Search results for NAD

1493 hits were found for NAD

# Family MCID Name MIFTS Score
1
NTR027 Neutrophil Actin Dysfunction 27 16.539
2
P VRT014 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 23 15.044
3
c VRT017 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 22 13.932
4
AGN016 Aging 54 12.771
5
CNG532 Congenital Vertebral-Cardiac-Renal Anomalies Syndrome 17 12.427
6
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 19 11.405
7
PRT037 Pertussis 65 11.153
8
P ENC069 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 1 25 10.880
9
DPH001 Diphtheria 59 10.680
10
ENC066 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 2 25 10.276
11
CHL014 Cholera 62 10.236
12
P HYP769 Hyperlysinemia, Type I 42 9.738
13
FTT001 Fatty Liver Disease 62 8.615
14
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.972
15
HYP066 Hyperglycemia 61 7.172
16
HYP266 Hypoxia 57 7.021
17
HMP009 Haemophilus Influenzae 41 6.843
18
ISC004 Ischemia 61 6.842
19
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 6.396
20
c MCR130 Microvascular Complications of Diabetes 6 41 6.135
21
c MCR120 Microvascular Complications of Diabetes 7 47 6.135
22
c MCR113 Microvascular Complications of Diabetes 3 52 6.135
23
c MCR133 Microvascular Complications of Diabetes 4 41 6.135
24
ANX004 Anoxia 40 6.112
25
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 5.989
26
BRN071 Brain Injury 50 5.855
27
WLL004 Wallerian Degeneration 38 5.768
28
P MYC084 Mycobacterium Tuberculosis 1 68 5.692
29
HLX001 Helix Syndrome 48 5.631
30
P NRB001 Neuroblastoma 66 5.240
31
P ALZ034 Alzheimer Disease 87 5.230
32
CRB004 Cerebral Artery Occlusion 45 5.102
33
ART002 Arts Syndrome 66 5.085
34
NRX001 Neuroaxonal Dystrophy 38 5.070
35
P PNC035 Pancreatic Cancer 86 5.008
36
ATH013 Atherosclerosis Susceptibility 63 4.985
37
P VSC007 Vascular Disease 63 4.956
38
P MYP004 Myopathy 67 4.934
39
c HYP836 Hypercholesterolemia, Familial, 1 73 4.924
40
P HNT016 Huntington Disease 73 4.917
41
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 4.902
42
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.856
43
TRM010 Traumatic Brain Injury 51 4.818
44
47X002 47,xyy 48 4.774
45
GLB002 Glioblastoma 67 4.722
46
P PRP019 Peripheral Nervous System Disease 58 4.592
47
P LTR001 Lateral Sclerosis 58 4.589
48
ALL014 Allergic Encephalomyelitis 34 4.551
49
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.495
50
GLM045 Glioma 63 4.471
51
P NRP001 Neuropathy 60 4.446
52
GLL048 Glial Tumor 52 4.434
53
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.281
54
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.281
55
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.281
56
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.281
57
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.281
58
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.281
59
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.281
60
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.281
61
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.281
62
P MTC069 Mitochondrial Disorders 57 4.263
63
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.260
64
LPD008 Lipid Metabolism Disorder 62 4.205
65
PRM329 Premature Aging 36 4.150
66
P LVR013 Liver Disease 69 4.128
67
P MSC005 Muscular Dystrophy 67 4.111
68
P PRS040 Prostate Cancer 95 4.059
69
P RTN016 Retinal Degeneration 52 4.028
70
CNG034 Congestive Heart Failure 69 3.979
71
P LNG032 Lung Cancer 98 3.948
72
GLC003 Glucose Intolerance 54 3.945
73
P MTC133 Mitochondrial Myopathy 50 3.868
74
c MCR115 Microvascular Complications of Diabetes 5 65 3.839
75
P SKN015 Skin Carcinoma 71 3.780
76
P PLL002 Pellagra 46 3.774
77
P PLM036 Pulmonary Fibrosis 66 3.728
78
48X005 48,xyyy 39 3.714
79
P OVR042 Ovarian Cancer 88 3.643
80
MYL069 Myeloma, Multiple 77 3.635
81
c LKM061 Leukemia, Acute Myeloid 83 3.629
82
CYT002 Cytokine Deficiency 43 3.628
83
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.609
84
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.603
85
P BRS047 Breast Cancer 98 3.588
86
P LNG064 Lung Cancer Susceptibility 3 70 3.552
87
PRT251 Proteinuria, Chronic Benign 57 3.541
88
P LKM062 Leukemia, Acute Lymphoblastic 69 3.523
89
P LKM002 Leukemia 67 3.514
90
CND006 Candida Glabrata 30 3.514
91
P MLN008 Melanoma 76 3.505
92
MTC005 Mitochondrial Metabolism Disease 45 3.492
93
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.472
94
P PRK039 Parkinsonism 55 3.469
95
P CCK001 Cockayne Syndrome 68 3.445
96
c ATR087 Atrial Standstill 1 74 3.443
97
TXC005 Toxic Shock Syndrome 62 3.442
98
P LKM071 Leukemia, Chronic Lymphocytic 75 3.434
99
P LCT001 Lactic Acidosis 51 3.407
100
INS001 Insulinoma 59 3.399
101
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.312
102
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.291
103
P MLT020 Multiple Sclerosis 79 3.287
104
c TYP009 Type 2 Diabetes Mellitus 92 3.287
105
HPT022 Hepatoblastoma 54 3.260
106
P KLZ004 Kala-Azar 1 41 3.231
107
LSH001 Leishmaniasis 64 3.231
108
P ATX030 Ataxia-Telangiectasia 80 3.231
109
TLN003 Telangiectasis 51 3.231
110
HYP060 Hyperinsulinism 54 3.215
111
P DMN002 Dementia 66 3.188
112
HYP056 Hypoglycemia 65 3.188
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.162
114
ART140 Arteries, Anomalies of 53 3.151
115
STR067 Stroke, Ischemic 80 3.151
116
c TYP008 Type 1 Diabetes Mellitus 70 3.146
117
P HPT023 Hepatocellular Carcinoma 96 3.136
118
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.125
119
LPP008 Lipoprotein Quantitative Trait Locus 65 3.123
120
P PRK057 Parkinson Disease, Late-Onset 80 3.103
122
c SML038 Small Cell Cancer of the Lung 69 3.082
123
P GST053 Gastric Cancer 83 3.058
124
ALC007 Alcohol Dependence 66 3.050
125
c ACT071 Acute Kidney Failure 60 3.014
126
OST159 Osteogenic Sarcoma 66 2.981
127
P BCL017 B-Cell Lymphoma 59 2.978
128
P BLD134 Bladder Cancer 79 2.966
129
HMC014 Homocysteinemia 52 2.965
130
MTB004 Metabolic Acidosis 48 2.938
131
P PHC003 Pheochromocytoma 69 2.917
132
ADR040 Adrenal Gland Pheochromocytoma 46 2.917
133
P ENC018 Encephalopathy 62 2.904
134
MLD018 Mild Cognitive Impairment 48 2.888
135
P HML002 Hemolytic Anemia 62 2.859
136
P RNV001 Renovascular Hypertension 49 2.857
137
DBT010 Diabetic Neuropathy 54 2.828
138
HRW001 Hair Whorl 35 2.827
139
CHG001 Chagas Disease 66 2.795
141
ATM095 Autoimmune Disease 61 2.743
142
P MSC003 Muscular Atrophy 52 2.737
143
P BRS044 Breast Adenocarcinoma 58 2.705
144
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.696
145
ATS010 Autosomal Recessive Disease 42 2.695
146
PST092 Posttransplant Acute Limbic Encephalitis 28 2.695
147
P FBR017 Fibrosarcoma 56 2.695
148
P RTN018 Retinal Disease 53 2.673
149
MSC007 Muscle Hypertrophy 64 2.660
150
P CHR012 Chronic Granulomatous Disease 69 2.660
151
BRK010 Burkitt Lymphoma 66 2.659
152
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.659
153
P ALC033 Alcohol Use Disorder 61 2.654
154
c HPT001 Hepatitis C 62 2.654
155
P KDN018 Kidney Disease 72 2.640
156
XRD010 Xeroderma Pigmentosum, Variant Type 73 2.623
157
HDN002 Head Injury 44 2.623
158
HGH043 High Grade Glioma 45 2.622
159
PHR003 Pharyngitis 58 2.604
160
ESP021 Esophageal Cancer 83 2.600
161
c HPT073 Hepatitis C Virus 71 2.592
162
LBR036 Leber Plus Disease 66 2.592
163
c DLT002 Dilated Cardiomyopathy 78 2.583
164
CRB039 Cerebrovascular Disease 66 2.573
165
P MYL006 Myeloid Leukemia 61 2.560
166
END057 Endometrial Cancer 72 2.543
167
P ADN016 Adenocarcinoma 63 2.538
168
P CLR023 Colorectal Cancer 100 2.528
169
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.503
170
APP015 Apparent Mineralocorticoid Excess 57 2.503
171
P DBT009 Diabetes Mellitus 67 2.503
172
SCH014 Schistosomiasis 56 2.503
173
P SPP010 Suppressor of Tumorigenicity 3 51 2.475
174
P HRT032 Heart Disease 81 2.465
175
P PLM037 Pulmonary Hypertension 72 2.462
176
P PRD008 Periodontitis 64 2.434
177
c ACT027 Acute Pancreatitis 60 2.428
178
CHL123 Chlamydia 58 2.428
179
DPR016 Depression 65 2.404
180
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.403
181
c PRC016 Pre-Eclampsia 65 2.403
182
ATN004 Autonomic Neuropathy 42 2.399
183
PPL052 Papillomatosis, Confluent and Reticulated 34 2.393
184
c HYP595 Hypertension, Essential 85 2.393
185
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 2.393
186
MLR004 Malaria 80 2.392
187
CRC021 Carcinosarcoma 64 2.392
188
WHP002 Whiplash 36 2.373
189
P BND020 Bone Disease 59 2.372
190
P MYC007 Myocardial Infarction 70 2.358
191
P GST044 Gastritis 55 2.353
192
INS024 Insulin-Like Growth Factor I 78 2.339
193
P DRM053 Dermatitis, Atopic 65 2.322
194
LNG099 Lung Disease 62 2.322
195
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.322
196
LGH007 Leigh Syndrome 70 2.314
197
CVD001 Covid-19 57 2.303
198
MNT002 Mental Depression 57 2.300
199
CRD132 Cardiac Conduction Defect 60 2.285
200
ALL029 Allergic Disease 59 2.273
201
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 2.273
202
STN013 Stenotrophomonas Maltophilia Infection 26 2.266
203
CLN015 Colon Adenocarcinoma 65 2.266
204
OST012 Osteoarthritis 77 2.247
205
SLP001 Sleeping Sickness 56 2.247
206
P INF037 Inflammatory Bowel Disease 53 2.231
207
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.220
208
c SCL052 Scleroderma, Familial Progressive 61 2.209
209
LMB062 Limb Ischemia 55 2.209
210
BRR014 Barrett Esophagus 66 2.209
211
RTN020 Retinal Vascular Disease 46 2.209
212
P PNC044 Pancreatitis 61 2.209
213
P RCT021 Rectum Cancer 54 2.209
214
PLY100 Polyploidy 36 2.205
215
P GLM040 Glioma Susceptibility 1 71 2.205
216
END086 End Stage Renal Disease 52 2.205
217
CRV035 Cervical Cancer 73 2.172
218
SJG002 Sjogren-Larsson Syndrome 54 2.169
219
NNL006 Non-Alcoholic Steatohepatitis 54 2.169
220
P GLC113 Galactosemia I 66 2.169
221
PRT036 Peritonitis 65 2.169
222
IRN002 Iron Metabolism Disease 57 2.169
223
CLT003 Colitis 63 2.169
224
PHN003 Phenylketonuria 76 2.169
225
PNC129 Pancreatic Adenocarcinoma 65 2.169
226
c CHR684 Chronic Kidney Disease 69 2.157
227
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.128
228
ACT098 Acute Erythroid Leukemia 55 2.128
229
LYM027 Lymphopenia 56 2.128
230
P SCK005 Sickle Cell Disease 56 2.128
231
NCR007 Necrotizing Fasciitis 49 2.125
232
FSC004 Fasciitis 49 2.125
233
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.098
234
MSC157 Muscular Dystrophy, Duchenne Type 79 2.096
235
