Disease Info Card

Disorders Of Porphyrin Metabolism

Information about Disorders Of Porphyrin Metabolism: 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 Disorders Of Porphyrin Metabolism

Most recent studies have shown that Disorders Of Porphyrin Metabolism shares some biological mechanisms with abdominal-pain, acute-intermittent-porphyria, acute-interstitial-pneumonia, anemia, bulla, dermatologic-disorders, erythropoietic-protoporphyria, hemochromatosis, hepatitis, hepatitis-c, lead-poisoning, liver-cirrhosis, liver-diseases, metabolic-diseases, pain, photosensitivity-disorders, porphyria-cutanea-tarda, porphyria-erythropoietic, porphyrias-hepatic, variegate-porphyria.

Among the many pathways, these few ones have gauged particular interests from scientists studying Disorders Of Porphyrin Metabolism, and have been seen in publications frequently: Aging, Cell Proliferation, Coagulation, Complement Activation, Conjugation, Cytolysis, Excretion, Gluconeogenesis, Hormone Secretion, Hypersensitivity, Localization, Ovulation, Oxidative Phosphorylation, Pathogenesis, Photoprotection, Pigmentation, Regeneration, Secretion, Translation, Transport

Quite a number of genes have been found to play important roles in Disorders Of Porphyrin Metabolism, such as AIP, ALAD, ALB, AURKAIP1, AVP, CAT, CPOX, EPO, EPX, FECH, HCRT, HFE, HMBS, PPOX, TDO2, TF, TNFSF14, UROD, UROS. 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.