700191004: Family history of congenital hip dysplasia (situation)

SNOMED CT Concept\Context-dependent categories\...

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

\Family history of development disorder\Family history of congenital malformation (situation)\FH: Cong. orthopedic anomaly\Family history of congenital hip dysplasia (situation)

\Family history: Musculoskeletal disease (situation)\FH: Cong. orthopedic anomaly\Family history of congenital hip dysplasia (situation)

\Family history of congenital disease (situation)\Family history of congenital malformation (situation)\FH: Cong. orthopedic anomaly\Family history of congenital hip dysplasia (situation)

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

\Family history of development disorder\Family history of congenital malformation (situation)\FH: Cong. orthopedic anomaly\Family history of congenital hip dysplasia (situation)

\Family history: Musculoskeletal disease (situation)\FH: Cong. orthopedic anomaly\Family history of congenital hip dysplasia (situation)

\Family history of congenital disease (situation)\Family history of congenital malformation (situation)\FH: Cong. orthopedic anomaly\Family history of congenital hip dysplasia (situation)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2989208010 Family history of congenital hip dysplasia (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2989513013 Family history of congenital hip dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2989208010 Family history of congenital hip dysplasia (situation) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2989208010 Family history of congenital hip dysplasia (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2989513013 Family history of congenital hip dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2989513013 Family history of congenital hip dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

358741000195113 famigliarità per displasia congenita dell'anca it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

358751000195111 anamnesi familiare di displasia congenita dell'anca it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6912811000241116 antécédent familial de dysplasie congénitale de la hanche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6912811000241116 antécédent familial de dysplasie congénitale de la hanche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

358741000195113 famigliarità per displasia congenita dell'anca it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

358751000195111 anamnesi familiare di displasia congenita dell'anca it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

22301001000119 Angeborene Hüftdysplasie in der Familienanamnese de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

22661001000111 Kongenitale Hüftdysplasie in der Familienanamnese de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Family history of congenital hip dysplasia (situation)	Is a	FH: Cong. orthopedic anomaly	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Family history of congenital hip dysplasia (situation)	Associated finding	Congenital hip dysplasia (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Family history of congenital hip dysplasia (situation)	Subject relationship context	Person in family of subject	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Family history of congenital hip dysplasia (situation)	Temporal context (attribute)	Current or past (actual) (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Family history of congenital hip dysplasia (situation)	Finding context	Known present (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Family history of congenital hip dysplasia (situation)	Is a	Family history of connective tissue disorder (situation)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Family history of congenital hip dysplasia (situation)	Subject relationship context	Person in the family	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets