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- Q3508677 subject Q8432427.
- Q3508677 abstract "Mohr–Tranebjærg syndrome (MTS) is a rare X-liked recessive syndrome also known as Deafness-dystonia syndrome and caused by mutation in the TIMM8A gene. It was first described in 1960. The severity of the symptoms may vary, but they progress usually to severe deafness and dystonia and sometimes are accompanied by cortical deterioration of vision and mental deterioration.".
- Q3508677 omim "304700".
- Q3508677 wikiPageExternalLink condition=deafnessdystoniaopticneuronopathysyndrome.
- Q3508677 wikiPageExternalLink Summary.asp?File=10650.
- Q3508677 wikiPageExternalLink br.fcgi?book=gene&part=ddon.
- Q3508677 wikiPageWikiLink Q12133.
- Q3508677 wikiPageWikiLink Q162668.
- Q3508677 wikiPageWikiLink Q17913967.
- Q3508677 wikiPageWikiLink Q18038275.
- Q3508677 wikiPageWikiLink Q8432427.
- Q3508677 wikiPageWikiLink Q906492.
- Q3508677 wikiPageWikiLink Q935710.
- Q3508677 name "Mohr–Tranebjærg syndrome".
- Q3508677 omim "304700".
- Q3508677 type Disease.
- Q3508677 type Thing.
- Q3508677 type Q12136.
- Q3508677 comment "Mohr–Tranebjærg syndrome (MTS) is a rare X-liked recessive syndrome also known as Deafness-dystonia syndrome and caused by mutation in the TIMM8A gene. It was first described in 1960. The severity of the symptoms may vary, but they progress usually to severe deafness and dystonia and sometimes are accompanied by cortical deterioration of vision and mental deterioration.".
- Q3508677 label "Mohr–Tranebjærg syndrome".
- Q3508677 name "Mohr–Tranebjærg syndrome".