702575003: Retinocochleocerebral vasculopathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Cardiovascular finding\Disorder of cardiovascular system\Cerebrovascular disease (disorder)\An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.

\Disease\Disorder of immune function (disorder)\Autoimmune disease\An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.
\Disease\Disorder of body system\Disorder of cardiovascular system\Cerebrovascular disease (disorder)\An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.

Status: current, 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

3004406019 Susac syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3004432013 Retinocochleocerebral vasculopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3004502015 Retinocochleocerebral vasculopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3010217016 An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3010219018 An arteriopathy characterised by visual loss, progressive or episodic deafness, and abnormal fundoscopy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3004406019 Susac syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3004432013 Retinocochleocerebral vasculopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3004432013 Retinocochleocerebral vasculopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3004502015 Retinocochleocerebral vasculopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3004502015 Retinocochleocerebral vasculopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3010217016 An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3010219018 An arteriopathy characterised by visual loss, progressive or episodic deafness, and abnormal fundoscopy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3391281001000114 Susac-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

614831000172114 vasculopathie rétinocochléocérébrale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

614831000172114 vasculopathie rétinocochléocérébrale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3391281001000114 Susac-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.	Is a	Cerebrovascular disease (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.	Is a	Autoimmune disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.	Finding site	Cerebrovascular system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy.	Pathological process (attribute)	Autoimmune process	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships

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This concept is not in any reference sets