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- Q419897 subject Q6902466.
- Q419897 subject Q6949571.
- Q419897 subject Q8750387.
- Q419897 abstract "Aminolevulinic acid dehydratase deficiency porphyria (also known as "Doss porphyria," and "Plumboporphyria") is a cutaneous condition, disease can present during early childhood (as well as in adulthood) with acute neurologic symptoms that resemble those encountered in acute intermittent porphyria. The condition is extremely rare, with fewer than 10 cases ever reported.ALA dehydratase deficiency is a rare cause of hepatic porphyria. It is an autosomal recessive disorder that results from inappropriately low levels of the enzyme ALA dehydratase (ALAD, also called porphobilinogen synthase), which is required for normal heme synthesis.".
- Q419897 thumbnail Autorecessive.svg?width=300.
- Q419897 wikiPageWikiLink Q1425030.
- Q419897 wikiPageWikiLink Q186380.
- Q419897 wikiPageWikiLink Q189621.
- Q419897 wikiPageWikiLink Q246809.
- Q419897 wikiPageWikiLink Q289302.
- Q419897 wikiPageWikiLink Q3908490.
- Q419897 wikiPageWikiLink Q6531938.
- Q419897 wikiPageWikiLink Q6902466.
- Q419897 wikiPageWikiLink Q6949571.
- Q419897 wikiPageWikiLink Q8750387.
- Q419897 comment "Aminolevulinic acid dehydratase deficiency porphyria (also known as "Doss porphyria," and "Plumboporphyria") is a cutaneous condition, disease can present during early childhood (as well as in adulthood) with acute neurologic symptoms that resemble those encountered in acute intermittent porphyria. The condition is extremely rare, with fewer than 10 cases ever reported.ALA dehydratase deficiency is a rare cause of hepatic porphyria.".
- Q419897 label "Aminolevulinic acid dehydratase deficiency porphyria".
- Q419897 depiction Autorecessive.svg.