Search results for "[genes] SQSTM1"

26 hits were found for '[genes] SQSTM1'

# Family MCID Name MIFTS Score
1
PGT001 Paget's Disease of Bone 55 22.823
2
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 39 20.128
3
PGT007 Paget Disease of Bone 3 25 20.128
4
DMN002 Dementia 51 18.635
5
HPT023 Hepatocellular Carcinoma 87 17.011
6
P ALZ034 Alzheimer Disease 91 15.215
7
P HNT016 Huntington Disease 67 15.215
8
MLT021 Multiple System Atrophy 64 15.215
9
MTR014 Motor Neuron Disease 48 15.215
10
c AMY091 Amyotrophic Lateral Sclerosis 1 74 13.177
11
INC002 Inclusion Body Myositis 63 13.177
12
PCK002 Pick Disease 58 13.177
13
P DMN033 Dementia, Frontotemporal 57 13.177
14
P LTR001 Lateral Sclerosis 45 13.177
15
NNL002 Nonalcoholic Steatohepatitis 45 13.177
16
c AMY088 Amyotrophic Lateral Sclerosis 3 27 13.177
17
P PRK057 Parkinson Disease, Late-Onset 69 10.759
18
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 47 10.759
19
MCL002 Macular Corneal Dystrophy 47 10.759
20
OST079 Osteolysis, Familial Expansile 40 10.759
21
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 36 10.759
22
MYC013 Mycobacterium Abscessus 35 10.759
23
FTD003 Ftdals1 23 10.759
24
P LYN001 Lynch Syndrome 69 7.608
25
P PLC011 Pilocytic Astrocytoma 52 7.608
26
BHV002 Behavioral Variant of Frontotemporal Dementia 27 7.608