Search results for N(6)-(1,2-dicarboxyethyl)AMP

777 hits were found for N(6)-(1,2-dicarboxyethyl)AMP

# Family MCID Name MIFTS Score
1
P NRB001 Neuroblastoma 71 0.448
2
PRT037 Pertussis 65 0.405
3
CHL014 Cholera 55 0.387
4
HLX001 Helix Syndrome 47 0.300
5
P GLM045 Glioma 63 0.284
6
P ADN016 Adenocarcinoma 64 0.280
7
GLL048 Glial Tumor 45 0.279
8
48X005 48,xyyy 39 0.261
9
P CLR023 Colorectal Cancer 98 0.249
10
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.245
11
ISC004 Ischemia 60 0.240
12
P ENC004 Encephalitis 61 0.235
13
ADN018 Adenoma 58 0.226
14
P PHC003 Pheochromocytoma 71 0.225
15
ADR040 Adrenal Gland Pheochromocytoma 46 0.223
16
P KDN018 Kidney Disease 70 0.221
17
P BRS047 Breast Cancer 96 0.221
18
P BLD134 Bladder Cancer 78 0.219
19
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.214
20
BNR002 Bone Resorption Disease 48 0.214
21
HYP066 Hyperglycemia 61 0.213
22
P LKM002 Leukemia 66 0.212
23
FTT001 Fatty Liver Disease 61 0.212
24
P HPT023 Hepatocellular Carcinoma 100 0.203
25
P LYM031 Lymphocytic Leukemia 55 0.202
26
P LVR013 Liver Disease 68 0.201
27
P LYM118 Lymphoma 68 0.198
28
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.196
29
ALL026 Allergic Hypersensitivity Disease 64 0.194
30
P PRS040 Prostate Cancer 97 0.190
31
HMN044 Human Immunodeficiency Virus Type 1 71 0.188
32
HRW001 Hair Whorl 36 0.184
33
CYS001 Cystic Fibrosis 80 0.183
34
P LNG032 Lung Cancer 97 0.181
35
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.181
36
CYT002 Cytokine Deficiency 44 0.180
37
CNG034 Congestive Heart Failure 70 0.180
38
P OVR042 Ovarian Cancer 89 0.180
39
P HRP006 Herpes Simplex 65 0.178
40
GLB015 Glioblastoma Multiforme 75 0.178
41
P SZR006 Seizure Disorder 58 0.177
42
P MYL006 Myeloid Leukemia 60 0.175
43
ATM095 Autoimmune Disease 61 0.175
44
OST159 Osteogenic Sarcoma 66 0.175
45
VSL002 Visual Epilepsy 58 0.174
46
HYP266 Hypoxia 56 0.174
47
P ALZ034 Alzheimer Disease 88 0.174
48
HYP056 Hypoglycemia 66 0.174
49
P PNC035 Pancreatic Cancer 84 0.171
50
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.170
51
MLN008 Melanoma 69 0.168
52
P DRR001 Diarrhea 57 0.167
53
P HRT032 Heart Disease 75 0.166
54
P HYP069 Hyperparathyroidism 62 0.166
55
P AST007 Astrocytoma 50 0.165
56
P GST053 Gastric Cancer 83 0.164
57
LPD008 Lipid Metabolism Disorder 62 0.164
58
c LKM061 Leukemia, Acute Myeloid 83 0.164
59
DPR016 Depression 63 0.163
60
47X002 47,xyy 49 0.163
61
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.162
62
P RTN024 Retinoblastoma 72 0.161
63
c FML008 Familial Retinoblastoma 53 0.160
64
P PSR002 Psoriasis 62 0.159
65
PST011 Pustulosis of Palm and Sole 52 0.157
66
TTN003 Tetanus 64 0.157
67
LVR012 Liver Cirrhosis 63 0.157
68
P VSC007 Vascular Disease 63 0.157
69
P CRN018 Coronary Artery Anomaly 63 0.156
70
c HYP595 Hypertension, Essential 84 0.154
71
c HPT073 Hepatitis C Virus 70 0.154
72
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.153
73
MNT002 Mental Depression 57 0.153
74
DRM006 Dermatitis 61 0.153
75
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.153
76
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.151
77
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.149
78
STM007 Stomatitis 49 0.148
79
P MYP004 Myopathy 64 0.148
80
PNG002 Pain Agnosia 51 0.148
81
P BCL017 B-Cell Lymphoma 58 0.148
82
PPL022 Papilloma 54 0.146
83
c CHR684 Chronic Kidney Disease 66 0.146
84
AST005 Asthma 77 0.145
85
BRN071 Brain Injury 49 0.145
86
INS024 Insulin-Like Growth Factor I 79 0.144
87
LNG099 Lung Disease 61 0.143
88
c ACT071 Acute Kidney Failure 59 0.141
89
c MCR130 Microvascular Complications of Diabetes 6 41 0.141
90
P BPL003 Bipolar Disorder 56 0.140
91
P ENC018 Encephalopathy 61 0.140
92
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.139
93
MYL069 Myeloma, Multiple 85 0.138
94
c MJR024 Major Affective Disorder 9 41 0.138
95
c MJR022 Major Affective Disorder 8 38 0.138
96
P FBR017 Fibrosarcoma 56 0.138
97
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.138
98
c MCR120 Microvascular Complications of Diabetes 7 47 0.138
99
HMP009 Haemophilus Influenzae 42 0.138
100
c MCR113 Microvascular Complications of Diabetes 3 52 0.137
