Search results for Fluoxetine

542 hits were found for Fluoxetine

# Family MCID Name MIFTS Score
1
END040 Endogenous Depression 53 0.172
2
SRT004 Serotonin Syndrome 49 0.172
3
MNT002 Mental Depression 53 0.167
4
MDD011 Mood Disorder 61 0.142
5
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.139
6
DRG001 Drug Psychosis 38 0.125
7
OBS002 Obsessive-Compulsive Disorder 66 0.121
8
PRM003 Premature Ejaculation 45 0.121
9
c MJR008 Major Affective Disorder 2 19 0.121
10
c MJR003 Major Affective Disorder 6 15 0.121
11
DSS008 Disease of Mental Health 52 0.111
12
c MJR007 Major Affective Disorder 1 24 0.111
13
TRC010 Trichotillomania 40 0.108
14
GNR004 Generalized Anxiety Disorder 51 0.100
15
c MJR006 Major Affective Disorder 5 15 0.097
16
ANX002 Anxiety Disorder 67 0.092
17
CND002 Conduct Disorder 54 0.088
18
PSY004 Psychotic Disorder 67 0.079
19
ATS001 Autistic Disorder 63 0.079
20
CRB039 Cerebrovascular Disease 63 0.079
21
P PRS038 Personality Disorder 62 0.079
22
ISC004 Ischemia 61 0.079
23
P PNC025 Panic Disorder 60 0.079
24
SBS003 Substance Abuse 54 0.079
25
DRG003 Drug Dependence 50 0.079
26
BDY001 Body Dysmorphic Disorder 39 0.079
27
c MJR004 Major Affective Disorder 4 16 0.079
28
STR067 Stroke, Ischemic 75 0.074
29
P ALC004 Alcohol Abuse 59 0.074
30
PRV006 Pervasive Developmental Disorder 53 0.074
31
CCN001 Cocaine Dependence 49 0.074
32
SBS004 Substance Dependence 47 0.074
33
OBS003 Obsessive-Compulsive Personality Disorder 36 0.074
34
MLN003 Melancholia 34 0.074
35
P OBS005 Obesity 92 0.068
36
P EPL164 Epilepsy 66 0.068
37
BLM002 Bulimia Nervosa 52 0.068
38
ATN002 Autonomic Nervous System Disease 48 0.068
39
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.068
40
BRN080 Brain Ischemia 41 0.068
41
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.068
42
ALC007 Alcohol Dependence 63 0.062
43
MTH009 Mouth Disease 61 0.062
44
P ENC018 Encephalopathy 59 0.062
45
PST028 Post-Traumatic Stress Disorder 57 0.062
46
P CNG001 Congenital Myasthenic Syndrome 55 0.062
47
ADL002 Adult Syndrome 52 0.062
48
P SPS003 Spastic Diplegia 52 0.062
49
MVM001 Movement Disease 49 0.062
50
SCL003 Social Phobia 46 0.062
51
PRM020 Premenstrual Tension 44 0.062
52
MTS001 Mutism 43 0.062
53
SPC010 Speech and Communication Disorders 41 0.062
54
NRN002 Neuronitis 41 0.062
55
ADJ001 Adjustment Disorder 38 0.062
56
WTH001 Withdrawal Disorder 37 0.062
57
DYS009 Dysthymic Disorder 37 0.062
58
NTR005 Nutritional Deficiency Disease 36 0.062
59
c PNC070 Panic Disorder 2 14 0.062
60
P BPL003 Bipolar Disorder 62 0.056
61
ETN001 Eating Disorder 58 0.056
62
P SZR006 Seizure Disorder 56 0.056
63
GST023 Gastric Ulcer 56 0.056
64
PRP019 Peripheral Nervous System Disease 55 0.056
65
c PND001 Pain Disorder 54 0.056
66
BRN071 Brain Injury 52 0.056
67
CCN002 Cocaine Abuse 48 0.056
68
c BPL002 Bipolar I Disorder 47 0.056
69
ALN001 Aland Island Eye Disease 45 0.056
70
INT025 Intermittent Explosive Disorder 38 0.056
71
DPR002 Depersonalization Disorder 35 0.056
72
