Search results for Dopamine

1642 hits were found for Dopamine

# Family MCID Name MIFTS Score
1
DPM001 Dopamine Beta-Hydroxylase Deficiency 47 7.997
2
P PRK101 Parkinsonism-Dystonia, Infantile, 1 39 5.617
3
c ORT011 Orthostatic Hypotension 1 43 4.067
4
BRN112 Brain Dopamine-Serotonin Vesicular Transport Disease 18 3.259
6
c PRK102 Parkinsonism-Dystonia, Infantile, 2 27 2.328
7
DPM008 Dopamine Beta-Hydroxylase, Plasma, Thermolability of 5 2.308
8
P PRK057 Parkinson Disease, Late-Onset 76 0.472
9
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.467
10
P SCH015 Schizophrenia 75 0.440
11
ALC007 Alcohol Dependence 66 0.345
12
PRT037 Pertussis 65 0.305
13
P TRM003 Tremor 53 0.285
14
P NRB001 Neuroblastoma 71 0.274
15
TRD006 Tardive Dyskinesia 55 0.274
16
HYP020 Hyperprolactinemia 64 0.264
17
P PHC003 Pheochromocytoma 71 0.264
18
P BPL003 Bipolar Disorder 56 0.263
19
ADR040 Adrenal Gland Pheochromocytoma 46 0.263
20
c MJR024 Major Affective Disorder 9 41 0.251
21
c MJR022 Major Affective Disorder 8 38 0.251
22
P DYS154 Dystonia 65 0.247
23
ADN018 Adenoma 58 0.245
24
P MVM001 Movement Disease 61 0.240
25
P HNT016 Huntington Disease 71 0.239
26
CCN002 Cocaine Abuse 48 0.238
27
DPR016 Depression 63 0.231
28
P SBS003 Substance Abuse 54 0.231
29
c HYP595 Hypertension, Essential 84 0.223
30
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.220
31
PTT037 Pituitary Tumors 44 0.212
32
P RST001 Restless Legs Syndrome 54 0.209
33
CNG034 Congestive Heart Failure 70 0.206
34
PSY004 Psychotic Disorder 67 0.203
35
TBC004 Tobacco Addiction 64 0.193
36
MNT002 Mental Depression 57 0.193
37
P MJR001 Major Depressive Disorder 68 0.191
38
P ALC033 Alcohol Use Disorder 58 0.183
39
c ACT071 Acute Kidney Failure 59 0.181
40
CCN001 Cocaine Dependence 48 0.181
41
MDD011 Mood Disorder 62 0.181
42
TXC005 Toxic Shock Syndrome 61 0.180
43
HYP266 Hypoxia 56 0.179
44
P KDN018 Kidney Disease 70 0.178
45
PTH002 Pathological Gambling 48 0.177
46
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.174
47
GLL008 Gilles De La Tourette Syndrome 66 0.165
48
OBS002 Obsessive-Compulsive Disorder 68 0.163
49
DRG003 Drug Dependence 47 0.163
50
MLT157 Multiple System Atrophy 1 70 0.159
51
ALL026 Allergic Hypersensitivity Disease 64 0.159
52
ANX010 Anxiety 72 0.158
53
P PTT006 Pituitary Adenoma 54 0.157
54
48X005 48,xyyy 39 0.154
55
P HRT032 Heart Disease 75 0.152
56
PRT058 Pure Autonomic Failure 59 0.152
57
c MGR028 Migraine with or Without Aura 1 69 0.151
58
WTH001 Withdrawal Disorder 48 0.150
59
TRM010 Traumatic Brain Injury 53 0.148
60
P ALZ034 Alzheimer Disease 88 0.142
61
ETN001 Eating Disorder 59 0.142
62
HLX001 Helix Syndrome 47 0.142
63
BRN071 Brain Injury 49 0.140
64
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.140
65
CHR073 Choreatic Disease 52 0.139
66
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.139
67
ACR007 Acromegaly 71 0.138
68
PNG002 Pain Agnosia 51 0.138
69
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.136
70
P ATS364 Autism 65 0.136
71
CHL014 Cholera 55 0.136
72
CRD137 Cardiogenic Shock 48 0.136
73
P SZR006 Seizure Disorder 58 0.135
74
P DMN002 Dementia 67 0.134
75
HYP056 Hypoglycemia 66 0.134
76
c ESS001 Essential Tremor 56 0.134
77
VSL002 Visual Epilepsy 58 0.133
78
PPL052 Papillomatosis, Confluent and Reticulated 34 0.131
79
P PRS038 Personality Disorder 65 0.130
80
P ENC018 Encephalopathy 61 0.130
81
OPD006 Opioid Addiction 48 0.130
82
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.129
83
P MYP006 Myopia 55 0.128
84
P TCD001 Tic Disorder 54 0.125
85
c ATS007 Autism Spectrum Disorder 67 0.122
86
ISC004 Ischemia 60 0.121
87
PST028 Post-Traumatic Stress Disorder 58 0.120
88
OPT003 Opiate Dependence 50 0.120
89
ANR007 Anorexia Nervosa 63 0.118
90
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.117
91
P MJR007 Major Affective Disorder 1 43 0.117
92
P HYP086 Hypothyroidism 68 0.114
93
AGN016 Aging 56 0.114
94
P NRC002 Narcolepsy 51 0.114
95
AMN003 Amnestic Disorder 54 0.113
96
HRT012 Heart Valve Disease 53 0.113
97
SCH012 Schizoaffective Disorder 50 0.113
98
ACT084 Acute Stress Disorder 48 0.113
99
P SLP005 Sleep Disorder 59 0.110
100
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.110
101
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.110
102
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.110
103
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.110
104
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.110
105
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.110
106
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.110
107
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.110
108
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.110
109
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.110
110
SBC016 Subacute Delirium 44 0.108
111
P GLM045 Glioma 63 0.105
112
OVR029 Ovarian Hyperstimulation Syndrome 63 0.105
113
IRN002 Iron Metabolism Disease 57 0.105
114
ANX004 Anoxia 42 0.104
115
HPT019 Hepatic Encephalopathy 60 0.102
116
NRL004 Neuroleptic Malignant Syndrome 55 0.102
117
HPT004 Hepatic Coma 43 0.102
118
END040 Endogenous Depression 54 0.101
119
P CHR345 Chronic Pain 50 0.099
120
IMP006 Impulse Control Disorder 45 0.099
121
P PTS002 Ptosis 52 0.097
122
47X002 47,xyy 49 0.097
123
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.097
124
TQP001 Taqi Polymorphism 32 0.097
125
HYP066 Hyperglycemia 61 0.096
126
RRS014 Rare Surgical Neurologic Disease 32 0.096
127
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.094
128
AMN001 Amenorrhea 54 0.094
129
P RSP003 Respiratory Failure 74 0.092
130
HYP060 Hyperinsulinism 54 0.092
131
P DDN001 Duodenal Ulcer 50 0.092
132
SBS004 Substance Dependence 48 0.092
133
PLY068 Polysubstance Abuse 43 0.092
134
PHN003 Phenylketonuria 75 0.090
135
GLL048 Glial Tumor 45 0.090
136
P CRD119 Cardiac Arrest 67 0.088
137
LSC001 Lesch-Nyhan Syndrome 62 0.088
138
FBR047 Fibromyalgia 59 0.088
139
OCL069 Ocular Motor Apraxia 51 0.088
140
P MYC033 Myoclonus 46 0.088
141
LVR012 Liver Cirrhosis 63 0.087
142
