Search results for bace1

218 hits were found for bace1

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 87 31.887
2
P AMY004 Amyloidosis 69 16.465
3
P NRB001 Neuroblastoma 66 16.454
4
DWN001 Down Syndrome 70 15.464
5
P DMN002 Dementia 65 14.588
6
P MYS005 Myositis 55 14.579
7
CRT072 Creutzfeldt-Jakob Disease 67 13.657
9
P SCH015 Schizophrenia 74 12.092
10
VSC002 Vascular Dementia 59 12.071
11
MLD018 Mild Cognitive Impairment 48 11.280
12
STR067 Stroke, Ischemic 79 10.320
13
P PRK057 Parkinson Disease, Late-Onset 79 10.220
14
c AMY091 Amyotrophic Lateral Sclerosis 1 87 8.100
15
c ALZ056 Alzheimer Disease 3 56 7.267
16
DMN031 Dementia, Lewy Body 65 7.129
17
c ALZ054 Alzheimer Disease 4 44 7.129
18
c DVL037 Developmental and Epileptic Encephalopathy 5 45 7.129
19
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 53 7.129
20
PCK003 Pick Disease of Brain 70 7.129
21
P SPR120 Supranuclear Palsy, Progressive, 1 68 7.129
22
P CHR084 Chromosomal Disease 35 7.129
23
CHR569 Chromosomal Duplication Syndrome 23 7.129
24
NCT001 Necatoriasis 21 7.129
25
ACT016 Actinobacillosis 31 7.129
26
P PRP019 Peripheral Nervous System Disease 57 7.129
27
DSS008 Disease of Mental Health 74 7.129
28
TXC002 Toxic Encephalopathy 51 7.129
29
P NRV007 Nervous System Disease 65 7.129
30
HYP266 Hypoxia 56 2.360
31
INC002 Inclusion Body Myositis 56 2.231
32
GLC003 Glucose Intolerance 53 2.008
33
P PHC003 Pheochromocytoma 70 1.772
34
ADR040 Adrenal Gland Pheochromocytoma 45 1.772
36
CRT015 Carotid Artery Occlusion 45 1.556
37
P OVR042 Ovarian Cancer 88 1.522
38
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.512
39
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.496
40
ATH013 Atherosclerosis Susceptibility 63 1.480
41
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.480
42
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.464
43
P PRN023 Prion Disease 60 1.464
44
GLB002 Glioblastoma 67 1.411
45
TRM010 Traumatic Brain Injury 50 1.405
46
FTT001 Fatty Liver Disease 61 1.352
47
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.336
48
CRB039 Cerebrovascular Disease 65 1.309
49
HLX001 Helix Syndrome 47 1.279
50
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.234
51
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 1.234
52
c HYP836 Hypercholesterolemia, Familial, 1 73 1.201
53
P BCL017 B-Cell Lymphoma 57 1.201
54
P ENC018 Encephalopathy 62 1.201
55
BRN071 Brain Injury 50 1.171
56
SNL009 Senile Plaque Formation 28 1.167
57
P GLM040 Glioma Susceptibility 1 70 1.130
58
P HPT023 Hepatocellular Carcinoma 95 1.130
59
MLG169 Malignant Astrocytoma 57 1.130
60
P TMP001 Temporal Lobe Epilepsy 49 1.110
61
P VSC007 Vascular Disease 62 1.090
62
P SZR006 Seizure Disorder 69 1.069
63
c MJR022 Major Affective Disorder 8 37 1.047
64
c MJR024 Major Affective Disorder 9 40 1.047
65
RTN020 Retinal Vascular Disease 45 1.047
66
P PLY020 Polyradiculoneuropathy 47 1.047
67
P BPL003 Bipolar Disorder 56 1.047
68
P PNC044 Pancreatitis 61 1.047
69
c ACT027 Acute Pancreatitis 60 1.047
70
ATY012 Atypical Mycobacteriosis, Familial 34 1.047
71
CRB090 Cerebral Hypoxia 42 1.047
72
c ATS007 Autism Spectrum Disorder 71 1.023
73
