190511001: Congenital adrenogenital syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

292789016 Congenital adrenogenital syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

574099017 Congenital adrenogenital syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

292789016 Congenital adrenogenital syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

292789016 Congenital adrenogenital syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

292790013 Congenital adrenal cortical hyperplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

574099017 Congenital adrenogenital syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

574099017 Congenital adrenogenital syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

76191000077116 hyperplasie corticosurrénale congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

76191000077116 hyperplasie corticosurrénale congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
hyperplasie corticosurrénale congénitale	Is a	Adrenogenital disorder (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
hyperplasie corticosurrénale congénitale	Finding site	Adrenal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
hyperplasie corticosurrénale congénitale	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
hyperplasie corticosurrénale congénitale	Is a	Congenital disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
hyperplasie corticosurrénale congénitale	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Feminization-adrenogenital syndrome	Is a	False	hyperplasie corticosurrénale congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Virilisation-adrenogenital syndrome	Is a	False	hyperplasie corticosurrénale congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)