Search results for 15(S)-HETE

2177 hits were found for 15(S)-HETE

# Family MCID Name MIFTS Score
1
PRT014 Protein S Deficiency 44 0.246
2
c HPT016 Hepatitis B 59 0.168
3
c THR092 Thrombophilia Due to Thrombin Defect 73 0.167
4
SCH014 Schistosomiasis 57 0.164
5
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.163
6
HLX001 Helix Syndrome 47 0.161
7
P LKM002 Leukemia 68 0.160
8
LYM133 Lymphoma, Hodgkin, Classic 69 0.159
9
47X002 47,xyy 49 0.156
10
P DRR001 Diarrhea 55 0.155
11
P MYL006 Myeloid Leukemia 60 0.155
12
P LVR013 Liver Disease 68 0.152
13
P BLD134 Bladder Cancer 79 0.152
14
P NRB001 Neuroblastoma 72 0.150
15
P THL005 Thalassemia 60 0.150
16
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.149
17
P LYM118 Lymphoma 68 0.147
18
DPR016 Depression 63 0.144
19
P ALZ034 Alzheimer Disease 88 0.143
20
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.141
21
CHR178 Chromosomal Triplication 35 0.140
22
P ADN016 Adenocarcinoma 64 0.140
23
ACT119 Acute Promyelocytic Leukemia 63 0.140
24
BRK010 Burkitt Lymphoma 67 0.137
25
MNT002 Mental Depression 58 0.135
26
c LKM061 Leukemia, Acute Myeloid 84 0.132
27
P HPT023 Hepatocellular Carcinoma 100 0.131
28
P OVR042 Ovarian Cancer 88 0.130
29
P TRN020 Turner Syndrome 67 0.129
30
ATM095 Autoimmune Disease 62 0.129
31
CRH001 Crohn's Disease 74 0.128
32
P SCK005 Sickle Cell Disease 50 0.127
33
THR024 Thrombosis 57 0.127
34
DWN001 Down Syndrome 70 0.126
35
P UVT001 Uveitis 57 0.126
36
P LKM062 Leukemia, Acute Lymphoblastic 69 0.125
37
EWN003 Ewing Sarcoma 69 0.125
38
P HRP006 Herpes Simplex 65 0.123
39
P RTN024 Retinoblastoma 73 0.123
40
HMN044 Human Immunodeficiency Virus Type 1 71 0.121
41
c FML008 Familial Retinoblastoma 53 0.120
42
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.120
43
HRW001 Hair Whorl 36 0.120
44
SCK003 Sickle Cell Anemia 74 0.120
45
ADL002 Adult Syndrome 70 0.118
46
P MJR001 Major Depressive Disorder 68 0.118
47
P GST053 Gastric Cancer 83 0.117
48
P ATX030 Ataxia-Telangiectasia 82 0.116
49
TLN003 Telangiectasis 52 0.116
50
PNG002 Pain Agnosia 51 0.115
51
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.115
52
ISC004 Ischemia 58 0.115
53
c SVR001 Severe Acute Respiratory Syndrome 62 0.114
54
DNT012 Dental Caries 53 0.114
55
ALL026 Allergic Hypersensitivity Disease 62 0.114
56
P END033 Endocarditis 57 0.114
57
P PRD006 Prader-Willi Syndrome 59 0.113
58
P KDN018 Kidney Disease 72 0.113
59
P THR015 Thrombophilia 51 0.112
60
P VSC007 Vascular Disease 63 0.111
61
P NTR004 Neutropenia 63 0.108
62
TYP007 Typhoid Fever 63 0.108
63
BRR014 Barrett Esophagus 65 0.108
64
OST012 Osteoarthritis 78 0.108
65
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.107
66
P HPT021 Hepatitis 67 0.107
67
CRB039 Cerebrovascular Disease 67 0.107
68
DFC004 Deficiency Anemia 70 0.106
69
GLL048 Glial Tumor 45 0.106
70
SPN035 Spindle Cell Sarcoma 53 0.106
71
P GLM045 Glioma 63 0.106
72
P CTR002 Cataract 60 0.105
73
P PRK057 Parkinson Disease, Late-Onset 78 0.105
74
CHL014 Cholera 59 0.105
75
c SYS001 Systemic Lupus Erythematosus 86 0.105
76
SQM006 Squamous Cell Carcinoma 60 0.105
77
P DBT009 Diabetes Mellitus 64 0.104
78
MLR004 Malaria 81 0.104
79
LPP008 Lipoprotein Quantitative Trait Locus 62 0.104
80
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.103
81
P ANG001 Angelman Syndrome 69 0.103
82
MYL069 Myeloma, Multiple 85 0.102
83
SRC014 Sarcoma 65 0.102
84
c PRC016 Pre-Eclampsia 63 0.101
85
PLM033 Pulmonary Embolism 59 0.101
86
TXC005 Toxic Shock Syndrome 62 0.101
87
c PNS012 Paine Syndrome 61 0.100
88
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.100
89
PRP030 Purpura 54 0.100
90
c SML038 Small Cell Cancer of the Lung 65 0.100
91
HMP009 Haemophilus Influenzae 43 0.099
92
HMG005 Hemoglobinopathy 56 0.099
93
THY029 Thyroid Carcinoma 59 0.099
94
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.098
95
CHL068 Cholestasis 61 0.098
96
CHC001 Chickenpox 60 0.098
97
PRT036 Peritonitis 64 0.098
98
AST005 Asthma 76 0.098
99
P NRP001 Neuropathy 56 0.097
100
P SZR006 Seizure Disorder 56 0.097
101
STR067 Stroke, Ischemic 81 0.097
102
P INF032 Infertility 57 0.097
103
GLB015 Glioblastoma Multiforme 75 0.096
104
P CHR345 Chronic Pain 44 0.096
105
OST159 Osteogenic Sarcoma 66 0.096
106
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.096
107
c BTT014 Beta-Thalassemia 74 0.096
108
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.095
109
P BCL017 B-Cell Lymphoma 58 0.095
110
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.095
111
CRV035 Cervical Cancer 76 0.095
112
ALC007 Alcohol Dependence 66 0.094
113
ULC004 Ulcerative Colitis 73 0.094
114
GST045 Gastroenteritis 59 0.094
115
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.094
116
P CRN300 Coronary Heart Disease 1 63 0.094
117
CYS001 Cystic Fibrosis 81 0.094
118
P TRM003 Tremor 54 0.093
119
P LPS004 Lupus Erythematosus 61 0.092
120
P VSC011 Vasculitis 62 0.092
121
CYT002 Cytokine Deficiency 42 0.092
122
P MNN013 Meningitis 66 0.092
123
P THR014 Thrombocytopenia 67 0.091
124
PST011 Pustulosis of Palm and Sole 52 0.091
125
ANX010 Anxiety 73 0.091
126
IMM167 Immune Deficiency Disease 78 0.091
127
ATX019 Ataxia with Vitamin E Deficiency 42 0.091
128
P RHM011 Rheumatoid Arthritis 80 0.091
129
ENH001 Enhanced S-Cone Syndrome 57 0.090
130
P PNM007 Pneumonia 68 0.090
131
P SCL018 Scoliosis 60 0.089
132
P SLM003 Salmonellosis 55 0.089
133
VSL002 Visual Epilepsy 59 0.089
134
P INF038 Influenza 68 0.089
135
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.089
136
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.089
137
END086 End Stage Renal Disease 51 0.089
138
MSL001 Measles 62 0.088
139
ART140 Arteries, Anomalies of 52 0.088
140
TTN003 Tetanus 65 0.088
141
RTN023 Retinitis 46 0.087
142
NRR001 Neuroretinitis 42 0.087
143
