Search results for Glutamic acid

1401 hits were found for Glutamic acid

# Family MCID Name MIFTS Score
1
GLT033 Glutamic Acid Decarboxylase, Brain, Membrane Form 4 2.324
2
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 26 2.295
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.430
4
P SZR006 Seizure Disorder 58 0.406
5
VSL002 Visual Epilepsy 58 0.397
6
HLX001 Helix Syndrome 47 0.379
7
P LVR013 Liver Disease 68 0.364
8
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.347
9
P LTR001 Lateral Sclerosis 53 0.347
10
P NRB001 Neuroblastoma 71 0.337
11
PRT037 Pertussis 65 0.337
12
ISC004 Ischemia 60 0.331
13
P GLM045 Glioma 63 0.329
14
GLL048 Glial Tumor 45 0.320
15
P HNT016 Huntington Disease 71 0.303
16
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.300
17
HYP056 Hypoglycemia 66 0.299
18
P ENC018 Encephalopathy 61 0.294
19
P SCH015 Schizophrenia 75 0.292
20
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.289
21
DPR016 Depression 63 0.284
22
FTT001 Fatty Liver Disease 61 0.283
23
P ALZ034 Alzheimer Disease 88 0.276
24
HPT004 Hepatic Coma 43 0.272
25
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.266
26
TRM010 Traumatic Brain Injury 53 0.266
27
HYP060 Hyperinsulinism 54 0.261
28
LVR012 Liver Cirrhosis 63 0.260
29
MNT002 Mental Depression 57 0.260
30
P BPL003 Bipolar Disorder 56 0.259
31
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.258
32
48X005 48,xyyy 39 0.258
33
c MJR024 Major Affective Disorder 9 41 0.256
34
c MJR022 Major Affective Disorder 8 38 0.256
35
ATM095 Autoimmune Disease 61 0.256
36
STT001 Status Epilepticus 59 0.254
37
BRN071 Brain Injury 49 0.251
38
P CLR023 Colorectal Cancer 98 0.250
39
CHL068 Cholestasis 60 0.249
40
HYP266 Hypoxia 56 0.248
41
ALC007 Alcohol Dependence 66 0.248
42
ALL026 Allergic Hypersensitivity Disease 64 0.246
43
CRB004 Cerebral Artery Occlusion 44 0.246
44
P TMP001 Temporal Lobe Epilepsy 50 0.245
45
MTB004 Metabolic Acidosis 50 0.244
46
GLB015 Glioblastoma Multiforme 75 0.243
47
OCL069 Ocular Motor Apraxia 51 0.243
48
HPT019 Hepatic Encephalopathy 60 0.243
49
P MJR001 Major Depressive Disorder 68 0.239
50
NRL016 Neural Tube Defects 82 0.239
51
HYP066 Hyperglycemia 61 0.238
52
P ATS364 Autism 65 0.237
53
SPN186 Spinal Cord Injury 60 0.237
54
P EPL164 Epilepsy 71 0.234
55
P DRR001 Diarrhea 57 0.233
56
P ENC004 Encephalitis 61 0.232
57
ANX004 Anoxia 42 0.228
58
P BRS047 Breast Cancer 96 0.228
59
LPD008 Lipid Metabolism Disorder 62 0.228
60
MDD011 Mood Disorder 62 0.227
61
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.226
62
P KDN018 Kidney Disease 70 0.225
63
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.220
64
c ATS007 Autism Spectrum Disorder 67 0.219
65
GST092 Gastroesophageal Reflux 65 0.216
66
BNR002 Bone Resorption Disease 48 0.215
67
P NRP001 Neuropathy 56 0.214
68
HYP014 Hyperuricemia 51 0.213
69
STF001 Stiff-Person Syndrome 60 0.212
70
ANX010 Anxiety 72 0.210
71
P PRS040 Prostate Cancer 97 0.208
72
CHL014 Cholera 55 0.208
73
P CHR345 Chronic Pain 50 0.207
74
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.206
75
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.204
76
TTN003 Tetanus 64 0.204
77
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.204
78
c MGR028 Migraine with or Without Aura 1 69 0.203
79
P HPT023 Hepatocellular Carcinoma 100 0.201
80
ACR006 Aceruloplasminemia 73 0.198
81
P CRN300 Coronary Heart Disease 1 63 0.198
82
P LKM002 Leukemia 66 0.195
83
OST012 Osteoarthritis 78 0.194
84
P DDN001 Duodenal Ulcer 50 0.193
85
P CRN018 Coronary Artery Anomaly 63 0.193
86
P HYP750 Hypertriglyceridemia, Familial 61 0.193
87
CLT003 Colitis 62 0.190
88
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.188
89
PLM001 Pulmonary Tuberculosis 70 0.187
90
ALL014 Allergic Encephalomyelitis 39 0.186
91
P INF037 Inflammatory Bowel Disease 56 0.185
92
P VSC007 Vascular Disease 63 0.182
93
GT001 Gout 63 0.181
94
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.181
95
P DBT009 Diabetes Mellitus 64 0.181
96
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.180
97
47X002 47,xyy 49 0.180
98
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.179
99
PPL052 Papillomatosis, Confluent and Reticulated 34 0.179
100
DFC004 Deficiency Anemia 75 0.179
101
HMN044 Human Immunodeficiency Virus Type 1 71 0.177
102
CRB039 Cerebrovascular Disease 69 0.176
103
P MLT020 Multiple Sclerosis 72 0.176
104
DRM006 Dermatitis 61 0.174
105
BRN004 Brain Edema 55 0.173
106
P PNC035 Pancreatic Cancer 84 0.173
107
ATH013 Atherosclerosis Susceptibility 66 0.173
108
P OVR042 Ovarian Cancer 89 0.173
109
P TRM003 Tremor 53 0.172
110
P PHC003 Pheochromocytoma 71 0.171
111
CYT002 Cytokine Deficiency 44 0.171
112
P HYP086 Hypothyroidism 68 0.171
113
P NRF023 Neurofibromatosis, Type Ii 76 0.170
114
ADR040 Adrenal Gland Pheochromocytoma 46 0.170
115
P ADN016 Adenocarcinoma 64 0.169
116
ART140 Arteries, Anomalies of 53 0.169
117
STR067 Stroke, Ischemic 80 0.169
118
P PRP019 Peripheral Nervous System Disease 57 0.168
119
P HRP006 Herpes Simplex 65 0.167
120
c HYP836 Hypercholesterolemia, Familial, 1 72 0.167
121
HRW001 Hair Whorl 36 0.166
122
P FRG001 Fragile X Syndrome 68 0.166
123
INS024 Insulin-Like Growth Factor I 79 0.164
124
P GST044 Gastritis 55 0.164
125
HMC014 Homocysteinemia 53 0.163
126
P LNG032 Lung Cancer 97 0.163
127
NNL006 Non-Alcoholic Steatohepatitis 51 0.161
128
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.160
129
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.160
130
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.160
131
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.160
132
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.160
133
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.160
134
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.160
135
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.160
