Search results for SOD1

284 hits were found for SOD1

# Family MCID Name MIFTS Score
1
SPS236 Spastic Tetraplegia and Axial Hypotonia, Progressive 16 10.335
2
c AMY091 Amyotrophic Lateral Sclerosis 1 89 6.919
3
P LTR001 Lateral Sclerosis 54 5.878
4
P MTR014 Motor Neuron Disease 65 3.611
5
P HNT016 Huntington Disease 72 2.608
6
P ALZ034 Alzheimer Disease 88 2.334
7
DWN001 Down Syndrome 70 2.309
8
P FRN006 Frontotemporal Dementia 68 2.309
9
HYP066 Hyperglycemia 61 2.250
10
AGN016 Aging 56 2.233
11
ISC004 Ischemia 58 2.215
12
MLR004 Malaria 81 2.194
13
WLS001 Wilson Disease 71 2.194
14
P DBT009 Diabetes Mellitus 64 2.194
15
P MLN007 Male Infertility 55 2.194
16
c HYP595 Hypertension, Essential 84 2.171
17
c CHR684 Chronic Kidney Disease 70 2.171
18
SPT006 Septooptic Dysplasia 64 2.171
19
c PRC016 Pre-Eclampsia 63 2.171
20
P VSC007 Vascular Disease 63 2.171
21
LNG099 Lung Disease 60 2.171
22
P CTR002 Cataract 60 2.171
23
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 2.171
24
TNS005 Tonsillitis 57 2.171
25
P PNM006 Pneumoconiosis 56 2.171
26
BRN004 Brain Edema 56 2.171
27
SNL007 Senile Cataract 42 2.171
28
P NRB001 Neuroblastoma 72 2.019
29
P SPN046 Spinal Muscular Atrophy 62 1.963
30
P KRT007 Keratoconus 50 1.951
31
P PRK057 Parkinson Disease, Late-Onset 78 1.896
32
P MYP004 Myopathy 70 1.844
33
P DMN002 Dementia 66 1.844
34
P HYP097 Hyperekplexia 61 1.844
35
MYL020 Myelomeningocele 51 1.800
36
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.773
37
c DLT002 Dilated Cardiomyopathy 79 1.773
38
P SCH015 Schizophrenia 74 1.773
39
c HMC039 Hemochromatosis, Type 1 74 1.773
40
P CNR004 Cone-Rod Dystrophy 2 73 1.773
41
P ATS364 Autism 70 1.773
42
DFC004 Deficiency Anemia 70 1.773
43
CRB037 Cerebral Palsy 69 1.773
44
P CHR012 Chronic Granulomatous Disease 67 1.773
45
c ATS007 Autism Spectrum Disorder 67 1.773
46
P MCR115 Microvascular Complications of Diabetes 5 66 1.773
47
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.773
48
ACR006 Aceruloplasminemia 65 1.773
49
MNK001 Menkes Disease 64 1.773
50
P FRD001 Friedreich Ataxia 64 1.773
51
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 1.773
52
P GLY013 Glycogen Storage Disease 60 1.773
53
c SPN301 Spinocerebellar Ataxia 2 58 1.773
54
PST028 Post-Traumatic Stress Disorder 58 1.773
55
CNS004 Constipation 58 1.773
56
EXT034 Extrinsic Allergic Alveolitis 58 1.773
57
BRN056 Bronchopulmonary Dysplasia 57 1.773
58
P CRD246 Cardiovascular System Disease 57 1.773
59
VSC002 Vascular Dementia 57 1.773
60
RTN003 Retinal Ischemia 50 1.773
61
VRC001 Varicocele 49 1.773
62
P RNV001 Renovascular Hypertension 48 1.773
63
P MTH007 Methemoglobinemia 46 1.773
64
ELS001 Eales Disease 45 1.773
65
P MTC004 Mitochondrial Encephalomyopathy 44 1.773
66
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 42 1.773
67
P PYR039 Peyronie Disease 36 1.773
68
MLD002 Mild Pre-Eclampsia 36 1.773
69
PST030 Postcholecystectomy Syndrome 33 1.773
70
P RSP003 Respiratory Failure 74 1.503
71
NRM005 Neuromuscular Disease 64 1.380
72
P PRP019 Peripheral Nervous System Disease 58 1.361
73
