Search results for antipsychotics

1399 hits were found for antipsychotics

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 74 41.035
2
P BPL003 Bipolar Disorder 56 22.409
3
c MJR022 Major Affective Disorder 8 37 21.596
4
c MJR024 Major Affective Disorder 9 40 21.596
5
PSY004 Psychotic Disorder 66 21.292
6
TRD006 Tardive Dyskinesia 53 16.836
7
SCH012 Schizoaffective Disorder 49 16.509
8
P DMN002 Dementia 65 12.690
9
HYP020 Hyperprolactinemia 63 11.724
10
P PRK039 Parkinsonism 55 10.798
11
SCH003 Schizophreniform Disorder 54 10.733
12
MNT002 Mental Depression 56 10.477
13
LPD008 Lipid Metabolism Disorder 61 10.365
14
SBC016 Subacute Delirium 42 10.351
15
DPR016 Depression 64 10.179
16
P MJR001 Major Depressive Disorder 68 9.735
17
NRL004 Neuroleptic Malignant Syndrome 52 9.577
18
P MVM001 Movement Disease 61 9.492
19
DSS008 Disease of Mental Health 74 9.307
20
MDD011 Mood Disorder 61 9.014
21
P DYS154 Dystonia 64 8.026
22
SXL003 Sexual Disorder 49 7.996
23
P MJR007 Major Affective Disorder 1 42 7.640
24
P SBS003 Substance Abuse 54 7.118
25
P ATT013 Attention Deficit-Hyperactivity Disorder 65 7.092
26
P PRS038 Personality Disorder 65 6.647
27
c ATS007 Autism Spectrum Disorder 71 6.567
28
GRN017 Granulocytopenia 42 6.540
29
c BPL002 Bipolar I Disorder 47 6.491
30
HYP066 Hyperglycemia 60 6.481
31
OBS002 Obsessive-Compulsive Disorder 67 6.413
32
P TRM003 Tremor 50 6.165
33
c TYP009 Type 2 Diabetes Mellitus 91 6.027
34
CRD132 Cardiac Conduction Defect 59 5.780
35
P ATS364 Autism 72 5.780
36
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 5.628
37
P ALZ034 Alzheimer Disease 87 5.578
38
PST028 Post-Traumatic Stress Disorder 58 5.336
39
END040 Endogenous Depression 54 5.273
40
c THR092 Thrombophilia Due to Thrombin Defect 74 5.249
41
PRN009 Paranoid Schizophrenia 49 5.143
42
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 4.963
43
c MJR006 Major Affective Disorder 5 32 4.716
44
c MJR003 Major Affective Disorder 6 32 4.716
45
DLS001 Delusional Disorder 44 4.648
46
P TCD001 Tic Disorder 50 4.630
47
GLC003 Glucose Intolerance 53 4.555
48
ETN001 Eating Disorder 59 4.535
49
P PRV006 Pervasive Developmental Disorder 52 4.534
50
P PRK057 Parkinson Disease, Late-Onset 79 4.508
51
P HYP750 Hypertriglyceridemia, Familial 61 4.424
52
ANX010 Anxiety 70 4.423
53
ACT084 Acute Stress Disorder 53 4.405
54
c ERL020 Early-Onset Schizophrenia 43 4.360
55
DBT084 Diabetes Mellitus, Ketosis-Prone 59 4.355
56
P DBT009 Diabetes Mellitus 67 4.251
57
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.241
58
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.241
59
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.241
60
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.241
61
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.241
62
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.241
63
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 4.241
64
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.241
65
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.241
66
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 4.230
67
PRT058 Pure Autonomic Failure 58 4.128
68
CNS004 Constipation 56 4.080
69
NRT001 Neurotic Disorder 56 4.074
70
CND002 Conduct Disorder 50 4.044
71
c MJR008 Major Affective Disorder 2 34 4.024
72
c MJR023 Major Affective Disorder 7 33 4.024
73
c MJR004 Major Affective Disorder 4 28 4.024
74
IMP005 Impotence 52 3.959
75
HYP080 Hypogonadism 49 3.946
76
AMN001 Amenorrhea 53 3.945
77
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.825
78
P NTR004 Neutropenia 62 3.817
79
GLC096 Galactorrhea 40 3.777
81
CRB039 Cerebrovascular Disease 65 3.735
82
GLL008 Gilles De La Tourette Syndrome 64 3.689
83
OCL069 Ocular Motor Apraxia 57 3.657
84
ANR007 Anorexia Nervosa 59 3.600
85
LRN003 Learning Disability 49 3.581
86
P PNM007 Pneumonia 64 3.580
87
c HYP836 Hypercholesterolemia, Familial, 1 73 3.526
88
AVD001 Avoidant Personality Disorder 49 3.494
89
PLM033 Pulmonary Embolism 58 3.412
90
BRD004 Borderline Personality Disorder 53 3.400
91
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.282
92
STR067 Stroke, Ischemic 79 3.238
93
P MYC008 Myocarditis 59 3.215
94
GST033 Gestational Diabetes 60 3.162
95
P SLP005 Sleep Disorder 61 3.108
96
P ALC033 Alcohol Use Disorder 67 3.070
97
PRP007 Priapism 46 3.015
98
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 2.998
99
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 2.998
100
AGN016 Aging 53 2.987
101
LNG015 Lingual-Facial-Buccal Dyskinesia 47 2.983
102
INF021 Infant Gynecomastia 30 2.938
103
GYN001 Gynecomastia 48 2.938
104
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 2.926
105
47X002 47,xyy 47 2.872
106
GNR004 Generalized Anxiety Disorder 54 2.803
107
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 2.794
108
P MYC007 Myocardial Infarction 69 2.780
109
SYN036 Syncope 44 2.762
110
ALC007 Alcohol Dependence 65 2.752
111
P HNT016 Huntington Disease 73 2.745
112
VSC002 Vascular Dementia 59 2.707
113
DYS073 Dysphagia 53 2.666
114
P CRN300 Coronary Heart Disease 1 73 2.652
115
GLB002 Glioblastoma 67 2.614
