Search results for Adenosine monophosphate

686 hits were found for Adenosine monophosphate

# Family MCID Name MIFTS Score
1
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 7.604
2
ERY039 Erythrocyte Amp Deaminase Deficiency 21 3.107
3
CHL014 Cholera 59 0.471
4
PRT037 Pertussis 65 0.426
5
P NRB001 Neuroblastoma 72 0.301
6
ADN001 Adenosine Deaminase Deficiency 47 0.269
7
HYP266 Hypoxia 57 0.249
8
ISC004 Ischemia 58 0.249
9
IMM167 Immune Deficiency Disease 78 0.218
10
GLL048 Glial Tumor 45 0.208
11
P GLM045 Glioma 63 0.206
12
P HYP069 Hyperparathyroidism 63 0.190
13
CNG034 Congestive Heart Failure 69 0.185
14
48X005 48,xyyy 39 0.183
15
P LKM002 Leukemia 68 0.179
16
ANX004 Anoxia 40 0.176
17
P PHC003 Pheochromocytoma 71 0.175
18
ADR040 Adrenal Gland Pheochromocytoma 46 0.175
19
HLX001 Helix Syndrome 47 0.175
20
P MYC084 Mycobacterium Tuberculosis 1 68 0.169
21
P PLM037 Pulmonary Hypertension 67 0.168
22
P HRP006 Herpes Simplex 65 0.168
23
P HRT032 Heart Disease 75 0.166
24
HYP066 Hyperglycemia 61 0.166
25
P SZR006 Seizure Disorder 56 0.165
26
VSL002 Visual Epilepsy 59 0.165
27
P RHN004 Rhinitis 57 0.162
28
P LKM071 Leukemia, Chronic Lymphocytic 79 0.162
29
BNR002 Bone Resorption Disease 48 0.161
30
INS024 Insulin-Like Growth Factor I 79 0.159
31
AST005 Asthma 76 0.158
32
ALL003 Allergic Rhinitis 67 0.156
33
P AST007 Astrocytoma 51 0.155
34
OST159 Osteogenic Sarcoma 66 0.155
35
HYP056 Hypoglycemia 66 0.154
36
c PRM005 Primary Hyperparathyroidism 58 0.152
37
ALL006 Allergic Asthma 56 0.152
38
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.152
39
P CRD119 Cardiac Arrest 67 0.151
40
PLR008 Pleurisy 50 0.150
41
ADN018 Adenoma 59 0.150
42
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.149
43
CHR074 Choriocarcinoma 47 0.148
44
P HYP076 Hyperthyroidism 55 0.148
45
P KDN018 Kidney Disease 72 0.148
46
P ATR011 Atrial Fibrillation 66 0.146
47
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.145
48
CYS001 Cystic Fibrosis 81 0.144
49
c ACT075 Acute Myocardial Infarction 57 0.144
50
P MNN013 Meningitis 66 0.144
51
LNG099 Lung Disease 60 0.143
52
P CLR023 Colorectal Cancer 99 0.143
53
P LVR013 Liver Disease 68 0.143
54
IMP005 Impotence 52 0.141
55
P TRM003 Tremor 54 0.141
56
P HYP086 Hypothyroidism 69 0.140
57
c PRC016 Pre-Eclampsia 63 0.138
58
c HYP595 Hypertension, Essential 84 0.138
59
P CRN300 Coronary Heart Disease 1 63 0.138
60
FTT001 Fatty Liver Disease 61 0.137
61
CRB004 Cerebral Artery Occlusion 45 0.136
62
ALL026 Allergic Hypersensitivity Disease 62 0.135
63
P GRV001 Graves' Disease 55 0.135
64
c MCR113 Microvascular Complications of Diabetes 3 52 0.134
65
c MCR120 Microvascular Complications of Diabetes 7 47 0.134
66
c MCR130 Microvascular Complications of Diabetes 6 41 0.134
67
c MCR133 Microvascular Complications of Diabetes 4 41 0.134
68
LVR012 Liver Cirrhosis 62 0.132
69
PTT037 Pituitary Tumors 44 0.131
70
P BRS047 Breast Cancer 97 0.130
71
GLB015 Glioblastoma Multiforme 75 0.129
72
CYT002 Cytokine Deficiency 42 0.128
73
P LYM118 Lymphoma 68 0.128
74
P HML002 Hemolytic Anemia 63 0.128
75
c SYS001 Systemic Lupus Erythematosus 86 0.127
76
P PRK057 Parkinson Disease, Late-Onset 78 0.126
77
P VSC007 Vascular Disease 63 0.126
78
ANG054 Angina Pectoris 66 0.125
79
SPN186 Spinal Cord Injury 60 0.125
80
WLF001 Wolff-Parkinson-White Syndrome 66 0.124
81
P HNT016 Huntington Disease 72 0.123
82
HMN044 Human Immunodeficiency Virus Type 1 71 0.121
83
P ADN016 Adenocarcinoma 64 0.119
84
P NRP001 Neuropathy 56 0.119
85
P OVR042 Ovarian Cancer 88 0.119
86
LYM027 Lymphopenia 58 0.119
87
THY029 Thyroid Carcinoma 59 0.119
88
IGR001 Ige Responsiveness, Atopic 59 0.119
89
P MYC007 Myocardial Infarction 70 0.118
