Search results for Methylphenidate

506 hits were found for Methylphenidate

# Family MCID Name MIFTS Score
1
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.393
2
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.550
3
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.458
4
CHL079 Children's Interstitial Lung Disease 26 0.247
5
P NRC002 Narcolepsy 52 0.242
6
BRN071 Brain Injury 49 0.235
7
DPR016 Depression 63 0.231
8
TRM010 Traumatic Brain Injury 51 0.231
9
P TCD001 Tic Disorder 53 0.225
10
ANX010 Anxiety 73 0.223
11
P SBS003 Substance Abuse 55 0.223
12
OPP004 Oppositional Defiant Disorder 49 0.217
13
ADL002 Adult Syndrome 70 0.192
14
CND002 Conduct Disorder 51 0.189
15
PSY004 Psychotic Disorder 67 0.187
16
MNT002 Mental Depression 58 0.180
17
P PRS038 Personality Disorder 65 0.175
18
CCN002 Cocaine Abuse 49 0.175
19
P ATS364 Autism 70 0.167
20
CCN001 Cocaine Dependence 48 0.167
21
DSS008 Disease of Mental Health 58 0.165
22
MDD011 Mood Disorder 62 0.154
23
P BPL003 Bipolar Disorder 56 0.154
24
c MJR024 Major Affective Disorder 9 41 0.154
25
c MJR022 Major Affective Disorder 8 38 0.154
26
P TRN020 Turner Syndrome 67 0.148
27
P DMN002 Dementia 66 0.148
28
P SLP005 Sleep Disorder 59 0.148
29
P PRV006 Pervasive Developmental Disorder 57 0.145
30
c ATS007 Autism Spectrum Disorder 67 0.142
31
P SZR006 Seizure Disorder 56 0.142
32
P PRK057 Parkinson Disease, Late-Onset 78 0.139
33
DWN001 Down Syndrome 70 0.135
34
P MJR001 Major Depressive Disorder 68 0.135
35
KHL003 Kohlschutter-Tonz Syndrome 65 0.135
36
P ALZ034 Alzheimer Disease 88 0.132
37
VSL002 Visual Epilepsy 59 0.132
38
ATX019 Ataxia with Vitamin E Deficiency 42 0.129
39
P EPL164 Epilepsy 71 0.118
40
RDN001 Reading Disorder 40 0.118
41
END040 Endogenous Depression 55 0.115
42
SBC016 Subacute Delirium 44 0.111
43
STR067 Stroke, Ischemic 81 0.107
44
OBS002 Obsessive-Compulsive Disorder 68 0.107
45
LRN003 Learning Disability 49 0.107
46
BRN028 Brain Cancer 74 0.102
47
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.102
48
P LKM062 Leukemia, Acute Lymphoblastic 69 0.102
49
ETN001 Eating Disorder 60 0.102
50
P TRM003 Tremor 54 0.102
51
NRT001 Neurotic Disorder 53 0.102
52
AVD001 Avoidant Personality Disorder 51 0.102
53
47X002 47,xyy 49 0.102
54
48X005 48,xyyy 39 0.102
55
CRD132 Cardiac Conduction Defect 58 0.098
56
OCL069 Ocular Motor Apraxia 51 0.098
57
DRG003 Drug Dependence 47 0.098
58
P MJR007 Major Affective Disorder 1 43 0.098
59
c MJR008 Major Affective Disorder 2 35 0.098
60
c MJR023 Major Affective Disorder 7 33 0.098
61
c MJR003 Major Affective Disorder 6 33 0.098
62
c MJR006 Major Affective Disorder 5 33 0.098
63
c MJR004 Major Affective Disorder 4 28 0.098
64
P SCH015 Schizophrenia 74 0.094
65
P MLT020 Multiple Sclerosis 72 0.094
66
ALC007 Alcohol Dependence 66 0.094
67
TBC004 Tobacco Addiction 64 0.094
68
CHR066 Chronic Fatigue Syndrome 61 0.094
69
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.094
70
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.094
71
DFC004 Deficiency Anemia 70 0.089
72
CRB039 Cerebrovascular Disease 67 0.089
73
c RHB024 Rhabdomyosarcoma 2 67 0.089
74
GLL008 Gilles De La Tourette Syndrome 66 0.089
