Search results for cyclic amp

792 hits were found for cyclic amp

# Family MCID Name MIFTS Score
1
CHL014 Cholera 58 0.667
2
PRT037 Pertussis 66 0.521
3
P NRB010 Neuroblastoma 1 66 0.430
4
P GLM045 Glioma 64 0.352
5
GLL048 Glial Tumor 48 0.351
6
P PHC003 Pheochromocytoma 71 0.274
7
ADR040 Adrenal Gland Pheochromocytoma 51 0.274
8
P NTR004 Neutropenia 64 0.257
9
BNR002 Bone Resorption Disease 51 0.246
10
P HYP069 Hyperparathyroidism 64 0.240
11
48X005 48,xyyy 37 0.224
12
HLX001 Helix Syndrome 46 0.215
13
c PRM005 Primary Hyperparathyroidism 60 0.211
14
HYP266 Hypoxia 58 0.205
15
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.203
16
P AST007 Astrocytoma 52 0.198
17
ISC004 Ischemia 62 0.190
18
OST159 Osteogenic Sarcoma 67 0.189
19
HYP066 Hyperglycemia 63 0.186
20
P PSR002 Psoriasis 63 0.181
21
PST011 Pustulosis of Palm and Sole 51 0.181
22
CHR074 Choriocarcinoma 47 0.178
23
FTT001 Fatty Liver Disease 63 0.176
24
CYS001 Cystic Fibrosis 84 0.172
25
c MGR028 Migraine with or Without Aura 1 70 0.170
26
INS024 Insulin-Like Growth Factor I 79 0.168
27
ADN018 Adenoma 60 0.168
28
CYT002 Cytokine Deficiency 46 0.168
29
P LKM002 Leukemia 69 0.168
30
CNG034 Congestive Heart Failure 69 0.164
31
P VSC007 Vascular Disease 65 0.164
32
PTT037 Pituitary Tumors 47 0.163
33
HYP056 Hypoglycemia 68 0.163
34
ANX004 Anoxia 44 0.162
35
P CLR023 Colorectal Cancer 100 0.155
36
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.154
37
P LYM031 Lymphocytic Leukemia 56 0.151
38
P HYP086 Hypothyroidism 70 0.151
39
P BRS047 Breast Cancer 99 0.148
40
IMP005 Impotence 53 0.147
41
P HRT032 Heart Disease 78 0.146
42
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.146
43
P RHM011 Rheumatoid Arthritis 82 0.146
44
P HYP076 Hyperthyroidism 55 0.146
45
P LVR013 Liver Disease 71 0.144
46
GLB002 Glioblastoma 74 0.141
47
GLB015 Glioblastoma Multiforme 60 0.141
48
HRW001 Hair Whorl 36 0.139
49
P THR014 Thrombocytopenia 67 0.138
50
MLN008 Melanoma 68 0.138
51
P HRP006 Herpes Simplex 66 0.138
52
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.136
53
PPL052 Papillomatosis, Confluent and Reticulated 34 0.135
54
c HYP595 Hypertension, Essential 87 0.135
55
ATM095 Autoimmune Disease 62 0.134
56
P SZR006 Seizure Disorder 59 0.134
57
P PLM037 Pulmonary Hypertension 69 0.133
58
VSL002 Visual Epilepsy 58 0.133
59
P KDN018 Kidney Disease 73 0.132
60
P LYM118 Lymphoma 70 0.131
61
P OST002 Osteoporosis 79 0.130
62
TRT001 Teratocarcinoma 44 0.130
63
P TCL004 T-Cell Leukemia 48 0.130
64
c LKM005 Leukemia, T-Cell, Chronic 35 0.130
65
P DRM053 Dermatitis, Atopic 68 0.129
66
DPR016 Depression 64 0.128
67
BCT022 Bacterial Infectious Disease 57 0.128
68
P RTN024 Retinoblastoma 74 0.126
69
c FML008 Familial Retinoblastoma 46 0.126
70
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.125
71
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.125
72
ALL026 Allergic Hypersensitivity Disease 65 0.125
73
P PSD015 Pseudohypoparathyroidism 54 0.124
74
c ACT210 Acute Respiratory Distress Syndrome 59 0.124
75
ALL014 Allergic Encephalomyelitis 40 0.123
76
PNG002 Pain Agnosia 52 0.123
77
LVR012 Liver Cirrhosis 67 0.123
78
P ADN016 Adenocarcinoma 65 0.123
79
47X002 47,xyy 49 0.123
80
DRM006 Dermatitis 63 0.122
81
P END044 Endometriosis 63 0.122
82
AST005 Asthma 80 0.122
83
STM007 Stomatitis 51 0.121
84
P PRS040 Prostate Cancer 97 0.121
85
SPN186 Spinal Cord Injury 63 0.120
86
LPD008 Lipid Metabolism Disorder 64 0.119
87
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.119
88
c ACT073 Acute Leukemia 59 0.117
89
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.117
90
MST004 Mast Cell Neoplasm 40 0.116
91
EXT007 Extracutaneous Mastocytoma 39 0.116
92
EMB004 Embryonal Carcinoma 57 0.116
93
P HPT023 Hepatocellular Carcinoma 99 0.115
94
P MYL006 Myeloid Leukemia 61 0.115
95
P DRR001 Diarrhea 55 0.114
96
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.114
97
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.113
98
P FBR017 Fibrosarcoma 57 0.112
99
P GRV001 Graves' Disease 57 0.112
100
P PLY014 Polycystic Kidney Disease 61 0.111
101
TTN003 Tetanus 62 0.111
102
THY029 Thyroid Carcinoma 62 0.111
103
P MYP004 Myopathy 63 0.110
104
P DBT005 Diabetes Insipidus 54 0.110
105
P OVR042 Ovarian Cancer 89 0.109
106
INS001 Insulinoma 60 0.108
107
P LNG032 Lung Cancer 99 0.107
108