101
c MCR133 Microvascular Complications of Diabetes 4 41 0.137
102
P LTR001 Lateral Sclerosis 53 0.137
103
PPL052 Papillomatosis, Confluent and Reticulated 34 0.136
104
P NRP001 Neuropathy 56 0.136
105
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.135
106
CRB004 Cerebral Artery Occlusion 44 0.134
107
P HNT016 Huntington Disease 71 0.134
108
P TRT010 Teratoma 51 0.134
109
BCT022 Bacterial Infectious Disease 56 0.134
110
ANX004 Anoxia 42 0.133
111
ATH013 Atherosclerosis Susceptibility 66 0.133
112
IMM167 Immune Deficiency Disease 78 0.133
113
P MJR001 Major Depressive Disorder 68 0.132
114
BRN024 Bronchitis 68 0.132
115
SPN186 Spinal Cord Injury 60 0.132
116
c PRM005 Primary Hyperparathyroidism 58 0.132
117
P TCL004 T-Cell Leukemia 47 0.132
118
THY029 Thyroid Carcinoma 59 0.131
119
P RHN004 Rhinitis 57 0.131
120
P EXN002 Exanthem 57 0.131
121
P HYP086 Hypothyroidism 68 0.131
122
P LKM062 Leukemia, Acute Lymphoblastic 68 0.131
123
ESP021 Esophageal Cancer 90 0.131
124
c PRC016 Pre-Eclampsia 63 0.130
125
c PCH010 Pachyonychia Congenita 3 43 0.130
126
VCC001 Vaccinia 49 0.130
127
END030 End Stage Renal Failure 58 0.130
128
P PLM037 Pulmonary Hypertension 68 0.129
129
CHL123 Chlamydia 59 0.129
130
c SYS001 Systemic Lupus Erythematosus 86 0.128
131
P INF037 Inflammatory Bowel Disease 56 0.128
132
SQM006 Squamous Cell Carcinoma 60 0.128
133
c SML038 Small Cell Cancer of the Lung 65 0.127
134
c ACT075 Acute Myocardial Infarction 56 0.127
135
c HYP836 Hypercholesterolemia, Familial, 1 72 0.126
136
TRM010 Traumatic Brain Injury 53 0.126
137
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.126
138
P CHR345 Chronic Pain 50 0.125
139
P MSC005 Muscular Dystrophy 66 0.125
140
CHR074 Choriocarcinoma 46 0.125
141
c SVR001 Severe Acute Respiratory Syndrome 55 0.125
142
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.124
143
ALC007 Alcohol Dependence 66 0.124
144
P HPT021 Hepatitis 67 0.123
145
P TRM003 Tremor 53 0.123
146
LSH001 Leishmaniasis 63 0.123
147
P KLZ004 Kala-Azar 1 41 0.123
148
ALL003 Allergic Rhinitis 67 0.122
149
SVR004 Severe Combined Immunodeficiency 73 0.122
150
TXC005 Toxic Shock Syndrome 61 0.122
151
MSL001 Measles 61 0.121
152
c ATR087 Atrial Standstill 1 74 0.121
153
OCL069 Ocular Motor Apraxia 51 0.121
154
P DRM053 Dermatitis, Atopic 66 0.121
155
P NTR004 Neutropenia 63 0.121
156
PTT037 Pituitary Tumors 44 0.120
157
P DBT009 Diabetes Mellitus 64 0.120
158
P ATX030 Ataxia-Telangiectasia 83 0.120
159
c ACT073 Acute Leukemia 58 0.119
160
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.119
161
c HPT001 Hepatitis C 63 0.119
162
CHR178 Chromosomal Triplication 35 0.119
163
P INF038 Influenza 68 0.118
164
DPH001 Diphtheria 60 0.118
165
OST012 Osteoarthritis 78 0.118
166
P MCR115 Microvascular Complications of Diabetes 5 66 0.117
167
DWN001 Down Syndrome 70 0.117
168
P HYP076 Hyperthyroidism 55 0.117
169
P PLM036 Pulmonary Fibrosis 61 0.117
170
c HPT016 Hepatitis B 59 0.116
171
IDP011 Idiopathic Interstitial Pneumonia 63 0.116
172
P RTN016 Retinal Degeneration 53 0.116
173
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.116
174
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.115
175
HYP060 Hyperinsulinism 54 0.115
176
c MGR028 Migraine with or Without Aura 1 69 0.115
177
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.115
178
PST092 Posttransplant Acute Limbic Encephalitis 29 0.114
180
P CRN300 Coronary Heart Disease 1 63 0.114
181
P PLY014 Polycystic Kidney Disease 59 0.114
182
P SCH015 Schizophrenia 75 0.114
183
TRT001 Teratocarcinoma 46 0.113
184
GLC003 Glucose Intolerance 54 0.113
185
ART140 Arteries, Anomalies of 53 0.113
186
ACQ007 Acquired Immunodeficiency Syndrome 60 0.113
187
P ATS364 Autism 65 0.113
188
ADL002 Adult Syndrome 69 0.112
189
P RHM011 Rheumatoid Arthritis 80 0.111
190
P PLY011 Polycystic Ovary Syndrome 56 0.111
191
ALL014 Allergic Encephalomyelitis 39 0.111
192
P CTR002 Cataract 60 0.110
193
GST045 Gastroenteritis 59 0.110
194
MST004 Mast Cell Neoplasm 38 0.109
195
EXT007 Extracutaneous Mastocytoma 38 0.109
196
CRV035 Cervical Cancer 76 0.109
197
MYL009 Myelodysplastic Syndrome 70 0.109
198
P MNN013 Meningitis 65 0.108
