Search results for Risperidone

788 hits were found for Risperidone

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 74 30.533
2
PSY004 Psychotic Disorder 66 18.082
3
SCH012 Schizoaffective Disorder 49 17.027
4
P BPL003 Bipolar Disorder 56 16.041
5
c MJR022 Major Affective Disorder 8 37 15.881
6
c MJR024 Major Affective Disorder 9 40 15.881
7
SCH003 Schizophreniform Disorder 54 13.058
8
P ATS364 Autism 72 11.563
9
HYP020 Hyperprolactinemia 63 10.459
10
TRD006 Tardive Dyskinesia 53 9.122
11
P ATT013 Attention Deficit-Hyperactivity Disorder 65 9.011
12
c ATS007 Autism Spectrum Disorder 71 8.987
13
P MJR007 Major Affective Disorder 1 42 8.438
14
MNT002 Mental Depression 56 8.091
15
DSS008 Disease of Mental Health 74 7.976
16
c BPL002 Bipolar I Disorder 47 7.719
17
P PRK039 Parkinsonism 55 7.713
18
P MJR001 Major Depressive Disorder 68 7.316
19
c MJR006 Major Affective Disorder 5 32 7.251
20
c MJR003 Major Affective Disorder 6 32 7.251
21
P PRV006 Pervasive Developmental Disorder 52 7.204
22
DPR016 Depression 64 7.168
23
P DMN002 Dementia 65 7.024
24
SXL003 Sexual Disorder 49 6.771
25
MDD011 Mood Disorder 61 6.672
26
SBC016 Subacute Delirium 42 6.615
27
P DYS154 Dystonia 64 6.548
28
c MJR008 Major Affective Disorder 2 34 6.548
29
c MJR023 Major Affective Disorder 7 33 6.548
30
c MJR004 Major Affective Disorder 4 28 6.548
31
CND002 Conduct Disorder 50 6.414
32
NRL004 Neuroleptic Malignant Syndrome 52 6.397
33
P MVM001 Movement Disease 61 6.338
34
OBS002 Obsessive-Compulsive Disorder 67 6.200
35
PST028 Post-Traumatic Stress Disorder 58 6.032
36
P SBS003 Substance Abuse 54 5.948
37
P ALZ034 Alzheimer Disease 87 5.580
38
P PRS038 Personality Disorder 65 5.282
39
ANX010 Anxiety 70 5.262
40
PRN009 Paranoid Schizophrenia 49 5.239
41
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.144
42
ACT084 Acute Stress Disorder 53 5.064
43
NRT001 Neurotic Disorder 56 5.018
44
VSC002 Vascular Dementia 59 4.906
45
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 4.857
46
P TCD001 Tic Disorder 50 4.704
47
OPP004 Oppositional Defiant Disorder 48 4.636
48
GLL008 Gilles De La Tourette Syndrome 64 4.522
49
CCN001 Cocaine Dependence 47 4.396
50
P TRM003 Tremor 50 4.394
51
AMN001 Amenorrhea 53 4.202
52
GNR004 Generalized Anxiety Disorder 54 4.153
53
END040 Endogenous Depression 54 4.003
54
P PNC025 Panic Disorder 52 3.989
55
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.989
56
GLC096 Galactorrhea 40 3.983
57
HYP066 Hyperglycemia 60 3.976
58
CCN002 Cocaine Abuse 49 3.958
59
ADL002 Adult Syndrome 69 3.905
60
48X005 48,xyyy 39 3.854
61
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.817
62
P KHL003 Kohlschutter-Tonz Syndrome 57 3.813
63
P HNT016 Huntington Disease 73 3.810
64
c TYP009 Type 2 Diabetes Mellitus 91 3.695
65
BRD004 Borderline Personality Disorder 53 3.613
66
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 3.596
67
DLS001 Delusional Disorder 44 3.487
68
SCH011 Schizotypal Personality Disorder 36 3.443
69
PRP007 Priapism 46 3.408
70
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 3.352
71
CHR073 Choreatic Disease 53 3.352
72
AVD001 Avoidant Personality Disorder 49 3.350
73
CHL079 Children's Interstitial Lung Disease 25 3.331
74
AND005 Androgen Insensitivity Syndrome, Mild 21 3.276
75
EPT021 Epithelial Recurrent Erosion Dystrophy 45 3.241
76
P TRN020 Turner Syndrome 67 3.145
77
P ALC033 Alcohol Use Disorder 67 3.096
78
DWN001 Down Syndrome 70 3.015
79
NTR005 Nutritional Deficiency Disease 60 3.002
80
P ANR048 Aniridia 1 66 2.995
81
ANR007 Anorexia Nervosa 59 2.993
82
INF021 Infant Gynecomastia 30 2.975
83
GYN001 Gynecomastia 48 2.975
85
ALC007 Alcohol Dependence 65 2.941
86
AGN016 Aging 53 2.899
87
IMP005 Impotence 52 2.876
88
P SLP005 Sleep Disorder 61 2.868
89
CNS004 Constipation 56 2.830
90
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.819
91
P ASP001 Asperger Syndrome 48 2.773
92
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 2.771
93
GRN017 Granulocytopenia 42 2.698
94
P DBT009 Diabetes Mellitus 67 2.691
95
LPD008 Lipid Metabolism Disorder 61 2.581
96
RHB024 Rhabdomyosarcoma 2 65 2.531
97
CNN001 Cannabis Dependence 37 2.443
98
c CHR056 Chronic Tic Disorder 36 2.416
99
DBT084 Diabetes Mellitus, Ketosis-Prone 59 2.374
