Search results for (neurodegenerative OR senile) AND Alzheimer

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

# Family MCID Name MIFTS Score
1
ALZ034 Alzheimer Disease 86 11.291
2
DMN031 Dementia, Lewy Body 67 1.998
3
DMN002 Dementia 68 1.007
4
AGN016 Aging 62 0.452
5
VSC002 Vascular Dementia 55 0.419
6
AMY004 Amyloidosis 68 0.408
7
c CNT035 Central Nervous System Disease 62 0.388
8
FRN006 Frontotemporal Dementia 67 0.338
9
FRN030 Frontotemporal Dementia with Parkinsonism-17 32 0.297
10
DPR016 Depression 73 0.239
11
DWN001 Down Syndrome 72 0.239
13
c ALZ049 Alzheimer Disease 2 60 0.205
14
CTR002 Cataract 58 0.203
15
BNS003 Binswanger\'s Disease 45 0.184
16
PCK003 Pick Disease of Brain 64 0.183
17
SPR120 Supranuclear Palsy, Progressive, 1 71 0.176
18
APH002 Aphasia 60 0.176
19
ENC018 Encephalopathy 62 0.170
20
SCH015 Schizophrenia 70 0.165
21
HYD006 Hydrocephalus 66 0.158
22
CRB039 Cerebrovascular Disease 67 0.158
23
TRC086 Trichohepatoenteric Syndrome 1 51 0.152
24
APR001 Apraxia 54 0.151
25
DBT009 Diabetes Mellitus 67 0.146
26
ANX010 Anxiety 72 0.145
27
c ALZ062 Alzheimer Disease 19 32 0.141
28
EPL164 Epilepsy 73 0.141
29
CRT072 Creutzfeldt-Jakob Disease 66 0.139
30
VSC007 Vascular Disease 68 0.137
31
NRV007 Nervous System Disease 69 0.137
32
TRM003 Tremor 55 0.135
33
SMN008 Semantic Dementia 51 0.134
35
PST086 Posterior Cortical Atrophy 41 0.124
36
SPS003 Spastic Diplegia 54 0.123
37
ANS006 Anosognosia 30 0.119
38
c ESS001 Essential Tremor 58 0.118
39
BSL008 Basal Ganglia Disease 43 0.117
40
PRN023 Prion Disease 54 0.115
41
MNT002 Mental Depression 62 0.114
42
MLT157 Multiple System Atrophy 1 74 0.112
43
c ALZ054 Alzheimer Disease 4 45 0.112
44
LTR001 Lateral Sclerosis 60 0.109
45
CRB088 Cerebral Atrophy 38 0.108
46
MLT020 Multiple Sclerosis 75 0.108
47
c AMY091 Amyotrophic Lateral Sclerosis 1 91 0.108
48
BRN071 Brain Injury 54 0.106
49
HRT032 Heart Disease 73 0.106
50
HYD061 Hydrocephalus, Normal-Pressure 50 0.102
51
CRT033 Corticobasal Degeneration 54 0.100
52
PRK057 Parkinson Disease, Late-Onset 76 0.098
53
c ALZ045 Alzheimer Disease 9 24 0.098
54
OPN001 Open-Angle Glaucoma 53 0.096
55
OST002 Osteoporosis 74 0.095
56
c ALZ056 Alzheimer Disease 3 48 0.095
57
PSY004 Psychotic Disorder 72 0.093
58
HNT016 Huntington Disease 73 0.092
60
SLP005 Sleep Disorder 57 0.089
61
LYM118 Lymphoma 70 0.087
62
SNL009 Senile Plaque Formation 27 0.087
63
HDN002 Head Injury 48 0.086
64
TRM010 Traumatic Brain Injury 56 0.086
65
BLL006 Bullous Pemphigoid 65 0.086
66
INC002 Inclusion Body Myositis 66 0.084
67
PST027 Postencephalitic Parkinson Disease 44 0.082
68
KR002 Kuru 39 0.080
70
CHR073 Choreatic Disease 47 0.079
71
AGN002 Agnosia 56 0.079
72
PRM153 Primary Progressive Apraxia of Speech 13 0.078
73
ISC004 Ischemia 66 0.077
74
c GLC092 Glaucoma, Primary Open Angle 58 0.077
75
ALZ029 Alzheimer Disease Mitochondrial 29 0.077
76
HYP266 Hypoxia 62 0.077
77
ATX030 Ataxia-Telangiectasia 84 0.076
78
ENC004 Encephalitis 66 0.075
79
SPS019 Spastic Paraparesis 35 0.075
80
ATX010 Ataxia Neuropathy Spectrum 32 0.074
81
ANR007 Anorexia Nervosa 68 0.073
82
ACN002 Acanthosis Nigricans 66 0.073
83
ANR048 Aniridia 1 65 0.073
84
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 46 0.073
85
