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SOD1 and Parkinson disease are reported together in 2 articles.

Gene

SOD1

HGNC
HGNC:11179
60articles
60mentions
3variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
280articles
280mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

2 records shown · first 60

Recent advances in stem cell therapy: efficacy, ethics, safety concerns, and future directions focusing on neurodegenerative disorders - a review.

PMID 39705668 | PMCID PMC11486982 | DOI 10.1097/JS9.0000000000001609 · International journal of surgery (London, England) · 2024 · 4 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneSOD1“Neurodegeneration refers to the gradual loss of neurons and extensive changes in glial cells like tau inclusions in astrocytes and oligodendrocytes, α-synuclein inclusions in oligodendrocytes and SOD1 aggregates in astrocytes along with deterioration in the motor, cognition, learning, and behavior.”0.98hgnc_dict_v1
phenotypeParkinson disease“Common neurodegenerative disorders are Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS), Huntington's disease (HD), spinocerebellar ataxia (SCA), and supranuclear palsy.”0.93phenotype_alias_lexicon_v2
phenotypeamyotrophic lateral sclerosis“Common neurodegenerative disorders are Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS), Huntington's disease (HD), spinocerebellar ataxia (SCA), and supranuclear palsy.”0.98phenotype_alias_lexicon_v2
phenotypeAlzheimer disease“Common neurodegenerative disorders are Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS), Huntington's disease (HD), spinocerebellar ataxia (SCA), and supranuclear palsy.”0.93phenotype_alias_lexicon_v2

The Role of Mitochondrial Genes in Neurodegenerative Disorders.

PMID 34503413 | PMCID PMC9881096 | DOI 10.2174/1570159X19666210908163839 · Current neuropharmacology · 2022 · 7 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneSOD1“These abnormalities, including PINK1, Parkin, and SOD1 mutations, seem to reveal mitochondrial dysfunctions due to either mtDNA mutation or deletion, the mechanism of which remains unclear in depth.”0.98hgnc_dict_v1
phenotypeParkinson disease“This review describes various gene mutations in Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, multiple sclerosis, and stroke.”0.93phenotype_alias_lexicon_v2
genePINK1“These abnormalities, including PINK1, Parkin, and SOD1 mutations, seem to reveal mitochondrial dysfunctions due to either mtDNA mutation or deletion, the mechanism of which remains unclear in depth.”0.98hgnc_dict_v1
phenotypestroke“This review describes various gene mutations in Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, multiple sclerosis, and stroke.”0.98phenotype_alias_lexicon_v2