Autosomal recessive cerebelloparenchymal disorder type 3 715369006
SNOMED CT code
| SNOMED code | 715369006 |
|---|---|
| name | Autosomal recessive cerebelloparenchymal disorder type 3 |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Autosomal recessive cerebelloparenchymal disorder type 3 (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Cerebellar structure 113305005 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Spinal cord structure 2748008 |
| attributes - group4 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Cerebellar structure 113305005 |
| attributes - group2 | |
| Clinical course | Non-progressive 702322003 |
| 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 Autosomal recessive cerebelloparenchymal disorder type 3 715369006 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Cerebellar disorder 223176004 Dysgenesis of the cerebellum 253171007 Autosomal recessive cerebelloparenchymal disorder type 3 715369006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Congenital non-progressive ataxia 278509004 Autosomal recessive cerebelloparenchymal disorder type 3 715369006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Autosomal recessive cerebelloparenchymal disorder type 3 715369006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive cerebelloparenchymal disorder type 3 715369006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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