100
LNG015 Lingual-Facial-Buccal Dyskinesia 47 2.362
101
OPT003 Opiate Dependence 49 2.349
102
P NTR004 Neutropenia 62 2.327
103
P SZR006 Seizure Disorder 69 2.325
104
c ERL020 Early-Onset Schizophrenia 43 2.320
105
MLN003 Melancholia 41 2.314
106
STT041 Stuttering 52 2.289
107
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 2.244
108
ANT039 Antisynthetase Syndrome 55 2.244
109
P PRK057 Parkinson Disease, Late-Onset 79 2.210
110
SRT004 Serotonin Syndrome 54 2.176
111
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 2.160
112
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 2.160
113
PRT058 Pure Autonomic Failure 58 2.153
114
TRM010 Traumatic Brain Injury 50 2.142
115
AMP007 Amphetamine Abuse 36 2.134
116
LRN003 Learning Disability 49 2.134
117
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.118
118
ADJ001 Adjustment Disorder 46 2.075
119
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 2.075
120
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.075
121
IMP006 Impulse Control Disorder 44 2.049
122
HYP005 Hypokalemia 55 2.023
123
P RHN004 Rhinitis 56 1.997
124
OCL069 Ocular Motor Apraxia 57 1.990
125
ETN001 Eating Disorder 59 1.986
126
CYT002 Cytokine Deficiency 43 1.961
127
P URN019 Urinary Tract Infection 48 1.953
128
P HYP750 Hypertriglyceridemia, Familial 61 1.900
129
P PNC044 Pancreatitis 61 1.889
130
ATX019 Ataxia with Vitamin E Deficiency 44 1.837
131
ATR057 Atrioventricular Block 54 1.824
132
CNN002 Cannabis Abuse 44 1.822
133
47X002 47,xyy 47 1.812
134
BRN071 Brain Injury 50 1.812
135
GLC003 Glucose Intolerance 53 1.798
136
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.775
137
DYS073 Dysphagia 53 1.772
138
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.716
139
c BLD140 Blood Group, I System 47 1.716
140
P EPL164 Epilepsy 70 1.688
141
HYP080 Hypogonadism 49 1.686
142
P FRG001 Fragile X Syndrome 70 1.665
143
P ENC018 Encephalopathy 62 1.649
144
P NRB001 Neuroblastoma 66 1.628
145
P RTT002 Rett Syndrome 79 1.622
146
CRD132 Cardiac Conduction Defect 59 1.619
147
ACQ007 Acquired Immunodeficiency Syndrome 58 1.604
148
P CRD119 Cardiac Arrest 68 1.598
149
CHR682 Chronic Bilirubin Encephalopathy 37 1.571
150
CYT018 Cytochrome P450 2d6 Variant 26 1.568
151
DGR001 Digeorge Syndrome 62 1.534
152
P LNG028 Long Qt Syndrome 63 1.512
153
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.490
154
WLL001 Williams-Beuren Syndrome 60 1.489
155
P PNM007 Pneumonia 64 1.479
156
IRN002 Iron Metabolism Disease 56 1.468
157
PTT037 Pituitary Tumors 44 1.460
158
CRB039 Cerebrovascular Disease 65 1.452
159
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.448
160
TRC010 Trichotillomania 51 1.432
161
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.431
162
DYS009 Dysthymic Disorder 51 1.431
163
HYP264 Hypertonia 35 1.422
164
DMN031 Dementia, Lewy Body 65 1.419
165
P EXN002 Exanthem 58 1.392
166
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.392
167
SYN036 Syncope 44 1.392
168
VLC001 Velocardiofacial Syndrome 57 1.384
169
MRD002 Marden-Walker Syndrome 56 1.384
170
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 1.384
171
CGN007 Cognitive Function 1, Social 27 1.384
172
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 1.384
173
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.384
174
MRF001 Marfan Syndrome 76 1.384
175
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 1.384
176
P CRN037 Craniosynostosis 67 1.384
177
TRN015 Transient Cerebral Ischemia 62 1.363
178
P PRD006 Prader-Willi Syndrome 60 1.348
179
P ANG015 Angioedema 56 1.333
180
INT075 Intracranial Hypertension 52 1.333
181
PHY002 Physical Disorder 40 1.313
182
c ACT027 Acute Pancreatitis 60 1.313
183
c SCH082 Schizophrenia 5 23 1.232
184
P MYC033 Myoclonus 46 1.232
185
STR067 Stroke, Ischemic 79 1.231
186
SCH036 Scheie Syndrome 73 1.225
187
HYP014 Hyperuricemia 51 1.215
188
P PTS002 Ptosis 52 1.201
189
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 1.201
190
P LVR013 Liver Disease 68 1.201
191
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.169
192
P PTT006 Pituitary Adenoma 55 1.169
193
ATM095 Autoimmune Disease 61 1.168
194
P BLP003 Blepharospasm 45 1.149
195
