Search results for Carbamazepine

746 hits were found for Carbamazepine

# Family MCID Name MIFTS Score
1
SVR097 Severe Cutaneous Adverse Reaction 69 4.932
2
CRB199 Carbamazepine Allergy 19 3.716
3
FTL049 Fetal Carbamazepine Syndrome 7 3.688
4
P SZR006 Seizure Disorder 56 0.427
5
VSL002 Visual Epilepsy 59 0.384
6
P EPL164 Epilepsy 71 0.365
7
ALL026 Allergic Hypersensitivity Disease 62 0.312
8
P BPL003 Bipolar Disorder 56 0.305
9
c MJR024 Major Affective Disorder 9 41 0.303
10
c MJR022 Major Affective Disorder 8 38 0.303
11
TRG002 Trigeminal Neuralgia 60 0.301
12
ERY003 Erythema Multiforme 58 0.297
13
P EXN002 Exanthem 57 0.297
14
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.287
15
ERY066 Erythema Multiforme Major 30 0.283
16
FCL014 Focal Epilepsy 54 0.271
17
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.261
18
P HYP098 Hypereosinophilic Syndrome 67 0.214
19
OCL069 Ocular Motor Apraxia 51 0.196
20
P MJR007 Major Affective Disorder 1 43 0.178
21
P TMP001 Temporal Lobe Epilepsy 50 0.158
22
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.158
23
MDD011 Mood Disorder 62 0.154
24
STT001 Status Epilepticus 60 0.154
25
c BPL002 Bipolar I Disorder 49 0.151
26
WTH001 Withdrawal Disorder 48 0.149
27
P DBT005 Diabetes Insipidus 55 0.147
28
P THR014 Thrombocytopenia 67 0.145
29
P NTR004 Neutropenia 63 0.142
30
SCH012 Schizoaffective Disorder 50 0.135
31
P MYC033 Myoclonus 46 0.135
32
DPR016 Depression 63 0.132
33
P NRP001 Neuropathy 56 0.132
34
PTH003 Pathologic Nystagmus 52 0.132
35
GRN017 Granulocytopenia 44 0.132
36
P LPS004 Lupus Erythematosus 61 0.125
37
P TRM003 Tremor 54 0.125
38
P SCH015 Schizophrenia 74 0.122
39
MNT002 Mental Depression 58 0.119
40
P DYS154 Dystonia 65 0.113
41
c SYS001 Systemic Lupus Erythematosus 86 0.110
42
NRL016 Neural Tube Defects 82 0.110
43
ATR057 Atrioventricular Block 55 0.110
44
CCN001 Cocaine Dependence 48 0.110
45
c MJR008 Major Affective Disorder 2 35 0.110
46
c MJR023 Major Affective Disorder 7 33 0.110
47
c MJR003 Major Affective Disorder 6 33 0.110
48
c MJR006 Major Affective Disorder 5 33 0.110
49
c MJR004 Major Affective Disorder 4 28 0.110
50
P HPT021 Hepatitis 67 0.107
51
P ENC018 Encephalopathy 61 0.107
52
P PRS038 Personality Disorder 65 0.104
53
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.101
54
P CHR345 Chronic Pain 44 0.101
55
EXF003 Exfoliative Dermatitis 27 0.101
56
P HYP086 Hypothyroidism 69 0.097
57
c MGR028 Migraine with or Without Aura 1 67 0.097
58
DRM006 Dermatitis 61 0.097
59
NRL004 Neuroleptic Malignant Syndrome 56 0.097
60
END040 Endogenous Depression 55 0.097
61
P KDN018 Kidney Disease 72 0.094
62
P PRP029 Porphyria 62 0.094
63
P PRP019 Peripheral Nervous System Disease 58 0.094
64
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.094
65
DBT010 Diabetic Neuropathy 54 0.094
66
SYN036 Syncope 45 0.094
67
SBC016 Subacute Delirium 44 0.094
68
ADL002 Adult Syndrome 70 0.090
69
c ACT071 Acute Kidney Failure 60 0.090
70
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 0.090
71
P DRR001 Diarrhea 55 0.090
72
P TCD001 Tic Disorder 53 0.090
73
GLS004 Glossopharyngeal Neuralgia 34 0.090
74
P DMN002 Dementia 66 0.086
75
48X005 48,xyyy 39 0.086
76
P APL001 Aplastic Anemia 74 0.082
77
P LYM118 Lymphoma 68 0.082
78
PSY004 Psychotic Disorder 67 0.082
79
ALC007 Alcohol Dependence 66 0.082
80
P PNC025 Panic Disorder 53 0.082
81
CHR073 Choreatic Disease 52 0.082
83
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.082
84
HDN002 Head Injury 46 0.082
85
P RSP003 Respiratory Failure 74 0.078
86
P DBT009 Diabetes Mellitus 64 0.078
87
P MVM001 Movement Disease 63 0.078
88
P SBS003 Substance Abuse 55 0.078
89
BRD004 Borderline Personality Disorder 53 0.078
90
P FBR031 Febrile Seizures 53 0.078
91
OST011 Osteomalacia 52 0.078
92
TRM010 Traumatic Brain Injury 51 0.078
93
CCN002 Cocaine Abuse 49 0.078
94
BRN071 Brain Injury 49 0.078
95
CNT106 Centralopathic Epilepsy 35 0.078
96
GRN009 Granulomatous Hepatitis 33 0.078
97
P PNM007 Pneumonia 68 0.073
98