136
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.160
137
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.160
138
ULC004 Ulcerative Colitis 73 0.160
139
GLC003 Glucose Intolerance 54 0.160
140
P ALC033 Alcohol Use Disorder 58 0.160
141
P HRT032 Heart Disease 75 0.160
142
P MYC007 Myocardial Infarction 70 0.159
143
CYS001 Cystic Fibrosis 80 0.159
144
PNG002 Pain Agnosia 51 0.158
145
c SYS001 Systemic Lupus Erythematosus 86 0.157
146
P MCR115 Microvascular Complications of Diabetes 5 66 0.157
147
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.155
148
P MYP004 Myopathy 64 0.154
149
IRN002 Iron Metabolism Disease 57 0.154
150
P CRD119 Cardiac Arrest 67 0.154
151
OBS002 Obsessive-Compulsive Disorder 68 0.154
152
P BLD134 Bladder Cancer 78 0.153
153
c ACT075 Acute Myocardial Infarction 56 0.153
154
P MSC005 Muscular Dystrophy 66 0.153
155
P OST002 Osteoporosis 73 0.153
156
P LYM031 Lymphocytic Leukemia 55 0.152
157
P PSR002 Psoriasis 62 0.152
158
AMN003 Amnestic Disorder 54 0.152
159
OST159 Osteogenic Sarcoma 66 0.151
160
PST011 Pustulosis of Palm and Sole 52 0.151
161
ADN018 Adenoma 58 0.151
162
c CHR684 Chronic Kidney Disease 66 0.150
163
c HYP595 Hypertension, Essential 84 0.148
164
P GST053 Gastric Cancer 83 0.148
165
P AST007 Astrocytoma 50 0.148
166
EMB004 Embryonal Carcinoma 57 0.147
167
P ESP024 Esophagitis 62 0.147
168
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.147
169
LMB024 Limbic Encephalitis 41 0.147
170
P PRK057 Parkinson Disease, Late-Onset 76 0.147
171
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.147
172
c ACT134 Acute Liver Failure 51 0.146
173
c PRC016 Pre-Eclampsia 63 0.145
174
DWN001 Down Syndrome 70 0.145
175
c VRL010 Viral Hepatitis 51 0.144
176
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.143
177
P MYL006 Myeloid Leukemia 60 0.143
178
P LPS004 Lupus Erythematosus 61 0.143
179
CNG034 Congestive Heart Failure 70 0.142
180
AGN016 Aging 56 0.142
181
P RTN016 Retinal Degeneration 53 0.140
182
c MLG068 Malignant Glioma 45 0.140
183
MLN008 Melanoma 69 0.140
184
P DRM053 Dermatitis, Atopic 66 0.139
185
P HDC001 Headache 57 0.139
186
PHN003 Phenylketonuria 75 0.139
187
NTR005 Nutritional Deficiency Disease 61 0.139
188
URM002 Uremia 49 0.139
189
P MNN013 Meningitis 65 0.137
190
URT049 Urate Oxidase, Pseudogene 25 0.136
191
MYL069 Myeloma, Multiple 85 0.136
192
P DMN002 Dementia 67 0.136
193
VCC001 Vaccinia 49 0.135
194
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.135
195
HDN002 Head Injury 45 0.135
196
DBT010 Diabetic Neuropathy 55 0.134
197
IMM167 Immune Deficiency Disease 78 0.133
198
PSY004 Psychotic Disorder 67 0.133
199
P CRD246 Cardiovascular System Disease 56 0.132
200
P BND020 Bone Disease 59 0.132
201
P CTR002 Cataract 60 0.132
202
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.132
203
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.132
204
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.132
205
P LCT001 Lactic Acidosis 51 0.131
206
P BCL017 B-Cell Lymphoma 58 0.131
207
LNG099 Lung Disease 61 0.131
208
c HPT073 Hepatitis C Virus 70 0.130
209
c PCH010 Pachyonychia Congenita 3 43 0.129
210
P MPL001 Maple Syrup Urine Disease 69 0.129
211
CRV035 Cervical Cancer 76 0.129
212
c LKM061 Leukemia, Acute Myeloid 83 0.128
213
SQM006 Squamous Cell Carcinoma 60 0.128
214
SKN016 Skin Disease 63 0.128
215
PLY150 Polykaryocytosis Inducer 31 0.128
216
c RHB024 Rhabdomyosarcoma 2 65 0.128
217
END030 End Stage Renal Failure 58 0.127
218
c ACT027 Acute Pancreatitis 59 0.127
219
BCT022 Bacterial Infectious Disease 56 0.127
220
P RTN024 Retinoblastoma 72 0.127
221
c FML008 Familial Retinoblastoma 53 0.127
222
TRN015 Transient Cerebral Ischemia 62 0.126
223
P TRN020 Turner Syndrome 65 0.126
224
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.125
225
SVR004 Severe Combined Immunodeficiency 73 0.125
226
TRT001 Teratocarcinoma 46 0.125
227
WTH001 Withdrawal Disorder 48 0.124
228
CHR073 Choreatic Disease 52 0.124
229
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.124
230
CLF027 Cleft Palate, Isolated 64 0.124
231
c SML038 Small Cell Cancer of the Lung 65 0.123
232
P DYS154 Dystonia 65 0.123
233
GST033 Gestational Diabetes 57 0.123
234
INS001 Insulinoma 60 0.123
235
P MYC033 Myoclonus 46 0.122
236
ADG002 Audiogenic Seizures 26 0.122
237
END040 Endogenous Depression 54 0.122
238
CRH001 Crohn's Disease 74 0.122
239
P PRD008 Periodontitis 62 0.122
240
HMP009 Haemophilus Influenzae 42 0.122
241
RYS001 Reye Syndrome 51 0.120
242
P RSP003 Respiratory Failure 74 0.120
243
c INH020 Inherited Metabolic Disorder 46 0.120
244
P HYP076 Hyperthyroidism 55 0.119
245
c ACT071 Acute Kidney Failure 59 0.119
246
CHL123 Chlamydia 59 0.119
247
FCL014 Focal Epilepsy 54 0.119
248
FBR047 Fibromyalgia 59 0.118
249
RCK004 Rickets 69 0.118
250
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.118
251
P RHN004 Rhinitis 57 0.117
252
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.117
253
P ART022 Arthritis 70 0.117
254
AST005 Asthma 77 0.117
255
IRR002 Irritable Bowel Syndrome 63 0.117
256
PLM010 Pulmonary Edema 55 0.116
257
P MVM001 Movement Disease 61 0.116
258
DPH001 Diphtheria 60 0.115
259
P MTR014 Motor Neuron Disease 64 0.115
260
ANT024 Anthrax Disease 58 0.113
261
SRC014 Sarcoma 65 0.113
262
SPN035 Spindle Cell Sarcoma 51 0.113
263
ACQ007 Acquired Immunodeficiency Syndrome 60 0.113
264
P HPT021 Hepatitis 67 0.113
265
P MSC003 Muscular Atrophy 52 0.113
266
PRN011 Pernicious Anemia 52 0.113
267
BRR014 Barrett Esophagus 64 0.113
268
P PNC044 Pancreatitis 61 0.113
269
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.112
270
ADL002 Adult Syndrome 69 0.112
271
KRT009 Keratosis 53 0.112
272
STM007 Stomatitis 49 0.111
273
P FBR017 Fibrosarcoma 56 0.111
274
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.111
