Search results for tannic acid

1414 hits were found for tannic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.275
2
P LVR013 Liver Disease 71 0.262
3
FTT001 Fatty Liver Disease 63 0.230
4
CHL068 Cholestasis 61 0.228
5
LVR012 Liver Cirrhosis 67 0.225
6
P CLR023 Colorectal Cancer 100 0.222
7
ACT119 Acute Promyelocytic Leukemia 63 0.207
8
HLX001 Helix Syndrome 46 0.204
9
P NRB010 Neuroblastoma 1 66 0.201
10
NRL016 Neural Tube Defects 83 0.200
11
P KDN018 Kidney Disease 73 0.200
12
MTB004 Metabolic Acidosis 48 0.198
13
P SZR006 Seizure Disorder 59 0.195
14
P DRR001 Diarrhea 55 0.195
15
VSL002 Visual Epilepsy 58 0.189
16
48X005 48,xyyy 37 0.189
17
P DDN001 Duodenal Ulcer 50 0.186
18
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.185
19
OST012 Osteoarthritis 80 0.181
20
P BRS047 Breast Cancer 99 0.181
21
LPD008 Lipid Metabolism Disorder 64 0.181
22
GST092 Gastroesophageal Reflux 68 0.180
23
CLT003 Colitis 63 0.179
24
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.179
25
P GLM045 Glioma 64 0.178
26
GLL048 Glial Tumor 48 0.176
27
BNR002 Bone Resorption Disease 51 0.175
28
P PRS040 Prostate Cancer 97 0.171
29
ISC004 Ischemia 62 0.170
30
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.168
31
P CRN300 Coronary Heart Disease 1 59 0.167
32
PLM017 Pulmonary Alveolar Microlithiasis 54 0.166
33
P NRF023 Neurofibromatosis, Type Ii 77 0.163
34
ATH013 Atherosclerosis Susceptibility 68 0.162
35
ULC004 Ulcerative Colitis 75 0.160
36
P HPT023 Hepatocellular Carcinoma 99 0.159
37
P INF037 Inflammatory Bowel Disease 57 0.159
38
P ENC018 Encephalopathy 64 0.158
39
ALL026 Allergic Hypersensitivity Disease 65 0.158
40
P HYP750 Hypertriglyceridemia, Familial 62 0.157
41
HYP066 Hyperglycemia 63 0.156
42
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.156
43
PRM236 Primary Biliary Cholangitis 57 0.154
44
DRM006 Dermatitis 63 0.154
45
P LKM002 Leukemia 69 0.154
46
P PSR002 Psoriasis 63 0.154
47
PPT005 Peptic Ulcer Disease 60 0.153
48
c GLL024 Gallbladder Disease 1 53 0.153
49
HYP056 Hypoglycemia 68 0.153
50
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.150
51
PRT037 Pertussis 66 0.150
52
P OST002 Osteoporosis 79 0.149
53
c HYP836 Hypercholesterolemia, Familial, 1 74 0.147
54
P VSC007 Vascular Disease 65 0.147
55
PST011 Pustulosis of Palm and Sole 51 0.146
56
P ADN016 Adenocarcinoma 65 0.146
57
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.146
58
GLB002 Glioblastoma 74 0.145
59
P CRN018 Coronary Artery Anomaly 67 0.145
60
GLB015 Glioblastoma Multiforme 60 0.145
61
P PRM006 Primary Biliary Cirrhosis 54 0.144
62
c CHR684 Chronic Kidney Disease 68 0.144
63
PLM001 Pulmonary Tuberculosis 72 0.143
64
CYS001 Cystic Fibrosis 84 0.143
65
DFC004 Deficiency Anemia 77 0.143
66
P HNT016 Huntington Disease 72 0.143
67
ADN018 Adenoma 60 0.143
68
c ACT210 Acute Respiratory Distress Syndrome 59 0.143
69
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.141
70
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.141
71
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.141
72
P OVR042 Ovarian Cancer 89 0.140
73
HMN044 Human Immunodeficiency Virus Type 1 73 0.139
74
ATM095 Autoimmune Disease 62 0.139
75
P GST044 Gastritis 58 0.139
76
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.138
77
P ALZ034 Alzheimer Disease 90 0.138
78
HYP060 Hyperinsulinism 55 0.137
79
ART140 Arteries, Anomalies of 60 0.136
80
P HRT032 Heart Disease 78 0.135
81
P DBT009 Diabetes Mellitus 66 0.135
82
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.135
83
P PNC035 Pancreatic Cancer 86 0.134
84
P ESP024 Esophagitis 62 0.133
85
GST023 Gastric Ulcer 53 0.133
86
P MYL006 Myeloid Leukemia 61 0.133
87
HRW001 Hair Whorl 36 0.132
88
c HPT073 Hepatitis C Virus 74 0.131
89
DPR016 Depression 64 0.131
90
P LNG032 Lung Cancer 99 0.130
91
HPT004 Hepatic Coma 42 0.130
92
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.130
93
c HYP595 Hypertension, Essential 87 0.128
94
47X002 47,xyy 49 0.128
95
OCL069 Ocular Motor Apraxia 53 0.128
96
NNL006 Non-Alcoholic Steatohepatitis 53 0.128
97
P BLD134 Bladder Cancer 79 0.128
98
c LKM061 Leukemia, Acute Myeloid 84 0.128
99
P BPL003 Bipolar Disorder 59 0.127
100
P HRP006 Herpes Simplex 66 0.127
101
c MJR024 Major Affective Disorder 9 42 0.127
102
c MJR022 Major Affective Disorder 8 39 0.127
103
HYP266 Hypoxia 58 0.125
104
CYT002 Cytokine Deficiency 46 0.125
105
P NRP001 Neuropathy 57 0.124
106
P LYM031 Lymphocytic Leukemia 56 0.123
107
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.123
108
P MYC007 Myocardial Infarction 74 0.123
109
MYL069 Myeloma, Multiple 85 0.121
110
MNT002 Mental Depression 60 0.121
111
HPT019 Hepatic Encephalopathy 60 0.121
112
P DRM053 Dermatitis, Atopic 68 0.121
113
PHN003 Phenylketonuria 73 0.120
114
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.120
115
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.120
116
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.120
117
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.120
118
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.120
119
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.120
120
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.120
121
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.120
122
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.120
123
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.120
124
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.119
125
CRH001 Crohn's Disease 75 0.119
126
OST159 Osteogenic Sarcoma 67 0.119
127
SPN186 Spinal Cord Injury 63 0.119
128
P CHL066 Cholangitis 53 0.119
129
CRB039 Cerebrovascular Disease 71 0.118
130
SKN016 Skin Disease 64 0.118
131
INS024 Insulin-Like Growth Factor I 79 0.118
132
CHL014 Cholera 58 0.118
133
PPL052 Papillomatosis, Confluent and Reticulated 34 0.118
134
P ATS364 Autism 68 0.117
135
BND020 Bone Disease 60 0.117
136
HYP781 Hypoascorbemia 48 0.117
137