SPN035 Spindle Cell Sarcoma 54 2.096
236
CNS004 Constipation 56 2.096
237
SRC014 Sarcoma 65 2.096
238
P INF032 Infertility 57 2.087
239
HMN044 Human Immunodeficiency Virus Type 1 78 2.059
240
DFC004 Deficiency Anemia 74 2.059
241
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 2.059
242
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.059
243
DSS032 Disease by Infectious Agent 55 2.059
244
DMY004 Demyelinating Disease 50 2.059
245
TRN015 Transient Cerebral Ischemia 63 2.050
246
P HYP076 Hyperthyroidism 53 2.050
247
P GLM007 Glomerulonephritis 60 2.050
248
SPN186 Spinal Cord Injury 61 2.043
249
P CRN300 Coronary Heart Disease 1 73 2.043
250
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 2.043
251
VSC003 Visceral Leishmaniasis 55 2.043
252
DNT012 Dental Caries 53 2.043
253
IMP005 Impotence 52 2.043
254
SVR004 Severe Combined Immunodeficiency 72 2.043
255
P DRR001 Diarrhea 55 2.043
256
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 2.043
257
KRN002 Kearns-Sayre Syndrome 63 2.041
258
c OPT053 Optic Atrophy 1 62 2.020
259
P BRG001 Brugada Syndrome 69 2.020
260
BNR002 Bone Resorption Disease 47 2.020
261
ANT024 Anthrax Disease 58 2.020
262
P HPT021 Hepatitis 69 2.020
263
STR077 Streptococcal Toxic-Shock Syndrome 35 2.008
264
P LYM118 Lymphoma 67 1.999
265
GST040 Gastric Adenocarcinoma 67 1.999
266
P NTR004 Neutropenia 63 1.999
267
P CRD246 Cardiovascular System Disease 56 1.999
268
P MYC008 Myocarditis 59 1.999
269
c MJR022 Major Affective Disorder 8 38 1.980
270
c MJR024 Major Affective Disorder 9 41 1.980
271
P BPL003 Bipolar Disorder 56 1.980
272
P ATR011 Atrial Fibrillation 66 1.953
273
c ACT073 Acute Leukemia 58 1.953
274
P PRN023 Prion Disease 60 1.953
275
CHL065 Cholangiocarcinoma 58 1.949
276
INT079 Intrahepatic Cholangiocarcinoma 51 1.949
277
c PCH010 Pachyonychia Congenita 3 43 1.940
278
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.940
279
P THR014 Thrombocytopenia 66 1.940
280
ART016 Aortic Aneurysm 68 1.940
281
MLG169 Malignant Astrocytoma 57 1.940
282
CHL068 Cholestasis 61 1.940
283
HYP014 Hyperuricemia 51 1.940
284
SPL018 Splenomegaly 49 1.940
285
BRN004 Brain Edema 54 1.916
286
c ATS007 Autism Spectrum Disorder 72 1.905
287
P PSR002 Psoriasis 63 1.898
288
PST011 Pustulosis of Palm and Sole 52 1.898
289
RCK004 Rickets 68 1.898
290
c ACT075 Acute Myocardial Infarction 56 1.895
291
HRN029 Hearing Loss, Noise-Induced 37 1.856
292
ULC004 Ulcerative Colitis 74 1.856
293
HYP005 Hypokalemia 55 1.856
294
DWR001 Dwarfism 44 1.856
296
P SNS001 Sensorineural Hearing Loss 59 1.838
297
LYM019 Lymphosarcoma 46 1.836
298
LNG031 Lung Benign Neoplasm 51 1.836
299
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.818
300
P ADL010 Adult Respiratory Distress Syndrome 71 1.818
301
STT001 Status Epilepticus 59 1.818
302
P HYP111 Hyperprolinemia 45 1.810
303
OCL069 Ocular Motor Apraxia 57 1.810
304
P LPS004 Lupus Erythematosus 61 1.810
305
NRM005 Neuromuscular Disease 63 1.810
306
P HYP086 Hypothyroidism 69 1.810
307
P ECL001 Eclampsia 52 1.810
308
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 1.805
309
P ATS364 Autism 69 1.804
310
THY029 Thyroid Carcinoma 51 1.804
311
ACT119 Acute Promyelocytic Leukemia 62 1.768
312
P URN019 Urinary Tract Infection 49 1.764
313
SCK003 Sickle Cell Anemia 74 1.764
314
P HYP750 Hypertriglyceridemia, Familial 62 1.764
315
P KRN004 Kernicterus 46 1.764
316
P ICH004 Ichthyosis 56 1.764
317
ANR040 Aneurysm 61 1.764
318
LYM133 Lymphoma, Hodgkin, Classic 74 1.750
319
DBT002 Diabetic Autonomic Neuropathy 41 1.749
320
NRR001 Neuroretinitis 42 1.717
321
ARG004 Argyria 26 1.717
322
RTN023 Retinitis 46 1.717
323
BLR008 Bilirubin Metabolic Disorder 57 1.717
324
PTT037 Pituitary Tumors 44 1.717
325
P MJR001 Major Depressive Disorder 68 1.714
326
RNL077 Renal Fibrosis 46 1.714
327
CHR005 Chorioamnionitis 50 1.694
328
HLC007 Helicobacter Pylori Infection 67 1.694
329
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.694
330
CHR074 Choriocarcinoma 46 1.694
331
BRN056 Bronchopulmonary Dysplasia 56 1.694
332
ANX010 Anxiety 70 1.678
333
P THL005 Thalassemia 56 1.667
334
P ANP001 Anaplastic Large Cell Lymphoma 61 1.667
335
c LBR019 Leber Congenital Amaurosis 9 44 1.667
336
TRY001 Trypanosomiasis 50 1.667
337
RTN003 Retinal Ischemia 49 1.667
338
KRT009 Keratosis 53 1.667
339
SQM006 Squamous Cell Carcinoma 60 1.667
340
P FML187 Familial Hypertension 34 1.667
341
CHR178 Chromosomal Triplication 34 1.667
342
P SZR006 Seizure Disorder 70 1.641
343
c EXD008 Exudative Vitreoretinopathy 1 71 1.634
344
MYL009 Myelodysplastic Syndrome 67 1.634
345
P CYS018 Cystitis 59 1.634
346
P GRV001 Graves' Disease 55 1.634
347
PRS045 Prostatic Hypertrophy 53 1.634
348
GRN017 Granulocytopenia 42 1.634
349
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.616
350
HYP017 Hypophosphatemia 49 1.616
351
WRN001 Werner Syndrome 69 1.616
352
MTC004 Mitochondrial Encephalomyopathy 42 1.616
353
ADN018 Adenoma 59 1.616
354
PRT013 Portal Hypertension 59 1.616
355
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.616
356
c RNG024 Ring Chromosome 8 28 1.616
357
P DYS154 Dystonia 64 1.603
358
ANG054 Angina Pectoris 66 1.570
359
PRS021 Prostatic Adenoma 43 1.570
