Search results for "supranuclear palsy"

The MalaCard for "supranuclear palsy" has been retired.
Searching MalaCards for entries containing "supranuclear palsy"

230 hits were found for 'supranuclear palsy'

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 57 10.667
2
SPR100 Supranuclear Palsy, Progressive Atypical 27 6.815
3
SPR038 Supranuclear Ocular Palsy 20 3.846
4
c SPR049 Supranuclear Palsy, Progressive, 2 19 3.623
5
c SPR048 Supranuclear Palsy, Progressive, 3 11 3.566
6
CLS047 Classic Progressive Supranuclear Palsy Syndrome 16 3.466
7
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 8 3.400
8
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 10 2.494
9
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.437
10
c PRG046 Progressive Supranuclear Palsy, Mapt-Related 5 2.421
11
CRB037 Cerebral Palsy 54 0.673
12
CRB009 Cerebritis 36 0.593
13
P CRT033 Corticobasal Degeneration 44 0.450
14
P CRN035 Cranial Nerve Palsy 44 0.385
15
SPS057 Spasticity 41 0.354
16
MLT021 Multiple System Atrophy 71 0.322
17
DMN002 Dementia 62 0.296
18
MVM001 Movement Disease 45 0.286
19
P ENC018 Encephalopathy 59 0.274
20
TPT001 Tauopathy 51 0.262
21
CRN031 Cranial Nerve Disease 39 0.242
22
BRN071 Brain Injury 51 0.232
23
OCL011 Ocular Motility Disease 41 0.229
24
OPT006 Optic Nerve Disease 47 0.228
25
FST001 Foster-Kennedy Syndrome 31 0.228
26
KRN002 Kearns-Sayre Syndrome 60 0.226
27
MTR031 Motor Neuro-Ophthalmic Disorders 22 0.225
28
BSL008 Basal Ganglia Disease 40 0.225
29
NRN002 Neuronitis 40 0.207
30
GLB003 Globe Disease 34 0.202
31
ETH011 Ethylmalonic Encephalopathy 57 0.199
32
EYD002 Eye Disease 62 0.199
33
P NRV007 Nervous System Disease 71 0.182
34
P PRK057 Parkinson Disease, Late-Onset 72 0.174
35
P DYS154 Dystonia 62 0.168
36
APR001 Apraxia 50 0.168
37
ALN001 Aland Island Eye Disease 45 0.168
38
APH002 Aphasia 52 0.167
39
PSD001 Pseudobulbar Palsy 33 0.161
40
c MLT009 Multiple Cranial Nerve Palsy 29 0.161
41
PNM010 Pneumothorax, Primary Spontaneous 34 0.159
42
CRT078 Corticobasal Syndrome 36 0.153
43
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 0.143
44
P LTR001 Lateral Sclerosis 50 0.139
45
P ATX004 Ataxia 53 0.128
46
c CNT035 Central Nervous System Disease 60 0.127
47
P CRT072 Creutzfeldt-Jakob Disease 62 0.124
48
SPC005 Speech Disorder 41 0.122
49
DYS073 Dysphagia 51 0.122
50
P ALZ034 Alzheimer Disease 92 0.120
51
c PRK045 Parkinson Disease 5 43 0.120
52
P MYP004 Myopathy 67 0.119
53
PCK002 Pick Disease 66 0.118
54
P MSC033 Muscle Disorders 52 0.117
55
MTR014 Motor Neuron Disease 57 0.117
56
P CRB042 Cerebellar Ataxia 64 0.117
57
P TRM003 Tremor 54 0.115
58
c PRK031 Parkinson Disease 1 54 0.115
59
P CRV039 Cervicitis 45 0.114
60
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 25 0.113
61
P PNM007 Pneumonia 67 0.113
62
ALR002 Al-Raqad Syndrome 36 0.112
63
INT042 Internuclear Ophthalmoplegia 36 0.110
64
CRB033 Cerebral Degeneration 45 0.109
65
SPC010 Speech and Communication Disorders 42 0.108
66
MSC004 Muscle Tissue Disease 35 0.108
67
KFR001 Kufor-Rakeb Syndrome 44 0.104
68
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.104
69
P STR001 Striatonigral Degeneration 32 0.104
70
EYD001 Eye Degenerative Disease 31 0.104
71
CNJ001 Conjugate Gaze Palsy 20 0.103
72
ANR040 Aneurysm 56 0.101
73
P CRB088 Cerebral Atrophy 40 0.100
74
P EPL164 Epilepsy 60 0.098
75
P LRY019 Laryngitis 55 0.098
76
