Search results for ar

3316 hits were found for ar

# Family MCID Name MIFTS Score
1
AND002 Androgen Insensitivity Syndrome 63 82.798
2
P PRS040 Prostate Cancer 95 65.948
3
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 48.677
4
CMP034 Complete Androgen Insensitivity Syndrome 55 47.022
5
AND020 Androgen Insensitivity, Partial 54 44.905
6
P BRS047 Breast Cancer 97 26.363
7
P HYP284 Hypospadias 1, X-Linked 21 25.284
8
ARM004 Aromatase Excess Syndrome 52 23.991
9
END057 Endometrial Cancer 76 17.110
10
P MSC003 Muscular Atrophy 52 16.592
11
P HYP040 Hypospadias 51 16.409
12
P HPT023 Hepatocellular Carcinoma 95 15.298
13
IMM166 Immunodeficiency 27a 58 15.191
14
RNL026 Renal Tubular Acidosis with Deafness 12 15.110
15
c MYP131 Myopathy, Centronuclear, 2 51 14.483
16
P PLY011 Polycystic Ovary Syndrome 57 13.962
17
ALR002 Al-Raqad Syndrome 29 13.901
18
ALL003 Allergic Rhinitis 66 13.874
19
P OVR042 Ovarian Cancer 88 13.303
20
AZS001 Azoospermia 45 13.211
21
HYP080 Hypogonadism 49 13.202
22
c HYP788 Hypophosphatemic Rickets, Autosomal Recessive, 1 28 13.086
23
P RHN004 Rhinitis 56 13.000
24
ESP021 Esophageal Cancer 84 12.637
25
P INF032 Infertility 60 12.596
26
PRS045 Prostatic Hypertrophy 53 12.473
27
c HYP829 Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive 43 12.471
28
P HYP730 Hypogonadotropic Hypogonadism 57 12.453
29
PRS021 Prostatic Adenoma 43 12.322
30
P MLN007 Male Infertility 56 12.271
31
BRS099 Breast Ductal Carcinoma 61 11.751
32
P ALP008 Alopecia 53 11.737
33
P OST002 Osteoporosis 76 11.673
34
HYP043 Hyperandrogenism 47 11.646
35
P MTR014 Motor Neuron Disease 65 11.386
36
c CHR542 Charcot-Marie-Tooth Disease, Axonal, Type 2t 36 11.327
37
WTH001 Withdrawal Disorder 47 11.064
38
FML037 Female Breast Cancer 51 11.008
39
PRS042 Prostate Disease 42 10.976
40
c ATS494 Autosomal Recessive Distal Renal Tubular Acidosis 36 10.960
41
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 61 10.942
42
P FML018 Familial Mediterranean Fever 73 10.839
43
PLM014 Pleomorphic Adenoma 51 10.795
44
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 39 10.685
45
c CHR545 Charcot-Marie-Tooth Disease, Axonal, Type 2h 27 10.685
46
c MTC138 Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive 26 10.685
47
c CHR700 Charcot-Marie-Tooth Disease Type 2a2b 18 10.685
48
PSD009 Pseudohermaphroditism 46 10.339
49
OLG001 Oligospermia 45 10.331
50
SVR004 Severe Combined Immunodeficiency 70 10.300
51
c TYP009 Type 2 Diabetes Mellitus 91 10.251
52
GRM005 Germ Cell Cancer 46 10.182
53
END062 Endometrial Hyperplasia 47 10.160
54
P SPN046 Spinal Muscular Atrophy 62 10.095
55
PRS129 Prostatic Hyperplasia, Benign 48 10.065
56
ADN009 Adenosquamous Carcinoma 49 9.988
57
CRY035 Cryptorchidism, Unilateral or Bilateral 57 9.786
58
AND014 Androgenic Alopecia 46 9.728
59
P MYP004 Myopathy 67 9.610
60
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 9.584
61
P AXN002 Axenfeld-Rieger Syndrome 62 9.537
62
P TRN020 Turner Syndrome 67 9.536
63
GYN001 Gynecomastia 48 9.389
64
P SKN015 Skin Carcinoma 71 9.223
65
TST014 Testicular Cancer 51 9.137
66
P EST001 Estrogen-Receptor Positive Breast Cancer 49 9.111
67
P ATS364 Autism 72 9.065
68
PRM013 Premature Menopause 57 8.981
69
LYM157 Lymph Node Carcinoma 33 8.920
70
DCT002 Ductal Carcinoma in Situ 58 8.882
71
NRM005 Neuromuscular Disease 62 8.774
72
TRN007 Transsexualism 38 8.762
73
P PRD006 Prader-Willi Syndrome 60 8.742
74
EST002 Estrogen-Receptor Negative Breast Cancer 45 8.739
75
P BRS053 Breast Fibroadenoma 48 8.713
76
P ACN011 Acne 55 8.709
77
c ATS007 Autism Spectrum Disorder 71 8.620
78
c ATS452 Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy 18 8.595
79
SPN369 Spinal Disease 43 8.437
80
P ART018 Aortic Valve Insufficiency 52 8.423
81
MMM001 Mammary Paget's Disease 53 8.412
82
c WLM013 Wilms Tumor 1 65 8.396
83
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 8.369
84
P SML001 Small Cell Carcinoma 52 8.364
85
ING001 Inguinal Hernia 59 8.346
86
SBC011 Sebaceous Adenocarcinoma 43 8.334
87
P MCH002 Machado-Joseph Disease 62 8.316
88
P OVR049 Ovarian Disease 50 8.316
89
P TST026 Testicular Germ Cell Cancer 42 8.316
90
VRC001 Varicocele 48 8.289
91
BRR014 Barrett Esophagus 66 8.282
92
PGT003 Paget Disease, Extramammary 48 8.268
93
PRS006 Prostatic Acinar Adenocarcinoma 28 8.260
94
GND002 Gender Identity Disorder 40 8.237
95
PRM003 Premature Ejaculation 44 8.173
96
P ANG001 Angelman Syndrome 64 8.151
97
PLM018 Pulmonary Sclerosing Hemangioma 36 8.113
98
OLG022 Oligoasthenoteratozoospermia 36 8.082
99
HRM002 Hermaphroditism 35 8.082
100
c PST093 Posterior Hypospadias 19 8.063
101
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 8.013
102
P ASP001 Asperger Syndrome 48 8.013
103
SRT002 Sertoli Cell Tumor 38 8.013
104
c SPN294 Spinocerebellar Ataxia 1 53 7.944
105
SWT002 Sweat Gland Cancer 41 7.944
106
P ALP061 Alopecia, Androgenetic, 1 48 7.936
107
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 7.871
108
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 7.839
109
c CHR650 Charcot-Marie-Tooth Disease, Axonal, Type 2b1 46 7.653
110
HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 35 7.653
111
c ATS438 Autosomal Recessive Spastic Ataxia 24 7.653
112
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 54 7.624
113
RNL120 Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation 28 7.555
114
