iminoglycinuria https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4985 https://rarediseases.info.nih.gov/diseases/8424/iminoglycinuria https://www.malacards.org/card/iminoglycinuria MONDO:0009448 iminoglycinuria Orphanet:42062 MESH:C536285 OMIM:242600 GARD:0008424 A metabolic disorder resulting from defective renal tube reabsorption of proline, hydroxyproline and glycine. The prevalence is estimated at around 1 in 15 000. The disorder is usually asymptomatic and is identified fortuitously by detection of increased levels of the imino acids and glycine in the urine. It is transmitted as an autosomal recessive trait. ICD9:270.8 icd11.foundation:664428532 DOID:0112265 UMLS:C0268654 SCTID:84121007 iminoglycinuria, digenic MEDGEN:124342 inborn disorder of amino acid transport