Search results for cyclic amp

807 hits were found for cyclic amp

# Family MCID Name MIFTS Score
1
CHL014 Cholera 59 0.641
2
PRT037 Pertussis 65 0.502
3
P NRB001 Neuroblastoma 72 0.401
4
P GLM045 Glioma 63 0.324
5
GLL048 Glial Tumor 45 0.323
6
P PHC003 Pheochromocytoma 71 0.264
7
ADR040 Adrenal Gland Pheochromocytoma 46 0.264
8
P NTR004 Neutropenia 63 0.243
9
BNR002 Bone Resorption Disease 48 0.239
10
P HYP069 Hyperparathyroidism 63 0.233
11
48X005 48,xyyy 39 0.208
12
HLX001 Helix Syndrome 47 0.203
13
c PRM005 Primary Hyperparathyroidism 58 0.203
14
HYP266 Hypoxia 57 0.192
15
P AST007 Astrocytoma 51 0.190
16
OST159 Osteogenic Sarcoma 66 0.182
17
HYP066 Hyperglycemia 61 0.180
18
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.174
19
FTT001 Fatty Liver Disease 61 0.172
20
CHR074 Choriocarcinoma 47 0.171
21
P PSR002 Psoriasis 62 0.167
22
PST011 Pustulosis of Palm and Sole 52 0.165
23
INS024 Insulin-Like Growth Factor I 79 0.162
24
P LKM002 Leukemia 68 0.161
25
ADN018 Adenoma 59 0.161
26
PTT037 Pituitary Tumors 44 0.159
27
CYS001 Cystic Fibrosis 81 0.159
28
P VSC007 Vascular Disease 63 0.158
29
c MGR028 Migraine with or Without Aura 1 67 0.158
30
HYP056 Hypoglycemia 66 0.157
31
CYT002 Cytokine Deficiency 42 0.157
32
ISC004 Ischemia 58 0.156
33
ANX004 Anoxia 40 0.156
34
P CLR023 Colorectal Cancer 99 0.152
35
CNG034 Congestive Heart Failure 69 0.150
36
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.148
37
P HYP086 Hypothyroidism 69 0.145
38
P RHM011 Rheumatoid Arthritis 80 0.144
39
IMP005 Impotence 52 0.141
40
P HYP076 Hyperthyroidism 55 0.140
41
P LVR013 Liver Disease 68 0.139
42
P HRP006 Herpes Simplex 65 0.137
43
ATM095 Autoimmune Disease 62 0.136
44
HRW001 Hair Whorl 36 0.134
45
GLB015 Glioblastoma Multiforme 75 0.133
46
P THR014 Thrombocytopenia 67 0.132
47
PPL052 Papillomatosis, Confluent and Reticulated 33 0.132
48
P BRS047 Breast Cancer 97 0.131
49
BCT022 Bacterial Infectious Disease 56 0.131
50
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.131
51
P OST002 Osteoporosis 74 0.130
52
P HRT032 Heart Disease 75 0.129
53
P SZR006 Seizure Disorder 56 0.129
54
VSL002 Visual Epilepsy 59 0.128
55
P PLM037 Pulmonary Hypertension 67 0.128
56
c HYP595 Hypertension, Essential 84 0.127
57
P KDN018 Kidney Disease 72 0.126
58
TRT001 Teratocarcinoma 45 0.125
59
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.125
60
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.125
61
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.125
62
c LKM005 Leukemia, T-Cell, Chronic 34 0.125
63
P DRM053 Dermatitis, Atopic 66 0.124
64
P HPT023 Hepatocellular Carcinoma 100 0.121
65
P RTN024 Retinoblastoma 73 0.121
66
c FML008 Familial Retinoblastoma 53 0.121
67
ALL026 Allergic Hypersensitivity Disease 62 0.120
68
P PSD015 Pseudohypoparathyroidism 56 0.119
69
PNG002 Pain Agnosia 51 0.119
70
DPR016 Depression 63 0.119
71
P END044 Endometriosis 63 0.118
72
ALL014 Allergic Encephalomyelitis 38 0.118
73
DRM006 Dermatitis 61 0.117
74
STM007 Stomatitis 50 0.117
75
LVR012 Liver Cirrhosis 62 0.117
76
LPD008 Lipid Metabolism Disorder 62 0.116
77
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.115
78
P PRS040 Prostate Cancer 97 0.115
79
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.115
80
P ADN016 Adenocarcinoma 64 0.115
81
c ACT073 Acute Leukemia 58 0.114
82
P MYL006 Myeloid Leukemia 60 0.113
83
P DRR001 Diarrhea 55 0.112
84
P LYM118 Lymphoma 68 0.111
85
P GRV001 Graves' Disease 55 0.111
86
MST004 Mast Cell Neoplasm 42 0.111
87
EXT007 Extracutaneous Mastocytoma 38 0.111
88
EMB004 Embryonal Carcinoma 56 0.111
89
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.111
90
P PLY014 Polycystic Kidney Disease 62 0.111
91
SPN186 Spinal Cord Injury 60 0.110
92
P MLN008 Melanoma 69 0.110
93
AST005 Asthma 76 0.109
94
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.109
95
P FBR017 Fibrosarcoma 56 0.108
96
TTN003 Tetanus 65 0.107
97
THY029 Thyroid Carcinoma 59 0.107
98
P MYP004 Myopathy 70 0.106
99
47X002 47,xyy 49 0.106
100
P DBT005 Diabetes Insipidus 55 0.105
101
P PLY011 Polycystic Ovary Syndrome 56 0.104
102
INS001 Insulinoma 60 0.104
103
P OVR042 Ovarian Cancer 88 0.103
104
P HYP024 Hypoparathyroidism 56 0.103
105
P LKM062 Leukemia, Acute Lymphoblastic 69 0.103
106
c SYS001 Systemic Lupus Erythematosus 86 0.102
107
P LNG032 Lung Cancer 98 0.102
108
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.100