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 7.555
115
c SPS159 Spastic Paraplegia 9b, Autosomal Recessive 40 7.555
116
c CHR656 Charcot-Marie-Tooth Disease, Demyelinating, Type 1f 49 7.555
117
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 28 7.555
118
HRD175 Hereditary Motor and Sensory Neuropathy with Acrodystrophy 8 7.555
119
DCK002 Dock8 Immunodeficiency Syndrome 26 7.555
120
SPP011 Suppression of Tumorigenicity 12 61 7.472
122
TFR002 Tafro Syndrome 34 7.171
123
PNS014 Penis Agenesis 38 7.140
124
DBT007 Diabetic Cataract 36 7.027
125
APC004 Apocrine Adenocarcinoma 37 6.629
126
P RTN008 Retinitis Pigmentosa 79 6.415
127
c 46X082 46,xy Sex Reversal 52 6.362
128
P TST021 Testicular Germ Cell Tumor 61 6.344
129
P EYD002 Eye Disease 57 6.294
130
P DSR090 Disorder of Sexual Development 45 6.268
131
SXL003 Sexual Disorder 49 6.206
132
INT323 Intraocular Pressure Quantitative Trait Locus 63 6.182
133
DSS008 Disease of Mental Health 74 6.119
134
PLM009 Pleomorphic Adenoma Carcinoma 33 6.075
135
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 6.075
136
TST015 Testicular Disease 42 6.031
137
c SPR089 Spermatogenic Failure 4 32 6.007
138
VGN023 Vaginitis 56 5.800
139
OCL006 Ocular Hypertension 53 5.790
140
PRS007 Prostate Calculus 25 5.755
141
c EPL091 Epilepsy, Idiopathic Generalized 3 29 5.737
142
XLN228 X-Linked Recessive Disease 24 5.737
143
P AML002 Amelogenesis Imperfecta 56 5.715
144
LVR032 Liver Adenomatosis 28 5.715
145
c PCH010 Pachyonychia Congenita 3 43 5.712
146
c HYP595 Hypertension, Essential 84 5.619
147
c EPL089 Epilepsy, Idiopathic Generalized 4 14 5.618
148
MLR005 Male Reproductive Organ Benign Neoplasm 21 5.618
149
XLN230 X-Linked Monogenic Disease 20 5.618
150
c EPL092 Epilepsy, Idiopathic Generalized 2 22 5.618
151
c MCR228 Microphthalmia, Syndromic 13 30 5.618
152
c AML044 Amelogenesis Imperfecta, Type Ig 54 5.618
153
CMP087 Complement Component 7 Deficiency 37 5.618
154
c SPR042 Spermatogenic Failure 8 32 5.618
155
c EPL090 Epilepsy, Idiopathic Generalized 5 18 5.618
156
TTH005 Teeth Hard Tissue Disease 27 5.618
157
c 46X030 46,xy Sex Reversal 9 43 5.618
158
CST005 Castleman Disease 56 5.618
159
MLR007 Male Reproductive System Disease 32 5.618
160
WLF006 Wolffian Duct Adenocarcinoma 33 5.618
161
OVR016 Ovarian Endometrioid Stromal Sarcoma 25 5.618
162
ONC001 Oncocytic Breast Carcinoma 27 5.618
163
SWT003 Sweat Gland Disease 35 5.618
164
PRS022 Prostate Leiomyoma 22 5.618
165
PRS017 Prostate Neuroendocrine Neoplasm 26 5.618
166
PRS019 Prostate Adenoid Cystic Carcinoma 23 5.618
167
MLR006 Male Reproductive Organ Cancer 40 5.618
168
PRS027 Prostate Transitional Cell Carcinoma 25 5.618
169
P HRD018 Hair Disease 43 5.618
170
NDL006 Nodular Prostate 24 5.618
171
c BRN145 Bronchiectasis 3 26 5.618
172
VLV016 Vulvar Apocrine Adenocarcinoma 25 5.618
173
APC005 Apocrine Sweat Gland Neoplasm 31 5.618
174
SBC017 Sebaceous Gland Disease 42 5.618
175
ACT228 Acute Radiation Syndrome 30 5.234
176
P BLD134 Bladder Cancer 79 4.838
177
P OPN001 Open-Angle Glaucoma 55 4.823
178
PRT037 Pertussis 49 4.456
179
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.412
180
P CTR002 Cataract 59 4.363
181
P GST053 Gastric Cancer 82 4.156
182
P LNG032 Lung Cancer 98 4.043
183
OCL010 Ocular Hypotension 37 4.040
184
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.029
185
PRS047 Prostatitis 57 4.012
186
GST103 Gastric Cancer, Hereditary Diffuse 68 4.004
187
P AST005 Asthma 75 3.961
188
BLD173 Bladder Small Cell Carcinoma 44 3.687
189
MNN043 Meningioma, Familial 79 3.626
190
AGN016 Aging 53 3.569
191
CYT002 Cytokine Deficiency 43 3.513
193
P GLM040 Glioma Susceptibility 1 70 3.397
194
P LNG064 Lung Cancer Susceptibility 3 69 3.366
195
ALL029 Allergic Disease 61 3.314
196
CLN015 Colon Adenocarcinoma 64 3.290
197
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.180
198
GST040 Gastric Adenocarcinoma 66 3.168
199
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.133
200
c DLT002 Dilated Cardiomyopathy 79 3.006
201
P PNC035 Pancreatic Cancer 87 2.966
202
P MYL006 Myeloid Leukemia 60 2.950
203
HYP266 Hypoxia 56 2.947
204
c LKM061 Leukemia, Acute Myeloid 83 2.923
205
P ANR048 Aniridia 1 66 2.891
206
SML009 Small Intestine Adenocarcinoma 57 2.886
207
c PRS097 Prostate Cancer, Hereditary, 1 38 2.884
208
KHN001 Kuhnt-Junius Degeneration 48 2.866
209
P RHM011 Rheumatoid Arthritis 81 2.831
210
c PRS114 Prostate Cancer, Hereditary, 2 33 2.809
211
c PRS130 Prostate Cancer, Hereditary, 8 32 2.806
212
c PRS136 Prostate Cancer, Hereditary, 6 33 2.806
213
P LKM002 Leukemia 65 2.800
214
P ART022 Arthritis 70 2.787
215
P PRK039 Parkinsonism 55 2.785
216
GLB002 Glioblastoma 67 2.703
217
P LYM118 Lymphoma 66 2.690
218
ADN011 Adenoid Cystic Carcinoma 68 2.680
219
P PNM007 Pneumonia 64 2.672
220
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.660
221
c PRS070 Prostate Cancer, Hereditary, 12 22 2.655
222
c PRS071 Prostate Cancer, Hereditary, 13 25 2.655
223
c PRS117 Prostate Cancer, Hereditary, 11 24 2.655
224
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 2.655
225
P TRM003 Tremor 50 2.612
226
ISC004 Ischemia 61 2.597
227
P TMR010 Tumor Predisposition Syndrome 69 2.586
228
GLM045 Glioma 62 2.579
229
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 2.574
230
c CLR087 Colorectal Cancer 12 34 2.574
231
MYL069 Myeloma, Multiple 76 2.565
232
P DRM053 Dermatitis, Atopic 65 2.530
