MeSH Browser

MeSH Supplementary: Intrinsic Factor Deficiency
Unique ID: C563242
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563242
Entry Term(s): Pernicious Anemia, Congenital, due to Defect of Intrinsic Factor
Heading Mapped to: Anemia, Pernicious / congenital; Intrinsic Factor / deficiency
Frequency: 9
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Intrinsic Factor Deficiency MeSH Supplementary Concept Data 2024