90
P LKM062 Leukemia, Acute Lymphoblastic 69 0.117
91
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.117
92
HYP060 Hyperinsulinism 54 0.117
93
PRT036 Peritonitis 64 0.117
94
P DBT005 Diabetes Insipidus 55 0.117
95
c ACT073 Acute Leukemia 58 0.116
96
P MYL006 Myeloid Leukemia 60 0.116
97
SYN036 Syncope 45 0.116
98
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.115
99
P DRM053 Dermatitis, Atopic 66 0.115
100
OCL069 Ocular Motor Apraxia 51 0.114
101
BRN071 Brain Injury 49 0.113
102
P PSD015 Pseudohypoparathyroidism 56 0.113
103
DPR016 Depression 63 0.113
104
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.113
105
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.112
106
MYL069 Myeloma, Multiple 85 0.112
107
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.111
108
ATM095 Autoimmune Disease 62 0.111
109
P HYP024 Hypoparathyroidism 56 0.110
110
VCC001 Vaccinia 49 0.110
111
c HYP836 Hypercholesterolemia, Familial, 1 73 0.110
112
TXC005 Toxic Shock Syndrome 62 0.110
113
PNG002 Pain Agnosia 51 0.108
114
c HPT016 Hepatitis B 59 0.108
115
P PSR002 Psoriasis 62 0.108
116
PST011 Pustulosis of Palm and Sole 52 0.108
117
MST004 Mast Cell Neoplasm 42 0.107
118
EXT007 Extracutaneous Mastocytoma 38 0.107
119
P RHM011 Rheumatoid Arthritis 80 0.107
120
DBT010 Diabetic Neuropathy 54 0.106
121
PLM001 Pulmonary Tuberculosis 69 0.104
122
P LTR001 Lateral Sclerosis 54 0.104
123
DRM006 Dermatitis 61 0.103
124
P ALZ034 Alzheimer Disease 88 0.103
125
P SCK005 Sickle Cell Disease 50 0.103
126
c ACT071 Acute Kidney Failure 60 0.103
127
P GRF003 Graft-Versus-Host Disease 72 0.102
128
DFC004 Deficiency Anemia 70 0.101
129
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.101
130
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.099
131
ANX010 Anxiety 73 0.098
132
TTN003 Tetanus 65 0.098
133
GST033 Gestational Diabetes 61 0.098
134
PPT005 Peptic Ulcer Disease 59 0.098
135
PLM010 Pulmonary Edema 54 0.098
136
P ENC004 Encephalitis 61 0.096
137
P HYP098 Hypereosinophilic Syndrome 67 0.096
138
P MCR115 Microvascular Complications of Diabetes 5 66 0.096
139
P DBT009 Diabetes Mellitus 64 0.096
140
c HPT073 Hepatitis C Virus 72 0.095
141
TRM010 Traumatic Brain Injury 51 0.095
142
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.094
143
P BCL017 B-Cell Lymphoma 58 0.093
144
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.093
145
P PLM036 Pulmonary Fibrosis 65 0.093
146
ATH013 Atherosclerosis Susceptibility 65 0.093
147
P PRS040 Prostate Cancer 97 0.093
148
P VSC011 Vasculitis 62 0.092
149
PPL052 Papillomatosis, Confluent and Reticulated 33 0.092
150
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.091
151
MTB004 Metabolic Acidosis 50 0.090
152
c CHR684 Chronic Kidney Disease 70 0.090
153
P PNC035 Pancreatic Cancer 84 0.090
154
c SVR001 Severe Acute Respiratory Syndrome 62 0.089
155
P GST053 Gastric Cancer 83 0.089
156
c DLT002 Dilated Cardiomyopathy 79 0.089
157
P LPS004 Lupus Erythematosus 61 0.089
158
ADR016 Adrenal Cortical Carcinoma 48 0.088
159
ADR004 Adrenal Cortical Adenocarcinoma 39 0.088
160
P GLM007 Glomerulonephritis 57 0.087
161
c LKM061 Leukemia, Acute Myeloid 84 0.087
162
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.087
163
CHC001 Chickenpox 60 0.087
164
LPD008 Lipid Metabolism Disorder 62 0.086
165
ERY051 Erythroleukemia, Familial 56 0.086
166
P LNG032 Lung Cancer 98 0.085
167
P MLN008 Melanoma 69 0.085
168
c BCT007 Bacterial Meningitis 55 0.085
169
P INF037 Inflammatory Bowel Disease 54 0.085
170
P NTR004 Neutropenia 63 0.085
171
P BLD134 Bladder Cancer 79 0.084
172
MNT002 Mental Depression 58 0.084
173
RCK004 Rickets 68 0.084
174
INS001 Insulinoma 60 0.084
175
