95498007: Congenital myelin deficiency of the optic disc (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

158180014 Congenital myelin deficiency of the optic disc en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

839663015 Congenital myelin deficiency of the optic disc (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

158180014 Congenital myelin deficiency of the optic disc en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

158180014 Congenital myelin deficiency of the optic disc en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

839663015 Congenital myelin deficiency of the optic disc (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

839663015 Congenital myelin deficiency of the optic disc (disorder) 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 myelin deficiency of the optic disc	Is a	Congenital anomaly of optic disc	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital myelin deficiency of the optic disc	Finding site	Optic disc structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Associated morphology	Congenital deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital myelin deficiency of the optic disc	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital myelin deficiency of the optic disc	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital myelin deficiency of the optic disc	Finding site	Optic disc structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Associated morphology	Congenital deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Finding site	Optic disc structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital myelin deficiency of the optic disc	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital myelin deficiency of the optic disc	Finding site	Optic disc structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital myelin deficiency of the optic disc	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital myelin deficiency of the optic disc	Associated morphology	Morphologically abnormal structure	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)

REPLACED BY association reference set (foundation metadata concept)