Search results for 12(R)-HPETE

1669 hits were found for 12(R)-HPETE

# Family MCID Name MIFTS Score
1
P BCL017 B-Cell Lymphoma 58 0.360
2
P LYM118 Lymphoma 68 0.338
3
DFF005 Diffuse Large B-Cell Lymphoma 56 0.331
4
LYM019 Lymphosarcoma 47 0.284
5
48X005 48,xyyy 39 0.231
6
P LYM031 Lymphocytic Leukemia 55 0.218
7
HMN044 Human Immunodeficiency Virus Type 1 71 0.213
8
DWN001 Down Syndrome 70 0.213
9
LYM133 Lymphoma, Hodgkin, Classic 69 0.206
10
RTC005 Reticulosarcoma 49 0.202
11
P LKM002 Leukemia 66 0.188
12
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.186
13
P PRS038 Personality Disorder 65 0.182
14
P HPT021 Hepatitis 67 0.180
15
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.178
16
CHR178 Chromosomal Triplication 35 0.176
17
P NTR004 Neutropenia 63 0.175
18
c HPT001 Hepatitis C 63 0.172
19
c RHB024 Rhabdomyosarcoma 2 65 0.164
20
MNT001 Mantle Cell Lymphoma 66 0.163
21
ACQ007 Acquired Immunodeficiency Syndrome 60 0.161
22
c PRM038 Primary Agammaglobulinemia 43 0.161
23
c HPT073 Hepatitis C Virus 70 0.159
24
P FLL037 Follicular Lymphoma 66 0.159
25
IMM167 Immune Deficiency Disease 78 0.158
26
HLX001 Helix Syndrome 47 0.156
27
c LKM071 Leukemia, Chronic Lymphocytic 79 0.156
28
c LKM061 Leukemia, Acute Myeloid 83 0.155
29
47X002 47,xyy 49 0.153
30
ADL002 Adult Syndrome 69 0.153
31
P LKM062 Leukemia, Acute Lymphoblastic 68 0.151
32
MYL009 Myelodysplastic Syndrome 70 0.150
33
DFC004 Deficiency Anemia 75 0.149
34
P MYL006 Myeloid Leukemia 60 0.149
35
AVD001 Avoidant Personality Disorder 54 0.147
36
ANX010 Anxiety 72 0.144
37
P BRS047 Breast Cancer 96 0.142
38
P NRP001 Neuropathy 56 0.142
39
P ATS364 Autism 65 0.141
40
P INF032 Infertility 57 0.140
41
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.137
42
P DRR001 Diarrhea 57 0.137
43
c HPT003 Hepatitis a 63 0.137
44
DPR016 Depression 63 0.137
45
MYL069 Myeloma, Multiple 85 0.135
46
P NRB001 Neuroblastoma 71 0.135
47
c HYP595 Hypertension, Essential 84 0.134
48
P KDN018 Kidney Disease 70 0.134
49
P TRN020 Turner Syndrome 65 0.134
50
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.134
51
P CLR023 Colorectal Cancer 98 0.133
52
ISC004 Ischemia 60 0.131
53
CYS001 Cystic Fibrosis 80 0.131
54
P ADN016 Adenocarcinoma 64 0.131
55
AST005 Asthma 77 0.131
56
P RNG032 Ring Chromosome 42 0.130
57
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.130
58
P DBT009 Diabetes Mellitus 64 0.129
59
ALC007 Alcohol Dependence 66 0.128
60
SVR004 Severe Combined Immunodeficiency 73 0.125
61
MNT002 Mental Depression 57 0.125
62
P THR014 Thrombocytopenia 68 0.123
63
ATM095 Autoimmune Disease 61 0.123
64
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.122
65
DRM006 Dermatitis 61 0.120
66
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.120
67
P CRN018 Coronary Artery Anomaly 63 0.120
68
LVR012 Liver Cirrhosis 63 0.120
69
VRL011 Viral Infectious Disease 61 0.117
70
ALL026 Allergic Hypersensitivity Disease 64 0.117
71
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.116
72
MSL001 Measles 61 0.116
73
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.116
74
P OVR042 Ovarian Cancer 89 0.115
75
P ALZ034 Alzheimer Disease 88 0.115
76
LNG099 Lung Disease 61 0.115
77
CNG034 Congestive Heart Failure 70 0.114
78
c PRC016 Pre-Eclampsia 63 0.114
79
OST012 Osteoarthritis 78 0.113
80
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.113
81
P BLD134 Bladder Cancer 78 0.113
82
P LNG032 Lung Cancer 97 0.112
83
P LVR013 Liver Disease 68 0.112
84
PRT037 Pertussis 65 0.112
85
c ATS007 Autism Spectrum Disorder 67 0.111
86
P CRN300 Coronary Heart Disease 1 63 0.111
87
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.111
88
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.110
89
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.109
90
c HYP836 Hypercholesterolemia, Familial, 1 72 0.109
91
CYT002 Cytokine Deficiency 44 0.108
92
ADN018 Adenoma 58 0.107
93
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.107
94
ART140 Arteries, Anomalies of 53 0.107
95
c ACT075 Acute Myocardial Infarction 56 0.106
96
IRN002 Iron Metabolism Disease 57 0.106
97
P HRT032 Heart Disease 75 0.104
98
c FLL041 Follicular Lymphoma 1 49 0.104
99
P SZR006 Seizure Disorder 58 0.104
100
CRB039 Cerebrovascular Disease 69 0.104
101
P PSR002 Psoriasis 62 0.104
102
P LTR001 Lateral Sclerosis 53 0.104
103
P PRP019 Peripheral Nervous System Disease 57 0.103
104
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.103
105
HRW001 Hair Whorl 36 0.103
106
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.103
107
P ATR011 Atrial Fibrillation 66 0.102
108
PST011 Pustulosis of Palm and Sole 52 0.102
109
P RHM011 Rheumatoid Arthritis 80 0.101
110
BRK010 Burkitt Lymphoma 67 0.101
111
P GLM045 Glioma 63 0.101
112
c ACT073 Acute Leukemia 58 0.101
113
TRM010 Traumatic Brain Injury 53 0.100
114
P MJR001 Major Depressive Disorder 68 0.100
115
HMP009 Haemophilus Influenzae 42 0.100
116
TTN003 Tetanus 64 0.099
117
STR067 Stroke, Ischemic 80 0.099
118
GLB015 Glioblastoma Multiforme 75 0.098
119
GLL048 Glial Tumor 45 0.098
120
ETN001 Eating Disorder 59 0.097
121
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.097
122
HYP056 Hypoglycemia 66 0.097
123
P RHN004 Rhinitis 57 0.097
124
P PRS040 Prostate Cancer 97 0.097
125
P SBS003 Substance Abuse 54 0.097
126
P ALC033 Alcohol Use Disorder 58 0.096
127
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.096
128
P ART022 Arthritis 70 0.095
129
BCK006 Back Pain 42 0.095
130
P MYC007 Myocardial Infarction 70 0.095
131
VSL002 Visual Epilepsy 58 0.095
132
P PNC035 Pancreatic Cancer 84 0.095
133
P MMP001 Mumps 57 0.095
134
P MNN013 Meningitis 65 0.095
135
CHC001 Chickenpox 60 0.095
136
ANG054 Angina Pectoris 66 0.094
137
P PHC003 Pheochromocytoma 71 0.094
138
ANR007 Anorexia Nervosa 63 0.094
139
MLN008 Melanoma 69 0.093
140
P CHR345 Chronic Pain 50 0.093
141
END030 End Stage Renal Failure 58 0.093
142
DNT012 Dental Caries 51 0.093
143
ADR040 Adrenal Gland Pheochromocytoma 46 0.093
144
PRS045 Prostatic Hypertrophy 52 0.093
145
P EPL164 Epilepsy 71 0.093
146
P RBL001 Rubella 58 0.093
147
P PRK057 Parkinson Disease, Late-Onset 76 0.092
148
BRN071 Brain Injury 49 0.092
149
P TRM003 Tremor 53 0.092
150
P ENC004 Encephalitis 61 0.092
151
MDD011 Mood Disorder 62 0.092
152
PLS009 Plasma Cell Neoplasm 51 0.091
153
P VSC007 Vascular Disease 63 0.091
154
CNS004 Constipation 57 0.091
155
P HPT023 Hepatocellular Carcinoma 100 0.091
156
OCL069 Ocular Motor Apraxia 51 0.091
157
c SYS001 Systemic Lupus Erythematosus 86 0.091
158
P HDC001 Headache 57 0.091
159
PSY004 Psychotic Disorder 67 0.090
160
P GST053 Gastric Cancer 83 0.090
161
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.090
162
ALL003 Allergic Rhinitis 67 0.090
163
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.089
164
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.089
165
ATX019 Ataxia with Vitamin E Deficiency 48 0.089
166
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.089
167
P EXN002 Exanthem 57 0.088
168
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.088
169
CRV035 Cervical Cancer 76 0.088
170
P HRP006 Herpes Simplex 65 0.088
171
SKN016 Skin Disease 63 0.088
172
SQM006 Squamous Cell Carcinoma 60 0.088
173
PLM001 Pulmonary Tuberculosis 70 0.088
174
P CTR002 Cataract 60 0.087
175
PRS021 Prostatic Adenoma 51 0.087
176
PRS129 Prostatic Hyperplasia, Benign 49 0.087
178
SPN186 Spinal Cord Injury 60 0.086
179
HYP066 Hyperglycemia 61 0.085
180
P RSP003 Respiratory Failure 74 0.085
181
P ALP008 Alopecia 56 0.085
182
THY029 Thyroid Carcinoma 59 0.085
183
c HPT016 Hepatitis B 59 0.084
184
IMP005 Impotence 52 0.084
185
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.084
186
BCT022 Bacterial Infectious Disease 56 0.084
187
PNG002 Pain Agnosia 51 0.083
188
c BRN108 Branchiootic Syndrome 1 61 0.083
189
P DMN002 Dementia 67 0.083
190
P MLT020 Multiple Sclerosis 72 0.083
191
c MGR028 Migraine with or Without Aura 1 69 0.083
192
P OST002 Osteoporosis 73 0.083
193
P DRM053 Dermatitis, Atopic 66 0.083
194
P ENC018 Encephalopathy 61 0.083
195
P SRC025 Sarcoidosis 1 70 0.082
196
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.082
197
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.082
198
P GLM007 Glomerulonephritis 57 0.082
199
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.082
200
P SCH015 Schizophrenia 75 0.082
201
P BPL003 Bipolar Disorder 56 0.082
202
c CHR684 Chronic Kidney Disease 66 0.082
203
P PNC025 Panic Disorder 53 0.082
204
P ECL001 Eclampsia 51 0.082
205
P SLP006 Sleep Apnea 69 0.082
206
c ATR087 Atrial Standstill 1 74 0.082
207
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.082
208
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.082
209
SRC014 Sarcoma 65 0.081
210
c SML038 Small Cell Cancer of the Lung 65 0.081
211
c ACT068 Acute Cystitis 63 0.081
212
c PNS012 Paine Syndrome 61 0.081
213
VCC001 Vaccinia 49 0.081
214
P HYP086 Hypothyroidism 68 0.081
215
P PRD008 Periodontitis 62 0.080
216
LRN003 Learning Disability 49 0.080
217
c MJR024 Major Affective Disorder 9 41 0.080
218
c MJR022 Major Affective Disorder 8 38 0.080
219
SPN035 Spindle Cell Sarcoma 51 0.080
220
SPL018 Splenomegaly 48 0.080
221
AGN016 Aging 56 0.080
222
CHL079 Children's Interstitial Lung Disease 27 0.080
223
CRH001 Crohn's Disease 74 0.079
224
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.079
225
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.079
226
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.079
227
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.079
228
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.079
229
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.079
230
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.079
231
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.079
232
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.079
233
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.079
234
c FML035 Familial Hyperlipidemia 55 0.079
235
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.079
236
GRW007 Growth Hormone Deficiency 43 0.078
237
LPD008 Lipid Metabolism Disorder 62 0.078
238
GNR004 Generalized Anxiety Disorder 56 0.078
239
P HYP098 Hypereosinophilic Syndrome 66 0.078
240
DPH001 Diphtheria 60 0.077
241
c SPN225 Spondyloarthropathy 1 73 0.077
242
PLM031 Poliomyelitis 57 0.077
243
ATH013 Atherosclerosis Susceptibility 66 0.077
244
MRG003 Marginal Zone B-Cell Lymphoma 53 0.077
245
ULC004 Ulcerative Colitis 73 0.076
246
TYP007 Typhoid Fever 63 0.076
247
P RCT021 Rectum Cancer 53 0.076
248
P FBR017 Fibrosarcoma 56 0.075
249
BRN024 Bronchitis 68 0.075
250
P CRD119 Cardiac Arrest 67 0.075
251
GST092 Gastroesophageal Reflux 65 0.075
252
CHL014 Cholera 55 0.075
253
P SLM003 Salmonellosis 54 0.075
254
P LPR021 Leprosy 3 67 0.075
255
HNS001 Hansen's Disease 34 0.075
256
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.075
257
P MCR115 Microvascular Complications of Diabetes 5 66 0.075
258
P NRF023 Neurofibromatosis, Type Ii 76 0.075
259
SCL003 Social Phobia 48 0.074
260
CRB037 Cerebral Palsy 68 0.074
261
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.074
262
P END044 Endometriosis 62 0.074
263
P HML002 Hemolytic Anemia 62 0.074
264
c THR092 Thrombophilia Due to Thrombin Defect 73 0.074
265
P INS002 in Situ Carcinoma 52 0.074
266
P LPS004 Lupus Erythematosus 61 0.073
267
ATN004 Autonomic Neuropathy 44 0.073
268
P KDN017 Kidney Cancer 61 0.073
269
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.073
270
LWC001 Low Compliance Bladder 42 0.073
271
P LYM033 Lymphoproliferative Syndrome 60 0.073
272
LYM040 Lymphoblastic Lymphoma 54 0.073
273
CRD132 Cardiac Conduction Defect 59 0.073
274
P SCL018 Scoliosis 60 0.073
275
HRT011 Heart Septal Defect 50 0.073
276
ATN005 Autonomic Dysfunction 47 0.073
277
PLM033 Pulmonary Embolism 59 0.073
278
P CNT005 Central Nervous System Lymphoma 53 0.072
279
THR024 Thrombosis 56 0.072
280
P CRD246 Cardiovascular System Disease 56 0.072
281
c FNC043 Fanconi Anemia, Complementation Group E 62 0.072
282
APH002 Aphasia 57 0.071
283
OBS002 Obsessive-Compulsive Disorder 68 0.071
284
GST045 Gastroenteritis 59 0.071
285
P MCR010 Microcephaly 58 0.071
286
DYS015 Dysentery 50 0.071
287
CRB004 Cerebral Artery Occlusion 44 0.071
288
P INF037 Inflammatory Bowel Disease 56 0.070
289
PRN011 Pernicious Anemia 52 0.070
290
P INF038 Influenza 68 0.070
291
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.070
292
P SYP003 Syphilis 59 0.070
293
DYS009 Dysthymic Disorder 48 0.070
294
P BNG032 Benign Mesothelioma 45 0.070
295
P SLP005 Sleep Disorder 59 0.069
296
STM007 Stomatitis 49 0.069
297
P AST007 Astrocytoma 50 0.069
298
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.069
299
P PLY019 Polyneuropathy 56 0.069
300
INS024 Insulin-Like Growth Factor I 79 0.069
301
HYP266 Hypoxia 56 0.069
302
NTR005 Nutritional Deficiency Disease 61 0.069
303
P GRV001 Graves' Disease 55 0.069
304
RRS014 Rare Surgical Neurologic Disease 32 0.069
305
SKN019 Skin Melanoma 67 0.069
306
P MYP006 Myopia 55 0.069
307
HPR003 Heparin-Induced Thrombocytopenia 47 0.068
308
P CHR285 Chronic Myelomonocytic Leukemia 59 0.068
309
MLR004 Malaria 80 0.068
310
BNR002 Bone Resorption Disease 48 0.068
311
HDN002 Head Injury 45 0.068
312
P GRF003 Graft-Versus-Host Disease 71 0.068
313
RHM027 Rheumatic Disease 56 0.068
314
ANR040 Aneurysm 58 0.068
315
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.067
316
ATR057 Atrioventricular Block 55 0.067
317
DSS008 Disease of Mental Health 57 0.067
318
PNC001 Pancytopenia 54 0.067
319
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.067
320
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.067
321
CMR002 Coumarin Resistance 56 0.067
322
c PRM226 Primary Central Nervous System Lymphoma 47 0.067
323
P GLM040 Glioma Susceptibility 1 81 0.067
324
SYN036 Syncope 45 0.067
325
BRD004 Borderline Personality Disorder 53 0.066
326
P APL001 Aplastic Anemia 74 0.066
327
HMT002 Hematologic Cancer 62 0.066
328
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.066
330
P ANR048 Aniridia 1 63 0.066
331
P TRC086 Trichohepatoenteric Syndrome 1 59 0.066
332
P SKN015 Skin Carcinoma 67 0.066
333
P PLY018 Polycythemia 55 0.065
334
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.065
335
P MSC003 Muscular Atrophy 52 0.065
336
END057 Endometrial Cancer 74 0.065
337
INT007 Intermediate Coronary Syndrome 55 0.065
338
PRT036 Peritonitis 65 0.065
339
BLM002 Bulimia Nervosa 57 0.065
340
c ACT071 Acute Kidney Failure 59 0.064
341
ING001 Inguinal Hernia 60 0.064
342
P RTN024 Retinoblastoma 72 0.064
343
c FML008 Familial Retinoblastoma 53 0.064
344
SFT003 Soft Tissue Sarcoma 56 0.064
345
P DDN001 Duodenal Ulcer 50 0.064
346
P DYS154 Dystonia 65 0.064
347
P FRN006 Frontotemporal Dementia 70 0.064
348
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.064
349
SCH014 Schistosomiasis 56 0.063
350
P HMP007 Hemophilia 51 0.063
351
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.063
352
PPL022 Papilloma 54 0.063
353
P TRT010 Teratoma 51 0.063
354
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.063
355
P GND004 Gonadal Dysgenesis 49 0.063
356
c HYP272 Hypercholesterolemia, Familial, 3 43 0.063
357
NRL016 Neural Tube Defects 82 0.063
358
P END033 Endocarditis 57 0.063
359
PLY001 Polycythemia Vera 69 0.063
360
c PSR017 Psoriasis 2 52 0.063
361
c PSR023 Psoriasis 1 49 0.063
362
c PSR028 Psoriasis 7 39 0.063
363
c PSR032 Psoriasis 11 38 0.063
364
c PSR018 Psoriasis 13 38 0.063
365
P MSC005 Muscular Dystrophy 66 0.063
366
MTH009 Mouth Disease 56 0.063
367
P ART018 Aortic Valve Insufficiency 53 0.063
368
PST028 Post-Traumatic Stress Disorder 58 0.063
369
OTT002 Otitis Media 71 0.062
370
LSH001 Leishmaniasis 63 0.062
371
FTT001 Fatty Liver Disease 61 0.062
372
BRN002 Bronchiolitis 59 0.062
373
P KLZ004 Kala-Azar 1 41 0.062
374
LMY002 Leiomyoma 50 0.062
375
OVR029 Ovarian Hyperstimulation Syndrome 63 0.062
376
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.062
377
P ATX030 Ataxia-Telangiectasia 83 0.062
378
HYP005 Hypokalemia 55 0.062
379
PST021 Postpartum Depression 50 0.062
380
CND002 Conduct Disorder 51 0.062
381
MCR004 Macroglobulinemia 50 0.062
382
HYP080 Hypogonadism 50 0.062
383
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.062
384
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.062
385
CHR074 Choriocarcinoma 46 0.062
386
THR013 Thoracic Outlet Syndrome 53 0.062
387
VSC002 Vascular Dementia 57 0.062
388
SPS057 Spasticity 41 0.061
389
SPN051 Spondylitis 52 0.061
390
INF009 Inflammatory Spondylopathy 32 0.061
391
ACT084 Acute Stress Disorder 48 0.061
392
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.061
393
CLT003 Colitis 62 0.061
394
P STR020 Strabismus 56 0.061
395
EWN003 Ewing Sarcoma 68 0.060
396
ART002 Arts Syndrome 63 0.060
397
RGH001 Right Bundle Branch Block 47 0.060
398
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.060
399
P MYC084 Mycobacterium Tuberculosis 1 68 0.060
400
SBC016 Subacute Delirium 44 0.060
401
SQM002 Squamous Cell Papilloma 42 0.060
402
P VSC011 Vasculitis 62 0.060
403
c DLT002 Dilated Cardiomyopathy 79 0.060
404
HMS001 Hemosiderosis 54 0.060
405
HYP064 Hypogonadotropism 40 0.060
406
IGR001 Ige Responsiveness, Atopic 59 0.060
407
P HYD006 Hydrocephalus 65 0.060
408
RCK004 Rickets 69 0.059
409
ACR007 Acromegaly 71 0.059
410
PRP030 Purpura 55 0.059
411
MCH006 Mechanical Strabismus 39 0.059
412
PPT005 Peptic Ulcer Disease 58 0.059
413
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.059
414
