Search results for 15(S)-HPETE

2215 hits were found for 15(S)-HPETE

# Family MCID Name MIFTS Score
1
PRT014 Protein S Deficiency 44 0.246
2
P BRS047 Breast Cancer 97 0.177
3
c HPT016 Hepatitis B 59 0.168
4
c THR092 Thrombophilia Due to Thrombin Defect 73 0.167
5
SCH014 Schistosomiasis 57 0.164
6
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.163
7
HLX001 Helix Syndrome 47 0.161
8
P LKM002 Leukemia 68 0.160
9
LYM133 Lymphoma, Hodgkin, Classic 69 0.159
10
48X005 48,xyyy 39 0.159
11
47X002 47,xyy 49 0.156
12
P DRR001 Diarrhea 55 0.155
13
P MYL006 Myeloid Leukemia 60 0.155
14
P LVR013 Liver Disease 68 0.152
15
P BLD134 Bladder Cancer 79 0.152
16
P NRB001 Neuroblastoma 72 0.150
17
P THL005 Thalassemia 60 0.150
18
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.149
19
P LNG032 Lung Cancer 98 0.148
20
P LYM118 Lymphoma 68 0.147
21
P CLR023 Colorectal Cancer 99 0.146
22
DPR016 Depression 63 0.144
23
P ALZ034 Alzheimer Disease 88 0.143
24
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.141
25
CHR178 Chromosomal Triplication 35 0.140
26
P ADN016 Adenocarcinoma 64 0.140
27
ACT119 Acute Promyelocytic Leukemia 63 0.140
28
BRK010 Burkitt Lymphoma 67 0.137
29
MNT002 Mental Depression 58 0.135
30
c LKM061 Leukemia, Acute Myeloid 84 0.132
31
P HPT023 Hepatocellular Carcinoma 100 0.131
32
PRT037 Pertussis 65 0.130
33
P OVR042 Ovarian Cancer 88 0.130
34
P TRN020 Turner Syndrome 67 0.129
35
ATM095 Autoimmune Disease 62 0.129
36
CRH001 Crohn's Disease 74 0.128
37
P SCK005 Sickle Cell Disease 50 0.127
38
LVR012 Liver Cirrhosis 62 0.127
39
THR024 Thrombosis 57 0.127
40
DWN001 Down Syndrome 70 0.126
41
P UVT001 Uveitis 57 0.126
42
P LKM062 Leukemia, Acute Lymphoblastic 69 0.125
43
EWN003 Ewing Sarcoma 69 0.125
44
P HRP006 Herpes Simplex 65 0.123
45
P RTN024 Retinoblastoma 73 0.123
46
ADN018 Adenoma 59 0.122
47
HMN044 Human Immunodeficiency Virus Type 1 71 0.121
48
c FML008 Familial Retinoblastoma 53 0.120
49
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.120
50
HRW001 Hair Whorl 36 0.120
51
SCK003 Sickle Cell Anemia 74 0.120
52
ADL002 Adult Syndrome 70 0.118
53
P PRS040 Prostate Cancer 97 0.118
54
P MJR001 Major Depressive Disorder 68 0.118
55
P GST053 Gastric Cancer 83 0.117
56
P ATX030 Ataxia-Telangiectasia 82 0.116
57
TLN003 Telangiectasis 52 0.116
58
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.116
59
PNG002 Pain Agnosia 51 0.115
60
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.115
61
LNG099 Lung Disease 60 0.115
62
ISC004 Ischemia 58 0.115
63
c SVR001 Severe Acute Respiratory Syndrome 62 0.114
64
DNT012 Dental Caries 53 0.114
65
ALL026 Allergic Hypersensitivity Disease 62 0.114
66
P END033 Endocarditis 57 0.114
67
P INF037 Inflammatory Bowel Disease 54 0.113
68
P PRD006 Prader-Willi Syndrome 59 0.113
69
P KDN018 Kidney Disease 72 0.113
70
P THR015 Thrombophilia 51 0.112
71
P VSC007 Vascular Disease 63 0.111
72
DRM006 Dermatitis 61 0.109
73
P NTR004 Neutropenia 63 0.108
74
TYP007 Typhoid Fever 63 0.108
75
BRR014 Barrett Esophagus 65 0.108
76
OST012 Osteoarthritis 78 0.108
77
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.107
78
P HPT021 Hepatitis 67 0.107
79
CRB039 Cerebrovascular Disease 67 0.107
80
DFC004 Deficiency Anemia 70 0.106
81
GLL048 Glial Tumor 45 0.106
82
SPN035 Spindle Cell Sarcoma 53 0.106
83
P GLM045 Glioma 63 0.106
84
P CTR002 Cataract 60 0.105
85
P PRK057 Parkinson Disease, Late-Onset 78 0.105
86
CHL014 Cholera 59 0.105
87
c SYS001 Systemic Lupus Erythematosus 86 0.105
88
SQM006 Squamous Cell Carcinoma 60 0.105
89
P DBT009 Diabetes Mellitus 64 0.104
90
MLR004 Malaria 81 0.104
91
LPP008 Lipoprotein Quantitative Trait Locus 62 0.104
92
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.103
93
P PNC035 Pancreatic Cancer 84 0.103
94
P ANG001 Angelman Syndrome 69 0.103
95
c HYP595 Hypertension, Essential 84 0.102
96
MYL069 Myeloma, Multiple 85 0.102
97
SRC014 Sarcoma 65 0.102
98
c PRC016 Pre-Eclampsia 63 0.101
99
PLM033 Pulmonary Embolism 59 0.101
100
TXC005 Toxic Shock Syndrome 62 0.101
101
c PNS012 Paine Syndrome 61 0.100
102
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.100
103
PRP030 Purpura 54 0.100
104
c SML038 Small Cell Cancer of the Lung 65 0.100
105
HMP009 Haemophilus Influenzae 43 0.099
106
HMG005 Hemoglobinopathy 56 0.099
107
THY029 Thyroid Carcinoma 59 0.099
108
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.098
109
CHL068 Cholestasis 61 0.098
110
CHC001 Chickenpox 60 0.098
111
PRT036 Peritonitis 64 0.098
112
AST005 Asthma 76 0.098
113
P NRP001 Neuropathy 56 0.097
114
P SZR006 Seizure Disorder 56 0.097
115
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.097
116
STR067 Stroke, Ischemic 81 0.097
117
P INF032 Infertility 57 0.097
118
P HRT032 Heart Disease 75 0.097
119
GLB015 Glioblastoma Multiforme 75 0.096
120
P CHR345 Chronic Pain 44 0.096
121
OST159 Osteogenic Sarcoma 66 0.096
122
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.096
123
c BTT014 Beta-Thalassemia 74 0.096
124
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.095
125
P BCL017 B-Cell Lymphoma 58 0.095
126
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.095
127
CRV035 Cervical Cancer 76 0.095
128
ALC007 Alcohol Dependence 66 0.094
129
ULC004 Ulcerative Colitis 73 0.094
130
GST045 Gastroenteritis 59 0.094
131
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.094
132
P CRN300 Coronary Heart Disease 1 63 0.094
133
CYS001 Cystic Fibrosis 81 0.094
134
P TRM003 Tremor 54 0.093
135
P PSR002 Psoriasis 62 0.093
136
VCC001 Vaccinia 49 0.093
137
P LPS004 Lupus Erythematosus 61 0.092
138
P VSC011 Vasculitis 62 0.092
139
CYT002 Cytokine Deficiency 42 0.092
140
P MNN013 Meningitis 66 0.092
141
P MLN008 Melanoma 69 0.091
142
P THR014 Thrombocytopenia 67 0.091
143
PST011 Pustulosis of Palm and Sole 52 0.091
144
ANX010 Anxiety 73 0.091
145
IMM167 Immune Deficiency Disease 78 0.091
146
ATX019 Ataxia with Vitamin E Deficiency 42 0.091
147
P RHM011 Rheumatoid Arthritis 80 0.091
148
ENH001 Enhanced S-Cone Syndrome 57 0.090
149
P PNM007 Pneumonia 68 0.090
150
P SCL018 Scoliosis 60 0.089
151
P SLM003 Salmonellosis 55 0.089
152
CNG034 Congestive Heart Failure 69 0.089
153
VSL002 Visual Epilepsy 59 0.089
154
P INF038 Influenza 68 0.089
155
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.089
156
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.089
157
END086 End Stage Renal Disease 51 0.089
158
MSL001 Measles 62 0.088
159
ART140 Arteries, Anomalies of 52 0.088
160
TTN003 Tetanus 65 0.088
161
BRN024 Bronchitis 68 0.087
162
MYL009 Myelodysplastic Syndrome 70 0.086
163
HYP056 Hypoglycemia 66 0.086
164
c HPT073 Hepatitis C Virus 72 0.086
165
c RHB024 Rhabdomyosarcoma 2 67 0.086
166
P PLM037 Pulmonary Hypertension 67 0.086
167
c HPT003 Hepatitis a 62 0.086
168
P CRD119 Cardiac Arrest 67 0.086
169
DPH001 Diphtheria 60 0.085
170
HMC014 Homocysteinemia 53 0.085
171
BCT022 Bacterial Infectious Disease 56 0.085
172
END040 Endogenous Depression 55 0.085
173
SVR004 Severe Combined Immunodeficiency 73 0.085
174
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.085
175
P HYP265 Hypotonia 43 0.085
176
HNS001 Hansen's Disease 34 0.085
177
CVD001 Covid-19 44 0.085
178
P DMN002 Dementia 66 0.084
179
P EXN002 Exanthem 57 0.084
180
TRM010 Traumatic Brain Injury 51 0.084
181
c PRM038 Primary Agammaglobulinemia 44 0.084
182
P HYP086 Hypothyroidism 69 0.084
183
DSS009 Disseminated Intravascular Coagulation 57 0.084
184
c CHR684 Chronic Kidney Disease 70 0.084
185
P LPR021 Leprosy 3 69 0.083
186
HYP066 Hyperglycemia 61 0.083
187
P TRC086 Trichohepatoenteric Syndrome 1 62 0.082
188
LYM019 Lymphosarcoma 46 0.082
189
P ART022 Arthritis 69 0.082
190
c SPN225 Spondyloarthropathy 1 73 0.082
191
ANR007 Anorexia Nervosa 63 0.082
192
ACQ007 Acquired Immunodeficiency Syndrome 60 0.082
193
NRT001 Neurotic Disorder 53 0.082
194
HYP266 Hypoxia 57 0.082
195
P GLM007 Glomerulonephritis 57 0.082
196
FTT001 Fatty Liver Disease 61 0.082
197
c ACT073 Acute Leukemia 58 0.081
198
ANR040 Aneurysm 59 0.081
199
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.081
200
ESP021 Esophageal Cancer 90 0.081
201
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.081
202
CLT003 Colitis 62 0.081
203
PRS045 Prostatic Hypertrophy 53 0.081
204
P MYC007 Myocardial Infarction 70 0.081
205
P ENC018 Encephalopathy 61 0.081
206
P NPH012 Nephrotic Syndrome 60 0.080
207
MST005 Mastitis 53 0.080
208
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.079
209
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.079
210
c ACT075 Acute Myocardial Infarction 57 0.079
211
ATH013 Atherosclerosis Susceptibility 65 0.079
212
P ATS364 Autism 70 0.079
213
P ENC004 Encephalitis 61 0.079
214
BRN071 Brain Injury 49 0.079
215
SPL018 Splenomegaly 48 0.079
216
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.079
217
P ALC033 Alcohol Use Disorder 58 0.079
218
SKN016 Skin Disease 63 0.079
219
P RSP003 Respiratory Failure 74 0.079
220
c HYP836 Hypercholesterolemia, Familial, 1 73 0.079
221
P LTR001 Lateral Sclerosis 54 0.078
222
P HYP098 Hypereosinophilic Syndrome 67 0.078
223
ANG054 Angina Pectoris 66 0.078
224
P RBL001 Rubella 59 0.078
225
P MCR010 Microcephaly 59 0.078
226
OTT002 Otitis Media 72 0.078
227
P DRM053 Dermatitis, Atopic 66 0.078
228
P EPL164 Epilepsy 71 0.078
229
P SKN015 Skin Carcinoma 66 0.077
230
P HDC001 Headache 57 0.077
231
P HRS035 Hirschsprung Disease 1 65 0.077
232
P ESP024 Esophagitis 62 0.076
233
PRS021 Prostatic Adenoma 51 0.076
234
P PHC003 Pheochromocytoma 71 0.076
235
GST092 Gastroesophageal Reflux 67 0.076
236
INF034 Infective Endocarditis 53 0.076
237
PRT011 Protein C Deficiency 44 0.076
238
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.076
239
PLM001 Pulmonary Tuberculosis 69 0.076
240
P LKM071 Leukemia, Chronic Lymphocytic 79 0.075
241
P END044 Endometriosis 63 0.075
242
PLS011 Plasmacytoma 56 0.075
243
P RNG032 Ring Chromosome 42 0.075
244
BCK006 Back Pain 42 0.075
245
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.075
246
P MYP004 Myopathy 70 0.075
247
P MLT020 Multiple Sclerosis 72 0.075
248
RSC001 Rosacea 54 0.075
249
VLV047 Volvulus of Midgut 49 0.074
250
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.074
251
P ANR048 Aniridia 1 63 0.074
252
THR013 Thoracic Outlet Syndrome 54 0.074
253
FBR047 Fibromyalgia 58 0.074
254
P SYP003 Syphilis 58 0.074
255
c MGR028 Migraine with or Without Aura 1 67 0.074
256
P PRD008 Periodontitis 64 0.074
257
LSH001 Leishmaniasis 63 0.073
258
P KLZ004 Kala-Azar 1 41 0.073
259
IRN002 Iron Metabolism Disease 57 0.073
260
OST017 Osteomyelitis 64 0.073
261
TRN018 Transitional Cell Carcinoma 56 0.073
262
LPD008 Lipid Metabolism Disorder 62 0.073
263
IMP005 Impotence 52 0.073
264
ADR040 Adrenal Gland Pheochromocytoma 46 0.073
265
ORL011 Oral Cancer 60 0.073
266
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.073
267
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.073
268
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.073
269
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.073
270
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.073
271
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.073
272
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.073
273
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.073
274
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.073
275
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.073
276
c HPT001 Hepatitis C 62 0.073
277
P AST007 Astrocytoma 51 0.073
278
PLM031 Poliomyelitis 64 0.073
279
P ECL001 Eclampsia 50 0.073
280
ACN002 Acanthosis Nigricans 60 0.073
281
c ATR087 Atrial Standstill 1 75 0.073
282
PRS129 Prostatic Hyperplasia, Benign 49 0.073
283
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.072
284
OCL069 Ocular Motor Apraxia 51 0.072
285
DYS073 Dysphagia 50 0.072
286
HRT011 Heart Septal Defect 50 0.072
287
BRR002 Barrett's Adenocarcinoma 36 0.072
288
STM007 Stomatitis 50 0.072
289
END057 Endometrial Cancer 74 0.072
290
NTR005 Nutritional Deficiency Disease 62 0.072
291
AGN016 Aging 56 0.072
293
P HNT016 Huntington Disease 72 0.072
294
c BRN108 Branchiootic Syndrome 1 62 0.071
295
PPT005 Peptic Ulcer Disease 59 0.071
296
ERY051 Erythroleukemia, Familial 56 0.071
298
ATX010 Ataxia Neuropathy Spectrum 34 0.071
299
ACT064 Acute Necrotizing Encephalitis 33 0.071
300
BLD137 Blood Group--Ahonen 16 0.071
301
c BSL007 Basal Cell Carcinoma 68 0.071
302
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.071
303
P SRC025 Sarcoidosis 1 70 0.071
304
P BPL003 Bipolar Disorder 56 0.070
305
P RTN016 Retinal Degeneration 53 0.070
306
P CRD246 Cardiovascular System Disease 57 0.070
307
c MCR113 Microvascular Complications of Diabetes 3 52 0.070
308
c ACT068 Acute Cystitis 63 0.070
309
P FBR017 Fibrosarcoma 56 0.070
310
c ALP101 Alpha-Thalassemia 62 0.070
311
P MCR115 Microvascular Complications of Diabetes 5 66 0.069
312
P SCH015 Schizophrenia 74 0.069
313
DSS008 Disease of Mental Health 58 0.069
314
c MJR024 Major Affective Disorder 9 41 0.069
315
c MJR022 Major Affective Disorder 8 38 0.069
316
c ACT027 Acute Pancreatitis 60 0.068
317
CHL079 Children's Interstitial Lung Disease 26 0.068
318
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.068
319
c LKM005 Leukemia, T-Cell, Chronic 34 0.068
320
P LNG064 Lung Cancer Susceptibility 3 78 0.068
321
PPL052 Papillomatosis, Confluent and Reticulated 33 0.068
322
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.068
323
P PLM036 Pulmonary Fibrosis 65 0.068
324
c MCR120 Microvascular Complications of Diabetes 7 47 0.068
325
c MCR130 Microvascular Complications of Diabetes 6 41 0.068
326
c MCR133 Microvascular Complications of Diabetes 4 41 0.068
327
c FNC043 Fanconi Anemia, Complementation Group E 62 0.068
328
ARG004 Argyria 27 0.068
330
P THY032 Thyroiditis 52 0.067
331
P MSC005 Muscular Dystrophy 66 0.067
332
P HMP007 Hemophilia 51 0.067
333
P RHN004 Rhinitis 57 0.067
334
KPS004 Kaposi Sarcoma 75 0.067
335
P APL001 Aplastic Anemia 74 0.067
336
PPL022 Papilloma 54 0.066
337
P NSP012 Nasopharyngeal Carcinoma 66 0.066
338
RHM001 Rheumatic Fever 60 0.066
339
c DLT002 Dilated Cardiomyopathy 79 0.066
340
CRD132 Cardiac Conduction Defect 58 0.066
341
P HYP076 Hyperthyroidism 55 0.066
342
c ATS007 Autism Spectrum Disorder 67 0.066
343
P ATR011 Atrial Fibrillation 66 0.066
344
P PRS038 Personality Disorder 65 0.066
345
ADP007 Adie Pupil 39 0.065
346
P OVR082 Overgrowth Syndrome 50 0.065
347
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.065
348
BNR002 Bone Resorption Disease 48 0.065
349
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.065
350
GST023 Gastric Ulcer 53 0.065
351
P GRF003 Graft-Versus-Host Disease 72 0.065
352
SPN186 Spinal Cord Injury 60 0.065
353
c ACT071 Acute Kidney Failure 60 0.065
354
P HYP061 Hypertrophic Cardiomyopathy 70 0.065
355
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.065
356
P HYP069 Hyperparathyroidism 63 0.065
357
P PLY019 Polyneuropathy 56 0.065
358
DFF005 Diffuse Large B-Cell Lymphoma 55 0.064
359
P OPN001 Open-Angle Glaucoma 49 0.064
360
c PCH010 Pachyonychia Congenita 3 44 0.064
361
P GST044 Gastritis 56 0.064
362
P CHL066 Cholangitis 51 0.064
363
PSY004 Psychotic Disorder 67 0.064
364
CHL123 Chlamydia 59 0.064
365
P PRP034 Purpura Fulminans 43 0.064
366
AMN003 Amnestic Disorder 54 0.064
367
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.064
368
DYS015 Dysentery 52 0.064
369
CHL065 Cholangiocarcinoma 68 0.064
370
ORL015 Oral Squamous Cell Carcinoma 43 0.064
371
P KDN017 Kidney Cancer 60 0.064
372
IGR001 Ige Responsiveness, Atopic 59 0.063
373
ATS010 Autosomal Recessive Disease 48 0.063
374
P RHB003 Rhabdomyosarcoma 63 0.063
375
c NRF023 Neurofibromatosis, Type Ii 80 0.063
376
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.063
377
P MMP001 Mumps 58 0.063
378
HRP004 Herpes Zoster 60 0.063
379
CHG001 Chagas Disease 66 0.063
380
SQM002 Squamous Cell Papilloma 46 0.063
381
HNM002 Hinman Syndrome 27 0.063
382
P HYD006 Hydrocephalus 66 0.062
383
P FML011 Familial Adenomatous Polyposis 72 0.062
384
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.062
385
P CNR004 Cone-Rod Dystrophy 2 73 0.062
386
P DYS154 Dystonia 65 0.062
387
APH002 Aphasia 57 0.062
388
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.062
389
P INS002 in Situ Carcinoma 53 0.062
390
CRH005 Crohn's Colitis 53 0.062
391
P PRP019 Peripheral Nervous System Disease 58 0.062
392
HPT082 Hepatic Adenomas, Familial 44 0.062
393
VRC005 Varicose Veins 60 0.062
394
PHR003 Pharyngitis 57 0.062
395
INT079 Intrahepatic Cholangiocarcinoma 51 0.062
396
P HMN010 Hemangioma 61 0.062
397
ONC002 Onchocerciasis 52 0.061
398
TBC004 Tobacco Addiction 64 0.061
399
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.061
400
P MYS005 Myositis 56 0.061
401
P VNT002 Ventricular Septal Defect 60 0.061
402
HDN002 Head Injury 46 0.061
403
P MSC003 Muscular Atrophy 52 0.061
404
P DDN001 Duodenal Ulcer 52 0.061
405
INT007 Intermediate Coronary Syndrome 55 0.061
406
c VRL010 Viral Hepatitis 52 0.061
407
P BNG032 Benign Mesothelioma 46 0.061
408
P ANT006 Antiphospholipid Syndrome 55 0.061
409
OST003 Osteonecrosis 61 0.061
410
P TXP001 Toxoplasmosis 60 0.061
411
CNS004 Constipation 58 0.061
412
INS024 Insulin-Like Growth Factor I 79 0.061
413
KHL003 Kohlschutter-Tonz Syndrome 65 0.061
414
OVR094 Ovarian Epithelial Cancer 38 0.061
415
MDD011 Mood Disorder 62 0.060
416
SFT003 Soft Tissue Sarcoma 56 0.060
417
P AMY004 Amyloidosis 70 0.060
418
INT017 Intestinal Schistosomiasis 48 0.060
419
MDD018 Middle East Respiratory Syndrome 43 0.059
420
SPN051 Spondylitis 51 0.059
421
P MYP006 Myopia 55 0.059
422
AMN001 Amenorrhea 54 0.059
423
HMS001 Hemosiderosis 54 0.059
424
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.059
425
P MLN007 Male Infertility 55 0.059
426
CRB004 Cerebral Artery Occlusion 45 0.059
427
EYD002 Eye Disease 58 0.059
428
IDP070 Idiopathic Scoliosis 42 0.059
429
CLF027 Cleft Palate, Isolated 64 0.059
430
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.059
431
P TRT010 Teratoma 52 0.058
432
P OST002 Osteoporosis 74 0.058
433
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.058
434
c SCL052 Scleroderma, Familial Progressive 61 0.058
435
INF009 Inflammatory Spondylopathy 31 0.058
436
P SLP006 Sleep Apnea 69 0.058
437
ALL003 Allergic Rhinitis 67 0.058
438
GST040 Gastric Adenocarcinoma 70 0.058
439
ART016 Aortic Aneurysm 69 0.058
440
P AXN002 Axenfeld-Rieger Syndrome 59 0.058
441
P HML002 Hemolytic Anemia 63 0.058
442
P CYS018 Cystitis 59 0.058
443
ANT024 Anthrax Disease 58 0.058
444
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.057
445
PRT013 Portal Hypertension 59 0.057
446
CNN005 Connective Tissue Disease 68 0.057
447
RCK004 Rickets 68 0.057
448
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.057
449
ENT011 Enterocolitis 51 0.057
450
P NRF002 Neurofibromatosis 56 0.057
451
SYN036 Syncope 45 0.057
452
P RRH023 Rare Hereditary Hemochromatosis 41 0.057
453
HYP080 Hypogonadism 50 0.057
454
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.057
455
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.057
456
P PNC044 Pancreatitis 61 0.057
457
ALL006 Allergic Asthma 56 0.057
458
P SPP010 Suppressor of Tumorigenicity 3 51 0.057
459
P CND004 Candidiasis 58 0.056
460
c DBT099 Diabetes Mellitus, Type I 65 0.056
461
c INF071 Inflammatory Bowel Disease 1 67 0.056
462
PLY150 Polykaryocytosis Inducer 31 0.056
463
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.056
464
SMN007 Seminoma 43 0.056
465
AND002 Androgen Insensitivity Syndrome 66 0.056
466
PRT018 Portal Vein Thrombosis 50 0.056
467
WLL004 Wallerian Degeneration 39 0.056
468
P SBS003 Substance Abuse 55 0.055
469
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.055
470
GT001 Gout 64 0.055
471
PNC001 Pancytopenia 54 0.055
472
NNL006 Non-Alcoholic Steatohepatitis 54 0.055
473
INT075 Intracranial Hypertension 53 0.055
474
PRP027 Peripheral Vascular Disease 71 0.055
475
CRB037 Cerebral Palsy 69 0.055
476
c WLM018 Wilms Tumor 5 61 0.055
477
ALL014 Allergic Encephalomyelitis 38 0.055
478
PNM008 Pneumothorax 56 0.055
479
P RCT021 Rectum Cancer 52 0.055
480
P MYS003 Myasthenia Gravis 68 0.055
481
ALR002 Al-Raqad Syndrome 33 0.054
482
PST053 Postherpetic Neuralgia 40 0.054
483
ETN001 Eating Disorder 60 0.054
484
PTH003 Pathologic Nystagmus 52 0.054
485
P MDL005 Medulloblastoma 77 0.054
486
ENT004 Enthesopathy 49 0.054
487
P ASP006 Aspergillosis 69 0.054
488
P ART023 Arthropathy 62 0.054
489
P BRN022 Bronchiectasis 59 0.054
490
TRY001 Trypanosomiasis 50 0.053
491
P NGH001 Night Blindness 48 0.053
492
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.053
493
CYT008 Cytomegalovirus Infection 57 0.053
494
P INT070 Intestinal Obstruction 58 0.053
495
P ALP106 Alport Syndrome 1, X-Linked 55 0.053
496
CLF001 Cleft Lip 53 0.053
497
SPT004 Septic Arthritis 58 0.053
498
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.053
499
HLC007 Helicobacter Pylori Infection 59 0.053
500
KRT019 Keratitis, Hereditary 65 0.053
501
RHM028 Rheumatic Heart Disease 53 0.053
502
c MNN043 Meningioma, Familial 74 0.053
503
ANX004 Anoxia 40 0.053
504
TRN015 Transient Cerebral Ischemia 63 0.053
505
P SML001 Small Cell Carcinoma 52 0.053
506
P MYC008 Myocarditis 59 0.052
507
P TBR001 Tuberous Sclerosis 70 0.052
508
FSC004 Fasciitis 50 0.052
509
CLN015 Colon Adenocarcinoma 65 0.052
510
P LRY044 Larynx Cancer 55 0.052
511
P PRP029 Porphyria 62 0.052
512
PST092 Posttransplant Acute Limbic Encephalitis 29 0.052
513
P TTR001 Tetralogy of Fallot 70 0.052
514
P SYS005 Systemic Scleroderma 68 0.052
515
c FNC027 Fanconi Anemia, Complementation Group a 81 0.052
516
PTT037 Pituitary Tumors 44 0.052
517
LPT014 Leptin Deficiency or Dysfunction 74 0.052
518
GST033 Gestational Diabetes 61 0.052
519
MCS002 Mucositis 56 0.052
520
LWC001 Low Compliance Bladder 43 0.052
521
MNN042 Meningioma, Radiation-Induced 62 0.051
522
SPN021 Spinal Meningioma 50 0.051
523
THR016 Thrombophlebitis 51 0.051
524
ERY003 Erythema Multiforme 58 0.051
525
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.051
526
P ART021 Arteriosclerosis 54 0.051
527
URM002 Uremia 49 0.051
528
P MYC084 Mycobacterium Tuberculosis 1 68 0.051
529
P END047 Endophthalmitis 53 0.051
530
P URT039 Urticaria 58 0.051
531
c ACT134 Acute Liver Failure 56 0.051
532
P PTS002 Ptosis 53 0.051
533
c GLC092 Glaucoma, Primary Open Angle 62 0.051
534
P PRM006 Primary Biliary Cirrhosis 62 0.051
535
P PLY018 Polycythemia 56 0.051
536
GLC003 Glucose Intolerance 54 0.051
537
CLL003 Cellulitis 54 0.051
538
PPT001 Peptic Esophagitis 52 0.051
539
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.051
540
HYD002 Hydronephrosis 60 0.051
541
P GLL022 Guillain-Barre Syndrome 59 0.051
542
c DWL002 Dowling-Degos Disease 1 58 0.051
543
KRT009 Keratosis 51 0.050
544
INT066 Interstitial Lung Disease 60 0.050
545
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.050
546
SCR001 Secretory Meningioma 41 0.050
547
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
548
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.050
549
