Search results for POLI

3058 hits were found for POLI

# Family MCID Name MIFTS Score
1
FBL008 Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly 43 27.755
2
XRD010 Xeroderma Pigmentosum, Variant Type 72 15.490
3
MTH009 Mouth Disease 57 13.548
4
HLX001 Helix Syndrome 47 11.438
5
c MYP123 Myopathy, Centronuclear, 1 53 10.651
6
GRG001 Greig Cephalopolysyndactyly Syndrome 64 10.199
7
P MGL030 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 46 9.500
8
49X001 49, Xxxxx 27 9.449
9
DSS008 Disease of Mental Health 74 8.768
10
P DYS007 Dyskeratosis Congenita 66 8.682
11
SLP001 Sleeping Sickness 56 8.580
12
STT041 Stuttering 52 8.189
13
P DMN001 Diamond-Blackfan Anemia 73 8.071
14
RDN001 Reading Disorder 40 7.942
15
PHB003 Phobia, Specific 44 7.898
16
DYS009 Dysthymic Disorder 51 7.689
17
IMM085 Immunodeficiency 25 38 7.532
18
FRS001 Far Eastern Spotted Fever 24 7.532
19
P TRC072 Treacher Collins Syndrome 1 62 7.532
20
EPT024 Epithelial-Stromal Tgfbi Dystrophy 17 7.532
21
MLT010 Multiple Personality Disorder 29 7.532
22
END043 Endometrial Stromal Tumor 34 7.532
23
P LTT001 Lattice Corneal Dystrophy 30 7.532
24
END031 Endometrial Stromal Sarcoma 45 7.532
25
P OVR042 Ovarian Cancer 88 6.773
26
GLB002 Glioblastoma 67 6.399
27
GLL048 Glial Tumor 52 6.247
28
GLM045 Glioma 62 6.215
29
P BRS047 Breast Cancer 97 6.179
30
RPD005 Rapidly Involuting Congenital Hemangioma 48 6.172
31
P LTR001 Lateral Sclerosis 58 4.994
32
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.964
33
P PNC035 Pancreatic Cancer 86 4.903
34
P MLN008 Melanoma 75 4.746
35
OST159 Osteogenic Sarcoma 66 4.697
36
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.682
37
HRW001 Hair Whorl 35 4.660
38
VCC001 Vaccinia 49 4.642
39
P PRS040 Prostate Cancer 95 4.604
40
STM007 Stomatitis 52 4.472
41
P NRB001 Neuroblastoma 66 4.407
42
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.249
43
P HRP006 Herpes Simplex 65 4.096
44
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 4.062
45
P CLR023 Colorectal Cancer 100 4.011
46
P HPT023 Hepatocellular Carcinoma 95 3.993
47
P HNT016 Huntington Disease 73 3.953
48
OCL008 Oculopharyngeal Muscular Dystrophy 53 3.914
49
AGN016 Aging 54 3.896
50
HMN044 Human Immunodeficiency Virus Type 1 76 3.834
51
BCT022 Bacterial Infectious Disease 56 3.811
52
P INF038 Influenza 68 3.788
53
P GLM040 Glioma Susceptibility 1 70 3.741
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.701
55
HGH043 High Grade Glioma 46 3.686
56
CYT002 Cytokine Deficiency 43 3.659
57
P LNG032 Lung Cancer 98 3.631
58
FRN006 Frontotemporal Dementia 68 3.629
59
ISC004 Ischemia 61 3.626
60
48X005 48,xyyy 39 3.622
61
TTN003 Tetanus 64 3.600
62
P BCL017 B-Cell Lymphoma 57 3.583
63
CRB004 Cerebral Artery Occlusion 46 3.479
64
c LKM061 Leukemia, Acute Myeloid 83 3.410
65
SPN186 Spinal Cord Injury 61 3.401
66
OST017 Osteomyelitis 63 3.285
67
PLY150 Polykaryocytosis Inducer 29 3.272
68
P MSC005 Muscular Dystrophy 66 3.245
69
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.239
70
P LKM002 Leukemia 66 3.236
71
SRC014 Sarcoma 64 3.230
72
SPN035 Spindle Cell Sarcoma 51 3.227
73
P MYC084 Mycobacterium Tuberculosis 1 68 3.196
74
HYP266 Hypoxia 56 3.150
75
c HPT073 Hepatitis C Virus 71 3.146
76
ALL029 Allergic Disease 61 3.109
77
TLN003 Telangiectasis 51 3.102
78
P ATX030 Ataxia-Telangiectasia 80 3.099
79
NWC001 Newcastle Disease 48 3.098
80
c SYS001 Systemic Lupus Erythematosus 86 3.095
81
MLG169 Malignant Astrocytoma 57 3.083
82
HND015 Hand Skill, Relative 29 3.074
83
OVR094 Ovarian Epithelial Cancer 39 3.045
84
SVR004 Severe Combined Immunodeficiency 71 3.037
85
P GST053 Gastric Cancer 82 3.029
86
P HPT021 Hepatitis 68 3.019
87
c HPT016 Hepatitis B 62 3.015
88
c SML038 Small Cell Cancer of the Lung 69 3.013
89
P RHN004 Rhinitis 57 2.985
90
P LNG064 Lung Cancer Susceptibility 3 70 2.976
91
P ADN016 Adenocarcinoma 63 2.964
92
CRV035 Cervical Cancer 72 2.953
93
P MYL006 Myeloid Leukemia 60 2.951
94
c HPT003 Hepatitis a 63 2.947
95
BNR002 Bone Resorption Disease 47 2.921
96
c PCH010 Pachyonychia Congenita 3 43 2.920
97
P ART022 Arthritis 70 2.901
98
P BRS044 Breast Adenocarcinoma 58 2.895
99
DPH001 Diphtheria 59 2.869
100
P PRD008 Periodontitis 64 2.868
101
P PHC003 Pheochromocytoma 70 2.868
102
ADR040 Adrenal Gland Pheochromocytoma 45 2.850
103
INT323 Intraocular Pressure Quantitative Trait Locus 63 2.845
104
CHL014 Cholera 62 2.843
105
HYP066 Hyperglycemia 60 2.828
106
P ENC004 Encephalitis 61 2.804
107
BRN028 Brain Cancer 73 2.800
108
P LPS004 Lupus Erythematosus 61 2.787
109
PRT036 Peritonitis 65 2.786
110
TRM010 Traumatic Brain Injury 50 2.781
111
SQM006 Squamous Cell Carcinoma 59 2.764
112
P LKM071 Leukemia, Chronic Lymphocytic 74 2.745
113
ACT098 Acute Erythroid Leukemia 55 2.741
114
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.740
115
IMM167 Immune Deficiency Disease 77 2.729
116
MYL069 Myeloma, Multiple 77 2.728
117
c HPT001 Hepatitis C 61 2.708
118
BRN071 Brain Injury 50 2.703
119
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.699
120
ANT024 Anthrax Disease 58 2.687
121
CHD004 Chudley-Mccullough Syndrome 47 2.574
122
P PNC044 Pancreatitis 61 2.570