116
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.588
117
P OST002 Osteoporosis 76 2.588
118
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.588
119
HND015 Hand Skill, Relative 29 2.577
120
P SZR006 Seizure Disorder 69 2.554
121
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 2.530
122
HYP060 Hyperinsulinism 53 2.522
123
PHY002 Physical Disorder 40 2.426
124
CYT002 Cytokine Deficiency 43 2.425
125
AND005 Androgen Insensitivity Syndrome, Mild 21 2.422
126
TBC004 Tobacco Addiction 63 2.397
127
c SCH085 Schizophrenia 2 27 2.369
128
TRM010 Traumatic Brain Injury 50 2.361
129
P PNC025 Panic Disorder 52 2.355
130
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 2.355
131
P RST001 Restless Legs Syndrome 52 2.319
132
P NRB001 Neuroblastoma 66 2.296
133
OPP004 Oppositional Defiant Disorder 48 2.293
134
BRN071 Brain Injury 50 2.293
135
P CRD119 Cardiac Arrest 68 2.244
136
c SCH079 Schizophrenia 1 44 2.238
137
P LNG028 Long Qt Syndrome 63 2.224
138
FBR047 Fibromyalgia 57 2.203
139
EPT021 Epithelial Recurrent Erosion Dystrophy 45 2.203
140
RCK004 Rickets 64 2.197
141
P CTR002 Cataract 59 2.189
142
P PNC044 Pancreatitis 61 2.148
143
P RSP003 Respiratory Failure 73 2.141
144
OCL066 Oculogyric Crisis 35 2.125
145
CVD001 Covid-19 59 2.114
146
48X005 48,xyyy 39 2.113
147
SCH011 Schizotypal Personality Disorder 36 2.082
148
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 2.068
149
CHR073 Choreatic Disease 53 2.068
150
CRD223 Cardiac Arrhythmia 63 2.067
151
HYP056 Hypoglycemia 65 2.064
152
P URN019 Urinary Tract Infection 48 2.057
153
CHL078 Childhood-Onset Schizophrenia 29 2.054
154
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.038
155
HYP005 Hypokalemia 55 2.019
156
THR024 Thrombosis 56 1.997
157
P EPL164 Epilepsy 70 1.993
158
ALL029 Allergic Disease 61 1.990
159
ANT039 Antisynthetase Syndrome 55 1.990
160
SRT004 Serotonin Syndrome 54 1.984
161
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.970
162
P CHR345 Chronic Pain 50 1.958
163
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.952
164
ADL002 Adult Syndrome 69 1.949
165
ASP007 Aspiration Pneumonia 49 1.931
166
P MYC033 Myoclonus 46 1.910
167
ATN005 Autonomic Dysfunction 45 1.896
168
ILS001 Ileus 49 1.891
169
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.869
170
DYS009 Dysthymic Disorder 51 1.864
171
SVR004 Severe Combined Immunodeficiency 70 1.849
172
c ACT027 Acute Pancreatitis 60 1.843
173
P HYP098 Hypereosinophilic Syndrome 66 1.842
174
P HYP086 Hypothyroidism 68 1.821
175
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.820
176
FTT001 Fatty Liver Disease 61 1.802
177
RHB024 Rhabdomyosarcoma 2 65 1.782
178
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.776
179
c ACT071 Acute Kidney Failure 60 1.756
180
c BLD140 Blood Group, I System 47 1.742
181
P BRS047 Breast Cancer 97 1.717
182
PTT037 Pituitary Tumors 44 1.715
183
GLL048 Glial Tumor 51 1.709
184
DGR001 Digeorge Syndrome 62 1.708
185
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.694
186
GLM045 Glioma 62 1.693
187
P ENC004 Encephalitis 61 1.687
188
P SLP006 Sleep Apnea 69 1.680
189
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.666
190
CHR158 Charles Bonnet Syndrome 23 1.660
191
DMN031 Dementia, Lewy Body 65 1.649
192
c ACT068 Acute Cystitis 60 1.635
193
c SCH081 Schizophrenia 6 27 1.620
194
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.619
195
MLD018 Mild Cognitive Impairment 48 1.604
196
HMC014 Homocysteinemia 52 1.604
197
SVR001 Severe Acute Respiratory Syndrome 68 1.604
198
BDY001 Body Dysmorphic Disorder 40 1.587
199
SMT001 Somatization Disorder 49 1.575
200
CNN002 Cannabis Abuse 44 1.569
201
CNG034 Congestive Heart Failure 69 1.568
202
WTH001 Withdrawal Disorder 47 1.565
203
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.546
204
CCN001 Cocaine Dependence 47 1.531
205
P KHL003 Kohlschutter-Tonz Syndrome 57 1.526
206
CHL079 Children's Interstitial Lung Disease 25 1.526
207
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 1.514
208
END057 Endometrial Cancer 76 1.499
209
ADN018 Adenoma 58 1.464
210
FRN006 Frontotemporal Dementia 68 1.459
211
P HDC001 Headache 56 1.454
212
SCL003 Social Phobia 48 1.435
213
PST103 Postpartum Psychosis 31 1.435
214
P LVR013 Liver Disease 68 1.416
215
DRG016 Drug Induced Dyskinesia 23 1.394
216
P PHC003 Pheochromocytoma 70 1.392
217
ADR040 Adrenal Gland Pheochromocytoma 45 1.392
218
TRC010 Trichotillomania 51 1.389
219
SBS004 Substance Dependence 46 1.383
220
AMN003 Amnestic Disorder 53 1.376
221
ISC004 Ischemia 61 1.375
222
c ACT075 Acute Myocardial Infarction 55 1.375
223
c CHR056 Chronic Tic Disorder 36 1.373
224
TXC005 Toxic Shock Syndrome 61 1.366
225
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 1.362
226
P HPT021 Hepatitis 68 1.359
227
INS024 Insulin-Like Growth Factor I 77 1.357
228
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.357
229
PRL008 Paralytic Ileus 44 1.357
230
P FML340 Familial Episodic Pain Syndrome 50 1.348
231
SPS134 Spasmodic Dystonia 28 1.339
232
SPS016 Spasmodic Dysphonia 32 1.339
233
c FML191 Familial Long Qt Syndrome 54 1.326
234
ANG054 Angina Pectoris 65 1.322
235
INP001 Inappropriate Adh Syndrome 48 1.319
236
P VSC007 Vascular Disease 62 1.318
237
HYP016 Hypochondriasis 47 1.310
238
c SCH051 Schizophrenia 4 35 1.303
239
HYP264 Hypertonia 35 1.295
240
RST023 Resting Heart Rate, Variation in 40 1.289
241
SBS005 Substance-Induced Psychosis 31 1.287
242
BLM002 Bulimia Nervosa 56 1.284
243
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 1.282
244
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.267
245
HLX001 Helix Syndrome 47 1.255
246
P PTT006 Pituitary Adenoma 55 1.255
247
BNR002 Bone Resorption Disease 47 1.253
248
P MLG056 Malignant Hyperthermia 65 1.253
249
SWL001 Swallowing Disorders 37 1.253
250
ADJ001 Adjustment Disorder 46 1.252
251
P HRT032 Heart Disease 84 1.244
252
CCN002 Cocaine Abuse 49 1.244
253
PPT005 Peptic Ulcer Disease 58 1.226
254
P EXN002 Exanthem 58 1.218
255
P HYP265 Hypotonia 42 1.218
256
P BRG001 Brugada Syndrome 69 1.217
257
PRS063 Paresthesia 39 1.217
258
LWF001 Low-Flow Priapism 16 1.208
259
P GLM040 Glioma Susceptibility 1 70 1.198
260
MLN003 Melancholia 41 1.189
261
P TRT019 Torticollis 47 1.188
262
P TRN020 Turner Syndrome 67 1.185
263
P LCT001 Lactic Acidosis 50 1.184
264
DWN001 Down Syndrome 70 1.179
265
P ATR011 Atrial Fibrillation 66 1.178
266
P PTS002 Ptosis 52 1.178
267
DSS032 Disease by Infectious Agent 55 1.178
268
DBT010 Diabetic Neuropathy 54 1.166
269
P BCL017 B-Cell Lymphoma 57 1.156
270
ANT011 Antisocial Personality Disorder 47 1.151
271
ATR057 Atrioventricular Block 54 1.145
272
CLT003 Colitis 63 1.134
273
c HYP595 Hypertension, Essential 84 1.134
274
CYT018 Cytochrome P450 2d6 Variant 26 1.134
275
P APL001 Aplastic Anemia 72 1.134
276
P RTN008 Retinitis Pigmentosa 79 1.134
277
DNT012 Dental Caries 53 1.134
278
NRR001 Neuroretinitis 42 1.134
279
RTN023 Retinitis 45 1.134
280
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.127
281
HDN002 Head Injury 44 1.126
282
P GST053 Gastric Cancer 82 1.122
284
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.118
285
P URT039 Urticaria 57 1.118
286
HMN044 Human Immunodeficiency Virus Type 1 76 1.115
287
TXC002 Toxic Encephalopathy 51 1.115
288
BRX001 Bruxism 50 1.110
289
PRT037 Pertussis 49 1.110
290
ALL014 Allergic Encephalomyelitis 34 1.110
291
IRR002 Irritable Bowel Syndrome 64 1.109
292
INT007 Intermediate Coronary Syndrome 53 1.100
293
FML035 Familial Hyperlipidemia 54 1.094
294
STT001 Status Epilepticus 58 1.082
295
P HYP263 Hypersomnia 40 1.082
296
P ACN011 Acne 55 1.073
297
P KDN018 Kidney Disease 71 1.073
298
STT041 Stuttering 52 1.064
299
BCT022 Bacterial Infectious Disease 55 1.055
300
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.054
301
P MLT020 Multiple Sclerosis 79 1.044
302
CLF027 Cleft Palate, Isolated 64 1.044
303
P FNG006 Feingold Syndrome 1 61 1.042
304
c SCH080 Schizophrenia 3 27 1.023
305
IMP006 Impulse Control Disorder 44 1.023
306
P MYG005 Myoglobinuria 40 1.012
307
P INT070 Intestinal Obstruction 57 1.012
308
P HRP006 Herpes Simplex 65 1.012
309
IMM167 Immune Deficiency Disease 76 1.001
310
END086 End Stage Renal Disease 54 1.001
311
P CRB088 Cerebral Atrophy 32 1.001
312
P HYP076 Hyperthyroidism 53 1.001
313
c CHR684 Chronic Kidney Disease 73 0.990
314
NNL006 Non-Alcoholic Steatohepatitis 54 0.986
315
AGR002 Agoraphobia 45 0.979
316
c SCH045 Schizophrenia 12 23 0.978
317
INT025 Intermittent Explosive Disorder 39 0.978
318
PST011 Pustulosis of Palm and Sole 52 0.978
319
P ADL010 Adult Respiratory Distress Syndrome 70 0.978
320
TTN003 Tetanus 64 0.978
321
P PSR002 Psoriasis 63 0.978
322
c MGR028 Migraine with or Without Aura 1 63 0.971
323
P ENC018 Encephalopathy 62 0.971
324
PLC008 Placenta Disease 48 0.966
325
DRG003 Drug Dependence 46 0.963
326
P BLP003 Blepharospasm 45 0.955
327
P RHN004 Rhinitis 56 0.947
328
PSD088 Pseudobulbar Affect 33 0.947
329
ACT088 Acute Insulin Response 39 0.940
330
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.926
331
ATH013 Atherosclerosis Susceptibility 63 0.926
332
P PLY011 Polycystic Ovary Syndrome 57 0.921
333
P ANR048 Aniridia 1 66 0.920
334
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.920
335
CHR682 Chronic Bilirubin Encephalopathy 37 0.920
336
BNB002 Bainbridge-Ropers Syndrome 45 0.911
337
P HYD006 Hydrocephalus 62 0.911
338
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.896
339
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.896
340
TRN015 Transient Cerebral Ischemia 62 0.895
341
P MYP004 Myopathy 67 0.895
342
KRT001 Keratoconjunctivitis Sicca 49 0.895
343
MTN003 Motion Sickness 50 0.885
344
P BND020 Bone Disease 60 0.885
345
XRP001 Xerophthalmia 42 0.885
346
P THR014 Thrombocytopenia 66 0.885
347
c MTC054 Mitochondrial Dna Depletion Syndrome 7 53 0.884
348
P CLR023 Colorectal Cancer 100 0.879
349
c SCH087 Schizophrenia 18 28 0.879
350
P HPT023 Hepatocellular Carcinoma 95 0.879
351
INT075 Intracranial Hypertension 52 0.879
352
c SCH082 Schizophrenia 5 23 0.876
353
P ANG015 Angioedema 56 0.876
354
CHL068 Cholestasis 61 0.866
355
ADG002 Audiogenic Seizures 25 0.862
356
c ATR087 Atrial Standstill 1 74 0.856
357
