Search results for Risperidone

554 hits were found for Risperidone

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 77 0.473
2
DRG001 Drug Psychosis 38 0.364
3
PSY004 Psychotic Disorder 67 0.357
4
DSS008 Disease of Mental Health 52 0.357
5
c SCH051 Schizophrenia 4 28 0.266
6
SRT004 Serotonin Syndrome 49 0.229
7
EXF001 Exfoliation Syndrome 57 0.214
8
P PLN008 Peeling Skin Syndrome 45 0.214
9
HYP020 Hyperprolactinemia 60 0.197
10
P GNR027 Generalized Peeling Skin Syndrome 19 0.185
11
P BPL003 Bipolar Disorder 62 0.183
12
ATS001 Autistic Disorder 63 0.172
13
c PLN021 Peeling Skin Syndrome 3 29 0.168
14
MTH009 Mouth Disease 61 0.166
15
MDD011 Mood Disorder 61 0.166
16
c PLN018 Peeling Skin Syndrome 2 40 0.166
17
CND002 Conduct Disorder 54 0.159
18
NRL004 Neuroleptic Malignant Syndrome 41 0.156
19
c BPL002 Bipolar I Disorder 47 0.151
20
TRD006 Tardive Dyskinesia 49 0.141
21
ATN002 Autonomic Nervous System Disease 48 0.135
22
PRP007 Priapism 46 0.132
23
CSY001 C Syndrome 50 0.126
24
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.123
25
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.123
26
DLS001 Delusional Disorder 41 0.120
27
c SCH064 Schizophrenia 10 19 0.120
28
PRV006 Pervasive Developmental Disorder 53 0.117
29
PHY002 Physical Disorder 43 0.117
30
DMN002 Dementia 65 0.114
31
P SHR029 Short Syndrome 58 0.114
32
c PLN017 Peeling Skin Syndrome 1 34 0.114
33
ANX002 Anxiety Disorder 67 0.107
34
END040 Endogenous Depression 53 0.107
35
MNT002 Mental Depression 53 0.107
36
SCH003 Schizophreniform Disorder 40 0.103
37
P ATS007 Autism Spectrum Disorder 65 0.100
38
GNR004 Generalized Anxiety Disorder 51 0.100
39
WTH001 Withdrawal Disorder 37 0.100
40
PRP019 Peripheral Nervous System Disease 55 0.096
41
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.096
42
MVM001 Movement Disease 49 0.096
43
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.096
44
ADJ001 Adjustment Disorder 38 0.096
45
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.096
46
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.092
47
P PRS038 Personality Disorder 62 0.092
48
SBS003 Substance Abuse 54 0.092
49
GLC025 Galactorrhoea-Hyperprolactinaemia 18 0.087
50
c SCH061 Schizophrenia 16 16 0.087
51
CHL071 Child Syndrome 58 0.083
52
KDS001 Kid Syndrome 53 0.083
53
DRG003 Drug Dependence 50 0.083
54
NTR005 Nutritional Deficiency Disease 36 0.083
55
LRN003 Learning Disability 49 0.078
56
CCN001 Cocaine Dependence 49 0.078
57
SXL003 Sexual Disorder 42 0.078
58
NSY001 N Syndrome 36 0.078
59
MSC004 Muscle Tissue Disease 34 0.078
60
P ALZ034 Alzheimer Disease 92 0.073
61
P MYP004 Myopathy 67 0.073
62
WLL006 Wells Syndrome 59 0.073
63
P MSC033 Muscle Disorders 52 0.073
64
P SPS003 Spastic Diplegia 52 0.073
65
SBS004 Substance Dependence 47 0.073
66
GDS001 Good Syndrome 44 0.073
67
ACT084 Acute Stress Disorder 40 0.073
68
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.073
69
PCK002 Pick Disease 68 0.068
70
OBS002 Obsessive-Compulsive Disorder 66 0.068
71
PST028 Post-Traumatic Stress Disorder 57 0.068
