Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3242224> ?p ?o }
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- Q3242224 subject Q6902503.
- Q3242224 subject Q8408890.
- Q3242224 abstract "Congenital generalized lipodystrophy (also known as Berardinelli–Seip syndrome) is an extremely rare autosomal recessive skin condition, characterized by an extreme scarcity of fat in the subcutaneous tissues. Only 250 cases of the condition have been reported, and it is estimated that it occurs in 1 in 10 million people worldwide.".
- Q3242224 icd10 "E88.1".
- Q3242224 icd9 "272.6".
- Q3242224 meshId "D052497".
- Q3242224 omim "608594".
- Q3242224 wikiPageExternalLink ldconnect.org.
- Q3242224 wikiPageExternalLink br.fcgi?book=gene&part=bscl.
- Q3242224 wikiPageWikiLink Q1051872.
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- Q3242224 wikiPageWikiLink Q8408890.
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- Q3242224 icd "272.6".
- Q3242224 icd "E88.1".
- Q3242224 meshid "D052497".
- Q3242224 name "Congenital generalized lipodystrophy".
- Q3242224 omim "608594".
- Q3242224 type Disease.
- Q3242224 type Thing.
- Q3242224 type Q12136.
- Q3242224 comment "Congenital generalized lipodystrophy (also known as Berardinelli–Seip syndrome) is an extremely rare autosomal recessive skin condition, characterized by an extreme scarcity of fat in the subcutaneous tissues. Only 250 cases of the condition have been reported, and it is estimated that it occurs in 1 in 10 million people worldwide.".
- Q3242224 label "Congenital generalized lipodystrophy".
- Q3242224 name "Congenital generalized lipodystrophy".