MeSH Browser

MeSH Supplementary: Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive
Unique ID: C567348
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567348
Registry Number: 0
Heading Mapped to: *Protein S Deficiency
Frequency: 1
Date of Entry: 2012/11/05

Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive MeSH Supplementary Concept Data 2024