DPS001 Dipsogenic Diabetes Insipidus 21 1.149
196
c SCH079 Schizophrenia 1 44 1.145
197
SCL003 Social Phobia 48 1.145
198
SBS004 Substance Dependence 46 1.145
199
RCK004 Rickets 64 1.143
200
SVR004 Severe Combined Immunodeficiency 70 1.132
201
ACT088 Acute Insulin Response 39 1.130
202
P THR014 Thrombocytopenia 66 1.130
203
CRB037 Cerebral Palsy 66 1.105
204
P HYP086 Hypothyroidism 68 1.091
205
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 1.081
206
SMT001 Somatization Disorder 49 1.078
207
TBC004 Tobacco Addiction 63 1.077
208
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.077
209
P RSP003 Respiratory Failure 73 1.077
210
MTS001 Mutism 44 1.077
211
PLM033 Pulmonary Embolism 58 1.077
212
P HDC001 Headache 56 1.077
213
PRS063 Paresthesia 39 1.077
214
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.073
215
BNR002 Bone Resorption Disease 47 1.062
216
ATN005 Autonomic Dysfunction 45 1.062
217
P HYP263 Hypersomnia 40 1.062
218
SGM008 Segmental Dystonia 28 1.061
219
LSC001 Lesch-Nyhan Syndrome 62 1.061
220
MST005 Mastitis 52 1.061
221
GRN033 Granulomatous Mastitis 31 1.061
222
P CHR345 Chronic Pain 50 1.046
223
MTB004 Metabolic Acidosis 48 1.012
224
HYP060 Hyperinsulinism 53 1.012
225
ALL029 Allergic Disease 61 1.012
226
SPS016 Spasmodic Dysphonia 32 1.012
227
P HYP265 Hypotonia 42 1.012
228
GLL048 Glial Tumor 51 1.012
229
ERY003 Erythema Multiforme 56 0.999
230
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.994
231
c SCH061 Schizophrenia 16 24 0.994
232
CHL068 Cholestasis 61 0.994
233
c TYP008 Type 1 Diabetes Mellitus 77 0.974
234
ANT011 Antisocial Personality Disorder 47 0.974
235
FTT001 Fatty Liver Disease 61 0.974
236
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.954
237
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.954
238
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.954
239
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.954
240
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.954
241
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.954
242
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.954
243
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.954
244
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.954
245
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.954
246
STT001 Status Epilepticus 58 0.953
247
P ESN008 Eosinophilic Pneumonia 50 0.953
248
CHR158 Charles Bonnet Syndrome 23 0.953
249
OCL066 Oculogyric Crisis 35 0.931
250
P MYS003 Myasthenia Gravis 67 0.931
251
PPL049 Papillon-Lefevre Syndrome 65 0.930
252
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.930
253
HMN044 Human Immunodeficiency Virus Type 1 76 0.930
254
KRT002 Keratomalacia 54 0.930
255
c THR092 Thrombophilia Due to Thrombin Defect 74 0.929
256
MCL057 Macular Dystrophy with Central Cone Involvement 28 0.929
257
CNV002 Conversion Disorder 47 0.929
258
P CTR002 Cataract 59 0.906
259
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.902
260
P SLP006 Sleep Apnea 69 0.902
261
P MLT020 Multiple Sclerosis 79 0.902
262
CHL078 Childhood-Onset Schizophrenia 29 0.902
263
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.893
264
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.893
265
P KBK002 Kabuki Syndrome 1 66 0.893
266
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 43 0.893
267
OPD001 Opioid Abuse 44 0.893
268
SMT006 Somatoform Disorder 50 0.893
269
GST020 Gastric Antral Vascular Ectasia 40 0.893
270
VSL002 Visual Epilepsy 39 0.893
271
OBS003 Obsessive-Compulsive Personality Disorder 43 0.893
272
NRN002 Neuronitis 31 0.893
273
DRG016 Drug Induced Dyskinesia 23 0.893
274
c SCH085 Schizophrenia 2 27 0.888
275
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.877
276
LYM027 Lymphopenia 56 0.877
277
PRT037 Pertussis 49 0.877
278
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.874
279
P OST002 Osteoporosis 76 0.874
280
c SCH084 Schizophrenia 8 27 0.874
281
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.874
282
HMR023 Hemorrhagic Cystitis 43 0.848
283
P CYS018 Cystitis 58 0.848
284
P CRN300 Coronary Heart Disease 1 73 0.843
285
c SCH051 Schizophrenia 4 35 0.843
286
ADN018 Adenoma 58 0.843
287
P HYD006 Hydrocephalus 62 0.843
288
CRB004 Cerebral Artery Occlusion 45 0.843