PRS045 Prostatic Hypertrophy 53 0.856
358
PST021 Postpartum Depression 50 0.853
359
ANV001 Anovulation 46 0.846
360
SKN016 Skin Disease 63 0.846
361
GST023 Gastric Ulcer 52 0.842
362
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.842
363
c ACT134 Acute Liver Failure 57 0.842
364
PNG002 Pain Agnosia 51 0.835
365
c HPT003 Hepatitis a 63 0.831
366
ENT011 Enterocolitis 55 0.821
367
P BNC003 Bone Cancer 58 0.821
368
ORM002 Oromandibular Dystonia 41 0.814
369
P SYP003 Syphilis 59 0.814
370
P GRV001 Graves' Disease 54 0.814
371
PRC013 Pericarditis 53 0.814
372
P PRD006 Prader-Willi Syndrome 60 0.802
373
P MYS003 Myasthenia Gravis 67 0.797
374
P HYP111 Hyperprolinemia 44 0.797
375
ORL011 Oral Cancer 60 0.797
376
NTR005 Nutritional Deficiency Disease 60 0.797
377
KRT002 Keratomalacia 54 0.797
378
ATX019 Ataxia with Vitamin E Deficiency 44 0.797
379
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.797
380
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.797
381
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.797
382
c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 44 0.794
383
BRB002 Barbiturate Dependence 27 0.794
384
DPH028 Diaphragmatic Flutter 12 0.794
385
FNT004 Fainting 29 0.794
386
WLS001 Wilson Disease 70 0.790
387
c TYP008 Type 1 Diabetes Mellitus 77 0.790
388
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.790
389
ISC015 Ischemic Colitis 43 0.778
390
c SCH064 Schizophrenia 10 27 0.778
391
c SYS001 Systemic Lupus Erythematosus 85 0.778
392
ASY002 Asymptomatic Neurosyphilis 41 0.778
393
P LPS004 Lupus Erythematosus 61 0.778
394
NRS003 Neurosyphilis 45 0.778
395
OPD006 Opioid Addiction 48 0.778
396
PRN019 Perinatal Necrotizing Enterocolitis 60 0.768
397
DSR019 Disorder of Proline Metabolism 5 0.768
398
MYX004 Myxedema 43 0.765
399
c BRN108 Branchiootic Syndrome 1 63 0.765
400
PRP027 Peripheral Vascular Disease 71 0.765
401
c SCH053 Schizophrenia 13 27 0.765
402
FCL022 Focal Dystonia 41 0.765
403
c DLT002 Dilated Cardiomyopathy 79 0.765
404
CHL014 Cholera 62 0.765
405
CRB004 Cerebral Artery Occlusion 45 0.765
406
CHR066 Chronic Fatigue Syndrome 59 0.765
407
P THY032 Thyroiditis 56 0.765
408
P MYC084 Mycobacterium Tuberculosis 1 68 0.752
409
P ART021 Arteriosclerosis 53 0.752
410
BRN014 Bronchopneumonia 52 0.752
411
P OVR049 Ovarian Disease 50 0.752
412
LWC001 Low Compliance Bladder 44 0.752
413
P INF032 Infertility 60 0.752
414
P ALP008 Alopecia 53 0.752
415
ACQ007 Acquired Immunodeficiency Syndrome 58 0.745
416
BSL008 Basal Ganglia Disease 41 0.741
417
CRH001 Crohn's Disease 80 0.741
418
c LYM145 Lymphatic Malformation 5 48 0.738
419
HSH003 Hashimoto Thyroiditis 60 0.738
420
LPT014 Leptin Deficiency or Dysfunction 77 0.738
421
DYS192 Dystonia, Dopa-Responsive 56 0.738
422
MLG169 Malignant Astrocytoma 57 0.738
423
P THR015 Thrombophilia 51 0.738
424
NSP002 Nasopharyngitis 45 0.738
425
MRG007 Morgellons 15 0.738
426
P DBT005 Diabetes Insipidus 54 0.738
427
P ASP001 Asperger Syndrome 48 0.730
428
NRL016 Neural Tube Defects 80 0.723
429
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.723
430
MDD018 Middle East Respiratory Syndrome 44 0.723
431
ATH004 Athetosis 25 0.723
432
GLS013 Glossodynia 17 0.723
433
APR001 Apraxia 51 0.708
434
P SCL018 Scoliosis 57 0.708
435
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.708
436
c THY107 Thymoma, Familial 42 0.708
437
SMT004 Smith-Lemli-Opitz Syndrome 69 0.708
438
P THY023 Thymoma 64 0.708
439
CRB037 Cerebral Palsy 66 0.708
440
P PRP029 Porphyria 60 0.708
441
SPN035 Spindle Cell Sarcoma 51 0.708
442
c CHR054 Chronic Closed-Angle Glaucoma 33 0.708
443
SRC014 Sarcoma 64 0.708
444
SPC005 Speech Disorder 46 0.708
445
PPT002 Peptic Ulcer Perforation 34 0.708
446
PLM027 Pulmonary Embolism and Infarction 22 0.708
447
HRP004 Herpes Zoster 60 0.708
448
STM007 Stomatitis 52 0.708
449
P SCK005 Sickle Cell Disease 56 0.708
450
CHR281 Chronic Hiccups 29 0.708
451
CNV002 Conversion Disorder 47 0.698
452
BSL009 Basal Ganglia Calcification 45 0.692
453
WLL001 Williams-Beuren Syndrome 60 0.692
454
GST009 Gastroschisis 53 0.692
455
P PNC035 Pancreatic Cancer 87 0.692
456
P TTR001 Tetralogy of Fallot 69 0.692
457
c SCH056 Schizophrenia 15 38 0.692
458
MNN043 Meningioma, Familial 79 0.692
459
LTN029 Latent Autoimmune Diabetes in Adults 38 0.692
460
PRM003 Premature Ejaculation 44 0.692
461
BLR008 Bilirubin Metabolic Disorder 57 0.692
462
P RTN022 Retinal Vein Occlusion 54 0.692
463
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.692
464
P CND004 Candidiasis 57 0.692
465
SCR001 Secretory Meningioma 40 0.692
466
INT395 Intracranial Meningioma 47 0.692
467
ABD010 Abdominal Wall Defect 37 0.692
468
SPS057 Spasticity 43 0.692
469
OBS003 Obsessive-Compulsive Personality Disorder 43 0.681
470
P FML011 Familial Adenomatous Polyposis 70 0.674
471
VTM002 Vitamin B12 Deficiency 48 0.674
472
MCS002 Mucositis 55 0.674
473
FCL014 Focal Epilepsy 53 0.674
474
LYM027 Lymphopenia 56 0.674
475
P ADN016 Adenocarcinoma 63 0.674
476
c ESS001 Essential Tremor 56 0.674
477
P GST044 Gastritis 55 0.674
478
CNT016 Central Retinal Vein Occlusion 53 0.674
