Search results for Citalopram

615 hits were found for Citalopram

# Family MCID Name MIFTS Score
1
P MJR001 Major Depressive Disorder 68 29.935
2
MNT002 Mental Depression 56 18.167
3
DPR016 Depression 64 17.050
4
END040 Endogenous Depression 54 9.663
5
NRT001 Neurotic Disorder 56 7.802
6
OBS002 Obsessive-Compulsive Disorder 67 6.947
7
ANX010 Anxiety 70 5.400
8
ALC007 Alcohol Dependence 65 5.370
9
P PNC025 Panic Disorder 52 5.326
10
P SCH015 Schizophrenia 74 4.895
11
P ALZ034 Alzheimer Disease 87 4.852
12
P DMN002 Dementia 65 4.798
13
P PRS038 Personality Disorder 65 4.670
14
P ALC033 Alcohol Use Disorder 67 4.665
15
SRT004 Serotonin Syndrome 54 4.642
16
P BPL003 Bipolar Disorder 56 4.639
17
c MJR022 Major Affective Disorder 8 37 4.632
18
c MJR024 Major Affective Disorder 9 40 4.632
19
c ATS007 Autism Spectrum Disorder 71 4.411
20
MDD011 Mood Disorder 61 4.351
21
P ATS364 Autism 72 4.053
22
P PRV006 Pervasive Developmental Disorder 52 4.050
23
SXL003 Sexual Disorder 49 3.988
24
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.971
25
P TRM003 Tremor 50 3.945
26
PSY004 Psychotic Disorder 66 3.887
27
SCL003 Social Phobia 48 3.646
28
PST028 Post-Traumatic Stress Disorder 58 3.559
29
IRR002 Irritable Bowel Syndrome 64 3.509
30
LPP008 Lipoprotein Quantitative Trait Locus 65 3.491
31
STR067 Stroke, Ischemic 79 3.343
32
P PRK039 Parkinsonism 55 3.275
33
TRM010 Traumatic Brain Injury 50 3.223
34
BRN071 Brain Injury 50 3.187
35
P PRK057 Parkinson Disease, Late-Onset 79 3.183
36
GNR004 Generalized Anxiety Disorder 54 3.026
37
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.003
38
c HPT001 Hepatitis C 61 3.003
39
AVD001 Avoidant Personality Disorder 49 2.947
40
P SZR006 Seizure Disorder 69 2.884
41
MLD017 Mal De Debarquement Syndrome 33 2.884
42
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.844
43
DSS008 Disease of Mental Health 74 2.729
44
BRD004 Borderline Personality Disorder 53 2.695
45
PRM003 Premature Ejaculation 44 2.614
46
MLN003 Melancholia 41 2.605
47
P MJR007 Major Affective Disorder 1 42 2.542
48
GST092 Gastroesophageal Reflux 59 2.514
49
DYS009 Dysthymic Disorder 51 2.467
50
MLD018 Mild Cognitive Impairment 48 2.456
51
CCN002 Cocaine Abuse 49 2.451
52
ANT039 Antisynthetase Syndrome 55 2.442
53
P LNG028 Long Qt Syndrome 63 2.416
54
P HPT021 Hepatitis 68 2.415
55
AGR002 Agoraphobia 45 2.387
56
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 2.371
57
CCN001 Cocaine Dependence 47 2.371
58
P BRS047 Breast Cancer 97 2.368
59
CRD132 Cardiac Conduction Defect 59 2.354
60
FRN006 Frontotemporal Dementia 68 2.343
61
CNS004 Constipation 56 2.299
62
ETN001 Eating Disorder 59 2.290
63
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.272
64
ALL029 Allergic Disease 61 2.247
65
c MJR008 Major Affective Disorder 2 34 2.236
66
c MJR006 Major Affective Disorder 5 32 2.236
67
c MJR023 Major Affective Disorder 7 33 2.236
68
c MJR004 Major Affective Disorder 4 28 2.236
69
c MJR003 Major Affective Disorder 6 32 2.236
70
P TRN020 Turner Syndrome 67 2.236
71
FBR047 Fibromyalgia 57 2.185
72
AND005 Androgen Insensitivity Syndrome, Mild 21 2.174
73
ART140 Arteries, Anomalies of 52 2.164
74
INP001 Inappropriate Adh Syndrome 48 2.149
75
P KHL003 Kohlschutter-Tonz Syndrome 57 2.127
76
VSC002 Vascular Dementia 59 2.124
77
P SBS003 Substance Abuse 54 2.119
78
P CHR345 Chronic Pain 50 2.104
