Search results for sod1

830 hits were found for sod1

# Family MCID Name MIFTS Score
1
c AMY091 Amyotrophic Lateral Sclerosis 1 87 94.092
2
P LTR001 Lateral Sclerosis 57 48.552
3
SPS236 Spastic Tetraplegia and Axial Hypotonia, Progressive 19 38.910
4
P MTR014 Motor Neuron Disease 65 36.976
5
DWN001 Down Syndrome 70 13.248
6
FRN006 Frontotemporal Dementia 68 12.639
7
P ALZ034 Alzheimer Disease 87 12.324
8
P HNT016 Huntington Disease 73 12.309
9
P NRB001 Neuroblastoma 66 12.256
10
HYP066 Hyperglycemia 60 11.896
11
ISC004 Ischemia 61 11.731
12
P DBT009 Diabetes Mellitus 67 11.454
13
c TYP009 Type 2 Diabetes Mellitus 91 11.350
14
P SPN046 Spinal Muscular Atrophy 62 11.029
15
P MLN007 Male Infertility 56 10.903
16
WLS001 Wilson Disease 70 10.699
17
P CTR002 Cataract 59 10.678
18
P KRT007 Keratoconus 49 10.546
19
BRN004 Brain Edema 54 10.471
20
P PRK057 Parkinson Disease, Late-Onset 79 10.433
21
c CHR684 Chronic Kidney Disease 73 10.414
22
P VSC007 Vascular Disease 62 10.404
23
c PRC016 Pre-Eclampsia 64 10.219
24
SNL007 Senile Cataract 40 10.169
25
LNG099 Lung Disease 62 10.107
26
MLR004 Malaria 77 10.055
27
c HYP595 Hypertension, Essential 84 10.022
28
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 9.979
29
P HRT032 Heart Disease 84 9.876
30
TNS005 Tonsillitis 57 9.876
31
P PRN023 Prion Disease 60 9.804
32
P MYP004 Myopathy 67 9.641
33
P OPN001 Open-Angle Glaucoma 55 9.288
34
P HYP097 Hyperekplexia 62 9.213
35
P RSP003 Respiratory Failure 73 9.022
36
MYL020 Myelomeningocele 51 8.847
37
P SNS001 Sensorineural Hearing Loss 60 8.825
38
P ADL010 Adult Respiratory Distress Syndrome 70 8.801
39
DFC004 Deficiency Anemia 74 8.592
40
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 8.391
41
c DLT002 Dilated Cardiomyopathy 79 8.391
42
c ATS007 Autism Spectrum Disorder 71 8.338
43
P ATS364 Autism 72 8.338
44
VRC001 Varicocele 48 8.317
45
BRN056 Bronchopulmonary Dysplasia 57 8.317
46
MNK001 Menkes Disease 64 8.295
47
P SPN301 Spinocerebellar Ataxia 2 59 8.295
48
RTN003 Retinal Ischemia 48 8.295
49
VSC002 Vascular Dementia 59 8.295
50
c HMC039 Hemochromatosis, Type 1 73 8.243
51
P RNV001 Renovascular Hypertension 48 8.210
52
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 41 8.167
53
CRB037 Cerebral Palsy 66 8.167
54
ACR006 Aceruloplasminemia 63 8.064
55
SPT006 Septooptic Dysplasia 62 8.064
56
P CNR004 Cone-Rod Dystrophy 2 74 8.064
57
P FRD001 Friedreich Ataxia 62 8.064
58
CNS004 Constipation 56 8.064
59
P CHR012 Chronic Granulomatous Disease 69 8.064
60
MLD002 Mild Pre-Eclampsia 33 8.064
61
P MTH007 Methemoglobinemia 46 8.064
62
P CRD246 Cardiovascular System Disease 55 8.064
63
MTC004 Mitochondrial Encephalomyopathy 42 8.064
64
PST030 Postcholecystectomy Syndrome 33 8.064
65
ELS001 Eales Disease 46 8.064
66
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 7.898
67
NRM005 Neuromuscular Disease 62 7.816
68
P PRP019 Peripheral Nervous System Disease 57 7.310
69
P AMY106 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia 45 7.064
70
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 64 6.964
71
P CHR071 Charcot-Marie-Tooth Disease 64 6.913
72
P SPR120 Supranuclear Palsy, Progressive, 1 68 6.844
73
c AMY023 Amyotrophic Lateral Sclerosis Type 6 36 6.728
74
PRG001 Progressive Muscular Atrophy 41 6.671
75
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 6.559
76
c AMY090 Amyotrophic Lateral Sclerosis 8 44 6.525
77
c AMY085 Amyotrophic Lateral Sclerosis 9 36 6.506
78
KR002 Kuru 45 6.486
79
MLD018 Mild Cognitive Impairment 48 6.486
80
MYC005 Myocardial Stunning 45 6.439
81
ERY004 Erysipelas 47 6.411
82
ANX004 Anoxia 40 6.103
83
HDN002 Head Injury 44 6.075
84
P RTN008 Retinitis Pigmentosa 79 6.061
85
P NRV007 Nervous System Disease 65 6.012
86
c AMY081 Amyotrophic Lateral Sclerosis Type 12 30 5.881
87
PCK003 Pick Disease of Brain 70 5.848
88
PRQ002 Paraquat Poisoning 28 5.848
89
P TTR001 Tetralogy of Fallot 69 5.805
90
c AMY059 Amyotrophic Lateral Sclerosis 19 35 5.805
91
c SPN191 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 47 5.805
92
c AMY022 Amyotrophic Lateral Sclerosis Type 5 34 5.702
93
c ALZ045 Alzheimer Disease 9 45 5.702
94
c ALZ053 Alzheimer Disease 7 33 5.702
95
ADN067 Adenoid Hypertrophy 38 5.702
96
c CRD226 Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive 48 5.702
97
P PYR039 Peyronie Disease 39 5.702
98
DMN031 Dementia, Lewy Body 65 5.702
99
PLT015 Platelet Aggregation, Spontaneous 34 5.702
100
P MPL001 Maple Syrup Urine Disease 69 5.702
101
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 49 5.702
102
P SHR029 Short Syndrome 59 5.702
103
c CNG223 Congenital Methemoglobinemia 39 5.702
