SPOAN and SPOAN-related disorder 789674008
SNOMED CT code
SNOMED code | 789674008 |
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name | SPOAN and SPOAN-related disorder |
status | active |
date introduced | 2020-01-31 |
fully specified name(s) | Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Spinal cord structure 2748008 |
Associated morphology | Degenerative abnormality 107669003 |
attributes - group2 | |
Finding site | Optic nerve structure 18234004 |
Associated morphology | Primary atrophy 68616007 |
attributes - group4 | |
Clinical course | Progressive 255314001 |
attributes - group7 | |
Interprets | Movement 255324009 |
attributes - group3 | |
Finding site | Right lower extremity structure 62175007 |
attributes - group6 | |
Finding site | Left lower extremity structure 32153003 |
attributes - group5 | |
Interprets | Movement observable 363847004 |
Has interpretation | Absent 2667000 |
parents |
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children |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Eye / vision finding 118235002 Second cranial nerve finding 106152006 SPOAN and SPOAN-related disorder 789674008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive hereditary spastic paraplegia 1187279003 SPOAN and SPOAN-related disorder 789674008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Spastic syndrome 386781001 Spastic paraplegia 192967009 Hereditary spastic paraplegia 39912006 Complicated hereditary spastic paraplegia 230261006 SPOAN and SPOAN-related disorder 789674008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Inherited optic neuropathy 312942003 Hereditary optic atrophy 26360005 SPOAN and SPOAN-related disorder 789674008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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