Search results for Methylphenidate

658 hits were found for Methylphenidate

# Family MCID Name MIFTS Score
1
P ATT013 Attention Deficit-Hyperactivity Disorder 66 44.129
2
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 11.736
3
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 10.454
4
P NRC002 Narcolepsy 55 8.271
5
BRN071 Brain Injury 50 7.511
6
TRM010 Traumatic Brain Injury 50 7.450
7
P SBS003 Substance Abuse 54 7.087
8
MNT002 Mental Depression 56 6.162
9
CND002 Conduct Disorder 50 5.986
10
P PRS038 Personality Disorder 65 5.772
11
CCN002 Cocaine Abuse 49 5.737
12
ANX010 Anxiety 70 5.715
13
DPR016 Depression 65 5.613
14
P ATS364 Autism 72 5.569
15
CCN001 Cocaine Dependence 48 5.174
16
P EPL164 Epilepsy 70 5.161
17
c MJR024 Major Affective Disorder 9 40 5.133
18
c MJR022 Major Affective Disorder 8 37 5.133
19
P BPL003 Bipolar Disorder 56 5.133
20
c ATS007 Autism Spectrum Disorder 72 4.890
21
OPP004 Oppositional Defiant Disorder 48 4.847
22
P TCD001 Tic Disorder 50 4.843
23
P PRK057 Parkinson Disease, Late-Onset 79 4.806
24
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.727
25
MDD011 Mood Disorder 62 4.579
26
PSY004 Psychotic Disorder 66 4.454
27
P SZR006 Seizure Disorder 69 4.441
28
P SLP005 Sleep Disorder 62 4.399
29
P PRV006 Pervasive Developmental Disorder 52 4.386
30
ADL002 Adult Syndrome 69 4.216
31
AGN016 Aging 54 4.200
32
P MJR001 Major Depressive Disorder 68 4.169
33
P DMN002 Dementia 65 4.159
34
P ALZ034 Alzheimer Disease 87 4.135
35
END040 Endogenous Depression 54 4.026
36
P PRK039 Parkinsonism 55 3.879
37
P MLT020 Multiple Sclerosis 79 3.528
38
SBC016 Subacute Delirium 42 3.509
39
P ANR048 Aniridia 1 66 3.501
40
OBS002 Obsessive-Compulsive Disorder 68 3.491
41
MLD018 Mild Cognitive Impairment 48 3.385
42
ETN001 Eating Disorder 59 3.380
43
AVD001 Avoidant Personality Disorder 49 3.324
44
P TRN020 Turner Syndrome 67 3.306
45
P SMK004 Smoking As a Quantitative Trait Locus 3 44 3.282
46
TBC004 Tobacco Addiction 63 3.282
47
P LKM062 Leukemia, Acute Lymphoblastic 69 3.259
48
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 3.203
49
DSS008 Disease of Mental Health 74 3.197
50
PST028 Post-Traumatic Stress Disorder 59 3.178
51
GLL008 Gilles De La Tourette Syndrome 64 3.107
52
AND005 Androgen Insensitivity Syndrome, Mild 21 2.980
53
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.956
54
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.956
55
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.956
56
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.956
57
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.956
58
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.956
59
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.956
60
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.956
61
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.956
62
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.956
63
BRD004 Borderline Personality Disorder 53 2.928
64
CRD132 Cardiac Conduction Defect 59 2.794
65
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.778
66
ALC007 Alcohol Dependence 65 2.729
68
P KHL003 Kohlschutter-Tonz Syndrome 57 2.671
69
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 2.668
70
BLM002 Bulimia Nervosa 57 2.654
71
NRT001 Neurotic Disorder 56 2.634
72
P NRF002 Neurofibromatosis 60 2.631
73
P MYT002 Myotonic Dystrophy 51 2.615
74
P SRC025 Sarcoidosis 1 70 2.537
75
P ALC033 Alcohol Use Disorder 67 2.519
76
CHR066 Chronic Fatigue Syndrome 60 2.483
77
ACQ007 Acquired Immunodeficiency Syndrome 58 2.482
78
LRN003 Learning Disability 49 2.464
