Search results for Triglycerides Group A

1455 hits were found for Triglycerides Group A

# Family MCID Name MIFTS Score
1
c FNC027 Fanconi Anemia, Complementation Group a 80 41.556
2
c BLD140 Blood Group, I System 47 38.256
3
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 36.537
4
CHN055 Chanarin-Dorfman Syndrome 61 32.317
5
c TYP009 Type 2 Diabetes Mellitus 91 32.029
6
P HYP750 Hypertriglyceridemia, Familial 61 31.673
7
P DBT009 Diabetes Mellitus 67 30.826
8
ABT001 Abetalipoproteinemia 68 28.562
9
LPD008 Lipid Metabolism Disorder 61 28.473
10
c HYP836 Hypercholesterolemia, Familial, 1 73 27.846
11
NNL005 Non-Alcoholic Fatty Liver Disease 63 25.553
12
FTT001 Fatty Liver Disease 61 25.419
13
P CRN300 Coronary Heart Disease 1 73 24.769
14
P BRS047 Breast Cancer 97 23.856
15
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 23.823
16
LPP008 Lipoprotein Quantitative Trait Locus 65 23.728
17
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 23.658
18
RPD005 Rapidly Involuting Congenital Hemangioma 48 23.392
19
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 23.285
20
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 22.631
21
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 22.631
22
48X005 48,xyyy 39 22.605
23
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 22.581
24
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 22.581
25
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 22.461
26
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 22.461
27
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 22.461
28
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 22.461
29
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 22.460
30
ART140 Arteries, Anomalies of 52 21.949
31
P HRT032 Heart Disease 84 21.314
32
c HYP595 Hypertension, Essential 84 20.507
33
ATH013 Atherosclerosis Susceptibility 63 20.309
34
P LVR013 Liver Disease 68 20.269
35
ISC004 Ischemia 61 18.962
36
HPT025 Hepatic Lipase Deficiency 47 18.939
37
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 18.798
38
PLM129 Pulmonary Disease, Chronic Obstructive 74 17.945
39
AGN016 Aging 53 17.896
40
P SCH015 Schizophrenia 74 17.884
41
P HPT021 Hepatitis 68 17.841
42
P TMR010 Tumor Predisposition Syndrome 69 17.824
43
INH023 Inherited Cancer-Predisposing Syndrome 53 17.766
44
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 17.765
45
P KDN018 Kidney Disease 71 17.719
46
P LNG032 Lung Cancer 98 17.582
47
STR067 Stroke, Ischemic 79 17.581
48
P PNC044 Pancreatitis 61 17.429
49
P LKM002 Leukemia 65 17.398
50
DPR016 Depression 64 17.393
51
c ATR087 Atrial Standstill 1 74 17.306
52
c CHR684 Chronic Kidney Disease 73 17.268
53
P MYC007 Myocardial Infarction 69 17.018
54
P ART022 Arthritis 70 16.970
55
P ALZ034 Alzheimer Disease 87 16.922
56
MNT002 Mental Depression 56 16.794
57
P PRS040 Prostate Cancer 95 16.718
58
c TYP008 Type 1 Diabetes Mellitus 77 16.535
59
c ACT027 Acute Pancreatitis 60 16.486
60
P SZR006 Seizure Disorder 69 16.375
61
P CLR023 Colorectal Cancer 100 16.202
62
NTR007 Neutral Lipid Storage Disease with Myopathy 42 16.193
63
P NTR004 Neutropenia 62 15.955
64
P AST005 Asthma 75 15.925
65
HMN044 Human Immunodeficiency Virus Type 1 76 15.787
66
OST012 Osteoarthritis 77 15.676
67
CRH001 Crohn's Disease 80 15.671
68
DFC004 Deficiency Anemia 74 15.633
69
P EPL164 Epilepsy 70 15.619
70
P RHM011 Rheumatoid Arthritis 81 15.559
71
P VSC007 Vascular Disease 62 15.421
72
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 15.306
73
c LKM061 Leukemia, Acute Myeloid 83 15.272
74
SPT005 Spotted Fever 49 15.116
75
c ACT075 Acute Myocardial Infarction 55 15.111
76
CRB039 Cerebrovascular Disease 65 15.101
77
P LKM062 Leukemia, Acute Lymphoblastic 69 14.939
78
HYP066 Hyperglycemia 60 14.791
79
c SML038 Small Cell Cancer of the Lung 68 14.771
80
ANX010 Anxiety 70 14.643
81
P LYM118 Lymphoma 66 14.579
82
c FML021 Familial Hypercholesterolemia 71 14.553
83
P NRP001 Neuropathy 59 14.425
84
CYS001 Cystic Fibrosis 77 14.418
85
CNG034 Congestive Heart Failure 69 14.385
86
PNG002 Pain Agnosia 51 14.293
87
LNG099 Lung Disease 62 14.190
88
P MLT020 Multiple Sclerosis 79 14.147
89
P MYL006 Myeloid Leukemia 60 14.124
90
P DRR001 Diarrhea 55 14.121
91
END086 End Stage Renal Disease 54 14.119
92
P ANR048 Aniridia 1 66 14.105
93
NNL006 Non-Alcoholic Steatohepatitis 54 14.064
94
P PRD008 Periodontitis 63 14.040
95
47X002 47,xyy 47 13.964
96
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 13.951
97
TXC005 Toxic Shock Syndrome 61 13.888
98
ALC007 Alcohol Dependence 65 13.884
99
P RHN004 Rhinitis 56 13.753
100
P MJR001 Major Depressive Disorder 68 13.726
101
DWN001 Down Syndrome 70 13.666
102
c MCR115 Microvascular Complications of Diabetes 5 65 13.620
103
DSS008 Disease of Mental Health 74 13.586
104
P GST053 Gastric Cancer 82 13.404
105
DRM006 Dermatitis 61 13.348
106
P PSR002 Psoriasis 63 13.281
107
P OVR042 Ovarian Cancer 88 13.203
108
IMM167 Immune Deficiency Disease 76 13.197
109
ANG054 Angina Pectoris 65 13.170
110
PRT251 Proteinuria, Chronic Benign 58 13.132
111
P PRS038 Personality Disorder 65 13.127
112
