Search results for Fluoxetine

840 hits were found for Fluoxetine

# Family MCID Name MIFTS Score
1
MNT002 Mental Depression 56 22.639
2
DPR016 Depression 65 20.858
3
P MJR001 Major Depressive Disorder 68 19.640
4
OBS002 Obsessive-Compulsive Disorder 68 12.432
5
END040 Endogenous Depression 54 10.695
6
NRT001 Neurotic Disorder 56 9.056
7
ANX010 Anxiety 70 8.281
8
MDD011 Mood Disorder 62 7.849
9
P BPL003 Bipolar Disorder 56 7.439
10
c MJR024 Major Affective Disorder 9 40 7.364
11
c MJR022 Major Affective Disorder 8 37 7.364
12
STR067 Stroke, Ischemic 79 7.079
13
P PRS038 Personality Disorder 65 6.993
14
BLM002 Bulimia Nervosa 57 6.982
15
PST028 Post-Traumatic Stress Disorder 59 6.567
16
ETN001 Eating Disorder 59 6.265
17
P ATS364 Autism 72 6.109
18
PRM020 Premenstrual Tension 39 6.075
19
SXL003 Sexual Disorder 49 6.062
20
P PNC025 Panic Disorder 52 6.032
21
ALC007 Alcohol Dependence 65 5.725
22
P SZR006 Seizure Disorder 69 5.586
23
ANR007 Anorexia Nervosa 59 5.168
24
ACT084 Acute Stress Disorder 53 5.144
25
P MJR007 Major Affective Disorder 1 42 4.582
26
SRT004 Serotonin Syndrome 54 4.510
27
SCL003 Social Phobia 48 4.420
28
DYS009 Dysthymic Disorder 51 4.416
29
DWN001 Down Syndrome 70 4.170
30
P PLM037 Pulmonary Hypertension 69 4.158
31
P TRM003 Tremor 50 4.087
32
P ALC033 Alcohol Use Disorder 67 4.070
33
c PLM164 Pulmonary Hypertension, Primary, 1 80 4.035
34
FBR047 Fibromyalgia 58 4.023
35
CRB039 Cerebrovascular Disease 65 3.917
36
HYP056 Hypoglycemia 65 3.900
37
P EPL164 Epilepsy 70 3.863
38
PRM003 Premature Ejaculation 44 3.822
39
PSY004 Psychotic Disorder 66 3.771
40
c ATS007 Autism Spectrum Disorder 72 3.696
41
P ATT013 Attention Deficit-Hyperactivity Disorder 66 3.663
42
PRT058 Pure Autonomic Failure 58 3.643
43
GNR004 Generalized Anxiety Disorder 55 3.612
44
c BPL002 Bipolar I Disorder 47 3.550
45
BRD004 Borderline Personality Disorder 53 3.523
46
ISC004 Ischemia 61 3.491
47
AVD001 Avoidant Personality Disorder 49 3.478
48
CNS004 Constipation 56 3.433
49
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.412
50
P SBS003 Substance Abuse 54 3.335
51
PNG002 Pain Agnosia 51 3.307
52
CCN002 Cocaine Abuse 49 3.278
53
BDY001 Body Dysmorphic Disorder 40 3.136
54
TBC004 Tobacco Addiction 63 3.134
55
P MLT020 Multiple Sclerosis 79 3.104
56
AGN016 Aging 54 3.103
57
MLN003 Melancholia 41 3.060
58
OBS003 Obsessive-Compulsive Personality Disorder 43 3.058
59
CCN001 Cocaine Dependence 48 3.022
60
c MJR008 Major Affective Disorder 2 34 3.021
61
c MJR006 Major Affective Disorder 5 32 3.021
62
c MJR003 Major Affective Disorder 6 32 3.021
63
c MJR004 Major Affective Disorder 4 28 3.021
64
c MJR023 Major Affective Disorder 7 33 3.021
65
CNN001 Cannabis Dependence 38 2.996
66
P DBT009 Diabetes Mellitus 67 2.964
67
c TYP008 Type 1 Diabetes Mellitus 77 2.953
68
DPR002 Depersonalization Disorder 41 2.914
69
HYP266 Hypoxia 56 2.903
70
CNN002 Cannabis Abuse 44 2.847
71
ADL002 Adult Syndrome 69 2.819
72
P SLP005 Sleep Disorder 62 2.811
73
ATY001 Atypical Depressive Disorder 45 2.804
74
PST021 Postpartum Depression 50 2.800
75
ANT039 Antisynthetase Syndrome 55 2.769
76
P SLP006 Sleep Apnea 69 2.759
77
c PNS012 Paine Syndrome 60 2.754
78
SVR004 Severe Combined Immunodeficiency 71 2.676
79
MLD017 Mal De Debarquement Syndrome 33 2.665
80
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 2.653
81
SBC016 Subacute Delirium 42 2.635
82
TRC010 Trichotillomania 50 2.629
83
P DYS154 Dystonia 64 2.613
84
48X005 48,xyyy 39 2.592
85
SYN036 Syncope 44 2.571
86
HMN044 Human Immunodeficiency Virus Type 1 76 2.542
87
LPT014 Leptin Deficiency or Dysfunction 77 2.539
88
INT025 Intermittent Explosive Disorder 39 2.532
89
CYT002 Cytokine Deficiency 43 2.520
90
c MGR028 Migraine with or Without Aura 1 64 2.511
91
c TYP009 Type 2 Diabetes Mellitus 92 2.448
92
P MYC033 Myoclonus 46 2.442
93
c MYS046 Myasthenic Syndrome, Congenital, 1a, Slow-Channel 44 2.422
94
P LNG032 Lung Cancer 98 2.411
95
c SML038 Small Cell Cancer of the Lung 69 2.411
96
HMP005 Hemiplegia 53 2.411
97
MLT157 Multiple System Atrophy 1 69 2.383
98
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.334
99
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.334
100
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.334
101
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.334
102
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.334
103
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.334
104
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.334
105
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.334