79
ALL029 Allergic Disease 61 2.415
80
DWN001 Down Syndrome 70 2.406
81
P CRD119 Cardiac Arrest 68 2.399
82
P MVM001 Movement Disease 61 2.397
83
TRC010 Trichotillomania 50 2.389
84
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 2.323
85
HMN044 Human Immunodeficiency Virus Type 1 76 2.303
86
P TRM003 Tremor 50 2.300
87
RDN001 Reading Disorder 40 2.291
88
DRG003 Drug Dependence 46 2.290
89
VLC001 Velocardiofacial Syndrome 57 2.282
90
EPT021 Epithelial Recurrent Erosion Dystrophy 46 2.279
91
BRN028 Brain Cancer 73 2.279
92
CHL079 Children's Interstitial Lung Disease 26 2.247
93
LPT014 Leptin Deficiency or Dysfunction 77 2.214
94
c NRF024 Neurofibromatosis, Type I 76 2.184
95
DVL001 Developmental Coordination Disorder 34 2.183
96
P DYS154 Dystonia 64 2.182
97
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 2.170
98
P NRV007 Nervous System Disease 66 2.165
99
RHB024 Rhabdomyosarcoma 2 65 2.157
100
ACT084 Acute Stress Disorder 53 2.156
101
OCL069 Ocular Motor Apraxia 57 2.152
102
48X005 48,xyyy 39 2.133
103
SCL003 Social Phobia 48 2.087
104
ART002 Arts Syndrome 66 2.075
105
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.072
106
P PNC025 Panic Disorder 52 2.051
107
PRP007 Priapism 46 2.047
108
WLL001 Williams-Beuren Syndrome 60 2.005
109
P HRT032 Heart Disease 84 1.940
110
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.933
111
OPT003 Opiate Dependence 49 1.907
112
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.897
113
P HYP263 Hypersomnia 40 1.870
114
AMD002 Amed Syndrome, Digenic 37 1.822
115
P MJR007 Major Affective Disorder 1 42 1.810
116
c MJR008 Major Affective Disorder 2 34 1.810
117
CGN007 Cognitive Function 1, Social 26 1.810
118
c MJR006 Major Affective Disorder 5 32 1.810
119
c MJR003 Major Affective Disorder 6 32 1.810
120
c MJR004 Major Affective Disorder 4 28 1.810
121
c MJR023 Major Affective Disorder 7 33 1.810
122
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.810
123
DVL005 Developmental Dyspraxia 22 1.761
124
KLN009 Kleine-Levin Hibernation Syndrome 37 1.758
125
P DYS005 Dyslexia 40 1.733
126
P FRG001 Fragile X Syndrome 70 1.716
127
HDN002 Head Injury 44 1.689
128
ANT011 Antisocial Personality Disorder 47 1.678
129
HNT002 Hantavirus Pulmonary Syndrome 55 1.665
130
CNT033 Central Nervous System Cancer 47 1.665
131
P NRV006 Nervous System Cancer 47 1.665
132
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.665
133
ANR007 Anorexia Nervosa 59 1.640
134
VSC002 Vascular Dementia 59 1.640
135
ANT039 Antisynthetase Syndrome 55 1.635
136
AMN003 Amnestic Disorder 54 1.631
137
OPD001 Opioid Abuse 44 1.630
138
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.619
139
P PRS040 Prostate Cancer 95 1.610
140
P BRG001 Brugada Syndrome 69 1.610
141
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 30 1.610
142
PRS047 Prostatitis 58 1.610
143
NRF007 Neurofibroma 64 1.603
144
HYP005 Hypokalemia 55 1.603
147
47X002 47,xyy 48 1.579
148
CNT047 Contact Dermatitis 57 1.559
149
BRX001 Bruxism 51 1.536
150
P SCH015 Schizophrenia 74 1.525
151
P SCK005 Sickle Cell Disease 56 1.502
152
HYL004 Hyaline Fibromatosis Syndrome 66 1.490
153
ACR041 Acromelic Frontonasal Dysostosis 53 1.490
154
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 1.490
155
LPT006 Leptin Receptor Deficiency 50 1.490
156
PSD088 Pseudobulbar Affect 33 1.488
157
P BRS047 Breast Cancer 97 1.476
158
c MSM022 Mismatch Repair Cancer Syndrome 1 69 1.476
159
c SRC023 Sarcoidosis 2 44 1.476
160
P LYM118 Lymphoma 69 1.476
161
c PRS130 Prostate Cancer, Hereditary, 8 32 1.476
162
