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- Q300801 subject Q6313232.
- Q300801 subject Q7004986.
- Q300801 subject Q8895551.
- Q300801 abstract "Aagenaes syndrome is a syndrome characterised by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts.The genetic cause is unknown, but it is autosomal recessively inherited and the gene is located to chromosome 15q1,2. A common feature of the condition is a generalised lymphatic anomaly, which may be indicative of the defect being lymphangiogenetic in origin1. The condition is particularly frequent in southern Norway, where more than half the cases are reported from, but is found in patients in other parts of Europe and the U.S.. It is named after Oystein Aagenaes, a Norwegian paediatrician.It is also called cholestasis-lymphedema syndrome (CLS).".
- Q300801 omim "214900".
- Q300801 wikiPageWikiLink Q1075923.
- Q300801 wikiPageWikiLink Q11238641.
- Q300801 wikiPageWikiLink Q13113715.
- Q300801 wikiPageWikiLink Q131742.
- Q300801 wikiPageWikiLink Q147778.
- Q300801 wikiPageWikiLink Q1568160.
- Q300801 wikiPageWikiLink Q16964430.
- Q300801 wikiPageWikiLink Q178694.
- Q300801 wikiPageWikiLink Q179630.
- Q300801 wikiPageWikiLink Q20.
- Q300801 wikiPageWikiLink Q2152526.
- Q300801 wikiPageWikiLink Q2604520.
- Q300801 wikiPageWikiLink Q30.
- Q300801 wikiPageWikiLink Q3508768.
- Q300801 wikiPageWikiLink Q46.
- Q300801 wikiPageWikiLink Q605709.
- Q300801 wikiPageWikiLink Q6313232.
- Q300801 wikiPageWikiLink Q6531938.
- Q300801 wikiPageWikiLink Q7004986.
- Q300801 wikiPageWikiLink Q727096.
- Q300801 wikiPageWikiLink Q8895551.
- Q300801 wikiPageWikiLink Q916398.
- Q300801 name "Aagenaes syndrome".
- Q300801 omim "214900".
- Q300801 type Disease.
- Q300801 type Thing.
- Q300801 type Q12136.
- Q300801 comment "Aagenaes syndrome is a syndrome characterised by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts.The genetic cause is unknown, but it is autosomal recessively inherited and the gene is located to chromosome 15q1,2.".
- Q300801 label "Aagenaes syndrome".
- Q300801 name "Aagenaes syndrome".