Hereditary Coproporphyria

Overview of Hereditary Coproporphyria

Most recent studies have shown that Hereditary Coproporphyria shares some biological mechanisms with abdominal-pain, acute-intermittent-porphyria, acute-interstitial-pneumonia, dermatologic-disorders, disorders-of-porphyrin-metabolism, epilepsy, erythropoietic-protoporphyria, hepatoerythropoietic-porphyria, homozygous-hereditary-coproporphyria, hypertensive-disease, liver-diseases, metabolic-diseases, pain, photosensitivity-disorders, porphobilinogen-synthase-deficiency, porphyria-cutanea-tarda, porphyria-erythropoietic, porphyrias-hepatic, variegate-porphyria.

Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Coproporphyria, and have been seen in publications frequently: Coagulation, Excretion, Hormone Secretion, Keratinization, Localization, Oxygen Transport, Pathogenesis, Pigmentation, Secretion, Translation, Transport

Quite a number of genes have been found to play important roles in Hereditary Coproporphyria, such as AIP, ALAD, AMBP, ARNTL, AURKAIP1, AVP, CPO, CPOX, EBP, EPX, FECH, GATA1, HCRT, HMBS, HRC, PPOX, PTPN6, TBX22, 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.

Hereditary Coproporphyria Related Genes

click to see detail information for each gene

Pathways Related to Hereditary Coproporphyria

This information is being compiled and will come in a future update

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