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EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Acidosis
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
3
Acidosis
Disorders caused by deficiency of succinate-CoA ligase.
causal interaction
4
Acidosis
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch.
unassigned
0
Acidosis
Disorders caused by deficiency of succinate-CoA ligase.
unassigned
0
Acidosis, Lactic
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder.
causal interaction
3
Acidosis, Lactic
Neonatal lactic acidosis with methylmalonic aciduria by novel mutations in the SUCLG1 gene.
causal interaction
4
Acidosis, Lactic
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
causal interaction
2
Acidosis, Lactic
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder.
ongoing research
2
Acidosis, Lactic
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder.
unassigned
0
Acidosis, Lactic
Neonatal lactic acidosis with methylmalonic aciduria by novel mutations in the SUCLG1 gene.
unassigned
0
Results 1 - 10 of 90 > >>