Search results for hydroxyproline

961 hits were found for hydroxyproline

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 48 6.601
2
BNR002 Bone Resorption Disease 47 6.456
3
P PLM036 Pulmonary Fibrosis 65 4.909
4
P BND020 Bone Disease 60 4.500
5
P HYP069 Hyperparathyroidism 62 4.382
6
P PRM002 Primary Hyperoxaluria 65 4.375
7
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 4.008
8
HLX001 Helix Syndrome 47 3.969
9
MMM001 Mammary Paget's Disease 53 3.871
10
HYD031 Hydroxyprolinemia 19 3.410
11
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.394
12
P OST002 Osteoporosis 76 3.394
13
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.394
14
c PRM005 Primary Hyperparathyroidism 59 3.361
15
IMN001 Iminoglycinuria 41 3.117
16
P HYP076 Hyperthyroidism 53 2.849
17
OST011 Osteomalacia 52 2.755
18
SLC006 Silicosis 55 2.692
19
P PGT001 Paget's Disease of Bone 60 2.677
20
RCK004 Rickets 64 2.446
21
URM002 Uremia 47 2.058
22
c SCN007 Secondary Hyperparathyroidism 50 2.032
23
c SCL052 Scleroderma, Familial Progressive 60 2.010
24
P SYS005 Systemic Scleroderma 73 2.010
25
P ART023 Arthropathy 59 1.978
26
RNL011 Renal Osteodystrophy 48 1.875
27
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.842
28
BRT054 Brittle Bone Disorder 74 1.792
29
P SCL018 Scoliosis 57 1.686
30
HYP348 Hyperglycinuria 38 1.660
31
c VRL010 Viral Hepatitis 52 1.620
32
ANT018 Anthracosis 50 1.612
33
LVR012 Liver Cirrhosis 62 1.610
34
P MSC005 Muscular Dystrophy 66 1.610
35
P PNM006 Pneumoconiosis 55 1.603
36
48X005 48,xyyy 39 1.594
37
P KDN018 Kidney Disease 71 1.585
38
PRL019 Prolidase Deficiency 50 1.582
39
BRN024 Bronchitis 67 1.557
40
HYP781 Hypoascorbemia 52 1.537
41
P SRC025 Sarcoidosis 1 70 1.533
42
ACR007 Acromegaly 70 1.513
43
P ART021 Arteriosclerosis 53 1.491
44
P GLM007 Glomerulonephritis 59 1.484
45
LTH004 Lathyrism 15 1.475
46
NPH009 Nephrolithiasis 54 1.463
47
PRS045 Prostatic Hypertrophy 53 1.449
48
c GRV008 Graves Disease 1 54 1.436
49
P HYP086 Hypothyroidism 68 1.425
50
P HYP024 Hypoparathyroidism 55 1.396
51
P HYP111 Hyperprolinemia 44 1.396
52
FBR009 Fibrous Dysplasia 48 1.386
53
CLT003 Colitis 63 1.376
54
P NPH012 Nephrotic Syndrome 61 1.354
55
MYL005 Myelofibrosis 70 1.343
56
ADN018 Adenoma 58 1.333
57
MYL069 Myeloma, Multiple 76 1.307
58
PRT029 Parathyroid Adenoma 51 1.295
59
BNN003 Bone Inflammation Disease 47 1.294
60
c SPN225 Spondyloarthropathy 1 70 1.269
61
SPN051 Spondylitis 51 1.269
62
INF009 Inflammatory Spondylopathy 30 1.269
63
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.258
64
SKN016 Skin Disease 63 1.258
65
NNL006 Non-Alcoholic Steatohepatitis 54 1.245
66
OST012 Osteoarthritis 77 1.245
67
CNN005 Connective Tissue Disease 66 1.228
68
PLM001 Pulmonary Tuberculosis 69 1.225
69
URT010 Ureteral Obstruction 44 1.224
70
HYP266 Hypoxia 56 1.196
71
IDP070 Idiopathic Scoliosis 41 1.174
72
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 1.174
73
P TMR010 Tumor Predisposition Syndrome 69 1.174
74
PST011 Pustulosis of Palm and Sole 52 1.174
75
P PSR002 Psoriasis 63 1.174
76
INH023 Inherited Cancer-Predisposing Syndrome 53 1.174
77
GTR002 Goiter 52 1.164
78
P PLM037 Pulmonary Hypertension 69 1.158
79
P LVR013 Liver Disease 68 1.143
80
OST016 Osteochondrosis 52 1.134
81
P FBR017 Fibrosarcoma 55 1.114
82
AGN016 Aging 53 1.110
83
HYP457 Hypertrophic Scars 42 1.102
84
c MCR133 Microvascular Complications of Diabetes 4 41 1.102
85
c MCR113 Microvascular Complications of Diabetes 3 52 1.102
86
c MCR130 Microvascular Complications of Diabetes 6 41 1.102
87
c MCR120 Microvascular Complications of Diabetes 7 47 1.102
88
OST159 Osteogenic Sarcoma 66 1.093
89
FML345 Familial Expansile Osteolysis 46 1.092
90
P HPT023 Hepatocellular Carcinoma 95 1.087
91
LNG099 Lung Disease 62 1.084
92
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.073
93
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.073
94
c HYP603 Hyperoxaluria, Primary, Type Iii 50 1.073
95
P TBR001 Tuberous Sclerosis 69 1.073
96
P PRD008 Periodontitis 63 1.073
97
P EHL001 Ehlers-Danlos Syndrome 57 1.058
98
P PNC035 Pancreatic Cancer 87 1.057
99
c MCR115 Microvascular Complications of Diabetes 5 65 1.057
100
c BRC048 Bruck Syndrome 2 32 1.034
101
NPH003 Nephrocalcinosis 49 1.024
102
THY030 Thyroid Gland Disease 50 1.012
103
c HYP836 Hypercholesterolemia, Familial, 1 73 1.000
104
P MYP006 Myopia 55 0.989
105
P ANP001 Anaplastic Large Cell Lymphoma 59 0.987
106
ASB001 Asbestosis 47 0.979
107
ASB003 Asbestos Intoxication 32 0.979
108
c TYP008 Type 1 Diabetes Mellitus 77 0.968
109
OST004 Osteitis Fibrosa 38 0.968
110
INT067 Interstitial Nephritis 46 0.966
111
BRS051 Breast Disease 58 0.966
112
P CLL015 Collagen Disease 47 0.966
113
GLM044 Glomerular Disease 34 0.966
114
c ACT027 Acute Pancreatitis 60 0.957
115
HYP052 Hyperkalemic Periodic Paralysis 62 0.943
116
c HYP794 Hyperoxaluria, Primary, Type I 63 0.943
117
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.943
118
c HYP597 Hyperprolinemia, Type Ii 43 0.943
119
OST003 Osteonecrosis 60 0.943
120
P VTR007 Vitreoretinopathy 45 0.943
121
ING001 Inguinal Hernia 59 0.934
122
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.934
123
47X002 47,xyy 47 0.934
124
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.909
125
P KRT007 Keratoconus 49 0.909
126
BRN056 Bronchopulmonary Dysplasia 57 0.909
127
RNL077 Renal Fibrosis 46 0.903
128
P OPN001 Open-Angle Glaucoma 55 0.896
129
ICH077 Ichthyosis, Split Hairs, and Amino Aciduria 8 0.895
130
P AMY004 Amyloidosis 69 0.885
131
GRW007 Growth Hormone Deficiency 47 0.885
132
DWR001 Dwarfism 44 0.885
133
URL001 Urolithiasis 45 0.883
134
P DBT009 Diabetes Mellitus 67 0.883
135
INS024 Insulin-Like Growth Factor I 77 0.881
136
P INF037 Inflammatory Bowel Disease 53 0.869
137
GST023 Gastric Ulcer 52 0.869
138
ENT004 Enthesopathy 51 0.869
139
ALC006 Alcoholic Hepatitis 61 0.869
140
ATS010 Autosomal Recessive Disease 42 0.854
141
P OST001 Osteopetrosis 70 0.854
142
P INT070 Intestinal Obstruction 57 0.854
143
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.842
144
MTB004 Metabolic Acidosis 48 0.839
145
CYS001 Cystic Fibrosis 77 0.839
146
PCT003 Pectus Excavatum 43 0.839
147
c HYP311 Hyperparathyroidism 3 17 0.839
148
P HYP730 Hypogonadotropic Hypogonadism 57 0.839
149
PRP016 Paraplegia 52 0.839
150
ABD010 Abdominal Wall Defect 37 0.839
151
ATH013 Atherosclerosis Susceptibility 63 0.823
152
P MPL001 Maple Syrup Urine Disease 69 0.823
153
P GRF003 Graft-Versus-Host Disease 71 0.823
154
PYR009 Pyridoxine Deficiency Anemia 35 0.823
155
c HPT073 Hepatitis C Virus 70 0.806
156
CHL065 Cholangiocarcinoma 57 0.806
157
INT079 Intrahepatic Cholangiocarcinoma 51 0.806
158
AMN006 Aminoaciduria 37 0.806
159
PRT036 Peritonitis 65 0.801
160
CHL068 Cholestasis 61 0.794
161
RTN017 Retinal Detachment 60 0.788
162
P MCR129 Microvascular Complications of Diabetes 1 67 0.788
163
c MCR112 Microvascular Complications of Diabetes 2 42 0.788
164
P HYP750 Hypertriglyceridemia, Familial 61 0.788
165
P LPR021 Leprosy 3 71 0.788
166
PHN003 Phenylketonuria 76 0.788
168
HYP060 Hyperinsulinism 53 0.788
169
SYN007 Synovitis 54 0.788
170
PLC002 Plica Syndrome 35 0.788
171
LMY002 Leiomyoma 51 0.788
172
HNS001 Hansen's Disease 32 0.788
173
P SCK005 Sickle Cell Disease 56 0.788
174
c SYS001 Systemic Lupus Erythematosus 85 0.769
175
PNM010 Pneumothorax, Primary Spontaneous 58 0.769
176
INT051 Intussusception 53 0.769
177
OST017 Osteomyelitis 63 0.769
178
PNM008 Pneumothorax 54 0.769
179
c HPT001 Hepatitis C 61 0.769
180
ALC009 Alcoholic Liver Cirrhosis 54 0.769
181
APP008 Appendicitis 62 0.769
182
P OVR082 Overgrowth Syndrome 41 0.769
183
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.757
184
SCH014 Schistosomiasis 56 0.757
185
c GLC092 Glaucoma, Primary Open Angle 60 0.748
186
P ORT004 Orthostatic Intolerance 61 0.748
187
P PRP029 Porphyria 60 0.748
188
TBL003 Tubular Adenocarcinoma 40 0.748
189
c ACT073 Acute Leukemia 59 0.748
190
HYD005 Hydrocele 46 0.748
191
ANG054 Angina Pectoris 65 0.746
192
PRT013 Portal Hypertension 59 0.731
193
c PRD040 Periodontitis, Chronic 52 0.724
194
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.724
195
LMY014 Leiomyoma, Uterine 55 0.724
196
P PLY014 Polycystic Kidney Disease 71 0.724
197
P BRS053 Breast Fibroadenoma 48 0.724
198
HYD003 Hydrarthrosis 33 0.724
199
GT001 Gout 63 0.724
200
P MYT002 Myotonic Dystrophy 51 0.724
201
STN013 Stenotrophomonas Maltophilia Infection 26 0.724
202
ALL003 Allergic Rhinitis 66 0.698
203
P OVR042 Ovarian Cancer 88 0.698
204
P PRP003 Porphyria Cutanea Tarda 66 0.698
205
HYP611 Hypoparathyroidism, X-Linked 29 0.698
206
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.698
207
c EXS021 Exostoses, Multiple, Type Iii 19 0.698
208
OPS001 Opisthorchiasis 41 0.698
209
P HPT021 Hepatitis 68 0.698
210
GST045 Gastroenteritis 58 0.698
211
IRN002 Iron Metabolism Disease 56 0.698
212
P PLY019 Polyneuropathy 52 0.698
213
P KDN017 Kidney Cancer 60 0.698
214
P RHN004 Rhinitis 56 0.698
215
PNT038 Peanut Allergy 45 0.698
216
GNG012 Gingival Overgrowth 49 0.698
217
TNS005 Tonsillitis 57 0.698
218
DNT010 Dentin Caries 32 0.698
219
c PRC016 Pre-Eclampsia 64 0.698
220
PRC013 Pericarditis 53 0.698
221
ACQ007 Acquired Immunodeficiency Syndrome 58 0.698
222
MCL003 Macular Holes 44 0.698
223
BCK006 Back Pain 43 0.698
224
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.690
225
FTT001 Fatty Liver Disease 61 0.668
226
PSR001 Psoriatic Arthritis 61 0.667
227
P DRM053 Dermatitis, Atopic 65 0.667
228
ANR007 Anorexia Nervosa 59 0.667
229
ASP002 Aspartylglucosaminuria 57 0.667
230
P ALP004 Alport Syndrome 69 0.667
231
MYF001 Myofibroma 42 0.667
232
BLL003 Bell's Palsy 48 0.667
233
c SBC010 Subacute Glomerulonephritis 23 0.667
234
CHG001 Chagas Disease 65 0.667
235
LNG031 Lung Benign Neoplasm 51 0.667
236
P HYP083 Hypopituitarism 51 0.667
237
P THL005 Thalassemia 56 0.667
238
PLY100 Polyploidy 36 0.667
239
P PNC044 Pancreatitis 61 0.639
240
NRL016 Neural Tube Defects 80 0.626
241
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.626
242
KSH004 Kashin-Beck Disease 37 0.626
243
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.626
