Search results for Cocaine

1620 hits were found for Cocaine

# Family MCID Name MIFTS Score
1
CCN002 Cocaine Abuse 49 75.470
2
CCN001 Cocaine Dependence 47 70.808
3
CCN009 Cocaine Intoxication 30 37.632
4
CCN012 Cocaine Antenatal Exposure 14 32.529
5
CCN010 Cocaine Embryofetopathy 13 26.802
6
P SBS003 Substance Abuse 54 19.464
7
ALC007 Alcohol Dependence 65 12.503
8
DRG003 Drug Dependence 46 11.382
9
OPT003 Opiate Dependence 49 10.892
10
P ALC033 Alcohol Use Disorder 67 10.830
11
P ATT013 Attention Deficit-Hyperactivity Disorder 65 9.769
12
PSY004 Psychotic Disorder 66 9.222
13
P PRS038 Personality Disorder 65 9.126
14
P VSC011 Vasculitis 61 8.362
15
SBS004 Substance Dependence 46 7.837
17
P SZR006 Seizure Disorder 69 7.320
18
OPD006 Opioid Addiction 48 6.696
19
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 6.683
20
OPD001 Opioid Abuse 44 6.590
21
MNT002 Mental Depression 56 6.393
22
PLY068 Polysubstance Abuse 41 6.261
23
PST028 Post-Traumatic Stress Disorder 58 6.197
24
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 6.056
25
DPR016 Depression 64 6.017
26
P BPL003 Bipolar Disorder 56 5.977
27
WTH001 Withdrawal Disorder 47 5.786
28
c MJR022 Major Affective Disorder 8 37 5.785
29
c MJR024 Major Affective Disorder 9 40 5.785
30
ANT011 Antisocial Personality Disorder 47 5.665
31
ANX010 Anxiety 70 5.595
32
MDD011 Mood Disorder 61 5.544
33
AVD001 Avoidant Personality Disorder 49 5.543
34
TBC004 Tobacco Addiction 63 5.473
35
ISC004 Ischemia 61 5.453
36
HRN003 Heroin Dependence 44 5.441
37
ART074 Aortic Dissection 53 5.246
38
P SYP003 Syphilis 59 5.215
39
PLC007 Placental Abruption 47 5.181
40
P MJR001 Major Depressive Disorder 68 5.098
41
GRN017 Granulocytopenia 42 5.062
42
c ACT071 Acute Kidney Failure 60 4.930
43
SBC016 Subacute Delirium 42 4.866
44
CRD132 Cardiac Conduction Defect 59 4.780
45
P SCH015 Schizophrenia 74 4.771
46
PRP030 Purpura 54 4.747
47
P MYC008 Myocarditis 59 4.745
48
P SMK004 Smoking As a Quantitative Trait Locus 3 44 4.643
49
c ACT075 Acute Myocardial Infarction 55 4.576
50
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.559
51
P MYC007 Myocardial Infarction 69 4.539
52
ACQ007 Acquired Immunodeficiency Syndrome 58 4.538
53
ACT084 Acute Stress Disorder 53 4.390
54
CNN001 Cannabis Dependence 37 4.377
55
IMM167 Immune Deficiency Disease 76 4.347
56
LPP008 Lipoprotein Quantitative Trait Locus 65 4.341
57
P EXN002 Exanthem 58 4.299
58
DSS008 Disease of Mental Health 74 4.171
59
P NTR004 Neutropenia 62 4.156
60
PLM010 Pulmonary Edema 54 4.140
61
P KDN018 Kidney Disease 71 4.127
62
CRN019 Coronary Artery Vasospasm 47 4.113
63
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 4.100
64
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 4.091
65
P TRM003 Tremor 50 3.950
66
SDD001 Sudden Infant Death Syndrome 60 3.869
67
48X005 48,xyyy 39 3.818
68
SVR004 Severe Combined Immunodeficiency 70 3.816
69
P CRD119 Cardiac Arrest 68 3.804
70
HMN044 Human Immunodeficiency Virus Type 1 76 3.761
71
CNN002 Cannabis Abuse 44 3.649
72
c DLT002 Dilated Cardiomyopathy 79 3.623
73
c HPT001 Hepatitis C 61 3.621
74
P VSC007 Vascular Disease 62 3.603
75
STT001 Status Epilepticus 58 3.584
76
PNM008 Pneumothorax 54 3.488
77
THR024 Thrombosis 56 3.486
78
PNG002 Pain Agnosia 51 3.481
79
P HDC001 Headache 56 3.477
80
ANG054 Angina Pectoris 65 3.382
81
P GLM007 Glomerulonephritis 59 3.364
82
ETN001 Eating Disorder 59 3.349
83
P PRK057 Parkinson Disease, Late-Onset 79 3.308
84
CRB039 Cerebrovascular Disease 65 3.306
85
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.306
86
CND002 Conduct Disorder 50 3.165
87
P MCR010 Microcephaly 59 3.164
88
PTH002 Pathological Gambling 48 3.160
89
AGN016 Aging 53 3.142
90
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.119
91
P HPT021 Hepatitis 68 3.087
92
OBS002 Obsessive-Compulsive Disorder 67 3.083
93
BRN071 Brain Injury 50 3.064
94
ART140 Arteries, Anomalies of 52 3.060
95
P PRK039 Parkinsonism 55 3.035
96
c ATR087 Atrial Standstill 1 74 3.026
97
P PLM037 Pulmonary Hypertension 69 3.020
98
HYP020 Hyperprolactinemia 63 3.018
99
P DYS154 Dystonia 64 2.978
100
CRN017 Coronary Thrombosis 46 2.964
101
DSS032 Disease by Infectious Agent 55 2.908
102
GRN037 Granulomatosis with Polyangiitis 66 2.905
103
c HPT073 Hepatitis C Virus 70 2.894
104
TRM010 Traumatic Brain Injury 50 2.893
105
CNG034 Congestive Heart Failure 69 2.884
106
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.883
107
ENT011 Enterocolitis 55 2.866
108
THR123 Thrombotic Microangiopathy 40 2.816
109
CHL014 Cholera 62 2.813
110
ANR040 Aneurysm 60 2.807
111
AMP007 Amphetamine Abuse 36 2.790
112
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 2.749
113
ART002 Arts Syndrome 66 2.748
114
P CHR345 Chronic Pain 50 2.739
115
ISC015 Ischemic Colitis 43 2.729
116
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.711
117
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.711
118
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.711
119
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.711
120
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.711
121
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.711
122