233
LNG099 Lung Disease 62 2.512
234
SPN035 Spindle Cell Sarcoma 51 2.502
235
SRC014 Sarcoma 64 2.502
236
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.494
237
ADL002 Adult Syndrome 69 2.489
238
LNG039 Lung Squamous Cell Carcinoma 57 2.479
239
SQM006 Squamous Cell Carcinoma 59 2.463
240
P KDN017 Kidney Cancer 60 2.461
241
HLX001 Helix Syndrome 47 2.458
242
P BCL017 B-Cell Lymphoma 57 2.455
243
48X005 48,xyyy 39 2.420
244
AMD002 Amed Syndrome, Digenic 36 2.405
245
c ATR087 Atrial Standstill 1 74 2.400
246
LYM002 Lymphoplasmacyte-Rich Meningioma 35 2.382
247
SCR001 Secretory Meningioma 40 2.382
248
INT395 Intracranial Meningioma 47 2.382
249
INT066 Interstitial Lung Disease 60 2.347
250
P LKM062 Leukemia, Acute Lymphoblastic 69 2.344
251
CYS001 Cystic Fibrosis 77 2.332
252
ADN089 Adenosquamous Lung Carcinoma 51 2.329
253
LPP008 Lipoprotein Quantitative Trait Locus 65 2.319
254
47X002 47,xyy 47 2.306
255
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 2.278
256
HYP066 Hyperglycemia 60 2.242
257
P ADN016 Adenocarcinoma 63 2.242
258
ART016 Aortic Aneurysm 68 2.199
259
P HRT032 Heart Disease 84 2.194
260
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.161
261
DRM006 Dermatitis 61 2.158
262
P RTN024 Retinoblastoma 72 2.153
263
HRT011 Heart Septal Defect 49 2.134
264
P CHR012 Chronic Granulomatous Disease 69 2.132
265
P SLP006 Sleep Apnea 69 2.128
266
OST159 Osteogenic Sarcoma 66 2.116
267
ATR003 Atrophic Rhinitis 40 2.112
268
c MCR115 Microvascular Complications of Diabetes 5 65 2.110
269
P VNT002 Ventricular Septal Defect 58 2.108
270
P EXN002 Exanthem 58 2.074
271
c MJR022 Major Affective Disorder 8 37 2.072
272
c MJR024 Major Affective Disorder 9 40 2.072
273
P BPL003 Bipolar Disorder 56 2.072
274
ANG054 Angina Pectoris 65 2.053
275
ANR040 Aneurysm 60 2.047
276
P MYC007 Myocardial Infarction 69 2.039
277
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 2.039
278
LYM133 Lymphoma, Hodgkin, Classic 69 2.021
279
MNT001 Mantle Cell Lymphoma 65 2.014
280
P DRM010 Dermatomyositis 61 2.002
281
P DBT009 Diabetes Mellitus 67 1.996
282
MTR002 Mitral Valve Insufficiency 51 1.994
283
ANT039 Antisynthetase Syndrome 55 1.994
284
STR067 Stroke, Ischemic 79 1.991
286
RFR003 Refractive Error 41 1.985
287
HMN044 Human Immunodeficiency Virus Type 1 76 1.972
288
P MYS005 Myositis 55 1.971
289
P NTR004 Neutropenia 62 1.948
290
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.943
291
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.943
292
ALC007 Alcohol Dependence 65 1.943
293
P RCT021 Rectum Cancer 54 1.932
294
MCL006 Macular Retinal Edema 56 1.922
295
IGR001 Ige Responsiveness, Atopic 58 1.915
296
P OLG002 Oligodendroglioma 66 1.908
297
ANX010 Anxiety 70 1.884
298
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 1.880
299
CNG034 Congestive Heart Failure 69 1.868
300
P PLY041 Polymyositis 58 1.858
301
P NRF002 Neurofibromatosis 60 1.853
302
RHB024 Rhabdomyosarcoma 2 65 1.850
303
NRR001 Neuroretinitis 42 1.845
304
RTN023 Retinitis 45 1.845
305
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.822
306
INS024 Insulin-Like Growth Factor I 77 1.822
307
GST092 Gastroesophageal Reflux 59 1.821
308
DWN001 Down Syndrome 70 1.820
309
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.805
310
P DST107 Distal Renal Tubular Acidosis 48 1.800
311
INT007 Intermediate Coronary Syndrome 53 1.798
312
MLD006 Mal De Meleda 45 1.788
313
P END033 Endocarditis 58 1.785
314
ATH013 Atherosclerosis Susceptibility 63 1.769
315
BRK010 Burkitt Lymphoma 65 1.764
316
P CNJ013 Conjunctivitis 66 1.761
317
P MYP006 Myopia 55 1.753
318
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.740
319
P HPT021 Hepatitis 68 1.732
320
MCL027 Macular Dystrophy, Dominant Cystoid 51 1.716
321
PST028 Post-Traumatic Stress Disorder 58 1.714
322
CHL014 Cholera 62 1.712
323
BCT022 Bacterial Infectious Disease 55 1.704
324
P HNT016 Huntington Disease 73 1.703
325
CHL147 Chlamydia Pneumonia 47 1.698
326
c BSL007 Basal Cell Carcinoma 67 1.689
327
P CHR345 Chronic Pain 50 1.687
328
LWC001 Low Compliance Bladder 44 1.687
329
ART074 Aortic Dissection 53 1.683
330
MYL009 Myelodysplastic Syndrome 67 1.677
331
P SLV026 Salivary Gland Carcinoma 59 1.676
332
BRN002 Bronchiolitis 57 1.671
333
c SML038 Small Cell Cancer of the Lung 68 1.667
334
P RSP003 Respiratory Failure 73 1.659
335
P SRC025 Sarcoidosis 1 70 1.655
336
IMM167 Immune Deficiency Disease 76 1.653
337
P LKM071 Leukemia, Chronic Lymphocytic 74 1.648
338
HYP458 Hyper Ige Syndrome 60 1.643
339
IMM180 Immunodeficiency 28 39 1.642
340
CLT003 Colitis 63 1.633
341
AST006 Astigmatism 46 1.607
342
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.605
343
NRF007 Neurofibroma 63 1.597
344
ALL006 Allergic Asthma 55 1.597
345
RYN005 Raynaud Phenomenon 45 1.595
346
P END044 Endometriosis 62 1.594
347
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.592
348
DPR016 Depression 64 1.578
349
P VSC007 Vascular Disease 62 1.557
350
BRN012 Bronchiolitis Obliterans 56 1.550
351
P CHR071 Charcot-Marie-Tooth Disease 64 1.549
352
P MSC005 Muscular Dystrophy 66 1.549
353
SFT003 Soft Tissue Sarcoma 43 1.547
354
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.532
355
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.532
356
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.532
357
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.532
