Ring chromosome 19 syndrome 765484001
SNOMED CT code
| SNOMED code | 765484001 |
|---|---|
| name | Ring chromosome 19 syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Ring chromosome 19 syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 19 89959003 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Ring chromosome 23345003 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Ring chromosome 1010276004 Ring chromosome 19 syndrome 765484001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 19 79656000 Ring chromosome 19 syndrome 765484001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Ring chromosome 19 syndrome 765484001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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