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
Official URL: http://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM | Version: 2.0.0 | |||
Draft as of 2024-10-15 | Computable Name: NewbornCongenitalAnomalies | |||
Other Identifiers: OID:2.16.840.1.113883.4.642.40.13.18.11 | ||||
Usage:Clinical Focus: |
A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets
To help implementers map from IJE to FHIR Vocabulary
Generated Narrative: ConceptMap NewbornCongenitalAnomaliesCM
Mapping from ValueSet - Placeholder ValueSet for Interjurisdictional Exchange (IJE) in Vital Records to Newborn Congenital Anomalies
Group 1 Mapping from Code System - Placeholder Code System for IJE in Vital Records to SNOMED CT (all versions)
Source Code | Relationship | Target Code |
ANEN (Congenital Anomalies of the Newborn--Anencephaly) | is equivalent to | 89369001 (Anencephaly) |
MNSB (Congenital Anomalies of the Newborn--Meningomyelocele/Spina Bifida) | is equivalent to | 67531005 (Meningomyelocele/Spina bifida) |
CCHD (Congenital Anomalies of the Newborn--Cyanotic congenital heart disease) | is equivalent to | 12770006 (Cyanotic congenital heart disease) |
CDH (Congenital Anomalies of the Newborn--Congenital diaphragmatic hernia) | is equivalent to | 17190001 (Congenital diaphragmatic hernia) |
OMPH (Congenital Anomalies of the Newborn--Omphalocele) | is equivalent to | 18735004 (Omphalocele) |
GAST (Congenital Anomalies of the Newborn--Gastroschisis) | is equivalent to | 72951007 (Gastroschisis) |
LIMB (Congenital Anomalies of the Newborn--Limb Reduction Defect) | is equivalent to | 67341007 (Limb reduction defect (excluding congenital amputation and dwarfing syndromes)) |
CL (Congenital Anomalies of the Newborn--Cleft Lip with or without Cleft Palate) | is equivalent to | 80281008 (Cleft Lip with or without Cleft Palate) |
CP (Congenital Anomalies of the Newborn--Cleft Palate Alone) | is equivalent to | 87979003 (Cleft Palate alone) |
DOWT (Congenital Anomalies of the Newborn--Down Syndrome) | is equivalent to | 70156005 (Down Syndrome) |
CDIT (Congenital Anomalies of the Newborn--Suspected Chromosomal disorder) | is equivalent to | 409709004 (Suspected chromosomal disorder) |
HYPO (Congenital Anomalies of the Newborn--Hypospadias) | is equivalent to | 416010008 (Hypospadias) |