Search results for (neurodegenerative OR senile) AND Alzheimer

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

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 87 8.685
2
DMN031 Dementia, Lewy Body 67 1.879
3
DMN002 Dementia 69 0.699
4
AGN016 Aging 63 0.341
5
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.315
6
VSC002 Vascular Dementia 57 0.312
7
P AMY004 Amyloidosis 64 0.286
8
P ENC018 Encephalopathy 65 0.271
9
P FRN006 Frontotemporal Dementia 69 0.227
10
P CTR002 Cataract 59 0.210
11
c ALZ049 Alzheimer Disease 2 60 0.202
12
c CNT035 Central Nervous System Disease 65 0.192
13
P PRK057 Parkinson Disease, Late-Onset 76 0.186
14
DPR016 Depression 72 0.177
15
P OST002 Osteoporosis 74 0.170
17
DWN001 Down Syndrome 71 0.166
18
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.160
19
P TRC086 Trichohepatoenteric Syndrome 1 60 0.139
20
CRT072 Creutzfeldt-Jakob Disease 67 0.134
21
BNS003 Binswanger's Disease 47 0.126
22
PCK003 Pick Disease of Brain 64 0.123
24
APH002 Aphasia 59 0.120
25
P TRM003 Tremor 55 0.119
26
P DBT009 Diabetes Mellitus 67 0.119
27
CRB039 Cerebrovascular Disease 70 0.118
28
P EPL164 Epilepsy 72 0.116
29
APR001 Apraxia 53 0.115
30
MVM001 Movement Disease 67 0.115
31
P SCH015 Schizophrenia 73 0.114
32
CHR073 Choreatic Disease 50 0.113
33
c ALZ054 Alzheimer Disease 4 50 0.112
34
P HYD006 Hydrocephalus 67 0.110
35
SCR011 Scrapie 43 0.103
36
VSC007 Vascular Disease 72 0.101
37
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.100
38
c ALZ056 Alzheimer Disease 3 53 0.100
39
c ESS001 Essential Tremor 59 0.100
40
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.098
41
c ALZ045 Alzheimer Disease 9 27 0.097
42
MLT157 Multiple System Atrophy 1 72 0.095
43
DSS008 Disease of Mental Health 71 0.094
44
STR067 Stroke, Ischemic 82 0.092
45
BSL008 Basal Ganglia Disease 48 0.092
46
P MCR115 Microvascular Complications of Diabetes 5 70 0.091
48
P NRP001 Neuropathy 63 0.087
49
MTR014 Motor Neuron Disease 60 0.084
50
BRN071 Brain Injury 55 0.084
51
P HNT016 Huntington Disease 73 0.083
52
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.080
53
ANX010 Anxiety 73 0.079
54
PST086 Posterior Cortical Atrophy 38 0.079
55
BLL006 Bullous Pemphigoid 64 0.078
56
SPS003 Spastic Diplegia 55 0.078
57
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.076
59
P LTR001 Lateral Sclerosis 60 0.076
60
P HRT032 Heart Disease 76 0.076
61
ALZ029 Alzheimer Disease Mitochondrial 27 0.075
62
SNL009 Senile Plaque Formation 26 0.074
63
GRS011 Gerstmann-Straussler Disease 56 0.074
64
RTN023 Retinitis 48 0.074
65
P ATX030 Ataxia-Telangiectasia 82 0.073
66
ANR007 Anorexia Nervosa 68 0.073
67
P ANR048 Aniridia 1 64 0.073
68
ACN002 Acanthosis Nigricans 64 0.073
69
ATX010 Ataxia Neuropathy Spectrum 39 0.073
70
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.073
71
P ACT232 Acute Necrotizing Encephalopathy 30 0.073
72
BLD137 Blood Group--Ahonen 24 0.073
73
PRN023 Prion Disease 54 0.072
74
P OPN001 Open-Angle Glaucoma 53 0.072
75
HPT019 Hepatic Encephalopathy 60 0.072
76
c ALZ062 Alzheimer Disease 19 24 0.072
77
c ALZ063 Alzheimer's Disease 1 40 0.072
