ID

44025

Beskrivning

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.

Länk

www.openehr.org

Nyckelord

Versioner (3)
  1. 2017-07-08 2017-07-08 - Martin Dugas
  2. 2017-07-08 2017-07-08 - Martin Dugas
  3. 2021-09-20 2021-09-20 -
Uppladdad den

20 september 2021

DOI

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Licens

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

Engelsk

openEHR-EHR-CLUSTER.family_prevalence.v1

1 Formulär  
  1. StudyEvent: openEHR-EHR-CLUSTER.family_prevalence.v1
    1. openEHR-EHR-CLUSTER.family_prevalence.v1
openEHR-EHR-CLUSTER.family_prevalence.v1.xml
Beskrivning

openEHR-EHR-CLUSTER.family_prevalence.v1.xml

Family prevalence
Beskrivning

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

Datatyp

text

Description
Beskrivning

Narrative description about occurrence in family members.

Datatyp

text

Affected family
Beskrivning

Details about the numbers of family members affected.

Datatyp

text

Relationship
Beskrivning

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

Datatyp

text

Biological sex
Beskrivning

The biological sex of the family member/s.

Datatyp

text

Alias
UMLS CUI [1]
C0079399
Number affected
Beskrivning

The number of family members known to be affected.

Datatyp

integer

Family line
Beskrivning

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

Datatyp

text

Number eligible
Beskrivning

The number of eligible family members.

Datatyp

integer

Genetic predisposition?
Beskrivning

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

Datatyp

boolean

Alias
UMLS CUI [1]
C0314657
Inheritance type
Beskrivning

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

Datatyp

text

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Similar models

openEHR-EHR-CLUSTER.family_prevalence.v1

1 Formulär
  1. StudyEvent: openEHR-EHR-CLUSTER.family_prevalence.v1
    1. openEHR-EHR-CLUSTER.family_prevalence.v1
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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
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