Search results for supranuclear palsy

272 hits were found for supranuclear palsy

# Family MCID Name MIFTS Score
1
P SPR120 Supranuclear Palsy, Progressive, 1 70 13.095
2
PRK087 Parkinson-Dementia Syndrome 30 6.808
3
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 5.492
4
c SPR049 Supranuclear Palsy, Progressive, 2 19 4.217
5
c SPR048 Supranuclear Palsy, Progressive, 3 10 4.171
6
SPR038 Supranuclear Ocular Palsy 21 3.863
7
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 8 3.419
8
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 12 2.535
9
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.450
10
CRB009 Cerebritis 41 0.647
11
CRT033 Corticobasal Degeneration 51 0.448
12
SPS057 Spasticity 41 0.400
13
MLT157 Multiple System Atrophy 1 65 0.332
14
DMN002 Dementia 68 0.294
15
P ENC018 Encephalopathy 58 0.273
16
CRN031 Cranial Nerve Disease 45 0.258
17
P CRN035 Cranial Nerve Palsy 42 0.255
18
c CNT035 Central Nervous System Disease 65 0.254
19
BRN071 Brain Injury 54 0.253
20
MVM001 Movement Disease 40 0.251
21
P PRK057 Parkinson Disease, Late-Onset 78 0.246
22
OCL011 Ocular Motility Disease 31 0.243
23
MTR031 Motor Neuro-Ophthalmic Disorders 20 0.242
24
BSL008 Basal Ganglia Disease 44 0.242
25
P NRV007 Nervous System Disease 75 0.241
26
P NRP001 Neuropathy 63 0.232
27
P ALZ034 Alzheimer Disease 95 0.223
28
NRN002 Neuronitis 43 0.202
29
FRN006 Frontotemporal Dementia 70 0.199
30
AGN016 Aging 65 0.198
31
P DYS154 Dystonia 61 0.191
32
PSD001 Pseudobulbar Palsy 35 0.173
33
APR001 Apraxia 52 0.167
34
APH002 Aphasia 58 0.167
35
CRT072 Creutzfeldt-Jakob Disease 65 0.162
36
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.161
37
PCK003 Pick Disease of Brain 66 0.160
38
P LTR001 Lateral Sclerosis 58 0.158
39
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.145
40
FCL012 Facial Paralysis 50 0.134
41
HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 27 0.132
42
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.131
43
INT042 Internuclear Ophthalmoplegia 40 0.131
44
DYS073 Dysphagia 47 0.131
45
P CRV039 Cervicitis 49 0.130
46
P MNN013 Meningitis 71 0.129
47
ANR040 Aneurysm 61 0.126
48
ACR006 Aceruloplasminemia 65 0.125
49
MTR014 Motor Neuron Disease 62 0.122
50
P LRY019 Laryngitis 57 0.119
51
KFR001 Kufor-Rakeb Syndrome 42 0.119
52
P SCL018 Scoliosis 56 0.117
53
P STR001 Striatonigral Degeneration 34 0.117
54
P LYM118 Lymphoma 71 0.117
55
MYC033 Myoclonus 40 0.115
56
P EPL164 Epilepsy 70 0.112
57
P ANR048 Aniridia 1 68 0.112
58
ANR038 Anorexia Nervosa 1 21 0.112
59
BLD137 Blood Group--Ahonen 17 0.112
60
RMS001 Rem Sleep Behavior Disorder 42 0.110
61
P PNM007 Pneumonia 70 0.109
62
P TRM003 Tremor 54 0.109
63
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.105
64
P PRS038 Personality Disorder 65 0.104
65
P CRB088 Cerebral Atrophy 38 0.104
66
P BLP003 Blepharospasm 46 0.104
67
P HYD006 Hydrocephalus 68 0.102
68
HMP005 Hemiplegia 54 0.102
69
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.097
70
RTN023 Retinitis 52 0.096
71
HRP004 Herpes Zoster 61 0.095
72
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.095
73