PST011 Pustulosis of Palm and Sole 52 13.115
113
P TRN020 Turner Syndrome 67 13.101
114
PHR003 Pharyngitis 57 13.062
115
P ALC033 Alcohol Use Disorder 67 13.000
116
c HPT001 Hepatitis C 61 12.846
117
RNL114 Renal Cell Carcinoma, Nonpapillary 79 12.839
118
P DMN002 Dementia 65 12.832
119
P HPT023 Hepatocellular Carcinoma 95 12.827
120
c PRC016 Pre-Eclampsia 64 12.820
121
c HPT003 Hepatitis a 63 12.818
122
RHB024 Rhabdomyosarcoma 2 65 12.797
123
GLC003 Glucose Intolerance 53 12.783
124
c MCR120 Microvascular Complications of Diabetes 7 47 12.778
125
P OST002 Osteoporosis 76 12.776
126
LYS012 Lysosomal Acid Lipase Deficiency 64 12.721
127
P CTR002 Cataract 59 12.692
128
BCK006 Back Pain 43 12.678
129
INT323 Intraocular Pressure Quantitative Trait Locus 63 12.640
130
P INF032 Infertility 60 12.616
131
HYP056 Hypoglycemia 65 12.585
132
P HYP086 Hypothyroidism 68 12.529
133
c MCR113 Microvascular Complications of Diabetes 3 52 12.436
134
ACQ007 Acquired Immunodeficiency Syndrome 58 12.360
135
MYL069 Myeloma, Multiple 76 12.331
136
P NRB001 Neuroblastoma 66 12.303
137
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 12.297
138
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 12.297
139
c MCR133 Microvascular Complications of Diabetes 4 41 12.258
140
c MCR130 Microvascular Complications of Diabetes 6 41 12.258
141
ADL002 Adult Syndrome 69 12.228
142
PRP027 Peripheral Vascular Disease 71 12.185
143
PRT036 Peritonitis 65 12.138
144
EPD015 Epidemic Typhus 44 12.113
145
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 12.073
146
P PNM007 Pneumonia 64 12.073
147
SRC014 Sarcoma 64 12.035
148
P PLY011 Polycystic Ovary Syndrome 57 11.988
149
CLT003 Colitis 63 11.954
150
GST033 Gestational Diabetes 60 11.928
151
ALL003 Allergic Rhinitis 66 11.919
152
BRN071 Brain Injury 50 11.846
153
c SYS001 Systemic Lupus Erythematosus 85 11.836
154
c MGR028 Migraine with or Without Aura 1 63 11.829
155
P ATR011 Atrial Fibrillation 66 11.737
156
P BPL003 Bipolar Disorder 56 11.700
157
P THR014 Thrombocytopenia 66 11.668
158
P LPS004 Lupus Erythematosus 61 11.639
159
CRV035 Cervical Cancer 72 11.579
160
CNS004 Constipation 56 11.576
161
PST028 Post-Traumatic Stress Disorder 58 11.546
162
LVR012 Liver Cirrhosis 62 11.536
163
P INF037 Inflammatory Bowel Disease 53 11.524
164
SPN035 Spindle Cell Sarcoma 51 11.510
165
ALL029 Allergic Disease 61 11.464
166
MYL009 Myelodysplastic Syndrome 67 11.448
168
c HPT016 Hepatitis B 62 11.423
169
END057 Endometrial Cancer 76 11.422
170
P MYP004 Myopathy 67 11.381
171
SPN186 Spinal Cord Injury 60 11.375
172
P SLP006 Sleep Apnea 69 11.332
173
P PNC035 Pancreatic Cancer 87 11.320
174
P PLM037 Pulmonary Hypertension 69 11.305
175
CVD001 Covid-19 59 11.250
176
P PRK057 Parkinson Disease, Late-Onset 79 11.232
177
P ACN011 Acne 55 11.221
178
P RTN008 Retinitis Pigmentosa 79 11.209
179
P DRM053 Dermatitis, Atopic 65 11.173
180
c MJR022 Major Affective Disorder 8 37 11.161
181
c MJR024 Major Affective Disorder 9 40 11.161
182
CYT002 Cytokine Deficiency 43 11.132
183
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 11.107
184
ULC004 Ulcerative Colitis 74 11.106
185
ESP021 Esophageal Cancer 84 11.103
186
P PRP019 Peripheral Nervous System Disease 57 11.102
187
P ATS364 Autism 72 11.092
188
P CHR345 Chronic Pain 50 11.034
189
P ATT013 Attention Deficit-Hyperactivity Disorder 65 11.020
190
CRB037 Cerebral Palsy 66 10.988
191
P GRF003 Graft-Versus-Host Disease 71 10.887
192
ETN001 Eating Disorder 59 10.874
193
c AMY091 Amyotrophic Lateral Sclerosis 1 87 10.837
194
XRD010 Xeroderma Pigmentosum, Variant Type 72 10.836
195
c THR092 Thrombophilia Due to Thrombin Defect 74 10.818
196
P RCT021 Rectum Cancer 54 10.818
197
c ATS007 Autism Spectrum Disorder 71 10.795
198
LYM133 Lymphoma, Hodgkin, Classic 69 10.763
199
P URN019 Urinary Tract Infection 48 10.754
200
P RSP003 Respiratory Failure 73 10.740
201
P HDC001 Headache 56 10.719
202
P PRK039 Parkinsonism 55 10.703
203
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 10.679
204
P MLN008 Melanoma 75 10.561
205
c PNS012 Paine Syndrome 60 10.559
206
P HYP061 Hypertrophic Cardiomyopathy 68 10.553
207
P ADL010 Adult Respiratory Distress Syndrome 70 10.507
208
c HPT073 Hepatitis C Virus 70 10.484
209
THR024 Thrombosis 56 10.472
210
P CNR004 Cone-Rod Dystrophy 2 74 10.467
211
P ESP024 Esophagitis 60 10.463
212
P BCL017 B-Cell Lymphoma 57 10.453
213
P OPN001 Open-Angle Glaucoma 55 10.447
214
HMN014 Human Immunodeficiency Virus Infectious Disease 54 10.429
215
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 10.391
216
c DLT002 Dilated Cardiomyopathy 79 10.364
217
TRM010 Traumatic Brain Injury 50 10.357
218
IMP005 Impotence 52 10.345
219
GST092 Gastroesophageal Reflux 59 10.290
220
P CRD119 Cardiac Arrest 68 10.264
221
MLD018 Mild Cognitive Impairment 48 10.231
222
RCK004 Rickets 64 10.207
223
SQM006 Squamous Cell Carcinoma 59 10.202
224
P ADN016 Adenocarcinoma 63 10.171
225
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 10.140
226
P EXN002 Exanthem 58 10.117
227
P BLD134 Bladder Cancer 79 10.110
228
P CRD246 Cardiovascular System Disease 55 10.101