289
P HYP098 Hypereosinophilic Syndrome 66 0.843
290
IMM167 Immune Deficiency Disease 76 0.843
291
ISC004 Ischemia 61 0.843
292
P URT039 Urticaria 57 0.843
293
MLD018 Mild Cognitive Impairment 48 0.827
294
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.809
295
P RST001 Restless Legs Syndrome 52 0.809
296
SPS134 Spasmodic Dystonia 28 0.809
297
ALL014 Allergic Encephalomyelitis 34 0.809
298
ADG002 Audiogenic Seizures 25 0.809
299
c SYS001 Systemic Lupus Erythematosus 85 0.799
300
P CMP008 Compartment Syndrome 49 0.799
301
P LPS004 Lupus Erythematosus 61 0.799
302
CHR281 Chronic Hiccups 29 0.799
303
WTH001 Withdrawal Disorder 47 0.791
304
PHN003 Phenylketonuria 76 0.791
305
BNB002 Bainbridge-Ropers Syndrome 45 0.791
306
GST023 Gastric Ulcer 52 0.791
307
GLM045 Glioma 62 0.791
308
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.791
309
ACT181 Acute Motor Axonal Neuropathy 25 0.791
310
HND015 Hand Skill, Relative 29 0.772
311
c SCH045 Schizophrenia 12 23 0.772
312
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.772
313
MCS002 Mucositis 55 0.772
314
THR024 Thrombosis 56 0.772
315
MCL006 Macular Retinal Edema 56 0.772
316
P HRT032 Heart Disease 84 0.772
317
c HPT003 Hepatitis a 63 0.772
318
BRN024 Bronchitis 67 0.772
319
STM007 Stomatitis 52 0.772
320
SBS005 Substance-Induced Psychosis 31 0.772
321
CLT003 Colitis 63 0.751
322
BSL009 Basal Ganglia Calcification 45 0.751
323
CFF002 Coffin-Lowry Syndrome 59 0.751
324
DSS032 Disease by Infectious Agent 55 0.751
325
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.751
326
MGC001 Megacolon 48 0.751
327
P ACN011 Acne 55 0.751
328
CHL012 Childhood Disintegrative Disease 44 0.751
329
c MCP001 Mucopolysaccharidosis Iii 69 0.751
330
NSP002 Nasopharyngitis 45 0.751
331
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.728
332
c LYM145 Lymphatic Malformation 5 48 0.728
333
VTM002 Vitamin B12 Deficiency 48 0.728
334
c ATS371 Autism 6 21 0.728
335
DYS192 Dystonia, Dopa-Responsive 56 0.728
336
PHL006 Phelan-Mcdermid Syndrome 61 0.728
337
SCH004 Schizoid Personality Disorder 27 0.728
338
P KDN018 Kidney Disease 71 0.728
339
P MTC069 Mitochondrial Disorders 57 0.728
340
RYN005 Raynaud Phenomenon 45 0.728
341
PHN011 Phenytoin Toxicity 32 0.703
342
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.703
343
P CLR023 Colorectal Cancer 100 0.703
344
P TRT019 Torticollis 47 0.703
345
GLB001 Gilbert Syndrome 53 0.703
346
P PHC003 Pheochromocytoma 70 0.703
347
c RTN042 Retinitis Pigmentosa 12 42 0.703
348
ADR040 Adrenal Gland Pheochromocytoma 45 0.703
349
PHR003 Pharyngitis 57 0.703
350
P LPS002 Liposarcoma 64 0.703
351
P HPT021 Hepatitis 68 0.703
352
SPR012 Separation Anxiety Disorder 41 0.703
353
P SCK005 Sickle Cell Disease 56 0.703
354
HYP056 Hypoglycemia 65 0.703
356
RRM016 Rare Movement Disorder 15 0.703
357
MYT011 Myotonia 37 0.703
358
CVD001 Covid-19 59 0.701
359
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.674
360
MYX004 Myxedema 43 0.674
361
c RTN047 Retinitis Pigmentosa 18 45 0.674
362
NRD029 Neurodevelopmental Disorder with Involuntary Movements 25 0.674
363
c SCH053 Schizophrenia 13 27 0.674
364
c GLL024 Gallbladder Disease 1 53 0.674
365
ACN002 Acanthosis Nigricans 56 0.674
366
P RTN022 Retinal Vein Occlusion 54 0.674
367
BRN009 Burning Mouth Syndrome 51 0.674
368
c VRL010 Viral Hepatitis 52 0.674
369
HRT012 Heart Valve Disease 53 0.674
370
CNT016 Central Retinal Vein Occlusion 53 0.674
371
ALC013 Alcohol-Induced Mental Disorder 19 0.674
372
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.674
373
P INT070 Intestinal Obstruction 57 0.674
374
ILS001 Ileus 49 0.674
375
PRL008 Paralytic Ileus 44 0.674
376
P ENC004 Encephalitis 61 0.674
377
END086 End Stage Renal Disease 54 0.674
378
MLT131 Multifocal Atrial Tachycardia 18 0.674
379
BDY001 Body Dysmorphic Disorder 40 0.640
380
BLM002 Bulimia Nervosa 56 0.640
381
PNG002 Pain Agnosia 51 0.640
382
ATS010 Autosomal Recessive Disease 42 0.640
383
P LKM062 Leukemia, Acute Lymphoblastic 69 0.640
384
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.640
385
P BND020 Bone Disease 60 0.640
386
P NPH012 Nephrotic Syndrome 61 0.640
387
ASY002 Asymptomatic Neurosyphilis 41 0.640
388
P LTR001 Lateral Sclerosis 57 0.640
