Search results for chronic progressive multiple sclerosis

1275 hits were found for chronic progressive multiple sclerosis

# Family MCID Name MIFTS Score
1
c SCN036 Secondary Progressive Multiple Sclerosis 52 4.540
2
P MLT020 Multiple Sclerosis 85 1.158
3
P LKM002 Leukemia 75 0.580
4
P HPT021 Hepatitis 75 0.525
5
ATM095 Autoimmune Disease 66 0.507
6
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.499
7
P LTR001 Lateral Sclerosis 58 0.483
8
DMY004 Demyelinating Disease 58 0.464
9
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.419
10
c SCL052 Scleroderma, Familial Progressive 60 0.409
11
c LKM071 Leukemia, Chronic Lymphocytic 75 0.403
12
P KDN018 Kidney Disease 69 0.383
13
MYL069 Myeloma, Multiple 86 0.382
14
c HPT001 Hepatitis C 73 0.357
15
P TBR001 Tuberous Sclerosis 69 0.346
16
LNG099 Lung Disease 67 0.346
17
c LKM004 Leukemia, B-Cell, Chronic 37 0.342
18
c CHR089 Chronic Kidney Failure 72 0.322
19
P NRV007 Nervous System Disease 75 0.317
20
P LYM118 Lymphoma 71 0.315
21
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.313
22
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.312
23
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.305
24
PRS047 Prostatitis 59 0.301
25
NRN002 Neuronitis 43 0.299
26
P PNC044 Pancreatitis 64 0.290
27
P LVR013 Liver Disease 76 0.290
28
c BLD140 Blood Group, I System 37 0.287
29
P MYL006 Myeloid Leukemia 69 0.282
30
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.280
31
c HPT016 Hepatitis B 68 0.276
32
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.275
33
P ART022 Arthritis 77 0.272
34
END072 Endotheliitis 46 0.264
35
c TBR025 Tuberous Sclerosis 1 63 0.263
36
CRB009 Cerebritis 41 0.262
37
P EPL164 Epilepsy 70 0.262
38
NRM005 Neuromuscular Disease 60 0.259
39
c LKM063 Leukemia, Chronic Myeloid 80 0.257
40
P NRP001 Neuropathy 63 0.249
41
AGN016 Aging 65 0.248
42
IMM136 Immune System Disease 57 0.247
43
c HPT073 Hepatitis C Virus 73 0.243
44
VRL011 Viral Infectious Disease 64 0.243
45
SPS057 Spasticity 41 0.241
46
NRT004 Neuritis 55 0.238
47
URN009 Urinary System Disease 58 0.237
48
P VNS003 Venous Insufficiency 53 0.231
49
DMN002 Dementia 68 0.231
50
RSP006 Respiratory System Disease 63 0.230
51
SKN016 Skin Disease 68 0.228
52
P BRS047 Breast Cancer 100 0.228
53
P CHR345 Chronic Pain 52 0.226
54
P ENC018 Encephalopathy 58 0.224
55
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.223
56
SKN027 Skin Conditions 48 0.217
57
MNT002 Mental Depression 60 0.216
58
c HPT003 Hepatitis a 63 0.214
59
P THY032 Thyroiditis 56 0.211
60
ANX010 Anxiety 72 0.211
61
P BLD051 Blood Coagulation Disease 38 0.210
62
MTR014 Motor Neuron Disease 62 0.209
63
P CRV039 Cervicitis 49 0.209
64
P PLM037 Pulmonary Hypertension 79 0.205
65
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.205
66
P HPT023 Hepatocellular Carcinoma 94 0.202
67
AST005 Asthma 83 0.201
68
P GRF003 Graft-Versus-Host Disease 72 0.199
69
P PRD008 Periodontitis 67 0.198
70
SPN041 Spinal Cord Disease 54 0.198
71
MLT157 Multiple System Atrophy 1 65 0.197
72
LYM024 Lymphatic System Disease 45 0.197
73
RTN023 Retinitis 52 0.197
74
P PRS040 Prostate Cancer 88 0.196
75
P DBT009 Diabetes Mellitus 72 0.196
76
CNN005 Connective Tissue Disease 65 0.195
77
P PLY019 Polyneuropathy 58 0.195
78
P MYP004 Myopathy 69 0.194
79
P ADN016 Adenocarcinoma 71 0.193
80
P RHM011 Rheumatoid Arthritis 91 0.193
81
PLS009 Plasma Cell Neoplasm 51 0.192
82
P GLM007 Glomerulonephritis 61 0.191
83
P HRT032 Heart Disease 80 0.190
84
c PRM108 Primary Progressive Multiple Sclerosis 50 0.187
85
c CHR417 Chronic Graft Versus Host Disease 65 0.187
86
c CNT035 Central Nervous System Disease 65 0.184
87
P PNM007 Pneumonia 70 0.184
88
VSC007 Vascular Disease 71 0.183
89
ISC004 Ischemia 66 0.183
90
ANR040 Aneurysm 61 0.182
91
CHR066 Chronic Fatigue Syndrome 67 0.180
92
OPT009 Optic Neuritis 53 0.180
93
MLN008 Melanoma 72 0.180
94
ACQ007 Acquired Immunodeficiency Syndrome 65 0.179
95
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.179
96
P LPS004 Lupus Erythematosus 69 0.179
97
P LYM026 Lymphoblastic Leukemia 66 0.178
98
P ALZ034 Alzheimer Disease 95 0.178
99
PDT025 Pediatric Multiple Sclerosis 40 0.177
100
HMT018 Hematopoietic Stem Cell Transplantation 58 0.176
101
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 0.166
102
HDC001 Headache 55 0.166
103
CNG034 Congestive Heart Failure 74 0.164
104
SPS003 Spastic Diplegia 55 0.161
105
LYM067 Lymphoid Leukemia 43 0.161
106
P NRM001 Neuromyelitis Optica 67 0.160
107
P ART023 Arthropathy 68 0.159
108
P AST007 Astrocytoma 66 0.159
109
SQM006 Squamous Cell Carcinoma 74 0.159
110
P ANR048 Aniridia 1 68 0.159
111
BCK006 Back Pain 46 0.158
112
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.158
113
ANR038 Anorexia Nervosa 1 21 0.155
114
BLD137 Blood Group--Ahonen 17 0.155
115
P DMY001 Demyelinating Polyneuropathy 46 0.155
116
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.155
117
LYM019 Lymphosarcoma 58 0.152
118
HYP266 Hypoxia 61 0.151
119
P GLM045 Glioma 61 0.151
120
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.151
121
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.149
122
APH002 Aphasia 58 0.149
123
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.148
124
P MNN013 Meningitis 71 0.148
125
END030 End Stage Renal Failure 59 0.147
126
c SYS001 Systemic Lupus Erythematosus 86 0.146
127
OTT002 Otitis Media 67 0.146
128
P CRB088 Cerebral Atrophy 38 0.145
129
P SYS005 Systemic Scleroderma 67 0.145
130
INT066 Interstitial Lung Disease 63 0.144
131
RHM027 Rheumatic Disease 62 0.144
132
P ESP024 Esophagitis 64 0.144
133
P ENC004 Encephalitis 66 0.144
134
P SCH015 Schizophrenia 71 0.141
135
ALR002 Al-Raqad Syndrome 30 0.141
136
P INF038 Influenza 77 0.140
137
MYL031 Myeloproliferative Neoplasm 64 0.140
138
DFF003 Diffuse Scleroderma 44 0.140
139
MSC004 Muscle Tissue Disease 39 0.140