109
CHL068 Cholestasis 61 0.100
110
HYP060 Hyperinsulinism 54 0.100
111
P ALZ034 Alzheimer Disease 88 0.100
112
HMN044 Human Immunodeficiency Virus Type 1 71 0.099
113
P PNC035 Pancreatic Cancer 84 0.099
114
c PRC016 Pre-Eclampsia 63 0.099
115
OCL069 Ocular Motor Apraxia 51 0.099
116
c ATR087 Atrial Standstill 1 75 0.098
117
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.097
118
ATH013 Atherosclerosis Susceptibility 65 0.097
119
P ENC018 Encephalopathy 61 0.096
120
MNT002 Mental Depression 58 0.096
121
RCK004 Rickets 68 0.095
122
P RHN004 Rhinitis 57 0.095
123
P TRM003 Tremor 54 0.092
124
P BPL003 Bipolar Disorder 56 0.092
125
c MJR024 Major Affective Disorder 9 41 0.092
126
c MJR022 Major Affective Disorder 8 38 0.092
127
PLY150 Polykaryocytosis Inducer 31 0.092
128
GLC003 Glucose Intolerance 54 0.091
129
PST092 Posttransplant Acute Limbic Encephalitis 29 0.091
130
P PRD008 Periodontitis 64 0.091
131
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.091
132
c HYP836 Hypercholesterolemia, Familial, 1 73 0.090
133
ALL006 Allergic Asthma 56 0.089
134
c PCH010 Pachyonychia Congenita 3 44 0.089
135
ALL003 Allergic Rhinitis 67 0.089
136
c HPT073 Hepatitis C Virus 72 0.088
137
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.088
138
CHL123 Chlamydia 59 0.087
139
P MSC005 Muscular Dystrophy 66 0.087
140
c SCN007 Secondary Hyperparathyroidism 51 0.087
141
c MLG068 Malignant Glioma 46 0.087
142
P BCL017 B-Cell Lymphoma 58 0.086
143
IMM167 Immune Deficiency Disease 78 0.086
144
P BLD134 Bladder Cancer 79 0.085
145
c MCR113 Microvascular Complications of Diabetes 3 52 0.085
146
c MCR120 Microvascular Complications of Diabetes 7 47 0.085
147
c MCR130 Microvascular Complications of Diabetes 6 41 0.085
148
c MCR133 Microvascular Complications of Diabetes 4 41 0.085
149
CRB004 Cerebral Artery Occlusion 45 0.085
150
LNG099 Lung Disease 60 0.085
151
P HYP061 Hypertrophic Cardiomyopathy 70 0.085
152
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.085
153
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.084
154
ERY051 Erythroleukemia, Familial 56 0.084
155
P MJR007 Major Affective Disorder 1 43 0.084
156
P MJR001 Major Depressive Disorder 68 0.083
157
GTR002 Goiter 53 0.083
158
TXC005 Toxic Shock Syndrome 62 0.083
159
c DLT002 Dilated Cardiomyopathy 79 0.083
160
P INF037 Inflammatory Bowel Disease 54 0.083
161
P HDC001 Headache 57 0.082
162
c LKM061 Leukemia, Acute Myeloid 84 0.082
163
P ART022 Arthritis 69 0.081
164
c ACT071 Acute Kidney Failure 60 0.081
165
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.081
166
P HYP750 Hypertriglyceridemia, Familial 62 0.081
167
P RTN016 Retinal Degeneration 53 0.080
168
P HYP098 Hypereosinophilic Syndrome 67 0.080
169
NTR046 Neutrophil Migration 50 0.080
170
STT001 Status Epilepticus 60 0.079
171
c NRF023 Neurofibromatosis, Type Ii 80 0.079
172
P LKM071 Leukemia, Chronic Lymphocytic 79 0.079
173
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.078
174
ANX010 Anxiety 73 0.078
175
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.078
176
LYM019 Lymphosarcoma 46 0.078
177
WTH001 Withdrawal Disorder 48 0.078
178
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.078
179
LPP008 Lipoprotein Quantitative Trait Locus 62 0.077
180
VCC001 Vaccinia 49 0.077
181
ADR016 Adrenal Cortical Carcinoma 48 0.077
182
ADR004 Adrenal Cortical Adenocarcinoma 39 0.077
183
CNN003 Conn's Syndrome 79 0.076
184
PPT005 Peptic Ulcer Disease 59 0.076
185
P INF032 Infertility 57 0.076
186
MYL069 Myeloma, Multiple 85 0.076
187
BRN024 Bronchitis 68 0.076
189
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.076
190
MSC007 Muscle Hypertrophy 64 0.076
191
SKN016 Skin Disease 63 0.075
192
END057 Endometrial Cancer 74 0.075
193
P LPS004 Lupus Erythematosus 61 0.075
194
CRB039 Cerebrovascular Disease 67 0.074
195
P CND004 Candidiasis 58 0.074
196
PLM010 Pulmonary Edema 54 0.074
197
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.074
198
BRN071 Brain Injury 49 0.074
199
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.074
200
WLF001 Wolff-Parkinson-White Syndrome 66 0.073
201
P PTT006 Pituitary Adenoma 55 0.073
202
P BND020 Bone Disease 59 0.072
203
P CHR345 Chronic Pain 44 0.072
204
HPT004 Hepatic Coma 45 0.072
205
P ADL017 Adult T-Cell Leukemia 56 0.072
206
P GLM040 Glioma Susceptibility 1 81 0.071
207
ANT024 Anthrax Disease 58 0.071
208
P MSC003 Muscular Atrophy 52 0.071