c PRS136 Prostate Cancer, Hereditary, 6 33 1.476
163
LYM040 Lymphoblastic Lymphoma 53 1.476
164
P LKM002 Leukemia 66 1.476
165
ADS004 Aids Dementia Complex 40 1.476
166
LYM019 Lymphosarcoma 46 1.476
167
TRD006 Tardive Dyskinesia 53 1.475
168
SYN036 Syncope 44 1.475
169
P ALP008 Alopecia 53 1.471
170
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.460
171
AMP007 Amphetamine Abuse 36 1.460
172
P EXN002 Exanthem 58 1.433
173
P MYC007 Myocardial Infarction 69 1.433
174
RYN005 Raynaud Phenomenon 45 1.433
175
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.418
176
MRF001 Marfan Syndrome 76 1.414
177
CNN001 Cannabis Dependence 38 1.414
178
P SLP006 Sleep Apnea 69 1.392
179
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.387
180
CHR073 Choreatic Disease 53 1.387
181
CRB037 Cerebral Palsy 67 1.371
182
SCH012 Schizoaffective Disorder 49 1.355
183
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.341
184
STT041 Stuttering 52 1.340
185
c ATR087 Atrial Standstill 1 74 1.335
186
c CHR056 Chronic Tic Disorder 36 1.328
187
SBS004 Substance Dependence 46 1.328
188
HND015 Hand Skill, Relative 29 1.315
189
MRD002 Marden-Walker Syndrome 56 1.301
190
HYP458 Hyper Ige Syndrome 60 1.301
191
P FNG006 Feingold Syndrome 1 61 1.301
192
GST071 Gastrointestinal Carcinoma 46 1.301
193
c MYT021 Myotonic Dystrophy 1 67 1.301
194
DGR001 Digeorge Syndrome 62 1.301
195
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 1.301
196
OBS003 Obsessive-Compulsive Personality Disorder 43 1.301
197
GLB002 Glioblastoma 67 1.301
198
AGR002 Agoraphobia 45 1.301
199
MLG023 Malignant Adult Ependymoma 15 1.301
200
ADL054 Adult Brain Stem Glioma 29 1.301
201
P CRN037 Craniosynostosis 67 1.301
202
HMT002 Hematologic Cancer 61 1.301
203
GST049 Gastrointestinal System Cancer 49 1.301
204
ATX019 Ataxia with Vitamin E Deficiency 44 1.301
205
CRH001 Crohn's Disease 80 1.301
206
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.301
207
ADL045 Adult Ependymoblastoma 14 1.301
208
CNN002 Cannabis Abuse 44 1.301
209
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.301
210
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.301
211
CHR682 Chronic Bilirubin Encephalopathy 37 1.301
212
P VSC011 Vasculitis 61 1.300
213
c ACT075 Acute Myocardial Infarction 55 1.295
214
IDP031 Idiopathic Hypersomnia 39 1.245
215
P PLY006 Polydactyly 58 1.237
216
SRT004 Serotonin Syndrome 54 1.222
217
PRT058 Pure Autonomic Failure 58 1.218
218
FRN006 Frontotemporal Dementia 68 1.183
219
STT001 Status Epilepticus 58 1.182
220
CRN019 Coronary Artery Vasospasm 47 1.182
221
STR067 Stroke, Ischemic 79 1.178
222
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 1.170
223
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.161
224
P PLM034 Pulmonary Emphysema 58 1.161
225
DMP001 Dumping Syndrome 43 1.156
226
CRB005 Cerebral Arteritis 28 1.139
227
CRB039 Cerebrovascular Disease 65 1.131
228
P CNJ013 Conjunctivitis 66 1.131
229
P MYC008 Myocarditis 59 1.127
230
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.115
231
P HNT016 Huntington Disease 73 1.111
232
P FTL001 Fetal Alcohol Syndrome 55 1.095
233
FTL006 Fetal Alcohol Spectrum Disorder 43 1.095
234
P HYP086 Hypothyroidism 69 1.095
235
GYN001 Gynecomastia 48 1.089
236
INF021 Infant Gynecomastia 30 1.089
237
c ATT020 Attention Deficit-Hyperactivity Disorder 2 13 1.079
238
PLY068 Polysubstance Abuse 41 1.079
239
P MYC033 Myoclonus 46 1.079
240
P CTR002 Cataract 59 1.079
241
P LNG028 Long Qt Syndrome 63 1.074
242
IMP005 Impotence 52 1.061
243
INS024 Insulin-Like Growth Factor I 77 1.058
244
ALL010 Allergic Contact Dermatitis 56 1.058