123
47X002 47,xyy 48 2.566
124
P NRP001 Neuropathy 59 2.566
125
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 2.558
126
RNL114 Renal Cell Carcinoma, Nonpapillary 79 2.557
127
ALL003 Allergic Rhinitis 66 2.546
128
P BLD134 Bladder Cancer 79 2.539
129
P SBS003 Substance Abuse 54 2.530
130
MDD018 Middle East Respiratory Syndrome 44 2.502
131
ESP021 Esophageal Cancer 84 2.496
132
P SPP010 Suppressor of Tumorigenicity 3 51 2.485
133
KRT019 Keratitis, Hereditary 66 2.463
134
TCK001 Tick-Borne Encephalitis 59 2.452
135
OST012 Osteoarthritis 77 2.450
136
P LYM118 Lymphoma 69 2.448
137
ATM095 Autoimmune Disease 61 2.430
138
PPL052 Papillomatosis, Confluent and Reticulated 34 2.369
139
TXC005 Toxic Shock Syndrome 62 2.365
140
P SKN015 Skin Carcinoma 71 2.357
141
BRK010 Burkitt Lymphoma 66 2.353
142
P SCH015 Schizophrenia 74 2.338
143
P PLM036 Pulmonary Fibrosis 65 2.337
144
DBT010 Diabetic Neuropathy 54 2.329
145
CHL065 Cholangiocarcinoma 58 2.328
146
INT079 Intrahepatic Cholangiocarcinoma 51 2.324
147
P KLZ004 Kala-Azar 1 41 2.308
148
LSH001 Leishmaniasis 63 2.308
149
P FBR017 Fibrosarcoma 55 2.304
150
c ACT027 Acute Pancreatitis 60 2.285
151
CHR100 Chronic Ulcer of Skin 57 2.274
152
P PLY006 Polydactyly 58 2.257
153
SKN016 Skin Disease 62 2.254
154
CLN015 Colon Adenocarcinoma 64 2.250
155
P MDL005 Medulloblastoma 75 2.244
156
VRL011 Viral Infectious Disease 60 2.241
157
PNC129 Pancreatic Adenocarcinoma 65 2.239
158
P PLY011 Polycystic Ovary Syndrome 57 2.236
159
c TYP009 Type 2 Diabetes Mellitus 92 2.235
160
P THR014 Thrombocytopenia 66 2.213
161
CHR066 Chronic Fatigue Syndrome 60 2.210
162
P ACN011 Acne 55 2.199
163
ALL014 Allergic Encephalomyelitis 34 2.193
164
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.188
165
PRT037 Pertussis 49 2.182
166
P BNG032 Benign Mesothelioma 53 2.180
167
c MCR115 Microvascular Complications of Diabetes 5 65 2.169
168
P DBT009 Diabetes Mellitus 67 2.140
169
P ALZ034 Alzheimer Disease 87 2.134
170
P VSC007 Vascular Disease 62 2.134
171
CYS001 Cystic Fibrosis 77 2.130
172
DSS032 Disease by Infectious Agent 55 2.128
173
INS024 Insulin-Like Growth Factor I 77 2.125
174
SKN019 Skin Melanoma 70 2.125
175
P NTR004 Neutropenia 62 2.117
176
CLT003 Colitis 63 2.100
177
PPL022 Papilloma 53 2.096
178
P CNJ013 Conjunctivitis 66 2.095
179
P THL005 Thalassemia 56 2.074
180
P EYD002 Eye Disease 57 2.069
181
c JVN010 Juvenile Rheumatoid Arthritis 66 2.048
182
TRT001 Teratocarcinoma 41 2.033
183
P LKM062 Leukemia, Acute Lymphoblastic 69 2.026
184
c ATS007 Autism Spectrum Disorder 72 2.025
185
IRN002 Iron Metabolism Disease 56 2.018
186
MXD026 Mixed Glioma 45 2.017
187
SQM002 Squamous Cell Papilloma 45 2.014
188
P PRK039 Parkinsonism 55 2.014
189
LNG099 Lung Disease 62 1.995
190
RBS001 Rabies 58 1.994
191
ENP001 Enophthalmos 40 1.992
192
MYL009 Myelodysplastic Syndrome 67 1.988
193
URT049 Urate Oxidase, Pseudogene 24 1.975
194
P NSP012 Nasopharyngeal Carcinoma 60 1.975
195
P ADL010 Adult Respiratory Distress Syndrome 71 1.974
196
PRR019 Perioral Myoclonia with Absences 27 1.968
197
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.965
198
EWN003 Ewing Sarcoma 70 1.955
200
P PLY019 Polyneuropathy 53 1.937
201
ARG004 Argyria 26 1.936
202
P OVR082 Overgrowth Syndrome 42 1.920
203
P CND004 Candidiasis 57 1.917
204
CHL123 Chlamydia 58 1.917
205
P RTN024 Retinoblastoma 72 1.911
206
AVN001 Avian Influenza 61 1.908
207
LYM019 Lymphosarcoma 46 1.902
208
INS001 Insulinoma 59 1.899
209
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.894
210
END057 Endometrial Cancer 71 1.887
211
P RTN018 Retinal Disease 53 1.885
212
EMB004 Embryonal Carcinoma 55 1.869
213
P RHM011 Rheumatoid Arthritis 81 1.867
214
DRM006 Dermatitis 62 1.858
215
P ANR048 Aniridia 1 66 1.839
216
ORL015 Oral Squamous Cell Carcinoma 43 1.832
217
ALC007 Alcohol Dependence 65 1.830
218
NRR001 Neuroretinitis 42 1.830
219
P MYC007 Myocardial Infarction 69 1.830
220
RTN023 Retinitis 45 1.830
221
DWN001 Down Syndrome 70 1.827
222
SYN007 Synovitis 54 1.820
223
PLC002 Plica Syndrome 35 1.820
224
P PLY041 Polymyositis 59 1.820
225
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.814
226
P INF037 Inflammatory Bowel Disease 53 1.808
227
P UVT001 Uveitis 57 1.804
228
P MTR014 Motor Neuron Disease 65 1.793
229
P SYS005 Systemic Scleroderma 73 1.789
230
P AST005 Asthma 76 1.789
231
AZS001 Azoospermia 45 1.784
232
P RTN016 Retinal Degeneration 52 1.782
233
P MSC003 Muscular Atrophy 52 1.772
234
THY029 Thyroid Carcinoma 54 1.770
235
P ALC033 Alcohol Use Disorder 67 1.752
236
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.752
237
KPS004 Kaposi Sarcoma 76 1.749
238
WRN001 Werner Syndrome 69 1.748
239
P MLN007 Male Infertility 56 1.748
240
BRC012 Brucellosis 66 1.734
241
PST028 Post-Traumatic Stress Disorder 59 1.727
242
P CTR002 Cataract 59 1.723
243
ORL011 Oral Cancer 60 1.722
244
LWG006 Low Grade Glioma 41 1.709
245
c MCR133 Microvascular Complications of Diabetes 4 41 1.700
246
c MCR113 Microvascular Complications of Diabetes 3 52 1.700
247
c MCR130 Microvascular Complications of Diabetes 6 41 1.700
248
c MCR120 Microvascular Complications of Diabetes 7 47 1.700
