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- Q638975 subject Q6853345.
- Q638975 subject Q7215436.
- Q638975 abstract "Central core disease (CCD), also known as central core myopathy, is an autosomal dominant congenital myopathy (inborn muscle disorder). It was first described by Shy and Magee in 1956. It is characterized by the appearance of the myofibril under the microscope.".
- Q638975 icd10 "G71.2".
- Q638975 icd9 "359.0".
- Q638975 meshId "D020512".
- Q638975 omim "117000".
- Q638975 thumbnail Cell_sample_of_muscle_tissue_with_central_core_disease_(stained_for_contrast).jpg?width=300.
- Q638975 wikiPageWikiLink Q1048687.
- Q638975 wikiPageWikiLink Q1074953.
- Q638975 wikiPageWikiLink Q112412.
- Q638975 wikiPageWikiLink Q1585081.
- Q638975 wikiPageWikiLink Q166543.
- Q638975 wikiPageWikiLink Q174857.
- Q638975 wikiPageWikiLink Q1753547.
- Q638975 wikiPageWikiLink Q179991.
- Q638975 wikiPageWikiLink Q186380.
- Q638975 wikiPageWikiLink Q2341604.
- Q638975 wikiPageWikiLink Q39572.
- Q638975 wikiPageWikiLink Q407784.
- Q638975 wikiPageWikiLink Q409458.
- Q638975 wikiPageWikiLink Q416781.
- Q638975 wikiPageWikiLink Q507369.
- Q638975 wikiPageWikiLink Q634638.
- Q638975 wikiPageWikiLink Q6531938.
- Q638975 wikiPageWikiLink Q6853345.
- Q638975 wikiPageWikiLink Q7215436.
- Q638975 wikiPageWikiLink Q767485.
- Q638975 wikiPageWikiLink Q8047.
- Q638975 icd "359".
- Q638975 icd "G71.2".
- Q638975 meshid "D020512".
- Q638975 name "Central Core Disease".
- Q638975 omim "117000".
- Q638975 type Disease.
- Q638975 type Thing.
- Q638975 type Q12136.
- Q638975 comment "Central core disease (CCD), also known as central core myopathy, is an autosomal dominant congenital myopathy (inborn muscle disorder). It was first described by Shy and Magee in 1956. It is characterized by the appearance of the myofibril under the microscope.".
- Q638975 label "Central core disease".
- Q638975 depiction Cell_sample_of_muscle_tissue_with_central_core_disease_(stained_for_contrast).jpg.
- Q638975 name "Central Core Disease".