Search results for cs

2974 hits were found for cs

# Family MCID Name MIFTS Score
1
P HRT032 Heart Disease 84 18.459
2
c TYP009 Type 2 Diabetes Mellitus 92 17.454
3
c CWD006 Cowden Syndrome 1 79 17.403
4
P CCK001 Cockayne Syndrome 68 15.831
5
P CWD010 Cowden Syndrome 71 15.653
6
c DLT002 Dilated Cardiomyopathy 79 13.200
7
P MYP004 Myopathy 67 12.922
8
c AMY091 Amyotrophic Lateral Sclerosis 1 88 11.921
9
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 11.516
10
P HYP061 Hypertrophic Cardiomyopathy 69 11.171
11
CRZ001 Crouzon Syndrome 64 11.009
12
c XRD022 Xeroderma Pigmentosum, Complementation Group D 56 10.715
13
c XRD023 Xeroderma Pigmentosum, Complementation Group G 53 10.674
14
NRM005 Neuromuscular Disease 63 10.530
15
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 10.232
16
P GLY013 Glycogen Storage Disease 59 10.088
17
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 34 10.078
18
SNL007 Senile Cataract 40 10.045
19
EPD015 Epidemic Typhus 44 9.939
20
c XRD032 Xeroderma Pigmentosum, Complementation Group B 49 9.645
21
c XRD031 Xeroderma Pigmentosum, Complementation Group F 55 9.617
22
ACT245 Acth-Dependent Cushing Syndrome 23 8.976
23
NRR001 Neuroretinitis 42 7.635
24
SPT005 Spotted Fever 49 7.180
25
P MTC069 Mitochondrial Disorders 57 7.180
26
c INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 26 7.116
27
CTS002 Cat-Scratch Disease 42 7.103
28
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 7.016
29
LGH007 Leigh Syndrome 70 6.987
30
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 6.987
31
P MTC133 Mitochondrial Myopathy 51 6.987
32
JPN001 Japanese Spotted Fever 21 6.916
33
RCK002 Rocky Mountain Spotted Fever 34 6.916
34
CNZ010 Coenzyme Q10 Deficiency, Primary, 7 41 6.916
35
END014 Endemic Typhus 32 6.916
36
MTC079 Mitochondrial Pyruvate Carrier Deficiency 29 6.916
37
QNS001 Queensland Tick Typhus 21 6.916
38
CRR001 Carrion's Disease 31 6.916
39
BCL011 Bacillary Angiomatosis 29 6.916
40
c MTC059 Mitochondrial Dna Depletion Syndrome 5 48 6.916
41
c SPS100 Spastic Paraplegia 38, Autosomal Dominant 37 6.916
42
BRT043 Bartonellosis 35 6.916
43
BTN002 Boutonneuse Fever 42 6.916
44
CRT009 Critical Illness Polyneuropathy 35 6.916
45
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 6.916
46
PDC003 Pediculus Humanus Corporis Infestation 22 6.916
47
PLM129 Pulmonary Disease, Chronic Obstructive 74 5.955
48
CRD137 Cardiogenic Shock 56 5.856
49
c HYP595 Hypertension, Essential 84 4.859
50
HRW001 Hair Whorl 35 4.731
51
MLR004 Malaria 78 4.492
52
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.467
53
P SRC025 Sarcoidosis 1 70 4.367
54
CRD003 Cardiac Sarcoidosis 44 4.277
55
P LNG032 Lung Cancer 98 3.993
56
P INF038 Influenza 68 3.906
57
P CLR023 Colorectal Cancer 100 3.855
58
CNN003 Conn's Syndrome 77 3.758
59
OST012 Osteoarthritis 77 3.653
60
LNG099 Lung Disease 62 3.648
61
c SML038 Small Cell Cancer of the Lung 69 3.636
62
XRD010 Xeroderma Pigmentosum, Variant Type 72 3.526
63
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.467
64
P MYC007 Myocardial Infarction 69 3.440
65
c MCR115 Microvascular Complications of Diabetes 5 65 3.430
66
48X005 48,xyyy 39 3.411
67
ISC004 Ischemia 61 3.400
68
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 3.290
69
P ART023 Arthropathy 60 3.271
70
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.258
71
P PNC035 Pancreatic Cancer 86 3.211
72
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 3.145
73
c ACT068 Acute Cystitis 61 3.134
74
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.091
75
P PRS040 Prostate Cancer 95 3.088
76
c MCR133 Microvascular Complications of Diabetes 4 41 3.080
77
c MCR113 Microvascular Complications of Diabetes 3 52 3.080
78
c MCR130 Microvascular Complications of Diabetes 6 41 3.080
79
c MCR120 Microvascular Complications of Diabetes 7 47 3.080
80
P URN019 Urinary Tract Infection 49 3.060
81
c HYP836 Hypercholesterolemia, Familial, 1 73 2.993
82
ATH013 Atherosclerosis Susceptibility 63 2.983
83
P BRS047 Breast Cancer 97 2.978
84
P MLT020 Multiple Sclerosis 79 2.959
85
PLC009 Placenta Praevia 39 2.866
86
P DBT009 Diabetes Mellitus 67 2.829
87
ART140 Arteries, Anomalies of 52 2.810
88
LPP008 Lipoprotein Quantitative Trait Locus 65 2.799
89
c ACT075 Acute Myocardial Infarction 55 2.792
90
PRT251 Proteinuria, Chronic Benign 58 2.674
91
CST001 Costello Syndrome 68 2.671
92
BCT022 Bacterial Infectious Disease 56 2.640
93
CRC021 Carcinosarcoma 62 2.640
94
P THL005 Thalassemia 56 2.624
95
P SYP003 Syphilis 59 2.531
96
c CNG033 Congenital Syphilis 39 2.496
97
HMP009 Haemophilus Influenzae 41 2.495
98
P CHN012 Chondrosarcoma 56 2.482
99
MYL069 Myeloma, Multiple 77 2.462
100
CNG034 Congestive Heart Failure 69 2.457
101
P TRN020 Turner Syndrome 67 2.444
102
c CCK008 Cockayne Syndrome a 59 2.438
103
P ART022 Arthritis 70 2.416
104
c THR092 Thrombophilia Due to Thrombin Defect 74 2.352
105
PST028 Post-Traumatic Stress Disorder 59 2.294
106
HYP066 Hyperglycemia 60 2.289
107
VCC001 Vaccinia 49 2.230
108
c MCR112 Microvascular Complications of Diabetes 2 42 2.222
109
P MCR129 Microvascular Complications of Diabetes 1 68 2.222
110
THY029 Thyroid Carcinoma 54 2.216
