Search results for chronic progressive multiple sclerosis

1493 hits were found for chronic progressive multiple sclerosis

# Family MCID Name MIFTS Score
1
c SCN036 Secondary Progressive Multiple Sclerosis 49 4.101
2
P LKM002 Leukemia 71 0.519
3
P HPT021 Hepatitis 69 0.472
4
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.442
5
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.432
6
P LTR001 Lateral Sclerosis 53 0.428
7
DMY004 Demyelinating Disease 53 0.417
8
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.414
9
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.387
10
P MLT019 Multiple Myeloma 83 0.370
11
c CHR090 Chronic Lymphocytic Leukemia 76 0.366
12
ATM052 Autoimmune Disease 1 25 0.352
13
ATM053 Autoimmune Disease 2 16 0.348
14
P KDN018 Kidney Disease 66 0.328
15
c MLT093 Multiple Sclerosis 2 18 0.326
16
c HPT001 Hepatitis C 68 0.322
17
P TBR001 Tuberous Sclerosis 67 0.307
18
ATM054 Autoimmune Disease 3 15 0.299
19
LNG099 Lung Disease 64 0.294
20
c ATM007 Autoimmune Disease of Central Nervous System 25 0.293
21
c MLT094 Multiple Sclerosis 3 24 0.281
22
P LYM118 Lymphoma 69 0.281
23
NRN002 Neuronitis 41 0.270
24
PRS047 Prostatitis 56 0.268
25
c HPT016 Hepatitis B 64 0.263
26
P PNC044 Pancreatitis 61 0.260
27
P CHR345 Chronic Pain 50 0.257
28
ATM055 Autoimmune Disease 4 15 0.254
29
P MYL006 Myeloid Leukemia 66 0.253
30
NRM005 Neuromuscular Disease 56 0.245
31
BLD054 Blood Protein Disease 37 0.245
32
END072 Endotheliitis 42 0.239
33
P LVR013 Liver Disease 75 0.238
34
CRB009 Cerebritis 39 0.236
35
P EPL164 Epilepsy 66 0.234
36
c MLT095 Multiple Sclerosis 4 16 0.232
37
MLT021 Multiple System Atrophy 70 0.232
38
P MYP004 Myopathy 67 0.231
39
P NRV007 Nervous System Disease 71 0.231
40
P ART022 Arthritis 75 0.231
41
SPN369 Spinal Disease 39 0.229
42
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.229
43
PRP027 Peripheral Vascular Disease 68 0.225
44
VSC006 Vascular Cancer 51 0.225
45
ATM059 Autoimmune Disease 6 22 0.223
46
c HPT073 Hepatitis C Virus 73 0.222
47
P PRM108 Primary Progressive Multiple Sclerosis 46 0.220
48
SPS057 Spasticity 42 0.220
49
RSP006 Respiratory System Disease 58 0.216
50
P BLD051 Blood Coagulation Disease 42 0.216
51
PLS009 Plasma Cell Neoplasm 48 0.215
52
VSC008 Vascular Hemostatic Disease 30 0.212
53
P VNS003 Venous Insufficiency 54 0.211
54
MRG013 Mirage Syndrome 29 0.210
55
c PND001 Pain Disorder 54 0.210
56
DMN002 Dementia 65 0.207
57
P NRP001 Neuropathy 59 0.204
58
c VRL010 Viral Hepatitis 60 0.204
59
CRD118 Cardiovascular Cancer 44 0.203
60
P HMR003 Hemorrhagic Disease 57 0.203
61
SPN041 Spinal Cord Disease 51 0.199
62
PRP019 Peripheral Nervous System Disease 55 0.199
63
P MSC033 Muscle Disorders 52 0.197
64
c MLT124 Multiple Sclerosis 5 23 0.197
65
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.196
66
P BRS047 Breast Cancer 100 0.195
67
ATN002 Autonomic Nervous System Disease 48 0.195
68
NTR005 Nutritional Deficiency Disease 36 0.195
69
ATM012 Autoimmune Disease of Blood 35 0.195
70
P HRT032 Heart Disease 75 0.194
71
MSC004 Muscle Tissue Disease 34 0.193
72
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.193
73
ALR002 Al-Raqad Syndrome 36 0.192
74
P THY032 Thyroiditis 54 0.191
75
c HPT003 Hepatitis a 59 0.190
76
SKN016 Skin Disease 66 0.190
77
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.189
78
P HPT023 Hepatocellular Carcinoma 92 0.188
79
P CRV039 Cervicitis 45 0.186
80
P PLM037 Pulmonary Hypertension 79 0.186
81
MTR014 Motor Neuron Disease 58 0.186
82
INC022 Inclusion-Cell Disease 46 0.186
83
c CHR418 Chronic Leukemia 47 0.185
84
PRP021 Peripheral Nervous System Neoplasm 46 0.184
85
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.183
86
P NRV006 Nervous System Cancer 60 0.183
87
IMP003 Impaired Renal Function Disease 34 0.183
88
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.181
89
CNN005 Connective Tissue Disease 62 0.181
90
P PRS040 Prostate Cancer 90 0.179
91
P ENC018 Encephalopathy 59 0.179
92
c CHR089 Chronic Kidney Failure 66 0.178
93
BNM001 Bone Marrow Cancer 51 0.176
94
BNS002 Bone Structure Disease 37 0.176
95
C3D001 C3 Deficiency 53 0.176
96
P LYM033 Lymphoproliferative Syndrome 56 0.176
97
P GLM007 Glomerulonephritis 59 0.175
98
IMM136 Immune System Disease 51 0.175
99
RTN023 Retinitis 50 0.173
100
P RHM011 Rheumatoid Arthritis 89 0.173
101
MTH009 Mouth Disease 61 0.173
102
ACD009 Acid-Labile Subunit, Deficiency of 45 0.172
103
P AST005 Asthma 82 0.171
104
HMT002 Hematologic Cancer 64 0.170
105
P ADN016 Adenocarcinoma 69 0.170
106
P PRD008 Periodontitis 63 0.170
107
P PLY019 Polyneuropathy 56 0.170
108
SKN027 Skin Conditions 43 0.168
109
c CHR417 Chronic Graft Versus Host Disease 51 0.168
110
MVM001 Movement Disease 49 0.167
111
P LYM026 Lymphoblastic Leukemia 62 0.167
112
P MLT074 Multiple Endocrine Neoplasia 56 0.166
113
LRN003 Learning Disability 49 0.166
114
NRT004 Neuritis 52 0.165
115
VRL011 Viral Infectious Disease 55 0.165
116
MLN008 Melanoma 62 0.165
117
PCK002 Pick Disease 68 0.164
118
URN009 Urinary System Disease 50 0.163
119
HMT018 Hematopoietic Stem Cell Transplantation 41 0.163
120
PRM243 Primary Bone Cancer 29 0.163
121
P PNM007 Pneumonia 68 0.163
122
OPT009 Optic Neuritis 50 0.162
123
P URF003 Urofacial Syndrome 1 50 0.161
124
P LPS004 Lupus Erythematosus 64 0.161
125
LYM023 Lymphatic System Cancer 33 0.161
126
CHR066 Chronic Fatigue Syndrome 64 0.160
127
LYM024 Lymphatic System Disease 52 0.160
128
c CNT035 Central Nervous System Disease 60 0.159
129
PHY002 Physical Disorder 43 0.159
130
BNC003 Bone Cancer 58 0.159
131
ANR040 Aneurysm 57 0.156
132
PDT025 Pediatric Multiple Sclerosis 36 0.155
133
BLD053 Blood Platelet Disease 46 0.155
134
P BCL006 B-Cell Lymphomas 65 0.153
135
ATH003 Atherosclerosis 65 0.152
136
