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237867001: Hereditary cerebrovascular amyloidosis (disorder)

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
356475019 Hereditary cerebrovascular amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5020761000241114 amylose cérébrovasculaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary cerebrovascular amyloidosis (disorder) Is a Cerebrovascular amyloidosis false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Finding site Cerebrovascular system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebrovascular amyloidosis (disorder) Finding site Cardiovascular system subdivision false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Associated morphology Focal amyloid false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebrovascular amyloidosis (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Finding site Cerebrovascular system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebrovascular amyloidosis (disorder) Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebrovascular amyloidosis (disorder) Is a Hereditary amyloidosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebrovascular amyloidosis (disorder) Is a Cerebral amyloid angiopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary cerebral hemorrhage with amyloidosis (disorder) Is a True Hereditary cerebrovascular amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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