111
47X002 47,xyy 48 2.200
112
P KDN018 Kidney Disease 72 2.193
113
P CRD119 Cardiac Arrest 68 2.187
114
P CHR345 Chronic Pain 50 2.185
115
P CYS018 Cystitis 59 2.183
116
P LYM118 Lymphoma 69 2.175
117
CNT047 Contact Dermatitis 57 2.166
118
P CRN300 Coronary Heart Disease 1 73 2.163
119
P ATR011 Atrial Fibrillation 66 2.159
120
ALC007 Alcohol Dependence 65 2.153
121
ATS010 Autosomal Recessive Disease 42 2.134
122
PLS007 Plasmodium Falciparum Malaria 52 2.125
123
P GLM007 Glomerulonephritis 59 2.107
124
c BLD140 Blood Group, I System 47 2.086
125
CHR174 Christianson Syndrome 47 2.083
126
ALL029 Allergic Disease 61 2.081
127
HLX001 Helix Syndrome 47 2.059
128
c PRM038 Primary Agammaglobulinemia 47 2.001
129
c FML021 Familial Hypercholesterolemia 71 2.001
130
c ATR087 Atrial Standstill 1 74 2.000
131
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.984
132
CLT003 Colitis 63 1.955
133
ULC004 Ulcerative Colitis 74 1.929
134
PLM010 Pulmonary Edema 54 1.923
135
ANX010 Anxiety 70 1.920
136
c PRC016 Pre-Eclampsia 64 1.915
137
P CTR002 Cataract 59 1.903
138
P THY032 Thyroiditis 56 1.897
139
BRN024 Bronchitis 67 1.895
140
ADN018 Adenoma 58 1.889
141
PLM033 Pulmonary Embolism 58 1.865
142
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.835
143
HYP060 Hyperinsulinism 53 1.828
144
P SCH015 Schizophrenia 74 1.827
145
ALL014 Allergic Encephalomyelitis 34 1.823
146
SPN020 Spondylosis 46 1.823
147
P RHN004 Rhinitis 57 1.822
148
TTN003 Tetanus 64 1.819
149
SPN392 Spondylosis, Cervical 30 1.817
150
SVR004 Severe Combined Immunodeficiency 71 1.816
151
PNG002 Pain Agnosia 51 1.810
152
CRH001 Crohn's Disease 80 1.810
153
TRC096 Trichothiodystrophy 56 1.809
154
END086 End Stage Renal Disease 54 1.799
155
VRL011 Viral Infectious Disease 60 1.789
156
AST006 Astigmatism 46 1.788
157
P HPT023 Hepatocellular Carcinoma 95 1.781
158
P SCL018 Scoliosis 57 1.773
159
STR067 Stroke, Ischemic 79 1.773
160
P OVR042 Ovarian Cancer 88 1.772
161
BCK006 Back Pain 43 1.772
162
P NTR004 Neutropenia 62 1.765
163
ALL003 Allergic Rhinitis 66 1.762
164
CRT013 Carotid Stenosis 51 1.758
165
P RHM011 Rheumatoid Arthritis 81 1.752
166
P BCL017 B-Cell Lymphoma 57 1.751
167
MTH071 Methane Production 25 1.748
168
UTR024 Uterine Carcinosarcoma 58 1.748
169
P SKN015 Skin Carcinoma 71 1.747
170
GLB002 Glioblastoma 67 1.741
171
PLM001 Pulmonary Tuberculosis 69 1.740
172
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.738
173
AGN016 Aging 54 1.735
174
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.733
175
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.733
176
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.733
177
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.733
178
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.733
179
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.733
180
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.733
181
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.733
182
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.733
183
P AST005 Asthma 76 1.732
184
ALL010 Allergic Contact Dermatitis 56 1.718
185
LPD008 Lipid Metabolism Disorder 61 1.718
186
P ANR048 Aniridia 1 66 1.706
187
P HYP098 Hypereosinophilic Syndrome 66 1.695
188
P VSC011 Vasculitis 61 1.683
189
AMB002 Amblyopia 49 1.682
190
SPP007 Suppression Amblyopia 38 1.682
191
CYT002 Cytokine Deficiency 43 1.677
192
P SLP006 Sleep Apnea 69 1.662
193
P ALZ034 Alzheimer Disease 87 1.662
194
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.649
195
P CRB101 Cerebrooculofacioskeletal Syndrome 1 52 1.644
196
P MYC084 Mycobacterium Tuberculosis 1 68 1.637
197
THR024 Thrombosis 56 1.637
198
GLL048 Glial Tumor 52 1.636
199
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.633
200
GLM045 Glioma 62 1.630
201
PRT037 Pertussis 49 1.627
202
CRD132 Cardiac Conduction Defect 59 1.623
203
LNG031 Lung Benign Neoplasm 51 1.606
204
P PRD008 Periodontitis 64 1.594
205
SPN186 Spinal Cord Injury 61 1.589
206
AMN003 Amnestic Disorder 54 1.589
207
BNR002 Bone Resorption Disease 47 1.536
208
OST062 Osteoarthritis with Mild Chondrodysplasia 47 1.529
209
ACT084 Acute Stress Disorder 53 1.529
210
P ADL010 Adult Respiratory Distress Syndrome 71 1.504
211
c ALP101 Alpha-Thalassemia 62 1.499
212
OST159 Osteogenic Sarcoma 66 1.494
214
P CNJ013 Conjunctivitis 66 1.481
215
END057 Endometrial Cancer 71 1.474
216
DFF005 Diffuse Large B-Cell Lymphoma 55 1.447
217
c HPT016 Hepatitis B 62 1.443
218
P CRN037 Craniosynostosis 67 1.439
219
P CMP008 Compartment Syndrome 50 1.430
220
P ADN016 Adenocarcinoma 63 1.429
221
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.421
222
GLC003 Glucose Intolerance 53 1.416
223
c MCP049 Mucopolysaccharidosis, Type Vii 62 1.410
224
ATM095 Autoimmune Disease 61 1.401
225
c ACT071 Acute Kidney Failure 60 1.398
226
LYM019 Lymphosarcoma 46 1.396
227
P LTR001 Lateral Sclerosis 58 1.387
228
P HRP006 Herpes Simplex 65 1.384
229
P VSC007 Vascular Disease 62 1.370
230
PRM329 Premature Aging 36 1.368
231
P BLP003 Blepharospasm 45 1.364
232
ANR040 Aneurysm 60 1.353
233
P NRP001 Neuropathy 59 1.347
234
P PTT006 Pituitary Adenoma 55 1.346
235
HYP266 Hypoxia 56 1.344