106
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.334
107
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.334
108
P HNT016 Huntington Disease 73 2.312
109
IMP005 Impotence 52 2.306
110
LPT006 Leptin Receptor Deficiency 50 2.291
111
CRH001 Crohn's Disease 80 2.284
112
IMP006 Impulse Control Disorder 45 2.263
113
P DMN002 Dementia 65 2.249
114
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.241
115
EPT021 Epithelial Recurrent Erosion Dystrophy 46 2.241
116
PSD088 Pseudobulbar Affect 33 2.229
117
HYP016 Hypochondriasis 47 2.221
118
FCL014 Focal Epilepsy 53 2.204
119
BRN071 Brain Injury 50 2.191
120
RHB024 Rhabdomyosarcoma 2 65 2.179
121
P ANR048 Aniridia 1 66 2.179
122
P SCH015 Schizophrenia 74 2.169
123
P PRV006 Pervasive Developmental Disorder 52 2.150
124
P HDC001 Headache 56 2.141
125
P PRK039 Parkinsonism 55 2.139
126
GLM045 Glioma 62 2.103
127
GLL048 Glial Tumor 52 2.103
128
END086 End Stage Renal Disease 54 2.078
129
P EXN002 Exanthem 58 2.053
130
ADG002 Audiogenic Seizures 25 2.038
131
P ENC018 Encephalopathy 62 2.022
132
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.021
133
P CHR345 Chronic Pain 50 2.018
134
P NRB001 Neuroblastoma 66 2.018
135
DSS008 Disease of Mental Health 74 2.013
136
CNT015 Central Sleep Apnea 46 1.994
137
CHR066 Chronic Fatigue Syndrome 60 1.994
138
NTR005 Nutritional Deficiency Disease 60 1.983
139
P TCD001 Tic Disorder 50 1.975
140
CVD001 Covid-19 58 1.971
141
P CNG001 Congenital Myasthenic Syndrome 68 1.966
142
ACQ007 Acquired Immunodeficiency Syndrome 58 1.936
143
P NRV007 Nervous System Disease 66 1.918
144
P VSC007 Vascular Disease 62 1.902
145
SPN186 Spinal Cord Injury 61 1.897
146
SCH003 Schizophreniform Disorder 54 1.884
147
BCK006 Back Pain 43 1.882
148
AND005 Androgen Insensitivity Syndrome, Mild 21 1.867
149
MTS001 Mutism 44 1.865
150
TRM010 Traumatic Brain Injury 50 1.845
151
OCL052 Ocular Dominance 40 1.829
152
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.825
153
PHB001 Phobic Disorder 45 1.815
154
CRB004 Cerebral Artery Occlusion 46 1.812
155
P RSP003 Respiratory Failure 74 1.796
156
INP001 Inappropriate Adh Syndrome 48 1.780
157
SPR012 Separation Anxiety Disorder 41 1.754
158
ELC001 Elective Mutism 22 1.749
159
IRR002 Irritable Bowel Syndrome 65 1.730
160
CNT097 Central Hypoventilation Syndrome, Congenital 70 1.728
161
c HYP595 Hypertension, Essential 84 1.728
162
CYT018 Cytochrome P450 2d6 Variant 26 1.728
163
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.728
164
P TMP001 Temporal Lobe Epilepsy 49 1.717
165
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.716
166
OPT003 Opiate Dependence 49 1.716
167
DBT010 Diabetic Neuropathy 54 1.713
168
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.711
169
GST092 Gastroesophageal Reflux 60 1.707
170
STT001 Status Epilepticus 58 1.698
171
TRD006 Tardive Dyskinesia 53 1.693
172
P DRR001 Diarrhea 55 1.692
173
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.689
174
P TRN020 Turner Syndrome 67 1.665
175
MYF002 Myofascial Pain Syndrome 46 1.665
176
P ALZ034 Alzheimer Disease 87 1.646
177
P HYP263 Hypersomnia 40 1.646
178
WTH001 Withdrawal Disorder 47 1.635
179
P PRK057 Parkinson Disease, Late-Onset 79 1.617
180
P MVM001 Movement Disease 61 1.617
181
SBS004 Substance Dependence 46 1.612
182
VSC002 Vascular Dementia 59 1.601
183
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.595
184
P PRD006 Prader-Willi Syndrome 60 1.589
185
SMT006 Somatoform Disorder 50 1.582
186
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.579
187
CHR073 Choreatic Disease 53 1.579
188
AGR002 Agoraphobia 45 1.570
189
PST011 Pustulosis of Palm and Sole 52 1.557
190
P PSR002 Psoriasis 63 1.557
191
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 35 1.546
192
BRX001 Bruxism 51 1.536
193
OPD001 Opioid Abuse 44 1.535
194
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 1.526
195
HMR039 Hemorrhage, Intracerebral 57 1.526
196
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.526
197
VSL002 Visual Epilepsy 39 1.526
198
CRB009 Cerebritis 43 1.526
199
SMT001 Somatization Disorder 50 1.507
200
P HRT032 Heart Disease 84 1.493
201
RYN005 Raynaud Phenomenon 45 1.489
202
OCL069 Ocular Motor Apraxia 57 1.477
203
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.477
204
HYP020 Hyperprolactinemia 63 1.467
205
ALL029 Allergic Disease 61 1.467
206
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.461
207
SCH012 Schizoaffective Disorder 49 1.457
208
CMB002 Combat Disorder 30 1.450
209
AMB002 Amblyopia 49 1.436
210
SPP007 Suppression Amblyopia 38 1.436
211
PRP015 Paraphilia Disorder 32 1.425
212
P KDN018 Kidney Disease 72 1.422
213
P CRD119 Cardiac Arrest 68 1.418
214
CND002 Conduct Disorder 50 1.413
215
P URT039 Urticaria 57 1.413
216
PHY002 Physical Disorder 41 1.409
217
GLC003 Glucose Intolerance 53 1.380
218
DRM006 Dermatitis 62 1.378
219
P INF032 Infertility 60 1.357
220
47X002 47,xyy 48 1.352
221
P CRD246 Cardiovascular System Disease 55 1.346
222
LNG031 Lung Benign Neoplasm 51 1.346
223
LNG039 Lung Squamous Cell Carcinoma 57 1.346
224
c CNT035 Central Nervous System Disease 53 1.346
225
P LNG035 Lung Large Cell Carcinoma 53 1.346
226
STT041 Stuttering 52 1.341
227
LPD008 Lipid Metabolism Disorder 61 1.340
228
SVR001 Severe Acute Respiratory Syndrome 68 1.340
229
FTT001 Fatty Liver Disease 61 1.340
230
MLD018 Mild Cognitive Impairment 48 1.331
231
BNR002 Bone Resorption Disease 47 1.331
232
HYP066 Hyperglycemia 60 1.331
233
P PRD008 Periodontitis 64 1.331
234
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.326
235
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 1.326
236
P BCL017 B-Cell Lymphoma 57 1.326
237
P THR014 Thrombocytopenia 66 1.321
238
DRG003 Drug Dependence 46 1.310
239
P CRN300 Coronary Heart Disease 1 73 1.308
240
ADR040 Adrenal Gland Pheochromocytoma 45 1.299
241
P PHC003 Pheochromocytoma 70 1.299
242
P RHN004 Rhinitis 57 1.299
244
BRN004 Brain Edema 54 1.288
245
GST023 Gastric Ulcer 52 1.288
246
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.276
247
P LNG028 Long Qt Syndrome 63 1.253
248
PPL052 Papillomatosis, Confluent and Reticulated 34 1.240
249
P FRG001 Fragile X Syndrome 70 1.237
250
P CND004 Candidiasis 57 1.227
251
P RTT002 Rett Syndrome 79 1.214
252
c CHR684 Chronic Kidney Disease 74 1.207
253
PRP007 Priapism 46 1.200
254
NRL004 Neuroleptic Malignant Syndrome 52 1.191
255
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.186
256
AMN001 Amenorrhea 53 1.186
257
GLL008 Gilles De La Tourette Syndrome 64 1.172
258
P HPT023 Hepatocellular Carcinoma 95 1.172
259
BRK010 Burkitt Lymphoma 66 1.172
260
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.171
261
DPS001 Dipsogenic Diabetes Insipidus 21 1.169
262
GLC096 Galactorrhea 40 1.156
263
P HYP098 Hypereosinophilic Syndrome 66 1.156
264
CLT003 Colitis 63 1.150
265
HYP060 Hyperinsulinism 53 1.146
266
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.146
267
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.143
268
P ALP008 Alopecia 53 1.140
269
P ANG015 Angioedema 56 1.123
270
P HRP006 Herpes Simplex 65 1.123
271
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.104
272
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.103
273
P PRP019 Peripheral Nervous System Disease 57 1.091
274
P HYP750 Hypertriglyceridemia, Familial 62 1.086
275
MCR013 Microphthalmia 60 1.079
276
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.079
277
MRP001 Morphine Dependence 41 1.079
278
GST045 Gastroenteritis 58 1.079
279
P NTR004 Neutropenia 62 1.066
280
P VSC011 Vasculitis 61 1.066
281
c PRD040 Periodontitis, Chronic 52 1.052
282
c ATR087 Atrial Standstill 1 74 1.052
283
ERY003 Erythema Multiforme 56 1.052
284
SVR097 Severe Cutaneous Adverse Reaction 68 1.052
285
P GLM040 Glioma Susceptibility 1 70 1.052
286
MLG169 Malignant Astrocytoma 57 1.052
287
GST040 Gastric Adenocarcinoma 66 1.052
288
ALL014 Allergic Encephalomyelitis 34 1.052
289
ERY066 Erythema Multiforme Major 29 1.052
290
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.052
291
c MYS059 Myasthenic Syndrome, Congenital, 4a, Slow-Channel 33 1.051
292
c ACT071 Acute Kidney Failure 60 1.039
293
ADN027 Adenomyosis 59 1.037
294
ORL005 Oral Candidiasis 55 1.037
295
MYL001 Myelitis 49 1.037
296
ACT231 Acute Flaccid Myelitis 16 1.037
297
APH002 Aphasia 55 1.027
298
P RST001 Restless Legs Syndrome 52 1.023
299
P DRM053 Dermatitis, Atopic 65 1.023
300
CRD132 Cardiac Conduction Defect 59 1.023
301
AMN003 Amnestic Disorder 54 1.023
302
P PRP029 Porphyria 60 1.019
303
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 1.007
304
P MYS003 Myasthenia Gravis 68 0.991
305
P MGR001 Migraine Without Aura 48 0.991
307
c PRM108 Primary Progressive Multiple Sclerosis 51 0.974
308
CHL068 Cholestasis 61 0.974
309
SPN027 Spinal Stenosis 59 0.974
310
INT066 Interstitial Lung Disease 60 0.974
311
LNG099 Lung Disease 62 0.974
312
P HYP086 Hypothyroidism 69 0.956
313
P MYS047 Myasthenic Syndrome, Congenital, 1b, Fast-Channel 37 0.947
314
GLB002 Glioblastoma 67 0.945
315
LFT001 Left Bundle Branch Hemiblock 47 0.938
316
PHB003 Phobia, Specific 44 0.938
317