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.152
137
BRT030 Birth Defects 43 0.151
138
LYM067 Lymphoid Leukemia 44 0.151
139
SLP005 Sleep Disorder 53 0.151
140
ALN001 Aland Island Eye Disease 45 0.150
141
ADJ001 Adjustment Disorder 38 0.149
142
ACR041 Acromelic Frontonasal Dysostosis 45 0.149
143
HDC001 Headache 54 0.148
144
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.147
145
SQM006 Squamous Cell Carcinoma 70 0.147
146
P AST007 Astrocytoma 65 0.147
147
CNG034 Congestive Heart Failure 72 0.146
148
P RSP003 Respiratory Failure 71 0.145
149
ISC004 Ischemia 61 0.144
150
P CRB088 Cerebral Atrophy 42 0.144
151
BCK006 Back Pain 43 0.144
152
P NRM001 Neuromyelitis Optica 60 0.143
153
OCL009 Ocular Cancer 59 0.143
154
WTH001 Withdrawal Disorder 37 0.143
155
STR067 Stroke, Ischemic 75 0.142
156
P SPS003 Spastic Diplegia 52 0.141
157
END030 End Stage Renal Failure 55 0.141
158
PRG090 Progressive Relapsing Multiple Sclerosis 30 0.140
159
OPT006 Optic Nerve Disease 52 0.140
160
P ATX004 Ataxia 53 0.140
161
FST001 Foster-Kennedy Syndrome 31 0.138
162
VSC007 Vascular Disease 67 0.137
163
BRN028 Brain Cancer 70 0.136
164
P GLM045 Glioma 60 0.136
165
PRD011 Proud Syndrome 42 0.136
166
LPD004 Lipoid Nephrosis 48 0.135
167
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.135
168
SKN023 Skin Tag 44 0.135
169
VSC009 Vascular Skin Disease 19 0.134
170
ATN003 Autonomic Nervous System Neoplasm 40 0.134
171
P PLM036 Pulmonary Fibrosis 71 0.134
172
ADM013 Adamantinoma of Long Bones 57 0.133
173
P RNL014 Renal Cell Carcinoma 82 0.133
174
P KDN017 Kidney Cancer 65 0.133
175
c SYS001 Systemic Lupus Erythematosus 86 0.132
176
P DMY001 Demyelinating Polyneuropathy 43 0.132
177
P MSC003 Muscular Atrophy 50 0.132
178
INT066 Interstitial Lung Disease 59 0.131
179
LKC003 Leukocyte Disease 43 0.131
180
HYP266 Hypoxia 56 0.131
181
GLC077 Glucocorticoid Therapy, Response to 16 0.131
182
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.131
183
VND001 Vein Disease 47 0.130
184
APH002 Aphasia 54 0.130
185
P MNN013 Meningitis 67 0.130
186
HV1006 Hiv-1 80 0.129
187
P ART023 Arthropathy 64 0.129
188
P ESP024 Esophagitis 61 0.129
189
P CRD011 Cardiomyopathy 68 0.128
190
P SYS005 Systemic Scleroderma 61 0.128
191
DSS008 Disease of Mental Health 52 0.128
192
c AST037 Asthma 1 28 0.127
193
OTT002 Otitis Media 66 0.127
194
c CRN214 Coronary Heart Disease 5 22 0.127
195
P ENC004 Encephalitis 63 0.126
196
P OBS005 Obesity 92 0.126
197
c AST039 Asthma 2 28 0.126
198
P SCH015 Schizophrenia 77 0.126
199
ADN018 Adenoma 58 0.125
200
LYM019 Lymphosarcoma 53 0.125
201
DFF003 Diffuse Scleroderma 41 0.125
202
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.125
203
c ADL001 Adult Lymphoma 39 0.124
204
P PNC035 Pancreatic Cancer 87 0.124
205
P CRN178 Coronary Heart Disease 6 21 0.124
206
URT039 Urticaria 57 0.123
207
P INF038 Influenza 72 0.123
208
SRC014 Sarcoma 66 0.123
209
GLB003 Globe Disease 32 0.123
210
ADT003 Auditory System Disease 40 0.123
211
P CRN211 Coronary Artery Disease 74 0.123
212
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.122
213
THR024 Thrombosis 57 0.122
214
P MYC007 Myocardial Infarction 79 0.122
215
MYL031 Myeloproliferative Neoplasm 58 0.121
216
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.120
217
c CHR064 Chronic Monocytic Leukemia 42 0.120
218
P GST044 Gastritis 56 0.120
219
ART111 Artery Disease 55 0.120
220
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.120
221
P AMY004 Amyloidosis 65 0.120
222
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.119
223
VSC011 Vasculitis 62 0.119
224
CTS003 Coats Disease 57 0.119
225
PLY020 Polyradiculoneuropathy 45 0.118
226
ATN005 Autonomic Dysfunction 49 0.117
227
DFC004 Deficiency Anemia 64 0.117
228
CSY001 C Syndrome 50 0.117
229
RHM027 Rheumatic Disease 58 0.117
230
P HYP069 Hyperparathyroidism 58 0.117
231
MNT002 Mental Depression 53 0.116
232
ALL026 Allergic Hypersensitivity Disease 52 0.115
233
c HYP595 Hypertension, Essential 69 0.115
234
ADR009 Adrenal Cortex Disease 39 0.115
235
ANX002 Anxiety Disorder 67 0.115
236
P CHR562 Chronic Myelocytic Leukemia 41 0.115
237
CNS004 Constipation 57 0.115
238
MDD011 Mood Disorder 61 0.114
239
PRT036 Peritonitis 63 0.114
240
LVR012 Liver Cirrhosis 67 0.114
241
c CHR431 Chronic Venous Insufficiency 44 0.114
242
P ALZ034 Alzheimer Disease 92 0.113
243
KDS001 Kid Syndrome 53 0.113
244
c DYS119 Dystonia 9 36 0.113
245
P CRN035 Cranial Nerve Palsy 46 0.113
246
NWC001 Newcastle Disease 54 0.113
247
CLT003 Colitis 60 0.113
248
c TRC078 Trichohepatoenteric Syndrome 2 29 0.112
249
CHL071 Child Syndrome 58 0.112
250
P PSR002 Psoriasis 61 0.112
251
NSD001 Nose Disease 48 0.112
252
FRB001 Farber Lipogranulomatosis 53 0.111
253
ADL002 Adult Syndrome 52 0.111
254
GLC008 Glucose Metabolism Disease 42 0.111
255
DRM006 Dermatitis 66 0.111
256
CNT010 Central Nervous System Hematologic Cancer 18 0.111
257
SPC010 Speech and Communication Disorders 41 0.110
258
BRN071 Brain Injury 52 0.110
259
END040 Endogenous Depression 53 0.110
260
P THR014 Thrombocytopenia 64 0.110
261
CLC006 Calcinosis 50 0.110
262
GLT021 Glutaricaciduria, Type I 46 0.110
263
WLL006 Wells Syndrome 59 0.110
264
c ACT073 Acute Leukemia 60 0.109
265
ART021 Arteriosclerosis 58 0.109
266
OST017 Osteomyelitis 61 0.109
267
LPD008 Lipid Metabolism Disorder 58 0.108
268
ATR060 Atrial Standstill, Digenic 51 0.108
269
GNG013 Gingivitis 61 0.107
270
ALL014 Allergic Encephalomyelitis 32 0.107
271
c CRN175 Coronary Heart Disease 4 19 0.107
272
TBR010 Tuberculosis 70 0.107
273
HDG012 Hodgkin Lymphoma 77 0.106
274
RTN018 Retinal Disease 53 0.106
275
EXF001 Exfoliation Syndrome 57 0.106
276
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.106
277
P PLN008 Peeling Skin Syndrome 45 0.106
278
TTH006 Tooth Disease 52 0.105
