Search results for "[genes] TARDBP"

56 hits were found for '[genes] TARDBP'

# Family MCID Name MIFTS Score
1
c AMY091 Amyotrophic Lateral Sclerosis 1 78 16.749
2
P LTR001 Lateral Sclerosis 53 16.749
3
PCK002 Pick Disease 68 15.290
4
DMN002 Dementia 65 15.290
5
P DMN033 Dementia, Frontotemporal 62 15.290
6
MTR014 Motor Neuron Disease 58 15.290
7
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 33 15.290
8
P ALZ034 Alzheimer Disease 92 13.675
9
CYS001 Cystic Fibrosis 83 13.675
10
HV1006 Hiv-1 80 13.675
11
INC002 Inclusion Body Myositis 66 13.675
12
PRR007 Perry Syndrome 55 13.675
13
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 13.675
14
SPC010 Speech and Communication Disorders 41 13.675
15
c TRD001 Tardbp-Related Amyotrophic Lateral Sclerosis 12 13.675
16
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 11.843
17
DMN031 Dementia, Lewy Body 58 11.843
18
APH002 Aphasia 54 11.843
19
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 11.843
20
P CRT033 Corticobasal Degeneration 47 11.843
21
SMN008 Semantic Dementia 44 11.843
22
c SPN305 Spinocerebellar Ataxia 11 42 11.843
23
c SPN265 Spinocerebellar Ataxia 36 42 11.843
24
c AMY067 Amyotrophic Lateral Sclerosis 18 41 11.843
25
c AMY085 Amyotrophic Lateral Sclerosis 9 41 11.843
26
ALX001 Alexia 40 11.843
27
BSL008 Basal Ganglia Disease 40 11.843
28
c PRG001 Progressive Muscular Atrophy 39 11.843
29
LCK001 Locked-in Syndrome 38 11.843
30
c AMY069 Amyotrophic Lateral Sclerosis 21 38 11.843
31
PST020 Postpoliomyelitis Syndrome 38 11.843
32
c LTH007 Lethal Congenital Contracture Syndrome 1 38 11.843
33
c AMY083 Amyotrophic Lateral Sclerosis 11 37 11.843
34
IDM001 Ideomotor Apraxia 36 11.843
35
AGR018 Agraphia 36 11.843
36
DYS003 Dysgraphia 36 11.843
37
NMN001 Nominal Aphasia 33 11.843
38
ADL060 Adult Polyglucosan Body Disease 33 11.843
39
AMY095 Amyotrophic Lateral Sclerosis 6, with or Without Frontotemporal Dementia 32 11.843
40
c AMY089 Amyotrophic Lateral Sclerosis 7 31 11.843
41
BRW001 Brown-Vialetto-Van Laere Syndrome 30 11.843
42
EXP001 Expressive Language Disorder 29 11.843
43
ANT007 Anterior Horn Cell Disease 27 11.843
44
WRT002 Writing Disorder 27 11.843
45
ART010 Arteriolosclerosis 27 11.843
46
PST027 Postencephalitic Parkinson Disease 26 11.843
47
c AMY074 Amyotrophic Lateral Sclerosis Type 14 25 11.843
48
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 20 11.843
49
ASS001 Associative Agnosia 17 11.843
50
PHN002 Phonagnosia 17 11.843
51
c TRD005 Tardbp-Related Frontotemporal Dementia 8 11.843
52
P NRV007 Nervous System Disease 71 9.670
53
c CNT035 Central Nervous System Disease 60 9.670
54
c SPN103 Spinocerebellar Ataxia 31 38 9.670
55
c AMY019 Amyotrophic Lateral Sclerosis Type 10 31 9.670
56
HYP695 Hypertrichotic Osteochondrodysplasia Cantu Type 24 9.670