245
c BPL002 Bipolar I Disorder 47 1.043
246
CRN036 Craniopharyngioma 63 1.043
247
HYP835 Hypothalamic Obesity 38 1.043
248
P FML340 Familial Episodic Pain Syndrome 50 1.024
249
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.024
251
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.024
252
ASP004 Asphyxia Neonatorum 50 1.024
253
HRT012 Heart Valve Disease 53 1.024
254
c HYP595 Hypertension, Essential 84 1.019
255
ACT011 Acute Contagious Conjunctivitis 42 1.019
256
SCH036 Scheie Syndrome 73 1.019
257
P PLM037 Pulmonary Hypertension 69 1.003
258
P HYD006 Hydrocephalus 63 1.003
259
CLL003 Cellulitis 53 1.003
260
HPT067 Hepatocellular Adenoma 42 0.990
261
HPT022 Hepatoblastoma 54 0.990
262
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.981
263
RST023 Resting Heart Rate, Variation in 40 0.981
264
ATN005 Autonomic Dysfunction 45 0.981
265
P ALP009 Alopecia Areata 59 0.981
266
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.957
267
P BLP003 Blepharospasm 45 0.957
268
P NRM002 Normal Pressure Hydrocephalus 49 0.957
269
MTS001 Mutism 44 0.957
270
NSP002 Nasopharyngitis 45 0.930
271
ADR040 Adrenal Gland Pheochromocytoma 45 0.930
272
P PHC003 Pheochromocytoma 70 0.930
273
HRW001 Hair Whorl 35 0.930
274
PRC013 Pericarditis 53 0.930
275
FCL014 Focal Epilepsy 53 0.930
276
BLP048 Blepharospasm, Benign Essential 36 0.930
277
PNM010 Pneumothorax, Primary Spontaneous 58 0.900
278
CYN002 Cyanosis, Transient Neonatal 43 0.900
279
ISC004 Ischemia 61 0.900
280
SVR004 Severe Combined Immunodeficiency 71 0.900
281
PNM008 Pneumothorax 54 0.900
282
NRL004 Neuroleptic Malignant Syndrome 52 0.900
283
HYP266 Hypoxia 56 0.900
284
P HDC001 Headache 56 0.889
285
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.879
286
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 52 0.879
287
c LNG044 Long Qt Syndrome 1 66 0.879
288
c HMG001 Hemoglobin C Disease 41 0.879
289
P CRD246 Cardiovascular System Disease 55 0.879
290
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.879
291
WTH001 Withdrawal Disorder 47 0.872
292
IRN002 Iron Metabolism Disease 56 0.872
293
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.864
294
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.864
295
c DLT002 Dilated Cardiomyopathy 79 0.864
296
P URT039 Urticaria 57 0.864
297
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.855
298
P NRB001 Neuroblastoma 66 0.855
299
PLM033 Pulmonary Embolism 58 0.855
300
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.844
301
SPR126 Superior Semicircular Canal Dehiscence 41 0.844
302
c ORT011 Orthostatic Hypotension 1 43 0.844
303
HYP781 Hypoascorbemia 52 0.844
304
SCK003 Sickle Cell Anemia 74 0.844
305
DFC004 Deficiency Anemia 74 0.844
306
NTR005 Nutritional Deficiency Disease 60 0.844
307
KRT002 Keratomalacia 54 0.844
308
ALX001 Alexia 44 0.844
309
c HMG029 Hemoglobin Se Disease 41 0.844
310
APH002 Aphasia 55 0.837
311
CRN270 Coronary Artery Dissection, Spontaneous 32 0.817
312
NRL016 Neural Tube Defects 81 0.817
313
HMP005 Hemiplegia 53 0.817
314
P THR014 Thrombocytopenia 66 0.817
315
BRN049 Brain Tumor, Childhood 28 0.817
316
ACR008 Acrocallosal Syndrome 70 0.817
317
AMN014 Aminopterin Syndrome Sine Aminopterin 31 0.817
318
GNR004 Generalized Anxiety Disorder 55 0.817
319
GRN059 Grn Frontotemporal Dementia 16 0.817
320
SXL003 Sexual Disorder 49 0.797
321
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.797
322
P PTS002 Ptosis 52 0.797
323
PTT009 Pituitary Gland Disease 53 0.797
324
P CHR345 Chronic Pain 50 0.797
325
DSS032 Disease by Infectious Agent 55 0.774
