Search results for (neurodegenerative OR senile) AND alzheimer

2070 hits were found for (neurodegenerative OR senile) AND alzheimer

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 87 268.960
2
P DMN002 Dementia 66 103.184
3
MLD018 Mild Cognitive Impairment 48 98.430
4
c AMY091 Amyotrophic Lateral Sclerosis 1 88 73.851
5
P LTR001 Lateral Sclerosis 58 72.631
6
VSC002 Vascular Dementia 60 69.074
7
P HNT016 Huntington Disease 73 66.648
8
FRN006 Frontotemporal Dementia 68 61.723
9
AGN016 Aging 54 55.565
10
P AMY004 Amyloidosis 70 54.952
11
c ALZ049 Alzheimer Disease 2 48 54.690
12
P PRK057 Parkinson Disease, Late-Onset 80 52.585
13
c ALZ056 Alzheimer Disease 3 55 52.239
14
DMN031 Dementia, Lewy Body 65 51.796
15
P PRK039 Parkinsonism 55 50.658
16
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 49.788
17
P SPR120 Supranuclear Palsy, Progressive, 1 69 46.915
18
SNL007 Senile Cataract 40 44.535
19
DWN001 Down Syndrome 70 43.634
20
c ALZ054 Alzheimer Disease 4 43 42.542
22
P PRN023 Prion Disease 60 39.929
23
APH002 Aphasia 56 39.440
24
P NRB001 Neuroblastoma 66 38.705
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 38.477
26
CRB039 Cerebrovascular Disease 66 38.377
28
P ENC018 Encephalopathy 62 36.673
29
c ALZ045 Alzheimer Disease 9 45 35.878
30
P CTR002 Cataract 60 34.553
31
PCK003 Pick Disease of Brain 69 34.029
32
CRT072 Creutzfeldt-Jakob Disease 68 33.992
33
c ALZ057 Alzheimer Disease 10 35 33.891
34
c ALZ062 Alzheimer Disease 19 36 33.592
35
c ALZ032 Alzheimer Disease 18 34 33.357
36
c ALZ050 Alzheimer Disease 5 33 32.906
37
c ALZ015 Alzheimer Disease 6 26 32.769
38
SNL009 Senile Plaque Formation 29 32.656
39
c ALZ063 Alzheimer's Disease 1 31 32.170
40
CRT033 Corticobasal Degeneration 47 32.135
41
P OST002 Osteoporosis 76 31.930
42
P TRM003 Tremor 48 30.785
43
c ALZ058 Alzheimer Disease 11 28 30.441
44
TRM010 Traumatic Brain Injury 51 30.084
45
c ALZ016 Alzheimer Disease 8 27 30.021
46
MLT157 Multiple System Atrophy 1 69 29.965
47
BNS003 Binswanger's Disease 41 29.084
48
c ALZ012 Alzheimer Disease 12 24 29.052
49
c ALZ053 Alzheimer Disease 7 32 29.048
51
c ALZ060 Alzheimer Disease 14 21 28.494
52
PST086 Posterior Cortical Atrophy 36 27.657
53
P MTR014 Motor Neuron Disease 65 27.049
54
c ALZ031 Alzheimer Disease 17 28 26.775
55
c ALZ061 Alzheimer Disease 15 28 26.300
56
c ALZ059 Alzheimer Disease 13 26 26.245
57
P VSC007 Vascular Disease 63 25.718
58
APR001 Apraxia 52 25.168
59
AMN003 Amnestic Disorder 54 25.082
60
DPR016 Depression 65 25.037
61
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 24.812
62
P MLT020 Multiple Sclerosis 79 23.979
63
BRN071 Brain Injury 50 23.860
64
P CRB088 Cerebral Atrophy 33 23.615
65
c TYP009 Type 2 Diabetes Mellitus 92 23.443
66
INT323 Intraocular Pressure Quantitative Trait Locus 64 23.168
67
P HYD006 Hydrocephalus 61 22.620
68
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 22.592
69
WLD005 Wild Type Attr Amyloidosis 29 22.227
70
P SLP005 Sleep Disorder 61 21.742
71
SCR011 Scrapie 39 21.483
72
MNT002 Mental Depression 57 21.439
73
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 21.087
74
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 21.087
75
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 20.620
76
CHR073 Choreatic Disease 54 20.620
77
DMN026 Dementia Pugilistica 27 20.593
78
c HNT010 Huntington Disease-Like 1 55 20.533
79
P MYC033 Myoclonus 47 20.415
80
SMN008 Semantic Dementia 47 20.366
81
P NRM002 Normal Pressure Hydrocephalus 49 20.266
82
HDN002 Head Injury 44 20.227
83
ALZ029 Alzheimer Disease Mitochondrial 24 19.621
84
P MVM001 Movement Disease 61 19.541
85
SBC016 Subacute Delirium 43 19.357
86
P BPL003 Bipolar Disorder 56 19.324
87
c HYP836 Hypercholesterolemia, Familial, 1 73 19.092
88
P MSC003 Muscular Atrophy 52 19.030
89
c MJR022 Major Affective Disorder 8 38 18.736
90
c MJR024 Major Affective Disorder 9 41 18.736
91
P DBT009 Diabetes Mellitus 67 18.586
92
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 18.083
93
MDD011 Mood Disorder 62 17.872
95
CHR178 Chromosomal Triplication 34 17.190
96
P EPL164 Epilepsy 68 17.168
97
c MCR115 Microvascular Complications of Diabetes 5 65 17.044
98
KHN001 Kuhnt-Junius Degeneration 48 16.768
99
P HRP006 Herpes Simplex 65 16.719
100
HYP066 Hyperglycemia 61 16.711
101
BLL006 Bullous Pemphigoid 61 16.683
102
P PLY019 Polyneuropathy 52 16.601
103
CYT002 Cytokine Deficiency 43 16.569
104
P NRN021 Neuronal Ceroid Lipofuscinosis 65 16.554
105
P SCH015 Schizophrenia 74 16.548
106
STR067 Stroke, Ischemic 80 16.363
107
P MJR001 Major Depressive Disorder 68 16.253
108
P SLP006 Sleep Apnea 69 16.236
109
P RRN010 Rare Neurodegenerative Disease 14 16.115
110
SBJ001 Subjective Cognitive Decline 30 15.882
111
P DYS154 Dystonia 64 15.820
112
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 15.673
113
DYS073 Dysphagia 53 15.650
114
P AGN002 Agnosia 54 15.638
115
NRR001 Neuroretinitis 42 15.602
116
HMC014 Homocysteinemia 52 15.568
117
RTN023 Retinitis 46 15.469
118