358
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.532
359
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.532
360
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.532
361
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.532
362
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.532
363
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.523
364
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.520
365
P NRB001 Neuroblastoma 66 1.514
366
EXF001 Exfoliation Syndrome 55 1.508
367
c GLC092 Glaucoma, Primary Open Angle 60 1.506
368
c PRM038 Primary Agammaglobulinemia 47 1.492
369
DBT006 Diabetic Macular Edema 48 1.489
370
P MLN008 Melanoma 75 1.485
371
c CHR684 Chronic Kidney Disease 73 1.481
372
P FLL037 Follicular Lymphoma 66 1.477
373
TTH006 Tooth Disease 51 1.472
374
P NSP012 Nasopharyngeal Carcinoma 60 1.469
375
IMM186 Immunodeficiency 27b 47 1.450
376
P DMN002 Dementia 65 1.448
377
c ART115 Aortic Valve Disease 1 72 1.446
378
PRP016 Paraplegia 52 1.442
379
INF021 Infant Gynecomastia 30 1.440
380
GLL048 Glial Tumor 51 1.440
381
P HYP098 Hypereosinophilic Syndrome 66 1.439
382
P BRC003 Brachyolmia 36 1.438
383
c MCR133 Microvascular Complications of Diabetes 4 41 1.437
384
c MCR113 Microvascular Complications of Diabetes 3 52 1.437
385
c MCR130 Microvascular Complications of Diabetes 6 41 1.437
386
c MCR120 Microvascular Complications of Diabetes 7 47 1.437
387
P DRR001 Diarrhea 55 1.436
388
c HYP836 Hypercholesterolemia, Familial, 1 73 1.432
389
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.413
390
P PLM037 Pulmonary Hypertension 69 1.405
391
ART002 Arts Syndrome 66 1.402
392
c HPT016 Hepatitis B 62 1.396
393
CNS004 Constipation 56 1.392
394
END041 Endometrial Adenocarcinoma 63 1.386
395
c THR092 Thrombophilia Due to Thrombin Defect 74 1.381
396
LYM019 Lymphosarcoma 46 1.379
397
OTT002 Otitis Media 70 1.377
398
END086 End Stage Renal Disease 54 1.376
399
SBC016 Subacute Delirium 42 1.367
400
ACT084 Acute Stress Disorder 53 1.361
401
P LVR013 Liver Disease 68 1.357
402
CRB004 Cerebral Artery Occlusion 45 1.357
403
P SZR006 Seizure Disorder 69 1.356
404
MLG169 Malignant Astrocytoma 57 1.353
405
OVR094 Ovarian Epithelial Cancer 39 1.345
406
ART140 Arteries, Anomalies of 52 1.332
407
LPD008 Lipid Metabolism Disorder 61 1.332
408
P THR014 Thrombocytopenia 66 1.329
409
SKN019 Skin Melanoma 70 1.329
410
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 52 1.326
411
ASP030 Aspirin Resistance 41 1.326
412
P BRS044 Breast Adenocarcinoma 58 1.322
413
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.308
414
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.307
415
CRD132 Cardiac Conduction Defect 59 1.304
416
AMN001 Amenorrhea 53 1.304
417
ORL015 Oral Squamous Cell Carcinoma 43 1.298
418
ART012 Aortitis 41 1.293
419
c HRD010 Hereditary Spastic Paraplegia 65 1.286
420
IRR002 Irritable Bowel Syndrome 64 1.284
421
CHR463 Chronic Actinic Dermatitis 37 1.269
422
MLR004 Malaria 77 1.267
423
P OVR082 Overgrowth Syndrome 41 1.267
424
P CRN300 Coronary Heart Disease 1 73 1.263
425
ORL011 Oral Cancer 60 1.251
426
P LYM033 Lymphoproliferative Syndrome 59 1.251
427
NRL005 Neurilemmoma 60 1.251
428
PLM029 Palmoplantar Keratosis 48 1.250
429
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.245
430
SKN022 Skin Squamous Cell Carcinoma 53 1.245
431
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.245
432
PLS009 Plasma Cell Neoplasm 64 1.244
433
IMM178 Immunodeficiency 31b 40 1.243
434
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.240
435
SYN036 Syncope 44 1.239
436
P DNG005 Dengue Virus 55 1.238
437
P BND020 Bone Disease 60 1.235
438
P PLM036 Pulmonary Fibrosis 65 1.234
439
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.231
440
ACT003 Acute Kidney Tubular Necrosis 46 1.231
441
ANX004 Anoxia 40 1.231
442
P ATR011 Atrial Fibrillation 66 1.228
443
CLR030 Clear Cell Renal Cell Carcinoma 53 1.223
444
P CRD119 Cardiac Arrest 68 1.221
445
P ALC033 Alcohol Use Disorder 67 1.219
446
CHR100 Chronic Ulcer of Skin 57 1.217
447
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 51 1.204
448
c SPS025 Spastic Paraplegia 15 30 1.204
449
ACS001 Acoustic Neuroma 55 1.203
450
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.202
451
c PRG020 Paragangliomas 3 39 1.198
452
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 1.192
453
BNR002 Bone Resorption Disease 47 1.190
454
MYC006 Mycosis Fungoides 64 1.188
455
P SCL018 Scoliosis 57 1.186
456
DYS073 Dysphagia 53 1.180
457
RST023 Resting Heart Rate, Variation in 40 1.176
458
OST012 Osteoarthritis 77 1.175
459
P HMN010 Hemangioma 61 1.173
460
P PRS038 Personality Disorder 65 1.170
461
PLL012 Pollen Allergy 44 1.170
462
PLM010 Pulmonary Edema 54 1.170
463
PRT112 Portal Hypertension, Noncirrhotic 29 1.168
464
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.166
465
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.166
466
MRF001 Marfan Syndrome 76 1.166
467
P URN019 Urinary Tract Infection 48 1.166
468
P RTN022 Retinal Vein Occlusion 54 1.166
469
c MSM022 Mismatch Repair Cancer Syndrome 1 69 1.164
470
c GLM043 Glioma Susceptibility 9 30 1.164
471
c GLM025 Glioma Susceptibility 2 30 1.164
472
c GLM047 Glioma Susceptibility 3 32 1.164
473
c ART101 Aortic Valve Disease 2 65 1.164
474
RCK004 Rickets 64 1.163
475
CHR048 Chronic Rhinitis 46 1.153
476
