3q26q27 microdeletion syndrome 778000002
SNOMED CT code
| SNOMED code | 778000002 |
|---|---|
| name | 3q26q27 microdeletion syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | 3q26q27 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| Finding site | Long arm of chromosome 312242007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 3 113355002 |
| 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 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 Deletion of part of long arm of chromosome 3 726370000 3q26q27 microdeletion syndrome 778000002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 3q26q27 microdeletion syndrome 778000002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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