72
P INT063 Intellectual Disability 49 0.068
73
CCN002 Cocaine Abuse 48 0.068
74
GYN001 Gynecomastia 48 0.068
75
PRN009 Paranoid Schizophrenia 47 0.068
76
OPP004 Oppositional Defiant Disorder 43 0.068
77
c SCH056 Schizophrenia 15 23 0.068
78
c MJR008 Major Affective Disorder 2 19 0.068
79
c MJR003 Major Affective Disorder 6 15 0.068
80
EXT011 Extrapyramidal and Movement Disease 13 0.068
81
GLL008 Gilles De La Tourette Syndrome 62 0.062
82
P PNC025 Panic Disorder 60 0.062
83
c CNT035 Central Nervous System Disease 60 0.062
84
SLP005 Sleep Disorder 53 0.062
85
PTT009 Pituitary Gland Disease 47 0.062
86
c ERL020 Early-Onset Schizophrenia 47 0.062
87
ALN001 Aland Island Eye Disease 45 0.062
88
HYP085 Hypothalamic Disease 44 0.062
89
HYP070 Hyperpituitarism 38 0.062
90
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.062
91
SCH011 Schizotypal Personality Disorder 33 0.062
92
ATY001 Atypical Depressive Disorder 32 0.062
93
GRN016 Grant Syndrome 29 0.062
94
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.062
95
c SCH059 Schizophrenia 17 26 0.062
96
YNG002 Young Syndrome 26 0.062
97
c MJR007 Major Affective Disorder 1 24 0.062
98
c MJR004 Major Affective Disorder 4 16 0.062
99
P OBS005 Obesity 92 0.055
100
P DYS154 Dystonia 65 0.055
101
CNT098 Central Core Disease 65 0.055
102
CRB039 Cerebrovascular Disease 63 0.055
103
ALC007 Alcohol Dependence 63 0.055
104
P ALC004 Alcohol Abuse 59 0.055
105
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.055
106
ART021 Arteriosclerosis 58 0.055
107
VSC002 Vascular Dementia 54 0.055
108
ADL002 Adult Syndrome 52 0.055
109
AMN001 Amenorrhea 50 0.055
110
BRD004 Borderline Personality Disorder 47 0.055
111
GLT021 Glutaricaciduria, Type I 46 0.055
112
CRB004 Cerebral Artery Occlusion 45 0.055
113
ACR041 Acromelic Frontonasal Dysostosis 45 0.055
114
SKN023 Skin Tag 44 0.055
115
BRT030 Birth Defects 43 0.055
116
PRD011 Proud Syndrome 42 0.055
117
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.055
118
TRC010 Trichotillomania 40 0.055
119
SXD001 Sex Differentiation Disease 38 0.055
120
ATY003 Atypical Autism 29 0.055
121
CRB031 Cerebral Arterial Disease 27 0.055
122
DRG016 Drug Induced Dyskinesia 23 0.055
123
CRB087 Cerebral Arteriosclerosis 21 0.055
124
INT074 Intracranial Arteriosclerosis 14 0.055
125
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.048
126
P HNT016 Huntington Disease 80 0.048
127
P HYP086 Hypothyroidism 64 0.048
128
P ALX003 Alexander Disease 63 0.048
129
LPD008 Lipid Metabolism Disorder 58 0.048
130
ETN001 Eating Disorder 58 0.048
131
c PND001 Pain Disorder 54 0.048
132
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.048
133
DRG011 Drug Addiction 51 0.048
134
ASP001 Asperger Syndrome 50 0.048
135
P CHR345 Chronic Pain 50 0.048
136
ATN005 Autonomic Dysfunction 49 0.048
137
LPD004 Lipoid Nephrosis 48 0.048
138
TCD001 Tic Disorder 48 0.048
139
CRB025 Carbohydrate Metabolic Disorder 46 0.048
140
GLC008 Glucose Metabolism Disease 42 0.048
141
SPC005 Speech Disorder 41 0.048
142
ADT003 Auditory System Disease 40 0.048
143