104
c NRP044 Neuropathy, Hereditary Sensory and Autonomic, Type Viii 43 5.702
105
OPH001 Ophthalmomyiasis 32 5.702
106
c AMY063 Amyotrophic Lateral Sclerosis 20 31 5.702
107
c CLR106 Ciliary Dyskinesia, Primary, 26 30 5.702
108
DRM021 Dermatopathia Pigmentosa Reticularis 42 5.702
109
c SPS100 Spastic Paraplegia 38, Autosomal Dominant 38 5.702
110
P MLT008 Multinodular Goiter 41 5.702
111
CHR569 Chromosomal Duplication Syndrome 23 5.702
112
RTN001 Retinal Vasculitis 46 5.702
113
CRB027 Cerebellar Disease 47 5.702
114
c GNT045 Giant Axonal Neuropathy 2 25 5.702
115
DSS008 Disease of Mental Health 74 5.702
116
SCL003 Social Phobia 48 5.702
117
LCK001 Locked-in Syndrome 44 5.702
118
TXC002 Toxic Encephalopathy 51 5.702
119
CHR028 Chronic Wasting Disease 33 5.702
120
PRG007 Progressive Bulbar Palsy 33 5.702
121
HYP141 Hyperphenylalaninemia 42 5.702
122
MNN020 Meningococcal Infection 44 5.702
123
TTR005 Tetrahydrobiopterin Deficiency 49 5.702
124
MNN024 Meningitis and Encephalitis 27 5.702
125
P MSC003 Muscular Atrophy 52 4.192
126
P BRS047 Breast Cancer 97 3.150
127
AGN016 Aging 53 2.522
128
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.237
129
CHR178 Chromosomal Triplication 33 2.151
130
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 2.146
131
CRB004 Cerebral Artery Occlusion 45 2.088
133
SPN186 Spinal Cord Injury 60 1.957
134
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.939
135
c MCR133 Microvascular Complications of Diabetes 4 41 1.932
136
c MCR113 Microvascular Complications of Diabetes 3 52 1.932
137
c MCR130 Microvascular Complications of Diabetes 6 41 1.932
138
c MCR120 Microvascular Complications of Diabetes 7 47 1.932
139
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.867
140
P NRP001 Neuropathy 59 1.848
141
FTT001 Fatty Liver Disease 61 1.797
142
P RTN016 Retinal Degeneration 52 1.698
143
HRN029 Hearing Loss, Noise-Induced 37 1.682
144
HYP266 Hypoxia 56 1.676
145
INT002 Intermittent Claudication 61 1.623
146
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.565
147
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 1.519
148
MLT157 Multiple System Atrophy 1 69 1.456
149
P EYD002 Eye Disease 57 1.436
150
P CRD119 Cardiac Arrest 68 1.425
151
PST092 Posttransplant Acute Limbic Encephalitis 29 1.415
152
P PRK039 Parkinsonism 55 1.396
155
P DMN002 Dementia 65 1.371
156
SPS057 Spasticity 43 1.326
157
P INF038 Influenza 68 1.317
158
TRM010 Traumatic Brain Injury 50 1.317
159
P INF032 Infertility 60 1.307
160
c KRT029 Keratoconus 1 31 1.306
161
CHL014 Cholera 62 1.306
162
WLL004 Wallerian Degeneration 38 1.306
163
P MSC005 Muscular Dystrophy 66 1.298
164
c SML038 Small Cell Cancer of the Lung 68 1.291
165
P LNG032 Lung Cancer 98 1.291
166
GLB002 Glioblastoma 67 1.288
167
P HML002 Hemolytic Anemia 62 1.278
168
BRN071 Brain Injury 50 1.278
169
c ANM038 Anemia, Autoimmune Hemolytic 63 1.267
170
TXC005 Toxic Shock Syndrome 61 1.257
171
PRX085 Preaxial Hallucal Polydactyly 28 1.246
172
P LVR013 Liver Disease 68 1.246
173
NNL006 Non-Alcoholic Steatohepatitis 54 1.235
174
CLT003 Colitis 63 1.224
175
DYS073 Dysphagia 53 1.217
176
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 52 1.213
177
c GLC092 Glaucoma, Primary Open Angle 60 1.213
178
CYT002 Cytokine Deficiency 43 1.213
179
ARG004 Argyria 26 1.213
180
ATM095 Autoimmune Disease 61 1.201
181
P LPS002 Liposarcoma 64 1.193
182
P KLZ004 Kala-Azar 1 41 1.189
183
LSH001 Leishmaniasis 63 1.189
184
P THL005 Thalassemia 56 1.189
185
SKN005 Skin Atrophy 41 1.177
186
CTN007 Cutaneous Leishmaniasis 61 1.164
187
P GST053 Gastric Cancer 82 1.151
188
P ADN016 Adenocarcinoma 63 1.151
189
P PLY019 Polyneuropathy 52 1.150
190
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.137
191
SNS003 Sensory Peripheral Neuropathy 51 1.108
192
ULC004 Ulcerative Colitis 74 1.108
193
P TRM003 Tremor 50 1.107
194
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.097
195
c AMY105 Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia 34 1.078
196
ADN018 Adenoma 58 1.077
197
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.058
198
48X005 48,xyyy 39 1.034
199
TTN003 Tetanus 64 1.027
200
P BCL017 B-Cell Lymphoma 57 1.027
201
TTH006 Tooth Disease 51 1.024
202
P HYP086 Hypothyroidism 68 1.016
203
TLN003 Telangiectasis 51 1.016
204
P END044 Endometriosis 62 1.003
205
P ATX030 Ataxia-Telangiectasia 80 0.993
206
IRN002 Iron Metabolism Disease 56 0.993
207
P AMY004 Amyloidosis 69 0.993
208
P MVM001 Movement Disease 61 0.969
209
P INF037 Inflammatory Bowel Disease 53 0.957
210
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.957
211