389
LYM017 Lyme Disease 63 0.640
390
P EHL001 Ehlers-Danlos Syndrome 57 0.640
391
HSH004 Hashimoto Encephalopathy 29 0.640
392
HYP144 Hyperacusis 23 0.640
393
NRS003 Neurosyphilis 45 0.640
394
LWF001 Low-Flow Priapism 16 0.640
395
SVR001 Severe Acute Respiratory Syndrome 68 0.624
397
P JBR020 Joubert Syndrome 1 74 0.596
398
c ATR087 Atrial Standstill 1 74 0.596
399
MLT010 Multiple Personality Disorder 29 0.596
400
c ATM011 Autoimmune Hepatitis 62 0.596
401
ACR007 Acromegaly 70 0.596
402
P TBR001 Tuberous Sclerosis 69 0.596
403
CYS005 Cysticercosis 60 0.596
404
BRS051 Breast Disease 58 0.596
405
CRT015 Carotid Artery Occlusion 45 0.596
406
NRM001 Neuromyelitis Optica 60 0.596
407
P PLY017 Polyarteritis Nodosa 59 0.596
408
DRG003 Drug Dependence 46 0.596
409
GST092 Gastroesophageal Reflux 59 0.590
410
c HYP595 Hypertension, Essential 84 0.546
411
DFC004 Deficiency Anemia 74 0.490
412
TRT017 Teratoma, Ovarian 28 0.490
413
P EPS030 Episodic Kinesigenic Dyskinesia 1 55 0.490
414
SMT008 Smith-Magenis Syndrome 53 0.490
415
P PLM037 Pulmonary Hypertension 69 0.490
416
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.490
417
WLF001 Wolff-Parkinson-White Syndrome 63 0.490
418
INT303 Intracranial Hypertension, Idiopathic 56 0.490
419
P PTT014 Pitt-Hopkins Syndrome 63 0.490
420
P LKM002 Leukemia 65 0.490
421
DRG002 Drug-Induced Hepatitis 42 0.490
422
NRS005 Neurosarcoidosis 32 0.490
423
OVR109 Ovarian Germ Cell Teratoma 32 0.490
424
MGL001 Megaloblastic Anemia 59 0.490
425
PDP001 Pedophilia 28 0.490
426
P TRT010 Teratoma 50 0.490
427
P HYP061 Hypertrophic Cardiomyopathy 68 0.490
428
PMP014 Pemphigoid 48 0.490
429
ANH002 Anhidrosis 45 0.490
430
BRN026 Branch Retinal Artery Occlusion 41 0.490
431
BLL006 Bullous Pemphigoid 61 0.490
432
P NRF002 Neurofibromatosis 60 0.490
433
P RTN014 Retinal Artery Occlusion 46 0.490
434
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.490
435
PST086 Posterior Cortical Atrophy 36 0.490
436
GBM001 Gaba Aminotransferase Deficiency 31 0.440
437
P FNG006 Feingold Syndrome 1 61 0.440
438
c SML038 Small Cell Cancer of the Lung 68 0.440
439
P NJM001 Nijmegen Breakage Syndrome 75 0.440
440
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.440
441
c PNS012 Paine Syndrome 60 0.440
442
P CRB154 Cerebrocostomandibular Syndrome 55 0.440
443
DNT045 Dental Anomalies and Short Stature 50 0.440
444
HYP025 Hyperphosphatemia 47 0.440
445
ANG049 Angioedema Induced by Ace Inhibitors 38 0.440
446
P LNG032 Lung Cancer 98 0.440
447
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.440
448
IMM240 Immunodeficiency 14a, Autosomal Dominant 52 0.440
449
KWS002 Kawasaki Disease 65 0.440
450
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.440
451
IMM102 Immunodeficiency 14 51 0.440
452
DSS010 Dissociative Disorder 39 0.440
453
BLD051 Blood Coagulation Disease 52 0.440
454
c CNT035 Central Nervous System Disease 53 0.440
455
CNN003 Conn's Syndrome 77 0.440
456
c ACT068 Acute Cystitis 60 0.440
457
TXC002 Toxic Encephalopathy 51 0.440
458
BSL008 Basal Ganglia Disease 41 0.440
459
BRN056 Bronchopulmonary Dysplasia 57 0.440
460
P NRV007 Nervous System Disease 65 0.440
461
c HYP836 Hypercholesterolemia, Familial, 1 73 0.426
462
GST033 Gestational Diabetes 60 0.354
463
SPC030 Specific Language Disorder 25 0.337
464
ATH004 Athetosis 25 0.320
465
P MYC008 Myocarditis 59 0.320
466
c MGR028 Migraine with or Without Aura 1 63 0.302
467
CRD223 Cardiac Arrhythmia 63 0.302
468
P MYP004 Myopathy 67 0.302
469
ASP007 Aspiration Pneumonia 49 0.282
470
P TMP001 Temporal Lobe Epilepsy 49 0.282
471
OLG001 Oligospermia 45 0.282
472
KLN009 Kleine-Levin Hibernation Syndrome 37 0.261
473
c SCH080 Schizophrenia 3 27 0.261
474
P ART021 Arteriosclerosis 53 0.261
475
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.261
476
XRP001 Xerophthalmia 42 0.261
477
KRT001 Keratoconjunctivitis Sicca 49 0.261
478
P NRC002 Narcolepsy 55 0.261
479
P HYP076 Hyperthyroidism 53 0.261
480
P HRP006 Herpes Simplex 65 0.261
481
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.238
482
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.238
483
FRN006 Frontotemporal Dementia 68 0.238
484
MTN003 Motion Sickness 50 0.238
485