P MLT020 Multiple Sclerosis 79 1.023
74
ATM095 Autoimmune Disease 61 1.023
75
c SPN294 Spinocerebellar Ataxia 1 53 1.023
76
TRN015 Transient Cerebral Ischemia 62 1.023
77
P MJR001 Major Depressive Disorder 68 0.998
78
IMP005 Impotence 52 0.998
79
MNT002 Mental Depression 56 0.998
80
P HRP006 Herpes Simplex 65 0.998
81
DPR016 Depression 64 0.998
82
c SPN296 Spinocerebellar Ataxia 17 48 0.971
83
P LTR001 Lateral Sclerosis 57 0.971
84
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.971
85
P MYP004 Myopathy 67 0.971
86
SBC016 Subacute Delirium 42 0.971
87
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.941
88
MSC007 Muscle Hypertrophy 64 0.941
89
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.941
90
ASY002 Asymptomatic Neurosyphilis 41 0.941
91
AMN003 Amnestic Disorder 53 0.941
92
GLM045 Glioma 62 0.941
93
ALL014 Allergic Encephalomyelitis 34 0.941
94
NRS003 Neurosyphilis 45 0.941
95
GLL048 Glial Tumor 51 0.941
96
c MGR028 Migraine with or Without Aura 1 63 0.909
97
c PCH010 Pachyonychia Congenita 3 43 0.909
98
RCK004 Rickets 64 0.909
99
RBS001 Rabies 57 0.872
100
P HYP069 Hyperparathyroidism 62 0.872
101
c SCN007 Secondary Hyperparathyroidism 50 0.872
102
P BRS047 Breast Cancer 97 0.779
103
P MJR007 Major Affective Disorder 1 42 0.771
104
c TYP009 Type 2 Diabetes Mellitus 91 0.660
105
CRB004 Cerebral Artery Occlusion 45 0.660
106
c SML038 Small Cell Cancer of the Lung 68 0.633
107
P LNG032 Lung Cancer 98 0.633
108
CRB033 Cerebral Degeneration 36 0.633
109
HYP066 Hyperglycemia 60 0.584
110
P DBT009 Diabetes Mellitus 67 0.551
111
P PNC035 Pancreatic Cancer 87 0.551
112
P LKM062 Leukemia, Acute Lymphoblastic 69 0.551
113
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.471
114
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.457
115
AGN016 Aging 53 0.457
116
FRN006 Frontotemporal Dementia 68 0.436
117
P ANP001 Anaplastic Large Cell Lymphoma 59 0.390
118
HVY002 Heavy Metal Poisoning 22 0.390
119
ANX010 Anxiety 70 0.364
120
SBJ001 Subjective Cognitive Decline 29 0.364
121
LPD008 Lipid Metabolism Disorder 61 0.364
122
ISC004 Ischemia 61 0.364
123
CHL078 Childhood-Onset Schizophrenia 29 0.364
124
c ERL020 Early-Onset Schizophrenia 43 0.364
125
c SCH079 Schizophrenia 1 44 0.337
126
P DRM053 Dermatitis, Atopic 65 0.337
127
P GST053 Gastric Cancer 82 0.337
128
P FRG001 Fragile X Syndrome 70 0.337
129
P HNT016 Huntington Disease 73 0.337
130
HMS001 Hemosiderosis 48 0.337
131
GRN055 Granular Corneal Dystrophy 36 0.337
132
P CRN025 Corneal Dystrophy 49 0.337
133
SKN016 Skin Disease 63 0.337
134
CHR178 Chromosomal Triplication 33 0.337
135
P RRH023 Rare Hereditary Hemochromatosis 52 0.337
136
SPN186 Spinal Cord Injury 60 0.337
137
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.308
138
c SPN291 Spinocerebellar Ataxia 7 50 0.308
139
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.308
140
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.308
141
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.308
142
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.308
143
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.308
144
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.308