P HYP024 Hypoparathyroidism 56 0.107
109
c SYS001 Systemic Lupus Erythematosus 88 0.107
110
P ALZ034 Alzheimer Disease 90 0.106
111
P PNC035 Pancreatic Cancer 86 0.106
112
c ATR087 Atrial Standstill 1 76 0.106
113
P LKM062 Leukemia, Acute Lymphoblastic 68 0.106
114
P PLY011 Polycystic Ovary Syndrome 58 0.106
115
AGN016 Aging 58 0.106
116
CHL068 Cholestasis 61 0.104
117
HYP060 Hyperinsulinism 55 0.104
118
OCL069 Ocular Motor Apraxia 53 0.104
119
HMN044 Human Immunodeficiency Virus Type 1 73 0.103
120
c PRC016 Pre-Eclampsia 63 0.103
121
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.102
122
P ENC018 Encephalopathy 64 0.101
123
MNT002 Mental Depression 60 0.099
124
P RHN004 Rhinitis 59 0.098
125
ATH013 Atherosclerosis Susceptibility 68 0.097
126
P BPL003 Bipolar Disorder 59 0.096
127
c MJR024 Major Affective Disorder 9 42 0.096
128
c MJR022 Major Affective Disorder 8 39 0.096
129
PLY150 Polykaryocytosis Inducer 31 0.096
130
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.096
131
P TRM003 Tremor 55 0.095
132
GLC003 Glucose Intolerance 55 0.095
133
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.094
134
P PRD008 Periodontitis 66 0.094
135
c HYP836 Hypercholesterolemia, Familial, 1 74 0.093
136
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.093
137
c PCH010 Pachyonychia Congenita 3 43 0.093
138
ALL003 Allergic Rhinitis 69 0.092
139
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.092
140
P MSC005 Muscular Dystrophy 68 0.091
141
c SCN007 Secondary Hyperparathyroidism 52 0.091
142
c MLG068 Malignant Glioma 46 0.091
143
PST092 Posttransplant Acute Limbic Encephalitis 29 0.090
144
SRC014 Sarcoma 67 0.089
145
SPN035 Spindle Cell Sarcoma 57 0.089
146
c MCR113 Microvascular Complications of Diabetes 3 55 0.089
147
c MCR120 Microvascular Complications of Diabetes 7 48 0.089
148
c MCR130 Microvascular Complications of Diabetes 6 42 0.089
149
c MCR133 Microvascular Complications of Diabetes 4 42 0.089
150
c HPT073 Hepatitis C Virus 74 0.089
151
LNG099 Lung Disease 62 0.089
152
CHL123 Chlamydia 60 0.088
153
P HYP061 Hypertrophic Cardiomyopathy 68 0.088
154
MYL069 Myeloma, Multiple 85 0.088
155
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.088
156
ERY051 Erythroleukemia, Familial 58 0.088
157
P MJR007 Major Affective Disorder 1 44 0.088
158
P BCL017 B-Cell Lymphoma 61 0.086
159
GTR002 Goiter 54 0.086
160
c DLT002 Dilated Cardiomyopathy 81 0.086
161
BRN071 Brain Injury 51 0.086
162
TXC005 Toxic Shock Syndrome 63 0.085
163
P HDC001 Headache 59 0.085
164
P INF037 Inflammatory Bowel Disease 57 0.085
165
P MJR001 Major Depressive Disorder 69 0.085
166
c SML038 Small Cell Cancer of the Lung 67 0.085
167
c ACT071 Acute Kidney Failure 60 0.085
168
P ART022 Arthritis 71 0.084
169
P RTN016 Retinal Degeneration 56 0.084
170
P HYP750 Hypertriglyceridemia, Familial 62 0.084
171
P HYP098 Hypereosinophilic Syndrome 67 0.083
172
NTR046 Neutrophil Migration 49 0.083
173
CRB004 Cerebral Artery Occlusion 38 0.083
174
P SCH015 Schizophrenia 76 0.083
175
c LKM071 Leukemia, Chronic Lymphocytic 81 0.082
176
c LKM004 Leukemia, B-Cell, Chronic 35 0.082
177
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 20 0.082
178
c LKM061 Leukemia, Acute Myeloid 84 0.082
179
IMM167 Immune Deficiency Disease 79 0.082
180
P NRF023 Neurofibromatosis, Type Ii 77 0.081
181
LYM019 Lymphosarcoma 48 0.081
182
P LPS004 Lupus Erythematosus 62 0.081
183
P INF032 Infertility 60 0.081
184
STT001 Status Epilepticus 61 0.081
185
WTH001 Withdrawal Disorder 47 0.081
186
P CRN018 Coronary Artery Anomaly 67 0.080
187
END030 End Stage Renal Failure 60 0.080
188
ADR016 Adrenal Cortical Carcinoma 51 0.080
189
VCC001 Vaccinia 50 0.080
190
ADR004 Adrenal Cortical Adenocarcinoma 44 0.080
191
CNN003 Conn's Syndrome 78 0.080
192
P BLD134 Bladder Cancer 79 0.079
193
MSC007 Muscle Hypertrophy 65 0.079
194
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.079
195
c PSD108 Pseudohypoparathyroidism, Type Ia 61 0.079
196
SKN016 Skin Disease 64 0.079
197
PPT005 Peptic Ulcer Disease 60 0.079
198
ANX010 Anxiety 75 0.079
199
END057 Endometrial Cancer 74 0.079
200
P CND004 Candidiasis 61 0.078
201
BRN024 Bronchitis 70 0.077
202
ALL006 Allergic Asthma 56 0.077
203
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.077
204
WLF001 Wolff-Parkinson-White Syndrome 65 0.076
205
