771238004: Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of movement\Movement disorder\Paralytic syndrome\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Finding of movement\Motor dysfunction\Paralysis\Paralytic syndrome\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Eye / vision finding\Visual system disorder\...
• \Hereditary disorder of the visual system\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disorder of eye movements\Neurologic disorder of eye movements\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Neurological finding\Motor nervous system finding\Motor dysfunction\Paralysis\Paralytic syndrome\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye movements\Neurologic disorder of eye movements\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Neurological disorder\Neurologic disorder of eye movements\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Spinal muscular atrophy\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Disorder of body system\Neurological disorder\Motor neurone disease\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal atrophy, ophthalmoplegia, pyramidal syndrome
• \Disease\Movement disorder\Paralytic syndrome\Ophthalmoplegia\Spinal atrophy, ophthalmoplegia, pyramidal syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3705199011	Hamano Tsukamoto syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3705202018	Spinal atrophy, ophthalmoplegia, pyramidal syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3705203011	Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3705200014	A rare bulbospinal muscular atrophy characterised by generalised neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994.	en	Definition	Active	Case sensitive	SNOMED CT core
3705201013	A rare bulbospinal muscular atrophy characterized by generalized neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994.	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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