140
P PNC035 Pancreatic Cancer 89 0.139
141
c PNS012 Paine Syndrome 52 0.139
142
MSC033 Muscle Disorders 53 0.139
143
ADN018 Adenoma 63 0.139
144
URT039 Urticaria 59 0.139
145
SRC014 Sarcoma 68 0.139
146
PLY020 Polyradiculoneuropathy 48 0.138
147
P BCL006 B-Cell Lymphomas 70 0.137
148
P MYC007 Myocardial Infarction 81 0.137
149
ART140 Arteries, Anomalies of 51 0.137
150
P MSC003 Muscular Atrophy 55 0.137
151
JNT002 Joint Disorders 60 0.136
152
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.136
153
SLP005 Sleep Disorder 59 0.135
154
P RSP003 Respiratory Failure 71 0.135
155
P CRN018 Coronary Artery Anomaly 69 0.135
156
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 35 0.135
157
VSC011 Vasculitis 66 0.135
158
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.135
159
THR024 Thrombosis 61 0.134
160
P AMY004 Amyloidosis 69 0.134
161
PRP019 Peripheral Nervous System Disease 53 0.133
162
ISC006 Ischemic Heart Disease 73 0.132
163
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 35 0.132
164
LVR012 Liver Cirrhosis 73 0.132
165
DRM006 Dermatitis 67 0.132
166
GST050 Gastrointestinal System Disease 66 0.131
167
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.130
168
OST017 Osteomyelitis 64 0.128
169
PRT036 Peritonitis 67 0.128
170
P PSR002 Psoriasis 65 0.128
171
ATN005 Autonomic Dysfunction 51 0.126
172
CNS004 Constipation 57 0.126
173
ENT004 Enthesopathy 38 0.126
174
P HYP069 Hyperparathyroidism 58 0.126
175
P PLM036 Pulmonary Fibrosis 68 0.125
176
CLC006 Calcinosis 51 0.125
177
CLT003 Colitis 63 0.125
178
P THR014 Thrombocytopenia 65 0.125
179
GNG013 Gingivitis 64 0.124
180
c VRL010 Viral Hepatitis 59 0.124
181
ALL014 Allergic Encephalomyelitis 37 0.123
182
P CND004 Candidiasis 61 0.123
183
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.122
184
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.122
185
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.122
186
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.122
187
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.122
188
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.122
189
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.122
190
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.122
191
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.122
192
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.122
193
P ART021 Arteriosclerosis 62 0.122
194
P CLL015 Collagen Disease 53 0.120
195
c INT072 Intestinal Pseudo-Obstruction 57 0.120
196
PRP030 Purpura 61 0.119
197
P UVT001 Uveitis 61 0.119
198
P PRK057 Parkinson Disease, Late-Onset 78 0.118
199
TMP001 Temporal Lobe Epilepsy 54 0.118
200
SPN186 Spinal Cord Injury 67 0.118
201
P INF032 Infertility 59 0.117
202
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.116
203
P DRR001 Diarrhea 60 0.116
204
P CRN300 Coronary Heart Disease 1 57 0.115
205
MYC033 Myoclonus 40 0.115
206
P RHN004 Rhinitis 62 0.115
207
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.115
208
BRR014 Barrett Esophagus 64 0.115
209
P MYP006 Myopia 56 0.114
210
PRD007 Periodontal Disease 64 0.114
211
P PYL005 Pyelonephritis 56 0.114
212
OST012 Osteoarthritis 88 0.114
213
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.114
214
P MSC005 Muscular Dystrophy 66 0.113
215
BRC012 Brucellosis 71 0.113
216
HPT082 Hepatic Adenomas, Familial 52 0.113
217
FSC004 Fasciitis 48 0.112
218
c TRC078 Trichohepatoenteric Syndrome 2 34 0.111
219
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.111
220
LYM133 Lymphoma, Hodgkin, Classic 78 0.111
221
MVM001 Movement Disease 40 0.111
222
CRB039 Cerebrovascular Disease 68 0.109
223
P TRM003 Tremor 54 0.109
224
MTH009 Mouth Disease 64 0.109
225
P MYC084 Mycobacterium Tuberculosis 1 69 0.108
226
P INT068 Intestinal Disease 65 0.107
227
P PLY014 Polycystic Kidney Disease 60 0.107
228
BRN071 Brain Injury 54 0.107
229
GLB002 Glioblastoma 74 0.106
230
NRN004 Neuroendocrine Tumor 58 0.106
231
c CHR431 Chronic Venous Insufficiency 47 0.105
232
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.105
233
P NTR004 Neutropenia 60 0.105
234
LYM007 Lymphangioleiomyomatosis 68 0.105
235
PSY004 Psychotic Disorder 72 0.104
236
DYS073 Dysphagia 47 0.102
237
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.102
238
P MYL005 Myelofibrosis 75 0.102
239
MYL001 Myelitis 52 0.101
240
ATM052 Autoimmune Disease 1 30 0.101
241
P DYS154 Dystonia 61 0.101
242
HMN044 Human Immunodeficiency Virus Type 1 71 0.100
243
ACT049 Acute Disseminated Encephalomyelitis 52 0.100
244
P RPD001 Rapidly Progressive Glomerulonephritis 48 0.100
245
BSL008 Basal Ganglia Disease 44 0.100
246
P INF037 Inflammatory Bowel Disease 52 0.099
247
MDD011 Mood Disorder 64 0.099
248
INS024 Insulin-Like Growth Factor I 83 0.099
249
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.098
250
P OST002 Osteoporosis 75 0.097
251
CHR008 Choroiditis 47 0.097
252
P NPH012 Nephrotic Syndrome 60 0.096
253
P HYP086 Hypothyroidism 62 0.096
254
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.095
255
PRP016 Paraplegia 53 0.095
256
BRN028 Brain Cancer 72 0.095
257
P CTR002 Cataract 60 0.095
258
MCR004 Macroglobulinemia 54 0.094
259
P HML002 Hemolytic Anemia 62 0.094
260
P SLP006 Sleep Apnea 65 0.093
261
EWN002 Ewing's Family of Tumors 49 0.093
262
P HYD006 Hydrocephalus 68 0.093
263
P MYS003 Myasthenia Gravis 73 0.093
264
DDN006 Duodenitis 46 0.093
265
PLM031 Poliomyelitis 64 0.093
266
P NRB001 Neuroblastoma 73 0.093
267
SPS019 Spastic Paraparesis 33 0.092
268
P SPN046 Spinal Muscular Atrophy 63 0.092
269
c MNN043 Meningioma, Familial 69 0.092
270
P LPM005 Lipomatosis 50 0.091
271
HML018 Homologous Wasting Disease 18 0.091
272
ACR006 Aceruloplasminemia 65 0.091
273
GT001 Gout 60 0.091
274
MGR028 Migraine with or Without Aura 1 55 0.091
275
BRN038 Bronchial Disease 58 0.091
276
ARC002 Arachnoiditis 45 0.090
277
APR001 Apraxia 52 0.089
278
P PRM006 Primary Biliary Cirrhosis 55 0.089
279
FXF002 Fox-Fordyce Disease 40 0.089
280
c MTR002 Mitral Valve Insufficiency 46 0.089
281
ART016 Aortic Aneurysm 70 0.089
282
TRG002 Trigeminal Neuralgia 60 0.089
283
HSH003 Hashimoto Thyroiditis 67 0.089
284
PST011 Pustulosis of Palm and Sole 47 0.089
285
P ASP006 Aspergillosis 65 0.088
286
DFF005 Diffuse Large B-Cell Lymphoma 64 0.088
287
CRH001 Crohn's Disease 80 0.088
288
HYP066 Hyperglycemia 64 0.088
289
IMM158 Immune Suppression 57 0.088
290
P TCL004 T-Cell Leukemia 50 0.087
291
P ACT074 Acute Lymphocytic Leukemia 61 0.087
292
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.087
293
ALP046 Alport Syndrome, X-Linked 74 0.086
294
c INF145 Infantile Liver Failure Syndrome 1 33 0.086
295
CRN031 Cranial Nerve Disease 45 0.086
296
HYP264 Hypertonia 32 0.086
297
P RNG031 Ring Chromosome Y Syndrome 29 0.085
298
SPN051 Spondylitis 55 0.084
299
HDN002 Head Injury 48 0.084
300
P MYS005 Myositis 63 0.084
301
P SZR006 Seizure Disorder 55 0.084
302
TRM010 Traumatic Brain Injury 54 0.083
303
ANG054 Angina Pectoris 53 0.083
304
c ACT073 Acute Leukemia 61 0.083
305
RST001 Restless Legs Syndrome 54 0.083
306
P CNJ013 Conjunctivitis 67 0.082
307
PRP027 Peripheral Vascular Disease 71 0.082
308
STR067 Stroke, Ischemic 84 0.082
309
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.082
310
CHG001 Chagas Disease 72 0.082
311
GNG011 Gingival Disease 50 0.082
312
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.082
313
P HRP006 Herpes Simplex 70 0.082
314
NRV006 Nervous System Cancer 61 0.082
315
P MYC008 Myocarditis 58 0.082
316
P DRM010 Dermatomyositis 65 0.081
317
CHL067 Cholecystitis 58 0.081
318
BRN106 Burns 57 0.081
319
c BSL007 Basal Cell Carcinoma 66 0.081
320
P LYM025 Lymphedema 63 0.081
321
P ALP008 Alopecia 56 0.081
322
P TRN034 Transverse Myelitis 53 0.081
323
P PLM034 Pulmonary Emphysema 59 0.081
324
GST092 Gastroesophageal Reflux 64 0.081
325
P MJR001 Major Depressive Disorder 70 0.080
326
PNN001 Panniculitis 48 0.080
327
P DYS021 Dysautonomia 47 0.080
328
P PLY041 Polymyositis 57 0.080
329
SCH014 Schistosomiasis 62 0.080
330
LYM017 Lyme Disease 68 0.080
331
P RBL001 Rubella 61 0.079
332
PCK003 Pick Disease of Brain 66 0.079
333
PRC013 Pericarditis 55 0.079
334
c CHR037 Chronic Eosinophilic Pneumonia 49 0.079
335
HMT002 Hematologic Cancer 64 0.079
336
P OLG002 Oligodendroglioma 59 0.079
337
TRP002 Tropical Spastic Paraparesis 58 0.079
338
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.079
339
MDS022 Mediastinitis 44 0.079
340
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.078
341
ADR007 Adrenoleukodystrophy 72 0.078
342
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.078
343
SNS001 Sensorineural Hearing Loss 59 0.078
344
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.078
345
c SPN225 Spondyloarthropathy 1 71 0.078
346
CHR415 Chronic Venous Leg Ulcers 38 0.078
347
c ATM011 Autoimmune Hepatitis 63 0.077
348
INF009 Inflammatory Spondylopathy 32 0.077
349
P KDN017 Kidney Cancer 66 0.077
350
GLB015 Glioblastoma Multiforme 68 0.077
351
ALL026 Allergic Hypersensitivity Disease 59 0.077
352
SYN007 Synovitis 61 0.077
353
BLC015 Balo Concentric Sclerosis 35 0.077
354
P CYS018 Cystitis 57 0.077
355
WHP002 Whiplash 39 0.077
356
PNN005 Panencephalitis, Subacute Sclerosing 44 0.076
357
c LCL006 Localized Scleroderma 66 0.076
358
TTH006 Tooth Disease 54 0.076
359
P TRC086 Trichohepatoenteric Syndrome 1 54 0.076
360
c LKM062 Leukemia, Acute Lymphoblastic 64 0.076
361
LYM027 Lymphopenia 56 0.076
362
BLD044 Bladder Disease 55 0.076
363
MYC006 Mycosis Fungoides 73 0.076
364
P HST010 Histiocytosis 60 0.075
365
c CHR418 Chronic Leukemia 46 0.075
366
MCL006 Macular Retinal Edema 51 0.075
367
P ESN008 Eosinophilic Pneumonia 55 0.075
368
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.075
369
c BRN108 Branchiootic Syndrome 1 47 0.075
370
P PRT013 Portal Hypertension 59 0.075
371
NRG002 Neurogenic Bladder 53 0.075
372
P HYP098 Hypereosinophilic Syndrome 65 0.075
373
MXD005 Mixed Connective Tissue Disease 66 0.075
374
c MCR113 Microvascular Complications of Diabetes 3 55 0.075
375
P CHR071 Charcot-Marie-Tooth Disease 67 0.074
376
P ATS364 Autism 70 0.074
377
PMS001 Poems Syndrome 64 0.074
378
BRN012 Bronchiolitis Obliterans 60 0.074
379
P MDL005 Medulloblastoma 76 0.074
380
P END033 Endocarditis 58 0.074
381
P PRP029 Porphyria 62 0.074
382
P END044 Endometriosis 71 0.074
383
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.074
384
GST045 Gastroenteritis 65 0.074
385
DSC009 Discoid Lupus Erythematosus 48 0.074
386
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.073
387
CRY004 Cryoglobulinemia 49 0.073
388
MSL001 Measles 64 0.073
389
LKD001 Leukodystrophy 57 0.073
390
RTN018 Retinal Disease 56 0.073
391
BRN002 Bronchiolitis 59 0.073
392
FBR012 Fabry Disease 72 0.073
393
CHN070 Cohen-Gibson Syndrome 51 0.073
394
P MCR115 Microvascular Complications of Diabetes 5 66 0.073
395
LPD008 Lipid Metabolism Disorder 59 0.073
396
c MYS011 Myasthenia Gravis Congenital 28 0.072
397
HRP004 Herpes Zoster 61 0.072
398
P DLT002 Dilated Cardiomyopathy 76 0.072
399
PNG002 Pain Agnosia 41 0.072
400
DBT010 Diabetic Neuropathy 60 0.072
401
P CLS010 Cluster Headache 47 0.072
402
P ALC004 Alcohol Abuse 63 0.072
403
URM002 Uremia 52 0.072
404
PHR003 Pharyngitis 59 0.072
405
P CTN015 Cutaneous T Cell Lymphoma 56 0.072
406
THR004 Thrombocytosis 55 0.071
407
P CHL066 Cholangitis 52 0.071
408
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.071
409
HMS001 Hemosiderosis 50 0.071
410
P FCL005 Focal Segmental Glomerulosclerosis 60 0.071
411
INS001 Insulinoma 66 0.071
412
c NRM008 Neuromyelitis Optica Spectrum Disorder 30 0.071
413
P AGG001 Aggressive Periodontitis 55 0.071
414
c ACT075 Acute Myocardial Infarction 64 0.071
415
