Search results for Dopamine

1930 hits were found for Dopamine

# Family MCID Name MIFTS Score
1
DPM001 Dopamine Beta-Hydroxylase Deficiency 47 9.565
2
PRK069 Parkinsonism-Dystonia, Infantile 27 4.418
3
BRN112 Brain Dopamine-Serotonin Vesicular Transport Disease 14 2.560
4
NRN002 Neuronitis 41 0.300
5
P SCH015 Schizophrenia 77 0.292
6
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.186
7
ATN002 Autonomic Nervous System Disease 48 0.146
8
ALC007 Alcohol Dependence 63 0.121
9
DRG011 Drug Addiction 51 0.112
10
P PRK057 Parkinson Disease, Late-Onset 70 0.108
11
P NRB001 Neuroblastoma 70 0.108
12
MVM001 Movement Disease 49 0.108
13
CCN001 Cocaine Dependence 49 0.108
14
CCN002 Cocaine Abuse 48 0.107
15
PRP019 Peripheral Nervous System Disease 55 0.105
16
P DYS154 Dystonia 65 0.104
17
TRD006 Tardive Dyskinesia 49 0.103
18
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.103
19
ADN018 Adenoma 58 0.102
20
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.102
21
P OBS005 Obesity 92 0.101
22
BSL008 Basal Ganglia Disease 40 0.101
23
HYP020 Hyperprolactinemia 60 0.100
24
P BPL003 Bipolar Disorder 62 0.096
25
PTH002 Pathological Gambling 51 0.096
26
P ENC018 Encephalopathy 59 0.095
27
DSS008 Disease of Mental Health 52 0.094
28
SBS003 Substance Abuse 54 0.092
29
CRB009 Cerebritis 39 0.092
30
RST001 Restless Legs Syndrome 54 0.091
31
MDD011 Mood Disorder 61 0.090
32
PTT006 Pituitary Adenoma 56 0.090
33
DRG001 Drug Psychosis 38 0.090
34
OBS002 Obsessive-Compulsive Disorder 66 0.083
35
c PRK031 Parkinson Disease 1 51 0.083
36
DMN002 Dementia 65 0.079
37
c CNT035 Central Nervous System Disease 60 0.079
38
MLT021 Multiple System Atrophy 70 0.077
39
PSY004 Psychotic Disorder 67 0.077
40
PTT037 Pituitary Tumors 45 0.076
41
P ALZ034 Alzheimer Disease 92 0.074
42
P PRS038 Personality Disorder 62 0.074
43
ISC004 Ischemia 61 0.074
44
DRG003 Drug Dependence 50 0.073
45
ANX002 Anxiety Disorder 67 0.071
46
CND002 Conduct Disorder 54 0.071
47
SBS004 Substance Dependence 47 0.071
48
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.071
49
c PRK030 Parkinson Disease 4 38 0.070
50
ETN001 Eating Disorder 58 0.068
51
BRN071 Brain Injury 52 0.068
52
SLP005 Sleep Disorder 53 0.066
53
LRN003 Learning Disability 49 0.066
54
IMP006 Impulse Control Disorder 40 0.066
55
OVR029 Ovarian Hyperstimulation Syndrome 61 0.064
56
PHY002 Physical Disorder 43 0.064
57
P NRV007 Nervous System Disease 71 0.063
58
GLL008 Gilles De La Tourette Syndrome 62 0.063
59
END040 Endogenous Depression 53 0.063
60
HV1006 Hiv-1 80 0.061
61
P PHC003 Pheochromocytoma 71 0.061
62
P TRM003 Tremor 54 0.061
63
MNT002 Mental Depression 53 0.061
64
RTN023 Retinitis 50 0.061
65
PRP027 Peripheral Vascular Disease 68 0.059
66
P EPL164 Epilepsy 66 0.059
67
MTH009 Mouth Disease 61 0.059
68
HYP266 Hypoxia 56 0.059
69
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.059
70
ATN005 Autonomic Dysfunction 49 0.059
71
P HRT032 Heart Disease 75 0.057
72
CNG034 Congestive Heart Failure 72 0.057
73
P ANR007 Anorexia Nervosa 61 0.057
74
VND001 Vein Disease 47 0.057
75
STR067 Stroke, Ischemic 75 0.055
76
PCK002 Pick Disease 68 0.055
77
P HYP086 Hypothyroidism 64 0.055
78
P ALC004 Alcohol Abuse 59 0.055
79
TRM010 Traumatic Brain Injury 52 0.055
80
PRD011 Proud Syndrome 42 0.055
81
HRN003 Heroin Dependence 40 0.055
82
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.055
83
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.055
84
c ALZ040 Alzheimer's Disease 11 27 0.055
85
c CRN175 Coronary Heart Disease 4 19 0.055
86
PRP021 Peripheral Nervous System Neoplasm 46 0.053
87
HPT014 Hepatorenal Syndrome 46 0.053
88
ACR041 Acromelic Frontonasal Dysostosis 45 0.053
89
ALN001 Aland Island Eye Disease 45 0.053
90
P DYS021 Dysautonomia 44 0.053
91
BRT030 Birth Defects 43 0.053
92
c PRK045 Parkinson Disease 5 40 0.053
93
ATN003 Autonomic Nervous System Neoplasm 40 0.053
94
c PRK025 Parkinson Disease 10 38 0.053
95
WTH001 Withdrawal Disorder 37 0.053
96
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.053
97
c PRK051 Parkinson Disease 18 30 0.053
98
c CRN214 Coronary Heart Disease 5 22 0.053
99
c PRK022 Parkinson Disease 12 21 0.053
100
P GLM045 Glioma 60 0.050
101
P NRV006 Nervous System Cancer 60 0.050
102
PST028 Post-Traumatic Stress Disorder 57 0.050
103
BLM002 Bulimia Nervosa 52 0.050
104
P SPS003 Spastic Diplegia 52 0.050
105
PTT009 Pituitary Gland Disease 47 0.050
106
GLT021 Glutaricaciduria, Type I 46 0.050
107
HYP085 Hypothalamic Disease 44 0.050
108
END072 Endotheliitis 42 0.050
109
PHC013 Phaeochromocytoma 41 0.050
110
OBS003 Obsessive-Compulsive Personality Disorder 36 0.050
111
GLB003 Globe Disease 32 0.050
112
c SCH051 Schizophrenia 4 28 0.050
113
c MJR007 Major Affective Disorder 1 24 0.050
114
c MJR008 Major Affective Disorder 2 19 0.050
115
BRN028 Brain Cancer 70 0.048
116
P KDN018 Kidney Disease 66 0.048
117
ACR007 Acromegaly 66 0.048
118
P ATS007 Autism Spectrum Disorder 65 0.048
119
CRB039 Cerebrovascular Disease 63 0.048
120
P NRC002 Narcolepsy 62 0.048
121
LSC001 Lesch-Nyhan Syndrome 61 0.048
122
c ESS001 Essential Tremor 59 0.048
123
EXF001 Exfoliation Syndrome 57 0.048
124
HDC001 Headache 54 0.048
125
RTN018 Retinal Disease 53 0.048
126
ADL002 Adult Syndrome 52 0.048
127
PRT058 Pure Autonomic Failure 52 0.048
128
OPT006 Optic Nerve Disease 52 0.048
129
GNR004 Generalized Anxiety Disorder 51 0.048
130
ATR060 Atrial Standstill, Digenic 51 0.048
131
P CHR345 Chronic Pain 50 0.048
132
OPT003 Opiate Dependence 50 0.048
133
PRN009 Paranoid Schizophrenia 47 0.048
134
P PLN008 Peeling Skin Syndrome 45 0.048
135
HDN002 Head Injury 45 0.048
136
DLS001 Delusional Disorder 41 0.048
137
NRL004 Neuroleptic Malignant Syndrome 41 0.048
138
AYM001 Ayme-Gripp Syndrome 41 0.048
139
ADJ001 Adjustment Disorder 38 0.048
140
SPC003 Specific Developmental Disorder 38 0.048
141
NSY001 N Syndrome 36 0.048
142
NTR005 Nutritional Deficiency Disease 36 0.048
143
FST001 Foster-Kennedy Syndrome 31 0.048
144
c PRK026 Parkinson Disease 11 29 0.048
145
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.048
146
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.048
