Search results for progressive supranuclear palsy - corticobasal syndrome

183 hits were found for progressive supranuclear palsy - corticobasal syndrome

# Family MCID Name MIFTS Score
1
PRK087 Parkinson-Dementia Syndrome 30 6.412
2
P SPR120 Supranuclear Palsy, Progressive, 1 70 5.022
3
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 8 3.363
4
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 7 2.310
5
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 1.549
6
P NRP001 Neuropathy 63 0.269
7
c CNT035 Central Nervous System Disease 65 0.238
8
BRN071 Brain Injury 54 0.219
9
SPR038 Supranuclear Ocular Palsy 21 0.215
10
P LYM118 Lymphoma 71 0.213
11
P CRN035 Cranial Nerve Palsy 42 0.207
12
P EPL164 Epilepsy 70 0.205
13
P CRV039 Cervicitis 49 0.204
14
c BLD140 Blood Group, I System 37 0.184
15
P MLT020 Multiple Sclerosis 85 0.182
16
RTN023 Retinitis 52 0.182
17
ANR040 Aneurysm 61 0.182
18
P ADN016 Adenocarcinoma 71 0.174
19
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.156
20
P SCL018 Scoliosis 56 0.150
21
P MNN013 Meningitis 71 0.144
22
ACR006 Aceruloplasminemia 65 0.142
23
PSD001 Pseudobulbar Palsy 35 0.141
24
P LRY019 Laryngitis 57 0.139
25
c BRN108 Branchiootic Syndrome 1 47 0.139
26
MTR014 Motor Neuron Disease 62 0.131
27
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.129
28
ANX010 Anxiety 72 0.124
29
HPT082 Hepatic Adenomas, Familial 52 0.122
30
FCL012 Facial Paralysis 50 0.118
31
RST001 Restless Legs Syndrome 54 0.118
32
INT042 Internuclear Ophthalmoplegia 40 0.117
33
P SLP006 Sleep Apnea 65 0.114
34
ATN005 Autonomic Dysfunction 51 0.111
35
P BCL006 B-Cell Lymphomas 70 0.111
36
NRM005 Neuromuscular Disease 60 0.110
37
ART016 Aortic Aneurysm 70 0.110
38
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.108
39
KFR001 Kufor-Rakeb Syndrome 42 0.104
40
P MYP006 Myopia 56 0.103
41
P PTS002 Ptosis 50 0.102
42
P PRS038 Personality Disorder 65 0.101
43
HMP005 Hemiplegia 54 0.101
44
P DYS021 Dysautonomia 47 0.101
45
P RTN016 Retinal Degeneration 56 0.099
46
P BLP003 Blepharospasm 46 0.098
47
HRP004 Herpes Zoster 61 0.097
48
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.095
49
SBC014 Subclavian Steal Syndrome 31 0.095
50
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 35 0.095
51
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 35 0.095
52
P HYP024 Hypoparathyroidism 55 0.093
53
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.091
54
PRR007 Perry Syndrome 51 0.091
55
MBS002 Moebius Syndrome 53 0.091
56
P HMN010 Hemangioma 61 0.089
57
EST005 Esotropia 43 0.089
58
MLL002 Miller Fisher Syndrome 44 0.088
59
SPC010 Speech and Communication Disorders 40 0.087
60
P KRT007 Keratoconus 49 0.086
61
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.086
62
c ESS001 Essential Tremor 58 0.085
63
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.084
64
P RSP003 Respiratory Failure 71 0.084
65
SPC005 Speech Disorder 44 0.083
66
OBS003 Obsessive-Compulsive Personality Disorder 29 0.082
67
BNF002 Bone Fracture 56 0.082
68
P SYP003 Syphilis 55 0.082
69
SPS019 Spastic Paraparesis 33 0.081
70
CRB039 Cerebrovascular Disease 68 0.081
71
CHR073 Choreatic Disease 40 0.081
72
OST012 Osteoarthritis 88 0.080
73
HDN002 Head Injury 48 0.080
74
ADP007 Adie Pupil 41 0.079
75
LSC001 Lesch-Nyhan Syndrome 62 0.079
76
CLN006 Colonic Pseudo-Obstruction 36 0.078
77
P MJR001 Major Depressive Disorder 70 0.078
78
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.078
79
NRG002 Neurogenic Bladder 53 0.078
80
PRM153 Primary Progressive Apraxia of Speech 21 0.077
81
c PRG001 Progressive Muscular Atrophy 41 0.077
82
SPN331 Spondyloocular Syndrome 34 0.077
83
EXT022 Exotropia 41 0.076
84
SYN058 Synucleinopathy 42 0.075
85
P TRT019 Torticollis 45 0.075
86
P OST002 Osteoporosis 75 0.074
87
P NMN002 Niemann-Pick Disease 68 0.073
88
CNJ001 Conjugate Gaze Palsy 30 0.073
89
OGL001 Ogilvie Syndrome 20 0.072
90
PNC056 Pineocytoma 49 0.071
91
c TRC078 Trichohepatoenteric Syndrome 2 34 0.071
92
c GCH017 Gaucher Disease, Type Iii 47 0.071
93
SWL001 Swallowing Disorders 36 0.071
94
CNV002 Conversion Disorder 42 0.070
95
CGN007 Cognitive Function 1, Social 27 0.070
96