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.957
212
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.957
213
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.957
214
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.957
215
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.957
216
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.957
217
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.957
218
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.957
219
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.957
220
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.944
221
c MJR022 Major Affective Disorder 8 37 0.944
222
P CLR023 Colorectal Cancer 100 0.944
223
c MJR024 Major Affective Disorder 9 40 0.944
224
P BPL003 Bipolar Disorder 56 0.944
225
P MLT020 Multiple Sclerosis 79 0.931
226
P NSP012 Nasopharyngeal Carcinoma 60 0.931
227
CRT072 Creutzfeldt-Jakob Disease 67 0.931
228
P HYP750 Hypertriglyceridemia, Familial 61 0.917
229
c TRM017 Tremor, Hereditary Essential, 4 35 0.917
230
GLC003 Glucose Intolerance 53 0.917
231
HYD002 Hydronephrosis 58 0.917
232
c PRG020 Paragangliomas 3 39 0.903
233
P KDN018 Kidney Disease 71 0.903
234
GLM045 Glioma 62 0.903
235
P HYP076 Hyperthyroidism 53 0.903
236
GLL048 Glial Tumor 51 0.903
237
PRT058 Pure Autonomic Failure 58 0.896
238
P GLM040 Glioma Susceptibility 1 70 0.889
239
P EPL164 Epilepsy 70 0.889
240
MNN009 Meningoencephalitis 47 0.889
241
SCR011 Scrapie 39 0.889
242
P RTN018 Retinal Disease 53 0.889
243
P DYS154 Dystonia 64 0.873
244
47X002 47,xyy 47 0.873
245
PSD088 Pseudobulbar Affect 33 0.873
246
ART140 Arteries, Anomalies of 52 0.857
247
PLY150 Polykaryocytosis Inducer 29 0.857
248
INS024 Insulin-Like Growth Factor I 77 0.857
249
LPP008 Lipoprotein Quantitative Trait Locus 65 0.857
250
P MYS005 Myositis 55 0.857
251
INC002 Inclusion Body Myositis 56 0.857
252
NRM004 Neuroma 49 0.857
253
SKN016 Skin Disease 63 0.857
254
PNG002 Pain Agnosia 51 0.841
255
P LNG064 Lung Cancer Susceptibility 3 69 0.841
257
DPR016 Depression 64 0.841
258
SPN204 Spinal Muscular Atrophy, Late-Onset, Finkel Type 29 0.823
259
P MCH002 Machado-Joseph Disease 62 0.823
260
c ACT071 Acute Kidney Failure 60 0.823
261
PLM033 Pulmonary Embolism 58 0.823
262
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.823
263
P JVN050 Juvenile Amyotrophic Lateral Sclerosis 43 0.823
264
P PNC035 Pancreatic Cancer 87 0.804
265
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.804
266
ANX010 Anxiety 70 0.804
267
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.804
268
BRN028 Brain Cancer 73 0.804
269
CRH001 Crohn's Disease 80 0.804
270
P PRG002 Progesterone-Receptor Positive Breast Cancer 33 0.804
271
CHR682 Chronic Bilirubin Encephalopathy 37 0.804
272
P SLP006 Sleep Apnea 69 0.784
273
ART002 Arts Syndrome 66 0.784
274
P LKM002 Leukemia 65 0.784
275
LVR012 Liver Cirrhosis 62 0.784
276
MDD018 Middle East Respiratory Syndrome 44 0.784
277
DMY004 Demyelinating Disease 50 0.784
278
PMP014 Pemphigoid 48 0.784
279
LWC001 Low Compliance Bladder 44 0.784
280
BLL006 Bullous Pemphigoid 61 0.784
281
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.762
282
P PHC003 Pheochromocytoma 70 0.762
283
ADR040 Adrenal Gland Pheochromocytoma 45 0.762
284
P MYS079 Miyoshi Muscular Dystrophy 53 0.762
285
LYM027 Lymphopenia 56 0.762
286
SPN022 Spinal Cord Neuroblastoma 17 0.762
287
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 40 0.750
288
P ATR011 Atrial Fibrillation 66 0.737
289
FBR054 Fibroma 44 0.737
290
P MYC007 Myocardial Infarction 69 0.737
291
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 39 0.737
292
BNR002 Bone Resorption Disease 47 0.737
293
DRG002 Drug-Induced Hepatitis 42 0.737
294
P INN002 Inner Ear Disease 49 0.737
295
P SLP005 Sleep Disorder 61 0.737
296
END086 End Stage Renal Disease 54 0.737
297
PRX035 Paroxysmal Dyskinesia 30 0.737
298
c MNS008 Monosomy 21 25 0.737
299
SDD008 Sudden Sensorineural Hearing Loss 41 0.737
300
SPS019 Spastic Paraparesis 38 0.737
301
HYP264 Hypertonia 35 0.737
302
APR001 Apraxia 51 0.709
303
P SCH015 Schizophrenia 74 0.709
304
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.709
305
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.709
306
P GRF003 Graft-Versus-Host Disease 71 0.709
307
c BTT014 Beta-Thalassemia 72 0.709
308
CRN009 Corneal Ectasia 30 0.709
309
BTT017 Beta-Thalassemia Major 54 0.709
310
MCN001 Mucinous Adenocarcinoma 49 0.709
311
APP009 Appendix Adenocarcinoma 47 0.709
312
CHR073 Choreatic Disease 53 0.709
313
NRG002 Neurogenic Bladder 54 0.709
314
c PRG011 Progressive Myoclonus Epilepsy 41 0.709
315
PRT036 Peritonitis 65 0.709