CRT033 Corticobasal Degeneration 55 0.087
143
CND002 Conduct Disorder 51 0.087
144
MRP001 Morphine Dependence 41 0.087
145
CRB039 Cerebrovascular Disease 69 0.085
146
c ACT075 Acute Myocardial Infarction 56 0.085
147
IMP005 Impotence 52 0.085
148
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 50 0.085
149
ATN005 Autonomic Dysfunction 47 0.085
150
RMS001 Rem Sleep Behavior Disorder 44 0.085
151
P EPL164 Epilepsy 71 0.083
152
HRN003 Heroin Dependence 44 0.083
153
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.081
154
DMN031 Dementia, Lewy Body 65 0.081
155
TTN003 Tetanus 64 0.081
156
CNS004 Constipation 57 0.081
157
P PLY011 Polycystic Ovary Syndrome 56 0.081
158
SXL003 Sexual Disorder 48 0.081
159
P MGR001 Migraine Without Aura 48 0.081
160
CRB004 Cerebral Artery Occlusion 44 0.081
161
P FML187 Familial Hypertension 37 0.081
162
SPN186 Spinal Cord Injury 60 0.079
163
BLM002 Bulimia Nervosa 57 0.079
164
P HDC001 Headache 57 0.079
165
P NRP001 Neuropathy 56 0.079
166
HYP005 Hypokalemia 55 0.079
167
P MGR003 Migraine with Aura 50 0.079
168
HYP080 Hypogonadism 50 0.079
169
HYP064 Hypogonadotropism 40 0.079
170
STR067 Stroke, Ischemic 80 0.077
171
GLB015 Glioblastoma Multiforme 75 0.077
172
P PLM037 Pulmonary Hypertension 68 0.077
173
c CHR684 Chronic Kidney Disease 66 0.077
174
SCH003 Schizophreniform Disorder 56 0.077
175
P PRG013 Paraganglioma 52 0.077
176
PRN009 Paranoid Schizophrenia 49 0.077
177
OPD001 Opioid Abuse 45 0.077
178
GLC096 Galactorrhea 42 0.077
179
HRW001 Hair Whorl 36 0.077
180
MNG007 Manganese Poisoning 29 0.077
181
P MYC007 Myocardial Infarction 70 0.074
182
DWN001 Down Syndrome 70 0.074
183
P PTN014 Patent Ductus Arteriosus 1 60 0.074
184
P HYP076 Hyperthyroidism 55 0.074
185
PLM010 Pulmonary Edema 55 0.074
186
GLC003 Glucose Intolerance 54 0.074
187
AVD001 Avoidant Personality Disorder 54 0.074
188
c SCH079 Schizophrenia 1 48 0.074
189
CYT002 Cytokine Deficiency 44 0.074
190
PST092 Posttransplant Acute Limbic Encephalitis 29 0.074
191
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.072
192
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.072
193
WLS001 Wilson Disease 70 0.072
194
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.072
195
END030 End Stage Renal Failure 58 0.072
196
P LTR001 Lateral Sclerosis 53 0.072
197
DLS001 Delusional Disorder 48 0.072
198
SCH011 Schizotypal Personality Disorder 39 0.072
199
P SLP006 Sleep Apnea 69 0.070
200
CRB037 Cerebral Palsy 68 0.070
201
ANG054 Angina Pectoris 66 0.070
202
DSS008 Disease of Mental Health 57 0.070
203
NRT001 Neurotic Disorder 52 0.070
204
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.070
205
SYN036 Syncope 45 0.070
206
CRT015 Carotid Artery Occlusion 44 0.070
207
HND015 Hand Skill, Relative 33 0.070
208
INS024 Insulin-Like Growth Factor I 79 0.068
209
SVR004 Severe Combined Immunodeficiency 73 0.068
210
P LVR013 Liver Disease 68 0.068
211
P NRV007 Nervous System Disease 66 0.068
212
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.068
213
P VSC007 Vascular Disease 63 0.068
214
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.068
215
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.068
216
VSC002 Vascular Dementia 57 0.068
217
c SVR001 Severe Acute Respiratory Syndrome 55 0.068
218
GST037 Gastroparesis 53 0.068
219
P RTN016 Retinal Degeneration 53 0.068
220
P PNC025 Panic Disorder 53 0.068
221
c BPL002 Bipolar I Disorder 49 0.068
222
P HYP265 Hypotonia 42 0.068
223
AMP007 Amphetamine Abuse 40 0.068
224
ALL014 Allergic Encephalomyelitis 39 0.068
225
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.068
226
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.065
227
HMN044 Human Immunodeficiency Virus Type 1 71 0.065
228
MLN008 Melanoma 69 0.065
229
P FRG001 Fragile X Syndrome 68 0.065
230
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.065
231
LPD008 Lipid Metabolism Disorder 62 0.065
232
ATM095 Autoimmune Disease 61 0.065
233
P HYP083 Hypopituitarism 53 0.065
234
GST023 Gastric Ulcer 53 0.065
235
HPT014 Hepatorenal Syndrome 50 0.065
236
SCL003 Social Phobia 48 0.065
237
ANT011 Antisocial Personality Disorder 46 0.065
238
RFR003 Refractive Error 44 0.065
239
CNN001 Cannabis Dependence 38 0.065
240
MLT116 Multiple System Atrophy, Parkinsonian Type 31 0.065
241
c ATR087 Atrial Standstill 1 74 0.063
242
P TRN020 Turner Syndrome 65 0.063
243
PRT036 Peritonitis 65 0.063
244
c PRC016 Pre-Eclampsia 63 0.063
245
P CRN300 Coronary Heart Disease 1 63 0.063
246
P END044 Endometriosis 62 0.063
247
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.063
248
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.063
249
c PNS012 Paine Syndrome 61 0.063
250
P PNC044 Pancreatitis 61 0.063
251
P DRR001 Diarrhea 57 0.063
252
BRN004 Brain Edema 55 0.063
253
PTT009 Pituitary Gland Disease 54 0.063
254
c CNT035 Central Nervous System Disease 54 0.063
255
OCL006 Ocular Hypertension 53 0.063
256
P LCT001 Lactic Acidosis 51 0.063
257
P ECL001 Eclampsia 51 0.063
258
ENT011 Enterocolitis 50 0.063
259
MTB004 Metabolic Acidosis 50 0.063
260
ATX019 Ataxia with Vitamin E Deficiency 48 0.063
261
PPL001 Papillary Adenoma 45 0.063
262
P CLR023 Colorectal Cancer 98 0.060
263
P RTT002 Rett Syndrome 80 0.060
264
c DLT002 Dilated Cardiomyopathy 79 0.060
265
IMM167 Immune Deficiency Disease 78 0.060
266
RCK004 Rickets 69 0.060
267
GNR004 Generalized Anxiety Disorder 56 0.060
268
PRN019 Perinatal Necrotizing Enterocolitis 54 0.060
269
INT075 Intracranial Hypertension 53 0.060
270
BRD004 Borderline Personality Disorder 53 0.060
271
P AST007 Astrocytoma 50 0.060
272
BSL008 Basal Ganglia Disease 43 0.060
273
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.060
274
c ERL056 Early-Onset Parkinson's Disease 39 0.060
275
P STR001 Striatonigral Degeneration 38 0.060
276
NVL002 Novelty Seeking Personality Trait 16 0.060
277
LPT014 Leptin Deficiency or Dysfunction 73 0.057
278
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.057
279
P RTN024 Retinoblastoma 72 0.057
280
P MLT020 Multiple Sclerosis 72 0.057
