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bn:03350107n
Noun Concept
Categories: Rare diseases, Amino acid metabolism disorders, Articles with short description, Fatty-acid metabolism disorders, Autosomal recessive disorders
EN
propionic acidemia  Acidemia, propionic  glycinemia, ketotic  Hyperglycinemia With Ketoacidosis and Leukopenia  ketotic glycinemia  PROP
EN
Propionic acidemia, also known as propionic aciduria or propionyl-CoA carboxylase deficiency, is a rare autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia. Wikipedia
Definitions
Relations
Sources
EN
Propionic acidemia, also known as propionic aciduria or propionyl-CoA carboxylase deficiency, is a rare autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia. Wikipedia
Organic acidemia that involes a nonfunctional propionyl CoA carboxylase affecting conversion of aminio acids and fats into sugar for energy Wikidata
IS A
rare disease
organic acidemia
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
propionic acidemia
Wikidata
EN
propionic acidemia
Wikipedia Redirections
EN
Acidemia, propionic, Ketotic glycinemia, propionic aciduria, propionyl-CoA carboxylase deficiency
Wikidata Alias
EN
glycinemia, ketotic, Hyperglycinemia With Ketoacidosis and Leukopenia, ketotic glycinemia, ketotic hyperglycinemia, ketotic II glycinemia, Pcc Deficiency, PROP, PROPIONIC ACIDEMIA, propionic aciduria, Propionicacidemia, propionyl-CoA carboxylase deficiency

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