147
DRG016 Drug Induced Dyskinesia 23 0.048
148
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.046
149
PHN003 Phenylketonuria 72 0.046
150
P HPT021 Hepatitis 69 0.046
151
P END044 Endometriosis 66 0.046
152
P ORT004 Orthostatic Intolerance 64 0.046
153
P SHR029 Short Syndrome 58 0.046
154
MTR014 Motor Neuron Disease 58 0.046
155
BRN004 Brain Edema 52 0.046
156
P MGR003 Migraine with Aura 52 0.046
157
CSY001 C Syndrome 50 0.046
158
NCT008 Nicotine Dependence, Protection Against 49 0.046
159
c PRK059 Parkinson Disease 8 48 0.046
160
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.046
161
MYC033 Myoclonus 42 0.046
162
RMS001 Rem Sleep Behavior Disorder 41 0.046
163
HRT012 Heart Valve Disease 40 0.046
164
c PLN018 Peeling Skin Syndrome 2 40 0.046
165
ADR009 Adrenal Cortex Disease 39 0.046
166
PRP080 Peripheral Artery Disease 37 0.046
167
PST055 Postural Hypotension 36 0.046
168
DVL001 Developmental Coordination Disorder 36 0.046
169
ALR002 Al-Raqad Syndrome 36 0.046
170
SCH011 Schizotypal Personality Disorder 33 0.046
171
c ALZ012 Alzheimer Disease 12 32 0.046
172
c PLN021 Peeling Skin Syndrome 3 29 0.046
173
c CRN174 Coronary Heart Disease 2 20 0.046
174
P GNR027 Generalized Peeling Skin Syndrome 19 0.046
175
c SCH064 Schizophrenia 10 19 0.046
176
c CRN172 Coronary Heart Disease 3 19 0.046
177
c DYS033 Dysautonomia Like Disorder 16 0.046
178
P LNG032 Lung Cancer 95 0.043
179
P HNT016 Huntington Disease 80 0.043
180
c HYP595 Hypertension, Essential 69 0.043
181
P MYP004 Myopathy 67 0.043
182
P INF032 Infertility 59 0.043
183
LPD008 Lipid Metabolism Disorder 58 0.043
184
P HYP060 Hyperinsulinism 58 0.043
185
NRM005 Neuromuscular Disease 56 0.043
186
NRN004 Neuroendocrine Tumor 56 0.043
187
c PND001 Pain Disorder 54 0.043
188
OLV001 Olivopontocerebellar Atrophy 53 0.043
189
BRN106 Burns 52 0.043
190
ALL026 Allergic Hypersensitivity Disease 52 0.043
191
INT007 Intermediate Coronary Syndrome 50 0.043
192
END035 Endocrine Gland Cancer 49 0.043
193
SRT004 Serotonin Syndrome 49 0.043
194
c ACT071 Acute Kidney Failure 49 0.043
195
c INH020 Inherited Metabolic Disorder 49 0.043
196
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.043
197
NSD001 Nose Disease 48 0.043
198
c BPL002 Bipolar I Disorder 47 0.043
199
P CRT033 Corticobasal Degeneration 47 0.043
200
P GNR032 Generalized Dystonia 45 0.043
201
ANV001 Anovulation 44 0.043
202
SXL003 Sexual Disorder 42 0.043
203
FNC007 Functioning Pituitary Adenoma 41 0.043
204
NNF007 Non-Functioning Pituitary Adenoma 41 0.043
205
SPC005 Speech Disorder 41 0.043
206
ADT003 Auditory System Disease 40 0.043
207
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.043
208
HYP070 Hyperpituitarism 38 0.043
209
c PLN017 Peeling Skin Syndrome 1 34 0.043
210
MSC004 Muscle Tissue Disease 34 0.043
211
MRK002 Marek Disease 33 0.043
212
c PRK070 Parkinson Disease 21 27 0.043
213
CRB031 Cerebral Arterial Disease 27 0.043
214
c CRN173 Coronary Heart Disease 8 18 0.043
215
PRM227 Primary Orthostatic Hypotension 18 0.043
216
c MJR004 Major Affective Disorder 4 16 0.043
217
P BRS047 Breast Cancer 100 0.040
218
P OST012 Osteoarthritis 83 0.040
219
P MYC007 Myocardial Infarction 79 0.040
220
GST053 Gastric Cancer 78 0.040
221
P CRN211 Coronary Artery Disease 74 0.040
222
WLS001 Wilson Disease 72 0.040
223
P RSP003 Respiratory Failure 71 0.040
224
P CRD011 Cardiomyopathy 68 0.040
225
SKN016 Skin Disease 66 0.040
226
P PLY011 Polycystic Ovary Syndrome 65 0.040
227
ATS001 Autistic Disorder 63 0.040
228
P ALX003 Alexander Disease 63 0.040
229
P MCH002 Machado-Joseph Disease 63 0.040
230
MLN008 Melanoma 62 0.040
231
RBR001 Roberts Syndrome 60 0.040
232
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.040
233
WLL006 Wells Syndrome 59 0.040
234
RSP006 Respiratory System Disease 58 0.040
235
CHL071 Child Syndrome 58 0.040
236
WST001 West Syndrome 57 0.040
237
P SZR006 Seizure Disorder 56 0.040
238
P MYP006 Myopia 56 0.040
239
HPT019 Hepatic Encephalopathy 56 0.040
240
GLC003 Glucose Intolerance 55 0.040
241
P RTN016 Retinal Degeneration 54 0.040
242
VSC002 Vascular Dementia 54 0.040
243
KDS001 Kid Syndrome 53 0.040
244
P LTR001 Lateral Sclerosis 53 0.040
245
TTH006 Tooth Disease 52 0.040
246
P MSC033 Muscle Disorders 52 0.040
247
LPD004 Lipoid Nephrosis 48 0.040
248
TCD001 Tic Disorder 48 0.040
249
SLP001 Sleeping Sickness 48 0.040
250
BRD004 Borderline Personality Disorder 47 0.040
251
AMN002 Amino Acid Metabolic Disorder 47 0.040
252
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.040
253
INC022 Inclusion-Cell Disease 46 0.040
254
GDS001 Good Syndrome 44 0.040
255
CHR056 Chronic Tic Disorder 44 0.040
256
ANX004 Anoxia 43 0.040
257
MRP001 Morphine Dependence 43 0.040
258
GLC008 Glucose Metabolism Disease 42 0.040
259
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.040
260
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.040
261
BRN080 Brain Ischemia 41 0.040
262
SPC010 Speech and Communication Disorders 41 0.040
263
RPR002 Reproductive System Disease 41 0.040
264
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.040
265
ACT084 Acute Stress Disorder 40 0.040
266
SCH003 Schizophreniform Disorder 40 0.040
267
c ALZ042 Alzheimer's Disease 14 40 0.040
268
SPN369 Spinal Disease 39 0.040
269
CHR073 Choreatic Disease 37 0.040
270
OCL011 Ocular Motility Disease 37 0.040
271
BNS002 Bone Structure Disease 37 0.040
272
c RCR002 Recurrent Hypersomnia 36 0.040
273
FXF002 Fox-Fordyce Disease 36 0.040
274
FCL011 Facial Nerve Disease 36 0.040
275
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.040
276
AMP007 Amphetamine Abuse 35 0.040
277
RDN001 Reading Disorder 34 0.040
278
DPN001 Dependent Personality Disorder 34 0.040
279
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.040
280
c AST037 Asthma 1 28 0.040
281
GNC005 Geniculate Ganglionitis 27 0.040
282
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.040
283
c SCH056 Schizophrenia 15 23 0.040
284
P CRN178 Coronary Heart Disease 6 21 0.040
285
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.040
286
RST012 Restless Legs Syndrome 1 20 0.040
287