ACT232 Acute Necrotizing Encephalopathy 33 0.073
86
BLD137 Blood Group--Ahonen 24 0.073
87
DMN026 Dementia Pugilistica 28 0.072
88
PTL001 Patulous Eustachian Tube 32 0.072
89
ERL001 Early Myoclonic Encephalopathy 53 0.071
90
RMS001 Rem Sleep Behavior Disorder 43 0.071
91
ART153 Arthrochalasia Ehlers-Danlos Syndrome 24 0.070
92
SLP006 Sleep Apnea 70 0.069
93
NRB001 Neuroblastoma 73 0.069
94
HRP006 Herpes Simplex 70 0.069
95
CRB085 Cerebral Hemorrhage 45 0.068
96
CPG001 Capgras Syndrome 25 0.067
97
LKM002 Leukemia 72 0.066
98
KRT002 Keratomalacia 56 0.065
99
TCD001 Tic Disorder 55 0.065
100
THR013 Thoracic Outlet Syndrome 55 0.065
101
ART021 Arteriosclerosis 57 0.064
102
STR067 Stroke, Ischemic 85 0.064
103
PNN005 Panencephalitis, Subacute Sclerosing 44 0.064
104
MJR001 Major Depressive Disorder 66 0.063
105
SPC005 Speech Disorder 44 0.063
106
MDD011 Mood Disorder 62 0.062
107
c ALZ015 Alzheimer Disease 6 19 0.062
108
c ALZ032 Alzheimer Disease 18 16 0.062
109
ANG001 Angelman Syndrome 67 0.062
110
PLY019 Polyneuropathy 58 0.062
111
c ALZ063 Alzheimer\'s Disease 1 29 0.061
112
c SPN225 Spondyloarthropathy 1 75 0.060
113
c CHR579 Chiari Malformation Type Ii 42 0.059
114
INS024 Insulin-Like Growth Factor I 76 0.057
115
BRN080 Brain Ischemia 41 0.057
116
INT002 Intermittent Claudication 63 0.055
117
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 55 0.055
118
ATM095 Autoimmune Disease 65 0.055
119
NRP001 Neuropathy 62 0.054
120
ATS308 Autosomal Dominant Cerebellar Ataxia 57 0.054
121
NRT004 Neuritis 55 0.053
122
AND002 Androgen Insensitivity Syndrome 65 0.053
123
AXN002 Axenfeld-Rieger Syndrome 56 0.053
124
ALR002 Al-Raqad Syndrome 41 0.053
125
SYN058 Synucleinopathy 44 0.053
126
MYS005 Myositis 64 0.052
127
BHV002 Behavioral Variant of Frontotemporal Dementia 42 0.052
128
MYC033 Myoclonus 43 0.052
129
RHM011 Rheumatoid Arthritis 82 0.051
130
MTR014 Motor Neuron Disease 59 0.050
131
LKD001 Leukodystrophy 57 0.050
132
GLC003 Glucose Intolerance 58 0.050
133
AST005 Asthma 82 0.049
134
VRL011 Viral Infectious Disease 72 0.049
135
PNM007 Pneumonia 71 0.048
136
c MTR002 Mitral Valve Insufficiency 48 0.048
137
TLN003 Telangiectasis 54 0.048
138
RTN018 Retinal Disease 56 0.048
139
DYS073 Dysphagia 51 0.047
140
c CNG216 Congenital Hydrocephalus 47 0.047
141
BPL003 Bipolar Disorder 60 0.047
142
GTP001 Gait Apraxia 34 0.047
143
ACR001 Aicardi-Goutieres Syndrome 61 0.047
144
c ACR116 Aicardi-Goutieres Syndrome 1 44 0.047
145
ALZ052 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology 10 0.047
146
PRG033 Progressive Non-Fluent Aphasia 49 0.047
147
MYC007 Myocardial Infarction 77 0.045
148
CRB033 Cerebral Degeneration 43 0.045
149
ARG004 Argyria 28 0.044
150
LPD008 Lipid Metabolism Disorder 64 0.044
151
ACT049 Acute Disseminated Encephalomyelitis 56 0.044
152
HMC014 Homocysteinemia 54 0.044
153
ICH020 Ichthyosis Prematurity Syndrome 45 0.044
154
BLD153 Blood Group--Swann System 25 0.043
155
APN008 Apnea, Obstructive Sleep 68 0.043
156
OLV001 Olivopontocerebellar Atrophy 53 0.043
157
ATS364 Autism 69 0.042
158
GT001 Gout 60 0.042
159
TMP001 Temporal Lobe Epilepsy 57 0.042
160
SCR011 Scrapie 37 0.042
161
CGN007 Cognitive Function 1, Social 35 0.042
162
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.041
163