229
P HYP838 Hyperlipidemia, Familial Combined, 3 61 10.069
230
IRN002 Iron Metabolism Disease 56 10.037
231
P MNN013 Meningitis 65 10.032
232
HYP266 Hypoxia 56 10.023
233
P ALP008 Alopecia 53 9.948
234
c PLM164 Pulmonary Hypertension, Primary, 1 75 9.916
235
SVR001 Severe Acute Respiratory Syndrome 68 9.904
236
BCT022 Bacterial Infectious Disease 55 9.894
237
MCS002 Mucositis 55 9.894
238
P NPH012 Nephrotic Syndrome 61 9.879
239
SFT003 Soft Tissue Sarcoma 43 9.861
240
P GLM007 Glomerulonephritis 59 9.845
241
FML035 Familial Hyperlipidemia 54 9.697
242
END040 Endogenous Depression 54 9.686
243
LPT014 Leptin Deficiency or Dysfunction 77 9.660
244
P LYN001 Lynch Syndrome 76 9.630
245
c ACT071 Acute Kidney Failure 60 9.580
246
MCL009 Mcleod Syndrome 45 9.573
247
c SPN225 Spondyloarthropathy 1 70 9.538
248
HLC007 Helicobacter Pylori Infection 67 9.501
249
PRS045 Prostatic Hypertrophy 53 9.467
250
ANT039 Antisynthetase Syndrome 55 9.433
251
P PLM036 Pulmonary Fibrosis 65 9.401
252
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 9.325
253
P SBS003 Substance Abuse 54 9.294
254
GLB002 Glioblastoma 67 9.273
255
PLM134 Pulmonary Fibrosis, Idiopathic 76 9.271
256
P ART021 Arteriosclerosis 53 9.270
257
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 9.242
258
PRS021 Prostatic Adenoma 43 9.228
259
P SCK005 Sickle Cell Disease 56 9.214
260
HRW001 Hair Whorl 35 9.175
261
PRS129 Prostatic Hyperplasia, Benign 48 9.135
262
MLR004 Malaria 77 9.134
263
THY029 Thyroid Carcinoma 55 9.073
264
P INF038 Influenza 68 9.051
265
c HYP724 Hyperlipoproteinemia, Type Iii 66 9.042
266
c ACT068 Acute Cystitis 60 9.037
267
KRT002 Keratomalacia 54 8.937
268
P MDL005 Medulloblastoma 75 8.904
269
P MYC084 Mycobacterium Tuberculosis 1 68 8.886
270
c ACT073 Acute Leukemia 59 8.875
271
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 8.834
272
ADN018 Adenoma 58 8.827
273
P MCR129 Microvascular Complications of Diabetes 1 67 8.827
274
c EPS039 Episodic Pain Syndrome, Familial, 1 42 8.826
275
PLM033 Pulmonary Embolism 58 8.806
276
INS024 Insulin-Like Growth Factor I 77 8.801
277
P LTR001 Lateral Sclerosis 57 8.794
278
FBR047 Fibromyalgia 57 8.780
279
P END044 Endometriosis 62 8.775
280
P NSP012 Nasopharyngeal Carcinoma 60 8.745
281
GST045 Gastroenteritis 58 8.727
282
P ENC018 Encephalopathy 62 8.723
283
P CNJ013 Conjunctivitis 66 8.705
284
NTR005 Nutritional Deficiency Disease 60 8.660
285
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 8.624
286
DNT012 Dental Caries 53 8.562
287
LYM143 Lymphoma, Non-Hodgkin, Familial 74 8.561
288
DSS032 Disease by Infectious Agent 55 8.533
289
P ECL001 Eclampsia 52 8.520
290
DYS073 Dysphagia 53 8.500
291
NRT001 Neurotic Disorder 56 8.487
292
PRP030 Purpura 54 8.482
293
BRN024 Bronchitis 67 8.454
294
OST159 Osteogenic Sarcoma 66 8.448
295
SPS057 Spasticity 43 8.445
296
SKN016 Skin Disease 63 8.441
297
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 8.441
298
P EYD002 Eye Disease 57 8.424
299
PSY004 Psychotic Disorder 66 8.421
300
P LKM071 Leukemia, Chronic Lymphocytic 74 8.406
301
HMZ003 Homozygous Familial Hypercholesterolemia 60 8.377
302
PPT005 Peptic Ulcer Disease 58 8.375
303
PRS047 Prostatitis 57 8.337
304
OCL069 Ocular Motor Apraxia 57 8.314
305
RLP002 Relapsing-Remitting Multiple Sclerosis 56 8.289
306
GLL048 Glial Tumor 51 8.283
307
ANR040 Aneurysm 60 8.260
308
FSC004 Fasciitis 49 8.241
309
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 8.210
310
PSR001 Psoriatic Arthritis 61 8.209
311
P MSC005 Muscular Dystrophy 66 8.163
312
P VSC011 Vasculitis 61 8.152
313
c GLL024 Gallbladder Disease 1 53 8.145
314
P ATX030 Ataxia-Telangiectasia 80 8.119
315
c TBR025 Tuberous Sclerosis 1 84 8.115
316
SKN019 Skin Melanoma 70 8.103
317
GNG013 Gingivitis 59 8.091
318
c BRN108 Branchiootic Syndrome 1 63 8.088
319
IRR002 Irritable Bowel Syndrome 64 8.043
320
ART016 Aortic Aneurysm 68 8.039
321
c PRD040 Periodontitis, Chronic 52 8.001
322
ENT011 Enterocolitis 55 7.968
323
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 7.964
324
HMP009 Haemophilus Influenzae 41 7.958
325
GST019 Gastrointestinal Stromal Tumor 78 7.928
326
P SKN015 Skin Carcinoma 71 7.894
327
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 7.893
328
NRR001 Neuroretinitis 42 7.839
329
P THL005 Thalassemia 56 7.837
330
c LKM063 Leukemia, Chronic Myeloid 70 7.828
331
OTT002 Otitis Media 70 7.811
332
HYP080 Hypogonadism 49 7.802
333
P DYS154 Dystonia 64 7.782
334
ATM095 Autoimmune Disease 61 7.773
335
P GLM040 Glioma Susceptibility 1 70 7.764
336
P LNG064 Lung Cancer Susceptibility 3 69 7.720
337
STM007 Stomatitis 52 7.702
338
INT002 Intermittent Claudication 61 7.682
339
P APL001 Aplastic Anemia 72 7.682
340
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 7.675
341
GLM045 Glioma 62 7.660
342
CRN030 Coronary Stenosis 50 7.651
343
DBT010 Diabetic Neuropathy 54 7.621
344
PLM001 Pulmonary Tuberculosis 69 7.604
345
PRP080 Peripheral Artery Disease 54 7.601
346
P MYP006 Myopia 55 7.575
347
MCL006 Macular Retinal Edema 56 7.544
348
c SCL052 Scleroderma, Familial Progressive 60 7.524
349
BNR002 Bone Resorption Disease 47 7.512