199
EMB004 Embryonal Carcinoma 57 0.108
200
CRB039 Cerebrovascular Disease 69 0.108
201
ANX010 Anxiety 72 0.108
202
P OST002 Osteoporosis 73 0.107
203
P PRP019 Peripheral Nervous System Disease 57 0.107
204
P LNG064 Lung Cancer Susceptibility 3 77 0.107
205
AGN016 Aging 56 0.106
206
CHL068 Cholestasis 60 0.106
207
P RHB003 Rhabdomyosarcoma 62 0.106
208
INS001 Insulinoma 60 0.106
209
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.105
210
RCK004 Rickets 69 0.104
211
P MSC003 Muscular Atrophy 52 0.104
212
c RHB024 Rhabdomyosarcoma 2 65 0.103
213
STT001 Status Epilepticus 59 0.103
214
P MYC007 Myocardial Infarction 70 0.102
215
SPN035 Spindle Cell Sarcoma 51 0.102
216
DFC004 Deficiency Anemia 75 0.102
217
P PRD008 Periodontitis 62 0.102
218
P HYP061 Hypertrophic Cardiomyopathy 66 0.102
219
PLM001 Pulmonary Tuberculosis 70 0.102
220
P HDC001 Headache 57 0.101
221
PLY150 Polykaryocytosis Inducer 31 0.101
222
P CRD246 Cardiovascular System Disease 56 0.101
223
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.101
224
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.101
225
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.101
226
SRC014 Sarcoma 65 0.100
227
ATS010 Autosomal Recessive Disease 48 0.100
228
P LPS004 Lupus Erythematosus 61 0.100
229
SKN016 Skin Disease 63 0.100
230
P INF032 Infertility 57 0.100
231
c ACT027 Acute Pancreatitis 59 0.099
232
CLT003 Colitis 62 0.099
233
P PNM007 Pneumonia 68 0.099
234
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.099
235
P MLT020 Multiple Sclerosis 72 0.099
236
ERY051 Erythroleukemia, Familial 56 0.098
237
P ALC033 Alcohol Use Disorder 58 0.098
238
CLN015 Colon Adenocarcinoma 63 0.098
239
P GST044 Gastritis 55 0.098
240
ANG054 Angina Pectoris 66 0.097
241
c DLT002 Dilated Cardiomyopathy 79 0.097
242
P TRC086 Trichohepatoenteric Syndrome 1 59 0.097
243
P THR014 Thrombocytopenia 68 0.097
244
GST040 Gastric Adenocarcinoma 70 0.096
245
TLN003 Telangiectasis 51 0.096
246
P PRK057 Parkinson Disease, Late-Onset 76 0.096
247
CNT047 Contact Dermatitis 57 0.096
248
CLF027 Cleft Palate, Isolated 64 0.095
249
c ACT134 Acute Liver Failure 51 0.095
250
P RSP003 Respiratory Failure 74 0.095
251
LYM019 Lymphosarcoma 47 0.095
252
TRN018 Transitional Cell Carcinoma 56 0.094
253
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.094
254
P GLM040 Glioma Susceptibility 1 81 0.093
255
P HYP098 Hypereosinophilic Syndrome 66 0.093
256
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.093
257
CHG001 Chagas Disease 66 0.093
258
PLM010 Pulmonary Edema 55 0.092
259
END057 Endometrial Cancer 74 0.092
260
P CRD119 Cardiac Arrest 67 0.092
261
c MLG068 Malignant Glioma 45 0.092
262
IMP005 Impotence 52 0.092
263
CRH001 Crohn's Disease 74 0.092
264
P KDN017 Kidney Cancer 61 0.092
265
P GRV001 Graves' Disease 55 0.092
266
P MJR007 Major Affective Disorder 1 43 0.092
267
THR013 Thoracic Outlet Syndrome 53 0.091
268
IRN002 Iron Metabolism Disease 57 0.091
269
P CND004 Candidiasis 57 0.091
270
c ATS007 Autism Spectrum Disorder 67 0.090
271
CHL079 Children's Interstitial Lung Disease 27 0.090
272
c HPT003 Hepatitis a 63 0.089
273
c LKM063 Leukemia, Chronic Myeloid 71 0.089
274
NNL006 Non-Alcoholic Steatohepatitis 51 0.089
275
P TBR001 Tuberous Sclerosis 70 0.089
276
P BND020 Bone Disease 59 0.088
277
P MDL005 Medulloblastoma 77 0.088
278
c ACT068 Acute Cystitis 63 0.088
279
P ECL001 Eclampsia 51 0.088
280
P MYC008 Myocarditis 59 0.088
281
P PNC044 Pancreatitis 61 0.088
282
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.088
283
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.087
284
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.086
285
ORL011 Oral Cancer 60 0.086
286
P ART022 Arthritis 70 0.086
287
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.086
288
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.086
289
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.086
290
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.086
291
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.086
292
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.086
293
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.086
