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

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

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

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

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3007495019 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3007753010 CARASIL syndrome en Synonym Active Case sensitive SNOMED CT core

3007851017 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy en Synonym Active Case insensitive SNOMED CT core

3009019010 Maeda syndrome en Synonym Active Case sensitive SNOMED CT core

3009239015 Nemoto disease en Synonym Active Case sensitive SNOMED CT core

3866553018 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy en Synonym Active Case insensitive SNOMED CT core

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
3007495019	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3007753010	CARASIL syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3007851017	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
3009019010	Maeda syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3009239015	Nemoto disease	en	Synonym	Active	Case sensitive	SNOMED CT core
3866553018	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy	en	Synonym	Active	Case insensitive	SNOMED CT core