702439002: Agenesis of corpus callosum with peripheral neuropathy (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Andermann syndrome
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Andermann syndrome
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Andermann syndrome
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Andermann syndrome
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Andermann syndrome

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995109016	Agenesis of corpus callosum with polyneuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
2995425015	Charlevoix disease	en	Synonym	Active	Case sensitive	SNOMED CT core
2995604010	Andermann syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2995673017	Agenesis of corpus callosum with peripheral neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
2995850010	Agenesis of corpus callosum with peripheral neuropathy (disorder)	en	Fully specified name	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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