MYL009 Myelodysplastic Syndrome 70 0.086
144
HYP056 Hypoglycemia 66 0.086
145
c HPT073 Hepatitis C Virus 72 0.086
146
c RHB024 Rhabdomyosarcoma 2 67 0.086
147
P PLM037 Pulmonary Hypertension 67 0.086
148
c HPT003 Hepatitis a 62 0.086
149
P CRD119 Cardiac Arrest 67 0.086
150
DPH001 Diphtheria 60 0.085
151
HMC014 Homocysteinemia 53 0.085
152
BCT022 Bacterial Infectious Disease 56 0.085
153
END040 Endogenous Depression 55 0.085
154
SVR004 Severe Combined Immunodeficiency 73 0.085
155
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.085
156
P HYP265 Hypotonia 43 0.085
157
HNS001 Hansen's Disease 34 0.085
158
CVD001 Covid-19 44 0.085
159
P DMN002 Dementia 66 0.084
160
P EXN002 Exanthem 57 0.084
161
c PRM038 Primary Agammaglobulinemia 44 0.084
162
P HYP086 Hypothyroidism 69 0.084
163
DSS009 Disseminated Intravascular Coagulation 57 0.084
164
c CHR684 Chronic Kidney Disease 70 0.084
165
P LPR021 Leprosy 3 69 0.083
166
HYP066 Hyperglycemia 61 0.083
167
P TRC086 Trichohepatoenteric Syndrome 1 62 0.082
168
LYM019 Lymphosarcoma 46 0.082
169
c SPN225 Spondyloarthropathy 1 73 0.082
170
ANR007 Anorexia Nervosa 63 0.082
171
ACQ007 Acquired Immunodeficiency Syndrome 60 0.082
172
NRT001 Neurotic Disorder 53 0.082
173
FTT001 Fatty Liver Disease 61 0.082
174
c ACT073 Acute Leukemia 58 0.081
175
ANR040 Aneurysm 59 0.081
176
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.081
177
ESP021 Esophageal Cancer 90 0.081
178
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.081
179
CLT003 Colitis 62 0.081
180
PRS045 Prostatic Hypertrophy 53 0.081
181
P ENC018 Encephalopathy 61 0.081
182
P NPH012 Nephrotic Syndrome 60 0.080
183
MST005 Mastitis 53 0.080
184
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.079
185
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.079
186
c ACT075 Acute Myocardial Infarction 57 0.079
187
P ATS364 Autism 70 0.079
188
P ENC004 Encephalitis 61 0.079
189
SPL018 Splenomegaly 48 0.079
190
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.079
191
P ALC033 Alcohol Use Disorder 58 0.079
192
P RSP003 Respiratory Failure 74 0.079
193
c HYP836 Hypercholesterolemia, Familial, 1 73 0.079
194
P LTR001 Lateral Sclerosis 54 0.078
195
P HYP098 Hypereosinophilic Syndrome 67 0.078
196
ANG054 Angina Pectoris 66 0.078
197
P RBL001 Rubella 59 0.078
198
P MCR010 Microcephaly 59 0.078
199
OTT002 Otitis Media 72 0.078
200
P DRM053 Dermatitis, Atopic 66 0.078
201
P EPL164 Epilepsy 71 0.078
202
P SKN015 Skin Carcinoma 66 0.077
203
P HDC001 Headache 57 0.077
204
P HRS035 Hirschsprung Disease 1 65 0.077
205
PRS021 Prostatic Adenoma 51 0.076
206
P PHC003 Pheochromocytoma 71 0.076
207
GST092 Gastroesophageal Reflux 67 0.076
208
INF034 Infective Endocarditis 53 0.076
209
PRT011 Protein C Deficiency 44 0.076
210
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.076
211
PLM001 Pulmonary Tuberculosis 69 0.076
212
P LKM071 Leukemia, Chronic Lymphocytic 79 0.075
213
P END044 Endometriosis 63 0.075
214
PLS011 Plasmacytoma 56 0.075
215
P RNG032 Ring Chromosome 42 0.075
216
BCK006 Back Pain 42 0.075
217
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.075
218
P RTN008 Retinitis Pigmentosa 79 0.075
219
P MYP004 Myopathy 70 0.075
220
P MLT020 Multiple Sclerosis 72 0.075
221
RSC001 Rosacea 54 0.075
222
VLV047 Volvulus of Midgut 49 0.074
223
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.074
224
P ANR048 Aniridia 1 63 0.074
225
THR013 Thoracic Outlet Syndrome 54 0.074
226
FBR047 Fibromyalgia 58 0.074
227
P SYP003 Syphilis 58 0.074
228
c MGR028 Migraine with or Without Aura 1 67 0.074
229
P PRD008 Periodontitis 64 0.074
230
LSH001 Leishmaniasis 63 0.073
231
P KLZ004 Kala-Azar 1 41 0.073
232
IRN002 Iron Metabolism Disease 57 0.073
233
OST017 Osteomyelitis 64 0.073
234
TRN018 Transitional Cell Carcinoma 56 0.073
235
LPD008 Lipid Metabolism Disorder 62 0.073
236
IMP005 Impotence 52 0.073
237
ADR040 Adrenal Gland Pheochromocytoma 46 0.073
238
ORL011 Oral Cancer 60 0.073
239
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.073
240
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.073
241
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.073
242
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.073
243
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.073
244
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.073
245
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.073
246
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.073
247
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.073
248
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.073
249
c HPT001 Hepatitis C 62 0.073
250
P AST007 Astrocytoma 51 0.073
251
PLM031 Poliomyelitis 64 0.073
252
P ECL001 Eclampsia 50 0.073
253
ACN002 Acanthosis Nigricans 60 0.073
254
c ATR087 Atrial Standstill 1 75 0.073
255
PRS129 Prostatic Hyperplasia, Benign 49 0.073
256
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.072
257
OCL069 Ocular Motor Apraxia 51 0.072
258
DYS073 Dysphagia 50 0.072
259
HRT011 Heart Septal Defect 50 0.072
260
BRR002 Barrett's Adenocarcinoma 36 0.072
261
STM007 Stomatitis 50 0.072
262
END057 Endometrial Cancer 74 0.072
263
NTR005 Nutritional Deficiency Disease 62 0.072
264
AGN016 Aging 56 0.072
266
P HNT016 Huntington Disease 72 0.072
267
c BRN108 Branchiootic Syndrome 1 62 0.071
268
PPT005 Peptic Ulcer Disease 59 0.071
270
ATX010 Ataxia Neuropathy Spectrum 34 0.071
271
ACT064 Acute Necrotizing Encephalitis 33 0.071
272
BLD137 Blood Group--Ahonen 16 0.071
273
c BSL007 Basal Cell Carcinoma 68 0.071
274
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.071
275
P SRC025 Sarcoidosis 1 70 0.071
276
P BPL003 Bipolar Disorder 56 0.070
277
P RTN016 Retinal Degeneration 53 0.070
278
c MCR113 Microvascular Complications of Diabetes 3 52 0.070
279
c ACT068 Acute Cystitis 63 0.070
