Search results for Dopamine

2529 hits were found for Dopamine

# Family MCID Name MIFTS Score
1
DPM001 Dopamine Beta-Hydroxylase Deficiency 53 43.815
2
P PRK039 Parkinsonism 55 39.634
3
P PRK057 Parkinson Disease, Late-Onset 80 36.657
4
P ATT013 Attention Deficit-Hyperactivity Disorder 64 30.978
5
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 27.810
6
P SCH015 Schizophrenia 74 26.572
7
c ORT011 Orthostatic Hypotension 1 43 23.488
8
P TRM003 Tremor 48 22.063
9
ALC007 Alcohol Dependence 66 20.769
10
P DYS154 Dystonia 64 19.367
11
TRD006 Tardive Dyskinesia 53 19.321
12
HYP020 Hyperprolactinemia 63 19.302
13
P MVM001 Movement Disease 61 18.812
14
PRT037 Pertussis 65 18.288
15
P BPL003 Bipolar Disorder 56 17.900
16
P PHC003 Pheochromocytoma 69 17.666
17
ADR040 Adrenal Gland Pheochromocytoma 46 17.624
18
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 17.563
19
P NRB001 Neuroblastoma 66 17.258
20
P HNT016 Huntington Disease 73 16.891
21
c MJR022 Major Affective Disorder 8 38 16.817
22
c MJR024 Major Affective Disorder 9 41 16.817
23
P RST001 Restless Legs Syndrome 52 16.594
24
CCN002 Cocaine Abuse 49 16.274
25
BRN112 Brain Dopamine-Serotonin Vesicular Transport Disease 18 16.137
26
P SBS003 Substance Abuse 54 15.841
27
PTT037 Pituitary Tumors 44 15.361
28
c HYP595 Hypertension, Essential 85 15.108
29
ADN018 Adenoma 59 14.697
30
MNT002 Mental Depression 57 14.675
31
TXC005 Toxic Shock Syndrome 62 14.478
32
DPR016 Depression 65 14.196
34
PSY004 Psychotic Disorder 66 13.747
35
P MJR001 Major Depressive Disorder 68 13.713
36
PRK102 Parkinsonism-Dystonia, Infantile, 2 26 13.538
37
TBC004 Tobacco Addiction 63 13.277
38
P ALC033 Alcohol Use Disorder 61 12.957
39
MDD011 Mood Disorder 62 12.713
40
PTH002 Pathological Gambling 48 12.531
41
P PTT006 Pituitary Adenoma 55 12.504
42
OBS002 Obsessive-Compulsive Disorder 68 12.208
43
CCN001 Cocaine Dependence 48 12.202
44
PRT058 Pure Autonomic Failure 58 12.142
45
c ACT071 Acute Kidney Failure 60 12.004
46
GLL008 Gilles De La Tourette Syndrome 65 11.980
47
P SMK004 Smoking As a Quantitative Trait Locus 3 44 11.849
48
MLT157 Multiple System Atrophy 1 69 11.721
49
ACR007 Acromegaly 70 11.515
50
CHR073 Choreatic Disease 54 11.373
51
DPM008 Dopamine Beta-Hydroxylase, Plasma, Thermolability of 5 11.296
52
DRG003 Drug Dependence 46 10.679
53
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 10.657
54
ETN001 Eating Disorder 59 10.500
55
WTH001 Withdrawal Disorder 48 10.198
56
AGN016 Aging 54 10.141
57
CHL014 Cholera 62 10.016
58
PST028 Post-Traumatic Stress Disorder 59 9.878
59
TRM010 Traumatic Brain Injury 51 9.825
60
c MGR028 Migraine with or Without Aura 1 64 9.730
61
P TCD001 Tic Disorder 49 9.663
62
BRN071 Brain Injury 50 9.630
63
ANX010 Anxiety 70 9.591
64
CRD137 Cardiogenic Shock 56 9.334
65
HYP266 Hypoxia 57 9.314
66
P MYP006 Myopia 56 9.298
67
P KDN018 Kidney Disease 72 9.248
68
c ATS007 Autism Spectrum Disorder 72 9.242
69
PNG002 Pain Agnosia 51 9.214
70
ALL029 Allergic Disease 59 9.163
71
P SPR120 Supranuclear Palsy, Progressive, 1 69 9.095
72
48X005 48,xyyy 39 9.090
73
P ATS364 Autism 69 9.041
74
c ESS001 Essential Tremor 57 8.882
75
IRN002 Iron Metabolism Disease 57 8.717
76
P ENC018 Encephalopathy 62 8.674
77
P SLP005 Sleep Disorder 61 8.659
78
P SZR006 Seizure Disorder 70 8.426
79
P DMN002 Dementia 66 8.330
80
P NRC002 Narcolepsy 56 8.320
81
P CHR345 Chronic Pain 50 8.255
82
ACT084 Acute Stress Disorder 54 8.202
83
NRL004 Neuroleptic Malignant Syndrome 52 8.172
84
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 8.060
85
P ALZ034 Alzheimer Disease 87 8.016
86
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 8.010
87
P PRS038 Personality Disorder 65 7.984
88
ANR007 Anorexia Nervosa 60 7.874
89
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 7.779
90
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 7.779
91
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 7.779
92
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 7.779
93
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 7.779
94
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 7.779
95
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 7.779
96
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 7.779
97
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 7.779
98
CNG034 Congestive Heart Failure 69 7.685
99
HYP056 Hypoglycemia 65 7.684
100
HLX001 Helix Syndrome 48 7.596
101
OPD006 Opioid Addiction 48 7.558
102
PPL052 Papillomatosis, Confluent and Reticulated 34 7.557
103
ATN005 Autonomic Dysfunction 46 7.527
104
OPT003 Opiate Dependence 49 7.518
105
RMS001 Rem Sleep Behavior Disorder 47 7.457
106
SCH012 Schizoaffective Disorder 50 7.442
107
SBC016 Subacute Delirium 43 7.422
108
IMP006 Impulse Control Disorder 45 7.379
109
HYP066 Hyperglycemia 61 7.315
110
P PTS002 Ptosis 52 7.088
111
IMP005 Impotence 52 7.041
112
P HYP086 Hypothyroidism 69 7.041
113
GLC096 Galactorrhea 40 6.971
114
CNS004 Constipation 56 6.961
115
SXL003 Sexual Disorder 49 6.920
116
P MJR007 Major Affective Disorder 1 42 6.899
117
HRT012 Heart Valve Disease 53 6.894
118
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 6.855