CRB033 Cerebral Degeneration 39 15.450
119
RMS001 Rem Sleep Behavior Disorder 47 15.414
120
P SZR006 Seizure Disorder 70 15.328
121
ANX010 Anxiety 70 15.197
122
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 15.186
123
ARG004 Argyria 26 15.105
124
LPD008 Lipid Metabolism Disorder 62 15.083
125
c ESS001 Essential Tremor 57 15.024
126
P PHC003 Pheochromocytoma 69 15.013
127
ADR040 Adrenal Gland Pheochromocytoma 46 15.013
128
P NRP001 Neuropathy 60 14.967
129
RPD005 Rapidly Involuting Congenital Hemangioma 46 14.840
130
P OPN001 Open-Angle Glaucoma 55 14.724
131
KHL003 Kohlschutter-Tonz Syndrome 59 14.643
132
SPN186 Spinal Cord Injury 61 14.606
133
P SPN046 Spinal Muscular Atrophy 63 14.537
134
P ART021 Arteriosclerosis 54 14.527
135
P MYP004 Myopathy 67 14.364
136
HYP266 Hypoxia 57 14.333
137
c ATS007 Autism Spectrum Disorder 72 14.243
138
ATH013 Atherosclerosis Susceptibility 63 14.138
139
ISC004 Ischemia 61 13.962
140
PRP016 Paraplegia 52 13.863
141
ATM095 Autoimmune Disease 61 13.832
142
KR002 Kuru 45 13.768
143
P ENC004 Encephalitis 61 13.671
144
ALC007 Alcohol Dependence 66 13.523
145
P RTN016 Retinal Degeneration 52 13.492
146
P OPT006 Optic Nerve Disease 58 13.472
147
47X002 47,xyy 48 13.437
148
c BRN108 Branchiootic Syndrome 1 62 13.311
149
PRT058 Pure Autonomic Failure 58 13.231
150
PSY004 Psychotic Disorder 66 13.145
151
P MCH002 Machado-Joseph Disease 62 12.942
152
TLN003 Telangiectasis 51 12.919
153
P PRP019 Peripheral Nervous System Disease 58 12.893
154
P NRV007 Nervous System Disease 67 12.834
155
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 12.773
156
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 12.754
157
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 12.744
158
P TMP001 Temporal Lobe Epilepsy 49 12.734
159
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 12.731
160
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 12.731
161
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 12.731
162
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 12.731
163
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 12.731
164
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 12.731
165
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 12.731
166
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 12.731
167
GNT083 Genetic Neurodegenerative Disease 9 12.710
168
P EYD002 Eye Disease 57 12.655
169
ATN005 Autonomic Dysfunction 46 12.631
170
SPS057 Spasticity 42 12.557
171
MNN009 Meningoencephalitis 48 12.534
172
ALL014 Allergic Encephalomyelitis 34 12.513
173
ANS006 Anosognosia 34 12.439
174
P BCL017 B-Cell Lymphoma 59 12.231
175
P RRH023 Rare Hereditary Hemochromatosis 54 12.087
176
LYS002 Lysosomal Storage Disease 51 12.054
177
SPS019 Spastic Paraparesis 38 11.988
178
P ATX030 Ataxia-Telangiectasia 80 11.984
179
c CNT035 Central Nervous System Disease 54 11.887
180
HMS001 Hemosiderosis 48 11.810
181
P PRD008 Periodontitis 64 11.808
182
c GLC092 Glaucoma, Primary Open Angle 62 11.617
183
HLX001 Helix Syndrome 48 11.513
184
PRM329 Premature Aging 36 11.498
185
P LKD001 Leukodystrophy 59 11.489
186
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 11.488
187
ART010 Arteriolosclerosis 37 11.429
188
RCK004 Rickets 68 11.429
189
P GLM040 Glioma Susceptibility 1 71 11.389
191
NRN005 Neuronal Ceroid-Lipofuscinoses 61 11.316
192
P ATT013 Attention Deficit-Hyperactivity Disorder 64 11.264
193
P CRN300 Coronary Heart Disease 1 73 11.240
194
P RSP003 Respiratory Failure 74 11.226
195
ALZ052 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology 9 11.210
196
CNS004 Constipation 56 11.161
197
PST028 Post-Traumatic Stress Disorder 59 11.159
198
NRD075 Neurodegenerative Disease with Dementia 5 11.132
199
INS024 Insulin-Like Growth Factor I 78 11.113
200
P FRG001 Fragile X Syndrome 70 11.110
201
MLG169 Malignant Astrocytoma 57 11.088
202
HMN044 Human Immunodeficiency Virus Type 1 78 11.026
203
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 11.023
204
P RTN008 Retinitis Pigmentosa 80 10.988
205
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 10.945
206
48X005 48,xyyy 39 10.898
207
HYP056 Hypoglycemia 65 10.894
208
DMY004 Demyelinating Disease 50 10.864
209
CRB004 Cerebral Artery Occlusion 45 10.843
210
GLB002 Glioblastoma 67 10.787
211
P FRD001 Friedreich Ataxia 61 10.682
212
NMN001 Nominal Aphasia 40 10.678
213
P CHR345 Chronic Pain 50 10.596
214
WLL004 Wallerian Degeneration 38 10.572
215
SBC001 Subacute Sclerosing Panencephalitis 53 10.560
216
P ANP001 Anaplastic Large Cell Lymphoma 61 10.541
217
c HRD010 Hereditary Spastic Paraplegia 66 10.526
218
P MSC005 Muscular Dystrophy 67 10.444
219
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 10.441
220
P PRS038 Personality Disorder 65 10.435
221
HYP060 Hyperinsulinism 54 10.435
222
IRN002 Iron Metabolism Disease 57 10.395
223
P NMN002 Niemann-Pick Disease 60 10.391
224
ACQ007 Acquired Immunodeficiency Syndrome 59 10.273
225
GLC003 Glucose Intolerance 54 10.264
226
P MYT002 Myotonic Dystrophy 51 10.238