360
P PLY011 Polycystic Ovary Syndrome 57 1.570
361
BCT022 Bacterial Infectious Disease 56 1.565
362
P CTR002 Cataract 60 1.565
363
P MTH007 Methemoglobinemia 46 1.565
364
LSC001 Lesch-Nyhan Syndrome 62 1.562
365
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 1.562
366
THL010 Thalassemia Minor 32 1.562
367
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.562
368
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.562
369
P MPL001 Maple Syrup Urine Disease 70 1.562
370
URT049 Urate Oxidase, Pseudogene 24 1.562
371
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 1.562
372
SKN016 Skin Disease 63 1.562
373
P UVT001 Uveitis 57 1.562
374
P HYP061 Hypertrophic Cardiomyopathy 69 1.562
375
GLS001 Gliosarcoma 64 1.562
376
P RHN004 Rhinitis 57 1.562
377
P KDN017 Kidney Cancer 61 1.562
378
P TCD001 Tic Disorder 49 1.562
379
c HPT016 Hepatitis B 62 1.562
380
CRB090 Cerebral Hypoxia 42 1.562
381
BCK006 Back Pain 47 1.562
382
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 1.525
383
LNG108 Langerhans Cell Histiocytosis 58 1.525
384
P EPL164 Epilepsy 68 1.525
385
P OPT006 Optic Nerve Disease 58 1.525
386
HST010 Histiocytosis 49 1.525
387
NRM022 Neurometabolic Disease 24 1.505
388
ALL003 Allergic Rhinitis 67 1.505
389
P AST005 Asthma 76 1.505
390
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.505
391
c PRM108 Primary Progressive Multiple Sclerosis 51 1.505
392
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.505
393
P HYP733 Hypercalciuria, Absorptive, 2 45 1.505
394
ORL015 Oral Squamous Cell Carcinoma 43 1.505
395
P ATR005 Atrophic Gastritis 50 1.505
396
PLR005 Pleuropneumonia 33 1.505
397
GST023 Gastric Ulcer 52 1.505
398
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.501
399
P SCH015 Schizophrenia 74 1.501
400
HMT002 Hematologic Cancer 61 1.501
401
ART074 Aortic Dissection 53 1.484
402
P ART022 Arthritis 71 1.484
403
P CRD119 Cardiac Arrest 67 1.484
404
PRQ002 Paraquat Poisoning 28 1.445
405
CRD223 Cardiac Arrhythmia 63 1.445
406
HMN047 Human Cytomegalovirus Infection 57 1.445
407
P XNT004 Xanthinuria 37 1.445
408
P AMY004 Amyloidosis 70 1.445
409
VCC001 Vaccinia 47 1.445
410
DRM006 Dermatitis 62 1.445
412
PTH003 Pathologic Nystagmus 52 1.445
413
c HRD142 Hereditary Xanthinuria 43 1.445
414
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.443
415
P TRM003 Tremor 48 1.443
416
PSY004 Psychotic Disorder 66 1.443
417
c SPR086 Spermatogenic Failure 3 46 1.426
418
c LNG109 Lung Cancer Susceptibility 1 26 1.426
419
AMN003 Amnestic Disorder 54 1.426
420
CTR172 Citrullinemia, Classic 65 1.399
421
ENT011 Enterocolitis 55 1.399
422
ECH003 Echinococcosis 53 1.399
423
LVR012 Liver Cirrhosis 63 1.399
424
P PLY019 Polyneuropathy 52 1.399
425
MNT001 Mantle Cell Lymphoma 67 1.381
426
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.381
427
c LNG048 Long Qt Syndrome 3 53 1.381
428
GLB001 Gilbert Syndrome 53 1.381
429
MDD018 Middle East Respiratory Syndrome 44 1.381
430
EXT007 Extracutaneous Mastocytoma 38 1.381
431
c FML191 Familial Long Qt Syndrome 55 1.381
432
MST004 Mast Cell Neoplasm 42 1.381
433
c BSL007 Basal Cell Carcinoma 68 1.381
434
P LNG028 Long Qt Syndrome 64 1.381
435
P CRN026 Corneal Edema 42 1.381
436
P SBS003 Substance Abuse 54 1.381
437
P CTS001 Cutis Laxa 65 1.381
438
P ART021 Arteriosclerosis 54 1.381
439
MSL001 Measles 61 1.381
440
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 1.355
441
HYP025 Hyperphosphatemia 48 1.355
442
HPT004 Hepatic Coma 43 1.355
443
URT010 Ureteral Obstruction 45 1.355
444
BRN024 Bronchitis 67 1.355
445
c INH020 Inherited Metabolic Disorder 48 1.355
446
STM007 Stomatitis 54 1.355
447
PRS129 Prostatic Hyperplasia, Benign 49 1.312
448
c SVR003 Severe Congenital Neutropenia 59 1.312
449
P RHB003 Rhabdomyosarcoma 66 1.312
450
P GRF003 Graft-Versus-Host Disease 71 1.312
451
DYS015 Dysentery 50 1.312
452
QFV001 Q Fever 62 1.312
453
c SVR005 Severe Pre-Eclampsia 50 1.312
454
P MNN013 Meningitis 65 1.312
455
SPS057 Spasticity 42 1.309
456
DWN001 Down Syndrome 70 1.309
457
P RTN024 Retinoblastoma 73 1.309
458
HPT019 Hepatic Encephalopathy 59 1.309
459
P EYD002 Eye Disease 57 1.309
460
P MTR014 Motor Neuron Disease 65 1.309
461
P FRD001 Friedreich Ataxia 61 1.286
462
P RTN008 Retinitis Pigmentosa 80 1.261
463
P CND004 Candidiasis 58 1.261
464
ASP007 Aspiration Pneumonia 49 1.261
465
PLR008 Pleurisy 50 1.261
466
HRY003 Hairy Cell Leukemia 61 1.261
467
P ENC004 Encephalitis 61 1.261
468
HST006 Histidinemia 48 1.250
469
PNM013 Pneumococcal Meningitis 43 1.238
470
P MYS005 Myositis 56 1.238
471
P CHN012 Chondrosarcoma 57 1.238
472
PRM317 Primary Qualitative or Quantitative Defects of Alpha-Dystroglycan 8 1.238
473
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 1.238
474
P RBL001 Rubella 58 1.238
475
QLT016 Qualitative or Quantitative Defects of Protein Involved in O-Glycosylation of Alpha-Dystroglycan 6 1.238
476
PLM001 Pulmonary Tuberculosis 69 1.238
477
MLT006 Multidrug-Resistant Tuberculosis 47 1.238
478
CHL061 Childhood Leukemia 47 1.238
479
LYM040 Lymphoblastic Lymphoma 53 1.238
480
END085 Endometrial Serous Adenocarcinoma 43 1.238
481
P DYS007 Dyskeratosis Congenita 67 1.238