79
P CRD119 Cardiac Arrest 68 2.072
80
P HNT016 Huntington Disease 73 2.007
81
SCH003 Schizophreniform Disorder 54 1.967
82
P ESP024 Esophagitis 60 1.962
83
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.954
84
SMT001 Somatization Disorder 49 1.954
85
SMT006 Somatoform Disorder 50 1.934
86
PST021 Postpartum Depression 50 1.896
87
OCL069 Ocular Motor Apraxia 57 1.874
88
PRM020 Premenstrual Tension 39 1.872
89
P SHR001 Short Bowel Syndrome 53 1.871
90
OPD001 Opioid Abuse 44 1.859
91
ACT084 Acute Stress Disorder 53 1.854
92
ISC004 Ischemia 61 1.839
93
OPD006 Opioid Addiction 48 1.835
94
P SLP005 Sleep Disorder 61 1.795
95
CHR066 Chronic Fatigue Syndrome 59 1.787
96
OBS003 Obsessive-Compulsive Personality Disorder 43 1.776
97
CYT002 Cytokine Deficiency 43 1.770
98
P EXN002 Exanthem 58 1.768
99
GLM045 Glioma 62 1.750
100
GLL048 Glial Tumor 51 1.750
101
RHB024 Rhabdomyosarcoma 2 65 1.723
102
HNT002 Hantavirus Pulmonary Syndrome 55 1.723
103
APH002 Aphasia 55 1.713
104
P MYC007 Myocardial Infarction 69 1.713
105
HYP005 Hypokalemia 55 1.704
106
CRB039 Cerebrovascular Disease 65 1.681
107
SYN036 Syncope 44 1.654
108
P TMP001 Temporal Lobe Epilepsy 49 1.653
109
P HRT032 Heart Disease 84 1.646
110
P KDN018 Kidney Disease 71 1.645
111
P MYC033 Myoclonus 46 1.643
112
c MGR028 Migraine with or Without Aura 1 63 1.638
113
ANR007 Anorexia Nervosa 59 1.594
114
P RHM011 Rheumatoid Arthritis 81 1.586
115
ACR006 Aceruloplasminemia 63 1.577
116
P ATX024 Ataxia-Oculomotor Apraxia 3 46 1.577
117
P FRD001 Friedreich Ataxia 62 1.577
118
c HPT003 Hepatitis a 63 1.577
119
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.577
120
P HDC001 Headache 56 1.555
121
P LVR013 Liver Disease 68 1.532
122
ATN005 Autonomic Dysfunction 45 1.512
123
P ENC018 Encephalopathy 62 1.497
124
PNG002 Pain Agnosia 51 1.495
125
P EPL164 Epilepsy 70 1.488
126
DBT010 Diabetic Neuropathy 54 1.484
127
HPT019 Hepatic Encephalopathy 59 1.465
128
HPT004 Hepatic Coma 43 1.465
129
SCH012 Schizoaffective Disorder 49 1.457
130
IMP005 Impotence 52 1.452
131
P MVM001 Movement Disease 61 1.452
132
NRL004 Neuroleptic Malignant Syndrome 52 1.430
133
CRB004 Cerebral Artery Occlusion 45 1.412
134
SVR004 Severe Combined Immunodeficiency 70 1.399
135
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.387
136
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.387
137
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 1.387
138
CGN007 Cognitive Function 1, Social 27 1.387
139
URT001 Urethritis 52 1.387
140
NTR005 Nutritional Deficiency Disease 60 1.387
141
NRD001 Neurodermatitis 39 1.387
142
P CRD246 Cardiovascular System Disease 55 1.387
143
CHL079 Children's Interstitial Lung Disease 25 1.387
144
PRR013 Prurigo Nodularis 38 1.387
145
P TCD001 Tic Disorder 50 1.370
146
48X005 48,xyyy 39 1.361
147
WTH001 Withdrawal Disorder 47 1.345
148
P PLM037 Pulmonary Hypertension 69 1.345
149
P VSC007 Vascular Disease 62 1.345
150
BLM002 Bulimia Nervosa 56 1.322
151
CRD223 Cardiac Arrhythmia 63 1.305
152
P DYS154 Dystonia 64 1.295
153
P HPT023 Hepatocellular Carcinoma 95 1.294
154
IMP006 Impulse Control Disorder 44 1.294
155
PTH003 Pathologic Nystagmus 52 1.287
156
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.275
157
PRT058 Pure Autonomic Failure 58 1.270
158
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.268
159