ANX010 Anxiety 72 0.094
74
NRL004 Neuroleptic Malignant Syndrome 44 0.094
75
ATN005 Autonomic Dysfunction 51 0.093
76
PRG033 Progressive Non-Fluent Aphasia 48 0.093
77
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 42 0.093
78
PNM010 Pneumothorax, Primary Spontaneous 41 0.093
79
SMN008 Semantic Dementia 41 0.093
80
OBS003 Obsessive-Compulsive Personality Disorder 29 0.093
81
ALR002 Al-Raqad Syndrome 30 0.092
82
GZP003 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 1 22 0.090
83
CNJ001 Conjugate Gaze Palsy 30 0.089
84
c ESS001 Essential Tremor 58 0.089
85
PRR007 Perry Syndrome 51 0.089
86
ASP007 Aspiration Pneumonia 49 0.089
87
NRS003 Neurosyphilis 44 0.088
88
c BRN108 Branchiootic Syndrome 1 47 0.087
89
MNT002 Mental Depression 60 0.086
90
SPC010 Speech and Communication Disorders 40 0.086
91
EXT022 Exotropia 41 0.085
92
c BLD140 Blood Group, I System 37 0.085
93
P ADN016 Adenocarcinoma 71 0.084
94
P BCL006 B-Cell Lymphomas 70 0.084
95
NRG002 Neurogenic Bladder 53 0.084
96
EST005 Esotropia 43 0.083
97
c GCH017 Gaucher Disease, Type Iii 47 0.083
98
P DYS021 Dysautonomia 47 0.083
99
SYN058 Synucleinopathy 42 0.083
100
c NMN015 Niemann-Pick Disease, Type C1 57 0.082
101
P TRT019 Torticollis 45 0.081
102
BNF002 Bone Fracture 56 0.080
103
MBS002 Moebius Syndrome 53 0.080
104
P ENC004 Encephalitis 66 0.079
105
ART016 Aortic Aneurysm 70 0.078
106
P HYP024 Hypoparathyroidism 55 0.078
107
SPC005 Speech Disorder 44 0.078
108
CLN006 Colonic Pseudo-Obstruction 36 0.078
109
P MLT020 Multiple Sclerosis 85 0.077
110
HPT082 Hepatic Adenomas, Familial 52 0.077
111
SWL001 Swallowing Disorders 36 0.077
112
c CRB095 Cerebral Palsy, Spastic Quadriplegic, 3 17 0.077
113
P SLP006 Sleep Apnea 65 0.075
114
HYP052 Hyperkalemic Periodic Paralysis 57 0.075
115
PNC056 Pineocytoma 49 0.075
116
CNV002 Conversion Disorder 42 0.075
117
IDM001 Ideomotor Apraxia 38 0.075
118
P PTS002 Ptosis 50 0.075
119
P SYP003 Syphilis 55 0.072
120
P MJR001 Major Depressive Disorder 70 0.072
121
P NMN002 Niemann-Pick Disease 68 0.072
122
P RTN016 Retinal Degeneration 56 0.072
123
RST001 Restless Legs Syndrome 54 0.072
124
BRN014 Bronchopneumonia 45 0.072
125
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.072
126
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.072
127
WRN005 Wrinkles 41 0.072
128
BSL009 Basal Ganglia Calcification 39 0.072
129
c NMN014 Niemann-Pick Disease, Type C2 34 0.072
130
ORM002 Oromandibular Dystonia 32 0.072
131
SBC014 Subclavian Steal Syndrome 31 0.072
132
PST027 Postencephalitic Parkinson Disease 30 0.072
133
c PRK071 Parkinson Disease 14, Autosomal Recessive 29 0.072
134
CGN007 Cognitive Function 1, Social 27 0.072
135
CLR132 Colorblindness, Partial, Deutan Series 25 0.072
136
BRN097 Brainstem Auditory Evoked Responses 24 0.072
137
PRM153 Primary Progressive Apraxia of Speech 21 0.072
138
SPS134 Spasmodic Dystonia 20 0.072
139
OGL001 Ogilvie Syndrome 20 0.072
140
APR010 Apraxia of Eyelid Opening 17 0.072
141
HDN002 Head Injury 48 0.071
142
NRD027 Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy, Childhood-Onset 18 0.071
143
