Autosomal recessive spastic paraplegia type 43 764736001
SNOMED CT code
| SNOMED code | 764736001 |
|---|---|
| name | Autosomal recessive spastic paraplegia type 43 |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Autosomal recessive spastic paraplegia type 43 (disorder) |
| synonyms | Autosomal recessive spastic paraplegia type 43 |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Spinal cord structure 2748008 |
| attributes - group3 | |
| Clinical course | Progressive 255314001 |
| 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 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive hereditary spastic paraplegia 1187279003 Autosomal recessive spastic paraplegia type 43 764736001 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 Autosomal recessive spastic paraplegia type 43 764736001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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