PLM010 Pulmonary Edema 56 0.076
206
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.076
207
CLN015 Colon Adenocarcinoma 65 0.076
208
BND020 Bone Disease 60 0.076
209
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.075
211
HPT004 Hepatic Coma 42 0.075
212
c ADL017 Adult T-Cell Leukemia 59 0.075
213
P PTT006 Pituitary Adenoma 53 0.075
214
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.074
215
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.074
216
c ACT075 Acute Myocardial Infarction 59 0.074
217
c SCL052 Scleroderma, Familial Progressive 62 0.074
218
CRV035 Cervical Cancer 77 0.074
219
P TBR001 Tuberous Sclerosis 72 0.074
220
P MYC007 Myocardial Infarction 74 0.074
221
MSL001 Measles 61 0.074
222
P ECL001 Eclampsia 53 0.074
223
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.073
224
P MYC008 Myocarditis 60 0.073
225
P MLT020 Multiple Sclerosis 73 0.073
226
HYP005 Hypokalemia 55 0.072
227
P DDN001 Duodenal Ulcer 50 0.072
228
P CRN038 Carney Complex Variant 63 0.072
229
ENH001 Enhanced S-Cone Syndrome 56 0.072
230
P CHR345 Chronic Pain 52 0.072
231
ANV001 Anovulation 47 0.071
232
P MSC003 Muscular Atrophy 52 0.071
233
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.071
234
MLR004 Malaria 82 0.071
235
P VSC011 Vasculitis 64 0.070
236
DMY004 Demyelinating Disease 54 0.070
237
c CHR684 Chronic Kidney Disease 68 0.070
238
P GST053 Gastric Cancer 85 0.070
239
P ATS364 Autism 68 0.070
240
c HPT016 Hepatitis B 63 0.070
241
ADL002 Adult Syndrome 62 0.070
242
SQM006 Squamous Cell Carcinoma 60 0.070
243
c GRV008 Graves Disease 1 55 0.069
244
P SLP006 Sleep Apnea 71 0.069
245
BRS051 Breast Disease 59 0.069
246
c TBR025 Tuberous Sclerosis 1 74 0.069
247
c LKM063 Leukemia, Chronic Myeloid 74 0.069
248
P SYS005 Systemic Scleroderma 68 0.069
249
P ATR011 Atrial Fibrillation 67 0.069
250
P RHB003 Rhabdomyosarcoma 62 0.068
251
P MDL005 Medulloblastoma 78 0.068
252
ALC007 Alcohol Dependence 68 0.068
253
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.067
254
SVR004 Severe Combined Immunodeficiency 74 0.067
255
P MCR115 Microvascular Complications of Diabetes 5 67 0.067
256
P CRD119 Cardiac Arrest 71 0.067
257
P EPL164 Epilepsy 73 0.067
258
LYM017 Lyme Disease 64 0.067
259
DYS015 Dysentery 45 0.067
260
MYL009 Myelodysplastic Syndrome 72 0.066
261
LSH001 Leishmaniasis 64 0.066
262
P KLZ004 Kala-Azar 1 43 0.066
263
IDP011 Idiopathic Interstitial Pneumonia 65 0.065
264
MDD011 Mood Disorder 62 0.065
265
CRB039 Cerebrovascular Disease 71 0.065
266
P MNN013 Meningitis 67 0.065
267
ANG054 Angina Pectoris 66 0.065
268
P ALC033 Alcohol Use Disorder 58 0.065
269
PLM017 Pulmonary Alveolar Microlithiasis 54 0.065
270
P ATX030 Ataxia-Telangiectasia 83 0.065
271
RNL077 Renal Fibrosis 49 0.065
272
URT010 Ureteral Obstruction 46 0.065
273
c PSD117 Pseudohypoparathyroidism, Type Ic 38 0.065
274
CRH001 Crohn's Disease 75 0.065
275
P LNG064 Lung Cancer Susceptibility 3 79 0.064
276
P PLM036 Pulmonary Fibrosis 66 0.064
277
P MYS003 Myasthenia Gravis 68 0.063
278
c ACT027 Acute Pancreatitis 60 0.063
279
P LTR001 Lateral Sclerosis 56 0.063
280
MTB004 Metabolic Acidosis 48 0.063
281
MRP001 Morphine Dependence 41 0.063
282
PLM001 Pulmonary Tuberculosis 72 0.063
283
CHG001 Chagas Disease 66 0.063
284
P NPH012 Nephrotic Syndrome 65 0.063
285
P END033 Endocarditis 58 0.063
286
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 53 0.063
287
PLR008 Pleurisy 50 0.063
288
SPL018 Splenomegaly 48 0.063
289
P MYC033 Myoclonus 47 0.063
290
HMP009 Haemophilus Influenzae 46 0.063
291
P LYD001 Leydig Cell Tumor 45 0.063
292
CRT015 Carotid Artery Occlusion 44 0.063
293
DFC004 Deficiency Anemia 77 0.063
294
DWN001 Down Syndrome 70 0.063
295
P NRP001 Neuropathy 57 0.063
296
GT001 Gout 63 0.062
297
ACQ007 Acquired Immunodeficiency Syndrome 61 0.062
298
P GLY013 Glycogen Storage Disease 59 0.062
299
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.062
300
P ENC004 Encephalitis 64 0.062
301
HPT019 Hepatic Encephalopathy 60 0.062
302
P DNG005 Dengue Virus 57 0.062
303
OST012 Osteoarthritis 80 0.061
304
P INT143 Interstitial Cystitis 62 0.061
305
P PNM007 Pneumonia 71 0.061
306
NRL005 Neurilemmoma 62 0.061
307
c HPT001 Hepatitis C 62 0.061
308
BRN004 Brain Edema 57 0.061
309
END040 Endogenous Depression 55 0.061
310
URM002 Uremia 50 0.061
311
ARG004 Argyria 28 0.061
