10q22.3q23.3 microdeletion syndrome 770401007
SNOMED CT code
| SNOMED code | 770401007 |
|---|---|
| name | 10q22.3q23.3 microdeletion syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | 10q22.3q23.3 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Long arm of chromosome 312242007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group2 | |
| Finding site | Chromosome pair 10 56332006 |
| Associated morphology | Partial monosomy 371169004 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Finding site | Chromosome pair 10 56332006 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Deletion of long arm 64329008 |
| parents | 10q partial monosomy 16129004 |
| 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 10 2893009 Deletion of part of chromosome 10 726380001 10q partial monosomy 16129004 10q22.3q23.3 microdeletion syndrome 770401007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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