275
c MCR120 Microvascular Complications of Diabetes 7 47 0.111
276
c MCR113 Microvascular Complications of Diabetes 3 52 0.111
277
RTN023 Retinitis 46 0.111
278
NRR001 Neuroretinitis 43 0.111
279
BRN028 Brain Cancer 73 0.111
280
c MCR130 Microvascular Complications of Diabetes 6 41 0.110
281
c MCR133 Microvascular Complications of Diabetes 4 41 0.110
282
HNS001 Hansen's Disease 34 0.109
283
ANG054 Angina Pectoris 66 0.109
284
P LPR021 Leprosy 3 67 0.109
285
THY029 Thyroid Carcinoma 59 0.109
286
P INF038 Influenza 68 0.109
287
P BRS044 Breast Adenocarcinoma 59 0.109
288
P RTN008 Retinitis Pigmentosa 77 0.108
290
P LKM062 Leukemia, Acute Lymphoblastic 68 0.108
291
P LNG064 Lung Cancer Susceptibility 3 77 0.108
292
THR024 Thrombosis 56 0.107
293
CRB037 Cerebral Palsy 68 0.107
294
CLN015 Colon Adenocarcinoma 63 0.106
295
P OVR082 Overgrowth Syndrome 50 0.106
296
ALL003 Allergic Rhinitis 67 0.106
297
P OBS001 Obstructive Jaundice 48 0.106
298
P SKN015 Skin Carcinoma 67 0.106
299
HLC007 Helicobacter Pylori Infection 59 0.106
300
P ART021 Arteriosclerosis 54 0.106
301
SBC016 Subacute Delirium 44 0.106
302
P RTN018 Retinal Disease 52 0.105
303
RHM027 Rheumatic Disease 56 0.105
304
PRT036 Peritonitis 65 0.105
305
HYP005 Hypokalemia 55 0.105
306
CNS004 Constipation 57 0.105
307
P GLM040 Glioma Susceptibility 1 81 0.104
308
P BRB001 Beriberi 44 0.104
309
CRT015 Carotid Artery Occlusion 44 0.104
310
P HYP265 Hypotonia 42 0.103
311
NRT001 Neurotic Disorder 52 0.103
312
VSC002 Vascular Dementia 57 0.103
313
P CYS018 Cystitis 59 0.103
314
MYL009 Myelodysplastic Syndrome 70 0.103
315
P LYM118 Lymphoma 68 0.103
316
c THR092 Thrombophilia Due to Thrombin Defect 73 0.102
317
P ATR011 Atrial Fibrillation 66 0.102
318
MNS015 Monosodium Glutamate Sensitivity 20 0.102
319
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.102
320
GST050 Gastrointestinal System Disease 56 0.102
321
PRS045 Prostatic Hypertrophy 52 0.102
322
c DWL002 Dowling-Degos Disease 1 58 0.101
323
DNT012 Dental Caries 51 0.101
324
P SBS003 Substance Abuse 54 0.101
325
MTH071 Methane Production 26 0.101
326
P THR014 Thrombocytopenia 68 0.100
327
P MTH008 Methylmalonic Acidemia 51 0.100
328
DMY004 Demyelinating Disease 52 0.099
329
ATS010 Autosomal Recessive Disease 48 0.099
330
P GRV001 Graves' Disease 55 0.099
331
P PLY019 Polyneuropathy 56 0.099
332
LPT014 Leptin Deficiency or Dysfunction 73 0.099
333
ARG004 Argyria 28 0.099
334
P PRS038 Personality Disorder 65 0.099
335
MTH009 Mouth Disease 56 0.098
336
RTN003 Retinal Ischemia 50 0.098
337
INT007 Intermediate Coronary Syndrome 55 0.098
338
c ACT073 Acute Leukemia 58 0.098
339
LYM133 Lymphoma, Hodgkin, Classic 69 0.097
340
P MDL005 Medulloblastoma 77 0.097
341
MLR004 Malaria 80 0.097
342
CNT047 Contact Dermatitis 57 0.097
343
PPT001 Peptic Esophagitis 51 0.097
344
P INS002 in Situ Carcinoma 52 0.096
345
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.096
346
CRV045 Cervical Intraepithelial Neoplasia 39 0.096
347
P MJR007 Major Affective Disorder 1 43 0.096
348
c HPT001 Hepatitis C 63 0.096
349
PTH003 Pathologic Nystagmus 51 0.096
350
P CNR004 Cone-Rod Dystrophy 2 71 0.095
351
ACT084 Acute Stress Disorder 48 0.095
352
c BRN108 Branchiootic Syndrome 1 61 0.095
353
c PRS136 Prostate Cancer, Hereditary, 6 33 0.095
354
c PRS130 Prostate Cancer, Hereditary, 8 32 0.095
355
PST028 Post-Traumatic Stress Disorder 58 0.095
356
TXC005 Toxic Shock Syndrome 61 0.095
357
P ECL001 Eclampsia 51 0.094
358
ORL011 Oral Cancer 60 0.094
359
P KDN017 Kidney Cancer 61 0.094
360
CHL004 Cholelithiasis 49 0.094
361
CHL079 Children's Interstitial Lung Disease 27 0.093
362
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.093
363
P PLM037 Pulmonary Hypertension 68 0.093
364
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.093
365
ENT004 Enthesopathy 48 0.093
366
GLT005 Glutamate Formiminotransferase Deficiency 35 0.093
367
P HYP098 Hypereosinophilic Syndrome 66 0.093
368
ATX019 Ataxia with Vitamin E Deficiency 48 0.093
369
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.093
370
NWC001 Newcastle Disease 44 0.093
371
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.092
372
KRT002 Keratomalacia 48 0.092
373
P THY032 Thyroiditis 53 0.092
374
BLR008 Bilirubin Metabolic Disorder 57 0.092
375
PRS021 Prostatic Adenoma 51 0.092
376
TBC004 Tobacco Addiction 64 0.092
377
MSL001 Measles 61 0.092
378
P URT039 Urticaria 58 0.092
379
P HYD006 Hydrocephalus 65 0.092
380
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.091
381
P SLP006 Sleep Apnea 69 0.091
382
LYM019 Lymphosarcoma 47 0.091
383
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 53 0.091
384
P NRV007 Nervous System Disease 66 0.091
385
SPS057 Spasticity 41 0.091
386
CRB090 Cerebral Hypoxia 43 0.090
387
EYD002 Eye Disease 58 0.090
388
P INF032 Infertility 57 0.090
389
P ALP008 Alopecia 56 0.090
390
CHL067 Cholecystitis 58 0.090
391
TBR011 Tuberculous Meningitis 48 0.089
392
P PNC025 Panic Disorder 53 0.089
393
MNG007 Manganese Poisoning 29 0.089
394
SCH014 Schistosomiasis 56 0.089
395
P AMY004 Amyloidosis 70 0.089
396
P RHB003 Rhabdomyosarcoma 62 0.089
397
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.089
398
P CND004 Candidiasis 57 0.089
399
LSH001 Leishmaniasis 63 0.089
400
P KLZ004 Kala-Azar 1 41 0.089
401
P MYC084 Mycobacterium Tuberculosis 1 68 0.088
402
MRP001 Morphine Dependence 41 0.088
403
AMN006 Aminoaciduria 38 0.088
404
c MCR129 Microvascular Complications of Diabetes 1 66 0.088
405
P OPT006 Optic Nerve Disease 57 0.088
406
P ART023 Arthropathy 62 0.088
407
SPP010 Suppressor of Tumorigenicity 3 51 0.088
408
c BCT007 Bacterial Meningitis 55 0.087
409
PRP027 Peripheral Vascular Disease 71 0.087
410
c CNT035 Central Nervous System Disease 54 0.087
411
PRP001 Propionic Acidemia 66 0.087
412
PST092 Posttransplant Acute Limbic Encephalitis 29 0.087
