724770001: Ataxia co-occurrent and due to abetalipoproteinemia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding related to coordination / incoordination\Ataxia\Hereditary ataxia\Ataxia co-occurrent and due to abetalipoproteinaemia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Ataxia co-occurrent and due to abetalipoproteinaemia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Abetalipoproteinaemia\Ataxia co-occurrent and due to abetalipoproteinaemia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Ataxia co-occurrent and due to abetalipoproteinaemia
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary ataxia\Ataxia co-occurrent and due to abetalipoproteinaemia
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipoprotein deficiency disorder\Abetalipoproteinaemia\Ataxia co-occurrent and due to abetalipoproteinaemia

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3445749014	Ataxia co-occurrent and due to abetalipoproteinemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3445750014	Ataxia co-occurrent and due to abetalipoproteinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3445751013	Ataxia co-occurrent and due to abetalipoproteinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3445752018	Ataxia with abetalipoproteinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3445753011	Ataxia with abetalipoproteinaemia	en	Synonym	Active	Case insensitive	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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