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- Q1629483 subject Q6313232.
- Q1629483 subject Q6500135.
- Q1629483 subject Q6853484.
- Q1629483 subject Q6902466.
- Q1629483 subject Q6985910.
- Q1629483 subject Q7022837.
- Q1629483 abstract "Walker–Warburg syndrome (WWS), also called Warburg syndrome, Chemke syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD), is a rare form of autosomal recessive congenital muscular dystrophy. It is associated with brain (lissencephaly, hydrocephalus, cerebellar malformations) and eye abnormalities. This condition has a worldwide distribution. The overall incidence is unknown but a survey in North-eastern Italy has reported an incidence rate of 1.2 per 100,000 live births. It is the most severe form of congenital muscular dystrophy with most children dying before the age of three years.".
- Q1629483 omim "236670".
- Q1629483 thumbnail Autorecessive.svg?width=300.
- Q1629483 wikiPageWikiLink Q1137767.
- Q1629483 wikiPageWikiLink Q1473401.
- Q1629483 wikiPageWikiLink Q15319826.
- Q1629483 wikiPageWikiLink Q1544416.
- Q1629483 wikiPageWikiLink Q1753547.
- Q1629483 wikiPageWikiLink Q18035505.
- Q1629483 wikiPageWikiLink Q18039728.
- Q1629483 wikiPageWikiLink Q183560.
- Q1629483 wikiPageWikiLink Q186380.
- Q1629483 wikiPageWikiLink Q193003.
- Q1629483 wikiPageWikiLink Q409458.
- Q1629483 wikiPageWikiLink Q430024.
- Q1629483 wikiPageWikiLink Q4798559.
- Q1629483 wikiPageWikiLink Q5289104.
- Q1629483 wikiPageWikiLink Q6279182.
- Q1629483 wikiPageWikiLink Q6313232.
- Q1629483 wikiPageWikiLink Q6500135.
- Q1629483 wikiPageWikiLink Q6531938.
- Q1629483 wikiPageWikiLink Q6853484.
- Q1629483 wikiPageWikiLink Q6902466.
- Q1629483 wikiPageWikiLink Q6985910.
- Q1629483 wikiPageWikiLink Q7022837.
- Q1629483 wikiPageWikiLink Q727096.
- Q1629483 name "Walker–Warburg syndrome".
- Q1629483 omim "236670".
- Q1629483 type Disease.
- Q1629483 type Thing.
- Q1629483 type Q12136.
- Q1629483 comment "Walker–Warburg syndrome (WWS), also called Warburg syndrome, Chemke syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD), is a rare form of autosomal recessive congenital muscular dystrophy. It is associated with brain (lissencephaly, hydrocephalus, cerebellar malformations) and eye abnormalities. This condition has a worldwide distribution.".
- Q1629483 label "Walker–Warburg syndrome".
- Q1629483 depiction Autorecessive.svg.
- Q1629483 name "Walker–Warburg syndrome".