Search results for (neurodegenerative OR senile) AND Alzheimer

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

# Family MCID Name MIFTS Score
1
c ALZ034 Alzheimer Disease 88 8.715
2
DMN031 Dementia, Lewy Body 68 1.882
3
DRL001 Dural Sinus Malformation 23 0.723
4
DMN002 Dementia 69 0.707
5
AGN016 Aging 63 0.342
6
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.319
7
VSC002 Vascular Dementia 58 0.314
8
c AMY004 Amyloidosis 69 0.287
9
c ENC018 Encephalopathy 65 0.274
10
c FRN006 Frontotemporal Dementia 69 0.222
11
c CTR002 Cataract 58 0.208
12
P ALZ049 Alzheimer Disease 2 61 0.204
13
P CNT035 Central Nervous System Disease 65 0.196
14
c PRK057 Parkinson Disease, Late-Onset 77 0.185
15
DPR016 Depression 73 0.176
17
c OST002 Osteoporosis 74 0.170
18
DWN001 Down Syndrome 72 0.168
19
c SPR120 Supranuclear Palsy, Progressive, 1 71 0.161
20
c TRC086 Trichohepatoenteric Syndrome 1 61 0.142
21
CRT072 Creutzfeldt-Jakob Disease 68 0.131
22
BNS003 Binswanger's Disease 47 0.128
23
APH002 Aphasia 60 0.123
24
PCK003 Pick Disease of Brain 66 0.123
25
c DBT009 Diabetes Mellitus 67 0.123
26
c TRM003 Tremor 56 0.123
28
APR001 Apraxia 54 0.118
29
MVM001 Movement Disease 67 0.118
30
c SCH015 Schizophrenia 73 0.117
31
CRB039 Cerebrovascular Disease 70 0.117
32
c EPL164 Epilepsy 73 0.113
33
c HYD006 Hydrocephalus 66 0.113
34
P ALZ054 Alzheimer Disease 4 47 0.110
35
VSC007 Vascular Disease 72 0.104
36
P ESS001 Essential Tremor 59 0.103
37
SCR011 Scrapie 42 0.100
38
P ALZ045 Alzheimer Disease 9 24 0.098
39
MLT157 Multiple System Atrophy 1 73 0.098
40
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.097
41
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.095
42
BSL008 Basal Ganglia Disease 49 0.095
43
DSS008 Disease of Mental Health 70 0.092
44
CHR073 Choreatic Disease 50 0.091
45
P ALZ056 Alzheimer Disease 3 49 0.090
46
c NRP001 Neuropathy 63 0.086
47
MTR014 Motor Neuron Disease 60 0.084
48
ALZ029 Alzheimer Disease Mitochondrial 28 0.084
49
P AMY091 Amyotrophic Lateral Sclerosis 1 90 0.082
50
BRN071 Brain Injury 54 0.082
51
c HNT016 Huntington Disease 74 0.081
52
ANX010 Anxiety 73 0.080
53
PST086 Posterior Cortical Atrophy 39 0.080
54
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.078
55
c LTR001 Lateral Sclerosis 60 0.078
56
SNL009 Senile Plaque Formation 27 0.075
57
RTN023 Retinitis 48 0.075
58
SPS003 Spastic Diplegia 49 0.075
59
BLL006 Bullous Pemphigoid 65 0.075
60
c OPN001 Open-Angle Glaucoma 53 0.074
61
PRN023 Prion Disease 53 0.072
62
SMN008 Semantic Dementia 54 0.072
63
P ALZ062 Alzheimer Disease 19 22 0.072
65
ANR007 Anorexia Nervosa 68 0.072
66
ACN002 Acanthosis Nigricans 65 0.072
67
c ANR048 Aniridia 1 63 0.072
68
ATX010 Ataxia Neuropathy Spectrum 39 0.072
69
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.072
70
c ACT232 Acute Necrotizing Encephalopathy 30 0.072
71
BLD137 Blood Group--Ahonen 21 0.072
72
c HRT032 Heart Disease 76 0.071
73
c NRV007 Nervous System Disease 72 0.070
74
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.070
75
c MLT020 Multiple Sclerosis 76 0.070
76
c ATX030 Ataxia-Telangiectasia 83 0.070
77
TRM010 Traumatic Brain Injury 56 0.069
78
INC002 Inclusion Body Myositis 64 0.068
79
c CRB088 Cerebral Atrophy 42 0.067
80
SPS057 Spasticity 44 0.067
81
KR002 Kuru 41 0.066
82
ERL001 Early Myoclonic Encephalopathy 53 0.066
83
P GLC092 Glaucoma, Primary Open Angle 58 0.065
84
PTL001 Patulous Eustachian Tube 31 0.065
85
THR013 Thoracic Outlet Syndrome 57 0.065
86
MNT002 Mental Depression 65 0.064
