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


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 Number
0
Heading Mapped to
*Protein S Deficiency
Frequency
0
Date of Entry
2012/11/05
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant Preferred
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