482
c ACT135 Acute Graft Versus Host Disease 51 1.238
484
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 1.238
485
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 1.212
486
TTR011 Tetraploidy 43 1.212
487
P HRS035 Hirschsprung Disease 1 66 1.212
488
RBF001 Riboflavin Deficiency 49 1.212
489
P ACN011 Acne 57 1.212
490
HMS001 Hemosiderosis 48 1.212
491
CRT015 Carotid Artery Occlusion 45 1.212
492
P TMP001 Temporal Lobe Epilepsy 49 1.212
493
PLM010 Pulmonary Edema 55 1.212
494
HRT031 Hartnup Disorder 52 1.205
495
CRT020 Cortisone Reductase Deficiency 34 1.205
496
LCT008 Lactate Dehydrogenase Deficiency 14 1.205
497
P TRN020 Turner Syndrome 67 1.179
498
P RHM011 Rheumatoid Arthritis 82 1.160
499
c SYS001 Systemic Lupus Erythematosus 87 1.160
500
c LKM063 Leukemia, Chronic Myeloid 71 1.160
501
P HRP006 Herpes Simplex 65 1.160
502
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.160
503
TTN003 Tetanus 65 1.160
504
P ALB003 Albinism-Deafness Syndrome 34 1.155
505
ASP030 Aspirin Resistance 40 1.155
506
P ADV001 Advanced Sleep Phase Syndrome 41 1.155
507
CHK001 Chikungunya 60 1.155
508
P XRD029 Xeroderma Pigmentosum, Complementation Group a 56 1.155
509
c LKM055 Leukemia, Acute Lymphoblastic 2 18 1.155
510
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 31 1.155
511
CHD001 Chediak-Higashi Syndrome 67 1.155
512
c CCK008 Cockayne Syndrome a 59 1.155
513
INC002 Inclusion Body Myositis 57 1.155
514
CLR109 Colorectal Adenocarcinoma 50 1.155
516
P HML001 Hemolytic-Uremic Syndrome 52 1.155
517
INT007 Intermediate Coronary Syndrome 54 1.155
518
c VRL010 Viral Hepatitis 53 1.155
519
NPH009 Nephrolithiasis 54 1.155
520
AML001 Amelanotic Melanoma 37 1.155
521
P MMP001 Mumps 57 1.155
522
GTR002 Goiter 53 1.155
523
INT066 Interstitial Lung Disease 60 1.155
524
P OBS001 Obstructive Jaundice 48 1.155
525
CRD016 Cardiac Rupture 34 1.155
526
EWN003 Ewing Sarcoma 70 1.106
527
EPL131 Epilepsy, Pyridoxine-Dependent 45 1.106
528
URM002 Uremia 47 1.106
529
CHR066 Chronic Fatigue Syndrome 60 1.106
530
P RRH023 Rare Hereditary Hemochromatosis 54 1.106
531
GT001 Gout 64 1.106
532
GST045 Gastroenteritis 58 1.106
533
P HYP265 Hypotonia 42 1.106
534
ATN005 Autonomic Dysfunction 46 1.106
535
SRC027 Sarcoma, Synovial 58 1.061
536
RTN017 Retinal Detachment 60 1.061
537
P APL001 Aplastic Anemia 73 1.061
538
CHR100 Chronic Ulcer of Skin 57 1.061
539
P PRG013 Paraganglioma 57 1.061
540
CLR108 Colorectal Adenoma 64 1.061
541
P PLY006 Polydactyly 59 1.061
542
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.061
543
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.061
544
P HMC002 Homocystinuria 53 1.061
545
IMP004 Impetigo 48 1.061
547
DNG003 Dengue Disease 65 1.061
548
CRV040 Cervix Carcinoma 50 1.061
549
ONC002 Onchocerciasis 51 1.061
550
MCR013 Microphthalmia 60 1.061
551
P CWD010 Cowden Syndrome 70 1.061
552
CHR073 Choreatic Disease 54 1.061
553
ADR022 Adrenomyeloneuropathy 39 1.050
554
GLM044 Glomerular Disease 35 1.050
555
c ACT134 Acute Liver Failure 59 1.050
556
FRN006 Frontotemporal Dementia 68 1.050
557
ADR007 Adrenoleukodystrophy 73 1.050
558
P WSK001 Wiskott-Aldrich Syndrome 72 1.050
559
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.050
560
IMM167 Immune Deficiency Disease 78 1.050
561
GNG002 Ganglioneuroma 52 1.050
562
ALV002 Alveolar Echinococcosis 57 1.050
563
c HRD010 Hereditary Spastic Paraplegia 66 1.050
564
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.050
565
P RNL015 Renal Hypertension 45 1.050
566
P CNJ013 Conjunctivitis 66 1.050
567
GNG005 Gangliocytoma 55 1.050
568
LST001 Listeriosis 59 1.050
569
c RNG015 Ring Chromosome 2 22 1.050
570
c FNC027 Fanconi Anemia, Complementation Group a 81 0.994
571
TRD006 Tardive Dyskinesia 53 0.994
572
P NSP012 Nasopharyngeal Carcinoma 61 0.990
573
MTH071 Methane Production 25 0.990
574
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.990
575
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.990
576
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.990
577
APR001 Apraxia 52 0.990
578
RFS006 Refsum Disease, Classic 63 0.990
579
P STR020 Strabismus 56 0.990
580
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.990
581
PRX001 Peroxisomal Disease 46 0.990
582
MCH006 Mechanical Strabismus 40 0.990
583
ALL006 Allergic Asthma 56 0.990
584
P HYP098 Hypereosinophilic Syndrome 66 0.990
585
SVR001 Severe Acute Respiratory Syndrome 67 0.990
586
OVR063 Overnutrition 42 0.990
587
P INF038 Influenza 68 0.990
588
MDD011 Mood Disorder 62 0.990
589
LKS001 Leukostasis 41 0.990
590
c JVN010 Juvenile Rheumatoid Arthritis 66 0.990
591
ATX019 Ataxia with Vitamin E Deficiency 44 0.990
592
ORL011 Oral Cancer 60 0.990
593
CRT033 Corticobasal Degeneration 47 0.990
594
P NRV007 Nervous System Disease 67 0.990
595
CRC014 Carcinoid Tumors, Intestinal 46 0.950
596
PLY150 Polykaryocytosis Inducer 29 0.950
597
HMR023 Hemorrhagic Cystitis 43 0.950
598
WLK001 Walker-Warburg Syndrome 62 0.950
600
c PNC106 Pancreatic Agenesis 1 51 0.950
601
c CCK007 Cockayne Syndrome B 56 0.950
602
THY111 Thyroid Carcinoma, Familial Medullary 67 0.950
603
c SPN294 Spinocerebellar Ataxia 1 53 0.950
604
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.950