279
c CRN172 Coronary Heart Disease 3 19 0.105
280
ISC006 Ischemic Heart Disease 68 0.105
281
SPN186 Spinal Cord Injury 63 0.105
282
GDS001 Good Syndrome 44 0.105
283
PRP030 Purpura 58 0.105
284
GNR004 Generalized Anxiety Disorder 51 0.104
285
P CND004 Candidiasis 57 0.104
286
SXL003 Sexual Disorder 42 0.104
287
P DRR001 Diarrhea 60 0.104
288
P OST012 Osteoarthritis 83 0.103
289
ANG018 Angiomyolipoma 46 0.103
290
P MDL005 Medulloblastoma 77 0.103
291
P UVT001 Uveitis 58 0.103
292
ACQ007 Acquired Immunodeficiency Syndrome 60 0.102
293
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 42 0.102
294
P PRS038 Personality Disorder 62 0.101
295
TMP001 Temporal Lobe Epilepsy 50 0.101
296
MYC033 Myoclonus 42 0.101
297
AYM001 Ayme-Gripp Syndrome 41 0.101
298
P MSC005 Muscular Dystrophy 65 0.101
299
JNT002 Joint Disorders 55 0.101
300
CHL068 Cholestasis 59 0.100
301
PRD007 Periodontal Disease 60 0.100
302
BLD044 Bladder Disease 51 0.100
303
AND005 Androgen Insensitivity Syndrome, Mild 16 0.100
304
c INT072 Intestinal Pseudo-Obstruction 46 0.100
305
P PYL005 Pyelonephritis 52 0.099
306
EWN003 Ewing Sarcoma 66 0.099
307
c CRN174 Coronary Heart Disease 2 20 0.099
308
DYS073 Dysphagia 48 0.098
309
CND002 Conduct Disorder 54 0.098
310
EYD002 Eye Disease 61 0.098
311
P CLL015 Collagen Disease 50 0.098
312
P TRM003 Tremor 54 0.098
313
CRN031 Cranial Nerve Disease 40 0.097
314
P INF037 Inflammatory Bowel Disease 63 0.097
315
c CRN173 Coronary Heart Disease 8 18 0.097
316
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.096
317
P INF032 Infertility 59 0.096
318
CRB039 Cerebrovascular Disease 63 0.096
319
P PLY014 Polycystic Kidney Disease 53 0.096
320
GST050 Gastrointestinal System Disease 56 0.096
321
RDN001 Reading Disorder 34 0.096
322
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.096
323
NRN004 Neuroendocrine Tumor 56 0.096
324
c CLL013 Cell Type Cancer 46 0.096
325
FSC004 Fasciitis 48 0.095
326
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.095
327
P TCL004 T-Cell Leukemia 47 0.095
328
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.095
329
TST021 Testicular Germ Cell Tumor 69 0.094
330
P NTR004 Neutropenia 59 0.094
331
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.094
332
PRM097 Primary Immunodeficiency Disease 60 0.093
333
ETH011 Ethylmalonic Encephalopathy 56 0.093
334
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.093
335
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.093
336
VSC047 Vascular Malformation 45 0.093
337
SPC003 Specific Developmental Disorder 38 0.093
338
P LYM007 Lymphangioleiomyomatosis 66 0.093
339
P NRF002 Neurofibromatosis 71 0.093
340
P GLB002 Glioblastoma 68 0.092
341
HPT074 Hepatic Adenoma, Somatic 50 0.092
342
P SPN046 Spinal Muscular Atrophy 65 0.091
343
SNS023 Sensory System Cancer 43 0.091
344
P LRY019 Laryngitis 54 0.090
345
STM006 Stomach Disease 50 0.090
346
CNT098 Central Core Disease 65 0.090
347
ATP002 Atopy 66 0.090
348
P DYS154 Dystonia 65 0.090
349
c PRM092 Primary Lateral Sclerosis, Adult, 1 29 0.090
350
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.089
351
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.089
352
P MYL005 Myelofibrosis 67 0.089
353
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.089
354
INS024 Insulin-Like Growth Factor I 75 0.089
355
P RPD001 Rapidly Progressive Glomerulonephritis 45 0.088
356
HRT007 Heart Cancer 46 0.088
357
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.088
358
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.087
359
DDN006 Duodenitis 42 0.087
360
PRS042 Prostate Disease 52 0.087
361
HNM002 Hinman Syndrome 25 0.087
362
PRM025 Primary Bacterial Infectious Disease 41 0.087
363
P HRT017 Heart Tumor 32 0.086
364
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.086
365
GRM001 Germ Cell and Embryonal Cancer 36 0.086
366
SYS003 Systolic Heart Failure 43 0.086
367
CHR008 Choroiditis 44 0.086
368
MYL001 Myelitis 51 0.086
369
P SZR006 Seizure Disorder 56 0.086
370
P FLL037 Follicular Lymphoma 70 0.086
371
P CHR084 Chromosomal Disease 32 0.085
372
MCR004 Macroglobulinemia 50 0.085
373
P ACT074 Acute Lymphocytic Leukemia 56 0.085
374
P NPH012 Nephrotic Syndrome 59 0.085
375
ACT049 Acute Disseminated Encephalomyelitis 49 0.085
376
P PRK057 Parkinson Disease, Late-Onset 70 0.085
377
P CTR002 Cataract 58 0.085
378
SPS019 Spastic Paraparesis 41 0.084
379
ACR002 Acrocapitofemoral Dysplasia 33 0.084
380
BND014 Bone Development Disease 40 0.084
381
DFF005 Diffuse Large B-Cell Lymphoma 59 0.084
382
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.084
383
c CNT068 Central Pain Syndrome 29 0.084
384
c ADL079 Adult Heart Tumor 16 0.084
385
P RNL015 Renal Hypertension 48 0.084
386
P NRB001 Neuroblastoma 70 0.084
387
P HML002 Hemolytic Anemia 62 0.083
388
LPM005 Lipomatosis 47 0.083
389
P INT068 Intestinal Disease 60 0.083
390
c RNL016 Renal Infectious Disease 20 0.083
391
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.082
392
CRB037 Cerebral Palsy 66 0.082
393
P INT001 Intrahepatic Cholestasis 59 0.082
394
P OST002 Osteoporosis 64 0.082
395
PRP016 Paraplegia 49 0.082
396
P PRM006 Primary Biliary Cirrhosis 51 0.082
397
BRC012 Brucellosis 66 0.082
398
CRH001 Crohn's Disease 75 0.082
399
P SKN013 Skin Benign Neoplasm 43 0.082
400
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.082
401
ULC004 Ulcerative Colitis 76 0.082
402
c MLT010 Multiple Personality Disorder 36 0.082
403
c ADL017 Adult T-Cell Leukemia 60 0.081
404
P CRB042 Cerebellar Ataxia 63 0.081
405
HML018 Homologous Wasting Disease 13 0.081
406
TRG002 Trigeminal Neuralgia 57 0.081
407
c PLN018 Peeling Skin Syndrome 2 40 0.081
408
FXF002 Fox-Fordyce Disease 36 0.081
409
P HYD006 Hydrocephalus 66 0.081
410
BSL008 Basal Ganglia Disease 40 0.080
411
