Search results for NAD

1525 hits were found for NAD

# Family MCID Name MIFTS Score
1
NTR027 Neutrophil Actin Dysfunction 27 15.288
2
P VRT014 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 24 14.410
3
CNG532 Congenital Vertebral-Cardiac-Renal Anomalies Syndrome 19 13.417
4
c VRT017 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 24 13.151
5
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 20 10.768
6
P ENC069 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 1 25 10.299
7
ENC066 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 2 25 9.757
8
P HYP769 Hyperlysinemia, Type I 42 9.372
9
AGN016 Aging 53 6.549
10
DPH001 Diphtheria 59 4.962
11
PRT037 Pertussis 49 4.779
12
CHL014 Cholera 62 4.167
13
FTT001 Fatty Liver Disease 61 3.869
14
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.511
15
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.470
16
ISC004 Ischemia 61 3.293
17
HMP009 Haemophilus Influenzae 41 3.159
18
HYP266 Hypoxia 56 3.145
19
HYP066 Hyperglycemia 60 3.126
20
c MCR133 Microvascular Complications of Diabetes 4 41 2.914
21
c MCR113 Microvascular Complications of Diabetes 3 52 2.914
22
c MCR130 Microvascular Complications of Diabetes 6 41 2.914
23
c MCR120 Microvascular Complications of Diabetes 7 47 2.914
24
P MYC084 Mycobacterium Tuberculosis 1 68 2.824
25
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.789
26
WLL004 Wallerian Degeneration 38 2.765
27
BRN071 Brain Injury 50 2.750
28
HLX001 Helix Syndrome 47 2.701
29
P MYP004 Myopathy 67 2.680
30
ANX004 Anoxia 40 2.551
31
c HYP836 Hypercholesterolemia, Familial, 1 73 2.463
32
P VSC007 Vascular Disease 62 2.385
33
P PNC035 Pancreatic Cancer 87 2.375
34
P MTC069 Mitochondrial Disorders 57 2.359
35
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.358
36
P HNT016 Huntington Disease 73 2.349
37
P ALZ034 Alzheimer Disease 87 2.324
38
CRB004 Cerebral Artery Occlusion 45 2.299
39
ART002 Arts Syndrome 66 2.295
40
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.283
41
P MTC133 Mitochondrial Myopathy 51 2.261
42
TRM010 Traumatic Brain Injury 50 2.245
43
PRM329 Premature Aging 36 2.194
44
P LNG032 Lung Cancer 98 2.189
45
ATH013 Atherosclerosis Susceptibility 63 2.188
46
GLB002 Glioblastoma 67 2.182
47
P PRP019 Peripheral Nervous System Disease 57 2.172
48
P LVR013 Liver Disease 68 2.149
49
P NRB001 Neuroblastoma 66 2.134
50
P LTR001 Lateral Sclerosis 57 2.117
51
ALL014 Allergic Encephalomyelitis 34 2.108
52
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.094
53
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 2.009
54
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.003
55
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.003
56
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.003
57
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.003
58
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.003
59
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.003
60
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.003
61
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.003
62
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.003
63
P BRS047 Breast Cancer 97 1.976
64
HPT022 Hepatoblastoma 54 1.949
65
GLM045 Glioma 62 1.949
66
CYT002 Cytokine Deficiency 43 1.949
67
GLL048 Glial Tumor 51 1.944
68
P MSC005 Muscular Dystrophy 66 1.936
69
P LKM062 Leukemia, Acute Lymphoblastic 69 1.906
70
P RTN016 Retinal Degeneration 52 1.897
71
47X002 47,xyy 47 1.888
72
LPD008 Lipid Metabolism Disorder 61 1.887
73
P NRP001 Neuropathy 59 1.870
74
c SML038 Small Cell Cancer of the Lung 68 1.830
75
P CCK001 Cockayne Syndrome 67 1.828
76
CNG034 Congestive Heart Failure 69 1.820
77
P PRK039 Parkinsonism 55 1.818
78
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.805
79
c LKM061 Leukemia, Acute Myeloid 83 1.792
80
P LNG064 Lung Cancer Susceptibility 3 69 1.792
81
P SKN015 Skin Carcinoma 71 1.781
82
MYL069 Myeloma, Multiple 76 1.765
83
GLC003 Glucose Intolerance 53 1.749
84
P PRK057 Parkinson Disease, Late-Onset 79 1.727
85
c MCR115 Microvascular Complications of Diabetes 5 65 1.723
86
P LKM002 Leukemia 65 1.722
87
CND006 Candida Glabrata 29 1.715
88
P PLM036 Pulmonary Fibrosis 65 1.712
89
P PRS040 Prostate Cancer 95 1.697
90
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.677
91
P ATX030 Ataxia-Telangiectasia 80 1.676
92
TLN003 Telangiectasis 51 1.676
93
MLD018 Mild Cognitive Impairment 48 1.674
94
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.674
95
c ACT071 Acute Kidney Failure 60 1.668
96
MTC005 Mitochondrial Metabolism Disease 44 1.637
97
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.626
98
P PLL002 Pellagra 46 1.626
99
TXC005 Toxic Shock Syndrome 61 1.624
100
P OVR042 Ovarian Cancer 88 1.593
101
P MLN008 Melanoma 75 1.559
102
PHR003 Pharyngitis 57 1.556
103
c TYP008 Type 1 Diabetes Mellitus 77 1.551
104
PRT251 Proteinuria, Chronic Benign 58 1.547
105
P LKM071 Leukemia, Chronic Lymphocytic 74 1.541
106
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.530
107
c TYP009 Type 2 Diabetes Mellitus 91 1.529
108
P GST053 Gastric Cancer 82 1.521
109
c ATR087 Atrial Standstill 1 74 1.509
110
P KLZ004 Kala-Azar 1 41 1.491
111
