Carnitine palmitoyltransferase I deficiency is a rare metabolic disorder that prevents the body from converting certain fats called long-chain fatty acids into energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme that prevents these long-chain fatty acids from being transported into the mitochondria to be broken down.

PropertyValue
dbpedia-owl:Disease/diseasesdb
  • 32535
dbpedia-owl:Disease/emedicineSubject
  • ped
dbpedia-owl:Disease/emedicineTopic
  • 321
dbpedia-owl:Disease/omim
  • 255120
dbpedia-owl:diseasesdb
  • 32535
dbpedia-owl:emedicineSubject
  • ped
dbpedia-owl:emedicineTopic
  • 321
dbpedia-owl:omim
  • 255120
dbpedia-owl:thumbnail
dbpprop:abstract
  • Carnitine palmitoyltransferase I deficiency is a rare metabolic disorder that prevents the body from converting certain fats called long-chain fatty acids into energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme that prevents these long-chain fatty acids from being transported into the mitochondria to be broken down.
dbpprop:caption
dbpprop:diseasesdb
  • 32535 (xsd:integer)
dbpprop:emedicinesubj
  • ped
dbpprop:emedicinetopic
  • 321 (xsd:integer)
dbpprop:hasPhotoCollection
dbpprop:image
  • Carnitine structure.png
dbpprop:name
  • Carnitine palmitoyltransferase I deficiency
dbpprop:omim
  • 255120 (xsd:integer)
dbpprop:reference
dbpprop:wikiPageUsesTemplate
dbpprop:wordnet_type
rdf:type
rdfs:comment
  • Carnitine palmitoyltransferase I deficiency is a rare metabolic disorder that prevents the body from converting certain fats called long-chain fatty acids into energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme that prevents these long-chain fatty acids from being transported into the mitochondria to be broken down.
rdfs:label
  • Carnitine palmitoyltransferase I deficiency
owl:sameAs
skos:subject
foaf:depiction
foaf:name
  • Carnitine palmitoyltransferase I deficiency
foaf:page
is dbpprop:redirect of
is owl:sameAs of