Search results for "progressive supranuclear palsy - corticobasal syndrome"

The MalaCard for "progressive supranuclear palsy - corticobasal syndrome" has been retired.
Searching MalaCards for entries containing "progressive supranuclear palsy - corticobasal syndrome"

150 hits were found for 'progressive supranuclear palsy - corticobasal syndrome'

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 58 4.668
2
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 7 3.368
3
SPR100 Supranuclear Palsy, Progressive Atypical 28 3.064
4
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.312
5
CLS047 Classic Progressive Supranuclear Palsy Syndrome 15 1.549
6
BRN071 Brain Injury 52 0.207
7
P LYM118 Lymphoma 70 0.180
8
P EPL164 Epilepsy 66 0.180
9
P CRV039 Cervicitis 44 0.177
10
c CNT035 Central Nervous System Disease 59 0.161
11
P MYP004 Myopathy 67 0.160
12
GLB003 Globe Disease 35 0.154
13
c SPR048 Supranuclear Palsy, Progressive, 3 13 0.150
14
ANR040 Aneurysm 57 0.149
15
P ADN016 Adenocarcinoma 69 0.143
16
c MLT009 Multiple Cranial Nerve Palsy 31 0.141
17
P PNM007 Pneumonia 66 0.137
18
P CRB042 Cerebellar Ataxia 64 0.136
19
P MSC033 Muscle Disorders 52 0.134
20
PSD001 Pseudobulbar Palsy 34 0.128
21
DYS073 Dysphagia 49 0.124
22
EXF001 Exfoliation Syndrome 57 0.122
23
CSY001 C Syndrome 49 0.119
24
MSC004 Muscle Tissue Disease 36 0.117
25
P LRY019 Laryngitis 55 0.117
26
MTR014 Motor Neuron Disease 59 0.116
27
P PLN008 Peeling Skin Syndrome 47 0.115
28
BRT030 Birth Defects 43 0.114
29
P MNN013 Meningitis 65 0.114
30
ACR041 Acromelic Frontonasal Dysostosis 46 0.111
31
MTH009 Mouth Disease 63 0.109
32
PRD011 Proud Syndrome 42 0.106
33
PHY002 Physical Disorder 44 0.104
34
GLT021 Glutaricaciduria, Type I 48 0.103
35
INT042 Internuclear Ophthalmoplegia 36 0.099
36
ETH011 Ethylmalonic Encephalopathy 59 0.099
37
EYD002 Eye Disease 63 0.098
38
ATN005 Autonomic Dysfunction 45 0.095
39
HMP005 Hemiplegia 54 0.094
40
HRP004 Herpes Zoster 56 0.094
41
c PRK025 Parkinson Disease 10 42 0.094
42
KFR001 Kufor-Rakeb Syndrome 46 0.093
43
c PLN018 Peeling Skin Syndrome 2 35 0.092
44
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.091
45
PRP027 Peripheral Vascular Disease 69 0.091
46
c CHR095 Chronic Progressive External Ophthalmoplegia 45 0.091
47
P PRS038 Personality Disorder 61 0.090
48
PRG007 Progressive Bulbar Palsy 31 0.090
49
P PTS002 Ptosis 56 0.089
50
P BCL006 B-Cell Lymphomas 64 0.089
51
c PLN021 Peeling Skin Syndrome 3 31 0.088
52
HPT074 Hepatic Adenoma, Somatic 51 0.087
53
RST001 Restless Legs Syndrome 54 0.087
54
ART016 Aortic Aneurysm 67 0.086
55
SWL001 Swallowing Disorders 34 0.084
56
ATN002 Autonomic Nervous System Disease 47 0.083
57
P SLP006 Sleep Apnea 61 0.083
58
LPD008 Lipid Metabolism Disorder 58 0.082
59
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.082
60
HNM002 Hinman Syndrome 25 0.081
61
P GNR027 Generalized Peeling Skin Syndrome 22 0.081
62
VTM003 Vitamin Metabolic Disorder 33 0.081
63
PRT015 Partial Third-Nerve Palsy 27 0.080
64
P DYS021 Dysautonomia 47 0.080
65
BLD054 Blood Protein Disease 40 0.078
66
BNF002 Bone Fracture 47 0.077
67
c TRC078 Trichohepatoenteric Syndrome 2 31 0.077
68
SPC003 Specific Developmental Disorder 40 0.077
69
c PLN017 Peeling Skin Syndrome 1 33 0.076
70
P OST012 Osteoarthritis 82 0.076
71
ADT003 Auditory System Disease 51 0.073
72
TXC002 Toxic Encephalopathy 51 0.073
73
CNJ001 Conjugate Gaze Palsy 22 0.073
74