326
APR001 Apraxia 51 0.774
327
ALL003 Allergic Rhinitis 66 0.774
328
ADJ001 Adjustment Disorder 46 0.774
329
ANT019 Anterograde Amnesia 38 0.774
330
P RHN004 Rhinitis 57 0.774
331
P ORT004 Orthostatic Intolerance 62 0.774
332
P INF038 Influenza 68 0.774
333
CYC001 Cycloplegia 35 0.750
334
MYL020 Myelomeningocele 51 0.750
335
IMP006 Impulse Control Disorder 45 0.750
336
P CLS010 Cluster Headache 42 0.750
337
P PRC019 Precocious Puberty 49 0.750
338
CYS021 Cystic Adenomatoid Malformation of Lung 32 0.750
339
APR010 Apraxia of Eyelid Opening 15 0.724
340
PRT001 Partial Fetal Alcohol Syndrome 21 0.724
341
PNG002 Pain Agnosia 51 0.724
342
ORM002 Oromandibular Dystonia 41 0.724
343
CNG034 Congestive Heart Failure 69 0.724
344
P INF032 Infertility 60 0.724
345
HGH043 High Grade Glioma 46 0.724
346
ANX004 Anoxia 40 0.724
347
SPS057 Spasticity 43 0.724
348
P HYP098 Hypereosinophilic Syndrome 66 0.724
349
PST092 Posttransplant Acute Limbic Encephalitis 29 0.724
350
FXD003 Fixed Drug Eruption 34 0.724
351
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.724
352
KLP001 Kleptomania 35 0.705
353
ORG003 Organic Mood Syndrome 13 0.705
354
P TRT019 Torticollis 47 0.694
355
c BRN108 Branchiootic Syndrome 1 63 0.694
356
TNS005 Tonsillitis 57 0.694
357
P SCL018 Scoliosis 57 0.694
358
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.694
359
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.694
360
ATM095 Autoimmune Disease 61 0.694
361
P RSP003 Respiratory Failure 74 0.694
362
ENC005 Encephalomalacia 43 0.694
363
SPC010 Speech and Communication Disorders 48 0.694
364
MNN009 Meningoencephalitis 48 0.694
365
P DDN001 Duodenal Ulcer 53 0.694
366
CYT002 Cytokine Deficiency 43 0.694
367
EXT039 Extrapontine Myelinolysis 18 0.694
368
TBR011 Tuberculous Meningitis 48 0.694
369
c CNT075 Central Precocious Puberty 53 0.694
370
NNT008 Neonatal Abstinence Syndrome 40 0.694
371
VRL011 Viral Infectious Disease 60 0.694
372
PTH003 Pathologic Nystagmus 52 0.694
373
P BCL017 B-Cell Lymphoma 57 0.694
374
P ENC004 Encephalitis 61 0.694
375
HRP009 Herpes Simplex Encephalitis 58 0.694
376
ALL001 Allan-Herndon-Dudley Syndrome 54 0.658
377
P ASP001 Asperger Syndrome 48 0.658
379
PHT008 Photosensitive Epilepsy 42 0.658
380
PHB003 Phobia, Specific 44 0.658
381
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.658
382
LWC001 Low Compliance Bladder 44 0.658
383
PRP016 Paraplegia 52 0.658
384
P PNC044 Pancreatitis 61 0.658
385
c ESS001 Essential Tremor 56 0.658
386
DYS009 Dysthymic Disorder 51 0.658
387
EXP001 Expressive Language Disorder 24 0.658
388
GST023 Gastric Ulcer 52 0.658
389
P LVR013 Liver Disease 68 0.658
390
c ACT076 Acute Myocarditis 47 0.658
391
c JVN015 Juvenile Huntington Disease 24 0.658
392
P ENC018 Encephalopathy 62 0.658
393
PRS063 Paresthesia 39 0.658
394
PRD002 Periodic Limb Movement Disorder 33 0.658
395
TRN015 Transient Cerebral Ischemia 62 0.617
396
GLC096 Galactorrhea 40 0.611
398
c ATT019 Attention Deficit-Hyperactivity Disorder 1 11 0.611
399
CRB004 Cerebral Artery Occlusion 46 0.611
400
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.611
401
c CHR711 Chronic Asthma 41 0.611
402
P ANP001 Anaplastic Large Cell Lymphoma 61 0.611
403
IFP003 Ifap Syndrome 2 42 0.611
404
P ADN016 Adenocarcinoma 63 0.611
405
ADN018 Adenoma 58 0.611
406
c VRL007 Viral Encephalitis 50 0.611
407
OVR063 Overnutrition 42 0.611
408
DPR002 Depersonalization Disorder 41 0.611
409
c HRD010 Hereditary Spastic Paraplegia 65 0.611
410
TST015 Testicular Disease 42 0.611
411
RHM001 Rheumatic Fever 59 0.611
412
CNV002 Conversion Disorder 47 0.611