P MCH002 Machado-Joseph Disease 62 1.257
160
SBC016 Subacute Delirium 42 1.257
161
BDY001 Body Dysmorphic Disorder 40 1.255
162
ATY001 Atypical Depressive Disorder 45 1.255
163
ACQ007 Acquired Immunodeficiency Syndrome 58 1.255
164
AMN001 Amenorrhea 53 1.249
165
PRP080 Peripheral Artery Disease 54 1.234
166
SPN186 Spinal Cord Injury 60 1.234
167
PRP007 Priapism 46 1.227
168
c PNS012 Paine Syndrome 60 1.221
169
47X002 47,xyy 47 1.185
170
P AST005 Asthma 75 1.161
171
HMN044 Human Immunodeficiency Virus Type 1 76 1.159
172
PTH002 Pathological Gambling 48 1.153
173
DPN001 Dependent Personality Disorder 26 1.153
174
HND015 Hand Skill, Relative 29 1.136
175
AGN016 Aging 53 1.128
176
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.118
177
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.118
178
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.118
179
P ALP008 Alopecia 53 1.118
180
P ASP001 Asperger Syndrome 48 1.099
181
P CRN037 Craniosynostosis 67 1.099
182
TRN015 Transient Cerebral Ischemia 62 1.099
183
P NRC002 Narcolepsy 55 1.099
184
P NRB001 Neuroblastoma 66 1.099
185
TRD006 Tardive Dyskinesia 53 1.080
186
STT001 Status Epilepticus 58 1.080
187
SPS057 Spasticity 43 1.080
188
GLC096 Galactorrhea 40 1.058
189
TRC010 Trichotillomania 51 1.058
190
P MLT020 Multiple Sclerosis 79 1.055
191
ADL002 Adult Syndrome 69 1.044
192
OPT003 Opiate Dependence 49 1.044
193
P CLR023 Colorectal Cancer 100 1.044
194
PSD088 Pseudobulbar Affect 33 1.044
195
CHR105 Choreoacanthocytosis 55 1.037
196
OST003 Osteonecrosis 60 0.984
197
P OST002 Osteoporosis 76 0.970
198
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.970
199
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.970
200
c ACT071 Acute Kidney Failure 60 0.970
201
CHR073 Choreatic Disease 53 0.970
202
TMP019 Temporomandibular Joint Anomaly 28 0.970
203
c LKM061 Leukemia, Acute Myeloid 83 0.953
204
P RST001 Restless Legs Syndrome 52 0.949
205
P RSP003 Respiratory Failure 73 0.933
206
c FNC043 Fanconi Anemia, Complementation Group E 62 0.929
207
CHR682 Chronic Bilirubin Encephalopathy 37 0.929
208
P DRR001 Diarrhea 55 0.927
209
DYS073 Dysphagia 53 0.916
210
P HYP263 Hypersomnia 40 0.916
211
LVR012 Liver Cirrhosis 62 0.916
212
DPR002 Depersonalization Disorder 41 0.916
213
P RHN004 Rhinitis 56 0.898
214
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.898
215
P SNS001 Sensorineural Hearing Loss 60 0.859
216
P THR014 Thrombocytopenia 66 0.859
217
c BNM021 Bone Mineral Density Quantitative Trait Locus 7 12 0.854
219
DWN001 Down Syndrome 70 0.854
220
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.854
221
P ANR048 Aniridia 1 66 0.854
222
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 0.854
223
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.854
224
PCK003 Pick Disease of Brain 70 0.854
225
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.854
226
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 64 0.854
227
PST048 Postural Orthostatic Tachycardia Syndrome 46 0.854
228
MYF002 Myofascial Pain Syndrome 46 0.854
229
CRB009 Cerebritis 43 0.854
230
P ART022 Arthritis 70 0.854
231
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.854
233
WHP002 Whiplash 35 0.854
234
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.838
235
PHY002 Physical Disorder 40 0.838
236
c ESS001 Essential Tremor 56 0.838
237