P THR014 Thrombocytopenia 67 0.084
176
GTR002 Goiter 53 0.084
177
c VRL010 Viral Hepatitis 52 0.084
178
LYM019 Lymphosarcoma 46 0.084
179
CLT003 Colitis 62 0.083
180
STR067 Stroke, Ischemic 81 0.083
181
RTN023 Retinitis 46 0.082
182
NRR001 Neuroretinitis 42 0.082
183
STT001 Status Epilepticus 60 0.082
184
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.082
185
P PRP019 Peripheral Nervous System Disease 58 0.082
186
P MJR001 Major Depressive Disorder 68 0.081
187
WTH001 Withdrawal Disorder 48 0.081
188
TRN015 Transient Cerebral Ischemia 63 0.081
189
END086 End Stage Renal Disease 51 0.081
190
RNL077 Renal Fibrosis 47 0.081
191
c ATR087 Atrial Standstill 1 75 0.081
192
SLP001 Sleeping Sickness 54 0.081
193
P BPL003 Bipolar Disorder 56 0.080
194
c MJR024 Major Affective Disorder 9 41 0.080
195
c MJR022 Major Affective Disorder 8 38 0.080
196
c GRV008 Graves Disease 1 56 0.080
197
P DRR001 Diarrhea 55 0.080
198
MSL001 Measles 62 0.079
199
DPH001 Diphtheria 60 0.079
200
MLR004 Malaria 81 0.078
201
INT007 Intermediate Coronary Syndrome 55 0.077
202
ACQ007 Acquired Immunodeficiency Syndrome 60 0.077
203
STM007 Stomatitis 50 0.077
204
47X002 47,xyy 49 0.077
205
P MSC005 Muscular Dystrophy 66 0.076
206
P CHR012 Chronic Granulomatous Disease 67 0.076
207
P PLY014 Polycystic Kidney Disease 62 0.076
208
c LKM063 Leukemia, Chronic Myeloid 72 0.076
209
CLN015 Colon Adenocarcinoma 65 0.076
210
SKN016 Skin Disease 63 0.076
211
TRT001 Teratocarcinoma 45 0.075
212
LYD001 Leydig Cell Tumor 45 0.075
213
P HPT023 Hepatocellular Carcinoma 100 0.075
214
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.075
215
P MLT020 Multiple Sclerosis 72 0.075
216
P ART022 Arthritis 69 0.075
217
BCT022 Bacterial Infectious Disease 56 0.074
218
P ECL001 Eclampsia 50 0.074
219
BRN004 Brain Edema 56 0.074
220
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.074
221
IRN002 Iron Metabolism Disease 57 0.074
222
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 25 0.073
223
ALC007 Alcohol Dependence 66 0.073
224
P RTN008 Retinitis Pigmentosa 79 0.073
225
P DYS154 Dystonia 65 0.073
226
MDD011 Mood Disorder 62 0.073
227
THR024 Thrombosis 57 0.073
228
URT010 Ureteral Obstruction 45 0.073
229
c PCH010 Pachyonychia Congenita 3 44 0.073
230
ALL014 Allergic Encephalomyelitis 38 0.072
231
P CNR004 Cone-Rod Dystrophy 2 73 0.072
232
PRS045 Prostatic Hypertrophy 53 0.072
233
PRT029 Parathyroid Adenoma 50 0.071
234
ESP021 Esophageal Cancer 90 0.071
235
CRB039 Cerebrovascular Disease 67 0.071
236
P MYP006 Myopia 55 0.071
237
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.071
238
HMP009 Haemophilus Influenzae 43 0.071
239
OVR094 Ovarian Epithelial Cancer 38 0.071
240
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.071
241
P SLP006 Sleep Apnea 69 0.070
242
P ALC033 Alcohol Use Disorder 58 0.070
243
HYP005 Hypokalemia 55 0.070
244
LWC001 Low Compliance Bladder 43 0.070
245
P RTN024 Retinoblastoma 73 0.069
246
DWN001 Down Syndrome 70 0.069
247
PST028 Post-Traumatic Stress Disorder 58 0.069
248
c FML008 Familial Retinoblastoma 53 0.069
249
ACT084 Acute Stress Disorder 47 0.069
250
P SRC025 Sarcoidosis 1 70 0.069
251
P RSP003 Respiratory Failure 74 0.069
252
GT001 Gout 64 0.069
253
P INF032 Infertility 57 0.069
254
PLY150 Polykaryocytosis Inducer 31 0.069
255
P PNM007 Pneumonia 68 0.069
256
AMN003 Amnestic Disorder 54 0.069
257
c ACT027 Acute Pancreatitis 60 0.068
258
c LKM005 Leukemia, T-Cell, Chronic 34 0.068
259
BRN024 Bronchitis 68 0.067
260
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.067
261
LSC001 Lesch-Nyhan Syndrome 62 0.067
262
CHL068 Cholestasis 61 0.067
263
P FBR017 Fibrosarcoma 56 0.067
264
P THY032 Thyroiditis 52 0.067
265
ARG004 Argyria 27 0.067
266
MYL009 Myelodysplastic Syndrome 70 0.066
267
P GST044 Gastritis 56 0.066
268
c SCN007 Secondary Hyperparathyroidism 51 0.066
269
P MYS003 Myasthenia Gravis 68 0.065
270
GST023 Gastric Ulcer 53 0.065
271
TRY001 Trypanosomiasis 50 0.065
272
HYP017 Hypophosphatemia 50 0.065
273
P PLY011 Polycystic Ovary Syndrome 56 0.064
274
P MLN007 Male Infertility 55 0.064
275
PRS021 Prostatic Adenoma 51 0.064
276
CRT015 Carotid Artery Occlusion 45 0.064
277
P ADL010 Adult Respiratory Distress Syndrome 65 0.064
278
THY122 Thyroid Gland Cancer 57 0.064
279
P MYP004 Myopathy 70 0.063
280
P BND020 Bone Disease 59 0.063
281
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.063
282
HPT004 Hepatic Coma 45 0.063
283
P SCH015 Schizophrenia 74 0.063
284
P ENC018 Encephalopathy 61 0.063
285
P UVT001 Uveitis 57 0.063
286
HRP004 Herpes Zoster 60 0.063
287
SCK003 Sickle Cell Anemia 74 0.062
288
PNC129 Pancreatic Adenocarcinoma 68 0.062
289
P END044 Endometriosis 63 0.062
290
PRS129 Prostatic Hyperplasia, Benign 49 0.062
291
URM002 Uremia 49 0.062
292
c ATM011 Autoimmune Hepatitis 63 0.061
293
MYX004 Myxedema 43 0.061
294
OST012 Osteoarthritis 78 0.061
295
CRV035 Cervical Cancer 76 0.061
296
P SYS005 Systemic Scleroderma 68 0.061
297
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.061
298
AGN016 Aging 56 0.061
299
ASP003 Aseptic Meningitis 51 0.061
300
RTN020 Retinal Vascular Disease 46 0.061
301
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.061
302
BRN002 Bronchiolitis 59 0.061
303
HRY003 Hairy Cell Leukemia 55 0.061
304
ATS010 Autosomal Recessive Disease 48 0.061
305
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.059
306
NRM005 Neuromuscular Disease 64 0.059
307
c WLM018 Wilms Tumor 5 61 0.059
308
PRT013 Portal Hypertension 59 0.059
309
BRN056 Bronchopulmonary Dysplasia 57 0.059
310
c MLG068 Malignant Glioma 46 0.059
311
P LNG064 Lung Cancer Susceptibility 3 78 0.059
312
ULC004 Ulcerative Colitis 73 0.059
313
P HYP061 Hypertrophic Cardiomyopathy 70 0.059
314
HYP014 Hyperuricemia 52 0.059
315
NTR046 Neutrophil Migration 50 0.059
317
P PRD008 Periodontitis 64 0.059
318
P MYC008 Myocarditis 59 0.059
319
P BRS044 Breast Adenocarcinoma 59 0.059
320
EYD002 Eye Disease 58 0.059
321
BRN012 Bronchiolitis Obliterans 55 0.059
322
P ART021 Arteriosclerosis 54 0.059
323
P RNV001 Renovascular Hypertension 48 0.059
324
MRP001 Morphine Dependence 41 0.059
325
KRT019 Keratitis, Hereditary 65 0.057
326
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.057
327
c SCL052 Scleroderma, Familial Progressive 61 0.057
328
P DNG005 Dengue Virus 59 0.057
329
P OST001 Osteopetrosis 70 0.057
330
LYM133 Lymphoma, Hodgkin, Classic 69 0.057
331
P HPT021 Hepatitis 67 0.057
332
c HPT001 Hepatitis C 62 0.057
333
P NPH012 Nephrotic Syndrome 60 0.057
334
P CTR002 Cataract 60 0.057
335
NPH009 Nephrolithiasis 55 0.057
336
LYM040 Lymphoblastic Lymphoma 54 0.057
337
c ACT135 Acute Graft Versus Host Disease 52 0.057
338
P OST002 Osteoporosis 74 0.056
339
P TRC086 Trichohepatoenteric Syndrome 1 62 0.056
340
INT002 Intermittent Claudication 61 0.056
341
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.056
342
GLC003 Glucose Intolerance 54 0.056
343
THR013 Thoracic Outlet Syndrome 54 0.056
344
c INH020 Inherited Metabolic Disorder 47 0.056
345
P DMN001 Diamond-Blackfan Anemia 69 0.055
346
P EXN002 Exanthem 57 0.055
347
HMC014 Homocysteinemia 53 0.055
348
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.054
349
SPL018 Splenomegaly 48 0.054
350
P VTR007 Vitreoretinopathy 46 0.054
351
c CHR064 Chronic Monocytic Leukemia 33 0.054
352
END057 Endometrial Cancer 74 0.054
353
CHG001 Chagas Disease 66 0.054
354
PLG002 Plague 63 0.054
355