119
RPD005 Rapidly Involuting Congenital Hemangioma 46 6.822
120
END040 Endogenous Depression 55 6.797
121
AMN003 Amnestic Disorder 54 6.759
122
HYP060 Hyperinsulinism 54 6.560
123
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 56 6.519
124
SBS004 Substance Dependence 47 6.498
125
PHN003 Phenylketonuria 76 6.472
126
AMN001 Amenorrhea 54 6.423
127
P HRT032 Heart Disease 81 6.399
128
P MYC033 Myoclonus 47 6.299
129
HPT004 Hepatic Coma 43 6.227
130
P LTR001 Lateral Sclerosis 58 6.200
131
OVR029 Ovarian Hyperstimulation Syndrome 63 6.200
132
ANX004 Anoxia 40 6.168
133
HPT019 Hepatic Encephalopathy 59 6.168
134
HYP080 Hypogonadism 50 6.160
135
LSC001 Lesch-Nyhan Syndrome 62 6.141
136
FBR047 Fibromyalgia 58 6.141
137
c AMY091 Amyotrophic Lateral Sclerosis 1 88 6.138
138
P HDC001 Headache 57 6.138
139
MLD018 Mild Cognitive Impairment 48 6.002
140
P RSP003 Respiratory Failure 74 5.932
141
P CRD119 Cardiac Arrest 67 5.876
142
GLM045 Glioma 63 5.775
143
GLL048 Glial Tumor 52 5.750
144
P NRP001 Neuropathy 60 5.744
145
OCL069 Ocular Motor Apraxia 57 5.676
146
P DDN001 Duodenal Ulcer 53 5.661
147
P PRG013 Paraganglioma 57 5.502
148
BLM002 Bulimia Nervosa 57 5.469
149
P HYP265 Hypotonia 42 5.424
150
CRB004 Cerebral Artery Occlusion 45 5.373
151
CRB039 Cerebrovascular Disease 66 5.336
152
MRP001 Morphine Dependence 42 5.331
153
P HYP083 Hypopituitarism 52 5.325
154
SPN186 Spinal Cord Injury 61 5.323
155
P PTN014 Patent Ductus Arteriosus 1 59 5.310
156
47X002 47,xyy 48 5.304
157
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 5.278
158
HRW001 Hair Whorl 35 5.277
159
HRN003 Heroin Dependence 44 5.266
160
CRT033 Corticobasal Degeneration 47 5.240
161
TTN003 Tetanus 65 5.237
162
P DYS021 Dysautonomia 38 5.225
163
STR067 Stroke, Ischemic 80 5.224
164
PLY068 Polysubstance Abuse 41 5.211
165
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.207
166
c TYP009 Type 2 Diabetes Mellitus 92 5.197
167
MNG007 Manganese Poisoning 28 5.194
168
ISC004 Ischemia 61 5.182
169
GLB002 Glioblastoma 67 5.153
170
CRB037 Cerebral Palsy 67 5.122
171
P PLY011 Polycystic Ovary Syndrome 57 5.105
172
WLS001 Wilson Disease 70 5.089
173
DMN031 Dementia, Lewy Body 65 5.051
174
P EPL164 Epilepsy 68 5.038
175
PLM010 Pulmonary Edema 55 5.037
176
P FML187 Familial Hypertension 34 5.001
177
CYT002 Cytokine Deficiency 43 4.977
178
PRN009 Paranoid Schizophrenia 49 4.948
179
CND002 Conduct Disorder 51 4.909
180
OPD001 Opioid Abuse 44 4.895
181
RFR003 Refractive Error 41 4.853
182
c ATR087 Atrial Standstill 1 74 4.813
183
GST037 Gastroparesis 52 4.801
184
c BPL002 Bipolar I Disorder 47 4.790
185
LNG015 Lingual-Facial-Buccal Dyskinesia 47 4.725
186
TQP001 Taqi Polymorphism 29 4.712
187
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 4.699
188
INS024 Insulin-Like Growth Factor I 78 4.695
189
PST092 Posttransplant Acute Limbic Encephalitis 28 4.691
190
c DLT002 Dilated Cardiomyopathy 78 4.685
191
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 4.669
192
P PLM037 Pulmonary Hypertension 72 4.656
193
LVR012 Liver Cirrhosis 63 4.559
194
P RTT002 Rett Syndrome 79 4.555
195
MTB004 Metabolic Acidosis 48 4.514
196
P HYP076 Hyperthyroidism 53 4.512
197
BRN004 Brain Edema 54 4.501
198
c SCH079 Schizophrenia 1 44 4.482
199
IMM167 Immune Deficiency Disease 78 4.469
200
VSC002 Vascular Dementia 60 4.452
201
P ENC004 Encephalitis 61 4.441
202
GLC003 Glucose Intolerance 54 4.428
203
P INF032 Infertility 57 4.404
204
SCH011 Schizotypal Personality Disorder 36 4.387
205
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.371
206
P MGR001 Migraine Without Aura 49 4.350
207
AMP007 Amphetamine Abuse 36 4.334
208
SCH003 Schizophreniform Disorder 55 4.310
209
FCL022 Focal Dystonia 42 4.299
210
P MGR003 Migraine with Aura 52 4.279
211
ANG054 Angina Pectoris 66 4.278
212
P ADL010 Adult Respiratory Distress Syndrome 71 4.278
213
SRT004 Serotonin Syndrome 54 4.266
214
P PNC025 Panic Disorder 52 4.232
215
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.221
216
CRT015 Carotid Artery Occlusion 45 4.221
217
HYP005 Hypokalemia 55 4.212
218
P DBT009 Diabetes Mellitus 67 4.202
219
c ACT075 Acute Myocardial Infarction 56 4.199
220
FRN006 Frontotemporal Dementia 68 4.198
221
VSC064 Vascular Parkinsonism 21 4.187
222
P PRM227 Primary Orthostatic Hypotension 24 4.184
223
P SLP006 Sleep Apnea 69 4.184
224
STT041 Stuttering 52 4.173
225
c MCR115 Microvascular Complications of Diabetes 5 65 4.170
226
IRR002 Irritable Bowel Syndrome 65 4.140
227
c CHR684 Chronic Kidney Disease 69 4.110
228
SYN036 Syncope 45 4.109
229
c ACT027 Acute Pancreatitis 60 4.102
230
c TYP008 Type 1 Diabetes Mellitus 70 4.102
231
LPD008 Lipid Metabolism Disorder 62 4.090
232
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 4.070
233
c ERL056 Early-Onset Parkinson's Disease 40 4.047
234
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 18 4.038
235
c CNT035 Central Nervous System Disease 54 4.031
236
P END044 Endometriosis 62 4.025
237
P GLM040 Glioma Susceptibility 1 71 4.010
238
c PRC016 Pre-Eclampsia 65 4.010
239
ALL014 Allergic Encephalomyelitis 34 3.994
240
DFC004 Deficiency Anemia 74 3.978
241
