Search results for B2

2217 hits were found for B2

# Family MCID Name MIFTS Score
1
c BRC052 Brachydactyly, Type B2 40 40.800
2
c MSC044 Muscular Dystrophy-Dystroglycanopathy , Type B, 2 31 16.799
3
RBF001 Riboflavin Deficiency 49 13.276
4
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 40 13.005
5
CRT005 Cortical Thymoma 22 9.458
6
ISC004 Ischemia 61 3.925
7
P THY023 Thymoma 64 3.731
8
c THY107 Thymoma, Familial 42 3.725
9
c MGR028 Migraine with or Without Aura 1 64 3.483
10
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.380
11
c ACT068 Acute Cystitis 61 3.348
12
c PRC016 Pre-Eclampsia 64 3.347
13
c HYP595 Hypertension, Essential 84 3.312
14
P ANG015 Angioedema 56 3.237
15
P BRS047 Breast Cancer 97 3.212
16
CRB039 Cerebrovascular Disease 65 3.164
17
CRH001 Crohn's Disease 80 3.120
18
c MCR133 Microvascular Complications of Diabetes 4 41 3.008
19
c MCR113 Microvascular Complications of Diabetes 3 52 3.008
20
c MCR130 Microvascular Complications of Diabetes 6 41 3.008
21
c MCR120 Microvascular Complications of Diabetes 7 47 3.008
22
P URN019 Urinary Tract Infection 49 2.978
23
P ADN016 Adenocarcinoma 63 2.760
24
BRN004 Brain Edema 54 2.738
25
c HPT016 Hepatitis B 62 2.729
26
PRT037 Pertussis 49 2.703
27
P KDN018 Kidney Disease 72 2.633
28
LPP008 Lipoprotein Quantitative Trait Locus 65 2.594
29
c CHR684 Chronic Kidney Disease 74 2.581
30
P PRS040 Prostate Cancer 95 2.532
31
KRT002 Keratomalacia 54 2.510
32
P AST005 Asthma 76 2.505
33
ART140 Arteries, Anomalies of 52 2.502
34
P MYC008 Myocarditis 59 2.494
35
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.465
36
48X005 48,xyyy 39 2.443
37
HLX001 Helix Syndrome 47 2.387
38
P INF032 Infertility 60 2.358
39
P CLR023 Colorectal Cancer 100 2.313
40
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.313
41
c HYP836 Hypercholesterolemia, Familial, 1 73 2.291
42
P LVR013 Liver Disease 68 2.267
43
CRV035 Cervical Cancer 72 2.262
44
P BLD134 Bladder Cancer 79 2.234
45
ANG054 Angina Pectoris 65 2.182
46
P ECL001 Eclampsia 52 2.178
47
P INF037 Inflammatory Bowel Disease 53 2.176
48
PST011 Pustulosis of Palm and Sole 52 2.168
49
P PSR002 Psoriasis 63 2.168
50
47X002 47,xyy 48 2.164
51
OST012 Osteoarthritis 77 2.159
52
AZS001 Azoospermia 45 2.145
53
TRM010 Traumatic Brain Injury 50 2.138
54
c HRD002 Hereditary Angioedema 61 2.123
55
P HPT023 Hepatocellular Carcinoma 95 2.108
56
P HRT032 Heart Disease 84 2.102
57
P PLM037 Pulmonary Hypertension 69 2.100
58
GLM045 Glioma 62 2.098
59
P RHN004 Rhinitis 57 2.089
60
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.068
61
ATH013 Atherosclerosis Susceptibility 63 2.067
62
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.054
63
P CRN300 Coronary Heart Disease 1 73 2.048
64
END086 End Stage Renal Disease 54 2.041
65
P ANR048 Aniridia 1 66 2.037
66
GLL048 Glial Tumor 52 2.019
67
FTT001 Fatty Liver Disease 61 1.994
68
STR067 Stroke, Ischemic 79 1.974
69
P RCT021 Rectum Cancer 54 1.972
70
INT007 Intermediate Coronary Syndrome 53 1.952
71
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.945
72
CRB004 Cerebral Artery Occlusion 46 1.926
73
TXC005 Toxic Shock Syndrome 62 1.903
74
c ATR087 Atrial Standstill 1 74 1.903
75
HYP066 Hyperglycemia 60 1.900
76
PRT251 Proteinuria, Chronic Benign 58 1.886
77
DWN001 Down Syndrome 70 1.880
78
P MLN007 Male Infertility 56 1.865
79
P NRB001 Neuroblastoma 66 1.863
80
P HPT021 Hepatitis 68 1.861
81
P NRP001 Neuropathy 59 1.858
82
SPN186 Spinal Cord Injury 61 1.837
83
BCT022 Bacterial Infectious Disease 56 1.831
84
ATM095 Autoimmune Disease 61 1.831
85
BRN071 Brain Injury 50 1.829
86
ALL029 Allergic Disease 61 1.816
87
P DBT009 Diabetes Mellitus 67 1.809
88
P MYC007 Myocardial Infarction 69 1.797
89
P THL005 Thalassemia 56 1.767
90
P LNG032 Lung Cancer 98 1.763
91
END057 Endometrial Cancer 71 1.763
92
P VSC007 Vascular Disease 62 1.762
93
BNR002 Bone Resorption Disease 47 1.758
94
MTH009 Mouth Disease 57 1.758
95
P FBR017 Fibrosarcoma 55 1.739
96
P LPS004 Lupus Erythematosus 61 1.726
97
P THR014 Thrombocytopenia 66 1.722
98
P MYS003 Myasthenia Gravis 68 1.721
99
ALL003 Allergic Rhinitis 66 1.704
100
CLR109 Colorectal Adenocarcinoma 50 1.693
101
LNG099 Lung Disease 62 1.693
102
EMB004 Embryonal Carcinoma 55 1.688
103
PRS047 Prostatitis 58 1.682
104
P PRK057 Parkinson Disease, Late-Onset 79 1.681
105
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.676
106
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.673
107
CLT003 Colitis 63 1.673
108
HYP266 Hypoxia 56 1.672
109
CNG034 Congestive Heart Failure 69 1.660
110
c BLD156 Bleeding Disorder, Platelet-Type, 14 33 1.648
111
NTR005 Nutritional Deficiency Disease 60 1.640
112
P GST053 Gastric Cancer 82 1.629
113
c ACT075 Acute Myocardial Infarction 55 1.624
114
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.615
115
P CRD246 Cardiovascular System Disease 55 1.606
116
P MNN013 Meningitis 65 1.600
117
C1N001 C1 Inhibitor Deficiency 43 1.596
118
NRL016 Neural Tube Defects 81 1.591
119
ADN018 Adenoma 58 1.590
120
ULC004 Ulcerative Colitis 74 1.590
121
URT010 Ureteral Obstruction 45 1.585
122
NNT021 Neonatal Meningitis 22 1.585
123
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.585