PNC034 Pancreas Disease 58 0.080
412
c PNC106 Pancreatic Agenesis 1 37 0.080
413
ART016 Aortic Aneurysm 69 0.080
414
P GT001 Gout 58 0.080
415
ACT118 Acute Non Lymphoblastic Leukemia 30 0.080
416
c HMG001 Hemoglobin C Disease 47 0.080
417
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.080
418
PSY004 Psychotic Disorder 67 0.079
419
P HYP086 Hypothyroidism 64 0.079
420
HDN002 Head Injury 45 0.079
421
ARC002 Arachnoiditis 41 0.079
422
HYP264 Hypertonia 39 0.079
423
GLM004 Gliomatosis Cerebri 49 0.079
424
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.079
425
c PRG001 Progressive Muscular Atrophy 39 0.078
426
P SLP006 Sleep Apnea 61 0.078
427
ANG054 Angina Pectoris 50 0.078
428
P RCK004 Rickets 61 0.078
429
ANG049 Angioedema Induced by Ace Inhibitors 34 0.077
430
PLM031 Poliomyelitis 60 0.077
431
HYP066 Hyperglycemia 61 0.077
432
FCL011 Facial Nerve Disease 36 0.077
433
GNC005 Geniculate Ganglionitis 27 0.077
434
P GST049 Gastrointestinal System Cancer 60 0.077
435
GNG011 Gingival Disease 46 0.077
436
c MTR002 Mitral Valve Insufficiency 44 0.077
437
c LKM061 Leukemia, Acute Myeloid 73 0.077
438
APR001 Apraxia 51 0.076
439
RNL097 Renal Artery Disease 43 0.076
440
ATM013 Autoimmune Disease of Cardiovascular System 13 0.076
441
PRP080 Peripheral Artery Disease 37 0.076
442
P GNT008 Giant Cell Tumor 49 0.076
443
DRG001 Drug Psychosis 38 0.076
444
CNV002 Conversion Disorder 41 0.076
445
c PLN017 Peeling Skin Syndrome 1 34 0.076
446
BRN106 Burns 52 0.075
447
MXD023 Mixed Cell Type Cancer 44 0.075
448
P FNC043 Fanconi Anemia, Complementation Group E 55 0.075
449
P MYS003 Myasthenia Gravis 67 0.075
450
P OLG002 Oligodendroglioma 56 0.075
451
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.075
452
P CNN004 Connective Tissue Cancer 40 0.075
453
c CNG031 Congenital Nervous System Abnormality 37 0.074
454
c LKM062 Leukemia, Acute Lymphoblastic 64 0.074
455
P MYS005 Myositis 57 0.074
456
P MCR129 Microvascular Complications of Diabetes 1 54 0.074
457
c PLN021 Peeling Skin Syndrome 3 29 0.074
458
c LYM107 Lymphoproliferative Syndrome 2 50 0.074
459
SBS003 Substance Abuse 54 0.074
460
P HNT016 Huntington Disease 80 0.074
461
P DRM010 Dermatomyositis 62 0.074
462
ETN001 Eating Disorder 58 0.074
463
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.073
464
P HRP006 Herpes Simplex 65 0.073
465
P SHR029 Short Syndrome 58 0.073
466
PLM034 Pulmonary Emphysema 55 0.073
467
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.072
468
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.072
469
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.072
470
BHR001 Behr Syndrome 42 0.072
471
CRB033 Cerebral Degeneration 44 0.072
472
ALP008 Alopecia 57 0.072
473
FML039 Female Reproductive System Disease 48 0.072
474
NSY001 N Syndrome 36 0.072
475
SPN051 Spondylitis 51 0.071
476
OCL006 Ocular Hypertension 48 0.071
477
RST001 Restless Legs Syndrome 54 0.071
478
c LYM106 Lymphoproliferative Syndrome 1 32 0.071
479
WST001 West Syndrome 57 0.071
480
MYC002 Mycobacterium Avium Complex Disease 52 0.071
481
GST092 Gastroesophageal Reflux 62 0.071
482
P CNJ013 Conjunctivitis 64 0.071
483
TXC002 Toxic Encephalopathy 51 0.071
484
P LYM025 Lymphedema 61 0.071
485
SPC005 Speech Disorder 41 0.071
486
KRT002 Keratomalacia 52 0.071
487
GLB015 Glioblastoma Multiforme 63 0.071
488
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.071
489
SNS003 Sensory Peripheral Neuropathy 45 0.071
490
ADR007 Adrenoleukodystrophy 72 0.071
491
P PRT013 Portal Hypertension 60 0.071
492
P TRC086 Trichohepatoenteric Syndrome 1 48 0.071
493
VTM003 Vitamin Metabolic Disorder 30 0.071
494
CLN019 Colonic Disease 51 0.070
495
c ATS347 Autosomal Dominant Polycystic Kidney Disease 62 0.070
496
TRM010 Traumatic Brain Injury 52 0.070
497
CRY004 Cryoglobulinemia 46 0.070
498
GST019 Gastrointestinal Stromal Tumor 73 0.070
499
P ESN008 Eosinophilic Pneumonia 51 0.070
500
P TRN034 Transverse Myelitis 49 0.070
501
MDS022 Mediastinitis 41 0.070
502
c CRN176 Coronary Heart Disease 9 18 0.070
503
P CNT005 Central Nervous System Lymphoma 53 0.070
504
P MYC008 Myocarditis 54 0.070
505
P DYS021 Dysautonomia 44 0.070
506
P PLY041 Polymyositis 52 0.070
507
PHR003 Pharyngitis 56 0.070
508
c PSR017 Psoriasis 2 37 0.070
509
P MTC069 Mitochondrial Disorders 53 0.069
510
ADR038 Adermatoglyphia 46 0.069
511
P ALX003 Alexander Disease 63 0.069
512
PNN001 Panniculitis 51 0.069
513
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.069
514
c ATM011 Autoimmune Hepatitis 60 0.069
515
CHL067 Cholecystitis 57 0.069
516
OCL011 Ocular Motility Disease 37 0.069
517
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.069
518
P ALC004 Alcohol Abuse 59 0.068
519
SWL001 Swallowing Disorders 33 0.068
520
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.068
521
P HST010 Histiocytosis 58 0.068
522
LYM017 Lyme Disease 63 0.068
523
P HYP098 Hypereosinophilic Syndrome 63 0.068
524
CHG001 Chagas Disease 67 0.068
525
P ACT135 Acute Graft Versus Host Disease 53 0.068
526
CRB025 Carbohydrate Metabolic Disorder 46 0.068
527
c ACT075 Acute Myocardial Infarction 60 0.067
528
MND006 Mondor Disease 21 0.067
529
PRC013 Pericarditis 51 0.067
530
c ACT071 Acute Kidney Failure 49 0.067
531
MGR028 Migraine with or Without Aura 1 47 0.067
532
SNS001 Sensorineural Hearing Loss 57 0.067
533
BRD001 Brody Myopathy 47 0.067
534
RNL077 Renal Fibrosis 47 0.067
535
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.067
536
c LCL006 Localized Scleroderma 61 0.066
537
INT253 Intestinal Benign Neoplasm 47 0.066
538
CRB031 Cerebral Arterial Disease 27 0.066
539
CRN030 Coronary Stenosis 51 0.066
540
LPM004 Lipoma 60 0.066
541
c CRN177 Coronary Heart Disease 7 20 0.066
542
DBT010 Diabetic Neuropathy 55 0.066
543
P CHR071 Charcot-Marie-Tooth Disease 67 0.066