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 1.361
74
P PRN023 Prion Disease 57 1.340
75
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 1.340
76
P CHR071 Charcot-Marie-Tooth Disease 65 1.317
77
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.289
78
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 1.289
79
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 1.289
80
ERY004 Erysipelas 49 1.289
81
MYC005 Myocardial Stunning 46 1.289
82
KR002 Kuru 45 1.289
83
c AMY090 Amyotrophic Lateral Sclerosis 8 43 1.289
84
P AMY106 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia 43 1.289
85
c PRG001 Progressive Muscular Atrophy 42 1.289
86
c AMY085 Amyotrophic Lateral Sclerosis 9 35 1.289
87
SPN022 Spinal Cord Neuroblastoma 16 1.289
88
P RTN008 Retinitis Pigmentosa 79 1.253
89
P TTR001 Tetralogy of Fallot 70 1.253
90
P MPL001 Maple Syrup Urine Disease 69 1.253
91
PCK003 Pick Disease of Brain 68 1.253
93
DMN031 Dementia, Lewy Body 65 1.253
94
P SHR029 Short Syndrome 63 1.253
95
TXC002 Toxic Encephalopathy 53 1.253
96
SCL003 Social Phobia 48 1.253
97
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 48 1.253
98
MNN020 Meningococcal Infection 46 1.253
99
c CRD226 Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive 46 1.253
100
HDN002 Head Injury 46 1.253
101
TTR005 Tetrahydrobiopterin Deficiency 45 1.253
102
c NRP044 Neuropathy, Hereditary Sensory and Autonomic, Type Viii 43 1.253
103
c ALZ045 Alzheimer Disease 9 43 1.253
104
P MLT008 Multinodular Goiter 42 1.253
105
ANX004 Anoxia 40 1.253
106
DRM021 Dermatopathia Pigmentosa Reticularis 39 1.253
107
HYP141 Hyperphenylalaninemia 39 1.253
108
ADN067 Adenoid Hypertrophy 39 1.253
109
c SPS100 Spastic Paraplegia 38, Autosomal Dominant 38 1.253
110
c AMY062 Amyotrophic Lateral Sclerosis 12 37 1.253
111
c CNG223 Congenital Methemoglobinemia 36 1.253
112
CHR028 Chronic Wasting Disease 35 1.253
113
PLT015 Platelet Aggregation, Spontaneous 34 1.253
114
c AMY059 Amyotrophic Lateral Sclerosis 19 34 1.253
115
PRG007 Progressive Bulbar Palsy 34 1.253
116
c CLR106 Ciliary Dyskinesia, Primary, 26 32 1.253
117
c AMY063 Amyotrophic Lateral Sclerosis 20 32 1.253
118
c AMY022 Amyotrophic Lateral Sclerosis Type 5 30 1.253
119
c AMY023 Amyotrophic Lateral Sclerosis Type 6 29 1.253
120
MNN024 Meningitis and Encephalitis 29 1.253
121
PRQ002 Paraquat Poisoning 26 1.253
122
SPN045 Spinal Cord Primitive Neuroectodermal Neoplasm 18 1.253
123
P MSC003 Muscular Atrophy 52 0.190
124
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.115
125
P NRP001 Neuropathy 56 0.107
126
CRB004 Cerebral Artery Occlusion 45 0.097
127
HRN029 Hearing Loss, Noise-Induced 37 0.097
128
P BRS047 Breast Cancer 97 0.087
129
c MCR113 Microvascular Complications of Diabetes 3 52 0.087
130
c MCR120 Microvascular Complications of Diabetes 7 47 0.087
131
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.087
132
c MCR130 Microvascular Complications of Diabetes 6 41 0.087
133
c MCR133 Microvascular Complications of Diabetes 4 41 0.087
134
MLT157 Multiple System Atrophy 1 70 0.075
135
P CRD119 Cardiac Arrest 67 0.075
136
