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Disease Info Card
Porphobilinogen Synthase Deficiency
Information about Porphobilinogen Synthase Deficiency: 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 Porphobilinogen Synthase Deficiency
Most recent studies have shown that Porphobilinogen Synthase Deficiency shares some biological mechanisms with abdominal-pain, acute-intermittent-porphyria, acute-interstitial-pneumonia, anemia, carcinoma, disorders-of-porphyrin-metabolism, erythropoietic-protoporphyria, hereditary-coproporphyria, hypertensive-disease, lead-poisoning, liver-carcinoma, liver-diseases, metabolic-diseases, pain, poisoning, porphyria-cutanea-tarda, porphyria-erythropoietic, porphyrias-hepatic, variegate-porphyria.
Among the many pathways, these few ones have gauged particular interests from scientists studying Porphobilinogen Synthase Deficiency, and have been seen in publications frequently: Excretion, Pathogenesis, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Porphobilinogen Synthase Deficiency, such as AIP, ALAD, AMBP, AURKAIP1, AVP, CAT, CPO, CPOX, CRAT, DDC, FECH, GLYAT, HCRT, HMBS, HRC, PPOX, PTPN6, TDO2, 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 Porphobilinogen Synthase Deficiency
This information is being compiled and will come in a future update
| Excretion | Pathogenesis | Secretion |
| Translation | Transport |