230253001: Bulbospinal neuronopathy (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Bulbospinal neuronopathy
• \Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Bulbospinal neuronopathy
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Bulbospinal neuronopathy
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Bulbospinal neuronopathy
• \Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Spinal muscular atrophy\Bulbospinal neuronopathy
• \Disorder of body system\Neurological disorder\Motor neurone disease\Hereditary motor neuron disease\Spinal muscular atrophy\Bulbospinal neuronopathy

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
345067019	Bulbospinal neuronopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
345068012	Kennedy syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
345069016	X-linked bulbospinal atrophy	en	Synonym	Active	Case sensitive	SNOMED CT core
345070015	Bulbospinal muscular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
618035018	Bulbospinal neuronopathy (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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