P THL005 Thalassemia 60 0.054
356
ILT001 Ileitis 50 0.054
357
NWC001 Newcastle Disease 45 0.054
358
HND015 Hand Skill, Relative 33 0.054
359
ACR007 Acromegaly 71 0.053
360
ACT119 Acute Promyelocytic Leukemia 63 0.053
361
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.053
362
PLY023 Polycystic Liver Disease 57 0.053
363
P PTT006 Pituitary Adenoma 55 0.053
364
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.053
365
PPL002 Papillary Carcinoma 47 0.053
366
SPR126 Superior Semicircular Canal Dehiscence 40 0.053
367
c HMG029 Hemoglobin Se Disease 39 0.053
368
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.053
369
PLS037 Plasma Cell Tumor 22 0.053
370
P THY023 Thymoma 65 0.053
371
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.053
372
INT066 Interstitial Lung Disease 60 0.053
373
P OPT006 Optic Nerve Disease 60 0.053
374
NNL006 Non-Alcoholic Steatohepatitis 54 0.053
375
PRP016 Paraplegia 52 0.053
376
c THY107 Thymoma, Familial 52 0.053
377
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.053
378
ATX019 Ataxia with Vitamin E Deficiency 42 0.053
379
c MCR129 Microvascular Complications of Diabetes 1 66 0.051
380
P PRP029 Porphyria 62 0.051
381
c ACT134 Acute Liver Failure 56 0.051
382
LMB062 Limb Ischemia 55 0.051
383
DFF005 Diffuse Large B-Cell Lymphoma 55 0.051
384
P MNC007 Monocytic Leukemia 53 0.051
385
CLR109 Colorectal Adenocarcinoma 51 0.051
386
CRB090 Cerebral Hypoxia 44 0.051
387
P HYP265 Hypotonia 43 0.051
388
c MCR112 Microvascular Complications of Diabetes 2 41 0.051
389
ADG002 Audiogenic Seizures 25 0.051
390
c TBR025 Tuberous Sclerosis 1 77 0.051
391
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.051
392
GST040 Gastric Adenocarcinoma 70 0.051
393
P TBR001 Tuberous Sclerosis 70 0.051
394
IRR002 Irritable Bowel Syndrome 65 0.051
395
P INT068 Intestinal Disease 53 0.051
396
THY030 Thyroid Gland Disease 52 0.051
397
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.051
398
GST045 Gastroenteritis 59 0.049
399
PLS009 Plasma Cell Neoplasm 51 0.049
400
DWR001 Dwarfism 44 0.049
401
SCH014 Schistosomiasis 57 0.049
402
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.049
403
IMM136 Immune System Disease 45 0.049
404
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.049
405
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.049
406
WST005 West Nile Virus 54 0.049
407
PRN011 Pernicious Anemia 53 0.049
408
NRT004 Neuritis 52 0.049
409
c PRG020 Paragangliomas 3 39 0.049
410
THY111 Thyroid Carcinoma, Familial Medullary 67 0.047
411
CLF027 Cleft Palate, Isolated 64 0.047
412
P CRN038 Carney Complex Variant 61 0.047
413
P PLY019 Polyneuropathy 56 0.047
414
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.047
415
P CYS039 Cystic Kidney Disease 54 0.047
416
P RTN016 Retinal Degeneration 53 0.047
417
c VRL007 Viral Encephalitis 51 0.047
418
THY125 Thyroid Gland Medullary Carcinoma 50 0.047
419
P OPN001 Open-Angle Glaucoma 49 0.047
420
P HYP263 Hypersomnia 41 0.047
421
MYT011 Myotonia 34 0.047
422
SRC014 Sarcoma 65 0.046
423
P RHB003 Rhabdomyosarcoma 63 0.046
424
P HYP750 Hypertriglyceridemia, Familial 62 0.046
425
HPT019 Hepatic Encephalopathy 60 0.046
426
CNS004 Constipation 58 0.046
427
DSS009 Disseminated Intravascular Coagulation 57 0.046
428
P CHN012 Chondrosarcoma 56 0.046
429
PNC001 Pancytopenia 54 0.046
430
c DMN023 Diamond-Blackfan Anemia 1 53 0.046
431
NNT012 Neonatal Jaundice 53 0.046
432
P RTN018 Retinal Disease 53 0.046
433
P OVR082 Overgrowth Syndrome 50 0.046
434
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.046
435
c RTN047 Retinitis Pigmentosa 18 42 0.046
436
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.046
437
c CHR417 Chronic Graft Versus Host Disease 57 0.044
