URL | http://hl7.org/fhir/3.0/StructureDefinition/extension-Sequence.quality.truthFN |
Version | |
Status | active |
Description | Cross-Version Extension for Sequence.quality.truthFN. Valid in versions R2, R5 This is a valid cross-version extension because it's counted as a new element |
Context of Use
This extension may be used in the following contexts:
Name | Flags | Card. | Type | Description & Constraints![]() |
---|---|---|---|---|
![]() ![]() | 0..1 | Extension | False negatives | |
![]() ![]() ![]() | ..0 | |||
![]() ![]() ![]() | 1.. | decimal | ||
![]() ![]() ![]() | "http://hl7.org/fhir/3.0/StructureDefinition/extension-Sequence.quality.truthFN" | |||
![]() |
{ "resourceType" : "StructureDefinition", "id" : "xv-r3-seq.qua.truthFN", "url" : "http://hl7.org/fhir/3.0/StructureDefinition/extension-Sequence.quality.truthFN", "name" : "XVerExtensionSequence.quality.truthFNR3", "title" : "Cross-Version Extension for Sequence.quality.truthFN in R3", "status" : "active", "experimental" : false, "publisher" : "Health Level Seven International (Clinical Genomics)", "contact" : [{ "telecom" : [{ "system" : "url", "value" : "http://hl7.org/fhir" }] }, { "telecom" : [{ "system" : "url", "value" : "http://www.hl7.org/Special/committees/clingenomics/index.cfm" }] }], "description" : "Cross-Version Extension for Sequence.quality.truthFN. Valid in versions R2, R5\r\n\r\nThis is a valid cross-version extension because it's counted as a new element", "jurisdiction" : [{ "coding" : [{ "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm", "code" : "001" }] }], "fhirVersion" : "5.0.0", "kind" : "complex-type", "abstract" : false, "context" : [{ "type" : "extension", "expression" : "http://hl7.org/fhir/3.0/StructureDefinition/extension-Sequence.quality" }, { "type" : "extension", "expression" : "http://hl7.org/fhir/3.0/StructureDefinition/extension-Sequence.quality" }], "type" : "Extension", "baseDefinition" : "http://hl7.org/fhir/StructureDefinition/Extension", "derivation" : "constraint", "differential" : { "element" : [{ "path" : "Extension", "short" : "False negatives", "definition" : "False negatives, i.e. the number of sites in the Truth Call Set for which there is no path through the Query Call Set that is consistent with all of the alleles at this site, or sites for which there is an inaccurate genotype call for the event. Sites with correct variant but incorrect genotype are counted here.", "min" : 0, "max" : "1", "isModifier" : false }, { "path" : "Extension.extension", "max" : "0" }, { "path" : "Extension.value[x]", "min" : 1, "type" : [{ "code" : "decimal" }] }, { "path" : "Extension.url", "fixedUri" : "http://hl7.org/fhir/3.0/StructureDefinition/extension-Sequence.quality.truthFN" }] } }