Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q5037834> ?p ?o }
Showing triples 1 to 20 of
20
with 100 triples per page.
- Q5037834 subject Q6902466.
- Q5037834 subject Q7215445.
- Q5037834 abstract "Carbamoyl phosphate synthetase I deficiency (CPS I deficiency) is an autosomal recessive metabolic disorder that causes ammonia to accumulate in the blood due to a lack of the enzyme carbamoyl phosphate synthetase I. Ammonia, which is formed when proteins are broken down in the body, is toxic if the levels become too high. The nervous system is especially sensitive to the effects of excess ammonia.".
- Q5037834 thumbnail Autosomal_recessive_-_en.svg?width=300.
- Q5037834 wikiPageExternalLink NBK1217.
- Q5037834 wikiPageWikiLink Q1425030.
- Q5037834 wikiPageWikiLink Q186380.
- Q5037834 wikiPageWikiLink Q2351083.
- Q5037834 wikiPageWikiLink Q4087.
- Q5037834 wikiPageWikiLink Q425485.
- Q5037834 wikiPageWikiLink Q595994.
- Q5037834 wikiPageWikiLink Q627.
- Q5037834 wikiPageWikiLink Q6531938.
- Q5037834 wikiPageWikiLink Q6902466.
- Q5037834 wikiPageWikiLink Q7215445.
- Q5037834 wikiPageWikiLink Q9368.
- Q5037834 wikiPageWikiLink Q9404.
- Q5037834 comment "Carbamoyl phosphate synthetase I deficiency (CPS I deficiency) is an autosomal recessive metabolic disorder that causes ammonia to accumulate in the blood due to a lack of the enzyme carbamoyl phosphate synthetase I. Ammonia, which is formed when proteins are broken down in the body, is toxic if the levels become too high. The nervous system is especially sensitive to the effects of excess ammonia.".
- Q5037834 label "Carbamoyl phosphate synthetase I deficiency".
- Q5037834 depiction Autosomal_recessive_-_en.svg.