BLD163 Blood Group, Dombrock System 23 0.071
416
BNF002 Bone Fracture 56 0.070
417
TND004 Tendinopathy 45 0.070
418
NSP002 Nasopharyngitis 46 0.070
419
HYP060 Hyperinsulinism 56 0.070
420
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.070
421
TTN003 Tetanus 65 0.070
422
P DRM053 Dermatitis, Atopic 68 0.070
423
c MCR130 Microvascular Complications of Diabetes 6 42 0.070
424
c MCR120 Microvascular Complications of Diabetes 7 34 0.070
425
c MCR133 Microvascular Complications of Diabetes 4 32 0.070
426
CHL123 Chlamydia 64 0.070
427
GST019 Gastrointestinal Stromal Tumor 74 0.070
428
P RTN016 Retinal Degeneration 56 0.070
429
c CHR579 Chiari Malformation Type Ii 42 0.069
430
HRY003 Hairy Cell Leukemia 60 0.069
431
MLR004 Malaria 86 0.069
432
NRF007 Neurofibroma 65 0.069
433
PLM033 Pulmonary Embolism 62 0.069
434
QFV001 Q Fever 61 0.069
435
THY028 Thyroid Cancer 72 0.069
436
P SPN052 Spondyloarthropathy 61 0.069
437
P FNC043 Fanconi Anemia, Complementation Group E 52 0.069
438
P HYP265 Hypotonia 40 0.069
439
P HYP726 Hypercalcemia, Infantile, 1 57 0.069
440
CRS001 Crescentic Glomerulonephritis 44 0.069
441
BLL006 Bullous Pemphigoid 64 0.069
442
P PLY018 Polycythemia 60 0.069
443
CRT072 Creutzfeldt-Jakob Disease 65 0.069
444
PLM010 Pulmonary Edema 57 0.069
445
OPT006 Optic Nerve Disease 53 0.069
446
c ACT027 Acute Pancreatitis 61 0.068
447
PRN021 Paranasal Sinus Disease 51 0.068
448
P CMR001 Camurati-Engelmann Disease 62 0.068
449
TCD001 Tic Disorder 54 0.068
450
c TBR026 Tuberous Sclerosis 2 65 0.068
451
FTD001 Foot Drop 35 0.068
452
PSR001 Psoriatic Arthritis 66 0.068
453
PRS063 Paresthesia 36 0.067
454
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.067
455
P SCL057 Scoliosis, Isolated 1 28 0.067
456
NRR001 Neuroretinitis 46 0.067
457
HLC007 Helicobacter Pylori Infection 64 0.067
458
MYL057 Myelopathy, Htlv-1-Associated 38 0.067
459
P EHL001 Ehlers-Danlos Syndrome 61 0.067
460
HYP056 Hypoglycemia 62 0.067
461
GRN017 Granulocytopenia 49 0.067
462
INT042 Internuclear Ophthalmoplegia 40 0.067
463
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.067
464
GNR004 Generalized Anxiety Disorder 53 0.067
465
CYT008 Cytomegalovirus Infection 57 0.067
466
P HMP007 Hemophilia 61 0.067
467
PPL022 Papilloma 58 0.066
468
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.066
469
P FML018 Familial Mediterranean Fever 73 0.066
470
P EXN002 Exanthem 62 0.066
471
APL001 Aplastic Anemia 74 0.066
472
MLT075 Multifocal Motor Neuropathy 45 0.066
473
CNT047 Contact Dermatitis 64 0.066
474
ESN015 Eosinophilic Fasciitis 52 0.066
475
PRR002 Pure Red-Cell Aplasia 52 0.065
476
c THR092 Thrombophilia Due to Thrombin Defect 61 0.065
477
P SYR001 Syringomyelia 49 0.065
478
TXC002 Toxic Encephalopathy 55 0.065
479
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.065
480
P HRD009 Hereditary Wilms' Tumor 46 0.065
481
PLM012 Pulmonary Sarcoidosis 58 0.065
482
HMP005 Hemiplegia 54 0.065
483
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.065
484
P SDR002 Siderosis 48 0.065
485
ALL003 Allergic Rhinitis 68 0.064
486
P PHC003 Pheochromocytoma 72 0.064
487
PST028 Post-Traumatic Stress Disorder 59 0.064
488
c ADL017 Adult T-Cell Leukemia 63 0.064
489
P ART084 Arteriovenous Fistula 46 0.064
490
P PLY017 Polyarteritis Nodosa 51 0.064
491
c ACT135 Acute Graft Versus Host Disease 57 0.064
492
P HMN010 Hemangioma 61 0.064
493
c PRM005 Primary Hyperparathyroidism 59 0.064
494
MNN017 Mononeuropathy 42 0.063
495
P PRC012 Pericardial Effusion 52 0.063
496
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.063
497
c ART101 Aortic Valve Disease 2 65 0.063
498
P SYP003 Syphilis 55 0.063
499
P TXP001 Toxoplasmosis 65 0.063
500
CHR100 Chronic Ulcer of Skin 46 0.063
501
END081 Endosteal Hyperostosis, Autosomal Dominant 55 0.063
502
P PRP003 Porphyria Cutanea Tarda 67 0.063
503
P INT030 Intracranial Aneurysm 58 0.063
504
SLC006 Silicosis 57 0.063
505
PNM008 Pneumothorax 57 0.062
506
MNG003 Mungan Syndrome 34 0.062
507
P EPN002 Ependymoma 53 0.062
508
CLC001 Calciphylaxis 53 0.062
509
ESP023 Esophageal Disease 58 0.062
510
P DBT005 Diabetes Insipidus 54 0.062
511
P HYP024 Hypoparathyroidism 55 0.062
512
RNL011 Renal Osteodystrophy 49 0.062
513
LSH001 Leishmaniasis 71 0.062
514
P CLC063 Celiac Disease 1 65 0.062
515
P LPR021 Leprosy 3 59 0.062
516
P NRC002 Narcolepsy 64 0.062
517
ACT119 Acute Promyelocytic Leukemia 64 0.062
518
PNC001 Pancytopenia 50 0.062
519
P BPL003 Bipolar Disorder 61 0.062
520
VRC005 Varicose Veins 64 0.062
521
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.061
522
STT001 Status Epilepticus 60 0.061
523
NRS005 Neurosarcoidosis 26 0.061
524
PLY001 Polycythemia Vera 75 0.061
525
P PTT006 Pituitary Adenoma 57 0.061
526
HMF008 Hemifacial Atrophy, Progressive 44 0.061
527
LMB062 Limb Ischemia 52 0.061
528
PRC002 Paracoccidioidomycosis 59 0.061
529
STM007 Stomatitis 52 0.061
530
P KRT007 Keratoconus 49 0.061
531
P MTC003 Metachromatic Leukodystrophy 72 0.061
532
P PNM006 Pneumoconiosis 55 0.061
533
OBS002 Obsessive-Compulsive Disorder 68 0.060
534
SWL001 Swallowing Disorders 36 0.060
535
PLM001 Pulmonary Tuberculosis 72 0.060
536
MNN009 Meningoencephalitis 49 0.060
537
BRS064 Bursitis 42 0.060
538
HYP020 Hyperprolactinemia 64 0.060
539
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.060
540
IDP011 Idiopathic Interstitial Pneumonia 60 0.060
541
CRB037 Cerebral Palsy 70 0.060
542
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.060
543
ASP003 Aseptic Meningitis 54 0.060
544
CMM004 Common Variable Immunodeficiency 71 0.060
545
c WLM011 Wilms Tumor 6 44 0.060
546
P NSP012 Nasopharyngeal Carcinoma 71 0.060
547
P LCH002 Lichen Planus 58 0.059
548
P PRL003 Proliferative Glomerulonephritis 45 0.059
549
P CRB059 Cerebellar Degeneration 40 0.059
550
TRN018 Transitional Cell Carcinoma 58 0.059
551
CRB086 Cerebral Aneurysms 42 0.059
