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Concept information

Clinical finding (finding) > disease > Metabolic disease > Mitochondrial myopathy > Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)
... > Clinical finding (finding) > disease > Metabolic disease > Neonatal metabolic disorder (disorder) > Neonatal acidosis (disorder) > Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)
... > Clinical finding (finding) > Newborn finding > Neonatal disease > Neonatal metabolic disorder (disorder) > Neonatal acidosis (disorder) > Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of acid-base balance > Acidosis > Neonatal acidosis (disorder) > Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)

Preferred term

Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)  

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  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/773423007

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