Search results for PAC 1

1502 hits were found for PAC 1

# Family MCID Name MIFTS Score
1
HMN044 Human Immunodeficiency Virus Type 1 76 69.320
2
P ANR048 Aniridia 1 66 41.258
3
P DBT009 Diabetes Mellitus 67 34.449
4
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 34.254
5
IMM167 Immune Deficiency Disease 76 33.608
6
c AMY091 Amyotrophic Lateral Sclerosis 1 87 33.598
7
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 32.497
8
P HRP006 Herpes Simplex 65 30.477
9
c HYP836 Hypercholesterolemia, Familial, 1 73 30.063
10
c NRF024 Neurofibromatosis, Type I 76 29.753
12
P CRN300 Coronary Heart Disease 1 73 28.838
13
P GLM040 Glioma Susceptibility 1 70 28.627
14
c ATR087 Atrial Standstill 1 74 28.203
15
c PLM164 Pulmonary Hypertension, Primary, 1 75 27.521
16
c TBR025 Tuberous Sclerosis 1 84 27.177
17
c MLT156 Multiple Endocrine Neoplasia, Type I 71 26.584
18
c BRN108 Branchiootic Syndrome 1 63 26.542
19
P DRM053 Dermatitis, Atopic 65 26.374
20
c HMC039 Hemochromatosis, Type 1 73 26.182
21
INS024 Insulin-Like Growth Factor I 77 26.054
22
P ALZ034 Alzheimer Disease 87 26.028
23
c TYP009 Type 2 Diabetes Mellitus 91 25.796
24
c HYP595 Hypertension, Essential 84 25.638
25
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 25.631
26
P CLC063 Celiac Disease 1 65 25.593
27
P SRC025 Sarcoidosis 1 70 25.591
28
P JBR020 Joubert Syndrome 1 74 25.004
29
P LNG032 Lung Cancer 98 24.503
30
P NRF002 Neurofibromatosis 60 24.449
31
P BRS047 Breast Cancer 97 24.275
32
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 24.227
33
P PNC035 Pancreatic Cancer 87 24.220
34
P MYC007 Myocardial Infarction 69 24.106
35
P MCR129 Microvascular Complications of Diabetes 1 67 24.086
36
c OPT053 Optic Atrophy 1 62 23.744
37
c BRD010 Bardet-Biedl Syndrome 1 64 23.527
38
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 23.405
39
P GST053 Gastric Cancer 82 22.983
40
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 22.960
41
P LKM062 Leukemia, Acute Lymphoblastic 69 22.876
42
HYP056 Hypoglycemia 65 22.846
43
c SPN225 Spondyloarthropathy 1 70 22.621
44
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 22.605
45
c THY109 Thyroid Cancer, Nonmedullary, 1 55 22.577
46
c MGR028 Migraine with or Without Aura 1 63 22.302
47
RNL065 Renal Cell Carcinoma, Papillary, 1 79 22.268
48
P ADN016 Adenocarcinoma 63 22.150
49
P LKM002 Leukemia 65 22.137
50
HYP266 Hypoxia 56 21.950
51
LKC009 Leukocyte Adhesion Deficiency, Type I 69 21.945
52
P HRS035 Hirschsprung Disease 1 66 21.817
53
P KLZ004 Kala-Azar 1 41 21.814
54
c SML038 Small Cell Cancer of the Lung 68 21.657
55
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 21.631
56
c OVR114 Ovarian Cancer 1 60 21.574
57
c EPS039 Episodic Pain Syndrome, Familial, 1 42 21.554
58
c LBR004 Leber Congenital Amaurosis 1 53 21.475
59
CMP012 Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome 47 21.303
60
c HPT001 Hepatitis C 61 21.095
61
DWN001 Down Syndrome 70 20.977
62
P MLN008 Melanoma 75 20.692
63
P LYM118 Lymphoma 66 20.587
64
P OVR042 Ovarian Cancer 88 20.526
65
P HPT021 Hepatitis 68 20.524
66
CYT002 Cytokine Deficiency 43 20.352
67
48X005 48,xyyy 39 20.351
68
ISC004 Ischemia 61 20.291
69
c NPH019 Nephronophthisis 1 50 20.242
70
HYP066 Hyperglycemia 60 20.209
71
c AXN009 Axenfeld-Rieger Syndrome, Type 1 48 20.048
72
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 20.006
73
P MLT020 Multiple Sclerosis 79 19.738
74
P SCH015 Schizophrenia 74 19.694
75
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 19.633
76
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 19.470
77
P CLR023 Colorectal Cancer 100 19.326
78
LYN004 Lynch Syndrome I 60 19.324
79
DRM006 Dermatitis 61 19.288
80
c MYS033 Miyoshi Muscular Dystrophy 1 53 19.062
81
c RNG004 Ring Chromosome 1 32 18.880
82
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 53 18.866
83
c GLC092 Glaucoma, Primary Open Angle 60 18.809
84
RNL114 Renal Cell Carcinoma, Nonpapillary 79 18.784
85
P HPT023 Hepatocellular Carcinoma 95 18.623
86
GLB002 Glioblastoma 67 18.580
87
c GLL024 Gallbladder Disease 1 53 18.500
88
ACQ007 Acquired Immunodeficiency Syndrome 58 18.431
89
c LKM061 Leukemia, Acute Myeloid 83 18.416
90
P NRB001 Neuroblastoma 66 18.376
91
P SCL057 Scoliosis, Isolated 1 40 18.346
92
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 36 18.317
93
c PRS097 Prostate Cancer, Hereditary, 1 38 18.312
94
P PNC044 Pancreatitis 61 18.211
95
HMN014 Human Immunodeficiency Virus Infectious Disease 54 18.172
96
P MLT074 Multiple Endocrine Neoplasia 58 18.129
97
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 18.108
98
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 18.068
99
c SCH079 Schizophrenia 1 44 18.042
100
c DWL002 Dowling-Degos Disease 1 58 17.953
101
c NPH055 Nephrotic Syndrome, Type 1 52 17.784
102
P PRS040 Prostate Cancer 95 17.664
103
MYL069 Myeloma, Multiple 76 17.635
104
P MJR007 Major Affective Disorder 1 42 17.582
105
KNB006 Knobloch Syndrome 1 44 17.571
106
P NSP012 Nasopharyngeal Carcinoma 60 17.520
107
PLM129 Pulmonary Disease, Chronic Obstructive 74 17.480
108
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 17.445
109
c PNC106 Pancreatic Agenesis 1 51 17.421
110