75
P MVM001 Movement Disease 63 0.089
76
AGN016 Aging 56 0.089
77
BRD004 Borderline Personality Disorder 53 0.089
78
PRP007 Priapism 47 0.089
79
P DYS154 Dystonia 65 0.084
80
P ALC033 Alcohol Use Disorder 58 0.084
81
ANT011 Antisocial Personality Disorder 47 0.084
82
HDN002 Head Injury 46 0.084
83
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.078
84
ALL026 Allergic Hypersensitivity Disease 62 0.078
85
BLM002 Bulimia Nervosa 57 0.078
86
P HDC001 Headache 57 0.078
87
BKR002 Baker-Gordon Syndrome 49 0.078
88
TRP009 Triple X Syndrome 42 0.078
89
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.078
90
DVL001 Developmental Coordination Disorder 34 0.078
91
P PRS040 Prostate Cancer 97 0.072
92
c HYP595 Hypertension, Essential 84 0.072
93
SVR004 Severe Combined Immunodeficiency 73 0.072
94
P SRC025 Sarcoidosis 1 70 0.072
95
P LYM118 Lymphoma 68 0.072
96
P CRD119 Cardiac Arrest 67 0.072
97
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.072
98
PST028 Post-Traumatic Stress Disorder 58 0.072
99
CNT047 Contact Dermatitis 58 0.072
100
P EXN002 Exanthem 57 0.072
101
P NRF002 Neurofibromatosis 56 0.072
102
TRC010 Trichotillomania 51 0.072
103
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.072
104
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.072
105
P MYT002 Myotonic Dystrophy 49 0.072
106
SBS004 Substance Dependence 48 0.072
107
LYM019 Lymphosarcoma 46 0.072
108
PLY068 Polysubstance Abuse 43 0.072
109
GST020 Gastric Antral Vascular Ectasia 41 0.072
110
PSD088 Pseudobulbar Affect 36 0.072
111
CGN007 Cognitive Function 1, Social 27 0.072
112
DVL005 Developmental Dyspraxia 23 0.072
113
c NRF024 Neurofibromatosis, Type I 77 0.066
114
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.066
115
LPT014 Leptin Deficiency or Dysfunction 74 0.066
116
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.066
117
HMN044 Human Immunodeficiency Virus Type 1 71 0.066
118
P MYC007 Myocardial Infarction 70 0.066
119
P HYP086 Hypothyroidism 69 0.066
120
P NRV007 Nervous System Disease 66 0.066
121
CRN036 Craniopharyngioma 65 0.066
122
WLL001 Williams-Beuren Syndrome 60 0.066
123
ACQ007 Acquired Immunodeficiency Syndrome 60 0.066
124
PRT058 Pure Autonomic Failure 59 0.066
125
AMN003 Amnestic Disorder 54 0.066
126
STT041 Stuttering 52 0.066
127
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.066
128
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.066
129
BRX001 Bruxism 50 0.066
130
OPT003 Opiate Dependence 50 0.066
131
SCL003 Social Phobia 48 0.066
132
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.066
133
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.066
134
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.066
135
CNT033 Central Nervous System Cancer 47 0.066
136
RYN005 Raynaud Phenomenon 47 0.066
137
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.066
138
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.066
139
OPD001 Opioid Abuse 46 0.066
140
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.066
141
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.066
142
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.066
143
