2q24 microdeletion syndrome 719658006
SNOMED CT code
| SNOMED code | 719658006 |
|---|---|
| name | 2q24 microdeletion syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | 2q24 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Long arm of chromosome 312242007 |
| Associated morphology | Partial monosomy 371169004 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 2 113354003 |
| Associated morphology | Partial monosomy 371169004 |
| 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 2q24 microdeletion syndrome 719658006 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 2 32299009 Deletion of part of chromosome 2 726366008 Deletion of part of long arm of chromosome 2 726367004 2q24 microdeletion syndrome 719658006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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