703219008: Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)

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

\Cardiovascular finding\Disorder of cardiovascular system (disorder)\...

\Cardiovascular system hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)

\Cerebrovascular disease\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cerebrovascular disease\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Cerebrovascular disease	true	Inferred relationship	Some
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Cardiovascular system hereditary disorder	true	Inferred relationship	Some
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Finding site	Cerebrovascular system structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3007495019	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3007753010	CARASIL syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3007851017	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3009019010	Maeda syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3009239015	Nemoto disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3866553018	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2152341000172112	syndrome de Maeda	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
2152361000172111	artériopathie cérébrale autosomique récessive avec infarctus sous-cortical et leuco-encéphalopathie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2152351000172114	cerebrale autosomaal recessieve arteriopathie met subcorticale infarcten en leuko-encefalopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2152371000172119	Maeda-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)