SQM006 Squamous Cell Carcinoma 59 17.352
111
P KBK002 Kabuki Syndrome 1 66 17.286
112
AGN016 Aging 53 17.266
113
ATM095 Autoimmune Disease 61 17.188
114
P MYL006 Myeloid Leukemia 60 17.161
115
P NTR004 Neutropenia 62 16.945
116
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 16.902
117
P HRT032 Heart Disease 84 16.835
118
LPP008 Lipoprotein Quantitative Trait Locus 65 16.772
119
ATH013 Atherosclerosis Susceptibility 63 16.752
120
P BCL017 B-Cell Lymphoma 57 16.743
121
c HPT073 Hepatitis C Virus 70 16.736
122
GLM045 Glioma 62 16.723
123
P ALP061 Alopecia, Androgenetic, 1 48 16.677
124
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 16.668
125
P KDN018 Kidney Disease 71 16.656
126
P FRD001 Friedreich Ataxia 62 16.632
127
GLL048 Glial Tumor 51 16.599
128
c ACT027 Acute Pancreatitis 60 16.555
129
c PRC016 Pre-Eclampsia 64 16.481
130
P VND007 Van Der Woude Syndrome 1 60 16.474
131
c PLN017 Peeling Skin Syndrome 1 38 16.394
132
ART140 Arteries, Anomalies of 52 16.392
133
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 16.381
134
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 16.381
135
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 16.381
136
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 16.381
137
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 16.381
138
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 16.381
139
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 16.381
140
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 16.381
141
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 16.381
142
c VSC019 Vesicoureteral Reflux 1 56 16.300
143
STR067 Stroke, Ischemic 79 16.279
144
SVR001 Severe Acute Respiratory Syndrome 68 16.191
145
P LVR013 Liver Disease 68 16.072
146
LNG099 Lung Disease 62 15.968
147
P NRP001 Neuropathy 59 15.939
148
HLX001 Helix Syndrome 47 15.929
149
P CRB048 Cerebral Cavernous Malformations 63 15.915
150
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 31 15.915
151
RPD005 Rapidly Involuting Congenital Hemangioma 48 15.914
152
ANR007 Anorexia Nervosa 59 15.842
153
c MCR113 Microvascular Complications of Diabetes 3 52 15.817
154
P ART022 Arthritis 70 15.803
155
LYM133 Lymphoma, Hodgkin, Classic 69 15.614
156
P PTN014 Patent Ductus Arteriosus 1 59 15.585
157
P AST005 Asthma 75 15.569
158
c MCR120 Microvascular Complications of Diabetes 7 47 15.555
159
c USH036 Usher Syndrome, Type I 60 15.544
160
MYL009 Myelodysplastic Syndrome 67 15.474
161
c MCR133 Microvascular Complications of Diabetes 4 41 15.447
162
c MCR130 Microvascular Complications of Diabetes 6 41 15.437
163
P ATS364 Autism 72 15.427
164
P RHM011 Rheumatoid Arthritis 81 15.425
165
P PRD008 Periodontitis 63 15.423
166
TXC005 Toxic Shock Syndrome 61 15.415
167
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 15.412
168
P MJR001 Major Depressive Disorder 68 15.390
169
c HPT003 Hepatitis a 63 15.341
170
INT323 Intraocular Pressure Quantitative Trait Locus 63 15.274
171
c LKM005 Leukemia, T-Cell, Chronic 33 15.219
172
c MCR115 Microvascular Complications of Diabetes 5 65 15.212
173
c CHR684 Chronic Kidney Disease 73 15.206
174
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 53 15.047
175
CYS001 Cystic Fibrosis 77 14.989
176
PRT037 Pertussis 49 14.968
177
P PLM037 Pulmonary Hypertension 69 14.960
178
P DVL012 Developmental Dysplasia of the Hip 1 45 14.921
179
OST012 Osteoarthritis 77 14.918
180
ADL002 Adult Syndrome 69 14.917
181
OST159 Osteogenic Sarcoma 66 14.885
182
P VSC007 Vascular Disease 62 14.871
183
PRT251 Proteinuria, Chronic Benign 58 14.862
184
ESP021 Esophageal Cancer 84 14.817
185
PNC129 Pancreatic Adenocarcinoma 64 14.806
186
CHR619 Chromosome 2q35 Duplication Syndrome 64 14.655
187
P ADL017 Adult T-Cell Leukemia 53 14.648
188
MRF001 Marfan Syndrome 76 14.642
189
P LYN001 Lynch Syndrome 76 14.604
190
CNG034 Congestive Heart Failure 69 14.586
191
END057 Endometrial Cancer 76 14.479
192
P BLD134 Bladder Cancer 79 14.469
193
NNL005 Non-Alcoholic Fatty Liver Disease 63 14.428
194
LPT014 Leptin Deficiency or Dysfunction 77 14.403
195
LVR012 Liver Cirrhosis 62 14.384
196
P SPR120 Supranuclear Palsy, Progressive, 1 68 14.373
197
c ASP032 Asperger Syndrome 1 23 14.258
198
SPN035 Spindle Cell Sarcoma 51 14.209
199
END086 End Stage Renal Disease 54 14.207
200
CRV035 Cervical Cancer 72 14.163
201
47X002 47,xyy 47 14.160
202
c EXS019 Exostoses, Multiple, Type I 54 14.150
203
P RTN008 Retinitis Pigmentosa 79 14.128
204
P LKM071 Leukemia, Chronic Lymphocytic 74 14.127
205
P INF038 Influenza 68 14.065
206
P PHC003 Pheochromocytoma 70 13.998
207
CRH001 Crohn's Disease 80 13.925
208
P PLM174 Palmoplantar Keratoderma, Nonepidermolytic, Focal 1 42 13.868
209
SRC014 Sarcoma 64 13.856
210
P SZR006 Seizure Disorder 69 13.818
211
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 13.818
212
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 13.781
213
ALL029 Allergic Disease 61 13.770
214
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 13.750
215
P THR014 Thrombocytopenia 66 13.695
216
SVR004 Severe Combined Immunodeficiency 70 13.682
217
P ANP001 Anaplastic Large Cell Lymphoma 59 13.635
218
c HPT016 Hepatitis B 62 13.600
219
