XpanDH Patient Summary
0.1.0 - ci-build
150
XpanDH Patient Summary, published by XpanDH Project. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/xpandh-ps/ and changes regularly. See the Directory of published versions
Active as of 2024-12-12 |
{
"resourceType" : "ValueSet",
"id" : "eHDSIRareDisease",
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet eHDSIRareDisease</b></p><a name=\"eHDSIRareDisease\"> </a><a name=\"hceHDSIRareDisease\"> </a><a name=\"eHDSIRareDisease-en-US\"> </a><ul><li>Include these codes as defined in <code>https://www.orpha.net</code><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td>5</td><td>Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency</td></tr><tr><td>6</td><td>3-methylcrotonyl-CoA carboxylase deficiency</td></tr><tr><td>7</td><td>3C syndrome</td></tr></table></li></ul></div>"
},
"url" : "http://terminology.ehdsi.eu/ValueSet/eHDSIRareDisease",
"version" : "0.1.0",
"name" : "EHDSIRareDisease",
"title" : "Rare Disease (PARTIAL)",
"status" : "active",
"experimental" : false,
"date" : "2024-12-12T10:23:54+00:00",
"publisher" : "XpanDH Project",
"contact" : [
{
"name" : "XpanDH Project",
"telecom" : [
{
"system" : "url",
"value" : "https://xpandh-project.iscte-iul.pt"
}
]
}
],
"description" : "The Value Set is used to describe the problems and medication reasons.",
"jurisdiction" : [
{
"coding" : [
{
"system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code" : "150",
"display" : "Europe"
}
]
}
],
"copyright" : "Used by permission of the XpanDH project, all rights reserved Creative Commons License",
"compose" : {
"include" : [
{
"system" : "https://www.orpha.net",
"concept" : [
{
"code" : "5",
"display" : "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency"
},
{
"code" : "6",
"display" : "3-methylcrotonyl-CoA carboxylase deficiency"
},
{
"code" : "7",
"display" : "3C syndrome"
}
]
}
]
}
}