124
CLN015 Colon Adenocarcinoma 64 1.584
125
HMC014 Homocysteinemia 52 1.578
126
c TYP009 Type 2 Diabetes Mellitus 92 1.578
127
P SLP006 Sleep Apnea 69 1.577
128
c PRM038 Primary Agammaglobulinemia 47 1.569
129
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.568
130
AGN016 Aging 54 1.564
131
c CTR132 Cataract 3, Multiple Types 41 1.563
132
P FNG006 Feingold Syndrome 1 61 1.556
133
c HPT001 Hepatitis C 61 1.541
134
P DRR001 Diarrhea 55 1.538
135
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.533
136
c SML038 Small Cell Cancer of the Lung 69 1.532
137
RNL077 Renal Fibrosis 46 1.528
138
c SPR162 Spermatogenic Failure 50 42 1.527
139
P HDC001 Headache 56 1.516
140
P CTR002 Cataract 59 1.516
141
ESP021 Esophageal Cancer 84 1.513
142
KRT019 Keratitis, Hereditary 66 1.507
143
CYT002 Cytokine Deficiency 43 1.503
144
STT002 Status Asthmaticus 49 1.502
145
DBT010 Diabetic Neuropathy 54 1.499
146
P MTR012 Mitral Valve Disease 57 1.495
147
IRN002 Iron Metabolism Disease 56 1.495
148
P ENC004 Encephalitis 61 1.492
149
P CYS018 Cystitis 59 1.487
150
P TMP001 Temporal Lobe Epilepsy 49 1.486
151
FDB001 Foodborne Botulism 55 1.474
152
P GLM007 Glomerulonephritis 59 1.461
153
P PYL005 Pyelonephritis 56 1.452
154
ADR040 Adrenal Gland Pheochromocytoma 45 1.447
155
P PHC003 Pheochromocytoma 70 1.447
156
P LCT001 Lactic Acidosis 50 1.441
157
PRT036 Peritonitis 65 1.441
158
P PRD008 Periodontitis 64 1.429
159
SQM006 Squamous Cell Carcinoma 59 1.425
160
SKN016 Skin Disease 62 1.422
161
P ADL010 Adult Respiratory Distress Syndrome 71 1.414
162
DFC004 Deficiency Anemia 74 1.408
163
P CLC063 Celiac Disease 1 66 1.396
164
HND002 Hand, Foot and Mouth Disease 50 1.396
165
P NPH012 Nephrotic Syndrome 62 1.394
166
SVR004 Severe Combined Immunodeficiency 71 1.379
167
P NTR004 Neutropenia 62 1.377
168
GLB002 Glioblastoma 67 1.372
169
P AMY004 Amyloidosis 69 1.371
170
ALL006 Allergic Asthma 56 1.371
171
c SYS001 Systemic Lupus Erythematosus 86 1.370
172
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.370
173
P HYP750 Hypertriglyceridemia, Familial 62 1.370
174
PLM010 Pulmonary Edema 54 1.366
175
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.361
176
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.361
177
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.361
178
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.361
179
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.361
180
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.361
181
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.361
182
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.361
183
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.361
184
P INS002 in Situ Carcinoma 53 1.357
185
MTB004 Metabolic Acidosis 48 1.353
186
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.352
187
P ANT006 Antiphospholipid Syndrome 55 1.346
188
MNN009 Meningoencephalitis 48 1.346
189
PLR008 Pleurisy 49 1.333
190
CHL014 Cholera 62 1.327
191
ART016 Aortic Aneurysm 69 1.327
192
P PNC044 Pancreatitis 61 1.314
193
P ART021 Arteriosclerosis 53 1.313
194
HGH043 High Grade Glioma 46 1.306
195
ASP030 Aspirin Resistance 40 1.305
196
P GST044 Gastritis 55 1.303
197
P RNV001 Renovascular Hypertension 49 1.299
198
ASP003 Aseptic Meningitis 51 1.294
199
P PLY019 Polyneuropathy 53 1.293
200
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.284
201
c LKM005 Leukemia, T-Cell, Chronic 33 1.284
202
P MYC084 Mycobacterium Tuberculosis 1 68 1.283
203
HDN002 Head Injury 44 1.282
204
ALC007 Alcohol Dependence 65 1.270
205
CLR108 Colorectal Adenoma 63 1.269
206
OST017 Osteomyelitis 63 1.268
207
P MTC069 Mitochondrial Disorders 57 1.258
208
OST159 Osteogenic Sarcoma 66 1.256
209
RCK004 Rickets 65 1.254
210
P RTN024 Retinoblastoma 72 1.250
211
P KLZ004 Kala-Azar 1 41 1.250
212
c DLT002 Dilated Cardiomyopathy 79 1.250
213
LSH001 Leishmaniasis 63 1.250
214
PHR003 Pharyngitis 57 1.244
215
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.239
216
LVR012 Liver Cirrhosis 62 1.237
217
DSS032 Disease by Infectious Agent 55 1.231
218
P END044 Endometriosis 62 1.231
219
c ACT071 Acute Kidney Failure 60 1.231
220
c BTT014 Beta-Thalassemia 72 1.219
221
OCL069 Ocular Motor Apraxia 57 1.217
222
DCT002 Ductal Carcinoma in Situ 58 1.217
223
P HRP006 Herpes Simplex 65 1.217
224
HLC007 Helicobacter Pylori Infection 67 1.216
225
c MCR115 Microvascular Complications of Diabetes 5 65 1.203
226
P ALZ034 Alzheimer Disease 87 1.197
227
LMB062 Limb Ischemia 55 1.190
228
SRC014 Sarcoma 64 1.190
229
TRN018 Transitional Cell Carcinoma 56 1.190
230
SPN035 Spindle Cell Sarcoma 51 1.190
231
MSL001 Measles 61 1.190
232
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.186
233
c PCH010 Pachyonychia Congenita 3 43 1.183
234
MCR004 Macroglobulinemia 48 1.183
235
c FML021 Familial Hypercholesterolemia 71 1.182
236
P LYM118 Lymphoma 69 1.176
237
P LKM002 Leukemia 66 1.176
238
BRN009 Burning Mouth Syndrome 51 1.174
239
APN008 Apnea, Obstructive Sleep 66 1.172
240
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.167
241
c ACT027 Acute Pancreatitis 60 1.165
242
P LKM062 Leukemia, Acute Lymphoblastic 69 1.160
243
THR024 Thrombosis 56 1.154