227
DMN012 Dementia - Subcortical 18 10.238
228
CNG034 Congestive Heart Failure 69 10.224
229
P NRC002 Narcolepsy 56 10.211
230
P ALC033 Alcohol Use Disorder 61 10.161
231
INC002 Inclusion Body Myositis 57 10.140
232
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 10.006
234
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 9.976
235
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 9.935
236
c MGR028 Migraine with or Without Aura 1 64 9.908
237
FRG010 Fragile X Tremor/ataxia Syndrome 44 9.870
238
P RTN018 Retinal Disease 53 9.856
239
END040 Endogenous Depression 55 9.827
240
PRG033 Progressive Non-Fluent Aphasia 52 9.763
241
BNR002 Bone Resorption Disease 47 9.724
242
c HNT011 Huntington Disease-Like 3 34 9.712
243
PLM129 Pulmonary Disease, Chronic Obstructive 74 9.702
244
P MYS005 Myositis 56 9.635
245
ACT084 Acute Stress Disorder 54 9.627
246
CHL123 Chlamydia 58 9.601
247
NRT004 Neuritis 53 9.586
248
c NMN015 Niemann-Pick Disease, Type C1 68 9.559
249
P HYP086 Hypothyroidism 69 9.535
250
STT001 Status Epilepticus 59 9.531
251
P HRT032 Heart Disease 81 9.526
252
RTN017 Retinal Detachment 60 9.494
253
HPT019 Hepatic Encephalopathy 59 9.471
254
PLY150 Polykaryocytosis Inducer 29 9.421
255
BCT022 Bacterial Infectious Disease 56 9.417
256
DSS008 Disease of Mental Health 74 9.370
257
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 9.342
258
c CHR684 Chronic Kidney Disease 69 9.279
259
SYN036 Syncope 45 9.258
260
ATS010 Autosomal Recessive Disease 42 9.227
261
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 9.137
262
P FTL002 Fatal Familial Insomnia 50 9.105
263
HPT004 Hepatic Coma 43 9.089
264
DNT005 Dentatorubral-Pallidoluysian Atrophy 60 8.971
265
P OLV001 Olivopontocerebellar Atrophy 51 8.910
266
GLM045 Glioma 63 8.885
267
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 8.835
268
SPC010 Speech and Communication Disorders 48 8.816
269
c HMC039 Hemochromatosis, Type 1 73 8.816
270
c OPT053 Optic Atrophy 1 62 8.747
271
P SKN015 Skin Carcinoma 71 8.711
272
P ATS364 Autism 69 8.619
273
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 8.604
274
SVR001 Severe Acute Respiratory Syndrome 67 8.581
275
OCL069 Ocular Motor Apraxia 57 8.574
276
GT001 Gout 64 8.573
277
CHL147 Chlamydia Pneumonia 47 8.571
278
SPN050 Spinocerebellar Degeneration 39 8.560
279
GLL048 Glial Tumor 52 8.514
280
DBT010 Diabetic Neuropathy 54 8.514
281
MTS001 Mutism 44 8.445
282
P PNM007 Pneumonia 67 8.386
283
ADR007 Adrenoleukodystrophy 73 8.371
284
TRD006 Tardive Dyskinesia 53 8.346
285
P MYP006 Myopia 56 8.326
286
OBS002 Obsessive-Compulsive Disorder 68 8.319
287
P MTC069 Mitochondrial Disorders 57 8.266
288
P MYS003 Myasthenia Gravis 68 8.254
289
FTT001 Fatty Liver Disease 62 8.210
290
P MCR010 Microcephaly 60 8.189
291
P DYS021 Dysautonomia 38 8.186
292
P CHR071 Charcot-Marie-Tooth Disease 64 8.157
293
MTC005 Mitochondrial Metabolism Disease 45 8.104
294
HMR039 Hemorrhage, Intracerebral 57 8.086
295
ADR022 Adrenomyeloneuropathy 39 8.045
296
c SPN294 Spinocerebellar Ataxia 1 53 8.044
297
RTN020 Retinal Vascular Disease 46 8.023
298
IMP005 Impotence 52 7.996
299
P RTN024 Retinoblastoma 73 7.985
300
TTH006 Tooth Disease 51 7.970
301
TRN015 Transient Cerebral Ischemia 63 7.939
302
LRN003 Learning Disability 49 7.918
303
BRN028 Brain Cancer 74 7.862
304
ASP007 Aspiration Pneumonia 49 7.822
305
KRT009 Keratosis 53 7.795
306
c SCN036 Secondary Progressive Multiple Sclerosis 55 7.785
307
P HYP265 Hypotonia 42 7.780
308
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 7.756
309
RLP002 Relapsing-Remitting Multiple Sclerosis 56 7.739
310
PSD088 Pseudobulbar Affect 33 7.737
311
PST092 Posttransplant Acute Limbic Encephalitis 28 7.733
312
LGP003 Logopenic Progressive Aphasia 23 7.727
313
P HYP069 Hyperparathyroidism 62 7.725
314
LGH007 Leigh Syndrome 70 7.703
315
P PTS002 Ptosis 52 7.682
316
VTM002 Vitamin B12 Deficiency 48 7.675
317
HTC003 Hutchinson-Gilford Progeria Syndrome 65 7.674
318
P RHM011 Rheumatoid Arthritis 82 7.642
319
P CRD246 Cardiovascular System Disease 56 7.631
320
P SBS003 Substance Abuse 54 7.622
321
NRM005 Neuromuscular Disease 63 7.516
322
ALL029 Allergic Disease 59 7.510
323
HND015 Hand Skill, Relative 30 7.472
324
CRB090 Cerebral Hypoxia 42 7.441
325
PRP030 Purpura 54 7.439
326
DYS003 Dysgraphia 35 7.435
327
HNS001 Hansen's Disease 32 7.428
328
P CRB059 Cerebellar Degeneration 36 7.421
329
ERL001 Early Myoclonic Encephalopathy 62 7.414
330
MNK001 Menkes Disease 64 7.399
331
P ART022 Arthritis 71 7.359
332
P LPR021 Leprosy 3 71 7.329
333
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.320
334
c ATR087 Atrial Standstill 1 74 7.315
335
P WLF004 Wolfram Syndrome 61 7.305
336
ANX004 Anoxia 40 7.258
337
PRT037 Pertussis 65 7.253
338
P BRB001 Beriberi 44 7.245
339
CRT015 Carotid Artery Occlusion 45 7.226
340
P INF037 Inflammatory Bowel Disease 53 7.203
341
IDM001 Ideomotor Apraxia 37 7.188
343
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 7.168
344
P KDN018 Kidney Disease 72 7.164
