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- Q7103623 subject Q6812688.
- Q7103623 subject Q6902466.
- Q7103623 subject Q7215445.
- Q7103623 abstract "Ornithine aminotransferase deficiency (also known as gyrate atrophy of the choroid and retina) is an inborn error of ornithine metabolism, caused by decreased activity of the enzyme ornithine aminotransferase. Biochemically, it can be detected by elevated levels of ornithine in the blood. Clinically, it presents initially with poor night vision, which slowly progresses to total blindness. It is believed to be inherited in an autosomal recessive manner. Approximately 200 known cases have been reported in the literature. The incidence is highest in Finland, estimated at 1:50,000.".
- Q7103623 omim "258870".
- Q7103623 thumbnail L-Ornithine_structure.svg?width=300.
- Q7103623 wikiPageWikiLink Q127724.
- Q7103623 wikiPageWikiLink Q1585743.
- Q7103623 wikiPageWikiLink Q161437.
- Q7103623 wikiPageWikiLink Q1640868.
- Q7103623 wikiPageWikiLink Q168403.
- Q7103623 wikiPageWikiLink Q18207833.
- Q7103623 wikiPageWikiLink Q1873857.
- Q7103623 wikiPageWikiLink Q2305910.
- Q7103623 wikiPageWikiLink Q3043161.
- Q7103623 wikiPageWikiLink Q33.
- Q7103623 wikiPageWikiLink Q40924.
- Q7103623 wikiPageWikiLink Q410198.
- Q7103623 wikiPageWikiLink Q425536.
- Q7103623 wikiPageWikiLink Q42918.
- Q7103623 wikiPageWikiLink Q463418.
- Q7103623 wikiPageWikiLink Q5223492.
- Q7103623 wikiPageWikiLink Q5353651.
- Q7103623 wikiPageWikiLink Q595994.
- Q7103623 wikiPageWikiLink Q6531938.
- Q7103623 wikiPageWikiLink Q6812688.
- Q7103623 wikiPageWikiLink Q681562.
- Q7103623 wikiPageWikiLink Q6902466.
- Q7103623 wikiPageWikiLink Q7103622.
- Q7103623 wikiPageWikiLink Q7103627.
- Q7103623 wikiPageWikiLink Q7187.
- Q7103623 wikiPageWikiLink Q7215445.
- Q7103623 wikiPageWikiLink Q737460.
- Q7103623 wikiPageWikiLink Q7758678.
- Q7103623 wikiPageWikiLink Q79749.
- Q7103623 wikiPageWikiLink Q8047.
- Q7103623 wikiPageWikiLink Q8066.
- Q7103623 wikiPageWikiLink Q80726.
- Q7103623 wikiPageWikiLink Q840737.
- Q7103623 name "Ornithine aminotransferase deficiency".
- Q7103623 omim "258870".
- Q7103623 type Disease.
- Q7103623 type Thing.
- Q7103623 type Q12136.
- Q7103623 comment "Ornithine aminotransferase deficiency (also known as gyrate atrophy of the choroid and retina) is an inborn error of ornithine metabolism, caused by decreased activity of the enzyme ornithine aminotransferase. Biochemically, it can be detected by elevated levels of ornithine in the blood. Clinically, it presents initially with poor night vision, which slowly progresses to total blindness. It is believed to be inherited in an autosomal recessive manner.".
- Q7103623 label "Ornithine aminotransferase deficiency".
- Q7103623 depiction L-Ornithine_structure.svg.
- Q7103623 name "Ornithine aminotransferase deficiency".