Search results for "supranuclear palsy"

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

231 hits were found for 'supranuclear palsy'

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 58 10.682
2
SPR100 Supranuclear Palsy, Progressive Atypical 28 6.820
3
SPR038 Supranuclear Ocular Palsy 20 3.862
4
c SPR049 Supranuclear Palsy, Progressive, 2 20 3.639
5
c SPR048 Supranuclear Palsy, Progressive, 3 13 3.583
6
CLS047 Classic Progressive Supranuclear Palsy Syndrome 15 3.443
7
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 7 3.407
8
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 9 2.499
9
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.442
10
c PRG046 Progressive Supranuclear Palsy, Mapt-Related 5 2.426
11
CRB037 Cerebral Palsy 54 0.683
12
CRB009 Cerebritis 38 0.601
13
P CRT033 Corticobasal Degeneration 46 0.453
14
P CRN035 Cranial Nerve Palsy 43 0.387
15
SPS057 Spasticity 42 0.359
16
MLT021 Multiple System Atrophy 71 0.324
17
DMN002 Dementia 64 0.289
18
MVM001 Movement Disease 54 0.288
19
CRN031 Cranial Nerve Disease 40 0.245
20
BRN071 Brain Injury 52 0.237
21
P ENC018 Encephalopathy 59 0.234
22
OPT006 Optic Nerve Disease 51 0.233
23
FST001 Foster-Kennedy Syndrome 34 0.233
24
KRN002 Kearns-Sayre Syndrome 59 0.230
25
BSL008 Basal Ganglia Disease 43 0.228
26
OCL011 Ocular Motility Disease 38 0.228
27
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.228
28
NRN002 Neuronitis 42 0.196
29
P PRK057 Parkinson Disease, Late-Onset 72 0.184
30
c MLT009 Multiple Cranial Nerve Palsy 31 0.167
31
P DYS154 Dystonia 64 0.166
32
APR001 Apraxia 48 0.162
33
c CNT035 Central Nervous System Disease 59 0.160
34
PSD001 Pseudobulbar Palsy 34 0.159
35
APH002 Aphasia 53 0.154
36
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.143
37
P NRV007 Nervous System Disease 71 0.142
38
P ATX004 Ataxia 53 0.133
39
P LTR001 Lateral Sclerosis 52 0.133
40
GLB003 Globe Disease 35 0.131
41
c PRK031 Parkinson Disease 1 55 0.129
42
c PRK045 Parkinson Disease 5 44 0.127
43
P CRT072 Creutzfeldt-Jakob Disease 63 0.124
44
P CRB042 Cerebellar Ataxia 64 0.122
45
SPC005 Speech Disorder 43 0.121
46
P ALZ034 Alzheimer Disease 93 0.120
47
DYS073 Dysphagia 49 0.118
48
P MYP004 Myopathy 67 0.116
49
P MSC033 Muscle Disorders 52 0.115
50
GZP002 Gaze Palsy, Horizontal, with Progressive Scoliosis 24 0.113
51
PNM010 Pneumothorax, Primary Spontaneous 33 0.112
52
PCK002 Pick Disease 67 0.111
53
INT042 Internuclear Ophthalmoplegia 36 0.110
54
P CRV039 Cervicitis 44 0.109
55
CRB033 Cerebral Degeneration 46 0.109
56
SPC010 Speech and Communication Disorders 46 0.108
57
SPN369 Spinal Disease 41 0.107
58
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.107
59
MTR014 Motor Neuron Disease 59 0.106
60
KFR001 Kufor-Rakeb Syndrome 46 0.104
61
c PRK025 Parkinson Disease 10 42 0.104
62
EYD001 Eye Degenerative Disease 31 0.104
63
P STR001 Striatonigral Degeneration 27 0.104
64
P TRM003 Tremor 54 0.102
65
P CRB088 Cerebral Atrophy 42 0.100
66
P PNM007 Pneumonia 66 0.098
67
P LRY019 Laryngitis 55 0.098
68
PRT015 Partial Third-Nerve Palsy 27 0.098
69
ANR040 Aneurysm 57 0.098
70
HMP005 Hemiplegia 54 0.097
71
MSC004 Muscle Tissue Disease 36 0.095
72
P MNN013 Meningitis 65 0.093
73
PRG007 Progressive Bulbar Palsy 31 0.093
74
GLT021 Glutaricaciduria, Type I 48 0.093
75
SWL001 Swallowing Disorders 34 0.093
76
CNJ001 Conjugate Gaze Palsy 22 0.092
77
HRP004 Herpes Zoster 56 0.092