281
c EXD008 Exudative Vitreoretinopathy 1 69 0.057
282
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.057
283
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
284
P DBT009 Diabetes Mellitus 64 0.057
285
KHL003 Kohlschutter-Tonz Syndrome 64 0.057
286
P CRN018 Coronary Artery Anomaly 63 0.057
287
c FNC043 Fanconi Anemia, Complementation Group E 62 0.057
288
TRN015 Transient Cerebral Ischemia 62 0.057
289
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.057
290
RBS001 Rabies 58 0.057
291
P INF032 Infertility 57 0.057
292
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.057
293
NRN004 Neuroendocrine Tumor 55 0.057
294
c FML008 Familial Retinoblastoma 53 0.057
295
c MCR113 Microvascular Complications of Diabetes 3 52 0.057
296
PRV004 Periventricular Leukomalacia 51 0.057
297
P TMP001 Temporal Lobe Epilepsy 50 0.057
298
OPP004 Oppositional Defiant Disorder 49 0.057
299
P RNL015 Renal Hypertension 48 0.057
300
ANV001 Anovulation 47 0.057
301
c MCR120 Microvascular Complications of Diabetes 7 47 0.057
302
CNN002 Cannabis Abuse 44 0.057
303
FCL022 Focal Dystonia 42 0.057
304
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.057
305
c MCR130 Microvascular Complications of Diabetes 6 41 0.057
306
c MCR133 Microvascular Complications of Diabetes 4 41 0.057
307
P DYS021 Dysautonomia 39 0.057
308
ALD013 Aldosterone-Producing Adenoma 38 0.057
309
c RST012 Restless Legs Syndrome 1 34 0.057
310
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.057
311
CHL079 Children's Interstitial Lung Disease 27 0.057
312
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.057
313
P PRM227 Primary Orthostatic Hypotension 25 0.057
314
HGH001 High Pressure Neurological Syndrome 24 0.057
315
DRG016 Drug Induced Dyskinesia 24 0.057
316
P PRS040 Prostate Cancer 97 0.054
317
OST012 Osteoarthritis 78 0.054
318
P RTN008 Retinitis Pigmentosa 77 0.054
319
DFC004 Deficiency Anemia 75 0.054
320
c MNN043 Meningioma, Familial 74 0.054
321
ACR006 Aceruloplasminemia 73 0.054
322
P FRN006 Frontotemporal Dementia 70 0.054
323
P HPT021 Hepatitis 67 0.054
324
P LKM002 Leukemia 66 0.054
325
c CNG006 Congenital Hypothyroidism 65 0.054
326
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.054
327
P ADL010 Adult Respiratory Distress Syndrome 63 0.054
328
PPL049 Papillon-Lefevre Syndrome 63 0.054
329
MNN042 Meningioma, Radiation-Induced 62 0.054
330
CRD223 Cardiac Arrhythmia 60 0.054
331
ACQ007 Acquired Immunodeficiency Syndrome 60 0.054
332
c ACT027 Acute Pancreatitis 59 0.054
333
PPT005 Peptic Ulcer Disease 58 0.054
334
P CRD246 Cardiovascular System Disease 56 0.054
335
P INF037 Inflammatory Bowel Disease 56 0.054
336
P ATN002 Autonomic Nervous System Disease 52 0.054
337
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 51 0.054
338
PST021 Postpartum Depression 50 0.054
339
SPN021 Spinal Meningioma 47 0.054
340
RTN023 Retinitis 46 0.054
341
HDN002 Head Injury 45 0.054
342
SYD002 Sydenham Chorea 44 0.054
343
GRN017 Granulocytopenia 44 0.054
344
PRM003 Premature Ejaculation 44 0.054
345
OBS003 Obsessive-Compulsive Personality Disorder 44 0.054
346
NRR001 Neuroretinitis 43 0.054
347
c FTL006 Fetal Alcohol Spectrum Disorder 42 0.054
348
TRP009 Triple X Syndrome 42 0.054
349
c SCH082 Schizophrenia 5 38 0.054
350
SCR001 Secretory Meningioma 37 0.054
351
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.054
352
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 19 0.054
353
P LNG032 Lung Cancer 97 0.051
354
P GST053 Gastric Cancer 83 0.051
355
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.051
356
CNN003 Conn's Syndrome 79 0.051
357
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.051
358
P CNR004 Cone-Rod Dystrophy 2 71 0.051
359
P OCL013 Oculodentodigital Dysplasia 69 0.051
360
P PNM007 Pneumonia 68 0.051
361
P ATR011 Atrial Fibrillation 66 0.051
362
P HYP098 Hypereosinophilic Syndrome 66 0.051
363
c RHB024 Rhabdomyosarcoma 2 65 0.051
364
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.051
365
P ADN016 Adenocarcinoma 64 0.051
366
DGR001 Digeorge Syndrome 63 0.051
367
P ORT004 Orthostatic Intolerance 63 0.051
368
P NTR004 Neutropenia 63 0.051
369
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.051
370
P ENC004 Encephalitis 61 0.051
371
ERL001 Early Myoclonic Encephalopathy 61 0.051
372
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.051
373
NWB001 Newborn Respiratory Distress Syndrome 58 0.051
374
P EXN002 Exanthem 57 0.051
375
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.051
376
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.051
377
HRT011 Heart Septal Defect 50 0.051
378
LRN003 Learning Disability 49 0.051
379
GYN001 Gynecomastia 49 0.051
380
ATS010 Autosomal Recessive Disease 48 0.051
381
SRT004 Serotonin Syndrome 46 0.051
382
ACT003 Acute Kidney Tubular Necrosis 45 0.051
383
ATN004 Autonomic Neuropathy 44 0.051
384
c CHR056 Chronic Tic Disorder 43 0.051
385
NNF007 Non-Functioning Pituitary Adenoma 42 0.051
386
RST023 Resting Heart Rate, Variation in 41 0.051
387
RTR011 Retroperitoneal Fibrosis 40 0.051
388
c CHR682 Chronic Bilirubin Encephalopathy 38 0.051
389
c SCH080 Schizophrenia 3 37 0.051
390
c MJR008 Major Affective Disorder 2 34 0.051
391
INF021 Infant Gynecomastia 31 0.051
392
ADG002 Audiogenic Seizures 26 0.051
393
P HPT023 Hepatocellular Carcinoma 100 0.048
394
P BRS047 Breast Cancer 96 0.048
395
P RHM011 Rheumatoid Arthritis 80 0.048
396
AST005 Asthma 77 0.048
397
CRH001 Crohn's Disease 74 0.048
398
P OST002 Osteoporosis 73 0.048
399
P ART022 Arthritis 70 0.048
400
P LYM118 Lymphoma 68 0.048
401
P ANG001 Angelman Syndrome 67 0.048
402
OST159 Osteogenic Sarcoma 66 0.048
403
GST092 Gastroesophageal Reflux 65 0.048
404
IRR002 Irritable Bowel Syndrome 63 0.048
405
P MCH002 Machado-Joseph Disease 63 0.048
406
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.048
407
P VNT002 Ventricular Septal Defect 60 0.048
408
DPH001 Diphtheria 60 0.048
409
STT001 Status Epilepticus 59 0.048
410
c HPT016 Hepatitis B 59 0.048
411
PLM033 Pulmonary Embolism 59 0.048
412
P PRV006 Pervasive Developmental Disorder 57 0.048
413
PLG002 Plague 57 0.048
414
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.048
415
P PRP019 Peripheral Nervous System Disease 57 0.048
416
P DYS193 Dystonia 11, Myoclonic 56 0.048
417
P FTL001 Fetal Alcohol Syndrome 55 0.048
418
DBT010 Diabetic Neuropathy 55 0.048
419
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 53 0.048
420
ART140 Arteries, Anomalies of 53 0.048
421
STT041 Stuttering 52 0.048
422
PTH003 Pathologic Nystagmus 51 0.048
423
P TRT010 Teratoma 51 0.048
424
SMT006 Somatoform Disorder 51 0.048
425
SPS003 Spastic Diplegia 50 0.048
426
P OVR082 Overgrowth Syndrome 50 0.048
427
TRC010 Trichotillomania 50 0.048
428
P ASP001 Asperger Syndrome 48 0.048
429
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.048
430
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.048
431
c INH020 Inherited Metabolic Disorder 46 0.048
432
CYN002 Cyanosis, Transient Neonatal 45 0.048
433
AGR002 Agoraphobia 44 0.048
434
c ERL020 Early-Onset Schizophrenia 44 0.048
435
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.048
436
CRB090 Cerebral Hypoxia 43 0.048
437
c PRM038 Primary Agammaglobulinemia 43 0.048
438
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.048
439
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.048
440
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.048
441
GST020 Gastric Antral Vascular Ectasia 41 0.048
442
49X006 49, Xxxxy Syndrome 41 0.048
443
SPS057 Spasticity 41 0.048
444
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 38 0.048
445
HYP141 Hyperphenylalaninemia 38 0.048
446
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.048
447
PSD088 Pseudobulbar Affect 36 0.048
448
c SCH056 Schizophrenia 15 34 0.048
450
c MJR003 Major Affective Disorder 6 33 0.048
451
c MJR006 Major Affective Disorder 5 33 0.048
452
PST103 Postpartum Psychosis 33 0.048
453
CGN007 Cognitive Function 1, Social 28 0.048
454
P PNC035 Pancreatic Cancer 84 0.044
455
END057 Endometrial Cancer 74 0.044
456
c HYP836 Hypercholesterolemia, Familial, 1 72 0.044
457
PRP027 Peripheral Vascular Disease 71 0.044
458
c GCH015 Gaucher Disease, Type I 70 0.044
459
ADL002 Adult Syndrome 69 0.044
460
c FML001 Familial Atrial Fibrillation 66 0.044
461
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.044
462
P LNG028 Long Qt Syndrome 65 0.044
463
c SML038 Small Cell Cancer of the Lung 65 0.044
464
P MTR014 Motor Neuron Disease 64 0.044
465
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.044
466
P GCH001 Gaucher's Disease 64 0.044
467
P ANR048 Aniridia 1 63 0.044
468
c HPT001 Hepatitis C 63 0.044
469
P PSR002 Psoriasis 62 0.044
470
NTR005 Nutritional Deficiency Disease 61 0.044
471
INT002 Intermittent Claudication 61 0.044
472
P KDN017 Kidney Cancer 61 0.044
473
P CTR002 Cataract 60 0.044
474
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 60 0.044
475
P PLY014 Polycystic Kidney Disease 59 0.044
476
P TRC086 Trichohepatoenteric Syndrome 1 59 0.044
477
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.044
478
GST033 Gestational Diabetes 57 0.044
479
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.044
480
P STR020 Strabismus 56 0.044
481
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.044
482
c FML035 Familial Hyperlipidemia 55 0.044
483
P GRV001 Graves' Disease 55 0.044
484
GNG005 Gangliocytoma 55 0.044
485
CRC006 Carcinoid Syndrome 55 0.044
486
INT007 Intermediate Coronary Syndrome 55 0.044
487
JPN002 Japanese Encephalitis 54 0.044
488
FCL014 Focal Epilepsy 54 0.044
489
BRN045 Brunner Syndrome 53 0.044
490
GLS018 Glass Syndrome 53 0.044
491
GNG002 Ganglioneuroma 53 0.044
492
P INT068 Intestinal Disease 52 0.044
493
c SPN294 Spinocerebellar Ataxia 1 52 0.044
494
PST011 Pustulosis of Palm and Sole 52 0.044
495
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.044
496
HYP081 Hypolipoproteinemia 50 0.044
497
TRT020 Tritanopia 50 0.044
498
BRX001 Bruxism 50 0.044
499
P SCK005 Sickle Cell Disease 50 0.044
500
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.044
501
P OPN001 Open-Angle Glaucoma 49 0.044
502
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.044
503
QDR001 Quadriplegia 48 0.044
504
SMT001 Somatization Disorder 48 0.044
505
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.044
506
P TRT019 Torticollis 47 0.044
507
LPT006 Leptin Receptor Deficiency 47 0.044
508
c MTR002 Mitral Valve Insufficiency 47 0.044
509
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.044
510
c MLG068 Malignant Glioma 45 0.044
511
CRV043 Cervical Dystonia 45 0.044
512
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.044
513
P BRB001 Beriberi 44 0.044
514
CHL012 Childhood Disintegrative Disease 44 0.044
515
DWR001 Dwarfism 44 0.044
516
BCK006 Back Pain 42 0.044
517
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.044
518
CLR033 Color Vision Deficiency 41 0.044
519
P DYS005 Dyslexia 40 0.044
520
ADS004 Aids Dementia Complex 40 0.044
521
ANG049 Angioedema Induced by Ace Inhibitors 40 0.044
522
MCH006 Mechanical Strabismus 39 0.044
523
OCL010 Ocular Hypotension 38 0.044
524
c PLY105 Polycystic Ovary Syndrome 1 38 0.044
525
c PRS136 Prostate Cancer, Hereditary, 6 33 0.044
526
c MJR023 Major Affective Disorder 7 33 0.044
527
c PRS130 Prostate Cancer, Hereditary, 8 32 0.044
528
c HRD198 Hereditary Dystonia 31 0.044
529
c MJR004 Major Affective Disorder 4 28 0.044
530
ARG004 Argyria 28 0.044
531
c ORT012 Orthostatic Hypotension 2 27 0.044
532
SDD004 Sudden Arrhythmia Death Syndrome 23 0.044
533
MTR086 Motor Stereotypies 16 0.044
534
ESP021 Esophageal Cancer 90 0.040
535
P OVR042 Ovarian Cancer 89 0.040
536
c LKM061 Leukemia, Acute Myeloid 83 0.040
537
CYS001 Cystic Fibrosis 80 0.040
538
P BLD134 Bladder Cancer 78 0.040
539
P NRF023 Neurofibromatosis, Type Ii 76 0.040
540
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.040
541
BRN028 Brain Cancer 73 0.040
542
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.040
543
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.040
544