316
P CRB059 Cerebellar Degeneration 36 0.709
317
P MYC026 Myoclonus Epilepsy 35 0.709
318
P MYC033 Myoclonus 46 0.709
319
P CHR345 Chronic Pain 50 0.709
320
PRN039 Paraneoplastic Syndromes 37 0.709
321
FZL002 Fazio-Londe Disease 39 0.676
322
JPN002 Japanese Encephalitis 61 0.676
323
P AXN001 Axonal Neuropathy 33 0.676
324
P ENC004 Encephalitis 61 0.676
325
ATN005 Autonomic Dysfunction 45 0.676
326
c ATM075 Autoimmune Encephalitis 39 0.676
327
OCL015 Oculomotor Apraxia 39 0.676
328
FCL042 Facial Onset Sensory and Motor Neuronopathy 22 0.676
329
P OVR082 Overgrowth Syndrome 41 0.676
330
RTN017 Retinal Detachment 60 0.634
331
BLD131 Bladder Urothelial Carcinoma 59 0.634
332
TRT001 Teratocarcinoma 41 0.634
333
PLY021 Polyradiculopathy 33 0.634
334
CDQ001 Cauda Equina Syndrome 37 0.634
335
DBT004 Diabetic Polyneuropathy 50 0.634
336
SPN027 Spinal Stenosis 58 0.634
337
CNG506 Congenital Amyoplasia 27 0.634
338
P ENC018 Encephalopathy 62 0.567
339
LPD008 Lipid Metabolism Disorder 61 0.558
340
P HRS035 Hirschsprung Disease 1 66 0.551
341
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.551
342
TRN015 Transient Cerebral Ischemia 62 0.538
343
c ACT075 Acute Myocardial Infarction 55 0.530
344
PPL052 Papillomatosis, Confluent and Reticulated 34 0.486
345
PRP016 Paraplegia 52 0.463
346
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.451
347
P PLM037 Pulmonary Hypertension 69 0.427
348
HMN044 Human Immunodeficiency Virus Type 1 76 0.427
349
P OVR042 Ovarian Cancer 88 0.414
350
c OPT053 Optic Atrophy 1 62 0.414
351
OST159 Osteogenic Sarcoma 66 0.401
352
ATH013 Atherosclerosis Susceptibility 63 0.387
353
THR024 Thrombosis 56 0.373
354
PRM329 Premature Aging 36 0.373
355
P PRS040 Prostate Cancer 95 0.359
356
NRL016 Neural Tube Defects 80 0.359
357
MSC157 Muscular Dystrophy, Duchenne Type 78 0.359
358
c HYP836 Hypercholesterolemia, Familial, 1 73 0.359
359
NRR001 Neuroretinitis 42 0.359
360
P PNC044 Pancreatitis 61 0.359
361
RTN023 Retinitis 45 0.359
362
c DWL002 Dowling-Degos Disease 1 58 0.343
363
STR067 Stroke, Ischemic 79 0.343
364
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.343
365
CRT004 Carotid Artery Thrombosis 39 0.343
366
c ACT027 Acute Pancreatitis 60 0.343
367
MNT002 Mental Depression 56 0.343
368
P MLN008 Melanoma 75 0.343
369
STM007 Stomatitis 52 0.343
370
CRT033 Corticobasal Degeneration 48 0.343
371
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.327
372
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.327
373
P RTN024 Retinoblastoma 72 0.327
374
HMC014 Homocysteinemia 52 0.327
375
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.327
376
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.327
377
MYL069 Myeloma, Multiple 76 0.327
378
P MJR001 Major Depressive Disorder 68 0.327
379
c ATR087 Atrial Standstill 1 74 0.327
380
HYP060 Hyperinsulinism 53 0.327
381
CLN015 Colon Adenocarcinoma 64 0.327
382
c CNT035 Central Nervous System Disease 53 0.327
383
P CND004 Candidiasis 57 0.327
384
NNT024 Neonatal Stroke 31 0.327
385
c FNC027 Fanconi Anemia, Complementation Group a 80 0.311
386
c CRN221 Craniosynostosis 4 30 0.311
387
c MCR115 Microvascular Complications of Diabetes 5 65 0.311
388
P HRP006 Herpes Simplex 65 0.311
389
P HYP265 Hypotonia 42 0.311
390
BCT022 Bacterial Infectious Disease 55 0.293
391
EMB004 Embryonal Carcinoma 55 0.293
392
ALL014 Allergic Encephalomyelitis 34 0.293
393
CND006 Candida Glabrata 29 0.293
394
c HRD088 Hereditary Neuropathies 34 0.293
395
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.274
396
P OST002 Osteoporosis 76 0.274
397
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.274
398
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.274
399
P FNC044 Fanconi Anemia, Complementation Group C 56 0.274
400
CRV035 Cervical Cancer 72 0.274
401
MLG169 Malignant Astrocytoma 57 0.274
402
c HRD010 Hereditary Spastic Paraplegia 65 0.274
403
P SCK002 Sick Sinus Syndrome 55 0.274
404
P MYC008 Myocarditis 59 0.274
405
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.274
406
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.254
407
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.254
408
MSC007 Muscle Hypertrophy 64 0.254
409
c CRN216 Craniosynostosis 5 21 0.254
410
c PCH010 Pachyonychia Congenita 3 43 0.254
411
RTN020 Retinal Vascular Disease 45 0.254
412
c HPT016 Hepatitis B 62 0.254
413
GST033 Gestational Diabetes 60 0.254
414
CRY005 Cryptococcosis 61 0.254
415
DNG003 Dengue Disease 65 0.254
416
P PRD008 Periodontitis 63 0.254
417
APP008 Appendicitis 62 0.254
418
P LPS004 Lupus Erythematosus 61 0.254
419
SPN050 Spinocerebellar Degeneration 38 0.254