c CRN300 Coronary Heart Disease 1 59 0.040
164
ALP046 Alport Syndrome, X-Linked 74 0.040
165
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.040
166
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.040
167
HYP066 Hyperglycemia 64 0.040
168
ART001 Arterial Tortuosity Syndrome 60 0.040
169
KHL003 Kohlschutter-Tonz Syndrome 52 0.040
170
HPT082 Hepatic Adenomas, Familial 51 0.040
171
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.040
172
ADP007 Adie Pupil 43 0.040
173
FML043 Familial Idiopathic Basal Ganglia Calcification 43 0.040
174
SPS057 Spasticity 42 0.040
175
HNM002 Hinman Syndrome 32 0.040
176
NRM005 Neuromuscular Disease 58 0.040
177
DMY004 Demyelinating Disease 57 0.040
178
MVM001 Movement Disease 49 0.040
179
PRD007 Periodontal Disease 65 0.039
180
CYT008 Cytomegalovirus Infection 60 0.039
181
OBS082 Obstructive Nephropathy 51 0.039
182
CRB008 Cerebral Atherosclerosis 41 0.039
183
ANS016 Anosmia 40 0.039
184
SBC016 Subacute Delirium 32 0.039
185
ACR006 Aceruloplasminemia 70 0.039
186
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 53 0.038
187
TTR001 Tetralogy of Fallot 71 0.038
188
CNG034 Congestive Heart Failure 68 0.038
189
EXF001 Exfoliation Syndrome 57 0.038
190
NRS003 Neurosyphilis 48 0.038
191
JVN024 Juvenile Hereditary Hemochromatosis 42 0.038
192
PRP030 Purpura 61 0.037
193
NMN002 Niemann-Pick Disease 61 0.037
194
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 55 0.037
195
INF032 Infertility 58 0.037
196
EXN002 Exanthem 56 0.037
197
GLM045 Glioma 55 0.037
198
TRP008 Tropical Calcific Pancreatitis 51 0.037
199
BRB001 Beriberi 45 0.037
200
c ATM017 Autoimmune Disease of the Nervous System 49 0.036
201
ATX038 Ataxia and Polyneuropathy, Adult-Onset 40 0.036
202
RST001 Restless Legs Syndrome 54 0.036
203
c CRD182 Ceroid Lipofuscinosis, Neuronal, 10 53 0.036
204
DYS021 Dysautonomia 45 0.036
205
CMM008 Communicating Hydrocephalus 38 0.035
206
ISC006 Ischemic Heart Disease 67 0.035
207
PRP016 Paraplegia 54 0.035
208
RTN016 Retinal Degeneration 53 0.035
209
CRB009 Cerebritis 37 0.035
210
c BLD140 Blood Group, I System 30 0.035
211
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 68 0.034
212
SPN301 Spinocerebellar Ataxia 2 59 0.034
213
ATM052 Autoimmune Disease 1 46 0.034
214
LNS003 Lens Disease 30 0.034
215
BRN028 Brain Cancer 74 0.034
216
OPT006 Optic Nerve Disease 60 0.034
217
CRN031 Cranial Nerve Disease 36 0.034
218
PRS040 Prostate Cancer 94 0.034
219
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 68 0.034
220
CNN005 Connective Tissue Disease 64 0.034
221
MYP004 Myopathy 63 0.034
222
NRC002 Narcolepsy 59 0.034
223
MCR010 Microcephaly 55 0.034
224
GNT033 Genetic Prion Diseases 30 0.034
225
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 47 0.033
226
SPN041 Spinal Cord Disease 52 0.033
227
c HNT010 Huntington Disease-Like 1 48 0.033
228
TYS001 Tay-Sachs Disease 70 0.032
230
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 44 0.031
231
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 66 0.031
232
PLM033 Pulmonary Embolism 63 0.031
233
HMR039 Hemorrhage, Intracerebral 59 0.031
234
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.031
235
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.031
236
LMB024 Limbic Encephalitis 42 0.031
