Autosomal dominant retinitis pigmentosa 232052009
SNOMED CT code
SNOMED code | 232052009 |
---|---|
name | Autosomal dominant retinitis pigmentosa |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Autosomal dominant retinitis pigmentosa (disorder) |
synonyms | Autosomal dominant retinitis pigmentosa |
attributes - group1 | |
Associated morphology | Dystrophy 4720007 |
Finding site | Retinal structure 5665001 |
parents | |
children | Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant retinitis pigmentosa 232052009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary retinal dystrophy 41799005 Retinitis pigmentosa 28835009 Autosomal dominant retinitis pigmentosa 232052009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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