P MJR001 Major Depressive Disorder 68 0.073
99
P EPL140 Epilepsy, Idiopathic Generalized 62 0.073
100
CHL068 Cholestasis 61 0.073
101
P ALC033 Alcohol Use Disorder 58 0.073
102
MYT011 Myotonia 34 0.073
103
AST005 Asthma 76 0.069
104
ANX010 Anxiety 73 0.069
105
P NRB001 Neuroblastoma 72 0.069
106
DWN001 Down Syndrome 70 0.069
107
CNG034 Congestive Heart Failure 69 0.069
108
CRB037 Cerebral Palsy 69 0.069
109
P LVR013 Liver Disease 68 0.069
110
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.069
111
P AGM001 Agammaglobulinemia 65 0.069
112
KRN002 Kearns-Sayre Syndrome 63 0.069
113
CLT003 Colitis 62 0.069
114
TRD006 Tardive Dyskinesia 54 0.069
115
47X002 47,xyy 49 0.069
116
INT067 Interstitial Nephritis 48 0.069
117
P PRR002 Pure Red-Cell Aplasia 47 0.069
118
P ERY008 Erythromelalgia 47 0.069
119
RDC006 Red Cell Aplasia 43 0.069
120
DRG024 Drug Allergy 42 0.069
121
CMP006 Complex Partial Epilepsy 36 0.069
122
MYC006 Mycosis Fungoides 66 0.064
123
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.064
124
PRP083 Porphyria, Acute Intermittent 64 0.064
125
P VSC011 Vasculitis 62 0.064
126
HRP004 Herpes Zoster 60 0.064
127
BRN002 Bronchiolitis 59 0.064
128
c ACT134 Acute Liver Failure 56 0.064
129
BRN012 Bronchiolitis Obliterans 55 0.064
130
P ALP008 Alopecia 54 0.064
131
HMC014 Homocysteinemia 53 0.064
132
P CHL066 Cholangitis 51 0.064
133
BNR002 Bone Resorption Disease 48 0.064
134
P HMF004 Hemifacial Spasm 38 0.064
135
c HMF011 Hemifacial Spasm, Familial 33 0.064
136
SPC030 Specific Language Disorder 26 0.064
137
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.058
138
STR067 Stroke, Ischemic 81 0.058
139
P MLT020 Multiple Sclerosis 72 0.058
140
HMN044 Human Immunodeficiency Virus Type 1 71 0.058
141
DFC004 Deficiency Anemia 70 0.058
142
OBS002 Obsessive-Compulsive Disorder 68 0.058
143
RCK004 Rickets 68 0.058
144
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.058
145
P MNN013 Meningitis 66 0.058
146
TTN003 Tetanus 65 0.058
147
CLF027 Cleft Palate, Isolated 64 0.058
148
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.058
149
SKN016 Skin Disease 63 0.058
150
ERL001 Early Myoclonic Encephalopathy 62 0.058
151
P PNC044 Pancreatitis 61 0.058
152
P BND020 Bone Disease 59 0.058
153
P URT039 Urticaria 58 0.058
154
P HDC001 Headache 57 0.058
155
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.058
156
P MYT023 Myotonia Congenita 56 0.058
157
P SCK002 Sick Sinus Syndrome 55 0.058
158
P RST001 Restless Legs Syndrome 54 0.058
159
NRT001 Neurotic Disorder 53 0.058
160
TXC002 Toxic Encephalopathy 53 0.058
161
PNG002 Pain Agnosia 51 0.058
162
ILS001 Ileus 51 0.058
163
ASP003 Aseptic Meningitis 51 0.058
164
c ACT078 Acute Porphyria 51 0.058
165
P OVR082 Overgrowth Syndrome 50 0.058
166
SYD002 Sydenham Chorea 44 0.058
167
KLN009 Kleine-Levin Hibernation Syndrome 42 0.058
168
LYM042 Lymphocytic Colitis 41 0.058
169
INT025 Intermittent Explosive Disorder 41 0.058
170
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.058
171
PFF001 Pfeiffer Syndrome 79 0.052
172
IMM167 Immune Deficiency Disease 78 0.052
173
P HRT032 Heart Disease 75 0.052
174
SVR004 Severe Combined Immunodeficiency 73 0.052
175
P VSC007 Vascular Disease 63 0.052
176
P PSR002 Psoriasis 62 0.052
177
LVR012 Liver Cirrhosis 62 0.052
178
HYP066 Hyperglycemia 61 0.052
179
c PNS012 Paine Syndrome 61 0.052
180
P MYC008 Myocarditis 59 0.052
181
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.052
182
SBC001 Subacute Sclerosing Panencephalitis 56 0.052
183
P PLY019 Polyneuropathy 56 0.052
184
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.052
185
HYP060 Hyperinsulinism 54 0.052
186
PRP030 Purpura 54 0.052
187
P EPS030 Episodic Kinesigenic Dyskinesia 1 54 0.052
188
PLM010 Pulmonary Edema 54 0.052
189
PNC001 Pancytopenia 54 0.052
190
PST011 Pustulosis of Palm and Sole 52 0.052
191
P ESN008 Eosinophilic Pneumonia 50 0.052
192
OPT003 Opiate Dependence 50 0.052
193
SNT005 Sinoatrial Node Disease 49 0.052
194
QDR001 Quadriplegia 48 0.052
195
SXL003 Sexual Disorder 47 0.052