CNN001 Cannabis Dependence 38 3.973
242
MLT116 Multiple System Atrophy, Parkinsonian Type 29 3.972
243
P RTN016 Retinal Degeneration 52 3.971
244
P RNL015 Renal Hypertension 45 3.971
245
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.963
246
NRR001 Neuroretinitis 42 3.958
247
RTN023 Retinitis 46 3.958
248
HPT014 Hepatorenal Syndrome 49 3.958
249
P DRR001 Diarrhea 55 3.951
250
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.931
251
P HYD006 Hydrocephalus 61 3.891
252
AVD001 Avoidant Personality Disorder 49 3.882
253
HND015 Hand Skill, Relative 30 3.872
254
END086 End Stage Renal Disease 52 3.863
255
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.858
256
PRT036 Peritonitis 65 3.853
257
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 56 3.853
258
MLG169 Malignant Astrocytoma 57 3.846
259
DYS073 Dysphagia 53 3.833
260
RCK004 Rickets 68 3.825
261
P FRG001 Fragile X Syndrome 70 3.819
262
HMN044 Human Immunodeficiency Virus Type 1 78 3.818
263
HDN002 Head Injury 44 3.798
264
P TMP001 Temporal Lobe Epilepsy 49 3.785
265
NVL002 Novelty Seeking Personality Trait 15 3.769
266
CNN003 Conn's Syndrome 79 3.765
267
SPS057 Spasticity 42 3.735
268
P VSC007 Vascular Disease 63 3.732
269
P PRP019 Peripheral Nervous System Disease 58 3.731
270
P MLT020 Multiple Sclerosis 79 3.720
271
DLS001 Delusional Disorder 45 3.715
272
HYP141 Hyperphenylalaninemia 42 3.709
273
ACT003 Acute Kidney Tubular Necrosis 46 3.698
274
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 3.680
275
ADG002 Audiogenic Seizures 25 3.641
276
ENT011 Enterocolitis 55 3.640
277
RBS001 Rabies 58 3.636
278
P NRV007 Nervous System Disease 67 3.603
279
P NRF002 Neurofibromatosis 57 3.602
280
FNC007 Functioning Pituitary Adenoma 42 3.592
281
TRN015 Transient Cerebral Ischemia 63 3.592
282
P LCT001 Lactic Acidosis 51 3.588
283
INT075 Intracranial Hypertension 53 3.585
284
c MCR130 Microvascular Complications of Diabetes 6 41 3.577
285
c MCR120 Microvascular Complications of Diabetes 7 47 3.577
286
c MCR113 Microvascular Complications of Diabetes 3 52 3.577
287
c MCR133 Microvascular Complications of Diabetes 4 41 3.577
288
P ECL001 Eclampsia 52 3.575
289
MNK001 Menkes Disease 64 3.561
290
MLG157 Malignant Pheochromocytoma 36 3.561
291
P RTN024 Retinoblastoma 73 3.557
292
P RHM011 Rheumatoid Arthritis 82 3.541
293
PTT009 Pituitary Gland Disease 53 3.539
294
PRT251 Proteinuria, Chronic Benign 57 3.516
295
ANT011 Antisocial Personality Disorder 47 3.495
296
c CNG006 Congenital Hypothyroidism 63 3.494
297
STT001 Status Epilepticus 59 3.485
298
OCL006 Ocular Hypertension 53 3.483
299
SCL003 Social Phobia 48 3.480
300
c EXD008 Exudative Vitreoretinopathy 1 71 3.477
301
P RTN008 Retinitis Pigmentosa 80 3.476
302
BRD004 Borderline Personality Disorder 53 3.464
303
P BLP003 Blepharospasm 46 3.440
304
GST023 Gastric Ulcer 52 3.424
305
NWB001 Newborn Respiratory Distress Syndrome 56 3.423
306
CNN002 Cannabis Abuse 45 3.423
307
P STR001 Striatonigral Degeneration 37 3.411
308
P INF037 Inflammatory Bowel Disease 53 3.397
309
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.381
310
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 3.378
311
SYD002 Sydenham Chorea 34 3.357
312
NRN004 Neuroendocrine Tumor 59 3.348
313
HRT011 Heart Septal Defect 49 3.346
314
P PNC044 Pancreatitis 61 3.339
315
P TXP001 Toxoplasmosis 60 3.339
316
PRN019 Perinatal Necrotizing Enterocolitis 60 3.339
317
OPP004 Oppositional Defiant Disorder 49 3.338
318
P MLT074 Multiple Endocrine Neoplasia 59 3.323
319
ANV001 Anovulation 47 3.318
320
c PNS012 Paine Syndrome 60 3.310
321
SVR004 Severe Combined Immunodeficiency 72 3.309
322
NRT001 Neurotic Disorder 56 3.294
323
CRV043 Cervical Dystonia 46 3.283
324
P ORT004 Orthostatic Intolerance 63 3.278
325
ALD013 Aldosterone-Producing Adenoma 36 3.278
326
ARG004 Argyria 26 3.276
327
BSL008 Basal Ganglia Disease 41 3.272
328
P HRP006 Herpes Simplex 65 3.271
329
ATN004 Autonomic Neuropathy 42 3.271
330
DSS008 Disease of Mental Health 74 3.253
331
APH002 Aphasia 56 3.240
332
P LVR013 Liver Disease 69 3.234
333
DRG016 Drug Induced Dyskinesia 23 3.226
334
GNR004 Generalized Anxiety Disorder 55 3.214
335
BRX001 Bruxism 51 3.207
336
DBT010 Diabetic Neuropathy 54 3.189
337
IRN001 Iron Deficiency Anemia 58 3.183
338
PST021 Postpartum Depression 50 3.180
339
INT323 Intraocular Pressure Quantitative Trait Locus 64 3.175
340
PSD088 Pseudobulbar Affect 33 3.175
341
DWN001 Down Syndrome 70 3.163
342
P DBT005 Diabetes Insipidus 54 3.151
343
NNF007 Non-Functioning Pituitary Adenoma 39 3.148
344
PRM003 Premature Ejaculation 44 3.147
345
P OVR082 Overgrowth Syndrome 49 3.145
346
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 3.144
347
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 3.135
348
MNN043 Meningioma, Familial 79 3.125
349
P EXN002 Exanthem 58 3.121
350
c HRD198 Hereditary Dystonia 30 3.121
351
SCR001 Secretory Meningioma 40 3.102
352
LYM002 Lymphoplasmacyte-Rich Meningioma 35 3.102
353
SPN021 Spinal Meningioma 50 3.102
354
P SPN301 Spinocerebellar Ataxia 2 59 3.100
355
GRN017 Granulocytopenia 42 3.098
356
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 3.082
