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About: Inborn error of lipid metabolism     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : umbel-rc:AilmentCondition, within Data Space : dbpedia.demo.openlinksw.com associated with source document(s)

Type: ThingDiseaseyago:WikicatLipidMetabolismDisordersyago:Abstraction100002137yago:Acid114607521yago:Attribute100024264yago:CarboxylicAcid114739360yago:Chemical114806838yago:Compound114818238yago:Condition113920835yago:Disease114070360yago:Disorder114052403yago:FattyAcid114740227yago:IllHealth114052046yago:Illness114061805yago:Material114580897yago:Matter100020827yago:Part113809207yago:PathologicalState114051917yago:PhysicalCondition114034177yago:PhysicalEntity100001930yago:Relation100031921diseaseyago:State100024720yago:Substance100019613yago:WikicatFattyAcidsumbel-rc:AilmentCondition New Facet based on Instances of this Class

Numerous genetic disorders are caused by errors in fatty acid metabolism. These disorders may be described as fatty oxidation disorders or as a lipid storage disorders, and are any one of several inborn errors of metabolism that result from enzyme defects affecting the ability of the body to oxidize fatty acids in order to produce energy within muscles, liver, and other cell types. Some of the more common fatty acid metabolism disorders are: