Ontology highlight
ABSTRACT:
SUBMITTER: Shakerdi LA
PROVIDER: S-EPMC10146379 | biostudies-literature | 2023 Apr
REPOSITORIES: biostudies-literature
Shakerdi Loai A LA Gillman Barbara B Corcoran Emma E McNulty Jenny J Treacy Eileen P EP
Metabolites 20230404 4
Organic acidurias are a heterogeneous group of rare inherited metabolic disorders (IMDs) caused by a deficiency of an enzyme or a transport protein involved in the intermediary metabolic pathways. These enzymatic defects lead to an accumulation of organic acids in different tissues and their subsequent excretion in urine. Organic acidurias include maple syrup urine disease, propionic aciduria, methylmalonic aciduria, isovaleric aciduria, and glutaric aciduria type 1. Clinical features vary betwe ...[more]