This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0: STU2) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
Generated Narrative: Condition condition-congenital-anomaly-of-newborn-babyg-quinn-2
clinicalStatus: Active
category: Problem List Item, Congenital anomalies of the newborn [US Standard Certificate of Live Birth]
code: Anomaly of chromosome pair 21 (disorder)
subject: Patient - Child (Baby G Quinn)
Code |
Karyotype determination pending |