MeSH Browser

MeSH Supplementary: Congenital atransferrinemia
Unique ID: C538259
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538259
Entry Term(s): Atransferrinemia; Familial hypotransferrinemia; Hypotransferrinemia, Familial
Heading Mapped to: *Metal Metabolism, Inborn Errors; Transferrin / deficiency
Frequency: 8
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Concept UI: M0532720
Terms: Congenital atransferrinemia Preferred Term
Term UI T752953
Date06/18/2009
LexicalTag NON
ThesaurusID ORD (2010); Familial hypotransferrinemia
Term UI T745230
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Hypotransferrinemia, Familial
Term UI T807630
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Atransferrinemia
Term UI T745229
Date02/24/2009
LexicalTag NON
ThesaurusID

Congenital atransferrinemia MeSH Supplementary Concept Data 2024