About: Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

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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.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:WikicatMetabolicDisorders yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Disease114070360 yago:Disorder114052403 yago:GeneticDisease114151139 yago:IllHealth114052046 yago:Illness114061805 yago:MetabolicDisorder114084502 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:WikicatGeneticDisorders disease yago:State100024720 yago:WikicatFatty-acidMetabolismDisorders umbel-rc:AilmentCondition
rdfs:label	Déficit en 3-hydroxyacyl-coenzyme A déshydrogénase des acides gras à chaîne longue (fr) Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (en)
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. (en) 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. (fr)
foaf:name	Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (en)
name	Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (en)
foaf:depiction
dcterms:subject	Autosomal recessive disorders Fatty-acid metabolism disorders
Wikipage page ID	1557100 (xsd:integer)
Wikipage revision ID	1084520391 (xsd:integer)
Link from a Wikipage to another Wikipage	Mutation Nervous system Hypoglycemia Peripheral neuropathy Retina Lethargy Coma Coenzyme A Enzyme Autosomal recessive disorders Liver Fatty acid Fatty acid metabolism Autosomal recessive HADHA Lipid Fasting Fatty-acid metabolism disorders Heart Hypotonia Mitochondrial trifunctional protein Virus Fatty acid oxidation disorder Medium chain acyl dehydrogenase deficiency
sameAs	Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Empty_section dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Refimprove dbt:Reflist dbt:Medicine dbt:Fatty-acid_metabolism_disorders
thumbnail	wiki-commons:Special:FilePath/autorecessive.svg?width=300
ICD	277.850000 (xsd:double) (en)
OMIM	600890 (xsd:integer)
caption	Long-chain 3-hydroxyacyl-coenzyme; A dehydrogenase deficiency has an autosomal recessive pattern of inheritance. (en)
synonyms	LCHAD deficiency (en)
has abstract	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. (en) 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. (fr)
eMedicineSubj	ped (en)
eMedicineTopic	1284 (xsd:integer)
gold:hypernym	Disorder
dbp:wordnet_type	http://www.w3.org/2006/03/wn/wn20/instances/synset-disease-noun-1
ICD9	277.85
eMedicine subject	ped (en)
eMedicine topic	1284 (en)
prov:wasDerivedFrom	wikipedia-en:Long-chain_3-hydroxyacyl-coenzyme_A_dehydrogenase_deficiency?oldid=1084520391&ns=0
page length (characters) of wiki page	4163 (xsd:nonNegativeInteger)
OMIM id	600890 (xsd:integer)
foaf:isPrimaryTopicOf	wikipedia-en:Long-chain_3-hydroxyacyl-coenzyme_A_dehydrogenase_deficiency
is Link from a Wikipage to another Wikipage of	Rhabdomyolysis Inborn error of lipid metabolism List of neuromuscular disorders Fatty-acid metabolism disorder Acute fatty liver of pregnancy HADHA Chromosome 2

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