Hypodysfibrinogenemia, Congenital MeSH Supplementary Concept Data 2023

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Concepts

MeSH Supplementary: Hypodysfibrinogenemia, Congenital
Unique ID: C565970
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565970
Registry Number: 0
Heading Mapped to: *Afibrinogenemia
Frequency: 12
Date of Entry: 2012/11/05

Hypodysfibrinogenemia, Congenital Preferred

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