{"code":"C99041","name":"Renal Agenesis","terminology":"ncit","version":"26.10d","conceptStatus":"DEFAULT","leaf":false,"active":true,"synonyms":[{"name":"Renal Agenesis","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"Cellosaurus"},{"name":"Renal Agenesis","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Renal Agenesis","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NICHD"},{"name":"Renal Agenesis","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"A congenital abnormality characterized by the absence of one or both kidneys.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"Cellosaurus"},{"code":"P322","type":"Contributing_Source","value":"NICHD"},{"code":"P106","type":"Semantic_Type","value":"Disease or Syndrome"},{"code":"P207","type":"UMLS_CUI","value":"C3805941"}],"parents":[{"code":"C98885","name":"Congenital Urinary System Abnormality"}],"roles":[{"code":"R108","type":"Disease_Has_Finding","relatedCode":"C53302","relatedName":"Congenital Lesion"},{"code":"R100","type":"Disease_Has_Associated_Anatomic_Site","relatedCode":"C12810","relatedName":"Genitourinary System"},{"code":"R101","type":"Disease_Has_Primary_Anatomic_Site","relatedCode":"C12810","relatedName":"Genitourinary System"},{"code":"R100","type":"Disease_Has_Associated_Anatomic_Site","relatedCode":"C12413","relatedName":"Urinary System"},{"code":"R101","type":"Disease_Has_Primary_Anatomic_Site","relatedCode":"C12413","relatedName":"Urinary System"}]}