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.711
123
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.711
124
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.711
125
PRN019 Perinatal Necrotizing Enterocolitis 60 2.709
126
P FTL001 Fetal Alcohol Syndrome 55 2.696
127
47X002 47,xyy 47 2.695
128
c BPL002 Bipolar I Disorder 47 2.684
129
P END033 Endocarditis 58 2.675
130
P PNC025 Panic Disorder 52 2.674
131
CYT002 Cytokine Deficiency 43 2.667
132
PYD002 Pyoderma 49 2.628
133
PYD001 Pyoderma Gangrenosum 53 2.628
134
DYS073 Dysphagia 53 2.607
135
P THR014 Thrombocytopenia 66 2.600
136
BRD004 Borderline Personality Disorder 53 2.581
137
CLT003 Colitis 63 2.574
138
SCH012 Schizoaffective Disorder 49 2.573
139
P CNJ013 Conjunctivitis 66 2.561
140
INT067 Interstitial Nephritis 46 2.541
141
SXL003 Sexual Disorder 49 2.532
142
P MVM001 Movement Disease 61 2.520
143
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.509
144
P ALZ034 Alzheimer Disease 87 2.466
145
P ENC018 Encephalopathy 62 2.458
146
NNT008 Neonatal Abstinence Syndrome 41 2.457
147
END086 End Stage Renal Disease 54 2.451
148
STR067 Stroke, Ischemic 79 2.435
149
P AST005 Asthma 75 2.419
150
c MLG069 Malignant Hypertension 46 2.413
151
P CLS010 Cluster Headache 42 2.399
152
P HRN001 Horner's Syndrome 45 2.384
153
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.363
154
IRN002 Iron Metabolism Disease 56 2.361
155
P SLP005 Sleep Disorder 61 2.359
156
c HYP595 Hypertension, Essential 84 2.350
157
DYS009 Dysthymic Disorder 51 2.324
158
c PRC016 Pre-Eclampsia 64 2.323
159
c CNG033 Congenital Syphilis 39 2.322
160
P PHC003 Pheochromocytoma 70 2.311
161
ADR040 Adrenal Gland Pheochromocytoma 45 2.311
162
CRN030 Coronary Stenosis 50 2.307
163
ADL002 Adult Syndrome 69 2.305
164
OCL069 Ocular Motor Apraxia 57 2.298
165
PRP007 Priapism 46 2.292
166
P MJR007 Major Affective Disorder 1 42 2.285
167
DBT084 Diabetes Mellitus, Ketosis-Prone 59 2.273
168
P RHN004 Rhinitis 56 2.269
169
HYP264 Hypertonia 35 2.256
170
DFF031 Diffuse Alveolar Hemorrhage 31 2.233
171
P NRC002 Narcolepsy 55 2.232
172
PRT037 Pertussis 49 2.210
173
P HYP076 Hyperthyroidism 53 2.193
174
c MGR028 Migraine with or Without Aura 1 63 2.185
175
P RSP003 Respiratory Failure 73 2.185
176
PLC008 Placenta Disease 48 2.179
177
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.174
178
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.166
179
c CHR684 Chronic Kidney Disease 73 2.163
180
c PNS012 Paine Syndrome 60 2.160
181
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.160
182
P NRB001 Neuroblastoma 66 2.158
183
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.149
184
NRL004 Neuroleptic Malignant Syndrome 52 2.134
185
AGR002 Agoraphobia 45 2.112
186
P ART005 Arteriovenous Malformation 64 2.086
187
P BRG001 Brugada Syndrome 69 2.072
188
PLM033 Pulmonary Embolism 58 2.072
189
CRS001 Crescentic Glomerulonephritis 42 2.068
190
c MJR006 Major Affective Disorder 5 32 2.065
191
c MJR003 Major Affective Disorder 6 32 2.065
193
ANC002 Anca-Associated Vasculitis 44 2.056
194
P OPT006 Optic Nerve Disease 57 2.040
195
SCH003 Schizophreniform Disorder 54 2.040
196
AMN003 Amnestic Disorder 53 2.037
197
ANR007 Anorexia Nervosa 59 2.032
198
OPP004 Oppositional Defiant Disorder 48 2.032
199
P TCD001 Tic Disorder 50 2.021
200
MTB004 Metabolic Acidosis 48 2.020
201
SYN036 Syncope 44 2.018
202
END040 Endogenous Depression 54 2.012
203
ACT011 Acute Contagious Conjunctivitis 41 2.000
204
RCK004 Rickets 64 1.979
205
ALL029 Allergic Disease 61 1.976
206
c MJR008 Major Affective Disorder 2 34 1.976
207
c MJR023 Major Affective Disorder 7 33 1.976
208
c MJR004 Major Affective Disorder 4 28 1.976
209
GNR004 Generalized Anxiety Disorder 54 1.974
210
LPD008 Lipid Metabolism Disorder 61 1.958
211
P PNC044 Pancreatitis 61 1.958
212
RYN005 Raynaud Phenomenon 45 1.954
213
HYP056 Hypoglycemia 65 1.946
214
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.945
215
CRD137 Cardiogenic Shock 56 1.939
216
DFC004 Deficiency Anemia 74 1.928
217
KRT019 Keratitis, Hereditary 66 1.927
218
P ANR048 Aniridia 1 66 1.918
219
SCL003 Social Phobia 48 1.916
220
AND005 Androgen Insensitivity Syndrome, Mild 21 1.902
221
P ANT006 Antiphospholipid Syndrome 55 1.902
222
ATM095 Autoimmune Disease 61 1.901
223
c ACT027 Acute Pancreatitis 60 1.888
224
PRT036 Peritonitis 65 1.875
225
ATH013 Atherosclerosis Susceptibility 63 1.875
226
CLL003 Cellulitis 53 1.875
227
NRT001 Neurotic Disorder 56 1.871
228
ALX002 Alexithymia 36 1.867
229
P MYC084 Mycobacterium Tuberculosis 1 68 1.858
230
P HRT032 Heart Disease 84 1.857
231
ATR057 Atrioventricular Block 54 1.848
232
CHL123 Chlamydia 58 1.847
233
CRD223 Cardiac Arrhythmia 63 1.842
234
PNM010 Pneumothorax, Primary Spontaneous 58 1.840
235
c ACT134 Acute Liver Failure 57 1.827
236
P ECL001 Eclampsia 52 1.824
237
LMB062 Limb Ischemia 55 1.815
238
RTN020 Retinal Vascular Disease 45 1.815
239
TRN015 Transient Cerebral Ischemia 62 1.813
240
P NRP001 Neuropathy 59 1.806
241
P SLP006 Sleep Apnea 69 1.799
242
OST017 Osteomyelitis 63 1.789
243
LNG099 Lung Disease 62 1.777
244
SBS005 Substance-Induced Psychosis 31 1.773
245
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.772
246
SPN185 Spinal Cord Infarction 28 1.747
247
ACT003 Acute Kidney Tubular Necrosis 46 1.733
248
PHB001 Phobic Disorder 45 1.720
249
HMP005 Hemiplegia 53 1.708
250
c HPT016 Hepatitis B 62 1.690
251
IMP006 Impulse Control Disorder 44 1.688
252
c HYP836 Hypercholesterolemia, Familial, 1 73 1.685
253
P STR020 Strabismus 56 1.667
254
MCH006 Mechanical Strabismus 40 1.667
255
BRN002 Bronchiolitis 57 1.655
256
ANS021 Anisocoria 24 1.649
257
P SYS005 Systemic Scleroderma 73 1.647
258
CRN270 Coronary Artery Dissection, Spontaneous 33 1.645
259
P ART021 Arteriosclerosis 53 1.645
260
CYC005 Cyclothymic Disorder 40 1.644
261
BRN026 Branch Retinal Artery Occlusion 41 1.636
262
P RTN014 Retinal Artery Occlusion 46 1.636
263
NRL016 Neural Tube Defects 80 1.636
264
INT051 Intussusception 53 1.627
265
c HPT003 Hepatitis a 63 1.626
266
HDN002 Head Injury 44 1.625
267
MTR086 Motor Stereotypies 14 1.624
268
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.624
269
BRN012 Bronchiolitis Obliterans 56 1.624
270
P HYP263 Hypersomnia 40 1.609
271
PMP006 Pemphigus Vulgaris, Familial 57 1.604
272
P PMP001 Pemphigus 54 1.604
273
P HYP098 Hypereosinophilic Syndrome 66 1.603
274
c VRL010 Viral Hepatitis 52 1.593
275
TTN003 Tetanus 64 1.593
276
GSG001 Gas Gangrene 52 1.590
277
HYP266 Hypoxia 56 1.586
278
P SCK005 Sickle Cell Disease 56 1.584
279
SRT004 Serotonin Syndrome 54 1.584
280
DSS009 Disseminated Intravascular Coagulation 56 1.579
281
P ADL010 Adult Respiratory Distress Syndrome 70 1.577
282
PST021 Postpartum Depression 50 1.570
283
P PNM007 Pneumonia 64 1.559
284
HYP066 Hyperglycemia 60 1.551
285
P LNG028 Long Qt Syndrome 63 1.544
286
CLF027 Cleft Palate, Isolated 64 1.543
287
TXC002 Toxic Encephalopathy 51 1.542
288
PRN009 Paranoid Schizophrenia 49 1.536
289
ORB013 Orbital Disease 42 1.532
290
P HYP265 Hypotonia 42 1.525
291
SPC010 Speech and Communication Disorders 47 1.515
293
P HRP006 Herpes Simplex 65 1.513
294
FDB001 Foodborne Botulism 55 1.508
295
P MYG005 Myoglobinuria 40 1.507
296
P MTH007 Methemoglobinemia 46 1.504
297
CRB086 Cerebral Aneurysms 40 1.499
298
ART016 Aortic Aneurysm 68 1.486
299
P HYD006 Hydrocephalus 62 1.486
300
INF034 Infective Endocarditis 53 1.485
301
PRT082 Preterm Premature Rupture of the Membranes 56 1.481
302
P MMB011 Membranous Nephropathy 50 1.481
303
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.479
304
LRN003 Learning Disability 49 1.479
305
P INT070 Intestinal Obstruction 57 1.475
306
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.469
307
PRP027 Peripheral Vascular Disease 71 1.463
308
BCK006 Back Pain 43 1.462
309
RBS001 Rabies 57 1.458
310
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.458
311
PLC009 Placenta Praevia 39 1.458
312
INT007 Intermediate Coronary Syndrome 53 1.458
313
CLF001 Cleft Lip 54 1.456
314
P CRB088 Cerebral Atrophy 32 1.456
315
P HYP086 Hypothyroidism 68 1.455
316
P CMP008 Compartment Syndrome 49 1.451
317
GLB002 Glioblastoma 67 1.446
318
P PRD008 Periodontitis 63 1.443
319
P DRR001 Diarrhea 55 1.441
320
CNT028 Central Retinal Artery Occlusion 42 1.431
321
INT071 Intestinal Perforation 49 1.429
322
CNS004 Constipation 56 1.427
323
c ACT249 Acute Asthma 40 1.424
324
P LVR013 Liver Disease 68 1.422
325
DLS001 Delusional Disorder 44 1.420
326
P HNT016 Huntington Disease 73 1.417
327
c THR092 Thrombophilia Due to Thrombin Defect 74 1.417
328
KRN002 Kearns-Sayre Syndrome 62 1.415
329
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.413
330
P TRN020 Turner Syndrome 67 1.413
331
HRW001 Hair Whorl 35 1.404
332
TXC005 Toxic Shock Syndrome 61 1.404
333
VLV047 Volvulus of Midgut 55 1.401
334
MRP001 Morphine Dependence 41 1.392
335
BLM002 Bulimia Nervosa 56 1.390
336
ATN005 Autonomic Dysfunction 45 1.390
337
ORL011 Oral Cancer 60 1.388
338
P GLM040 Glioma Susceptibility 1 70 1.386
339
MLG169 Malignant Astrocytoma 57 1.386
340
P CRN028 Corneal Ulcer 47 1.383
341
P ACT028 Acute Closed-Angle Glaucoma 32 1.365
342
P CRN074 Coronary Artery Aneurysm 41 1.363
343
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.352
344
IRN001 Iron Deficiency Anemia 58 1.352
345
c DRR009 Diarrhea 6 46 1.351
346
c PRM038 Primary Agammaglobulinemia 47 1.351
347
PLG002 Plague 58 1.347
348
IMP005 Impotence 52 1.346
349
FRN014 Fournier Gangrene 26 1.340
350
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.333
351
P LTR001 Lateral Sclerosis 57 1.333
352
BLC015 Balo Concentric Sclerosis 37 1.327
353
CRT008 Carotid Artery Dissection 29 1.326
354
P MGR001 Migraine Without Aura 48 1.316
355
INT030 Intracranial Aneurysm 55 1.314
356
c ATM104 Autoimmune Vasculitis 37 1.307
357
P MYS003 Myasthenia Gravis 67 1.301
358
MSC007 Muscle Hypertrophy 64 1.301
359
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.301
360
TRG002 Trigeminal Neuralgia 61 1.300
361
OST003 Osteonecrosis 60 1.300
362
QDR001 Quadriplegia 49 1.286
363
LPT014 Leptin Deficiency or Dysfunction 77 1.286
364
MLN003 Melancholia 41 1.286
365
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.286
366
PHN011 Phenytoin Toxicity 32 1.286
367
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 1.286