413
P TBR001 Tuberous Sclerosis 70 0.087
414
P INT143 Interstitial Cystitis 61 0.087
415
P EXN002 Exanthem 57 0.086
416
c PNS012 Paine Syndrome 61 0.086
417
c ATR087 Atrial Standstill 1 74 0.086
418
END057 Endometrial Cancer 74 0.086
419
ORL015 Oral Squamous Cell Carcinoma 43 0.086
420
c ATM075 Autoimmune Encephalitis 38 0.086
421
SCH012 Schizoaffective Disorder 50 0.086
422
c SVR001 Severe Acute Respiratory Syndrome 55 0.086
423
ENT011 Enterocolitis 50 0.086
424
P CLC063 Celiac Disease 1 68 0.086
425
RTN017 Retinal Detachment 60 0.086
426
c HPT016 Hepatitis B 59 0.086
427
c LRG017 Large Intestine Cancer 47 0.085
428
TRD006 Tardive Dyskinesia 55 0.085
429
P NSP012 Nasopharyngeal Carcinoma 67 0.085
430
PRP016 Paraplegia 53 0.085
431
ATN004 Autonomic Neuropathy 44 0.085
432
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.085
433
ISL099 Isolated Methylmalonic Acidemia 30 0.085
434
P NMN002 Niemann-Pick Disease 60 0.085
435
P NPH012 Nephrotic Syndrome 63 0.085
436
P MGL001 Megaloblastic Anemia 55 0.085
437
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.084
438
c FNC043 Fanconi Anemia, Complementation Group E 62 0.084
439
HMS001 Hemosiderosis 54 0.084
440
TND005 Tendinitis 52 0.084
441
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.084
442
DRG003 Drug Dependence 47 0.084
443
P CNJ013 Conjunctivitis 65 0.084
444
P OLV001 Olivopontocerebellar Atrophy 52 0.084
445
KPS004 Kaposi Sarcoma 75 0.084
446
IDP011 Idiopathic Interstitial Pneumonia 63 0.084
447
P PLM036 Pulmonary Fibrosis 61 0.084
448
GST045 Gastroenteritis 59 0.084
449
PRS129 Prostatic Hyperplasia, Benign 49 0.084
450
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.083
451
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.083
452
RRS014 Rare Surgical Neurologic Disease 32 0.083
453
OPT003 Opiate Dependence 50 0.083
454
P RRH023 Rare Hereditary Hemochromatosis 41 0.083
455
MLT157 Multiple System Atrophy 1 70 0.083
456
P THL005 Thalassemia 60 0.082
457
INT075 Intracranial Hypertension 53 0.082
458
ALL006 Allergic Asthma 56 0.082
459
CLR108 Colorectal Adenoma 64 0.082
460
P HML002 Hemolytic Anemia 62 0.081
461
LNG031 Lung Benign Neoplasm 50 0.081
462
PLS009 Plasma Cell Neoplasm 51 0.081
463
CHR178 Chromosomal Triplication 35 0.081
464
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.081
465
FDL002 Food Allergy 49 0.081
466
ASP026 Asplenia, Isolated Congenital 44 0.081
467
CHL065 Cholangiocarcinoma 67 0.081
468
P RTT002 Rett Syndrome 80 0.081
469
RNL077 Renal Fibrosis 47 0.081
470
c MJR003 Major Affective Disorder 6 33 0.080
471
c MJR006 Major Affective Disorder 5 33 0.080
472
P VSC011 Vasculitis 62 0.080
473
CHG001 Chagas Disease 66 0.080
474
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.080
475
HND015 Hand Skill, Relative 33 0.080
476
IRN001 Iron Deficiency Anemia 58 0.080
477
INT079 Intrahepatic Cholangiocarcinoma 50 0.080
478
BLR001 Biliary Atresia 50 0.080
479
c LKM071 Leukemia, Chronic Lymphocytic 79 0.079
480
P TRT010 Teratoma 51 0.079
481
P PYL005 Pyelonephritis 56 0.079
482
P FTL001 Fetal Alcohol Syndrome 55 0.079
483
CCN001 Cocaine Dependence 48 0.079
484
CHR074 Choriocarcinoma 46 0.079
485
SCR011 Scrapie 38 0.079
486
P END044 Endometriosis 62 0.079
487
P BNG032 Benign Mesothelioma 45 0.079
488
MSC157 Muscular Dystrophy, Duchenne Type 71 0.079
489
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.078
490
PLM031 Poliomyelitis 57 0.078
491
P SYS005 Systemic Scleroderma 70 0.078
492
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.078
493
P FBR031 Febrile Seizures 51 0.078
494
ANR007 Anorexia Nervosa 63 0.078
495
P PRN023 Prion Disease 57 0.078
496
CYS013 Cystinuria 62 0.078
497
P SLP005 Sleep Disorder 59 0.078
498
PRV004 Periventricular Leukomalacia 51 0.077
499
TYP007 Typhoid Fever 63 0.077
500
P SCK005 Sickle Cell Disease 50 0.077
501
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.077
502
DCR008 Dicarboxylic Aminoaciduria 44 0.077
503
c MJR008 Major Affective Disorder 2 34 0.077
504
c MJR023 Major Affective Disorder 7 33 0.077
505
c MJR004 Major Affective Disorder 4 28 0.077
506
PRT013 Portal Hypertension 60 0.076
507
HYP081 Hypolipoproteinemia 50 0.076
508
P INT068 Intestinal Disease 52 0.076
509
GTR002 Goiter 52 0.076
510
TND004 Tendinopathy 44 0.076
511
P HMC002 Homocystinuria 54 0.076
512
MNN009 Meningoencephalitis 49 0.076
513
HSH003 Hashimoto Thyroiditis 62 0.076
514
ETN001 Eating Disorder 59 0.075
515
DYS073 Dysphagia 50 0.075
516
JPN002 Japanese Encephalitis 54 0.075
517
MNN042 Meningioma, Radiation-Induced 62 0.075
518
P BNC003 Bone Cancer 57 0.075
519
c MNN043 Meningioma, Familial 74 0.075
520
P SRC025 Sarcoidosis 1 70 0.075
521
c DLT002 Dilated Cardiomyopathy 79 0.075
522
LYS002 Lysosomal Storage Disease 52 0.075
523
HYP080 Hypogonadism 50 0.075
524
ARG002 Argininosuccinic Aciduria 60 0.074
525
DSS008 Disease of Mental Health 57 0.074
526
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.074
527
SPN021 Spinal Meningioma 47 0.074
528
SCR001 Secretory Meningioma 37 0.074
529
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.074
530
HYP064 Hypogonadotropism 40 0.074
531
c TBR025 Tuberous Sclerosis 1 76 0.074
533
ANN002 Anencephaly 55 0.074
534
CTR172 Citrullinemia, Classic 64 0.074
535
GLL008 Gilles De La Tourette Syndrome 66 0.074
536
PRT038 Protein-Energy Malnutrition 54 0.074
537
P NRC002 Narcolepsy 51 0.073
538
c PRM038 Primary Agammaglobulinemia 43 0.073
539
BRK010 Burkitt Lymphoma 67 0.073
540
P MLN007 Male Infertility 56 0.073
541
P MYS003 Myasthenia Gravis 68 0.073
542
P ATR005 Atrophic Gastritis 50 0.073
543
P RST001 Restless Legs Syndrome 54 0.073
544
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.073
545
P TCL004 T-Cell Leukemia 47 0.073
546
LRN003 Learning Disability 49 0.073
547
P SCL018 Scoliosis 60 0.073
548
IGR001 Ige Responsiveness, Atopic 59 0.073
549
P MYC008 Myocarditis 59 0.072
550
P FRN006 Frontotemporal Dementia 70 0.072
551
MSC007 Muscle Hypertrophy 63 0.071
552
SPN050 Spinocerebellar Degeneration 41 0.071
553
OPD006 Opioid Addiction 48 0.071
554
THY030 Thyroid Gland Disease 51 0.071
555
PLG002 Plague 57 0.070
556
P GRF003 Graft-Versus-Host Disease 71 0.070
557
OTT002 Otitis Media 71 0.070
558
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.070
559
PYR009 Pyridoxine Deficiency Anemia 34 0.070
560
P SPN046 Spinal Muscular Atrophy 64 0.070
561
ERL001 Early Myoclonic Encephalopathy 61 0.070
562
P SHR001 Short Bowel Syndrome 52 0.069
563
MXD026 Mixed Glioma 45 0.069
564
c WLM018 Wilms Tumor 5 62 0.069
565
P PLY018 Polycythemia 55 0.069
566
WST005 West Nile Virus 55 0.069
567
TLN003 Telangiectasis 51 0.069
568
c MCR112 Microvascular Complications of Diabetes 2 41 0.069
569
HVY002 Heavy Metal Poisoning 22 0.069
570
c SPN225 Spondyloarthropathy 1 73 0.069
571
OCL052 Ocular Dominance 41 0.069
572
RHM001 Rheumatic Fever 61 0.069
573
KRT006 Keratoconjunctivitis 53 0.069
574
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.069
575
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.068
576
SYN007 Synovitis 55 0.068
577
P CRB059 Cerebellar Degeneration 37 0.068
578
P SJG008 Sjogren Syndrome 56 0.068
579
HMP005 Hemiplegia 54 0.068
580
P THY023 Thymoma 65 0.068
581
c THY107 Thymoma, Familial 54 0.068
582
PNC129 Pancreatic Adenocarcinoma 67 0.068
583
CRC021 Carcinosarcoma 61 0.068
584
P DNG005 Dengue Virus 57 0.068
585
ATN005 Autonomic Dysfunction 47 0.068
586
PYR016 Pyridoxine Deficiency 30 0.068
587
CLF001 Cleft Lip 53 0.068
588
CLR109 Colorectal Adenocarcinoma 50 0.068
589
NCT003 N-Acetylglutamate Synthase Deficiency 44 0.068
590
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.068
591
c FML035 Familial Hyperlipidemia 55 0.068
592
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.067
593
CRT072 Creutzfeldt-Jakob Disease 69 0.067
594
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.067
595
SFT003 Soft Tissue Sarcoma 56 0.067
596
GNG013 Gingivitis 59 0.067
597
P PLY014 Polycystic Kidney Disease 59 0.067
598
CCN002 Cocaine Abuse 48 0.067
599
DBT002 Diabetic Autonomic Neuropathy 41 0.067
600
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.067
601
HRN029 Hearing Loss, Noise-Induced 37 0.067
602
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.067
604
P TYR004 Tyrosinemia 58 0.066
605
c PRD040 Periodontitis, Chronic 54 0.066
606
DYS015 Dysentery 50 0.066
607
PST021 Postpartum Depression 50 0.066
608
SCH003 Schizophreniform Disorder 56 0.066
609
OCL006 Ocular Hypertension 53 0.066
610
BRD004 Borderline Personality Disorder 53 0.066
611
VRC005 Varicose Veins 60 0.066
612
P SNS001 Sensorineural Hearing Loss 61 0.066
613
P MYS005 Myositis 56 0.066
614
P LKD001 Leukodystrophy 59 0.066
615
YLL002 Yellow Fever 60 0.065
616
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.065
617
P MCR010 Microcephaly 58 0.065
618
NRT004 Neuritis 53 0.065
619
PRS047 Prostatitis 56 0.065
620
TRN018 Transitional Cell Carcinoma 56 0.065
621
P HMP007 Hemophilia 51 0.064
622
KWS001 Kwashiorkor 45 0.064
623
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.064
624
P UVT001 Uveitis 57 0.064
625
c BTT014 Beta-Thalassemia 72 0.063
626
P EHL001 Ehlers-Danlos Syndrome 57 0.063
627
CRH005 Crohn's Colitis 52 0.063
628
c PRG106 Progressive Muscular Dystrophy 33 0.063
629
ANP008 Anaplastic Oligoastrocytoma 30 0.063
630
TXC002 Toxic Encephalopathy 52 0.063
631
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.063
632
ACN002 Acanthosis Nigricans 60 0.063
633
BRT054 Brittle Bone Disorder 70 0.062
634
P OLG002 Oligodendroglioma 67 0.062
635
DBT004 Diabetic Polyneuropathy 50 0.062
636
ALC006 Alcoholic Hepatitis 61 0.062
637
RBS001 Rabies 58 0.062
638
PRP080 Peripheral Artery Disease 53 0.062
639
P TRC086 Trichohepatoenteric Syndrome 1 59 0.062
640
c GRV008 Graves Disease 1 55 0.062
641
c ESS001 Essential Tremor 56 0.062
642
ANR040 Aneurysm 58 0.062
643
P ATX030 Ataxia-Telangiectasia 83 0.061
644
P SLL003 Salla Disease 48 0.061
645
EPD015 Epidemic Typhus 46 0.061
646
LMY002 Leiomyoma 50 0.061
647
LYM040 Lymphoblastic Lymphoma 54 0.061
648
P TCD001 Tic Disorder 54 0.061
649
P CTR177 Citrullinemia, Type Ii, Adult-Onset 46 0.061
650
SCK003 Sickle Cell Anemia 72 0.061
651
CRT017 Cartilage Disease 54 0.061
652
OVR094 Ovarian Epithelial Cancer 38 0.061
653
VRL011 Viral Infectious Disease 61 0.061
654
DWR001 Dwarfism 44 0.061
655
GLT035 Glutaric Acidemia I 48 0.061
656
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.060
657
INT002 Intermittent Claudication 61 0.060
658
CHC001 Chickenpox 60 0.060
659
P CTN015 Cutaneous T Cell Lymphoma 49 0.060
660
P MGR001 Migraine Without Aura 48 0.060
661
LYM027 Lymphopenia 57 0.060
662
GLS001 Gliosarcoma 54 0.060
663
P MRC003 Mercury Poisoning 48 0.060
664
ORG002 Organic Acidemia 43 0.060
665
CRP001 Carpal Tunnel Syndrome 67 0.060
666
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.060
667
NNT012 Neonatal Jaundice 53 0.060
668
PLC005 Placental Insufficiency 57 0.060
669
NRM005 Neuromuscular Disease 63 0.059
670
HPT022 Hepatoblastoma 56 0.059
671
CHR100 Chronic Ulcer of Skin 53 0.059
672
CND006 Candida Glabrata 32 0.059
673
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.059
674
CYT008 Cytomegalovirus Infection 56 0.059
675
NTR046 Neutrophil Migration 50 0.059
676
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.059
677
P GNT008 Giant Cell Tumor 44 0.059
678
P ICH004 Ichthyosis 54 0.059
679
HYD002 Hydronephrosis 59 0.059
680
HYP141 Hyperphenylalaninemia 38 0.059
681
P MGR003 Migraine with Aura 50 0.059
682
c MLG074 Malignant Mesenchymoma 39 0.059
683
PLS011 Plasmacytoma 56 0.058
684
IMP005 Impotence 52 0.058
685
HYP017 Hypophosphatemia 49 0.058
686
THR013 Thoracic Outlet Syndrome 53 0.058
687
