Search results for "[genes] SQSTM1"

28 hits were found for '[genes] SQSTM1'

# Family MCID Name MIFTS Score
1
PGT001 Paget's Disease of Bone 57 22.596
2
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 27 19.928
3
DMN002 Dementia 53 18.449
4
HPT023 Hepatocellular Carcinoma 90 16.842
5
c AMY091 Amyotrophic Lateral Sclerosis 1 83 16.842
6
P ALZ034 Alzheimer Disease 98 15.064
7
MLT021 Multiple System Atrophy 63 15.064
8
MTR014 Motor Neuron Disease 49 15.064
9
FTD003 Ftdals1 33 15.064
10
PGT007 Paget Disease of Bone 3 22 15.064
11
P HNT016 Huntington Disease 78 13.046
12
INC002 Inclusion Body Myositis 67 13.046
13
PCK002 Pick Disease 61 13.046
14
P DMN033 Dementia, Frontotemporal 59 13.046
15
P LTR001 Lateral Sclerosis 46 13.046
16
HYP068 Hyperostosis 45 13.046
17
NNL002 Nonalcoholic Steatohepatitis 43 13.046
18
PRS037 Periostitis 32 13.046
19
BNR001 Bone Remodeling Disease 28 13.046
20
BHV002 Behavioral Variant of Frontotemporal Dementia 26 13.046
21
c AMY088 Amyotrophic Lateral Sclerosis 3 26 13.046
22
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 48 10.652
23
P PLC011 Pilocytic Astrocytoma 42 10.652
24
OST079 Osteolysis, Familial Expansile 39 10.652
25
MYC013 Mycobacterium Abscessus 35 10.652
26
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 23 10.652
27
PGT009 Paget Disease of Bone 2, Early-Onset 25 7.532
28
PGT002 Paget Disease of Bone, Familial 8 7.532