3p25.3 deletion syndrome 890123006
SNOMED CT code
| SNOMED code | 890123006 |
|---|---|
| name | 3p25.3 deletion syndrome |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | 3p25.3 deletion syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Partial monosomy 371169004 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 3 113355002 |
| attributes - group2 | |
| Associated morphology | Deletion of short arm 67285006 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 3 113355002 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 3p25.3 deletion syndrome 890123006 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 3 13674001 Deletion of part of chromosome 3 726369001 Distal monosomy 3p syndrome 763528002 3p25.3 deletion syndrome 890123006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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