MeSH Browser

MeSH Supplementary: Folate Malabsorption, Hereditary
Unique ID: C562799
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562799
Entry Term(s): Congenital Folate Malabsorption; Folic Acid Transport Defect; Hereditary Folate Malabsorption
Registry Numbers: 0
Heading Mapped to: *Folic Acid Deficiency; *Malabsorption Syndromes
Frequency: 21
Note: mutation in SLC46A1
Date of Entry: 2012/11/05
Revision Date: 2014/06/02

Concept UI: M0563099
Registry Numbers: 0
Terms: Folate Malabsorption, Hereditary Preferred Term
Term UI T801540
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hereditary Folate Malabsorption
Term UI T841595
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Congenital Folate Malabsorption
Term UI T841596
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Folic Acid Transport Defect
Term UI T841597
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Folate Malabsorption, Hereditary MeSH Supplementary Concept Data 2025