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Disease Info Card
Familial Porphyria Cutanea Tarda
Information about Familial Porphyria Cutanea Tarda: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Familial Porphyria Cutanea Tarda
Most recent studies have shown that Familial Porphyria Cutanea Tarda shares some biological mechanisms with acute-intermittent-porphyria, de-novo-mutation, dermatologic-disorders, disorders-of-porphyrin-metabolism, erythropoietic-protoporphyria, hemochromatosis, hepatitis, hepatitis-c, hepatoerythropoietic-porphyria, hypertrichosis, hypokinesia, liver-diseases, porphyria-cutanea-tarda, porphyria-erythropoietic, porphyrias-hepatic, siderosis, uroporphyrinuria, virus-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Familial Porphyria Cutanea Tarda, and have been seen in publications frequently: Excretion, Pathogenesis, Translation, Transport
Quite a number of genes have been found to play important roles in Familial Porphyria Cutanea Tarda, such as ABCC1, ABCC4, ACTA1, ALAD, EPHB6, EPX, FECH, GSTK1, HFE, HMBS, HPSE, SLCO6A1, TNFSF14, UROD. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Familial Porphyria Cutanea Tarda
This information is being compiled and will come in a future update
| Excretion | Pathogenesis | Translation |
| Transport |