syndromic disease inherited amino acid metabolic disorder cystinuria (disease) CSNU Cystinuria is a renal tubular amino acid transport disorder characterized by recurrent formation of kidneys cystine stones. DOID:9266 GARD:0006237 HP:0003131 ICD10:E72.0 ICD10:E72.01 MESH:D003555 MONDO:0009067 MedDRA:10011778 NCIT:C84664 OMIM:220100 Orphanet:214 SCTID:85020001 UMLS:C0010691 cystinuria cystinuria, type A/B cystinuria, type B cystinuria, type I cystinuria, type I, formerly cystinuria, type II cystinuria, type II, formerly cystinuria, type III cystinuria, type III, formerly cystinuria, type a cystinuria, type non-I cystinuria, type non-I, formerly cystinuria-lysinuria cystinuria-lysinuria syndrome https://rarediseases.info.nih.gov/diseases/6237/cystinuria inherited renal tubular disease inborn disorder of amino acid absorption and transport rare renal tubular disease