c ACT071 Acute Kidney Failure 60 0.238
486
CNG034 Congestive Heart Failure 69 0.238
487
P AGN002 Agnosia 53 0.238
488
HYP016 Hypochondriasis 47 0.238
489
P MLG056 Malignant Hyperthermia 65 0.238
490
DBT010 Diabetic Neuropathy 54 0.238
491
HRN003 Heroin Dependence 44 0.238
492
c FML191 Familial Long Qt Syndrome 54 0.238
493
PSD088 Pseudobulbar Affect 33 0.238
494
HDN002 Head Injury 44 0.238
495
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 0.213
496
c SCH083 Schizophrenia 7 29 0.213
497
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.213
498
DNT012 Dental Caries 53 0.213
499
GLB002 Glioblastoma 67 0.213
500
DFF002 Diffuse Pulmonary Fibrosis 27 0.213
501
P PLM036 Pulmonary Fibrosis 65 0.213
502
P ADL010 Adult Respiratory Distress Syndrome 70 0.213
503
P VSC011 Vasculitis 61 0.213
504
SPC005 Speech Disorder 46 0.213
505
TXC010 Toxic Myocarditis 23 0.213
506
LNG099 Lung Disease 62 0.213
507
c SCH073 Schizophrenia 9 25 0.185
508
APH002 Aphasia 55 0.185
509
P PRS040 Prostate Cancer 95 0.185
510
c SCH081 Schizophrenia 6 27 0.185
511
CYN002 Cyanosis, Transient Neonatal 43 0.185
512
c THY107 Thymoma, Familial 42 0.185
513
CYC008 Cyclic Vomiting Syndrome 46 0.185
514
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.185
515
PTH002 Pathological Gambling 48 0.185
516
P THY023 Thymoma 64 0.185
517
PNM008 Pneumothorax 54 0.185
518
FBR047 Fibromyalgia 57 0.185
519
P PLY011 Polycystic Ovary Syndrome 57 0.185
520
P GST044 Gastritis 55 0.185
521
KLV001 Kluver-Bucy Syndrome 34 0.185
522
PLM010 Pulmonary Edema 54 0.185
523
AMN003 Amnestic Disorder 53 0.185
524
PRS045 Prostatic Hypertrophy 53 0.185
525
P MCR010 Microcephaly 59 0.185
526
TXC005 Toxic Shock Syndrome 61 0.185
527
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.185
528
CYC005 Cyclothymic Disorder 40 0.185
529
P RTN016 Retinal Degeneration 52 0.185
530
BCK006 Back Pain 43 0.185
531
IRR002 Irritable Bowel Syndrome 64 0.185
532
MTR086 Motor Stereotypies 14 0.185
533
PST103 Postpartum Psychosis 31 0.185
534
SPS057 Spasticity 43 0.185
535
VSL003 Visual Agnosia 33 0.151
536
P SCL018 Scoliosis 57 0.151
537
CRH005 Crohn's Colitis 53 0.151
538
CRV043 Cervical Dystonia 46 0.151
539
ART002 Arts Syndrome 66 0.151
540
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.151
542
P TYS001 Tay-Sachs Disease 69 0.151
543
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.151
544
P MYM013 Moyamoya Disease 1 59 0.151
545
c SCH056 Schizophrenia 15 38 0.151
546
MNN043 Meningioma, Familial 79 0.151
547
P GLM040 Glioma Susceptibility 1 70 0.151
548
P HPT023 Hepatocellular Carcinoma 95 0.151
549
CHD004 Chudley-Mccullough Syndrome 47 0.151
550
P CRB045 Cerebellar Hypoplasia 40 0.151
551
DSS009 Disseminated Intravascular Coagulation 56 0.151
552
NNL006 Non-Alcoholic Steatohepatitis 54 0.151
553
FCL014 Focal Epilepsy 53 0.151
554
MLG169 Malignant Astrocytoma 57 0.151
555
BLR008 Bilirubin Metabolic Disorder 57 0.151
556
c TRN005 Transient Tic Disorder 17 0.151
557
INT025 Intermittent Explosive Disorder 39 0.151
558
P BNC003 Bone Cancer 58 0.151
559
BCT022 Bacterial Infectious Disease 55 0.151
560
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.151
561
ANT019 Anterograde Amnesia 38 0.151
562
ASP008 Aspiration Pneumonitis 43 0.151
563
GLS007 Glossitis 46 0.151
564
c HPT001 Hepatitis C 61 0.151
565
SCR001 Secretory Meningioma 40 0.151
566
PYD002 Pyoderma 49 0.151
567
P SYP003 Syphilis 59 0.151
568
BRX001 Bruxism 50 0.151
569
ANV001 Anovulation 46 0.151
570
LYS002 Lysosomal Storage Disease 51 0.151
571
P BRS044 Breast Adenocarcinoma 58 0.151
572
TST014 Testicular Cancer 51 0.151
573
GLC008 Glucose Metabolism Disease 40 0.151
574
INT395 Intracranial Meningioma 47 0.151
575
c CHR054 Chronic Closed-Angle Glaucoma 33 0.151
576
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.151
577
PYD001 Pyoderma Gangrenosum 53 0.151
578
PRT036 Peritonitis 65 0.151
579
INT007 Intermediate Coronary Syndrome 53 0.151
580
GNT003 Genital Herpes 54 0.151
581
CRH001 Crohn's Disease 80 0.151
582
HRP009 Herpes Simplex Encephalitis 58 0.151
583
P THL005 Thalassemia 56 0.151
584
P MSC005 Muscular Dystrophy 66 0.151
585
P ALP008 Alopecia 53 0.151
586
ANX004 Anoxia 40 0.151
587
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.151
