12q24.31-q24.32 deletion syndrome 880086001
SNOMED CT code
| SNOMED code | 880086001 |
|---|---|
| name | 12q24.31-q24.32 deletion syndrome |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | 12q24.31-q24.32 deletion syndrome (disorder) |
| synonyms | 12q24.31-q24.32 deletion syndrome |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 12 17897000 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Long arm of chromosome 312242007 |
| Associated morphology | Partial monosomy 371169004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 12 37535007 Deletion of part of chromosome 12 726382009 Deletion of part of long arm of chromosome 12 726383004 12q24.31-q24.32 deletion syndrome 880086001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 12q24.31-q24.32 deletion syndrome 880086001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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