LSH001 Leishmaniasis 63 1.491
112
P BLD134 Bladder Cancer 79 1.490
113
ESP021 Esophageal Cancer 84 1.488
114
ART140 Arteries, Anomalies of 52 1.471
115
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.465
116
LPP008 Lipoprotein Quantitative Trait Locus 65 1.464
117
P LCT001 Lactic Acidosis 50 1.442
118
24D001 2,4-Dienoyl-Coa Reductase Deficiency 35 1.436
119
BRK010 Burkitt Lymphoma 65 1.429
120
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.429
121
OST159 Osteogenic Sarcoma 66 1.428
122
HGH043 High Grade Glioma 46 1.420
123
END057 Endometrial Cancer 76 1.410
124
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.400
125
HRW001 Hair Whorl 35 1.398
126
P HPT023 Hepatocellular Carcinoma 95 1.394
127
P ADN016 Adenocarcinoma 63 1.382
128
CHG001 Chagas Disease 65 1.382
130
LNG031 Lung Benign Neoplasm 51 1.375
131
P FBR017 Fibrosarcoma 55 1.366
133
ATS010 Autosomal Recessive Disease 42 1.357
134
PST092 Posttransplant Acute Limbic Encephalitis 29 1.357
135
48X005 48,xyyy 39 1.353
136
MSC007 Muscle Hypertrophy 64 1.348
137
P CHR012 Chronic Granulomatous Disease 69 1.348
138
LGH007 Leigh Syndrome 70 1.340
139
INS001 Insulinoma 59 1.331
140
P PHC003 Pheochromocytoma 70 1.320
141
ADR040 Adrenal Gland Pheochromocytoma 45 1.320
142
P MSC003 Muscular Atrophy 52 1.313
143
P HML002 Hemolytic Anemia 62 1.306
144
P SPP010 Suppressor of Tumorigenicity 3 50 1.302
145
FSC004 Fasciitis 49 1.296
146
NCR007 Necrotizing Fasciitis 48 1.296
147
HYP060 Hyperinsulinism 53 1.286
148
P MYL006 Myeloid Leukemia 60 1.276
149
P BRS044 Breast Adenocarcinoma 58 1.268
150
STR077 Streptococcal Toxic-Shock Syndrome 34 1.267
151
NRX001 Neuroaxonal Dystrophy 38 1.262
152
P RTN018 Retinal Disease 53 1.260
153
P KDN018 Kidney Disease 71 1.252
154
P DBT009 Diabetes Mellitus 67 1.252
155
CLN015 Colon Adenocarcinoma 64 1.250
156
STN013 Stenotrophomonas Maltophilia Infection 26 1.250
157
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.243
158
CRV035 Cervical Cancer 72 1.239
159
CRB039 Cerebrovascular Disease 65 1.235
160
MTB004 Metabolic Acidosis 48 1.230
161
HMC014 Homocysteinemia 52 1.223
162
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.217
163
APP015 Apparent Mineralocorticoid Excess 57 1.217
164
SCH014 Schistosomiasis 56 1.217
165
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.215
166
MLR004 Malaria 77 1.208
167
c DLT002 Dilated Cardiomyopathy 79 1.203
168
P RNV001 Renovascular Hypertension 48 1.196
169
CRC021 Carcinosarcoma 62 1.190
170
P MLT020 Multiple Sclerosis 79 1.190
171
P GST044 Gastritis 55 1.180
172
P INF037 Inflammatory Bowel Disease 53 1.170
173
ATM095 Autoimmune Disease 61 1.168
174
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 1.160
175
STR067 Stroke, Ischemic 79 1.150
176
P ALC033 Alcohol Use Disorder 67 1.146
177
c HPT001 Hepatitis C 61 1.146
178
LYM019 Lymphosarcoma 46 1.143
179
P LYM118 Lymphoma 66 1.139
180
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.138
181
HDN002 Head Injury 44 1.138
182
P DMN002 Dementia 65 1.137
183
HYP056 Hypoglycemia 65 1.137
184
c HPT073 Hepatitis C Virus 70 1.131
185
LBR036 Leber Plus Disease 67 1.131
186
ACT119 Acute Promyelocytic Leukemia 62 1.126
187
P CLR023 Colorectal Cancer 100 1.123
188
KRN002 Kearns-Sayre Syndrome 62 1.120
189
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.117
190
c ACT027 Acute Pancreatitis 60 1.106
191
TRN015 Transient Cerebral Ischemia 62 1.105
192
P GLM007 Glomerulonephritis 59 1.105
193
P HYP076 Hyperthyroidism 53 1.105
194
P PLM037 Pulmonary Hypertension 69 1.098
195
ALC007 Alcohol Dependence 65 1.097
196
P BCL017 B-Cell Lymphoma 57 1.097
197
CVD001 Covid-19 59 1.094
198
CHL123 Chlamydia 58 1.090
199
PPL052 Papillomatosis, Confluent and Reticulated 34 1.081
200
c HYP595 Hypertension, Essential 84 1.081
201
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 1.081
202
CHL065 Cholangiocarcinoma 57 1.080
203
INT079 Intrahepatic Cholangiocarcinoma 51 1.080
204
c CHR684 Chronic Kidney Disease 73 1.072
205
c ACT075 Acute Myocardial Infarction 55 1.066
206
THY029 Thyroid Carcinoma 55 1.066
207
P DRM053 Dermatitis, Atopic 65 1.063
208
P PNC044 Pancreatitis 61 1.063
209
CRD132 Cardiac Conduction Defect 59 1.054
210
LNG099 Lung Disease 62 1.054
211
P SNS001 Sensorineural Hearing Loss 60 1.052
212
DBT010 Diabetic Neuropathy 54 1.047
213
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.045
214
SLP001 Sleeping Sickness 56 1.045
215
OST012 Osteoarthritis 77 1.045
216
CLT003 Colitis 63 1.035
217
c SCL052 Scleroderma, Familial Progressive 60 1.035
218
PHN003 Phenylketonuria 76 1.035
219
LMB062 Limb Ischemia 55 1.035
220
BRR014 Barrett Esophagus 66 1.035
221
P RCT021 Rectum Cancer 54 1.035
222
RTN020 Retinal Vascular Disease 45 1.035
223
DPR016 Depression 64 1.031
224
PNC129 Pancreatic Adenocarcinoma 64 1.025
225
P INF032 Infertility 60 1.025
226
LYM027 Lymphopenia 56 1.015
227
ACT098 Acute Erythroid Leukemia 55 1.015
228
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.014
229
MNT002 Mental Depression 56 1.005
230
P CRN300 Coronary Heart Disease 1 73 0.994
231
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.994
232
DNT012 Dental Caries 53 0.994
233
IMP005 Impotence 52 0.994
234