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.066
144
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.066
145
c PRS136 Prostate Cancer, Hereditary, 6 33 0.066
146
c PRS130 Prostate Cancer, Hereditary, 8 32 0.066
147
SDD004 Sudden Arrhythmia Death Syndrome 22 0.066
148
c ATT020 Attention Deficit-Hyperactivity Disorder 2 14 0.066
149
c ATR087 Atrial Standstill 1 75 0.059
150
CRB037 Cerebral Palsy 69 0.059
151
P LKM002 Leukemia 68 0.059
152
HYL004 Hyaline Fibromatosis Syndrome 67 0.059
153
P PLM037 Pulmonary Hypertension 67 0.059
154
MSM014 Mismatch Repair Cancer Syndrome 65 0.059
155
NRF007 Neurofibroma 64 0.059
156
P GLM045 Glioma 63 0.059
157
NTR005 Nutritional Deficiency Disease 62 0.059
158
LNG099 Lung Disease 60 0.059
159
ISC004 Ischemia 58 0.059
160
CNS004 Constipation 58 0.059
161
TRD006 Tardive Dyskinesia 54 0.059
162
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.059
163
VLC001 Velocardiofacial Syndrome 54 0.059
164
LYM040 Lymphoblastic Lymphoma 54 0.059
165
P PNC025 Panic Disorder 53 0.059
166
CHR073 Choreatic Disease 52 0.059
167
ACR041 Acromelic Frontonasal Dysostosis 52 0.059
168
LPT006 Leptin Receptor Deficiency 48 0.059
169
ACT084 Acute Stress Disorder 47 0.059
170
SRT004 Serotonin Syndrome 47 0.059
171
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.059
172
c MLG068 Malignant Glioma 46 0.059
173
GLL048 Glial Tumor 45 0.059
174
IMP006 Impulse Control Disorder 45 0.059
175
c SRC023 Sarcoidosis 2 43 0.059
176
CYT002 Cytokine Deficiency 42 0.059
177
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.059
178
ADS004 Aids Dementia Complex 40 0.059
179
HND015 Hand Skill, Relative 33 0.059
180
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.059
181
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.059
182
P LNG032 Lung Cancer 98 0.051
183
P GLM040 Glioma Susceptibility 1 81 0.051
184
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.051
185
IMM167 Immune Deficiency Disease 78 0.051
186
GLB015 Glioblastoma Multiforme 75 0.051
187
c MNN043 Meningioma, Familial 74 0.051
188
P FRG001 Fragile X Syndrome 70 0.051
189
P MLN008 Melanoma 69 0.051
190
c MYT021 Myotonic Dystrophy 1 69 0.051
191
SKN019 Skin Melanoma 68 0.051
192
FCT007 Factor Vii Deficiency 67 0.051
193
P OLG002 Oligodendroglioma 67 0.051
194
ANR007 Anorexia Nervosa 63 0.051
195
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.051
196
LPP008 Lipoprotein Quantitative Trait Locus 62 0.051
197
P VSC011 Vasculitis 62 0.051
198
MNN042 Meningioma, Radiation-Induced 62 0.051
199
c PNS012 Paine Syndrome 61 0.051
200
P ENC004 Encephalitis 61 0.051
201
P BNG030 Benign Ependymoma 60 0.051
202
INT066 Interstitial Lung Disease 60 0.051
203
STT001 Status Epilepticus 60 0.051
204
P OPT006 Optic Nerve Disease 60 0.051
205
GRD007 Grade Iii Astrocytoma 59 0.051
206
P PLY006 Polydactyly 59 0.051
207
c ACT075 Acute Myocardial Infarction 57 0.051
208
VSC002 Vascular Dementia 57 0.051
209
P NRP001 Neuropathy 56 0.051
210
ALL010 Allergic Contact Dermatitis 56 0.051
211
HYP005 Hypokalemia 55 0.051
212
P PLM034 Pulmonary Emphysema 55 0.051
213
JVN009 Juvenile Pilocytic Astrocytoma 55 0.051
214
GLS001 Gliosarcoma 54 0.051
215
P ALP008 Alopecia 54 0.051