249
c PRG020 Paragangliomas 3 39 1.698
250
FTT001 Fatty Liver Disease 61 1.689
251
PST092 Posttransplant Acute Limbic Encephalitis 29 1.689
252
ATH013 Atherosclerosis Susceptibility 63 1.687
253
P INF032 Infertility 60 1.682
254
DFC004 Deficiency Anemia 74 1.679
255
P DRM053 Dermatitis, Atopic 65 1.679
256
SVR001 Severe Acute Respiratory Syndrome 68 1.678
257
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.675
258
PST011 Pustulosis of Palm and Sole 52 1.672
259
MNT002 Mental Depression 56 1.671
260
NCL008 Nuclear Ribonucleic Acid 15 1.668
261
P PRN023 Prion Disease 60 1.667
262
ALL006 Allergic Asthma 56 1.663
263
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.653
264
RTN017 Retinal Detachment 60 1.652
265
PLS011 Plasmacytoma 56 1.649
266
ULN017 Ulna and Fibula, Absence of, with Severe Limb Deficiency 35 1.646
267
DPR016 Depression 65 1.637
268
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.636
269
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.636
270
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.636
271
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.636
272
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.636
273
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.636
274
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.636
275
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.636
276
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.636
277
P PRP019 Peripheral Nervous System Disease 57 1.630
278
c TYP008 Type 1 Diabetes Mellitus 77 1.627
279
ADN018 Adenoma 58 1.621
280
P HRT032 Heart Disease 84 1.621
281
ATS010 Autosomal Recessive Disease 42 1.606
282
c MST023 Mesothelioma, Malignant 56 1.601
283
P TMR010 Tumor Predisposition Syndrome 69 1.598
284
THR024 Thrombosis 56 1.595
285
c HYP836 Hypercholesterolemia, Familial, 1 73 1.593
286
P GLM007 Glomerulonephritis 59 1.585
287
VSC003 Visceral Leishmaniasis 54 1.583
288
P ENC018 Encephalopathy 62 1.583
289
ART140 Arteries, Anomalies of 52 1.582
290
P CRD119 Cardiac Arrest 68 1.576
291
c ACT071 Acute Kidney Failure 60 1.576
292
HMP009 Haemophilus Influenzae 41 1.574
293
LYM027 Lymphopenia 56 1.568
294
c BLD140 Blood Group, I System 47 1.561
295
LPD008 Lipid Metabolism Disorder 61 1.560
296
P HYP098 Hypereosinophilic Syndrome 66 1.555
297
P RTN008 Retinitis Pigmentosa 79 1.555
298
P PRK057 Parkinson Disease, Late-Onset 79 1.555
299
c SCL052 Scleroderma, Familial Progressive 60 1.547
300
P END047 Endophthalmitis 53 1.540
301
CHC001 Chickenpox 56 1.533
302
P DRM010 Dermatomyositis 61 1.529
303
CLF001 Cleft Lip 54 1.524
304
P CRN300 Coronary Heart Disease 1 73 1.523
305
HPT022 Hepatoblastoma 54 1.520
306
CHG001 Chagas Disease 65 1.520
307
IMP005 Impotence 52 1.519
308
c BTT014 Beta-Thalassemia 72 1.512
309
P PTS002 Ptosis 52 1.511
310
BRN032 Brain Glioma 45 1.505
311
PRM329 Premature Aging 36 1.498
312
P PSR002 Psoriasis 63 1.497
313
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 1.493
314
INH023 Inherited Cancer-Predisposing Syndrome 53 1.493
315
P DNG005 Dengue Virus 55 1.492
316
ACT119 Acute Promyelocytic Leukemia 62 1.483
317
LRY018 Laryngeal Squamous Cell Carcinoma 47 1.483
318
PNM008 Pneumothorax 54 1.474
319
c OVR114 Ovarian Cancer 1 60 1.470
320
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.469
321
CLF004 Cleft Lip/palate 57 1.467
322
P PLY147 Polydactyly, Postaxial, Type A1 50 1.466
323
P GST044 Gastritis 55 1.463
324
P BND020 Bone Disease 60 1.461
325
P DMN002 Dementia 65 1.458
326
P GRF003 Graft-Versus-Host Disease 71 1.454
327
SML019 Smallpox 55 1.453
328
CMB007 Combined Immunodeficiency 56 1.448
329
JPN002 Japanese Encephalitis 61 1.448
330
P THY023 Thymoma 64 1.448
331
c THY107 Thymoma, Familial 42 1.448
332
P DRR001 Diarrhea 55 1.446
333
LPP008 Lipoprotein Quantitative Trait Locus 65 1.442
334
CNG034 Congestive Heart Failure 69 1.442
335
CLR030 Clear Cell Renal Cell Carcinoma 54 1.441
336
c ACT134 Acute Liver Failure 57 1.437
337
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.432
338
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.429
339
SCH014 Schistosomiasis 56 1.429
340
CRV002 Cervix Uteri Carcinoma in Situ 48 1.426
341
CRV045 Cervical Intraepithelial Neoplasia 38 1.426
342
P INS002 in Situ Carcinoma 53 1.413
343
P MYC008 Myocarditis 59 1.410
344
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 1.410
345
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.404
346
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.401
347
c ACT073 Acute Leukemia 59 1.401
348
DNT008 Denture Stomatitis 35 1.398
349
CLR109 Colorectal Adenocarcinoma 50 1.396
350
PLR008 Pleurisy 49 1.396
351
P MNC007 Monocytic Leukemia 48 1.391
352
c ALP101 Alpha-Thalassemia 62 1.390
353
c VRL010 Viral Hepatitis 52 1.388
354
STR067 Stroke, Ischemic 79 1.387
355
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.383
356
GLS001 Gliosarcoma 63 1.383
357
MLR004 Malaria 78 1.381
358
P PNM007 Pneumonia 64 1.381
359
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.381
360
c LKM005 Leukemia, T-Cell, Chronic 33 1.379
361
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.375
362
PRP027 Peripheral Vascular Disease 71 1.375
