Epistaxis, Hereditary MeSH Supplementary Concept Data 2024

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Concepts

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

Epistaxis, Hereditary Preferred

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