205998002: [X]Sex chromosome abnormality, male phenotype, unspecified (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

315808018 [X]Sex chromosome abnormality, male phenotype, unspecified en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591439018 [X]Sex chromosome abnormality, male phenotype, unspecified (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

315808018 [X]Sex chromosome abnormality, male phenotype, unspecified en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

315808018 [X]Sex chromosome abnormality, male phenotype, unspecified en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591439018 [X]Sex chromosome abnormality, male phenotype, unspecified (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591439018 [X]Sex chromosome abnormality, male phenotype, unspecified (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

591439018 [X]Sex chromosome abnormality, male phenotype, unspecified (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
[X]Sex chromosome abnormality, male phenotype, unspecified	Is a	Sex chromosome abnormality - male phenotype	false	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Sex chromosome abnormality, male phenotype, unspecified	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Sex chromosome abnormality, male phenotype, unspecified	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
[X]Sex chromosome abnormality, male phenotype, unspecified	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Sex chromosome abnormality, male phenotype, unspecified	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
[X]Sex chromosome abnormality, male phenotype, unspecified	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
[X]Sex chromosome abnormality, male phenotype, unspecified	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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

MOVED TO association reference set