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.040
288
GLC025 Galactorrhoea-Hyperprolactinaemia 18 0.040
289
RST014 Restless Legs Syndrome 3 17 0.040
290
EXT011 Extrapyramidal and Movement Disease 13 0.040
291
P CLR023 Colorectal Cancer 97 0.037
292
P AST005 Asthma 82 0.037
293
P LVR013 Liver Disease 75 0.037
294
LVR012 Liver Cirrhosis 67 0.037
295
VSC007 Vascular Disease 67 0.037
296
CRB037 Cerebral Palsy 66 0.037
297
BRC012 Brucellosis 66 0.037
298
DWN001 Down Syndrome 66 0.037
299
CNT098 Central Core Disease 65 0.037
300
P INF037 Inflammatory Bowel Disease 63 0.037
301
APH001 Aphthous Stomatitis 62 0.037
302
P IDP010 Idiopathic Generalized Epilepsy 61 0.037
303
HYP066 Hyperglycemia 61 0.037
304
EYD002 Eye Disease 61 0.037
305
P INT068 Intestinal Disease 60 0.037
306
P PNC025 Panic Disorder 60 0.037
307
P DRR001 Diarrhea 60 0.037
308
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.037
309
GST045 Gastroenteritis 59 0.037
310
P NRP001 Neuropathy 59 0.037
311
ALL006 Allergic Asthma 58 0.037
312
P GT001 Gout 58 0.037
313
ART021 Arteriosclerosis 58 0.037
314
PNC034 Pancreas Disease 58 0.037
315
ABL002 Ablepharon-Macrostomia Syndrome 57 0.037
316
ETH011 Ethylmalonic Encephalopathy 56 0.037
317
ORL011 Oral Cancer 56 0.037
318
TRN015 Transient Cerebral Ischemia 56 0.037
319
P MLT074 Multiple Endocrine Neoplasia 56 0.037
320
PHR003 Pharyngitis 56 0.037
321
GST050 Gastrointestinal System Disease 56 0.037
322
P FNC043 Fanconi Anemia, Complementation Group E 55 0.037
323
P PRG013 Paraganglioma 54 0.037
324
APH002 Aphasia 54 0.037
325
P MCR129 Microvascular Complications of Diabetes 1 54 0.037
326
PLN006 Poland Syndrome 54 0.037
327
P BRN009 Burning Mouth Syndrome 54 0.037
328
HYP080 Hypogonadism 53 0.037
329
P ATX004 Ataxia 53 0.037
330
PTT048 Pituitary Adenoma, Prolactin-Secreting 53 0.037
331
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.037
332
LYM024 Lymphatic System Disease 52 0.037
333
BLD044 Bladder Disease 51 0.037
334
TXC002 Toxic Encephalopathy 51 0.037
335
SPN041 Spinal Cord Disease 51 0.037
336
STM006 Stomach Disease 50 0.037
337
ASP001 Asperger Syndrome 50 0.037
338
URN009 Urinary System Disease 50 0.037
339
OVR063 Overnutrition 50 0.037
340
P URF003 Urofacial Syndrome 1 50 0.037
341
INN002 Inner Ear Disease 49 0.037
342
P INT063 Intellectual Disability 49 0.037
343
FML039 Female Reproductive System Disease 48 0.037
344
P TRC086 Trichohepatoenteric Syndrome 1 48 0.037
345
c HMG001 Hemoglobin C Disease 47 0.037
346
INT253 Intestinal Benign Neoplasm 47 0.037
347
CRB027 Cerebellar Disease 47 0.037
348
MGR028 Migraine with or Without Aura 1 47 0.037
349
UPP004 Upper Respiratory Tract Disease 46 0.037
350
CRB025 Carbohydrate Metabolic Disorder 46 0.037
351
HRT007 Heart Cancer 46 0.037
352
BLD053 Blood Platelet Disease 46 0.037
353
CRB004 Cerebral Artery Occlusion 45 0.037
354
ATN004 Autonomic Neuropathy 45 0.037
355
PTT008 Pituitary Carcinoma 45 0.037
356
ACD009 Acid-Labile Subunit, Deficiency of 45 0.037
357
CRB033 Cerebral Degeneration 44 0.037
358
FCL022 Focal Dystonia 44 0.037
359
CLS010 Cluster Headache 44 0.037
360
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.037
361
BCK006 Back Pain 43 0.037
362
FCT008 Factitious Disorder 41 0.037
363
DCB001 Decubitus Ulcer 41 0.037
364
OPD001 Opioid Abuse 40 0.037
365
GST078 Gastrointestinal Allergy 40 0.037
366
RCT017 Rectal Disease 40 0.037
367
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.037
368
EYL005 Eyelid Disease 39 0.037
369
P HYP265 Hypotonia 38 0.037
370
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 38 0.037
371
CNN001 Cannabis Dependence 38 0.037
372
P UTR038 Uterine Disease 37 0.037
373
BLD054 Blood Protein Disease 37 0.037
374
c CHR579 Chiari Malformation Type Ii 37 0.037
375
P DYS005 Dyslexia 37 0.037
376
c PNC106 Pancreatic Agenesis 1 37 0.037
377
c CNG031 Congenital Nervous System Abnormality 37 0.037
378
c MLT010 Multiple Personality Disorder 36 0.037
379
CRB036 Cerebral Meningioma 36 0.037
380
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.037
381
SYD002 Sydenham Chorea 35 0.037
382
c ALZ032 Alzheimer Disease 18 35 0.037
383
IMP003 Impaired Renal Function Disease 34 0.037
384
MLR007 Male Reproductive System Disease 34 0.037
385
ANG049 Angioedema Induced by Ace Inhibitors 34 0.037
386
PLC008 Placenta Disease 33 0.037
387
SWL001 Swallowing Disorders 33 0.037
388
ATY001 Atypical Depressive Disorder 32 0.037
389
DSS010 Dissociative Disorder 32 0.037
390
P HRT017 Heart Tumor 32 0.037
391
c DRR007 Diarrhea 7 31 0.037
392
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.037
393
c CNT068 Central Pain Syndrome 29 0.037
394
c DRR009 Diarrhea 6 29 0.037
395
c PRK052 Parkinson Disease 17 29 0.037
396
c TRC078 Trichohepatoenteric Syndrome 2 29 0.037
397
c AST039 Asthma 2 28 0.037
398
P STR001 Striatonigral Degeneration 28 0.037
399
TYP027 Type 1 Diabetes Mellitus 10 27 0.037
400
c INF002 Inflammatory Diarrhea 27 0.037
401
c SCH059 Schizophrenia 17 26 0.037
402
YNG002 Young Syndrome 26 0.037
403
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 24 0.037
404
c DYS186 Dystonia 2 22 0.037
405
CRB087 Cerebral Arteriosclerosis 21 0.037
406
c PLY105 Polycystic Ovary Syndrome 1 21 0.037
407
HYP002 Hypothalamic Neoplasm 20 0.037
408
RST020 Restless Legs Syndrome 6 19 0.037
409
c PRK058 Parkinson Disease 16 18 0.037
410
c DYS137 Dystonia 4 18 0.037
411
c CRN176 Coronary Heart Disease 9 18 0.037
412
c ADL079 Adult Heart Tumor 16 0.037
413
RST013 Restless Legs Syndrome 2 16 0.037
414
c SCH061 Schizophrenia 16 16 0.037
415
c MJR003 Major Affective Disorder 6 15 0.037
416
c MJR006 Major Affective Disorder 5 15 0.037
417
INT074 Intracranial Arteriosclerosis 14 0.037
418
P PRS040 Prostate Cancer 90 0.034
419
P RNL014 Renal Cell Carcinoma 82 0.034
420
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.034
421
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.034
422
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.034
423
P MDL005 Medulloblastoma 77 0.034
424
INS024 Insulin-Like Growth Factor I 75 0.034
425
c LKM061 Leukemia, Acute Myeloid 73 0.034
426