c CHR064 Chronic Monocytic Leukemia 34 0.059
415
P RRH023 Rare Hereditary Hemochromatosis 41 0.059
416
VTM002 Vitamin B12 Deficiency 48 0.059
417
LYM012 Lymphoplasmacytic Lymphoma 61 0.059
418
TXC005 Toxic Shock Syndrome 61 0.058
419
TLN003 Telangiectasis 51 0.058
420
c MCR120 Microvascular Complications of Diabetes 7 47 0.058
421
P BRS044 Breast Adenocarcinoma 59 0.058
422
P HYP076 Hyperthyroidism 55 0.058
423
OST017 Osteomyelitis 64 0.058
424
P PLY011 Polycystic Ovary Syndrome 56 0.058
425
SCH012 Schizoaffective Disorder 50 0.058
426
PPL052 Papillomatosis, Confluent and Reticulated 34 0.058
427
P CNR004 Cone-Rod Dystrophy 2 71 0.058
428
IRR002 Irritable Bowel Syndrome 63 0.058
429
PRP016 Paraplegia 53 0.058
430
HRP004 Herpes Zoster 60 0.057
431
SCH003 Schizophreniform Disorder 56 0.057
432
LNG031 Lung Benign Neoplasm 50 0.057
433
ESP021 Esophageal Cancer 90 0.057
434
LYM027 Lymphopenia 57 0.057
435
ENT004 Enthesopathy 48 0.057
436
KPS004 Kaposi Sarcoma 75 0.057
437
MCS002 Mucositis 55 0.057
438
PST092 Posttransplant Acute Limbic Encephalitis 29 0.057
439
P ANG001 Angelman Syndrome 67 0.057
440
PNC129 Pancreatic Adenocarcinoma 67 0.057
441
EPD015 Epidemic Typhus 46 0.057
442
P LNG064 Lung Cancer Susceptibility 3 77 0.057
443
P THL005 Thalassemia 60 0.057
444
P MLN007 Male Infertility 56 0.057
445
ALL006 Allergic Asthma 56 0.057
446
P MTR003 Mitral Valve Stenosis 50 0.057
447
P LMY004 Leiomyosarcoma 62 0.057
448
LPT014 Leptin Deficiency or Dysfunction 73 0.056
449
IDP011 Idiopathic Interstitial Pneumonia 63 0.056
450
P PLM036 Pulmonary Fibrosis 61 0.056
451
SYN007 Synovitis 55 0.056
452
NRT001 Neurotic Disorder 52 0.056
453
CRD137 Cardiogenic Shock 48 0.056
454
P PNM007 Pneumonia 68 0.056
455
P PLM037 Pulmonary Hypertension 68 0.056
456
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.056
457
P PRV006 Pervasive Developmental Disorder 57 0.056
458
P ART023 Arthropathy 62 0.056
459
c MTR002 Mitral Valve Insufficiency 47 0.056
460
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.056
461
FCT007 Factor Vii Deficiency 66 0.056
462
ALL014 Allergic Encephalomyelitis 39 0.056
463
HDG004 Hodgkin's Granuloma 26 0.056
464
HDG006 Hodgkin's Paragranuloma 24 0.056
465
c LPM012 Lipomatosis, Multiple 59 0.056
466
PLM005 Pleomorphic Lipoma 39 0.056
467
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.056
468
P RHB003 Rhabdomyosarcoma 62 0.056
469
c ACT027 Acute Pancreatitis 59 0.056
470
HYD002 Hydronephrosis 59 0.056
471
P HNT016 Huntington Disease 71 0.055
472
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.055
473
INT002 Intermittent Claudication 61 0.055
475
P MVM001 Movement Disease 61 0.055
476
EYD002 Eye Disease 58 0.055
477
P SNS001 Sensorineural Hearing Loss 61 0.055
478
P FRG001 Fragile X Syndrome 68 0.055
479
P UVT001 Uveitis 57 0.055
480
P HYP750 Hypertriglyceridemia, Familial 61 0.055
481
P PLY014 Polycystic Kidney Disease 59 0.055
482
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.055
483
END040 Endogenous Depression 54 0.055
484
PRP036 Peripheral T-Cell Lymphoma 53 0.054
485
c PCH010 Pachyonychia Congenita 3 43 0.054
486
TBC004 Tobacco Addiction 64 0.054
487
P SPN046 Spinal Muscular Atrophy 64 0.054
488
CYT008 Cytomegalovirus Infection 56 0.054
489
DWR001 Dwarfism 44 0.054
490
WLF001 Wolff-Parkinson-White Syndrome 65 0.054
491
OPP004 Oppositional Defiant Disorder 49 0.054
492
P MTR014 Motor Neuron Disease 64 0.054
493
GRN017 Granulocytopenia 44 0.054
494
FDL002 Food Allergy 49 0.054
495
c ART101 Aortic Valve Disease 2 63 0.054
496
AMN001 Amenorrhea 54 0.054
497
DYS073 Dysphagia 50 0.054
498
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.054
499
c FML021 Familial Hypercholesterolemia 68 0.054
500
c ACT135 Acute Graft Versus Host Disease 51 0.053
501
P ATR010 Atrial Heart Septal Defect 60 0.053
502
INS001 Insulinoma 60 0.053
503
STT001 Status Epilepticus 59 0.053
504
P THY032 Thyroiditis 53 0.053
505
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.053
506
CHG001 Chagas Disease 66 0.053
507
LFT001 Left Bundle Branch Hemiblock 49 0.053
508
P CYS018 Cystitis 59 0.053
509
DSS009 Disseminated Intravascular Coagulation 57 0.053
510
PRC013 Pericarditis 54 0.053
511
c MCR113 Microvascular Complications of Diabetes 3 52 0.053
512
c MCR130 Microvascular Complications of Diabetes 6 41 0.053
513
c MCR133 Microvascular Complications of Diabetes 4 41 0.053
514
AMN003 Amnestic Disorder 54 0.052
515
P TMP001 Temporal Lobe Epilepsy 50 0.052
516
CRN030 Coronary Stenosis 50 0.052
517
ART016 Aortic Aneurysm 68 0.052
518
P AMY004 Amyloidosis 70 0.052
519
CRD223 Cardiac Arrhythmia 60 0.052
520
P TCL004 T-Cell Leukemia 47 0.052
521
49X006 49, Xxxxy Syndrome 41 0.052
522
P BND020 Bone Disease 59 0.052
523
P MYP004 Myopathy 64 0.052
524
ATS010 Autosomal Recessive Disease 48 0.052
525
PRP027 Peripheral Vascular Disease 71 0.052
526
OST003 Osteonecrosis 61 0.052
527
P CLC063 Celiac Disease 1 68 0.052
528
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.052
529
MYL005 Myelofibrosis 67 0.052
530
c FML001 Familial Atrial Fibrillation 66 0.051
531
NNL006 Non-Alcoholic Steatohepatitis 51 0.051
532
AZS001 Azoospermia 50 0.051
533
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.051
534
P SCK002 Sick Sinus Syndrome 55 0.051
535
P OVR082 Overgrowth Syndrome 50 0.051
536
P RRT020 Rare Tumor 41 0.051
537
P GST044 Gastritis 55 0.051
538
P MGL001 Megaloblastic Anemia 55 0.051
539
SPP010 Suppressor of Tumorigenicity 3 51 0.051
540
THY122 Thyroid Gland Cancer 58 0.051
541
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.051
542
HRY003 Hairy Cell Leukemia 55 0.050
543
P HYP730 Hypogonadotropic Hypogonadism 53 0.050
544
AND002 Androgen Insensitivity Syndrome 66 0.050
545
KHL003 Kohlschutter-Tonz Syndrome 64 0.050
546
c SCL052 Scleroderma, Familial Progressive 62 0.050
547
P PTT006 Pituitary Adenoma 54 0.050
548