SVR004 Severe Combined Immunodeficiency 70 0.994
235
VSC003 Visceral Leishmaniasis 54 0.994
236
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.994
237
SPN186 Spinal Cord Injury 60 0.994
238
P FRD001 Friedreich Ataxia 62 0.992
239
P DRR001 Diarrhea 55 0.983
240
P NTR004 Neutropenia 62 0.983
241
P CRD246 Cardiovascular System Disease 55 0.983
242
GST040 Gastric Adenocarcinoma 66 0.983
243
P MYC008 Myocarditis 59 0.983
244
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.972
245
P ATR011 Atrial Fibrillation 66 0.971
246
c ACT073 Acute Leukemia 59 0.971
247
P PRN023 Prion Disease 60 0.971
248
c ATS007 Autism Spectrum Disorder 71 0.960
249
P PRD008 Periodontitis 63 0.949
250
c LBR019 Leber Congenital Amaurosis 9 45 0.947
251
HRN029 Hearing Loss, Noise-Induced 37 0.947
252
HYP005 Hypokalemia 55 0.947
253
DWR001 Dwarfism 44 0.947
254
HRT031 Hartnup Disorder 51 0.943
255
CRT020 Cortisone Reductase Deficiency 36 0.943
256
LCT008 Lactate Dehydrogenase Deficiency 14 0.943
257
c PRC016 Pre-Eclampsia 64 0.941
258
P ATS364 Autism 72 0.934
259
ULC004 Ulcerative Colitis 74 0.934
260
P BND020 Bone Disease 60 0.934
261
INS024 Insulin-Like Growth Factor I 77 0.926
262
LYM133 Lymphoma, Hodgkin, Classic 69 0.921
263
ALL029 Allergic Disease 61 0.909
264
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.907
265
HLC007 Helicobacter Pylori Infection 67 0.907
266
CHR005 Chorioamnionitis 50 0.907
267
CHR074 Choriocarcinoma 46 0.907
268
BRN056 Bronchopulmonary Dysplasia 57 0.907
269
P TRN020 Turner Syndrome 67 0.905
270
HMN044 Human Immunodeficiency Virus Type 1 76 0.901
271
P HRT032 Heart Disease 84 0.901
272
DSS032 Disease by Infectious Agent 55 0.892
273
P GLM040 Glioma Susceptibility 1 70 0.892
274
IRN002 Iron Metabolism Disease 56 0.892
275
END086 End Stage Renal Disease 54 0.892
276
PLY100 Polyploidy 36 0.892
277
MYL009 Myelodysplastic Syndrome 67 0.892
278
c EXD008 Exudative Vitreoretinopathy 1 71 0.892
279
P CYS018 Cystitis 58 0.892
280
P GRV001 Graves' Disease 54 0.892
281
PRS045 Prostatic Hypertrophy 53 0.892
282
GRN017 Granulocytopenia 42 0.892
283
P GLC113 Galactosemia I 65 0.883
284
SJG002 Sjogren-Larsson Syndrome 53 0.883
285
NNL006 Non-Alcoholic Steatohepatitis 54 0.883
286
PRT036 Peritonitis 65 0.883
287
ANG054 Angina Pectoris 65 0.876
288
P PLY011 Polycystic Ovary Syndrome 57 0.876
289
PRS021 Prostatic Adenoma 43 0.876
290
MSC157 Muscular Dystrophy, Duchenne Type 78 0.874
291
P MYC007 Myocardial Infarction 69 0.865
292
CNS004 Constipation 56 0.865
293
SPN035 Spindle Cell Sarcoma 51 0.865
294
SRC014 Sarcoma 64 0.865
295
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.859
296
HMT002 Hematologic Cancer 61 0.859
297
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.856
298
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.856
299
DMY004 Demyelinating Disease 50 0.856
300
P BRG001 Brugada Syndrome 69 0.846
301
c OPT053 Optic Atrophy 1 62 0.846
302
BNR002 Bone Resorption Disease 47 0.846
303
ANT024 Anthrax Disease 57 0.846
304
c SPR086 Spermatogenic Failure 3 47 0.840
305
c LNG109 Lung Cancer Susceptibility 1 26 0.840
306
AMN003 Amnestic Disorder 53 0.840
307
c MJR022 Major Affective Disorder 8 37 0.836
308
c MJR024 Major Affective Disorder 9 40 0.836
309
c PCH010 Pachyonychia Congenita 3 43 0.836
310
P BPL003 Bipolar Disorder 56 0.836
311
ART016 Aortic Aneurysm 68 0.836
312
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.826
313
MLG169 Malignant Astrocytoma 57 0.826
314
HYP014 Hyperuricemia 51 0.826
315
CHL068 Cholestasis 61 0.826
316
RCK004 Rickets 64 0.826
317
P THR014 Thrombocytopenia 66 0.826
318
P LPS004 Lupus Erythematosus 61 0.826
319
SPL018 Splenomegaly 47 0.826
320
P SCH015 Schizophrenia 74 0.820
321
PST011 Pustulosis of Palm and Sole 52 0.816
322
P PSR002 Psoriasis 63 0.816
323
NRM005 Neuromuscular Disease 62 0.805
325
HST006 Histidinemia 48 0.796
326
P HYP111 Hyperprolinemia 44 0.794
327
P ECL001 Eclampsia 52 0.794
328
ANR040 Aneurysm 60 0.794
329
OCL069 Ocular Motor Apraxia 57 0.782
330
SCK003 Sickle Cell Anemia 74 0.782
331
P HYP750 Hypertriglyceridemia, Familial 61 0.782
332
P KRN004 Kernicterus 47 0.782
333
P ICH004 Ichthyosis 56 0.782
334
P HYP086 Hypothyroidism 68 0.782
335
P URN019 Urinary Tract Infection 48 0.782
336
BLR008 Bilirubin Metabolic Disorder 57 0.771
337
NRR001 Neuroretinitis 42 0.771
338
RTN023 Retinitis 45 0.771
339
PTT037 Pituitary Tumors 44 0.771
340
ARG004 Argyria 26 0.771
341
P ANP001 Anaplastic Large Cell Lymphoma 59 0.758
342
TRY001 Trypanosomiasis 50 0.758
343
SQM006 Squamous Cell Carcinoma 59 0.758
344
KRT009 Keratosis 52 0.758
345
RTN003 Retinal Ischemia 48 0.758
346
P THL005 Thalassemia 56 0.758
347
CHR178 Chromosomal Triplication 33 0.758
348
P FML187 Familial Hypertension 34 0.758
349
HYP017 Hypophosphatemia 49 0.745
350
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.745
351
WRN001 Werner Syndrome 69 0.745
352
PRT013 Portal Hypertension 59 0.745
353
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.745
354
MTC004 Mitochondrial Encephalomyopathy 42 0.745
355
c RNG024 Ring Chromosome 8 28 0.745
356
c FNC027 Fanconi Anemia, Complementation Group a 80 0.733
357
TRD006 Tardive Dyskinesia 53 0.733
358
