Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 725408001
SNOMED CT code
| SNOMED code | 725408001 |
|---|---|
| name | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder) |
| synonyms |
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| attributes - group2 | |
| Finding site | Visual structure 49549006 |
| attributes - group1 | |
| Finding site | Cerebellar structure 113305005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Disorder of eye movements 45030009 Strabismus 22066006 Oculomotor apraxia 193662007 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 725408001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 725408001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Hereditary ataxia 763597000 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 725408001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of coordination 298314008 Ataxia 20262006 Cerebellar ataxia 85102008 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 725408001 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 cerebellar ataxia with oculomotor apraxia type 2 725408001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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