479
DMY004 Demyelinating Disease 50 0.674
480
PCD001 Pica Disease 38 0.674
481
P HMC002 Homocystinuria 52 0.674
482
SPN186 Spinal Cord Injury 60 0.674
483
DSS010 Dissociative Disorder 39 0.662
484
P GLL020 Gallbladder Disease 57 0.655
485
VLC001 Velocardiofacial Syndrome 57 0.655
486
P PRS040 Prostate Cancer 95 0.655
487
OST159 Osteogenic Sarcoma 66 0.655
488
c SCH083 Schizophrenia 7 29 0.655
489
GLB001 Gilbert Syndrome 53 0.655
490
PRP080 Peripheral Artery Disease 54 0.655
491
GNG013 Gingivitis 59 0.655
492
P BRS044 Breast Adenocarcinoma 58 0.655
493
CHR074 Choriocarcinoma 46 0.655
494
UTR043 Uterine Sarcoma 40 0.655
495
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.655
496
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 0.651
497
AMD002 Amed Syndrome, Digenic 36 0.651
498
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 0.651
500
GLC025 Galactorrhoea-Hyperprolactinaemia 22 0.651
501
ART140 Arteries, Anomalies of 52 0.633
502
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 0.633
503
LPP008 Lipoprotein Quantitative Trait Locus 65 0.633
504
P PLM037 Pulmonary Hypertension 69 0.633
506
P LNG032 Lung Cancer 98 0.633
507
MLD001 Melioidosis 67 0.633
508
c ACT249 Acute Asthma 40 0.633
509
INT067 Interstitial Nephritis 46 0.633
510
P VNT002 Ventricular Septal Defect 58 0.633
511
MCL006 Macular Retinal Edema 56 0.633
512
P AGN002 Agnosia 53 0.633
513
MLT006 Multidrug-Resistant Tuberculosis 47 0.633
514
ACT003 Acute Kidney Tubular Necrosis 46 0.633
515
DTR001 Detrusor Sphincter Dyssynergia 37 0.633
516
GND002 Gender Identity Disorder 40 0.633
517
P PRN023 Prion Disease 60 0.633
518
MSL001 Measles 61 0.633
519
MTS001 Mutism 44 0.618
520
c SCH075 Schizophrenia 19 36 0.609
521
P CLC063 Celiac Disease 1 65 0.609
522
c CRN139 Cornelia De Lange Syndrome 1 61 0.609
523
WLF001 Wolff-Parkinson-White Syndrome 63 0.609
524
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.609
525
CNS002 Constrictive Pericarditis 39 0.609
526
P EYD002 Eye Disease 57 0.609
527
P NRM002 Normal Pressure Hydrocephalus 49 0.609
528
GLC008 Glucose Metabolism Disease 40 0.609
529
HYP043 Hyperandrogenism 47 0.609
530
P CRN015 Cornelia De Lange Syndrome 67 0.609
531
P CRD246 Cardiovascular System Disease 55 0.609
532
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.609
533
PRM020 Premenstrual Tension 39 0.609
534
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.609
535
FND002 Fundus Dystrophy 54 0.609
536
HRP009 Herpes Simplex Encephalitis 58 0.609
537
MTR086 Motor Stereotypies 14 0.609
538
c INH030 Inherited Retinal Disorder 28 0.609
539
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.609
540
P HYP730 Hypogonadotropic Hypogonadism 57 0.588
541
MLD017 Mal De Debarquement Syndrome 33 0.581
542
SCR037 Sucrase-Isomaltase Deficiency, Congenital 48 0.581
543
P PRP003 Porphyria Cutanea Tarda 66 0.581
544
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.581
545
P EPL140 Epilepsy, Idiopathic Generalized 60 0.581
546
P CYS018 Cystitis 58 0.581
547
P AGM001 Agammaglobulinemia 67 0.581
548
INS001 Insulinoma 59 0.581
549
MST005 Mastitis 52 0.581
550
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.581
551
HYD002 Hydronephrosis 58 0.581
552
P SBR004 Seborrheic Dermatitis 44 0.581
553
BNG077 Benign Idiopathic Neonatal Seizures 23 0.581
554
SPC030 Specific Language Disorder 25 0.581
555
PRD004 Prediabetes Syndrome 52 0.550
556
P NRV007 Nervous System Disease 65 0.550
557
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 0.543
558
P ASP006 Aspergillosis 71 0.543
559
BRK010 Burkitt Lymphoma 65 0.543
560
INT030 Intracranial Aneurysm 55 0.543
561
CLN015 Colon Adenocarcinoma 64 0.543
562
PYL004 Pyelitis 37 0.543
563
MCL057 Macular Dystrophy with Central Cone Involvement 28 0.543
564
HYP006 Hypertensive Heart Disease 48 0.543
565
PDP001 Pedophilia 28 0.543
566
P GLM007 Glomerulonephritis 59 0.543
567
BLD131 Bladder Urothelial Carcinoma 59 0.543
568
P CMM008 Communicating Hydrocephalus 44 0.543
569
P PRL003 Proliferative Glomerulonephritis 43 0.543
570
ACT079 Acute Proliferative Glomerulonephritis 38 0.543
571
CMM005 Common Cold 55 0.543
572
OLG001 Oligospermia 45 0.543
573
LFT001 Left Bundle Branch Hemiblock 47 0.543
574
P MLN008 Melanoma 75 0.543
575
HPT022 Hepatoblastoma 54 0.543
576
YLL002 Yellow Fever 61 0.543
577
P TMP001 Temporal Lobe Epilepsy 49 0.540
578
P NRC002 Narcolepsy 55 0.493
579
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.460
580
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.460
581
P NJM001 Nijmegen Breakage Syndrome 75 0.460
582
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.460
583
c HYP272 Hypercholesterolemia, Familial, 3 46 0.460
584
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.460
585
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 0.460
586
ANG049 Angioedema Induced by Ace Inhibitors 38 0.460
587
IMM240 Immunodeficiency 14a, Autosomal Dominant 52 0.460
588
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.460
589
HYP555 Hypertriglyceridemia, Transient Infantile 39 0.460
590
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.460
591
