Search results for Citalopram

448 hits were found for Citalopram

# Family MCID Name MIFTS Score
1
P MJR001 Major Depressive Disorder 68 4.930
2
DPR016 Depression 63 0.556
3
MNT002 Mental Depression 58 0.530
4
END040 Endogenous Depression 55 0.322
5
NRT001 Neurotic Disorder 53 0.308
6
ANX010 Anxiety 73 0.284
7
OBS002 Obsessive-Compulsive Disorder 68 0.220
8
SRT004 Serotonin Syndrome 47 0.185
9
P PNC025 Panic Disorder 53 0.168
10
P DMN002 Dementia 66 0.165
11
PSY004 Psychotic Disorder 67 0.159
12
P ALZ034 Alzheimer Disease 88 0.152
13
ALC007 Alcohol Dependence 66 0.152
14
DSS008 Disease of Mental Health 58 0.149
15
P TRM003 Tremor 54 0.149
16
P PRS038 Personality Disorder 65 0.135
17
SXL003 Sexual Disorder 47 0.135
18
P SCH015 Schizophrenia 74 0.131
19
c ATS007 Autism Spectrum Disorder 67 0.123
20
KHL003 Kohlschutter-Tonz Syndrome 65 0.123
21
P BPL003 Bipolar Disorder 56 0.123
22
c MJR024 Major Affective Disorder 9 41 0.123
23
c MJR022 Major Affective Disorder 8 38 0.123
24
P ATS364 Autism 70 0.119
25
MDD011 Mood Disorder 62 0.119
26
VSL002 Visual Epilepsy 59 0.119
27
SCL003 Social Phobia 48 0.119
28
LPP008 Lipoprotein Quantitative Trait Locus 62 0.114
29
P PRV006 Pervasive Developmental Disorder 57 0.114
30
P SZR006 Seizure Disorder 56 0.114
31
SVR004 Severe Combined Immunodeficiency 73 0.105
32
P ALC033 Alcohol Use Disorder 58 0.105
33
GNR004 Generalized Anxiety Disorder 56 0.105
34
DYS009 Dysthymic Disorder 49 0.100
35
P MJR007 Major Affective Disorder 1 43 0.100
36
c MJR008 Major Affective Disorder 2 35 0.100
37
c MJR023 Major Affective Disorder 7 33 0.100
38
c MJR003 Major Affective Disorder 6 33 0.100
39
c MJR006 Major Affective Disorder 5 33 0.100
40
c MJR004 Major Affective Disorder 4 28 0.100
41
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.095
42
ADL002 Adult Syndrome 70 0.095
43
IRR002 Irritable Bowel Syndrome 65 0.095
44
ETN001 Eating Disorder 60 0.095
45
BRN071 Brain Injury 49 0.095
46
CYT018 Cytochrome P450 2d6 Variant 27 0.095
47
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.090
48
GST092 Gastroesophageal Reflux 67 0.090
49
P TRN020 Turner Syndrome 67 0.090
50
c RHB024 Rhabdomyosarcoma 2 67 0.090
51
P LNG028 Long Qt Syndrome 66 0.090
52
ALL026 Allergic Hypersensitivity Disease 62 0.090
53
SCH003 Schizophreniform Disorder 56 0.090
54
TRM010 Traumatic Brain Injury 51 0.090
55
INP001 Inappropriate Adh Syndrome 49 0.090
56
CCN002 Cocaine Abuse 49 0.090
57
P CHR345 Chronic Pain 44 0.090
58
PRM003 Premature Ejaculation 44 0.090
59
MLN003 Melancholia 38 0.090
60
STR067 Stroke, Ischemic 81 0.084
61
c MGR028 Migraine with or Without Aura 1 67 0.084
62
c HPT001 Hepatitis C 62 0.084
63
CRD132 Cardiac Conduction Defect 58 0.084
64
AVD001 Avoidant Personality Disorder 51 0.084
65
CCN001 Cocaine Dependence 48 0.084
66
P HPT021 Hepatitis 67 0.078
67
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.078
68
LVR012 Liver Cirrhosis 62 0.078
69
PST028 Post-Traumatic Stress Disorder 58 0.078
70
ISC004 Ischemia 58 0.078
71
CNS004 Constipation 58 0.078
72
ART140 Arteries, Anomalies of 52 0.078
73
SMT001 Somatization Disorder 46 0.078
74
AGR002 Agoraphobia 45 0.078
75
CYT002 Cytokine Deficiency 42 0.078
76
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.078
77
P KDN018 Kidney Disease 72 0.071
78
P FRN006 Frontotemporal Dementia 68 0.071
79
