770939009: Huntington disease-like 3 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of movement\Movement disorder\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Central nervous system finding\Finding of brain\Encephalopathy\Chronic brain syndrome\Huntington disease-like 3
• \Central nervous system finding\Finding of brain\Encephalopathy\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Central nervous system finding\Finding of brain\Encephalopathy\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Chronic brain syndrome\Huntington disease-like 3
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Encephalopathy\...
• \Chronic brain syndrome\Huntington disease-like 3
• \Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Finding of head region\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Disorder of head\Encephalopathy\...
• \Chronic brain syndrome\Huntington disease-like 3
• \Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Huntington disease-like 3
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Huntington disease-like 3
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Huntington disease-like 3
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Huntington disease-like 3
• \Disease\Disorder of body system\Neurological disorder\System disorder of the nervous system\Disorder presenting primarily with chorea\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Disorder of body system\Neurological disorder\Chronic nervous system disorder\Chronic brain syndrome\Huntington disease-like 3
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Chronic brain syndrome\Huntington disease-like 3
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Disorder of head\Encephalopathy\Chronic brain syndrome\Huntington disease-like 3
• \Disease\Disorder of head\Encephalopathy\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Disorder of head\Encephalopathy\Disorder of basal ganglia\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Movement disorder\Extrapyramidal disease\Huntington disease-like syndrome\Huntington disease-like 3
• \Disease\Chronic disease\Chronic nervous system disorder\Chronic brain syndrome\Huntington disease-like 3

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3703531018	Huntington disease-like 3	en	Synonym	Active	Case sensitive	SNOMED CT core
3703532013	Huntington disease-like 3 (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
3703533015	A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on brain MRI) progressive frontal cortical atrophy and bilateral caudate atrophy.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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