280
P FBR017 Fibrosarcoma 56 0.070
281
c ALP101 Alpha-Thalassemia 62 0.070
282
P MCR115 Microvascular Complications of Diabetes 5 66 0.069
283
P SCH015 Schizophrenia 74 0.069
284
DSS008 Disease of Mental Health 58 0.069
285
c MJR024 Major Affective Disorder 9 41 0.069
286
c MJR022 Major Affective Disorder 8 38 0.069
287
c ACT027 Acute Pancreatitis 60 0.068
288
CHL079 Children's Interstitial Lung Disease 26 0.068
289
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.068
290
c LKM005 Leukemia, T-Cell, Chronic 34 0.068
291
P LNG064 Lung Cancer Susceptibility 3 78 0.068
292
PPL052 Papillomatosis, Confluent and Reticulated 33 0.068
293
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.068
294
P PLM036 Pulmonary Fibrosis 65 0.068
295
c MCR120 Microvascular Complications of Diabetes 7 47 0.068
296
c MCR130 Microvascular Complications of Diabetes 6 41 0.068
297
c MCR133 Microvascular Complications of Diabetes 4 41 0.068
298
c FNC043 Fanconi Anemia, Complementation Group E 62 0.068
300
P THY032 Thyroiditis 52 0.067
301
P MSC005 Muscular Dystrophy 66 0.067
302
P HMP007 Hemophilia 51 0.067
303
P RHN004 Rhinitis 57 0.067
304
KPS004 Kaposi Sarcoma 75 0.067
305
P APL001 Aplastic Anemia 74 0.067
306
PPL022 Papilloma 54 0.066
307
P NSP012 Nasopharyngeal Carcinoma 66 0.066
308
RHM001 Rheumatic Fever 60 0.066
309
c DLT002 Dilated Cardiomyopathy 79 0.066
310
CRD132 Cardiac Conduction Defect 58 0.066
311
P HYP076 Hyperthyroidism 55 0.066
312
c ATS007 Autism Spectrum Disorder 67 0.066
313
P ATR011 Atrial Fibrillation 66 0.066
314
P PRS038 Personality Disorder 65 0.066
315
ADP007 Adie Pupil 39 0.065
316
P OVR082 Overgrowth Syndrome 50 0.065
317
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.065
318
BNR002 Bone Resorption Disease 48 0.065
319
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.065
320
GST023 Gastric Ulcer 53 0.065
321
P GRF003 Graft-Versus-Host Disease 72 0.065
322
SPN186 Spinal Cord Injury 60 0.065
323
c ACT071 Acute Kidney Failure 60 0.065
324
P HYP061 Hypertrophic Cardiomyopathy 70 0.065
325
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.065
326
P HYP069 Hyperparathyroidism 63 0.065
327
P PLY019 Polyneuropathy 56 0.065
328
DFF005 Diffuse Large B-Cell Lymphoma 55 0.064
329
P OPN001 Open-Angle Glaucoma 49 0.064
330
P GST044 Gastritis 56 0.064
331
P CHL066 Cholangitis 51 0.064
332
PSY004 Psychotic Disorder 67 0.064
333
CHL123 Chlamydia 59 0.064
334
P PRP034 Purpura Fulminans 43 0.064
335
AMN003 Amnestic Disorder 54 0.064
336
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.064
337
DYS015 Dysentery 52 0.064
338
CHL065 Cholangiocarcinoma 68 0.064
339
ORL015 Oral Squamous Cell Carcinoma 43 0.064
340
P KDN017 Kidney Cancer 60 0.064
341
IGR001 Ige Responsiveness, Atopic 59 0.063
342
ATS010 Autosomal Recessive Disease 48 0.063
343
P RHB003 Rhabdomyosarcoma 63 0.063
344
c NRF023 Neurofibromatosis, Type Ii 80 0.063
345
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.063
346
P MMP001 Mumps 58 0.063
347
HRP004 Herpes Zoster 60 0.063
348
CHG001 Chagas Disease 66 0.063
349
SQM002 Squamous Cell Papilloma 46 0.063
350
HNM002 Hinman Syndrome 27 0.063
351
P HYD006 Hydrocephalus 66 0.062
352
P FML011 Familial Adenomatous Polyposis 72 0.062
353
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.062
354
P CNR004 Cone-Rod Dystrophy 2 73 0.062
355
P DYS154 Dystonia 65 0.062
356
APH002 Aphasia 57 0.062
357
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.062
358
P INS002 in Situ Carcinoma 53 0.062
359
CRH005 Crohn's Colitis 53 0.062
360
P PRP019 Peripheral Nervous System Disease 58 0.062
361
HPT082 Hepatic Adenomas, Familial 44 0.062
362
VRC005 Varicose Veins 60 0.062
363
PHR003 Pharyngitis 57 0.062
364
INT079 Intrahepatic Cholangiocarcinoma 51 0.062
365
P HMN010 Hemangioma 61 0.062
366
ONC002 Onchocerciasis 52 0.061
367
TBC004 Tobacco Addiction 64 0.061
368
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.061
369
P MYS005 Myositis 56 0.061
370
P VNT002 Ventricular Septal Defect 60 0.061
371
HDN002 Head Injury 46 0.061
372
P MSC003 Muscular Atrophy 52 0.061
373
P DDN001 Duodenal Ulcer 52 0.061
374
INT007 Intermediate Coronary Syndrome 55 0.061
375
c VRL010 Viral Hepatitis 52 0.061
376
P BNG032 Benign Mesothelioma 46 0.061
377
P ANT006 Antiphospholipid Syndrome 55 0.061
378
OST003 Osteonecrosis 61 0.061
379
P TXP001 Toxoplasmosis 60 0.061
380
CNS004 Constipation 58 0.061
381
INS024 Insulin-Like Growth Factor I 79 0.061
382
KHL003 Kohlschutter-Tonz Syndrome 65 0.061
383
OVR094 Ovarian Epithelial Cancer 38 0.061
384
MDD011 Mood Disorder 62 0.060
385
SFT003 Soft Tissue Sarcoma 56 0.060
386
P AMY004 Amyloidosis 70 0.060
387
INT017 Intestinal Schistosomiasis 48 0.060
388
MDD018 Middle East Respiratory Syndrome 43 0.059
389
SPN051 Spondylitis 51 0.059
390
P MYP006 Myopia 55 0.059
391
AMN001 Amenorrhea 54 0.059
392
HMS001 Hemosiderosis 54 0.059
393
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.059
394
P MLN007 Male Infertility 55 0.059
395
RTN017 Retinal Detachment 61 0.059
396
EYD002 Eye Disease 58 0.059
397
IDP070 Idiopathic Scoliosis 42 0.059
398
CLF027 Cleft Palate, Isolated 64 0.059
399
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.059
400
P TRT010 Teratoma 52 0.058
401
P OST002 Osteoporosis 74 0.058
402
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.058
403
c SCL052 Scleroderma, Familial Progressive 61 0.058
404
INF009 Inflammatory Spondylopathy 31 0.058
405
P SLP006 Sleep Apnea 69 0.058
406
ALL003 Allergic Rhinitis 67 0.058
407
GST040 Gastric Adenocarcinoma 70 0.058
408
ART016 Aortic Aneurysm 69 0.058
409
P AXN002 Axenfeld-Rieger Syndrome 59 0.058
410
P HML002 Hemolytic Anemia 63 0.058
411
P CYS018 Cystitis 59 0.058
412
ANT024 Anthrax Disease 58 0.058
413
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.057
