MeSH Browser

MeSH Supplementary: Hemochromatosis, type 4
Unique ID: C537249
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537249
Entry Term(s): Hemochromatosis due to defect in ferroportin; Hemochromatosis, autosomal dominant
Registry Number: 0
Heading Mapped to: *Hemochromatosis; Cation Transport Proteins / *deficiency
Frequency: 18
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Hemochromatosis, type 4 MeSH Supplementary Concept Data 2024