294
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.086
295
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.086
296
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.086
297
P END044 Endometriosis 62 0.086
298
c SCL052 Scleroderma, Familial Progressive 62 0.085
299
P GRF003 Graft-Versus-Host Disease 71 0.085
300
MSC007 Muscle Hypertrophy 63 0.085
301
P EPL164 Epilepsy 71 0.085
302
P HYP750 Hypertriglyceridemia, Familial 61 0.085
303
ARG004 Argyria 28 0.084
304
MTB004 Metabolic Acidosis 50 0.084
305
ALL006 Allergic Asthma 56 0.084
306
ANR040 Aneurysm 58 0.084
307
CHC001 Chickenpox 60 0.084
308
P BNG032 Benign Mesothelioma 45 0.084
309
P MYT002 Myotonic Dystrophy 49 0.084
310
STR067 Stroke, Ischemic 80 0.084
311
MDD011 Mood Disorder 62 0.083
312
c PNS012 Paine Syndrome 61 0.083
313
P FRG001 Fragile X Syndrome 68 0.083
314
P ATR011 Atrial Fibrillation 66 0.083
315
RNL077 Renal Fibrosis 47 0.083
316
P DYS154 Dystonia 65 0.083
317
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.083
318
P HML002 Hemolytic Anemia 62 0.083
319
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.082
320
ART016 Aortic Aneurysm 68 0.082
321
P SKN015 Skin Carcinoma 67 0.082
322
GT001 Gout 63 0.082
323
P HYP265 Hypotonia 42 0.082
324
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.082
325
MLR004 Malaria 80 0.082
326
NTR005 Nutritional Deficiency Disease 61 0.082
327
INT007 Intermediate Coronary Syndrome 55 0.082
328
c LKM071 Leukemia, Chronic Lymphocytic 79 0.082
329
SPL018 Splenomegaly 48 0.081
330
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.081
331
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.081
332
HDN002 Head Injury 45 0.081
333
KPS004 Kaposi Sarcoma 75 0.081
334
VRL011 Viral Infectious Disease 61 0.081
335
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.081
336
LYM133 Lymphoma, Hodgkin, Classic 69 0.080
337
AND002 Androgen Insensitivity Syndrome 66 0.080
338
DNT012 Dental Caries 51 0.080
339
EWN003 Ewing Sarcoma 68 0.080
340
IGR001 Ige Responsiveness, Atopic 59 0.080
341
AMN003 Amnestic Disorder 54 0.080
342
SPP010 Suppressor of Tumorigenicity 3 51 0.080
343
ORL015 Oral Squamous Cell Carcinoma 43 0.079
344
c SCN007 Secondary Hyperparathyroidism 50 0.079
345
CHL065 Cholangiocarcinoma 67 0.079
346
P MYC084 Mycobacterium Tuberculosis 1 68 0.079
347
P DMN002 Dementia 67 0.079
348
GTR002 Goiter 52 0.079
349
P NPH012 Nephrotic Syndrome 63 0.079
350
P SRC025 Sarcoidosis 1 70 0.078
351
END040 Endogenous Depression 54 0.078
352
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.078
353
SKN019 Skin Melanoma 67 0.078
354
PPT005 Peptic Ulcer Disease 58 0.078
355
c ADL017 Adult T-Cell Leukemia 57 0.078
356
INT079 Intrahepatic Cholangiocarcinoma 50 0.078
357
GST023 Gastric Ulcer 53 0.078
358
P VSC011 Vasculitis 62 0.078
359
P NRF023 Neurofibromatosis, Type Ii 76 0.077
360
ANT024 Anthrax Disease 58 0.077
361
P SYS005 Systemic Scleroderma 70 0.077
362
P HYD006 Hydrocephalus 65 0.077
363
c TBR025 Tuberous Sclerosis 1 76 0.077
364
P PYL005 Pyelonephritis 56 0.077
365
MST005 Mastitis 53 0.076
366
P SLP006 Sleep Apnea 69 0.076
367
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.076
368
P END033 Endocarditis 57 0.076
369
BRN002 Bronchiolitis 59 0.076
370
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.076
371
HYP005 Hypokalemia 55 0.076
372
P AXN002 Axenfeld-Rieger Syndrome 58 0.076
373
NTR046 Neutrophil Migration 50 0.075
374
P DDN001 Duodenal Ulcer 50 0.075
375
PLG002 Plague 57 0.075
376
BRR014 Barrett Esophagus 64 0.075
377
c BRN108 Branchiootic Syndrome 1 61 0.074
378
ALR002 Al-Raqad Syndrome 34 0.074
379
P CYS018 Cystitis 59 0.074
380
OTT002 Otitis Media 71 0.074
381
MCR013 Microphthalmia 60 0.073
382
P MYC033 Myoclonus 46 0.073
383
P DBT005 Diabetes Insipidus 55 0.073
384
BRN004 Brain Edema 55 0.073
385
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.073
386
PNC129 Pancreatic Adenocarcinoma 67 0.073
387
SLC006 Silicosis 56 0.073
388
PLS011 Plasmacytoma 56 0.072
389
CRB037 Cerebral Palsy 68 0.072
390
P GCH001 Gaucher's Disease 64 0.072
391
HMS001 Hemosiderosis 54 0.072
392
P PSD015 Pseudohypoparathyroidism 56 0.072
393