MLT116 Multiple System Atrophy, Parkinsonian Type 29 0.838
238
PRS063 Paresthesia 39 0.838
239
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.815
240
PRS129 Prostatic Hyperplasia, Benign 48 0.815
241
PHR003 Pharyngitis 57 0.815
242
P INT068 Intestinal Disease 53 0.815
243
HMP005 Hemiplegia 53 0.815
244
PRS021 Prostatic Adenoma 43 0.815
245
PRS045 Prostatic Hypertrophy 53 0.815
246
BNG077 Benign Idiopathic Neonatal Seizures 23 0.815
247
MTB004 Metabolic Acidosis 48 0.791
248
ATM095 Autoimmune Disease 61 0.791
249
P ACT028 Acute Closed-Angle Glaucoma 32 0.791
250
BRX001 Bruxism 50 0.791
251
P ADL010 Adult Respiratory Distress Syndrome 70 0.791
252
CRT015 Carotid Artery Occlusion 45 0.791
253
P DYS021 Dysautonomia 38 0.791
254
P CTN003 Cutaneous Lupus Erythematosus 52 0.763
255
c SCH079 Schizophrenia 1 44 0.763
256
IMM167 Immune Deficiency Disease 76 0.763
257
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.763
258
INT025 Intermittent Explosive Disorder 39 0.763
259
P MYP006 Myopia 55 0.763
260
P MGR001 Migraine Without Aura 48 0.763
261
PRM013 Premature Menopause 57 0.763
262
ALL014 Allergic Encephalomyelitis 34 0.763
263
NNT008 Neonatal Abstinence Syndrome 41 0.763
264
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.763
265
ANS006 Anosognosia 34 0.732
266
HYP457 Hypertrophic Scars 42 0.732
267
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.732
268
OST017 Osteomyelitis 63 0.732
269
INT067 Interstitial Nephritis 46 0.732
270
P ATN002 Autonomic Nervous System Disease 51 0.732
271
P MYP004 Myopathy 67 0.732
272
HYP016 Hypochondriasis 47 0.732
273
HYP264 Hypertonia 35 0.732
274
ATR057 Atrioventricular Block 54 0.696
275
P HYP750 Hypertriglyceridemia, Familial 61 0.696
276
c PNC122 Panic Disorder 1 19 0.696
277
SPP007 Suppression Amblyopia 38 0.696
278
ANT011 Antisocial Personality Disorder 47 0.696
279
NRT004 Neuritis 53 0.696
280
AMB002 Amblyopia 49 0.696
281
MCL006 Macular Retinal Edema 56 0.696
282
P PNM007 Pneumonia 64 0.696
283
CRN019 Coronary Artery Vasospasm 47 0.696
284
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.696
285
OLV001 Olivopontocerebellar Atrophy 50 0.696
286
P MYL006 Myeloid Leukemia 60 0.696
287
VSL012 Visual Snow Syndrome 18 0.696
288
P CRB059 Cerebellar Degeneration 36 0.696
289
P ALP009 Alopecia Areata 59 0.696
290
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.696
291
P HYP265 Hypotonia 42 0.696
292
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.655
293
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.648
294
STT041 Stuttering 52 0.648
295
WLF002 Wolf-Hirschhorn Syndrome 57 0.648
296
INF021 Infant Gynecomastia 30 0.648
297
GYN001 Gynecomastia 48 0.648
298
P MCR010 Microcephaly 59 0.648
299
LFT001 Left Bundle Branch Hemiblock 47 0.648
300
P LCT001 Lactic Acidosis 50 0.648
301
c FML191 Familial Long Qt Syndrome 54 0.648
302
P CRN300 Coronary Heart Disease 1 73 0.628
303
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.597
304
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.597
305
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.597
306
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.597
307
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.597
308
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.597
309
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.597
310
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.597
