MeSH Browser

MeSH Supplementary: Diamond-Blackfan Anemia 1
Unique ID: C567302
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567302
Registry Numbers: 0
Heading Mapped to: *Anemia, Diamond-Blackfan
Frequency: 11
Note: A type of Diamond-Blackfan Anemia. Patients may also have craniofacial, skeletal, and cardiovascular abnormalities. It is caused by mutations in the ribosomal protein S19 (RPS19) gene. OMIM: 105650
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Diamond-Blackfan Anemia 1 MeSH Supplementary Concept Data 2025