Search results for supranuclear palsy

243 hits were found for supranuclear palsy

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 56 10.695
2
SPR100 Supranuclear Palsy, Progressive Atypical 28 6.823
3
SPR038 Supranuclear Ocular Palsy 15 3.864
4
c SPR049 Supranuclear Palsy, Progressive, 2 18 3.653
5
c SPR048 Supranuclear Palsy, Progressive, 3 13 3.582
6
CLS047 Classic Progressive Supranuclear Palsy Syndrome 15 3.444
7
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 7 3.408
8
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 9 2.498
9
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.443
10
c PRG046 Progressive Supranuclear Palsy, Mapt-Related 5 2.427
11
CRB037 Cerebral Palsy 66 0.678
12
CRB009 Cerebritis 39 0.591
13
P CRT033 Corticobasal Degeneration 47 0.444
14
P CRN035 Cranial Nerve Palsy 46 0.385
15
SPS057 Spasticity 42 0.353
16
MLT021 Multiple System Atrophy 70 0.324
17
MVM001 Movement Disease 49 0.286
18
DMN002 Dementia 65 0.284
19
CRN031 Cranial Nerve Disease 40 0.248
20
BRN071 Brain Injury 52 0.238
21
OPT006 Optic Nerve Disease 52 0.238
22
FST001 Foster-Kennedy Syndrome 31 0.237
23
OCL011 Ocular Motility Disease 37 0.235
24
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.232
25
KRN002 Kearns-Sayre Syndrome 61 0.230
26
BSL008 Basal Ganglia Disease 40 0.229
27
NRN002 Neuronitis 41 0.192
28
P PRK057 Parkinson Disease, Late-Onset 70 0.186
29
P ENC018 Encephalopathy 59 0.185
30
P DYS154 Dystonia 65 0.165
31
c MLT009 Multiple Cranial Nerve Palsy 33 0.165
32
APR001 Apraxia 51 0.158
33
PSD001 Pseudobulbar Palsy 33 0.156
34
c CNT035 Central Nervous System Disease 60 0.155
35
APH002 Aphasia 54 0.151
36
P NRV007 Nervous System Disease 71 0.143
37
P ATX004 Ataxia 53 0.141
38
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.140
39
P LTR001 Lateral Sclerosis 53 0.132
40
GLB003 Globe Disease 32 0.129
41
P CRB042 Cerebellar Ataxia 63 0.128
42
c PRK031 Parkinson Disease 1 51 0.127
43
c PRK045 Parkinson Disease 5 40 0.125
44
PCK002 Pick Disease 68 0.123
45
P CRT072 Creutzfeldt-Jakob Disease 61 0.122
46
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 25 0.122
47
SPC005 Speech Disorder 41 0.119
48
P ALZ034 Alzheimer Disease 92 0.118
49
P MYP004 Myopathy 67 0.116
50
P MSC033 Muscle Disorders 52 0.116
51
DYS073 Dysphagia 48 0.115
52
PNM010 Pneumothorax, Primary Spontaneous 33 0.111
53
INT042 Internuclear Ophthalmoplegia 37 0.108
54
CRB033 Cerebral Degeneration 44 0.107
55
P CRV039 Cervicitis 45 0.107
56
SPN369 Spinal Disease 39 0.107
57
SPC010 Speech and Communication Disorders 41 0.107
58
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.106
59
MTR014 Motor Neuron Disease 58 0.105
60
KFR001 Kufor-Rakeb Syndrome 44 0.103
61
c PRK025 Parkinson Disease 10 38 0.102
62
EYD001 Eye Degenerative Disease 30 0.102
63
P STR001 Striatonigral Degeneration 28 0.102
64
P TRM003 Tremor 54 0.101
65
P CRB088 Cerebral Atrophy 42 0.098
66
P PNM007 Pneumonia 68 0.098
67
PRT015 Partial Third-Nerve Palsy 26 0.097
68
HMP005 Hemiplegia 51 0.097
69
PRG007 Progressive Bulbar Palsy 30 0.097
70
P LRY019 Laryngitis 54 0.096
71
ANR040 Aneurysm 57 0.096
72
MSC004 Muscle Tissue Disease 34 0.096
73
P MNN013 Meningitis 67 0.094
74
GLT021 Glutaricaciduria, Type I 46 0.093
75
SWL001 Swallowing Disorders 33 0.092
76
P EPL164 Epilepsy 66 0.090
77
CNJ001 Conjugate Gaze Palsy 29 0.090
78
HRP004 Herpes Zoster 56 0.090
79
P PRS038 Personality Disorder 62 0.089
80
P LYM118 Lymphoma 69 0.088
81
ALR002 Al-Raqad Syndrome 36 0.087
82
MYC033 Myoclonus 42 0.086
83
NWC001 Newcastle Disease 54 0.084
84
RMS001 Rem Sleep Behavior Disorder 41 0.084
