43532007: Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

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

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

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

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	Is a	Localized amyloidosis	false	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Vascular disorder	false	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Disorder of meninges	true	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Finding site	Blood vessel structure (body structure)	false	Inferred relationship	Some	3
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	Amyloid deposition	false	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Finding site	Leptomeninges structure	true	Inferred relationship	Some	1
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	Focal amyloid	false	Inferred relationship	Some	2
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Hereditary amyloidosis (disorder)	true	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Some
Hereditary oculoleptomeningeal amyloid angiopathy	Causative agent	Prealbumin	true	Inferred relationship	Some	1
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	Amyloid deposition	true	Inferred relationship	Some	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
11329461000172118	amyloïdose VII	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
11329471000172110	angiopathie amyloïde oculoleptoméningée héréditaire à la transthyrétine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
11329481000172113	amyloïde oculoleptoméningée familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5228951000172114	transthyretineamyloïdose	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5228961000172111	ATTR-amyloïdose	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)