368
PPT005 Peptic Ulcer Disease 58 1.286
369
P ENC004 Encephalitis 61 1.284
370
EPT021 Epithelial Recurrent Erosion Dystrophy 45 1.277
371
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 1.277
372
ATX019 Ataxia with Vitamin E Deficiency 44 1.277
373
P ESN008 Eosinophilic Pneumonia 50 1.276
374
PRV004 Periventricular Leukomalacia 52 1.275
375
c SCL052 Scleroderma, Familial Progressive 60 1.270
376
SSC001 Susac Syndrome 32 1.270
377
TRD006 Tardive Dyskinesia 53 1.270
378
BRN018 Borna Disease 36 1.270
379
P PTS002 Ptosis 52 1.260
380
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.258
381
P MLG056 Malignant Hyperthermia 65 1.258
382
P ART022 Arthritis 70 1.254
383
P AVS003 Avascular Necrosis 41 1.254
384
ANX004 Anoxia 40 1.253
385
FBR047 Fibromyalgia 57 1.252
386
DPH001 Diphtheria 59 1.240
387
P ASP006 Aspergillosis 71 1.236
388
MNN017 Mononeuropathy 41 1.236
389
HYP005 Hypokalemia 55 1.236
390
CLF004 Cleft Lip/palate 56 1.236
391
c CNT035 Central Nervous System Disease 53 1.233
392
FTL006 Fetal Alcohol Spectrum Disorder 43 1.231
393
CHR005 Chorioamnionitis 50 1.231
394
P RPD001 Rapidly Progressive Glomerulonephritis 43 1.230
395
HYD002 Hydronephrosis 58 1.230
396
PCM002 Pauci-Immune Glomerulonephritis 33 1.230
397
INT042 Internuclear Ophthalmoplegia 32 1.217
398
INT002 Intermittent Claudication 61 1.213
399
SPN186 Spinal Cord Injury 60 1.213
400
SPR012 Separation Anxiety Disorder 41 1.212
401
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.211
402
RGH001 Right Bundle Branch Block 47 1.211
403
CHR074 Choriocarcinoma 46 1.211
404
PHB003 Phobia, Specific 44 1.207
405
PNM001 Pneumocystosis 60 1.196
406
GST009 Gastroschisis 53 1.192
407
ABD010 Abdominal Wall Defect 37 1.192
408
BRK012 Broken Heart Syndrome 42 1.190
409
HRT011 Heart Septal Defect 49 1.184
410
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.180
411
P MYC033 Myoclonus 46 1.180
412
P BRN022 Bronchiectasis 59 1.176
413
NCR003 Necrotizing Sialometaplasia 29 1.172
414
LMB014 Limb-Body Wall Complex 30 1.172
415
P SNS001 Sensorineural Hearing Loss 60 1.169
416
P SRC025 Sarcoidosis 1 70 1.167
417
ARG004 Argyria 26 1.167
418
STT041 Stuttering 52 1.160
419
ADS004 Aids Dementia Complex 39 1.159
420
GNT003 Genital Herpes 54 1.157
421
INT066 Interstitial Lung Disease 60 1.154
423
P MYP004 Myopathy 67 1.149
424
APH002 Aphasia 55 1.146
425
SCK003 Sickle Cell Anemia 74 1.146
426
P EPL164 Epilepsy 70 1.146
427
BRN024 Bronchitis 67 1.144
428
P HML002 Hemolytic Anemia 62 1.134
429
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.133
430
ORC001 Orchitis 43 1.132
431
FBR032 Fibromuscular Dysplasia 41 1.132
432
P RNL015 Renal Hypertension 45 1.122
433
PHN001 Phencyclidine Abuse 23 1.121
434
CPG001 Capgras Syndrome 26 1.117
435
P DCR003 Dacryoadenitis 44 1.117
436
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.117
437
BRN004 Brain Edema 54 1.112
438
c ACT068 Acute Cystitis 60 1.112
439
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.112
440
BRN056 Bronchopulmonary Dysplasia 57 1.102
441
LVR012 Liver Cirrhosis 62 1.102
442
PRX097 Paroxysmal Dystonia 32 1.102
443
ASP007 Aspiration Pneumonia 49 1.092
444
c ACR088 Aicardi-Goutieres Syndrome 3 39 1.092
445
SPL018 Splenomegaly 47 1.092
446
P FBR031 Febrile Seizures 52 1.092
447
RFR003 Refractive Error 41 1.091
448
STT002 Status Asthmaticus 49 1.086
449
P DCR004 Dacryocystitis 36 1.086
450
SKN016 Skin Disease 63 1.082
451
OTT002 Otitis Media 70 1.076
452
LCR013 Lacrimal Duct Defect 40 1.068
453
P DMN002 Dementia 65 1.068
454
P ENC008 Encephalocele 46 1.068
455
c TYP009 Type 2 Diabetes Mellitus 91 1.061
456
CRB009 Cerebritis 43 1.061
457
PLC006 Placental Choriocarcinoma 38 1.060
458
c SPL067 Split-Hand/foot Malformation 1 46 1.049
459
PTT010 Pituitary Infarct 32 1.049
460
ORB006 Orbital Cellulitis 38 1.049
461
HPT019 Hepatic Encephalopathy 59 1.049
462
PNC129 Pancreatic Adenocarcinoma 64 1.049
463
OBS003 Obsessive-Compulsive Personality Disorder 43 1.049
464
P RTT002 Rett Syndrome 79 1.049
465
c EXD008 Exudative Vitreoretinopathy 1 71 1.049
466
PTH003 Pathologic Nystagmus 52 1.049
467
CHL012 Childhood Disintegrative Disease 44 1.034
468
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.030
469
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 1.030
470
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 1.030
471
c BLD140 Blood Group, I System 47 1.030
472
c FNC043 Fanconi Anemia, Complementation Group E 62 1.030
473
WND001 Wound Botulism 34 1.028
474
CHR001 Churg-Strauss Syndrome 61 1.028
475
CMM005 Common Cold 55 1.028
476
P PHC014 Phocomelia 23 1.028
477
PMP008 Pemphigus Vegetans 27 1.028
478
HND015 Hand Skill, Relative 29 1.025
479
SCH011 Schizotypal Personality Disorder 36 1.025
480
PRP009 Peripartum Cardiomyopathy 54 1.018
481
GST023 Gastric Ulcer 52 1.012
482
P LCT001 Lactic Acidosis 50 1.012
483
SPL006 Splenic Infarction 37 1.011
484
P MLT020 Multiple Sclerosis 79 1.008
485
SPT006 Septooptic Dysplasia 62 1.004
486
GLC096 Galactorrhea 40 1.004
487
P RNL100 Renal Hypodysplasia/aplasia 1 63 1.004
488
CNN005 Connective Tissue Disease 66 1.004
489
BRN038 Bronchial Disease 51 1.004
490
MTS001 Mutism 44 1.004