552
NNL002 Nonalcoholic Steatohepatitis 56 0.059
553
SPN020 Spondylosis 52 0.059
554
P STR035 Streptococcal Group a Invasive Disease 28 0.059
555
SPC005 Speech Disorder 44 0.059
556
P MYT002 Myotonic Dystrophy 50 0.059
557
PYD002 Pyoderma 51 0.058
558
P CNT005 Central Nervous System Lymphoma 57 0.058
559
PNC119 Pancreatic Neuroendocrine Tumor 49 0.058
560
LCH009 Lichen Sclerosus 45 0.058
561
P ORT004 Orthostatic Intolerance 68 0.058
562
INT075 Intracranial Hypertension 53 0.058
563
GLC003 Glucose Intolerance 58 0.058
564
THY030 Thyroid Gland Disease 51 0.058
565
ATN002 Autonomic Nervous System Disease 51 0.058
566
SYS004 Systemic Mastocytosis 65 0.058
567
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.058
568
OST003 Osteonecrosis 63 0.058
569
PRP036 Peripheral T-Cell Lymphoma 48 0.058
570
ANX004 Anoxia 49 0.057
571
MRK001 Merkel Cell Carcinoma 59 0.057
572
P ANP001 Anaplastic Large Cell Lymphoma 60 0.057
573
P ANT006 Antiphospholipid Syndrome 59 0.057
574
KWS002 Kawasaki Disease 72 0.057
575
P CTN003 Cutaneous Lupus Erythematosus 53 0.057
576
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.057
577
P CRN035 Cranial Nerve Palsy 42 0.057
578
CHR001 Churg-Strauss Syndrome 51 0.057
579
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.057
580
NCR004 Nocardiosis 43 0.057
581
ARC007 Arachnoid Cysts 39 0.057
582
P AXN001 Axonal Neuropathy 38 0.057
583
c JVN010 Juvenile Rheumatoid Arthritis 71 0.057
584
PYD001 Pyoderma Gangrenosum 55 0.057
585
ANG020 Angiosarcoma 57 0.057
586
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.057
587
c LPM012 Lipomatosis, Multiple 64 0.057
588
HYP068 Hyperostosis 52 0.057
589
RCK004 Rickets 63 0.057
590
ACR007 Acromegaly 70 0.057
591
c HPT007 Hepatitis E 57 0.057
592
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.057
593
HMP001 Hemopericardium 34 0.056
594
P BRY005 Beryllium Disease 43 0.056
595
P FNC004 Fanconi Syndrome 54 0.056
596
ALP072 Alpha-Fetoprotein Deficiency 32 0.056
597
P GRV001 Graves' Disease 62 0.056
598
KPS004 Kaposi Sarcoma 73 0.056
599
FCL003 Facial Hemiatrophy 31 0.056
600
SFT003 Soft Tissue Sarcoma 58 0.056
601
PRN023 Prion Disease 51 0.056
602
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.056
603
IRR002 Irritable Bowel Syndrome 63 0.056
604
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 54 0.056
605
c ATM022 Autoimmune Myocarditis 40 0.056
606
c CHR576 Chronic Beryllium Disease 42 0.056
607
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.056
608
P MCR010 Microcephaly 57 0.055
609
P VNT002 Ventricular Septal Defect 59 0.055
610
P PTS002 Ptosis 50 0.055
611
APN008 Apnea, Obstructive Sleep 67 0.055
612
LYM021 Lymphadenitis 62 0.055
613
MTC069 Mitochondrial Disorders 49 0.055
614
INC002 Inclusion Body Myositis 64 0.055
615
ALX002 Alexithymia 40 0.055
616
CRN030 Coronary Stenosis 52 0.055
617
FLR002 Filariasis 58 0.055
618
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.055
619
CRT049 Critical Limb Ischemia 56 0.055
620
ALL010 Allergic Contact Dermatitis 60 0.055
621
c ANT034 Anterior Uveitis 53 0.055
622
WRN001 Werner Syndrome 70 0.055
623
P SPN301 Spinocerebellar Ataxia 2 56 0.055
624
P HMR012 Hemorrhagic Fever 60 0.055
625
P SRC025 Sarcoidosis 1 63 0.054
626
HPT019 Hepatic Encephalopathy 59 0.054
627
ANG037 Angiomatosis 36 0.054
628
P SCL015 Scleritis 50 0.054
629
LMY002 Leiomyoma 58 0.054
630
TRY001 Trypanosomiasis 55 0.054
631
ADP007 Adie Pupil 41 0.054
632
P PRT026 Parotitis 45 0.054
633
NPH009 Nephrolithiasis 57 0.054
634
ECH003 Echinococcosis 57 0.054
635
c VRL007 Viral Encephalitis 53 0.054
636
WLL004 Wallerian Degeneration 40 0.054
637
SPR066 Superficial Siderosis 40 0.054
638
MSC157 Muscular Dystrophy, Duchenne Type 74 0.054
639
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.054
640
P HYP076 Hyperthyroidism 56 0.054
641
GST040 Gastric Adenocarcinoma 60 0.053
642
SPN369 Spinal Disease 42 0.053
643
ERY003 Erythema Multiforme 60 0.053
644
CRT015 Carotid Artery Occlusion 42 0.053
645
TST014 Testicular Cancer 54 0.053
646
CRD001 Cardiac Tamponade 45 0.053
647
CMP010 Complex Regional Pain Syndrome 58 0.053
648
CLR030 Clear Cell Renal Cell Carcinoma 55 0.053
649
c SZR022 Seizures, Benign Familial Neonatal, 1 39 0.053
650
DWN001 Down Syndrome 70 0.053
651
ILT001 Ileitis 52 0.053
652
c WLM018 Wilms Tumor 5 49 0.053
653
ALC006 Alcoholic Hepatitis 62 0.053
654
SCK005 Sickle Cell Disease 54 0.053
655
MRF001 Marfan Syndrome 75 0.053
656
WLL001 Williams-Beuren Syndrome 63 0.053
657
c PRM226 Primary Central Nervous System Lymphoma 51 0.053
658
NPH010 Nephrosclerosis 46 0.053
659
QDR001 Quadriplegia 54 0.053
660
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.053
661
EPD070 Epidermoid Cysts 46 0.053
662
STR020 Strabismus 55 0.052
663
OCL011 Ocular Motility Disease 31 0.052
664
WBR001 Weber Syndrome 40 0.052
665
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.052
666
P RTN022 Retinal Vein Occlusion 53 0.052
667
LMB024 Limbic Encephalitis 42 0.052
668
NRS003 Neurosyphilis 44 0.052
669
c ATR087 Atrial Standstill 1 59 0.052
670
RFR010 Refractory Anemia 48 0.052
671
P MCH002 Machado-Joseph Disease 63 0.052
672
INT003 Intracranial Hypotension 36 0.052
673
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.052
674
CPL005 Capillary Disease 38 0.052
675
P LPD010 Lipodystrophy 57 0.052
676
ISL001 Islet Cell Tumor 54 0.051
677
P ALP009 Alopecia Areata 64 0.051
678
c BCT007 Bacterial Meningitis 59 0.051
679
P GNT008 Giant Cell Tumor 49 0.051
680
PHT003 Phototoxic Dermatitis 39 0.051
681
P HNT016 Huntington Disease 78 0.051
682
RHM028 Rheumatic Heart Disease 54 0.051
683
APP008 Appendicitis 64 0.051
684
MCR088 Microscopic Polyangiitis 58 0.051
685
P PNV001 Panuveitis 52 0.051
686
OST011 Osteomalacia 52 0.051
687
CRP001 Carpal Tunnel Syndrome 64 0.050
688
RTN001 Retinal Vasculitis 47 0.050
689