420
PRT251 Proteinuria, Chronic Benign 58 0.232
421
ATR057 Atrioventricular Block 54 0.232
422
PRX015 Paroxysmal Extreme Pain Disorder 56 0.232
423
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.232
424
c HPT073 Hepatitis C Virus 70 0.232
425
P SPP010 Suppressor of Tumorigenicity 3 50 0.232
426
c TYP008 Type 1 Diabetes Mellitus 77 0.232
427
CHL065 Cholangiocarcinoma 57 0.232
428
CLF027 Cleft Palate, Isolated 64 0.232
429
NND010 Nondisjunction 34 0.232
430
PRR007 Perry Syndrome 53 0.232
431
MSC190 Muscular Disease 36 0.232
432
GST023 Gastric Ulcer 52 0.232
433
OCL004 Ocular Hyperemia 24 0.232
434
HMS001 Hemosiderosis 48 0.232
435
CNG034 Congestive Heart Failure 69 0.232
436
P GST044 Gastritis 55 0.232
437
MDD011 Mood Disorder 61 0.232
438
INT079 Intrahepatic Cholangiocarcinoma 51 0.232
439
P HRD018 Hair Disease 43 0.232
440
ALL029 Allergic Disease 61 0.232
441
P UVT001 Uveitis 57 0.232
442
P ATR005 Atrophic Gastritis 50 0.232
443
DGN001 Degenerative Disc Disease 48 0.232
444
OST012 Osteoarthritis 77 0.232
445
P SCK005 Sickle Cell Disease 56 0.232
446
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.232
447
P RRH023 Rare Hereditary Hemochromatosis 52 0.232
449
c AMY088 Amyotrophic Lateral Sclerosis 3 33 0.207
450
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.207
451
MTB004 Metabolic Acidosis 48 0.207
452
RNL077 Renal Fibrosis 46 0.207
453
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.207
454
c SYS001 Systemic Lupus Erythematosus 85 0.207
455
SCH068 Schwartz-Jampel Syndrome, Type 1 52 0.207
456
c PRD040 Periodontitis, Chronic 52 0.207
457
c AMY113 Amyotrophic Lateral Sclerosis 12 with or Without Frontotemporal Dementia 27 0.207
459
c DPH024 Diaphragmatic Hernia, Congenital 63 0.207
460
IMM167 Immune Deficiency Disease 76 0.207
461
P FRG001 Fragile X Syndrome 70 0.207
462
P LKM062 Leukemia, Acute Lymphoblastic 69 0.207
463
CNG382 Congenital Cataracts, Hearing Loss, and Neurodegeneration 28 0.207
464
c KRT053 Keratoconus 7 18 0.207
465
c PRM195 Primary Lateral Sclerosis, Juvenile 35 0.207
466
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 47 0.207
467
P FTL001 Fetal Alcohol Syndrome 55 0.207
468
RBS001 Rabies 57 0.207
469
HPT019 Hepatic Encephalopathy 59 0.207
470
SQM006 Squamous Cell Carcinoma 59 0.207
471
CHL068 Cholestasis 61 0.207
472
FBR047 Fibromyalgia 57 0.207
473
P HPT021 Hepatitis 68 0.207
474
FCL012 Facial Paralysis 49 0.207
475
P PLY011 Polycystic Ovary Syndrome 57 0.207
476
c VRL010 Viral Hepatitis 52 0.207
477
P CNG001 Congenital Myasthenic Syndrome 68 0.207
478
PLS011 Plasmacytoma 56 0.207
479
QDR001 Quadriplegia 49 0.207
480
HPT004 Hepatic Coma 43 0.207
481
OCL006 Ocular Hypertension 53 0.207
482
CRT015 Carotid Artery Occlusion 45 0.207
483
GRN017 Granulocytopenia 42 0.207
484
HVY002 Heavy Metal Poisoning 22 0.207
485
CHM008 Chmp2b Frontotemporal Dementia 12 0.207
486
SPL018 Splenomegaly 47 0.207
487
c ACT134 Acute Liver Failure 57 0.207
488
ORL015 Oral Squamous Cell Carcinoma 43 0.179
489
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.179
490
CLB022 Coloboma, Ocular, Autosomal Recessive 29 0.179
491
c MGR028 Migraine with or Without Aura 1 63 0.179
492
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.179
493
P BLD134 Bladder Cancer 79 0.179
494
c EXD008 Exudative Vitreoretinopathy 1 71 0.179
495
c GLC100 Glaucoma 1, Open Angle, D 30 0.179
496
SCK003 Sickle Cell Anemia 74 0.179
497
c LKM061 Leukemia, Acute Myeloid 83 0.179
498
ANG054 Angina Pectoris 65 0.179
499
HLX001 Helix Syndrome 47 0.179
500
c AMY089 Amyotrophic Lateral Sclerosis 7 27 0.179
501
P MYC084 Mycobacterium Tuberculosis 1 68 0.179
502
P ASP006 Aspergillosis 71 0.179
503
P FTL002 Fatal Familial Insomnia 50 0.179
504
P ANP001 Anaplastic Large Cell Lymphoma 59 0.179
505
c DST106 Distal Hereditary Motor Neuronopathy Type 2 41 0.179
506
P PLY041 Polymyositis 58 0.179
507
CRY014 Cryptococcal Meningitis 48 0.179
508
P MGR003 Migraine with Aura 51 0.179
509
P CYS018 Cystitis 58 0.179
510
PST028 Post-Traumatic Stress Disorder 58 0.179
511
P GCH001 Gaucher's Disease 69 0.179
512
P BNG032 Benign Mesothelioma 53 0.179
513
CCC002 Coccidiosis 50 0.179
514
CCC001 Coccidioidomycosis 57 0.179
515
P ECL001 Eclampsia 52 0.179
516
NPH009 Nephrolithiasis 54 0.179
517
c INF023 Inflammatory Breast Carcinoma 48 0.179
518
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.179
519
ART074 Aortic Dissection 53 0.179
520
GST037 Gastroparesis 52 0.179
521
RFT001 Rift Valley Fever 50 0.179
522
P CRN025 Corneal Dystrophy 49 0.179
523
PST011 Pustulosis of Palm and Sole 52 0.179
524
LYS002 Lysosomal Storage Disease 51 0.179