BSL008 Basal Ganglia Disease 40 0.048
144
c MLT010 Multiple Personality Disorder 36 0.048
145
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.048
146
AMP007 Amphetamine Abuse 35 0.048
147
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.048
148
CHL012 Childhood Disintegrative Disease 35 0.048
149
RDN001 Reading Disorder 34 0.048
150
ANG049 Angioedema Induced by Ace Inhibitors 34 0.048
151
c TRC078 Trichohepatoenteric Syndrome 2 29 0.048
152
SBC016 Subacute Delirium 24 0.048
153
EYC003 Eye Accommodation Disease 24 0.048
154
c CRN175 Coronary Heart Disease 4 19 0.048
155
WSC001 Wisconsin Syndrome 14 0.048
156
c PNC070 Panic Disorder 2 14 0.048
157
NVS004 Nova Syndrome 13 0.048
158
P OST012 Osteoarthritis 83 0.039
159
P MYC007 Myocardial Infarction 79 0.039
160
P RTT002 Rett Syndrome 77 0.039
161
P HRT032 Heart Disease 75 0.039
162
P NRV007 Nervous System Disease 71 0.039
163
P HPT021 Hepatitis 69 0.039
164
P PNM007 Pneumonia 68 0.039
165
P EPL164 Epilepsy 66 0.039
166
P LNG028 Long Qt Syndrome 64 0.039
167
ISC004 Ischemia 61 0.039
168
HYP066 Hyperglycemia 61 0.039
169
P ANR007 Anorexia Nervosa 61 0.039
170
RBR001 Roberts Syndrome 60 0.039
171
P NTR004 Neutropenia 59 0.039
172
STT001 Status Epilepticus 59 0.039
173
P HYP060 Hyperinsulinism 58 0.039
174
P EXN002 Exanthem 57 0.039
175
VRL011 Viral Infectious Disease 55 0.039
176
ERY003 Erythema Multiforme 55 0.039
177
P MCR129 Microvascular Complications of Diabetes 1 54 0.039
178
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.039
179
NWC001 Newcastle Disease 54 0.039
180
PLN006 Poland Syndrome 54 0.039
181
P THY097 Thyroid Hormone Resistance 54 0.039
182
C3D001 C3 Deficiency 53 0.039
183
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.039
184
ALL026 Allergic Hypersensitivity Disease 52 0.039
185
TXC002 Toxic Encephalopathy 51 0.039
186
PTH002 Pathological Gambling 51 0.039
187
IMM136 Immune System Disease 51 0.039
188
P CRP007 Carpenter Syndrome 51 0.039
189
MST005 Mastitis 51 0.039
190
RTN023 Retinitis 50 0.039
191
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.039
192
LPD009 Lipid Storage Disease 49 0.039
193
THY030 Thyroid Gland Disease 48 0.039
194
P GNR032 Generalized Dystonia 45 0.039
195
ACD009 Acid-Labile Subunit, Deficiency of 45 0.039
196
CHR056 Chronic Tic Disorder 44 0.039
197
OCL069 Ocular Motor Apraxia 44 0.039
198
c MTR002 Mitral Valve Insufficiency 44 0.039
199
P DYS021 Dysautonomia 44 0.039
200
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.039
201
P BLP003 Blepharospasm 43 0.039
202
MLT001 Multiple Chemical Sensitivity 43 0.039
203
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.039
204
SPC010 Speech and Communication Disorders 41 0.039
205
RPR002 Reproductive System Disease 41 0.039
206
NRN002 Neuronitis 41 0.039
207
IMP006 Impulse Control Disorder 40 0.039
208
ACT088 Acute Insulin Response 39 0.039
209
INT025 Intermittent Explosive Disorder 38 0.039
210
KNZ001 Kanzaki Disease 38 0.039
211
SPC003 Specific Developmental Disorder 38 0.039
212
OCL011 Ocular Motility Disease 37 0.039