414
PRT013 Portal Hypertension 59 0.057
415
CNN005 Connective Tissue Disease 68 0.057
416
RCK004 Rickets 68 0.057
417
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.057
418
ENT011 Enterocolitis 51 0.057
419
P NRF002 Neurofibromatosis 56 0.057
420
SYN036 Syncope 45 0.057
421
P RRH023 Rare Hereditary Hemochromatosis 41 0.057
422
HYP080 Hypogonadism 50 0.057
423
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.057
424
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.057
425
P PNC044 Pancreatitis 61 0.057
426
ALL006 Allergic Asthma 56 0.057
427
P SPP010 Suppressor of Tumorigenicity 3 51 0.057
428
P CND004 Candidiasis 58 0.056
429
c DBT099 Diabetes Mellitus, Type I 65 0.056
430
c INF071 Inflammatory Bowel Disease 1 67 0.056
431
PLY150 Polykaryocytosis Inducer 31 0.056
432
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.056
433
SMN007 Seminoma 43 0.056
434
AND002 Androgen Insensitivity Syndrome 66 0.056
435
PRT018 Portal Vein Thrombosis 50 0.056
436
WLL004 Wallerian Degeneration 39 0.056
437
P SBS003 Substance Abuse 55 0.055
438
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.055
439
GT001 Gout 64 0.055
440
PNC001 Pancytopenia 54 0.055
441
NNL006 Non-Alcoholic Steatohepatitis 54 0.055
442
INT075 Intracranial Hypertension 53 0.055
443
PRP027 Peripheral Vascular Disease 71 0.055
444
CRB037 Cerebral Palsy 69 0.055
445
c WLM018 Wilms Tumor 5 61 0.055
446
ALL014 Allergic Encephalomyelitis 38 0.055
447
PNM008 Pneumothorax 56 0.055
448
P RCT021 Rectum Cancer 52 0.055
449
P MYS003 Myasthenia Gravis 68 0.055
450
ALR002 Al-Raqad Syndrome 33 0.054
451
PST053 Postherpetic Neuralgia 40 0.054
452
ETN001 Eating Disorder 60 0.054
453
PTH003 Pathologic Nystagmus 52 0.054
454
P MDL005 Medulloblastoma 77 0.054
455
ENT004 Enthesopathy 49 0.054
456
P ASP006 Aspergillosis 69 0.054
457
P ART023 Arthropathy 62 0.054
458
P BRN022 Bronchiectasis 59 0.054
459
TRY001 Trypanosomiasis 50 0.053
460
P NGH001 Night Blindness 48 0.053
461
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.053
462
CYT008 Cytomegalovirus Infection 57 0.053
463
P INT070 Intestinal Obstruction 58 0.053
464
P ALP106 Alport Syndrome 1, X-Linked 55 0.053
465
CLF001 Cleft Lip 53 0.053
466
SPT004 Septic Arthritis 58 0.053
467
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.053
468
HLC007 Helicobacter Pylori Infection 59 0.053
469
KRT019 Keratitis, Hereditary 65 0.053
470
RHM028 Rheumatic Heart Disease 53 0.053
471
c MNN043 Meningioma, Familial 74 0.053
472
ANX004 Anoxia 40 0.053
473
TRN015 Transient Cerebral Ischemia 63 0.053
474
P SML001 Small Cell Carcinoma 52 0.053
475
P MYC008 Myocarditis 59 0.052
476
P TBR001 Tuberous Sclerosis 70 0.052
477
FSC004 Fasciitis 50 0.052
478
CLN015 Colon Adenocarcinoma 65 0.052
479
P LRY044 Larynx Cancer 55 0.052
480
P PRP029 Porphyria 62 0.052
481
PST092 Posttransplant Acute Limbic Encephalitis 29 0.052
482
P TTR001 Tetralogy of Fallot 70 0.052
483
P SYS005 Systemic Scleroderma 68 0.052
484
c FNC027 Fanconi Anemia, Complementation Group a 81 0.052
485
PTT037 Pituitary Tumors 44 0.052
486
LPT014 Leptin Deficiency or Dysfunction 74 0.052
487
GST033 Gestational Diabetes 61 0.052
488
MCS002 Mucositis 56 0.052
489
LWC001 Low Compliance Bladder 43 0.052
490
MNN042 Meningioma, Radiation-Induced 62 0.051
491
SPN021 Spinal Meningioma 50 0.051
492
THR016 Thrombophlebitis 51 0.051
493
ERY003 Erythema Multiforme 58 0.051
494
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.051
495
P ART021 Arteriosclerosis 54 0.051
496
URM002 Uremia 49 0.051
497
P MYC084 Mycobacterium Tuberculosis 1 68 0.051
498
P END047 Endophthalmitis 53 0.051
499
P URT039 Urticaria 58 0.051
500
c ACT134 Acute Liver Failure 56 0.051
501
P PTS002 Ptosis 53 0.051
502
c GLC092 Glaucoma, Primary Open Angle 62 0.051
503
P PRM006 Primary Biliary Cirrhosis 62 0.051
504
P PLY018 Polycythemia 56 0.051
505
GLC003 Glucose Intolerance 54 0.051
506
CLL003 Cellulitis 54 0.051
507
PPT001 Peptic Esophagitis 52 0.051
508
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.051
509
HYD002 Hydronephrosis 60 0.051
510
P GLL022 Guillain-Barre Syndrome 59 0.051
511
c DWL002 Dowling-Degos Disease 1 58 0.051
512
KRT009 Keratosis 51 0.050
513
INT066 Interstitial Lung Disease 60 0.050
514
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.050
515
SCR001 Secretory Meningioma 41 0.050
516
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
517
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.050
518
LYM017 Lyme Disease 64 0.050
519
P MVM001 Movement Disease 63 0.050
520
P RTN018 Retinal Disease 53 0.050
521
P SCL057 Scoliosis, Isolated 1 41 0.050
522
c EXD008 Exudative Vitreoretinopathy 1 71 0.050
523
ECH003 Echinococcosis 53 0.050
524
SVR097 Severe Cutaneous Adverse Reaction 69 0.050
525
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.050
526
PRP016 Paraplegia 52 0.050
527
FLR002 Filariasis 55 0.050
528
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.050
529
c GLL024 Gallbladder Disease 1 53 0.050
530
P FRD001 Friedreich Ataxia 64 0.049
531
NRL016 Neural Tube Defects 82 0.049
532
GTR002 Goiter 53 0.049
533
SKN019 Skin Melanoma 68 0.049
534
P STR020 Strabismus 55 0.049
535
MCH006 Mechanical Strabismus 42 0.049
536
CRN030 Coronary Stenosis 50 0.049
537
SBC016 Subacute Delirium 44 0.049
538
P HYP750 Hypertriglyceridemia, Familial 62 0.049
539
c PST005 Posterior Uveitis 54 0.049
540
HRL004 Hurler-Scheie Syndrome 55 0.049
541
MYF002 Myofascial Pain Syndrome 42 0.049
542
P ALP008 Alopecia 54 0.049
543
RYN005 Raynaud Phenomenon 47 0.049
544
P CLC063 Celiac Disease 1 66 0.048
545
PLS009 Plasma Cell Neoplasm 51 0.048
546
P PLY011 Polycystic Ovary Syndrome 56 0.048
547
WST005 West Nile Virus 54 0.048
548
CHL004 Cholelithiasis 49 0.048
549
c ACT135 Acute Graft Versus Host Disease 52 0.048
550
