Hoffmann, "Mevalonate kinase deficiencies: from
mevalonic aciduria to hyperimmunoglobulinemia D syndrome," Orphanet Journal of Rare Diseases, vol.
(14.) Brucknerova I, Sebova C, Behulova D, Bzduch V, Mach M, Dubovicky M, et al:
Mevalonic aciduria as a cause of conjugated hyperbilirubinaemia in a case of term newborn.
Other compounds may also be quite specific, including 3-hydroxyglutarate for glutaric aciduria type I, mevalonic acid for
mevalonic aciduria, N-acetylaspartate for Canavan disease, 4-hydroxycyclohexylacetate for hawkinsinuria, and 2-ketoadipate and 2-hydroxyadipate for 2-amino/2-ketoadipate aciduria.