213
OBS003 Obsessive-Compulsive Personality Disorder 36 0.039
214
DVL001 Developmental Coordination Disorder 36 0.039
215
MLN003 Melancholia 34 0.039
216
P XLN007 X-Linked Disease 34 0.039
217
SWL001 Swallowing Disorders 33 0.039
218
P ATS049 Autism Susceptibility, X-Linked 2 33 0.039
219
DSS010 Dissociative Disorder 32 0.039
220
DRG004 Drug-Induced Mental Disorder 31 0.039
221
c CRP022 Carpenter Syndrome 2 31 0.039
222
c OST147 Osteoarthritis 1 30 0.039
223
c MNT149 Mental Retardation, X-Linked 3 29 0.039
224
WRT002 Writing Disorder 27 0.039
225
c ANR038 Anorexia Nervosa 1 26 0.039
226
GRN033 Granulomatous Mastitis 25 0.039
227
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.039
228
c CRN214 Coronary Heart Disease 5 22 0.039
229
P CRN178 Coronary Heart Disease 6 21 0.039
230
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.039
231
c CRN173 Coronary Heart Disease 8 18 0.039
232
c DYS137 Dystonia 4 18 0.039
233
c DYS033 Dysautonomia Like Disorder 16 0.039
234
c ATS171 Autism 9 16 0.039
235
PRP074 Peripheral Resistance to Thyroid Hormones 16 0.039
236
c MJR006 Major Affective Disorder 5 15 0.039
237
c PNC068 Panic Disorder 3 15 0.039
238
THY021 Thyroid Malformation 11 0.039
239
P LNG032 Lung Cancer 95 0.028
240
P PLM037 Pulmonary Hypertension 79 0.028
241
STR067 Stroke, Ischemic 75 0.028
242
WLS001 Wilson Disease 72 0.028
243
PHN003 Phenylketonuria 72 0.028
244
P INF038 Influenza 72 0.028
245
P RSP003 Respiratory Failure 71 0.028
246
P PRK057 Parkinson Disease, Late-Onset 70 0.028
247
BRN028 Brain Cancer 70 0.028
248
P ADN016 Adenocarcinoma 69 0.028
249
P FRG001 Fragile X Syndrome 69 0.028
250
PRP027 Peripheral Vascular Disease 68 0.028
251
P MNN013 Meningitis 67 0.028
252
P KDN018 Kidney Disease 66 0.028
253
OBS061 Obstructive Sleep Apnea 66 0.028
254
BRC012 Brucellosis 66 0.028
255
DWN001 Down Syndrome 66 0.028
256
ACR007 Acromegaly 66 0.028
257
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.028
258
P HRP006 Herpes Simplex 65 0.028
259
PTR006 Peters Anomaly 65 0.028
260
P PLR004 Pleuropulmonary Blastoma 65 0.028
261
P ENC004 Encephalitis 63 0.028
262
P LNG064 Lung Cancer Susceptibility 3 62 0.028
263
P VLC001 Velocardiofacial Syndrome 62 0.028
264
GST092 Gastroesophageal Reflux 62 0.028
265
APH001 Aphthous Stomatitis 62 0.028
266
GLC037 Glucocorticoid Resistance 62 0.028
267
P PRD006 Prader-Willi Syndrome 62 0.028
268
c LNG044 Long Qt Syndrome 1 62 0.028
269
P SLP006 Sleep Apnea 61 0.028
270
LSC001 Lesch-Nyhan Syndrome 61 0.028
271
P IDP010 Idiopathic Generalized Epilepsy 61 0.028
272
CRD119 Cardiac Arrest 61 0.028
273
P HYP117 Hypertriglyceridemia 61 0.028
274
c ACT075 Acute Myocardial Infarction 60 0.028
275
P MCP010 Mucopolysaccharidosis 60 0.028
276
PLM033 Pulmonary Embolism 60 0.028
277
P NRV006 Nervous System Cancer 60 0.028
278
WLL001 Williams-Beuren Syndrome 60 0.028
279
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
280
GLB001 Gilbert Syndrome 60 0.028
281
P NRN021 Neuronal Ceroid Lipofuscinosis 59 0.028
282
P HMN010 Hemangioma 59 0.028
283
OCL009 Ocular Cancer 59 0.028
