Spastic paraplegia, nephritis, deafness syndrome 733089005
SNOMED CT code
| SNOMED code | 733089005 |
|---|---|
| name | Spastic paraplegia, nephritis, deafness syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Spastic paraplegia, nephritis, deafness syndrome (disorder) |
| synonyms |
|
| attributes - group5 | |
| Clinical course | Progressive 255314001 |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Spinal cord structure 2748008 |
| attributes - group4 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Hearing 47078008 |
| attributes - group9 | |
| Interprets | Movement 255324009 |
| attributes - group3 | |
| Finding site | Right lower extremity structure 62175007 |
| attributes - group8 | |
| Finding site | Left lower extremity structure 32153003 |
| attributes - group2 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Absent 2667000 |
| attributes - group7 | |
| Occurrence | Congenital 255399007 |
| Finding site | Kidney structure 64033007 |
| attributes - group6 | |
| Occurrence | Congenital 255399007 |
| Finding site | Ear structure 117590005 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Decreased hearing 103276001 Spastic paraplegia, nephritis, deafness syndrome 733089005 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 Spastic paraplegia, nephritis, deafness syndrome 733089005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of genitourinary system 128290005 Spastic paraplegia, nephritis, deafness syndrome 733089005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of ear 128297008 Chronic deafness 232325008 Spastic paraplegia, nephritis, deafness syndrome 733089005 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Spastic paraplegia, nephritis, deafness syndrome 733089005 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Spastic paraplegia, nephritis, deafness syndrome 733089005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Spastic paraplegia, nephritis, deafness syndrome 733089005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Spastic paraplegia, nephritis, deafness syndrome 733089005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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