LYM017 Lyme Disease 64 0.050
550
P MVM001 Movement Disease 63 0.050
551
P SCL057 Scoliosis, Isolated 1 41 0.050
552
c EXD008 Exudative Vitreoretinopathy 1 71 0.050
553
ECH003 Echinococcosis 53 0.050
554
SVR097 Severe Cutaneous Adverse Reaction 69 0.050
555
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.050
556
PRP016 Paraplegia 52 0.050
557
FLR002 Filariasis 55 0.050
558
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.050
559
c GLL024 Gallbladder Disease 1 53 0.050
560
P FRD001 Friedreich Ataxia 64 0.049
561
NRL016 Neural Tube Defects 82 0.049
562
GTR002 Goiter 53 0.049
563
SKN019 Skin Melanoma 68 0.049
564
P STR020 Strabismus 55 0.049
565
MCH006 Mechanical Strabismus 42 0.049
566
CRN030 Coronary Stenosis 50 0.049
567
SBC016 Subacute Delirium 44 0.049
568
P HYP750 Hypertriglyceridemia, Familial 62 0.049
569
c PST005 Posterior Uveitis 54 0.049
570
HRL004 Hurler-Scheie Syndrome 55 0.049
571
MYF002 Myofascial Pain Syndrome 42 0.049
572
P ALP008 Alopecia 54 0.049
573
RYN005 Raynaud Phenomenon 47 0.049
574
P CLC063 Celiac Disease 1 66 0.048
575
CNT047 Contact Dermatitis 58 0.048
576
PLS009 Plasma Cell Neoplasm 51 0.048
577
P PLY011 Polycystic Ovary Syndrome 56 0.048
578
WST005 West Nile Virus 54 0.048
579
CHL004 Cholelithiasis 49 0.048
580
c ACT135 Acute Graft Versus Host Disease 52 0.048
581
ERY066 Erythema Multiforme Major 30 0.048
582
BRC012 Brucellosis 64 0.048
583
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.048
584
HPT022 Hepatoblastoma 56 0.048
585
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.048
586
LYM040 Lymphoblastic Lymphoma 54 0.048
587
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.048
588
PLG002 Plague 63 0.048
589
P PLY014 Polycystic Kidney Disease 62 0.048
590
P LMY004 Leiomyosarcoma 63 0.048
591
PSR001 Psoriatic Arthritis 61 0.048
592
P ADL017 Adult T-Cell Leukemia 56 0.048
593
SCH036 Scheie Syndrome 72 0.047
594
P HMC002 Homocystinuria 53 0.047
595
P CNJ013 Conjunctivitis 65 0.047
596
ILS001 Ileus 51 0.047
597
PHN003 Phenylketonuria 75 0.047
598
APP008 Appendicitis 61 0.047
599
DBL002 Double Outlet Right Ventricle 56 0.047
600
ACT084 Acute Stress Disorder 47 0.047
601
KRT013 Keratolytic Winter Erythema 46 0.047
602
P BND020 Bone Disease 59 0.047
603
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.047
604
ALB002 Albinism 46 0.047
605
P AVS003 Avascular Necrosis 42 0.047
606
c ATM011 Autoimmune Hepatitis 63 0.047
607
P PNC025 Panic Disorder 53 0.047
608
P THY023 Thymoma 65 0.047
609
CHL067 Cholecystitis 57 0.047
610
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.047
611
P GRV001 Graves' Disease 55 0.047
612
HRT012 Heart Valve Disease 53 0.047
613
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.047
614
ING001 Inguinal Hernia 60 0.047
615
PLM010 Pulmonary Edema 54 0.047
616
P GLL018 Gallbladder Cancer 57 0.047
617
CTN007 Cutaneous Leishmaniasis 62 0.047
618
P MTR003 Mitral Valve Stenosis 50 0.047
619
ART001 Arterial Tortuosity Syndrome 66 0.047
620
NSS002 Neisseria Meningitidis Infection 47 0.047
621
P DBT005 Diabetes Insipidus 55 0.047
622
P FLL037 Follicular Lymphoma 67 0.046
623
c MLG084 Malignant Fibrous Histiocytoma 63 0.046
624
NND010 Nondisjunction 34 0.046
625
PLS007 Plasmodium Falciparum Malaria 52 0.046
626
AZS001 Azoospermia 50 0.046
627
KWS002 Kawasaki Disease 65 0.046
628
CLR108 Colorectal Adenoma 64 0.046
629
PST028 Post-Traumatic Stress Disorder 58 0.046
630
HYP005 Hypokalemia 55 0.046
631
NRT004 Neuritis 52 0.046
632
P MMB011 Membranous Nephropathy 50 0.046
633
GNG013 Gingivitis 59 0.046
634
RBS001 Rabies 58 0.046
635
MCL006 Macular Retinal Edema 55 0.046
636
IRD001 Iridocyclitis 53 0.046
637
YLL002 Yellow Fever 61 0.046
638
HND015 Hand Skill, Relative 33 0.046
639
P DNG005 Dengue Virus 59 0.046
640
c THY107 Thymoma, Familial 52 0.046
641
LMY002 Leiomyoma 52 0.046
642
49X006 49, Xxxxy Syndrome 41 0.046
643
SHG001 Shigellosis 60 0.046
644
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.046
645
P SLP005 Sleep Disorder 59 0.046
646
P SNS001 Sensorineural Hearing Loss 60 0.046
647
P PYL005 Pyelonephritis 56 0.046
648
PRC013 Pericarditis 54 0.046
649
c HMP029 Hemophilia a 67 0.045
650
CCC001 Coccidioidomycosis 58 0.045
651
LNG031 Lung Benign Neoplasm 51 0.045
652
SYN007 Synovitis 54 0.045
653
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.045
654
PLC002 Plica Syndrome 36 0.045
655
HYP748 Hypertelorism 50 0.045
656
OBS002 Obsessive-Compulsive Disorder 68 0.045
657
P NRV007 Nervous System Disease 66 0.045
658
P ANP001 Anaplastic Large Cell Lymphoma 58 0.045
659
P GND004 Gonadal Dysgenesis 48 0.045
660
VSC002 Vascular Dementia 57 0.045
661
SLP001 Sleeping Sickness 54 0.045
662
PFF001 Pfeiffer Syndrome 79 0.045
663
PLY001 Polycythemia Vera 69 0.045
664
CRD137 Cardiogenic Shock 47 0.045
665
BLR008 Bilirubin Metabolic Disorder 57 0.045
666
FDL002 Food Allergy 51 0.045
667
VTM033 Vitamin K Deficiency Bleeding 48 0.045
668
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.045
669
SCB001 Scabies 50 0.045
670
TST014 Testicular Cancer 46 0.045
671
P CRN037 Craniosynostosis 68 0.044
672
INS001 Insulinoma 60 0.044
673
MNN009 Meningoencephalitis 49 0.044
674
ART002 Arts Syndrome 64 0.044
675
BRN056 Bronchopulmonary Dysplasia 57 0.044
676
GRN017 Granulocytopenia 44 0.044
677
c FML001 Familial Atrial Fibrillation 65 0.044
678
P ART005 Arteriovenous Malformation 65 0.044
679
CHR074 Choriocarcinoma 47 0.044
680
RFR003 Refractive Error 43 0.044
681
c FML035 Familial Hyperlipidemia 55 0.044
682
ART074 Aortic Dissection 52 0.044
683
c HMP004 Hemophilia B 68 0.044
684
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.044
685
HST010 Histiocytosis 48 0.044
686
PRN019 Perinatal Necrotizing Enterocolitis 59 0.044
687
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.044