363
LMB062 Limb Ischemia 55 1.375
364
P PRS038 Personality Disorder 65 1.360
365
BRN004 Brain Edema 54 1.355
366
c FNC027 Fanconi Anemia, Complementation Group a 81 1.352
367
ABD010 Abdominal Wall Defect 39 1.349
368
P BNC003 Bone Cancer 58 1.343
369
P KDN018 Kidney Disease 72 1.343
370
DGN001 Degenerative Disc Disease 48 1.342
371
P TXP001 Toxoplasmosis 60 1.332
372
P ESP024 Esophagitis 60 1.332
373
CNT047 Contact Dermatitis 57 1.327
374
PRT251 Proteinuria, Chronic Benign 58 1.323
375
MSL001 Measles 61 1.321
376
P ALP008 Alopecia 53 1.321
377
MST004 Mast Cell Neoplasm 41 1.318
378
P MLT020 Multiple Sclerosis 79 1.313
379
EXT007 Extracutaneous Mastocytoma 38 1.313
380
P BNG030 Benign Ependymoma 51 1.312
381
CLL010 Cellular Ependymoma 58 1.312
382
ALL010 Allergic Contact Dermatitis 56 1.309
383
P OST002 Osteoporosis 77 1.308
384
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.308
385
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.308
386
GLC003 Glucose Intolerance 53 1.300
387
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.296
388
c PLY136 Polydactyly, Preaxial I 32 1.290
389
PLY024 Polymicrogyria 46 1.290
390
P CCK001 Cockayne Syndrome 68 1.284
391
P FML011 Familial Adenomatous Polyposis 71 1.282
392
P LVR013 Liver Disease 68 1.282
393
OST016 Osteochondrosis 52 1.277
394
P OST009 Osteochondritis Dissecans 61 1.277
395
SLC006 Silicosis 55 1.271
396
P MYP004 Myopathy 67 1.269
397
ACQ007 Acquired Immunodeficiency Syndrome 58 1.265
398
MSC157 Muscular Dystrophy, Duchenne Type 79 1.265
399
SPL018 Splenomegaly 47 1.265
400
GST040 Gastric Adenocarcinoma 66 1.265
401
P MCH002 Machado-Joseph Disease 63 1.260
402
PTT037 Pituitary Tumors 44 1.254
403
HYP056 Hypoglycemia 65 1.254
404
FLL027 Fallopian Tube Carcinoma 66 1.253
405
MNT001 Mantle Cell Lymphoma 65 1.248
406
VRL003 Variola Major 43 1.244
407
OST003 Osteonecrosis 61 1.242
408
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 1.239
409
GST045 Gastroenteritis 58 1.237
410
DNT012 Dental Caries 53 1.237
411
PNC085 Penicillin Allergy 43 1.234
412
RHB024 Rhabdomyosarcoma 2 65 1.230
413
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.230
414
DRY001 Dry Eye Syndrome 49 1.228
415
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.228
416
c LKM063 Leukemia, Chronic Myeloid 71 1.228
417
P CLC063 Celiac Disease 1 66 1.226
418
P HYP086 Hypothyroidism 69 1.221
419
P ANP001 Anaplastic Large Cell Lymphoma 61 1.218
420
OVR059 Ovary Adenocarcinoma 49 1.218
421
WST005 West Nile Virus 55 1.212
422
P ATS364 Autism 72 1.211
423
P CHR345 Chronic Pain 50 1.206
424
c BRS111 Breast-Ovarian Cancer, Familial 2 54 1.200
425
P PLV020 Pelvic Organ Prolapse 58 1.199
426
AVD001 Avoidant Personality Disorder 49 1.199
427
c HYP595 Hypertension, Essential 84 1.190
428
SWN001 Swine Influenza 45 1.190
429
c BSL007 Basal Cell Carcinoma 68 1.186
430
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 50 1.186
431
IGG001 Iga Glomerulonephritis 50 1.184
432
BRN024 Bronchitis 67 1.180
433
ACT003 Acute Kidney Tubular Necrosis 46 1.180
434
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.173
435
MST005 Mastitis 52 1.165
436
HMS001 Hemosiderosis 48 1.165
437
ANR040 Aneurysm 60 1.165
438
P RRH023 Rare Hereditary Hemochromatosis 53 1.165
439
IDP069 Idiopathic Avascular Necrosis 23 1.162
440
P EXN002 Exanthem 58 1.162
441
PRS045 Prostatic Hypertrophy 52 1.162
442
ANT039 Antisynthetase Syndrome 55 1.160
443
PLM031 Poliomyelitis 62 1.158
444
P HMN010 Hemangioma 61 1.158
445
P MYS005 Myositis 56 1.157
446
SCR011 Scrapie 39 1.156
447
CNN005 Connective Tissue Disease 66 1.153
448
P CRN037 Craniosynostosis 67 1.150
449
c SPR009 Sporadic Breast Cancer 42 1.150
450
ULC004 Ulcerative Colitis 74 1.148
451
P TRN020 Turner Syndrome 67 1.145
452
PRS021 Prostatic Adenoma 43 1.144
453
P HML002 Hemolytic Anemia 62 1.144
454
P MCR129 Microvascular Complications of Diabetes 1 68 1.140
455
DMY004 Demyelinating Disease 50 1.138
456
SFT003 Soft Tissue Sarcoma 57 1.136
457
HYP060 Hyperinsulinism 53 1.135
458
CWP001 Cowpox 44 1.132
459
c ACT068 Acute Cystitis 61 1.128
460
P CRN026 Corneal Edema 42 1.127
461
P EPD016 Epidermolysis Bullosa 53 1.127
462
FNG016 Fungal Keratitis 39 1.127
463
CCC001 Coccidioidomycosis 58 1.125
464
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.121
465
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.119
466
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.119
467
TBC004 Tobacco Addiction 63 1.119
468
P EPD009 Epidermolysis Bullosa Dystrophica 66 1.119
469
c MJR024 Major Affective Disorder 9 40 1.118
470
c MJR022 Major Affective Disorder 8 37 1.118
471
P BPL003 Bipolar Disorder 56 1.118
472
P ART021 Arteriosclerosis 53 1.114
473
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 1.110
474
LYM143 Lymphoma, Non-Hodgkin, Familial 79 1.107
475
PRS129 Prostatic Hyperplasia, Benign 48 1.106
476
P MMP001 Mumps 56 1.106
477
P ART023 Arthropathy 60 1.106
478
CTN007 Cutaneous Leishmaniasis 61 1.106
479
P OLG002 Oligodendroglioma 66 1.103
480
P EPL164 Epilepsy 70 1.102
481
LVR012 Liver Cirrhosis 62 1.102
482
INT002 Intermittent Claudication 61 1.101
483
