MeSH Browser

MeSH Supplementary: Hemoglobin M Disease
Unique ID: C581942
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C581942
Registry Number: 0
Heading Mapped to: Hemoglobin M; Methemoglobinemia / *congenital
Frequency: 10
Note: promote; specific types of Hemoglobin M disease (methemoglobinemia due to hemoglobin M beta types, or alpha types) represented by several scr
Date of Entry: 2013/11/06

Hemoglobin M Disease MeSH Supplementary Concept Data 2024