HL7 PT FHIR Implementation Guide: Noticia de Nascimento
0.0.1 - STU1
HL7 PT FHIR Implementation Guide: Noticia de Nascimento
0.0.1 - STU1
HL7 PT FHIR Implementation Guide: Noticia de Nascimento, published by HL7 Portugal. This guide is not an authorized publication; it is the continuous build for version 0.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-pt/obs-neonat-ig/ and changes regularly. See the Directory of published versions
| Official URL: https://hl7.pt/fhir/NoticiaNascimento/ValueSet/newborn-congenital-anomalies-vs | Version: 0.0.1 | |||
| Active as of 2024-12-04 | Computable Name: NewbornCongenitalAnomaliesVS | |||
Tipos de doença congénita ValueSet
References
Generated Narrative: ValueSet newborn-congenital-anomalies-vs
http://snomed.info/sct| Code | Display |
| 89369001 | Anencephalus |
| 67531005 | Meningomyelocele/Spina bifida |
| 12770006 | Cyanotic congenital heart disease |
| 17190001 | Congenital diaphragmatic hernia |
| 18735004 | Congenital omphalocele |
| 72951007 | Gastroschisis |
| 67341007 | Longitudinal deficiency of limb - Limb reduction defect (excluding congenital amputation and dwarfing syndromes) |
| 80281008 | Cleft Lip with or without Cleft Palate |
| 87979003 | Cleft palate |
| 70156005 | Anomaly of chromosome pair 21 |
| 409709004 | Chromosomal disorder |
| 416010008 | Hypospadias |
| 282332003 | No abnormality detected - examination result |
Generated Narrative: ValueSet
Expansion based on SNOMED CT International edition 01-Aug 2024
This value set contains 13 concepts
| Code | System | Display |
| 89369001 | http://snomed.info/sct | Anencephalus |
| 67531005 | http://snomed.info/sct | Spina bifida |
| 12770006 | http://snomed.info/sct | Cyanotic congenital heart disease |
| 17190001 | http://snomed.info/sct | Congenital diaphragmatic hernia |
| 18735004 | http://snomed.info/sct | Congenital omphalocele |
| 72951007 | http://snomed.info/sct | Gastroschisis |
| 67341007 | http://snomed.info/sct | Longitudinal deficiency of limb |
| 80281008 | http://snomed.info/sct | Cleft lip |
| 87979003 | http://snomed.info/sct | Cleft palate |
| 70156005 | http://snomed.info/sct | Anomaly of chromosome pair 21 |
| 409709004 | http://snomed.info/sct | Chromosomal disorder (disorder) |
| 416010008 | http://snomed.info/sct | Hypospadias (disorder) |
| 282332003 | http://snomed.info/sct | No abnormality detected - examination result |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |