Autosomal recessive ataxia due to ubiquinone deficiency 725394006
SNOMED CT code
SNOMED code | 725394006 |
---|---|
name | Autosomal recessive ataxia due to ubiquinone deficiency |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Autosomal recessive ataxia due to ubiquinone deficiency (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Cerebellar structure 113305005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Autosomal recessive ataxia due to ubiquinone deficiency 725394006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Hereditary ataxia 763597000 Autosomal recessive ataxia due to ubiquinone deficiency 725394006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Cerebellar ataxia 85102008 Autosomal recessive ataxia due to ubiquinone deficiency 725394006 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 ataxia due to ubiquinone deficiency 725394006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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