196
P BLP003 Blepharospasm 44 0.052
197
ATX019 Ataxia with Vitamin E Deficiency 42 0.052
198
PRS063 Paresthesia 41 0.052
199
PST053 Postherpetic Neuralgia 40 0.052
200
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 0.052
201
OCL066 Oculogyric Crisis 38 0.052
202
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.052
203
c ACT036 Acute Cholangitis 36 0.052
204
PSD088 Pseudobulbar Affect 36 0.052
205
CHL079 Children's Interstitial Lung Disease 26 0.052
206
ANT078 Antipyrine Metabolism 24 0.052
207
P ALZ034 Alzheimer Disease 88 0.045
208
P CNR004 Cone-Rod Dystrophy 2 73 0.045
209
c HPT073 Hepatitis C Virus 72 0.045
210
P ATS364 Autism 70 0.045
211
P TBR001 Tuberous Sclerosis 70 0.045
212
P MYS003 Myasthenia Gravis 68 0.045
213
CRB039 Cerebrovascular Disease 67 0.045
214
CRP001 Carpal Tunnel Syndrome 67 0.045
215
KHL003 Kohlschutter-Tonz Syndrome 65 0.045
216
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.045
217
PRT037 Pertussis 65 0.045
218
P GLM045 Glioma 63 0.045
219
c HPT001 Hepatitis C 62 0.045
220
WST001 West Syndrome 61 0.045
221
P ENC004 Encephalitis 61 0.045
222
SPN186 Spinal Cord Injury 60 0.045
223
c ACT027 Acute Pancreatitis 60 0.045
224
RHM001 Rheumatic Fever 60 0.045
225
P SLP005 Sleep Disorder 59 0.045
226
P GLL022 Guillain-Barre Syndrome 59 0.045
227
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.045
228
PST028 Post-Traumatic Stress Disorder 58 0.045
229
CMP010 Complex Regional Pain Syndrome 58 0.045
230
LNN001 Lennox-Gastaut Syndrome 57 0.045
231
P ANG015 Angioedema 57 0.045
232
P PLY011 Polycystic Ovary Syndrome 56 0.045
233
P PMP001 Pemphigus 54 0.045
234
SNS003 Sensory Peripheral Neuropathy 54 0.045
235
STT041 Stuttering 52 0.045
236
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.045
237
c VRL010 Viral Hepatitis 52 0.045
238
IMP005 Impotence 52 0.045
239
CND002 Conduct Disorder 51 0.045
240
P AST007 Astrocytoma 51 0.045
241
P HYP040 Hypospadias 51 0.045
242
SMT006 Somatoform Disorder 50 0.045
243
DYS073 Dysphagia 50 0.045
244
HRT011 Heart Septal Defect 50 0.045
245
SCH068 Schwartz-Jampel Syndrome, Type 1 49 0.045
246
SBS004 Substance Dependence 48 0.045
247
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.045
248
PLM035 Pulmonary Eosinophilia 48 0.045
249
DRG013 Drug-Induced Lupus Erythematosus 48 0.045
250
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.045
251
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.045
252
GLL048 Glial Tumor 45 0.045
253
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.045
254
NSP002 Nasopharyngitis 43 0.045
255
P HYP265 Hypotonia 43 0.045
256
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.045
257
49X006 49, Xxxxy Syndrome 41 0.045
258
MLN003 Melancholia 38 0.045
259
FXD003 Fixed Drug Eruption 35 0.045
260
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.045
261
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.045
262
PPL052 Papillomatosis, Confluent and Reticulated 33 0.045
263
CYT018 Cytochrome P450 2d6 Variant 27 0.045
264
ADG002 Audiogenic Seizures 25 0.045
265
PRX022 Paroxysmal Choreoathetosis 24 0.045
266
DPS001 Dipsogenic Diabetes Insipidus 23 0.045
267
CTN031 Cutaneous Pseudolymphoma 18 0.045
268
TRG017 Trigeminal Trophic Syndrome 17 0.045
269
SCN086 Scn9a Neuropathic Pain Syndromes 9 0.045
270
P CLR023 Colorectal Cancer 99 0.037
271
BRN028 Brain Cancer 74 0.037
272
P OST002 Osteoporosis 74 0.037
273
c MNN043 Meningioma, Familial 74 0.037
274
c THR092 Thrombophilia Due to Thrombin Defect 73 0.037
275
P HNT016 Huntington Disease 72 0.037
276
P MYC007 Myocardial Infarction 70 0.037
277
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.037
278
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.037
279
GST092 Gastroesophageal Reflux 67 0.037
280
c ATS007 Autism Spectrum Disorder 67 0.037
281
P PLM037 Pulmonary Hypertension 67 0.037
282
c RHB024 Rhabdomyosarcoma 2 67 0.037
283
HYP056 Hypoglycemia 66 0.037
284
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.037
285
P HRP006 Herpes Simplex 65 0.037
286