605
P MYP006 Myopia 56 0.950
606
SKN019 Skin Melanoma 71 0.950
607
THY125 Thyroid Gland Medullary Carcinoma 48 0.950
608
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.950
609
PPT005 Peptic Ulcer Disease 58 0.950
610
c ACT004 Acute Diarrhea 40 0.950
611
P ESP024 Esophagitis 60 0.950
612
PRM236 Primary Biliary Cholangitis 60 0.950
613
EXS001 Exostosis 49 0.950
614
P INT143 Interstitial Cystitis 60 0.950
615
TXC004 Toxic Diffuse Goiter 23 0.950
616
P MTC010 Mitochondrial Dna Depletion Syndrome 47 0.950
617
ALC005 Alcoholic Pancreatitis 38 0.950
618
ANT019 Anterograde Amnesia 38 0.950
619
PNC034 Pancreas Disease 50 0.950
620
ENT004 Enthesopathy 51 0.950
621
P NRF002 Neurofibromatosis 57 0.950
622
PRS119 Persistent Genital Arousal Disorder 18 0.950
623
SPS019 Spastic Paraparesis 38 0.926
624
P MYS003 Myasthenia Gravis 68 0.926
625
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.926
626
OBS002 Obsessive-Compulsive Disorder 68 0.926
627
P OST002 Osteoporosis 76 0.926
628
CYS001 Cystic Fibrosis 78 0.926
629
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.926
630
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.926
631
P PLY014 Polycystic Kidney Disease 69 0.926
632
P CTN015 Cutaneous T Cell Lymphoma 48 0.926
633
THR024 Thrombosis 56 0.926
634
c THY071 Thyroid Dyshormonogenesis 1 31 0.926
635
KPS004 Kaposi Sarcoma 77 0.926
636
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.926
637
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.926
638
c SPN291 Spinocerebellar Ataxia 7 53 0.926
639
PNG002 Pain Agnosia 51 0.926
640
c CHR418 Chronic Leukemia 48 0.926
641
P ZLL001 Zellweger Syndrome 65 0.926
642
CHL045 Choline Deficiency Disease 39 0.926
643
FCL014 Focal Epilepsy 53 0.926
644
P END044 Endometriosis 62 0.926
645
HPT014 Hepatorenal Syndrome 49 0.926
646
LYM017 Lyme Disease 62 0.926
647
ART004 Aortic Atherosclerosis 47 0.926
648
URN010 Urinary Tract Obstruction 55 0.926
649
PRP030 Purpura 54 0.926
650
P PRM002 Primary Hyperoxaluria 65 0.926
651
SPS003 Spastic Diplegia 53 0.926
652
IRR002 Irritable Bowel Syndrome 65 0.926
653
HML018 Homologous Wasting Disease 21 0.926
654
MYT011 Myotonia 39 0.926
655
OVR094 Ovarian Epithelial Cancer 39 0.926
656
ALC006 Alcoholic Hepatitis 61 0.924
657
PST021 Postpartum Depression 50 0.857
658
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.857
659
PHS027 Phosphoglycoprotein 1 15 0.857
660
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.857
661
DFF005 Diffuse Large B-Cell Lymphoma 54 0.857
662
BCT021 Bacterial Sepsis 43 0.857
663
c THY056 Thyroid Dyshormonogenesis 3 31 0.857
664
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.857
665
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.857
666
P TRT019 Torticollis 47 0.857
667
ORG002 Organic Acidemia 44 0.857
668
c RTN130 Retinitis Pigmentosa 46 40 0.857
669
CRH001 Crohn's Disease 80 0.857
670
AVN001 Avian Influenza 61 0.857
671
NRM001 Neuromyelitis Optica 61 0.857
672
ACH005 Achalasia 55 0.857
673
P MLG056 Malignant Hyperthermia 66 0.857
674
CRB001 Cerebral Lymphoma 36 0.857
675
P PSD015 Pseudohypoparathyroidism 55 0.857
676
OST003 Osteonecrosis 61 0.857
677
BRN028 Brain Cancer 74 0.857
678
P MLN007 Male Infertility 56 0.857
679
P OPT009 Optic Neuritis 57 0.857
680
P GLL022 Guillain-Barre Syndrome 60 0.857
681
c ACT068 Acute Cystitis 61 0.857
682
NRT004 Neuritis 53 0.857
683
GST033 Gestational Diabetes 61 0.857
684
P MCR010 Microcephaly 60 0.857
685
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.857
686
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.857
687
P BNG032 Benign Mesothelioma 53 0.857
688
BRN002 Bronchiolitis 57 0.857
689
GST037 Gastroparesis 52 0.857
690
DBT007 Diabetic Cataract 36 0.857
691
SCL003 Social Phobia 48 0.857
692
DBT004 Diabetic Polyneuropathy 50 0.857
693
ACT200 Acute Monoblastic Leukemia 41 0.857
694
c LKM005 Leukemia, T-Cell, Chronic 34 0.857
695
RFR010 Refractory Anemia 49 0.805
696
PRK088 Parkinson Disease, Mitochondrial 19 0.805
697
END062 Endometrial Hyperplasia 48 0.805
698
c MCR245 Microphthalmia, Syndromic 8 46 0.805
699
PPL035 Papillary Thyroid Microcarcinoma 39 0.805
701
TLC001 Telecanthus 35 0.805
702
DGT002 Digital Clubbing, Isolated Congenital 26 0.805
703
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.805
704
P BLD062 Bile Duct Cancer 67 0.805
705
CRN030 Coronary Stenosis 50 0.805
706
IGG001 Iga Glomerulonephritis 50 0.805
707
ACR014 Acral Lentiginous Melanoma 52 0.805
708
PLM031 Poliomyelitis 63 0.805
709
RHM001 Rheumatic Fever 59 0.805
710
TRN007 Transsexualism 39 0.805
711
MYL078 Myelodysplastic Syndrome with Single Lineage Dysplasia 10 0.805
712
c ART068 Aortic Aneurysm, Familial Thoracic 2 33 0.782
713
c THY107 Thymoma, Familial 42 0.782
714
P LPR021 Leprosy 3 71 0.782
715
P MTR004 Maturity-Onset Diabetes of the Young 68 0.782
716
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.782
717
c MGR028 Migraine with or Without Aura 1 64 0.782
718
PRP027 Peripheral Vascular Disease 71 0.782
719
PRP080 Peripheral Artery Disease 54 0.782
720
P SLP006 Sleep Apnea 69 0.782
721
P EXN002 Exanthem 58 0.782
722
P PRS049 Persistent Mullerian Duct Syndrome 52 0.782