284
P ENC018 Encephalopathy 59 0.028
285
MRB003 Morbid Obesity 58 0.028
286
PNC034 Pancreas Disease 58 0.028
287
c LNG047 Long Qt Syndrome 2 57 0.028
288
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.028
289
ABL002 Ablepharon-Macrostomia Syndrome 57 0.028
290
ART017 Aortic Disease 57 0.028
291
ADR005 Adrenal Carcinoma 57 0.028
292
THR024 Thrombosis 57 0.028
293
MSC077 Muscle Eye Brain Disease 57 0.028
294
SNS001 Sensorineural Hearing Loss 57 0.028
295
WST001 West Syndrome 57 0.028
296
STR026 Star Syndrome 57 0.028
297
P SZR006 Seizure Disorder 56 0.028
298
NRM005 Neuromuscular Disease 56 0.028
299
WLF001 Wolff-Parkinson-White Syndrome 56 0.028
300
LYM027 Lymphopenia 56 0.028
301
PRR007 Perry Syndrome 55 0.028
302
GLC003 Glucose Intolerance 55 0.028
303
P TRM003 Tremor 54 0.028
304
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.028
305
HDC001 Headache 54 0.028
306
c BCT007 Bacterial Meningitis 54 0.028
307
P MMB011 Membranous Nephropathy 54 0.028
308
CHN016 Cohen Syndrome 54 0.028
309
ESP023 Esophageal Disease 54 0.028
310
PLM010 Pulmonary Edema 54 0.028
311
RST001 Restless Legs Syndrome 54 0.028
312
c ART101 Aortic Valve Disease 2 53 0.028
313
AGN012 Agnathia-Otocephaly Complex 53 0.028
314
P HYP024 Hypoparathyroidism 53 0.028
315
SCT005 Scott Syndrome 53 0.028
316
c EPL070 Epilepsy, Progressive Myoclonic 2b 53 0.028
317
RTN018 Retinal Disease 53 0.028
318
P DGR001 Digeorge Syndrome 53 0.028
319
P CYS018 Cystitis 52 0.028
320
TTH006 Tooth Disease 52 0.028
321
BRN106 Burns 52 0.028
322
BRN004 Brain Edema 52 0.028
323
P ANG015 Angioedema 52 0.028
324
CYT008 Cytomegalovirus Infection 52 0.028
325
c ALZ037 Alzheimer Disease-2 52 0.028
326
LYM024 Lymphatic System Disease 52 0.028
327
OPT006 Optic Nerve Disease 52 0.028
328
MYC002 Mycobacterium Avium Complex Disease 52 0.028
329
SMT008 Smith-Magenis Syndrome 52 0.028
330
PHL006 Phelan-Mcdermid Syndrome 51 0.028
331
BRN038 Bronchial Disease 51 0.028
332
ART002 Arts Syndrome 51 0.028
333
P ESN008 Eosinophilic Pneumonia 51 0.028
334
P CPL006 Capillary Hemangioma 51 0.028
335
VSC006 Vascular Cancer 51 0.028
336
HYP005 Hypokalemia 51 0.028
337
c LNG050 Long Qt Syndrome 5 51 0.028
338
CRN030 Coronary Stenosis 51 0.028
339
P PLY017 Polyarteritis Nodosa 51 0.028
340
c ART115 Aortic Valve Disease 1 50 0.028
341
c VRL012 Viral Meningitis 50 0.028
342
SMT006 Somatoform Disorder 50 0.028
343
c ACT068 Acute Cystitis 50 0.028
344
OPT003 Opiate Dependence 50 0.028
345
INT075 Intracranial Hypertension 50 0.028
346
ANG054 Angina Pectoris 50 0.028
347
END035 Endocrine Gland Cancer 49 0.028
348
c LNG051 Long Qt Syndrome 6 49 0.028
349
RTN015 Retinal Cancer 49 0.028
350
MSC072 Muscle Cancer 49 0.028
351
SPR099 Supravalvar Aortic Stenosis 49 0.028
352
c INH020 Inherited Metabolic Disorder 49 0.028
353
P KBK002 Kabuki Syndrome 1 49 0.028
354
c LNG092 Long Qt Syndrome-3 49 0.028
355
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.028
356
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.028
357
P FML035 Familial Hyperlipidemia 48 0.028