236
P CND004 Candidiasis 57 1.339
237
DWN001 Down Syndrome 70 1.327
238
TNS014 Tenosynovitis 45 1.327
239
P MYC008 Myocarditis 59 1.326
240
P DMN002 Dementia 65 1.320
241
P THR014 Thrombocytopenia 66 1.320
242
P PNC044 Pancreatitis 61 1.315
243
PRT036 Peritonitis 65 1.314
244
SMT007 Smith-Fineman-Myers Syndrome 32 1.314
245
GST033 Gestational Diabetes 61 1.312
246
RHB024 Rhabdomyosarcoma 2 65 1.312
247
ADR008 Adrenal Adenoma 55 1.309
248
AVN001 Avian Influenza 61 1.307
249
PTN001 Patent Foramen Ovale 62 1.307
250
c CHR684 Chronic Kidney Disease 74 1.305
251
P HYP750 Hypertriglyceridemia, Familial 62 1.303
252
P CRD246 Cardiovascular System Disease 55 1.300
253
TST014 Testicular Cancer 51 1.296
254
DRM006 Dermatitis 62 1.293
255
PRP030 Purpura 54 1.293
256
WLF001 Wolff-Parkinson-White Syndrome 63 1.290
257
c BTT014 Beta-Thalassemia 72 1.290
258
P HDC001 Headache 56 1.290
259
ART016 Aortic Aneurysm 69 1.286
260
c MGR028 Migraine with or Without Aura 1 64 1.283
261
CRN030 Coronary Stenosis 50 1.282
262
MLD018 Mild Cognitive Impairment 48 1.277
263
OCL069 Ocular Motor Apraxia 57 1.272
264
SMN007 Seminoma 42 1.271
265
c ACT027 Acute Pancreatitis 60 1.270
266
P CLD003 Cold-Induced Sweating Syndrome 40 1.265
267
SYN007 Synovitis 54 1.264
268
PLC002 Plica Syndrome 35 1.264
269
MTR002 Mitral Valve Insufficiency 51 1.262
270
HYP056 Hypoglycemia 65 1.258
271
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.252
272
RTN017 Retinal Detachment 60 1.248
273
P PRP019 Peripheral Nervous System Disease 57 1.247
274
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 1.245
275
ATR057 Atrioventricular Block 54 1.244
276
c SPN330 Spondylocostal Dysostosis 5 55 1.244
277
TLN003 Telangiectasis 51 1.235
278
STH001 Saethre-Chotzen Syndrome 66 1.225
279
P PLM034 Pulmonary Emphysema 58 1.220
280
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.219
281
CRC006 Carcinoid Syndrome 55 1.218
282
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 1.214
283
P ASP006 Aspergillosis 71 1.214
284
SRC014 Sarcoma 64 1.214
285
CRV035 Cervical Cancer 72 1.211
286
P SJG008 Sjogren Syndrome 61 1.208
287
P HPT021 Hepatitis 68 1.204
288
c CCK007 Cockayne Syndrome B 56 1.200
289
P SYS005 Systemic Scleroderma 73 1.200
290
ALL006 Allergic Asthma 56 1.197
292
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.187
293
CLR109 Colorectal Adenocarcinoma 50 1.184
294
SPN035 Spindle Cell Sarcoma 51 1.184
295
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.182
296
MDD018 Middle East Respiratory Syndrome 44 1.179
297
HMN044 Human Immunodeficiency Virus Type 1 76 1.171
298
OST017 Osteomyelitis 63 1.171
299
P TRM003 Tremor 50 1.171
300
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.171
301
P ATX030 Ataxia-Telangiectasia 80 1.164
302
SVR001 Severe Acute Respiratory Syndrome 68 1.164
303
OST016 Osteochondrosis 52 1.162
304
P PLM036 Pulmonary Fibrosis 65 1.153
305
CYS001 Cystic Fibrosis 77 1.153
306
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.152
307
CRT017 Cartilage Disease 52 1.152
308
P VNW001 Von Willebrand's Disease 64 1.149
309
OST022 Osteopathia Striata with Cranial Sclerosis 54 1.130
310
SPL018 Splenomegaly 47 1.126
311
P HMG032 Hemoglobin H Disease 51 1.124
312
P HYP086 Hypothyroidism 69 1.122
313
HSH003 Hashimoto Thyroiditis 60 1.122
314
HMG005 Hemoglobinopathy 55 1.122
315
P ALC033 Alcohol Use Disorder 67 1.119
316
P SPP010 Suppressor of Tumorigenicity 3 51 1.118
317
PPL052 Papillomatosis, Confluent and Reticulated 34 1.118
318
P MYP006 Myopia 55 1.114
319
RTR001 Retrograde Amnesia 41 1.112
320
c HPT001 Hepatitis C 61 1.110
321
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 1.106
322
P PYL005 Pyelonephritis 56 1.106
323
P ART021 Arteriosclerosis 53 1.104
325
PLS009 Plasma Cell Neoplasm 64 1.103
326
BRN014 Bronchopneumonia 52 1.103
327
IFP003 Ifap Syndrome 2 42 1.102
328
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 1.098
329
P MCR010 Microcephaly 59 1.098
330
P PLY019 Polyneuropathy 53 1.098
331
c HPT073 Hepatitis C Virus 71 1.093
332
CRB091 Cerebro-Oculo-Facio-Skeletal Syndrome 34 1.093
333
P NRB001 Neuroblastoma 66 1.091
334
ABD010 Abdominal Wall Defect 39 1.089
335
CVD001 Covid-19 58 1.085
336
LYM133 Lymphoma, Hodgkin, Classic 74 1.084
337
P ECL001 Eclampsia 52 1.082
338
HRT011 Heart Septal Defect 49 1.082
339
BLC012 Bile Acid Malabsorption, Primary 43 1.081
340
CHL014 Cholera 62 1.081
341
P LKM002 Leukemia 66 1.077
342
PLC001 Placenta Accreta 44 1.075
343
TXC005 Toxic Shock Syndrome 62 1.075
344
P RHB003 Rhabdomyosarcoma 66 1.072
345
ILS001 Ileus 49 1.068
346
TND005 Tendinitis 54 1.068
347
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.066
348
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.066
349
P GST053 Gastric Cancer 82 1.064
350
P NPH012 Nephrotic Syndrome 62 1.064
351
FRY002 Fryns Syndrome 39 1.060
352
STN013 Stenotrophomonas Maltophilia Infection 26 1.060
353
GST092 Gastroesophageal Reflux 60 1.059
354
P OST002 Osteoporosis 77 1.057
355
PRS045 Prostatic Hypertrophy 52 1.055
356
P BRS044 Breast Adenocarcinoma 58 1.055
357
P RTN024 Retinoblastoma 72 1.053
358
PRS129 Prostatic Hyperplasia, Benign 48 1.050
359