P TRN020 Turner Syndrome 67 13.552
220
P PLM036 Pulmonary Fibrosis 65 13.476
221
P STR020 Strabismus 56 13.475
222
c DNR003 Duane Retraction Syndrome 1 39 13.445
223
P EPL198 Epilepsy, Myoclonic Juvenile 61 13.433
224
P PRP019 Peripheral Nervous System Disease 57 13.431
225
ADN018 Adenoma 58 13.385
226
c ACT075 Acute Myocardial Infarction 55 13.378
227
P ADL010 Adult Respiratory Distress Syndrome 70 13.318
228
VCC001 Vaccinia 49 13.308
229
SKN019 Skin Melanoma 70 13.272
230
P PLV020 Pelvic Organ Prolapse 57 13.214
231
c HYP731 Hyperaldosteronism, Familial, Type I 59 13.212
232
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 13.190
233
CLT003 Colitis 63 13.158
234
P LPS004 Lupus Erythematosus 61 13.067
235
c SYS001 Systemic Lupus Erythematosus 85 13.041
236
P SLV027 Silver-Russell Syndrome 1 52 13.004
237
P OST002 Osteoporosis 76 12.945
238
PNC041 Pancreatic Ductal Adenocarcinoma 51 12.875
239
THY029 Thyroid Carcinoma 55 12.871
240
LYM143 Lymphoma, Non-Hodgkin, Familial 74 12.848
241
P PRK057 Parkinson Disease, Late-Onset 79 12.842
242
FTT001 Fatty Liver Disease 61 12.840
243
P LTR001 Lateral Sclerosis 57 12.828
244
P LNG064 Lung Cancer Susceptibility 3 69 12.818
245
P BPL003 Bipolar Disorder 56 12.813
246
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 12.812
247
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 12.812
248
P RTN024 Retinoblastoma 72 12.794
249
P GRF003 Graft-Versus-Host Disease 71 12.786
250
P ATR011 Atrial Fibrillation 66 12.766
251
LKC005 Leukocyte Adhesion Deficiency, Type Iii 50 12.692
252
c ACT068 Acute Cystitis 60 12.640
253
ULC004 Ulcerative Colitis 74 12.561
254
P DRR001 Diarrhea 55 12.508
255
LPD008 Lipid Metabolism Disorder 61 12.499
256
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 12.491
257
DFC004 Deficiency Anemia 74 12.484
258
SKN016 Skin Disease 63 12.484
259
ALC007 Alcohol Dependence 65 12.448
260
RHB024 Rhabdomyosarcoma 2 65 12.432
261
BNR002 Bone Resorption Disease 47 12.428
262
P PNM007 Pneumonia 64 12.415
263
P EPL164 Epilepsy 70 12.415
264
PRT036 Peritonitis 65 12.398
265
P TBR001 Tuberous Sclerosis 69 12.398
266
CNS004 Constipation 56 12.365
267
NRF007 Neurofibroma 63 12.341
268
P ENC004 Encephalitis 61 12.202
269
P RSP003 Respiratory Failure 73 12.201
270
MLR004 Malaria 77 12.192
271
P RHN004 Rhinitis 56 12.086
272
GLM014 Glomerulopathy with Fibronectin Deposits 1 20 12.043
273
P WSK001 Wiskott-Aldrich Syndrome 72 11.985
274
DPR016 Depression 64 11.973
275
P CTR002 Cataract 59 11.906
276
CRB039 Cerebrovascular Disease 65 11.891
277
BRN071 Brain Injury 50 11.879
278
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 11.865
279
P MYP004 Myopathy 67 11.838
280
MNT002 Mental Depression 56 11.817
281
P URN019 Urinary Tract Infection 48 11.808
282
P END044 Endometriosis 62 11.799
283
RCK004 Rickets 64 11.796
284
SPN186 Spinal Cord Injury 60 11.793
285
PNG002 Pain Agnosia 51 11.790
286
CVD001 Covid-19 59 11.772
287
P CRD119 Cardiac Arrest 68 11.705
288
P EPL140 Epilepsy, Idiopathic Generalized 60 11.676
289
STM007 Stomatitis 52 11.627
290
P GLN011 Glanzmann Thrombasthenia 1 66 11.625
291
BCT022 Bacterial Infectious Disease 55 11.620
292
ANR040 Aneurysm 60 11.603
293
P DMN002 Dementia 65 11.573
294
P MSC005 Muscular Dystrophy 66 11.559
295
TRM010 Traumatic Brain Injury 50 11.535
296
P KDN017 Kidney Cancer 60 11.499
297
P PRK039 Parkinsonism 55 11.468
298
P EXN002 Exanthem 58 11.374
299
P PLY014 Polycystic Kidney Disease 71 11.359
300
P HYP086 Hypothyroidism 68 11.353
301
GNT018 Gianotti Crosti Syndrome 23 11.331
302
c DPH024 Diaphragmatic Hernia, Congenital 63 11.298
303
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 11.279
304
HRW001 Hair Whorl 35 11.265
305
HGH043 High Grade Glioma 46 11.249
306
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 11.217
307
P SLP006 Sleep Apnea 69 11.180
308
INS001 Insulinoma 59 11.175
309
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 11.154
310
c BLD140 Blood Group, I System 47 11.148
311
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 11.135
312
c LKM063 Leukemia, Chronic Myeloid 70 11.112
313
P ENC018 Encephalopathy 62 11.111
314
CNT105 Central Core Disease of Muscle 59 11.078
315
P TMR010 Tumor Predisposition Syndrome 69 11.051
316
CHL065 Cholangiocarcinoma 57 11.046
317
P GLM007 Glomerulonephritis 59 11.045
318
P UNP013 Uniparental Disomy of Chromosome 1 22 11.034
319
c DLT002 Dilated Cardiomyopathy 79 11.010
320
ANX010 Anxiety 70 11.000
321
MLG169 Malignant Astrocytoma 57 10.983
322
MGL001 Megaloblastic Anemia 59 10.921
323
P INF032 Infertility 60 10.900
324
P OPN001 Open-Angle Glaucoma 55 10.890
325
P HYP069 Hyperparathyroidism 62 10.850
326
ALL003 Allergic Rhinitis 66 10.846
327
INT079 Intrahepatic Cholangiocarcinoma 51 10.834
328
PRS021 Prostatic Adenoma 43 10.822
329
P ALP008 Alopecia 53 10.809
330
PRS045 Prostatic Hypertrophy 53 10.795
331
c PRM005 Primary Hyperparathyroidism 59 10.768
332
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 10.765
333
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 27 10.748
334
P INF037 Inflammatory Bowel Disease 53 10.747
335
P ALC033 Alcohol Use Disorder 67 10.735
336
P CNJ013 Conjunctivitis 66 10.676
337