311
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.597
312
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.597
313
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.597
314
P LTR001 Lateral Sclerosis 57 0.597
315
c HPT073 Hepatitis C Virus 70 0.560
316
GLB002 Glioblastoma 67 0.560
317
CNG034 Congestive Heart Failure 69 0.560
318
c BPL002 Bipolar I Disorder 47 0.560
320
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.532
321
ANS021 Anisocoria 24 0.532
322
NNL006 Non-Alcoholic Steatohepatitis 54 0.532
323
P MGR003 Migraine with Aura 51 0.532
324
P RTN022 Retinal Vein Occlusion 54 0.532
325
MLT001 Multiple Chemical Sensitivity 38 0.532
326
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.532
327
BRC012 Brucellosis 66 0.532
328
CNT016 Central Retinal Vein Occlusion 53 0.532
329
P ESN008 Eosinophilic Pneumonia 50 0.532
330
HRP004 Herpes Zoster 60 0.532
331
KR001 Koro 19 0.532
332
P PRC019 Precocious Puberty 48 0.532
333
RYN005 Raynaud Phenomenon 45 0.532
334
P MCR129 Microvascular Complications of Diabetes 1 67 0.519
335
DBT002 Diabetic Autonomic Neuropathy 40 0.519
336
PRP027 Peripheral Vascular Disease 71 0.512
337
P LNG032 Lung Cancer 98 0.512
338
PHB003 Phobia, Specific 44 0.512
339
CNV002 Conversion Disorder 47 0.512
340
HGH043 High Grade Glioma 46 0.512
341
P DBT009 Diabetes Mellitus 67 0.512
342
CRH001 Crohn's Disease 80 0.512
343
c CHR684 Chronic Kidney Disease 73 0.512
344
PPL052 Papillomatosis, Confluent and Reticulated 34 0.401
345
GBM001 Gaba Aminotransferase Deficiency 31 0.396
346
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.396
347
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.396
348
BRN032 Brain Glioma 45 0.396
349
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.396
350
P CLD003 Cold-Induced Sweating Syndrome 42 0.396
351
c LNG044 Long Qt Syndrome 1 66 0.396
352
c TYP009 Type 2 Diabetes Mellitus 91 0.396
353
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.396
354
P HMN038 Human Coronavirus Sensitivity 30 0.396
355
P NJM001 Nijmegen Breakage Syndrome 75 0.396
356
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 35 0.396
357
c BRN108 Branchiootic Syndrome 1 63 0.396
358
ACR041 Acromelic Frontonasal Dysostosis 53 0.396
359
DNT045 Dental Anomalies and Short Stature 50 0.396
360
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.396
361
P GST053 Gastric Cancer 82 0.396
362
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.396
363
P PNC035 Pancreatic Cancer 87 0.396
364
ANG049 Angioedema Induced by Ace Inhibitors 38 0.396
365
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.396
366
ENH001 Enhanced S-Cone Syndrome 58 0.396
367
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.396
368
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 52 0.396
369
PLY105 Polycystic Ovary Syndrome 1 39 0.396
370
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 0.396
371
c DRR009 Diarrhea 6 46 0.396
372
LPT014 Leptin Deficiency or Dysfunction 77 0.396
373
LPT006 Leptin Receptor Deficiency 50 0.396
374
CHL065 Cholangiocarcinoma 57 0.396
375
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.396
376
c HYP595 Hypertension, Essential 84 0.396
377
P CNR004 Cone-Rod Dystrophy 2 74 0.396
378
ESP021 Esophageal Cancer 84 0.396
379
P GLM040 Glioma Susceptibility 1 70 0.396
380
AYM001 Ayme-Gripp Syndrome 57 0.396
