716745004: Livedo reticularis and cerebrovascular accident syndrome (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)

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

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)

\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Cerebrovascular disease\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Cardiovascular finding\Blood vessel finding\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)

\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cerebrovascular disease\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)
\Disease\Disorder of soft tissue\Vascular disorder\Vascular disease of the skin\Livedo reticularis\Livedo reticularis and cerebrovascular accident syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core

3307402013 Livedo reticularis and cerebrovascular accident syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3307404014 Sneddon syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3307405010 Ehrmann Sneddon syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3307406011 Livedo racemosa and cerebrovascular accident en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core

2162291000172118 syndrome de livedo reticularis et accidents vasculaires cérébraux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

2162301000172117 syndrome de livedo racemosa et accidents vasculaires cérébraux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

2162321000172112 syndrome de livedo réticulaire et accidents vasculaires cérébraux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

2162311000172119 syndroom van livedo reticularis en cerebrovasculair accident nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

2162331000172110 Sneddon-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)

2162341000172115 syndroom van Sneddon nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Livedo reticularis and cerebrovascular accident syndrome (disorder)	Is a	Cerebrovascular disease	true	Inferred relationship	Some
Livedo reticularis and cerebrovascular accident syndrome (disorder)	Is a	Livedo reticularis	true	Inferred relationship	Some
Livedo reticularis and cerebrovascular accident syndrome (disorder)	Finding site	Cerebrovascular system structure	true	Inferred relationship	Some	1
Livedo reticularis and cerebrovascular accident syndrome (disorder)	Finding site	Blood vessel structure of skin (body structure)	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307402013	Livedo reticularis and cerebrovascular accident syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307404014	Sneddon syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3307405010	Ehrmann Sneddon syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3307406011	Livedo racemosa and cerebrovascular accident	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
2162291000172118	syndrome de livedo reticularis et accidents vasculaires cérébraux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2162301000172117	syndrome de livedo racemosa et accidents vasculaires cérébraux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2162321000172112	syndrome de livedo réticulaire et accidents vasculaires cérébraux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2162311000172119	syndroom van livedo reticularis en cerebrovasculair accident	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2162331000172110	Sneddon-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
2162341000172115	syndroom van Sneddon	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)