P BNG032 Benign Mesothelioma 53 10.643
338
PRS129 Prostatic Hyperplasia, Benign 48 10.632
339
RHB001 Rhabdoid Cancer 68 10.630
340
P DNG005 Dengue Virus 55 10.627
341
ANT039 Antisynthetase Syndrome 55 10.603
342
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 10.599
343
BRK010 Burkitt Lymphoma 65 10.549
344
APR006 Apert Syndrome 69 10.547
345
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 10.499
346
HYP060 Hyperinsulinism 53 10.481
347
SPP011 Suppression of Tumorigenicity 12 61 10.458
348
MCS002 Mucositis 55 10.410
349
P MYP006 Myopia 55 10.389
350
DNT012 Dental Caries 53 10.385
351
ART016 Aortic Aneurysm 68 10.356
352
P THY032 Thyroiditis 56 10.318
353
TTN003 Tetanus 64 10.300
354
P PLY011 Polycystic Ovary Syndrome 57 10.288
355
SFT003 Soft Tissue Sarcoma 43 10.244
356
LNG031 Lung Benign Neoplasm 51 10.244
357
KRT019 Keratitis, Hereditary 66 10.216
358
PRP027 Peripheral Vascular Disease 71 10.211
359
P BRN019 Bernard-Soulier Syndrome 61 10.195
360
P BND020 Bone Disease 60 10.170
361
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 10.157
362
SQM013 Squamous Cell Carcinoma, Head and Neck 75 10.149
363
CHL014 Cholera 62 10.115
364
THR024 Thrombosis 56 10.087
365
P VSC011 Vasculitis 61 10.086
366
P CRD246 Cardiovascular System Disease 55 10.070
367
OCL069 Ocular Motor Apraxia 57 10.057
368
ANG054 Angina Pectoris 65 10.056
369
MCL075 Macular Dystrophy, Corneal 55 10.031
370
ADR040 Adrenal Gland Pheochromocytoma 45 10.007
371
P ECL001 Eclampsia 52 9.977
372
BCK006 Back Pain 43 9.940
373
c SCL052 Scleroderma, Familial Progressive 60 9.924
374
P ATT013 Attention Deficit-Hyperactivity Disorder 65 9.917
375
P ATX030 Ataxia-Telangiectasia 80 9.835
376
c THR092 Thrombophilia Due to Thrombin Defect 74 9.800
377
KPS004 Kaposi Sarcoma 76 9.761
378
CRB004 Cerebral Artery Occlusion 45 9.659
379
P UVT001 Uveitis 57 9.649
380
P HMP007 Hemophilia 52 9.648
381
P CHR345 Chronic Pain 50 9.612
382
P RCT021 Rectum Cancer 54 9.604
383
PLM134 Pulmonary Fibrosis, Idiopathic 76 9.593
384
PRS047 Prostatitis 57 9.587
385
P MSC003 Muscular Atrophy 52 9.586
386
P SCL018 Scoliosis 57 9.584
387
INH023 Inherited Cancer-Predisposing Syndrome 53 9.558
388
OVR094 Ovarian Epithelial Cancer 39 9.536
389
OCL006 Ocular Hypertension 53 9.532
390
P MNN013 Meningitis 65 9.474
391
c PCH010 Pachyonychia Congenita 3 43 9.466
392
GST045 Gastroenteritis 58 9.447
393
P GST044 Gastritis 55 9.443
394
c PRG042 Progressive Familial Heart Block, Type Ia 65 9.443
395
c HRD202 Hereditary Lymphedema I 54 9.401
396
IMP005 Impotence 52 9.386
397
GST040 Gastric Adenocarcinoma 66 9.378
398
P ACN011 Acne 55 9.376
399
P HYD006 Hydrocephalus 62 9.364
400
GST019 Gastrointestinal Stromal Tumor 78 9.352
401
PST028 Post-Traumatic Stress Disorder 58 9.347
402
P HNT016 Huntington Disease 73 9.316
403
MSC007 Muscle Hypertrophy 64 9.310
405
DFF005 Diffuse Large B-Cell Lymphoma 55 9.302
406
NRR001 Neuroretinitis 42 9.284
407
P HYP098 Hypereosinophilic Syndrome 66 9.275
408
MNN043 Meningioma, Familial 79 9.268
409
TLN003 Telangiectasis 51 9.251
410
c HRD002 Hereditary Angioedema 61 9.229
411
NRN004 Neuroendocrine Tumor 55 9.219
412
P AMY004 Amyloidosis 69 9.218
413
GLB001 Gilbert Syndrome 53 9.204
414
PRP030 Purpura 54 9.191
415
P THL005 Thalassemia 56 9.184
416
P PRS038 Personality Disorder 65 9.182
417
MNT001 Mantle Cell Lymphoma 65 9.167
418
BRN024 Bronchitis 67 9.162
419
c ATS007 Autism Spectrum Disorder 71 9.148
420
c ACT071 Acute Kidney Failure 60 9.144
421
DSS008 Disease of Mental Health 74 9.104
422
P CND004 Candidiasis 57 9.100
423
RTN023 Retinitis 45 9.093
424
CHL123 Chlamydia 58 9.079
425
LSH001 Leishmaniasis 63 9.044
426
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 9.013
427
BRN028 Brain Cancer 73 9.008
428
PRP001 Propionic Acidemia 65 8.994
429
P HYP750 Hypertriglyceridemia, Familial 61 8.986
430
BRN002 Bronchiolitis 57 8.955
431
DYS073 Dysphagia 53 8.925
432
P FLL037 Follicular Lymphoma 66 8.900
433
PLM033 Pulmonary Embolism 58 8.869
434
GLC003 Glucose Intolerance 53 8.841
435
INT007 Intermediate Coronary Syndrome 53 8.837
436
LYM027 Lymphopenia 56 8.818
437
P HRD011 Hereditary Spherocytosis 63 8.817
438
P EYD002 Eye Disease 57 8.808
439
P SYS005 Systemic Scleroderma 73 8.778
440
P SCK005 Sickle Cell Disease 56 8.748
441
ORL015 Oral Squamous Cell Carcinoma 43 8.747
442
P SKN015 Skin Carcinoma 71 8.739
443
IRN002 Iron Metabolism Disease 56 8.736
444
c PRD040 Periodontitis, Chronic 52 8.706
445
RSC001 Rosacea 55 8.677
446
ORL011 Oral Cancer 60 8.672
447
c ACT073 Acute Leukemia 59 8.650
448
c PNS012 Paine Syndrome 60 8.622
449
ALL006 Allergic Asthma 55 8.610
450
c MJR022 Major Affective Disorder 8 37 8.610
451
c MJR024 Major Affective Disorder 9 40 8.610
452
ART002 Arts Syndrome 66 8.583
453
P NPH012 Nephrotic Syndrome 61 8.578
454
P SBS003 Substance Abuse 54 8.559
455
DNG003 Dengue Disease 65 8.543
456
P SNS001 Sensorineural Hearing Loss 60 8.535
457
PPL052 Papillomatosis, Confluent and Reticulated 34 8.532
458
c DRM054 Dermatitis, Atopic, 2 47 8.518
459
ETN001 Eating Disorder 59 8.517
460
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 8.492
461
P TRM003 Tremor 50 8.485
462
P SYP003 Syphilis 59 8.470
463
