| Source | us.cdc.phinvads#0.12.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61 |
| canonical | http://phinvads.cdc.gov/fhir/ValueSet/1.3.6.1.4.1.19376.1.7.3.1.1.13.8.61 |
| version | 2 |
| status | active |
| name | PHVS_DownSyndrome_NCHS |
| title | Down Syndrome (NCHS) |
| date | 2014-01-22T00:09:00+11:00 |
| description | To reflect Down Syndrome as an anomaly of the newborn |
| Usages | (none) |
http://snomed.info/sct
version http://snomed.info/sct/731000124108/version/20200901
| Code | Display |
| 70156005 | Anomaly of chromosome pair 21 |
| 41040004 | Complete trisomy 21 syndrome |
| 205615000 | Trisomy 21- meiotic nondisjunction |
| 205616004 | Trisomy 21- mitotic nondisjunction mosaicism |
| 254264002 | Partial trisomy 21 in Down's syndrome |
| 371045000 | Translocation Down syndrome |
Produced 06 Apr 2023