Search results for progressive supranuclear palsy - corticobasal syndrome

159 hits were found for progressive supranuclear palsy - corticobasal syndrome

# Family MCID Name MIFTS Score
1
P SPR098 Supranuclear Palsy, Progressive 56 4.664
2
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 7 3.361
3
SPR100 Supranuclear Palsy, Progressive Atypical 28 3.061
4
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.308
5
CLS047 Classic Progressive Supranuclear Palsy Syndrome 15 1.548
6
BRN071 Brain Injury 52 0.206
7
P EPL164 Epilepsy 66 0.177
8
P LYM118 Lymphoma 69 0.176
9
P CRV039 Cervicitis 45 0.173
10
P MYP004 Myopathy 67 0.158
11
c CNT035 Central Nervous System Disease 60 0.156
12
GLB003 Globe Disease 32 0.151
13
c SPR048 Supranuclear Palsy, Progressive, 3 13 0.147
14
ANR040 Aneurysm 57 0.146
15
P ADN016 Adenocarcinoma 69 0.140
16
P CRB042 Cerebellar Ataxia 63 0.140
17
c MLT009 Multiple Cranial Nerve Palsy 33 0.139
18
P MSC033 Muscle Disorders 52 0.131
19
PSD001 Pseudobulbar Palsy 33 0.126
20
DYS073 Dysphagia 48 0.121
21
EXF001 Exfoliation Syndrome 57 0.119
22
CSY001 C Syndrome 50 0.117
23
MSC004 Muscle Tissue Disease 34 0.116
24
P LRY019 Laryngitis 54 0.115
25
MTR014 Motor Neuron Disease 58 0.114
26
P PLN008 Peeling Skin Syndrome 45 0.113
27
P MNN013 Meningitis 67 0.112
28
BRT030 Birth Defects 43 0.111
29
MTH009 Mouth Disease 61 0.107
30
ACR041 Acromelic Frontonasal Dysostosis 45 0.107
31
PRD011 Proud Syndrome 42 0.104
32
GLT021 Glutaricaciduria, Type I 46 0.103
33
EYD002 Eye Disease 61 0.102
34
INT042 Internuclear Ophthalmoplegia 37 0.097
35
ETH011 Ethylmalonic Encephalopathy 56 0.097
36
PRG007 Progressive Bulbar Palsy 30 0.095
37
ATN005 Autonomic Dysfunction 49 0.094
38
HMP005 Hemiplegia 51 0.094
39
HPT074 Hepatic Adenoma, Somatic 50 0.094
40
PRP027 Peripheral Vascular Disease 68 0.093
41
c PRK025 Parkinson Disease 10 38 0.091
42
P PTS002 Ptosis 51 0.091
43
HRP004 Herpes Zoster 56 0.091
44
PHY002 Physical Disorder 43 0.091
45
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.090
46
c PLN018 Peeling Skin Syndrome 2 40 0.090
47
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.089
48
P PRS038 Personality Disorder 62 0.089
49
HNM002 Hinman Syndrome 25 0.089
50
KFR001 Kufor-Rakeb Syndrome 44 0.087
51
P BCL006 B-Cell Lymphomas 65 0.087
52
WST001 West Syndrome 57 0.087
53
c PLN021 Peeling Skin Syndrome 3 29 0.086
54
RST001 Restless Legs Syndrome 54 0.085
55
ART016 Aortic Aneurysm 69 0.084
56
P SLP006 Sleep Apnea 61 0.083
57
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.083
58
SWL001 Swallowing Disorders 33 0.083
59
LPD008 Lipid Metabolism Disorder 58 0.082
60
ATN002 Autonomic Nervous System Disease 48 0.081
61
P OST012 Osteoarthritis 83 0.081
62
PRT015 Partial Third-Nerve Palsy 26 0.080
63
BLD054 Blood Protein Disease 37 0.080
64
P GNR027 Generalized Peeling Skin Syndrome 19 0.079
65
VTM003 Vitamin Metabolic Disorder 30 0.079
66
P DYS021 Dysautonomia 44 0.078
67
SPC003 Specific Developmental Disorder 38 0.076
68
BNF002 Bone Fracture 50 0.075
69
c PLN017 Peeling Skin Syndrome 1 34 0.075
70
c TRC078 Trichohepatoenteric Syndrome 2 29 0.074
71
CNJ001 Conjugate Gaze Palsy 29 0.073
72
ADT003 Auditory System Disease 40 0.073
73
RBR001 Roberts Syndrome 60 0.072
74
P CCK001 Cockayne Syndrome 61 0.072
75
TXC002 Toxic Encephalopathy 51 0.071
76
ADP007 Adie Pupil 34 0.069
77
ABL002 Ablepharon-Macrostomia Syndrome 57 0.069
78
c OPT055 Optic Atrophy Plus Syndrome 52 0.069
79
P OST002 Osteoporosis 64 0.069
80
P SYP003 Syphilis 53 0.068
81
P HYP024 Hypoparathyroidism 53 0.068
82