BLP005 Blepharitis 43 0.050
690
KRT006 Keratoconjunctivitis 56 0.050
691
c ACT134 Acute Liver Failure 52 0.050
692
MTR031 Motor Neuro-Ophthalmic Disorders 20 0.050
693
P RTT002 Rett Syndrome 82 0.050
694
CRS005 Crest Syndrome 43 0.050
695
MGC001 Megacolon 50 0.050
696
c ACT071 Acute Kidney Failure 54 0.050
697
END021 Endomyocardial Fibrosis 51 0.050
698
CRD119 Cardiac Arrest 63 0.050
699
GNG004 Ganglioglioma 51 0.050
700
c ATS007 Autism Spectrum Disorder 68 0.050
701
FBR009 Fibrous Dysplasia 49 0.050
702
GNG002 Ganglioneuroma 50 0.049
703
HST009 Histiocytoma 51 0.049
704
c ATM075 Autoimmune Encephalitis 40 0.049
705
DPH001 Diphtheria 63 0.049
706
MTS001 Mutism 42 0.049
707
SCH012 Schizoaffective Disorder 51 0.049
708
ALL009 Allergic Conjunctivitis 53 0.049
709
c CHL119 Cholangitis, Primary Sclerosing 60 0.049
710
EWN003 Ewing Sarcoma 72 0.049
711
BNN003 Bone Inflammation Disease 46 0.049
712
CHR073 Choreatic Disease 40 0.049
713
GLL008 Gilles De La Tourette Syndrome 64 0.049
714
CLL021 Collagenous Colitis 43 0.049
715
PPL021 Papilledema 50 0.049
716
MLD001 Melioidosis 73 0.049
717
CNT046 Central Nervous System Vasculitis 47 0.048
718
LRG008 Large Granular Lymphocyte Leukemia 49 0.048
719
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 70 0.048
720
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.048
721
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.048
722
BRN018 Borna Disease 38 0.048
723
FLL008 Folliculitis 50 0.048
724
VTM002 Vitamin B12 Deficiency 46 0.048
725
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.048
726
P TMP003 Temporal Arteritis 67 0.048
727
HRT012 Heart Valve Disease 45 0.048
728
BRN014 Bronchopneumonia 45 0.048
729
LNG108 Langerhans Cell Histiocytosis 63 0.048
730
P ECL001 Eclampsia 57 0.048
731
PLY150 Polykaryocytosis Inducer 20 0.048
732
BTN003 Biotinidase Deficiency 56 0.048
733
MMB001 Membranoproliferative Glomerulonephritis 51 0.048
734
P FRD012 Friedreich Ataxia 1 58 0.048
735
LYM022 Lymphangioma 53 0.048
736
SPN027 Spinal Stenosis 60 0.048
737
c CNT015 Central Sleep Apnea 45 0.048
738
P RHB003 Rhabdomyosarcoma 61 0.048
739
STF001 Stiff-Person Syndrome 61 0.047
740
PTT009 Pituitary Gland Disease 56 0.047
741
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.047
742
RHM001 Rheumatic Fever 59 0.047
743
c HMP029 Hemophilia a 69 0.047
744
CRT013 Carotid Stenosis 52 0.047
745
CRY005 Cryptococcosis 54 0.047
746
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.047
747
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.047
748
ALL006 Allergic Asthma 60 0.047
749
PRN011 Pernicious Anemia 50 0.047
750
P THR015 Thrombophilia 58 0.047
751
ADT003 Auditory System Disease 44 0.047
752
ACL001 Acalculous Cholecystitis 39 0.047
753
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.047
754
c ATM024 Autoimmune Pancreatitis 49 0.047
755
NPH003 Nephrocalcinosis 49 0.047
756
TKY002 Takayasu Arteritis 66 0.047
757
P PRG013 Paraganglioma 57 0.047
758
P NNN008 Noonan Syndrome 1 77 0.047
759
IMP005 Impotence 54 0.047
760
NDL013 Nodular Regenerative Hyperplasia 53 0.047
761
PRT029 Parathyroid Adenoma 50 0.047
762
P OBS001 Obstructive Jaundice 53 0.047
763
c PRG043 Progressive Familial Heart Block, Type Ib 40 0.047
764
FCL014 Focal Epilepsy 56 0.046
765
c ACT159 Acute Transverse Myelitis 45 0.046
766
NRL016 Neural Tube Defects 79 0.046
767
LRN003 Learning Disability 49 0.046
768
P PLZ001 Pelizaeus-Merzbacher Disease 68 0.046
769
BRN097 Brainstem Auditory Evoked Responses 24 0.046
770
PRT018 Portal Vein Thrombosis 50 0.046
771
GGN002 Gigantism 36 0.046
772
MCR191 Microscopic Colitis 50 0.046
773
P HRP009 Herpes Simplex Encephalitis 50 0.046
774
c DWL002 Dowling-Degos Disease 1 50 0.046
775
BNC003 Bone Cancer 59 0.046
776
HMP009 Haemophilus Influenzae 49 0.046
777
c ESS001 Essential Tremor 58 0.046
778
HMM003 Hemimegalencephaly 47 0.045
779
LYM052 Lymphomatoid Papulosis 45 0.045
780
NRL004 Neuroleptic Malignant Syndrome 44 0.045
781
P DDN001 Duodenal Ulcer 53 0.045
782
SXL003 Sexual Disorder 45 0.045
783
CHR005 Chorioamnionitis 52 0.045
784
P SBS003 Substance Abuse 57 0.045
785
TBC004 Tobacco Addiction 55 0.045
786
FDL002 Food Allergy 55 0.045
787
CRB085 Cerebral Hemorrhage 47 0.045
788
P ADL010 Adult Respiratory Distress Syndrome 67 0.045
789
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 37 0.045
790
LMY003 Leiomyomatosis 45 0.045
791
PRS012 Pars Planitis 48 0.045
792
P SMK004 Smoking As a Quantitative Trait Locus 3 34 0.045
793
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.045
794
CCC002 Coccidiosis 52 0.045
795
KRT001 Keratoconjunctivitis Sicca 63 0.045
796
c MCR129 Microvascular Complications of Diabetes 1 62 0.045
797
WGN006 Wegener Granulomatosis 71 0.045
798
P INT070 Intestinal Obstruction 55 0.045
799
LPR001 Lepromatous Leprosy 53 0.045
800
THR016 Thrombophlebitis 53 0.045
801
P GLM040 Glioma Susceptibility 1 51 0.044
802
VGT001 Vogt-Koyanagi-Harada Disease 60 0.044
803
HYP730 Hypogonadotropic Hypogonadism 56 0.044
804
FBR003 Fibrous Histiocytoma 46 0.044
805
c PST005 Posterior Uveitis 50 0.044
806
P LPS002 Liposarcoma 61 0.044
807
PLG002 Plague 55 0.044
808
DWR001 Dwarfism 48 0.044
809
BRW001 Brown-Vialetto-Van Laere Syndrome 27 0.044
810
YLL002 Yellow Fever 63 0.044
811
CRT016 Carotid Artery Disease 58 0.044
812
SPN029 Spondylolysis 43 0.044
813
P NMN002 Niemann-Pick Disease 68 0.044
814
LGH004 Light Chain Deposition Disease 47 0.044
815
CRB027 Cerebellar Disease 48 0.044
816
STS002 Situs Inversus 48 0.044
817
PLR008 Pleurisy 52 0.044
818
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.044
819
P LMY004 Leiomyosarcoma 59 0.044
820
TND005 Tendinitis 42 0.044
821
RTR011 Retroperitoneal Fibrosis 43 0.044
822
SMN007 Seminoma 49 0.044
823
PRT011 Protein C Deficiency 48 0.044
824
c NRF024 Neurofibromatosis, Type I 63 0.044
825
P GLL022 Guillain-Barre Syndrome 61 0.043
826
SZR001 Sezary's Disease 58 0.043
827
AMN001 Amenorrhea 55 0.043
828
P HYP083 Hypopituitarism 59 0.043
829
P CRD132 Cardiac Conduction Defect 53 0.043
830
VRN004 Vernal Keratoconjunctivitis 56 0.043
831
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.043
832
BRX001 Bruxism 51 0.043
833
VSC003 Visceral Leishmaniasis 59 0.043
834
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 0.043
835
CNR004 Cone-Rod Dystrophy 2 69 0.043
836
DSM004 Desmoid Tumor 63 0.043
837
VSC002 Vascular Dementia 58 0.043
838
ONC002 Onchocerciasis 53 0.042
839
VRC001 Varicocele 52 0.042
840
PRT038 Protein-Energy Malnutrition 52 0.042
841
OBS004 Obstructive Hydrocephalus 37 0.042
842
PLM014 Pleomorphic Adenoma 55 0.042
843
GLM008 Glomus Tumor 43 0.042
844
P CMM008 Communicating Hydrocephalus 35 0.042
845
PLV003 Pelvic Inflammatory Disease 56 0.042
846
SLV003 Salivary Gland Disease 47 0.042
847
PPL002 Papillary Carcinoma 51 0.042
848
CLR132 Colorblindness, Partial, Deutan Series 25 0.042
849
CTN007 Cutaneous Leishmaniasis 66 0.042
850
P RNL007 Renal Tubular Acidosis 51 0.042
851
PGT001 Paget's Disease of Bone 60 0.042
852
DNG002 Dengue Hemorrhagic Fever 66 0.042
853
HYD061 Hydrocephalus, Normal-Pressure 47 0.042
854
IMM001 Immune-Complex Glomerulonephritis 39 0.042
855
GNT003 Genital Herpes 58 0.042
856
DNT012 Dental Caries 50 0.042
857
AND005 Androgen Insensitivity Syndrome, Mild 16 0.042
858
CRD223 Cardiac Arrhythmia 52 0.042
859
PRN049 Paraneoplastic Pemphigus 45 0.042
860
INT002 Intermittent Claudication 61 0.042
861
DCB001 Decubitus Ulcer 44 0.042
862
c ACT210 Acute Respiratory Distress Syndrome 63 0.042
863
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.041
864
CHL004 Cholelithiasis 51 0.041
865
RFR003 Refractive Error 45 0.041
866
P RTN014 Retinal Artery Occlusion 45 0.041
867
P PLV020 Pelvic Organ Prolapse 63 0.041
868
P RSM001 Rasmussen Encephalitis 46 0.041
869
LPT001 Leptospirosis 64 0.041
870
MCL003 Macular Holes 44 0.041
871
c PSR018 Psoriasis 13 39 0.041
872
PST095 Post-Thrombotic Syndrome 52 0.041
873
SCR011 Scrapie 40 0.041
874
c MLG079 Malignant Pleural Mesothelioma 54 0.041
875
c SRC023 Sarcoidosis 2 30 0.041
876
c LSS005 Lissencephaly 1 46 0.041
877
PLS006 Plasmodium Vivax Malaria 56 0.041
878
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.041
879
P ICH004 Ichthyosis 54 0.041
880
P MMP001 Mumps 61 0.041
881
CHK001 Chikungunya 61 0.040
882
P SML001 Small Cell Carcinoma 58 0.040
883
RST023 Resting Heart Rate, Variation in 42 0.040
884
SMT003 Somatostatinoma 54 0.040
885
RGH001 Right Bundle Branch Block 44 0.040
886
PRN039 Paraneoplastic Syndromes 35 0.040
887
HPT014 Hepatorenal Syndrome 49 0.040
888
XNT003 Xanthomatosis 53 0.040
889
DCT002 Ductal Carcinoma in Situ 56 0.040
890
GNG012 Gingival Overgrowth 52 0.040
891
P FBR017 Fibrosarcoma 61 0.040
892
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 44 0.040
893
SCR001 Secretory Meningioma 41 0.040
894
c SPN393 Spinal Muscular Atrophy, Type I 50 0.040
895
BRN080 Brain Ischemia 45 0.040
896
PNM010 Pneumothorax, Primary Spontaneous 41 0.040
897
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.040
898
SPN331 Spondyloocular Syndrome 34 0.040
899
LBR002 Leber Hereditary Optic Neuropathy 57 0.040
900
PTZ001 Peutz-Jeghers Syndrome 70 0.040
901
TND006 Tendinosis 43 0.040
902
SYN058 Synucleinopathy 42 0.040
903
KLD001 Keloids 50 0.040
904
c HRD088 Hereditary Neuropathies 40 0.040
905
c SVR001 Severe Acute Respiratory Syndrome 58 0.040
906
TCK001 Tick-Borne Encephalitis 55 0.040
907
CRN024 Corneal Disease 47 0.040
908
TCL003 T Cell Deficiency 43 0.040
909
LCK001 Locked-in Syndrome 47 0.040
910
ACT055 Actinomycosis 43 0.040
911
MYC012 Mycetoma 46 0.040
912
P NML001 Nemaline Myopathy 47 0.040
913
CYS039 Cystic Kidney Disease 49 0.039
914
RBL002 Rubella Panencephalitis 13 0.039
915
HYP457 Hypertrophic Scars 48 0.039
916
PYM001 Pyomyositis 42 0.039
917
NPH018 Nephrogenic Systemic Fibrosis 56 0.039
918
PLM017 Pulmonary Alveolar Microlithiasis 48 0.039
919
CNV002 Conversion Disorder 42 0.039
920
DBT006 Diabetic Macular Edema 49 0.039
921
TXC005 Toxic Shock Syndrome 61 0.039
922
SMT001 Somatization Disorder 42 0.039
923
SPN340 Spontaneous Intracranial Hypotension 28 0.039
924
SDD008 Sudden Sensorineural Hearing Loss 46 0.039
925
ADS004 Aids Dementia Complex 42 0.039
926
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.039
927
CRV043 Cervical Dystonia 45 0.039
928
INF034 Infective Endocarditis 56 0.039
929
PLY021 Polyradiculopathy 32 0.039
930
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.039
931
LNR005 Linear Scleroderma 26 0.039
932
WLS001 Wilson Disease 72 0.039
933
LYS002 Lysosomal Storage Disease 56 0.039
934
P BLP003 Blepharospasm 46 0.039
935
TRC008 Trachoma 52 0.039
936
P TRN020 Turner Syndrome 69 0.039
937
ONC007 Oncocytoma 48 0.039
938
CYT005 Cytomegalovirus Retinitis 51 0.039
939
RSC001 Rosacea 58 0.039
940
P DYS007 Dyskeratosis Congenita 68 0.039
941
P AGN002 Agnosia 61 0.039
942
BCT004 Bacteriuria 49 0.039
943
BCL014 B-Cell Growth Factor 42 0.039
944
ACH004 Achondroplasia 67 0.039
945
HYP043 Hyperandrogenism 50 0.039
946
ELP001 Elephantiasis 40 0.039
947
TBR011 Tuberculous Meningitis 54 0.038
948
MCC002 Mucocutaneous Leishmaniasis 48 0.038
949
CHR031 Chromoblastomycosis 45 0.038
950
RCR004 Recurrent Respiratory Papillomatosis 47 0.038
951
SKL017 Skeletal Dysplasias 48 0.038
952
TRN044 Transposition of the Great Arteries 49 0.038
953
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.038
954
P CPL003 Capillary Leak Syndrome 44 0.038
955
RLP001 Relapsing Polychondritis 55 0.038
956
SPR010 Sporotrichosis 50 0.038
957
ORL013 Oral Lichen Planus 51 0.038
958
ART004 Aortic Atherosclerosis 48 0.038
959
MYT011 Myotonia 41 0.038
960
ADL030 Adult-Onset Still's Disease 65 0.038
961
ANH002 Anhidrosis 45 0.038
962
RNL078 Renal Dysplasia 49 0.038