209
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
210
CLN015 Colon Adenocarcinoma 65 0.071
211
HYP005 Hypokalemia 55 0.071
212
P DDN001 Duodenal Ulcer 52 0.071
213
P TBR001 Tuberous Sclerosis 70 0.071
214
ALC007 Alcohol Dependence 66 0.071
215
c SCL052 Scleroderma, Familial Progressive 61 0.071
216
c SML038 Small Cell Cancer of the Lung 65 0.071
217
MSL001 Measles 62 0.071
218
P ECL001 Eclampsia 50 0.071
219
P MYC008 Myocarditis 59 0.070
220
P NRF002 Neurofibromatosis 56 0.070
221
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.070
222
DMY004 Demyelinating Disease 52 0.070
223
c ACT075 Acute Myocardial Infarction 57 0.069
224
END086 End Stage Renal Disease 51 0.069
225
CRV035 Cervical Cancer 76 0.069
226
c CHR684 Chronic Kidney Disease 70 0.069
227
c SVR001 Severe Acute Respiratory Syndrome 62 0.069
228
P CRN038 Carney Complex Variant 61 0.069
229
P ALC033 Alcohol Use Disorder 58 0.069
230
PLR008 Pleurisy 50 0.069
231
P MLT020 Multiple Sclerosis 72 0.069
232
ANV001 Anovulation 47 0.068
233
MLR004 Malaria 81 0.068
234
CRH001 Crohn's Disease 74 0.067
235
IRR002 Irritable Bowel Syndrome 65 0.067
236
SQM006 Squamous Cell Carcinoma 60 0.067
237
c TBR025 Tuberous Sclerosis 1 77 0.066
238
c GRV008 Graves Disease 1 56 0.066
239
BRC012 Brucellosis 64 0.066
240
BRS051 Breast Disease 58 0.066
241
P ATX030 Ataxia-Telangiectasia 82 0.066
242
P RHB003 Rhabdomyosarcoma 63 0.066
243
P SYS005 Systemic Scleroderma 68 0.066
244
P VSC011 Vasculitis 62 0.066
245
P MDL005 Medulloblastoma 77 0.065
246
LSH001 Leishmaniasis 63 0.065
247
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.065
248
SVR004 Severe Combined Immunodeficiency 73 0.065
249
ADL002 Adult Syndrome 70 0.065
250
P MCR115 Microvascular Complications of Diabetes 5 66 0.065
251
RNL077 Renal Fibrosis 47 0.065
252
CHG001 Chagas Disease 66 0.064
253
LYM017 Lyme Disease 64 0.064
254
MDD011 Mood Disorder 62 0.064
255
DYS015 Dysentery 52 0.064
256
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.064
257
P NRP001 Neuropathy 56 0.063
258
MYL009 Myelodysplastic Syndrome 70 0.063
259
c HPT001 Hepatitis C 62 0.063
260
c ACT027 Acute Pancreatitis 60 0.063
261
c HPT016 Hepatitis B 59 0.063
262
URL001 Urolithiasis 45 0.063
263
P KLZ004 Kala-Azar 1 41 0.063
264
P PNM007 Pneumonia 68 0.063
265
P CRD119 Cardiac Arrest 67 0.063
266
ANG054 Angina Pectoris 66 0.063
267
P MNN013 Meningitis 66 0.063
268
PLG002 Plague 63 0.063
269
P LNG064 Lung Cancer Susceptibility 3 78 0.063
270
P PLM036 Pulmonary Fibrosis 65 0.063
271
ACQ007 Acquired Immunodeficiency Syndrome 60 0.062
272
URT010 Ureteral Obstruction 45 0.062
273
c PSD117 Pseudohypoparathyroidism, Type Ic 38 0.062
274
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.061
275
P GST053 Gastric Cancer 83 0.061
276
P ATS364 Autism 70 0.061
277
P MYS003 Myasthenia Gravis 68 0.061
278
P LTR001 Lateral Sclerosis 54 0.061
279
MTB004 Metabolic Acidosis 50 0.061
280
MRP001 Morphine Dependence 41 0.061
281
PLM001 Pulmonary Tuberculosis 69 0.061
282
P NPH012 Nephrotic Syndrome 60 0.061
283
AGN016 Aging 56 0.061
284
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.061
285
SPL018 Splenomegaly 48 0.061
286
P MYC033 Myoclonus 46 0.061
287
LYD001 Leydig Cell Tumor 45 0.061
288
CRT015 Carotid Artery Occlusion 45 0.061
289
HMP009 Haemophilus Influenzae 43 0.061
290
P SCH015 Schizophrenia 74 0.060
291
DWN001 Down Syndrome 70 0.060
292
P INT143 Interstitial Cystitis 61 0.060
293
TLN003 Telangiectasis 52 0.060
294
GT001 Gout 64 0.060
295
P GLY013 Glycogen Storage Disease 60 0.060
296
P DBT009 Diabetes Mellitus 64 0.059
297
HPT019 Hepatic Encephalopathy 60 0.059
298
P DNG005 Dengue Virus 59 0.059
299
NRL005 Neurilemmoma 60 0.059
300
P END033 Endocarditis 57 0.059
301
BRN004 Brain Edema 56 0.059
302
END040 Endogenous Depression 55 0.059
303
GST023 Gastric Ulcer 53 0.059
304
HYP080 Hypogonadism 50 0.059
305
URM002 Uremia 49 0.059
306
ARG004 Argyria 27 0.059
307
P FRG001 Fragile X Syndrome 70 0.058
308
P OBS001 Obstructive Jaundice 50 0.058
309
ADG002 Audiogenic Seizures 25 0.058
310
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.057
311
c PNS012 Paine Syndrome 61 0.057
312
P ENC004 Encephalitis 61 0.057
313
P GST044 Gastritis 56 0.057
314
AMN003 Amnestic Disorder 54 0.057
315
P ATR011 Atrial Fibrillation 66 0.057
316
SRC014 Sarcoma 65 0.056
317
CLF027 Cleft Palate, Isolated 64 0.056
318