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.072
394
ACR006 Aceruloplasminemia 73 0.072
395
WTH001 Withdrawal Disorder 48 0.071
396
TRN015 Transient Cerebral Ischemia 62 0.071
397
DFF005 Diffuse Large B-Cell Lymphoma 56 0.071
398
HPT004 Hepatic Coma 43 0.071
399
CRD137 Cardiogenic Shock 48 0.071
400
URM002 Uremia 49 0.071
401
P MLN007 Male Infertility 56 0.070
402
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.070
403
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.070
404
DSS008 Disease of Mental Health 57 0.070
405
c FNC043 Fanconi Anemia, Complementation Group E 62 0.070
406
P HMN010 Hemangioma 61 0.070
407
P RRH023 Rare Hereditary Hemochromatosis 41 0.070
408
KWS002 Kawasaki Disease 64 0.070
409
P PRS038 Personality Disorder 65 0.069
410
P SCK005 Sickle Cell Disease 50 0.069
411
P ALP008 Alopecia 56 0.069
412
DMY004 Demyelinating Disease 52 0.069
413
c THR092 Thrombophilia Due to Thrombin Defect 73 0.069
414
TRY001 Trypanosomiasis 50 0.069
415
VSC003 Visceral Leishmaniasis 55 0.069
416
P MYS003 Myasthenia Gravis 68 0.069
417
BCK006 Back Pain 42 0.069
418
P RBL001 Rubella 58 0.068
419
P DNG005 Dengue Virus 57 0.068
420
CYT008 Cytomegalovirus Infection 56 0.068
421
c VRL010 Viral Hepatitis 51 0.068
422
CRD223 Cardiac Arrhythmia 60 0.068
423
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.068
424
P SML001 Small Cell Carcinoma 52 0.068
425
P OPN001 Open-Angle Glaucoma 49 0.068
426
P THY023 Thymoma 65 0.068
427
c THY107 Thymoma, Familial 54 0.068
428
ACT119 Acute Promyelocytic Leukemia 63 0.067
429
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.067
430
P CNR004 Cone-Rod Dystrophy 2 71 0.067
431
URT010 Ureteral Obstruction 46 0.067
432
P HYP024 Hypoparathyroidism 55 0.067
433
P OBS001 Obstructive Jaundice 48 0.067
434
c MNN043 Meningioma, Familial 74 0.066
435
MNN042 Meningioma, Radiation-Induced 62 0.066
436
SPN021 Spinal Meningioma 47 0.066
437
TBC004 Tobacco Addiction 64 0.066
438
MSC157 Muscular Dystrophy, Duchenne Type 71 0.066
439
CRC021 Carcinosarcoma 61 0.066
440
NRL016 Neural Tube Defects 82 0.066
441
P GLY013 Glycogen Storage Disease 59 0.066
442
c MJR003 Major Affective Disorder 6 33 0.066
443
c DWL002 Dowling-Degos Disease 1 58 0.066
444
SCR001 Secretory Meningioma 37 0.066
445
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.066
446
CCN002 Cocaine Abuse 48 0.066
447
IGG001 Iga Glomerulonephritis 48 0.065
448
c GCH015 Gaucher Disease, Type I 70 0.065
449
P LKD001 Leukodystrophy 59 0.065
450
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.065
451
P MTR014 Motor Neuron Disease 64 0.065
452
NRT001 Neurotic Disorder 52 0.065
453
P VTR007 Vitreoretinopathy 46 0.064
454
MNN009 Meningoencephalitis 49 0.064
455
KRT019 Keratitis, Hereditary 67 0.064
456
LMY002 Leiomyoma 50 0.064
457
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.064
458
CRD132 Cardiac Conduction Defect 59 0.064
459
P SYP003 Syphilis 59 0.064
460
c MJR006 Major Affective Disorder 5 33 0.063
461
P MNC007 Monocytic Leukemia 54 0.063
462
SYN036 Syncope 45 0.063
463
CTN007 Cutaneous Leishmaniasis 61 0.063
464
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.063
465
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.062
466
P CHN012 Chondrosarcoma 56 0.062
467
P ADL010 Adult Respiratory Distress Syndrome 63 0.062
468
NRM005 Neuromuscular Disease 63 0.062
469
SCK003 Sickle Cell Anemia 72 0.061
470
PLR008 Pleurisy 51 0.061
471
CRT015 Carotid Artery Occlusion 44 0.061
472
DBT010 Diabetic Neuropathy 55 0.061
473
HPT019 Hepatic Encephalopathy 60 0.061
474
OST003 Osteonecrosis 61 0.061
475
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.061
476
END041 Endometrial Adenocarcinoma 63 0.061
477
PST028 Post-Traumatic Stress Disorder 58 0.060
478
HYP080 Hypogonadism 50 0.060
479
ANG005 Anogenital Venereal Wart 56 0.060
480
P LNG028 Long Qt Syndrome 65 0.060
481
P LCT001 Lactic Acidosis 51 0.060
482
IRR002 Irritable Bowel Syndrome 63 0.060
483
GST033 Gestational Diabetes 57 0.060
484
c PRS136 Prostate Cancer, Hereditary, 6 33 0.059
485
THY128 Thyroid Tumor 47 0.059
486
BRC012 Brucellosis 61 0.059
487
LMB062 Limb Ischemia 55 0.059
488
HYP064 Hypogonadotropism 40 0.059
489
