Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3961685> ?p ?o }
Showing triples 1 to 45 of
45
with 100 triples per page.
- Q3961685 subject Q6500135.
- Q3961685 subject Q6853484.
- Q3961685 subject Q6902466.
- Q3961685 abstract "Rabson–Mendenhall syndrome is a rare autosomal recessive disorder characterized by severe insulin resistance. The disorder is caused by mutations in the insulin receptor gene. Symptoms include growth abnormalities of the head, face and nails, along with the development of acanthosis nigricans. Treatment involves controlling blood glucose levels by using insulin and incorporating a strategically planned, controlled diet. Also, direct actions against other symptoms may be taken (e.g. surgery for facial abnormalities) This syndrome usually affects children and has a prognosis of 1–2 years.".
- Q3961685 icd10 "E13".
- Q3961685 omim "262190".
- Q3961685 wikiPageWikiLink Q1128996.
- Q3961685 wikiPageWikiLink Q1130148.
- Q3961685 wikiPageWikiLink Q137835.
- Q3961685 wikiPageWikiLink Q14375936.
- Q3961685 wikiPageWikiLink Q14851942.
- Q3961685 wikiPageWikiLink Q14863356.
- Q3961685 wikiPageWikiLink Q14863714.
- Q3961685 wikiPageWikiLink Q16154261.
- Q3961685 wikiPageWikiLink Q1620594.
- Q3961685 wikiPageWikiLink Q1640998.
- Q3961685 wikiPageWikiLink Q1641068.
- Q3961685 wikiPageWikiLink Q19484.
- Q3961685 wikiPageWikiLink Q1968264.
- Q3961685 wikiPageWikiLink Q202758.
- Q3961685 wikiPageWikiLink Q21163221.
- Q3961685 wikiPageWikiLink Q224513.
- Q3961685 wikiPageWikiLink Q2467739.
- Q3961685 wikiPageWikiLink Q271993.
- Q3961685 wikiPageWikiLink Q3025883.
- Q3961685 wikiPageWikiLink Q365759.
- Q3961685 wikiPageWikiLink Q415833.
- Q3961685 wikiPageWikiLink Q417765.
- Q3961685 wikiPageWikiLink Q510786.
- Q3961685 wikiPageWikiLink Q641973.
- Q3961685 wikiPageWikiLink Q6500135.
- Q3961685 wikiPageWikiLink Q6531938.
- Q3961685 wikiPageWikiLink Q6853484.
- Q3961685 wikiPageWikiLink Q6902466.
- Q3961685 wikiPageWikiLink Q835051.
- Q3961685 wikiPageWikiLink Q877827.
- Q3961685 icd "E13".
- Q3961685 name "Rabson–Mendenhall syndrome".
- Q3961685 omim "262190".
- Q3961685 type Disease.
- Q3961685 type Thing.
- Q3961685 type Q12136.
- Q3961685 comment "Rabson–Mendenhall syndrome is a rare autosomal recessive disorder characterized by severe insulin resistance. The disorder is caused by mutations in the insulin receptor gene. Symptoms include growth abnormalities of the head, face and nails, along with the development of acanthosis nigricans. Treatment involves controlling blood glucose levels by using insulin and incorporating a strategically planned, controlled diet. Also, direct actions against other symptoms may be taken (e.g.".
- Q3961685 label "Rabson–Mendenhall syndrome".
- Q3961685 name "Rabson–Mendenhall syndrome".