237
ISL119 Isolated Optic Neuritis 36 0.031
238
OST012 Osteoarthritis 81 0.031
239
CRB087 Cerebral Arteriosclerosis 21 0.031
240
DYS154 Dystonia 65 0.030
241
PRP019 Peripheral Nervous System Disease 62 0.030
242
TRN015 Transient Cerebral Ischemia 58 0.030
243
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 57 0.030
244
BRX001 Bruxism 53 0.030
245
AST007 Astrocytoma 49 0.030
246
ADS004 Aids Dementia Complex 44 0.030
247
ALX002 Alexithymia 41 0.030
248
STR001 Striatonigral Degeneration 33 0.030
249
FXF002 Fox-Fordyce Disease 30 0.030
250
MTR031 Motor Neuro-Ophthalmic Disorders 17 0.030
251
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 61 0.030
252
FTL002 Fatal Familial Insomnia 46 0.030
253
FRG010 Fragile X Tremor/ataxia Syndrome 42 0.030
254
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 26 0.030
255
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.029
256
GLC009 Glucosephosphate Dehydrogenase Deficiency 51 0.029
257
RTN023 Retinitis 48 0.029
258
AYM001 Ayme-Gripp Syndrome 40 0.029
259
BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.027
260
LVR013 Liver Disease 75 0.027
261
LKM062 Leukemia, Acute Lymphoblastic 68 0.027
262
HMT002 Hematologic Cancer 62 0.027
263
LYM031 Lymphocytic Leukemia 61 0.027
264
HPT019 Hepatic Encephalopathy 60 0.027
265
NTR005 Nutritional Deficiency Disease 58 0.027
266
ALX003 Alexander Disease 58 0.027
267
RGH009 Right Atrial Isomerism 54 0.027
268
OST097 Osteoporotic Fracture 44 0.027
269
EPD070 Epidermoid Cysts 43 0.027
270
c BDY019 Body Mass Index Quantitative Trait Locus 18 42 0.027
271
c BDY020 Body Mass Index Quantitative Trait Locus 19 41 0.027
272
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.027
273
CRB059 Cerebellar Degeneration 40 0.027
274
c BDY011 Body Mass Index Quantitative Trait Locus 10 40 0.027
275
MYC088 Mycobacterium Avium Complex Infections 33 0.027
276
AND005 Androgen Insensitivity Syndrome, Mild 22 0.027
277
FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 50 0.027
278
PHN003 Phenylketonuria 73 0.026
279
CNN003 Conn\'s Syndrome 73 0.026
280
LYM017 Lyme Disease 71 0.026
281
WLS001 Wilson Disease 70 0.026
282
FRG001 Fragile X Syndrome 70 0.026
283
PSR002 Psoriasis 66 0.026
284
MSC005 Muscular Dystrophy 66 0.026
285
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.026
286
OPT009 Optic Neuritis 53 0.026
287
ATN002 Autonomic Nervous System Disease 49 0.026
288
MHR001 Mohr-Tranebjaerg Syndrome 45 0.026
289
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 41 0.026
290
EXC002 Exocrine Pancreatic Insufficiency 40 0.026
291
c PRG011 Progressive Myoclonus Epilepsy 40 0.026
292
c PRK085 Parkinson Disease 1, Autosomal Dominant 35 0.026
293
PRS013 Prosopagnosia 35 0.026
294
MYC026 Myoclonus Epilepsy 34 0.026
295
NRX001 Neuroaxonal Dystrophy 32 0.026
296
MYL069 Myeloma, Multiple 85 0.026
297
c HYP595 Hypertension, Essential 78 0.026
298
CRP001 Carpal Tunnel Syndrome 71 0.026
299
WRN001 Werner Syndrome 70 0.026
300
ADN018 Adenoma 64 0.026
301
ADR007 Adrenoleukodystrophy 72 0.024
302
FRD012 Friedreich Ataxia 1 67 0.024
303
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 62 0.024
304
NRD007 Neurodegeneration with Brain Iron Accumulation 48 0.024
305
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 42 0.024