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 33 0.056
73
c PNC068 Panic Disorder 3 15 0.056
74
P RSP003 Respiratory Failure 71 0.048
75
P LYM118 Lymphoma 69 0.048
76
PCK002 Pick Disease 68 0.048
77
CNT098 Central Core Disease 65 0.048
78
P ANR007 Anorexia Nervosa 61 0.048
79
c CNT035 Central Nervous System Disease 60 0.048
80
RSP006 Respiratory System Disease 58 0.048
81
CHL071 Child Syndrome 58 0.048
82
EXF001 Exfoliation Syndrome 57 0.048
83
FCL014 Focal Epilepsy 55 0.048
84
KDS001 Kid Syndrome 53 0.048
85
SLP005 Sleep Disorder 53 0.048
86
TRM010 Traumatic Brain Injury 52 0.048
87
SMT006 Somatoform Disorder 50 0.048
88
LRN003 Learning Disability 49 0.048
89
NCT008 Nicotine Dependence, Protection Against 49 0.048
90
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.048
91
CRB085 Cerebral Hemorrhage 46 0.048
92
P PLN008 Peeling Skin Syndrome 45 0.048
93
ACR041 Acromelic Frontonasal Dysostosis 45 0.048
94
BRT030 Birth Defects 43 0.048
95
SXL003 Sexual Disorder 42 0.048
96
SMT001 Somatization Disorder 42 0.048
97
PRD011 Proud Syndrome 42 0.048
98
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.048
99
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.048
100
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.048
101
ACT084 Acute Stress Disorder 40 0.048
102
c PLN018 Peeling Skin Syndrome 2 40 0.048
103
ADR009 Adrenal Cortex Disease 39 0.048
104
PST055 Postural Hypotension 36 0.048
105
ALC003 Alcoholic Psychosis 33 0.048
106
c PLN021 Peeling Skin Syndrome 3 29 0.048
107
P CRN178 Coronary Heart Disease 6 21 0.048
108
CYT018 Cytochrome P450 2d6 Variant 19 0.048
109
P LNG032 Lung Cancer 95 0.039
110
P OST012 Osteoarthritis 83 0.039
111
P HNT016 Huntington Disease 80 0.039
112
P PLM037 Pulmonary Hypertension 79 0.039
113
P SCH015 Schizophrenia 77 0.039
114
P HRT032 Heart Disease 75 0.039
115
MLT021 Multiple System Atrophy 70 0.039
116
P PRK057 Parkinson Disease, Late-Onset 70 0.039
117
BRN028 Brain Cancer 70 0.039
118
SQM006 Squamous Cell Carcinoma 70 0.039
119
P ADN016 Adenocarcinoma 69 0.039
120
c HYP595 Hypertension, Essential 69 0.039
121
P MYP004 Myopathy 67 0.039
122
VSC007 Vascular Disease 67 0.039
123
P KDN018 Kidney Disease 66 0.039
124
OBS061 Obstructive Sleep Apnea 66 0.039
125
c CHR089 Chronic Kidney Failure 66 0.039
126
DWN001 Down Syndrome 66 0.039
127
ATH003 Atherosclerosis 65 0.039
128
DMN002 Dementia 65 0.039
129
P PLR004 Pleuropulmonary Blastoma 65 0.039
130
HMT002 Hematologic Cancer 64 0.039
131
P ALX003 Alexander Disease 63 0.039
132
P LNG064 Lung Cancer Susceptibility 3 62 0.039
133
GST092 Gastroesophageal Reflux 62 0.039
134
APH001 Aphthous Stomatitis 62 0.039
135
GLL008 Gilles De La Tourette Syndrome 62 0.039
136
P SLP006 Sleep Apnea 61 0.039
137
HYP056 Hypoglycemia 61 0.039
138
P ANG001 Angelman Syndrome 61 0.039
139
P ESP024 Esophagitis 61 0.039
140
P IDP010 Idiopathic Generalized Epilepsy 61 0.039
141
HYP020 Hyperprolactinemia 60 0.039
142
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.039
143