544
SXD001 Sex Differentiation Disease 38 0.066
545
c DLT002 Dilated Cardiomyopathy 76 0.066
546
MYC006 Mycosis Fungoides 66 0.066
547
c NRF018 Neurofibromatosis, Type 1 67 0.065
548
CNN002 Cannabis Abuse 40 0.065
549
DSC009 Discoid Lupus Erythematosus 45 0.065
550
MSL001 Measles 61 0.065
551
TRP002 Tropical Spastic Paraparesis 55 0.065
552
P RTN016 Retinal Degeneration 54 0.065
553
P LKD001 Leukodystrophy 59 0.065
554
THY028 Thyroid Cancer 69 0.064
555
GLB001 Gilbert Syndrome 60 0.064
556
MXD005 Mixed Connective Tissue Disease 62 0.064
557
CPL005 Capillary Disease 36 0.064
558
URM002 Uremia 48 0.064
559
P PRP029 Porphyria 59 0.064
560
SNG003 Single Ventricular Heart 22 0.064
561
c FLL041 Follicular Lymphoma 1 45 0.064
562
CLS010 Cluster Headache 44 0.064
563
SYN007 Synovitis 58 0.064
564
P INT063 Intellectual Disability 49 0.064
565
c FML303 Familial/multiple Cancer 14 0.064
566
P HMC003 Hemochromatosis 72 0.063
567
KRN002 Kearns-Sayre Syndrome 61 0.063
568
CRB002 Cerebral Primitive Neuroectodermal Tumor 41 0.063
569
BRN002 Bronchiolitis 56 0.063
570
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.063
571
P HYP265 Hypotonia 38 0.063
572
KRT004 Keratitis 71 0.063
573
CRB027 Cerebellar Disease 47 0.063
574
SPN040 Spinal Cancer 39 0.063
575
GST045 Gastroenteritis 59 0.063
576
P END044 Endometriosis 66 0.063
577
MNR003 Mineral Metabolism Disease 38 0.063
578
CRS005 Crest Syndrome 51 0.063
579
FBR012 Fabry Disease 69 0.063
580
ART017 Aortic Disease 57 0.063
581
c PRK031 Parkinson Disease 1 51 0.063
582
END035 Endocrine Gland Cancer 49 0.063
583
ATR076 Atrophic Muscular Disease 15 0.062
584
BNM008 Bone Mineral Density, Low 16 0.062
585
c CHR579 Chiari Malformation Type Ii 37 0.062
586
P HMN010 Hemangioma 59 0.062
587
THR004 Thrombocytosis 55 0.062
588
c PRM226 Primary Central Nervous System Lymphoma 49 0.062
589
P RBL001 Rubella 57 0.062
590
HRP004 Herpes Zoster 56 0.062
591
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.062
592
PRP036 Peripheral T-Cell Lymphoma 45 0.062
593
IRN001 Iron Deficiency Anemia 52 0.062
594
LYM027 Lymphopenia 56 0.062
595
c CNN010 Connective Tissue Benign Neoplasm 32 0.062
596
P ATP001 Atopic Dermatitis 62 0.062
597
c ACT020 Acute T Cell Leukemia 35 0.061
598
NSP002 Nasopharyngitis 40 0.061
599
P PLY018 Polycythemia 58 0.061
600
CHL123 Chlamydia 60 0.061
601
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.061
602
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.061
603
OBS061 Obstructive Sleep Apnea 66 0.061
604
c PRG106 Progressive Muscular Dystrophy 40 0.061
605
TCL003 T Cell Deficiency 45 0.061
606
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.061
607
BNF002 Bone Fracture 50 0.061
608
ESP023 Esophageal Disease 54 0.061
609
HRY003 Hairy Cell Leukemia 57 0.061
610
FTD001 Foot Drop 33 0.061
611
c DLT001 Delta Chain Disease 13 0.061
612
P MST009 Mastocytosis 56 0.061
613
SCH014 Schistosomiasis 58 0.060
614
P SPN052 Spondyloarthropathy 60 0.060
615
P BPL003 Bipolar Disorder 62 0.060
616
CRC006 Carcinoid Syndrome 52 0.060
617
c NRM008 Neuromyelitis Optica Spectrum Disorder 27 0.060
618
P HYP060 Hyperinsulinism 58 0.060
619
P CRT072 Creutzfeldt-Jakob Disease 61 0.060
620
HYP056 Hypoglycemia 61 0.060
621
P APL001 Aplastic Anemia 75 0.060
622
PRS063 Paresthesia 36 0.060
623
LMB062 Limb Ischemia 48 0.060
624
OLV001 Olivopontocerebellar Atrophy 53 0.060
625
INS001 Insulinoma 61 0.059
626
GRN017 Granulocytopenia 44 0.059
627
TCD001 Tic Disorder 48 0.059
628
P EHL001 Ehlers-Danlos Syndrome 63 0.059
629
c ACT027 Acute Pancreatitis 57 0.059
630
c OPT055 Optic Atrophy Plus Syndrome 52 0.059
631
P END033 Endocarditis 54 0.059
632
SML033 Small Cell Cancer of the Lung, Somatic 54 0.059
633
ATM014 Autoimmune Disease of Endocrine System 36 0.059
634
UPP004 Upper Respiratory Tract Disease 46 0.059
635
AMN002 Amino Acid Metabolic Disorder 47 0.059
636
ATM016 Autoimmune Disease of Skin and Connective Tissue 29 0.059
637
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.059
638
PST028 Post-Traumatic Stress Disorder 57 0.059
639
NRF007 Neurofibroma 53 0.059
640
P CLC005 Celiac Disease 68 0.059
641
GRW007 Growth Hormone Deficiency 50 0.059
642
MLT075 Multifocal Motor Neuropathy 41 0.059
643
P HMP007 Hemophilia 57 0.059
644
c INH020 Inherited Metabolic Disorder 49 0.059
645
P SYR001 Syringomyelia 47 0.059
646
PRR002 Pure Red-Cell Aplasia 47 0.059
647
P FML035 Familial Hyperlipidemia 48 0.059
648
ESN015 Eosinophilic Fasciitis 47 0.059
649
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.059
650
QFV001 Q Fever 60 0.058
651
PLM033 Pulmonary Embolism 60 0.058
652
P GNR027 Generalized Peeling Skin Syndrome 19 0.058
653
BRN012 Bronchiolitis Obliterans 58 0.058
654
GST023 Gastric Ulcer 56 0.058
655
EYC003 Eye Accommodation Disease 24 0.058
656
DRG003 Drug Dependence 50 0.058
657
KWS002 Kawasaki Disease 70 0.058
658
P AGG001 Aggressive Periodontitis 50 0.058
659
PSR001 Psoriatic Arthritis 64 0.058
660
TND004 Tendinopathy 42 0.058
661
c MYC058 Myocardial Infarction 2 28 0.058
662
BCL002 B Cell Deficiency 49 0.058
663
PRT011 Protein C Deficiency 52 0.058
664
TTN003 Tetanus 61 0.057
665
CRT016 Carotid Artery Disease 57 0.057
666
CNT018 Central Nervous System Leukemia 37 0.057
667
CYT008 Cytomegalovirus Infection 52 0.057
668
PLM010 Pulmonary Edema 54 0.057
669
CLC001 Calciphylaxis 46 0.057
670
RNL011 Renal Osteodystrophy 45 0.057
671
NRR001 Neuroretinitis 42 0.057
672
CRS001 Crescentic Glomerulonephritis 42 0.057
673
DVL001 Developmental Coordination Disorder 36 0.057
674
HMP005 Hemiplegia 51 0.057
675
OBS002 Obsessive-Compulsive Disorder 66 0.057
676
ATN004 Autonomic Neuropathy 45 0.057
677
EYD001 Eye Degenerative Disease 30 0.057
678
P PLY017 Polyarteritis Nodosa 51 0.057
679
MLR004 Malaria 83 0.057
680