358
c EPL099 Epileptic Encephalopathy, Early Infantile, 15 48 0.028
359
QBC001 Quebec Platelet Disorder 48 0.028
360
ADR012 Adrenal Gland Disease 48 0.028
361
RTN003 Retinal Ischemia 48 0.028
362
OCL006 Ocular Hypertension 48 0.028
363
PLS009 Plasma Cell Neoplasm 48 0.028
364
MSS002 Mass Syndrome 48 0.028
365
CRN017 Coronary Thrombosis 48 0.028
366
P CMP008 Compartment Syndrome 48 0.028
367
DYS073 Dysphagia 48 0.028
368
SLP001 Sleeping Sickness 48 0.028
369
P TRC086 Trichohepatoenteric Syndrome 1 48 0.028
370
RTN020 Retinal Vascular Disease 48 0.028
371
CYT005 Cytomegalovirus Retinitis 47 0.028
372
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.028
373
VND001 Vein Disease 47 0.028
374
PRT030 Parathyroid Gland Disease 47 0.028
375
ANT011 Antisocial Personality Disorder 47 0.028
376
MGR028 Migraine with or Without Aura 1 47 0.028
377
AMN002 Amino Acid Metabolic Disorder 47 0.028
378
BRD001 Brody Myopathy 47 0.028
379
PRP021 Peripheral Nervous System Neoplasm 46 0.028
380
HRT007 Heart Cancer 46 0.028
381
BLD053 Blood Platelet Disease 46 0.028
382
ADR038 Adermatoglyphia 46 0.028
383
P INF016 Infantile Epileptic Encephalopathy 46 0.028
384
SCL003 Social Phobia 46 0.028
385
INC022 Inclusion-Cell Disease 46 0.028
386
MGC001 Megacolon 45 0.028
387
HDN002 Head Injury 45 0.028
388
PTT037 Pituitary Tumors 45 0.028
389
VSC047 Vascular Malformation 45 0.028
390
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.028
391
VTM002 Vitamin B12 Deficiency 44 0.028
392
c SHR030 Short Qt Syndrome 44 0.028
393
CRD118 Cardiovascular Cancer 44 0.028
394
P BRN120 Bronchus Cancer 44 0.028
395
c LNG053 Long Qt Syndrome 9 44 0.028
396
BNN003 Bone Inflammation Disease 44 0.028
397
c LNG096 Long Qt Syndrome 15 44 0.028
398
PHR002 Pharyngoconjunctival Fever 44 0.028
399
P RTN014 Retinal Artery Occlusion 44 0.028
400
c CNT015 Central Sleep Apnea 44 0.028
401
PRM020 Premenstrual Tension 44 0.028
402
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.028
403
MTS001 Mutism 43 0.028
404
AMN003 Amnestic Disorder 43 0.028
405
LKC003 Leukocyte Disease 43 0.028
406
P MGS004 Meige Syndrome 43 0.028
407
SNS023 Sensory System Cancer 43 0.028
408
PRD004 Prediabetes Syndrome 43 0.028
409
BHR001 Behr Syndrome 42 0.028
410
NRR001 Neuroretinitis 42 0.028
411
SMT001 Somatization Disorder 42 0.028
412
c VRL005 Viral Pneumonia 42 0.028
413
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.028
414
PRM025 Primary Bacterial Infectious Disease 41 0.028
415
BRN080 Brain Ischemia 41 0.028
416
NRS003 Neurosyphilis 41 0.028
417
P CNG390 Congenital Pulmonary Airway Malformation 41 0.028
418
CNV002 Conversion Disorder 41 0.028
419
c HMN027 Hemangioma, Capillary Infantile 41 0.028
420
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.028
421
CNN002 Cannabis Abuse 40 0.028
422
HRT012 Heart Valve Disease 40 0.028
423
GST078 Gastrointestinal Allergy 40 0.028
424
DRG002 Drug-Induced Hepatitis 40 0.028
425
MNC019 Monocarboxylate Transporter 1 Deficiency 40 0.028
426
P ARC016 Auriculocondylar Syndrome 1 40 0.028
427
