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721141004: Hereditary vascular retinopathy (disorder)

Status: retired, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3323683018 Hereditary vascular retinopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3323684012 Hereditary vascular retinopathy en Synonym Active Case insensitive SNOMED CT core

3323685013 A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy and characterized by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms. en Definition Active Case sensitive SNOMED CT core

3323686014 A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leucodystrophy and characterised by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary vascular retinopathy	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
Hereditary vascular retinopathy	Is a	Retinal vascular disorder	false	Inferred relationship	Some
Hereditary vascular retinopathy	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Some
Hereditary vascular retinopathy	Is a	Hereditary disorder of the visual system	false	Inferred relationship	Some
Hereditary vascular retinopathy	Finding site	Structure of blood vessel of retina	false	Inferred relationship	Some

Inbound Relationships

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Active

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Characteristic

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Group

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3323683018	Hereditary vascular retinopathy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3323684012	Hereditary vascular retinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
3323685013	A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy and characterized by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms.	en	Definition	Active	Case sensitive	SNOMED CT core
3323686014	A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leucodystrophy and characterised by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms.	en	Definition	Active	Case sensitive	SNOMED CT core