244
VCC001 Vaccinia 49 0.626
245
KWS001 Kwashiorkor 44 0.626
246
HMP001 Hemopericardium 47 0.626
247
PLM012 Pulmonary Sarcoidosis 52 0.626
248
P EYD002 Eye Disease 57 0.626
249
P URN019 Urinary Tract Infection 48 0.626
250
BRC012 Brucellosis 66 0.626
251
P GST044 Gastritis 55 0.626
252
P PRC012 Pericardial Effusion 50 0.626
253
PMP014 Pemphigoid 48 0.626
254
P CTR002 Cataract 59 0.626
255
BLL006 Bullous Pemphigoid 61 0.626
256
P PMP001 Pemphigus 54 0.626
257
SNL007 Senile Cataract 40 0.626
258
P TXP001 Toxoplasmosis 59 0.626
259
SCL025 Scleromyxedema 37 0.626
260
CNG587 Congenital Limb Malformation 12 0.626
261
KLD004 Keloid Disorder 38 0.599
262
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.527
263
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.527
264
RTN020 Retinal Vascular Disease 45 0.527
265
GST071 Gastrointestinal Carcinoma 46 0.527
266
ART008 Arteriosclerosis Obliterans 40 0.527
267
RTR008 Root Resorption 44 0.527
268
GST049 Gastrointestinal System Cancer 49 0.527
269
GST010 Gestational Trophoblastic Neoplasm 52 0.527
270
DBT008 Diabetic Angiopathy 47 0.527
271
TRP004 Tropical Sprue 39 0.527
272
P UVT001 Uveitis 57 0.527
273
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.521
274
CYT002 Cytokine Deficiency 43 0.521
275
INT066 Interstitial Lung Disease 60 0.512
276
HYP066 Hyperglycemia 60 0.502
277
PLM010 Pulmonary Edema 54 0.502
278
MSC157 Muscular Dystrophy, Duchenne Type 78 0.483
279
HMS001 Hemosiderosis 48 0.483
280
P RRH023 Rare Hereditary Hemochromatosis 52 0.483
281
CHR100 Chronic Ulcer of Skin 57 0.462
282
HYP017 Hypophosphatemia 49 0.462
283
P MYC007 Myocardial Infarction 69 0.462
284
P CHL066 Cholangitis 51 0.462
285
IDP073 Idiopathic Hypercalciuria 41 0.462
286
PRT251 Proteinuria, Chronic Benign 58 0.441
287
PPL052 Papillomatosis, Confluent and Reticulated 34 0.441
288
P ADL010 Adult Respiratory Distress Syndrome 70 0.430
289
EXT034 Extrinsic Allergic Alveolitis 56 0.430
290
c ATR087 Atrial Standstill 1 74 0.418
291
ART016 Aortic Aneurysm 68 0.418
292
c TYP009 Type 2 Diabetes Mellitus 91 0.406
293
HYP080 Hypogonadism 49 0.406
294
TND005 Tendinitis 53 0.394
295
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.394
296
SVR004 Severe Combined Immunodeficiency 70 0.394
297
c DLT002 Dilated Cardiomyopathy 79 0.394
298
P MYC008 Myocarditis 59 0.394
299
c CHR711 Chronic Asthma 41 0.382
300
P SCL009 Sclerosing Cholangitis 46 0.382
301
P OBS001 Obstructive Jaundice 49 0.382
302
P RNL015 Renal Hypertension 45 0.382
303
PRQ002 Paraquat Poisoning 28 0.382
304
SPL018 Splenomegaly 47 0.382
305
SPN186 Spinal Cord Injury 60 0.382
306
IMP005 Impotence 52 0.369
307
ISC004 Ischemia 61 0.369
308
CNG034 Congestive Heart Failure 69 0.369
309
P HRT032 Heart Disease 84 0.369
310
PRM236 Primary Biliary Cholangitis 62 0.369
311
DGN001 Degenerative Disc Disease 48 0.369
312
P BCL017 B-Cell Lymphoma 57 0.369
313
c CHR684 Chronic Kidney Disease 73 0.369
314
P RSP003 Respiratory Failure 73 0.355
315
P END044 Endometriosis 62 0.355
316
PRT038 Protein-Energy Malnutrition 53 0.355
317
ANR040 Aneurysm 60 0.355
318
PYR010 Peyronie's Disease 50 0.341
319
MRF001 Marfan Syndrome 76 0.341
320
P RNV001 Renovascular Hypertension 48 0.341
321
P ESP024 Esophagitis 60 0.341
322
ALL029 Allergic Disease 61 0.341
323
c CHL119 Cholangitis, Primary Sclerosing 57 0.327
324
RTC003 Root Caries 33 0.327
325
c FML015 Familial Nephrotic Syndrome 48 0.327
326
P ART022 Arthritis 70 0.327
327
ALL006 Allergic Asthma 55 0.327
328
CRH001 Crohn's Disease 80 0.327
329
P HYP098 Hypereosinophilic Syndrome 66 0.327
330
VRC005 Varicose Veins 59 0.312
331
INT017 Intestinal Schistosomiasis 51 0.312
332
c PGT008 Paget Disease of Bone 5, Juvenile-Onset 46 0.312
333
ATM095 Autoimmune Disease 61 0.312
334
HYP006 Hypertensive Heart Disease 48 0.312
335
NPH010 Nephrosclerosis 50 0.312
336
ESP020 Esophageal Atresia 59 0.312
337
c LCL006 Localized Scleroderma 64 0.312
338
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.296
339
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.296
340
TND004 Tendinopathy 45 0.296
341
HYP025 Hyperphosphatemia 47 0.296
342
MSC007 Muscle Hypertrophy 64 0.296
343
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.296
344
P ALC033 Alcohol Use Disorder 67 0.296
345
P GRV001 Graves' Disease 54 0.296
346
NWB001 Newborn Respiratory Distress Syndrome 56 0.296
347
ILS001 Ileus 49 0.296
348
P OST135 Osteogenesis Imperfecta, Type I 60 0.279
349
PRX015 Paroxysmal Extreme Pain Disorder 56 0.279
350
P PLV020 Pelvic Organ Prolapse 57 0.279
352
P AST005 Asthma 75 0.279
353
c HYP595 Hypertension, Essential 84 0.279
354
ESP021 Esophageal Cancer 84 0.279
355
c ACT075 Acute Myocardial Infarction 55 0.279
356
CTN020 Cutaneous Sclerosis 16 0.279
357
THY029 Thyroid Carcinoma 55 0.279
358
P ATR011 Atrial Fibrillation 66 0.261
359
ART140 Arteries, Anomalies of 52 0.261
360
LPP008 Lipoprotein Quantitative Trait Locus 65 0.261
361
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.261
362
CMB007 Combined Immunodeficiency 56 0.261
363
P RCT021 Rectum Cancer 54 0.261
364