P MPL001 Maple Syrup Urine Disease 69 0.732
359
LSC001 Lesch-Nyhan Syndrome 62 0.732
360
URT049 Urate Oxidase, Pseudogene 24 0.732
361
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.732
362
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.732
363
P TCD001 Tic Disorder 50 0.732
364
ADN018 Adenoma 58 0.732
365
P HPT021 Hepatitis 68 0.732
366
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.732
367
P KDN017 Kidney Cancer 60 0.732
368
c HPT016 Hepatitis B 62 0.732
369
P RHN004 Rhinitis 56 0.732
370
GLS001 Gliosarcoma 63 0.732
371
P HYP061 Hypertrophic Cardiomyopathy 68 0.732
372
P UVT001 Uveitis 57 0.732
373
THL010 Thalassemia Minor 30 0.732
374
SKN016 Skin Disease 63 0.732
375
CRB090 Cerebral Hypoxia 42 0.732
376
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.732
377
ALL003 Allergic Rhinitis 66 0.718
378
c PRM108 Primary Progressive Multiple Sclerosis 51 0.718
379
ORL015 Oral Squamous Cell Carcinoma 43 0.718
380
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.718
381
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.718
382
P HYP733 Hypercalciuria, Absorptive, 2 45 0.718
383
GST023 Gastric Ulcer 52 0.718
384
PLR005 Pleuropneumonia 33 0.718
385
P ATR005 Atrophic Gastritis 50 0.718
386
NRM022 Neurometabolic Disease 24 0.718
387
P XNT004 Xanthinuria 38 0.703
388
CRD223 Cardiac Arrhythmia 63 0.703
389
HMN047 Human Cytomegalovirus Infection 59 0.703
390
VCC001 Vaccinia 49 0.703
391
PTH003 Pathologic Nystagmus 52 0.703
392
c HRD142 Hereditary Xanthinuria 44 0.703
393
P AMY004 Amyloidosis 69 0.703
395
PRQ002 Paraquat Poisoning 28 0.703
396
c LNG048 Long Qt Syndrome 3 52 0.687
397
GLB001 Gilbert Syndrome 53 0.687
398
MNT001 Mantle Cell Lymphoma 65 0.687
399
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.687
400
P ART021 Arteriosclerosis 53 0.687
401
P LNG028 Long Qt Syndrome 63 0.687
402
c BSL007 Basal Cell Carcinoma 67 0.687
403
MST004 Mast Cell Neoplasm 41 0.687
404
P CTS001 Cutis Laxa 64 0.687
405
MDD018 Middle East Respiratory Syndrome 44 0.687
406
P CRN026 Corneal Edema 42 0.687
407
DRM006 Dermatitis 61 0.687
408
EXT007 Extracutaneous Mastocytoma 38 0.687
409
P SBS003 Substance Abuse 54 0.687
410
MSL001 Measles 61 0.687
411
c FML191 Familial Long Qt Syndrome 54 0.687
412
P GRF003 Graft-Versus-Host Disease 71 0.670
413
PRS129 Prostatic Hyperplasia, Benign 48 0.670
414
c SVR003 Severe Congenital Neutropenia 59 0.670
415
QFV001 Q Fever 61 0.670
416
P RHB003 Rhabdomyosarcoma 66 0.670
417
DYS015 Dysentery 49 0.670
418
c SVR005 Severe Pre-Eclampsia 49 0.670
419
P MNN013 Meningitis 65 0.670
420
P CHN012 Chondrosarcoma 56 0.651
421
P MYS005 Myositis 55 0.651
422
LYM040 Lymphoblastic Lymphoma 53 0.651
423
QLT016 Qualitative or Quantitative Defects of Protein Involved in O-Glycosylation of Alpha-Dystroglycan 6 0.651
424
P DYS007 Dyskeratosis Congenita 66 0.651
425
PLM001 Pulmonary Tuberculosis 69 0.651
426
MLT006 Multidrug-Resistant Tuberculosis 47 0.651
427
CHL061 Childhood Leukemia 47 0.651
428
P RBL001 Rubella 58 0.651
429
END085 Endometrial Serous Adenocarcinoma 43 0.651
430
INT007 Intermediate Coronary Syndrome 53 0.651
432
c ACT135 Acute Graft Versus Host Disease 51 0.651
433
PNM013 Pneumococcal Meningitis 43 0.651
434
PRM317 Primary Qualitative or Quantitative Defects of Alpha-Dystroglycan 8 0.651
435
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.651
436
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.651
437
ADN009 Adenosquamous Carcinoma 49 0.646
438
CHD001 Chediak-Higashi Syndrome 66 0.631
439
c CCK008 Cockayne Syndrome a 59 0.631
440
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 31 0.631
442
P ADV001 Advanced Sleep Phase Syndrome 41 0.631
443
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.631
444
P ALB003 Albinism-Deafness Syndrome 33 0.631
445
c LKM055 Leukemia, Acute Lymphoblastic 2 18 0.631
446
INC002 Inclusion Body Myositis 56 0.631
447
ASP030 Aspirin Resistance 41 0.631
448
CHK001 Chikungunya 60 0.631
449
P MMP001 Mumps 56 0.631
450
CLR109 Colorectal Adenocarcinoma 50 0.631
451
NPH009 Nephrolithiasis 54 0.631
452
c VRL010 Viral Hepatitis 52 0.631
453
P OBS001 Obstructive Jaundice 49 0.631
454
AML001 Amelanotic Melanoma 37 0.631
455
INT066 Interstitial Lung Disease 60 0.631
456
ALC005 Alcoholic Pancreatitis 38 0.631
457
GTR002 Goiter 52 0.631
458
P HML001 Hemolytic-Uremic Syndrome 52 0.631
459
CRD016 Cardiac Rupture 34 0.631
460
P APL001 Aplastic Anemia 72 0.607
461
P PRG013 Paraganglioma 57 0.607
462
RTN017 Retinal Detachment 60 0.607
463
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.607
464
P PLY006 Polydactyly 58 0.607
465
SRC027 Sarcoma, Synovial 58 0.607
466
CHR100 Chronic Ulcer of Skin 57 0.607
467
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.607
469
ONC002 Onchocerciasis 50 0.607
470
CLR108 Colorectal Adenoma 63 0.607
471
CRV040 Cervix Carcinoma 50 0.607
472
MCR013 Microphthalmia 59 0.607
473
CHR073 Choreatic Disease 53 0.607
474
DNG003 Dengue Disease 65 0.607
475
P CWD010 Cowden Syndrome 70 0.607
476
P HMC002 Homocystinuria 52 0.607
477
IMP004 Impetigo 48 0.607
478
ATN004 Autonomic Neuropathy 42 0.597
479
WHP002 Whiplash 35 0.591
480
ALC006 Alcoholic Hepatitis 61 0.582
481
