2-hydroxyglutaric aciduria https://github.com/monarch-initiative/mondo/issues/6752 https://rarediseases.info.nih.gov/diseases/10761/2-hydroxyglutaric-aciduria https://www.malacards.org/card/2_hydroxyglutaric_aciduria GARD:0010761 MONDO:0016001 2-HGA MESH:C535306 UMLS:C2746066 DOID:0050573 2-hydroxyglutaric acidemia Orphanet:19 2-hydroxyglutaric aciduria 2-Hydroxyglutaric aciduria is a group of neurometabolic disorders with a wide clinical spectrum ranging from severe neonatal presentations to progressive forms, and asymptomatic cases, characterized biochemically by increased levels of 2-hydroxyglutaric acid in the plasma, cerebrospinal fluid and urine. MEDGEN:412535 NCIT:C128187 SCTID:698870008 ICD9:270.8 inborn errors of metabolism hereditary neurological disease