ERY066 Erythema Multiforme Major 30 0.048
551
BRC012 Brucellosis 64 0.048
552
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.048
553
HPT022 Hepatoblastoma 56 0.048
554
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.048
555
LYM040 Lymphoblastic Lymphoma 54 0.048
556
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.048
557
PLG002 Plague 63 0.048
558
P PLY014 Polycystic Kidney Disease 62 0.048
559
P LMY004 Leiomyosarcoma 63 0.048
560
PSR001 Psoriatic Arthritis 61 0.048
561
P ADL017 Adult T-Cell Leukemia 56 0.048
562
SCH036 Scheie Syndrome 72 0.047
563
P HMC002 Homocystinuria 53 0.047
564
P CNJ013 Conjunctivitis 65 0.047
565
ILS001 Ileus 51 0.047
566
PHN003 Phenylketonuria 75 0.047
567
APP008 Appendicitis 61 0.047
568
DBL002 Double Outlet Right Ventricle 56 0.047
569
ACT084 Acute Stress Disorder 47 0.047
570
KRT013 Keratolytic Winter Erythema 46 0.047
571
P BND020 Bone Disease 59 0.047
572
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.047
573
ALB002 Albinism 46 0.047
574
P AVS003 Avascular Necrosis 42 0.047
575
c ATM011 Autoimmune Hepatitis 63 0.047
576
P PNC025 Panic Disorder 53 0.047
577
P THY023 Thymoma 65 0.047
578
CHL067 Cholecystitis 57 0.047
579
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.047
580
P GRV001 Graves' Disease 55 0.047
581
HRT012 Heart Valve Disease 53 0.047
582
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.047
583
ING001 Inguinal Hernia 60 0.047
584
PLM010 Pulmonary Edema 54 0.047
585
P GLL018 Gallbladder Cancer 57 0.047
586
CTN007 Cutaneous Leishmaniasis 62 0.047
587
P MTR003 Mitral Valve Stenosis 50 0.047
588
ART001 Arterial Tortuosity Syndrome 66 0.047
589
NSS002 Neisseria Meningitidis Infection 47 0.047
590
P DBT005 Diabetes Insipidus 55 0.047
591
P FLL037 Follicular Lymphoma 67 0.046
592
c MLG084 Malignant Fibrous Histiocytoma 63 0.046
593
NND010 Nondisjunction 34 0.046
594
PLS007 Plasmodium Falciparum Malaria 52 0.046
595
AZS001 Azoospermia 50 0.046
596
KWS002 Kawasaki Disease 65 0.046
597
CLR108 Colorectal Adenoma 64 0.046
598
PST028 Post-Traumatic Stress Disorder 58 0.046
599
HYP005 Hypokalemia 55 0.046
600
NRT004 Neuritis 52 0.046
601
P MMB011 Membranous Nephropathy 50 0.046
602
GNG013 Gingivitis 59 0.046
603
RBS001 Rabies 58 0.046
604
MCL006 Macular Retinal Edema 55 0.046
605
IRD001 Iridocyclitis 53 0.046
606
YLL002 Yellow Fever 61 0.046
607
HND015 Hand Skill, Relative 33 0.046
608
P DNG005 Dengue Virus 59 0.046
609
c THY107 Thymoma, Familial 52 0.046
610
LMY002 Leiomyoma 52 0.046
611
49X006 49, Xxxxy Syndrome 41 0.046
612
SHG001 Shigellosis 60 0.046
613
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.046
614
P SLP005 Sleep Disorder 59 0.046
615
P SNS001 Sensorineural Hearing Loss 60 0.046
616
P PYL005 Pyelonephritis 56 0.046
617
PRC013 Pericarditis 54 0.046
618
c HMP029 Hemophilia a 67 0.045
619
CCC001 Coccidioidomycosis 58 0.045
620
SYN007 Synovitis 54 0.045
621
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.045
622
PLC002 Plica Syndrome 36 0.045
623
HYP748 Hypertelorism 50 0.045
624
OBS002 Obsessive-Compulsive Disorder 68 0.045
625
P NRV007 Nervous System Disease 66 0.045
626
P ANP001 Anaplastic Large Cell Lymphoma 58 0.045
627
P GND004 Gonadal Dysgenesis 48 0.045
628
VSC002 Vascular Dementia 57 0.045
629
SLP001 Sleeping Sickness 54 0.045
630
PFF001 Pfeiffer Syndrome 79 0.045
631
PLY001 Polycythemia Vera 69 0.045
632
CRD137 Cardiogenic Shock 47 0.045
633
BLR008 Bilirubin Metabolic Disorder 57 0.045
634
FDL002 Food Allergy 51 0.045
635
VTM033 Vitamin K Deficiency Bleeding 48 0.045
636
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.045
637
SCB001 Scabies 50 0.045
638
TST014 Testicular Cancer 46 0.045
639
P CRN037 Craniosynostosis 68 0.044
640
INS001 Insulinoma 60 0.044
641
MNN009 Meningoencephalitis 49 0.044
642
ART002 Arts Syndrome 64 0.044
643
BRN056 Bronchopulmonary Dysplasia 57 0.044
644
GRN017 Granulocytopenia 44 0.044
645
c FML001 Familial Atrial Fibrillation 65 0.044
646
P ART005 Arteriovenous Malformation 65 0.044
647
CHR074 Choriocarcinoma 47 0.044
648
RFR003 Refractive Error 43 0.044
649
c FML035 Familial Hyperlipidemia 55 0.044
650
ART074 Aortic Dissection 52 0.044
651
c HMP004 Hemophilia B 68 0.044
652
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.044
653
HST010 Histiocytosis 48 0.044
654
PRN019 Perinatal Necrotizing Enterocolitis 59 0.044
655
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.044
656
ATR057 Atrioventricular Block 55 0.044
657
PLC008 Placenta Disease 50 0.043
658
AST006 Astigmatism 47 0.043
659
KRT002 Keratomalacia 47 0.043
660
FCL012 Facial Paralysis 46 0.043
661
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.043
662
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.043
663
VRL011 Viral Infectious Disease 61 0.043
664
DCT002 Ductal Carcinoma in Situ 59 0.043
665
GST010 Gestational Trophoblastic Neoplasm 46 0.043
666
c CHR064 Chronic Monocytic Leukemia 33 0.043
667
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.043
668
MYL005 Myelofibrosis 70 0.043
669
NRL005 Neurilemmoma 60 0.043
670
ANS003 Anisakiasis 40 0.043
671
P RTN022 Retinal Vein Occlusion 53 0.043
672
VRC001 Varicocele 49 0.043
673
ACR007 Acromegaly 71 0.042
674
HMP005 Hemiplegia 55 0.042
675
HYP014 Hyperuricemia 52 0.042
676
P CHN012 Chondrosarcoma 56 0.042
677
c HMC039 Hemochromatosis, Type 1 74 0.042
678
P OPT009 Optic Neuritis 57 0.042
679
HYP060 Hyperinsulinism 54 0.042
680
P EPD016 Epidermolysis Bullosa 53 0.042
681
P DVL012 Developmental Dysplasia of the Hip 1 38 0.042
682
P ADL010 Adult Respiratory Distress Syndrome 65 0.042
683
BCT004 Bacteriuria 49 0.042
684
c JVN010 Juvenile Rheumatoid Arthritis 64 0.042
685
P MTC069 Mitochondrial Disorders 56 0.042
686
TTR011 Tetraploidy 47 0.042
687
WRN001 Werner Syndrome 69 0.042
688
DCB001 Decubitus Ulcer 61 0.042
