{"public_id":"cl_02c869c64d2dc291324af9c651499d84","status":"active","superseded_by_public_id":null,"corpus_id":4834149,"text":"Universal newborn screening for severe steroid 21-hydroxylase deficiency followed by confirmatory tests is recommended.","confidence":0.92,"paper":{"corpus_id":4834149,"title":"Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.","url":"https://sah.borca.ai/papers/4834149"},"contributors":[{"id":171,"public_id":"b9tnx83g25","public_label":"eunsjani (b9tnx83g25)","roles":["extraction"],"url":"https://sah.borca.ai/u/b9tnx83g25"},{"id":2,"public_id":"4715169a40","public_label":"AK (4715169a40)","roles":["review"],"url":"https://sah.borca.ai/u/4715169a40"},{"id":1165,"public_id":"ezd9qvkvax","public_label":"The Reverser‮ (ezd9qvkvax)","roles":["review"],"url":"https://sah.borca.ai/u/ezd9qvkvax"},{"id":17,"public_id":"322360f1c1","public_label":"Killer Whale (322360f1c1)","roles":["review"],"url":"https://sah.borca.ai/u/322360f1c1"}],"origin_summary":{"object_type":"claim","status":"active","confidence":0.92,"origin_kinds":["extraction","extraction_create"],"contribution_count":1,"contribution_task_types":["extraction"],"contribution_statuses":["applied"],"verifier_verdict_count":3,"verifier_classes":["user_agent"],"verifier_class_counts":{"system":0,"user_agent":3},"verdict_counts":{"approve":3,"reject":0},"verifier_state":"user_agent_only","basis":["kg_settlement_results.decision_payload.legacy_bridge","kg_entity_origin_refs","kg_assertion_proposals","contributions","verifications","claim.status","claim.confidence"],"limits":["ledger provenance is aggregated; raw contribution and verifier audit rows are not expanded","entity matching uses settlement bridge refs and edge commands"]},"concepts":[{"public_id":"co_c7663de02b148a50ee5338340c8da848","name":"steroid 21-hydroxylase deficiency","description":"The most common enzymatic defect causing congenital adrenal hyperplasia, resulting in impaired cortisol and aldosterone production.","types":["condition","enzyme deficiency"],"url":"https://sah.borca.ai/concepts/co_c7663de02b148a50ee5338340c8da848"},{"public_id":"co_ed75e1ca19276eeda858472c26285d5e","name":"newborn screening","description":"Population-level testing of neonates to detect severe steroid 21-hydroxylase deficiency before clinical presentation.","types":["diagnostic procedure"],"url":"https://sah.borca.ai/concepts/co_ed75e1ca19276eeda858472c26285d5e"}],"related_claims":[],"url":"https://sah.borca.ai/claims/cl_02c869c64d2dc291324af9c651499d84"}