hyperdibasic aminoaciduria type 1 https://github.com/monarch-initiative/mondo/issues/4985 https://rarediseases.info.nih.gov/diseases/1854/dibasic-aminoaciduria-1 https://www.malacards.org/card/dibasic_amino_aciduria_i GARD:0001854 UMLS:C2673736 Orphanet:1032 Hyperdibasic aminoaciduria, type 1 is characterized by increased renal clearance of lysine, ornithine and arginine, in the presence of normal concentrations of cystine. Heterozygous individuals are asymptomatic but homozygotes display intellectual deficit. To date, 25 heterozygotes and one homozygote have been reported. dibasic aminoaciduria 1 dibasic amino aciduria type 1 OMIM:222690 icd11.foundation:1522058907 MEDGEN:435997 MESH:C567132 MONDO:0009108 inborn disorder of amino acid transport