244
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.145
245
THY089 Thymic Epithelial Neoplasm 27 1.144
246
P MSC005 Muscular Dystrophy 66 1.142
247
THY042 Thymic Epithelial Tumor 26 1.138
248
MCS002 Mucositis 55 1.137
249
P EXN002 Exanthem 58 1.137
250
c HPT073 Hepatitis C Virus 71 1.137
251
P INF038 Influenza 68 1.136
252
P PRK039 Parkinsonism 55 1.135
253
P RHB003 Rhabdomyosarcoma 66 1.128
254
BRS099 Breast Ductal Carcinoma 61 1.121
255
GST040 Gastric Adenocarcinoma 66 1.121
256
HMN044 Human Immunodeficiency Virus Type 1 76 1.118
257
LPD008 Lipid Metabolism Disorder 61 1.118
258
CHL068 Cholestasis 61 1.113
259
PLM001 Pulmonary Tuberculosis 69 1.113
260
CRN027 Corneal Neovascularization 47 1.113
261
ORL015 Oral Squamous Cell Carcinoma 43 1.112
262
P MYP006 Myopia 55 1.112
263
P PNC035 Pancreatic Cancer 86 1.103
264
BLD131 Bladder Urothelial Carcinoma 59 1.094
265
P ALC033 Alcohol Use Disorder 67 1.090
266
HPT014 Hepatorenal Syndrome 49 1.090
267
P LKM071 Leukemia, Chronic Lymphocytic 74 1.086
268
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.085
269
IMP005 Impotence 52 1.085
270
PRP030 Purpura 54 1.085
271
P MYP004 Myopathy 67 1.085
272
RTN020 Retinal Vascular Disease 45 1.080
273
P MYL006 Myeloid Leukemia 60 1.080
274
MYL069 Myeloma, Multiple 77 1.079
275
MLR004 Malaria 78 1.078
276
PLC008 Placenta Disease 49 1.078
277
STM007 Stomatitis 52 1.066
278
SBC016 Subacute Delirium 42 1.065
279
PRP027 Peripheral Vascular Disease 71 1.059
280
CTN007 Cutaneous Leishmaniasis 61 1.054
281
INS024 Insulin-Like Growth Factor I 77 1.052
282
P RSP003 Respiratory Failure 74 1.052
283
HMG005 Hemoglobinopathy 55 1.046
284
CMP040 Complement Component 4, Partial Deficiency of 34 1.038
285
KPS004 Kaposi Sarcoma 76 1.038
286
P CRN026 Corneal Edema 42 1.038
287
P CNJ013 Conjunctivitis 66 1.038
288
ACT003 Acute Kidney Tubular Necrosis 46 1.024
289
GT001 Gout 63 1.024
290
DRM006 Dermatitis 62 1.024
291
CRN017 Coronary Thrombosis 46 1.023
292
P SRC025 Sarcoidosis 1 70 1.022
293
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.015
294
P BND020 Bone Disease 60 1.015
295
PPT005 Peptic Ulcer Disease 58 1.015
296
PRT049 Partial Deletion of Y 33 1.015
297
BRN024 Bronchitis 67 1.013
298
ALC006 Alcoholic Hepatitis 61 1.012
299
THY022 Thymic Carcinoma 56 1.011
300
SYN007 Synovitis 54 1.007
301
PLC002 Plica Syndrome 35 1.007
302
TRT001 Teratocarcinoma 41 1.007
303
ALL014 Allergic Encephalomyelitis 34 1.007
304
INT078 Intracranial Thrombosis 50 1.000
305
P PLM036 Pulmonary Fibrosis 65 0.999
306
PST092 Posttransplant Acute Limbic Encephalitis 29 0.999
307
ANT039 Antisynthetase Syndrome 55 0.998
308
P CRP001 Carpal Tunnel Syndrome 66 0.987
309
DBT004 Diabetic Polyneuropathy 50 0.987
310
P SZR006 Seizure Disorder 69 0.983
311
CRD137 Cardiogenic Shock 56 0.983
312
ACT098 Acute Erythroid Leukemia 55 0.974
313
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.974
314
P BRC006 Brachydactyly 52 0.958
315
P PRP019 Peripheral Nervous System Disease 57 0.957
316
ACT119 Acute Promyelocytic Leukemia 62 0.957
317
P NSP012 Nasopharyngeal Carcinoma 60 0.957
318
PYR009 Pyridoxine Deficiency Anemia 35 0.957
319
ARG004 Argyria 26 0.957
320
ADL002 Adult Syndrome 69 0.954
321
c PNS012 Paine Syndrome 60 0.954
322
RHB024 Rhabdomyosarcoma 2 65 0.954
323
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.954
324
c PRS130 Prostate Cancer, Hereditary, 8 32 0.954
325
c PRS136 Prostate Cancer, Hereditary, 6 33 0.954
326
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.954
327
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.954
328
RFR003 Refractive Error 41 0.954
329
c BLD123 Bleeding Disorder, Platelet-Type, 13 22 0.951
330
PRC013 Pericarditis 53 0.948
331
P ALP008 Alopecia 53 0.948
332
P CHR345 Chronic Pain 50 0.944
333
P BCL017 B-Cell Lymphoma 57 0.939
334
SFT003 Soft Tissue Sarcoma 57 0.938
335
P PLY018 Polycythemia 56 0.938
336
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.933
337
c TYP008 Type 1 Diabetes Mellitus 77 0.933
338
P SPP010 Suppressor of Tumorigenicity 3 51 0.928
339
P ESS003 Essential Thrombocythemia 68 0.928
340
P DDN001 Duodenal Ulcer 53 0.928
341
THR004 Thrombocytosis 52 0.928
342
P BNG032 Benign Mesothelioma 53 0.928
343
SPP011 Suppression of Tumorigenicity 12 61 0.928
344
P HYP086 Hypothyroidism 69 0.926
345
P ADL017 Adult T-Cell Leukemia 54 0.918
346
ENT011 Enterocolitis 55 0.918
347
P ATR011 Atrial Fibrillation 66 0.908
348
P LSS002 Lissencephaly 53 0.908
349
FBR047 Fibromyalgia 58 0.908
350
c LKM063 Leukemia, Chronic Myeloid 71 0.907
351
MST005 Mastitis 52 0.907
352
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.897
353
DSS009 Disseminated Intravascular Coagulation 56 0.897
354
P MLT074 Multiple Endocrine Neoplasia 58 0.897
355
P PRX021 Proximal Symphalangism 50 0.892
356
ANK001 Ankylosis 51 0.892
357
c ALP101 Alpha-Thalassemia 62 0.887
358
STT001 Status Epilepticus 58 0.886
359
BRN028 Brain Cancer 73 0.886
360
GNG013 Gingivitis 59 0.886
361
P VNW001 Von Willebrand's Disease 64 0.886
362
GST045 Gastroenteritis 58 0.886
363
P EST010 Esterase B 13 0.880
364
BRN002 Bronchiolitis 57 0.880
365
P DRM053 Dermatitis, Atopic 65 0.874
366
P NRF002 Neurofibromatosis 60 0.874
367
P FML187 Familial Hypertension 34 0.874
368
TRS002 Tarsal-Carpal Coalition Syndrome 42 0.871
369
SYN005 Synostosis 43 0.871
370
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.866
371
P MTC133 Mitochondrial Myopathy 51 0.862
372
c ACT076 Acute Myocarditis 47 0.862
373
P RNL007 Renal Tubular Acidosis 52 0.858
374
c BRN108 Branchiootic Syndrome 1 63 0.849
375
RNL025 Renal Hypoplasia 46 0.849
376
P HML001 Hemolytic-Uremic Syndrome 52 0.849
377
PLN006 Poland Syndrome 45 0.846
378
P MLT072 Multiple Synostoses Syndrome 44 0.846
379
STP011 Stapes Ankylosis with Broad Thumbs and Toes 28 0.846
380
BRK010 Burkitt Lymphoma 66 0.843
381
c MST023 Mesothelioma, Malignant 56 0.836
382
P SKN015 Skin Carcinoma 71 0.836
383
P MLN008 Melanoma 75 0.828
384
MTR002 Mitral Valve Insufficiency 51 0.828
385
IMM165 Immunoglobulin Switch Sequences 14 0.821
386
PRP080 Peripheral Artery Disease 54 0.820
387
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.820
388
P MMB011 Membranous Nephropathy 50 0.820
389
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.820
390
P INT068 Intestinal Disease 53 0.820
391
GTR002 Goiter 52 0.820
392
GLM044 Glomerular Disease 34 0.820
393
c BRC051 Brachydactyly, Type B1 50 0.813
394
RCT020 Rectum Adenocarcinoma 48 0.812
395
P DST107 Distal Renal Tubular Acidosis 48 0.812
396
NRR001 Neuroretinitis 42 0.811
397
RTN023 Retinitis 45 0.811
398
IRN001 Iron Deficiency Anemia 58 0.806
399
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.804
400
P MYS005 Myositis 56 0.804
401
P OST002 Osteoporosis 77 0.804
402
c SVR005 Severe Pre-Eclampsia 50 0.804
403
CLN045 Colonic Benign Neoplasm 48 0.789
404
P OST001 Osteopetrosis 70 0.789
405
ECH003 Echinococcosis 52 0.789
406
P ZLL001 Zellweger Syndrome 65 0.789
407
VRC005 Varicose Veins 59 0.786
408
ART074 Aortic Dissection 53 0.786
409
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.786
410
PLM031 Poliomyelitis 62 0.786
411
P PTT006 Pituitary Adenoma 55 0.786
412
P GLL018 Gallbladder Cancer 53 0.786
413
HYP056 Hypoglycemia 65 0.786
414
P MLT020 Multiple Sclerosis 79 0.782
415
CYS008 Cystic Echinococcosis 57 0.770
416
P HMP007 Hemophilia 52 0.770
417
P RTN016 Retinal Degeneration 52 0.770
418
c LKM061 Leukemia, Acute Myeloid 83 0.768
419
c JVN010 Juvenile Rheumatoid Arthritis 66 0.768
420
c BSL007 Basal Cell Carcinoma 68 0.759
421
P PLY011 Polycystic Ovary Syndrome 57 0.759
422
ANR040 Aneurysm 60 0.759
423
IRR002 Irritable Bowel Syndrome 65 0.759
424
P SCH015 Schizophrenia 74 0.757
425
NNL006 Non-Alcoholic Steatohepatitis 54 0.752
426
MCN001 Mucinous Adenocarcinoma 49 0.752
427
APP009 Appendix Adenocarcinoma 47 0.752
428
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.752
429
c TBR025 Tuberous Sclerosis 1 84 0.749
430
P TBR001 Tuberous Sclerosis 69 0.749
431
c ACT249 Acute Asthma 40 0.749
432
URM002 Uremia 47 0.749
433
TYP007 Typhoid Fever 63 0.749
434
P HYD006 Hydrocephalus 63 0.749
435
INS001 Insulinoma 59 0.749
436
P SLP005 Sleep Disorder 62 0.749
437
P KRT007 Keratoconus 50 0.740
438
PNC129 Pancreatic Adenocarcinoma 65 0.739
439
c ACQ012 Acquired Angioedema 37 0.739
440
MTC100 Metacarpal 4-5 Fusion 31 0.734
441
SGR001 Sugarman Brachydactyly 32 0.734
442
c BRC078 Brachydactyly, Type A1 53 0.734
443
c BRC079 Brachydactyly, Type A2 50 0.734
444
c BRC099 Brachydactyly, Type A4 30 0.734
445
ADP007 Adie Pupil 40 0.734
446
DPN005 Du Pan Syndrome 47 0.734
447
LCR014 Lacrimoauriculodentodigital Syndrome 58 0.734
448
OSS012 Osseous Heteroplasia, Progressive 61 0.734
449
c BRC075 Brachydactyly, Type A1, C 33 0.734
450
c MCR109 Microphthalmia, Isolated 4 37 0.734
451
SYN086 Synostoses, Tarsal, Carpal, and Digital 37 0.734
452
SYM024 Symphalangism, Distal 21 0.734
453
P SYN060 Syndactyly, Type Iii 40 0.734
454
ICH054 Ichthyosis, X-Linked 51 0.734
455
c BRC080 Brachydactyly, Type A1, B 37 0.734
456
HNM002 Hinman Syndrome 26 0.734
457
PLY001 Polycythemia Vera 69 0.729
458
P OPN001 Open-Angle Glaucoma 55 0.729
459
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.729
460
c GLC092 Glaucoma, Primary Open Angle 61 0.729
461
c THR092 Thrombophilia Due to Thrombin Defect 74 0.729
462
CHG001 Chagas Disease 65 0.729
463
AVN001 Avian Influenza 61 0.729
464
P HYP098 Hypereosinophilic Syndrome 66 0.729
465
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.724
466
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.724
467
MTC004 Mitochondrial Encephalomyopathy 43 0.724
468
PYR016 Pyridoxine Deficiency 29 0.724
469
DFF005 Diffuse Large B-Cell Lymphoma 55 0.718
470
P SCL018 Scoliosis 57 0.718
471
P CRC039 Coarctation of Aorta 46 0.718
472
HMP001 Hemopericardium 47 0.718
473
P PRC012 Pericardial Effusion 50 0.718
474
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.718
475
P MSC003 Muscular Atrophy 52 0.718
476
PDT035 Pediatric Systemic Lupus Erythematosus 46 0.718
477
CRH005 Crohn's Colitis 53 0.711
478
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.707
479
CRN019 Coronary Artery Vasospasm 47 0.707
480
P CND004 Candidiasis 57 0.707
481
P HML002 Hemolytic Anemia 62 0.707
482
SCH014 Schistosomiasis 56 0.707
483
GST023 Gastric Ulcer 52 0.707
484
P PTN014 Patent Ductus Arteriosus 1 59 0.707
485
PLM033 Pulmonary Embolism 58 0.707
486
CNS004 Constipation 56 0.701
488
PNG002 Pain Agnosia 51 0.695
489
BNB002 Bainbridge-Ropers Syndrome 45 0.695
490
HYD002 Hydronephrosis 58 0.695
491
c DPH024 Diaphragmatic Hernia, Congenital 64 0.695
492
NWC001 Newcastle Disease 48 0.695
493
P BRS044 Breast Adenocarcinoma 58 0.695
494
HRT012 Heart Valve Disease 53 0.695
495
PRN019 Perinatal Necrotizing Enterocolitis 60 0.695
496
CYS014 Cystadenocarcinoma 51 0.695
497
c CTR130 Cataract 9, Multiple Types 39 0.691
498
LST001 Listeriosis 59 0.691
499
CTR014 Cataract Microcornea Syndrome 35 0.691
500
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.691
501
SLP001 Sleeping Sickness 56 0.683
502
IFP003 Ifap Syndrome 2 42 0.683
503
P ART005 Arteriovenous Malformation 65 0.683
504
P GLM040 Glioma Susceptibility 1 70 0.683
505
P OPT006 Optic Nerve Disease 57 0.683
506
ASP038 Aspirin-Induced Respiratory Disease 16 0.683
507
BTT017 Beta-Thalassemia Major 53 0.683
508
P ESP024 Esophagitis 60 0.683
509
MCL006 Macular Retinal Edema 56 0.683
510
TRN015 Transient Cerebral Ischemia 62 0.683
512
P ATR005 Atrophic Gastritis 50 0.683
513
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.683
514
THY025 Thymus Cancer 56 0.681
515
c HPT003 Hepatitis a 63 0.680
516
P TRN020 Turner Syndrome 67 0.680
517
ART141 Arteriovenous Malformations of the Brain 58 0.670
518
MSC007 Muscle Hypertrophy 64 0.670
519
END062 Endometrial Hyperplasia 48 0.670
520
P MMP001 Mumps 56 0.670
521
GLL029 Gallbladder Adenoma 30 0.670
522
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.670
523
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.670
524
MLG169 Malignant Astrocytoma 57 0.670
525
P PRN023 Prion Disease 60 0.670
526
P HYP069 Hyperparathyroidism 62 0.670
527
MSC157 Muscular Dystrophy, Duchenne Type 79 0.670
528
P TRM003 Tremor 50 0.670
529
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.670
530
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.670
531
c ACT134 Acute Liver Failure 57 0.670
532
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.669
533
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.669
534
PST028 Post-Traumatic Stress Disorder 59 0.657
536
INT395 Intracranial Meningioma 48 0.656
537
TRY001 Trypanosomiasis 50 0.656
538
END041 Endometrial Adenocarcinoma 63 0.656
539
DNT012 Dental Caries 53 0.656
540
CRB037 Cerebral Palsy 67 0.656
541
HRT011 Heart Septal Defect 49 0.656
542
P KRT005 Keratoacanthoma 47 0.656
543
P EPD016 Epidermolysis Bullosa 53 0.656
544
PHN003 Phenylketonuria 76 0.656
545
MNN043 Meningioma, Familial 79 0.656
546
SCR001 Secretory Meningioma 40 0.656
547
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.656
548
THR035 Thrombasthenia 48 0.656
549
EXN003 Exencephaly 30 0.656
550
PRQ002 Paraquat Poisoning 28 0.656
551
PRS063 Paresthesia 39 0.645
552
ADN027 Adenomyosis 59 0.642
553
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.642
554
BRR014 Barrett Esophagus 66 0.642
555
TNG007 Tongue Carcinoma 55 0.642
556
CMM005 Common Cold 55 0.642
557
PLC001 Placenta Accreta 44 0.642
558
URN010 Urinary Tract Obstruction 55 0.642
559
P HYP040 Hypospadias 51 0.642
560
LPT001 Leptospirosis 66 0.642
561
CHL067 Cholecystitis 59 0.642
562
HYP014 Hyperuricemia 51 0.642
563
P VNT002 Ventricular Septal Defect 58 0.642
564
P RTN022 Retinal Vein Occlusion 54 0.642
565
P PLL002 Pellagra 46 0.642
566
MLG079 Malignant Pleural Mesothelioma 42 0.642
567
GRN017 Granulocytopenia 42 0.642
568
ORL011 Oral Cancer 60 0.642
569
P HMC002 Homocystinuria 52 0.642
570
P OVR082 Overgrowth Syndrome 42 0.642
571
HYP005 Hypokalemia 55 0.632
572
P PLY041 Polymyositis 59 0.627
573
BCL014 B-Cell Growth Factor 32 0.627
574
SPS007 Spastic Cerebral Palsy 46 0.627
575
SRC027 Sarcoma, Synovial 58 0.627
576
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.627
577
MYL031 Myeloproliferative Neoplasm 66 0.627
578
DBT007 Diabetic Cataract 35 0.627
579
HMS001 Hemosiderosis 48 0.627
580
CRT004 Carotid Artery Thrombosis 39 0.627
581
CLL003 Cellulitis 53 0.627
582
CCC002 Coccidiosis 50 0.627
583
BRS051 Breast Disease 58 0.627
584
LYS002 Lysosomal Storage Disease 51 0.627
585
ANX004 Anoxia 40 0.627
586
ADG002 Audiogenic Seizures 25 0.627
587
P RRH023 Rare Hereditary Hemochromatosis 53 0.627
588
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.619
589
P LTR001 Lateral Sclerosis 58 0.619
590
END040 Endogenous Depression 54 0.619
591
DPR016 Depression 65 0.619
592
GST050 Gastrointestinal System Disease 55 0.619
593
CPR004 Coproporphyria, Hereditary 57 0.613
594
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.613
595
NNT012 Neonatal Jaundice 53 0.613
596
RNL078 Renal Dysplasia 46 0.613
597
CHR005 Chorioamnionitis 50 0.610
598
P LYM033 Lymphoproliferative Syndrome 59 0.610
599
P ACN011 Acne 55 0.610
600
c VRL007 Viral Encephalitis 50 0.610
601
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.610
602
PLS007 Plasmodium Falciparum Malaria 52 0.610
603
ASP004 Asphyxia Neonatorum 50 0.610
604
P MST009 Mastocytosis 64 0.610
605
SKN005 Skin Atrophy 41 0.610
606
THL004 Theileriasis 26 0.610
607
VSC003 Visceral Leishmaniasis 54 0.610
608
PTH003 Pathologic Nystagmus 52 0.610
609