357
CRD223 Cardiac Arrhythmia 63 3.049
358
c INH020 Inherited Metabolic Disorder 48 3.037
359
MTR086 Motor Stereotypies 14 3.027
360
LRN003 Learning Disability 49 3.026
361
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 3.013
362
CRB090 Cerebral Hypoxia 42 3.012
363
P PRS040 Prostate Cancer 95 3.011
364
RSP019 Respiratory Distress Syndrome in Premature Infants 52 2.994
365
MTR002 Mitral Valve Insufficiency 52 2.990
366
P CRN300 Coronary Heart Disease 1 73 2.986
367
P TRT019 Torticollis 47 2.981
368
P OBS001 Obstructive Jaundice 48 2.967
369
GST092 Gastroesophageal Reflux 61 2.965
370
LPP008 Lipoprotein Quantitative Trait Locus 65 2.957
371
c CHR056 Chronic Tic Disorder 36 2.939
372
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.937
373
GNG005 Gangliocytoma 55 2.912
374
GNG002 Ganglioneuroma 52 2.887
375
P MLN008 Melanoma 76 2.883
376
CRH001 Crohn's Disease 80 2.872
377
c ACT134 Acute Liver Failure 59 2.868
378
ACQ007 Acquired Immunodeficiency Syndrome 59 2.868
379
ATS010 Autosomal Recessive Disease 42 2.861
380
CRB009 Cerebritis 43 2.860
381
URM002 Uremia 47 2.852
382
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 37 2.851
384
PTH003 Pathologic Nystagmus 52 2.850
385
P LNG032 Lung Cancer 98 2.842
386
DGR001 Digeorge Syndrome 62 2.838
387
LPT014 Leptin Deficiency or Dysfunction 78 2.836
388
FTL006 Fetal Alcohol Spectrum Disorder 43 2.836
389
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 2.821
390
CRC006 Carcinoid Syndrome 55 2.821
391
P RNV001 Renovascular Hypertension 49 2.808
392
c ERL020 Early-Onset Schizophrenia 44 2.808
393
P MTR014 Motor Neuron Disease 65 2.802
394
P BRS047 Breast Cancer 98 2.791
395
MLN003 Melancholia 41 2.789
396
RST023 Resting Heart Rate, Variation in 40 2.779
397
IGG001 Iga Glomerulonephritis 50 2.779
398
P OLV001 Olivopontocerebellar Atrophy 51 2.779
399
CHR066 Chronic Fatigue Syndrome 60 2.770
400
P PNM007 Pneumonia 67 2.764
401
PTT004 Pituitary Apoplexy 47 2.762
402
PST027 Postencephalitic Parkinson Disease 46 2.744
403
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.742
404
P NPH012 Nephrotic Syndrome 60 2.738
405
P MYC007 Myocardial Infarction 70 2.732
406
P TRT010 Teratoma 51 2.728
407
HGH043 High Grade Glioma 45 2.720
408
P PLY014 Polycystic Kidney Disease 69 2.707
409
P HYP263 Hypersomnia 41 2.691
410
HMS001 Hemosiderosis 48 2.689
411
HGH001 High Pressure Neurological Syndrome 27 2.689
412
SPP007 Suppression Amblyopia 38 2.686
413
AMB002 Amblyopia 50 2.686
414
BCK006 Back Pain 47 2.686
415
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.680
416
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.680
417
P GLM007 Glomerulonephritis 60 2.678
418
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.678
419
BRN056 Bronchopulmonary Dysplasia 56 2.673
420
P PRV006 Pervasive Developmental Disorder 52 2.669
421
P RRH023 Rare Hereditary Hemochromatosis 54 2.664
422
P VNT002 Ventricular Septal Defect 58 2.664
423
SGW002 Segawa Syndrome, Autosomal Recessive 44 2.659
424
c SML038 Small Cell Cancer of the Lung 69 2.650
425
BCT022 Bacterial Infectious Disease 56 2.639
426
MTS001 Mutism 44 2.639
427
HYP014 Hyperuricemia 51 2.625
428
ART140 Arteries, Anomalies of 53 2.612
429
ASP007 Aspiration Pneumonia 49 2.611
430
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 48 2.611
431
DBT002 Diabetic Autonomic Neuropathy 41 2.604
432
OCL010 Ocular Hypotension 37 2.597
433
P HYP098 Hypereosinophilic Syndrome 66 2.595
434
ADL002 Adult Syndrome 70 2.592
435
CYN002 Cyanosis, Transient Neonatal 43 2.586
436
ERL001 Early Myoclonic Encephalopathy 62 2.575
437
DPH001 Diphtheria 59 2.568
438
ANR004 Anuria 44 2.562
439
ATM095 Autoimmune Disease 61 2.561
440
P AMY004 Amyloidosis 70 2.555
441
PST103 Postpartum Psychosis 31 2.553
442
c DYS056 Dystonia 12 63 2.548
443
NTR005 Nutritional Deficiency Disease 61 2.547
444
PPT005 Peptic Ulcer Disease 58 2.543
445
ATR057 Atrioventricular Block 54 2.537
446
DYS009 Dysthymic Disorder 52 2.537
447
HMC014 Homocysteinemia 52 2.536
448
GYN001 Gynecomastia 47 2.536
449
INF021 Infant Gynecomastia 30 2.536
450
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.535
451
TRC022 Tricuspid Valve Insufficiency 47 2.535
452
HYP030 Hypoactive Sexual Desire Disorder 41 2.527
453
P CLS010 Cluster Headache 42 2.527
454
ANT039 Antisynthetase Syndrome 55 2.522
455
ALB002 Albinism 47 2.522
456
GRW007 Growth Hormone Deficiency 46 2.511
457
c MJR006 Major Affective Disorder 5 32 2.509
458
c MJR003 Major Affective Disorder 6 32 2.509
459
P OPN001 Open-Angle Glaucoma 55 2.505
460
P FTL001 Fetal Alcohol Syndrome 55 2.491
461
P NRM002 Normal Pressure Hydrocephalus 49 2.485
462
APR001 Apraxia 52 2.481
463
DWR001 Dwarfism 44 2.478
464
P MCH002 Machado-Joseph Disease 62 2.457
465
P HPT023 Hepatocellular Carcinoma 96 2.456
466
c BRN108 Branchiootic Syndrome 1 62 2.447
467
BRN028 Brain Cancer 74 2.439
468
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.431
469
IDP033 Idiopathic Edema 41 2.427
470
OST159 Osteogenic Sarcoma 66 2.426
471
ADS004 Aids Dementia Complex 40 2.410
472
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.409
473
P RTN018 Retinal Disease 53 2.409
