Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 Biomarker disease BEFREE In AARS2 leukodystrophy cases reported thus far, there is nearly invariable progression to severe disability and atrophy of involved brain regions, often within a decade. 31839000 2019
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE Our data provide further evidence that mutations of AARS2 are implicated in adult-onset leukodystrophy. 31106991 2019
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE Our findings have important implications on genetic counseling for any case with leukodystrophy and extend the mutational spectrum in AARS2 gene. 31388113 2019
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 Biomarker disease BEFREE These cases expand the clinical heterogeneity of AARS2-related disorders, given that the first and third case represent some of the oldest known survivors of this disease, the second is adult-onset AARS2-related neurological decline without leukodystrophy, and the third is biallelic AARS2-related disorder involving a partial gene deletion. 31099476 2019
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE Recently, also autosomal recessive mutations in AARS2 gene were found to be the cause of an adult-onset leukodystrophy with axonal spheroids. 29749055 2018
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE Alanyl-tRNA synthetase 2 (AARS2) pathogenic variants have been reported to cause leukodystrophy with ovarian failure, and cardiomyopathy (#615889) as well as combined oxidative phosphorylation deficiency-8 (#614096). 28820624 2018
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE The diagnosis of AARS2 gene mutations causing leukodystrophy was confirmed by genetic testing. 27734837 2017
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE The first Japanese case of leukodystrophy with ovarian failure arising from novel compound heterozygous AARS2 mutations. 27251004 2016
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.090 GeneticVariation disease BEFREE Novel (ovario) leukodystrophy related to AARS2 mutations. 24808023 2014