78
TRM010 Traumatic Brain Injury 56 0.072
79
SMN008 Semantic Dementia 53 0.072
80
P MLT020 Multiple Sclerosis 75 0.071
81
P NRV007 Nervous System Disease 71 0.071
82
ERL001 Early Myoclonic Encephalopathy 53 0.069
83
PST027 Postencephalitic Parkinson Disease 43 0.069
84
INC002 Inclusion Body Myositis 63 0.067
85
P CRB088 Cerebral Atrophy 39 0.066
86
THR013 Thoracic Outlet Syndrome 56 0.066
87
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 44 0.066
88
SPS057 Spasticity 44 0.065
89
KR002 Kuru 40 0.065
90
HDN002 Head Injury 52 0.064
91
c GLC092 Glaucoma, Primary Open Angle 57 0.064
92
CRT033 Corticobasal Degeneration 58 0.064
93
P ANG001 Angelman Syndrome 64 0.064
94
MNT002 Mental Depression 65 0.063
95
c SPN225 Spondyloarthropathy 1 75 0.062
96
c ALZ015 Alzheimer Disease 6 24 0.061
97
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.060
98
ISC004 Ischemia 67 0.059
99
CNG034 Congestive Heart Failure 70 0.059
100
P AGN002 Agnosia 61 0.059
101
P BPL003 Bipolar Disorder 61 0.059
102
PNN005 Panencephalitis, Subacute Sclerosing 46 0.059
103
c ALZ032 Alzheimer Disease 18 18 0.058
104
INS024 Insulin-Like Growth Factor I 82 0.058
105
P ENC004 Encephalitis 66 0.058
106
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 53 0.057
107
c CNG216 Congenital Hydrocephalus 57 0.057
108
AND002 Androgen Insensitivity Syndrome 61 0.056
109
P AXN002 Axenfeld-Rieger Syndrome 57 0.056
110
ALR002 Al-Raqad Syndrome 40 0.056
111
HYD061 Hydrocephalus, Normal-Pressure 51 0.056
112
RTN209 Retinoschisis 1, X-Linked, Juvenile 57 0.056
113
P PNM007 Pneumonia 72 0.055
114
P TTR001 Tetralogy of Fallot 70 0.055
115
P RTN016 Retinal Degeneration 56 0.055
116
P PTY003 Pityriasis Rubra Pilaris 51 0.055
117
RMS001 Rem Sleep Behavior Disorder 44 0.054
118
P RTN008 Retinitis Pigmentosa 80 0.054
119
c LBR014 Leber Congenital Amaurosis 4 54 0.054
120
KRT002 Keratomalacia 51 0.054
121
P ACR001 Aicardi-Goutieres Syndrome 65 0.054
122
c ACR116 Aicardi-Goutieres Syndrome 1 50 0.054
123
P MYC033 Myoclonus 47 0.053
124
SPN035 Spindle Cell Sarcoma 53 0.052
125
PTL001 Patulous Eustachian Tube 31 0.052
126
P ART021 Arteriosclerosis 61 0.052
127
P LKM002 Leukemia 72 0.051
128
P MYP004 Myopathy 64 0.051
129
NTR005 Nutritional Deficiency Disease 59 0.051
130
CPG001 Capgras Syndrome 23 0.051
131
ART140 Arteries, Anomalies of 66 0.051
132
BHV002 Behavioral Variant of Frontotemporal Dementia 53 0.050
134
ANS006 Anosognosia 36 0.049
135
CRB085 Cerebral Hemorrhage 42 0.048
136
SPS019 Spastic Paraparesis 34 0.047
137
ALZ052 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology 10 0.047
138
VGN023 Vaginitis 58 0.046
139
HMC014 Homocysteinemia 53 0.046
140
LNG099 Lung Disease 70 0.046
141
c MCR129 Microvascular Complications of Diabetes 1 66 0.046
142
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 0.046
143
NRT004 Neuritis 58 0.046
144
TLN003 Telangiectasis 56 0.046
145
c MCR112 Microvascular Complications of Diabetes 2 42 0.046
146
HYP266 Hypoxia 63 0.045
147
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.043
148
P ATS308 Autosomal Dominant Cerebellar Ataxia 55 0.043
149