474
P NRN021 Neuronal Ceroid Lipofuscinosis 65 2.396
475
THY029 Thyroid Carcinoma 51 2.383
476
JPN002 Japanese Encephalitis 61 2.383
477
P PLY019 Polyneuropathy 52 2.378
478
PRV004 Periventricular Leukomalacia 52 2.378
479
CRB033 Cerebral Degeneration 39 2.378
480
ART002 Arts Syndrome 66 2.377
481
OBS003 Obsessive-Compulsive Personality Disorder 43 2.370
482
CLB010 Coloboma of Macula 53 2.366
483
P KDN017 Kidney Cancer 61 2.365
484
AND005 Androgen Insensitivity Syndrome, Mild 21 2.347
485
P ATN002 Autonomic Nervous System Disease 51 2.343
486
SVR001 Severe Acute Respiratory Syndrome 67 2.335
487
P PSR002 Psoriasis 63 2.334
488
PST011 Pustulosis of Palm and Sole 52 2.334
489
PRP009 Peripartum Cardiomyopathy 55 2.334
490
c MJR008 Major Affective Disorder 2 34 2.330
491
LWC001 Low Compliance Bladder 45 2.322
492
INT007 Intermediate Coronary Syndrome 54 2.321
493
OST012 Osteoarthritis 77 2.319
494
P MTR003 Mitral Valve Stenosis 53 2.317
495
EMP001 Empty Sella Syndrome 42 2.306
496
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 2.302
497
c SYS001 Systemic Lupus Erythematosus 87 2.288
498
P PLY018 Polycythemia 56 2.288
499
ART016 Aortic Aneurysm 68 2.283
500
HMP005 Hemiplegia 54 2.280
501
SDD001 Sudden Infant Death Syndrome 60 2.275
502
P MLG056 Malignant Hyperthermia 66 2.275
503
P ATR010 Atrial Heart Septal Defect 58 2.275
504
PRS030 Persistent Fetal Circulation Syndrome 49 2.275
505
BRN009 Burning Mouth Syndrome 51 2.268
506
P OVR049 Ovarian Disease 52 2.263
507
P ART022 Arthritis 71 2.260
508
P NTR004 Neutropenia 63 2.260
509
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 2.242
510
PLY150 Polykaryocytosis Inducer 29 2.234
511
P GRV001 Graves' Disease 55 2.234
512
P MYC008 Myocarditis 59 2.228
513
ADR041 Adrenal Cortical Adenoma 49 2.225
514
FCL014 Focal Epilepsy 53 2.217
515
P GST053 Gastric Cancer 83 2.214
516
P CNJ013 Conjunctivitis 66 2.212
517
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 2.210
518
P ANG001 Angelman Syndrome 65 2.208
519
P GCH001 Gaucher's Disease 70 2.208
520
LYM017 Lyme Disease 62 2.203
521
PLM033 Pulmonary Embolism 58 2.203
522
c ACT249 Acute Asthma 40 2.200
523
P BCL017 B-Cell Lymphoma 59 2.200
524
TTR005 Tetrahydrobiopterin Deficiency 48 2.200
525
c SVR005 Severe Pre-Eclampsia 50 2.199
526
SPC005 Speech Disorder 45 2.180
527
DSS009 Disseminated Intravascular Coagulation 57 2.178
528
P EYD002 Eye Disease 57 2.175
529
PCK003 Pick Disease of Brain 69 2.175
530
c RST012 Restless Legs Syndrome 1 33 2.174
531
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.172
532
P TTR001 Tetralogy of Fallot 69 2.172
533
PRD002 Periodic Limb Movement Disorder 34 2.172
534
P VSC011 Vasculitis 61 2.172
535
P PNC035 Pancreatic Cancer 86 2.171
536
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.171
537
PRX097 Paroxysmal Dystonia 32 2.171
538
c THY107 Thymoma, Familial 42 2.163
539
P THY023 Thymoma 64 2.163
540
P LPS004 Lupus Erythematosus 61 2.157
541
PRP016 Paraplegia 52 2.152
542
PPL001 Papillary Adenoma 44 2.150
543
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.148
544
c SCH085 Schizophrenia 2 27 2.143
545
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 2.143
546
ETH004 Euthyroid Sick Syndrome 38 2.142
547
P OPT006 Optic Nerve Disease 58 2.139
548
ESP021 Esophageal Cancer 83 2.138
549
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 2.131
550
P MTC069 Mitochondrial Disorders 57 2.120
551
c HRD173 Hereditary Late-Onset Parkinson Disease 49 2.108
552
P TRN020 Turner Syndrome 67 2.108
553
P HYP730 Hypogonadotropic Hypogonadism 53 2.108
554
PRT013 Portal Hypertension 59 2.108
555
RTR011 Retroperitoneal Fibrosis 47 2.108
556
c BCT007 Bacterial Meningitis 55 2.101
557
P MNN013 Meningitis 65 2.101
558
CVD001 Covid-19 57 2.096
559
MTC005 Mitochondrial Metabolism Disease 45 2.095
560
BRN045 Brunner Syndrome 52 2.081
561
CHR682 Chronic Bilirubin Encephalopathy 37 2.071
562
PRP027 Peripheral Vascular Disease 71 2.050
563
KRN002 Kearns-Sayre Syndrome 63 2.050
564
P HML002 Hemolytic Anemia 62 2.050
565
ATY001 Atypical Depressive Disorder 45 2.049
566
P ACT010 Acth-Secreting Pituitary Adenoma 61 2.049
567
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 2.041
568
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 58 2.039
569
P GST044 Gastritis 55 2.036
570
P DYS005 Dyslexia 41 2.027
571
LTN004 Late-Onset Retinal Degeneration 60 2.021
572
HYP722 Hyperphenylalaninemia, Mild, Non-Bh4-Deficient 23 2.019
573
c ORT012 Orthostatic Hypotension 2 20 2.019
574
c MLT156 Multiple Endocrine Neoplasia, Type I 72 2.018
575
VRC005 Varicose Veins 60 2.015
576
P ATX030 Ataxia-Telangiectasia 80 2.012
577
THY111 Thyroid Carcinoma, Familial Medullary 67 2.012
578
THY125 Thyroid Gland Medullary Carcinoma 48 2.012
579
TLN003 Telangiectasis 51 2.012
580
CRB036 Cerebral Meningioma 35 2.009
582
YLL002 Yellow Fever 61 2.006
583
PCD001 Pica Disease 38 2.006
584
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 60 1.999
585
c SCH052 Schizophrenia 14 19 1.986
586
P SHR121 Short Sleep, Familial Natural, 1 18 1.986
587
P PRN023 Prion Disease 60 1.986
588
DPR002 Depersonalization Disorder 41 1.986
589
