Autosomal dominant spastic paraplegia type 17 230263009
SNOMED CT code
| SNOMED code | 230263009 |
|---|---|
| name | Autosomal dominant spastic paraplegia type 17 |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Autosomal dominant spastic paraplegia type 17 (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Spinal cord structure 2748008 |
| attributes - group3 | |
| Finding site | Peripheral nervous system structure 3058005 |
| attributes - group4 | |
| Finding site | Nerve structure 3057000 |
| attributes - group5 | |
| Clinical course | Progressive 255314001 |
| attributes - group8 | |
| Interprets | Movement 255324009 |
| attributes - group6 | |
| Finding site | Right lower extremity structure 62175007 |
| attributes - group7 | |
| Finding site | Left lower extremity structure 32153003 |
| attributes - group2 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Absent 2667000 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Autosomal dominant distal hereditary motor neuropathy 1156837002 Autosomal dominant spastic paraplegia type 17 230263009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant hereditary spastic paraplegia 737227004 Autosomal dominant complex hereditary spastic paraplegia 1259038005 Autosomal dominant spastic paraplegia type 17 230263009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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