has material basis in germline mutation in GCDH glutaric aciduria inborn organic aciduria glutaryl-CoA dehydrogenase deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4985 https://github.com/monarch-initiative/mondo/issues/6752 https://www.malacards.org/card/glutaric_acidemia_i glutaric acidemia type 1 NANDO:1200800 MESH:C536833 GCDHD SCTID:76175005 GA1 OMIM:231670 glutaryl-CoA dehydrogenase deficiency MONDO:0009281 Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder. NANDO:2200501 GARD:0006522 glutaricaciduria, type I glutaric acidemia type I DOID:0111254 glutaric aciduria, type 1 UMLS:C0268595 NCIT:C99101 MEDGEN:124337 glutaric aciduria type 1 glutaryl-coenzyme A dehydrogenase deficiency glutaric acidemia 1 Orphanet:25 hereditary neurological disease