Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 Biomarker group BEFREE Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report. 30352563 2018
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Mutations in some of these genes, including aspartyl-tRNA synthetase (DARS2), lead to the onset of a white matter disease-leukoencephalopathy with brainstem and spinal cord involvement, and lactate elevation (LBSL) characterized by progressive spastic ataxia and characteristic leukoencephalopathy signature with multiple long-tract involvements. 28985337 2017
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Here, we investigate six mutants of the aspartyl-tRNA synthetase correlated with leukoencephalopathies. 26620921 2015
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Early-onset leukoencephalopathy due to a homozygous missense mutation in the DARS2 gene. 26327357 2015
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Intriguingly, HBSL bears a striking resemblance to leukoencephalopathy with brain stem and spinal cord involvement and elevated lactate (LBSL), which is caused by mutations in the mitochondria-specific DARS2, suggesting that these two diseases might share a common underlying molecular pathology. 23643384 2013
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 Biomarker group BEFREE The autosomal recessive white matter disorder LBSL (leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation) is caused by mutations in DARS2, coding for mtAspRS (mitochondrial aspartyl-tRNA synthetase). 23216004 2013
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Neuropathology of leukoencephalopathy with brainstem and spinal cord involvement and high lactate caused by a homozygous mutation of DARS2. 22677571 2013
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a report of three adult patients. 23652419 2013
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 Biomarker group BEFREE LBSL (leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation) is an autosomal recessive white matter disorder with slowly progressive cerebellar ataxia, spasticity and dorsal column dysfunction. 22023289 2012
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Of interest, we found an intronic variant in DARS2, a gene involved in mitochondrial DNA translation, responsible for the syndrome of leukoencephalopathy with brainstem and spinal cord involvement and high brain lactate. 21427441 2011
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 GeneticVariation group BEFREE Mutations in the nuclear gene coding for the mitochondrial aspartyl-tRNA synthetase, a key enzyme for mitochondrial translation, are correlated with leukoencephalopathy. 21121901 2011
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.200 Biomarker group HPO