MeSH Browser

MeSH Supplementary: antithrombin III Rouen
Unique ID: C052332
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C052332
Entry Term(s): AT III Bligny; AT III Rouen; Rouen antithrombin III; antithrombin III Bligny
Registry Numbers: 0
Heading Mapped to: *Antithrombin III
Frequency: 2
Note: hereditary abnormal antithrombin; has heparin-binding defect; Arg at position 47 is replaced by His; same mutation reported in AT III Rouen and AT III Bligny
Source: Blood 1987;69(5):1275
Date of Entry: 1987/06/04
Revision Date: 2001/06/18

Concept UI: M0148582
Registry Numbers: 0
Terms: antithrombin III Rouen Preferred Term
Term UI T178587
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987); AT III Rouen
Term UI T178584
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987); Rouen antithrombin III
Term UI T178585
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987); antithrombin III Bligny
Term UI T178586
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987); AT III Bligny
Term UI T178583
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1987)

antithrombin III Rouen MeSH Supplementary Concept Data 2025