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.050
360
P INF037 Inflammatory Bowel Disease 53 1.047
361
PLY150 Polykaryocytosis Inducer 29 1.046
362
INF034 Infective Endocarditis 53 1.037
363
P TMP003 Temporal Arteritis 68 1.036
364
P PLM037 Pulmonary Hypertension 69 1.035
365
P UVT001 Uveitis 57 1.033
366
P LPS004 Lupus Erythematosus 61 1.033
367
c CRS017 Crisponi/cold-Induced Sweating Syndrome 2 34 1.031
368
HMT002 Hematologic Cancer 61 1.031
369
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.026
370
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.023
371
PRS021 Prostatic Adenoma 43 1.023
372
SCB001 Scabies 49 1.018
373
PLS006 Plasmodium Vivax Malaria 51 1.014
374
P RSP003 Respiratory Failure 74 1.011
375
P MYL006 Myeloid Leukemia 60 1.009
376
LYM143 Lymphoma, Non-Hodgkin, Familial 79 1.008
377
c NYS017 Nystagmus 1, Congenital, X-Linked 29 1.008
378
c CNG618 Congenital Nystagmus 1 16 1.008
379
P PRK039 Parkinsonism 55 1.004
380
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.004
381
P OPT006 Optic Nerve Disease 57 1.004
382
TST043 Testicular Seminoma 31 1.004
383
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.001
384
DMP001 Dumping Syndrome 43 1.000
385
P TXP001 Toxoplasmosis 60 0.999
386
P END046 Endometritis 46 0.996
387
P PRS038 Personality Disorder 65 0.990
388
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.989
389
GST009 Gastroschisis 53 0.989
390
BRN002 Bronchiolitis 57 0.989
391
PRS063 Paresthesia 39 0.989
392
P INF032 Infertility 60 0.979
393
IDP070 Idiopathic Scoliosis 41 0.976
394
P SCK002 Sick Sinus Syndrome 55 0.973
395
TND004 Tendinopathy 45 0.972
396
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.965
397
P LRY044 Larynx Cancer 53 0.965
398
P SZR006 Seizure Disorder 69 0.963
399
c LKM061 Leukemia, Acute Myeloid 83 0.963
400
c INF071 Inflammatory Bowel Disease 1 65 0.962
401
c OVR114 Ovarian Cancer 1 60 0.962
402
URN022 Urinary Tract Infections, Recurrent 27 0.962
403
AND005 Androgen Insensitivity Syndrome, Mild 21 0.962
404
P OST009 Osteochondritis Dissecans 61 0.962
405
IDP069 Idiopathic Avascular Necrosis 23 0.962
406
P OPN001 Open-Angle Glaucoma 55 0.958
407
CRR002 Currarino Syndrome 49 0.958
408
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.956
409
c SYS001 Systemic Lupus Erythematosus 86 0.956
410
P ESP024 Esophagitis 60 0.952
411
P GLL018 Gallbladder Cancer 53 0.952
412
OCL006 Ocular Hypertension 53 0.952
413
c GLL024 Gallbladder Disease 1 53 0.941
414
SBC016 Subacute Delirium 42 0.941
415
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.937
416
P INS002 in Situ Carcinoma 53 0.937
417
P LNG028 Long Qt Syndrome 63 0.936
418
P BNG032 Benign Mesothelioma 53 0.936
419
LYM021 Lymphadenitis 56 0.935
420
DWR001 Dwarfism 45 0.932
421
AMN001 Amenorrhea 53 0.931
422
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.929
423
HYP005 Hypokalemia 55 0.929
424
FDL002 Food Allergy 47 0.924
425
BLR008 Bilirubin Metabolic Disorder 57 0.924
426
P ALP008 Alopecia 53 0.924
427
DPR016 Depression 65 0.924
428
DNT012 Dental Caries 53 0.921
429
ADR016 Adrenal Cortical Carcinoma 61 0.919
430
SDD001 Sudden Infant Death Syndrome 60 0.918
431
CRB039 Cerebrovascular Disease 65 0.916
432
INT007 Intermediate Coronary Syndrome 53 0.916
433
ANT039 Antisynthetase Syndrome 55 0.916
434
APN008 Apnea, Obstructive Sleep 66 0.916
435
P BLD134 Bladder Cancer 79 0.913
436
RFR003 Refractive Error 41 0.913
437
P EYD002 Eye Disease 57 0.910
438
PRC013 Pericarditis 53 0.906
439
P DRM053 Dermatitis, Atopic 65 0.905
440
KRT019 Keratitis, Hereditary 66 0.905
441
OVR044 Ovarian Carcinosarcoma 46 0.904
442
INT002 Intermittent Claudication 61 0.902
443
BLD053 Blood Platelet Disease 51 0.900
444
c NYS005 Nystagmus 4, Congenital, Autosomal Dominant 32 0.900
445
P TMR010 Tumor Predisposition Syndrome 69 0.899
446
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.899
447
INH023 Inherited Cancer-Predisposing Syndrome 53 0.899
448
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.894
449
VSC002 Vascular Dementia 59 0.894
450
c BRN108 Branchiootic Syndrome 1 63 0.894
451
PRS047 Prostatitis 58 0.893
452
P MTR014 Motor Neuron Disease 65 0.892
453
OCL052 Ocular Dominance 40 0.888
454
CHL004 Cholelithiasis 48 0.888
455
c VRL010 Viral Hepatitis 52 0.887
456
OTT002 Otitis Media 71 0.887
457
P MLN069 Melanoma, Uveal 59 0.882
458
P SNS001 Sensorineural Hearing Loss 59 0.880
459
MNN043 Meningioma, Familial 79 0.877
460
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.877
461
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.875
462
c BSL007 Basal Cell Carcinoma 68 0.875
463
NRW001 Norwegian Scabies 36 0.875
464
P DRR001 Diarrhea 55 0.874
465
c NYS004 Nystagmus 3, Congenital, Autosomal Dominant 24 0.874
466
c NYS003 Nystagmus 2, Congenital, Autosomal Dominant 31 0.874
467
c NYS012 Nystagmus 5, Congenital, X-Linked 24 0.874
468
INT395 Intracranial Meningioma 48 0.871
469
SYN036 Syncope 44 0.871
470
SCR001 Secretory Meningioma 40 0.871
471
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.871
472
FRZ001 Frozen Shoulder 54 0.868
473
DMY004 Demyelinating Disease 50 0.868
474
CGN006 Cogan Syndrome 49 0.863
475
P BNC003 Bone Cancer 58 0.862
