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- Q112412 subject Q6902503.
- Q112412 subject Q7215436.
- Q112412 abstract "Congenital myopathy is a very broad term for any muscle disorder present at birth. This defect primarily affects skeletal muscle fibres and causes muscular weakness and/or hypotonia. Congenital myopathies account for one of the top neuromuscular disorders in the world today, comprising approximately 6 in 100,000 live births every year. As a whole, congenital myopathies can be broadly classified as follows:A distinctive abnormality in skeletal muscle fibres on the cellular level; observable via light microscopeSymptoms of muscle weakness and hypotonia Is a congenital disorder, meaning it occurs during development and symptoms present themselves at birth or in early life.Is a genetic disorder.↑".
- Q112412 icd10 "G71.2".
- Q112412 icd9 "359.0".
- Q112412 meshId "D020914".
- Q112412 wikiPageExternalLink br.fcgi?book=gene&part=cftd.
- Q112412 wikiPageExternalLink www.znm-zusammenstark.org.
- Q112412 wikiPageWikiLink Q1308970.
- Q112412 wikiPageWikiLink Q1507379.
- Q112412 wikiPageWikiLink Q1585081.
- Q112412 wikiPageWikiLink Q1753547.
- Q112412 wikiPageWikiLink Q17825605.
- Q112412 wikiPageWikiLink Q17833164.
- Q112412 wikiPageWikiLink Q17914045.
- Q112412 wikiPageWikiLink Q18031340.
- Q112412 wikiPageWikiLink Q18042972.
- Q112412 wikiPageWikiLink Q28775.
- Q112412 wikiPageWikiLink Q40260.
- Q112412 wikiPageWikiLink Q409458.
- Q112412 wikiPageWikiLink Q410251.
- Q112412 wikiPageWikiLink Q412837.
- Q112412 wikiPageWikiLink Q507369.
- Q112412 wikiPageWikiLink Q5160430.
- Q112412 wikiPageWikiLink Q597678.
- Q112412 wikiPageWikiLink Q638975.
- Q112412 wikiPageWikiLink Q6531938.
- Q112412 wikiPageWikiLink Q6902503.
- Q112412 wikiPageWikiLink Q7215436.
- Q112412 wikiPageWikiLink Q782958.
- Q112412 wikiPageWikiLink Q79927.
- Q112412 wikiPageWikiLink Q906704.
- Q112412 icd "359".
- Q112412 icd "G71.2".
- Q112412 meshid "D020914".
- Q112412 name "Congenital Myopathy".
- Q112412 type Disease.
- Q112412 type Thing.
- Q112412 type Q12136.
- Q112412 comment "Congenital myopathy is a very broad term for any muscle disorder present at birth. This defect primarily affects skeletal muscle fibres and causes muscular weakness and/or hypotonia. Congenital myopathies account for one of the top neuromuscular disorders in the world today, comprising approximately 6 in 100,000 live births every year.".
- Q112412 label "Congenital myopathy".
- Q112412 name "Congenital Myopathy".