P LPR003 Leprosy 69 0.057
681
MNN017 Mononeuropathy 40 0.057
682
c OST147 Osteoarthritis 1 30 0.057
683
P FCL005 Focal Segmental Glomerulosclerosis 60 0.057
684
P EPN002 Ependymoma 53 0.056
685
P INT030 Intracranial Aneurysm 54 0.056
686
c THR092 Thrombophilia Due to Thrombin Defect 54 0.056
687
PLM001 Pulmonary Tuberculosis 67 0.056
688
HYP037 Hyperhomocysteinemia 50 0.056
689
P CRB059 Cerebellar Degeneration 34 0.056
690
P SYP003 Syphilis 53 0.056
691
SPT004 Septic Arthritis 60 0.056
692
CHL061 Childhood Leukemia 49 0.056
693
c CNT015 Central Sleep Apnea 44 0.056
694
P FML187 Familial Hypertension 38 0.056
695
P ART084 Arteriovenous Fistula 44 0.055
696
PMS001 Poems Syndrome 52 0.055
697
PST046 Post-Transplant Lymphoproliferative Disease 54 0.055
698
P SPR098 Supranuclear Palsy, Progressive 56 0.055
699
P SML001 Small Cell Carcinoma 56 0.055
700
P NSP012 Nasopharyngeal Carcinoma 66 0.055
701
DST006 Diastolic Heart Failure 46 0.055
702
RFR010 Refractory Anemia 45 0.055
703
P SDR002 Siderosis 44 0.055
704
PLM012 Pulmonary Sarcoidosis 54 0.055
705
PNM008 Pneumothorax 53 0.055
706
P ANT006 Antiphospholipid Syndrome 56 0.055
707
P MYP006 Myopia 56 0.055
708
c MLG068 Malignant Glioma 51 0.055
709
c SML023 Small Cell Lung Cancer, Adult 15 0.055
710
ZLL002 Zollinger-Ellison Syndrome 53 0.055
711
MSC072 Muscle Cancer 49 0.055
712
P CMR001 Camurati-Engelmann Disease 58 0.054
713
c MLT136 Multiple Endocrine Neoplasia 1 69 0.054
714
ABL002 Ablepharon-Macrostomia Syndrome 57 0.054
715
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.054
716
LYM127 Lymphatic Malformations 39 0.054
717
P PRM016 Primary Optic Atrophy 29 0.054
718
PLS010 Plasma Protein Metabolism Disease 34 0.054
719
BLL006 Bullous Pemphigoid 59 0.054
720
PRC012 Pericardial Effusion 51 0.054
721
RCT018 Rectal Neoplasm 54 0.054
722
P EXN002 Exanthem 57 0.054
723
PNC119 Pancreatic Neuroendocrine Tumor 40 0.054
724
TRN018 Transitional Cell Carcinoma 53 0.054
725
GLC003 Glucose Intolerance 55 0.054
726
P INT070 Intestinal Obstruction 57 0.054
727
VTM002 Vitamin B12 Deficiency 44 0.054
728
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.053
729
c HMG004 Hemoglobin D Disease 31 0.053
730
P HYP024 Hypoparathyroidism 53 0.053
731
STT001 Status Epilepticus 59 0.053
732
DCH001 Duchenne Muscular Dystrophy 79 0.053
733
PYD001 Pyoderma Gangrenosum 51 0.053
734
P MTC003 Metachromatic Leukodystrophy 70 0.053
735
INT042 Internuclear Ophthalmoplegia 37 0.053
736
ACT084 Acute Stress Disorder 40 0.053
737
P PRP003 Porphyria Cutanea Tarda 64 0.053
738
P DBT005 Diabetes Insipidus 53 0.053
739
PYD002 Pyoderma 48 0.053
740
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.053
741
P GRV001 Graves' Disease 59 0.053
742
RBR001 Roberts Syndrome 60 0.053
743
PLY023 Polycystic Liver Disease 56 0.053
744
P ANP001 Anaplastic Large Cell Lymphoma 57 0.053
745
CNT047 Contact Dermatitis 61 0.052
746
LSH001 Leishmaniasis 66 0.052
747
DWN001 Down Syndrome 66 0.052
748
MTR007 Motor Peripheral Neuropathy 37 0.052
749
HYP020 Hyperprolactinemia 60 0.052
750
CRB085 Cerebral Hemorrhage 46 0.052
751
LNS003 Lens Disease 33 0.052
752
P PNC001 Pancytopenia 52 0.052
753
LMY002 Leiomyoma 54 0.052
754
DCB001 Decubitus Ulcer 41 0.051
755
P MCR010 Microcephaly 58 0.051
756
IRR002 Irritable Bowel Syndrome 58 0.051
757
P FNC004 Fanconi Syndrome 49 0.051
758
OST003 Osteonecrosis 45 0.051
759
c ACT134 Acute Liver Failure 50 0.051
760
P NRC002 Narcolepsy 62 0.051
761
c MLT009 Multiple Cranial Nerve Palsy 33 0.051
762
GST040 Gastric Adenocarcinoma 52 0.051
763
ARC007 Arachnoid Cysts 39 0.051
764
PTT006 Pituitary Adenoma 56 0.051
765
NRS005 Neurosarcoidosis 23 0.051
766
BNN003 Bone Inflammation Disease 44 0.051
767
URN008 Urinary Bladder Cancer 66 0.051
768
LYM116 Lymph Node Disease 47 0.051
769
c DYS033 Dysautonomia Like Disorder 16 0.051
770
CRB086 Cerebral Aneurysms 39 0.050
771
FBR054 Fibroma 46 0.050
772
PPL022 Papilloma 55 0.050
773
THY030 Thyroid Gland Disease 48 0.050
774
HYP068 Hyperostosis 40 0.050
775
STM007 Stomatitis 50 0.050
776
FDL002 Food Allergy 53 0.050
777
c MCL042 Macular Degeneration, Age-Related, 1 73 0.050
778
c INF071 Inflammatory Bowel Disease 1 51 0.050
779
c SYS004 Systemic Mastocytosis 60 0.050
780
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.050
781
P DDN001 Duodenal Ulcer 50 0.050
782
CD4004 Cd4 Deficiency 14 0.050
783
BRN080 Brain Ischemia 41 0.050
784
TST014 Testicular Cancer 53 0.050
785
c SRC025 Sarcoidosis 1 61 0.050
786
CMM004 Common Variable Immunodeficiency 68 0.050
787
ISL001 Islet Cell Tumor 50 0.050
788
c ANT034 Anterior Uveitis 48 0.049
789
MNN009 Meningoencephalitis 47 0.049
790
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.049
791
VSL005 Visual Pathway Disease 29 0.049
792
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.049
793
CNT067 Central Cord Syndrome 23 0.049
794
P LCH002 Lichen Planus 53 0.049
795
GST030 Gastrinoma 42 0.049
796
INT007 Intermediate Coronary Syndrome 50 0.049
797
P HYP607 Hypercholesterolemia, Familial 76 0.049
798
HRT029 Heart Tumor of the Child 15 0.049
799
MRK001 Merkel Cell Carcinoma 52 0.049
800
GNG002 Ganglioneuroma 47 0.049
801
P CLR108 Colorectal Adenoma 60 0.049
802
WBR001 Weber Syndrome 41 0.049
803
CRD001 Cardiac Tamponade 44 0.049
804
INT075 Intracranial Hypertension 50 0.049
805
c MCR115 Microvascular Complications of Diabetes 5 57 0.049
806
MLG088 Malignant Germ Cell Tumor 38 0.049
807
P XLN007 X-Linked Disease 34 0.049
808
HRT012 Heart Valve Disease 40 0.048
809
MRF001 Marfan Syndrome 73 0.048
810
PRN023 Prion Disease 48 0.048
811
P MYT002 Myotonic Dystrophy 48 0.048
812
P MSC007 Muscle Hypertrophy 58 0.048
813
ATN001 Autonomic Peripheral Neuropathy 17 0.048
814
WLL001 Williams-Beuren Syndrome 60 0.048
815
PLN006 Poland Syndrome 54 0.048
816
