MeSH Browser

MeSH Supplementary: Alpha-Thalassemia Myelodysplasia Syndrome
Unique ID: C563023
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563023
Entry Term(s): Hemoglobin H Disease, Acquired
Registry Numbers: 0
Heading Mapped to: *Myelodysplastic Syndromes; *alpha-Thalassemia; *Genetic Diseases, X-Linked
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Alpha-Thalassemia Myelodysplasia Syndrome MeSH Supplementary Concept Data 2025