Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q744790> ?p ?o }
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- Q744790 subject Q6500135.
- Q744790 subject Q6853345.
- Q744790 subject Q6853484.
- Q744790 subject Q6907472.
- Q744790 subject Q7215483.
- Q744790 subject Q8690132.
- Q744790 abstract "Treacher Collins syndrome (TCS), also known as Treacher Collins–Franceschetti syndrome, or mandibulofacial dysostosis, is a rare autosomal dominant congenital disorder characterized by craniofacial deformities, such as absent cheekbones. Treacher Collins syndrome is found in about one in 50,000 births. The typical physical features include downward-slanting eyes, micrognathia (a small lower jaw), conductive hearing loss, underdeveloped zygoma, drooping part of the lateral lower eyelids, and malformed or absent ears.".
- Q744790 icd10 "Q75.4".
- Q744790 icd9 "756.0".
- Q744790 meshId "D008342".
- Q744790 omim "154500".
- Q744790 wikiPageExternalLink treacher-collins-syndrome.
- Q744790 wikiPageExternalLink www.earreconstructionspecialist.com.
- Q744790 wikiPageExternalLink www.friendlyfaces.org.
- Q744790 wikiPageExternalLink br.fcgi?book=gene&part=tcs.
- Q744790 wikiPageExternalLink www.tcsaroundtheworld.co.uk.
- Q744790 wikiPageExternalLink www.treachercollins.co.uk.
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- Q744790 icd "756".
- Q744790 icd "Q75.4".
- Q744790 meshid "D008342".
- Q744790 name "Treacher Collins syndrome".
- Q744790 omim "154500".
- Q744790 type Disease.
- Q744790 type Thing.
- Q744790 type Q12136.
- Q744790 comment "Treacher Collins syndrome (TCS), also known as Treacher Collins–Franceschetti syndrome, or mandibulofacial dysostosis, is a rare autosomal dominant congenital disorder characterized by craniofacial deformities, such as absent cheekbones. Treacher Collins syndrome is found in about one in 50,000 births.".
- Q744790 label "Treacher Collins syndrome".
- Q744790 name "Treacher Collins syndrome".