c NMN015 Niemann-Pick Disease, Type C1 57 0.070
97
BRN014 Bronchopneumonia 45 0.069
98
BRW001 Brown-Vialetto-Van Laere Syndrome 27 0.069
99
TTN003 Tetanus 65 0.069
100
HYP052 Hyperkalemic Periodic Paralysis 57 0.069
101
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.069
102
P MCH002 Machado-Joseph Disease 63 0.068
103
WRN002 Wernicke-Korsakoff Syndrome 52 0.068
104
BRN097 Brainstem Auditory Evoked Responses 24 0.068
105
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 18 0.068
106
WRN005 Wrinkles 41 0.067
107
ORM002 Oromandibular Dystonia 32 0.066
108
c ART101 Aortic Valve Disease 2 65 0.066
109
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.066
110
IDP070 Idiopathic Scoliosis 42 0.065
111
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.065
112
P NRM001 Neuromyelitis Optica 67 0.064
113
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.063
114
c SCN006 Secondary Syphilis 40 0.063
115
P NRC002 Narcolepsy 64 0.062
116
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.062
117
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.062
118
SPS134 Spasmodic Dystonia 20 0.061
119
PSY004 Psychotic Disorder 72 0.061
120
SPN041 Spinal Cord Disease 54 0.061
121
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 50 0.060
122
MTS001 Mutism 42 0.059
123
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 31 0.059
124
c SPN294 Spinocerebellar Ataxia 1 58 0.058
125
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.057
126
AND005 Androgen Insensitivity Syndrome, Mild 16 0.057
127
c SPL067 Split-Hand/foot Malformation 1 40 0.056
128
FXC001 Foix Chavany Marie Syndrome 24 0.056
129
ATN002 Autonomic Nervous System Disease 51 0.056
130
c MYP021 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 37 0.054
131
c SRC023 Sarcoidosis 2 30 0.054
132
OST006 Osteoblastoma 32 0.053
133
P EPS003 Episodic Ataxia 57 0.053
134
VSC002 Vascular Dementia 58 0.052
135
P KRN004 Kernicterus 48 0.052
136
c SPS203 Spastic Paraplegia 78, Autosomal Recessive 27 0.051
137
P ATR001 Atrioventricular Septal Defect 56 0.051
138
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 33 0.051
139
KLV001 Kluver-Bucy Syndrome 41 0.050
140
CVR006 Cavernous Hemangioma 48 0.050
141
P GCH001 Gaucher's Disease 62 0.050
142
c NRM008 Neuromyelitis Optica Spectrum Disorder 30 0.050
143
ALX001 Alexia 44 0.050
144
c VRL007 Viral Encephalitis 53 0.049
145
MGC001 Megacolon 50 0.049
146
LYS021 Loeys-Dietz Syndrome 3 33 0.049
147
P PRS013 Prosopagnosia 34 0.048
148
CCN002 Cocaine Abuse 50 0.047
149
TXC002 Toxic Encephalopathy 55 0.047
150
GNG005 Gangliocytoma 50 0.047
151
ESN006 Eosinophilic Meningitis 38 0.047
152
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 49 0.046
153
P MCL013 Mucolipidosis Iv 67 0.046
154
c AMY069 Amyotrophic Lateral Sclerosis 21 39 0.046
155
P SBS003 Substance Abuse 57 0.046
156
c EPS035 Episodic Ataxia, Type 2 54 0.045
157
AKN002 Akinetic Mutism 33 0.045
158
DSS008 Disease of Mental Health 51 0.044
159
PRT058 Pure Autonomic Failure 60 0.044
160
c ERL020 Early-Onset Schizophrenia 51 0.044
161
BNS003 Binswanger's Disease 43 0.043
162
NMN001 Nominal Aphasia 36 0.043
163
IMP006 Impulse Control Disorder 43 0.043
164
c SPN104 Spinocerebellar Ataxia 34 32 0.043
165
ECH002 Echolalia 35 0.041
166
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 30 0.041
167
AMN003 Amnestic Disorder 45 0.040
168
P FML043 Familial Idiopathic Basal Ganglia Calcification 40 0.040
169
DLS001 Delusional Disorder 41 0.040
170
BHV002 Behavioral Variant of Frontotemporal Dementia 41 0.040
171
WRT002 Writing Disorder 23 0.040
172
c AMY067 Amyotrophic Lateral Sclerosis 18 38 0.039
173
GTP001 Gait Apraxia 38 0.039
174
c ALZ049 Alzheimer Disease 2 59 0.039
175
NRN008 Neuronal Intranuclear Inclusion Disease 44 0.039
176
PHN002 Phonagnosia 18 0.039
177
TND006 Tendinosis 43 0.039
178
SNL009 Senile Plaque Formation 26 0.038
179
ASS001 Associative Agnosia 18 0.038
180
c ERL006 Early-Onset Familial Alzheimer Disease 38 0.038
181
HYP572 Hypoganglionosis 31 0.037
182
EXP001 Expressive Language Disorder 24 0.036
183
ALC013 Alcohol-Induced Mental Disorder 23 0.036
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