ACT049 Acute Disseminated Encephalomyelitis 56 0.043
150
P CRN018 Coronary Artery Anomaly 75 0.042
151
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.042
152
ART001 Arterial Tortuosity Syndrome 59 0.042
153
c ALP106 Alport Syndrome 1, X-Linked 53 0.042
154
c CHR682 Chronic Bilirubin Encephalopathy 33 0.042
155
DMN026 Dementia Pugilistica 23 0.042
156
MDD011 Mood Disorder 65 0.042
157
SLP005 Sleep Disorder 60 0.041
158
P LKD001 Leukodystrophy 57 0.041
159
P MYC007 Myocardial Infarction 78 0.041
160
NTR027 Neutrophil Actin Dysfunction 32 0.041
161
ATM095 Autoimmune Disease 68 0.040
162
ATX038 Ataxia and Polyneuropathy, Adult-Onset 42 0.040
163
GLC003 Glucose Intolerance 59 0.040
164
HMR039 Hemorrhage, Intracerebral 62 0.040
166
ACR006 Aceruloplasminemia 73 0.040
167
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.039
168
CRB008 Cerebral Atherosclerosis 44 0.039
169
BRN080 Brain Ischemia 43 0.039
170
SPC010 Speech and Communication Disorders 51 0.038
172
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.038
173
PRG033 Progressive Non-Fluent Aphasia 48 0.038
174
P CMM008 Communicating Hydrocephalus 38 0.038
175
ARG004 Argyria 24 0.038
176
P PRS038 Personality Disorder 67 0.037
177
KHL003 Kohlschutter-Tonz Syndrome 52 0.037
178
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.037
179
HPT082 Hepatic Adenomas, Familial 50 0.037
180
P JVN024 Juvenile Hereditary Hemochromatosis 44 0.037
181
ADP007 Adie Pupil 42 0.037
182
HNM002 Hinman Syndrome 31 0.037
183
P SLP006 Sleep Apnea 70 0.037
184
P FRD012 Friedreich Ataxia 1 66 0.037
185
CRB033 Cerebral Degeneration 41 0.037
186
P HRP006 Herpes Simplex 71 0.036
187
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 56 0.036
188
CYT008 Cytomegalovirus Infection 62 0.036
189
P MYS005 Myositis 61 0.036
190
PRT058 Pure Autonomic Failure 65 0.035
191
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.035
192
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.035
193
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 44 0.035
194
PRM153 Primary Progressive Apraxia of Speech 21 0.034
195
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.034
196
CHL123 Chlamydia 66 0.034
197
PRP016 Paraplegia 54 0.034
198
CHL147 Chlamydia Pneumonia 42 0.034
199
CRB009 Cerebritis 39 0.034
200
c BLD140 Blood Group, I System 29 0.034
201
OPT006 Optic Nerve Disease 60 0.033
202
RTN018 Retinal Disease 58 0.033
203
c HNT010 Huntington Disease-Like 1 50 0.033
204
P TMP001 Temporal Lobe Epilepsy 58 0.033
205
P MJR001 Major Depressive Disorder 67 0.033
206
P GLM045 Glioma 55 0.033
207
DYS073 Dysphagia 48 0.033
208
LGH007 Leigh Syndrome 67 0.031
209
P OLV001 Olivopontocerebellar Atrophy 48 0.031
210
c CRD182 Ceroid Lipofuscinosis, Neuronal, 10 47 0.031
211
P DYS021 Dysautonomia 45 0.031
212
P RHM011 Rheumatoid Arthritis 81 0.031
213
P ART022 Arthritis 77 0.031
214
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.031
215
P ANT006 Antiphospholipid Syndrome 60 0.031
216
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.031
217
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 55 0.031
218