491
PST011 Pustulosis of Palm and Sole 52 1.004
492
ALG001 Algoneurodystrophy 37 1.004
493
P OPT009 Optic Neuritis 57 1.004
494
ART012 Aortitis 41 1.004
495
P PSR002 Psoriasis 63 1.004
496
HRP004 Herpes Zoster 60 1.004
497
P RNL123 Renal Agenesis, Bilateral 37 1.004
498
GNG003 Gingival Recession 50 0.999
499
MLD018 Mild Cognitive Impairment 48 0.997
500
SPP007 Suppression Amblyopia 38 0.987
501
AMB002 Amblyopia 49 0.987
502
c SVR005 Severe Pre-Eclampsia 49 0.985
503
GLL008 Gilles De La Tourette Syndrome 64 0.984
504
CHM005 Chemical Colitis 34 0.976
505
ANG020 Angiosarcoma 63 0.976
506
TST044 Testicular Torsion 45 0.976
507
INV001 Invasive Aspergillosis 48 0.976
508
INT025 Intermittent Explosive Disorder 39 0.976
509
THR016 Thrombophlebitis 50 0.976
510
SPT004 Septic Arthritis 58 0.976
511
HYP034 Hypertensive Encephalopathy 43 0.976
512
MCR141 Mucormycosis 59 0.976
513
c SCN006 Secondary Syphilis 36 0.973
514
P DBT009 Diabetes Mellitus 67 0.972
515
CRB004 Cerebral Artery Occlusion 45 0.971
516
GT001 Gout 63 0.963
517
INF013 Inferior Myocardial Infarction 33 0.955
518
ANR004 Anuria 44 0.955
519
PLR007 Pleural Empyema 50 0.955
520
PRT251 Proteinuria, Chronic Benign 58 0.953
521
P NPH012 Nephrotic Syndrome 61 0.953
522
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.953
523
BNG077 Benign Idiopathic Neonatal Seizures 23 0.953
524
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.942
525
P ORT004 Orthostatic Intolerance 61 0.942
526
P FCL005 Focal Segmental Glomerulosclerosis 57 0.942
527
PSD088 Pseudobulbar Affect 33 0.942
528
CRY001 Cryptogenic Organizing Pneumonia 53 0.939
529
ALC006 Alcoholic Hepatitis 61 0.939
530
ALC009 Alcoholic Liver Cirrhosis 54 0.939
531
BRW004 Brown-Sequard Syndrome 31 0.939
532
P CTR002 Cataract 59 0.938
533
P CRD246 Cardiovascular System Disease 55 0.936
534
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.936
535
PHR003 Pharyngitis 57 0.935
536
P URN019 Urinary Tract Infection 48 0.931
537
c DMN005 Diamond-Blackfan Anemia 2 28 0.920
538
FNS001 Funisitis 36 0.920
539
DNT012 Dental Caries 53 0.920
540
ANG005 Anogenital Venereal Wart 55 0.920
541
GLM045 Glioma 62 0.920
542
GLL048 Glial Tumor 51 0.920
543
THR099 Third-Degree Atrioventricular Block 42 0.908
544
OLG003 Oligohydramnios 50 0.908
545
P AMY004 Amyloidosis 69 0.908
546
CYS001 Cystic Fibrosis 77 0.908
547
AMD002 Amed Syndrome, Digenic 36 0.908
548
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.908
549
RDN001 Reading Disorder 40 0.908
550
KRT002 Keratomalacia 54 0.908
551
NRN002 Neuronitis 31 0.908
552
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.908
553
CHR682 Chronic Bilirubin Encephalopathy 37 0.908
554
HYD001 Hydranencephaly 42 0.903
555
EXP004 Exophthalmos 50 0.903
556
AST006 Astigmatism 46 0.896
557
NVL002 Novelty Seeking Personality Trait 14 0.896
558
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.896
559
CHN002 Chancroid 36 0.896
560
FNT004 Fainting 29 0.896
561
HLX001 Helix Syndrome 47 0.883
562
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.883
563
P HYP750 Hypertriglyceridemia, Familial 61 0.883
564
CRB090 Cerebral Hypoxia 42 0.883
565
NRT004 Neuritis 53 0.882
566
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.878
567
RHB024 Rhabdomyosarcoma 2 65 0.875
568
WHT018 White Matter Hypoplasia-Corpus Callosum Agenesis-Intellectual Disability Syndrome 15 0.872
569
CYN002 Cyanosis, Transient Neonatal 43 0.870
570
P FRG001 Fragile X Syndrome 70 0.870
571
c ACT076 Acute Myocarditis 46 0.870
572
ILS001 Ileus 49 0.870
573
c FML191 Familial Long Qt Syndrome 54 0.870
574
PST092 Posttransplant Acute Limbic Encephalitis 29 0.870
575
P MXL015 Maxillary Sinusitis 37 0.856
576
HMP001 Hemopericardium 47 0.856
577
P GRV001 Graves' Disease 54 0.856
578
P PRC012 Pericardial Effusion 50 0.856
579
INT060 Intestinal Atresia 40 0.856
580
P INF032 Infertility 60 0.856
581
AMR003 Amaurosis Fugax 32 0.850
582
QDR002 Quadricuspid Aortic Valve 19 0.850
583
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.846
584
P CNR004 Cone-Rod Dystrophy 2 74 0.846
585
AMN001 Amenorrhea 53 0.843
586
P HYP040 Hypospadias 51 0.842
587
SPC030 Specific Language Disorder 25 0.842
588
MLT157 Multiple System Atrophy 1 69 0.827
589
ADJ001 Adjustment Disorder 46 0.827
590
MNN002 Mononeuritis Multiplex 38 0.826
591
P PRP019 Peripheral Nervous System Disease 57 0.826
592
PLM001 Pulmonary Tuberculosis 69 0.826
593
DMY004 Demyelinating Disease 50 0.826
594
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.826
595
c ATS007 Autism Spectrum Disorder 71 0.824
596
PRN038 Prune Belly Syndrome 55 0.810
597
P RNV001 Renovascular Hypertension 48 0.810
598
FCL014 Focal Epilepsy 53 0.810
599
IMM001 Immune-Complex Glomerulonephritis 36 0.810
600
PRP016 Paraplegia 52 0.810
601
CHR048 Chronic Rhinitis 46 0.810
602
P HYP083 Hypopituitarism 51 0.810
603
MNN021 Meningococcemia 34 0.810
604
P ALP008 Alopecia 53 0.810
605
MCR088 Microscopic Polyangiitis 51 0.810
606
P OVR082 Overgrowth Syndrome 41 0.810
607
CRB037 Cerebral Palsy 66 0.795
608
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.793
609
P END047 Endophthalmitis 53 0.793
610
P ANT001 Anterolateral Myocardial Infarction 34 0.793