P CRD246 Cardiovascular System Disease 56 1.984
590
HYP264 Hypertonia 36 1.983
591
ATH004 Athetosis 25 1.983
592
c NRB010 Neuroblastoma 1 59 1.982
593
P OVR042 Ovarian Cancer 88 1.979
594
TRT001 Teratocarcinoma 42 1.970
595
PNK001 Pink1 Type of Young-Onset Parkinson Disease 8 1.970
596
CHR178 Chromosomal Triplication 34 1.970
597
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.966
598
P ESP024 Esophagitis 60 1.963
599
STN005 St Anthony's Fire 18 1.960
600
c HYP836 Hypercholesterolemia, Familial, 1 73 1.953
601
P MYP004 Myopathy 67 1.953
602
P PRD006 Prader-Willi Syndrome 61 1.953
603
P ART018 Aortic Valve Insufficiency 52 1.953
604
GNG008 Ganglioneuroblastoma 47 1.953
605
GTR002 Goiter 53 1.953
606
c PRG018 Paragangliomas 1 59 1.952
607
BLP048 Blepharospasm, Benign Essential 37 1.933
608
HYP085 Hypothalamic Disease 38 1.933
609
DYS192 Dystonia, Dopa-Responsive 55 1.922
610
c ATM075 Autoimmune Encephalitis 40 1.922
611
c THR092 Thrombophilia Due to Thrombin Defect 74 1.919
612
P MST009 Mastocytosis 64 1.919
613
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.918
614
PRC013 Pericarditis 53 1.918
615
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.915
616
P SCK005 Sickle Cell Disease 56 1.904
617
ANR040 Aneurysm 61 1.895
618
c SCH080 Schizophrenia 3 28 1.895
619
c DMN005 Diamond-Blackfan Anemia 2 28 1.895
620
RTN003 Retinal Ischemia 49 1.895
621
PLG002 Plague 58 1.895
623
KLP001 Kleptomania 36 1.890
624
P BRB001 Beriberi 44 1.884
625
CHL068 Cholestasis 61 1.884
626
CRN036 Craniopharyngioma 64 1.873
627
P THY032 Thyroiditis 57 1.861
629
MCR379 Microcystic Stromal Tumor 29 1.856
630
CLT003 Colitis 63 1.848
631
PRS021 Prostatic Adenoma 43 1.848
632
PRS045 Prostatic Hypertrophy 53 1.848
633
MYC005 Myocardial Stunning 46 1.848
634
CLR030 Clear Cell Renal Cell Carcinoma 54 1.847
635
AGR002 Agoraphobia 45 1.843
636
P EPL198 Epilepsy, Myoclonic Juvenile 61 1.831
637
HYP017 Hypophosphatemia 49 1.827
638
SPS003 Spastic Diplegia 53 1.822
639
TRC010 Trichotillomania 50 1.820
640
c INH030 Inherited Retinal Disorder 28 1.816
641
FND002 Fundus Dystrophy 55 1.816
642
ABT001 Abetalipoproteinemia 68 1.811
643
P INT068 Intestinal Disease 53 1.809
644
DST006 Diastolic Heart Failure 45 1.799
645
ISL135 Isolated Dystonia 22 1.794
646
c GRV008 Graves Disease 1 54 1.794
647
LCH001 Leech Infestation 38 1.794
648
ABD010 Abdominal Wall Defect 39 1.793
649
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.792
650
SMT006 Somatoform Disorder 50 1.786
651
P EPL140 Epilepsy, Idiopathic Generalized 62 1.782
652
ADR008 Adrenal Adenoma 55 1.781
653
P SNS001 Sensorineural Hearing Loss 59 1.774
654
CHL065 Cholangiocarcinoma 58 1.773
655
AKN002 Akinetic Mutism 36 1.773
656
INT079 Intrahepatic Cholangiocarcinoma 51 1.773
657
P PRC019 Precocious Puberty 47 1.760
658
LNG099 Lung Disease 62 1.759
659
c SPN309 Spinocerebellar Ataxia 6 58 1.754
660
MTN003 Motion Sickness 51 1.741
661
P ART023 Arthropathy 61 1.740
662
PTT003 Pituitary-Dependent Cushing's Disease 39 1.740
663
P DYS193 Dystonia 11, Myoclonic 55 1.740
664
QDR001 Quadriplegia 50 1.740
665
PRS129 Prostatic Hyperplasia, Benign 49 1.734
666
NRG002 Neurogenic Bladder 55 1.734
667
CCN009 Cocaine Intoxication 30 1.730
669
VCC001 Vaccinia 47 1.730
670
OCL066 Oculogyric Crisis 35 1.725
671
DSS032 Disease by Infectious Agent 55 1.725
672
GT001 Gout 64 1.725
673
P HYP061 Hypertrophic Cardiomyopathy 69 1.725
674
P ART021 Arteriosclerosis 54 1.725
675
ADN027 Adenomyosis 57 1.717
676
P INF038 Influenza 68 1.717
677
P MLN007 Male Infertility 56 1.704
678
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.703
679
CYS001 Cystic Fibrosis 78 1.694
680
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.694
681
P SCL018 Scoliosis 57 1.694
682
CHR074 Choriocarcinoma 46 1.694
683
P SHR001 Short Bowel Syndrome 53 1.694
684
DYT003 Dyt-Gnal 16 1.694
685
BNS003 Binswanger's Disease 41 1.694
686
P ANR048 Aniridia 1 64 1.692
687
P DRM053 Dermatitis, Atopic 65 1.689
688
c PRG011 Progressive Myoclonus Epilepsy 41 1.684
689
P HMN010 Hemangioma 62 1.684
690
DMP001 Dumping Syndrome 43 1.684
691
GST050 Gastrointestinal System Disease 55 1.684
692
P MYC026 Myoclonus Epilepsy 35 1.684
693
BRN024 Bronchitis 67 1.652
694
BRK012 Broken Heart Syndrome 42 1.652
695
GST045 Gastroenteritis 58 1.638
696
MDD018 Middle East Respiratory Syndrome 44 1.637
697
DSS002 Dissociative Amnesia 28 1.637
698
P URN019 Urinary Tract Infection 49 1.628
699
P AST005 Asthma 76 1.627
700
P SML001 Small Cell Carcinoma 52 1.624
701
c LKM061 Leukemia, Acute Myeloid 83 1.624
702
c NRF024 Neurofibromatosis, Type I 72 1.624
703
PLM022 Pulmonary Valve Insufficiency 45 1.624
704
P LNG028 Long Qt Syndrome 64 1.624
705
ATH013 Atherosclerosis Susceptibility 63 1.615
706
P OCL001 Ocular Albinism 48 1.615
707
LMB062 Limb Ischemia 55 1.615
709
OVR063 Overnutrition 42 1.615
710
RHM001 Rheumatic Fever 59 1.615
711
CRT072 Creutzfeldt-Jakob Disease 68 1.608
712
c DYS151 Dystonia 25 40 1.608
713
P ALP008 Alopecia 54 1.608
714
PLC005 Placental Insufficiency 56 1.608
715
P CMP008 Compartment Syndrome 50 1.608
716
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 1.595
717
