Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q365589> ?p ?o }
Showing triples 1 to 37 of
37
with 100 triples per page.
- Q365589 subject Q16813146.
- Q365589 subject Q6500135.
- Q365589 subject Q8733695.
- Q365589 abstract "XX male syndrome (also called de la Chapelle syndrome, for Albert de la Chapelle, who characterized it in 1972) is a rare sex chromosomal disorder. Usually, it is caused by unequal crossing over between X and Y chromosomes during meiosis in the father, which results in the X chromosome containing the normally-male SRY gene. When this X combines with a normal X from the mother during fertilization, the result is an XX male.This syndrome occurs in approximately four or five in 100,000 individuals, making it less common than Klinefelter syndrome.".
- Q365589 icd10 "(Q98.3)".
- Q365589 omim "278850".
- Q365589 wikiPageExternalLink NBK1416.
- Q365589 wikiPageExternalLink NBK1547.
- Q365589 wikiPageWikiLink Q1132108.
- Q365589 wikiPageWikiLink Q118406.
- Q365589 wikiPageWikiLink Q14819281.
- Q365589 wikiPageWikiLink Q162925.
- Q365589 wikiPageWikiLink Q16813146.
- Q365589 wikiPageWikiLink Q179399.
- Q365589 wikiPageWikiLink Q189967.
- Q365589 wikiPageWikiLink Q202771.
- Q365589 wikiPageWikiLink Q207133.
- Q365589 wikiPageWikiLink Q244145.
- Q365589 wikiPageWikiLink Q339221.
- Q365589 wikiPageWikiLink Q491057.
- Q365589 wikiPageWikiLink Q512313.
- Q365589 wikiPageWikiLink Q5618748.
- Q365589 wikiPageWikiLink Q61333.
- Q365589 wikiPageWikiLink Q640652.
- Q365589 wikiPageWikiLink Q6500135.
- Q365589 wikiPageWikiLink Q8733695.
- Q365589 wikiPageWikiLink Q912422.
- Q365589 wikiPageWikiLink Q9384.
- Q365589 wikiPageWikiLink Q957751.
- Q365589 name "XX male syndrome".
- Q365589 omim "278850".
- Q365589 type Disease.
- Q365589 type Thing.
- Q365589 type Q12136.
- Q365589 comment "XX male syndrome (also called de la Chapelle syndrome, for Albert de la Chapelle, who characterized it in 1972) is a rare sex chromosomal disorder. Usually, it is caused by unequal crossing over between X and Y chromosomes during meiosis in the father, which results in the X chromosome containing the normally-male SRY gene.".
- Q365589 label "XX male syndrome".
- Q365589 name "XX male syndrome".