345
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 7.162
346
P GCH001 Gaucher's Disease 70 7.116
347
NRN008 Neuronal Intranuclear Inclusion Disease 47 7.112
348
CRB037 Cerebral Palsy 67 7.088
349
TTN003 Tetanus 65 7.064
350
KRN002 Kearns-Sayre Syndrome 63 7.056
351
PST027 Postencephalitic Parkinson Disease 46 7.053
352
NRX001 Neuroaxonal Dystrophy 38 7.039
353
PTH003 Pathologic Nystagmus 52 7.029
354
DBT007 Diabetic Cataract 36 7.028
355
P URN019 Urinary Tract Infection 49 6.999
356
BRN014 Bronchopneumonia 53 6.988
357
P DBT005 Diabetes Insipidus 54 6.971
358
P LCT001 Lactic Acidosis 51 6.961
359
NRT001 Neurotic Disorder 56 6.951
360
MYL069 Myeloma, Multiple 77 6.948
361
DFC004 Deficiency Anemia 74 6.932
362
P CRD119 Cardiac Arrest 67 6.929
363
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 6.898
364
P UVT001 Uveitis 57 6.883
365
CRB008 Cerebral Atherosclerosis 46 6.871
366
P DRR001 Diarrhea 55 6.853
367
P EXN002 Exanthem 58 6.846
369
OST012 Osteoarthritis 77 6.821
370
DSS032 Disease by Infectious Agent 55 6.766
371
P ATR011 Atrial Fibrillation 66 6.764
372
P SPN301 Spinocerebellar Ataxia 2 59 6.762
373
P MTC003 Metachromatic Leukodystrophy 71 6.741
374
P RST001 Restless Legs Syndrome 52 6.740
375
c ALM001 Al Amyloidosis 54 6.729
376
NRM001 Neuromyelitis Optica 61 6.723
377
P MLN008 Melanoma 76 6.719
378
ALX003 Alexander Disease 61 6.705
379
GRS011 Gerstmann-Straussler Disease 56 6.703
380
P BND020 Bone Disease 59 6.660
381
MCL006 Macular Retinal Edema 57 6.658
382
ETN001 Eating Disorder 59 6.653
383
SKN016 Skin Disease 63 6.653
384
AGR018 Agraphia 37 6.640
385
P MYC007 Myocardial Infarction 70 6.637
386
PRS045 Prostatic Hypertrophy 53 6.636
387
CVD001 Covid-19 57 6.614
388
P LKM002 Leukemia 67 6.606
389
P DRM053 Dermatitis, Atopic 65 6.605
390
MYC079 Myoclonic Epilepsy of Lafora 64 6.586
391
VSL003 Visual Agnosia 33 6.578
392
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 6.577
393
P SDR002 Siderosis 43 6.553
394
P AXN001 Axonal Neuropathy 35 6.502
395
HYP080 Hypogonadism 50 6.467
396
P STR001 Striatonigral Degeneration 37 6.456
397
BRN004 Brain Edema 54 6.438
398
WRN001 Werner Syndrome 69 6.433
399
MSL001 Measles 61 6.421
400
ATX019 Ataxia with Vitamin E Deficiency 44 6.419
401
PMP014 Pemphigoid 51 6.416
402
HRW001 Hair Whorl 35 6.410
403
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 6.392
404
LVR012 Liver Cirrhosis 63 6.379
405
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 6.376
406
PRP027 Peripheral Vascular Disease 71 6.358
407
ART002 Arts Syndrome 66 6.349
408
c INH020 Inherited Metabolic Disorder 48 6.310
409
P OPT009 Optic Neuritis 57 6.294
410
P GNG009 Gangliosidosis 44 6.283
411
c HYP595 Hypertension, Essential 85 6.282
412
OCL006 Ocular Hypertension 53 6.281
413
P RTT002 Rett Syndrome 79 6.276
414
BRN024 Bronchitis 67 6.272
415
WLS001 Wilson Disease 70 6.266
416
ADS004 Aids Dementia Complex 40 6.242
417
P LVR013 Liver Disease 69 6.239
418
VTM028 Vitamin E, Familial Isolated Deficiency of 53 6.231
419
PLM031 Poliomyelitis 63 6.226
420
SPC005 Speech Disorder 45 6.204
421
c LKM061 Leukemia, Acute Myeloid 83 6.198
422
PRS021 Prostatic Adenoma 43 6.172
423
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 63 6.169
424
P HYP076 Hyperthyroidism 53 6.155
425
P SNS001 Sensorineural Hearing Loss 59 6.153
426
XRD010 Xeroderma Pigmentosum, Variant Type 73 6.143
427
LPP008 Lipoprotein Quantitative Trait Locus 65 6.130
428
CHL014 Cholera 62 6.120
429
IMM167 Immune Deficiency Disease 78 6.113
430
WRN002 Wernicke-Korsakoff Syndrome 50 6.105
431
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 6.063
432
c WLF013 Wolfram Syndrome 1 60 6.036
433
P MYC026 Myoclonus Epilepsy 35 6.026
434
P CCK001 Cockayne Syndrome 68 6.016
435
c PRD040 Periodontitis, Chronic 52 6.014
436
APN008 Apnea, Obstructive Sleep 67 5.995
437
c HRD039 Hereditary Amyloidosis 45 5.986
438
MSC157 Muscular Dystrophy, Duchenne Type 79 5.956
439
P DYS005 Dyslexia 41 5.948
440
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 5.940
441
c NMN014 Niemann-Pick Disease, Type C2 49 5.917
442
DRM006 Dermatitis 62 5.904
443
CHR028 Chronic Wasting Disease 33 5.904
444
P TBR001 Tuberous Sclerosis 69 5.869
445
P HYP750 Hypertriglyceridemia, Familial 62 5.842
446
c TYP008 Type 1 Diabetes Mellitus 70 5.841
447
P GLL022 Guillain-Barre Syndrome 60 5.833
448
SBC025 Subcortical Arteriosclerotic Encephalopathy 19 5.812
449
P VSC011 Vasculitis 61 5.809
450
P MTC133 Mitochondrial Myopathy 50 5.766
451
c MCR112 Microvascular Complications of Diabetes 2 42 5.752
452
MMM001 Mammary Paget's Disease 53 5.748
453
AKN002 Akinetic Mutism 36 5.738
454
BSL009 Basal Ganglia Calcification 45 5.737
455
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 5.721
456
c HRD026 Hereditary Ataxia 47 5.714
457
P TYS001 Tay-Sachs Disease 69 5.694
458
PLM033 Pulmonary Embolism 58 5.692
459
c SCN007 Secondary Hyperparathyroidism 51 5.685
460
GRS001 Gerstmann Syndrome 41 5.664
461
P TCD001 Tic Disorder 49 5.646
462