MSL001 Measles 61 8.467
464
KRT002 Keratomalacia 54 8.458
465
P ART021 Arteriosclerosis 53 8.403
466
P SPP010 Suppressor of Tumorigenicity 3 50 8.370
467
PPL022 Papilloma 53 8.358
468
GT001 Gout 63 8.352
469
P INS002 in Situ Carcinoma 52 8.321
470
P DYS154 Dystonia 64 8.311
471
DSS032 Disease by Infectious Agent 55 8.287
472
P MDL005 Medulloblastoma 75 8.285
473
P THY023 Thymoma 64 8.284
474
BRC012 Brucellosis 66 8.277
475
P HDC001 Headache 56 8.264
476
GST092 Gastroesophageal Reflux 59 8.234
477
HYP080 Hypogonadism 49 8.221
478
P FBR017 Fibrosarcoma 55 8.214
479
P CHR071 Charcot-Marie-Tooth Disease 64 8.200
480
PRT013 Portal Hypertension 59 8.195
481
CRB037 Cerebral Palsy 66 8.172
482
RTN017 Retinal Detachment 60 8.162
483
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 8.152
484
CRD132 Cardiac Conduction Defect 59 8.148
485
P RHB003 Rhabdomyosarcoma 66 8.142
486
NTR005 Nutritional Deficiency Disease 60 8.125
487
P LPR021 Leprosy 3 71 8.094
488
MDD011 Mood Disorder 61 8.076
489
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 8.075
490
HLC007 Helicobacter Pylori Infection 67 8.073
491
P HYP061 Hypertrophic Cardiomyopathy 68 8.069
492
CNN005 Connective Tissue Disease 66 8.028
493
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 67 8.024
494
IRR002 Irritable Bowel Syndrome 64 8.002
495
c THY107 Thymoma, Familial 42 7.981
496
SBC016 Subacute Delirium 42 7.965
497
HYP005 Hypokalemia 55 7.961
498
P ART023 Arthropathy 59 7.959
499
SQM002 Squamous Cell Papilloma 45 7.948
500
SPN051 Spondylitis 51 7.948
501
KRT009 Keratosis 52 7.942
502
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 34 7.883
503
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 7.881
504
c FML021 Familial Hypercholesterolemia 71 7.879
505
P BRN022 Bronchiectasis 59 7.878
506
PNM008 Pneumothorax 54 7.843
507
INT395 Intracranial Meningioma 47 7.838
508
PLM010 Pulmonary Edema 54 7.822
509
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 7.822
510
P GRV001 Graves' Disease 54 7.814
511
c MST023 Mesothelioma, Malignant 56 7.791
512
P HYP024 Hypoparathyroidism 55 7.783
513
BRN056 Bronchopulmonary Dysplasia 57 7.777
514
P SPN046 Spinal Muscular Atrophy 62 7.766
515
c FML001 Familial Atrial Fibrillation 65 7.765
516
SYN007 Synovitis 54 7.762
517
DPH001 Diphtheria 59 7.758
518
ATS010 Autosomal Recessive Disease 42 7.756
519
P LNG028 Long Qt Syndrome 63 7.756
520
INT066 Interstitial Lung Disease 60 7.747
521
P DST107 Distal Renal Tubular Acidosis 48 7.744
522
PLS009 Plasma Cell Neoplasm 64 7.709
523
DRM011 Dermatophytosis 52 7.699
524
P CHN012 Chondrosarcoma 56 7.696
525
P HYP076 Hyperthyroidism 53 7.696
526
MYL005 Myelofibrosis 70 7.658
527
OTT002 Otitis Media 70 7.654
528
c JVN010 Juvenile Rheumatoid Arthritis 52 7.635
529
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 7.627
530
P MYC008 Myocarditis 59 7.624
531
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 7.598
532
DWR001 Dwarfism 44 7.597
533
LMY002 Leiomyoma 51 7.588
534
PRP080 Peripheral Artery Disease 54 7.586
535
NLP001 Nail-Patella Syndrome 63 7.556
536
P OPT006 Optic Nerve Disease 57 7.554
537
NWC001 Newcastle Disease 47 7.543
538
P SLP005 Sleep Disorder 61 7.523
539
ATN004 Autonomic Neuropathy 42 7.512
540
TRN015 Transient Cerebral Ischemia 62 7.511
541
TRN018 Transitional Cell Carcinoma 56 7.507
542
HMP009 Haemophilus Influenzae 41 7.506
543
c MCR112 Microvascular Complications of Diabetes 2 42 7.487
544
P MLN069 Melanoma, Uveal 59 7.442
545
MLD018 Mild Cognitive Impairment 48 7.432
546
BRN004 Brain Edema 54 7.431
547
SCR001 Secretory Meningioma 40 7.423
548
P OVR082 Overgrowth Syndrome 41 7.399
549
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 7.393
550
c ACT135 Acute Graft Versus Host Disease 51 7.348
551
NPH009 Nephrolithiasis 54 7.337
552
CHG001 Chagas Disease 65 7.328
553
AST006 Astigmatism 46 7.323
554
CRD137 Cardiogenic Shock 56 7.298
555
P CHL066 Cholangitis 51 7.272
556
PPT005 Peptic Ulcer Disease 58 7.261
557
c VRL010 Viral Hepatitis 52 7.260
558
CLN015 Colon Adenocarcinoma 64 7.257
559
APP008 Appendicitis 62 7.252
560
c FNC043 Fanconi Anemia, Complementation Group E 62 7.251
561
IGR001 Ige Responsiveness, Atopic 58 7.247
562
HMN047 Human Cytomegalovirus Infection 59 7.228
563
PST092 Posttransplant Acute Limbic Encephalitis 29 7.222
564
RFR003 Refractive Error 41 7.220
565
c ATM024 Autoimmune Pancreatitis 52 7.195
566
HRT011 Heart Septal Defect 49 7.169
567
c FNC027 Fanconi Anemia, Complementation Group a 80 7.152
568
RLP002 Relapsing-Remitting Multiple Sclerosis 56 7.152
569
P END033 Endocarditis 58 7.111
570
FCH001 Fuchs' Endothelial Dystrophy 48 7.111
571
CHR178 Chromosomal Triplication 33 7.096
572
c ACT134 Acute Liver Failure 57 7.080
573
LYM002 Lymphoplasmacyte-Rich Meningioma 35 7.077
574
CHR222 Chromosome 1p36 Deletion Syndrome 48 7.074
575
INF009 Inflammatory Spondylopathy 30 7.065
576
OST003 Osteonecrosis 60 7.059
577
HNS001 Hansen's Disease 32 7.031
578
CNT047 Contact Dermatitis 56 7.007
579
AND005 Androgen Insensitivity Syndrome, Mild 21 6.969
580
NRL016 Neural Tube Defects 80 6.964
581
P MYS003 Myasthenia Gravis 67 6.949
582
P ASP006 Aspergillosis 71 6.940
583
P NRV007 Nervous System Disease 65 6.938
