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

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

\Cardiovascular finding\Disorder of cardiovascular system\...

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

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\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 (disorder)\Cardiovascular system hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system\Cardiovascular system hereditary disorder\Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system\Cerebrovascular disease (disorder)\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 (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Hereditary disorder of nervous system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Cardiovascular system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	Finding site	Cerebrovascular system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	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
3007495019	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character case insensitive (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
3445911001000111	Zerebrale Arteriopathie mit subkortikalen Infarkten und Leukoenzephalopathie, autosomal-rezessiv	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5450781000241114	artériopathie cérébrale autosomique récessive avec infarctus sous-cortical et leuco-encéphalopathie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5450781000241114	artériopathie cérébrale autosomique récessive avec infarctus sous-cortical et leuco-encéphalopathie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3445911001000111	Zerebrale Arteriopathie mit subkortikalen Infarkten und Leukoenzephalopathie, autosomal-rezessiv	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module