P ESP024 Esophagitis 62 0.050
549
P HYP265 Hypotonia 42 0.050
550
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.050
551
P NPH012 Nephrotic Syndrome 63 0.050
552
MNN042 Meningioma, Radiation-Induced 62 0.050
553
P SCK005 Sickle Cell Disease 50 0.049
554
SXL003 Sexual Disorder 48 0.049
555
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.049
556
MYL031 Myeloproliferative Neoplasm 65 0.049
557
ADP007 Adie Pupil 39 0.049
558
HPT082 Hepatic Adenomas, Familial 37 0.049
559
P HYP061 Hypertrophic Cardiomyopathy 66 0.049
560
c MLG068 Malignant Glioma 45 0.049
561
IDP070 Idiopathic Scoliosis 37 0.049
562
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.049
563
P VNT002 Ventricular Septal Defect 60 0.049
564
AST006 Astigmatism 47 0.049
565
GST019 Gastrointestinal Stromal Tumor 76 0.049
566
c BSL007 Basal Cell Carcinoma 68 0.049
567
CHL065 Cholangiocarcinoma 67 0.049
568
P CNJ013 Conjunctivitis 65 0.049
569
CLN015 Colon Adenocarcinoma 63 0.049
570
P SJG008 Sjogren Syndrome 56 0.049
571
HYP060 Hyperinsulinism 54 0.049
572
INT079 Intrahepatic Cholangiocarcinoma 50 0.049
573
c FNC027 Fanconi Anemia, Complementation Group a 81 0.049
574
LYM017 Lyme Disease 63 0.049
575
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.049
576
KRT006 Keratoconjunctivitis 53 0.049
577
HNM002 Hinman Syndrome 29 0.049
578
PLG002 Plague 57 0.049
579
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.049
580
c DWL002 Dowling-Degos Disease 1 58 0.048
581
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.048
582
ERY051 Erythroleukemia, Familial 56 0.048
583
GST023 Gastric Ulcer 53 0.048
584
DGN001 Degenerative Disc Disease 48 0.048
585
DBT002 Diabetic Autonomic Neuropathy 41 0.048
586
JPN002 Japanese Encephalitis 54 0.048
587
KRT009 Keratosis 53 0.048
588
WHP002 Whiplash 36 0.048
589
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.048
590
GNG013 Gingivitis 59 0.047
591
GLS001 Gliosarcoma 54 0.047
592
c SVR001 Severe Acute Respiratory Syndrome 55 0.047
593
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.047
594
P CRN025 Corneal Dystrophy 45 0.047
595
CNT047 Contact Dermatitis 57 0.047
596
P FBR031 Febrile Seizures 51 0.047
597
P HYP040 Hypospadias 51 0.047
598
c MNN043 Meningioma, Familial 74 0.047
599
P PTS002 Ptosis 52 0.047
600
P NSP012 Nasopharyngeal Carcinoma 67 0.047
601
MLT157 Multiple System Atrophy 1 70 0.047
602
P THR117 Three M Syndrome 1 63 0.047
603
P PTN014 Patent Ductus Arteriosus 1 60 0.047
604
PRP080 Peripheral Artery Disease 53 0.047
605
HYP081 Hypolipoproteinemia 50 0.047
606
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.047
607
P ASP006 Aspergillosis 66 0.046
608
P HYP069 Hyperparathyroidism 62 0.046
609
c DRM054 Dermatitis, Atopic, 2 45 0.046
610
PRT013 Portal Hypertension 60 0.046
611
HYP748 Hypertelorism 50 0.046
612
SPN021 Spinal Meningioma 47 0.046
613
TRN018 Transitional Cell Carcinoma 56 0.046
614
OST159 Osteogenic Sarcoma 66 0.046
615
PLM010 Pulmonary Edema 55 0.046
616
GLC003 Glucose Intolerance 54 0.046
617
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.046
618
c MLG074 Malignant Mesenchymoma 39 0.046
619
P ART005 Arteriovenous Malformation 65 0.046
620
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.046
621
PNM008 Pneumothorax 56 0.046
622
GTR002 Goiter 52 0.046
623
SCR001 Secretory Meningioma 37 0.046
624
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.046
625
P THY023 Thymoma 65 0.046
626
c THY107 Thymoma, Familial 54 0.046
627
MTB004 Metabolic Acidosis 50 0.046
628
PLL012 Pollen Allergy 45 0.046
629
PRS063 Paresthesia 43 0.046
630
c CHR682 Chronic Bilirubin Encephalopathy 38 0.046
631
RHM001 Rheumatic Fever 61 0.046
632
P TXP001 Toxoplasmosis 60 0.046
633
FBR047 Fibromyalgia 59 0.046
634
P PLV020 Pelvic Organ Prolapse 59 0.046
635
HMP005 Hemiplegia 54 0.046
636
P ART021 Arteriosclerosis 54 0.046
637
P RTN016 Retinal Degeneration 53 0.046
638
HMC014 Homocysteinemia 53 0.046
639
PST046 Post-Transplant Lymphoproliferative Disease 53 0.046
640
SBS004 Substance Dependence 48 0.045
641
DRG003 Drug Dependence 47 0.045
642
P INT070 Intestinal Obstruction 58 0.045
643
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.045
644
c MST023 Mesothelioma, Malignant 57 0.045
645
SPN019 Spondylolisthesis 49 0.045
646
IGG001 Iga Glomerulonephritis 48 0.045
647
P PNC044 Pancreatitis 61 0.045
648
GST033 Gestational Diabetes 57 0.045
649
P OPN001 Open-Angle Glaucoma 49 0.045
650
CLF027 Cleft Palate, Isolated 64 0.045
651
FCL014 Focal Epilepsy 54 0.045
652
P KRT007 Keratoconus 49 0.045
653
RST023 Resting Heart Rate, Variation in 41 0.045
654
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.045
655
c HMP029 Hemophilia a 65 0.045
656
FCT001 Factor Viii Deficiency 55 0.045
657
RCH001 Richter's Syndrome 45 0.045
658
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.045
659
ORL011 Oral Cancer 60 0.045
660
P MYC008 Myocarditis 59 0.045
661
THY124 Thyroid Gland Papillary Carcinoma 52 0.045
662
PLC008 Placenta Disease 49 0.045
663
TRN015 Transient Cerebral Ischemia 62 0.044
664
ECT026 Ectopic Pregnancy 49 0.044
665
P OPT006 Optic Nerve Disease 57 0.044
666
DBT010 Diabetic Neuropathy 55 0.044
667
P VNW001 Von Willebrand's Disease 64 0.044
668
OPT003 Opiate Dependence 50 0.044
669
INF013 Inferior Myocardial Infarction 33 0.044
670
FBR012 Fabry Disease 71 0.044
671
CTN007 Cutaneous Leishmaniasis 61 0.044
672
P INT143 Interstitial Cystitis 61 0.044
673
CMP010 Complex Regional Pain Syndrome 58 0.044
674
P CND004 Candidiasis 57 0.044
675
PRS047 Prostatitis 56 0.044
676
BRN014 Bronchopneumonia 50 0.044
677
c PRS136 Prostate Cancer, Hereditary, 6 33 0.044
678
c PRS130 Prostate Cancer, Hereditary, 8 32 0.044
679
ARG004 Argyria 28 0.044
680
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.043
681
P CHL066 Cholangitis 50 0.043
682
OVR094 Ovarian Epithelial Cancer 38 0.043
683
P MYS003 Myasthenia Gravis 68 0.043
684
ILS001 Ileus 51 0.043
685
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.043
686
P MYT002 Myotonic Dystrophy 49 0.043
687
ANX004 Anoxia 42 0.043
688
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.043
689
PLS025 Plasmablastic Lymphoma 47 0.043
690
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.043
691
APP008 Appendicitis 60 0.043
692
KRT001 Keratoconjunctivitis Sicca 50 0.043
693
c MCR129 Microvascular Complications of Diabetes 1 66 0.043
694
c DYS056 Dystonia 12 64 0.043
695
MCL006 Macular Retinal Edema 55 0.043
696
RFR010 Refractory Anemia 48 0.043
697
MST005 Mastitis 53 0.043
698
DRM011 Dermatophytosis 52 0.043
699
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 59 0.042
700
P PYL005 Pyelonephritis 56 0.042
701
RTC009 Reticulum Cell Sarcoma 43 0.042
702
SDD001 Sudden Infant Death Syndrome 61 0.042
703
TXC002 Toxic Encephalopathy 52 0.042
704
ISL003 Isolated Growth Hormone Deficiency 52 0.042
705
P NRC002 Narcolepsy 51 0.042
706
VRC005 Varicose Veins 60 0.042
707
P BRN022 Bronchiectasis 59 0.042
708
NRN004 Neuroendocrine Tumor 55 0.042
709
NRT004 Neuritis 53 0.042
710
CHL122 Cholesteatoma of Middle Ear 51 0.042
711
CLR109 Colorectal Adenocarcinoma 50 0.042
712
DRY001 Dry Eye Syndrome 47 0.042
713
P MYC033 Myoclonus 46 0.042
714
PTT037 Pituitary Tumors 44 0.042
715
GT001 Gout 63 0.042
716
GLS018 Glass Syndrome 53 0.042
717
RFR003 Refractive Error 44 0.042
718
CHK001 Chikungunya 53 0.042
719
DBT004 Diabetic Polyneuropathy 50 0.042
720
IMM136 Immune System Disease 45 0.042
721
PSR001 Psoriatic Arthritis 62 0.041
722
P HMN010 Hemangioma 61 0.041
723
c VRL010 Viral Hepatitis 51 0.041
724
APN008 Apnea, Obstructive Sleep 65 0.041
725
c VSC019 Vesicoureteral Reflux 1 59 0.041
726
BRS051 Breast Disease 58 0.041
727
BRN004 Brain Edema 55 0.041
728
SNS003 Sensory Peripheral Neuropathy 53 0.041
729
ONC002 Onchocerciasis 51 0.041
730
SMT001 Somatization Disorder 48 0.041
731
ANV001 Anovulation 47 0.041
732
c PRM163 Primary Mediastinal Large B-Cell Lymphoma 41 0.041
733
SCH011 Schizotypal Personality Disorder 39 0.041
734
SCK003 Sickle Cell Anemia 72 0.041
735
CHR066 Chronic Fatigue Syndrome 61 0.041
736
DCB001 Decubitus Ulcer 60 0.041
737
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.041
738
APR001 Apraxia 51 0.041
739
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.041
740
URM002 Uremia 49 0.041
741
c WLM018 Wilms Tumor 5 62 0.041
742
P PRM006 Primary Biliary Cirrhosis 61 0.041
743
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.041
744
OCL006 Ocular Hypertension 53 0.041
745
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.041
746
P SYS005 Systemic Scleroderma 70 0.040
747
ACT119 Acute Promyelocytic Leukemia 63 0.040
748
INT075 Intracranial Hypertension 53 0.040
749
KHN001 Kuhnt-Junius Degeneration 48 0.040
750
PFF001 Pfeiffer Syndrome 79 0.040
751
RDC002 Radiculopathy 48 0.040
752
PPL002 Papillary Carcinoma 47 0.040
753
P SCL057 Scoliosis, Isolated 1 41 0.040
754
MSC157 Muscular Dystrophy, Duchenne Type 71 0.040
755
ANG020 Angiosarcoma 58 0.040
756
VSC003 Visceral Leishmaniasis 55 0.040
757
CMM004 Common Variable Immunodeficiency 67 0.040
758
c GRV008 Graves Disease 1 55 0.040
759
P LYM025 Lymphedema 53 0.040
760
PLS007 Plasmodium Falciparum Malaria 52 0.040
761
PTH003 Pathologic Nystagmus 51 0.040
762
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.040
763
BRN056 Bronchopulmonary Dysplasia 57 0.040
764
MSN004 Mesenchymal Cell Neoplasm 41 0.040
765
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.040
766
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.040
767
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.039
768
ART001 Arterial Tortuosity Syndrome 66 0.039
769
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.039
770
PLS011 Plasmacytoma 56 0.039
771
CLF001 Cleft Lip 53 0.039
772
AMB002 Amblyopia 50 0.039
773
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.039
774
SPP007 Suppression Amblyopia 39 0.039
775
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.039
776
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.039
777
OPD006 Opioid Addiction 48 0.039
778
PLY100 Polyploidy 40 0.039
779
DSS010 Dissociative Disorder 38 0.039
781
c PST001 Posterior Myocardial Infarction 22 0.039
782
CLR108 Colorectal Adenoma 64 0.039
783
CHL068 Cholestasis 60 0.039
784
HLC007 Helicobacter Pylori Infection 59 0.039
785
INT051 Intussusception 53 0.039
786
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.039
787
BRC012 Brucellosis 61 0.039
788
P ALP009 Alopecia Areata 60 0.039
789
SPN027 Spinal Stenosis 59 0.039
790
P PLY006 Polydactyly 58 0.039
791
P INT068 Intestinal Disease 52 0.039
792
P SML001 Small Cell Carcinoma 52 0.039
793
PPL001 Papillary Adenoma 45 0.039
794
HRP008 Herpes Simiae 25 0.039
795
PHN003 Phenylketonuria 75 0.039
796
BRR014 Barrett Esophagus 64 0.039
797
P URT039 Urticaria 58 0.039
798
SPP011 Suppression of Tumorigenicity 12 59 0.038
799
PRT058 Pure Autonomic Failure 59 0.038
800
CCC001 Coccidioidomycosis 53 0.038
801
HND015 Hand Skill, Relative 33 0.038
802
P TBR001 Tuberous Sclerosis 70 0.038
803
P ANP001 Anaplastic Large Cell Lymphoma 61 0.038
804
MMM001 Mammary Paget's Disease 53 0.038
805
c LTN004 Late-Onset Retinal Degeneration 52 0.038
806
LPT006 Leptin Receptor Deficiency 47 0.038
807
MXD026 Mixed Glioma 45 0.038
808
P ALP106 Alport Syndrome 1, X-Linked 55 0.038
809
MYC006 Mycosis Fungoides 66 0.038
810
P SHR029 Short Syndrome 57 0.038
811
EXP004 Exophthalmos 52 0.038
812
GST040 Gastric Adenocarcinoma 70 0.038
813
SRC027 Sarcoma, Synovial 56 0.038
814
P BRG001 Brugada Syndrome 70 0.037
815
AVN001 Avian Influenza 56 0.037
816
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.037
817
P MMB011 Membranous Nephropathy 50 0.037
818
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 42 0.037