WLL006 Wells Syndrome 59 0.039
144
P HYP060 Hyperinsulinism 58 0.039
145
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.039
146
CTS003 Coats Disease 57 0.039
147
ORL015 Oral Squamous Cell Carcinoma 57 0.039
148
c ACT210 Acute Respiratory Distress Syndrome 57 0.039
149
P HMR003 Hemorrhagic Disease 57 0.039
150
HRP004 Herpes Zoster 56 0.039
151
NRM005 Neuromuscular Disease 56 0.039
152
P SML001 Small Cell Carcinoma 56 0.039
153
HYP266 Hypoxia 56 0.039
154
GST050 Gastrointestinal System Disease 56 0.039
155
END030 End Stage Renal Failure 55 0.039
156
P MMB011 Membranous Nephropathy 54 0.039
157
LNG039 Lung Squamous Cell Carcinoma 54 0.039
158
ESP023 Esophageal Disease 54 0.039
159
SML033 Small Cell Cancer of the Lung, Somatic 54 0.039
160
RTN018 Retinal Disease 53 0.039
161
HMR039 Hemorrhage, Intracerebral 53 0.039
162
PRT058 Pure Autonomic Failure 52 0.039
163
P MSC033 Muscle Disorders 52 0.039
164
BRN038 Bronchial Disease 51 0.039
165
ADN009 Adenosquamous Carcinoma 51 0.039
166
DRG011 Drug Addiction 51 0.039
167
c LRG001 Large Cell Carcinoma 51 0.039
168
STM006 Stomach Disease 50 0.039
169
BNF002 Bone Fracture 50 0.039
170
OPT003 Opiate Dependence 50 0.039
171
URN009 Urinary System Disease 50 0.039
172
OVR063 Overnutrition 50 0.039
173
P URF003 Urofacial Syndrome 1 50 0.039
174
BRX001 Bruxism 49 0.039
175
PST021 Postpartum Depression 49 0.039
176
ATN005 Autonomic Dysfunction 49 0.039
177
RTN003 Retinal Ischemia 48 0.039
178
DYS073 Dysphagia 48 0.039
179
RTN020 Retinal Vascular Disease 48 0.039
180
GYN001 Gynecomastia 48 0.039
181
BRD004 Borderline Personality Disorder 47 0.039
182
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.039
183
BLD053 Blood Platelet Disease 46 0.039
184
GLT021 Glutaricaciduria, Type I 46 0.039
185
ADN027 Adenomyosis 46 0.039
186
CRB090 Cerebral Hypoxia 45 0.039
187
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 0.039
188
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.039
189
GDS001 Good Syndrome 44 0.039
190
P BRN120 Bronchus Cancer 44 0.039
191
P DYS021 Dysautonomia 44 0.039
192
c CNT015 Central Sleep Apnea 44 0.039
193
ANX004 Anoxia 43 0.039
194
ACT058 Active Peptic Ulcer Disease 43 0.039
195
P CRB088 Cerebral Atrophy 42 0.039
196
NRL004 Neuroleptic Malignant Syndrome 41 0.039
197
ADN010 Adenosquamous Cell Lung Carcinoma 41 0.039
198
SPC005 Speech Disorder 41 0.039
199
OPD001 Opioid Abuse 40 0.039
200
CNN002 Cannabis Abuse 40 0.039
201
GST078 Gastrointestinal Allergy 40 0.039
202
BSL008 Basal Ganglia Disease 40 0.039
203
NRT001 Neurotic Disorder 40 0.039
204
IMP006 Impulse Control Disorder 40 0.039
205
CRB009 Cerebritis 39 0.039
206
MYF002 Myofascial Pain Syndrome 39 0.039
207
HYP540 Hypertension, Diastolic 39 0.039
208
P FML187 Familial Hypertension 38 0.039
209
P LNG035 Lung Large Cell Carcinoma 38 0.039
210
c PRK030 Parkinson Disease 4 38 0.039
211
HYP016 Hypochondriasis 38 0.039
212
CNN001 Cannabis Dependence 38 0.039
213
OCL011 Ocular Motility Disease 37 0.039
214
c MLT010 Multiple Personality Disorder 36 0.039
