Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia 785301002
SNOMED CT code
| SNOMED code | 785301002 |
|---|---|
| name | Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Childhood 255398004 |
| Finding site | Spinal cord structure 2748008 |
| Associated morphology | Degenerative abnormality 107669003 |
| attributes - group1 | |
| Occurrence | Childhood 255398004 |
| Finding site | Cerebellar structure 113305005 |
| Associated morphology | Degenerative abnormality 107669003 |
| attributes - group3 | |
| Clinical course | Progressive 255314001 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Hereditary ataxia 763597000 Spinocerebellar ataxia 129609000 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia 785301002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Chronic myelopathy 434371000124108 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia 785301002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Chronic brain syndrome 78689005 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia 785301002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia 785301002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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