87
CRT033 Corticobasal Degeneration 53 0.064
88
HDN002 Head Injury 52 0.063
89
c ANG001 Angelman Syndrome 65 0.062
90
P ALZ032 Alzheimer Disease 18 18 0.061
91
ISC004 Ischemia 67 0.060
92
P SPN225 Spondyloarthropathy 1 76 0.060
93
STR067 Stroke, Ischemic 84 0.060
94
c AGN002 Agnosia 62 0.060
95
c BPL003 Bipolar Disorder 61 0.060
96
PNN005 Panencephalitis, Subacute Sclerosing 47 0.060
97
P ALZ015 Alzheimer Disease 6 24 0.059
98
INS024 Insulin-Like Growth Factor I 83 0.059
99
CPG001 Capgras Syndrome 23 0.059
100
MLT112 Multiloculated Renal Cyst 18 0.059
101
HYD061 Hydrocephalus, Normal-Pressure 52 0.057
102
c PNM007 Pneumonia 72 0.057
103
c TTR001 Tetralogy of Fallot 71 0.057
104
c RTN016 Retinal Degeneration 56 0.057
105
RMS001 Rem Sleep Behavior Disorder 45 0.055
106
c RTN008 Retinitis Pigmentosa 79 0.055
107
c CRD246 Cardiovascular System Disease 57 0.055
108
P LBR014 Leber Congenital Amaurosis 4 55 0.055
109
KRT002 Keratomalacia 51 0.055
110
c MYC033 Myoclonus 46 0.054
111
P NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.054
112
GRS011 Gerstmann-Straussler Disease 54 0.054
113
AND002 Androgen Insensitivity Syndrome 62 0.053
114
c AXN002 Axenfeld-Rieger Syndrome 62 0.053
115
ALR002 Al-Raqad Syndrome 41 0.053
116
c ART021 Arteriosclerosis 61 0.053
117
c LKM002 Leukemia 72 0.052
118
c ENC004 Encephalitis 66 0.052
119
c MYP004 Myopathy 65 0.052
120
NTR005 Nutritional Deficiency Disease 60 0.052
121
SYN058 Synucleinopathy 44 0.052
122
ANS006 Anosognosia 37 0.052
123
P ALZ063 Alzheimer's Disease 1 34 0.052
124
ART140 Arteries, Anomalies of 67 0.050
125
CRB085 Cerebral Hemorrhage 46 0.049
126
SPS019 Spastic Paraparesis 35 0.048
127
ALZ052 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology 10 0.047
128
LNG099 Lung Disease 70 0.047
129
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 62 0.047
130
NRT004 Neuritis 58 0.047
131
SPN035 Spindle Cell Sarcoma 52 0.047
132
HYP266 Hypoxia 63 0.047
133
c NRB001 Neuroblastoma 73 0.046
134
c ATS308 Autosomal Dominant Cerebellar Ataxia 58 0.045
135
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.045
136
c ACR001 Aicardi-Goutieres Syndrome 63 0.044
137
P ACR116 Aicardi-Goutieres Syndrome 1 48 0.044
138
MDD011 Mood Disorder 65 0.043
139
SLP005 Sleep Disorder 60 0.042
140
c LKD001 Leukodystrophy 57 0.042
141
SPC010 Speech and Communication Disorders 51 0.042
142
ACT049 Acute Disseminated Encephalomyelitis 56 0.042
143
c CRN018 Coronary Artery Anomaly 74 0.040
144
GLC003 Glucose Intolerance 59 0.040
146
DMN026 Dementia Pugilistica 22 0.040
147
ATM095 Autoimmune Disease 68 0.039
148
HMC014 Homocysteinemia 52 0.039
149
CRB008 Cerebral Atherosclerosis 44 0.039
150
BRN080 Brain Ischemia 43 0.039
151
PRG033 Progressive Non-Fluent Aphasia 49 0.039
152
c CMM008 Communicating Hydrocephalus 37 0.039
153
ARG004 Argyria 24 0.039
154
c SLP006 Sleep Apnea 70 0.038
155
CRB033 Cerebral Degeneration 42 0.038
156
PST027 Postencephalitic Parkinson Disease 43 0.038
157
c PRS038 Personality Disorder 68 0.038
158
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.038
159
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.038
160
ART001 Arterial Tortuosity Syndrome 59 0.038
161
KHL003 Kohlschutter-Tonz Syndrome 49 0.038
162
P ALP106 Alport Syndrome 1, X-Linked 49 0.038
163
HPT082 Hepatic Adenomas, Familial 49 0.038
164
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.038
165
ADP007 Adie Pupil 43 0.038
166
HNM002 Hinman Syndrome 29 0.038
167
P CHR682 Chronic Bilirubin Encephalopathy 22 0.038