END030 End Stage Renal Failure 60 0.117
138
DYS014 Dyspepsia 51 0.117
139
c ACT071 Acute Kidney Failure 60 0.115
140
BRN071 Brain Injury 51 0.115
141
P GST053 Gastric Cancer 85 0.114
142
P NTR004 Neutropenia 64 0.114
143
c PCH010 Pachyonychia Congenita 3 43 0.114
144
LNG099 Lung Disease 62 0.114
145
CNG034 Congestive Heart Failure 69 0.113
146
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.113
147
NTR005 Nutritional Deficiency Disease 61 0.113
148
P MYP004 Myopathy 63 0.112
149
c RHB024 Rhabdomyosarcoma 2 64 0.112
150
CRV035 Cervical Cancer 77 0.112
151
ALC007 Alcohol Dependence 68 0.112
152
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.112
153
URM002 Uremia 50 0.111
154
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.111
155
STR067 Stroke, Ischemic 82 0.111
156
c ACT075 Acute Myocardial Infarction 59 0.110
157
P RHM011 Rheumatoid Arthritis 82 0.110
158
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.110
159
P LTR001 Lateral Sclerosis 56 0.109
160
BCT022 Bacterial Infectious Disease 57 0.109
161
BRR014 Barrett Esophagus 67 0.109
162
SQM006 Squamous Cell Carcinoma 60 0.109
163
ADR007 Adrenoleukodystrophy 72 0.109
164
P HYP086 Hypothyroidism 70 0.109
165
TRM010 Traumatic Brain Injury 54 0.108
166
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.108
167
STM007 Stomatitis 51 0.108
168
P INF038 Influenza 69 0.107
169
THR024 Thrombosis 58 0.107
170
GLC003 Glucose Intolerance 55 0.107
171
P SKN015 Skin Carcinoma 67 0.107
172
ADR022 Adrenomyeloneuropathy 39 0.106
173
CRB004 Cerebral Artery Occlusion 38 0.106
174
c MCR120 Microvascular Complications of Diabetes 7 48 0.106
175
c MCR113 Microvascular Complications of Diabetes 3 55 0.106
176
P EPL164 Epilepsy 73 0.105
177
c MGR028 Migraine with or Without Aura 1 70 0.105
178
P PRD008 Periodontitis 66 0.105
179
P TRN020 Turner Syndrome 66 0.105
180
c MCR130 Microvascular Complications of Diabetes 6 42 0.105
181
c MCR133 Microvascular Complications of Diabetes 4 42 0.105
182
P ART022 Arthritis 71 0.105
183
HMP009 Haemophilus Influenzae 46 0.105
184
CNS004 Constipation 59 0.105
185
P MPL001 Maple Syrup Urine Disease 68 0.104
186
c HPT001 Hepatitis C 62 0.104
187
c ATS007 Autism Spectrum Disorder 69 0.103
188
P CTR002 Cataract 62 0.103
189
PLM033 Pulmonary Embolism 60 0.103
190
P SCH015 Schizophrenia 76 0.103
191
AGN016 Aging 58 0.102
192
CHL123 Chlamydia 60 0.102
193
P MJR001 Major Depressive Disorder 69 0.101
194
KRT009 Keratosis 52 0.101
195
c ACT068 Acute Cystitis 63 0.101
196
P BCL017 B-Cell Lymphoma 61 0.100
197
c SYS001 Systemic Lupus Erythematosus 88 0.100
198
RCK004 Rickets 70 0.100
199
c ACT027 Acute Pancreatitis 60 0.099
200
VCC001 Vaccinia 50 0.099
201
P HPT021 Hepatitis 69 0.099
202
MLN008 Melanoma 68 0.099
203
P RSP003 Respiratory Failure 75 0.099
204
CLN015 Colon Adenocarcinoma 65 0.099
205
BRN024 Bronchitis 70 0.098
206
P THR014 Thrombocytopenia 67 0.098
207
PLM010 Pulmonary Edema 56 0.098
208
c THR092 Thrombophilia Due to Thrombin Defect 74 0.098
209
P PRP019 Peripheral Nervous System Disease 64 0.098
210
P CRD132 Cardiac Conduction Defect 61 0.097
211
P ART021 Arteriosclerosis 56 0.097
212
P MLT020 Multiple Sclerosis 73 0.097
213
IMM167 Immune Deficiency Disease 79 0.096
214
HLC007 Helicobacter Pylori Infection 61 0.096
215
OVR082 Overgrowth Syndrome 51 0.096
217
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.096
218
P ENC004 Encephalitis 64 0.096
219
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.096
220
P MNN013 Meningitis 67 0.096
221
PRT036 Peritonitis 66 0.096
222
HYP005 Hypokalemia 55 0.096
223
PPT001 Peptic Esophagitis 47 0.096
224
c SML038 Small Cell Cancer of the Lung 67 0.095
225
ESP021 Esophageal Cancer 90 0.095
226
P LPS004 Lupus Erythematosus 62 0.095
227
P RHN004 Rhinitis 59 0.095
228
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.095
229
THY029 Thyroid Carcinoma 62 0.095
230
P PRP029 Porphyria 58 0.095
231
ALL014 Allergic Encephalomyelitis 40 0.095
232
LYS012 Lysosomal Acid Lipase Deficiency 63 0.094
233
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.094
234
c VRL010 Viral Hepatitis 56 0.094
235
MYL009 Myelodysplastic Syndrome 72 0.094
236
P MSC005 Muscular Dystrophy 68 0.094
237
c GLY008 Glycogen Storage Disease Ii 68 0.093
238
P PNC044 Pancreatitis 61 0.093
239
SRC014 Sarcoma 67 0.093
240
SPN035 Spindle Cell Sarcoma 57 0.093
241
TTN003 Tetanus 62 0.093
242
P AST007 Astrocytoma 52 0.093
243
c MLG068 Malignant Glioma 46 0.093
244
PRS045 Prostatic Hypertrophy 55 0.093
245
P MSC003 Muscular Atrophy 52 0.092
246
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.092
247
MDD011 Mood Disorder 62 0.092
248
P GLM007 Glomerulonephritis 58 0.092
249
CLF027 Cleft Palate, Isolated 67 0.091
250
RHM027 Rheumatic Disease 56 0.091
251
DBT010 Diabetic Neuropathy 56 0.091
252
PPL022 Papilloma 56 0.091
253
P LYM118 Lymphoma 70 0.091
254
CHL004 Cholelithiasis 50 0.091
255
ACQ007 Acquired Immunodeficiency Syndrome 61 0.090
256
CHL079 Children's Interstitial Lung Disease 27 0.090
257
GST045 Gastroenteritis 60 0.090
258
DNT012 Dental Caries 52 0.090
259
P PHC003 Pheochromocytoma 71 0.090
260
KRT002 Keratomalacia 47 0.090
261
c ACT073 Acute Leukemia 59 0.090
262
PRX001 Peroxisomal Disease 45 0.090
263
P PLM036 Pulmonary Fibrosis 66 0.089
264
IDP011 Idiopathic Interstitial Pneumonia 65 0.089
265
ADR040 Adrenal Gland Pheochromocytoma 51 0.089
266
ATX019 Ataxia with Vitamin E Deficiency 46 0.089
267
P EXN002 Exanthem 58 0.089
268
P CYS018 Cystitis 59 0.089
269
MTH071 Methane Production 26 0.089
270
ANG054 Angina Pectoris 66 0.089
271
P TRM003 Tremor 55 0.089
272
P GLY013 Glycogen Storage Disease 59 0.089
273
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.088
274
P FBR017 Fibrosarcoma 57 0.088
275
P HYP076 Hyperthyroidism 55 0.088
276
ANX010 Anxiety 75 0.088
277
P ATR011 Atrial Fibrillation 67 0.088
278
CHL065 Cholangiocarcinoma 68 0.088
279
MCS002 Mucositis 56 0.088
280