P SYS005 Systemic Scleroderma 70 0.040
545
LYM133 Lymphoma, Hodgkin, Classic 69 0.040
546
SKN019 Skin Melanoma 67 0.040
547
CHL065 Cholangiocarcinoma 67 0.040
548
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 0.040
549
c MCR129 Microvascular Complications of Diabetes 1 66 0.040
550
P HYD006 Hydrocephalus 65 0.040
551
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.040
552
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.040
553
APN008 Apnea, Obstructive Sleep 65 0.040
554
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.040
555
c DYS056 Dystonia 12 64 0.040
556
IDP011 Idiopathic Interstitial Pneumonia 63 0.040
557
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.040
558
CLT003 Colitis 62 0.040
559
P EPL140 Epilepsy, Idiopathic Generalized 61 0.040
560
P PLM036 Pulmonary Fibrosis 61 0.040
561
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.040
562
CHR066 Chronic Fatigue Syndrome 61 0.040
563
c BRN108 Branchiootic Syndrome 1 61 0.040
564
LNG099 Lung Disease 61 0.040
565
P MYL006 Myeloid Leukemia 60 0.040
566
ORL011 Oral Cancer 60 0.040
567
P MYC008 Myocarditis 59 0.040
568
THY029 Thyroid Carcinoma 59 0.040
569
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.040
570
CRD132 Cardiac Conduction Defect 59 0.040
571
c SPN301 Spinocerebellar Ataxia 2 59 0.040
572
EYD002 Eye Disease 58 0.040
573
P GLL020 Gallbladder Disease 58 0.040
574
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.040
575
APH002 Aphasia 57 0.040
576
P GLM007 Glomerulonephritis 57 0.040
577
ADN027 Adenomyosis 57 0.040
578
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 56 0.040
579
P ALP008 Alopecia 56 0.040
580
GST050 Gastrointestinal System Disease 56 0.040
581
PRP009 Peripartum Cardiomyopathy 55 0.040
582
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.040
583
P MLT074 Multiple Endocrine Neoplasia 55 0.040
584
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 0.040
585
IMM102 Immunodeficiency 14 53 0.040
586
c LTN004 Late-Onset Retinal Degeneration 52 0.040
587
ESP023 Esophageal Disease 52 0.040
588
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.040
589
P OLV001 Olivopontocerebellar Atrophy 52 0.040
590
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 51 0.040
591
PPT001 Peptic Esophagitis 51 0.040
592
THY030 Thyroid Gland Disease 51 0.040
593
P MTR003 Mitral Valve Stenosis 50 0.040
594
DYS073 Dysphagia 50 0.040
595
INT079 Intrahepatic Cholangiocarcinoma 50 0.040
596
AMB002 Amblyopia 50 0.040
597
c ACH020 Achromatopsia 2 50 0.040
598
BRN009 Burning Mouth Syndrome 49 0.040
599
c SVR005 Severe Pre-Eclampsia 49 0.040
600
BHR001 Behr Syndrome 49 0.040
601
URM002 Uremia 49 0.040
602
P OBS001 Obstructive Jaundice 48 0.040
603
P CLR019 Color Blindness 48 0.040
604
ASP007 Aspiration Pneumonia 48 0.040
605
IGG001 Iga Glomerulonephritis 48 0.040
606
PLC007 Placental Abruption 48 0.040
607
STM006 Stomach Disease 48 0.040
608
SPC010 Speech and Communication Disorders 47 0.040
609
c LRG017 Large Intestine Cancer 47 0.040
610
HYP082 Hypopharynx Cancer 47 0.040
611
LYM019 Lymphosarcoma 47 0.040
612
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.040
613
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.040
614
CNV002 Conversion Disorder 45 0.040
615
ATY001 Atypical Depressive Disorder 45 0.040
616
IMM064 Immunodeficiency, Common Variable, 10 44 0.040
617
FNC007 Functioning Pituitary Adenoma 44 0.040
618
c HYP272 Hypercholesterolemia, Familial, 3 43 0.040
619
IDP033 Idiopathic Edema 43 0.040
620
P CLS010 Cluster Headache 43 0.040
621
LWC001 Low Compliance Bladder 42 0.040
622
PHY002 Physical Disorder 42 0.040
623
RDN001 Reading Disorder 40 0.040
624
JWD001 Jawad Syndrome 40 0.040
625
MLN003 Melancholia 39 0.040
626
SPP007 Suppression Amblyopia 39 0.040
627
DSS010 Dissociative Disorder 38 0.040
628
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.040
629
FBR089 Fibrosclerosis, Multifocal 38 0.040
630
PLC009 Placenta Praevia 37 0.040
631
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.040
632
CHR178 Chromosomal Triplication 35 0.040
633
CRB036 Cerebral Meningioma 34 0.040
634
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.040
635
c SCH064 Schizophrenia 10 31 0.040
636
MLT105 Multiple System Atrophy, Cerebellar Type 29 0.040
637
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.040
638
GLC025 Galactorrhoea-Hyperprolactinaemia 21 0.040
639
P ATX030 Ataxia-Telangiectasia 83 0.036
640
MLR004 Malaria 80 0.036
641
CRV035 Cervical Cancer 76 0.036
642
MRF001 Marfan Syndrome 75 0.036
643
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.036
644
c NRF024 Neurofibromatosis, Type I 71 0.036
645
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.036
646
P AMY004 Amyloidosis 70 0.036
647
BRN024 Bronchitis 68 0.036
648
P CRN037 Craniosynostosis 68 0.036
649
PCK003 Pick Disease of Brain 68 0.036
650
P MLG056 Malignant Hyperthermia 67 0.036
651
P NSP012 Nasopharyngeal Carcinoma 67 0.036
652
P SKN015 Skin Carcinoma 67 0.036
653
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.036
654
P MSC005 Muscular Dystrophy 66 0.036
655
ATH013 Atherosclerosis Susceptibility 66 0.036
656
P THY023 Thymoma 65 0.036
657
P MYP004 Myopathy 64 0.036
658
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.036
659
SKN016 Skin Disease 63 0.036
660
P NPH012 Nephrotic Syndrome 63 0.036
661
c SCL052 Scleroderma, Familial Progressive 62 0.036
662
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.036
663
P ART023 Arthropathy 62 0.036
664
P HML002 Hemolytic Anemia 62 0.036
665
WLL001 Williams-Beuren Syndrome 62 0.036
666
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.036
667
P VSC011 Vasculitis 62 0.036
668
P ESP024 Esophagitis 62 0.036
669
SDD001 Sudden Infant Death Syndrome 61 0.036
670
VRL011 Viral Infectious Disease 61 0.036
671
RHM001 Rheumatic Fever 61 0.036
672
P ATR010 Atrial Heart Septal Defect 60 0.036
673
ING001 Inguinal Hernia 60 0.036
674
P TXP001 Toxoplasmosis 60 0.036
675
P BNG030 Benign Ependymoma 60 0.036
676
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.036
