Hemochromatosis, Type 2B MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Hemochromatosis, Type 2B
Unique ID: C566557
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566557
Registry Number: 0
Heading Mapped to: Hemochromatosis / *congenital
Frequency: 0
Note: mutation in HAMP
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Hemochromatosis, Type 2B Preferred

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