215
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.039
216
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 35 0.039
217
c PLM022 Pulmonary Valve Insufficiency 34 0.039
218
PHB001 Phobic Disorder 34 0.039
219
c PLN017 Peeling Skin Syndrome 1 34 0.039
220
IMP003 Impaired Renal Function Disease 34 0.039
221
ANG049 Angioedema Induced by Ace Inhibitors 34 0.039
222
SWL001 Swallowing Disorders 33 0.039
223
FNC006 Functional Gastric Disease 32 0.039
224
GLB003 Globe Disease 32 0.039
225
CRB040 Cerebrum Cancer 32 0.039
226
P ACT080 Acute Pulmonary Heart Disease 31 0.039
227
c CNT068 Central Pain Syndrome 29 0.039
228
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.039
229
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.039
230
VSL004 Visual Cortex Disease 28 0.039
231
DYS011 Dyskinesia of Esophagus 28 0.039
232
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.039
233
c SCH051 Schizophrenia 4 28 0.039
234
c ANR038 Anorexia Nervosa 1 26 0.039
235
YNG002 Young Syndrome 26 0.039
236
c CRN214 Coronary Heart Disease 5 22 0.039
237
MND006 Mondor Disease 21 0.039
238
CMB002 Combat Disorder 21 0.039
239
c CRN177 Coronary Heart Disease 7 20 0.039
240
P GNR027 Generalized Peeling Skin Syndrome 19 0.039
241
c SCH064 Schizophrenia 10 19 0.039
242
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.039
243
PRM227 Primary Orthostatic Hypotension 18 0.039
244
c ATS173 Autism 18 17 0.039
245
ELC001 Elective Mutism 17 0.039
246
c DYS033 Dysautonomia Like Disorder 16 0.039
247
c ATS171 Autism 9 16 0.039
248
c SML023 Small Cell Lung Cancer, Adult 15 0.039
249
BRN017 Bronchogenic Lung Adenocarcinoma 13 0.039
250
MLT076 Multiple System Atrophy with Orthostatic Hypotension 10 0.039
251
THN007 Thinking Seizures 9 0.039
252
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.028
253
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.028
254
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.028
255
P RTT002 Rett Syndrome 77 0.028
256
P ART022 Arthritis 75 0.028
257
CRH001 Crohn's Disease 75 0.028
258
INS024 Insulin-Like Growth Factor I 75 0.028
259
P CRN211 Coronary Artery Disease 74 0.028
260
P WSK001 Wiskott-Aldrich Syndrome 73 0.028
261
CNG034 Congestive Heart Failure 72 0.028
262
P NRV007 Nervous System Disease 71 0.028
263
P NRB001 Neuroblastoma 70 0.028
264
BRK010 Burkitt Lymphoma 69 0.028
265
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.028
266
P DRV001 Dravet Syndrome 69 0.028
267
PRP027 Peripheral Vascular Disease 68 0.028
268
ISC006 Ischemic Heart Disease 68 0.028
269
P MNN013 Meningitis 67 0.028
270
SKN016 Skin Disease 66 0.028
271
URN008 Urinary Bladder Cancer 66 0.028
272
BRC012 Brucellosis 66 0.028
273
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.028
274
P ATS007 Autism Spectrum Disorder 65 0.028
275
P BCL006 B-Cell Lymphomas 65 0.028
276
P DYS154 Dystonia 65 0.028
277
P AGM001 Agammaglobulinemia 64 0.028
278
P LNG028 Long Qt Syndrome 64 0.028
279
LNG099 Lung Disease 64 0.028
280
CHR066 Chronic Fatigue Syndrome 64 0.028
281
P PRD008 Periodontitis 63 0.028
282
P MCH002 Machado-Joseph Disease 63 0.028
283
P FML161 Familial Mediterranean Fever, Ar 63 0.028
284
P ENC004 Encephalitis 63 0.028
285
SPN186 Spinal Cord Injury 63 0.028
286
LPT001 Leptospirosis 62 0.028
287
P PRD006 Prader-Willi Syndrome 62 0.028
288
P SDD001 Sudden Infant Death Syndrome 61 0.028
289
CRB011 Cerebrotendinous Xanthomatosis 61 0.028
290
P DNT015 Dent Disease 61 0.028
291
P NRV006 Nervous System Cancer 60 0.028
292
P GST049 Gastrointestinal System Cancer 60 0.028
293
PRM097 Primary Immunodeficiency Disease 60 0.028
294
PRD007 Periodontal Disease 60 0.028
295
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
296
P ORL007 Oral Cavity Cancer 59 0.028
297
OCL009 Ocular Cancer 59 0.028
298
P NTR004 Neutropenia 59 0.028
299
P NRP001 Neuropathy 59 0.028
300
P INF032 Infertility 59 0.028
301
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.028
302
P PRP029 Porphyria 59 0.028
303
LPD008 Lipid Metabolism Disorder 58 0.028
304
MTR014 Motor Neuron Disease 58 0.028
305
RHM027 Rheumatic Disease 58 0.028
306
PPT005 Peptic Ulcer Disease 58 0.028
307
P CND004 Candidiasis 57 0.028
308
GST033 Gestational Diabetes 57 0.028
309
c PRC016 Pre-Eclampsia 56 0.028
310
ORL011 Oral Cancer 56 0.028
311
TRN015 Transient Cerebral Ischemia 56 0.028
312
PRS047 Prostatitis 56 0.028
313
ART111 Artery Disease 55 0.028
314
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.028
315
GLC003 Glucose Intolerance 55 0.028
316
MLN007 Male Infertility 55 0.028
317
P HYP097 Hyperekplexia 54 0.028
318
P HYP083 Hypopituitarism 54 0.028
319
APH002 Aphasia 54 0.028
320
CHN016 Cohen Syndrome 54 0.028
321
VSC002 Vascular Dementia 54 0.028
322
P MCR129 Microvascular Complications of Diabetes 1 54 0.028
323
PTT046 Pituitary Hormone Deficiency, Combined, 2 54 0.028
324
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.028
325
NWC001 Newcastle Disease 54 0.028
326
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.028
327
P ECL001 Eclampsia 54 0.028
328
DMY004 Demyelinating Disease 53 0.028
329
FDL002 Food Allergy 53 0.028
330
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.028
331
P NNT009 Neonatal Diabetes Mellitus 52 0.028
332
ISL003 Isolated Growth Hormone Deficiency 52 0.028
333
P ANG015 Angioedema 52 0.028
334
MRG003 Marginal Zone B-Cell Lymphoma 52 0.028
335
c OPT055 Optic Atrophy Plus Syndrome 52 0.028
336
OPT006 Optic Nerve Disease 52 0.028
337
CRC006 Carcinoid Syndrome 52 0.028
338
c PRK031 Parkinson Disease 1 51 0.028
339
BLD044 Bladder Disease 51 0.028
340
ART002 Arts Syndrome 51 0.028
341
MYL001 Myelitis 51 0.028
342
P PRC031 Preeclampsia/eclampsia 1 51 0.028
343
HMP005 Hemiplegia 51 0.028
344
CRN030 Coronary Stenosis 51 0.028
345
GRW007 Growth Hormone Deficiency 50 0.028
346
AMN001 Amenorrhea 50 0.028
347
NNT012 Neonatal Jaundice 50 0.028
348
P CHR345 Chronic Pain 50 0.028
349
P CLL015 Collagen Disease 50 0.028
350
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.028