P ADL017 Adult T-Cell Leukemia 53 1.146
477
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.146
478
c LKM005 Leukemia, T-Cell, Chronic 33 1.146
479
c ACT075 Acute Myocardial Infarction 55 1.135
480
HMP009 Haemophilus Influenzae 41 1.128
481
CHL123 Chlamydia 58 1.125
482
P INS002 in Situ Carcinoma 52 1.124
483
LYM040 Lymphoblastic Lymphoma 53 1.124
484
GNR004 Generalized Anxiety Disorder 54 1.121
485
P CTN015 Cutaneous T Cell Lymphoma 48 1.118
486
PLY150 Polykaryocytosis Inducer 29 1.117
487
P EPL164 Epilepsy 70 1.117
488
SPN186 Spinal Cord Injury 60 1.117
489
P KDN018 Kidney Disease 71 1.113
490
c HPT073 Hepatitis C Virus 70 1.108
491
P ALZ034 Alzheimer Disease 87 1.103
492
NNL006 Non-Alcoholic Steatohepatitis 54 1.103
493
TLN003 Telangiectasis 51 1.103
494
P MYC084 Mycobacterium Tuberculosis 1 68 1.099
495
c MSC171 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 41 1.092
496
P ENC004 Encephalitis 61 1.092
497
LMY002 Leiomyoma 51 1.092
498
SKN016 Skin Disease 63 1.092
499
P BRN022 Bronchiectasis 59 1.092
500
P DYS154 Dystonia 64 1.088
501
MSL001 Measles 61 1.088
502
PRP036 Peripheral T-Cell Lymphoma 52 1.086
503
P LMY004 Leiomyosarcoma 62 1.081
504
CVD001 Covid-19 59 1.075
505
PRT036 Peritonitis 65 1.074
506
P ADL010 Adult Respiratory Distress Syndrome 70 1.073
507
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.070
508
c MGR028 Migraine with or Without Aura 1 63 1.065
509
APN008 Apnea, Obstructive Sleep 66 1.065
510
P CRD246 Cardiovascular System Disease 55 1.063
511
ANG046 Angioimmunoblastic T-Cell Lymphoma 50 1.062
512
MSC157 Muscular Dystrophy, Duchenne Type 78 1.058
513
c LKM060 Leukemia, Acute Lymphoblastic 3 49 1.055
514
P MLG074 Malignant Mesenchymoma 40 1.055
515
c CHR064 Chronic Monocytic Leukemia 35 1.055
516
AND005 Androgen Insensitivity Syndrome, Mild 21 1.055
517
P MTR003 Mitral Valve Stenosis 53 1.054
518
P MLT020 Multiple Sclerosis 79 1.053
519
FTT001 Fatty Liver Disease 61 1.052
520
ATM095 Autoimmune Disease 61 1.049
521
VSM001 Vasomotor Rhinitis 38 1.049
522
NRM004 Neuroma 49 1.048
523
P GND004 Gonadal Dysgenesis 46 1.045
524
P PSR002 Psoriasis 63 1.041
525
MSC007 Muscle Hypertrophy 64 1.038
526
EPT021 Epithelial Recurrent Erosion Dystrophy 45 1.038
527
P LPS004 Lupus Erythematosus 61 1.037
528
MLD018 Mild Cognitive Impairment 48 1.035
529
PLS025 Plasmablastic Lymphoma 47 1.034
530
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.034
531
LYM027 Lymphopenia 56 1.032
532
P RTN016 Retinal Degeneration 52 1.032
533
P SPN081 Spondylocostal Dysostosis, Autosomal Recessive 47 1.029
534
PST011 Pustulosis of Palm and Sole 52 1.028
535
BCK006 Back Pain 43 1.028
536
RTN017 Retinal Detachment 60 1.025
537
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 1.025
538
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.024
539
ACT098 Acute Erythroid Leukemia 55 1.022
540
P GRV001 Graves' Disease 54 1.022
541
KRT002 Keratomalacia 54 1.022
542
GLS001 Gliosarcoma 63 1.017
543
c SPN225 Spondyloarthropathy 1 70 1.017
544
SPN051 Spondylitis 51 1.017
545
INF009 Inflammatory Spondylopathy 30 1.017
546
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 1.015
547
PSD021 Pseudovaginal Perineoscrotal Hypospadias 44 1.009
548
DNT012 Dental Caries 53 1.007
549
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 67 1.002
550
RTC005 Reticulosarcoma 47 0.999
551
FDL002 Food Allergy 47 0.999
552
P URT039 Urticaria 57 0.999
553
TXC005 Toxic Shock Syndrome 61 0.998
554
ALL009 Allergic Conjunctivitis 51 0.996
555
TLR001 Tularemia 56 0.995
556
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 41 0.995
557
OCL069 Ocular Motor Apraxia 57 0.994
558
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.994
559
DBT010 Diabetic Neuropathy 54 0.992
560
P ANP001 Anaplastic Large Cell Lymphoma 59 0.989
561
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.989
562
c MSC177 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 42 0.988
563
THR024 Thrombosis 56 0.988
564
P PNC044 Pancreatitis 61 0.988
565
c SCL052 Scleroderma, Familial Progressive 60 0.985
566
c ACT027 Acute Pancreatitis 60 0.981
567
RTN020 Retinal Vascular Disease 45 0.980
568
FCT007 Factor Vii Deficiency 64 0.977
569
CRB037 Cerebral Palsy 66 0.976
570
P PLY019 Polyneuropathy 52 0.976
571
P HDC001 Headache 56 0.976
572
c LKM063 Leukemia, Chronic Myeloid 70 0.974
573
P CNR004 Cone-Rod Dystrophy 2 74 0.971
574
HRT012 Heart Valve Disease 53 0.970
575
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.967
576
c MJR006 Major Affective Disorder 5 32 0.967
577
c MJR003 Major Affective Disorder 6 32 0.967
578
OBS002 Obsessive-Compulsive Disorder 67 0.966
579
SPS019 Spastic Paraparesis 38 0.966
580
ACT119 Acute Promyelocytic Leukemia 62 0.962
581
P RBL001 Rubella 58 0.962
582
ART015 Aortic Valve Prolapse 24 0.960
583
PLM033 Pulmonary Embolism 58 0.959
584
ACQ007 Acquired Immunodeficiency Syndrome 58 0.957
585
LMY014 Leiomyoma, Uterine 55 0.957
586
c GRV008 Graves Disease 1 54 0.957
587
P MTC003 Metachromatic Leukodystrophy 71 0.952
588
PLM001 Pulmonary Tuberculosis 69 0.952
589
c MSC173 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 46 0.951
590
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.948
591
P LKD001 Leukodystrophy 58 0.947
592
P CNT004 Centronuclear Myopathy 56 0.946
593
P PRM011 Primary Ciliary Dyskinesia 68 0.946
594
PPL004 Papillary Squamous Carcinoma 39 0.944
595
