MT-ATP6-related mitochondrial spastic paraplegia 778048001
SNOMED CT code
SNOMED code | 778048001 |
---|---|
name | MT-ATP6-related mitochondrial spastic paraplegia |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) |
synonyms |
|
attributes - group3 | |
Clinical course | Progressive 255314001 |
attributes - group1 | |
Finding site | Spinal cord structure 2748008 |
Associated morphology | Degenerative abnormality 107669003 |
attributes - group6 | |
Interprets | Movement 255324009 |
attributes - group2 | |
Finding site | Right lower extremity structure 62175007 |
attributes - group5 | |
Finding site | Left lower extremity structure 32153003 |
attributes - group4 | |
Interprets | Movement observable 363847004 |
Has interpretation | Absent 2667000 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Maternally inherited mitochondrial deoxyribonucleic acid disease 1162975000 MT-ATP6-related mitochondrial spastic paraplegia 778048001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic metabolic disorder 128289001 MT-ATP6-related mitochondrial spastic paraplegia 778048001 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 MT-ATP6-related mitochondrial spastic paraplegia 778048001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 MT-ATP6-related mitochondrial spastic paraplegia 778048001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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