Monosomy 22 syndrome 787411009
SNOMED CT code
| SNOMED code | 787411009 |
|---|---|
| name | Monosomy 22 syndrome |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Monosomy 22 syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 22 79229009 |
| Associated morphology | Monosomy 86277003 |
| 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 22 70452003 Monosomy 22 syndrome 787411009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Monosomy and deletion from autosome 205627002 Complete monosomy of autosome 726364006 Monosomy 22 syndrome 787411009 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 22 syndrome 787411009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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