216
CLL010 Cellular Ependymoma 54 0.051
217
SLP001 Sleeping Sickness 54 0.051
218
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.051
219
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.051
220
P BRN035 Brain Stem Glioma 52 0.051
221
P AST007 Astrocytoma 51 0.051
222
GNT002 Giant Cell Glioblastoma 50 0.051
223
SCH012 Schizoaffective Disorder 50 0.051
224
SPN021 Spinal Meningioma 50 0.051
225
P SCK005 Sickle Cell Disease 50 0.051
226
GYN001 Gynecomastia 49 0.051
227
GST049 Gastrointestinal System Cancer 49 0.051
228
PTH002 Pathological Gambling 49 0.051
229
CHL061 Childhood Leukemia 48 0.051
230
P ASP001 Asperger Syndrome 48 0.051
231
SXL003 Sexual Disorder 47 0.051
232
GST071 Gastrointestinal Carcinoma 47 0.051
233
ANP006 Anaplastic Ependymoma 46 0.051
234
OBS003 Obsessive-Compulsive Personality Disorder 46 0.051
235
CRN019 Coronary Artery Vasospasm 46 0.051
236
SBP004 Subependymoma 46 0.051
237
MYX001 Myxopapillary Ependymoma 46 0.051
238
SYN036 Syncope 45 0.051
239
MXD026 Mixed Glioma 45 0.051
240
AGR002 Agoraphobia 45 0.051
241
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.051
242
CYS009 Cystadenoma 44 0.051
243
CNN002 Cannabis Abuse 44 0.051
244
P EPN001 Ependymoblastoma 44 0.051
245
ANP009 Anaplastic Oligodendroglioma 43 0.051
246
c CHR056 Chronic Tic Disorder 43 0.051
247
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.051
248
c MLG064 Malignant Ependymoma 41 0.051
249
P HYP263 Hypersomnia 41 0.051
250
SCR001 Secretory Meningioma 41 0.051
251
P DYS005 Dyslexia 40 0.051
252
CNN001 Cannabis Dependence 40 0.051
253
AMP007 Amphetamine Abuse 37 0.051
254
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.051
255
MYT011 Myotonia 34 0.051
256
GST014 Gastrointestinal Lymphoma 34 0.051
257
c ADL008 Adult Oligodendroglioma 34 0.051
258
INF021 Infant Gynecomastia 31 0.051
259
c ADL054 Adult Brain Stem Glioma 30 0.051
260
PRR019 Perioral Myoclonia with Absences 27 0.051
261
CRB005 Cerebral Arteritis 26 0.051
262
c MLG023 Malignant Adult Ependymoma 15 0.051
263
c ADL045 Adult Ependymoblastoma 14 0.051
264
P BRS047 Breast Cancer 97 0.042
265
P PNC035 Pancreatic Cancer 84 0.042
266
NRL016 Neural Tube Defects 82 0.042
267
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.042
268
c DLT002 Dilated Cardiomyopathy 79 0.042
269
INS024 Insulin-Like Growth Factor I 79 0.042
270
MRF001 Marfan Syndrome 77 0.042
271
P HRT032 Heart Disease 75 0.042
272
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.042
273
SCK003 Sickle Cell Anemia 74 0.042
274
P OST002 Osteoporosis 74 0.042
275
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.042
276
P HNT016 Huntington Disease 72 0.042
277
P PHC003 Pheochromocytoma 71 0.042
278
P SLP006 Sleep Apnea 69 0.042
279
P CRN037 Craniosynostosis 68 0.042
280
P FRN006 Frontotemporal Dementia 68 0.042
281
P THR014 Thrombocytopenia 67 0.042
282
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.042
283
P LNG028 Long Qt Syndrome 66 0.042
284
c LNG044 Long Qt Syndrome 1 66 0.042
285
P HYD006 Hydrocephalus 66 0.042
286
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.042
287
DGR001 Digeorge Syndrome 64 0.042
288
P CRN300 Coronary Heart Disease 1 63 0.042
