Monosomy 13q14 syndrome 770566002
SNOMED CT code
| SNOMED code | 770566002 |
|---|---|
| name | Monosomy 13q14 syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Monosomy 13q14 syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Long arm of chromosome 312242007 |
| Associated morphology | Partial monosomy 371169004 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 13 55401003 |
| 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 13 17760001 Deletion of part of chromosome 13 726384005 Deletion of long arm of chromosome 13 205630009 Monosomy 13q14 syndrome 770566002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Monosomy 13q14 syndrome 770566002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com