P PTS002 Ptosis 52 0.058
688
c FML001 Familial Atrial Fibrillation 66 0.058
689
CRN030 Coronary Stenosis 50 0.058
690
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.058
691
P ANG015 Angioedema 54 0.058
692
c OVR114 Ovarian Cancer 1 38 0.058
693
P PLL002 Pellagra 45 0.058
694
HYP020 Hyperprolactinemia 64 0.057
695
GNR004 Generalized Anxiety Disorder 56 0.057
696
MCR017 Macrocytic Anemia 41 0.057
697
SKN019 Skin Melanoma 67 0.057
698
49X006 49, Xxxxy Syndrome 41 0.057
699
ALX003 Alexander Disease 61 0.057
700
c CHR682 Chronic Bilirubin Encephalopathy 38 0.057
701
c SPN294 Spinocerebellar Ataxia 1 52 0.057
702
P HYP111 Hyperprolinemia 39 0.057
703
PLS007 Plasmodium Falciparum Malaria 52 0.057
704
P MTC069 Mitochondrial Disorders 56 0.057
705
PRD004 Prediabetes Syndrome 47 0.057
706
AND002 Androgen Insensitivity Syndrome 66 0.056
707
BTN004 Biotin Deficiency 38 0.056
708
CNV004 Canavan Disease 60 0.056
709
TRP006 Tarp Syndrome 42 0.056
710
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 67 0.056
711
TNS005 Tonsillitis 57 0.056
712
SLC006 Silicosis 56 0.056
713
TRY001 Trypanosomiasis 50 0.056
714
EWN003 Ewing Sarcoma 68 0.056
715
CNN005 Connective Tissue Disease 66 0.056
716
GRD007 Grade Iii Astrocytoma 59 0.056
717
P ANR048 Aniridia 1 63 0.055
718
P RBL001 Rubella 58 0.055
719
CRD223 Cardiac Arrhythmia 60 0.055
720
VSC003 Visceral Leishmaniasis 55 0.055
721
SPS019 Spastic Paraparesis 40 0.055
722
WRN003 Wernicke Encephalopathy 47 0.055
723
P DRM010 Dermatomyositis 61 0.055
724
ART016 Aortic Aneurysm 68 0.055
725
SLP001 Sleeping Sickness 48 0.055
726
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.055
727
P VTR007 Vitreoretinopathy 46 0.055
728
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.054
729
c SYS043 Systemic Lupus Erythematosus 1 38 0.054
730
FCT007 Factor Vii Deficiency 66 0.054
731
P SYP003 Syphilis 59 0.054
732
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.054
733
IDP070 Idiopathic Scoliosis 37 0.054
734
P SLM003 Salmonellosis 54 0.054
735
RDC002 Radiculopathy 48 0.054
736
P NRM001 Neuromyelitis Optica 60 0.054
737
SXL003 Sexual Disorder 48 0.054
738
c VRL012 Viral Meningitis 48 0.054
739
c WLM013 Wilms Tumor 1 65 0.053
740
ATM052 Autoimmune Disease 1 37 0.053
741
P PRM002 Primary Hyperoxaluria 62 0.053
742
P EPL140 Epilepsy, Idiopathic Generalized 61 0.053
743
P NGH001 Night Blindness 47 0.053
744
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.053
745
KRT001 Keratoconjunctivitis Sicca 50 0.053
746
P CRB088 Cerebral Atrophy 38 0.053
747
ATX010 Ataxia Neuropathy Spectrum 38 0.053
748
ACT064 Acute Necrotizing Encephalitis 32 0.053
749
BLD137 Blood Group--Ahonen 19 0.053
750
SNS003 Sensory Peripheral Neuropathy 53 0.053
751
MNT001 Mantle Cell Lymphoma 66 0.053
752
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.053
753
ALL009 Allergic Conjunctivitis 50 0.052
754
ADS004 Aids Dementia Complex 40 0.052
755
RTR001 Retrograde Amnesia 45 0.052
756
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.052
757
LMB062 Limb Ischemia 55 0.052
758
P LRY044 Larynx Cancer 54 0.052
759
CHD004 Chudley-Mccullough Syndrome 44 0.052
760
P TXP001 Toxoplasmosis 60 0.052
761
HMG005 Hemoglobinopathy 55 0.052
762
MYL005 Myelofibrosis 67 0.051
763
GSG001 Gas Gangrene 50 0.051
764
HMG002 Hemoglobinuria 49 0.051
765
PLS025 Plasmablastic Lymphoma 47 0.051
766
ASP004 Asphyxia Neonatorum 45 0.051
767
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.051
768
ACR007 Acromegaly 71 0.051
769
P ANG001 Angelman Syndrome 67 0.051
770
INC002 Inclusion Body Myositis 64 0.051
771
P MMP001 Mumps 57 0.051
772
c MST023 Mesothelioma, Malignant 57 0.051
773
NRN004 Neuroendocrine Tumor 55 0.051
774
MSC190 Muscular Disease 51 0.051
775
PRN068 Paraneoplastic Limbic Encephalitis 21 0.051
776
P MYT002 Myotonic Dystrophy 49 0.050
777
PLL012 Pollen Allergy 45 0.050
778
ACT088 Acute Insulin Response 41 0.050
779
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.050
781
DFF005 Diffuse Large B-Cell Lymphoma 56 0.050
782
P MYP006 Myopia 55 0.050
783
INT067 Interstitial Nephritis 46 0.050
784
c CNG006 Congenital Hypothyroidism 65 0.050
785
P OPT009 Optic Neuritis 56 0.050
786
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.050
787
FSC002 Fascioliasis 41 0.050
788
c MLG079 Malignant Pleural Mesothelioma 42 0.050
789
P BLR006 Biliary Tract Disease 46 0.050
790
HYP835 Hypothalamic Obesity 38 0.050
791
PFF001 Pfeiffer Syndrome 79 0.050
792
MYL001 Myelitis 51 0.050
793
ANT019 Anterograde Amnesia 37 0.050
794
c BPL002 Bipolar I Disorder 49 0.050
795
MYF002 Myofascial Pain Syndrome 42 0.050
796
LST001 Listeriosis 54 0.050
797
ESP002 Esophageal Varix 51 0.050
798
ASP007 Aspiration Pneumonia 48 0.050
799
KRN002 Kearns-Sayre Syndrome 63 0.050
800
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.050
801
P INT070 Intestinal Obstruction 58 0.049
802
P CHR012 Chronic Granulomatous Disease 67 0.049
803
DCT002 Ductal Carcinoma in Situ 59 0.049
804
CLF004 Cleft Lip/palate 54 0.049
805
BRN009 Burning Mouth Syndrome 49 0.049
806
LWC001 Low Compliance Bladder 42 0.049
807
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.049
808
c PRM015 Primary Cerebellar Degeneration 36 0.049
809
OVR109 Ovarian Germ Cell Teratoma 32 0.049
810
TRT017 Teratoma, Ovarian 29 0.049
811
c JVN010 Juvenile Rheumatoid Arthritis 67 0.049
812
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 0.049
813
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.049
814
WLL004 Wallerian Degeneration 39 0.049
815
SYN036 Syncope 45 0.049
816
P MCH002 Machado-Joseph Disease 63 0.048
817
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.048
818
CYS010 Cystinosis 60 0.048
819
MCL006 Macular Retinal Edema 55 0.048
820
P FML355 Familial Intrahepatic Cholestasis 41 0.048
821
THY111 Thyroid Carcinoma, Familial Medullary 67 0.048
822