ADL002 Adult Syndrome 55 0.031
219
AMN003 Amnestic Disorder 53 0.031
220
NRS003 Neurosyphilis 46 0.031
221
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 0.031
222
HPT004 Hepatic Coma 45 0.031
223
ASY002 Asymptomatic Neurosyphilis 43 0.031
224
c GLL037 Guillain-Barre Syndrome, Familial 39 0.031
225
ISL119 Isolated Optic Neuritis 34 0.031
226
BLD153 Blood Group--Swann System 25 0.031
227
OST012 Osteoarthritis 80 0.031
228
P CRN300 Coronary Heart Disease 1 61 0.031
229
P MYT002 Myotonic Dystrophy 52 0.031
230
LNS003 Lens Disease 40 0.031
231
c HYP595 Hypertension, Essential 81 0.031
232
AST005 Asthma 81 0.031
233
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.030
234
ATM052 Autoimmune Disease 1 40 0.030
235
P CLR023 Colorectal Cancer 99 0.029
236
PSY004 Psychotic Disorder 74 0.029
237
GLB002 Glioblastoma 74 0.029
238
P MSC005 Muscular Dystrophy 66 0.029
239
PRD007 Periodontal Disease 66 0.029
240
GLB015 Glioblastoma Multiforme 64 0.029
241
P MCR010 Microcephaly 55 0.029
242
HPR003 Heparin-Induced Thrombocytopenia 53 0.029
244
BLD165 Blood Group, Colton System 34 0.029
245
CGN007 Cognitive Function 1, Social 31 0.029
246
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.029
247
c NMN015 Niemann-Pick Disease, Type C1 67 0.029
248
P NMN002 Niemann-Pick Disease 61 0.029
249
P NRC002 Narcolepsy 59 0.029
250
P DBT005 Diabetes Insipidus 55 0.029
251
P CRB101 Cerebrooculofacioskeletal Syndrome 1 50 0.029
252
SBC016 Subacute Delirium 34 0.029
253
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.028
254
SND001 Sandhoff Disease 65 0.028
255
P SPN301 Spinocerebellar Ataxia 2 59 0.028
256
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 49 0.028
257
ADR022 Adrenomyeloneuropathy 43 0.028
258
P LNG032 Lung Cancer 99 0.027
259
HMN044 Human Immunodeficiency Virus Type 1 75 0.027
260
P BDY004 Body Mass Index Quantitative Trait Locus 11 72 0.027
261
ISC006 Ischemic Heart Disease 72 0.027
262
c ATR087 Atrial Standstill 1 70 0.027
263
P ATR011 Atrial Fibrillation 69 0.027
264
HYP066 Hyperglycemia 64 0.027
265
PLM033 Pulmonary Embolism 64 0.027
266
ALX003 Alexander Disease 58 0.027
267
RGH009 Right Atrial Isomerism 52 0.027
268
HYP081 Hypolipoproteinemia 49 0.027
269
BRN041 Bornholm Eye Disease 45 0.027
270
c BDY020 Body Mass Index Quantitative Trait Locus 19 44 0.027
271
c BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.027
272
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.027
273
c BDY006 Body Mass Index Quantitative Trait Locus 8 41 0.027
274
c BDY012 Body Mass Index Quantitative Trait Locus 7 41 0.027
275
c BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.027
276
c BDY005 Body Mass Index Quantitative Trait Locus 9 35 0.027
277
MYC088 Mycobacterium Avium Complex Infections 33 0.027
278
c BDY010 Body Mass Index Quantitative Trait Locus 4 32 0.027
279
c BDY015 Body Mass Index Quantitative Trait Locus 12 32 0.027
280
c BDY021 Body Mass Index Quantitative Trait Locus 20 30 0.027
281
AND005 Androgen Insensitivity Syndrome, Mild 21 0.027
282
SRC014 Sarcoma 70 0.026
283
P TYS001 Tay-Sachs Disease 69 0.026
284
P RST001 Restless Legs Syndrome 59 0.026