381
c CTR110 Cataract 26, Multiple Types 26 0.396
382
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.396
383
VTM033 Vitamin K Deficiency Bleeding 49 0.396
384
HYP458 Hyper Ige Syndrome 60 0.396
385
CHL159 Childhood-Onset Asthma 30 0.396
386
DSS010 Dissociative Disorder 39 0.396
387
P MLN007 Male Infertility 56 0.396
388
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.396
389
P BLD062 Bile Duct Cancer 69 0.396
390
INT002 Intermittent Claudication 61 0.396
391
MXD026 Mixed Glioma 45 0.396
392
P GLL018 Gallbladder Cancer 59 0.396
393
P MTR014 Motor Neuron Disease 65 0.396
394
P PLY011 Polycystic Ovary Syndrome 57 0.396
395
RDN001 Reading Disorder 40 0.396
396
P PLY019 Polyneuropathy 52 0.396
397
c HMG001 Hemoglobin C Disease 41 0.396
398
INT079 Intrahepatic Cholangiocarcinoma 51 0.396
399
PRD004 Prediabetes Syndrome 52 0.396
400
VSL002 Visual Epilepsy 39 0.396
401
GLC003 Glucose Intolerance 53 0.396
402
KRT002 Keratomalacia 54 0.396
403
LWC001 Low Compliance Bladder 44 0.396
404
CNN001 Cannabis Dependence 37 0.396
405
P INF032 Infertility 60 0.396
406
PHB001 Phobic Disorder 45 0.396
407
LNG031 Lung Benign Neoplasm 51 0.396
408
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 0.396
409
CNN002 Cannabis Abuse 44 0.396
410
END086 End Stage Renal Disease 54 0.396
411
CYT018 Cytochrome P450 2d6 Variant 26 0.396
412
ATX019 Ataxia with Vitamin E Deficiency 44 0.396
414
P AMY004 Amyloidosis 69 0.396
415
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.396
416
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.396
417
P HYP086 Hypothyroidism 68 0.328
418
HYP066 Hyperglycemia 60 0.306
419
P BCL017 B-Cell Lymphoma 57 0.306
420
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.284
421
ATH013 Atherosclerosis Susceptibility 63 0.259
422
DMN031 Dementia, Lewy Body 65 0.259
423
P BLP003 Blepharospasm 45 0.259
424
SVR001 Severe Acute Respiratory Syndrome 68 0.259
425
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.232
426
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.232
427
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.232
428
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.232
429
LPD008 Lipid Metabolism Disorder 61 0.232
430
MTS001 Mutism 44 0.232
431
P GST044 Gastritis 55 0.232
432
ALX002 Alexithymia 36 0.201
433
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.201
434
P PTS002 Ptosis 52 0.201
435
P SLP006 Sleep Apnea 69 0.201
436
ERY003 Erythema Multiforme 56 0.201
437
GLL008 Gilles De La Tourette Syndrome 64 0.201
438
P TRT019 Torticollis 47 0.201
439
HYP020 Hyperprolactinemia 63 0.201
440
SVR097 Severe Cutaneous Adverse Reaction 68 0.201
441
c WLF013 Wolfram Syndrome 1 60 0.201
442
P HYD006 Hydrocephalus 62 0.201
443
CVD001 Covid-19 59 0.201
444
RGH001 Right Bundle Branch Block 47 0.201
445
ACT058 Active Peptic Ulcer Disease 55 0.201
446
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.201
447
DRG003 Drug Dependence 46 0.201
448
ERY066 Erythema Multiforme Major 29 0.201
449
c RNG015 Ring Chromosome 2 22 0.201
450
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.201
451
c MJR014 Major Depressive Disorder 2 13 0.164
452
P LYM118 Lymphoma 66 0.164
453
c DWL002 Dowling-Degos Disease 1 58 0.164
454
P RTT002 Rett Syndrome 79 0.164
455
P BLD134 Bladder Cancer 79 0.164
456
INS024 Insulin-Like Growth Factor I 77 0.164
457
