Paternal uniparental disomy of chromosome 21 766720000
SNOMED CT code
| SNOMED code | 766720000 |
|---|---|
| name | Paternal uniparental disomy of chromosome 21 |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Paternal uniparental disomy of chromosome 21 (disorder) |
| synonyms | Paternal uniparental disomy of chromosome 21 |
| attributes - group1 | |
| Finding site | Chromosome pair 21 43009003 |
| Associated morphology | Alteration of chromosome structure 41669009 |
| Occurrence | Congenital 255399007 |
| 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 21 70156005 Paternal uniparental disomy of chromosome 21 766720000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Uniparental disomy 726400003 Uniparental disomy of paternal origin 726402006 Paternal uniparental disomy of chromosome 21 766720000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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