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Hypodysfibrinogenemia, Congenital MeSH Supplementary Concept Data 2022


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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