584
VRC005 Varicose Veins 59 6.935
585
HMZ003 Homozygous Familial Hypercholesterolemia 60 6.923
586
P HMN010 Hemangioma 61 6.896
587
P FML011 Familial Adenomatous Polyposis 70 6.890
588
MYL031 Myeloproliferative Neoplasm 66 6.877
589
ATN005 Autonomic Dysfunction 45 6.874
590
APN008 Apnea, Obstructive Sleep 66 6.864
591
ACT084 Acute Stress Disorder 53 6.853
592
INT002 Intermittent Claudication 61 6.849
593
P DDN001 Duodenal Ulcer 52 6.848
594
PTT037 Pituitary Tumors 44 6.844
595
SPL018 Splenomegaly 47 6.843
596
RNL077 Renal Fibrosis 46 6.841
597
OST017 Osteomyelitis 63 6.841
598
MTH009 Mouth Disease 57 6.838
599
STT001 Status Epilepticus 58 6.833
600
PSR001 Psoriatic Arthritis 61 6.828
601
ENT011 Enterocolitis 55 6.809
602
P RTT002 Rett Syndrome 79 6.801
603
P SMP003 Simpson-Golabi-Behmel Syndrome 49 6.797
604
BRR014 Barrett Esophagus 66 6.784
605
SYN036 Syncope 44 6.780
606
P APL001 Aplastic Anemia 72 6.776
607
FRN006 Frontotemporal Dementia 68 6.769
608
P FRG001 Fragile X Syndrome 70 6.760
609
PSY004 Psychotic Disorder 66 6.754
610
P PMP001 Pemphigus 54 6.744
611
CRN030 Coronary Stenosis 50 6.741
612
HRP004 Herpes Zoster 60 6.725
613
AVN001 Avian Influenza 61 6.715
614
BLR008 Bilirubin Metabolic Disorder 57 6.714
615
LYM040 Lymphoblastic Lymphoma 53 6.692
616
c BLD126 Bleeding Disorder, Platelet-Type, 18 39 6.684
617
c HYP724 Hyperlipoproteinemia, Type Iii 66 6.665
618
P MLN007 Male Infertility 56 6.661
619
SCH014 Schistosomiasis 56 6.632
620
CRD223 Cardiac Arrhythmia 63 6.627
621
PLC002 Plica Syndrome 35 6.613
622
P CYS018 Cystitis 58 6.608
623
KRT006 Keratoconjunctivitis 53 6.601
624
CLF027 Cleft Palate, Isolated 64 6.582
625
P HYP730 Hypogonadotropic Hypogonadism 57 6.567
626
CRV045 Cervical Intraepithelial Neoplasia 38 6.553
627
TTH006 Tooth Disease 51 6.551
628
P ANT006 Antiphospholipid Syndrome 55 6.547
629
P MVM001 Movement Disease 61 6.537
630
ANP005 Anaplastic Astrocytoma 59 6.535
631
MYC006 Mycosis Fungoides 64 6.526
632
MRK001 Merkel Cell Carcinoma 64 6.526
633
APH002 Aphasia 55 6.518
634
URM002 Uremia 47 6.510
635
P TMP001 Temporal Lobe Epilepsy 49 6.493
636
SNS003 Sensory Peripheral Neuropathy 51 6.486
637
ATR057 Atrioventricular Block 54 6.474
638
P ART005 Arteriovenous Malformation 64 6.461
639
INF034 Infective Endocarditis 53 6.447
640
NRL005 Neurilemmoma 60 6.445
641
PLY150 Polykaryocytosis Inducer 29 6.443
642
c SVR005 Severe Pre-Eclampsia 49 6.441
643
ACT119 Acute Promyelocytic Leukemia 62 6.438
644
ANX004 Anoxia 40 6.436
645
P RTN016 Retinal Degeneration 52 6.427
646
CRV002 Cervix Uteri Carcinoma in Situ 48 6.398
647
MCH006 Mechanical Strabismus 40 6.395
648
NRM005 Neuromuscular Disease 62 6.393
649
P HYP265 Hypotonia 42 6.381
650
AMN003 Amnestic Disorder 53 6.378
651
NWB001 Newborn Respiratory Distress Syndrome 56 6.378
652
c ART101 Aortic Valve Disease 2 65 6.348
653
AMN001 Amenorrhea 53 6.347
654
P TTR001 Tetralogy of Fallot 69 6.343
655
HDN002 Head Injury 44 6.342
656
HYP014 Hyperuricemia 51 6.342
657
LMB062 Limb Ischemia 55 6.332
658
MTR002 Mitral Valve Insufficiency 51 6.330
659
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 6.316
660
P GLL018 Gallbladder Cancer 59 6.315
661
P ANG015 Angioedema 56 6.311
662
ENT004 Enthesopathy 51 6.308
663
PRM024 Primary Angle-Closure Glaucoma 38 6.298
664
DGN001 Degenerative Disc Disease 48 6.288
665
ORL005 Oral Candidiasis 55 6.274
666
c BTT014 Beta-Thalassemia 72 6.270
667
HMT002 Hematologic Cancer 61 6.257
668
LWC001 Low Compliance Bladder 44 6.253
669
P VNT002 Ventricular Septal Defect 58 6.224
670
GTR002 Goiter 52 6.224
671
ADN011 Adenoid Cystic Carcinoma 68 6.224
673
PRT058 Pure Autonomic Failure 58 6.215
674
TND005 Tendinitis 53 6.208
675
P ESS003 Essential Thrombocythemia 68 6.203
676
APP015 Apparent Mineralocorticoid Excess 57 6.192
677
CLL003 Cellulitis 53 6.180
678
BRT054 Brittle Bone Disorder 74 6.177
679
PLS007 Plasmodium Falciparum Malaria 52 6.175
680
SPS057 Spasticity 43 6.158
681
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 6.151
682
GRW007 Growth Hormone Deficiency 47 6.151
683
P FML018 Familial Mediterranean Fever 73 6.140
684
P MCR010 Microcephaly 59 6.137
685
RSP019 Respiratory Distress Syndrome in Premature Infants 52 6.131
686
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 6.119
687
PLC008 Placenta Disease 48 6.107
688
DYS015 Dysentery 49 6.107
689
HYD002 Hydronephrosis 58 6.106
690
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 6.077
691
CHR074 Choriocarcinoma 46 6.076
692
c MLG084 Malignant Fibrous Histiocytoma 62 6.057
693
P RBL001 Rubella 58 6.029
694
P ALP009 Alopecia Areata 59 6.028
695
THY030 Thyroid Gland Disease 50 6.026
696
WST005 West Nile Virus 55 6.026
697
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 6.023
698
P CHR285 Chronic Myelomonocytic Leukemia 59 6.013
699
P HRD001 Hereditary Multiple Exostoses 48 5.955
700
SRC027 Sarcoma, Synovial 58 5.949
701
MLG079 Malignant Pleural Mesothelioma 42 5.938
702
FCL014 Focal Epilepsy 53 5.923
703
GST023 Gastric Ulcer 52 5.923
704
NPH091 Nephrolithiasis, Calcium Oxalate 61 5.917
705
PLL012 Pollen Allergy 44 5.908
706
PRG009 Progressive Multifocal Leukoencephalopathy 58 5.908
707
P PTS002 Ptosis 52 5.899
