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- Q822228 subject Q6902466.
- Q822228 subject Q7216267.
- Q822228 abstract "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets.".
- Q822228 icd10 "D69.1".
- Q822228 icd9 "287.1".
- Q822228 meshId "D001606".
- Q822228 omim "231200".
- Q822228 wikiPageExternalLink www.B-SS.org.
- Q822228 wikiPageExternalLink www.bernardsoulier.org.
- Q822228 wikiPageWikiLink Q101026.
- Q822228 wikiPageWikiLink Q14863678.
- Q822228 wikiPageWikiLink Q1529258.
- Q822228 wikiPageWikiLink Q1685256.
- Q822228 wikiPageWikiLink Q17110527.
- Q822228 wikiPageWikiLink Q18026313.
- Q822228 wikiPageWikiLink Q18026315.
- Q822228 wikiPageWikiLink Q18026323.
- Q822228 wikiPageWikiLink Q1914356.
- Q822228 wikiPageWikiLink Q202013.
- Q822228 wikiPageWikiLink Q487937.
- Q822228 wikiPageWikiLink Q5558486.
- Q822228 wikiPageWikiLink Q5598273.
- Q822228 wikiPageWikiLink Q574491.
- Q822228 wikiPageWikiLink Q585285.
- Q822228 wikiPageWikiLink Q611571.
- Q822228 wikiPageWikiLink Q6531938.
- Q822228 wikiPageWikiLink Q6902466.
- Q822228 wikiPageWikiLink Q709360.
- Q822228 wikiPageWikiLink Q7168670.
- Q822228 wikiPageWikiLink Q7216267.
- Q822228 wikiPageWikiLink Q821701.
- Q822228 wikiPageWikiLink Q890200.
- Q822228 wikiPageWikiLink Q904599.
- Q822228 wikiPageWikiLink Q928270.
- Q822228 icd "287.1".
- Q822228 icd "D69.1".
- Q822228 meshid "D001606".
- Q822228 name "Bernard-Soulier syndrome".
- Q822228 omim "231200".
- Q822228 type Disease.
- Q822228 type Thing.
- Q822228 type Q12136.
- Q822228 comment "Bernard–Soulier syndrome (BSS), also called hemorrhagiparous thrombocytic dystrophy, is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb), the receptor for von Willebrand factor, an important glycoprotein involved in hemostasis.The incidence of BSS is estimated to be less than 1 case per million persons, based on cases reported from Europe, North America, and Japan.BSS is a giant platelet disorder, meaning that it is characterized by abnormally large platelets.".
- Q822228 label "Bernard–Soulier syndrome".
- Q822228 name "Bernard-Soulier syndrome".