About: inborn disorder of fatty acid oxidation and ketone body metabolism

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About: inborn disorder of fatty acid oxidation and ketone body metabolism Goto Sponge NotDistinct Permalink

An Entity of Type : http://wikiba.se/ontology#Item, within Data Space : covidontheweb.inria.fr associated with source document(s)

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type	Item
label	inborn disorder of fatty acid oxidation and ketone body metabolism
preferred label	inborn disorder of fatty acid oxidation and ketone body metabolism
described by	https://covidontheweb.inria.fr:4443/about/id/entity/http/ns.inria.fr/covid19/graph/wikidata-named-entities-full proxy:entity/http/ns.inria.fr/covid19/graph/wikidata-named-entities-full https://covidontheweb.inria.fr:4443/about/id/entity/http/www.wikidata.org/entity/Q55787301
schema:name	inborn disorder of fatty acid oxidation and ketone body metabolism
schema:description	human disease
is wdt:P279 of	disorder of fatty acid oxidation and ketogenesis long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency medium chain acyl-CoA dehydrogenase deficiency Systemic primary carnitine deficiency very long chain acyl-CoA dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency 3-hydroxyacyl-coenzyme A dehydrogenase deficiency multiple acyl-CoA dehydrogenase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Succinyl-CoA:3-oxoacid CoA transferase deficiency carnitine-acylcarnitine translocase deficiency beta-ketothiolase deficiency short-chain acyl-coenzyme A dehydrogenase deficiency
is topic of	disorder of fatty acid oxidation and ketogenesis covid:graph/wikidata-named-entities-full
is http://www.wikidat...op/statement/P279 of	wd:statement/Q55787301-DA40B686-2BA0-416C-85FF-824E96945DC9

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