43532007: Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

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

\Central nervous system finding\Finding of meninges (finding)\Disorder of meninges\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of meninges\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis (disorder)\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of meninges\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
\Disease\Amyloidosis\Hereditary amyloidosis (disorder)\Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Localized amyloidosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Disorder of blood vessel (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Disorder of meninges	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Finding site	Blood vessel structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Finding site	Leptomeninges structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Associated morphology	Focal amyloid	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Hereditary amyloidosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Is a	Hereditary degenerative disease of central nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Causative agent (attribute)	Transthyretin (substance)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	Associated morphology	Amyloid deposition	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
72596012	Hereditary oculoleptomeningeal amyloid angiopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
72597015	Amyloidosis VII	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
72598013	Ohio type amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
493631014	Familial oculoleptomeningeal amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
780556017	Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
72596012	Hereditary oculoleptomeningeal amyloid angiopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
72596012	Hereditary oculoleptomeningeal amyloid angiopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
72597015	Amyloidosis VII	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
72598013	Ohio type amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
493631014	Familial oculoleptomeningeal amyloidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
493631014	Familial oculoleptomeningeal amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
780556017	Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
780556017	Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5999401000241114	amyloïdose VII	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5999421000241116	angiopathie amyloïde oculoleptoméningée héréditaire à la transthyrétine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5999431000241119	amyloïde oculoleptoméningée familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5999401000241114	amyloïdose VII	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5999421000241116	angiopathie amyloïde oculoleptoméningée héréditaire à la transthyrétine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5999431000241119	amyloïde oculoleptoméningée familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module