350
P SCL018 Scoliosis 57 7.508
351
P HYP076 Hyperthyroidism 53 7.495
352
P RHB003 Rhabdomyosarcoma 66 7.471
353
c GLC092 Glaucoma, Primary Open Angle 60 7.466
354
RTN023 Retinitis 45 7.463
355
OVR094 Ovarian Epithelial Cancer 39 7.463
356
OBS002 Obsessive-Compulsive Disorder 67 7.444
357
MSC157 Muscular Dystrophy, Duchenne Type 78 7.426
358
c MCR112 Microvascular Complications of Diabetes 2 42 7.415
359
TTN003 Tetanus 64 7.343
360
P THY032 Thyroiditis 56 7.320
361
c ACT135 Acute Graft Versus Host Disease 51 7.312
362
CHL004 Cholelithiasis 48 7.305
363
PNC129 Pancreatic Adenocarcinoma 64 7.304
365
CRD132 Cardiac Conduction Defect 59 7.297
366
DFF005 Diffuse Large B-Cell Lymphoma 55 7.280
367
P HYD006 Hydrocephalus 62 7.277
368
NRL016 Neural Tube Defects 80 7.244
369
c INF071 Inflammatory Bowel Disease 1 65 7.238
370
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 7.222
371
PRT037 Pertussis 49 7.222
372
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 7.206
373
P HYP069 Hyperparathyroidism 62 7.188
374
P SYS005 Systemic Scleroderma 73 7.181
375
CRD223 Cardiac Arrhythmia 63 7.118
376
TRN015 Transient Cerebral Ischemia 62 7.078
377
ANR007 Anorexia Nervosa 59 7.065
378
TNS005 Tonsillitis 57 7.054
379
P TRM003 Tremor 50 7.045
380
KRT006 Keratoconjunctivitis 53 6.996
381
SXL003 Sexual Disorder 49 6.942
382
P RTN024 Retinoblastoma 72 6.923
383
P CYS018 Cystitis 58 6.913
384
c VRL010 Viral Hepatitis 52 6.912
385
DPH001 Diphtheria 59 6.909
386
P SLP005 Sleep Disorder 61 6.900
387
P PLY019 Polyneuropathy 52 6.884
388
SCK003 Sickle Cell Anemia 74 6.882
389
ACT084 Acute Stress Disorder 53 6.875
390
OCL006 Ocular Hypertension 53 6.870
391
P CHL066 Cholangitis 51 6.843
392
PRN019 Perinatal Necrotizing Enterocolitis 60 6.819
393
c HYP272 Hypercholesterolemia, Familial, 3 46 6.800
394
P NJM001 Nijmegen Breakage Syndrome 75 6.783
395
c BTT014 Beta-Thalassemia 72 6.771
396
LWC001 Low Compliance Bladder 44 6.759
397
RTN017 Retinal Detachment 60 6.739
398
CHL152 Childhood Acute Lymphocytic Leukemia 50 6.736
399
P PLY014 Polycystic Kidney Disease 71 6.708
400
CRH005 Crohn's Colitis 53 6.706
401
HYP005 Hypokalemia 55 6.687
402
VSC002 Vascular Dementia 59 6.669
403
KRT009 Keratosis 52 6.646
404
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 6.579
405
BRN056 Bronchopulmonary Dysplasia 57 6.577
406
P OVR082 Overgrowth Syndrome 41 6.575
407
GST040 Gastric Adenocarcinoma 66 6.571
408
c PRM038 Primary Agammaglobulinemia 47 6.550
409
INT066 Interstitial Lung Disease 60 6.542
410
P KDN017 Kidney Cancer 60 6.539
411
CHL065 Cholangiocarcinoma 57 6.538
412
P CCK001 Cockayne Syndrome 67 6.529
413
P UVT001 Uveitis 57 6.519
414
VGN023 Vaginitis 56 6.499
416
BLR008 Bilirubin Metabolic Disorder 57 6.481
417
ART002 Arts Syndrome 66 6.460
418
BRD004 Borderline Personality Disorder 53 6.422
419
P SNS001 Sensorineural Hearing Loss 60 6.421
420
VRC005 Varicose Veins 59 6.413
421
P NRV007 Nervous System Disease 65 6.411
422
RHM028 Rheumatic Heart Disease 55 6.393
423
PRT013 Portal Hypertension 59 6.291
424
GRW007 Growth Hormone Deficiency 47 6.278
425
LSH001 Leishmaniasis 63 6.278
426
P ART023 Arthropathy 59 6.275
427
HMC014 Homocysteinemia 52 6.252
428
HYP555 Hypertriglyceridemia, Transient Infantile 39 6.252
429
SBC016 Subacute Delirium 42 6.237
430
ENT004 Enthesopathy 51 6.229
431
AVD001 Avoidant Personality Disorder 49 6.210
432
P BND020 Bone Disease 60 6.204
433
P SRC025 Sarcoidosis 1 70 6.202
434
INT079 Intrahepatic Cholangiocarcinoma 51 6.200
435
P HYP730 Hypogonadotropic Hypogonadism 57 6.165
436
APP008 Appendicitis 62 6.158
437
P CHR071 Charcot-Marie-Tooth Disease 64 6.157
438
P HYP098 Hypereosinophilic Syndrome 66 6.138
439
P HRP006 Herpes Simplex 65 6.077
440
P SJG008 Sjogren Syndrome 60 6.063
441
AND005 Androgen Insensitivity Syndrome, Mild 21 6.055
442
AMN001 Amenorrhea 53 6.050
443
P BNG032 Benign Mesothelioma 53 6.028
444
APN008 Apnea, Obstructive Sleep 66 6.021
445
ATX019 Ataxia with Vitamin E Deficiency 44 6.018
446
KRT019 Keratitis, Hereditary 66 6.014
447
CNN005 Connective Tissue Disease 66 5.988
448
MLG169 Malignant Astrocytoma 57 5.981
449
P RRH023 Rare Hereditary Hemochromatosis 52 5.974
450
P CLC063 Celiac Disease 1 65 5.971
451
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 5.952
452
P KLZ004 Kala-Azar 1 41 5.947
453
MSL001 Measles 61 5.924
454
IGR001 Ige Responsiveness, Atopic 58 5.915
455
ALL006 Allergic Asthma 55 5.909
456
MSC007 Muscle Hypertrophy 64 5.903
457
LYM019 Lymphosarcoma 46 5.900
458
BRN002 Bronchiolitis 57 5.833
459
GNR004 Generalized Anxiety Disorder 54 5.828
460
LMY002 Leiomyoma 51 5.827
461
SCH012 Schizoaffective Disorder 49 5.823
462
c EXD008 Exudative Vitreoretinopathy 1 71 5.819
463
LYM027 Lymphopenia 56 5.815
464
HGH043 High Grade Glioma 46 5.808
465
P HML002 Hemolytic Anemia 62 5.796
466
ING001 Inguinal Hernia 59 5.784
467
HPT022 Hepatoblastoma 54 5.780
468
SCL003 Social Phobia 48 5.776
469
MRF001 Marfan Syndrome 76 5.773
470
SPL018 Splenomegaly 47 5.754
471
CRD137 Cardiogenic Shock 56 5.741
472
ILS001 Ileus 49 5.726
473
P TBR001 Tuberous Sclerosis 69 5.723