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.048
817
VSL004 Visual Cortex Disease 28 0.048
818
P TXP001 Toxoplasmosis 61 0.048
819
P KRT007 Keratoconus 48 0.048
820
c ATM089 Autoimmune Neuropathy 26 0.048
821
c OPT053 Optic Atrophy 1 43 0.048
822
ANG037 Angiomatosis 37 0.048
823
P AXN001 Axonal Neuropathy 38 0.048
824
PRC002 Paracoccidioidomycosis 55 0.048
825
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.048
826
c ESS001 Essential Tremor 59 0.048
827
CHR001 Churg-Strauss Syndrome 49 0.048
828
VSC001 Vascular Myelopathy 23 0.048
829
P TRT010 Teratoma 52 0.048
830
P PRL003 Proliferative Glomerulonephritis 43 0.048
831
SFT003 Soft Tissue Sarcoma 57 0.047
832
c INF078 Inflammatory Bowel Disease 2 31 0.047
833
ASP003 Aseptic Meningitis 51 0.047
834
P PNM006 Pneumoconiosis 51 0.047
835
P NPH009 Nephrolithiasis 60 0.047
836
ALX002 Alexithymia 37 0.047
837
ANG020 Angiosarcoma 53 0.047
838
NCR004 Nocardiosis 43 0.047
839
SCK005 Sickle Cell Disease 51 0.047
840
SMT001 Somatization Disorder 42 0.047
841
PHT003 Phototoxic Dermatitis 35 0.047
842
OST011 Osteomalacia 49 0.047
843
DND018 Dendritic Cell Tumor 41 0.047
844
ADP007 Adie Pupil 34 0.047
845
c MNN043 Meningioma, Familial 59 0.047
846
INC002 Inclusion Body Myositis 66 0.047
847
CRB040 Cerebrum Cancer 32 0.047
848
c ATM075 Autoimmune Encephalitis 38 0.047
849
PRS039 Prostate Adenocarcinoma 46 0.047
850
QDR001 Quadriplegia 52 0.046
851
TTR016 Tetra-Amelia Syndrome 36 0.046
852
SPN020 Spondylosis 48 0.046
853
HMS001 Hemosiderosis 46 0.046
854
P CTN003 Cutaneous Lupus Erythematosus 48 0.046
855
NRM004 Neuroma 48 0.046
856
PRN011 Pernicious Anemia 44 0.046
857
c SRC023 Sarcoidosis 2 33 0.046
858
ACR007 Acromegaly 66 0.046
859
c CHR576 Chronic Beryllium Disease 41 0.046
860
CLR030 Clear Cell Renal Cell Carcinoma 53 0.046
861
CHN016 Cohen Syndrome 54 0.046
862
CRB004 Cerebral Artery Occlusion 45 0.046
863
RNL101 Renal Cell Carcinoma, Papillary 63 0.046
864
P HYP076 Hyperthyroidism 55 0.046
865
IRN002 Iron Metabolism Disease 41 0.046
866
BRN069 Brain and Spinal Tumors 12 0.046
867
FCL003 Facial Hemiatrophy 30 0.045
868
P ATS007 Autism Spectrum Disorder 65 0.045
869
P LPD010 Lipodystrophy 55 0.045
870
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.045
871
CRT049 Critical Limb Ischemia 51 0.045
872
CRD119 Cardiac Arrest 61 0.045
873
FCT008 Factitious Disorder 41 0.045
874
HYP085 Hypothalamic Disease 44 0.045
875
c VRL007 Viral Encephalitis 54 0.045
876
WLL004 Wallerian Degeneration 36 0.045
877
WRN001 Werner Syndrome 67 0.045
878
SRT004 Serotonin Syndrome 49 0.045
879
HDR003 Hidradenitis 45 0.045
880
HST009 Histiocytoma 47 0.045
881
PRT029 Parathyroid Adenoma 48 0.045
882
c PRK045 Parkinson Disease 5 40 0.045
883
CHR072 Chordoma 61 0.045
884
MSS002 Mass Syndrome 48 0.045
885
VST004 Vestibular Disease 44 0.045
886
P THR015 Thrombophilia 59 0.044
887
SPR066 Superficial Siderosis 34 0.044
888
MGC001 Megacolon 45 0.044
889
c DRR009 Diarrhea 6 29 0.044
890
BTN003 Biotinidase Deficiency 57 0.044
891
FLR002 Filariasis 54 0.044
892
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.044
893
PPL021 Papilledema 47 0.044
894
ACN011 Acne 62 0.044
895
TRY001 Trypanosomiasis 51 0.044
896
P RTN022 Retinal Vein Occlusion 38 0.044
897
EPS006 Epstein Syndrome 38 0.044
898
MTC056 Mitochondrial Dna Depletion Syndrome 4a 48 0.044
899
LCH009 Lichen Sclerosus 41 0.044
900
P LGH007 Leigh Syndrome 70 0.044
901
PRT018 Portal Vein Thrombosis 49 0.044
902
HDR002 Hidradenitis Suppurativa 51 0.043
903
P SCL009 Sclerosing Cholangitis 48 0.043
904
SLP001 Sleeping Sickness 48 0.043
905
GRD007 Grade Iii Astrocytoma 50 0.043
906
CCN007 Cocoon Syndrome 45 0.043
907
c BRN108 Branchiootic Syndrome 1 34 0.043
908
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.043
909
P LMY004 Leiomyosarcoma 55 0.043
910
c PST005 Posterior Uveitis 46 0.043
911
ART012 Aortitis 30 0.043
912
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.043
913
FNC002 Functional Diarrhea 37 0.043
914
SPR008 Supratentorial Primitive Neuroectodermal Tumor 42 0.043
915
P ALP009 Alopecia Areata 62 0.043
916
GNG004 Ganglioglioma 50 0.043
917
RHB003 Rhabdomyosarcoma 57 0.042
918
BRN018 Borna Disease 42 0.042
919
MMB001 Membranoproliferative Glomerulonephritis 46 0.042
920
c HMP029 Hemophilia a 63 0.042
921
c ATM022 Autoimmune Myocarditis 42 0.042
922
P IDP010 Idiopathic Generalized Epilepsy 61 0.042
923
MXD032 Mixed Germ Cell Tumor 34 0.042
924
ADR012 Adrenal Gland Disease 48 0.042
925
PRT014 Protein S Deficiency 53 0.042
926
P ADD001 Addison's Disease 62 0.042
927
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.042
928
ALC006 Alcoholic Hepatitis 59 0.042
929
IMP005 Impotence 51 0.042
930
DPH001 Diphtheria 59 0.042
931
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.042
932
DWR001 Dwarfism 47 0.042
933
ACL001 Acalculous Cholecystitis 35 0.042
934
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.042
935
INT051 Intussusception 50 0.042
936
RTN001 Retinal Vasculitis 44 0.042
937
CLL021 Collagenous Colitis 39 0.041
938
OBS001 Obstructive Jaundice 48 0.041
939
GGN002 Gigantism 32 0.041
940
P MCH002 Machado-Joseph Disease 63 0.041
941
MDD010 Middle Ear Disease 48 0.041
942
THR016 Thrombophlebitis 53 0.041
943
ERY003 Erythema Multiforme 55 0.041
944
LRG008 Large Granular Lymphocyte Leukemia 39 0.041
945
KPS004 Kaposi Sarcoma 67 0.041
946
P HVY001 Heavy Chain Disease 41 0.041
947
P GRN010 Granular Cell Tumor 47 0.041
948
TNG004 Tongue Disease 39 0.041
949
CRB159 Cerebral Visual Impairment 33 0.041
950
MTC005 Mitochondrial Metabolism Disease 36 0.041
951
ATS008 Autosomal Dominant Disease 39 0.041
952
P STR020 Strabismus 51 0.041
953
CGL001 Coagulation Protein Disease 14 0.041
954
LMY003 Leiomyomatosis 42 0.041
955
HNS001 Hansen's Disease 30 0.041