588
SYS071 Systemic Autoimmune Disease 35 0.151
589
PSD079 Pseudoangiomatous Stromal Hyperplasia 19 0.151
590
P FBR031 Febrile Seizures 52 0.151
591
THY029 Thyroid Carcinoma 55 0.151
592
APR001 Apraxia 51 0.107
594
c LPR022 Leprosy 2 35 0.107
595
P ATR011 Atrial Fibrillation 66 0.107
596
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.107
597
c SCH064 Schizophrenia 10 27 0.107
598
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 55 0.107
599
EMN001 Emanuel Syndrome 33 0.107
600
PLY028 Polycystic Bone Disease 17 0.107
601
FRS012 First-Degree Atrioventricular Block 39 0.107
602
SCN049 Second-Degree Atrioventricular Block 34 0.107
603
HMD003 Hemidystonia 28 0.107
604
BLR027 Blue Rubber Bleb Nevus 39 0.107
605
DYG001 Dyggve-Melchior-Clausen Disease 47 0.107
606
P OVR042 Ovarian Cancer 88 0.107
607
LYM133 Lymphoma, Hodgkin, Classic 69 0.107
608
c HYD064 Hydrocephalus, Congenital, 1 51 0.107
609
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.107
610
INT372 Intellectual Developmental Disorder, X-Linked, Syndromic, Lujan-Fryns Type 32 0.107
611
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.107
612
AND002 Androgen Insensitivity Syndrome 63 0.107
613
HMC014 Homocysteinemia 52 0.107
614
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.107
615
WLS001 Wilson Disease 70 0.107
616
SPC010 Speech and Communication Disorders 47 0.107
617
P FML011 Familial Adenomatous Polyposis 70 0.107
618
P USH001 Usher Syndrome 63 0.107
619
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.107
620
P GST053 Gastric Cancer 82 0.107
621
HLX001 Helix Syndrome 47 0.107
622
P OCL002 Oculocutaneous Albinism 59 0.107
624
c ALB021 Albinism, Oculocutaneous, Type Ii 58 0.107
625
CRN264 Craniosynostosis with Fibular Aplasia 29 0.107
626
c TBR025 Tuberous Sclerosis 1 84 0.107
627
P STS008 Sotos Syndrome 1 62 0.107
628
PRP083 Porphyria, Acute Intermittent 64 0.107
629
P LPR021 Leprosy 3 71 0.107
630
P RTN008 Retinitis Pigmentosa 79 0.107
631
SMT004 Smith-Lemli-Opitz Syndrome 69 0.107
632
SDD001 Sudden Infant Death Syndrome 60 0.107
633
c GRV008 Graves Disease 1 54 0.107
634
P MNT135 Mental Retardation, X-Linked, Syndromic 13 49 0.107
635
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.107
636
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.107
637
PHB003 Phobia, Specific 44 0.107
638
P MYC007 Myocardial Infarction 69 0.107
639
P GRF003 Graft-Versus-Host Disease 71 0.107
640
c SCH087 Schizophrenia 18 28 0.107
641
LPT014 Leptin Deficiency or Dysfunction 77 0.107
642
c SCH052 Schizophrenia 14 19 0.107
643
P ANG001 Angelman Syndrome 64 0.107
644
CLF027 Cleft Palate, Isolated 64 0.107
645
ESP021 Esophageal Cancer 84 0.107
646
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 55 0.107
647
PMP006 Pemphigus Vulgaris, Familial 57 0.107
648
FRY002 Fryns Syndrome 39 0.107
649
PLY068 Polysubstance Abuse 41 0.107
650
END057 Endometrial Cancer 76 0.107
651
PRS129 Prostatic Hyperplasia, Benign 48 0.107
652
c SCH086 Schizophrenia 11 21 0.107
653
P KLZ004 Kala-Azar 1 41 0.107
654
TTH002 Tooth Agenesis 61 0.107
655
P MTP001 Metaphyseal Dysplasia 38 0.107
656
P MYG005 Myoglobinuria 40 0.107
657
CHR704 Chromosome 16p11.2 Deletion Syndrome 35 0.107
658
c SYN082 Syndromic X-Linked Intellectual Disability 14 22 0.107
659
EXH001 Exhibitionism 25 0.107
660
P MMP001 Mumps 56 0.107
661
PRS119 Persistent Genital Arousal Disorder 18 0.107
662
CRD001 Cardiac Tamponade 44 0.107
663
LTN029 Latent Autoimmune Diabetes in Adults 38 0.107
664
P ALP004 Alport Syndrome 69 0.107
665
MNN032 Meningococcal Meningitis 52 0.107
666
P PRT026 Parotitis 42 0.107
667
SLD003 Sialadenitis 47 0.107
668
PRN010 Paranoid Personality Disorder 26 0.107
669
P HYP069 Hyperparathyroidism 62 0.107
670
PRM003 Premature Ejaculation 44 0.107
671
PNC001 Pancytopenia 52 0.107
672
THR004 Thrombocytosis 52 0.107
673
P OLG002 Oligodendroglioma 66 0.107
674
P THR015 Thrombophilia 51 0.107
675
P HMN010 Hemangioma 61 0.107
676
NRT004 Neuritis 53 0.107
677
URT037 Urethral Stricture 42 0.107
678
P DSR090 Disorder of Sexual Development 45 0.107
679
P HYP730 Hypogonadotropic Hypogonadism 57 0.107
680
XLN231 X-Linked Alport Syndrome 41 0.107
681
HMP001 Hemopericardium 47 0.107
682