819
GST020 Gastric Antral Vascular Ectasia 41 0.037
820
SCR015 Scarlet Fever 40 0.037
821
P PRD006 Prader-Willi Syndrome 59 0.037
822
NWB001 Newborn Respiratory Distress Syndrome 58 0.037
823
CYS005 Cysticercosis 54 0.037
824
P THR015 Thrombophilia 50 0.037
825
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.037
826
c PLY105 Polycystic Ovary Syndrome 1 38 0.037
827
RRD056 Rare Disease in Surgical Orthopedic 28 0.037
828
FSC004 Fasciitis 50 0.037
829
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.037
830
BNG077 Benign Idiopathic Neonatal Seizures 26 0.037
831
P LNG028 Long Qt Syndrome 65 0.037
832
P ORT004 Orthostatic Intolerance 63 0.037
833
NRG002 Neurogenic Bladder 54 0.037
834
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.037
835
PTH002 Pathological Gambling 48 0.037
836
P PRR002 Pure Red-Cell Aplasia 48 0.037
837
RDC006 Red Cell Aplasia 42 0.037
838
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.037
839
P CHR071 Charcot-Marie-Tooth Disease 64 0.037
840
SMN007 Seminoma 44 0.037
841
P MJR007 Major Affective Disorder 1 43 0.037
842
NRL005 Neurilemmoma 60 0.036
843
IRN001 Iron Deficiency Anemia 58 0.036
844
ENT011 Enterocolitis 50 0.036
845
MYC088 Mycobacterium Avium Complex Infections 29 0.036
846
c SCN007 Secondary Hyperparathyroidism 50 0.036
847
CRV043 Cervical Dystonia 45 0.036
848
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.036
849
CRV045 Cervical Intraepithelial Neoplasia 39 0.036
850
c PSR033 Psoriasis 12 21 0.036
851
P FRD001 Friedreich Ataxia 63 0.036
852
BLR008 Bilirubin Metabolic Disorder 57 0.036
853
ALL010 Allergic Contact Dermatitis 55 0.036
854
CHR100 Chronic Ulcer of Skin 53 0.036
855
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.036
856
P END047 Endophthalmitis 52 0.036
857
DMY004 Demyelinating Disease 52 0.036
858
URT010 Ureteral Obstruction 46 0.036
859
c INF071 Inflammatory Bowel Disease 1 68 0.036
860
CHL123 Chlamydia 59 0.036
861
RSC001 Rosacea 55 0.036
862
CLF004 Cleft Lip/palate 54 0.036
863
NRM005 Neuromuscular Disease 63 0.035
864
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.035
865
LMB062 Limb Ischemia 55 0.035
866
VRC001 Varicocele 49 0.035
867
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.035
868
TTH006 Tooth Disease 46 0.035
869
P FML011 Familial Adenomatous Polyposis 72 0.035
870
KRN002 Kearns-Sayre Syndrome 63 0.035
871
PPL049 Papillon-Lefevre Syndrome 63 0.035
872
c GLC092 Glaucoma, Primary Open Angle 62 0.035
873
FLR002 Filariasis 55 0.035
874
P PMP001 Pemphigus 55 0.035
875
RHM028 Rheumatic Heart Disease 53 0.035
876
THR004 Thrombocytosis 51 0.035
877
ACH005 Achalasia 50 0.035
878
ACR006 Aceruloplasminemia 73 0.035
879
c JVN010 Juvenile Rheumatoid Arthritis 67 0.035
880
c HMP004 Hemophilia B 67 0.035
881
c THR082 Thrombophilia Due to Activated Protein C Resistance 60 0.035
882
DXT001 Dextrocardia 55 0.035
883
GNT002 Giant Cell Glioblastoma 52 0.035
884
TRC003 Trichomoniasis 52 0.035
885
c BPL002 Bipolar I Disorder 49 0.035
886
RTN020 Retinal Vascular Disease 48 0.035
887
P HMN032 Human Herpesvirus 8 46 0.035
888
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.035
889
ANT024 Anthrax Disease 58 0.035
890
SPC005 Speech Disorder 42 0.035
891
KLB003 Klebsiella Pneumonia 39 0.035
892
THY111 Thyroid Carcinoma, Familial Medullary 67 0.034
893
P ADL010 Adult Respiratory Distress Syndrome 63 0.034
894
CRY005 Cryptococcosis 58 0.034
895
SLC006 Silicosis 56 0.034
896
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.034
897
THY030 Thyroid Gland Disease 51 0.034
898
c HNT004 Huntington Disease-Like 2 49 0.034
899
VGN019 Vaginal Discharge 44 0.034
900
ORL015 Oral Squamous Cell Carcinoma 43 0.034
901
TRP009 Triple X Syndrome 42 0.034
902
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.034
903
ADR016 Adrenal Cortical Carcinoma 48 0.034
904
SYS071 Systemic Autoimmune Disease 37 0.034
905
ART109 Arterial Thoracic Outlet Syndrome 22 0.034
906
P MDL005 Medulloblastoma 77 0.034
907
P HLP001 Holoprosencephaly 68 0.034
908
HSH003 Hashimoto Thyroiditis 62 0.034
909
CRC021 Carcinosarcoma 61 0.034
910
P TST021 Testicular Germ Cell Tumor 61 0.034
911
P MNC007 Monocytic Leukemia 54 0.034
912
HRT012 Heart Valve Disease 53 0.034
913
ECH003 Echinococcosis 53 0.034
914
P LCT001 Lactic Acidosis 51 0.034
915
ADN009 Adenosquamous Carcinoma 49 0.034
916
QDR001 Quadriplegia 48 0.034
917
PLY150 Polykaryocytosis Inducer 31 0.034
918
P MTH008 Methylmalonic Acidemia 51 0.034
919
FCL012 Facial Paralysis 48 0.034
920
HST009 Histiocytoma 46 0.034
921
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.033
922
P DRM010 Dermatomyositis 61 0.033
923
DBT006 Diabetic Macular Edema 48 0.033
924
c LRG017 Large Intestine Cancer 47 0.033
925
KRT013 Keratolytic Winter Erythema 46 0.033
926
FBR003 Fibrous Histiocytoma 41 0.033
927
c RTN042 Retinitis Pigmentosa 12 40 0.033
928
c GLY008 Glycogen Storage Disease Ii 70 0.033
929
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.033
930
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.033
931
CMM005 Common Cold 56 0.033
932
P LCH002 Lichen Planus 54 0.033
933
P ANG015 Angioedema 54 0.033
934
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.033
935
ASP003 Aseptic Meningitis 51 0.033
936
BNN003 Bone Inflammation Disease 48 0.033
937
P TRT019 Torticollis 47 0.033
938
PHY002 Physical Disorder 42 0.033
939
MTR087 Maternal Uniparental Disomy 30 0.033
940
MGK001 Megakaryocytic Leukemia 64 0.033
941
P MTR012 Mitral Valve Disease 57 0.033
942
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.033
943
HYP458 Hyper Ige Syndrome 54 0.033
944
PTT009 Pituitary Gland Disease 54 0.033
945
INF034 Infective Endocarditis 52 0.033
946
MCR141 Mucormycosis 51 0.033
947
THY125 Thyroid Gland Medullary Carcinoma 51 0.033
948
c LRG001 Large Cell Carcinoma 49 0.033
949