677
DCB001 Decubitus Ulcer 60 0.036
678
RTN017 Retinal Detachment 60 0.036
679
P SCL018 Scoliosis 60 0.036
680
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.036
681
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.036
682
GST045 Gastroenteritis 59 0.036
683
P INT070 Intestinal Obstruction 58 0.036
684
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.036
685
P OPT006 Optic Nerve Disease 57 0.036
686
LYM027 Lymphopenia 57 0.036
687
TNS005 Tonsillitis 57 0.036
688
HMR039 Hemorrhage, Intracerebral 57 0.036
689
DYS192 Dystonia, Dopa-Responsive 57 0.036
690
THR024 Thrombosis 56 0.036
691
ISL001 Islet Cell Tumor 56 0.036
692
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.036
693
CMM005 Common Cold 56 0.036
694
ADR008 Adrenal Adenoma 56 0.036
695
P GST044 Gastritis 55 0.036
696
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.036
697
ACT058 Active Peptic Ulcer Disease 55 0.036
698
MRD002 Marden-Walker Syndrome 55 0.036
699
P DBT005 Diabetes Insipidus 55 0.036
700
P LYM031 Lymphocytic Leukemia 55 0.036
701
HMP005 Hemiplegia 54 0.036
703
VLC001 Velocardiofacial Syndrome 54 0.036
704
HMS001 Hemosiderosis 54 0.036
705
PRC013 Pericarditis 54 0.036
706
GST009 Gastroschisis 54 0.036
707
c THY107 Thymoma, Familial 54 0.036
708
c LBR014 Leber Congenital Amaurosis 4 53 0.036
709
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.036
710
CLB010 Coloboma of Macula 53 0.036
711
CLL010 Cellular Ependymoma 53 0.036
712
PRP080 Peripheral Artery Disease 53 0.036
713
PRS030 Persistent Fetal Circulation Syndrome 52 0.036
714
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.036
715
P ACT105 Acute Mountain Sickness 52 0.036
716
c GLL024 Gallbladder Disease 1 52 0.036
717
TXC002 Toxic Encephalopathy 52 0.036
718
MTN003 Motion Sickness 52 0.036
719
HYP014 Hyperuricemia 51 0.036
721
TLN003 Telangiectasis 51 0.036
722
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.036
723
HYP781 Hypoascorbemia 50 0.036
724
PNM005 Pneumonic Plague 50 0.036
725
NTR046 Neutrophil Migration 50 0.036
726
P MYT002 Myotonic Dystrophy 49 0.036
727
CHL004 Cholelithiasis 49 0.036
728
c NRC009 Narcolepsy 1 49 0.036
729
SLP001 Sleeping Sickness 48 0.036
730
PLC003 Placental Site Trophoblastic Tumor 48 0.036
731
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 47 0.036
732
WRN003 Wernicke Encephalopathy 47 0.036
733
P CRC039 Coarctation of Aorta 47 0.036
734
c PRK092 Parkinson Disease 6, Autosomal Recessive Early-Onset 47 0.036
735
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.036
736
ANR004 Anuria 46 0.036
737
PRT019 Protein-Losing Enteropathy 46 0.036
738
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.036
739
PST027 Postencephalitic Parkinson Disease 45 0.036
740
c TRC022 Tricuspid Valve Insufficiency 45 0.036
741
IMM003 Immunoglobulin Alpha Deficiency 45 0.036
742
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.036
743
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 45 0.036
744
P BLP003 Blepharospasm 44 0.036
745
DST006 Diastolic Heart Failure 44 0.036
746
P PHR004 Pharynx Cancer 44 0.036
747
EMP001 Empty Sella Syndrome 44 0.036
748
CNT017 Central Nervous System Origin Vertigo 44 0.036
749
DMP001 Dumping Syndrome 44 0.036
750
OVR063 Overnutrition 43 0.036
751
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.036
752
DRG024 Drug Allergy 43 0.036
753
ADR041 Adrenal Cortical Adenoma 43 0.036
754
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 43 0.036
755
c HRD173 Hereditary Late-Onset Parkinson Disease 43 0.036
756
ASP008 Aspiration Pneumonitis 42 0.036
757
c PRG011 Progressive Myoclonus Epilepsy 42 0.036
758
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.036
759
ALX001 Alexia 42 0.036
760
SPC005 Speech Disorder 42 0.036
761
BP1002 Bap1 Tumor Predisposition Syndrome 41 0.036
762
P CRN035 Cranial Nerve Palsy 41 0.036
763
DBT002 Diabetic Autonomic Neuropathy 41 0.036
764
P HYP263 Hypersomnia 41 0.036
765
P RRH023 Rare Hereditary Hemochromatosis 41 0.036
766
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.036
767
BKR002 Baker-Gordon Syndrome 40 0.036
768
c PLM022 Pulmonary Valve Insufficiency 40 0.036
769
PTT003 Pituitary-Dependent Cushing's Disease 39 0.036
770
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.036
771
c MLG157 Malignant Pheochromocytoma 39 0.036
772
ENT001 Enterocele 39 0.036
773
HYP030 Hypoactive Sexual Desire Disorder 39 0.036
774
BLR002 Bile Reflux 39 0.036
775
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.036
776
NNT008 Neonatal Abstinence Syndrome 38 0.036
777
P CRB088 Cerebral Atrophy 38 0.036
778
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.036
779
CHL013 Cholecystolithiasis 37 0.036
780
c PRK085 Parkinson Disease 1, Autosomal Dominant 37 0.036
781
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.036
782
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 36 0.036
783
MYT011 Myotonia 35 0.036
784
ABD010 Abdominal Wall Defect 35 0.036
785
P MYC026 Myoclonus Epilepsy 35 0.036
786
DDN009 Duodenal Obstruction 34 0.036
787
BNN005 Bunion 33 0.036
788
c SCH083 Schizophrenia 7 33 0.036
789
c SCH085 Schizophrenia 2 33 0.036
790
c SCH081 Schizophrenia 6 32 0.036
791
CHR281 Chronic Hiccups 31 0.036
792
MCL057 Macular Dystrophy with Central Cone Involvement 31 0.036
793
CHL078 Childhood-Onset Schizophrenia 31 0.036
794
CLS047 Classic Progressive Supranuclear Palsy Syndrome 30 0.036
795
IDP093 Idiopathic Gastroparesis 30 0.036
796
RSP007 Respiratory Distress Syndrome, Infant 30 0.036
797
PYL002 Pylorospasm 28 0.036
798
PRR019 Perioral Myoclonia with Absences 28 0.036
799
c PRK098 Parkinson Disease 5, Autosomal Dominant 26 0.036
800
FTL073 Fetal Anticonvulsant Syndrome 26 0.036
801
c RST020 Restless Legs Syndrome 6 25 0.036
802
BRR004 Baroreflex Failure 25 0.036
803
JVN026 Jeavons Syndrome 24 0.036
804
DSC013 Discrimination, Two-Point, Reduction in 23 0.036
806
c TYP027 Type 1 Diabetes Mellitus 10 22 0.036
807
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.036
808
CRB089 Cerebral Beriberi 20 0.036
809
