Matches in DBpedia 2016-04 for { ?s ?p "Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract. It is sporadic (i.e. it does not seem to be a hereditary disease), and it is currently considered acquired and idiopathic (i.e. cause remains unknown).About two-thirds of patients are of Japanese descent and the male to female ratio is 2:1. It was characterized in 1955."@en }
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- Cronkhite–Canada_syndrome abstract "Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract. It is sporadic (i.e. it does not seem to be a hereditary disease), and it is currently considered acquired and idiopathic (i.e. cause remains unknown).About two-thirds of patients are of Japanese descent and the male to female ratio is 2:1. It was characterized in 1955.".
- Q1422034 abstract "Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract. It is sporadic (i.e. it does not seem to be a hereditary disease), and it is currently considered acquired and idiopathic (i.e. cause remains unknown).About two-thirds of patients are of Japanese descent and the male to female ratio is 2:1. It was characterized in 1955.".
- Cronkhite–Canada_syndrome comment "Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract. It is sporadic (i.e. it does not seem to be a hereditary disease), and it is currently considered acquired and idiopathic (i.e. cause remains unknown).About two-thirds of patients are of Japanese descent and the male to female ratio is 2:1. It was characterized in 1955.".
- Q1422034 comment "Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract. It is sporadic (i.e. it does not seem to be a hereditary disease), and it is currently considered acquired and idiopathic (i.e. cause remains unknown).About two-thirds of patients are of Japanese descent and the male to female ratio is 2:1. It was characterized in 1955.".