26133007: Congenital atrophy (morphologic abnormality)

Status: retired, Not 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

43787010 Congenital atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

756530014 Congenital atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

43787010 Congenital atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

43787010 Congenital atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

756530014 Congenital atrophy (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

756530014 Congenital atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital atrophy	Is a	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy	Is a	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial febrile convulsions	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital cerebellar cortical atrophy	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of kidney	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital ischaemic atrophy of central nervous system structure	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital cerebellar cortical atrophy (disorder)	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of thyroid	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital renal atrophy	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital renal atrophy	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of thyroid	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital cerebellar cortical atrophy (disorder)	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial febrile convulsions	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital cerebellar cortical atrophy (disorder)	Associated morphology	False	Congenital atrophy	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Reference Sets

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

SAME AS association reference set (foundation metadata concept)