c HMP029 Hemophilia a 65 0.048
823
c PRG047 Progressive Familial Intrahepatic Cholestasis 62 0.048
824
CTN007 Cutaneous Leishmaniasis 61 0.048
825
HYP457 Hypertrophic Scars 43 0.048
826
HYP026 Hypoglycemic Coma 38 0.048
827
P KRN004 Kernicterus 47 0.048
828
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.047
829
CLR030 Clear Cell Renal Cell Carcinoma 53 0.047
830
TND006 Tendinosis 42 0.047
831
WST001 West Syndrome 60 0.047
832
RTN020 Retinal Vascular Disease 48 0.047
833
PRC013 Pericarditis 54 0.047
834
AMN001 Amenorrhea 54 0.047
835
c HPT015 Hepatitis D 49 0.047
836
VTM033 Vitamin K Deficiency Bleeding 48 0.047
837
OVR063 Overnutrition 43 0.047
838
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.047
839
VLV047 Volvulus of Midgut 50 0.047
840
CRD137 Cardiogenic Shock 48 0.047
841
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.047
842
LYM051 Lymphomatoid Granulomatosis 45 0.047
843
P HMP006 Hemiplegic Migraine 44 0.047
844
P PRV006 Pervasive Developmental Disorder 57 0.047
845
PLR007 Pleural Empyema 49 0.047
846
PRS063 Paresthesia 43 0.047
847
AMN002 Amino Acid Metabolic Disorder 40 0.047
848
c ACT004 Acute Diarrhea 39 0.046
849
KHL003 Kohlschutter-Tonz Syndrome 64 0.046
850
P MST009 Mastocytosis 63 0.046
851
P EPD016 Epidermolysis Bullosa 53 0.046
852
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.046
853
GYR004 Gyrate Atrophy of Choroid and Retina 56 0.046
854
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.046
855
c ART101 Aortic Valve Disease 2 63 0.046
856
NRL005 Neurilemmoma 60 0.046
857
PRN039 Paraneoplastic Syndromes 38 0.046
858
P CHR071 Charcot-Marie-Tooth Disease 64 0.046
859
URN010 Urinary Tract Obstruction 57 0.046
860
MYM001 Myoma 53 0.046
861
THY125 Thyroid Gland Medullary Carcinoma 51 0.046
862
TTH006 Tooth Disease 46 0.046
863
AMN012 Aminoacidopathies 21 0.046
865
CMP010 Complex Regional Pain Syndrome 58 0.045
866
URC002 Urea Cycle Disorder 51 0.045
867
P TRC031 Trichorhinophalangeal Syndrome 40 0.045
868
MTH086 Methotrexate Toxicity 33 0.045
869
INH001 Inhalation Anthrax 40 0.045
870
P GLL022 Guillain-Barre Syndrome 59 0.045
871
HYP043 Hyperandrogenism 48 0.045
872
CRN017 Coronary Thrombosis 47 0.045
873
P MTC133 Mitochondrial Myopathy 49 0.045
874
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.045
875
WLS001 Wilson Disease 70 0.045
876
PLY001 Polycythemia Vera 69 0.045
877
c NMN015 Niemann-Pick Disease, Type C1 68 0.045
878
HRP004 Herpes Zoster 60 0.045
879
GLC006 Galactosemia 65 0.045
880
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 64 0.045
881
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.045
882
BRS099 Breast Ductal Carcinoma 62 0.044
883
BRC012 Brucellosis 61 0.044
884
INT066 Interstitial Lung Disease 59 0.044
885
CLN019 Colonic Disease 46 0.044
886
c FTL006 Fetal Alcohol Spectrum Disorder 42 0.044
887
c 2HY001 2-Hydroxyglutaric Aciduria 40 0.044
888
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.044
889
c PRM108 Primary Progressive Multiple Sclerosis 51 0.044
890
SBS004 Substance Dependence 48 0.044
891
SMT001 Somatization Disorder 48 0.044
892
c HRD002 Hereditary Angioedema 61 0.044
893
ERY003 Erythema Multiforme 57 0.044
894
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.044
895
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.044
896
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.044
897
LPT001 Leptospirosis 66 0.043
898
PRT058 Pure Autonomic Failure 59 0.043
899
OPD001 Opioid Abuse 45 0.043
900
OBS003 Obsessive-Compulsive Personality Disorder 44 0.043
901
P PLY188 Polyendocrinopathy 32 0.043
902
c ALP101 Alpha-Thalassemia 62 0.043
903
IRR003 Irritant Dermatitis 47 0.043
904
ABD010 Abdominal Wall Defect 35 0.043
905
SRT004 Serotonin Syndrome 46 0.043
906
PST053 Postherpetic Neuralgia 42 0.043
907
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.043
908
DRG024 Drug Allergy 43 0.043
909
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.043
910
CMP006 Complex Partial Epilepsy 34 0.043
911
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.043
912
HMR039 Hemorrhage, Intracerebral 57 0.043
913
P ENC008 Encephalocele 47 0.043
914
FST010 Fasting Hypoglycemia 35 0.042
915
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.042
916
CRB008 Cerebral Atherosclerosis 44 0.042
917
P HRD217 Hereditary Optic Neuropathy 34 0.042
918
P RTN014 Retinal Artery Occlusion 46 0.042
919
BRN026 Branch Retinal Artery Occlusion 43 0.042
920
GLC008 Glucose Metabolism Disease 40 0.042
921
P ANT006 Antiphospholipid Syndrome 54 0.042
922
P RNV001 Renovascular Hypertension 49 0.042
923
BRN032 Brain Glioma 43 0.042
924
ART002 Arts Syndrome 63 0.042
925
ING001 Inguinal Hernia 60 0.042
926
GST037 Gastroparesis 53 0.042
927
MST020 Mast Cell Activation Syndrome 27 0.042
928
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.042
929
BNS003 Binswanger's Disease 42 0.042
930
c WLM011 Wilms Tumor 6 37 0.041
931
c RST012 Restless Legs Syndrome 1 34 0.041
932
c SCH085 Schizophrenia 2 33 0.041
933
PRR019 Perioral Myoclonia with Absences 28 0.041
934
BNG077 Benign Idiopathic Neonatal Seizures 26 0.041
935
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.041
936
MNN017 Mononeuropathy 39 0.041
937
BRN018 Borna Disease 35 0.041
938
MYF001 Myofibroma 42 0.041
939
CLF056 Cleft Lip with or Without Cleft Palate 41 0.041
940
APH002 Aphasia 57 0.041
941
CHR005 Chorioamnionitis 51 0.041
942
APR001 Apraxia 51 0.041
943
NRN001 Neuroendocrine Carcinoma 47 0.041
944
P EPS003 Episodic Ataxia 60 0.041
945
PRN032 Paraneoplastic Cerebellar Degeneration 28 0.041
946
c OPT053 Optic Atrophy 1 54 0.041
947
P PLY041 Polymyositis 57 0.041
948
CHL039 Choledocholithiasis 39 0.041
949
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.040
950
FLL027 Fallopian Tube Carcinoma 67 0.040
951
c HRD010 Hereditary Spastic Paraplegia 66 0.040
952