EXT006 Extrahepatic Cholestasis 41 0.261
365
P LTR001 Lateral Sclerosis 57 0.261
366
CL1007 Col1a1/2 Osteogenesis Imperfecta 25 0.261
367
ULC004 Ulcerative Colitis 74 0.261
368
PPT005 Peptic Ulcer Disease 58 0.261
369
P MSC003 Muscular Atrophy 52 0.261
370
P CLS054 Classic Ehlers-Danlos Syndrome 57 0.261
371
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.241
372
P SLP006 Sleep Apnea 69 0.241
373
P RHM011 Rheumatoid Arthritis 81 0.241
374
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.241
375
MCC012 Mccune-Albright Syndrome 69 0.241
376
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.241
377
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.241
378
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.241
379
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.241
380
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.241
381
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.241
382
c HMC039 Hemochromatosis, Type 1 73 0.241
383
P MYC084 Mycobacterium Tuberculosis 1 68 0.241
384
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.241
385
LPT014 Leptin Deficiency or Dysfunction 77 0.241
386
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.241
387
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.241
388
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.241
389
OBS082 Obstructive Nephropathy 41 0.241
390
P VSC007 Vascular Disease 62 0.241
391
CRB037 Cerebral Palsy 66 0.241
392
P TRN020 Turner Syndrome 67 0.241
393
LYM027 Lymphopenia 56 0.241
394
BRN002 Bronchiolitis 57 0.241
395
KHN001 Kuhnt-Junius Degeneration 48 0.241
396
QDR001 Quadriplegia 49 0.241
397
ORL004 Oral Submucous Fibrosis 56 0.241
398
END086 End Stage Renal Disease 54 0.241
399
P CRN028 Corneal Ulcer 47 0.241
400
P HMR005 Hemorrhoid 49 0.241
401
SPS057 Spasticity 43 0.241
402
c ATS007 Autism Spectrum Disorder 71 0.220
403
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.220
404
CRH005 Crohn's Colitis 53 0.220
405
UMB002 Umbilical Hernia 46 0.220
406
P ATS364 Autism 72 0.220
407
ALC007 Alcohol Dependence 65 0.220
408
c BRN108 Branchiootic Syndrome 1 63 0.220
409
P CHN012 Chondrosarcoma 56 0.220
410
WRN001 Werner Syndrome 69 0.220
411
P LNG064 Lung Cancer Susceptibility 3 69 0.220
412
P DDN001 Duodenal Ulcer 52 0.220
413
BRN012 Bronchiolitis Obliterans 56 0.220
414
CHL067 Cholecystitis 59 0.220
415
LPD008 Lipid Metabolism Disorder 61 0.220
416
FBR047 Fibromyalgia 57 0.220
417
AMN001 Amenorrhea 53 0.220
418
P ADN016 Adenocarcinoma 63 0.220
419
P PSD015 Pseudohypoparathyroidism 54 0.220
420
P MYP004 Myopathy 67 0.220
421
PLC005 Placental Insufficiency 55 0.220
422
P FNC004 Fanconi Syndrome 60 0.220
423
P HYP040 Hypospadias 51 0.220
424
TTN003 Tetanus 64 0.220
425
P RNL007 Renal Tubular Acidosis 52 0.220
426
P PLM034 Pulmonary Emphysema 58 0.220
427
P AVS003 Avascular Necrosis 41 0.220
428
P PRC019 Precocious Puberty 48 0.220
429
GLL048 Glial Tumor 51 0.220
430
CRS005 Crest Syndrome 36 0.197
431
ASP007 Aspiration Pneumonia 49 0.197
432
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 63 0.197
433
EHL052 Ehlers-Danlos Syndrome, Vascular Type 63 0.197
434
MYX004 Myxedema 43 0.197
435
c MYT020 Myotonic Dystrophy 2 57 0.197
436
HMC014 Homocysteinemia 52 0.197
437
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.197
439
IMM167 Immune Deficiency Disease 76 0.197
440
c MCL062 Mucolipidosis Ii Alpha/beta 69 0.197
441
P HYP726 Hypercalcemia, Infantile, 1 58 0.197
442
CLF027 Cleft Palate, Isolated 64 0.197
443
HRW001 Hair Whorl 35 0.197
444
PRT010 Parathyroid Carcinoma 68 0.197
445
GYR004 Gyrate Atrophy of Choroid and Retina 58 0.197
446
TRY001 Trypanosomiasis 50 0.197
447
P CRN024 Corneal Disease 43 0.197
448
P VNS003 Venous Insufficiency 54 0.197
449
P MCL001 Mucolipidosis 49 0.197
450
CHR431 Chronic Venous Insufficiency 48 0.197
451
c ACT071 Acute Kidney Failure 60 0.197
452
IDP011 Idiopathic Interstitial Pneumonia 59 0.197
453
CLC006 Calcinosis 47 0.197
454
P SPN046 Spinal Muscular Atrophy 62 0.197
455
BCT022 Bacterial Infectious Disease 55 0.197
456
P PYL005 Pyelonephritis 56 0.197
457
ART017 Aortic Disease 49 0.197
458
TRC005 Tracheal Stenosis 43 0.197
459
P ACN011 Acne 55 0.197
460
P PNM007 Pneumonia 64 0.197
461
ART074 Aortic Dissection 53 0.197
462
P BRS044 Breast Adenocarcinoma 58 0.197
463
c CHR098 Chronic Pyelonephritis 34 0.197
464
LPR001 Lepromatous Leprosy 49 0.197
465
KRT002 Keratomalacia 54 0.197
466
RHM001 Rheumatic Fever 59 0.197
467
DYS015 Dysentery 49 0.197
468
P MLN008 Melanoma 75 0.197
469
DCB001 Decubitus Ulcer 61 0.197
470
CLF001 Cleft Lip 54 0.197
471
CRV025 Cervical Incompetence 35 0.197
472
P PLY018 Polycythemia 56 0.197
473
ETN001 Eating Disorder 59 0.197
474
CRD016 Cardiac Rupture 34 0.197
475
PRQ001 Paraquat Lung 16 0.197
476
P ENC018 Encephalopathy 62 0.197
477
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.171
478
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.171
479
MCC013 Mucocutaneous Ulceration, Chronic 40 0.171
480
DFC004 Deficiency Anemia 74 0.171
481
P CRN300 Coronary Heart Disease 1 73 0.171
482