ATH013 Atherosclerosis Susceptibility 65 0.037
287
GT001 Gout 64 0.037
288
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.037
289
P HML002 Hemolytic Anemia 63 0.037
290
P HYP069 Hyperparathyroidism 63 0.037
291
c BRN108 Branchiootic Syndrome 1 62 0.037
292
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.037
293
MNN042 Meningioma, Radiation-Induced 62 0.037
294
TXC005 Toxic Shock Syndrome 62 0.037
295
P SCL018 Scoliosis 60 0.037
296
P VNT002 Ventricular Septal Defect 60 0.037
297
CRD223 Cardiac Arrhythmia 60 0.037
298
ACQ007 Acquired Immunodeficiency Syndrome 60 0.037
299
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.037
300
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.037
301
CHL014 Cholera 59 0.037
302
PLM033 Pulmonary Embolism 59 0.037
303
GST045 Gastroenteritis 59 0.037
304
PPT005 Peptic Ulcer Disease 59 0.037
305
P ANP001 Anaplastic Large Cell Lymphoma 58 0.037
306
ISC004 Ischemia 58 0.037
307
PRX015 Paroxysmal Extreme Pain Disorder 58 0.037
308
CNT047 Contact Dermatitis 58 0.037
309
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.037
310
LYM027 Lymphopenia 58 0.037
311
P GLM007 Glomerulonephritis 57 0.037
312
MCR013 Microphthalmia 57 0.037
313
THR024 Thrombosis 57 0.037
314
CMR002 Coumarin Resistance 56 0.037
315
AGN016 Aging 56 0.037
316
P GST044 Gastritis 56 0.037
317
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.037
318
AMN003 Amnestic Disorder 54 0.037
319
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.037
320
P LCH002 Lichen Planus 53 0.037
321
CRY001 Cryptogenic Organizing Pneumonia 53 0.037
322
P FML023 Familial Hemiplegic Migraine 53 0.037
323
P CTN003 Cutaneous Lupus Erythematosus 53 0.037
324
CLF001 Cleft Lip 53 0.037
325
CLB010 Coloboma of Macula 52 0.037
326
ACR041 Acromelic Frontonasal Dysostosis 52 0.037
327
MYL020 Myelomeningocele 51 0.037
328
GNG012 Gingival Overgrowth 51 0.037
329
BHR001 Behr Syndrome 51 0.037
330
c HNT004 Huntington Disease-Like 2 50 0.037
331
SPN021 Spinal Meningioma 50 0.037
332
PRN009 Paranoid Schizophrenia 50 0.037
333
c BNG006 Benign Familial Neonatal Epilepsy 50 0.037
334
PTH002 Pathological Gambling 49 0.037
335
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.037
336
SPL018 Splenomegaly 48 0.037
337
ACT084 Acute Stress Disorder 47 0.037
338
P CLL015 Collagen Disease 47 0.037
339
SRT004 Serotonin Syndrome 47 0.037
340
SMT001 Somatization Disorder 46 0.037
341
HPT004 Hepatic Coma 45 0.037
342
IMM003 Immunoglobulin Alpha Deficiency 45 0.037
343
SPS057 Spasticity 45 0.037
344
DRG002 Drug-Induced Hepatitis 43 0.037
345
CYT002 Cytokine Deficiency 42 0.037
346
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.037
347
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.037
348
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.037
349
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.037
350
P PHT010 Photoparoxysmal Response 1 42 0.037
351
SCR001 Secretory Meningioma 41 0.037
352
RFL002 Reflex Epilepsy 40 0.037
353
SPS004 Spastic Quadriplegia 39 0.037
354
DSS010 Dissociative Disorder 39 0.037
355
PHT008 Photosensitive Epilepsy 39 0.037
356
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.037
357
c HNT011 Huntington Disease-Like 3 38 0.037
358
SCR039 Scorpion Envenomation 38 0.037
359
HRW001 Hair Whorl 36 0.037
360
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.037
361
KLV001 Kluver-Bucy Syndrome 34 0.037
362
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.037
363
PRX097 Paroxysmal Dystonia 32 0.037
364
c MLT010 Multiple Personality Disorder 30 0.037
365
PRS120 Persistent Idiopathic Facial Pain 28 0.037
366
FCL007 Facial Neuralgia 27 0.037
367
CRN309 Cranial Neuralgia 22 0.037
368
P HPT023 Hepatocellular Carcinoma 100 0.026
369
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.026
370
MYL069 Myeloma, Multiple 85 0.026
371
c LKM061 Leukemia, Acute Myeloid 84 0.026
372
c HYP595 Hypertension, Essential 84 0.026
373
P GLM040 Glioma Susceptibility 1 81 0.026
374
P LKM071 Leukemia, Chronic Lymphocytic 79 0.026