688
ATR057 Atrioventricular Block 55 0.044
689
PLC008 Placenta Disease 50 0.043
690
AST006 Astigmatism 47 0.043
691
KRT002 Keratomalacia 47 0.043
692
FCL012 Facial Paralysis 46 0.043
693
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.043
694
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.043
695
BRN004 Brain Edema 56 0.043
696
VRL011 Viral Infectious Disease 61 0.043
697
DCT002 Ductal Carcinoma in Situ 59 0.043
698
GST010 Gestational Trophoblastic Neoplasm 46 0.043
699
c CHR064 Chronic Monocytic Leukemia 33 0.043
700
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.043
701
MYL005 Myelofibrosis 70 0.043
702
NRL005 Neurilemmoma 60 0.043
703
ANS003 Anisakiasis 40 0.043
704
P RTN022 Retinal Vein Occlusion 53 0.043
705
VRC001 Varicocele 49 0.043
706
ACR007 Acromegaly 71 0.042
707
CRC021 Carcinosarcoma 62 0.042
708
HMP005 Hemiplegia 55 0.042
709
HYP014 Hyperuricemia 52 0.042
710
P CHN012 Chondrosarcoma 56 0.042
711
c HMC039 Hemochromatosis, Type 1 74 0.042
712
P OPT009 Optic Neuritis 57 0.042
713
HYP060 Hyperinsulinism 54 0.042
714
P EPD016 Epidermolysis Bullosa 53 0.042
715
P DVL012 Developmental Dysplasia of the Hip 1 38 0.042
716
P ADL010 Adult Respiratory Distress Syndrome 65 0.042
717
BCT004 Bacteriuria 49 0.042
718
c JVN010 Juvenile Rheumatoid Arthritis 64 0.042
719
P MTC069 Mitochondrial Disorders 56 0.042
720
TTR011 Tetraploidy 47 0.042
721
WRN001 Werner Syndrome 69 0.042
722
DCB001 Decubitus Ulcer 61 0.042
723
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.042
724
AVN001 Avian Influenza 59 0.042
725
PLR007 Pleural Empyema 50 0.042
726
SXL003 Sexual Disorder 47 0.042
727
P SPN046 Spinal Muscular Atrophy 62 0.042
728
MRF001 Marfan Syndrome 77 0.042
729
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.042
730
STT001 Status Epilepticus 60 0.041
731
P PMP001 Pemphigus 54 0.041
732
SPN019 Spondylolisthesis 51 0.041
733
NCR007 Necrotizing Fasciitis 48 0.041
734
PYD002 Pyoderma 50 0.041
735
NPH009 Nephrolithiasis 55 0.041
736
PPL002 Papillary Carcinoma 47 0.041
737
SPS057 Spasticity 45 0.041
738
MYC088 Mycobacterium Avium Complex Infections 29 0.041
739
AND005 Androgen Insensitivity Syndrome, Mild 19 0.041
740
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.041
741
c HPT015 Hepatitis D 49 0.041
742
BDD001 Budd-Chiari Syndrome 63 0.041
743
P SJG008 Sjogren Syndrome 61 0.041
744
EMB004 Embryonal Carcinoma 56 0.041
745
PLY100 Polyploidy 40 0.041
746
c OVR114 Ovarian Cancer 1 38 0.041
747
PNC129 Pancreatic Adenocarcinoma 68 0.041
748
P MLN069 Melanoma, Uveal 59 0.041
749
c ART101 Aortic Valve Disease 2 65 0.040
750
c WLM013 Wilms Tumor 1 65 0.040
751
LMB062 Limb Ischemia 55 0.040
752
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.040
753
DMY004 Demyelinating Disease 52 0.040
754
CRV045 Cervical Intraepithelial Neoplasia 39 0.040
755
KRN002 Kearns-Sayre Syndrome 63 0.040
756
CYN002 Cyanosis, Transient Neonatal 45 0.040
757
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.040
758
P PLY006 Polydactyly 59 0.040
759
c PRM005 Primary Hyperparathyroidism 58 0.040
760
FLR001 Filarial Elephantiasis 55 0.040
761
P PLM034 Pulmonary Emphysema 55 0.040
762
KRT006 Keratoconjunctivitis 53 0.040
763
P HYP040 Hypospadias 51 0.040
764
c MLG068 Malignant Glioma 46 0.040
765
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.040
766
c DNG003 Dengue Disease 59 0.040
767
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 28 0.040
768
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.040
769
MTH009 Mouth Disease 56 0.040
770
P MNC007 Monocytic Leukemia 53 0.040
771
RTN001 Retinal Vasculitis 47 0.040
772
BNG077 Benign Idiopathic Neonatal Seizures 26 0.040
773
MSC157 Muscular Dystrophy, Duchenne Type 72 0.040
774
c PRS136 Prostate Cancer, Hereditary, 6 33 0.040
775
c PRS130 Prostate Cancer, Hereditary, 8 32 0.040
776
CRT013 Carotid Stenosis 50 0.039
777
P TMP001 Temporal Lobe Epilepsy 50 0.039
778
FSC002 Fascioliasis 42 0.039
779
c MST023 Mesothelioma, Malignant 57 0.039
780
VSC003 Visceral Leishmaniasis 55 0.039
781
c BCT007 Bacterial Meningitis 55 0.039
782
PRP080 Peripheral Artery Disease 53 0.039
783
THR004 Thrombocytosis 51 0.039
784
HPT004 Hepatic Coma 45 0.039
785
P MTR014 Motor Neuron Disease 65 0.039
786
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.039
787
CYS005 Cysticercosis 53 0.039
788
P PRN023 Prion Disease 57 0.039
789
c HMG029 Hemoglobin Se Disease 39 0.039
790
STN013 Stenotrophomonas Maltophilia Infection 25 0.039
791
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.039
792
THY111 Thyroid Carcinoma, Familial Medullary 67 0.039
793
THY030 Thyroid Gland Disease 52 0.039
794
SPS019 Spastic Paraparesis 38 0.039
795
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.039
796
HSH003 Hashimoto Thyroiditis 62 0.039
797
THY122 Thyroid Gland Cancer 57 0.039
798
TRC023 Trichinosis 53 0.039
799
c SCN007 Secondary Hyperparathyroidism 51 0.039
800
CHR078 Chorioretinitis 50 0.039
801
LPR001 Lepromatous Leprosy 50 0.039
802
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.039
803
SCR015 Scarlet Fever 39 0.039
804
MTY003 Mutyh Polyposis 30 0.039
805
LYM009 Lymphocytic Choriomeningitis 47 0.038
806
LKP003 Leukoplakia 39 0.038
807
P KRT007 Keratoconus 50 0.038
808
P ART018 Aortic Valve Insufficiency 49 0.038
809
CMP010 Complex Regional Pain Syndrome 58 0.038
810
BRN002 Bronchiolitis 59 0.038
811
ANK001 Ankylosis 51 0.038
812
c MTR002 Mitral Valve Insufficiency 48 0.038
813
NRG002 Neurogenic Bladder 55 0.038
814
INT051 Intussusception 53 0.038
815
P PLV020 Pelvic Organ Prolapse 57 0.038
816
P MYM013 Moyamoya Disease 1 57 0.038
817
P HML001 Hemolytic-Uremic Syndrome 53 0.038
818
c INH030 Inherited Retinal Disorder 51 0.038
819
DWR001 Dwarfism 44 0.038
820
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.038
821
MTB004 Metabolic Acidosis 50 0.037
822
MCR004 Macroglobulinemia 49 0.037
823
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.037
824
ALL010 Allergic Contact Dermatitis 56 0.037
825
OCL006 Ocular Hypertension 53 0.037
826
ACT017 Acute Chest Syndrome 51 0.037
827
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.037
828
P FML018 Familial Mediterranean Fever 73 0.037
829
P ORT004 Orthostatic Intolerance 62 0.037
830
INT002 Intermittent Claudication 61 0.037
831
IRN001 Iron Deficiency Anemia 59 0.037
832
P PRC019 Precocious Puberty 46 0.037
833
TTH006 Tooth Disease 46 0.037
834
P MYC033 Myoclonus 46 0.037
835
URL001 Urolithiasis 45 0.037
836
c MCR129 Microvascular Complications of Diabetes 1 66 0.037
837
P CCK001 Cockayne Syndrome 66 0.037
838
BRS099 Breast Ductal Carcinoma 62 0.037
839
P EHL001 Ehlers-Danlos Syndrome 58 0.037
840
TNS005 Tonsillitis 57 0.037
841
AVD001 Avoidant Personality Disorder 51 0.037
842
c SVR005 Severe Pre-Eclampsia 50 0.037
843
OPT003 Opiate Dependence 50 0.037
844
ADR016 Adrenal Cortical Carcinoma 48 0.037
845
c INH020 Inherited Metabolic Disorder 47 0.037
846
CRT015 Carotid Artery Occlusion 45 0.037
847
c BCT013 Bacterial Pneumonia 48 0.037
848
P PRG013 Paraganglioma 52 0.037
849
FBR054 Fibroma 44 0.037
850
P RRT020 Rare Tumor 41 0.037
851
P MLT074 Multiple Endocrine Neoplasia 56 0.036
852
P CRC039 Coarctation of Aorta 47 0.036
853
P ATR010 Atrial Heart Septal Defect 60 0.036
854
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.036
855
P GLM040 Glioma Susceptibility 1 81 0.036
856
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.036
857
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.036
858
P HRD011 Hereditary Spherocytosis 60 0.036
859
INC002 Inclusion Body Myositis 58 0.036
860
VTM002 Vitamin B12 Deficiency 48 0.036
861
P BNG030 Benign Ependymoma 60 0.036
862
HPT019 Hepatic Encephalopathy 60 0.036
863
SCH003 Schizophreniform Disorder 56 0.036
864
PRS047 Prostatitis 56 0.036
865
SLC006 Silicosis 56 0.036
866
NRN004 Neuroendocrine Tumor 55 0.036
867
CLL010 Cellular Ependymoma 54 0.036
868
P RNL017 Renal Oncocytoma 53 0.036
869
CHR073 Choreatic Disease 52 0.036
870
OST011 Osteomalacia 52 0.036
871
P CMP008 Compartment Syndrome 49 0.036
872
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.036
873
ATN005 Autonomic Dysfunction 46 0.036
874
IRR002 Irritable Bowel Syndrome 65 0.036
875
GLS018 Glass Syndrome 57 0.036
876
FND002 Fundus Dystrophy 55 0.036
877
P FRG001 Fragile X Syndrome 70 0.036
878
MNT001 Mantle Cell Lymphoma 69 0.036
879
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.036
880
LGN006 Legionnaire Disease 52 0.036
881
THY125 Thyroid Gland Medullary Carcinoma 50 0.036
882
LRN003 Learning Disability 49 0.036
883
BNN003 Bone Inflammation Disease 48 0.036
884
KLD004 Keloid Disorder 40 0.036
885
CHL039 Choledocholithiasis 38 0.036
886
CLR030 Clear Cell Renal Cell Carcinoma 53 0.035
887
ALC009 Alcoholic Liver Cirrhosis 53 0.035
888
CLR109 Colorectal Adenocarcinoma 51 0.035
889
PST021 Postpartum Depression 50 0.035
890
P FRN006 Frontotemporal Dementia 68 0.035
891
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.035
892
SDD001 Sudden Infant Death Syndrome 61 0.035
893
GRD007 Grade Iii Astrocytoma 59 0.035
894
c CHL119 Cholangitis, Primary Sclerosing 57 0.035
895
JPN002 Japanese Encephalitis 57 0.035
896
LST001 Listeriosis 56 0.035
897
ESP002 Esophageal Varix 51 0.035
898
P SCL009 Sclerosing Cholangitis 48 0.035
899
ANG020 Angiosarcoma 64 0.035
900
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.035
901
TBR011 Tuberculous Meningitis 48 0.035
902
MST019 Mastoiditis 43 0.035
903
GRM010 Germ Cells Tumors 34 0.035
904
NRM005 Neuromuscular Disease 64 0.035
905
MDS022 Mediastinitis 46 0.035
906
CYS009 Cystadenoma 44 0.035
907
c CHR682 Chronic Bilirubin Encephalopathy 39 0.035
908
EXP004 Exophthalmos 52 0.035
909
LNG108 Langerhans Cell Histiocytosis 58 0.035
910
P NJM001 Nijmegen Breakage Syndrome 74 0.035
911
P ESS003 Essential Thrombocythemia 68 0.035
912
BLD131 Bladder Urothelial Carcinoma 62 0.035
913
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.035
914
ALC006 Alcoholic Hepatitis 61 0.035
915
DBT010 Diabetic Neuropathy 54 0.035
916
P ACT008 Actinic Keratosis 53 0.035
917
ADN001 Adenosine Deaminase Deficiency 47 0.035
918
AML001 Amelanotic Melanoma 39 0.035
919
NWB001 Newborn Respiratory Distress Syndrome 58 0.034
920
HPT046 Hepatic Veno-Occlusive Disease 56 0.034
921
HPR003 Heparin-Induced Thrombocytopenia 48 0.034
922
NWC001 Newcastle Disease 45 0.034
923
LPT001 Leptospirosis 66 0.034
924
NRF007 Neurofibroma 64 0.034
925
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.034
926
SBC001 Subacute Sclerosing Panencephalitis 56 0.034
927
MYL001 Myelitis 51 0.034
928
RGH001 Right Bundle Branch Block 48 0.034
929
P MJR007 Major Affective Disorder 1 43 0.034
930
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.034
931
P PLY041 Polymyositis 57 0.034
932
EXS001 Exostosis 46 0.034
933
P GCH001 Gaucher's Disease 63 0.034
934
P SHR029 Short Syndrome 63 0.034
935
CRC006 Carcinoid Syndrome 55 0.034
936
GNG003 Gingival Recession 44 0.034
937
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.034
938
P CRB088 Cerebral Atrophy 37 0.034
939
WST001 West Syndrome 61 0.034
940
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.034
941
BLL006 Bullous Pemphigoid 62 0.034
942
LYM027 Lymphopenia 58 0.034
943
CHK001 Chikungunya 57 0.034
944
TCK001 Tick-Borne Encephalitis 56 0.034
945
P PTT006 Pituitary Adenoma 55 0.034
946
FBR009 Fibrous Dysplasia 48 0.034
947
c DRR009 Diarrhea 6 46 0.034
948
HRN029 Hearing Loss, Noise-Induced 37 0.034
949
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.034
950
HRP008 Herpes Simiae 25 0.034