GLY010 Glycine Encephalopathy 57 0.171
483
PNG002 Pain Agnosia 51 0.171
484
P BTH005 Bethlem Myopathy 1 62 0.171
485
c EHL073 Ehlers-Danlos Syndrome, Classic Type, 1 54 0.171
486
P PRS040 Prostate Cancer 95 0.171
487
P CRC039 Coarctation of Aorta 46 0.171
488
P TMP003 Temporal Arteritis 68 0.171
489
P BLD134 Bladder Cancer 79 0.171
490
c OST126 Osteopetrosis, Autosomal Recessive 1 51 0.171
491
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.171
492
PRP027 Peripheral Vascular Disease 71 0.171
493
P CRP001 Carpal Tunnel Syndrome 65 0.171
494
c HYP248 Hyperprolinemia, Type I 43 0.171
495
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.171
496
c LKM063 Leukemia, Chronic Myeloid 70 0.171
497
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 52 0.171
498
PRS129 Prostatic Hyperplasia, Benign 48 0.171
499
P MYG005 Myoglobinuria 40 0.171
500
CHK001 Chikungunya 60 0.171
501
P FBR025 Fibrochondrogenesis 55 0.171
502
ESP002 Esophageal Varix 51 0.171
503
DPH001 Diphtheria 59 0.171
504
HPT019 Hepatic Encephalopathy 59 0.171
505
c ATM011 Autoimmune Hepatitis 62 0.171
506
P GCH001 Gaucher's Disease 69 0.171
507
P EPD016 Epidermolysis Bullosa 53 0.171
508
NNS002 Nonspecific Interstitial Pneumonia 42 0.171
509
SQM006 Squamous Cell Carcinoma 59 0.171
510
URT037 Urethral Stricture 42 0.171
511
P PLM006 Pulmonary Alveolar Proteinosis 53 0.171
512
LYM021 Lymphadenitis 55 0.171
513
MNR003 Mineral Metabolism Disease 37 0.171
514
DFF003 Diffuse Scleroderma 41 0.171
515
DFF002 Diffuse Pulmonary Fibrosis 27 0.171
516
MTR002 Mitral Valve Insufficiency 51 0.171
517
HPT014 Hepatorenal Syndrome 49 0.171
518
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.171
519
MDD018 Middle East Respiratory Syndrome 44 0.171
520
BLR001 Biliary Atresia 55 0.171
521
MYM001 Myoma 54 0.171
522
c HPT016 Hepatitis B 62 0.171
523
CNS004 Constipation 56 0.171
524
HRT012 Heart Valve Disease 53 0.171
525
PRS021 Prostatic Adenoma 43 0.171
526
PLR007 Pleural Empyema 50 0.171
527
GNG013 Gingivitis 59 0.171
528
P TRT010 Teratoma 50 0.171
529
EMB004 Embryonal Carcinoma 55 0.171
530
P HYP061 Hypertrophic Cardiomyopathy 68 0.171
531
CNN003 Conn's Syndrome 77 0.171
532
CRN017 Coronary Thrombosis 46 0.171
533
CRT017 Cartilage Disease 52 0.171
534
P NTR004 Neutropenia 62 0.171
535
P GND004 Gonadal Dysgenesis 46 0.171
536
HPT004 Hepatic Coma 43 0.171
537
P ART018 Aortic Valve Insufficiency 52 0.171
538
c INH020 Inherited Metabolic Disorder 47 0.171
539
P MST009 Mastocytosis 64 0.171
540
c JVN010 Juvenile Rheumatoid Arthritis 52 0.171
541
P VSC011 Vasculitis 61 0.171
542
P NRF002 Neurofibromatosis 60 0.171
543
HYP057 Hypervitaminosis D 37 0.171
544
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.171
545
PTT037 Pituitary Tumors 44 0.171
546
WLL004 Wallerian Degeneration 38 0.171
547
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.171
548
ORN004 Ornithinemia 13 0.171
549
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.171
550
TRM010 Traumatic Brain Injury 50 0.171
551
ARG004 Argyria 26 0.171
552
c CHR417 Chronic Graft Versus Host Disease 55 0.171
553
c ACT134 Acute Liver Failure 57 0.171
554
P SCL048 Sclerosteosis 58 0.139
555
MYL020 Myelomeningocele 51 0.139
556
P CNG539 Congenital Disorder of Glycosylation with Defective Fucosylation 1 25 0.139
557
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.139
558
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.139
559
P BRC015 Bruck Syndrome 48 0.139
560
P ALZ034 Alzheimer Disease 87 0.139
561
c ART115 Aortic Valve Disease 1 72 0.139
562
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.139
563
P CLC063 Celiac Disease 1 65 0.139
564
ESN015 Eosinophilic Fasciitis 46 0.139
565
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.139
566
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.139
567
PLY150 Polykaryocytosis Inducer 29 0.139
568
P CMR001 Camurati-Engelmann Disease 58 0.139
569
SPR004 Supravalvular Aortic Stenosis 57 0.139
570
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 0.139
571
PRP082 Porphyria, Congenital Erythropoietic 56 0.139
572
P PSD087 Pseudoxanthoma Elasticum 66 0.139
573
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.139
574
P GST053 Gastric Cancer 82 0.139
575
SPS007 Spastic Cerebral Palsy 45 0.139
576
VLV047 Volvulus of Midgut 55 0.139
577
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.139
578
ANN002 Anencephaly 57 0.139
579
LYS003 Lysinuric Protein Intolerance 57 0.139
580
c DPH024 Diaphragmatic Hernia, Congenital 63 0.139
581
CLL041 Collagenoma, Familial Cutaneous 20 0.139
582
MYL013 Myeloperoxidase Deficiency 44 0.139
583
c BRC047 Bruck Syndrome 1 32 0.139
584
c OST164 Osteoporosis, Juvenile 55 0.139
585
c BNM031 Bone Mineral Density Quantitative Trait Locus 17 15 0.139
586
c OPT053 Optic Atrophy 1 62 0.139
587
CHR003 Cherubism 57 0.139
588
c OST131 Osteopetrosis, Autosomal Dominant 2 52 0.139
589
c PNC108 Pancreatitis, Hereditary 68 0.139
590
CHD004 Chudley-Mccullough Syndrome 47 0.139
591
RFL001 Reflex Sympathetic Dystrophy 51 0.139
592
PNB004 Panbronchiolitis, Diffuse 34 0.139
593
PLL012 Pollen Allergy 44 0.139
594
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.139
595
c ACT249 Acute Asthma 40 0.139
596
P PLY041 Polymyositis 58 0.139
597
P SDR002 Siderosis 42 0.139
598
P LCT002 Lactose Intolerance 51 0.139
599
P SHR001 Short Bowel Syndrome 53 0.139
600
DNT002 Dentine Erosion 18 0.139
601
P LKM002 Leukemia 65 0.139
602
OST015 Osteochondrodysplasia 60 0.139
603
DNT012 Dental Caries 53 0.139
604
THR004 Thrombocytosis 52 0.139
605
HYP068 Hyperostosis 47 0.139
606
PRP030 Purpura 54 0.139
607
GLB002 Glioblastoma 67 0.139
608
SKN005 Skin Atrophy 41 0.139
609
IRR003 Irritant Dermatitis 47 0.139
610
BRD003 Bird Fancier's Lung 33 0.139
611
P BNC003 Bone Cancer 58 0.139
612
HYP014 Hyperuricemia 51 0.139
613
P DRR001 Diarrhea 55 0.139
614
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.139
615
SYS004 Systemic Mastocytosis 62 0.139
616
P HRM001 Hermansky-Pudlak Syndrome 65 0.139
617
THR012 Thoracic Cancer 44 0.139
618
URN010 Urinary Tract Obstruction 55 0.139
619
HYP063 Hypersplenism 51 0.139
620
P PLY011 Polycystic Ovary Syndrome 57 0.139
621
c ATM022 Autoimmune Myocarditis 35 0.139
622
BRD005 Borderline Leprosy 28 0.139
623
CHN011 Chondromalacia 38 0.139
624
CRC021 Carcinosarcoma 62 0.139
625
ORC001 Orchitis 43 0.139
626
ANV001 Anovulation 46 0.139
627
P CHR012 Chronic Granulomatous Disease 69 0.139
628
TRT001 Teratocarcinoma 41 0.139
629
P DNT011 Dentinogenesis Imperfecta 51 0.139
630
HYP043 Hyperandrogenism 47 0.139
631
GST033 Gestational Diabetes 60 0.139
632
GLC003 Glucose Intolerance 53 0.139
633
MCR013 Microphthalmia 59 0.139
634
END028 Endemic Goiter 36 0.139
635
END062 Endometrial Hyperplasia 47 0.139
636
OLG003 Oligohydramnios 50 0.139
637
FRM003 Farmer's Lung 41 0.139
638
ALG001 Algoneurodystrophy 37 0.139
639
ACT040 Acute Poststreptococcal Glomerulonephritis 35 0.139
640
AZS001 Azoospermia 45 0.139
641
NNT010 Nontoxic Goiter 32 0.139
642
NDL007 Nodular Goiter 48 0.139
643
CRN027 Corneal Neovascularization 47 0.139
644
P END046 Endometritis 46 0.139
645
CRB004 Cerebral Artery Occlusion 45 0.139
646
DVR002 Diverticulitis 46 0.139
647
GSG001 Gas Gangrene 52 0.139
648
MCR004 Macroglobulinemia 48 0.139
649
BNT001 Banti's Syndrome 21 0.139
650
PRP007 Priapism 46 0.139
651
FSC004 Fasciitis 49 0.139
652
PPT002 Peptic Ulcer Perforation 34 0.139
653
P NRB001 Neuroblastoma 66 0.139
654
ULC005 Ulcer of Lower Limbs 37 0.139
655
GLM045 Glioma 62 0.139
656
NRF007 Neurofibroma 63 0.139
657
MSL001 Measles 61 0.139
658
GST039 Gastroduodenitis 37 0.139
659
P VND001 Vein Disease 42 0.139
660
PRS037 Periostitis 40 0.139
661
P DST107 Distal Renal Tubular Acidosis 48 0.139
662
GRN017 Granulocytopenia 42 0.139
663
c JVN025 Juvenile Primary Osteoporosis 21 0.139
664
c CNT075 Central Precocious Puberty 53 0.139
665
P HRP006 Herpes Simplex 65 0.139
666
EXP004 Exophthalmos 50 0.139
667
DST006 Diastolic Heart Failure 45 0.139
668
ANX004 Anoxia 40 0.139
669
HYP056 Hypoglycemia 65 0.139
670
FKB002 Fkbp14 Kyphoscoliotic Ehlers-Danlos Syndrome 8 0.139
671
HYP706 Hypermobile Ehlers-Danlos Syndrome 54 0.139
672
P CNG048 Congenital Hepatic Fibrosis 36 0.139
673
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.139
674
BRN071 Brain Injury 50 0.139
675
c RNG015 Ring Chromosome 2 22 0.139
676
DYS073 Dysphagia 53 0.139
677
P HYP265 Hypotonia 42 0.139
678
PRM329 Premature Aging 36 0.139
679
ORG002 Organic Acidemia 43 0.099
680
ACT119 Acute Promyelocytic Leukemia 62 0.099
681
SXL003 Sexual Disorder 49 0.099
682
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.099
684
HYP540 Hypertension, Diastolic 38 0.099
685
ASC010 Ascaris Lumbricoides Infection 49 0.099
686
P LYM118 Lymphoma 66 0.099
687
P GLL020 Gallbladder Disease 57 0.099
688
PRT119 Protrusio Acetabuli 33 0.099
689
ACH004 Achondroplasia 65 0.099
690
c WLM013 Wilms Tumor 1 65 0.099
691
CHR072 Chordoma 56 0.099
692
EHL061 Ehlers-Danlos Syndrome, Cardiac Valvular Type 46 0.099
693
c EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 51 0.099
694
EHL079 Ehlers-Danlos Syndrome, Dermatosparaxis Type 52 0.099
695
DWN001 Down Syndrome 70 0.099
696
c PSD104 Pseudohypoparathyroidism, Type Ii 31 0.099
697
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.099
698
CHD001 Chediak-Higashi Syndrome 66 0.099
699
c NRF024 Neurofibromatosis, Type I 76 0.099
700
OTT002 Otitis Media 70 0.099
701
c PGT007 Paget Disease of Bone 3 39 0.099
702
P HYP534 Hypomagnesemia 3, Renal 46 0.099
703
MYS016 Myosclerosis, Autosomal Recessive 32 0.099
704
P ALK019 Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 1 17 0.099
705
HND015 Hand Skill, Relative 29 0.099
706
HRN026 Hernia, Hiatus 46 0.099
707
CRD132 Cardiac Conduction Defect 59 0.099
708
HYP784 Hypogonadism, Male 43 0.099
709
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.099
710
DGR001 Digeorge Syndrome 62 0.099
711
P GLC113 Galactosemia I 65 0.099
712
c STC015 Stickler Syndrome, Type I 50 0.099
713
GST092 Gastroesophageal Reflux 59 0.099
714
BSL036 Basal Cell Nevus Syndrome 73 0.099
715
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.099
716