P RBL001 Rubella 58 0.610
610
FSC002 Fascioliasis 44 0.610
611
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.610
612
LMN011 Laminopathy 35 0.610
613
PLY100 Polyploidy 36 0.610
614
c VRL010 Viral Hepatitis 52 0.604
615
LMY002 Leiomyoma 51 0.604
616
APH001 Aphthous Stomatitis 57 0.604
617
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.602
618
CHR682 Chronic Bilirubin Encephalopathy 37 0.602
619
c NRF023 Neurofibromatosis, Type Ii 70 0.591
620
RST011 Restrictive Dermopathy, Lethal 51 0.591
621
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 24 0.591
623
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.591
624
TNG009 Tongue Squamous Cell Carcinoma 43 0.591
625
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.591
626
c CRD150 Cardiomyopathy, Familial Hypertrophic, 18 25 0.591
627
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.591
628
RNL051 Renal Cysts and Diabetes Syndrome 57 0.591
629
P BRB001 Beriberi 44 0.591
630
NPH009 Nephrolithiasis 54 0.591
631
P RTN018 Retinal Disease 53 0.591
632
KWS001 Kwashiorkor 44 0.591
633
ALC009 Alcoholic Liver Cirrhosis 54 0.591
634
P HYP061 Hypertrophic Cardiomyopathy 69 0.591
635
DBT008 Diabetic Angiopathy 47 0.591
636
P INT099 Intrahepatic Cholestasis of Pregnancy 61 0.591
637
INT075 Intracranial Hypertension 52 0.591
638
P SBR004 Seborrheic Dermatitis 44 0.591
639
ART008 Arteriosclerosis Obliterans 40 0.591
640
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.591
641
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.591
642
HPR003 Heparin-Induced Thrombocytopenia 47 0.591
643
LRY026 Laryngeal Cleft 28 0.591
644
CVD001 Covid-19 58 0.589
645
P MJR001 Major Depressive Disorder 68 0.589
646
MNT002 Mental Depression 56 0.589
647
PRT038 Protein-Energy Malnutrition 53 0.589
648
P BRN022 Bronchiectasis 59 0.589
649
P PLY014 Polycystic Kidney Disease 71 0.583
650
P RHM011 Rheumatoid Arthritis 81 0.583
651
PMP014 Pemphigoid 49 0.572
652
P MCR129 Microvascular Complications of Diabetes 1 68 0.572
653
INT002 Intermittent Claudication 61 0.572
654
P MTR014 Motor Neuron Disease 65 0.572
655
MTC005 Mitochondrial Metabolism Disease 45 0.572
656
BLL006 Bullous Pemphigoid 61 0.572
657
THL010 Thalassemia Minor 31 0.570
658
CYS005 Cysticercosis 60 0.570
659
P BRN019 Bernard-Soulier Syndrome 61 0.570
660
VLV047 Volvulus of Midgut 55 0.570
661
WTH001 Withdrawal Disorder 47 0.570
662
HND015 Hand Skill, Relative 29 0.570
663
P TMP003 Temporal Arteritis 68 0.570
664
CRC001 Cercarial Dermatitis 28 0.570
665
ATR057 Atrioventricular Block 54 0.570
666
c PST001 Posterior Myocardial Infarction 20 0.570
667
MGS001 Megaesophagus 44 0.570
668
P FCL005 Focal Segmental Glomerulosclerosis 57 0.570
669
P AGG001 Aggressive Periodontitis 55 0.570
670
DPH001 Diphtheria 59 0.570
671
P CHR012 Chronic Granulomatous Disease 69 0.570
672
SYS004 Systemic Mastocytosis 62 0.570
673
BLR008 Bilirubin Metabolic Disorder 57 0.570
674
c SCN007 Secondary Hyperparathyroidism 51 0.570
675
P JNC001 Junctional Epidermolysis Bullosa 53 0.570
676
PRS042 Prostate Disease 42 0.570
677
P MLG074 Malignant Mesenchymoma 40 0.570
678
CRL001 Cerulean Cataract 26 0.570
679
c ATM075 Autoimmune Encephalitis 39 0.570
680
ILS001 Ileus 49 0.570
681
c BCT007 Bacterial Meningitis 55 0.570
682
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.570
683
PCH007 Pouchitis 42 0.570
684
BHR001 Behr Syndrome 50 0.558
685
P PRC031 Preeclampsia/eclampsia 1 43 0.558
686
CLN002 Colon Mucinous Adenocarcinoma 28 0.558
687
BRN038 Bronchial Disease 51 0.558
688
AST006 Astigmatism 46 0.553
689
MMM006 Mammographic Density 39 0.553
690
P CRN028 Corneal Ulcer 47 0.553
691
LGH007 Leigh Syndrome 70 0.545
692
c DFN036 Deafness, X-Linked 2 44 0.545
693
P TMR010 Tumor Predisposition Syndrome 69 0.545
694
MRG003 Marginal Zone B-Cell Lymphoma 52 0.545
695
c DWL002 Dowling-Degos Disease 1 58 0.545
696
P SCL047 Sclerocornea 32 0.545
697
P PRP034 Purpura Fulminans 41 0.545
698
P FLL037 Follicular Lymphoma 73 0.545
699
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.545
700
ANG046 Angioimmunoblastic T-Cell Lymphoma 51 0.545
701
DYS015 Dysentery 50 0.545
702
LKS001 Leukostasis 40 0.545
703
CNT047 Contact Dermatitis 57 0.545
704
ANR004 Anuria 44 0.545
705
P PNC025 Panic Disorder 52 0.545
706
FNG003 Fungal Esophagitis 21 0.545
707
ORL005 Oral Candidiasis 55 0.545
708
DRF001 Dirofilariasis 32 0.545
709
CNS002 Constrictive Pericarditis 39 0.545
710
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.545
711
P END047 Endophthalmitis 53 0.545
712
PRP007 Priapism 46 0.545
713
PRN008 Peroneal Nerve Paralysis 24 0.545
714
MNN004 Meningothelial Meningioma 25 0.545
715
HRN003 Heroin Dependence 44 0.545
716
GNT019 Giant Cell Myocarditis 29 0.545
717
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.545
718
P ACT105 Acute Mountain Sickness 52 0.545
719
P RSS029 Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha 16 0.545
720
P PRS038 Personality Disorder 65 0.532
721
P SBS003 Substance Abuse 54 0.532
722
MYF001 Myofibroma 42 0.532
723
P EYD002 Eye Disease 57 0.532
724
c HMC039 Hemochromatosis, Type 1 73 0.512
725
GLN010 Glanzmann Thrombasthenia 66 0.512
726
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.512