CRB039 Cerebrovascular Disease 67 0.071
80
P ENC018 Encephalopathy 61 0.071
81
P EXN002 Exanthem 57 0.071
82
BRD004 Borderline Personality Disorder 53 0.071
83
OCL069 Ocular Motor Apraxia 51 0.071
84
P ASP001 Asperger Syndrome 48 0.071
85
ACT084 Acute Stress Disorder 47 0.071
86
ATN005 Autonomic Dysfunction 46 0.071
87
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.071
88
SBC016 Subacute Delirium 44 0.071
89
48X005 48,xyyy 39 0.071
90
CHL079 Children's Interstitial Lung Disease 26 0.071
91
P BRS047 Breast Cancer 97 0.064
92
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.064
93
IMM167 Immune Deficiency Disease 78 0.064
94
P PRK057 Parkinson Disease, Late-Onset 78 0.064
95
P HNT016 Huntington Disease 72 0.064
96
P EPL164 Epilepsy 71 0.064
97
P HYP086 Hypothyroidism 69 0.064
98
P LVR013 Liver Disease 68 0.064
99
P CRD119 Cardiac Arrest 67 0.064
100
ANG054 Angina Pectoris 66 0.064
101
ACR006 Aceruloplasminemia 65 0.064
102
P FRD001 Friedreich Ataxia 64 0.064
103
P CRN300 Coronary Heart Disease 1 63 0.064
104
ANR007 Anorexia Nervosa 63 0.064
105
c PNS012 Paine Syndrome 61 0.064
106
HPT019 Hepatic Encephalopathy 60 0.064
107
FBR047 Fibromyalgia 58 0.064
108
P HDC001 Headache 57 0.064
109
APH002 Aphasia 57 0.064
110
VSC002 Vascular Dementia 57 0.064
111
NRL004 Neuroleptic Malignant Syndrome 56 0.064
112
P SBS003 Substance Abuse 55 0.064
113
IMP005 Impotence 52 0.064
114
PST021 Postpartum Depression 50 0.064
115
SMT006 Somatoform Disorder 50 0.064
116
OBS003 Obsessive-Compulsive Personality Disorder 46 0.064
117
OPD001 Opioid Abuse 46 0.064
118
SYN036 Syncope 45 0.064
119
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.064
120
HPT004 Hepatic Coma 45 0.064
121
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.064
122
PRM020 Premenstrual Tension 40 0.064
123
c CHR682 Chronic Bilirubin Encephalopathy 39 0.064
124
PSD088 Pseudobulbar Affect 36 0.064
125
P HRT032 Heart Disease 75 0.055
126
HMN044 Human Immunodeficiency Virus Type 1 71 0.055
127
P MYC007 Myocardial Infarction 70 0.055
128
P OCL013 Oculodentodigital Dysplasia 69 0.055
129
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.055
130
c MCR129 Microvascular Complications of Diabetes 1 66 0.055
131
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.055
132
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.055
133
P GLM045 Glioma 63 0.055
134
P VSC007 Vascular Disease 63 0.055
135
P MVM001 Movement Disease 63 0.055
136
c FNC043 Fanconi Anemia, Complementation Group E 62 0.055
137
NTR005 Nutritional Deficiency Disease 62 0.055
138
CHR066 Chronic Fatigue Syndrome 61 0.055
139
CRD223 Cardiac Arrhythmia 60 0.055
140
P SLP005 Sleep Disorder 59 0.055
141
PRT058 Pure Autonomic Failure 59 0.055
142
BLM002 Bulimia Nervosa 57 0.055
143
CHR105 Choreoacanthocytosis 57 0.055
144
P CRD246 Cardiovascular System Disease 57 0.055
145
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.055
146
AGN016 Aging 56 0.055
147
HYP005 Hypokalemia 55 0.055
148
AMN001 Amenorrhea 54 0.055
149
DBT010 Diabetic Neuropathy 54 0.055
150
P TCD001 Tic Disorder 53 0.055
151
P SHR001 Short Bowel Syndrome 53 0.055
152
PNG002 Pain Agnosia 51 0.055
153
SCH012 Schizoaffective Disorder 50 0.055
154
P TMP001 Temporal Lobe Epilepsy 50 0.055
155
OPT003 Opiate Dependence 50 0.055
156
47X002 47,xyy 49 0.055
157
BKR002 Baker-Gordon Syndrome 49 0.055
158