611
P PLM036 Pulmonary Fibrosis 65 0.793
612
ART010 Arteriolosclerosis 37 0.793
613
APP008 Appendicitis 62 0.784
614
ALC003 Alcoholic Psychosis 27 0.782
615
CHD001 Chediak-Higashi Syndrome 66 0.774
616
STR089 Storage Pool Platelet Disease 46 0.774
617
HMP003 Hemopneumothorax 32 0.774
618
MTR002 Mitral Valve Insufficiency 51 0.774
619
P FRN011 Frontal Sinusitis 28 0.774
620
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.769
621
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.769
622
VSL002 Visual Epilepsy 39 0.769
623
ISL119 Isolated Optic Neuritis 27 0.769
624
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.763
625
ART109 Arterial Thoracic Outlet Syndrome 24 0.763
626
PHN003 Phenylketonuria 76 0.754
627
BRG013 Buerger Disease 56 0.753
628
PLY039 Polymorphic Reticulosis 16 0.753
629
ACT235 Acute Macular Neuroretinopathy 16 0.753
630
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.751
631
BCT022 Bacterial Infectious Disease 55 0.751
632
CVD001 Covid-19 59 0.748
633
c TYP008 Type 1 Diabetes Mellitus 77 0.729
634
NRN004 Neuroendocrine Tumor 55 0.729
635
ANT013 Anterior Spinal Artery Syndrome 31 0.729
636
EPG003 Epiglottitis 33 0.729
637
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 0.728
638
ATY001 Atypical Depressive Disorder 45 0.717
639
CHR066 Chronic Fatigue Syndrome 59 0.717
640
AZS001 Azoospermia 45 0.715
641
DST006 Diastolic Heart Failure 45 0.715
642
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.711
643
BNR002 Bone Resorption Disease 47 0.702
644
HMN048 Human Papillomavirus Infectious Disease 45 0.702
645
NRT011 Neurotrophic Keratopathy 36 0.702
646
INT075 Intracranial Hypertension 52 0.702
647
SYS071 Systemic Autoimmune Disease 35 0.702
648
ACT174 Acute Peripheral Arterial Occlusion 21 0.702
649
BSL004 Basilar Artery Occlusion 33 0.700
650
PNN001 Panniculitis 52 0.700
651
P MNN013 Meningitis 65 0.700
652
BRX001 Bruxism 50 0.696
653
PRT058 Pure Autonomic Failure 58 0.696
654
P ATS364 Autism 72 0.688
655
P PTN014 Patent Ductus Arteriosus 1 59 0.688
656
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.688
659
CMB007 Combined Immunodeficiency 56 0.688
660
TRC003 Trichomoniasis 53 0.688
661
NPH009 Nephrolithiasis 54 0.688
662
CRY004 Cryoglobulinemia 47 0.688
663
CHR073 Choreatic Disease 53 0.688
664
RHM001 Rheumatic Fever 59 0.688
665
CHL056 Cheilitis 46 0.688
666
ACT093 Actinic Cheilitis 38 0.688
667
FTT001 Fatty Liver Disease 61 0.688
668
NNT024 Neonatal Stroke 31 0.688
669
PNF002 Painful Legs and Moving Toes Syndrome 14 0.688
670
GST019 Gastrointestinal Stromal Tumor 78 0.685
671
CHC001 Chickenpox 56 0.680
672
P CRY007 Cryoglobulinemia, Familial Mixed 48 0.674
673
P LKM062 Leukemia, Acute Lymphoblastic 69 0.674
674
NRC003 Narcissistic Personality Disorder 25 0.674
675
ANS004 Anisometropia 31 0.674
676
SYS003 Systolic Heart Failure 49 0.674
677
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.674
678
CNT060 Central Serous Chorioretinopathy 38 0.674
679
SPS057 Spasticity 43 0.674
680
PRM329 Premature Aging 36 0.674
681
P CRN300 Coronary Heart Disease 1 73 0.670
682
P ANG015 Angioedema 56 0.663
683
PNT023 Pontine Hemorrhage 17 0.663
684
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.658
685
ECT026 Ectopic Pregnancy 47 0.658
686
P INF037 Inflammatory Bowel Disease 53 0.658
687
CRN045 Corneal Dystrophy and Perceptive Deafness 44 0.658
688
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.658
689
LYM133 Lymphoma, Hodgkin, Classic 69 0.658
690
c HYD064 Hydrocephalus, Congenital, 1 51 0.658
691
c CRN279 Cornea Plana 1, Autosomal Dominant 19 0.658
692
DRV001 Dravet Syndrome 69 0.658
693
c MCR312 Microphthalmia, Syndromic 10 39 0.658
694
P WSK001 Wiskott-Aldrich Syndrome 72 0.658
695
c MCR115 Microvascular Complications of Diabetes 5 65 0.658
696
c MYC058 Myocardial Infarction 2 23 0.658
697
FRY006 Fryns Microphthalmia Syndrome 52 0.658
698
MSC190 Muscular Disease 36 0.658
699
KRT008 Keratopathy 46 0.658
700
LYM027 Lymphopenia 56 0.658
701
P HYP061 Hypertrophic Cardiomyopathy 68 0.658
702
RTN003 Retinal Ischemia 48 0.658
703
CRY003 Cryptosporidiosis 55 0.658
704
GNT046 Genetic Epilepsy with Febrile Seizures Plus 30 0.658
705
DRG017 Drug-Induced Vasculitis 16 0.658
706
c BCT013 Bacterial Pneumonia 47 0.658
707
PRM003 Premature Ejaculation 44 0.643
708
P THR015 Thrombophilia 51 0.643
709
P ATR010 Atrial Heart Septal Defect 58 0.643
710
P RTN024 Retinoblastoma 72 0.642
711
RST023 Resting Heart Rate, Variation in 40 0.642
712
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.642
713
c THY107 Thymoma, Familial 42 0.642
714
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 54 0.642
715
P LNG064 Lung Cancer Susceptibility 3 69 0.642
716
c ERL056 Early-Onset Parkinson's Disease 39 0.642
717
P VNT002 Ventricular Septal Defect 58 0.642
718
P DDN001 Duodenal Ulcer 52 0.642
719
HYP060 Hyperinsulinism 53 0.642
720
P THY023 Thymoma 64 0.642
721
BLR008 Bilirubin Metabolic Disorder 57 0.642
722
P CND004 Candidiasis 57 0.642
723
CRT012 Cortical Blindness 42 0.642
724
HRT012 Heart Valve Disease 53 0.642
725
GTR002 Goiter 52 0.642
726
MCR013 Microphthalmia 59 0.642
727