85
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.082
86
MTH009 Mouth Disease 61 0.081
87
BRT030 Birth Defects 43 0.081
88
PRD011 Proud Syndrome 42 0.081
89
P HYD006 Hydrocephalus 66 0.078
90
ADR009 Adrenal Cortex Disease 39 0.078
91
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.078
92
ACR041 Acromelic Frontonasal Dysostosis 45 0.078
93
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.078
94
BNF002 Bone Fracture 50 0.077
95
EXF001 Exfoliation Syndrome 57 0.076
96
ATN005 Autonomic Dysfunction 49 0.076
97
P PLN008 Peeling Skin Syndrome 45 0.076
98
P ENC004 Encephalitis 63 0.074
99
OCL003 Oculomotor Nerve Paralysis 27 0.074
100
P DMN033 Dementia, Frontotemporal 62 0.072
101
SMN008 Semantic Dementia 44 0.072
102
OBS003 Obsessive-Compulsive Personality Disorder 36 0.072
103
VTM003 Vitamin Metabolic Disorder 30 0.072
104
c PRK022 Parkinson Disease 12 21 0.072
105
P PTS002 Ptosis 51 0.072
106
MBS002 Moebius Syndrome 47 0.072
107
PHY002 Physical Disorder 43 0.072
108
NRL004 Neuroleptic Malignant Syndrome 41 0.072
109
EXT022 Exotropia 39 0.070
110
ASP007 Aspiration Pneumonia 47 0.069
111
P BLP003 Blepharospasm 43 0.068
112
AND005 Androgen Insensitivity Syndrome, Mild 16 0.068
113
EYD002 Eye Disease 61 0.066
114
TTN003 Tetanus 61 0.064
115
SPC003 Specific Developmental Disorder 38 0.064
116
c NMN015 Niemann-Pick Disease, Type C1 63 0.063
117
c ESS001 Essential Tremor 59 0.063
118
ETH011 Ethylmalonic Encephalopathy 56 0.063
119
PRR007 Perry Syndrome 55 0.063
120
DSS008 Disease of Mental Health 52 0.063
121
NRM002 Normal Pressure Hydrocephalus 50 0.063
122
CSY001 C Syndrome 50 0.063
123
c PLN018 Peeling Skin Syndrome 2 40 0.063
124
c PLN021 Peeling Skin Syndrome 3 29 0.063
125
c TRC078 Trichohepatoenteric Syndrome 2 29 0.062
126
HPT074 Hepatic Adenoma, Somatic 50 0.059
127
ATN002 Autonomic Nervous System Disease 48 0.059
128
NRS003 Neurosyphilis 41 0.059
129
ADT003 Auditory System Disease 40 0.059
130
c OPT055 Optic Atrophy Plus Syndrome 52 0.059
131
TXC002 Toxic Encephalopathy 51 0.059
132
c PRK059 Parkinson Disease 8 48 0.059
133
c GCH017 Gaucher Disease, Type Iii 46 0.059
134
P DYS021 Dysautonomia 44 0.059
135
SYN058 Synucleinopathy 38 0.059
136
c PRK030 Parkinson Disease 4 38 0.059
137
c NMN014 Niemann-Pick Disease, Type C2 36 0.059
138
ATY001 Atypical Depressive Disorder 32 0.059
139
P PRM016 Primary Optic Atrophy 29 0.059
140
c FML118 Familial Creutzfeldt-Jakob Disease 28 0.059
141
PRG033 Progressive Non-Fluent Aphasia 27 0.059
142
CHR158 Charles Bonnet Syndrome 22 0.059
143
P GNR027 Generalized Peeling Skin Syndrome 19 0.059
144
PRM157 Primary Progressive Freezing Gait 13 0.059
145
TSY001 Tau Syndrome 10 0.059
146
P ADN016 Adenocarcinoma 69 0.057
147
P BCL006 B-Cell Lymphomas 65 0.057
148
P SYP003 Syphilis 53 0.057
149
STR067 Stroke, Ischemic 75 0.054
150
P KRN004 Kernicterus 46 0.054
151
VST004 Vestibular Disease 44 0.054
152
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.054
153
HNM002 Hinman Syndrome 25 0.054
154
P OST012 Osteoarthritis 83 0.051
155
ART016 Aortic Aneurysm 69 0.051
156
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
157
MSC077 Muscle Eye Brain Disease 57 0.051
158
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.051
159
P HYP024 Hypoparathyroidism 53 0.051
160
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.051
161
c SCN006 Secondary Syphilis 41 0.051
162
PNC056 Pineocytoma 39 0.051
163
SXD001 Sex Differentiation Disease 38 0.051
164
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.051
165
CLN006 Colonic Pseudo-Obstruction 31 0.051
166
