716745004: Livedo reticularis and cerebrovascular accident syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\General finding of soft tissue\Blood vessel finding\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\General finding of soft tissue\Disorder of soft tissue\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome

\Cardiovascular finding\Cardiovascular disease\Cerebrovascular disease\Sneddon syndrome
\Cardiovascular finding\Cardiovascular disease\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\Cardiovascular finding\Blood vessel finding\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome

\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\Disease\Disorder of body system\Cardiovascular disease\Cerebrovascular disease\Sneddon syndrome
\Disease\Disorder of body system\Cardiovascular disease\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome
\Disease\Disorder of soft tissue\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Sneddon syndrome

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3307401018 Livedo reticularis and cerebrovascular accident syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3307402013 Livedo reticularis and cerebrovascular accident syndrome en Synonym Active Case insensitive SNOMED CT core

3307404014 Sneddon syndrome en Synonym Active Case sensitive SNOMED CT core

3307405010 Ehrmann Sneddon syndrome en Synonym Active Case sensitive SNOMED CT core

3307406011 Livedo racemosa and cerebrovascular accident en Synonym Active Case insensitive SNOMED CT core

3307407019 A rare non-inflammatory thrombotic vasculopathy predominantly affecting women in young adulthood. Livedo racemosa is a persistent net-like violaceous-cyanotic, mottled discoloration of the skin that is exacerbated by cold or pregnancy. Neurological manifestations include recurrent transient ischemic attacks and infarcts. While about 50% of cases are idiopathic, the disease can be associated with autoimmune diseases like systemic lupus erythematosus and antiphospholipid syndrome. Genetic factors may play a role in the pathogenesis. Loss-of-function mutations in cat eye syndrome chromosome region candidate 1 CECR1 (22q11.2) encoding adenosine deaminase 2 have been found. Most cases are sporadic but some familial cases with an autosomal dominant inheritance have been reported. en Definition Active Case sensitive SNOMED CT core

3307408012 A rare non-inflammatory thrombotic vasculopathy predominantly affecting women in young adulthood. Livedo racemosa is a persistent net-like violaceous-cyanotic, mottled discolouration of the skin that is exacerbated by cold or pregnancy. Neurological manifestations include recurrent transient ischaemic attacks and infarcts. While about 50% of cases are idiopathic, the disease can be associated with autoimmune diseases like systemic lupus erythematosus and antiphospholipid syndrome. Genetic factors may play a role in the pathogenesis. Loss-of-function mutations in cat eye syndrome chromosome region candidate 1 CECR1 (22q11.2) encoding adenosine deaminase 2 have been found. Most cases are sporadic but some familial cases with an autosomal dominant inheritance have been reported. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sneddon syndrome	Is a	Cerebrovascular disease	true	Inferred relationship	Some
Sneddon syndrome	Is a	Livedo reticularis	true	Inferred relationship	Some
Sneddon syndrome	Finding site	Cerebrovascular system structure	true	Inferred relationship	Some	1
Sneddon syndrome	Finding site	Blood vessel structure of skin	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Unit of use size reference set

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3307401018	Livedo reticularis and cerebrovascular accident syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3307402013	Livedo reticularis and cerebrovascular accident syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3307404014	Sneddon syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3307405010	Ehrmann Sneddon syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3307406011	Livedo racemosa and cerebrovascular accident	en	Synonym	Active	Case insensitive	SNOMED CT core
3307407019	A rare non-inflammatory thrombotic vasculopathy predominantly affecting women in young adulthood. Livedo racemosa is a persistent net-like violaceous-cyanotic, mottled discoloration of the skin that is exacerbated by cold or pregnancy. Neurological manifestations include recurrent transient ischemic attacks and infarcts. While about 50% of cases are idiopathic, the disease can be associated with autoimmune diseases like systemic lupus erythematosus and antiphospholipid syndrome. Genetic factors may play a role in the pathogenesis. Loss-of-function mutations in cat eye syndrome chromosome region candidate 1 CECR1 (22q11.2) encoding adenosine deaminase 2 have been found. Most cases are sporadic but some familial cases with an autosomal dominant inheritance have been reported.	en	Definition	Active	Case sensitive	SNOMED CT core
3307408012	A rare non-inflammatory thrombotic vasculopathy predominantly affecting women in young adulthood. Livedo racemosa is a persistent net-like violaceous-cyanotic, mottled discolouration of the skin that is exacerbated by cold or pregnancy. Neurological manifestations include recurrent transient ischaemic attacks and infarcts. While about 50% of cases are idiopathic, the disease can be associated with autoimmune diseases like systemic lupus erythematosus and antiphospholipid syndrome. Genetic factors may play a role in the pathogenesis. Loss-of-function mutations in cat eye syndrome chromosome region candidate 1 CECR1 (22q11.2) encoding adenosine deaminase 2 have been found. Most cases are sporadic but some familial cases with an autosomal dominant inheritance have been reported.	en	Definition	Active	Case sensitive	SNOMED CT core