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.036
810
FBR090 Fibro-Adipose Vascular Anomaly 17 0.036
811
c SYS001 Systemic Lupus Erythematosus 86 0.031
812
MYL069 Myeloma, Multiple 85 0.031
813
P GLM040 Glioma Susceptibility 1 81 0.031
814
c LKM071 Leukemia, Chronic Lymphocytic 79 0.031
815
P LNG064 Lung Cancer Susceptibility 3 77 0.031
816
P MDL005 Medulloblastoma 77 0.031
817
GST019 Gastrointestinal Stromal Tumor 76 0.031
818
ADR007 Adrenoleukodystrophy 74 0.031
819
ULC004 Ulcerative Colitis 73 0.031
820
SCK003 Sickle Cell Anemia 72 0.031
821
P FML018 Familial Mediterranean Fever 72 0.031
822
MSC157 Muscular Dystrophy, Duchenne Type 71 0.031
823
P SRC025 Sarcoidosis 1 70 0.031
824
PLM001 Pulmonary Tuberculosis 70 0.031
825
P TTR001 Tetralogy of Fallot 69 0.031
826
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.031
827
P LKM062 Leukemia, Acute Lymphoblastic 68 0.031
828
P MYC084 Mycobacterium Tuberculosis 1 68 0.031
829
P INF038 Influenza 68 0.031
830
c INF071 Inflammatory Bowel Disease 1 68 0.031
831
ACR008 Acrocallosal Syndrome 68 0.031
832
P KBK002 Kabuki Syndrome 1 67 0.031
833
P OLG002 Oligodendroglioma 67 0.031
834
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.031
835
THY111 Thyroid Carcinoma, Familial Medullary 67 0.031
836
FLL027 Fallopian Tube Carcinoma 67 0.031
837
P MTR004 Maturity-Onset Diabetes of the Young 66 0.031
838
c LNG044 Long Qt Syndrome 1 66 0.031
839
FCT007 Factor Vii Deficiency 66 0.031
840
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.031
841
c MYT021 Myotonic Dystrophy 1 66 0.031
842
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.031
843
CRN036 Craniopharyngioma 65 0.031
844
MSM014 Mismatch Repair Cancer Syndrome 65 0.031
845
P HRP006 Herpes Simplex 65 0.031
846
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.031
847
c MCL013 Mucolipidosis Iv 64 0.031
848
LYS012 Lysosomal Acid Lipase Deficiency 64 0.031
849
MNK001 Menkes Disease 64 0.031
850
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 0.031
851
NRF007 Neurofibroma 64 0.031
852
PRP083 Porphyria, Acute Intermittent 63 0.031
853
LYM017 Lyme Disease 63 0.031
854
NRM005 Neuromuscular Disease 63 0.031
855
ART002 Arts Syndrome 63 0.031
856
MSC152 Muscular Dystrophy, Becker Type 63 0.031
857
P FRD001 Friedreich Ataxia 63 0.031
858
P PRD008 Periodontitis 62 0.031
859
P HYP055 Hypoplastic Left Heart Syndrome 62 0.031
860
MSS001 Masa Syndrome 62 0.031
861
P PRP029 Porphyria 62 0.031
862
TTH002 Tooth Agenesis 61 0.031
863
P INT143 Interstitial Cystitis 61 0.031
864
P LPS004 Lupus Erythematosus 61 0.031
865
OST003 Osteonecrosis 61 0.031
866
P SNS001 Sensorineural Hearing Loss 61 0.031
867
PRT013 Portal Hypertension 60 0.031
868
P CHL002 Childhood Absence Epilepsy 60 0.031
869
ACN002 Acanthosis Nigricans 60 0.031
870
YLL002 Yellow Fever 60 0.031
871
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.031
872
CYS010 Cystinosis 60 0.031
873
SQM006 Squamous Cell Carcinoma 60 0.031
874
P ALP009 Alopecia Areata 60 0.031
875
INT066 Interstitial Lung Disease 59 0.031
876
GNG013 Gingivitis 59 0.031
877
P SPN309 Spinocerebellar Ataxia 6 59 0.031
878
P BND020 Bone Disease 59 0.031
879
GRD007 Grade Iii Astrocytoma 59 0.031
880
P SYP003 Syphilis 59 0.031
881
CHL123 Chlamydia 59 0.031
882
SPN027 Spinal Stenosis 59 0.031
883
VLV032 Vulva Cancer 59 0.031
884
ANR040 Aneurysm 58 0.031
885
IRN001 Iron Deficiency Anemia 58 0.031
886
c PRG126 Progressive Familial Heart Block 58 0.031
887
ADR005 Adrenal Carcinoma 58 0.031
888
c PRG018 Paragangliomas 1 57 0.031
889
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.031
890
P BNC003 Bone Cancer 57 0.031
891
P EHL001 Ehlers-Danlos Syndrome 57 0.031
892
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.031
893
P SJG008 Sjogren Syndrome 56 0.031
894
PLS011 Plasmacytoma 56 0.031
895
P ORL007 Oral Cavity Cancer 56 0.031
896
P OPT009 Optic Neuritis 56 0.031
897
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.031
898
INT303 Intracranial Hypertension, Idiopathic 56 0.031
899
BCT022 Bacterial Infectious Disease 56 0.031
900
P MLN007 Male Infertility 56 0.031
901
c INT072 Intestinal Pseudo-Obstruction 56 0.031
902
RHM027 Rheumatic Disease 56 0.031
903
VGN017 Vaginal Cancer 55 0.031
904
MCS002 Mucositis 55 0.031
905
BRD001 Brody Myopathy 55 0.031
906
JVN009 Juvenile Pilocytic Astrocytoma 55 0.031
907
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.031
908
LMB002 Lambert-Eaton Myasthenic Syndrome 54 0.031
909
GLS001 Gliosarcoma 54 0.031
910
ORP003 Oropharynx Cancer 54 0.031
911
c PRD040 Periodontitis, Chronic 54 0.031
912
P LRY044 Larynx Cancer 54 0.031
913
UNV001 Unverricht-Lundborg Syndrome 54 0.031
914
LYM040 Lymphoblastic Lymphoma 54 0.031
915
PRT082 Preterm Premature Rupture of the Membranes 54 0.031
916
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.031
917
PRP016 Paraplegia 53 0.031
918
CLR030 Clear Cell Renal Cell Carcinoma 53 0.031
919
MYP139 Myopathy, Proximal, and Ophthalmoplegia 53 0.031
920
NRT004 Neuritis 53 0.031
921
RHM028 Rheumatic Heart Disease 53 0.031
922
SNS003 Sensory Peripheral Neuropathy 53 0.031
923
BRN038 Bronchial Disease 53 0.031
924
P HYP730 Hypogonadotropic Hypogonadism 53 0.031
925
HMC014 Homocysteinemia 53 0.031
926
KRT006 Keratoconjunctivitis 53 0.031
927
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.031
928
KRT009 Keratosis 53 0.031
929
P OVR049 Ovarian Disease 53 0.031
930
THR013 Thoracic Outlet Syndrome 53 0.031
931
CRH005 Crohn's Colitis 52 0.031
932
EXP004 Exophthalmos 52 0.031
933
c DMN023 Diamond-Blackfan Anemia 1 52 0.031
934
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
935
DMY004 Demyelinating Disease 52 0.031
936
P ACT008 Actinic Keratosis 52 0.031
937
GNT002 Giant Cell Glioblastoma 52 0.031
938
c PSR017 Psoriasis 2 52 0.031
939
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.031
940
VSC044 Visceral Myopathy 51 0.031
941
P BRN035 Brain Stem Glioma 51 0.031
942
FND002 Fundus Dystrophy 51 0.031
943
CYS036 Cystinosis, Nephropathic 51 0.031
944
PLS009 Plasma Cell Neoplasm 51 0.031
