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- Q17028486 subject Q5881496.
- Q17028486 subject Q7063594.
- Q17028486 subject Q7215462.
- Q17028486 subject Q7297861.
- Q17028486 subject Q7469678.
- Q17028486 abstract "Hypomagnesemia with secondary hypocalcemia (HSH) is an autosomal recessive genetic disorder affecting intestinal magnesium absorption. Decreased intestinal magnesium reabsorption and the resulting decrease in serum magnesium levels is believed to cause lowered parathyroid hormone (PTH) output by the parathyroid gland. This results in decreased PTH and decreased serum calcium levels (hypocalcemia). This manifests in convulsions and spasms in early infancy which, if left untreated, can lead to mental retardation or death. HSH is caused by mutations in the TRPM6 gene.".
- Q17028486 omim "602014".
- Q17028486 wikiPageWikiLink Q1053120.
- Q17028486 wikiPageWikiLink Q1142188.
- Q17028486 wikiPageWikiLink Q14860476.
- Q17028486 wikiPageWikiLink Q14914571.
- Q17028486 wikiPageWikiLink Q1764062.
- Q17028486 wikiPageWikiLink Q183560.
- Q17028486 wikiPageWikiLink Q2051926.
- Q17028486 wikiPageWikiLink Q28745.
- Q17028486 wikiPageWikiLink Q3771629.
- Q17028486 wikiPageWikiLink Q511818.
- Q17028486 wikiPageWikiLink Q574360.
- Q17028486 wikiPageWikiLink Q5881496.
- Q17028486 wikiPageWikiLink Q61333.
- Q17028486 wikiPageWikiLink Q6279182.
- Q17028486 wikiPageWikiLink Q6431240.
- Q17028486 wikiPageWikiLink Q650401.
- Q17028486 wikiPageWikiLink Q6531938.
- Q17028486 wikiPageWikiLink Q658.
- Q17028486 wikiPageWikiLink Q660.
- Q17028486 wikiPageWikiLink Q706.
- Q17028486 wikiPageWikiLink Q7063594.
- Q17028486 wikiPageWikiLink Q7215462.
- Q17028486 wikiPageWikiLink Q7297861.
- Q17028486 wikiPageWikiLink Q7469678.
- Q17028486 wikiPageWikiLink Q790971.
- Q17028486 wikiPageWikiLink Q8066.
- Q17028486 wikiPageWikiLink Q840604.
- Q17028486 wikiPageWikiLink Q852376.
- Q17028486 wikiPageWikiLink Q936382.
- Q17028486 name "Hypomagnesemia with secondary hypocalcemia".
- Q17028486 omim "602014".
- Q17028486 type Disease.
- Q17028486 type Thing.
- Q17028486 type Q12136.
- Q17028486 comment "Hypomagnesemia with secondary hypocalcemia (HSH) is an autosomal recessive genetic disorder affecting intestinal magnesium absorption. Decreased intestinal magnesium reabsorption and the resulting decrease in serum magnesium levels is believed to cause lowered parathyroid hormone (PTH) output by the parathyroid gland. This results in decreased PTH and decreased serum calcium levels (hypocalcemia).".
- Q17028486 label "Hypomagnesemia with secondary hypocalcemia".
- Q17028486 name "Hypomagnesemia with secondary hypocalcemia".