78
P PRS038 Personality Disorder 61 0.090
79
P EPL164 Epilepsy 66 0.090
80
P LYM118 Lymphoma 70 0.088
81
PHY002 Physical Disorder 44 0.087
82
MYC033 Myoclonus 41 0.087
83
ALR002 Al-Raqad Syndrome 36 0.087
84
NWC001 Newcastle Disease 54 0.085
85
RMS001 Rem Sleep Behavior Disorder 40 0.085
86
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.084
87
BRT030 Birth Defects 43 0.082
88
PRD011 Proud Syndrome 42 0.082
89
MTH009 Mouth Disease 63 0.081
90
ACR041 Acromelic Frontonasal Dysostosis 46 0.081
91
ADR009 Adrenal Cortex Disease 41 0.080
92
BNF002 Bone Fracture 47 0.078
93
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.078
94
P HYD006 Hydrocephalus 67 0.077
95
EXF001 Exfoliation Syndrome 57 0.077
96
P PLN008 Peeling Skin Syndrome 47 0.077
97
ATN005 Autonomic Dysfunction 45 0.077
98
P DMN033 Dementia, Frontotemporal 63 0.073
99
OBS003 Obsessive-Compulsive Personality Disorder 37 0.073
100
VTM003 Vitamin Metabolic Disorder 33 0.073
101
c PRK022 Parkinson Disease 12 24 0.073
102
P ENC004 Encephalitis 61 0.073
103
NRL004 Neuroleptic Malignant Syndrome 45 0.073
104
ASP007 Aspiration Pneumonia 46 0.070
105
OCL003 Oculomotor Nerve Paralysis 27 0.070
106
P PTS002 Ptosis 56 0.069
107
P BLP003 Blepharospasm 44 0.069
108
MBS002 Moebius Syndrome 44 0.069
109
EXT022 Exotropia 39 0.069
110
SPC003 Specific Developmental Disorder 40 0.065
111
c TRC078 Trichohepatoenteric Syndrome 2 31 0.065
112
AND005 Androgen Insensitivity Syndrome, Mild 16 0.065
113
c NMN015 Niemann-Pick Disease, Type C1 64 0.064
114
c ESS001 Essential Tremor 61 0.064
115
ETH011 Ethylmalonic Encephalopathy 59 0.064
116
PRR007 Perry Syndrome 57 0.064
117
DSS008 Disease of Mental Health 55 0.064
118
NRM002 Normal Pressure Hydrocephalus 50 0.064
119
CSY001 C Syndrome 49 0.064
120
KHL003 Kohlschutter-Tonz Syndrome 37 0.064
121
c PLN018 Peeling Skin Syndrome 2 35 0.064
122
c PLN021 Peeling Skin Syndrome 3 31 0.064
123
TTN003 Tetanus 61 0.063
124
STR067 Stroke, Ischemic 77 0.060
125
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.060
126
P SYP003 Syphilis 53 0.060
127
ADT003 Auditory System Disease 51 0.060
128
ATN002 Autonomic Nervous System Disease 47 0.060
129
NRS003 Neurosyphilis 41 0.060
130
EYD002 Eye Disease 63 0.060
131
c OPT055 Optic Atrophy Plus Syndrome 54 0.060
132
c PRK059 Parkinson Disease 8 52 0.060
133
TXC002 Toxic Encephalopathy 51 0.060
134
P DYS021 Dysautonomia 47 0.060
135
c GCH017 Gaucher Disease, Type Iii 45 0.060
136
SMN008 Semantic Dementia 44 0.060
137
c NMN014 Niemann-Pick Disease, Type C2 40 0.060
138
c PRK030 Parkinson Disease 4 39 0.060
139
SYN058 Synucleinopathy 39 0.060
140
ATY001 Atypical Depressive Disorder 35 0.060
141
P PRM016 Primary Optic Atrophy 32 0.060
142
c FML118 Familial Creutzfeldt-Jakob Disease 27 0.060
143
CHR158 Charles Bonnet Syndrome 23 0.060
144
P GNR027 Generalized Peeling Skin Syndrome 22 0.060
145
PRG033 Progressive Non-Fluent Aphasia 19 0.060
146
PRM157 Primary Progressive Freezing Gait 12 0.060
147
TSY001 Tau Syndrome 12 0.060
148
P ADN016 Adenocarcinoma 69 0.058
149
P BCL006 B-Cell Lymphomas 64 0.058
150
P HYP024 Hypoparathyroidism 52 0.058
151
HPT074 Hepatic Adenoma, Somatic 51 0.058
152
ALN001 Aland Island Eye Disease 45 0.058
153
c SCN006 Secondary Syphilis 41 0.055
154
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.055
155
CLN006 Colonic Pseudo-Obstruction 34 0.055
156
ART016 Aortic Aneurysm 67 0.051
