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- Primrose_syndrome abstract "Primrose syndrome is a rare, slowly progressive genetic disorder that can vary symptomatically between individual cases, but is generally characterised by ossification of the external ears, learning difficulties, and facial abnormalities. It was first described in 1982 in Scotland's Royal National Larbert Institution by Dr D.A.A. Primrose.Primrose syndrome appears to occur spontaneously, regardless of family history. The cause is currently unknown and there are no known treatments.".
- Primrose_syndrome omim "259050".
- Primrose_syndrome wikiPageExternalLink 259050.
- Primrose_syndrome wikiPageExternalLink pdf-preview.axd?code=ql5xbcv0t89b0vt9&size=largest.
- Primrose_syndrome wikiPageExternalLink syndrome_cgibd2d.html.
- Primrose_syndrome wikiPageID "1256552".
- Primrose_syndrome wikiPageLength "7711".
- Primrose_syndrome wikiPageOutDegree "37".
- Primrose_syndrome wikiPageRevisionID "609286803".
- Primrose_syndrome wikiPageWikiLink Agenesis_of_the_corpus_callosum.
- Primrose_syndrome wikiPageWikiLink Ataxia.
- Primrose_syndrome wikiPageWikiLink Auricle_(anatomy).
- Primrose_syndrome wikiPageWikiLink Basal_ganglia.
- Primrose_syndrome wikiPageWikiLink Calcinosis.
- Primrose_syndrome wikiPageWikiLink Calcitonin.
- Primrose_syndrome wikiPageWikiLink Category:Genetic_disorders.
- Primrose_syndrome wikiPageWikiLink Category:Rare_diseases.
- Primrose_syndrome wikiPageWikiLink Category:Systemic_connective_tissue_disorders.
- Primrose_syndrome wikiPageWikiLink Chromosome_11_(human).
- Primrose_syndrome wikiPageWikiLink Congenital_heart_defect.
- Primrose_syndrome wikiPageWikiLink Contracture.
- Primrose_syndrome wikiPageWikiLink Cryptorchidism.
- Primrose_syndrome wikiPageWikiLink DNA_microarray.
- Primrose_syndrome wikiPageWikiLink Diabetes_mellitus.
- Primrose_syndrome wikiPageWikiLink Ebsteins_anomaly.
- Primrose_syndrome wikiPageWikiLink External_ear.
- Primrose_syndrome wikiPageWikiLink Fahrs_syndrome.
- Primrose_syndrome wikiPageWikiLink Genetic_disorder.
- Primrose_syndrome wikiPageWikiLink Hip_dysplasia.
- Primrose_syndrome wikiPageWikiLink Hip_dysplasia_(human).
- Primrose_syndrome wikiPageWikiLink Hypothyroidism.
- Primrose_syndrome wikiPageWikiLink Intellectual_disability.
- Primrose_syndrome wikiPageWikiLink Magnetic_resonance_imaging_of_the_brain.
- Primrose_syndrome wikiPageWikiLink Mental_retardation.
- Primrose_syndrome wikiPageWikiLink Muscle_atrophy.
- Primrose_syndrome wikiPageWikiLink Muscular_atrophy.
- Primrose_syndrome wikiPageWikiLink Neoplasm.
- Primrose_syndrome wikiPageWikiLink Online_Mendelian_Inheritance_in_Man.
- Primrose_syndrome wikiPageWikiLink Ossification.
- Primrose_syndrome wikiPageWikiLink Outer_ear.
- Primrose_syndrome wikiPageWikiLink Paraparesis.
- Primrose_syndrome wikiPageWikiLink Paraplegia.
- Primrose_syndrome wikiPageWikiLink Parkinsonism.
- Primrose_syndrome wikiPageWikiLink Pinna_(anatomy).
- Primrose_syndrome wikiPageWikiLink Royal_National_Larbert_Institution.
- Primrose_syndrome wikiPageWikiLink Scotland.
- Primrose_syndrome wikiPageWikiLink Thyroid.
- Primrose_syndrome wikiPageWikiLink Torus_palatinus.
- Primrose_syndrome wikiPageWikiLink United_States_National_Library_of_Medicine.
- Primrose_syndrome wikiPageWikiLinkText "Primrose syndrome".
- Primrose_syndrome hasPhotoCollection Primrose_syndrome.
- Primrose_syndrome name "Primrose syndrome".
- Primrose_syndrome omim "259050".
- Primrose_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Primrose_syndrome wikiPageUsesTemplate Template:Reflist.
- Primrose_syndrome subject Category:Genetic_disorders.
- Primrose_syndrome subject Category:Rare_diseases.
- Primrose_syndrome subject Category:Systemic_connective_tissue_disorders.
- Primrose_syndrome type Disease.
- Primrose_syndrome type Disorder.
- Primrose_syndrome type Thing.
- Primrose_syndrome type Q12136.
- Primrose_syndrome comment "Primrose syndrome is a rare, slowly progressive genetic disorder that can vary symptomatically between individual cases, but is generally characterised by ossification of the external ears, learning difficulties, and facial abnormalities. It was first described in 1982 in Scotland's Royal National Larbert Institution by Dr D.A.A. Primrose.Primrose syndrome appears to occur spontaneously, regardless of family history. The cause is currently unknown and there are no known treatments.".
- Primrose_syndrome label "Primrose syndrome".
- Primrose_syndrome sameAs m.04mpjl.
- Primrose_syndrome sameAs Q7243682.
- Primrose_syndrome sameAs Q7243682.
- Primrose_syndrome wasDerivedFrom Primrose_syndrome?oldid=609286803.
- Primrose_syndrome isPrimaryTopicOf Primrose_syndrome.
- Primrose_syndrome name "Primrose syndrome".