WLK001 Walker-Warburg Syndrome 62 0.580
482
PLY150 Polykaryocytosis Inducer 29 0.580
483
CRC014 Carcinoid Tumors, Intestinal 46 0.580
484
c ACT004 Acute Diarrhea 40 0.580
485
c PNC106 Pancreatic Agenesis 1 51 0.580
487
THY111 Thyroid Carcinoma, Familial Medullary 67 0.580
488
c SPN294 Spinocerebellar Ataxia 1 53 0.580
489
c CCK007 Cockayne Syndrome B 56 0.580
490
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.580
491
PRS119 Persistent Genital Arousal Disorder 18 0.580
492
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.580
493
HMR023 Hemorrhagic Cystitis 43 0.580
494
ANT019 Anterograde Amnesia 38 0.580
495
P INT143 Interstitial Cystitis 59 0.580
496
P MYP006 Myopia 55 0.580
497
P ESP024 Esophagitis 60 0.580
498
PNC034 Pancreas Disease 49 0.580
499
EXS001 Exostosis 49 0.580
500
ENT004 Enthesopathy 51 0.580
501
THY125 Thyroid Gland Medullary Carcinoma 48 0.580
502
PRM236 Primary Biliary Cholangitis 62 0.580
503
TXC004 Toxic Diffuse Goiter 24 0.580
504
P NRF002 Neurofibromatosis 60 0.580
505
SKN019 Skin Melanoma 70 0.580
506
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.580
507
PPT005 Peptic Ulcer Disease 58 0.580
508
ACR006 Aceruloplasminemia 63 0.578
509
VTR016 Vater/vacterl Association 50 0.578
510
P ANR048 Aniridia 1 66 0.578
511
ACR041 Acromelic Frontonasal Dysostosis 53 0.578
512
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.578
513
BWN001 Bowen-Conradi Syndrome 54 0.578
514
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 40 0.578
515
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.578
516
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.578
517
P ATX024 Ataxia-Oculomotor Apraxia 3 46 0.578
518
LNG116 Long Covid 21 0.578
519
END040 Endogenous Depression 54 0.578
520
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.578
521
NRT001 Neurotic Disorder 56 0.578
522
NTR005 Nutritional Deficiency Disease 60 0.578
523
VCT001 Vacterl Association 46 0.578
524
P ENC018 Encephalopathy 62 0.544
525
DGT002 Digital Clubbing, Isolated Congenital 26 0.544
526
TLC001 Telecanthus 34 0.544
527
PPL035 Papillary Thyroid Microcarcinoma 39 0.544
528
c MCR245 Microphthalmia, Syndromic 8 46 0.544
529
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.544
531
PRK088 Parkinson Disease, Mitochondrial 19 0.544
532
P BLD062 Bile Duct Cancer 69 0.544
533
ACR014 Acral Lentiginous Melanoma 53 0.544
534
IGG001 Iga Glomerulonephritis 50 0.544
535
PLM031 Poliomyelitis 62 0.544
536
CRN030 Coronary Stenosis 50 0.544
537
TRN007 Transsexualism 38 0.544
538
END062 Endometrial Hyperplasia 47 0.544
539
RHM001 Rheumatic Fever 59 0.544
540
MYL078 Myelodysplastic Syndrome with Single Lineage Dysplasia 11 0.544
541
RFR010 Refractory Anemia 49 0.544
542
P SCK005 Sickle Cell Disease 56 0.530
543
BRN004 Brain Edema 54 0.477
544
P ADL010 Adult Respiratory Distress Syndrome 70 0.461
545
RTC009 Reticulum Cell Sarcoma 43 0.456
546
SCT005 Scott Syndrome 51 0.456
547
SPN450 Spondyloepiphyseal Dysplasia, Sensorineural Hearing Loss, Impaired Intellectual Development, and Leber Congenital Amaurosis 17 0.456
548
c LCT020 Lactic Acidosis, Chronic Adult Form 8 0.456
549
LGN006 Legionnaire Disease 52 0.456
550
TLR001 Tularemia 56 0.456
551
IMM001 Immune-Complex Glomerulonephritis 36 0.456
552
MMB001 Membranoproliferative Glomerulonephritis 56 0.456
553
PNC013 Pancreatic Ductal Carcinoma 48 0.456
554
CRN027 Corneal Neovascularization 47 0.456
555
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.453
556
STT001 Status Epilepticus 58 0.453
557
RNL077 Renal Fibrosis 46 0.444
558
DBT002 Diabetic Autonomic Neuropathy 40 0.436
559
ANX010 Anxiety 70 0.427
560
P MJR001 Major Depressive Disorder 68 0.427
561
P SZR006 Seizure Disorder 69 0.409
562
P DYS154 Dystonia 64 0.399
563
BCT022 Bacterial Infectious Disease 55 0.390
564
P MTH007 Methemoglobinemia 46 0.390
565
LNG108 Langerhans Cell Histiocytosis 57 0.380
566
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.380
567
HST010 Histiocytosis 49 0.380
568
P OPT006 Optic Nerve Disease 57 0.380
569
ART074 Aortic Dissection 53 0.370
570
P EPL164 Epilepsy 70 0.370
571
P CTR002 Cataract 59 0.370
572
P CRD119 Cardiac Arrest 68 0.359
573
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.359
574
PSY004 Psychotic Disorder 66 0.359
575
ECH003 Echinococcosis 52 0.359
576
P ART022 Arthritis 70 0.359
577
P TRM003 Tremor 50 0.359
578
CTR172 Citrullinemia, Classic 64 0.348
579
ENT011 Enterocolitis 55 0.348
580
LVR012 Liver Cirrhosis 62 0.348
581
URT010 Ureteral Obstruction 44 0.348
582
P EYD002 Eye Disease 57 0.348
583
P PLY019 Polyneuropathy 52 0.348
584
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.337
585
HYP025 Hyperphosphatemia 47 0.337
586
HPT004 Hepatic Coma 43 0.337
587
c INH020 Inherited Metabolic Disorder 47 0.337
588
BRN024 Bronchitis 67 0.337
589
STM007 Stomatitis 52 0.337
590
DWN001 Down Syndrome 70 0.326
591
P RTN024 Retinoblastoma 72 0.326
592
HPT019 Hepatic Encephalopathy 59 0.326
593
P MTR014 Motor Neuron Disease 65 0.326
594
SPS057 Spasticity 43 0.326
595
ASP007 Aspiration Pneumonia 49 0.314
596
c SYS001 Systemic Lupus Erythematosus 85 0.314
597
P RTN008 Retinitis Pigmentosa 79 0.314
598
HRY003 Hairy Cell Leukemia 53 0.314
