Search results for (neurodegenerative OR senile) AND Alzheimer

260 hits were found for (neurodegenerative OR senile) AND Alzheimer

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 87 11.713
2
DMN031 Dementia, Lewy Body 66 2.022
3
DMN002 Dementia 68 1.032
4
AGN016 Aging 64 0.667
5
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.619
6
P ENC018 Encephalopathy 62 0.575
7
NRN002 Neuronitis 41 0.561
8
c CNT035 Central Nervous System Disease 63 0.475
9
CRB009 Cerebritis 41 0.446
10
P AMY004 Amyloidosis 68 0.433
11
VSC002 Vascular Dementia 58 0.354
12
P FRN006 Frontotemporal Dementia 67 0.276
13
DPR016 Depression 72 0.275
14
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.273
15
c CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 63 0.251
16
DWN001 Down Syndrome 69 0.226
17
c ALZ049 Alzheimer Disease 2 59 0.226
18
P CTR002 Cataract 60 0.212
19
PCK003 Pick Disease of Brain 65 0.210
20
P PRK057 Parkinson Disease, Late-Onset 76 0.193
21
ANX010 Anxiety 72 0.183
22
APH002 Aphasia 58 0.178
23
P SCH015 Schizophrenia 69 0.172
24
SPS057 Spasticity 41 0.168
25
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.164
26
c ALZ062 Alzheimer Disease 19 28 0.158
27
CRB039 Cerebrovascular Disease 67 0.158
28
END072 Endotheliitis 45 0.158
29
P HYD006 Hydrocephalus 69 0.155
30
SMN008 Semantic Dementia 54 0.154
31
MVM001 Movement Disease 60 0.152
32
P NRV007 Nervous System Disease 73 0.151
33
APR001 Apraxia 53 0.150
34
PST086 Posterior Cortical Atrophy 41 0.143
35
P DBT009 Diabetes Mellitus 64 0.142
36
SPS003 Spastic Diplegia 54 0.142
37
RTN023 Retinitis 50 0.139
38
MNT002 Mental Depression 57 0.139
39
CLS047 Classic Progressive Supranuclear Palsy Syndrome 28 0.137
40
ANS006 Anosognosia 28 0.136
41
CRT072 Creutzfeldt-Jakob Disease 65 0.132
42
c MCL042 Macular Degeneration, Age-Related, 1 84 0.126
43
P EPL164 Epilepsy 69 0.125
44
P CRB088 Cerebral Atrophy 39 0.124
45
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.122
46
BSL008 Basal Ganglia Disease 46 0.122
47
c ALZ054 Alzheimer Disease 4 41 0.117
48
c ESS001 Essential Tremor 57 0.111
49
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.108
50
c ALZ056 Alzheimer Disease 3 47 0.108
51
P HRT032 Heart Disease 74 0.107
52
PSY004 Psychotic Disorder 71 0.107
53
CRT033 Corticobasal Degeneration 52 0.106
54
BRN071 Brain Injury 53 0.104
55
P LTR001 Lateral Sclerosis 58 0.104
56
c ALZ045 Alzheimer Disease 9 21 0.104
57
P OST002 Osteoporosis 76 0.103
58
P OPN001 Open-Angle Glaucoma 51 0.102
59
HYD061 Hydrocephalus, Normal-Pressure 47 0.102
60
P MLT020 Multiple Sclerosis 78 0.099
61
P THY032 Thyroiditis 55 0.097
62
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.097
63
SLP005 Sleep Disorder 59 0.097
64
SNL009 Senile Plaque Formation 27 0.095
65
SPC010 Speech and Communication Disorders 52 0.093
66
INC002 Inclusion Body Myositis 63 0.091
67
BNS003 Binswanger's Disease 45 0.091
68
PRN023 Prion Disease 50 0.090
69
TYP041 Type I 56 0.089
70
P LYM118 Lymphoma 70 0.089
71
SPS019 Spastic Paraparesis 35 0.089
72
c GRN014 Grn-Related Frontotemporal Dementia 37 0.088
73
P AGN002 Agnosia 61 0.087
74
PRM153 Primary Progressive Apraxia of Speech 21 0.086
75
KR002 Kuru 38 0.083
76
ISC004 Ischemia 65 0.082
77
P ENC004 Encephalitis 65 0.082
78
ALZ029 Alzheimer Disease Mitochondrial 23 0.082
79
P NRB001 Neuroblastoma 72 0.082
80
P ANR048 Aniridia 1 65 0.081
81
BLD137 Blood Group--Ahonen 17 0.081
82
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.081
83
TRM010 Traumatic Brain Injury 55 0.080
84
HDN002 Head Injury 47 0.080
85
P MYP006 Myopia 56 0.079
86
HYP266 Hypoxia 61 0.079
87
ART140 Arteries, Anomalies of 65 0.079
88
P TRM003 Tremor 54 0.076
89
c GLC092 Glaucoma, Primary Open Angle 57 0.076
90
VSC007 Vascular Disease 68 0.076
91
MLT157 Multiple System Atrophy 1 73 0.075
92
CPG001 Capgras Syndrome 24 0.075
93
