An organic aciduria caused by the deficient activity of the propionyl Coenzyme A carboxylase and is characterized by life threatening episodes of metabolic decompensation, neurological dysfunction and that may be complicated by cardiomyopathy.
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beta-ketothiolase deficiency
MONDO:0008760
3-hydroxyisobutyric aciduria
MONDO:0009371
isovaleric acidemia
MONDO:0009475
3-hydroxy-3-methylglutaric aciduria
MONDO:0009520
3-hydroxyisobutyryl-CoA hydrolase deficiency
MONDO:0009603
methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
MONDO:0009612