VRL011 Viral Infectious Disease 61 1.595
718
END057 Endometrial Cancer 72 1.587
719
c SCH082 Schizophrenia 5 23 1.587
720
ULC004 Ulcerative Colitis 74 1.587
721
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.587
722
P HYP750 Hypertriglyceridemia, Familial 62 1.575
723
RNL077 Renal Fibrosis 46 1.575
724
MCP006 Mucoepidermoid Carcinoma 48 1.575
725
P TBR001 Tuberous Sclerosis 69 1.575
726
PST048 Postural Orthostatic Tachycardia Syndrome 46 1.575
727
KFR001 Kufor-Rakeb Syndrome 59 1.563
728
HYD002 Hydronephrosis 58 1.563
729
RYN005 Raynaud Phenomenon 45 1.563
730
c RNG015 Ring Chromosome 2 22 1.563
731
SPC010 Speech and Communication Disorders 48 1.558
732
P STR020 Strabismus 56 1.558
733
MCH006 Mechanical Strabismus 40 1.558
734
RSP007 Respiratory Distress Syndrome, Infant 40 1.558
735
VLC001 Velocardiofacial Syndrome 57 1.551
736
RHB024 Rhabdomyosarcoma 2 67 1.541
737
c WLF013 Wolfram Syndrome 1 60 1.535
738
PRX035 Paroxysmal Dyskinesia 30 1.535
739
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.535
740
c OPT053 Optic Atrophy 1 62 1.535
741
P ANP001 Anaplastic Large Cell Lymphoma 61 1.535
742
PRP080 Peripheral Artery Disease 54 1.535
743
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 1.535
744
PRP015 Paraphilia Disorder 31 1.535
745
P MSC003 Muscular Atrophy 52 1.535
746
P CHL066 Cholangitis 52 1.535
747
P PLM036 Pulmonary Fibrosis 66 1.535
748
P ACN011 Acne 57 1.535
749
CRD001 Cardiac Tamponade 43 1.535
750
NPH010 Nephrosclerosis 50 1.535
751
P FML018 Familial Mediterranean Fever 73 1.535
752
P MDL005 Medulloblastoma 75 1.535
753
BRC012 Brucellosis 66 1.535
754
FRG010 Fragile X Tremor/ataxia Syndrome 44 1.534
756
PHR003 Pharyngitis 58 1.531
757
PRT019 Protein-Losing Enteropathy 45 1.528
758
c MCL013 Mucolipidosis Iv 65 1.528
759
KRT002 Keratomalacia 55 1.524
760
CLS049 Classic Phenylketonuria 41 1.516
761
THR024 Thrombosis 56 1.516
762
c PRG020 Paragangliomas 3 39 1.516
763
URT049 Urate Oxidase, Pseudogene 24 1.516
764
TLG001 Telogen Effluvium 31 1.516
765
AML001 Amelanotic Melanoma 37 1.516
766
PTT008 Pituitary Carcinoma 46 1.508
767
CRD132 Cardiac Conduction Defect 60 1.507
768
INS001 Insulinoma 59 1.507
769
P MYS003 Myasthenia Gravis 68 1.493
770
MSC007 Muscle Hypertrophy 64 1.493
771
EWN003 Ewing Sarcoma 70 1.493
772
TRG002 Trigeminal Neuralgia 61 1.493
773
P THR014 Thrombocytopenia 66 1.493
774
NSP002 Nasopharyngitis 45 1.493
775
P NSP012 Nasopharyngeal Carcinoma 61 1.485
776
P MYC084 Mycobacterium Tuberculosis 1 68 1.485
777
CYC001 Cycloplegia 34 1.485
778
P PRD037 Periodontal Ehlers-Danlos Syndrome 49 1.485
779
c ACR088 Aicardi-Goutieres Syndrome 3 39 1.478
780
P ASP001 Asperger Syndrome 48 1.478
781
P HPT021 Hepatitis 69 1.478
782
BDY001 Body Dysmorphic Disorder 41 1.469
784
c PRK100 Parkinson Disease 23, Autosomal Recessive Early-Onset 25 1.466
785
ISL001 Islet Cell Tumor 56 1.466
786
P INT070 Intestinal Obstruction 57 1.460
787
c SPN294 Spinocerebellar Ataxia 1 53 1.455
788
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 1.450
789
DSR074 Disorder of Purine Metabolism 23 1.450
790
CHR005 Chorioamnionitis 50 1.450
791
MLR004 Malaria 80 1.450
792
WST001 West Syndrome 59 1.450
793
BCT021 Bacterial Sepsis 43 1.450
794
HLC007 Helicobacter Pylori Infection 67 1.450
795
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.449
796
MYF002 Myofascial Pain Syndrome 46 1.448
797
P MCR129 Microvascular Complications of Diabetes 1 68 1.447
798
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.446
799
ORM002 Oromandibular Dystonia 40 1.444
800
PRM020 Premenstrual Tension 39 1.444
801
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.439
802
KLN009 Kleine-Levin Hibernation Syndrome 41 1.418
803
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.416
804
CHD004 Chudley-Mccullough Syndrome 48 1.413
805
CRN030 Coronary Stenosis 50 1.413
806
GST033 Gestational Diabetes 61 1.413
807
INT030 Intracranial Aneurysm 55 1.413
808
ILS001 Ileus 50 1.410
809
c SCL052 Scleroderma, Familial Progressive 61 1.410
810
BNR002 Bone Resorption Disease 47 1.410
811
ASP008 Aspiration Pneumonitis 42 1.410
812
BRK010 Burkitt Lymphoma 66 1.404
813
P APL001 Aplastic Anemia 73 1.404
814
ALX002 Alexithymia 37 1.404
815
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.404
816
TST044 Testicular Torsion 45 1.404
817
P FML340 Familial Episodic Pain Syndrome 50 1.404
818
P HYP077 Hypertrichosis 46 1.404
819
FTT001 Fatty Liver Disease 62 1.404
820
DSR031 Disorder of Copper Metabolism 25 1.404
822
P HYP069 Hyperparathyroidism 62 1.404
823
KLV001 Kluver-Bucy Syndrome 34 1.404
824
LYM133 Lymphoma, Hodgkin, Classic 74 1.403
825
HYP781 Hypoascorbemia 52 1.403
826
ALV005 Alveolar Soft Part Sarcoma 61 1.403
827
P MYL006 Myeloid Leukemia 61 1.403
828
P MYT002 Myotonic Dystrophy 51 1.403
829
CLL010 Cellular Ependymoma 57 1.396
830
P BNG030 Benign Ependymoma 51 1.396
831
NRM022 Neurometabolic Disease 24 1.389
832
OCC006 Occipital Horn Syndrome 54 1.389
833
P LYM118 Lymphoma 67 1.380
834
LPT006 Leptin Receptor Deficiency 50 1.380
835
SKN019 Skin Melanoma 71 1.380
836
AMD002 Amed Syndrome, Digenic 37 1.380
837
P CLR023 Colorectal Cancer 100 1.376
