9p24.3 deletion syndrome 890128002
SNOMED CT code
| SNOMED code | 890128002 |
|---|---|
| name | 9p24.3 deletion syndrome |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | 9p24.3 deletion syndrome (disorder) |
| synonyms | 9p24.3 deletion syndrome |
| attributes - group1 | |
| Associated morphology | Partial monosomy 371169004 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 9 13526007 |
| attributes - group2 | |
| Associated morphology | Deletion of short arm 67285006 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 9 13526007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 9p24.3 deletion syndrome 890128002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 9 5051002 Deletion of part of chromosome 9 726379004 Distal monosomy 9p syndrome 763530000 9p24.3 deletion syndrome 890128002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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