MCR018 Microcytic Anemia 46 0.642
728
CRV002 Cervix Uteri Carcinoma in Situ 48 0.642
729
P TXP001 Toxoplasmosis 59 0.642
730
CRV045 Cervical Intraepithelial Neoplasia 38 0.642
731
SPC003 Specific Developmental Disorder 32 0.628
732
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.628
733
BRN045 Brunner Syndrome 52 0.628
734
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.628
735
BLP051 Blepharophimosis-Impaired Intellectual Development Syndrome 21 0.628
736
P SHW006 Shwachman-Diamond Syndrome 1 65 0.628
737
CYC008 Cyclic Vomiting Syndrome 46 0.628
738
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.628
739
P VND007 Van Der Woude Syndrome 1 60 0.628
740
OVL001 Ovalocytosis, Southeast Asian 34 0.628
741
P MGR003 Migraine with Aura 51 0.628
742
BRB002 Barbiturate Dependence 27 0.628
743
DRG001 Drug Psychosis 30 0.628
744
DPM001 Dopamine Beta-Hydroxylase Deficiency 54 0.628
745
SPN012 Spindle Cell Hemangioma 31 0.628
746
PRL010 Prolactin Producing Pituitary Tumor 33 0.628
747
INH002 Inhibited Male Orgasm 27 0.628
748
ALC013 Alcohol-Induced Mental Disorder 19 0.628
749
P STR001 Striatonigral Degeneration 37 0.628
750
DRG004 Drug-Induced Mental Disorder 22 0.628
751
VRL011 Viral Infectious Disease 60 0.628
752
P OST009 Osteochondritis Dissecans 61 0.628
753
CYT018 Cytochrome P450 2d6 Variant 26 0.628
754
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.628
755
c ERL020 Early-Onset Schizophrenia 43 0.628
756
FML169 Familial Osteochondritis Dissecans 29 0.628
757
LNG095 Lung Abscess 50 0.624
758
P OMP004 Omphalocele 47 0.624
759
ALV005 Alveolar Soft Part Sarcoma 61 0.624
760
FBR054 Fibroma 44 0.624
761
ERY003 Erythema Multiforme 56 0.624
762
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 36 0.624
763
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.624
764
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.624
765
SCH018 Schizencephaly 52 0.624
766
P LSS002 Lissencephaly 52 0.624
767
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 37 0.624
768
c GRV008 Graves Disease 1 54 0.624
769
c LSS005 Lissencephaly 1 57 0.624
770
SVR097 Severe Cutaneous Adverse Reaction 68 0.624
771
VCC001 Vaccinia 49 0.624
772
P SCK002 Sick Sinus Syndrome 55 0.624
773
CHL068 Cholestasis 61 0.624
774
P RTN022 Retinal Vein Occlusion 54 0.624
775
GLC106 Glucocorticoid Resistance, Generalized 47 0.624
776
P PLY011 Polycystic Ovary Syndrome 57 0.624
777
P PLY019 Polyneuropathy 52 0.624
778
P RHB003 Rhabdomyosarcoma 66 0.624
779
INT078 Intracranial Thrombosis 50 0.624
780
IRT001 Iritis 45 0.624
781
P OSS001 Ossifying Fibroma 42 0.624
782
EXT034 Extrinsic Allergic Alveolitis 56 0.624
783
ACT060 Acute Vascular Insufficiency of Intestine 29 0.624
784
P DBT005 Diabetes Insipidus 54 0.624
785
c BCT007 Bacterial Meningitis 55 0.624
786
HYP074 Hypersensitivity Vasculitis 53 0.624
787
CHR178 Chromosomal Triplication 33 0.624
788
INF043 Infantile Apnea 21 0.624
789
SNG003 Single Ventricular Heart 30 0.624
790
ERY066 Erythema Multiforme Major 29 0.624
791
IDP031 Idiopathic Hypersomnia 39 0.624
792
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.624
793
PRP015 Paraphilia Disorder 33 0.622
794
ADP007 Adie Pupil 40 0.622
795
APR001 Apraxia 51 0.605
796
ALL003 Allergic Rhinitis 66 0.605
797
SNT005 Sinoatrial Node Disease 48 0.605
798
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.605
799
MSC157 Muscular Dystrophy, Duchenne Type 78 0.605
800
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.605
801
P RST001 Restless Legs Syndrome 52 0.605
802
TRC010 Trichotillomania 51 0.605
803
WST001 West Syndrome 64 0.605
804
c HMC039 Hemochromatosis, Type 1 73 0.605
805
c GLL024 Gallbladder Disease 1 53 0.605
806
CHR669 Chromosome 2p16.3 Deletion Syndrome 22 0.605
807
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.605
808
PRN035 Perniosis 27 0.605
809
NRL005 Neurilemmoma 60 0.605
810
WRN003 Wernicke Encephalopathy 45 0.605
811
P BRB001 Beriberi 44 0.605
812
KRT009 Keratosis 52 0.605
813
LPT001 Leptospirosis 65 0.605
814
MMB001 Membranoproliferative Glomerulonephritis 56 0.605
815
P ART023 Arthropathy 59 0.605
816
c CHR038 Chronic Maxillary Sinusitis 32 0.605
817
LCK001 Locked-in Syndrome 44 0.605
818
P HML001 Hemolytic-Uremic Syndrome 52 0.605
819
HPT004 Hepatic Coma 43 0.605
820
LTN001 Latent Syphilis 34 0.605
821
TRT003 Tertiary Syphilis 36 0.605
822
P BLL007 Bullous Skin Disease 35 0.605
823
HMP009 Haemophilus Influenzae 41 0.605
824
FCL090 Facial Cleft 32 0.605
825
IMM206 Immune Complex Mediated Vasculitis 13 0.605
826
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.605
827
P MYM013 Moyamoya Disease 1 59 0.598
828
HMS001 Hemosiderosis 48 0.598
829
LYM017 Lyme Disease 63 0.598
830
P APL001 Aplastic Anemia 72 0.584
831
CLS016 Clostridium Difficile Colitis 49 0.584
832
RTN017 Retinal Detachment 60 0.584
833
c SCH079 Schizophrenia 1 44 0.584
834
GNT050 Genitourinary Tract Anomalies 28 0.584
835
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.584
837
P KLZ004 Kala-Azar 1 41 0.584
838
PLL012 Pollen Allergy 44 0.584
839
P CRN037 Craniosynostosis 67 0.584
840
P ESS003 Essential Thrombocythemia 68 0.584
841
CNT046 Central Nervous System Vasculitis 45 0.584