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.938
318
MTR086 Motor Stereotypies 14 0.938
319
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.923
320
P MYS005 Myositis 56 0.917
321
SPS134 Spasmodic Dystonia 28 0.917
322
SPS016 Spasmodic Dysphonia 31 0.917
323
c FNC043 Fanconi Anemia, Complementation Group E 62 0.910
324
ATX019 Ataxia with Vitamin E Deficiency 44 0.910
325
PRT037 Pertussis 49 0.897
326
ATN005 Autonomic Dysfunction 45 0.895
327
P HYP076 Hyperthyroidism 53 0.895
328
P NRC002 Narcolepsy 55 0.885
329
P NRP001 Neuropathy 59 0.871
330
P ORT004 Orthostatic Intolerance 62 0.870
331
TTZ003 Tietz Albinism-Deafness Syndrome 59 0.859
332
P KHL003 Kohlschutter-Tonz Syndrome 57 0.859
333
P INT260 Intracranial Berry Aneurysm 39 0.859
334
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.859
335
HNT002 Hantavirus Pulmonary Syndrome 55 0.859
336
ART002 Arts Syndrome 66 0.859
337
ANR040 Aneurysm 60 0.859
338
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.859
339
CHL079 Children's Interstitial Lung Disease 26 0.859
340
MCR017 Macrocytic Anemia 44 0.858
341
P HYP265 Hypotonia 42 0.858
342
ALL003 Allergic Rhinitis 66 0.844
343
c MYS062 Myasthenic Syndrome, Congenital, 2a, Slow-Channel 28 0.843
344
c MYS048 Myasthenic Syndrome, Congenital, 3a, Slow-Channel 35 0.843
345
c MYS049 Myasthenic Syndrome, Congenital, 3b, Fast-Channel 23 0.843
346
c MYS060 Myasthenic Syndrome, Congenital, 4b, Fast-Channel 26 0.843
347
P ANG001 Angelman Syndrome 65 0.842
348
PRP083 Porphyria, Acute Intermittent 64 0.842
349
P MGR003 Migraine with Aura 51 0.842
350
GYN001 Gynecomastia 48 0.842
351
INF021 Infant Gynecomastia 30 0.842
352
c HYP836 Hypercholesterolemia, Familial, 1 73 0.829
353
CYN002 Cyanosis, Transient Neonatal 43 0.829
354
PRN009 Paranoid Schizophrenia 49 0.829
355
CRN017 Coronary Thrombosis 46 0.829
356
PRS063 Paresthesia 39 0.829
357
BLD053 Blood Platelet Disease 51 0.813
358
SMP001 Simple Partial Epilepsy 8 0.813
359
RMS001 Rem Sleep Behavior Disorder 47 0.813
360
ORL011 Oral Cancer 60 0.813
361
P PRM227 Primary Orthostatic Hypotension 23 0.813
362
P MYC007 Myocardial Infarction 69 0.797
363
P CLR023 Colorectal Cancer 100 0.797
364
P VNT002 Ventricular Septal Defect 58 0.797
365
PLM010 Pulmonary Edema 54 0.797
366
MCL057 Macular Dystrophy with Central Cone Involvement 28 0.797
367
P BRS047 Breast Cancer 97 0.780
368
c CHR708 Chronic Urticaria 42 0.780
369
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.780
370
DYS073 Dysphagia 53 0.780
371
STM007 Stomatitis 52 0.780
372
WHP002 Whiplash 35 0.780
373
MYC006 Mycosis Fungoides 65 0.766
374
P TRT019 Torticollis 47 0.763
375
SCH011 Schizotypal Personality Disorder 36 0.763
376
ATH013 Atherosclerosis Susceptibility 63 0.763
377
c HPT073 Hepatitis C Virus 71 0.763
378
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.763
379
P PLY019 Polyneuropathy 53 0.763
380
c HPT001 Hepatitis C 61 0.763
381
HYP080 Hypogonadism 49 0.763
382
TXC005 Toxic Shock Syndrome 62 0.763
383
DSS009 Disseminated Intravascular Coagulation 56 0.763
384
P PLY011 Polycystic Ovary Syndrome 57 0.763
385
SDD001 Sudden Infant Death Syndrome 60 0.763
386
BRN056 Bronchopulmonary Dysplasia 57 0.763
387
PRT036 Peritonitis 65 0.763
388
GST050 Gastrointestinal System Disease 55 0.763
389
P MYT002 Myotonic Dystrophy 51 0.763
390
P CHN012 Chondrosarcoma 56 0.744
391
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.744
392
BCT022 Bacterial Infectious Disease 56 0.744
393
BRT055 Breath-Holding Spells 26 0.744
394
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.744
395
P HMN032 Human Herpesvirus 8 47 0.744
396
RBS001 Rabies 58 0.744
397
P HYP009 Hypertrophic Pyloric Stenosis 41 0.744
398
PYL006 Pyloric Stenosis 48 0.744
399
DBT004 Diabetic Polyneuropathy 50 0.744
400
RTR008 Root Resorption 44 0.744
401
BRN009 Burning Mouth Syndrome 51 0.744
402
OST012 Osteoarthritis 77 0.744
403
P AMY004 Amyloidosis 69 0.744
404
ILS001 Ileus 49 0.744
405
PRL008 Paralytic Ileus 44 0.744
406
P ENC004 Encephalitis 61 0.744
407
MRG003 Marginal Zone B-Cell Lymphoma 52 0.723
408
c CHR056 Chronic Tic Disorder 36 0.723
409
CLF027 Cleft Palate, Isolated 64 0.723
410
ANS004 Anisometropia 31 0.723
411
LVR012 Liver Cirrhosis 62 0.723
412
HYP014 Hyperuricemia 51 0.723
413
QDR001 Quadriplegia 49 0.723
414
P DDN001 Duodenal Ulcer 53 0.723
415
P MLN007 Male Infertility 56 0.723
416
PRM236 Primary Biliary Cholangitis 62 0.723
417
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.723
418
LRN003 Learning Disability 49 0.723
419
ANG054 Angina Pectoris 65 0.718