MDD011 Mood Disorder 63 0.072
94
c ALZ032 Alzheimer Disease 18 17 0.072
95
P LKM002 Leukemia 72 0.071
96
SPC005 Speech Disorder 47 0.071
97
P ART021 Arteriosclerosis 60 0.070
98
RMS001 Rem Sleep Behavior Disorder 42 0.070
99
c CHR579 Chiari Malformation Type Ii 45 0.068
100
c ALZ015 Alzheimer Disease 6 23 0.068
101
P SLP006 Sleep Apnea 66 0.068
102
BLL006 Bullous Pemphigoid 63 0.067
103
CHR008 Choroiditis 46 0.064
104
P NRP001 Neuropathy 63 0.062
105
P MYS005 Myositis 63 0.060
106
BHV002 Behavioral Variant of Frontotemporal Dementia 40 0.060
107
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 59 0.060
108
P HNT016 Huntington Disease 70 0.059
109
SYN058 Synucleinopathy 41 0.059
110
STR067 Stroke, Ischemic 82 0.059
111
DMN026 Dementia Pugilistica 24 0.058
112
ALR002 Al-Raqad Syndrome 31 0.057
113
BRN080 Brain Ischemia 44 0.056
114
c ART101 Aortic Valve Disease 2 73 0.055
115
P CRN018 Coronary Artery Anomaly 68 0.055
116
GTP001 Gait Apraxia 37 0.055
117
ATM095 Autoimmune Disease 64 0.055
118
MYC033 Myoclonus 41 0.054
119
AST005 Asthma 82 0.054
120
PRG033 Progressive Non-Fluent Aphasia 48 0.054
121
INS024 Insulin-Like Growth Factor I 82 0.053
122
c MTR002 Mitral Valve Insufficiency 46 0.053
123
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.053
124
APN008 Apnea, Obstructive Sleep 67 0.052
125
P LKD001 Leukodystrophy 57 0.052
126
GT001 Gout 57 0.051
127
MTR014 Motor Neuron Disease 61 0.050
128
ATN005 Autonomic Dysfunction 50 0.049
129
P OLV001 Olivopontocerebellar Atrophy 50 0.048
130
P PNC044 Pancreatitis 64 0.048
131
SCR011 Scrapie 40 0.048
132
P MYC007 Myocardial Infarction 79 0.048
133
GLC003 Glucose Intolerance 56 0.048
134
ALZ052 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology 10 0.048
135
DYS073 Dysphagia 46 0.046
136
PRS047 Prostatitis 60 0.045
137
CRB008 Cerebral Atherosclerosis 41 0.045
138
CNG034 Congestive Heart Failure 72 0.044
139
NRS003 Neurosyphilis 45 0.044
140
P FML043 Familial Idiopathic Basal Ganglia Calcification 41 0.044
141
P NRC002 Narcolepsy 63 0.042
142
RTN018 Retinal Disease 56 0.042
143
P EXN002 Exanthem 61 0.042
144
c CRN300 Coronary Heart Disease 1 64 0.041
145
RST001 Restless Legs Syndrome 52 0.041
146
P DYS021 Dysautonomia 43 0.041
147
DMY004 Demyelinating Disease 57 0.040
148
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.040
149
P CMM008 Communicating Hydrocephalus 35 0.040
150
ALP046 Alport Syndrome, X-Linked 75 0.040
151
P RTN016 Retinal Degeneration 54 0.040
152
LNS003 Lens Disease 39 0.039
153
P PRD008 Periodontitis 66 0.039
154
CYT008 Cytomegalovirus Infection 56 0.039
155
P GLM045 Glioma 54 0.039
156
CRB033 Cerebral Degeneration 42 0.039
157
ACR006 Aceruloplasminemia 73 0.038
158
NRM005 Neuromuscular Disease 60 0.038
159
c NMN015 Niemann-Pick Disease, Type C1 68 0.038
160
P NMN002 Niemann-Pick Disease 60 0.038
161
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 52 0.038
162
P TYS001 Tay-Sachs Disease 71 0.036
163
P SPN301 Spinocerebellar Ataxia 2 56 0.036
164
SPN041 Spinal Cord Disease 51 0.036
165
HYP066 Hyperglycemia 63 0.036
166
LMB024 Limbic Encephalitis 41 0.036
167
ADN018 Adenoma 63 0.035
168
CRB087 Cerebral Arteriosclerosis 20 0.035
169
P PRS040 Prostate Cancer 90 0.035
170
WLS001 Wilson Disease 71 0.035
171
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 66 0.035
172
P INF032 Infertility 59 0.035
173
LPD008 Lipid Metabolism Disorder 58 0.035
174
ACT049 Acute Disseminated Encephalomyelitis 50 0.035
175
PNN005 Panencephalitis, Subacute Sclerosing 43 0.035
176
ADS004 Aids Dementia Complex 41 0.035
177
FXF002 Fox-Fordyce Disease 40 0.035
178
PST027 Postencephalitic Parkinson Disease 39 0.035
179
P STR001 Striatonigral Degeneration 33 0.035
180
P ATX030 Ataxia-Telangiectasia 79 0.033
181
BRN028 Brain Cancer 72 0.033
182
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.033
183
