORL007 Oral Cavity Cancer 53 0.021
887
MTN003 Motion Sickness 53 0.021
888
GTR002 Goiter 53 0.021
889
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.021
890
INT075 Intracranial Hypertension 53 0.021
891
SPN035 Spindle Cell Sarcoma 53 0.021
892
ERD001 Erdheim-Chester Disease 53 0.021
893
DNT012 Dental Caries 53 0.021
894
MLN014 Melnick-Needles Syndrome 53 0.021
895
P RTN022 Retinal Vein Occlusion 53 0.021
896
c HPT007 Hepatitis E 53 0.021
897
TRC003 Trichomoniasis 53 0.021
898
c FML008 Familial Retinoblastoma 53 0.021
899
FRY006 Fryns Microphthalmia Syndrome 52 0.021
900
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.021
901
c MCR113 Microvascular Complications of Diabetes 3 52 0.021
902
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.021
903
DMY004 Demyelinating Disease 52 0.021
904
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.021
905
ACR041 Acromelic Frontonasal Dysostosis 52 0.021
906
PST011 Pustulosis of Palm and Sole 52 0.021
907
P DDN001 Duodenal Ulcer 52 0.021
908
SCH018 Schizencephaly 52 0.021
909
CRT016 Carotid Artery Disease 52 0.021
910
DYS015 Dysentery 52 0.021
911
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.021
912
c THY107 Thymoma, Familial 52 0.021
913
BWN001 Bowen-Conradi Syndrome 52 0.021
914
APR001 Apraxia 52 0.021
915
P OVR049 Ovarian Disease 52 0.021
916
PRL019 Prolidase Deficiency 52 0.021
917
LYM004 Lymphoid Interstitial Pneumonia 51 0.021
919
FCT001 Factor Viii Deficiency 51 0.021
920
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.021
921
KRT009 Keratosis 51 0.021
922
MLL018 Miller-Dieker Lissencephaly Syndrome 51 0.021
923
LNG095 Lung Abscess 51 0.021
924
c PRM108 Primary Progressive Multiple Sclerosis 51 0.021
925
CYS036 Cystinosis, Nephropathic 51 0.021
926
P LSS002 Lissencephaly 51 0.021
927
P THR015 Thrombophilia 51 0.021
928
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.021
929
BHR001 Behr Syndrome 51 0.021
930
HYP074 Hypersensitivity Vasculitis 51 0.021
931
SKN013 Skin Benign Neoplasm 51 0.021
932
RLP003 Relapsing Fever 51 0.021
933
c ACT078 Acute Porphyria 51 0.021
934
BRX001 Bruxism 50 0.021
935
RTN003 Retinal Ischemia 50 0.021
936
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.021
937
RSP006 Respiratory System Disease 50 0.021
938
BRN009 Burning Mouth Syndrome 50 0.021
939
AZS001 Azoospermia 50 0.021
940
HNT002 Hantavirus Pulmonary Syndrome 50 0.021
941
NPH018 Nephrogenic Systemic Fibrosis 50 0.021
942
ALN001 Aland Island Eye Disease 50 0.021
943
c INF145 Infantile Liver Failure Syndrome 1 50 0.021
944
ECT026 Ectopic Pregnancy 50 0.021
945
HYP748 Hypertelorism 50 0.021
946
P OMP004 Omphalocele 50 0.021
947
NPH010 Nephrosclerosis 50 0.021
948
HYP080 Hypogonadism 50 0.021
949
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.021
950
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 49 0.021
951
PPL021 Papilledema 49 0.021
952
P IGN003 Iga Nephropathy 1 49 0.021
953
SYS003 Systolic Heart Failure 49 0.021
954
P CRV039 Cervicitis 49 0.021
955
P END046 Endometritis 49 0.021
956
CRP032 Corpus Callosum, Agenesis of 49 0.021
957
SNT005 Sinoatrial Node Disease 49 0.021
958
INT078 Intracranial Thrombosis 49 0.021
959
TRT020 Tritanopia 49 0.021
960
MNN009 Meningoencephalitis 49 0.021
961
c SPN330 Spondylocostal Dysostosis 5 49 0.021
962
SPN405 Spondyloepiphyseal Dysplasia Tarda, X-Linked 49 0.021
963
VCC001 Vaccinia 49 0.021
964
MLR002 Miliary Tuberculosis 49 0.021
965
RYN001 Raynaud Disease 48 0.021
966
c BCT013 Bacterial Pneumonia 48 0.021
967
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.021
968
ADT003 Auditory System Disease 48 0.021
969
CRY004 Cryoglobulinemia 48 0.021
970
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.021
971
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.021
972
P PRN026 Porencephaly 48 0.021
973
CLS016 Clostridium Difficile Colitis 48 0.021
974
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.021
975
GLC106 Glucocorticoid Resistance, Generalized 48 0.021
976
PTT004 Pituitary Apoplexy 48 0.021
977
BNN003 Bone Inflammation Disease 48 0.021
978
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.021
979
P SLL003 Salla Disease 48 0.021
980
CHL056 Cheilitis 48 0.021
981
MDD010 Middle Ear Disease 48 0.021
982
c HYD064 Hydrocephalus, Congenital, 1 48 0.021
983
P TRT019 Torticollis 48 0.021
984
P MRC003 Mercury Poisoning 48 0.021
985
ANT018 Anthracosis 48 0.021
986
MCR018 Microcytic Anemia 47 0.021
987
DRY001 Dry Eye Syndrome 47 0.021
988
MCC002 Mucocutaneous Leishmaniasis 47 0.021
989