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.942
596
P HRP006 Herpes Simplex 65 0.942
597
INF034 Infective Endocarditis 53 0.940
598
INF027 Infiltrative Basal Cell Carcinoma 34 0.940
599
HYP006 Hypertensive Heart Disease 48 0.932
600
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.932
601
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 0.926
602
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.926
603
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.923
604
CHL065 Cholangiocarcinoma 57 0.922
605
INT079 Intrahepatic Cholangiocarcinoma 51 0.922
606
P PRN023 Prion Disease 60 0.917
607
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.917
608
CRV035 Cervical Cancer 72 0.917
609
P GST044 Gastritis 55 0.917
610
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 60 0.912
611
HYP005 Hypokalemia 55 0.912
612
PST092 Posttransplant Acute Limbic Encephalitis 29 0.912
613
c MSC176 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 48 0.908
614
c SPN310 Spondylocostal Dysostosis 1, Autosomal Recessive 46 0.908
615
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.908
616
KRT009 Keratosis 52 0.907
617
RSP021 Respiratory Allergy 41 0.907
618
P MMP001 Mumps 56 0.901
619
END011 Endometriosis of Ovary 40 0.899
620
P ART021 Arteriosclerosis 53 0.896
621
P NRP001 Neuropathy 59 0.891
622
LBL001 Lobular Neoplasia 54 0.890
623
ENT011 Enterocolitis 55 0.890
625
FBR047 Fibromyalgia 57 0.881
626
CRB039 Cerebrovascular Disease 65 0.881
627
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.880
628
MNN042 Meningioma, Radiation-Induced 51 0.880
629
P PLN008 Peeling Skin Syndrome 43 0.880
630
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 0.880
631
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.880
632
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.880
633
FLL041 Follicular Lymphoma 1 44 0.880
634
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.880
635
c NRF023 Neurofibromatosis, Type Ii 70 0.880
636
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.880
637
c BLD140 Blood Group, I System 47 0.880
638
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.880
639
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.880
640
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 0.880
641
WLD007 Waldenstroem's Macroglobulinemia 59 0.880
642
PRL017 Prolymphocytic Leukemia 47 0.880
643
LYM012 Lymphoplasmacytic Lymphoma 50 0.880
644
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 0.880
645
NSL029 Nasal Type Extranodal Nk/t-Cell Lymphoma 41 0.880
646
FBR002 Fibrosarcoma of Bone 47 0.880
647
FNG017 Fungal Infectious Disease 54 0.880
648
SPN021 Spinal Meningioma 43 0.880
649
INT054 Intraocular Lymphoma 48 0.880
650
HDG004 Hodgkin's Granuloma 22 0.880
651
MCR004 Macroglobulinemia 48 0.880
652
IND017 Indolent Plasma Cell Myeloma 41 0.880
653
SZR001 Sezary's Disease 60 0.880
654
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.880
655
HDG006 Hodgkin's Paragranuloma 22 0.880
656
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 0.880
657
LYM051 Lymphomatoid Granulomatosis 44 0.880
658
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.880
659
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.879
661
ANG020 Angiosarcoma 63 0.878
662
TRC022 Tricuspid Valve Insufficiency 46 0.877
663
CLF001 Cleft Lip 54 0.876
664
ARG003 Argyll Robertson Pupil 24 0.872
665
P CLR023 Colorectal Cancer 100 0.869
666
P TCD001 Tic Disorder 50 0.868
667
ECH003 Echinococcosis 52 0.868
668
P SLP005 Sleep Disorder 61 0.866
669
RNL077 Renal Fibrosis 46 0.862
670
P TMP001 Temporal Lobe Epilepsy 49 0.862
671
IMP005 Impotence 52 0.861
672
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.858
673
9Q2001 9q22.3 Microdeletion 24 0.858
674
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.856
675
PNC001 Pancytopenia 52 0.856
676
P AXN001 Axonal Neuropathy 33 0.856
677
P HYP265 Hypotonia 42 0.850
678
HYP060 Hyperinsulinism 53 0.850
679
P MJR007 Major Affective Disorder 1 42 0.848
680
c MJR008 Major Affective Disorder 2 34 0.848
681
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.848
682
c MJR023 Major Affective Disorder 7 33 0.848
683
c MJR004 Major Affective Disorder 4 28 0.848
684
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.844
685
HRW001 Hair Whorl 35 0.838
686
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.833
687
P CRC039 Coarctation of Aorta 46 0.831
688
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.831
689
c SPR086 Spermatogenic Failure 3 47 0.831
690
P PTS002 Ptosis 52 0.825
691
PRT013 Portal Hypertension 59 0.825
692
CRC021 Carcinosarcoma 62 0.824
693
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.818
694
MLT135 Multiple Sulfatase Deficiency 53 0.818
695
CLL003 Cellulitis 53 0.818
696
JPN002 Japanese Encephalitis 61 0.818
697
FLL027 Fallopian Tube Carcinoma 66 0.817
698
CYC001 Cycloplegia 35 0.811
699
CRT013 Carotid Stenosis 51 0.811
700
PLC008 Placenta Disease 48 0.811
701
P PRD008 Periodontitis 63 0.810
702
P HYP086 Hypothyroidism 68 0.807
703
THY029 Thyroid Carcinoma 55 0.807
704
P CND005 Cone Dystrophy 47 0.805
705
CNT047 Contact Dermatitis 56 0.805
706
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.805
707
P BNG002 Benign Meningioma 36 0.805
708
P GLL022 Guillain-Barre Syndrome 59 0.805
709
ADN067 Adenoid Hypertrophy 38 0.804
710
c VRL010 Viral Hepatitis 52 0.798
711