438
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.044
439
SXL003 Sexual Disorder 47 0.044
440
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.044
441
MYL005 Myelofibrosis 70 0.043
442
P TRN020 Turner Syndrome 67 0.043
443
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.043
444
P PRM006 Primary Biliary Cirrhosis 62 0.043
445
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.043
446
P GLL022 Guillain-Barre Syndrome 59 0.043
447
HPT022 Hepatoblastoma 56 0.043
448
MYM001 Myoma 54 0.043
449
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.043
450
OST011 Osteomalacia 52 0.043
451
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.043
452
NDL007 Nodular Goiter 47 0.043
453
PLL012 Pollen Allergy 46 0.043
454
P BRB001 Beriberi 46 0.043
455
c CRN278 Craniosynostosis 1 45 0.043
456
URL001 Urolithiasis 45 0.043
457
ADR041 Adrenal Cortical Adenoma 43 0.043
458
IDP073 Idiopathic Hypercalciuria 43 0.043
459
c HMP023 Hemophagocytic Lymphohistiocytosis, Familial, 5 41 0.043
460
LNG030 Lung Adenoma 39 0.043
461
c RTH007 Rothmund-Thomson Syndrome, Type 1 37 0.043
462
SCR003 Secretory Diarrhea 37 0.043
463
PFF001 Pfeiffer Syndrome 79 0.043
464
MYC006 Mycosis Fungoides 66 0.043
465
HYP020 Hyperprolactinemia 64 0.043
466
HSH003 Hashimoto Thyroiditis 62 0.043
467
RTN017 Retinal Detachment 61 0.043
468
CHL123 Chlamydia 59 0.043
469
PRT058 Pure Autonomic Failure 59 0.043
470
ANT024 Anthrax Disease 58 0.043
471
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.043
472
PLS011 Plasmacytoma 56 0.043
473
MCL006 Macular Retinal Edema 55 0.043
474
END040 Endogenous Depression 55 0.043
475
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.043
476
SPN035 Spindle Cell Sarcoma 53 0.043
477
c CHR418 Chronic Leukemia 49 0.043
478
MCR004 Macroglobulinemia 49 0.043
479
KRT002 Keratomalacia 47 0.043
480
ORL015 Oral Squamous Cell Carcinoma 43 0.043
481
HRW001 Hair Whorl 36 0.043
482
DSR074 Disorder of Purine Metabolism 29 0.043
483
PST092 Posttransplant Acute Limbic Encephalitis 29 0.043
484
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.040
485
c NRF023 Neurofibromatosis, Type Ii 80 0.040
486
c THR092 Thrombophilia Due to Thrombin Defect 73 0.040
487
APN008 Apnea, Obstructive Sleep 64 0.040
488
NRF007 Neurofibroma 64 0.040
489
P ANR048 Aniridia 1 63 0.040
490
END041 Endometrial Adenocarcinoma 63 0.040
491
ANR007 Anorexia Nervosa 63 0.040
492
c ANM038 Anemia, Autoimmune Hemolytic 62 0.040
493
ACN002 Acanthosis Nigricans 60 0.040
494
P URT039 Urticaria 58 0.040
495
P SLM003 Salmonellosis 55 0.040
496
DMY004 Demyelinating Disease 52 0.040
497
P ACT105 Acute Mountain Sickness 52 0.040
498
P LCT001 Lactic Acidosis 51 0.040
499
P CHL066 Cholangitis 51 0.040
500
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.040
501
P OBS001 Obstructive Jaundice 50 0.040
502
c CNG027 Congenital Hemolytic Anemia 50 0.040
503
SBS004 Substance Dependence 48 0.040
504
OPD006 Opioid Addiction 48 0.040
505
P PRD021 Periodic Paralysis 45 0.040
506
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.040
507
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.040
508
OCL052 Ocular Dominance 42 0.040
509
MCL003 Macular Holes 40 0.040
510
WLL004 Wallerian Degeneration 39 0.040
511
ATX010 Ataxia Neuropathy Spectrum 34 0.040
512
c PRG106 Progressive Muscular Dystrophy 33 0.040
513
ACT064 Acute Necrotizing Encephalitis 33 0.040
514
PLT016 Platelet Adenylate Cyclase Activity 16 0.040
515
BLD137 Blood Group--Ahonen 16 0.040
516
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.038
517
P FLL037 Follicular Lymphoma 67 0.038
518
CHD001 Chediak-Higashi Syndrome 66 0.038
519
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.038
