Hemochromatosis, type 3 MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Hemochromatosis, type 3
Unique ID: C537248
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537248
Entry Term(s): Hemochromatosis due to defect in transferrin receptor 2
Registry Numbers: 0
Heading Mapped to: *Hemochromatosis; Receptors, Transferrin / deficiency
Frequency: 7
Note: Hemochromatosis due to defect in transferrin receptor 2
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Hemochromatosis, type 3 Preferred

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