FML037 Female Breast Cancer 51 0.164
458
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.164
459
ANN002 Anencephaly 57 0.164
460
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.164
461
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.164
462
BRK010 Burkitt Lymphoma 65 0.164
463
c HYP836 Hypercholesterolemia, Familial, 1 73 0.164
464
HRW001 Hair Whorl 35 0.164
465
P VNT002 Ventricular Septal Defect 58 0.164
466
FCL014 Focal Epilepsy 53 0.164
467
FCT008 Factitious Disorder 34 0.164
468
CNT047 Contact Dermatitis 56 0.164
469
CHL068 Cholestasis 61 0.164
470
ADJ001 Adjustment Disorder 46 0.164
471
DYS101 Dysgerminoma 43 0.164
472
P PRP019 Peripheral Nervous System Disease 57 0.164
473
BRN009 Burning Mouth Syndrome 51 0.164
474
CMP010 Complex Regional Pain Syndrome 59 0.164
475
P KDN017 Kidney Cancer 60 0.164
476
ALL010 Allergic Contact Dermatitis 55 0.164
477
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.164
478
PRT037 Pertussis 49 0.164
479
BRN028 Brain Cancer 73 0.164
480
P CTR002 Cataract 59 0.164
481
P VSC011 Vasculitis 61 0.164
482
P BRT004 Bartter Disease 58 0.164
483
RMS001 Rem Sleep Behavior Disorder 47 0.164
484
P NRP001 Neuropathy 59 0.164
485
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.164
486
MRC001 Marchiafava Bignami Disease 28 0.164
487
HYP855 Hyperpigmentation of the Skin 25 0.164
488
c ACT134 Acute Liver Failure 57 0.164
489
P OMP004 Omphalocele 47 0.116
490
PHN011 Phenytoin Toxicity 32 0.116
491
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.116
492
CRV043 Cervical Dystonia 46 0.116
493
c PRG020 Paragangliomas 3 39 0.116
494
VRC005 Varicose Veins 59 0.116
495
P NNN008 Noonan Syndrome 1 76 0.116
496
P OVR042 Ovarian Cancer 88 0.116
497
DSC013 Discrimination, Two-Point, Reduction in 21 0.116
498
P SRC025 Sarcoidosis 1 70 0.116
499
NRL016 Neural Tube Defects 80 0.116
500
P PRD006 Prader-Willi Syndrome 60 0.116
501
c GLC092 Glaucoma, Primary Open Angle 60 0.116
502
GST009 Gastroschisis 53 0.116
503
c OTP006 Otopalatodigital Syndrome, Type I 59 0.116
504
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.116
506
c RTN047 Retinitis Pigmentosa 18 45 0.116
507
VTM002 Vitamin B12 Deficiency 48 0.116
508
c LNG047 Long Qt Syndrome 2 59 0.116
509
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.116
510
FTL006 Fetal Alcohol Spectrum Disorder 43 0.116
511
DND001 Dandy-Walker Syndrome 48 0.116
512
ENT011 Enterocolitis 55 0.116
513
c TBR025 Tuberous Sclerosis 1 84 0.116
514
HMF011 Hemifacial Spasm, Familial 33 0.116
515
SDD001 Sudden Infant Death Syndrome 60 0.116
516
c GRV008 Graves Disease 1 54 0.116
517
c THR092 Thrombophilia Due to Thrombin Defect 74 0.116
518
OCL052 Ocular Dominance 40 0.116
519
CLF027 Cleft Palate, Isolated 64 0.116
520
MTN003 Motion Sickness 50 0.116
521
CD4008 Cd4/cd8 T-Cell Ratio 19 0.116
522
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.116
523
CHR346 Chromosome 22q11.2 Deletion Syndrome, Distal 36 0.116
524
P FTL001 Fetal Alcohol Syndrome 55 0.116
525
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 64 0.116
526
TRY001 Trypanosomiasis 50 0.116
527
RBS001 Rabies 57 0.116
528
ESP002 Esophageal Varix 51 0.116
529
MXD044 Mixed Sleep Apnea 21 0.116
530
P ALP004 Alport Syndrome 69 0.116
531
P CYS018 Cystitis 58 0.116
532
HYP030 Hypoactive Sexual Desire Disorder 40 0.116
533
P GRN010 Granular Cell Tumor 40 0.116