413
IRR003 Irritant Dermatitis 47 0.611
414
NWC001 Newcastle Disease 48 0.611
415
MSC157 Muscular Dystrophy, Duchenne Type 79 0.611
416
P PNC035 Pancreatic Cancer 86 0.611
417
DRM006 Dermatitis 62 0.611
418
PRP030 Purpura 54 0.611
419
P HRP006 Herpes Simplex 65 0.611
420
ACT162 Acute Sensory Ataxic Neuropathy 24 0.611
421
CDK006 Cdkl5 Deficiency Disorder 30 0.611
422
APP008 Appendicitis 62 0.611
423
DLS001 Delusional Disorder 44 0.611
424
HYP056 Hypoglycemia 65 0.611
425
P MSC005 Muscular Dystrophy 66 0.611
426
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 36 0.611
427
CRD137 Cardiogenic Shock 56 0.611
428
TXC002 Toxic Encephalopathy 51 0.535
429
P STS008 Sotos Syndrome 1 62 0.498
430
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.498
431
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.498
432
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.498
433
P ANG015 Angioedema 56 0.498
434
P PRN023 Prion Disease 60 0.498
435
c ATM011 Autoimmune Hepatitis 62 0.498
436
SPL006 Splenic Infarction 37 0.498
437
PCD001 Pica Disease 38 0.498
438
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.498
439
GLM045 Glioma 62 0.498
440
GLL048 Glial Tumor 52 0.498
441
P ART022 Arthritis 70 0.498
442
MSP003 Misophonia 16 0.498
443
CHR281 Chronic Hiccups 28 0.498
444
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.498
445
PST086 Posterior Cortical Atrophy 36 0.498
446
CNS004 Constipation 56 0.437
447
P DBT009 Diabetes Mellitus 67 0.422
448
c PNS012 Paine Syndrome 60 0.422
449
RCK004 Rickets 65 0.422
450
c CRN243 Carney Complex, Type 1 53 0.422
451
MST019 Mastoiditis 41 0.422
452
c MST023 Mesothelioma, Malignant 56 0.422
453
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.422
454
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.422
455
KDN007 Kidney Clear Cell Sarcoma 40 0.422
456
DNT012 Dental Caries 53 0.422
457
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.422
458
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.422
459
P AMY004 Amyloidosis 69 0.422
460
ART109 Arterial Thoracic Outlet Syndrome 24 0.422
461
CYC005 Cyclothymic Disorder 40 0.319
462
c PRC016 Pre-Eclampsia 64 0.298
463
DMN031 Dementia, Lewy Body 65 0.298
464
IMM167 Immune Deficiency Disease 77 0.276
465
PLC007 Placental Abruption 47 0.276
466
c MGR028 Migraine with or Without Aura 1 64 0.252
468
P RTT002 Rett Syndrome 79 0.252
469
P HYP265 Hypotonia 42 0.252
470
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.252
471
P END033 Endocarditis 58 0.226
472
CLB010 Coloboma of Macula 53 0.226
473
PCK003 Pick Disease of Brain 69 0.226
474
c SCL052 Scleroderma, Familial Progressive 60 0.226
475
SPR004 Supravalvular Aortic Stenosis 57 0.226
476
MLT157 Multiple System Atrophy 1 69 0.226
477
PTH002 Pathological Gambling 48 0.226
478
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.226
479
SPC031 Specific Learning Disability 36 0.226
480
P RST001 Restless Legs Syndrome 52 0.195
481
PRP015 Paraphilia Disorder 32 0.195
482
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.195
483
HYP080 Hypogonadism 49 0.195
484
HRT011 Heart Septal Defect 49 0.195
485
P VNT002 Ventricular Septal Defect 58 0.195
486
P HYP061 Hypertrophic Cardiomyopathy 69 0.195
487
HYP043 Hyperandrogenism 47 0.195
488
DYS073 Dysphagia 53 0.195
489
c HRD088 Hereditary Neuropathies 34 0.195
490
RMS001 Rem Sleep Behavior Disorder 47 0.195
491
PLC008 Placenta Disease 49 0.195
492
HRN003 Heroin Dependence 44 0.195
493
RCR002 Recurrent Hypersomnia 27 0.195
494
P MCH002 Machado-Joseph Disease 63 0.159
495
P MYS003 Myasthenia Gravis 68 0.159