312
P FRG001 Fragile X Syndrome 69 0.061
313
ANT024 Anthrax Disease 56 0.061
314
P OBS001 Obstructive Jaundice 49 0.061
315
ADG002 Audiogenic Seizures 25 0.061
316
AMN003 Amnestic Disorder 55 0.060
317
TLN003 Telangiectasis 53 0.059
318
CLF027 Cleft Palate, Isolated 67 0.059
319
IGR001 Ige Responsiveness, Atopic 61 0.059
320
GST023 Gastric Ulcer 53 0.059
321
P PRP029 Porphyria 58 0.058
322
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.058
323
CRN017 Coronary Thrombosis 45 0.058
324
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.058
325
c PSD066 Pseudohypoparathyroidism, Type Ib 51 0.058
326
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.058
327
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.058
328
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.058
329
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.058
330
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.058
331
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.058
332
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.058
333
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.058
334
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.058
335
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.058
336
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.058
337
c PSD104 Pseudohypoparathyroidism, Type Ii 31 0.058
338
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.058
339
P GST044 Gastritis 58 0.058
340
TRM010 Traumatic Brain Injury 54 0.058
341
PLG002 Plague 54 0.058
342
OST011 Osteomalacia 51 0.058
343
P HNT016 Huntington Disease 72 0.056
344
TRN015 Transient Cerebral Ischemia 62 0.056
345
c SVR001 Severe Acute Respiratory Syndrome 56 0.056
346
BYS001 Byssinosis 34 0.056
347
P SRC025 Sarcoidosis 1 72 0.056
348
RCK004 Rickets 70 0.056
349
KRT019 Keratitis, Hereditary 69 0.056
350
THY111 Thyroid Carcinoma, Familial Medullary 68 0.056
351
SPP010 Suppressor of Tumorigenicity 3 54 0.056
352
THY125 Thyroid Gland Medullary Carcinoma 52 0.056
353
HYP080 Hypogonadism 51 0.056
354
P RNL015 Renal Hypertension 47 0.056
355
HYP064 Hypogonadotropism 40 0.056
356
P HML002 Hemolytic Anemia 64 0.055
357
P CYS039 Cystic Kidney Disease 55 0.055
358
CHD001 Chediak-Higashi Syndrome 68 0.055
359
BRC012 Brucellosis 62 0.055
360
P ALP008 Alopecia 58 0.055
361
IRN002 Iron Metabolism Disease 58 0.055
362
c VRL010 Viral Hepatitis 56 0.055
363
RYN005 Raynaud Phenomenon 50 0.055
364
P HPT021 Hepatitis 69 0.053
365
P PNC044 Pancreatitis 61 0.053
366
P CRD132 Cardiac Conduction Defect 61 0.053
367
DPH001 Diphtheria 61 0.053
368
PSD014 Pseudopseudohypoparathyroidism 56 0.053
369
P INT068 Intestinal Disease 56 0.053
370
LMY002 Leiomyoma 52 0.053
371
P TRT010 Teratoma 52 0.053
372
OPD006 Opioid Addiction 49 0.053
373
WLL004 Wallerian Degeneration 40 0.053
374
c PRG020 Paragangliomas 3 36 0.053
375
ESP021 Esophageal Cancer 90 0.053
376
P MYC084 Mycobacterium Tuberculosis 1 69 0.053
377
c ATM011 Autoimmune Hepatitis 63 0.053
378
OST003 Osteonecrosis 62 0.053
379
CRD223 Cardiac Arrhythmia 61 0.053
380
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.053
381
P CHN012 Chondrosarcoma 57 0.053
382
P SML001 Small Cell Carcinoma 55 0.053
383
P PNC025 Panic Disorder 53 0.053
384
MYM001 Myoma 52 0.053
385
VTR007 Vitreoretinopathy 48 0.053
386
c HNT011 Huntington Disease-Like 3 37 0.053
387
P RSP003 Respiratory Failure 75 0.053
388
ACR007 Acromegaly 70 0.053
389
P DBT009 Diabetes Mellitus 66 0.053
390
NRM005 Neuromuscular Disease 62 0.053
391
P MLN007 Male Infertility 57 0.053
392
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.053
393
PHR003 Pharyngitis 56 0.053
394
MST005 Mastitis 55 0.053
395
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.051
396
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.051
397
MCC012 Mccune-Albright Syndrome 70 0.051
398
P SKN015 Skin Carcinoma 67 0.051
399
CLT003 Colitis 63 0.051
400
CYT008 Cytomegalovirus Infection 58 0.051
401
P EXN002 Exanthem 58 0.051
402
LYM027 Lymphopenia 58 0.051
403
P MTC069 Mitochondrial Disorders 57 0.051
404
P PLY041 Polymyositis 57 0.051
405
ATS010 Autosomal Recessive Disease 49 0.051
406
P END046 Endometritis 49 0.051
407
SYN036 Syncope 46 0.051
408
CHR178 Chromosomal Triplication 36 0.051
409
P LNG028 Long Qt Syndrome 68 0.051
410
P HYD006 Hydrocephalus 68 0.051
411
