237867001: Hereditary cerebrovascular amyloidosis (disorder)

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

\Cardiovascular finding\Disorder of cardiovascular system (disorder)\...

\Cardiovascular system hereditary disorder\Hereditary cerebrovascular amyloidosis

\Cerebrovascular disease\Cerebral amyloid angiopathy\Hereditary cerebrovascular amyloidosis

\Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis (disorder)\Hereditary cerebrovascular amyloidosis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Hereditary cerebrovascular amyloidosis
\Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Hereditary cerebrovascular amyloidosis
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Hereditary cerebrovascular amyloidosis
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cerebrovascular disease\Cerebral amyloid angiopathy\Hereditary cerebrovascular amyloidosis
\Disease\Amyloidosis\Hereditary amyloidosis (disorder)\Hereditary cerebrovascular amyloidosis
\Disease\Amyloidosis\Cerebral amyloid angiopathy\Hereditary cerebrovascular amyloidosis

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

356475019 Hereditary cerebrovascular amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626657019 Hereditary cerebrovascular amyloidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5020761000241114 amylose cérébrovasculaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary cerebrovascular amyloidosis	Is a	Cerebrovascular amyloidosis	false	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Finding site	Blood vessel structure (body structure)	false	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Finding site	Cerebrovascular system structure	false	Inferred relationship	Some	1
Hereditary cerebrovascular amyloidosis	Finding site	Structure of cardiovascular system subdivision (body structure)	false	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Associated morphology	Amyloid deposition	false	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Associated morphology	Focal amyloid	false	Inferred relationship	Some	1
Hereditary cerebrovascular amyloidosis	Finding site	Brain structure	false	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Finding site	Cerebrovascular system structure	true	Inferred relationship	Some	1
Hereditary cerebrovascular amyloidosis	Associated morphology	Focal amyloid	true	Inferred relationship	Some	1
Hereditary cerebrovascular amyloidosis	Is a	Hereditary amyloidosis (disorder)	true	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Is a	Cardiovascular system hereditary disorder	true	Inferred relationship	Some
Hereditary cerebrovascular amyloidosis	Is a	Cerebral amyloid angiopathy	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare genetic cerebral small vessel disease characterized by amyloid deposition in the cerebral blood vessels leading to predominantly hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.	Is a	True	Hereditary cerebrovascular amyloidosis	Inferred relationship	Some

This concept is not in any reference sets