P FRG001 Fragile X Syndrome 70 1.099
484
SBS004 Substance Dependence 46 1.099
485
P RHB003 Rhabdomyosarcoma 66 1.097
486
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.092
487
CRN027 Corneal Neovascularization 47 1.092
488
P CHN012 Chondrosarcoma 56 1.086
489
ADL002 Adult Syndrome 69 1.085
490
PRT013 Portal Hypertension 59 1.083
491
DFF005 Diffuse Large B-Cell Lymphoma 55 1.080
492
GT001 Gout 63 1.078
493
P END044 Endometriosis 62 1.075
494
LYM017 Lyme Disease 63 1.074
495
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.071
496
OCL069 Ocular Motor Apraxia 57 1.071
497
CRV040 Cervix Carcinoma 50 1.071
499
AST006 Astigmatism 46 1.069
500
ART002 Arts Syndrome 66 1.069
501
P THY032 Thyroiditis 56 1.064
502
CRB039 Cerebrovascular Disease 65 1.064
503
MLG079 Malignant Pleural Mesothelioma 42 1.058
504
PRS047 Prostatitis 58 1.058
505
P SJG008 Sjogren Syndrome 61 1.056
506
HYP457 Hypertrophic Scars 42 1.054
507
TRC005 Tracheal Stenosis 43 1.054
508
P MYS003 Myasthenia Gravis 68 1.052
509
c ATR087 Atrial Standstill 1 74 1.052
510
P ART005 Arteriovenous Malformation 65 1.048
511
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 1.048
512
P MJR001 Major Depressive Disorder 68 1.046
513
CRH001 Crohn's Disease 80 1.046
514
c VSC019 Vesicoureteral Reflux 1 56 1.043
515
CHK001 Chikungunya 60 1.041
516
CHR074 Choriocarcinoma 46 1.041
517
LYS002 Lysosomal Storage Disease 51 1.040
518
CRT015 Carotid Artery Occlusion 45 1.040
519
KLD004 Keloid Disorder 39 1.040
520
P DBT005 Diabetes Insipidus 54 1.040
521
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.040
522
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.040
523
P URN019 Urinary Tract Infection 49 1.040
524
P VSC011 Vasculitis 61 1.040
525
PLG002 Plague 58 1.036
526
P SPN046 Spinal Muscular Atrophy 62 1.032
527
GST023 Gastric Ulcer 52 1.032
528
TRN015 Transient Cerebral Ischemia 62 1.032
529
HDN002 Head Injury 44 1.032
530
ANP005 Anaplastic Astrocytoma 59 1.031
531
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 1.028
532
P ANT006 Antiphospholipid Syndrome 55 1.024
533
c SPN225 Spondyloarthropathy 1 70 1.021
534
KLB003 Klebsiella Pneumonia 49 1.019
535
INH001 Inhalation Anthrax 41 1.015
536
P HYP750 Hypertriglyceridemia, Familial 62 1.015
537
CHL068 Cholestasis 61 1.014
538
RFT001 Rift Valley Fever 50 1.014
539
P HMP007 Hemophilia 52 1.014
540
INT395 Intracranial Meningioma 48 1.010
541
MNN043 Meningioma, Familial 79 1.010
542
SCR001 Secretory Meningioma 40 1.010
543
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.010
544
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 1.008
545
C9R003 C9orf72 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 11 1.008
546
TRN018 Transitional Cell Carcinoma 56 1.006
547
PLM010 Pulmonary Edema 54 1.006
548
CRV038 Cervical Squamous Cell Carcinoma 56 1.002
549
P NJM001 Nijmegen Breakage Syndrome 75 0.999
550
CHR072 Chordoma 57 0.997
551
CND006 Candida Glabrata 29 0.997
552
MTB004 Metabolic Acidosis 48 0.987
553
NRT004 Neuritis 53 0.987
554
ART109 Arterial Thoracic Outlet Syndrome 24 0.987
555
P PLM037 Pulmonary Hypertension 69 0.987
556
STT001 Status Epilepticus 58 0.987
557
c ACT075 Acute Myocardial Infarction 55 0.987
558
NNL006 Non-Alcoholic Steatohepatitis 54 0.980
559
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.980
560
P TRT010 Teratoma 50 0.980
561
STN013 Stenotrophomonas Maltophilia Infection 26 0.980
562
c BCT007 Bacterial Meningitis 55 0.980
563
P PNM006 Pneumoconiosis 55 0.977
564
ANT018 Anthracosis 51 0.977
565
LMB050 Limbal Stem Cell Deficiency 50 0.977
566
HRN003 Heroin Dependence 44 0.977
567
CVD001 Covid-19 58 0.976
568
P MYT002 Myotonic Dystrophy 51 0.975
569
VNH007 Von Hippel-Lindau Syndrome 73 0.975
570
RTN020 Retinal Vascular Disease 45 0.973
571
P OPT006 Optic Nerve Disease 57 0.967
572
FNG017 Fungal Infectious Disease 54 0.967
573
GNT003 Genital Herpes 54 0.967
574
OCL006 Ocular Hypertension 53 0.967
575
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.965
576
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.965
577
P MYP006 Myopia 55 0.965
578
c HPT007 Hepatitis E 50 0.960
579
PRP080 Peripheral Artery Disease 54 0.958
580
VRC005 Varicose Veins 59 0.956
581
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.956
582
SYN005 Synostosis 43 0.950
583
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.950
584
CLR108 Colorectal Adenoma 63 0.949
585
P KDN017 Kidney Cancer 60 0.947
586
PLY179 Polyomavirus-Associated Nephropathy 25 0.945
587
MTH071 Methane Production 25 0.945
588
PRM013 Premature Menopause 57 0.942
589
CNS004 Constipation 56 0.942
590
P SLP005 Sleep Disorder 62 0.942
591
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.941
592
P VNS003 Venous Insufficiency 54 0.934
593
P LRY044 Larynx Cancer 53 0.934
594
HYP043 Hyperandrogenism 47 0.933
595
NPH009 Nephrolithiasis 54 0.929
596
P SZR006 Seizure Disorder 69 0.929
597
ACT084 Acute Stress Disorder 53 0.925
598
THY030 Thyroid Gland Disease 50 0.925
599
RTN003 Retinal Ischemia 48 0.925
600
BCT002 Bacterial Vaginosis 53 0.920
601
DBT002 Diabetic Autonomic Neuropathy 40 0.918
602
PLM001 Pulmonary Tuberculosis 69 0.917
603