P DYS154 Dystonia 65 0.051
412
P CYS018 Cystitis 59 0.051
413
c CNG216 Congenital Hydrocephalus 55 0.051
414
SXL003 Sexual Disorder 49 0.051
415
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.051
416
SCR003 Secretory Diarrhea 36 0.051
417
P PYL005 Pyelonephritis 58 0.050
418
OCL052 Ocular Dominance 41 0.050
419
PLC006 Placental Choriocarcinoma 33 0.050
420
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 44 0.050
421
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.048
422
END041 Endometrial Adenocarcinoma 64 0.048
423
NTR005 Nutritional Deficiency Disease 61 0.048
424
INT007 Intermediate Coronary Syndrome 58 0.048
425
APH001 Aphthous Stomatitis 56 0.048
426
TRY001 Trypanosomiasis 50 0.048
427
P CHR012 Chronic Granulomatous Disease 69 0.048
428
P SPN046 Spinal Muscular Atrophy 65 0.048
429
NRF007 Neurofibroma 63 0.048
430
CRC021 Carcinosarcoma 62 0.048
431
P KDN017 Kidney Cancer 60 0.048
432
c HPT003 Hepatitis a 60 0.048
433
P RBL001 Rubella 56 0.048
434
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.048
435
HMS001 Hemosiderosis 54 0.048
436
FBR009 Fibrous Dysplasia 47 0.048
437
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.046
438
MCR013 Microphthalmia 62 0.046
439
STR067 Stroke, Ischemic 82 0.046
440
P PRK057 Parkinson Disease, Late-Onset 77 0.046
441
PNC129 Pancreatic Adenocarcinoma 69 0.046
442
P PRP019 Peripheral Nervous System Disease 64 0.046
443
P ADL010 Adult Respiratory Distress Syndrome 61 0.046
444
TRD006 Tardive Dyskinesia 58 0.046
445
GST050 Gastrointestinal System Disease 57 0.046
446
P FTL001 Fetal Alcohol Syndrome 56 0.046
447
DBT010 Diabetic Neuropathy 56 0.046
448
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.046
449
PNC001 Pancytopenia 54 0.046
450
P SCK005 Sickle Cell Disease 53 0.046
451
PRT029 Parathyroid Adenoma 52 0.046
452
P OPN001 Open-Angle Glaucoma 50 0.046
453
P GRF003 Graft-Versus-Host Disease 71 0.045
454
CHL065 Cholangiocarcinoma 68 0.045
455
SKN019 Skin Melanoma 68 0.045
456
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.045
457
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.045
458
P PLM034 Pulmonary Emphysema 55 0.045
459
c LKM070 Leukemia, Acute Monocytic 55 0.045
460
INT079 Intrahepatic Cholangiocarcinoma 54 0.045
461
CHC001 Chickenpox 53 0.045
462
NNL006 Non-Alcoholic Steatohepatitis 53 0.045
463
P LCT001 Lactic Acidosis 52 0.045
464
GNG005 Gangliocytoma 52 0.045
465
GNG002 Ganglioneuroma 52 0.045
466
OPT003 Opiate Dependence 50 0.045
467
P BNG032 Benign Mesothelioma 47 0.045
468
HDN002 Head Injury 47 0.045
469
ISL001 Islet Cell Tumor 47 0.045
470
FML075 Familial Isolated Hyperparathyroidism 44 0.045
471
c HYP243 Hyperparathyroidism 1 44 0.045
472
P HYP265 Hypotonia 43 0.045
473
P RRH023 Rare Hereditary Hemochromatosis 41 0.045
474
GNT029 Genetic Hypertension 39 0.045
475
AMN006 Aminoaciduria 39 0.045
476
WHP002 Whiplash 37 0.045
477
P FML187 Familial Hypertension 35 0.045
478
PSD119 Pseudohypoparathyroidism with Albright Hereditary Osteodystrophy 31 0.045
479
LYM133 Lymphoma, Hodgkin, Classic 70 0.044
480
ACT119 Acute Promyelocytic Leukemia 63 0.044
481
c GLC092 Glaucoma, Primary Open Angle 63 0.044
482
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.044
483
P CRN300 Coronary Heart Disease 1 59 0.044
484
BLR008 Bilirubin Metabolic Disorder 58 0.044
485
PLS011 Plasmacytoma 57 0.044
486
c LNG047 Long Qt Syndrome 2 57 0.044
487
PRM236 Primary Biliary Cholangitis 57 0.044
488
c PRD040 Periodontitis, Chronic 56 0.044
489
P PRM006 Primary Biliary Cirrhosis 54 0.044
490
PLV003 Pelvic Inflammatory Disease 54 0.044
491
P THY032 Thyroiditis 52 0.044
492
THR013 Thoracic Outlet Syndrome 49 0.044
493
PPL002 Papillary Carcinoma 47 0.044
494
c PRG106 Progressive Muscular Dystrophy 34 0.044
495
ADR007 Adrenoleukodystrophy 72 0.042
496
ADR022 Adrenomyeloneuropathy 39 0.042
497
P MYC026 Myoclonus Epilepsy 34 0.042
498
c MNN043 Meningioma, Familial 74 0.041
499
c ATS007 Autism Spectrum Disorder 69 0.041
500
EWN003 Ewing Sarcoma 69 0.041
501
P MTR014 Motor Neuron Disease 66 0.041
502
MNN042 Meningioma, Radiation-Induced 64 0.041
503
ORL011 Oral Cancer 62 0.041
504
P MYT002 Myotonic Dystrophy 52 0.041
505
CRY005 Cryptococcosis 51 0.041
506
CRD137 Cardiogenic Shock 50 0.041
507
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.041
508
THY128 Thyroid Tumor 49 0.041