420
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.701
421
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.701
422
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.701
423
PCK003 Pick Disease of Brain 69 0.701
424
AGM019 Agammaglobulinemia, X-Linked 72 0.701
425
LWC001 Low Compliance Bladder 44 0.701
426
GT001 Gout 63 0.701
427
P ACN011 Acne 55 0.701
428
P BLP003 Blepharospasm 45 0.701
429
P LTR001 Lateral Sclerosis 58 0.701
430
P AGM001 Agammaglobulinemia 67 0.701
431
HRT011 Heart Septal Defect 49 0.701
432
P PYL005 Pyelonephritis 56 0.701
433
P LVR013 Liver Disease 68 0.701
434
KLP001 Kleptomania 35 0.701
435
P HYP077 Hypertrichosis 48 0.701
436
PHR003 Pharyngitis 57 0.701
437
PRD002 Periodic Limb Movement Disorder 33 0.701
438
DDN027 Duodenum Disease 36 0.701
439
HYP264 Hypertonia 36 0.701
440
BRK012 Broken Heart Syndrome 42 0.701
441
PPT005 Peptic Ulcer Disease 58 0.701
442
ALL006 Allergic Asthma 56 0.701
443
P PST059 Pustular Psoriasis 37 0.701
444
PST062 Pustulosis Palmaris Et Plantaris 46 0.701
445
c CHR692 Chronic Encephalitis 17 0.701
446
P AST005 Asthma 76 0.676
447
P HYP730 Hypogonadotropic Hypogonadism 54 0.676
448
MCS002 Mucositis 55 0.676
449
HYP767 Hyperlexia 20 0.676
450
ORM002 Oromandibular Dystonia 41 0.676
451
CHL065 Cholangiocarcinoma 58 0.676
452
CRD223 Cardiac Arrhythmia 63 0.676
453
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.676
454
AMP007 Amphetamine Abuse 36 0.676
455
INT079 Intrahepatic Cholangiocarcinoma 51 0.676
456
P GLL022 Guillain-Barre Syndrome 59 0.676
457
PRS047 Prostatitis 58 0.676
458
RST023 Resting Heart Rate, Variation in 40 0.676
459
IDP031 Idiopathic Hypersomnia 39 0.676
460
P MSC003 Muscular Atrophy 52 0.676
461
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.676
462
c ACT134 Acute Liver Failure 57 0.676
463
P MCH002 Machado-Joseph Disease 63 0.649
464
ADR016 Adrenal Cortical Carcinoma 61 0.649
465
HMD003 Hemidystonia 28 0.649
466
HMF006 Hemifacial Microsomia 55 0.649
467
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.649
468
DTR001 Detrusor Sphincter Dyssynergia 37 0.649
469
VSM001 Vasomotor Rhinitis 38 0.649
470
HRY002 Hairy Tongue 28 0.649
471
TTN003 Tetanus 64 0.649
472
P SKN015 Skin Carcinoma 71 0.649
473
ADR004 Adrenal Cortical Adenocarcinoma 38 0.649
474
MSC157 Muscular Dystrophy, Duchenne Type 79 0.649
475
PRP030 Purpura 54 0.649
476
CRC021 Carcinosarcoma 62 0.649
477
HDN002 Head Injury 44 0.649
478
SPN050 Spinocerebellar Degeneration 39 0.649
479
DLS001 Delusional Disorder 44 0.649
480
P MSC005 Muscular Dystrophy 66 0.649
481
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.649
482
CRN051 Craniofacial Microsomia 28 0.649
483
PRX097 Paroxysmal Dystonia 32 0.649
484
MCR103 Microtia 40 0.649
485
HYP030 Hypoactive Sexual Desire Disorder 39 0.631
486
DFF005 Diffuse Large B-Cell Lymphoma 55 0.615
487
MNT001 Mantle Cell Lymphoma 65 0.615
488
P GRF003 Graft-Versus-Host Disease 71 0.615
489
APN008 Apnea, Obstructive Sleep 66 0.615
490
c DWL002 Dowling-Degos Disease 1 58 0.615
491
MNN009 Meningoencephalitis 48 0.615
492
VLV011 Vulvovaginal Candidiasis 49 0.615
493
P RTN022 Retinal Vein Occlusion 54 0.615
494
ERL001 Early Myoclonic Encephalopathy 63 0.615
495
TRN015 Transient Cerebral Ischemia 62 0.615
496
OST159 Osteogenic Sarcoma 66 0.615
497
DRV001 Dravet Syndrome 70 0.615
498
P DYS021 Dysautonomia 38 0.615
499
PTH003 Pathologic Nystagmus 52 0.615
500
c BCT007 Bacterial Meningitis 55 0.615
501
c ACT135 Acute Graft Versus Host Disease 51 0.615
502
CRD137 Cardiogenic Shock 56 0.615
503
P CRN037 Craniosynostosis 67 0.604
504
PRS129 Prostatic Hyperplasia, Benign 48 0.572
505
P GST053 Gastric Cancer 82 0.572
506
WST005 West Nile Virus 55 0.572
507
P DNG005 Dengue Virus 55 0.572
508
PHN011 Phenytoin Toxicity 32 0.572
509
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.572
510
P MDL005 Medulloblastoma 75 0.572
511
CRB011 Cerebrotendinous Xanthomatosis 65 0.572
512
MTH071 Methane Production 25 0.572
513
TRG002 Trigeminal Neuralgia 61 0.572
514
P HYP097 Hyperekplexia 62 0.572
515
P FLL037 Follicular Lymphoma 73 0.572
516
XNT003 Xanthomatosis 48 0.572
517
ACT088 Acute Insulin Response 39 0.572
518
ATR057 Atrioventricular Block 54 0.572
519
FTS001 Fetishism 28 0.572
520
PRS021 Prostatic Adenoma 43 0.572
521
PRS045 Prostatic Hypertrophy 52 0.572
522
DNG003 Dengue Disease 65 0.572
523
DNG002 Dengue Hemorrhagic Fever 59 0.572
524
JPN002 Japanese Encephalitis 61 0.572
525
P RHB003 Rhabdomyosarcoma 66 0.572
526
VCC001 Vaccinia 49 0.572
527
OVR094 Ovarian Epithelial Cancer 39 0.572