351
HLL004 Hellp Syndrome 50 0.028
352
CSY001 C Syndrome 50 0.028
353
TMP001 Temporal Lobe Epilepsy 50 0.028
354
P SCK002 Sick Sinus Syndrome 50 0.028
355
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.028
356
c SVR005 Severe Pre-Eclampsia 49 0.028
357
c ACT071 Acute Kidney Failure 49 0.028
358
c INH020 Inherited Metabolic Disorder 49 0.028
359
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.028
360
LPD004 Lipoid Nephrosis 48 0.028
361
ORL005 Oral Candidiasis 48 0.028
362
P MYT002 Myotonic Dystrophy 48 0.028
363
TCD001 Tic Disorder 48 0.028
364
FML039 Female Reproductive System Disease 48 0.028
365
P TRC086 Trichohepatoenteric Syndrome 1 48 0.028
366
c HMG001 Hemoglobin C Disease 47 0.028
367
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.028
368
PTT009 Pituitary Gland Disease 47 0.028
369
CRB027 Cerebellar Disease 47 0.028
370
DWR001 Dwarfism 47 0.028
371
AMN002 Amino Acid Metabolic Disorder 47 0.028
372
BRD001 Brody Myopathy 47 0.028
373
CRB025 Carbohydrate Metabolic Disorder 46 0.028
374
PRP021 Peripheral Nervous System Neoplasm 46 0.028
375
HRT007 Heart Cancer 46 0.028
376
P CRN035 Cranial Nerve Palsy 46 0.028
377
P PRM108 Primary Progressive Multiple Sclerosis 46 0.028
378
XNT003 Xanthomatosis 46 0.028
379
PRP007 Priapism 46 0.028
380
HDN002 Head Injury 45 0.028
381
P CRV039 Cervicitis 45 0.028
382
VSC047 Vascular Malformation 45 0.028
383
ATN004 Autonomic Neuropathy 45 0.028
384
ACD009 Acid-Labile Subunit, Deficiency of 45 0.028
385
CCN007 Cocoon Syndrome 45 0.028
386
MXD023 Mixed Cell Type Cancer 44 0.028
387
CHR056 Chronic Tic Disorder 44 0.028
388
HYP085 Hypothalamic Disease 44 0.028
389
BWN001 Bowen-Conradi Syndrome 44 0.028
390
c MTR002 Mitral Valve Insufficiency 44 0.028
391
c HMG003 Hemoglobin E Disease 44 0.028
392
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.028
393
PHY002 Physical Disorder 43 0.028
394
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.028
395
SKN027 Skin Conditions 43 0.028
396
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.028
397
P BLP003 Blepharospasm 43 0.028
398
c OPT053 Optic Atrophy 1 43 0.028
399
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.028
400
BCK006 Back Pain 43 0.028
401
BHR001 Behr Syndrome 42 0.028
402
GLC008 Glucose Metabolism Disease 42 0.028
403
VGN023 Vaginitis 42 0.028
404
BLR008 Bilirubin Metabolic Disorder 42 0.028
405
MYC033 Myoclonus 42 0.028
406
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.028
407
PNM013 Pneumococcal Meningitis 41 0.028
408
PHC013 Phaeochromocytoma 41 0.028
409
AYM001 Ayme-Gripp Syndrome 41 0.028
410
RPR002 Reproductive System Disease 41 0.028
411
CHR413 Chronic Myocardial Ischemia 41 0.028
412
CNV002 Conversion Disorder 41 0.028
413
RMS001 Rem Sleep Behavior Disorder 41 0.028
414
c PRK045 Parkinson Disease 5 40 0.028
415
P HYP263 Hypersomnia 40 0.028
416
ADT003 Auditory System Disease 40 0.028
417
c CHR096 Chronic Pulmonary Heart Disease 40 0.028
418
MNN017 Mononeuropathy 40 0.028
419