PRS129 Prostatic Hyperplasia, Benign 49 5.642
463
PLG002 Plague 58 5.615
464
SPR066 Superficial Siderosis 38 5.607
465
c AMY009 Amyloidosis Aa 47 5.603
466
c SPN296 Spinocerebellar Ataxia 17 47 5.597
467
ENT004 Enthesopathy 51 5.592
468
ABT001 Abetalipoproteinemia 68 5.550
469
P CLC063 Celiac Disease 1 66 5.548
470
WRN003 Wernicke Encephalopathy 46 5.546
471
CPG001 Capgras Syndrome 26 5.520
472
c PRC016 Pre-Eclampsia 65 5.517
473
P KRB001 Krabbe Disease 69 5.499
474
TXC005 Toxic Shock Syndrome 62 5.492
475
P INF032 Infertility 57 5.481
476
CRB087 Cerebral Arteriosclerosis 17 5.480
477
P PNC044 Pancreatitis 61 5.475
478
NNL006 Non-Alcoholic Steatohepatitis 54 5.474
479
c PRG011 Progressive Myoclonus Epilepsy 41 5.472
480
P RHN004 Rhinitis 57 5.462
481
P SYP003 Syphilis 59 5.445
482
ACR006 Aceruloplasminemia 63 5.427
483
P HRD217 Hereditary Optic Neuropathy 36 5.424
484
LNG099 Lung Disease 62 5.413
485
P MCR129 Microvascular Complications of Diabetes 1 68 5.403
486
FBR047 Fibromyalgia 58 5.381
487
CRT013 Carotid Stenosis 51 5.367
488
P GST044 Gastritis 55 5.354
489
c MCR113 Microvascular Complications of Diabetes 3 52 5.352
490
CHL067 Cholecystitis 60 5.349
491
OST011 Osteomalacia 52 5.306
492
P STR020 Strabismus 56 5.299
493
MCH006 Mechanical Strabismus 40 5.299
494
c DLT002 Dilated Cardiomyopathy 78 5.297
495
PHY002 Physical Disorder 41 5.288
496
RBS001 Rabies 58 5.280
497
DYS009 Dysthymic Disorder 52 5.270
498
CHR105 Choreoacanthocytosis 55 5.262
499
P PRS040 Prostate Cancer 95 5.213
500
NRL016 Neural Tube Defects 81 5.206
501
P CLR023 Colorectal Cancer 100 5.199
502
P ACN011 Acne 57 5.174
503
ASY002 Asymptomatic Neurosyphilis 41 5.163
504
NRS003 Neurosyphilis 45 5.163
505
P PRS013 Prosopagnosia 36 5.151
506
P HMC002 Homocystinuria 53 5.146
507
ART140 Arteries, Anomalies of 53 5.142
508
P PGT001 Paget's Disease of Bone 61 5.141
509
ATN004 Autonomic Neuropathy 42 5.137
510
EXF001 Exfoliation Syndrome 56 5.134
511
c MCR120 Microvascular Complications of Diabetes 7 47 5.131
512
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 54 5.106
513
P CMM008 Communicating Hydrocephalus 45 5.105
514
c SPN291 Spinocerebellar Ataxia 7 53 5.091
515
MNG007 Manganese Poisoning 28 5.090
516
SND001 Sandhoff Disease 66 5.084
517
RFR003 Refractive Error 41 5.061
518
HRP009 Herpes Simplex Encephalitis 58 5.049
519
SML010 Simultanagnosia 32 5.047
520
KRT002 Keratomalacia 55 5.023
521
SNS003 Sensory Peripheral Neuropathy 52 5.018
522
ITR003 Iatrogenic Creutzfeldt-Jakob Disease 15 5.004
523
HLC007 Helicobacter Pylori Infection 67 5.003
524
c ERL056 Early-Onset Parkinson's Disease 40 4.999
525
c ATM075 Autoimmune Encephalitis 40 4.991
526
CRH001 Crohn's Disease 80 4.991
528
P OVR082 Overgrowth Syndrome 49 4.973
529
c DWL002 Dowling-Degos Disease 1 58 4.956
530
MCL003 Macular Holes 44 4.949
531
P HYP263 Hypersomnia 41 4.949
532
SPC030 Specific Language Disorder 25 4.941
533
ALX001 Alexia 44 4.929
534
CHC001 Chickenpox 57 4.924
535
RST023 Resting Heart Rate, Variation in 40 4.919
536
OCL015 Oculomotor Apraxia 39 4.917
537
VSC064 Vascular Parkinsonism 21 4.901
538
HST010 Histiocytosis 49 4.900
539
P HMN010 Hemangioma 62 4.886
540
MNN043 Meningioma, Familial 79 4.883
541
SPN021 Spinal Meningioma 50 4.883
542
GST019 Gastrointestinal Stromal Tumor 78 4.881
543
P MYL006 Myeloid Leukemia 61 4.854
544
P GNT009 Giant Axonal Neuropathy 46 4.852
545
c MCR130 Microvascular Complications of Diabetes 6 41 4.832
546
c MCR133 Microvascular Complications of Diabetes 4 41 4.832
547
PRR007 Perry Syndrome 52 4.829
548
LMB024 Limbic Encephalitis 43 4.814
549
GLL008 Gilles De La Tourette Syndrome 65 4.805
550
P ART023 Arthropathy 61 4.802
551
P PLM036 Pulmonary Fibrosis 66 4.782
552
c TBR025 Tuberous Sclerosis 1 84 4.763
553
HMP005 Hemiplegia 54 4.761
554
RTR001 Retrograde Amnesia 41 4.760
555
SPL018 Splenomegaly 49 4.725
556
CLS047 Classic Progressive Supranuclear Palsy Syndrome 33 4.724
557
P PSR002 Psoriasis 63 4.724
558
PST011 Pustulosis of Palm and Sole 52 4.724
559
PPT005 Peptic Ulcer Disease 58 4.722
560
ALL003 Allergic Rhinitis 67 4.721
561
P TXP001 Toxoplasmosis 60 4.719
562
ANT019 Anterograde Amnesia 38 4.707
563
CNV004 Canavan Disease 62 4.704
564
HYP264 Hypertonia 36 4.666
565
P ANT006 Antiphospholipid Syndrome 55 4.639
566
HYP068 Hyperostosis 47 4.628
567
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.617
568
PLM001 Pulmonary Tuberculosis 69 4.616
569
ULC004 Ulcerative Colitis 74 4.596
570
MDD018 Middle East Respiratory Syndrome 44 4.587
571
P BLD134 Bladder Cancer 79 4.582
572
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 4.555
573
P MYC084 Mycobacterium Tuberculosis 1 68 4.547
574
SXL003 Sexual Disorder 49 4.542
575
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 4.529
576
SCR001 Secretory Meningioma 40 4.527
577
LYM002 Lymphoplasmacyte-Rich Meningioma 35 4.527
578
P CRN025 Corneal Dystrophy 49 4.522
579
MTC004 Mitochondrial Encephalomyopathy 42 4.513
580
PRG009 Progressive Multifocal Leukoencephalopathy 58 4.481