528
EXT034 Extrinsic Allergic Alveolitis 56 0.572
529
CGT001 Ciguatera Fish Poisoning 20 0.572
530
P MNN013 Meningitis 65 0.572
531
c SPR097 Sporadic Hyperekplexia 12 0.572
532
PNM013 Pneumococcal Meningitis 43 0.572
533
ART140 Arteries, Anomalies of 52 0.527
534
VLC001 Velocardiofacial Syndrome 57 0.527
535
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 0.527
536
LPP008 Lipoprotein Quantitative Trait Locus 65 0.527
537
CYC008 Cyclic Vomiting Syndrome 46 0.468
538
PMP014 Pemphigoid 49 0.468
539
P SCK002 Sick Sinus Syndrome 55 0.468
540
BRS064 Bursitis 51 0.468
541
FRZ001 Frozen Shoulder 54 0.468
542
PDP001 Pedophilia 29 0.468
543
EXH001 Exhibitionism 25 0.468
544
VYR001 Voyeurism 21 0.468
545
BLL006 Bullous Pemphigoid 61 0.468
546
CRT056 Carotidynia 14 0.468
547
CRC006 Carcinoid Syndrome 55 0.468
548
P MLG056 Malignant Hyperthermia 65 0.468
549
ORG003 Organic Mood Syndrome 13 0.468
550
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.442
551
MRD002 Marden-Walker Syndrome 56 0.423
552
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.423
553
c DRR009 Diarrhea 6 46 0.423
554
MRF001 Marfan Syndrome 76 0.423
555
P TRC086 Trichohepatoenteric Syndrome 1 60 0.423
556
IMM167 Immune Deficiency Disease 77 0.423
557
GBM001 Gaba Aminotransferase Deficiency 30 0.423
558
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.423
559
ANG049 Angioedema Induced by Ace Inhibitors 39 0.423
560
DGR001 Digeorge Syndrome 62 0.423
561
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.423
562
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.423
563
WLL001 Williams-Beuren Syndrome 60 0.423
564
RDN001 Reading Disorder 40 0.423
565
PRD004 Prediabetes Syndrome 52 0.423
566
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.423
567
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.423
568
P PTS002 Ptosis 52 0.403
569
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.345
570
P PNC035 Pancreatic Cancer 86 0.329
571
c SCL052 Scleroderma, Familial Progressive 60 0.312
572
c DLT002 Dilated Cardiomyopathy 79 0.312
573
SPS057 Spasticity 43 0.312
574
CHR178 Chromosomal Triplication 34 0.312
575
PLY150 Polykaryocytosis Inducer 29 0.294
576
CHR074 Choriocarcinoma 46 0.294
577
HRT012 Heart Valve Disease 53 0.294
578
HYP005 Hypokalemia 55 0.294
579
ATM095 Autoimmune Disease 61 0.275
580
PST053 Postherpetic Neuralgia 40 0.275
581
GRN017 Granulocytopenia 42 0.275
582
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.255
583
P FML011 Familial Adenomatous Polyposis 71 0.255
584
TST014 Testicular Cancer 51 0.255
585
P FBR017 Fibrosarcoma 55 0.255
587
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.233
588
c PCH010 Pachyonychia Congenita 3 43 0.233
589
ALX002 Alexithymia 37 0.233
590
NRL016 Neural Tube Defects 81 0.233
591
ADJ001 Adjustment Disorder 46 0.233
592
P SYS005 Systemic Scleroderma 73 0.233
593
ACT058 Active Peptic Ulcer Disease 55 0.233
594
c BRN108 Branchiootic Syndrome 1 63 0.208
595
HMC014 Homocysteinemia 52 0.208
596
FRN006 Frontotemporal Dementia 68 0.208
597
P FTL001 Fetal Alcohol Syndrome 55 0.208
598
GST009 Gastroschisis 53 0.208
599
OPP004 Oppositional Defiant Disorder 48 0.208
600
MTN003 Motion Sickness 50 0.208
601
ANN002 Anencephaly 57 0.208
602
P URN019 Urinary Tract Infection 49 0.208
603
PRP027 Peripheral Vascular Disease 71 0.208
604
PLC006 Placental Choriocarcinoma 38 0.208
605
OPD006 Opioid Addiction 48 0.208
606
ABD010 Abdominal Wall Defect 39 0.208
607
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.208
608
c GLL024 Gallbladder Disease 1 53 0.180
609
HLX001 Helix Syndrome 47 0.180
610
FTL006 Fetal Alcohol Spectrum Disorder 43 0.180
611
GLC106 Glucocorticoid Resistance, Generalized 48 0.180
612
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.180
613
CHR710 Chronic Spontaneous Urticaria 45 0.180
614
XRP001 Xerophthalmia 42 0.180
615
MTB004 Metabolic Acidosis 48 0.180
616
OCL066 Oculogyric Crisis 34 0.180
617
DMN031 Dementia, Lewy Body 65 0.180
618
P SJG008 Sjogren Syndrome 61 0.180
619
HPT004 Hepatic Coma 43 0.180
620
ANT011 Antisocial Personality Disorder 47 0.180
621
P OMP004 Omphalocele 47 0.180
622
KRT001 Keratoconjunctivitis Sicca 49 0.180
623
CNG034 Congestive Heart Failure 69 0.180
624
ENT004 Enthesopathy 51 0.180
625
CHL067 Cholecystitis 59 0.180
626
BRN028 Brain Cancer 73 0.180
627
HPT019 Hepatic Encephalopathy 59 0.180
628
PLR008 Pleurisy 49 0.180
629
HST001 Histrionic Personality Disorder 27 0.180
630
P MYC008 Myocarditis 59 0.180
631
P MYP004 Myopathy 67 0.180
632
c ACT075 Acute Myocardial Infarction 55 0.180
