MeSH Browser

MeSH Supplementary: Lp(A) Deficiency, Congenital
Unique ID: C563618
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563618
Entry Term(s): Lipoprotein(A) Deficiency, Congenital
Registry Number: 0
Heading Mapped to: *Lipid Metabolism, Inborn Errors; Lipoprotein(a) / *deficiency
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Lp(A) Deficiency, Congenital MeSH Supplementary Concept Data 2024