FDL002 Food Allergy 47 0.917
604
TNP004 Tn Polyagglutination Syndrome 42 0.917
605
THY122 Thyroid Gland Cancer 59 0.917
606
DMP001 Dumping Syndrome 43 0.917
607
END086 End Stage Renal Disease 54 0.917
608
c PRS130 Prostate Cancer, Hereditary, 8 32 0.917
609
c PRS136 Prostate Cancer, Hereditary, 6 33 0.917
610
c PRM038 Primary Agammaglobulinemia 47 0.917
611
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.911
612
PSY004 Psychotic Disorder 66 0.911
613
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 0.908
614
P MNN013 Meningitis 65 0.908
615
URT037 Urethral Stricture 42 0.906
616
P LPR021 Leprosy 3 71 0.904
617
LMY002 Leiomyoma 51 0.904
618
P CHL066 Cholangitis 51 0.904
619
HNS001 Hansen's Disease 32 0.904
620
LYM009 Lymphocytic Choriomeningitis 46 0.903
621
ILS001 Ileus 49 0.899
622
HMC014 Homocysteinemia 52 0.899
623
TST044 Testicular Torsion 45 0.899
624
HRT011 Heart Septal Defect 49 0.899
625
PNC034 Pancreas Disease 49 0.899
626
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.898
627
PRM236 Primary Biliary Cholangitis 62 0.898
628
TQP001 Taqi Polymorphism 29 0.891
629
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.891
630
BCK006 Back Pain 43 0.891
631
ENT011 Enterocolitis 55 0.891
632
CNT033 Central Nervous System Cancer 47 0.890
633
P KRT007 Keratoconus 50 0.889
634
PPT005 Peptic Ulcer Disease 58 0.889
635
ANX010 Anxiety 70 0.884
636
CMM005 Common Cold 55 0.884
637
P SYP003 Syphilis 59 0.884
638
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.883
639
P LMY004 Leiomyosarcoma 62 0.879
640
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.878
641
ENT004 Enthesopathy 51 0.878
642
P RCT021 Rectum Cancer 54 0.878
643
INT066 Interstitial Lung Disease 60 0.878
644
MDD011 Mood Disorder 62 0.878
645
HRP004 Herpes Zoster 60 0.878
646
P AMY004 Amyloidosis 69 0.878
647
VNZ002 Venezuelan Equine Encephalitis 46 0.878
648
P CHR285 Chronic Myelomonocytic Leukemia 59 0.876
649
P NRC002 Narcolepsy 55 0.876
650
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.875
651
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.875
652
P ECT006 Ectodermal Dysplasia 62 0.872
653
DWR001 Dwarfism 45 0.872
654
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.871
655
P PLY014 Polycystic Kidney Disease 71 0.871
656
IGR001 Ige Responsiveness, Atopic 59 0.871
657
P VTR007 Vitreoretinopathy 45 0.871
658
P PRS062 Persistent Hyperplastic Primary Vitreous 47 0.869
659
EXS001 Exostosis 49 0.869
660
HYP014 Hyperuricemia 51 0.869
661
LNG039 Lung Squamous Cell Carcinoma 57 0.869
662
PPL002 Papillary Carcinoma 46 0.869
663
c BRN108 Branchiootic Syndrome 1 63 0.858
664
BRN002 Bronchiolitis 57 0.858
665
URM002 Uremia 47 0.858
666
P URT039 Urticaria 57 0.858
667
P SCL018 Scoliosis 57 0.856
668
P TRM003 Tremor 50 0.856
669
P HYP730 Hypogonadotropic Hypogonadism 54 0.856
670
P BRC006 Brachydactyly 52 0.856
671
P OVR046 Ovarian Cyst 44 0.851
672
TYP007 Typhoid Fever 63 0.849
673
P CYS018 Cystitis 59 0.849
674
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.846
675
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.846
676
URT010 Ureteral Obstruction 45 0.846
677
AMN003 Amnestic Disorder 54 0.846
678
CRY005 Cryptococcosis 61 0.846
679
VRC001 Varicocele 48 0.846
680
c PRC016 Pre-Eclampsia 64 0.844
681
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.841
682
P GLL022 Guillain-Barre Syndrome 59 0.841
683
CHR073 Choreatic Disease 53 0.841
684
FLR002 Filariasis 55 0.841
685
c BCT013 Bacterial Pneumonia 47 0.841
686
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.841
687
TTH002 Tooth Agenesis 61 0.837
688
P STR020 Strabismus 56 0.834
689
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.834
690
MCH006 Mechanical Strabismus 40 0.834
691
ANX004 Anoxia 40 0.834
692
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.834
693
HMN047 Human Cytomegalovirus Infection 59 0.833
694
BTT017 Beta-Thalassemia Major 53 0.833
695
MCL006 Macular Retinal Edema 56 0.833
696
NRM005 Neuromuscular Disease 63 0.833
697
P AVS003 Avascular Necrosis 41 0.833
698
LYM133 Lymphoma, Hodgkin, Classic 74 0.826
699
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.825
700
c PRD040 Periodontitis, Chronic 52 0.825
701
P RSP003 Respiratory Failure 74 0.825
702
P HYD006 Hydrocephalus 63 0.825
703
P TRC031 Trichorhinophalangeal Syndrome 37 0.825
704
c SPR119 Spermatogenic Failure, X-Linked, 1 36 0.821
705
LBR035 Liberfarb Syndrome 28 0.821
706
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 39 0.821
707
P LCT001 Lactic Acidosis 50 0.821
708
P LPS002 Liposarcoma 64 0.821
709
c ORF034 Orofaciodigital Syndrome Vi 55 0.821
710
P NRV006 Nervous System Cancer 47 0.820
711
PLL012 Pollen Allergy 44 0.817
712
NNT008 Neonatal Abstinence Syndrome 40 0.817
713
BNN005 Bunion 31 0.817
714
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.814
715
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.812
716
TRC097 Tracheomalacia 43 0.808
717
HPT004 Hepatic Coma 43 0.808
718
DYS073 Dysphagia 53 0.806
719
PSR001 Psoriatic Arthritis 61 0.802
720
c ATM099 Autoimmune Uveitis 44 0.800
721
P END033 Endocarditis 58 0.800
722
c MGR028 Migraine with or Without Aura 1 64 0.800