476
CHR048 Chronic Rhinitis 46 0.862
477
ORL011 Oral Cancer 60 0.860
478
CHD004 Chudley-Mccullough Syndrome 47 0.857
479
P KLZ004 Kala-Azar 1 41 0.857
480
LSH001 Leishmaniasis 63 0.857
481
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.855
482
BRS064 Bursitis 51 0.855
483
OCL022 Ocular Melanoma 54 0.855
484
ANG054 Angina Pectoris 65 0.854
485
ADR040 Adrenal Gland Pheochromocytoma 45 0.851
486
P PHC003 Pheochromocytoma 70 0.851
487
c SCL052 Scleroderma, Familial Progressive 60 0.851
488
P PNM007 Pneumonia 64 0.851
489
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.848
490
SKN016 Skin Disease 62 0.848
491
ADR004 Adrenal Cortical Adenocarcinoma 38 0.848
492
P OVR082 Overgrowth Syndrome 42 0.848
493
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.848
494
NPH009 Nephrolithiasis 54 0.848
495
P CRB088 Cerebral Atrophy 33 0.848
496
RVL002 Ruvalcaba Syndrome 42 0.842
497
FBR047 Fibromyalgia 58 0.842
498
SNT005 Sinoatrial Node Disease 47 0.841
499
ORP003 Oropharynx Cancer 54 0.841
500
PRP027 Peripheral Vascular Disease 71 0.837
501
TRN015 Transient Cerebral Ischemia 62 0.834
502
CNS004 Constipation 56 0.834
503
P ENC018 Encephalopathy 62 0.834
504
PPT001 Peptic Esophagitis 51 0.834
505
YLL002 Yellow Fever 61 0.834
506
LFT001 Left Bundle Branch Hemiblock 47 0.831
507
EXP004 Exophthalmos 50 0.828
508
THY030 Thyroid Gland Disease 50 0.827
509
LMB062 Limb Ischemia 55 0.819
510
c CRB099 Cerebrooculofacioskeletal Syndrome 3 32 0.819
511
P ANP001 Anaplastic Large Cell Lymphoma 61 0.819
512
ALV001 Alveolar Periostitis 34 0.819
513
MCL003 Macular Holes 44 0.819
514
SFT003 Soft Tissue Sarcoma 57 0.817
515
KRT006 Keratoconjunctivitis 53 0.817
516
P ATR010 Atrial Heart Septal Defect 58 0.812
517
NRN004 Neuroendocrine Tumor 55 0.812
518
ENT011 Enterocolitis 55 0.806
519
P LVR013 Liver Disease 68 0.806
520
IRR002 Irritable Bowel Syndrome 65 0.806
521
FTT001 Fatty Liver Disease 61 0.806
522
PTT037 Pituitary Tumors 44 0.803
523
c BCT013 Bacterial Pneumonia 47 0.803
524
HMP001 Hemopericardium 47 0.800
525
PLC007 Placental Abruption 47 0.800
526
ADR041 Adrenal Cortical Adenoma 48 0.797
527
PLC008 Placenta Disease 49 0.797
528
c HPT003 Hepatitis a 63 0.795
529
PSD007 Pseudomyxoma Peritonei 52 0.795
530
IGG001 Iga Glomerulonephritis 50 0.794
531
ADL002 Adult Syndrome 69 0.794
532
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.794
533
c PRS130 Prostate Cancer, Hereditary, 8 32 0.794
534
c PRS136 Prostate Cancer, Hereditary, 6 33 0.794
535
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.794
536
CNT015 Central Sleep Apnea 46 0.794
537
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.794
538
PNM008 Pneumothorax 54 0.791
539
CNT016 Central Retinal Vein Occlusion 54 0.786
540
BCT004 Bacteriuria 48 0.786
541
DFC004 Deficiency Anemia 74 0.785
542
P VNT002 Ventricular Septal Defect 58 0.785
543
P ENC004 Encephalitis 61 0.778
544
c HMP029 Hemophilia a 69 0.777
545
FCT001 Factor Viii Deficiency 62 0.777
546
P EPL164 Epilepsy 70 0.775
547
ESP021 Esophageal Cancer 84 0.769
548
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.769
549
CRY005 Cryptococcosis 61 0.769
550
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.769
551
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.765
552
NRT004 Neuritis 53 0.765
553
MNT002 Mental Depression 56 0.765
554
DCT002 Ductal Carcinoma in Situ 58 0.762
555
c CRD085 Cardiomyopathy, Familial Hypertrophic, 4 51 0.759
556
BTT017 Beta-Thalassemia Major 53 0.759
557
c ATS007 Autism Spectrum Disorder 72 0.759
558
c GLC092 Glaucoma, Primary Open Angle 61 0.752
559
P MLN008 Melanoma 75 0.752
560
P HMC002 Homocystinuria 52 0.750
561
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.749
562
CRB037 Cerebral Palsy 67 0.746
563
PRN019 Perinatal Necrotizing Enterocolitis 60 0.746
564
CHN016 Cohen Syndrome 59 0.742
565
P EXN002 Exanthem 58 0.742
566
WRN001 Werner Syndrome 69 0.740
567
GYN001 Gynecomastia 48 0.740
568
INF021 Infant Gynecomastia 30 0.740
569
RSC001 Rosacea 55 0.740
570
IMM167 Immune Deficiency Disease 77 0.739
571
P ACN011 Acne 55 0.739
572
P SCL057 Scoliosis, Isolated 1 40 0.736
573
P RCT021 Rectum Cancer 54 0.736
574
P SYR003 Syringoma 36 0.732
575
P NRV007 Nervous System Disease 66 0.731
576
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.729
577
P ATS364 Autism 72 0.729
578
P END044 Endometriosis 62 0.729
579
NNS011 Nonseminomatous Germ Cell Tumor 33 0.729
580
P PNC025 Panic Disorder 52 0.725
581
P PLY011 Polycystic Ovary Syndrome 57 0.725
582
MCL006 Macular Retinal Edema 56 0.725
583
BRN071 Brain Injury 50 0.725
584
P PRC012 Pericardial Effusion 50 0.722
585
SQM006 Squamous Cell Carcinoma 59 0.718
586
RTN023 Retinitis 45 0.718
587
P BPL003 Bipolar Disorder 56 0.718
588
c HMC039 Hemochromatosis, Type 1 73 0.718
589
TRD003 Taurodontism 30 0.718
590
SCR035 Sacral Agenesis with Vertebral Anomalies 39 0.718
591
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.715
592
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.715
593
KRT001 Keratoconjunctivitis Sicca 49 0.712
594
c CNT035 Central Nervous System Disease 53 0.712
595
P RTN008 Retinitis Pigmentosa 79 0.708
596
P LNG064 Lung Cancer Susceptibility 3 70 0.708