474
P ZLL001 Zellweger Syndrome 65 5.715
475
PST021 Postpartum Depression 50 5.703
476
VRL011 Viral Infectious Disease 60 5.697
477
TBC004 Tobacco Addiction 63 5.690
478
P MTR014 Motor Neuron Disease 65 5.675
479
IRN001 Iron Deficiency Anemia 58 5.667
480
PLM010 Pulmonary Edema 54 5.658
481
CHL067 Cholecystitis 59 5.647
482
P AMY004 Amyloidosis 69 5.635
483
LMB062 Limb Ischemia 55 5.627
484
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 5.619
485
PPT001 Peptic Esophagitis 51 5.596
486
P MLN007 Male Infertility 56 5.590
487
CLR108 Colorectal Adenoma 63 5.570
488
P PNC025 Panic Disorder 52 5.567
489
NPH009 Nephrolithiasis 54 5.565
490
THY030 Thyroid Gland Disease 50 5.560
491
MNN043 Meningioma, Familial 79 5.552
492
HMS001 Hemosiderosis 48 5.538
493
GTR002 Goiter 52 5.538
494
LYM040 Lymphoblastic Lymphoma 53 5.537
495
CLF027 Cleft Palate, Isolated 64 5.521
496
P SPP010 Suppressor of Tumorigenicity 3 50 5.503
497
SPT004 Septic Arthritis 58 5.487
498
P LMY004 Leiomyosarcoma 62 5.484
499
AST006 Astigmatism 46 5.484
500
DRY001 Dry Eye Syndrome 49 5.466
501
P ASP006 Aspergillosis 71 5.455
502
PLR007 Pleural Empyema 50 5.454
503
ART074 Aortic Dissection 53 5.447
504
MYL005 Myelofibrosis 70 5.447
505
P FML018 Familial Mediterranean Fever 73 5.445
506
DYS015 Dysentery 49 5.433
507
FCL014 Focal Epilepsy 53 5.414
508
WST001 West Syndrome 64 5.403
509
CMM005 Common Cold 55 5.391
510
P PHC003 Pheochromocytoma 70 5.387
511
BRT054 Brittle Bone Disorder 74 5.383
512
c JVN010 Juvenile Rheumatoid Arthritis 52 5.368
513
c INH020 Inherited Metabolic Disorder 47 5.361
514
P FLL037 Follicular Lymphoma 66 5.359
515
NRT004 Neuritis 53 5.355
516
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 5.352
517
TST014 Testicular Cancer 51 5.349
518
KRT001 Keratoconjunctivitis Sicca 49 5.325
519
P ERL057 Early Infantile Epileptic Encephalopathy 61 5.323
520
PRM236 Primary Biliary Cholangitis 62 5.322
521
c WLM013 Wilms Tumor 1 65 5.316
522
IGG001 Iga Glomerulonephritis 50 5.309
523
P OPT006 Optic Nerve Disease 57 5.289
524
MNT001 Mantle Cell Lymphoma 65 5.287
525
P GRV001 Graves' Disease 54 5.273
526
c HMP029 Hemophilia a 69 5.258
527
P ICH004 Ichthyosis 56 5.256
528
P BRN022 Bronchiectasis 59 5.234
529
PST092 Posttransplant Acute Limbic Encephalitis 29 5.216
530
P CRP001 Carpal Tunnel Syndrome 65 5.208
531
FDL002 Food Allergy 47 5.201
532
c BSL007 Basal Cell Carcinoma 67 5.195
533
FCT001 Factor Viii Deficiency 61 5.185
534
PPL022 Papilloma 53 5.168
535
PRP016 Paraplegia 52 5.165
536
HPT019 Hepatic Encephalopathy 59 5.160
537
SPN027 Spinal Stenosis 58 5.159
538
PNC001 Pancytopenia 52 5.134
539
c ACT134 Acute Liver Failure 57 5.124
540
ACR007 Acromegaly 70 5.081
541
P INT068 Intestinal Disease 53 5.065
542
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 5.057
543
c DRR009 Diarrhea 6 46 5.057
544
FRN006 Frontotemporal Dementia 68 5.053
545
P TXP001 Toxoplasmosis 59 5.047
546
SVR004 Severe Combined Immunodeficiency 70 5.046
547
PLC008 Placenta Disease 48 5.041
548
CRV045 Cervical Intraepithelial Neoplasia 38 5.022
549
P MCR010 Microcephaly 59 5.020
550
P LPR021 Leprosy 3 71 5.009
551
BRN028 Brain Cancer 73 5.009
552
PYR037 Pyruvate Carboxylase Deficiency 45 4.997
553
PRD004 Prediabetes Syndrome 52 4.994
554
DRM011 Dermatophytosis 52 4.993
555
ESP020 Esophageal Atresia 59 4.989
556
P HNT016 Huntington Disease 73 4.975
557
P MLG056 Malignant Hyperthermia 65 4.973
558
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 4.970
559
P HYP768 Hyperlipoproteinemia, Type I 67 4.966
560
ACT119 Acute Promyelocytic Leukemia 62 4.964
561
c PRG042 Progressive Familial Heart Block, Type Ia 65 4.962
562
c TBR026 Tuberous Sclerosis 2 71 4.962
563
P MMP001 Mumps 56 4.960
564
SQM002 Squamous Cell Papilloma 45 4.934
565
P RTN022 Retinal Vein Occlusion 54 4.929
566
RYN005 Raynaud Phenomenon 45 4.915
567
P MTR004 Maturity-Onset Diabetes of the Young 66 4.893
568
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 4.892
569
HPT004 Hepatic Coma 43 4.876
570
SYN036 Syncope 44 4.868
571
MYL031 Myeloproliferative Neoplasm 66 4.860
572
c PNC108 Pancreatitis, Hereditary 68 4.859
573
TLN003 Telangiectasis 51 4.855
574
P HMP007 Hemophilia 52 4.851
575
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 4.819
576
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 4.800
577
c MLT156 Multiple Endocrine Neoplasia, Type I 71 4.777
578
P ALP004 Alport Syndrome 69 4.761
579
GLL008 Gilles De La Tourette Syndrome 64 4.754
580
KPS004 Kaposi Sarcoma 76 4.742
581
P NNN008 Noonan Syndrome 1 76 4.740
582
FND002 Fundus Dystrophy 54 4.740
583
P RST001 Restless Legs Syndrome 52 4.733
584
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.732
585
HYP081 Hypolipoproteinemia 49 4.724
586
OHT001 Ohtahara Syndrome 39 4.700
587
LGH007 Leigh Syndrome 70 4.698
588
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 4.698
589
CRV002 Cervix Uteri Carcinoma in Situ 48 4.691
590
PHN003 Phenylketonuria 76 4.689
591
IDP070 Idiopathic Scoliosis 41 4.687
592
P NRF002 Neurofibromatosis 60 4.683
593
ATR057 Atrioventricular Block 54 4.679
594
P TTR001 Tetralogy of Fallot 69 4.669