168
ACR006 Aceruloplasminemia 72 0.038
170
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.038
171
c HRP006 Herpes Simplex 71 0.037
172
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 55 0.037
173
c MYS005 Myositis 62 0.037
174
CYT008 Cytomegalovirus Infection 61 0.037
175
c CRN300 Coronary Heart Disease 1 62 0.036
176
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.036
177
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.035
178
CHL123 Chlamydia 66 0.035
179
P BLD140 Blood Group, I System 26 0.035
180
RTN018 Retinal Disease 58 0.034
181
PRM153 Primary Progressive Apraxia of Speech 21 0.034
182
BHV002 Behavioral Variant of Frontotemporal Dementia 41 0.034
183
c MJR001 Major Depressive Disorder 67 0.033
184
P CNG216 Congenital Hydrocephalus 56 0.033
185
DYS073 Dysphagia 53 0.033
186
LGH007 Leigh Syndrome 66 0.032
187
P HNT010 Huntington Disease-Like 1 50 0.032
188
ATX038 Ataxia and Polyneuropathy, Adult-Onset 41 0.032
189
OPT006 Optic Nerve Disease 60 0.032
190
c DYS021 Dysautonomia 49 0.032
191
c OLV001 Olivopontocerebellar Atrophy 49 0.032
192
P CRD182 Ceroid Lipofuscinosis, Neuronal, 10 47 0.032
193
NTR027 Neutrophil Actin Dysfunction 32 0.032
194
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 0.031
195
HMR039 Hemorrhage, Intracerebral 62 0.031
196
c ANT006 Antiphospholipid Syndrome 60 0.031
197
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.031
198
ADL002 Adult Syndrome 55 0.031
199
PRP016 Paraplegia 55 0.031
200
NRS003 Neurosyphilis 47 0.031
201
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.031
202
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.031
203
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 0.031
204
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.031
205
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 43 0.031
206
CHL147 Chlamydia Pneumonia 42 0.031
207
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.031
208
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.031
209
CRB009 Cerebritis 39 0.031
211
c MYT002 Myotonic Dystrophy 52 0.031
212
AST005 Asthma 81 0.031
213
c MYC007 Myocardial Infarction 78 0.031
214
HPT019 Hepatic Encephalopathy 60 0.031
215
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.031
216
ATM052 Autoimmune Disease 1 41 0.031
217
PSY004 Psychotic Disorder 74 0.030
218
c MSC005 Muscular Dystrophy 66 0.030
219
PRD007 Periodontal Disease 66 0.030
220
c MCR010 Microcephaly 59 0.030
221
c TMP001 Temporal Lobe Epilepsy 57 0.030
222
c GLM045 Glioma 56 0.030
224
CGN007 Cognitive Function 1, Social 32 0.030
225
CNN003 Conn's Syndrome 73 0.029
226
P NMN015 Niemann-Pick Disease, Type C1 68 0.029
227
PRT058 Pure Autonomic Failure 66 0.029
228
c NRC002 Narcolepsy 59 0.029
229
c DBT005 Diabetes Insipidus 55 0.029
230
c NMN002 Niemann-Pick Disease 50 0.029
231
SBC016 Subacute Delirium 34 0.029
232
c FRD012 Friedreich Ataxia 1 67 0.029
233
SND001 Sandhoff Disease 66 0.029
234
c SPN301 Spinocerebellar Ataxia 2 60 0.029
235
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.029
236
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.029
237
LNS003 Lens Disease 40 0.029
238
AYM001 Ayme-Gripp Syndrome 39 0.029
239
c RHM011 Rheumatoid Arthritis 82 0.027
240
c ART022 Arthritis 78 0.027
241
c ATR011 Atrial Fibrillation 69 0.027
242
HYP066 Hyperglycemia 65 0.027
243
PLM033 Pulmonary Embolism 64 0.027
244
ALX003 Alexander Disease 58 0.027
245
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.027
246
AMN003 Amnestic Disorder 53 0.027
247