BND014 Bone Development Disease 40 0.028
428
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.028
429
ATN003 Autonomic Nervous System Neoplasm 40 0.028
430
LYM127 Lymphatic Malformations 39 0.028
431
SKL003 Skeletal Muscle Cancer 39 0.028
432
SPN369 Spinal Disease 39 0.028
433
SKN018 Skin Hemangioma 39 0.028
434
ADR009 Adrenal Cortex Disease 39 0.028
435
BDY001 Body Dysmorphic Disorder 39 0.028
436
P HYP265 Hypotonia 38 0.028
437
ABR009 Abruzzo-Erickson Syndrome 38 0.028
438
c EPL037 Epileptic Encephalopathy, Early Infantile, 1 38 0.028
439
BRN026 Branch Retinal Artery Occlusion 38 0.028
440
c PRK030 Parkinson Disease 4 38 0.028
441
CNN001 Cannabis Dependence 38 0.028
442
CDS002 Codas Syndrome 37 0.028
443
PRP080 Peripheral Artery Disease 37 0.028
444
c PNC106 Pancreatic Agenesis 1 37 0.028
445
HYP189 Hypoadrenalism 37 0.028
446
c CNG031 Congenital Nervous System Abnormality 37 0.028
447
PRL008 Paralytic Ileus 37 0.028
448
CNG069 Congenital Cytomegalovirus 36 0.028
449
MDY003 Mody, Type Ii 36 0.028
450
CPL005 Capillary Disease 36 0.028
451
ISC005 Ischemic Bone Disease 36 0.028
452
P CRB154 Cerebrocostomandibular Syndrome 36 0.028
453
ADR010 Adrenal Cortical Hypofunction 36 0.028
454
ALR002 Al-Raqad Syndrome 36 0.028
455
LMB010 Lambert Syndrome 36 0.028
456
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.028
457
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.028
458
MTL002 Metal Metabolism Disorder 35 0.028
459
CHL078 Childhood-Onset Schizophrenia 34 0.028
460
c EPL025 Epileptic Encephalopathy, Early Infantile, 2 34 0.028
461
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.028
462
PLS010 Plasma Protein Metabolism Disease 34 0.028
463
c CNG007 Congenital Adrenal Insufficiency 34 0.028
464
ACR002 Acrocapitofemoral Dysplasia 33 0.028
465
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.028
466
MRK002 Marek Disease 33 0.028
467
LNS003 Lens Disease 33 0.028
468
ACD004 Acdc 33 0.028
469
HMR023 Hemorrhagic Cystitis 33 0.028
470
KHL003 Kohlschutter-Tonz Syndrome 32 0.028
471
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 32 0.028
472
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 32 0.028
473
P HRT017 Heart Tumor 32 0.028
474
P CHR084 Chromosomal Disease 32 0.028
475
PST086 Posterior Cortical Atrophy 32 0.028
476
WSM002 Waisman Syndrome 32 0.028
477
FST001 Foster-Kennedy Syndrome 31 0.028
478
c HMG004 Hemoglobin D Disease 31 0.028
479
CYT004 Cytomegalic Inclusion Disease 31 0.028
480
JNS003 Jensen Syndrome 31 0.028
481
PDT040 Pediatric Hypertension 30 0.028
482
PDP001 Pedophilia 30 0.028
483
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.028
484
SPS016 Spasmodic Dysphonia 29 0.028
485
CYL001 Cayler Cardiofacial Syndrome 29 0.028
486
c CNT068 Central Pain Syndrome 29 0.028
487
C9D001 C9 Deficiency 29 0.028
488
HMN011 Hemangioma of Intra-Abdominal Structure 29 0.028
489
PRM243 Primary Bone Cancer 29 0.028
490
VSL004 Visual Cortex Disease 28 0.028
491
DYS011 Dyskinesia of Esophagus 28 0.028
492
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.028
493
