Search results for "[genes] SQSTM1"

30 hits were found for '[genes] SQSTM1'

# Family MCID Name MIFTS Score
1
PGT001 Paget's Disease of Bone 59 21.063
2
PGT007 Paget Disease of Bone 3 25 21.063
3
P HPT023 Hepatocellular Carcinoma 92 18.241
4
INC002 Inclusion Body Myositis 66 18.241
5
DMN002 Dementia 65 18.241
6
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 24 18.241
7
P ALZ034 Alzheimer Disease 92 16.651
8
c AMY091 Amyotrophic Lateral Sclerosis 1 78 16.651
9
MLT021 Multiple System Atrophy 70 16.651
10
MTR014 Motor Neuron Disease 58 16.651
11
PCK002 Pick Disease 68 14.893
12
P DMN033 Dementia, Frontotemporal 62 14.893
13
NNL002 Nonalcoholic Steatohepatitis 50 14.893
14
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 14.893
15
PRS037 Periostitis 30 14.893
16
P HNT016 Huntington Disease 80 12.898
17
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 12.898
18
P LTR001 Lateral Sclerosis 53 12.898
19
MYC013 Mycobacterium Abscessus 41 12.898
20
BSL008 Basal Ganglia Disease 40 12.898
21
OST079 Osteolysis, Familial Expansile 39 12.898
22
BHV002 Behavioral Variant of Frontotemporal Dementia 39 12.898
23
c AMY088 Amyotrophic Lateral Sclerosis 3 31 12.898
24
NNK001 Nonaka Myopathy 31 12.898
25
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 20 12.898
26
c SQS001 Sqstm1-Related Amyotrophic Lateral Sclerosis 10 12.898
27
P PLC011 Pilocytic Astrocytoma 60 10.531
28
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 39 10.531
29
c SPS126 Spastic Paraplegia 49, Autosomal Recessive 36 10.531
30
c GNR020 Gne-Related Myopathy 15 10.531