951
P LNG028 Long Qt Syndrome 66 0.034
952
P AGM001 Agammaglobulinemia 65 0.034
953
PPL049 Papillon-Lefevre Syndrome 65 0.034
954
MSC007 Muscle Hypertrophy 64 0.034
955
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.034
956
DFF036 Differentiated Thyroid Carcinoma 52 0.034
957
SCH012 Schizoaffective Disorder 50 0.034
958
P OPT006 Optic Nerve Disease 60 0.033
959
P PSD015 Pseudohypoparathyroidism 56 0.033
960
NTR046 Neutrophil Migration 50 0.033
961
P MYT002 Myotonic Dystrophy 49 0.033
962
EPC002 Epicondylitis 41 0.033
963
ADR004 Adrenal Cortical Adenocarcinoma 39 0.033
964
PRM329 Premature Aging 35 0.033
965
BHC003 Behcet Syndrome 71 0.033
966
MCC012 Mccune-Albright Syndrome 70 0.033
967
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 56 0.033
968
INT078 Intracranial Thrombosis 49 0.033
969
P CHR071 Charcot-Marie-Tooth Disease 65 0.033
970
P CHR285 Chronic Myelomonocytic Leukemia 60 0.033
971
CND002 Conduct Disorder 51 0.033
972
MTR010 Mature Teratoma 44 0.033
973
TRP009 Triple X Syndrome 42 0.033
974
GST020 Gastric Antral Vascular Ectasia 41 0.033
975
P DYS005 Dyslexia 40 0.033
976
CLF004 Cleft Lip/palate 54 0.033
977
ECT026 Ectopic Pregnancy 50 0.033
978
c DPH024 Diaphragmatic Hernia, Congenital 63 0.033
979
P ACR001 Aicardi-Goutieres Syndrome 62 0.033
980
ANG005 Anogenital Venereal Wart 55 0.033
981
c TBR025 Tuberous Sclerosis 1 77 0.032
982
P CHR012 Chronic Granulomatous Disease 67 0.032
983
P MLG056 Malignant Hyperthermia 67 0.032
984
c FML021 Familial Hypercholesterolemia 66 0.032
985
MRK001 Merkel Cell Carcinoma 65 0.032
986
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.032
987
P LYM033 Lymphoproliferative Syndrome 59 0.032
988
PLL012 Pollen Allergy 46 0.032
989
CRB079 Cerebrospinal Fluid Leak 35 0.032
990
BRN028 Brain Cancer 74 0.032
991
LNG039 Lung Squamous Cell Carcinoma 66 0.032
992
APN008 Apnea, Obstructive Sleep 64 0.032
993
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.032
994
P TCD001 Tic Disorder 53 0.032
995
P LCT001 Lactic Acidosis 51 0.032
996
CYS014 Cystadenocarcinoma 51 0.032
997
CRV040 Cervix Carcinoma 51 0.032
998
RTC005 Reticulosarcoma 47 0.032
999
c GCH015 Gaucher Disease, Type I 70 0.032
1000
PCK003 Pick Disease of Brain 68 0.032
1001
BLM001 Bloom Syndrome 67 0.032
1002
CRP001 Carpal Tunnel Syndrome 67 0.032
1003
ALV005 Alveolar Soft Part Sarcoma 61 0.032
1004
EXT034 Extrinsic Allergic Alveolitis 58 0.032
1005
c PSR023 Psoriasis 1 52 0.032
1006
P OBS001 Obstructive Jaundice 50 0.032
1007
MTC005 Mitochondrial Metabolism Disease 49 0.032
1008
P CTN015 Cutaneous T Cell Lymphoma 49 0.032
1009
IGG001 Iga Glomerulonephritis 48 0.032
1010
CLF056 Cleft Lip with or Without Cleft Palate 47 0.032
1011
P CLL015 Collagen Disease 47 0.032
1012
URT010 Ureteral Obstruction 45 0.032
1013
FCT007 Factor Vii Deficiency 67 0.032
1014
MXD005 Mixed Connective Tissue Disease 58 0.032
1015
CHR100 Chronic Ulcer of Skin 55 0.032
1016
HLL004 Hellp Syndrome 54 0.032
1017
P INT068 Intestinal Disease 53 0.032
1018
STT041 Stuttering 52 0.032
1019
CCN002 Cocaine Abuse 49 0.032
1020
PLC007 Placental Abruption 48 0.032
1021
EPD015 Epidemic Typhus 45 0.032
1022
CND006 Candida Glabrata 32 0.032
1023
PNM001 Pneumocystosis 59 0.032
1024
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.032
1025
BRT054 Brittle Bone Disorder 72 0.032
1026
ADN011 Adenoid Cystic Carcinoma 70 0.032
1027
P DRM010 Dermatomyositis 61 0.032
1028
c LPM012 Lipomatosis, Multiple 60 0.032
1029
PYD001 Pyoderma Gangrenosum 54 0.032
1030
HMP001 Hemopericardium 48 0.032
1031
CRT072 Creutzfeldt-Jakob Disease 70 0.032
1032
P USH001 Usher Syndrome 60 0.032
1033
P SPN052 Spondyloarthropathy 54 0.032
1034
MRG003 Marginal Zone B-Cell Lymphoma 52 0.032
1035
SPS003 Spastic Diplegia 51 0.032
1036
ANR004 Anuria 46 0.032
1037
MLD001 Melioidosis 68 0.031
1038
HYP020 Hyperprolactinemia 64 0.031
1039
PTN001 Patent Foramen Ovale 60 0.031
1040
MCR013 Microphthalmia 57 0.031
1041
P PNM006 Pneumoconiosis 56 0.031
1042
AMB001 Amebiasis 55 0.031
1043
PLV003 Pelvic Inflammatory Disease 55 0.031
1044
HRY003 Hairy Cell Leukemia 55 0.031
1045
ACH005 Achalasia 51 0.031
1046
ASP003 Aseptic Meningitis 51 0.031
1047
P ESN008 Eosinophilic Pneumonia 50 0.031
1048
AMB002 Amblyopia 49 0.031
1049
ANT018 Anthracosis 48 0.031
1050
ACT003 Acute Kidney Tubular Necrosis 45 0.031
1051
CRN322 Coronavirus Infectious Disease 40 0.031
1052
HPR006 Heparin Cofactor Ii Deficiency 40 0.031
1053
SPP007 Suppression Amblyopia 39 0.031
1055
LYM007 Lymphangioleiomyomatosis 69 0.031
1056
PLM070 Pulmonic Stenosis 57 0.031
1057
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.031
1058
CHR177 Chromophobe Renal Cell Carcinoma 57 0.031
1059
GST050 Gastrointestinal System Disease 56 0.031
1060
FCL014 Focal Epilepsy 54 0.031
1061
BCT002 Bacterial Vaginosis 53 0.031
1062
c PRM108 Primary Progressive Multiple Sclerosis 51 0.031
1063
PLR008 Pleurisy 50 0.031
1064
BLR001 Biliary Atresia 50 0.031
1065
URT001 Urethritis 49 0.031
1066
RNL077 Renal Fibrosis 47 0.031
1067
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.031
1068
RDN001 Reading Disorder 40 0.031
1069
GST019 Gastrointestinal Stromal Tumor 78 0.030
1070
P TYS001 Tay-Sachs Disease 69 0.030
1071
PNM010 Pneumothorax, Primary Spontaneous 60 0.030
1072
P LKD001 Leukodystrophy 59 0.030
1073
CRY005 Cryptococcosis 58 0.030
1074
HDR002 Hidradenitis Suppurativa 55 0.030
1075
MYL020 Myelomeningocele 51 0.030
1076
HDR003 Hidradenitis 49 0.030
1077
ANG018 Angiomyolipoma 46 0.030
1078
PLM005 Pleomorphic Lipoma 40 0.030
1079
RTR011 Retroperitoneal Fibrosis 40 0.030
1080
HRL003 Hurler Syndrome 65 0.030
1081
SPP011 Suppression of Tumorigenicity 12 59 0.030
1082
CLC001 Calciphylaxis 51 0.030
1083
STR008 Strongyloidiasis 51 0.030
1084
P BCT020 Bacteremia 2