595
P RBL001 Rubella 58 4.653
596
c ART101 Aortic Valve Disease 2 65 4.634
597
LBR036 Leber Plus Disease 67 4.599
598
P INT143 Interstitial Cystitis 59 4.589
599
P NRN021 Neuronal Ceroid Lipofuscinosis 64 4.586
600
P MVM001 Movement Disease 61 4.583
601
CRT016 Carotid Artery Disease 52 4.583
602
FBR012 Fabry Disease 71 4.578
603
GST050 Gastrointestinal System Disease 55 4.577
604
P KRT007 Keratoconus 49 4.565
605
KHN001 Kuhnt-Junius Degeneration 48 4.565
606
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 4.559
607
c HRD202 Hereditary Lymphedema I 54 4.556
608
OPT003 Opiate Dependence 49 4.556
609
STT001 Status Epilepticus 58 4.550
610
AYM001 Ayme-Gripp Syndrome 57 4.550
611
MYF002 Myofascial Pain Syndrome 46 4.541
612
P EPL140 Epilepsy, Idiopathic Generalized 60 4.541
613
ADR007 Adrenoleukodystrophy 73 4.533
614
BRS051 Breast Disease 58 4.529
615
SCH014 Schistosomiasis 56 4.524
616
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 4.523
617
P PLY018 Polycythemia 56 4.523
618
CMM004 Common Variable Immunodeficiency 71 4.515
619
P EMR001 Emery-Dreifuss Muscular Dystrophy 62 4.504
620
RDC002 Radiculopathy 51 4.500
621
OVR029 Ovarian Hyperstimulation Syndrome 63 4.499
622
P GND004 Gonadal Dysgenesis 46 4.497
623
P MSC003 Muscular Atrophy 52 4.487
624
P FML011 Familial Adenomatous Polyposis 70 4.484
625
TND005 Tendinitis 53 4.475
626
c CHR417 Chronic Graft Versus Host Disease 55 4.473
627
c ATM011 Autoimmune Hepatitis 62 4.455
628
EPT021 Epithelial Recurrent Erosion Dystrophy 45 4.438
629
NRM005 Neuromuscular Disease 62 4.429
630
NPH091 Nephrolithiasis, Calcium Oxalate 61 4.428
631
HMG005 Hemoglobinopathy 55 4.427
632
HMP005 Hemiplegia 53 4.423
633
c CNG012 Congenital Generalized Lipodystrophy 65 4.407
634
PRM013 Premature Menopause 57 4.405
635
P KHL003 Kohlschutter-Tonz Syndrome 57 4.370
636
P GCH001 Gaucher's Disease 69 4.368
637
EWN003 Ewing Sarcoma 69 4.356
638
SDD001 Sudden Infant Death Syndrome 60 4.352
639
c BPL002 Bipolar I Disorder 47 4.350
640
c HYP739 Hyperlipoproteinemia, Type Iv 53 4.337
641
EXC002 Exocrine Pancreatic Insufficiency 42 4.335
642
P BRD002 Bardet-Biedl Syndrome 66 4.327
643
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 4.299
644
P ATR010 Atrial Heart Septal Defect 58 4.291
645
FML026 Familial Lipoprotein Lipase Deficiency 51 4.281
646
WRN001 Werner Syndrome 69 4.267
647
P VNT002 Ventricular Septal Defect 58 4.259
648
P ACT008 Actinic Keratosis 53 4.252
649
P PTN014 Patent Ductus Arteriosus 1 59 4.252
650
RSC001 Rosacea 55 4.226
651
VSC003 Visceral Leishmaniasis 54 4.214
652
P MJR007 Major Affective Disorder 1 42 4.203
653
P TRT010 Teratoma 50 4.201
654
P TCD001 Tic Disorder 50 4.188
655
P PRC012 Pericardial Effusion 50 4.179
656
VSL002 Visual Epilepsy 39 4.172
657
c THY109 Thyroid Cancer, Nonmedullary, 1 55 4.167
658
PCK003 Pick Disease of Brain 70 4.167
659
PLS007 Plasmodium Falciparum Malaria 52 4.160
660
NRN004 Neuroendocrine Tumor 55 4.160
661
P THY023 Thymoma 64 4.156
662
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 4.145
663
P PMP001 Pemphigus 54 4.145
664
INS001 Insulinoma 59 4.136
665
LMY014 Leiomyoma, Uterine 55 4.135
666
THR100 Thrombocytopenic Purpura, Autoimmune 60 4.131
667
P LCH002 Lichen Planus 54 4.118
668
BTT017 Beta-Thalassemia Major 54 4.085
669
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.081
670
P THR005 Thrombotic Thrombocytopenic Purpura 64 4.070
671
P SPN052 Spondyloarthropathy 54 4.066
672
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 4.058
673
ERL001 Early Myoclonic Encephalopathy 62 4.057
674
FRZ001 Frozen Shoulder 54 4.055
675
P SCK002 Sick Sinus Syndrome 55 4.052
676
CLL010 Cellular Ependymoma 58 4.045
677
MYF001 Myofibroma 42 4.036
678
MLT157 Multiple System Atrophy 1 69 4.029
679
HYD002 Hydronephrosis 58 4.024
680
CRY008 Cryopyrin-Associated Periodic Syndrome 48 4.023
681
P MLT074 Multiple Endocrine Neoplasia 58 4.023
682
P ALP009 Alopecia Areata 59 4.016
683
PTH003 Pathologic Nystagmus 52 4.011
684
ATN005 Autonomic Dysfunction 45 4.011
685
MCL003 Macular Holes 44 3.997
686
P ANP001 Anaplastic Large Cell Lymphoma 59 3.996
687
MNN020 Meningococcal Infection 44 3.995
688
NSP002 Nasopharyngitis 45 3.994
689
c DPH024 Diaphragmatic Hernia, Congenital 63 3.989
690
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 3.979
691
DWR001 Dwarfism 44 3.977
692
BRR014 Barrett Esophagus 66 3.974
693
P CHR012 Chronic Granulomatous Disease 69 3.970
694
BRN012 Bronchiolitis Obliterans 56 3.960
695
P SML001 Small Cell Carcinoma 52 3.954
696
FCL012 Facial Paralysis 49 3.942
697
P PLV020 Pelvic Organ Prolapse 57 3.942
698
LYM017 Lyme Disease 63 3.937
699
CHR073 Choreatic Disease 53 3.932
700
PLY001 Polycythemia Vera 69 3.925
701
P MMB011 Membranous Nephropathy 50 3.922
702
PRM003 Premature Ejaculation 44 3.920
703
c ALP101 Alpha-Thalassemia 62 3.912
704
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 3.907
705
P RTN018 Retinal Disease 53 3.901
706
ACT011 Acute Contagious Conjunctivitis 41 3.895
707
PRS063 Paresthesia 39 3.891
708
P MTC069 Mitochondrial Disorders 57 3.888
709
PLL012 Pollen Allergy 44 3.881
710
