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- Q1507379 subject Q6902466.
- Q1507379 subject Q7215436.
- Q1507379 abstract "Nemaline myopathy (also called rod myopathy or nemaline rod myopathy) is a congenital, hereditary neuromuscular disorder that causes muscle weakness, generally nonprogressive, of varying severity. "Myopathy" means "muscle disease," and a biopsy of muscle from a person with nemaline myopathy shows abnormal thread-like rods, called nemaline bodies, in the muscle cells. People with nemaline myopathy (or NM) usually experience delayed motor development and weakness in the arm, leg, trunk, throat, and face muscles. The disorder is often clinically categorized into several groups, including mild (typical), intermediate, severe, and adult-onset; however, these distinctions are somewhat ambiguous, as the categories frequently overlap. Respiratory problems are a primary concern for people with all forms of NM, and though in some severe cases they may threaten life expectancy, aggressive and proactive care allows most individuals to survive and lead active lives. Nemaline myopathy is one of forty neuromuscular diseases covered by the Muscular Dystrophy Association.".
- Q1507379 icd10 "G71.2".
- Q1507379 icd9 "359.0".
- Q1507379 omim "161800".
- Q1507379 wikiPageExternalLink NBK1288.
- Q1507379 wikiPageExternalLink www.davidmcd.btinternet.co.uk.
- Q1507379 wikiPageExternalLink 0091902622.
- Q1507379 wikiPageExternalLink www.buildingstrength.org.
- Q1507379 wikiPageExternalLink nm.html.
- Q1507379 wikiPageExternalLink www.nemaline.org.
- Q1507379 wikiPageExternalLink rod.
- Q1507379 wikiPageExternalLink Nemaline_myopathy.
- Q1507379 wikiPageWikiLink Q1024207.
- Q1507379 wikiPageWikiLink Q1056395.
- Q1507379 wikiPageWikiLink Q106016.
- Q1507379 wikiPageWikiLink Q1087035.
- Q1507379 wikiPageWikiLink Q1234396.
- Q1507379 wikiPageWikiLink Q1641494.
- Q1507379 wikiPageWikiLink Q165328.
- Q1507379 wikiPageWikiLink Q17155582.
- Q1507379 wikiPageWikiLink Q174857.
- Q1507379 wikiPageWikiLink Q1753547.
- Q1507379 wikiPageWikiLink Q17709256.
- Q1507379 wikiPageWikiLink Q178694.
- Q1507379 wikiPageWikiLink Q179991.
- Q1507379 wikiPageWikiLink Q18032050.
- Q1507379 wikiPageWikiLink Q18032080.
- Q1507379 wikiPageWikiLink Q18032081.
- Q1507379 wikiPageWikiLink Q191931.
- Q1507379 wikiPageWikiLink Q241953.
- Q1507379 wikiPageWikiLink Q3117355.
- Q1507379 wikiPageWikiLink Q324921.
- Q1507379 wikiPageWikiLink Q5301925.
- Q1507379 wikiPageWikiLink Q6531938.
- Q1507379 wikiPageWikiLink Q6902466.
- Q1507379 wikiPageWikiLink Q6940370.
- Q1507379 wikiPageWikiLink Q7215436.
- Q1507379 wikiPageWikiLink Q727096.
- Q1507379 wikiPageWikiLink Q770609.
- Q1507379 wikiPageWikiLink Q813243.
- Q1507379 icd "359".
- Q1507379 icd "G71.2".
- Q1507379 omim "161800".
- Q1507379 type Disease.
- Q1507379 type Thing.
- Q1507379 type Q12136.
- Q1507379 comment "Nemaline myopathy (also called rod myopathy or nemaline rod myopathy) is a congenital, hereditary neuromuscular disorder that causes muscle weakness, generally nonprogressive, of varying severity. "Myopathy" means "muscle disease," and a biopsy of muscle from a person with nemaline myopathy shows abnormal thread-like rods, called nemaline bodies, in the muscle cells.".
- Q1507379 label "Nemaline myopathy".