Search results for supranuclear palsy

257 hits were found for supranuclear palsy

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 59 10.678
2
SPR100 Supranuclear Palsy, Progressive Atypical 28 6.373
3
SPR038 Supranuclear Ocular Palsy 17 3.851
4
c SPR049 Supranuclear Palsy, Progressive, 2 24 3.663
5
c SPR048 Supranuclear Palsy, Progressive, 3 14 3.575
6
CLS047 Classic Progressive Supranuclear Palsy Syndrome 15 3.436
7
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 7 3.401
8
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 9 2.493
9
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.437
10
c PRG046 Progressive Supranuclear Palsy, Mapt-Related 5 2.422
11
CRB037 Cerebral Palsy 54 0.635
12
CRB009 Cerebritis 39 0.620
13
P CRT033 Corticobasal Degeneration 46 0.449
14
P CRN035 Cranial Nerve Palsy 43 0.396
15
SPS057 Spasticity 42 0.374
16
MLT021 Multiple System Atrophy 70 0.329
17
DMN002 Dementia 52 0.288
18
c CNT035 Central Nervous System Disease 60 0.256
19
P NRV007 Nervous System Disease 70 0.252
20
CRN031 Cranial Nerve Disease 41 0.250
21
BSL008 Basal Ganglia Disease 44 0.234
22
EYD002 Eye Disease 57 0.234
23
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.233
24
MVM001 Movement Disease 52 0.232
25
NRN002 Neuronitis 39 0.194
26
P DYS154 Dystonia 61 0.172
27
c MLT009 Multiple Cranial Nerve Palsy 34 0.170
28
APR001 Apraxia 49 0.165
29
PSD001 Pseudobulbar Palsy 32 0.159
30
APH002 Aphasia 55 0.159
31
OCL011 Ocular Motility Disease 38 0.153
32
P ATX004 Ataxia 52 0.143
33
CRT072 Creutzfeldt-Jakob Disease 62 0.139
34
P LTR001 Lateral Sclerosis 53 0.133
35
P CRB042 Cerebellar Ataxia 69 0.128
36
MSC004 Muscle Tissue Disease 37 0.127
37
P MSC033 Muscle Disorders 52 0.124
38
PCK002 Pick Disease 68 0.119
39
HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 27 0.117
40
DYS073 Dysphagia 47 0.115
41
PHY002 Physical Disorder 43 0.114
42
KFR001 Kufor-Rakeb Syndrome 42 0.111
43
P ALZ034 Alzheimer Disease 76 0.111
44
PNM010 Pneumothorax, Primary Spontaneous 33 0.111
45
P CRV039 Cervicitis 45 0.110
46
INT042 Internuclear Ophthalmoplegia 37 0.109
47
P EPL164 Epilepsy 65 0.106
48
c PRK025 Parkinson Disease 10 40 0.105
49
SPC005 Speech Disorder 41 0.104
50
P TRM003 Tremor 53 0.103
51
P STR001 Striatonigral Degeneration 28 0.103
52
ANR040 Aneurysm 57 0.101
53
HMP005 Hemiplegia 50 0.101
54
PRG007 Progressive Bulbar Palsy 30 0.101
55
CRB033 Cerebral Degeneration 44 0.099
56
P CRB088 Cerebral Atrophy 39 0.099
57
MTR014 Motor Neuron Disease 56 0.098
58
P PNM007 Pneumonia 66 0.098
59
MTH009 Mouth Disease 62 0.098
60
P LRY019 Laryngitis 53 0.098
61
P MNN013 Meningitis 65 0.096
62
HRP004 Herpes Zoster 54 0.094
63
RMS001 Rem Sleep Behavior Disorder 40 0.094
64
c PRK045 Parkinson Disease 5 37 0.094
65
P LYM118 Lymphoma 69 0.093
66
CNJ001 Conjugate Gaze Palsy 28 0.092
