85951000119104: enkelvoudige congenitale afwijking in familieanamnese (situatie)

SNOMED CT Concept\Situation with explicit context (situation)\...

\Finding with explicit context (situation)\Family history of clinical finding\Family history of disorder\...

\Family history of development disorder\Family history of congenital malformation\Family history of single congenital anomaly

\Family history of congenital disease (situation)\Family history of congenital malformation\Family history of single congenital anomaly

\Family history with explicit context (situation)\Family history of clinical finding\Family history of disorder\...

\Family history of development disorder\Family history of congenital malformation\Family history of single congenital anomaly

\Family history of congenital disease (situation)\Family history of congenital malformation\Family history of single congenital anomaly

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3076152012 Family history of single congenital anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3076184017 Family history of single congenital anomaly (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

11259151000146114 enkelvoudige congenitale afwijking in familieanamnese (situatie) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

11561711000146112 solitaire congenitale misvorming in familieanamnese nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

11561721000146119 enkelvoudige congenitale afwijking in familieanamnese nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Family history of single congenital anomaly	Is a	Family history of congenital disease (situation)	false	Inferred relationship	Some
Family history of single congenital anomaly	Associated finding	Congenital malformation	true	Inferred relationship	Some	1
Family history of single congenital anomaly	Subject relationship context (attribute)	persoon in familie van zorgafnemer	false	Inferred relationship	Some	1
Family history of single congenital anomaly	Temporal context (attribute)	Current or past (actual) (qualifier value)	true	Inferred relationship	Some	1
Family history of single congenital anomaly	Finding context (attribute)	Known present (qualifier value)	true	Inferred relationship	Some	1
Family history of single congenital anomaly	Is a	Family history of development disorder	false	Inferred relationship	Some
Family history of single congenital anomaly	Subject relationship context (attribute)	Person in the family (person)	true	Inferred relationship	Some	1
Family history of single congenital anomaly	Is a	Family history of congenital malformation	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets