Spastic paraplegia, optic atrophy, neuropathy syndrome 725139005

SNOMED CT code

SNOMED code

725139005

name

Spastic paraplegia, optic atrophy, neuropathy syndrome

status

active

date introduced

2017-07-31

fully specified name(s)

Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)

synonyms

Spastic paraplegia, optic atrophy, neuropathy syndrome
SPOAN (spastic paraplegia, optic atrophy, neuropathy) syndrome

attributes - group1

Associated morphology

Degenerative abnormality 107669003

Finding site

Spinal cord structure 2748008

attributes - group4

Clinical course

Progressive 255314001

attributes - group2

Finding site

Optic nerve structure 18234004

Associated morphology

Primary atrophy 68616007

attributes - group5

Interprets

Movement 255324009

attributes - group6

Finding site

Left lower extremity structure 32153003

attributes - group7

Finding site

Right lower extremity structure 62175007

attributes - group3

Interprets

Movement observable 363847004

Has interpretation

Absent 2667000

parents

SPOAN and SPOAN-related disorder 789674008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Second cranial nerve finding 106152006
SPOAN and SPOAN-related disorder 789674008
Spastic paraplegia, optic atrophy, neuropathy syndrome 725139005

ancestors

sorted most to least specific

SPOAN and SPOAN-related disorder 789674008
Second cranial nerve finding 106152006
Autosomal recessive hereditary spastic paraplegia 1187279003
Complicated hereditary spastic paraplegia 230261006
Hereditary optic atrophy 26360005
Cranial nerve finding 106150003
Hereditary spastic paraplegia 39912006
Autosomal recessive hereditary disorder 85995004
Primary optic atrophy 21098003
Inherited optic neuropathy 312942003
Hereditary degenerative disease of central nervous system 106018006
Autosomal hereditary disorder 1899006
Spastic paraplegia 192967009
Chronic myelopathy 434371000124108
Chronic paraplegia 698292000
Optic atrophy 76976005
Hereditary disorder of the visual system 363343008
Hereditary disorder of nervous system 363235000
Spastic syndrome 386781001
Chronic nervous system disorder 128283000
Degenerative disease of the central nervous system 80690008
Disorder of optic nerve 77157004
Paraplegia 60389000
Myelopathy 48522003
Hereditary disorder by system 363137000
Disorder of visual pathways 54767005
Complete bilateral paralysis 29188005
Chronic disease 27624003
Degenerative disorder 362975008
Cranial nerve disorder 73013002
Bilateral lower limb paralytic syndrome 609553000
Finding of spinal cord 299733008
Disorder of spinal region 410730009
Hereditary disease 32895009
Disorder of the central nervous system 23853001
Visual system disorder 128127008
Neuropathy 386033004
Paralytic syndrome 29426003
Finding of spinal region 298379008
Disorder of right lower extremity 451421000124102
Disorder of left lower extremity 451431000124104
Disorder of back 33308003
Disorder of nervous system 118940003
Eye / vision finding 118235002
Central nervous system finding 246556002
Genetic disease 782964007
Paralysis 44695005
Finding of back 414252009
Disorder of lower limb 118937003
Movement disorder 60342002
Disorder of body system 362965005
Motor dysfunction 52559000
Finding of lower limb 116312005
Disorder of limb 128605003
Disease 64572001
Motor nervous system finding 106145009
Finding of limb structure 302293008
Finding of movement 298325004
Neurological finding 102957003
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Eye / vision finding 118235002

Second cranial nerve finding 106152006

SPOAN and SPOAN-related disorder 789674008

Spastic paraplegia, optic atrophy, neuropathy syndrome 725139005

SNOMED CT code