SQM002 Squamous Cell Papilloma 49 0.088
281
P INF032 Infertility 60 0.087
282
c LRG017 Large Intestine Cancer 53 0.087
283
GST033 Gestational Diabetes 58 0.087
284
P CRD119 Cardiac Arrest 71 0.087
285
SVR004 Severe Combined Immunodeficiency 74 0.087
286
INT079 Intrahepatic Cholangiocarcinoma 54 0.087
287
P ALP008 Alopecia 58 0.086
288
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.086
289
P PLY019 Polyneuropathy 55 0.086
290
P ALC033 Alcohol Use Disorder 58 0.085
291
P PNM007 Pneumonia 71 0.084
292
AST005 Asthma 80 0.084
293
MTH009 Mouth Disease 56 0.084
294
c HPT016 Hepatitis B 63 0.083
295
PRS021 Prostatic Adenoma 52 0.083
296
P GCH001 Gaucher's Disease 63 0.082
297
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.082
298
HMS001 Hemosiderosis 54 0.082
299
P CNR004 Cone-Rod Dystrophy 2 72 0.082
300
P LKM062 Leukemia, Acute Lymphoblastic 68 0.082
301
P INS002 in Situ Carcinoma 55 0.082
302
P HMR005 Hemorrhoid 47 0.082
303
P DMN002 Dementia 68 0.082
304
c FNC043 Fanconi Anemia, Complementation Group E 64 0.081
305
c PRS136 Prostate Cancer, Hereditary, 6 34 0.081
306
c PRS130 Prostate Cancer, Hereditary, 8 33 0.081
307
P AMY004 Amyloidosis 71 0.081
308
c ATR087 Atrial Standstill 1 76 0.081
309
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.081
310
P MYC084 Mycobacterium Tuberculosis 1 69 0.081
311
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.081
312
PRS129 Prostatic Hyperplasia, Benign 49 0.081
313
IRR002 Irritable Bowel Syndrome 65 0.080
314
GST050 Gastrointestinal System Disease 57 0.080
315
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.080
316
ALL003 Allergic Rhinitis 69 0.080
317
P RRH023 Rare Hereditary Hemochromatosis 41 0.080
318
ENT004 Enthesopathy 46 0.080
319
P CHR345 Chronic Pain 52 0.080
320
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.079
321
P HDC001 Headache 59 0.079
322
PRP027 Peripheral Vascular Disease 72 0.079
323
DPH001 Diphtheria 61 0.078
324
P ART023 Arthropathy 61 0.078
325
LPT014 Leptin Deficiency or Dysfunction 72 0.078
326
P PLY011 Polycystic Ovary Syndrome 58 0.078
327
INT007 Intermediate Coronary Syndrome 58 0.078
328
c LKM071 Leukemia, Chronic Lymphocytic 81 0.078
329
P URT039 Urticaria 61 0.077
330
ORL011 Oral Cancer 62 0.077
331
RSC001 Rosacea 55 0.077
332
ENT011 Enterocolitis 51 0.077
333
P NPH012 Nephrotic Syndrome 65 0.077
334
P NSP012 Nasopharyngeal Carcinoma 67 0.076
335
P HYP098 Hypereosinophilic Syndrome 67 0.076
336
P RCT021 Rectum Cancer 54 0.076
337
EYD002 Eye Disease 59 0.076
338
P HYP069 Hyperparathyroidism 64 0.076
339
BLR008 Bilirubin Metabolic Disorder 58 0.076
340
ATS010 Autosomal Recessive Disease 49 0.076
341
LSH001 Leishmaniasis 64 0.075
342
P KLZ004 Kala-Azar 1 43 0.075
343
LYM019 Lymphosarcoma 48 0.075
344
c LKM004 Leukemia, B-Cell, Chronic 35 0.075
345
INS001 Insulinoma 60 0.075
346
P RTN016 Retinal Degeneration 56 0.074
347
MLR004 Malaria 82 0.074
348
P THL005 Thalassemia 62 0.074
349
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.074
350
PRT013 Portal Hypertension 61 0.074
351
P PRK057 Parkinson Disease, Late-Onset 77 0.073
352
BRN028 Brain Cancer 75 0.073
353
END057 Endometrial Cancer 74 0.073
354
PLY150 Polykaryocytosis Inducer 31 0.073
355
c BSL007 Basal Cell Carcinoma 68 0.073
356
c LKM063 Leukemia, Chronic Myeloid 74 0.073
357
c GCH015 Gaucher Disease, Type I 65 0.073
358
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.072
359
c HPT003 Hepatitis a 60 0.072
360
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.072
361
HYP081 Hypolipoproteinemia 51 0.072
362
MMM001 Mammary Paget's Disease 53 0.071
363
P CND004 Candidiasis 61 0.071
364
IRN001 Iron Deficiency Anemia 59 0.071
365
P BNG032 Benign Mesothelioma 47 0.071
366
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.070
367
LNG031 Lung Benign Neoplasm 52 0.070
368
TRN015 Transient Cerebral Ischemia 62 0.070
369
IGR001 Ige Responsiveness, Atopic 61 0.070
370
P TCL004 T-Cell Leukemia 48 0.070
371
c LKM005 Leukemia, T-Cell, Chronic 35 0.070
372
P SYS005 Systemic Scleroderma 68 0.070
373
P END044 Endometriosis 63 0.070
374
CHR073 Choreatic Disease 52 0.069
375
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.069
376
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.069
377
ERY051 Erythroleukemia, Familial 58 0.069
378
P MDL005 Medulloblastoma 78 0.069
379
ACR006 Aceruloplasminemia 74 0.069
380
OTT002 Otitis Media 71 0.069
381
P KDN017 Kidney Cancer 60 0.068
382
P INT068 Intestinal Disease 56 0.068
383
PRN019 Perinatal Necrotizing Enterocolitis 55 0.068
384
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.068
385
P GRF003 Graft-Versus-Host Disease 71 0.068
386
PSY004 Psychotic Disorder 68 0.068
387
c PNS012 Paine Syndrome 61 0.068
388
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.068
389
P GLM040 Glioma Susceptibility 1 68 0.068
390
END040 Endogenous Depression 55 0.067
391
DYS073 Dysphagia 52 0.067
392
TLN003 Telangiectasis 53 0.067
393
LYS002 Lysosomal Storage Disease 52 0.067
394
c DLT002 Dilated Cardiomyopathy 81 0.067
395
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.067
396
P INT143 Interstitial Cystitis 62 0.067
397
AMN003 Amnestic Disorder 55 0.066
398
RRS014 Rare Surgical Neurologic Disease 33 0.066
399
P DYS154 Dystonia 65 0.066
400
PLM031 Poliomyelitis 58 0.066
401
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.066
402
c FML035 Familial Hyperlipidemia 56 0.066
403
SYN007 Synovitis 55 0.066
404
PNC129 Pancreatic Adenocarcinoma 69 0.066
405
SFT003 Soft Tissue Sarcoma 57 0.066
406
GNG013 Gingivitis 60 0.066
407
CMM005 Common Cold 57 0.066
408
CHL067 Cholecystitis 60 0.065
409
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.065
410
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.065
411
DYS015 Dysentery 45 0.065
412
c PRM038 Primary Agammaglobulinemia 45 0.065
413
c CHR064 Chronic Monocytic Leukemia 43 0.065
414
P SRC025 Sarcoidosis 1 72 0.064
415