534
HYP080 Hypogonadism 49 0.116
535
c TRN005 Transient Tic Disorder 17 0.116
536
P ATR010 Atrial Heart Septal Defect 58 0.116
537
HYP014 Hyperuricemia 51 0.116
538
P TBR001 Tuberous Sclerosis 69 0.116
539
P SPN046 Spinal Muscular Atrophy 62 0.116
540
HRT011 Heart Septal Defect 49 0.116
541
P HYP730 Hypogonadotropic Hypogonadism 57 0.116
542
XLN231 X-Linked Alport Syndrome 41 0.116
543
MCL057 Macular Dystrophy with Central Cone Involvement 28 0.116
544
P ECL001 Eclampsia 52 0.116
545
CLL003 Cellulitis 53 0.116
546
ANT019 Anterograde Amnesia 38 0.116
547
FLL008 Folliculitis 45 0.116
548
c CNT035 Central Nervous System Disease 53 0.116
549
NCR004 Nocardiosis 52 0.116
550
P INT143 Interstitial Cystitis 59 0.116
551
P URN019 Urinary Tract Infection 48 0.116
552
GST037 Gastroparesis 52 0.116
553
P PRP029 Porphyria 60 0.116
554
PLM031 Poliomyelitis 62 0.116
555
THY030 Thyroid Gland Disease 50 0.116
556
P NRM002 Normal Pressure Hydrocephalus 49 0.116
557
KLV001 Kluver-Bucy Syndrome 34 0.116
558
P PNC044 Pancreatitis 61 0.116
559
c ACT027 Acute Pancreatitis 60 0.116
560
TST014 Testicular Cancer 51 0.116
561
P HYP061 Hypertrophic Cardiomyopathy 68 0.116
562
GTR002 Goiter 52 0.116
563
ATN004 Autonomic Neuropathy 42 0.116
564
CLB002 Clubfoot 50 0.116
565
c CHR056 Chronic Tic Disorder 36 0.116
566
P OPN001 Open-Angle Glaucoma 55 0.116
567
PRT013 Portal Hypertension 59 0.116
568
AMN003 Amnestic Disorder 53 0.116
569
KLP001 Kleptomania 36 0.116
570
c ACT068 Acute Cystitis 60 0.116
571
NSP002 Nasopharyngitis 45 0.116
572
c PRC016 Pre-Eclampsia 64 0.116
573
NRG002 Neurogenic Bladder 54 0.116
574
SLP001 Sleeping Sickness 56 0.116
575
CHR074 Choriocarcinoma 46 0.116
576
BRN024 Bronchitis 67 0.116
577
PLC008 Placenta Disease 48 0.116
578
ILS001 Ileus 49 0.116
579
P CMP008 Compartment Syndrome 49 0.116
580
ART012 Aortitis 41 0.116
581
ATH004 Athetosis 25 0.116
582
P ATR005 Atrophic Gastritis 50 0.116
583
SPC005 Speech Disorder 46 0.116
584
c ACT075 Acute Myocardial Infarction 55 0.116
585
PPT005 Peptic Ulcer Disease 58 0.116
586
P MSC003 Muscular Atrophy 52 0.116
587
CHL045 Choline Deficiency Disease 39 0.116
588
CRN088 Craniorachischisis 35 0.116
589
INT007 Intermediate Coronary Syndrome 53 0.116
590
ATP014 Atp8b1 Deficiency 28 0.116
591
DLS001 Delusional Disorder 44 0.116
592
GRN017 Granulocytopenia 42 0.116
593
RHH001 Rohhad 27 0.116
594
BCK006 Back Pain 43 0.116
595
P MNN013 Meningitis 65 0.116
596
PRM039 Primary Angiitis of the Central Nervous System 32 0.116
597
THN005 Thunderclap Headache 16 0.116
598
OVR094 Ovarian Epithelial Cancer 39 0.116
599
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.116
600
ELC001 Elective Mutism 22 0.116
601
HYP056 Hypoglycemia 65 0.116
603
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.116
604
MTR086 Motor Stereotypies 14 0.116
605
PRG033 Progressive Non-Fluent Aphasia 52 0.116
606
c PSD047 Pseudo-Turner Syndrome 52 0.116
607
ABD010 Abdominal Wall Defect 37 0.116
608
PST103 Postpartum Psychosis 31 0.116
609
MTR087 Maternal Uniparental Disomy 28 0.116
610
MST020 Mast Cell Activation Syndrome 27 0.116
611
ADG002 Audiogenic Seizures 25 0.116
612
SMN008 Semantic Dementia 46 0.116
613
P HMF004 Hemifacial Spasm 38 0.116
614
SPC030 Specific Language Disorder 25 0.116
615
CRD137 Cardiogenic Shock 56 0.116
Content
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