285
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 48 0.026
286
P NRD007 Neurodegeneration with Brain Iron Accumulation 45 0.026
287
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 44 0.026
288
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 33 0.026
289
P PRS040 Prostate Cancer 93 0.025
290
MLR004 Malaria 84 0.025
291
CNN003 Conn's Syndrome 70 0.025
292
P FRG001 Fragile X Syndrome 69 0.025
293
P ATS364 Autism 67 0.025
294
c MCP050 Mucopolysaccharidosis, Type Ii 66 0.025
295
SPN186 Spinal Cord Injury 66 0.025
296
P PNC044 Pancreatitis 62 0.025
297
P EXN002 Exanthem 62 0.025
298
TRN015 Transient Cerebral Ischemia 59 0.025
299
ATN002 Autonomic Nervous System Disease 56 0.025
300
RTN020 Retinal Vascular Disease 54 0.025
301
OBS082 Obstructive Nephropathy 52 0.025
302
P AST007 Astrocytoma 52 0.025
303
P NRB010 Neuroblastoma 1 51 0.025
304
c MTR002 Mitral Valve Insufficiency 50 0.025
305
TRP008 Tropical Calcific Pancreatitis 50 0.025
306
ADS004 Aids Dementia Complex 45 0.025
307
MHR001 Mohr-Tranebjaerg Syndrome 44 0.025
308
BWN003 Bowenoid Papulosis 42 0.025
309
c PRS136 Prostate Cancer, Hereditary, 6 40 0.025
310
c PRS130 Prostate Cancer, Hereditary, 8 37 0.025
311
c PRK085 Parkinson Disease 1, Autosomal Dominant 36 0.025
312
GNT033 Genetic Prion Diseases 30 0.025
313
WRN001 Werner Syndrome 73 0.025
314
CRP001 Carpal Tunnel Syndrome 71 0.025
315
P TMP003 Temporal Arteritis 69 0.025
316
ADN018 Adenoma 64 0.025
317
CRB087 Cerebral Arteriosclerosis 22 0.025
318
PHN003 Phenylketonuria 74 0.023
319
BRN028 Brain Cancer 72 0.023
320
ADR007 Adrenoleukodystrophy 71 0.023
321
APN008 Apnea, Obstructive Sleep 68 0.023
322
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.023
323
P CHR071 Charcot-Marie-Tooth Disease 65 0.023
324
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 62 0.023
325
DNT005 Dentatorubral-Pallidoluysian Atrophy 53 0.023
326
P SLL003 Salla Disease 52 0.023
327
FTL002 Fatal Familial Insomnia 51 0.023
328
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 48 0.023
329
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.023
330
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 39 0.023
331
SCL056 Sclerosing Cholangitis, Neonatal 37 0.023
332
CLS047 Classic Progressive Supranuclear Palsy Syndrome 28 0.023
333
P HYP607 Hypercholesterolemia, Familial 81 0.022
334
GST053 Gastric Cancer 78 0.022
335
P LVR013 Liver Disease 76 0.022
336
P NRF023 Neurofibromatosis, Type Ii 75 0.022
337
P DLT002 Dilated Cardiomyopathy 75 0.022
338
c MYT021 Myotonic Dystrophy 1 71 0.022
339
P LKM062 Leukemia, Acute Lymphoblastic 68 0.022
340
P SYS005 Systemic Scleroderma 67 0.022
341
P ALP009 Alopecia Areata 66 0.022
342
ACQ007 Acquired Immunodeficiency Syndrome 66 0.022
343
HYP056 Hypoglycemia 64 0.022
344
HMT002 Hematologic Cancer 64 0.022
345
WLL001 Williams-Beuren Syndrome 63 0.022
346
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 61 0.022
347
P LYM031 Lymphocytic Leukemia 61 0.022
348
EXF001 Exfoliation Syndrome 57 0.022
349
OCL006 Ocular Hypertension 56 0.022
350
HYP005 Hypokalemia 55 0.022
351