IGR001 Ige Responsiveness, Atopic 59 0.056
319
SPN035 Spindle Cell Sarcoma 53 0.056
320
OST012 Osteoarthritis 78 0.056
321
c LKM063 Leukemia, Chronic Myeloid 72 0.056
322
DFC004 Deficiency Anemia 70 0.056
323
P PRP029 Porphyria 62 0.056
324
CRN017 Coronary Thrombosis 47 0.056
325
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.056
326
c PSD066 Pseudohypoparathyroidism, Type Ib 55 0.056
327
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.056
328
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.056
329
c PSD104 Pseudohypoparathyroidism, Type Ii 31 0.056
330
P SRC025 Sarcoidosis 1 70 0.055
331
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.055
332
OST011 Osteomalacia 52 0.055
333
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.055
334
P EPL164 Epilepsy 71 0.054
335
P ALP008 Alopecia 54 0.054
336
MDD018 Middle East Respiratory Syndrome 43 0.054
337
P HNT016 Huntington Disease 72 0.054
338
TRN015 Transient Cerebral Ischemia 63 0.054
339
BYS001 Byssinosis 28 0.054
340
THY111 Thyroid Carcinoma, Familial Medullary 67 0.053
341
KRT019 Keratitis, Hereditary 65 0.053
342
OST003 Osteonecrosis 61 0.053
343
P SPP010 Suppressor of Tumorigenicity 3 51 0.053
344
TRM010 Traumatic Brain Injury 51 0.053
345
THY125 Thyroid Gland Medullary Carcinoma 50 0.053
346
P RNL015 Renal Hypertension 47 0.053
347
P HML002 Hemolytic Anemia 63 0.053
348
P CYS039 Cystic Kidney Disease 54 0.053
349
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.052
350
CHD001 Chediak-Higashi Syndrome 66 0.052
351
IRN002 Iron Metabolism Disease 57 0.052
352
c VRL010 Viral Hepatitis 52 0.052
353
RYN005 Raynaud Phenomenon 47 0.052
354
P PNC044 Pancreatitis 61 0.051
355
DPH001 Diphtheria 60 0.051
356
CRD132 Cardiac Conduction Defect 58 0.051
357
P PYL005 Pyelonephritis 56 0.051
358
PSD014 Pseudopseudohypoparathyroidism 55 0.051
359
P INT068 Intestinal Disease 53 0.051
360
P TRT010 Teratoma 52 0.051
361
LMY002 Leiomyoma 52 0.051
362
OPD006 Opioid Addiction 48 0.051
363
WLL004 Wallerian Degeneration 39 0.051
364
c PRG020 Paragangliomas 3 39 0.051
365
ESP021 Esophageal Cancer 90 0.051
366
P MYC084 Mycobacterium Tuberculosis 1 68 0.051
367
c ATM011 Autoimmune Hepatitis 63 0.051
368
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.051
369
CLT003 Colitis 62 0.051
370
CRD223 Cardiac Arrhythmia 60 0.051
371
P EXN002 Exanthem 57 0.051
372
CYT008 Cytomegalovirus Infection 57 0.051
373
P CHN012 Chondrosarcoma 56 0.051
374
MYM001 Myoma 54 0.051
375
P PNC025 Panic Disorder 53 0.051
376
P SML001 Small Cell Carcinoma 52 0.051
377
P END046 Endometritis 49 0.051
378
P VTR007 Vitreoretinopathy 46 0.051
379
c HNT011 Huntington Disease-Like 3 38 0.051
380
P RSP003 Respiratory Failure 74 0.050
381
ACR007 Acromegaly 71 0.050
382
P MYC007 Myocardial Infarction 70 0.050
383
NRM005 Neuromuscular Disease 64 0.050
384
c ACT068 Acute Cystitis 63 0.050
385
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.050
386
PHR003 Pharyngitis 57 0.050
387
P MLN007 Male Infertility 55 0.050
388
MST005 Mastitis 53 0.050
389
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.049
390
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.049
391
MCC012 Mccune-Albright Syndrome 70 0.049
392
P SKN015 Skin Carcinoma 66 0.049
393
LYM027 Lymphopenia 58 0.049
394
P PLY041 Polymyositis 57 0.049
395
PLY023 Polycystic Liver Disease 57 0.049
396
P MTC069 Mitochondrial Disorders 56 0.049
397
ATS010 Autosomal Recessive Disease 48 0.049
398
SYN036 Syncope 45 0.049
399
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.049
400
CHR178 Chromosomal Triplication 35 0.049
401
P LNG028 Long Qt Syndrome 66 0.049
402
P HYD006 Hydrocephalus 66 0.049
403
P DYS154 Dystonia 65 0.049
404
END041 Endometrial Adenocarcinoma 63 0.049
405
P CYS018 Cystitis 59 0.049
406
TRY001 Trypanosomiasis 50 0.049
407
SXL003 Sexual Disorder 47 0.049
408
SCR003 Secretory Diarrhea 37 0.049
409
P CRD246 Cardiovascular System Disease 57 0.048
410
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.048
411
MCR013 Microphthalmia 57 0.048
412
OCL052 Ocular Dominance 42 0.048
413
PLC006 Placental Choriocarcinoma 36 0.048
414
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.046
415
P ADL010 Adult Respiratory Distress Syndrome 65 0.046
416
NTR005 Nutritional Deficiency Disease 62 0.046
417
P PRP019 Peripheral Nervous System Disease 58 0.046
418
APH001 Aphthous Stomatitis 57 0.046
419
GST050 Gastrointestinal System Disease 56 0.046