c MCL042 Macular Degeneration, Age-Related, 1 73 0.034
427
P INF038 Influenza 72 0.034
428
P PLM036 Pulmonary Fibrosis 71 0.034
429
P LKM002 Leukemia 71 0.034
430
KWS002 Kawasaki Disease 70 0.034
431
P ADN016 Adenocarcinoma 69 0.034
432
P LYM118 Lymphoma 69 0.034
433
ISC006 Ischemic Heart Disease 68 0.034
434
P PNM007 Pneumonia 68 0.034
435
WRN001 Werner Syndrome 67 0.034
436
P MYL005 Myelofibrosis 67 0.034
437
OBS061 Obstructive Sleep Apnea 66 0.034
438
c CHR089 Chronic Kidney Failure 66 0.034
439
P MYL006 Myeloid Leukemia 66 0.034
440
ATP002 Atopy 66 0.034
441
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.034
442
P KDN017 Kidney Cancer 65 0.034
443
P AST007 Astrocytoma 65 0.034
444
DFC004 Deficiency Anemia 64 0.034
445
LNG099 Lung Disease 64 0.034
446
P ENC004 Encephalitis 63 0.034
447
P SLP006 Sleep Apnea 61 0.034
448
P ANG001 Angelman Syndrome 61 0.034
449
CRD119 Cardiac Arrest 61 0.034
450
c ACT075 Acute Myocardial Infarction 60 0.034
451
ACQ007 Acquired Immunodeficiency Syndrome 60 0.034
452
CLT003 Colitis 60 0.034
453
TXC005 Toxic Shock Syndrome 60 0.034
454
P GST049 Gastrointestinal System Cancer 60 0.034
455
PRM097 Primary Immunodeficiency Disease 60 0.034
456
c ACT073 Acute Leukemia 60 0.034
457
WLL001 Williams-Beuren Syndrome 60 0.034
458
GLB001 Gilbert Syndrome 60 0.034
459
P ORL007 Oral Cavity Cancer 59 0.034
460
P NTR004 Neutropenia 59 0.034
461
RHM027 Rheumatic Disease 58 0.034
462
DMN031 Dementia, Lewy Body 58 0.034
463
CTS003 Coats Disease 57 0.034
464
ART017 Aortic Disease 57 0.034
465
CNS004 Constipation 57 0.034
466
c MCR115 Microvascular Complications of Diabetes 5 57 0.034
467
P LYM033 Lymphoproliferative Syndrome 56 0.034
468
P SPN301 Spinocerebellar Ataxia 2 56 0.034
469
P OVR049 Ovarian Disease 56 0.034
470
END030 End Stage Renal Failure 55 0.034
471
MCS002 Mucositis 55 0.034
472
RCT018 Rectal Neoplasm 54 0.034
473
CHN016 Cohen Syndrome 54 0.034
474
GST037 Gastroparesis 54 0.034
475
ESP023 Esophageal Disease 54 0.034
476
NWC001 Newcastle Disease 54 0.034
477
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.034
478
P ECL001 Eclampsia 54 0.034
479
c ART101 Aortic Valve Disease 2 53 0.034
480
C3D001 C3 Deficiency 53 0.034
481
FDL002 Food Allergy 53 0.034
482
P CNT005 Central Nervous System Lymphoma 53 0.034
483
LYM019 Lymphosarcoma 53 0.034
484
PRV006 Pervasive Developmental Disorder 53 0.034
485
PRS042 Prostate Disease 52 0.034
486
P PRM006 Primary Biliary Cirrhosis 51 0.034
487
P LCT001 Lactic Acidosis 51 0.034
488
c INF071 Inflammatory Bowel Disease 1 51 0.034
489
ART002 Arts Syndrome 51 0.034
490
VSC006 Vascular Cancer 51 0.034
491
IMM136 Immune System Disease 51 0.034
492
P CRP007 Carpenter Syndrome 51 0.034
493
CLN019 Colonic Disease 51 0.034
494
c ART115 Aortic Valve Disease 1 50 0.034
495
P HYP065 Hyperaldosteronism 50 0.034
496
SMT006 Somatoform Disorder 50 0.034
497
FML038 Female Reproductive Organ Cancer 50 0.034
498
IMG001 Image Syndrome 50 0.034
499
P CLL015 Collagen Disease 50 0.034
500
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.034
501
ANG054 Angina Pectoris 50 0.034
502
STR081 Stormorken Syndrome 49 0.034
503
LPD009 Lipid Storage Disease 49 0.034
504
c PRM226 Primary Central Nervous System Lymphoma 49 0.034
505
PRN021 Paranasal Sinus Disease 49 0.034
506
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 48 0.034
507
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.034
508
P MYT002 Myotonic Dystrophy 48 0.034
509
MSS002 Mass Syndrome 48 0.034
510
THY030 Thyroid Gland Disease 48 0.034
511
DYS073 Dysphagia 48 0.034
512
RTN020 Retinal Vascular Disease 48 0.034
513
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.034
514
c ERL020 Early-Onset Schizophrenia 47 0.034
515
HYP043 Hyperandrogenism 47 0.034
516
P CRN035 Cranial Nerve Palsy 46 0.034
517
SCL003 Social Phobia 46 0.034
518
CRB090 Cerebral Hypoxia 45 0.034
519
VSC047 Vascular Malformation 45 0.034
520
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 0.034
521
CCN007 Cocoon Syndrome 45 0.034
522
VST004 Vestibular Disease 44 0.034
523
CRD118 Cardiovascular Cancer 44 0.034
524
OCL069 Ocular Motor Apraxia 44 0.034
525
c MTR002 Mitral Valve Insufficiency 44 0.034
526
SKN023 Skin Tag 44 0.034
527
DBT008 Diabetic Angiopathy 44 0.034
528
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.034
529
P SKN013 Skin Benign Neoplasm 43 0.034
530
RNL097 Renal Artery Disease 43 0.034
531
AMN003 Amnestic Disorder 43 0.034
532
SKN027 Skin Conditions 43 0.034
533
MLR006 Male Reproductive Organ Cancer 43 0.034
534
OPP004 Oppositional Defiant Disorder 43 0.034
535
LKC003 Leukocyte Disease 43 0.034
536
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.034
537
P PLM040 Pulmonary Valve Disease 43 0.034
538
PRN019 Perinatal Necrotizing Enterocolitis 42 0.034
539
NRR001 Neuroretinitis 42 0.034
540
P BLD051 Blood Coagulation Disease 42 0.034
541
PRP009 Peripartum Cardiomyopathy 42 0.034
542
APL002 Aplasia of Lacrimal and Salivary Glands 42 0.034
543
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.034
544
c CHR064 Chronic Monocytic Leukemia 42 0.034
545
EGG001 Egg Allergy 41 0.034
546
CNV002 Conversion Disorder 41 0.034
547
CNN002 Cannabis Abuse 40 0.034
548
P PRN020 Paranasal Sinus Cancer 40 0.034
549
PRD002 Periodic Limb Movement Disorder 40 0.034
550
CRN031 Cranial Nerve Disease 40 0.034
551
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.034
552
c INF087 Inflammatory Bowel Disease 4 40 0.034
553
ADS004 Aids Dementia Complex 39 0.034
554
FTT003 Fatty Acid Oxidation Disorders 39 0.034
555
c ADL001 Adult Lymphoma 39 0.034
556
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.034
557
SYN058 Synucleinopathy 38 0.034
558
NSL022 Nasal Cavity Disease 38 0.034
559
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 38 0.034
560
PHS001 Phosphorus Metabolism Disease 38 0.034
561
OCL010 Ocular Hypotension 38 0.034
562
PRL010 Prolactin Producing Pituitary Tumor 38 0.034
563
SXD001 Sex Differentiation Disease 38 0.034
564
PRP028 Peripheral Vertigo 38 0.034
565
c PRS116 Prostate Cancer 1 37 0.034
566
CNT018 Central Nervous System Leukemia 37 0.034
567
MDY003 Mody, Type Ii 36 0.034
