Search results for "[genes] TARDBP"

48 hits were found for '[genes] TARDBP'

# Family MCID Name MIFTS Score
1
c AMY091 Amyotrophic Lateral Sclerosis 1 83 21.022
2
MTR014 Motor Neuron Disease 49 17.165
3
P LTR001 Lateral Sclerosis 46 17.165
4
FTD003 Ftdals1 33 15.669
5
c TRD001 Tardbp-Related Amyotrophic Lateral Sclerosis 13 15.669
6
PCK002 Pick Disease 61 14.015
7
c CNT035 Central Nervous System Disease 52 14.015
8
c AMY019 Amyotrophic Lateral Sclerosis Type 10 32 14.015
9
AMY040 Amyotrophic Lateral Sclerosis 10, with or Without Ftd 27 14.015
10
P ALZ034 Alzheimer Disease 98 12.137
11
CYS001 Cystic Fibrosis 90 12.137
12
HV1006 Hiv-1 77 12.137
13
INC002 Inclusion Body Myositis 67 12.137
14
P DMN033 Dementia, Frontotemporal 59 12.137
15
DMN002 Dementia 53 12.137
16
P NRV007 Nervous System Disease 49 12.137
17
SPC010 Speech and Communication Disorders 31 12.137
18
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 48 9.910
19
PRR007 Perry Syndrome 47 9.910
20
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 42 9.910
21
c AMY085 Amyotrophic Lateral Sclerosis 9 40 9.910
22
P CRT033 Corticobasal Degeneration 40 9.910
23
P PRS013 Prosopagnosia 38 9.910
24
SMN008 Semantic Dementia 37 9.910
25
ALX001 Alexia 36 9.910
26
P NRL007 Neurologic Diseases 35 9.910
27
c AMY083 Amyotrophic Lateral Sclerosis 11 35 9.910
28
c AMY023 Amyotrophic Lateral Sclerosis Type 6 35 9.910
29
IDM001 Ideomotor Apraxia 34 9.910
30
c AMY069 Amyotrophic Lateral Sclerosis 21 34 9.910
31
c AMY067 Amyotrophic Lateral Sclerosis 18 34 9.910
32
ADL060 Adult Polyglucosan Body Disease 33 9.910
33
ARG005 Argyrophilic Grain Disease 33 9.910
34
AGR018 Agraphia 33 9.910
35
c PRG001 Progressive Muscular Atrophy 33 9.910
36
BSL008 Basal Ganglia Disease 32 9.910
37
BRW001 Brown-Vialetto-Van Laere Syndrome 31 9.910
38
ANT007 Anterior Horn Cell Disease 30 9.910
39
NMN001 Nominal Aphasia 29 9.910
40
c AMY089 Amyotrophic Lateral Sclerosis 7 29 9.910
41
PST027 Postencephalitic Parkinson Disease 28 9.910
42
c AMY074 Amyotrophic Lateral Sclerosis Type 14 28 9.910
43
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 23 9.910
44
EXP001 Expressive Language Disorder 22 9.910
45
ASS001 Associative Agnosia 19 9.910
46
PHN002 Phonagnosia 18 9.910
47
DMN031 Dementia, Lewy Body 53 7.007
48
c TRD005 Tardbp-Related Frontotemporal Dementia 7 7.007