945
MSC190 Muscular Disease 51 0.031
946
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 0.031
947
SCR020 Sacral Defect with Anterior Meningocele 51 0.031
948
DNT012 Dental Caries 51 0.031
949
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.031
950
APR001 Apraxia 51 0.031
951
PRS021 Prostatic Adenoma 51 0.031
952
THY125 Thyroid Gland Medullary Carcinoma 51 0.031
953
SGW002 Segawa Syndrome, Autosomal Recessive 51 0.031
954
BWN001 Bowen-Conradi Syndrome 51 0.031
955
c ACT134 Acute Liver Failure 51 0.031
956
RTN003 Retinal Ischemia 50 0.031
957
ACH005 Achalasia 50 0.031
958
CHL061 Childhood Leukemia 50 0.031
959
c INF145 Infantile Liver Failure Syndrome 1 50 0.031
960
P ESN008 Eosinophilic Pneumonia 50 0.031
961
HYL004 Hyaline Fibromatosis Syndrome 50 0.031
962
KRT001 Keratoconjunctivitis Sicca 50 0.031
963
c INF023 Inflammatory Breast Carcinoma 49 0.031
964
c PSR023 Psoriasis 1 49 0.031
965
VCC001 Vaccinia 49 0.031
966
LFT001 Left Bundle Branch Hemiblock 49 0.031
967
c DYS119 Dystonia 9 49 0.031
968
P RNV001 Renovascular Hypertension 49 0.031
969
GST049 Gastrointestinal System Cancer 49 0.031
970
ALN001 Aland Island Eye Disease 49 0.031
971
BNR002 Bone Resorption Disease 48 0.031
972
END021 Endomyocardial Fibrosis 48 0.031
973
KRT002 Keratomalacia 48 0.031
974
ENT004 Enthesopathy 48 0.031
975
PLP001 Pulpitis 48 0.031
976
FBR009 Fibrous Dysplasia 48 0.031
977
c DSB006 Desbuquois Dysplasia 1 48 0.031
978
HYP043 Hyperandrogenism 48 0.031
979
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.031
980
c BNG023 Benign Familial Infantile Epilepsy 48 0.031
981
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.031
982
KHN001 Kuhnt-Junius Degeneration 48 0.031
983
P JVN007 Juvenile Absence Epilepsy 48 0.031
984
PLM035 Pulmonary Eosinophilia 48 0.031
985
P NRV006 Nervous System Cancer 48 0.031
986
CRC014 Carcinoid Tumors, Intestinal 48 0.031
987
P UTR058 Uterine Anomalies 48 0.031
988
P PRR002 Pure Red-Cell Aplasia 48 0.031
989
ADR016 Adrenal Cortical Carcinoma 48 0.031
990
P NGH001 Night Blindness 47 0.031
991
DRY001 Dry Eye Syndrome 47 0.031
992
AST006 Astigmatism 47 0.031
993
NRN001 Neuroendocrine Carcinoma 47 0.031
994
SMN008 Semantic Dementia 47 0.031
995
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 47 0.031
996
c INH030 Inherited Retinal Disorder 47 0.031
997
CYC008 Cyclic Vomiting Syndrome 47 0.031
998
HST009 Histiocytoma 46 0.031
999
TTH006 Tooth Disease 46 0.031
1000
c ALP104 Alport Syndrome 3, Autosomal Dominant 46 0.031
1001
c CNT033 Central Nervous System Cancer 46 0.031
1002
ALB002 Albinism 46 0.031
1003
KRT013 Keratolytic Winter Erythema 46 0.031
1004
CNG028 Congenital Hypoplastic Anemia 46 0.031
1005
ANP006 Anaplastic Ependymoma 46 0.031
1006
LCK001 Locked-in Syndrome 46 0.031
1007
TTR005 Tetrahydrobiopterin Deficiency 46 0.031
1008
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 46 0.031
1009
TRT001 Teratocarcinoma 46 0.031
1010
SBP004 Subependymoma 46 0.031
1011
GST071 Gastrointestinal Carcinoma 45 0.031
1012
P EPN001 Ependymoblastoma 45 0.031
1013
MXD026 Mixed Glioma 45 0.031
1014
P OCY003 Oocyte Maturation Defect 1 45 0.031
1015
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.031
1016
MYX001 Myxopapillary Ependymoma 45 0.031
1017
MTS001 Mutism 45 0.031
1018
P END084 Endocrine System Disease 44 0.031
1019
ACT029 Acute Interstitial Pneumonia 44 0.031
1020
CHN010 Chondroma 44 0.031
1021
P GNT008 Giant Cell Tumor 44 0.031
1022
PRT035 Peritoneum Cancer 44 0.031
1023
GNG003 Gingival Recession 44 0.031
1024
P CRB154 Cerebrocostomandibular Syndrome 44 0.031
1025
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.031
1026
MGS001 Megaesophagus 43 0.031
1027
RNL097 Renal Artery Disease 43 0.031
1028
GRW007 Growth Hormone Deficiency 43 0.031
1029
EST005 Esotropia 43 0.031
1030
ACH015 Achalasia, Familial Esophageal 43 0.031
1031
c SRC023 Sarcoidosis 2 43 0.031
1032
CYS009 Cystadenoma 43 0.031
1033
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 43 0.031
1034
MCR011 Microinvasive Gastric Cancer 43 0.031
1035
ANP009 Anaplastic Oligodendroglioma 43 0.031
1036
RDC006 Red Cell Aplasia 42 0.031
1037
AND001 Anodontia 42 0.031
1038
MYF002 Myofascial Pain Syndrome 42 0.031
1039
HYP085 Hypothalamic Disease 42 0.031
1040
EXT022 Exotropia 42 0.031
1041
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 42 0.031
1042
P RNG032 Ring Chromosome 42 0.031
1043
c ADN012 Adenocarcinoma in Situ 42 0.031
1044
DFF003 Diffuse Scleroderma 42 0.031
1045
OCL011 Ocular Motility Disease 41 0.031
1046
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.031
1047
CTN004 Cutaneous Fibrous Histiocytoma 41 0.031
1048
FBR003 Fibrous Histiocytoma 41 0.031
1049
c MLG064 Malignant Ependymoma 41 0.031
1050
ADJ001 Adjustment Disorder 41 0.031
1051
INT319 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked 41 0.031
1052
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 41 0.031
1053
c CNG413 Congenital Short Bowel Syndrome 41 0.031
1054
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.031
1055
CYC005 Cyclothymic Disorder 40 0.031
1056
P NSL008 Nasal Cavity Cancer 40 0.031
1057
PHB003 Phobia, Specific 40 0.031
1058
KLN009 Kleine-Levin Hibernation Syndrome 40 0.031
1059
GLC008 Glucose Metabolism Disease 40 0.031
1060
PRD002 Periodic Limb Movement Disorder 40 0.031
1061
SLT009 Solitary Bone Cyst 40 0.031
1062
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.031
1063
c HMG001 Hemoglobin C Disease 40 0.031
1064
SPR126 Superior Semicircular Canal Dehiscence 40 0.031
1065
ART103 Arthrogryposis, Mental Retardation, and Seizures 40 0.031
1066
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 39 0.031
1067
c EPL133 Epilepsy, Juvenile Absence 1 39 0.031
1068
c PRK093 Parkinson Disease 8, Autosomal Dominant 39 0.031
1069
BDY001 Body Dysmorphic Disorder 39 0.031
1071
ALX002 Alexithymia 39 0.031
1073
c PSR028 Psoriasis 7 39 0.031
1074
NMN001 Nominal Aphasia 39 0.031
1075
c PSR032 Psoriasis 11 38 0.031
1076
c PSR018 Psoriasis 13 38 0.031
1077
c OVR114 Ovarian Cancer 1 38 0.031