689
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.042
690
AVN001 Avian Influenza 59 0.042
691
PLR007 Pleural Empyema 50 0.042
692
SXL003 Sexual Disorder 47 0.042
693
P SPN046 Spinal Muscular Atrophy 62 0.042
694
MRF001 Marfan Syndrome 77 0.042
695
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.042
696
STT001 Status Epilepticus 60 0.041
697
P PMP001 Pemphigus 54 0.041
698
SPN019 Spondylolisthesis 51 0.041
699
NCR007 Necrotizing Fasciitis 48 0.041
700
PYD002 Pyoderma 50 0.041
701
NPH009 Nephrolithiasis 55 0.041
702
PPL002 Papillary Carcinoma 47 0.041
703
SPS057 Spasticity 45 0.041
704
MYC088 Mycobacterium Avium Complex Infections 29 0.041
705
AND005 Androgen Insensitivity Syndrome, Mild 19 0.041
706
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.041
707
c HPT015 Hepatitis D 49 0.041
708
BDD001 Budd-Chiari Syndrome 63 0.041
709
P SJG008 Sjogren Syndrome 61 0.041
710
EMB004 Embryonal Carcinoma 56 0.041
711
PLY100 Polyploidy 40 0.041
712
c OVR114 Ovarian Cancer 1 38 0.041
713
PNC129 Pancreatic Adenocarcinoma 68 0.041
714
P MLN069 Melanoma, Uveal 59 0.041
715
c ART101 Aortic Valve Disease 2 65 0.040
716
c WLM013 Wilms Tumor 1 65 0.040
717
LMB062 Limb Ischemia 55 0.040
718
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.040
719
DMY004 Demyelinating Disease 52 0.040
720
CRV045 Cervical Intraepithelial Neoplasia 39 0.040
721
KRN002 Kearns-Sayre Syndrome 63 0.040
722
CYN002 Cyanosis, Transient Neonatal 45 0.040
723
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.040
724
P PLY006 Polydactyly 59 0.040
725
c PRM005 Primary Hyperparathyroidism 58 0.040
726
FLR001 Filarial Elephantiasis 55 0.040
727
P PLM034 Pulmonary Emphysema 55 0.040
728
KRT006 Keratoconjunctivitis 53 0.040
729
P HYP040 Hypospadias 51 0.040
730
c MLG068 Malignant Glioma 46 0.040
731
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.040
732
c DNG003 Dengue Disease 59 0.040
733
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 28 0.040
734
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.040
735
MTH009 Mouth Disease 56 0.040
736
P MNC007 Monocytic Leukemia 53 0.040
737
RTN001 Retinal Vasculitis 47 0.040
738
BNG077 Benign Idiopathic Neonatal Seizures 26 0.040
739
MSC157 Muscular Dystrophy, Duchenne Type 72 0.040
740
c PRS136 Prostate Cancer, Hereditary, 6 33 0.040
741
c PRS130 Prostate Cancer, Hereditary, 8 32 0.040
742
CRT013 Carotid Stenosis 50 0.039
743
P TMP001 Temporal Lobe Epilepsy 50 0.039
744
FSC002 Fascioliasis 42 0.039
745
c MST023 Mesothelioma, Malignant 57 0.039
746
VSC003 Visceral Leishmaniasis 55 0.039
747
c BCT007 Bacterial Meningitis 55 0.039
748
PRP080 Peripheral Artery Disease 53 0.039
749
THR004 Thrombocytosis 51 0.039
750
HPT004 Hepatic Coma 45 0.039
751
P MTR014 Motor Neuron Disease 65 0.039
752
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.039
753
CYS005 Cysticercosis 53 0.039
754
P PRN023 Prion Disease 57 0.039
755
c HMG029 Hemoglobin Se Disease 39 0.039
756
STN013 Stenotrophomonas Maltophilia Infection 25 0.039
757
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.039
758
THY111 Thyroid Carcinoma, Familial Medullary 67 0.039
759
THY030 Thyroid Gland Disease 52 0.039
760
SPS019 Spastic Paraparesis 38 0.039
761
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.039
762
HSH003 Hashimoto Thyroiditis 62 0.039
763
THY122 Thyroid Gland Cancer 57 0.039
764
TRC023 Trichinosis 53 0.039
765
c SCN007 Secondary Hyperparathyroidism 51 0.039
766
CHR078 Chorioretinitis 50 0.039
767
LPR001 Lepromatous Leprosy 50 0.039
768
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.039
769
SCR015 Scarlet Fever 39 0.039
770
MTY003 Mutyh Polyposis 30 0.039
771
LYM009 Lymphocytic Choriomeningitis 47 0.038
772
LKP003 Leukoplakia 39 0.038
773
P KRT007 Keratoconus 50 0.038
774
P ART018 Aortic Valve Insufficiency 49 0.038
775
CMP010 Complex Regional Pain Syndrome 58 0.038
776
BRN002 Bronchiolitis 59 0.038
777
ANK001 Ankylosis 51 0.038
778
c MTR002 Mitral Valve Insufficiency 48 0.038
779
NRG002 Neurogenic Bladder 55 0.038
780
INT051 Intussusception 53 0.038
781
P PLV020 Pelvic Organ Prolapse 57 0.038
782
P MYM013 Moyamoya Disease 1 57 0.038
783
P HML001 Hemolytic-Uremic Syndrome 53 0.038
784
c INH030 Inherited Retinal Disorder 51 0.038
785
DWR001 Dwarfism 44 0.038
786
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.038
787
MTB004 Metabolic Acidosis 50 0.037
788
MCR004 Macroglobulinemia 49 0.037
789
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.037
790
ALL010 Allergic Contact Dermatitis 56 0.037
791
OCL006 Ocular Hypertension 53 0.037
792
ACT017 Acute Chest Syndrome 51 0.037
793
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.037
794
P FML018 Familial Mediterranean Fever 73 0.037
795
P ORT004 Orthostatic Intolerance 62 0.037
796
INT002 Intermittent Claudication 61 0.037
797
IRN001 Iron Deficiency Anemia 59 0.037
798
P PRC019 Precocious Puberty 46 0.037
799
TTH006 Tooth Disease 46 0.037
800
P MYC033 Myoclonus 46 0.037
801
URL001 Urolithiasis 45 0.037
802
c MCR129 Microvascular Complications of Diabetes 1 66 0.037
803
P CCK001 Cockayne Syndrome 66 0.037
804
BRS099 Breast Ductal Carcinoma 62 0.037
805
P EHL001 Ehlers-Danlos Syndrome 58 0.037
806
TNS005 Tonsillitis 57 0.037
807
AVD001 Avoidant Personality Disorder 51 0.037
808
c SVR005 Severe Pre-Eclampsia 50 0.037
809
OPT003 Opiate Dependence 50 0.037
810
ADR016 Adrenal Cortical Carcinoma 48 0.037
811
c INH020 Inherited Metabolic Disorder 47 0.037
812
CRT015 Carotid Artery Occlusion 45 0.037
813
c BCT013 Bacterial Pneumonia 48 0.037
814
P PRG013 Paraganglioma 52 0.037
815
FBR054 Fibroma 44 0.037
816
P RRT020 Rare Tumor 41 0.037
817
P MLT074 Multiple Endocrine Neoplasia 56 0.036
818
P CRC039 Coarctation of Aorta 47 0.036
819
P ATR010 Atrial Heart Septal Defect 60 0.036
820
