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Folate Malabsorption, Hereditary MeSH Supplementary Concept Data 2024


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 Number
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
Folate Malabsorption, Hereditary Preferred
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