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ENPorphyria Cutanea Tarda (FPCT)
Alias:
Hepatoerythropoietic Porphyria
Hep
Uroporphyrinogen Decarboxylase Deficiency
Familial Porphyria Cutanea Tarda
Pct
Porphyria, Hepatocutaneous Type
Porphyria, Hepatoerythropoietic
Urod Deficiency
Heterozygous Uroporphyrinogen Decarboxylase Deficiency
Urod - [uroporphyrinogen Decarboxylase] Deficiency
Urod-Related Hepatoerythropoietic Porphyria
Porphyria Cutanea Tarda, Type Ii
Porphyria Cutanea Tarda Type Ii
Pct - [porphyria Cutanea Tarda]
Porphyria Hepatocutaneous Type
Pct, 'familial' Type
Pct, Type Ii
Pct Type Ii
Fpct
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Porphyria Cutanea Tarda, also known as hepatoerythropoietic porphyria, is related to porphyria cutanea tarda, type i and familial porphyria cutanea tarda. An important gene associated with Porphyria Cutanea Tarda is UROD (Uroporphyrinogen Decarboxylase), and among its related pathways/superpathways are Metabolism and Insulin receptor recycling. The drugs Deferasirox and Iron have been mentioned in the context of this disorder. Affiliated tissues include skin and liver, and related phenotypes are cutaneous photosensitivity and abnormal blistering of the skin
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MALACARDS
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