708
CNN003 Conn's Syndrome 77 5.887
709
P BRS044 Breast Adenocarcinoma 58 5.885
710
P PYL005 Pyelonephritis 56 5.866
711
PHR003 Pharyngitis 57 5.865
712
MTB004 Metabolic Acidosis 48 5.853
713
c SCN007 Secondary Hyperparathyroidism 50 5.830
714
XRD010 Xeroderma Pigmentosum, Variant Type 72 5.830
715
P SML001 Small Cell Carcinoma 52 5.818
716
P CMP008 Compartment Syndrome 49 5.814
717
P GLL022 Guillain-Barre Syndrome 59 5.811
718
NSP002 Nasopharyngitis 45 5.803
719
GST050 Gastrointestinal System Disease 55 5.785
720
P LYM033 Lymphoproliferative Syndrome 59 5.771
721
PRC013 Pericarditis 53 5.769
722
CRC006 Carcinoid Syndrome 55 5.764
723
HPT022 Hepatoblastoma 54 5.745
724
JPN002 Japanese Encephalitis 61 5.741
725
CMM005 Common Cold 55 5.731
726
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 5.724
727
SXL003 Sexual Disorder 49 5.723
728
RDC002 Radiculopathy 51 5.716
729
THY111 Thyroid Carcinoma, Familial Medullary 67 5.709
730
c TBR026 Tuberous Sclerosis 2 71 5.709
731
ADR016 Adrenal Cortical Carcinoma 61 5.708
732
P PRG013 Paraganglioma 57 5.703
733
CRT013 Carotid Stenosis 51 5.694
734
P LPS002 Liposarcoma 64 5.684
735
P LMY004 Leiomyosarcoma 62 5.663
736
INT075 Intracranial Hypertension 52 5.637
737
c LKM056 Leukemia, Chronic Lymphocytic 2 47 5.627
738
P USH001 Usher Syndrome 63 5.613
739
c CNT035 Central Nervous System Disease 53 5.612
740
URT010 Ureteral Obstruction 44 5.606
741
CLR109 Colorectal Adenocarcinoma 50 5.597
742
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 5.595
743
HRT012 Heart Valve Disease 53 5.566
744
ART074 Aortic Dissection 53 5.564
745
GST037 Gastroparesis 52 5.556
746
P HRM001 Hermansky-Pudlak Syndrome 65 5.555
747
P INT068 Intestinal Disease 53 5.527
748
END041 Endometrial Adenocarcinoma 63 5.525
749
DSS009 Disseminated Intravascular Coagulation 56 5.517
750
GLS001 Gliosarcoma 63 5.493
751
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 5.453
752
NRN001 Neuroendocrine Carcinoma 47 5.449
753
c CHR417 Chronic Graft Versus Host Disease 55 5.438
754
VSC002 Vascular Dementia 59 5.436
755
MLG077 Malignant Peripheral Nerve Sheath Tumor 53 5.421
756
P NPH005 Nephronophthisis 59 5.411
757
DCT002 Ductal Carcinoma in Situ 58 5.410
758
LPM012 Lipomatosis, Multiple 59 5.400
759
PPL002 Papillary Carcinoma 46 5.399
760
OBS002 Obsessive-Compulsive Disorder 67 5.383
761
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 5.383
762
c BRS111 Breast-Ovarian Cancer, Familial 2 53 5.378
763
THR004 Thrombocytosis 52 5.370
764
ADR054 Adrenocortical Carcinoma, Hereditary 47 5.364
765
PRM013 Premature Menopause 57 5.363
766
P SYR001 Syringomyelia 46 5.359
767
SYR010 Syringomyelia, Noncommunicating Isolated 36 5.357
768
ALV005 Alveolar Soft Part Sarcoma 61 5.350
769
P OBS001 Obstructive Jaundice 49 5.328
770
P BLD062 Bile Duct Cancer 69 5.325
771
INT030 Intracranial Aneurysm 55 5.322
772
P DBT005 Diabetes Insipidus 54 5.316
773
P EPD016 Epidermolysis Bullosa 53 5.305
774
LMY014 Leiomyoma, Uterine 55 5.303
775
CLF004 Cleft Lip/palate 56 5.303
776
ILS001 Ileus 49 5.299
777
CRC014 Carcinoid Tumors, Intestinal 46 5.280
778
HMP005 Hemiplegia 53 5.265
779
SPN019 Spondylolisthesis 51 5.264
780
PMP006 Pemphigus Vulgaris, Familial 57 5.257
781
TST014 Testicular Cancer 51 5.254
782
RYN005 Raynaud Phenomenon 45 5.251
783
CLF001 Cleft Lip 54 5.250
784
SDD001 Sudden Infant Death Syndrome 60 5.243
785
P EXD001 Exudative Vitreoretinopathy 56 5.231
786
THR100 Thrombocytopenic Purpura, Autoimmune 60 5.223
787
P HMR003 Hemorrhagic Disease 59 5.213
788
c DNT047 Dentinogenesis Imperfecta Type 2 35 5.213
789
BLP005 Blepharitis 50 5.209
790
NRN005 Neuronal Ceroid-Lipofuscinoses 61 5.205
791
LYM021 Lymphadenitis 55 5.196
792
ANT024 Anthrax Disease 57 5.196
793
PLR008 Pleurisy 49 5.192
794
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 5.190
795
IDP070 Idiopathic Scoliosis 41 5.157
796
GRN037 Granulomatosis with Polyangiitis 66 5.150
797
HMC014 Homocysteinemia 52 5.131
798
c BLD152 Bleeding Disorder, Platelet-Type, 16 35 5.129
799
c HMP004 Hemophilia B 68 5.128
800
P CRN026 Corneal Edema 42 5.085
801
P RNV001 Renovascular Hypertension 48 5.080
802
P NRN021 Neuronal Ceroid Lipofuscinosis 64 5.077
803
YLL002 Yellow Fever 61 5.073
804
P PRD006 Prader-Willi Syndrome 60 5.062
805
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 5.026
806
ANG020 Angiosarcoma 63 5.013
807
PLG002 Plague 58 5.009
808
ACT003 Acute Kidney Tubular Necrosis 46 5.000
809
CHR072 Chordoma 56 4.986
810
P KRT007 Keratoconus 49 4.979
811
P INT070 Intestinal Obstruction 57 4.965
812
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 4.964
813
GST071 Gastrointestinal Carcinoma 46 4.963
814
P MLG056 Malignant Hyperthermia 65 4.951
815
P PRM011 Primary Ciliary Dyskinesia 68 4.951
816
c BCT007 Bacterial Meningitis 55 4.941
817
VLV047 Volvulus of Midgut 55 4.940
818
PNN001 Panniculitis 52 4.922
819
CTN007 Cutaneous Leishmaniasis 61 4.891
820
RFR010 Refractory Anemia 49 4.884
821
P RTN022 Retinal Vein Occlusion 54 4.882
822
P ANG001 Angelman Syndrome 64 4.877
823
SPP007 Suppression Amblyopia 38 4.872
824
AMB002 Amblyopia 49 4.872
825
SPN027 Spinal Stenosis 58 4.865
826
P CHR342 Chiari Malformation 41 4.846
827
