fr-cda-batterie-examens-de-biologie-medicale
type: StructureDefinition
node role: treeRoot
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    v: Narratif généré : DéfinitionStructure fr-cda-batterie-examens-de-biologie-medicale Nom Drapeaux Card. Type Description et contraintes<img src="[binary]" alt="doco" style="background-color: inherit"/> Organizer 1..1 Organizer Espace de noms (namespace) XML: urn:hl7-org:v3 Base for all types and resources Les instances de ce type sont validées par templateId Conteneur logique: ClinicalDocument (CDA Class) #xD; Slices pour templateId 2..2 II Slice: Non ordonné, Ouvert par value:root #xD; templateId:iheLaboratoryBatteryOrganizer 1..1 II Conformité Laboratory Battery Organizer (IHE PaLM) #xD; @root 1..1 oid, uuid, ruid Motif requis: 1.3.6.1.4.1.19376.1.3.1.4 #xD; templateId:frBatterieExamensDeBiologieMedicale 1..1 II Conformité FR-Batterie-examens-de-biologie-medicale (CI-SIS) #xD; @root 1..1 oid, uuid, ruid Motif requis: 1.2.250.1.213.1.1.3.78 #xD; @classCode S 1..1 cs Motif requis: BATTERY #xD; @moodCode S 1..1 cs #xD; id S 0..1 II Identifiant de l'entrée #xD; code S 0..1 CD Code de la batterie d'examen #xD; @code S 1..1 cs #xD; @codeSystem S 1..1 oid, uuid, ruid #xD; @displayName S 0..1 st #xD; originalText S 0..1 ED #xD; reference 1..1 TEL Référence à l'expression verbale dans la partie visualisable du compte-rendu #xD; translation 0..1 CD Code d'identification d'attente national ou code de portée locale #xD; statusCode S 1..1 CS Niveau de complétude Binding: ActStatus (required) #xD; effectiveTime S 0..1 IVL_TS Date de l'examen #xD; subject S 0..1 FRCDASujetNonHumain, FRCDAPatientAvecSujetNonHumain Sujet non humain - Cet élément doit être présent lorsque le sujet des observations est un échantillon provenant d'un sujet non humain (animal ou autre élément environnemental). Le sujet non humain doit aussi être décrit dans l'en-tête du document. Participant avec sujet non humain - Cet élément doit être présent lorsque le sujet des observations de cette partie du compte rendu est un échantillon provenant d'un sujet non humain (animal ou autre élément environnemental), ta…
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  l: fr-cda-batterie-examens-de-biologie-medicale
version:
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name:
  v: FRCDABatterieExamensDeBiologieMedicale
title:
  v: CDA - FR Batterie examens de biologie medicale
status:
  v: draft
date:
  v: 2026-04-24T12:43:17+00:00
publisher:
  v: Agence du Numérique en Santé (ANS) - 2-10 Rue d'Oradour-sur-Glane, 75015 Paris
contact:
  name:
    v: Agence du Numérique en Santé (ANS) - 2-10 Rue d'Oradour-sur-Glane, 75015 Paris
  telecom:
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      v: url
    value:
      v: https://esante.gouv.fr
description:
  v: Entrée FR-Batterie-examens-de-biologie-medicale: IHE-PCC - Laboratory Battery Organizer. L'entrée Batterie d'examens de biologie médicale est une entrée de type 'organizer' qui permet de décrire des examens de biologie médicale comprenant un ou plusieurs éléments porteurs de résultats et d'éventuels commentaires interprétant cet ensemble de résultats. L'examen de biologie médicale peut préciser des participants qui lui sont propres (validateur, auteur, responsable, laboratoire sous-traitant, automate …) et peut aussi décrire son échantillon biologique.
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  v: If a value is an exceptional value (NULL-value), this specifies in what way and why proper information is missing.
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  v: The integrity check is a short binary value representing a cryptographically strong checksum that is calculated over the binary data. The purpose of this property, when communicated with a reference is for anyone to validate later whether the reference still resolved to the same data that the reference resolved to when the encapsulated data value with reference was created.
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  v: Data that is primarily intended for human interpretation or for further machine processing is outside the scope of HL7. This includes unformatted or formatted written language, multimedia data, or structured information as defined by a different standard (e.g., XML-signatures.)
comment:
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  v: Référence à l'expression verbale dans la partie visualisable du compte-rendu
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  v: Sujet non humain - Cet élément doit être présent lorsque le sujet des observations est un échantillon provenant d'un sujet non humain (animal ou autre élément environnemental). Le sujet non humain doit aussi être décrit dans l'en-tête du document. Participant avec sujet non humain - Cet élément doit être présent lorsque le sujet des observations de cette partie du compte rendu est un échantillon provenant d'un sujet non humain (animal ou autre élément environnemental), tandis que les autres parties du rapport sont liés au patient humain. Le sujet non humain doit aussi être décrit dans l'en-tête du document.
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id:
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must support:
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id:
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id:
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id:
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id:
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  v: A human readable name or mnemonic for the assigning authority. The Assigning Authority Name has no computational value. The purpose of a Assigning Authority Name is to assist an unaided human interpreter of an II value to interpret the authority. Note: no automated processing must depend on the assigning authority name to be present in any form.
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id:
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id:
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id:
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  v: A human readable name or mnemonic for the assigning authority. The Assigning Authority Name has no computational value. The purpose of a Assigning Authority Name is to assist an unaided human interpreter of an II value to interpret the authority. Note: no automated processing must depend on the assigning authority name to be present in any form.
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id:
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definition:
  v: When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question
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type:
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default value: Code
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id:
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element:
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  short:
    v: Sujet non humain - Cet élément doit être présent lorsque le sujet des observations est un échantillon provenant d'un sujet non humain (animal ou autre élément environnemental). Le sujet non humain doit aussi être décrit dans l'en-tête du document. Participant avec sujet non humain - Cet élément doit être présent lorsque le sujet des observations de cette partie du compte rendu est un échantillon provenant d'un sujet non humain (animal ou autre élément environnemental), tandis que les autres parties du rapport sont liés au patient humain. Le sujet non humain doit aussi être décrit dans l'en-tête du document.
  definition:
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v: true

id:
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path:
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short:
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definition:
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type:
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id:
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path:
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short:
  v: Auteur - Apparaît à ce niveau si le rendu de ce résultat procède de cet auteur spécifique, différent de celui déclaré aux niveaux supérieurs. Constraint @typeCode='AUT'
type:
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id:
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path:
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short:
  v: Participant - Les attributs de cet élément prennent les valeurs suivantes : @typeCode= 'AUTHEN' pour 'Valideur de ces résultats' @typeCode='RESP' pour 'Responsable de cet examen' @typeCode='DEV' pour 'Dispositif automatique impliqué dans la production des résultats'
definition:
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