723
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.800
724
CYT005 Cytomegalovirus Retinitis 50 0.800
725
c DYS173 Dyskeratosis Congenita, Autosomal Recessive 6 28 0.793
726
P CRD246 Cardiovascular System Disease 55 0.793
727
HPT019 Hepatic Encephalopathy 59 0.793
728
PPM002 Ppoma 28 0.793
729
c HMP029 Hemophilia a 69 0.791
730
c VRL005 Viral Pneumonia 52 0.791
731
RNL077 Renal Fibrosis 46 0.791
732
FCT001 Factor Viii Deficiency 62 0.791
733
c DLT002 Dilated Cardiomyopathy 79 0.791
734
MLT006 Multidrug-Resistant Tuberculosis 47 0.791
735
c LRG001 Large Cell Carcinoma 48 0.791
736
c JVN061 Juvenile Arthritis 56 0.791
737
FBL010 Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 24 0.785
738
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.785
739
ODN023 Odontochondrodysplasia 70 0.785
740
AMN014 Aminopterin Syndrome Sine Aminopterin 31 0.782
741
TRY001 Trypanosomiasis 50 0.782
742
MNN009 Meningoencephalitis 48 0.782
743
P OVR049 Ovarian Disease 50 0.782
744
MXD005 Mixed Connective Tissue Disease 57 0.782
746
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.781
747
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.772
748
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.772
749
c HMP004 Hemophilia B 68 0.772
750
P OPN001 Open-Angle Glaucoma 55 0.772
751
CLF027 Cleft Palate, Isolated 64 0.772
752
EST003 Eastern Equine Encephalitis 37 0.772
753
SKN020 Skin Papilloma 40 0.772
754
P RBL001 Rubella 58 0.771
755
P CRV039 Cervicitis 52 0.766
756
P SLP006 Sleep Apnea 69 0.765
757
P LYN001 Lynch Syndrome 76 0.765
758
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.762
759
NRM004 Neuroma 49 0.762
760
LPT001 Leptospirosis 66 0.762
761
PLM033 Pulmonary Embolism 58 0.762
762
P SYN012 Synpolydactyly 38 0.757
763
IMM155 Immune Response to Synthetic Polypeptide--Irphegal 5 0.757
764
MCR013 Microphthalmia 60 0.752
765
MCS002 Mucositis 55 0.752
766
P MLN069 Melanoma, Uveal 59 0.752
767
NRL016 Neural Tube Defects 81 0.752
768
c ACT249 Acute Asthma 40 0.752
769
c ATM113 Autoimmune Cholangitis 30 0.752
770
MYM001 Myoma 54 0.752
771
RYN005 Raynaud Phenomenon 45 0.752
772
PRS115 Prosthetic Joint Infection 42 0.752
773
c PRT136 Proteasome-Associated Autoinflammatory Syndrome 2 21 0.751
774
NVS015 Nevus Comedonicus 38 0.751
775
CTR107 Cataract 13 with Adult I Phenotype 23 0.751
776
BRB002 Barbiturate Dependence 28 0.751
777
c ORF043 Orofaciodigital Syndrome Ix 35 0.751
778
8P2002 8p23.1 Duplication Syndrome 22 0.751
779
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.751
780
P SPS008 Spastic Ataxia 41 0.741
781
DCT002 Ductal Carcinoma in Situ 58 0.741
782
IRT001 Iritis 45 0.741
783
MTC005 Mitochondrial Metabolism Disease 45 0.741
784
ACT200 Acute Monoblastic Leukemia 40 0.741
785
P ADL017 Adult T-Cell Leukemia 54 0.739
786
KDN013 Kidney Hypertrophy 33 0.735
787
c MCR112 Microvascular Complications of Diabetes 2 42 0.730
788
P CRN024 Corneal Disease 43 0.730
789
AND014 Androgenic Alopecia 46 0.730
790
LTN004 Late-Onset Retinal Degeneration 60 0.730
791
c LKM070 Leukemia, Acute Monocytic 56 0.730
792
P MVM001 Movement Disease 61 0.730
793
P ATR010 Atrial Heart Septal Defect 58 0.730
794
ACR007 Acromegaly 70 0.730
795
ORC001 Orchitis 44 0.730
796
CRB090 Cerebral Hypoxia 42 0.730
797
ACT162 Acute Sensory Ataxic Neuropathy 24 0.730
798
P PRC019 Precocious Puberty 49 0.730
799
P GRV001 Graves' Disease 54 0.719
800
GST033 Gestational Diabetes 61 0.719
801
YLL002 Yellow Fever 61 0.719
802
c HNT004 Huntington Disease-Like 2 51 0.718
803
CRY014 Cryptococcal Meningitis 48 0.718
804
c BRS110 Breast-Ovarian Cancer, Familial 1 58 0.718
805
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.718
806
LKS001 Leukostasis 40 0.718
807
P OST001 Osteopetrosis 70 0.718
808
P VNT002 Ventricular Septal Defect 58 0.718
809
c PNC106 Pancreatic Agenesis 1 51 0.718
810
MDS022 Mediastinitis 47 0.718
811
CRN020 Coronary Restenosis 39 0.718
812
c NLD014 Nail Disorder, Nonsyndromic Congenital, 4 39 0.715
813
P THR117 Three M Syndrome 1 64 0.715
814
FCL009 Focal Dermal Hypoplasia 64 0.715
815
c BRC078 Brachydactyly, Type A1 53 0.715
816
ADP007 Adie Pupil 40 0.715
817
DPN005 Du Pan Syndrome 47 0.715
818
LYM004 Lymphoid Interstitial Pneumonia 49 0.715
819
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.715
820
SYN086 Synostoses, Tarsal, Carpal, and Digital 37 0.715
821
TBH001 Tibia, Hypoplasia or Aplasia of, with Polydactyly 46 0.715
822
P TTR031 Tetraamelia Syndrome 35 0.715
823
P BND014 Bone Development Disease 33 0.715
824
AND001 Anodontia 42 0.715
825
HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 35 0.715
826
P PHC014 Phocomelia 23 0.715
827
AML065 Amelia 29 0.715
828
HNM002 Hinman Syndrome 26 0.715
829
RCK004 Rickets 65 0.712
830
OPT003 Opiate Dependence 49 0.712
831
PRP030 Purpura 54 0.712
832
CHR178 Chromosomal Triplication 34 0.712
833
c FNC043 Fanconi Anemia, Complementation Group E 62 0.710
834
PLY105 Polycystic Ovary Syndrome 1 39 0.710
835
AND005 Androgen Insensitivity Syndrome, Mild 21 0.710
836
P ZNC008 Zinc Finger Protein 1 22 0.705
837
TNG007 Tongue Carcinoma 55 0.705
838
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 65 0.705
