Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q1678281> ?p ?o }
- Q1678281 wikiPageWikiLink Q847057.
- Q1678281 wikiPageWikiLink Q847583.
- Q1678281 wikiPageWikiLink Q85189.
- Q1678281 wikiPageWikiLink Q896643.
- Q1678281 wikiPageWikiLink Q91703.
- Q1678281 wikiPageWikiLink Q9368.
- Q1678281 wikiPageWikiLink Q9377.
- Q1678281 wikiPageWikiLink Q938107.
- Q1678281 wikiPageWikiLink Q9612.
- Q1678281 wikiPageWikiLink Q9631.
- Q1678281 wikiPageWikiLink Q978456.
- Q1678281 icd "759.89".
- Q1678281 icd "Q87.8".
- Q1678281 meshid "D020788".
- Q1678281 name "Bardet–Biedl syndrome".
- Q1678281 omim "209900".
- Q1678281 type Disease.
- Q1678281 type Thing.
- Q1678281 type Q12136.
- Q1678281 comment "Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet redirect here. See below for an explanation.Bardet–Biedl syndrome (BBS) is a ciliopathic human genetic disorder that produces many effects and affects many body systems. It is characterized principally by obesity, retinitis pigmentosa, polydactyly, hypogonadism, and renal failure in some cases. Historically, mental retardation has been considered a principal symptom but is now not regarded as such.".
- Q1678281 label "Bardet–Biedl syndrome".
- Q1678281 differentFrom Q3961678.
- Q1678281 name "Bardet–Biedl syndrome".