Search results for "tauopathy"

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

115 hits were found for 'tauopathy'

# Family MCID Name MIFTS Score
1
P DMN033 Dementia, Frontotemporal 62 4.868
2
MPT001 Mapt-Related Disorders 16 4.720
3
NRN002 Neuronitis 41 0.329
4
DMN002 Dementia 65 0.304
5
P ALZ034 Alzheimer Disease 92 0.206
6
P CRT033 Corticobasal Degeneration 47 0.192
7
SYN058 Synucleinopathy 38 0.171
8
BRN071 Brain Injury 52 0.146
9
P AMY004 Amyloidosis 65 0.136
10
P SPR098 Supranuclear Palsy, Progressive 56 0.136
11
CRB037 Cerebral Palsy 66 0.126
12
KRN002 Kearns-Sayre Syndrome 61 0.126
13
P ENC018 Encephalopathy 59 0.126
14
APH002 Aphasia 54 0.126
15
OPT006 Optic Nerve Disease 52 0.126
16
MVM001 Movement Disease 49 0.126
17
P CRN035 Cranial Nerve Palsy 46 0.126
18
BSL008 Basal Ganglia Disease 40 0.126
19
CRN031 Cranial Nerve Disease 40 0.126
20
OCL011 Ocular Motility Disease 37 0.126
21
FST001 Foster-Kennedy Syndrome 31 0.126
22
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.126
23
SPR038 Supranuclear Ocular Palsy 15 0.126
24
PCK002 Pick Disease 68 0.115
25
MTR014 Motor Neuron Disease 58 0.115
26
P LTR001 Lateral Sclerosis 53 0.115
27
TRM010 Traumatic Brain Injury 52 0.115
28
CRB009 Cerebritis 39 0.115
29
GLB003 Globe Disease 32 0.115
30
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.103
31
HDN002 Head Injury 45 0.103
32
CRB033 Cerebral Degeneration 44 0.103
33
SMN008 Semantic Dementia 44 0.103
34
EYD001 Eye Degenerative Disease 30 0.103
35
TSY001 Tau Syndrome 10 0.103
36
ISC004 Ischemia 61 0.089
37
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.089
38
GLT021 Glutaricaciduria, Type I 46 0.089
39
SPC010 Speech and Communication Disorders 41 0.089
40
SPC005 Speech Disorder 41 0.089
41
c GRN014 Grn-Related Frontotemporal Dementia 40 0.089
42
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.089
43
c ALZ032 Alzheimer Disease 18 35 0.089
44
c MLT009 Multiple Cranial Nerve Palsy 33 0.089
45
FRN030 Frontotemporal Dementia with Parkinsonism-17 29 0.089
46
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.089
47
c SPR049 Supranuclear Palsy, Progressive, 2 18 0.089
48
MLT021 Multiple System Atrophy 70 0.073
49
P PRK057 Parkinson Disease, Late-Onset 70 0.073
50
P SHR029 Short Syndrome 58 0.073
51
EXF001 Exfoliation Syndrome 57 0.073
52
TRN015 Transient Cerebral Ischemia 56 0.073
53
c PRK031 Parkinson Disease 1 51 0.073
54
P PLN008 Peeling Skin Syndrome 45 0.073
55
HMM003 Hemimegalencephaly 45 0.073
56
P CRB088 Cerebral Atrophy 43 0.073
57
RMS001 Rem Sleep Behavior Disorder 41 0.073
58
c PLN018 Peeling Skin Syndrome 2 40 0.073
59
ADR009 Adrenal Cortex Disease 39 0.073
60
c PLN017 Peeling Skin Syndrome 1 34 0.073
61
OCL003 Oculomotor Nerve Paralysis 27 0.073
62
PRG033 Progressive Non-Fluent Aphasia 27 0.073
63
PRT015 Partial Third-Nerve Palsy 26 0.073
64
P GNR027 Generalized Peeling Skin Syndrome 19 0.073
65
P OBS005 Obesity 92 0.051
66
P RSP003 Respiratory Failure 71 0.051
67
P TBR001 Tuberous Sclerosis 67 0.051
68
P EPL164 Epilepsy 66 0.051
69
INC002 Inclusion Body Myositis 66 0.051
70
P MSC005 Muscular Dystrophy 65 0.051
71
CNT098 Central Core Disease 65 0.051
72
P CRT072 Creutzfeldt-Jakob Disease 61 0.051
73
CRB011 Cerebrotendinous Xanthomatosis 61 0.051
74
WLL006 Wells Syndrome 59 0.051
75
P MYS005 Myositis 57 0.051
76
HYP266 Hypoxia 56 0.051
77
P RTN016 Retinal Degeneration 54 0.051
78
P TRM003 Tremor 54 0.051
79
SLP005 Sleep Disorder 53 0.051
80
OLV001 Olivopontocerebellar Atrophy 53 0.051
81
RTN018 Retinal Disease 53 0.051
82
P ATX004 Ataxia 53 0.051
83
LYS002 Lysosomal Storage Disease 52 0.051
84
c OPT055 Optic Atrophy Plus Syndrome 52 0.051
85
GNG004 Ganglioglioma 50 0.051
86
CSY001 C Syndrome 50 0.051
87
ATN005 Autonomic Dysfunction 49 0.051
88
P MYT002 Myotonic Dystrophy 48 0.051
89
NSD001 Nose Disease 48 0.051
90
ATN002 Autonomic Nervous System Disease 48 0.051
91
VND001 Vein Disease 47 0.051
92
CRB027 Cerebellar Disease 47 0.051
93
XNT003 Xanthomatosis 46 0.051
94
GDS001 Good Syndrome 44 0.051
95
P DYS021 Dysautonomia 44 0.051
96
AMN003 Amnestic Disorder 43 0.051
97
c OPT053 Optic Atrophy 1 43 0.051
98
SPS057 Spasticity 42 0.051
99
c ALZ042 Alzheimer's Disease 14 40 0.051
100
c PRK025 Parkinson Disease 10 38 0.051
101
SPC003 Specific Developmental Disorder 38 0.051
102
NSY001 N Syndrome 36 0.051
103
NTR005 Nutritional Deficiency Disease 36 0.051
104
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.051
105
P CHR084 Chromosomal Disease 32 0.051
106
PST086 Posterior Cortical Atrophy 32 0.051
107
c PRK051 Parkinson Disease 18 30 0.051
108
c PRK052 Parkinson Disease 17 29 0.051
109
P PRM016 Primary Optic Atrophy 29 0.051
110
c OPT023 Optic Atrophy 2 25 0.051
111
c PRK022 Parkinson Disease 12 21 0.051
112
c OPT025 Optic Atrophy 6 20 0.051
113
c OPT064 Optic Atrophy 11 18 0.051
114
c DYS033 Dysautonomia Like Disorder 16 0.051
115
ALZ007 Alzheimer's Disease Without Neurofibrillary Tangles 8 0.051