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About: Porphyria cutanea tarda     Goto   Sponge   NotDistinct   Permalink

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

Type: ThingFuchs' dystrophyyago:WikicatAutosomalDominantDisordersyago:WikicatCutaneousConditionsyago:WikicatMetabolicDisordersyago:WikicatSkinConditionsResultingFromErrorsInMetabolismyago:Abstraction100002137yago:Attribute100024264yago:AutosomalDominantDisease114162025yago:Condition113920835yago:Disease114070360yago:Disorder114052403yago:GeneticDisease114151139yago:IllHealth114052046yago:Illness114061805yago:MetabolicDisorder114084502yago:PathologicalState114051917yago:PhysicalCondition114034177yago:Porphyria114507651yago:WikicatGeneticDisordersdiseaseyago:State100024720yago:WikicatPorphyriasumbel-rc:AilmentCondition New Facet based on Instances of this Class

Porphyria cutanea tarda is the most common subtype of porphyria. The disease is named because it is a porphyria that often presents with skin manifestations later in life. The disorder results from low levels of the enzyme responsible for the fifth step in heme production. Heme is a vital molecule for all of the body's organs. It is a component of hemoglobin, the molecule that carries oxygen in the blood. Hepatoerythropoietic porphyria has been described as a homozygous form of porphyria cutanea tarda, although it can also be caused if two different mutations occur at the same locus.