496
ANG054 Angina Pectoris 65 0.159
497
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.159
498
c SPN296 Spinocerebellar Ataxia 17 47 0.159
499
MTN003 Motion Sickness 50 0.159
500
P CRN026 Corneal Edema 42 0.159
501
CRD223 Cardiac Arrhythmia 63 0.159
502
P PRD006 Prader-Willi Syndrome 60 0.159
503
SPC001 Space Motion Sickness 26 0.159
504
c HPT001 Hepatitis C 61 0.159
505
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.159
506
CHL012 Childhood Disintegrative Disease 44 0.159
507
SKN016 Skin Disease 62 0.159
508
AKN002 Akinetic Mutism 36 0.159
509
P BNG032 Benign Mesothelioma 53 0.159
510
CRT033 Corticobasal Degeneration 48 0.159
511
INT075 Intracranial Hypertension 52 0.159
512
P PRM227 Primary Orthostatic Hypotension 23 0.159
513
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.159
514
GST092 Gastroesophageal Reflux 60 0.113
515
SCH076 Schnyder Corneal Dystrophy 46 0.113
516
PRS129 Prostatic Hyperplasia, Benign 48 0.113
517
BTT016 Batten-Turner Congenital Myopathy 53 0.113
518
MYL069 Myeloma, Multiple 77 0.113
519
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.113
520
WLS001 Wilson Disease 70 0.113
521
LSC001 Lesch-Nyhan Syndrome 62 0.113
522
CHR590 Chromosome 15q11-Q13 Duplication Syndrome 35 0.113
523
c ATT021 Attention Deficit-Hyperactivity Disorder 3 10 0.113
524
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 55 0.113
525
KWS002 Kawasaki Disease 65 0.113
526
P TMR010 Tumor Predisposition Syndrome 69 0.113
527
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.113
528
P OCL002 Oculocutaneous Albinism 59 0.113
530
P INF037 Inflammatory Bowel Disease 53 0.113
531
PST048 Postural Orthostatic Tachycardia Syndrome 46 0.113
532
GLC003 Glucose Intolerance 53 0.113
533
PRT013 Portal Hypertension 59 0.113
534
P MDL005 Medulloblastoma 75 0.113
535
APN008 Apnea, Obstructive Sleep 66 0.113
536
P RHM011 Rheumatoid Arthritis 81 0.113
537
P CLC063 Celiac Disease 1 66 0.113
538
ALX002 Alexithymia 37 0.113
539
FNG001 Finger Agnosia 19 0.113
540
BDY001 Body Dysmorphic Disorder 40 0.113
541
AGR018 Agraphia 37 0.113
542
OCL066 Oculogyric Crisis 34 0.113
543
P APL001 Aplastic Anemia 73 0.113
544
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.113
545
c HYP836 Hypercholesterolemia, Familial, 1 73 0.113
546
P HYP750 Hypertriglyceridemia, Familial 62 0.113
547
P DVL012 Developmental Dysplasia of the Hip 1 45 0.113
548
CHR630 Chorea, Benign Hereditary 42 0.113
549
P CLR023 Colorectal Cancer 100 0.113
550
P ANG001 Angelman Syndrome 65 0.113
551
RNL113 Renal Failure, Progressive, with Hypertension 31 0.113
552
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.113
553
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.113
554
PHL006 Phelan-Mcdermid Syndrome 62 0.113
555
P GLM040 Glioma Susceptibility 1 70 0.113
556
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.113
557
c THR092 Thrombophilia Due to Thrombin Defect 74 0.113
558
NRT004 Neuritis 53 0.113
559
P CHL002 Childhood Absence Epilepsy 63 0.113
560
DYS004 Dyscalculia 35 0.113
561
PYL006 Pyloric Stenosis 48 0.113
562
PHY002 Physical Disorder 41 0.113
563
P MYG005 Myoglobinuria 40 0.113
564
P PRG013 Paraganglioma 57 0.113
565
PRN009 Paranoid Schizophrenia 49 0.113
566
FTS001 Fetishism 28 0.113
567
P PLY019 Polyneuropathy 53 0.113
568
HYP007 Hypermobility Syndrome 35 0.113
569
P DRR001 Diarrhea 55 0.113
570
P TBR001 Tuberous Sclerosis 69 0.113
571
MLG169 Malignant Astrocytoma 57 0.113
572
LPD008 Lipid Metabolism Disorder 61 0.113
573
PRS021 Prostatic Adenoma 43 0.113
574
GRS001 Gerstmann Syndrome 41 0.113
575