525
CRN030 Coronary Stenosis 50 0.179
526
P HYP040 Hypospadias 51 0.179
527
RCK004 Rickets 64 0.179
528
MST005 Mastitis 52 0.179
529
P MGR001 Migraine Without Aura 48 0.179
530
PRM013 Premature Menopause 57 0.179
531
SCH014 Schistosomiasis 56 0.179
532
GNR004 Generalized Anxiety Disorder 54 0.179
533
P DRM010 Dermatomyositis 61 0.179
534
DYS015 Dysentery 49 0.179
535
P ART022 Arthritis 70 0.179
536
ACT084 Acute Stress Disorder 53 0.179
537
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.179
538
P LCT001 Lactic Acidosis 50 0.179
540
P PSR002 Psoriasis 63 0.179
541
APH001 Aphthous Stomatitis 57 0.179
542
CLF001 Cleft Lip 54 0.179
543
MLT075 Multifocal Motor Neuropathy 46 0.179
544
P SZR006 Seizure Disorder 69 0.179
545
CLF056 Cleft Lip with or Without Cleft Palate 43 0.179
546
C9R003 C9orf72 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 11 0.179
547
STT009 Sutton Disease 2 30 0.179
548
P PRX014 Proximal Spinal Muscular Atrophy 44 0.179
549
ACT119 Acute Promyelocytic Leukemia 62 0.146
550
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.146
551
P CRN300 Coronary Heart Disease 1 73 0.146
552
c HNT011 Huntington Disease-Like 3 33 0.146
553
P LYM118 Lymphoma 66 0.146
554
P HRD021 Hereditary Sensory Neuropathy 48 0.146
555
OCL008 Oculopharyngeal Muscular Dystrophy 52 0.146
556
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.146
557
P MRN003 Marinesco-Sjogren Syndrome 51 0.146
558
P HYP768 Hyperlipoproteinemia, Type I 67 0.146
559
P IMR002 Imerslund-Grasbeck Syndrome 1 41 0.146
560
c BRN108 Branchiootic Syndrome 1 63 0.146
561
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.146
562
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.146
563
PRP027 Peripheral Vascular Disease 71 0.146
564
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.146
565
P EXN002 Exanthem 58 0.146
566
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.146
567
c TBR025 Tuberous Sclerosis 1 84 0.146
568
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.146
569
MNN043 Meningioma, Familial 79 0.146
570
c LKM063 Leukemia, Chronic Myeloid 70 0.146
571
P HPT023 Hepatocellular Carcinoma 95 0.146
572
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.146
573
DFF005 Diffuse Large B-Cell Lymphoma 55 0.146
574
LMB062 Limb Ischemia 55 0.146
575
P ALP004 Alport Syndrome 69 0.146
576
BRR014 Barrett Esophagus 66 0.146
577
P ART021 Arteriosclerosis 53 0.146
578
P TMP001 Temporal Lobe Epilepsy 49 0.146
579
HYP014 Hyperuricemia 51 0.146
580
P TBR001 Tuberous Sclerosis 69 0.146
581
GRN055 Granular Corneal Dystrophy 36 0.146
582
P DRR001 Diarrhea 55 0.146
583
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.146
584
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.146
585
HRM003 Hormone Producing Pituitary Cancer 34 0.146
586
SVR004 Severe Combined Immunodeficiency 70 0.146
587
P PGT001 Paget's Disease of Bone 60 0.146
588
CRB033 Cerebral Degeneration 36 0.146
589
STT001 Status Epilepticus 58 0.146
590
HMP005 Hemiplegia 53 0.146
591
P ESP024 Esophagitis 60 0.146
592
PLM001 Pulmonary Tuberculosis 69 0.146
593
SCR001 Secretory Meningioma 40 0.146
594
P AGN002 Agnosia 53 0.146
595
MYF001 Myofibroma 42 0.146
596
P PTT006 Pituitary Adenoma 55 0.146
597
TST015 Testicular Disease 42 0.146
598
PLM010 Pulmonary Edema 54 0.146
599
HYP043 Hyperandrogenism 47 0.146
600
AMN003 Amnestic Disorder 53 0.146
601
PRC002 Paracoccidioidomycosis 53 0.146
602
LMY002 Leiomyoma 51 0.146
603
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.146
604
PRV004 Periventricular Leukomalacia 52 0.146
605
INT395 Intracranial Meningioma 47 0.146
606
ORL005 Oral Candidiasis 55 0.146
607
ALC010 Alcoholic Cardiomyopathy 42 0.146
608
LKS001 Leukostasis 40 0.146
609
SRC014 Sarcoma 64 0.146
610
MMM001 Mammary Paget's Disease 53 0.146
611
P MTR012 Mitral Valve Disease 57 0.146
612
P MYL006 Myeloid Leukemia 60 0.146
613
ACH005 Achalasia 54 0.146
614
c SPS092 Spastic Paraplegia 11 37 0.146
615
TXC010 Toxic Myocarditis 23 0.146
616
FND002 Fundus Dystrophy 54 0.146
617
STR019 Steroid-Induced Glaucoma 30 0.146
618
P HYP098 Hypereosinophilic Syndrome 66 0.146
619
MLG079 Malignant Pleural Mesothelioma 42 0.146
620
BCK006 Back Pain 43 0.146
621
TTR021 Tetrasomy 21 23 0.146
622
c INH030 Inherited Retinal Disorder 28 0.146
623
DSR031 Disorder of Copper Metabolism 25 0.146
624
THY029 Thyroid Carcinoma 55 0.146
625
P SCL018 Scoliosis 57 0.104
626
IDP070 Idiopathic Scoliosis 41 0.104
627
P OMP004 Omphalocele 47 0.104
628
c 3MT007 3-Methylglutaconic Aciduria 37 0.104
629
PRT082 Preterm Premature Rupture of the Membranes 56 0.104
630