P BRS047 Breast Cancer 97 0.099
717
P CLR023 Colorectal Cancer 100 0.099
718
P MLT020 Multiple Sclerosis 79 0.099
719
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.099
720
c HYP272 Hypercholesterolemia, Familial, 3 46 0.099
721
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.099
722
c PGT009 Paget Disease of Bone 2, Early-Onset 34 0.099
723
BSM002 Bosma Arhinia Microphthalmia Syndrome 44 0.099
724
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.099
725
SRC015 Sarcosinemia 38 0.099
726
P NSP012 Nasopharyngeal Carcinoma 60 0.099
727
RST023 Resting Heart Rate, Variation in 40 0.099
728
ANX010 Anxiety 70 0.099
729
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.099
730
c JVN061 Juvenile Arthritis 56 0.099
731
c CNG006 Congenital Hypothyroidism 63 0.099
732
c OST133 Osteogenesis Imperfecta, Type Xi 38 0.099
733
CHP002 Chops Syndrome 47 0.099
734
c MYP117 Myopia 25, Autosomal Dominant 19 0.099
735
P CMB108 Combined Osteogenesis Imperfecta and Ehlers-Danlos Syndrome 1 20 0.099
736
CYN002 Cyanosis, Transient Neonatal 43 0.099
737
c HRM009 Hermansky-Pudlak Syndrome 6 46 0.099
738
HYP114 Hypertensive Nephropathy 35 0.099
739
P EXN002 Exanthem 58 0.099
741
c PNC106 Pancreatic Agenesis 1 51 0.099
742
PLY001 Polycythemia Vera 69 0.099
743
ACR008 Acrocallosal Syndrome 69 0.099
744
P UTR058 Uterine Anomalies 47 0.099
745
c CRP023 Carpenter Syndrome 1 59 0.099
746
ACR034 Acrogeria, Gottron Type 27 0.099
747
KLD003 Keloid Formation 34 0.099
748
KRT019 Keratitis, Hereditary 66 0.099
749
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.099
750
KPS004 Kaposi Sarcoma 76 0.099
751
P HYP058 Hypervitaminosis a 47 0.099
752
HYP596 Hypophosphatasia, Childhood 47 0.099
753
HRT031 Hartnup Disorder 51 0.099
754
CHY002 Chylomicron Retention Disease 64 0.099
755
P LKM062 Leukemia, Acute Lymphoblastic 69 0.099
756
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.099
757
CHR222 Chromosome 1p36 Deletion Syndrome 48 0.099
758
c ART101 Aortic Valve Disease 2 65 0.099
759
c HRM017 Hermansky-Pudlak Syndrome 2 55 0.099
760
LPT006 Leptin Receptor Deficiency 50 0.099
761
c PCH010 Pachyonychia Congenita 3 43 0.099
762
c PRX054 Peroxisome Biogenesis Disorder 12a 33 0.099
763
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.099
764
RBF001 Riboflavin Deficiency 49 0.099
765
c OST128 Osteogenesis Imperfecta, Type Xii 36 0.099
766
BRK010 Burkitt Lymphoma 65 0.099
767
P LKM071 Leukemia, Chronic Lymphocytic 74 0.099
768
P OCL013 Oculodentodigital Dysplasia 66 0.099
769
P PRK057 Parkinson Disease, Late-Onset 79 0.099
770
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.099
771
c HYP243 Hyperparathyroidism 1 48 0.099
772
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.099
773
HYP748 Hypertelorism 46 0.099
774
THY069 Thyroid Hormone Resistance, Selective Pituitary 36 0.099
775
CHL131 Chlorpropamide-Alcohol Flushing 21 0.099
776
ELS002 Elastosis Perforans Serpiginosa 33 0.099
777
P HYP733 Hypercalciuria, Absorptive, 2 45 0.099
778
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.099
779
c OST121 Osteogenesis Imperfecta, Type Iv 48 0.099
780
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 46 0.099
781
c OST122 Osteogenesis Imperfecta, Type Iii 57 0.099
782
DMN042 Diaminopentanuria 14 0.099
783
LKN005 Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema 20 0.099
784
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.099
785
ORT008 Orotic Aciduria 56 0.099
786
c DMN005 Diamond-Blackfan Anemia 2 28 0.099
787
BRL010 Buruli Ulcer 45 0.099
788
ADN027 Adenomyosis 59 0.099
789
FRY006 Fryns Microphthalmia Syndrome 52 0.099
790
P MLT008 Multinodular Goiter 41 0.099
791
c SVR003 Severe Congenital Neutropenia 59 0.099
792
P FTL001 Fetal Alcohol Syndrome 55 0.099
793
CHR005 Chorioamnionitis 50 0.099
794
BNR001 Bone Remodeling Disease 29 0.099
795
FBR010 Fibrogenesis Imperfecta Ossium 25 0.099
796
P ACH011 Achondrogenesis 53 0.099
797
c HRD202 Hereditary Lymphedema I 54 0.099
798
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.099
799
P CLC057 Cole-Carpenter Syndrome 41 0.099
800
PRM237 Primary Hypomagnesemia 44 0.099
801
P SNS001 Sensorineural Hearing Loss 60 0.099
802
PRP074 Peripheral Resistance to Thyroid Hormones 10 0.099
803
THR024 Thrombosis 56 0.099
804
ORN001 Ornithosis 39 0.099
805
P PRK039 Parkinsonism 55 0.099
806
DSS009 Disseminated Intravascular Coagulation 56 0.099
807
VTM033 Vitamin K Deficiency Bleeding 49 0.099
808
PRP080 Peripheral Artery Disease 54 0.099
809
ANT017 Anthracosilicosis 24 0.099
810
CLN003 Clonorchiasis 42 0.099
811
PST028 Post-Traumatic Stress Disorder 58 0.099
812
CLN015 Colon Adenocarcinoma 64 0.099
813
BLR008 Bilirubin Metabolic Disorder 57 0.099
814
P GLY013 Glycogen Storage Disease 59 0.099
815
P MYT023 Myotonia Congenita 55 0.099
816
P BNG095 Benign Giant Cell Tumor 43 0.099
817
NRM004 Neuroma 49 0.099
818
CPL001 Capillariasis 26 0.099
819
GNT001 Giant Cell Reparative Granuloma 40 0.099
820
c MLG084 Malignant Fibrous Histiocytoma 62 0.099
821
KRT009 Keratosis 52 0.099
822
BRN014 Bronchopneumonia 52 0.099
823