CRN031 Cranial Nerve Disease 40 0.028
420
BND014 Bone Development Disease 40 0.028
421
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.028
422
ATN003 Autonomic Nervous System Neoplasm 40 0.028
423
GRW004 Growth Retardation with Deafness and Mental Retardation Due to Igf1 Deficiency 39 0.028
424
BRS064 Bursitis 39 0.028
425
HYP030 Hypoactive Sexual Desire Disorder 39 0.028
426
c PCH012 Pachyonychia Congenita 2 38 0.028
427
P HYP265 Hypotonia 38 0.028
428
SCT001 Sciatic Neuropathy 38 0.028
429
KLP001 Kleptomania 38 0.028
430
SPC003 Specific Developmental Disorder 38 0.028
431
P OCY001 Oocyte Maturation Defect 38 0.028
432
P UTR038 Uterine Disease 37 0.028
433
BLD054 Blood Protein Disease 37 0.028
434
PRP080 Peripheral Artery Disease 37 0.028
435
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 37 0.028
436
CMB021 Combined Pituitary Hormone Deficiency 37 0.028
437
NSY001 N Syndrome 36 0.028
438
OPT008 Optic Nerve Neoplasm 36 0.028
439
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.028
440
ATM014 Autoimmune Disease of Endocrine System 36 0.028
441
ALR002 Al-Raqad Syndrome 36 0.028
442
LMB010 Lambert Syndrome 36 0.028
443
ATM012 Autoimmune Disease of Blood 35 0.028
444
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.028
445
MSC004 Muscle Tissue Disease 34 0.028
446
RDN001 Reading Disorder 34 0.028
447
RMN001 Rumination Disorder 34 0.028
448
DPN001 Dependent Personality Disorder 34 0.028
449
MLR007 Male Reproductive System Disease 34 0.028
450
PLS010 Plasma Protein Metabolism Disease 34 0.028
451
ACR002 Acrocapitofemoral Dysplasia 33 0.028
452
PLC008 Placenta Disease 33 0.028
453
SPR012 Separation Anxiety Disorder 33 0.028
454
CRB159 Cerebral Visual Impairment 33 0.028
455
P MYS047 Myasthenic Syndrome, Congenital, 1b, Fast-Channel 33 0.028
456
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.028
457
c DNT021 Dent Disease 2 33 0.028
458
ATY001 Atypical Depressive Disorder 32 0.028
459
DSS010 Dissociative Disorder 32 0.028
460
P HRT017 Heart Tumor 32 0.028
461
DRG004 Drug-Induced Mental Disorder 31 0.028
462
FST001 Foster-Kennedy Syndrome 31 0.028
463
ORM002 Oromandibular Dystonia 31 0.028
464
PRG092 Pregnancy Loss, Recurrent 1 31 0.028
465
c HMG004 Hemoglobin D Disease 31 0.028
466
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 30 0.028
467
PRG090 Progressive Relapsing Multiple Sclerosis 30 0.028
468
c PRK051 Parkinson Disease 18 30 0.028
469
PDP001 Pedophilia 30 0.028
470
PTT045 Pituitary Hormone Deficiency, Combined, 1 30 0.028
471
BRW006 Brown Syndrome 29 0.028
472
EXH001 Exhibitionism 29 0.028
473
C9D001 C9 Deficiency 29 0.028
474
c TRC078 Trichohepatoenteric Syndrome 2 29 0.028
475
P PRM016 Primary Optic Atrophy 29 0.028
476
TRN006 Transvestism 29 0.028
477
PSD088 Pseudobulbar Affect 28 0.028
478
MDN002 Median Neuropathy 28 0.028
479
CRB031 Cerebral Arterial Disease 27 0.028
480
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.028
481
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.028
482
