6.2.1.4 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18392745&form=6&db=m Disorders caused by deficiency of succinate-CoA ligase. causal interaction,unassigned 4,0 6.2.1.4 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20227526&form=6&db=m Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch. causal interaction,unassigned 4,0 6.2.1.4 Acidosis, Lactic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19526370&form=6&db=m A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria. causal interaction,unassigned 3,0 6.2.1.4 Acidosis, Lactic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21093335&form=6&db=m Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder. causal interaction,ongoing research,unassigned 4,2,0 6.2.1.4 Acidosis, Lactic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21639866&form=6&db=m Neonatal lactic acidosis with methylmalonic aciduria by novel mutations in the SUCLG1 gene. causal interaction,unassigned 4,0 6.2.1.4 Adenocarcinoma, Mucinous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34174878&form=6&db=m Multi-omics analyses of human colorectal cancer revealed three mitochondrial genes potentially associated with poor outcomes of patients. unassigned - 6.2.1.4 Adenoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28709933&form=6&db=m Identification of novel biomarker and therapeutic target candidates for diagnosis and treatment of follicular carcinoma. diagnostic usage,therapeutic application,unassigned 3,1,0 6.2.1.4 Adenoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34174878&form=6&db=m Multi-omics analyses of human colorectal cancer revealed three mitochondrial genes potentially associated with poor outcomes of patients. unassigned - 6.2.1.4 Alzheimer Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25027320&form=6&db=m SUCLG2 identified as both a determinator of CSF A?1-42 levels and an attenuator of cognitive decline in Alzheimer's disease. causal interaction,unassigned 2,0 6.2.1.4 Anemia, Sideroblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10727444&form=6&db=m Interaction between succinyl CoA synthetase and the heme-biosynthetic enzyme ALAS-E is disrupted in sideroblastic anemia. causal interaction,unassigned 2,0