520
NRL005 Neurilemmoma 60 0.038
521
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.038
522
PSD014 Pseudopseudohypoparathyroidism 55 0.038
523
MMM001 Mammary Paget's Disease 53 0.038
524
MGL001 Megaloblastic Anemia 51 0.038
525
ATY042 Atypical Chronic Myeloid Leukemia 49 0.038
526
CHL004 Cholelithiasis 49 0.038
527
CWP001 Cowpox 46 0.038
528
RSP021 Respiratory Allergy 45 0.038
529
SBC016 Subacute Delirium 44 0.038
530
ADN022 Adenylosuccinase Deficiency 44 0.038
531
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.038
532
CNN003 Conn's Syndrome 79 0.036
533
ADR007 Adrenoleukodystrophy 75 0.036
534
LGH007 Leigh Syndrome 70 0.036
535
P FRG001 Fragile X Syndrome 70 0.036
536
c RHB024 Rhabdomyosarcoma 2 67 0.036
537
c WLM013 Wilms Tumor 1 65 0.036
538
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.036
539
MSC007 Muscle Hypertrophy 64 0.036
540
c GLC092 Glaucoma, Primary Open Angle 62 0.036
541
c ALP101 Alpha-Thalassemia 62 0.036
542
VRC005 Varicose Veins 60 0.036
543
DSS008 Disease of Mental Health 58 0.036
544
P BNC003 Bone Cancer 58 0.036
545
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 0.036
546
P FTL001 Fetal Alcohol Syndrome 57 0.036
547
c LKM070 Leukemia, Acute Monocytic 57 0.036
548
CYT008 Cytomegalovirus Infection 57 0.036
549
MTH009 Mouth Disease 56 0.036
550
HMG005 Hemoglobinopathy 56 0.036
551
P NRF002 Neurofibromatosis 56 0.036
552
SML019 Smallpox 56 0.036
553
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.036
554
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.036
555
GNG005 Gangliocytoma 55 0.036
556
P PMP001 Pemphigus 54 0.036
557
P HYP083 Hypopituitarism 53 0.036
558
P PTS002 Ptosis 53 0.036
559
c OST131 Osteopetrosis, Autosomal Dominant 2 53 0.036
560
GNG002 Ganglioneuroma 52 0.036
561
P RCT021 Rectum Cancer 52 0.036
562
ACT200 Acute Monoblastic Leukemia 52 0.036
563
THR004 Thrombocytosis 51 0.036
564
P SPP010 Suppressor of Tumorigenicity 3 51 0.036
565
c SVR005 Severe Pre-Eclampsia 50 0.036
566
ECT026 Ectopic Pregnancy 50 0.036
567
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.036
568
MDD018 Middle East Respiratory Syndrome 43 0.036
569
SNL007 Senile Cataract 42 0.036
570
PST053 Postherpetic Neuralgia 40 0.036
571
PLY100 Polyploidy 40 0.036
572
P PRC031 Preeclampsia/eclampsia 1 38 0.036
573
ADR022 Adrenomyeloneuropathy 38 0.036
574
CGH001 Cough Variant Asthma 37 0.036
576
AST002 Astroblastoma 34 0.036
577
c BLD140 Blood Group, I System 32 0.036
578
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.036
579
PNF002 Painful Legs and Moving Toes Syndrome 14 0.036
580
BRN028 Brain Cancer 74 0.031
581
P FML011 Familial Adenomatous Polyposis 72 0.031
582
MCC012 Mccune-Albright Syndrome 70 0.031
583
P TTR001 Tetralogy of Fallot 70 0.031
584
PLY001 Polycythemia Vera 69 0.031
585
P INF038 Influenza 68 0.031
586
P PRP003 Porphyria Cutanea Tarda 67 0.031
587
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.031
588
P SKN015 Skin Carcinoma 66 0.031
589
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.031
590
LBR036 Leber Plus Disease 66 0.031
591
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.031
592
CLR108 Colorectal Adenoma 64 0.031
593
DSM004 Desmoid Tumor 64 0.031
594
HMT002 Hematologic Cancer 62 0.031
595
OST003 Osteonecrosis 61 0.031
596
SDD001 Sudden Infant Death Syndrome 61 0.031
597
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.031
598
DNG002 Dengue Hemorrhagic Fever 60 0.031
599
P MCR010 Microcephaly 59 0.031
600
FML063 Familial Glucocorticoid Deficiency 58 0.031
601
ADR005 Adrenal Carcinoma 58 0.031
602
CHL028 Childhood Type Dermatomyositis 58 0.031
603
c DWL002 Dowling-Degos Disease 1 58 0.031
604
