Iron-refractory iron deficiency anemia
Prevalence estimates on Rare Medical Network websites are calculated based on data available from numerous sources, including US and European government statistics, the NIH, Orphanet, and published epidemiologic studies. Rare disease population data is recognized to be highly variable, and based on a wide variety of source data and methodologies, so the prevalence data on this site should be assumed to be estimated and cannot be considered to be absolutely correct.
Age of Onset
Autosomal dominant ?A pathogenic variant in only one gene copy in each cell is sufficient to cause an autosomal dominant disease
Autosomal recessive ?Pathogenic variants in both copies of each gene of the chromosome are needed to cause an autosomal recessive disease and observe the mutant phenotype
X-linked dominant ?X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
X-linked recessive ?Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder
Mitochondrial or multigenic ?Mitochondrial genetic disorders can be caused by changes (mutations) in either the mitochondrial DNA or nuclear DNA that lead to dysfunction of the mitochondria and inadequate production of energy.
Multigenic or multifactor ?Inheritance involving many factors, of which at least one is genetic but none is of overwhelming importance, as in the causation of a disease by multiple genetic and environmental factors.
Other Names (AKA)
IRIDA; IRIDA syndrome; Anemia, hypochromic microcytic, with defect in iron metabolism;
Blood Diseases; Congenital and Genetic Diseases
Iron-refractory iron deficiency
IRIDA is caused by changes or
This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
|Medical Terms||Other Names||
|80%-99% of people have these symptoms|
|Abnormal intestine morphology||
Abnormality of the intestine
Mental retardation, nonspecific
[ more ]
|30%-79% of people have these symptoms|
|Decreased circulating copper concentration||
|Percent of people who have these symptoms is not available through HPO|
Unequal size of red blood cells
|Elevated hepcidin level||0031877|
Making a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional.
- The Genetic Testing Registry (GTR) provides information about the genetic tests for this condition. The intended audience for the GTR is health care providers and researchers. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.
- Orphanet lists international laboratories offering diagnostic testing for this condition.
Current treatment guidelines recommend an initial trial of oral iron along with vitamin C for several weeks to see if the anemia improves. If there is no improvement or minimal improvement, further treatment involves intravenous (IV) iron therapy. Even with IV therapy, only a partial improvement is expected. However in most cases, partial improvement of mild to moderate anemia results in enough healthy
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
- Genetics Home Reference (GHR) contains information on Iron-refractory iron deficiency anemia. This website is maintained by the National Library of Medicine.
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Iron-refractory iron deficiency anemia. Click on the link to view a sample search on this topic.
- Iron-refractory iron deficiency anemia. Genetics Home Reference (GHR). July, 2014; https://ghr.nlm.nih.gov/condition/iron-refractory-iron-deficiency-anemia.
- Sanchez Fernandez M. IRIDA syndrome. Orphanet. May, 2013; https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=209981.
- Bhatia P, Jain R, Singh A. A structured approach to iron refractory iron deficiency anemia (IRIDA) diagnosis (SAID): The more is “SAID” about iron, the less it is. Pediatric Hematology Oncology Journal. August, 2017; 2(2):48-53. https://www.sciencedirect.com/science/article/pii/S2468124517301055.
- Keskin EY and Yenicesu I. Iron-Refractory Iron Deficiency Anemia. Turk J Haematol. March, 2015; 32(1):1-14. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439901/.