LYM133 Lymphoma, Hodgkin, Classic 70 0.064
416
P END033 Endocarditis 58 0.064
417
TRN018 Transitional Cell Carcinoma 57 0.064
418
ALL006 Allergic Asthma 56 0.064
419
VRC005 Varicose Veins 61 0.064
420
P DNG005 Dengue Virus 57 0.064
421
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.064
422
HDN002 Head Injury 47 0.064
423
SBC016 Subacute Delirium 43 0.064
424
PST092 Posttransplant Acute Limbic Encephalitis 29 0.064
425
P HYD006 Hydrocephalus 68 0.064
426
c CNG216 Congenital Hydrocephalus 55 0.064
427
NRT001 Neurotic Disorder 53 0.064
428
c SCL052 Scleroderma, Familial Progressive 62 0.064
429
P PLY014 Polycystic Kidney Disease 61 0.064
430
P SCL018 Scoliosis 61 0.063
431
c PRD040 Periodontitis, Chronic 56 0.063
432
MSC007 Muscle Hypertrophy 65 0.063
433
MSC157 Muscular Dystrophy, Duchenne Type 70 0.063
434
PLG002 Plague 54 0.063
435
P SLP006 Sleep Apnea 71 0.063
436
P HYP061 Hypertrophic Cardiomyopathy 68 0.063
437
BRK010 Burkitt Lymphoma 68 0.063
438
MNN042 Meningioma, Radiation-Induced 64 0.063
439
P HMP007 Hemophilia 58 0.063
440
IGG001 Iga Glomerulonephritis 50 0.063
441
MXD026 Mixed Glioma 36 0.062
442
c MCR129 Microvascular Complications of Diabetes 1 67 0.062
443
P UVT001 Uveitis 58 0.062
444
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.062
445
c MNN043 Meningioma, Familial 74 0.062
446
SPN021 Spinal Meningioma 40 0.062
447
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.062
448
SCR001 Secretory Meningioma 38 0.062
449
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.061
450
KPS004 Kaposi Sarcoma 75 0.061
451
ANR007 Anorexia Nervosa 64 0.061
452
P VSC011 Vasculitis 64 0.061
453
c BRN108 Branchiootic Syndrome 1 62 0.061
454
HMT018 Hematopoietic Stem Cell Transplantation 54 0.061
455
PLC008 Placenta Disease 51 0.061
456
SPL018 Splenomegaly 48 0.061
457
c SPN225 Spondyloarthropathy 1 74 0.061
458
P BNC003 Bone Cancer 56 0.061
459
WTH001 Withdrawal Disorder 47 0.061
460
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.061
461
CRH005 Crohn's Colitis 56 0.061
462
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.061
463
PTT037 Pituitary Tumors 47 0.061
464
P RHB003 Rhabdomyosarcoma 62 0.060
465
ANR040 Aneurysm 60 0.060
466
PRP080 Peripheral Artery Disease 51 0.060
467
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.060
468
c GRV008 Graves Disease 1 55 0.060
469
P RTN018 Retinal Disease 53 0.060
470
P MJR007 Major Affective Disorder 1 44 0.060
471
OVR094 Ovarian Epithelial Cancer 39 0.060
472
OST017 Osteomyelitis 65 0.060
473
VSC002 Vascular Dementia 57 0.060
474
P MTH007 Methemoglobinemia 47 0.060
475
P CLC063 Celiac Disease 1 66 0.059
476
RTN017 Retinal Detachment 62 0.059
477
P ADL010 Adult Respiratory Distress Syndrome 61 0.059
478
CLF001 Cleft Lip 53 0.059
479
DSS008 Disease of Mental Health 66 0.059
480
c ATM011 Autoimmune Hepatitis 63 0.059
481
MLK006 Milk Allergy 44 0.059
482
P SPN046 Spinal Muscular Atrophy 65 0.058
483
CHC001 Chickenpox 53 0.058
484
PST021 Postpartum Depression 51 0.058
485
P ALP009 Alopecia Areata 61 0.058
486
LYM027 Lymphopenia 58 0.058
487
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.058
488
GLS001 Gliosarcoma 56 0.058
489
SPS057 Spasticity 38 0.058
490
c HYP272 Hypercholesterolemia, Familial, 3 44 0.058
491
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.058
492
c INT059 Internal Hemorrhoid 41 0.057
493
PLS011 Plasmacytoma 57 0.057
494
CRT017 Cartilage Disease 54 0.057
495
BCT002 Bacterial Vaginosis 52 0.057
496
ILS001 Ileus 51 0.057
497
HYD002 Hydronephrosis 58 0.057
498
c FML001 Familial Atrial Fibrillation 67 0.057
499
CRC021 Carcinosarcoma 62 0.056
500
KRT013 Keratolytic Winter Erythema 45 0.056
501
HYP141 Hyperphenylalaninemia 40 0.056
502
KRT019 Keratitis, Hereditary 69 0.056
503
IMP005 Impotence 53 0.056
504
SPN051 Spondylitis 53 0.056
505
HYP017 Hypophosphatemia 48 0.056
506
INF009 Inflammatory Spondylopathy 29 0.056
507
P GRV001 Graves' Disease 57 0.056
508
CRN030 Coronary Stenosis 49 0.056
509
c MJR003 Major Affective Disorder 6 34 0.056
510
c MJR006 Major Affective Disorder 5 34 0.056
511
SKN019 Skin Melanoma 68 0.055
512
P OLG002 Oligodendroglioma 67 0.055
513
P MVM001 Movement Disease 63 0.055
514
THY030 Thyroid Gland Disease 53 0.055
515
CRB037 Cerebral Palsy 69 0.055
516
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.055
517
49X002 49,xxxxy Syndrome 39 0.055
518
P MTR014 Motor Neuron Disease 66 0.055
519
FCL014 Focal Epilepsy 56 0.055
520
c MJR008 Major Affective Disorder 2 35 0.055
521
c MJR023 Major Affective Disorder 7 34 0.055
522
c MJR004 Major Affective Disorder 4 29 0.055
523
GRD007 Grade Iii Astrocytoma 59 0.054
524
P FTL001 Fetal Alcohol Syndrome 56 0.054
525
P SBS003 Substance Abuse 56 0.054
526
P PTT006 Pituitary Adenoma 53 0.054
527
SCH012 Schizoaffective Disorder 50 0.054
528
NRN004 Neuroendocrine Tumor 59 0.054
529
P ATX030 Ataxia-Telangiectasia 83 0.054
530
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.054
531
CNN005 Connective Tissue Disease 68 0.054
532
P PLY018 Polycythemia 56 0.054
533
P LCH002 Lichen Planus 55 0.054
534
c INF071 Inflammatory Bowel Disease 1 66 0.054
535
c WLM018 Wilms Tumor 5 63 0.054
536
TRD006 Tardive Dyskinesia 58 0.054
537
YLL002 Yellow Fever 58 0.054
538
c PSR017 Psoriasis 2 55 0.054
539
GLS018 Glass Syndrome 51 0.054
540
c PSR023 Psoriasis 1 50 0.054
541
c PSR028 Psoriasis 7 40 0.054
542
c PSR018 Psoriasis 13 40 0.054
543
c PSR032 Psoriasis 11 40 0.054
544
CHY002 Chylomicron Retention Disease 63 0.053
545
VRL011 Viral Infectious Disease 62 0.053
546
ACT058 Active Peptic Ulcer Disease 55 0.053
547
CRD223 Cardiac Arrhythmia 61 0.053
548
INT002 Intermittent Claudication 60 0.053
549
P SLP005 Sleep Disorder 58 0.053
550
PHR003 Pharyngitis 56 0.053
551
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.053
552
DWR001 Dwarfism 45 0.053
554
P VSC018 Visceral Steatosis 34 0.053
555
RRD056 Rare Disease in Surgical Orthopedic 29 0.053
556