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.104
631
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.104
632
P STR022 Stargardt Disease 61 0.104
633
KFR001 Kufor-Rakeb Syndrome 59 0.104
634
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.104
635
c ALZ056 Alzheimer Disease 3 56 0.104
636
MYL009 Myelodysplastic Syndrome 67 0.104
637
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.104
638
LTN004 Late-Onset Retinal Degeneration 59 0.104
639
c SPN304 Spinocerebellar Ataxia 8 47 0.104
640
TRC097 Tracheomalacia 43 0.104
641
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.104
642
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.104
643
P MDL005 Medulloblastoma 75 0.104
644
OTT002 Otitis Media 70 0.104
645
c SCH079 Schizophrenia 1 44 0.104
646
c SCL052 Scleroderma, Familial Progressive 60 0.104
647
LYM133 Lymphoma, Hodgkin, Classic 69 0.104
648
LGH007 Leigh Syndrome 70 0.104
649
P PRD006 Prader-Willi Syndrome 60 0.104
650
P CRC039 Coarctation of Aorta 46 0.104
651
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.104
652
DYN002 Doyne Honeycomb Retinal Dystrophy 44 0.104
653
SRS007 Sorsby Fundus Dystrophy 51 0.104
654
c MCP043 Mucopolysaccharidosis, Type Iiia 60 0.104
655
ALC007 Alcohol Dependence 65 0.104
656
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 31 0.104
657
INT146 Intervertebral Disc Disease 61 0.104
658
SND001 Sandhoff Disease 66 0.104
659
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.104
660
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.104
661
RST023 Resting Heart Rate, Variation in 40 0.104
662
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.104
663
HYP025 Hyperphosphatemia 47 0.104
664
P ALT001 Alternating Hemiplegia of Childhood 56 0.104
665
c BRN086 Branchiootorenal Syndrome 2 33 0.104
666
P ACN016 Acne Inversa, Familial, 3 28 0.104
667
PLY110 Polymicrogyria, Bilateral Temporooccipital 26 0.104
668
P LSS002 Lissencephaly 52 0.104
669
P BRW001 Brown-Vialetto-Van Laere Syndrome 49 0.104
670
FTL006 Fetal Alcohol Spectrum Disorder 43 0.104
671
PLY001 Polycythemia Vera 69 0.104
672
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 0.104
673
P TYS001 Tay-Sachs Disease 69 0.104
674
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.104
675
c AMY104 Amyotrophic Lateral Sclerosis 15 with or Without Frontotemporal Dementia 25 0.104
676
BRT005 Barth Syndrome 55 0.104
677
P SPR119 Spermatogenic Failure, X-Linked, 1 36 0.104
678
VTR018 Vitreoretinal Degeneration, Snowflake Type 38 0.104
679
VLV047 Volvulus of Midgut 55 0.104
680
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.104
681
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 58 0.104
682
CHR103 Charge Syndrome 65 0.104
683
CST001 Costello Syndrome 68 0.104
684
DDN011 Duodenal Atresia 47 0.104
685
ENT011 Enterocolitis 55 0.104
686
HSH003 Hashimoto Thyroiditis 60 0.104
687
KRT019 Keratitis, Hereditary 66 0.104
688
P CRP001 Carpal Tunnel Syndrome 65 0.104
689
P MYS003 Myasthenia Gravis 67 0.104
690
MYL005 Myelofibrosis 70 0.104
691
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.104
692
PHN003 Phenylketonuria 76 0.104
693
c THY056 Thyroid Dyshormonogenesis 3 32 0.104
694
c GRV008 Graves Disease 1 54 0.104
695
MND023 Mend Syndrome 49 0.104
696
TBL029 Tubulin, Beta 28 0.104
697
P STR020 Strabismus 56 0.104
698
P AST005 Asthma 75 0.104
699
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.104
700
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.104
701
c CHR660 Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a 36 0.104
702
c AMY067 Amyotrophic Lateral Sclerosis 18 34 0.104
703
c SPN255 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 5 27 0.104
704
LFR008 L-Ferritin Deficiency 19 0.104
705
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.104
706
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.104
707
c LKM070 Leukemia, Acute Monocytic 56 0.104
708
P LKM071 Leukemia, Chronic Lymphocytic 74 0.104
709
THY111 Thyroid Carcinoma, Familial Medullary 67 0.104
710
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.104
711
CHR629 Charcot-Marie-Tooth Disease and Deafness 55 0.104
712
c EXS019 Exostoses, Multiple, Type I 54 0.104
713
c MST023 Mesothelioma, Malignant 56 0.104
714
MTN003 Motion Sickness 50 0.104
715
c WLF013 Wolfram Syndrome 1 60 0.104
716
END057 Endometrial Cancer 76 0.104
717
c FRN059 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 49 0.104
718
P BND020 Bone Disease 60 0.104
719
LYM040 Lymphoblastic Lymphoma 53 0.104
720
P ANT088 Anterior Segment Dysgenesis 54 0.104
721
SPN369 Spinal Disease 43 0.104
722
P CHR084 Chromosomal Disease 35 0.104
723
