Search results for "[genes] TARDBP"

53 hits were found for '[genes] TARDBP'

# Family MCID Name MIFTS Score
1
P LTR001 Lateral Sclerosis 52 16.843
2
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 41 16.843
3
c AMY091 Amyotrophic Lateral Sclerosis 1 78 15.375
4
PCK002 Pick Disease 67 13.752
5
P DMN033 Dementia, Frontotemporal 63 13.752
6
MTR014 Motor Neuron Disease 59 13.752
7
c TRD001 Tardbp-Related Amyotrophic Lateral Sclerosis 12 13.752
8
P ALZ034 Alzheimer Disease 93 11.910
9
CYS001 Cystic Fibrosis 86 11.910
10
HV1006 Hiv-1 82 11.910
11
DMN002 Dementia 64 11.910
12
INC002 Inclusion Body Myositis 63 11.910
13
PRR007 Perry Syndrome 57 11.910
14
SPC010 Speech and Communication Disorders 46 11.910
15
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 41 11.910
16
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 60 9.724
17
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 9.724
18
P CRT033 Corticobasal Degeneration 46 9.724
19
ALX001 Alexia 45 9.724
20
SMN008 Semantic Dementia 44 9.724
21
c SPN265 Spinocerebellar Ataxia 36 43 9.724
22
BSL008 Basal Ganglia Disease 43 9.724
23
c AMY085 Amyotrophic Lateral Sclerosis 9 41 9.724
24
c SPN305 Spinocerebellar Ataxia 11 41 9.724
25
c PRG001 Progressive Muscular Atrophy 40 9.724
26
c AMY069 Amyotrophic Lateral Sclerosis 21 40 9.724
27
PST020 Postpoliomyelitis Syndrome 39 9.724
28
AGR018 Agraphia 39 9.724
29
c AMY067 Amyotrophic Lateral Sclerosis 18 39 9.724
30
c LTH007 Lethal Congenital Contracture Syndrome 1 38 9.724
31
LCK001 Locked-in Syndrome 38 9.724
32
DYS003 Dysgraphia 38 9.724
33
IDM001 Ideomotor Apraxia 36 9.724
34
c AMY083 Amyotrophic Lateral Sclerosis 11 36 9.724
35
NMN001 Nominal Aphasia 33 9.724
36
P LTH003 Lethal Congenital Contracture Syndrome 33 9.724
37
c AMY089 Amyotrophic Lateral Sclerosis 7 32 9.724
38
AMY095 Amyotrophic Lateral Sclerosis 6, with or Without Frontotemporal Dementia 32 9.724
39
EXP001 Expressive Language Disorder 29 9.724
40
ADL060 Adult Polyglucosan Body Disease 29 9.724
41
BRW001 Brown-Vialetto-Van Laere Syndrome 29 9.724
42
WRT002 Writing Disorder 29 9.724
43
ANT007 Anterior Horn Cell Disease 28 9.724
44
ART010 Arteriolosclerosis 28 9.724
45
PST027 Postencephalitic Parkinson Disease 24 9.724
46
c AMY074 Amyotrophic Lateral Sclerosis Type 14 24 9.724
47
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 23 9.724
48
ASS001 Associative Agnosia 18 9.724
49
PHN002 Phonagnosia 17 9.724
50
P NRV007 Nervous System Disease 71 6.876
51
DMN031 Dementia, Lewy Body 60 6.876
52
c CNT035 Central Nervous System Disease 59 6.876
53
c TRD005 Tardbp-Related Frontotemporal Dementia 8 6.876