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"

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

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 57 4.668
2
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 8 3.369
3
SPR100 Supranuclear Palsy, Progressive Atypical 27 3.063
4
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.312
5
CLS047 Classic Progressive Supranuclear Palsy Syndrome 16 1.549
6
SPS057 Spasticity 41 0.322
7
BRN071 Brain Injury 51 0.205
8
P EPL164 Epilepsy 60 0.189
9
P LYM118 Lymphoma 68 0.184
10
P CRV039 Cervicitis 45 0.183
11
P MYP004 Myopathy 67 0.167
12
ANR040 Aneurysm 56 0.153
13
P PNM007 Pneumonia 67 0.152
14
P ADN016 Adenocarcinoma 69 0.150
15
c SPR048 Supranuclear Palsy, Progressive, 3 11 0.146
16
P MSC033 Muscle Disorders 52 0.136
17
c MLT009 Multiple Cranial Nerve Palsy 29 0.136
18
P CRB042 Cerebellar Ataxia 64 0.134
19
PSD001 Pseudobulbar Palsy 33 0.131
20
DYS073 Dysphagia 51 0.129
21
MSC004 Muscle Tissue Disease 35 0.127
22
MTR014 Motor Neuron Disease 57 0.126
23
P MNN013 Meningitis 66 0.121
24
P LRY019 Laryngitis 55 0.121
25
HPT074 Hepatic Adenoma, Somatic 35 0.118
26
BRT030 Birth Defects 44 0.114
27
EXF001 Exfoliation Syndrome 56 0.111
28
MTH009 Mouth Disease 63 0.108
29
ACR041 Acromelic Frontonasal Dysostosis 45 0.107
30
CSY001 C Syndrome 49 0.105
31
PRD011 Proud Syndrome 42 0.105
32
P PLN008 Peeling Skin Syndrome 45 0.105
33
GLT021 Glutaricaciduria, Type I 47 0.103
34
INT042 Internuclear Ophthalmoplegia 36 0.102
35
HRP004 Herpes Zoster 56 0.100
36
ACD009 Acid-Labile Subunit, Deficiency of 37 0.097
37
PRG007 Progressive Bulbar Palsy 28 0.096
38
ATN002 Autonomic Nervous System Disease 46 0.095
39
HMP005 Hemiplegia 52 0.095
40
KFR001 Kufor-Rakeb Syndrome 44 0.094
41
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.094
42
P PTS002 Ptosis 56 0.092
43
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.091
44
PRP027 Peripheral Vascular Disease 69 0.091
45
P BCL006 B-Cell Lymphomas 64 0.091
46
STR067 Stroke, Ischemic 74 0.089
47
c PRK025 Parkinson Disease 10 41 0.088
48
RST001 Restless Legs Syndrome 51 0.088
49
PHY002 Physical Disorder 43 0.087
50
ART016 Aortic Aneurysm 67 0.087
51
ATN005 Autonomic Dysfunction 44 0.086
52
MVD001 Moved to 60 0.084
53
P SLP006 Sleep Apnea 60 0.084
54
SWL001 Swallowing Disorders 33 0.084
55
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.082
56
P DYS021 Dysautonomia 47 0.081
57
P SYP003 Syphilis 51 0.081
58
CNJ001 Conjugate Gaze Palsy 20 0.081
59
BNF002 Bone Fracture 46 0.080
60
VTM003 Vitamin Metabolic Disorder 31 0.080
61
LPD008 Lipid Metabolism Disorder 42 0.080
62
P HYP024 Hypoparathyroidism 52 0.079
63
PRT015 Partial Third-Nerve Palsy 23 0.079
64
BLD054 Blood Protein Disease 38 0.079
65
c PLN018 Peeling Skin Syndrome 2 36 0.078
66
TXC002 Toxic Encephalopathy 52 0.078
67
TTN003 Tetanus 62 0.078
68
P OST012 Osteoarthritis 81 0.076
69
c TRC078 Trichohepatoenteric Syndrome 2 30 0.075
70
SPC003 Specific Developmental Disorder 39 0.075
71
ADT003 Auditory System Disease 49 0.075
72
c PLN021 Peeling Skin Syndrome 3 30 0.074
73
P PRS038 Personality Disorder 60 0.073
74
c OPT055 Optic Atrophy Plus Syndrome 55 0.072
75
P OST002 Osteoporosis 63 0.072
76
P BLP003 Blepharospasm 43 0.071
77
ABL002 Ablepharon-Macrostomia Syndrome 51 0.071
78
CND002 Conduct Disorder 54 0.069
79
SXD001 Sex Differentiation Disease 39 0.068
80
ASP007 Aspiration Pneumonia 46 0.068
81
c PRK024 Parkinson Disease, Juvenile, Type 2 49 0.068
82
DRG001 Drug Psychosis 39 0.067
83
PRR007 Perry Syndrome 58 0.067
84
SBC014 Subclavian Steal Syndrome 30 0.067
85
c ESS001 Essential Tremor 58 0.067
86
P GNR027 Generalized Peeling Skin Syndrome 21 0.067
87
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 38 0.065
88
LYS021 Loeys-Dietz Syndrome 3 30 0.065
89
PSY004 Psychotic Disorder 62 0.064
90
EXT022 Exotropia 37 0.063
91
c SCN006 Secondary Syphilis 41 0.063
92
LMB012 Limb Dystonia 22 0.062
93
SPS019 Spastic Paraparesis 34 0.062
94
P PRM016 Primary Optic Atrophy 29 0.062
95
PRM157 Primary Progressive Freezing Gait 11 0.062
96
OCL003 Oculomotor Nerve Paralysis 26 0.061
97
SML020 Small Patella Syndrome 36 0.061
98
CLN006 Colonic Pseudo-Obstruction 36 0.061
99
P MTC069 Mitochondrial Disorders 51 0.060
100
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.060
101
c NMN015 Niemann-Pick Disease, Type C1 63 0.060
102
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 0.060
103
SYN058 Synucleinopathy 38 0.059
104
FXC001 Foix Chavany Marie Syndrome 22 0.058
105
NSD001 Nose Disease 51 0.058
106
c PRK022 Parkinson Disease 12 22 0.058
107
TSY001 Tau Syndrome 11 0.057
108
c PRK030 Parkinson Disease 4 38 0.057
109
BRN014 Bronchopneumonia 45 0.057
110
MTC005 Mitochondrial Metabolism Disease 37 0.056
111
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 28 0.055
112
c GCH017 Gaucher Disease, Type Iii 44 0.054
113
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.054
114
P CRB019 Cerebral Amyloid Angiopathy 56 0.053
115
VSC009 Vascular Skin Disease 21 0.053
116
c DYS033 Dysautonomia Like Disorder 18 0.052
117
P KRN004 Kernicterus 46 0.051
118
P NRC002 Narcolepsy 62 0.051
119
P GCH001 Gaucher's Disease 63 0.051
120
MSC077 Muscle Eye Brain Disease 54 0.050
121
CDS001 Cadasil 50 0.050
122
PNC056 Pineocytoma 29 0.048
123
P NMN002 Niemann-Pick Disease 63 0.048
124
c OPT023 Optic Atrophy 2 25 0.048
125
DNT016 Dentatorubro-Pallidoluysian Atrophy 49 0.047
126
c PRK059 Parkinson Disease 8 51 0.046
127
OGL001 Ogilvie Syndrome 17 0.046
128
WRN005 Wrinkles 35 0.046
129
PRM153 Primary Progressive Apraxia of Speech 9 0.045
130
SKN005 Skin Atrophy 42 0.045
131
OBS003 Obsessive-Compulsive Personality Disorder 36 0.045
132
c PRK020 Parkinson Disease 6, Early Onset 46 0.044
133
BRN097 Brainstem Auditory Evoked Responses 21 0.044
134
RCM004 Recombinant 8 Syndrome 17 0.044
135
OCL010 Ocular Hypotension 42 0.043
136
c SPN294 Spinocerebellar Ataxia 1 54 0.043
137
c ALZ014 Alzheimer Disease 16 17 0.042
138
ORM002 Oromandibular Dystonia 29 0.042
139
c OPT024 Optic Atrophy 5 18 0.041
140
THR010 Third Cranial Nerve Disease 27 0.041
141
DPB001 Deep Brain Stimulation for Parkinson's Disease 23 0.040
142
c SPS072 Spastic Ataxia 1, Autosomal Dominant 25 0.040
143
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 21 0.039
144
MNS002 Mini Stroke 18 0.037