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Statements

Subject Item
dbr:Long-chain_3-hydroxyacyl-coenzyme_A_dehydrogenase_deficiency
rdf:type
yago:Illness114061805 owl:Thing yago:Abstraction100002137 yago:WikicatAutosomalRecessiveDisorders yago:IllHealth114052046 dbo:Disease yago:WikicatMetabolicDisorders yago:PhysicalCondition114034177 yago:Condition113920835 yago:State100024720 yago:GeneticDisease114151139 yago:Disorder114052403 yago:WikicatGeneticDisorders yago:MetabolicDisorder114084502 yago:PathologicalState114051917 wikidata:Q12136 umbel-rc:AilmentCondition yago:Disease114070360 yago:Attribute100024264 yago:WikicatFatty-acidMetabolismDisorders
rdfs:label
Déficit en 3-hydroxyacyl-coenzyme A déshydrogénase des acides gras à chaîne longue Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
rdfs:comment
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats into energy. This can become life-threatening, particularly during periods of fasting. Le déficit en 3-hydroxyacyl-coenzyme A déshydrogénase des acides gras à chaîne longue, souvent abrégé en déficit en LCHAD, est l'une des maladies rares à transmission autosomique récessive lié à l'oxydation des acides gras qui empêche le corps de convertir certaines graisses en énergie. Cela peut être dangereux, en particulier pendant les périodes de jeûne.
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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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Long-chain 3-hydroxyacyl-coenzyme; A dehydrogenase deficiency has an autosomal recessive pattern of inheritance.
dbp:synonyms
LCHAD deficiency
dbo:abstract
Le déficit en 3-hydroxyacyl-coenzyme A déshydrogénase des acides gras à chaîne longue, souvent abrégé en déficit en LCHAD, est l'une des maladies rares à transmission autosomique récessive lié à l'oxydation des acides gras qui empêche le corps de convertir certaines graisses en énergie. Cela peut être dangereux, en particulier pendant les périodes de jeûne. Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats into energy. This can become life-threatening, particularly during periods of fasting.
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