Search results for "[genes] C9orf72"

26 hits were found for '[genes] C9orf72'

# Family MCID Name MIFTS Score
1
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 41 20.026
2
DMN002 Dementia 64 16.925
3
P LTR001 Lateral Sclerosis 52 16.925
4
c AMY091 Amyotrophic Lateral Sclerosis 1 78 15.138
5
APH002 Aphasia 53 13.110
6
APR001 Apraxia 48 13.110
7
SPC010 Speech and Communication Disorders 46 13.110
8
GNG005 Gangliocytoma 41 13.110
9
BHV002 Behavioral Variant of Frontotemporal Dementia 38 13.110
10
c C9R002 C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia 10 13.110
11
P DMN033 Dementia, Frontotemporal 63 10.704
12
MTR014 Motor Neuron Disease 59 10.704
13
PRR007 Perry Syndrome 57 10.704
14
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 10.704
15
c SPN304 Spinocerebellar Ataxia 8 50 10.704
16
NSH001 Nasu-Hakola Disease 45 10.704
17
BSL008 Basal Ganglia Disease 43 10.704
18
c PRG001 Progressive Muscular Atrophy 40 10.704
19
c AMY069 Amyotrophic Lateral Sclerosis 21 40 10.704
20
c AMY067 Amyotrophic Lateral Sclerosis 18 39 10.704
21
NMN001 Nominal Aphasia 33 10.704
22
BRW001 Brown-Vialetto-Van Laere Syndrome 29 10.704
23
P NRV007 Nervous System Disease 71 7.569
24
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 60 7.569
25
SMN008 Semantic Dementia 44 7.569
26
c HNT014 Huntington Disease-Like Syndrome Due to C9orf72 Expansions 9 7.569