c PRG020 Paragangliomas 3 38 0.059
490
BLR008 Bilirubin Metabolic Disorder 57 0.059
491
P PRP029 Porphyria 62 0.059
492
c BSL007 Basal Cell Carcinoma 68 0.059
493
NRL005 Neurilemmoma 60 0.059
494
P SPN046 Spinal Muscular Atrophy 64 0.058
495
ACT084 Acute Stress Disorder 48 0.058
496
c MJR008 Major Affective Disorder 2 34 0.058
497
c MJR023 Major Affective Disorder 7 33 0.058
498
c MJR004 Major Affective Disorder 4 28 0.058
499
DYS015 Dysentery 50 0.058
500
c MST023 Mesothelioma, Malignant 57 0.058
501
HRP004 Herpes Zoster 60 0.058
502
NRF007 Neurofibroma 64 0.058
503
ADR007 Adrenoleukodystrophy 74 0.058
504
LYM027 Lymphopenia 57 0.057
505
P MTR004 Maturity-Onset Diabetes of the Young 66 0.057
506
P ESP024 Esophagitis 62 0.057
507
P NRV007 Nervous System Disease 66 0.057
508
LYM017 Lyme Disease 63 0.057
509
TYP007 Typhoid Fever 63 0.057
510
c GLL024 Gallbladder Disease 1 52 0.057
511
c PRS130 Prostate Cancer, Hereditary, 8 32 0.057
512
THY111 Thyroid Carcinoma, Familial Medullary 67 0.057
513
DYS073 Dysphagia 50 0.057
514
CHR005 Chorioamnionitis 51 0.057
515
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.056
516
THY125 Thyroid Gland Medullary Carcinoma 51 0.056
517
ETN001 Eating Disorder 59 0.056
518
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.056
519
c GLC092 Glaucoma, Primary Open Angle 62 0.056
520
ATR057 Atrioventricular Block 55 0.056
521
P ART021 Arteriosclerosis 54 0.056
522
ALC006 Alcoholic Hepatitis 61 0.056
523
P PRM006 Primary Biliary Cirrhosis 61 0.055
524
c FNC027 Fanconi Anemia, Complementation Group a 81 0.055
525
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.055
526
MYL031 Myeloproliferative Neoplasm 65 0.055
527
P PNC025 Panic Disorder 53 0.055
528
P RTT002 Rett Syndrome 80 0.055
529
ADR022 Adrenomyeloneuropathy 38 0.055
530
P MYS079 Miyoshi Muscular Dystrophy 53 0.054
531
PLL012 Pollen Allergy 45 0.054
532
PLS009 Plasma Cell Neoplasm 51 0.054
533
P THY032 Thyroiditis 53 0.054
534
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.054
535
MSC190 Muscular Disease 51 0.054
536
c GRV008 Graves Disease 1 55 0.053
537
c PRD040 Periodontitis, Chronic 54 0.053
538
HRT012 Heart Valve Disease 53 0.053
539
OVR063 Overnutrition 43 0.053
540
GST050 Gastrointestinal System Disease 56 0.053
541
P RNL015 Renal Hypertension 48 0.053
542
P MTH007 Methemoglobinemia 46 0.053
543
P PRV006 Pervasive Developmental Disorder 57 0.053
544
MYL005 Myelofibrosis 67 0.053
545
HRN029 Hearing Loss, Noise-Induced 37 0.053
546
P ACR001 Aicardi-Goutieres Syndrome 65 0.053
547
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.053
548
GRW007 Growth Hormone Deficiency 43 0.053
549
c LKM070 Leukemia, Acute Monocytic 53 0.053
550
P MTC069 Mitochondrial Disorders 56 0.053
551
WLL004 Wallerian Degeneration 39 0.053
552
OCL052 Ocular Dominance 41 0.052
553
P MYC026 Myoclonus Epilepsy 35 0.052
554
c CNT035 Central Nervous System Disease 54 0.052
555
MYC019 Mycobacterium Marinum 29 0.052
556
P CYS039 Cystic Kidney Disease 54 0.052
557
VLV047 Volvulus of Midgut 50 0.052
558
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.052
559
NRT004 Neuritis 53 0.052
560
LKP003 Leukoplakia 39 0.052
561
P INT068 Intestinal Disease 52 0.052
562
P CHL066 Cholangitis 50 0.052
563
ADR016 Adrenal Cortical Carcinoma 48 0.051
564
P PLY041 Polymyositis 57 0.051
565
HRP009 Herpes Simplex Encephalitis 50 0.051
566
PPL002 Papillary Carcinoma 47 0.051
567
CRH005 Crohn's Colitis 52 0.051
568
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.051
569
PHN003 Phenylketonuria 75 0.051
570
ACR007 Acromegaly 71 0.051
571
PTZ001 Peutz-Jeghers Syndrome 69 0.051
572
TXC002 Toxic Encephalopathy 52 0.051
573
STN013 Stenotrophomonas Maltophilia Infection 25 0.051
575
c HMC039 Hemochromatosis, Type 1 74 0.051
576
RFR010 Refractory Anemia 48 0.050
577
SFT003 Soft Tissue Sarcoma 56 0.050
578
ALB002 Albinism 46 0.050
579
ADR004 Adrenal Cortical Adenocarcinoma 38 0.050
580
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.050
581
P MMP001 Mumps 57 0.050
582
P PTT006 Pituitary Adenoma 54 0.050
583
P OLG002 Oligodendroglioma 67 0.050
584
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.050
585
