Epistaxis, Hereditary MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Epistaxis, Hereditary
Unique ID: C562751
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562751
Registry Numbers: 0
Heading Mapped to: *Epistaxis; *Genetic Diseases, Inborn
Frequency: 11
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Epistaxis, Hereditary Preferred

page delivered in 0.003s