599
HMS001 Hemosiderosis 48 0.314
600
P CND004 Candidiasis 57 0.314
601
PLR008 Pleurisy 49 0.314
602
P HRS035 Hirschsprung Disease 1 66 0.302
603
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.302
604
RBF001 Riboflavin Deficiency 49 0.302
605
P TMP001 Temporal Lobe Epilepsy 49 0.302
606
P ACN011 Acne 55 0.302
607
PLM010 Pulmonary Edema 54 0.302
608
CRT015 Carotid Artery Occlusion 45 0.302
609
TTR011 Tetraploidy 43 0.302
610
P RHM011 Rheumatoid Arthritis 81 0.289
611
c LKM063 Leukemia, Chronic Myeloid 70 0.289
612
THR024 Thrombosis 56 0.289
613
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.289
614
P RNL015 Renal Hypertension 45 0.289
615
TTN003 Tetanus 64 0.289
616
P ENC004 Encephalitis 61 0.289
617
P HRP006 Herpes Simplex 65 0.289
618
P RRH023 Rare Hereditary Hemochromatosis 52 0.289
619
EPL131 Epilepsy, Pyridoxine-Dependent 46 0.275
620
EWN003 Ewing Sarcoma 69 0.275
621
GST045 Gastroenteritis 58 0.275
622
URM002 Uremia 47 0.275
623
GT001 Gout 63 0.275
624
CHR066 Chronic Fatigue Syndrome 59 0.275
625
ATN005 Autonomic Dysfunction 45 0.275
626
P HYP265 Hypotonia 42 0.275
627
DFC004 Deficiency Anemia 74 0.261
628
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.261
629
ADR007 Adrenoleukodystrophy 73 0.261
630
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.261
631
IMM167 Immune Deficiency Disease 76 0.261
632
P WSK001 Wiskott-Aldrich Syndrome 72 0.261
633
FRN006 Frontotemporal Dementia 68 0.261
634
P AST005 Asthma 75 0.261
635
GNG005 Gangliocytoma 54 0.261
636
c HRD010 Hereditary Spastic Paraplegia 65 0.261
637
GNG002 Ganglioneuroma 52 0.261
638
P CNJ013 Conjunctivitis 66 0.261
639
SVR001 Severe Acute Respiratory Syndrome 68 0.261
640
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.261
641
LST001 Listeriosis 59 0.261
642
P MCR010 Microcephaly 59 0.261
643
ALV002 Alveolar Echinococcosis 56 0.261
644
ADR022 Adrenomyeloneuropathy 38 0.261
645
P INF038 Influenza 68 0.261
646
GLM044 Glomerular Disease 34 0.261
647
c RNG015 Ring Chromosome 2 22 0.261
648
c ACT134 Acute Liver Failure 57 0.261
649
APR001 Apraxia 51 0.246
650
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.246
651
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.246
652
RFS006 Refsum Disease, Classic 63 0.246
653
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.246
654
P NSP012 Nasopharyngeal Carcinoma 60 0.246
655
MTH071 Methane Production 24 0.246
656
P STR020 Strabismus 56 0.246
657
P MLN007 Male Infertility 56 0.246
658
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.246
659
OVR063 Overnutrition 42 0.246
660
P END044 Endometriosis 62 0.246
661
MDD011 Mood Disorder 61 0.246
662
LKS001 Leukostasis 40 0.246
663
c JVN010 Juvenile Rheumatoid Arthritis 52 0.246
664
ALL006 Allergic Asthma 55 0.246
665
PRX001 Peroxisomal Disease 46 0.246
666
MCH006 Mechanical Strabismus 40 0.246
667
P NRV007 Nervous System Disease 65 0.246
668
P HYP098 Hypereosinophilic Syndrome 66 0.246
669
ATX019 Ataxia with Vitamin E Deficiency 44 0.246
670
ORL011 Oral Cancer 60 0.246
671
CRT033 Corticobasal Degeneration 48 0.246
672
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.230
673
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.230
674
P CTN015 Cutaneous T Cell Lymphoma 48 0.230
675
PNG002 Pain Agnosia 51 0.230
676
OBS002 Obsessive-Compulsive Disorder 67 0.230
677
P OST002 Osteoporosis 76 0.230
678
c SPN291 Spinocerebellar Ataxia 7 50 0.230
679
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.230
680
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.230
681
KPS004 Kaposi Sarcoma 76 0.230
682
P MYS003 Myasthenia Gravis 67 0.230
683
c THY071 Thyroid Dyshormonogenesis 1 31 0.230
684
P PLY014 Polycystic Kidney Disease 71 0.230
685
c CHR418 Chronic Leukemia 48 0.230
686
FCL014 Focal Epilepsy 53 0.230
687
PRP030 Purpura 54 0.230
688
P PRM002 Primary Hyperoxaluria 65 0.230
689
DBT007 Diabetic Cataract 36 0.230
690
URN010 Urinary Tract Obstruction 55 0.230
691
LYM017 Lyme Disease 63 0.230
692
HPT014 Hepatorenal Syndrome 49 0.230
693
ART004 Aortic Atherosclerosis 46 0.230
694
SPS003 Spastic Diplegia 52 0.230
695
P ZLL001 Zellweger Syndrome 65 0.230
696
CHL045 Choline Deficiency Disease 39 0.230
697
HML018 Homologous Wasting Disease 21 0.230
698
OVR094 Ovarian Epithelial Cancer 39 0.230
699
IRR002 Irritable Bowel Syndrome 64 0.230
700
MYT011 Myotonia 37 0.230
701
SPS019 Spastic Paraparesis 38 0.230
702
ORG002 Organic Acidemia 43 0.213
703
CYS001 Cystic Fibrosis 77 0.213
704
PHS027 Phosphoglycoprotein 1 14 0.213
705
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 63 0.213
706
P TRT019 Torticollis 47 0.213
707
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.213
708
c THY056 Thyroid Dyshormonogenesis 3 32 0.213
709
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.213
710
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.213
711
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.213
712
c RTN130 Retinitis Pigmentosa 46 40 0.213
713
DFF005 Diffuse Large B-Cell Lymphoma 55 0.213
714
BCT021 Bacterial Sepsis 43 0.213
715
OST003 Osteonecrosis 60 0.213
716
P BNG032 Benign Mesothelioma 53 0.213
717
NRT004 Neuritis 53 0.213
718
GST037 Gastroparesis 52 0.213