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.050
586
P PRC019 Precocious Puberty 47 0.049
587
P HMR003 Hemorrhagic Disease 52 0.049
588
CRV040 Cervix Carcinoma 50 0.049
589
PFF001 Pfeiffer Syndrome 79 0.049
590
P CHR012 Chronic Granulomatous Disease 67 0.049
591
SCH012 Schizoaffective Disorder 50 0.049
592
BLD131 Bladder Urothelial Carcinoma 61 0.049
593
TRD006 Tardive Dyskinesia 55 0.049
594
BRN012 Bronchiolitis Obliterans 56 0.049
595
P END046 Endometritis 47 0.049
596
P RRT020 Rare Tumor 41 0.048
597
PST021 Postpartum Depression 50 0.048
598
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.048
599
HYP014 Hyperuricemia 51 0.048
600
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.047
601
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.047
602
MMM001 Mammary Paget's Disease 53 0.047
603
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.047
604
ASP003 Aseptic Meningitis 51 0.047
605
P CHR071 Charcot-Marie-Tooth Disease 64 0.047
606
INF034 Infective Endocarditis 52 0.047
607
THY030 Thyroid Gland Disease 51 0.047
608
GRM010 Germ Cells Tumors 34 0.047
609
CRY005 Cryptococcosis 58 0.047
610
OPD006 Opioid Addiction 48 0.047
611
GNG002 Ganglioneuroma 53 0.047
612
c ATM011 Autoimmune Hepatitis 62 0.047
613
P ANT006 Antiphospholipid Syndrome 54 0.047
614
WST005 West Nile Virus 55 0.046
615
ACT200 Acute Monoblastic Leukemia 55 0.046
616
c PRG011 Progressive Myoclonus Epilepsy 42 0.046
617
CLC006 Calcinosis 48 0.046
618
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.045
619
c ACT020 Acute T Cell Leukemia 53 0.045
620
c VRL007 Viral Encephalitis 51 0.045
621
P PMP001 Pemphigus 55 0.045
622
P MYG005 Myoglobinuria 43 0.044
623
CYS010 Cystinosis 60 0.044
624
c ACT042 Acute Pyelonephritis 44 0.044
625
P END047 Endophthalmitis 52 0.044
626
P VNW001 Von Willebrand's Disease 64 0.044
627
c ART101 Aortic Valve Disease 2 63 0.044
628
ART002 Arts Syndrome 63 0.044
629
P CHR285 Chronic Myelomonocytic Leukemia 59 0.044
630
P FTL001 Fetal Alcohol Syndrome 55 0.044
631
GNG005 Gangliocytoma 55 0.043
632
QDR001 Quadriplegia 48 0.043
633
RYN005 Raynaud Phenomenon 46 0.043
634
MYM001 Myoma 53 0.043
635
P OCL002 Oculocutaneous Albinism 60 0.043
636
TNS005 Tonsillitis 57 0.043
637
PNC001 Pancytopenia 54 0.043
638
TTH006 Tooth Disease 46 0.043
639
P MLN069 Melanoma, Uveal 58 0.043
640
P TST021 Testicular Germ Cell Tumor 61 0.043
641
c SPN393 Spinal Muscular Atrophy, Type I 53 0.042
642
P INT143 Interstitial Cystitis 61 0.042
643
P BNG030 Benign Ependymoma 60 0.042
644
P MLT074 Multiple Endocrine Neoplasia 55 0.042
645
CLL010 Cellular Ependymoma 53 0.042
646
P BLD062 Bile Duct Cancer 65 0.042
647
ORL012 Oral Leukoplakia 39 0.042
648
WHP002 Whiplash 36 0.042
649
BLM002 Bulimia Nervosa 57 0.042
650
NPH003 Nephrocalcinosis 51 0.042
651
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.042
652
c SVR005 Severe Pre-Eclampsia 49 0.042
653
P CRB059 Cerebellar Degeneration 37 0.042
654
CNN003 Conn's Syndrome 79 0.042
655
HPT014 Hepatorenal Syndrome 50 0.042
656
BRS051 Breast Disease 58 0.042
657
CCC001 Coccidioidomycosis 53 0.042
658
OPT003 Opiate Dependence 50 0.041
659
P LCH002 Lichen Planus 54 0.041
660
PLV003 Pelvic Inflammatory Disease 55 0.041
661
MYT011 Myotonia 35 0.041
662
ADN022 Adenylosuccinase Deficiency 43 0.041
663
c BCT013 Bacterial Pneumonia 47 0.041
664
PLC008 Placenta Disease 49 0.041
665
P PGT001 Paget's Disease of Bone 60 0.041
666
FBR009 Fibrous Dysplasia 48 0.041
667
PCK003 Pick Disease of Brain 68 0.040
668
P RNL007 Renal Tubular Acidosis 50 0.040
669
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.040
670
ECH003 Echinococcosis 53 0.040
671
SXL003 Sexual Disorder 48 0.040
672
c MLG079 Malignant Pleural Mesothelioma 42 0.040
673
c NRF024 Neurofibromatosis, Type I 71 0.039
674
PHR003 Pharyngitis 56 0.039
675
MTC005 Mitochondrial Metabolism Disease 48 0.039
676
GSG001 Gas Gangrene 50 0.039
677
APR001 Apraxia 51 0.039
678
RSP021 Respiratory Allergy 45 0.039
679
DCB001 Decubitus Ulcer 60 0.039
680
SPN050 Spinocerebellar Degeneration 41 0.039
681
P KRB001 Krabbe Disease 69 0.039
682
P OST001 Osteopetrosis 71 0.038
683
MGK001 Megakaryocytic Leukemia 64 0.038
684