LKD001 Leukodystrophy 61 0.053
557
LMY002 Leiomyoma 52 0.053
558
P PRS038 Personality Disorder 66 0.052
559
FCT007 Factor Vii Deficiency 65 0.052
560
FBR047 Fibromyalgia 60 0.052
561
PNC001 Pancytopenia 54 0.052
562
P THY032 Thyroiditis 52 0.052
563
c SCN007 Secondary Hyperparathyroidism 52 0.052
564
MNT001 Mantle Cell Lymphoma 69 0.052
565
INT075 Intracranial Hypertension 54 0.052
566
c ACT135 Acute Graft Versus Host Disease 52 0.052
567
ART016 Aortic Aneurysm 71 0.052
568
CYT008 Cytomegalovirus Infection 58 0.052
569
BRN056 Bronchopulmonary Dysplasia 57 0.052
570
NTR046 Neutrophil Migration 49 0.052
571
P MYS003 Myasthenia Gravis 68 0.051
572
PLC005 Placental Insufficiency 55 0.051
573
P PNC025 Panic Disorder 53 0.051
574
c INF145 Infantile Liver Failure Syndrome 1 50 0.051
575
c MLG074 Malignant Mesenchymoma 50 0.051
576
ANP008 Anaplastic Oligoastrocytoma 31 0.051
577
c HMC039 Hemochromatosis, Type 1 73 0.051
578
SCH003 Schizophreniform Disorder 49 0.051
579
HPT014 Hepatorenal Syndrome 49 0.051
580
c EXD008 Exudative Vitreoretinopathy 1 69 0.050
581
P TRC086 Trichohepatoenteric Syndrome 1 57 0.050
582
HMG005 Hemoglobinopathy 57 0.050
583
P ANG015 Angioedema 54 0.050
584
BCK006 Back Pain 44 0.050
585
CCC002 Coccidiosis 46 0.050
586
CHR066 Chronic Fatigue Syndrome 61 0.050
587
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.050
588
P TBR001 Tuberous Sclerosis 72 0.050
589
ACR007 Acromegaly 70 0.050
590
c MST023 Mesothelioma, Malignant 59 0.050
591
P MTC069 Mitochondrial Disorders 57 0.050
592
PRP016 Paraplegia 54 0.050
593
PTH003 Pathologic Nystagmus 53 0.050
594
c MCR112 Microvascular Complications of Diabetes 2 42 0.050
595
P MYP006 Myopia 58 0.049
596
LYM040 Lymphoblastic Lymphoma 54 0.049
597
P CLL015 Collagen Disease 46 0.049
598
c CHR682 Chronic Bilirubin Encephalopathy 36 0.049
599
MLT157 Multiple System Atrophy 1 71 0.049
600
EWN003 Ewing Sarcoma 69 0.049
601
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.049
602
HMT002 Hematologic Cancer 64 0.049
603
ETN001 Eating Disorder 61 0.049
604
THY122 Thyroid Gland Cancer 59 0.049
605
P PMP001 Pemphigus 56 0.049
606
c PRM005 Primary Hyperparathyroidism 60 0.049
607
P INT070 Intestinal Obstruction 60 0.049
608
PRD004 Prediabetes Syndrome 49 0.049
609
ATN005 Autonomic Dysfunction 48 0.049
610
c JVN010 Juvenile Rheumatoid Arthritis 67 0.048
611
NRM005 Neuromuscular Disease 62 0.048
612
P HYP726 Hypercalcemia, Infantile, 1 58 0.048
613
TXC002 Toxic Encephalopathy 54 0.048
614
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.048
615
ASP007 Aspiration Pneumonia 46 0.048
616
P EPN002 Ependymoma 61 0.048
617
ERL001 Early Myoclonic Encephalopathy 60 0.048
618
P PLM034 Pulmonary Emphysema 55 0.048
619
P MYS005 Myositis 54 0.048
620
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.048
621
THR004 Thrombocytosis 52 0.048
622
RFR010 Refractory Anemia 50 0.048
623
DBT002 Diabetic Autonomic Neuropathy 45 0.048
624
RDN001 Reading Disorder 42 0.048
625
ESP002 Esophageal Varix 49 0.047
626
P GNG009 Gangliosidosis 45 0.047
627
TND005 Tendinitis 45 0.047
628
PPL001 Papillary Adenoma 42 0.047
629
PSR001 Psoriatic Arthritis 63 0.047
630
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.047
631
APP008 Appendicitis 61 0.047
632
P VNT002 Ventricular Septal Defect 61 0.047
633
BRN002 Bronchiolitis 60 0.047
634
P GLL020 Gallbladder Disease 60 0.047
635
FCT001 Factor Viii Deficiency 54 0.047
636
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.047
637
c BNG030 Benign Ependymoma 48 0.047
638
ACT084 Acute Stress Disorder 42 0.047
639
c OVR114 Ovarian Cancer 1 39 0.047
640
c HMP029 Hemophilia a 69 0.046
641
MYL031 Myeloproliferative Neoplasm 66 0.046
642
P OCL013 Oculodentodigital Dysplasia 65 0.046
643
P HMN010 Hemangioma 62 0.046
644
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.046
645
PST028 Post-Traumatic Stress Disorder 60 0.046
646
NWB001 Newborn Respiratory Distress Syndrome 58 0.046
647
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.046
648
PNM008 Pneumothorax 56 0.046
649
HRT011 Heart Septal Defect 52 0.046
650
MYL020 Myelomeningocele 51 0.046
651
LPT006 Leptin Receptor Deficiency 47 0.046
652
ASP008 Aspiration Pneumonitis 41 0.046
653
GNT003 Genital Herpes 54 0.046
654
P SYP003 Syphilis 59 0.046
655
P SJG008 Sjogren Syndrome 57 0.046
656
AMN001 Amenorrhea 54 0.046
657
IDP070 Idiopathic Scoliosis 39 0.046
658
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 34 0.046
659
CHK001 Chikungunya 55 0.046
660
RHM028 Rheumatic Heart Disease 54 0.046
661
MYL005 Myelofibrosis 69 0.046
662
KHL003 Kohlschutter-Tonz Syndrome 63 0.046
663
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.046
664
P CHR285 Chronic Myelomonocytic Leukemia 60 0.046
665
CLN045 Colonic Benign Neoplasm 52 0.046
666
VTM033 Vitamin K Deficiency Bleeding 47 0.046
667
HYP457 Hypertrophic Scars 44 0.046
668
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.046
669
BRS051 Breast Disease 59 0.045
670
P PRV006 Pervasive Developmental Disorder 58 0.045
671
ALC009 Alcoholic Liver Cirrhosis 53 0.045
672
HYP080 Hypogonadism 51 0.045
673
LMB062 Limb Ischemia 50 0.045
674
OVR063 Overnutrition 47 0.045
675
P RNL015 Renal Hypertension 47 0.045
676
P MCL001 Mucolipidosis 46 0.045
677
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.045
678
OBS002 Obsessive-Compulsive Disorder 69 0.045
679
PPL049 Papillon-Lefevre Syndrome 63 0.045
680
P MST009 Mastocytosis 62 0.045
681
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.045
682
P HMR003 Hemorrhagic Disease 54 0.045
683
LRN003 Learning Disability 51 0.045
684
RTN020 Retinal Vascular Disease 49 0.045
685
PRS063 Paresthesia 46 0.045
686
HYP064 Hypogonadotropism 40 0.045
687
CHL013 Cholecystolithiasis 37 0.045
688
MLC004 Mulchandani-Bhoj-Conlin Syndrome 31 0.045
689
PLY001 Polycythemia Vera 70 0.044
690
CRP001 Carpal Tunnel Syndrome 68 0.044
691
INC002 Inclusion Body Myositis 66 0.044
692
P ANR048 Aniridia 1 64 0.044
