Atrophia bulborum hereditaria 15228007
SNOMED CT code
| SNOMED code | 15228007 |
|---|---|
| name | Atrophia bulborum hereditaria |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Atrophia bulborum hereditaria (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Atrophy 13331008 |
| Finding site | Retinal structure 5665001 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Atrophia bulborum hereditaria 15228007 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Atrophia bulborum hereditaria 15228007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Atrophy of globe of eye 1229938006 Atrophic retina 405722004 Atrophia bulborum hereditaria 15228007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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