21q partial monosomy syndrome 15841002
SNOMED CT code
| SNOMED code | 15841002 |
|---|---|
| name | 21q partial monosomy syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | 21q partial monosomy syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 21 43009003 |
| Associated morphology | Deletion of long arm 64329008 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| Finding site | Chromosome pair 21 43009003 |
| parents | Deletion of part of chromosome 21 726398002 |
| children | 21q22.11q22.12 microdeletion syndrome 787171006 |
| 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 21 70156005 Deletion of part of chromosome 21 726398002 21q partial monosomy syndrome 15841002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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