MeSH Browser

MeSH Supplementary: Congenital thrombotic disease, due to Protein C deficiency
Unique ID: C535424
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535424
Entry Term(s): PROC deficiency; Thrombophilia, hereditary, due to pc deficiency
Registry Numbers: 0
Heading Mapped to: *Protein C Deficiency
Frequency: 8
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Congenital thrombotic disease, due to Protein C deficiency MeSH Supplementary Concept Data 2025