INT002 Intermittent Claudication 61 0.075
137
SPN186 Spinal Cord Injury 60 0.075
138
EYD002 Eye Disease 58 0.075
139
P PLY019 Polyneuropathy 56 0.075
140
DYS073 Dysphagia 50 0.075
141
CHR178 Chromosomal Triplication 35 0.075
142
c KRT029 Keratoconus 1 33 0.075
143
P LNG032 Lung Cancer 98 0.062
145
P GST053 Gastric Cancer 83 0.062
146
GLB015 Glioblastoma Multiforme 75 0.062
147
P LVR013 Liver Disease 68 0.062
148
c RHB024 Rhabdomyosarcoma 2 67 0.062
149
P MSC005 Muscular Dystrophy 66 0.062
150
LSH001 Leishmaniasis 63 0.062
151
P HML002 Hemolytic Anemia 63 0.062
152
P END044 Endometriosis 63 0.062
153
c GLC092 Glaucoma, Primary Open Angle 62 0.062
154
c ANM038 Anemia, Autoimmune Hemolytic 62 0.062
155
ATM095 Autoimmune Disease 62 0.062
156
CTN007 Cutaneous Leishmaniasis 62 0.062
157
TXC005 Toxic Shock Syndrome 62 0.062
158
P THL005 Thalassemia 60 0.062
159
CHL014 Cholera 59 0.062
160
PRT058 Pure Autonomic Failure 59 0.062
161
P INF032 Infertility 57 0.062
162
SNS003 Sensory Peripheral Neuropathy 54 0.062
163
P RTN016 Retinal Degeneration 53 0.062
164
P OPN001 Open-Angle Glaucoma 49 0.062
165
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 47 0.062
166
SPS057 Spasticity 45 0.062
167
CYT002 Cytokine Deficiency 42 0.062
169
P KLZ004 Kala-Azar 1 41 0.062
170
WLL004 Wallerian Degeneration 39 0.062
171
PST092 Posttransplant Acute Limbic Encephalitis 29 0.062
172
PRX085 Preaxial Hallucal Polydactyly 28 0.062
173
P CLR023 Colorectal Cancer 99 0.043
174
STR067 Stroke, Ischemic 81 0.043
175
P BLD134 Bladder Cancer 79 0.043
176
INS024 Insulin-Like Growth Factor I 79 0.043
177
P LNG064 Lung Cancer Susceptibility 3 78 0.043
178
BRN028 Brain Cancer 74 0.043
179
c BTT014 Beta-Thalassemia 74 0.043
180
ULC004 Ulcerative Colitis 73 0.043
181
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.043
182
P GRF003 Graft-Versus-Host Disease 72 0.043
183
P PHC003 Pheochromocytoma 71 0.043
184
P EPL164 Epilepsy 71 0.043
185
P AMY004 Amyloidosis 70 0.043
186
CRT072 Creutzfeldt-Jakob Disease 70 0.043
187
P LKM002 Leukemia 68 0.043
188
FCT007 Factor Vii Deficiency 67 0.043
189
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.043
190
P NSP012 Nasopharyngeal Carcinoma 66 0.043
191
P ATR011 Atrial Fibrillation 66 0.043
192
c SML038 Small Cell Cancer of the Lung 65 0.043
193
P LPS002 Liposarcoma 65 0.043
194
P HRP006 Herpes Simplex 65 0.043
195
PRT036 Peritonitis 64 0.043
196
P GLM045 Glioma 63 0.043
197
P MVM001 Movement Disease 63 0.043
198
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.043
199
CLT003 Colitis 62 0.043
200
P MCH002 Machado-Joseph Disease 62 0.043
201
LPP008 Lipoprotein Quantitative Trait Locus 62 0.043
202
BLL006 Bullous Pemphigoid 62 0.043
203
ALL026 Allergic Hypersensitivity Disease 62 0.043
204
LVR012 Liver Cirrhosis 62 0.043
205
BLD131 Bladder Urothelial Carcinoma 62 0.043
206
FTT001 Fatty Liver Disease 61 0.043
207
P ENC004 Encephalitis 61 0.043
208
RTN017 Retinal Detachment 61 0.043
209
P TXP001 Toxoplasmosis 60 0.043
210
P SNS001 Sensorineural Hearing Loss 60 0.043
211
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.043