67
BRT030 Birth Defects 44 0.089
68
c NMN015 Niemann-Pick Disease, Type C1 51 0.087
69
MNT002 Mental Depression 52 0.087
70
SMN008 Semantic Dementia 37 0.087
71
MYC033 Myoclonus 41 0.086
72
GZP003 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 1 20 0.085
73
NWC001 Newcastle Disease 51 0.084
74
c GCH017 Gaucher Disease, Type Iii 47 0.084
75
EYD001 Eye Degenerative Disease 32 0.084
76
PRR007 Perry Syndrome 58 0.082
77
SPC010 Speech and Communication Disorders 42 0.082
78
ALR002 Al-Raqad Syndrome 29 0.081
79
P HYD006 Hydrocephalus 66 0.081
80
MBS002 Moebius Syndrome 49 0.080
81
SPN369 Spinal Disease 38 0.079
82
c ESS001 Essential Tremor 58 0.079
83
BNF002 Bone Fracture 51 0.078
84
OPT006 Optic Nerve Disease 49 0.077
85
ADR009 Adrenal Cortex Disease 39 0.077
86
SWL001 Swallowing Disorders 32 0.077
87
P DMN033 Dementia, Frontotemporal 65 0.076
88
P PRS038 Personality Disorder 61 0.076
89
c PRK031 Parkinson Disease 1 51 0.076
90
P PLN008 Peeling Skin Syndrome 49 0.076
91
P DYS021 Dysautonomia 45 0.076
92
PRG033 Progressive Non-Fluent Aphasia 43 0.076
93
SYN058 Synucleinopathy 39 0.076
94
P ENC004 Encephalitis 61 0.075
95
ATN005 Autonomic Dysfunction 45 0.073
96
c NMN014 Niemann-Pick Disease, Type C2 37 0.073
97
OBS003 Obsessive-Compulsive Personality Disorder 37 0.073
98
c PRK071 Parkinson Disease 14, Autosomal Recessive 24 0.073
99
NRL004 Neuroleptic Malignant Syndrome 40 0.072
100
EXT022 Exotropia 39 0.071
101
AND005 Androgen Insensitivity Syndrome, Mild 16 0.071
102
ASP007 Aspiration Pneumonia 40 0.070
103
P PTS002 Ptosis 52 0.069
104
RTN023 Retinitis 49 0.069
105
HDN002 Head Injury 44 0.069
106
P BLP003 Blepharospasm 42 0.069
107
c CRB095 Cerebral Palsy, Spastic Quadriplegic, 3 17 0.065
108
P MCH002 Machado-Joseph Disease 62 0.063
109
EXF001 Exfoliation Syndrome 57 0.063
110
ADL002 Adult Syndrome 57 0.063
111
CSY001 C Syndrome 53 0.063
112
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 53 0.063
113
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 49 0.063
114
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 43 0.063
115
KHL003 Kohlschutter-Tonz Syndrome 42 0.063
116
NRM002 Normal Pressure Hydrocephalus 39 0.063
117
IDM001 Ideomotor Apraxia 36 0.063
118
c PLN021 Peeling Skin Syndrome 3 32 0.063
119
TTN003 Tetanus 60 0.063
120
HPT074 Hepatic Adenoma, Somatic 44 0.063
121
NRS003 Neurosyphilis 41 0.063
122
P ART022 Arthritis 72 0.060
123
ATN002 Autonomic Nervous System Disease 48 0.060
124
P OST012 Osteoarthritis 79 0.059
125
c SPN294 Spinocerebellar Ataxia 1 56 0.059
126
c PLN018 Peeling Skin Syndrome 2 43 0.059
127
c PRK059 Parkinson Disease 8 42 0.059
128
c PRK030 Parkinson Disease 4 41 0.059
129
TND006 Tendinosis 38 0.059
130
c SPS072 Spastic Ataxia 1, Autosomal Dominant 28 0.059
131
c PLN025 Peeling Skin Syndrome 5 25 0.059