633
SCN067 Scn1a Seizure Disorders 13 0.180
634
PRS120 Persistent Idiopathic Facial Pain 27 0.180
635
P BLD134 Bladder Cancer 79 0.147
636
CYS001 Cystic Fibrosis 77 0.147
637
INS024 Insulin-Like Growth Factor I 77 0.147
638
P OCL002 Oculocutaneous Albinism 59 0.147
639
P LYM118 Lymphoma 69 0.147
640
BSL009 Basal Ganglia Calcification 45 0.147
641
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 32 0.147
642
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.147
643
DSC013 Discrimination, Two-Point, Reduction in 21 0.147
644
c DMN023 Diamond-Blackfan Anemia 1 68 0.147
645
OST117 Osteomesopyknosis 23 0.147
646
MLT152 Multiple Self-Healing Squamous Epithelioma 45 0.147
647
LTN004 Late-Onset Retinal Degeneration 60 0.147
648
BRN045 Brunner Syndrome 52 0.147
649
STF001 Stiff-Person Syndrome 57 0.147
650
DSS010 Dissociative Disorder 39 0.147
651
SCH004 Schizoid Personality Disorder 27 0.147
652
PRN010 Paranoid Personality Disorder 26 0.147
653
NRT004 Neuritis 53 0.147
654
CLC006 Calcinosis 47 0.147
655
P ACT028 Acute Closed-Angle Glaucoma 32 0.147
656
CLB002 Clubfoot 51 0.147
657
MNN017 Mononeuropathy 41 0.147
658
CHL014 Cholera 62 0.147
659
PNC001 Pancytopenia 52 0.147
660
c ACT068 Acute Cystitis 61 0.147
661
P END044 Endometriosis 62 0.147
662
CNN005 Connective Tissue Disease 66 0.147
663
ACT038 Acute Retrobulbar Neuritis 24 0.147
664
FCT008 Factitious Disorder 34 0.147
665
PCD001 Pica Disease 38 0.147
666
CNN003 Conn's Syndrome 77 0.147
667
GST037 Gastroparesis 52 0.147
668
SKN016 Skin Disease 62 0.147
669
INT002 Intermittent Claudication 61 0.147
670
P GLL018 Gallbladder Cancer 53 0.147
671
PHN003 Phenylketonuria 76 0.147
672
P CRB088 Cerebral Atrophy 33 0.147
673
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.147
674
c FML191 Familial Long Qt Syndrome 54 0.147
675
P DYS005 Dyslexia 40 0.147
676
P BRT004 Bartter Disease 58 0.147
677
HPT022 Hepatoblastoma 54 0.147
678
INT007 Intermediate Coronary Syndrome 53 0.147
679
P LPS004 Lupus Erythematosus 61 0.147
680
P LPC002 Lip Cancer 45 0.147
681
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.147
682
PLC008 Placenta Disease 49 0.147
683
ALB002 Albinism 47 0.147
684
c LKM005 Leukemia, T-Cell, Chronic 33 0.147
685
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.147
686
PST092 Posttransplant Acute Limbic Encephalitis 29 0.147
687
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.147
688
NNN031 Non-Inflammatory Vasculopathy 6 0.147
689
BNG077 Benign Idiopathic Neonatal Seizures 22 0.147
690
P PRS040 Prostate Cancer 95 0.104
691
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.104
692
HLC007 Helicobacter Pylori Infection 67 0.104
693
FRY006 Fryns Microphthalmia Syndrome 52 0.104
694
MYX004 Myxedema 43 0.104
695
OBS037 Obesity-Hypoventilation Syndrome 44 0.104
696
CFF002 Coffin-Lowry Syndrome 59 0.104
697
c SCH051 Schizophrenia 4 35 0.104
698
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.104
699
P EPL198 Epilepsy, Myoclonic Juvenile 61 0.104
700
WLF001 Wolff-Parkinson-White Syndrome 63 0.104
701
CHR590 Chromosome 15q11-Q13 Duplication Syndrome 35 0.104
702
MYS061 Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency 50 0.104
703
P LKM062 Leukemia, Acute Lymphoblastic 69 0.104
704
c PNC068 Panic Disorder 3 12 0.104
705
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.104
706
DLY008 Delayed Sleep Phase Disorder 44 0.104
707
MYL009 Myelodysplastic Syndrome 67 0.104
708
c DVL072 Developmental and Epileptic Encephalopathy 47 25 0.104
709
PRT251 Proteinuria, Chronic Benign 58 0.104
710
P DST002 Distal Arthrogryposis 63 0.104
711
ATS010 Autosomal Recessive Disease 42 0.104
713
P INF037 Inflammatory Bowel Disease 53 0.104
714
c PRC016 Pre-Eclampsia 64 0.104
715
INT395 Intracranial Meningioma 48 0.104
716
TNS005 Tonsillitis 57 0.104
717
ACR062 Acroosteolysis 33 0.104
718
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.104
719
c FNC027 Fanconi Anemia, Complementation Group a 81 0.104
720
P LPR021 Leprosy 3 71 0.104
721
P CLC063 Celiac Disease 1 66 0.104
722
CRN264 Craniosynostosis with Fibular Aplasia 29 0.104
723
P CTN015 Cutaneous T Cell Lymphoma 48 0.104
724
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.104
725
P BRG001 Brugada Syndrome 69 0.104
727
VTM002 Vitamin B12 Deficiency 48 0.104
728
PNC085 Penicillin Allergy 43 0.104
729
CRV043 Cervical Dystonia 45 0.104
730
CHL147 Chlamydia Pneumonia 47 0.104
731
ANS006 Anosognosia 34 0.104
732
P MYC084 Mycobacterium Tuberculosis 1 68 0.104
733
P APL001 Aplastic Anemia 73 0.104
735
THY064 Thyroid Hormone Metabolism, Abnormal 28 0.104