509
LPD009 Lipid Storage Disease 49 0.041
510
c ACT042 Acute Pyelonephritis 44 0.041
511
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.041
512
SPN021 Spinal Meningioma 40 0.041
513
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.041
514
EXT006 Extrahepatic Cholestasis 38 0.041
515
TRP005 Trophoblastic Neoplasm 38 0.041
516
SCR001 Secretory Meningioma 38 0.041
517
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 37 0.041
518
c ATM022 Autoimmune Myocarditis 36 0.041
519
c PLY136 Polydactyly, Preaxial I 34 0.041
520
DFF012 Differentiating Neuroblastoma 32 0.041
521
OBN001 Ouabain Resistance 19 0.041
522
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.041
523
ART016 Aortic Aneurysm 71 0.041
524
P AGM001 Agammaglobulinemia 66 0.041
525
AND002 Androgen Insensitivity Syndrome 66 0.041
526
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.041
527
P ACR001 Aicardi-Goutieres Syndrome 63 0.041
528
P ESP024 Esophagitis 62 0.041
529
P CTR002 Cataract 62 0.041
530
P SYP003 Syphilis 59 0.041
531
P TRC086 Trichohepatoenteric Syndrome 1 57 0.041
532
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.041
533
CRH005 Crohn's Colitis 56 0.041
534
P PMP001 Pemphigus 56 0.041
535
PPL022 Papilloma 56 0.041
536
P ART021 Arteriosclerosis 56 0.041
537
PLY023 Polycystic Liver Disease 55 0.041
538
CHR100 Chronic Ulcer of Skin 53 0.041
539
c GLL024 Gallbladder Disease 1 53 0.041
540
MMM001 Mammary Paget's Disease 53 0.041
541
DYS073 Dysphagia 52 0.041
542
P MNC007 Monocytic Leukemia 52 0.041
543
PLC008 Placenta Disease 51 0.041
544
c BCT013 Bacterial Pneumonia 49 0.041
545
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.041
546
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.041
547
P PRC019 Precocious Puberty 48 0.041
548
P PRD021 Periodic Paralysis 47 0.041
549
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 47 0.041
550
INT052 Intestinal Volvulus 44 0.041
551
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.041
553
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.041
554
P RTT002 Rett Syndrome 81 0.038
555
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.038
556
SCK003 Sickle Cell Anemia 74 0.038
557
MSC157 Muscular Dystrophy, Duchenne Type 70 0.038
558
P OST001 Osteopetrosis 70 0.038
559
P DMN002 Dementia 68 0.038
560
P OLG002 Oligodendroglioma 67 0.038
561
BRR014 Barrett Esophagus 67 0.038
562
c CNG006 Congenital Hypothyroidism 65 0.038
563
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.038
564
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.038
565
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.038
566
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.038
567
P ALP009 Alopecia Areata 61 0.038
568
ETN001 Eating Disorder 61 0.038
569
ART140 Arteries, Anomalies of 60 0.038
570
GST045 Gastroenteritis 60 0.038
571
GST033 Gestational Diabetes 58 0.038
572
TNS005 Tonsillitis 58 0.038
573
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.038
574
SFT003 Soft Tissue Sarcoma 57 0.038
575
ACT200 Acute Monoblastic Leukemia 56 0.038
576
ATR057 Atrioventricular Block 56 0.038
577
c CNT035 Central Nervous System Disease 56 0.038
578
VSC003 Visceral Leishmaniasis 55 0.038
579
DCB001 Decubitus Ulcer 54 0.038
580
DNT012 Dental Caries 52 0.038
581
CRV040 Cervix Carcinoma 52 0.038
582
ASP003 Aseptic Meningitis 51 0.038
583
P AGG001 Aggressive Periodontitis 50 0.038
584
IGG001 Iga Glomerulonephritis 50 0.038
585
SBS004 Substance Dependence 48 0.038
586
ALB002 Albinism 48 0.038
587
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 38 0.038
588
STN013 Stenotrophomonas Maltophilia Infection 26 0.038
589
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.036
590
GST040 Gastric Adenocarcinoma 67 0.036
591
TBC004 Tobacco Addiction 65 0.036
592
c RHB024 Rhabdomyosarcoma 2 64 0.036
593
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.036
594
CYS010 Cystinosis 55 0.036
595
c SPN393 Spinal Muscular Atrophy, Type I 53 0.036
596
THY030 Thyroid Gland Disease 53 0.036
597
CYS036 Cystinosis, Nephropathic 53 0.036
598
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.036
599
P FNC004 Fanconi Syndrome 48 0.036
600
RSP021 Respiratory Allergy 45 0.036
601
MYT011 Myotonia 37 0.036
602
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 34 0.036
603
MYT026 Myotonia Atrophica 25 0.036