597
P CRN035 Cranial Nerve Palsy 42 0.708
598
DNT006 Dental Pulp Necrosis 43 0.707
599
HPT022 Hepatoblastoma 54 0.707
600
CNN002 Cannabis Abuse 44 0.707
601
c MJR024 Major Affective Disorder 9 40 0.705
602
c MJR022 Major Affective Disorder 8 37 0.705
603
STT001 Status Epilepticus 58 0.705
604
DYS073 Dysphagia 53 0.701
605
P END033 Endocarditis 58 0.697
606
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.695
607
P SBR004 Seborrheic Dermatitis 44 0.695
608
OST003 Osteonecrosis 61 0.694
609
TRM010 Traumatic Brain Injury 50 0.694
610
ATR055 Atrial Septal Aneurysm 22 0.694
611
P HMN010 Hemangioma 61 0.690
612
P INT143 Interstitial Cystitis 59 0.690
613
P AVS003 Avascular Necrosis 41 0.690
614
P GRF003 Graft-Versus-Host Disease 71 0.687
615
P KDN017 Kidney Cancer 60 0.683
616
SYN005 Synostosis 43 0.683
617
PST011 Pustulosis of Palm and Sole 52 0.683
618
P PSR002 Psoriasis 63 0.683
619
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.682
620
SRC015 Sarcosinemia 38 0.682
621
P DYS007 Dyskeratosis Congenita 66 0.682
622
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.679
623
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.679
624
CHL065 Cholangiocarcinoma 58 0.679
625
INT079 Intrahepatic Cholangiocarcinoma 51 0.679
626
ADR005 Adrenal Carcinoma 61 0.679
627
P PLV020 Pelvic Organ Prolapse 58 0.676
628
LVR012 Liver Cirrhosis 62 0.676
629
P OPT009 Optic Neuritis 57 0.676
630
EST003 Eastern Equine Encephalitis 37 0.676
631
P MSC005 Muscular Dystrophy 66 0.676
632
TRC022 Tricuspid Valve Insufficiency 47 0.672
633
c CRN243 Carney Complex, Type 1 53 0.670
634
CHL122 Cholesteatoma of Middle Ear 51 0.670
635
GLN010 Glanzmann Thrombasthenia 66 0.668
636
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.668
637
THR035 Thrombasthenia 48 0.668
638
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.668
639
RSP023 Rasopathy 54 0.665
640
P UVS001 Uv-Sensitive Syndrome 40 0.665
641
P LMY004 Leiomyosarcoma 62 0.665
642
HRT012 Heart Valve Disease 53 0.665
643
STM007 Stomatitis 52 0.665
644
THY122 Thyroid Gland Cancer 59 0.662
645
P TRT010 Teratoma 50 0.661
646
SPN051 Spondylitis 51 0.657
647
INF009 Inflammatory Spondylopathy 30 0.657
648
P NNN008 Noonan Syndrome 1 76 0.653
649
PLM012 Pulmonary Sarcoidosis 53 0.653
650
INT065 Interstitial Keratitis 31 0.653
651
FSC004 Fasciitis 49 0.653
652
HMM004 Hamamy Syndrome 39 0.653
653
AND014 Androgenic Alopecia 46 0.653
654
TTN001 Tetanus Neonatorum 31 0.653
655
ADT003 Auditory System Disease 49 0.653
656
THR004 Thrombocytosis 52 0.653
657
OBS002 Obsessive-Compulsive Disorder 68 0.650
658
c SRC023 Sarcoidosis 2 44 0.648
659
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.648
660
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.648
661
P CNR004 Cone-Rod Dystrophy 2 75 0.648
662
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.648
663
PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.648
664
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.646
665
c TYP008 Type 1 Diabetes Mellitus 77 0.642
666
FTL021 Fetal Macrosomia 40 0.642
667
PLY012 Polyhydramnios 46 0.638
668
ATR017 Atrial Septal Defect Coronary Sinus 25 0.638
669
PRR015 Preauricular Fistulae, Congenital 19 0.637
670
EXC003 Excessive Tearing 32 0.637
671
BRN012 Bronchiolitis Obliterans 56 0.637
672
c ACT042 Acute Pyelonephritis 45 0.637
673
c CHR418 Chronic Leukemia 48 0.637
674
PLG002 Plague 58 0.637
675
MYC013 Mycobacterium Abscessus 42 0.637
676
SLC006 Silicosis 55 0.634
677
MDD011 Mood Disorder 62 0.634
678
c ACT134 Acute Liver Failure 57 0.634
679
CRB079 Cerebrospinal Fluid Leak 36 0.631
680
NRL005 Neurilemmoma 60 0.630
681
c PSD047 Pseudo-Turner Syndrome 52 0.630
682
P MJR001 Major Depressive Disorder 68 0.626
683
CPG001 Capgras Syndrome 26 0.626
684
P HYD006 Hydrocephalus 63 0.626
685
SXL003 Sexual Disorder 49 0.622
686
MTB004 Metabolic Acidosis 48 0.622
687
IGR001 Ige Responsiveness, Atopic 59 0.622
688
P SBS003 Substance Abuse 54 0.622
689
OLG003 Oligohydramnios 51 0.622
690
CHR100 Chronic Ulcer of Skin 57 0.618
691
PPL022 Papilloma 53 0.618
692
P ALP061 Alopecia, Androgenetic, 1 49 0.618
693
ACT119 Acute Promyelocytic Leukemia 62 0.618
694
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.618
695
BTT018 Beta-Thalassemia Intermedia 31 0.618
696
BLR013 Biliary Tract Cancer 43 0.618
697
MNT001 Mantle Cell Lymphoma 65 0.616
698
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.616
699
ACR007 Acromegaly 70 0.614
700
RYN005 Raynaud Phenomenon 45 0.614
701
EMB004 Embryonal Carcinoma 55 0.610
702
P MSC003 Muscular Atrophy 52 0.610
703
CHR103 Charge Syndrome 65 0.606
704
c PCH010 Pachyonychia Congenita 3 43 0.606
705
CHL045 Choline Deficiency Disease 39 0.606
706
INT075 Intracranial Hypertension 52 0.606
707
GNT019 Giant Cell Myocarditis 29 0.606
708
ORL015 Oral Squamous Cell Carcinoma 43 0.602
709
IMP005 Impotence 52 0.602
710
P HYP265 Hypotonia 42 0.602
711
CRH005 Crohn's Colitis 53 0.599
712
P ACT244 Acth-Independent Cushing Syndrome 37 0.598
713
c INF023 Inflammatory Breast Carcinoma 48 0.595
714
MTR001 Mature Cataract 27 0.595
715
SBC003 Subacute Bacterial Endocarditis 33 0.595
716
