FHIR IG Statistics: ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS
Resources that use this resource
No resources found
Resources that this resource uses
CodeSystem |
sct | SNOMED CT (all versions) |
sct | SNOMED codes used in this IG |
sct | veri |
Narrative
Note: links and images are rebased to the (stated) source
Source
{
"resourceType": "ValueSet",
"id": "Antepartum.Family.History.and.Genetic.Screening.VS",
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"url": "https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS",
"version": "0.0.1-current",
"name": "Antepartum_Family_History_and_Genetic_Screening_VS",
"title": "Antepartum Family History and Genetic Screening",
"status": "draft",
"experimental": false,
"date": "2023-10-24T22:43:25+00:00",
"publisher": "IHE Patient Care Coordination Committee",
"contact": [
{
"telecom": [
{
"system": "url",
"value": "https://www.ihe.net/ihe_domains/patient_care_coordination/"
}
]
},
{
"telecom": [
{
"system": "email",
"value": "pcc@ihe.net"
}
]
},
{
"name": "IHE Patient Care Coordination Committee",
"telecom": [
{
"system": "email",
"value": "pcc@ihe.net"
}
]
}
],
"description": "TBD",
"jurisdiction": [
{
"coding": [
{
"system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code": "001"
}
]
}
],
"compose": {
"include": [
{
"system": "http://snomed.info/sct",
"concept": [
{
"code": "408856003",
"display": "Autism"
},
{
"code": "414022008",
"display": "Blood Disorders"
},
{
"code": "80544005",
"display": "Canavan Disease"
},
{
"code": "409709004",
"display": "Chromosomal Disorder Includes any inherited genetic or chromosomal disorders"
},
{
"code": "13213009",
"display": "Congenital Heart Defect"
},
{
"code": "190905008",
"display": "Cystic Fibrosis"
},
{
"code": "276720006",
"display": "Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects"
},
{
"code": "41040004",
"display": "Down Syndrome"
},
{
"code": "29159009",
"display": "Familial Dysautonomia"
},
{
"code": "90935002",
"display": "Hemophilia"
},
{
"code": "58756001",
"display": "Huntington's Chorea"
},
{
"code": "75934005",
"display": "Maternal Metabolic Disorder"
},
{
"code": "91138005",
"display": "Mental Retardation"
},
{
"code": "73297009",
"display": "Muscular Dystrophy"
},
{
"code": "253098009",
"display": "Neural Tube Defect"
},
{
"code": "102878001",
"display": "Recurrent pregnancy loss/stillbirth"
},
{
"code": "417357006",
"display": "Sickle Cell Disease"
},
{
"code": "16402000",
"display": "Sickle Cell Trait"
},
{
"code": "111385000",
"display": "Tay-Sachs"
},
{
"code": "40108008",
"display": "Thalassemia"
}
]
}
]
}
}