P HYP024 Hypoparathyroidism 52 0.072
75
P SYP003 Syphilis 53 0.071
76
c OPT055 Optic Atrophy Plus Syndrome 54 0.070
77
ABL002 Ablepharon-Macrostomia Syndrome 57 0.070
78
SXD001 Sex Differentiation Disease 40 0.070
79
P OST002 Osteoporosis 64 0.070
80
OBS003 Obsessive-Compulsive Personality Disorder 37 0.069
81
TTN003 Tetanus 61 0.069
82
ADP007 Adie Pupil 34 0.069
83
c PRK022 Parkinson Disease 12 24 0.068
84
CND002 Conduct Disorder 56 0.068
85
P BLP003 Blepharospasm 44 0.068
86
SBC014 Subclavian Steal Syndrome 29 0.067
87
PRR007 Perry Syndrome 57 0.067
88
c ESS001 Essential Tremor 61 0.065
89
ASP007 Aspiration Pneumonia 46 0.065
90
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.064
91
P PRM016 Primary Optic Atrophy 32 0.063
92
OCL003 Oculomotor Nerve Paralysis 27 0.062
93
PRM157 Primary Progressive Freezing Gait 12 0.062
94
SPS019 Spastic Paraparesis 34 0.061
95
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.061
96
EXT022 Exotropia 39 0.061
97
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.060
98
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.060
99
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.059
100
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.059
101
NSD001 Nose Disease 52 0.058
102
c NMN015 Niemann-Pick Disease, Type C1 64 0.058
103
c PRK059 Parkinson Disease 8 52 0.058
104
c PRK030 Parkinson Disease 4 39 0.058
105
SYN058 Synucleinopathy 39 0.058
106
TSY001 Tau Syndrome 12 0.057
107
PSY004 Psychotic Disorder 67 0.057
108
P MTC069 Mitochondrial Disorders 52 0.057
109
CLN006 Colonic Pseudo-Obstruction 34 0.056
110
FXC001 Foix Chavany Marie Syndrome 20 0.055
111
c SCN006 Secondary Syphilis 41 0.055
112
c BNG076 Benign Exophthalmos Syndrome 14 0.054
113
c GCH017 Gaucher Disease, Type Iii 45 0.054
114
DRG001 Drug Psychosis 40 0.054
115
VSC009 Vascular Skin Disease 22 0.053
116
c DYS033 Dysautonomia Like Disorder 19 0.052
117
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 13 0.052
118
MTC005 Mitochondrial Metabolism Disease 38 0.052
119
P CRB019 Cerebral Amyloid Angiopathy 58 0.052
120
VST004 Vestibular Disease 47 0.051
121
PNC056 Pineocytoma 40 0.051
122
P NRC002 Narcolepsy 62 0.050
123
BRN014 Bronchopneumonia 45 0.050
124
MSC077 Muscle Eye Brain Disease 56 0.049
125
CDS001 Cadasil 50 0.049
126
c OPT023 Optic Atrophy 2 27 0.048
127
P KRN004 Kernicterus 46 0.048
128
LYS021 Loeys-Dietz Syndrome 3 30 0.048
129
P NMN002 Niemann-Pick Disease 63 0.048
130
PRM153 Primary Progressive Apraxia of Speech 11 0.046
131
SML020 Small Patella Syndrome 36 0.046
132
OGL001 Ogilvie Syndrome 15 0.046
133
DNT016 Dentatorubro-Pallidoluysian Atrophy 48 0.045
134
SKN005 Skin Atrophy 43 0.044
135
RCM004 Recombinant 8 Syndrome 18 0.044
136
OCL010 Ocular Hypotension 42 0.043
137
BRN097 Brainstem Auditory Evoked Responses 23 0.043
138
WRN005 Wrinkles 37 0.042
139
c SPN294 Spinocerebellar Ataxia 1 55 0.042
140
c PRK020 Parkinson Disease 6, Early Onset 47 0.042
141
c ALZ014 Alzheimer Disease 16 23 0.041
142
ORM002 Oromandibular Dystonia 31 0.041
143
c OPT024 Optic Atrophy 5 20 0.041
144
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 41 0.040
145
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 28 0.040
146
THR010 Third Cranial Nerve Disease 28 0.040
147
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 21 0.039
148
c SPS072 Spastic Ataxia 1, Autosomal Dominant 26 0.039
149
c PRK052 Parkinson Disease 17 28 0.037
150
MNS002 Mini Stroke 19 0.037