375
INS024 Insulin-Like Growth Factor I 79 0.026
376
c TBR025 Tuberous Sclerosis 1 77 0.026
377
GLB015 Glioblastoma Multiforme 75 0.026
378
c HYP836 Hypercholesterolemia, Familial, 1 73 0.026
379
c SPN225 Spondyloarthropathy 1 73 0.026
380
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.026
381
c TBR026 Tuberous Sclerosis 2 72 0.026
382
P GRF003 Graft-Versus-Host Disease 72 0.026
383
c LKM063 Leukemia, Chronic Myeloid 72 0.026
384
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.026
385
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.026
386
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.026
387
P MYP004 Myopathy 70 0.026
388
CRT072 Creutzfeldt-Jakob Disease 70 0.026
389
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.026
390
P SLP006 Sleep Apnea 69 0.026
391
LYM133 Lymphoma, Hodgkin, Classic 69 0.026
392
P TMP003 Temporal Arteritis 68 0.026
393
P LKM002 Leukemia 68 0.026
394
P INF038 Influenza 68 0.026
395
CNN005 Connective Tissue Disease 68 0.026
396
P FRN006 Frontotemporal Dementia 68 0.026
397
FCT007 Factor Vii Deficiency 67 0.026
398
P OLG002 Oligodendroglioma 67 0.026
399
P FLL037 Follicular Lymphoma 67 0.026
400
ALL003 Allergic Rhinitis 67 0.026
401
P PRP003 Porphyria Cutanea Tarda 67 0.026
402
P MCR115 Microvascular Complications of Diabetes 5 66 0.026
403
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.026
404
P ATR011 Atrial Fibrillation 66 0.026
405
CHG001 Chagas Disease 66 0.026
406
P HYD006 Hydrocephalus 66 0.026
407
P DRM053 Dermatitis, Atopic 66 0.026
408
P ART005 Arteriovenous Malformation 65 0.026
409
P CNJ013 Conjunctivitis 65 0.026
410
KWS002 Kawasaki Disease 65 0.026
411
P ADL010 Adult Respiratory Distress Syndrome 65 0.026
412
CLN015 Colon Adenocarcinoma 65 0.026
413
P CHR071 Charcot-Marie-Tooth Disease 65 0.026
414
MSC007 Muscle Hypertrophy 64 0.026
415
PLM031 Poliomyelitis 64 0.026
416
P ADN016 Adenocarcinoma 64 0.026
417
LYM017 Lyme Disease 64 0.026
418
HYP020 Hyperprolactinemia 64 0.026
419
P ERL057 Early Infantile Epileptic Encephalopathy 63 0.026
420
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.026
421
P CRN300 Coronary Heart Disease 1 63 0.026
422
HYP780 Hypoadrenocorticism, Familial 63 0.026
423
HLT001 Holt-Oram Syndrome 63 0.026
424
c ACT068 Acute Cystitis 63 0.026
425
TRN015 Transient Cerebral Ischemia 63 0.026
426
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.026
427
c FNC043 Fanconi Anemia, Complementation Group E 62 0.026
428
c HPT003 Hepatitis a 62 0.026
429
P TRC086 Trichohepatoenteric Syndrome 1 62 0.026
430
BLL006 Bullous Pemphigoid 62 0.026
431
LSC001 Lesch-Nyhan Syndrome 62 0.026
432
ATM095 Autoimmune Disease 62 0.026
433
P PRM006 Primary Biliary Cirrhosis 62 0.026
434
MSL001 Measles 62 0.026
435
FTT001 Fatty Liver Disease 61 0.026
436
P CHL002 Childhood Absence Epilepsy 61 0.026
437
VRL011 Viral Infectious Disease 61 0.026
438
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.026
439
P MYL006 Myeloid Leukemia 60 0.026
440
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.026
441
P TXP001 Toxoplasmosis 60 0.026
442
HPT019 Hepatic Encephalopathy 60 0.026
443
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.026
444
c EPS042 Episodic Ataxia, Type 1 60 0.026
445
LNG099 Lung Disease 60 0.026
446
P ATR010 Atrial Heart Septal Defect 60 0.026
447
P SNS001 Sensorineural Hearing Loss 60 0.026
448
VRC005 Varicose Veins 60 0.026
449
NLP001 Nail-Patella Syndrome 60 0.026
450
P OPT006 Optic Nerve Disease 60 0.026
451
P MCR010 Microcephaly 59 0.026
452
c HPT016 Hepatitis B 59 0.026
453
P PRD006 Prader-Willi Syndrome 59 0.026
454
P LYM033 Lymphoproliferative Syndrome 59 0.026
455
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.026
456
GRD007 Grade Iii Astrocytoma 59 0.026
457
ADN018 Adenoma 59 0.026
458
CRY005 Cryptococcosis 58 0.026
459
P BCL017 B-Cell Lymphoma 58 0.026
460
FBR047 Fibromyalgia 58 0.026
461
c PRM005 Primary Hyperparathyroidism 58 0.026
462
CCC001 Coccidioidomycosis 58 0.026
463
BRS051 Breast Disease 58 0.026
464