727
XRP001 Xerophthalmia 42 0.512
728
PRM013 Premature Menopause 57 0.512
729
PLY150 Polykaryocytosis Inducer 29 0.512
730
WND001 Wound Botulism 35 0.512
731
ORG002 Organic Acidemia 43 0.512
732
INT146 Intervertebral Disc Disease 61 0.512
733
PLP001 Pulpitis 48 0.512
734
P TLN014 Tl Antigen 18 0.512
735
KRT001 Keratoconjunctivitis Sicca 49 0.512
736
c INF023 Inflammatory Breast Carcinoma 48 0.512
737
P ICH004 Ichthyosis 56 0.512
738
P MTR003 Mitral Valve Stenosis 53 0.512
739
CHR073 Choreatic Disease 53 0.512
740
EPC002 Epicondylitis 43 0.512
741
CHR096 Chronic Pulmonary Heart Disease 41 0.512
742
SLC006 Silicosis 55 0.512
743
SKN022 Skin Squamous Cell Carcinoma 54 0.512
744
GST007 Gastric Dilatation 29 0.512
745
INC021 Incontinentia Pigmenti 63 0.512
746
c RTN047 Retinitis Pigmentosa 18 45 0.512
747
c RNG019 Ring Chromosome 3 19 0.512
748
OPD006 Opioid Addiction 48 0.512
749
TBR011 Tuberculous Meningitis 48 0.512
750
BRK012 Broken Heart Syndrome 42 0.512
751
ECC004 Eccrine Porocarcinoma 40 0.512
752
P HYP121 Hypoalphalipoproteinemia 42 0.512
753
PNM013 Pneumococcal Meningitis 43 0.512
754
HYP855 Hyperpigmentation of the Skin 26 0.512
755
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.507
756
HYP781 Hypoascorbemia 52 0.507
757
DSS008 Disease of Mental Health 74 0.507
758
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.507
759
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.507
760
NWB001 Newborn Respiratory Distress Syndrome 56 0.507
761
c HPT007 Hepatitis E 50 0.507
762
NRT001 Neurotic Disorder 56 0.507
763
FNG016 Fungal Keratitis 39 0.507
764
HRW001 Hair Whorl 35 0.506
765
c FNC043 Fanconi Anemia, Complementation Group E 62 0.475
766
LMY014 Leiomyoma, Uterine 55 0.475
767
VTM033 Vitamin K Deficiency Bleeding 50 0.475
768
MLT157 Multiple System Atrophy 1 69 0.475
769
CNN001 Cannabis Dependence 38 0.475
770
PLM012 Pulmonary Sarcoidosis 53 0.475
771
DBT002 Diabetic Autonomic Neuropathy 40 0.475
772
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.475
773
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.475
774
CCN002 Cocaine Abuse 49 0.475
775
PLL009 Pellucid Marginal Degeneration 21 0.475
776
CNN002 Cannabis Abuse 44 0.475
777
CRN030 Coronary Stenosis 50 0.474
778
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.453
779
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 0.433
780
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.433
781
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 48 0.433
782
CNR001 Coenurosis 26 0.433
783
c MCR382 Microcephaly 26, Primary, Autosomal Dominant 18 0.433
784
c MCR383 Microcephaly 27, Primary, Autosomal Dominant 12 0.433
786
IMM064 Immunodeficiency, Common Variable, 10 43 0.433
787
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.433
788
P CYS039 Cystic Kidney Disease 52 0.433
789
P MCR010 Microcephaly 59 0.433
790
c PRM212 Primary Microcephaly 40 0.433
791
PST053 Postherpetic Neuralgia 40 0.433
792
RSC001 Rosacea 55 0.433
793
PST021 Postpartum Depression 50 0.433
794
PRN035 Perniosis 27 0.433
795
MYC006 Mycosis Fungoides 65 0.433
796
VCC001 Vaccinia 49 0.425
797
P LNG064 Lung Cancer Susceptibility 3 70 0.418
798
MDD018 Middle East Respiratory Syndrome 44 0.410
799
PPL052 Papillomatosis, Confluent and Reticulated 34 0.410
800
P OVR042 Ovarian Cancer 88 0.403
801
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.396
802
P JBR020 Joubert Syndrome 1 74 0.396
803
c DSB006 Desbuquois Dysplasia 1 48 0.396
804
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.396
805
ABL002 Ablepharon-Macrostomia Syndrome 50 0.396
806
c MCL062 Mucolipidosis Ii Alpha/beta 69 0.396
807
c INF071 Inflammatory Bowel Disease 1 65 0.396
808
IMM166 Immunodeficiency 27a 58 0.396
809
ATX049 Ataxia with Vitamin 3 Deficiency 52 0.396
810
ATM052 Autoimmune Disease 1 36 0.396
811
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.396
812
c SRC023 Sarcoidosis 2 44 0.396
813
FCT002 Factor Xi Deficiency 61 0.396
814
c PSR032 Psoriasis 11 47 0.396
815
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.396
816
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.396
817
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.396
818
ATN013 Autoinflammation, Panniculitis, and Dermatosis Syndrome 48 0.396
819
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.396
820
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.396
821
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.396
822
P PRG092 Pregnancy Loss, Recurrent 1 42 0.396
823
c DRR009 Diarrhea 6 46 0.396
824
c NRP036 Neuropathy, Hereditary Sensory, Type if 33 0.396
825
MYC004 Mycotic Corneal Ulcer 14 0.396
826
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.396
827
c EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 51 0.396
828
P NJM001 Nijmegen Breakage Syndrome 75 0.396
829
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.396
830
c PSR023 Psoriasis 1 52 0.396
831
ARM010 Arima Syndrome 56 0.396
832
ERY003 Erythema Multiforme 56 0.396
833
SVR097 Severe Cutaneous Adverse Reaction 68 0.396
834
c SYS043 Systemic Lupus Erythematosus 1 38 0.396
835
c HYP272 Hypercholesterolemia, Familial, 3 46 0.396
836
URN022 Urinary Tract Infections, Recurrent 27 0.396
837
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.396
838
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.396
839
P PHT010 Photoparoxysmal Response 1 45 0.396
840
ADR038 Adermatoglyphia 51 0.396
841
c BLD140 Blood Group, I System 47 0.396
842
OCL020 Ocular Cicatricial Pemphigoid 52 0.396
843
HYP555 Hypertriglyceridemia, Transient Infantile 38 0.396
844
c CNG413 Congenital Short Bowel Syndrome 42 0.396
845
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.396
846
MCS006 Macs Syndrome 57 0.396
847
c PSR018 Psoriasis 13 40 0.396
848
c PSR028 Psoriasis 7 43 0.396
849
NRL018 Neural Tube Defects, Folate-Sensitive 45 0.396
850
BWN001 Bowen-Conradi Syndrome 54 0.396
851
ACD008 Acid-Labile Subunit Deficiency 52 0.396
852
BLL004 Bullous Keratopathy 47 0.396
853
ACT011 Acute Contagious Conjunctivitis 42 0.396
854
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 30 0.396
855
KRT008 Keratopathy 46 0.396
856
P CRV039 Cervicitis 52 0.396
857
IRR001 Irregular Astigmatism 32 0.396
858
P EHL001 Ehlers-Danlos Syndrome 57 0.396
859
RDN001 Reading Disorder 40 0.396
860
GRN055 Granular Corneal Dystrophy 36 0.396
861
CCT002 Cicatricial Pemphigoid 53 0.396
862
MYF002 Myofascial Pain Syndrome 46 0.396
863
c PSR017 Psoriasis 2 53 0.396
864
MYC088 Mycobacterium Avium Complex Infections 27 0.396
865
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.396
866
FRS019 Farsightedness 35 0.396
867
ATX019 Ataxia with Vitamin E Deficiency 44 0.396
868
PHT003 Phototoxic Dermatitis 27 0.396
869
PRS011 Persian Gulf Syndrome 35 0.396
870
RSP007 Respiratory Distress Syndrome, Infant 40 0.396
871
P BRT047 Brittle Cornea Syndrome 42 0.396
872
CNT060 Central Serous Chorioretinopathy 39 0.396
873
AND005 Androgen Insensitivity Syndrome, Mild 21 0.396
874
CHL079 Children's Interstitial Lung Disease 26 0.396
875
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.396
876
CCN001 Cocaine Dependence 48 0.396
878
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.396
879
NNN007 Non-Involuting Congenital Hemangioma 40 0.396
881
END072 Endotheliitis 36 0.396
882
ERY066 Erythema Multiforme Major 29 0.396
883
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.396
884
CHL065 Cholangiocarcinoma 58 0.395
885
INT079 Intrahepatic Cholangiocarcinoma 51 0.395
886
c WLM018 Wilms Tumor 5 54 0.391
887
P SPR093 Spermatogenic Failure, Y-Linked, 2 32 0.387
888
HYP060 Hyperinsulinism 53 0.387
889
DND003 Dendritic Cell Thymoma 23 0.387
890
c THY086 Thymoma Type B 12 0.387
891
LYM027 Lymphopenia 56 0.379
892
BCK006 Back Pain 43 0.379
893
P PNM007 Pneumonia 64 0.379
894
P HYP076 Hyperthyroidism 53 0.379
895
P GRV001 Graves' Disease 54 0.370
896
THY029 Thyroid Carcinoma 54 0.370
897
c TYP010 Type C Thymoma 25 0.362
898
P AVS003 Avascular Necrosis 41 0.362
899
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.356
900
DNG003 Dengue Disease 65 0.356
901
DNG002 Dengue Hemorrhagic Fever 59 0.356
902
CYS001 Cystic Fibrosis 77 0.353
903
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.353
904
SPL018 Splenomegaly 47 0.353
905
P UVT001 Uveitis 57 0.344
906
IGG001 Iga Glomerulonephritis 50 0.344
907
P ART022 Arthritis 70 0.344
908
c HNT004 Huntington Disease-Like 2 51 0.335
909
PRT013 Portal Hypertension 59 0.335
910
SVR001 Severe Acute Respiratory Syndrome 68 0.335
911
NRM005 Neuromuscular Disease 63 0.335
912
IMM167 Immune Deficiency Disease 77 0.326
913
P CTN015 Cutaneous T Cell Lymphoma 48 0.326
914
P SLM003 Salmonellosis 54 0.326
915
c SCL052 Scleroderma, Familial Progressive 60 0.326
916
IGR001 Ige Responsiveness, Atopic 59 0.326
917
P EPL164 Epilepsy 70 0.326
918
PRS045 Prostatic Hypertrophy 52 0.326
919
BCT004 Bacteriuria 48 0.326
920
CRT016 Carotid Artery Disease 52 0.326
921
RYN005 Raynaud Phenomenon 45 0.326
922
PRS129 Prostatic Hyperplasia, Benign 48 0.316
923
TQP001 Taqi Polymorphism 29 0.316
924
P GRF003 Graft-Versus-Host Disease 71 0.316
925
c CHR098 Chronic Pyelonephritis 34 0.316
926
P ATS364 Autism 72 0.316
927
PRS021 Prostatic Adenoma 43 0.316
928
P OBS001 Obstructive Jaundice 49 0.316
929
P URT039 Urticaria 57 0.316
930
P ART023 Arthropathy 60 0.316
931
HMP009 Haemophilus Influenzae 41 0.316
932
P SCK005 Sickle Cell Disease 56 0.316
933
P FML011 Familial Adenomatous Polyposis 71 0.306
934
P CRD119 Cardiac Arrest 68 0.306
935
c PRG020 Paragangliomas 3 39 0.306
936
CRT013 Carotid Stenosis 51 0.306
937
CHR074 Choriocarcinoma 46 0.306
938
P TRT010 Teratoma 50 0.306
939
MST020 Mast Cell Activation Syndrome 27 0.306
940
ANT024 Anthrax Disease 58 0.306
941
P PRC019 Precocious Puberty 49 0.306
942
ACN019 Acanthamoeba Keratitis 30 0.306
943
GLC003 Glucose Intolerance 53 0.295
944
P THR015 Thrombophilia 51 0.295
945
VRL011 Viral Infectious Disease 60 0.295
946
c PRD040 Periodontitis, Chronic 52 0.285
947
KWS002 Kawasaki Disease 65 0.285
948
MNT001 Mantle Cell Lymphoma 65 0.285
949
OTT002 Otitis Media 71 0.285
950
BRN012 Bronchiolitis Obliterans 56 0.285
951
HRY003 Hairy Cell Leukemia 61 0.285
952
IMM001 Immune-Complex Glomerulonephritis 36 0.285
953
P GND004 Gonadal Dysgenesis 46 0.285
954
GST033 Gestational Diabetes 61 0.285
955
TTN003 Tetanus 64 0.285
956