THR010 Third Cranial Nerve Disease 26 0.051
167
c BNG076 Benign Exophthalmos Syndrome 15 0.051
168
PRP027 Peripheral Vascular Disease 68 0.047
169
P OST002 Osteoporosis 64 0.047
170
P GCH001 Gaucher's Disease 62 0.047
171
P SLP006 Sleep Apnea 61 0.047
172
c VRL007 Viral Encephalitis 54 0.047
173
CND002 Conduct Disorder 54 0.047
174
ADL002 Adult Syndrome 52 0.047
175
NSD001 Nose Disease 48 0.047
176
BLD054 Blood Protein Disease 37 0.047
177
ADP007 Adie Pupil 34 0.047
178
c PLN017 Peeling Skin Syndrome 1 34 0.047
179
c PRK026 Parkinson Disease 11 29 0.047
180
VSL004 Visual Cortex Disease 28 0.047
181
FXC001 Foix Chavany Marie Syndrome 21 0.047
182
PSY004 Psychotic Disorder 67 0.042
183
P NMN002 Niemann-Pick Disease 65 0.042
184
P NRC002 Narcolepsy 62 0.042
185
P CCK001 Cockayne Syndrome 61 0.042
186
MDD011 Mood Disorder 61 0.042
187
RBR001 Roberts Syndrome 60 0.042
188
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.042
189
P XRD010 Xeroderma Pigmentosum, Variant Type 58 0.042
190
LPD008 Lipid Metabolism Disorder 58 0.042
191
P CRB019 Cerebral Amyloid Angiopathy 58 0.042
192
WST001 West Syndrome 57 0.042
193
c SPN294 Spinocerebellar Ataxia 1 55 0.042
194
P CDS001 Cadasil 55 0.042
195
RST001 Restless Legs Syndrome 54 0.042
196
P MTC069 Mitochondrial Disorders 53 0.042
197
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.042
198
c XRD019 Xeroderma Pigmentosum, Group C 52 0.042
199
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 49 0.042
200
DNT016 Dentatorubro-Pallidoluysian Atrophy 47 0.042
201
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 47 0.042
202
c PRK020 Parkinson Disease 6, Early Onset 46 0.042
203
BRN014 Bronchopneumonia 45 0.042
204
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.042
205
BSL009 Basal Ganglia Calcification 43 0.042
206
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.042
207
SPS019 Spastic Paraparesis 41 0.042
208
SKN005 Skin Atrophy 40 0.042
209
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.042
210
OCL010 Ocular Hypotension 38 0.042
211
DRG001 Drug Psychosis 38 0.042
212
WRN005 Wrinkles 37 0.042
213
NSY001 N Syndrome 36 0.042
214
IDM001 Ideomotor Apraxia 36 0.042
215
SML020 Small Patella Syndrome 36 0.042
216
MTC005 Mitochondrial Metabolism Disease 36 0.042
217
P XRD027 Xeroderma Pigmentosum Group E 35 0.042
218
ORM002 Oromandibular Dystonia 31 0.042
219
CLR063 Colorblindness, Deutan 31 0.042
220
LYS021 Loeys-Dietz Syndrome 3 30 0.042
221
c PRK052 Parkinson Disease 17 29 0.042
222
XRD017 Xeroderma Pigmentosum, Group E, Ddb-Negative Subtype 28 0.042
223
SBC014 Subclavian Steal Syndrome 28 0.042
224
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 28 0.042
225
c PRK070 Parkinson Disease 21 27 0.042
226
WDS002 Woods Syndrome 27 0.042
227
c SPS072 Spastic Ataxia 1, Autosomal Dominant 27 0.042
228
c ALZ014 Alzheimer Disease 16 27 0.042
229
c PRK065 Parkinson Disease 20, Early-Onset 25 0.042
230
c OPT023 Optic Atrophy 2 25 0.042
231
c PRK071 Parkinson Disease 14, Autosomal Recessive 22 0.042
232
BRN097 Brainstem Auditory Evoked Responses 22 0.042
233
RCM004 Recombinant 8 Syndrome 22 0.042
234
ARS002 Arsacs 21 0.042
235
MNS002 Mini Stroke 19 0.042
236
VSC009 Vascular Skin Disease 19 0.042
237
CRB007 Cerebral Sarcoidosis 18 0.042
238
c OPT024 Optic Atrophy 5 17 0.042
239
c DYS033 Dysautonomia Like Disorder 16 0.042
240
OGL001 Ogilvie Syndrome 15 0.042
241
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 14 0.042
242
NVD002 Nevada Syndrome 14 0.042
243
PRM153 Primary Progressive Apraxia of Speech 11 0.042
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