719
BRN002 Bronchiolitis 57 0.213
720
AVN001 Avian Influenza 61 0.213
721
P PSD015 Pseudohypoparathyroidism 54 0.213
722
GST033 Gestational Diabetes 60 0.213
723
c ACT068 Acute Cystitis 60 0.213
724
SCL003 Social Phobia 48 0.213
725
DBT004 Diabetic Polyneuropathy 50 0.213
726
P GLL022 Guillain-Barre Syndrome 59 0.213
727
P OPT009 Optic Neuritis 57 0.213
728
BRN028 Brain Cancer 73 0.213
729
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.213
730
CRB001 Cerebral Lymphoma 37 0.213
731
ACH005 Achalasia 54 0.213
732
ACT200 Acute Monoblastic Leukemia 40 0.213
733
P MLG056 Malignant Hyperthermia 65 0.213
734
P MNC007 Monocytic Leukemia 48 0.213
735
PST021 Postpartum Depression 50 0.213
736
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.213
737
c LKM005 Leukemia, T-Cell, Chronic 33 0.213
738
NRM001 Neuromyelitis Optica 60 0.213
739
P MTR004 Maturity-Onset Diabetes of the Young 66 0.195
740
P SLP006 Sleep Apnea 69 0.195
741
TCK001 Tick-Borne Encephalitis 58 0.195
742
VRC005 Varicose Veins 59 0.195
743
c MGR028 Migraine with or Without Aura 1 63 0.195
744
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 48 0.195
745
c BRN108 Branchiootic Syndrome 1 63 0.195
746
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.195
747
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.195
748
PRP027 Peripheral Vascular Disease 71 0.195
749
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.195
750
P EXN002 Exanthem 58 0.195
751
c THY107 Thymoma, Familial 42 0.195
752
P LPR021 Leprosy 3 71 0.195
753
PHB003 Phobia, Specific 44 0.195
754
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.195
755
P MMB011 Membranous Nephropathy 50 0.195
756
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 52 0.195
757
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.195
758
ESP002 Esophageal Varix 51 0.195
759
TRC008 Trachoma 53 0.195
760
PRP080 Peripheral Artery Disease 54 0.195
761
TTH006 Tooth Disease 51 0.195
762
SPN020 Spondylosis 46 0.195
763
c ATM011 Autoimmune Hepatitis 62 0.195
764
P THY023 Thymoma 64 0.195
765
P BNC003 Bone Cancer 58 0.195
766
P BRB001 Beriberi 44 0.195
767
RCT015 Reactive Arthritis 60 0.195
768
P INT068 Intestinal Disease 53 0.195
769
RYS001 Reye Syndrome 49 0.195
770
P CHR071 Charcot-Marie-Tooth Disease 64 0.195
771
GRD001 Giardiasis 46 0.195
772
ALL009 Allergic Conjunctivitis 51 0.195
773
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.195
774
CYS008 Cystic Echinococcosis 57 0.195
775
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.195
776
ACT003 Acute Kidney Tubular Necrosis 46 0.195
777
ADN001 Adenosine Deaminase Deficiency 59 0.195
778
P PNC025 Panic Disorder 52 0.195
779
SPN027 Spinal Stenosis 58 0.195
780
CRV002 Cervix Uteri Carcinoma in Situ 48 0.195
781
DGN001 Degenerative Disc Disease 48 0.195
782
HNS001 Hansen's Disease 32 0.195
783
BCK006 Back Pain 43 0.195
784
CRV045 Cervical Intraepithelial Neoplasia 38 0.195
785
DYS073 Dysphagia 53 0.195
786
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.174
787
P PTS002 Ptosis 52 0.174
788
P FTL069 Fetal Akinesia Deformation Sequence 1 63 0.174
789
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.174
790
HYD038 Hydrops Fetalis, Nonimmune 57 0.174
791
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.174
792
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.174
793
P NJM001 Nijmegen Breakage Syndrome 75 0.174
794
c GLC112 Galactosemia Iii 51 0.174
795
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.174
796
P RTT002 Rett Syndrome 79 0.174
797
c LYM150 Lymphatic Malformation 7 43 0.174
798
FML037 Female Breast Cancer 51 0.174
799
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 0.174
800
HYP114 Hypertensive Nephropathy 35 0.174
802
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.174
803
P CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 48 0.174
804
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.174
805
ARG007 Argininemia 58 0.174
806
TST044 Testicular Torsion 45 0.174
807
c GLL024 Gallbladder Disease 1 53 0.174
808
MNN043 Meningioma, Familial 79 0.174
809
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.174
810
EPD002 Epidermolytic Hyperkeratosis 55 0.174
811
CHD004 Chudley-Mccullough Syndrome 47 0.174
812
c NRD009 Neurodegeneration with Brain Iron Accumulation 2b 45 0.174
813
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.174
814
ORN001 Ornithosis 39 0.174
815
PPL022 Papilloma 53 0.174
816
P GLY013 Glycogen Storage Disease 59 0.174
817
P PYL005 Pyelonephritis 56 0.174
818
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.174
819
c CNT035 Central Nervous System Disease 53 0.174
820
PRP016 Paraplegia 52 0.174
821
FBR047 Fibromyalgia 57 0.174
822
SCR001 Secretory Meningioma 40 0.174
823
THY030 Thyroid Gland Disease 50 0.174
824
PLC005 Placental Insufficiency 55 0.174
825
NRD001 Neurodermatitis 39 0.174
826
GST010 Gestational Trophoblastic Neoplasm 52 0.174
827
RDC002 Radiculopathy 51 0.174
828
QDR001 Quadriplegia 49 0.174
829
PMP014 Pemphigoid 48 0.174
830
INT395 Intracranial Meningioma 47 0.174
831
CRT017 Cartilage Disease 52 0.174
832
CRY003 Cryptosporidiosis 55 0.174
833
PLS007 Plasmodium Falciparum Malaria 52 0.174