KRT002 Keratomalacia 48 0.033
950
HRN026 Hernia, Hiatus 45 0.033
951
CRB086 Cerebral Aneurysms 40 0.033
952
PCD001 Pica Disease 37 0.033
953
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.033
954
c ART115 Aortic Valve Disease 1 75 0.032
955
P WSK001 Wiskott-Aldrich Syndrome 71 0.032
956
INT146 Intervertebral Disc Disease 62 0.032
957
TCK001 Tick-Borne Encephalitis 52 0.032
958
P LYM024 Lymphatic System Disease 48 0.032
959
CCN001 Cocaine Dependence 48 0.032
960
HYP016 Hypochondriasis 45 0.032
961
OBS003 Obsessive-Compulsive Personality Disorder 44 0.032
962
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.032
963
CNN005 Connective Tissue Disease 66 0.032
964
P NRV007 Nervous System Disease 66 0.032
965
P AGM001 Agammaglobulinemia 65 0.032
966
MSC007 Muscle Hypertrophy 63 0.032
967
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.032
968
CLL003 Cellulitis 54 0.032
969
c PRD040 Periodontitis, Chronic 54 0.032
970
P EPD016 Epidermolysis Bullosa 53 0.032
971
HMP001 Hemopericardium 46 0.032
972
MYF001 Myofibroma 42 0.032
973
YLL002 Yellow Fever 60 0.032
974
c CHR417 Chronic Graft Versus Host Disease 56 0.032
975
ERY004 Erysipelas 48 0.032
976
P OCY003 Oocyte Maturation Defect 1 45 0.032
977
NWC001 Newcastle Disease 44 0.032
978
ALX002 Alexithymia 39 0.032
979
PRM020 Premenstrual Tension 39 0.032
980
DPR002 Depersonalization Disorder 38 0.032
981
PRT049 Partial Deletion of Y 34 0.032
982
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.032
983
BRN028 Brain Cancer 73 0.032
984
PCK003 Pick Disease of Brain 68 0.032
985
MRK001 Merkel Cell Carcinoma 66 0.032
986
HYP020 Hyperprolactinemia 64 0.032
987
APH001 Aphthous Stomatitis 57 0.032
988
c ADL017 Adult T-Cell Leukemia 57 0.032
989
LST001 Listeriosis 54 0.032
990
c LKM070 Leukemia, Acute Monocytic 53 0.032
991
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.032
992
MNN009 Meningoencephalitis 49 0.032
993
BCT004 Bacteriuria 48 0.032
994
P PRC019 Precocious Puberty 47 0.032
995
ORC001 Orchitis 45 0.032
996
EXC002 Exocrine Pancreatic Insufficiency 41 0.032
997
P ESS003 Essential Thrombocythemia 67 0.031
998
c WLM013 Wilms Tumor 1 65 0.031
999
P ANT006 Antiphospholipid Syndrome 54 0.031
1000
P ICH004 Ichthyosis 54 0.031
1001
OST016 Osteochondrosis 53 0.031
1002
LYM022 Lymphangioma 53 0.031
1003
P PRC012 Pericardial Effusion 51 0.031
1004
VLV047 Volvulus of Midgut 50 0.031
1005
FBR009 Fibrous Dysplasia 48 0.031
1006
c OVR114 Ovarian Cancer 1 38 0.031
1007
c PRM196 Premature Ovarian Failure 1 68 0.031
1008
c ANM038 Anemia, Autoimmune Hemolytic 61 0.031
1009
P MLN069 Melanoma, Uveal 58 0.031
1010
URN010 Urinary Tract Obstruction 57 0.031
1011
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.031
1012
SPN041 Spinal Cord Disease 56 0.031
1013
SML019 Smallpox 56 0.031
1014
FML037 Female Breast Cancer 52 0.031
1015
PLR008 Pleurisy 51 0.031
1016
c INF145 Infantile Liver Failure Syndrome 1 50 0.031
1017
CRT013 Carotid Stenosis 50 0.031
1018
SNT005 Sinoatrial Node Disease 49 0.031
1019
CRN027 Corneal Neovascularization 47 0.031
1020
P FML187 Familial Hypertension 37 0.031
1021
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.031
1022
BRT054 Brittle Bone Disorder 70 0.030
1023
DGR001 Digeorge Syndrome 63 0.030
1024
BRS099 Breast Ductal Carcinoma 62 0.030
1025
PNM010 Pneumothorax, Primary Spontaneous 60 0.030
1026
INT066 Interstitial Lung Disease 59 0.030
1027
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.030
1028
FDB001 Foodborne Botulism 56 0.030
1029
CLR030 Clear Cell Renal Cell Carcinoma 53 0.030
1030
P HML001 Hemolytic-Uremic Syndrome 52 0.030
1031
SPS003 Spastic Diplegia 50 0.030
1032
c BSL024 Basal Cell Carcinoma 1 47 0.030
1033
c BCT013 Bacterial Pneumonia 47 0.030
1034
GST071 Gastrointestinal Carcinoma 45 0.030
1035
STS002 Situs Inversus 45 0.030
1036
ACN001 Acinar Cell Carcinoma 45 0.030
1037
P BLP003 Blepharospasm 44 0.030
1038
c BLP048 Blepharospasm, Benign Essential 37 0.030
1039
KRT019 Keratitis, Hereditary 67 0.030
1040
ACT200 Acute Monoblastic Leukemia 55 0.030
1041
CRD001 Cardiac Tamponade 46 0.030
1042
c RTN041 Retinitis Pigmentosa 11 41 0.030
1043
c MCR112 Microvascular Complications of Diabetes 2 41 0.030
1044
ATM052 Autoimmune Disease 1 37 0.030
1045
GRM010 Germ Cells Tumors 34 0.030
1046
P NRM002 Normal Pressure Hydrocephalus 56 0.029
1047
MTN003 Motion Sickness 52 0.029
1048
ANH002 Anhidrosis 46 0.029
1049
P SBR004 Seborrheic Dermatitis 45 0.029
1050
ADR004 Adrenal Cortical Adenocarcinoma 38 0.029
1051
c RNG005 Ring Chromosome 10 30 0.029
1052
TCK004 Tick Infestation 27 0.029
1053
c EXD008 Exudative Vitreoretinopathy 1 69 0.029
1054
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.029
1055
P BLD062 Bile Duct Cancer 65 0.029
1056
BLD131 Bladder Urothelial Carcinoma 61 0.029
1057
MCR013 Microphthalmia 60 0.029
1058
DCT002 Ductal Carcinoma in Situ 59 0.029
1059
P RST001 Restless Legs Syndrome 54 0.029
1060
CRH005 Crohn's Colitis 52 0.029
1061
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.029
1062
PPL018 Papillary Adenocarcinoma 46 0.029
1063
c INH020 Inherited Metabolic Disorder 46 0.029
1064
OLG001 Oligospermia 45 0.029
1065
MLG065 Malignant Fibroxanthoma 44 0.029
1066
P MST009 Mastocytosis 63 0.029
1067
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.029
1068
ANN002 Anencephaly 55 0.029
1069
CPL003 Capillary Leak Syndrome 55 0.029
1070
SHG001 Shigellosis 55 0.029
1071
P LRY044 Larynx Cancer 54 0.029
1072
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.029
1073
CCN002 Cocaine Abuse 48 0.029
1074
P NRV006 Nervous System Cancer 48 0.029
1075
RFT001 Rift Valley Fever 47 0.029
1076
c CNT033 Central Nervous System Cancer 46 0.029
1077
FNC007 Functioning Pituitary Adenoma 44 0.029
1078
BNM001 Bone Marrow Cancer 43 0.029
1079
PLY068 Polysubstance Abuse 43 0.029
1080
PTT003 Pituitary-Dependent Cushing's Disease