c HPT003 Hepatitis a 63 0.795
712
P PRP019 Peripheral Nervous System Disease 57 0.792
713
P STR020 Strabismus 56 0.790
714
P KLZ004 Kala-Azar 1 41 0.790
715
LSH001 Leishmaniasis 63 0.790
716
MCH006 Mechanical Strabismus 40 0.790
717
BST008 Bestrophinopathy, Autosomal Recessive 47 0.788
718
NWC001 Newcastle Disease 47 0.788
719
c LMB073 Limb-Girdle Muscular Dystrophy Type 1a 34 0.788
720
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.787
721
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.787
722
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.783
723
P BRC006 Brachydactyly 52 0.783
724
c SPR009 Sporadic Breast Cancer 42 0.783
725
GRM010 Germ Cells Tumors 33 0.783
726
LVR012 Liver Cirrhosis 62 0.783
727
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.780
728
P LTR001 Lateral Sclerosis 57 0.780
729
CRH001 Crohn's Disease 80 0.775
730
KRT006 Keratoconjunctivitis 53 0.775
731
P BLD062 Bile Duct Cancer 69 0.772
732
P SYP003 Syphilis 59 0.768
733
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.762
734
PDT042 Pediatric Hepatocellular Carcinoma 51 0.762
735
PSR001 Psoriatic Arthritis 61 0.761
736
DRY001 Dry Eye Syndrome 49 0.761
737
P PHC003 Pheochromocytoma 70 0.761
738
ADR040 Adrenal Gland Pheochromocytoma 45 0.761
739
CLF027 Cleft Palate, Isolated 64 0.760
740
MCS002 Mucositis 55 0.760
741
P CLL015 Collagen Disease 47 0.760
742
SPP007 Suppression Amblyopia 38 0.752
743
AMB002 Amblyopia 49 0.752
744
CND002 Conduct Disorder 50 0.752
745
PRN019 Perinatal Necrotizing Enterocolitis 60 0.752
746
VSC002 Vascular Dementia 59 0.752
747
c BSL034 Basal Cell Carcinoma 7 25 0.751
748
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.739
749
FLL031 Follicular Adenoma 40 0.736
750
GST037 Gastroparesis 52 0.736
751
AYM001 Ayme-Gripp Syndrome 57 0.734
752
PRT251 Proteinuria, Chronic Benign 58 0.733
753
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.733
754
CMM005 Common Cold 55 0.733
755
BLD131 Bladder Urothelial Carcinoma 59 0.727
756
c HPT007 Hepatitis E 50 0.727
757
DSS032 Disease by Infectious Agent 55 0.726
758
PRS025 Presbyopia 39 0.718
759
IRN002 Iron Metabolism Disease 56 0.718
760
c BCT013 Bacterial Pneumonia 47 0.718
761
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.718
762
CHR103 Charge Syndrome 65 0.718
763
P PRK057 Parkinson Disease, Late-Onset 79 0.716
764
BRN024 Bronchitis 67 0.716
765
MNT002 Mental Depression 56 0.713
766
ADN018 Adenoma 58 0.710
767
BRN071 Brain Injury 50 0.710
768
P NGH001 Night Blindness 52 0.708
769
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.708
770
ANR010 Aneurysm of Sinus of Valsalva 30 0.706
771
c CTR110 Cataract 26, Multiple Types 26 0.699
772
HPT046 Hepatic Veno-Occlusive Disease 54 0.699
773
P FML187 Familial Hypertension 34 0.699
774
P SCH015 Schizophrenia 74 0.693
775
GST019 Gastrointestinal Stromal Tumor 78 0.690
777
PRV004 Periventricular Leukomalacia 52 0.689
778
VSC003 Visceral Leishmaniasis 54 0.689
779
MYC013 Mycobacterium Abscessus 42 0.689
780
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.682
781
c BSL024 Basal Cell Carcinoma 1 55 0.682
782
RMB001 Rombo Syndrome 29 0.682
783
P TRC095 Trichoepithelioma, Multiple Familial, 1 34 0.682
784
BSL044 Basal Cell Carcinoma, Infundibulocystic 37 0.682
785
NDL009 Nodular Basal Cell Carcinoma 40 0.682
786
MTT001 Metatypical Basal Cell Carcinoma 32 0.682
787
PGM002 Pigmented Basal Cell Carcinoma 31 0.682
788
ANL013 Anal Margin Basal Cell Carcinoma 18 0.682
789
SBC013 Sebaceous Basal Cell Carcinoma 13 0.682
790
MCR016 Micronodular Basal Cell Carcinoma 35 0.682
791
ADM002 Adamantinoid Basal Cell Epithelioma 20 0.682
792
CLR015 Clear Cell Basal Cell Carcinoma 41 0.682
793
ADN015 Adenoid Basal Cell Carcinoma 32 0.682
794
CYS004 Cystic Basal Cell Carcinoma 37 0.682
795
SRC003 Sarcomatoid Basal Cell Carcinoma 29 0.682
796
SGN001 Signet Ring Basal Cell Carcinoma 34 0.682
797
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.682
798
LNR004 Linear Porokeratosis 34 0.682
799
SPS057 Spasticity 43 0.679
800
c DMN023 Diamond-Blackfan Anemia 1 68 0.678
801
P EMR001 Emery-Dreifuss Muscular Dystrophy 62 0.678
802
BRN056 Bronchopulmonary Dysplasia 57 0.678
803
CCN001 Cocaine Dependence 47 0.678
804
P MYC008 Myocarditis 59 0.675
805
TRM010 Traumatic Brain Injury 50 0.672
806
P HYP061 Hypertrophic Cardiomyopathy 68 0.668
807
BTT016 Batten-Turner Congenital Myopathy 54 0.667
808
P MLN069 Melanoma, Uveal 59 0.667
809
P THR015 Thrombophilia 51 0.667
810
INS001 Insulinoma 59 0.667
811
ATR057 Atrioventricular Block 54 0.665
812
HYP056 Hypoglycemia 65 0.657
813
SHR107 Short Stature-Obesity Syndrome 25 0.655
814
c ALP036 Alopecia, Androgenetic, 2 16 0.655
815
c SPR162 Spermatogenic Failure 50 42 0.655
816
P TRT019 Torticollis 47 0.655
817
MTN003 Motion Sickness 50 0.655
818
OCL004 Ocular Hyperemia 24 0.655
819
LCR009 Lacrimal Gland Adenocarcinoma 22 0.655
820
CRY005 Cryptococcosis 61 0.655
821
P RNG032 Ring Chromosome 39 0.655
822
THY123 Thyroid Gland Follicular Carcinoma 53 0.651
823
c RNG019 Ring Chromosome 3 19 0.650
824
P ESP024 Esophagitis 60 0.650
825
P RTN018 Retinal Disease 53 0.650
826
P INF038 Influenza 68 0.650
827
PHR003 Pharyngitis 57 0.647
828
IFP003 Ifap Syndrome 2 41 0.642
829
CHK001 Chikungunya 60 0.642
830
DRM011 Dermatophytosis 52 0.642
831
P PLY018 Polycythemia 56 0.642
832
P ATX030 Ataxia-Telangiectasia 80 0.635
833
c 46X051 46,xy Sex Reversal 1 38 0.629