EYD002 Eye Disease 58 0.026
465
DSS008 Disease of Mental Health 58 0.026
466
P MMP001 Mumps 58 0.026
467
CNS004 Constipation 58 0.026
468
P CND004 Candidiasis 58 0.026
469
EXT034 Extrinsic Allergic Alveolitis 58 0.026
470
P INF032 Infertility 57 0.026
471
P UVT001 Uveitis 57 0.026
472
PMP006 Pemphigus Vulgaris, Familial 57 0.026
473
c CHL119 Cholangitis, Primary Sclerosing 57 0.026
474
P MYM013 Moyamoya Disease 1 57 0.026
475
CHR105 Choreoacanthocytosis 57 0.026
476
P FTL001 Fetal Alcohol Syndrome 57 0.026
477
BLR008 Bilirubin Metabolic Disorder 57 0.026
478
VSC002 Vascular Dementia 57 0.026
479
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.026
480
HYP266 Hypoxia 57 0.026
481
P MYS005 Myositis 56 0.026
482
EXF001 Exfoliation Syndrome 56 0.026
483
c ESS001 Essential Tremor 56 0.026
484
GNR004 Generalized Anxiety Disorder 56 0.026
485
SCH003 Schizophreniform Disorder 56 0.026
486
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.026
487
VRG001 Variegate Porphyria 56 0.026
488
ANN002 Anencephaly 56 0.026
489
SML019 Smallpox 56 0.026
490
c GRV008 Graves Disease 1 56 0.026
491
P AGN002 Agnosia 55 0.026
492
HYP005 Hypokalemia 55 0.026
493
P ATR001 Atrioventricular Septal Defect 55 0.026
494
MMB001 Membranoproliferative Glomerulonephritis 55 0.026
495
P MLN007 Male Infertility 55 0.026
496
P ANT006 Antiphospholipid Syndrome 55 0.026
497
P MYP006 Myopia 55 0.026
498
P PTT006 Pituitary Adenoma 55 0.026
499
P HYP076 Hyperthyroidism 55 0.026
500
HMP005 Hemiplegia 55 0.026
501
CLF004 Cleft Lip/palate 54 0.026
502
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.026
503
GLS001 Gliosarcoma 54 0.026
504
RFL001 Reflex Sympathetic Dystrophy 54 0.026
505
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.026
506
PRT038 Protein-Energy Malnutrition 54 0.026
507
BRN014 Bronchopneumonia 54 0.026
508
THR013 Thoracic Outlet Syndrome 54 0.026
509
PRC013 Pericarditis 54 0.026
510
P LTR001 Lateral Sclerosis 54 0.026
511
NNL006 Non-Alcoholic Steatohepatitis 54 0.026
512
P BRC006 Brachydactyly 53 0.026
513
KRT006 Keratoconjunctivitis 53 0.026
514
CYS005 Cysticercosis 53 0.026
515
FNG017 Fungal Infectious Disease 53 0.026
516
P ALT001 Alternating Hemiplegia of Childhood 53 0.026
517
GTR002 Goiter 53 0.026
518
P PTS002 Ptosis 53 0.026
519
IRD001 Iridocyclitis 53 0.026
520
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.026
521
P ATN002 Autonomic Nervous System Disease 52 0.026
522
FRY006 Fryns Microphthalmia Syndrome 52 0.026
523
EXP004 Exophthalmos 52 0.026
524
DMY004 Demyelinating Disease 52 0.026
525
HRP009 Herpes Simplex Encephalitis 52 0.026
526
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.026
527
P NRC002 Narcolepsy 52 0.026
528
HYP014 Hyperuricemia 52 0.026
529
APR001 Apraxia 52 0.026
530
SPN051 Spondylitis 51 0.026
531
OLG003 Oligohydramnios 51 0.026
532
AVD001 Avoidant Personality Disorder 51 0.026
533
MYL001 Myelitis 51 0.026
534
PLS009 Plasma Cell Neoplasm 51 0.026
535
P LCT001 Lactic Acidosis 51 0.026
536
NRM004 Neuroma 51 0.026
537
P PRC012 Pericardial Effusion 51 0.026
538
c SCN007 Secondary Hyperparathyroidism 51 0.026
539
GNT002 Giant Cell Glioblastoma 50 0.026
540
P MMB011 Membranous Nephropathy 50 0.026
541
BRN009 Burning Mouth Syndrome 50 0.026
542
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.026
543
FSC004 Fasciitis 50 0.026
544
STM007 Stomatitis 50 0.026
545
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.026
546
MTB004 Metabolic Acidosis 50 0.026
547
BLR001 Biliary Atresia 50 0.026
548
HYP748 Hypertelorism 50 0.026
549
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.026
550
HYP080 Hypogonadism 50 0.026
551
DBT004 Diabetic Polyneuropathy 49 0.026
552
P BNG026 Benign Neonatal Seizures 49 0.026
553
ENT004 Enthesopathy 49 0.026
554
LFT001 Left Bundle Branch Hemiblock 49 0.026
555
HDR003 Hidradenitis 49 0.026
556
SPT005 Spotted Fever 49 0.026
557
MNN009 Meningoencephalitis 49 0.026
558
CHR222 Chromosome 1p36 Deletion Syndrome 49 0.026
559
ACT029 Acute Interstitial Pneumonia 49 0.026
560
URM002 Uremia 49 0.026