289
PNM010 Pneumothorax, Primary Spontaneous 60 0.042
290
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.042
291
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.042
292
P URT039 Urticaria 58 0.042
293
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.042
294
P CRD246 Cardiovascular System Disease 57 0.042
295
P FTL001 Fetal Alcohol Syndrome 57 0.042
296
PNM008 Pneumothorax 56 0.042
297
NRL004 Neuroleptic Malignant Syndrome 56 0.042
298
MRD002 Marden-Walker Syndrome 56 0.042
299
P DRR001 Diarrhea 55 0.042
300
HMP005 Hemiplegia 55 0.042
301
P NRM002 Normal Pressure Hydrocephalus 54 0.042
302
FCL014 Focal Epilepsy 54 0.042
303
PRC013 Pericarditis 54 0.042
304
CLL003 Cellulitis 54 0.042
305
HRT012 Heart Valve Disease 53 0.042
306
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.042
307
IMP005 Impotence 52 0.042
308
ART140 Arteries, Anomalies of 52 0.042
309
HYP781 Hypoascorbemia 51 0.042
310
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 49 0.042
311
c BPL002 Bipolar I Disorder 49 0.042
312
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.042
313
c BNG023 Benign Familial Infantile Epilepsy 48 0.042
314
OPD006 Opioid Addiction 48 0.042
315
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.042
316
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.042
317
ASP004 Asphyxia Neonatorum 46 0.042
318
ATN005 Autonomic Dysfunction 46 0.042
319
MTS001 Mutism 46 0.042
320
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.042
321
ADR040 Adrenal Gland Pheochromocytoma 46 0.042
322
P MYC033 Myoclonus 46 0.042
323
c DRR009 Diarrhea 6 46 0.042
324
CYN002 Cyanosis, Transient Neonatal 45 0.042
325
P CHR345 Chronic Pain 44 0.042
326
P BLP003 Blepharospasm 44 0.042
327
c ORT011 Orthostatic Hypotension 1 44 0.042
328
DMP001 Dumping Syndrome 44 0.042
329
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.042
330
NSP002 Nasopharyngitis 43 0.042
331
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.042
332
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.042
333
KLN009 Kleine-Levin Hibernation Syndrome 42 0.042
334
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.042
335
RST023 Resting Heart Rate, Variation in 41 0.042
336
49X006 49, Xxxxy Syndrome 41 0.042
337
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.042
338
c HMG001 Hemoglobin C Disease 40 0.042
339
SPR126 Superior Semicircular Canal Dehiscence 40 0.042
340
ALX001 Alexia 39 0.042
341
P FML340 Familial Episodic Pain Syndrome 39 0.042
342
c HMG029 Hemoglobin Se Disease 39 0.042
343
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.042
344
HYP835 Hypothalamic Obesity 38 0.042
345
KLP001 Kleptomania 38 0.042
346
c BLP048 Blepharospasm, Benign Essential 37 0.042
347
HRW001 Hair Whorl 36 0.042
349
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.042
350
SLF015 Self-Improving Collodion Baby 32 0.042
351
BRN049 Brain Tumor, Childhood 29 0.042
352
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.042
353
c ORT012 Orthostatic Hypotension 2 26 0.042
354
ORG003 Organic Mood Syndrome 14 0.042
356
P HPT023 Hepatocellular Carcinoma 100 0.030
357
P CLR023 Colorectal Cancer 99 0.030
358
ESP021 Esophageal Cancer 90 0.030
359
P GST053 Gastric Cancer 83 0.030
360
P BLD134 Bladder Cancer 79 0.030
361
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.030
362
P RSP003 Respiratory Failure 74 0.030
363
MSC157 Muscular Dystrophy, Duchenne Type 72 0.030
364
P KDN018 Kidney Disease 72 0.030
365
P NRB001 Neuroblastoma 72 0.030
366
P AMY004 Amyloidosis 70 0.030
367
CNG034 Congestive Heart Failure 69 0.030
368
ACR008 Acrocallosal Syndrome 69 0.030
369
CHL065 Cholangiocarcinoma 68 0.030
370
RCK004 Rickets 68 0.030
371
P HPT021 Hepatitis 67 0.030
372
ALL003 Allergic Rhinitis 67 0.030
373
P BLD062 Bile Duct Cancer 67 0.030
374
P MSC005 Muscular Dystrophy 66 0.030
375
HYP056 Hypoglycemia 66 0.030
376
c HRD010 Hereditary Spastic Paraplegia 66 0.030
377
c SML038 Small Cell Cancer of the Lung 65 0.030
378
SRC014 Sarcoma 65 0.030
379
P HRP006 Herpes Simplex 65 0.030
380
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.030
381
P DBT009 Diabetes Mellitus 64 0.030
382
ART002 Arts Syndrome 64 0.030
383
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.030
384
P ADN016 Adenocarcinoma 64 0.030
385
TRN015 Transient Cerebral Ischemia 63 0.030
386
c ATM011 Autoimmune Hepatitis 63 0.030
387
c FNC043 Fanconi Anemia, Complementation Group E 62 0.030
388
c BRN108 Branchiootic Syndrome 1 62 0.030
389
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.030
390
P ORT004 Orthostatic Intolerance 62 0.030
391
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 0.030
392
DRM006 Dermatitis 61 0.030
393
P ENC018 Encephalopathy 61 0.030
394
P STS008 Sotos Syndrome 1 61 0.030
395
P PNC044 Pancreatitis 61 0.030
396
VRL011 Viral Infectious Disease 61 0.030
397
APP008 Appendicitis 61 0.030
398
P SCL018 Scoliosis 60 0.030
399
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.030
400
RHM001 Rheumatic Fever 60 0.030
401
P CTR002 Cataract 60 0.030
402
P MYC008 Myocarditis 59 0.030
403
ADN018 Adenoma 59 0.030
404
ANR040 Aneurysm 59 0.030
405
P BCL017 B-Cell Lymphoma 58 0.030
406
P GLL018 Gallbladder Cancer 57 0.030
407
IRN002 Iron Metabolism Disease 57 0.030
408
P RHN004 Rhinitis 57 0.030
409
P PRN023 Prion Disease 57 0.030
410
c MST023 Mesothelioma, Malignant 57 0.030
411
APH002 Aphasia 57 0.030
412
P ANG015 Angioedema 57 0.030
413
c ESS001 Essential Tremor 56 0.030
414
SFT003 Soft Tissue Sarcoma 56 0.030
415
GNR004 Generalized Anxiety Disorder 56 0.030
416
ALL001 Allan-Herndon-Dudley Syndrome 56 0.030
417
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.030
418
HPT022 Hepatoblastoma 56 0.030
419
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.030
420
PRP030 Purpura 54 0.030
421
PTT009 Pituitary Gland Disease 54 0.030
422
P PTS002 Ptosis 53 0.030
423
SPN035 Spindle Cell Sarcoma 53 0.030
424
GST023 Gastric Ulcer 53 0.030
425
TXC002 Toxic Encephalopathy 53 0.030
426
DNT012 Dental Caries 53 0.030
427
PRP016 Paraplegia 52 0.030
428
HRP009 Herpes Simplex Encephalitis 52 0.030
429
P DDN001 Duodenal Ulcer 52 0.030
430
P RCT021 Rectum Cancer 52 0.030
431
PTH003 Pathologic Nystagmus 52 0.030
432
APR001 Apraxia 52 0.030
433
PNG002 Pain Agnosia 51 0.030
434
MYL020 Myelomeningocele 51 0.030
435
c VRL007 Viral Encephalitis 51 0.030
436
IRR003 Irritant Dermatitis 49 0.030
437
DYS009 Dysthymic Disorder 49 0.030
438
MNN009 Meningoencephalitis 49 0.030
439
WTH001 Withdrawal Disorder 48 0.030
440
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.030
441
TBR011 Tuberculous Meningitis 48 0.030
442
P TRT019 Torticollis 48 0.030
443
DLS001 Delusional Disorder 47 0.030
444
SPC010 Speech and Communication Disorders 47 0.030
445
KRT002 Keratomalacia 47 0.030
446
CRD137 Cardiogenic Shock 47 0.030
447
P PRC019 Precocious Puberty 46 0.030
448
c CNT075 Central Precocious Puberty 46 0.030
449
c ACT076 Acute Myocarditis 46 0.030
450
P BNG032 Benign Mesothelioma 46 0.030
451
CNV002 Conversion Disorder 45 0.030
452
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.030
453
NWC001 Newcastle Disease 45 0.030
454
OVR112 Ovarian Germ Cell Cancer 45 0.030
455
c CLR017 Clear Cell Sarcoma 45 0.030
456
SPS057 Spasticity 45 0.030
457
HPT067 Hepatocellular Adenoma 44 0.030
458
OVR063 Overnutrition 44 0.030
459
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.030
460
DPR002 Depersonalization Disorder 43 0.030
461
TST015 Testicular Disease 43 0.030
462
ENC005 Encephalomalacia 43 0.030
463
LWC001 Low Compliance Bladder 43 0.030
464
P CLS010 Cluster Headache 42 0.030
465
GLC096 Galactorrhea 42 0.030
466
PRS063 Paresthesia 41 0.030
467
PHB003 Phobia, Specific 41 0.030
468
PCD001 Pica Disease 41 0.030
469
NNT008 Neonatal Abstinence Syndrome 41 0.030
470
P MLG074 Malignant Mesenchymoma 40 0.030
471
KDN007 Kidney Clear Cell Sarcoma 40 0.030
472
ANX004 Anoxia 40 0.030
473
ART103 Arthrogryposis, Mental Retardation, and Seizures 40 0.030
474
ADJ001 Adjustment Disorder 40 0.030
475
UTR043 Uterine Sarcoma 39 0.030
476
ORM002 Oromandibular Dystonia 39 0.030
478
PHT008 Photosensitive Epilepsy 39 0.030
479
ANT019 Anterograde Amnesia 38 0.030
480
SPL006 Splenic Infarction 38 0.030
481
OVR094 Ovarian Epithelial Cancer 38 0.030
482
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.030
483
SPC031 Specific Learning Disability 37 0.030
484
PST086 Posterior Cortical Atrophy 37 0.030
485
FXD003 Fixed Drug Eruption 35 0.030
486
CYC001 Cycloplegia 35 0.030
487
GRM010 Germ Cells Tumors 34 0.030
489
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.030
490
AMN014 Aminopterin Syndrome Sine Aminopterin 33 0.030
491
PRD002 Periodic Limb Movement Disorder 33 0.030
492
CRN270 Coronary Artery Dissection, Spontaneous 32 0.030
493
IDP031 Idiopathic Hypersomnia 32 0.030
495
PST092 Posttransplant Acute Limbic Encephalitis 29 0.030
496
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.030
497
ACT162 Acute Sensory Ataxic Neuropathy 26 0.030
498
c JVN015 Juvenile Huntington Disease 26 0.030
499
MLG164 Malignant Epithelial Tumor of Ovary 26 0.030
500
PRT001 Partial Fetal Alcohol Syndrome 24 0.030
501
EXP001 Expressive Language Disorder 23 0.030
502
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 22 0.030
503
EXT039 Extrapontine Myelinolysis 18 0.030
504
APR010 Apraxia of Eyelid Opening 18 0.030
505
GRN059 Grn Frontotemporal Dementia 14 0.030
506
c ATT019 Attention Deficit-Hyperactivity Disorder 1 11 0.030
Content
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