HDR003 Hidradenitis 49 4.844
828
P ATR005 Atrophic Gastritis 50 4.829
829
ERL001 Early Myoclonic Encephalopathy 62 4.814
830
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 4.810
831
P BCK002 Beckwith-Wiedemann Syndrome 61 4.808
832
MDD018 Middle East Respiratory Syndrome 44 4.807
833
ADR007 Adrenoleukodystrophy 73 4.792
834
TND004 Tendinopathy 45 4.786
835
ADR004 Adrenal Cortical Adenocarcinoma 38 4.784
836
ISL001 Islet Cell Tumor 55 4.779
837
HPT019 Hepatic Encephalopathy 59 4.766
838
BRN012 Bronchiolitis Obliterans 56 4.759
839
HDR002 Hidradenitis Suppurativa 54 4.749
840
P LRY044 Larynx Cancer 53 4.742
841
P SBR004 Seborrheic Dermatitis 44 4.740
842
c DRR009 Diarrhea 6 46 4.731
843
ALL009 Allergic Conjunctivitis 51 4.721
844
HPT004 Hepatic Coma 43 4.718
845
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 4.717
846
P THR015 Thrombophilia 51 4.712
847
P ORT004 Orthostatic Intolerance 61 4.710
848
MNN009 Meningoencephalitis 47 4.706
849
CHL067 Cholecystitis 59 4.704
850
WRN001 Werner Syndrome 69 4.701
851
CYS009 Cystadenoma 42 4.697
852
DGR001 Digeorge Syndrome 62 4.697
853
NRG002 Neurogenic Bladder 54 4.688
854
ALL010 Allergic Contact Dermatitis 55 4.683
855
OPT003 Opiate Dependence 49 4.681
856
CHL004 Cholelithiasis 48 4.678
857
c ALB021 Albinism, Oculocutaneous, Type Ii 58 4.675
858
LRN003 Learning Disability 49 4.659
859
PYD002 Pyoderma 49 4.656
860
RSP007 Respiratory Distress Syndrome, Infant 41 4.651
861
SYS003 Systolic Heart Failure 49 4.642
862
WLL001 Williams-Beuren Syndrome 60 4.634
863
P RRT020 Rare Tumor 39 4.627
864
GST012 Gastroesophageal Junction Adenocarcinoma 46 4.609
865
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 4.607
866
P CLS010 Cluster Headache 42 4.591
867
DCB001 Decubitus Ulcer 61 4.576
868
c 46X049 46,xy Sex Reversal 2 51 4.556
869
BLM002 Bulimia Nervosa 56 4.532
870
PLP001 Pulpitis 48 4.528
871
SMT008 Smith-Magenis Syndrome 53 4.522
872
QDR001 Quadriplegia 49 4.519
873
c BCT013 Bacterial Pneumonia 47 4.514
874
FLL027 Fallopian Tube Carcinoma 66 4.509
875
AZS001 Azoospermia 45 4.509
876
ARG004 Argyria 26 4.507
877
PYD001 Pyoderma Gangrenosum 53 4.496
878
MCR011 Microinvasive Gastric Cancer 41 4.468
879
OCL022 Ocular Melanoma 54 4.461
880
IRN001 Iron Deficiency Anemia 58 4.455
881
P MTR003 Mitral Valve Stenosis 53 4.448
882
P THR005 Thrombotic Thrombocytopenic Purpura 64 4.429
883
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 57 4.412
884
PNM010 Pneumothorax, Primary Spontaneous 58 4.409
885
P CRN037 Craniosynostosis 67 4.404
886
PRS025 Presbyopia 39 4.402
887
P ATR010 Atrial Heart Septal Defect 58 4.381
888
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.367
889
P LCT001 Lactic Acidosis 50 4.365
890
HRY003 Hairy Cell Leukemia 53 4.340
891
ACH005 Achalasia 54 4.338
892
APP009 Appendix Adenocarcinoma 47 4.337
893
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 4.337
894
P PRC012 Pericardial Effusion 50 4.325
895
SCH074 Schuurs-Hoeijmakers Syndrome 48 4.322
896
CYN002 Cyanosis, Transient Neonatal 43 4.320
897
KRT008 Keratopathy 46 4.312
898
HYP017 Hypophosphatemia 49 4.311
899
HMP001 Hemopericardium 47 4.307
900
CHD004 Chudley-Mccullough Syndrome 47 4.302
901
EXF001 Exfoliation Syndrome 55 4.294
902
P SHR001 Short Bowel Syndrome 53 4.289
903
MTH071 Methane Production 24 4.279
904
P HYP040 Hypospadias 51 4.279
905
BCT004 Bacteriuria 48 4.273
906
THY022 Thymic Carcinoma 56 4.272
907
MMB001 Membranoproliferative Glomerulonephritis 56 4.271
908
P MST009 Mastocytosis 64 4.268
909
P CRC039 Coarctation of Aorta 46 4.251
910
GLM044 Glomerular Disease 34 4.249
911
P ECT006 Ectodermal Dysplasia 62 4.246
912
RST023 Resting Heart Rate, Variation in 40 4.244
913
CNT016 Central Retinal Vein Occlusion 53 4.233
914
c PRG043 Progressive Familial Heart Block, Type Ib 54 4.232
915
PNC034 Pancreas Disease 49 4.231
916
THY125 Thyroid Gland Medullary Carcinoma 48 4.227
917
GRM010 Germ Cells Tumors 33 4.226
918
APR001 Apraxia 51 4.221
919
P CNG010 Congenital Stationary Night Blindness 56 4.216
920
CHR103 Charge Syndrome 65 4.215
921
MRG003 Marginal Zone B-Cell Lymphoma 52 4.204
922
P EPD009 Epidermolysis Bullosa Dystrophica 66 4.202
923
INT051 Intussusception 53 4.201
924
ACS001 Acoustic Neuroma 55 4.197
925
CHR177 Chromophobe Renal Cell Carcinoma 54 4.191
926
P CYS039 Cystic Kidney Disease 52 4.185
927
ACT058 Active Peptic Ulcer Disease 55 4.175
928
SRS001 Serous Cystadenocarcinoma 51 4.174
929
P FBR003 Fibrous Histiocytoma 43 4.156
930
OST015 Osteochondrodysplasia 60 4.150
931
c PRM093 Premature Ovarian Failure 7 47 4.145
932
CCC001 Coccidioidomycosis 57 4.140
933
P HYP083 Hypopituitarism 51 4.132
934
MCR088 Microscopic Polyangiitis 51 4.129
935
PRT010 Parathyroid Carcinoma 68 4.102
936
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 4.083
937
WLF002 Wolf-Hirschhorn Syndrome 57 4.070
938
ILT001 Ileitis 49 4.068
939
PYR004 Pyuria 36 4.067
940
BTT017 Beta-Thalassemia Major 54 4.064
941
INT146 Intervertebral Disc Disease 61 4.059
942
ONC007 Oncocytoma 49 4.037
943
MXD005 Mixed Connective Tissue Disease 57 4.031
944
P AGG001 Aggressive Periodontitis 55 4.021
945
P TCD001 Tic Disorder 50 4.020
946
PLM005 Pleomorphic Lipoma 39 4.013