PRG007 Progressive Bulbar Palsy 28 0.098
77
P MNN013 Meningitis 66 0.096
78
HMP005 Hemiplegia 52 0.096
79
PRT015 Partial Third-Nerve Palsy 23 0.096
80
HRP004 Herpes Zoster 56 0.095
81
c PRK025 Parkinson Disease 10 41 0.095
82
GLT021 Glutaricaciduria, Type I 47 0.093
83
SWL001 Swallowing Disorders 33 0.093
84
MYC033 Myoclonus 41 0.093
85
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.092
86
P LYM118 Lymphoma 68 0.092
87
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 35 0.090
88
KHL003 Kohlschutter-Tonz Syndrome 35 0.090
89
P HYD006 Hydrocephalus 68 0.085
90
NWC001 Newcastle Disease 51 0.085
91
CHR158 Charles Bonnet Syndrome 24 0.085
92
RMS001 Rem Sleep Behavior Disorder 40 0.085
93
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.084
94
DSS008 Disease of Mental Health 48 0.082
95
PRD011 Proud Syndrome 42 0.082
96
HPT074 Hepatic Adenoma, Somatic 35 0.082
97
MTH009 Mouth Disease 63 0.081
98
BRT030 Birth Defects 44 0.081
99
ADR009 Adrenal Cortex Disease 40 0.080
100
BNF002 Bone Fracture 46 0.079
101
MVD001 Moved to 60 0.078
102
ACR041 Acromelic Frontonasal Dysostosis 45 0.076
103
NRL004 Neuroleptic Malignant Syndrome 48 0.075
104
P ENC004 Encephalitis 60 0.075
105
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.075
106
PRG033 Progressive Non-Fluent Aphasia 16 0.074
107
VTM003 Vitamin Metabolic Disorder 31 0.074
108
ASP007 Aspiration Pneumonia 46 0.073
109
LMB012 Limb Dystonia 22 0.073
110
MBS002 Moebius Syndrome 44 0.073
111
ATN002 Autonomic Nervous System Disease 46 0.073
112
P BLP003 Blepharospasm 43 0.071
113
EXT022 Exotropia 37 0.071
114
P PTS002 Ptosis 56 0.069
115
STR067 Stroke, Ischemic 74 0.067
116
c PRK024 Parkinson Disease, Juvenile, Type 2 49 0.067
117
P PRS038 Personality Disorder 60 0.067
118
OCL003 Oculomotor Nerve Paralysis 26 0.067
119
TTN003 Tetanus 62 0.067
120
P SYP003 Syphilis 51 0.067
121
PHY002 Physical Disorder 43 0.065
122
SPC003 Specific Developmental Disorder 39 0.065
123
c NMN015 Niemann-Pick Disease, Type C1 63 0.065
124
c ESS001 Essential Tremor 58 0.064
125
PRR007 Perry Syndrome 58 0.064
126
EXF001 Exfoliation Syndrome 56 0.064
127
P PLN008 Peeling Skin Syndrome 45 0.064
128
NRM002 Normal Pressure Hydrocephalus 47 0.064
129
ATN005 Autonomic Dysfunction 44 0.064
130
P HYP024 Hypoparathyroidism 52 0.063
131
c TRC078 Trichohepatoenteric Syndrome 2 30 0.063
132
P ADN016 Adenocarcinoma 69 0.063
133
NRS003 Neurosyphilis 41 0.063
134
ADT003 Auditory System Disease 49 0.060
135
c SCN006 Secondary Syphilis 41 0.060
136
CLN006 Colonic Pseudo-Obstruction 36 0.060
137
P DMN033 Dementia, Frontotemporal 63 0.060
138
c OPT055 Optic Atrophy Plus Syndrome 55 0.060
139
c GCH017 Gaucher Disease, Type Iii 44 0.060
140
LYS021 Loeys-Dietz Syndrome 3 30 0.060
141
c NMN014 Niemann-Pick Disease, Type C2 39 0.060
142
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 28 0.060
143
SML020 Small Patella Syndrome 36 0.060
144
c PRK030 Parkinson Disease 4 38 0.060
145
CLR063 Colorblindness, Deutan 28 0.060
146
TXC002 Toxic Encephalopathy 52 0.060
147
SMN008 Semantic Dementia 43 0.060
148
c PRK022 Parkinson Disease 12 22 0.060
149
ATY001 Atypical Depressive Disorder 34 0.060
150
P DYS021 Dysautonomia 47 0.060
151
SYN058 Synucleinopathy 38 0.060
152
P PRM016 Primary Optic Atrophy 29 0.060
153
TSY001 Tau Syndrome 11 0.060
154
c FML118 Familial Creutzfeldt-Jakob Disease 23 0.060
155
PRM157 Primary Progressive Freezing Gait 11 0.060