IMM102 Immunodeficiency 14 51 0.460
592
HYP458 Hyper Ige Syndrome 60 0.460
593
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.460
594
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.460
595
c CNT035 Central Nervous System Disease 53 0.460
596
HYP081 Hypolipoproteinemia 49 0.460
597
CRB009 Cerebritis 43 0.460
598
ACT055 Actinomycosis 54 0.460
599
49X006 49, Xxxxy Syndrome 40 0.460
600
SDD004 Sudden Arrhythmia Death Syndrome 22 0.460
601
c DWL002 Dowling-Degos Disease 1 58 0.453
602
APR010 Apraxia of Eyelid Opening 15 0.453
603
PTC002 Potocki-Lupski Syndrome 51 0.453
604
PRG014 Progesterone Resistance 42 0.453
605
MRL006 Meralgia Paraesthetica, Familial 27 0.453
606
LWG006 Low Grade Glioma 41 0.453
607
NRL005 Neurilemmoma 60 0.453
608
ADN009 Adenosquamous Carcinoma 49 0.453
609
P SKN015 Skin Carcinoma 71 0.453
610
ACS001 Acoustic Neuroma 55 0.453
611
GST008 Gastric Adenosquamous Carcinoma 19 0.453
612
PYM001 Pyomyositis 42 0.453
613
BCK018 Bickerstaff Brainstem Encephalitis 20 0.453
614
DPS001 Dipsogenic Diabetes Insipidus 21 0.450
615
PTH002 Pathological Gambling 48 0.441
616
P FRG001 Fragile X Syndrome 70 0.432
617
OPT003 Opiate Dependence 49 0.432
618
APH002 Aphasia 55 0.403
619
DPR002 Depersonalization Disorder 41 0.393
620
P DYS021 Dysautonomia 38 0.393
621
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.371
622
BRN009 Burning Mouth Syndrome 51 0.371
623
P LTR001 Lateral Sclerosis 57 0.371
624
c PRC016 Pre-Eclampsia 64 0.371
625
LNG099 Lung Disease 62 0.371
626
ERY003 Erythema Multiforme 56 0.360
627
IRN002 Iron Metabolism Disease 56 0.360
628
MTB004 Metabolic Acidosis 48 0.349
629
ATM095 Autoimmune Disease 61 0.349
630
P MYP006 Myopia 55 0.349
631
ATY001 Atypical Depressive Disorder 45 0.349
632
RMS001 Rem Sleep Behavior Disorder 47 0.349
633
c ATM075 Autoimmune Encephalitis 39 0.349
634
GTR002 Goiter 52 0.337
635
ACR007 Acromegaly 70 0.325
636
PRS021 Prostatic Adenoma 43 0.325
637
CYC005 Cyclothymic Disorder 40 0.325
638
P NRP001 Neuropathy 59 0.325
639
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.325
640
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.325
641
c GRV008 Graves Disease 1 54 0.312
642
P ECL001 Eclampsia 52 0.312
643
SMT006 Somatoform Disorder 50 0.312
644
P HYP024 Hypoparathyroidism 55 0.312
645
ATS010 Autosomal Recessive Disease 42 0.299
646
PRS129 Prostatic Hyperplasia, Benign 48 0.299
647
CRT033 Corticobasal Degeneration 48 0.299
648
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.285
649
c SCH061 Schizophrenia 16 24 0.285
650
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.285
651
HMP001 Hemopericardium 47 0.285
652
P PRP019 Peripheral Nervous System Disease 57 0.285
653
HPT004 Hepatic Coma 43 0.285
654
CNN001 Cannabis Dependence 37 0.285
655
P GRF003 Graft-Versus-Host Disease 71 0.270
656
SVR097 Severe Cutaneous Adverse Reaction 68 0.270
657
c SCH052 Schizophrenia 14 19 0.270
658
CHD004 Chudley-Mccullough Syndrome 47 0.270
659
PLY068 Polysubstance Abuse 41 0.270
660
HPT019 Hepatic Encephalopathy 59 0.270
661
PRP030 Purpura 54 0.270
662
c HPT001 Hepatitis C 61 0.270
663
P CRN026 Corneal Edema 42 0.270
664
PLG002 Plague 58 0.270
665
CPG001 Capgras Syndrome 26 0.270
666
P CMP008 Compartment Syndrome 49 0.270
667
PTH003 Pathologic Nystagmus 52 0.270
668
ERY066 Erythema Multiforme Major 29 0.270
669
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.255
670
c PNS012 Paine Syndrome 60 0.255
671
GST092 Gastroesophageal Reflux 59 0.255
672
CYC008 Cyclic Vomiting Syndrome 46 0.255
673
MLT157 Multiple System Atrophy 1 69 0.255
674
LMB024 Limbic Encephalitis 43 0.255
675
PNC001 Pancytopenia 52 0.255
676
PHN001 Phencyclidine Abuse 23 0.255
677
QDR001 Quadriplegia 49 0.255
678
AZS001 Azoospermia 45 0.255
679
PRT036 Peritonitis 65 0.255
680
ANS006 Anosognosia 34 0.238
681
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.238
682
P INF037 Inflammatory Bowel Disease 53 0.238
683
c HPT073 Hepatitis C Virus 70 0.238
684
PHB003 Phobia, Specific 44 0.238
685
P NPH012 Nephrotic Syndrome 61 0.238
686
LVR012 Liver Cirrhosis 62 0.238
687
P TRT010 Teratoma 50 0.238
688
HST001 Histrionic Personality Disorder 27 0.238
689
ATN004 Autonomic Neuropathy 42 0.238
690
P PRC012 Pericardial Effusion 50 0.238
691
SPR012 Separation Anxiety Disorder 41 0.238
692
c VRL007 Viral Encephalitis 50 0.238
693
P RTN016 Retinal Degeneration 52 0.238
694
P TXP001 Toxoplasmosis 59 0.238
695
c SCH073 Schizophrenia 9 25 0.221
696
TRT017 Teratoma, Ovarian 28 0.221
697
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.221
698
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.221
699
PCK003 Pick Disease of Brain 70 0.221
700
c GLL024 Gallbladder Disease 1 53 0.221
701
CHR669 Chromosome 2p16.3 Deletion Syndrome 22 0.221
702
DSS009 Disseminated Intravascular Coagulation 56 0.221
703
SCH004 Schizoid Personality Disorder 27 0.221
704
PRN010 Paranoid Personality Disorder 26 0.221
705
P RCT021 Rectum Cancer 54 0.221
706
P DRR001 Diarrhea 55 0.221
707
ASP008 Aspiration Pneumonitis 43 0.221
708
OVR109 Ovarian Germ Cell Teratoma 32 0.221
709
P MTR014 Motor Neuron Disease 65 0.221