834
SPN019 Spondylolisthesis 51 0.629
835
P NNS072 Nonsyndromic Hearing Loss 42 0.629
836
DRG003 Drug Dependence 46 0.629
837
c PRC016 Pre-Eclampsia 64 0.624
838
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.622
839
NNS002 Nonspecific Interstitial Pneumonia 42 0.620
840
P GLM007 Glomerulonephritis 59 0.620
841
CRV038 Cervical Squamous Cell Carcinoma 56 0.618
842
RHM028 Rheumatic Heart Disease 55 0.616
843
CYS008 Cystic Echinococcosis 57 0.614
844
GLC003 Glucose Intolerance 53 0.613
845
c EXD008 Exudative Vitreoretinopathy 1 71 0.605
846
c BRN108 Branchiootic Syndrome 1 63 0.605
847
c TYP008 Type 1 Diabetes Mellitus 77 0.605
848
CNN005 Connective Tissue Disease 66 0.605
849
P UVT001 Uveitis 57 0.601
850
SBV001 Subvalvular Aortic Stenosis 31 0.601
851
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.599
852
CHR682 Chronic Bilirubin Encephalopathy 37 0.599
853
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.598
854
c CHR658 Charcot-Marie-Tooth Disease, Recessive Intermediate a 38 0.598
855
OPP004 Oppositional Defiant Disorder 48 0.598
856
P EHL001 Ehlers-Danlos Syndrome 57 0.598
857
STL001 St. Louis Encephalitis 38 0.598
858
ADV004 Adverse Events of 5-Alpha-Reductase Inhibitors 10 0.598
859
PRP027 Peripheral Vascular Disease 71 0.597
860
P MJR001 Major Depressive Disorder 68 0.597
861
GST045 Gastroenteritis 58 0.593
862
SCT005 Scott Syndrome 51 0.593
863
P SJG008 Sjogren Syndrome 60 0.593
864
INC002 Inclusion Body Myositis 56 0.593
865
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.585
866
c ACT071 Acute Kidney Failure 60 0.581
867
MDD011 Mood Disorder 61 0.581
868
GLL008 Gilles De La Tourette Syndrome 64 0.579
869
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 50 0.579
870
P MXL015 Maxillary Sinusitis 37 0.579
871
c ACT059 Acute Maxillary Sinusitis 35 0.579
872
INT010 Intracranial Embolism 48 0.579
873
P THY054 Thyrotoxic Periodic Paralysis 51 0.579
874
P PRD021 Periodic Paralysis 42 0.579
875
c FML001 Familial Atrial Fibrillation 65 0.578
876
MTB004 Metabolic Acidosis 48 0.577
877
CMB007 Combined Immunodeficiency 56 0.572
878
STT001 Status Epilepticus 58 0.572
879
P TTR001 Tetralogy of Fallot 69 0.568
880
ART017 Aortic Disease 49 0.564
881
MRK001 Merkel Cell Carcinoma 64 0.562
882
P VSC011 Vasculitis 61 0.560
883
c CRN174 Coronary Heart Disease 2 19 0.557
884
c EMR020 Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive 44 0.557
885
ANH001 Ainhum 31 0.557
886
P HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 49 0.557
887
P ESS003 Essential Thrombocythemia 68 0.557
888
PLM031 Poliomyelitis 62 0.557
889
ALV002 Alveolar Echinococcosis 56 0.557
890
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.557
891
IRN008 Iron Overload in Africa 50 0.557
892
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.557
893
RJS001 Ruijs-Aalfs Syndrome 47 0.557
894
ADL096 Adult Hepatocellular Carcinoma 60 0.557
895
HPT079 Hepatoid Adenocarcinoma 39 0.557
896
FBR086 Fibrolamellar Carcinoma 59 0.557
897
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.557
898
OVR062 Ovary Serous Adenocarcinoma 25 0.557
899
PTY007 Pityriasis Rotunda 27 0.557
900
GST033 Gestational Diabetes 60 0.556
902
P ORT004 Orthostatic Intolerance 61 0.551
903
P FBR017 Fibrosarcoma 55 0.551
904
RHM001 Rheumatic Fever 59 0.551
905
SDD001 Sudden Infant Death Syndrome 60 0.547
906
PNG002 Pain Agnosia 51 0.534
907
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.534
908
P SNS001 Sensorineural Hearing Loss 60 0.534
909
P NPH012 Nephrotic Syndrome 61 0.534
910
P ANT088 Anterior Segment Dysgenesis 54 0.529
911
HMN047 Human Cytomegalovirus Infection 59 0.529
912
SVR001 Severe Acute Respiratory Syndrome 68 0.529
913
c ACT068 Acute Cystitis 60 0.529
914
CRN270 Coronary Artery Dissection, Spontaneous 33 0.529
915
PLY001 Polycythemia Vera 69 0.529
916
RTN006 Retinal Drusen 34 0.529
917
ATY022 Atypical Coarctation of Aorta 36 0.529
918
PSD026 Pseudoainhum 25 0.529
919
DSC003 Discrete Subaortic Stenosis 22 0.525
920
HYP781 Hypoascorbemia 52 0.521
921
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.521
922
ATX019 Ataxia with Vitamin E Deficiency 44 0.521
923
P OVR096 Overlap Myositis 27 0.521
924
c ALB010 Albinism, Oculocutaneous, Type Ib 52 0.521
925
CNJ018 Conjunctival Squamous Cell Carcinoma 42 0.521
926
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.521
927
VGN017 Vaginal Cancer 58 0.521
928
DST001 Distal Biliary Tract Carcinoma 24 0.521
929
CRD137 Cardiogenic Shock 56 0.520
930
BRT054 Brittle Bone Disorder 74 0.516
931
c ACT249 Acute Asthma 40 0.516
932
PRT058 Pure Autonomic Failure 58 0.511
933
PPL052 Papillomatosis, Confluent and Reticulated 34 0.506
934
c AXN009 Axenfeld-Rieger Syndrome, Type 1 48 0.502
935
CHR710 Chronic Spontaneous Urticaria 45 0.502
936
P ART005 Arteriovenous Malformation 64 0.502
937
SNS003 Sensory Peripheral Neuropathy 51 0.497
938
P SCK005 Sickle Cell Disease 56 0.497
939
RSP006 Respiratory System Disease 51 0.493
940
KRT001 Keratoconjunctivitis Sicca 49 0.493
941
P GRF003 Graft-Versus-Host Disease 71 0.492
942
P CYS018 Cystitis 58 0.492
943
P ATR010 Atrial Heart Septal Defect 58 0.492
944
THY124 Thyroid Gland Papillary Carcinoma 38 0.491
945
CHG001 Chagas Disease 65 0.487
946
c CHR711 Chronic Asthma 41 0.482
947
P PLY014 Polycystic Kidney Disease 71 0.482
948
IDP011 Idiopathic Interstitial Pneumonia 59 0.482