723
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.782
724
c HYP602 Hyperoxaluria, Primary, Type Ii 49 0.782
725
c BRN108 Branchiootic Syndrome 1 62 0.782
726
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.782
727
VRC005 Varicose Veins 60 0.782
728
PHB003 Phobia, Specific 44 0.782
729
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.782
730
ACT003 Acute Kidney Tubular Necrosis 46 0.782
731
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.782
732
CRV002 Cervix Uteri Carcinoma in Situ 47 0.782
733
DGN001 Degenerative Disc Disease 49 0.782
734
ADN001 Adenosine Deaminase Deficiency 59 0.782
735
P PNC025 Panic Disorder 52 0.782
736
P MNC007 Monocytic Leukemia 47 0.782
737
P MMB011 Membranous Nephropathy 50 0.782
738
TCK001 Tick-Borne Encephalitis 59 0.782
739
P CHR071 Charcot-Marie-Tooth Disease 64 0.782
740
SPN020 Spondylosis 46 0.782
741
P BRB001 Beriberi 44 0.782
742
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.782
743
RYS001 Reye Syndrome 49 0.782
744
c ATM011 Autoimmune Hepatitis 63 0.782
745
TTH006 Tooth Disease 51 0.782
746
P RSP003 Respiratory Failure 74 0.782
747
GRD001 Giardiasis 46 0.782
748
ESP002 Esophageal Varix 51 0.782
749
TRC008 Trachoma 53 0.782
750
RCT015 Reactive Arthritis 61 0.782
751
P INT068 Intestinal Disease 53 0.782
752
P THY023 Thymoma 64 0.782
753
ALL009 Allergic Conjunctivitis 51 0.782
754
P BNC003 Bone Cancer 58 0.782
755
SPN027 Spinal Stenosis 59 0.782
756
HNS001 Hansen's Disease 32 0.782
757
DYS073 Dysphagia 53 0.782
758
CRV045 Cervical Intraepithelial Neoplasia 39 0.782
759
P HRD217 Hereditary Optic Neuropathy 36 0.700
760
P RTT002 Rett Syndrome 79 0.700
761
c GLL024 Gallbladder Disease 1 52 0.700
762
P CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 48 0.700
763
EPD002 Epidermolytic Hyperkeratosis 56 0.700
764
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.700
765
ARG007 Argininemia 58 0.700
766
P FTL069 Fetal Akinesia Deformation Sequence 1 63 0.700
767
HYD038 Hydrops Fetalis, Nonimmune 59 0.700
768
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.700
770
FML037 Female Breast Cancer 51 0.700
771
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 0.700
772
c GLC112 Galactosemia Iii 51 0.700
773
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.700
774
CHD004 Chudley-Mccullough Syndrome 48 0.700
775
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.700
776
P NJM001 Nijmegen Breakage Syndrome 76 0.700
777
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.700
778
HYP114 Hypertensive Nephropathy 36 0.700
779
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.700
780
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.700
781
TST044 Testicular Torsion 45 0.700
782
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.700
783
MNN043 Meningioma, Familial 79 0.700
784
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.700
785
PMP014 Pemphigoid 51 0.700
786
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.700
787
MCR004 Macroglobulinemia 49 0.700
788
CHC001 Chickenpox 57 0.700
789
GST010 Gestational Trophoblastic Neoplasm 52 0.700
790
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 0.700
791
P PLM034 Pulmonary Emphysema 58 0.700
792
MNG007 Manganese Poisoning 28 0.700
793
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 0.700
794
PLC005 Placental Insufficiency 56 0.700
795
SCR001 Secretory Meningioma 40 0.700
796
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.700
797
PRP016 Paraplegia 52 0.700
798
FBR047 Fibromyalgia 58 0.700
799
SCB001 Scabies 50 0.700
800
PYR009 Pyridoxine Deficiency Anemia 35 0.700
801
RDC002 Radiculopathy 52 0.700
802
BLL006 Bullous Pemphigoid 61 0.700
803
ALC010 Alcoholic Cardiomyopathy 42 0.700
804
CRT017 Cartilage Disease 53 0.700
805
CRY005 Cryptococcosis 60 0.700
806
VRC001 Varicocele 48 0.700
807
PPL022 Papilloma 53 0.700
808
CRY003 Cryptosporidiosis 56 0.700
809
P GLY013 Glycogen Storage Disease 60 0.700
810
ORN001 Ornithosis 39 0.700
811
P PYL005 Pyelonephritis 57 0.700
812
THY030 Thyroid Gland Disease 50 0.700
813
NRD001 Neurodermatitis 39 0.700
814
c CNT035 Central Nervous System Disease 54 0.700
815
P PTS002 Ptosis 52 0.700
816
PLS007 Plasmodium Falciparum Malaria 52 0.700
817
SPN021 Spinal Meningioma 50 0.700
818
CYS008 Cystic Echinococcosis 57 0.700
819
QDR001 Quadriplegia 50 0.700
820
VSC002 Vascular Dementia 60 0.700
821
P CHR345 Chronic Pain 50 0.700
822
P CRB059 Cerebellar Degeneration 36 0.700
823
PSD088 Pseudobulbar Affect 33 0.700
824
ADN009 Adenosquamous Carcinoma 48 0.644
825
SPN050 Spinocerebellar Degeneration 39 0.606
826
c BCT007 Bacterial Meningitis 55 0.606
827
MTH047 Methanol Poisoning 37 0.606
828
CYN003 Cyanide Poisoning 22 0.606
829
GNT167 Genetic Obesity 30 0.606
830
PFF001 Pfeiffer Syndrome 77 0.606
831
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.606
832
c DWL002 Dowling-Degos Disease 1 58 0.606
834
PSR001 Psoriatic Arthritis 62 0.606
835
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.606
836
ABT001 Abetalipoproteinemia 68 0.606
837
OTT002 Otitis Media 71 0.606
838
DGL002 D-Glyceric Aciduria 41 0.606
839
c CNG223 Congenital Methemoglobinemia 39 0.606
840
ADR016 Adrenal Cortical Carcinoma 62 0.606