710
P PLY019 Polyneuropathy 52 0.221
711
P ANT006 Antiphospholipid Syndrome 55 0.221
712
ECH002 Echolalia 33 0.221
713
PLM010 Pulmonary Edema 54 0.221
714
P NMN002 Niemann-Pick Disease 60 0.221
715
DCB001 Decubitus Ulcer 61 0.221
716
NNT008 Neonatal Abstinence Syndrome 41 0.221
717
ELC001 Elective Mutism 22 0.221
718
RRM016 Rare Movement Disorder 15 0.221
719
SMN008 Semantic Dementia 46 0.221
720
THY029 Thyroid Carcinoma 55 0.221
721
c NMN014 Niemann-Pick Disease, Type C2 49 0.201
722
CRV043 Cervical Dystonia 46 0.201
723
CRB011 Cerebrotendinous Xanthomatosis 64 0.201
724
WRN002 Wernicke-Korsakoff Syndrome 49 0.201
725
XNT003 Xanthomatosis 48 0.201
726
P DRM053 Dermatitis, Atopic 65 0.201
727
c SCH084 Schizophrenia 8 27 0.201
728
ART002 Arts Syndrome 66 0.201
729
P USH001 Usher Syndrome 63 0.201
730
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.201
731
P LKM062 Leukemia, Acute Lymphoblastic 69 0.201
732
EXH001 Exhibitionism 25 0.201
733
P HYP069 Hyperparathyroidism 62 0.201
734
P BRB001 Beriberi 44 0.201
735
PRP016 Paraplegia 52 0.201
736
c VRL010 Viral Hepatitis 52 0.201
737
KLV001 Kluver-Bucy Syndrome 34 0.201
738
TRN007 Transsexualism 38 0.201
739
KLP001 Kleptomania 36 0.201
740
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.201
741
P ESN008 Eosinophilic Pneumonia 50 0.201
742
P VSC011 Vasculitis 61 0.201
743
PRD002 Periodic Limb Movement Disorder 33 0.201
744
ULC004 Ulcerative Colitis 74 0.201
745
PST053 Postherpetic Neuralgia 39 0.201
746
BCK006 Back Pain 43 0.201
747
FMR019 Fmr1 Disorders 13 0.201
749
MLT116 Multiple System Atrophy, Parkinsonian Type 29 0.201
751
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.180
752
RTN017 Retinal Detachment 60 0.180
753
P RTT002 Rett Syndrome 79 0.180
754
IFP003 Ifap Syndrome 2 41 0.180
755
CYN002 Cyanosis, Transient Neonatal 43 0.180
756
c NMN015 Niemann-Pick Disease, Type C1 68 0.180
757
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.180
758
P ORT004 Orthostatic Intolerance 61 0.180
759
PHL006 Phelan-Mcdermid Syndrome 61 0.180
760
PRS119 Persistent Genital Arousal Disorder 18 0.180
761
CHL123 Chlamydia 58 0.180
762
CRD001 Cardiac Tamponade 44 0.180
763
P PRT026 Parotitis 42 0.180
764
P OLG002 Oligodendroglioma 66 0.180
765
WRN003 Wernicke Encephalopathy 45 0.180
766
CRB033 Cerebral Degeneration 36 0.180
767
GST037 Gastroparesis 52 0.180
768
DRM006 Dermatitis 61 0.180
769
ULN001 Ulnar Neuropathy 28 0.180
770
URM002 Uremia 47 0.180
771
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.180
772
P MCR010 Microcephaly 59 0.180
773
RGH001 Right Bundle Branch Block 47 0.180
774
CYS005 Cysticercosis 60 0.180
775
P INF038 Influenza 68 0.180
776
P ALP009 Alopecia Areata 59 0.180
777
PSY017 Psychogenic Movement Disorders 22 0.180
778
OGL001 Ogilvie Syndrome 24 0.180
779
SPL018 Splenomegaly 47 0.180
780
P FBR031 Febrile Seizures 52 0.180
781
FLP002 Floppy Infant Syndrome 13 0.180
782
MLR004 Malaria 77 0.156
783
DFC004 Deficiency Anemia 74 0.156
784
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.156
785
P PRG013 Paraganglioma 57 0.156
786
SGM008 Segmental Dystonia 28 0.156
787
SCN049 Second-Degree Atrioventricular Block 34 0.156
788
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.156
789
MBS002 Moebius Syndrome 53 0.156
790
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.156
791
P OVR042 Ovarian Cancer 88 0.156
792
SMT008 Smith-Magenis Syndrome 53 0.156
794
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.156
795
c LKM061 Leukemia, Acute Myeloid 83 0.156
796
BLP048 Blepharospasm, Benign Essential 36 0.156
797
SYD002 Sydenham Chorea 34 0.156
798
FTL006 Fetal Alcohol Spectrum Disorder 43 0.156
799
P MTC003 Metachromatic Leukodystrophy 71 0.156
800
P LPR021 Leprosy 3 71 0.156
801
DLY008 Delayed Sleep Phase Disorder 44 0.156
802
PRP009 Peripartum Cardiomyopathy 54 0.156
803
APN008 Apnea, Obstructive Sleep 66 0.156
804
THY111 Thyroid Carcinoma, Familial Medullary 67 0.156
805
CRT072 Creutzfeldt-Jakob Disease 67 0.156
806
ESP021 Esophageal Cancer 84 0.156
807
TQP001 Taqi Polymorphism 29 0.156
808
c SCH086 Schizophrenia 11 21 0.156
809
P LNG064 Lung Cancer Susceptibility 3 69 0.156
810
P SNS001 Sensorineural Hearing Loss 60 0.156
811
P MMP001 Mumps 56 0.156
812
MGC001 Megacolon 48 0.156
813
P DDN001 Duodenal Ulcer 52 0.156
814
P LKM002 Leukemia 65 0.156
815
PHR003 Pharyngitis 57 0.156
816
THR004 Thrombocytosis 52 0.156
817
INT071 Intestinal Perforation 49 0.156
818
FCT008 Factitious Disorder 34 0.156
819
ACT078 Acute Porphyria 50 0.156
820
MYL001 Myelitis 49 0.156
821
P CYS017 Cystic Teratoma 41 0.156
822
FDL002 Food Allergy 47 0.156
823
HYP014 Hyperuricemia 51 0.156
824
P TBR001 Tuberous Sclerosis 69 0.156
825
P OTS001 Otosclerosis 49 0.156
826
P MLN007 Male Infertility 56 0.156
827
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.156
828
P ISL078 Isolated Ectopia Lentis 58 0.156
829
HRY002 Hairy Tongue 28 0.156
830
MTR010 Mature Teratoma 40 0.156
831
GST045 Gastroenteritis 58 0.156
832
P END033 Endocarditis 58 0.156
833
HRT012 Heart Valve Disease 53 0.156
834
THY125 Thyroid Gland Medullary Carcinoma 48 0.156
