230250003: Facioscapulohumeral spinal muscular atrophy with sensory loss (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\Facioscapulohumeral spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy with sensory loss
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy with sensory loss
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy with sensory loss
• \Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy with sensory loss
• \Disorder of body system\Neurological disorder\Motor neurone disease\Hereditary motor neuron disease\Spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy\Facioscapulohumeral spinal muscular atrophy with sensory loss

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
345063015	Davidenkow syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
345064014	Facioscapulohumeral spinal muscular atrophy with sensory loss	en	Synonym	Active	Case insensitive	SNOMED CT core
618032015	Facioscapulohumeral spinal muscular atrophy with sensory loss (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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