URM002 Uremia 49 0.055
159
PRP007 Priapism 47 0.055
160
P MYC033 Myoclonus 46 0.055
161
GLL048 Glial Tumor 45 0.055
162
CRB004 Cerebral Artery Occlusion 45 0.055
163
SPS057 Spasticity 45 0.055
164
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.055
165
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.055
166
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.055
167
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.055
168
ATX019 Ataxia with Vitamin E Deficiency 42 0.055
169
49X006 49, Xxxxy Syndrome 41 0.055
170
P HYP263 Hypersomnia 41 0.055
171
PRR013 Prurigo Nodularis 36 0.055
172
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.055
173
HND015 Hand Skill, Relative 33 0.055
174
CGN007 Cognitive Function 1, Social 27 0.055
175
BNG077 Benign Idiopathic Neonatal Seizures 26 0.055
176
P CLR023 Colorectal Cancer 99 0.045
177
c LKM061 Leukemia, Acute Myeloid 84 0.045
178
P RHM011 Rheumatoid Arthritis 80 0.045
179
AST005 Asthma 76 0.045
180
P RSP003 Respiratory Failure 74 0.045
181
P OST002 Osteoporosis 74 0.045
182
P MLT020 Multiple Sclerosis 72 0.045
183
DWN001 Down Syndrome 70 0.045
184
P ART022 Arthritis 69 0.045
185
P SLP006 Sleep Apnea 69 0.045
186
P CRN037 Craniosynostosis 68 0.045
187
PCK003 Pick Disease of Brain 68 0.045
188
P THR014 Thrombocytopenia 67 0.045
189
P PLM037 Pulmonary Hypertension 67 0.045
190
P DYS154 Dystonia 65 0.045
191
BRR014 Barrett Esophagus 65 0.045
192
ATH013 Atherosclerosis Susceptibility 65 0.045
193
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.045
194
TRN015 Transient Cerebral Ischemia 63 0.045
195
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.045
196
c HPT003 Hepatitis a 62 0.045
197
P MCH002 Machado-Joseph Disease 62 0.045
198
P ESP024 Esophagitis 62 0.045
199
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.045
200
ATM095 Autoimmune Disease 62 0.045
201
OST003 Osteonecrosis 61 0.045
202
P LPS004 Lupus Erythematosus 61 0.045
203
ACQ007 Acquired Immunodeficiency Syndrome 60 0.045
204
STT001 Status Epilepticus 60 0.045
205
c ACT071 Acute Kidney Failure 60 0.045
206
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.045
207
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.045
208
P ESP035 Esophagitis, Eosinophilic, 1 57 0.045
209
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.045
210
P DRR001 Diarrhea 55 0.045
211
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.045
213
ESN005 Eosinophilic Gastroenteritis 55 0.045
214
TRD006 Tardive Dyskinesia 54 0.045
215
P ALP008 Alopecia 54 0.045
216
GST023 Gastric Ulcer 53 0.045
217
PRP080 Peripheral Artery Disease 53 0.045
218
CHR073 Choreatic Disease 52 0.045
219
P NRC002 Narcolepsy 52 0.045
220
PTH003 Pathologic Nystagmus 52 0.045
221
PPT001 Peptic Esophagitis 52 0.045
222
TRC010 Trichotillomania 51 0.045
223
PTH002 Pathological Gambling 49 0.045
224
WTH001 Withdrawal Disorder 48 0.045
225
SBS004 Substance Dependence 48 0.045
226
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.045
227
OPD006 Opioid Addiction 48 0.045
228
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.045
229
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.045
230
ATY001 Atypical Depressive Disorder 45 0.045
231
IMP006 Impulse Control Disorder 45 0.045
232
DPR002 Depersonalization Disorder 43 0.045
233
PHY002 Physical Disorder 42 0.045
234
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.045
235
GLC096 Galactorrhea 42 0.045
236
MYF002 Myofascial Pain Syndrome 42 0.045
237
DYS011 Dyskinesia of Esophagus 41 0.045
238
DBT002 Diabetic Autonomic Neuropathy 41 0.045
239
BDY001 Body Dysmorphic Disorder 40 0.045
240
HYP264 Hypertonia 38 0.045
241
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.045
242
WHP002 Whiplash 36 0.045
243
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.045
244
DPN001 Dependent Personality Disorder 30 0.045
245
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.045
247
FBR090 Fibro-Adipose Vascular Anomaly 17 0.045
248
c BNM021 Bone Mineral Density Quantitative Trait Locus 7 13 0.045
249
P HPT023 Hepatocellular Carcinoma 100 0.032
250
P LNG032 Lung Cancer 98 0.032
251
ESP021 Esophageal Cancer 90 0.032
252
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.032
253
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.032
254
c SYS001 Systemic Lupus Erythematosus 86 0.032
255
c HYP595 Hypertension, Essential 84 0.032
256
P PNC035 Pancreatic Cancer 84 0.032
257
P GST053 Gastric Cancer 83 0.032
258
P GLM040 Glioma Susceptibility 1 81 0.032
259
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.032
260
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.032
261
GLB015 Glioblastoma Multiforme 75 0.032
262
LPT014 Leptin Deficiency or Dysfunction 74 0.032
263
c HYP836 Hypercholesterolemia, Familial, 1 73 0.032
264
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.032
265
c HPT073 Hepatitis C Virus 72 0.032
266
P NRB001 Neuroblastoma 72 0.032
267
PRP027 Peripheral Vascular Disease 71 0.032
268
DFC004 Deficiency Anemia 70 0.032
269
P AMY004 Amyloidosis 70 0.032
270
c CHR684 Chronic Kidney Disease 70 0.032
271
P MYP004 Myopathy 70 0.032
272
CNG034 Congestive Heart Failure 69 0.032
273
P MLN008 Melanoma 69 0.032
274
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.032
275
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.032
276
CHL065 Cholangiocarcinoma 68 0.032
277
SKN019 Skin Melanoma 68 0.032
278
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.032
279
P BLD062 Bile Duct Cancer 67 0.032
280
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.032
281
P SKN015 Skin Carcinoma 66 0.032
282
HYP056 Hypoglycemia 66 0.032
283
c LNG044 Long Qt Syndrome 1 66 0.032
284
P HYD006 Hydrocephalus 66 0.032
285
c SML038 Small Cell Cancer of the Lung 65 0.032
286
P MTR014 Motor Neuron Disease 65 0.032
287
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.032
288
P ADL010 Adult Respiratory Distress Syndrome 65 0.032
289
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.032
290
P DBT009 Diabetes Mellitus 64 0.032
291
TBC004 Tobacco Addiction 64 0.032
292
BRC012 Brucellosis 64 0.032
293
OST017 Osteomyelitis 64 0.032
294
c BRN108 Branchiootic Syndrome 1 62 0.032
295
P HYP750 Hypertriglyceridemia, Familial 62 0.032
296
INT002 Intermittent Claudication 61 0.032
297
P MYL006 Myeloid Leukemia 60 0.032
298
SPN186 Spinal Cord Injury 60 0.032
299
HRP004 Herpes Zoster 60 0.032
300
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.032
301
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.032
302
P ALP009 Alopecia Areata 60 0.032
303
P SNS001 Sensorineural Hearing Loss 60 0.032
304
SPP011 Suppression of Tumorigenicity 12 59 0.032
305
P MCR010 Microcephaly 59 0.032
306
c HPT016 Hepatitis B 59 0.032
307
WLF002 Wolf-Hirschhorn Syndrome 59 0.032
308
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.032
309
TTZ003 Tietz Albinism-Deafness Syndrome 58 0.032
310
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.032
311
P GLL018 Gallbladder Cancer 57 0.032
312
P INF032 Infertility 57 0.032
313
P RHN004 Rhinitis 57 0.032
314
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.032
315
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.032
316
PHR003 Pharyngitis 57 0.032
317
AYM001 Ayme-Gripp Syndrome 57 0.032
318
P PLY011 Polycystic Ovary Syndrome 56 0.032
319
c ESS001 Essential Tremor 56 0.032
320
P NRP001 Neuropathy 56 0.032
321
PRS047 Prostatitis 56 0.032
322
GST050 Gastrointestinal System Disease 56 0.032
323
P PLY019 Polyneuropathy 56 0.032
324
ATR057 Atrioventricular Block 55 0.032
325
MCL006 Macular Retinal Edema 55 0.032
326
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.032
327
P MLN007 Male Infertility 55 0.032
328
P MYP006 Myopia 55 0.032
329
HMP005 Hemiplegia 55 0.032
330
INT007 Intermediate Coronary Syndrome 55 0.032
331
P NRM002 Normal Pressure Hydrocephalus 54 0.032
332
GLC003 Glucose Intolerance 54 0.032
333
P RST001 Restless Legs Syndrome 54 0.032
334
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.032
335
P LTR001 Lateral Sclerosis 54 0.032
336
NNL006 Non-Alcoholic Steatohepatitis 54 0.032
337
PRS045 Prostatic Hypertrophy 53 0.032
338
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.032
339
c CNT016 Central Retinal Vein Occlusion 53 0.032
340
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.032
341
P CTN003 Cutaneous Lupus Erythematosus 53 0.032
342
P RTN022 Retinal Vein Occlusion 53 0.032
343
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.032
344
c FML191 Familial Long Qt Syndrome 53 0.032
345
P ATN002 Autonomic Nervous System Disease 52 0.032
346
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.032
347
STT041 Stuttering 52 0.032
348
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.032
349
ACR041 Acromelic Frontonasal Dysostosis 52 0.032
350
NRT004 Neuritis 52 0.032
351
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.032
352
P RCT021 Rectum Cancer 52 0.032
353
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.032
354
P MGR003 Migraine with Aura 52 0.032
355
P OLV001 Olivopontocerebellar Atrophy 51 0.032
356
PRS021 Prostatic Adenoma 51 0.032
357
P LCT001 Lactic Acidosis 51 0.032
358
INT079 Intrahepatic Cholangiocarcinoma 51 0.032
359
LNG031 Lung Benign Neoplasm 51 0.032
360
END086 End Stage Renal Disease 51 0.032
361
BRX001 Bruxism 50 0.032
362
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.032
363
P ESN008 Eosinophilic Pneumonia 50 0.032
364
MTB004 Metabolic Acidosis 50 0.032
365
DYS073 Dysphagia 50 0.032
366
AMB002 Amblyopia 49 0.032
367
GYN001 Gynecomastia 49 0.032
368
LFT001 Left Bundle Branch Hemiblock 49 0.032
369
PRS129 Prostatic Hyperplasia, Benign 49 0.032
370
c BPL002 Bipolar I Disorder 49 0.032
371
P MGR001 Migraine Without Aura 49 0.032
372
DNT045 Dental Anomalies and Short Stature 49 0.032
373
VTM033 Vitamin K Deficiency Bleeding 48 0.032
374
INT067 Interstitial Nephritis 48 0.032
375
LPT006 Leptin Receptor Deficiency 48 0.032
376
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.032
377
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.032
378