842
FCL012 Facial Paralysis 49 0.584
843
IRR001 Irregular Astigmatism 32 0.584
844
CNT016 Central Retinal Vein Occlusion 53 0.584
845
HST001 Histrionic Personality Disorder 27 0.584
846
c PRM022 Primary Syphilis 32 0.584
847
SYN005 Synostosis 43 0.584
848
DPN001 Dependent Personality Disorder 26 0.584
849
HST011 Histoplasmosis 54 0.584
850
ALC010 Alcoholic Cardiomyopathy 42 0.584
851
P END046 Endometritis 46 0.584
852
PTT002 Potter's Syndrome 39 0.584
853
CNT015 Central Sleep Apnea 46 0.584
854
ACQ011 Acquired Agranulocytosis 10 0.584
855
SCT002 Scotoma 42 0.584
856
LSH001 Leishmaniasis 63 0.584
857
CWP001 Cowpox 44 0.584
858
PLY012 Polyhydramnios 46 0.584
859
HRS011 Horseshoe Kidney 31 0.584
860
RTR011 Retroperitoneal Fibrosis 47 0.584
861
MST020 Mast Cell Activation Syndrome 27 0.584
862
MLT084 Multicystic Dysplastic Kidney 42 0.584
863
UNL014 Unilateral Multicystic Dysplastic Kidney 19 0.584
864
WLF001 Wolff-Parkinson-White Syndrome 63 0.574
865
P TMP001 Temporal Lobe Epilepsy 49 0.570
866
RTR001 Retrograde Amnesia 41 0.570
867
BNN003 Bone Inflammation Disease 47 0.570
868
P PRN026 Porencephaly 54 0.560
869
PPL052 Papillomatosis, Confluent and Reticulated 34 0.560
870
TRP006 Tarp Syndrome 58 0.560
871
c LKM061 Leukemia, Acute Myeloid 83 0.560
872
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.560
873
c PCH010 Pachyonychia Congenita 3 43 0.560
874
RFL001 Reflex Sympathetic Dystrophy 51 0.560
875
HLC007 Helicobacter Pylori Infection 67 0.560
876
STR077 Streptococcal Toxic-Shock Syndrome 34 0.560
877
HYP080 Hypogonadism 49 0.560
878
KDN001 Kidney Cortex Necrosis 31 0.560
879
CRT016 Carotid Artery Disease 52 0.560
880
RTN021 Retinal Vascular Occlusion 45 0.560
881
ANT019 Anterograde Amnesia 38 0.560
882
P PRP029 Porphyria 60 0.560
883
SPN035 Spindle Cell Sarcoma 51 0.560
884
CPN001 C-P Angle Neurinoma 8 0.560
885
P PRL003 Proliferative Glomerulonephritis 43 0.560
886
PRM024 Primary Angle-Closure Glaucoma 38 0.560
887
SRC014 Sarcoma 64 0.560
888
RLP003 Relapsing Fever 50 0.560
890
ALL014 Allergic Encephalomyelitis 34 0.560
891
c CNG216 Congenital Hydrocephalus 50 0.560
892
ALL012 Allergic Angiitis 24 0.560
893
SDD008 Sudden Sensorineural Hearing Loss 41 0.560
894
SRN002 Sirenomelia 28 0.560
895
SPS019 Spastic Paraparesis 38 0.560
896
PRS063 Paresthesia 39 0.560
897
APN008 Apnea, Obstructive Sleep 66 0.557
898
P SCL018 Scoliosis 57 0.533
899
DMN031 Dementia, Lewy Body 65 0.533
900
P NSP012 Nasopharyngeal Carcinoma 60 0.533
901
c DPH024 Diaphragmatic Hernia, Congenital 63 0.533
902
HMR039 Hemorrhage, Intracerebral 57 0.533
903
P GRN010 Granular Cell Tumor 40 0.533
904
PRS036 Parasitic Protozoa Infectious Disease 44 0.533
905
AKN002 Akinetic Mutism 36 0.533
906
SMT001 Somatization Disorder 49 0.533
907
P ADN016 Adenocarcinoma 63 0.533
908
EXS001 Exostosis 49 0.533
909
ERD001 Erdheim-Chester Disease 53 0.533
910
ADR005 Adrenal Carcinoma 58 0.533
911
KLP001 Kleptomania 36 0.533
912
HYP016 Hypochondriasis 47 0.533
913
SLP001 Sleeping Sickness 56 0.533
914
RMS001 Rem Sleep Behavior Disorder 47 0.533
915
HLL005 Hallucinogen Dependence 23 0.533
916
IRR002 Irritable Bowel Syndrome 64 0.533
917
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.532
918
CRP032 Corpus Callosum, Agenesis of 49 0.532
919
ANK020 Ankyloglossia with or Without Tooth Anomalies 45 0.532
920
HMR015 Humeroradial Synostosis 36 0.532
921
OBS082 Obstructive Nephropathy 41 0.532
922
P SLM003 Salmonellosis 54 0.532
923
LTH001 Lethal Midline Granuloma 31 0.532
924
ASY002 Asymptomatic Neurosyphilis 41 0.532
925
PNC001 Pancytopenia 52 0.532
926
LYM011 Lymphogranuloma Venereum 32 0.532
927
PRT011 Protein C Deficiency 47 0.532
928
PPL021 Papilledema 49 0.532
929
P OVR049 Ovarian Disease 50 0.532
930
IGG001 Iga Glomerulonephritis 50 0.532
931
INS001 Insulinoma 59 0.532
932
P GST044 Gastritis 55 0.532
933
NPH010 Nephrosclerosis 50 0.532
934
P URT039 Urticaria 57 0.532
935
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.532
936
ADN001 Adenosine Deaminase Deficiency 59 0.532
937
P OVR046 Ovarian Cyst 43 0.532
938
MSC020 Mosaic Trisomy 8 35 0.532
939
NRS003 Neurosyphilis 45 0.532
940
THN005 Thunderclap Headache 16 0.532
941
PCH002 Pachygyria 31 0.532
942
MLR002 Miliary Tuberculosis 47 0.532
943
AML065 Amelia 29 0.532
944
DWN001 Down Syndrome 70 0.529
945
GST045 Gastroenteritis 58 0.529
946
CRH001 Crohn's Disease 80 0.529
947
PLY150 Polykaryocytosis Inducer 29 0.495
948
SHR107 Short Stature-Obesity Syndrome 25 0.495
949
MTC212 Mitchell Syndrome 26 0.495
950
HYP748 Hypertelorism 46 0.495
951
P PRP034 Purpura Fulminans 41 0.495
952
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.495
953
CYC001 Cycloplegia 35 0.495
954
TRC005 Tracheal Stenosis 43 0.495
955
P ESP024 Esophagitis 60 0.495
956
PRT014 Protein S Deficiency 46 0.495
957
LTR003 Lateral Medullary Syndrome 35 0.495
958
CHR093 Chronic Orbital Inflammation 22 0.495
959
ACT038 Acute Retrobulbar Neuritis 25 0.495
960
MCC002 Mucocutaneous Leishmaniasis 47 0.495
961
KLD004 Keloid Disorder 38 0.495
962
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.495
963
CHR067 Chronic Intestinal Vascular Insufficiency 34 0.495