420
INT007 Intermediate Coronary Syndrome 55 0.046
421
P GRF003 Graft-Versus-Host Disease 72 0.046
422
P HPT021 Hepatitis 67 0.046
423
P CHR012 Chronic Granulomatous Disease 67 0.046
424
NRF007 Neurofibroma 64 0.046
425
c HPT003 Hepatitis a 62 0.046
426
P SPN046 Spinal Muscular Atrophy 62 0.046
427
CRC021 Carcinosarcoma 62 0.046
428
P KDN017 Kidney Cancer 60 0.046
429
P RBL001 Rubella 59 0.046
430
c LKM070 Leukemia, Acute Monocytic 57 0.046
431
HMS001 Hemosiderosis 54 0.046
432
FBR009 Fibrous Dysplasia 48 0.046
433
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.045
434
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.045
435
STR067 Stroke, Ischemic 81 0.044
436
P PRK057 Parkinson Disease, Late-Onset 78 0.044
437
PNC129 Pancreatic Adenocarcinoma 68 0.044
438
ANR007 Anorexia Nervosa 63 0.044
439
P FTL001 Fetal Alcohol Syndrome 57 0.044
440
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.044
441
CHR100 Chronic Ulcer of Skin 55 0.044
442
TRD006 Tardive Dyskinesia 54 0.044
443
DBT010 Diabetic Neuropathy 54 0.044
444
PNC001 Pancytopenia 54 0.044
445
PRT029 Parathyroid Adenoma 50 0.044
446
P SCK005 Sickle Cell Disease 50 0.044
447
P OPN001 Open-Angle Glaucoma 49 0.044
448
BCK006 Back Pain 42 0.044
449
GST040 Gastric Adenocarcinoma 70 0.043
450
CHL065 Cholangiocarcinoma 68 0.043
451
SKN019 Skin Melanoma 68 0.043
452
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.043
453
CHC001 Chickenpox 60 0.043
454
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.043
455
ISL001 Islet Cell Tumor 56 0.043
456
NPH009 Nephrolithiasis 55 0.043
457
P PLM034 Pulmonary Emphysema 55 0.043
458
GNG005 Gangliocytoma 55 0.043
459
GNG002 Ganglioneuroma 52 0.043
460
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.043
461
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.043
462
c HYP243 Hyperparathyroidism 1 51 0.043
463
P LCT001 Lactic Acidosis 51 0.043
464
INT079 Intrahepatic Cholangiocarcinoma 51 0.043
465
OPT003 Opiate Dependence 50 0.043
466
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.043
467
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.043
468
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.043
469
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.043
470
P BNG032 Benign Mesothelioma 46 0.043
471
HDN002 Head Injury 46 0.043
472
c ACT042 Acute Pyelonephritis 46 0.043
473
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.043
474
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.043
475
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.043
476
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.043
477
P HYP265 Hypotonia 43 0.043
478
P RRH023 Rare Hereditary Hemochromatosis 41 0.043
479
AMN006 Aminoaciduria 38 0.043
480
P FML187 Familial Hypertension 37 0.043
481
WHP002 Whiplash 36 0.043
482
c ATM022 Autoimmune Myocarditis 35 0.043
483
OTT002 Otitis Media 72 0.042
484
LYM133 Lymphoma, Hodgkin, Classic 69 0.042
485
ACT119 Acute Promyelocytic Leukemia 63 0.042
486
c GLC092 Glaucoma, Primary Open Angle 62 0.042
487
P ESP024 Esophagitis 62 0.042
488
P PRM006 Primary Biliary Cirrhosis 62 0.042
489
P CTR002 Cataract 60 0.042
490
GST045 Gastroenteritis 59 0.042
491
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.042
492
c LNG047 Long Qt Syndrome 2 58 0.042
493
PST028 Post-Traumatic Stress Disorder 58 0.042
494
BLR008 Bilirubin Metabolic Disorder 57 0.042
495
PLS011 Plasmacytoma 56 0.042
496
c PRD040 Periodontitis, Chronic 53 0.042
497
P THY032 Thyroiditis 52 0.042
498
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 49 0.042
499
PPL002 Papillary Carcinoma 47 0.042
500
ACT084 Acute Stress Disorder 47 0.042
501
c PRG106 Progressive Muscular Dystrophy 33 0.042
502
ADR007 Adrenoleukodystrophy 75 0.040
503
c RHB024 Rhabdomyosarcoma 2 67 0.040
504
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.040
505
ADR022 Adrenomyeloneuropathy 38 0.040
506
P MYC026 Myoclonus Epilepsy 35 0.040
507
c MNN043 Meningioma, Familial 74 0.039
508
EWN003 Ewing Sarcoma 69 0.039
509
c ATS007 Autism Spectrum Disorder 67 0.039
510
P MTR014 Motor Neuron Disease 65 0.039
511
c FNC043 Fanconi Anemia, Complementation Group E 62 0.039
512
MNN042 Meningioma, Radiation-Induced 62 0.039
513
ORL011 Oral Cancer 60 0.039
514
CRY005 Cryptococcosis 58 0.039
515
DSS008 Disease of Mental Health 58 0.039
516
PNM005 Pneumonic Plague 51 0.039
517
SPN021 Spinal Meningioma 50 0.039