838
HYP025 Hyperphosphatemia 48 1.376
839
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.376
840
P LKM002 Leukemia 67 1.376
841
THY030 Thyroid Gland Disease 50 1.375
842
c BLD140 Blood Group, I System 46 1.371
843
MLD017 Mal De Debarquement Syndrome 29 1.371
844
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.363
845
c DRR009 Diarrhea 6 45 1.363
846
P ATR011 Atrial Fibrillation 66 1.357
847
ACH005 Achalasia 55 1.357
848
NRR002 Norrie Disease 61 1.357
849
RTN017 Retinal Detachment 60 1.357
850
P FML023 Familial Hemiplegic Migraine 53 1.357
851
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 39 1.357
852
c MYP018 Myopia 6 27 1.357
853
c PRK085 Parkinson Disease 1, Autosomal Dominant 49 1.357
854
GST019 Gastrointestinal Stromal Tumor 78 1.357
855
SCR011 Scrapie 39 1.357
856
OBS004 Obstructive Hydrocephalus 45 1.357
857
c SCH087 Schizophrenia 18 28 1.357
858
WST005 West Nile Virus 57 1.357
859
LMY002 Leiomyoma 51 1.357
860
HRP009 Herpes Simplex Encephalitis 58 1.357
861
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.342
862
SCH014 Schistosomiasis 56 1.342
863
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 52 1.326
864
c HPT073 Hepatitis C Virus 71 1.320
865
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 1.320
866
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 1.320
867
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.316
868
c ACT068 Acute Cystitis 61 1.315
869
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 1.307
870
CHR100 Chronic Ulcer of Skin 57 1.307
871
FCL049 Focal Hand Dystonia 31 1.307
872
c TBR025 Tuberous Sclerosis 1 84 1.307
873
OCL052 Ocular Dominance 40 1.307
874
P CRN249 Cornea Plana 30 1.307
875
BRN018 Borna Disease 36 1.307
876
c BCT013 Bacterial Pneumonia 48 1.307
877
FCT008 Factitious Disorder 34 1.307
878
P GRF003 Graft-Versus-Host Disease 71 1.307
879
SNS003 Sensory Peripheral Neuropathy 52 1.307
880
KLB003 Klebsiella Pneumonia 50 1.307
881
CHL078 Childhood-Onset Schizophrenia 29 1.307
882
HMD003 Hemidystonia 28 1.306
883
P MCR010 Microcephaly 60 1.306
884
PRS063 Paresthesia 39 1.306
885
GGN002 Gigantism 33 1.306
886
P BLD134 Bladder Cancer 79 1.305
887
c CTR110 Cataract 26, Multiple Types 26 1.305
888
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.305
889
NRN002 Neuronitis 31 1.305
890
c GLL024 Gallbladder Disease 1 52 1.301
891
FML035 Familial Hyperlipidemia 55 1.298
892
NRL016 Neural Tube Defects 81 1.296
893
MLT105 Multiple System Atrophy, Cerebellar Type 25 1.296
894
SYS003 Systolic Heart Failure 49 1.296
895
PTT001 Pituitary Hypoplasia 34 1.280
896
c MJR023 Major Affective Disorder 7 33 1.255
897
c MJR004 Major Affective Disorder 4 28 1.255
898
P STR035 Streptococcal Group a Invasive Disease 24 1.254
899
RNL113 Renal Failure, Progressive, with Hypertension 31 1.254
900
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.254
901
CST001 Costello Syndrome 68 1.254
902
AMN015 Amenorrhea-Galactorrhea Syndrome 21 1.254
903
ORL015 Oral Squamous Cell Carcinoma 43 1.254
904
P WLF004 Wolfram Syndrome 61 1.254
905
HMP027 Hemiparkinsonism-Hemiatrophy Syndrome 21 1.254
906
P RHB003 Rhabdomyosarcoma 66 1.254
907
ECH002 Echolalia 33 1.254
908
VRC001 Varicocele 48 1.254
909
BLR008 Bilirubin Metabolic Disorder 57 1.254
910
RTN020 Retinal Vascular Disease 46 1.254
911
P SCK002 Sick Sinus Syndrome 55 1.254
912
P BNC003 Bone Cancer 58 1.254
913
HYP835 Hypothalamic Obesity 38 1.254
914
SGC002 Sgce Myoclonus-Dystonia 24 1.254
915
MYL069 Myeloma, Multiple 77 1.250
916
APN008 Apnea, Obstructive Sleep 67 1.250
917
TXC002 Toxic Encephalopathy 52 1.240
918
PLM001 Pulmonary Tuberculosis 69 1.240
919
P CTR002 Cataract 60 1.240
920
CHL004 Cholelithiasis 49 1.240
921
ADJ001 Adjustment Disorder 47 1.240
922
PPT001 Peptic Esophagitis 52 1.240
923
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.234
924
ACT011 Acute Contagious Conjunctivitis 42 1.234
925
c DPH024 Diaphragmatic Hernia, Congenital 64 1.231
926
SKN016 Skin Disease 63 1.231
927
ASP004 Asphyxia Neonatorum 50 1.231
928
HYP043 Hyperandrogenism 48 1.231
929
P URT039 Urticaria 58 1.231
930
P UVT001 Uveitis 57 1.230
931
BCT002 Bacterial Vaginosis 53 1.230
932
PPL049 Papillon-Lefevre Syndrome 66 1.229
933
c HPT001 Hepatitis C 62 1.211
934
BNG077 Benign Idiopathic Neonatal Seizures 23 1.198
935
GLM044 Glomerular Disease 35 1.198
936
DYS064 Dystonia 3, Torsion, X-Linked 45 1.198
937
c MJR014 Major Depressive Disorder 2 13 1.198
938
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 1.198
939
P ATR001 Atrioventricular Septal Defect 55 1.198
940
c ART101 Aortic Valve Disease 2 66 1.198
941
c SCH075 Schizophrenia 19 27 1.198
942
c GLC092 Glaucoma, Primary Open Angle 62 1.198
943
BSL009 Basal Ganglia Calcification 45 1.198
944
c PRM316 Primary Congenital Hypothyroidism 32 1.198
945
c ACT076 Acute Myocarditis 47 1.198
946
P FBR017 Fibrosarcoma 56 1.198
947
TRY001 Trypanosomiasis 50 1.198
948
CHG001 Chagas Disease 66 1.198
949
CPG001 Capgras Syndrome 26 1.198
950
ALC005 Alcoholic Pancreatitis 38 1.198
951
STM006 Stomach Disease 47 1.198
952
PRT029 Parathyroid Adenoma 51 1.198
953
CNG021 Congenital Toxoplasmosis 55 1.198