5q22.2 deletion syndrome 890124000
SNOMED CT code
SNOMED code | 890124000 |
---|---|
name | 5q22.2 deletion syndrome |
status | active |
date introduced | 2021-01-31 |
fully specified name(s) | 5q22.2 deletion syndrome (disorder) |
synonyms | 5q22.2 deletion syndrome |
attributes - group1 | |
Finding site | Chromosome pair 5 12399004 |
Associated morphology | Partial monosomy 371169004 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Long arm of chromosome 312242007 |
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 5 57361003 Deletion of part of chromosome 5 726372008 Deletion of part of long arm of chromosome 5 726373003 5q22.2 deletion syndrome 890124000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 5q22.2 deletion syndrome 890124000 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.