604
NRL016 Neural Tube Defects 83 0.034
605
c THR092 Thrombophilia Due to Thrombin Defect 74 0.034
606
ACR006 Aceruloplasminemia 74 0.034
607
c HMC039 Hemochromatosis, Type 1 73 0.034
608
CRB037 Cerebral Palsy 69 0.034
609
MYL005 Myelofibrosis 69 0.034
610
P KRB001 Krabbe Disease 68 0.034
611
P NRV007 Nervous System Disease 68 0.034
612
MYL031 Myeloproliferative Neoplasm 66 0.034
613
MST024 Mastocytosis, Cutaneous 65 0.034
614
MGK001 Megakaryocytic Leukemia 65 0.034
615
P THY023 Thymoma 64 0.034
616
c BRN108 Branchiootic Syndrome 1 62 0.034
617
P HMN010 Hemangioma 62 0.034
618
VRL011 Viral Infectious Disease 62 0.034
619
TYP007 Typhoid Fever 61 0.034
620
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.034
621
LKD001 Leukodystrophy 61 0.034
622
ANR040 Aneurysm 60 0.034
623
c LPM012 Lipomatosis, Multiple 60 0.034
624
P MLG056 Malignant Hyperthermia 60 0.034
625
P PGT001 Paget's Disease of Bone 59 0.034
626
P PRV006 Pervasive Developmental Disorder 58 0.034
627
ADR005 Adrenal Carcinoma 58 0.034
628
P AXN002 Axenfeld-Rieger Syndrome 58 0.034
629
BLM002 Bulimia Nervosa 56 0.034
630
HRT012 Heart Valve Disease 56 0.034
631
c THY107 Thymoma, Familial 55 0.034
632
P CHL066 Cholangitis 53 0.034
633
NRT004 Neuritis 52 0.034
634
QDR001 Quadriplegia 51 0.034
635
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 51 0.034
636
c SVR005 Severe Pre-Eclampsia 50 0.034
637
c PTT057 Pituitary Adenoma 4, Acth-Secreting 50 0.034
638
PST048 Postural Orthostatic Tachycardia Syndrome 49 0.034
639
CLC006 Calcinosis 48 0.034
640
GRW007 Growth Hormone Deficiency 48 0.034
641
PLP001 Pulpitis 48 0.034
642
DRG003 Drug Dependence 48 0.034
643
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 47 0.034
644
ORL015 Oral Squamous Cell Carcinoma 44 0.034
645
P RRT020 Rare Tumor 43 0.034
646
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.034
647
PLM005 Pleomorphic Lipoma 41 0.034
648
P ACT244 Acth-Independent Cushing Syndrome 40 0.034
649
AML001 Amelanotic Melanoma 38 0.034
650
P LTH003 Lethal Congenital Contracture Syndrome 38 0.034
651
GST039 Gastroduodenitis 34 0.034
652
BCL014 B-Cell Growth Factor 34 0.034
653
ALR002 Al-Raqad Syndrome 32 0.034
654
CHL079 Children's Interstitial Lung Disease 27 0.034
655
PRX085 Preaxial Hallucal Polydactyly 27 0.034
656
c ATS372 Autism 7 19 0.034
657
PLT016 Platelet Adenylate Cyclase Activity 17 0.034
658
NRN046 Neuronal Tumor 17 0.034
659
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.029
660
PFF001 Pfeiffer Syndrome 79 0.029
661
KPS004 Kaposi Sarcoma 75 0.029
662
PHN003 Phenylketonuria 73 0.029
663
c NRF024 Neurofibromatosis, Type I 72 0.029
664
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.029
665
P INF038 Influenza 69 0.029
666
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.029
667
c BSL007 Basal Cell Carcinoma 68 0.029
668
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 67 0.029
669
c ART101 Aortic Valve Disease 2 67 0.029
670
P PRS038 Personality Disorder 66 0.029
671
DSS008 Disease of Mental Health 66 0.029
672
P VNW001 Von Willebrand's Disease 64 0.029
673
P TST021 Testicular Germ Cell Tumor 63 0.029
674
PCK003 Pick Disease of Brain 63 0.029
675
BLD131 Bladder Urothelial Carcinoma 62 0.029
676
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 62 0.029
677
CTN007 Cutaneous Leishmaniasis 61 0.029
678
P EPN002 Ependymoma 61 0.029
679
P CHR285 Chronic Myelomonocytic Leukemia 60 0.029
680
P BRN019 Bernard-Soulier Syndrome 60 0.029
681
ALC006 Alcoholic Hepatitis 60 0.029
682
P WRD001 Waardenburg's Syndrome 60 0.029
683
BRN002 Bronchiolitis 60 0.029
684
c DWL002 Dowling-Degos Disease 1 59 0.029
685
P MLT074 Multiple Endocrine Neoplasia 59 0.029
686
c MST023 Mesothelioma, Malignant 59 0.029
687
P OCL002 Oculocutaneous Albinism 58 0.029
688
CNT047 Contact Dermatitis 58 0.029
689
QFV001 Q Fever 58 0.029
690
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.029
691
LMY014 Leiomyoma, Uterine 57 0.029
692
TRN018 Transitional Cell Carcinoma 57 0.029
693
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.029
694
DFF005 Diffuse Large B-Cell Lymphoma 56 0.029
695
P ANT006 Antiphospholipid Syndrome 56 0.029
696
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 56 0.029
697
P PTT014 Pitt-Hopkins Syndrome 55 0.029
698
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.029
699