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.069
144
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.069
145
CHR073 Choreatic Disease 40 0.069
146
BLD163 Blood Group, Dombrock System 23 0.069
147
c SCN006 Secondary Syphilis 40 0.066
148
SPN331 Spondyloocular Syndrome 34 0.066
149
SPS019 Spastic Paraparesis 33 0.066
150
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.066
151
P RNG031 Ring Chromosome Y Syndrome 29 0.066
152
MLL002 Miller Fisher Syndrome 44 0.065
153
BRW001 Brown-Vialetto-Van Laere Syndrome 27 0.065
154
ALP046 Alport Syndrome, X-Linked 74 0.063
155
TTN003 Tetanus 65 0.063
156
NRM005 Neuromuscular Disease 60 0.063
157
HYD061 Hydrocephalus, Normal-Pressure 47 0.063
158
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 31 0.063
159
P MCH002 Machado-Joseph Disease 63 0.062
160
P HMN010 Hemangioma 61 0.060
161
P NRC002 Narcolepsy 64 0.059
162
CTR172 Citrullinemia, Classic 58 0.059
163
c SPN294 Spinocerebellar Ataxia 1 58 0.059
164
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.059
165
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 50 0.059
166
c SPL067 Split-Hand/foot Malformation 1 40 0.059
167
c MYP021 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 37 0.059
168
c SPS203 Spastic Paraplegia 78, Autosomal Recessive 27 0.059
169
c SPS072 Spastic Ataxia 1, Autosomal Dominant 25 0.059
170
c PRK065 Parkinson Disease 20, Early-Onset 25 0.059
171
CHR158 Charles Bonnet Syndrome 23 0.059
172
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 18 0.059
173
CRB007 Cerebral Sarcoidosis 15 0.059
174
P MYP006 Myopia 56 0.057
175
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.057
176
c TRC078 Trichohepatoenteric Syndrome 2 34 0.057
177
P RSP003 Respiratory Failure 71 0.054
178
CRB039 Cerebrovascular Disease 68 0.054
179
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.054
180
P KRT007 Keratoconus 49 0.054
181
P KRN004 Kernicterus 48 0.054
182
IDP070 Idiopathic Scoliosis 42 0.054
183
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 33 0.054
184
OST006 Osteoblastoma 32 0.054
185
P NRM001 Neuromyelitis Optica 67 0.051
186
LSC001 Lesch-Nyhan Syndrome 62 0.051
187
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.051
188
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.051
189
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.051
190
WRN002 Wernicke-Korsakoff Syndrome 52 0.051
191
GNG005 Gangliocytoma 50 0.051
192
ESN006 Eosinophilic Meningitis 38 0.051
193
c SRC023 Sarcoidosis 2 30 0.051
194
c ATS307 Autosomal Recessive Cerebellar Ataxia 27 0.051
195
AND005 Androgen Insensitivity Syndrome, Mild 16 0.051
196
P OST002 Osteoporosis 75 0.047
197
DMN031 Dementia, Lewy Body 66 0.047
198
P GCH001 Gaucher's Disease 62 0.047
199
P EPS003 Episodic Ataxia 57 0.047
200
c EPS035 Episodic Ataxia, Type 2 54 0.047
201
SPN041 Spinal Cord Disease 54 0.047
202
P OLV001 Olivopontocerebellar Atrophy 51 0.047
203
CVR006 Cavernous Hemangioma 48 0.047
204
MTS001 Mutism 42 0.047
205
ADP007 Adie Pupil 41 0.047
206
c AMY069 Amyotrophic Lateral Sclerosis 21 39 0.047
207
AGR018 Agraphia 38 0.047
208
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.047
