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- Smith_Martin_Dodd_syndrome abstract "Smith Martin Dodd syndrome is a very rare genetic disorder first described by Smith et al. in 1994. It is characterized by small eyes, a diaphragmatic hernia, and Tetralogy of Fallot, a congenital heart defect. The only known case is of a 9-year-old boy with several congenital anomalies including a diaphragmatic hernia, microphthalmia, and Tetralogy of Fallot. It was found that the boy had a reciprocal translocation t(1;15)(q41;q21.2). A congenital diaphragmatic hernia is consistent with chromosome 1q41-q42 deletion syndrome, and the report by Smith et al. suggested that genes involved in the translocation may be important for the development of morphological characteristics, especially those of the eye or heart.".
- Smith_Martin_Dodd_syndrome wikiPageID "33594136".
- Smith_Martin_Dodd_syndrome wikiPageLength "2091".
- Smith_Martin_Dodd_syndrome wikiPageOutDegree "8".
- Smith_Martin_Dodd_syndrome wikiPageRevisionID "610352672".
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Category:Cardiogenetic_disorders.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Category:Genetic_disorders.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Category:Rare_diseases.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Chromosomal_translocation.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Congenital_heart_defect.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Diaphragmatic_hernia.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Microphthalmia.
- Smith_Martin_Dodd_syndrome wikiPageWikiLink Tetralogy_of_Fallot.
- Smith_Martin_Dodd_syndrome hasPhotoCollection Smith_Martin_Dodd_syndrome.
- Smith_Martin_Dodd_syndrome wikiPageUsesTemplate Template:Disease-stub.
- Smith_Martin_Dodd_syndrome wikiPageUsesTemplate Template:Reflist.
- Smith_Martin_Dodd_syndrome subject Category:Cardiogenetic_disorders.
- Smith_Martin_Dodd_syndrome subject Category:Genetic_disorders.
- Smith_Martin_Dodd_syndrome subject Category:Rare_diseases.
- Smith_Martin_Dodd_syndrome type Disease.
- Smith_Martin_Dodd_syndrome type Disorder.
- Smith_Martin_Dodd_syndrome type Thing.
- Smith_Martin_Dodd_syndrome type Q12136.
- Smith_Martin_Dodd_syndrome comment "Smith Martin Dodd syndrome is a very rare genetic disorder first described by Smith et al. in 1994. It is characterized by small eyes, a diaphragmatic hernia, and Tetralogy of Fallot, a congenital heart defect. The only known case is of a 9-year-old boy with several congenital anomalies including a diaphragmatic hernia, microphthalmia, and Tetralogy of Fallot. It was found that the boy had a reciprocal translocation t(1;15)(q41;q21.2).".
- Smith_Martin_Dodd_syndrome label "Smith Martin Dodd syndrome".
- Smith_Martin_Dodd_syndrome sameAs m.0hgll1k.
- Smith_Martin_Dodd_syndrome sameAs Q17124192.
- Smith_Martin_Dodd_syndrome sameAs Q17124192.
- Smith_Martin_Dodd_syndrome wasDerivedFrom Smith_Martin_Dodd_syndrome?oldid=610352672.
- Smith_Martin_Dodd_syndrome isPrimaryTopicOf Smith_Martin_Dodd_syndrome.