518
P MYT002 Myotonic Dystrophy 49 0.039
519
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.039
520
THY128 Thyroid Tumor 47 0.039
521
CRD137 Cardiogenic Shock 47 0.039
522
LPD009 Lipid Storage Disease 46 0.039
523
SCR001 Secretory Meningioma 41 0.039
524
EXT006 Extrahepatic Cholestasis 39 0.039
525
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.039
526
TRP005 Trophoblastic Neoplasm 38 0.039
527
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.039
528
c PLY136 Polydactyly, Preaxial I 33 0.039
529
DFF012 Differentiating Neuroblastoma 28 0.039
530
OBN001 Ouabain Resistance 18 0.039
531
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.039
532
ART016 Aortic Aneurysm 69 0.039
533
AND002 Androgen Insensitivity Syndrome 66 0.039
534
P NRV007 Nervous System Disease 66 0.039
535
P AGM001 Agammaglobulinemia 65 0.039
536
P CRN300 Coronary Heart Disease 1 63 0.039
537
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.039
538
P TRC086 Trichohepatoenteric Syndrome 1 62 0.039
539
P ACR001 Aicardi-Goutieres Syndrome 62 0.039
540
P SYP003 Syphilis 58 0.039
541
TNS005 Tonsillitis 57 0.039
542
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.039
543
SFT003 Soft Tissue Sarcoma 56 0.039
544
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.039
545
PLV003 Pelvic Inflammatory Disease 55 0.039
546
VSC003 Visceral Leishmaniasis 55 0.039
547
P PMP001 Pemphigus 54 0.039
548
THR013 Thoracic Outlet Syndrome 54 0.039
549
P ART021 Arteriosclerosis 54 0.039
550
PPL022 Papilloma 54 0.039
551
MMM001 Mammary Paget's Disease 53 0.039
552
P MNC007 Monocytic Leukemia 53 0.039
553
CRH005 Crohn's Colitis 53 0.039
554
c GLL024 Gallbladder Disease 1 53 0.039
555
ASP003 Aseptic Meningitis 51 0.039
556
P AGG001 Aggressive Periodontitis 50 0.039
557
PLC008 Placenta Disease 50 0.039
558
DYS073 Dysphagia 50 0.039
559
VLV047 Volvulus of Midgut 49 0.039
560
c BCT013 Bacterial Pneumonia 48 0.039
561
P PRC019 Precocious Puberty 46 0.039
562
P PRD021 Periodic Paralysis 45 0.039
563
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.039
565
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.039
566
KPS004 Kaposi Sarcoma 75 0.036
567
SCK003 Sickle Cell Anemia 74 0.036
568
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.036
569
MSC157 Muscular Dystrophy, Duchenne Type 72 0.036
570
PRP027 Peripheral Vascular Disease 71 0.036
571
P OST001 Osteopetrosis 70 0.036
572
P OLG002 Oligodendroglioma 67 0.036
573
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.036
574
BRR014 Barrett Esophagus 65 0.036
575
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.036
576
c CNG006 Congenital Hypothyroidism 64 0.036
577
TYP007 Typhoid Fever 63 0.036
578
GST033 Gestational Diabetes 61 0.036
579
DCB001 Decubitus Ulcer 61 0.036
580
P ALP009 Alopecia Areata 60 0.036
581
ETN001 Eating Disorder 60 0.036
582
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.036
583
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.036
584
ATR057 Atrioventricular Block 55 0.036
585
DNT012 Dental Caries 53 0.036
586
c CNT035 Central Nervous System Disease 52 0.036
587
NRT004 Neuritis 52 0.036
588
P HYP730 Hypogonadotropic Hypogonadism 52 0.036
589
ACT200 Acute Monoblastic Leukemia 52 0.036
590
CRV040 Cervix Carcinoma 51 0.036
591
PLP001 Pulpitis 49 0.036
592
MNN009 Meningoencephalitis 49 0.036
593
SBS004 Substance Dependence 48 0.036
594
IGG001 Iga Glomerulonephritis 48 0.036
595
ALB002 Albinism 46 0.036
596
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.036
597
STN013 Stenotrophomonas Maltophilia Infection 25 0.036
598
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.035
599
P PRS038 Personality Disorder 65 0.035
600
TBC004 Tobacco Addiction 64 0.035
601
CYS010 Cystinosis 59 0.035
602
THY030 Thyroid Gland Disease 52 0.035
603
c SPN393 Spinal Muscular Atrophy, Type I 52 0.035
604
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.035
605
P FNC004 Fanconi Syndrome 50 0.035
606
RSP021 Respiratory Allergy 45 0.035
607
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 37 0.035
608
MYT011 Myotonia 34 0.035
609
URT049 Urate Oxidase, Pseudogene 25 0.035
610
NRL016 Neural Tube Defects 82 0.033
611
P RTT002 Rett Syndrome 80 0.033
612
c HMC039 Hemochromatosis, Type 1 74 0.033
613
c THR092 Thrombophilia Due to Thrombin Defect 73 0.033
614
MYL005 Myelofibrosis 70 0.033
615
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.033