568
CPL005 Capillary Disease 36 0.034
569
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.034
570
IMM065 Immunodeficiency 10 36 0.034
571
MTL002 Metal Metabolism Disorder 35 0.034
572
ATS009 Autosomal Genetic Disease 35 0.034
573
PRP026 Peripheral Retinal Degeneration 34 0.034
574
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.034
575
P XLN007 X-Linked Disease 34 0.034
576
c INF089 Inflammatory Bowel Disease 6 34 0.034
577
c MCL040 Macular Degeneration, Age-Related, 3 33 0.034
578
P NSL008 Nasal Cavity Cancer 33 0.034
579
HGH001 High Pressure Neurological Syndrome 33 0.034
580
ACD004 Acdc 33 0.034
581
ALC003 Alcoholic Psychosis 33 0.034
582
P ATS049 Autism Susceptibility, X-Linked 2 33 0.034
583
LYM023 Lymphatic System Cancer 33 0.034
584
MTL005 Metal Allergy 33 0.034
585
P CHR084 Chromosomal Disease 32 0.034
586
c ALZ043 Alzheimer's Disease 15 32 0.034
587
c MCL043 Macular Degeneration, Age-Related, 2 32 0.034
588
CVT001 Cavitary Optic Disc Anomalies 31 0.034
589
c AMY088 Amyotrophic Lateral Sclerosis 3 31 0.034
590
DRG004 Drug-Induced Mental Disorder 31 0.034
591
BLR004 Biliary Dyskinesia 31 0.034
592
P SNS011 Sinus Cancer 31 0.034
593
GST014 Gastrointestinal Lymphoma 31 0.034
594
c HMG004 Hemoglobin D Disease 31 0.034
595
c CRP022 Carpenter Syndrome 2 31 0.034
596
c INF078 Inflammatory Bowel Disease 2 31 0.034
597
c CLR087 Colorectal Cancer 12 30 0.034
598
ACT118 Acute Non Lymphoblastic Leukemia 30 0.034
599
VSC008 Vascular Hemostatic Disease 30 0.034
600
EYD001 Eye Degenerative Disease 30 0.034
601
MRG013 Mirage Syndrome 29 0.034
602
BRW006 Brown Syndrome 29 0.034
603
GRN016 Grant Syndrome 29 0.034
604
c CLR079 Colorectal Cancer 2 29 0.034
605
RDT005 Radiation Induced Cancer 28 0.034
606
c MYC058 Myocardial Infarction 2 28 0.034
607
WRT002 Writing Disorder 27 0.034
608
c PRK037 Parkinson Disease 13 27 0.034
609
RFL002 Reflex Epilepsy 27 0.034
610
PST048 Postural Orthostatic Tachycardia Syndrome 27 0.034
611
c ALZ014 Alzheimer Disease 16 27 0.034
612
c ALZ039 Alzheimer's Disease 7 26 0.034
613
c ANR038 Anorexia Nervosa 1 26 0.034
614
P MCL035 Macular Dystrophy, Retinal, 2 25 0.034
615
ATM052 Autoimmune Disease 1 25 0.034
616
SBC016 Subacute Delirium 24 0.034
617
EYC003 Eye Accommodation Disease 24 0.034
618
CNT017 Central Nervous System Origin Vertigo 24 0.034
619
c ALZ041 Alzheimer's Disease 13 23 0.034
620
SNG003 Single Ventricular Heart 22 0.034
621
c INF091 Inflammatory Bowel Disease 8 22 0.034
622
c NRC011 Narcolepsy 3 22 0.034
623
c ALZ002 Alzheimer Disease Type 1 21 0.034
624
MND006 Mondor Disease 21 0.034
625
SLN005 Silent Pituitary Adenoma 21 0.034
626
c PRK007 Parkinson Disease Type 3 21 0.034
627
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.034
628
c CRN177 Coronary Heart Disease 7 20 0.034
629
c ALZ008 Alzheimer Disease Risk Factor 18 0.034
630
CNT010 Central Nervous System Hematologic Cancer 18 0.034
631
c MLT093 Multiple Sclerosis 2 18 0.034
632
ATN001 Autonomic Peripheral Neuropathy 17 0.034
633
c NRC012 Narcolepsy 4 17 0.034
634
CHR321 Chorea and Dementia 16 0.034
635
ATM053 Autoimmune Disease 2 16 0.034
636
c MCL026 Macular Dystrophy, Retinal, 3 16 0.034
637
RST015 Restless Legs Syndrome 4 14 0.034
638
MGR022 Migraine with or Without Aura 3 14 0.034
639
MGR023 Migraine Without Aura 4 14 0.034
640
WSC001 Wisconsin Syndrome 14 0.034
641
NVD002 Nevada Syndrome 14 0.034
642
RST021 Restless Legs Syndrome 5 14 0.034
643
NVS004 Nova Syndrome 13 0.034
644
c PRN030 Paranasal Sinus Cancer, Adult 12 0.034
645
ORL014 Oral Pharyngeal Disorders 11 0.034
646
TSY001 Tau Syndrome 10 0.034
647
MNT045 Montefiore Syndrome 10 0.034
648
P RHM011 Rheumatoid Arthritis 89 0.030
649
P MLT019 Multiple Myeloma 83 0.030
650
P PLM037 Pulmonary Hypertension 79 0.030
651
P RTT002 Rett Syndrome 77 0.030
652
P OVR042 Ovarian Cancer 76 0.030
653
P ART022 Arthritis 75 0.030
654
CRH001 Crohn's Disease 75 0.030
655
MYL009 Myelodysplastic Syndrome 73 0.030
656
P WSK001 Wiskott-Aldrich Syndrome 73 0.030
657
SCK003 Sickle Cell Anemia 71 0.030
658
TST021 Testicular Germ Cell Tumor 69 0.030
659
c MLT136 Multiple Endocrine Neoplasia 1 69 0.030
660
P FRG001 Fragile X Syndrome 69 0.030
661
P GLB002 Glioblastoma 68 0.030
662
EWN003 Ewing Sarcoma 66 0.030
663
P ATR011 Atrial Fibrillation 66 0.030
664
c BSL007 Basal Cell Carcinoma 65 0.030
665
P HRP006 Herpes Simplex 65 0.030
666
P AMY004 Amyloidosis 65 0.030
667
P PLR004 Pleuropulmonary Blastoma 65 0.030
668
PRT037 Pertussis 64 0.030
669
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.030
670
LYM115 Lymphoma, Non-Hodgkin 63 0.030
671
P CRB042 Cerebellar Ataxia 63 0.030
672
LYM017 Lyme Disease 63 0.030
673
c MYT021 Myotonic Dystrophy 1 63 0.030
674
RNL101 Renal Cell Carcinoma, Papillary 63 0.030
675
PRT036 Peritonitis 63 0.030
676
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.030
677
P MCL013 Mucolipidosis Iv 62 0.030
678
CHR103 Charge Syndrome 62 0.030
679
P LNG064 Lung Cancer Susceptibility 3 62 0.030
680
CNN005 Connective Tissue Disease 62 0.030
681
P VLC001 Velocardiofacial Syndrome 62 0.030
682
GST092 Gastroesophageal Reflux 62 0.030
683
P GCH001 Gaucher's Disease 62 0.030
684
GLC037 Glucocorticoid Resistance 62 0.030
685
HYP056 Hypoglycemia 61 0.030
686
MCK007 Muckle-Wells Syndrome 61 0.030
687
BRS051 Breast Disease 61 0.030
688
P PNC044 Pancreatitis 61 0.030
689
P SNS014 Sinusitis 60 0.030
690
OCL009 Ocular Cancer 59 0.030
691
P GRV001 Graves' Disease 59 0.030
692
P GLL020 Gallbladder Disease 59 0.030
693
c FML001 Familial Atrial Fibrillation 58 0.030
694
BNC003 Bone Cancer 58 0.030
695
ING001 Inguinal Hernia 58 0.030
696
KND001 Kindler Syndrome 57 0.030
697
EMB004 Embryonal Carcinoma 57 0.030
698
ADR005 Adrenal Carcinoma 57 0.030
699
P EXN002 Exanthem 57 0.030
700
ADM013 Adamantinoma of Long Bones 57 0.030
701
SNS001 Sensorineural Hearing Loss 57 0.030
702
P INT070 Intestinal Obstruction 57 0.030
703
HRP004 Herpes Zoster 56 0.030
704
P FRS003 Fraser Syndrome 56 0.030
705
GST023 Gastric Ulcer 56 0.030
706
LYM027 Lymphopenia 56 0.030
707
VRL011 Viral Infectious Disease 55 0.030
708
