720854004: Cerebroretinal vasculopathy (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module	Reference Sets
3322297012	Cerebroretinal vasculopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
3322298019	Cerebroretinal vasculopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
3322299010	Grand Kaine Fulling syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
3322300019	A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy characterized by strokes, vision loss, migraines, pseudotumors, dementia and occasionally renal disease.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
3322301015	A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leucodystrophy characterised by strokes, vision loss, migraines, pseudotumours, dementia and occasionally renal disease.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
3891801000052111	cerebroretinal vaskulopati	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)	Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
cerebroretinal vaskulopati	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
cerebroretinal vaskulopati	Is a	Retinal vascular disorder (disorder)	false	Inferred relationship	Some
cerebroretinal vaskulopati	Is a	Cerebrovascular disease	false	Inferred relationship	Some
cerebroretinal vaskulopati	Is a	Leucodystrophy	false	Inferred relationship	Some
cerebroretinal vaskulopati	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Some
cerebroretinal vaskulopati	Is a	Hereditary disorder of the visual system (disorder)	false	Inferred relationship	Some
cerebroretinal vaskulopati	Finding site	Cerebrovascular system structure	false	Inferred relationship	Some
cerebroretinal vaskulopati	Finding site	Structure of blood vessel of retina (body structure)	false	Inferred relationship	Some
cerebroretinal vaskulopati	Associated morphology	Dystrophy	false	Inferred relationship	Some	3
cerebroretinal vaskulopati	Associated morphology	Myelin sheath alteration	false	Inferred relationship	Some	3
cerebroretinal vaskulopati	Finding site	Structure of nervous system (body structure)	false	Inferred relationship	Some	3
cerebroretinal vaskulopati	Associated morphology	Dystrophy	false	Inferred relationship	Some	2
cerebroretinal vaskulopati	Finding site	Myelinated nerve fiber structure	false	Inferred relationship	Some	1
cerebroretinal vaskulopati	Finding site	White matter structure of brain and spinal cord (body structure)	false	Inferred relationship	Some	2
cerebroretinal vaskulopati	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
cerebroretinal vaskulopati	Associated morphology	Myelin sheath alteration	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)