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.031
605
PMP006 Pemphigus Vulgaris, Familial 57 0.031
606
P GLL020 Gallbladder Disease 57 0.031
607
MCR013 Microphthalmia 57 0.031
608
P PLY018 Polycythemia 56 0.031
609
HPT046 Hepatic Veno-Occlusive Disease 56 0.031
610
P MLT074 Multiple Endocrine Neoplasia 56 0.031
611
ISL001 Islet Cell Tumor 56 0.031
612
SNS003 Sensory Peripheral Neuropathy 54 0.031
613
P LCH002 Lichen Planus 53 0.031
614
P END047 Endophthalmitis 53 0.031
615
P INS002 in Situ Carcinoma 53 0.031
616
P RNL017 Renal Oncocytoma 53 0.031
617
CLF001 Cleft Lip 53 0.031
618
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 53 0.031
619
OVR059 Ovary Adenocarcinoma 53 0.031
620
CHN054 Chondrodysplasia, Blomstrand Type 52 0.031
621
DRM011 Dermatophytosis 52 0.031
622
HRP009 Herpes Simplex Encephalitis 52 0.031
623
P BRT004 Bartter Disease 52 0.031
624
c HYP243 Hyperparathyroidism 1 51 0.031
625
c NMN014 Niemann-Pick Disease, Type C2 51 0.031
626
MTP034 Metaphyseal Chondrodysplasia, Jansen Type 51 0.031
627
ESP002 Esophageal Varix 51 0.031
628
HND002 Hand, Foot and Mouth Disease 51 0.031
629
SGW002 Segawa Syndrome, Autosomal Recessive 51 0.031
630
ACT017 Acute Chest Syndrome 51 0.031
631
LNT004 Lentigines 50 0.031
632
c PYR010 Peyronie's Disease 50 0.031
633
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.031
634
P PNV001 Panuveitis 50 0.031
635
RNL011 Renal Osteodystrophy 50 0.031
636
ERY004 Erysipelas 49 0.031
637
P CTN015 Cutaneous T Cell Lymphoma 49 0.031
638
c 46X049 46,xy Sex Reversal 2 48 0.031
639
DBT006 Diabetic Macular Edema 48 0.031
640
FBR009 Fibrous Dysplasia 48 0.031
641
RCT020 Rectum Adenocarcinoma 48 0.031
642
VTM002 Vitamin B12 Deficiency 48 0.031
643
PRL017 Prolymphocytic Leukemia 47 0.031
644
THY128 Thyroid Tumor 47 0.031
645
ANV001 Anovulation 47 0.031
646
RYN005 Raynaud Phenomenon 47 0.031
647
P MTH007 Methemoglobinemia 46 0.031
648
GRW007 Growth Hormone Deficiency 46 0.031
649
LKS001 Leukostasis 46 0.031
650
c SBC007 Subacute Thyroiditis 45 0.031
651
RTR001 Retrograde Amnesia 44 0.031
652
P END039 Endodermal Sinus Tumor 44 0.031
653
IDP033 Idiopathic Edema 44 0.031
654
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.031
655
ANC002 Anca-Associated Vasculitis 41 0.031
656
DDN003 Duodenum Adenocarcinoma 41 0.031
657
PRS063 Paresthesia 41 0.031
658
ISL151 Isolated Elevated Serum Creatine Phosphokinase Levels 40 0.031
659
TST018 Testicular Yolk Sac Tumor 39 0.031
660
MYP001 Myoepithelioma 38 0.031
661
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.031
662
HRM003 Hormone Producing Pituitary Cancer 37 0.031
663
P FML187 Familial Hypertension 37 0.031
664
HYP026 Hypoglycemic Coma 36 0.031
665
c CRN277 Craniosynostosis 2 36 0.031
666
WHP002 Whiplash 36 0.031
667
INT040 Intrinsic Asthma 34 0.031
668
PTT001 Pituitary Hypoplasia 34 0.031
669
TQP001 Taqi Polymorphism 32 0.031
670
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.031
671
c PSD104 Pseudohypoparathyroidism, Type Ii 31 0.031
672
SNG003 Single Ventricular Heart 30 0.031
673
GRV012 Grover's Disease 30 0.031
674
MNN024 Meningitis and Encephalitis 29 0.031
675
BYS001 Byssinosis 28 0.031
676
MYB001 Myoblastoma 28 0.031
677
GLC043 Glucocorticoid Deficiency 2 27 0.031
678
PRQ002 Paraquat Poisoning 26 0.031
679
INV018 Invasive Mole 25 0.031
680
HDG004 Hodgkin's Granuloma 23 0.031
681
HVY002 Heavy Metal Poisoning 22 0.031
682
HDG006 Hodgkin's Paragranuloma 22 0.031
683
HML018 Homologous Wasting Disease 22 0.031
684
P HRD221 Hereditary Nephrogenic Diabetes Insipidus 17 0.031
685
NCL008 Nuclear Ribonucleic Acid 16 0.031
686
DSR013 Disorders of Gnas Inactivation 14 0.031
Content
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