Bleeding Disorder Due To P2RY12 Defect MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Bleeding Disorder Due To P2RY12 Defect
Unique ID: C565220
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565220
Registry Numbers: 0
Heading Mapped to: *Blood Coagulation Disorders, Inherited
Frequency: 0
Note: mutation in P2RY12
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Bleeding Disorder Due To P2RY12 Defect Preferred

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