693
c GM1007 Gm1 Gangliosidosis 59 0.044
694
URN010 Urinary Tract Obstruction 59 0.044
695
P EPD016 Epidermolysis Bullosa 54 0.044
696
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.044
697
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.044
698
NNT012 Neonatal Jaundice 48 0.044
699
TTH006 Tooth Disease 47 0.044
700
RST023 Resting Heart Rate, Variation in 43 0.044
701
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.044
702
P DRM010 Dermatomyositis 62 0.044
703
P BRN022 Bronchiectasis 60 0.044
704
HRP004 Herpes Zoster 58 0.044
705
ACD008 Acid-Labile Subunit Deficiency 55 0.044
706
CRN017 Coronary Thrombosis 45 0.044
707
GNG003 Gingival Recession 43 0.044
708
TRP009 Triple X Syndrome 42 0.044
709
c PLY105 Polycystic Ovary Syndrome 1 38 0.044
710
PMP006 Pemphigus Vulgaris, Familial 56 0.044
711
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.043
712
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.043
713
END041 Endometrial Adenocarcinoma 64 0.043
714
APN008 Apnea, Obstructive Sleep 64 0.043
715
BRS099 Breast Ductal Carcinoma 63 0.043
716
BRC012 Brucellosis 62 0.043
717
c DNG003 Dengue Disease 61 0.043
718
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.043
719
CMR002 Coumarin Resistance 56 0.043
720
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.043
721
c MLG079 Malignant Pleural Mesothelioma 43 0.043
722
c SYS043 Systemic Lupus Erythematosus 1 39 0.043
723
P APL001 Aplastic Anemia 76 0.043
724
CRT072 Creutzfeldt-Jakob Disease 67 0.043
725
c ALP101 Alpha-Thalassemia 63 0.043
726
INT066 Interstitial Lung Disease 61 0.043
727
c HRD002 Hereditary Angioedema 59 0.043
728
ERY003 Erythema Multiforme 57 0.043
729
P NRV006 Nervous System Cancer 55 0.043
730
CLN019 Colonic Disease 55 0.043
731
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.043
732
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.043
733
P RTT002 Rett Syndrome 81 0.042
734
c WLM013 Wilms Tumor 1 69 0.042
735
P CHR012 Chronic Granulomatous Disease 69 0.042
736
HMR039 Hemorrhage, Intracerebral 59 0.042
737
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.042
738
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.042
739
P HYP733 Hypercalciuria, Absorptive, 2 45 0.042
740
ACT088 Acute Insulin Response 42 0.042
741
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.042
742
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.042
743
P BLD062 Bile Duct Cancer 66 0.042
744
c MCL013 Mucolipidosis Iv 60 0.042
745
PLS007 Plasmodium Falciparum Malaria 53 0.042
746
INF034 Infective Endocarditis 53 0.042
747
GNT002 Giant Cell Glioblastoma 52 0.042
748
c CNT033 Central Nervous System Cancer 51 0.042
749
DGN001 Degenerative Disc Disease 49 0.042
750
CRB090 Cerebral Hypoxia 45 0.042
751
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.042
752
GLC008 Glucose Metabolism Disease 47 0.042
753
c TBR025 Tuberous Sclerosis 1 74 0.042
754
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.042
755
P DBT005 Diabetes Insipidus 54 0.042
757
CYN002 Cyanosis, Transient Neonatal 45 0.042
758
P DYS005 Dyslexia 42 0.042
759
ADS004 Aids Dementia Complex 41 0.042
760
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.041
761
SVR097 Severe Cutaneous Adverse Reaction 66 0.041
762
HRT012 Heart Valve Disease 56 0.041
763
CLF004 Cleft Lip/palate 55 0.041
764
c XNT010 Xanthinuria, Type I 51 0.041
765
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.041
766
PRM020 Premenstrual Tension 48 0.041
767
FSC004 Fasciitis 47 0.041
768
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.041
769
TND004 Tendinopathy 44 0.041
770
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.041
771
ATM052 Autoimmune Disease 1 38 0.041
772
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 37 0.041
773
SPN027 Spinal Stenosis 58 0.041
774
P ANT006 Antiphospholipid Syndrome 56 0.041
775
DCB001 Decubitus Ulcer 54 0.041
776
HMG002 Hemoglobinuria 49 0.041
777
TST014 Testicular Cancer 49 0.041
778
BLP005 Blepharitis 48 0.041
779
GRW007 Growth Hormone Deficiency 48 0.041
780
BNM001 Bone Marrow Cancer 48 0.041
781
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.041
782
ERY066 Erythema Multiforme Major 29 0.041
783
P PLY041 Polymyositis 57 0.040
784
ORL005 Oral Candidiasis 56 0.040
785
P ESP035 Esophagitis, Eosinophilic, 1 54 0.040
786
GST037 Gastroparesis 52 0.040
787
CRD137 Cardiogenic Shock 50 0.040
788
SKN013 Skin Benign Neoplasm 49 0.040
789
LWC001 Low Compliance Bladder 45 0.040
790
GST020 Gastric Antral Vascular Ectasia 42 0.040
791
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 37 0.040
792
CYT018 Cytochrome P450 2d6 Variant 28 0.040
793
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.040
794
HDG004 Hodgkin's Granuloma 27 0.040
795
HDG006 Hodgkin's Paragranuloma 23 0.040
796
P PLV020 Pelvic Organ Prolapse 61 0.040
797
c PNC108 Pancreatitis, Hereditary 70 0.039
798
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.039
799
GLL008 Gilles De La Tourette Syndrome 66 0.039
800
KWS002 Kawasaki Disease 65 0.039
801
ART002 Arts Syndrome 63 0.039
802
BLL006 Bullous Pemphigoid 63 0.039
803
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.039
804
ING001 Inguinal Hernia 61 0.039
805
P MLG056 Malignant Hyperthermia 60 0.039
806
LMY014 Leiomyoma, Uterine 57 0.039
807
P TCD001 Tic Disorder 55 0.039
808
OCL006 Ocular Hypertension 52 0.039
809
ANG005 Anogenital Venereal Wart 51 0.039
810
ACR041 Acromelic Frontonasal Dysostosis 50 0.039
811
CRT013 Carotid Stenosis 50 0.039
812
ORL013 Oral Lichen Planus 47 0.039
813
HRN029 Hearing Loss, Noise-Induced 38 0.039
814
c ACT004 Acute Diarrhea 38 0.039
815
FRN006 Frontotemporal Dementia 70 0.039
816
P TYS001 Tay-Sachs Disease 68 0.039
817
NRL005 Neurilemmoma 62 0.039
818
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.039
819
P STR020 Strabismus 57 0.039
820
HMP005 Hemiplegia 55 0.039
821
c LKM070 Leukemia, Acute Monocytic 55 0.039
