64991000119107: Family history of velocardiofacial syndrome (situation)

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 multiple congenital anomalies (situation)\Family history of velocardiofacial syndrome (situation)

\Family history of congenital disease (situation)\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of velocardiofacial syndrome (situation)
\Family history of congenital disease (situation)\Family history of chromosomal anomaly (situation)\Family history of velocardiofacial syndrome (situation)

\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 multiple congenital anomalies (situation)\Family history of velocardiofacial syndrome (situation)

\Family history of congenital disease (situation)\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of velocardiofacial syndrome (situation)
\Family history of congenital disease (situation)\Family history of chromosomal anomaly (situation)\Family history of velocardiofacial syndrome (situation)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2017. Module: US National Library of Medicine maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

740811000124112 Family history of velocardiofacial syndrome (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)

740821000124116 Family history of velocardiofacial syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Family history of velocardiofacial syndrome (situation)	Is a	Family history of congenital disease (situation)	false	Inferred relationship	Some
Family history of velocardiofacial syndrome (situation)	Associated finding	Shprintzen syndrome	false	Inferred relationship	Some	1
Family history of velocardiofacial syndrome (situation)	Subject relationship context (attribute)	Person in family of subject	false	Inferred relationship	Some	1
Family history of velocardiofacial syndrome (situation)	Temporal context (attribute)	Current or past (actual) (qualifier value)	true	Inferred relationship	Some	1
Family history of velocardiofacial syndrome (situation)	Finding context (attribute)	Known present (qualifier value)	true	Inferred relationship	Some	1
Family history of velocardiofacial syndrome (situation)	Is a	Family history of multiple congenital anomalies (situation)	true	Inferred relationship	Some
Family history of velocardiofacial syndrome (situation)	Is a	Family history of chromosomal anomaly (situation)	true	Inferred relationship	Some
Family history of velocardiofacial syndrome (situation)	Associated finding	22q11.2 deletion syndrome (disorder)	true	Inferred relationship	Some	1
Family history of velocardiofacial syndrome (situation)	Subject relationship context (attribute)	Person in the family (person)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets