9p13 microdeletion syndrome 764725008
SNOMED CT code
| SNOMED code | 764725008 |
|---|---|
| name | 9p13 microdeletion syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | 9p13 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 9 13526007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Deletion of short arm 67285006 |
| Finding site | Chromosome pair 9 13526007 |
| parents | Deletion of part of chromosome 9 726379004 |
| 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 9 5051002 Deletion of part of chromosome 9 726379004 9p13 microdeletion syndrome 764725008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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