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- Q3508642 subject Q6853484.
- Q3508642 subject Q6985910.
- Q3508642 abstract "Fukuyama congenital muscular dystrophy (FCMD) is a rare, autosomal recessive form of muscular dystrophy (weakness and breakdown of muscular tissue) mainly described in Japan but also identified in Turkish and Ashkenazi Jewish patients. Fifteen cases were first described in 1960 by Fukuyama.FCMD mainly affects the brain, eyes, and muscles. In particular, the disorder affects development of the skeletal muscles leading to weakness and deformed appearances, and brain development is blunted affecting cognitive functioning as well as social skills.In 1995, the disorder was linked to mutations in a gene coding for the protein fukutin (the FCMD gene).Fukuyama congenital muscular dystrophy is the second most prevalent form of muscular dystrophy in Japan. One out of every 90 people in Japan is a heterozygous carrier.".
- Q3508642 omim "253800".
- Q3508642 thumbnail Autosomal_recessive_-_en.svg?width=300.
- Q3508642 wikiPageExternalLink fukuyama-congenital-muscular-dystrophy.
- Q3508642 wikiPageExternalLink br.fcgi?book=gene&part=fcmd.
- Q3508642 wikiPageWikiLink Q1048687.
- Q3508642 wikiPageWikiLink Q1137767.
- Q3508642 wikiPageWikiLink Q1425030.
- Q3508642 wikiPageWikiLink Q1480291.
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- Q3508642 wikiPageWikiLink Q15319826.
- Q3508642 wikiPageWikiLink Q1544416.
- Q3508642 wikiPageWikiLink Q17.
- Q3508642 wikiPageWikiLink Q179991.
- Q3508642 wikiPageWikiLink Q186380.
- Q3508642 wikiPageWikiLink Q194520.
- Q3508642 wikiPageWikiLink Q285223.
- Q3508642 wikiPageWikiLink Q288280.
- Q3508642 wikiPageWikiLink Q308695.
- Q3508642 wikiPageWikiLink Q37748.
- Q3508642 wikiPageWikiLink Q6452282.
- Q3508642 wikiPageWikiLink Q6531938.
- Q3508642 wikiPageWikiLink Q6839941.
- Q3508642 wikiPageWikiLink Q6853484.
- Q3508642 wikiPageWikiLink Q6985910.
- Q3508642 wikiPageWikiLink Q7187.
- Q3508642 wikiPageWikiLink Q816759.
- Q3508642 wikiPageWikiLink Q840604.
- Q3508642 wikiPageWikiLink Q84133.
- Q3508642 name "Fukuyama congenital muscular dystrophy".
- Q3508642 omim "253800".
- Q3508642 type Disease.
- Q3508642 type Thing.
- Q3508642 type Q12136.
- Q3508642 comment "Fukuyama congenital muscular dystrophy (FCMD) is a rare, autosomal recessive form of muscular dystrophy (weakness and breakdown of muscular tissue) mainly described in Japan but also identified in Turkish and Ashkenazi Jewish patients. Fifteen cases were first described in 1960 by Fukuyama.FCMD mainly affects the brain, eyes, and muscles.".
- Q3508642 label "Fukuyama congenital muscular dystrophy".
- Q3508642 depiction Autosomal_recessive_-_en.svg.
- Q3508642 name "Fukuyama congenital muscular dystrophy".