1186724002: HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Finding of head and neck region\Head finding (finding)\...
• \Finding of brain\Disorder of brain (disorder)\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disorder of head (disorder)\Disorder of brain (disorder)\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Functional finding\Cognitive function finding (finding)\Impaired cognition (finding)\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Cardiovascular finding\Disorder of cardiovascular system (disorder)\...
• \Cardiovascular system hereditary disorder\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Cerebrovascular disease\Small vessel cerebrovascular disease (disorder)\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cerebrovascular disease\Small vessel cerebrovascular disease (disorder)\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
• \Disease\Mental disorder\Organic mental disorder\Dementia\HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4667451018	HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4667452013	HTRA1-related autosomal dominant cerebral small vessel disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4667453015	HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4667454014	HTRA1-related autosomal dominant cerebral angiopathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4667455010	A rare genetic cerebral small vessel disease characterised by subcortical ischaemic events associated with cognitive decline and gait disturbance with an age of onset typically in the sixth or seventh decade of life. Imaging reveals white matter hyperintensities, status cribrosum, lacunar infarcts and sometimes microbleeds. Extra-neurological manifestations are absent.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4667456011	A rare genetic cerebral small vessel disease characterized by subcortical ischemic events associated with cognitive decline and gait disturbance with an age of onset typically in the sixth or seventh decade of life. Imaging reveals white matter hyperintensities, status cribrosum, lacunar infarcts and sometimes microbleeds. Extra-neurological manifestations are absent.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

Back to Start