ART111 Artery Disease 55 0.030
709
P CHL002 Childhood Absence Epilepsy 55 0.030
710
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.030
711
FCL014 Focal Epilepsy 55 0.030
712
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 55 0.030
713
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.030
714
P MMB011 Membranous Nephropathy 54 0.030
715
P THY032 Thyroiditis 54 0.030
716
PLM010 Pulmonary Edema 54 0.030
717
P MTC069 Mitochondrial Disorders 53 0.030
718
DMY004 Demyelinating Disease 53 0.030
719
P HYP024 Hypoparathyroidism 53 0.030
720
c EPL070 Epilepsy, Progressive Myoclonic 2b 53 0.030
721
P DGR001 Digeorge Syndrome 53 0.030
722
c ALZ036 Alzheimer Disease, Type 3 53 0.030
723
LYS002 Lysosomal Storage Disease 52 0.030
724
P ACT105 Acute Mountain Sickness 52 0.030
725
BLR006 Biliary Tract Disease 52 0.030
726
c ALZ037 Alzheimer Disease-2 52 0.030
727
P PTN002 Patent Ductus Arteriosus 52 0.030
728
CRH005 Crohn's Colitis 52 0.030
729
MYC002 Mycobacterium Avium Complex Disease 52 0.030
730
CRC006 Carcinoid Syndrome 52 0.030
731
IMP005 Impotence 51 0.030
732
PHL006 Phelan-Mcdermid Syndrome 51 0.030
733
BRN038 Bronchial Disease 51 0.030
734
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 0.030
735
PLR022 Pleural Disease 51 0.030
736
c SPN309 Spinocerebellar Ataxia 6 51 0.030
737
HYP005 Hypokalemia 51 0.030
738
SCK005 Sickle Cell Disease 51 0.030
739
NTR040 Neutropenia, Cyclic 51 0.030
740
CRN030 Coronary Stenosis 51 0.030
741
DYS014 Dyspepsia 50 0.030
742
BNF002 Bone Fracture 50 0.030
743
HYP006 Hypertensive Heart Disease 50 0.030
744
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.030
745
SPR099 Supravalvar Aortic Stenosis 49 0.030
746
LMB062 Limb Ischemia 48 0.030
747
MTN003 Motion Sickness 48 0.030
748
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 48 0.030
749
P FML035 Familial Hyperlipidemia 48 0.030
750
ADR012 Adrenal Gland Disease 48 0.030
751
CNN003 Conn's Syndrome 48 0.030
752
OCL006 Ocular Hypertension 48 0.030
753
PLS009 Plasma Cell Neoplasm 48 0.030
754
c ATS308 Autosomal Dominant Cerebellar Ataxia 48 0.030
755
MTB004 Metabolic Acidosis 48 0.030
756
CHL004 Cholelithiasis 48 0.030
757
STT041 Stuttering 48 0.030
758
P RNL015 Renal Hypertension 48 0.030
759
PRT030 Parathyroid Gland Disease 47 0.030
760
ANT011 Antisocial Personality Disorder 47 0.030
761
GST009 Gastroschisis 47 0.030
762
SDD007 Sudden Cardiac Death 47 0.030
763
P HRP009 Herpes Simplex Encephalitis 47 0.030
764
SLV003 Salivary Gland Disease 47 0.030
765
BRD001 Brody Myopathy 47 0.030
766
ACH001 Acheiropody 46 0.030
767
P PRM108 Primary Progressive Multiple Sclerosis 46 0.030
768
DST006 Diastolic Heart Failure 46 0.030
769
CRD137 Cardiogenic Shock 46 0.030
770
SNS003 Sensory Peripheral Neuropathy 45 0.030
771
P CRV039 Cervicitis 45 0.030
772
RFR010 Refractory Anemia 45 0.030
773
SPH010 Sphingolipidosis 45 0.030
774
SMN008 Semantic Dementia 44 0.030
775
CRD001 Cardiac Tamponade 44 0.030
776
P BRN120 Bronchus Cancer 44 0.030
777
GRN017 Granulocytopenia 44 0.030
778
PRM020 Premenstrual Tension 44 0.030
779
3MS007 3-M Syndrome 1 43 0.030
780
SYS003 Systolic Heart Failure 43 0.030
781
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.030
782
ACT058 Active Peptic Ulcer Disease 43 0.030
783
SNS023 Sensory System Cancer 43 0.030
784
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.030
785
PRD004 Prediabetes Syndrome 43 0.030
786
P CRD132 Cardiac Conduction Defect 43 0.030
787
MLT001 Multiple Chemical Sensitivity 43 0.030
788
P CRB088 Cerebral Atrophy 42 0.030
789
BHR001 Behr Syndrome 42 0.030
790
SPS057 Spasticity 42 0.030
791
YWS001 Yaws 42 0.030
792
SMT001 Somatization Disorder 42 0.030
793
BLR008 Bilirubin Metabolic Disorder 42 0.030
794
BRN018 Borna Disease 42 0.030
795
DBT002 Diabetic Autonomic Neuropathy 42 0.030
796
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.030
797
VGN020 Vaginal Disease 41 0.030
798
P CPL003 Capillary Leak Syndrome 41 0.030
799
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.030
800
END038 Endocrine Pancreas Disease 41 0.030
801
CLV009 Clove Syndrome, Somatic 41 0.030
802
CRC014 Carcinoid Tumors, Intestinal 40 0.030
803
ENT001 Enterocele 40 0.030
804
P HYP263 Hypersomnia 40 0.030
805
P LBY004 Labyrinthitis 40 0.030
806
PSD029 Pseudocholinesterase Deficiency 40 0.030
807
RTT001 Ritter's Disease 40 0.030
808
DRS004 Door Syndrome 40 0.030
809
ATS008 Autosomal Dominant Disease 39 0.030
810
HYP264 Hypertonia 39 0.030
811
SPN040 Spinal Cancer 39 0.030
812
LYM127 Lymphatic Malformations 39 0.030
813
MYF002 Myofascial Pain Syndrome 39 0.030
814
c ACT004 Acute Diarrhea 39 0.030
815
GND003 Gonadal Disease 39 0.030
816
RTR011 Retroperitoneal Fibrosis 39 0.030
817
ACT088 Acute Insulin Response 39 0.030
818
PGM003 Pigmentation Disease 39 0.030
819
c PRG011 Progressive Myoclonus Epilepsy 39 0.030
820
SCK001 Sick Building Syndrome 38 0.030
821
P FML187 Familial Hypertension 38 0.030
822
ABD010 Abdominal Wall Defect 38 0.030
823
c INF086 Inflammatory Bowel Disease 3 38 0.030
824
GST007 Gastric Dilatation 38 0.030
825
KNZ001 Kanzaki Disease 38 0.030
826
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.030
827
CHL013 Cholecystolithiasis 37 0.030
828
P CNT036 Central Nervous System Germ Cell Tumor 37 0.030
829
FNC002 Functional Diarrhea 37 0.030
830
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.030
831
CLD014 Cole Disease 37 0.030
832
HYP064 Hypogonadotropism 37 0.030
833
STR015 Stereotypic Movement Disorder 36 0.030
834
HRD016 Hereditary Retinal Dystrophy 36 0.030
835
GRM001 Germ Cell and Embryonal Cancer 36 0.030
836
ATM014 Autoimmune Disease of Endocrine System 36 0.030
837
SPN050 Spinocerebellar Degeneration 36 0.030
838
c DYS119 Dystonia 9 36 0.030
839
CHL012 Childhood Disintegrative Disease 35 0.030
840
SBS006 Sebastian Syndrome 35 0.030
841
c PLM022 Pulmonary Valve Insufficiency 34 0.030
842
WRT001 Worth's Syndrome 34 0.030
843
PHB001 Phobic Disorder 34 0.030
844
INT259 Interleukin 1 Receptor Antagonist Deficiency 34 0.030
845
GLS018 Glass Syndrome 34 0.030
846
c GLL024 Gallbladder Disease 1 34 0.030
847
c PRM015 Primary Cerebellar Degeneration 34 0.030