c ATM022 Autoimmune Myocarditis 35 0.038
685
P ALP009 Alopecia Areata 60 0.038
686
LMY014 Leiomyoma, Uterine 56 0.038
687
P GNT008 Giant Cell Tumor 44 0.038
688
c CNG006 Congenital Hypothyroidism 65 0.038
689
ENT001 Enterocele 39 0.038
690
P BRC006 Brachydactyly 53 0.038
691
P TST026 Testicular Germ Cell Cancer 44 0.037
692
P AGM001 Agammaglobulinemia 65 0.037
693
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.037
694
OST011 Osteomalacia 52 0.037
695
P AGG001 Aggressive Periodontitis 50 0.037
696
P HYP730 Hypogonadotropic Hypogonadism 53 0.037
697
MYF002 Myofascial Pain Syndrome 42 0.037
698
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.037
699
APH001 Aphthous Stomatitis 57 0.036
700
P CLL015 Collagen Disease 42 0.036
701
BLM001 Bloom Syndrome 66 0.036
702
c TBR026 Tuberous Sclerosis 2 71 0.036
703
P PLV020 Pelvic Organ Prolapse 59 0.036
704
P MLG056 Malignant Hyperthermia 67 0.036
705
PRT029 Parathyroid Adenoma 50 0.036
706
PRT018 Portal Vein Thrombosis 50 0.036
707
P PRD021 Periodic Paralysis 46 0.036
708
c CHR064 Chronic Monocytic Leukemia 34 0.036
709
ASB001 Asbestosis 46 0.035
710
ASB003 Asbestos Intoxication 26 0.035
711
PRD004 Prediabetes Syndrome 47 0.035
712
OBS082 Obstructive Nephropathy 43 0.035
714
DST006 Diastolic Heart Failure 44 0.035
715
P FNC004 Fanconi Syndrome 50 0.035
716
P FML187 Familial Hypertension 37 0.035
717
P PNT019 Pontocerebellar Hypoplasia 46 0.035
718
MST024 Mastocytosis, Cutaneous 67 0.034
719
QFV001 Q Fever 58 0.034
720
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.034
721
PLY023 Polycystic Liver Disease 57 0.034
722
SBS004 Substance Dependence 48 0.034
723
HYP141 Hyperphenylalaninemia 38 0.034
724
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.034
725
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.034
726
ISL001 Islet Cell Tumor 56 0.033
727
MCR018 Microcytic Anemia 47 0.033
728
GNT003 Genital Herpes 54 0.033
729
OCL022 Ocular Melanoma 53 0.033
730
ASP007 Aspiration Pneumonia 48 0.033
731
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.032
732
ADR005 Adrenal Carcinoma 58 0.032
733
SPN041 Spinal Cord Disease 56 0.032
734
LSS003 Lassa Fever 48 0.032
735
P CRV031 Cervical Adenocarcinoma 47 0.032
736
CNG028 Congenital Hypoplastic Anemia 46 0.032
737
MLN003 Melancholia 39 0.032
738
IDP091 Idiopathic Nephrotic Syndrome 38 0.032
739
HGH001 High Pressure Neurological Syndrome 24 0.032
740
BCL014 B-Cell Growth Factor 34 0.032
741
P PTT014 Pitt-Hopkins Syndrome 60 0.032
742
RSC001 Rosacea 55 0.032
743
P EMB005 Embryonal Rhabdomyosarcoma 53 0.032
744
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.032
745
TRP005 Trophoblastic Neoplasm 38 0.032
746
c HNT011 Huntington Disease-Like 3 38 0.032
747
P OLV001 Olivopontocerebellar Atrophy 52 0.031
748
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.031
749
c LNG047 Long Qt Syndrome 2 58 0.030
750
CHR100 Chronic Ulcer of Skin 53 0.030
751
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 50 0.030
752
CRY014 Cryptococcal Meningitis 48 0.030
753
c PRG106 Progressive Muscular Dystrophy 33 0.030
754
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.030
755
P WRD001 Waardenburg's Syndrome 59 0.030
756
SCN001 Secondary Hyperparathyroidism of Renal Origin 28 0.030
757
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.029
758
c GST103 Gastric Cancer, Hereditary Diffuse 64 0.029
759
HRL003 Hurler Syndrome 59 0.029
760
HYP025 Hyperphosphatemia 47 0.029
761
CHD001 Chediak-Higashi Syndrome 66 0.028
762
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.028
763
CLN019 Colonic Disease 46 0.028
764
P LPM005 Lipomatosis 45 0.028
765
BCT021 Bacterial Sepsis 44 0.028
766
AML001 Amelanotic Melanoma 39 0.028
767
P SCL048 Sclerosteosis 53 0.027
768
P HYP776 Hyperparathyroidism, Neonatal Severe 47 0.027
769
ISC015 Ischemic Colitis 44 0.027
770
P DFF019 Diffuse Gastric Cancer 43 0.027
771
SCR003 Secretory Diarrhea 36 0.027
773
FBR086 Fibrolamellar Carcinoma 59 0.026
774
CRN017 Coronary Thrombosis 47 0.026
775
HMM004 Hamamy Syndrome 37 0.026
776
CRY036 Cryptogenic Cirrhosis 36 0.026
777
OST006 Osteoblastoma 35 0.026
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