212
HYD002 Hydronephrosis 60 0.043
213
MTC097 Mitochondrial Complex Iv Deficiency 59 0.043
214
SPN027 Spinal Stenosis 59 0.043
215
INC002 Inclusion Body Myositis 58 0.043
216
P BCL017 B-Cell Lymphoma 58 0.043
217
LYM027 Lymphopenia 58 0.043
218
IRN002 Iron Metabolism Disease 57 0.043
219
c ACT075 Acute Myocardial Infarction 57 0.043
220
JPN002 Japanese Encephalitis 57 0.043
221
HYP266 Hypoxia 57 0.043
222
P BPL003 Bipolar Disorder 56 0.043
223
P MYS005 Myositis 56 0.043
224
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.043
225
NRG002 Neurogenic Bladder 55 0.043
226
P HYP076 Hyperthyroidism 55 0.043
227
GLC003 Glucose Intolerance 54 0.043
228
P INF037 Inflammatory Bowel Disease 54 0.043
229
P TRM003 Tremor 54 0.043
230
NNL006 Non-Alcoholic Steatohepatitis 54 0.043
231
P RTN018 Retinal Disease 53 0.043
232
CHR073 Choreatic Disease 52 0.043
233
DMY004 Demyelinating Disease 52 0.043
234
ART140 Arteries, Anomalies of 52 0.043
235
APR001 Apraxia 52 0.043
236
TRM010 Traumatic Brain Injury 51 0.043
237
P AST007 Astrocytoma 51 0.043
238
P OVR082 Overgrowth Syndrome 50 0.043
239
P MYS079 Miyoshi Muscular Dystrophy 50 0.043
240
DBT004 Diabetic Polyneuropathy 49 0.043
241
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.043
242
MCN001 Mucinous Adenocarcinoma 49 0.043
243
47X002 47,xyy 49 0.043
244
MNN009 Meningoencephalitis 49 0.043
245
BRN071 Brain Injury 49 0.043
246
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 49 0.043
247
BNR002 Bone Resorption Disease 48 0.043
248
P INN002 Inner Ear Disease 47 0.043
249
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.043
250
TTH006 Tooth Disease 46 0.043
251
ADR040 Adrenal Gland Pheochromocytoma 46 0.043
252
P MYC033 Myoclonus 46 0.043
253
GLL048 Glial Tumor 45 0.043
254
TRT001 Teratocarcinoma 45 0.043
255
APP009 Appendix Adenocarcinoma 44 0.043
256
FBR054 Fibroma 44 0.043
257
SDD008 Sudden Sensorineural Hearing Loss 43 0.043
258
LWC001 Low Compliance Bladder 43 0.043
259
DRG002 Drug-Induced Hepatitis 43 0.043
260
c PRG011 Progressive Myoclonus Epilepsy 42 0.043
261
c MJR024 Major Affective Disorder 9 41 0.043
262
PLY021 Polyradiculopathy 41 0.043
263
c PRG020 Paragangliomas 3 39 0.043
264
48X005 48,xyyy 39 0.043
265
SCR011 Scrapie 39 0.043
266
SPS019 Spastic Paraparesis 38 0.043
267
CDQ001 Cauda Equina Syndrome 38 0.043
268
PRN039 Paraneoplastic Syndromes 38 0.043
269
c MJR022 Major Affective Disorder 8 38 0.043
270
OCL015 Oculomotor Apraxia 37 0.043
271
P CRB059 Cerebellar Degeneration 37 0.043
272
P AXN001 Axonal Neuropathy 36 0.043
273
PSD088 Pseudobulbar Affect 36 0.043
274
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.043
275
P MYC026 Myoclonus Epilepsy 35 0.043
276
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.043
277
PLY150 Polykaryocytosis Inducer 31 0.043
278
SPN204 Spinal Muscular Atrophy, Late-Onset, Finkel Type 29 0.043
279
c AMY105 Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia 29 0.043
280
CRN009 Corneal Ectasia 28 0.043
281
ARG004 Argyria 27 0.043
282
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.043
Content
Loading form....