RGH009 Right Atrial Isomerism 53 0.027
248
HYP081 Hypolipoproteinemia 49 0.027
249
HPT004 Hepatic Coma 45 0.027
250
ISL119 Isolated Optic Neuritis 34 0.027
251
MYC088 Mycobacterium Avium Complex Infections 34 0.027
252
P BDY005 Body Mass Index Quantitative Trait Locus 9 29 0.027
253
P BDY015 Body Mass Index Quantitative Trait Locus 12 28 0.027
254
P BDY010 Body Mass Index Quantitative Trait Locus 4 27 0.027
255
P BDY006 Body Mass Index Quantitative Trait Locus 8 27 0.027
256
P BDY012 Body Mass Index Quantitative Trait Locus 7 27 0.027
257
BLD153 Blood Group--Swann System 25 0.027
258
AND005 Androgen Insensitivity Syndrome, Mild 19 0.027
259
c TYS001 Tay-Sachs Disease 70 0.027
260
c RST001 Restless Legs Syndrome 60 0.027
261
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 56 0.027
262
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 46 0.027
263
c PRS040 Prostate Cancer 93 0.026
264
MLR004 Malaria 85 0.026
265
c FRG001 Fragile X Syndrome 70 0.026
266
P CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.026
267
c ATS364 Autism 68 0.026
268
P MCP050 Mucopolysaccharidosis, Type Ii 67 0.026
269
c PNC044 Pancreatitis 62 0.026
270
c EXN002 Exanthem 62 0.026
271
TRN015 Transient Cerebral Ischemia 59 0.026
272
ATN002 Autonomic Nervous System Disease 54 0.026
273
RTN020 Retinal Vascular Disease 54 0.026
274
OBS082 Obstructive Nephropathy 52 0.026
275
c PTY003 Pityriasis Rubra Pilaris 52 0.026
276
c AST007 Astrocytoma 51 0.026
277
TRP008 Tropical Calcific Pancreatitis 50 0.026
278
HPR003 Heparin-Induced Thrombocytopenia 49 0.026
279
ADS004 Aids Dementia Complex 45 0.026
280
MHR001 Mohr-Tranebjaerg Syndrome 44 0.026
281
BWN003 Bowenoid Papulosis 43 0.026
282
P PRS136 Prostate Cancer, Hereditary, 6 40 0.026
283
P PRS130 Prostate Cancer, Hereditary, 8 37 0.026
284
P PRK085 Parkinson Disease 1, Autosomal Dominant 32 0.026
285
OST012 Osteoarthritis 81 0.026
286
P HYP595 Hypertension, Essential 77 0.026
287
WRN001 Werner Syndrome 74 0.026
288
CRP001 Carpal Tunnel Syndrome 72 0.026
289
CNG034 Congestive Heart Failure 71 0.026
290
c TMP003 Temporal Arteritis 68 0.026
291
ADN018 Adenoma 65 0.026
292
RTN209 Retinoschisis 1, X-Linked, Juvenile 55 0.026
293
CRB087 Cerebral Arteriosclerosis 21 0.026
294
BRN028 Brain Cancer 74 0.024
295
ADR007 Adrenoleukodystrophy 72 0.024
296
SRC014 Sarcoma 70 0.024
297
APN008 Apnea, Obstructive Sleep 68 0.024
298
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.024
299
c CHR071 Charcot-Marie-Tooth Disease 65 0.024
300
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.024
301
c SLL003 Salla Disease 53 0.024
302
FTL002 Fatal Familial Insomnia 50 0.024
303
c NRD007 Neurodegeneration with Brain Iron Accumulation 49 0.024
304
P PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 47 0.024
305
FRG010 Fragile X Tremor/ataxia Syndrome 41 0.024
306
P CRD184 Ceroid Lipofuscinosis, Neuronal, 5 37 0.024
307
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 32 0.024
308
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.024
309
CLS047 Classic Progressive Supranuclear Palsy Syndrome 27 0.024
310
c LNG032 Lung Cancer 99 0.022
311
c HYP607 Hypercholesterolemia, Familial 82 0.022
312
c LVR013 Liver Disease 77 0.022
313
c NRF023 Neurofibromatosis, Type Ii 76 0.022
314
ISC006 Ischemic Heart Disease 72 0.022
315
P MYT021 Myotonic Dystrophy 1 72 0.022
316
c SYS005 Systemic Scleroderma 70 0.022
317
c LKM062 Leukemia, Acute Lymphoblastic 70 0.022
318
P ATR087 Atrial Standstill 1 69 0.022
319
c ALP009 Alopecia Areata 68 0.022
320
WLL001 Williams-Beuren Syndrome 64 0.022
321
HYP056 Hypoglycemia 64 0.022
322
HMT002 Hematologic Cancer 64 0.022
323
c LYM031 Lymphocytic Leukemia 61 0.022
324
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.022
325
EXF001 Exfoliation Syndrome 58 0.022
326
HYP005 Hypokalemia 56 0.022
327
OCL006 Ocular Hypertension 56 0.022
328
TLN003 Telangiectasis 55 0.022
329
c XRD022 Xeroderma Pigmentosum, Complementation Group D 54 0.022
330
c PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 52 0.022
331
RNP003 Renpenning Syndrome 1 52 0.022
332
P ART119 Arthrogryposis, Distal, Type 5 50 0.022
333
HYP781 Hypoascorbemia 49 0.022
334
NRR001 Neuroretinitis 48 0.022
335
CHR008 Choroiditis 44 0.022
336
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 43 0.022
337
LMB024 Limbic Encephalitis 43 0.022
338
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 43 0.022
339
c CRB059 Cerebellar Degeneration 40 0.022
340
BRK012 Broken Heart Syndrome 39 0.022
341
END072 Endotheliitis 39 0.022
342
OST097 Osteoporotic Fracture 36 0.022
343
c RTT002 Rett Syndrome 83 0.021
344
PHN003 Phenylketonuria 75 0.021
345
WLS001 Wilson Disease 71 0.021
346
LYM017 Lyme Disease 71 0.021
347
c PSR002 Psoriasis 67 0.021
348
CNN005 Connective Tissue Disease 67 0.021
349
c VSC011 Vasculitis 67 0.021
350
MSC157 Muscular Dystrophy, Duchenne Type 66 0.021
351
c DYS154 Dystonia 66 0.021
352
SPN186 Spinal Cord Injury 66 0.021
353
c PRP019 Peripheral Nervous System Disease 66 0.021
354
LPD008 Lipid Metabolism Disorder 65 0.021
355
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.021
356
MNK001 Menkes Disease 65 0.021
357
c GLL022 Guillain-Barre Syndrome 64 0.021
358
GT001 Gout 62 0.021
359
LKN001 Leukoencephalopathy with Vanishing White Matter 57 0.021
360
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.021
361
c OPT009 Optic Neuritis 55 0.021
362
P SPS222 Spastic Paraplegia 20, Autosomal Recessive 54 0.021
363
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.021
364
P OPT053 Optic Atrophy 1 54 0.021
365
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.021
366
BRX001 Bruxism 53 0.021
367
P PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 53 0.021
368
PLM017 Pulmonary Alveolar Microlithiasis 52 0.021
369
c MTC133 Mitochondrial Myopathy 52 0.021
370
OCL069 Ocular Motor Apraxia 51 0.021
371
NRL004 Neuroleptic Malignant Syndrome 51 0.021
372
P MTR002 Mitral Valve Insufficiency 50 0.021
373
P SPS128 Spastic Paraplegia 7, Autosomal Recessive 49 0.021
374
P CHR579 Chiari Malformation Type Ii 49 0.021
375
P PRM092 Primary Lateral Sclerosis, Adult, 1 47 0.021
376
MSS001 Masa Syndrome 47 0.021
377
HRT007 Heart Cancer 46 0.021
378
ICH020 Ichthyosis Prematurity Syndrome 45 0.021
379
ALX002 Alexithymia 43 0.021
380
BRB001 Beriberi 43 0.021
381
EXC002 Exocrine Pancreatic Insufficiency 42 0.021
382
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 41 0.021
383
P PRG011 Progressive Myoclonus Epilepsy 40 0.021
384
P EPL027 Epileptic Encephalopathy, Early Infantile, 4 38 0.021
385
c STR001 Striatonigral Degeneration 38 0.021
386
SCL056 Sclerosing Cholangitis, Neonatal 37 0.021
387
c MYC026 Myoclonus Epilepsy 36 0.021
388
NRX001 Neuroaxonal Dystrophy 35 0.021
389
c PRS013 Prosopagnosia 35 0.021
390
P EPL026 Epileptic Encephalopathy, Early Infantile, 3 34 0.021
391
PRK087 Parkinson-Dementia Syndrome 32 0.021
392
GNT033 Genetic Prion Diseases 30 0.021
393
RDN004 Radin Blood Group Antigen 29 0.021
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