963
PLY135 Polydactyly, Postaxial, with Progressive Myopia 30 0.037
964
ART017 Aortic Disease 57 0.037
965
NCR007 Necrotizing Fasciitis 49 0.037
966
TLN003 Telangiectasis 52 0.037
967
PRT037 Pertussis 70 0.037
968
P PLM006 Pulmonary Alveolar Proteinosis 49 0.037
969
PRP021 Peripheral Nervous System Neoplasm 53 0.037
970
BRN004 Brain Edema 57 0.037
971
c ACQ014 Acquired Hemophilia 51 0.037
972
WST001 West Syndrome 57 0.037
973
P CRN028 Corneal Ulcer 48 0.037
974
BRL010 Buruli Ulcer 51 0.037
975
ESN005 Eosinophilic Gastroenteritis 56 0.037
976
CRB011 Cerebrotendinous Xanthomatosis 64 0.037
977
P HML001 Hemolytic-Uremic Syndrome 50 0.037
978
P HYP120 Hypoaldosteronism 40 0.037
979
CHL061 Childhood Leukemia 50 0.037
980
MLT035 Multifocal Choroiditis 35 0.037
981
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 53 0.037
982
P PTY003 Pityriasis Rubra Pilaris 48 0.037
983
ACH005 Achalasia 52 0.036
984
LCH004 Lichen Disease 42 0.036
985
c ALZ056 Alzheimer Disease 3 41 0.036
986
GYN001 Gynecomastia 47 0.036
987
INF021 Infant Gynecomastia 25 0.036
988
MCK007 Muckle-Wells Syndrome 64 0.036
989
PRM042 Primary Effusion Lymphoma 61 0.036
990
PRS036 Parasitic Protozoa Infectious Disease 41 0.036
991
EXT035 Extrinsic Cardiomyopathy 33 0.036
992
P GST049 Gastrointestinal System Cancer 60 0.036
993
TRN015 Transient Cerebral Ischemia 58 0.036
994
SPR032 Superficial Siderosis of the Central Nervous System 25 0.036
995
P OST001 Osteopetrosis 70 0.036
996
PLS007 Plasmodium Falciparum Malaria 59 0.036
997
DYS011 Dyskinesia of Esophagus 39 0.036
998
P PRC019 Precocious Puberty 52 0.036
999
CNN002 Cannabis Abuse 40 0.036
1000
CYS008 Cystic Echinococcosis 47 0.036
1001
WRN003 Wernicke Encephalopathy 47 0.036
1002
THR013 Thoracic Outlet Syndrome 50 0.036
1003
HYP063 Hypersplenism 49 0.036
1004
KMR001 Kimura Disease 48 0.036
1005
P MCL013 Mucolipidosis Iv 67 0.036
1006
c CTR102 Cataract 2, Multiple Types 32 0.036
1007
OMN001 Omenn Syndrome 68 0.036
1008
DRY001 Dry Eye Syndrome 51 0.036
1009
HYP144 Hyperacusis 26 0.035
1010
P AST055 Asthma-Related Traits 1 18 0.035
1011
c PYR010 Peyronie's Disease 54 0.035
1012
STR072 Stromal Keratitis 50 0.035
1013
HYP015 Hyperlucent Lung 36 0.035
1014
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.035
1015
BCT002 Bacterial Vaginosis 56 0.035
1016
GLS018 Glass Syndrome 38 0.035
1017
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.035
1018
STT004 Steatorrhea 41 0.035
1019
IMM162 Immunoglobulin E Concentration, Serum 16 0.035
1020
OPP002 Opportunistic Mycosis 36 0.035
1021
PRM025 Primary Bacterial Infectious Disease 31 0.035
1022
GLM004 Gliomatosis Cerebri 53 0.035
1023
P FRG001 Fragile X Syndrome 69 0.035
1024
OCL008 Oculopharyngeal Muscular Dystrophy 49 0.035
1025
SVN002 Sveinsson Chorioretinal Atrophy 29 0.035
1026
P ENC008 Encephalocele 48 0.035
1027
SPH001 Sapho Syndrome 54 0.035
1028
ACR005 Acrodermatitis 35 0.035
1029
P KLP003 Klippel-Feil Syndrome 46 0.035
1030
P PSD087 Pseudoxanthoma Elasticum 67 0.035
1031
LPD009 Lipid Storage Disease 53 0.035
1032
PGM001 Pigmented Villonodular Synovitis 54 0.035
1033
ALP097 Alopecia Universalis Congenita 40 0.035
1034
TNG001 Tungiasis 40 0.035
1035
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.035
1036
PRS034 Parasitic Helminthiasis Infectious Disease 45 0.035
1037
ATX010 Ataxia Neuropathy Spectrum 29 0.035
1038
LNT002 Lentigo Maligna Melanoma 36 0.035
1039
SPN050 Spinocerebellar Degeneration 41 0.035
1040
IMM167 Immune Deficiency Disease 62 0.035
1041
MXD001 Mixed Cerebral Palsy 20 0.035
1042
AMY005 Amyloid Neuropathy 36 0.035
1043
PRN019 Perinatal Necrotizing Enterocolitis 56 0.035
1044
CWM001 Cow Milk Allergy 42 0.035
1045
ORF044 Orofacial Granulomatosis 41 0.035
1046
ANG017 Angiolipoma 36 0.035
1047
P TYS001 Tay-Sachs Disease 71 0.035
1048
TRP020 Tropical Endomyocardial Fibrosis 32 0.034
1049
DMN031 Dementia, Lewy Body 66 0.034
1050
PYR041 Pyruvate Kinase Deficiency of Red Cells 54 0.034
1051
PSD026 Pseudoainhum 26 0.034
1052
HMN009 Hemangioblastoma 56 0.034
1053
TXC020 Toxic Oil Syndrome 37 0.034
1054
HMN014 Human Immunodeficiency Virus Infectious Disease 39 0.034
1055
SPH010 Sphingolipidosis 48 0.034
1056
c ACT076 Acute Myocarditis 48 0.034
1057
ANT018 Anthracosis 39 0.034
1058
ISC002 Ischemic Optic Neuropathy 48 0.034
1059
HYD002 Hydronephrosis 49 0.034
1060
WLL006 Wells Syndrome 57 0.034
1061
CRT012 Cortical Blindness 34 0.034
1062
WRN002 Wernicke-Korsakoff Syndrome 52 0.034
1063
MYL020 Myelomeningocele 54 0.034
1064
P BRN035 Brain Stem Glioma 42 0.034
1065
MCR037 Macroglossia 44 0.034
1066
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.034
1067
LKS001 Leukostasis 39 0.034
1068
DYS016 Dysgammaglobulinemia 38 0.034
1069
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.033
1070
c DRM040 Dermatitis Herpetiformis, Familial 32 0.033
1071
INN002 Inner Ear Disease 52 0.033
1072
END041 Endometrial Adenocarcinoma 59 0.033
1073
P MCK013 Meckel Syndrome, Type 1 62 0.033
1074
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.033
1075
HPT022 Hepatoblastoma 55 0.033
1076
MLT016 Multicentric Reticulohistiocytosis 47 0.033
1077
c CRP023 Carpenter Syndrome 1 57 0.033
1078
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.033
1079
ICH054 Ichthyosis, X-Linked 59 0.033
1080
PRL013 Paralytic Poliomyelitis 28 0.033
1081
PLN005 Palindromic Rheumatism 46 0.033
1082
AKN002 Akinetic Mutism 33 0.033
1083
HYP226 Hyporeninemic Hypoaldosteronism 25 0.033
1084
ACT164 Actinic Prurigo 49 0.033
1085
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 59 0.033
1086
LYM045 Lymphocytic Vasculitis 34 0.033
1087
P PLY023 Polycystic Liver Disease 53 0.032
1088
URN003 Urinary Schistosomiasis 50 0.032
1089
MYS001 Myositis Ossificans 33 0.032
1090
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.032
1091
P ANX007 Anauxetic Dysplasia 1 36 0.032
1092