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- Q3733697 subject Q7236984.
- Q3733697 abstract "Genetic heterogeneity is a phenomenon in which a single phenotype or genetic disorder may be caused by any one of a multiple number of alleles or non-allele (locus) mutations. This is in contrast to pleiotropy, where a single gene may cause multiple phenotypic expressions or disorders. Genetic heterogeneity describes genetic variation from the normal population. Clinically, genetic heterogeneity refers to diseases that result from multiple gene abnormalities. Multiple gene abnormalities are seen in disorders such as autism, cystic fibrosis, and retinitis pigmentosa.".
- Q3733697 wikiPageWikiLink Q104053.
- Q3733697 wikiPageWikiLink Q106016.
- Q3733697 wikiPageWikiLink Q106227.
- Q3733697 wikiPageWikiLink Q1134884.
- Q3733697 wikiPageWikiLink Q178194.
- Q3733697 wikiPageWikiLink Q38404.
- Q3733697 wikiPageWikiLink Q7236984.
- Q3733697 wikiPageWikiLink Q80726.
- Q3733697 wikiPageWikiLink Q847057.
- Q3733697 comment "Genetic heterogeneity is a phenomenon in which a single phenotype or genetic disorder may be caused by any one of a multiple number of alleles or non-allele (locus) mutations. This is in contrast to pleiotropy, where a single gene may cause multiple phenotypic expressions or disorders. Genetic heterogeneity describes genetic variation from the normal population. Clinically, genetic heterogeneity refers to diseases that result from multiple gene abnormalities.".
- Q3733697 label "Genetic heterogeneity".