MeSH Browser

MeSH Supplementary: Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant
Unique ID: C567347
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567347
Registry Numbers: 0
Heading Mapped to: *Protein S Deficiency
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant MeSH Supplementary Concept Data 2025