HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

Autosomal Dominant Iron Overload

Also Known As:

Iron Overload, Autosomal Dominant

Networked: 7 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Iron Metabolism Disorders: 78
    - Iron Overload: 7614
      - Autosomal Dominant Iron Overload: 7

Related Diseases

1.	Hemochromatosis (Bronze Diabetes)
2.	Fibrosis (Cirrhosis)

Experts

1.	Brissot, Pierre: 2 articles (11/2013 - 08/2003)
2.	David, Véronique: 2 articles (11/2013 - 08/2003)
3.	Jouanolle, Anne-Marie: 2 articles (11/2013 - 08/2003)
4.	Loréal, Olivier: 2 articles (11/2013 - 08/2003)
5.	Bonaccorsi di Patti, Maria Carmela: 1 article (02/2018)
6.	Cortese, Andrea: 1 article (02/2018)
7.	De Bernardo, Carmelilia: 1 article (02/2018)
8.	De Muro, Marianna: 1 article (02/2018)
9.	Di Bartolomeo, Sabrina: 1 article (02/2018)
10.	Faienza, Fiorella: 1 article (02/2018)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Autosomal Dominant Iron Overload:

1.	IronIBA 04/01/2004 - "Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis." 02/01/2018 - "Mutations of SLC40A1 encoding ferroportin (Fpn), the unique cellular iron exporter, severely affect iron homeostasis causing type 4 hereditary hemochromatosis, an autosomal dominant iron overload condition with variable phenotypic manifestations. " 09/21/2007 - "An adult onset form of HH similar to HFE-HH is caused by homozygosity for mutations in transferrin receptor 2. The autosomal dominant iron overload disorder ferroportin disease is caused by mutations in the iron exporter ferroportin. " 07/01/2001 - "A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload."
2.	metal transporting protein 1 (ferroportin)IBA 01/01/2006 - "This report describes the clinical and laboratory findings of two Spanish families with autosomal dominant iron overload associated with previously unrecognized Ferroportin 1 mutations (p.R88T and p.I180T). " 08/01/2003 - "Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload." 02/01/2018 - "Mutations of SLC40A1 encoding ferroportin (Fpn), the unique cellular iron exporter, severely affect iron homeostasis causing type 4 hereditary hemochromatosis, an autosomal dominant iron overload condition with variable phenotypic manifestations. " 09/21/2007 - "An adult onset form of HH similar to HFE-HH is caused by homozygosity for mutations in transferrin receptor 2. The autosomal dominant iron overload disorder ferroportin disease is caused by mutations in the iron exporter ferroportin. "
3.	Transferrin (beta 2 Transferrin)IBA 11/01/2013 - "Mutations in the FPN gene (SLC40A1) lead to autosomal dominant iron overload diseases related either to loss or to gain of function, and usually characterized by normal or low transferrin saturation versus elevated transferrin saturation, respectively. "
4.	Messenger RNA (mRNA)IBA 07/01/2001 - "A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload."
5.	Transferrin Receptors (Transferrin Receptor)IBA 09/21/2007 - "An adult onset form of HH similar to HFE-HH is caused by homozygosity for mutations in transferrin receptor 2. The autosomal dominant iron overload disorder ferroportin disease is caused by mutations in the iron exporter ferroportin. "
6.	ElementsIBA 07/01/2001 - "A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload."
7.	ApoferritinsIBA 07/01/2001 - "A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload."