Search results for "[genes] TARDBP"

54 hits were found for '[genes] TARDBP'

# Family MCID Name MIFTS Score
1
P LTR001 Lateral Sclerosis 56 16.892
2
c AMY091 Amyotrophic Lateral Sclerosis 1 79 15.420
3
PCK002 Pick Disease 65 13.792
4
MTR014 Motor Neuron Disease 61 13.792
5
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 28 13.792
6
c TRD001 Tardbp-Related Amyotrophic Lateral Sclerosis 15 13.792
7
P ALZ034 Alzheimer Disease 94 11.944
8
CYS001 Cystic Fibrosis 86 11.944
9
HV1006 Hiv-1 82 11.944
10
INC002 Inclusion Body Myositis 65 11.944
11
DMN002 Dementia 64 11.944
12
P DMN033 Dementia, Frontotemporal 62 11.944
13
PRR007 Perry Syndrome 58 11.944
14
SPC010 Speech and Communication Disorders 45 11.944
15
FTD003 Ftdals1 30 11.944
16
c AMY019 Amyotrophic Lateral Sclerosis Type 10 28 11.944
17
DMN031 Dementia, Lewy Body 60 9.753
18
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 51 9.753
19
ALX001 Alexia 48 9.753
20
P NRL007 Neurologic Diseases 48 9.753
21
SMN008 Semantic Dementia 46 9.753
22
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 45 9.753
23
P PRS013 Prosopagnosia 43 9.753
24
c PRG001 Progressive Muscular Atrophy 43 9.753
25
c AMY069 Amyotrophic Lateral Sclerosis 21 43 9.753
26
c AMY085 Amyotrophic Lateral Sclerosis 9 41 9.753
27
P CRT033 Corticobasal Degeneration 41 9.753
28
BSL008 Basal Ganglia Disease 40 9.753
29
c AMY067 Amyotrophic Lateral Sclerosis 18 40 9.753
30
LCK001 Locked-in Syndrome 40 9.753
31
c SPN265 Spinocerebellar Ataxia 36 40 9.753
32
PST020 Postpoliomyelitis Syndrome 39 9.753
33
AKN002 Akinetic Mutism 38 9.753
34
AGR018 Agraphia 38 9.753
35
c AMY089 Amyotrophic Lateral Sclerosis 7 38 9.753
36
c SPN305 Spinocerebellar Ataxia 11 37 9.753
37
c MYP078 Myopathy, Myofibrillar, 3 37 9.753
38
IDM001 Ideomotor Apraxia 37 9.753
39
ADL060 Adult Polyglucosan Body Disease 36 9.753
40
c AMY023 Amyotrophic Lateral Sclerosis Type 6 35 9.753
41
BRW001 Brown-Vialetto-Van Laere Syndrome 35 9.753
42
c AMY083 Amyotrophic Lateral Sclerosis 11 35 9.753
43
ANT007 Anterior Horn Cell Disease 34 9.753
44
NMN001 Nominal Aphasia 33 9.753
45
EXP001 Expressive Language Disorder 32 9.753
46
PST027 Postencephalitic Parkinson Disease 31 9.753
47
c AMY074 Amyotrophic Lateral Sclerosis Type 14 28 9.753
48
MTR013 Motor Neuritis 25 9.753
49
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 24 9.753
50
ASS001 Associative Agnosia 21 9.753
51
PHN002 Phonagnosia 19 9.753
52
P NRV007 Nervous System Disease 70 6.896
53
c CNT035 Central Nervous System Disease 61 6.896
54
c TRD005 Tardbp-Related Frontotemporal Dementia 6 6.896