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Hemochromatosis, type 3 MeSH Supplementary Concept Data 2024


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 Number
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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