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 26 0.028
483
FTS001 Fetishism 26 0.028
484
NTR042 Neutrophilic Dermatosis, Acute Febrile 25 0.028
485
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.028
486
c WSK002 Wiskott-Aldrich Syndrome 2 25 0.028
487
c PCH010 Pachyonychia Congenita 3 25 0.028
488
c ATM007 Autoimmune Disease of Central Nervous System 25 0.028
489
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.028
490
c OPT023 Optic Atrophy 2 25 0.028
491
ATM052 Autoimmune Disease 1 25 0.028
492
PST103 Postpartum Psychosis 25 0.028
493
SBC016 Subacute Delirium 24 0.028
494
HRY002 Hairy Tongue 24 0.028
495
EYC003 Eye Accommodation Disease 24 0.028
496
c MLT124 Multiple Sclerosis 5 23 0.028
497
c SCH056 Schizophrenia 15 23 0.028
498
INS009 Insulin-Resistance Type B 22 0.028
499
c MYS046 Myasthenic Syndrome, Congenital, 1a, Slow-Channel 22 0.028
500
BRR004 Baroreflex Failure 22 0.028
501
c MYS059 Myasthenic Syndrome, Congenital, 4a, Slow-Channel 22 0.028
502
ATM059 Autoimmune Disease 6 22 0.028
503
PRG096 Pregnancy Loss, Recurrent 2 21 0.028
504
VYR001 Voyeurism 21 0.028
505
c CRN174 Coronary Heart Disease 2 20 0.028
506
c OPT025 Optic Atrophy 6 20 0.028
507
c MYS062 Myasthenic Syndrome, Congenital, 2a, Slow-Channel 20 0.028
508
PTT043 Pituitary Hormone Deficiency, Combined, 6 19 0.028
509
c CRN175 Coronary Heart Disease 4 19 0.028
510
c CRN172 Coronary Heart Disease 3 19 0.028
511
VSC009 Vascular Skin Disease 19 0.028
512
c MYS060 Myasthenic Syndrome, Congenital, 4b, Fast-Channel 19 0.028
513
c MYS049 Myasthenic Syndrome, Congenital, 3b, Fast-Channel 18 0.028
514
c CRN173 Coronary Heart Disease 8 18 0.028
515
c MYS048 Myasthenic Syndrome, Congenital, 3a, Slow-Channel 18 0.028
516
c MLT093 Multiple Sclerosis 2 18 0.028
517
c CRN176 Coronary Heart Disease 9 18 0.028
518
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.028
519
BLC017 Black Hairy Tongue 18 0.028
520
ATN001 Autonomic Peripheral Neuropathy 17 0.028
521
c OPT024 Optic Atrophy 5 17 0.028
522
c OPT059 Optic Atrophy 4 17 0.028
523
c ADL079 Adult Heart Tumor 16 0.028
524
c PRC032 Preeclampsia/eclampsia 2 16 0.028
525
c MLT095 Multiple Sclerosis 4 16 0.028
526
ATM053 Autoimmune Disease 2 16 0.028
527
ATM054 Autoimmune Disease 3 15 0.028
528
ATM055 Autoimmune Disease 4 15 0.028
529
CGT001 Ciguatera Fish Poisoning 15 0.028
530
c ATS172 Autism 10 15 0.028
531
CD4004 Cd4 Deficiency 14 0.028
532
INH003 Inhibited Female Orgasm 14 0.028
533
MLG026 Male Genital Organ Vascular Disease 14 0.028
534
CYP013 Cyp2c19-Related Poor Drug Metabolism 14 0.028
535
CRT056 Carotidynia 14 0.028
536
P CYP006 Cyp2c19-Related Altered Drug Metabolism 14 0.028
537
ORG003 Organic Mood Syndrome 13 0.028
538
EXT011 Extrapyramidal and Movement Disease 13 0.028
539
c SPR097 Sporadic Hyperekplexia 12 0.028
540
c CYP009 Cyp2d6-Related Altered Drug Metabolism 11 0.028
541
ACT231 Acute Flaccid Myelitis 10 0.028
542
LWM001 Low Implantation of Placenta 8 0.028
Content
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