SXD001 Sex Differentiation Disease 38 0.068
83
P BLP003 Blepharospasm 43 0.067
84
OBS003 Obsessive-Compulsive Personality Disorder 36 0.067
85
c PRK022 Parkinson Disease 12 21 0.067
86
CND002 Conduct Disorder 54 0.066
87
TTN003 Tetanus 61 0.066
88
PRR007 Perry Syndrome 55 0.065
89
SBC014 Subclavian Steal Syndrome 28 0.065
90
OCL003 Oculomotor Nerve Paralysis 27 0.064
91
c ESS001 Essential Tremor 59 0.063
92
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.062
93
P PRM016 Primary Optic Atrophy 29 0.062
94
EXT022 Exotropia 39 0.061
95
PRM157 Primary Progressive Freezing Gait 13 0.060
96
SPS019 Spastic Paraparesis 41 0.060
97
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.060
98
NSD001 Nose Disease 48 0.060
99
c BNG076 Benign Exophthalmos Syndrome 15 0.060
100
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.059
101
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.059
102
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.059
103
c VRL007 Viral Encephalitis 54 0.058
104
c PRK030 Parkinson Disease 4 38 0.057
105
c NMN015 Niemann-Pick Disease, Type C1 63 0.056
106
TSY001 Tau Syndrome 10 0.056
107
c PRK059 Parkinson Disease 8 48 0.056
108
P MTC069 Mitochondrial Disorders 53 0.056
109
PSY004 Psychotic Disorder 67 0.055
110
SYN058 Synucleinopathy 38 0.054
111
FXC001 Foix Chavany Marie Syndrome 21 0.054
112
VST004 Vestibular Disease 44 0.054
113
PNC056 Pineocytoma 39 0.053
114
DRG001 Drug Psychosis 38 0.053
115
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.053
116
c GCH017 Gaucher Disease, Type Iii 46 0.053
117
CLN006 Colonic Pseudo-Obstruction 31 0.053
118
VSC009 Vascular Skin Disease 19 0.053
119
c DYS033 Dysautonomia Like Disorder 16 0.053
120
NVD002 Nevada Syndrome 14 0.051
121
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 14 0.051
122
P CRB019 Cerebral Amyloid Angiopathy 58 0.051
123
MSC077 Muscle Eye Brain Disease 57 0.050
124
P KRN004 Kernicterus 46 0.050
125
c SCN006 Secondary Syphilis 41 0.050
126
P GCH001 Gaucher's Disease 62 0.050
127
P CDS001 Cadasil 55 0.049
128
P NMN002 Niemann-Pick Disease 65 0.048
129
P NRC002 Narcolepsy 62 0.048
130
MTC005 Mitochondrial Metabolism Disease 36 0.048
131
c OPT023 Optic Atrophy 2 25 0.047
132
WDS002 Woods Syndrome 27 0.047
133
LYS021 Loeys-Dietz Syndrome 3 30 0.047
134
DNT016 Dentatorubro-Pallidoluysian Atrophy 47 0.046
135
PRM153 Primary Progressive Apraxia of Speech 11 0.046
136
THR010 Third Cranial Nerve Disease 26 0.045
137
OGL001 Ogilvie Syndrome 15 0.045
138
SML020 Small Patella Syndrome 36 0.045
139
P XRD010 Xeroderma Pigmentosum, Variant Type 58 0.045
140
SKN005 Skin Atrophy 40 0.043
141
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 47 0.043
142
RCM004 Recombinant 8 Syndrome 22 0.043
143
OCL010 Ocular Hypotension 38 0.043
144
c PRK026 Parkinson Disease 11 29 0.042
145
BRN014 Bronchopneumonia 45 0.042
146
BRN097 Brainstem Auditory Evoked Responses 22 0.042
147
c SPN294 Spinocerebellar Ataxia 1 55 0.041
148
ORM002 Oromandibular Dystonia 31 0.041
149
c ALZ014 Alzheimer Disease 16 27 0.041
150
c XRD019 Xeroderma Pigmentosum, Group C 52 0.040
151
c OPT024 Optic Atrophy 5 17 0.040
152
WRN005 Wrinkles 37 0.040
153
c PRK020 Parkinson Disease 6, Early Onset 46 0.040
154
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 28 0.039
155
c PRK070 Parkinson Disease 21 27 0.038
156
c SPS072 Spastic Ataxia 1, Autosomal Dominant 27 0.038
157
P XRD027 Xeroderma Pigmentosum Group E 35 0.038
158
c PRK052 Parkinson Disease 17 29 0.036
159
MNS002 Mini Stroke 19 0.036
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