RHM028 Rheumatic Heart Disease 55 0.099
824
CNS002 Constrictive Pericarditis 39 0.099
825
P ECL001 Eclampsia 52 0.099
826
P BLD062 Bile Duct Cancer 69 0.099
827
IMM001 Immune-Complex Glomerulonephritis 36 0.099
828
MST004 Mast Cell Neoplasm 41 0.099
829
INT002 Intermittent Claudication 61 0.099
830
VLK001 Volkmann Contracture 23 0.099
831
SCL002 Scleredema Adultorum 45 0.099
832
P CTS001 Cutis Laxa 64 0.099
833
TRC026 Tracheal Disease 43 0.099
834
INF013 Inferior Myocardial Infarction 33 0.099
835
P INT068 Intestinal Disease 53 0.099
836
PTT009 Pituitary Gland Disease 52 0.099
837
LPT001 Leptospirosis 65 0.099
838
P MTR014 Motor Neuron Disease 65 0.099
839
RYS001 Reye Syndrome 49 0.099
840
LYM017 Lyme Disease 63 0.099
841
P EPL164 Epilepsy 70 0.099
842
STR008 Strongyloidiasis 52 0.099
843
HMP005 Hemiplegia 53 0.099
844
SPS004 Spastic Quadriplegia 39 0.099
845
c FML021 Familial Hypercholesterolemia 71 0.099
846
SKN006 Skin Sarcoidosis 42 0.099
847
PNC034 Pancreas Disease 49 0.099
848
DRM006 Dermatitis 61 0.099
849
RTR001 Retrograde Amnesia 41 0.099
850
P HYP077 Hypertrichosis 48 0.099
851
SPN035 Spindle Cell Sarcoma 51 0.099
852
ANT010 Anterior Compartment Syndrome 21 0.099
853
ASC001 Ascaridiasis 36 0.099
854
GLS001 Gliosarcoma 63 0.099
855
GRN007 Granuloma Annulare 43 0.099
856
P JNC001 Junctional Epidermolysis Bullosa 54 0.099
857
P SKN015 Skin Carcinoma 71 0.099
858
EXT007 Extracutaneous Mastocytoma 38 0.099
859
GLC008 Glucose Metabolism Disease 40 0.099
860
CRN030 Coronary Stenosis 50 0.099
861
RDC002 Radiculopathy 51 0.099
862
DGN002 Degenerative Myopia 31 0.099
863
CLB002 Clubfoot 50 0.099
864
AMN003 Amnestic Disorder 53 0.099
865
MST005 Mastitis 52 0.099
866
GRD001 Giardiasis 46 0.099
867
P HYD006 Hydrocephalus 62 0.099
868
PLM011 Plummer's Disease 34 0.099
869
ANC001 Ancylostomiasis 39 0.099
871
BNS007 Bone Sarcoma 50 0.099
872
CMM005 Common Cold 55 0.099
873
P MCR010 Microcephaly 59 0.099
874
NRG002 Neurogenic Bladder 54 0.099
875
LWC001 Low Compliance Bladder 44 0.099
876
P THR014 Thrombocytopenia 66 0.099
877
HST011 Histoplasmosis 54 0.099
878
IRT001 Iritis 45 0.099
879
OBS004 Obstructive Hydrocephalus 44 0.099
880
BCT004 Bacteriuria 48 0.099
881
P HYP035 Hypophosphatasia 61 0.099
882
P PRM018 Primary Hypertrophic Osteoarthropathy 56 0.099
883
TRC012 Trichuriasis 44 0.099
884
ALC010 Alcoholic Cardiomyopathy 42 0.099
885
P DMN002 Dementia 65 0.099
886
HYD002 Hydronephrosis 58 0.099
887
SRC014 Sarcoma 64 0.099
888
PRT037 Pertussis 49 0.099
889
CYS005 Cysticercosis 60 0.099
890
CHL004 Cholelithiasis 48 0.099
891
P DRM010 Dermatomyositis 61 0.099
892
VRC001 Varicocele 48 0.099
893
SCB001 Scabies 49 0.099
894
SCR011 Scrapie 39 0.099
895
P HML002 Hemolytic Anemia 62 0.099
896
MXD005 Mixed Connective Tissue Disease 57 0.099
897
CHR074 Choriocarcinoma 46 0.099
898
P LCT001 Lactic Acidosis 50 0.099
899
PLG002 Plague 58 0.099
900
CRB031 Cerebral Arterial Disease 35 0.099
901
P ESN008 Eosinophilic Pneumonia 50 0.099
902
CRB039 Cerebrovascular Disease 65 0.099
903
SPN027 Spinal Stenosis 58 0.099
904
P MYL006 Myeloid Leukemia 60 0.099
905
FML031 Female Stress Incontinence 39 0.099
906
P FBR003 Fibrous Histiocytoma 43 0.099
907
P CMP008 Compartment Syndrome 49 0.099
908
P OVR046 Ovarian Cyst 43 0.099
909
HYP141 Hyperphenylalaninemia 42 0.099
910
PLM035 Pulmonary Eosinophilia 49 0.099
911
P BRN022 Bronchiectasis 59 0.099
912
YLL002 Yellow Fever 61 0.099
913
TXC010 Toxic Myocarditis 23 0.099
914
P ZLL001 Zellweger Syndrome 65 0.099
915
TRC020 Tracheitis 43 0.099
916
CRP002 Croup 42 0.099
917
CHR066 Chronic Fatigue Syndrome 59 0.099
918
CNG065 Congenital Contractures 27 0.099
919
LYM019 Lymphosarcoma 46 0.099
920
SYS003 Systolic Heart Failure 49 0.099
921
DBT010 Diabetic Neuropathy 54 0.099
922
P LPS004 Lupus Erythematosus 61 0.099
923
VSC002 Vascular Dementia 59 0.099
924
FBR083 Fibrous Dysplasia/mccune-Albright Syndrome 27 0.099
925
BNM005 Bone Marrow Necrosis 25 0.099
926
CHF001 Chief Cell Adenoma 22 0.099
927
GST050 Gastrointestinal System Disease 55 0.099
928
HML018 Homologous Wasting Disease 21 0.099
929
P KYP005 Kyphoscoliotic Ehlers-Danlos Syndrome 40 0.099
930
P SZR006 Seizure Disorder 69 0.099
931
P DBT005 Diabetes Insipidus 54 0.099
932
c BCT007 Bacterial Meningitis 55 0.099
933
P MNN013 Meningitis 65 0.099
934
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.099
935
c ATS282 Autosomal Recessive Malignant Osteopetrosis 45 0.099
936
CRC006 Carcinoid Syndrome 55 0.099
937
OVR094 Ovarian Epithelial Cancer 39 0.099
938
IRR002 Irritable Bowel Syndrome 64 0.099
939
PNS013 Panostotic Fibrous Dysplasia 8 0.099
940
CHR178 Chromosomal Triplication 33 0.099
941
P FML187 Familial Hypertension 34 0.099
942
P GNR008 Generalized Resistance to Thyroid Hormone 23 0.099
943
HVY002 Heavy Metal Poisoning 22 0.099
944
LYM035 Lymphangiectasis 30 0.099
945
P MRC003 Mercury Poisoning 48 0.099
946
c HRD219 Hereditary Distal Renal Tubular Acidosis 26 0.099
947
P ACT105 Acute Mountain Sickness 52 0.099
948
PNM013 Pneumococcal Meningitis 43 0.099
949
P SKL032 Skeletal Muscle Disease