P XRD022 Xeroderma Pigmentosum, Complementation Group D 55 0.022
352
RNP003 Renpenning Syndrome 1 53 0.022
353
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 52 0.022
354
HYP781 Hypoascorbemia 50 0.022
355
NRR001 Neuroretinitis 47 0.022
356
c ART155 Arthrogryposis, Distal, Type 2b1 47 0.022
357
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 46 0.022
358
CHR008 Choroiditis 44 0.022
359
LMB024 Limbic Encephalitis 42 0.022
360
P CRB059 Cerebellar Degeneration 40 0.022
361
END072 Endotheliitis 39 0.022
362
BRK012 Broken Heart Syndrome 39 0.022
363
OST097 Osteoporotic Fracture 36 0.022
364
MTC135 Mitochondrial Import-Stimulating Factor 18 0.022
365
P RTT002 Rett Syndrome 82 0.020
366
WLS001 Wilson Disease 70 0.020
367
LYM017 Lyme Disease 70 0.020
368
P PSR002 Psoriasis 67 0.020
369
CNN005 Connective Tissue Disease 67 0.020
370
P GLL022 Guillain-Barre Syndrome 66 0.020
371
P VSC011 Vasculitis 66 0.020
372
P PRP019 Peripheral Nervous System Disease 66 0.020
373
LPD008 Lipid Metabolism Disorder 65 0.020
374
P DYS154 Dystonia 65 0.020
375
MSC157 Muscular Dystrophy, Duchenne Type 65 0.020
376
MNK001 Menkes Disease 64 0.020
377
GT001 Gout 62 0.020
378
P INF032 Infertility 60 0.020
379
c THY109 Thyroid Cancer, Nonmedullary, 1 59 0.020
380
LBR002 Leber Hereditary Optic Neuropathy 58 0.020
381
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.020
382
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 56 0.020
383
P OPT009 Optic Neuritis 55 0.020
384
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.020
385
c OPT053 Optic Atrophy 1 55 0.020
386
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 53 0.020
387
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 53 0.020
388
PRN001 Purine Nucleoside Phosphorylase Deficiency 52 0.020
389
NRL004 Neuroleptic Malignant Syndrome 52 0.020
390
P MTC133 Mitochondrial Myopathy 52 0.020
391
PLM017 Pulmonary Alveolar Microlithiasis 52 0.020
392
BRX001 Bruxism 51 0.020
393
OCL069 Ocular Motor Apraxia 49 0.020
394
c CHR579 Chiari Malformation Type Ii 49 0.020
395
c PRM092 Primary Lateral Sclerosis, Adult, 1 48 0.020
396
MSS001 Masa Syndrome 47 0.020
397
P BRB001 Beriberi 46 0.020
398
ICH020 Ichthyosis Prematurity Syndrome 45 0.020
399
ALX002 Alexithymia 43 0.020
400
SPN331 Spondyloocular Syndrome 41 0.020
401
EXC002 Exocrine Pancreatic Insufficiency 41 0.020
402
c EPL027 Epileptic Encephalopathy, Early Infantile, 4 40 0.020
403
c PRG011 Progressive Myoclonus Epilepsy 40 0.020
404
P STR001 Striatonigral Degeneration 38 0.020
405
c EPL026 Epileptic Encephalopathy, Early Infantile, 3 36 0.020
406
P MYC026 Myoclonus Epilepsy 36 0.020
407
NRX001 Neuroaxonal Dystrophy 35 0.020
408
P PRS013 Prosopagnosia 35 0.020
409
DFN039 Deafness-Infertility Syndrome 34 0.020
410
PRK087 Parkinson-Dementia Syndrome 34 0.020
411
c PRK093 Parkinson Disease 8, Autosomal Dominant 33 0.020
412
P DFN349 Deafness, Nonsyndromic Sensorineural, Mitochondrial 32 0.020
413
RDN004 Radin Blood Group Antigen 28 0.020
414
MDS024 Mediastinal Endodermal Sinus Tumors 26 0.020
415
HRN028 Horns in Sheep 24 0.020
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