839
SPN019 Spondylolisthesis 52 0.705
840
c SPS214 Spastic Ataxia 4 23 0.705
841
c SPS208 Spastic Ataxia 4, Autosomal Recessive 27 0.705
842
CND002 Conduct Disorder 50 0.705
843
TTR011 Tetraploidy 43 0.705
844
P SCK005 Sickle Cell Disease 56 0.705
845
CRD137 Cardiogenic Shock 56 0.705
846
LNG031 Lung Benign Neoplasm 51 0.702
847
c HPT015 Hepatitis D 49 0.697
848
c CHR684 Chronic Kidney Disease 74 0.697
849
P ALP061 Alopecia, Androgenetic, 1 49 0.691
850
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.691
851
DYS015 Dysentery 50 0.691
852
P DMY001 Demyelinating Polyneuropathy 41 0.691
853
P HYP040 Hypospadias 51 0.691
854
P HYP024 Hypoparathyroidism 55 0.691
855
MST020 Mast Cell Activation Syndrome 27 0.691
856
SNL007 Senile Cataract 40 0.691
857
MSC007 Muscle Hypertrophy 64 0.689
858
P PLY018 Polycythemia 56 0.689
859
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.689
860
P SPN301 Spinocerebellar Ataxia 2 59 0.682
861
INC002 Inclusion Body Myositis 57 0.682
862
ART016 Aortic Aneurysm 69 0.682
863
PLY100 Polyploidy 36 0.682
864
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.679
865
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.679
866
END062 Endometrial Hyperplasia 48 0.676
867
FCS014 Fucosidase Regulator 15 0.676
868
MYL020 Myelomeningocele 51 0.676
869
P GNG009 Gangliosidosis 44 0.676
870
AMB001 Amebiasis 56 0.676
871
SPP011 Suppression of Tumorigenicity 12 61 0.674
872
CHL028 Childhood Type Dermatomyositis 58 0.668
873
RSP021 Respiratory Allergy 41 0.665
874
BLR008 Bilirubin Metabolic Disorder 57 0.665
875
CMP087 Complement Component 7 Deficiency 37 0.659
876
c HRD202 Hereditary Lymphedema I 55 0.659
877
PRC002 Paracoccidioidomycosis 53 0.659
878
MYT011 Myotonia 38 0.659
879
PRN019 Perinatal Necrotizing Enterocolitis 60 0.659
880
OTT002 Otitis Media 71 0.657
881
P CTN015 Cutaneous T Cell Lymphoma 48 0.657
882
PNG002 Pain Agnosia 51 0.657
883
HRY003 Hairy Cell Leukemia 61 0.657
884
P HMR003 Hemorrhagic Disease 59 0.657
885
P HYP265 Hypotonia 42 0.654
886
SKN013 Skin Benign Neoplasm 49 0.650
887
P EPN001 Ependymoblastoma 44 0.650
888
P NRV007 Nervous System Disease 66 0.650
889
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.650
890
PLY001 Polycythemia Vera 69 0.648
891
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.648
892
P TBR001 Tuberous Sclerosis 69 0.648
893
FBR047 Fibromyalgia 58 0.648
894
HND002 Hand, Foot and Mouth Disease 50 0.648
895
P CRV031 Cervical Adenocarcinoma 48 0.648
896
P HYP076 Hyperthyroidism 53 0.648
897
P LCT002 Lactose Intolerance 52 0.641
898
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.641
899
P HRS035 Hirschsprung Disease 1 66 0.641
900
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 35 0.641
901
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.641
902
VLV011 Vulvovaginal Candidiasis 49 0.641
903
KRT009 Keratosis 52 0.641
904
HST011 Histoplasmosis 54 0.641
905
c GM1007 Gm1 Gangliosidosis 65 0.641
906
DRM011 Dermatophytosis 52 0.641
907
c ACT135 Acute Graft Versus Host Disease 51 0.641
908
INT358 Intestinal Polyposis Syndrome 25 0.641
909
SLD003 Sialadenitis 47 0.639
910
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.639
911
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.639
912
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.639
913
LMY014 Leiomyoma, Uterine 55 0.639
914
TMP009 Temperature-Sensitive Lethal Mutation 9 0.639
915
ANK001 Ankylosis 51 0.639
916
CRB037 Cerebral Palsy 67 0.639
917
SNS003 Sensory Peripheral Neuropathy 51 0.639
918
GTR002 Goiter 52 0.639
919
KRT002 Keratomalacia 54 0.633
920
ADR016 Adrenal Cortical Carcinoma 61 0.630
921
c CHR711 Chronic Asthma 41 0.630
922
BLM001 Bloom Syndrome 65 0.630
923
SPN051 Spondylitis 51 0.630
924
INF009 Inflammatory Spondylopathy 30 0.630
925
ETN001 Eating Disorder 59 0.630
926
c ATM101 Autoimmune Gastritis 40 0.621
927
P SML001 Small Cell Carcinoma 52 0.621
928
P SNS001 Sensorineural Hearing Loss 59 0.621
929
DSS009 Disseminated Intravascular Coagulation 56 0.621
930
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.621
931
CRB086 Cerebral Aneurysms 40 0.621
932
SPT004 Septic Arthritis 58 0.621
933
PLY012 Polyhydramnios 46 0.621
934
CCN001 Cocaine Dependence 48 0.621
935
PRS119 Persistent Genital Arousal Disorder 18 0.621
936
HMF008 Hemifacial Atrophy, Progressive 38 0.618
937
DYS018 Dysostosis 43 0.618
938
FCL003 Facial Hemiatrophy 29 0.618
939
TNC003 Tinea Corporis 39 0.618
940
PNN001 Panniculitis 52 0.618
941
P HYP087 Hypotrichosis 41 0.618
942
c AMY009 Amyloidosis Aa 47 0.618
943
c DWL002 Dowling-Degos Disease 1 58 0.611
944
c HNT011 Huntington Disease-Like 3 33 0.611
945
P ASP006 Aspergillosis 71 0.611
946
c SCH079 Schizophrenia 1 44 0.611
947
PRP016 Paraplegia 52 0.611
948
P MYC033 Myoclonus 46 0.611
949
RFR003 Refractive Error 41 0.611
950
P CNR004 Cone-Rod Dystrophy 2 75 0.609
951
INF158 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations 30 0.600
952
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.600
953
VLV047 Volvulus of Midgut 55 0.600
954
ALT002 Aleutian Mink Disease 27 0.600
955
P PRL003 Proliferative Glomerulonephritis 43 0.600
956