CLN015 Colon Adenocarcinoma 64 3.871
711
WLS001 Wilson Disease 70 3.869
712
MCR013 Microphthalmia 59 3.866
713
P SCL057 Scoliosis, Isolated 1 40 3.861
714
c NMN015 Niemann-Pick Disease, Type C1 68 3.860
715
NRG002 Neurogenic Bladder 54 3.854
716
DRV001 Dravet Syndrome 69 3.854
717
P GLL018 Gallbladder Cancer 59 3.842
718
AGR002 Agoraphobia 45 3.840
719
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 3.839
720
c SCN036 Secondary Progressive Multiple Sclerosis 55 3.820
721
LNN001 Lennox-Gastaut Syndrome 61 3.817
722
SNS003 Sensory Peripheral Neuropathy 51 3.811
723
SCH003 Schizophreniform Disorder 54 3.802
724
P HYP265 Hypotonia 42 3.801
725
INV001 Invasive Aspergillosis 48 3.786
726
AMB002 Amblyopia 49 3.769
727
c HMC039 Hemochromatosis, Type 1 73 3.769
728
P SMK004 Smoking As a Quantitative Trait Locus 3 44 3.766
729
P HRD011 Hereditary Spherocytosis 63 3.765
730
CLR030 Clear Cell Renal Cell Carcinoma 53 3.764
731
P NMN002 Niemann-Pick Disease 60 3.762
732
RFR010 Refractory Anemia 49 3.757
733
P FRG001 Fragile X Syndrome 70 3.752
734
P MGR001 Migraine Without Aura 48 3.727
735
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 3.723
736
INT075 Intracranial Hypertension 52 3.718
737
PLV003 Pelvic Inflammatory Disease 54 3.717
738
RBS001 Rabies 57 3.717
739
P HYP024 Hypoparathyroidism 55 3.716
740
ESP002 Esophageal Varix 51 3.709
741
P LCT001 Lactic Acidosis 50 3.699
742
BCT021 Bacterial Sepsis 43 3.684
743
PRT038 Protein-Energy Malnutrition 53 3.671
744
HYP020 Hyperprolactinemia 63 3.671
745
c PRM005 Primary Hyperparathyroidism 59 3.666
746
DBT002 Diabetic Autonomic Neuropathy 40 3.648
747
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 3.646
748
VNH007 Von Hippel-Lindau Syndrome 72 3.636
749
P HMR005 Hemorrhoid 49 3.634
750
TRG002 Trigeminal Neuralgia 61 3.633
751
WTH001 Withdrawal Disorder 47 3.625
752
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 3.619
753
P VNW001 Von Willebrand's Disease 64 3.617
754
GRM005 Germ Cell Cancer 46 3.616
755
HST010 Histiocytosis 49 3.612
756
P MGR003 Migraine with Aura 51 3.603
757
P HMN010 Hemangioma 61 3.596
758
P CMP008 Compartment Syndrome 49 3.594
759
NRN005 Neuronal Ceroid-Lipofuscinoses 61 3.588
760
PRT082 Preterm Premature Rupture of the Membranes 56 3.585
761
ALP103 Alpha-1-Antitrypsin Deficiency 67 3.581
762
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 3.579
763
P RTT002 Rett Syndrome 79 3.569
764
PRP036 Peripheral T-Cell Lymphoma 52 3.565
765
TND004 Tendinopathy 45 3.555
766
P INT070 Intestinal Obstruction 57 3.554
767
GRN037 Granulomatosis with Polyangiitis 66 3.551
768
P ART018 Aortic Valve Insufficiency 52 3.546
769
P CRN037 Craniosynostosis 67 3.539
770
P FCL005 Focal Segmental Glomerulosclerosis 57 3.537
771
LPT006 Leptin Receptor Deficiency 50 3.537
772
ACT088 Acute Insulin Response 39 3.532
773
SPP007 Suppression Amblyopia 38 3.528
774
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 3.514
775
P LCT002 Lactose Intolerance 51 3.503
776
HND015 Hand Skill, Relative 29 3.495
777
P GLY013 Glycogen Storage Disease 59 3.495
778
c DWL002 Dowling-Degos Disease 1 58 3.491
779
P HMP002 Hemophagocytic Lymphohistiocytosis 60 3.487
780
c VSC019 Vesicoureteral Reflux 1 56 3.486
781
c ART115 Aortic Valve Disease 1 72 3.478
782
CRT084 Creatinine Clearance Quantitative Trait Locus 25 3.476
783
PST053 Postherpetic Neuralgia 39 3.474
784
FLL027 Fallopian Tube Carcinoma 66 3.467
785
THR004 Thrombocytosis 52 3.466
786
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 3.462
787
P ORT004 Orthostatic Intolerance 61 3.451
788
HML018 Homologous Wasting Disease 21 3.440
789
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 3.438
790
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 3.437
791
CRY035 Cryptorchidism, Unilateral or Bilateral 57 3.437
792
TNP001 Tinea Pedis 48 3.437
793
P MYM013 Moyamoya Disease 1 59 3.423
794
c HRD010 Hereditary Spastic Paraplegia 65 3.421
795
P TRT019 Torticollis 47 3.402
796
MDS022 Mediastinitis 47 3.401
797
HSH003 Hashimoto Thyroiditis 60 3.398
798
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 3.378
799
ANL018 Analbuminemia 53 3.359
800
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 3.355
801
P PTS002 Ptosis 52 3.354
802
CCN002 Cocaine Abuse 49 3.353
803
c PRG043 Progressive Familial Heart Block, Type Ib 54 3.346
804
CRC006 Carcinoid Syndrome 55 3.343
805
BP1002 Bap1 Tumor Predisposition Syndrome 42 3.342
806
P LFT003 Left Ventricular Noncompaction 58 3.341
807
END072 Endotheliitis 36 3.341
808
GST037 Gastroparesis 52 3.339
809
THY111 Thyroid Carcinoma, Familial Medullary 67 3.337
810
TNG002 Tangier Disease 63 3.337
811
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 3.334
812
LTN004 Late-Onset Retinal Degeneration 59 3.321
813
P VSC018 Visceral Steatosis 32 3.315
814
HMG002 Hemoglobinuria 50 3.313
815
PRM329 Premature Aging 36 3.312
816
CRV043 Cervical Dystonia 46 3.309
817
APH001 Aphthous Stomatitis 57 3.304
818
P FBR031 Febrile Seizures 52 3.298
819
MCR088 Microscopic Polyangiitis 51 3.292
820
c CNG006 Congenital Hypothyroidism 63 3.288
821
CYN002 Cyanosis, Transient Neonatal 43 3.286
