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Bleeding Disorder Due To P2RY12 Defect MeSH Supplementary Concept Data 2022


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