132
c PRK065 Parkinson Disease 20, Early-Onset 25 0.059
133
c PRK022 Parkinson Disease 12 24 0.059
134
CHR158 Charles Bonnet Syndrome 20 0.059
135
TSY001 Tau Syndrome 12 0.059
136
P ADN016 Adenocarcinoma 69 0.058
137
P BCL006 B-Cell Lymphomas 64 0.058
138
P SYP003 Syphilis 51 0.058
139
c TRC078 Trichohepatoenteric Syndrome 2 34 0.058
140
CND002 Conduct Disorder 53 0.055
141
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 46 0.055
142
P KRN004 Kernicterus 45 0.055
143
ADT003 Auditory System Disease 41 0.055
144
c SCN006 Secondary Syphilis 39 0.055
145
SPC003 Specific Developmental Disorder 38 0.055
146
HNM002 Hinman Syndrome 27 0.055
147
P PRK057 Parkinson Disease, Late-Onset 68 0.051
148
ART016 Aortic Aneurysm 67 0.051
149
INC002 Inclusion Body Myositis 63 0.051
150
CRB039 Cerebrovascular Disease 63 0.051
151
LSC001 Lesch-Nyhan Syndrome 62 0.051
152
DMN031 Dementia, Lewy Body 59 0.051
153
P SZR006 Seizure Disorder 54 0.051
154
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.051
155
P HYP024 Hypoparathyroidism 52 0.051
156
GNG012 Gingival Overgrowth 51 0.051
157
P MTH007 Methemoglobinemia 44 0.051
158
MTS001 Mutism 41 0.051
159
P CRN026 Corneal Edema 39 0.051
160
SPS019 Spastic Paraparesis 34 0.051
161
CLN006 Colonic Pseudo-Obstruction 31 0.051
162
P GCH001 Gaucher's Disease 63 0.047
163
P OST002 Osteoporosis 63 0.047
164
MSC077 Muscle Eye Brain Disease 58 0.047
165
HMR039 Hemorrhage, Intracerebral 52 0.047
166
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.047
167
c PRK027 Parkinson Disease 15, Autosomal Recessive 47 0.047
168
WRN002 Wernicke-Korsakoff Syndrome 46 0.047
169
P CRN074 Coronary Artery Aneurysm 44 0.047
170
VST004 Vestibular Disease 43 0.047
171
BHV002 Behavioral Variant of Frontotemporal Dementia 41 0.047
172
DRG001 Drug Psychosis 41 0.047
173
CNV002 Conversion Disorder 40 0.047
174
BRN014 Bronchopneumonia 40 0.047
175
PNC056 Pineocytoma 39 0.047
176
BLD054 Blood Protein Disease 39 0.047
177
c PLN017 Peeling Skin Syndrome 1 38 0.047
178
GTP001 Gait Apraxia 36 0.047
179
AGR018 Agraphia 35 0.047
180
ADP007 Adie Pupil 35 0.047
181
c ERL047 Early-Onset Parkinson Disease 34 0.047
182
NMN001 Nominal Aphasia 33 0.047
183
c PLN024 Peeling Skin Syndrome 4 32 0.047
184
ECH002 Echolalia 30 0.047
185
c SNC002 Snca-Related Parkinson Disease 26 0.047
186
PST027 Postencephalitic Parkinson Disease 26 0.047
187
c HRD173 Hereditary Late-Onset Parkinson Disease 23 0.047
188
FXC001 Foix Chavany Marie Syndrome 22 0.047
189
PSY004 Psychotic Disorder 67 0.042
190
P NMN002 Niemann-Pick Disease 66 0.042
191
P NRC002 Narcolepsy 62 0.042
192
RBR001 Roberts Syndrome 61 0.042
193
P SLP006 Sleep Apnea 60 0.042
194
P EPD009 Epidermolysis Bullosa Dystrophica 56 0.042
195
P RTN016 Retinal Degeneration 53 0.042
196
c ALZ037 Alzheimer Disease-2 52 0.042