156
P BCL006 B-Cell Lymphomas 64 0.058
157
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 38 0.055
158
ABL002 Ablepharon-Macrostomia Syndrome 51 0.055
159
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.055
160
P KRN004 Kernicterus 46 0.055
161
ART016 Aortic Aneurysm 67 0.051
162
ACD009 Acid-Labile Subunit, Deficiency of 37 0.051
163
BRN014 Bronchopneumonia 45 0.051
164
FXC001 Foix Chavany Marie Syndrome 22 0.051
165
MTC005 Mitochondrial Metabolism Disease 37 0.051
166
P OST002 Osteoporosis 63 0.048
167
P GCH001 Gaucher's Disease 63 0.048
168
CSY001 C Syndrome 49 0.048
169
ADL002 Adult Syndrome 53 0.048
170
c PLN018 Peeling Skin Syndrome 2 36 0.048
171
MSC077 Muscle Eye Brain Disease 54 0.048
172
c PLN021 Peeling Skin Syndrome 3 30 0.048
173
CND002 Conduct Disorder 54 0.048
174
c PRK026 Parkinson Disease 11 30 0.048
175
PNC056 Pineocytoma 29 0.048
176
DRG001 Drug Psychosis 39 0.048
177
SXD001 Sex Differentiation Disease 39 0.048
178
VSL004 Visual Cortex Disease 28 0.048
179
DPB001 Deep Brain Stimulation for Parkinson's Disease 23 0.048
180
PSY004 Psychotic Disorder 62 0.042
181
P NRC002 Narcolepsy 62 0.042
182
c SPN294 Spinocerebellar Ataxia 1 54 0.042
183
DNT016 Dentatorubro-Pallidoluysian Atrophy 49 0.042
184
P OST012 Osteoarthritis 81 0.042
185
P NMN002 Niemann-Pick Disease 63 0.042
186
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.042
187
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.042
188
P CRB019 Cerebral Amyloid Angiopathy 56 0.042
189
c PRK020 Parkinson Disease 6, Early Onset 46 0.042
190
PRP027 Peripheral Vascular Disease 69 0.042
191
RST001 Restless Legs Syndrome 51 0.042
192
c PRK059 Parkinson Disease 8 51 0.042
193
P MTC069 Mitochondrial Disorders 51 0.042
194
MDD011 Mood Disorder 60 0.042
195
c PRK071 Parkinson Disease 14, Autosomal Recessive 23 0.042
196
LPD008 Lipid Metabolism Disorder 42 0.042
197
c PRK052 Parkinson Disease 17 27 0.042
198
c SPS072 Spastic Ataxia 1, Autosomal Dominant 25 0.042
199
c PRK065 Parkinson Disease 20, Early-Onset 23 0.042
200
NSD001 Nose Disease 51 0.042
201
CDS001 Cadasil 50 0.042
202
BSL009 Basal Ganglia Calcification 41 0.042
203
NSY001 N Syndrome 42 0.042
204
P SLP006 Sleep Apnea 60 0.042
205
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 28 0.042
206
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 0.042
207
c OPT023 Optic Atrophy 2 25 0.042
208
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 21 0.042
209
OBS003 Obsessive-Compulsive Personality Disorder 36 0.042
210
OCL010 Ocular Hypotension 42 0.042
211
ARS002 Arsacs 22 0.042
212
THR010 Third Cranial Nerve Disease 27 0.042
213
SBC014 Subclavian Steal Syndrome 30 0.042
214
IDM001 Ideomotor Apraxia 34 0.042
215
SKN005 Skin Atrophy 42 0.042
216
OGL001 Ogilvie Syndrome 17 0.042
217
VSC009 Vascular Skin Disease 21 0.042
218
ORM002 Oromandibular Dystonia 29 0.042
219
P GNR027 Generalized Peeling Skin Syndrome 21 0.042
220
c OPT024 Optic Atrophy 5 18 0.042
221
BLD054 Blood Protein Disease 38 0.042
222
RCM004 Recombinant 8 Syndrome 17 0.042
223
c ALZ014 Alzheimer Disease 16 17 0.042
224
SPS019 Spastic Paraparesis 34 0.042
225
MNS002 Mini Stroke 18 0.042
226
CRB007 Cerebral Sarcoidosis 19 0.042
227
PRM153 Primary Progressive Apraxia of Speech 9 0.042
228
c DYS033 Dysautonomia Like Disorder 18 0.042
229
BRN097 Brainstem Auditory Evoked Responses 21 0.042
230
WRN005 Wrinkles 35 0.042