Birth And Fetal Death (BFDR) - STU2-ballot, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0-Preview1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-bfdr/ and changes regularly. See the Directory of published versions
Official URL: http://hl7.org/fhir/us/bfdr/ConceptMap/NewbornCongenitalAnomaliesCM | Version: 2.0.0-Preview1 | |||
Draft as of 2024-05-01 | Computable Name: NewbornCongenitalAnomalies | |||
Other Identifiers: OID:2.16.840.1.113883.4.642.40.13.18.12 | ||||
Usage:Clinical Focus: for IJE to FHIR alignment |
A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets
To help implementers map from IJE to FHIR Vocabulary
Mapping from (not specified) to Newborn Congenital Anomalies
DRAFT. Published on 2024-05-01 15:45:00+0000 by HL7 International / Public Health (HL7 International / Public Health: http://www.hl7.org/Special/com...).
A mapping between NCHS IJE and FHIR NewbornCongenitalAnomalies Value Sets
Group 1 Mapping from 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) |