581
GNR004 Generalized Anxiety Disorder 55 4.476
582
P PLM037 Pulmonary Hypertension 72 4.475
583
P NTR004 Neutropenia 63 4.472
584
DBT081 Diabetic Encephalopathy 36 4.463
585
HYP014 Hyperuricemia 51 4.462
586
c ACT027 Acute Pancreatitis 60 4.459
587
IRN001 Iron Deficiency Anemia 58 4.443
588
DYS004 Dyscalculia 35 4.443
589
CHR066 Chronic Fatigue Syndrome 60 4.441
590
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 56 4.440
591
AVD001 Avoidant Personality Disorder 49 4.432
592
FND002 Fundus Dystrophy 55 4.428
593
c GM1007 Gm1 Gangliosidosis 65 4.428
594
SWL001 Swallowing Disorders 38 4.421
595
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 4.418
596
c ACT068 Acute Cystitis 61 4.415
597
QDR001 Quadriplegia 50 4.413
598
c ADL066 Adult Neuronal Ceroid Lipofuscinosis 46 4.413
599
TRT001 Teratocarcinoma 42 4.406
600
END086 End Stage Renal Disease 52 4.395
601
P SPS008 Spastic Ataxia 41 4.375
602
LYM017 Lyme Disease 62 4.373
603
KFR001 Kufor-Rakeb Syndrome 59 4.363
604
P THL005 Thalassemia 56 4.362
605
CHM008 Chmp2b Frontotemporal Dementia 12 4.316
606
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 4.301
607
P NPH012 Nephrotic Syndrome 60 4.299
608
IRR002 Irritable Bowel Syndrome 65 4.295
609
P HDC001 Headache 57 4.290
610
XNT003 Xanthomatosis 49 4.287
611
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 4.287
612
PSD001 Pseudobulbar Palsy 38 4.286
613
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 4.283
614
GTP001 Gait Apraxia 29 4.279
615
HYP781 Hypoascorbemia 52 4.268
616
VCC001 Vaccinia 47 4.265
617
BCK006 Back Pain 47 4.263
618
c BCT007 Bacterial Meningitis 55 4.256
619
SCH012 Schizoaffective Disorder 50 4.248
620
GST050 Gastrointestinal System Disease 55 4.238
621
P BRS047 Breast Cancer 98 4.236
622
VRL011 Viral Infectious Disease 61 4.216
623
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 4.214
624
GNT189 Genetic Prion Disease 20 4.213
625
P TRN020 Turner Syndrome 67 4.210
626
STM007 Stomatitis 54 4.208
627
HRT012 Heart Valve Disease 53 4.205
628
HRP004 Herpes Zoster 61 4.200
629
P SCL018 Scoliosis 57 4.192
630
P LKM062 Leukemia, Acute Lymphoblastic 69 4.187
631
c INH030 Inherited Retinal Disorder 28 4.181
632
P AST005 Asthma 76 4.164
633
P VTR007 Vitreoretinopathy 46 4.158
634
DPH001 Diphtheria 59 4.134
635
P END033 Endocarditis 58 4.128
636
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.122
637
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 4.112
638
c MCP001 Mucopolysaccharidosis Iii 69 4.109
639
MLT116 Multiple System Atrophy, Parkinsonian Type 29 4.106
640
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.100
641
c LKM005 Leukemia, T-Cell, Chronic 34 4.100
642
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.088
643
THR024 Thrombosis 56 4.064
644
ENC005 Encephalomalacia 44 4.059
645
P HRD207 Hereditary Transthyretin Amyloidosis 25 4.057
646
CHL004 Cholelithiasis 49 4.056
647
VGN023 Vaginitis 56 4.054
648
DNT012 Dental Caries 53 4.047
649
NTR005 Nutritional Deficiency Disease 61 4.045
650
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 45 4.044
651
SPN051 Spondylitis 51 4.037
652
INF009 Inflammatory Spondylopathy 30 4.037
653
PPL049 Papillon-Lefevre Syndrome 66 4.027
654
P DDN001 Duodenal Ulcer 53 3.995
655
PRT251 Proteinuria, Chronic Benign 57 3.990
656
P LYM118 Lymphoma 67 3.976
657
ANG054 Angina Pectoris 66 3.974
658
ADN018 Adenoma 59 3.967
659
PRT036 Peritonitis 65 3.960
660
c MCL013 Mucolipidosis Iv 65 3.958
661
P HRD084 Hereditary Cerebral Amyloid Angiopathy 30 3.942
662
SQM006 Squamous Cell Carcinoma 60 3.942
663
P DMY001 Demyelinating Polyneuropathy 41 3.938
664
SPN020 Spondylosis 46 3.927
665
P MNN013 Meningitis 65 3.926
666
SPP007 Suppression Amblyopia 38 3.920
667
AMB002 Amblyopia 50 3.920
668
URM002 Uremia 47 3.906
669
DRG003 Drug Dependence 46 3.890
670
PRN009 Paranoid Schizophrenia 49 3.882
671
ADL002 Adult Syndrome 70 3.877
672
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 3.876
673
PRG001 Progressive Muscular Atrophy 41 3.858
674
P ALP008 Alopecia 54 3.851
675
GST023 Gastric Ulcer 52 3.848
676
c FML021 Familial Hypercholesterolemia 72 3.839
677
INT002 Intermittent Claudication 61 3.828
678
ANR007 Anorexia Nervosa 60 3.824
679
c VRL007 Viral Encephalitis 50 3.823
680
c SPS091 Spastic Paraplegia 4 27 3.816
681
TBC004 Tobacco Addiction 63 3.814
682
c PRM108 Primary Progressive Multiple Sclerosis 51 3.814
683
PHN003 Phenylketonuria 76 3.808
684
CNN005 Connective Tissue Disease 67 3.806
685
C9R003 C9orf72 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 11 3.805
686
c CHR095 Chronic Progressive External Ophthalmoplegia 49 3.803
687
SVR004 Severe Combined Immunodeficiency 72 3.802
688
RTN003 Retinal Ischemia 49 3.797
689
c FRN059 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 47 3.774
690
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 22 3.773
691
GTR002 Goiter 53 3.772
692
c SPN304 Spinocerebellar Ataxia 8 47 3.770
693
OVR063 Overnutrition 42 3.748
694
P GST053 Gastric Cancer 83 3.741