848
MDY004 Mody, Type Iii 34 0.030
849
CRD016 Cardiac Rupture 34 0.030
850
P MYC026 Myoclonus Epilepsy 34 0.030
851
P CRB059 Cerebellar Degeneration 34 0.030
852
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.030
853
DFF002 Diffuse Pulmonary Fibrosis 33 0.030
854
c DGT005 Digital Arthropathy-Brachydactyly, Familial 33 0.030
855
LNS003 Lens Disease 33 0.030
856
SPR024 Supratentorial Cancer 33 0.030
857
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.030
858
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 32 0.030
859
HRM003 Hormone Producing Pituitary Cancer 32 0.030
860
RNL013 Renal Adenoma 32 0.030
861
P ACT080 Acute Pulmonary Heart Disease 31 0.030
862
BLR002 Bile Reflux 31 0.030
863
PRN024 Purine-Pyrimidine Metabolic Disorder 31 0.030
864
c SPN366 Spinocerebellar Ataxia with Axonal Neuropathy Type 2 31 0.030
865
IRS003 Iris Disease 31 0.030
866
MDY005 Mody, Type I 30 0.030
867
c OST147 Osteoarthritis 1 30 0.030
868
TRG003 Trigeminal Nerve Disease 30 0.030
869
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.030
870
c SYS007 Systemic Capillary Leak Syndrome 30 0.030
871
CYL001 Cayler Cardiofacial Syndrome 29 0.030
872
c PRM092 Primary Lateral Sclerosis, Adult, 1 29 0.030
873
c CLR077 Colorectal Cancer 10 29 0.030
874
PYR035 Pyrimidine Metabolic Disorder 29 0.030
875
c NRC009 Narcolepsy 1 29 0.030
876
PRM243 Primary Bone Cancer 29 0.030
877
VSL004 Visual Cortex Disease 28 0.030
878
DYS011 Dyskinesia of Esophagus 28 0.030
879
LPD027 Lip Disease 28 0.030
880
P PTN008 Patent Arterial Duct 27 0.030
881
WDS002 Woods Syndrome 27 0.030
882
c CHR565 Chromosomal Deletion Syndrome 27 0.030
883
ALC013 Alcohol-Induced Mental Disorder 27 0.030
884
CRB018 Cerebral Lipidosis 27 0.030
885
IMM063 Immunodeficiency 15 26 0.030
886
3MS006 3-M Syndrome 3 26 0.030
887
c DYS146 Dystonia 24 26 0.030
888
c WSK002 Wiskott-Aldrich Syndrome 2 25 0.030
889
3MS005 3-M Syndrome 2 25 0.030
890
c ATM007 Autoimmune Disease of Central Nervous System 25 0.030
891
c NRC017 Narcolepsy 7 24 0.030
892
KHL001 Kohler's Disease 24 0.030
893
c MLT094 Multiple Sclerosis 3 24 0.030
894
c MLT124 Multiple Sclerosis 5 23 0.030
895
MLL004 Mallory-Weiss Syndrome 23 0.030
896
PPL023 Pupil Disease 23 0.030
897
c MCR112 Microvascular Complications of Diabetes 2 22 0.030
898
GRM003 German Syndrome 22 0.030
899
INS009 Insulin-Resistance Type B 22 0.030
900
ARG006 Aregenerative Anemia 22 0.030
901
ATM059 Autoimmune Disease 6 22 0.030
902
c GLL027 Gallbladder Disease 4 22 0.030
903
ISC009 Ischemic Retinopathy 21 0.030
904
CMB002 Combat Disorder 21 0.030
905
BRN123 Branchial Arch Syndrome, X-Linked 21 0.030
906
APN006 Apnea of Prematurity 21 0.030
907
c PRK078 Parkinson Disease 22 20 0.030
908
HYP611 Hypoparathyroidism, X-Linked 20 0.030
909
c CHR464 Chronic Intestinal Failure 20 0.030
910
CCN009 Cocaine Intoxication 20 0.030
911
SPN187 Spinocerebellar Atrophy 20 0.030
912
c NRC010 Narcolepsy 2 19 0.030
913
CYT018 Cytochrome P450 2d6 Variant 19 0.030
914
c MNT224 Mental Retardation, X-Linked 101 19 0.030
915
VSC009 Vascular Skin Disease 19 0.030
916
MNT257 Mental Retardation, X-Linked, with Craniofacial Dysmorphism 18 0.030
917
c CHR344 Chronic Orthostatic Intolerance 18 0.030
918
MYT026 Myotonia Atrophica 18 0.030
919
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.030
920
c PTN012 Patent Ductus Arteriosus 3 18 0.030
921
YSY001 Yao Syndrome 17 0.030
922
c ATS170 Autism 19 17 0.030
923
P CNT003 Central Nervous System Embryonal Carcinoma 17 0.030
924
MLL015 Mills Syndrome 17 0.030
925
c NRC013 Narcolepsy 5 17 0.030
926
OLF001 Olfactory Nerve Disease 16 0.030
927
c ATS171 Autism 9 16 0.030
928
c GLL025 Gallbladder Disease 2 16 0.030
929
MXD001 Mixed Cerebral Palsy 16 0.030
930
c GRV009 Graves Disease 2 16 0.030
931
GLC077 Glucocorticoid Therapy, Response to 16 0.030
932
c GLL026 Gallbladder Disease 3 16 0.030
933
c ADL022 Adult Central Nervous System Primitive Neuroectodermal Neoplasm 15 0.030
934
ATM054 Autoimmune Disease 3 15 0.030
935
CDN003 Codeine Toxicity 15 0.030
936
CHR235 Chromosome 22q Deletion 15 0.030
937
ATM055 Autoimmune Disease 4 15 0.030
938
LPN002 Lip and Oral Cavity Cancer 15 0.030
939
c EPL091 Epilepsy, Idiopathic Generalized 3 15 0.030
940
c UTR006 Uterine Inflammatory Disease 15 0.030
941
c PNC068 Panic Disorder 3 15 0.030
942
PRM139 Primary Melanoma of the Central Nervous System 15 0.030
943
MGR024 Migraine with or Without Aura 5 15 0.030
944
HRT029 Heart Tumor of the Child 15 0.030
945
c ATS172 Autism 10 15 0.030
946
c ADL007 Adult Central Nervous System Embryonal Carcinoma 14 0.030
947
DBT003 Diabetic Peripheral Angiopathy 14 0.030
948
c CNT032 Central Nervous System Adult Germ Cell Tumor 14 0.030
949
c PNC070 Panic Disorder 2 14 0.030
950
FNC003 Functionless Pituitary Adenoma 13 0.030
951
MLG045 Malignant Growth Hormone Secreting Neoplasm of Pituitary 13 0.030
952
c EPL092 Epilepsy, Idiopathic Generalized 2 13 0.030
953
c GNR024 Generalized Peeling Skin Syndrome Type C 12 0.030
954
PRS059 Prostaglandin-Endoperoxide Synthase Deficiency 12 0.030
955
INB001 Inborn Amino Acid Metabolism Disorder 12 0.030
956
c EPL090 Epilepsy, Idiopathic Generalized 5 12 0.030
957
ADS006 Aids - Neurological Complications 12 0.030
958
BDS001 Bd Syndrome 12 0.030
959
RST019 Restless Legs Syndrome 8 12 0.030
960
HRD059 Hereditary Peripheral Nervous Disorder 11 0.030
961
MNT033 Mental Retardation X-Linked Dysmorphism 10 0.030
962
ART033 Aortic Valves Stenosis of the Child 9 0.030
963
ATX012 Ataxias and Cerebellar or Spinocerebellar Degeneration 8 0.030
964
P HPT023 Hepatocellular Carcinoma 92 0.026
965
P PNC035 Pancreatic Cancer 87 0.026
966
c SYS001 Systemic Lupus Erythematosus 86 0.026
967
P RTN008 Retinitis Pigmentosa 80 0.026
968
P ATX030 Ataxia-Telangiectasia 77 0.026
969
ESP021 Esophageal Cancer 76 0.026
970
P NRF002 Neurofibromatosis 71 0.026
971
KRT004 Keratitis 71 0.026
972
P LGH007 Leigh Syndrome 70 0.026
973
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.026
974
SQM006 Squamous Cell Carcinoma 70 0.026
975
PLM001 Pulmonary Tuberculosis 67 0.026
976
c NRF018 Neurofibromatosis, Type 1 67 0.026
977
P MNN013 Meningitis 67 0.026
978
P NSP012 Nasopharyngeal Carcinoma 66 0.026
979
URN008 Urinary Bladder Cancer 66 0.026
980
CRV047 Cervical Cancer, Somatic 65 0.026
981
P MSC005 Muscular Dystrophy 65 0.026
982
PTR006 Peters Anomaly 65 0.026
983
CNR002 Cone-Rod Dystrophy 64 0.026
984
P LPS004 Lupus Erythematosus 64 0.026
985
P ART023 Arthropathy 64 0.026
986
P LNG028 Long Qt Syndrome 64 0.026
987
P CNJ013 Conjunctivitis 64 0.026
988
HMT002 Hematologic Cancer 64 0.026
989
c LKM062 Leukemia, Acute Lymphoblastic 64 0.026
990
CHR066 Chronic Fatigue Syndrome 64 0.026
991
P PRP003 Porphyria Cutanea Tarda 64 0.026
992
P OST002 Osteoporosis 64 0.026
993
P HYP098 Hypereosinophilic Syndrome 63 0.026
994
P PRD008 Periodontitis 63 0.026
995
RCT015 Reactive Arthritis 63 0.026
996
GLB015 Glioblastoma Multiforme 63 0.026
997
SPN186 Spinal Cord Injury 63 0.026
998
P FRD001 Friedreich Ataxia 62 0.026
999
LPT001 Leptospirosis 62 0.026
1000
P HML002 Hemolytic Anemia 62 0.026
1001
c NRF019 Neurofibromatosis, Type 2 62 0.026
1002
P LYM026 Lymphoblastic Leukemia 62 0.026
1003
SKN019 Skin Melanoma 62 0.026
1004
ACN011 Acne 62 0.026
1005
c LNG044 Long Qt Syndrome 1 62 0.026
1006
HSH003 Hashimoto Thyroiditis 62 0.026
1007
P ALP009 Alopecia Areata 62 0.026
1008
P PSR002 Psoriasis 61 0.026
1009
P ESP024 Esophagitis 61 0.026
1010
c SRC025 Sarcoidosis 1 61 0.026
1011
P HYP117 Hypertriglyceridemia 61 0.026
1012
P DNT015 Dent Disease 61 0.026
1013
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.026
1014
P RCK004 Rickets 61 0.026
1015
KRN002 Kearns-Sayre Syndrome 61 0.026
1016
TTN003 Tetanus 61 0.026
1017
P HYP055 Hypoplastic Left Heart Syndrome 61 0.026
1018
P SYS005 Systemic Scleroderma 61 0.026
1019
c LCL006 Localized Scleroderma 61 0.026
1020
PRD007 Periodontal Disease 60 0.026
1021
c VRL010 Viral Hepatitis 60 0.026
1022
FLL027 Fallopian Tube Carcinoma 60 0.026
1023
P PLC011 Pilocytic Astrocytoma 60 0.026
1024
CHL123 Chlamydia 60 0.026
1025
CRV038 Cervical Squamous Cell Carcinoma 60 0.026
1026
P VNT002 Ventricular Septal Defect 60 0.026
1027
P NRN021 Neuronal Ceroid Lipofuscinosis 59 0.026
1028
c MNN043 Meningioma, Familial 59 0.026
1029
KRT001 Keratoconjunctivitis Sicca 59 0.026
1030
c HPT003 Hepatitis a 59 0.026
1031
CRN036 Craniopharyngioma 59 0.026
1032
INT066 Interstitial Lung Disease 59 0.026
1033
c GCH015 Gaucher Disease, Type I 59 0.026
1034
P PRP029 Porphyria 59 0.026
1035
CMM005 Common Cold 59 0.026
1036
c EXD008 Exudative Vitreoretinopathy 1 59 0.026
1037
P CTR002 Cataract 58 0.026
1038
P BRS044 Breast Adenocarcinoma 58 0.026
1039
P MTR012 Mitral Valve Disease 58 0.026
1040
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.026
1041
c LNG047 Long Qt Syndrome 2 57 0.026
1042
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.026
1043
P LRY044 Larynx Cancer 57 0.026
1044
ALP008 Alopecia 57 0.026
1045
ORL015 Oral Squamous Cell Carcinoma 57 0.026
1046
THR024 Thrombosis 57 0.026
1047
PNC033 Pancreas Adenocarcinoma 57 0.026
1048
MSC077 Muscle Eye Brain Disease 57 0.026
1049
c ACT210 Acute Respiratory Distress Syndrome 57 0.026
1050
c SVR001 Severe Acute Respiratory Syndrome 57 0.026
1051
P HMR003 Hemorrhagic Disease 57 0.026
1052
P INT143 Interstitial Cystitis 57 0.026
1053
STR026 Star Syndrome 57 0.026
1054
PLY023 Polycystic Liver Disease 56 0.026
1055
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.026
1056
PLS011 Plasmacytoma 56 0.026
1057
P ACT074 Acute Lymphocytic Leukemia 56 0.026
1058
P SML001 Small Cell Carcinoma 56 0.026
1059
P OLG002 Oligodendroglioma 56 0.026
1060
c MYT020 Myotonic Dystrophy 2 56 0.026
1061
P GST044 Gastritis 56 0.026
1062
P SPR098 Supranuclear Palsy, Progressive 56 0.026
1063
INT079 Intrahepatic Cholangiocarcinoma 56 0.026
1064
IDP011 Idiopathic Interstitial Pneumonia 56 0.026
1065
BLD034 Bile Duct Carcinoma 56 0.026
1066
JNT002 Joint Disorders 55 0.026
1067
DBT010 Diabetic Neuropathy 55 0.026
1068
c SPN294 Spinocerebellar Ataxia 1 55 0.026
1069
P TMT001 Timothy Syndrome 55 0.026
1070
P HYP076 Hyperthyroidism 55 0.026
1071
MLN007 Male Infertility 55 0.026
1072
GLS001 Gliosarcoma 55 0.026
1073
ERY003 Erythema Multiforme 55 0.026
1074
c THR092 Thrombophilia Due to Thrombin Defect 54 0.026
1075
PLM012 Pulmonary Sarcoidosis 54 0.026
1076
CCH002 Coach Syndrome 54 0.026
1077
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 54 0.026
1078
c BCT007 Bacterial Meningitis 54 0.026
1079
c VRL007 Viral Encephalitis 54 0.026
1080
PRP083 Porphyria, Acute Intermittent 54 0.026
1081
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.026
1082
P OCL002 Oculocutaneous Albinism 54 0.026
1083
PRG097 Paragangliomas 1, with or Without Deafness 54 0.026
1084
SML033 Small Cell Cancer of the Lung, Somatic 54 0.026
1085
P THY097 Thyroid Hormone Resistance 54 0.026
1086
CRV040 Cervix Carcinoma 53 0.026
1087
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.026
1088
FRB001 Farber Lipogranulomatosis 53 0.026
1089
PRT014 Protein S Deficiency 53 0.026
1090
LYM040 Lymphoblastic Lymphoma 53 0.026
1091
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.026
1092
P EPN002 Ependymoma 53 0.026
1093
AGN012 Agnathia-Otocephaly Complex 53 0.026
1094
P LPC002 Lip Cancer 53 0.026
1095
P EXP004 Exophthalmos 53 0.026
1096
SCT005 Scott Syndrome 53 0.026
1097
P CRV031 Cervical Adenocarcinoma 53 0.026
1098
P SYP003 Syphilis 53 0.026
1099
P DBT005 Diabetes Insipidus 53 0.026
1100
THR016 Thrombophlebitis 53 0.026
1101
NRF007 Neurofibroma 53 0.026
1102
CYS010 Cystinosis 53 0.026
1103
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.026
1104
ACH005 Achalasia 52 0.026
1105
P SML016 Small Intestine Cancer 52 0.026
1106
GTR002 Goiter 52 0.026
1107
KRT006 Keratoconjunctivitis 52 0.026
1108
KRT002 Keratomalacia 52 0.026
1109
QDR001 Quadriplegia 52 0.026
1110
c HPT015 Hepatitis D 52 0.026
1111
c INF023 Inflammatory Breast Carcinoma 52 0.026
1112
GST040 Gastric Adenocarcinoma 52 0.026
1113
HMG005 Hemoglobinopathy 52 0.026
1114
c XRD019 Xeroderma Pigmentosum, Group C 52 0.026
1115
SSM001 Sesame Syndrome 52 0.026
1116
PRT011 Protein C Deficiency 52 0.026</