DRG003 Drug Dependence 47 0.032
379
PRD004 Prediabetes Syndrome 47 0.032
380
HYP016 Hypochondriasis 47 0.032
381
ANT011 Antisocial Personality Disorder 47 0.032
382
c CNG216 Congenital Hydrocephalus 47 0.032
383
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.032
384
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.032
385
RYN005 Raynaud Phenomenon 47 0.032
386
P PRC019 Precocious Puberty 46 0.032
387
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.032
388
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.032
389
c SCH079 Schizophrenia 1 46 0.032
390
CRN019 Coronary Artery Vasospasm 46 0.032
391
c DRR009 Diarrhea 6 46 0.032
392
c MLG068 Malignant Glioma 46 0.032
393
MXD026 Mixed Glioma 45 0.032
394
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.032
395
CNV002 Conversion Disorder 45 0.032
396
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.032
397
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.032
398
BRN032 Brain Glioma 45 0.032
399
CRT015 Carotid Artery Occlusion 45 0.032
400
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.032
401
CNN002 Cannabis Abuse 44 0.032
402
c HYP272 Hypercholesterolemia, Familial, 3 44 0.032
403
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.032
404
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.032
405
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.032
406
LWC001 Low Compliance Bladder 43 0.032
407
PLY068 Polysubstance Abuse 43 0.032
408
P HYP265 Hypotonia 43 0.032
409
HYP457 Hypertrophic Scars 42 0.032
411
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.032
412
PHB001 Phobic Disorder 41 0.032
413
GST020 Gastric Antral Vascular Ectasia 41 0.032
414
PRM013 Premature Menopause 41 0.032
415
INF159 Infantile Sialic Acid Storage Disease 41 0.032
416
INT025 Intermittent Explosive Disorder 41 0.032
417
PRS063 Paresthesia 41 0.032
418
PHB003 Phobia, Specific 41 0.032
419
NNT008 Neonatal Abstinence Syndrome 41 0.032
420
RDN001 Reading Disorder 40 0.032
421
c HMG001 Hemoglobin C Disease 40 0.032
422
ANG049 Angioedema Induced by Ace Inhibitors 40 0.032
423
CNN001 Cannabis Dependence 40 0.032
424
MLT001 Multiple Chemical Sensitivity 40 0.032
425
P DYS021 Dysautonomia 39 0.032
426
SPP007 Suppression Amblyopia 39 0.032
427
DSS010 Dissociative Disorder 39 0.032
428
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.032
429
ALX002 Alexithymia 38 0.032
430
ALL014 Allergic Encephalomyelitis 38 0.032
431
c PLY105 Polycystic Ovary Syndrome 1 38 0.032
432
SPR012 Separation Anxiety Disorder 38 0.032
433
c SYS043 Systemic Lupus Erythematosus 1 38 0.032
434
P CRB059 Cerebellar Degeneration 37 0.032
435
P CLD003 Cold-Induced Sweating Syndrome 37 0.032
436
OBS015 Obesity, Hyperphagia, and Developmental Delay 36 0.032
437
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.032
438
INF021 Infant Gynecomastia 31 0.032
439
P ACT028 Acute Closed-Angle Glaucoma 30 0.032
440
MLT116 Multiple System Atrophy, Parkinsonian Type 30 0.032
441
ANS006 Anosognosia 30 0.032
442
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.032
443
ANS021 Anisocoria 27 0.032
444
KR001 Koro 24 0.032
445
CHR247 Chromosome 4p Deletion 22 0.032
446
c PNC122 Panic Disorder 1 19 0.032
447
ATM054 Autoimmune Disease 3 18 0.032
448
c INF047 Infantile Free Sialic Acid Storage Disease 17 0.032
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