Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Blau_syndrome> ?p ?o }
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- Blau_syndrome abstract "Blau syndrome is characterized by familial granulomatous arthritis, uveitis, and skin granulomas, comprising an autosomal dominantly inherited syndrome that overlaps both sarcoidosis and granuloma annulare.Restated, Blau syndrome is a rare autosomal dominant disorder characterized by granulomatous polyarthritis, panuveitis, cranial neuropathies, and exanthema.Camptodactyly is another feature, and Crohn's disease occurs in 30%.It is associated with mutations in the NOD2 (a.k.a. CARD15) gene.".
- Blau_syndrome diseasesdb "32725".
- Blau_syndrome omim "186580".
- Blau_syndrome thumbnail Blau_syndrome2.jpg?width=300.
- Blau_syndrome wikiPageExternalLink malattieautoinfiammatorie.
- Blau_syndrome wikiPageID "20774636".
- Blau_syndrome wikiPageRevisionID "604578155".
- Blau_syndrome caption "Coarse facial features in a boy with Blau syndrome".
- Blau_syndrome diseasesdb "32725".
- Blau_syndrome hasPhotoCollection Blau_syndrome.
- Blau_syndrome omim "186580".
- Blau_syndrome subject Category:Autoinflammatory_syndromes.
- Blau_syndrome type Abstraction100002137.
- Blau_syndrome type Attribute100024264.
- Blau_syndrome type AutoinflammatorySyndromes.
- Blau_syndrome type Cognition100023271.
- Blau_syndrome type Complex105870365.
- Blau_syndrome type Concept105835747.
- Blau_syndrome type Condition113920835.
- Blau_syndrome type Content105809192.
- Blau_syndrome type Disease114070360.
- Blau_syndrome type Idea105833840.
- Blau_syndrome type IllHealth114052046.
- Blau_syndrome type Illness114061805.
- Blau_syndrome type PathologicalState114051917.
- Blau_syndrome type PhysicalCondition114034177.
- Blau_syndrome type PsychologicalFeature100023100.
- Blau_syndrome type State100024720.
- Blau_syndrome type Syndrome105870790.
- Blau_syndrome type Whole105869584.
- Blau_syndrome type Disease.
- Blau_syndrome type Situation.
- Blau_syndrome comment "Blau syndrome is characterized by familial granulomatous arthritis, uveitis, and skin granulomas, comprising an autosomal dominantly inherited syndrome that overlaps both sarcoidosis and granuloma annulare.Restated, Blau syndrome is a rare autosomal dominant disorder characterized by granulomatous polyarthritis, panuveitis, cranial neuropathies, and exanthema.Camptodactyly is another feature, and Crohn's disease occurs in 30%.It is associated with mutations in the NOD2 (a.k.a. CARD15) gene.".
- Blau_syndrome label "Blau syndrome".
- Blau_syndrome label "Blau-Syndrom".
- Blau_syndrome label "Zespół Blaua".
- Blau_syndrome label "متلازمة بلاو".
- Blau_syndrome sameAs Blau-Syndrom.
- Blau_syndrome sameAs Zespół_Blaua.
- Blau_syndrome sameAs m.056z2m_.
- Blau_syndrome sameAs Q441077.
- Blau_syndrome sameAs Q441077.
- Blau_syndrome sameAs 158.
- Blau_syndrome sameAs Blau_syndrome.
- Blau_syndrome wasDerivedFrom Blau_syndrome?oldid=604578155.
- Blau_syndrome depiction Blau_syndrome2.jpg.
- Blau_syndrome isPrimaryTopicOf Blau_syndrome.