Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3704732> ?p ?o }
Showing triples 1 to 37 of
37
with 100 triples per page.
- Q3704732 subject Q6853484.
- Q3704732 subject Q7216267.
- Q3704732 subject Q8732573.
- Q3704732 abstract "Antithrombin III deficiency (abbreviated ATIII deficiency) is a deficiency of antithrombin III. It is a rare hereditary disorder that generally comes to light when a patient suffers recurrent venous thrombosis and pulmonary embolism, and repetitive intrauterine fetal death (IUFD). Inheritance is usually autosomal dominant, though a few recessive cases have been noted.The disorder was first described by Egeberg in 1965.The patients are treated with anticoagulants or, more rarely, with antithrombin concentrate.In kidney failure, especially nephrotic syndrome, antithrombin is lost in the urine, leading to a higher activity of Factor II and Factor X and in increased tendency to thrombosis.".
- Q3704732 icd10 "D68.8".
- Q3704732 icd9 "289.81".
- Q3704732 meshId "D020152".
- Q3704732 omim "613118".
- Q3704732 wikiPageExternalLink PtAntithrombin.htm.
- Q3704732 wikiPageExternalLink www.nattinfo.org.
- Q3704732 wikiPageWikiLink Q14821011.
- Q3704732 wikiPageWikiLink Q14861061.
- Q3704732 wikiPageWikiLink Q14865111.
- Q3704732 wikiPageWikiLink Q186380.
- Q3704732 wikiPageWikiLink Q190016.
- Q3704732 wikiPageWikiLink Q200779.
- Q3704732 wikiPageWikiLink Q215118.
- Q3704732 wikiPageWikiLink Q220570.
- Q3704732 wikiPageWikiLink Q261327.
- Q3704732 wikiPageWikiLink Q476921.
- Q3704732 wikiPageWikiLink Q504790.
- Q3704732 wikiPageWikiLink Q6531938.
- Q3704732 wikiPageWikiLink Q6853484.
- Q3704732 wikiPageWikiLink Q7216267.
- Q3704732 wikiPageWikiLink Q8732573.
- Q3704732 wikiPageWikiLink Q929833.
- Q3704732 icd "289.81".
- Q3704732 icd "D68.8".
- Q3704732 meshid "D020152".
- Q3704732 name "Antithrombin III deficiency".
- Q3704732 omim "613118".
- Q3704732 type Disease.
- Q3704732 type Thing.
- Q3704732 type Q12136.
- Q3704732 comment "Antithrombin III deficiency (abbreviated ATIII deficiency) is a deficiency of antithrombin III. It is a rare hereditary disorder that generally comes to light when a patient suffers recurrent venous thrombosis and pulmonary embolism, and repetitive intrauterine fetal death (IUFD).".
- Q3704732 label "Antithrombin III deficiency".
- Q3704732 name "Antithrombin III deficiency".