822
P HYP040 Hypospadias 54 0.039
823
RNL011 Renal Osteodystrophy 49 0.039
824
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.039
825
OLG001 Oligospermia 44 0.039
826
MCH006 Mechanical Strabismus 31 0.039
827
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.038
828
CMP010 Complex Regional Pain Syndrome 57 0.038
829
APH001 Aphthous Stomatitis 56 0.038
830
NRG002 Neurogenic Bladder 55 0.038
831
MCN017 Meconium Ileus 54 0.038
832
STP011 Stapes Ankylosis with Broad Thumbs and Toes 50 0.038
833
P OVR046 Ovarian Cyst 50 0.038
834
c BPL002 Bipolar I Disorder 48 0.038
835
CCN002 Cocaine Abuse 48 0.038
836
P SCL057 Scoliosis, Isolated 1 41 0.038
837
HMR023 Hemorrhagic Cystitis 40 0.038
838
HML018 Homologous Wasting Disease 22 0.038
839
c ART101 Aortic Valve Disease 2 67 0.038
840
TBC004 Tobacco Addiction 65 0.038
841
NRF007 Neurofibroma 63 0.038
842
HSH003 Hashimoto Thyroiditis 63 0.038
843
P LMY004 Leiomyosarcoma 63 0.038
844
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.038
845
c LCL006 Localized Scleroderma 61 0.038
846
ALV005 Alveolar Soft Part Sarcoma 56 0.038
847
c CHR418 Chronic Leukemia 52 0.038
848
P THR015 Thrombophilia 51 0.038
849
P LCT002 Lactose Intolerance 51 0.038
850
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.038
851
SXL003 Sexual Disorder 49 0.038
852
P BLD051 Blood Coagulation Disease 48 0.038
853
MYF001 Myofibroma 40 0.038
854
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.038
855
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.037
856
PCK003 Pick Disease of Brain 63 0.037
857
P MMB011 Membranous Nephropathy 54 0.037
858
P RST001 Restless Legs Syndrome 54 0.037
859
P BRN035 Brain Stem Glioma 51 0.037
860
P ANL018 Analbuminemia 51 0.037
861
ACH005 Achalasia 50 0.037
862
STM006 Stomach Disease 50 0.037
863
TRC008 Trachoma 49 0.037
864
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.037
865
c BSL024 Basal Cell Carcinoma 1 47 0.037
866
HMR002 Hemarthrosis 46 0.037
867
GLY031 Glycoproteinosis 45 0.037
868
KHN001 Kuhnt-Junius Degeneration 45 0.037
869
P PRL003 Proliferative Glomerulonephritis 43 0.037
870
P ESS003 Essential Thrombocythemia 69 0.037
871
P ATR010 Atrial Heart Septal Defect 61 0.037
872
PRT058 Pure Autonomic Failure 60 0.037
873
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.037
874
GNR004 Generalized Anxiety Disorder 55 0.037
875
FRZ001 Frozen Shoulder 53 0.037
876
OPT003 Opiate Dependence 50 0.037
877
SYN036 Syncope 46 0.037
878
c DRM054 Dermatitis, Atopic, 2 45 0.037
879
MYF002 Myofascial Pain Syndrome 39 0.037
880
CWM001 Cow Milk Allergy 37 0.037
881
PSD088 Pseudobulbar Affect 37 0.037
882
ASC010 Ascaris Lumbricoides Infection 51 0.036
883
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.036
884
P KRB001 Krabbe Disease 68 0.036
885
FBR012 Fabry Disease 68 0.036
886
P PTN014 Patent Ductus Arteriosus 1 60 0.036
887
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.036
888
ATR057 Atrioventricular Block 56 0.036
889
ORL004 Oral Submucous Fibrosis 55 0.036
890
P KRT007 Keratoconus 51 0.036
891
PRV004 Periventricular Leukomalacia 50 0.036
892
P MGR001 Migraine Without Aura 47 0.036
893
DRG024 Drug Allergy 43 0.036
894
MND023 Mend Syndrome 42 0.036
895
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.036
896
MCP033 Mucopolysaccharidoses 39 0.036
897
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.036
898
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.036
899
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.036
900
PRX034 Peroxisome Disorders 22 0.036
901
P PRM011 Primary Ciliary Dyskinesia 67 0.036
902
P MTC003 Metachromatic Leukodystrophy 69 0.035
903
DNG002 Dengue Hemorrhagic Fever 59 0.035
904
c ANG068 Angioedema, Hereditary, Type I 57 0.035
905
c CHR417 Chronic Graft Versus Host Disease 56 0.035
906
P VNS003 Venous Insufficiency 55 0.035
907
CYS005 Cysticercosis 55 0.035
908
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.035
909
RDC002 Radiculopathy 51 0.035
910
RFL001 Reflex Sympathetic Dystrophy 50 0.035
911
MLL001 Molluscum Contagiosum 49 0.035
912
CLC006 Calcinosis 48 0.035
913
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.035
914
AVD001 Avoidant Personality Disorder 45 0.035
915
SPN050 Spinocerebellar Degeneration 43 0.035
916
ANG049 Angioedema Induced by Ace Inhibitors 41 0.035
917
SCR015 Scarlet Fever 41 0.035
918
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.035
919
ASC001 Ascaridiasis 36 0.035
920
c NRF024 Neurofibromatosis, Type I 72 0.035
921
P MTR004 Maturity-Onset Diabetes of the Young 66 0.035
922
PNM010 Pneumothorax, Primary Spontaneous 60 0.035
923
SPS003 Spastic Diplegia 53 0.035
924
QDR001 Quadriplegia 51 0.035
925
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.035
926
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 48 0.035
927
BHR001 Behr Syndrome 47 0.035
928
DFF003 Diffuse Scleroderma 43 0.035
929
SYS003 Systolic Heart Failure 43 0.035
930
P HYP263 Hypersomnia 42 0.035
931
ALG001 Algoneurodystrophy 38 0.035
932
P TTR001 Tetralogy of Fallot 70 0.034
933
CMM004 Common Variable Immunodeficiency 69 0.034
934
P ANP001 Anaplastic Large Cell Lymphoma 62 0.034
935
TNG003 Tongue Cancer 57 0.034
936
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.034
937
APH002 Aphasia 56 0.034
938
BLM002 Bulimia Nervosa 56 0.034
939
HRL003 Hurler Syndrome 55 0.034
940
P HYP083 Hypopituitarism 53 0.034
941
HMT008 Hematuria, Benign Familial 53 0.034
942
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.034
943
BRN038 Bronchial Disease 53 0.034
944
IMM136 Immune System Disease 52 0.034
945
CYS014 Cystadenocarcinoma 51 0.034
946
APR001 Apraxia 50 0.034
947
BLD044 Bladder Disease 50 0.034
948
CCN001 Cocaine Dependence 48 0.034
949
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 47 0.034
950
ANP009 Anaplastic Oligodendroglioma 44 0.034
951
PRL008 Paralytic Ileus 43 0.034
952
FTL021 Fetal Macrosomia 43 0.034
953
BRS064 Bursitis 42 0.034