835
ART016 Aortic Aneurysm 68 0.156
836
MNN009 Meningoencephalitis 47 0.156
837
P LKD001 Leukodystrophy 58 0.156
838
END062 Endometrial Hyperplasia 47 0.156
839
c BNG093 Benign Teratoma 39 0.156
840
TNG007 Tongue Carcinoma 55 0.156
841
P GND004 Gonadal Dysgenesis 46 0.156
842
DMP001 Dumping Syndrome 43 0.156
843
CHL013 Cholecystolithiasis 37 0.156
844
GT001 Gout 63 0.156
845
SCB001 Scabies 49 0.156
846
P HML002 Hemolytic Anemia 62 0.156
847
PHB001 Phobic Disorder 45 0.156
848
c INH020 Inherited Metabolic Disorder 47 0.156
849
BRN024 Bronchitis 67 0.156
850
AMP007 Amphetamine Abuse 36 0.156
851
P MYL006 Myeloid Leukemia 60 0.156
852
P RBL001 Rubella 58 0.156
853
CLF001 Cleft Lip 54 0.156
854
PTY001 Pityriasis Rosea 44 0.156
855
PLY012 Polyhydramnios 46 0.156
856
HNS001 Hansen's Disease 32 0.156
857
ADC009 Adcy5 Dyskinesia 8 0.156
858
HMP009 Haemophilus Influenzae 41 0.156
859
RTR011 Retroperitoneal Fibrosis 47 0.156
860
RFR003 Refractive Error 41 0.156
861
HRN003 Heroin Dependence 44 0.156
862
P PHC019 Pheochromocytoma-Paraganglioma 35 0.156
863
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.156
864
ARG004 Argyria 26 0.156
865
CRD137 Cardiogenic Shock 56 0.156
866
VSL003 Visual Agnosia 33 0.127
867
ALL003 Allergic Rhinitis 66 0.127
868
c LPR022 Leprosy 2 35 0.127
869
ATY003 Atypical Autism 35 0.127
870
c PRM108 Primary Progressive Multiple Sclerosis 51 0.127
871
P MTR004 Maturity-Onset Diabetes of the Young 66 0.127
872
P LYM118 Lymphoma 66 0.127
873
ING001 Inguinal Hernia 59 0.127
874
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.127
875
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.127
876
c ANM038 Anemia, Autoimmune Hemolytic 63 0.127
877
P MDL005 Medulloblastoma 75 0.127
878
OTT002 Otitis Media 70 0.127
879
DSC013 Discrimination, Two-Point, Reduction in 21 0.127
880
ERY029 Erythermalgia, Primary 57 0.127
881
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.127
882
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.127
883
P RTN024 Retinoblastoma 72 0.127
884
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 48 0.127
885
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.127
886
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 44 0.127
887
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.127
888
P GLC113 Galactosemia I 65 0.127
889
TRP006 Tarp Syndrome 58 0.127
890
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.127
891
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.127
892
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.127
893
SPC010 Speech and Communication Disorders 47 0.127
894
HYP025 Hyperphosphatemia 47 0.127
895
FML037 Female Breast Cancer 51 0.127
896
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.127
897
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 0.127
898
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.127
899
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.127
900
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.127
901
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.127
902
ABT001 Abetalipoproteinemia 68 0.127
903
ARC025 Arachnoid Cysts, Intracranial 37 0.127
904
DND001 Dandy-Walker Syndrome 48 0.127
905
c TBR025 Tuberous Sclerosis 1 84 0.127
906
c DPH024 Diaphragmatic Hernia, Congenital 63 0.127
907
TRG002 Trigeminal Neuralgia 61 0.127
908
KLN009 Kleine-Levin Hibernation Syndrome 37 0.127
909
PHN003 Phenylketonuria 76 0.127
910
SDD001 Sudden Infant Death Syndrome 60 0.127
911
P STR020 Strabismus 56 0.127
912
ART103 Arthrogryposis, Mental Retardation, and Seizures 37 0.127
913
c LKM063 Leukemia, Chronic Myeloid 70 0.127
914
ACN002 Acanthosis Nigricans 56 0.127
915
MRF001 Marfan Syndrome 76 0.127
916
P MYS005 Myositis 55 0.127
917
NTR018 Neutrophilia, Hereditary 49 0.127
918
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.127
919
P FTL001 Fetal Alcohol Syndrome 55 0.127
920
OPD001 Opioid Abuse 44 0.127
921
P TRN034 Transverse Myelitis 47 0.127
922
SLD003 Sialadenitis 47 0.127
923
c VRL012 Viral Meningitis 46 0.127
924
CLN003 Clonorchiasis 42 0.127
925
P ACT028 Acute Closed-Angle Glaucoma 32 0.127
926
P SCK002 Sick Sinus Syndrome 55 0.127
927
HYP085 Hypothalamic Disease 38 0.127
928
TRC003 Trichomoniasis 53 0.127
929
CHL067 Cholecystitis 59 0.127
930
KRT009 Keratosis 52 0.127
931
STR103 Streptococcus Pneumonia 47 0.127
932
P PYL005 Pyelonephritis 56 0.127
933
IDM001 Ideomotor Apraxia 37 0.127
934
CLL003 Cellulitis 53 0.127
935
CMP010 Complex Regional Pain Syndrome 59 0.127
936
NPH009 Nephrolithiasis 54 0.127
937
CNN005 Connective Tissue Disease 66 0.127
938
OVR063 Overnutrition 42 0.127
939
GLS007 Glossitis 46 0.127
940
VSC064 Vascular Parkinsonism 20 0.127
941
P OPT006 Optic Nerve Disease 57 0.127
942
CRN019 Coronary Artery Vasospasm 47 0.127
943
CHL012 Childhood Disintegrative Disease 44 0.127
944
DRY001 Dry Eye Syndrome 49 0.127
945
BRC012 Brucellosis 66 0.127
946
P END044 Endometriosis 62 0.127
947
ENT004 Enthesopathy 51 0.127
948
c HPT016 Hepatitis B 62 0.127
949
P PSD015 Pseudohypoparathyroidism 54 0.127
950
INT066 Interstitial Lung Disease 60 0.127