| Source | ihe.pcc.aps#current:Antepartum Summary (v4.0.1) |
| resourceType | ValueSet |
| id | Antepartum.Family.History.and.Genetic.Screening.VS |
| canonical | https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS |
| version | 0.0.1-current |
| status | draft |
| publisher | IHE Patient Care Coordination Committee |
| name | Antepartum_Family_History_and_Genetic_Screening_VS |
| title | Antepartum Family History and Genetic Screening |
| date | 2023-08-01T19:32:25+00:00 |
| description | TBD |
| jurisdictions | uv |
| Usages | (none) |
http://snomed.info/sct
| Code | Display |
| 408856003 | Autism |
| 414022008 | Blood Disorders |
| 80544005 | Canavan Disease |
| 409709004 | Chromosomal Disorder Includes any inherited genetic or chromosomal disorders |
| 13213009 | Congenital Heart Defect |
| 190905008 | Cystic Fibrosis |
| 276720006 | Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects |
| 41040004 | Down Syndrome |
| 29159009 | Familial Dysautonomia |
| 90935002 | Hemophilia |
| 58756001 | Huntington's Chorea |
| 75934005 | Maternal Metabolic Disorder |
| 91138005 | Mental Retardation |
| 73297009 | Muscular Dystrophy |
| 253098009 | Neural Tube Defect |
| 102878001 | Recurrent pregnancy loss/stillbirth |
| 417357006 | Sickle Cell Disease |
| 16402000 | Sickle Cell Trait |
| 111385000 | Tay-Sachs |
| 40108008 | Thalassemia |
Produced 08 Sep 2023