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- Dysferlinopathy abstract "Dysferlinopathy is an autosomal recessive neuromuscular disorder caused by a deficiency of functional dysferlin protein due to mutations in the dysferlin gene. Dysferlinopathy is characterized by progressive muscle wasting and is most often clinically diagnosed as Limb-girdle muscular dystrophy type 2B (LGMD2B) or Miyoshi muscular dystrophy 1 (MMD1; a type of distal muscular dystrophy), depending on the initial pattern of muscle involvement at diagnosis. Dysferlinopathy is a rare disease, the exact incidence of which has not yet been determined.".
- Dysferlinopathy wikiPageExternalLink maltbrain.html.
- Dysferlinopathy wikiPageExternalLink www.jain-foundation.org.
- Dysferlinopathy wikiPageExternalLink NBK1303.
- Dysferlinopathy wikiPageExternalLink 253601.
- Dysferlinopathy wikiPageExternalLink 254130.
- Dysferlinopathy wikiPageID "27808317".
- Dysferlinopathy wikiPageLength "5064".
- Dysferlinopathy wikiPageOutDegree "9".
- Dysferlinopathy wikiPageRevisionID "678780395".
- Dysferlinopathy wikiPageWikiLink Category:Muscular_dystrophy.
- Dysferlinopathy wikiPageWikiLink Category:Rare_diseases.
- Dysferlinopathy wikiPageWikiLink Distal_muscular_dystrophy.
- Dysferlinopathy wikiPageWikiLink Dysferlin.
- Dysferlinopathy wikiPageWikiLink Jain_Foundation.
- Dysferlinopathy wikiPageWikiLink Limb-girdle_muscular_dystrophy.
- Dysferlinopathy wikiPageWikiLink Limb_girdles.
- Dysferlinopathy wikiPageWikiLink Miyoshi_muscular_dystrophy.
- Dysferlinopathy wikiPageWikiLink Skeletal_muscle.
- Dysferlinopathy wikiPageWikiLinkText "Dysferlinopathy".
- Dysferlinopathy wikiPageWikiLinkText "dysferlinopathy".
- Dysferlinopathy wikiPageUsesTemplate Template:Reflist.
- Dysferlinopathy subject Category:Muscular_dystrophy.
- Dysferlinopathy subject Category:Rare_diseases.
- Dysferlinopathy hypernym Disorder.
- Dysferlinopathy type Disease.
- Dysferlinopathy type Disorder.
- Dysferlinopathy comment "Dysferlinopathy is an autosomal recessive neuromuscular disorder caused by a deficiency of functional dysferlin protein due to mutations in the dysferlin gene. Dysferlinopathy is characterized by progressive muscle wasting and is most often clinically diagnosed as Limb-girdle muscular dystrophy type 2B (LGMD2B) or Miyoshi muscular dystrophy 1 (MMD1; a type of distal muscular dystrophy), depending on the initial pattern of muscle involvement at diagnosis.".
- Dysferlinopathy label "Dysferlinopathy".
- Dysferlinopathy sameAs Q3042104.
- Dysferlinopathy sameAs Dysferlinopathie.
- Dysferlinopathy sameAs m.0cc8mb6.
- Dysferlinopathy sameAs Q3042104.
- Dysferlinopathy wasDerivedFrom Dysferlinopathy?oldid=678780395.
- Dysferlinopathy isPrimaryTopicOf Dysferlinopathy.