{"code":"C84960","name":"Ornithine Transcarbamylase Deficiency","terminology":"ncit","version":"26.10d","conceptStatus":"Retired_Concept","leaf":true,"active":false,"synonyms":[{"name":"Ornithine Transcarbamylase Deficiency","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Ornithine Transcarbamylase Deficiency","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"An X-linked urea cycle metabolic disorder characterized by deficiency of ornithine transcarbamylase, resulting in the accumulation of ammonia in the serum. Symptoms include vomiting, lethargy, and coma.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P310","type":"Concept_Status","value":"Retired_Concept"},{"code":"owl:deprecated","type":"deprecated","value":"true"},{"code":"P98","type":"DesignNote","value":"Mon Dec 10 17:40:13 EST 2012 - See 'Ornithine_Carbamoyltransferase_Deficiency_Disease'"},{"code":"P200","type":"OLD_PARENT","value":"Inborn_Urea_Cycle_Disorder"},{"code":"P106","type":"Semantic_Type","value":"Disease or Syndrome"}],"parents":[{"code":"C104171","name":"Retired Concept 2012"}]}