This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0-ballot: STU 2 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 1.1.0. For a full list of available versions, see the Directory of published versions
Generated Narrative: Condition
Resource Condition "condition-congenital-anomaly-of-newborn-babyg-quinn-2"
clinicalStatus: Active (Condition Clinical Status Codes#active)
category: Problem List Item (Condition Category Codes#problem-list-item), Congenital anomalies of the newborn [US Standard Certificate of Live Birth] (LOINC#73780-9)
code: Anomaly of chromosome pair 21 (disorder) (SNOMED CT#70156005)
subject: Patient/patient-child-babyg-quinn: Patient - Child (Baby G Quinn) " QUINN"
Code |
Karyotype determination pending (SNOMED CT#312948004 "Karyotype determination") |