MeSH Browser

MeSH Supplementary: Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant
Unique ID: C567163
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567163
Entry Term(s): PROC Deficiency, Autosomal Dominant; Protein C Deficiency, Autosomal Dominant
Registry Number: 0
Heading Mapped to: *Protein C Deficiency
Frequency: 0
Date of Entry: 2012/11/05

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant MeSH Supplementary Concept Data 2024