145
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.308
146
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.308
147
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.308
148
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.308
149
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.308
150
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.308
151
CHL123 Chlamydia 58 0.308
152
P BRB001 Beriberi 44 0.308
153
CHL147 Chlamydia Pneumonia 47 0.308
154
P EPL164 Epilepsy 70 0.308
155
CRB008 Cerebral Atherosclerosis 45 0.308
157
P TRM003 Tremor 50 0.308
158
ALV005 Alveolar Soft Part Sarcoma 61 0.275
159
c PRD040 Periodontitis, Chronic 52 0.275
160
HMC014 Homocysteinemia 52 0.275
161
CHL014 Cholera 62 0.275
162
P PRD008 Periodontitis 63 0.275
164
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.239
165
P OST002 Osteoporosis 76 0.239
166
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.239
167
P EXN002 Exanthem 58 0.239
168
c TYP008 Type 1 Diabetes Mellitus 77 0.239
169
P HYP750 Hypertriglyceridemia, Familial 61 0.239
170
DBT081 Diabetic Encephalopathy 36 0.239
171
HYP060 Hyperinsulinism 53 0.239
172
SVR004 Severe Combined Immunodeficiency 70 0.239
173
P KDN018 Kidney Disease 71 0.239
174
P GST044 Gastritis 55 0.239
175
P ATR005 Atrophic Gastritis 50 0.239
176
c CHR684 Chronic Kidney Disease 73 0.239
177
P CHR345 Chronic Pain 50 0.239
178
c NMN014 Niemann-Pick Disease, Type C2 49 0.195
180
P ATS364 Autism 72 0.195
181
CRD223 Cardiac Arrhythmia 63 0.195
182
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.195
183
P DVL113 Developmental and Epileptic Encephalopathy 46 0.195
184
SCR011 Scrapie 39 0.195
185
P RTN018 Retinal Disease 53 0.195
186
HPP002 Huppke-Brendel Syndrome 7 0.195
187
P MYC008 Myocarditis 59 0.195
188
P CRB088 Cerebral Atrophy 32 0.195
189
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.138
190
APH002 Aphasia 55 0.138
191
P PLV020 Pelvic Organ Prolapse 57 0.138
192
c GLC092 Glaucoma, Primary Open Angle 60 0.138
193
P HRS035 Hirschsprung Disease 1 66 0.138
194
INS024 Insulin-Like Growth Factor I 77 0.138
195
c THY107 Thymoma, Familial 42 0.138
196
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.138
197
P MYS003 Myasthenia Gravis 67 0.138
198
c NMN015 Niemann-Pick Disease, Type C1 68 0.138
199
P WSK001 Wiskott-Aldrich Syndrome 72 0.138
200
TBL029 Tubulin, Beta 28 0.138
201
P ASP006 Aspergillosis 71 0.138
202
MLT157 Multiple System Atrophy 1 69 0.138
203
IGR001 Ige Responsiveness, Atopic 58 0.138
204
P RNV001 Renovascular Hypertension 48 0.138
205
P THY023 Thymoma 64 0.138
206
IRN002 Iron Metabolism Disease 56 0.138
207
SVR001 Severe Acute Respiratory Syndrome 68 0.138
208
P OPN001 Open-Angle Glaucoma 55 0.138
209
P HYD006 Hydrocephalus 62 0.138
210
KRT002 Keratomalacia 54 0.138
211
c PRC016 Pre-Eclampsia 64 0.138
212
P SLP005 Sleep Disorder 61 0.138
213
ALL006 Allergic Asthma 55 0.138
214
P RTN016 Retinal Degeneration 52 0.138
215
48X005 48,xyyy 39 0.138
216
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.138
217
HYP056 Hypoglycemia 65 0.138
218
SPS057 Spasticity 43 0.138
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