43532007: Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

SNOMED CT Concept\Clinical 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\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 of meninges\Hereditary oculoleptomeningeal amyloid angiopathy

\Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis\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\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\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 of the central nervous system\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 of the central nervous system\Disorder of meninges\Hereditary oculoleptomeningeal amyloid angiopathy

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

Descriptions:

Id Description Lang Type Status Case? Module

72596012 Hereditary oculoleptomeningeal amyloid angiopathy en Synonym Active Entire term case insensitive SNOMED CT core module

72597015 Amyloidosis VII en Synonym Active Only initial character case insensitive SNOMED CT core module

72598013 Ohio type amyloidosis en Synonym Active Entire term case sensitive SNOMED CT core module

493631014 Familial oculoleptomeningeal amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module

780556017 Hereditary oculoleptomeningeal amyloid angiopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Localized amyloidosis	false	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Disorder of blood vessel	false	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Disorder of meninges	true	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Finding site	Blood vessel structure	false	Inferred relationship	Existential restriction modifier	3
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Finding site	Leptomeninges structure	true	Inferred relationship	Existential restriction modifier	1
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	Focal amyloid	false	Inferred relationship	Existential restriction modifier	2
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Hereditary amyloidosis	true	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Is a	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy	Causative agent	Prealbumin	true	Inferred relationship	Existential restriction modifier	1
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	Amyloid deposition	true	Inferred relationship	Existential restriction modifier	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	Active	Entire term case insensitive	SNOMED CT core module
72597015	Amyloidosis VII	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
72598013	Ohio type amyloidosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
493631014	Familial oculoleptomeningeal amyloidosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
780556017	Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module