Diamond-Blackfan anemia 13

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Disease Overview

Any Diamond-Blackfan anemia in which the cause of the disease is a mutation in the RPS29 gene.

Synonyms

DBA13
Diamond-Blackfan Anaemia type 13
Diamond-Blackfan Anemia type 13
Diamond-Blackfan anaemia caused by mutation in RPS29
Diamond-Blackfan anemia 13
Diamond-Blackfan anemia caused by mutation in RPS29
RPS29 Diamond-Blackfan anaemia
RPS29 Diamond-Blackfan anemia

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.