Search results for "[genes] TARDBP"

54 hits were found for '[genes] TARDBP'

# Family MCID Name MIFTS Score
1
P LTR001 Lateral Sclerosis 50 16.803
2
c AMY091 Amyotrophic Lateral Sclerosis 1 78 15.339
3
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 25 13.720
4
c TRD001 Tardbp-Related Amyotrophic Lateral Sclerosis 12 13.720
5
P ALZ034 Alzheimer Disease 92 11.882
6
INC002 Inclusion Body Myositis 64 11.882
7
CYS001 Cystic Fibrosis 87 11.882
8
P DMN033 Dementia, Frontotemporal 63 11.882
9
HV1006 Hiv-1 80 11.882
10
PCK002 Pick Disease 66 11.882
11
PRR007 Perry Syndrome 58 11.882
12
P MYS005 Myositis 57 11.882
13
SPC010 Speech and Communication Disorders 42 11.882
14
c AMY019 Amyotrophic Lateral Sclerosis Type 10 31 11.882
15
MTR014 Motor Neuron Disease 57 11.882
16
FTD003 Ftdals1 28 11.882
17
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 9.701
18
DMN031 Dementia, Lewy Body 58 9.701
19
c LTH007 Lethal Congenital Contracture Syndrome 1 38 9.701
20
c SPN265 Spinocerebellar Ataxia 36 43 9.701
21
PST020 Postpoliomyelitis Syndrome 38 9.701
22
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 9.701
23
c AMY085 Amyotrophic Lateral Sclerosis 9 41 9.701
24
c SPN305 Spinocerebellar Ataxia 11 40 9.701
25
c AMY083 Amyotrophic Lateral Sclerosis 11 37 9.701
26
ADL060 Adult Polyglucosan Body Disease 30 9.701
27
c AMY067 Amyotrophic Lateral Sclerosis 18 38 9.701
28
c AMY069 Amyotrophic Lateral Sclerosis 21 40 9.701
29
c AMY023 Amyotrophic Lateral Sclerosis Type 6 36 9.701
30
c CNT035 Central Nervous System Disease 60 9.701
31
ALX001 Alexia 42 9.701
32
c AMY089 Amyotrophic Lateral Sclerosis 7 33 9.701
33
BRW001 Brown-Vialetto-Van Laere Syndrome 30 9.701
34
P PRS013 Prosopagnosia 40 9.701
35
PST027 Postencephalitic Parkinson Disease 24 9.701
36
SMN008 Semantic Dementia 43 9.701
37
EXP001 Expressive Language Disorder 28 9.701
38
NMN001 Nominal Aphasia 28 9.701
39
IDM001 Ideomotor Apraxia 34 9.701
40
AGR018 Agraphia 38 9.701
41
AKN002 Akinetic Mutism 36 9.701
42
P CRT033 Corticobasal Degeneration 44 9.701
43
BSL008 Basal Ganglia Disease 40 9.701
44
c PRG001 Progressive Muscular Atrophy 39 9.701
45
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 23 9.701
46
c AMY074 Amyotrophic Lateral Sclerosis Type 14 24 9.701
47
ANT007 Anterior Horn Cell Disease 29 9.701
48
ART010 Arteriolosclerosis 26 9.701
49
MTR013 Motor Neuritis 29 9.701
50
PHN002 Phonagnosia 18 9.701
51
ASS001 Associative Agnosia 18 9.701
52
CRT078 Corticobasal Syndrome 36 9.701
53
P NRV007 Nervous System Disease 71 6.860
54
c TRD005 Tardbp-Related Frontotemporal Dementia 8 6.860