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.036
821
P GLM040 Glioma Susceptibility 1 81 0.036
822
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.036
823
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.036
824
P HRD011 Hereditary Spherocytosis 60 0.036
825
INC002 Inclusion Body Myositis 58 0.036
826
VTM002 Vitamin B12 Deficiency 48 0.036
827
P BNG030 Benign Ependymoma 60 0.036
828
HPT019 Hepatic Encephalopathy 60 0.036
829
SCH003 Schizophreniform Disorder 56 0.036
830
PRS047 Prostatitis 56 0.036
831
SLC006 Silicosis 56 0.036
832
NRN004 Neuroendocrine Tumor 55 0.036
833
CLL010 Cellular Ependymoma 54 0.036
834
P RNL017 Renal Oncocytoma 53 0.036
835
CHR073 Choreatic Disease 52 0.036
836
OST011 Osteomalacia 52 0.036
837
P CMP008 Compartment Syndrome 49 0.036
838
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.036
839
ATN005 Autonomic Dysfunction 46 0.036
840
IRR002 Irritable Bowel Syndrome 65 0.036
841
GLS018 Glass Syndrome 57 0.036
842
FND002 Fundus Dystrophy 55 0.036
843
P FRG001 Fragile X Syndrome 70 0.036
844
MNT001 Mantle Cell Lymphoma 69 0.036
845
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.036
846
LGN006 Legionnaire Disease 52 0.036
847
THY125 Thyroid Gland Medullary Carcinoma 50 0.036
848
LRN003 Learning Disability 49 0.036
849
BNN003 Bone Inflammation Disease 48 0.036
850
KLD004 Keloid Disorder 40 0.036
851
CHL039 Choledocholithiasis 38 0.036
852
CLR030 Clear Cell Renal Cell Carcinoma 53 0.035
853
ALC009 Alcoholic Liver Cirrhosis 53 0.035
854
CLR109 Colorectal Adenocarcinoma 51 0.035
855
PST021 Postpartum Depression 50 0.035
856
P FRN006 Frontotemporal Dementia 68 0.035
857
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.035
858
SDD001 Sudden Infant Death Syndrome 61 0.035
859
GRD007 Grade Iii Astrocytoma 59 0.035
860
c CHL119 Cholangitis, Primary Sclerosing 57 0.035
861
JPN002 Japanese Encephalitis 57 0.035
862
LST001 Listeriosis 56 0.035
863
ESP002 Esophageal Varix 51 0.035
864
P SCL009 Sclerosing Cholangitis 48 0.035
865
ANG020 Angiosarcoma 64 0.035
866
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.035
867
TBR011 Tuberculous Meningitis 48 0.035
868
MST019 Mastoiditis 43 0.035
869
GRM010 Germ Cells Tumors 34 0.035
870
NRM005 Neuromuscular Disease 64 0.035
871
MDS022 Mediastinitis 46 0.035
872
CYS009 Cystadenoma 44 0.035
873
c CHR682 Chronic Bilirubin Encephalopathy 39 0.035
874
EXP004 Exophthalmos 52 0.035
875
LNG108 Langerhans Cell Histiocytosis 58 0.035
876
P NJM001 Nijmegen Breakage Syndrome 74 0.035
877
P ESS003 Essential Thrombocythemia 68 0.035
878
BLD131 Bladder Urothelial Carcinoma 62 0.035
879
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.035
880
ALC006 Alcoholic Hepatitis 61 0.035
881
DBT010 Diabetic Neuropathy 54 0.035
882
P ACT008 Actinic Keratosis 53 0.035
883
ADN001 Adenosine Deaminase Deficiency 47 0.035
884
NWB001 Newborn Respiratory Distress Syndrome 58 0.034
885
HPT046 Hepatic Veno-Occlusive Disease 56 0.034
886
HPR003 Heparin-Induced Thrombocytopenia 48 0.034
887
NWC001 Newcastle Disease 45 0.034
888
LPT001 Leptospirosis 66 0.034
889
NRF007 Neurofibroma 64 0.034
890
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.034
891
SBC001 Subacute Sclerosing Panencephalitis 56 0.034
892
MYL001 Myelitis 51 0.034
893
RGH001 Right Bundle Branch Block 48 0.034
894
P MJR007 Major Affective Disorder 1 43 0.034
895
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.034
896
P PLY041 Polymyositis 57 0.034
897
EXS001 Exostosis 46 0.034
898
P GCH001 Gaucher's Disease 63 0.034
899
P SHR029 Short Syndrome 63 0.034
900
CRC006 Carcinoid Syndrome 55 0.034
901
GNG003 Gingival Recession 44 0.034
902
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.034
903
P CRB088 Cerebral Atrophy 37 0.034
904
WST001 West Syndrome 61 0.034
905
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.034
906
BLL006 Bullous Pemphigoid 62 0.034
907
LYM027 Lymphopenia 58 0.034
908
CHK001 Chikungunya 57 0.034
909
TCK001 Tick-Borne Encephalitis 56 0.034
910
P PTT006 Pituitary Adenoma 55 0.034
911
FBR009 Fibrous Dysplasia 48 0.034
912
c DRR009 Diarrhea 6 46 0.034
913
HRN029 Hearing Loss, Noise-Induced 37 0.034
914
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.034
915
HRP008 Herpes Simiae 25 0.034
916
P LNG028 Long Qt Syndrome 66 0.034
917
P AGM001 Agammaglobulinemia 65 0.034
918
PPL049 Papillon-Lefevre Syndrome 65 0.034
919
MSC007 Muscle Hypertrophy 64 0.034
920
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.034
921
DFF036 Differentiated Thyroid Carcinoma 52 0.034
922
SCH012 Schizoaffective Disorder 50 0.034
923
P OPT006 Optic Nerve Disease 60 0.033
924
P PSD015 Pseudohypoparathyroidism 56 0.033
925
P MYT002 Myotonic Dystrophy 49 0.033
926
EPC002 Epicondylitis 41 0.033
927
ADR004 Adrenal Cortical Adenocarcinoma 39 0.033
928
PRM329 Premature Aging 35 0.033
929
BHC003 Behcet Syndrome 71 0.033
930
MCC012 Mccune-Albright Syndrome 70 0.033
931
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 56 0.033
932
INT078 Intracranial Thrombosis 49 0.033
933
P CHR071 Charcot-Marie-Tooth Disease 65 0.033
934
P CHR285 Chronic Myelomonocytic Leukemia 60 0.033
935
CND002 Conduct Disorder 51 0.033
936
MTR010 Mature Teratoma 44 0.033
937
TRP009 Triple X Syndrome 42 0.033
938
GST020 Gastric Antral Vascular Ectasia 41 0.033
939
P DYS005 Dyslexia 40 0.033
940
CLF004 Cleft Lip/palate 54 0.033
941
ECT026 Ectopic Pregnancy 50 0.033
942
c DPH024 Diaphragmatic Hernia, Congenital 63 0.033
943
P ACR001 Aicardi-Goutieres Syndrome 62 0.033
944
ANG005 Anogenital Venereal Wart 55 0.033
945
c TBR025 Tuberous Sclerosis 1 77 0.032
946
P CHR012 Chronic Granulomatous Disease 67 0.032
947
P MLG056 Malignant Hyperthermia 67 0.032
948
c FML021 Familial Hypercholesterolemia 66 0.032
949
MRK001 Merkel Cell Carcinoma 65 0.032
950