841
P ADL017 Adult T-Cell Leukemia 56 0.606
843
P FML011 Familial Adenomatous Polyposis 71 0.606
844
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.606
845
P FTL001 Fetal Alcohol Syndrome 55 0.606
846
LMB024 Limbic Encephalitis 43 0.606
847
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 0.606
848
P CRP001 Carpal Tunnel Syndrome 66 0.606
849
P MCR129 Microvascular Complications of Diabetes 1 68 0.606
850
c MYC055 Mycobacterium Tuberculosis 3 15 0.606
851
HMM004 Hamamy Syndrome 39 0.606
852
P ASP006 Aspergillosis 72 0.606
853
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 47 0.606
854
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.606
855
c HYP597 Hyperprolinemia, Type Ii 43 0.606
856
RCH002 Richards-Rundle Syndrome 31 0.606
857
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 46 0.606
858
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.606
859
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.606
860
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.606
861
TNG009 Tongue Squamous Cell Carcinoma 43 0.606
862
ASB001 Asbestosis 47 0.606
863
FSC002 Fascioliasis 44 0.606
864
SCR011 Scrapie 39 0.606
865
VLK001 Volkmann Contracture 23 0.606
866
P ART018 Aortic Valve Insufficiency 52 0.606
867
P LCH002 Lichen Planus 54 0.606
868
RSC001 Rosacea 55 0.606
869
P VSC011 Vasculitis 61 0.606
870
VRL011 Viral Infectious Disease 61 0.606
871
PYD001 Pyoderma Gangrenosum 53 0.606
872
ACT162 Acute Sensory Ataxic Neuropathy 24 0.606
873
ASB003 Asbestos Intoxication 32 0.606
874
P MTH008 Methylmalonic Acidemia 52 0.606
875
ADR004 Adrenal Cortical Adenocarcinoma 38 0.606
876
TRC003 Trichomoniasis 53 0.606
877
TRT001 Teratocarcinoma 42 0.606
878
PYD002 Pyoderma 50 0.606
879
GLC008 Glucose Metabolism Disease 40 0.606
880
P ART023 Arthropathy 61 0.606
881
ACQ007 Acquired Immunodeficiency Syndrome 59 0.606
882
P BNG002 Benign Meningioma 36 0.606
883
P KRT007 Keratoconus 50 0.606
884
c MCR112 Microvascular Complications of Diabetes 2 42 0.606
885
SLD003 Sialadenitis 48 0.606
886
PLC002 Plica Syndrome 35 0.606
887
CRN017 Coronary Thrombosis 46 0.606
888
PCD001 Pica Disease 38 0.606
889
P SPN046 Spinal Muscular Atrophy 63 0.606
890
P FCL005 Focal Segmental Glomerulosclerosis 57 0.606
891
SQM002 Squamous Cell Papilloma 46 0.606
892
VST003 Vestibular Nystagmus 25 0.606
893
P NPH012 Nephrotic Syndrome 60 0.606
894
PPL002 Papillary Carcinoma 46 0.606
895
CCC001 Coccidioidomycosis 58 0.606
896
P HYD006 Hydrocephalus 61 0.606
897
MST005 Mastitis 53 0.606
898
PRT038 Protein-Energy Malnutrition 53 0.606
899
P SLP005 Sleep Disorder 61 0.606
900
CRB025 Carbohydrate Metabolic Disorder 40 0.606
901
SYN007 Synovitis 55 0.606
902
P THR015 Thrombophilia 51 0.606
903
P PRM018 Primary Hypertrophic Osteoarthropathy 56 0.606
904
GNR004 Generalized Anxiety Disorder 55 0.606
905
KRT008 Keratopathy 46 0.606
906
HYP080 Hypogonadism 50 0.606
907
HLL004 Hellp Syndrome 53 0.606
908
SNL007 Senile Cataract 40 0.606
909
P INS002 in Situ Carcinoma 53 0.606
910
P TXP001 Toxoplasmosis 60 0.606
911
P HYP263 Hypersomnia 41 0.606
912
MCR225 Macrophage Activation Syndrome 45 0.606
913
c ATM075 Autoimmune Encephalitis 40 0.606
914
ERY069 Erythrokeratoderma ''en Cocardes'' 27 0.606
915
MYC015 Mycobacterium Fortuitum 28 0.606
916
PRN019 Perinatal Necrotizing Enterocolitis 60 0.606
917
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.586
918
BWN001 Bowen-Conradi Syndrome 53 0.586
919
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 41 0.586
920
ACR041 Acromelic Frontonasal Dysostosis 53 0.586
921
VTR016 Vater/vacterl Association 49 0.586
922
P ANR048 Aniridia 1 64 0.586
923
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.586
924
NTR005 Nutritional Deficiency Disease 61 0.586
925
END040 Endogenous Depression 55 0.586
926
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.586
927
NRT001 Neurotic Disorder 56 0.586
928
VCT001 Vacterl Association 47 0.586
929
FRC013 Fructose Utilization 15 0.495
930
P DBT005 Diabetes Insipidus 54 0.495
931
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.495
932
ACT248 Acute Monoblastic/monocytic Leukemia 26 0.495
933
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.495
934
ETH012 Ethylene Glycol Poisoning 29 0.495
935
ACT228 Acute Radiation Syndrome 30 0.495
936
SDD008 Sudden Sensorineural Hearing Loss 41 0.495
937
DRV001 Dravet Syndrome 69 0.495
938
SPP011 Suppression of Tumorigenicity 12 61 0.495
939
HSD004 Hsd10 Mitochondrial Disease 45 0.495
940
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 0.495
941
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.495
942
CKS001 Ck Syndrome 40 0.495
943
MND023 Mend Syndrome 49 0.495
944
LYM007 Lymphangioleiomyomatosis 68 0.495
945
SPP012 Suppressor of Tumorigenicity 11 19 0.495
946
ENC055 Encephalopathy, Ethylmalonic 51 0.495
947
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.495
948
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.495
949
MRF001 Marfan Syndrome 76 0.495
950
MTN003 Motion Sickness 51 0.495
951
CRT072 Creutzfeldt-Jakob Disease 68 0.495
952
GLL008 Gilles De La Tourette Syndrome 65 0.495
953
GST092 Gastroesophageal Reflux 61 0.495
954