695
P PRG139 Progeroid Syndrome 27 3.738
696
MYL009 Myelodysplastic Syndrome 67 3.736
697
P GLM007 Glomerulonephritis 60 3.731
698
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 3.730
699
P CNJ013 Conjunctivitis 66 3.727
700
P HYP061 Hypertrophic Cardiomyopathy 69 3.724
701
EMB004 Embryonal Carcinoma 56 3.714
702
P NJM001 Nijmegen Breakage Syndrome 76 3.699
703
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 3.681
704
PRS047 Prostatitis 58 3.673
705
STF001 Stiff-Person Syndrome 58 3.668
706
MYL057 Myelopathy, Htlv-1-Associated 38 3.665
707
TRP002 Tropical Spastic Paraparesis 49 3.665
708
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 3.665
709
c SPN225 Spondyloarthropathy 1 70 3.651
710
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.642
711
MYS004 Myiasis 39 3.605
712
WHM001 Whim Syndrome 60 3.604
713
c SPN309 Spinocerebellar Ataxia 6 58 3.597
714
P CRP001 Carpal Tunnel Syndrome 66 3.597
715
c SCH079 Schizophrenia 1 44 3.595
716
c ACT071 Acute Kidney Failure 60 3.594
717
RHB024 Rhabdomyosarcoma 2 67 3.589
718
c ACT075 Acute Myocardial Infarction 56 3.585
719
P NRF002 Neurofibromatosis 57 3.581
720
ATR057 Atrioventricular Block 54 3.573
721
APP008 Appendicitis 62 3.568
722
P PNC025 Panic Disorder 52 3.561
723
HYP016 Hypochondriasis 47 3.550
724
c WLF009 Wolfram Syndrome 2 43 3.550
725
PRS025 Presbyopia 38 3.549
726
c GM2006 Gm2 Gangliosidosis 46 3.534
727
AYM001 Ayme-Gripp Syndrome 56 3.531
728
PRM290 Premature Centromere Division 20 3.519
729
P BLP003 Blepharospasm 46 3.504
730
CRD223 Cardiac Arrhythmia 63 3.496
731
ANT039 Antisynthetase Syndrome 55 3.493
732
KRT019 Keratitis, Hereditary 66 3.492
733
PRP080 Peripheral Artery Disease 54 3.486
734
ART004 Aortic Atherosclerosis 47 3.485
735
SRC014 Sarcoma 65 3.480
736
P ECL001 Eclampsia 52 3.474
737
APM001 Aapoaii Amyloidosis 14 3.471
738
TXC002 Toxic Encephalopathy 52 3.460
739
CRB089 Cerebral Beriberi 19 3.455
740
P SRC025 Sarcoidosis 1 71 3.454
741
P LNG032 Lung Cancer 98 3.444
742
HGH043 High Grade Glioma 45 3.437
743
ILS001 Ileus 50 3.405
744
P KDN017 Kidney Cancer 61 3.401
745
SPN035 Spindle Cell Sarcoma 54 3.396
746
c BCT013 Bacterial Pneumonia 48 3.396
747
c PRM038 Primary Agammaglobulinemia 47 3.394
748
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.388
749
HYP020 Hyperprolactinemia 63 3.388
750
END057 Endometrial Cancer 72 3.379
751
c THR092 Thrombophilia Due to Thrombin Defect 74 3.374
752
GST092 Gastroesophageal Reflux 61 3.374
753
FCL014 Focal Epilepsy 53 3.373
754
P PLY011 Polycystic Ovary Syndrome 57 3.372
755
P ADL017 Adult T-Cell Leukemia 56 3.368
756
MSC007 Muscle Hypertrophy 64 3.366
757
CRB009 Cerebritis 43 3.362
758
SKN005 Skin Atrophy 41 3.356
759
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 3.351
760
P MRC003 Mercury Poisoning 49 3.341
761
ACT119 Acute Promyelocytic Leukemia 62 3.340
762
c SPN312 Spinocerebellar Ataxia 14 46 3.339
763
P VNS003 Venous Insufficiency 55 3.334
764
P TRT010 Teratoma 51 3.329
765
P SYS005 Systemic Scleroderma 74 3.321
766
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 3.319
767
LWC001 Low Compliance Bladder 45 3.312
768
P MCL001 Mucolipidosis 49 3.304
769
OST159 Osteogenic Sarcoma 66 3.299
770
ADJ001 Adjustment Disorder 47 3.291
771
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 3.289
772
P MDL005 Medulloblastoma 75 3.287
773
c BLD140 Blood Group, I System 46 3.286
774
KRT071 Keratosis, Seborrheic 56 3.274
775
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.274
776
CNT047 Contact Dermatitis 57 3.271
777
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 3.268
778
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 3.267
779
MLN003 Melancholia 41 3.263
780
DBT006 Diabetic Macular Edema 48 3.249
781
P GRV001 Graves' Disease 55 3.231
782
P HYP098 Hypereosinophilic Syndrome 66 3.225
783
GRN059 Grn Frontotemporal Dementia 16 3.216
784
BWN006 Bowen's Disease 32 3.213
785
GRN017 Granulocytopenia 42 3.204
786
c SCL052 Scleroderma, Familial Progressive 61 3.200
787
P CRN026 Corneal Edema 42 3.199
788
HMN047 Human Cytomegalovirus Infection 57 3.189
789
P LNG064 Lung Cancer Susceptibility 3 70 3.188
790
c ATS438 Autosomal Recessive Spastic Ataxia 23 3.184
791
INV005 Inverted Follicular Keratosis 32 3.184
792
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 3.183
793
PRS064 Persistent Vegetative State 33 3.180
794
WTH001 Withdrawal Disorder 48 3.173
795
P ANR048 Aniridia 1 64 3.167
796
P GRF003 Graft-Versus-Host Disease 71 3.166
797
P HYP024 Hypoparathyroidism 55 3.159
798
IRD001 Iridocyclitis 53 3.154
799
P INF038 Influenza 68 3.142
800
KRT008 Keratopathy 46 3.141
801
P PLY041 Polymyositis 59 3.136
802
P MLG056 Malignant Hyperthermia 66 3.135
803
P MLN007 Male Infertility 56 3.131
804
INT075 Intracranial Hypertension 53 3.130
805
P TMP003 Temporal Arteritis 69 3.128
806
NRG002 Neurogenic Bladder 55 3.127
807
LRY022 Laryngoonychocutaneous Syndrome 43 3.126
808
FCH001 Fuchs' Endothelial Dystrophy 50 3.121
809
P PNC035 Pancreatic Cancer 86 3.115