INS024 Insulin-Like Growth Factor I 77 0.594
717
CRD001 Cardiac Tamponade 44 0.594
718
UTR043 Uterine Sarcoma 40 0.594
719
RDC002 Radiculopathy 51 0.594
720
ETN001 Eating Disorder 59 0.594
721
P DNG005 Dengue Virus 55 0.589
722
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.589
723
VSC003 Visceral Leishmaniasis 54 0.589
724
c PRD040 Periodontitis, Chronic 52 0.585
725
CHL068 Cholestasis 61 0.585
726
MYM001 Myoma 54 0.585
727
NWC001 Newcastle Disease 48 0.585
728
P PMP001 Pemphigus 55 0.585
729
P FBR017 Fibrosarcoma 55 0.581
730
P RTN016 Retinal Degeneration 52 0.581
731
CHR072 Chordoma 57 0.577
732
CHR005 Chorioamnionitis 50 0.577
733
PRT013 Portal Hypertension 59 0.577
734
ECT026 Ectopic Pregnancy 47 0.577
735
P ICH004 Ichthyosis 56 0.577
736
P RRT020 Rare Tumor 39 0.577
737
P LKD001 Leukodystrophy 58 0.572
738
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.572
739
LMY002 Leiomyoma 51 0.572
740
P RTN018 Retinal Disease 53 0.572
741
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.572
742
CHL123 Chlamydia 58 0.572
743
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.568
744
DSS008 Disease of Mental Health 74 0.568
745
c ACT249 Acute Asthma 40 0.568
746
P BND020 Bone Disease 60 0.568
747
GTR002 Goiter 52 0.568
748
MLT001 Multiple Chemical Sensitivity 38 0.568
749
DSS032 Disease by Infectious Agent 55 0.564
750
P KRT007 Keratoconus 50 0.564
751
c SPN225 Spondyloarthropathy 1 70 0.564
752
CHL067 Cholecystitis 59 0.564
753
P PRR002 Pure Red-Cell Aplasia 46 0.564
754
PST092 Posttransplant Acute Limbic Encephalitis 29 0.564
755
P CRN038 Carney Complex Variant 63 0.559
756
P ART005 Arteriovenous Malformation 65 0.559
757
DGN001 Degenerative Disc Disease 48 0.559
758
DRY001 Dry Eye Syndrome 49 0.558
759
P OTS001 Otosclerosis 49 0.558
760
BDD001 Budd-Chiari Syndrome 62 0.555
761
WST005 West Nile Virus 55 0.555
762
P NSP012 Nasopharyngeal Carcinoma 60 0.555
763
GST045 Gastroenteritis 58 0.555
764
PLM014 Pleomorphic Adenoma 51 0.555
765
WHP002 Whiplash 35 0.555
766
P CHL066 Cholangitis 51 0.555
767
PLN007 Plantar Fasciitis 35 0.555
768
c ACT073 Acute Leukemia 59 0.550
769
KRT009 Keratosis 52 0.550
770
LPM012 Lipomatosis, Multiple 60 0.546
771
CHG001 Chagas Disease 65 0.546
772
P CLC063 Celiac Disease 1 66 0.541
773
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.541
774
KHN001 Kuhnt-Junius Degeneration 48 0.541
775
CLF001 Cleft Lip 54 0.541
776
P HYP076 Hyperthyroidism 53 0.541
777
PSR001 Psoriatic Arthritis 61 0.537
778
P MYS003 Myasthenia Gravis 68 0.532
779
P AMY004 Amyloidosis 69 0.532
780
VGN023 Vaginitis 56 0.529
781
CYN002 Cyanosis, Transient Neonatal 43 0.527
782
HYP080 Hypogonadism 49 0.527
783
P GRV001 Graves' Disease 54 0.527
784
CLN015 Colon Adenocarcinoma 64 0.527
785
P HYP077 Hypertrichosis 48 0.527
786
P TMP001 Temporal Lobe Epilepsy 49 0.527
787
ICH054 Ichthyosis, X-Linked 51 0.527
788
SPS057 Spasticity 43 0.527
789
PRP080 Peripheral Artery Disease 54 0.522
790
CHN010 Chondroma 43 0.522
791
PSY004 Psychotic Disorder 66 0.522
792
CNT060 Central Serous Chorioretinopathy 39 0.522
793
CRT015 Carotid Artery Occlusion 45 0.522
794
P ART018 Aortic Valve Insufficiency 52 0.518
795
EPC002 Epicondylitis 43 0.518
796
NRN001 Neuroendocrine Carcinoma 47 0.518
797
ADN011 Adenoid Cystic Carcinoma 68 0.513
798
P THR015 Thrombophilia 51 0.513
799
ECH003 Echinococcosis 52 0.513
800
MSC157 Muscular Dystrophy, Duchenne Type 79 0.513
801
P ORT004 Orthostatic Intolerance 62 0.513
802
PST021 Postpartum Depression 50 0.513
803
CNT056 Cantu Syndrome 48 0.508
804
NRL016 Neural Tube Defects 81 0.508
805
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.508
806
MST005 Mastitis 52 0.508
807
GNG013 Gingivitis 59 0.508
808
CHR074 Choriocarcinoma 46 0.508
809
P PLY017 Polyarteritis Nodosa 60 0.508
810
c ACT135 Acute Graft Versus Host Disease 51 0.508
811
ARG004 Argyria 26 0.508
812
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.504
813
VRC005 Varicose Veins 59 0.503
814
c ACT076 Acute Myocarditis 47 0.503
815
ART002 Arts Syndrome 66 0.503
816
GRW007 Growth Hormone Deficiency 47 0.503
817
SYN106 Syndromic Craniosynostosis 32 0.503
818
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.498
819
THY111 Thyroid Carcinoma, Familial Medullary 67 0.498
820
THY125 Thyroid Gland Medullary Carcinoma 48 0.498
821
CHR001 Churg-Strauss Syndrome 61 0.498
822
ANX004 Anoxia 40 0.498
823
P ACT010 Acth-Secreting Pituitary Adenoma 60 0.498
824
BNG077 Benign Idiopathic Neonatal Seizures 22 0.498
825
MYL005 Myelofibrosis 70 0.496
826
c ACR091 Aicardi-Goutieres Syndrome 4 35 0.496
827
SMT004 Smith-Lemli-Opitz Syndrome 69 0.496
828
c ART061 Arthrogryposis, Distal, Type 2a 58 0.496
829
PLX004 Plexopathy 29 0.496
830
BLD052 Blood Group Incompatibility 31 0.496
831
P HYP121 Hypoalphalipoproteinemia 42 0.496
832
ALT003 Alternating Exotropia 33 0.493
833
EXT022 Exotropia 42 0.493
834
CNN005 Connective Tissue Disease 66 0.488
835
HYP043 Hyperandrogenism 47 0.488
836
PRS025 Presbyopia 39 0.488
837
MCR088 Microscopic Polyangiitis 51 0.488
838
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.488
839
DSN001 De Sanctis-Cacchione Syndrome 36 0.483
840
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.483