209
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 35 0.047
210
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 35 0.047
211
c NRM008 Neuromyelitis Optica Spectrum Disorder 30 0.047
212
VST003 Vestibular Nystagmus 28 0.047
213
FXC001 Foix Chavany Marie Syndrome 24 0.047
214
BLC018 Bile Acid Synthesis Defect, Congenital, 6 18 0.047
215
OST012 Osteoarthritis 88 0.041
216
PSY004 Psychotic Disorder 72 0.041
217
P MCL013 Mucolipidosis Iv 67 0.041
218
c ART101 Aortic Valve Disease 2 65 0.041
219
INC002 Inclusion Body Myositis 64 0.041
220
PRT058 Pure Autonomic Failure 60 0.041
221
c ALZ049 Alzheimer Disease 2 59 0.041
222
VSC002 Vascular Dementia 58 0.041
223
P SBS003 Substance Abuse 57 0.041
224
P ATR001 Atrioventricular Septal Defect 56 0.041
225
TXC002 Toxic Encephalopathy 55 0.041
226
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 54 0.041
227
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.041
228
c VRL007 Viral Encephalitis 53 0.041
229
ATN002 Autonomic Nervous System Disease 51 0.041
230
DSS008 Disease of Mental Health 51 0.041
231
c ERL020 Early-Onset Schizophrenia 51 0.041
232
CCN002 Cocaine Abuse 50 0.041
233
MGC001 Megacolon 50 0.041
234
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 49 0.041
235
AMN003 Amnestic Disorder 45 0.041
236
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.041
237
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.041
238
ALX001 Alexia 44 0.041
239
c ALZ054 Alzheimer Disease 4 43 0.041
240
TND006 Tendinosis 43 0.041
241
BNS003 Binswanger's Disease 43 0.041
242
IMP006 Impulse Control Disorder 43 0.041
243
DLS001 Delusional Disorder 41 0.041
244
c PRG001 Progressive Muscular Atrophy 41 0.041
245
KLV001 Kluver-Bucy Syndrome 41 0.041
246
BHV002 Behavioral Variant of Frontotemporal Dementia 41 0.041
247
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 40 0.041
248
P FML043 Familial Idiopathic Basal Ganglia Calcification 40 0.041
249
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.041
250
c ERL006 Early-Onset Familial Alzheimer Disease 38 0.041
251
c AMY067 Amyotrophic Lateral Sclerosis 18 38 0.041
252
PST086 Posterior Cortical Atrophy 38 0.041
253
GTP001 Gait Apraxia 38 0.041
254
c PRK090 Parkinson Disease 3, Autosomal Dominant 37 0.041
255
c ERL047 Early-Onset Parkinson Disease 36 0.041
256
NMN001 Nominal Aphasia 36 0.041
257
ECH002 Echolalia 35 0.041
258
P PRS013 Prosopagnosia 34 0.041
259
c PRK025 Parkinson Disease 10 33 0.041
260
LYS021 Loeys-Dietz Syndrome 3 33 0.041
261
AKN002 Akinetic Mutism 33 0.041
262
c SPN104 Spinocerebellar Ataxia 34 32 0.041
263
HYP572 Hypoganglionosis 31 0.041
264
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 30 0.041
265
SNL009 Senile Plaque Formation 26 0.041
266
c HRD173 Hereditary Late-Onset Parkinson Disease 26 0.041
267
EXP001 Expressive Language Disorder 24 0.041
268
ALC013 Alcohol-Induced Mental Disorder 23 0.041
269
WRT002 Writing Disorder 23 0.041
270
ARG004 Argyria 21 0.041
271
ASS001 Associative Agnosia 18 0.041
272
PHN002 Phonagnosia 18 0.041
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