INV001 Invasive Aspergillosis 48 0.104
724
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.104
725
LBR036 Leber Plus Disease 67 0.104
726
OST003 Osteonecrosis 60 0.104
727
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.104
728
P PLY014 Polycystic Kidney Disease 71 0.104
729
P SDR002 Siderosis 42 0.104
730
AMY003 Amyotrophic Neuralgia 41 0.104
731
P DDN001 Duodenal Ulcer 52 0.104
732
EXT006 Extrahepatic Cholestasis 41 0.104
733
CLN003 Clonorchiasis 42 0.104
734
DNT012 Dental Caries 53 0.104
735
PRP030 Purpura 54 0.104
736
TRN018 Transitional Cell Carcinoma 56 0.104
737
P DYS007 Dyskeratosis Congenita 66 0.104
738
P TCD001 Tic Disorder 50 0.104
739
PPL022 Papilloma 53 0.104
740
VGN023 Vaginitis 56 0.104
741
NRT004 Neuritis 53 0.104
742
IMP005 Impotence 52 0.104
743
XLN231 X-Linked Alport Syndrome 41 0.104
744
CLN044 Colon Adenoma 44 0.104
745
c CHR699 Charcot-Marie-Tooth Disease Type 2a2a 28 0.104
746
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.104
747
RCK002 Rocky Mountain Spotted Fever 34 0.104
748
ALT003 Alternating Exotropia 33 0.104
749
EXT022 Exotropia 42 0.104
750
P ALC033 Alcohol Use Disorder 67 0.104
751
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.104
752
URT010 Ureteral Obstruction 44 0.104
753
CLR030 Clear Cell Renal Cell Carcinoma 53 0.104
754
P DMY001 Demyelinating Polyneuropathy 41 0.104
755
AKN002 Akinetic Mutism 36 0.104
756
P PLY020 Polyradiculoneuropathy 47 0.104
757
SPN041 Spinal Cord Disease 54 0.104
758
ACT098 Acute Erythroid Leukemia 55 0.104
759
P CRN026 Corneal Edema 42 0.104
760
ISC001 Ischemic Neuropathy 27 0.104
761
SPS005 Spastic Hemiplegia 40 0.104
762
SQM002 Squamous Cell Papilloma 45 0.104
763
P GLM007 Glomerulonephritis 59 0.104
764
SYN007 Synovitis 54 0.104
765
PRS011 Persian Gulf Syndrome 35 0.104
766
MTS001 Mutism 44 0.104
767
P NRM006 Neuromuscular Junction Disease 34 0.104
768
END041 Endometrial Adenocarcinoma 63 0.104
769
INS001 Insulinoma 59 0.104
770
P PLM036 Pulmonary Fibrosis 65 0.104
771
THY125 Thyroid Gland Medullary Carcinoma 48 0.104
772
HGH043 High Grade Glioma 46 0.104
773
P RHB003 Rhabdomyosarcoma 66 0.104
774
c GM2006 Gm2 Gangliosidosis 46 0.104
775
P BRS044 Breast Adenocarcinoma 58 0.104
776
URM002 Uremia 47 0.104
777
P PRL003 Proliferative Glomerulonephritis 43 0.104
778
P SBS003 Substance Abuse 54 0.104
779
P HYP061 Hypertrophic Cardiomyopathy 68 0.104
780
PLC002 Plica Syndrome 35 0.104
781
ATN004 Autonomic Neuropathy 42 0.104
782
c ACT073 Acute Leukemia 59 0.104
783
c MCP001 Mucopolysaccharidosis Iii 69 0.104
784
SPT005 Spotted Fever 49 0.104
785
ACS001 Acoustic Neuroma 55 0.104
786
P GLL022 Guillain-Barre Syndrome 59 0.104
787
MGS001 Megaesophagus 44 0.104
788
BTT018 Beta-Thalassemia Intermedia 31 0.104
789
CHG001 Chagas Disease 65 0.104
790
P NTR004 Neutropenia 62 0.104
791
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.104
792
AZS001 Azoospermia 45 0.104
793
MLL002 Miller Fisher Syndrome 40 0.104
794
PRT037 Pertussis 49 0.104
795
P OPT009 Optic Neuritis 57 0.104
796
GT001 Gout 63 0.104
797
P INT070 Intestinal Obstruction 57 0.104
798
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.104
799
P MST009 Mastocytosis 64 0.104
800
CHL061 Childhood Leukemia 47 0.104
801
P VSC011 Vasculitis 61 0.104
802
ALL006 Allergic Asthma 55 0.104
803
LRN003 Learning Disability 49 0.104
804
DYS032 Dystrophinopathies 47 0.104
805
HPP002 Huppke-Brendel Syndrome 7 0.104
806
ACT200 Acute Monoblastic Leukemia 40 0.104
807
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.104
808
PRP007 Priapism 46 0.104
809
MCH006 Mechanical Strabismus 40 0.104
810
P PLY018 Polycythemia 56 0.104
811
P MNC007 Monocytic Leukemia 48 0.104
812
CHR066 Chronic Fatigue Syndrome 59 0.104
813
HRD016 Hereditary Retinal Dystrophy 33 0.104
814
P DST101 Distal Hereditary Motor Neuropathies 23 0.104
815
ATP014 Atp8b1 Deficiency 28 0.104
816
P THY032 Thyroiditis 56 0.104
817
P VTR008 Vitreoretinal Degeneration 30 0.104
818
DFF036 Differentiated Thyroid Carcinoma 51 0.104
819
OVR094 Ovarian Epithelial Cancer 39 0.104
820
INF041 Infantile-Onset Ascending Hereditary Spastic Paralysis 30 0.104
821
LNP001 Loin Pain Hematuria Syndrome 17 0.104
822
HYP056 Hypoglycemia 65 0.104
823
FNG016 Fungal Keratitis 40 0.104
824
BNG077 Benign Idiopathic Neonatal Seizures 23 0.104
825
CHR233 Chromosome 21q Deletion 12 0.104
826
DWR001 Dwarfism 44 0.104
827
P GNG009 Gangliosidosis 44 0.104
828
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.104
829
SPS188 Spastic Paraplegia-Paget Disease of Bone Syndrome 25 0.104
830
CRD137 Cardiogenic Shock 56 0.104
Content
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