306
SWL001 Swallowing Disorders 34 0.024
307
LNG032 Lung Cancer 99 0.022
308
HYP607 Hypercholesterolemia, Familial 81 0.022
309
SYS005 Systemic Scleroderma 69 0.022
310
THL005 Thalassemia 65 0.022
311
ALP009 Alopecia Areata 64 0.022
312
WLL001 Williams-Beuren Syndrome 63 0.022
313
ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.022
314
ANT006 Antiphospholipid Syndrome 60 0.022
315
PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.022
316
c MYT020 Myotonic Dystrophy 2 55 0.022
317
HYP005 Hypokalemia 55 0.022
318
XRD022 Xeroderma Pigmentosum, Complementation Group D 54 0.022
319
c ART119 Arthrogryposis, Distal, Type 5 54 0.022
320
RTN209 Retinoschisis 1, X-Linked, Juvenile 53 0.022
321
HYP080 Hypogonadism 52 0.022
322
WDH003 Woodhouse-Sakati Syndrome 52 0.022
323
PLS009 Plasma Cell Neoplasm 49 0.022
324
HYP781 Hypoascorbemia 48 0.022
325
RNP003 Renpenning Syndrome 1 48 0.022
326
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 43 0.022
327
CHR008 Choroiditis 42 0.022
328
END072 Endotheliitis 40 0.022
329
NRR001 Neuroretinitis 39 0.022
330
c BDY005 Body Mass Index Quantitative Trait Locus 9 33 0.022
331
c BDY015 Body Mass Index Quantitative Trait Locus 12 32 0.022
332
c BDY010 Body Mass Index Quantitative Trait Locus 4 31 0.022
333
c BDY006 Body Mass Index Quantitative Trait Locus 8 31 0.022
334
c BDY012 Body Mass Index Quantitative Trait Locus 7 31 0.022
335
CRB031 Cerebral Arterial Disease 28 0.022
336
DSR011 Disorganization, Mouse, Homolog of 23 0.022
337
SGM006 Segmental Odontomaxillary Dysplasia 21 0.022
338
SBC025 Subcortical Arteriosclerotic Encephalopathy 20 0.022
339
NRL016 Neural Tube Defects 79 0.021
340
SRC014 Sarcoma 70 0.021
341
LNG099 Lung Disease 67 0.021
342
VSC011 Vasculitis 66 0.021
343
SPN186 Spinal Cord Injury 65 0.021
344
MNK001 Menkes Disease 64 0.021
345
GLL022 Guillain-Barre Syndrome 63 0.021
346
CHR071 Charcot-Marie-Tooth Disease 62 0.021
347
RHM027 Rheumatic Disease 61 0.021
348
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 0.021
349
KRN002 Kearns-Sayre Syndrome 61 0.021
350
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 59 0.021
351
LKN001 Leukoencephalopathy with Vanishing White Matter 57 0.021
352
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 56 0.021
353
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 55 0.021
354
OCL069 Ocular Motor Apraxia 55 0.021
355
MTC133 Mitochondrial Myopathy 54 0.021
356
NRL018 Neural Tube Defects, Folate-Sensitive 53 0.021
357
RTN003 Retinal Ischemia 52 0.021
358
PRN001 Purine Nucleoside Phosphorylase Deficiency 52 0.021
359
DNT005 Dentatorubral-Pallidoluysian Atrophy 52 0.021
360
HMS001 Hemosiderosis 52 0.021
361
GRS011 Gerstmann-Straussler Disease 51 0.021
362
c OPT053 Optic Atrophy 1 51 0.021
363
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 50 0.021
364
OVR063 Overnutrition 48 0.021
365
c PRM092 Primary Lateral Sclerosis, Adult, 1 47 0.021
366
c EPL027 Epileptic Encephalopathy, Early Infantile, 4 37 0.021
367
SCL056 Sclerosing Cholangitis, Neonatal 36 0.021
368
HRT007 Heart Cancer 36 0.021
369
c EPL026 Epileptic Encephalopathy, Early Infantile, 3 36 0.021
370
PRR004 Preretinal Fibrosis 33 0.021
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