774069007: Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Finding of brain\Encephalopathy\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Encephalopathy\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disorder of head\Encephalopathy\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Functional finding\Cognitive function finding\Impaired cognition\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Disorder of head\Encephalopathy\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments
• \Disease\Mental illness\Organic mental disorder\Dementia\PRKAR1B-related neurodegenerative dementia with intermediate filaments

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3727867012	Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3727868019	PRKAR1B-related neurodegenerative dementia with intermediate filaments	en	Synonym	Active	Case sensitive	SNOMED CT core
3727869010	Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3727870011	A rare genetic neurodegenerative disease with characteristics of dementia and mild parkinsonism with poor levodopa response. Presenting clinical manifestations are memory problems, short attention span, disorientation, language impairment, rigidity, bradykinesia, postural instability and behavioural changes including apathy, anxiety and delusions.	en	Definition	Active	Case sensitive	SNOMED CT core
3727871010	A rare genetic neurodegenerative disease with characteristics of dementia and mild parkinsonism with poor levodopa response. Presenting clinical manifestations are memory problems, short attention span, disorientation, language impairment, rigidity, bradykinesia, postural instability and behavioral changes including apathy, anxiety and delusions.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Mental health disorder reference set

Problem/Diagnosis reference set

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