561
P CTN015 Cutaneous T Cell Lymphoma 49 0.026
562
HST010 Histiocytosis 48 0.026
563
RYN001 Raynaud Disease 48 0.026
564
HYP043 Hyperandrogenism 48 0.026
565
ATS010 Autosomal Recessive Disease 48 0.026
566
ADT003 Auditory System Disease 48 0.026
567
ASP007 Aspiration Pneumonia 48 0.026
568
P CLR019 Color Blindness 48 0.026
569
P SCL009 Sclerosing Cholangitis 48 0.026
570
RGH001 Right Bundle Branch Block 48 0.026
571
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.026
572
P SCL015 Scleritis 48 0.026
573
HMP001 Hemopericardium 48 0.026
574
CHL056 Cheilitis 48 0.026
575
P MRC003 Mercury Poisoning 48 0.026
576
PRP007 Priapism 47 0.026
577
DRY001 Dry Eye Syndrome 47 0.026
578
CRD001 Cardiac Tamponade 47 0.026
579
SPC010 Speech and Communication Disorders 47 0.026
580
CNT033 Central Nervous System Cancer 47 0.026
581
CRD137 Cardiogenic Shock 47 0.026
582
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.026
583
RYN005 Raynaud Phenomenon 47 0.026
584
ATN005 Autonomic Dysfunction 46 0.026
585
P LPM005 Lipomatosis 46 0.026
586
TTH006 Tooth Disease 46 0.026
587
EXS001 Exostosis 46 0.026
588
PLL012 Pollen Allergy 46 0.026
589
P BRB001 Beriberi 46 0.026
590
FLL008 Folliculitis 46 0.026
591
OBS003 Obsessive-Compulsive Personality Disorder 46 0.026
592
P HMR005 Hemorrhoid 46 0.026
593
OBS004 Obstructive Hydrocephalus 46 0.026
594
OPD001 Opioid Abuse 46 0.026
595
RMS001 Rem Sleep Behavior Disorder 46 0.026
596
c GNR039 Generalized Epilepsy with Febrile Seizures Plus, Type 2 46 0.026
597
c MLG068 Malignant Glioma 46 0.026
598
MXD026 Mixed Glioma 45 0.026
599
P MGL013 Megalencephaly 45 0.026
600
ORL013 Oral Lichen Planus 45 0.026
601
c CNT015 Central Sleep Apnea 45 0.026
602
CRB004 Cerebral Artery Occlusion 45 0.026
603
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.026
604
APL023 Aplasia Cutis Congenita, Nonsyndromic 45 0.026
605
PRT019 Protein-Losing Enteropathy 45 0.026
606
PNC056 Pineocytoma 45 0.026
607
ACT003 Acute Kidney Tubular Necrosis 45 0.026
608
IMP006 Impulse Control Disorder 45 0.026
609
P SBR004 Seborrheic Dermatitis 45 0.026
610
ASP008 Aspiration Pneumonitis 45 0.026
611
c CHR086 Chronic Conjunctivitis 45 0.026
612
CSL001 Causalgia 45 0.026
613
ORG002 Organic Acidemia 44 0.026
614
CNN002 Cannabis Abuse 44 0.026
615
DWR001 Dwarfism 44 0.026
616
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.026
617
c PRM038 Primary Agammaglobulinemia 44 0.026
618
HPT082 Hepatic Adenomas, Familial 44 0.026
619
c SPR086 Spermatogenic Failure 3 44 0.026
620
BCT021 Bacterial Sepsis 44 0.026
621
ANP009 Anaplastic Oligodendroglioma 43 0.026
622
c EPL026 Epileptic Encephalopathy, Early Infantile, 3 43 0.026
623
SPC005 Speech Disorder 43 0.026
624
P HRD018 Hair Disease 43 0.026
625
PMP004 Pemphigus Foliaceus 43 0.026
626
VRL003 Variola Major 42 0.026
627
BNS003 Binswanger's Disease 42 0.026
628
DNT014 Dental Pulp Disease 42 0.026
629
P CLS010 Cluster Headache 42 0.026
630
LRY017 Laryngeal Disease 42 0.026
631
EST005 Esotropia 42 0.026
632
MNN017 Mononeuropathy 42 0.026
633
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.026
634
GLC096 Galactorrhea 42 0.026
635
BTN002 Boutonneuse Fever 42 0.026
636
LPM010 Lipomatosis, Multiple Symmetric 42 0.026
637
MYF002 Myofascial Pain Syndrome 42 0.026
638
EPC002 Epicondylitis 41 0.026
639
LMB024 Limbic Encephalitis 41 0.026
640
LCH016 Lichen Sclerosus Et Atrophicus 41 0.026
641
P HYP263 Hypersomnia 41 0.026
642
PLY021 Polyradiculopathy 41 0.026
643
INT046 Intestinal Tuberculosis 41 0.026
644
P BLL007 Bullous Skin Disease 41 0.026
645
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.026
646
RDN001 Reading Disorder 40 0.026
647
ANX004 Anoxia 40 0.026
648
ANG049 Angioedema Induced by Ace Inhibitors 40 0.026
649
EPC005 Epicanthus 40 0.026
650
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.026
651
SLC004 Selective Igg Deficiency Disease 40 0.026
652
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 0.026
653
ALG001 Algoneurodystrophy 39 0.026
654
ADP007 Adie Pupil 39 0.026