NNT021 Neonatal Meningitis 28 0.028
494
WRF003 Warfarin Syndrome 28 0.028
495
c CHR565 Chromosomal Deletion Syndrome 27 0.028
496
c SHR033 Short Qt Syndrome 3 27 0.028
497
c SHR032 Short Qt Syndrome 2 27 0.028
498
c ALZ014 Alzheimer Disease 16 27 0.028
499
c SHR031 Short Qt Syndrome 1 27 0.028
500
c KBK003 Kabuki Syndrome 2 27 0.028
501
CNT023 Central Nervous System Hemangioma 26 0.028
502
NNT018 Neonatal Herpes 26 0.028
503
c EPL127 Epileptic Encephalopathy, Early Infantile, 21 25 0.028
504
HMN012 Hemangioma of Lung 25 0.028
505
CRB014 Cerebral Angioma 24 0.028
506
P MJR018 Major Affective Disorder-7 24 0.028
507
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 24 0.028
508
KHL001 Kohler's Disease 24 0.028
509
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 23 0.028
510
NRS005 Neurosarcoidosis 23 0.028
511
PLM124 Pulmonary Hypertension, Neonatal 22 0.028
512
c DYS186 Dystonia 2 22 0.028
513
ISC009 Ischemic Retinopathy 21 0.028
514
BRN123 Branchial Arch Syndrome, X-Linked 21 0.028
515
BRN027 Brain Angioma 21 0.028
516
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.028
517
c CRN174 Coronary Heart Disease 2 20 0.028
518
CNG489 Congenital Herpes Simplex Virus Infection 20 0.028
519
HYP611 Hypoparathyroidism, X-Linked 20 0.028
520
c CRN177 Coronary Heart Disease 7 20 0.028
521
CYT018 Cytochrome P450 2d6 Variant 19 0.028
522
c CRN172 Coronary Heart Disease 3 19 0.028
523
VSC009 Vascular Skin Disease 19 0.028
524
MNT257 Mental Retardation, X-Linked, with Craniofacial Dysmorphism 18 0.028
525
c CRN176 Coronary Heart Disease 9 18 0.028
526
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.028
527
c ATS173 Autism 18 17 0.028
528
c ADL079 Adult Heart Tumor 16 0.028
529
c CNG100 Congenital Herpes Simplex 16 0.028
530
MLT131 Multifocal Atrial Tachycardia 16 0.028
531
GLC077 Glucocorticoid Therapy, Response to 16 0.028
532
c CNG396 Congenital Pulmonary Airway Malformation Type 2 15 0.028
533
CHR235 Chromosome 22q Deletion 15 0.028
534
WHT007 White Platelet Syndrome 15 0.028
535
HRT029 Heart Tumor of the Child 15 0.028
536
c ATS172 Autism 10 15 0.028
537
c CNG398 Congenital Pulmonary Airway Malformation Type 1 14 0.028
538
NVD002 Nevada Syndrome 14 0.028
539
CYP013 Cyp2c19-Related Poor Drug Metabolism 14 0.028
540
P CYP006 Cyp2c19-Related Altered Drug Metabolism 14 0.028
541
BRN017 Bronchogenic Lung Adenocarcinoma 13 0.028
542
c SPS018 Spastic Diplegia Infantile Type 13 0.028
543
c DLT001 Delta Chain Disease 13 0.028
544
STR005 Stork Bite 13 0.028
545
c GNR024 Generalized Peeling Skin Syndrome Type C 12 0.028
546
BDS001 Bd Syndrome 12 0.028
547
RTN189 Retinal Capillary Malformation 12 0.028
548
NNT002 Neonatal Urinary Tract Infectious Disease 11 0.028
549
c CYP009 Cyp2d6-Related Altered Drug Metabolism 11 0.028
550
TSY001 Tau Syndrome 10 0.028
551
MNT033 Mental Retardation X-Linked Dysmorphism 10 0.028
552
BNJ001 Benjamin Syndrome 9 0.028
553
ART033 Aortic Valves Stenosis of the Child 9 0.028
554
ATS014 Autism with Port-Wine Stain 8 0.028
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