197
VSC002 Vascular Dementia 52 0.042
198
GST037 Gastroparesis 52 0.042
199
RST001 Restless Legs Syndrome 52 0.042
200
c VRL007 Viral Encephalitis 51 0.042
201
P GNG025 Gingival Fibromatosis 51 0.042
202
PRT058 Pure Autonomic Failure 50 0.042
203
c OPT055 Optic Atrophy Plus Syndrome 50 0.042
204
TXC002 Toxic Encephalopathy 50 0.042
205
NSD001 Nose Disease 49 0.042
206
ALC009 Alcoholic Liver Cirrhosis 48 0.042
207
LYM116 Lymph Node Disease 47 0.042
208
OLV001 Olivopontocerebellar Atrophy 47 0.042
209
P CRB019 Cerebral Amyloid Angiopathy 46 0.042
210
BNN003 Bone Inflammation Disease 45 0.042
211
NSY001 N Syndrome 44 0.042
212
DNT016 Dentatorubro-Pallidoluysian Atrophy 44 0.042
213
c CHR095 Chronic Progressive External Ophthalmoplegia 43 0.042
214
BSL009 Basal Ganglia Calcification 43 0.042
215
CNN011 Cenani-Lenz Syndactyly Syndrome 42 0.042
216
NRN008 Neuronal Intranuclear Inclusion Disease 41 0.042
217
TND004 Tendinopathy 40 0.042
218
BNS003 Binswanger's Disease 40 0.042
219
DRG002 Drug-Induced Hepatitis 39 0.042
220
SKN005 Skin Atrophy 39 0.042
221
ADL053 Adult Astrocytic Tumour 37 0.042
222
WRN005 Wrinkles 37 0.042
223
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 36 0.042
224
CNJ007 Conjunctivochalasis 35 0.042
225
ATY001 Atypical Depressive Disorder 34 0.042
226
LYS021 Loeys-Dietz Syndrome 3 33 0.042
227
WDS002 Woods Syndrome 32 0.042
228
P PRM016 Primary Optic Atrophy 31 0.042
229
SPR034 Superior Limbic Keratoconjunctivitis 30 0.042
230
PST086 Posterior Cortical Atrophy 30 0.042
231
P PRK073 Parkinson Disease Susceptibility 30 0.042
232
AKN002 Akinetic Mutism 30 0.042
233
c PRK052 Parkinson Disease 17 30 0.042
234
c SPN104 Spinocerebellar Ataxia 34 30 0.042
235
ORM002 Oromandibular Dystonia 30 0.042
236
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 29 0.042
237
VSL004 Visual Cortex Disease 28 0.042
238
HYP572 Hypoganglionosis 28 0.042
239
SBC014 Subclavian Steal Syndrome 28 0.042
240
SPS002 Spastic Entropion 27 0.042
241
RCM004 Recombinant 8 Syndrome 26 0.042
242
c ALZ014 Alzheimer Disease 16 23 0.042
243
c SPS203 Spastic Paraplegia 78, Autosomal Recessive 23 0.042
244
BRN097 Brainstem Auditory Evoked Responses 22 0.042
245
P GNR027 Generalized Peeling Skin Syndrome 22 0.042
246
ISN001 Isoniazid Toxicity 22 0.042
247
c DYS033 Dysautonomia Like Disorder 22 0.042
248
ARS002 Arsacs 21 0.042
249
c OPT024 Optic Atrophy 5 21 0.042
250
CLR063 Colorblindness, Deutan 20 0.042
251
CRB007 Cerebral Sarcoidosis 20 0.042
252
HM3001 Hemi 3 Syndrome 18 0.042
253
PRM153 Primary Progressive Apraxia of Speech 18 0.042
254
NVD002 Nevada Syndrome 16 0.042
255
OGL001 Ogilvie Syndrome 15 0.042
256
CDN003 Codeine Toxicity 15 0.042
257
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 14 0.042
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