| Source | us.cdc.phinvads#0.12.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.114222.4.11.7122 |
| canonical | http://phinvads.cdc.gov/fhir/ValueSet/2.16.840.1.114222.4.11.7122 |
| version | 1 |
| status | active |
| name | PHVS_NewbornCongenitalAnomalies_NCHS |
| title | Newborn Congenital Anomalies (NCHS) |
| date | 2013-01-28T00:06:00+11:00 |
| description | The value set contain the list of values use to specify malformations of the newborn diagnosed prenatally or after delivery. |
| Usages |
|
http://snomed.info/sct
version http://snomed.info/sct/731000124108/version/20200901
| Code | Display |
| 89369001 | Anencephaly |
| 67531005 | Meningomyelocele/Spina bifida |
| 12770006 | Cyanotic congenital heart disease |
| 17190001 | Congenital diaphragmatic hernia |
| 18735004 | Omphalocele |
| 72951007 | Gastroschisis |
| 67341007 | Limb reduction defect (excluding congenital amputation and dwarfing syndromes) |
| 80281008 | Cleft Lip with or without Cleft Palate |
| 87979003 | Cleft Palate alone |
| 70156005 | Down Syndrome |
| 409709004 | Suspected chromosomal disorder |
| 416010008 | Hypospadias |
| 260413007 | None of the specified items in this value set (including concept codes: 89369001, 67531005, 12770006, 17190001, 18735004, 72951007, 67341007, 67341007, 80281008, 87979003, 70156005, 409709004, 416010008) for Newborn Congenital Anomalies |
Produced 08 Sep 2023