157
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
158
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.051
159
VST004 Vestibular Disease 47 0.051
160
P KRN004 Kernicterus 46 0.051
161
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.051
162
SXD001 Sex Differentiation Disease 40 0.051
163
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.051
164
HNM002 Hinman Syndrome 25 0.051
165
P OST002 Osteoporosis 64 0.048
166
CND002 Conduct Disorder 56 0.048
167
MSC077 Muscle Eye Brain Disease 56 0.048
168
BRN014 Bronchopneumonia 45 0.048
169
PNC056 Pineocytoma 40 0.048
170
MTC005 Mitochondrial Metabolism Disease 38 0.048
171
ADP007 Adie Pupil 34 0.048
172
c PLN017 Peeling Skin Syndrome 1 33 0.048
173
c PRK026 Parkinson Disease 11 30 0.048
174
VSL004 Visual Cortex Disease 29 0.048
175
FXC001 Foix Chavany Marie Syndrome 20 0.048
176
c BNG076 Benign Exophthalmos Syndrome 14 0.048
177
P OST012 Osteoarthritis 82 0.042
178
PRP027 Peripheral Vascular Disease 69 0.042
179
PSY004 Psychotic Disorder 67 0.042
180
P NMN002 Niemann-Pick Disease 63 0.042
181
P NRC002 Narcolepsy 62 0.042
182
MDD011 Mood Disorder 61 0.042
183
P SLP006 Sleep Apnea 61 0.042
184
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.042
185
LPD008 Lipid Metabolism Disorder 58 0.042
186
P CRB019 Cerebral Amyloid Angiopathy 58 0.042
187
c SPN294 Spinocerebellar Ataxia 1 55 0.042
188
RST001 Restless Legs Syndrome 54 0.042
189
ADL002 Adult Syndrome 53 0.042
190
P MTC069 Mitochondrial Disorders 52 0.042
191
NSD001 Nose Disease 52 0.042
192
CDS001 Cadasil 50 0.042
193
DNT016 Dentatorubro-Pallidoluysian Atrophy 48 0.042
194
c PRK020 Parkinson Disease 6, Early Onset 47 0.042
195
c CHR095 Chronic Progressive External Ophthalmoplegia 45 0.042
196
SKN005 Skin Atrophy 43 0.042
197
BSL009 Basal Ganglia Calcification 43 0.042
198
OCL010 Ocular Hypotension 42 0.042
199
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.042
200
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 41 0.042
201
DRG001 Drug Psychosis 40 0.042
202
BLD054 Blood Protein Disease 40 0.042
203
NSY001 N Syndrome 39 0.042
204
WRN005 Wrinkles 37 0.042
205
IDM001 Ideomotor Apraxia 36 0.042
206
SML020 Small Patella Syndrome 36 0.042
207
CLR063 Colorblindness, Deutan 34 0.042
208
SPS019 Spastic Paraparesis 34 0.042
209
ORM002 Oromandibular Dystonia 31 0.042
210
LYS021 Loeys-Dietz Syndrome 3 30 0.042
211
SBC014 Subclavian Steal Syndrome 29 0.042
212
c PRK052 Parkinson Disease 17 28 0.042
213
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 28 0.042
214
THR010 Third Cranial Nerve Disease 28 0.042
215
c OPT023 Optic Atrophy 2 27 0.042
216
c SPS072 Spastic Ataxia 1, Autosomal Dominant 26 0.042
217
c PRK065 Parkinson Disease 20, Early-Onset 23 0.042
218
c ALZ014 Alzheimer Disease 16 23 0.042
219
BRN097 Brainstem Auditory Evoked Responses 23 0.042
220
VSC009 Vascular Skin Disease 22 0.042
221
ARS002 Arsacs 22 0.042
222
c PRK071 Parkinson Disease 14, Autosomal Recessive 22 0.042
223
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 21 0.042
224
c OPT024 Optic Atrophy 5 20 0.042
225
CRB007 Cerebral Sarcoidosis 19 0.042
226
c DYS033 Dysautonomia Like Disorder 19 0.042
227
MNS002 Mini Stroke 19 0.042
228
RCM004 Recombinant 8 Syndrome 18 0.042
229
OGL001 Ogilvie Syndrome 15 0.042
230
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 13 0.042
231
PRM153 Primary Progressive Apraxia of Speech 11 0.042