736
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.104
737
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.104
738
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.104
739
THY069 Thyroid Hormone Resistance, Selective Pituitary 36 0.104
740
MLK003 Melkersson-Rosenthal Syndrome 43 0.104
741
PMP006 Pemphigus Vulgaris, Familial 58 0.104
742
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 0.104
743
SMT004 Smith-Lemli-Opitz Syndrome 69 0.104
744
DPN001 Dependent Personality Disorder 26 0.104
745
c SCH079 Schizophrenia 1 44 0.104
746
P TTR001 Tetralogy of Fallot 69 0.104
747
P BNC003 Bone Cancer 58 0.104
748
DYS004 Dyscalculia 35 0.104
749
P BND020 Bone Disease 60 0.104
750
P MYG005 Myoglobinuria 40 0.104
751
LYM040 Lymphoblastic Lymphoma 53 0.104
752
DFC004 Deficiency Anemia 74 0.104
753
BRN014 Bronchopneumonia 52 0.104
754
c FML021 Familial Hypercholesterolemia 71 0.104
755
PTH002 Pathological Gambling 48 0.104
756
P TBR001 Tuberous Sclerosis 69 0.104
757
CMP010 Complex Regional Pain Syndrome 59 0.104
758
CNT047 Contact Dermatitis 57 0.104
759
P MTR012 Mitral Valve Disease 57 0.104
760
ADS003 Aids Phobia 20 0.104
761
BRN018 Borna Disease 36 0.104
762
PLM031 Poliomyelitis 62 0.104
763
P MCR010 Microcephaly 59 0.104
764
P ATR010 Atrial Heart Septal Defect 58 0.104
765
c ATM011 Autoimmune Hepatitis 62 0.104
766
P HMN010 Hemangioma 61 0.104
767
CNT016 Central Retinal Vein Occlusion 54 0.104
768
FCL012 Facial Paralysis 49 0.104
769
P INT143 Interstitial Cystitis 59 0.104
770
GLS004 Glossopharyngeal Neuralgia 37 0.104
771
CRB033 Cerebral Degeneration 36 0.104
772
LYM022 Lymphangioma 54 0.104
773
P CYS018 Cystitis 59 0.104
774
P HYD006 Hydrocephalus 63 0.104
775
ANG005 Anogenital Venereal Wart 55 0.104
776
CHL123 Chlamydia 58 0.104
777
P HYP061 Hypertrophic Cardiomyopathy 69 0.104
778
ASP003 Aseptic Meningitis 51 0.104
779
CHG001 Chagas Disease 65 0.104
780
NRG002 Neurogenic Bladder 55 0.104
781
ATN004 Autonomic Neuropathy 42 0.104
782
ALL010 Allergic Contact Dermatitis 56 0.104
783
c TRN005 Transient Tic Disorder 17 0.104
784
P VNW001 Von Willebrand's Disease 64 0.104
785
c ACT076 Acute Myocarditis 47 0.104
786
EMB004 Embryonal Carcinoma 55 0.104
787
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.104
788
c RTN047 Retinitis Pigmentosa 18 45 0.104
789
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.104
790
MNN043 Meningioma, Familial 79 0.104
791
MST020 Mast Cell Activation Syndrome 27 0.104
792
P RRL003 Rare Lymphatic Malformation 31 0.104
793
SPC005 Speech Disorder 46 0.104
794
P CTR002 Cataract 59 0.104
795
NNT008 Neonatal Abstinence Syndrome 40 0.104
796
CLF001 Cleft Lip 54 0.104
797
P PNM007 Pneumonia 64 0.104
798
RTR001 Retrograde Amnesia 41 0.104
799
SCR001 Secretory Meningioma 40 0.104
800
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.104
801
P RBL001 Rubella 58 0.104
802
DYS003 Dysgraphia 35 0.104
803
FLP002 Floppy Infant Syndrome 13 0.104
804
P CRB059 Cerebellar Degeneration 36 0.104
805
P CHR342 Chiari Malformation 41 0.104
806
NRT002 Neurotic Excoriation 31 0.104
807
P RTN016 Retinal Degeneration 52 0.104
808
DVR002 Diverticulitis 46 0.104
809
INH003 Inhibited Female Orgasm 28 0.104
810
ULC004 Ulcerative Colitis 74 0.104
811
CRB017 Cerebral Falx Meningioma 25 0.104
812
HRN003 Heroin Dependence 44 0.104
814
RCR002 Recurrent Hypersomnia 27 0.104
815
CRN088 Craniorachischisis 35 0.104
816
HMC012 Hemicrania Continua 26 0.104
817
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 0.104
818
CHR281 Chronic Hiccups 28 0.104
819
CNG113 Congenital Myasthenic Syndrome Associated with Acetylcholine Receptor Deficiency 22 0.104
820
KR001 Koro 18 0.104
821
P DBT005 Diabetes Insipidus 54 0.104
822
HNS001 Hansen's Disease 32 0.104
823
HYP144 Hyperacusis 23 0.104
824
HYP835 Hypothalamic Obesity 38 0.104
825
LYM019 Lymphosarcoma 46 0.104
826
NWD001 New Daily-Persistent Headache 19 0.104
827
FLL019 Follicular Mucinosis 31 0.104
828
GRN059 Grn Frontotemporal Dementia 16 0.104
829
P PMP001 Pemphigus 55 0.104
830
SYR007 Syringohydromyelia 15 0.104
831
SPC030 Specific Language Disorder 25 0.104
832
PST103 Postpartum Psychosis 31 0.104
833
CNG506 Congenital Amyoplasia 27 0.104
834
RRM016 Rare Movement Disorder 15 0.104
835
CCN009 Cocaine Intoxication 29 0.104
836
RNL078 Renal Dysplasia 46 0.104
837
P OVR082 Overgrowth Syndrome 42 0.104
838
MTR087 Maternal Uniparental Disomy 27 0.104
839
URM005 Uremic Pruritus 45 0.104
840
THY029 Thyroid Carcinoma 54 0.104
Content
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