954
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.034
955
CLS047 Classic Progressive Supranuclear Palsy Syndrome 30 0.034
956
AGM019 Agammaglobulinemia, X-Linked 71 0.033
957
P AGM001 Agammaglobulinemia 66 0.033
958
MGK001 Megakaryocytic Leukemia 65 0.033
959
INT146 Intervertebral Disc Disease 64 0.033
960
P MCH002 Machado-Joseph Disease 61 0.033
961
c PRM012 Primary Polycythemia 52 0.033
962
CHR005 Chorioamnionitis 51 0.033
963
HYP063 Hypersplenism 51 0.033
964
c PRM226 Primary Central Nervous System Lymphoma 50 0.033
965
SPH010 Sphingolipidosis 47 0.033
966
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.033
967
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.033
968
IDP033 Idiopathic Edema 44 0.033
969
HRD005 Hard Palate Cancer 41 0.033
970
HYP264 Hypertonia 39 0.033
971
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.033
972
RSP007 Respiratory Distress Syndrome, Infant 31 0.033
973
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.033
974
SMT004 Smith-Lemli-Opitz Syndrome 67 0.033
975
FLL027 Fallopian Tube Carcinoma 64 0.033
976
RSP006 Respiratory System Disease 57 0.033
977
ASP002 Aspartylglucosaminuria 55 0.033
978
PLY023 Polycystic Liver Disease 55 0.033
979
P IGN003 Iga Nephropathy 1 50 0.033
980
P ASP001 Asperger Syndrome 48 0.033
981
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.033
982
SMT001 Somatization Disorder 45 0.033
983
ENT001 Enterocele 44 0.033
984
APP009 Appendix Adenocarcinoma 43 0.033
985
PST053 Postherpetic Neuralgia 43 0.033
986
P CRN024 Corneal Disease 42 0.033
987
ACL001 Acalculous Cholecystitis 35 0.033
988
TTH004 Tethered Spinal Cord Syndrome 33 0.033
989
PGM030 Pigmentation Anomaly of the Skin 26 0.033
990
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 65 0.032
991
SML019 Smallpox 55 0.032
992
P MGR003 Migraine with Aura 53 0.032
993
URN009 Urinary System Disease 52 0.032
994
SRS001 Serous Cystadenocarcinoma 51 0.032
995
c BRS049 Breast Carcinoma in Situ 51 0.032
996
CLR003 Clear Cell Adenocarcinoma 51 0.032
997
P END047 Endophthalmitis 50 0.032
998
ISL003 Isolated Growth Hormone Deficiency 50 0.032
999
MCN001 Mucinous Adenocarcinoma 50 0.032
1000
SPC010 Speech and Communication Disorders 46 0.032
1001
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.032
1002
PRL017 Prolymphocytic Leukemia 45 0.032
1003
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.032
1004
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.032
1005
CLL014 Cll/sll 44 0.032
1006
P RRT020 Rare Tumor 43 0.032
1007
CNN001 Cannabis Dependence 41 0.032
1008
CNN002 Cannabis Abuse 40 0.032
1009
SWL001 Swallowing Disorders 39 0.032
1010
OLG006 Oligoastrocytoma 36 0.032
1011
c MYS011 Myasthenia Gravis Congenital 31 0.032
1012
TMP019 Temporomandibular Joint Anomaly 29 0.032
1013
MLD010 Mild Phenylketonuria 29 0.032
1014
MSM014 Mismatch Repair Cancer Syndrome 65 0.031
1015
P ART005 Arteriovenous Malformation 63 0.031
1016
c GM1004 Gm1-Gangliosidosis, Type I 58 0.031
1017
AND020 Androgen Insensitivity, Partial 56 0.031
1018
GRN034 Grange Syndrome 55 0.031
1019
P URF003 Urofacial Syndrome 1 55 0.031
1020
P OVR049 Ovarian Disease 55 0.031
1021
PRL032 Perlman Syndrome 54 0.031
1022
P CNT005 Central Nervous System Lymphoma 52 0.031
1023
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.031
1024
GLM004 Gliomatosis Cerebri 50 0.031
1025
P IDP024 Idiopathic Inflammatory Myopathy 49 0.031
1026
HYL004 Hyaline Fibromatosis Syndrome 49 0.031
1027
VRL003 Variola Major 48 0.031
1028
c PRM093 Premature Ovarian Failure 7 48 0.031
1029
CRB008 Cerebral Atherosclerosis 47 0.031
1030
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 45 0.031
1031
P OCY003 Oocyte Maturation Defect 1 44 0.031
1032
MCL003 Macular Holes 44 0.031
1033
PLY068 Polysubstance Abuse 44 0.031
1034
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.031
1035
c SRC023 Sarcoidosis 2 43 0.031
1036
STL007 Steel Syndrome 42 0.031
1037
PLS016 Plasma Cell Leukemia 41 0.031
1038
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.031
1039
THR017 Thoracoabdominal Syndrome 38 0.031
1040
ORB013 Orbital Disease 38 0.031
1041
c WLM011 Wilms Tumor 6 38 0.031
1042
SCR003 Secretory Diarrhea 36 0.031
1043
CYT004 Cytomegalic Inclusion Disease 32 0.031
1044
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.030
1045
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.030
1046
c MCP049 Mucopolysaccharidosis, Type Vii 60 0.030
1047
EXT034 Extrinsic Allergic Alveolitis 58 0.030
1048
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 58 0.030
1049
LNN001 Lennox-Gastaut Syndrome 56 0.030
1050
c ADL096 Adult Hepatocellular Carcinoma 56 0.030
1051
PST046 Post-Transplant Lymphoproliferative Disease 55 0.030
1052
P HYP730 Hypogonadotropic Hypogonadism 54 0.030
1053
P SPN052 Spondyloarthropathy 54 0.030
1054
FCL012 Facial Paralysis 53 0.030
1055
CRB150 Cerebral Creatine Deficiency Syndrome 2 52 0.030
1056
OPD006 Opioid Addiction 49 0.030
1057
SCL003 Social Phobia 49 0.030
1058
PCT003 Pectus Excavatum 48 0.030
1059
c CHR431 Chronic Venous Insufficiency 48 0.030
1060
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.030
1061
c THR090 Thrombocythemia 1 47 0.030
1062
LCK001 Locked-in Syndrome 46 0.030
1063
AYM001 Ayme-Gripp Syndrome 45 0.030
1064
P CMP008 Compartment Syndrome 45 0.030
1065
c DYS119 Dystonia 9 45 0.030
1066
ADN001 Adenosine Deaminase Deficiency 44 0.030
1067
c ADL008 Adult Oligodendroglioma 40 0.030
1068
C1N001 C1 Inhibitor Deficiency 39 0.030
1069
c RST012 Restless Legs Syndrome 1 34 0.030
1070
P OVR096 Overlap Myositis 28 0.030
1071
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.030
1072
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.030
1073
TKY002 Takayasu Arteritis 61 0.030
1074
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 59 0.030
1075
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.030
1076
P PSD015 Pseudohypoparathyroidism 54 0.030
1077