616
P KRB001 Krabbe Disease 69 0.033
617
CRB037 Cerebral Palsy 69 0.033
618
P INF038 Influenza 68 0.033
619
P MLG056 Malignant Hyperthermia 67 0.033
620
P DMN002 Dementia 66 0.033
621
MYL031 Myeloproliferative Neoplasm 66 0.033
622
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.033
623
P THY023 Thymoma 65 0.033
624
MGK001 Megakaryocytic Leukemia 64 0.033
625
c BRN108 Branchiootic Syndrome 1 62 0.033
626
ALC006 Alcoholic Hepatitis 61 0.033
627
VRL011 Viral Infectious Disease 61 0.033
628
P HMN010 Hemangioma 61 0.033
629
c LPM012 Lipomatosis, Multiple 60 0.033
630
QFV001 Q Fever 60 0.033
631
SPP011 Suppression of Tumorigenicity 12 59 0.033
632
P AXN002 Axenfeld-Rieger Syndrome 59 0.033
633
P LKD001 Leukodystrophy 59 0.033
634
BRN002 Bronchiolitis 59 0.033
635
ANR040 Aneurysm 59 0.033
636
P PGT001 Paget's Disease of Bone 58 0.033
637
CNT047 Contact Dermatitis 58 0.033
638
ADR005 Adrenal Carcinoma 58 0.033
639
c DWL002 Dowling-Degos Disease 1 58 0.033
640
P PLV020 Pelvic Organ Prolapse 57 0.033
641
BLM002 Bulimia Nervosa 57 0.033
642
P PRV006 Pervasive Developmental Disorder 57 0.033
643
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.033
644
SLC006 Silicosis 56 0.033
645
P LCH002 Lichen Planus 53 0.033
646
HRT012 Heart Valve Disease 53 0.033
647
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 53 0.033
648
ART140 Arteries, Anomalies of 52 0.033
649
c THY107 Thymoma, Familial 52 0.033
650
PLS009 Plasma Cell Neoplasm 51 0.033
651
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.033
652
P CHL066 Cholangitis 51 0.033
653
CHR005 Chorioamnionitis 51 0.033
654
c SVR005 Severe Pre-Eclampsia 50 0.033
655
QDR001 Quadriplegia 48 0.033
656
CLC006 Calcinosis 48 0.033
657
RFR010 Refractory Anemia 48 0.033
658
DRG003 Drug Dependence 47 0.033
659
RTN020 Retinal Vascular Disease 46 0.033
660
GRW007 Growth Hormone Deficiency 46 0.033
661
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.033
662
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.033
663
ORL015 Oral Squamous Cell Carcinoma 43 0.033
664
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.033
665
P ACT244 Acth-Independent Cushing Syndrome 42 0.033
666
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.033
667
P RRT020 Rare Tumor 41 0.033
668
P LTH003 Lethal Congenital Contracture Syndrome 40 0.033
669
PLM005 Pleomorphic Lipoma 40 0.033
670
AML001 Amelanotic Melanoma 39 0.033
671
BCL014 B-Cell Growth Factor 35 0.033
672
ALR002 Al-Raqad Syndrome 33 0.033
673
GST039 Gastroduodenitis 31 0.033
674
PRX085 Preaxial Hallucal Polydactyly 28 0.033
675
c ATS372 Autism 7 19 0.033
676
NRN046 Neuronal Tumor 18 0.033
677
PLT016 Platelet Adenylate Cyclase Activity 16 0.033
678
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.028
679
PFF001 Pfeiffer Syndrome 79 0.028
680
c NRF024 Neurofibromatosis, Type I 77 0.028
681
PHN003 Phenylketonuria 75 0.028
682
P CNR004 Cone-Rod Dystrophy 2 73 0.028
683
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.028
684
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.028
685
MST024 Mastocytosis, Cutaneous 69 0.028
686
c BSL007 Basal Cell Carcinoma 68 0.028
687
PCK003 Pick Disease of Brain 68 0.028
688
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 0.028
689
P VNW001 Von Willebrand's Disease 65 0.028
690
c ART101 Aortic Valve Disease 2 65 0.028
691
c DBT099 Diabetes Mellitus, Type I 65 0.028
692
P PTT014 Pitt-Hopkins Syndrome 63 0.028
693
CTN007 Cutaneous Leishmaniasis 62 0.028
694
BLD131 Bladder Urothelial Carcinoma 62 0.028
695
FBR086 Fibrolamellar Carcinoma 61 0.028
696
P TST021 Testicular Germ Cell Tumor 60 0.028
697
P BNG030 Benign Ependymoma 60 0.028
698
P OCL002 Oculocutaneous Albinism 60 0.028
699
P CHR285 Chronic Myelomonocytic Leukemia 60 0.028
700
c OTP006 Otopalatodigital Syndrome, Type I 60 0.028
701
P BRN019 Bernard-Soulier Syndrome 60 0.028
702
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.028
703
P WRD001 Waardenburg's Syndrome 59 0.028
704
c MST023 Mesothelioma, Malignant 57 0.028
705
c RBN021 Rubinstein-Taybi Syndrome 1 57 0.028
706
SKN022 Skin Squamous Cell Carcinoma 57 0.028
707
P MLT074 Multiple Endocrine Neoplasia 56 0.028
708
TRN018 Transitional Cell Carcinoma 56 0.028
709
LMY014 Leiomyoma, Uterine 56 0.028
710
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 56 0.028
711
BRN012 Bronchiolitis Obliterans 55 0.028
712
DFF005 Diffuse Large B-Cell Lymphoma 55 0.028