810
P OVR042 Ovarian Cancer 88 3.108
811
P PRS049 Persistent Mullerian Duct Syndrome 52 3.100
812
P RTN022 Retinal Vein Occlusion 54 3.097
813
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 3.097
814
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 3.097
815
NRL004 Neuroleptic Malignant Syndrome 52 3.088
816
PSR001 Psoriatic Arthritis 62 3.083
817
KLV001 Kluver-Bucy Syndrome 34 3.080
818
c NRD032 Neurodegeneration with Brain Iron Accumulation 5 51 3.075
819
PRS011 Persian Gulf Syndrome 35 3.073
820
DBT004 Diabetic Polyneuropathy 50 3.069
821
BRX001 Bruxism 51 3.063
822
PRX001 Peroxisomal Disease 46 3.060
823
CLN039 Cln4 Disease 17 3.056
824
P PLZ001 Pelizaeus-Merzbacher Disease 65 3.055
825
SPN027 Spinal Stenosis 59 3.050
826
P LPS002 Liposarcoma 64 3.045
827
c PRK093 Parkinson Disease 8, Autosomal Dominant 49 3.035
828
FML035 Familial Hyperlipidemia 55 3.029
829
c BSL007 Basal Cell Carcinoma 68 3.021
830
P END044 Endometriosis 62 3.021
831
ALX002 Alexithymia 37 3.012
832
c MCP043 Mucopolysaccharidosis, Type Iiia 61 3.010
833
PRM024 Primary Angle-Closure Glaucoma 39 3.004
834
SPN187 Spinocerebellar Atrophy 23 3.003
835
c CNG216 Congenital Hydrocephalus 53 3.002
836
LYM027 Lymphopenia 56 2.994
837
P HMP007 Hemophilia 52 2.993
838
c HMN021 Human T-Cell Leukemia Virus Type 1 47 2.991
839
P PYL005 Pyelonephritis 57 2.985
840
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 2.973
841
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 2.973
842
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 2.973
843
P MJR007 Major Affective Disorder 1 42 2.970
844
CTR027 Cataract-Glaucoma 22 2.964
845
CHG001 Chagas Disease 66 2.963
846
DCB001 Decubitus Ulcer 62 2.960
847
DRV001 Dravet Syndrome 69 2.949
848
FNG001 Finger Agnosia 19 2.945
849
LWC002 Lowe Oculocerebrorenal Syndrome 68 2.943
850
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 57 2.943
851
CRB011 Cerebrotendinous Xanthomatosis 65 2.931
852
P PLY014 Polycystic Kidney Disease 69 2.924
853
UNV001 Unverricht-Lundborg Syndrome 53 2.923
854
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 2.922
856
P SMK004 Smoking As a Quantitative Trait Locus 3 44 2.919
857
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 2.910
858
ART016 Aortic Aneurysm 68 2.903
859
PNG002 Pain Agnosia 51 2.896
860
TBL029 Tubulin, Beta 28 2.894
861
VRC005 Varicose Veins 60 2.890
862
IGR001 Ige Responsiveness, Atopic 59 2.879
863
P CTN015 Cutaneous T Cell Lymphoma 48 2.879
864
MTB004 Metabolic Acidosis 48 2.863
865
PLR008 Pleurisy 50 2.861
866
PRT038 Protein-Energy Malnutrition 53 2.861
867
P ANG001 Angelman Syndrome 65 2.855
868
DLS001 Delusional Disorder 45 2.855
869
P SCK002 Sick Sinus Syndrome 55 2.847
870
NND010 Nondisjunction 34 2.831
871
BRC012 Brucellosis 66 2.828
872
c PRK085 Parkinson Disease 1, Autosomal Dominant 49 2.824
873
BCT021 Bacterial Sepsis 43 2.817
874
WST005 West Nile Virus 57 2.809
875
P WSK001 Wiskott-Aldrich Syndrome 72 2.790
876
MLR004 Malaria 80 2.788
877
CRB086 Cerebral Aneurysms 40 2.777
878
P DRM010 Dermatomyositis 61 2.772
879
P HPT021 Hepatitis 69 2.763
880
P FTL001 Fetal Alcohol Syndrome 55 2.763
881
GNG004 Ganglioglioma 53 2.762
882
P FML018 Familial Mediterranean Fever 73 2.761
883
P HML002 Hemolytic Anemia 62 2.753
884
P ADN016 Adenocarcinoma 63 2.753
885
P ORT004 Orthostatic Intolerance 63 2.749
886
GLC106 Glucocorticoid Resistance, Generalized 48 2.749
887
DWR001 Dwarfism 44 2.747
888
CRV043 Cervical Dystonia 46 2.744
889
PRM013 Premature Menopause 58 2.734
890
P CND004 Candidiasis 58 2.733
891
c PRM015 Primary Cerebellar Degeneration 30 2.732
892
P PRD006 Prader-Willi Syndrome 61 2.727
893
c HPT073 Hepatitis C Virus 71 2.723
894
c JVN010 Juvenile Rheumatoid Arthritis 66 2.719
895
BSL008 Basal Ganglia Disease 41 2.715
896
SCH014 Schistosomiasis 56 2.714
897
CLT003 Colitis 63 2.712
898
P LSS002 Lissencephaly 50 2.711
899
MCR018 Microcytic Anemia 47 2.710
900
RSC001 Rosacea 55 2.710
901
P THR014 Thrombocytopenia 66 2.710
902
P FML011 Familial Adenomatous Polyposis 71 2.707
903
c ACT073 Acute Leukemia 58 2.700
904
CHR682 Chronic Bilirubin Encephalopathy 37 2.694
905
c OTP006 Otopalatodigital Syndrome, Type I 60 2.688
906
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 2.688
907
TRC008 Trachoma 53 2.682
908
SBS004 Substance Dependence 47 2.681
909
ACD003 Acid Sphingomyelinase Deficiency 32 2.680
910
P CNR004 Cone-Rod Dystrophy 2 74 2.680
911
PRN011 Pernicious Anemia 53 2.678
912
ALN006 Alien Hand Syndrome 16 2.678
913
P PRX014 Proximal Spinal Muscular Atrophy 42 2.676
914
MCL079 Macular Telangiectasia Type 2 27 2.671
915
SDD001 Sudden Infant Death Syndrome 60 2.670
916
P RBL001 Rubella 58 2.668
917
SYR010 Syringomyelia, Noncommunicating Isolated 36 2.668
918
P SYR001 Syringomyelia 47 2.668
919
CRD132 Cardiac Conduction Defect 60 2.667
920
GNG011 Gingival Disease 54 2.663
921
SPN041 Spinal Cord Disease 55 2.662
922
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 2.655
923
WST001 West Syndrome 59 2.654