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390936003: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1465114018 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1476249012 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1477210016 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1465114018 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1465114018 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1476249012 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1476249012 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1477210016 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1477210016 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3420481001000118 Zerebrale autosomal-dominante Arteriopathie mit subkortikalen Infarkten und Leukenzephalopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5247441000241113 artériopathie cérébrale autosomique dominante avec infarctus sous-corticaux et leucoencéphalopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5247441000241113 artériopathie cérébrale autosomique dominante avec infarctus sous-corticaux et leucoencéphalopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3420481001000118 Zerebrale autosomal-dominante Arteriopathie mit subkortikalen Infarkten und Leukenzephalopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Is a Cerebrovascular disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Finding site Cerebrovascular system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Due to True Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 3
White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Is a True Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

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