655
ALL014 Allergic Encephalomyelitis 38 0.026
656
HYP264 Hypertonia 38 0.026
657
DTR001 Detrusor Sphincter Dyssynergia 38 0.026
658
VSM001 Vasomotor Rhinitis 38 0.026
659
P SYR003 Syringoma 37 0.026
660
c BLP048 Blepharospasm, Benign Essential 37 0.026
661
P CRB088 Cerebral Atrophy 37 0.026
662
c PRX088 Paroxysmal Nonkinesigenic Dyskinesia 1 37 0.026
663
PNB004 Panbronchiolitis, Diffuse 37 0.026
664
BLP004 Blepharophimosis 37 0.026
665
KKC001 Kikuchi Disease 36 0.026
666
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 36 0.026
667
TRG003 Trigeminal Nerve Disease 36 0.026
668
c MYC068 Myoclonic Epilepsy of Infancy 36 0.026
670
P NRM006 Neuromuscular Junction Disease 35 0.026
671
OLG006 Oligoastrocytoma 35 0.026
672
PCT001 Pectus Carinatum 35 0.026
673
ACR062 Acroosteolysis 35 0.026
674
WBR001 Weber Syndrome 35 0.026
675
NRD001 Neurodermatitis 35 0.026
676
c GLM025 Glioma Susceptibility 2 34 0.026
677
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.026
678
c ADL008 Adult Oligodendroglioma 34 0.026
679
c RST012 Restless Legs Syndrome 1 34 0.026
680
IMM044 Immunoglobulin G Deficiency 33 0.026
681
SGT001 Sagittal Sinus Thrombosis 32 0.026
682
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.026
683
PLN007 Plantar Fasciitis 32 0.026
684
c ATR031 Atrial Septal Defect 4 32 0.026
685
INF009 Inflammatory Spondylopathy 31 0.026
686
SPN011 Spongiotic Dermatitis 31 0.026
687
ATY003 Atypical Autism 31 0.026
688
ERL030 Early-Onset Generalized Limb-Onset Dystonia 31 0.026
689
CHR281 Chronic Hiccups 31 0.026
690
MNC001 Monocular Esotropia 30 0.026
691
SNG003 Single Ventricular Heart 30 0.026
693
PDP001 Pedophilia 30 0.026
694
DPN001 Dependent Personality Disorder 30 0.026
695
GRN006 Granulomatous Angiitis 30 0.026
696
P TRC024 Trachea Carcinoma 30 0.026
697
TLG001 Telogen Effluvium 30 0.026
698
HLS001 Heel Spur 30 0.026
699
ANP008 Anaplastic Oligoastrocytoma 30 0.026
700
FTL007 Fetal Hydantoin Syndrome 29 0.026
701
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.026
702
MRL006 Meralgia Paraesthetica, Familial 29 0.026
703
PST092 Posttransplant Acute Limbic Encephalitis 29 0.026
704
MNC004 Monoclonal Paraproteinemia 28 0.026
705
ATH004 Athetosis 28 0.026
706
PRN017 Perianal Hematoma 28 0.026
707
SRN002 Sirenomelia 28 0.026
708
SGM008 Segmental Dystonia 28 0.026
709
PRP015 Paraphilia Disorder 27 0.026
710
HNM002 Hinman Syndrome 27 0.026
711
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.026
712
AMY005 Amyloid Neuropathy 26 0.026
713
P PLM069 Pulmonary Venous Return Anomaly 26 0.026
714
SHP003 Shapiro Syndrome 26 0.026
715
FTL073 Fetal Anticonvulsant Syndrome 26 0.026
716
TRN011 Transient Refractive Change 25 0.026
717
ESN016 Eosinophilic Pustular Folliculitis 25 0.026
718
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.026
719
ESN022 Eosinophilic Colitis 25 0.026
720
c SZR014 Seizures, Benign Familial Infantile, 1 25 0.026
721
OCC008 Occipital Neuralgia 25 0.026
722
EXH001 Exhibitionism 24 0.026
723
P PHC014 Phocomelia 24 0.026
724
HYP144 Hyperacusis 23 0.026
725
FCL074 Facial Spasm 23 0.026
726
ADS003 Aids Phobia 23 0.026
727
EPL011 Epilepsy, Benign Occipital 23 0.026
728
CHR158 Charles Bonnet Syndrome 23 0.026
729
URM001 Uremic Neuropathy 22 0.026
730
PST047 Post-Traumatic Epilepsy 22 0.026
731
HML018 Homologous Wasting Disease 22 0.026
732
CRB023 Cerebellopontine Angle Meningioma 21 0.026
733
SLF017 Sulfamethoxazole Allergy 20 0.026
734
CD4008 Cd4/cd8 T-Cell Ratio 20 0.026
735
SCN067 Scn1a Seizure Disorders 19 0.026
736
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 18 0.026
737
LTH043 Lithium Transport 18 0.026
738
CNV009 Convulsions Benign Familial Neonatal Dominant Form 17 0.026
739
SGC002 Sgce Myoclonus-Dystonia 17 0.026
740
CRM010 Cramp-Fasciculation Syndrome 16 0.026
741
ORG003 Organic Mood Syndrome 14 0.026
743
DPH028 Diaphragmatic Flutter 13 0.026
744
CRB080 Cor Biloculare 11 0.026
746
RRP007 Rare Paroxysmal Movement Disorder 7 0.026
Content
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