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- Q7250337 subject Q6853484.
- Q7250337 subject Q6902466.
- Q7250337 subject Q7215445.
- Q7250337 subject Q8444063.
- Q7250337 abstract "Propionic acidemia, also known as propionic aciduria, propionyl-CoA carboxylase deficiency and ketotic glycinemia, is an autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia.The disorder presents in the early neonatal period with progressive encephalopathy. Death can occur quickly, due to secondary hyperammonemia, infection, cardiomyopathy, or basal ganglial stroke.Propionic acidemia is a rare disorder that is inherited from both parents. Being autosomal recessive, neither parent shows symptoms, but both carry a defective gene responsible for this disease. It takes two faulty genes to cause PA, so there is a 1 in 4 chance for these parents to have a child with PA.".
- Q7250337 icd10 "E71.1".
- Q7250337 icd9 "270.3".
- Q7250337 omim "606054".
- Q7250337 thumbnail Propionic_acid_structure.png?width=300.
- Q7250337 wikiPageExternalLink OC_Exp.php?Lng=EN&Expert=35.
- Q7250337 wikiPageExternalLink www.gwenforacure.com.
- Q7250337 wikiPageExternalLink www.oaanews.org.
- Q7250337 wikiPageExternalLink www.pafoundation.com.
- Q7250337 wikiPageExternalLink www.paresearch.org.
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- Q7250337 wikiPageWikiLink Q6853484.
- Q7250337 wikiPageWikiLink Q6902466.
- Q7250337 wikiPageWikiLink Q7187.
- Q7250337 wikiPageWikiLink Q7215445.
- Q7250337 wikiPageWikiLink Q7365.
- Q7250337 wikiPageWikiLink Q742500.
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- Q7250337 wikiPageWikiLink Q8066.
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- Q7250337 wikiPageWikiLink Q8444063.
- Q7250337 wikiPageWikiLink Q851.
- Q7250337 wikiPageWikiLink Q998.
- Q7250337 icd "270.3".
- Q7250337 icd "E71.1".
- Q7250337 name "Propionic acidemia".
- Q7250337 omim "606054".
- Q7250337 type Disease.
- Q7250337 type Thing.
- Q7250337 type Q12136.
- Q7250337 comment "Propionic acidemia, also known as propionic aciduria, propionyl-CoA carboxylase deficiency and ketotic glycinemia, is an autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia.The disorder presents in the early neonatal period with progressive encephalopathy. Death can occur quickly, due to secondary hyperammonemia, infection, cardiomyopathy, or basal ganglial stroke.Propionic acidemia is a rare disorder that is inherited from both parents.".
- Q7250337 label "Propionic acidemia".
- Q7250337 depiction Propionic_acid_structure.png.
- Q7250337 name "Propionic acidemia".