713
P ANT006 Antiphospholipid Syndrome 55 0.028
714
P SCL048 Sclerosteosis 55 0.028
715
CLL010 Cellular Ependymoma 54 0.028
716
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.028
717
P LNG035 Lung Large Cell Carcinoma 54 0.028
718
WST005 West Nile Virus 54 0.028
719
P BRC006 Brachydactyly 53 0.028
720
P END047 Endophthalmitis 53 0.028
721
ECH003 Echinococcosis 53 0.028
722
INF034 Infective Endocarditis 53 0.028
723
P HMR003 Hemorrhagic Disease 53 0.028
724
GSG001 Gas Gangrene 53 0.028
725
TXC002 Toxic Encephalopathy 53 0.028
726
HYP014 Hyperuricemia 52 0.028
727
DFF036 Differentiated Thyroid Carcinoma 52 0.028
728
NPH003 Nephrocalcinosis 51 0.028
729
P OLV001 Olivopontocerebellar Atrophy 51 0.028
730
ACR013 Acrodysostosis 51 0.028
731
c VRL007 Viral Encephalitis 51 0.028
732
SCH012 Schizoaffective Disorder 50 0.028
733
HPT014 Hepatorenal Syndrome 50 0.028
734
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 50 0.028
735
PRT018 Portal Vein Thrombosis 50 0.028
736
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.028
737
OCL022 Ocular Melanoma 50 0.028
738
P BNG026 Benign Neonatal Seizures 49 0.028
739
CCN002 Cocaine Abuse 49 0.028
740
P CRV031 Cervical Adenocarcinoma 49 0.028
741
MTC005 Mitochondrial Metabolism Disease 49 0.028
742
ASP007 Aspiration Pneumonia 48 0.028
743
GLC106 Glucocorticoid Resistance, Generalized 48 0.028
744
HYP025 Hyperphosphatemia 48 0.028
745
MCR018 Microcytic Anemia 47 0.028
746
ASB001 Asbestosis 47 0.028
747
CLN019 Colonic Disease 47 0.028
748
NDL007 Nodular Goiter 47 0.028
749
P HYP776 Hyperparathyroidism, Neonatal Severe 47 0.028
750
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.028
751
P LPM005 Lipomatosis 46 0.028
752
c SCH079 Schizophrenia 1 46 0.028
753
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.028
754
c GLY097 Glycogen Storage Disease Ixb 44 0.028
755
CRB008 Cerebral Atherosclerosis 44 0.028
756
P BNG095 Benign Giant Cell Tumor 44 0.028
757
BCT021 Bacterial Sepsis 44 0.028
758
MCR017 Macrocytic Anemia 44 0.028
759
P TST026 Testicular Germ Cell Cancer 43 0.028
760
c CRN243 Carney Complex, Type 1 43 0.028
761
NRF003 Neurofibrosarcoma 43 0.028
762
OBS082 Obstructive Nephropathy 42 0.028
763
IDP091 Idiopathic Nephrotic Syndrome 42 0.028
764
LPM010 Lipomatosis, Multiple Symmetric 42 0.028
765
SPN050 Spinocerebellar Degeneration 42 0.028
766
P FNC034 Fanconi Renotubular Syndrome 2 40 0.028
767
ALC005 Alcoholic Pancreatitis 40 0.028
768
CRB086 Cerebral Aneurysms 40 0.028
769
OCL010 Ocular Hypotension 39 0.028
770
FLL031 Follicular Adenoma 39 0.028
771
HYP141 Hyperphenylalaninemia 39 0.028
772
CRV030 Cervical Adenitis 38 0.028
773
SRT003 Sertoli-Leydig Cell Tumor 38 0.028
774
MLN003 Melancholia 38 0.028
775
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.028
776
P CRB059 Cerebellar Degeneration 37 0.028
777
ATN021 Autoinflammatory Syndrome 36 0.028
778
PLM011 Plummer's Disease 35 0.028
779
GRM010 Germ Cells Tumors 34 0.028
780
FML168 Familial Isolated Pituitary Adenoma 33 0.028
781
ACN019 Acanthamoeba Keratitis 31 0.028
782
c SCH064 Schizophrenia 10 31 0.028
783
c PRG019 Paragangliomas 2 31 0.028
784
c HRD198 Hereditary Dystonia 30 0.028
785
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.028
787
HGH001 High Pressure Neurological Syndrome 28 0.028
788
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.028
790
CHL079 Children's Interstitial Lung Disease 26 0.028
791
ACT162 Acute Sensory Ataxic Neuropathy 26 0.028
792
ASB003 Asbestos Intoxication 26 0.028
793
TRC123 Trichohepatoneurodevelopmental Syndrome 25 0.028
794
ACR079 Acrodysostosis with Multiple Hormone Resistance 24 0.028
795
c ATS376 Autism 15 24 0.028
796
ANS017 Anosmia, Isolated Congenital 24 0.028
797
c RNG021 Ring Chromosome 5 23 0.028
798
MST022 Masticatory Muscles, Hypertrophy of 18 0.028
799
c PGM012 Pigmented Nodular Adrenocortical Disease, Primary, 3 17 0.028
800
MYP026 Myopathy - Thyrotoxic 17 0.028
801
NVL002 Novelty Seeking Personality Trait 16 0.028
802
MTR086 Motor Stereotypies 16 0.028
803
NCL008 Nuclear Ribonucleic Acid 16 0.028
804
FRC013 Fructose Utilization 15 0.028
805
c ANT081 Antigen Defined by Monoclonal Antibody T87 13 0.028
806
PRP074 Peripheral Resistance to Thyroid Hormones 11 0.028
807
EPT028 Epithelial Basolateral Chloride Conductance Regulator, Rabbit, Homolog of 10 0.028
Content
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