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 47 0.021
990
KRT008 Keratopathy 47 0.021
991
c MCR120 Microvascular Complications of Diabetes 7 47 0.021
992
STR089 Storage Pool Platelet Disease 47 0.021
993
WRN003 Wernicke Encephalopathy 47 0.021
994
c CNG216 Congenital Hydrocephalus 47 0.021
995
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.021
996
P OVR046 Ovarian Cyst 47 0.021
997
c CNT075 Central Precocious Puberty 46 0.021
998
c KNB006 Knobloch Syndrome 1 46 0.021
999
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.021
1000
LCK001 Locked-in Syndrome 46 0.021
1001
ORC001 Orchitis 46 0.021
1002
FCL012 Facial Paralysis 46 0.021
1003
EXS001 Exostosis 46 0.021
1004
KRT013 Keratolytic Winter Erythema 46 0.021
1005
P BRB001 Beriberi 46 0.021
1006
PLY012 Polyhydramnios 46 0.021
1007
NSD001 Nose Disease 46 0.021
1008
HYD005 Hydrocele 46 0.021
1009
c SCH079 Schizophrenia 1 46 0.021
1010
CWP001 Cowpox 46 0.021
1011
RMS001 Rem Sleep Behavior Disorder 46 0.021
1012
PST027 Postencephalitic Parkinson Disease 46 0.021
1013
NRS003 Neurosyphilis 45 0.021
1014
HPT004 Hepatic Coma 45 0.021
1015
c CNT015 Central Sleep Apnea 45 0.021
1016
c SPN097 Spinocerebellar Ataxia 23 45 0.021
1017
MLK003 Melkersson-Rosenthal Syndrome 45 0.021
1018
SYN005 Synostosis 45 0.021
1020
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 45 0.021
1021
P PRD021 Periodic Paralysis 45 0.021
1022
P OSS001 Ossifying Fibroma 45 0.021
1023
HMH004 Hemihyperplasia, Isolated 45 0.021
1024
ASP008 Aspiration Pneumonitis 45 0.021
1025
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.021
1026
SPS057 Spasticity 45 0.021
1027
RTR001 Retrograde Amnesia 44 0.021
1028
CNT046 Central Nervous System Vasculitis 44 0.021
1029
P PRS062 Persistent Hyperplastic Primary Vitreous 44 0.021
1030
CRD003 Cardiac Sarcoidosis 44 0.021
1031
LTH001 Lethal Midline Granuloma 44 0.021
1032
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.021
1033
c PCH010 Pachyonychia Congenita 3 44 0.021
1034
IRT001 Iritis 44 0.021
1035
P PRL003 Proliferative Glomerulonephritis 44 0.021
1036
PRT011 Protein C Deficiency 44 0.021
1037
CRN045 Corneal Dystrophy and Perceptive Deafness 44 0.021
1038
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.021
1039
CRP002 Croup 44 0.021
1040
SCT002 Scotoma 44 0.021
1041
PPL001 Papillary Adenoma 44 0.021
1042
PKL001 Poikiloderma with Neutropenia 44 0.021
1043
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.021
1044
PRT014 Protein S Deficiency 44 0.021
1045
HPT082 Hepatic Adenomas, Familial 44 0.021
1046
FBR054 Fibroma 44 0.021
1047
FNG004 Fungal Meningitis 44 0.021
1048
CRB090 Cerebral Hypoxia 44 0.021
1049
HYP791 Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate 43 0.021
1050
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 43 0.021
1051
SDD008 Sudden Sensorineural Hearing Loss 43 0.021
1052
P PRP034 Purpura Fulminans 43 0.021
1053
HMP009 Haemophilus Influenzae 43 0.021
1054
P GRN010 Granular Cell Tumor 42 0.021
1055
ALC010 Alcoholic Cardiomyopathy 42 0.021
1056
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.021
1057
PHH001 Phaeohyphomycosis 42 0.021
1058
KLN009 Kleine-Levin Hibernation Syndrome 42 0.021
1059
P LBY004 Labyrinthitis 42 0.021
1060
ORB013 Orbital Disease 42 0.021
1061
EPT021 Epithelial Recurrent Erosion Dystrophy 42 0.021
1062
INT276 Interatrial Communication 42 0.021
1063
MLT084 Multicystic Dysplastic Kidney 42 0.021
1064
OBS082 Obstructive Nephropathy 42 0.021
1065
GST020 Gastric Antral Vascular Ectasia 41 0.021
1066
CNG134 Congenitally Corrected Transposition of the Great Arteries 41 0.021
1067
P KLZ004 Kala-Azar 1 41 0.021
1068
LTX001 Latex Allergy 41 0.021
1069
WCK001 Wieacker-Wolff Syndrome 41 0.021
1070
49X006 49, Xxxxy Syndrome 41 0.021
1071
c MCR130 Microvascular Complications of Diabetes 6 41 0.021
1072
c MCR133 Microvascular Complications of Diabetes 4 41 0.021
1073
PHB003 Phobia, Specific 41 0.021
1074
ASY002 Asymptomatic Neurosyphilis 41 0.021
1075
P BLL007 Bullous Skin Disease 41 0.021
1076
c MCR112 Microvascular Complications of Diabetes 2 41 0.021
1077
BDY001 Body Dysmorphic Disorder 40 0.021
1078
HPR006 Heparin Cofactor Ii Deficiency 40 0.021
1079
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.021
1080
HYP030 Hypoactive Sexual Desire Disorder 40 0.021
1081
ACT093 Actinic Cheilitis 40 0.021
1082
RTR011 Retroperitoneal Fibrosis 40 0.021
1083
ADJ001 Adjustment Disorder 40 0.021
1084
KLD004 Keloid Disorder 40 0.021
1085
PRM024 Primary Angle-Closure Glaucoma 40 0.021
1086
P ARC016 Auriculocondylar Syndrome 1 39 0.021