ID

44025

Description

Derived from www.openehr.org Use to record information about the prevalence of an identified risk factor, problem or diagnosis in genetic and non-genetic family members. This archetype has specifically been designed to be used in the 'Detail' SLOT within the EVALUATION.health_risk archetype to support assessment of risk in the subject of care for the identified 'Risk factor' and the 'Family prevalence' SLOT in the EVALUATION.family_history archetype. It can also be used in the 'Specific details' SLOT within the EVALUATION.problem_diagnosis archetype ,or other EVALUATION or CLUSTER archetypes, where clinically appropriate.

Lien

www.openehr.org

Mots-clés

Versions (3)
  1. 08/07/2017 08/07/2017 - Martin Dugas
  2. 08/07/2017 08/07/2017 - Martin Dugas
  3. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-SA 3.0
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Family prevalence (EHR archetype)

Anglais

openEHR-EHR-CLUSTER.family_prevalence.v1

1 Formulaires  
  1. StudyEvent: openEHR-EHR-CLUSTER.family_prevalence.v1
    1. openEHR-EHR-CLUSTER.family_prevalence.v1
openEHR-EHR-CLUSTER.family_prevalence.v1.xml
Description

openEHR-EHR-CLUSTER.family_prevalence.v1.xml

Family prevalence
Description

Summary information about the prevalence of a risk factor, problem or diagnosis in all family members.

Type de données

text

Description
Description

Narrative description about occurrence in family members.

Type de données

text

Affected family
Description

Details about the numbers of family members affected.

Type de données

text

Relationship
Description

The degree of relationship between the subject of care and a selected group of family members.

Type de données

text

Biological sex
Description

The biological sex of the family member/s.

Type de données

text

Alias
UMLS CUI [1]
C0079399
Number affected
Description

The number of family members known to be affected.

Type de données

integer

Family line
Description

Identification of the maternal or paternal family line in the relationship.

Type de données

text

Number eligible
Description

The number of eligible family members.

Type de données

integer

Genetic predisposition?
Description

Is there a genetic basis for the identified risk factor, problem or diagnosis?

Type de données

boolean

Alias
UMLS CUI [1]
C0314657
Inheritance type
Description

Category of inheritance for the identified identified risk factor, problem or diagnosis.

Type de données

text

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Similar models

openEHR-EHR-CLUSTER.family_prevalence.v1

1 Formulaires
  1. StudyEvent: openEHR-EHR-CLUSTER.family_prevalence.v1
    1. openEHR-EHR-CLUSTER.family_prevalence.v1
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Family prevalence
Item
Family prevalence
text
Description
Item
Description
text
Affected family
Item
Affected family
text
Item
Relationship
text
Relationship
Code List
Relationship
CL Item
First degree relative (1)
CL Item
Second degree relative (2)
CL Item
Third degree relative (3)
CL Item
Genetic family (4)
CL Item
Non-genetic family (5)
Item
Biological sex
text
C0079399 (UMLS CUI [1])
Biological sex
Code List
Biological sex
CL Item
Male (1)
C0086582 (UMLS CUI-1)
CL Item
Female (2)
C0086287 (UMLS CUI-1)
CL Item
Indeterminate/Intersex/Unspecified (3)
C0205258 (UMLS CUI-1)
Number affected
Item
Number affected
integer
Item
Family line
text
Family line
Code List
Family line
CL Item
Maternal line (1)
CL Item
Paternal line (2)
Number eligible
Item
Number eligible
integer
Genetic predisposition
Item
Genetic predisposition?
boolean
C0314657 (UMLS CUI [1])
Inheritance type
Item
Inheritance type
text
Retour au début de la page 

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