P END047 Endophthalmitis 53 0.107
683
GRS001 Gerstmann Syndrome 41 0.107
684
PHN001 Phencyclidine Abuse 23 0.107
685
P EYD002 Eye Disease 57 0.107
686
NPH009 Nephrolithiasis 54 0.107
687
ESP023 Esophageal Disease 52 0.107
688
PRP016 Paraplegia 52 0.107
689
HMP005 Hemiplegia 53 0.107
690
ASP004 Asphyxia Neonatorum 50 0.107
691
NRR001 Neuroretinitis 42 0.107
692
P OVR049 Ovarian Disease 50 0.107
693
KLB003 Klebsiella Pneumonia 49 0.107
694
P PRP029 Porphyria 60 0.107
695
PLM001 Pulmonary Tuberculosis 69 0.107
696
RTR001 Retrograde Amnesia 41 0.107
697
TCK004 Tick Infestation 29 0.107
698
NRM005 Neuromuscular Disease 62 0.107
699
SPN035 Spindle Cell Sarcoma 51 0.107
700
PRS021 Prostatic Adenoma 43 0.107
701
THR016 Thrombophlebitis 50 0.107
702
PLR007 Pleural Empyema 50 0.107
703
HGH043 High Grade Glioma 46 0.107
704
P GRV001 Graves' Disease 54 0.107
705
P PRC012 Pericardial Effusion 50 0.107
706
P LKD001 Leukodystrophy 58 0.107
707
PRT013 Portal Hypertension 59 0.107
708
P MTH007 Methemoglobinemia 46 0.107
709
ANG005 Anogenital Venereal Wart 55 0.107
710
c PRM005 Primary Hyperparathyroidism 59 0.107
711
MGS001 Megaesophagus 44 0.107
712
END062 Endometrial Hyperplasia 47 0.107
713
URL001 Urolithiasis 45 0.107
714
PCD001 Pica Disease 38 0.107
715
RHM001 Rheumatic Fever 59 0.107
716
IRT001 Iritis 45 0.107
717
PLS007 Plasmodium Falciparum Malaria 52 0.107
718
ACT003 Acute Kidney Tubular Necrosis 46 0.107
719
SRC014 Sarcoma 64 0.107
720
P FML340 Familial Episodic Pain Syndrome 50 0.107
721
P OPT009 Optic Neuritis 57 0.107
722
DTR001 Detrusor Sphincter Dyssynergia 37 0.107
723
GT001 Gout 63 0.107
724
SCB001 Scabies 49 0.107
725
ACT049 Acute Disseminated Encephalomyelitis 53 0.107
726
P CWD010 Cowden Syndrome 70 0.107
727
c VRL007 Viral Encephalitis 50 0.107
728
RTN023 Retinitis 45 0.107
729
SKN016 Skin Disease 63 0.107
730
CPG001 Capgras Syndrome 26 0.107
731
CMB002 Combat Disorder 33 0.107
732
ACH005 Achalasia 54 0.107
733
P PMP001 Pemphigus 54 0.107
734
P MYT002 Myotonic Dystrophy 51 0.107
736
P HMC002 Homocystinuria 52 0.107
737
LYM014 Lymphangitis 38 0.107
738
LSH001 Leishmaniasis 63 0.107
739
LTN001 Latent Syphilis 34 0.107
740
VSC003 Visceral Leishmaniasis 54 0.107
741
c ACT075 Acute Myocardial Infarction 55 0.107
742
PPT005 Peptic Ulcer Disease 58 0.107
743
TRT003 Tertiary Syphilis 36 0.107
744
HRP004 Herpes Zoster 60 0.107
745
CHR066 Chronic Fatigue Syndrome 59 0.107
746
HNS001 Hansen's Disease 32 0.107
747
P HYP120 Hypoaldosteronism 33 0.107
748
RCR002 Recurrent Hypersomnia 28 0.107
749
P TXP001 Toxoplasmosis 59 0.107
750
ALB002 Albinism 46 0.107
751
GRN059 Grn Frontotemporal Dementia 16 0.107
752
BNS003 Binswanger's Disease 41 0.107
753
CND006 Candida Glabrata 29 0.107
754
BRT037 Brittle Diabetes 24 0.107
755
BRK012 Broken Heart Syndrome 42 0.107
756
P THY032 Thyroiditis 56 0.107
757
GST050 Gastrointestinal System Disease 55 0.107
758
MRG007 Morgellons 15 0.107
759
OPD006 Opioid Addiction 48 0.107
760
P DBT005 Diabetes Insipidus 54 0.107
761
STN013 Stenotrophomonas Maltophilia Infection 26 0.107
762
UTR043 Uterine Sarcoma 40 0.107
763
DRG017 Drug-Induced Vasculitis 16 0.107
764
c BCT013 Bacterial Pneumonia 47 0.107
765
P SBR004 Seborrheic Dermatitis 44 0.107
766
PYM001 Pyomyositis 42 0.107
767
NNT008 Neonatal Abstinence Syndrome 41 0.107
768
HVY002 Heavy Metal Poisoning 22 0.107
769
INT104 Intravascular Papillary Endothelial Hyperplasia 30 0.107
770
MGR035 Migraine with Brainstem Aura 22 0.107
772
MCP054 Mecp2 Disorders 16 0.107
773
ADS004 Aids Dementia Complex 39 0.107
774
FCL090 Facial Cleft 32 0.107
775
PRG033 Progressive Non-Fluent Aphasia 52 0.107
776
ARG004 Argyria 26 0.107
777
MTR087 Maternal Uniparental Disomy 28 0.107
778
DWR001 Dwarfism 44 0.107
779
XLN235 X-Linked Intellectual Disability with Marfanoid Habitus 29 0.107
780
SMN008 Semantic Dementia 46 0.107
781
SPL018 Splenomegaly 47 0.107
782
P DYS021 Dysautonomia 38 0.107
783
P CRB088 Cerebral Atrophy 32 0.107
784
CRB090 Cerebral Hypoxia 42 0.107
785
c HRD088 Hereditary Neuropathies 34 0.107
786
BLN017 Balint Syndrome 17 0.107
787
P OVR082 Overgrowth Syndrome 41 0.107
788
c PRM340 Primary Adrenal Insufficiency 37 0.107
Content
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