SLC006 Silicosis 55 0.029
700
P LCH002 Lichen Planus 55 0.029
701
c RBN021 Rubinstein-Taybi Syndrome 1 55 0.029
702
CLN019 Colonic Disease 55 0.029
703
OCL022 Ocular Melanoma 54 0.029
704
HMT018 Hematopoietic Stem Cell Transplantation 54 0.029
705
P BRC006 Brachydactyly 54 0.029
706
TXC002 Toxic Encephalopathy 54 0.029
707
ECH003 Echinococcosis 54 0.029
708
P HMR003 Hemorrhagic Disease 54 0.029
709
DFF036 Differentiated Thyroid Carcinoma 53 0.029
710
SKN022 Skin Squamous Cell Carcinoma 53 0.029
711
NPH003 Nephrocalcinosis 52 0.029
712
HYP014 Hyperuricemia 52 0.029
713
P SCL048 Sclerosteosis 52 0.029
714
GSG001 Gas Gangrene 52 0.029
715
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 51 0.029
716
SCH012 Schizoaffective Disorder 50 0.029
717
P END047 Endophthalmitis 50 0.029
718
PRT018 Portal Vein Thrombosis 50 0.029
719
MTC005 Mitochondrial Metabolism Disease 50 0.029
720
P LNG035 Lung Large Cell Carcinoma 50 0.029
721
RFR010 Refractory Anemia 50 0.029
722
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 50 0.029
723
P LPM005 Lipomatosis 49 0.029
724
BHV002 Behavioral Variant of Frontotemporal Dementia 49 0.029
725
P CRV031 Cervical Adenocarcinoma 49 0.029
726
HPT014 Hepatorenal Syndrome 49 0.029
727
ACR013 Acrodysostosis 48 0.029
728
c BNG030 Benign Ependymoma 48 0.029
729
GLC106 Glucocorticoid Resistance, Generalized 48 0.029
730
P OLV001 Olivopontocerebellar Atrophy 48 0.029
731
HYP025 Hyperphosphatemia 47 0.029
732
CRB008 Cerebral Atherosclerosis 47 0.029
733
P BNG026 Benign Neonatal Seizures 47 0.029
734
CRY014 Cryptococcal Meningitis 46 0.029
735
NDL007 Nodular Goiter 46 0.029
736
P HYP776 Hyperparathyroidism, Neonatal Severe 46 0.029
737
MCR018 Microcytic Anemia 46 0.029
738
ASP007 Aspiration Pneumonia 46 0.029
739
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.029
740
P GNT008 Giant Cell Tumor 45 0.029
741
c SCH079 Schizophrenia 1 44 0.029
742
OBS082 Obstructive Nephropathy 44 0.029
743
ASB001 Asbestosis 44 0.029
744
IDP091 Idiopathic Nephrotic Syndrome 43 0.029
745
FLL031 Follicular Adenoma 43 0.029
746
SPN050 Spinocerebellar Degeneration 43 0.029
747
c CRN243 Carney Complex, Type 1 43 0.029
748
MCR017 Macrocytic Anemia 41 0.029
749
CRB086 Cerebral Aneurysms 41 0.029
750
PNM005 Pneumonic Plague 40 0.029
751
P TST026 Testicular Germ Cell Cancer 40 0.029
752
HYP141 Hyperphenylalaninemia 40 0.029
753
ACN019 Acanthamoeba Keratitis 40 0.029
754
LPM010 Lipomatosis, Multiple Symmetric 39 0.029
755
NRF003 Neurofibrosarcoma 39 0.029
756
OCL010 Ocular Hypotension 38 0.029
757
P CRB059 Cerebellar Degeneration 38 0.029
758
P SRT003 Sertoli-Leydig Cell Tumor 38 0.029
759
MLN003 Melancholia 38 0.029
760
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.029
761
ALC005 Alcoholic Pancreatitis 37 0.029
762
GRM010 Germ Cells Tumors 35 0.029
763
CRV030 Cervical Adenitis 34 0.029
764
PLM011 Plummer's Disease 34 0.029
765
c GLY097 Glycogen Storage Disease Ixb 33 0.029
766
c HRD198 Hereditary Dystonia 32 0.029
768
c PRG019 Paragangliomas 2 30 0.029
769
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.029
770
HGH001 High Pressure Neurological Syndrome 30 0.029
771
c SCH064 Schizophrenia 10 29 0.029
773
ACT162 Acute Sensory Ataxic Neuropathy 27 0.029
774
c ATS376 Autism 15 27 0.029
775
ASB003 Asbestos Intoxication 26 0.029
776
URT049 Urate Oxidase, Pseudogene 26 0.029
777
ANS017 Anosmia, Isolated Congenital 24 0.029
778
c RNG021 Ring Chromosome 5 24 0.029
779
SCN001 Secondary Hyperparathyroidism of Renal Origin 23 0.029
780
TRC123 Trichohepatoneurodevelopmental Syndrome 23 0.029
781
ACR079 Acrodysostosis with Multiple Hormone Resistance 20 0.029
782
MST022 Masticatory Muscles, Hypertrophy of 19 0.029
783
MYP026 Myopathy - Thyrotoxic 17 0.029
784
c PGM012 Pigmented Nodular Adrenocortical Disease, Primary, 3 17 0.029
785
MTR086 Motor Stereotypies 16 0.029
786
NVL002 Novelty Seeking Personality Trait 16 0.029
787
c RTN181 Retinitis Pigmentosa 2, X-Linked 16 0.029
788
NCL008 Nuclear Ribonucleic Acid 16 0.029
789
FRC013 Fructose Utilization 15 0.029
790
PRP074 Peripheral Resistance to Thyroid Hormones 15 0.029
791
c ANT081 Antigen Defined by Monoclonal Antibody T87 13 0.029
792
EPT028 Epithelial Basolateral Chloride Conductance Regulator, Rabbit, Homolog of 11 0.029
Content
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