Search results for "[genes] SQSTM1"

26 hits were found for '[genes] SQSTM1'

# Family MCID Name MIFTS Score
1
PGT001 Paget's Disease of Bone 64 22.823
2
PGT007 Paget Disease of Bone 3 32 20.128
3
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 25 20.128
4
DMN002 Dementia 64 18.635
5
HPT023 Hepatocellular Carcinoma 90 17.011
6
P ALZ034 Alzheimer Disease 94 15.215
7
MLT021 Multiple System Atrophy 71 15.215
8
P HNT016 Huntington Disease 71 15.215
9
MTR014 Motor Neuron Disease 61 15.215
10
c AMY091 Amyotrophic Lateral Sclerosis 1 79 13.177
11
PCK002 Pick Disease 65 13.177
12
INC002 Inclusion Body Myositis 65 13.177
13
P DMN033 Dementia, Frontotemporal 62 13.177
14
P LTR001 Lateral Sclerosis 56 13.177
15
NNL002 Nonalcoholic Steatohepatitis 55 13.177
16
c AMY088 Amyotrophic Lateral Sclerosis 3 35 13.177
17
P PRK057 Parkinson Disease, Late-Onset 74 10.759
18
MCL002 Macular Corneal Dystrophy 54 10.759
19
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 51 10.759
20
OST079 Osteolysis, Familial Expansile 39 10.759
21
MYC013 Mycobacterium Abscessus 38 10.759
22
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 33 10.759
23
FTD003 Ftdals1 30 10.759
24
P LYN001 Lynch Syndrome 71 7.608
25
P PLC011 Pilocytic Astrocytoma 63 7.608
26
BHV002 Behavioral Variant of Frontotemporal Dementia 32 7.608