6p22 microdeletion syndrome 719662000
SNOMED CT code
| SNOMED code | 719662000 |
|---|---|
| name | 6p22 microdeletion syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | 6p22 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Associated morphology | Partial monosomy 371169004 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 6 45202000 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Short arm of chromosome 278145009 |
| 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 6 44710007 Deletion of part of chromosome 6 726374009 Deletion of part of short arm of chromosome 6 726376006 6p22 microdeletion syndrome 719662000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 6p22 microdeletion syndrome 719662000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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