Search results for "tauopathy"

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

114 hits were found for 'tauopathy'

# Family MCID Name MIFTS Score
1
P DMN033 Dementia, Frontotemporal 63 4.860
2
MPT001 Mapt-Related Disorders 17 4.713
3
NRN002 Neuronitis 42 0.329
4
DMN002 Dementia 64 0.304
5
P ALZ034 Alzheimer Disease 93 0.206
6
P CRT033 Corticobasal Degeneration 46 0.192
7
SYN058 Synucleinopathy 39 0.170
8
BRN071 Brain Injury 52 0.145
9
P AMY004 Amyloidosis 64 0.136
10
P SPR098 Supranuclear Palsy, Progressive 58 0.136
11
KRN002 Kearns-Sayre Syndrome 59 0.126
12
P ENC018 Encephalopathy 59 0.126
13
CRB037 Cerebral Palsy 54 0.126
14
MVM001 Movement Disease 54 0.126
15
APH002 Aphasia 53 0.126
16
OPT006 Optic Nerve Disease 51 0.126
17
P CRN035 Cranial Nerve Palsy 43 0.126
18
BSL008 Basal Ganglia Disease 43 0.126
19
CRN031 Cranial Nerve Disease 40 0.126
20
OCL011 Ocular Motility Disease 38 0.126
21
FST001 Foster-Kennedy Syndrome 34 0.126
22
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.126
23
SPR038 Supranuclear Ocular Palsy 20 0.126
24
PCK002 Pick Disease 67 0.115
25
MTR014 Motor Neuron Disease 59 0.115
26
TRM010 Traumatic Brain Injury 52 0.115
27
P LTR001 Lateral Sclerosis 52 0.115
28
CRB009 Cerebritis 38 0.115
29
GLB003 Globe Disease 35 0.115
30
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.103
31
CRB033 Cerebral Degeneration 46 0.103
32
HDN002 Head Injury 45 0.103
33
SMN008 Semantic Dementia 44 0.103
34
EYD001 Eye Degenerative Disease 31 0.103
35
TSY001 Tau Syndrome 12 0.103
36
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 60 0.089
37
ISC004 Ischemia 59 0.089
38
GLT021 Glutaricaciduria, Type I 48 0.089
39
SPC010 Speech and Communication Disorders 46 0.089
40
c GRN014 Grn-Related Frontotemporal Dementia 43 0.089
41
SPC005 Speech Disorder 43 0.089
42
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.089
43
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.089
44
c MLT009 Multiple Cranial Nerve Palsy 31 0.089
45
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.089
46
c ALZ032 Alzheimer Disease 18 26 0.089
47
c SPR049 Supranuclear Palsy, Progressive, 2 20 0.089
48
P PRK057 Parkinson Disease, Late-Onset 72 0.073
49
MLT021 Multiple System Atrophy 71 0.073
50
P SHR029 Short Syndrome 60 0.073
51
EXF001 Exfoliation Syndrome 57 0.073
52
TRN015 Transient Cerebral Ischemia 56 0.073
53
c PRK031 Parkinson Disease 1 55 0.073
54
P PLN008 Peeling Skin Syndrome 47 0.073
55
HMM003 Hemimegalencephaly 45 0.073
56
P CRB088 Cerebral Atrophy 42 0.073
57
ADR009 Adrenal Cortex Disease 41 0.073
58
RMS001 Rem Sleep Behavior Disorder 40 0.073
59
c PLN018 Peeling Skin Syndrome 2 35 0.073
60
c PLN017 Peeling Skin Syndrome 1 33 0.073
61
OCL003 Oculomotor Nerve Paralysis 27 0.073
62
PRT015 Partial Third-Nerve Palsy 27 0.073
63
P GNR027 Generalized Peeling Skin Syndrome 22 0.073
64
PRG033 Progressive Non-Fluent Aphasia 19 0.073
65
P OBS005 Obesity 93 0.051
66
P RSP003 Respiratory Failure 70 0.051
67
CNT098 Central Core Disease 66 0.051
68
P EPL164 Epilepsy 66 0.051
69
P MSC005 Muscular Dystrophy 64 0.051
70
P CRT072 Creutzfeldt-Jakob Disease 63 0.051
71
INC002 Inclusion Body Myositis 63 0.051
72
P SPN301 Spinocerebellar Ataxia 2 63 0.051
73
CRB011 Cerebrotendinous Xanthomatosis 60 0.051
74
WLL006 Wells Syndrome 56 0.051
75
RTN018 Retinal Disease 56 0.051
76
P MYS005 Myositis 56 0.051
77
HYP266 Hypoxia 55 0.051
78
c OPT055 Optic Atrophy Plus Syndrome 54 0.051
79
P TRM003 Tremor 54 0.051
80
P RTN016 Retinal Degeneration 54 0.051
81
SLP005 Sleep Disorder 53 0.051
82
P ATX004 Ataxia 53 0.051
83
LYS002 Lysosomal Storage Disease 52 0.051
84
VND001 Vein Disease 52 0.051
85
NSD001 Nose Disease 52 0.051
86
LRN003 Learning Disability 51 0.051
87
CSY001 C Syndrome 49 0.051
88
GNG004 Ganglioglioma 49 0.051
89
P DYS021 Dysautonomia 47 0.051
90
P MYT002 Myotonic Dystrophy 47 0.051
91
XNT003 Xanthomatosis 47 0.051
92
CRB027 Cerebellar Disease 47 0.051
93
ATN002 Autonomic Nervous System Disease 47 0.051
94
c OPT053 Optic Atrophy 1 46 0.051
95
AMN003 Amnestic Disorder 46 0.051
96
ATN005 Autonomic Dysfunction 45 0.051
97
GDS001 Good Syndrome 45 0.051
98
SPS057 Spasticity 42 0.051
99
c PRK025 Parkinson Disease 10 42 0.051
100
SPC003 Specific Developmental Disorder 40 0.051
101
NTR005 Nutritional Deficiency Disease 39 0.051
102
NSY001 N Syndrome 39 0.051
103
c ALZ042 Alzheimer's Disease 14 37 0.051
104
P CHR084 Chromosomal Disease 37 0.051
105
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.051
106
PST086 Posterior Cortical Atrophy 35 0.051
107
P PRM016 Primary Optic Atrophy 32 0.051
108
c PRK051 Parkinson Disease 18 31 0.051
109
c PRK052 Parkinson Disease 17 28 0.051
110
c OPT023 Optic Atrophy 2 27 0.051
111
c PRK022 Parkinson Disease 12 24 0.051
112
c OPT025 Optic Atrophy 6 22 0.051
113
c DYS033 Dysautonomia Like Disorder 19 0.051
114
ALZ007 Alzheimer's Disease Without Neurofibrillary Tangles 8 0.051