P ALP106 Alport Syndrome 1, X-Linked 55 0.040
953
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.040
954
c LRG001 Large Cell Carcinoma 49 0.040
955
c PRG020 Paragangliomas 3 38 0.040
956
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.040
957
INT030 Intracranial Aneurysm 56 0.040
958
OVR059 Ovary Adenocarcinoma 51 0.040
959
DVR002 Diverticulitis 44 0.040
960
CRT033 Corticobasal Degeneration 55 0.040
961
ADT003 Auditory System Disease 50 0.040
962
c HRD026 Hereditary Ataxia 48 0.040
963
CRD043 Ceroid Storage Disease 43 0.040
964
FBR012 Fabry Disease 71 0.039
965
KWS002 Kawasaki Disease 64 0.039
966
GLY010 Glycine Encephalopathy 60 0.039
967
GLL018 Gallbladder Cancer 56 0.039
968
NRG002 Neurogenic Bladder 54 0.039
969
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.039
970
P MYG005 Myoglobinuria 43 0.039
971
ENC005 Encephalomalacia 38 0.039
972
P FML187 Familial Hypertension 37 0.039
973
PRN029 Parainfluenza Virus Type 3 36 0.039
974
c CHR098 Chronic Pyelonephritis 35 0.039
975
CYN003 Cyanide Poisoning 24 0.039
976
c CNG216 Congenital Hydrocephalus 50 0.039
977
P ASP001 Asperger Syndrome 48 0.039
978
MCL003 Macular Holes 42 0.039
979
c FML023 Familial Hemiplegic Migraine 54 0.039
980
PCK003 Pick Disease of Brain 68 0.039
981
MLD001 Melioidosis 67 0.039
982
RCT015 Reactive Arthritis 60 0.039
983
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.039
984
P HYP024 Hypoparathyroidism 55 0.039
985
HML018 Homologous Wasting Disease 22 0.039
986
ONC002 Onchocerciasis 51 0.039
987
PRN009 Paranoid Schizophrenia 49 0.039
988
CRB027 Cerebellar Disease 45 0.039
989
HRN003 Heroin Dependence 44 0.039
990
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 39 0.039
991
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.039
992
CNN002 Cannabis Abuse 44 0.039
993
P CLS010 Cluster Headache 43 0.039
994
CYT004 Cytomegalic Inclusion Disease 31 0.039
995
P CHL002 Childhood Absence Epilepsy 60 0.038
996
TRG002 Trigeminal Neuralgia 60 0.038
997
TRC008 Trachoma 53 0.038
998
P SML001 Small Cell Carcinoma 52 0.038
999
IRD001 Iridocyclitis 50 0.038
1000
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.038
1001
GNT167 Genetic Obesity 34 0.038
1002
AMB001 Amebiasis 49 0.038
1003
P PRC019 Precocious Puberty 47 0.038
1004
ACT011 Acute Contagious Conjunctivitis 40 0.038
1005
c HYP597 Hyperprolinemia, Type Ii 31 0.038
1006
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.038
1007
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.038
1008
P AXN002 Axenfeld-Rieger Syndrome 58 0.038
1009
ARG007 Argininemia 57 0.038
1010
AVD001 Avoidant Personality Disorder 54 0.038
1011
PSD088 Pseudobulbar Affect 36 0.038
1012
BSL008 Basal Ganglia Disease 43 0.038
1013
MLL002 Miller Fisher Syndrome 40 0.038
1014
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.037
1015
P PTN014 Patent Ductus Arteriosus 1 60 0.037
1016
FLR002 Filariasis 55 0.037
1017
NTR018 Neutrophilia, Hereditary 52 0.037
1018
QDR001 Quadriplegia 48 0.037
1019
KLB003 Klebsiella Pneumonia 39 0.037
1020
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.037
1021
LNN001 Lennox-Gastaut Syndrome 57 0.037
1022
P HYP730 Hypogonadotropic Hypogonadism 53 0.037
1023
SCL003 Social Phobia 48 0.037
1024
P AXN001 Axonal Neuropathy 36 0.037
1025
NNS045 Non-Specific Syndromic Intellectual Disability 28 0.037
1026
c MGR030 Migraine, Familial Hemiplegic, 2 36 0.037
1027
P HYP097 Hyperekplexia 61 0.036
1028
ERY029 Erythermalgia, Primary 58 0.036
1029
TRC010 Trichotillomania 50 0.036
1030
c SCH079 Schizophrenia 1 48 0.036
1031
ANT011 Antisocial Personality Disorder 46 0.036
1032
GNT003 Genital Herpes 54 0.036
1033
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.036
1034
HND002 Hand, Foot and Mouth Disease 51 0.036
1035
SCR015 Scarlet Fever 40 0.036
1036
ORN001 Ornithosis 39 0.036
1037
ALR002 Al-Raqad Syndrome 34 0.036
1038
WBR001 Weber Syndrome 34 0.036
1039
ATH004 Athetosis 28 0.036
1040
LBR030 Leber Optic Atrophy 60 0.036
1041
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 26 0.036
1042
P MTR004 Maturity-Onset Diabetes of the Young 66 0.036
1043
ANT018 Anthracosis 48 0.036
1044
CMP034 Complete Androgen Insensitivity Syndrome 47 0.036
1045
HRD005 Hard Palate Cancer 46 0.036
1046
GST010 Gestational Trophoblastic Neoplasm 46 0.036
1047
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.036
1048
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 45 0.036
1049
TST015 Testicular Disease 43 0.036
1050
P HYP263 Hypersomnia 41 0.036
1051
GBT001 Gaba-Transaminase Deficiency 39 0.036
1052
ORN004 Ornithinemia 17 0.036
1053
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.035
1054
DMN031 Dementia, Lewy Body 65 0.035
1055
TRP002 Tropical Spastic Paraparesis 50 0.035
1056
PTH002 Pathological Gambling 48 0.035
1057
MYL057 Myelopathy, Htlv-1-Associated 39 0.035
1058
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 38 0.035
1059
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.035
1060
VRN004 Vernal Keratoconjunctivitis 47 0.035
1061
SCH011 Schizotypal Personality Disorder 39 0.035
1062
P CRB045 Cerebellar Hypoplasia 37 0.035
1063
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 22 0.035
1064
P OST001 Osteopetrosis 71 0.035
1065
LYM017 Lyme Disease 63 0.035
1066
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.035
1067
TNG003 Tongue Cancer 55 0.035
1068
PLM012 Pulmonary Sarcoidosis 53 0.035
1069
CYS014 Cystadenocarcinoma 51 0.035
1070
BLD044 Bladder Disease 48 0.035
1071
CLC006 Calcinosis 48 0.035
1072
AND014 Androgenic Alopecia 44 0.035
1073
P LYD001 Leydig Cell Tumor 43 0.035
1074
ART006 Arthus Reaction 42 0.035
1075
HPT082 Hepatic Adenomas, Familial 37 0.035
1076
HNM002 Hinman Syndrome 29 0.035
1077
ART001 Arterial Tortuosity Syndrome 66 0.034
1078
P FCL005 Focal Segmental Glomerulosclerosis 58 0.034
1079
P PNM006 Pneumoconiosis 55 0.034
1080
FND002