956
NPH003 Nephrocalcinosis 48 0.041
957
P ATX010 Ataxia Neuropathy Spectrum 30 0.041
958
STF001 Stiff-Person Syndrome 56 0.041
959
P FML011 Familial Adenomatous Polyposis 68 0.041
960
NPH010 Nephrosclerosis 43 0.041
961
P ORT004 Orthostatic Intolerance 64 0.041
962
P SML016 Small Intestine Cancer 52 0.041
963
P CMM008 Communicating Hydrocephalus 36 0.041
964
c ALZ012 Alzheimer Disease 12 32 0.041
965
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.041
966
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.041
967
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.041
968
CRY005 Cryptococcosis 50 0.040
969
PTZ001 Peutz-Jeghers Syndrome 71 0.040
970
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.040
971
FNC006 Functional Gastric Disease 32 0.040
972
LYM021 Lymphadenitis 58 0.040
973
KDN015 Kidney Angiomyolipoma 41 0.040
974
MST019 Mastoiditis 32 0.040
975
CNT046 Central Nervous System Vasculitis 46 0.040
976
MCR088 Microscopic Polyangiitis 49 0.040
977
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.040
978
RHM028 Rheumatic Heart Disease 50 0.040
979
FBR009 Fibrous Dysplasia 45 0.040
980
c INF086 Inflammatory Bowel Disease 3 38 0.040
981
P HRP009 Herpes Simplex Encephalitis 47 0.040
982
SPN029 Spondylolysis 39 0.040
983
FBR003 Fibrous Histiocytoma 43 0.040
984
TND005 Tendinitis 39 0.040
985
c HYP615 Hyperparathyroidism, Familial Primary 56 0.040
986
P RTT002 Rett Syndrome 77 0.040
987
PPT005 Peptic Ulcer Disease 58 0.040
988
VSC002 Vascular Dementia 54 0.040
989
MXD025 Mixed Germ Cell Cancer 31 0.040
990
WSC001 Wisconsin Syndrome 14 0.040
991
SPN027 Spinal Stenosis 55 0.040
992
DCT002 Ductal Carcinoma in Situ 51 0.040
993
ANS012 Anus Disease 32 0.040
994
PLG002 Plague 51 0.040
995
RTN020 Retinal Vascular Disease 48 0.040
996
PPL002 Papillary Carcinoma 51 0.040
997
P ICH004 Ichthyosis 52 0.040
998
c HRD088 Hereditary Neuropathies 40 0.039
999
NRM002 Normal Pressure Hydrocephalus 50 0.039
1000
P LPS002 Liposarcoma 55 0.039
1001
HMM003 Hemimegalencephaly 45 0.039
1002
RNL007 Renal Tubular Acidosis 50 0.039
1003
P DNT015 Dent Disease 61 0.039
1004
TXC005 Toxic Shock Syndrome 60 0.039
1005
SMN007 Seminoma 45 0.039
1006
c PRK022 Parkinson Disease 12 21 0.039
1007
NRS003 Neurosyphilis 41 0.039
1008
CNR002 Cone-Rod Dystrophy 64 0.039
1009
INF013 Inferior Myocardial Infarction 35 0.039
1010
BRN097 Brainstem Auditory Evoked Responses 22 0.039
1011
PRS012 Pars Planitis 43 0.039
1012
IMG001 Image Syndrome 50 0.039
1013
CVT001 Cavitary Optic Disc Anomalies 31 0.039
1014
LMB024 Limbic Encephalitis 38 0.039
1015
YNG002 Young Syndrome 26 0.039
1016
NCR007 Necrotizing Fasciitis 46 0.039
1017
CLD014 Cole Disease 37 0.039
1018
P SHR001 Short Bowel Syndrome 49 0.038
1019
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.038
1020
SMT003 Somatostatinoma 48 0.038
1021
HMP009 Haemophilus Influenzae 45 0.038
1022
RMS001 Rem Sleep Behavior Disorder 41 0.038
1023
c PRK025 Parkinson Disease 10 38 0.038
1024
KRT006 Keratoconjunctivitis 52 0.038
1025
CHL004 Cholelithiasis 48 0.038
1026
P HML001 Hemolytic-Uremic Syndrome 51 0.038
1027
MCL027 Macular Dystrophy, Dominant Cystoid 36 0.038
1028
P CRD132 Cardiac Conduction Defect 43 0.038
1029
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.038
1030
PRX075 Proximal Myopathy and Ophthalmoplegia 41 0.038
1031
c NRF019 Neurofibromatosis, Type 2 62 0.038
1032
P HYP083 Hypopituitarism 54 0.038
1033
SLV003 Salivary Gland Disease 47 0.038
1034
LYM022 Lymphangioma 54 0.038
1035
ANG011 Angiodysplasia 44 0.038
1036
PRN039 Paraneoplastic Syndromes 32 0.038
1037
PLM014 Pleomorphic Adenoma 52 0.038
1038
RCT015 Reactive Arthritis 63 0.038
1039
LYM008 Lymphangiosarcoma 47 0.037
1040
P SCL015 Scleritis 49 0.037
1041
MTS001 Mutism 43 0.037
1042
PTT009 Pituitary Gland Disease 47 0.037
1043
P LNG064 Lung Cancer Susceptibility 3 62 0.037
1044
GLM008 Glomus Tumor 42 0.037
1045
LYM052 Lymphomatoid Papulosis 41 0.037
1046
INF034 Infective Endocarditis 51 0.037
1047
GLC036 Glucagonoma 46 0.037
1048
LPT001 Leptospirosis 62 0.037
1049
ENG004 Engraftment Syndrome 32 0.037
1050
P PLM040 Pulmonary Valve Disease 43 0.037
1051
CLL003 Cellulitis 51 0.037
1052
P HYP237 Hypercalcemia, Infantile 47 0.037
1053
PTH002 Pathological Gambling 51 0.037
1054
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.037
1055
ART004 Aortic Atherosclerosis 46 0.037
1056
RNL078 Renal Dysplasia 45 0.037
1057
RFR003 Refractive Error 43 0.037
1058
NRL004 Neuroleptic Malignant Syndrome 41 0.037
1059
STS002 Situs Inversus 46 0.037
1060
MCL003 Macular Holes 41 0.037
1061
c DSB006 Desbuquois Dysplasia 1 50 0.037
1062
RLP003 Relapsing Fever 45 0.037
1063
FNC005 Functional Colonic Disease 27 0.037
1064
TRN044 Transposition of the Great Arteries 48 0.037
1065
P HYP117 Hypertriglyceridemia 61 0.037
1066
CRH005 Crohn's Colitis 52 0.037
1067
SPH001 Sapho Syndrome 46 0.037
1068
PRS036 Parasitic Protozoa Infectious Disease 41 0.036
1069
RTR011 Retroperitoneal Fibrosis 39 0.036
1070
CHR005 Chorioamnionitis 48 0.036
1071
NDL013 Nodular Regenerative Hyperplasia 50 0.036
1072
LPD009 Lipid Storage Disease 49 0.036
1073
P WSK001 Wiskott-Aldrich Syndrome 73 0.036
1074
SPS007 Spastic Cerebral Palsy 44 0.036
1075
DNT012 Dental Caries 46 0.036
1076
VNT001 Ventilation Pneumonitis 35 0.036
1077
WRT002 Writing Disorder 27 0.036
1078
ERD001 Erdheim-Chester Disease 52 0.036
1079
c CLL012 Cell Type Benign Neoplasm 39 0.036
1080
LGH004 Light Chain Deposition Disease 44 0.036
1081
HPY002 H. Pylori Infection 61 0.036
1082
SKN005 Skin Atrophy 40 0.036
1083
P FRG001 Fragile X Syndrome 69 0.036
1084
IRS003 Iris Disease 31 0.036
1085
VRC001 Varicocele 51 0.036
1086
AMN001 Amenorrhea 50 0.036
1087
HYP540 Hypertension, Diastolic 39 0.036
1088
ORL014 Oral Pharyngeal Disorders 11 0.036