822
KLD004 Keloid Disorder 38 3.279
823
ASP026 Asplenia, Isolated Congenital 43 3.277
824
PMP014 Pemphigoid 48 3.277
825
P MYT002 Myotonic Dystrophy 51 3.254
826
P BCK002 Beckwith-Wiedemann Syndrome 61 3.251
827
YLL002 Yellow Fever 61 3.249
828
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 48 3.249
829
HYP732 Hyperalphalipoproteinemia 1 53 3.244
830
OPD006 Opioid Addiction 48 3.243
831
PRT019 Protein-Losing Enteropathy 44 3.240
832
ANC002 Anca-Associated Vasculitis 44 3.235
833
P MYC033 Myoclonus 46 3.234
834
IRD001 Iridocyclitis 54 3.228
835
HTC003 Hutchinson-Gilford Progeria Syndrome 65 3.227
836
MTH009 Mouth Disease 57 3.227
837
P AGM001 Agammaglobulinemia 67 3.225
838
CCN001 Cocaine Dependence 47 3.211
839
AND014 Androgenic Alopecia 46 3.208
840
P CLS010 Cluster Headache 42 3.205
841
P PLM034 Pulmonary Emphysema 58 3.201
842
OPD001 Opioid Abuse 44 3.200
843
c ACT249 Acute Asthma 40 3.191
844
GLM044 Glomerular Disease 34 3.187
845
P LYM033 Lymphoproliferative Syndrome 59 3.179
846
ISL003 Isolated Growth Hormone Deficiency 56 3.178
847
BLR013 Biliary Tract Cancer 43 3.171
848
LWC002 Lowe Oculocerebrorenal Syndrome 68 3.167
849
VTM033 Vitamin K Deficiency Bleeding 49 3.159
850
c HYP839 Hyperlipidemia, Familial Combined, 1 30 3.158
851
TRC022 Tricuspid Valve Insufficiency 46 3.156
852
MSN001 Mesangial Proliferative Glomerulonephritis 44 3.151
853
CNT016 Central Retinal Vein Occlusion 53 3.141
854
LNG108 Langerhans Cell Histiocytosis 57 3.137
855
ACN002 Acanthosis Nigricans 56 3.129
856
CHR100 Chronic Ulcer of Skin 57 3.127
857
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 52 3.114
858
P DMN001 Diamond-Blackfan Anemia 73 3.113
859
P LRY019 Laryngitis 53 3.105
860
ACR008 Acrocallosal Syndrome 69 3.102
861
WLF001 Wolff-Parkinson-White Syndrome 63 3.102
862
P HYP055 Hypoplastic Left Heart Syndrome 65 3.101
863
P AGG001 Aggressive Periodontitis 55 3.083
864
c HMP004 Hemophilia B 68 3.079
865
DRG024 Drug Allergy 40 3.063
866
P RTN016 Retinal Degeneration 52 3.062
867
P HMC002 Homocystinuria 52 3.061
868
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 3.048
869
ADR016 Adrenal Cortical Carcinoma 61 3.044
870
LNG039 Lung Squamous Cell Carcinoma 57 3.043
871
SPP011 Suppression of Tumorigenicity 12 61 3.041
872
MYL020 Myelomeningocele 51 3.025
873
IDP091 Idiopathic Nephrotic Syndrome 49 3.024
874
ORL013 Oral Lichen Planus 45 3.024
875
c BRD010 Bardet-Biedl Syndrome 1 64 3.022
876
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 3.012
877
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 3.009
878
CHL013 Cholecystolithiasis 37 3.009
879
c SPR086 Spermatogenic Failure 3 47 3.004
880
HRL003 Hurler Syndrome 66 3.003
881
TRC008 Trachoma 53 3.002
882
P ALP061 Alopecia, Androgenetic, 1 48 3.002
883
RSP007 Respiratory Distress Syndrome, Infant 41 3.000
884
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 2.995
885
MCP033 Mucopolysaccharidoses 44 2.987
886
HYP017 Hypophosphatemia 49 2.984
887
DFF036 Differentiated Thyroid Carcinoma 51 2.980
888
P GLC113 Galactosemia I 65 2.975
889
P ANG015 Angioedema 56 2.967
890
P PLY006 Polydactyly 58 2.966
891
P NRC002 Narcolepsy 55 2.960
892
PNM010 Pneumothorax, Primary Spontaneous 58 2.960
893
P SPN046 Spinal Muscular Atrophy 62 2.953
894
SYS003 Systolic Heart Failure 49 2.950
895
CTS005 Catastrophic Antiphospholipid Syndrome 43 2.946
896
P OST001 Osteopetrosis 70 2.944
897
URN010 Urinary Tract Obstruction 55 2.939
898
P BRS044 Breast Adenocarcinoma 58 2.921
899
P MPL001 Maple Syrup Urine Disease 69 2.916
900
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 2.914
901
c CWD006 Cowden Syndrome 1 78 2.909
902
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 2.908
903
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 2.906
904
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 2.892
905
ACT058 Active Peptic Ulcer Disease 55 2.890
906
HYP781 Hypoascorbemia 52 2.888
907
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 2.885
908
SPN020 Spondylosis 46 2.879
909
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 2.879
910
CRB086 Cerebral Aneurysms 40 2.871
911
ERY003 Erythema Multiforme 56 2.854
912
c PSD047 Pseudo-Turner Syndrome 52 2.849
913
TRD006 Tardive Dyskinesia 53 2.848
914
CMB007 Combined Immunodeficiency 56 2.837
915
BCK003 Background Diabetic Retinopathy 46 2.836
916
VTM002 Vitamin B12 Deficiency 48 2.818
917
c HYD046 Hydatidiform Mole, Recurrent, 1 59 2.816
918
NNT017 Neonatal Adrenoleukodystrophy 51 2.808
919
PRN014 Paronychia 50 2.803
920
HRY003 Hairy Cell Leukemia 53 2.791
921
OST015 Osteochondrodysplasia 60 2.784
922
P HYP050 Hyperinsulinemic Hypoglycemia 56 2.783
923
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 2.782
924
P MTC003 Metachromatic Leukodystrophy 71 2.781
925
ALS001 Alstrom Syndrome 65 2.781
926
DDN006 Duodenitis 49 2.774
927
BLP005 Blepharitis 50 2.770
928
ADR022 Adrenomyeloneuropathy 38 2.765
929
c GLY060 Glycogen Storage Disease Ia 62 2.764
930
ADR054 Adrenocortical Carcinoma, Hereditary 47 2.764
931
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 2.760
932
CYS010 Cystinosis 61 2.760
933