"DOID:0112265"^^ . "ORDO:42062"^^ . _:vb50946400 . . . . _:vb50946400 . "A renal tubular transport disease characterized by impaired renal tube reabsorption of proline, hydroxyproline and glycine and elevated urine levels of the imino acids and glycine that has_material_basis_in homozygous mutation in SLC36A2 on chromosome 5q33.1 combined with either heterozygous mutation in SLC6A20 gene on chromosome 3p21.31 or homozygous mutation in SLC6A19 on chromosome 5p15.33."^^ . "MESH:C536285"^^ . _:vb50946400 . "OMIM:242600"^^ . . _:vb50946400 . "GARD:8424"^^ . "iminoglycinuria"^^ . _:vb50946400 . "disease_ontology"^^ .