FTL002 Fatal Familial Insomnia 49 0.033
184
c PRG011 Progressive Myoclonus Epilepsy 38 0.033
185
P MYC026 Myoclonus Epilepsy 36 0.033
186
PRP030 Purpura 61 0.032
187
P PLY019 Polyneuropathy 57 0.032
188
P BLD051 Blood Coagulation Disease 50 0.032
189
P FRD012 Friedreich Ataxia 1 64 0.032
190
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.032
191
P LVR013 Liver Disease 75 0.031
192
ISC006 Ischemic Heart Disease 72 0.031
193
P LYM026 Lymphoblastic Leukemia 64 0.031
194
HMT002 Hematologic Cancer 63 0.031
195
HMR039 Hemorrhage, Intracerebral 57 0.031
196
P CRB059 Cerebellar Degeneration 39 0.031
197
c BLD140 Blood Group, I System 23 0.031
198
c CRD182 Ceroid Lipofuscinosis, Neuronal, 10 43 0.030
199
NRL016 Neural Tube Defects 78 0.030
200
P FRG001 Fragile X Syndrome 69 0.030
201
P DYS154 Dystonia 64 0.030
202
PRP019 Peripheral Nervous System Disease 60 0.030
203
OPT006 Optic Nerve Disease 57 0.030
204
TCD001 Tic Disorder 54 0.030
205
P AST007 Astrocytoma 51 0.030
206
EXC002 Exocrine Pancreatic Insufficiency 43 0.030
207
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 40 0.030
208
NRX001 Neuroaxonal Dystrophy 40 0.030
209
MHR001 Mohr-Tranebjaerg Syndrome 39 0.030
210
P PRS013 Prosopagnosia 34 0.030
211
HYP080 Hypogonadism 51 0.029
212
BNM029 Bone Mineral Density Quantitative Trait Locus 15 38 0.029
213
ADR007 Adrenoleukodystrophy 71 0.027
214
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 59 0.027
215
CRN031 Cranial Nerve Disease 45 0.027
216
ATM052 Autoimmune Disease 1 34 0.027
217
OST012 Osteoarthritis 82 0.025
218
P HYP607 Hypercholesterolemia, Familial 79 0.025
219
c LKM062 Leukemia, Acute Lymphoblastic 69 0.025
220
BDY004 Body Mass Index Quantitative Trait Locus 11 68 0.025
221
P ANT006 Antiphospholipid Syndrome 59 0.025
222
LYM019 Lymphosarcoma 55 0.025
223
PRP016 Paraplegia 53 0.025
224
RTN209 Retinoschisis 1, X-Linked, Juvenile 53 0.025
225
RNP003 Renpenning Syndrome 1 52 0.025
226
c ART119 Arthrogryposis, Distal, Type 5 49 0.025
227
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.025
228
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 42 0.025
229
BDY019 Body Mass Index Quantitative Trait Locus 18 27 0.025
230
BDY005 Body Mass Index Quantitative Trait Locus 9 27 0.025
231
BDY015 Body Mass Index Quantitative Trait Locus 12 25 0.025
232
BDY017 Body Mass Index Quantitative Trait Locus 14 25 0.025
233
BDY010 Body Mass Index Quantitative Trait Locus 4 25 0.025
234
BDY020 Body Mass Index Quantitative Trait Locus 19 25 0.025
235
BDY011 Body Mass Index Quantitative Trait Locus 10 24 0.025
236
BDY006 Body Mass Index Quantitative Trait Locus 8 23 0.025
237
BDY012 Body Mass Index Quantitative Trait Locus 7 23 0.025
238
SBC025 Subcortical Arteriosclerotic Encephalopathy 18 0.025
239
URT002 Urethral Intrinsic Sphincter Deficiency 17 0.025
240
CNN003 Conn's Syndrome 71 0.024
241
SPN186 Spinal Cord Injury 68 0.024
242
LNG099 Lung Disease 67 0.024
243
PRD007 Periodontal Disease 64 0.024
244
MNK001 Menkes Disease 63 0.024
245
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 63 0.024
246
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.024
247
OVR063 Overnutrition 53 0.024
248
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 52 0.024
249
HMS001 Hemosiderosis 51 0.024
250
ATN002 Autonomic Nervous System Disease 51 0.024
251
RTN003 Retinal Ischemia 50 0.024
252
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.024
253
HRT007 Heart Cancer 43 0.024
254
OCL069 Ocular Motor Apraxia 42 0.024
255
OCL011 Ocular Motility Disease 41 0.024
256
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 39 0.024
257
CHR073 Choreatic Disease 37 0.024
258
PRR004 Preretinal Fibrosis 35 0.024
259
c PRK085 Parkinson Disease 1, Autosomal Dominant 31 0.024
260
MTR031 Motor Neuro-Ophthalmic Disorders 20 0.024
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