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.032
951
P LYM033 Lymphoproliferative Syndrome 59 0.032
952
PLL012 Pollen Allergy 46 0.032
953
CRB079 Cerebrospinal Fluid Leak 35 0.032
954
BRN028 Brain Cancer 74 0.032
955
LNG039 Lung Squamous Cell Carcinoma 66 0.032
956
APN008 Apnea, Obstructive Sleep 64 0.032
957
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.032
958
P TCD001 Tic Disorder 53 0.032
959
P LCT001 Lactic Acidosis 51 0.032
960
CYS014 Cystadenocarcinoma 51 0.032
961
CRV040 Cervix Carcinoma 51 0.032
962
RTC005 Reticulosarcoma 47 0.032
963
c GCH015 Gaucher Disease, Type I 70 0.032
964
PCK003 Pick Disease of Brain 68 0.032
965
BLM001 Bloom Syndrome 67 0.032
966
CRP001 Carpal Tunnel Syndrome 67 0.032
967
ALV005 Alveolar Soft Part Sarcoma 61 0.032
968
EXT034 Extrinsic Allergic Alveolitis 58 0.032
969
c PSR023 Psoriasis 1 52 0.032
970
P OBS001 Obstructive Jaundice 50 0.032
971
MTC005 Mitochondrial Metabolism Disease 49 0.032
972
P CTN015 Cutaneous T Cell Lymphoma 49 0.032
973
IGG001 Iga Glomerulonephritis 48 0.032
974
CLF056 Cleft Lip with or Without Cleft Palate 47 0.032
975
P CLL015 Collagen Disease 47 0.032
976
URT010 Ureteral Obstruction 45 0.032
977
FCT007 Factor Vii Deficiency 67 0.032
978
MXD005 Mixed Connective Tissue Disease 58 0.032
979
CHR100 Chronic Ulcer of Skin 55 0.032
980
HLL004 Hellp Syndrome 54 0.032
981
P INT068 Intestinal Disease 53 0.032
982
STT041 Stuttering 52 0.032
983
CCN002 Cocaine Abuse 49 0.032
984
PLC007 Placental Abruption 48 0.032
985
EPD015 Epidemic Typhus 45 0.032
986
CND006 Candida Glabrata 32 0.032
987
PNM001 Pneumocystosis 59 0.032
988
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.032
989
BRT054 Brittle Bone Disorder 72 0.032
990
ADN011 Adenoid Cystic Carcinoma 70 0.032
991
P DRM010 Dermatomyositis 61 0.032
992
c LPM012 Lipomatosis, Multiple 60 0.032
993
PYD001 Pyoderma Gangrenosum 54 0.032
994
HMP001 Hemopericardium 48 0.032
995
CRT072 Creutzfeldt-Jakob Disease 70 0.032
996
P USH001 Usher Syndrome 60 0.032
997
P SPN052 Spondyloarthropathy 54 0.032
998
MRG003 Marginal Zone B-Cell Lymphoma 52 0.032
999
SPS003 Spastic Diplegia 51 0.032
1000
ANR004 Anuria 46 0.032
1001
MLD001 Melioidosis 68 0.031
1002
HYP020 Hyperprolactinemia 64 0.031
1003
PTN001 Patent Foramen Ovale 60 0.031
1004
MCR013 Microphthalmia 57 0.031
1005
P PNM006 Pneumoconiosis 56 0.031
1006
AMB001 Amebiasis 55 0.031
1007
PLV003 Pelvic Inflammatory Disease 55 0.031
1008
HRY003 Hairy Cell Leukemia 55 0.031
1009
ACH005 Achalasia 51 0.031
1010
ASP003 Aseptic Meningitis 51 0.031
1011
P ESN008 Eosinophilic Pneumonia 50 0.031
1012
AMB002 Amblyopia 49 0.031
1013
ANT018 Anthracosis 48 0.031
1014
P VTR007 Vitreoretinopathy 46 0.031
1015
ACT003 Acute Kidney Tubular Necrosis 45 0.031
1016
CRN322 Coronavirus Infectious Disease 40 0.031
1017
HPR006 Heparin Cofactor Ii Deficiency 40 0.031
1018
SPP007 Suppression Amblyopia 39 0.031
1020
LYM007 Lymphangioleiomyomatosis 69 0.031
1021
PLM070 Pulmonic Stenosis 57 0.031
1022
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.031
1023
CHR177 Chromophobe Renal Cell Carcinoma 57 0.031
1024
GST050 Gastrointestinal System Disease 56 0.031
1025
FCL014 Focal Epilepsy 54 0.031
1026
BCT002 Bacterial Vaginosis 53 0.031
1027
c PRM108 Primary Progressive Multiple Sclerosis 51 0.031
1028
PLR008 Pleurisy 50 0.031
1029
BLR001 Biliary Atresia 50 0.031
1030
URT001 Urethritis 49 0.031
1031
RNL077 Renal Fibrosis 47 0.031
1032
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.031
1033
RDN001 Reading Disorder 40 0.031
1034
GST019 Gastrointestinal Stromal Tumor 78 0.030
1035
P TYS001 Tay-Sachs Disease 69 0.030
1036
PNM010 Pneumothorax, Primary Spontaneous 60 0.030
1037
P LKD001 Leukodystrophy 59 0.030
1038
CRY005 Cryptococcosis 58 0.030
1039
HDR002 Hidradenitis Suppurativa 55 0.030
1040
MYL020 Myelomeningocele 51 0.030
1041
HDR003 Hidradenitis 49 0.030
1042
ANG018 Angiomyolipoma 46 0.030
1043
PLM005 Pleomorphic Lipoma 40 0.030
1044
RTR011 Retroperitoneal Fibrosis 40 0.030
1045
HRL003 Hurler Syndrome 65 0.030
1046
CLC001 Calciphylaxis 51 0.030
1047
STR008 Strongyloidiasis 51 0.030
1048
P BCT020 Bacteremia 2 44 0.030
1049
SPC005 Speech Disorder 43 0.030
1050
ORL012 Oral Leukoplakia 39 0.030
1051
AYM001 Ayme-Gripp Syndrome 57 0.030
1052
P VNS003 Venous Insufficiency 55 0.030
1053
GLS001 Gliosarcoma 54 0.030
1054
P ICH004 Ichthyosis 54 0.030
1055
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.030
1056
KRT001 Keratoconjunctivitis Sicca 49 0.030
1057
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.030
1058
CHL147 Chlamydia Pneumonia 48 0.030
1059
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.030
1060
PRP007 Priapism 47 0.030
1061
RTN020 Retinal Vascular Disease 46 0.030
1062
c DRM054 Dermatitis, Atopic, 2 44 0.030
1063
DMP001 Dumping Syndrome 44 0.030
1064
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.030
1065
PRM020 Premenstrual Tension 40 0.030
1066
SCR011 Scrapie 39 0.030
1067
STR077 Streptococcal Toxic-Shock Syndrome 37 0.030
1068
LBR036 Leber Plus Disease 66 0.030
1069
P MST009 Mastocytosis 64 0.030
1070
HMT002 Hematologic Cancer 62 0.030
1071
NRN001 Neuroendocrine Carcinoma 47 0.030
1072
c TRC022 Tricuspid Valve Insufficiency 45 0.030
1073
MCR011 Microinvasive Gastric Cancer 43 0.030
1074
GRM004 Germinoma 40 0.030
1075
CYT018 Cytochrome P450 2d6 Variant 27 0.030
1076
c HRD010 Hereditary Spastic Paraplegia 66 0.029
1077
CMM004 Common Variable Immunodeficiency 68 0.029
1078
MYL031 Myeloproliferative Neoplasm 66 0.029
1079
P LPS002 Liposarcoma 65 0.029
1080
P TST021 Testicular Germ Cell Tumor 60 0.029
1081
TRG002 Trigeminal Neuralgia 60 0.029
1082
LYM021 Lymphadenitis 57 0.029
1083
MCP006 Mucoepidermoid Carcinoma 50 0.029
1084
c HRD026 Hereditary Ataxia 48 0.029
1085
GRW007 Growth Hormone Deficiency 46 0.029