841
LPT014 Leptin Deficiency or Dysfunction 77 0.483
842
IRN002 Iron Metabolism Disease 56 0.483
843
MLT006 Multidrug-Resistant Tuberculosis 47 0.483
844
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.478
845
P LKM062 Leukemia, Acute Lymphoblastic 69 0.478
846
HYD038 Hydrops Fetalis, Nonimmune 57 0.478
847
c LYM150 Lymphatic Malformation 7 43 0.478
848
P STR020 Strabismus 56 0.478
849
END031 Endometrial Stromal Sarcoma 45 0.478
850
MCH006 Mechanical Strabismus 40 0.478
851
MCP033 Mucopolysaccharidoses 44 0.478
852
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.473
853
APR006 Apert Syndrome 69 0.473
854
CLF027 Cleft Palate, Isolated 64 0.473
855
RBS001 Rabies 58 0.473
856
SKN006 Skin Sarcoidosis 42 0.473
857
SCH014 Schistosomiasis 56 0.473
858
P RTN022 Retinal Vein Occlusion 54 0.473
859
P DRM010 Dermatomyositis 61 0.467
860
SWN001 Swine Influenza 45 0.467
861
c CRB100 Cerebrooculofacioskeletal Syndrome 4 33 0.467
862
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.467
863
EWN003 Ewing Sarcoma 70 0.467
864
ART017 Aortic Disease 49 0.467
865
OVR094 Ovarian Epithelial Cancer 39 0.467
866
c JVN010 Juvenile Rheumatoid Arthritis 66 0.467
867
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.467
868
P MTC003 Metachromatic Leukodystrophy 71 0.462
869
CRD223 Cardiac Arrhythmia 63 0.462
870
CYS008 Cystic Echinococcosis 57 0.462
871
IRD001 Iridocyclitis 54 0.462
872
P NRF002 Neurofibromatosis 60 0.462
873
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.458
874
c OTS005 Otosclerosis 1 25 0.458
875
c FML001 Familial Atrial Fibrillation 65 0.458
876
c HYP272 Hypercholesterolemia, Familial, 3 46 0.458
877
KPR003 Keipert Syndrome 44 0.458
878
NTR005 Nutritional Deficiency Disease 60 0.458
879
P CRV039 Cervicitis 52 0.458
880
CLN045 Colonic Benign Neoplasm 48 0.458
881
MXD023 Mixed Cell Type Cancer 44 0.458
882
RTC005 Reticulosarcoma 47 0.458
883
ATX019 Ataxia with Vitamin E Deficiency 44 0.458
884
P MLG074 Malignant Mesenchymoma 40 0.458
885
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.457
886
RGH001 Right Bundle Branch Block 47 0.457
887
KRN002 Kearns-Sayre Syndrome 63 0.457
888
GRM010 Germ Cells Tumors 33 0.457
889
PRT082 Preterm Premature Rupture of the Membranes 56 0.451
890
P MNN007 Meningocele 39 0.451
891
GNG003 Gingival Recession 50 0.451
892
SYS003 Systolic Heart Failure 49 0.451
893
P SLP005 Sleep Disorder 62 0.451
894
CRB004 Cerebral Artery Occlusion 46 0.446
895
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.446
896
LNT004 Lentigines 45 0.446
897
P HML002 Hemolytic Anemia 62 0.446
898
P FCL005 Focal Segmental Glomerulosclerosis 57 0.446
899
INT066 Interstitial Lung Disease 60 0.446
900
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.446
901
P HYP083 Hypopituitarism 52 0.446
902
CLF004 Cleft Lip/palate 57 0.446
903
MCR096 Macrocephaly/autism Syndrome 44 0.440
904
PLM005 Pleomorphic Lipoma 40 0.440
905
RNL077 Renal Fibrosis 46 0.440
906
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.440
907
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.440
908
P BRS053 Breast Fibroadenoma 48 0.440
909
CRT016 Carotid Artery Disease 52 0.440
910
CLL003 Cellulitis 53 0.440
911
P URT039 Urticaria 57 0.440
912
P SYR001 Syringomyelia 47 0.440
913
P THY023 Thymoma 64 0.440
914
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.440
915
c THY107 Thymoma, Familial 42 0.440
916
P BRN022 Bronchiectasis 59 0.440
917
MYL009 Myelodysplastic Syndrome 67 0.434
918
NNL006 Non-Alcoholic Steatohepatitis 54 0.434
919
P PRK057 Parkinson Disease, Late-Onset 79 0.434
920
ACQ007 Acquired Immunodeficiency Syndrome 58 0.434
921
GNG012 Gingival Overgrowth 49 0.434
922
MYC005 Myocardial Stunning 45 0.434
923
CHR066 Chronic Fatigue Syndrome 60 0.434
924
HPR003 Heparin-Induced Thrombocytopenia 47 0.434
925
PMP014 Pemphigoid 49 0.429
926
CLB010 Coloboma of Macula 53 0.429
927
APH002 Aphasia 55 0.429
928
c CRB098 Cerebrooculofacioskeletal Syndrome 2 30 0.429
929
P PTS002 Ptosis 52 0.429
930
NNN026 Noonan Syndrome with Multiple Lentigines 65 0.429
931
MTH009 Mouth Disease 57 0.429
933
P HNT016 Huntington Disease 73 0.423
934
HPT004 Hepatic Coma 43 0.423
935
P TTR001 Tetralogy of Fallot 69 0.423
936
DYS018 Dysostosis 43 0.423
937
c SVR005 Severe Pre-Eclampsia 50 0.423
938
LYM027 Lymphopenia 56 0.423
939
P HRN001 Horner's Syndrome 45 0.423
940
RST023 Resting Heart Rate, Variation in 40 0.423
941
ALL012 Allergic Angiitis 24 0.423
942
SYS071 Systemic Autoimmune Disease 35 0.423
943
IDP091 Idiopathic Nephrotic Syndrome 49 0.423
944
P SML001 Small Cell Carcinoma 52 0.417
945
PMP006 Pemphigus Vulgaris, Familial 58 0.417
946
c ATM011 Autoimmune Hepatitis 62 0.417
947
HPT019 Hepatic Encephalopathy 59 0.417
948
GNG005 Gangliocytoma 54 0.417
949
SNG003 Single Ventricular Heart 30 0.417
950
KLD004 Keloid Disorder 39 0.417
951
CTN007 Cutaneous Leishmaniasis 61 0.417
952
c ACQ016 Acquired Pure Red Cell Aplasia 29 0.417
953
P GLM040 Glioma Susceptibility 1 70 0.411
954
DYS015 Dysentery 50 0.411
955
MLG169 Malignant Astrocytoma 57 0.411
956
ASP004 Asphyxia Neonatorum 50 0.411
957
ANR007 Anorexia Nervosa 59 0.411
958
HRP004 Herpes Zoster