FHIR IG Statistics: ValueSet/vs-icd10-predisposition-eu-pcsp
Resources that use this resource
Resources that this resource uses
Narrative
Note: links and images are rebased to the (stated) source
This value set includes codes based on the following rules:
- Include these codes as defined in
http://terminology.hl7.org/CodeSystem/data-absent-reason| Code | Display | Definition |
| not-applicable | Not Applicable | There is no proper value for this element (e.g. last menstrual period for a male). |
- Include these codes as defined in
http://hl7.org/fhir/sid/icd-10| Code | Display |
| D61.0 | Constitutional aplastic anemia |
| D82.0 | Wiskott-Aldrich syndrome |
| D82.3 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| E34.8 | Other specified endocrine disorders |
| G11.3 | Cerebellar ataxia with defective DNA repair |
| K86.1 | Other chronic pancreatitis |
| L72.8 | Other follicular cysts of the skin and subcutaneous tissue |
| Q78.6 | Multiple congenital exostoses |
| Q82.1 | Xeroderma pigmentosum |
| Q82.2 | Congenital cutaneous mastocytosis |
| Q82.8 | Other specified congenital malformations of skin |
| Q85.0 | Neurofibromatosis (nonmalignant) |
| Q85.1 | Tuberous sclerosis |
| Q85.8 | Other phakomatoses, not elsewhere classified |
| Q87.3 | Congenital malformation syndromes involving early overgrowth |
| Q87.8 | Other specified congenital malformation syndromes, not elsewhere classified |
Source
{
"resourceType": "ValueSet",
"id": "vs-icd10-predisposition-eu-pcsp",
"text": {
"status": "extensions",
"div": "<!-- snip (see above) -->"
},
"url": "http://hl7.eu/fhir/ig/pcsp/ValueSet/vs-icd10-predisposition-eu-pcsp",
"version": "0.1.0",
"name": "ICD10HereditaryPredisposition",
"title": "Hereditary Predispositions (ICD10)",
"status": "active",
"experimental": false,
"date": "2023-01-26T09:50:21+01:00",
"publisher": "PanCareSurPass Project",
"contact": [
{
"name": "PanCareSurPass Project",
"telecom": [
{
"system": "url",
"value": "https://www.pancaresurpass.eu/"
}
]
},
{
"name": "PanCareSurPass Project",
"telecom": [
{
"system": "url",
"value": "https://www.pancaresurpass.eu/"
}
]
}
],
"description": "Hereditary Predispositions (ICD10)",
"jurisdiction": [
{
"coding": [
{
"system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code": "150",
"display": "Europe"
}
]
}
],
"compose": {
"include": [
{
"system": "http://terminology.hl7.org/CodeSystem/data-absent-reason",
"concept": [
{
"code": "not-applicable"
}
]
},
{
"system": "http://hl7.org/fhir/sid/icd-10",
"concept": [
{
"code": "D61.0",
"display": "Constitutional aplastic anemia"
},
{
"code": "D82.0",
"display": "Wiskott-Aldrich syndrome"
},
{
"code": "D82.3",
"display": "Immunodeficiency following hereditary defective response to Epstein-Barr virus"
},
{
"code": "E34.8",
"display": "Other specified endocrine disorders"
},
{
"code": "G11.3",
"display": "Cerebellar ataxia with defective DNA repair"
},
{
"code": "K86.1",
"display": "Other chronic pancreatitis"
},
{
"code": "L72.8",
"display": "Other follicular cysts of the skin and subcutaneous tissue"
},
{
"code": "Q78.6",
"display": "Multiple congenital exostoses"
},
{
"code": "Q82.1",
"display": "Xeroderma pigmentosum"
},
{
"code": "Q82.2",
"display": "Congenital cutaneous mastocytosis"
},
{
"code": "Q82.8",
"display": "Other specified congenital malformations of skin"
},
{
"code": "Q85.0",
"display": "Neurofibromatosis (nonmalignant)"
},
{
"code": "Q85.1",
"display": "Tuberous sclerosis"
},
{
"code": "Q85.8",
"display": "Other phakomatoses, not elsewhere classified"
},
{
"code": "Q87.3",
"display": "Congenital malformation syndromes involving early overgrowth"
},
{
"code": "Q87.8",
"display": "Other specified congenital malformation syndromes, not elsewhere classified"
}
]
}
]
}
}
FHIR