ART017 Aortic Disease 49 0.113
576
CNN005 Connective Tissue Disease 66 0.113
577
SMT006 Somatoform Disorder 50 0.113
578
P PLC011 Pilocytic Astrocytoma 55 0.113
579
PLM031 Poliomyelitis 62 0.113
580
P MCR010 Microcephaly 59 0.113
581
PRS045 Prostatic Hypertrophy 52 0.113
582
ENT004 Enthesopathy 51 0.113
583
P VSC007 Vascular Disease 62 0.113
584
KLV001 Kluver-Bucy Syndrome 34 0.113
585
ACR007 Acromegaly 70 0.113
586
RTN020 Retinal Vascular Disease 45 0.113
587
HYP014 Hyperuricemia 51 0.113
588
P CRN025 Corneal Dystrophy 49 0.113
589
QDR001 Quadriplegia 49 0.113
590
P ECL001 Eclampsia 52 0.113
591
P HYP069 Hyperparathyroidism 62 0.113
592
BNG018 Benign Paroxysmal Positional Nystagmus 40 0.113
593
ACT038 Acute Retrobulbar Neuritis 24 0.113
594
GLS004 Glossopharyngeal Neuralgia 37 0.113
595
RTN021 Retinal Vascular Occlusion 45 0.113
596
VRT003 Vertebrobasilar Insufficiency 31 0.113
597
P OPT009 Optic Neuritis 57 0.113
598
P NTR004 Neutropenia 62 0.113
599
ATY001 Atypical Depressive Disorder 45 0.113
600
GST037 Gastroparesis 52 0.113
601
P PLY011 Polycystic Ovary Syndrome 57 0.113
602
GST033 Gestational Diabetes 61 0.113
603
P AGN002 Agnosia 53 0.113
604
OLF005 Olfactory Neuroblastoma 46 0.113
605
HYP066 Hyperglycemia 60 0.113
606
BLP006 Blepharoconjunctivitis 35 0.113
607
c CNT035 Central Nervous System Disease 53 0.113
608
BSM002 Bosma Arhinia Microphthalmia Syndrome 45 0.113
609
c PRK093 Parkinson Disease 8, Autosomal Dominant 49 0.113
610
ANR040 Aneurysm 60 0.113
611
CRB090 Cerebral Hypoxia 42 0.113
612
NRM005 Neuromuscular Disease 63 0.113
613
c PRM031 Primary Autosomal Recessive Microcephaly 55 0.113
614
c PRM212 Primary Microcephaly 40 0.113
615
HYP193 Hypocomplementemic Urticarial Vasculitis 32 0.113
616
SMN008 Semantic Dementia 47 0.113
617
SBP004 Subependymoma 39 0.113
618
OPD006 Opioid Addiction 48 0.113
619
THN005 Thunderclap Headache 15 0.113
620
TMP019 Temporomandibular Joint Anomaly 28 0.113
621
SHK001 Shaken Baby Syndrome 21 0.113
622
SPC005 Speech Disorder 46 0.113
623
P HMP007 Hemophilia 52 0.113
624
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 18 0.113
625
FSC004 Fasciitis 49 0.113
626
LNG099 Lung Disease 62 0.113
627
SCT002 Scotoma 42 0.113
628
P MYP004 Myopathy 67 0.113
629
P EYD002 Eye Disease 57 0.113
630
DYS003 Dysgraphia 35 0.113
631
IMP004 Impetigo 48 0.113
632
HYP264 Hypertonia 36 0.113
633
BRK012 Broken Heart Syndrome 42 0.113
634
BSL008 Basal Ganglia Disease 41 0.113
635
CNT015 Central Sleep Apnea 46 0.113
636
ILS001 Ileus 49 0.113
637
RFR003 Refractive Error 41 0.113
638
ALB002 Albinism 47 0.113
639
ASP037 Aspm Primary Microcephaly 10 0.113
641
IRR002 Irritable Bowel Syndrome 65 0.113
642
GRW007 Growth Hormone Deficiency 47 0.113
643
MDL007 Medial Medullary Syndrome 11 0.113
644
NCR007 Necrotizing Fasciitis 48 0.113
645
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 0.113
646
NRM001 Neuromyelitis Optica 60 0.113
647
c ACQ014 Acquired Hemophilia 45 0.113
648
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.113
649
PRG033 Progressive Non-Fluent Aphasia 52 0.113
650
ADG002 Audiogenic Seizures 25 0.113
651
SPC030 Specific Language Disorder 25 0.113
652
INH023 Inherited Cancer-Predisposing Syndrome 53 0.113
653
IDP092 Idiopathic/heritable Pulmonary Arterial Hypertension 43 0.113
654
RRS011 Rare Sleep Disorder 9 0.113
655
P PHC019 Pheochromocytoma-Paraganglioma 35 0.113
656
P OVR082 Overgrowth Syndrome 42 0.113
657
ACT181 Acute Motor Axonal Neuropathy 25 0.113
658
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.113
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