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703220002: Hereditary cystatin C amyloid angiopathy (disorder)

Status: retired, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3007478010 Hereditary cystatin C amyloid angiopathy (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

3007920011 Hereditary cystatin C amyloid angiopathy en Synonym Active Initial character case insensitive SNOMED CT core

3008060012 A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral haemorrhage and dementia and is inherited in a dominant pattern. en Definition Active Case sensitive SNOMED CT core

3008067010 A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral hemorrhage and dementia and is inherited in a dominant pattern. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary cystatin C amyloid angiopathy	Is a	Hereditary amyloidosis	false	Inferred relationship	Some
Hereditary cystatin C amyloid angiopathy	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
Hereditary cystatin C amyloid angiopathy	Is a	Cerebral amyloid angiopathy	false	Inferred relationship	Some
Hereditary cystatin C amyloid angiopathy	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Hereditary cystatin C amyloid angiopathy	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Some
Hereditary cystatin C amyloid angiopathy	Associated morphology	Amyloid deposition	false	Inferred relationship	Some	1
Hereditary cystatin C amyloid angiopathy	Finding site	Cerebrovascular system structure	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3007478010	Hereditary cystatin C amyloid angiopathy (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3007920011	Hereditary cystatin C amyloid angiopathy	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3008060012	A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral haemorrhage and dementia and is inherited in a dominant pattern.	en	Definition	Active	Case sensitive	SNOMED CT core
3008067010	A rare fatal amyloid disease in young people caused by a mutation in cystatin C. This condition predisposes towards intracerebral hemorrhage and dementia and is inherited in a dominant pattern.	en	Definition	Active	Case sensitive	SNOMED CT core