834
ALC010 Alcoholic Cardiomyopathy 42 0.174
835
CRY005 Cryptococcosis 61 0.174
836
VRC001 Varicocele 48 0.174
837
SCB001 Scabies 49 0.174
838
BLL006 Bullous Pemphigoid 61 0.174
839
MCR004 Macroglobulinemia 48 0.174
840
P PLM034 Pulmonary Emphysema 58 0.174
841
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.174
842
PYR009 Pyridoxine Deficiency Anemia 35 0.174
843
CHC001 Chickenpox 56 0.174
844
VSC002 Vascular Dementia 59 0.174
845
CRH001 Crohn's Disease 80 0.174
846
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 37 0.174
847
P CRB059 Cerebellar Degeneration 36 0.174
848
MNG007 Manganese Poisoning 28 0.174
849
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.174
850
P HRD217 Hereditary Optic Neuropathy 36 0.174
851
PSD088 Pseudobulbar Affect 33 0.174
852
P CHR345 Chronic Pain 50 0.174
853
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.151
854
HMM004 Hamamy Syndrome 39 0.151
855
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.151
856
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.151
857
PSR001 Psoriatic Arthritis 61 0.151
858
TNG009 Tongue Squamous Cell Carcinoma 43 0.151
859
PFF001 Pfeiffer Syndrome 77 0.151
860
OTT002 Otitis Media 70 0.151
861
c DWL002 Dowling-Degos Disease 1 58 0.151
863
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.151
864
P MCR129 Microvascular Complications of Diabetes 1 67 0.151
865
c CNG223 Congenital Methemoglobinemia 39 0.151
866
P FML011 Familial Adenomatous Polyposis 70 0.151
867
IFP003 Ifap Syndrome 2 41 0.151
868
c MCR112 Microvascular Complications of Diabetes 2 42 0.151
869
ADR016 Adrenal Cortical Carcinoma 61 0.151
871
ABT001 Abetalipoproteinemia 68 0.151
872
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.151
873
DGL002 D-Glyceric Aciduria 40 0.151
874
P CRP001 Carpal Tunnel Syndrome 65 0.151
875
c HYP597 Hyperprolinemia, Type Ii 43 0.151
876
RCH002 Richards-Rundle Syndrome 31 0.151
877
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.151
878
P TMR010 Tumor Predisposition Syndrome 69 0.151
879
c MYC055 Mycobacterium Tuberculosis 3 13 0.151
880
P ASP006 Aspergillosis 71 0.151
881
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.151
882
MRF001 Marfan Syndrome 76 0.151
883
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.151
884
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 47 0.151
885
P ADL017 Adult T-Cell Leukemia 53 0.151
886
P FTL001 Fetal Alcohol Syndrome 55 0.151
887
P HYP700 Hypomyelinating Leukodystrophy 35 0.151
888
P RSP003 Respiratory Failure 73 0.151
889
P NPH012 Nephrotic Syndrome 61 0.151
890
LMB024 Limbic Encephalitis 43 0.151
891
SLD003 Sialadenitis 47 0.151
892
ASB001 Asbestosis 47 0.151
893
KRT008 Keratopathy 46 0.151
894
HYP080 Hypogonadism 49 0.151
895
PPL002 Papillary Carcinoma 46 0.151
896
P THR015 Thrombophilia 51 0.151
897
CRB025 Carbohydrate Metabolic Disorder 41 0.151
898
TRC003 Trichomoniasis 53 0.151
899
CCC001 Coccidioidomycosis 57 0.151
900
P SPN046 Spinal Muscular Atrophy 62 0.151
901
VLK001 Volkmann Contracture 23 0.151
902
SQM002 Squamous Cell Papilloma 45 0.151
903
SYN007 Synovitis 54 0.151
904
P BNG002 Benign Meningioma 36 0.151
905
PYD002 Pyoderma 49 0.151
906
P ART023 Arthropathy 59 0.151
907
ADR004 Adrenal Cortical Adenocarcinoma 38 0.151
908
TRT001 Teratocarcinoma 41 0.151
909
GLC008 Glucose Metabolism Disease 40 0.151
910
PLC002 Plica Syndrome 35 0.151
911
PRT038 Protein-Energy Malnutrition 53 0.151
912
CRN017 Coronary Thrombosis 46 0.151
913
P LKD001 Leukodystrophy 58 0.151
914
MST005 Mastitis 52 0.151
915
P HYD006 Hydrocephalus 62 0.151
916
P FCL005 Focal Segmental Glomerulosclerosis 57 0.151
917
PCD001 Pica Disease 38 0.151
918
P MTH008 Methylmalonic Acidemia 52 0.151
919
VST003 Vestibular Nystagmus 25 0.151
920
GNR004 Generalized Anxiety Disorder 54 0.151
921
P PRM018 Primary Hypertrophic Osteoarthropathy 56 0.151
922
P KRT007 Keratoconus 49 0.151
923
HLL004 Hellp Syndrome 53 0.151
924
P SLP005 Sleep Disorder 61 0.151
925
SCR011 Scrapie 39 0.151
926
P ART018 Aortic Valve Insufficiency 52 0.151
927
ACQ007 Acquired Immunodeficiency Syndrome 58 0.151
928
P VSC011 Vasculitis 61 0.151
929
FSC002 Fascioliasis 43 0.151
930
RSC001 Rosacea 55 0.151
931
VRL011 Viral Infectious Disease 60 0.151
932
SNL007 Senile Cataract 40 0.151
933
P LCH002 Lichen Planus 54 0.151
934
PYD001 Pyoderma Gangrenosum 53 0.151
935
PRN019 Perinatal Necrotizing Enterocolitis 60 0.151
936
P INS002 in Situ Carcinoma 52 0.151
937
P TXP001 Toxoplasmosis 59 0.151
938
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.151
939
c BCT007 Bacterial Meningitis 55 0.151
940
ASB003 Asbestos Intoxication 32 0.151
941
MCR225 Macrophage Activation Syndrome 45 0.151
942
c ATM075 Autoimmune Encephalitis 39 0.151
943
CYN003 Cyanide Poisoning 22 0.151
944
ACT162 Acute Sensory Ataxic Neuropathy 24 0.151
945
MYC015 Mycobacterium Fortuitum 28 0.151
946
INH023 Inherited Cancer-Predisposing Syndrome 53 0.151
947
P HYP263 Hypersomnia 40 0.151
948
SPN050 Spinocerebellar Degeneration 38 0.151
949
MTH047 Methanol Poisoning 37 0.151
950
GNT167 Genetic Obesity 33 0.151
951
INF034 Infective Endocarditis 53 0.123
952
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.123
953